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zenodo32/100

FIGURE 1 in New genus and two new species of the family Ethmolaimidae (Nematoda: Chromadorida), found in two different cold-seep environments

FIGURE 1. (A) Bathymetric map of the Darwin MV with the core locations on the MV indicated (adapted from Vanneste et al. 2011) (B) Schematic representation of the sampling strategy. PUC: push core, sampled for pore-water geochemistry and meiofaunal community analyses; MC: megacorer, sampled for meiofaunal community analyses (Pape et al. 2011).

opennotspecifiedDec 2013View details →
zenodo32/100

FIGURE 3 in New genus and two new species of the family Ethmolaimidae (Nematoda: Chromadorida), found in two different cold-seep environments

FIGURE 3. Genera of the family Ethmolaimidae. Adapted from Warwick et.al. (1998), Jensen (1985, 1994). Subfamily Ethmolaiminae: A—Ethmolaimus, B—Paraethmolaimus; Subfamily Neotonchinae: C—Comesa, D— Dystomanema, E— Filitonchoides, F—Filitonchus, G—Gomphionchus, H—Gomphionema, I—Nannolaimus, J—Neotonchus.

opennotspecifiedDec 2013View details →
zenodo32/100

FIGURE 5 in New genus and two new species of the family Ethmolaimidae (Nematoda: Chromadorida), found in two different cold-seep environments

FIGURE 5. Dystomanema cadizensis gen. nov., sp. nov. Holotype Male. A: entire body; B–C: head; D: pharynx, detail ventral gland; E: supplements, spicules, caudal glands; F: supplements, detail clear patch. Paratype Male. G: upper view of supplements; H: clear patch (Scale bars: A= 200 µm; B, C, F, G, H= 20 µm; D, E= 50 µm).

opennotspecifiedDec 2013View details →
zenodo32/100

Lizard nest environments differ between suburban and forest habitats

<p>These data were analysed and presented in the the accepted manuscript to the Biological Journal of the Linnean Society titled &quot;Lizard nest environments differ between suburban and forest habitats.&quot;</p> <p>2017_miami_nest_temp.csv -- temperature of plots with nest and without nest</p> <p>2017_soil_moisture.csv -- percentage moisture of plots with and without nests.</p> <p>2017_distances.csv -- distances to tree, tree size, substrate information for plots with and without nests,</p> <p>2017_shade.csv -- percent canopy openness of plots with and without nests</p> <p>View ReadMe.txt for meta-data details.</p> <p>&nbsp;</p>

opencc-by-nc-sa-4.0Dec 2018View details →
zenodo32/100

Supplementary material 2 from: Szlavecz K, Vilisics F, Tóth Z, Hornung E (2018) Terrestrial isopods in urban environments: an overview. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 97-126. https://doi.org/10.3897/zookeys.801.29580

List of terrestrial isopod species records in urban areas : Explanation note: Species name have been cross-checked with the world catalog by Schmalfuss (2003). Synonyms have been changed to valid species names. In some cases the species was not listed in the catalog. Notes regarding uncertainties are also from Schmalfuss (2003).

opencc-zeroDec 2018View details →
zenodo32/100

Supplementary material 1 from: Szlavecz K, Vilisics F, Tóth Z, Hornung E (2018) Terrestrial isopods in urban environments: an overview. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 97-126. https://doi.org/10.3897/zookeys.801.29580

List of cities with terrestrial isopod records : Explanation note: Publications older than 70 years are not included. Localities listed here are mapped on Fig. 2 in the text. Source of geographical coordinates and population data: https://latitude.to

opencc-zeroDec 2018View details →
zenodo32/100

Hybrid Wi-Fi and BLE Fingerprinting Dataset for Multi-Floor Indoor Environments with Different Layouts

<p>A detailed description of our dataset can be found here:&nbsp;<br> Nor Hisham, A.N.; Ng, Y.H.; Tan, C.K.; Chieng David, Hybrid Wi-Fi and BLE Fingerprinting Dataset for&nbsp;Multi-Floor Indoor Environments with Different Layouts. Data 2022, to appear.</p> <p>Please cite the paper when using the dataset.</p>

opencc-by-4.0Nov 2022View details →
zenodo32/100

Structures for article: "The reactivity of pyridine in cold interstellar environments: The reaction of pyridine with the CN radical"

