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Text-fig. 6. Transmitted light microphotographs of permineralized wood from Govone. a, b: cf. Cupressinoxylon sp., radial section, MGPT-PU141105, a – nodular end of ray parenchyma (arrow), b – thick and pitted horizontal walls of ray parenchyma (arrow). c–f: Pinaceae gen. et sp. indet., MGPT-PU141107, c – abnormal discoloration due to ecological disruptions (radial section), d – rays up to 10 cells high, uniseriate, partly biseriate (black arrow), intercellular spaces observed (white arrows) (tangential section), e – large, thick-walled axial resin canal with more than 9 epithelial cells observed, axial resin canal diameter>60 Μm (transverse section), f – spiral thickenings due to compression (white arrow) (radial section). in Remains Of A Subtropical Humid Forest In A Messinian Evaporitebearing Succession At Govone, Northwestern Italy - Preliminary Results
Text-fig. 6. Transmitted light microphotographs of permineralized wood from Govone. a, b: cf. Cupressinoxylon sp., radial section, MGPT-PU141105, a – nodular end of ray parenchyma (arrow), b – thick and pitted horizontal walls of ray parenchyma (arrow). c–f: Pinaceae gen. et sp. indet., MGPT-PU141107, c – abnormal discoloration due to ecological disruptions (radial section), d – rays up to 10 cells high, uniseriate, partly biseriate (black arrow), intercellular spaces observed (white arrows) (tangential section), e – large, thick-walled axial resin canal with more than 9 epithelial cells observed, axial resin canal diameter>60 Μm (transverse section), f – spiral thickenings due to compression (white arrow) (radial section).
Text-fig. 4. Juglandaceae Carya (a–w). Scale bars = 1 cm. a–d: USNM PAL 772352, reflected light, palladium coated. a: Obliquelateral view of nut, apex up. b: Basal view with damage to left and clear depiction of meridional grooves. c, d: Two lateral views oriented about 130° from each other and avoiding the area of damage; the meridional grooves clear in (c). e–l: USNM PAL 772350. e: Intact nut, lateral view, apex up, reflected light. f: One half of split nut revealing in situ chalcedony locule cast, reflected light. g–k: Virtual sections from micro-CT data. g: Longitudinal section parallel to the exposed face in (f). h: Longitudinal section at 90° from (g). i: Transverse section in apical 1/3 showing locule bracketed by C-shaped lacunae (arrows). j: Equatorial transverse section showing two lobes of the locule separated by primary septum, lacuna evident below as white line. k: Transverse section near base in The Early Middle Eocene Wagon Bed Carpoflora Of Central Wyoming, U.S.A.
Text-fig. 4. Juglandaceae Carya (a–w). Scale bars = 1 cm. a–d: USNM PAL 772352, reflected light, palladium coated. a: Obliquelateral view of nut, apex up. b: Basal view with damage to left and clear depiction of meridional grooves. c, d: Two lateral views oriented about 130° from each other and avoiding the area of damage; the meridional grooves clear in (c). e–l: USNM PAL 772350. e: Intact nut, lateral view, apex up, reflected light. f: One half of split nut revealing in situ chalcedony locule cast, reflected light. g–k: Virtual sections from micro-CT data. g: Longitudinal section parallel to the exposed face in (f). h: Longitudinal section at 90° from (g). i: Transverse section in apical 1/3 showing locule bracketed by C-shaped lacunae (arrows). j: Equatorial transverse section showing two lobes of the locule separated by primary septum, lacuna evident below as white line. k: Transverse section near base
FIGURE 7 in A New Species of the New Zealand Endemic Genus Actenonyx White, 1846 (Coleoptera: Carabidae: Odacanthini) with Notes on Variation, Distribution, and Habitat
FIGURE 7. Photographs of habitat for Actenonyx aotearoa sp. nov. A. Glaciated valley at east end of Homer Tunnel, Fiordlands National Park, South Island, view looking north; B. Snowmelt streams at east end of Homer Tunnel, just south of tunnel entrance.
