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35 results for “hatching success”

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zenodo40/100

Thermal regimes and hatching success related data for wild king cobra nests from the Western Himalayas, Uttarakhand, India

<p>This dataset, collected between 2009-2020, describes the thermal regimes of wild king cobra nests from the foothills of the Western Himalayas of Uttarakhand, northern India. Nest and ambient temperatures at nest sites were recorded every hour via automatic data loggers during, mostly, the latter part of incubation period (post natural nest-abandonment by female king cobras). Nest attributes (e.g. size, weight etc.) and hatching success parameters (i.e. percentage of hatched eggs and offspring size) are also provided per nest. All uploaded data have been analyzed in the paper: &quot;House warming: wild king cobra nests have thermal regimes that positively affect hatching success and hatchling size&quot; by Dolia et al. (currently under review in Journal of Thermal Biology.)</p>

opencc-by-4.0Nov 2022View details →
dryad36/100

Data from: To hatch and hatch not: Rejecting the hypothesis that heterochrony in vestibular mechanosensing explains poor escape-hatching success of Agalychnis spurrelli in snake attacks compared with its congener A. callidryas

<p>Phyllomedusid treefrogs hatch prematurely to escape egg predation, but escape success varies among species. During spontaneous hatching of <em>Agalychnis</em> <em>spurrelli</em>, snake attacks elicited 55% less escape-hatching than did attacks on less developed <em>A. callidryas</em>. <em>Agalychnis</em> <em>callidryas</em> use their vestibular system and, secondarily, their lateral line to sense physical disturbances that cue hatching. Since <em>A. spurrelli </em>develop faster, we hypothesized that heterochronic shifts in the onset timing of vestibular mechanosensory function, relative to hatching ability, might explain their lower escape response to mechanosensory cues. To test this, we compared the onset timing of hypoxia- and mechanosensory-cued hatching (MCH) and vestibular mechanosensory function in developmental series of <em>A. spurrelli</em> and <em>A. callidryas</em> embryos. Across species, most sibships began responding to each cue at the same developmental stage. MCH onset in A. spurrelli was associated with vestibular function onset, as indicated by measurements of the vestibulo-ocular reflex (VOR). Indeed, the first <em>A. spurrelli</em> embryos to show MCH had VOR amplitudes similar to those previously found for <em>A. callidryas</em> at the onset of MCH.  These results indicate that low escape-hatching success in <em>A. spurrelli</em> is not caused by a relative delay in the onset of vestibular mechanosensory function, rejecting our initial hypothesis; the developmental timing of vestibular mechanosensing and its role in predator-induced hatching appears conserved. Our observations of both higher escape success of larger clutches in snake attacks and hatching complications in flooded A. spurrelli suggest, instead, that differences in egg capsule and clutch structure may contribute to species differences in escape-hatching success.</p>

opencc-zeroDec 2023View details →
dryad36/100

Data from: Paternal hatching care regulates the timing, synchrony, and success of hatching in a coral reef fish

<p>In oviparous species, the timing of hatching is a crucial decision, but for developing embryos, assessing cues that indicate the optimal time to hatch is challenging. In species with parental care, parents can assess environmental conditions and induce their offspring to hatch. We provide the first documentation of parental hatching regulation in a coral reef fish, demonstrating that male neon gobies (<em>Elacatinus colini</em>) directly regulate hatching by removing embryos from the clutch and spitting hatchlings into the water column. All male gobies synchronized hatching within 2h of sunrise, regardless of when eggs were laid. Paternally-incubated embryos hatched later in development, more synchronously, and had higher hatching success than artificially-incubated embryos that were shaken to simulate paternal hatching cues or not stimulated. Artificially-incubated embryos displayed substantial plasticity in hatching times (range: 88 – 244 hours post-fertilization), suggesting that males could respond to environmental heterogeneity by modifying the hatching time of their offspring. Finally, paternally-incubated embryos hatched with smaller yolk sacs and larger propulsive areas than artificially-incubated embryos, suggesting that paternal effects on hatchling phenotypes may influence larval dispersal and fitness. These findings highlight the complexity of fish parental care and may have important, and currently unstudied, consequences for fish population dynamics.</p>

opencc-zeroSep 2022View details →
dryad36/100

Data from: Optimising the hatching success of artificially incubated eggs for use in a conservation program for the western saw-shelled turtle (Myuchelys bellii)

