about
Deep mtDNA divergences indicate cryptic species in a fig-pollinating waspObligate mutualism within a host drives the extreme specialization of a fig wasp genomeAn extreme case of plant-insect codiversification: figs and fig-pollinating wasps.60 million years of co-divergence in the fig-wasp symbiosisLifecycle closure, lineage sorting, and hybridization revealed in a phylogenetic analysis of European oak gallwasps (Hymenoptera: Cynipidae: Cynipini) using mitochondrial sequence data.Interference competition and high temperatures reduce the virulence of fig wasps and stabilize a fig-wasp mutualismA role for parasites in stabilising the fig-pollinator mutualism.Host niches and defensive extended phenotypes structure parasitoid wasp communitiesUnravelling mummies: cryptic diversity, host specificity, trophic and coevolutionary interactions in psyllid - parasitoid food webs.Molecular species delimitation of a symbiotic fig-pollinating wasp species complex reveals extreme deviation from reciprocal partner specificityChaos of Wolbachia sequences inside the compact fig syconia of Ficus benjamina (Ficus: moraceae).Phylogeny, biogeography, and ecology of Ficus section Malvanthera (Moraceae).Double trouble: combined action of meiotic drive and Wolbachia feminization in Eurema butterflies.Codivergence of the primary bacterial endosymbiont of psyllids versus host switches and replacement of their secondary bacterial endosymbionts.Ant Larval Demand Reduces Aphid Colony Growth Rates in an Ant-Aphid Interaction.Figs and fig wasps.Local coexistence and genetic isolation of three pollinator species on the same fig tree species.The Curious Case of the Camelthorn: Competition, Coexistence, and Nest-Site Limitation in a Multispecies Mutualism.Longevity, early emergence and body size in a pollinating fig wasp--implications for stability in a fig-pollinator mutualism.Cryptic diversity in a fig wasp community-morphologically differentiated species are sympatric but cryptic species are parapatric.A trophic cascade induced by predatory ants in a fig-fig wasp mutualism.High nymphal host density and mortality negatively impact parasitoid complex during an insect herbivore outbreak.Fossil-calibrated molecular phylogenies reveal that leaf-mining moths radiated millions of years after their host plants.The evolution of host use and unusual reproductive strategies in Achrysocharoides parasitoid wasps.Diverse Mariner-like elements in fig wasps.Sex determination and population biology in the hymenoptera.Wolbachia infection and dramatic intraspecific mitochondrial DNA divergence in a fig wasp.Macroevolutionary patterns in the origin of mutualisms involving ants.Relative Abundance and Strain Diversity in the Bacterial Endosymbiont Community of a Sap-Feeding Insect Across Its Native and Introduced Geographic Range.Extreme host plant conservatism during at least 20 million years of host plant pursuit by oak gallwasps.The discovery of Halictivirus resolves the Sinaivirus phylogeny.One step ahead: a parasitoid disperses farther and forms a wider geographic population than its fig wasp host.Convergent structure of multitrophic communities over three continents.The global phylogeny of the subfamily Sycoryctinae (Pteromalidae): parasites of an obligate mutualism.Molecular dating and biogeography of fig-pollinating wasps.Chemical camouflage: a key process in shaping an ant-treehopper and fig-fig wasp mutualistic network.A comparative study of virginity in fig waspsAnt semiochemicals limit apterous aphid dispersal.Evolution of a complex coevolved trait: active pollination in a genus of fig wasps.Brood sex ratio variance, developmental mortality and virginity in a gregarious parasitoid wasp.
P50
Q21283950-8C1D88EB-A0BD-45FE-8687-B5D48B8F387FQ28658356-191850EB-0E2B-4005-AE6F-E5D79963992EQ28715729-91AA8059-A5B0-40AB-B6F8-60D506B358ACQ28767983-BFD7C1BE-D919-494B-9ACA-79900D438631Q30753201-B8E11048-E1B9-498C-8F63-AE424BF2E785Q30885925-541A7580-040E-4ACA-8E2A-BA43667D7C39Q33323450-FDC224D3-AC5C-42CB-97FA-5C723EBF153DQ33496687-00C2C126-2F54-4010-A1C4-EED191C5E37AQ33771485-6DBA747D-2675-447B-B8F1-688138038567Q34233370-E9A79233-34C9-44A8-99C1-2CA87A28A224Q34473661-D1942EC5-032E-415E-A165-6947C95DDC2CQ34779677-C80ABBE0-9E0A-4960-8FEF-8E71E7AACD08Q35683566-423D077A-E634-4B5E-8A5A-0765DDD8A980Q35999046-12B4C53A-4C40-4A16-ABD8-FBB34D1DFD9EQ36007646-EE20D6E9-3177-496C-9053-5C0FC5908226Q36345075-02B0801A-C132-4A27-93FD-54AB9FA47FC9Q38771992-9A74D741-6569-485F-B0CF-87EE64F68AF5Q38933209-311EE299-69C6-4A65-AC3B-F20516CA2111Q38979849-AAB888D3-BF63-41D2-BA0D-48137AFB55A9Q39062487-98F6691D-7A37-445C-890A-AD27ABFA2A59Q39572352-8C28AA65-4AEA-4264-913C-A92BD6A1454DQ40069684-22DA5B81-9726-4381-936C-C5F7E0FBBAE2Q42036997-D2DF3878-0FA4-449F-BA02-EB35BBF85FA6Q42040306-C3BAEABE-FDDB-4BC8-8B4A-A97D15402A49Q42640372-F03A50DD-797D-4BF8-A33A-EE264FBEA0ABQ43793045-DADA6C28-55BD-4FE0-B553-38883C2750BFQ45151177-0176F100-E80C-4E6F-988C-FEF957FDF44AQ45746788-3BB1806A-6985-4F45-B939-CCCAC05C1E69Q45881218-9717EE6C-CC0F-464E-BB51-45022B94914DQ46085395-C9DDD777-9229-4212-9449-48FEE9C2BE47Q46277586-261D22F5-9C56-435F-97EF-1462592F70ABQ46596089-5723883C-F60D-48B7-AFA8-F09408B5FBB3Q46981605-F8E7F2F8-FB43-4C19-9177-BAAE65698147Q47241618-3BC7BAB3-2BB4-40B4-9E15-1AA24C15EAA1Q47271449-8C4B1BC0-A115-4ACA-A33C-0168E20B4D45Q48138511-6180EA7A-BDC9-4227-BA4F-03E80CB64A86Q50939373-D9EE5D06-57DA-4D11-8E63-A3BC4D43B3AAQ51975502-A99048C2-2094-4DFA-9E39-8DF51B2C236CQ52001784-4D3DC9C7-2231-47C4-BE15-A1211C983971Q52206664-958CF049-43BC-4644-AFBF-947DEF6CCE08
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
James M Cook
@ast
James M Cook
@en
James M Cook
@es
James M Cook
@nl
James M Cook
@sl
جيمس سانتشيز كوك
@ar
type
label
James M Cook
@ast
James M Cook
@en
James M Cook
@es
James M Cook
@nl
James M Cook
@sl
جيمس سانتشيز كوك
@ar
prefLabel
James M Cook
@ast
James M Cook
@en
James M Cook
@es
James M Cook
@nl
James M Cook
@sl
جيمس سانتشيز كوك
@ar
P108
P1053
D-6423-2011
P106
P21
P31
P3829
P496
0000-0001-8447-6126