about
Changes in the microbial community structure of bacteria, archaea and fungi in response to elevated CO(2) and warming in an Australian native grassland soil.Selective grazing modifies previously anticipated responses of plant community composition to elevated CO(2) in a temperate grassland.Elevated CO2 and warming effects on grassland plant mortality are determined by the timing of rainfall.Partitioning direct and indirect effects reveals the response of water-limited ecosystems to elevated CO2.Simple additive effects are rare: a quantitative review of plant biomass and soil process responses to combined manipulations of CO2 and temperature.Light as a key driver of freshwater biofouling surface roughness in an experimental hydrocanal pipe rig.Responses to mild water deficit and rewatering differ among secondary metabolites but are similar among provenances within Eucalyptus species.A water availability gradient reveals the deficit level required to affect traits in potted juvenile Eucalyptus globulus.Seasonal not annual rainfall determines grassland biomass response to carbon dioxide.Influence of warming on soil water potential controls seedling mortality in perennial but not annual species in a temperate grassland.Stability of plant defensive traits among populations in two Eucalyptus species under elevated carbon dioxide.Plant responses to CO2 are a question of time.Interactive effects of nitrogen and irradiance on sustained xanthophyll cycle engagement in Eucalyptus nitens leaves during winterFlowering phenology in a species-rich temperate grassland is sensitive to warming but not elevated CO2The response of leaf morphology to irradiance depends on altitude of origin in Nothofagus cunninghamiiCold hardening reduces photoinhibition of Eucalypts nitens and E. pauciflora at frost temperaturesGlobally consistent influences of seasonal precipitation limit grassland biomass response to elevated CO2A meta-analysis of 1,119 manipulative experiments on terrestrial carbon-cycling responses to global change
P50
Q30572160-08D2BDA9-E084-47A5-8D58-9B218FEC08B9Q30653586-C621AC60-116E-4BA8-BAA3-36175C786990Q36320288-96328FB4-AF3A-4DCE-8D64-CE6520404753Q37417775-8F640C95-4DF6-4DB4-B699-25619A8E94A3Q38185627-8A64692A-A3B0-450F-B5E0-9D1C415D6CBCQ38407654-2DDE2E11-6CCE-4F3E-AB06-81AD8C05A578Q38950341-239B127B-DC9A-49F2-B84F-87223DB1E629Q39236421-D4A60406-2987-4DCC-A274-001C413055A6Q46888543-46EF511B-5474-4063-ACE7-7E01667BFD22Q51119422-BE5EFDDB-5E03-4335-8A1D-5F430E204776Q51571758-BDE85076-E551-4E53-A5C8-1867B846A0C2Q52576508-212D63CC-4966-4DC7-A664-0B15AEF6A919Q73150368-957C59CB-CE96-465C-B215-B2D9EAF53536Q80886034-E52D69D2-2E96-4C99-83E1-3C32F0B903C4Q82258494-8C464EE0-85D3-4EE4-88F6-C20AE33F183BQ89567419-BA6B961D-D751-4587-8429-9A13A9FBC344Q91430143-9C5D0604-9D7F-4B5C-A060-BB4C427769EBQ92710327-CB488562-0D3B-4EEF-AC23-85581B728CB3
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mark J Hovenden
@ast
Mark J Hovenden
@en
Mark J Hovenden
@es
Mark J Hovenden
@nl
type
label
Mark J Hovenden
@ast
Mark J Hovenden
@en
Mark J Hovenden
@es
Mark J Hovenden
@nl
prefLabel
Mark J Hovenden
@ast
Mark J Hovenden
@en
Mark J Hovenden
@es
Mark J Hovenden
@nl
P106
P31
P496
0000-0001-7208-9700