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Figure 9 in Notes on a recently described subspecies, and the poorly known nominate subspecies of Rüppell's Parrot, Poicephalus rueppellii mariettae and P. r. rueppellii
Figure 9. Three of the four specimens received alive at London Zoo in April 1882 and which died in June 1882, from left to right: male, NHMUK 1890.4.1.19; male, NHMUK 1890.4.1.20; female, NHMUK 1890.4.1.21 (Jonathan Jackson, © Natural History Museum, London)
Figure 8 in Notes on a recently described subspecies, and the poorly known nominate subspecies of Rüppell's Parrot, Poicephalus rueppellii mariettae and P. r. rueppellii
Figure 8. Bird specimens collected by C. J. Andersson in 1850 in Damaraland (Namibia) were sold by the dealer A. D Bartlett of London and some were acquired by the British Museum, including this male (NHMUK 1852.5.1.15), on left in A and B, and female (NHMUK 1852.5.1.16) Rüppell's Parrot Poicephalus rueppellii mariettae. These specimens were seen by Strickland & Sclater (1852) and, because Andersson had not sexed the birds during preparation, due to the differences in colour it was assumed that the more colourful individual was the male (Jonathan Jackson, © Natural History Museum, London)
Figure 5 in Notes on a recently described subspecies, and the poorly known nominate subspecies of Rüppell's Parrot, Poicephalus rueppellii mariettae and P. r. rueppellii
Figure 5. Specimen of nominate Rüppell's Parrot Poicephalus rueppellii from north Angola, in the Naturalis Biodiversity Center, RMNH.AVES.209654, which is smaller and overall darker but has the blue rump and belly paler than birds from south-west Angola and Namibia (© Naturalis Biodiversity Center, Leiden)
Figure 4 in Notes on a recently described subspecies, and the poorly known nominate subspecies of Rüppell's Parrot, Poicephalus rueppellii mariettae and P. r. rueppellii
Figure 4. Female of the recently described Poicephalus rueppellii mariettae, Namibia, 4 March 2018; this taxon, with dark ultramarine-blue plumage in females, is better known and more widespread than the nominate subspecies (© Charles James Sharp)
Фототаблица 2 Plate 2 A, B – Crassostrea gigas (Thunberg, 1793): СевернаЯ КореЯ, провинциЯ Северный Хамгён, высота 91.3 мм, ЗМ ДВФУ № 38379/Bv-5785; C, D – Pododesmus (Monia) macrochisma (Deshayes, 1839): СевернаЯ КореЯ, провинциЯ Северный Хамгён, Чипсам, длина 49.6 мм, ЗМ ДВФУ № 38635/Bv-5915; E, F – Mactra (Mactra) chinensis Philippi, 1846: СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 47.5 мм, ЗМ ДВФУ № 38353/Bv-5769; G, H – Spisula (Pseudocardium) sachalinensis (Schrenck, 1861): СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 95.0 мм, ЗМ ДВФУ № 38355/Bv-5771; I, J – Mactromeris polynyma (Stimpson, 1860): СевернаЯ КореЯ, провинциЯ Северный Хамгён, Чипсам, длина 45.6 мм, ЗМ ДВФУ № 38625/Bv-5905; K–N – Mizuhopecten yessoensis (Jay, 1857): СевернаЯ КореЯ, провинциЯ Северный Хамгён, г. ЧхондЖин, рынок, длина 65.9 мм, ЗМ ДВФУ № 38377/Bv-5783; O–P – Chlamys (Swiftopecten) swiftii (Bernardi, 1858): СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 