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324 results for “arabica”
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V. v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V. v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).
Genetic composition and diversity of Arabica coffee in the crop's center of origin and its impact on four major fungal diseases
<p><span>Conventional wisdom states that </span><span>genetic variation reduces disease levels in plant populations. Nevertheless, crop species have been subject to a gradual loss of genetic variation through selection for specific traits during breeding, thereby increasing their vulnerability to biotic stresses such as pathogens. We explored how genetic variation in Arabica coffee sites in southwestern Ethiopia was related to the incidence of four major fungal diseases. Sixty sites were selected along a gradient of management intensity, ranging from nearly wild to intensively managed coffee stands. We used genotyping-by-sequencing of pooled leaf samples (pool-GBS) derived from 16 individual coffee shrubs in each of the sixty sites to assess the variation in genetic composition (multivariate: reference allele frequency) and genetic diversity (univariate: mean expected heterozygosity) between sites. </span><span>We found that genetic composition had a clear spatial pattern and that genetic diversity was higher in less managed sites</span><span>. The incidence of the four fungal diseases was related to the genetic composition of the coffee stands, but in a specific way for each disease. In contrast, genetic diversity was only related to the within-site variation of coffee berry disease, but not to the mean incidence of any of the four diseases across sites. Given that fungal diseases are major challenges of Arabica coffee in its native range, our findings that genetic composition of coffee sites impacted the major fungal diseases may serve as baseline information to study the molecular basis of disease resistance in coffee. </span><span>Overall, our study illustrates the need to consider both host genetic composition and genetic diversity when investigating the genetic basis for variation in disease levels</span><span>. </span></p>
FIGURE 2 in Crassiparies yunnanensis sp. nov. (Neohendersoniaceae, Pleosporales) from dead twigs of Coffea arabica in China
FIGURE 2. Crassiparies yunnanensis (HKAS 121977, holotype). a, b. Ascomata on coffee twig surface (arrow indicates orange secretion). c, d. Vertical section of ascomata. e. Peridium. f. Hamathecium. g–k. Asci. l–q. Ascospores. r. Germinating ascospore. s. Colony on PDA medium. Scale bars: c = 100 µm, d = 50 µm, e, r = 20 µm, f = 50 µm, g–k = 30 µm, l–q = 10 µm.
FIGURE 1 in Crassiparies yunnanensis sp. nov. (Neohendersoniaceae, Pleosporales) from dead twigs of Coffea arabica in China
FIGURE 1. RAxML tree based on a combined dataset of SSU, LSU, ITS, rpb2, and tef genes sequences. Bootstrap support values for ML equal to or greater than 75% and BYPP equal to or greater than 0.95 are given above the nodes. Strains of the newly described species are in red, while type strains are in bold.
FIGURE 3 in Crassiparies yunnanensis sp. nov. (Neohendersoniaceae, Pleosporales) from dead twigs of Coffea arabica in China
FIGURE 3. Crassiparies yunnanensis (KUMCC 21-0215, ex-type) on PDA. a. Germinating ascospore. b, c. Growth of asexual morph on plant tissues on PDA. d–g. Chlamydospores growing from hyphae. h. Chlamydospores. Scale bars: a, d–h = 20 µm.
On following pages: 189. Isfahan Sheep (Ovis isphahanica); 190. Laristan Sheep (Ovis laristanica); 191. Ladakh Urial (Ovis vignei); 192. Punjab Urial (Ovis punjabiensis); 193. Bukhara Urial (Ovis bochariensis); 194. Arabian Wild Sheep (Ovis arabica); 195. Afghan Urial (Ovis cycloceros). in Bovidae
On following pages: 189. Isfahan Sheep (Ovis isphahanica); 190. Laristan Sheep (Ovis laristanica); 191. Ladakh Urial (Ovis vignei); 192. Punjab Urial (Ovis punjabiensis); 193. Bukhara Urial (Ovis bochariensis); 194. Arabian Wild Sheep (Ovis arabica); 195. Afghan Urial (Ovis cycloceros).
