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opencc-by-4.0Jul 2020View details →

Fig. 1 in Review Of The Helminths Parasitic In Rare Aquatic Birds In Ukraine

Fig. 1. Localities of the material collection: — based on collection and literature; — based on collection; — based on literature.

Fig. 2 in Rare Late Miocene Seal Taxa (Carnivora, Phocidae) From The North Sea Basin

Fig. 2. Platyphoca danica sp. n., holotype, distal part of left humerus. Skaerum MØlle, Jutland, Denmark, Gram Formation (late Miocene, early-middle Tortonian, 8.0–11.5 ma); GM1: 2A — caudal; 2B — cranial view. Рис. 2. Gryphoca danica sp. n., голотип, дистальная часть левой плечевой кости; Скерум-Мёлле, Ютландия, Дания; грамская свита (поздний миоцен, верхний-средний тортон, 8,0–11,5 млн лет назад); GM1: 2A — вид сзади; 2B — вид спереди.

Plate 2. Fig. 1 in Rare Late Miocene Seal Taxa (Carnivora, Phocidae) From The North Sea Basin

Plate 2. Fig. 1. Gryphoca similis, left humerus. Lee Creek Mine Yorktown Formation (Pliocene, 5.0–5.8 ma); аfter Koretsky, Ray (2008: fig. 16–18); USNM 263625: 1A— caudal; 1B — cranial; 1C — medial; 1D — lateral view. Рис. 1. Gryphoca similis, левая плечевая кость из Ли-Крик, формация Йорктаун (плиоцен, 5.0–5.8 млн лет назад); по: Koretsky, Ray (2008: рис. 16–18); USNM 263625: 1A — вид спереди; 1B — вид сзади; 1C — вид с медиальной стороны; 1D — вид с латеральной стороны.

Figs 6–14 in New And Rare Spider Species (Arachnida, Araneae) From Ukraine

Figs 6–14. Drassyllus crimeaensis: 6 — epigyne ventral; Zelotes erebeus: 7 — epigyne ventral; Micaria coarctata: 8 — carapace dorsal, male palp: 13 — ventral, 14 — retrolateral; Turkоzelotes kazachstanicus: male palp: 9 — ventral, 10 — retrolateral; Zelotes prishutovae male palp: 11 —ventral, 12 — retrolateral. Scale bars: fig. 8 — 1 mm; figs. 6–7, 9–14 — 0.1 mm.

Figs 31–34 in New And Rare Spider Species (Arachnida, Araneae) From Ukraine

Figs 31–34. Bassanioides caperatus: male palp: 31 — retrolateral, 32 — prolateral, 33 — ventral; Heriaeus horridus: 34 — general appearance dorsal. Scale bars 0.1 mm.

Figs 23–30 in New And Rare Spider Species (Arachnida, Araneae) From Ukraine

Figs 23–30. Alopecosa steppica: male palp: 23 — ventral; Xysticus mongolicus: 24 — general appearance dorsal (after Polchaninova 2013, drawing by V. Timokhanov); Bassanioides caperatus: male palp: 25 — ventral, 26 — retrolateral; Heriaeus horridus: male palp: 27 — ventral, 28 — retrolateral; Ozyptila tuberosa: male palp: 29 — ventral, 30 — retrolateral. Scale bars 0.1 mm.

Figs 1–5 in New And Rare Spider Species (Arachnida, Araneae) From Ukraine

Figs 1–5. Devade tenella: 1 — general appearance dorsal; Dictyna sinuata: male palp: 2 — ventral, 3 — ventralprolateral, 4 — prolateral, 5 — dorsal. Scale bars: fig. 1 — 1 mm; figs. 2–5 — 0.1 mm.

Figs 19–22 in New And Rare Spider Species (Arachnida, Araneae) From Ukraine

Figs 19–22. Alopecosa steppica: male palp: 19 — ventral, 20 — retrolateral; 21 — epigyne ventral, 22 — vulva. Scale bars 0.1 mm.

Figs 15–18 in New And Rare Spider Species (Arachnida, Araneae) From Ukraine

Figs 15–18. Zelotes pseudogallicus: male palp: 15 — ventral, 16 — retrolateral; 17 — epigyne ventral, 18 — vulva. Scale bars 0.1 mm.

opencc-by-4.0Apr 2022View details →

Data of publication A Frequency-Multiplexed Coherent Electro-optic Memory in Rare Earth Doped Nanoparticles

Data corresponding to main text figures of publication : A. Fossati, S. Liu, J. Karlsson, A. Ikesue, A. Tallaire, A. Ferrier, D. Serrano, and P. Goldner, A Frequency-Multiplexed Coherent Electro-Optic Memory in Rare Earth Doped Nanoparticles, Nano Lett. 20, 7087 (2020).

