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143 results for “Ectotherm”
FIG. 3 in Droughts Reduce Growth Rates and Increase Vulnerability to Increasingly Frequent and Severe Drying Events in an Aquatic Ectotherm
FIG. 3. Conceptual figure depicting sex-specific consequences of drying event frequency and severity coupled with droughts. Only Greater Siren, Siren lacertina, reaching a minimum size quickly enough (within the size refuge) persist through drying events. Recruitment of newly hatched individuals into the size refuge requires consecutive years of growth uninterrupted by major drying events. Males (orange lines) grow faster than females (purple) and both grow faster under average (PDSI = 0, solid line) versus moderate drought conditions (dashed lines). Increased drying event severity (arrow) increases the lower bounds of the size refuge, and increased drying event frequency (arrow) decreases the number of sequential years available for growth and accrual of estivation potential. Only growth trajectories reaching size refuge parameter space recruit into the population. The last drying event at Dry Bay lasted 1.6 yr and was only 9 yr after the previous drying event. Growth trajectories are model projections incorporating sex and growing season PDSI.
Fig. 3 in Comparative thermoregulation of sympatric endothermic and ectothermic cicadas (Homoptera: Cicadidae: Tibicen winnemanna and Tibicen chloromerus )
Fig. 3 Distribution of T. winnemanna Tb as a function of Ta for animals classified as ''inactive'' during the evening chorus (solid line, open circles, y ˆ 12.04 + 0.620x, r ˆ 0.834) and the Tbs of T. winnemanna after the species' evening activity period (dashed line, filled circles, y ˆ 15.73+0.435x, r ˆ 0.657). Although the slope of the regression for ''inactive'' animals is significantly dierent from one (t ˆ)3.20, df ˆ 12, P ˆ 0.0038), twoanimals hadbody temperatures equal to ambient temperature. Mean Tbs and the temperature gradient of ''inactive'' animals is significantly lower than ''active'' (soundproducing) animals (see text). The slope of the linear regression after activity is not significantly dierent from one, showing that T. winnemanna becomes a thermoconformer during the night (t ˆ)1.603, df ˆ 2, P ˆ 0.1251)
Fig. 2 in Comparative thermoregulation of sympatric endothermic and ectothermic cicadas (Homoptera: Cicadidae: Tibicen winnemanna and Tibicen chloromerus )
Fig. 2 Evening Tb distribution of T. chloromerus (solid line, filled circles, y ˆ 9.47 + 0.708x, r ˆ 0.761) and body temperature as a function of Ta in T. winnemanna (dashed line, open circles, y ˆ 16.34 + 0.618x, r ˆ 0.695) producing sound (''active'' animals) during the species' normal evening activity period. The slope of the regression for T. chloromerus is not significantly dierent than one, indicating that the species is a thermoconformer during the evening (t ˆ)9.673, df ˆ 4, P ˆ 0.1941). The slope of the regression for T. winnemanna is significantly dierent than one, indicating that T. winnemanna regulates Tb without access to solar radiation (t ˆ)5.736, df ˆ 92, P 0:00001)
Fig. 1 in Comparative thermoregulation of sympatric endothermic and ectothermic cicadas (Homoptera: Cicadidae: Tibicen winnemanna and Tibicen chloromerus )
Fig. 1 Diurnal body temperature (Tb) of Tibicen chloromerus (solid line, filled circles, y ˆ 31.35 + 0.202x, r ˆ 0.217) and T. winnemanna (dashed line, open circles, y ˆ 18.70 + 0.498x, r ˆ 0.619) as a function of ambient temperature (Ta). The slope of the linear regression is significantly dierent from one, suggesting thermoregulation (t ˆ)5.739, df ˆ 21, P <0.00001) for T. chloromerus and (t ˆ)2.509, df ˆ 10, P <0.02) for T. winnemanna
Diet mediates thermal performance traits: implications for marine ectotherms
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Data from: A warmer environment can reduce sociability in an ectotherm
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Data from: Thermal landscape change as a driver of ectotherm responses to plant invasions
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Low-cost tools mitigate climate change during reproduction in an endangered marine ectotherm
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Data from: Highway to the danger zone: exposure-dependent costs of immunity in a vertebrate ectotherm
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Data from: Bergmann’s Rule rules body size in an ectotherm: heat conservation in a lizard along a 2200-meter elevational gradient
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Data from: Floral reflectance, color, and thermoregulation: what really explains geographic variation in thermal acclimation ability of ectotherms?
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Data from: Why does the rate of signal production in ectotherms vary with temperature?
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Data from: The influence of ecological and life history factors on ectothermic temperature-size responses: analysis of three Lycaenidae butterflies (Lepidoptera)
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Ectothermic omnivores increase herbivory in response to rising temperature
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Data from: Size matters: individual variation in ectotherm growth and asymptotic size
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Thermal ecology and baseline energetic requirements of a large-bodied ectotherm suggest resilience to climate change
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Data from: Tail loss and telomeres: consequences of large-scale tissue regeneration in a terrestrial ectotherm.
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Capture history data for: Sub-seasonal correlation between growth and survival in three sympatric aquatic ectotherms
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Data from: A metabolic syndrome in terrestrial ectotherms with different elevational and distribution patterns
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Data from: Integrating thermal physiology within a syndrome: locomotion, personality and habitat selection in an ectotherm
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International Brain Laboratory public data
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