about
Differential phenotypic and genetic expression of defence compounds in a plant-herbivore interaction along elevationPlate tectonics drive tropical reef biodiversity dynamicsPhylogenetic plant community structure along elevation is lineage specificThe role of biotic interactions in shaping distributions and realised assemblages of species: implications for species distribution modellingTrophic specialization influences the rate of environmental niche evolution in damselfishes (Pomacentridae)Thermal niches are more conserved at cold than warm limits in arctic-alpine plant species.Forecasted coral reef decline in marine biodiversity hotspots under climate change.Loss of connectivity among island-dwelling Peary caribou following sea ice decline.Predicting present and future intra-specific genetic structure through niche hindcasting across 24 millennia.Shifts in species richness, herbivore specialization, and plant resistance along elevation gradientsCombining food web and species distribution models for improved community projections.Airborne and Grain Dust Fungal Community Compositions Are Shaped Regionally by Plant Genotypes and Farming Practices.Density-based hierarchical clustering of pyro-sequences on a large scale--the case of fungal ITS1.Plant species distributions along environmental gradients: do belowground interactions with fungi matter?Combining modelling tools to evaluate a goose management scheme.Social structure varies with elevation in an Alpine ant.Turnover of plant lineages shapes herbivore phylogenetic beta diversity along ecological gradients.Horizontal, but not vertical, biotic interactions affect fine-scale plant distribution patterns in a low-energy system.Species pool distributions along functional trade-offs shape plant productivity-diversity relationships.Comparing species interaction networks along environmental gradients.Different rates of defense evolution and niche preferences in clonal and nonclonal milkweeds (Asclepias spp.).Morphological, ecological and genetic aspects associated with endemism in the Fly Orchid group.Transitions in social complexity along elevational gradients reveal a combined impact of season length and development time on social evolution.The unfolding of plant growth form-defence syndromes along elevation gradients.Climatic niche evolution is faster in sympatric than allopatric lineages of the butterfly genus Pyrgus.Temporally dynamic habitat suitability predicts genetic relatedness among caribou.Comparing spatial diversification and meta-population models in the Indo-Australian Archipelago.Biological introduction risks from shipping in a warming ArcticMeasuring ecological niche overlap from occurrence and spatial environmental dataThe simultaneous inducibility of phytochemicals related to plant direct and indirect defences against herbivores is stronger at low elevationHerbicide and fertilizers promote analogous phylogenetic responses but opposite functional responses in plant communitiesDisentangling the processes driving plant assemblages in mountain grasslands across spatial scales and environmental gradientsImproving spatial predictions of taxonomic, functional and phylogenetic diversityCommunity-level plant palatability increases with elevation as insect herbivore abundance declinesUneven rate of plant turnover along elevation in grasslandsPast climate-driven range shifts and population genetic diversity in arctic plantsSimulated shifts in trophic niche breadth modulate range loss of alpine butterflies under climate changeThe regional species richness and genetic diversity of Arctic vegetation reflect both past glaciations and current climateUsing species richness and functional traits predictions to constrain assemblage predictions from stacked species distribution modelsGenetic diversity in caribou linked to past and future climate change
P50
Q28598170-836DA47D-C455-4CD0-8E6E-29731955F410Q28603147-C90E3358-8227-45D2-9DEC-C266629032D1Q28660605-592CA5CB-CDE5-419E-A006-56BB44E4B770Q28709304-3B0FEE97-843B-4B9F-906C-EB03AD479464Q28728512-D5BFFDD2-6C40-4FBC-82E2-54A6CAC7A092Q30813305-2AA6F4BC-A87B-462F-90FB-55EDB153AAE4Q30885582-CE30672C-2D0D-44A3-AE75-421941516A4BQ31132076-3965FAF8-1E1B-4D69-A0E7-FED446DCAA3DQ34239460-1EAE704C-1663-4172-B6EF-321419EDAA40Q34408348-2AB681CD-EBEC-4DC8-936B-6C99F4ED4D6BQ35068090-2D0CD947-ADEC-4954-8717-E6E666A63864Q35908818-84E45D3D-33E2-4D15-AA01-01FF5A74C1B1Q36846162-8DB3BC35-5621-4BBF-A41F-CD7675EFD8AFQ37379164-CB6C7CF3-790B-46C3-9671-66485D9A2ADAQ37651274-E5450756-A9A0-4FE2-A0A5-81F4D3039FC7Q41673030-3F114C76-AB27-48A2-A4D2-53A9BE105FA0Q43407403-43C5088E-5F7B-4EF3-B702-411001F24C85Q43995682-C74FDCAA-6603-4FE9-B5BF-20B563755FC9Q46262346-E0DBDEAC-AA36-44CC-ADF9-4BBC6E7EC1E8Q46302118-22132A6E-6ADC-43A3-A6A3-5BB95DBC4C2FQ46668149-293C9606-3C0F-451D-9F80-E9566E916A50Q48041272-70A70754-0EED-4E7A-AD3C-7AFD97605B87Q51083169-AF394117-1EF7-428D-B861-072ACF9679A0Q51150902-9B194B86-F94B-4616-A2CF-8980BFBC1769Q51216225-FE9E5C20-3EBF-4059-8AB6-EB0F91A9A2C3Q51419122-FCC09DE5-ADA9-4E82-B842-5F548B013819Q53830115-7B2C6188-A39A-496F-9ECF-162B2C355F1CQ56414608-31067103-7085-4F70-B5DB-52A3EB196ED7Q56567714-B59C9339-82E3-4ED1-9C08-B69EF20F5135Q56998817-AA31187D-7ACE-4158-B5BB-C7CBDD233710Q56999336-66AD7AF1-C45F-4E5C-BC88-5DAF61377C4FQ57013692-0D309ABE-B066-4CC0-9B57-4C49280F548BQ57013702-8AB81943-5118-4B9D-99D4-D9CC9FF21311Q57013710-666D822A-0926-4693-A402-214DA1E4A8AEQ57013730-2F587C6D-78A1-4380-83C8-A55FBBD1DD9DQ57013756-982F2CF4-452E-451D-81DA-78C3B642B702Q57013759-E07513B1-2BE0-4834-BC8D-805C75BED18BQ57013772-FB64A68B-88CF-4963-8828-E5D631EE815FQ57013859-F17707F1-07D6-46AA-A1A6-B2E323C9E7ABQ57013881-A8939C84-9BBF-4025-95CC-EC7FFDAC0560
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Loïc Pellissier
@ast
Loïc Pellissier
@en
Loïc Pellissier
@es
Loïc Pellissier
@nl
Loïc Pellissier
@sl
type
label
Loïc Pellissier
@ast
Loïc Pellissier
@en
Loïc Pellissier
@es
Loïc Pellissier
@nl
Loïc Pellissier
@sl
prefLabel
Loïc Pellissier
@ast
Loïc Pellissier
@en
Loïc Pellissier
@es
Loïc Pellissier
@nl
Loïc Pellissier
@sl