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470 results for “Timor”

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zenodo32/100

FIGURE 8 in A new species of Stegonotus (Serpentes: Colubridae) from the remnant coastal forests of southern Timor-Leste

FIGURE 8. Lateral head views of the paratypes of Stegonotus nancuro sp. nov., shown as both photographs and line drawings in left and right aspects, in the left and right image columns, respectively. Shown are USNM 579383 (A, A', B, B'), MCZ R- 192767 (C, C', D, D'), and USNM 580550 (E, E', F, F'). The juvenile paratype has a noticeably different head shape from the eyes forward, with a snout that is shorter relative to eye size than in the other specimens. Images not to scale.

opennotspecifiedSep 2021View details →
zenodo32/100

FIGURE 2 in A new species of Stegonotus (Serpentes: Colubridae) from the remnant coastal forests of southern Timor-Leste

FIGURE 2. Schematic dorsal head views of USNM 580549, the holotype of Stegonotus nancuro sp. nov., shown to illustrate the pattern of head scales and other important characters. Scale labels in (A) include internasals (IN), internasal suture (InS – distance between Points 1 and 2), prefrontals (PF), prefrontal suture (PfS – distance between Points 3 and 4), frontal (F), frontal length (FL – distance between Points 4 and 5), frontal width (FW), supraoculars (SO), postoculars (PO), parietals (P), external skull length (ESL – distance between Points 3 and 8), and parietal suture (ParS – distance between Points 5 and 8). The numbers 1–8 in (B) represent key reference points for measurements and angles as follows: (1) anteriormost internasal contact point; (2) posteriormost internasal contact point; (3) anteriormost prefrontal contact point; (4) posteriormost prefrontal contact point and anteriormost point on the frontal; (5) point on the frontal, where the posterior edge of the frontal meets the parietal suture; (6) the two points on either side of the head where frontal, parietal, and supraocular meet; (7) the two points on either side of the head where parietal, supraocular, and postocular meet; and (8) posteriormost parietal contact point. The posterior frontal angle (PF∠) is produced by a vertex at Point 5 with rays extending from Point 5 through Point 6 on either side of the head. The anterior parietal angle (AP∠) is produced by a vertex at Point 6 and two rays, one extending from Point 6 through Point 5 and the other from Point 6 through Point 7. The ray including Points 6 and 7 is the lateral ray, and its orientation relative to the midline of the head is of diagnostic value. The yellow line in (B) shows our method of evaluating the lateral ray, which can be oriented laterally (angle of the yellow line with the midline of the head = 90° ± 10°) or posterolaterally (the angle of the red line with the midline of the head <80°). The white anterior eye line (AE) intersects the anteriormost points of the eyes and is assessed by its position in relation to the anterior frontal suture ("behind," "same level," or "in front of").

opennotspecifiedSep 2021View details →
zenodo32/100

FIGURE 6 in A new species of Stegonotus (Serpentes: Colubridae) from the remnant coastal forests of southern Timor-Leste

FIGURE 6. Dorsal head views of the paratypes of Stegonotus nancuro sp. nov., shown as both photographs and line drawings. Shown are USNM 579383 (A, A'), MCZ R-192767 (B, B'), and USNM 580550 (C, C'). The juvenile paratype (C, C') shows noticeable differences in head proportions, with eyes larger and more protruding relative to head size than in the other specimens. Scale proportions appear almost identical to those of the adults. Images not to scale.

opennotspecifiedSep 2021View details →
zenodo32/100

FIGURE 1 in A new species of Stegonotus (Serpentes: Colubridae) from the remnant coastal forests of southern Timor-Leste

FIGURE 1. Distribution of Stegonotus species in south-central Wallacea. Islands relevant to this study occupy a geographic area that stretches from some of the northern Moluccas in the northeast to Timor and Sumba Islands in the southwest. Species distribution is color-coded and islands with confirmed species records are numbered. These include S. batjanensis (encircled in yellow), found on Morotai (1), Halmahera (2), Ternate (3), Tidore (4), Kasiruta (5), Bacan (6), and Obi (7); S. modestus (green), on Seram (8), Buru (9), and Ambon (10); S. keyensis (blue), endemic to the Kei Islands (11); S. aruensis (purple), endemic to the Aru Islands (12); S. florensis (orange), endemic to Flores Island (13); S. sutteri (brown), endemic to Sumba Island (14); and S. lividus (teal), with its type locality on Semau Island (15). In the map of Timor-Leste (inset), the two localities from where S. nancuro sp. nov. is known include the type locality (red star) and a coastal forest near Betano, Samé Municipality (red circle). The globe shows the position of the depicted region relative to Australia and mainland Asia.

