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Figure 1 in Rediscovery of the endangered Bolivian tiger beetle Pometon bolivianus Huber (Coleoptera: Cicindelidae) and implications for future protection
Figure 1. Pometon bolivianus. (a) Habitat, Cerrado sensu strictu with patches of bare soil, (b) Individual on soil surface.
Figure 6 in Ethogram and time-activity budget of the collared peccary (Pecari tajacu, Tayassuidae): implications for husbandry and welfare
Figure 6. Behaviours exhibited by captive-born collared peccaries grouped into the territorial and exploratory categories. a) Dorsal gland mark; b) Rub head on ground/object; c) Nose ground; d) Nose air; e) Tasting; f) Root.
Figure 4 in Ethogram and time-activity budget of the collared peccary (Pecari tajacu, Tayassuidae): implications for husbandry and welfare
Figure 4. Behaviours exhibited by captive-born collared peccaries grouped into the social affiliative category. a) Head toss; b) Mutual rub neck; c) Mutual rub; d) Weak bite; e) Roll; f) Play in mud.
Figure 3 in Ethogram and time-activity budget of the collared peccary (Pecari tajacu, Tayassuidae): implications for husbandry and welfare
Figure 3. Behaviours exhibited by the captive-born collared peccaries grouped into reproductive category. a) Chin on back; b) Chin on head; c) Nurse; d) Mount.
Figure 1 in Ethogram and time-activity budget of the collared peccary (Pecari tajacu, Tayassuidae): implications for husbandry and welfare
Figure 1. Behaviours exhibited by the captive-born collared peccaries grouped into the locomotion and inactivity categories. a) Sequence from left to right: inactive, walking, trotting and running; b) Yawning; c) Stretching, and d) Sleeping.
Figure 2 in Ethogram and time-activity budget of the collared peccary (Pecari tajacu, Tayassuidae): implications for husbandry and welfare
Figure 2. Behaviours exhibited by the captive-born collared peccaries grouped into the social aggressive category. a) Stand over; b) Agonistic squabble; c) Tooth clack; d) Kneel; e) Lift with snout.
Figure 7 in Ethogram and time-activity budget of the collared peccary (Pecari tajacu, Tayassuidae): implications for husbandry and welfare
Figure 7. Behaviours exhibited by captive-born collared peccaries grouped into the exploratory, antipredator and maintenance categories. a) Flehmen; b) Erect dorsal bristles; c) Escaping; d) Scratching; e) Grooming.
Figure 5 in Ethogram and time-activity budget of the collared peccary (Pecari tajacu, Tayassuidae): implications for husbandry and welfare
Figure 5. Behaviours exhibited by captive-born collared peccaries grouped into the social affiliative category. a) Nose; b) Nose back; c) Nose rump; d) Nose dorsal gland; e) Nose nose; f) Nose belly.
Figure 1 in A juvenile skull of Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia), and implications for cranial ontogeny, phylogeny, and taxonomy in ornithopod dinosaurs
Figure 1. Reconstruction and comparison of the skull BSPG AS I 834 with the reconstruction of an older individual (modified from Janensch, 1955). The reconstruction of the juvenile skull was carried out by the combination of the frontoparietal plate, the left postorbital, the left squamosal, a combination of the left and the head of the right quadrate, the left jugal, the braincase, the right maxilla, the left laterodorsal maxillary process, and finally the right lower jaw with the left articular. Dark grey illustrates the skull openings, light grey illustrates the inner views of, e.g. the maxilla or the frontal, and the greyish pattern on the lower jaw and the braincase illustrates sediment. A, dorsal view of the skull reconstructed by Janensch (1955). B, left lateral view of the skull reconstructed by Janensch (1955). C, dorsal view of the reconstruction of BSPG AS I 834. For the unlabelled elements see the corresponding elements in (A). D, left lateral view of the reconstruction of BSPG AS I 834. For the unlabelled elements see the corresponding elements in (B). Note, for example, the difference of the mandibular articulation between (B) and (D). Furthermore, Janensch (1955) indicated the unknown quadratojugal in (B). This is omitted here. See Material and methods for a list of the abbreviations. Scale bars: 1 cm.
Figure 8 in A juvenile skull of Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia), and implications for cranial ontogeny, phylogeny, and taxonomy in ornithopod dinosaurs
Figure 8. Diagram resulting from the multivariate allometric analysis (MAA) of five measurements of the dentary carried out by the PAST program. The allometric coefficient is marked by the broad line imbedded in the 95% intervals. The numbers of the measurements are explained in Appendix S2.
