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Fig. 3 in Disease reservoirs threaten the recently rediscovered Podocarpus Stubfoot Toad (Atelopus podocarpus)
Fig. 3. Comparison of infection burdens in Gastrotheca tadpoles between three of the six sites. The asterisks denote significant differences. The boxplot was produced in ggplot 2 (Ginestet 2011).
Fig. 1 in Disease reservoirs threaten the recently rediscovered Podocarpus Stubfoot Toad (Atelopus podocarpus)
Fig. 1. The Podocarpus Stubfoot Toad (Atelopus podocarpus) was rediscovered along a single stream in Yacuri National Park (Ecuador) in 2016, after having been presumed extinct in the years following the last previous sighting in 1994. Photo by Phil Jervis.
Fig. 1 in From XVI to XXI century: old and recent records of Brachyteles arachnoides (Primates, Atelidae) in the State of Rio de Janeiro
Fig. 1. Map of the distribution of Brachyteles sp. in Rio de Janeiro collected from records from the 16th century to the present day and with adaptations from data from Aguirre (1971).
Fig. 8. Recent crustacean Euphausia superba Dana, 1852 in Soft-part preservation in two species of the arthropod Isoxys from the middle Cambrian Burgess Shale of British Columbia, Canada
Fig. 8. Recent crustacean Euphausia superba Dana, 1852 (krill) from Gerlache Strait, Antarctica. A. Left lateral view. B. Dorsal view. C. Detail of stalked eyes after removing head shield. All light micrographs.
Fig. 1. Recent Cape hare Lepus capensis Linnaeus, 1758 RAM R2 in Head and neck posture in sauropod dinosaurs inferred from extant animals
Fig. 1. Recent Cape hare Lepus capensis Linnaeus, 1758 RAM R2 in right lateral view, illustrating maximally extended pose (A) and ONP (B): skull, cervical vertebrae 1–7 and dorsal vertebrae 1–2. Note the very weak dorsal deflection of the base of the neck in ONP, contrasting with the much stronger deflection illustrated in a live rabbit by Vidal et al. (1986: fig. 4).
Fig. 2. Recent chicken Gallus domesticus Linnaeus, 1758 RAM R1 in Head and neck posture in sauropod dinosaurs inferred from extant animals
Fig. 2. Recent chicken Gallus domesticus Linnaeus, 1758 RAM R1 in right lateral view, illustrating maximally extended pose (A) and ONP (B): last four cervical and first four dorsal vertebrae. Note the strong ventral deflection of the base of the neck in ONP, contrasting with the very strong dorsal deflection illustrated in a live chicken by Vidal et al. (1986: fig. 7).
Geodetic Monitoring of the Recent Activity and the Dome Forming Eruption at Nevado del Ruiz (Colombia), 2010-2023
<p><a name="_Hlk160011067"></a>Nevado del Ruiz volcano in Colombia is known for the catastrophic eruption of 1985 that destroyed the villages of Armero and Chinchiná. This was not its first destructive event; similar eruptions occurred in 1595 and 1845. Unfortunately, the sparse geodetic data available in 1985 did not provide a clear warning of an impending eruption. Since 1985, geodetic monitoring has evolved, incorporating tilt, GNSS and InSAR. Combined with seismic, geochemical, and geological monitoring, these techniques have enhanced the understanding of the volcano, improved hazards assessment and mitigated the risk from the eruptions of 1989, 2012, and 2015-2019, as well as the unrest over the last 11 years. Modeling of deformation data over the past 13 years reveals complex interactions between local and regional magma reservoirs. Before February 2012, the volcano deflated, initially thought to be due to gravitational collapse of the edifice, but now attributed to the depressurization of a shallow magma reservoir. This reservoir has been feeding ash emissions, gas release (2012-2023), and the dome forming eruption (2015-2019). The inflation of the volcanic edifice from 2012 to 2023 is linked to a deep pressurization source beneath the Nevado de Santa Isabel volcano, about 9 km southwest of Nevado del Ruiz.</p>
Recent Tectonic Activity in and Around the Posidonius Crater, Moon-Version 5
<p>The shapefiles and .scc files of the version 5 manuscript: "Recent tectonic activity in and around the Posidonius crater, Moon."</p>
Fig. 2 in The origin and diversification of the Entorrhizales: deep evolutionary roots but recent speciation with a phylogenetic and phenotypic split between associates of the Cyperaceae and Juncaceae
Fig. 2 Collapsed chronogram for Basidiomycota and Entorrhizomycota evolution. The tree topology represents the consensus of trees inferred with BEAST from combined 18S + 28S + rpb1 domains B-C sequences from 83 Basidiomycota species, three Entorrhizomycota species and three Ascomycota species as outgroup. Alignment length = 3903. The age estimation mean is followed by the 95% highest density probability range in square brackets. Numbers on branches represent bootstrap values obtained from 1000 replicates (values ≥ 70), maximum support of 100 is encoded with bold lines. For full dataset, see Supplementary material (Fig. S1). Abbreviations: Ordo., Ordovician; Sil., Silurian; Carbon., Carboniferous; Paleo., Paleogene; N., Neogene
