| 1 | A new index to estimate ecological generalisation in consumer‐resource interactions | 5.2 | 1 | Citations (PDF) |
| 2 | Risk response towards roads is consistent across multiple species in a temperate forest ecosystem | 2.6 | 5 | Citations (PDF) |
| 3 | The importance of temporal scale in distribution modeling of migratory Caspian Kutum, <i>Rutilus frisii</i> | 2.0 | 4 | Citations (PDF) |
| 4 | Exotic tree species have consistently lower herbivore load in a cross‐<scp>A</scp>tlantic tree biodiversity experiment | 3.3 | 11 | Citations (PDF) |
| 5 | Why we need a Canonical Ecology Curriculum | 3.3 | 3 | Citations (PDF) |
| 6 | Numerical top‐down effects on red deer (<i>Cervus elaphus</i>) are mainly shaped by humans rather than large carnivores across Europe | 3.8 | 21 | Citations (PDF) |
| 7 | Quantitative Prediction of Interactions in Bipartite Networks Based on Traits, Abundances, and Phylogeny | 2.4 | 17 | Citations (PDF) |
| 8 | Population density estimates for terrestrial mammal species | 5.5 | 49 | Citations (PDF) |
| 9 | A systematic map of demographic data from elephant populations throughout Africa: implications for poaching and population analyses | 4.0 | 5 | Citations (PDF) |
| 10 | Spatially autocorrelated training and validation samples inflate performance assessment of convolutional neural networks | 3.6 | 66 | Citations (PDF) |
| 11 | Habitat diversity and peat moss cover drive the occurrence probability of the threatened ground beetle Carabus menetriesi (Coleoptera: Carabidae) in a Bavarian mire | 1.7 | 0 | Citations (PDF) |
| 12 | Seeing through the static: the temporal dimension of plant–animal mutualistic interactions | 11.2 | 108 | Citations (PDF) |
| 13 | Tree diversity reduces the risk of bark beetle infestation for preferred conifer species, but increases the risk for less preferred hosts | 4.6 | 40 | Citations (PDF) |
| 14 | Curvature of Logs—Development of and Comparison between Different Calculation Approaches | 2.3 | 3 | Citations (PDF) |
| 15 | Within-day dynamics of plant–pollinator networks are dominated by early flower closure: an experimental test of network plasticity | 1.7 | 20 | Citations (PDF) |
| 16 | European agroforestry has no unequivocal effect on biodiversity: a time-cumulative meta-analysis | 1.9 | 36 | Citations (PDF) |
| 17 | Humpback whales extend their stay in a breeding ground in the Tropical Eastern Pacific | 2.8 | 35 | Citations (PDF) |
| 18 | Insect abundance in managed forests benefits from multi-layered vegetation | 3.3 | 62 | Citations (PDF) |
| 19 | Plant species richness increases with light availability, but not variability, in temperate forests understorey | 3.4 | 133 | Citations (PDF) |
| 20 | Exploration of Concerns about the Evidence-Based Guideline Approach in Conservation Management: Hints from Medical Practice | 2.4 | 12 | Citations (PDF) |
| 21 | Spatial validation reveals poor predictive performance of large-scale ecological mapping models | 13.9 | 462 | Citations (PDF) |
| 22 | Temporal scale‐dependence of plant–pollinator networksOikos, 2020, 129, 1289-1302 | 2.6 | 95 | Citations (PDF) |
| 23 | A standard protocol for reporting species distribution models | 4.7 | 747 | Citations (PDF) |
| 24 | Spatial conservation prioritisation in data-poor countries: a quantitative sensitivity analysis using multiple taxa | 3.4 | 13 | Citations (PDF) |
| 25 | Co-occurrence patterns and the large-scale spatial structure of benthic communities in seagrass meadows and bare sand | 3.4 | 8 | Citations (PDF) |
| 26 | The influence of camera trap flash type on the behavioural reactions and trapping rates of red deer and roe deer | 4.4 | 20 | Citations (PDF) |
| 27 | Evaluating the effectiveness of retention forestry to enhance biodiversity in production forests of Central Europe using an interdisciplinary, multi‐scale approach | 2.0 | 82 | Citations (PDF) |
| 28 | Calibration of probability predictions from machine‐learning and statistical models | 5.5 | 40 | Citations (PDF) |
| 29 | Increasing connectivity enhances habitat specialists but simplifies plant–insect food webs | 1.7 | 15 | Citations (PDF) |
| 30 | Breaking the ecosystem services glass ceiling: realising impact | 3.2 | 6 | Citations (PDF) |
| 31 | Spatial behavior in rehabilitated orangutans in Sumatra: Where do they go? | 2.4 | 3 | Citations (PDF) |
| 32 | A new model explaining the origin of different topologies in interaction networks | 3.3 | 56 | Citations (PDF) |
