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358 results for “hatching”
LBBG_JUVENILE - Juvenile lesser black-backed gulls (Larus fuscus, Laridae) and herring gulls (Larus argentatus, Laridae) hatched in Zeebrugge (Belgium)
<p><em>LBBG_JUVENILE - Juvenile lesser black-backed gulls (Larus fuscus, Laridae) and herring gulls (Larus argentatus, Laridae) hatched in Zeebrugge (Belgium)</em> is a bird tracking dataset published by the <a href="https://inbo.be">Research Institute for Nature and Forest (INBO)</a>. It contains animal tracking data collected by the LifeWatch GPS tracking network for large birds (<a href="http://lifewatch.be/en/gps-tracking-network-large-birds">http://lifewatch.be/en/gps-tracking-network-large-birds</a>) for the project/study <strong>LBBG_JUVENILE</strong>, using trackers developed by Ornitela (<a href="https://www.ornitela.com">https://www.ornitela.com</a>). The study has been operational since 2020. In total 92 individuals of lesser black-backed gull (<em>Larus fuscus</em>) and European herring gull (<em>Larus argentatus</em>) have been tagged shortly after fledging in the colony of Zeebrugge, mainly to study their habitat use and migration behaviour. Data are automatically synced with Movebank and from there periodically archived on Zenodo (see <a href="https://github.com/inbo/bird-tracking">https://github.com/inbo/bird-tracking</a>).</p> <h2>Files</h2> <p>Data in this package are exported from Movebank study <a href="https://www.movebank.org/cms/webapp?gwt_fragment=page=studies,path=study1259686571">1259686571</a>. Fields in the data follow the <a href="http://vocab.nerc.ac.uk/collection/MVB">Movebank Attribute Dictionary</a> and are described in <code>datapackage.json</code>. Files are structured as a <a href="https://specs.frictionlessdata.io/data-package/">Frictionless Data Package</a>. You can access all data in R via <code>https://zenodo.org/records/16933166/files/datapackage.json</code> using <a href="https://frictionlessdata.github.io/frictionless-r/">frictionless</a>.</p> <ul> <li><strong>datapackage.json</strong>: technical description of the data files.</li> <li><strong>LBBG_JUVENILE-reference-data.csv</strong>: reference data about the animals, tags and deployments.</li> <li><strong>LBBG_JUVENILE-gps-yyyy.csv.gz</strong>: GPS data recorded by the tags, grouped by year.</li> </ul> <h2>Acknowledgements</h2> <p>This dataset was collected using infrastructure provided by INBO and funded by Research Foundation - Flanders (FWO) as part of the Belgian contribution to LifeWatch.</p>
Dataset for "Olfactory system structure and function in newly hatched and adult locusts"
<p>This directory contains data for the article "Olfactory System Structure and Function in Newly Hatched and Adult Locusts" by Sun, Kui, Subhasis Ray, Nitin Gupta, Zane N. Aldworth, and Mark A. Stopfer. 2023.</p><p>- The folders with extension .zarr can be read with xarray package as Datasets.</p><p>- The files with extension .mat are matlab data files.</p>
Data for "Hatching phenology is lagging behind an advancing snowmelt pattern in a high-alpine bird"
<p><strong>Abstract</strong></p> <p>To track peaks in resource abundance, temperate-zone animals use predictive environmental cues to rear their offspring when conditions are most favourable. However, climate change threatens the reliability of such cues when an animal and its resource respond differently to a changing environment. This is especially problematic in alpine environments, where climate warming exceeds the Holarctic trend and may thus lead to rapid asynchrony between peaks in resource abundance and periods of increased resource requirements such as reproductive period of high-alpine specialists. We therefore investigated interannual variation and long-term trends in the breeding phenology of a high-alpine specialist, the white-winged snowfinch, <em>Montifringilla nivalis</em>, using a 20-year dataset from Switzerland. We found that two thirds of broods hatched during snowmelt. Hatching dates positively correlated with April and May precipitation, but changes in mean hatching dates did not coincide with earlier snowmelt in recent years. Our results offer a potential explanation for recently observed population declines already recognisable at lower elevations. We discuss non-adaptive phenotypic plasticity as potential causes for the asynchrony between changes in snowmelt and hatching dates of snowfinches, but the underlying causes are subject to further research.</p>
Data underlying the publication: "Effects of hatching system on chick quality, welfare and health of young breeder flock offspring"
