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Figure 1 in Seasonality and bait type driving the diversity of dung beetle (Scarabaeidae: Scarabaeinae) communities in urban remnants of the Atlantic Forest
Figure 1. Partial map of the state of Pernambuco, with emphasis on the remnants of the Atlantic Forest (Green) and the urban area (Pink) located on the outskirts of FURB Jaguarana in the municipality of Paulista and APA Aldeia-Beberibe in the municipality of Camaragibe, PE, Brazil.
Figure 3 in Seasonality and bait type driving the diversity of dung beetle (Scarabaeidae: Scarabaeinae) communities in urban remnants of the Atlantic Forest
Figure 3. Canonical Correspondence Analysis (CCA) with group formations related to separation and types of baits used in the collection of dung beetles at FURB Jaguarana (A) and APA Aldeia-Beberibe (B).
Figure 2 in Seasonality and bait type driving the diversity of dung beetle (Scarabaeidae: Scarabaeinae) communities in urban remnants of the Atlantic Forest
Figure 2. Differences between diversity index values (q0, q1, q2) for different types of baits (feces, carrion, millipedes) in the rainy and dry season at FURB Jaguarana (A) and APA Aldeia-Beberibe (B). Meaningfulness: <0.001'***'; <0.01'**'; <0.05'*'.
CESM2.2-8P4Z data supporting Yu et al. (2024): Simulating ecosystem dynamics and marine biogeochemical cycles with multiple plankton functional types
<p><span>This dataset contains the model output from CESM2.2-8P4Z, used in Yu et al. (2024) and</span><span> </span><span>submitted to</span><span> the Journal of Advances in Modeling Earth Systems (JAMES). These are the last 20-year averaged output files from 310 years of the model simulations, which are analyzed in Yu et al., (2024). CESM2.2-8P4Z contains twelve plankton groups, including eight types of phytoplankton:</span><span> </span><span>1</span><span>) picophytoplankton groups: <em>Prochlorococcus</em>, <em>Synechococcus</em>, picoeukaryotes and diazotrophs; 2) nanophytoplankton groups:</span><span> </span><em><span><em>P</em></span></em><em><span><em>haeocystis</em></span></em><span>, <em>coccolithophores</em></span><span> </span><span>and a generic other nanophytoplankton; 3) micro-sized phytoplankton: diatoms</span><span>; and four types of zooplankton:</span><span> </span><span>small microzooplankton (5-20 u</span><span>m, such as ciliates, nanoflagellates), large microzooplankton (20-200 u</span><span>m, such as copepod nauplii, small dinoflagellates etc.), mesozooplankton (200-2000 u</span><span>m, such as smaller copepod, large dinoflagellates) and macrozooplankton (>2000 u</span><span>m, such as larger copepod, krill).</span><span> </span><span>The MARBL-8P4Z model improves seasonal simulation of the spring bloom compared with more simplified MARBL configurations, benefiting from dampened diatom blooms at higher latitudes due to a combination of bottom-up and top-down drivers.</span></p>
FIG. 3 in Boa latotecta Hermann, 1804, a junior subjective synonym of Bungarus caeruleus (Schneider, 1801) (Serpentes, Elapidae), with comments on the types of the latter taxon
FIG. 3. — Handwritten notes on Boa latotecta Hermann, 1804 by F. L. Hammer. Several notes were added at a later time by subsequent curators.
FIG. 1 in Boa latotecta Hermann, 1804, a junior subjective synonym of Bungarus caeruleus (Schneider, 1801) (Serpentes, Elapidae), with comments on the types of the latter taxon
FIG. 1. — Russell's (1796) illustration of the "Gedi Paragoodoo"; the specimen depicted is one of the syntypes of Pseudoboa caerulea Schneider, 1801.
Fig. 3 in Diversity of tissues in acanthodians with Nostolepis-type histological structure
Fig. 3. Third type of Nostolepis histological structure, with some scales formed entirely of a simple odontocytic mesodentine (A–C) and others an almost acellular, syncitial mesodentine (D). Vertical longitudinal sections. A. Nostolepis timanica (Valiukevičius 2003a: fig. 26A); LIGG, thin section 3375. B, C. Nostolepis platycrista (Valiukevičius 2003b: fig. 14B, C); LIGG, thin sections 3579 and 3582. D. Nostolepis paravolborthi (Valiukevičius 2003b: fig. 19D); LIGG, thin section 3556. Crown mesodentine slightly odontocytic in the lower crown only (the neck area). Scale bars 0.1 mm.