<p>Artificial incubation of eggs and the release of hatchlings into the wild is a common conservation intervention designed to augment threatened turtle populations. We investigate a range of incubation temperatures to establish an optimal temperature for maximum hatching success of western saw-shelled turtle (<em>Myuchelys</em> <em>bellii</em>) eggs. We report on the influence of incubation temperature on incubation duration and hatching success and describe two experimental incubation methods which, for the same incubation temperature, resulted in 77% and 97% hatching success, respectively. Eggs were incubated at constant temperatures (27°C, 28°C and 29°C) to determine the influence of temperature on incubation period, hatchling morphology and external residual yolk. Incubation duration was negatively correlated with incubation temperature. We report on the morphology of eggs and hatchlings and show that their dimensions are positively correlated with maternal adult size and mass. A constant incubation temperature of 27°C produced the highest hatching success and smallest external residual yolk on hatching and is therefore recommended for incubation of eggs for population reinforcement programs. Our study is the first to optimise artificial incubation procedures for <em>M</em>. <em>bellii</em> and will be a valuable resource for <em>M</em>. <em>bellii</em> and other threatened freshwater turtle conservation initiatives.</p>

opencc-zeroOct 2022View details →
dryad36/100

Developmental changes in red-eyed treefrog embryo behavior increase escape-hatching success in wasp attacks

<p>The arboreal embryos of red-eyed treefrogs (<em>Agalychnis</em> <em>callidryas</em>) hatch prematurely to escape from egg-predators, and escape success increases with age. We assessed developmental changes in the behavior and hatching performance of embryos attacked by wasps (<em>Polybia</em> <em>rejecta</em>) and their contributions to improved embryo survival. We recorded videos of 4- and 5-day-old embryos exposed to wasp attacks and determined each embryo's fate. For a stratified random sample of embryos that escaped and died, we determined the occurrence, sequence, and timing of events during wasp-embryo interactions. We constructed path diagrams of event sequences, tested for age effects on transition probabilities, and measured durations of periods between key events. Overall escape success was 38% higher in older embryos. They were more likely to hatch pre-emptively than younger ones, thus less likely to experience direct attacks, suggesting that developmental gains in mechanosensory sensitivity may increase hatching responses to indirect cues. During direct attacks, embryos were equally likely to be captured by wasps at both ages and hatching speed was similar, suggesting no relevant difference in escape-hatching performance. After a wasp ruptured their egg capsule, older embryos were more likely to exit and did so much sooner; younger embryos remained in ruptured capsules for longer and were more likely to be attacked again. This developmental change in embryo behavior indicates decreased tolerance for egg-stage risk as the chance of tadpole survival increases, suggesting that ontogenetic adaptation to changing risk trade-offs contributes strongly to the developmental increase in escape success.<span></span></p>

opencc-zeroMar 2023View details →
dryad36/100

Data from: Optimising the hatching success of artificially incubated eggs for use in a conservation program for the western saw-shelled turtle (Myuchelys bellii)

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publicOct 2022View details →
dryad36/100

Developmental changes in red-eyed treefrog embryo behavior increase escape-hatching success in wasp attacks

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publicMar 2023View details →
dryad36/100

Data from: To hatch and hatch not: Rejecting the hypothesis that heterochrony in vestibular mechanosensing explains poor escape-hatching success of Agalychnis spurrelli in snake attacks compared with its congener A. callidryas

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publicDec 2023View details →
dryad36/100

Conditional female strategies influence hatching success in a communally-nesting iguana

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publicFeb 2021View details →
dryad36/100

Data from: Paternal hatching care regulates the timing, synchrony, and success of hatching in a coral reef fish

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publicSep 2022View details →
dryad32/100

Spatiotemporal variation in hatching success and nestling sex ratios track rapid movement of a songbird hybrid zone

<p>Hybridization often occurs at the parapatric range interface between closely related species, but fitness outcomes vary: hybrid offspring exhibit diverse rates of viability and reproduction when compared to their parental species. The mobile hybrid zone between two chickadee congeners ( Poecile atricapillus x P. carolinensis ) has been well studied behaviorally and genetically but the viability of hybrids, as well as the underlying mechanisms contributing to hybrid fitness, have remained unclear. To better characterize the fitness costs of hybridization in this system, we analyzed 21 years of data from four sites, including over 1,400 breeding attempts by the two species, to show that rates of hatching success changed substantially as the zone of hybridization moved across the landscape. Admixture-associated declines in hatching success correlated with reduced proportions of heterogametic (female) offspring as predicted by Haldane's rule. Our data support an underlying mechanism implicating genetic admixture of the homogametic (male) parent as the primary determinant of offspring sex ratio, via incompatibilities on the hemizygous Z chromosome. Our long-term study is the first to directly measure changes in fitness costs as a vertebrate hybrid zone moves, and it shows that changes in these costs are a way to track the distribution of a hybrid zone across the landscape.</p>

opencc-zeroJan 2022View details →
zenodo32/100

FIG. 8 in Multi-scale Assessment of Rock Barrens Turtle Nesting Habitat: Effects of Moisture and Temperature on Hatch Success