<p>The aim of the current study was to evaluate effects of two alternative hatching systems (hatchery-feeding and on-farm hatching)<br> compared to conventional hatching systems with respect to chick quality, welfare and health of a young breeder flock.<br> To study the effect of treatments on the competence of the humoral immune response, blood titres after a live attenuated NCD<br> vaccination was assessed.<br> To study differences in disease resilience, the susceptibility to develop tracheal inflammation after infection with a<br> life attenuated infectious bronchitis vaccine virus was assessed by trachea lesion scoring and expression of genes related<br> to epithelial integrity and inflammatory responses.</p>
Dataset: Green light during incubation: effects on hatching characteristics in brown and white laying hens
<p>Dataset used for the paper "Green light during incubation: effects on hatching characteristics in brown and white laying hens".<br> <br> Abstract:</p> <p>Providing light during incubation is being investigated as a method to improve welfare in later life in poultry. This incubation method would more closely approximate chicken natural environment compared to the current incubation in darkness. Previous studies showed promising results of light during incubation on broiler welfare, but little is known about effects of light during incubation on laying hens. Especially, information about its effects on hatching characteristics (hatch time, hatchability, chick quality, body weight and embryonic age of death) is scarce and requires investigation in both white and brown egg layers. In the current study, Dekalb White (DW) and ISA Brown (ISA) eggs were incubated in complete darkness (dark) or in a light:dark cycle of 12L:12D throughout incubation (light), resulting in four treatment groups: DW-dark, DW-light, ISA-dark, and ISA-light. In the light treatments, green LEDs of 520nm wavelength were used, at an intensity of 400 lux. First, light transmission through the eggshell was measured through 27 eggs. Then, an analysis of the effects of light during incubation on hatching characteristics was performed on 711 chicks in two consecutive experimental rounds. Light transmission was higher through white eggshells than through brown eggshells (N = 27, p < 0.001). Light during incubation had no effects on hatching characteristics (N = 711, p ≥ 0.1). Despite the difference of light transmission through eggshell between hybrids, there was no interaction between incubation treatment and hybrid on hatching characteristics (N = 471, p ≥ 0.06). Hatch time was longer and navel quality was better in DW than in ISA, while body weight and embryonic age of death were lower in DW than in ISA (all p < 0.001). Males and females had similar chick quality scores except for the beak quality, which was better for males (N = 486, p = 0.003). To conclude, green light during incubation did not negatively affect hatching characteristics in either DW nor ISA laying hen hybrids. Future research should therefore focus on its potential benefits for laying hen welfare.</p>
Fig. 95. Leiodes irregularis Hatch, 1929. A in Review of the tribes Sogdini and Leiodini from Japan and North Chishima Islands. Part II. Genera Hydnobius and Leiodes (Coleoptera: Leiodidae)
Fig. 95. Leiodes irregularis Hatch, 1929. A – aedeagus, dorsal view; B – ditto, lateral view; C – inner sac, dorsal view; D – male abdominal sternite 8; E – female abdominal sternite 8; F – coxite and stylus. Scale I: 0.5 mm for A and B; II: 0.1 mm for C; III: 0.2 mm for D and E; IV: 0.1 mm for F.
Historical Adoption of Technologies (HATCH) Dataset
<h4>About the Dataset </h4><p>The Historical Adoption of TeCHnologies (HATCH) dataset provides yearly data of technology adoption levels at both the global and country levels. The dataset includes a heterogeneous set of technologies that differ in their size, use, and spatial diffusion. The following files are available.</p><h4>Citation</h4><p>The paper can be cited as: Nemet, G., Greene, J., Müller-Hansen, F. <i>et al.</i> Dataset on the adoption of historical technologies informs the scale-up of emerging carbon dioxide removal measures. <i>Commun Earth Environ</i> <strong>4</strong>, 397 (2023). https://doi.org/10.1038/s43247-023-01056-1 </p><p><a href="https://www.nature.com/articles/s43247-023-01056-1"><strong>Paper describing the data is available here: </strong>https://www.nature.com/articles/s43247-023-01056-1</a></p><p> </p><h4>File Descriptions</h4><p><strong>HATCH1.0.csv</strong></p><p><i>Description: </i>Dataset used in the analysis for "Dataset on the adoption of historical technologies informs the scale-up of emerging carbon dioxide removal measures," which includes a limited number of country-level datapoints.</p><p> </p><p><strong>HATCH_v1.5_Clean.csv</strong></p><p> </p><p><i>Description: </i>Expanded dataset that includes country-level adoption of many technologies used in v1.0, with the addition of more global technology time series.</p><p> </p><p><strong>Tech_Growth_V1.5_variabledescriptions_Clean.yaml</strong></p><p><i>Description: </i>Description of each technology, including description, metric, and technology category.