| The entire DSpace / Artikkelit / Artikkeleita tieteenaloittain / Luonnontieteiden artikkeleita | 7 / 2023 | 8 / 2023 | 9 / 2023 | 10 / 2023 | 11 / 2023 | 12 / 2023 | 1 / 2024 | 2 / 2024 | 3 / 2024 | 4 / 2024 | 5 / 2024 | 6 / 2024 | Total |
|---|
| A Case Study of the Effects of CO2-Induced Climatic Warming on Forest Growth and the Forest Sector : A. Productivity Reactions of Northern Boreal Forests. | 1 |
0 |
2 |
1 |
0 |
8 |
1 |
0 |
2 |
2 |
2 |
0 |
19 |
| A discrete time model for succession of ground cover communities after clear cutting. | 2 |
1 |
2 |
3 |
2 |
2 |
1 |
2 |
1 |
3 |
0 |
4 |
23 |
| A large carbon sink in the woody biomass of Northern forests | 4 |
4 |
7 |
2 |
1 |
3 |
5 |
1 |
2 |
3 |
2 |
2 |
36 |
| A method for estimating above-ground biomass in Phragmites stands | 2 |
3 |
2 |
120 |
1 |
0 |
1 |
3 |
2 |
1 |
1 |
2 |
138 |
| A Peptide Derived from the Intercellular Adhesion Molecule-2 Regulates the Avidity of the Leukocyte Integrins CD11b/CD18 and CDllc/CD18 | 0 |
0 |
3 |
0 |
1 |
0 |
1 |
2 |
0 |
1 |
0 |
0 |
8 |
| A simple local 3-approximation algorithm for vertex cover | 1 |
1 |
5 |
1 |
1 |
0 |
0 |
0 |
2 |
1 |
3 |
11 |
26 |
| A survey of the parasites from the Baltic Smelt, Osmerus Eperlanus | 4 |
1 |
2 |
4 |
3 |
1 |
0 |
1 |
1 |
1 |
2 |
2 |
22 |
| Abborre och flundra : två åländska läckerbitar | 1 |
0 |
1 |
1 |
4 |
2 |
1 |
3 |
0 |
1 |
1 |
0 |
15 |
| Accumulation of mercury in fish and man from reservoirs in Northern Finland | 1 |
7 |
5 |
3 |
1 |
5 |
0 |
2 |
1 |
2 |
4 |
2 |
33 |
| Acid rain in Europe : A framework to assist decision making. | 0 |
3 |
1 |
2 |
1 |
4 |
0 |
0 |
2 |
1 |
0 |
0 |
14 |
| Acidification in Europe : A Simulation Model for Evaluating Control Strategies | 1 |
3 |
3 |
3 |
2 |
2 |
12 |
1 |
5 |
0 |
1 |
4 |
37 |
| Acidification of forest soils : Model development and application for analyzing impacts of acidic deposition in Europe. | 3 |
4 |
1 |
2 |
2 |
1 |
7 |
1 |
2 |
3 |
2 |
0 |
28 |
| Adaptation to light fluctuations in the frog retina | 0 |
7 |
1 |
6 |
0 |
2 |
4 |
8 |
1 |
3 |
4 |
3 |
39 |
| Adaptation-related changes in the spatial and temporal summation of frog retinal ganglion cells | 0 |
0 |
0 |
2 |
1 |
3 |
3 |
7 |
1 |
4 |
3 |
0 |
24 |
| Adjustments of ejaculation rates in response to risk of sperm competition in a fish, the bitterling (Rhodeus sericeus) | 0 |
0 |
1 |
0 |
4 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
5 |
| An(other) Entropy-Bounded Compressed Suffix Tree | 4 |
2 |
4 |
4 |
6 |
2 |
2 |
0 |
1 |
1 |
0 |
0 |
26 |
| Anomalous isotopic effect on vibrational properties of HXeOH | 3 |
0 |
1 |
1 |
3 |
0 |
2 |
1 |
4 |
0 |
2 |
0 |
17 |
| Anteckningar om vattenkvaliteten och fiskfaunan vid Nåtö biologiska station i Lemlands skärgård på Åland | 2 |
2 |
2 |
3 |
2 |
1 |
0 |
0 |
0 |
0 |
2 |
1 |
15 |
| Application of coal ash to environmental improvement Transformation into zeolite, potassium fertilizer, and FGD absorbent | 8 |
11 |
8 |
6 |
7 |
3 |
3 |
3 |
6 |
12 |
2 |
4 |
73 |
| Arsenic in groundwater in the Bengal Delta Plain : slow poisoning in Bangladesh | 6 |
6 |
4 |
6 |
3 |
2 |
9 |
6 |
5 |
3 |
3 |
4 |
57 |
| Arvoituksellinen ankerias | 1 |
3 |
3 |
3 |
1 |
3 |
5 |
2 |
2 |
2 |
2 |
1 |
28 |
| Atmospheric Deposition of Sulfur, Nitrogen and basic Cations onto European Forests : Observations and Model Calculations | 0 |
3 |
2 |
1 |
4 |
0 |
4 |
2 |
2 |
3 |
2 |
0 |
23 |
| Baikalsjön – sjön utan like i ålder, djup och klarhet. | 0 |
0 |
3 |
0 |
1 |
1 |
0 |
0 |
0 |
0 |
2 |
1 |
8 |
| Barriers against wear affect the spatial distribution of tree saplings in urban woodlands | 0 |
1 |
5 |
0 |
3 |
1 |
1 |
2 |
5 |
2 |
4 |
3 |
27 |
| Bibliometric evaluation of Finnish astronomy | 2 |
3 |
0 |
0 |
1 |
3 |
2 |
4 |
2 |
1 |
2 |
3 |
23 |
| Biodiversity monitoring for decision-making | 1 |
1 |
7 |
5 |
6 |
5 |
13 |
5 |
4 |
0 |
3 |
0 |
50 |
| Biological requirements for storing and transporting barerooted Scots Pine transplants. | 0 |
3 |
1 |
0 |
1 |
0 |
0 |
0 |
2 |
0 |
0 |
0 |
7 |
| Biology of the Baltic smelt (Osmerus eperlanus L.) [Abstract] | 2 |
1 |
4 |
1 |
1 |
0 |
1 |
5 |
0 |
1 |
2 |
1 |
19 |
| Biology of the Baltic smelt (Osmerus eperlanus L.) [Abstract] | 2 |
0 |
0 |
1 |
1 |
1 |
3 |
1 |
0 |
2 |
3 |
1 |
15 |
| Biomass and Carbon Budget of European Forests, 1971 to 1990 | 15 |
17 |
9 |
16 |
8 |
8 |
5 |
2 |
5 |
7 |
3 |
0 |
95 |
| Blomkålssjukan hos ål finns redan i våra vatten | 1 |
2 |
0 |
1 |
5 |
3 |
0 |
1 |
0 |
2 |
1 |
1 |
17 |
| Boreal Carabid Beetles (Coleoptera, Carabidae) in Managed Spruce Forests : a Summary of Finnish Case Studies | 1 |
2 |
7 |
1 |
2 |
4 |
2 |
9 |
3 |
2 |
1 |
2 |
36 |
| Boreal carabid-beetle (Coleoptera, Carabidae) assemblages along the clear-cut originated succession gradient | 2 |
4 |
12 |
5 |
3 |
5 |
6 |
5 |
4 |
5 |
2 |
2 |
55 |
| Boreal Forests and a Possible Climatic Warming | 0 |
4 |
1 |
1 |
2 |
0 |
0 |
1 |
1 |
0 |
1 |
2 |
13 |
| Boreal Forests and the Global Carbon Cycle | 7 |
5 |
1 |
0 |
0 |
0 |
1 |
2 |
1 |
2 |
1 |
2 |
22 |
| Bottendjuren i Tvärminne som miljöindikatorer | 0 |
2 |
2 |
2 |
0 |
1 |
3 |
1 |
1 |
1 |
3 |
0 |
16 |
| Bringing Feedback and Resilience of High-latitude Ecosystems into the Corporate Boardroom | 7 |
0 |
4 |
1 |
1 |
7 |
6 |
3 |
2 |
1 |
1 |
0 |
33 |
| C and N storage in living trees within Finland since 1950s | 2 |
8 |
4 |
6 |
8 |
4 |
9 |
2 |
6 |
1 |
3 |
1 |
54 |
| Cadmium and Mercury in Macrofungi : Mechanisms of Transport and Accumulation | 1 |
5 |
3 |
8 |
4 |
10 |
2 |
2 |
1 |
2 |
0 |
4 |
42 |
| Cadmium concentration in edible Baltic fish | 0 |
2 |
1 |
0 |
0 |
2 |
0 |
1 |
0 |
0 |
1 |
3 |
10 |
| Cadmium concentrations in Boreal Forest Ecosystem After Application of Wood Ash | 3 |
0 |
4 |
0 |
3 |
0 |
1 |
0 |
4 |
0 |
1 |
1 |
17 |
| Cadmium in Forest Mushrooms After Application of Wood Ash | 1 |
2 |
1 |
1 |
1 |
3 |
4 |
3 |
1 |
1 |
2 |
3 |
23 |
| Cadmium in insects after ash fertilization | 3 |
3 |
4 |
4 |
5 |
0 |
2 |
3 |
1 |
0 |
5 |
1 |
31 |
| Carabid beetle and spider assemblages along a forested urban–rural gradient in southern Finland | 1 |
5 |
4 |
1 |
4 |
4 |
0 |
0 |
1 |
1 |
0 |
0 |
21 |
| Carabid beetle assemblages (Coleoptera, Carabidae) across urban-rural gradients : an international comparison | 4 |
5 |
15 |
4 |
10 |
6 |
3 |
4 |
3 |
3 |
3 |
3 |
63 |
| Carbon balance in East European tundra | 1 |
0 |
1 |
1 |
5 |
0 |
2 |
4 |
0 |
1 |
2 |
1 |
18 |
| Carbon Budget Estimates (Response) | 2 |
1 |
1 |
4 |
3 |
0 |
1 |
0 |
2 |
1 |
3 |
3 |
21 |
| Carbon Reservoirs in Peatlands and Forests in the Boreal Regions of Finland | 1 |
2 |
4 |
2 |
2 |
6 |
2 |
3 |
2 |
1 |
2 |
2 |
29 |
| Cd, Fe and Zn Content of the Epiphytic Lichen Hypogymnia Physodes in a Finnish Suburb | 2 |
3 |
4 |
6 |