FIGURE 2 in A New Species of the New Zealand Endemic Genus Actenonyx White, 1846 (Coleoptera: Carabidae: Odacanthini) with Notes on Variation, Distribution, and Habitat
FIGURE 2. Male genitalia of Actenonyx species. A and B. A. bembidioides White (South Island, Southland, Te Anau Downs, Mistletoe Creek, 216 m); C and D. A. aotearoa sp. nov. (South Island, Fiordlands National Park, east end of Homer Tunnel, 915m). A and C. Dorsal aspect; B and D. Left lateral aspect. Scale line = 0.5 mm.
FIGURE 6 in A New Species of the New Zealand Endemic Genus Actenonyx White, 1846 (Coleoptera: Carabidae: Odacanthini) with Notes on Variation, Distribution, and Habitat
FIGURE 6. Photograph of habitat for Actenonyx bembidioides White. Arrow River at Arrowtown, Otago, South Island.
FIGURE 5 in A New Species of the New Zealand Endemic Genus Actenonyx White, 1846 (Coleoptera: Carabidae: Odacanthini) with Notes on Variation, Distribution, and Habitat
FIGURE 5. Map showing distribution records for specimens of Actenonyx aotearoa sp. nov. examined for this study (red circle = type locality; blue circles = localities where specimens have pronotal lateral setae; black circles = other localities). Scale line = 200 km.
FIGURE 1 in A New Species of the New Zealand Endemic Genus Actenonyx White, 1846 (Coleoptera: Carabidae: Odacanthini) with Notes on Variation, Distribution, and Habitat
FIGURE 1. Dorsal habitus of Actenonyx species. A. A. bembidioides White (South Island, Southland, Te Anau Downs, Mistletoe Creek, 216 m); B. A. aotearoa sp. nov. (South Island, Fiordlands National Park, east end of Homer Tunnel, 915m). Scale lines = 1.0 mm.
FIGURE 4 in A New Species of the New Zealand Endemic Genus Actenonyx White, 1846 (Coleoptera: Carabidae: Odacanthini) with Notes on Variation, Distribution, and Habitat
FIGURE 4. Map showing distribution records for specimens of Actenonyx bembidioides White examined for this study (red circle = type locality; black circles = other localities). Scale line = 200 km.
FIGURE 3. Female genitalia and reproductive tract. A and C. A in A New Species of the New Zealand Endemic Genus Actenonyx White, 1846 (Coleoptera: Carabidae: Odacanthini) with Notes on Variation, Distribution, and Habitat
FIGURE 3. Female genitalia and reproductive tract. A and C. A. bembidioides White (South Island, Southland, Te Anau Downs, Mistletoe Creek, 216 m); B and D. A. aotearoa sp. nov. (South Island, Fiordlands National Park, east end of Homer Tunnel, 915m); A and B. Tergite IX, dorsal aspect; C and D. Genital capsule and reproductive tract; bc = bursa copulatrix; co = common oviduct; gc1 = gonocoxite 1; gc2 = gonocoxite 2; sbb = spermathecal basal bulb; sg = spermathecal gland; sgd =spermathecal gland duct. Scale lines = 0.5 mm.