Figure 2 in A juvenile skull of Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia), and implications for cranial ontogeny, phylogeny, and taxonomy in ornithopod dinosaurs
Figure 2. Stereo pairs of the skull BSPG AS I 834 and explanatory sketches. The sketches are relatively enlarged for better resolution. Dark grey illustrates sediment, light grey illustrates inner views of, e.g. the frontals or the dentaries, and hatched areas illustrate broken or corroded surfaces. The label affixes -r and -l stand for right and left of the respective element, where the distinction of each side is difficult to see. A, left lateral view. B, outline drawing of the left lateral view. C, outline drawing of the occipital view. D, occipital view. See Material and methods for a list of the abbreviations. Scale bars: 1 cm.
Figure 6 in A juvenile skull of Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia), and implications for cranial ontogeny, phylogeny, and taxonomy in ornithopod dinosaurs
Figure 6. Comparison of associated frontal pairs of two individuals of Dysalotosaurus, presented in articulation in dorsal view. A, the smallest frontals preserved (the left frontal GPIT/RE/1595/17; the right frontal GPIT/RE/1595/15). B, large frontals of the individual dyA (the right frontal MB.R.1377; the left frontal MB.R.1378). The orbital rim (or) is marked. Scale bar: 1 cm.
Figure 4 in A juvenile skull of Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia), and implications for cranial ontogeny, phylogeny, and taxonomy in ornithopod dinosaurs
Figure 4. Computed tomography (CT) sections of the skull BSPG AS I 834. A, horizontal section at the level of the dentary tooth crowns in ventral view. B, sagittal section at about the sagittal midline in left lateral view. C, coronal section at about the middle of the anteroposterior length in anterior view. D, coronal section about 1 cm posterior to (C) in anterior view. See Material and methods for a list of the abbreviations.
Mercury isotopic compositions in fine particles and offshore surface seawater in a coastal area of East China: Implication for Hg sources and atmospheric transformations
<p>Original data:</p> <p>sheet 1: PHg concentration</p> <p>sheet2: Chemical components in PM2.5</p> <p>sheet3: PHg isotopes</p> <p>sheet4: Seawater Hg isotopes</p>
Flowering time advances since the 1970s in a sagebrush steppe community: implications for management and restoration
<p>Climate change is widely known to affect plant phenology, but little is known about how these impacts manifest in the widespread sagebrush ecosystem of the Western US which supports a number of wildlife species of concern. Shifts in plant phenology can trigger consequences for the plants themselves as well as the communities of consumers that depend upon them. We assembled historical observations of first flowering dates for 51 species collected in the 1970 and 80s in a montane sagebrush community in the Greater Yellowstone Ecosystem and compared these to contemporary phenological observations targeting the same species and locations (2016-2019). We also assembled regional climate data (average spring temperature, day of spring snowmelt, and growing degree days) and tested the relationship between first flowering time and these variables for each species. We observed the largest change in phenology in early spring flowers, which as a group bloomed on average 17 days earlier, and as much as 36 days earlier, in the contemporary data set. Mid-summer flowers bloomed on average 10 days earlier, nonnative species 15 days earlier, and berry-producing shrubs 5 days earlier, while late summer flowering plants did not shift. The greatest correlates of early spring and mid-summer flowering were average spring temperature and day of snowmelt, which was 21 days earlier, on average, in 2016-2019 relative to the 1973-1978. The shifts in flowering phenology that we observed could indicate developing asynchronies or novel synchronies of these plant resources and wildlife species of conservation concern including: Greater sage-grouse, whose nesting success is tied to availability of spring forbs; grizzly bears -- which rely heavily on berries for their fall diet; and pollinators. This underscores the importance of maintaining a diverse portfolio of native plants in terms of species composition, genetics, phenological responsiveness to climatic cues, and ecological importance to key wildlife and pollinator species. Redundancy within ecological niches may also be important considering that species roles in the community may shift as climate change affects them differently. These considerations are particularly relevant to restoration and habitat-enhancement projects in sagebrush communities across western North America.</p>
The vocal repertoire of the bearded capuchin (Cebidae: Sapajus libidinosus): implications for understanding the complexity of neotropical primate communication
<p>Vocal communication is an essential aspect of primate social behaviour. The bearded capuchin <i>Sapajus libidinosus</i> is endemic to Brazil and some studies have described specific vocalisation types for this species; however, there is still no complete description of its vocal repertoire. Thus, this study aimed to describe the vocal repertoire of a group of <i>S. libidinosus</i> living in the<i> Parque Nacional de Brasília</i> (PNB), a protected area in the Cerrado area of Central Brazil. We carried out focal samplings and recording of vocalisations of members of a <i>S. libidinosus</i> troop in different behavioural contexts. The call analyses revealed 25 different types of vocalisations, and each call presented significant structural variation. We grouped these vocalisations according to the context of the emission or acoustic structure into the following categories: contact calls (contact note, infant babbling, trill, teeth- and lip-smacking, and sirena); foraging calls (chihui, grgr, and patinado); whistle series (WS; food-associated WS, long-distance WS, and inter-group encounter WS); aggressive calls (aggressive contact note, ascending rapid staccato, cough cough, and pip); calls in response to aggression (scream, squeal, and pulsed scream), sexual display calls (chuck and raspy oestrous call), and stress-related calls (alarm call/ bark, hiccup, hip, double hip, and wah wah). <i>S. libidinosus</i> presented a very rich vocal repertoire, revealing a pattern consistent with the repertoire of other capuchin monkey species. This is the first comprehensive description of the<i> S. libidinosus</i> vocal repertoire and highlights the complexity of neotropical primate communication.