70.8 мм, ЗМ ДВФУ № 38378/Bv-5784. A, B – Crassostrea gigas (Thunberg, 1793): North Korea, North Hamgyong Province, shell height 91.3 mm, ZMFU no. 38379/Bv-5785; C, D – Pododesmus (Monia) macrochisma (Deshayes, 1839): North Korea, North Hamgyong Province, Jipsam, shell length 49.6 mm, ZMFU no. 38635/Bv-5915; E, F – Mactra (Mactra) chinensis Philippi, 1846: North Korea, North Hamgyong Province, shell length 47.5 mm, ZMFU no. 38353/Bv-5769; G, H – Spisula (Pseudocardium) sachalinensis (Schrenck, 1861): North Korea, North Hamgyong Province, shell length 95.0 mm, ZMFU no. 38355/Bv-5771; I, J – Mactromeris polynyma (Stimpson, 1860): North Korea, North Hamgyong Province, Jipsam, shell length 45.6 mm, ZMFU no. 38625/Bv-5905; K–N – Mizuhopecten yessoensis (Jay, 1857): North Korea, North Hamgyong Province, Chongjin City, market, shell length 65.9 mm, ZMFU no. 38377/Bv-5783; O–P – Chlamys (Swiftopecten) swiftii (Bernardi, 1858): North Korea, North Hamgyong Province, shell length 70.8 mm, ZMFU no. 38378/Bv-5784. in On the bivalve molluscan fauna of North Hamgyong Province (North Korea)
Фототаблица 2 Plate 2 A, B – Crassostrea gigas (Thunberg, 1793): СевернаЯ КореЯ, провинциЯ Северный Хамгён, высота 91.3 мм, ЗМ ДВФУ № 38379/Bv-5785; C, D – Pododesmus (Monia) macrochisma (Deshayes, 1839): СевернаЯ КореЯ, провинциЯ Северный Хамгён, Чипсам, длина 49.6 мм, ЗМ ДВФУ № 38635/Bv-5915; E, F – Mactra (Mactra) chinensis Philippi, 1846: СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 47.5 мм, ЗМ ДВФУ № 38353/Bv-5769; G, H – Spisula (Pseudocardium) sachalinensis (Schrenck, 1861): СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 95.0 мм, ЗМ ДВФУ № 38355/Bv-5771; I, J – Mactromeris polynyma (Stimpson, 1860): СевернаЯ КореЯ, провинциЯ Северный Хамгён, Чипсам, длина 45.6 мм, ЗМ ДВФУ № 38625/Bv-5905; K–N – Mizuhopecten yessoensis (Jay, 1857): СевернаЯ КореЯ, провинциЯ Северный Хамгён, г. ЧхондЖин, рынок, длина 65.9 мм, ЗМ ДВФУ № 38377/Bv-5783; O–P – Chlamys (Swiftopecten) swiftii (Bernardi, 1858): СевернаЯ КореЯ, провинциЯ Северный Хамгён, длина 70.8 мм, ЗМ ДВФУ № 38378/Bv-5784. A, B – Crassostrea gigas (Thunberg, 1793): North Korea, North Hamgyong Province, shell height 91.3 mm, ZMFU no. 38379/Bv-5785; C, D – Pododesmus (Monia) macrochisma (Deshayes, 1839): North Korea, North Hamgyong Province, Jipsam, shell length 49.6 mm, ZMFU no. 38635/Bv-5915; E, F – Mactra (Mactra) chinensis Philippi, 1846: North Korea, North Hamgyong Province, shell length 47.5 mm, ZMFU no. 38353/Bv-5769; G, H – Spisula (Pseudocardium) sachalinensis (Schrenck, 1861): North Korea, North Hamgyong Province, shell length 95.0 mm, ZMFU no. 38355/Bv-5771; I, J – Mactromeris polynyma (Stimpson, 1860): North Korea, North Hamgyong Province, Jipsam, shell length 45.6 mm, ZMFU no. 38625/Bv-5905; K–N – Mizuhopecten yessoensis (Jay, 1857): North Korea, North Hamgyong Province, Chongjin City, market, shell length 65.9 mm, ZMFU no. 38377/Bv-5783; O–P – Chlamys (Swiftopecten) swiftii (Bernardi, 1858): North Korea, North Hamgyong Province, shell length 70.8 mm, ZMFU no. 38378/Bv-5784.
