| The entire DSpace / Asiakasorganisaatiot / Suomen ympäristökeskus - Julkaisuarkisto / Artikkeleita | 1 / 2023 | 2 / 2023 | 3 / 2023 | 4 / 2023 | 5 / 2023 | 6 / 2023 | 7 / 2023 | 8 / 2023 | 9 / 2023 | 10 / 2023 | 11 / 2023 | 12 / 2023 | Total |
|---|
| 'Sticky' policies : three country cases on long-term commitment and rooting of RE policy goals | 3 |
3 |
9 |
6 |
5 |
9 |
0 |
1 |
0 |
0 |
0 |
0 |
36 |
| (Sub‐)Antarctic endemic cyanobacteria from benthic mats are rare and have restricted geographic distributions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| 25 years of atmospheric and ecosystem measurements in a boreal forest : Seasonal variation and responses to warm and dry years | 18 |
14 |
17 |
17 |
8 |
9 |
7 |
8 |
15 |
22 |
13 |
5 |
153 |
| A carbonate system time series in the Eastern Mediterranean Sea. Two years of high-frequency in-situ observations and remote sensing | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A common agricultural soil test can identify legacy P hotspots in a drainage ditch network | 18 |
11 |
12 |
4 |
20 |
9 |
3 |
0 |
3 |
5 |
4 |
1 |
90 |
| A comparison of model choice strategies for logistic regression | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A comprehensive approach for assessing social flood vulnerability and social flood risk: The case of Denmark | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A conceptual framework for cross-border impacts of climate change | 2 |
7 |
11 |
6 |
7 |
13 |
2 |
0 |
3 |
12 |
9 |
4 |
76 |
| A conceptual framework for responding to cross-border climate change impacts | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A first look into moss living tardigrades in boreal peatlands | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A framework for assessing water security and the water-energy-food nexus : The case of Finland | 6 |
6 |
9 |
6 |
7 |
8 |
1 |
2 |
1 |
0 |
1 |
1 |
48 |
| A geospatial approach for dynamic on-road emission through open-access floating car data | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A global biological conservation horizon scan of issues for 2023 | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
2 |
4 |
4 |
14 |
| A global review and meta-analysis of applications of the freshwater Fish Invasiveness Screening Kit | 3 |
6 |
5 |
4 |
5 |
8 |
2 |
0 |
3 |
2 |
2 |
0 |
40 |
| A horizon scan of global biological conservation issues for 2024 | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A keystone species, European aspen (Populus tremula L.), in boreal forests : Ecological role, knowledge needs and mapping using remote sensing | 20 |
24 |
55 |
25 |
28 |
28 |
21 |
19 |
29 |
30 |
14 |
10 |
303 |
| A Metacommunity Approach to Improve Biological Assessments in Highly Dynamic Freshwater Ecosystems | 2 |
23 |
13 |
2 |
8 |
9 |
1 |
0 |
2 |
1 |
2 |
4 |
67 |
| A methodological guide to observe local‐scale geodiversity for biodiversity research and management | 14 |
27 |
14 |
18 |
21 |
19 |
3 |
2 |
5 |
4 |
7 |
7 |
141 |
| A mire of discount rates : Delaying conservation payment schedules in a choice experiment | 4 |
3 |
9 |
4 |
6 |
7 |
1 |
4 |
3 |
3 |
2 |
1 |
47 |
| A model-based response surface approach for evaluating climate change risks and adaptation urgency | 9 |
7 |
8 |
9 |
9 |
8 |
0 |
3 |
3 |
3 |
4 |
8 |
71 |
| A multi-criteria decision analysis model for ship biofouling management in the Baltic Sea | 13 |
10 |
11 |
7 |
14 |
16 |
9 |
2 |
1 |
2 |
4 |
1 |
90 |
| A new tramway and the formation of emotional commuting experiences | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A parametric method to estimate environmental energy efficiency with non-radial adjustment: an application to China | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A perspective on water quality in connected systems : modelling feedback between upstream and downstream transport and local ecological processes | 9 |
4 |
8 |
5 |
1 |
10 |
1 |
2 |
1 |
1 |
1 |
0 |
43 |
| A power market-based operation support model for sub-daily hydropower regulation practices | 9 |
5 |
8 |
5 |
10 |
6 |
3 |
0 |
2 |
1 |
2 |
6 |
57 |
| A practical approach to improve the statistical performance of surface water monitoring networks | 5 |
2 |
6 |
7 |
5 |
6 |
1 |
1 |
1 |
0 |
0 |
0 |
34 |
| A practical method for evaluating spatial biodiversity offset scenarios based on spatial conservation prioritization outputs | 9 |
0 |
9 |
9 |
10 |
11 |
1 |
1 |
3 |
0 |
0 |
3 |
56 |
| A preliminary study on the ecotoxic potency of wastewater treatment plant sludge combining passive sampling and bioassays | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A retrospective assessment of marine biodiversity : a critical analysis of integration and aggregation rules | 1 |
4 |
7 |
5 |
3 |
8 |
1 |
2 |
1 |
3 |
2 |
3 |
40 |
| A risk management framework for maritime Pollution Preparedness and Response : Concepts, processes and tools | 2 |
2 |
8 |
10 |
15 |
11 |
3 |
1 |
2 |
1 |
1 |
0 |
56 |
| A roadmap for sustaining biodiversity and ecosystem services through joint conservation and restoration of northern drainage basins | 12 |
16 |
17 |
7 |
11 |
9 |
1 |
4 |
2 |
1 |
4 |
2 |
86 |
| A small step toward environmentally sustainable transport? The media debate over the Finnish carbon dioxide-based car tax reform | 4 |
3 |
4 |
4 |
3 |
4 |
1 |
1 |
1 |
0 |
0 |
1 |
26 |
| A socio-technical lens on security in sustainability transitions : Future expectations for positive and negative security | 11 |
9 |
7 |
6 |
8 |
9 |
1 |
3 |
1 |
2 |
2 |
2 |
61 |
| A socio-technical lens on security in sustainability transitions : Future expectations for positive and negative security | 18 |
9 |
6 |
7 |
8 |
9 |
1 |
2 |
3 |
1 |
3 |
2 |
69 |
| A soft clustering approach to detect socio-ecological landscape boundaries using bayesian networks | 3 |
1 |
13 |
5 |
8 |
8 |
0 |
2 |
1 |
0 |
2 |
6 |
49 |
| A spatially explicit comparison of walkability within city-centre and suburban contexts in Helsinki, Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A sustainable blue economy may not be possible in Tanzania without cutting emissions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| A Synthesis of Marine Monitoring Methods With the Potential to Enhance the Status Assessment of the Baltic Sea | 4 |
4 |
7 |
5 |
8 |
8 |
1 |
2 |
3 |
0 |
4 |
1 |
47 |
| A taste for aliens : contribution of a novel prey item to native fishes’ diet | 0 |
1 |
5 |
3 |
6 |
5 |
1 |
0 |
0 |
0 |
2 |
1 |
24 |
| A travel time matrix data set for the Helsinki region 2023 that is sensitive to time, mode and interpersonal differences, and uses open data and novel open-source software | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Abruptly and irreversibly changing Arctic freshwaters urgently require standardized monitoring | 6 |
5 |
10 |
8 |
7 |
8 |
2 |
1 |
0 |
9 |
5 |
1 |
62 |
| Accuracy assessment of remotely sensed data to analyze lake water balance in semi-arid region | 10 |
16 |
16 |
10 |
12 |
11 |
8 |
5 |
0 |
3 |
1 |
3 |
95 |
| Accuracy of Manual Snow Sampling, Depending on the Sampler’s Cross-Section—A Comparative Study | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
1 |
1 |
0 |
5 |
| Achieving social-ecological fit in projectified environmental governance : Exploring vertical and horizontal dimensions | 21 |
11 |
8 |
9 |
9 |
10 |
2 |
3 |
2 |
1 |
2 |
2 |
80 |
| Acid rain and air pollution : 50 years of progress in environmental science and policy | 6 |
4 |
9 |
10 |
17 |
16 |
11 |
9 |
0 |
1 |
4 |
3 |
90 |
| Acoustic Doppler Velocimetry (ADV) data on flow-vegetation interaction with natural-like and rigid model plants in hydraulic flumes | 7 |
5 |
7 |
8 |
10 |
7 |
2 |
1 |
0 |
1 |
0 |
0 |
48 |
| Action-oriented knowledge for sustainable management of organic soils in Finnish agriculture | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
2 |
1 |
2 |
7 |
| Acute aquatic toxicity of arsenic-based chemical warfare agents to Daphnia magna | 10 |
4 |
5 |
4 |
4 |
4 |
0 |
0 |
4 |
2 |
3 |
1 |
41 |
| Adapting Hydropower to European Union Water Law: Flexible Governance versus Legal Effectiveness in Sweden and Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Advanced monitoring of harmful substances and their effects in the Baltic Sea is desired : A comment on Kanwischer et al. (2021) | 4 |
3 |
9 |
7 |
6 |
11 |
1 |
1 |
1 |
0 |
0 |
1 |
44 |
| Advancing the use of molecular methods for routine freshwater macroinvertebrate biomonitoring : the need for calibration experiments | 2 |
7 |
14 |
3 |
6 |
9 |
1 |
2 |
1 |
0 |
1 |
1 |
47 |
| Aesthetics in Biodiversity Conservation | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Agricultural limitations to soil carbon sequestration: Plant growth, microbial activity, and carbon stabilization | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Agricultural water management using two-stage channels : Performance and policy recommendations based on Northern European experiences | 5 |
4 |
6 |
8 |
12 |
9 |
7 |
2 |
2 |
4 |
5 |
0 |
64 |
| Air pollution emission inventory using national high-resolution spatial parameters for the Nordic countries and analysis of PM2.5 spatial distribution for road transport and machinery and off-road sectors | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Air pollution inequality and its temporal trends in Nordic countries | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Air pollution, physical activity and health : A mapping review of the evidence | 7 |
4 |
10 |
11 |
7 |
10 |
2 |
5 |
1 |
3 |
3 |
2 |
65 |
| Airborne DNA reveals predictable spatial and seasonal dynamics of fungi | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Ajantasaista ohjeistusta luontoselvitysten laadintaan ja luontovaikutusten arviointiin | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
4 |
2 |
2 |
9 |
| Alien predation in wetlands : the Raccoon dog and waterbird breeding success | 3 |
12 |
13 |
10 |
14 |
10 |
4 |
5 |
5 |
1 |
1 |
4 |
82 |
| Alternative policy narratives of the future of climate change: Analyzing Finland's energy and climate strategy and news reports | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Alternative proteins and EU food law | 21 |
16 |
11 |
8 |
18 |
6 |
1 |
3 |
7 |
0 |
0 |
1 |
92 |
| Ambitiousness of Sustainable Development Goal (SDG) targets : classification and implications for policy making | 4 |
12 |
8 |
8 |
5 |
11 |
0 |
2 |
0 |
0 |
0 |
2 |
52 |
| An investigation into the ability of three fungi and one yeast to grow and capture nutrients in cheese whey | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| An open web-based GIS service for biomass data in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Analysis of COVID-19 recovery and resilience policy in Finland: a transformative policy mix approach | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
2 |
3 |
3 |
10 |
| Analyzing fair access to urban green areas using multimodal accessibility measures and spatial prioritization | 6 |
5 |
20 |
8 |
11 |
14 |
2 |
5 |
94 |
3 |
6 |
7 |
181 |
| Anthropogenic disturbances alter the relationships between environmental heterogeneity and biodiversity of stream insects | 3 |
9 |
6 |
6 |
8 |
13 |
2 |
2 |
1 |
1 |
1 |
2 |
54 |
| Anthropogenic underwater noise: A review on physiological and molecular responses of marine biota | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Aphyllophoroid funga (Basidiomycota) of Finland : range extensions and records of nationally new and rare species | 11 |
4 |
7 |
3 |
4 |
4 |
3 |
1 |
0 |
0 |
0 |
1 |
38 |
| Applicability and consequences of the integration of alternative models for CO2 transfer velocity into a process-based lake model | 3 |
7 |
6 |
3 |
6 |
6 |
1 |
2 |
2 |
2 |
1 |
1 |
40 |
| Application-based evaluation of multi-basin hydrological models | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Applying a science‐based systems perspective to dispel misconceptions about climate effects of forest bioenergy | 6 |
17 |
14 |
24 |
18 |
12 |
3 |
0 |
0 |
2 |
0 |
1 |
97 |
| Aquatic bryophytes play a key role in sediment-stressed boreal headwater streams | 2 |
4 |
9 |
3 |
3 |
10 |
3 |
2 |
1 |
0 |
3 |
1 |
41 |
| Are people willing to share living space? Household preferences in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Assessing and predicting the influence of chromophoric dissolved organic matter on light absorption by phytoplankton in boreal lakes | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Assessing biodiversity impacts in life cycle assessment framework : Comparing approaches based on species richness and ecosystem indicators in the case of Finnish boreal forests | 10 |
13 |
16 |
17 |
12 |
8 |
8 |
5 |
11 |
16 |
13 |
7 |
136 |
| Assessing critical load exceedances and ecosystem impacts of anthropogenic nitrogen and sulphur deposition at unmanaged forested catchments in Europe | 8 |
4 |
11 |
5 |
3 |
9 |
3 |
2 |
2 |
2 |
0 |
0 |
49 |
| Assessing cryosphere-biosphere linkages in boreal forests with Earth Observation and modelling | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
1 |
2 |
| Assessing mining impacts : The influence of background geochemical conditions on diatom and macroinvertebrate communities in subarctic streams | 3 |
6 |
10 |
5 |
11 |
7 |
2 |
1 |
1 |
1 |
2 |
3 |
52 |
| Assessing the climate impacts of oat straw as a raw material | 8 |
11 |
12 |
4 |
9 |
15 |
4 |
7 |
2 |
6 |
6 |
1 |
85 |
| Assessing the conservation priority of freshwater lake sites based on taxonomic, functional and environmental uniqueness | 15 |
7 |
8 |
12 |
19 |
15 |
25 |
3 |
4 |
8 |
5 |
4 |
125 |
| Assessing the environmental potential of collaborative consumption : Peer-to-peer product sharing in Hammarby Sjöstad, Sweden | 2 |
4 |
5 |
1 |
1 |
1 |
1 |
0 |
1 |
0 |
3 |
2 |
21 |
| Assessing the Potential of Environmental DNA for Monitoring Nature‐Like Bypasses: Erroneous Surveillance Owing to DNA Flow‐Through | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Assessment of ocean color atmospheric correction methods and development of a regional ocean color operational dataset for the Baltic Sea based on Sentinel-3 OLCI | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Association between physical activity and risk of depression | 7 |
8 |
10 |
10 |
18 |
11 |
1 |
9 |
4 |
3 |
3 |
4 |
88 |
| Associations of neighborhood-level socioeconomic status, accessibility, and quality of green spaces in Finnish urban regions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
77 |
5 |
3 |
1 |
86 |
| Assuming accuracy, pretending influence? Risks of measuring, monitoring and reporting sustainable development goals | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
5 |
2 |
2 |
13 |
| Atlas of Finnish bats | 13 |
1 |
13 |
6 |
14 |
26 |
10 |
24 |
21 |
9 |
14 |
11 |
162 |
| Attentive, speculative experimental research for sustainability transitions : An exploration in sustainable eating | 4 |
1 |
9 |
7 |
8 |
10 |
8 |
6 |
3 |
2 |
2 |
2 |
62 |
| Aurinkosähkön pientuotannossa kasvupotentiaalia | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
2 |
1 |
4 |
| Automated detection of boreal forest deadwood using RGB UAV imagery | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
8 |
9 |
| Automatic image-based identification and biomass estimation of invertebrates | 5 |
5 |
8 |
5 |
12 |
9 |
1 |
2 |
0 |
1 |
2 |
1 |
51 |
| Automatic real-time uncertainty estimation for online measurements : a case study on water turbidity | 3 |
3 |
5 |
4 |
4 |
0 |
4 |
0 |
0 |
1 |
0 |
1 |
25 |
| Autonomous mobility justice in the situated Finnish context : A Foucauldian perspective on technology, power, and morality | 9 |
5 |
7 |
6 |
6 |
7 |
2 |
2 |
1 |
0 |
0 |
1 |
46 |
| Autumn to spring microbial community in the northern Baltic Sea : temporal variability in bacterial, viral and nanoflagellate abundance during the cold-water season | 1 |
2 |
6 |
5 |
2 |
8 |
2 |
0 |
1 |
0 |
0 |
0 |
27 |
| Auxiliary datasets improve accuracy of object-based land use/land cover classification in heterogeneous savanna landscapes | 25 |
17 |
21 |
11 |
40 |
20 |
7 |
4 |
9 |
8 |
10 |
7 |
179 |
| Avainbiotooppien merkitys epifyyttijäkälille | 1 |
8 |
10 |
6 |
12 |
5 |
0 |
0 |
0 |
0 |
0 |
0 |
42 |
| Avoiding overly bright future : The systems intelligence perspective on the management of light pollution | 5 |
14 |
4 |
9 |
11 |
11 |
2 |
4 |
4 |
2 |
1 |
4 |
71 |
| Avoimella tiedolla edistetään kestävää yhteiskuntaa | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
3 |
| Bacterial rarity in a subarctic stream network: Biodiversity patterns, assembly mechanisms and types of rarity | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Bacterioplankton dynamics driven by interannual and spatial variation in diatom and dinoflagellate spring bloom communities in the Baltic Sea | 3 |
8 |
4 |
5 |
8 |
3 |
0 |
2 |
1 |
1 |
2 |
4 |
41 |
| Bad nature : Newspaper representations of ecosystem disservices | 4 |
6 |
6 |
7 |
9 |
7 |
2 |
0 |
0 |
1 |
0 |
0 |
42 |
| Balancing profitability of energy production, societal impacts and biodiversity in offshore wind farm design | 6 |
7 |
10 |
10 |
12 |
17 |
26 |
3 |
5 |
5 |
96 |
2 |
199 |
| Balancing urban green space and residential infill development : A spatial multi-criteria approach based on practitioner engagement | 4 |
5 |
10 |
10 |
7 |
9 |
4 |
4 |
7 |
4 |
4 |
0 |
68 |
| Baltic Sea transparency from ships and satellites : centennial trends | 2 |
5 |
8 |
3 |
7 |
5 |
4 |
2 |
3 |
1 |
0 |
0 |
40 |
| Basin-specific changes in filamentous cyanobacteria community composition across four decades in the Baltic Sea | 11 |
6 |
9 |
8 |
9 |
7 |
2 |
1 |
0 |
0 |
0 |
0 |
53 |
| Bayesian calibration and uncertainty quantification for a large nutrient load impact model | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Bayesian Networks in Environmental Risk Assessment : A Review | 7 |
4 |
9 |
2 |
6 |
7 |
7 |
3 |
1 |
0 |
2 |
2 |
50 |
| Beaver-induced spatiotemporal patch dynamics affect landscape-level environmental heterogeneity | 5 |
1 |
8 |
6 |
5 |
10 |
3 |
2 |
2 |
1 |
1 |
4 |
48 |
| Beaver-induced spatiotemporal patch dynamics affect landscape-level environmental heterogeneity | 1 |
5 |
6 |
7 |
9 |
6 |
3 |
1 |
5 |
2 |
1 |
0 |
46 |
| Benefits and challenges of streamlined life-cycle assessment for SMEs : findings from case studies on climate change impacts | 16 |
24 |
15 |
15 |
20 |
25 |
14 |
11 |
22 |
12 |
15 |
6 |
195 |
| Benthic fauna contribute to microplastic sequestration in coastal sediments | 7 |
7 |
15 |
9 |
10 |
13 |
11 |
9 |
3 |
6 |
2 |
2 |
94 |
| Benthic-pelagic coupling and trophic relationships in northern Baltic Sea food webs | 12 |
5 |
6 |
5 |
8 |
14 |
1 |
2 |
0 |
0 |
1 |
0 |
54 |
| Bioclimatic context of species' populations determines community stability | 16 |
9 |
13 |
7 |
13 |
7 |
4 |
6 |
1 |
1 |
1 |
1 |
79 |
| Biocultural diversity (BCD) in European cities – interactions between motivations, experiences and environment in public parks | 37 |
6 |
18 |
15 |
22 |
16 |
4 |
5 |
2 |
5 |
1 |
0 |
131 |
| Biocultural diversity in an urban context : An indicator-based decision support tool to guide the planning and management of green infrastructure | 3 |
4 |
8 |
9 |
5 |
5 |
1 |
0 |
1 |
0 |
1 |
1 |
38 |
| Biodiversiteetin mittaaminen ja uudet menetelmät | 28 |
31 |
27 |
32 |
22 |
15 |
4 |
4 |
13 |
21 |
21 |
7 |
225 |
| Biodiversity and ecosystem services in business sustainability: Toward systematic, value chain‐wide monitoring that aligns with public accounting | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Biodiversity offsetting as a form of depoliticised nature: Social aspects of a pilot project in Lahti, Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Biodiversity patterns of Arctic diatom assemblages in lakes and streams : Current reference conditions and historical context for biomonitoring | 8 |
5 |
7 |
3 |
5 |
6 |
2 |
1 |
0 |
0 |
2 |
4 |
43 |
| Bioflocculation of Euglena gracilis via direct application of fungal filaments : a rapid harvesting method | 6 |
2 |
15 |
7 |
9 |
4 |
2 |
3 |
1 |
1 |
0 |
1 |
51 |
| Biomarker responses and accumulation of polycyclic aromatic hydrocarbons in Mytilus trossulus and Gammarus oceanicus during exposure to crude oil | 7 |
7 |
8 |
2 |
3 |
6 |
0 |
1 |
1 |
0 |
1 |
0 |
36 |
| Biomarker responses in mussels (Mytilus trossulus) from the Baltic Sea exposed to water-accommodated fraction of crude oil and a dispersant at different salinities | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
1 |
0 |
2 |
5 |
| Biotic interactions hold the key to understanding metacommunity organisation | 4 |
4 |
5 |
3 |
5 |
9 |
5 |
0 |
1 |
2 |
1 |
0 |
39 |
| Bioturbation transports secondary microplastics to deeper layers in soft marine sediments of the northern Baltic Sea | 5 |
3 |
4 |
5 |
5 |
1 |
2 |
1 |
0 |
2 |
1 |
0 |
29 |
| Black carbon and inorganic aerosols in Arctic snowpack | 3 |
4 |
5 |
3 |
4 |
6 |
7 |
2 |
4 |
0 |
0 |
0 |
38 |
| Black carbon emissions from flaring in Russia in the period 2012-2017 | 247 |
5 |
7 |
4 |
5 |
13 |
3 |
3 |
7 |
13 |
6 |
5 |
318 |
| Blue bioeconomy localities at the margins : Reconnecting Norwegian seaweed farming and Finnish small-scale lake fisheries with blue policies | 3 |
