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zenodo40/100

Fig. 1 in Winter Diet Of The Common Genet, Genetta Genetta (Carnivora, Viverridae), And The African Golden Wolf, Canis Anthus (Carnivora, Canidae), In Altitudinal Locality Of The Edough Forest (Northeastern Algeria)

Fig. 1. Geographical situation of the study locality. (with indication of the three transects: 1, 2 and 3). Source: https://journals.openedition.org/physio-geo/docannexe/image/4217/img-1.jpg. Modified by Boukheroufa (present work).

opencc-by-4.0Mar 2020View details →
zenodo36/100

Fig. 3 in Winter Diet Of The Common Genet, Genetta Genetta (Carnivora, Viverridae), And The African Golden Wolf, Canis Anthus (Carnivora, Canidae), In Altitudinal Locality Of The Edough Forest (Northeastern Algeria)

Fig. 3. Occurrence frequency of different food categories for both species.

opencc-by-4.0Mar 2020View details →
zenodo36/100

Fig. 4 in Winter Diet Of The Common Genet, Genetta Genetta (Carnivora, Viverridae), And The African Golden Wolf, Canis Anthus (Carnivora, Canidae), In Altitudinal Locality Of The Edough Forest (Northeastern Algeria)

Fig. 4. Diets of the African golden wolf (left) and the common genet (right) in the study area.

opencc-by-4.0Mar 2020View details →
zenodo36/100

Fig. 2 in Winter Diet Of The Common Genet, Genetta Genetta (Carnivora, Viverridae), And The African Golden Wolf, Canis Anthus (Carnivora, Canidae), In Altitudinal Locality Of The Edough Forest (Northeastern Algeria)

Fig. 2. All food categories consumed by the two predators (©: M. Boukheroufa).

opencc-by-4.0Mar 2020View details →
zenodo32/100

FIGURE 2 in Nomenclatural comments on the Rusty-spotted Genet (Carnivora, Viverridae) and designation of a neotype

FIGURE 2. Genetta maculata, neotype (left; MNHN 1972-395), Genetta maculata (middle: MNHN 1907-586; Ethiopia) and Genetta pardina (right; MNHN 1977-711; Senegal). Skulls in dorsal view (a), ventral view (b) and lateral view (c). Black arrows indicate the diagnostic characters for G. maculata as quoted in the text.

opennotspecifiedMar 2003View details →
zenodo32/100

FIGURE 1 in Nomenclatural comments on the Rusty-spotted Genet (Carnivora, Viverridae) and designation of a neotype

FIGURE 1. Genetta maculata, neotype (a; MNHN 1972-395), Genetta maculata, iconotype (b; from Gray, 1830), Genetta maculata (c; MNHN 1965-338; Cameroon) and Genetta pardina (d; MNHN 1977-711; Senegal). Black arrows indicate the diagnostic characters for G. maculata as quoted in the text.

opennotspecifiedMar 2003View details →
zenodo32/100

Figure 4 in The distribution of the Malay civet Viverra tangalunga (Carnivora: Viverridae) across Southeast Asia: natural or human-mediated dispersal?

Figure 4. Mismatch distribution computed for the concatenated mitochondrial sequences for all samples, and for the different populations (Peninsular Malaysia, Borneo, Philippines, Sulawesi, and Moluccas); solid line, observed distribution of pairwise differences; dashed line, expected distribution under the model of sudden demographic expansion.

opennotspecifiedFeb 2014View details →
zenodo32/100

Figure 2. Phylogenetic relationships among Viverra tangalunga inferred from mtDNA haplotypes from the concatenated 797 in The distribution of the Malay civet Viverra tangalunga (Carnivora: Viverridae) across Southeast Asia: natural or human-mediated dispersal?

Figure 2. Phylogenetic relationships among Viverra tangalunga inferred from mtDNA haplotypes from the concatenated 797-bp mitochondrial control region and cytochrome b sequences. Trees for each of the three analyses (neighbour joining, maximum likelihood, and Bayesian inference) had similar topologies. Numbers above the branches represent bootstrap support, with only values> 60% shown. Numbers in parentheses represent the number of individuals sharing the same haplotype; haplotype codes are listed in Appendix S3.

opennotspecifiedFeb 2014View details →
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Figure 1 in The distribution of the Malay civet Viverra tangalunga (Carnivora: Viverridae) across Southeast Asia: natural or human-mediated dispersal?