Figure 5 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 5. Persian Shearwater Puffinus persicus persicus, off Watamu, coastal Kenya, 1 March 2022, showing the characteristic brown-toned upperparts, much-reduced white in the underwing-coverts, dusky axillaries and brown flanks streaking of this taxon (Jaap Gijsbertsen)
Figure 4 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 4. Persian Shearwater Puffinus persicus, ashore near Pangani, north-east Tanzania, 14 March 2009, showing the characteristic dusky underwing, axillaries, and faint white spot in front of the eye (© B. Simonsen)
Figure 1 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 1. Specimens of Persian Shearwater Puffinus persicus persicus (A) NMK 1442019 (Sidney Shema), (B) NMK B9189 (Sidney Shema), (C) NMK B8032 (Sidney Shema) and Tropical Shearwater Puffinus bailloni nicolae (D) AMNH 788928 (© Augie Kramer) collected in Kenya between 1963 and 2019, alongside a paratype of P. b. nicolae (E) MNHN-ZO-MO-1878-1051 (www.science.mnhn.fr/institution/mnhn/collection/zo/item/ search?lang=en_US) from the Seychelles. Birds not to scale.
Figure 3 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 3. Persian Shearwater Puffinus persicus persicus, Diani, coastal Kenya, 26 February 2019, before it died (© S. Kapila)
Figure 1 in Notes on a recently described subspecies, and the poorly known nominate subspecies of Rüppell's Parrot, Poicephalus rueppellii mariettae and P. r. rueppellii
Figure 1. Distribution map of Rüppell's Parrot Poicephalus rueppellii based on e-Bird (https://ebird. org/species/ruepar1?siteLanguage=de). P. r. rueppellii (red dots) occurs only in north-west and west-central Angola around Luanda and Benguela, whereas P. r. mariettae (green dots) is widespread in Namibia and south-west Angola (© Thomas Arndt)
Figure 2 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 2. Persian Shearwater Puffinus persicus persicus off Oman (left ML 155569281; © Marcel Gil Velasco) and United Arab Emirates (right ML 93690941; © Tommy Pedersen) alongside the December 1981 specimen from Mtwapa Creek, Kenya (centre NMK B9189; Sidney Shema), showing typical pattern of wear and fading on head producing white grizzling / streaking, and a poorly demarcated border between cheeks and throat.
Fig. 3 in Phyllanthus novofriburgensis and P. pedrosae, two new species of Phyllanthus subsect. Clausseniani (Phyllanthaceae) from Southeastern Brazil
Fig. 3. Distribution map of Phyllanthus novofriburgensis J.C.R.Mendes, J.M.A.Braga & Fraga sp. nov. (white square) and P. pedrosae J.C.R.Mendes, J.M.A.Braga & Fraga sp. nov. (white circle). State abbreviations: ES = Espírito Santo; MG = Minas Gerais; RJ = Rio de Janeiro; SP = São Paulo.
Fig. 4. Phyllanthus pedrosae J.C.R.Mendes, J.M.A in Phyllanthus novofriburgensis and P. pedrosae, two new species of Phyllanthus subsect. Clausseniani (Phyllanthaceae) from Southeastern Brazil
Fig. 4. Phyllanthus pedrosae J.C.R.Mendes, J.M.A.Braga & Fraga sp. nov. A‒B. Habitat. C. Branches (in detail the shape of the branches, as well as the apex of the leaf blade). D. Floral branches. E. Branches with a staminate flower in detail. F‒G. Capsule. Photos by J.C.R. Mendes (A–B), L. Pedrosa (C–E) and F–G by M.C.T.B. Messias (OUPR [6395]).