2 |
12 |
5 |
7 |
13 |
2 |
4 |
1 |
0 |
0 |
1 |
50 |
| Blue consequences of the green bioeconomy : Clear‐cutting intensifies the harmful impacts of land drainage on stream invertebrate biodiversity | 6 |
2 |
13 |
4 |
5 |
8 |
2 |
1 |
2 |
1 |
2 |
1 |
47 |
| Blueprint for a digital twin of a river basin | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
3 |
6 |
| BOBCATSSS 2023 — opiskelijat ja ammattilaiset yhdessä | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
2 |
1 |
5 |
| Boreal peatland forests : ditch network maintenance effort and water protection in a forest rotation framework | 9 |
2 |
5 |
2 |
6 |
15 |
2 |
2 |
3 |
0 |
1 |
0 |
47 |
| Brackish-water benthic fauna under fluctuating environmental conditions : The role of eutrophication, hypoxia, and global change | 3 |
1 |
6 |
7 |
1 |
6 |
1 |
1 |
1 |
0 |
0 |
0 |
27 |
| Bridging the Science-Policy Gap - Toward Better Integration of Decision Support Tools in Coastal and Marine Policy Implementation | 5 |
2 |
8 |
7 |
13 |
9 |
1 |
1 |
0 |
1 |
2 |
1 |
50 |
| Bridging the Science-Policy Gap : Toward Better Integration of Decision Support Tools in Coastal and Marine Policy Implementation | 3 |
4 |
7 |
6 |
5 |
10 |
4 |
1 |
0 |
3 |
0 |
1 |
44 |
| Bringing Back Ecological Flows : Migratory Fish, Hydropower and Legal Maladaptivity in the Governance of Finnish Rivers | 7 |
3 |
6 |
1 |
8 |
7 |
2 |
1 |
3 |
2 |
3 |
1 |
44 |
| Bringing the margin to the focus : 10 challenges for riparian vegetation science and management | 0 |
26 |
17 |
6 |
5 |
14 |
3 |
3 |
1 |
2 |
1 |
1 |
79 |
| Browning from headwaters to coastal areas in the boreal region: Trends and drivers | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Browning of boreal lakes: Do public perceptions and governance align with the biological foundations? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
2 |
3 |
2 |
9 |
| Burning roots : Stakeholder arguments and media representations on the sustainability of tree stump extraction in Finland | 14 |
4 |
6 |
6 |
11 |
11 |
3 |
3 |
1 |
0 |
1 |
2 |
62 |
| Burning wet wood : varieties of non-recognition in energy transitions | 1 |
2 |
1 |
1 |
4 |
5 |
4 |
2 |
0 |
0 |
1 |
2 |
23 |
| Business model innovation in demand response firms : Beyond the niche-regime dichotomy | 5 |
6 |
9 |
6 |
5 |
11 |
5 |
1 |
2 |
0 |
1 |
0 |
51 |
| Butterfly species' responses to urbanization : differing effects of human population density and built-up area | 5 |
2 |
8 |
5 |
14 |
15 |
13 |
22 |
4 |
4 |
7 |
9 |
108 |
| Calibration of in situ chlorophyll fluorometers for organic matter | 9 |
5 |
6 |
8 |
9 |
8 |
3 |
5 |
6 |
4 |
3 |
0 |
66 |
| Campylobacter species, Salmonella serotypes and ribosomal RNA-based fecal source tracking in the Kokemäki River watershed | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Can information from citizen science data be used to predict biodiversity in stormwater ponds? | 7 |
3 |
6 |
3 |
6 |
11 |
3 |
3 |
0 |
0 |
1 |
4 |
47 |
| Can protected areas buffer short-term population changes of resident bird species in a period of intensified forest harvesting? | 3 |
10 |
18 |
3 |
6 |
13 |
2 |
0 |
3 |
8 |
7 |
3 |
76 |
| Can there be water scarcity with abundance of water? : Analyzing water stress during a severe drought in Finland | 6 |
3 |
4 |
3 |
4 |
8 |
1 |
0 |
5 |
1 |
0 |
2 |
37 |
| Can Topographic Variation in Climate Buffer against Climate Change-Induced Population Declines in Northern Forest Birds? | 9 |
2 |
7 |
4 |
15 |
10 |
6 |
1 |
2 |
2 |
1 |
2 |
61 |
| Capability of HYDRUS wetland module to simulate flow and nitrogen removal processes in pilot-scale treatment peatlands under frost and no-frost conditions | 16 |
16 |
11 |
3 |
4 |
6 |
1 |
3 |
2 |
0 |
1 |
0 |
63 |
| Capturing consumers’ awareness and the intention to support carbon neutrality through energy efficient consumption | 4 |
19 |
10 |
5 |
14 |
9 |
5 |
2 |
5 |
16 |
4 |
8 |
101 |
| Carbon and nutrient recycling ecotechnologies in three Baltic Sea river basins : the effectiveness in nutrient load reduction | 7 |
6 |
13 |
2 |
8 |
8 |
2 |
0 |
0 |
1 |
0 |
0 |
47 |
| Carbon Credits Through Wood Use: Revisiting the Maximum Potential and Sensitivity to Key Assumptions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Carbon handprint – a review of potential climate benefits of buildings | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Carbon neutral higher education institutions: a reality check, challenges and solutions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Carbon sequestration and storage potential of urban residential environment – A review | 24 |
19 |
13 |
11 |
22 |
11 |
6 |
16 |
51 |
4 |
11 |
7 |
195 |
| Care-full research ethics in multispecies relations on dairy farms | 11 |
6 |
6 |
8 |
10 |
14 |
2 |
3 |
3 |
0 |
1 |
2 |
66 |
| Catchment and lake network modify export of anaerobic oxidation capacity in boreal freshwaters | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
2 |
6 |
| Catchment effects of a future Nordic bioeconomy : From land use to water resources | 6 |
1 |
10 |
4 |
9 |
6 |
1 |
3 |
1 |
0 |
0 |
1 |
42 |
| Catchment properties and the photosynthetic trait composition of freshwater plant communities | 2 |
3 |
11 |
4 |
5 |
7 |
1 |
1 |
0 |
0 |
0 |
0 |
34 |
| Causal approach to environmental risks of seabed mining | 9 |
8 |
9 |
5 |
72 |
10 |
3 |
19 |
3 |
2 |
3 |
5 |
148 |
| Century-long butterfly range expansions in northern Europe depend on climate, land use and species traits | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
6 |
1 |
2 |
2 |
11 |
| Challenges and solutions in developing legitimate online participation for EU biodiversity and ecosystem services policies | 6 |
2 |
7 |
2 |
9 |
7 |
5 |
1 |
1 |
1 |
0 |
0 |
41 |
| Change in beta diversity of riverine fish during and after supra-seasonal drought | 3 |
18 |
7 |
7 |
10 |
10 |
3 |
5 |
3 |
1 |
4 |
4 |
75 |
| Changes in biomass and diversity of soil macrofauna along a climatic gradient in European boreal forests | 10 |
20 |
5 |
5 |
7 |
12 |
1 |
1 |
0 |
0 |
0 |
0 |
61 |
| Changes in macrofaunal biological traits across estuarine gradients : implications for the coastal nutrient filter | 11 |
5 |
6 |
7 |
12 |
8 |
3 |
3 |
4 |
2 |
4 |
1 |
66 |
| Changes in the discharge regime of Finnish rivers | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Changes in the functional features of macrophyte communities and driving factors across a 70-year period | 7 |
6 |
8 |
3 |
12 |
9 |
1 |
1 |
4 |
1 |
3 |
1 |
56 |
| Changing Winters and Adaptive Water Governance: A Case Study on the Kemi River Basin, Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
1 |
1 |
1 |
6 |
| Characteristics, main impacts, and stewardship of natural and artificial freshwater environments : Consequences for biodiversity conservation | 9 |
7 |
25 |
11 |
5 |
10 |
2 |
2 |
4 |
1 |
2 |
3 |
81 |
| Chemical leaching from polyethylene mulching films to soil in strawberry farming | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
2 |
1 |
2 |
7 |
| Choosing reference land use for carbon and biodiversity footprints | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Chronic oral exposure to Amistar fungicide does not significantly affect colour discrimination but may impact memory retention in bumblebees | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
6 |
0 |
4 |
4 |
14 |
| Circular bioeconomy : Actors and dynamics of knowledge co-production in Finland | 21 |
11 |
9 |
3 |
13 |
13 |
2 |
3 |
2 |
1 |
0 |
4 |
82 |
| Circular economy in wastewater management : The potential of source-separating sanitation in rural and peri-urban areas of Northern Finland and Sweden | 4 |
3 |
14 |
28 |
19 |
9 |
8 |
16 |
4 |
5 |
3 |
2 |
115 |
| Circular economy policies and their transformative outcomes : The transformative intent of Finland's strategic policy programme | 3 |
15 |
13 |
10 |
10 |
18 |
8 |
14 |
12 |
14 |
7 |
7 |
131 |
| Circular economy solutions for magnetic resonance imaging–Mitigation of environmental impacts and critical raw material use | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Circular nutrient solutions for agriculture and wastewater : a review of technologies and practices | 0 |
25 |
21 |
9 |
8 |
11 |
3 |
3 |
4 |
2 |
1 |
1 |
88 |
| Circulation patterns in the Gulf of Finland from daily to seasonal timescales | 2 |
5 |
13 |
9 |
13 |
16 |
3 |
5 |
10 |
35 |
5 |
5 |
121 |
| Circumpolar patterns of Arctic freshwater fish biodiversity : A baseline for monitoring | 3 |
10 |
10 |
7 |
6 |
5 |
2 |
1 |
0 |
0 |
0 |
1 |
45 |
| Circumpolar patterns of Arctic freshwater fish biodiversity : A baseline for monitoring | 4 |
5 |
8 |
8 |
5 |
5 |
2 |
1 |
3 |
1 |
3 |
0 |
45 |
| Cities as carbon sinks : Classification of wooden buildings | 8 |
9 |
18 |
4 |
16 |
14 |
7 |
4 |
2 |
3 |
2 |
2 |
89 |
| Citizen beliefs concerning wood as a construction material under extreme weather events | 8 |
6 |
10 |
7 |
11 |
9 |
3 |
3 |
2 |
1 |
1 |
4 |
65 |
| Citizen energy lost in sustainability transitions: Knowledge co-production in a complex governance context | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
3 |
5 |
| Citizen science and environmental protection agencies : engaging citizens to address key environmental challenges | 0 |
2 |
7 |
4 |
9 |
7 |
4 |
1 |
1 |
0 |
0 |
1 |
36 |
| Citizen science provides added value in the monitoring for coastal non-indigenous species | 0 |
23 |
11 |
6 |
6 |
9 |
3 |
3 |
2 |
1 |
2 |
1 |
67 |
| Citizens’ images of a sustainable energy transition | 3 |
4 |
11 |
12 |
10 |
16 |
3 |
2 |
4 |
4 |
2 |
4 |
75 |
| Citizens’ sustainable, future-oriented energy behaviours in energy transition | 16 |
2 |
15 |
13 |
15 |
14 |
2 |
1 |
5 |
5 |
3 |
3 |
94 |
| Clean air policies are key for successfully mitigating Arctic warming | 7 |
10 |
10 |
6 |
8 |
7 |
5 |
2 |
2 |
0 |
1 |
1 |
59 |
| Cleaning up seas using blue growth initiatives : Mussel farming for eutrophication control in the Baltic Sea | 0 |
20 |
14 |
4 |
6 |
6 |
5 |
4 |
6 |
9 |
3 |
2 |
79 |
| Climate and land-use change drive population decline in a red-listed plant species | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
1 |
2 |
| Climate change adaptation in water law: International, EU and Finnish perspectives | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Climate change and mercury in the Arctic : Abiotic interactions | 7 |
13 |
10 |
12 |
12 |
8 |
2 |
2 |
1 |
0 |
6 |
4 |
77 |
| Climate change in the Baltic Sea region : a summary | 4 |
11 |
4 |
8 |
12 |
15 |
9 |
3 |
8 |
16 |
18 |
24 |
132 |
| Climate change mitigation potential of paludiculture in Finland: greenhouse gas emissions of abandoned organic croplands and peat substitution | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Climate change reshuffles northern species within their niches | 8 |
9 |
11 |
11 |
11 |
11 |
6 |
9 |
24 |
73 |
8 |
2 |
183 |
| Climate impact of Finnish air pollutants and greenhouse gases using multiple emission metrics | 4 |
7 |
9 |
5 |
11 |
17 |
6 |
7 |
4 |
0 |
0 |
2 |
72 |
| Climate risks to the renewable energy sector: Assessment and adaptation within energy companies | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Climate security connects fragile and strong states via cascading effects : A review essay | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Climate Security Connects Fragile and Strong States via Cascading Effects: A Review Article | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Climate targets in European timber-producing countries conflict with goals on forest ecosystem services and biodiversity | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
0 |
2 |
4 |
| Climate, Hydrology, and Nutrients Control the Seasonality of Si Concentrations in Rivers | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Climate-driven deoxygenation of northern lakes | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Closing an open balance : The impact of increased tree harvest on forest carbon | 6 |
7 |
12 |
10 |
8 |
12 |
5 |
9 |
5 |
3 |
2 |
3 |
82 |
| Co-constructing inclusive knowledge within converging fields : Environmental governance and health care | 3 |
1 |
7 |
3 |
2 |
2 |
0 |
1 |
0 |
0 |
1 |
0 |
20 |
| Co-creating urban ecosystem accounting: Physical and monetary accounts of runoff retention service provided by urban green spaces | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Co-occurrence, ecological profiles and geographical distribution based on unique molecular identifiers of the common freshwater diatoms Fragilaria and Ulnaria | 7 |
4 |
12 |
35 |
14 |
16 |
1 |
1 |
0 |
1 |
3 |
2 |
96 |
| Codified and reflexive policy coordination: how successful are Dhaka City’s policies for a successful sustainable passenger transport transition? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Coincidence of High Nature Value farmlands with bird and butterfly diversity | 58 |
21 |
16 |
8 |
9 |
9 |
2 |
2 |
3 |
0 |
5 |
7 |
140 |
| Collaborative multi-robot search and rescue : Planning, coordination, perception, and active vision | 16 |
1 |
15 |
15 |
9 |
9 |
3 |
20 |
38 |
25 |
8 |
2 |
161 |
| Combined effects of human pressures on Europe’s marine ecosystems | 4 |
3 |
11 |
14 |
10 |
11 |
0 |
1 |
1 |
1 |
1 |
0 |
57 |
| Combined use of satellite image analysis, land-use statistics, and land-use-specific export coefficients to predict nutrients in drained peatland catchment | 6 |
7 |
6 |
2 |
3 |
6 |
1 |
1 |
1 |
143 |
0 |
1 |
177 |
| Combining range and phenology shifts offers a winning strategy for boreal Lepidoptera | 2 |
2 |
5 |
6 |
7 |
1 |
2 |
1 |
1 |
0 |
0 |
0 |
27 |
| Combining spatial prioritization and expert knowledge facilitates effectiveness of large-scale mire protection process in Finland | 12 |
11 |
7 |
9 |
8 |
10 |
11 |
9 |
4 |
2 |
2 |
4 |
89 |
| Communicating sustainability under increasing public budget constraints | 10 |
4 |
2 |
6 |
7 |
5 |
1 |
2 |
1 |
1 |
3 |
3 |
45 |
| Community size can affect the signals of ecological drift and niche selection on biodiversity | 26 |
8 |
14 |
11 |
16 |
24 |
14 |
3 |
1 |
2 |
6 |
3 |
128 |
| Comparing economic and biological management objectives in the commercial Baltic salmon fisheries | 4 |
0 |
11 |
3 |
9 |
10 |
7 |
2 |
2 |
2 |
2 |
1 |
53 |
| Comparing landscape value patterns between participatory mapping and geolocated social media content across Europe | 17 |
13 |
11 |
14 |
11 |
13 |
13 |
129 |
1 |
1 |
0 |
0 |
223 |
| Comparing nutrient reference concentrations in Nordic countries with focus on lowland rivers | 0 |
13 |
12 |
8 |
6 |
7 |
2 |
2 |
0 |
2 |
2 |
0 |
54 |
| Comparison of biological and ecological long-term trends related to northern hemisphere climate in different marine ecosystems | 11 |
4 |
8 |
5 |
7 |
9 |
3 |
0 |
0 |
0 |
0 |
1 |
48 |
| Comparison of Diatoms and Dinoflagellates from Different Habitats as Sources of PUFAs | 5 |
2 |
7 |
4 |
12 |
5 |
2 |
3 |
1 |
0 |
0 |
0 |
41 |
| Complementarity and sensitivity of benthic state indicators to bottom-trawl fishing disturbance | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Complementary use of the ecosystem service concept and multi-criteria decision analysis in water management | 10 |
5 |
14 |
6 |
12 |
13 |
3 |
2 |
4 |
2 |
2 |
0 |
73 |
| Complex plant quality—microbiota–population interactions modulate the response of a specialist herbivore to the defence of its host plant | 22 |
14 |
12 |
5 |
8 |
9 |
5 |
0 |
4 |
2 |
2 |
3 |
86 |
| Composition of natural phytoplankton community has minor effects on autochthonous dissolved organic matter characteristics | 8 |
11 |
11 |
17 |
17 |
9 |
5 |
3 |
4 |
2 |
5 |
10 |
102 |
| Concentration of organic carbon in Finnish catchments and variables involved in its variations | 1 |
14 |
10 |
13 |
7 |
8 |
1 |
2 |
2 |
1 |
1 |
1 |
61 |
| Conceptual mini-catchment typologies for testing dominant controls of nutrient dynamics in three Nordic Countries | 3 |
7 |
7 |
7 |
5 |
9 |
2 |
2 |
2 |
0 |
0 |
0 |
44 |
| Consistency in microbiomes in cultures of Alexandrium species isolated from brackish and marine waters | 1 |
3 |
4 |
2 |
7 |
3 |
1 |
0 |
0 |
1 |
0 |
1 |
23 |
| Consistency of impact assessment protocols for non-native species | 6 |
6 |
13 |
6 |
5 |
11 |
3 |
1 |
4 |
2 |
4 |
1 |
62 |
| Consistency of targeted metatranscriptomics and morphological characterization of phytoplankton communities | 9 |
6 |
11 |
5 |
8 |
9 |
6 |
2 |
2 |
3 |
1 |
122 |
184 |
| Consumer preferences for recycled plastics : Observations from a citizen survey | 25 |
16 |
10 |
17 |
26 |
21 |
4 |
3 |
5 |
6 |
2 |
2 |
137 |
| Consumption-based emission inventories in Nordic municipalities—a quest to develop support for local climate action | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Contaminated by war : A brief history of sea-dumping of munitions | 0 |
17 |
11 |
7 |
6 |
4 |
3 |
1 |
5 |
1 |
2 |
2 |
59 |
| Continuing long-term expansion of low-oxygen conditions in the Eastern Gulf of Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Contrasting distribution and speciation of sedimentary organic phosphorus among different basins of the Baltic Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
3 |
1 |
1 |
9 |
| Contrasting latitudinal patterns in diversity and stability in a high-latitude species-rich moth community | 6 |
2 |
27 |
6 |
7 |
6 |
1 |
3 |
3 |
5 |
0 |
4 |
70 |
| Contributing factors for electricity storage in a carbon‐free power system | 2 |
3 |
14 |
10 |
7 |
8 |
2 |
3 |
4 |
0 |
0 |
3 |
56 |
| Contribution of flow conditions and sand addition on hyporheic zone exchange in gravel beds | 7 |
4 |
4 |
6 |
5 |
12 |
3 |
0 |
0 |
1 |
0 |
3 |
45 |
| Contributions to the knowledge of aphyllophoroid and heterobasidioid funga (Basidiomycota) in Finland | 2 |
2 |
10 |
9 |
6 |
9 |
2 |
3 |
3 |
0 |
1 |
3 |
50 |
| Coordination of water policies for quality and quantity : experiences from Nordic and Baltic countries | 11 |
8 |
9 |
7 |
6 |
9 |
7 |
2 |
1 |
0 |
1 |
3 |
64 |
| Cormorant predation mortality of perch (Perca fluviatilis) in coastal and archipelago areas, northern Baltic Sea | 7 |
7 |
5 |
8 |
14 |
8 |
0 |
5 |
0 |
0 |
1 |
0 |
55 |
| Corporate Engagement in Water Policy and Governance: A Literature Review on Water Stewardship and Water Security | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Correlates of different facets and components of betadiversity in stream organisms | 2 |
1 |
5 |
2 |
7 |
8 |
0 |
1 |
1 |
3 |
0 |
0 |
30 |
| Cost-effective biodiversity protection through multiuse-conservation landscapes | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Cost-efficiency assessments of marine monitoring methods lack rigor : a systematic mapping of literature and an end-user view on optimal cost-efficiency analysis | 2 |
5 |
3 |
3 |
5 |
2 |
0 |
0 |
2 |
0 |
1 |
1 |
24 |
| Creating collaboration for contentious projects on managed aquifer recharge : two cases from Finland | 2 |
2 |
6 |
4 |
6 |
7 |
2 |
2 |
0 |
0 |
0 |
1 |
32 |
| Crop type rather than production method determines functional trait composition of insect communities on arable land in boreal agricultural landscapes | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Cross-realm transferability of species distribution models–Species characteristics and prevalence matter more than modelling methods applied | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Cross-sectional associations of neighbourhood socioeconomic disadvantage and greenness with accelerometer-measured leisure-time physical activity in a cohort of ageing workers | 2 |
6 |
8 |
4 |
8 |
13 |
1 |
3 |
0 |
0 |
0 |
0 |
45 |
| Cross-sectional associations of neighbourhood socioeconomic disadvantage and greenness with accelerometer-measured leisure-time physical activity in a cohort of ageing workers | 0 |
0 |
5 |
3 |
4 |
10 |
0 |
1 |
1 |
2 |
1 |
3 |
30 |
| Cross‐border dimensions of Arctic climate change impacts and implications for Europe | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Current uncertainties and challenges of publicly available pharmaceutical environmental risk assessment data | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Cutting edge : A comparison of contemporary practices of riparian buffer retention around small streams in Canada, Finland, and Sweden | 3 |
8 |
8 |
17 |
7 |
5 |
2 |
1 |
1 |
8 |
5 |
6 |
71 |
| Cyanobacterial akinete distribution, viability, and cyanotoxin records in sediment archives from the Northern Baltic Sea | 5 |
1 |
5 |
1 |
7 |
7 |
4 |
0 |
5 |
3 |
2 |
3 |
43 |
| Cycling behaviour in 17 countries across 6 continents : levels of cycling, who cycles, for what purpose, and how far? | 15 |
5 |
10 |
9 |
11 |
11 |
10 |
3 |
7 |
16 |
11 |
6 |
114 |
| Daily gridded evapotranspiration data for Finland for 1981–2020 | 0 |
20 |
17 |
13 |
16 |
8 |
1 |
2 |
1 |
2 |
3 |
4 |
87 |
| Dangerous relationships : Biases in freshwater bioassessment based on observed to expected ratios | 8 |
5 |
10 |
8 |
6 |
11 |
3 |
2 |
1 |
1 |
4 |
2 |
61 |
| Dark side of resilience: systemic unsustainability | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
11 |
6 |
3 |
22 |
| Data fusion system for monitoring water quality : Application to chlorophyll-a in Baltic sea coast | 21 |