FIGURE 9. Echinolittorina arabica. A–G, penes. H, I, pallial oviducts. J, K, paraspermatozoa. A in The genus Echinolittorina Habe, 1956 (Gastropoda: Littorinidae) in the Indo-West Pacific Ocean
FIGURE 9. Echinolittorina arabica. A–G, penes. H, I, pallial oviducts. J, K, paraspermatozoa. A, Kuwait (BMNH 20030878; shell H = 7.8 mm). B–D, J, K, Dubai, United Arab Emirates (BMNH 20030879; shell H B = 6.6 mm, C = 7.0 mm, D = 7.3 mm). E, Ghemeis Peninsula, Abu Dhabi, United Arab Emirates (BMNH 20030880; shell H = 7.6 mm). F, Fujaira, United Arab Emirates (BMNH 20030881; shell H = 7.7 mm). G, Ras al-Khaimah Khor, United Arab Emirates (BMNH 20030875; shell H = 8.4 mm). H, Hamriya, Sharjah, United Arab Emirates (BMNH 20030871; shell H = 7.7 mm). I, Al Bustan, Muscat, Oman (ZMA; shell H = 9.2 mm). Shading conventions as in Figure 3.
On following pages: 270. Cranbrook's White-toothed Shrew (Crocidura cranbrooki); 271. Hill's White-toothed Shrew (Crocidura hilliana); 272. Voracious White-toothed Shrew (Crocidura vorax); 273. Sa Pa White-toothed Shrew (Crocidura sapaensis); 274. Annamite White-toothed Shrew (Crocidura annamitensis); 275. Vietnamese White-toothed Shrew (Crocidura guy); 276. Ke Go White-toothed Shrew (Crocidura kegoensis); 277. Andaman Spiny White-toothed Shrew (Crocidura hispida); 278. Andaman White-toothed Shrew (Crocidura andamanensis); 279. Jenkins's White-toothed Shrew (Crocidura jenkinsi); 280. Nicobar White-toothed Shrew (Crocidura nicobarica); 281. Christmas Island White-toothed Shrew (Crocidura trichura): 282. Siberian White-toothed Shrew (Crocidura sibirica); 283. Shantung White-toothed Shrew (Crocidura shantungensis); 284. Glldenstadt's White-toothed Shrew (Crocidura gueldenstaedtii); 285. Lesser White-toothed Shrew (Crocidura suaveolens); 286. Cyrenaica White-toothed Shrew (Crocidura aleksandrisi); 287. Zarudny's White-toothed Shrew (Crocidura zarudnyi); 288. Greater Ryukyu White-toothed Shrew (Crocidura orii); 289. Batak White-toothed Shrew (Crocidura batakorum); 290. Mossy Forest White-toothed Shrew (Crocidura musseril); 291. Temboan White-toothed Shrew (Crocidura rhoditis); 292. Lesser Black-footed White-toothed Shrew (Crocidura lea): 293. Sulawesi Tiny White-toothed Shrew (Crocidura levicula); 294. Elongated White-toothed Shrew (Crocidura elongata); 295. North African White-toothed Shrew (Crocidura pachyura); 296. Greater White-toothed Shrew (Crocidura russula); 297. Serezkaya White-toothed Shrew (Crocidura serezkyensis); 298. Whitaker's White-toothed Shrew (Crocidura whitakeri); 299. Flower's White-toothed Shrew (Crocidura floweri): 300. Egyptian Pygmy White-toothed Shrew (Crocidurareligiosa); 301. Bicolored White-toothed Shrew (Crocidura leucodon); 302. Saharan White-toothed Shrew (Crocidura tarfayensis); 303. Arabian White-toothed Shrew (Crocidura arabica); 304. Dhofar White-toothed Shrew (Crocidura dhofarensis). in Soricidae
