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Subspecies and Distribution. P.m.mediusTemminck,1825—WPakistan,India(exceptNE),SriLanka,Bangladesh,WMyanmar,andAndamanIs. P.m.arielG.M.Allen,1908—MaldivesIs. P. m. leucocephalus Hodgson, 1835 — Nepal, NE India (Sikkim, Assam, and Manipur), and Bhutan. in Pteropodidae
Subspecies and Distribution. P.m.mediusTemminck,1825—WPakistan,India(exceptNE),SriLanka,Bangladesh,WMyanmar,andAndamanIs. P.m.arielG.M.Allen,1908—MaldivesIs. P. m. leucocephalus Hodgson, 1835 — Nepal, NE India (Sikkim, Assam, and Manipur), and Bhutan.
FIGURE. Dicorynia paraensis, var. ingens, var. macrophylla and floral diagram to D. paraensis. A–C. Dicorynia paraensis var. macrophylla; A. Branch with leaves; B. Axillary bud; C. Petiolule and base of the leaflet; D–G. Dicorynia paraensis var. ingens; D. Branch with a leaf; E. Axillary bud; F. Petiolule and base of the leaflet; G. Detail of the abaxial face of the leaflet presenting dark glandular trichomes; H. Floral diagram of D. paraensis, arrows represent bracts and asterisks represent lateral flowers in a cymose subunit. A: D. Cardoso 3397; B–C: A. Ducke s.n. RB231037; D–G: A. Ducke s.n. MG16022. Drawn by M. Falcão. Scale bar. A, D: 3 cm; B–C, E–F: 2mm; G: 0.1mm. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)
FIGURE. Dicorynia paraensis, var. ingens, var. macrophylla and floral diagram to D. paraensis. A–C. Dicorynia paraensis var. macrophylla; A. Branch with leaves; B. Axillary bud; C. Petiolule and base of the leaflet; D–G. Dicorynia paraensis var. ingens; D. Branch with a leaf; E. Axillary bud; F. Petiolule and base of the leaflet; G. Detail of the abaxial face of the leaflet presenting dark glandular trichomes; H. Floral diagram of D. paraensis, arrows represent bracts and asterisks represent lateral flowers in a cymose subunit. A: D. Cardoso 3397; B–C: A. Ducke s.n. RB231037; D–G: A. Ducke s.n. MG16022. Drawn by M. Falcão. Scale bar. A, D: 3 cm; B–C, E–F: 2mm; G: 0.1mm.
FIGURE. Seedlings, seeds, embryos, anthers, and pollen in Dicorynia. A–D. Different stages of development in seedlings of D. paraensis, First eophiles unifoliolate and opposite; E–G. Seed of D. guianensis: E. External surface; F. Endosperm of the longitudinally sectioned seed, note the slightly gelatinous upper region; G. Cotyledon and embryo of longitudinally sectioned seed; H. SEM of seed's testa in D. paraensis; I. SEM of endosperm's surface in D. guianensis (notice the presence of circular perforations); J–K. SEM of the hypocotyl-radicular axis of the seed in D. guianensis and D. paraensis; L. SEM of seed's testa in D. guianensis; M–N. SEM of plumule region in embryo of D. guianensis and D. paraensis (note the developed leaf primordia); O. Apex of anther in longer stamen of D. paraensis, showing 4 sporangia and two pores covered by an apicle; P. Apex of anther in shorter stamen of D. guianensis, at least 9 sporangia; Q. Apex of anther in longer stamen of D. guianensis, 8 sporangia; R. Pollen grains in D. paraensis. A–D: Falcão, M.J. 91; E–G, I–J, L–M: Gentry 63030; H, K, N: Berry, P.E. 7460; O: Amaral, E. 618; P, Q: Unknown collector MO1576407; Scale bar. A–D: 2cm; E–G: 3mm; H–L: 1mm; M–N: 100 μm; O-Q: 200μm; R: 5 μm. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)
FIGURE. Seedlings, seeds, embryos, anthers, and pollen in Dicorynia. A–D. Different stages of development in seedlings of D. paraensis, First eophiles unifoliolate and opposite; E–G. Seed of D. guianensis: E. External surface; F. Endosperm of the longitudinally sectioned seed, note the slightly gelatinous upper region; G. Cotyledon and embryo of longitudinally sectioned seed; H. SEM of seed's testa in D. paraensis; I. SEM of endosperm's surface in D. guianensis (notice the presence of circular perforations); J–K. SEM of the hypocotyl-radicular axis of the seed in D. guianensis and D. paraensis; L. SEM of seed's testa in D. guianensis; M–N. SEM of plumule region in embryo of D. guianensis and D. paraensis (note the developed leaf primordia); O. Apex of anther in longer stamen of D. paraensis, showing 4 sporangia and two pores covered by an apicle; P. Apex of anther in shorter stamen of D. guianensis, at least 9 sporangia; Q. Apex of anther in longer stamen of D. guianensis, 8 sporangia; R. Pollen grains in D. paraensis. A–D: Falcão, M.J. 91; E–G, I–J, L–M: Gentry 63030; H, K, N: Berry, P.E. 7460; O: Amaral, E. 618; P, Q: Unknown collector MO1576407; Scale bar. A–D: 2cm; E–G: 3mm; H–L: 1mm; M–N: 100 μm; O-Q: 200μm; R: 5 μm.