Figure 1. The location of Viverra tangalunga samples used in this study. The grey shading indicates the currently known distribution of V. tangalunga (see Jennings & Veron, 2011). The size of each dot represents the number of samples per locality.

opennotspecifiedFeb 2014View details →
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Subspecies and Distribution. H. d. derbyanus Gray, 1837 — Myanmar, Thailand, Peninsular Malaysia, Sumatra, Siberut I, and Borneo. H. d. minor G.S. Miller, 1913 — South Pagai I. H. d. sipora Chasen & Kloss, 1928 — Sipora I. in Viverridae

Subspecies and Distribution. H. d. derbyanus Gray, 1837 — Myanmar, Thailand, Peninsular Malaysia, Sumatra, Siberut I, and Borneo. H. d. minor G.S. Miller, 1913 — South Pagai I. H. d. sipora Chasen & Kloss, 1928 — Sipora I.

opennotspecifiedJan 2009View details →
zenodo32/100

Distribution. Myanmar, Thailand, Peninsular Malaysia, Singapore, Sumatra, and Borneo. There is one skin from N Vietnam (Tonkin, the type locality of C. lowei) and a possible skin record in China (S Yunnan). However, there have been no further confirmed records from these two areas. in Viverridae

Distribution. Myanmar, Thailand, Peninsular Malaysia, Singapore, Sumatra, and Borneo. There is one skin from N Vietnam (Tonkin, the type locality of C. lowei) and a possible skin record in China (S Yunnan). However, there have been no further confirmed records from these two areas.

opennotspecifiedJan 2009View details →
zenodo32/100

Subspecies and Distribution. P.j. jerdoni Blanford, 1885 — SW India (Western Ghats). P. j. caniscus Pocock, 1933 — S India (Palni Hills, Tamil Nadu). in Viverridae

Subspecies and Distribution. P.j. jerdoni Blanford, 1885 — SW India (Western Ghats). P. j. caniscus Pocock, 1933 — S India (Palni Hills, Tamil Nadu).

opennotspecifiedJan 2009View details →
zenodo32/100

Distribution. Pakistan, India, Sri Lanka, and Nepal to China, Mainland SE Asia, Peninsular Malaysia, Sumatra, Java, Borneo, the Philippines, and many ssa small islands. Also scattered records in Sulawesi, Moluccan Is, Timor, and the Aru Is, probably resulting from introductions. Presence uncertain in Papua New Guinea. Introduced to Japan in the late 1800s. in Viverridae

Distribution. Pakistan, India, Sri Lanka, and Nepal to China, Mainland SE Asia, Peninsular Malaysia, Sumatra, Java, Borneo, the Philippines, and many ssa small islands. Also scattered records in Sulawesi, Moluccan Is, Timor, and the Aru Is, probably resulting from introductions. Presence uncertain in Papua New Guinea. Introduced to Japan in the late 1800s.

opennotspecifiedJan 2009View details →
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Subspecies and Distribution. P. l. larvata C. E. H. Smith, 1827 — China (and Taiwan & Hainan Is), Cambodia, Laos, Myanmar, and Vietnam. P. l. annectens Robinson & Kloss, 1917 — Peninsular Malaysia and Thailand. P. l. grayi Bennett, 1835 — Bhutan, India, Nepal, and Pakistan. P. l. leucocephala Gray 1865 — Borneo. P. l. leucomystax Gray, 1837 — Sumatra. P. l. tytlerii Tytler, 1864 — Andaman Is. A possible sighting in western Java in 1993; however, there are no other records for this island. Introduced to Japan. in Viverridae

Subspecies and Distribution. P. l. larvata C. E. H. Smith, 1827 — China (and Taiwan & Hainan Is), Cambodia, Laos, Myanmar, and Vietnam. P. l. annectens Robinson & Kloss, 1917 — Peninsular Malaysia and Thailand. P. l. grayi Bennett, 1835 — Bhutan, India, Nepal, and Pakistan. P. l. leucocephala Gray 1865 — Borneo. P. l. leucomystax Gray, 1837 — Sumatra. P. l. tytlerii Tytler, 1864 — Andaman Is. A possible sighting in western Java in 1993; however, there are no other records for this island. Introduced to Japan.

opennotspecifiedJan 2009View details →
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Distribution. E in Viverridae

Distribution. E Nepal, NE India (Sikkim, Assam & Arunachal Pradesh), Bhutan, Bangladesh, S China (Yunnan, Guangxi), Mainland SE Asia, Peninsular Malaysia, Indonesia (Sumatra, Java, Nias, Bangka, Bintan & Kundur Is), and the Philippines (Calauit & Palawan Is).

opennotspecifiedJan 2009View details →
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Subspecies and Distribution. V. z. zibetha Linnaeus, 1758 — SW China (Xizang) to Nepal and NE India. V. z. expectata Colbert & Hooijer, 1953 — China. V.z. sigillata Robinson & Kloss, 1920 — Thailand and Peninsular Malaysia. V. z. hainana Wang & Xu, 1983 — China (Hainan I). V. z. pruinosus Wroughton, 1915 — Myanmar. V. z. surdaster Thomas, 1927 — Cambodia, Laos and Vietnam. Introduced to the Andaman Islands. in Viverridae

Subspecies and Distribution. V. z. zibetha Linnaeus, 1758 — SW China (Xizang) to Nepal and NE India. V. z. expectata Colbert & Hooijer, 1953 — China. V.z. sigillata Robinson & Kloss, 1920 — Thailand and Peninsular Malaysia. V. z. hainana Wang & Xu, 1983 — China (Hainan I). V. z. pruinosus Wroughton, 1915 — Myanmar. V. z. surdaster Thomas, 1927 — Cambodia, Laos and Vietnam. Introduced to the Andaman Islands.

