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| Q56753692 | A novel parasitoid and a declining butterfly: cause or coincidence? |
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| Q113798261 | A photographic technique for tracking herbivory on individual leaves through time |
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| Q112800865 | A practical guide to DNA metabarcoding for entomological ecologists |
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| Q57409679 | A trans-national monarch butterfly population model and implications for regional conservation priorities |
| Q113798257 | A variable insect–plant interaction: the relationship between tree budburst phenology and population levels of insect herbivores among trees |
| Q114081941 | A winner in the Anthropocene: changing host plant distribution explains geographical range expansion in the gulf fritillary butterfly |
| Q113173202 | Ability of ovipositing Callosobruchus maculatus females to discriminate between seeds bearing their own eggs and those bearing eggs of other females |
| Q113173207 | Ability of ovipositing seed beetles to discriminate between seeds with differing egg loads |
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| Q56998877 | Aboveground herbivory affects indirect defences of brassicaceous plants against the root feeder Delia radicum Linnaeus: laboratory and field evidence |
| Q57229224 | Absence of intraspecific interference during feeding by the predatory ladybirds Chilocorus spp. (Coleoptera: Coccinellidae) |
| Q113033937 | Absence of wing polymorphism in the arboreal, phytophagous species of some taxa of temperate Hemiptera: an hypothesis |
| Q115396467 | Abundance and diversity of Homoptera in the canopy of a tropical forest |
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| Q113173212 | Abundance and survival of a seed-infesting weevil, Pseudanthonomus hamamelidis (Coleoptera: Curculionidae), on its variable-fruiting host plant, witch-hazel (Hamamelis virginiana) |
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| Q60148110 | Acorn preference under field and laboratory conditions by two flightless Iberian dung beetle species (Thorectes baraudi and Jekelius nitidus): implications for recruitment and management of oak forests in central Spain |
| Q60148141 | Acorn removal and dispersal by the dung beetle Thorectes lusitanicus: ecological implications |
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| Q123180411 | Adaptative significance of a temperature induced diapause in a cosmopolitan parasitoid of Drosophila |
| Q115531820 | Adaptive change in protective coloration in adult striated shieldbugs Graphosoma lineatum (Heteroptera: Pentatomidae): test of detectability of two colour forms by avian predators |
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| Q113798255 | Adjacent trophic-level effects on spatial density dependence in a herbivore—predator—parasitoid system |
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| Q56926918 | Advantages of multiple foundress colonies in Belonogaster juncea juncea L.: greater survival and increased productivity |
| Q129577929 | Aerial dispersal ability does not drive spider success in a crop landscape |
| Q126214784 | Aestivation as a response to climate change: the Great Banded Grayling Brintesia circe in Central Europe |
| Q115532224 | Age and experience influence patch assessment for oviposition by an insect predator |
| Q57032295 | Age-dependent clutch size in a koinobiont parasitoid |
| Q56771585 | Age-related cannibalism and horizontal transmission of a nuclear polyhedrosis virus in larval Spodoptera frugiperda |
| Q56228188 | Age-specific maternal effects interact with larval food supply to modulate life history inColeomegilla maculata |
| Q56753966 | Aggregative oviposition of a phytophagous beetle overcomes egg-crushing plant defences |
| Q112800875 | Agri-environmental schemes affect the trophic niche size and diet of common carabid species in agricultural landscapes |
| Q115208873 | Agro-ecosystem services and dis-services in almond orchards are differentially influenced by the surrounding landscape |
| Q57648931 | Alate production in an aphid in relation to ant tending and alarm pheromone |
| Q60567852 | Alien herbivores and native parasitoids: rapid developments and structure of the parasitoid and inquiline complex in an invading gall wasp Andricus quercuscalicis (Hymenoptera: Cynipidae) |
| Q61762050 | Allee effect in larval resource exploitation in Drosophila: an interaction among density of adults, larvae, and micro-organisms |
| Q112798583 | Allometry between leg and body length of insects: lack of support for the size-grain hypothesis |
| Q117787916 | Allopatric populations of the invasive larch casebearer differ in cold tolerance and phenology |
| Q115396440 | Alternative reproductive routines in a small fly, Puliciphora borinquenensis (Diptera: Phoridae) |
| Q59848442 | Alternative seed defence mechanisms in a palo verde (Fabaceae) hybrid zone: effects on bruchid beetle abundance |
| Q37010154 | Amino acid sources in the adult diet do not affect life span and fecundity in the fruit-feeding butterfly Bicyclus anynana |
| Q115396428 | An alternative mating system in small male insects |
| Q54646980 | An analysis of the nesting behaviour of Geotrupes spiniger Marsham (Coleoptera, Scarabaeidae) |
| Q111263889 | An ant—treehopper mutualism: effects of Formica subsericea on the survival of Vanduzea arquata |
| Q56853189 | An economic model of the limits to foraging range in central place foragers with numerical solutions for bumblebees |
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| Q124791705 | An experimental examination of the effects of habitat quality on the dispersal and local abundance of the butterfly Parnassius smintheus |
| Q57228413 | Analysing plant-pollinator interactions with spatial movement networks |
| Q129674408 | Analysing the effect of ivermectin on the volatile organic compounds of dung and its possible influence on attraction to dung beetles |
| Q113798269 | Annual respiration and production estimates for collembolan and psocopteran epiphyte herbivores on larch trees in southern England |
| Q112798597 | Another look at prey detection by coccinellids |
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| Q125967173 | Ant attendance in aphids: why different degrees of myrmecophily? |
| Q115396375 | Ant biodiversity and the predatory function (A response to Philpott and Armbrecht, 2006) |
| Q111263907 | Ant mutualists alter the composition and attack rate of the parasitoid community for the gall wasp Disholcaspis eldoradensis (Cynipidae) |
| Q115405380 | Ant nest distribution and richness have opposite effects on a Neotropical plant with extrafloral nectaries |
| Q111172596 | Ant preference for seeds without awns increases removal of exotic relative to native grass seeds |
| Q113174524 | Ant species but not trait diversity increases at the edges: insights from a micro‐scale gradient in a semi‐natural Mediterranean ecosystem |
| Q59118170 | Ant species distribution in a sandy coastal plain |
| Q56942163 | Ant versus bird exclusion effects on the arthropod assemblage of an organic citrus grove |
| Q57052485 | Ants impact the energy reserves of natural enemies through the shared honeydew exploitation |
| Q60438849 | Aphid and host-plant genotype × genotype interactions under elevated CO2 |
| Q111591533 | Aphid population dynamics: does resistance to parasitism influence population size? |
| Q60317072 | Apparent competition leaves no detectable imprint on patterns of community composition: observations from a natural experiment |
| Q58831375 | Application of r/K selection to macroinvertebrate responses to extreme floods |
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| Q127405869 | Are ants botanists? Ant associative learning of plant chemicals mediates foraging for carbohydrates |
| Q56880096 | Are behavioural responses to predation cues linked across life cycle stages? |
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| Q58740124 | Are the spatio-temporal dynamics of soil-feeding termite colonies shaped by intra-specific competition? |
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| Q115532899 | Arthropod carrion influences plant choice, oviposition, and cannibalism by a specialist predator on a sticky plant |
| Q115396371 | Arthropod community diversity and trophic structure: a comparison between extremes of plant stress |
| Q126032166 | Arthropod ecosystem services in apple orchards and their economic benefits |
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| Q125906592 | Assessing the density of honey bee colonies at ecosystem scales |
| Q56980708 | Assessing the role of bark- and wood-boring insects in the decline of Scots pine (Pinus sylvestris) in the Swiss Rhone valley |
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| Q114081937 | Assumed effects of invasive intraguild predators and how to avoid the snowball effect of unsupported expectations |
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| Q125352981 | Asymmetric impacts of two herbivore ecotypes on similar host plants |
| Q56543749 | Asymmetric priority effects influence the success of invasive forest insects |
| Q57229285 | Asymmetrical competition and amensalism through soil dumping by the ant, Myrmicaria natalensis |
| Q60564068 | Asymmetrical thermal constraints on the parapatric species boundaries of two widespread generalist butterflies |
| Q60537670 | Asynchronous temporal variation among sites in condition of two carabid species |
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| Q115531903 | Avian predation on the palatable butterfly, Cercyonis pegala (Satyridae) |
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| Q57638054 | Avoidance responses of an aphidophagous ladybird,Adalia bipunctata, to aphid-tending ants |
| Q125873374 | Back to Africa: autumn migration of the painted lady butterfly Vanessa cardui is timed to coincide with an increase in resource availability |
| Q57016356 | Bacterial symbionts as mediators of ecologically important traits of insect hosts |
| Q60537439 | Ballooning propensity of canopy and understorey spiders in a mature temperate hardwood forest |
| Q57554770 | Barley exposed to aerial allelopathy from thistles (Cirsium spp.) becomes less acceptable to aphids |
| Q125357984 | Bees provide pollination service to Campsis radicans (Bignoniaceae), a primarily ornithophilous trumpet flowering vine |
| Q126183664 | Beetles, parasitoids and tropical morning glories: a study in host discrimination |
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| Q56083359 | Behaviour of late-instar gypsy moth larvae in high and low density populations |
| Q56996864 | Behaviour of male and female parasitoids in the field: influence of patch size, host density, and habitat complexity |
| Q125879708 | Behaviour of specialist and generalist caterpillars on plantain (Plantago lanceolata) |
| Q115531860 | Behavioural activity levels and expression of stress proteins under predation risk in two damselfly species |
| Q60546081 | Behavioural and chemical mechanisms of plant-mediated deterrence and attraction among frugivorous insects |
| Q125853875 | Behavioural changes in Schistocerca gregaria following infection with a fungal pathogen: implications for susceptibility to predation |
| Q113798955 | Behavioural ecology of defence in a risky environment: caterpillarsversusants in a Neotropical savanna |
| Q126201363 | Behavioural flexibility does not prevent numerical declines of harvester ants under intense livestock grazing |
| Q125877571 | Behavioural modification of a social spider by a parasitoid wasp |
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| Q57201233 | Being a generalist herbivore in a diverse world: how do diets from different grasslands influence food plant selection and fitness of the grasshopperChorthippus parallelus? |
| Q113798954 | Below-ground nematode herbivory of resistant soybean cultivars impairs the performances of an above-ground caterpillar and its parasitoid |
| Q60523868 | Belowground infections of the invasivePhytophthora plurivorapathogen enhance the suitability of red oak leaves to the generalist herbivoreLymantria dispar |
| Q56378124 | Beneath the bark: associations among Sirex noctilio development, bluestain fungi, and pine host species in North America |
| Q115532864 | Benefit of actively mixing prey in a plant‐inhabiting predatory mite |
| Q113033931 | Bergmann's rule in larval ant lions: testing the starvation resistance hypothesis |
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| Q114146081 | Between locality variations in the seasonal patterns of dung beetles: the role of phenology in mitigating global warming effects |
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| Q57154535 | Biodiversity of stream insects in the Malaysian Peninsula: spatial patterns and environmental constraints |
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| Q113798274 | Biosystematics of the Muellerianella complex (Homoptera, Delphacidae): host-plants, habitats and phenology |
| Q125877796 | Biotic filtering and mass effects in small shrub patches: is arthropod community structure predictable based on the quality of the vegetation? |
| Q114081934 | Blacklegged tick population synchrony between oak forest and non‐oak forest |
| Q125826476 | Bloodmeal‐stealing in wild‐caught Mepraia spinolai (Hemiptera: Reduviidae), a sylvatic vector of Trypanosoma cruzi |
| Q126203256 | Body size and social dominance influence breeding dispersal in malePachydiplax longipennis(Odonata) |
| Q113206429 | Body size as an estimator of production costs in a solitary bee |
| Q57061791 | Body size changes in ground beetle assemblages ? a reanalysis of Braun et al. (2004)'s data |
| Q114930010 | Body size determines the outcome of competition for webs among alien and native sheetweb spiders (Araneae: Linyphiidae) |
| Q57057673 | Body size distribution in aphids: relative surface area of specific plant structures |
| Q129080870 | Body size explains interspecific variation in size–latitude relationships in geographically widespread beetle species |
| Q114080769 | Body size variation among invertebrates inhabiting different canopy microhabitat: flower visitors are smaller |
| Q59415058 | Both female castes contribute to colony emigration in the polygynous antMystrium oberthueri |
| Q61951058 | Bottom-up and top-down effects in a tritrophic system: the population dynamics of Plutella xylostella (L.)-Cotesia plutellae (Kurdjumov) on different host plants |
| Q57057293 | Bottom-up effects of glucosinolate variation on aphid colony dynamics in wild cabbage populations |
| Q113033983 | Bottom‐up and top‐down forces in plant‐gall relationships: testing the hypotheses of resource concentration, associational resistance, and host fitness reduction |
| Q124838582 | Bottom‐up, top‐down, and within‐trophic level pressures on a cactus‐feeding insect |
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| Q60506454 | Brochosome influence on parasitisation efficiency of Homalodisca coagulata (Say) (Hemiptera: Cicadellidae) egg masses by Gonatocerus ashmeadi Girault (Hymenoptera: Mymaridae) |
| Q111264017 | Bromeliads provide shelter against fire to mutualistic spiders in a fire-prone landscape |
| Q60484942 | Brood ball size but not egg size correlates with maternal size in a dung beetle,Onthophagus atripennis |
| Q56268449 | Brood raiding and the population dynamics of founding and incipient colonies of the fire ant, Solenopsis invicta |
| Q56460490 | Bumble bee pollen use and preference across spatial scales in human-altered landscapes |
| Q60466352 | Bumble bee species exhibit divergent responses to urbanisation in a Southern California landscape |
| Q57613575 | Bumble bee workers drift to conspecific nests at field scales |
| Q56431716 | Bumble bees selectively use native and exotic species to maintain nutritional intake across highly variable and invaded local floral resource pools |
| Q57045344 | Butterflies show flower colour preferences but not constancy in foraging at four plant species |
| Q111829907 | Butterfly habitats, broad-scale biotope affiliations, and structural exploitation of vegetation at finer scales: the matrix revisited |
| Q57607693 | COMMENT - The size-grain hypothesis in ants: conflicting evidence or confounded perspective? |
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| Q57057607 | Can the assumption of a non-random search improve our prediction of butterfly fluxes between resource patches? |