</p><p> </p><p><strong>HATCH_v1.5_DataSources.csv</strong></p><p><i>Description: </i>Lists the data sources and corresponding citations for each technology in the HATCH dataset.</p><p> </p><p>Code for calculating growth rates available at:<a href="https://zenodo.org/records/8327347 "> DOI: <strong>10.5281/zenodo.8327347</strong></a></p><p> </p><p>Table of growth rate calculations for each technology available at:<a href="https://zenodo.org/records/8327347"> </a><a href="https://zenodo.org/records/10056128">https://zenodo.org/records/10056128</a></p><p> </p><p><strong>Link to Scenario Explorer hosted by IIASA: </strong><a href="https://cdr.apps.ece.iiasa.ac.at/story/hatch/">https://cdr.apps.ece.iiasa.ac.at/story/hatch/</a></p><p> </p>
Data from: Hatching plasticity is associated with a more advanced stage at hatching in an Ambystoma with terrestrial eggs
<p>These data are from a 2019 study of embryonic development in marbled salamander (<em>Ambystoma opacum</em>) and ringed salamander (<em>Ambystoma annulatum</em>). Egg masses were collected in Arkansas in the fall of 2019 and transported to the University of North Carolina Asheville. Clutches were split and embryos were reared in one of two environments mimicking the terrestrial environment typical of <em>A. opacum</em> nests and the aquatic environment typical of <em>A. annulatum</em> egg masses. Response variables recorded include number of embryos that hatched, age (days) at hatching, Harrison stage at hatching, and dry mass at hatching.</p>
Operating diagram of hatching module, this module consists of two clearly separated sections, each consisting of two long tanks (2 × 0.2 × 0.2 m) designed to accommodate hatching boxes, a filtration tank and an independent water circulation pump with a cooling unit and UV sterilizer. This allows simultaneous monitoring of 16 batches of eggs. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of hatching module, this module consists of two clearly separated sections, each consisting of two long tanks (2 × 0.2 × 0.2 m) designed to accommodate hatching boxes, a filtration tank and an independent water circulation pump with a cooling unit and UV sterilizer. This allows simultaneous monitoring of 16 batches of eggs.
Operating diagram of larvae hatching module, this installation was used to determine the optimum larvae load during the rearing process and provided additional space for rearing several thousand larvae. It consists of nine 20-litre tanks with a glass panel along the front. They are fitted with an inlet supplying filtrated water at a rate of 100 l/h and an individual air inlet. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of larvae hatching module, this installation was used to determine the optimum larvae load during the rearing process and provided additional space for rearing several thousand larvae. It consists of nine 20-litre tanks with a glass panel along the front. They are fitted with an inlet supplying filtrated water at a rate of 100 l/h and an individual air inlet.
Operating diagram of hatching module in Zoug jars, this system consists of a 300-litre temperature-controlled isothermal enclosure containing 10 one-litre Zoug jars, each able to accommodate several hundred eggs. An ascending current holds the eggs in suspension and carries the larvae to the surface. Another bottle connected to this device collects the larvae. The water circulating in the jars is independent of that used in the filtration circuit. A cooling unit and UV sterilizer complete the installation. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of hatching module in Zoug jars, this system consists of a 300-litre temperature-controlled isothermal enclosure containing 10 one-litre Zoug jars, each able to accommodate several hundred eggs. An ascending current holds the eggs in suspension and carries the larvae to the surface. Another bottle connected to this device collects the larvae. The water circulating in the jars is independent of that used in the filtration circuit. A cooling unit and UV sterilizer complete the installation.
Operating diagram of the incubator, two tiered modules contain six independent incubators. Three shallow hatching are (220 × 60 × 17 cm) stacked on top of each other to create a compact assembly in which each tier functions independently. Eighteen trays covered with eggs can be placed in each tier, allowing the simultaneous incubation of seven to nine lays. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of the incubator, two tiered modules contain six independent incubators. Three shallow hatching are (220 × 60 × 17 cm) stacked on top of each other to create a compact assembly in which each tier functions independently. Eighteen trays covered with eggs can be placed in each tier, allowing the simultaneous incubation of seven to nine lays.