opennotspecifiedSep 2021View details →
zenodo32/100

FIGURE 10 in A new species of Stegonotus (Serpentes: Colubridae) from the remnant coastal forests of southern Timor-Leste

FIGURE 10. Habitat of Stegonotus nancuro sp. nov. in the Nancuro area, Manatuto Municipality, Timor-Leste. (A) Typical tropical moist forest habitat, showing a humus substrate, dense growth, and decaying logs. (B) Near the beach (the bright area at right in the image), there are few larger trees and a thick, shrubby undergrowth. (C) Access road into the Nancuro area, showing the dense vegetation and undergrowth. (D) The edge of the grassland, showing the height of the grasses against one of the expedition vehicles.

opennotspecifiedSep 2021View details →
zenodo32/100

FIGURE 3 in A new species of Stegonotus (Serpentes: Colubridae) from the remnant coastal forests of southern Timor-Leste

FIGURE 3. Head of USNM 580549, the holotype of Stegonotus nancuro sp. nov., displayed as photographs (left column) and line drawings (right column). Shown are dorsal (A, A'), right lateral (B, B'), left lateral (C, C'), and ventral (D, D') views. Scales shown in (A') include internasals (IN), prefrontals (PF), frontal (F), supraoculars (SO), and parietals (P). Scales in (B') include rostral (R), internasal (IN), prefrontal (PF), nasals (N), loreal (L), preoculars (PR), postoculars (PO), frontal (F), supraocular (SO), parietal (P), anterior temporals (AT), posterior temporals (PT), numbered supralabials (SL), mental (M), and numbered infralabials (IL). Scales in (D') include rostral (R), numbered supralabials (SL), mental (M), numbered infralabials (IL), anterior genials (AG), posterior genials (PG), gulars (G) with Roman numerals, and ventrals (V).

opennotspecifiedSep 2021View details →
ClinicalTrials.gov32/100

Food Incentives for TB Treatment Compliance in East Timor (FITTCET)

ClinicalTrials.gov study NCT00192556. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Data from: Latest Carboniferous (late Gzhelian) fusulinids from Timor Leste and their paleobiogeographic affinities

Open the record for dataset details and reuse information.

publicJan 2014View details →
zenodo28/100

Distribution. Endemic to Timor I. in Family Hipposideridae (Old World Leaf-nosed Bats)

Distribution. Endemic to Timor I.

opennotspecifiedOct 2019View details →
zenodo28/100

FIGURE 2 in Eviota santanai, a new Dwarfgoby from Timor-Leste (Teleostei: Gobiidae)

FIGURE 2. Underwater photograph of E. santanai. Photograph by M.V. Erdmann.

opennotspecifiedDec 2013View details →
zenodo28/100

FIGURE 1 in Indolestes lafaeci sp. nov. (Odonata: Lestidae) from Timor, with comparisons to related species

FIGURE 1. Lateral view of the holotype male of Indolestes lafaeci.

opennotspecifiedMar 2017View details →
zenodo28/100

FIGURE 4 in Nososticta impercepta sp. nov. (Odonata: Platycnemididae) from Timor, with a key to the Sundaic species

FIGURE 4. Nososticta impercepta wing base. Illustration: Malte Seehausen.

opennotspecifiedDec 2017View details →
zenodo28/100

Fig. 20 in Quaternary Murid Rodents Of Timor Part I: New Material Of Coryphomys Buehleri Schaub, 1937, And Description Of A Second Species Of The Genus