4 |
1 |
3 |
2 |
6 |
0 |
3 |
1 |
35 |
| Center and surround excitation in the receptive fields of frog retinal ganglion cells | 2 |
2 |
3 |
2 |
1 |
4 |
3 |
0 |
0 |
2 |
3 |
1 |
23 |
| Changes in carabid beetle assemblages across an urban-rural gradient in Japan | 5 |
3 |
4 |
3 |
0 |
7 |
2 |
1 |
3 |
2 |
4 |
1 |
35 |
| Changes in expression and honesty of sexual signalling over the reproductive lifetime of sticklebacks | 1 |
1 |
1 |
0 |
1 |
0 |
1 |
1 |
1 |
0 |
3 |
2 |
12 |
| Changes in retinal time scale under background light : observations on rods and ganglion cells in the frog retina | 0 |
0 |
0 |
0 |
0 |
1 |
0 |
0 |
0 |
1 |
0 |
0 |
2 |
| Changes in the light-sensitive current of salamander rods upon manipulation of putative pH-regulating mechanisms in the inner and outer segment | 2 |
2 |
3 |
1 |
1 |
1 |
2 |
0 |
0 |
4 |
4 |
4 |
24 |
| Characterization and source identification of a fine particle episode in Finland | 1 |
1 |
1 |
1 |
3 |
2 |
3 |
2 |
3 |
4 |
5 |
4 |
30 |
| Characterization and source identification of a fine particle episode in Finland | 4 |
1 |
4 |
1 |
3 |
4 |
3 |
1 |
4 |
3 |
8 |
2 |
38 |
| Characterization of aerosol particle episodes in Finland caused by wildfires in Eastern Europe | 4 |
1 |
3 |
1 |
3 |
8 |
4 |
1 |
1 |
1 |
1 |
0 |
28 |
| Characterization of surface glycoproteins of mouse lymphoid cells | 3 |
0 |
1 |
1 |
1 |
0 |
3 |
1 |
0 |
1 |
1 |
0 |
12 |
| Chlorinated Insecticide Residues in Tanzanian Environment. Tanzadrin. | 1 |
0 |
1 |
3 |
1 |
3 |
4 |
0 |
3 |
1 |
2 |
1 |
20 |
| Chromophore switch from 11-cis-dehydroretinal (A2) to 11-cis-retinal (A1) decreases dark noise in salamander red rods | 2 |
0 |
1 |
3 |
0 |
4 |
2 |
2 |
0 |
2 |
4 |
2 |
22 |
| Climate and traffic : prospects for Finland | 2 |
1 |
1 |
2 |
1 |
0 |
2 |
1 |
0 |
1 |
2 |
0 |
13 |
| Climate change and macrolepidopteran biodiversity in Finland | 4 |
3 |
6 |
3 |
1 |
3 |
1 |
2 |
7 |
6 |
3 |
3 |
42 |
| Coleopteran diversity and abundance in different habitats near Kihansi waterfall, in the Udzungwa Mountains, Tanzania | 1 |
1 |
1 |
0 |
1 |
4 |
7 |
1 |
3 |
1 |
3 |
2 |
25 |
| Colonization success of carabid beetles on Baltic islands | 0 |
0 |
5 |
1 |
2 |
0 |
1 |
2 |
2 |
2 |
2 |
4 |
21 |
| Combinatorial Approaches for Mass Spectra Recalibration | 2 |
4 |
4 |
3 |
4 |
3 |
2 |
1 |
4 |
4 |
8 |
8 |
47 |
| Compressed Suffix Arrays for Massive Data | 10 |
6 |
7 |
5 |
6 |
2 |
11 |
10 |
8 |
15 |
8 |
13 |
101 |
| Concentrations of heavy metals in fish from coastal waters around the Baltic Sea (Extended abstract) | 1 |
2 |
2 |
2 |
0 |
1 |
0 |
1 |
7 |
0 |
1 |
7 |
24 |
| Concentrations of heavy metals in fishes from coastal waters around the Baltic Sea | 1 |
1 |
2 |
1 |
1 |
3 |
1 |
3 |
2 |
3 |
1 |
2 |
21 |
| Concentrations of heavy metals in sediment and benthos of Tvärminne Sorfjärd, Finnish western Gulf of Finland (Baltic Sea). | 2 |
2 |
2 |
1 |
3 |
1 |
0 |
0 |
0 |
0 |
2 |
4 |
17 |
| Concentrations of heavy metals in viviparous blenny (Zoarces viviparous L.) and flounder (Platichthys flesus L.) from Finnish coastal waters and their possible harmful effect on the health condition of the fishes [Abstract] | 0 |
2 |
3 |
4 |
3 |
0 |
1 |
2 |
0 |
1 |
2 |
0 |
18 |
| Concentrations of Heavy metals, in sediment and biota, from coastal waters, at Tvärminne, Finnish western Gulf of Finland | 1 |
1 |
4 |
2 |
2 |
1 |
1 |
1 |
0 |
1 |
0 |
0 |
14 |
| Concentrations of mercury (Hg) and cadmium (Cd) in some coastal fishes from Gulf of Finland : Baltic herring (Clupea harengus membras L.), smelt (Osmerus eperlanus L.), perch (Perca fluviatilis L.), eelpout (Zoarces viviparus L.), flounder (Platichtys flesus L.) and four-horned sculpin (Myoxocephalus quadricornis L.) in Finnish and Estonian waters. | 0 |
1 |
4 |
2 |
0 |
1 |
0 |
2 |
2 |
2 |
2 |
0 |
16 |
| Concentrations of mercury (Hg) and cadmium (Cd) in the Baltic eelpout (Zoarces viviparus L.) from the Gulf of Riga (Latvia) and the archipelago sea (SW Finland), including a parasitological remark | 0 |
1 |
1 |
2 |
1 |
0 |
1 |
3 |
1 |
0 |
5 |
2 |
17 |
| Concentrations of Mercury and Cadmium in Perch (Perca fluviatilis L.), Ruffe (Gymnocephalus cernuus L.), Three-spined Stickleback (Gasterosteus aculaeatus L.), and Nine-spined Stickleback (Pungitius pungitius L.), from SW Finnish Coastal Waters | 0 |
2 |
2 |
93 |
2 |
2 |
6 |
10 |
0 |
1 |
1 |
1 |
120 |
| Concentrations of mercury and cadmium in some coastal fishes from the Finnish and Estonian parts of the Gulf of Finland | 0 |
1 |
1 |
1 |
1 |
3 |
0 |
2 |
1 |
0 |
0 |
2 |
12 |
| Concentrations of nickel (Ni) in some coastal Baltic fishes | 0 |
1 |
3 |
2 |
4 |
0 |
4 |
2 |
5 |
2 |
2 |
0 |
25 |
| Connectivity, probabilities and persistence : comparing reserve selection strategies | 1 |
2 |
3 |
1 |
5 |
4 |
2 |
4 |
2 |
2 |
7 |
4 |
37 |
| Conservation contracts in habitat protection in southern Finland | 0 |
0 |
0 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
| Conservation implications of exporting domestic wood harvest to neighboring countries | 3 |
3 |
1 |
3 |
1 |
3 |
2 |
1 |
1 |
0 |
3 |
1 |
22 |
| Continental impact on marine boundary layer coarse particles over the Atlantic Ocean between Europe and Antarctica | 2 |
3 |
1 |
2 |
0 |
3 |
2 |
1 |
0 |
3 |
2 |
9 |
28 |
| Contribution of the temperate forests to the world's carbon budget | 8 |
2 |
4 |
2 |
1 |
3 |
2 |
3 |
1 |
0 |
0 |
1 |
27 |
| Cooperative behaviour and cooperative breeding : What constitutes an explanation? | 1 |
6 |
1 |
6 |
0 |
2 |
4 |
12 |
4 |
1 |
3 |
4 |
44 |
| Coordinating concurrent transmissions : a constant-factor approximation of maximum-weight independent set in local conflict graphs | 0 |
2 |
2 |
0 |
2 |
3 |
4 |
0 |
1 |
1 |
3 |
6 |
24 |
| Correlation between male size and territory quality : consequence of male competition or predation risk? | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
2 |
| Correlation between male size and territory quality : consequence of male competition or predation susceptibility? | 2 |
4 |
5 |
3 |
7 |
4 |
5 |
4 |
2 |
4 |
5 |
8 |
53 |
| Development and survival of a specialist herbivore, Melitaea cinxia, on host plants producing high and low concentrations of iridoid glycosides | 1 |
0 |
1 |
1 |
0 |
1 |
0 |
1 |
2 |
0 |
1 |
1 |
9 |
| Development and survival of a specialist herbivore, Melitaea cinxia, on host plants producing high and low concentrations of iridoid glycosides. | 0 |
1 |
1 |
0 |
0 |
6 |
4 |
0 |
1 |
1 |
2 |
1 |
17 |
| Diatom and Metal Stratigraphy of a Small and Shallow Lake in Southern Finland | 1 |
1 |
2 |
0 |
4 |
0 |
3 |
3 |
1 |
0 |
0 |
1 |
16 |
| Disaggregative Policy Delphi : Using cluster analysis as a tool for systematic scenario formation | 2 |
52 |
4 |
0 |
2 |
3 |
2 |
2 |
1 |