Data and code for the publication: "Unexpected anthropogenic emission decreases explain recent atmospheric mercury concentration declines"
<p>A. Feinberg, Aug 2024</p> <p>arifeinberg@gmail.com</p> <p> </p> <p>Essential data and code for the publication: Feinberg et al. : Unexpected anthropogenic emission decreases are required to explain recent atmospheric mercury concentration declines</p> <p> </p> <p>The directories include:</p> <p>1) analysis<strong>_</strong>plotting<strong>_</strong>scripts/ - all analysis scripts used to analyze observations, produce input data, and plot figures for paper</p> <p>2) GC<strong>_</strong>code/ - Archived GEOS-Chem code used to simulate the runs in this paper</p> <p>3) GC<strong>_</strong>data/ - GEOS-Chem simulation data and run scripts can be found here for the following runs:</p> <p>BASE - run2021</p> <p>BASE+LEG - run2022</p> <p>DEC<strong>_</strong>LEG<strong>_</strong>ONLY - run2024</p> <p>ZHANG23 - run2025</p> <p>DEC<strong>_</strong>ANT<strong>_</strong>NH - run2026</p> <p> </p> <p>4) input<strong>_</strong>data/ - input data used to run GEOS-Chem</p> <p> </p> <p>Please refer to other README.md files within sub-directories and contact me for any questions.</p>
Fig. 6 in Biometric analysis of the teeth of fossil and Recent hexanchid sharks and its taxonomic implications
Fig. 6. Acrocone shape of lower teeth in Late Eocene (Early Lutetian) Hexanchus agassizi from south−western France. Bivariate plot constructed as in Fig. 4. Data for Recent Hexanchus species are indicated by symbols for H. nakamurai teeth but only by regression lines for H. griseus teeth. Holotypes, paratypes and figured teeth of the fossil species from the work of Ward (1979) are distinguished on the graph. Some H. microdon specimens (Paleocene − early Eocene) have been added for comparison.
Fig. 5 in Biometric analysis of the teeth of fossil and Recent hexanchid sharks and its taxonomic implications
Fig. 5. Acrocone shape of lower teeth in Recent hexanchid species. Small pictures illustrate the changes in acrocone size according to the L2/L3 values. Interrupted lines are regression curves from data for the two living Hexanchus species. For H. griseus, different symbols have been used to indicate the sex of the sharks (m, male; f, female; ind, indeterminate).
Fig. 3 in Biometric analysis of the teeth of fossil and Recent hexanchid sharks and its taxonomic implications
Fig. 3. Fossil Hexanchus sp. lower teeth from the Donzacq Formation of Saint−Géours−d'Auribat (late Ypresian/early Lutetian, south−western France). A. UMC−SG13, antero−lateral file, labial view. B. UMC−SG130, antero−lateral file, lingual view. C. UMC−SG15, lateral file, labial view. D. UMCSG14, antero−lateral file, labial view. E. UMC−SG131, lateral file, lingual view. F. UMC−SG132, antero−lateral file, lingual view. G. UMC−SG17, lateral file, labial view. H. UMC−SG133, lateral file, labial view. I. UMCSG134, broken lateral lower tooth with peculiar deep root, labial (I1) and lingual (I2) views. J. UMC−SG135, lateral file, labial view. K. UMC−SG12, symphysial file, lingual view.
Fig. 2 in Biometric analysis of the teeth of fossil and Recent hexanchid sharks and its taxonomic implications
Fig. 2. Overview of dental variations in lower teeth of living species of Hexanchus. Labial view of some lower teeth of Hexanchus griseus (A–L) and Hexanchus nakamurai (M–O). A. ♀uncertain (UMC−REC204bM),>300 cm TL; 1st left file (A), 3rd (uncertain) left file (A), and lateral left 1 2 file (A). B. ♂ (UMC−REC204M), 300 cm TL; 3rd right file (B), 1st right 3 1 file (B), symphysial file (B), and 1st left file (B). C. ♂ (UMC− 2 3 4 REC162M), 223 cm TL; 1st left file (C), 2nd right file (C), and 3rd left 1 2 file (C). D. ♂ (UMC−REC175M), 195 cm TL; 1st left file (D), 3rd left file 3 1 with enlargement on the mesial serrated cutting edge of the first cusp (D2), 4th left file (D), and 5th left file (D). E. ♀ (UMC−REC161M), 191 cm 3 4 TL; 1st left file (E) and 3rd left file (E). F. ♂ (UMC−REC611M), 1.08 cm 1 2 TL; 1st left file (F), 4th left file (F). G. ♀ (UMC−REC163M), 114 cm TL, 1 2 1st right file. H. ♀ (UMC−REC164M), 117 cm TL, 3nd left file. I. Unsexued (UMC−REC201M), 58 cm TL 2nd right file. J. Unsexued (UMCREC172M), 72 cm TL, 2nd left file. K. Unsexued (UMC−REC173M), 75 cm TL, 1st left file. L. ♂ (UMC−REC174M), 80 cm TL, 1st right file. M. ♀ uncertain (UMC−REC197M), 148 cm TL; 4th rigth file (M), 1st 1 right file with enlargement on the mesial serrated cutting edge of the first cusp (M2), symphysial file (M3). N. ♂ uncertain (UMC−REC192M), 145 cm TL; 3rd right file (N) and 1st left file (N). O. Sex undetermined 1 2 (UMC−REC196M), 1 m TL, 1st right file (O), 1st left file (O), 3rd lateral 1 2 file (O), and 4th lateral file (O). A–D and F–O are respectively at the 3 4 same magnification (vertical white bars). Abbreviation: TL, total length.