| 33 | African elephant poaching rates correlate with local poverty, national corruption and global ivory price | 13.9 | 83 | Citations (PDF) |
| 34 | Refuges from fire maintain pollinator–plant interaction networks | 2.0 | 36 | Citations (PDF) |
| 35 | Does Public Participation Shift German National Park Priorities Away from Nature Conservation? | 1.7 | 18 | Citations (PDF) |
| 36 | Blind spots in ecosystem services research and challenges for implementation | 3.2 | 100 | Citations (PDF) |
| 37 | Standards for distribution models in biodiversity assessments | 11.0 | 938 | Citations (PDF) |
| 38 | Forest-edge associated bees benefit from the proportion of tropical forest regardless of its edge length | 3.7 | 39 | Citations (PDF) |
| 39 | Current global risks to marine mammals: Taking stock of the threats | 3.7 | 277 | Citations (PDF) |
| 40 | Consistent set of additive biomass functions for eight tree species in Germany fit by nonlinear seemingly unrelated regression | 2.2 | 28 | Citations (PDF) |
| 41 | Disturbance intensity is a stronger driver of biomass recovery than remaining tree‐community attributes in a managed Amazonian forest | 3.8 | 40 | Citations (PDF) |
| 42 | Wrong, but useful: regional species distribution models may not be improved by range‐wide data under biased sampling | 2.0 | 78 | Citations (PDF) |
| 43 | Modelling the variation of bark thickness within and between European silver fir (Abies alba Mill.) trees in southwest Germany | 2.3 | 24 | Citations (PDF) |
| 44 | Model averaging in ecology: a review of Bayesian, information‐theoretic, and tactical approaches for predictive inference | 8.4 | 338 | Citations (PDF) |
| 45 | Computing AIC for black-box models using generalized degrees of freedom: A comparison with cross-validation | 1.4 | 18 | Citations (PDF) |
| 46 | An efficient method to exploit Li<scp>DAR</scp> data in animal ecology | 5.2 | 33 | Citations (PDF) |
| 47 | Quantifying forest structural diversity based on large-scale inventory data: a new approach to support biodiversity monitoring | 4.0 | 90 | Citations (PDF) |
| 48 | Improved species‐occurrence predictions in data‐poor regions: using large‐scale data and bias correction with down‐weighted Poisson regression and Maxent | 4.7 | 69 | Citations (PDF) |
| 49 | Crop pests and predators exhibit inconsistent responses to surrounding landscape composition | 7.6 | 519 | Citations (PDF) |
| 50 | Biotic interactions in species distribution modelling: 10 questions to guide interpretation and avoid false conclusions | 5.5 | 280 | Citations (PDF) |
| 51 | Decaying trees improve nesting opportunities for cavity‐nesting birds in temperate and boreal forests: A meta‐analysis and implications for retention forestry | 2.0 | 59 | Citations (PDF) |
| 52 | Outstanding Challenges in the Transferability of Ecological Models | 7.6 | 612 | Citations (PDF) |
| 53 | Fragmentation of nest and foraging habitat affects time budgets of solitary bees, their fitness and pollination services, depending on traits: Results from an individual-based model | 2.4 | 63 | Citations (PDF) |
| 54 | Comparison of models for estimating bark thickness of Picea abies in southwest Germany: the role of tree, stand, and environmental factors | 2.2 | 29 | Citations (PDF) |
| 55 | Cross‐validation strategies for data with temporal, spatial, hierarchical, or phylogenetic structure | 4.7 | 1,803 | Citations (PDF) |
| 56 | Recruitment, growth and recovery of commercial tree species over 30 years following logging and thinning in a tropical rain forest | 3.7 | 87 | Citations (PDF) |
| 57 | Identifying Causes of Patterns in Ecological Networks: Opportunities and Limitations | 8.8 | 202 | Citations (PDF) |
| 58 | No consistent effect of plant species richness on resistance to simulated climate change for above- or below-ground processes in managed grasslands | 3.4 | 11 | Citations (PDF) |
| 59 | Influence of Forest Harvest on Nitrate Concentration in Temperate Streams—A Meta-Analysis | 2.3 | 22 | Citations (PDF) |
| 60 | The former Iron Curtain still drives biodiversity–profit trade-offs in German agriculture | 10.3 | 159 | Citations (PDF) |
| 61 | An evidence assessment tool for ecosystem services and conservation studies | 3.9 | 57 | Citations (PDF) |
| 62 | Ecological networks are more sensitive to plant than to animal extinction under climate change | 13.9 | 227 | Citations (PDF) |
| 63 | Detection probabilities for sessile organisms | 2.6 | 19 | Citations (PDF) |
