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Fig. 3 in Unveiling the morphology of the Oriental rare monotypic ant genus Opamyrma YAMANE, BUI & EGUCHI, 2008 (Hymenoptera: Formicidae: Leptanillinae) and its evolutionary implications, with first descriptions of the male, larva, tentorium, and sting apparatus
Fig. 3: Maxillolabial complex of Opamyrma hungvuong worker, nontype (AKY05vii17-06, China, Guangxi). (A) Scanning electron microscope image of maxillolabial complex in ventral view, labrum removed; (B) right maxilla in outer view; (C) labium in lateral view; (D) labium in dorsal view. Abbreviations: Ams = anteromedian sclerite; Gcss = galeal crown's stout seta; Hyp = hypopharynx; Lbp = labial palp; Lcn = lacinia; Mxco = maxillary comb; Mxp = maxillary palp; Mxst = maxillary stipes; Prm = prementum; Sglb = subglossal brush.
Fig. 7 in Unveiling the morphology of the Oriental rare monotypic ant genus Opamyrma YAMANE, BUI & EGUCHI, 2008 (Hymenoptera: Formicidae: Leptanillinae) and its evolutionary implications, with first descriptions of the male, larva, tentorium, and sting apparatus
Fig. 7: Scanning electron microscope images of legs of Opamyrma hungvuong worker, nontype (AKY05vii17-06, China, Guangxi). (A) strigil of right proleg in anterior view; (B) calcar of strigil of right proleg in anterior view; (C) strigil of right proleg in posterior view; (D) distitarsus of right proleg in posterior view; (E) tibial spurs and basitarsus of right mesoleg in anterior view; (F) tibial spurs and basitarsus of right metaleg in posterior view; (G) pretarsal claws of right metaleg in posteroventral view; (H) tibial spurs of left metaleg in anterior view. Abbreviations: Ats = anterior spur; Ca = calcar; Pts = posterior spur; Ptb = protibia; Pbts = probasitarsus; Ptss = protibial stout seta; Mnb = manubrium; Mstb = mesotibia; Msbts = mesobasitarsus; Mttb = metatibia; Mtbts = metabasitarsus.
Fig. 12 in Unveiling the morphology of the Oriental rare monotypic ant genus Opamyrma YAMANE, BUI & EGUCHI, 2008 (Hymenoptera: Formicidae: Leptanillinae) and its evolutionary implications, with first descriptions of the male, larva, tentorium, and sting apparatus
Fig. 12: Male wings of Opamyrma hungvuong, nontype (Dai19iii2019-029, Son La, Vietnam). (A) forewing in dorsal view; (B) hind wing in dorsal view. Abbreviations: 1A = first anal vein; Bc = basal cell; C = costal vein; Cc = costal cell; Cu = cubital vein; Mc1 = marginal cell 1; R = radial vein; Rs = radial sector; Sbc = subbasal cell; Sc = subcostal vein; Sdc1 = subdiscal cell 1; Smc = submarginal cell.
Fig. 2 in Unveiling the morphology of the Oriental rare monotypic ant genus Opamyrma YAMANE, BUI & EGUCHI, 2008 (Hymenoptera: Formicidae: Leptanillinae) and its evolutionary implications, with first descriptions of the male, larva, tentorium, and sting apparatus
Fig. 2: Scanning electron microscope images of cephalic parts of Opamyrma hungvuong worker, nontype (AKY05vii17-06, China, Guangxi). (A) anterior part of head in frontal view; (B) cranium in ventral view; (C) right mandible in dorsal view; (D) right hypostomal process in lateral view; (E) left mandible in ventral view; (F) labrum in outer view. Abbreviations: Ctl = canthellus; Hysp = hypostomal process; Occ = occipital carina; Lbr = labrum; Lps = labral peg-like seta; Mdl = mandalus; Mps = mandibular peg-like seta; Pat = preapical tooth; Ptg = peritorular groove; Ptp = posterior tentorial pit; Sca = supraclypeal area.
Fig. 6 in Unveiling the morphology of the Oriental rare monotypic ant genus Opamyrma YAMANE, BUI & EGUCHI, 2008 (Hymenoptera: Formicidae: Leptanillinae) and its evolutionary implications, with first descriptions of the male, larva, tentorium, and sting apparatus
Fig. 6: Scanning electron microscope images of mesosoma of Opamyrma hungvuong worker, nontype (AKY05vii17-06, China, Guangxi). (A) whole mesosoma in lateral view; (B) anterior articulation of mesonotum in lateral view, prothorax removed; (C) whole mesosoma in dorsal view; (D) whole mesosoma in ventral view, all legs removed; (E) metapleuron and propodeum in lateral view; (F) prosternite in ventral view, propleurae and prolegs removed. Abbreviations: Mgo = metapleural gland orifice; Mlf = metapleural longitudinal flange; Msg = mesonotal groove; Mstp = mesosternal pit; Mtsp = metanotal spiracle; Pcc = procoxal cavity; Pdl = propodeal lobe.
