Thermal Physiology and Vertical Zonation of Intertidal Animals: Optima, Limits, and Costs of Living1

By G. Somero. Integrative and Comparative Biology, 2002

903 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/88b79bef5742cd3f96dd197219768ef5ffe108c0

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Citations in the corpus

Vulnerability to climate warming and acclimation capacity of tropical and temperate coastal organisms (2016, background): “These energetic costs are difficult to quantify, but qualitative assessments suggest the costs are substantial (Somero, 2002).”
Thermal tolerance ranges and climate variability: A comparison between bivalves from differing climates (2007, background): “In crabs upper thermal limits were also closer to maximum habitat temperatures at tropical sites than temperate sites (Stillman and Somero, 2000; Somero, 2002).”
The humboldt current system of northern and central chile : Oceanographic processes, ecological interactions and socioeconomic feedback (2007, background): “This higher cost of living would be associated with the cost of repairing thermal damage (heat-shock proteins, Hsp) and adapting systems through acclimatisation (Somero 2002).”
The impacts of climate change in coastal marine systems. (2006, background): “Many organisms are more stressed near their species� range boundaries (Sorte & Hofmann 2004), and the distributions of these species can be expected to shift as environmental conditions change.”
The effects of temperature on aerobic metabolism: towards a mechanistic understanding of the responses of ectotherms to a changing environment (2015, background): “Michaelis constants are also dependent on temperature, with increasing temperature generally causing an increase in the apparent km (Somero, 1995; Somero et al., 1996; Hochachka and Somero, 2002).”
The physiology of climate change: how potentials for acclimatization and genetic adaptation will determine ‘winners’ and ‘losers’ (2010, background): “These ‘apple to apple’ comparisons allow adaptive differences among species to be clearly delineated, without ambiguities arising from phylogenetic effects (Stillman and Somero, 2000; Hochachka and Somero, 2002; Somero, 2005).”
Air temperature and winter mortality: Implications for the persistence of the invasive mussel, Perna viridis in the intertidal zone of the south-eastern United States (2011, background): “The upper distributional limits of intertidal organisms are set by physical factors such as thermal and desiccation stress (Connell, 1972; Somero, 2002; Harley et al., 2006; Hawkins et al., 2008, 2009).”
Effects of thermal and osmotic stress on growth, osmoregulation and Hsp70 in sea cucumber (Apostichopus japonicus Selenka) (2008, background): “Extensive studies showed that environmental factors, e.g. temperature and salinity, could induce the expression of heat shock proteins (Hsps) in aquatic animals (Matranga et al., 2000; Basu et al., 2002; Snyder and Ross, 2004).”
Heat hardening in a tropical lizard: geographic variation explained by the predictability and variance in environmental temperatures (2016, background): “can be costly, particularly in the production and maintenance of proteins associated with heat shock (Somero 2002).”
Mitochondrial DNA: more than an evolutionary bystander (2014, background): “In these cases, the external temperature is experienced by mitochondria, and the relative fitness of different mitochondrial genotypes types may change as a result (Somero 2002).”
Ocean waves, nearshore ecology, and natural selection (2006, background): “Similarly, the physical severity and temporal variability of the nearshore habitat have led to studies of the process of physiological adaptation in wave-swept organisms (e.g., Newell 1979; Hoffman et al. 2002; Somero 2002; Stillman 2002; Tomanek 2002).”
Physiological and ecological responses of crustaceans to ocean acidification (2011, neutral): “Two species of crabs, Necora puber and Cancer magister, which are relatively poor iono-regulators, were also able to compensate haemo lymph acid–base disturbances within 24 h when exposed to CO2 at 0.10 to 0.20 kPa (Pane & Barry 2007, Spicer et al. 2007).”
Non-commercial Research and Educational Use including without Limitation Use in Instruction at Your Institution, Sending It to Specific Colleagues That You Know, and Providing a Copy to Your Institution's Administrator. All Other Uses, Reproduction and Distribution, including without Limitation Comm (2005, neutral): “From these couplings accurate relative solute geometries and information about solute conformational change can be obtained.”