Search Results

FIGURE 5 in Type specimens of birds in the Natural History Museum, University of Oslo, Norway

by Johannessen, Lars Erik, Lifjeld, Jan T.
Published 2022

FIGURE 4 in Type specimens of birds in the Natural History Museum, University of Oslo, Norway

by Johannessen, Lars Erik, Lifjeld, Jan T.
Published 2022

Effects of ocean acidification on embryonic respiration and development of a temperate wrasse living along a natural CO2 gradient

by Cattano, Carlo, Giomi, Folco, Milazzo, Marco
Published 2016

Effects of ocean acidification on embryonic respiration and development of a temperate wrasse living along a natural CO2 gradient, supplement to: Cattano, Carlo; Giomi, Folco; Milazzo, Marco (2016...

by Cattano, Carlo, Giomi, Folco, Milazzo, Marco
Published 2016

Distribution. Arctic areas of Alaska, Canada, and NE & N Greenland. Successfully introduced into W & SW Greenland, Norway, Russia, and several areas of Alaska outside their natural range. in Bovidae

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

Plate 1 from: Hoffmann D, Geller-Grimm F (2013) A catalog of bird specimens associated with Prince Maximilian of Wied-Neuwied and potential type material in the natural history collection in Wiesbaden...

by Hoffmann, Dorothee, Geller-Grimm, Fritz
Published 2013

Seawater carbonate chemistry, length and survival of Inland silverside, Menidia beryllina, during experiments, 2012, supplement to: Baumann, Hannes; Talmage, Stephanie C; Gobler, Christopher J (2012): Reduced early life growth and survival in a fish in direct response to increased carbon dioxide. Nature Climate...

by Baumann, Hannes, Talmage, Stephanie C, Gobler, Christopher J
Published 2011

Effects of elevated CO2 on fish behaviour undiminished by transgenerational acclimation, supplement to: Welch, Megan J; Watson, Sue-Ann; Welsh, Justin Q; McCormick, Mark I; Munday, Philip L (2014): Effects of elevated CO2 on fish behaviour undiminished by transgenerational acclimation. Nature Climate Change, 4(12...

by Welch, Megan J, Watson, Sue-Ann, Welsh, Justin Q, McCormick, Mark I, Munday, Philip L
Published 2014

Seawater carbonate chemistry and gene expression of a reef fish Acanthochromis polyacanthus, supplement to: Schunter, Celia; Welch, Megan J; Nilsson, Göran E; Rummer, Jodie L; Munday, Philip L; Ravasi, Timothy (2018): An interplay between plasticity and parental phenotype determines impacts of ocean acidification on a reef fish. Nature Ecology & Evolution, 2(2), 334-342

by Schunter, Celia, Welch, Megan J, Nilsson, Göran E, Rummer, Jodie L, Munday, Philip L, Ravasi, Timothy
Published 2018

Seawater carbonate chemistry and gene expression of a reef fish Acanthochromis polyacanthus, supplement to: Schunter, Celia; Welch, Megan J; Nilsson, Göran E; Rummer, Jodie L; Munday, Philip L; Ravasi, Timothy (2018): An interplay between plasticity and parental phenotype determines impacts of ocean acidification on a reef fish. Nature Ecology & Evolution, 2(2), 334-342

by Schunter, Celia Marei, Welch, Megan J., Nilsson, Göran E., Rummer, Jodie L., Munday, Philip L., Ravasi, Timothy
Published 2019

Seawater carbonate chemistry and fish Amphiprion percula behaviour during experiments, 2012, supplement to: Nilsson, Göran E; Dixson, Danielle L; Domenici, Paolo; McCormick, Mark I; Sorensen, Christina; Watson, Sue-Ann; Munday, Philip L (2012): Near-future carbon dioxide levels alter fish behaviour by interfering with neurotransmitter function. Nature Climate Change, 2, 201-204

by Nilsson, Göran E, Dixson, Danielle L, Domenici, Paolo, McCormick, Mark I, Sorensen, Christina, Watson, Sue-Ann, Munday, Philip L
Published 2012

Seawater carbonate chemistry and length, weight, survival rate, metabolic rate of coral reef fish Amphiprion melanopus in a laboratory experiment, supplement to: Miller, Garielle M; Watson, Sue-Ann; Donelson, Jennifer M; McCormick, Mark I; Munday, Philip L (2012): Parental environment mediates impacts of increased carbon dioxide on a coral reef fish. Nature Climate Change, 2(12), 858-861

by Miller, Garielle M, Watson, Sue-Ann, Donelson, Jennifer M, McCormick, Mark I, Munday, Philip L
Published 2012

Seawater carbonate chemistry and Oikopleura dioica survival, growth, developmental and maturation kinetics in microcosm experiment

by Bouquet, Jean-Marie, Troedsson, Christofer, Novac, Aliona, Reeve, Magnus, Lechtenbörger, Anna K, Massart, Wendy, Skaar, Katrine S, Aasjord, Anne, Dupont, Sam, Thompson, Eric M
Published 2018

Seawater carbonate chemistry and Oikopleura dioica survival, growth, developmental and maturation kinetics in microcosm experiment

by Bouquet, Jean-Marie, Troedsson, Christofer, Novac, Aliona, Reeve, Magnus, Lechtenbörger, Anna K, Massart, Wendy, Skaar, Katrine S, Aasjord, Anne, Dupont, Sam, Thompson, Eric M
Published 2018

Coarse Filter Ecosystem Management in a Nonequilibrating Forest

by Armstrong, Glen W., Adamowicz, Wiktor L., Beck, Jr, James A., Cummings, Steven G., Schmiegelow, Fiona
Published 2003

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 the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently...

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 the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently...

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

Pipistrellus coromandra Gray 1838

by Struebig, Matthew J., Rossiter, Stephen J., Bates, Paul J. J., Kingston, Tigga, Oo, Sai Sein Lin, Nwe, Aye Aye, Aung, Moe Moe, Win, Sein Sein, Mya, Khin Mya
Published 2005

Pipistrellus coromandra Gray 1838

by Struebig, Matthew J., Rossiter, Stephen J., Bates, Paul J. J., Kingston, Tigga, Oo, Sai Sein Lin, Nwe, Aye Aye, Aung, Moe Moe, Win, Sein Sein, Mya, Khin Mya
Published 2005

Canis lupus Linnaeus 1758

by Masseti, Marco
Published 2009