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| Q56566424 | Cannibalism and the stage-dependent transmission of a viral pathogen of the Indian meal moth, Plodia interpunctella |
| Q113855222 | Canopy herbivore community structure: large-scale geographical variation and relation to forest composition |
| Q57887793 | Carbohydrate scarcity increases foraging activities and aggressiveness in the antProlasius advenus(Hymenoptera: Formicidae) |
| Q57030710 | Carnivores and carotenoids are associated with adaptive behavioural divergence in a radiation of gall midges |
| Q115532930 | Cascading effects of cannibalism in a top predator |
| Q57247137 | Cascading effects of variation in plant vigour on the relative performance of insect herbivores and their parasitoids |
| Q112800852 | Cascading extinctions as a hidden driver of insect decline |
| Q112810949 | Caste-specific N and C isotope ratios in fungus-growing termites with special reference to uric acid preservation and their nutritional interpretation |
| Q115532938 | Caterpillars escape predation in habitat and thermal refuges |
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| Q126062333 | Causes of vertical stratification in the density of Cameraria hamadryadella |
| Q56442057 | Changes in egg colour, egg weight and oviposition rate with the number of eggs laid by wild females of the small heath butterfly, Coenonympha pamphilus |
| Q115555395 | Changes in feeding behaviour of the larvae of the damselfly Enallagma cyathigerum in response to stimuli from predators |
| Q126125321 | Changes in needle quality and larch bud moth performance in response to CO2 enrichment and defoliation of treeline larches |
| Q125404615 | Changes in pollinators' flower visits and activities potentially drive a diurnal turnover of plant‐pollinator interactions |
| Q56210098 | Chinese mantids gut toxic monarch caterpillars: avoidance of prey defence? |
| Q59270637 | Choice of flowers by foraging honey bees (Apis mellifera): possible morphological cues |
| Q58934804 | Choosy mothers pick challenging plants: maternal preference and larval performance of a specialist herbivore are not linked |
| Q57122156 | Clarifying misunderstandings regarding vegetation self-organisation and spatial patterns of fairy circles in Namibia: a response to recent termite hypotheses |
| Q106114959 | Climate change‐driven body size shrinking in a social wasp |
| Q112810954 | Climate warming experiments: are tents a potential barrier to interpretation? |
| Q125604317 | Clumped distribution patterns in goldenrod aphids: genetic and ecological mechanisms |
| Q115432264 | Clutch size in frugivorous insects as a function of host firmness: the case of the tephritid fly Anastrepha ludens |
| Q113798246 | Coastal insect herbivore communities are affected more by local environmental conditions than by plant genotype |
| Q113798249 | Coastal insect herbivore populations are strongly influenced by environmental variation |
| Q111172575 | Coexistence between two fruit fly species is supported by the different strength of intra- and interspecific competition |
| Q125974358 | Coexistence of two species of Binella Motchulsky (Coleoptera: Ptiliidae) and the significance of their adaptation to different temperature ranges |
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| Q55870937 | Colonising aliens: caterpillars (Lepidoptera) feeding on Piper aduncum and P. umbellatum in rainforests of Papua New Guinea |
| Q114626883 | Colonization, survival, and causes of mortality of Camerariu hamadryadella (Lepidoptera: Gracillariidae) on four species of host plants |
| Q113033935 | Colony ergonomics for a desert-dwelling bumblebee species (Hymenoptera: Apidae) |
| Q113271260 | Colony founding in the primitively eusocial wasp, Ropalidia marginata (Hymenoptera: Vespidae) |
| Q55870935 | Colony productivity and foundress behaviour of a native wasp versus an invasive social wasp |
| Q113272070 | Colony‐level chemical profiles do not provide reliable information about colony size in the honey bee |
| Q115532939 | Colour change ability and its effect on prey capture success in femaleMisumenoides formosipescrab spiders |
| Q57201253 | Colour morph related performance in the meadow grasshopperChorthippus parallelus(Orthoptera, Acrididae) |
| Q125779863 | Colour‐coded sampling: the pan trap colour preferences of oligolectic and nonoligolectic bees associated with a vernal pool plant |
| Q115405450 | Come to the dark side! The role of functional traits in shaping dark diversity patterns of south‐eastern European hoverflies |
| Q125658223 | Come to the dark side: habitat selection of larval odonates depends on background visual patterns |
| Q60546323 | Community structure and abundance of insects in response to early-season aphid infestation in wild cabbage populations |
| Q111376444 | Community structure of arboreal caterpillars within and among four tree species of the eastern deciduous forest |
| Q60568383 | Community-wide impact of an exotic aphid on introduced tall goldenrod |
| Q60568361 | Community-wide impacts of early season herbivory on flower visitors on tall goldenrod |
| Q113798953 | Community-wide responses to predation risk: effects of predator hunting mode on herbivores, pollinators, and parasitoids |
| Q115405463 | Comparative evidence supports a role for reproductive allocation in the evolution of female ornament diversity |
| Q125936852 | Comparative life‐history traits in a fig wasp community: implications for community structure |
| Q54582693 | Comparative nutritional ecology of bryophyte and angiosperm feeders in a sub-Antarctic weevil species complex (Coleoptera: Curculionidae) |
| Q115405455 | Comparative responses of termite functional and taxonomic diversity to land‐use change |
| Q57032000 | Comparing and contrasting life history variation in four aphid hyperparasitoids |
| Q113798944 | Comparing the plant–herbivore network topology of different insect guilds in Neotropical savannas |
| Q37727533 | Comparison of the wing polyphenic response of pea aphids (Acyrthosiphon pisum) to crowding and predator cues |
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| Q58649260 | Competition as a factor underlying the abundance of an uncommon phytophagous insect, the salt-marsh planthopper Delphacodes penedetecta |
| Q111172576 | Competition between the native and the introduced hornetsVespa crabroandVespa velutina: a comparison of potentially relevant life-history traits |
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| Q58729752 | Elevational trends in butterfly phenology: implications for species responses to climate change |
| Q115532921 | Elevationally biased avian predation as a contributor to the spatial distribution of geometrid moth outbreaks in sub-arctic mountain birch forest |
| Q123209423 | Emergence of flies from overwintering populations of cabbage root fly pupae |
| Q115405527 | Emergent effects of ground beetles size diversity on the strength of prey suppression |
| Q99962857 | Encapsulation of parasitoid eggs in soft scales (Homoptera: Coccidae)* |
| Q115531867 | Endophytic fungi decrease available resources for the aphid Rhopalosiphum padi and impair their ability to induce defences against predators |
| Q125920439 | Endosymbionts mediate the effects of antibiotic exposure in the tramp ant Cardiocondyla obscurior |
| Q57052512 | Energy reserves of parasitoids depend on honeydew from non-hosts |
| Q56785103 | Entomogenous fungi in tropical forest ecosystems: an appraisal |
| Q57201204 | Entomopathogenic fungi stimulate transgenerational wing induction in pea aphids, Acyrthosiphon pisum (Hemiptera: Aphididae) |
| Q57205129 | Environmental and geographical determinants of beta diversity of leaf beetles (Coleoptera: Chrysomelidae) in the Iberian Peninsula |
| Q125687834 | Environmental conditions and their impact on immunocompetence and pathogen susceptibility of the Caribbean termite Nasutitermes acajutlae |
| Q112798579 | Environmental context alters ecological trade-offs controlling ant coexistence in a spatially heterogeneous region |
| Q115405475 | Environmental diversity constrains learning inDrosophila melanogaster |
| Q59221308 | Environmental features influencing Carabid beetle (Coleoptera) assemblages along a recently deglaciated area in the Alpine region |
| Q57196933 | Escape from natural enemies during climate-driven range expansion: a case study |
| Q112800858 | Essential but invisible: non‐apparent but widespread ant nests favour soil nutrients and plant growth in semi‐arid areas |
| Q60267102 | Estimating changes in mean population age using the death distributions of live-captured medflies |
| Q115432296 | Estimating global biodiversity: tropical beetles and wasps send different signals |
| Q113271256 | Estimating the population size of specialised solitary bees |
| Q125847375 | Estimating the susceptibility of tree species to attack by the gypsy moth, Lymantria dispar |
| Q57016364 | Estimation of dispersal distances of the obligately plant-associated ant Crematogaster decamera |
| Q54571196 | Euphorine phylogeny: the evolution of diversity in host-utilization by parasitoid wasps (Hymenoptera: Braconidae) |
| Q63000336 | Evaluating a putative mimetic relationship between two butterflies, Adelpha bredowii and Limenitis lorquini |
| Q57777984 | Evaluating female remating rates in light of spermatophore degradation in Heliconius butterflies: pupal-mating monandry versus adult-mating polyandry |
| Q112800853 | Evaluating intraspecific variation in insect trait analysis |
| Q115532942 | Evergreen foliage allows early hatching in a pine processionary moth and escape from predation |
| Q110744799 | Evidence for a substantial host-use bottleneck following the invasion of an exotic, polyphagous weevil |
| Q29304690 | Evidence for hilltopping in bumblebees? |
| Q110809108 | Evidence for mate-encounter Allee effect in an invasive longhorn beetle (Coleoptera: Cerambycidae) |
| Q111263886 | Evidence for mutualism between a flower-piercing carpenter bee and ocotillo: use of pollen and nectar by nesting bees |
| Q111172573 | Evidence for the transfer of a soil-borne contaminant from plants to ants via an aphid mediator |
| Q113174562 | Evolution of host acceptance and its reversibility in a seed beetle |
| Q56773248 | Evolution of increased cold tolerance during range expansion of the elongate hemlock scaleFiorinia externaFerris (Hemiptera: Diaspididae) |
| Q112207609 | Evolutionary conservatism of geographic variation in host preference in Callosobruchus maculatus |
| Q60287784 | Expansion of the winter moth outbreak range: no restrictive effects of competition with the resident autumnal moth |
| Q115555383 | Experimental evidence for predation risk sensitive oviposition by a mosquito, Culiseta longiareolata |
| Q124983772 | Experimental evidence for weak effects of fire ants in a naturally invaded pine‐savanna ecosystem in north Florida |
| Q111264007 | Experimental field test of the influence of generalist stingless bees (Meliponini) on the topology of a bee–flower mutualistic network in the tropics |
| Q57411588 | Experimental logging alters the abundance and community composition of ovipositing mosquitoes in the southern Appalachians |
| Q62545864 | Experimental suppression of ants foraging on rainforest vegetation in New Guinea: testing methods for a whole-forest manipulation of insect communities |
| Q126045596 | Experimental warming disrupts reproduction and dung burial by a ball‐rolling dung beetle |
| Q115532219 | Exposure of arthropod predators to Cry1Ab toxin in Bt maize fields |
| Q126986112 | Exposure to potentially cannibalistic conspecifics induces an increased immune response |
| Q122204295 | Exposure to the neonicotinoid imidacloprid disrupts sex allocation cue use during superparasitism in the parasitoid waspNasonia vitripennis |
| Q57066782 | Extended larval development time for aphid parasitoids in the presence of plant endosymbionts |
| Q107316476 | Extreme ecological stoichiometry of a bark beetle–fungus mutualism |
| Q113389133 | Facial area and hairiness of pollinators visiting semi‐natural grassland wild plants predict their facial pollen load |
| Q113798941 | Facilitation between invasive herbivores: hemlock woolly adelgid increases gypsy moth preference for and performance on eastern hemlock |
| Q57532377 | Facultative bacterial endosymbionts benefit pea aphids Acyrthosiphon pisum under heat stress |
| Q111344621 | Facultative defences and specialist herbivores? Cinnabar moth (Tyria jacobaeae) on the re growth foliage of ragwort (Senecio jacobaea) |
| Q60270912 | Faithful vertical transmission but ineffective horizontal transmission of bacterial endosymbionts during sexual reproduction of the black bean aphid,Aphis fabae |
| Q56926827 | Feeding ecology and phylogenetic structure of a complex neotropical termite assemblage, revealed by nitrogen stable isotope ratios |
| Q60233918 | Feeding strategies in drosophilid parasitoids: the impact of natural food resources on energy reserves in females |
| Q124826549 | Feeny revisited: condensed tannins as anti‐herbivore defences in leaf‐chewing herbivore communities of Quercus |
| Q113173196 | Female-biased sex ratio in a wild bruchid seed-predator, Kytorhinus sharpianus. I. Larval competition and other factors |
| Q112810952 | Females of the European beewolf preserve their honeybee prey against competing fungi |
| Q112800877 | Field experiments show contradictory short‐ and long‐term myrmecochorous plant impacts on seed‐dispersing ants |
| Q60578811 | Field studies on flooding and survival of overwintering large heath butterfly Coenonympha tullia larvae on Fenn’s and Whixall Mosses in Shropshire and Wrexham, U.K |
| Q57637966 | Fighting in fig wasps: do males avoid killing brothers or do they never meet them? |
| Q114081922 | Fire affects galling insect communities through vegetation changes in a subtropical seasonally semiarid forest |
| Q55839589 | Fire ant predation on native and introduced subterranean termites in the laboratory: effect of high soldier number in Coptotermes formosanus |
| Q56936813 | Fire ants are drivers of biodiversity loss: a reply to King and Tschinkel (2013) |
| Q115405530 | Fire ants are not drivers of biodiversity change: a response to Stuble et al. (2013) |
| Q57069035 | Fire effects on insect herbivores in an oak savanna: the role of light and nutrients |
| Q60540008 | Fire? They don't give a dung! The resilience of dung beetles to fire in a tropical savanna |
| Q59085444 | First record of an apparently rare fig wasp feeding strategy: obligate seed predation |
| Q112798589 | Fit for succession - community structure and life strategies of leafhoppers in urban brownfields |
| Q59700254 | Fitness advantage from nuptial gifts in female fireflies |
| Q122966059 | Fitness and microbial networks of the common wasp, Vespula vulgaris (Hymenoptera: Vespidae), in its native and introduced ranges |
| Q111263875 | Fitness consequences of nest infiltration by the mutualist-exploiterMegalomyrmex adamsae |
| Q60449904 | Fitness costs and benefits of shelter building and leaf trenching behaviour in a pyralid caterpillar |
| Q62589144 | Fitness of two sibling species of Asobara (Braconidae:Alysiinae), larval parasitoids of Drosophilidae in different microhabitats |
| Q125119817 | Flexibility in the composition and concentration of amino acids in honeydew of the drepanosiphid aphidTuberculatus quercicola |
| Q60506524 | Flexible larval development and the timing of destructive feeding by a solitary endoparasitoid: an optimal foraging problem in evolutionary perspective |
| Q115555365 | Flexible use of patch marks in an insect predator: effect of sex, hunger state, and patch quality |
| Q58430234 | Flight activity of adult stoneflies in relation to weather |
| Q120068805 | Flight morphology corresponds to both surrounding landscape structure and local patch conditions in a highly specialized peatland butterfly (Lycaena epixanthe) |
| Q113272066 | Floral bagging differentially affects handling behaviours and single‐visit pollen deposition by honey bees and native bees |
| Q113272052 | Floral resource continuity boosts bumble bee colony performance relative to variable floral resources |
| Q59845931 | Floral resource pulse decreases bumble bee foraging trip duration in central Wisconsin agroecosystem |
| Q113272078 | Floral resources, body size, and surrounding landscape influence bee community assemblages in oak-savannah fragments |
| Q112798588 | Floral visitation patterns of two invasive ant species and their effects on other hymenopteran visitors |