FIGURE. Distribution of Dicorynia. Physical map of the Amazonian region with all analyzed specimens of Dicorynia. A large amount of point overlays leading to reduced number of visible points is due to the large percentage of materials being old collections that rely only on the name of the municipality or similar. Source: NASA with modifications. Note that almost all specimens are contained in areas with less than 200 m high and the high elevations of the Guiana shield may represent a form of isolation between the two species. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)
FIGURE. Distribution of Dicorynia. Physical map of the Amazonian region with all analyzed specimens of Dicorynia. A large amount of point overlays leading to reduced number of visible points is due to the large percentage of materials being old collections that rely only on the name of the municipality or similar. Source: NASA with modifications. Note that almost all specimens are contained in areas with less than 200 m high and the high elevations of the Guiana shield may represent a form of isolation between the two species.
Supplementary material 2 from: Sturm U, Heyne E, Herrmann E, Arends B, Dieter A-L, Dorfman E, Drauschke F, Heller N, Kahn R, Kaiser K, Koch G, Kramar N, Mansilla Sánchez A, Mauelshagen F, Nadim T, Pell R, Petersen M, Schmidt-Loske K, Scholz H, Sterling C, Trischler H, Wagner S (2022) Anthropocenic Objects. Collecting Practices for the Age of Humans. Research Ideas and Outcomes 8: e89446. https://doi.org/10.3897/rio.8.e89446
Flyer: How to collect, store and curate objects in the Anthropocene? On participatory and digital collections.
Supplementary material 1 from: Sturm U, Heyne E, Herrmann E, Arends B, Dieter A-L, Dorfman E, Drauschke F, Heller N, Kahn R, Kaiser K, Koch G, Kramar N, Mansilla Sánchez A, Mauelshagen F, Nadim T, Pell R, Petersen M, Schmidt-Loske K, Scholz H, Sterling C, Trischler H, Wagner S (2022) Anthropocenic Objects. Collecting Practices for the Age of Humans. Research Ideas and Outcomes 8: e89446. https://doi.org/10.3897/rio.8.e89446
Flyer: What is an Anthropocenic Object? Transdisciplinary Perspectives on Natural, Cultural and Hybrid Objects
Supplementary material 4 from: Sturm U, Heyne E, Herrmann E, Arends B, Dieter A-L, Dorfman E, Drauschke F, Heller N, Kahn R, Kaiser K, Koch G, Kramar N, Mansilla Sánchez A, Mauelshagen F, Nadim T, Pell R, Petersen M, Schmidt-Loske K, Scholz H, Sterling C, Trischler H, Wagner S (2022) Anthropocenic Objects. Collecting Practices for the Age of Humans. Research Ideas and Outcomes 8: e89446. https://doi.org/10.3897/rio.8.e89446
Keynote Exhibiting the Anthropocene - and the Technosphere - means breaking away from established knowledge orders
Subspecies and Distribution. S.t.townsendiiBachman,1839—fromextremeSWBritishColumbia(SWCanada)SthroughWWashingtonandWOregontoNWCalifornia(NWUSA). S. t. olympicus M. L. Johnson & Yates, 1980 — known only from elevations above 1000 m in Olympic National Park, NW Washington (USA). in Talpidae
Subspecies and Distribution. S.t.townsendiiBachman,1839—fromextremeSWBritishColumbia(SWCanada)SthroughWWashingtonandWOregontoNWCalifornia(NWUSA). S. t. olympicus M. L. Johnson & Yates, 1980 — known only from elevations above 1000 m in Olympic National Park, NW Washington (USA).