3 |
4 |
2 |
77 |
| Diseases of fish in the Tvärminne area [Abstract] | 0 |
2 |
2 |
3 |
2 |
1 |
2 |
2 |
0 |
3 |
2 |
1 |
20 |
| Distribution of Airborne Particles from Multi-Emission Source | 1 |
0 |
1 |
0 |
1 |
0 |
0 |
0 |
1 |
3 |
1 |
0 |
8 |
| Distribution of carabid Beetles (Coleoptera, Carabidae) across a Boreal Forest-Clearcut Ecotone | 1 |
1 |
3 |
4 |
0 |
2 |
1 |
5 |
2 |
1 |
0 |
0 |
20 |
| Do males matter? : The role of males in population dynamics | 6 |
4 |
7 |
6 |
6 |
3 |
3 |
25 |
3 |
8 |
4 |
0 |
75 |
| Does the random distribution of discrete photoreceptor events limit the sensitivity of the retina? | 2 |
2 |
2 |
1 |
2 |
3 |
3 |
2 |
1 |
0 |
3 |
1 |
22 |
| Dry and wet deposition of mercury near a chlor-alkali plant | 0 |
0 |
2 |
1 |
0 |
2 |
0 |
1 |
0 |
1 |
1 |
3 |
11 |
| Duger spånakäringen som miljöbioindikatororganism? | 1 |
3 |
2 |
2 |
3 |
0 |
3 |
1 |
3 |
4 |
5 |
1 |
28 |
| Dynamics of local expansion by an introduced species : Pterostichus melanarius III. (Coleoptera, Carabidae) in Alberta Canada. | 3 |
1 |
3 |
1 |
3 |
3 |
1 |
2 |
3 |
1 |
0 |
3 |
24 |
| Ecology and urban planning | 25 |
124 |
109 |
34 |
41 |
33 |
29 |
56 |
23 |
5 |
1 |
2 |
482 |
| Effect of Acidification on Metal Uptake of Picea abies Seedlings | 2 |
3 |
4 |
1 |
3 |
4 |
5 |
3 |
3 |
5 |
7 |
3 |
43 |
| Effect of background luminance on visual responses to strong flashes : perceived brightness and the early rise of photoreceptor responses | 2 |
1 |
2 |
4 |
2 |
3 |
3 |
2 |
1 |
3 |
2 |
1 |
26 |
| Effects of a hydropower plant on Coleopteran diversity and abundance in the Udzungwa Mountains, Tanzania | 4 |
2 |
2 |
3 |
2 |
2 |
6 |
1 |
2 |
2 |
4 |
8 |
38 |
| Effects of Acidification on the Mobilization of Cadmium and Mercury from Soils | 2 |
3 |
6 |
5 |
3 |
6 |
2 |
0 |
0 |
3 |
3 |
1 |
34 |
| Effects of Ash Application on Cadmium Concentration in Small Mammals | 1 |
1 |
0 |
1 |
5 |
0 |
1 |
0 |
0 |
0 |
2 |
1 |
12 |
| Effects of habitat fragmentation at different trophic levels in insect communities | 3 |
0 |
2 |
6 |
3 |
5 |
6 |
2 |
2 |
5 |
5 |
3 |
42 |
| Effects of sulfhydryl binding reagents on the photoresponses of amphibian retinal rods | 4 |
2 |
2 |
3 |
7 |
1 |
3 |
4 |
0 |
1 |
5 |
1 |
33 |
| Elämän suolaa metsästä | 1 |
4 |
1 |
1 |
0 |
1 |
0 |
0 |
0 |
1 |
0 |
1 |
10 |
| Environmental impact of photovoltaic electrification in rural areas | 0 |
3 |
1 |
0 |
1 |
0 |
0 |
1 |
1 |
1 |
0 |
1 |
9 |
| Environmental Mercury Contamination Around Chlor-Alkali Plant | 2 |
4 |
5 |
2 |
1 |
2 |
1 |
4 |
1 |
2 |
4 |
4 |
32 |
| Epistemology and public policy : Using a new typology to analyse the paradigm shift in Finnish transport futures research | 1 |
2 |
3 |
1 |
3 |
3 |
1 |
0 |
1 |
5 |
6 |
5 |
31 |
| Estimating Biomass (Response) | 0 |
1 |
3 |
1 |
3 |
0 |
0 |
3 |
1 |
1 |
1 |
0 |
14 |
| Eutrofieringen och saltvatteninflödet | 0 |
1 |
4 |
0 |
4 |
0 |
1 |
1 |
1 |
0 |
0 |
1 |
13 |
| Evaluation of the importance of acclimation of needle structure, photosynthesis, and respiration to available photosynthetically active radiation in a Scots pine canopy | 12 |
61 |
3 |
0 |
1 |
0 |
1 |
1 |
1 |
1 |
1 |
0 |
82 |
| Evolution of frequency-dependent mate choice : keeping up with fashion trends. | 2 |
1 |
1 |
0 |
1 |
1 |
0 |
2 |
1 |
1 |
1 |
1 |
12 |
| Evolution of migration rate in a spatially realistic metapopulation model. | 0 |
0 |
0 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
| Exchange of mercury between atmosphere and vegetation under contaminated conditions | 4 |
0 |
3 |
1 |
1 |
0 |
0 |
1 |
2 |
1 |
0 |
1 |
14 |
| Experimental confirmation that inbreeding depression increases extinction risk in butterfly populations. | 4 |
1 |
2 |
4 |
2 |
3 |
2 |
1 |
1 |
1 |
1 |
5 |
27 |
| Experimental evaluation of nutrient limitation of phytoplankton communities in the Gulf of Riga | 1 |
0 |
1 |
0 |
0 |
2 |
1 |
1 |
2 |
2 |
2 |
3 |
15 |
| Experimental studies about the impact of traction sand on urban road dust composition | 0 |
0 |
2 |
2 |
2 |
5 |
1 |
3 |
1 |
1 |
4 |
1 |
22 |
| Extinction threshold in metapopulation models | 1 |
2 |
4 |
6 |
2 |
6 |
12 |
13 |
6 |
2 |
3 |
8 |
65 |
| Extinction-colonization dynamics and host-plant choice in butterfly metapopulations. | 0 |
0 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
| Fast Index Based Filters for Music Retrieval | 2 |
0 |
1 |
2 |
2 |
0 |
0 |
1 |
0 |
2 |
1 |
0 |
11 |
| Fatty acids on continental sulfate aerosol particles | 1 |
2 |
3 |
2 |
2 |
2 |
0 |
2 |
2 |
1 |
1 |
0 |
18 |
| Feathers of birds of prey as indicators of mercury contamination in southern Finland | 2 |
1 |
0 |
2 |
1 |
3 |
0 |
1 |
1 |
2 |
2 |
0 |
15 |
| Field crops in a CO2-enriched atmosphere. | 0 |
0 |
4 |
1 |
1 |
1 |
1 |
4 |
1 |
1 |
2 |
4 |
20 |
| Fish surveys in the Väike Väin strait between the islands of Saaremaa and Muhu, Western Estonia | 1 |
4 |
2 |
2 |
2 |
2 |
0 |
1 |
1 |
4 |
3 |
1 |
23 |
| Flicker sensitivity as a function of the spectral density of external white temporal noise | 583 |
3 |
1 |
1 |
2 |
4 |
3 |
3 |
2 |
1 |
0 |
1 |
604 |
| Flows of nitrogen and phosphorus in municipal waste : a substance flow analysis in Finland | 4 |
3 |
9 |
4 |
6 |
7 |
11 |
10 |
12 |
8 |
11 |
10 |
95 |
| Fluktuationer i fisk- och bottendjurfaunan i Tvärminne Storfjärd, enligt anteckningar i loggböckerna från RV "J.A. Palmé" (1975-1986) och RV ”Saduria” (1987-2005), Tvärminne zoologiska station. | 2 |
3 |
2 |
2 |
1 |
2 |
107 |
2 |
1 |
2 |
3 |
1 |
128 |
| Forest resources in Finland and findings on the impacts of air pollution on forests | 0 |
1 |
1 |
1 |
0 |
4 |
1 |
1 |
1 |
4 |
2 |
3 |
19 |
| Forests and the Changing Chemical Composition of the Atmosphere | 5 |
2 |
4 |
5 |
1 |
3 |
1 |
1 |
4 |
1 |
2 |
2 |
31 |
| Formation of HArF in solid Ar revisited : Are mobile vacancies involved in the matrix-site conversion at 30 K? | 48 |
24 |
1 |
0 |
0 |
1 |
0 |
0 |
0 |
0 |
4 |
2 |
80 |
| From individual behavior to metapopulation dynamics : unifying the patchy population and classic metapopulation models. | 0 |
0 |
1 |
0 |
0 |
0 |
1 |
1 |
0 |
0 |
1 |
0 |
4 |
| Förändringar i den västnyländska fiskmiljön | 0 |
0 |
0 |
0 |
2 |
1 |
2 |
5 |
0 |
2 |
0 |
1 |
13 |
| Förändringar i kustfiskfaunan | 1 |
0 |
2 |
1 |
1 |
0 |
1 |
0 |
0 |
1 |
0 |
0 |
7 |
| Ganglion cell performance at absolute threshold in toad retina : effects of dark events in rods | 3 |
2 |
1 |
3 |
3 |
0 |
2 |
2 |
5 |
5 |
3 |
1 |
30 |
| Gap felling as a forest harvesting method in boreal forests : responses of carabid beetles (Coleoptera, Carabidae) | 3 |
1 |
1 |
3 |
0 |
2 |
2 |
1 |
0 |
1 |
0 |
0 |
14 |
| Gennarbyviken och Gennarbyviksbassängen | 3 |
8 |
4 |
2 |
0 |
2 |
1 |
2 |
1 |
0 |
0 |
6 |
29 |
| Give the climate issue back to the researchers | 0 |