Plate 3. Fig. 1 in Rare Late Miocene Seal Taxa (Carnivora, Phocidae) From The North Sea Basin

Plate 3. Fig. 1. Platyphoca vulgaris, distal part of left humerus. Lee CreekMine, Yorktown Formation (Pliocene, 5.0– 5.8 ma); аfter Koretsky, Ray (2008: fig. 2 E–F); USNM 456523: 1A — caudal; 1B — cranial view. Рис. 1. Platyphoca vulgaris, дистальная часть левой плечевой кости; из Ли-Крик, формация Йорктаун (плиоцен, 5.0–5.8 млн лет назад); по: Koretsky, Ray (2008: рис. 2 E–F); USNM 456523: 1A — вид сзади; 1B — вид спереди.

Plate 1. Fig. 1 in Rare Late Miocene Seal Taxa (Carnivora, Phocidae) From The North Sea Basin

Plate 1. Fig. 1. Pontophoca sarmatica, right femur; Kishinev, Moldavia (Middle Miocene, middle Sarmatian); аfter Koretsky, Grigorescu (2002: fig. 3); USNM 214980: 1A — cranial; 1B — caudal view. Рис. 1. Pontophoca sarmatica, правая бедренная кость; Кишинев, Молдова (средний миоцен, средний сармат); по: Koretsky, Grigorescu (2002: рис. 3); USNM 214980: 1A — вид спереди; 1B — вид сзади.

Fig. 3 in Rare Late Miocene Seal Taxa (Carnivora, Phocidae) From The North Sea Basin

Fig. 3. Gryphoca nordica sp. n., paratype, proximal part of right humerus (reversed); Gram, Jutland, Denmark. Clay pit of Gram Teglvaerk, Gram Formation (late Miocene, early-middle Tortonian, 8.0–11.5 ma); MSM 1404x1 (cast in Geological Museum, Copenhagen, Denmark): 3A — caudal; 3B — cranial; 3C — medial; 3D — lateral view. Abbreviations: ac — anconeal crest; rf — radial fossa; sg — spiral groove. Рис. 3. Gryphoca nordica sp. n., паратип, проксимальная часть правой плечевой кости (перевернута); Грам, Ютландия, Дания; карьер Грамского кирпичного завода, грамская свита (поздний миоцен, верхний-средний тортон, 8,0–11,5 млн лет назад); MSM 1404x1 (копия из Геологического музея, Копенгаген, Дания): 3A — вид сзади; 3B — вид спереди; 3C — вид с медиальной стороны; 3D — вид с латеральной стороны. Сокращения: ac — локтевой гребень; rf — лучевая ямка; sg — спиральная борозда.

Fig. 2 in Rare Late Miocene Seal Taxa (Carnivora, Phocidae) From The North Sea Basin

Fig. 2. Pontophoca jutlandica sp. n., holotype, incomplete right femur; Gram, Jutland, Denmark. Clay pit of Gram Teglvaerk, Gram Formation (late Miocene, early-middle Tortonian, 8.0–11.5 ma); MSM 1788: 2A — cranial; 2B — caudal view. Рис. 2. Pontophoca jutlandica sp. n., голотип, неполная правая бедренная кость; Грам, Ютландия, Дания. Карьер Грамского кирпичного завода, грамская свита (поздний миоцен, верхний-средний тортон, 8,0–11,5 млн лет назад); MSM 1788: 1A — вид спереди; 1B — вид сзади.

opencc-by-4.0Apr 2022View details →

Data of paper Controlling the interfacial reactions and environment of rare-earth ions in thin oxide films towards wafer-scalable quantum technologies

Data of the figures in the paper : N. Harada, A. Tallaire, D. Serrano, A. Seyeux, P. Marcus, X. Portier, C. Labbé, P. Goldner, and A. Ferrier, Controlling the Interfacial Reactions and Environment of Rare-Earth Ions in Thin Oxide Films towards Wafer-Scalable Quantum Technologies, Mater. Adv. 3, 300 (2022). doi: 10.1039/D1MA00753J