On following pages: 270. Cranbrook's White-toothed Shrew (Crocidura cranbrooki); 271. Hill's White-toothed Shrew (Crocidura hilliana); 272. Voracious White-toothed Shrew (Crocidura vorax); 273. Sa Pa White-toothed Shrew (Crocidura sapaensis); 274. Annamite White-toothed Shrew (Crocidura annamitensis); 275. Vietnamese White-toothed Shrew (Crocidura guy); 276. Ke Go White-toothed Shrew (Crocidura kegoensis); 277. Andaman Spiny White-toothed Shrew (Crocidura hispida); 278. Andaman White-toothed Shrew (Crocidura andamanensis); 279. Jenkins's White-toothed Shrew (Crocidura jenkinsi); 280. Nicobar White-toothed Shrew (Crocidura nicobarica); 281. Christmas Island White-toothed Shrew (Crocidura trichura): 282. Siberian White-toothed Shrew (Crocidura sibirica); 283. Shantung White-toothed Shrew (Crocidura shantungensis); 284. Glldenstadt's White-toothed Shrew (Crocidura gueldenstaedtii); 285. Lesser White-toothed Shrew (Crocidura suaveolens); 286. Cyrenaica White-toothed Shrew (Crocidura aleksandrisi); 287. Zarudny's White-toothed Shrew (Crocidura zarudnyi); 288. Greater Ryukyu White-toothed Shrew (Crocidura orii); 289. Batak White-toothed Shrew (Crocidura batakorum); 290. Mossy Forest White-toothed Shrew (Crocidura musseril); 291. Temboan White-toothed Shrew (Crocidura rhoditis); 292. Lesser Black-footed White-toothed Shrew (Crocidura lea): 293. Sulawesi Tiny White-toothed Shrew (Crocidura levicula); 294. Elongated White-toothed Shrew (Crocidura elongata); 295. North African White-toothed Shrew (Crocidura pachyura); 296. Greater White-toothed Shrew (Crocidura russula); 297. Serezkaya White-toothed Shrew (Crocidura serezkyensis); 298. Whitaker's White-toothed Shrew (Crocidura whitakeri); 299. Flower's White-toothed Shrew (Crocidura floweri): 300. Egyptian Pygmy White-toothed Shrew (Crocidurareligiosa); 301. Bicolored White-toothed Shrew (Crocidura leucodon); 302. Saharan White-toothed Shrew (Crocidura tarfayensis); 303. Arabian White-toothed Shrew (Crocidura arabica); 304. Dhofar White-toothed Shrew (Crocidura dhofarensis).
Cultivating Flavor: Unveiling the Impact of Lactobacillus Delbrueckii Subsp. Bulgaricus and Bean Sprouts (Phaseolus Vulgarison) on Fermentation Arabica and Robusta Coffee
<p>This material has presented on 2nd International Conference on Advance Research in Agriculture and Food 2023 in October 25, 2023.</p>
FIGURE 3. Indopinnixa arabica n in Two new species and a new record of infaunal crabs (Decapoda: Brachyura: Pinnotheridae and Varunidae) from Oman and Saudi Arabia
FIGURE 3. Indopinnixa arabica n. sp., holotype, male (6.7/3.2), Sur, Oman, FLMNH UF 65451, crab alive in different views: A, dorsal; B, ventral; C, anterodorsal; D, anterior (frontal). Photographs by A. Anker.
FIGURE 1. Indopinnixa arabica n in Two new species and a new record of infaunal crabs (Decapoda: Brachyura: Pinnotheridae and Varunidae) from Oman and Saudi Arabia
FIGURE 1. Indopinnixa arabica n. sp., holotype, male (6.7/3.2), Sur, Oman, FLMNH UF 65451: A, habitus, dorsal; B, anterior surface of carapace, buccal frame and chelipeds, anterior (frontal); C, sternum, pleon and telson, ventral; D, right chela, outer; E, left chela, outer. Photographs by R. Lasley.