Fig. 2 in Diversity of tissues in acanthodians with Nostolepis-type histological structure
Fig. 2. Second type of Nostolepis histological structure, with maximum stranggewebe extent, exemplified by Vesperalia perplexa (Valiukevičius 2004: fig. 3A, B). A. LIGG, thin section 3678. A1. Vertical longitudinal section of scale showing long and dense stranglakunae with short processes and interspersed osteocyte cavities, with no simple mesodentine. A2. Wide ascending and radial vascular canals. B. LIGG, thin section 3679. B1. Scale in vertical transverse section; orientation of stranglakunae and superficial dentine tubules in an odontocytic mesodentine, and a dense concentration of osteocyte cavities in the apex of base cone (B2); stranglakunae and the vascular system of the right crown part (B3). Stoniškiai−1 borehole, Lithuania, Pridoli, Silurian. Scale bars 0.1 mm.
Fig. 1 in Diversity of tissues in acanthodians with Nostolepis-type histological structure
Fig. 1. First type of Nostolepis histological structure, with stranggewebe (posterior crown part), simple odontocytic mesodentine network (anterior crown part) and cellular bone (base). A, B, D. Nostolepis striata Pander, 1856 in vertical longitudinal sections. A. All types of tissues and ascending vascular canals (Ørvig 1967: text−fig. 5A); SMNH, thin section S 1044. B. Posterior part of crown with stranglakunae layer covered by a layer of odontocytic mesodentine (Gross 1971: fig. 2G); MNB, thin section 3658. D. Posterior part of scale containing a system of principal wide vascular canals, and a superficial layer of syncitial mesodentine (Gross 1971: fig. 6A); MNB, thin section 3935. C. Nostolepis terraborea (Valiukevičius 2003b: fig. 15C); LIGG, thin section 3644. Simple odontocytic mesodentine network and long stranglakunae in a scale without principal vascular canals. Scale bars 0.1 mm.
Fig. 6 in Diversity of tissues in acanthodians with Nostolepis-type histological structure
Fig. 6. Microstructure of scales of the sixth type of histological structure (not belonging to the Nostolepis−type). A. Nostolepis longipostera (from Valiukevičius 2003b: fig. 12A); LIGG, thin section 3594. B. Nostolepis minilonga (from Valiukevičius 2003b: fig. 17A); LIGG, thin section 3610. Multi−branched ascending vascular canals and network of non−lacunal dentinal tubules in crowns formed of a syncitial dentine with durodentine; bone in the scale bases contains only a few osteocyte cavities. C. Watsonacanthus costatus (from Valiukevičius 2003a: fig. 32B); LIGG, thin section 3302. Ascending vascular canals and the canaliculi network is slightly similar to mesodentine in the anterior crown part, and dentine−like in the posterior part, with one principal ascending branch per growth zone, and only a few interconnecting tubuli, mostly oriented upwards; cellular bone in base. Scale bars 0.1 mm.
Fig. 5 in Diversity of tissues in acanthodians with Nostolepis-type histological structure
Fig. 5. Fifth type of Nostolepis histological structure, with cellular unipolar mesodentine in crowns and cellular bone in scale bases showing the first and second order growth lines. A. Fecundosquama basiglobosa (Valiukevičius 2004: fig. 5A, B); LIGG, thin section 3683. Thin−lamellar deep base and low crown both of superpositional growth (A1) and rounded osteocyte cells in crowns without processe connections and unipolar outwardly emanated dentinal tubules (A2). B. Tchunacanthus obruchevi (Karatajūtė−Talimaa and Smith 2003: fig. 18B); LIGG, thin section 1333. The short unipolar dentinal tubules in a scale crown with areal growth zones and a base which continued growing after crown growth stopped. Outcrop 135, Tchuna River, southern Siberia, upper Llandovery, Silurian. Scale bars 0.1 mm.
