about
Persistence and change in community composition of reef corals through present, past, and future climatesHosts of the Plio-Pleistocene past reflect modern-day coral vulnerabilityHuman deforestation outweighs future climate change impacts of sedimentation on coral reefs.Community change and evidence for variable warm-water temperature adaptation of corals in Northern Male Atoll, Maldives.Coral reefs: corals' adaptive response to climate change.Biogeography and change among regional coral communities across the Western Indian OceanA comparison of marine protected areas and alternative approaches to coral-reef management.Climate warming, marine protected areas and the ocean-scale integrity of coral reef ecosystems.Identifying reefs of hope and hopeful actions: contextualizing environmental, ecological, and social parameters to respond effectively to climate change.Crucial knowledge gaps in current understanding of climate change impacts on coral reef fishes.Relationship between historical sea-surface temperature variability and climate change-induced coral mortality in the western Indian Ocean.West Indian Ocean variability and East African fish catch.Transitional states in marine fisheries: adapting to predicted global change.Extinction vulnerability of coral reef fishes.Global gradients of coral exposure to environmental stresses and implications for local management.Critical thresholds and tangible targets for ecosystem-based management of coral reef fisheries.To fish or not to fish: factors at multiple scales affecting artisanal fishers' readiness to exit a declining fishery.Comparison of marine spatial planning methods in Madagascar demonstrates value of alternative approachesAssessing gear modifications needed to optimize yields in a heavily exploited, multi-species, seagrass and coral reef fishery.Marine reserves as linked social-ecological systemsEvaluating life-history strategies of reef corals from species traits.Life histories predict coral community disassembly under multiple stressors.Rebuilding global fisheries.Recovery potential of the world's coral reef fishes.Evaluating taboo trade-offs in ecosystems services and human well-beingTrophic cascades result in large-scale coralline algae loss through differential grazer effects.Biomass-based targets and the management of multispecies coral reef fisheries.Malthusian overfishing and efforts to overcome it on Kenyan coral reefs.Linking ecosystem services and human-values theory.Algal growth and species composition under experimental control of herbivory, phosphorus and coral abundance in Glovers Reef, Belize.Redistribution of benefits but not detection in a fisheries bycatch-reduction management initiative.Response of the coral reef benthos and herbivory to fishery closure management and the 1998 ENSO disturbance.Socioeconomic factors that affect artisanal fishers' readiness to exit a declining fishery.Data-driven models for regional coral-reef dynamics.Comparing bleaching and mortality responses of hard corals between southern Kenya and the Great Barrier Reef, Australia.Effects of fisheries closures and gear restrictions on fishing income in a Kenyan coral reef.Coexistence in a sea urchin guild and its implications to coral reef diversity and degradation.Comparison of modern and historical fish catches (AD 750-1400) to inform goals for marine protected areas and sustainable fisheries.Echinoid bioerosion and herbivory on Kenyan coral reefs: the role of protection from fishing.Phosphorus and nitrogen effects on microbial euendolithic communities and their bioerosion rates.
P50
Q28655132-2F16155D-9AC1-4470-BD9A-097CA818BD76Q28730007-0341F73E-5033-43C2-9756-B3D07BE7AE7FQ30640750-B1B596E5-7A33-40D1-840C-2972FE08AE0AQ30746574-6ECE37FF-C348-4F0B-9247-326B56EB2EF0Q30766954-ADBBDA14-6B8D-4244-AD89-F8523A71B730Q30797567-AA8827F6-E201-41AF-A76B-5CB0CDD15A02Q33251409-25BECFFE-7C8D-44CC-A22E-1B1F4F63C515Q33363554-8D0912B7-F6C4-4626-AEAB-94A486E5148BQ33412850-1244E351-B82C-478A-825D-DC5AAEED4B7BQ33535138-1275C0C0-4265-4FD9-A923-8C758B6756E6Q33571892-ACFB5E1F-35D1-4CBC-8654-0C2F20C6B6B8Q33578686-E1746CB1-74DE-4C98-9DD7-24EEBF48BEB6Q33730041-D11729A7-F9FB-401A-A960-65A087A1B739Q33820170-1DE5B572-B28D-490A-9DBF-D00B9899F561Q34000849-F2E7E00D-184D-4485-9E01-DB69457E1288Q34031080-09C4617C-C806-4E52-A860-0FF51E6F437AQ34163556-CA401D70-D906-49BC-BC4E-BEADB12862A2Q34167976-108D64C0-68A1-4D78-ACEE-B3C910DB5EF5Q34264566-68CACBFC-82CF-4773-B494-DD8EA09FEEF0Q34276517-246A5894-ABD7-4AB0-A164-AFB101BFFA45Q34400222-304987EB-3140-4E0E-8E66-A857C8E7C03EQ34625090-2A08E916-1788-461F-8EA3-0BAB97A49655Q34994863-E5126CAA-F7DF-4CBF-976D-8F584F47E0C2Q35597886-7C497B70-2A2C-4F1E-8682-CEA5146F2497Q35699275-D7ADEC26-37B3-4669-BFE3-EC7615693472Q39286326-C1AA26EF-832B-405B-A6FF-9F9D3B49B5CDQ41705662-326337E7-A60E-4329-B0E3-4D7CE3896A28Q45776411-71473E61-F441-4B5B-B644-A3C35A1FAD60Q46203162-FF2535DD-5CA1-4EB0-9202-3E4B9BF066CDQ46205943-8C72D87B-9716-4D24-AD30-CADAB074BDF6Q46220432-FBDEA05C-3ECE-466D-8FAD-D9FED7B47CAFQ46313121-BF15176D-5487-4805-A1C6-DD0F70D5251BQ46332329-32CAFCA8-172A-4684-AF54-CBC301499E97Q46424526-CD4CA56B-9E96-49CF-ABA5-B589FDA06608Q46426398-CF2A3831-7DD7-4DB7-B641-AABFC40EC6C4Q46784272-D8989DFA-E7E9-459C-83C0-14B84BD0A5D3Q46989579-9DB33DD2-3A39-4F63-B666-2D19299BBB6CQ47251957-1074A62B-E937-4C2A-A98D-A2B3D0BB41F6Q48544109-20734F67-5782-4B58-A798-1AC7F907D318Q50504484-711248D1-80D3-432E-BF51-3F4A9B8A0043
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Timothy Mcclanahan
@ast
Timothy Mcclanahan
@en
Timothy Mcclanahan
@es
Timothy Mcclanahan
@nl
Timothy Mcclanahan
@sl
type
label
Timothy Mcclanahan
@ast
Timothy Mcclanahan
@en
Timothy Mcclanahan
@es
Timothy Mcclanahan
@nl
Timothy Mcclanahan
@sl
altLabel
Tim
@en
prefLabel
Timothy Mcclanahan
@ast
Timothy Mcclanahan
@en
Timothy Mcclanahan
@es
Timothy Mcclanahan
@nl
Timothy Mcclanahan
@sl
P106
P1153
7005454038
P2038
Tim_Mcclanahan
P21
P31
P496
0000-0001-5821-3584