1 |
1 |
1 |
0 |
0 |
0 |
1 |
0 |
0 |
1 |
0 |
5 |
| Gradients of vibrational coordinates from the variation of coordinates along the path of a particle | 0 |
1 |
2 |
1 |
0 |
1 |
2 |
0 |
1 |
0 |
0 |
0 |
8 |
| Ground beetles (Coleoptera: Carabidae) as bioindicators | 11 |
11 |
25 |
21 |
31 |
19 |
23 |
20 |
14 |
8 |
13 |
5 |
201 |
| Habitat use by endemic and introduced rodents along a gradient of forest disturbance in Madagascar | 2 |
3 |
5 |
2 |
3 |
2 |
3 |
1 |
2 |
5 |
0 |
0 |
28 |
| Hair Mercury Contents and Fish Eating Habits of People Living Near a Finnish Man-made Lake | 5 |
1 |
2 |
6 |
7 |
4 |
5 |
5 |
5 |
3 |
4 |
3 |
50 |
| Heavy Metal (Hg, Cd, Zn) Concentrations and Condition of Eelpout (Zoarces viviparus L.), around Baltic Sea | 4 |
8 |
4 |
6 |
1 |
3 |
4 |
4 |
0 |
1 |
4 |
3 |
42 |
| Heavy Metal and Organochlorine levels in coastal fishes from the Väike Väin strait, western Estonia, in high summers of 1993-94. | 4 |
3 |
5 |
3 |
0 |
4 |
9 |
15 |
3 |
4 |
4 |
3 |
57 |
| Heavy metal concentrations and condition of Baltic fishes | 0 |
0 |
6 |
5 |
3 |
1 |
3 |
3 |
2 |
4 |
1 |
1 |
29 |
| Heavy metal concentrations in four-horn sculpin Triglopsis quadricornis (L.) (Pisces), its main food organism Saduria entomon L. (Crustacea), and in bottom sediments in the Archipelago Sea and the Gulf of Finland (Baltic Sea) | 1 |
1 |
2 |
1 |
0 |
0 |
2 |
3 |
4 |
2 |
2 |
2 |
20 |
| Heavy metal concentrations in males and females of three pine diprionids (Hymenoptera) | 2 |
1 |
3 |
2 |
3 |
5 |
4 |
1 |
3 |
2 |
0 |
3 |
29 |
| Heavy Metal Levels in Two Biennial Pine Insects With Sap-Sucking and Gal-Forming Life-Styles | 0 |
5 |
3 |
2 |
5 |
2 |
2 |
4 |
2 |
61 |
51 |
23 |
160 |
| Heavy metal solubility in podzolic soils exposed to the alkalizing effect of air pollutants. | 3 |
1 |
3 |
0 |
1 |
1 |
5 |
6 |
0 |
2 |
2 |
2 |
26 |
| Heavy Metals in Epiphytic Vegetation of Arusha, N. Tanzania | 3 |
4 |
3 |
5 |
1 |
2 |
5 |
1 |
3 |
2 |
6 |
4 |
39 |
| Heavy metals in Finnish honey, pollen and honey bees | 7 |
4 |
25 |
14 |
29 |
24 |
11 |
16 |
4 |
6 |
11 |
2 |
153 |
| Heavy metals in the Baltic Sea environment and the condition of coastal fishes around the Baltic Sea (Abstract) | 0 |
3 |
0 |
1 |
0 |
0 |
0 |
2 |
1 |
3 |
1 |
1 |
12 |
| High summer concentrations of mercury in big perch (Perca fluviatilis L) from the Tvärminne archipelago (SW Finland) and Nåtö (Åland Islands) Baltic Sea | 1 |
2 |
3 |
1 |
0 |
0 |
0 |
1 |
2 |
0 |
3 |
0 |
13 |
| Honey, Pollen and Bees as Indicator of Heavy Metal Pollution | 7 |
6 |
4 |
6 |
10 |
18 |
8 |
13 |
3 |
2 |
1 |
4 |
82 |
| Host plants as islands : Resource quality and spatial setting as determinants of insect distribution | 1 |
1 |
3 |
1 |
3 |
1 |
2 |
2 |
2 |
0 |
5 |
0 |
21 |
| How partnerships end in guillemots Uria aalge : chance events, adaptive change, or forced divorce? | 2 |
1 |
1 |
3 |
1 |
0 |
1 |
2 |
1 |
0 |
2 |
4 |
18 |
| How the latencies of excitation and inhibition determine ganglion cell thresholds and discharge patterns in the frog | 1 |
1 |
1 |
3 |
2 |
2 |
4 |
3 |
4 |
2 |
4 |
0 |
27 |
| Human hair mercury levels in Tucuruí area, State of Pará, Brazil | 2 |
1 |
1 |
3 |
1 |
5 |
1 |
4 |
3 |
2 |
1 |
2 |
26 |
| HXeCCH in Ar and Kr matrices | 2 |
2 |
1 |
2 |
1 |
1 |
3 |
1 |
0 |
1 |
1 |
0 |
15 |
| Höttern, eller blåstången (Fucus vesiculosus L.) som miljöindikator | 2 |
2 |
1 |
4 |
2 |
1 |
3 |
9 |
0 |
3 |
2 |
4 |
33 |
| Identification of an organic coating on marine aerosol particles by TOF-SIMS | 4 |
105 |
3 |
9 |
3 |
5 |
5 |
5 |
3 |
4 |
4 |
1 |
151 |
| Illegal wildlife trade in the Himalayan region of China | 10 |
0 |
6 |
7 |
18 |
8 |
7 |
30 |
9 |
9 |
15 |
7 |
126 |
| Ilmastopolitiikan perustuttava tietoon | 0 |
0 |
1 |
2 |
0 |
2 |
0 |
1 |
1 |
0 |
0 |
3 |
10 |
| Impact of climatic change on the values of effective temperature sum. | 0 |
1 |
1 |
2 |
2 |
0 |
3 |
2 |
1 |
4 |
0 |
2 |
18 |
| Impact of forests on net national emissions of carbon dioxide in west Europe | 1 |
0 |
3 |
1 |
6 |
6 |
2 |
11 |
3 |
2 |
1 |
5 |
41 |
| Impact of reindeer grazing on ground-dwelling Carabidae and Curculionidae assemblages in Lapland | 2 |
1 |
0 |
2 |
5 |
6 |
3 |
5 |
2 |
0 |
4 |
6 |
36 |
| Importing Timber, Exporting Ecological Impact | 3 |
0 |
2 |
0 |
0 |
1 |
0 |
0 |
2 |
0 |
0 |
1 |
9 |
| In search of the visual pigment template | 6 |
7 |
3 |
98 |
13 |
25 |
14 |
4 |
7 |
6 |
10 |
12 |
205 |
| In Situ Bioremediation through Mulching of Soil Polluted by a Copper–Nickel Smelter | 1 |
1 |
5 |
1 |
0 |
3 |
3 |
1 |
1 |
2 |
0 |
2 |
20 |
| In the midst of ecology, conservation, and competing interests in the society. | 1 |
3 |
3 |
2 |
2 |
0 |
1 |
2 |
4 |
1 |
1 |
1 |
21 |
| Increased Carbon Sink in Temperate and Boreal Forests | 4 |
3 |
1 |
3 |
6 |
2 |
4 |
3 |
5 |
4 |
1 |
1 |
37 |
| Increased signalling effort when survival prospects decrease : male-male competition ensures honesty | 0 |
0 |
1 |
1 |
0 |
2 |
0 |
3 |
2 |
0 |
1 |
1 |
11 |
| Indirect effects of least weasel presence on field vole behaviour and demography : a field experiment. | 0 |
2 |
2 |
0 |
0 |
1 |
0 |
2 |
1 |
0 |
1 |
1 |
10 |
| Influence of a Chlor-Alkali Plant on the Mercury Content of Fungi | 2 |
2 |
3 |
2 |
3 |
0 |
0 |
0 |
2 |
1 |
2 |
0 |
17 |
| Influence of species, sex, age and food for the accumulation of toxic cadmium and some other metals in Auchennorhynchous Homoptera | 6 |
4 |
4 |
3 |
2 |
5 |
3 |
7 |
3 |
4 |
5 |
2 |
48 |
| Inhibition of β2 Integrin–mediated Leukocyte Cell Adhesion | 2 |
4 |
1 |
0 |
1 |
3 |
1 |
3 |
1 |
1 |
4 |
1 |
22 |
| Integrated Analysis of Acidification in Europe. | 2 |
3 |
1 |
3 |
4 |
0 |
1 |
4 |
1 |
2 |
1 |
2 |
24 |
| Interaction of rare-gas-containing molecules with nitrogen : Matrix-isolation and ab initio study of HArF⋯N₂, HKrF⋯N₂, and HKrCl⋯N₂ complexes | 3 |
0 |
1 |
3 |
2 |
0 |
2 |
3 |
5 |
2 |
3 |
1 |
25 |
| Intercellular Adhesion Molecule-5 Induces Dendritic Outgrowth by Homophilic Adhesion | 4 |
2 |
3 |
2 |
0 |
1 |
4 |
0 |
4 |
3 |
5 |
4 |
32 |
| Inälvsparasiter från nors (Pisces, Osmerus eperlanus) från Finlands kustvatten | 1 |
4 |
2 |
4 |
2 |
5 |
4 |
1 |
3 |
1 |
4 |
0 |
31 |
| Is there a need for a theory of urban ecology? | 5 |
8 |
8 |
5 |
14 |
9 |
13 |
8 |
7 |
11 |
5 |
13 |
106 |
| Iskusanat eivät suojele ympäristöä | 1 |
2 |
1 |
0 |
1 |
0 |
0 |
4 |
0 |
1 |
2 |
0 |
12 |
| Itämerensimpukka (Macoma baltica L.) metallikuormitusten indikaattorina | 2 |
4 |
5 |
0 |
6 |
1 |
0 |
2 |
0 |
1 |
1 |
1 |
23 |
| Ivrig forskning kring gåtfull ål | 0 |
1 |
2 |
1 |
2 |
2 |
1 |
0 |
2 |
0 |
3 |
2 |
16 |
| Kadmiumförekomster i fisk | 0 |
2 |
1 |
0 |
1 |
1 |
0 |
1 |
0 |
1 |
0 |
0 |
7 |
| Kadmiumkoncentrationer i muskulatur, lever, njure, mjälte, galla och gonader hos åländsk flundra (Platichthys flesus L.) | 2 |