27 |
11 |
18 |
16 |
13 |
12 |
6 |
2 |
4 |
5 |
2 |
137 |
| Data integration and participatory process in developing integrated coastal zone management (ICZM) in the northern Baltic Sea | 3 |
12 |
10 |
6 |
11 |
11 |
4 |
1 |
3 |
1 |
3 |
2 |
67 |
| Data on different types of green spaces and their accessibility in the seven largest urban regions in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
14 |
3 |
1 |
20 |
| Data summarizing monitoring and evaluation for three European environmental policies in 9 cases across Europe | 6 |
7 |
8 |
3 |
7 |
6 |
1 |
2 |
1 |
0 |
1 |
0 |
42 |
| Data-driven model of the local wind field over two small lakes in Jyväskylä, Finland | 1 |
4 |
1 |
2 |
5 |
3 |
2 |
3 |
1 |
1 |
1 |
4 |
28 |
| Dataset from a mesocosm experiment on brownification in the Baltic Sea | 22 |
13 |
11 |
5 |
7 |
16 |
1 |
8 |
1 |
2 |
0 |
2 |
88 |
| Decision Support Indicators (DSIs) and their role in hydrological planning | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Decision-support tools used in the Baltic Sea area : performance and end-user preferences | 2 |
3 |
3 |
2 |
6 |
5 |
1 |
1 |
4 |
1 |
2 |
3 |
33 |
| Decision-Support Tools Used in the Baltic Sea Area: Performance and End-User Preferences | 3 |
3 |
7 |
2 |
10 |
8 |
1 |
2 |
0 |
1 |
1 |
0 |
38 |
| Declining calcium concentration drives shifts toward smaller and less nutritious zooplankton in northern lakes | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Decolonization of care through a wholistic way of living : Gaga from the Tayal in Taiwan | 5 |
9 |
11 |
7 |
18 |
44 |
5 |
6 |
1 |
4 |
0 |
5 |
115 |
| Decreased surface and bottom salinity and elevated bottom temperature in the Northern Baltic Sea over the past six decades | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
5 |
3 |
2 |
5 |
15 |
| Decreasing snow cover alters functional composition and diversity of Arctic tundra | 9 |
6 |
11 |
7 |
16 |
9 |
2 |
0 |
1 |
0 |
1 |
0 |
62 |
| Deeper waters are changing less consistently than surface waters in a global analysis of 102 lakes | 5 |
8 |
17 |
8 |
12 |
9 |
0 |
1 |
4 |
104 |
2 |
9 |
179 |
| Degradation rates and bacterial community compositions vary among commonly used bioplastic materials in a brackish marine environment | 0 |
0 |
0 |
20 |
21 |
33 |
4 |
87 |
3 |
3 |
5 |
3 |
179 |
| Degradation rates of aged petroleum hydrocarbons are likely to be mass transfer dependent in the field | 12 |
6 |
6 |
15 |
13 |
12 |
3 |
5 |
2 |
6 |
4 |
2 |
86 |
| Delineating the geographic context of physical activities: A systematic search and scoping review of the methodological approaches used in social ecological research over two decades | 2 |
3 |
16 |
15 |
16 |
18 |
10 |
2 |
1 |
2 |
5 |
4 |
94 |
| Depletion of oxygen in the Bothnian Sea since the mid-1950s | 6 |
8 |
8 |
9 |
14 |
8 |
9 |
4 |
6 |
13 |
15 |
14 |
114 |
| Detecting european aspen (Populus tremula L.) in boreal forests using airborne hyperspectral and airborne laser scanning data | 6 |
5 |
8 |
12 |
12 |
10 |
0 |
0 |
1 |
2 |
2 |
1 |
59 |
| Detecting European Aspen (Populus tremula L.) in Boreal Forests Using Airborne Hyperspectral and Airborne Laser Scanning Data | 11 |
4 |
11 |
4 |
14 |
10 |
2 |
2 |
6 |
2 |
1 |
4 |
71 |
| Detecting mining impacts on freshwater ecosystems using replicated sampling before and after the impact | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Detection of European Aspen (Populus tremula L.) Based on an Unmanned Aerial Vehicle Approach in Boreal Forests | 3 |
3 |
13 |
9 |
14 |
8 |
3 |
0 |
3 |
4 |
4 |
8 |
72 |
| Determinants of supplementary heating system choices and adoption consideration in Finland | 1 |
5 |
3 |
4 |
4 |
0 |
3 |
1 |
3 |
3 |
2 |
0 |
29 |
| Determining sectoral and regional sensitivity to climate and socio-economic change in Europe using impact response surfaces | 7 |
8 |
10 |
7 |
7 |
8 |
5 |
2 |
2 |
3 |
1 |
2 |
62 |
| Developing a Multi-sensory Public Participation GIS (MSPPGIS) method for integrating landscape values and soundscapes of urban green infrastructure | 19 |
18 |
31 |
18 |
29 |
6 |
0 |
1 |
1 |
2 |
1 |
3 |
129 |
| Developing fine‐grained nationwide predictions of valuable forests using biodiversity indicator bird species | 9 |
19 |
11 |
5 |
12 |
16 |
1 |
1 |
1 |
0 |
2 |
2 |
79 |
| Developing key indicators of green growth | 4 |
9 |
10 |
8 |
16 |
12 |
0 |
0 |
2 |
1 |
1 |
3 |
66 |
| Developing Policy Pathways : Redesigning Transition Arenas for Mid-Range Planning | 9 |
2 |
11 |
5 |
13 |
12 |
8 |
6 |
2 |
3 |
3 |
3 |
77 |
| Developing together: the Finnish way of promoting sustainable public procurement | 0 |
0 |
0 |
30 |
35 |
16 |
3 |
5 |
3 |
4 |
1 |
2 |
99 |
| Development and application of reference and routine analytical methods providing SI-traceable results for the determination of technology-critical elements in PCB from WEEE | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Development of aerial photos and LIDAR data approaches to map spatial and temporal evolution of ditch networks in peat-dominated catchments | 6 |
10 |
16 |
5 |
8 |
10 |
3 |
6 |
2 |
2 |
1 |
4 |
73 |
| Diatom-mediated food web functioning under ocean artificial upwelling | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Diazotrophic cyanobacteria in planktonic food webs | 5 |
3 |
18 |
6 |
8 |
5 |
4 |
2 |
2 |
0 |
0 |
0 |
53 |
| Different pathways to a recycling society – Comparison of the transitions in Austria, Sweden and Finland | 8 |
14 |
11 |
8 |
12 |
3 |
3 |
1 |
1 |
3 |
0 |
1 |
65 |
| Different regulatory approaches to enhanced water protection in selected European jurisdictions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
3 |
8 |
12 |
| Different responses of taxonomic and functional structures of stream macroinvertebrate communities to local stressors and regional factors in a subtropical biodiversity hotspot | 20 |
9 |
11 |
16 |
14 |
20 |
9 |
3 |
3 |
9 |
1 |
3 |
118 |
| Different responses to artificial ventilation in two stratified coastal basins | 5 |
4 |
9 |
5 |
7 |
8 |
3 |
1 |
0 |
0 |
0 |
0 |
42 |
| Digitalisation in wind and solar power technologies | 11 |
5 |
18 |
16 |
9 |
11 |
4 |
3 |
15 |
7 |
1 |
5 |
105 |
| Discovery of Eremiobacterota with nifH homologues in tundra soil | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Disentangling the effects of dispersal mode on the assembly of macroinvertebrate assemblages in a heterogeneous highland region | 12 |
8 |
5 |
10 |
12 |
10 |
4 |
7 |
4 |
7 |
11 |
41 |
131 |
| Disparities in nutritional adequacy of diets between different socioeconomic groups of Finnish adults | 6 |
4 |
7 |
4 |
13 |
7 |
1 |
158 |
1 |
2 |
1 |
1 |
205 |
| DISPERSE, a trait database to assess the dispersal potential of European aquatic macroinvertebrates | 0 |
16 |
11 |
8 |
4 |
6 |
1 |
0 |
2 |
1 |
1 |
2 |
52 |
| Disservices of urban trees | 12 |
6 |
24 |
30 |
25 |
31 |
1 |
3 |
3 |
5 |
4 |
0 |
144 |
| Distance decay 2.0 – A global synthesis of taxonomic and functional turnover in ecological communities | 12 |
14 |
10 |
15 |
14 |
9 |
4 |
4 |
2 |
0 |
0 |
2 |
86 |
| Distinct healthy and atopic canine gut microbiota is influenced by diet and antibiotics | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
6 |
2 |
8 |
| Distribution and species composition of red algal communities in the northern Baltic Sea | 3 |
14 |
16 |
8 |
9 |
13 |
2 |
3 |
1 |
0 |
1 |
1 |
71 |
| Distribution of microplastics between ice and water in aquatic systems: The influence of particle properties, salinity and freshwater characteristics | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Distribution of perfluoroalkyl acids in fish species from the Baltic Sea and freshwaters in Finland | 7 |
14 |
11 |
8 |
10 |
12 |
4 |
4 |
3 |
5 |
4 |
4 |
86 |
| Do different agronomic soil tests identify similar nutrient deficiencies? | 4 |
3 |
7 |
3 |
4 |
5 |
2 |
1 |
1 |
0 |
0 |
0 |
30 |
| Do hazardous substances in demolition waste hinder circular economy? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Do the ecological drivers of lake littoral communities match and lead to congruence between organism groups? | 5 |
1 |
7 |
7 |
5 |
9 |
2 |
3 |
1 |
0 |
2 |
0 |
42 |
| Does catchment geodiversity foster stream biodiversity? | 3 |
4 |
19 |
34 |
13 |
12 |
6 |
0 |
3 |
2 |
3 |
2 |
101 |
| Does conservation in Natura 2000 areas promote water quality improvement? Findings from a contingent valuation study on environmental benefits and residents’ preferences | 10 |
14 |
13 |
7 |
10 |
10 |
2 |
1 |
6 |
2 |
5 |
6 |
86 |
| Down with the flow : public debates shaping the risk framing of artificial groundwater recharge | 4 |
4 |
4 |
5 |
9 |
7 |
2 |
0 |
2 |
0 |
0 |
0 |
37 |
| Drainage for forestry increases N, P and TOC export to boreal surface waters | 5 |
9 |
12 |
5 |
16 |
12 |
0 |
2 |
0 |
4 |
1 |
0 |
66 |
| Drivers of household consumption expenditure and carbon footprints in Finland | 5 |
6 |
12 |
26 |
19 |
15 |
3 |
80 |
6 |
1 |
4 |
4 |
181 |
| Drought Assessment in São Francisco River Basin, Brazil : Characterization through SPI and Associated Anomalous Climate Patterns | 4 |
9 |
4 |
3 |
11 |
2 |
2 |
0 |
1 |
6 |
1 |
2 |
45 |
| Drought hazard and annual precipitation predicted to increase in the Sirppujoki river basin, Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
16 |
1 |
4 |
21 |
| Dynamic adaptation of phytoplankton vertical migration to changing grazing and nutrient conditions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Dynamics of a host–parasitoid interaction clarified by modelling and DNA sequencing | 5 |
3 |
5 |
2 |
7 |
8 |
2 |
2 |
3 |
2 |
2 |
2 |
43 |
| Dynamics of cold-water dinoflagellates in the northern Baltic Sea based on 18S rRNA gene metabarcoding | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Early adopters boosting the diffusion of sustainable small-scale energy solutions | 1 |
3 |
6 |
6 |
6 |
4 |
2 |
0 |
1 |
0 |
3 |
3 |
35 |
| Early-successional saproxylic beetles inhabiting a common host-tree type can be sensitive to the spatiotemporal continuity of their substrate | 2 |
3 |
4 |
2 |
3 |
7 |
3 |
0 |
2 |
0 |
3 |
0 |
29 |
| Ecological correlates of riverine diatom and macroinvertebrate alpha and beta diversity across Arctic Fennoscandia | 1 |
3 |
7 |
6 |
2 |
7 |
2 |
2 |
1 |
2 |
1 |
0 |
34 |
| Ecological processes underlying community assembly of aquatic bacteria and macroinvertebrates under contrasting climates on the Tibetan Plateau | 6 |
14 |
8 |
14 |
17 |
13 |
3 |
1 |
3 |
1 |
3 |
4 |
87 |
| Ecological Sufficiency in Climate Policy : Towards Policies for Recomposing Consumption | 26 |
22 |
23 |
16 |
20 |
15 |
1 |
15 |
18 |
12 |
9 |
5 |
182 |
| Ecosystem services at the Archipelago Sea Biosphere Reserve in Finland : a visitor perspective | 4 |
7 |
23 |
10 |
9 |
9 |
8 |
3 |
2 |
3 |
1 |
2 |
81 |
| Ecosystem Services Related to Carbon Cycling - Modeling Present and Future Impacts in Boreal Forests | 18 |
2 |
6 |
1 |
15 |
10 |
1 |
0 |
1 |
5 |
2 |
5 |
66 |
| Ecotoxicity assessment of boreal lake sediments affected by metal mining : Sediment quality triad approach complemented with metal bioavailability and body residue studies | 7 |
0 |
0 |
10 |
9 |
5 |
1 |
1 |
1 |
1 |
0 |
2 |
37 |
| Editorial : Climate impacts on snowpack dynamics | 3 |
4 |
5 |
3 |
7 |
13 |
3 |
3 |
0 |
0 |
2 |
1 |
44 |
| Editorial : Spatio-Temporal Dynamics of Metacommunities - Implications for Conservation and Management | 3 |
2 |
5 |
3 |
6 |
8 |
0 |
0 |
1 |
0 |
0 |
1 |
29 |
| Effect of increased wood harvesting and utilization on required greenhouse gas displacement factors of wood-based products and fuels | 9 |
7 |
22 |
21 |
38 |
11 |
4 |
1 |
4 |
5 |
3 |
2 |
127 |
| Effect of riparian soil moisture on bacterial, fungal and plant communities and microbial decomposition rates in boreal stream-side forests | 4 |
17 |
15 |
5 |
4 |
7 |
5 |
5 |
3 |
2 |
5 |
5 |
77 |
| Effectiveness of biopolymer coagulants in agricultural wastewater treatment at two contrasting levels of pollution | 8 |
5 |
9 |
1 |
3 |
10 |
1 |
0 |
0 |
1 |
0 |
0 |
38 |
| Effectiveness of ecotechnologies in agriculture for the recovery and reuse of carbon and nutrients in the Baltic and boreo-temperate regions : a systematic map | 5 |
5 |
5 |
2 |
2 |
5 |
3 |
0 |
2 |
0 |
0 |
1 |
30 |
| Effects of black carbon mitigation on Arctic climate | 3 |
7 |
13 |
21 |
17 |
11 |
4 |
6 |
19 |
8 |
8 |
3 |
120 |
| Effects of changes in climatic means, variability, and agro-technologies on future wheat and maize yields at 10 sites across the globe | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Effects of climate change and flow regulation on the flow characteristics of a low-relief river within southern boreal climate area | 2 |
3 |
5 |
2 |
2 |
5 |
2 |
0 |
1 |
0 |
3 |
2 |
27 |
| Effects of crop type and production method on arable biodiversity in boreal farmland | 21 |
12 |
11 |
9 |
7 |
12 |
6 |
4 |
2 |
1 |
1 |
1 |
87 |
| Effects of Dispersant on the Petroleum Hydrocarbon Biodegradation and Microbial Communities in Seawater from the Baltic Sea and Norwegian Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
1 |
3 |
| Effects of freeze-drying and use of artificial seawater on phosphorus exchange isotherms in brackish water sediments | 13 |
8 |
9 |
5 |
8 |
7 |
1 |
2 |
0 |
0 |
1 |
0 |
54 |
| Effects of landscape composition on hoverflies (Diptera : Syrphidae) in mass-flowering crop fields within forest-dominated landscapes | 10 |
4 |
8 |
3 |
3 |
3 |
1 |
2 |
1 |
2 |
2 |
0 |
39 |
| Effects of mixed pulp mill sludges on crop yields and quality | 9 |
5 |
8 |
7 |
6 |
18 |
1 |
5 |
6 |
9 |
5 |
3 |
82 |
| Effects of Natura 2000 on nontarget bird and butterfly species based on citizen science data | 59 |
20 |
54 |
19 |
17 |
12 |
18 |
3 |
8 |
2 |
6 |
6 |
224 |
| Effects of paludiculture products on reducing greenhouse gas emissions from agricultural peatlands | 16 |
21 |
17 |
15 |
8 |
9 |
4 |
2 |
6 |
5 |
1 |
1 |
105 |
| Effects of temperature and light exposure on the decay characteristics of fecal indicators, norovirus, and Legionella in mesocosms simulating subarctic river water | 20 |
16 |
26 |
10 |
17 |
13 |
4 |
0 |
2 |
3 |
4 |
3 |
118 |
| Effects of Top Predator Re-Establishment and Fishing on a Simulated Food Web: Allometric Trophic Network Model for Lake Oulujärvi | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Efficient protection of the Baltic Sea needs a revision of phosphorus metric | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
1 |
2 |
| EKLIPSE : engaging knowledge holders and networks for evidence-informed European policy on biodiversity and ecosystem services | 3 |
3 |
8 |
4 |
4 |
9 |
2 |
122 |
1 |
3 |
2 |
2 |
163 |
| Ekologinen kompensaatio Suomessa: analyysi sääntelyn vahvuuksista, heikkouksista ja kehitysmahdollisuuksista | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Elements of metacommunity structure of diatoms and macroinvertebrates within stream networks differing in environmental heterogeneity | 10 |
12 |
12 |
2 |
5 |
13 |
2 |
5 |
3 |
6 |
6 |
4 |
80 |
| Embodied emissions of buildings : A forgotten factor in green building certificates | 13 |
12 |
11 |
13 |
12 |
9 |
3 |
3 |
5 |
7 |
3 |
0 |
91 |
| Embodied public experiments on sustainable eating : demonstrating alternative proteins in Finnish schools | 7 |
1 |
7 |
3 |
4 |
5 |
0 |
1 |
0 |
0 |
0 |
1 |
29 |
| Emergent rural–urban relations in Covid‐19 disturbances: Multi‐locality affecting sustainability of rural change | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
1 |
2 |
| Emission reduction potential of different types of Finnish buildings through energy retrofits | 3 |
4 |
10 |
7 |
8 |
12 |
4 |
307 |
43 |
2 |
1 |
4 |
405 |
| Emissions and power demand in optimal energy retrofit scenarios of the Finnish building stock by 2050 | 1 |
12 |
18 |
10 |
14 |
9 |
1 |
0 |
0 |
3 |
3 |
2 |
73 |
| Empirical insights into knowledge-weaving processes in strategic environmental research | 0 |
21 |
8 |
13 |
9 |
8 |
3 |
3 |
1 |
3 |
2 |
3 |
74 |
| Energetic voices on social media? : Strategic Niche Management and Finnish Facebook debate on biogas and heat pumps | 5 |
3 |
9 |
5 |
10 |
10 |
3 |
2 |
2 |
2 |
1 |
0 |
52 |
| Energy transition looming behind the headlines? : Newspaper coverage of biogas production in Finland | 5 |
2 |
5 |
4 |
3 |
2 |
1 |
0 |
0 |
0 |
0 |
2 |
24 |
| Enhanced threat of tick-borne infections within cities? Assessing public health risks due to ticks in urban green spaces in Helsinki, Finland | 3 |
5 |
5 |
3 |
5 |
9 |
1 |
0 |
2 |
0 |
0 |
1 |
34 |
| Ennallistaminen oikeudellisena velvoitteena - luontokadon hillinnän valloittamaton rintama Suomen ympäristöoikeudessa | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Entisten turvetuotantoalueiden luontoarvojen palauttaminen ja ilmastonmuutoksen hillintä | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Environmental determinants of lake macrophyte communities in Baikal Siberia | 3 |
2 |
7 |
2 |
3 |
5 |
1 |
0 |
0 |
0 |
0 |
0 |
23 |
| Environmental factors are primary determinants of different facets of pond macroinvertebrate alpha and beta diversity in a human-modified landscape | 9 |
4 |
5 |
5 |
7 |
8 |
4 |
2 |
1 |
1 |
2 |
2 |
50 |
| Environmental journalism in the Nordic countries | 14 |
21 |
24 |
13 |
16 |
16 |
4 |
4 |
3 |
5 |
1 |
0 |
121 |
| Environmental Risk Assessment of Wetland Ecosystems Using Bayesian Belief Networks | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
1 |
2 |
| Environmental sustainability assessment of a polyester T-shirt – Comparison of circularity strategies | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
7 |
2 |
6 |
17 |
| Environmental variables driving species and genus level changes in annual plankton biomass | 4 |
13 |
4 |
7 |
16 |
16 |
4 |
3 |
2 |
1 |
2 |
4 |
76 |
| Errors related to the automatized satellite-based change detection of boreal forests in Finland | 4 |
4 |
5 |
6 |
7 |
3 |
0 |
1 |
1 |
1 |
2 |
1 |
35 |
| Establishing fluvial silicon regimes and their stability across the Northern Hemisphere | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Estimating cation exchange capacity from agronomic soil tests : Comparing Mehlich‐3 and ammonium acetate sum of cations | 0 |
19 |
15 |
9 |
8 |
8 |
3 |
2 |
3 |
1 |
3 |
3 |
74 |
| Estimating cation exchange capacity from agronomic soil tests: comparing Mehlich-3 and ammonium acetate sum of cations | 10 |
18 |
13 |
12 |
11 |
8 |
2 |
3 |
4 |
2 |
3 |
3 |
89 |
| Estimating impact likelihoods from probabilistic projections of climate and socio-economic change using impact response surfaces | 11 |
11 |
11 |
6 |
11 |
5 |
6 |
4 |
2 |
1 |
3 |
3 |
74 |
| Estimating nutrient thresholds for eutrophication management : Novel insights from understudied lake types | 2 |
5 |
15 |
10 |
6 |
13 |
1 |
5 |
1 |
1 |
2 |
2 |
63 |
| Estimating salinity stress via hsp70 expression in the invasive round goby (Neogobius melanostomus) : implications for further range expansion | 3 |
3 |
5 |
7 |
2 |
5 |
0 |
2 |
0 |
0 |
1 |
0 |
28 |
| Estimating the economic value of hydropeaking externalities in regulated rivers | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| EU wood production vs. biodiversity goals – possible reconciliation in Finland? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
4 |
2 |
5 |
14 |
| Europe-wide spatial trends in copper and imidacloprid sensitivity of macroinvertebrate assemblages | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| European forest sinks and climate targets: past trends, main drivers, and future forecasts | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
1 |
| European Union legislation on macroalgae products | 3 |
5 |
12 |
11 |
10 |
3 |
2 |
2 |
1 |
1 |
1 |
1 |
52 |
| Eutrophication causes invertebrate biodiversity loss and decreases cross-taxon congruence across anthropogenically-disturbed lakes | 4 |
8 |
16 |
2 |
6 |
10 |
3 |
1 |
2 |
5 |
8 |
2 |
67 |
| Eutrophication reduces the nutritional value of phytoplankton in boreal lakes | 6 |
6 |
7 |
2 |
8 |
6 |
1 |
3 |
3 |
5 |
5 |
7 |
59 |
| Evaluating complex relationships between ecological indicators and environmental factors in the Baltic Sea : A machine learning approach | 10 |
2 |
8 |
5 |
8 |
9 |
1 |
5 |
3 |
3 |
3 |
1 |
58 |
| Evaluating multiannual sedimentary nutrient retention in agricultural two-stage channels | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Evaluating policy coherence and integration for adaptation: the case of EU policies and Arctic cross-border climate change impacts | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Evaluation and validation of detailed and simplified models of the uncertainty of unified pHabsH2O measurements in aqueous solutions | 11 |
11 |
10 |
4 |
11 |
10 |
6 |
3 |
3 |
5 |
2 |
2 |
78 |
| Evaluation of historic and operational satellite radar altimetry missions for constructing consistent long-term lake water level records | 3 |
6 |
17 |
9 |
12 |
13 |
4 |
4 |
2 |
1 |
2 |
2 |
75 |
| Evaluation of sustainable development strategies and policies : The need for more timely indicators | 4 |
1 |
2 |
1 |
5 |
2 |
1 |
1 |
1 |
1 |
0 |
0 |
19 |
