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Distribution. Uncertain, but the type locality is generally accepted to be Mt Kilimanjaro, NE Tanzania; there are further reports of this species throughout W & E Africa (including some recent ones from Uganda), but they cannot be confirmed since most of the specimens have been wrongly attributed. in Soricidae
Distribution. Uncertain, but the type locality is generally accepted to be Mt Kilimanjaro, NE Tanzania; there are further reports of this species throughout W & E Africa (including some recent ones from Uganda), but they cannot be confirmed since most of the specimens have been wrongly attributed.
Distribution. Known with certainty from the type locality in N Pakistan; reported specimens from further localities in Pakistan may belong to Zarudny's White-toothed Shrew (C. zarudny). in Soricidae
Distribution. Known with certainty from the type locality in N Pakistan; reported specimens from further localities in Pakistan may belong to Zarudny's White-toothed Shrew (C. zarudny).
Subspecies and Distribution. C.r.russulaHermann,1780—W&SWEuropeinGermany,Belgium,Netherlands,Luxembourg,N&WSwitzerland,France,Spain,Portugal,andmanycloseoffshoreislands.ApopulationhasbecomeestablishedonGranCanariaIintheCanaryIs,althoughwhenthespecieswaslikelyintroducedisunresolved. C. r. yebalensis Cabrera, 1913 — NW Africa in N Morocco and N Algeria. The Greater White-toothed Shrew has also been recently reported in S Ireland, where it was likely recently introduced, probably representing the subspecies russula. They also seem to have made it to Scilly Is and the Channel Is, where they probably traveled by boat. in Soricidae
Subspecies and Distribution. C.r.russulaHermann,1780—W&SWEuropeinGermany,Belgium,Netherlands,Luxembourg,N&WSwitzerland,France,Spain,Portugal,andmanycloseoffshoreislands.ApopulationhasbecomeestablishedonGranCanariaIintheCanaryIs,althoughwhenthespecieswaslikelyintroducedisunresolved. C. r. yebalensis Cabrera, 1913 — NW Africa in N Morocco and N Algeria. The Greater White-toothed Shrew has also been recently reported in S Ireland, where it was likely recently introduced, probably representing the subspecies russula. They also seem to have made it to Scilly Is and the Channel Is, where they probably traveled by boat.
Distribution. WC Laos, from S Bolikhamsal Province, probably with the Nam Kading River as the N barrier of the distribution, S to C Khammouane Province, at ¢.17° 40' N; there are also reports from the corridor to Nakai-Nam-Theun National Protected Area, and from Khamkeut District, close to Lak Sao (18° 13' N, 104° 47' E). in Cercopithecidae
Distribution. WC Laos, from S Bolikhamsal Province, probably with the Nam Kading River as the N barrier of the distribution, S to C Khammouane Province, at ¢.17° 40' N; there are also reports from the corridor to Nakai-Nam-Theun National Protected Area, and from Khamkeut District, close to Lak Sao (18° 13' N, 104° 47' E).
Distribution. From the Gambia and Upper Senegal rivers through SW Senegal, Gambia, and Guinea-Bissau (absent E of Rio Corubal, except for a supposed sighting at Catio, near the border with Guinea) to NW Guinea (E to Kopulau Camp, 12° 24° N, 13° 34° 48" W); possibly in NW Sierra Leone. Although reported from the Fouta Djallon Highlands in Guinea, there are no published records available to confirm this. in Cercopithecidae
Distribution. From the Gambia and Upper Senegal rivers through SW Senegal, Gambia, and Guinea-Bissau (absent E of Rio Corubal, except for a supposed sighting at Catio, near the border with Guinea) to NW Guinea (E to Kopulau Camp, 12° 24° N, 13° 34° 48" W); possibly in NW Sierra Leone. Although reported from the Fouta Djallon Highlands in Guinea, there are no published records available to confirm this.
Subspecies and Distribution. C.s.satanasWaterhouse,1838—Bioko1(EquatorialGuinea). C. s. anthracinus Le Conte, 1857 — E & SW Cameroon (S of Sanaga River and as far E as the Batouri and Lomié districts), Equatorial Guinea, W & C Gabon (inland to Lopé National Park and with unconfirmed reports of sparse populations E of the Ogooué and Ivindo rivers), and W Republic of the Congo; possibly in NW Angola (Cabinda). in Cercopithecidae
Subspecies and Distribution. C.s.satanasWaterhouse,1838—Bioko1(EquatorialGuinea). C. s. anthracinus Le Conte, 1857 — E & SW Cameroon (S of Sanaga River and as far E as the Batouri and Lomié districts), Equatorial Guinea, W & C Gabon (inland to Lopé National Park and with unconfirmed reports of sparse populations E of the Ogooué and Ivindo rivers), and W Republic of the Congo; possibly in NW Angola (Cabinda).