| Q112798577 | Floral visitors and ant scent marks: noticed but not used? |
| Q117787901 | Florivory is an alternative but suboptimal diet for an invasive leaf‐feeding beetle |
| Q57065163 | Flower-heads, herbivores, and their parasitoids: food web structure along a fertility gradient |
| Q55869711 | Flowers at the front line of invasion? |
| Q114367504 | Fluctuating asymmetry in relation to two fitness components, adult longevity and male mating success in a ladybird beetle, Harmonia axyridis (Coleoptera: Coccinellidae) |
| Q125860211 | Fluctuations in the abundance of butterflies, 1976–82 |
| Q112798584 | Foliage-age mixing within balsam fir increases the fitness of a generalist caterpillar |
| Q67311511 | Foliar damage, parasitoids and indirect competition: a test using herbivores of birch |
| Q57032102 | Food plant and herbivore host species affect the outcome of intrinsic competition among parasitoid larvae |
| Q125314655 | Food resource partition in the beech leaf‐feeding guild |
| Q59117612 | Forage collection, substrate preparation, and diet composition in fungus-growing ants |
| Q56873711 | Foraging activity and dietary spectrum of wood ants (Formica rufagroup) and their role in nutrient fluxes in boreal forests |
| Q57242911 | Foraging activity of leaf-cutting ants changes light availability and plant assemblage in Atlantic forest |
| Q61883747 | Foraging and courtship behaviour in males of the solitary bee Anthophora plumipes (Hymenoptera: Anthophoridae): thermal physiology and the roles of body size |
| Q115532223 | Foraging behaviour influences the outcome of predator-predator interactions |
| Q115555381 | Foraging behaviour of caterpillars given a choice of plant genotypes in the presence of insect predators |
| Q58803201 | Foraging by honeybees on Carduus acanthoides: pattern and efficiency |
| Q125584841 | Foraging by the carabid Agonum dorsale in the field |
| Q125564568 | Foraging byAtta sexdens(Formicidae: Attini): seasonal patterns, caste and efficiency |
| Q125574846 | Foraging ecology and patterns of diversification in dipteran parasitoids of fire ants in south Brazil |
| Q59270703 | Foraging ecology of hoverflies: morphology of the mouthparts in relation to feeding on nectar and pollen in some common urban species |
| Q128900801 | Foraging preferences of ants on a heterogeneous Brazilian sandy shore habitat |
| Q57002157 | Foraging trip duration of bumblebees in relation to landscape-wide resource availability |
| Q117219566 | Forest and grassland habitats support pollinator diversity more than wildflowers and sunflower monoculture |
| Q126049847 | Forest complexity drives dung beetle assemblages along an edge‐interior gradient in the southwest Amazon rainforest |
| Q100252554 | Forests do not limit bumble bee foraging movements in a montane meadow complex |
| Q60504207 | Frequency-dependent and density-dependent larval competition between life-history strains of a fly, Lucilia cuprina |
| Q115405402 | Friend and foe? The effects of grassland management on global patterns of spider diversity |
| Q36370288 | Friend or foe: inter-specific interactions and conflicts of interest within the family. |
| Q126628621 | From dusk till dawn: camera traps reveal the diel patterns of flower feeding by hawkmoths |
| Q112800840 | From forest to forestry: Reassembly of spider communities after native forest replacement by pine monocultures |
| Q111419163 | From logs to landscapes: determining the scale of ecological processes affecting the incidence of a saproxylic beetle |
| Q127713104 | Fruit‐breeding drosophilids (Diptera) in the Neotropics: playing the field and specialising in generalism? |
| Q114627164 | Functional benefits of predator species diversity depend on prey identity |
| Q57013944 | Functional diversity decreases with temperature in high elevation ant fauna |
| Q112664016 | Functional resin use in solitary bees |
| Q112800839 | Functional responses to anthropogenic disturbance and the importance of selected traits: A study case using dung beetles |
| Q115432300 | GENETIC STRUCTURE AND LOCAL ADAPTATION IN NATURAL INSECT POPULATIONS. Edited by Susan Mopper and Sharon Y. Strauss. Chapman and Hall, New York. 1998. Hardback, £65.00. ISBN 0-412-08031-1. |
| Q59987721 | Gall wasps and their parasitoids in cork oak fragmented forests |
| Q115405504 | Gall-forming insects in a lowland tropical rainforest: low species diversity in an extremely specialised guild |
| Q106206106 | Gallers as leaf rollers: ecosystem engineering in a tropical system and its effects on arthropod biodiversity |
| Q54586288 | Generalist dung attraction response in a New Zealand dung beetle that evolved with an absence of mammalian herbivores |
| Q115531756 | Generalist predation on forest tent caterpillar varies with forest stand composition: an experimental study across multiple life stages |
| Q57265300 | Genetic and social structure of the queen size dimorphic ant Leptothorax cf. andrei |
| Q113173188 | Genetic divergence and ecological specialisation of seed weevils (Exapion spp.) on gorses (Ulex spp.) |
| Q115432261 | Genetic diversity and widespread haplotypes in a migratory dragonfly, the common green darnerAnax junius |
| Q56967819 | Genetic diversity, host-specificity and unusual phylogeography of a cryptic, host-associated species complex of gall-inducing scale insects |
| Q128162706 | Genetic mixing facilitates adaptation to a novel environmental constraint |
| Q30052095 | Genetic signature of the colonisation dynamics along a coastal expansion front in the damselflyCoenagrion scitulum |
| Q56961585 | Genetic, morphological, and dietary changes associated with novel habitat colonisation in the Canary Island endemic grasshopperAcrostira bellamyi |
| Q112798593 | Genotype and environment interact to influence acceptability and suitability of white spruce for a specialist herbivore, Zeiraphera canadensis |
| Q60466091 | Geographic differences in flash intervals and pre-mating isolation between populations of the Genji firefly, Luciola cruciata |
| Q113798940 | Geographic variation in performance of a widespread generalist insect herbivore |
| Q115531862 | Geographic variation in prey preference in bark beetle predators |
| Q59498299 | Geographic variation in reproductive success of the parasitoid Asobara tabida in larvae of several Drosophila species |
| Q57236251 | Geographical patterns of hoverfly (Diptera, Syrphidae) functional groups in Europe: inconsistency in environmental correlates and latitudinal trends |
| Q112798595 | Geographical variability in, and temperature effects on, the phenology of Maniola jurtina and Pyronia tithonus (Lepidoptera, Satyrinae) in England and Wales |
| Q56020366 | Geographical variation in food web structure in Nepenthes pitcher plants |
| Q59117924 | Geographical variation in host-ant specificity of the parasitic butterfly Maculinea alcon in Denmark |
| Q115532923 | Geographical variation in mandible morphologies specialised for collembolan predation depend on prey size in the antStrumigenys lewisi |
| Q60430044 | Grain aphid clones vary in frost resistance, but this trait is not influenced by facultative endosymbionts |
| Q60573755 | Granivory in terrestrial isopods |
| Q60544922 | Grasshopper egg mortality mediated by oviposition tactics and fire intensity |
| Q114081910 | Gregarious caterpillars shorten their larval development time in response to simulated predation threat |
| Q57008059 | Growth, development, and life-history strategies in an unpredictable environment: case study of a rare hoverflyBlera fallax(Diptera, Syrphidae) |
| Q57230058 | Guards and thieves: antagonistic interactions between two ant species coexisting on the same ant-plant |
| Q112810951 | Gut content analysis and a new feeding group classification of termites |
| Q119652630 | Gut content metabarcoding of three widespread Iberian ant‐eating spiders reveals specialisation on the same abundant harvester ants |
| Q56419303 | Habitat association and coexistence of endemic and introduced ant species in the Galápagos Islands |
| Q115555347 | Habitat edges as a potential ecological trap for an insect predator |
| Q110789466 | Habitat loss and degradation due to farming intensification modify the floral visitor assemblages of a semiarid keystone shrub |
| Q125867890 | Habitat selection in a large orb‐weaving spider: vegetational complexity determines site selection and distribution |
| Q111264019 | Habitat variation, mutualism and predation shape the spatio-temporal dynamics of tansy aphids |
| Q114081948 | Hanging in the treetops: anin situexperiment in ancient hemlock assessing outbreak defoliator performance among crown levels |
| Q113173183 | Harvester ants modify seed rain using nest vegetation and granivory |
| Q114645827 | Health food versus fast food: the effects of prey quality and mobility on prey selection by a generalist predator and indirect interactions among prey species |
| Q125477074 | Heatwaves increase larval mortality and delay development of a solitary bee |
| Q56998913 | Herbivore-induced plant responses inBrassica oleraceaprevail over effects of constitutive resistance and result in enhanced herbivore attack |
| Q113798959 | Herbivorous insect decreases plant nutrient uptake: the role of soil nutrient availability and association of below-ground symbionts |
| Q113798248 | Herbivorous insect species in the tree canopy of a relict South African forest |
| Q56783318 | Herbivory alters resource allocation and compensation in the invasive tree Melaleuca quinquenervia |
| Q125777840 | Herbivory by subterranean termite colonies and the development of fairy circles in SW Namibia |
| Q114146070 | Hiding among holes: mechanisms underlying the evolution of masquerade in flea beetles (Chrysomelidae) |
| Q125630667 | High densities of leaf‐tiers in open habitats are explained by host plant architecture |
| Q115396868 | High local species richness of parasitic wasps (Hymenoptera: Ichneumonidae; Pimplinae and Rhyssinae) from the lowland rainforests of Peruvian Amazonia |
| Q113798929 | High temperature and soil moisture reduce host‐plant quality for an insect herbivore |
| Q56837350 | Higher gregarine parasitism often in sibling species of host damselflies with smaller geographical distributions |
| Q60254796 | Higher investment in flight morphology does not trade off with fecundity estimates in a poleward range-expanding damselfly |
| Q56619633 | Higher productivity at the cost of increased host-specificity when Maculinea butterfly larvae exploit ant colonies through trophallaxis rather than by predation |
| Q60535368 | Historical dynamics of a native cerambycid, Enaphalodes rufulus, in relation to climate in the Ozark and Ouachita Mountains of Arkansas |
| Q113272053 | Homing ability in a tropical Asian stingless bee is influenced by interaction between release distances and urbanisation |
| Q127183318 | Honeydew composition and its effect on life‐history parameters of hyperparasitoids |
| Q57638075 | Horizontal transmission of Wolbachia in a Drosophila community |
| Q59271065 | Host choice byAphidius colemani: effects of plants, plant-aphid combinations and the presence of intra-guild predators |
| Q60271086 | Host genotype affects the relative success of competing lines of aphid parasitoids under superparasitism |
| Q59732134 | Host phylogeny and nutrient content drive galler diversity and abundance on willows |
| Q115396460 | Host plant associations, diversity and species—area relationships of mesophyll-feeding leafhoppers of trees and shrubs in Britain |
| Q57434232 | Host plant direct defence against eggs of its specialist herbivore, Heliothis subflexa |
| Q57031711 | Host plant effects on the behavioural phenotype of a Chrysomelid |
| Q58039825 | Host plant finding in the specialised leaf beetle Cassida canaliculata: an analysis of small-scale movement behaviour |
| Q57886949 | Host plant growth characteristics as determinants of abundance and phenology in jumping plant-lice on downy willow |
| Q129965620 | Host plant nitrogen enrichment has both positive and negative effects on the larval growth of a specialist butterfly |
| Q113181752 | Host plant phenology may determine the abundance of an ecosystem engineering herbivore in a tropical savanna |
| Q119583044 | Host plant selection by Cerambycidae in two different strata in association with seasonality and physical wood characteristics in a tropical dry forest |
| Q99966699 | Host plant specificity in several species of generalist mite predators |
| Q125015177 | Host plant taxonomy and phenotype influence the structure of a neotropical host plant-hispine beetle food web |
| Q60568405 | Host plant variation in plant-mediated indirect effects: moth boring-induced susceptibility of willows to a specialist leaf beetle |
| Q57251443 | Host plants and butterfly biology. Do host-plant strategies drive butterfly status? |
| Q57032080 | Host preference and offspring performance are linked in three congeneric hyperparasitoid species |
| Q112798590 | Host preferences in a phonotactic parasitoid of field crickets: the relative importance of host song characters |
| Q117787911 | Host quality does not matter to native or invasive cactus moth larvae: grave implications for North American prickly pears |
| Q112800843 | Host repertoires and changing insect–plant interactions |
| Q56771656 | Host selection and sex ratio in a heteronomous hyperparasitoid |
| Q57001784 | Host shifting by Operophtera brumata into novel environments leads to population differentiation in life-history traits |
| Q62545902 | Host specificity of ambrosia and bark beetles (Col., Curculionidae: Scolytinae and Platypodinae) in a New Guinea rainforest |
| Q60488020 | Host tree architecture mediates the effect of predators on herbivore survival |
| Q58261262 | Host utilisation by moth and larval survival of pine processionary caterpillar Thaumetopoea pityocampa in relation to food quality in three Pinus species |
| Q58875715 | Host-plant quality adaptively affects the diapause threshold: evidence from leaf beetles in willow plantations |
| Q112798587 | Host-plant quality alters grass/forb consumption by a mixed-feeding insect herbivore,Melanoplus bivittatus(Orthoptera: Acrididae) |
| Q60526335 | Host-plant use in the range expansion of the pine processionary moth, Thaumetopoea pityocampa |
| Q99974494 | Host-specificity constrains evolutionary host change in the psyllid Prosopidopsylla flava |
| Q125659678 | Host‐searching responses to herbivory‐associated chemical information and patch use depend on mating status of female solitary parasitoid wasps |
| Q128209541 | Host‐size decisions of female parasitoid wasps seeking hidden hosts |
| Q115213296 | How climate change affects the seasonal ecology of insect parasitoids |
| Q110626362 | How do invasive species affect native species? Experimental evidence from a carrion blowfly (Diptera: Calliphoridae) system |
| Q113173194 | How labile are the egg-laying preferences of seed beetles? |
| Q113033934 | How many species are there in apple insect communities?: testing the resource diversity and intermediate disturbance hypotheses |
| Q36533344 | How much flower-rich habitat is enough for wild pollinators? Answering a key policy question with incomplete knowledge |
| Q34308399 | Hunger-dependent and Sex-specific Antipredator Behaviour of Larvae of a Size-dimorphic Mosquito |
| Q113855240 | INDUCED RESPONSES TO HERBIVORY. |
| Q115405386 | Identification of the missing links in parasite–host networks using the dark diversity concept: a case study with two taxonomic groups of ectoparasitic arthropods and small mammalian hosts |
| Q115532960 | Identifying inter- and intra-guild feeding activity of an arthropod predator assemblage |
| Q60394670 | Identity and combinations of arbuscular mycorrhizal fungal isolates influence plant resistance and insect preference |
| Q62569357 | Immediate protein dietary effects on movement and the generalised immunocompetence of migrating Mormon cricketsAnabrus simplex(Orthoptera: Tettigoniidae) |
| Q59208719 | Impact of an invasive alien ant,Wasmannia auropunctataRoger., on a specialised plant-ant mutualism,Barteria fistulosaMast. andTetraponera aethiopsF. Smith., in a Gabon forest |
| Q115555352 | Impact of avian and arthropod predation on lepidopteran caterpillar densities and plant productivity in an ephemeral agroecosystem |
| Q113036795 | Impact of diet quality on demographic attributes in adult grasshoppers and the nitrogen limitation hypothesis |
| Q36851532 | Impact of inter- and intra-specific competition among larvae on larval, adult, and life-table traits of Aedes aegypti and Aedes albopictus females |