| Evaluation of X-ray fluorescence for analysing critical elements in three electronic waste matrices: A comprehensive comparison of analytical techniques | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Evidence for bottom‐up effects of moth abundance on forest birds in the north‐boreal zone alone | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Evidence of environmental threat caused by sea-dumped chemical warfare agents: Exposure status of hagfish in the skagerrak strait | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Exceptions and exemptions under the ballast water management convention – Sustainable alternatives for ballast water management? | 11 |
4 |
21 |
19 |
13 |
16 |
1 |
2 |
0 |
1 |
1 |
0 |
89 |
| Expansion of the built-up areas in Finnish city regions : The approach of travel-related urban zones | 13 |
9 |
11 |
19 |
16 |
17 |
3 |
1 |
1 |
2 |
2 |
6 |
100 |
| Exploring operational ecosystem service definitions : the case of boreal forests | 10 |
9 |
12 |
24 |
18 |
16 |
3 |
9 |
13 |
5 |
6 |
6 |
131 |
| Exploring the impacts of microplastics and associated chemicals in the terrestrial environment – Exposure of soil invertebrates to tire particles | 5 |
6 |
7 |
7 |
17 |
14 |
3 |
2 |
1 |
5 |
0 |
1 |
68 |
| Exploring the potential of circular economy to mitigate pressures on biodiversity | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
7 |
6 |
4 |
21 |
| Exploring the re-emergence of industrial policy : Perceptions regarding low-carbon energy transitions in Germany, the United Kingdom and Denmark | 4 |
7 |
10 |
15 |
4 |
13 |
2 |
2 |
1 |
3 |
2 |
3 |
66 |
| Exposure to dissolved TNT causes multilevel biological effects in Baltic mussels (Mytilus spp.) | 5 |
5 |
11 |
6 |
4 |
9 |
0 |
1 |
2 |
0 |
0 |
2 |
45 |
| Extending the shared socioeconomic pathways for adaptation planning of blue tourism | 10 |
13 |
8 |
7 |
10 |
9 |
5 |
4 |
6 |
2 |
5 |
1 |
80 |
| Extensive Coverage of Marine Mineral Concretions Revealed in Shallow Shelf Sea Areas | 7 |
4 |
12 |
2 |
7 |
9 |
2 |
0 |
2 |
2 |
5 |
2 |
54 |
| Extracellular enzyme activity in the coastal upwelling system off Peru: a mesocosm experiment | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
4 |
3 |
3 |
13 |
| Facilitating practices for sustainable car sharing policies : An integrated approach utilizing user data, urban form variables and mobility patterns | 9 |
3 |
11 |
7 |
13 |
13 |
11 |
4 |
1 |
10 |
13 |
12 |
107 |
| Factors contributing to the relevance and continuity of life cycle assessment networks | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
3 |
2 |
5 |
11 |
| Factors regulating the coastal nutrient filter in the Baltic Sea | 4 |
5 |
11 |
11 |
21 |
18 |
18 |
27 |
14 |
19 |
7 |
4 |
159 |
| Farm characteristics shape farmers’ cover crop choices in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Farmers’ experiences of how under-sown clovers, ryegrasses, and timothy perform in northern European crop production systems | 5 |
3 |
11 |
5 |
6 |
8 |
0 |
1 |
5 |
3 |
5 |
0 |
52 |
| Female-biased sex ratios and delayed puberty in two fish species with different Ecologies in an Anthropogenically affected urban lake | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Field testing a pilot-scale system for alkaline dehydration of source-separated human urine : a case study in Finland | 12 |
5 |
11 |
6 |
6 |
9 |
2 |
5 |
1 |
0 |
1 |
0 |
58 |
| Filling in socio‐ecological knowledge gaps to support marine spatial planning in data‐scarce areas: Example from Zanzibar | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Finding the essential : improving conservation monitoring across scales | 2 |
5 |
6 |
6 |
6 |
8 |
1 |
1 |
0 |
0 |
0 |
1 |
36 |
| Fine particle emissions from sauna stoves : effects of combustion appliance and fuel, and implications for the Finnish emission inventory | 7 |
14 |
11 |
4 |
8 |
11 |
1 |
4 |
3 |
4 |
4 |
2 |
73 |
| Fine-grained climate velocities reveal vulnerability of protected areas to climate change | 5 |
1 |
9 |
3 |
7 |
9 |
2 |
1 |
2 |
4 |
3 |
1 |
47 |
| Finnish botanists in the mires of Olonets region in Russian Karelia during the Second World War | 3 |
2 |
4 |
3 |
6 |
2 |
1 |
2 |
1 |
0 |
2 |
1 |
27 |
| Finnish dairy farmers’ perceptions of justice in the transition to carbon-neutral farming | 6 |
3 |
6 |
6 |
3 |
5 |
2 |
1 |
1 |
0 |
2 |
1 |
36 |
| Finnish energy renovation subsidies in multifamily apartment buildings: Lessons learnt and best practices | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Finnish inventory data of underwater marine biodiversity | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| First application of IFCB high-frequency imaging-in-flow cytometry to investigate bloom-forming filamentous cyanobacteria in the Baltic Sea | 12 |
7 |
9 |
9 |
8 |
15 |
5 |
10 |
5 |
1 |
6 |
1 |
88 |
| Flies are important pollinators of mass-flowering caraway and respond to landscape and floral factors differently from honeybees | 14 |
9 |
8 |
6 |
5 |
16 |
6 |
8 |
6 |
2 |
0 |
6 |
86 |
| Flow regime alteration in Arctic rivers due to dam operations and climate change | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Food web assessments in the Baltic Sea : Models bridging the gap between indicators and policy needs | 1 |
7 |
11 |
5 |
6 |
13 |
3 |
5 |
3 |
1 |
1 |
2 |
58 |
| Forest carbon payments: A multidisciplinary review of policy options for promoting carbon storage in EU member states | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Forest conservation as a CO2 offset measure: a case of an urban development project in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Forest data governance as a reflection of forest governance : Institutional change and endurance in Finland and Canada | 10 |
10 |
20 |
3 |
14 |
16 |
7 |
9 |
4 |
2 |
3 |
3 |
101 |
| Forest policy in Nordic countries: Expert opinions on future needs, uncertainties, and recommendations | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Forest restoration benefits common and rare wood-decomposing fungi with a delay | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Formal commitments versus actual practices? Narratives as tools of epistemic governance in the debate over Finnish forestry | 0 |
0 |
21 |
16 |
15 |
13 |
5 |
0 |
3 |
2 |
5 |
1 |
81 |
| Four new epiphytic species in the Micarea prasina group from Europe | 13 |
10 |
18 |
6 |
16 |
14 |
11 |
2 |
4 |
2 |
5 |
6 |
107 |
| Framework to study the effects of climate change on vulnerability of ecosystems and societies : case study of nitrates in drinking water in Southern Finland | 4 |
4 |
6 |
4 |
3 |
12 |
3 |
0 |
6 |
12 |
8 |
2 |
64 |
| Framing climate futures: the media representations of climate and energy policies in Finnish broadcasting company news | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
4 |
8 |
| Framing just transition: The case of sustainable food system transition in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Framing the peat - the political ecology of Finnish mire policies and law | 3 |
6 |
15 |
8 |
6 |
8 |
1 |
0 |
1 |
0 |
1 |
0 |
49 |
| From global Doughnut sustainability to local tourism destination management | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| From isolated labels and nudges to sustained tinkering : assessing long-term changes in sustainable eating at a lunch restaurant | 2 |
27 |
48 |
5 |
7 |
12 |
2 |
2 |
0 |
0 |
0 |
1 |
106 |
| From meta-system theory to the sustainable management of rivers in the Anthropocene | 5 |
6 |
13 |
8 |
7 |
8 |
3 |
6 |
2 |
2 |
2 |
1 |
63 |
| From timber to carbon: Stakeholder acceptance of policy measures supporting forest management transition in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| From Top–Down Regulation to Bottom–Up Solutions : Reconfiguring Governance of Agricultural Nutrient Loading to Waters | 5 |
2 |
4 |
3 |
16 |
8 |
1 |
2 |
0 |
0 |
1 |
2 |
44 |
| Functional diversity and trait composition of vascular plant and Sphagnum moss communities during peatland succession across land uplift regions | 2 |
4 |
10 |
5 |
6 |
4 |
0 |
1 |
4 |
2 |
3 |
0 |
41 |
| Fungal assemblages in predictive stream bioassessment : A cross-taxon comparison along multiple stressor gradients | 7 |
2 |
2 |
8 |
5 |
4 |
3 |
1 |
4 |
1 |
1 |
0 |
38 |
| Fungi originating from tree leaves contribute to fungal diversity of litter in streams | 3 |
1 |
8 |
5 |
3 |
6 |
3 |
2 |
2 |
1 |
0 |
3 |
37 |
| Future area expansion outweighs increasing drought risk for soybean in Europe | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
81 |
0 |
5 |
87 |
| Future temperature and salinity do not exert selection pressure on cyst germination of a toxic phytoplankton species | 3 |
4 |
8 |
5 |
10 |
7 |
3 |
7 |
1 |
1 |
1 |
1 |
51 |
| Futures images of woodchips as an energy source in Finland | 5 |
3 |
7 |
6 |
6 |
6 |
1 |
1 |
0 |
0 |
0 |
0 |
35 |
| Generalist Life Cycle Aids Persistence of Alexandrium ostenfeldii (Dinophyceae) in Seasonal Coastal Habitats of the Baltic Sea(1) | 7 |
1 |
6 |
12 |
12 |
17 |
9 |
12 |
1 |
2 |
1 |
2 |
82 |
| Geodiversity data for Europe | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Geopolymers as active capping materials for in situ remediation of metal (loid)-contaminated lake sediments | 10 |
5 |
11 |
4 |
8 |
8 |
1 |
0 |
0 |
0 |
0 |
0 |
47 |
| Geospatial Artificial Intelligence (GeoAI) in the Integrated Hydrological and Fluvial Systems Modeling : Review of Current Applications and Trends | 22 |
6 |
18 |
14 |
12 |
20 |
3 |
2 |
8 |
3 |
4 |
1 |
113 |
| GIS and land cover-based assessment of ecosystem services in the North Karelia Biosphere Reserve, Finland | 10 |
4 |
5 |
3 |
3 |
7 |
4 |
3 |
2 |
1 |
0 |
0 |
42 |
| GIS-based planning of buffer zones for protection of boreal streams and their riparian forests | 11 |
24 |
26 |
17 |
28 |
14 |
7 |
2 |
2 |
8 |
1 |
1 |
141 |
| Global climate change and the Baltic Sea ecosystem : direct and indirect effects on species, communities and ecosystem functioning | 16 |
3 |
9 |
7 |
4 |
12 |
1 |
2 |
3 |
0 |
1 |
2 |
60 |
| Global data set of long-term summertime vertical temperature profiles in 153 lakes | 7 |
4 |
8 |
6 |
4 |
9 |
1 |
1 |
1 |
0 |
0 |
0 |
41 |
| Global patterns and drivers of ecosystem functioning in rivers and riparian zones | 0 |
2 |
5 |
2 |
9 |
6 |
0 |
1 |
3 |
3 |
2 |
4 |
37 |
| Global Resources Outlook 2024: Bend the trend - Pathways to a liveable planet as resource use spikes | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Globally widespread and increasing violations of environmental flow envelopes | 2 |
8 |
9 |
1 |
16 |
8 |
1 |
2 |
3 |
0 |
2 |
0 |
52 |
| Going carless in different urban fabrics: socio-demographics of household car ownership | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
29 |
2 |
0 |
1 |
32 |
| Good eutrophication status is a challenging goal for coastal waters | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Governance and Practices for Achieving Sustainable and Resilient Urban Water Services | 7 |
3 |
20 |
6 |
12 |
11 |
14 |
8 |
6 |
17 |
7 |
5 |
116 |
| Governance innovations for forest ecosystem service provision : Insights from an EU-wide survey | 7 |
8 |
10 |
9 |
9 |
7 |
1 |
0 |
0 |
1 |
0 |
0 |
52 |
| Governing complexity : Integrating science, governance, and law to manage accelerating change in the globalized commons | 12 |
4 |
11 |
15 |
16 |
14 |
10 |
12 |
3 |
3 |
2 |
5 |
107 |
| Governing the provision of insurance value from ecosystems | 3 |
2 |
7 |
4 |
10 |
11 |
0 |
0 |
1 |
0 |
0 |
1 |
39 |
| Gradients of anthropogenic nutrient enrichment alter N Composition and DOM stoichiometry in freshwater ecosystems | 3 |
7 |
7 |
5 |
3 |
7 |
2 |
0 |
2 |
3 |
1 |
2 |
42 |
| Graph embedding with data uncertainty | 4 |
1 |
7 |
5 |
6 |
10 |
5 |
2 |
0 |
0 |
3 |
1 |
44 |
| Graph-embedded subspace support vector data description | 8 |
4 |
9 |
11 |
11 |
12 |
1 |
1 |
4 |
0 |
1 |
2 |
64 |
| Gypsum amendment of agricultural fields to decrease phosphorus losses – Evidence on a catchment scale | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Gypsum amendment of arable fields as a water protection measure – farmers’ experience, phosphorus reduction potential and associated costs drawn from a large scale pilot | 4 |
10 |
7 |
3 |
8 |
10 |
3 |
4 |
13 |
7 |
7 |
6 |
82 |
| Gypsum and structure lime amendments in boreal agricultural clay soils: Do climate emissions compromise water quality benefits? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Habitat amount and distribution modify community dynamics under climate change | 1 |
5 |
7 |
7 |
3 |
7 |
3 |
2 |
1 |
1 |
1 |
0 |
38 |
| Habitat associations of red-listed epiphytic lichens in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
2 |
3 |
8 |
| Habitat loss and deterioration explain the disappearance of populations of threatened vascular plants, bryophytes and lichens in a hemiboreal landscape | 5 |
6 |
2 |
7 |
5 |
4 |
0 |
0 |
0 |
0 |
0 |
3 |
32 |
| Habitat patchiness, ecological connectivity and the uneven recovery of boreal stream ecosystems from an experimental drought | 2 |
3 |
9 |
3 |
7 |
14 |
1 |
1 |
0 |
0 |
0 |
0 |
40 |
| Habituation or sensitization? Short-term adjustment of flight initiation distance in incubating common eiders | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Haja-asutusalueen jätevesihuolloin hallintokäytäneet Suomessa, Ruotsissa ja Norjassa | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Half-century trends in alpha and beta diversity of phytoplankton summer communities in the Helsinki Archipelago, the Baltic Sea | 0 |
0 |
25 |
9 |
18 |
13 |
1 |
4 |
4 |
4 |
4 |
0 |
82 |
| Harmful algal blooms and their effects in coastal seas of Northern Europe | 8 |
4 |
22 |
6 |
10 |
8 |
16 |
12 |
4 |
0 |
0 |
5 |
95 |
| Hazardous substances in the sediments and their pathways from potential sources in the eastern Gulf of Finland | 0 |
0 |
0 |
0 |
0 |
6 |
1 |
2 |
1 |
2 |
1 |
0 |
13 |
| Head-mounted display-based augmented reality for water quality visualisation | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Health impacts of changes in travel patterns in Greater Accra Metropolitan Area, Ghana | 10 |
12 |
7 |
7 |
13 |
12 |
9 |
6 |
2 |
13 |
6 |
0 |
97 |
| Heavy metals from heavy land use? Spatio-temporal patterns of urban runoff metal loads | 4 |
8 |
14 |
4 |
9 |
6 |
3 |
5 |
5 |
0 |
2 |
1 |
61 |
| Helsinki by nature : The Nature Step to Respiratory Health | 0 |
2 |
6 |
23 |
12 |
7 |
3 |
3 |
1 |
1 |
0 |
2 |
60 |
| High focus on threatened species and habitats may undermine biodiversity conservation: Evidence from the northern Baltic Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
5 |
3 |
1 |
1 |
10 |
| High organic carbon content constricts the potential for stable organic carbon accrual in mineral agricultural soils in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| High-latitude EU Habitats Directive species at risk due to climate change and land use | 8 |
7 |
15 |
5 |
13 |
15 |
7 |
2 |
0 |
2 |
1 |
3 |
78 |
| Higher thermal plasticity in flowering phenology increases flowering output | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Historical and current occurrence of microplastics in water and sediment of a Finnish lake affected by WWTP effluents | 17 |
18 |
12 |
10 |
14 |
11 |
6 |
2 |
6 |
6 |
10 |
7 |
119 |
| Historical Biogeography of Sub‐Saharan African Spleenworts | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Historical contingency via priority effects counteracts environmental change on metacommunity dynamics across decades | 3 |
2 |
3 |
5 |
7 |
16 |
0 |
0 |
0 |
0 |
1 |
0 |
37 |
| Hospitals and households as primary emission sources for risk-posing pharmaceuticals in municipal wastewater | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
14 |
0 |
1 |
15 |
| House and socio-demographic features vs. electricity consumption time series in main heating mode classification | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| How copepods can eat toxins without getting sick - gut bacteria help zooplankton to feed in cyanobacteria blooms | 3 |
2 |
7 |
7 |
9 |
13 |
1 |
3 |
0 |
1 |
3 |
0 |
49 |
| How do rural second homes affect human health and well-being? : Review of potential impacts | 5 |
1 |
4 |
2 |
3 |
6 |
0 |
0 |
1 |
3 |
0 |
0 |
25 |
| How does action competence explain young people’s sustainability action? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| How does the circular economy discourse affect policy-making? The case of streamlining waste utilisation in Finnish earthworks | 2 |
4 |
7 |
28 |
24 |
4 |
2 |
2 |
0 |
0 |
1 |
0 |
74 |
| How effective are river basin management plans in reaching the nutrient load reduction targets? | 3 |
1 |
8 |
1 |
1 |
13 |
3 |
1 |
2 |
1 |
1 |
2 |
37 |
| How farmers approach soil carbon sequestration? : Lessons learned from 105 carbon-farming plans | 8 |
17 |
18 |
13 |
8 |
13 |
8 |
3 |
6 |
5 |
5 |
1 |
105 |
| How have measuring, mapping and valuation enhanced governance of ecosystem services? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| How threats inform conservation planning : A systematic review protocol | 4 |
4 |
5 |
2 |
12 |
6 |
5 |
3 |
8 |
3 |
4 |
2 |
58 |
| How to measure the social sustainability of the circular economy? Developing and piloting social circular economy indicators in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
7 |
4 |
2 |
2 |
15 |
| How to model algal blooms in any lake on earth | 6 |
6 |
15 |
4 |
12 |
7 |
2 |
8 |
4 |
2 |
2 |
7 |
75 |
| How to reach a safe circular economy? - Perspectives on reconciling the waste, product and chemicals regulation | 2 |
1 |
5 |
7 |
7 |
7 |
1 |
1 |
0 |
0 |
4 |
9 |
44 |
| How unnecessarily high abatement costs and unresolved distributional issues undermine nutrient reductions to the Baltic Sea | 2 |
4 |
6 |
2 |
2 |
6 |
1 |
0 |
0 |
0 |
0 |
2 |
25 |
| Human actions were responsible for both initiation and termination of varve preservation in Lake Vesijärvi, southern Finland | 5 |
2 |
5 |
4 |
4 |
2 |
2 |
4 |
1 |
13 |
8 |
4 |
54 |
| Human health in systemic adaptation to climate change : insights from flood risk management in a river basin | 4 |
7 |
7 |
10 |
12 |
8 |
2 |
2 |
2 |
0 |
2 |
0 |
56 |
| Human-induced loss of functional and phylogenetic diversity is mediated by concomitant deterministic processes in subtropical aquatic insect communities | 5 |
8 |
11 |
10 |
6 |
12 |
1 |
2 |
0 |
0 |
1 |
2 |
58 |
| Hydraulic and physical properties of managed and intact peatlands : application of the van Genuchten-Mualem models to peat soils | 5 |
4 |
7 |
7 |
9 |
6 |
3 |
5 |
10 |
4 |
7 |
4 |
71 |
| Hydrography-driven variability of optically active constituents of water in the South Brazilian Bight : Biogeochemical implications | 3 |
4 |
4 |
3 |
2 |
4 |
0 |
0 |
0 |
0 |
0 |
0 |
20 |
| Hydrological Forecasting and Real Time Monitoring in Finland : The Watershed Simulation and Forecasting System (WSFS) | 8 |
10 |
24 |
8 |
29 |
9 |
2 |
1 |
0 |
21 |
16 |
9 |
137 |
| Hydrometeorological drought analysis through Two-variate Standardized Index for the Paraná River Basin, Brazil | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Hydropowering sustainability transformation: policy frames on river use and restoration in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
2 |
4 |
2 |
12 |
| Identifying areas prone to coastal hypoxia - the role of topography | 1 |
2 |
6 |
5 |
14 |
9 |
1 |
1 |
3 |
1 |
5 |
2 |
50 |
| Identifying biotic drivers of population dynamics in a benthic–pelagic community | 5 |
1 |
6 |
2 |
5 |
8 |
0 |
1 |
0 |
0 |
0 |
2 |
30 |
| Identifying multiple stressors that influence eutrophication in a Finnish agricultural river | 8 |
9 |
9 |
2 |
5 |
12 |
3 |
1 |
2 |
0 |
0 |
2 |
53 |
| Identifying Policy Actions Supporting Weather-Related Risk Management and Climate Change Adaptation in Finland | 7 |
4 |
6 |
5 |
5 |
10 |
1 |
1 |
4 |
0 |
2 |
2 |
47 |
| Identity of the subalpine–subarctic corticioid fungus Megalocystidium leucoxanthum (Russulales, Basidiomycota) and six related species | 8 |
5 |
12 |
3 |
12 |
8 |
0 |
0 |
1 |
0 |
1 |
0 |
50 |
| Ilmastovalinta lounasruokailussa | 9 |
7 |
3 |
4 |
6 |
5 |
0 |
2 |
1 |
0 |
1 |
1 |
39 |
| Immunological resilience and biodiversity for prevention of allergic diseases and asthma | 8 |
7 |
8 |
7 |
8 |
8 |
2 |
3 |
0 |
2 |
0 |
2 |
55 |
| Impact of a climate network : The role of intermediaries in local level climate action | 23 |
14 |
12 |
19 |
8 |
10 |
6 |
3 |
3 |
2 |
2 |
2 |
104 |
| Impact of home market on business development and internationalization of demand response firms | 7 |
8 |
7 |
2 |
7 |
11 |
0 |
1 |
1 |
0 |
1 |
1 |
46 |
| Impact of home market on business development and internationalization of demand response firms | 5 |
10 |
9 |
7 |
8 |
9 |
2 |
2 |
1 |
0 |
0 |
0 |
53 |
| Impact of structural changes in wood-using industries on net carbon emissions in Finland | 22 |
18 |
51 |
37 |
53 |
26 |
14 |
15 |
25 |
27 |
10 |
16 |
314 |
| Impacts of hydro-climatically varying years on ice growth and decay in a subarctic river | 2 |
1 |
1 |
2 |
3 |
0 |
2 |
0 |
0 |
0 |
0 |
1 |
12 |
| Impacts of reduced inorganic N:P ratio on three distinct plankton communities in the Humboldt upwelling system | 2 |
1 |
9 |
4 |
5 |
7 |
2 |
2 |
3 |
1 |
3 |
4 |
43 |