| 64 | Squares of different sizes: effect of geographical projection on model parameter estimates in species distribution modeling | 2.0 | 21 | Citations (PDF) |
| 65 | The influence of floral traits on specialization and modularity of plant–pollinator networks in a biodiversity hotspot in the Peruvian Andes | 3.1 | 95 | Citations (PDF) |
| 66 | Effectiveness of light-reflecting devices: A systematic reanalysis of animal-vehicle collision data | 5.5 | 24 | Citations (PDF) |
| 67 | Measurement and prediction of bark thickness in <i>Picea abies</i>: assessment of accuracy, precision, and sample size requirements | 1.8 | 27 | Citations (PDF) |
| 68 | Dispersal Ecology Informs Design of Large-Scale Wildlife Corridors | 2.4 | 30 | Citations (PDF) |
| 69 | Medium-term dynamics of tree species composition in response to silvicultural intervention intensities in a tropical rain forest | 3.7 | 65 | Citations (PDF) |
| 70 | Effects of warming and drought on potential N<sub>2</sub>O emissions and denitrifying bacteria abundance in grasslands with different land-use | 2.8 | 46 | Citations (PDF) |
| 71 | Community structure and ecological specialization in plant–ant interactions | 1.0 | 6 | Citations (PDF) |
| 72 | Cross-Scale Variation in Biodiversity-Environment Links Illustrated by Coastal Sandflat Communities | 2.4 | 20 | Citations (PDF) |
| 73 | Interannual variation in land-use intensity enhances grassland multidiversity | 7.6 | 325 | Citations (PDF) |
| 74 | The<scp>PREDICTS</scp>database: a global database of how local terrestrial biodiversity responds to human impacts | 2.0 | 221 | Citations (PDF) |
| 75 | Stacking species distribution models and adjusting bias by linking them to macroecological models | 5.5 | 334 | Citations (PDF) |
| 76 | Choices of abundance currency, community definition and diversity metric control the predictive power of macroecological models of biodiversity | 5.5 | 8 | Citations (PDF) |
| 77 | Accounting for geographical variation in species–area relationships improves the prediction of plant species richness at the global scale | 3.2 | 51 | Citations (PDF) |
| 78 | EDITOR'S CHOICE: REVIEW: Effects of land use on plant diversity – A global meta‐analysis | 3.8 | 106 | Citations (PDF) |
| 79 | A method for detecting modules in quantitative bipartite networks | 5.2 | 514 | Citations (PDF) |
| 80 | Collinearity: a review of methods to deal with it and a simulation study evaluating their performance | 4.7 | 8,650 | Citations (PDF) |
| 81 | Temporal variability of ecological niches: a study on intertidal macrobenthic faunaOikos, 2013, 122, 754-760 | 2.6 | 15 | Citations (PDF) |
| 82 | Bee diversity effects on pollination depend on functional complementarity and niche shifts | 3.3 | 286 | Citations (PDF) |
| 83 | The role of biotic interactions in shaping distributions and realised assemblages of species: implications for species distribution modelling | 11.5 | 1,485 | Citations (PDF) |
| 84 | Organic Farming Favours Insect-Pollinated over Non-Insect Pollinated Forbs in Meadows and Wheat Fields | 2.4 | 30 | Citations (PDF) |
| 85 | “Mind the gap!” – How well does Natura 2000 cover species of European interest? | 1.3 | 70 | Citations (PDF) |
| 86 | Predator richness increases the effect of prey diversity on prey yield | 13.9 | 142 | Citations (PDF) |
| 87 | Landscape moderation of biodiversity patterns and processes ‐ eight hypotheses | 11.5 | 1,755 | Citations (PDF) |
| 88 | Mapping water quality-related ecosystem services: concepts and applications for nitrogen retention and pesticide risk reduction | 8.0 | 21 | Citations (PDF) |
| 89 | Spatial and Temporal Trends of Global Pollination Benefit | 2.4 | 337 | Citations (PDF) |
| 90 | Spillover of functionally important organisms between managed and natural habitats | 6.4 | 515 | Citations (PDF) |
| 91 | The responses of grassland plants to experimentally simulated climate change depend on land use and region | 11.1 | 46 | Citations (PDF) |
| 92 | A quantitative index of land-use intensity in grasslands: Integrating mowing, grazing and fertilization | 3.3 | 426 | Citations (PDF) |
| 93 | What's on the horizon for macroecology? | 4.7 | 186 | Citations (PDF) |
| 94 | Mass-flowering crops enhance wild bee abundance | 1.7 | 206 | Citations (PDF) |
| 95 | Landscape elements as potential barriers and corridors for bees, wasps and parasitoids | 3.7 | 119 | Citations (PDF) |
| 96 | Microsite conditions dominate habitat selection of the red mason bee (Osmia bicornis, Hymenoptera: Megachilidae) in an urban environment: A case study from Leipzig, Germany | 9.0 | 63 | Citations (PDF) |