Distribution. Patchily in forests not more than 350 km inland from the coast in S Nigeria (W limit in forests near Dahomey Gap), W Cameroon, W Equatorial Guinea, W Gabon, and SW of the Republic of Congo (as far S as Conkouati-Douli National Park); there have been unconfirmed reports of its occurrence in Benin, butif it ever did occur there, it may now be extirpated, as was a former population near the Benue River in Nigeria. in Cercopithecidae
Distribution. Patchily in forests not more than 350 km inland from the coast in S Nigeria (W limit in forests near Dahomey Gap), W Cameroon, W Equatorial Guinea, W Gabon, and SW of the Republic of Congo (as far S as Conkouati-Douli National Park); there have been unconfirmed reports of its occurrence in Benin, butif it ever did occur there, it may now be extirpated, as was a former population near the Benue River in Nigeria.
Distribution. NE India (W Arunachal Pradesh State), in the districts of Tawang and West Kameng at elevations of 2000-3000 m; it possibly extends into Bhutan and Xizang Autonomous Region (= Tibet) in S China. There are reports of its occurrence in Mouling National Park in the Upper Siang District of C Arunachal Pradesh, but they have yet to be confirmed. in Cercopithecidae
Distribution. NE India (W Arunachal Pradesh State), in the districts of Tawang and West Kameng at elevations of 2000-3000 m; it possibly extends into Bhutan and Xizang Autonomous Region (= Tibet) in S China. There are reports of its occurrence in Mouling National Park in the Upper Siang District of C Arunachal Pradesh, but they have yet to be confirmed.
Distribution. EC China (25-33° N, 102° 30°-119° 30" E) in E Xizang Autonomous Region (= Tibet), Sichuan, S Gansu, S Shaanxi, Hubei, Anhui, Zhejiang, N Yunnan, Guizhou, Jiangxi, Fujian, N Guangxi, and N Guangdong provinces; W limit in the Yangtze Gorge in W & NW Sichuan and S limit at 23° 48' N, ¢.110° E in Guangxi. The species may range into NE India (Arunachal Pradesh, Assam, and Meghalaya states), although these reports appear to be based on misidentifications. in Cercopithecidae
Distribution. EC China (25-33° N, 102° 30°-119° 30" E) in E Xizang Autonomous Region (= Tibet), Sichuan, S Gansu, S Shaanxi, Hubei, Anhui, Zhejiang, N Yunnan, Guizhou, Jiangxi, Fujian, N Guangxi, and N Guangdong provinces; W limit in the Yangtze Gorge in W & NW Sichuan and S limit at 23° 48' N, ¢.110° E in Guangxi. The species may range into NE India (Arunachal Pradesh, Assam, and Meghalaya states), although these reports appear to be based on misidentifications.
FIGURES 31–36 in First report of the genera Paralobella and Blasconura (Collembola: Neanuridae Neanurinae) from Japan with the description of three new species
FIGURES 31–36. Blasconura cordis sp. nov. 31, labrum; 32, labium; 33, Dorsal tubercles and chaetotaxy of central area on head; 34, ventral side of abdomen; 35, chaetotaxy of tibiotarsus III and unguis; 36, ventral chaetotaxy on head.
FIGURES 25–30 in First report of the genera Paralobella and Blasconura (Collembola: Neanuridae Neanurinae) from Japan with the description of three new species
FIGURES 25–30. Blasconura cordis sp. nov. 25, dorsal tubercles and chaetotaxy (left side of tubercle De on Th. I abnormal); 26, dorsal chaetotaxy of Ant. I–IV; 27, ventral chaetotaxy of Ant. I–IV; 28, chaeta Di1 of abd. V; 29, mandible; 30, maxilla.
