about
The effect of geographic range on extinction risk during background and mass extinctionA shift in the long-term mode of foraminiferan size evolution caused by the end-Permian mass extinctionThe influence of the biological pump on ocean chemistry: implications for long-term trends in marine redox chemistry, the global carbon cycle, and marine animal ecosystemsLimited role of functional differentiation in early diversification of animalsMetabolic dominance of bivalves predates brachiopod diversity decline by more than 150 million yearsLong-term differences in extinction risk among the seven forms of raritySize-frequency distributions along a latitudinal gradient in Middle Permian fusulinoideansCalcium isotope constraints on the end-Permian mass extinctionTwo-phase increase in the maximum size of life over 3.5 billion years reflects biological innovation and environmental opportunityLarge perturbations of the carbon cycle during recovery from the end-permian extinction.Animal evolution. Cope's rule in the evolution of marine animals.Marine anoxia and delayed Earth system recovery after the end-Permian extinction.Ecological selectivity of the emerging mass extinction in the oceans.Extinction intensity, selectivity and their combined macroevolutionary influence in the fossil recordThe evolutionary consequences of oxygenic photosynthesis: a body size perspective.Late paleozoic fusulinoidean gigantism driven by atmospheric hyperoxia.Constraints on the adult-offspring size relationship in protists.Body size downgrading of mammals over the late Quaternary.Hierarchical complexity and the size limits of life.Phanerozoic pO2 and the early evolution of terrestrial animals.Paleophysiology and end-Permian mass extinctionTemperature-dependent hypoxia explains biogeography and severity of end-Permian marine mass extinctionGlobal Perturbation of the Marine Calcium Isotope Cycle During the Permian-Triassic TransitionEcologically diverse clades dominate the oceans via extinction resistanceA Cretaceous peak in family-level insect diversity estimated with mark-recapture methodologyPhysiological constraints on body size distributions in Crocodyliformes
P50
Q22066351-A6BF4DFD-9124-4987-8C88-649A2CA5CA9CQ28286623-8F7861E4-50E6-4375-9962-8F29CF2A16C3Q28597218-63279A9A-9FF0-431B-9FB3-75438E777063Q28652163-8027783E-B790-4A2E-8EC0-2E67310EDA93Q28658466-44070D72-42F3-44D6-816D-E1803963795BQ28713158-FDEE5FD5-50FF-4CCB-A329-5DD200AB213AQ28728739-F98694CA-985B-40B1-B396-2FBBED4AB32FQ28751339-8A4B6662-1090-4468-851A-83443B96C09BQ28756066-816E096B-A216-46AA-9932-0F60BB6ACF14Q30834306-F16A08AE-B898-47E4-9CCE-DF748B1A651CQ34463839-E54AF257-2239-406C-9896-C031D3B345B2Q34514444-6FB9DE3B-411D-4276-BE75-8EC697525755Q34540320-49E7307F-2581-43A5-92EB-1ABF4EDC1BF7Q36160998-2096E8F9-F7D0-4EE7-85A3-29B459F2CFB7Q37785859-61F3FD08-E238-4774-B132-C975B061484FQ46094456-5C1B8CCC-3B0A-4C15-9B7D-C019CB479B53Q46964292-9130770E-D226-415F-B7E2-BA8ED084B021Q52576498-7A0D3ACA-E6DB-437C-A541-AC6913B9F43DQ52598760-F770064A-86B3-41C9-A037-766726F93959Q52706048-90D9E375-4894-4FED-AA0C-EC1AE02DDDEDQ55898881-a53f794a-4a4a-0f7e-7124-c819cfed1a66Q59508802-E0AAD4A6-3CD5-4F66-A257-D122848A1A69Q66692312-37c5fc29-45d7-2b67-cc32-66d4b49a5015Q89930343-837355BC-9B7C-434E-B1D9-7A395F8233B8Q92054408-1EEC993F-2F5F-4BE0-8D5B-12B2029BBC60Q92675535-12C2514B-75BE-4CD4-930A-0677E068A2E2
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jonathan L Payne
@nl
Jonathan L Payne
@sl
Jonathan L. Payne
@en
Jonathan L. Payne
@es
type
label
Jonathan L Payne
@nl
Jonathan L Payne
@sl
Jonathan L. Payne
@en
Jonathan L. Payne
@es
prefLabel
Jonathan L Payne
@nl
Jonathan L Payne
@sl
Jonathan L. Payne
@en
Jonathan L. Payne
@es
P106
P244
P1053
A-1240-2007
P1153
7403333496
P21
P244
no2014003284
P31
P3829
P496
0000-0002-9601-3310