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Figure 1 in Osteology and phylogenetic position of the diminutive 'microsaur' Odonterpeton triangulare from the Pennsylvanian of Linton, Ohio, and major features of recumbirostran phylogeny
Figure 1. Photographs of the part (USNM PAL 4465) and counterpart (USNM PAL 4467) of the holotype of Odonterpeton triangulare. A, C, skeleton exposed in dorsal view (A) and ventral view (C). B, D, resin casts of the skeleton exposed in dorsal view (B) and ventral view (D).
Figure 3 in Osteology and phylogenetic position of the diminutive 'microsaur' Odonterpeton triangulare from the Pennsylvanian of Linton, Ohio, and major features of recumbirostran phylogeny
Figure 3. Photographs and labelled drawings of the skull of the holotype of Odonterpeton triangulare. A, B, dorsal view (USNM PAL 4465). C, D, ventral view of the skull and the anterior end of the cervical region (USNM PAL 4467). See Material and Methods for anatomical abbreviations.
Figure 6 in Osteology and phylogenetic position of the diminutive 'microsaur' Odonterpeton triangulare from the Pennsylvanian of Linton, Ohio, and major features of recumbirostran phylogeny
Figure 6. Palatal views of selected early amniotes, including recumbirostrans, focusing on the structured pterygoid (peach coloured). A, palate of the early captorhinid eureptile, Captorhinus, showing a triradiate pterygoid with a distinct, posteroventrally descending and tooth-bearing transverse flange of the pterygoid (Fox & Bowman, 1966). B, palate of an early-diverging synapsid, Eothyris, showing a triradiate pterygoid with a weakly posteriorly oriented, ventrally descending and tooth-bearing transverse flange of the pterygoid (Reisz et al., 2009). C, palate of an early eureptile, Protorothyris, showing a triradiate pterygoid with an almost straight, ventrally descending and tooth-bearing transverse flange of the pterygoid (Clark & Carroll, 1973). D, palate of an early eureptile, Paleothyris, showing a triradiate pterygoid with a weakly posteriorly oriented, ventrally descending and tooth-bearing transverse flange of the pterygoid (Carroll, 1969). E, palate of an early parareptile, Acleistorhinus, showing a triradiate pterygoid with a nearly straight, perhaps slightly anteriorly canted, ventrally descending and tooth-bearing transverse flange of the pterygoid (deBraga & Reisz, 1996). F, palate of the araeoscelid eureptile Petrolacosaurus, showing a less distinct, anteriorly oriented and tooth-bearing transverse flange of the pterygoid (Reisz, 1977). G, palate of a putative captorhinid reptile, Opisthodontosaurus, showing a triradiate pterygoid with a somewhat straight, shallowly descending, lightly denticulated, transverse flange of the pterygoid (Reisz et al., 2015).
FIG. 3 in A Long-term Demographic Study of a Spotted Salamander (Ambŋstoma maculatum) Population in Central Ohio
FIG. 3.—Relationships between percent mass loss and number of days spent in Taylor–Ochs Pond, Ohio, for individually marked female (R2 ¼ 0.57, P ¼ 0.001; y ¼ 1.25x þ 6.76) and male (R2 ¼ 0.18, P ¼ 0.001, y ¼ 0.29x þ 3.39) Ambŋstoma maculatum sampled from 2005 to 2014.
F. 1 in A Long-term Demographic Study of a Spotted Salamander (Ambŋstoma maculatum) Population in Central Ohio
F. 1.—Numbers of (a) breeding Ambŋstoma maculatum adults (R2 ¼ IG 0.46, P ¼ 0.03), (b) split by sex (females, R2 ¼ 0.02, P ¼ 0.67; males, R2 ¼ 0.68, P ¼ 0.003), and (c) counts of breeding females plotted alongside egg mass counts and numbers of emerging juveniles from 2005 to 2014 in Taylor–Ochs Pond, Ohio. Numbers near the bottom of (b) reflect sex ratios (male:female), and numbers near the bottom of (c) reflect recruitment rates (emerging juveniles per breeding female) for each year. Significant negative linear relationships of overall breeding adults (a) and breeding males (b) over time are represented by the equations y ¼ 46.1x þ 93246.0 and y ¼ 41.6x þ 84148.9, respectively.
FIG. 2 in A Long-term Demographic Study of a Spotted Salamander (Ambŋstoma maculatum) Population in Central Ohio
FIG. 2.—Mean values (±1 SE) for mass (a) and snout–vent length (SVL, b) of inbound female and male Ambŋstoma maculatum sampled from 2005 to 2014 in Taylor–Ochs Pond, Ohio. See Table 3 for the sample size contributing to each depicted value. In all years, for both body-size indicators, females were larger than males (P <0.05). For simplicity, only differences among years (sexes combined) are reflected by different letter(s) above each pair of bars.