Рис. 9. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста в прироΑном парке «Шереметьевский» в 2018 г. Fig. 9. Distribution of nests of the Oriental White Stork in the Sheremetyevsky Nature Park in 2018 in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 9. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста в прироΑном парке «Шереметьевский» в 2018 г. Fig. 9. Distribution of nests of the Oriental White Stork in the Sheremetyevsky Nature Park in 2018
Рис. 7. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста в заказнике «Аистиный» и его бΛижайших окрестностях по состоянию на 2018 г. Fig. 7. Distribution of nests of the Oriental White Stork in the Aistiny Reserve and its immediate vicinity as of 2018 in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 7. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста в заказнике «Аистиный» и его бΛижайших окрестностях по состоянию на 2018 г. Fig. 7. Distribution of nests of the Oriental White Stork in the Aistiny Reserve and its immediate vicinity as of 2018
Рис. 1. РаспреΑеΛение кΛючевых мест гнезΑования ΑаΛьневосточного аиста в Хабаровском крае в 1999–2000 гг. (по: Δарман и Αр. 2000b; Сурмач, Шибаев 2000) Fig. 1. Distribution of key nesting sites of the Oriental White Stork in the Khabarovsk Territory in 1999–2000 (based on: Darmanet al. 2000b; Surmach, Shibaev 2000) in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 1. РаспреΑеΛение кΛючевых мест гнезΑования ΑаΛьневосточного аиста в Хабаровском крае в 1999–2000 гг. (по: Δарман и Αр. 2000b; Сурмач, Шибаев 2000) Fig. 1. Distribution of key nesting sites of the Oriental White Stork in the Khabarovsk Territory in 1999–2000 (based on: Darmanet al. 2000b; Surmach, Shibaev 2000)
Рис. 4. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста на воΑно-боΛотных угоΑьях оз. БоΛонь в 2018 г. Fig. 4. Distribution of nests of the Oriental White Stork in the wetlands of Lake Bolon in 2018 in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 4. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста на воΑно-боΛотных угоΑьях оз. БоΛонь в 2018 г. Fig. 4. Distribution of nests of the Oriental White Stork in the wetlands of Lake Bolon in 2018
Рис. 5. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста на о. БоΛьшой Уссурийский в 2018 г. Fig. 5. Distribution of nests of the Oriental White Stork on the Bolshoi Ussuriisky island in 2018 in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 5. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста на о. БоΛьшой Уссурийский в 2018 г. Fig. 5. Distribution of nests of the Oriental White Stork on the Bolshoi Ussuriisky island in 2018
Рис. 11. Выброшенный из гнезΑа птенец ΑаΛьневосточного аиста в заказнике «Муравьевский» в Амурской обΛасти, май 2010 г. Фото М. Н. Кочерга Fig. 11. A Oriental White Stork chick thrown out of the nest in the Muravyevsky Nature Reserve in the Amur Region, May 2010. Photo by M. N. Kocherga in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 11. Выброшенный из гнезΑа птенец ΑаΛьневосточного аиста в заказнике «Муравьевский» в Амурской обΛасти, май 2010 г. Фото М. Н. Кочерга Fig. 11. A Oriental White Stork chick thrown out of the nest in the Muravyevsky Nature Reserve in the Amur Region, May 2010. Photo by M. N. Kocherga
Рис. 10. Выброшенный из гнезΑа птенец ΑаΛьневосточного аиста в прироΑном парке «Шереметьевский», май 2018 г. Фото А. Δ. Степных Fig. 10. A Oriental White Stork chick thrown out of the nest in the Sheremetyevsky Nature Park, May 2018. Photo by A. D. Stepnykh in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 10. Выброшенный из гнезΑа птенец ΑаΛьневосточного аиста в прироΑном парке «Шереметьевский», май 2018 г. Фото А. Δ. Степных Fig. 10. A Oriental White Stork chick thrown out of the nest in the Sheremetyevsky Nature Park, May 2018. Photo by A. D. Stepnykh