2 |
1 |
1 |
1 |
1 |
1 |
2 |
2 |
0 |
0 |
0 |
13 |
| Kadmiumkoncentrationer i muskulatur, lever, njure, mjälte, galla och gonader hos åländsk flundra (Platichthys flesus L.) | 1 |
4 |
4 |
3 |
2 |
0 |
1 |
2 |
1 |
2 |
2 |
1 |
23 |
| Kaloissamme todettuja lyijypitoisuuksia | 6 |
1 |
2 |
4 |
4 |
5 |
3 |
0 |
1 |
2 |
2 |
2 |
32 |
| Kalojemme kadmiumpitoisuuksia | 0 |
0 |
1 |
0 |
0 |
0 |
0 |
2 |
0 |
0 |
2 |
0 |
5 |
| Kilkki (Saduria entomon L.) ympäristöindikaattorina | 3 |
3 |
2 |
4 |
0 |
4 |
3 |
5 |
3 |
0 |
4 |
5 |
36 |
| Kioto+ mission : Global and accurate monitoring of forest, land cover and carbon | 1 |
0 |
1 |
1 |
0 |
1 |
0 |
0 |
1 |
1 |
1 |
0 |
7 |
| Kustvattenfiskens kvicksilverbelastning och kondition | 1 |
2 |
2 |
0 |
0 |
0 |
0 |
1 |
1 |
0 |
1 |
5 |
13 |
| Kylmälaboratorion suurmies | 0 |
1 |
2 |
0 |
1 |
0 |
1 |
6 |
1 |
2 |
1 |
0 |
15 |
| Large blueshift of the H–Kr stretching frequency of HKrCl upon complexation with N₂ | 2 |
0 |
3 |
2 |
6 |
3 |
3 |
0 |
2 |
0 |
3 |
1 |
25 |
| Large-scale dynamics of the Glanville fritillary butterfly : landscape structure, population processes, and weather | 0 |
2 |
2 |
0 |
2 |
1 |
4 |
1 |
2 |
1 |
0 |
0 |
15 |
| Leaching of Mercury from Peat Soil | 0 |
2 |
4 |
5 |
3 |
1 |
3 |
3 |
1 |
1 |
3 |
1 |
27 |
| Lead, cadmium and mercury contents of Fungi in Mikkeli, SE Finland | 1 |
2 |
2 |
1 |
3 |
2 |
2 |
7 |
5 |
2 |
6 |
3 |
36 |
| Lead, Cadmium, and Mercury Contents of Fungi in Helsinki Area and in Unpolluted Control Areas | 6 |
13 |
4 |
2 |
2 |
3 |
3 |
2 |
2 |
4 |
1 |
2 |
44 |
| Leaf litter and the small-scale distribution of carabid beetles (Coleoptera, Carabidae) in the boreal forest | 3 |
2 |
2 |
4 |
8 |
4 |
7 |
3 |
6 |
3 |
4 |
3 |
49 |
| Letters: The benefits of CCS | 1 |
1 |
1 |
1 |
1 |
2 |
0 |
2 |
1 |
1 |
2 |
3 |
16 |
| Light responses and light adaptation in rat retinal rods at different temperatures | 0 |
0 |
1 |
1 |
1 |
2 |
1 |
5 |
3 |
4 |
3 |
4 |
25 |
| Long-Term Dynamics in a Metapopulation of the American Pika | 11 |
1 |
3 |
0 |
6 |
3 |
7 |
3 |
1 |
0 |
2 |
0 |
37 |
| Low retinal noise in animals with low body temperature allows high visual sensitivity | 4 |
5 |
5 |
6 |
2 |
10 |
5 |
9 |
7 |
4 |
6 |
7 |
70 |
| Luennolle vasta yhdeksäksi | 1 |
2 |
2 |
1 |
1 |
1 |
1 |
1 |
2 |
2 |
0 |
5 |
19 |
| Luonnon monimuotoisuuden suojelun tavoitteet ja keinot | 0 |
19 |
0 |
0 |
2 |
0 |
0 |
2 |
1 |
1 |
1 |
2 |
28 |
| Luonnonsuojelu, ympäristönsuojelu ja kestävä kehitys. | 1 |
0 |
4 |
5 |
3 |
1 |
5 |
1 |
0 |
3 |
2 |
2 |
27 |
| Luonnonsuojelun näkökulmasta kotimainen hakkaa tuontipuun | 0 |
0 |
2 |
1 |
3 |
0 |
1 |
1 |
2 |
1 |
1 |
1 |
13 |
| Male-male competition facilitates female choice in sticklebacks | 2 |
1 |
2 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
6 |
| Management in relation to disturbance in the boreal forest | 6 |
1 |
4 |
1 |
7 |
2 |
6 |
2 |
2 |
7 |
5 |
5 |
48 |
| Management of Forests for Mitigation of Greenhouse Gas Emissions | 4 |
4 |
8 |
19 |
17 |
28 |
20 |
20 |
20 |
13 |
14 |
17 |
184 |
| Managing Climate Risk | 1 |
1 |
3 |
7 |
3 |
5 |
2 |
6 |
3 |
2 |
0 |
5 |
38 |
| Mate choice evolution, dominance effects, and the maintenance of genetic variation. | 1 |
1 |
4 |
0 |
1 |
2 |
3 |
0 |
0 |
2 |
3 |
1 |
18 |
| Mera om blomkålssjuka hos ål | 1 |
1 |
1 |
1 |
2 |
2 |
1 |
1 |
1 |
0 |
0 |
0 |
11 |
| Mercury concentrations in an aquatic ecosystem during twenty years following abatement the pollution source | 2 |
2 |
3 |
0 |
0 |
4 |
60 |
2 |
0 |
2 |
2 |
0 |
77 |
| Mercury content of common frogs (Rana Temporaria L.) and common toads (Bufo bufo L.) collected in southern Finland. | 4 |
2 |
6 |
2 |
5 |
3 |
6 |
3 |
3 |
1 |
5 |
3 |
43 |
| Mercury in flounder Platichthys flesus (L.) from Finnish coastal waters | 1 |
1 |
2 |
1 |
4 |
4 |
1 |
2 |
2 |
2 |
4 |
0 |
24 |
| Mercury in the Amazon | 4 |
4 |
7 |
6 |
3 |
2 |
4 |
2 |
2 |
3 |
1 |
3 |
41 |
| Mercury in waste in the European Union : sources, disposal methods and risks | 7 |
1 |
3 |
7 |
4 |
7 |
5 |
6 |
5 |
8 |
6 |
10 |
69 |
| Mercury Pollution Near an Industrial Source in Southwest Finland | 1 |
1 |
3 |
1 |
2 |
2 |
2 |
0 |
1 |
0 |
4 |
2 |
19 |
| Metal contamination at a wood preservation site : characterisation and experimental studies on remediation | 4 |
4 |
1 |
2 |
3 |
0 |
2 |
3 |
4 |
0 |
0 |
1 |
24 |
| Metal pollution of river Msimbazi, Tanzania | 3 |
2 |
1 |
4 |
1 |
1 |
2 |
6 |
1 |
1 |
0 |
2 |
24 |
| Metsien viisas käyttö on väkevää ilmastopolitiikkaa | 0 |
1 |
1 |
1 |
0 |
4 |
0 |
1 |
0 |
0 |
0 |
2 |
10 |
| Metsäaapinen | 2 |
1 |
4 |
3 |
5 |
5 |
6 |
6 |
4 |
4 |
5 |
2 |
47 |
| Metsät mukaan uuteen Kioton sopimukseen | 1 |
2 |
2 |
2 |
3 |
4 |
1 |
0 |
3 |
2 |
4 |
0 |
24 |
| Metsätuhot ja metsävarat, Muistion Metsä 2000-ohjelman tarkistustoimikunnalle | 2 |
1 |
0 |
2 |
0 |
0 |
0 |
1 |
1 |
2 |
1 |
3 |
13 |
| Miljögifter i och sjukdomar hos flundran | 2 |
0 |
2 |
1 |
1 |
2 |
2 |
1 |
0 |
0 |
0 |
1 |
12 |
| Minimum viable metapopulation size. | 4 |
6 |
5 |
8 |
6 |
9 |
21 |
11 |
2 |
1 |
2 |
1 |
76 |
| Modeling the Location of the Forest Line in Northeast European Russia with Remotely Sensed Vegetation and GIS-Based Climate and Terrain Data | 1 |
1 |
0 |
0 |
0 |
1 |
0 |
1 |
0 |
2 |
1 |
2 |
9 |
| Modelling the spatio-temporal modulation response of ganglion cells with difference-of-Gaussians receptive fields : Relation to photoreceptor response kinetics | 3 |
4 |
5 |
11 |
4 |
4 |
2 |
3 |
3 |
6 |
5 |
4 |
54 |
| Molecular-level variation affects population growth in a butterfly metapopulation. | 0 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
| Monetäre Bewertung der wirtschaftlichen Folgen neuartiger Waldschäden anhand internationaler Daten | 1 |
0 |
3 |
1 |
2 |
0 |
1 |
5 |
3 |
2 |
4 |
1 |
23 |
| Monitoring and assessment of forest damage in regional and national scale. | 0 |
2 |
0 |
1 |
1 |
0 |
2 |
0 |
0 |
0 |
1 |
1 |
8 |
| Multiple mating in the Glanville fritillary butterfly : a case of within-generation bet-hedging? | 2 |
2 |
0 |
0 |
0 |
0 |
0 |
3 |
1 |
1 |
3 |
3 |
15 |
| Natural regeneration of trees in urban woodlands | 2 |
4 |
1 |
0 |
0 |
2 |
3 |
3 |
0 |
1 |
15 |
5 |
36 |
| Neutral rare-gas containing charge-transfer molecules in solid matrices : I. HXeCl, HXeBr, HXeI, and HKrCl in Kr and Xe | 90 |
10 |
1 |
3 |
2 |
0 |
0 |
2 |
3 |
0 |
4 |
2 |
117 |
| Neutral rare-gas containing charge-transfer molecules in solid matrices : II. HXeH, HXeD, and DXeD in Xe | 9 |
3 |
1 |
1 |
0 |
1 |
2 |
2 |
2 |
1 |
3 |
2 |
27 |
| Neutral rare-gas containing charge-transfer molecules in solid matrices : III. HXeCN, HXeNC, and HKrCN in Kr and Xe | 2 |
3 |
3 |
16 |
7 |
1 |
3 |
2 |
1 |
1 |
1 |
2 |
42 |