Fig. 20. Hypothesis of phylogenetic relationships among the major lineages of Murinae, based on the findings of recent molecular studies of multiple mitochondrial and nuclear genes (Michaux et al. 2001; Lecompte et al., 2002a, 2008; Jansa and Weksler, 2004; Jansa et al., 2006; Steppan et al., 2004; Rowe et al., 2008). Branch lengths are scaled according to the chronogram presented by Lecompte et al. (2008: fig. 2). The placement of Chiropodomys and Vandeleuria on this topology is based on the multigene phylogeny published by Rowe et al. (2008); branch lengths for these placements are approximate. The taxonomic content of each Tribe is summarized in table 3.

opencc-by-4.0Jul 2010View details →
zenodo28/100

Figs 1–7 in A new species of the Australian genus Necterosoma from Timor (Coleoptera: Dytiscidae: Hydroporini)

Figs 1–7: Necterosoma timorense sp. nov. 1 – male habitus; 2 – male protibia; 3 – median lobe in ventral view; 4 – median lobe in lateral view; 5 – right lateral lobe (paramere); 6 – female habitus in dorsal view; 7 – female habitus in ventral view. Scale bar (Figs 3–5): 0.5 mm.

opencc-by-4.0Jul 2013View details →
zenodo28/100

Distribution. Endemic to Timor I in Hipposideridae

Distribution. Endemic to Timor I

opennotspecifiedOct 2019View details →
zenodo28/100

Distribution. Endemic to Timor I. in Soricidae

Distribution. Endemic to Timor I.

opennotspecifiedJul 2018View details →
zenodo28/100

Figure 1 from: Jansen JJFJ (2017) René Maugé's ornithological collections from Kupang Bay, West-Timor, Indonesia, August-November 1801, with special regard to type-specimens. Zoosystematics and Evolution 93(2): 467-492. https://doi.org/10.3897/zse.93.19964

Figure 1 - MNHN A.C. 6490: Pedestal underside of Loxia fuscata. It shows a sticker glued. The same stickers are used on multiply specimens collected in either Australia and Timor. The handwriting is from Louis Dufresne and only used on specimens brought back with Le Naturaliste.

opencc-by-4.0Nov 2017View details →
zenodo28/100

Figure 8 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981

Figure 8 Frequency of ontogenetic stages in the subhemocoelic brood pouches of female Tarebiagranifera (Lamarck, 1816) (morph B) depending on occurrence in Thailand. Blue dots: mitochondrial clade A; pink dots: mitochondrial clade B. Size classes are assigned different colours in the pie charts (see legend) and rivers are coloured according to drainage systems; numbers at the pie charts refer to the total number of dissected specimens and the number of gravid females (in parentheses). The small letters refer to the stations Chiang Mai (a), Ko Samui (b) and Phuket (c) for which meteorological data representing the different climatic regions of Thailand were analysed (see Fig. 12).

opencc-by-4.0Nov 2018View details →
zenodo28/100

Figure 4 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981

Figure 4 Bayesiam 50% majority-rule consensus tree showing two major mitochondrial clades in Tarebiagranifera (Lamarck, 1816). Numbers at the nodes correspond to posterior probabilities (left), maximum likelihood (middle) and maximum parsimony (right) bootstrap values. At the tips of the tree voucher numbers (see material list in the main part of the text), country codes (THA: Thailand; TIM: Timor Leste; IDN: Indonesia) and the river where specimens were collected are indicated. The inset map shows the distribution of mitochondrial clades in Thailand (clade A: blue dots; clade B: magenta dots) and major river systems. The letters a–c in the map refer to localities, for which climatic data were available (see also Fig. 12). The inset with box plots shows the altitudinal distribution of mitochondrial caldes A and B, respectively.

opencc-by-4.0Nov 2018View details →
zenodo28/100

Figure 6 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981

Figure 6 Results of biometric (a–d) and geometric morphometrics study (e), for four different morphs (A,B,C,Timor) of Tarebiagranifera (Lamarck, 1816). Boxplots of (a) shell height, (b) shell width, (c) height of the last three whorls and (d) index of height of last three whorls agaianst shell width. Significant differences between groups are indicated by bars above the boxplots (e) Relative variance in shell shape along PC1 and PC2. Colour corresponding planes indicate the spread of each morph in the data set.

opencc-by-4.0Nov 2018View details →

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