Fig.10 in Unveiling the morphology of the Oriental rare monotypic ant genus Opamyrma YAMANE, BUI & EGUCHI, 2008 (Hymenoptera: Formicidae: Leptanillinae) and its evolutionary implications, with first descriptions of the male, larva, tentorium, and sting apparatus
Fig.10: Opamyrma hungvuong queen, nontype (Dai19iii2019-029, Son La, Vietnam). (A) head in full-face view; (B) body in lateral view; (C) head in ventral view; (D) head and mesosoma in dorsal view; (E) Scanning electron microscope image of mesosoma in lateral view; (F) Scanning electron microscope image (SEM) of meso- and metanotum in dorsal view; (G) forewing in dorsal view; (H) hindwing in dorsal view. Abbreviations: Axa = axilla; Axu = axillula; Msg = mesonotal groove; Occ = occipital carina; Pgr = postgenal ridge; Pl = parapsidal line; Prx = preaxilla; Rs = radial sector; Scs = scutoscutellar sulcus.
Fig. 8 in Unveiling the morphology of the Oriental rare monotypic ant genus Opamyrma YAMANE, BUI & EGUCHI, 2008 (Hymenoptera: Formicidae: Leptanillinae) and its evolutionary implications, with first descriptions of the male, larva, tentorium, and sting apparatus
Fig. 8: Scanning electron microscope images of metasoma of Opamyrma hungvuong worker, nontype (AKY05vii17-06, China, Guangxi). (A) petiole in lateral view; (B) petiole in ventral view; (C) helcium in anterior view; (D) helcium in ventral view; (E) pretergite of abdominal segment IV in dorsal view; (F) gaster in lateral view; (G) gaster in ventral view. Abbreviations: Absg = abdominal segment; Prsn = presternite; Prtg = pretergite; Ptlt = petiolar laterotergite; Ptsn = petiolar sternite; Tss = tergosternal suture.
Figure 1 in How survival and food intake of tri-spine horseshoe crabsı Tachypleus tridentatus respond to thermal variation: implications for understanding its distribution limit
Figure 1. Global distribution of T. tridentatus as reported by previous literature, and the regional changes of sea surface temperature (SST) in (a) summer and (b) winter. Note the three occurrence reports outside their geographic range: (1) a non-native population from Chubu Region, Central Japan; (2) an escape population from Okinawa Prefecture, Japan due to broken nets during transportation; (3) a sighting of single female from Jeju, South Korea, which was not associated with a known spawning or juvenile nursery habitat.
Comparing power-system- and user-oriented battery electric vehicle charging representation and its implications on energy system modeling
<p>This supplementary material includes data and code for the research described in the paper "Comparing power-system- and user-oriented battery electric vehicle charging representation and its implications on energy system modeling". The code containts an interface between the output files of the agent-based simulation model CURRENT and the energy system optimization model REMix as well as some scripts for analyzing REMix results. The data folder contains input data for REMix, the complete list of all model runs analyzed in the paper in the GAMS format .gdx as well as Excel files containing annual results of the sensitivity runs and respective pivot tables and figures for respective analysis.</p>
FIGURE 7 in The complete mitochondrial genome of Zicrona caerulea (Linnaeus) (Hemiptera: Pentatomidae: Asopinae) and its phylogenetic implications
FIGURE 7. Inferred phylogenetic relationships among Pentatomoidea based on the concatenated nucleotide sequences of 13 mitochondrial protein-coding genes using maximum likelihood (ML) (quadrangles: Phyllocephalinae; circles: Pentatominae; heart: Podopinae; pentagons: Asopinae). Numbers on branches are bootstrap percentages.
Fig. 4. Bivariate graphs for the Smilodon populator specimen MNHN-P 957. A in An extremely large saber-tooth cat skull from Uruguay (late Pleistocene -early Holocene, Dolores Formation): body size and paleobiological implications
Fig. 4. Bivariate graphs for the Smilodon populator specimen MNHN-P 957. A, PM3 transverse diameter (PM3ML) versus PM3 anteroposterior diameter (PM3AP); B, PM4 transverse diameter (PM4ML) versus PM4 anteroposterior diameter (PM4AP). Data from different sources (see Material and methods).
Figure 3. Bivariate graphs for the Smilodon populator specimen MNHN-P 957. A in An extremely large saber-tooth cat skull from Uruguay (late Pleistocene -early Holocene, Dolores Formation): body size and paleobiological implications
Figure 3. Bivariate graphs for the Smilodon populator specimen MNHN-P 957. A, zygomatic width (ZW) versus condylobasal length (CBL); B, canine transverse diam- eter (CML) versus canine anteroposterior diameter (CAP). Data from different sources (see Material and methods).
Fig. 9 in Fused and vaulted nasals of tyrannosaurid dinosaurs: Implications for cranial strength and feeding mechanics
Fig. 9. Comparison of theropod nasal strengths at multiple transverse sections. Horizontal (Iy) and vertical (Iz) second moments of area of nasal cross−sections of Allosaurus fragilis (upper two graphs) and tyrannosaurids (lower two graphs). Second moments of area are proportional to lateral (Iy) and vertical (Iz) bending strengths. X−axes of graphs show relative position of slices along the long axes of the bones: 0.0 is posterior and 1.0 anterior.