| Impacts of the IUCN Red List of Ecosystems on conservation policy and practice | 3 |
10 |
10 |
5 |
8 |
15 |
5 |
1 |
1 |
0 |
1 |
4 |
63 |
| Implications on crustal structure from the South Finland Coastal (SOFIC) deep seismic sounding profile | 0 |
0 |
0 |
15 |
45 |
33 |
2 |
2 |
1 |
1 |
1 |
2 |
102 |
| Improved environmental status : 50 years of declining fish mercury levels in boreal and subarctic Fennoscandia | 5 |
8 |
16 |
14 |
12 |
17 |
25 |
80 |
3 |
1 |
2 |
3 |
186 |
| Improving data quality, applicability and transparency of national water accounts - A case study for Finland | 9 |
7 |
19 |
10 |
10 |
18 |
4 |
1 |
4 |
1 |
2 |
2 |
87 |
| Improving impact assessments to reduce impacts of deep-sea fisheries on vulnerable marine ecosystems | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Improving resilience of reservoir operation in the context of watercourse regulation in Finland | 4 |
8 |
11 |
4 |
10 |
4 |
0 |
0 |
0 |
0 |
0 |
0 |
41 |
| Improving sustainability teaching by grouping and interrelating pedagogical approaches and sustainability competences : Evidence from 15 Worldwide Higher Education Institutions | 0 |
0 |
25 |
13 |
21 |
11 |
4 |
3 |
1 |
5 |
6 |
3 |
92 |
| Improving the representation of adaptation in climate change impact models | 2 |
6 |
6 |
4 |
3 |
7 |
1 |
1 |
0 |
0 |
0 |
0 |
30 |
| In situ remediation of metal(loid)-contaminated lake sediments with alkali-activated blast furnace slag granule amendment : A field experiment | 6 |
5 |
8 |
10 |
12 |
9 |
3 |
0 |
0 |
1 |
0 |
2 |
56 |
| In-depth characterization of denitrifier communities across different soil ecosystems in the tundra | 3 |
5 |
11 |
9 |
11 |
16 |
1 |
5 |
3 |
0 |
1 |
1 |
66 |
| Inconsistencies in the EU regulatory risk assessment of PFAS call for readjustment | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Incorporating landscape heterogeneity into multi-objective spatial planning improves biodiversity conservation of semi-natural grasslands | 0 |
1 |
5 |
2 |
5 |
9 |
0 |
1 |
1 |
0 |
2 |
0 |
26 |
| Incorporation of plastic debris into the nests of great cormorants (Phalacrocorax carbo sinensis) in the Gulf of Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Increase in gross primary production of boreal forests balanced out by increase in ecosystem respiration | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Increased nutrient retention and cyanobacterial blooms in a future coastal zone | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Increases in organic carbon and nitrogen concentrations in boreal forested catchments — Changes driven by climate and deposition | 7 |
2 |
6 |
4 |
7 |
6 |
2 |
0 |
0 |
0 |
1 |
1 |
36 |
| Increasing loss of mature boreal forests around protected areas with red-listed forest species | 5 |
3 |
5 |
5 |
4 |
1 |
0 |
2 |
0 |
0 |
0 |
0 |
25 |
| Increasing the circularity of packaging along pharmaceuticals value chain | 10 |
5 |
9 |
8 |
6 |
10 |
3 |
13 |
15 |
16 |
12 |
7 |
114 |
| Industrial workers’ perceptions on just transition and work in four Finnish regions: Three-level solutions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Influence of coagulant type on nutrient uptake of plants and the nutrient and micropollutants leaching from anaerobically digested sludge amended soils | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Influence of Environmental Variables on Biochemical Biomarkers in the Amphipod Monoporeia affinis from the Gulf of Riga (Baltic Sea) | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
13 |
21 |
1 |
2 |
37 |
| Influence of season-depending ecological variables on biomarker baseline levels in mussels (Mytilus trossulus) from two Baltic Sea subregions | 3 |
3 |
8 |
2 |
7 |
5 |
0 |
1 |
3 |
0 |
2 |
2 |
36 |
| Influence of spatial resolution on population PM2.5 exposure and health impacts | 12 |
4 |
11 |
16 |
20 |
13 |
2 |
0 |
1 |
0 |
1 |
1 |
81 |
| Influence of vegetation maintenance on flow and mixing: case study comparing full cut with high-coverage conditions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
17 |
62 |
0 |
1 |
80 |
| Influence of water color and catchment lake cover on stream macroinvertebrate communities: Ecological insights into browning effects | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Inheritance of Material Wealth in a Natural Population | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Institutions for governing biodiversity offsetting : An analysis of rights and responsibilities | 3 |
5 |
8 |
2 |
10 |
9 |
3 |
3 |
0 |
2 |
0 |
2 |
47 |
| Insurance Value of Ecosystems : An Introduction | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Integrated frameworks for assessing and managing health risks in the context of managed aquifer recharge with river water | 7 |
2 |
7 |
5 |
7 |
11 |
1 |
2 |
0 |
1 |
0 |
1 |
44 |
| Integrating climate change into legislative drafting: An analysis of regulatory impact assessment obligations and practices in the EU and Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Integrating diverse model results into decision support for good environmental status and blue growth | 4 |
5 |
12 |
9 |
13 |
9 |
5 |
2 |
3 |
3 |
6 |
1 |
72 |
| Integrating experimental and distribution data to predict future species patterns | 13 |
19 |
13 |
5 |
8 |
4 |
0 |
4 |
0 |
2 |
2 |
2 |
72 |
| Integrating green infrastructure and ecosystem services in land use planning : Results from two Finnish case studies | 38 |
35 |
29 |
15 |
34 |
12 |
1 |
3 |
11 |
2 |
2 |
3 |
185 |
| Integrating pigment and fatty acid profiles for enhanced estimation of seston community composition | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| INTEL-TAU : A Color Constancy Dataset | 3 |
4 |
11 |
25 |
11 |
9 |
1 |
4 |
2 |
6 |
10 |
11 |
97 |
| Interaction between the land and the sea : sources and patterns of nutrients in the scattered coastal zone of a eutrophied sea | 5 |
5 |
7 |
8 |
7 |
6 |
1 |
0 |
1 |
0 |
0 |
1 |
41 |
| Interannual and seasonal variability of the air–sea CO2 exchange at Utö in the coastal region of the Baltic Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Intercomparison study on commonly used methods to determine microplastics in wastewater and sludge samples | 6 |
5 |
9 |
7 |
7 |
8 |
1 |
2 |
2 |
1 |
1 |
0 |
49 |
| Intermediaries in accelerating transitions : Introduction to the special issue | 24 |
17 |
18 |
11 |
25 |
17 |
18 |
9 |
3 |
5 |
2 |
1 |
150 |
| Intermediating policy for transitions towards net-zero energy buildings | 4 |
4 |
8 |
4 |
10 |
10 |
0 |
0 |
1 |
2 |
0 |
0 |
43 |
| Interoperable vocabulary for marine microbial flow cytometry | 0 |
0 |
0 |
0 |
66 |
9 |
4 |
5 |
5 |
5 |
5 |
0 |
99 |
| Interplay between low-carbon energy transitions and national security : An analysis of policy integration and coherence in Estonia, Finland and Scotland | 6 |
6 |
16 |
7 |
11 |
20 |
3 |
0 |
2 |
4 |
0 |
0 |
75 |
| Interplay between skin microbiota and immunity in atopic individuals | 3 |
1 |
2 |
4 |
3 |
2 |
0 |
0 |
1 |
0 |
0 |
0 |
16 |
| Interplay of policy experimentation and institutional change in sustainability transitions : The case of mobility as a service in Finland | 10 |
7 |
6 |
7 |
9 |
11 |
1 |
0 |
1 |
0 |
0 |
0 |
52 |
| Interrelations between security and the zero‑carbon energy transition in the Finnish and Norwegian Arctic | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Introduction to GlobSnow Snow Extent products with considerations for accuracy assessment | 9 |
4 |
3 |
12 |
9 |
5 |
1 |
0 |
2 |
0 |
1 |
0 |
46 |
| Invasion impacts and dynamics of a European‐wide introduced species | 9 |
8 |
17 |
4 |
9 |
8 |
3 |
2 |
3 |
1 |
1 |
1 |
66 |
| Iron in boreal river catchments : Biogeochemical, ecological and management implications | 9 |
8 |
10 |
14 |
10 |
14 |
7 |
5 |
3 |
1 |
2 |
3 |
86 |
| Is 15 % restoration sufficient to safeguard the habitats of boreal red-listed mire plant species? | 2 |
2 |
4 |
2 |
3 |
6 |
1 |
0 |
0 |
0 |
0 |
0 |
20 |
| Is catchment geodiversity a useful surrogate of aquatic plant species richness? | 5 |
6 |
9 |
11 |
9 |
12 |
1 |
0 |
1 |
0 |
0 |
1 |
55 |
| Isolated by lakes: the influence of connectivity on benthic macroinvertebrate community structure in river- and lake-connected streams | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Julkiset ruokapalvelut voivat toimia reilun ruokamurroksen edelläkävijöinä | 10 |
20 |
17 |
3 |
5 |
7 |
0 |
0 |
2 |
4 |
4 |
7 |
79 |
| Just destabilisation? Considering justice in the phase-out of peat | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Just Pathways to Sustainability: From Environmental Human Rights Defenders to Biosphere Defenders | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Kansallinen pölyttäjästrategia vahvistaa pölyttäjien suojelua | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Kaukokartoitus mahdollistaa tarkan tiedon tuottamisen metsäluonnon monimuotoisuutta ilmentävistä piirteistä | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Kestävän kaupunkikehityksen indikaattorit tehoavasti käyttöön | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
14 |
39 |
18 |
71 |
| Kinetics of arsenic and antimony reduction and oxidation in peatlands treating mining-affected waters : Effects of microbes, temperature, and carbon substrate | 6 |
6 |
6 |
4 |
2 |
6 |
0 |
1 |
2 |
1 |
2 |
0 |
36 |
| Knitting patterns of biodiversity, range size and body size in aquatic beetle faunas : significant relationships but slightly divergent drivers | 5 |
3 |
9 |
6 |
3 |
8 |
1 |
1 |
0 |
0 |
0 |
2 |
38 |
| Knowledge brokerage context factors - What matters in knowledge exchange in impact assessment? | 6 |
5 |
12 |
8 |
12 |
14 |
1 |
2 |
0 |
3 |
0 |
1 |
64 |
| Knowledge brokering at the environmental science-policy interface — examining structure and activity | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Knowledge co-production around the cormorant-fishing conflict using a joint fact-finding approach | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Kunnan toteuttamat ekologiset kompensaatiot: Kuka maksaa? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Kunnat hidastamaan luontokatoa : suosituksia luontohaittojen välttämiseksi, lieventämiseksi ja kompensoimiseksi kuntien maankäytössä | 0 |
0 |
0 |
0 |
28 |
26 |
5 |
7 |
4 |
8 |
7 |
7 |
92 |
| Kuntokato kuriin kaupunkisuunnittelulla | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
11 |
1 |
4 |
7 |
13 |
36 |
| Lake browning counteracts cyanobacteria responses to nutrients: Evidence from phytoplankton dynamics in large enclosure experiments and comprehensive observational data | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Lake restoration influences nutritional quality of algae and consequently Daphnia biomass | 0 |
5 |
7 |
6 |
4 |
8 |
1 |
1 |
0 |
1 |
0 |
0 |
33 |
| Lake restoration influences nutritional quality of algae and consequently Daphnia biomass | 2 |
5 |
18 |
1 |
3 |
8 |
1 |
2 |
0 |
0 |
0 |
0 |
40 |
| Lakes as nitrous oxide sources in the boreal landscape | 8 |
4 |
5 |
4 |
8 |
7 |
6 |
2 |
5 |
11 |
7 |
4 |
71 |
| Lakes in the era of global change : moving beyond single‐lake thinking in maintaining biodiversity and ecosystem services | 52 |
38 |
62 |
59 |
42 |
47 |
3 |
14 |
11 |
26 |
19 |
16 |
389 |
| Lakeshore areas of conservation interest: Characteristics of nursery areas of the threatened lake‐dwelling grayling, Thymallus thymallus | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Lakisääteisellä ilmastosuunnitelmalla uusia mahdollisuuksia kuntien ilmastotyöhön | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
5 |
2 |
4 |
1 |
0 |
12 |
| Land use change to reduce freshwater nitrogen and phosphorus will be effective even with projected climate change | 5 |
6 |
8 |
9 |
7 |
8 |
2 |
0 |
2 |
1 |
0 |
0 |
48 |
| Land use in acid sulphate soils degrades river water quality : Do the biological quality metrics respond? | 23 |
13 |
15 |
11 |
14 |
7 |
4 |
3 |
2 |
2 |
4 |
2 |
100 |
| Land-use change in a Nordic future towards bioeconomy: A methodological framework to compare and merge stakeholder and expert opinions on qualitative scenarios | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
4 |
2 |
3 |
12 |
| Land-use dominates climate controls on nitrogen and phosphorus export from managed and natural Nordic headwater catchments | 1 |
7 |
8 |
4 |
11 |
9 |
2 |
1 |
2 |
1 |
1 |
2 |
49 |
| Landscape and soundscape quality promote stress recovery in nearby urban nature: A multisensory field experiment | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Late flowering time enhances insect pollination of turnip rape | 7 |
4 |
10 |
12 |
9 |
8 |
3 |
2 |
3 |
0 |
0 |
4 |
62 |
| Learning and agency for sustainability transformations: building on Bandura’s theory of human agency | 18 |
15 |
24 |
8 |
20 |
11 |
2 |
2 |
2 |
4 |
2 |
8 |
116 |
| Legal and political arguments on aquatic ecosystem services and hydropower development – A case study on Kemi River basin, Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Lessons from COVID-19 for managing transboundary climate risks and building resilience | 4 |
7 |
3 |
6 |
13 |
7 |
1 |
2 |
0 |
0 |
0 |
1 |
44 |
| Leverage points for sustainability transformation: Identifying past and future changes in the Finnish (circular) plastic packing system | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Lichen communities on Populus tremula are affected by the density of Picea abies | 3 |
4 |
9 |
15 |
9 |
9 |
3 |
4 |
1 |
0 |
0 |
1 |
58 |
| Linear, reuse or recycling? : An environmental comparison of different life cycle options for cotton roller towels | 16 |
10 |
7 |
6 |
10 |
9 |
4 |
2 |
4 |
6 |
2 |
4 |
80 |
| Linking natural capital stocks with ecosystem services in the Northern Baltic Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Linking pollinator occurrence in field margins to pollinator visitation to a mass-flowering crop | 4 |
8 |
6 |
11 |
19 |
17 |
8 |
6 |
16 |
9 |
2 |
8 |
114 |
| Literature syntheses to inform marine ecosystem management: lessons learned from stakeholder participation | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
43 |
34 |
0 |
1 |
78 |
| Little evidence of range size conservatism in freshwater plants across two continents | 10 |
6 |
7 |
9 |
5 |
10 |
1 |
0 |
0 |
0 |
1 |
1 |
50 |
| Local adaptation through countergradient selection in northern populations of Skeletonema marinoi | 4 |
6 |
16 |
14 |
16 |
11 |
2 |
3 |
0 |
0 |
0 |
1 |
73 |
| Local adaptation to climate anomalies relates to species phylogeny | 4 |
7 |
7 |
8 |
6 |
6 |
1 |
3 |
1 |
0 |
0 |
0 |
43 |
| Long-term ice phenology records spanning up to 578 years for 78 lakes around the Northern Hemisphere | 4 |
3 |
10 |
3 |
9 |
8 |
1 |
3 |
0 |
0 |
0 |
1 |
42 |
| Long-term nitrogen and phosphorus dynamics in waters discharging from forestry-drained and undrained boreal peatlands | 8 |
4 |
9 |
5 |
5 |
4 |
2 |
1 |
3 |
3 |
2 |
1 |
47 |
| Low-level retention forestry, certification, and biodiversity : case Finland | 4 |
9 |
8 |
2 |
13 |
9 |
3 |
2 |
3 |
0 |
6 |
7 |
66 |
| Luontotieto ja sen käyttö kestävyysmurroksessa: Havaintoja vakiintuneilta ja nousevilta toimijoilta Suomessa | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Lähivihreän hyvinvointivaikutukset –tietopaketti | 17 |
17 |
9 |
14 |
11 |
7 |
1 |
8 |
4 |
8 |
6 |
4 |
106 |
| Lämpövarastot ja hukkalämpö -avaimia energiakriisiin | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
2 |
7 |
10 |
| Lääkeaineiden ympäristöriskin arvioinnin epävarmuuslähteitä | 0 |
2 |
7 |
9 |
9 |
7 |
5 |
2 |
2 |
2 |
1 |
1 |
47 |
| Machine learning based analysis of Finnish World War II photographers | 7 |
5 |
11 |
7 |
3 |
7 |
0 |
3 |
2 |
0 |
2 |
5 |
52 |
| Macro-turbulent flow and its impacts on sediment transport potential of a subarctic river during ice-covered and open-channel conditions | 4 |
2 |
13 |
2 |
10 |
9 |
2 |
2 |
1 |
1 |
1 |
1 |
48 |
| Macroalgae production in Northern Europe : Business and government perspectives on how to regulate a novel blue bioeconomy | 34 |
10 |
8 |
6 |
7 |
14 |
4 |
17 |
1 |
0 |
2 |
3 |
106 |
| Macroecology of ground beetles : Species richness, range size and body size show different geographical patterns across a climatically heterogeneous area | 1 |
3 |
12 |
6 |
6 |
13 |
1 |
1 |
0 |
1 |
0 |
0 |
44 |
| Macroecology of macrophytes in the freshwater realm : Patterns, mechanisms and implications | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Maintaining natural and traditional cultural green infrastructures across Europe : learning from historic and current landscape transformations | 4 |
7 |
8 |
1 |
5 |
11 |
2 |
1 |
1 |
0 |
2 |
0 |
42 |
| Make carbon footprints available – And it is not just one value | 9 |
5 |
4 |
8 |
5 |
4 |
0 |
0 |
0 |
6 |
2 |
0 |
43 |
| Making the circular economy online : a hyperlink analysis of the articulation of nutrient recycling in Finland | 8 |
9 |
13 |
9 |
11 |
10 |
1 |
3 |
1 |
0 |
1 |
0 |
66 |
| Mamiellophyceae shift in seasonal predominance in the Baltic Sea | 3 |
1 |
7 |
3 |
9 |
12 |
3 |
2 |
2 |
3 |
3 |
1 |
49 |
| Management plans as resources in conservation conflicts | 8 |
3 |
9 |
1 |
7 |
12 |
0 |
5 |
2 |
2 |
2 |
2 |
53 |
| Mapping CO2 traffic emissions within local climate zones in Helsinki | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Mapping Europe’s institutional landscape for forest ecosystem service provision, innovations and governance | 4 |
4 |
9 |
2 |
7 |
6 |
6 |
1 |
3 |
0 |
1 |
1 |
44 |
| Mapping hotspots and bundles of forest ecosystem services across the European Union | 6 |
3 |
5 |
5 |
6 |
10 |
3 |
6 |
1 |
1 |
1 |
1 |
48 |
| Mapping suspended sediment dynamics in the Pantanal wetland using remote sensing and ANN-based models | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
3 |
6 |
| Mapping the dependence of black carbon radiative forcing on emission region and season | 14 |
15 |
18 |
8 |
10 |
11 |
55 |
54 |
1 |
3 |
1 |
5 |
195 |
| Mapping two centuries of forest governance in Nordic countries: An open access database | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Maps of light pollution in odd places : Are night time satellite pictures making us to forget natural darkness? | 6 |
9 |
7 |
4 |
9 |
15 |
2 |
2 |
5 |
2 |
1 |
0 |
62 |
| Marine connectivity in spatial conservation planning : analogues from the terrestrial realm | 6 |
3 |
11 |
6 |
11 |
10 |
2 |
1 |
3 |
0 |
3 |
0 |
56 |
| Marine ecosystem extent and condition pilot accounts for Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Marine monitoring in transition : On the verge of technological revolution? | 0 |
0 |
27 |
364 |
22 |
43 |
19 |
4 |
1 |
0 |
0 |
0 |
480 |
| Marine Stewardship Council Certification in Finland and Russia: Global Standards and Local Practices | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
1 |
| Market intermediation and its embeddeness : Lessons from the Finnish energy transition | 14 |
9 |
13 |
7 |
7 |
7 |
2 |
4 |
2 |
2 |
0 |
1 |
68 |
| Measuring the spatiotemporal variability in snow depth in subarctic environments using UASs – Part 2: Snow processes and snow–canopy interactions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Mechanisms underpinning community stability along a latitudinal gradient: Insights from a niche‐based approach | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
23 |
8 |
5 |
36 |
| Meeting places and social capital supporting rural landscape stewardship : A Pan-European horizon scanning | 9 |
11 |
18 |
17 |
21 |
13 |
6 |
11 |
6 |
5 |
1 |
16 |
134 |
| Megaphylogeny resolves global patterns of mushroom evolution | 4 |
3 |
13 |
4 |
9 |
7 |
2 |
5 |
2 |
0 |
2 |
1 |
52 |
| Meta-analysis of multidecadal biodiversity trends in Europe | 2 |
3 |
7 |
3 |
8 |
7 |
3 |
4 |
4 |
2 |
2 |
0 |
45 |
| Metacommunity ecology meets bioassessment : Assessing spatio-temporal variation in multiple facets of macroinvertebrate diversity in human-influenced large lakes | 10 |
2 |
10 |
8 |
8 |
12 |
0 |
4 |
1 |
2 |
2 |
1 |
60 |
| Metagenome-assembled genomes from mineral tundra soils in Rásttigáisá, northern Norway | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Metal sourcing for a sustainable future | 13 |
8 |
14 |
6 |
11 |
8 |
4 |
3 |
3 |
0 |
1 |
4 |
75 |
| Methodological interlinkages for mapping ecosystem services - from data to analysis and decision-support | 5 |
2 |
7 |
1 |
5 |
9 |
1 |
5 |
7 |
3 |
5 |
0 |
50 |
| Methodology for prioritizing marine environmental pressures under various management scenarios in the Black Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Metsäojitettujen soiden typpi- ja fosforikuormitus Suomessa | 6 |
5 |
7 |
6 |
10 |
11 |
4 |
1 |
1 |
2 |
1 |
0 |
54 |
| Metsäojitettujen soiden vesistökuormitus | 5 |
11 |
7 |
4 |
14 |
5 |
2 |
2 |
1 |
1 |
2 |
8 |
62 |
| Microbial remineralization processes during postspring-bloom with excess phosphate available in the northern Baltic Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Microclimatic variability buffers butterfly populations against increased mortality caused by phenological asynchrony between larvae and their host plants | 6 |
5 |
4 |
4 |
7 |
8 |
0 |
0 |
1 |
0 |
0 |
1 |
36 |