Species diagnosis tables for: Crinoids from the Wooster Shale Member of the Cuyahoga Formation, Carboniferous (Mississippian, Tournaisian) of Northeastern Ohio
<p>Nine crinoids are described from the Wooster Shale Member of the Cuyahoga Formation from Wayne and Ashland counties, Ohio, USA. Identifiable elements of the fauna include five camerate crinoids, one flexible crinoid, and three other eucladid crinoids. Five new species are described, including <em>Cactocrinus</em> <em>woosterensis</em> n. sp., <em>Cusacrinus</em> <em>brushi</em> n. sp., <em>Agaricocrinus</em> <em>murphyi</em> n. sp., <em>Decadocrinus</em> <em>laevis</em> n. sp., and <em>Decadocrinus</em> <em>inordinatus</em> n. sp. Overall, the distribution of crinoid clades in the Wooster Shale is similar to that of the stratigraphically lower Meadville Shale Member of the Cuyahoga Formation, although less diverse and with only one species (<em>Cyathocrinites</em> <em>simplex</em>) in common. Many of the Wooster Shale crinoids are completely or partially preserved with siderite in either nodules or within siderite beds. These crinoids are commonly preserved in trauma postures, which is characteristic of burial in episodic high turbulence events. The paleoenvironments and taxa of the two Cuyahoga Formation crinoid faunas more closely resemble Viséan faunas in siliciclastic settings than typical carbonate faunas of the Tournaisian. Supplemental tables included here are species diagnostic tables listing characters for differentiating species in the following Mississippian crinoid (Phylum Echinodermata) genera: <em>Agaricocrinus</em>, <em>Cactocrinus</em>, <em>Cusacrinus</em>, and <em>Decadocrinus</em>. </p>
Supplementary data for: A Silurian (Homerian) pelmatozoan echinoderm fauna from west-central Ohio
<p>A diverse echinoderm fauna lived in reef and non-reef Silurian facies of the upper Midwestern United States. However, these faunas are dominantly preserved in dolostones with fossils preserved only as molds and casts, and fossils from dolostone facies have not been documented to the extent of Silurian crinoids in non-dolostone strata. Herein, an echinoderm fauna is described from the dolostones of the Cedarville Member of the Laurel Limestone (Wenlock, Homerian) from the Pepcon Quarry in west-central Ohio. The described fauna contains blastoids, hemicosmitoids, and crinoids, including <em>Troosticrinus</em> <em>subcylindricus</em> (Hall and Whitfield, 1875); <em>Caryocrinites</em> sp.; an unidentifiable diplobathrid camerate, <em>Periechocrinus</em> <em>tennesseensis</em> (Hall and Whitfield, 1875); <em>Periechocrinus</em> <em>egani</em>? Miller, 1881; <em>Stiptocrinus</em> <em>farringtoni</em> (Slocom, 1908); <em>Calliocrinus</em> <em>primibrachialis</em> Busch, 1943; <em>Calliocrinus</em> <em>popplemani</em> n. sp.; <em>Calliocrinus</em> <em>hadros</em> n. sp.; and <em>Lecanocrinus</em> sp. Generic concepts for the Eucalyptocrinitidae are clarified; and, surprisingly, Eucalyptocrinites is absent from this fauna.</p>
Ohio Patient Navigator Research Program
ClinicalTrials.gov study NCT01569672. IPD Sharing: NO. Countries: 1. Publications: 4.
HPV Self-Test Intervention in Ohio Appalachia
ClinicalTrials.gov study NCT02460237. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Ohio State University Multiple Myeloma and Amyloidosis Data Registry and Sample Resource
ClinicalTrials.gov study NCT01408225. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Beating Lung Cancer in Ohio Protocol in Improving Survival in Patients with Stage IV Non-Small Cell Lung Cancer
ClinicalTrials.gov study NCT03199651. IPD Sharing: NO. Countries: 1. Publications: 8.
Appeal of Nicotine Pouches Versus Cigarettes in the Ohio Appalachia Population
ClinicalTrials.gov study NCT05236894. IPD Sharing: NO. Countries: 1. Publications: 2.
Ohio Colorectal Cancer Prevention Initiative
ClinicalTrials.gov study NCT01850654. IPD Sharing: Not stated. Countries: 1. Publications: 4.
Web-based Education on Oral Cancer for Primary Care Physicians in Ohio
ClinicalTrials.gov study NCT01424358. IPD Sharing: Not stated. Countries: 1. Publications: 8.
Zoonotic Influenza Infections of Swine Origin at Ohio Agricultural Fairs
ClinicalTrials.gov study NCT02124096. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Historical trends in the nitrogen requirement of corn over 45 years in Ohio
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Data from: New information on Titanichthys (Placodermi: Arthrodira) from the Cleveland shale (upper devonian) of Ohio, USA
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Data from: Butterfly abundance declines over 20 years of systematic monitoring in Ohio, USA
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Data from: Contextualizing macroecological laws: A big data analysis on electrofishing and allometric scalings in Ohio, USA
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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.
Annotated Behaviour and Observability Dataset (ABODe)
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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.