<p>Set of cartesian structures supporting the article: &quot;The reactivity of pyridine in cold interstellar environments: The reaction of pyridine with the CN radical&quot;</p> <p>&nbsp;</p>

opencc-by-4.0Nov 2022View details →
zenodo32/100

Figure 6 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 6. Comparison of upper dentition of Longchuansmilus with other machairodonts. A, Longchuansmilus xingyongi gen. &amp; sp. nov., HMV87001; B, Longchuansmilus xingyongi gen. &amp; sp. nov., PDYV2522; C, Paramachaerodus maximiliani, PMU-M69, Baode, northern China; D, Paramachaerodus transasiaticus, IVPP V20106, Linxia Basin, northern China; E, Megantereon cf. nihowanensis, IVPP V26878, Sabertooth Cave, Guangxi, southern China; F, Homotherium crenatidens, THP 32067, Nihewan Basin, northern China; G, Homotherium crusafonti, AMNH FM 95297, Douglas Co., North America; H, Nimravides thinobates, UCMP V34512; I, Amphimachairodus palanderi, cast, Baode, northern China; J, Smilodon fatalis, LACMHC2001-3, Rancho La Brea tar pit.

opennotspecifiedApr 2022View details →
zenodo32/100

Figure 9 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 9. Comparison of the P4 of selected machairodonts. A, Yoshi minor from Baode, AMNH F:AM China-57-L-548; B, Paramachaerodus transasiaticus from Linxia Basin, V20106, type; C, aff. Yoshi sp., RV2006023, p4, and D6. PDYV2525.1, not same individual; D, aff. Yoshi sp., PDYV2522, p4, D6. PDYV2525.1, not same individual. Not to scale.

opennotspecifiedApr 2022View details →
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Figure 5 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 5. Cranial comparison of Longchuansmilus gen. nov. and related taxa, dorsal view. A, Metailurus major from Baode, PMU M3841; B, Paramachaerodus transasiaticus from Linxia Basin, IVPP V20106; C, Longchuansmilus xingyongi gen. &amp; sp. nov., HMV87001; D, Amphimachairodus horribilis from Baode, IVPP V15642.

opennotspecifiedApr 2022View details →
zenodo32/100

Figure 1 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 1. Location of Yuanmou and selected representatives of important Late Miocene fossil localities from China.

opennotspecifiedApr 2022View details →
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Figure 8 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 8. Comparison of the P4 of selected machairodonts. A, Yoshi minor from Baode; B, Machairodontinae gen. &amp; sp. indet., PDYV2524.2; C, aff. Yoshi sp., PDYV2524.1; D, Adelphailurus kansensis, AMNH FM 38901 type cast; E, Paramachaerodus transasiaticus, V20106, type. Not to scale.

opennotspecifiedApr 2022View details →
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Figure 4 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 4. Partial cranium of YMV87001, holotype of Longchuansmilus xingyongi gen. &amp; sp. nov. A, ventral view (A1), with enlargement of the incisor (A2); B, dorsal view; C, right lateral view; D, left lateral view; E, medial view of the upper canine, showing the serrations; F, occlusal view of the P4, showing the separation groove of preparastyle and parastyle.

opennotspecifiedApr 2022View details →
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Figure 3 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 3. Fossil dentition of Felidae from Yuanmou. A, aff. Yoshi sp. PDYV2524.1, P4; B, Machairodontinae gen. &amp; sp. indet. PDYV2524.2, P4; C, Longchuansmilus xingyongi gen. &amp; sp. nov.: C1, YMV87001, P3+P4 from both sides; C2, PDYV2522.1, P3; C3, RV2006046, lower p3?; C4, RV2006049, upper canine; C5, RV2006045, upper canine; D, aff. Yoshi sp.: D1, YMV335, upper canine; D2, PDYV2522.2, upper canine; D3, PDYV2522.3, p4; D4, RV2006047, p4; D5, RV2006023, p4; D6, PDYV2525.1, m1; D7, RV2006049, m1; D8, PDYV2525.2, broken m1; E, Amphimachairodus cf. horribilis RV2006048, p4; F, Felinae gen. &amp; sp. indet.: F1, RV2006020, upper canine; F2, RV2006021, lower canine; F3, RV2006022, p4; F4, PDYV2575, m1.