Fig. 6 in Fused and vaulted nasals of tyrannosaurid dinosaurs: Implications for cranial strength and feeding mechanics
Fig. 6. Geometry used to compute the area, centroid, and second moments of area of a nasal cross−section (from middle region of fused Tyrannosaurus rex nasals: TMP 98.86.01; cast of BHI 2033). A. Decomposition of the cross−section to compute area by summing areas of triangles. Small "+"s are centroids of individual triangles. Large "+" is the centroid for the complete section. B. Cross−section partitioned into horizontal and vertical strips of known area and position, used to calculate second moments of area.
Fig. 5 in Fused and vaulted nasals of tyrannosaurid dinosaurs: Implications for cranial strength and feeding mechanics
Fig. 5. CT cross sections and reconstructions of Allosaurus fragilis nasals: A, largest (UUVP 1663/UMNH VP 9146); B, midsize (UUVP 1913/ UMNH VP 9144); and C, smallest (UUVP 10854/UMNHVP 7784). Anterior is to the right. Cross sections are from the strongly pneumatized regions of the nasals, at positions indicated by the dashed lines. The slices are normalized to the same size to show the relative degree of pneumatic excavation, evident despite mineral infilling in some sections. Reconstructions are in lateral views and in dorsal views with single left or right specimens mirrored to replicate complete pairs. Specimen B is broken over the posterior part of the external nares. Scale bar 10 cm.
Fig. 4 in Fused and vaulted nasals of tyrannosaurid dinosaurs: Implications for cranial strength and feeding mechanics
Fig. 4. CT reconstructions of tyrannosaurid nasals in side and top views. Anterior is to the right. A. Tyrannosaurus rex (TMP 98.86.01; cast of BHI 2033). B. Daspletosaurus torosus (TMP 98.48.1). C. Albertosaurus sarcophagus (TMP 2000.12.1). D. Adult Gorgosaurus libratus (TMP 86.64.1). E. Juvenile Gorgosaurus libratus (TMP 86.144.1). Scale bars 15 cm.
Fig. 1 in Fused and vaulted nasals of tyrannosaurid dinosaurs: Implications for cranial strength and feeding mechanics
Fig. 1. Comparison of cranial and nasal morphology of: A, the tyrannosaurid Tyrannosaurus rex (TMP 98.86.01; cast of BHI 2033) and B, the carnosaur Allosaurus fragilis (UUVP 1663/UMNH VP 9146; mirrored to depict a complete pair). Scale axes for crania are in meters. Nasals in their life positions are highlighted in lateral and dorsal cranial views, and rendered in oblique view (not to scale). The T. rex nasals are tall, vaulted, and fused, while the A. fragilis nasals are lower and unfused.
Data and Code to support COVID-19 - exploring the implications of long-term condition type and extent of multimorbidity on years of life lost: a modelling study
<p>Data and code to support paper published in Wellcome Open research on years of life lost among people who died with COVID-19.</p>
Data for vertebrate scavenger species composition on Nantucket Island, Massachusetts and implications for Nicrophorus americanus Olivier (American burying beetle) reintroduction
<p>Abstract: We surveyed scavenger species on Nantucket Island, MA, using motion-activated wildlife cameras baited with carcasses of either a Mus musculus domesticus (House Mouse) or Colinus virginianus (Bobwhite Quail) in the summer of 2016. We aimed to identify vertebrate scavenger species, measure how long carcasses remained available, and examine differences in carrion consumption between grassland and shrubland vegetation types. This information is important for management decisions concerning a reintroduced population of a federally endangered obligate scavenger, Nicrophorus americanus (American Burying Beetle), on Nantucket Island. Carcasses were removed or consumed within 2.7 ± 1.8 d, and vertebrates removed the carcass in 74% of trials. Carcasses persisted for similar lengths of time between the 2 vegetation types, but avian scavengers were significantly more common on Bobwhite Quail carcasses in grassland, and mammalian scavengers were significantly more common on House Mouse carcasses in shrubland habitats. Avian species appear to be significant competitors for carrion appropriate for American Burying beetle reproduction.</p> <p>This project was partly funded by grant #15-233 from the <a href="https://www.norcrosswildlife.org/">Norcross Wildlife Foundation</a>. </p> <p>File descriptions:<br> allCameraData.csv- Cleaned raw camera data. 2015 data from a pilot study and 2016 data are what was used for the publication.<br> dataDictionary.csv- Data dictionary for all csv files<br> figure2_goodnessOfFitTests.R- R code to create figure 2 and run goodness of fit and post hoc tests<br> quadplotper.csv- Data used by figure2_goodnessOfFitTests.R to create figure<br> resultsSummarized.csv- Authors' determinations of what species removed carrion</p>
FIGURE 24. A–B in Middle Permian (Roadian) gastropods from the Khao Khad Formation, Central Thailand: Implications for palaeogeography of the Indochina Terrane
FIGURE 24. A–B, Palaeostylus sp., ESKU-19-LP 7. C–D, Pseudozygopleura? sp., ESKU-19-LP 63. Scale bars represent: 1 mm (A–B); 2 mm (C–D).
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.