| Microplastic concentrations, size distribution, and polymer types in the surface waters of a northern European lake | 12 |
3 |
7 |
6 |
11 |
8 |
89 |
2 |
3 |
5 |
4 |
2 |
152 |
| Microplastic ingestion by small coastal fish in the northern Baltic Sea, Finland | 11 |
7 |
6 |
5 |
7 |
7 |
2 |
1 |
0 |
1 |
0 |
1 |
48 |
| Microplastics accumulate to thin layers in the stratified Baltic Sea | 8 |
0 |
3 |
5 |
6 |
2 |
1 |
3 |
0 |
1 |
0 |
0 |
29 |
| Microplastics originated from agricultural mulching films affect enchytraeid multigeneration reproduction and soil properties | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Microplastics pollution in the Brahmaputra River and the Indus River of the Indian Himalaya | 5 |
7 |
23 |
18 |
15 |
11 |
6 |
14 |
5 |
7 |
6 |
6 |
123 |
| Microplastics, chlorpyrifos and their mixtures modulate immune processes in the terrestrial crustacean Porcellio scaber | 3 |
8 |
5 |
2 |
6 |
8 |
1 |
2 |
3 |
4 |
4 |
2 |
48 |
| Micropollutants in urban wastewater : large-scale emission estimates and analysis of measured concentrations in the Baltic Sea catchment | 11 |
12 |
17 |
15 |
9 |
10 |
1 |
4 |
2 |
0 |
1 |
2 |
84 |
| Mind the income gap: Income from wood production exceed income from providing diverse ecosystem services from Europe’s forests | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Mining in the newspapers : local and regional media representations of mineral exploration and mining in Finland, Germany, and Spain | 5 |
4 |
2 |
3 |
8 |
3 |
1 |
2 |
1 |
0 |
1 |
0 |
30 |
| Mining through controversies : Public perceptions and the legitimacy of a planned gold mine near a tourist destination | 9 |
9 |
13 |
22 |
11 |
15 |
1 |
1 |
1 |
89 |
39 |
0 |
210 |
| Mismatch, empowerment, fatigue or balance? Four scenarios of physical activity up to 2030 in Finland | 20 |
12 |
10 |
5 |
8 |
8 |
1 |
2 |
0 |
1 |
0 |
1 |
68 |
| Mistä lääkettä kestävyysvetkutteluun? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
55 |
9 |
1 |
6 |
4 |
75 |
| Miten voitaisiin vähentää muovisten, kertakäyttöisten take away -elintarvikepakkausten kulutusta | 4 |
7 |
5 |
6 |
13 |
7 |
1 |
1 |
0 |
1 |
2 |
0 |
47 |
| Mixed effects of a national protected area network on terrestrial and freshwater biodiversity | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
8 |
3 |
1 |
12 |
| Modeling soil organic carbon dynamics in temperate forests with Yasso07 | 6 |
3 |
7 |
4 |
5 |
8 |
2 |
2 |
2 |
2 |
2 |
0 |
43 |
| Modeling water quality in the Anthropocene : directions for the next-generation aquatic ecosystem models | 5 |
9 |
9 |
3 |
7 |
11 |
2 |
0 |
1 |
0 |
1 |
1 |
49 |
| Modelling climate change impacts on lake ice and snow demonstrates breeding habitat decline of the endangered Saimaa ringed seal | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Modelling cycling to school in Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Modelling population structure in the context of urban land use change in Europe | 8 |
3 |
6 |
5 |
5 |
10 |
2 |
1 |
4 |
2 |
4 |
2 |
52 |
| Modelling the gas–particle partitioning and water uptake of isoprene-derived secondary organic aerosol at high and low relative humidity | 4 |
3 |
7 |
2 |
2 |
6 |
0 |
1 |
2 |
0 |
1 |
1 |
29 |
| Modelling the impacts of intensifying forest management on carbon budget across a long latitudinal gradient in Europe | 3 |
2 |
8 |
4 |
6 |
6 |
5 |
2 |
0 |
0 |
2 |
2 |
40 |
| Model‐based variance partitioning for statistical ecology | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Modulation of chlorpyrifos toxicity to soil arthropods by simultaneous exposure to polyester microfibers or tire particle microplastics | 19 |
8 |
16 |
5 |
14 |
10 |
1 |
2 |
1 |
3 |
1 |
3 |
83 |
| Molecular versus morphological data for benthic diatoms biomonitoring in Northern Europe freshwater and consequences for ecological status | 13 |
7 |
7 |
5 |
6 |
15 |
11 |
4 |
3 |
4 |
1 |
0 |
76 |
| Monipaikkaisuuden ja paikkariippumattomuuden vaikutukset alue- ja yhdyskuntarakenteeseen | 0 |
0 |
0 |
0 |
44 |
31 |
4 |
3 |
1 |
4 |
5 |
5 |
97 |
| Monitoring a changing Arctic : Recent advancements in the study of sea ice microbial communities | 3 |
4 |
9 |
7 |
6 |
6 |
2 |
2 |
0 |
0 |
0 |
0 |
39 |
| Monitoring and modelling of butyltin compounds in Finnish inland lake | 0 |
0 |
0 |
0 |
48 |
18 |
4 |
5 |
4 |
0 |
0 |
1 |
80 |
| Monitoring changes in boreal peatland vegetation after restoration with optical satellite imagery | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Monitoring changes in forestry and seasonal snow using surface albedo during 1982-2016 as an indicator | 6 |
3 |
6 |
6 |
6 |
5 |
3 |
1 |
1 |
0 |
1 |
1 |
39 |
| Monitoring of sessile and mobile epifauna – Considerations for non-indigenous species | 11 |
8 |
6 |
5 |
4 |
6 |
0 |
1 |
0 |
0 |
0 |
2 |
43 |
| More wood but less biodiversity in forests in Finland : a historical evaluation | 21 |
5 |
3 |
7 |
6 |
4 |
4 |
9 |
17 |
22 |
50 |
8 |
156 |
| Morphological traits predict host-tree specialization in wood-inhabiting fungal communities | 9 |
10 |
14 |
13 |
12 |
16 |
3 |
9 |
14 |
4 |
14 |
5 |
123 |
| Moving beyond disruptive innovation : A review of disruption in sustainability transitions | 13 |
19 |
10 |
14 |
17 |
14 |
40 |
39 |
6 |
5 |
2 |
5 |
184 |
| Multi-Criteria Decision Analysis and Cost-Benefit Analysis : Comparing alternative frameworks for integrated valuation of ecosystem services | 36 |
28 |
33 |
39 |
41 |
39 |
27 |
40 |
14 |
27 |
36 |
26 |
386 |
| Multi-level responses of Macoma balthica to recurring hypoxic disturbance | 10 |
3 |
6 |
8 |
8 |
8 |
1 |
2 |
3 |
3 |
1 |
2 |
55 |
| Multimethod valuation of peatland ecosystem services : Combining choice experiment, multicriteria decision analysis and deliberative valuation | 17 |
9 |
11 |
10 |
14 |
10 |
3 |
1 |
2 |
4 |
7 |
0 |
88 |
| Multimodal subspace support vector data description | 3 |
7 |
14 |
10 |
6 |
11 |
1 |
4 |
2 |
2 |
2 |
0 |
62 |
| Multiple anthropogenic drivers behind upward trends in organic carbon concentrations in boreal rivers | 4 |
3 |
11 |
6 |
11 |
6 |
3 |
3 |
4 |
1 |
8 |
5 |
65 |
| Multiple facets of stream macroinvertebrate alpha diversity are driven by different ecological factors across an extensive altitudinal gradient | 7 |
1 |
8 |
5 |
4 |
7 |
0 |
1 |
0 |
3 |
3 |
1 |
40 |
| Multiple stressors in small streams in the forestry context of Fennoscandia : The effects in time and space | 6 |
4 |
4 |
7 |
8 |
5 |
0 |
1 |
2 |
0 |
0 |
3 |
40 |
| Multiscale Cloud Detection in Remote Sensing Images Using a Dual Convolutional Neural Network | 1 |
10 |
12 |
9 |
12 |
20 |
2 |
1 |
2 |
1 |
5 |
7 |
82 |
| Multitrophic biodiversity patterns and environmental descriptors of sub‐Arctic lakes in northern Europe | 3 |
3 |
9 |
2 |
6 |
6 |
0 |
3 |
1 |
1 |
1 |
2 |
37 |
| Municipal climate communication as a tool in amplifying local climate action and developing a place brand | 5 |
9 |
17 |
10 |
21 |
16 |
8 |
55 |
2 |
1 |
2 |
2 |
148 |
| Municipal experimental policy engagements in the built environment | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Muovit ja niiden vaikutukset maaympäristössä | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
5 |
6 |
8 |
9 |
28 |
| Mussel caging and the weight of evidence approach in the assessment of chemical contamination in coastal waters of Finland (Baltic Sea) | 10 |
0 |
10 |
3 |
3 |
4 |
1 |
1 |
0 |
1 |
0 |
0 |
33 |
| Muted by a crisis? COVID-19 and the long-term evolution of climate change newspaper coverage | 4 |
11 |
16 |
8 |
4 |
9 |
3 |
0 |
2 |
0 |
0 |
1 |
58 |
| Mökkitutkimuksesta monipaikkaisuuteen ja etätyömatkailuun: vapaa-ajan asumisen tutkimus 2000-luvulla | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| National assessment on the status, trends and impacts of marine non-indigenous species for the European Union marine strategy framework directive | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Nationally reported metrics can’t adequately guide transformative change in biodiversity policy | 4 |
3 |
9 |
2 |
11 |
11 |
2 |
3 |
1 |
0 |
1 |
1 |
48 |
| Nature-issues: Ecosystem restoration as a reorganiser of social–material relations | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Nature’s nocturnal services: Light pollution as a non-recognised challenge for ecosystem services research and management | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Navigating the pathway from collaborative governance to impacts under uncertainty: A theory of change for watershed visions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Navigating the science-policy interface: Forest researcher perspectives | 8 |
5 |
8 |
5 |
11 |
14 |
65 |
11 |
7 |
4 |
5 |
6 |
149 |
| Near-term climate impacts of Finnish residential wood combustion | 10 |
10 |
8 |
3 |
5 |
8 |
1 |
2 |
0 |
1 |
0 |
1 |
49 |
| Neglected dipterans in stream studies | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Network Analysis of Energy Transition Arena Experiments | 8 |
11 |
10 |
13 |
11 |
11 |
5 |
3 |
6 |
3 |
10 |
5 |
96 |
| Networks at the science-policy-interface : Challenges, opportunities and the viability of the ‘network-of-networks’ approach | 4 |
2 |
9 |
6 |
9 |
15 |
0 |
3 |
3 |
3 |
5 |
3 |
62 |
| Next steps in the energy transition—a high-impact forum | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Niche position drives interspecific variation in occupancy and abundance in a highly-connected lake system | 2 |
3 |
7 |
3 |
2 |
9 |
3 |
0 |
1 |
3 |
1 |
2 |
36 |
| Niittyjen lajisto kärsii kasvillisuuden rehevöitymisestä | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Nitrogen and phosphorus losses in Nordic and Baltic agricultural monitoring catchments – Spatial and temporal variations in relation to natural conditions and mitigation programmes | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
7 |
2 |
4 |
13 |
| Nitrogen removal of mine-influenced water in a hybrid bioreactor with floating hook-moss (Warnstorfia fluitans) in cold climate conditions | 5 |
6 |
9 |
8 |
7 |
11 |
2 |
1 |
3 |
1 |
4 |
0 |
57 |
| No biotic homogenisation across decades but consistent effects of landscape position and pH on macrophyte communities in boreal lakes | 3 |
1 |
7 |
3 |
3 |
4 |
0 |
1 |
0 |
0 |
0 |
3 |
25 |
| Non-indigenous species refined national baseline inventories : A synthesis in the context of the European Union's Marine Strategy Framework Directive | 8 |
4 |
9 |
3 |
4 |
5 |
1 |
1 |
1 |
1 |
0 |
2 |
39 |
| Nordic hydrological frontier in the 21st century | 5 |
9 |
17 |
7 |
7 |
11 |
1 |
4 |
3 |
0 |
4 |
1 |
69 |
| Nordic socio-recreational ecosystem services in a hydropeaked river | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Novel methods for spatial prioritization with applications in conservation, land use planning and ecological impact avoidance | 6 |
14 |
15 |
12 |
11 |
14 |
2 |
2 |
1 |
4 |
6 |
4 |
91 |
| Numerical simulation and evaluation of global ultrafine particle concentrations at the Earth's surface | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Nutrient enrichment homogenizes taxonomic and functional diversity of benthic macroinvertebrate assemblages in shallow lakes | 12 |
7 |
8 |
7 |
14 |
10 |
7 |
3 |
6 |
2 |
4 |
3 |
83 |
| Nutrient load mitigation with wintertime cover as estimated by the INCA model | 0 |
1 |
6 |
3 |
1 |
7 |
1 |
1 |
1 |
1 |
1 |
0 |
23 |
| Ocean integration : The needs and challenges of effective coordination within the ocean observing system | 7 |
6 |
2 |
4 |
8 |
6 |
0 |
1 |
1 |
0 |
0 |
1 |
36 |
| Oil degradation potential of microbial communities in water and sediment of Baltic Sea coastal area | 5 |
4 |
8 |
4 |
7 |
7 |
1 |
0 |
3 |
1 |
0 |
2 |
42 |
| On Sistotremastrum and similar-looking taxa (Trechisporales, Basidiomycota) | 8 |
5 |
7 |
1 |
10 |
15 |
2 |
3 |
8 |
2 |
5 |
3 |
69 |
| On the trade-offs and synergies between forest carbon sequestration and substitution | 4 |
6 |
13 |
15 |
14 |
9 |
7 |
4 |
2 |
1 |
0 |
2 |
77 |
| Ongoing fen–bog transition in a boreal aapa mire inferred from repeated field sampling, aerial Images, and Landsat data | 8 |
5 |
9 |
9 |
7 |
10 |
4 |
4 |
3 |
2 |
4 |
6 |
71 |
| Ontological conflict over forests in Inari/Aanaar: Sámi’s fight for preservation and renewal | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Ontological struggle over new product category : Transition potential of meat alternatives | 98 |
10 |
11 |
3 |
10 |
10 |
1 |
4 |
0 |
2 |
3 |
2 |
154 |
| Opportunities and limitations of carbon footprint calculators to steer sustainable household consumption – Analysis of Nordic calculator features | 25 |
18 |
28 |
42 |
29 |
28 |
21 |
19 |
16 |
14 |
12 |
18 |
270 |
| Optical model for the Baltic Sea with an explicit CDOM state variable : a case study with Model ERGOM (version 1.2) | 2 |
2 |
10 |
14 |
5 |
6 |
1 |
1 |
1 |
0 |
3 |
1 |
46 |
| Optical Monitoring of Microplastics Filtrated from Wastewater Sludge and Suspended in Ethanol | 5 |
6 |
12 |
15 |
12 |
8 |
7 |
1 |
5 |
5 |
4 |
8 |
88 |
| Oral exposure to thiacloprid-based pesticide (Calypso SC480) causes physical poisoning symptoms and impairs the cognitive abilities of bumble bees | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
9 |
4 |
1 |
14 |
| Origin and fate of dissolved organic matter in four shallow Baltic Sea estuaries | 8 |
2 |
9 |
2 |
4 |
6 |
1 |
3 |
2 |
0 |
0 |
1 |
38 |
| Osaamisen kehittämistä ja verkostoitumista IFLAssa : poimintoja WLIC 2022 Dublinin konferenssista | 0 |
26 |
11 |
9 |
8 |
8 |
3 |
0 |
5 |
0 |
2 |
3 |
75 |
| Overview : Recent advances in the understanding of the northern Eurasian environments and of the urban air quality in China – a Pan-Eurasian Experiment (PEEX) programme perspective | 5 |
7 |
15 |
3 |
7 |
8 |
0 |
1 |
0 |
0 |
0 |
0 |
46 |
| Oxygen consumption rates and respiratory carbon losses in three species of copepods (Acartia clausi, Calanus helgolandicus and Limnocalanus macrurus) during starvation | 5 |
2 |
11 |
2 |
5 |
7 |
3 |
1 |
2 |
0 |
1 |
1 |
40 |
| Palsasoiden levinneisyys, rakennetyypit ja tila Suomessa 2010-luvulla | 0 |
0 |
0 |
0 |
19 |
22 |
8 |
123 |
49 |
17 |
32 |
10 |
280 |
| Parallel and comparative use of three multicriteria decision support methods in an environmental portfolio problem | 0 |
0 |
24 |
25 |
19 |
18 |
3 |
9 |
1 |
2 |
6 |
2 |
109 |
| Parenting in a changing environment: A long-term study of prolactin, parental effort and reproductive success in common eiders | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Participation for just governance of food-system transition | 4 |
7 |
10 |
5 |
9 |
13 |
1 |
1 |
1 |
1 |
1 |
2 |
55 |
| Participatory multi-criteria decision analysis in valuing peatland ecosystem services : Trade-offs related to peat extraction vs. pristine peatlands in Southern Finland | 8 |
8 |
7 |
10 |
14 |
6 |
0 |
3 |
4 |
0 |
0 |
3 |
63 |
| Particle balance and return loops for microplastics in a tertiary-level wastewater treatment plant | 0 |
7 |
5 |
1 |
9 |
10 |
2 |
2 |
0 |
3 |
1 |
1 |
41 |
| Particle fluxes by subtropical pelagic communities under ocean alkalinity enhancement | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Partition of marine environment dynamics according to remote sensing reflectance and relations of dynamics to physical factors | 8 |
6 |
33 |
3 |
2 |
9 |
0 |
4 |
1 |
3 |
2 |
0 |
71 |
| Partitioning of space among trees in an old-growth spruce forest in subarctic Fennoscandia | 13 |
0 |
19 |
11 |
11 |
12 |
2 |
2 |
1 |
1 |
1 |
2 |
75 |
| Passing the baton : How intermediaries advance sustainability transitions in different phases | 12 |
5 |
5 |
8 |
10 |
8 |
3 |
1 |
3 |
0 |
0 |
2 |
57 |
| Peatland drainage - a missing link behind increasing TOC concentrations in waters from high latitude forest catchments? | 9 |
5 |
6 |
1 |
4 |
5 |
1 |
0 |
1 |
3 |
0 |
5 |
40 |
| PEFC- ja FSC-metsäsertifiointistandardien vertailu sekä ekologinen vaikuttavuus lainsäädännön ja tutkimustiedon valossa | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Pelkkä ekologinen kompensaatio ei takaa ekologisesti kestävää maankäyttöä : Kommentti Hytösen ja Tupalan artikkeliin | 0 |
0 |
18 |
16 |
15 |
17 |
0 |
0 |
1 |
0 |
1 |
4 |
72 |
| Perceived wellbeing effects of ecosystems in Finland | 2 |
1 |
10 |
3 |
10 |
12 |
0 |
3 |
1 |
0 |
1 |
1 |
44 |
| Performance of constructed fish spawning and rearing channels – development of the Imatra City Brook in Finland | 13 |
10 |
11 |
4 |
15 |
11 |
3 |
3 |
1 |
3 |
2 |
2 |
78 |
| Pesticide residues in honeybee-collected pollen : does the EU regulation protect honeybees from pesticides? | 7 |
6 |
6 |
17 |
7 |
10 |
4 |
2 |
2 |
1 |
1 |
1 |
64 |
| PFASs in Finnish rivers and fish and the loading of PFASs to the Baltic Sea | 7 |
9 |
10 |
6 |
6 |
7 |
1 |
1 |
0 |
4 |
2 |
2 |
55 |
| Pharmaceutical residues in plastic tablet containers: Impacts on recycling and the environment | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Phosphorus exchange in eutrophied coastal brackish water sediments - sorption pattern, potential and factors affecting them | 2 |
7 |
10 |
12 |
22 |
13 |
3 |
7 |
2 |
11 |
2 |
5 |
96 |
| Physical oceanography sets the scene for the Marine Strategy Framework Directive implementation in the Baltic Sea | 5 |
6 |
8 |
5 |
4 |
11 |
1 |
1 |
3 |
3 |
2 |
3 |
52 |
| Physicochemical and isotopic similarity between well water and intruding surface water is not synonymous with similarity in prokaryotic diversity and community composition | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Phytoflagellate diversity in Roskilde Fjord (Denmark), including the description of Pyramimonas octopora sp. nov. (Pyramimonadales, Chlorophyta) | 2 |
5 |
14 |
2 |
4 |
7 |
1 |
1 |
2 |
2 |
0 |
3 |
43 |
| Phytoplankton bloom dynamics in the Baltic Sea using a consistently reprocessed time series of multi-sensor reflectance and novel Chlorophyll-a retrievals | 5 |
6 |
7 |
9 |
4 |
10 |
4 |
0 |
1 |
0 |
0 |
3 |
49 |
| Phytoplankton species richness along coastal and estuarine salinity continua | 5 |
4 |
17 |
7 |
10 |
8 |
2 |
3 |
4 |
2 |
5 |
0 |
67 |
| PIMA-ala kehittyy, missä olemme viiden vuoden kuluttua? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Pioneering farmers value agronomic performance of cover crops and their impacts on soil and environment | 7 |
4 |
9 |
37 |
10 |
9 |
2 |
2 |
4 |
3 |
2 |
0 |
89 |
| Pluralising agency to understand behaviour change in sustainability transitions | 10 |
2 |
14 |
5 |
9 |
11 |
2 |
1 |
2 |
1 |
1 |
1 |
59 |
| Policy and political (in)coherence, security and Nordic–Baltic energy transitions | 0 |
0 |
15 |
6 |
11 |
6 |
0 |
1 |
2 |
0 |
1 |
3 |
45 |
| Policy coherence for ecosystem-based management: Implementing EU water and marine policies in the Archipelago Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Policy mixes for more vital legume value chains: Evaluation across competing policy frames | 4 |
1 |
1 |
5 |
8 |
3 |
1 |
1 |
1 |
0 |
2 |
0 |
27 |
| Policy-driven monitoring and evaluation : Does it support adaptive management of socio-ecological systems? | 7 |
5 |
6 |
4 |
5 |
7 |
3 |
2 |
2 |
3 |
5 |
0 |
49 |
| Politics of knowledge use : epistemic governance in marine spatial planning | 0 |
0 |
19 |
10 |
14 |
11 |
2 |
6 |
7 |
2 |
3 |
1 |
75 |
| Polycyclic aromatic hydrocarbon sorption and bacterial community composition of biodegradable and conventional plastics incubated in coastal sediments | 4 |
8 |
14 |
3 |
7 |
12 |
3 |
0 |
2 |
3 |
0 |
2 |
58 |
| Post‐drainage stand growth and peat mineralization impair water quality from forested peatlands | 6 |
11 |
10 |
3 |
3 |
9 |
2 |
1 |
1 |
0 |
2 |
4 |
52 |
| Potential impacts of a future Nordic bioeconomy on surface water quality | 3 |
3 |
5 |
3 |
3 |
9 |
0 |
0 |
4 |
0 |
0 |
0 |
30 |
| Precision, Applicability, and Economic Implications : A Comparison of Alternative Biodiversity Offset Indexes | 5 |
19 |
13 |
1 |
4 |
5 |
3 |
0 |
4 |
1 |
1 |
1 |
57 |
| Predictable shifts in diversity and ecosystem function in phytoplankton communities along coastal salinity continua | 0 |
0 |
23 |
24 |
16 |
12 |
2 |
2 |
2 |
3 |
1 |
0 |
85 |
| Predicting discharge capacity of vegetated compound channels : uncertainty and identifiability of one-dimensional process-based models | 3 |
1 |
5 |
3 |
5 |
9 |
7 |
2 |
4 |
13 |
5 |
4 |
61 |
| Predicting hotspots for threatened plant species in boreal peatlands | 3 |
7 |
10 |
7 |
2 |
8 |
5 |
1 |
1 |
0 |
0 |
0 |
44 |
| Predicting valuable forest habitats using an indicator species for biodiversity | 10 |
11 |
10 |
3 |
8 |
7 |
1 |
2 |
4 |
4 |
5 |
4 |
69 |
| Primary production, carbon release, and respiration during spring bloom in the Baltic Sea | 3 |
4 |
6 |
2 |
8 |
10 |
1 |
1 |
2 |
0 |
2 |
2 |
41 |
| Priorities for social science and humanities research on the challenges of moving beyond animal-based food systems | 8 |
7 |
9 |
2 |
5 |
8 |
1 |
1 |
0 |
2 |
1 |
1 |
45 |
| Probabilistic ecological risk assessment for deep‐sea mining: A Bayesian network for Chatham Rise, Pacific Ocean | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Promise and performance of agricultural nutrient management policy : Lessons from the Baltic Sea | 5 |
4 |
3 |
5 |
7 |
5 |
0 |
1 |
1 |
0 |
0 |
0 |
31 |
