| Why we love bees and hate wasps |
16 |
| The tethered flight technique as a tool for studying life-history strategies associated with migration in insects |
13 |
| Competition between the native and the introduced hornets Vespa crabro and Vespa velutina: a comparison of potentially relevant life-history traits |
13 |
| Construction, validation, and application of nocturnal pollen transport networks in an agro-ecosystem: a comparison using light microscopy and DNA metabarcoding |
12 |
| Transgenerational developmental effects of species-specific, maternally transmitted microbiota in Onthophagus dung beetles |
11 |
| Nature protection areas of Europe are insufficient to preserve the threatened beetle Rosalia alpina (Coleoptera: Cerambycidae): evidence from species distribution models and conservation gap analysis |
11 |
| Mechanisms structuring host-parasitoid networks in a global warming context: a review |
11 |
| The impacts of predators and parasites on wild bumblebee colonies |
10 |
| Secondary seed dispersal by ants in Neotropical cerrado savanna: species-specific effects on seeds and seedlings of Siparuna guianensis (Siparunaceae) |
9 |
| Are all urban green spaces a favourable habitat for pollinator communities? Bees, butterflies and hoverflies in different urban green areas |
9 |
| The role of temperature in competition and persistence of an invaded ant assemblage |
8 |
| Dung beetle diversity and functions suggest no major impacts of cattle grazing in the Brazilian Pantanal wetlands |
8 |
| Extreme ecological stoichiometry of a bark beetle-fungus mutualism |
8 |
| Male pheromone composition depends on larval but not adult diet in Heliconius melpomene |
7 |
| Lower thermal tolerance in nocturnal than in diurnal ants: a challenge for nocturnal ectotherms facing global warming |
7 |
| Experimental warming disrupts reproduction and dung burial by a ball-rolling dung beetle |
6 |
| Not berry hungry? Discovering the hidden food sources of a small fruit specialist, Drosophila suzukii |
6 |
| Shrub shading moderates the effects of weather on arthropod activity in arctic tundra |
6 |
| An interspecific test of Bergmann's rule reveals inconsistent body size patterns across several lineages of water beetles (Coleoptera: Dytiscidae) |
6 |
| Different predation efficiencies of trap-building larvae of sympatric antlions and wormlions from the rainforest of Borneo |
6 |
| Mean body size predicts colony performance in the common eastern bumble bee (Bombus impatiens) |
6 |
| Inferring origins of migrating insects using isoscapes: a case study using the true armyworm, Mythimna unipuncta, in North America |
6 |
| A temperate pollinator with high thermal tolerance is still susceptible to heat events predicted under future climate change |
5 |
| Soil surface complexity has a larger effect on food exploitation by ants than a change from grassland to shrubland |
5 |
| Fruit-breeding drosophilids (Diptera) in the Neotropics: playing the field and specialising in generalism? |
5 |
| Drosophila melanogaster infected with Wolbachia strain wMelCS prefer cooler temperatures |
5 |
| Field experiments show contradictory short- and long-term myrmecochorous plant impacts on seed-dispersing ants |
4 |
| Asymmetric effects of a leaf-chewing herbivore on aphid population growth |
4 |
| Spatial synchrony in Drosophila suzukii population dynamics along elevational gradients |
4 |
| Distinct feeding strategies of generalist and specialist spiders |
4 |
| Takeoff temperatures in Melitaea cinxia butterflies from latitudinal and elevational range limits: a potential adaptation to solar irradiance |
4 |
| The forgotten season: the impact of autumn phenology on a specialist insect herbivore community on oak |
4 |
| Trophic ecology of adult male Odonata. I. Dietary niche metrics by foraging guild, species, body size, and location |
4 |
| Structural changes over time in individual-based networks involving a harvester ant, seeds, and invertebrates |
4 |
| Plant composition, not richness, drives occurrence of specialist herbivores |
4 |
| Negative spatial covariation in abundance of two European ticks: diverging niche preferences or biotic interaction? |
4 |
| Nesting aggregation as a predictor of brood parasitism in mason bees (Osmia spp.) |
4 |
| Relative importance of drought, soil quality, and plant species in determining the strength of plant-herbivore interactions |
4 |
| The responses of wild jacamars (Galbula ruficauda, Galbulidae) to aposematic, aposematic and cryptic, and cryptic butterflies in central Brazil |
4 |
| Separation between maternal and paternal effects on offspring following exposure of adult red flour beetles to two stressors |
4 |
| Substrate moisture, particle size and temperature preferences of trap-building larvae of sympatric antlions and wormlions from the rainforest of Borneo |
4 |
| Termitariophily: expanding the concept of termitophily in a physogastric rove beetle (Coleoptera: Staphylinidae) |
4 |
| Fire? They don't give a dung! The resilience of dung beetles to fire in a tropical savanna |
4 |
| Cold hardiness of Lymantria monacha and L-dispar (Lepidoptera: Erebidae) eggs to extreme winter temperatures: implications for predicting climate change impacts |
3 |
| The role of biofoam in shielding spittlebug nymphs (Insecta, Hemiptera, Cercopidae) against bright light |
3 |
| Coexistence between two fruit fly species is supported by the different strength of intra- and interspecific competition |
3 |
| Resource density regulates the foraging investment in higher termite species |
3 |
| Fitness and microbial networks of the common wasp, Vespula vulgaris (Hymenoptera: Vespidae), in its native and introduced ranges |
3 |
| Biotic and abiotic determinants of the formation of ant mosaics in primary Neotropical rainforests |
3 |
| Spatial and temporal diversity in hyperparasitoid communities of Cotesia glomerata on garlic mustard, Alliaria petiolata |
3 |