opennotspecifiedJan 2009View details →
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Subspecies and Distribution. V. t. tangalunga Gray, 1832 — Peninsular Malaysia, Sumatra, Borneo, several Indonesian islands (Amboina I, Banggi I, Langkawi I, Rhio-Lingga Archipelago, Bangka I, Karimata I & Sulawesi), and the Philippines; also two records from Java, but no evidence of native population. V. t. lankavensis Robinson & Kloss, 1920 — Malaysia (Langkawi I). in Viverridae

Subspecies and Distribution. V. t. tangalunga Gray, 1832 — Peninsular Malaysia, Sumatra, Borneo, several Indonesian islands (Amboina I, Banggi I, Langkawi I, Rhio-Lingga Archipelago, Bangka I, Karimata I & Sulawesi), and the Philippines; also two records from Java, but no evidence of native population. V. t. lankavensis Robinson & Kloss, 1920 — Malaysia (Langkawi I).

opennotspecifiedJan 2009View details →
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Subspecies and Distribution. C. c. civetta Schreber, 1776 — S Mauritania and Senegal E to Ethiopia and Somalia, and S to Gabon. C. c. australis Lundholm, 1955 — Zambia and E Botswana to Malawi and Mozambique, and S to South Africa and Swaziland. C. c. congica Cabrera, 1929 — S Sudan, DR Congo and Rwanda, S to Angola and N Zambia. C. c. pauli Kock, Kunzel & Rayaleh, 2000 — Djibouti. C. c. schwarz Cabrera, 1929 — S Somalia, Kenya, Uganda, and Tanzania (including Zanzibar I). C. c. volkmanni: Lundholm, 1955 — NE Namibia and N Botswana. in Viverridae

Subspecies and Distribution. C. c. civetta Schreber, 1776 — S Mauritania and Senegal E to Ethiopia and Somalia, and S to Gabon. C. c. australis Lundholm, 1955 — Zambia and E Botswana to Malawi and Mozambique, and S to South Africa and Swaziland. C. c. congica Cabrera, 1929 — S Sudan, DR Congo and Rwanda, S to Angola and N Zambia. C. c. pauli Kock, Kunzel & Rayaleh, 2000 — Djibouti. C. c. schwarz Cabrera, 1929 — S Somalia, Kenya, Uganda, and Tanzania (including Zanzibar I). C. c. volkmanni: Lundholm, 1955 — NE Namibia and N Botswana.

opennotspecifiedJan 2009View details →
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Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40. in Viverridae

Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40.

opennotspecifiedJan 2009View details →
zenodo32/100

Subspecies and Distribution. V. i. indica Geoffroy Saint-Hilaire, 1803 — S peninsular India. V. i. atchinensis Sody, 1931 — Sumatra. V. i. baliensis Sody, 1931 — Bali. V. i. baptistae Pocock, 1933 — Bangladesh to NE India (Assam), and Bhutan. V. i. deserti Bonhote, 1898 — Pakistan through C India to Nepal. V. i. klossi Pocock, 1933 — Malaysia. V. i. mayori Pocock, 1933 — Sri Lanka. V. i. muriavensis Sody, 1931 — Java. V.i. taivana Schwarz, 1911 — Taiwan. V.i. thai Kloss, 1919 — Myanmar and Thailand through Indochina to China. V. i. wellsi Pocock, 1933 — NW India. It has been introduced to Madagascar, Zanzibar Island, the Comoro Islands, and Socotra Island for the production of civet or to be used as rat catchers; its presence on some of the Indonesian islands (Bali, Bawean, Kangean, Lombok, and Sumbawa) could also have resulted from introductions. in Viverridae

Subspecies and Distribution. V. i. indica Geoffroy Saint-Hilaire, 1803 — S peninsular India. V. i. atchinensis Sody, 1931 — Sumatra. V. i. baliensis Sody, 1931 — Bali. V. i. baptistae Pocock, 1933 — Bangladesh to NE India (Assam), and Bhutan. V. i. deserti Bonhote, 1898 — Pakistan through C India to Nepal. V. i. klossi Pocock, 1933 — Malaysia. V. i. mayori Pocock, 1933 — Sri Lanka. V. i. muriavensis Sody, 1931 — Java. V.i. taivana Schwarz, 1911 — Taiwan. V.i. thai Kloss, 1919 — Myanmar and Thailand through Indochina to China. V. i. wellsi Pocock, 1933 — NW India. It has been introduced to Madagascar, Zanzibar Island, the Comoro Islands, and Socotra Island for the production of civet or to be used as rat catchers; its presence on some of the Indonesian islands (Bali, Bawean, Kangean, Lombok, and Sumbawa) could also have resulted from introductions.

opennotspecifiedJan 2009View details →

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