| Neutralization of solvated protons and formation of noble-gas hydride molecules : matrix-isolation indications of tunneling mechanisms? | 0 |
0 |
1 |
0 |
67 |
23 |
4 |
1 |
3 |
3 |
2 |
0 |
104 |
| New evidence of an organic layer on marine aerosols | 3 |
2 |
0 |
0 |
1 |
0 |
0 |
2 |
2 |
3 |
0 |
0 |
13 |
| New, low estimate for carbon stock in global forest vegetation based on inventory data | 0 |
3 |
4 |
2 |
0 |
0 |
0 |
1 |
0 |
0 |
2 |
1 |
13 |
| Nickel- och blyhalter i fisk | 0 |
4 |
3 |
1 |
3 |
1 |
4 |
1 |
3 |
0 |
2 |
1 |
23 |
| Nikkelipitoisuuksia kaloissamme | 0 |
2 |
0 |
2 |
0 |
1 |
2 |
2 |
2 |
0 |
1 |
2 |
14 |
| Nitrogen dynamics in European forest ecosystems : considerations regarding anthropogenic nitrogen depositions. | 0 |
2 |
1 |
0 |
2 |
0 |
1 |
4 |
4 |
2 |
3 |
4 |
23 |
| No effect of a parasite on reproduction in stickleback males : a laboratory artefact? | 0 |
1 |
3 |
1 |
3 |
2 |
1 |
3 |
2 |
0 |
3 |
1 |
20 |
| No effect of a parasite on reproduction in stickleback males : a laboratory artefact? | 3 |
0 |
1 |
1 |
1 |
1 |
2 |
2 |
1 |
2 |
4 |
2 |
20 |
| Noise and the absolute thresholds of cone and rod vision | 7 |
1 |
2 |
3 |
19 |
7 |
4 |
5 |
16 |
4 |
5 |
8 |
81 |
| Noise-equivalent and signal-equivalent visual summation of quantal events in space and time | 0 |
0 |
3 |
0 |
3 |
1 |
2 |
4 |
0 |
1 |
4 |
3 |
21 |
| Oletko saanut kukkakaalitautisia ankeriaita? | 1 |
1 |
1 |
1 |
2 |
4 |
3 |
1 |
0 |
0 |
1 |
1 |
16 |
| On Self-indexing Images : Image Compression with Added Value | 2 |
3 |
2 |
7 |
3 |
0 |
1 |
5 |
2 |
1 |
5 |
0 |
31 |
| On the biology of the Baltic smelt (Osmerus eperlanus L.) [Abstract] | 1 |
2 |
3 |
1 |
4 |
8 |
4 |
2 |
2 |
3 |
3 |
5 |
38 |
| On the biology of the Baltic smelt (Osmerus eperlanus L.) [Abstract] | 0 |
1 |
1 |
1 |
4 |
2 |
2 |
2 |
0 |
1 |
1 |
2 |
17 |
| On the relation between ERG waves and retinal function : Inverted Rod photoresponses from the frog retina | 10 |
3 |
1 |
1 |
2 |
3 |
3 |
4 |
3 |
2 |
0 |
2 |
34 |
| On theoretical predictions of noble-gas hydrides | 1 |
2 |
61 |
1 |
3 |
2 |
5 |
2 |
3 |
0 |
0 |
3 |
83 |
| Open digestion of some plant and fungus materials for mercury analysis using different temperatures and sample sizes | 1 |
1 |
2 |
3 |
2 |
2 |
1 |
3 |
3 |
3 |
3 |
1 |
25 |
| Optical position clamping with predictive control | 3 |
4 |
1 |
0 |
4 |
1 |
1 |
1 |
0 |
1 |
2 |
2 |
20 |
| Organic Aerosols and the Origin of Life : An Hypothesis | 0 |
1 |
1 |
3 |
3 |
1 |
1 |
3 |
3 |
4 |
2 |
2 |
24 |
| Organo-noble-gas hydride compounds HKrCCH, HXeCCH, HXeCC, and HxeCCXeH : Formation mechanisms and effect of 13C isotope substitution on the vibrational properties | 0 |
1 |
2 |
2 |
0 |
1 |
1 |
1 |
2 |
1 |
2 |
1 |
14 |
| Ozone and water deficit reduced growth of Aleppo pine seedlings | 0 |
0 |
2 |
3 |
1 |
1 |
3 |
3 |
3 |
3 |
2 |
3 |
24 |
| Ozone sensitivity of wild field layer plant species of northern Europe. | 0 |
1 |
0 |
1 |
2 |
1 |
1 |
2 |
0 |
2 |
4 |
2 |
16 |
| Palaeoecological evidence of changes in vegetation and climate during the Holocene in the pre-Polar Urals, northeast European Russia | 2 |
0 |
1 |
0 |
1 |
1 |
3 |
4 |
2 |
0 |
1 |
1 |
16 |
| Parasiter funna i nors (Pisces, Osmerus eperlanus) från Tvärminne Storfjärd, Finska Viken | 2 |
1 |
4 |
4 |
1 |
1 |
0 |
3 |
1 |
3 |
6 |
4 |
30 |
| Performance of moth larvae on birch in relation to altitude, climate, host quality and parasitoids | 1 |
5 |
2 |
3 |
4 |
6 |
6 |
4 |
2 |
1 |
4 |
3 |
41 |
| Pesticides and Metals in Lake Jipe, N. Tanzania. | 1 |
9 |
3 |
2 |
5 |
8 |
4 |
6 |
3 |
2 |
5 |
1 |
49 |
| pH and rate of ‘dark’ events in toad retinal rods : test of a hypothesis on the molecular origin of photoreceptor noise | 0 |
0 |
1 |
0 |
1 |
1 |
0 |
0 |
1 |
1 |
1 |
0 |
6 |
| pH changes in frog rods upon manipulation of putative pH-regulating transport mechanisms | 2 |
0 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
0 |
1 |
6 |
| pH regulation in frog cones studied by mass receptor photoresponses from the isolated retina | 3 |
5 |
8 |
5 |
3 |
4 |
11 |
6 |
1 |
5 |
4 |
1 |
56 |
| Phytoplankton pigments and dissolved organic matter distribution in the Gulf of Riga | 0 |
5 |
3 |
0 |
0 |
3 |
1 |
4 |
0 |
1 |
4 |
5 |
26 |
| Piggvaren i våra kustvatten | 2 |
1 |
1 |
2 |
0 |
2 |
1 |
0 |
0 |
1 |
1 |
0 |
11 |
| Poimintoja Helsingin yliopiston Tvärminnen eläintieteellisen aseman tutkimusalusten ”J.A. Palme´nin” (-1986) ja ”Sadurian” (1987-) lokikirjojen kala- ja pohjaeläinsaalismerkinnöistä 1975-2005 | 1 |
0 |
2 |
0 |
0 |
3 |
0 |
0 |
0 |
2 |
0 |
26 |
34 |
| Polymorphism of the rod visual pigment between allopatric populations of the sand goby (Pomatoschistus minutus) : a microspectrophotometric study | 0 |
2 |
1 |
0 |
0 |
0 |
0 |
3 |
1 |
1 |
2 |
3 |
13 |
| Population Persistence and Offspring Fitness in the Rare Bellflower Campanula Cervicaria in Relation to Population Size and Habitat Quality | 0 |
1 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
1 |
0 |
1 |
4 |
| Porin edustan merialueen norssien (kuoreiden) ja kampeloiden raskasmetallipitoisuuksista | 0 |
0 |
0 |
1 |
0 |
0 |
1 |
0 |
0 |
1 |
0 |
0 |
3 |
| Predator-induced nest site preference : safe nests allow courtship in sticklebacks | 0 |
3 |
4 |
0 |
2 |
1 |
1 |
2 |
2 |
0 |
1 |
2 |
18 |
| Promoting by Expertise : A Study on Information Search and Usage in Geographical Research as an Instrument for Marketing Librarianship | 1 |
1 |
2 |
4 |
3 |
3 |
3 |
4 |
2 |
0 |
4 |
3 |
30 |
| Puu palaa ilman tukiakin | 0 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
1 |
0 |
3 |
| Rannikkoalueidemme norssien (Osmerus eperlanus L.) elohopeapitoisuuksia | 0 |
0 |
1 |
8 |
2 |
1 |
1 |
3 |
1 |
3 |
1 |
3 |
24 |
| Recent Increase in Mercury Sedimentation in a Forest Lake Attributable to Peatland Drainage | 1 |
0 |
7 |
1 |
2 |
3 |
1 |
1 |
1 |
2 |
8 |
6 |
33 |
| Receptive fields of frog retinal ganglion cells : response formation and light-dark-adaptation | 1 |
3 |
0 |
2 |
0 |
2 |
3 |
1 |
1 |
2 |
3 |
1 |
19 |
| Red-cell ICAM-4 is a ligand for the monocyte/macrophage integrinCD11c/CD18 : characterization of the binding sites on ICAM-4 | 2 |
2 |
3 |
4 |
2 |
1 |
6 |
0 |
4 |
1 |
3 |
3 |
31 |
| Reducing Greenhouse gases (Response) | 1 |
2 |
2 |
2 |
0 |
1 |
5 |
0 |
0 |
1 |
0 |
0 |
14 |
| Reduction of mercury pollution in the vicinity of a caustic soda plant in Thailand | 5 |
1 |
2 |
3 |
1 |
0 |
4 |
2 |
2 |
0 |
3 |
3 |
26 |
| Regulation of intracellular pH in salamander retinal rods | 0 |
1 |
1 |
1 |
4 |
1 |
2 |
2 |
3 |
2 |
3 |
3 |
23 |
| Reproduction under predation risk and the trade-off between current and future reproduction in the threespine stickleback | 0 |
1 |
0 |
0 |
0 |
0 |
1 |
4 |
1 |
3 |
1 |
1 |
12 |
| Reserve Selection Using Nonlinear Species Distribution Models | 1 |
2 |
3 |
5 |
3 |
1 |