| 97 | Species abundance distributions and richness estimations in fungal metagenomics - lessons learned from community ecology | 3.7 | 166 | Citations (PDF) |
| 98 | Set-aside management: How do succession, sowing patterns and landscape context affect biodiversity? | 6.4 | 127 | Citations (PDF) |
| 99 | On managing the red mason bee (Osmia bicornis) in apple orchards | 1.9 | 88 | Citations (PDF) |
| 100 | Food web structure and biocontrol in a four-trophic level system across a landscape complexity gradient | 2.4 | 126 | Citations (PDF) |
| 101 | Expansion of mass-flowering crops leads to transient pollinator dilution and reduced wild plant pollination | 2.4 | 233 | Citations (PDF) |
| 102 | Reassessing Neotropical angiosperm distribution patterns based on monographic data: a geometric interpolation approach | 2.3 | 17 | Citations (PDF) |
| 103 | TaqMan Real-Time PCR Assays To Assess Arbuscular Mycorrhizal Responses to Field Manipulation of Grassland Biodiversity: Effects of Soil Characteristics, Plant Species Richness, and Functional Traits | 3.5 | 79 | Citations (PDF) |
| 104 | Evolution of climate niches in European mammals? | 2.5 | 59 | Citations (PDF) |
| 105 | Crop–noncrop spillover: arable fields affect trophic interactions on wild plants in surrounding habitats | 1.7 | 34 | Citations (PDF) |
| 106 | Review: Ecological networks – beyond food webs | 3.0 | 839 | Citations (PDF) |
| 107 | Static species distribution models in dynamically changing systems: how good can predictions really be? | 4.7 | 133 | Citations (PDF) |
| 108 | Response to Comment on “Methods to account for spatial autocorrelation in the analysis of species distributional data: a review” | 4.7 | 31 | Citations (PDF) |
| 109 | Indices, Graphs and Null Models: Analyzing Bipartite Ecological Networks | 4.0 | 1,534 | Citations (PDF) |
| 110 | Application of species richness estimators for the assessment of fungal diversity | 1.9 | 66 | Citations (PDF) |
| 111 | Prediction uncertainty of environmental change effects on temperate European biodiversity | 11.2 | 88 | Citations (PDF) |
| 112 | COMPONENTS OF UNCERTAINTY IN SPECIES DISTRIBUTION ANALYSIS: A CASE STUDY OF THE GREAT GREY SHRIKE | 3.3 | 191 | Citations (PDF) |
| 113 | Methods to account for spatial autocorrelation in the analysis of species distributional data: a review | 4.7 | 2,865 | Citations (PDF) |
| 114 | Effects of incorporating spatial autocorrelation into the analysis of species distribution data | 5.5 | 552 | Citations (PDF) |
| 115 | Effects of landscape structure and land‐use intensity on similarity of plant and animal communities | 5.5 | 170 | Citations (PDF) |
| 116 | Promising the future? Global change projections of species distributions | 3.3 | 431 | Citations (PDF) |
| 117 | Assessing the validity of autologistic regression | 2.9 | 113 | Citations (PDF) |
| 118 | Occurrence pattern of Pararge aegeria (Lepidoptera: Nymphalidae) with respect to local habitat suitability, climate and landscape structure | 2.8 | 19 | Citations (PDF) |
| 119 | Competition hierarchy, transitivity and additivity: investigating the effect of fertilisation on plant–plant interactions using three common bryophytes | 1.3 | 13 | Citations (PDF) |
| 120 | Experimental evidence rejects pairwise modelling approach to coexistence in plant communities | 2.4 | 61 | Citations (PDF) |
| 121 | Neighbour identity modifies effects of elevated temperature on plant performance in the High Arctic | 11.1 | 37 | Citations (PDF) |
| 122 | Consequences of manipulations in carbon and nitrogen supply for concentration of anti-herbivore defence compounds in<i><b>Salix polaris</b></i> | 1.4 | 29 | Citations (PDF) |
| 123 | Facilitation and competition in the high Arctic: the importance of the experimental approach | 1.3 | 51 | Citations (PDF) |
| 124 | No evidence for adaptation of two Polygonum viviparum morphotypes of different bulbil characteristics to length of growing season: abundance, biomass and germination | 1.2 | 15 | Citations (PDF) |
| 125 | Flowering, growth and defence in the two sexes: consequences of herbivore exclusion for Salix polaris | 4.1 | 26 | Citations (PDF) |
| 126 | Optimal anti-herbivore defence allocation in Salix polaris: doing it the arctic way? | 0.7 | 2 | Citations (PDF) |
| 127 | Competition and herbivory during salt marsh succession: the importance of forb growth strategy | 4.6 | 57 | Citations (PDF) |