| Q60329512 | Impact of intraguild predation on parasitoid foraging behaviour |
| Q125681030 | Impact of non‐pathogenic bacteria on insect disease resistance: importance of ecological context |
| Q58883932 | Impact of plant cover on the cavity-nesting ant Temnothorax crassispinus |
| Q112800872 | Impact of seed abundance on seed processing and dispersal by the red ant Myrmica rubra |
| Q56776519 | Impacts of Argentine ants on mealybugs and their natural enemies in California’s coastal vineyards |
| Q56439895 | Impacts of exotic spider spillover on resident arthropod communities in a natural habitat |
| Q123242031 | Impacts of grazing intensity and increased precipitation on a grasshopper assemblage (Orthoptera: Acrididae) in a meadow steppe |
| Q117043577 | In plateaus, land cover replaced climate as the vital environmental factor on the spatial composition of bumblebees with the altitude rising |
| Q56431696 | Indirect effects of grazing intensity on pollinators and floral visitation |
| Q111264022 | Indirect mutualism: ants protect fig seeds and pollen dispersers from parasites |
| Q115405445 | Individual tree context and contrast dictate tree physiological features and arthropod biodiversity patterns across multiple trophic levels |
| Q56332538 | Individually mark-mass release-resight study elucidates effects of patch characteristics and distance on host patch location by an insect herbivore |
| Q125564494 | Individual‐resource network between Xylocopa bees and plant resources: generalist species, specialist individuals? |
| Q113855233 | Induced Plant Defenses Against Pathogens And Herbivores: Biochemistry, Ecology And Agriculture. |
| Q56386067 | Industrial and non-industrial melanism in the peppered moth,Bistort betularia(L.) |
| Q56779402 | Infestation of commercial bumblebee (Bombus impatiens) field colonies by small hive beetles (Aethina tumida) |
| Q111264023 | Infiltration of a facultative ant-plant mutualism by the introduced Argentine ant: effects on mutualist diversity and mutualism benefits |
| Q56987536 | Influence of adult nutrition on the relationship between body size and reproductive parameters in a parasitoid wasp |
| Q113855226 | Influence of atmospheric carbon dioxide enrichment on induced response and growth compensation after herbivore damage inLotus corniculatus |
| Q29013488 | Influence of egg size differences within egg clutches on larval parameters in nine libellulid species (Odonata) |
| Q57039045 | Influence of extrafloral nectary phenology on ant-plant mutualistic networks in a neotropical savanna |
| Q125387070 | Influence of feeding guild on insect response to host plant fertilization |
| Q125407009 | Influence of generalist stingless bees on the structure of mutualistic flower–pollinator networks in the tropics: Temporal variation |
| Q112798592 | Influence of habitat structure on the phonotactic strategy of a parasitoid flyEmblemasoma auditrix |
| Q125589920 | Influence of host plant heterogeneity on the distribution of a birch aphid |
| Q113798250 | Influence of inter-tree variation in time of budburst of white spruce on herbivory and the behaviour and survivorship of Zeiraphera canadensis |
| Q113798252 | Influence of intra-tree variation in time of budburst of white spruce on herbivory and the behaviour and survivorship of Zeiraphera canadensis |
| Q57200008 | Influence of leaf traits on the spatial distribution of arboreal arthropods within an overstorey rainforest tree |
| Q110099054 | Influence of male mating history on female reproductive success among monandrous Naryciinae (Lepidoptera: Psychidae) |
| Q56996912 | Influence of presence and spatial arrangement of belowground insects on host-plant selection of aboveground insects: a field study |
| Q124925846 | Influence of the predatory backswimmer, Notonecta maculata, on invertebrate community structure |
| Q57008296 | Influence of urbanisation on the prevalence of protozoan parasites of bumblebees |
| Q67311513 | Influences of host feeding-niche and foodplant type on generalist and specialist parasitoids |
| Q60573904 | Influences of two life-history stages of the weevil,Larinus minutus, on its host plantCentaurea diffusa |
| Q115405479 | Insect biodiversity meets ecosystem function: differential effects of habitat and insects on carrion decomposition |
| Q113033936 | Insect chemosensory responses: a chemical legacy hypothesis |
| Q125875090 | Insect colonisation sequences in bracts of Heliconia caribaea in Puerto Rico |
| Q113033986 | Insect diversity over 36 years at a protected Sierra Nevada (California) site: towards an evaluation of the insect apocalypse hypothesis |
| Q113798273 | Insect herbivore guilds and species—area relationships: leafminers on British trees |
| Q111263883 | Insect herbivore stoichiometry: the relative importance of host plants and ant mutualists |
| Q125919890 | Insect immune priming: ecology and experimental evidences |
| Q120064088 | Insect invasion sequences: systematic or stochastic? |
| Q113272067 | Insect pollinators show constancy for different flower traits between the most‐ and less‐preferred plants: a case study of the long‐proboscid tangle‐veined fly |
| Q114081929 | Insect predation reduces the abundance of a nidicolous ectoparasite |
| Q112800854 | Insect responses to global change offer signposts for biodiversity and conservation |
| Q114081906 | Insect‐plant‐fungus interactions in mycorrhizal associations, with a focus on spittlebugs and ectomycorrhizal host plants |
| Q56999038 | Instar-specific sensitivity of specialist Manduca sexta larvae to induced defences in their host plant Nicotiana attenuata |
| Q57032084 | Integrating more biological and ecological realism into studies of multitrophic interactions |
| Q60362660 | Inter-individual variation in movement: is there a mobility syndrome in the large white butterfly Pieris brassicae? |
| Q60362607 | Inter-individual variation in shivering behaviour in the migratory painted lady Vanessa cardui |
| Q62925313 | Inter-sexual combat and resource allocation into body parts in the spider, Stegodyphus lineatus |
| Q126203605 | Interaction of specialist root and shoot herbivores of Alliaria petiolata and their impact on plant performance and reproduction |
| Q112800867 | Interactions among body size, trophic level, and dispersal traits predict beetle detectability and occurrence responses to fire |
| Q126007099 | Interactions between Apion species (Coleoptera: Curculionidae) and Polygonaceae. I. Apion curtirostre Germ, and Rumex acetosa L. |
| Q115532225 | Interactions between a hunting spider and a web-builder: consequences of intraguild predation and cannibalism for prey suppression |
| Q106377791 | Interactions between cottonwood and beavers positively affect sawfly abundance |
| Q60233785 | Interactions between granivorous and omnivorous ants in a desert grassland: results from a long-term experiment |
| Q56781654 | Interactions between introduced and native predatory ladybirds (Coleoptera, Coccinellidae): factors influencing the success of species introductions |
| Q55871054 | Interactions with native mosquito larvae regulate the production of Aedes albopictus from bromeliads in Florida |
| Q113855244 | Interactive effects of herbivory and sand burial on growth of a tropical dune plant, Ipomoea pes-caprae |
| Q57715589 | Interdemic variation of cannibalism in a wolf spider (Pardosa monticola) inhabiting different habitat types |
| Q115532959 | Interference competition, not predation, explains the negative association between wood ants (Formica rufa) and abundance of ground beetles (Coleoptera: Carabidae) |
| Q111172591 | Interguild interactions between a non‐native phloem feeder and a native outbreaking defoliator |
| Q113173204 | Interspecific competition between insect herbivores: asymmetric competition between cinnabar moth and the ragwort seed-head fly |
| Q115153020 | Interspecific host discrimination and competition in Apoanagyrus (Epidinocarsis) lopezi and A.(E.)diversicornis, parasitoids of the cassava mealybug Phenacoccus manihoti |
| Q112800868 | Interspecific plant functional variation prevails over intraspecific variation in driving spider beta diversity |
| Q126073894 | Inter‐ and intra‐sexual variation in immune defence in the cabbage white butterfly, Pieris rapae L. (Lepidoptera: Pieridae) |
| Q110737026 | Intra- and interspecific variation in trophic ecology of ‘predatory’ ants in the subfamily Ponerinae |
| Q56765647 | Intra-floral resource partitioning between endemic and invasive flower visitors: consequences for pollinator effectiveness |
| Q115531868 | Intra-guild predation and variation in egg defence between sympatric and allopatric populations of two species of ladybird beetles |
| Q113855224 | Intra-guild predation relaxes natural enemy impacts on herbivore populations |
| Q111952320 | Intra-specific body size variation in Polistes paper wasps as a response to social parasite pressure |
| Q56768725 | Intra-specific host preference forLittoraria filosaby the dipteran parasitoidSarcophaga megafilosia: the consequences of attacking individuals outside the preferred size range |
| Q56774947 | Intraguild predation of the aphid pathogenic fungus Pandora neoaphidis by the invasive coccinellid Harmonia axyridis |
| Q111172574 | Intraspecific aggression and the colony structure of the invasive ant Myrmica rubra |
| Q104206113 | Intraspecific aggression, colony identity and foraging distances in Sudanese Microtermes spp. (Isoptera: Termitidae: Macrotermitinae) |
| Q114367508 | Intraspecific competition amongst larval Aedes aegypti: food exploitation or chemical interference? |
| Q113798277 | Intraspecific variability in herbivore performance and host quality: a field study of Uroleucon caligatum (Homoptera: Aphididae) and its Solidago hosts (Asteraceae) |
| Q60163561 | Intraspecific variability in host plant quality and ovipositionaI preferences in Eucheira socialis (Lepidoptera: Pieridae) |
| Q111425945 | Intraspecific variation in beech scale populations and in susceptibility of their host Fagus sylvatica |
| Q112800859 | Intraspecific variation in host plant traits mediates taxonomic and functional composition of local insect herbivore communities |
| Q33708760 | Intrinsic and extrinsic drivers of succession: Effects of habitat age and season on an aquatic insect community |
| Q57032145 | Intrinsic competition among solitary and gregarious endoparasitoid wasps and the phenomenon of ‘resource sharing’ |
| Q57032035 | Intrinsic competition between primary hyperparasitoids of the solitary endoparasitoidCotesia rubecula |
| Q56559533 | Invading and resident defoliators in a changing climate: cold tolerance and predictions concerning extreme winter cold as a range-limiting factor |
| Q117044794 | Invasion of the coccinellid community associated with a tropical annual agroecosystem |
| Q59270453 | Invasive ants-are fire ants drivers of biodiversity loss? |
| Q114081921 | Invasive intraguild predators: Evidence of their effects, not assumptions |
| Q111172597 | Invasive paper wasps have strong cascading effects on the host plant of monarch butterflies |
| Q117787927 | Invasive plant population and herbivore identity affect latex induction |
| Q115531899 | Invertebrate predation of leaf-miners at low densities |
| Q113174514 | Is elevation a strong environmental filter? Combining taxonomy, functional traits and phylogeny of butterflies in a tropical mountain |
| Q60511777 | Is it enemy-free space? The evidence for terrestrial insects and freshwater arthropods |
| Q59504692 | Is natural selection a plausible explanation for the distribution of Idh-1 alleles in the cricket Allonemobius socius? |
| Q60569118 | Is optimal foraging a realistic expectation in orb-web spiders? |
| Q54637600 | Is the matrix a sea? Habitat specificity in a naturally fragmented landscape |
| Q115405494 | Is there any evidence that aphid alarm pheromones work as prey and host finding kairomones for natural enemies? |
| Q126013162 | Isotope evidence for latitudinal migrations of the dragonfly Sympetrum fonscolombii (Odonata: Libellulidae) in Middle Asia |
| Q115405378 | Ivermectin impacts on dung beetle diversity and their ecological functions in two distinct Brazilian ecosystems |
| Q113855228 | Jasmonate-mediated induced plant resistance affects a community of herbivores |
| Q54646984 | Kleptoparasitic behaviour of Aphodius rufipes (L.) larvae in nests of Geotrupes spiniger Marsh. (Coleoptera, Scarabaeidae) |
| Q115405459 | Knitting patterns of biodiversity, range size and body size in aquatic beetle faunas: significant relationships but slightly divergent drivers |
| Q115531881 | Laboratory study of cannibalism and interspecific predation in ladybirds |
| Q61755388 | Lack of evidence for reproductive isolation among ecologically specialised lycaenid butterflies |
| Q115532887 | Lack of prey switching and strong preference for mosquito prey by a temporary pond specialist predator |
| Q57002290 | Landscape context affects trap-nesting bees, wasps, and their natural enemies |
| Q59401658 | Large-scale migration synchrony between parasitoids and their host |
| Q115532953 | Larger clutches of chemically defended butterflies reduce egg mortality: evidence fromBattus philenor |
| Q115396306 | Larger wildflower plantings increase natural enemy density, diversity, and biological control of sentinel prey, without increasing herbivore density |
| Q125743895 | Largest on earth: Discovery of a new type of fairy circle in Angola supports a termite origin |
| Q112798596 | Larval aestivation and direct development as alternative strategies in the speckled wood butterfly, Pararge aegeria, in Sweden |
| Q115555370 | Larval defence against ant predation in the butterfly Smyrna blomfildia |
| Q115396319 | Larval experience induces adult aversion to rearing host plants: a novel behaviour contrary to Hopkins' host selection principle |
| Q116524571 | Larval food affects oviposition preference, female fecundity and offspring survival in Yponomeuta evonymellus |
| Q57031734 | Larval food composition affects courtship song and sperm expenditure in a lekking moth |
| Q67311515 | Latitudinal body-size gradients for the bees of the eastern United States |
| Q115396443 | Latitudinal effects on treehopper species richness (Hornoptera: Membracidae) |
| Q115396432 | Latitudinal gradients in ichneumonid species-richness in Australia |
| Q60449900 | Latitudinal variation in the phenological responses of eastern tent caterpillars and their egg parasitoids |
| Q115531793 | Leaf domatia reduce intraguild predation among predatory mites |
| Q113798254 | Leaf miners on Ochna ciliata (Ochnaceae) growing on Aldabra Atoll: patterns of herbivory in relation to goat browsing and exposure to the sun |
| Q57032442 | Leaf mining in the Myrtaceae |
| Q112490754 | Leaf phenology mediates provenance differences in herbivore populations on valley oaks in a common garden |
| Q113173200 | Leaf shape and the host-finding behaviour of two ovipositing monophagous butterfly species |
| Q37266013 | Leaf species identity and combination affect performance and oviposition choice of two container mosquito species |
| Q60504251 | Leaf tissue transport as a function of loading ratio in the leaf-cutting ant Atta cephalotes |
| Q62006979 | Leaf traits of congeneric host plants explain differences in performance of a specialist herbivore |
| Q57242931 | Leaf-cutting ants as ecosystem engineers: topsoil and litter perturbations aroundAtta cephalotesnests reduce nutrient availability |
| Q128022230 | Let's mate here and now – seasonal constraints increase mating efficiency |
| Q60518037 | Lethal and sublethal behavioural responses of saline water beetles to acute heat and osmotic stress |
| Q59599601 | Life cycle and food availability indices in Notiophilus biguttatus (Coleoptera, Carabidae) |
| Q59151716 | Life history consequences of larval foraging depth differ between two competing Anopheles mosquitoes |
| Q56267954 | Life history of Kladothrips ellobus and Oncothrips rodwayi: insight into the origin and loss of soldiers in gall-inducing thrips |
| Q113173195 | Life history traits related to resource partitioning between synhospitalic species of Colocasiomyia (Diptera, Drosophilidae) breeding in inflorescences of Alocasia odora (Araceae) |
| Q112800886 | Life in harsh environments: carabid and spider trait types and functional diversity on a debris-covered glacier and along its foreland |
| Q115555359 | Life-history responses of a mayfly to seasonal constraints and predation risk |
| Q115034295 | Life-history trait variation in a queen-size dimorphic ant |