3 |
4 |
1 |
6 |
8 |
4 |
41 |
| Resilience and Vulnerability of Northern Regions to Social and Environmental Change | 4 |
1 |
2 |
4 |
2 |
12 |
0 |
3 |
2 |
2 |
5 |
8 |
45 |
| Response univariance in bull-frog rods with two visual pigments | 1 |
3 |
2 |
2 |
2 |
1 |
2 |
2 |
3 |
2 |
1 |
3 |
24 |
| Retinal noise, the performance of retinal ganglion cells, and visual sensitivity in the dark-adapted frog | 0 |
3 |
6 |
4 |
6 |
9 |
5 |
5 |
4 |
2 |
5 |
2 |
51 |
| Retinal origins of the temperature-effect on absolute visual sensitivity in frogs | 2 |
1 |
2 |
2 |
0 |
1 |
2 |
2 |
4 |
4 |
1 |
3 |
24 |
| Returning forests analyzed with the forest identity | 2 |
2 |
4 |
5 |
1 |
4 |
4 |
2 |
3 |
1 |
4 |
1 |
33 |
| Rhodopsin phosphorylation inhibited by adenosine in frog rods : lack of effects on excitation | 0 |
0 |
0 |
1 |
0 |
0 |
1 |
4 |
1 |
0 |
1 |
3 |
11 |
| Road and railway verges serve as dispersal corridors for grassland plants | 0 |
0 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
| Rod phototransduction modulated by bicarbonate in the frog retina : roles of carbonic anhydrase and bicarbonate exchange | 0 |
3 |
2 |
0 |
1 |
0 |
2 |
3 |
1 |
2 |
3 |
1 |
18 |
| Run-Length Compressed Indexes Are Superior for Highly Repetitive Sequence Collections | 1 |
1 |
7 |
0 |
2 |
2 |
0 |
1 |
2 |
1 |
0 |
4 |
21 |
| Satellite image analysis of human caused changes in the tundra vegetation around the city of Vorkuta, north-European Russia | 2 |
1 |
3 |
2 |
7 |
4 |
2 |
2 |
4 |
0 |
1 |
0 |
28 |
| Schwermetallkonzentrationen (Hg, Fe, Mn, Zn, Cd, Pb, und Ni) in Flundern (Platichtys flesus L.) aus der Kieler Förde | 0 |
1 |
2 |
2 |
1 |
0 |
0 |
1 |
0 |
2 |
1 |
1 |
11 |
| Seashore disturbance and management of the clonal Arctophila fulva : Modelling patch dynamics | 2 |
1 |
3 |
3 |
3 |
0 |
1 |
2 |
1 |
3 |
0 |
2 |
21 |
| Seasonal Variations in Cadmium Concentrations of Plant | 1 |
0 |
2 |
1 |
0 |
4 |
0 |
1 |
4 |
4 |
0 |
1 |
18 |
| Selection of Islands for Conservation in the Urban Archipelago of Helsinki, Finland | 4 |
4 |
2 |
3 |
1 |
2 |
1 |
2 |
1 |
0 |
1 |
1 |
22 |
| Selective and reversible control of a chemical reaction with narrow-band infrared radiation : HXeCC radical in solid xenon | 2 |
0 |
2 |
0 |
1 |
1 |
0 |
1 |
0 |
1 |
0 |
1 |
9 |
| Sensitivity Analysis of Discharge in the Arctic Usa Basin East-European Russia | 2 |
0 |
1 |
2 |
0 |
1 |
1 |
13 |
1 |
1 |
1 |
5 |
28 |
| Sensitivity of boreal forests to possible climatic warming. | 0 |
3 |
5 |
9 |
8 |
9 |
4 |
4 |
7 |
3 |
2 |
0 |
54 |
| Sequestering carbon in natural forests | 3 |
3 |
3 |
1 |
2 |
6 |
4 |
3 |
4 |
4 |
4 |
10 |
47 |
| Sevansjön – Transkaukasiens störstä sjö | 0 |
0 |
0 |
2 |
1 |
0 |
1 |
0 |
0 |
0 |
1 |
0 |
5 |
| Shores in the city: opportunities, threaths and challenges : viewpoints of citizens in Helsinki. | 2 |
3 |
3 |
1 |
3 |
0 |
3 |
2 |
4 |
1 |
1 |
0 |
23 |
| Sikiövauriot vaarana, elohopea on ongelma Etelä-Amerikassa | 3 |
1 |
2 |
0 |
3 |
1 |
5 |
4 |
2 |
0 |
3 |
1 |
25 |
| Sinisimpukan (Mytilus edulis L.) raskasmetallipitoisuuksia | 5 |
5 |
5 |
3 |
6 |
7 |
11 |
7 |
2 |
2 |
4 |
4 |
61 |
| Skogarna och koldioxidfrågan | 1 |
0 |
1 |
2 |
0 |
0 |
0 |
0 |
1 |
0 |
2 |
3 |
10 |
| Sorption and Mobilization of Mercury in Peat Soil | 0 |
2 |
4 |
3 |
3 |
2 |
3 |
3 |
4 |
2 |
3 |
1 |
30 |
| Sorption of mercury in soils with different humus content | 8 |
2 |
1 |
3 |
2 |
2 |
4 |
4 |
3 |
5 |
4 |
0 |
38 |
| Space-Efficient String Mining under Frequency Constraints | 0 |
2 |
0 |
5 |
2 |
1 |
0 |
3 |
1 |
0 |
0 |
0 |
14 |
| Spatial ecology of the three-toed woodpecker in managed forest landscapes. | 2 |
4 |
3 |
0 |
1 |
3 |
5 |
5 |
3 |
1 |
0 |
0 |
27 |
| Spatial variation of arthropod communities in virgin and managed sites in the Kibale Forest, western Uganda. | 0 |
0 |
3 |
0 |
2 |
1 |
1 |
1 |
1 |
2 |
1 |
4 |
16 |
| Spawning succession of spring-spawning fishes [Abstract] | 1 |
3 |
2 |
0 |
1 |
5 |
0 |
0 |
2 |
2 |
2 |
0 |
18 |
| Species-level selection reduces selfishness through competitive exclusion. | 0 |
2 |
3 |
0 |
2 |
4 |
1 |
0 |
4 |
3 |
0 |
0 |
19 |
| Specific integrin alpha and beta chain phosphorylations regulate LFA-1 activation through affinity-dependent and -independent mechanisms | 0 |
1 |
1 |
1 |
0 |
1 |
1 |
7 |
1 |
1 |
3 |
2 |
19 |
| Spectral sensitivities of short- and long-wavelength sensitive cone mechanisms in the frog retina | 1 |
3 |
7 |
113 |
13 |
9 |
12 |
5 |
3 |
5 |
7 |
5 |
183 |
| Spånakäringen (Saduria entomon L.) som miljöbioindikator | 0 |
2 |
3 |
3 |
1 |
1 |
4 |
3 |
1 |
0 |
0 |
2 |
20 |
| Stress and Strain in Ecosystems | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
0 |
0 |
1 |
3 |
| Sulfhydryl Binding Reagents Increase the Conductivity of the Light-Sensitive Channel and Inhibit Phototransduction in Retinal Rods | 1 |
2 |
3 |
1 |
3 |
1 |
0 |
2 |
1 |
1 |
2 |
2 |
19 |
| Suomen Akatemia on yliopistolle hidas ja turha | 0 |
1 |
1 |
1 |
5 |
1 |
0 |
1 |
0 |
2 |
1 |
0 |
13 |
| Suomen metsät on myytävä Brysselille | 0 |
2 |
5 |
1 |
3 |
1 |
2 |
1 |
3 |
1 |
3 |
2 |
24 |
| Suomen ympäristöpäästöt vähenivät jo ennen EU-jäsenyyttä | 0 |
1 |
1 |
0 |
0 |
0 |
1 |
1 |
2 |
1 |
0 |
1 |
8 |
| Surround control of center adaptation in the receptive fields of frog retinal ganglion | 1 |
2 |
3 |
1 |
7 |
3 |
4 |
2 |
3 |
1 |
3 |
7 |
37 |
| Taimet uusiin pakkauksiin. | 2 |
3 |
0 |
2 |
2 |
3 |
2 |
0 |
1 |
1 |
2 |
1 |
19 |
| Technological and Economic Potential of Options to Enhance, Maintain, and Manage Biological Carbon Reservoirs and Geo-engineering. | 2 |
1 |
1 |
1 |
7 |
1 |
5 |
5 |
3 |
3 |
3 |
5 |
37 |
| Temperature-dependence of rod photoresponses from the aspartate-treated retina of the frog (Rana temporia) | 2 |
0 |
4 |
5 |
4 |
7 |
5 |
1 |
1 |
1 |
4 |
7 |
41 |
| Testing abundance-range size relationships in European carabid beetles (Coleoptera, Carabidae). | 1 |
1 |
5 |
3 |
4 |
2 |
0 |
1 |
1 |
2 |
1 |
2 |
23 |
| The absolute sensitivity of vision : can a frog become a perfect detector of light-induced and dark rod events? | 3 |
3 |
5 |
5 |
6 |
5 |
3 |
1 |
4 |
4 |
1 |
2 |
42 |
| The climatic impacts of land surface change and carbon management, and the implications for climate-change mitigation policy | 5 |
8 |
9 |
5 |
3 |
5 |
20 |
7 |
1 |
3 |
6 |
2 |
74 |
| The Dynamics of Ecosystems, Biodiversity Management and Social Institutions at High Northern Latitudes | 0 |
4 |
1 |
1 |
5 |
2 |
1 |
0 |
2 |
7 |
7 |
3 |
33 |
| The ecogenetic link between demography and evolution : can we bridge the gap between theory and data? | 10 |
7 |
6 |
4 |
0 |
2 |
3 |
4 |
2 |
0 |
2 |
1 |
41 |
| The Effect of Lead Processing Works on the Lead, Cadmium and Mercury Contents of Fungi. | 1 |
2 |
5 |
5 |
3 |
1 |
2 |
1 |
3 |
3 |
3 |
2 |
31 |