FIGURES 19–24 in First report of the genera Paralobella and Blasconura (Collembola: Neanuridae Neanurinae) from Japan with the description of three new species
FIGURES 19–24. Blasconura triangulum sp. nov. 19, labrum; 20, labium; 21, Dorsal tubercles and chaetotaxy of central area on head; 22, ventral side of abdomen; 23, chaetotaxy of tibiotarsus III and unguis; 24, ventral chaetotaxy on head.
FIGURES 13–18 in First report of the genera Paralobella and Blasconura (Collembola: Neanuridae Neanurinae) from Japan with the description of three new species
FIGURES 13–18. Blasconura triangulum sp. nov. 13, dorsal tubercles and chaetotaxy; 14, dorsal chaetotaxy of Ant. I–IV; 15, ventral chaetotaxy of Ant. I–IV; 16, chaeta Di1 of abd. V; 17, mandible; 18, maxilla.
FIGURES 7–11 in First report of the genera Paralobella and Blasconura (Collembola: Neanuridae Neanurinae) from Japan with the description of three new species
FIGURES 7–11. Paralobella kuchierabu sp. nov. 7, labrum; 8, chaetotaxy of lateral area and ventral side on head; 9, labium; 10, ventral side of abdomen; 11, chaetotaxy of tibiotarsus III and unguis.
FIGURES 1–6 in First report of the genera Paralobella and Blasconura (Collembola: Neanuridae Neanurinae) from Japan with the description of three new species
FIGURES 1–6. Paralobella kuchierabu sp. nov. 1, dorsal tubercles and chaetotaxy (left side of tubercle Dl on Th. III abnormal); 2, dorsal chaetotaxy of Ant. III–IV; 3, ventral chaetotaxy of Ant. III–IV; 4, chaeta Di1 of abd. V; 5, mandible; 6, maxilla.
Subspecies and Distribution. P d. delicatulus Gould, 1842 — monsoonal NW & NC Australia, from Pilbara to far NW Queensland, and including the islands of Tent, Augustus, Bigge, Sir Graham Moore, Bathurst, Melville, Marchinbar, Groote Eylandt, and Sir Edward Pellew Group (West, South West, North, and Vanderlin). P. d. pumilus Troughton, 1936 — NE & CE Australia from Cape York S to NE New South Wales, including Fraser I; also reported from Trans Fly plains in S New Guinea. in Muridae
Subspecies and Distribution. P d. delicatulus Gould, 1842 — monsoonal NW & NC Australia, from Pilbara to far NW Queensland, and including the islands of Tent, Augustus, Bigge, Sir Graham Moore, Bathurst, Melville, Marchinbar, Groote Eylandt, and Sir Edward Pellew Group (West, South West, North, and Vanderlin). P. d. pumilus Troughton, 1936 — NE & CE Australia from Cape York S to NE New South Wales, including Fraser I; also reported from Trans Fly plains in S New Guinea.
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Distribution. Recorded as living animal from the vicinity of Lake Habbema (3225 m) and an area close to Mt Trikora, WC New Guinea. Late Quaternary subfossils reported (as Hydromys habbema) from Kelangurr Cave and from alluvial terrace of West Baliem River, at 280-2950 m,Papua Province. Tentative record of habbema from a fissure deposit at 3450 m on Mt Jaya requires confirmation. in Muridae
Distribution. Recorded as living animal from the vicinity of Lake Habbema (3225 m) and an area close to Mt Trikora, WC New Guinea. Late Quaternary subfossils reported (as Hydromys habbema) from Kelangurr Cave and from alluvial terrace of West Baliem River, at 280-2950 m,Papua Province. Tentative record of habbema from a fissure deposit at 3450 m on Mt Jaya requires confirmation.
Mediating effects of Trait Emotional Intelligence on the association between Adverse Childhood Experiences (ACEs) and Self-reported Health
<p>Data for two studies which investigate the role of trait emotional intelligence in resilience following adverse childhood experiences. </p>
Figure 9. Cymothoa bychowskyi Avdeev, 1979 in Redescription and further report of two buccal attaching fish parasitic cymothoids, Ceratothoa carinata (Bianconi, 1869) and Cymothoa bychowskyi Avdeev, 1979 (Crustacea: Isopoda) with a new record from the southern India Ocean
Figure 9. Cymothoa bychowskyi Avdeev, 1979 from Fistularia villosa Klunzinger, ovigerous female (DABFUK/AR-IS-02). A–E, Pleopods 1–5; F, uropod; G, pleotelson and uropods.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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