| Promises of meat and milk alternatives : an integrative literature review on emergent research themes | 4 |
4 |
9 |
5 |
5 |
9 |
0 |
1 |
2 |
0 |
2 |
1 |
42 |
| Promoting sustainable energy : Does institutional entrepreneurship help? | 16 |
6 |
6 |
4 |
7 |
7 |
4 |
2 |
2 |
2 |
4 |
6 |
66 |
| Prospects for environmental communication based on 25 years of newspaper coverage of climate change and eutrophication in Finland | 4 |
6 |
3 |
5 |
7 |
12 |
1 |
0 |
1 |
0 |
0 |
1 |
40 |
| Protected freshwater ecosystem with incessant cyanobacterial blooming awaiting a resolution | 4 |
3 |
6 |
1 |
7 |
8 |
2 |
3 |
3 |
3 |
6 |
5 |
51 |
| Protecting and restoring Europe's waters : An analysis of the future development needs of the Water Framework Directive | 9 |
7 |
8 |
2 |
7 |
7 |
0 |
0 |
1 |
0 |
0 |
0 |
41 |
| Pulling biodiversity offsetting in different directions – Stakeholder frames in the preparation of the Finnish nature conservation act | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
9 |
6 |
2 |
17 |
| Quantification of an adverse outcome pathway network by bayesian regression and bayesian network modeling | 4 |
2 |
4 |
2 |
4 |
10 |
2 |
3 |
1 |
2 |
1 |
1 |
36 |
| Quantification of different microplastic fibres discharged from textiles in machine wash and tumble drying | 5 |
2 |
1 |
1 |
12 |
3 |
0 |
0 |
1 |
1 |
0 |
0 |
26 |
| Quantifying impacts of human pressures on ecosystem services : Effects of widespread non-indigenous species in the Baltic Sea | 24 |
12 |
14 |
14 |
20 |
13 |
4 |
3 |
2 |
0 |
1 |
1 |
108 |
| Quantifying the climate exposure of priority habitat constrained to specific environmental conditions : Boreal aapa mires | 19 |
11 |
17 |
6 |
12 |
30 |
3 |
2 |
0 |
0 |
5 |
5 |
110 |
| Rakennusten elinkaariominaisuudet | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
2 |
0 |
0 |
3 |
| Rapid quantification of microalgae growth with hyperspectral camera and vegetation indices | 5 |
5 |
12 |
7 |
16 |
8 |
5 |
8 |
2 |
4 |
1 |
1 |
74 |
| Rare Exports : Irony about Northern nature and commercialized culture | 5 |
7 |
6 |
7 |
5 |
7 |
0 |
0 |
1 |
1 |
1 |
2 |
42 |
| Rarity in freshwater vascular plants across Europe and North America : Patterns, mechanisms and future scenarios | 0 |
0 |
0 |
0 |
18 |
8 |
2 |
1 |
2 |
2 |
5 |
3 |
41 |
| Recent developments in second home research: has the COVID-19 pandemic spurred a re-thinking of second home mobilities? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Recent lateral expansion of Sphagnum bogs over central fen areas of boreal aapa mire complexes | 16 |
4 |
10 |
11 |
17 |
27 |
3 |
5 |
2 |
3 |
2 |
1 |
101 |
| Recent range shifts of moths, butterflies, and birds are driven by the breadth of their climatic niche | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Recognition of differences in the capacity to deal with floods—A cross‐country comparison of flood risk management | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Reconfigurations in sustainability transitions : a systematic and critical review | 9 |
8 |
24 |
31 |
17 |
17 |
3 |
5 |
4 |
1 |
2 |
3 |
124 |
| Recreational land use contributes to the loss of marine biodiversity | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Redox potential as a soil health indicator – how does it compare to microbial activity and soil structure? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Reducing redundancy in the bottleneck representation of autoencoders | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Refined estimates of water transport through the Åland Sea in the Baltic Sea | 4 |
1 |
1 |
1 |
8 |
4 |
1 |
0 |
0 |
0 |
0 |
0 |
20 |
| Reflectance variation in boreal landscape during the snow melting period using airborne imaging spectroscopy | 2 |
6 |
9 |
3 |
12 |
7 |
2 |
0 |
6 |
5 |
5 |
3 |
60 |
| Reflexive use of methods: a framework for navigating different types of knowledge and power in transformative research | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Regulations on insects as food and feed : a global comparison | 15 |
21 |
14 |
49 |
21 |
19 |
0 |
12 |
11 |
26 |
20 |
7 |
215 |
| Remineralization rate of terrestrial DOC as inferred from CO2 supersaturated coastal waters | 4 |
6 |
7 |
4 |
6 |
8 |
4 |
5 |
5 |
1 |
2 |
4 |
56 |
| Renewable energy in the news : Environmental, economic, policy and technology discussion of biogas | 4 |
7 |
18 |
5 |
5 |
4 |
5 |
0 |
3 |
2 |
1 |
0 |
54 |
| Renovation results of Finnish single-family renovation subsidies : Oil boiler replacement with heat pumps | 12 |
15 |
19 |
6 |
13 |
11 |
2 |
41 |
0 |
1 |
2 |
4 |
126 |
| Reproduction, growth and oxidative stress in earthworm Eisenia andrei exposed to conventional and biodegradable mulching film microplastics | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Reproductive rate of a top predator, the grey seal, as an indicator of the changes in the Baltic food web | 8 |
4 |
7 |
2 |
2 |
6 |
0 |
2 |
0 |
2 |
1 |
0 |
34 |
| Research challenges for cultural ecosystem services and public health in (peri-)urban environments | 18 |
32 |
34 |
35 |
15 |
17 |
3 |
1 |
9 |
6 |
10 |
2 |
182 |
| Research Infrastructure Contact Zones : a framework and dataset to characterise the activities of major biodiversity informatics initiatives | 10 |
6 |
10 |
5 |
11 |
11 |
5 |
4 |
2 |
0 |
1 |
2 |
67 |
| Residential solar power profitability with thermal energy storage and carbon-corrected electricity prices | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Residential wood combustion in Finland : PM2.5 emissions and health impacts with and without abatement measures | 7 |
3 |
9 |
3 |
6 |
8 |
1 |
1 |
6 |
0 |
0 |
0 |
44 |
| Resilient urban water services for the 21th century society : Stakeholder survey in Finland | 9 |
7 |
13 |
6 |
7 |
11 |
3 |
4 |
1 |
0 |
0 |
0 |
61 |
| Respiration rate scales inversely with sinking speed of settling marine aggregates | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
7 |
1 |
2 |
10 |
| Responses in growth and emissions of biogenic volatile organic compounds in Scots pine, Norway spruce and silver birch seedlings to different warming treatments in a controlled field experiment | 4 |
5 |
7 |
4 |
7 |
13 |
3 |
4 |
2 |
1 |
1 |
1 |
52 |
| Responses of coastal fishery resources to rapid environmental changes | 6 |
3 |
10 |
6 |
7 |
5 |
2 |
3 |
1 |
0 |
0 |
0 |
43 |
| Responses of the fish community in a eutrophicated lake to long-term food web management assessed by multiple sampling methods | 3 |
2 |
7 |
3 |
5 |
5 |
0 |
97 |
1 |
0 |
0 |
0 |
123 |
| Rethinking decision support under conditions of irreducible uncertainty : Co-designing a serious game to navigate Baltic Sea nutrient enrichment | 8 |
3 |
7 |
4 |
3 |
7 |
2 |
2 |
2 |
2 |
3 |
3 |
46 |
| Reviewing peatland forestry: Implications and mitigation measures for freshwater ecosystem browning | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
113 |
0 |
4 |
117 |
| Reviews and syntheses : Arctic fire regimes and emissions in the 21st century | 4 |
9 |
5 |
6 |
6 |
8 |
1 |
2 |
3 |
1 |
1 |
2 |
48 |
| Revisiting global trends in freshwater insect biodiversity | 2 |
4 |
3 |
5 |
9 |
2 |
0 |
0 |
1 |
0 |
0 |
0 |
26 |
| Rewetting on agricultural peatlands can offer cost effective greenhouse gas reduction at the national level | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Rights of the child as imperatives for transforming food systems | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Riparian forests can mitigate warming and ecological degradation of agricultural headwater streams | 9 |
11 |
12 |
15 |
9 |
16 |
1 |
6 |
1 |
10 |
34 |
1 |
125 |
| Rising methane emissions from boreal lakes due to increasing ice-free days | 6 |
3 |
21 |
24 |
29 |
8 |
1 |
3 |
5 |
1 |
3 |
9 |
113 |
| Risk assessment of gypsum amendment on agricultural fields : Effects of sulfate on riverine biota | 7 |
14 |
19 |
11 |
16 |
12 |
3 |
3 |
4 |
3 |
3 |
4 |
99 |
| Risks of producing and using indicators of sustainable development goals | 5 |
3 |
8 |
8 |
5 |
12 |
3 |
4 |
2 |
1 |
2 |
3 |
56 |
| River ice cover influence on sediment transportation at present and under projected hydroclimatic conditions | 8 |
9 |
15 |
33 |
41 |
31 |
1 |
0 |
1 |
2 |
3 |
2 |
146 |
| Russian dolls and Chinese whispers : Two perspectives on the unintended effects of sustainability indicator communication | 4 |
7 |
2 |
1 |
7 |
1 |
1 |
0 |
1 |
1 |
0 |
0 |
25 |
| Saliency-Based Multilabel Linear Discriminant Analysis | 13 |
3 |
12 |
8 |
9 |
5 |
2 |
3 |
0 |
0 |
0 |
3 |
58 |
| Same same, but different : The response of diatoms to environmental gradients in Fennoscandian streams and lakes – barcodes, traits and microscope data compared | 2 |
3 |
11 |
3 |
5 |
9 |
0 |
4 |
2 |
2 |
2 |
1 |
44 |
| Sampling effort and information quality provided by rare and common species in estimating assemblage structure | 14 |
8 |
12 |
14 |
16 |
12 |
12 |
3 |
5 |
3 |
2 |
7 |
108 |
| Saproxylic beetle assemblages in recently dead Scots pines : How traits modulate species' response to forest management? | 2 |
3 |
6 |
3 |
6 |
9 |
0 |
5 |
1 |
2 |
0 |
2 |
39 |
| Saturated Hydraulic Conductivity in Northern Peats Inferred From Other Measurements | 11 |
8 |
7 |
7 |
2 |
4 |
2 |
3 |
3 |
0 |
1 |
6 |
54 |
| Scientific models in legal judgements : The relationship between law and environmental science as problem-feeding | 4 |
11 |
1 |
1 |
5 |
8 |
0 |
0 |
1 |
0 |
0 |
0 |
31 |
| Sea-ice algal phenology in a warmer Arctic | 11 |
9 |
5 |
6 |
2 |
9 |
1 |
0 |
1 |
0 |
0 |
0 |
44 |
| Sea-Ice Bacteria Halomonas sp. Strain 363 and Paracoccus sp. Strain 392 Produce Multiple Types of Poly-3-Hydroxyalkaonoic Acid (PHA) Storage Polymers at Low Temperature | 8 |
4 |
6 |
1 |
8 |
8 |
4 |
4 |
6 |
2 |
2 |
9 |
62 |
| Seafloor sediments as microplastic sinks in the northern Baltic Sea : Negligible upward transport of buried microplastics by bioturbation | 3 |
2 |
11 |
4 |
5 |
7 |
1 |
1 |
2 |
2 |
0 |
3 |
41 |
| Seasonal and interannual dissolved organic carbon transport process dynamics in a subarctic headwater catchment revealed by high-resolution measurements | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Seasonal ecophysiology of Fucus vesiculosus (Phaeophyceae) in the Northern Baltic Sea | 14 |
9 |
15 |
6 |
8 |
7 |
7 |
6 |
4 |
3 |
2 |
5 |
86 |
| Seasonal variation in estuarine phytoplankton viability and its relationship with carbon dynamics in the Baltic Sea | 4 |
4 |
8 |
5 |
4 |
8 |
1 |
2 |
1 |
1 |
3 |
1 |
42 |
| Seasonal variation in the metacommunity structure of benthic macroinvertebrates in a large river-connected floodplain lake | 4 |
7 |
14 |
4 |
7 |
11 |
2 |
5 |
1 |
1 |
1 |
1 |
58 |
| Seasonality in recreation supply and demand in an urban lake ecosystem in Finland | 4 |
5 |
10 |
8 |
14 |
13 |
3 |
2 |
2 |
1 |
1 |
3 |
66 |
| Second homes during corona - safe or unsafe haven and for whom? Reflections from researchers around the world | 2 |
2 |
5 |
3 |
4 |
3 |
0 |
0 |
1 |
3 |
0 |
0 |
23 |
| Sectoral policies cause incoherence in forest management and ecosystem service provisioning | 2 |
4 |
13 |
4 |
13 |
16 |
2 |
1 |
2 |
1 |
4 |
2 |
64 |
| Sedimenttien haitallisten ympäristövaikutusten hallinta | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
1 |
5 |
| Severe drought in Finland : Modeling effects on water resources and assessing climate change impacts | 6 |
6 |
6 |
6 |
8 |
9 |
5 |
4 |
1 |
4 |
1 |
2 |
58 |
| Shallow-water mining undermines global sustainability goals | 10 |
4 |
13 |
4 |
4 |
7 |
4 |
0 |
1 |
0 |
1 |
1 |
49 |
| Shared socioeconomic pathways for climate change research in Finland : co-developing extended SSP narratives for agriculture | 4 |
5 |
14 |
6 |
4 |
9 |
3 |
2 |
2 |
3 |
0 |
0 |
52 |
| Shifting stoichiometry : Long‐term trends in stream‐dissolved organic matter reveal altered C:N ratios due to history of atmospheric acid deposition | 1 |
5 |
3 |
4 |
5 |
7 |
0 |
1 |
0 |
0 |
0 |
2 |
28 |
| Signals of potential species associations offer clues about community organisation of stream fish across seasons | 10 |
4 |
9 |
3 |
9 |
7 |
1 |
3 |
1 |
0 |
1 |
0 |
48 |
| Similar temperature sensitivity of soil mineral-associated organic carbon regardless of age | 16 |
10 |
15 |
12 |
20 |
19 |
17 |
7 |
2 |
4 |
11 |
3 |
136 |
| Simulating discharge in a non-dammed river of Southeastern South America using SWAT model | 4 |
4 |
8 |
4 |
9 |
8 |
2 |
3 |
3 |
0 |
0 |
1 |
46 |
| Simulation of organics in the atmosphere : evaluation of EMACv2.54 with the Mainz Organic Mechanism (MOM) coupled to the ORACLE (v1.0) submodel | 7 |
3 |
7 |
1 |
4 |
5 |
1 |
0 |
2 |
0 |
1 |
3 |
34 |
| Simultaneous allergic traits in dogs and their owners are associated with living environment, lifestyle and microbial exposures | 16 |
5 |
10 |
3 |
15 |
14 |
1 |
1 |
1 |
0 |
0 |
0 |
66 |
| Sisävesisedimenttien pilaantuneisuuden arviointi ja kunnostusvastuut | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
5 |
0 |
2 |
2 |
9 |
| Small wins enhancing sustainability transformations : Sustainable development policy in Finland | 3 |
4 |
8 |
7 |
8 |
6 |
0 |
2 |
1 |
0 |
3 |
2 |
44 |
| Small wins enhancing sustainability transformations : Sustainable development policy in Finland | 8 |
13 |
11 |
5 |
14 |
12 |
4 |
2 |
1 |
1 |
2 |
3 |
76 |
| Smartphone‐based estimation of green cover depends on the camera used | 6 |
18 |
9 |
2 |
3 |
24 |
1 |
1 |
0 |
0 |
0 |
1 |
65 |
| Social capital and governance : a social network analysis of forest biodiversity collaboration in Central Finland | 29 |
19 |
26 |
27 |
18 |
22 |
2 |
0 |
0 |
0 |
0 |
3 |
146 |
| Social impacts of biodiversity offsetting : A review | 6 |
6 |
6 |
5 |
9 |
10 |
0 |
0 |
3 |
0 |
0 |
0 |
45 |
| Socio-economic factors boosting the effectiveness of marine protected areas: A Bayesian network analysis | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Soiden eliölajit ja niiden uhanalaisuus | 8 |
1 |
9 |
10 |
14 |
5 |
3 |
9 |
11 |
8 |
12 |
12 |
102 |
| Soiden kasvillisuus | 7 |
12 |
12 |
10 |
3 |
9 |
5 |
15 |
9 |
13 |
16 |
11 |
122 |
| Soidensuojelun täydennysehdotus ottaa huomioon suoluonnon monimuotoisuuden | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
4 |
2 |
4 |
2 |
4 |
16 |
| Sources and sinks of greenhouse gases in the landscape: Approach for spatially explicit estimates | 12 |
6 |
13 |
3 |
5 |
16 |
4 |
1 |
3 |
6 |
4 |
3 |
76 |
| Sowing and Harvesting Measures to Cope with Challenges of Cover Crops Experienced by Finnish Farmers | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
76 |
2 |
1 |
79 |
| Spatial and temporal ecological uniqueness of Andean diatom communities are correlated with climate, geodiversity and long-term limnological change | 3 |
3 |
4 |
4 |
8 |
8 |
0 |
0 |
1 |
0 |
1 |
1 |
33 |
| Spatial and temporal variability of ambient underwater sound in the Baltic Sea | 8 |
4 |
6 |
6 |
5 |
4 |
4 |
1 |
0 |
0 |
1 |
0 |
39 |
| Spatial and temporal wave climate variability along the south coast of Sweden during 1959–2021 | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
2 |
4 |
9 |
| Spatial distribution of residential wood combustion emissions in the Nordic countries : How well national inventories represent local emissions? | 3 |
7 |
12 |
6 |
5 |
9 |
1 |
1 |
0 |
0 |
1 |
3 |
48 |
| Spatial prioritization for urban Biodiversity Quality using biotope maps and expert opinion | 2 |
5 |
7 |
0 |
4 |
18 |
5 |
2 |
1 |
3 |
3 |
0 |
50 |
| Spatial synchrony is related to environmental change in Finnish moth communities | 5 |
2 |
5 |
5 |
12 |
10 |
1 |
0 |
1 |
0 |
1 |
1 |
43 |
| Spatial variation of flow characteristics in a subarctic meandering river in ice-covered and open-channel conditions : A 2D hydrodynamic modelling approach | 8 |
3 |
11 |
8 |
5 |
4 |
0 |
2 |
2 |
2 |
2 |
0 |
47 |
| Spatio-temporal population dynamics of six phytoplankton taxa | 5 |
7 |
5 |
5 |
6 |
7 |
0 |
4 |
0 |
1 |
3 |
4 |
47 |
| Spatiotemporal analysis of lake chlorophyll-a with combined in situ and satellite data | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
5 |
2 |
7 |
| Spatiotemporal management of solar, wind and hydropower across continental Europe | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Spatiotemporal variability and diffusive emissions of greenhouse gas in a shallow eutrophic lake in Inner Mongolia, China | 20 |
12 |
11 |
2 |
6 |
8 |
2 |
1 |
0 |
1 |
2 |
2 |
67 |
| Species–environment relationships of fish and map‐based variables in small boreal streams : Linkages with climate change and bioassessment | 8 |
5 |
7 |
11 |
10 |
7 |
0 |
0 |
0 |
1 |
1 |
0 |
50 |
| Speed-up and multi-view extensions to subclass discriminant analysis | 2 |
5 |
7 |
11 |
5 |
7 |
1 |
2 |
0 |
0 |
1 |
1 |
42 |
| Stakeholders engagement for solving mobility problems in touristic remote areas from the Baltic Sea Region | 8 |
3 |
13 |
6 |
5 |
10 |
4 |
3 |
3 |
1 |
1 |
1 |
58 |
| Status and trends in the rate of introduction of marine non-indigenous species in European seas | 12 |
9 |
8 |
5 |
6 |
9 |
3 |
3 |
1 |
1 |
1 |
2 |
60 |
| Steering household consumption with carbon footprint data : a critical assessment | 43 |
42 |
44 |
45 |
47 |
39 |
20 |
6 |
10 |
0 |
5 |
8 |
309 |
| Stochastic processes and ecological connectivity drive stream invertebrate community responses to short‐term drought | 3 |
4 |
9 |
14 |
11 |
10 |
0 |
0 |
1 |
0 |
0 |
0 |
52 |
| Stochasticity overrides deterministic processes in structuring macroinvertebrate communities in a plateau aquatic system | 4 |
4 |
11 |
7 |
5 |
6 |
1 |
0 |
2 |
1 |
1 |
0 |
42 |
| Storylines nailing or failing sustainability : Energy, mining and mobility as narrative arenas for societal transition | 0 |
0 |
0 |
0 |
36 |
14 |
0 |
4 |
2 |
2 |
2 |
1 |
61 |
| Strategy towards producing relevant and reliable data for the hazard assessment of micro- and nanoplastics in agricultural soils | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Stream bryophyte recovery after extreme flood disturbance takes several years | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Stream dissolved organic matter in permafrost regions shows surprising compositional similarities but negative priming and nutrient effects | 6 |
11 |
19 |
4 |
6 |
14 |
3 |
3 |
0 |
0 |
0 |
0 |
66 |
| Strengthening the policy framework to resolve lax implementation of the Baltic Sea Action Plan for agriculture | 5 |
4 |
9 |
4 |
9 |
8 |
2 |
2 |
0 |
2 |
1 |
5 |
51 |
| Studies in Basidiodendron eyrei and similar-looking taxa (Auriculariales, Basidiomycota) | 6 |
7 |
10 |
7 |
9 |
19 |
4 |
3 |
6 |
14 |
19 |
8 |
112 |
| Studies in the Basidiodendron caesiocinereum complex (Auriculariales, Basidiomycota) | 3 |
4 |
12 |
3 |
6 |
14 |
4 |
5 |
5 |
1 |
0 |
4 |
61 |
| Study protocol of the European Urban Burden of Disease Project : a health impact assessment study | 5 |
4 |
9 |
8 |
6 |
7 |
1 |
3 |
0 |
0 |
0 |
0 |
43 |
| Substances of emerging concern in Baltic Sea water : Review on methodological advances for the environmental assessment and proposal for future monitoring | 7 |
8 |
8 |
4 |
4 |
9 |
2 |
2 |
3 |
1 |
2 |
1 |
51 |
| Substitution impacts of Nordic wood-based multi-story building types : influence of the decarbonization of the energy sector and increased recycling of construction materials | 7 |
7 |
15 |
6 |
7 |
8 |
3 |
2 |
2 |
1 |
4 |
1 |
63 |
| Substitution impacts of wood‐based textile fibers : Influence of market assumptions | 7 |
8 |
11 |
8 |
7 |
8 |
2 |
6 |
3 |
3 |
6 |
2 |
71 |
| Substrate limitation of a habitat-forming genus Fucus under different water clarity scenarios in the northern Baltic Sea | 12 |
4 |
7 |
2 |
4 |
6 |
0 |
2 |
3 |
0 |
1 |
0 |
41 |
| Successful growth of coastal marine microalgae in wastewater from a salmon recirculating aquaculture system | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Suoluonnon tutkimista suomalais-venäläisenä yhteistyönä | 1 |
1 |
4 |
6 |
6 |
4 |
5 |
5 |
2 |
0 |
6 |
5 |
45 |
| Suoluontotyyppien uhanalaisuus | 5 |
15 |
11 |
16 |
12 |
10 |
1 |
2 |
6 |
4 |
6 |
1 |
89 |
| Surprise, surprise — a flying squirrel! Learning to protect the unexpected | 6 |
7 |
9 |
4 |
4 |
10 |
1 |
1 |
2 |
1 |
5 |
0 |
50 |
| Sustainability assessment of technologies for resource recovery in two Baltic Sea Region case-studies using multi-criteria analysis | 4 |
2 |
8 |
3 |
4 |
5 |
5 |
1 |
2 |
1 |
1 |
1 |
37 |
| Sustainable lake restoration: From challenges to solutions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Synthesis of habitat restoration impacts on young-of-the-year salmonids in boreal rivers | 12 |
5 |
4 |
4 |
3 |
6 |
2 |
0 |
0 |
0 |
0 |
0 |
36 |
| Syyt ympäristölupahakemusten pitkiin käsittelyaikoihin aluehallintovirastoissa | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
6 |
4 |
4 |
4 |
1 |
19 |
| Targeting net climate benefits by wood utilization in Finland : Participatory backcasting combined with quantitative scenario exploration | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
0 |
1 |
2 |
| Taxonomic, functional, and phylogenetic beta diversity patterns of stream fish assemblages in tropical agroecosystems | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Technical and social knowledge discontinuities in the multi-objective management of private forests in Finland | 9 |
3 |
8 |
0 |
9 |
7 |
2 |
0 |
2 |
1 |
1 |
2 |
44 |