opennotspecifiedApr 2022View details →
zenodo32/100

Large Andreev Bound State Zero Bias Peaks in a Weakly Dissipative Environment

<p>This repository contains the raw data and processing Python scripts corresponding to the paper &quot;Large Andreev bound state zero bias peaks in a weakly dissipative environment&quot;</p>

opencc-by-4.0Feb 2022View details →
dryad32/100

Data from: Geothermal stickleback populations prefer cool water despite multigenerational exposure to a warm environment

<p>Given the threat of climate change to biodiversity, a growing number of studies are investigating the potential for organisms to adapt to rising temperatures. Earlier work has predicted that physiological adaptation to climate change will be accompanied by a shift in temperature preferences, but empirical evidence for this is lacking. Here, we test whether exposure to different thermal environments has led to changes in preferred temperatures in the wild. Our study takes advantage of a 'natural experiment' in Iceland, where freshwater populations of threespine sticklebacks (Gasterosteus aculeatus) are found in waters warmed by geothermal activity year-round (warm habitats), adjacent to populations in ambient-temperature lakes (cold habitats). We used a shuttle-box approach to measure temperature preferences of wild-caught sticklebacks from three warm-cold population pairs. Our prediction was that fish from warm habitats would prefer higher water temperatures than those from cold habitats. We found no support for this, as fish from both warm and cold habitats had an average preferred temperature of 13oC. Thus, our results challenge the assumption that there will be a shift in ectotherm temperature preferences in response to climate change. In addition, since warm-habitat fish can persist at relatively high temperatures despite a lower temperature preference, this suggests that preferred temperature alone may be a poor indicator of a population's adaptive potential to a novel thermal environment.</p>

opencc-zeroDec 2022View details →
dryad32/100

Data from: Harsh nutritional environment has positive and negative consequences for family living in a burying beetle

<p><span>Harsh environmental conditions in form of low food availability for both offspring and parents alike can affect breeding behaviour and success. There has been evidence that food-scarce environments can induce competition between family members, and this might be intensified when parents are caring as a pair and not alone. On the other hand, it is possible that a harsh, food-poor environment could also promote cooperative behaviours within a family, leading, for example, to the higher breeding success of pairs than of single parents. We studied the influence of a harsh nutritional environment on the fitness outcome of a family living in the burying beetle <em>Nicrophorus vespilloides</em>. These beetles use vertebrate carcasses for reproduction. We manipulated food availability on two levels: before and during breeding. We then compared the effect of these manipulations in broods with either single females or biparentally breeding males and females. We show that pairs of beetles that experienced a food-poor environment before breeding consumed a higher quantity of the carcass than well-fed pairs or single females. Nevertheless, they were more successful in raising a brood with higher larval survival compared to pairs that did not experience a food shortage before breeding. We also show that food availability during breeding and social condition had independent effects on the mass of the broods raised, with lighter broods in biparental families than in uniparental ones and on smaller carcasses. Our study thus indicates that a harsh nutritional environment can increase both cooperative as well as competitive interactions between family members. Moreover, our results suggest that it can either hamper or drive the formation of a family because parents choose to restrain reproductive investment in a current brood or are encouraged to breed in a food-poor environment, depending on former experiences and their own nutritional status.</span></p>

opencc-zeroDec 2022View details →
zenodo32/100

The Effects of Aerosol on Small-Scale Cloud-Environment Mixing: Implications for Observing Inhomogeneous Mixing

<p>This is the&nbsp;simulation output of the submitted&nbsp;manuscript &quot;The Effects of Aerosol on Small-Scale Cloud-Environment Mixing: Implications for Observing Inhomogeneous Mixing&quot; to the Journal of Geophysical Research: Atmospheres.&nbsp;</p> <p>Abstract: The mixing of clouds with their environment can change the size and number of cloud droplets, two important parameters to understand the role of clouds in the climate system. Because these changes are determined by the way a cloud mixes with its environment, they have been used to characterize the mixing process. Using a highly detailed numerical cloud model coupled with a statistical turbulence model, we show that the adequate consideration of aerosol particles from which cloud droplets grow, can alter the changes of cloud droplets during mixing. This has not been considered in the past. We identify biases that need to be considered when mixing processes are analyzed.</p> <p>The raw data presented here was produced by the aforementioned model only and is completely available.</p>

opencc-by-4.0Jan 2023View details →
zenodo32/100

Aerosol impacts on storm electrification and lightning discharges under different thermodynamic environments

<p>These are&nbsp;important data supporting the conclusion of the paper are available in the main text.</p>

opencc-by-4.0Jan 2023View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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