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Data from: Sexual antagonism for resistance and tolerance to infection in Drosophila melanogaster
负责人:
关键词:
Sexual Antagonism Sexual Dimorphism Antagonistic Pleiotropy Immunity Host-Parasite Coevolution
DOI:
doi:10.5061/dryad.t7t5r
摘要:
-immunological studies assess host resistance to parasites rather than the host's ability to maintain fitness during infection (tolerance). Distinguishing bet
Data from: Effects of protein malnutrition on tolerance to helminth infection
负责人:
关键词:
intestinal permeability;Mus musculus;helminth;Heligmosomoides polygyrus;resistance;Tolerance
DOI:
doi:10.5061/dryad.r540f
摘要:
genetic variation for tolerance, but little is known about how environmental factors affect tolerance. Here, we used the intestinal nematode Heligmosomoides polygyrus
Data from: The role of the environment in the evolution of tolerance and resistance to a pathogen
负责人:
关键词:
Ecology: evolutionary;Evolution: experimental;Evolution: host\/parasite;Aedes aegypti;Coevolution;Environmental variability;Epidemiology;Vavraia culicis;Ecology: experimental
DOI:
doi:10.5061/dryad.r1s5d
摘要:
Defense against parasites can be divided into resistance, which limits parasite burden, and tolerance, which reduces pathogenesis at a give
Data from: Temporally autocorrelated environmental fluctuations inhibit the evolution of stress tolerance
负责人:
关键词:
virus;Evolution: experimental;Stochastic environments;Trade offs;Theory;Modeling: population ecology;Adaptation
DOI:
doi:10.5061/dryad.j57p9
摘要:
and anthropogenic stress. Generally speaking, selection is expected to favor adaptations that reduce the negative impact of environmental stress (i.e., stress tolerance
Data from: The combined effects of temporal autocorrelation and the costs of plasticity on the evolution of plasticity
负责人:
关键词:
development;Adaptation speed;cost of plasticity;reversible traits;strength of selection;Environmental Predictability;Tolerance
DOI:
doi:10.5061/dryad.4p30k
摘要:
. That is, the evolution of plasticity is constrained by the high cost of plasticity in combination with high tolerance for environmenta
Data from: Species’ range dynamics affect the evolution of spatial variation in plasticity under environmental change
负责人:
关键词:
climate change;Genetics: quantitative;Biogeography;Phenotypic Plasticity;Geographic ranges;Modeling: individual based;Colonization;Methods: computer simulations
DOI:
doi:10.5061/dryad.2nc0bn1
摘要:
While clines in environmental tolerance and phenotypic plasticity along a single species' range have been reported repeatedly and are of special int
Data from: Ecological novelty by hybridization: experimental evidence for increased thermal tolerance by transgressive segregation in Tigriopus
负责人:
关键词:
reproductive isolation;hybridization;Holocene;speciation;Tigriopus californicus;Adaptation
DOI:
doi:10.5061/dryad.33d5s
摘要:
for the diversification of this species: survivorship during development and tolerance to thermal stress. Experimental crosses between two population pairs show that mos
Data from: Evolution, not transgenerational plasticity, explains the adaptive divergence of acorn ant thermal tolerance across an urban-rural
负责人:
关键词:
Temnothorax curvispinosus;global change;thermal physiology;Maternal Effect;urban evolution;Holocene;Contemporary Evolution;speciation;Adaptation
DOI:
doi:10.5061/dryad.0r75421
摘要:
either maternally or paternally in the hybrid pairings as would be expected for strong parental or grandparental effects mediated through a single sex
Data from: The ontogeny of tolerance curves: habitat quality vs. acclimation in a stressful environment
负责人:
关键词:
DOI:
doi:10.5061/dryad.vb6k6
摘要:
in the brine shrimp Artemia to disentangle these different contributions to environmental tolerance, and investigate how they unfold along life. We placed individuals
Data from: Plasticity of thermal tolerance and its relationship with growth rate in juvenile mussels (Mytilus californianus)
负责人:
关键词:
Heat stress;rocky intertidal zone;developmental plasticity;temperature;Mytilus californianus;Growth;Acclimatization
DOI:
doi:10.5061/dryad.74sh7
摘要:
and protected sites retained differences in thermal tolerance after common garden treatment in summer. Both irreversible and reversible forms of plasticity

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