FIGURES 19–33. Macropsidius spp., calling signal oscillograms. 19–23―M in Macropsidius bogutensis (Mityaev, 1990) species group (Hemiptera: Auchenorrhyncha: Cicadellidae: Eurymelinae: Macropsini) in Kazakhstan: taxonomy, biology, and evolution
FIGURES 19–33. Macropsidius spp., calling signal oscillograms. 19–23―M. karatavicus sp. n., 24–28―M. bogutensis, 29– 33―M. kajkanus. Faster oscillograms of the parts of signals indicated as "21–22", "26–28", and "32–33" are given under the same numbers.
Subspecies and Distribution. M.b.bobakP.L..S.Muller,1776—EUkraineandacrossSRussiatotheVolgaRiver. M.b.kozloviFokanov,1966—CpartofthedistributionEoftheVolgaRiver,nearUlyanovsk(Russia)withuncertainEboundary. M. b. tschaganensis Bazhanov, 1930 — E part of the distribution in Kazakhstan with uncertain W boundary. Introduced into the Caucasus Mts (Dagestan, Russia). in Sciuridae
Subspecies and Distribution. M.b.bobakP.L..S.Muller,1776—EUkraineandacrossSRussiatotheVolgaRiver. M.b.kozloviFokanov,1966—CpartofthedistributionEoftheVolgaRiver,nearUlyanovsk(Russia)withuncertainEboundary. M. b. tschaganensis Bazhanov, 1930 — E part of the distribution in Kazakhstan with uncertain W boundary. Introduced into the Caucasus Mts (Dagestan, Russia).
Subspecies and Distribution. M.m.mimulusThomas,1898—SWColombiaandNWEcuador. M.m.boguetensisNelson,1903—nearlyallofPanama,andextendingintoNWColombia. M. m. isthmus Nelson, 1899 — SW Panama and W Colombia. in Sciuridae
Subspecies and Distribution. M.m.mimulusThomas,1898—SWColombiaandNWEcuador. M.m.boguetensisNelson,1903—nearlyallofPanama,andextendingintoNWColombia. M. m. isthmus Nelson, 1899 — SW Panama and W Colombia.
Subspecies and Distribution. M. m. marmota Linnaeus, 1758 — Alps in Germany, Austria, Switzerland, France, and Italy. M. m. latirostris Kratochvil, 1961 — High Tatra Mts of Slovakia and Poland. Nominate subspecies reintroduced to Romania (Carpathian Mts) and Slovenia (Julian Alps), and introduced into the Black Forest (Germany), the Massif Central, Jura, and Vosgues (France), the Pyrenees (France, Spain, and Andorra), E Austria, Apennine Mts (Italy), N Serbia, Montenegro. in Sciuridae
Subspecies and Distribution. M. m. marmota Linnaeus, 1758 — Alps in Germany, Austria, Switzerland, France, and Italy. M. m. latirostris Kratochvil, 1961 — High Tatra Mts of Slovakia and Poland. Nominate subspecies reintroduced to Romania (Carpathian Mts) and Slovenia (Julian Alps), and introduced into the Black Forest (Germany), the Massif Central, Jura, and Vosgues (France), the Pyrenees (France, Spain, and Andorra), E Austria, Apennine Mts (Italy), N Serbia, Montenegro.
Distribution. Restricted to three montane swamps (2100-2300 m) in E DR Congo (Mt Kahuzi) and high-elevation swamps in SW Uganda (Echuya Forest, Ngoto Swamp, Ruhija, Mubwindi Swamp, and Bwindi Impenetrable National Park) at 1500-2380 m. Extensive surveys in swamps in Burundi and Rwenzori Mts have notyielded any specimens. in Soricidae
Distribution. Restricted to three montane swamps (2100-2300 m) in E DR Congo (Mt Kahuzi) and high-elevation swamps in SW Uganda (Echuya Forest, Ngoto Swamp, Ruhija, Mubwindi Swamp, and Bwindi Impenetrable National Park) at 1500-2380 m. Extensive surveys in swamps in Burundi and Rwenzori Mts have notyielded any specimens.