Figure 2 in Genetic diversity of Arabica coffee (Coffea arabica L.) collections
Figure 2. Dendrogram obtained by Ward's minimum variance among Arabica coffee collections based on 32 SSR markers (green colour = Ethiopian Arabica coffee, and red colour = cultivated varieties).
FIGURE 4 in Hydnora arabica (Aristolochiaceae), a new species from the Arabian Peninsula and a key to Hydnora
FIGURE 4. Comparison of tepal margin setae of H. arabica and H. abyssinica. A) Dense strigose tepal margin setae from H. arabica (J. Bolin, S. Al Rahbi, L. Musselman, JFB2014OM3); the next panels show H. abyssinica with some variation in the tepal margin setae considered diffuse with with remote apices, B) H. abyssinica (BolinJB_09_8, WIND) C) H. abyssinica. (Musselman 6279a, US D) H. abyssinica (Luke 7182, US). (Size Bars = 1 mm)
FIGURE 1 in Hydnora arabica (Aristolochiaceae), a new species from the Arabian Peninsula and a key to Hydnora
FIGURE 1: Distribution of Hydnora arabica and Hydnora abyssinica in the Arabian Peninsula. A single collection of Hydnora abyssinica (Collenette 5119, K, RGBE), represented by a black circle (•) is reported from southwestern Saudi Arabia, approximate location. For Hydnora arabica open circles (O) are approximate locations from the literature and from herbarium labels without precise locality information. Black triangles (▲) represent collections conducted by the authors during Dec. 2014 based on GPS coordinate information. The recent Hydnora arabica collections with color photographs have been reported from Abaya Province, Yemen, grey shaded area (AlFatimi et al. 2015).
Figure 6 in The family Leucospidae (Hymenoptera: Chalcidoidea) from the South of Saudi Arabia, with the first report of the genus Micrapion and description of Leucospis arabica sp. nov.
Figure 6. Leucospis arabica sp. nov., paratype (male). (a) Habitus, lateral view; (b,c) head, frontal view; (d) head and mesosoma, dorsal view.
Figure 3 in The family Leucospidae (Hymenoptera: Chalcidoidea) from the South of Saudi Arabia, with the first report of the genus Micrapion and description of Leucospis arabica sp. nov.
Figure 3. Leucospis arabica sp. nov., holotype (female). (a,b) Habitus, in dorsal and lateral view, respectively (GT6 indicated by arrow); (c) antenna.
Figure 2 in The family Leucospidae (Hymenoptera: Chalcidoidea) from the South of Saudi Arabia, with the first report of the genus Micrapion and description of Leucospis arabica sp. nov.
Figure 2. Leucospis africana Cameron (male). (a) Head, frontal view; (b) mesoscutellum, postscutellum and propodeum, dorsal view (bidentate carina on postscutellum indicated by arrow); (c) gaster, lateral view, with hind coxa, femur and tibia (GT2 indicated by arrow).
Figure 8 in The family Leucospidae (Hymenoptera: Chalcidoidea) from the South of Saudi Arabia, with the first report of the genus Micrapion and description of Leucospis arabica sp. nov.
Figure 8. Leucospis elegans (female). (a) Habitus, dorso-lateral view; (b) head, antennae and pronotum, dorso-lateral view; (c) hind femur and tibia.
Figure 5 in The family Leucospidae (Hymenoptera: Chalcidoidea) from the South of Saudi Arabia, with the first report of the genus Micrapion and description of Leucospis arabica sp. nov.
Figure 5. Leucospis arabica sp. nov., holotype (female). (a) Mesoscutellum, postscutellum and propodeum, dorsal view (curved carina on postscutellum indicated by arrow); (b) hind coxa (serrate dorsal edge indicated by arrow); (c) gaster, dorsal view.
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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)
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.