</p> <p>Vocal communication is an essential aspect of primate social behaviour. The bearded capuchin <i>Sapajus libidinosus</i> is endemic to Brazil and some studies have described specific vocalisation types for this species; however, there is still no complete description of its vocal repertoire. Thus, this study aimed to describe the vocal repertoire of a group of <i>S. libidinosus</i> living in the<i> Parque Nacional de Brasília</i> (PNB), a protected area in the Cerrado area of Central Brazil. We carried out focal samplings and recording of vocalisations of members of a <i>S. libidinosus</i> troop in different behavioural contexts. The call analyses revealed 25 different types of vocalisations, and each call presented significant structural variation. We grouped these vocalisations according to the context of the emission or acoustic structure into the following categories: contact calls (contact note, infant babbling, trill, teeth- and lip-smacking, and sirena); foraging calls (chihui, grgr, and patinado); whistle series (WS; food-associated WS, long-distance WS, and inter-group encounter WS); aggressive calls (aggressive contact note, ascending rapid staccato, cough cough, and pip); calls in response to aggression (scream, squeal, and pulsed scream), sexual display calls (chuck and raspy oestrous call), and stress-related calls (alarm call/ bark, hiccup, hip, double hip, and wah wah). <i>S. libidinosus</i> presented a very rich vocal repertoire, revealing a pattern consistent with the repertoire of other capuchin monkey species. This is the first comprehensive description of the<i> S. libidinosus</i> vocal repertoire and highlights the complexity of neotropical primate communication.</p>
Data set for the paper "Temperatures and cooling rates recorded by the New Caledonia ophiolite: implications for cooling mechanisms in young forearc sequences"
<p>Data set for the paper "Temperatures and cooling rates recorded by the New Caledonia ophiolite: implications for cooling mechanisms in young forearc sequences" by Secchiari et al.</p>
Deforestation: An implication of high rates of unemployed and low-Income household members in rural communities in Kebbi, Nigeria
<p>Deforestation has been a major environmental issue in Northern Nigeria and despite several advocacy, yet such practice has continued to endure. A root course factors are unemployment and low-income among households in Northern Nigeria. As a result of low social/financial status of the household, they depend highly on cutting down trees to make fuel wood (firewood) and charcoal (gotten from burnt wood) for the source of energy for their domestic and commercial activities. This was proven by the analysis of a secondary dataset using R-Programming, sourced from the World Bank Microdata Library, a survey carried out in 2015 in Kebbi, Nigeria titled Nigeria-Feed the Future Livelihood Project 2015, Baseline Survey worldbank.org. The dataset contains 3976 households observed and 296 values were found missing which resulted to analyzing 3758 household after the missing values were omitted. Variables describing the employed members of the household, energy sources for lighting fuel and energy sources for cooking fuel for the households were extracted from the secondary dataset. Results revealed that there are over 3000 households dependent on fuel wood as an energy source. Also, results (ANOVA) revealed that annual income of the households has significant impact on cooking fuel sources (0.0104<0.05) and has a very strong significance on lighting fuel sources (0.000<0.05). The low-income rate of households was evident showing the relationship between employed members of the households with a very strong significance on annual income of the households (0.000375<0.05). This revealed that unemployed members of the households results to low-income of the households in Kebbi make them to highly depend on the use of fuel wood (firewood) and charcoal (gotten from burnt wood) on a dialy bases as a source of energy for cooking and lighting fuel. They also export and sell fuel wood and charcoal for financial gain to neighboring countries.</p>
Dataset for Overriding lithospheric strength affects continental collisional mode selection and subduction transference: Implications for Greater
<p>This .zip file is the relative dataset for the models of <strong>Overriding lithospheric strength affects continental collisional mode selection and subduction transference: Implications for Greater India-Asia convergent system.</strong></p>
FIG. 3 in Current status of the Crocodile Lizard Shinisaurus crocodilurus Ahl, 1930 in Vietnam with implications for conservation measures
FIG. 3 Population structure of Shinisaurus crocodilurus in Vietnam. (A) Frequency histogram of snoutvent length of all encountered animals; (B) Frequency of individuals with original or regenerated tails for each nature reserve, p <0.05.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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)
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.
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.
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.
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.