Fig. 1. A‒F. Phyllanthus novofriburgensis J.C.R.Mendes, J.M.A in Phyllanthus novofriburgensis and P. pedrosae, two new species of Phyllanthus subsect. Clausseniani (Phyllanthaceae) from Southeastern Brazil
Fig. 1. A‒F. Phyllanthus novofriburgensis J.C.R.Mendes, J.M.A.Braga & Fraga sp. nov. A. Branches. B. Leaf blade. C. Cymule. D. Staminate flower. E. Pistillate flower. F. Capsule. G‒M. Phyllanthus pedrosae J.C.R.Mendes, J.M.A.Braga & Fraga sp. nov. G. Branches. H. Branch detail [angular]. I. Leaf blade [in detail the mucronate apex]. J. Staminate flower. K. Pistillate flower. L. Capsule. M. Seed. Illustration designs based on type specimens by Regina Carvalho.
Figure 1 in Detection of the Trp-2027-Cys Mutation in Fluazifop-P-butyl-resistant Itchgrass (RottboelliO cochinchinensis) using High-Resolution Melting Analysis (HRMA)
Figure 1. Sequence alignment showing the single-nucleotide change (G/C) within the chloroplastic acetyl-coenzyme A carboxylase gene carboxyl-transferase domain fragments from Rottboellia cochinchinensis susceptible (G) and resistant (C) biotypes. The sequences of the HRMA primers are colored in red. Position numbers (Alopecurus myosuroides full ACCase sequence, GenBank AJ310767, numbering) are given above the nucleotide sequences. Conserved nucleotides are indicated by dots.
FIG. 1 in The Raymond Benoist microslide library of woods of French Guiana at the Herbarium of Paris (P): restoration and comments
FIG. 1. — Raymond Benoist (1881-1970): A, portrait of c. 1930, Muséum national d'Histoire naturelle ©; B, a tray with the arrangement of slides of wood until 2021.
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats.
SI Figure 1: Dispersion values (a boxplot using distance to centroids based on Bray Curtis distance matrix) of external and internal bacterial microbiome composition for different hosts. In a mixed linear model, microinvertebrates did not significantly impact dispersion (P=0.44), but microbiome type did (P=0.03). Pairwise contrasts show that while external microbiomes of P. murrayi and Tardigrada are more variable than their internal microbiomes, E. antarcticus external and internal microbiomes are equally variable. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 1: Dispersion values (a boxplot using distance to centroids based on Bray Curtis distance matrix) of external and internal bacterial microbiome composition for different hosts. In a mixed linear model, microinvertebrates did not significantly impact dispersion (P=0.44), but microbiome type did (P=0.03). Pairwise contrasts show that while external microbiomes of P. murrayi and Tardigrada are more variable than their internal microbiomes, E. antarcticus external and internal microbiomes are equally variable.
Supplementary material from: Wolz D, Seidel-Greiff R, Behnisch T, Kruppke I, Kuznik I, Bertram P, Jäger H, Gude M, Cherif C (2024) Potentials of Polyacrylonitrile Substitution by Lignin for Continuous Manufactured Lignin/Polyacrylonitrile-Blend-Based Carbon Fibers
<p>This material contains all research data concerning the analyses conducted in the work taht was published as "<strong>Potentials of Polyacrylonitrile Substitution by Lignin for Continuous Manufactured Lignin/Polyacrylonitrile-Blend-Based Carbon Fibers</strong>" in the <strong>MDPI</strong> journal <strong>Fibers.</strong></p> <p>Process data cannot be included for reasons of confidentiality.</p>
Fig. 15. The track Amphisauropus Haubold, 1970, NMMNH P-37922 in Evolution and identity of synapsid carpal bones
Fig. 15. The track Amphisauropus Haubold, 1970, NMMNH P-37922, central New Mexico, USA, Abo Formation, Cisuralian, left manus and pes imprint, convex hyporelief, presumably from a seymouriamorph trackmaker. Photo made by Sebastian Voigt, published with the permission of Sebastian Voigt, all rights reserved (see also Voigt and Lucas 2017: fig. 3F).
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.