FIG. 8. Daily rainfall (mm) during the 2018 incubation period and average 15-minute soil saturation (%) at the bottom (solid line) and top (dashed line) of turtle nests (red, n ¼ 6) and haphazard sites (gray, n ¼ 6).

opennotspecifiedJun 2021View details →
zenodo32/100

FIG. 6 in Multi-scale Assessment of Rock Barrens Turtle Nesting Habitat: Effects of Moisture and Temperature on Hatch Success

FIG. 6. Mean (6 range) daily soil temperature (8C) at the depth of the nest chamber center during the 2018 incubation season for turtle nests (n ¼ 6, red) and paired haphazard sites (n ¼ 6, light gray).

opennotspecifiedJun 2021View details →
zenodo32/100

FIG. 7 in Multi-scale Assessment of Rock Barrens Turtle Nesting Habitat: Effects of Moisture and Temperature on Hatch Success

FIG. 7. Diel soil temperature (8C) pattern for turtle nests (n ¼ 6, red line) and paired haphazard sites (n ¼ 6, gray line) measured hourly (points) at depths equivalent to the bottom (A) and top (B) of the nest chambers during the 2018 summer incubation period.

opennotspecifiedJun 2021View details →
zenodo32/100

FIG. 2 in Multi-scale Assessment of Rock Barrens Turtle Nesting Habitat: Effects of Moisture and Temperature on Hatch Success

FIG. 2. Mean (695% confidence interval) hourly soil temperature (8C) at the depth of the nest chamber top (A) and bottom (B) for turtle nests during the 2018 (n ¼ 6) and 2019 (n ¼ 6) incubation period. Nest were laid in sites with a crevice (red line, n ¼ 3), ledge (gray line, n ¼ 5), or flat (black line, n ¼ 4) bedrock morphology.

opennotspecifiedJun 2021View details →
zenodo32/100

FIG. 5 in Multi-scale Assessment of Rock Barrens Turtle Nesting Habitat: Effects of Moisture and Temperature on Hatch Success

FIG. 5. Mean (6 SE) soil saturation (%) recession curves after rainfall events for sections of the turtle nest cavities with 100% hatch success (red line, n ¼ 8) and 0% hatch success (gray line, n ¼ 9) during the 2018 and 2019 incubation periods (A). Mean (6 SE) soil saturation (%) recession curves after rainfall events for turtle nests (red line, n ¼ 6) and paired haphazard sites (gray line, n ¼ 6) during the 2018 incubation period (B).

opennotspecifiedJun 2021View details →
zenodo32/100

FIG. 3 in Multi-scale Assessment of Rock Barrens Turtle Nesting Habitat: Effects of Moisture and Temperature on Hatch Success

FIG. 3. Predicted probability (695% confidence intervals) of turtle egg hatch success (n ¼ 105) in relation to mean daily soil temperature (8C) when variance of percent soil saturation during incubation was high (standard deviation of 20% saturation, gray) compared to low (standard deviation of 10% saturation, red). Mean daily incubation temperature is shown for each turtle egg and black circles represent sample size (1–3 eggs [small circle], 4–6 eggs [medium circle], or 7þ eggs [large circle]).

opennotspecifiedJun 2021View details →
zenodo32/100

FIG. 1 in Multi-scale Assessment of Rock Barrens Turtle Nesting Habitat: Effects of Moisture and Temperature on Hatch Success

FIG. 1. In a rock barrens landscape in the eastern Georgian Bay region (A), turtles nest in shallow soil deposits underlain by bedrock which can be classified as having either a crevice (B), ledge (C), or flat (D) morphology.

opennotspecifiedJun 2021View details →
zenodo32/100

FIG. 3. A in A Successful Reintroduction of Columbia Spotted Frog (Rana luteiventris) through Repatriation of Recently Hatched Larvae

FIG. 3. A satellite image and the approximate locations of CSF egg mass deposition locations at the Taylors Fork repatriation site.

opennotspecifiedMar 2022View details →
zenodo32/100

FIG. 1 in A Successful Reintroduction of Columbia Spotted Frog (Rana luteiventris) through Repatriation of Recently Hatched Larvae

FIG. 1. Location of Taylors Fork CSF repatriation site and North Fork (CSF donor site) in the United States Uinta-Wasatch-Cache National Forest, Utah, including the location of historic CSF locations in the Weber River watershed.

opennotspecifiedMar 2022View details →

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