| Q63975887 | Life-history, genotypic, and environmental correlates of clutch size in the Glanville fritillary butterfly |
| Q112798591 | Limitation of nesting resources for ants in Colombian forests and coffee plantations |
| Q117705401 | Limited direct effects of a massive wildfire on its sagebrush steppe bee community |
| Q60519715 | Limited effects of dominant ants on assemblage species richness in three Amazon forests |
| Q60271120 | Limited scope for maternal effects in aphid defence against parasitoids |
| Q54653878 | Limiting the potential for intraspecific competition: regulation of Trioza eugeniae oviposition on unexpanded leaf tissue |
| Q57064703 | Linking the bacterial community in pea aphids with host-plant use and natural enemy resistance |
| Q115532856 | Living in an urban pod: Seed predation and parasitism of bruchid beetles in a native tree species |
| Q60135428 | Load size selection by foraging leaf-cutter ants (Atta cephalotes) |
| Q114145171 | Local adaptations of life-history traits of a Drosophila parasitoid, Leptopilina boulardi: does climate drive evolution? |
| Q128709488 | Local and regional climate variables driving spring phenology of tortricid pests: a 36 year study |
| Q114081945 | Local climate mediates spatial and temporal variation in carabid beetle communities in three forests in Mount Odaesan, Korea |
| Q60546995 | Local dynamics of worker activity of the invasiveVespula germanicaandV. vulgaris(Hymenoptera: Vespidae) wasps in Argentina |
| Q67236719 | Local grassland restoration affects insect communities |
| Q56938617 | Local host ant specificity of Phengaris (Maculinea) teleius butterfly, an obligatory social parasite of Myrmica ants |
| Q62545937 | Local versus regional species richness in tropical insects: one lowland site compared with the island of New Guinea |
| Q57008028 | Location of bumblebee nests is predicted by counts of nest-searching queens |
| Q115532920 | Locking out predators by silk, a new counterattack behaviour in a social spider mite |
| Q113798243 | Long- and short-term changes in plant growth following simulated herbivory: adaptive responses to damage? |
| Q56333772 | Long-distance dispersal of non-native pine bark beetles from host resources |
| Q59387715 | Long-term after-effects of cold exposure in adult Alphitobius diaperinus (Tenebrionidae): the need to link survival ability with subsequent reproductive success |
| Q57049669 | Long-term changes in ground beetle (Coleoptera: Carabidae) assemblages in Scotland |
| Q59345473 | Long-term dynamics of leaf miners, Eriocrania spp., on mountain birch: alternate year fluctuations and interaction with Epirrita autumnata |
| Q56780396 | Long-term impact of exotic ants on the native ants of Madeira |
| Q114146069 | Longer daylengths associated with poleward range shifts accelerate aphid extinction by parasitoid wasps |
| Q60405559 | Lower thermal tolerance in nocturnal than in diurnal ants: a challenge for nocturnal ectotherms facing global warming |
| Q109040606 | Low‐temperature tolerance in coprophagic beetle species (Coleoptera: Scarabaeidae): implications for ecological services |
| Q115396398 | Lycaenid butterflies and plants: is myrmecophily associated with amplified hostplant diversity? |
| Q56444604 | Maintenance of body-size variation and host range in the orange-tip butterfly: evidence for a trade-off between adult life-history traits |
| Q112800892 | Male disguised females: costs and benefits of female-limited dimorphism in a butterfly |
| Q122204312 | Male field crickets that provide reproductive benefits to females incur higher costs |
| Q111593545 | Male golden egg bugs ( Phyllomorpha laciniata Vill.) do not preferentially accept their true genetic offspring; comment on the paper by García-González et al. (2005, Ecological Entomology , 30, 444-455) |
| Q121851466 | Male mate choice based on chemical cues in the cricketAcheta domesticus(Orthoptera: Gryllidae) |
| Q64947268 | Male pheromone composition depends on larval but not adult diet in Heliconius melpomene. |
| Q99955061 | Male size and survival: the effects of male combat and bird predation in Dawson's burrowing bees, Amegilla dawsoni |
| Q57247132 | Male-biased size dimorphism in ichneumonine wasps (Hymenoptera: Ichneumonidae) - the role of sexual selection for large male size |
| Q125791811 | Male‐biased sex ratios in mature damselfly populations: real or artefact? |
| Q112800855 | Management actions shape dung beetle community structure and functional traits in restored tallgrass prairie |
| Q55841820 | Marginal range expansion in a host-limited butterfly species Gonepteryx rhamni |
| Q122748299 | Market basket analysis of grasshopper (Orthoptera: Acrididae) assemblages in eastern Wyoming: a 17-year case study using associative analysis for ecological insights into grasshopper outbreaks |
| Q114081923 | Massive spider web aggregations in South American grasslands after flooding |
| Q56699864 | Mate finding, dispersal, number released, and the success of biological control introductions |
| Q57486828 | Mate preference for novel partners in the cricket Gryllus bimaculatus |
| Q115532904 | Maternal effects across life stages: larvae experiencing predation risk increase offspring provisioning |
| Q57251325 | Measuring dispersal and detecting departures from a random walk model in a grasshopper hybrid zone |
| Q113798260 | Measuring herbivory |
| Q128346896 | Mechanisms driving component Allee effects during invasions: using a biological control agent as model invader |
| Q115531886 | Mechanisms of predator accumulation in a mixed crop system |
| Q57201177 | Mechanisms of species-sorting: effect of habitat occupancy on aphids' host plant selection |
| Q127851977 | Mechanisms structuring host–parasitoid networks in a global warming context: a review |
| Q56168431 | Mesophyll cell-sucking herbivores (Cicadellidae: Typhlocybinae) on rainforest trees in Papua New Guinea: local and regional diversity of a taxonomically unexplored guild |
| Q110762747 | Metacommunity patterns of highly diverse stream midges: gradients, chequerboards, and nestedness, or is there only randomness? |
| Q110762566 | Metacommunity structure analysis reveals nested patterns in deconstructed macroinvertebrates assemblages |
| Q56690009 | Micro-climate determines oviposition site selection and abundance in the butterflyPyrgus armoricanusat its northern range margin |
| Q112800857 | Microbes make the meal: oligolectic bees require microbes within their host pollen to thrive |
| Q114146065 | Microbial volatiles and succession of beetles on small carrion |
| Q114081927 | Microclimatic edge effects in a fragmented forest: disentangling the drivers of ecological processes in plant‐leafminer‐parasitoid food webs |
| Q104206114 | Microclimatic factors associated with elevational changes in army ant density in tropical montane forest |
| Q99962878 | Microhabitat specialization and similarity of scale-insect assemblages on different fruit trees and in different countries |
| Q57251328 | Migration and Allee effects in the six-spot burnet moth Zygaena filipendulae |
| Q60379852 | Mimicry in the burnet moth Zygaena ephialtes: population studies and evidence of a Batesian—Müllerian situation |
| Q59112176 | Mismatch between the timing of oviposition and the seasonal optimum. The stochastic phenology of Mediterranean acorn weevils |
| Q60235037 | Mixed effects of habitat fragmentation on species richness and community structure in a microarthropod microecosystem |
| Q113798267 | Mixed function oxidases and herbivore polyphagy: the devil's advocate position |
| Q113855239 | Mixture models of soybean growth and herbivore performance in response to nitrogen-sulphur-phosphorous nutrient interactions |
| Q112798580 | Mobility is related to species traits in noctuid moths |
| Q59653754 | Moisture content and nutrition as selection forces for emerald ash borer larval feeding behaviour |
| Q107968340 | Monarch butterflies reared under autumn‐like conditions have more efficient flight and lower post‐flight metabolism |
| Q60562772 | More food, less habitat: how necromass and leaf litter decomposition combine to regulate a litter ant community |
| Q56210059 | More than just fish food: ecosystem services provided by freshwater insects |
| Q112800841 | More than meets the eye: decrypting diversity reveals hidden interaction specificity between frogs and frog‐biting midges |
| Q59270496 | Morphological correlates of nectar production used by honeybees |
| Q111264005 | Morphological matching and phenological overlap promote niche partitioning and shape a mutualistic plant–hawkmoth network |
| Q115532958 | Mothers vigilantly guard nests after partial brood loss: a cue of nest predation risk in a paper wasp |
| Q113798925 | Movement of nest‐searching bumblebee queens reflects nesting habitat quality |
| Q56690063 | Movement of the Apollo butterfly Parnassius apollo related to host plant and nectar plant patches |
| Q56772451 | Movement, colonization, and establishment success of a planthopper of prairie potholes,Delphacodes scolochloa(Hemiptera: Delphacidae) |
| Q59426851 | Moving beyond the guild concept: developing a practical functional trait framework for terrestrial beetles |
| Q56805474 | Mud puddling by butterflies is not a simple matter |
| Q113174538 | Multitrophic interactions drive body size variations in seed‐feeding insects |
| Q128614665 | Multi‐scale oviposition site selection in two mosquito species |
| Q112800850 | Multi‐species occupancy models: an effective and flexible framework for studies of insect communities |
| Q107316473 | Mutualism is not restricted to tree‐killing bark beetles and fungi: the ecological stoichiometry of secondary bark beetles, fungi, and a scavenger |
| Q113174512 | Myrmecochorous plants and their ant seed dispersers through successional stages in temperate cove forests |
| Q115532941 | Natural enemies of natural enemies: the potential top-down impact of predators on entomopathogenic nematode populations |
| Q125865631 | Natural enemy impacts on Bemisia tabaci (MEAM1) dominate plant quality effects in the cotton system |
| Q60505581 | Natural history of whitefly in Costa Rica: an evolutionary starting point |
| Q125582589 | Natural pupation sites of swallowtail butterflies (Lepidoptera: Papilioninae): Papilio polyxenes Fabr., P.glaucus L. and Battus philenor (L.) |
| Q126171939 | Nectar usage in a southern Arizona hawkmoth community |
| Q115405433 | Negative effects of urbanisation on the physical condition of an endemic dung beetle from a neotropical hotspot |
| Q115531863 | Negative interactions between chemical resistance and predators affect fitness in soybeans |
| Q111289102 | Negative spatial covariation in abundance of two European ticks: diverging niche preferences or biotic interaction? |
| Q113855248 | Neighbourhood affects a plant's risk of herbivory and subsequent success |
| Q60317156 | Neither the devil nor the deep blue sea: larval mortality factors fail to explain the abundance and distribution of Tischeria ekebladella |
| Q122653068 | Neonicotinoids override a parasite exposure impact on hibernation success of a key bumblebee pollinator |
| Q115396464 | Nerium oleander as an alternative host plant for south Florida milkweed bugs, Oncopeltus fasciatus |
| Q99966957 | Nest construction and larval behaviour of Bubas bison (L.) and Bubas bubalus (01.) (Coleoptera, Scarabaeidae) |
| Q61307542 | Nest site choice by the intertidal spider Desis formidabilis (Araneae: Desidae) and nest utilisation by its hymenopteran egg parasitoid |
| Q112800851 | Nesting habitat of ground‐nesting bees: a review |
| Q55878852 | Nettle-feeding nymphalid butterflies: temperature, development and distribution |
| Q113271254 | Networks and dominance hierarchies: does interspecific aggression explain flower partitioning among stingless bees? |
| Q113174528 | Neutral and niche‐based factors simultaneously drive seed and invertebrate removal by red harvester ants |
| Q113282464 | Niche differentiation in nectar-collecting stingless bees: the influence of morphology, floral choice and interference competition |
| Q112810958 | Nitrogen and carbon isotope ratios in termites: an indicator of trophic habit along the gradient from wood‐feeding to soil‐feeding |
| Q59117572 | No benefit in diversity? The effect of genetic variation on survival and disease resistance in a polygynous social insect |
| Q60287726 | No regulatory role for adult predation in cyclic population dynamics of the autumnal moth,Epirrita autumnata |
| Q120170076 | No water, no eggs: insights from a warming outdoor mesocosm experiment |
| Q56939927 | Nocturnal resource defence in aphid-tending ants of northern Patagonia |
| Q55952513 | Non-morph specific predation of peppered moths (Biston betularia) by bats |
| Q59565406 | Non-random distribution among a guild of parasitoids: implications for community structure and host survival |
| Q113798918 | Non‐native stinging ant interactions with native anurans |
| Q124973118 | Non‐trophic effects of oribatid mites on cord‐forming basidiomycetes in soil microcosms |
| Q111376486 | Not all matrix habitat is created equal for rare bee species in forest habitat |
| Q113798935 | Novel evidence for systemic induction of silicon defences in cucumber following attack by a global insect herbivore |
| Q59117659 | Novel fungal disease in complex leaf-cutting ant societies |
| Q113174511 | Numbers matter: Predatory ability increases with forager group size in omnivorous ant species with similar predatory traits |
| Q57048859 | Nutrients, diversity, and community structure of two phytotelm systems in a lower montane forest, Puerto Rico |
| Q115555380 | Nutritional benefits of intraguild predation and cannibalism among generalist and specialist phytoseiid mites |
| Q113036792 | Nutritional benefits of the leaf-mining behaviour of two grass miners: a test of the selective feeding hypothesis |
| Q56050306 | Nutritional condition influences investment by male katydids in nuptial food gifts |
| Q60023584 | Nutritional versus genetic correlates of caste differentiation in a desert ant |
| Q57275405 | Observations of the flight behaviour of the army worm moth, Spodoptera exempta, at an emergence site using radar and infra-red optical techniques |
| Q125882399 | Observations on the biology of Subcoccinella vigintiquattuor‐punctata (L.) in southern England |
| Q60537463 | Occurrence patterns of aspen-feeding wood-borers (Coleoptera: Cerambycidae) along the wood decay gradient: active selection for specific host types or neutral mechanisms? |
| Q125580526 | Odonates, gregarines and water mites: why are the same host species infected by both parasites? |
| Q112798586 | On the analysis of non-linear allometries |
| Q59270386 | On the role of sinigrin (mustard oil) in a tritrophic context: plant-aphid-aphidophagous hoverfly |
| Q115555394 | Ontogenetic change of prey preference in the generalist predator Zelus renardii and its influence on predator-predator interactions |
| Q60537474 | Ontogenetic shifts in competitive interactions and intra-guild predation between two wolf spider species |
| Q114627623 | Ontogenic colour change, survival, and mating in the damselflyAgriocnemis pygmaeaRambur (Insecta: Odonata) |
| Q35648342 | Ontogeny of worker body size distribution in bumble bee (Bombus impatiens) colonies |
| Q115531872 | Opportunistic predation and offspring sex ratios of cicada-killer wasps (Sphecius speciosus Drury) |
| Q113033990 | Optimal progeny body size in a solitary bee,Osmia bicornis(Apoidea: Megachilidae) |
| Q115532934 | Optimal range of prey size for antlions |
| Q57057676 | Optimum body size in aphids |
| Q67311510 | Organization of a parasitoid community associated with a complex of galls on Atriplex spp. in southern California |
| Q60164433 | Organization of predator assemblages in Neotropical tree holes: effects of abiotic factors and priority |
| Q57436753 | Origin of termite eusociality: trophallaxis integrates the social, nutritional, and microbial environments |
| Q57724745 | Original Article |
| Q57340186 | Overdispersion of Allothrombium pulvinum larvae (Acari: Trombidiidae) parasitic on Aphis gossypii (Homoptera: Aphididae) in cotton fields |
| Q113798262 | Overwintering survivorship of pupae of the mimosa web worm, Homadaula anisocentra (Lepidoptera: Plutellidae), in an urban landscape |
| Q113798258 | Oviposition by herbivorous insects on spider webs as an anti-predation defence |
| Q37657654 | Oviposition habitat selection by container-dwelling mosquitoes: responses to cues of larval and detritus abundances in the field |