opencc-by-4.0May 2022View details →

Ethiopia – Distribution of Mother-Tongues – a rare 1976 map uncovered

As part of our study on historical cartography and ethno-linguistic maps in the Horn of Africa and Western Tigray, we discovered the language map for this book, which contains significant information on the geographic region where the Tigrinya language is spoken: "Language in Ethiopia”, by M. L. Bender, J. D. Bowen, R. L. Cooper and C. A. Ferguson, published by Oxford University Press in 1976. With regard to Western Tigray, on the map, the Tigrinya-speaking area extends from the Sudanese border up to the Rift Valley escarpment at the east. Two major rivers cross the Tigrinya language area, the Mereb at north and the Tekeze in the southern part. The same language community lives on both sides of the rivers. In addition to Tigrinya, the map also shows that Kunama is spoken on the southern shores of the lower Tekeze River. The extent of the Tigrinya language on this map is in line with the Tigrinya-speaking area shown on all-but-one other language maps (often prepared by senior linguists), which are further detailed in a parallel dataset (Nyssen, J. 2022. Database: Western Tigray in 96 historical and ten ethno-linguistic maps (1607-2009): Zenodo. <a href="https://doi.org/10.5281/zenodo.6557918">https://doi.org/10.5281/zenodo.6557918)</a>.

opencc-by-4.0Jul 2022View details →

Systematic analysis of disease-linked rare germline variants reveals new classes of cancer predisposing genes

<ul> <li>GEMs_Liver-HCC: 312 cancer patient-specific genome-scale metabolic models (GEMs) for Liver-HCC reconstructed using the RNA-seq data from PCAWG-TCGA Liver-HCC samples and generic human GEM 'Recon 2M.2'</li> <li>GEMs_Lung-SCC: 493 cancer patient-specific GEMs for Lung-SCC reconstructed using the RNA-Seq data from PCAWG-TCGA Lung-SCC samples and generic human GEM 'Recon 2M.2'</li> </ul> All the patient-specific GEMs were generated using a previously developed method (i.e., tINIT algorithm with a rank-based weight function), which is available at <a href="https://bitbucket.org/kaistmbel/recon-manager">https://bitbucket.org/kaistmbel/recon-manager</a>.

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Data from: Diversity among rare and common congeneric plant species from the Garry oak and Okanagan shrub-steppe ecosystems in British Columbia: implications for conservation

Using universal non-coding chloroplast DNA markers (cpDNA), we investigated genetic diversity and genetic structure in four rare and common plant species pairs inhabiting threatened ecosystems (Garry Oak and Okanagan shrub-steppe) in British Columbia. The species found in the Garry oak ecosystem are: Sanicula bipinnatifida (purple sanicle; Apiaceae; rare), Sanicula crassicaulis (Pacific sanicle; Apiaceae; common), and Balsamorhiza deltoidea (deltoid balsamroot; Asteraceae; rare). The species found in the Okanagan shrub-steppe ecosystem are: Balsamorhiza sagittata (arrowleaf balsamroot; Asteraceae; common), Orthocarpus barbatus (Grand Coulee owl-clover; Orobanchaceae; rare), Orthocarpus luteus (yellow owl-clover; Orobanchaceae; common), Phacelia ramosissima (branching phacelia; Hydrophyllaceae; rare), and Phacelia linearis (thread-leaved phacelia; Hydrophyllaceae; common). Eight cpDNA regions were sequenced for each study species. Sequences were aligned and concatenated within each species, and single nucleotide polymorphisms (SNPs) were used to analyze patterns of regional genetic diversity and phylogeographic structure within genera and species. Results include: total gene diversity (Ht), nucleotide diversity (π), number of private alleles, haplotype networks, isolation by distance, and analysis of molecular variance.

opencc-zeroJul 2022View details →

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Rare and declining bee species are key to consistent pollination of wildflowers and crops across large spatial scales

Biodiversity promotes ecosystem function in experiments, but it remains uncertain how biodiversity loss affects function in larger-scale natural ecosystems, where rare and declining species which are likely to be lost and function needs to be maintained across space and time. Here we explore the importance of rare and declining bee species to the pollination of three wildflowers and three crops using large-scale (72 sites across 5,000 km2), multi-year datasets. Half (82/164) bee species were rare or declining, but these species provided ~15% of overall pollination. To determine the number of species important to ecosystem function, we used two methods of 'scaling up', both of which have previously been used for biodiversity-function analysis. First, we summed bee species' contributions to pollination across space and time and then found the minimum set of species needed to provide a threshold level of function across all sites; according to this method, effectively no rare and declining bee species were important to pollination. Second, we account for the "insurance value" of biodiversity by finding the minimum set of bee species needed to simultaneously provide a threshold level of function at each site in each year. The second method leads to the conclusion that 25 rare and eight declining bee species (36% and 53% of all rare and declining bee species, respectively) are important. Our findings provide some of the strongest evidence yet for the importance of rare and declining species, thereby providing a more direct link between real-world biodiversity loss and ecosystem function.

opencc-zeroJul 2022View details →