Figure 4 in Effects of temperature and duration of storage on the hatching behaviour of Heterodera latipons (Nematoda: Heteroderidae)
Figure 4. Effect of storage temperature at 20 °C, for 8 prior incubations at 10 and 15 °C for 12 weeks, on the cumulative hatching of H. latipons populations. Cumulative percentages of hatched populations. Vertical bars indicate the standard deviation of the means.
Figure 3 in Effects of temperature and duration of storage on the hatching behaviour of Heterodera latipons (Nematoda: Heteroderidae)
Figure 3. Effect of storage temperature at 5 °C, for 8 prior incubations at 10 and 15 °C for 12 weeks, on the cumulative hatching of H. latipons populations. Cumulative percentages of hatched populations. Vertical bars indicate the standard deviation of the means.
Figure 2 in Effects of temperature and duration of storage on the hatching behaviour of Heterodera latipons (Nematoda: Heteroderidae)
Figure 2. Effect of various temperatures on the emergence of J2s (J2s) of H. latiponspopulations. Cumulative percentages of hatched J2s followed by the same letter were not significantly different according to the Tukey HSD test at P ≤ 0.05. Vertical bars indicate standard deviation of the means.
Figure 1 in Effects of temperature and duration of storage on the hatching behaviour of Heterodera latipons (Nematoda: Heteroderidae)
Figure 1. Neighbour-joining tree constructed based on the ITS sequence alignment of the H. latipons populations from this study and corresponding populations representing species from GenBank. Numbers on the branches represent bootstrap values obtained from 1000 bootstrap replications.
Sublethal exposure to deltamethrin stimulates reproduction and has limited effects on post-hatching maternal care in the European earwig
<p>Data set and associated R script used to obtain the statistical results presented in the corresponding study.</p>
Evolution of a mosquito's hatching behavior to match its human-provided habitat
<p>A subspecies of the yellow fever mosquito, <em>Aedes aegypti</em>, has recently evolved to specialize in biting and living alongside humans. It prefers human odor and breeds in human-provided artificial containers rather than the forest tree holes of its ancestors. Here, we report one way this human specialist has adapted to the distinct ecology of human environments. While eggs of the ancestral subspecies rarely hatch in pure water, those of the derived human-specialist do so readily. We trace this novel behavior to a shift in how eggs respond to dissolved oxygen, low levels of which may signal food abundance. Moreover, we show that while tree holes are consistently low in dissolved oxygen, artificial containers often have much higher levels. There is thus a concordance between the hatching behavior of each subspecies and the aquatic habitat it uses in the wild. We find this behavioral variation is heritable, with both maternal and zygotic effects. The zygotic effect depends on dissolved oxygen concentration (i.e., GxE), pointing to potential changes in oxygen-sensitive circuits. Together, our results suggest that a shift in hatching response contributed to the pernicious success of this human-specialist mosquito and illustrate how animals may rapidly adapt to human-driven changes in the environment.</p>
Data for: Selection on the joint action of pairs leads to divergent adaptation and coadaptation of care-giving parents during pre-hatching care
<p>The joint actions of animals in partnerships or social groups evolve under both natural selection, from the wider environment, and social selection, imposed by other members of the pair or group. We used experimental evolution to investigate how jointly expressed actions evolve upon exposure to a new environmental challenge. Our work focused on the evolution of carrion nest preparation by pairs of burying beetles <em>Nicrophorus vespilloides</em>, a joint activity undertaken by the pair but typically led by the male. In previous work, we found that carrion nest preparation evolved to be faster in experimental populations without post-hatching care (No Care lines) than with post-hatching care (Full Care lines). Here we investigate how this joint activity evolved. After 15 generations of experimental evolution, we created heterotypic pairs (No Care females with Full Care males, and No Care males with Full Care females) and compared their carrion nest making with homotypic No Care and Full Care pairs. We found that pairs with No Care males prepared the nest more rapidly than pairs with Full Care males, regardless of the female's line of origin. We discuss how social coadaptations within pairs or groups could act as a post-mating barrier to gene flow.</p>
Fig. 5 in Effects of large temperature fluctuations on hatching and subsequent development of the diamondback moth (Lepidoptera: Plutellidae)
Fig. 5. Pupa and adult traits (mean ± SE) afer different treatments. (A) Development time of pupae, (B) emergence rate, (C) adult longevity and (D) fecundity in the diamondback moth following emergence from eggs exposed to different fluctuating temperature ranges (25 ± 0, 25 ± 2, 25 ± 4, 25 ± 6, 25 ± 8 and 25 ± 10 °C). Different letters at the tops of columns indicate significant differences at P = 0.05.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
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