Fig. 4 in Diversity of tissues in acanthodians with Nostolepis-type histological structure
Fig. 4. Fourth type of Nostolepis histological structure, with crowns composed of a bone−like cellular mesodentine, or possibly cellular bone similar to that in scale bases. Vertical longitudinal sections. A. Acritolepis urvantsevi (Valiukevičius 2003a: fig. 16F); a bone−like mesodentine developed in the lower neck and crown areas not occupied by the stranggewebe; LIGG, thin section 3350. B. Nostolepis adzvensis (Valiukevičius 2003b: fig. 7A); LIGG, thin section 3635. C. Monospina erecta (Valiukevičius 2003b: fig. 22A, B); LIGG, thin section 3535. C1. Crown tissues without vascular canals; osteocyte cavities connected to each other by short processes; crown tissue most similar to base bone. C2. The magnified area of the anterior crown part (right corner of C1). Scale bars 0.1 mm.
Fig. 5 in The type species of Cyrtosymbole and the oldest (Famennian) cyrtosymboline trilobites
Fig. 5. Scatter plot of maximum length versus maximum width of the glabella (glabellar lobe + occipital lobe) for 105 undistorted individuals. The lectotype is marked with a black triangle.
Fig. 1. A in The type species of Cyrtosymbole and the oldest (Famennian) cyrtosymboline trilobites
Fig. 1. A. Location of Cabrières village in the southeastern Montagne Noire, southern France; shaded areas indicate outcropping pre−Mesozoic massifs. B. Cyrtosymbole escoti bearing localities (La Tourière, La Serre and Peret) in the vicinity of Cabrières village; shaded areas indicate Devonian outcrops; solid lines indicate roads.
Fig. 6 in The type species of Cyrtosymbole and the oldest (Famennian) cyrtosymboline trilobites
Fig. 6. Scatter plot of maximum sagittal length versus maximum width of the pygidium (excluding articulating half−ring) for 81 undistorted individuals.
Figure 31. - Alveolar ornamentation type. A in Guide for the identification of archaeological sea sturgeon (Acipenser sturio and A. oxyrinchus) remains
Figure 31. - Alveolar ornamentation type. A: Alveolar pattern with tubercular characteristics at the edge in A. oxyrinchus (NRM 60821, 4th dorsal scute, 99 cm TL); B: Alveolar pattern in a large A. oxyrinchus (MHNNZ 19558, 6th left lateral scute, 276 cm TL); C: Lacrimale-suborbitale from Trigla lucerna (RBINS 23663; 47.5 cm SL). Note the alveolar-like ornamentation. Scale bars = 1 cm.
Fig. 5. Type I in An enigmatic chondrichthyan with Paleozoic affinities from the Lower Triassic of western Canada
Fig. 5. Type I−denticles of Listracanthus pectenatus sp. nov., Lower Triassic, Wapiti Lake, British Columbia, showing in situ arrangement (A) and aberrant morphology (B). A. As preserved in specimen TMP 95.114.52. B. Aberrant denticle as preserved in specimen TMP 2001.18.01. B1. General view. B2. Close−up of the mid−portion.
Molecular insights into substrate translocation in an elevator-type metal transporter
<p>This dataset contains biased simulation trajectories for the paper entitled "Molecular insights into substrate translocation in an elevator-type metal transporter." The trajectories are named based on the information provided in the paper. The deposited trajectories contain only the protein and zinc metal ions; due to size constraints, we retained only these components and removed the rest. The entire systems and additional input files are available upon request to the authors. The dataset comprises four folders named as follows: </p> <p>First_scenario, Second_scenario, Third_scenario, and Last_scenario.</p> <p>To extract the contents of the compressed file (.tar.gz), use the following command line:</p> <p>tar -xzvf zip_transporter.tar.gz</p> <p>Each folder contains topology files and their corresponding trajectory files. The term "Rep" in the file names denotes the simulation replicates. For instance, "rep1" indicates the first simulation replicate mentioned in the paper. All analyses were performed using cpptraj and VMD software. Custom codes for performing the analyses are available at https://gitlab.msu.edu/jafarima/zip-transporter.git.</p>
Figure 1 in Redescription of the type specimen of Chironomus oppositus Skuse, 1856
Figure 1. Male terminalia of C. oppositus type specimen. General view (left), superior volsella (right).
Figure 22 in The fauna and chronostratigraphy of the middle Miocene Mascall type area, John Day Basin, Oregon, USA
Figure 22. Parablastomeryx sp. A. Left m1 in occlusal view, JODA 2255. B. Left M1 or M2, JODA 17389. C. p4, JODA 17437. Scale bar=1mm.
ScienceDex guides
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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.