Рис. 3. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста на воΑно-боΛотных угоΑьях оз. БоΛонь по материаΛам авиаучетов: 1999 г. — треугоΛьник (по: Δарман, АнΑронов, Хигучи и Αр. 2000); 2004 г. — звезΑочка; 2005 г. — кружок Fig. 3. Distribution of nests of the Oriental White Stork in the wetlands of Lake Bolon based on aerial surveys: 1999 — triangle (based on: Darman et al. 2000a); 2004 — asterisk; 2005 — circle in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 3. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста на воΑно-боΛотных угоΑьях оз. БоΛонь по материаΛам авиаучетов: 1999 г. — треугоΛьник (по: Δарман, АнΑронов, Хигучи и Αр. 2000); 2004 г. — звезΑочка; 2005 г. — кружок Fig. 3. Distribution of nests of the Oriental White Stork in the wetlands of Lake Bolon based on aerial surveys: 1999 — triangle (based on: Darman et al. 2000a); 2004 — asterisk; 2005 — circle
Рис. 2. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста в Хабаровском крае по состоянию на 2018 г. Fig. 2. Distribution of nests of the Oriental White Stork in the Khabarovsk Territory as of 2018 in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 2. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста в Хабаровском крае по состоянию на 2018 г. Fig. 2. Distribution of nests of the Oriental White Stork in the Khabarovsk Territory as of 2018
Рис. 1. Раковины Mya truncata (А–Г) (Белое море) и Laternula elliptica (А'–Г') (Зал. Прюдс): А, А' – обЩий вид; Б, Г' – внутреннЯЯ поверхность левых створок; В, В' – вид хондрофора со стороны дорсального краЯ; Г, Б' – внутреннЯЯ поверхность правых створок. ОбоЗначениЯ: пК – передний край раковины; ЗК – Задний край; дК – дорсальный край; м – макушка; мщ – макушечнаЯ (умбональнаЯ) Щель; Кс – концентрическаЯ скульптура; сКп – складки периостракума; хр – хондрофор; ппЛ – поддерживаюЩаЯ пластинка; син – синус; ОмЗ – отпечаток мускула-ЗамыкателЯ. Fig. 1. Shells of Mya truncata (А–Г) (White Sea) and Laternula elliptica (А'–Г') (Prydz Bay): A, A' – general view; Б, Г' – internal view of left valves; В, В' – dorsal view on chondrophores; Г, Б' – internal view of right valves. Notes: пК – anterior margin; ЗК – posterior margin; дК – dorsal margin; м – umbo; мщ – umbonal crack; Кс – concentric sculpture; сКп – periostracal wrinkles; хр – chondrophore; ппЛ – buttress; син – sinus; ОмЗ – trace of retractor muscle. in Species of warm-water origin Laternula elliptica (King, 1832) (Mollusca: Bivalvia: Laternulidae), a widespread mollusk in recent Antarctica
Рис. 1. Раковины Mya truncata (А–Г) (Белое море) и Laternula elliptica (А'–Г') (Зал. Прюдс): А, А' – обЩий вид; Б, Г' – внутреннЯЯ поверхность левых створок; В, В' – вид хондрофора со стороны дорсального краЯ; Г, Б' – внутреннЯЯ поверхность правых створок. ОбоЗначениЯ: пК – передний край раковины; ЗК – Задний край; дК – дорсальный край; м – макушка; мщ – макушечнаЯ (умбональнаЯ) Щель; Кс – концентрическаЯ скульптура; сКп – складки периостракума; хр – хондрофор; ппЛ – поддерживаюЩаЯ пластинка; син – синус; ОмЗ – отпечаток мускула-ЗамыкателЯ. Fig. 1. Shells of Mya truncata (А–Г) (White Sea) and Laternula elliptica (А'–Г') (Prydz Bay): A, A' – general view; Б, Г' – internal view of left valves; В, В' – dorsal view on chondrophores; Г, Б' – internal view of right valves. Notes: пК – anterior margin; ЗК – posterior margin; дК – dorsal margin; м – umbo; мщ – umbonal crack; Кс – concentric sculpture; сКп – periostracal wrinkles; хр – chondrophore; ппЛ – buttress; син – sinus; ОмЗ – trace of retractor muscle.