Subspecies and Distribution. M.l.longicaudatusMeester&Dippenaar,1978—KnysnaForest,SWSouthAfrica. M. l. boosnami Dippenaar, 1995 — Boosmansbos Forest and Langeberg Mts, SW South Africa. in Soricidae
Subspecies and Distribution. M.l.longicaudatusMeester&Dippenaar,1978—KnysnaForest,SWSouthAfrica. M. l. boosnami Dippenaar, 1995 — Boosmansbos Forest and Langeberg Mts, SW South Africa.
Subspecies and Distribution. C.m.mariquensisA.Smith,1844—ESouthAfrica,Swaziland,andSMozambique. C.m.neavetWroughton,1907—WCAngola,SDRCongo,andZambia. C. m. shortridgei St. Leger, 1932 — NE Namibia, N Botswana, and extreme NW Zimbabwe. in Soricidae
Subspecies and Distribution. C.m.mariquensisA.Smith,1844—ESouthAfrica,Swaziland,andSMozambique. C.m.neavetWroughton,1907—WCAngola,SDRCongo,andZambia. C. m. shortridgei St. Leger, 1932 — NE Namibia, N Botswana, and extreme NW Zimbabwe.
Distribution. Restricted to the Kahuzi Mts in E DR Congo; confined to a small montane region W of Lake Kivu between Lwiro and Mt Kahuzi (1700-3300 m). Probably widely distributed in undisturbed areas above 2000 m. in Soricidae
Distribution. Restricted to the Kahuzi Mts in E DR Congo; confined to a small montane region W of Lake Kivu between Lwiro and Mt Kahuzi (1700-3300 m). Probably widely distributed in undisturbed areas above 2000 m.
Distribution. Endemic to relict forest patches at elevations over 1500 m in the Rungwe and Udzungwa Mts in S Tanzania. Not known from any of the other Eastern Arc Mts in Tanzania. in Soricidae
Distribution. Endemic to relict forest patches at elevations over 1500 m in the Rungwe and Udzungwa Mts in S Tanzania. Not known from any of the other Eastern Arc Mts in Tanzania.
Distribution. Endemic to Eastern Arc Mts in Tanzania (Uluguru and Udzungwa Mts), at elevations of ¢.600-1150 m. in Soricidae
Distribution. Endemic to Eastern Arc Mts in Tanzania (Uluguru and Udzungwa Mts), at elevations of ¢.600-1150 m.
Subspecies and Distribution. C. r rapax G. M. Allen, 1923 — S China including the mainland (Sichuan, Yunnan, Guizhou, Hunan, and Guangxi) and Hainan I, adjacent N Myanmar, NE India (Meghalaya, but exact locality not known), and S Vietnam. It might have a larger range than currently recognized. C.r.kurodaiJameson&G.S.Jones,1977—Taiwan1 C.r.lutaoensisFangYinping&LeeLingling,2002—GreenI(Lutao),offSETaiwanI. C. r. tadae Tokuda & Kano, 1936 — Orchid I (Lanyu), off SE Taiwan I. in Soricidae
Subspecies and Distribution. C. r rapax G. M. Allen, 1923 — S China including the mainland (Sichuan, Yunnan, Guizhou, Hunan, and Guangxi) and Hainan I, adjacent N Myanmar, NE India (Meghalaya, but exact locality not known), and S Vietnam. It might have a larger range than currently recognized. C.r.kurodaiJameson&G.S.Jones,1977—Taiwan1 C.r.lutaoensisFangYinping&LeeLingling,2002—GreenI(Lutao),offSETaiwanI. C. r. tadae Tokuda & Kano, 1936 — Orchid I (Lanyu), off SE Taiwan I.
Distribution. Known only from the type locality in Huong Son district, Ha Tinh Province, NC Vietnam, at elevations of 920-1240 m; it likely occurs at higher elevations throughout the N Annamite Range and may be expected on bordering Laos. in Soricidae
Distribution. Known only from the type locality in Huong Son district, Ha Tinh Province, NC Vietnam, at elevations of 920-1240 m; it likely occurs at higher elevations throughout the N Annamite Range and may be expected on bordering Laos.
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