| Q56771451 | Oviposition habitat selection for a predator refuge and food source in a mosquito |
| Q60487993 | Oviposition patterns and larval damage by the invasive horse-chestnut leaf minerCameraria ohridellaon different species ofAesculus |
| Q115555364 | Oviposition patterns in a predatory mite reduce the risk of egg predation caused by prey |
| Q43047632 | Oviposition preference and offspring performance in container breeding mosquitoes: evaluating the effects of organic compounds and laboratory colonisation |
| Q115396323 | Oviposition preference of Lycaena salustiusfor, and larval performance on, a novel host plant: an example of ecological fitting |
| Q57005604 | Oviposition preference of a Eucalyptus herbivore and the importance of leaf age on interspecific host choice |
| Q59270552 | Oviposition preferences of aphidophagous hoverflies |
| Q58042227 | Oviposition substrate affects adult mortality, independent of reproduction, in the seed beetle Callosobruchus maculatus |
| Q114627624 | Oviposition, larval survival and leaf damage by the willow leaf blotch miner,Micrurapteryx salicifoliella,in relation to leaf trichomes across 10Salixspecies |
| Q112800895 | Parabiotic ants: the costs and benefits of symbiosis |
| Q60504166 | Parallel foraging cycles for different resources in leaf-cutting ants: a clue to the mechanisms of rhythmic activity |
| Q56931665 | Parallel host range expansion in two unrelated cossid moths infestingEucalyptus nitenson two continents |
| Q113174516 | Parallel host‐plant‐associated differences in an extended phenotype between populations of six species of gall‐forming insects |
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| Q115531877 | Parasitism and predation as agents of mortality of winter moth populations in neglected apple orchards in Nova Scotia |
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| Q125660734 | Parasitoids affect plant responses through their host Pieris brassicae, but not for the benefit of their own performance |
| Q57742170 | Parasitoids use herbivore-induced information to adapt patch exploitation behaviour |
| Q59024493 | Parental care influences social immunity in burying beetle larvae |
| Q56837342 | Parthenogenesis did not consistently evolve in insular populations ofIschnura hastata(Odonata, Coenagrionidae) |
| Q57198930 | Past attacks influence host selection by the solitary bark beetleDendroctonus micans |
| Q60525715 | Patch choice from a distance and use of habitat information during foraging by the parasitoid Ibalia leucospoides |
| Q126099469 | Patch exploitation strategies of parasitoids under indirect intra‐ and inter‐specific competition |
| Q57208150 | Patch size effects are more important than genetic diversity for plant-herbivore interactions in Brassica crops |
| Q114367778 | Paternal effects associated with melanism inHarmonia axyridis(Coleoptera: Coccinellidae): mating sequence asymmetries and interactions with age-specific maternal effects |
| Q58924902 | Paternity analysis in the golden egg bug using AFLPs: do the males preferentially accept their true genetic offspring? |
| Q122453783 | Paternity and female remating in Requena verticalis (Orthoptera: Tettigoniidae) |
| Q59024323 | Pathogen and immune dynamics during maturation are explained by Bateman's Principle |
| Q57220159 | Patterns in the abundance and distribution of ichneumonid parasitoids within and across habitat patches |
| Q59159087 | Patterns inVarroa destructordepend on bee host abundance, availability of natural resources, and climate in Mediterranean apiaries |
| Q125820647 | Patterns of abundance of fire ants and native ants in a native ecosystem |
| Q111493056 | Patterns of abundance, distribution, and alary polymorphism among the salt marsh Delphacidae (Homoptera: Fulgoroidea) of Northwest Florida |
| Q113798275 | Patterns of herbivory on Passiflora leaf tissues and species by generalized and specialized feeding insects |
| Q57452350 | Patterns of parasite infection in bumble bees (Bombusspp.) of Northern Virginia |
| Q56689173 | Patterns of pollen feeding and habitat preference among Heliconius species |
| Q115396863 | Patterns of species richness for blackflies (Diptera: Simuliidae) in the Nearctic and Neotropical regions |
| Q57607604 | Pay it forward: refuse dump from leaf-cutting ants promotes caterpillar digestive performance by increasing plant nitrogen content |
| Q115432309 | Payoffs of the two alternative nesting tactics in the African dung beetle, Scarabaeus catenatus |
| Q125910283 | Pea aphids (Acyrthosiphon pisum Harris) reduce secretion of extrafloral nectar in broad bean (Vicia faba) |
| Q60287869 | Performance of a spring-feeding moth in relation to time of oviposition and bud-burst phenology of different host species |
| Q57532367 | Persistence and regression of hearing in the exclusively diurnal moths, Trichodezia albovittata (Geometridae) and Lycomorpha pholus (Arctiidae) |
| Q64032558 | Persistence of experience effects in the parasitoid Trichogramma nr. brassicae |
| Q113033933 | Persistent size variation in the anthophorine bee Centris pallida (Apidae) despite a large male mating advantage |
| Q115555396 | Persistent, localized outbreaks in the western tussock moth Orgyia vetusta: the roles of resource quality, predation and poor dispersal |
| Q113173191 | Petal herbivory by chrysomelid beetles (Phyllotreta sp.) is detrimental to pollination and seed production in Lepidium papilliferum (Brassicaceae) |
| Q125405865 | Phenological imbalance in the supply and demand of floral resources: Half the pollen and nectar produced by the main autumn food source, Hedera helix, is uncollected by insects |
| Q57038926 | Phenological phases of the host plant shape plant-treehopper interaction networks |
| Q111425946 | Phenology and intensity of phyllophage attack on Fagus sylvatica in Wytham Woods, Oxford |
| Q54604148 | Phenology and life history of Belgica antarctica, an Antarctic midge (Diptera: Chironomidae) |
| Q58868948 | Phenology determines seasonal variation in ectoparasite loads in a natural insect population |
| Q115396370 | Phenotypic changes and reduced genetic diversity have accompanied the rapid decline of the garden tiger moth (Arctia caja) in the U.K. |
| Q113798280 | Phenotypic induction inPieris napiL.: role of temperature and photoperiod in a coastal California population |
| Q110615816 | Phenotypic plasticity and geographical variation in the pre-reproductive period of Autographa gamma (Lepidoptera: Noctuidae) and its implications for migration in this species |
| Q110615936 | Phenotypic plasticity in host-plant specialisation in Aphis fabae |
| Q110614786 | Phenotypic plasticity in hoverflies: the relationship between colour pattern and season in Episyrphus balteatus and other Syrphidae |
| Q110615821 | Phenotypic plasticity of thermal tolerance contributes to the invasion potential of Mediterranean fruit flies (Ceratitis capitata) |
| Q110615819 | Phenotypic plasticity ofBrevicoryne brassicaein responses to nutritional quality of two related host plants |
| Q110615815 | Phenotypic plasticity, seasonal climate and the population biology of Bicyclus butterflies (Satyridae) in Malawi |
| Q113173211 | Phenotypic variability in nesting success among Osmia lignaria propinqua females in a glasshouse environment: (Hymenoptera: Megachilidae) |
| Q110615818 | Phenotypic variation in colour pattern and seasonal plasticity in Eristalis hoverflies (Diptera: Syrphidae) |
| Q113173190 | Phenotypic variation in male and worker encapsulation response in the bumblebee Bombus terrestris |
| Q115396395 | Philopatry in the alpine grasshopper, Podisma pedestris: a novel experimental and analytical method |
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| Q108685652 | Photoperiod and variation in life history traits in core and peripheral populations in the damselflyLestes sponsa |
| Q60506313 | Phylloplane bacteria increase the negative impact of food limitation on insect fitness |
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| Q113798942 | Phytochemical defences and performance of specialist and generalist herbivores: a meta‐analysis |
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| Q115396336 | Plant patch structure modifies parasitoid assemblage richness of a specialist herbivore |
| Q113798919 | Plant silicon defences reduce the performance of a chewing insect herbivore which benefits a contemporaneous sap‐feeding insect |
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| Q57031691 | Plant species, mycorrhiza, and aphid age influence the performance and behaviour of a generalist |
| Q113798276 | Plant tannins and insect herbivores: an appraisal |
| Q115532943 | Plant traits mediate effects of predators across pepper (Capsicum annuum) varieties |
| Q60546333 | Plant-mediated effects of butterfly egg deposition on subsequent caterpillar and pupal development, across different species of wild Brassicaceae |
| Q60549592 | Plant-mediated effects of soil nitrogen enrichment on a chemically defended specialist herbivore, Calophasia lunula |
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| Q113272055 | Pollen analysis of cavity‐nesting bees (Hymenoptera: Anthophila) and their food webs in a city |
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| Q115396415 | Pondering the imponderable: a probability-based approach to estimating insect diversity from repeat faunal samples |
| Q58317477 | Population genetic structure of the winter moth, Operophtera brumata Linnaeus, in the Orkney Isles suggests long-distance dispersal |
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| Q115396378 | Potential novel hosts for the lily leaf beetle Lilioceris lilii Scopoli (Coleoptera: Chrysomelidae) in eastern North America |
| Q123024630 | Potential range expansion and niche shift of the invasive Hyphantria cunea between native and invasive countries |
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| Q111172594 | Predation and avoidance behaviour in aphid‐ladybird interactions of native and invasive ladybirds in Europe |
| Q115531879 | Predation and avoidance of tough leaves by aquatic larvae of the moth Parapoynx rugosalis (Lepidoptera: Pyralidae) |
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| Q56226330 | Predation by an exotic lizard,Anolis sagrei, alters the ant community structure in betelnut palm plantations in southern Taiwan |
| Q115531894 | Predation by wasps on lepidopteran larvae in an Ozark forest canopy |
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| Q115531898 | Predator gut state and prey detectability using electrophoretic analysis of gut contents |
| Q115532897 | Predator modulation of plant pathogen spread through induced changes in vector development rates |
| Q60482970 | Predator-induced spine length and exocuticle thickness inLeucorrhinia dubia(Insecta: Odonata): a simple physiological trade-off? |
| Q115531888 | Predator-mediated coexistence in laboratory communities of mycophagous Drosophila (Diptera: Drosophilidae) |
| Q114627631 | Predators marked with chemical cues from one prey have increased attack success on another prey species |
| Q115531856 | Predators mediate the effects of a fungal pathogen on prey: an experiment with grasshoppers, wolf spiders, and fungal pathogens |
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| Q113272054 | Proboscis curling in a pollinator causes extensive pollen movement and loss |
| Q110620584 | Propagule pressure rather than population growth determines colonisation ability: a case study using two phytophagous mite species differing in their invasive potential |
| Q56446112 | Proportion of exotics and relatedness of host species mediate the positive effect of plant richness on the species richness of fruit flies |
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| Q58875740 | Putting more eggs in the best basket: clutch-size regulation in the comma butterfly |
| Q60484809 | Putting your sons in the right place: the spatial distribution of fig wasp offspring inside figs |
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| Q57251258 | Quantifying the activity levels and behavioural responses of butterfly species to habitat boundaries |
| Q60264479 | Quantifying the benefits and costs of parental care in assassin bugs |
| Q124852514 | Quantifying the costs and benefits of protective egg coating in a Chrysomelid beetle |
| Q114146066 | Quantifying the post‐fire recovery of taxonomic and functional diversity of dung beetles in the Brazilian Pantanal |
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| Q112033119 | Rapid morphological change in stream beetle museum specimens correlates with climate change |
| Q113272065 | Rapid photogrammetry of morphological traits of free‐ranging moths |
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| Q113798939 | Realised toxicity of plant defences to an insect herbivore depends more on insect dehydration than on energy reserves |
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| Q112798594 | Regional diversity, local community structure and vacant niches: the herbivorous arthropods of bracken in South Africa |
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| Q112798585 | Relationship between body size and homing ability in the genusOsmia(Hymenoptera; Megachilidae) |
| Q56268464 | Relationship of queen number and queen relatedness in multiple-queen colonies of the fire ant Solenopsis invicta |
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| Q113173206 | Relationships between larval density, adult size and egg production in the cowpea seed beetle, Callosobruchus maculatus |
| Q60577395 | Relationships between oviposition date, hatch date, and offspring size in the grasshopper Chorthippus brunneus |
| Q115396385 | Relationships between the density and diversity of floral resources and flower visitor activity in a temperate grassland community |
| Q57077736 | Relative contributions of environmental and maternal factors to trans-generational immune priming inT. castaneum |
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| Q56547829 | Resource input and the community structure of larval infaunas of an eastern tropical pitcher plant Nepenthes bicalcarata |
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| Q56268430 | Response of fire ants (Formicidae: Solenopsis invicta and S.gerninata) to artificial nectars with amino acids |
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| Q125129890 | Role of ants in structuring the aphid community on apple |
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| Q115405437 | Role of saprophagous fly biodiversity in ecological processes and urban ecosystem services |
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| Q111172600 | Seasonal and landscape effects on the biotic resistance of forest communities to experimental insect introductions |
| Q113271365 | Seasonal change in offspring sex and size in Dawson's burrowing bees (Amegilla dawsoni) (Hymenoptera: Anthophorini) |
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| Q113036791 | Seasonal changes in leaf nutritional quality influence grass miner performance |
| Q114367495 | Seasonal cycles of assortative mating and reproductive behaviour in polymorphic populations ofHarmonia axyridisin China |
| Q56447432 | Seasonal decline in plant defence is associated with relaxed offensive oviposition behaviour in the viburnum leaf beetlePyrrhalta viburni |
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| Q110615817 | Seasonal phenotypic plasticity of wing melanisation in the cabbage white butterfly, Pieris rapae L. (Lepidoptera: Pieridae) |
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| Q61697991 | Seasonality and life cycles of woody plant-feeding noctuid moths (Lepidoptera: Noctuidae) in Mediterranean habitats |
| Q57232065 | Seasonality of spiders (Araneae) in Mediterranean ecosystems and its implications in the optimum sampling period |
| Q115405536 | Secondary galling: a novel feeding strategy among ‘non-pollinating’ fig wasps fromFicus curtipes |
| Q113710675 | Secondary seed dispersal by ants in Neotropical cerrado savanna: species-specific effects on seeds and seedlings ofSiparuna guianensis(Siparunaceae) |
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| Q56455930 | Seed handling behaviours of native and invasive seed-dispersing ants differentially influence seedling emergence in an introduced plant |
| Q113174560 | Seed manipulation by ants: disentangling the effects of ant behaviours on seed germination |
| Q63564606 | Seed predation by insects across a tropical forest precipitation gradient |