Fig. 1. A in Biometric analysis of the teeth of fossil and Recent hexanchid sharks and its taxonomic implications
Fig. 1. A. Simplified terminology of a Hexanchus lower tooth (Hexanchus griseus, 4th right file,>300 cm total length, UMC−REC204bM). B. Schematic drawing of measurements (homologuous points and intermediate distances) discussed in the text.
VEClim's initial assessment of Aedes albopictus activity and disease risk in three decades: historical (1980-1990), recent (2010-2020), and future (2090-2100).
<p><span>This is the initial release of VEClim, an early warning decision support system for climate-sensitive vector activity and vector-borne disease risk assessment, comprising an assessment of the seasonal dynamics of <em>Aedes albopictus</em>, the Asian tiger mosquito, and the associated risk of chikungunya virus transmission. This analysis compares three decades, i.e., historical (1980-1990), </span><span>recent <span>(2010-2020), and future (2090-2100), in terms of seasonal and geospatial averages. </span></span></p>
Figures 1-2. 1 in Recent records of Tongorma Kirkaldy (Heteroptera: Coreidae: Coreinae: Phyllomorphini) from Botswana and Zambia
Figures 1-2. 1. Specimen of Tongorma latreillii (Guérin-Méneville, 1839), near Serowe, Central District, Botswana, 12-XII-2012. (Photograph: Tony Benn). Scale: 2 mm. 2. Specimen belonging to Tongorma Kirkaldy, 1900, South Luangwa National Park, Muchinga Province, Zambia, 26-VI-2018. (Photograph: Stephen Wain).
Linked collectors and determiners for: Revision of the Recent Alvania scabra (Philippi, 1844) complex (Mollusca, Gastropoda Rissoidae) from the Mediterranean Sea with the description of a new species.
Natural history specimen data linked to collectors and determiners held within, "Revision of the Recent Alvania scabra (Philippi, 1844) complex (Mollusca, Gastropoda Rissoidae) from the Mediterranean Sea with the description of a new species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/559cdb43-c05a-4336-b8b5-c9dde799f2a9">https://bionomia.net/dataset/559cdb43-c05a-4336-b8b5-c9dde799f2a9</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/559cdb43-c05a-4336-b8b5-c9dde799f2a9">https://gbif.org/dataset/559cdb43-c05a-4336-b8b5-c9dde799f2a9</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Fossil and Recent molluscan types in the Auckland War Memorial Museum. Part 2: Polyplacophora and Scaphopoda.
Natural history specimen data linked to collectors and determiners held within, "Fossil and Recent molluscan types in the Auckland War Memorial Museum. Part 2: Polyplacophora and Scaphopoda". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/7938b142-b373-4e94-878d-03f545809ec4">https://bionomia.net/dataset/7938b142-b373-4e94-878d-03f545809ec4</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/7938b142-b373-4e94-878d-03f545809ec4">https://gbif.org/dataset/7938b142-b373-4e94-878d-03f545809ec4</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Recent noteworthy findings of fungus gnats from Finland and northwestern Russia (Diptera: Ditomyiidae, Keroplatidae, Bolitophilidae and Mycetophilidae).
Natural history specimen data linked to collectors and determiners held within, "Recent noteworthy findings of fungus gnats from Finland and northwestern Russia (Diptera: Ditomyiidae, Keroplatidae, Bolitophilidae and Mycetophilidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/78f68965-9110-4c4c-bae8-cff085ac6b15">https://bionomia.net/dataset/78f68965-9110-4c4c-bae8-cff085ac6b15</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/78f68965-9110-4c4c-bae8-cff085ac6b15">https://gbif.org/dataset/78f68965-9110-4c4c-bae8-cff085ac6b15</a>. Formatted as a Frictionless Data package.
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.