| The effect of metals on the mortality of Parnassius apollo larvae (Lepidoptera: Papilionidae) | 2 |
1 |
5 |
4 |
1 |
1 |
2 |
5 |
4 |
0 |
1 |
2 |
28 |
| The effect of mineralogy, texture and mechanical properties of anti-skid and asphalt aggregates on urban dust | 1 |
3 |
4 |
3 |
1 |
3 |
3 |
9 |
2 |
1 |
3 |
2 |
35 |
| The Effect of Traction Sanding on Urban Suspended Particles in Finland | 0 |
3 |
1 |
2 |
0 |
0 |
0 |
1 |
2 |
0 |
3 |
2 |
14 |
| The effects of simultaneous large acidic and alkaline airborne pollutants on forest soil | 1 |
2 |
3 |
2 |
1 |
2 |
4 |
0 |
4 |
5 |
2 |
2 |
28 |
| The effects of trampling on assemblages of ground beetles (Coleoptera, Carabidae) in urban forests in Helsinki, Finland | 0 |
1 |
0 |
2 |
2 |
3 |
9 |
7 |
4 |
0 |
0 |
6 |
34 |
| The frequency of isomerization-like “dark” events in rhodopsin and porphyropsin rods of the bullfrog retina | 2 |
4 |
0 |
3 |
1 |
2 |
4 |
1 |
4 |
1 |
2 |
1 |
25 |
| The implications of poaching for giant panda conservation | 3 |
0 |
1 |
10 |
8 |
8 |
13 |
23 |
4 |
10 |
13 |
10 |
103 |
| The p-norm generalization of the LMS algorithm for adaptive filtering | 1 |
2 |
3 |
1 |
1 |
1 |
2 |
1 |
1 |
2 |
6 |
2 |
23 |
| The relationship between signal quality and physical condition : is sexual signalling honest in the three-spined stickleback? | 2 |
3 |
2 |
3 |
1 |
1 |
0 |
3 |
5 |
1 |
1 |
1 |
23 |
| The search for common anthropogenic impacts on biodiversity : a global network | 1 |
1 |
4 |
13 |
5 |
4 |
2 |
2 |
8 |
8 |
13 |
7 |
68 |
| The sustainability challenge of meeting carbon dioxide targets in Europe by 2020 | 0 |
0 |
0 |
3 |
1 |
2 |
0 |
0 |
0 |
1 |
1 |
1 |
9 |
| The tragedy of the commons in evolutionary biology. | 30 |
53 |
40 |
35 |
23 |
24 |
21 |
23 |
52 |
35 |
30 |
14 |
380 |
| The United Nations Climate Convention : Unattainable or Irrelevant | 1 |
3 |
4 |
2 |
2 |
1 |
2 |
2 |
0 |
1 |
0 |
0 |
18 |
| The use of multiple cues in mate choice | 19 |
10 |
9 |
24 |
13 |
8 |
8 |
4 |
10 |
1 |
5 |
3 |
114 |
| Thermal Activation and Photoactivation of Visual Pigments | 0 |
0 |
2 |
0 |
1 |
3 |
5 |
6 |
0 |
3 |
2 |
1 |
23 |
| Throughfall monitoring as a means of monitoring deposition to forest ecosystems, evaluation of European Data. | 1 |
3 |
2 |
0 |
3 |
1 |
2 |
2 |
1 |
4 |
2 |
3 |
24 |
| Titicacasjön – Sydamerikas störstä och jordens högst belägna sjö | 0 |
0 |
6 |
0 |
1 |
0 |
2 |
0 |
1 |
0 |
2 |
1 |
13 |
| Top-down approaches for sharing GHG emission reductions : uncertainties and sensitivities in the 27 European Union Member States | 3 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
1 |
0 |
6 |
| Torsken (Gadus morhua L.) i Östersjön | 1 |
1 |
2 |
2 |
3 |
1 |
0 |
4 |
0 |
1 |
2 |
1 |
18 |
| Towards the theory of decoupling : Degrees of decoupling in the EU and the case of road traffic in Finland between 1970 and 2001 | 26 |
16 |
14 |
15 |
27 |
58 |
51 |
81 |
41 |
20 |
26 |
19 |
394 |
| Transient sensitivity reduction and biphasic photoresponses observed when retinal rods are oxidized | 1 |
0 |
0 |
0 |
1 |
1 |
2 |
1 |
0 |
0 |
0 |
0 |
6 |
| Trees as carbon sinks and sources in the European Union | 12 |
3 |
3 |
1 |
3 |
1 |
12 |
4 |
2 |
6 |
2 |
1 |
50 |
| Tungmetaller i den marina Tvärminnemiljön | 3 |
4 |
1 |
1 |
0 |
0 |
3 |
1 |
1 |
3 |
0 |
2 |
19 |
| Tutkimusrahoitus otettava yliopistouudistuksen asialistalle | 1 |
1 |
2 |
0 |
0 |
0 |
0 |
4 |
0 |
0 |
0 |
2 |
10 |
| Tvärminne rakkolevä (Fucus vesiculosus L.) ympäristön tilan kuvaajana | 1 |
1 |
0 |
0 |
4 |
5 |
2 |
2 |
1 |
1 |
0 |
5 |
22 |
| Tvärminnefiskens kvicksilverhalter | 0 |
0 |
0 |
1 |
1 |
0 |
4 |
0 |
0 |
1 |
0 |
0 |
7 |
| Tvärminnemusslorna Macoma balthica L. och Mytilus edulis L., som miljöbioindikatorer | 0 |
2 |
1 |
0 |
3 |
0 |
4 |
2 |
1 |
0 |
3 |
2 |
18 |
| Tvärminnen alueen eräiden pohjapintasedimaenttien ja pohjaeläinten raskasmetallipitoisuuksia | 0 |
0 |
2 |
1 |
1 |
1 |
0 |
2 |
0 |
0 |
2 |
0 |
9 |
| Tånglaken i våra skärgårdsvatten | 0 |
2 |
1 |
2 |
0 |
5 |
4 |
1 |
2 |
2 |
1 |
2 |
22 |
| Vesien tilaan myönteisesti ja kielteisesti vaikuttavat valtiovallan tukitoimet | 5 |
6 |
5 |
8 |
4 |
7 |
4 |
10 |
2 |
4 |
5 |
5 |
65 |
| Vetenskap av allmänfattlig art | 1 |
1 |
2 |
1 |
2 |
0 |
1 |
2 |
2 |
1 |
2 |
0 |
15 |
| Vibrational coordinates and their gradients : A geometric algebra approach | 2 |
1 |
3 |
2 |
2 |
4 |
3 |
4 |
1 |
1 |
2 |
3 |
28 |
| Vibration–rotation kinetic energy operators : A geometric algebra approach | 1 |
2 |
5 |
1 |
0 |
0 |
0 |
2 |
2 |
0 |
0 |
0 |
13 |
| Visual latency and brightness : an interpretation based on the responses of rods and ganglion cells in the frog retina | 0 |
6 |
1 |
2 |
2 |
6 |
7 |
2 |
2 |
2 |
2 |
1 |
33 |
| Visual performance of the toad (bufo bufo) at low light levels : Retinal ganglion cell responses and prey-catching accuracy | 2 |
3 |
8 |
7 |
7 |
6 |
4 |
2 |
2 |
2 |
3 |
1 |
47 |
| Volatilisation of Heavy Metals from a Refuse Dump | 0 |
3 |
2 |
2 |
2 |
3 |
0 |
12 |
0 |
1 |
4 |
3 |
32 |
| Väitöslektio 18.1.1985 | 4 |
2 |
2 |
2 |
0 |
5 |
2 |
1 |
0 |
1 |
2 |
0 |
21 |
| Water Hyacinth as Indicator of Heavy Metal Pollution in the Tropics. | 1 |
2 |
7 |
9 |
1 |
2 |
7 |
24 |
4 |
6 |
1 |
2 |
66 |
| Water Quality and Fish in two Freshwater Reservoirs (Gennarby and Sysilax) on the SW Coast of Finland | 2 |
3 |
2 |
5 |
1 |
5 |
3 |
4 |
4 |
3 |
4 |
3 |
39 |
| Water Striders (Heteroptera Gerridae) as bioindicators of heavy metal pollution | 2 |
4 |
0 |
3 |
3 |
2 |
1 |
1 |
1 |
2 |
3 |
2 |
24 |
| Weber and Noise Adaptation in the Retina of the Toad Bufo marinus | 0 |
0 |
1 |
1 |
3 |
2 |
4 |
1 |
2 |
1 |
3 |
1 |
19 |
| What determines sex roles in mate searching? | 1 |
1 |
2 |
0 |
0 |
0 |
3 |
0 |
2 |
0 |
1 |
0 |
10 |
| Wind power in Finland up to the year 2025 : ‘soft’ scenarios based on expert views | 0 |
0 |
1 |
1 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
3 |
6 |
| Wood supply and carbon sequestration: situation and changes : B: Carbon cycle and biomass. | 0 |
1 |
8 |
2 |
4 |
0 |
4 |
3 |
0 |
2 |
2 |
2 |
28 |
| Year-to-year variation in carabid beetle (Coleoptera, Carabidae) assemblages on the Åland Islands, south-west Finland | 2 |
3 |
3 |
1 |
7 |
7 |
8 |
29 |
1 |
2 |
1 |
0 |
64 |
| Ympäristötieteen professori Pekka Kauppi : metsävarat lisääntyneet merkittävästi | 0 |
2 |
4 |
5 |
2 |
4 |
2 |
7 |
2 |
3 |
3 |
3 |
37 |
| Ytterligare ett fall av blomkålssjuka hos ål | 1 |
4 |
2 |
2 |
3 |
0 |
0 |
1 |
0 |
0 |
3 |
1 |
17 |
| Öring och röding i reglerade sjöar : ny syn på fiskodlingen | 2 |
2 |
5 |
6 |
0 |
0 |
3 |
2 |
1 |
2 |
2 |
1 |
26 |
| Österjöns och våra insjöars utveckling | 0 |
2 |
1 |
2 |
1 |
0 |
1 |
0 |
1 |
0 |
1 |
1 |
10 |
| Östersjöströmmingen och miljögifterna | 0 |
1 |
0 |
1 |
0 |
0 |
0 |
1 |
0 |
2 |
2 |
2 |
9 |