| Q113173186 | Seed weevils living on the edge: pressures and conflicts over body size in the endoparasiticCurculiolarvae |
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| Q59321265 | Selection for enemy-free space: eggs placed away from the host plant increase survival of a neotropical ithomiine butterfly |
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| Q111419161 | Semi-field experiments investigating facilitation: arrival order decides the interrelationship between two saproxylic beetle species |
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| Q125956482 | Setting the scene… meeting up with Darwin and Wallace |
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| Q128021675 | Sexual differences rather than flight performance underlie movement and exploration in a tropical butterfly |
| Q113173185 | Sexual selection did not contribute to the evolution of male lifespan under curtailed age at reproduction in a seed beetle |
| Q115034296 | Sexual size dimorphism and the integration of phenotypically plastic traits |
| Q56287888 | Sexually transmitted disease in a promiscuous insect, Adalia bipunctata |
| Q56985404 | Shaking a leg and hot to trot: the effects of body size and temperature on running speed in ants |
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| Q59321283 | Shift happens! Shifting balance and the evolution of diversity in warning colour and mimicry |
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| Q107968338 | Shifts in the community composition of caddisflies (Insecta: Trichoptera) in a subtropical river over three decades |
| Q115396369 | Short-term larval food stress and associated compensatory growth reduce adult immune function in a damselfly |
| Q112800842 | Short‐term positive effects of wildfire on diurnal insects and pollen transport in a Mediterranean ecosystem |
| Q126012235 | Show your true colour: cues for male mate preference in an intra‐specific mimicry system |
| Q129642496 | Shrub shading moderates the effects of weather on arthropod activity in arctic tundra |
| Q114081904 | Size and location of host‐plant shape the spatial pattern of forest insect |
| Q115532947 | Size and sex of cricket prey predict capture by a sphecid wasp |
| Q113271266 | Size-related foraging differences of bumble bee workers |
| Q112800871 | Size‐related life‐history traits in geometrid moths: a comparison of a temperate and a tropical community |
| Q113798263 | Skeletal economy in certain herbivorous beetles as an adaptation to a poor dietary supply of nitrogen |
| Q61883741 | Skewed sex ratios and multiple founding in galls of the oak apple gall wasp Biorhiza pallida |
| Q113036794 | Slow-growth, high-mortality - a general hypothesis, or is it? |
| Q62858154 | Small spermatophore size and reduced female fitness in an isolated butterfly population |
| Q56267951 | Social biology and sex ratios of the eusocial gall-inducing thrips Kladothrips hamiltoni |
| Q124877238 | Social but not solitary bee abundance tracks pollen protein accumulation in forest canopy gaps |
| Q59118117 | Social structure in the ant Lasius flavus: multi-queen nests or multi-nest mounds? |
| Q57039050 | Soil and vegetation features determine the nested pattern of ant-plant networks in a tropical rainforest |
| Q123264998 | Soil arthropod communities associated with Berberis thunbergii invasion in a temperate deciduous forest harbour more detritivores |
| Q113106835 | Soil surface complexity has a larger effect on food exploitation by ants than a change from grassland to shrubland |
| Q57249357 | Solar radiation directly affects larval performance of a forest insect |
| Q56987732 | Some aspects of the rate of increase of a coccinellid |
| Q112800847 | Some considerations on the terminology applied to dung beetle functional groups |
| Q125488273 | Sources of prey availability data alter interpretation of outputs from prey choice null networks |
| Q60128461 | Sources of variation in larval parasitism of two sympatrically outbreaking birch forest defoliators |
| Q115405461 | Spatial and temporal diversity in hyperparasitoid communities ofCotesia glomerataon garlic mustard,Alliaria petiolata |
| Q115396362 | Spatial and temporal dynamics of habitat selection across canopy gradients generates patterns of species richness and composition in aquatic beetles |
| Q113173494 | Spatial and temporal organisation of the pre-dispersal seed predator guild in a perennial legume, Vicia tenuifolia |
| Q56483742 | Spatial and temporal patterns of caterpillar performance and the suitability of two host plant species |
| Q115531890 | Spatial and temporal patterns of predation by ants on eggs of Cactoblastis cactorum |
| Q113173187 | Spatial and temporal variation in a suite of life-history traits in two species of wolf spider |
| Q57030810 | Spatial and temporal variation in the parasitoid assemblage of an exophytic polyphagous caterpillar |
| Q59849353 | Spatial correlations of Diceroprocta apache and its host plants: evidence for a negative impact from Tamarix invasion |
| Q112800885 | Spatial distribution, sampling efficiency and Taylor's power law |
| Q57196919 | Spatial ecology of multiple parasitoids of a patchily-distributed host: implications for species coexistence |
| Q112800861 | Spatial partitioning of perching on plants by tropical dung beetles depends on body size and leaf characteristics: a sit‐and‐wait strategy for food location |
| Q57008584 | Spatial patterns, temporal variability, and the role of multi-nest colonies in a monogynous Spanish desert ant |
| Q61951018 | Spatial variation in the magnitude and functional form of density-dependent processes on the large skipper butterflyOchlodes sylvanus |
| Q109780826 | Spatio‐temporal responses of butterflies to global warming on a Mediterranean island over two decades |
| Q115532905 | Specialisation in prey capture drives coexistence among sympatric spider‐hunting wasps |
| Q59271033 | Specialisation of bacterial endosymbionts that protect aphids from parasitoids |
| Q113174596 | Specialist pollinating seed predator exhibits oviposition strategy consistent with optimal oviposition theory |
| Q56047425 | Specializations and polyphagy of Plebejus argus (Lepidoptera: Lycaenidae) in North Wales |
| Q57638033 | Speciation in fig wasps |
| Q113174541 | Species associations and trait dissimilarity in communities of ectoparasitic arthropods harboured by small mammals at three hierarchical scales |
| Q57032577 | Species diversity and structure of phytophagous beetle assemblages along a latitudinal gradient: predicting the potential impacts of climate change |
| Q57200011 | Species number, species abundance and body length of arboreal arthropods associated with an Australian rainforest tree |
| Q115432267 | Species richness and parasitism in an assemblage of parasitoids attacking maize stem borers in coastal Kenya |
| Q115396377 | Species richness estimation and determinants of species detectability in butterfly monitoring programmes |
| Q115396874 | Species richness of phytophagous beetles in the tropical treeBrosimum utile(Moraceae): the effects of sampling strategy and the problem of tourists |
| Q113798938 | Species richness, range size, and wing development in South American melanopline grasshoppers (Orthoptera, Acrididae) |
| Q112810950 | Spiders and harvestmen as gastropod predators |
| Q115034290 | Spiders follow an ideal free distribution based on traits of the plant community |
| Q113855247 | Spore-feeding: a new, regionally vacant niche for bracken herbivores |
| Q34370681 | Stable Isotope Analysis Reveals Detrital Resource Base Sources of the Tree Hole Mosquito, Aedes triseriatus |
| Q112800856 | Stable isotope ecology in insects: a review |
| Q113033984 | Stingless bees (Apidae: Meliponini) seek sodium at carrion baits in Costa Rica |
| Q113174545 | Stronger dung removal in forests compared with grassland is driven by trait composition and biomass of dung beetles |
| Q113174549 | Structural changes over time in individual‐based networks involving a harvester ant, seeds, and invertebrates |
| Q57097149 | Structural refuges in two stem-boring weevils on Rumex crispus |
| Q57196927 | Structure and vertical stratification of plant galler-parasitoid food webs in two tropical forests |
| Q115432286 | Structure of two macrolepidopteran assemblages onSalix nigra(Marsh) andAcer negundoL.: abundance, diversity, richness, and persistence of scarce species |
| Q64216202 | Sublethal effect of brood parasitism on the grass-carrying wasp Isodontia mexicana |
| Q127902579 | Suboptimal oviposition of tephritid flies supports parasitoid wasps |
| Q117219571 | Substantial niche overlap in carrion beetle habitat and vegetation use |
| Q112169625 | Substrate moisture, particle size and temperature preferences of trap‐building larvae of sympatric antlions and wormlions from the rainforest of Borneo |
| Q115532928 | Suitability of woodlice prey for generalist and specialist spider predators: a comparative study |
| Q114081913 | Summer drought affects abundance of grassland grasshoppers differently along an elevation gradient |
| Q113272064 | Sunflower pollen reduces a gut pathogen in worker and queen but not male bumble bees |
| Q115405515 | Survivability and post-diapause fitness in a scolytid beetle as a function of overwintering developmental stage and the implications for population dynamics |
| Q59462508 | Survival, movement, and resource use of the butterfly Parnassius clodius |
| Q99967628 | Swarming behaviour in the Australian beetle, Heteronyx obesus, with notes on related species |
| Q105464087 | Switching roles from antagonist to mutualist: a harvester ant as a key seed disperser of a myrmecochorous plant |
| Q60270954 | Symbiont-conferred protection against Hymenopteran parasitoids in aphids: how general is it? |
| Q56169722 | Symbionts of societies that fission: mites as guests or parasites of army ants |
| Q125422185 | Synthesis and perspectives on the study of ant‐plant interaction networks: A global overview |
| Q125450779 | Systematic review of cuckoo bumblebee research reveals data gaps and understudied species |
| Q113282461 | Task-partitioned nectar transfer in stingless bees: work organisation in a phylogenetic context |
| Q113798278 | Taxonomic isolation and the accumulation of herbivorous insects: a comparison of introduced and native trees |
| Q112800887 | Taxonomic, functional, and phylogenetic perspectives on butterfly spatial assembly in northern Amazonia |
| Q56659868 | Temperate forest termites: ecology, biogeography, and ecosystem impacts |
| Q115531866 | Temperature and prey capture: opposite relationships in two predator taxa |
| Q56623545 | Temperature and the pollinating activity of social bees |
| Q115532925 | Temperature modulates the effects of predation and competition on mosquito larvae |
| Q123302562 | Temperature, deltamethrin‐resistance status and performance measures of Plutella xylostella: complex responses of insects to environmental variables |
| Q56980764 | Temperature-dependent reproduction of the spruce bark beetle Ips typographus, and analysis of the potential population growth |
| Q112800864 | Temporal and dietary niche is context‐dependent in tropical ants |
| Q111264024 | Temporal and geographic variation in parasitoid attack with no evidence for ant protection of the Melissa blue butterfly,Lycaeides melissa |
| Q61475639 | Temporal and spatial patterns in the emigrations of the army ant Dorylus (Anomma) molestus in the montane forest of Mt Kenya |
| Q128162155 | Temporal changes in the composition of parasitoid assemblages associated with the invasive chestnut gall wasp |
| Q122979896 | Temporal constancy in grasshopper assemblies (Orthoptera: Acrididae) |
| Q113173209 | Temporal patterns of seed use and availability in a guild of desert ants |
| Q60482999 | Temporal priority and intra-guild predation in temporary waters: an experimental study using Namibian desert dragonflies |
| Q57483662 | Temporal variation in body size and weapon allometry in the New Zealand giraffe weevil |
| Q36097047 | Ten years of invasion: Harmonia axyridis (Pallas) (Coleoptera: Coccinellidae) in Britain |
| Q125122824 | Termitariophily: expanding the concept of termitophily in a physogastric rove beetle (Coleoptera: Staphylinidae) |
| Q56380382 | Termite cohabitation: the relative effect of biotic and abiotic factors on mound biodiversity |
| Q113033982 | Testing competing hypotheses about the behaviour of floral visitors in mixed‐flower stands |
| Q111172606 | Testing effects of invasive fire ants and disturbance on ant communities of the longleaf pine ecosystem |
| Q36995994 | Testing for context-dependence in a processing chain interaction among detritus-feeding aquatic insects |
| Q56413702 | Testing the hypothesis of greater eurythermality in invasive than in native ladybird species: from physiological performance to life-history strategies |
| Q114081903 | Testing the migration syndrome: Comparative fecundity of migratory and non‐migratory nymphaline butterflies |
| Q113033926 | Testing the nutrition hypothesis for the adaptive nature of insect galls: does a non-adapted herbivore perform better in galls? |
| Q112810948 | Testing the resource concentration hypothesis with tarnished plant bug on strawberry: density of hosts and patch size influence the interaction between abundance of nymphs and incidence of damage |
| Q113033981 | Testing three hypotheses of rarity among the Buprestidae species of a tropical dry forest |
| Q115432305 | The Lepidoptera fauna associated with Calluna vulgaris: effects of plant architecture on abundance and diversity |
| Q54575950 | The adaptive and evolutionary significance of wing polymorphism and parthenogenesis in Ptinella Motschulsky (Coleoptera: Ptiliidae) |
| Q58924897 | The adaptive significance of male egg carrying in the golden egg bug: defining research avenues. A reply to Härdlinget al |
| Q115531880 | The arthropod predators of ant-mimetic and aposematic prey: a serological analysis |
| Q115532870 | The benefits of intraguild predation for a top predator spider |
| Q113798268 | The biogeography of herbivorous arthropods: species accrual on tropical crops |
| Q122713546 | The biology of the phonotactic parasitoid, Homotrixa sp. (Diptera: Tachinidae), and its impact on the survival of male Sciarasaga quadrata (Orthoptera: Tettigoniidae) in the field |
| Q55839331 | The community ecology of Aedes egg hatching: implications for a mosquito invasion |
| Q125893625 | The community‐wide and guild‐specific effects of pubescence on the folivorous insects of manzanitas Arctostaphylos spp. |
| Q122664738 | The complex hatching response of Aedes eggs to larval density |
| Q125360283 | The considerable adult size variability in wood feeders is optimal |
| Q58868496 | The cost of ant attendance and melezitose secretion in the black bean aphidAphis fabae |
| Q115531896 | The costs of reduced feeding due to predator avoidance: potential effects on growth and fitness in Ischnura elegans larvae (Odonata: Zygoptera) |
| Q56680632 | The degree of oligophagy in Locusta migratoria (L.) |
| Q125818810 | The deleterious effects of salinity stress on leafminers and their freshwater host |
| Q125416883 | The dispersal of microbes among and within flowers by butterflies |
| Q30048565 | The distribution and abundance of the British fungal-breeding Drosophila |
| Q57251345 | The distribution and decline of a widespread butterfly Lycaena phlaeas in a pastoral landscape |
| Q56918411 | The distribution and species characteristics of the Culicoides biting midge fauna of South Africa |
| Q126064834 | The distribution of a typhlocybine leafhopper, Ribautiana ulmi (Homoptera: Cicadellidae) on a specimen wych elm tree |
| Q111044117 | The distribution of risk and density-dependent mortality in the galls of Eurosta solidaginis, the goldenrod gall fly |
| Q113798279 | The distribution pattern of herbivory in a beech canopy |
| Q92097143 | The distribution, abundance and host plant relationships of Salix- feeding psyllids (Homoptera: Psylloidea) in arctic Alaska |
| Q115396424 | The diversity of Hymenoptera in the tropics with special reference to Parasitica in Sulawesi |
| Q57638017 | The dominant exploiters of the fig/pollinator mutualism vary across continents, but their costs fall consistently on the male reproductive function of figs |
| Q110615820 | The double cloak of invisibility: phenotypic plasticity and larval decoration in a geometrid moth,Synchlora frondaria, across three diet treatments |
| Q113798946 | The ecology and evolution of induced responses to herbivory and how plants perceive risk |