| Technology Readiness Level of biodiversity monitoring with molecular methods – where are we on the road to routine implementation? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Telecouplings in Atlantic cod—The role of global trade and climate change | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
3 |
3 |
3 |
9 |
| Temperature and spatial connectivity drive patterns in freshwater macroinvertebrate diversity across the Arctic | 3 |
4 |
8 |
9 |
10 |
12 |
2 |
1 |
1 |
9 |
2 |
1 |
62 |
| Temporal patterns of phytoplankton phenology across high latitude lakes unveiled by long-term time series of satellite data | 5 |
8 |
9 |
4 |
8 |
7 |
4 |
0 |
3 |
3 |
1 |
1 |
53 |
| Temporal understanding of the Water–Energy Nexus : A literature review | 7 |
5 |
14 |
7 |
8 |
10 |
1 |
5 |
2 |
2 |
3 |
3 |
67 |
| Testing citizen science as a tool for monitoring surface water microplastics | 5 |
4 |
15 |
1 |
9 |
7 |
2 |
3 |
3 |
1 |
17 |
2 |
69 |
| The activity and functions of soil microbial communities in the Finnish sub-Arctic vary across vegetation types | 13 |
5 |
10 |
6 |
9 |
9 |
5 |
4 |
3 |
3 |
0 |
1 |
68 |
| The Baltic Health Index (BHI) : Assessing the social–ecological status of the Baltic Sea | 0 |
7 |
7 |
15 |
12 |
16 |
1 |
1 |
1 |
0 |
0 |
1 |
61 |
| The challenge of combining variable retention and prescribed burning in Finland | 7 |
6 |
7 |
6 |
9 |
15 |
2 |
1 |
3 |
13 |
9 |
1 |
79 |
| The challenging paths to net-zero emissions : insights from the monitoring of national policy mixes | 5 |
3 |
8 |
8 |
13 |
9 |
6 |
5 |
3 |
3 |
0 |
1 |
64 |
| The co-evolution of policy realities and environmental liabilities : Analysing the ontological work of policy documents | 3 |
5 |
3 |
1 |
5 |
3 |
0 |
1 |
0 |
0 |
0 |
1 |
22 |
| The dangerous transporters : a study of microplastic-associated bacteria passing through municipal wastewater treatment | 16 |
26 |
34 |
11 |
11 |
10 |
7 |
3 |
2 |
77 |
15 |
15 |
227 |
| The drivers of intra‐ and interregional labor mobility over the industry life cycle of the high‐tech sector | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| The economic cost of hydropower environmental constraints under decreasing price volatility | 16 |
11 |
12 |
8 |
10 |
13 |
5 |
2 |
2 |
2 |
1 |
6 |
88 |
| The economic costs, management and regulation of biological invasions in the Nordic countries | 17 |
23 |
21 |
15 |
22 |
7 |
3 |
3 |
3 |
5 |
4 |
3 |
126 |
| The effect of information nudges on energy saving : Observations from a randomized field experiment in Finland | 10 |
10 |
17 |
8 |
11 |
16 |
1 |
4 |
0 |
1 |
1 |
1 |
80 |
| The effect of urbanization on freshwater macroinvertebrates : Knowledge gaps and future research directions | 6 |
9 |
9 |
7 |
11 |
9 |
1 |
5 |
1 |
3 |
1 |
2 |
64 |
| The eLTER research infrastructure: Current design and coverage of environmental and socio-ecological gradients | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| The EU Horizon 2020 project GRACE : integrated oil spill response actions and environmental effects | 11 |
8 |
7 |
4 |
7 |
7 |
1 |
4 |
1 |
2 |
0 |
0 |
52 |
| The Finnish Biodiversity Information Facility as a best-practice model for biodiversity data infrastructures | 9 |
3 |
6 |
6 |
10 |
5 |
3 |
3 |
0 |
0 |
4 |
3 |
52 |
| The future in sustainability transitions - Interlinkages between the multi-level perspective and futures studies | 15 |
21 |
38 |
30 |
15 |
19 |
1 |
3 |
8 |
7 |
12 |
4 |
173 |
| The future of DNA barcoding : reflections from early career researchers | 5 |
8 |
7 |
8 |
9 |
6 |
2 |
3 |
3 |
1 |
4 |
2 |
58 |
| The impact of measures to reduce ambient air PM10 concentrations originating from road dust, evaluated for a street canyon in Helsinki | 9 |
5 |
9 |
4 |
2 |
8 |
0 |
1 |
1 |
1 |
0 |
2 |
42 |
| The impacts of dietary change in Finland : food system approach | 5 |
5 |
9 |
11 |
12 |
14 |
6 |
25 |
3 |
2 |
5 |
6 |
103 |
| The influence of residential wood combustion on the concentrations of PM2.5 in four Nordic cities | 2 |
4 |
9 |
4 |
12 |
10 |
29 |
3 |
2 |
3 |
3 |
3 |
84 |
| The limits of spatial data? Sense-making within the development and different uses of Finnish urban-rural classification | 14 |
13 |
11 |
8 |
14 |
10 |
4 |
3 |
3 |
3 |
6 |
2 |
91 |
| The occurrence, distribution, and risks of PFAS at AFFF-impacted sites in Finland | 8 |
19 |
20 |
18 |
20 |
24 |
7 |
12 |
6 |
14 |
28 |
10 |
186 |
| The orchestration of sustainable mobility service innovations : understanding the manifold agency of car sharing operators | 10 |
6 |
15 |
4 |
6 |
12 |
1 |
1 |
0 |
1 |
0 |
0 |
56 |
| The politics of national SDG indicator systems: A comparison of four European countries | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
9 |
1 |
3 |
13 |
| The potential for evolutionary rescue in an Arctic seashore plant threatened by climate change | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| The quest for seafloor macrolitter : a critical review of background knowledge, current methods and future prospects | 8 |
5 |
10 |
1 |
5 |
13 |
2 |
3 |
1 |
2 |
0 |
2 |
52 |
| The role of environmental conditions, climatic factors and spatial processes in driving multiple facets of stream macroinvertebrate beta diversity in a climatically heterogeneous mountain region | 1 |
2 |
8 |
7 |
7 |
9 |
1 |
2 |
4 |
2 |
3 |
1 |
47 |
| The Role of Food Web Interactions in Multispecies Fisheries Management : Bio-economic Analysis of Salmon, Herring and Grey Seal in the Northern Baltic Sea | 4 |
2 |
8 |
5 |
10 |
20 |
5 |
4 |
1 |
2 |
2 |
0 |
63 |
| The role of indicators in improving timeliness of international environmental reports | 3 |
5 |
1 |
0 |
6 |
3 |
0 |
1 |
0 |
0 |
0 |
0 |
19 |
| The role of MSC Marine Certification in fisheries governance in Finland | 9 |
2 |
7 |
18 |
11 |
16 |
4 |
1 |
1 |
0 |
7 |
0 |
76 |
| The smart meets the conventional : Media storylines and societal frames on the energy action of housing cooperatives | 9 |
10 |
9 |
12 |
8 |
9 |
1 |
4 |
3 |
0 |
0 |
1 |
66 |
| The spectral species concept in living color | 15 |
8 |
11 |
6 |
9 |
8 |
0 |
1 |
0 |
0 |
1 |
1 |
60 |
| The three Rs of river ecosystem resilience : Resources, recruitment, and refugia | 19 |
14 |
19 |
24 |
19 |
24 |
5 |
1 |
3 |
0 |
1 |
1 |
130 |
| The unknown known – A review of local ecological knowledge in relation to forest biodiversity conservation | 18 |
24 |
34 |
25 |
43 |
20 |
1 |
1 |
0 |
1 |
3 |
2 |
172 |
| The urban density in two Nordic capitals – comparing the development of Oslo and Helsinki metropolitan regions | 2 |
8 |
10 |
7 |
9 |
5 |
2 |
2 |
3 |
7 |
5 |
0 |
60 |
| The urgency of Arctic change | 13 |
13 |
15 |
9 |
11 |
13 |
0 |
3 |
1 |
3 |
2 |
10 |
93 |
| The Use of Ribosomal RNA as a Microbial Source Tracking Target Highlights the Assay Host-Specificity Requirement in Water Quality Assessments | 3 |
5 |
12 |
7 |
7 |
15 |
4 |
0 |
0 |
1 |
5 |
2 |
61 |
| The value of perfect and imperfect information in lake monitoring and management | 7 |
2 |
10 |
5 |
7 |
10 |
4 |
1 |
3 |
2 |
2 |
1 |
54 |
| Thermostat or thermometer? A Finnish perspective on the overloaded role of sustainability indicators in societal transition | 4 |
1 |
4 |
6 |
7 |
5 |
0 |
2 |
1 |
1 |
2 |
1 |
34 |
| Time series of freshwater macroinvertebrate abundances and site characteristics of European streams and river | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Tissue-specific study across the stem reveals the chemistry and transcriptome dynamics of birch bark. | 3 |
14 |
12 |
13 |
23 |
17 |
4 |
4 |
2 |
4 |
3 |
4 |
103 |
| To separate or not? A comparison of wastewater management systems for the new city district of Hiedanranta, Finland | 4 |
4 |
11 |
7 |
7 |
8 |
2 |
1 |
0 |
0 |
4 |
0 |
48 |
| Too big to succeed? Institutional inertia in low-carbon district heating experiment | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
7 |
2 |
6 |
15 |
| Too important to fail? : Evaluating legal adaptive capacity for increasing coastal and marine aquaculture production in EU-Finland | 4 |
2 |
10 |
1 |
5 |
8 |
0 |
3 |
2 |
2 |
1 |
2 |
40 |
| Toward a European coastal observing network to provide better answers to science and to societal challenges : The JERICO research infrastructure | 7 |
1 |
7 |
3 |
1 |
6 |
3 |
0 |
1 |
0 |
1 |
0 |
30 |
| Toward phytoplankton parasite detection using autoencoders | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
6 |
2 |
6 |
14 |
| Towards a Low-Carbon Plastic Waste Recycling in Finland: Evaluating the Impacts of Improvement Measures on GHG Emissions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Towards agricultural soil carbon monitoring, reporting, and verification through the Field Observatory Network (FiON) | 16 |
6 |
11 |
10 |
17 |
27 |
1 |
0 |
0 |
0 |
0 |
3 |
91 |
| Towards agricultural soil carbon monitoring, reporting, and verification through the Field Observatory Network (FiON) | 5 |
7 |
21 |
8 |
7 |
21 |
2 |
6 |
2 |
3 |
3 |
1 |
86 |
| Towards critical white ice conditions in lakes under global warming | 5 |
5 |
11 |
9 |
6 |
5 |
1 |
3 |
0 |
0 |
0 |
0 |
45 |
| Towards efficient and reliable utilization of automated data collection: Media scrapers applied to news on climate change | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Towards linking freshwater plants and ecosystems via functional biogeography | 4 |
2 |
2 |
7 |
9 |
2 |
0 |
0 |
1 |
1 |
1 |
1 |
30 |
| Towards operational phytoplankton recognition with automated high-throughput imaging, near-real-time data processing, and convolutional neural networks | 21 |
30 |
26 |
15 |
20 |
21 |
8 |
9 |
5 |
4 |
5 |
3 |
167 |
| Towards sustainable mobility – Transformative scenarios for 2034 | 13 |
7 |
19 |
16 |
24 |
15 |
11 |
6 |
4 |
2 |
3 |
4 |
124 |
| Towards sustainable urban transport—Political agenda formation and policy windows in Helsinki, Oslo, and Stockholm | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Trait response of three Baltic Sea spring dinoflagellates to temperature, salinity, and light gradients | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
10 |
4 |
4 |
18 |
| Transcending sectoral boundaries? Discovering built-environment indicators through knowledge co-production for enhanced planning for well-being in Finnish cities | 3 |
6 |
7 |
6 |
6 |
10 |
36 |
3 |
0 |
8 |
3 |
1 |
89 |
| Transformative change needs direction | 0 |
0 |
0 |
0 |
16 |
30 |
2 |
1 |
3 |
0 |
2 |
1 |
55 |
| Transformative governance: Exploring theory of change and the role of the law | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Transformative outcomes : assessing and reorienting experimentation with transformative innovation policy | 12 |
5 |
8 |
11 |
16 |
17 |
6 |
2 |
2 |
1 |
0 |
1 |
81 |
| Transforming innovation policy in the context of global security | 5 |
5 |
13 |
5 |
8 |
10 |
0 |
2 |
0 |
3 |
0 |
2 |
53 |
| Transition governance for energy efficiency - insights from a systematic review of Swedish policy evaluation practices | 6 |
11 |
10 |
2 |
4 |
6 |
5 |
3 |
1 |
5 |
3 |
6 |
62 |
| Transition pathway for the city toward low-emission district heating system with heat auctions promoting third-party network access | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Transitions in planning : transformative policy visions of the circular economy and blue bioeconomy meet planning practice | 13 |
4 |
10 |
10 |
7 |
13 |
2 |
2 |
3 |
1 |
1 |
3 |
69 |
| Transport dynamics in a complex coastal archipelago | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Tree species classification from airborne hyperspectral and LiDAR data using 3D convolutional neural networks | 16 |
16 |
36 |
35 |
31 |
26 |
9 |
12 |
14 |
16 |
14 |
4 |
229 |
| Tulevaisuuden kaupunki on käveltävä – globaaleja mittareita kaupunkiseutuja kirittämään | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
12 |
27 |
8 |
47 |
| Two sides of biogas: Review of ten dichotomous argumentation lines of sustainable energy systems | 1 |
12 |
14 |
6 |
9 |
13 |
8 |
3 |
6 |
5 |
6 |
5 |
88 |
| Two-stage channels can enhance local biodiversity in agricultural landscapes | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Unawareness in environmental protection : The case of light pollution from traffic | 11 |
36 |
16 |
4 |
12 |
16 |
1 |
1 |
3 |
3 |
2 |
0 |
105 |
| Understanding circular economy in everyday life : Perceptions of young adults in the Finnish context | 35 |
27 |
48 |
37 |
31 |
38 |
9 |
6 |
13 |
8 |
23 |
18 |
293 |
| Understanding macroinvertebrate metacommunity organization using a nested study design across a mountainous river network | 4 |
1 |
6 |
3 |
3 |
5 |
0 |
1 |
0 |
1 |
1 |
0 |
25 |
| Understanding the role of biodiversity in the climate, food, water, energy, transport and health nexus in Europe | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Underwater acoustic environment of coastal sea with heavy shipping traffic : NE Baltic Sea during wintertime implementation | 9 |
3 |
2 |
4 |
6 |
4 |
0 |
0 |
3 |
0 |
0 |
3 |
34 |
| Undrained peatland areas disturbed by surrounding drainage : A large scale GIS analysis in Finland with a special focus on aapa mires | 22 |
14 |
23 |
11 |
5 |
13 |
9 |
3 |
5 |
5 |
5 |
2 |
117 |
| Unmanned Aircraft System (UAS) Structure-From-Motion (SfM) for monitoring the changed flow paths and wetness in minerotrophic peatland restoration | 10 |
4 |
14 |
8 |
7 |
10 |
2 |
1 |
0 |
0 |
0 |
0 |
56 |
| Unobserved preferences and dynamic platform pricing under positive network externality | 8 |
1 |
10 |
5 |
6 |
7 |
3 |
0 |
2 |
2 |
1 |
1 |
46 |
| Unrecognized, concealed, or forgotten – the case of absent information in risk communication | 2 |
3 |
1 |
1 |
6 |
4 |
1 |
0 |
2 |
0 |
0 |
0 |
20 |
| Untangling the interactions of sustainability targets : synergies and trade-offs in the Northern European context | 1 |
1 |
6 |
5 |
4 |
11 |
1 |
0 |
0 |
0 |
1 |
5 |
35 |
| Upwelled plankton community modulates surface bloom succession and nutrient availability in a natural plankton assemblage | 0 |
0 |
0 |
0 |
16 |
10 |
3 |
2 |
1 |
0 |
0 |
0 |
32 |
| Urban sustainability and the SDGs : A Nordic perspective and opportunity for integration | 9 |
5 |
13 |
7 |
10 |
9 |
4 |
4 |
1 |
1 |
3 |
1 |
67 |
| Urbanization extends flight phenology and leads to local adaptation of seasonal plasticity in Lepidoptera | 5 |
2 |
5 |
4 |
5 |
8 |
1 |
0 |
3 |
1 |
0 |
3 |
37 |
| Urine : The potential, value chain and its sustainable management | 5 |
1 |
4 |
3 |
7 |
9 |
4 |
1 |
1 |
0 |
0 |
0 |
35 |
| Using energy vulnerability framework to understand household agency in sustainability transitions: Experiences from Canada and Finland | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Using functional traits and phylogeny to understand local extinction risk in dragonflies and damselflies (Odonata) | 5 |
3 |
8 |
4 |
8 |
9 |
0 |
0 |
1 |
0 |
1 |
1 |
40 |
| Using impact response surfaces to analyse the likelihood of impacts on crop yield under probabilistic climate change | 9 |
4 |
6 |
11 |
4 |
9 |
0 |
3 |
7 |
5 |
2 |
4 |
64 |
| Using traits to explain interspecific variation in diatom occupancy and abundance across lakes and streams | 9 |
7 |
12 |
10 |
9 |
13 |
0 |
5 |
3 |
3 |
1 |
3 |
75 |
| Utilizing the flexibility of distributed thermal storage in solar power forecast error cost minimization | 5 |
8 |
11 |
6 |
7 |
12 |
4 |
2 |
6 |
2 |
1 |
0 |
64 |
| Validation of an imaging FTIR spectroscopic method for analyzing microplastics ingestion by Finnish lake fish (Perca fluviatilis and Coregonus albula) | 9 |
6 |
13 |
13 |
12 |
4 |
1 |
0 |
3 |
2 |
0 |
2 |
65 |
| Valuation through deliberation - Citizens' panels on peatland ecosystem services in Finland | 1 |
3 |
11 |
5 |
6 |
9 |
0 |
2 |
0 |
2 |
0 |
0 |
39 |
| Value of Spatially Distributed Rainfall Design Events—Creating Basin-Scale Stochastic Design Storm Ensembles | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
11 |
4 |
4 |
19 |
| Variation in the fatty acid profiles of two cold water diatoms grown under different temperature, light, and nutrient regimes | 2 |
2 |
4 |
4 |
8 |
8 |
0 |
2 |
0 |
2 |
2 |
0 |
34 |
| Vedenalaisen melun rajoittaminen | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Viability of pico- and nanophytoplankton in the Baltic Sea during spring | 2 |
2 |
7 |
5 |
6 |
9 |
0 |
2 |
3 |
1 |
0 |
2 |
39 |
| Viheralueiden elonkirjo : asiantuntijakysely ja luonnon monimuotoisuuden laatumittaristo kaupunkisuunnittelun tueksi | 0 |
0 |
0 |
23 |
16 |
12 |
5 |
1 |
2 |
3 |
6 |
0 |
68 |
| Virus-host interactions and genetic diversity of Antarctic Sea Ice bacteriophages | 10 |
14 |
9 |
12 |
9 |
7 |
1 |
1 |
1 |
2 |
1 |
1 |
68 |
| Voices for the darkness: online survey on public perceptions on light pollution as an environmental problem | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Voluntary agreements to protect private forests – A realist review | 11 |
0 |
7 |
3 |
13 |
9 |
6 |
6 |
1 |
8 |
6 |
4 |
74 |
| Voluntary participation for sustainability transition : experiences from the 'Commitment to Sustainable Development 2050' | 15 |
5 |
2 |
9 |
5 |
3 |
0 |
1 |
0 |
0 |
0 |
1 |
41 |
| Water accounting as a tool for tracing the industries responsible for the point-source loads into water bodies | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
6 |
4 |
3 |
13 |
| Water-smart circular economy – Conceptualisation, transitional policy instruments and stakeholder perception | 11 |
4 |
10 |
3 |
17 |
13 |
2 |
1 |
1 |
1 |
1 |
1 |
65 |
| Wave stress and biotic facilitation drive community composition in a marginal hard-bottom ecosystem | 7 |
3 |
9 |
1 |
7 |
8 |
1 |
5 |
6 |
1 |
1 |
4 |
53 |
| Weight-based pay-as-you-throw pricing model : Encouraging sorting in households through waste fees | 22 |
16 |
36 |
35 |
30 |
16 |
3 |
0 |
6 |
0 |
4 |
0 |
168 |
| What about citizens? A literature review of citizen engagement in sustainability transitions research | 22 |
18 |
38 |
35 |
36 |
35 |
13 |
3 |
12 |
6 |
7 |
6 |
231 |
| What conditions favor the influence of seasonally frozen ground on hydrological partitioning? : a systematic review | 10 |
12 |
14 |
9 |
11 |
8 |
1 |
3 |
2 |
0 |
3 |
3 |
76 |
| What conditions favor the influence of seasonally frozen ground on hydrological partitioning? A systematic review | 7 |
7 |
10 |
6 |
11 |
5 |
0 |
1 |
1 |
1 |
0 |
1 |
50 |
| What does it take to study learning in transitions? A case of citizen energy in Finland | 12 |
9 |
19 |
7 |
12 |
5 |
5 |
5 |
2 |
2 |
0 |
1 |
79 |
| What Makes a Liveable Neighborhood? Role of Socio-Demographic, Dwelling, and Environmental Factors and Participation in Finnish Urban and Suburban Areas | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| What makes urban greenspace unique – relationships between citizens’ perceptions on unique urban nature, biodiversity and environmental factors | 14 |
30 |
25 |
27 |
18 |
18 |
5 |
4 |
5 |
4 |
20 |
19 |
189 |
| When and how can we predict adaptive responses to climate change? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| When the circular economy diverges : The co-evolution of biogas business models and material circuits in Finland | 6 |
8 |
8 |
7 |
15 |
11 |
4 |
0 |
4 |
0 |
2 |
2 |
67 |
| Widespread synchrony in phosphorus concentrations in northern lakes linked to winter temperature and summer precipitation | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
8 |
1 |
4 |
13 |
| Within‐field variation of crop yield loss from cover crops | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Wood substitution potential in greenhouse gas emission reduction - review on current state and application of displacement factors | 4 |
3 |
12 |
3 |
7 |
8 |
6 |
2 |
2 |
3 |
1 |
3 |
54 |
| Wood-decaying fungi in old-growth boreal forest fragments : extinctions and colonizations over 20 years | 3 |
0 |
6 |
1 |
2 |
5 |
1 |
0 |
1 |
1 |
0 |
2 |
22 |
| Wood-inhabiting fungal responses to forest naturalness vary among morpho-groups | 5 |
5 |
8 |
2 |
2 |
10 |
5 |
1 |
0 |
0 |
2 |
1 |
41 |
| Would turkeys vote for Christmas? New entrant strategies and coopetitive tensions in the emerging demand response industry | 1 |
5 |
7 |
2 |
3 |
6 |
0 |
0 |
0 |
1 |
1 |
0 |
26 |
| Yhdyskuntajätevesien satunnaispäästöjen ympäristö- ja terveysriskit | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Ympäristölle haitallisista tuista | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Ympäristöväittämistä ensimmäisen kerran perusteellista tietoa | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
5 |
1 |
1 |
7 |
| Zooplankton dilemma in the twilight (News & views) | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| ‘I don’t fertilise quite like that’ : Mediating and distancing capacities of nutrient records at Finnish farms | 3 |
8 |
4 |
2 |
4 |
4 |
3 |
2 |
0 |
2 |
0 |
0 |
32 |
| A strategy for successful integration of DNA-based methods in aquatic monitoring | 15 |
12 |
16 |
13 |
19 |
18 |
6 |
5 |
2 |
9 |
12 |
1 |
128 |
| Recommendations for the preservation of environmental samples in diatom metabarcoding studies | 1 |
2 |
10 |
5 |
8 |
10 |
4 |
3 |
0 |
0 |
1 |
1 |
45 |
| Review of the genus Plutothrix Förster, 1856 (Hymenoptera, Pteromalidae) with a key to Palaearctic species | 3 |
25 |
11 |
9 |
11 |
12 |
2 |
5 |
4 |
3 |
6 |
2 |
93 |