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Radiocarbon dates of planktonic foraminifera in sediment core GeoB7702-3 ...

by Meyer, Vera D, Pätzold, Jürgen, Mollenhauer, Gesine, Castañeda, Isla S, Schouten, Stefan, Schefuß, Enno
Published 2024

Map Of The North Polar Region. The Graphic Co. 39 & 41 Park Place, N.Y. Wm. Bauman del. (inset profile) Wrangell Land . As seen from Bark Nile of New London, Capt. Th. Long. Aug. 14th, 15th & 16th 1867...

by Bauman, William
Published 1880

Map Of The North Polar Region. The Graphic Co. 39 & 41 Park Place, N.Y. Wm. Bauman del. (inset profile) Wrangell Land . As seen from Bark Nile of New London, Capt. Th. Long. Aug. 14th, 15th & 16th 1867...

by Bauman, William
Published 1880

Pilgrimages

by Viaud, Gérard
Published 1991

Correction: Predictive markers for the early prognosis of dengue severity: A systematic review and meta-analysis.

by Tran Quang Thach, Heba Gamal Eisa, AlMotsim Ben Hmeda, Hazem Faraj, Tieu Minh Thuan, Manal Mahmoud Abdelrahman, Mario Gerges Awadallah, Nam Xuan Ha, Michael Noeske, Jeza Muhamad Abdul Aziz, Nguyen Hai Nam, Mohamed El Nile, Shyam Prakash Dumre, Nguyen Tien Huy, Kenji Hirayama
Published in PLOS Neglected Tropical Diseases (2022)

Predictive markers for the early prognosis of dengue severity: A systematic review and meta-analysis.

by Tran Quang Thach, Heba Gamal Eisa, AlMotsim Ben Hmeda, Hazem Faraj, Tieu Minh Thuan, Manal Mahmoud Abdelrahman, Mario Gerges Awadallah, Nam Xuan Ha, Michael Noeske, Jeza Muhamad Abdul Aziz, Nguyen Hai Nam, Mohamed El Nile, Shyam Prakash Dumre, Nguyen Tien Huy, Kenji Hirayama
Published in PLOS Neglected Tropical Diseases (2021)

Martyrs, Coptic

by Atiya, Aziz Suryal, 1898-1988;
Published 1991

Province, Total Petroleum System and Assessment Unit Boundaries from the 2009-2011 World Petroleum Resources Project

by U.S. Geological Survey, World Conventional Resource Assessment Team
Published 2013

Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following...

by Wilson, Don E., Mittermeier, Russell A.
Published 2011

Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following...

by Wilson, Don E., Mittermeier, Russell A.
Published 2011

Pharaonic Egypt and the origins of plague

by Panagiotakopulu, Eva
Published in Journal of Biogeography (2004)

Nd isotope data for planktonic foraminifera from within and around sapropels S1 and S5 from ODP Site 160-967

by Scrivner, Adam E, Vance, Derek, Rohling, Eelco J
Published 2004

Holocene aridity-induced interruptions of human activity along a fluvial channel in Egypt's northern delta

by Stanley, Jean-Daniel, Ullmann, Tobias, Lange-Athinodorou, Eva
Published in Quaternary (2021)

Thirteen thousand years of southeastern Mediterranean climate variability inferred from an integrative planktic foraminiferal-based approach

by M. Mojtahid, R. Manceau, R. Schiebel, R. Hennekam, G.J. De Lange
Published in Paleoceanography (2015)

Stable isotope analysis on planktic foraminifera in sediment cores from the eastern Mediterranean sapropel formation

by Jenkins, Janice A, Williams, Douglas F
Published 1984

Canadian Cooperative Wildlife Health Centre, Volume 9-2, Fall 2003

Published 2003

Mechanism and Conditions of Failure of a Gigantic Mass Wasting Event in Basalt: A Geotechnical Investigation of the Sanford Pasture Landslide Complex, Yakima County, Washington

by Keffeler, Evan
Published 2018

Use of staphylococcal protein A in the analysis of teleost immunoglobulin structural diversity

by Bromage, Erin S., Ye, Jianmin, Owens, Leigh, Kaattari, Ilsa M., Kaattari, Stephen L.
Published in Developmental & Comparative Immunology (2004)

ISIMIP2a Simulation Data from Water (regional) Sector

by Krysanova, Valentina, Hattermann, Fred, Aich, Valentin, Alemayehu, Tadesse, Arheimer, Berit, Ayzel, Georgy, Breuer, Lutz, Chamorro, Alejandro, Daggupati, Prasad, Donnelly, Chantal, Eisner, Stephanie, Flörke, Martina, Gao, Chao, Gelfan, Alexander, Gusev, Yeugeniy, Gustafsson, David, Haberlandt, Uwe, Huang, Jinlong, Huang, Shaochun, Hundecha, Yeshewatesfa, Jiang, Tong, Kalugin, Andrei, Koch, Hagen, Kovalev, Evgeny E., Kraft, Philipp, Krylenko, Inna, Kumar, Rohini, Kundu, Dipangkar, Liersch, Stefan, Liu, Suxia, Lobanova, Anastasia, Lavrenov, Alexander, Mishra, Vimal, Mo, Xingguo, Motovilov, Yury, Nasonova, Olga, Van-Ogtrop, Floris, Pechlivanidis, Ilias, Piniewski, Mikolaj, Plötner, Stefan, Reinhardt, Julia, Samaniego, Luis, Seidou, Ousmane, Shah, Harsh, Shi, Pengfei, Strauch, Michael, Su, Buda, Tecklenburg, Julia, Teklesadik, Aklilu, Van Griensven, Ann, Vervoort, Willem, Vetter, Tobias, Wallner, Markus, Wang, Xiaoyan, Wortmann, Michel, Yang, Tao, Zeng, Xiaofan, Büchner, Matthias, Schewe, Jacob, Zhao, Fang
Published 2017

Thirteen thousand years of southeastern Mediterranean climate variability inferred from an integrative planktic foraminiferal-based approach

by Mojtahid, Meryem, Manceau, R., Schiebel, Ralf, Hennekam, R., de Lange, G.-J.
Published in Paleoceanography (2015)