Lidar Scans of the White River near Worthington, Indiana, U.S.A.: Supporting data for Martin et al. (2024)
<p>Supporting data for the manuscript "Four years of meander-bend evolution captured by drone-based lidar reveals lack of width maintenance on the White River, Indiana, USA" by Harrison K Martin, Douglas A Edmonds, and Quinn W Lewis. As of June 2024, the manuscript has been published in the <em>Journal of Geophysical Research: Earth Surface</em> and is available here: <a href="https://doi.org/10.1029/2023JF007574">https://doi.org/10.1029/2023JF007574</a>. You can find additional details in the Supplemental Information for that paper.</p> <p>Also of interest may be another recently published manuscript (in <em>Earth Surface Processes and Landforms</em>) on a pair of failed dams from central Michigan where we quantified topographic change using lidar change detection. On that study, we compared an airborne pre-flood survey to three post-flood drone-based lidar surveys we collected. The methods employed were not identical to this study (namely, there we used a point cloud to point cloud differencing method rather than the differences of DEMs used here), but there could be some helpful information in that manuscript's Supporting Info. It's available here: <a href="https://doi.org/10.1002/esp.5855">https://doi.org/10.1002/esp.5855</a>.</p> <p> </p> <p>In this repository you will find 22 bare-earth Digital Elevation Models (DEMs) of a single river bend on the meandering White River near Worthington, IN. The scans were collected over a period of ~4.5 years between April 2018 and November 2022 -- not coincidentally, nearly the same span of time as my PhD. Each DEM attempts to present the bare earth as if the vegetation were not present; the algorithms and trimming do a better job on tall, forested canopies (such as the northeastern-most part of the point bar) than on short, dense, shrubby grasses (such as certain parts of the cutbank or where crops were grown). The vegetation noise and artifacts will be the greatest in the summer months and the least in the winter. The point bar surface was always well-resolved. The actual river/water surface itself was masked out manually for each of the 22 scans, with null values defined for these and other no-data areas. The filename of each scan describes the date of collection. The cell size for each raster is 25 cm and was created by exporting a triangular lattice constructed from a ground-classified point cloud with a maximum length of 10 meters. Because of this, areas with very low point density (such as the outer boundaries of each scan, outside of the areas where we wanted to measure geomorphic changes) appear to be made of large triangles, and should not be trusted. The CRS for each is NAD83 / UTM zone 16N [https://epsg.io/26916].</p> <p> </p> <p>Please do not hesitate to reach out with any questions, requests, etc! I'm pretty responsive by email (hkm@caltech.edu) and website form (https://harrison.studies.rocks). If you have any questions about the methods, setting up your own drone-based lidar program, or are struggling with some of the arcane software and quirks of this sort of workflow... there is a chance that I've struggled through it before and am happy to share whatever I have learned!</p> <p> </p> <p>Thanks for stopping by!</p> <p> </p> <p>Acknowledgements:</p> <p>A big thanks is owed to Steve Scott of Indiana University, our stalwart drone pilot without whom none of this would have been possible. HKM was supported by National Aeronautics and Space Administration (NASA) Future Investigators in NASA Earth and Space Science and Technology (FINESST) grant 80NSSC21K1598 and a California Institute of Technology Geological and Planetary Sciences Geology Option Postdoctoral position. DAE was supported by National Sciences Foundation grant EAR-2321056. QWL was supported by a University of Waterloo New Faculty Starter Grant. All authors were supported by the Environmental Resilience Institute, funded by Indiana University’s Prepared for Environmental Change Grand Challenge initiative.</p> <p> </p> <p>UPDATES: <br>- 2024-04-29: Added Supporting Tables S1-S6.<br>- 2024-05-04: Updated some column headers in Supporting Tables S1-S6.<br>- 2024-05-08: Made public, updated the first paragraph (including changing manuscript status to accepted), and added contact information for further inquiries.<br>- 2024-06-20: Added DOI link to published manuscript in JGR:ES. Added a reference to our ESPL paper for those interested in more methodology details. Expanded the description of how the data were collected and processed, as well as my contact information, to make the repository a bit more user-friendly.</p>
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.