| Q123366190 | The effect of a foliar disease (rust) on the development of Gastrophysa viridula (Coleoptera: Chrysomelidae) |
| Q57601881 | The effect of colour variation in predators on the behaviour of pollinators: Australian crab spiders and native bees |
| Q56973235 | The effect of dispersal ability in winter and summer stoneflies on their genetic differentiation |
| Q59270555 | The effect of egg load and host deprivation on oviposition behaviour in aphidophagous hoverflies |
| Q57742182 | The effect of foundress number on sex ratio under partial local mate competition |
| Q57032217 | The effect of host developmental stage at parasitism on sex-related size differentiation in a larval endoparasitoid |
| Q60802294 | The effect of multi-species host density on superparasitism and sex ratio in a gregarious parasitoid |
| Q114145174 | The effect of prey density and host plant characteristics on oviposition and fertility in Anthocoris confusus (Reuter) |
| Q60546305 | The effect of rearing history and aphid density on volatile-mediated foraging behaviour of Diaeretiella rapae |
| Q57032354 | The effect of superparasitism on development of the solitary parasitoid wasp, Venturia canescens (Hymenoptera: Ichneumonidae) |
| Q121295122 | The effect of temperature and behaviour on the interaction between two dragonfly larvae species within the native and expanded range |
| Q125867607 | The effects of abiotically induced changes in host plant quality (and morphology) on a salt marsh planthopper and its parasitoid |
| Q113798247 | The effects of crop diversification on herbivorous insects: a meta-analysis approach |
| Q57426866 | The effects of drought and herbivory on plant-herbivore interactions across 16 soybean genotypes in a field experiment |
| Q57566803 | The effects of foliage damage on casebearing moth larvae, Coleophora serratella, feeding on birch |
| Q57262046 | The effects of foliar pubescence and nutrient enrichment on arthropod communities of Metrosideros polymorpha (Myrtaceae) |
| Q113181583 | The effects of foraging ants on arboreal insect herbivores in an undisturbed woodland savanna |
| Q126304283 | The effects of host plant species on adult oviposition and larval performance of the aphid predator Aphidoletes aphidimyza |
| Q57566825 | The effects of host-plant distribution and local abundance on the species richness of agromyzid flies attacking British umbellifers |
| Q56796841 | The effects of parasitoid fecundity and host taxon on the biological control of insect pests: the relationship between theory and data |
| Q60566042 | The effects of starvation and repeated disturbance on mass loss, pit construction, and spatial pattern in a trap-building predator |
| Q113271262 | The effects of temperature and body size on the mating pattern of a gregariously nesting bee, Colletes cunicularius (Hymenoptera: Colletidae) |
| Q125993334 | The effects of temperature and prey density on the development rates and growth of damselfly larvae (Odonata: Zygoptera) |
| Q56936993 | The effects of the invasive Argentine ant (Linepithema humile) and the native antPrenolepis imparison the structure of insect herbivore communities on willow trees (Salix lasiolepis) |
| Q115555386 | The escape response of pea aphids to foliar-foraging predators: factors affecting dropping behaviour |
| Q56854550 | The evolution of parental care in insects: the roles of ecology, life history and the social environment |
| Q56112645 | The evolutionary ecology of cheating: does superficial oviposition facilitate the evolution of a cheater yucca moth? |
| Q60562759 | The farming ant Sericomyrmex amabilis nutritionally manages its fungal symbiont and its social parasite |
| Q99975682 | The first parasitic Trichoptera |
| Q113798949 | The forgotten season: the impact of autumn phenology on a specialist insect herbivore community on oak |
| Q57265264 | The frequency of multi-queen colonies increases with altitude in a Nearctic ant |
| Q115396437 | The function of multiple anti-predator mechanisms in adult tiger beetles (Coleoptera: Cicindelidae) |
| Q115396457 | The function of turret building behaviour in the larval tiger beetle, Cicindela willistoni (Coleoptera: Cicindelidae) |
| Q115531887 | The growth and survival of Panolis flammea larvae in the absence of predators on Scots pine and lodgepole pine |
| Q122451040 | The hatching stimulus for eggs of Aedes punctor (Diptera: Culicidae) |
| Q112798878 | The impact of altered precipitation on spatial stratification and activity-densities of springtails (Collembola) and spiders (Araneae) |
| Q111263880 | The impact of an ant-aphid mutualism on the functional composition of the secondary parasitoid community |
| Q56774951 | The impact of an exotic social wasp (Vespula germanica) on the native arthropod community of north-west Patagonia, Argentina: an experimental study |
| Q115396450 | The impact of forest cutting on the diversity of ground beetles (Coleoptera: Carabidae) in the southern Appalachians |
| Q117705398 | The impact of wildfire and mammal carcasses on beetle emergence from heathland soils |
| Q57008001 | The impacts of predators and parasites on wild bumblebee colonies |
| Q111493075 | The importance of canopy complexity in shaping seasonal spider and beetle assemblages in saltmarsh habitats |
| Q62377127 | The importance of specialist natural enemies for Chrysomela lapponica in pioneering a new host plant |
| Q113855250 | The influence of ants and water availability on oviposition behaviour and survivorship of a facultatively ant‐tended herbivore |
| Q61996360 | The influence of different spatial-scale variables on caddisfly assemblages in Flemish lowland streams |
| Q56699261 | The influence of habitat use and foraging on the replacement of one introduced wasp species by another in New Zealand |
| Q115432273 | The influence of host plant diversity and food quality on larval survival of plant feeding heteropteran bugs |
| Q129184362 | The influence of light environment on host colour preference in a parasitoid wasp |
| Q60531691 | The influence of prior experience on preference and performance of a cryptoparasitoidScleroderma guani(Hymenoptera: Bethylidae) on beetle hosts |
| Q56776524 | The influence of temperature and fine-scale resource distribution on resource sharing and domination in an ant community |
| Q113173496 | The interactive effects of climate, life history, and interspecific neighbours on mortality in a population of seed harvester ants |
| Q113855243 | The interplay between plant traits and herbivore attack: a study of a stem galling midge in the neotropics |
| Q56384448 | The life and death of barn beetles: faunas from manure and stored hay inside farm buildings in northern Iceland |
| Q54666515 | The life history of Philanisus plebeius Walker (Trichoptera: Chathamiidae), a caddisfly whose eggs were found in a starfish |
| Q112852029 | The macroevolution of climatic niches and its role in ant diversification |
| Q56883202 | The metazoan food webs from six Bornean Nepenthes species |
| Q125476043 | The missing links: Bee and non‐bee alpine visitor observation networks differ to pollen transport networks |
| Q56212600 | The nature of migration in the red admiral butterfly Vanessa atalanta: evidence from the population ecology in its southern range |
| Q112800893 | The network structure of myrmecophilic interactions |
| Q113855232 | The occurrence and effectiveness of hypersensitive reaction against galling herbivores across host taxa |
| Q125477024 | The occurrence of sequential oviposition in fig wasps and the implications for interpreting sex ratio data |
| Q109009047 | The origins of northern European Autographa gamma individuals evaluated using hydrogen stable isotopes |
| Q56785111 | The pea aphid complex as a model of ecological speciation |
| Q124839436 | The population dynamics of the yellow crazy ant Anoplolepis gracilipes (Hymenoptera: Formicidae) on a tropical island in Malaysia |
| Q56780845 | The potential impacts of the arrival of the harlequin ladybird, Harmonia axyridis (Pallas) (Coleoptera: Coccinellidae), in Britain |
| Q125622780 | The power and efficiency of brood incubation in queenless microcolonies of bumble bees (Bombus terrestris L.) |
| Q115531882 | The predators of insects |
| Q58423766 | The presence of conifer resin decreases the use of the immune system in wood ants |
| Q56987607 | The relationship between egg load and fecundity among Trichogramma parasitoids |
| Q56785107 | The relationship between feeding specialization and host plants to aldrin epoxidase activities of midgut homogenates in larval Lepidoptera |
| Q111247967 | The relationship between the abundances of bumblebees and honeybees in a native habitat |
| Q99966956 | The repair of larval cells and other larval activities in Geotrupes spiniger Marsham and other species (Coleoptera, Scarabaeidae) |
| Q111264009 | The resource‐mediated modular structure of a non‐symbiotic ant–plant mutualism |
| Q56987594 | The response of Hyssopus pallidus to hosts previously parasitised by Ascogaster quadridentata: heterospecific discrimination and host quality |
| Q125406178 | The response to fire by two eusocial bee species |
| Q115531897 | The responses of polyphagous predators to prey spatial heterogeneity: aggregation by carabid and staphylinid beetles to their cereal aphid prey |
| Q125993377 | The role of body size in mating success of Sphenarium purpurascens in Central Mexico |
| Q125289623 | The role of carrion‐frequenting arthropods in the decay process |
| Q113798256 | The role of extrafloral nectaries in Qualea grandiflora (Vochysiaceae) in limiting herbivory: an experiment of ant protection in cerrado vegetation |
| Q113798266 | The role of extrafloral nectaries in the herbivore defence of Cassia fasiculata |
| Q113271261 | The role of larval nutrition in pre-imaginal biasing of caste in the primitively eusocial wasp Ropalidia marginata (Hymenoptera: Vespidae) |
| Q126165252 | The role of olfactory stimuli in the location of weakened hosts by twig‐infesting Pityophthorus spp. |
| Q114145176 | The role of predator-prey size ratio in determining the efficiency of capture by Anthocoris nemorum and the escape reactions of its prey, Acyrthosiphon pisum |
| Q113855229 | The role of resources and natural enemies in determining the distribution of an insect herbivore population |
| Q60487756 | The role of temperature in competition and persistence of an invaded ant assemblage |
| Q36141400 | The role of the North Atlantic Oscillation in controlling U.K. butterfly population size and phenology |
| Q56551793 | The roles and interactions of reproductive isolation mechanisms in fall armyworm (Lepidoptera: Noctuidae) host strains |
| Q56880097 | The roles of history: age and prior exploitation in aquatic container habitats have immediate and carry-over effects on mosquito life history |
| Q110615268 | The roles of phenotypic plasticity and adaptation in morphology and performance of an invasive species in a novel environment |
| Q115532950 | The roles of top and intermediate predators in herbivore suppression: contrasting results from the field and laboratory |
| Q114145173 | The searching behaviour of Anthocoris confusus (Reuter) in relation to prey density and plant surface topography |
| Q57039015 | The seasonal dynamic of ant-flower networks in a semi-arid tropical environment |
| Q57200013 | The seasonality of arboreal arthropods foraging within an Australian rainforest tree |
| Q58855339 | The significance of a facultative bacterium to natural populations of the pea aphid Acyrthosiphon pisum |
| Q56267944 | The significance of prey in the diet of the phytophagous thrips, Frankliniella schultzei |
| Q56453626 | The size-distance relationship in the wood ant Formica rufa |
| Q113036785 | The size-grain hypothesis: a phylogenetic and field test |
| Q113033927 | The size?grain hypothesis: do macroarthropods see a fractal world? |
| Q113033989 | The slow-growth high-mortality hypothesis: direct experimental support in a leafmining fly |
| Q125774497 | The spatial distribution of beetles within the canopies of oak trees in Richmond Park, U.K. |
| Q111493057 | The structure of the aquatic insect community associated with intertidal pools on a New Jersey salt marsh |
| Q56927676 | The tethered flight technique as a tool for studying life-history strategies associated with migration in insects |
| Q115532922 | The three criteria for resistance by plant carrion-provisioning: insect entrapment and predator enrichment onMimulus bolanderi |
| Q111172590 | The three‐dimensional macronutrient niche of an invasive generalist predator |
| Q60506541 | The time and egg budget of Leptopilina clavipes, a parasitoid of larval Drosophila |
| Q113389134 | The upper thermal tolerance for a Texas population of the hairy maggot blow flyChrysomya rufifaciesMacquart (Diptera: Calliphoridae) |
| Q56031724 | The use of chemical composition as a population marker in insects: a study of the Brimstone butterfly |
| Q58417539 | The use of digital video recorders in pollination biology |
| Q113282460 | The use of field-based social information in eusocial foragers: local enhancement among nestmates and heterospecifics in stingless bees |
| Q61761929 | The use of oviposition-induced plant cues by Trichogramma egg parasitoids |
| Q67311516 | The usefulness of destructive host feeding parasitoids in classical biological control: theory and observation conflict |
| Q114106536 | The utilization of patchy thermal microhabitats by the ectothermic insect predator, Cicindela sexguttata |
| Q57241967 | The value of georeferenced collection records for predicting patterns of mosquito species richness and endemism in the Neotropics |
| Q54586297 | The volatile organic compounds of introduced and native dung and carrion and their role in dung beetle foraging behaviour |
| Q125659795 | The ‘night shift’: nocturnal pollen-transport networks in a boreal pine forest |
| Q60233856 | Thermal change alters the outcome of behavioural interactions between antagonistic partners |
| Q60531266 | Thermal tolerance and recovery behaviour of Thorectes lusitanicus (Coleoptera, Geotrupidae) |
| Q113033987 | Thermal tolerance varies with dim‐light foraging and elevation in large carpenter bees (Hymenoptera: Apidae: Xylocopini) |
| Q42590329 | Thermoregulation of foraging honeybees on flowering plants: seasonal variability and influence of radiative heat gain |
| Q57196960 | Three ways of assessing metapopulation structure in the butterfly Plebejus argus |
| Q115555369 | Tigers eating tigers: evidence of intraguild predation operating in an assemblage of tiger beetles |
| Q121793227 | Time-lags in insect response to plant productivity: significance for plant-insect interactions in deserts |
| Q126080254 | Timing is everything? Phenological synchrony and population variability in leaf‐chewing herbivores of Quercus |
| Q60572395 | Timing of diapause induction and its life-history consequences in Nezara viridula: is it costly to expand the distribution range? |
| Q56996103 | To be an intra-guild predator or a cannibal: is prey quality decisive? |
| Q57607636 | To be or not to be faithful: flexible fidelity to foraging trails in the leaf-cutting ant Acromyrmex lobicornis |
| Q60438845 | Towards an understanding of how phloem amino acid composition shapes elevated CO2-induced changes in aphid population dynamics |
| Q57043622 | Towards an understanding of the mechanisms of tolerance: compensating for herbivore damage by enhancing a mutualism |
| Q125995787 | Tracking larval insect movement within soil using high resolution X‐ray microtomography |
| Q115531857 | Tracking predator density dependence and subterranean predation by carabid larvae on slugs using monoclonal antibodies |
| Q57308617 | Trade-off between mobility and fitness in Cydia pomonella L. (Lepidoptera: Tortricidae) |
| Q115405404 | Trade‐off mediated by pyrrolizidine alkaloids predicts alternative reproductive tactics in ithomiine butterflies |
| Q115555384 | Trail sex pheromone as a cue for searching mates in an insect predator Orius sauteri |
| Q115531785 | Trait-mediated effects of predation across life-history stages in container mosquitoes |
| Q113272069 | Traits reveal ecological strategies driving carrion insect community assembly |
| Q113798926 | Trait‐based characterisation of parasitoid wasp communities in natural and agricultural areas |
| Q125636600 | Transgenerational developmental effects of species‐specific, maternally transmitted microbiota in Onthophagus dung beetles |
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