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80 results for “Tigriopus”
FIGURE 17 in Two new species of Tigriopus Norman, 1869 from Chonburi Province, Thailand (Crustacea: Copepoda: Harpacticidae)
FIGURE 17. Tigriopus wannapaensis sp. nov. (♂): (A) right antennule, anterior; (B) P5, female, anterior; (C) P5, male, anterior.
FIGURE 3 in Two new species of Tigriopus Norman, 1869 from Chonburi Province, Thailand (Crustacea: Copepoda: Harpacticidae)
FIGURE 3. Tigriopus namsaiensis sp. nov. (♀): (A) rostrum, dorsal; (B) right antennule, anterior; (C) left antenna anterior.
FIGURE 7 in Two new species of Tigriopus Norman, 1869 from Chonburi Province, Thailand (Crustacea: Copepoda: Harpacticidae)
FIGURE 7. Tigriopus namsaiensis sp. nov. (♂): (A) allotype, habitus, dorsal; (B) allotype, habitus, lateral; (C) caudal ramus seta V; (D) antenna, anterior.
FIGURE 4 in Two new species of Tigriopus Norman, 1869 from Chonburi Province, Thailand (Crustacea: Copepoda: Harpacticidae)
FIGURE 4. Tigriopus namsaiensis sp. nov. (♀): (A) mandible, anterior; (B) maxillule, anterior; (C) maxilla, anterior; (D) maxilliped, anterior.
FIGURE 8 in Two new species of Tigriopus Norman, 1869 from Chonburi Province, Thailand (Crustacea: Copepoda: Harpacticidae)
FIGURE 8. Tigriopus namsaiensis sp. nov. (♂: A–B, D) (♀: C): (A) rostrum, dorsal; (B) left antennule, anterior; (C) P5, anterior; (D) P5, anterior.
Data from: Genomic scans reveal multiple mito‐nuclear incompatibilities in population crosses of the copepod Tigriopus californicus
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Data from: Hybrid breakdown weakens under thermal stress in population crosses of the copepod Tigriopus californicus.
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Data from: Fitness and morphological outcomes of many generations of hybridization in the copepod Tigriopus californicus
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Data from: Ecological novelty by hybridization: experimental evidence for increased thermal tolerance by transgressive segregation in Tigriopus californicus
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Data from: Reverse genetics in the tidepool: knockdown of target gene expression via RNA interference in the copepod Tigriopus californicus
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Data from: Phenotypic and transcriptomic responses to salinity stress across genetically and geographically divergent Tigriopus californicus populations
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Data from: Gene conversion yields novel gene combinations in paralogs of GOT1 in the copepod Tigriopus californicus
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Data from: Potential fitness tradeoffs for thermal tolerance in the intertidal copepod Tigriopus californicus
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Data from: Sex without sex chromosomes: genetic architecture of multiple loci independently segregating to determine sex ratios in the copepod Tigriopus californicus
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Data from: Postzygotic isolation involves strong mitochondrial and sex-specific effects in Tigriopus californicus, a species lacking heteromorphic sex chromosomes
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Data from: Chromosome-wide impacts on the expression of incompatibilities in hybrids of Tigriopus californicus
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Figure 5 in Influence of CO -induced seawater acidification on the development and lifetime reproduction of Tigriopus japonicus Mori, 1938
Figure 5. Average number of nauplii per viable egg sac (N = 3) at four pH levels (median indicated with a bar; quartiles, minimum and maximum also shown).
Figure 1 in Influence of CO -induced seawater acidification on the development and lifetime reproduction of Tigriopus japonicus Mori, 1938
Figure 1. Effect of carbon dioxide (CO2)-induced seawater acidification on development time [mean ± standard deviation (SD), N = 3] of Tigriopus japonicus (N–C, nauplius to copepodite; C–A, copepodite to adult).
Population growth in response to density and extrinsic heat waves in the copepod, Tigriopus californicus
<p>Heat waves are transient environmental events but can have lasting impacts on populations through lethal and sub-lethal effects on demographic vital rates. Sub-lethal temperature stress affects individual energy balance, potentially affecting individual fitness and population growth. Environmental temperature can, however, have distinct effects on different life-history traits, and the net effect of short-term temperature stress on population growth may lead to different population responses over different time frames. Furthermore, sublethal temperature responses may be density dependent, leading to potentially complicated feedbacks between heat stress and demographic responses over time. Here, we test the hypotheses that: (i) populations subjected to higher heat wave temperatures and longer heat wave durations are more negatively affected than those subjected to less intense and shorter heat waves, (ii) heat wave effects are more pronounced during density-dependent population growth phases, and (iii) population density patterns over time mirror the short-term population growth rate responses. We subjected experimental populations of the marine copepod <em>Tigriopus californicus</em> to short-term heat stress perturbations ("heat waves") at two different time points during a 100-day period. Overall, we found that population growth rates and density responded similarly (and moderately) to heat wave intensity and duration, and that the heat wave effects on populations were largely density-dependent. We detected heat wave effects on population growth and density at low densities, but not at high densities. At low densities, we found that population growth declined with heat wave duration for the more intense heat wave intensity group, but did not detect an effect of heat wave duration within the less intense heat wave intensity group. Our study demonstrates that while ephemeral density-independent factors can influence population vital rates, understanding the longer-term consequences of transient perturbations on populations requires understanding these effects in the context of density dependence and its relationship to temperature. Higher densities may buffer the negative effects of intense heat waves and confer some degree of resilience.</p>
Figure 12 in A new species of Tigriopus (Copepoda: Harpacticoida: Harpacticidae) from Thailand with a key to the species of the genus
Figure 12. Tigriopus sirindhornae sp. nov., male. (A) Right P3; (B) right P4, posterior view.
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