We describe a new species of the genus Ninia from the Chocó-Magdalena biogeographic province, which was previously reported as a distinct population of N. maculata or as N. atrata from the western slopes of the Cordillera Occidental of Colombia. The new species is similar to N. atrata, N. celata, N. espinali, N. franciscoi, and N. maculata. It shares the following characteristics with the species mentioned above: 19 dorsal scale rows without reductions; dorsal ground color black or dark brown; white or cream occipital nuchal collar. However, it is easily distinguished from all other congeners because it has a non-regular color pattern in the ventral surfaces of the head and body, subcaudal surface homogeneously black or dark brown, two nasal scales, and one lateral projection ornamented with a large basal hook-shaped spine that is larger than any other spine on the hemipenial body. The presence of a lateral projection on the hemipenial body makes the new species the only member of the genus from South America that shares this feature with its Central American congeners. This feature suggests a closer relationship with this linage. Finally, our results indicate that proper and careful revision of the Ninia atrata species complex will help to understand and clarify the taxonomic composition of the genus.
Keywords: Reptilia, External morphology, Biogeography of the Colombian Pacific lowlands, Hemipenis, Ninia atrata, Ninia maculata, taxonomy
Ninia teresitae sp. nov.
FIGURE 2. General view of the holotype (ICN 12527) of Ninia teresitae sp. nov., in life (A), dorsal (B) and ventral (C) views after its preservation.
Etymology. The specific epithet teresitae represent the Latin translation of the nickname from the Spanish “Teresita” and is given in honor to the grandmother of the first author, Maria Teresa Guerrero (1915−2013). “Teresita” was one of the most influential persons in her grandson’s life, who never failed to support him and encouraged his endless passion for snakes.
Teddy Angarita-Sierra and John D. Lynch. 2017. A New Species of Ninia (Serpentes: Dipsadidae) from Chocó-Magdalena Biogeographical Province, western Colombia. Zootaxa. 4244(4); 478–492. DOI: 10.11646/zootaxa.4244.4.2
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شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
The genus Dendropsophus is one of the most speciose among Neotropical anurans and its number of described species is increasing. Herein, molecular, morphological, and bioacoustic evidence are combined to assess species limits within D. parviceps, a widely distributed species in the Amazon Basin. Phylogenetic relationships were assessed using 3040 bp sequences of mitochondrial DNA, genes 12S, ND1, and CO1. The phylogeny shows three well-supported clades. Bioacoustic and morphological divergence is congruent with those clades demonstrating that Dendropsophus parviceps is a species complex. Dendropsophus parviceps sensu stricto occurs in the Amazon basin of Ecuador, northern Peru, southern Colombia and northwestern Brazil. It is sister to two previously undescribed species,Dendropsophus kubricki sp. n. from central Peru and Dendropsophus kamagarini sp. n. from southern Peru, northeastern Bolivia, and northwestern Brazil. Genetic distances (uncorrected p, gene 12S) between D. parviceps and the new species is 3 to 4%. Dendropsophus kamagarini sp. n. can be distinguished from D. parviceps by having a prominent conical tubercle on the distal edge of the upper eyelid (tubercle absent in D. parviceps). Dendropsophus kubricki sp. n. differs from D. parviceps by having scattered low tubercles on the upper eyelids (smooth in D. parviceps). Dendropsophus parviceps and both new species differ from all their congeners by their small size (adult maximum SVL = 28.39 mm in females, 22.73 mm in males) and by having a bright orange blotch on the hidden areas of the shanks and under arms. The advertisement call of the two new species has lower dominant frequency relative to D. parviceps. Probable speciation modes are discussed. Available evidence indicates that ecological speciation along an elevation gradient is unlikely in this species complex.
Figure 6. Dorsolateral and ventral views of Dendropsophus parviceps in life: A, B Adult male, from type locality Sarayaku, Pastaza, Ecuador (QCAZ 52752) C, D Adult male, from Canelos, Pastaza, Ecuador (QCAZ 52816) E Adult male, from Yasuní, Orellana, Ecuador (QCAZ 51073) F Amplectant pair from Nuevo Rocafuerte, Río Napo, Orellana, Ecuador (QCAZ 44773–74) G, H Adult female, from Chiroisla, Río Napo, Orellana, Ecuador (QCAZ 44440). Photographs by S. Ron.
Figure 1. Bayesian consensus phylogeny of Dendropsophus parviceps species complex based on 3040 bp of mtDNA. Node support is indicated with Bayesian posterior probabilities (pp) above branches and non-parametric bootstrap support below. Asteriks denote nodes with pp = 1 and bootstrap values = 100%. Outgroups, bootstrap values < 60%, and pp < 0.8 are not shown. Museum number and locality are provided for each sample. Abbreviations: BR = Brazil, PE = Peru, and EC = Ecuador.
Figure 9. Distribution of Dendropsophus parviceps species complex. Dendropsophus parviceps (Northern Clade, blue crosses), D. kubricki sp. n. (Central Clade, green circles), D. kamagarini sp. n. (Southern Clade, orange rhombi). Stars = type locality, figures with a small black dot at the center = referred specimens, and hollow figures = unconfirmed records.
Dendropsophus parviceps (Boulenger, 1882)
Hyla parviceps Boulenger, 1882: 393. Holotype BMNH 1947.2.13.51, an adult female from “Sarayacu”, Pastaza Province, Ecuador.
Dendropsophus parviceps – Faivovich et al. 2005: 93.
Diagnosis: Throughout the species account, coloration refers to preserved specimens unless otherwise noted. Dendropsophus parviceps is characterized by: (1) small size, mean SVL 16.4 mm in males (range 14.3–18.7; n = 65), 22.5 mm in females (range 20.3–24.4; n = 30); (2) throat sexually dimorphic, dark flecks posteriorly in males vs. white blotch with two or three longitudinal stripes or without stripes posteriorly in females (Fig. 8); (3) snout truncate in dorsal and lateral views, slightly inclined posteroventrally in lateral view; (4) nostrils slightly prominent; (5) tympanum visible, concealed posterodorsally, tympanic membrane differentiated and annulus evident; (6) conical tubercles on upper eyelid absent; (7) thoracic fold absent; (8) ulnar tubercles and outer tarsal tubercles indistinct; (9) axillary membrane present; (10) skin on dorsal surfaces smooth with scattered small tubercles; skin on chest areolate; skin on belly, posterior surfaces of thighs, and subcloacal area coarsely areolate; skin on throat and other surfaces smooth; (11) dark brown markings on dorsum (Fig. 8); (12) thenar tubercle is distinct; (13) hand webbing formula II11/2–2III2-–2-IV, feet webbing formula I1-−2-II1-−2-III1-–2IV2−1-V; (14) in life, dorsal surfaces brown, tan or grayish tan; (15) orange to amber blotch on the proximal ventral surface of shanks and under arms, from the axillae to near the elbow, in life (white to creamy white in preservative); (16) one suborbital white bar present both in life and preservative; (17) thighs are black to dark brown with two or three white spots on the anterodorsal surfaces both in life and preservative; (18) iris in life is creamy white to reddish brown with brow or dark brown reticulations.
.....
Distribution and ecology: Dendropsophus parviceps is known from 39 localities in the Ecuadorian Amazon basin (Napo, Orellana, Pastaza, Sucumbíos, and Tungurahua provinces; Fig. 9), few localities in the Peruvian Amazon basin at northwest Loreto (Andoas and San Jacinto; Fig. 9), the Colombian Amazon (Río Apaporis, Vaupés Department, and Ceilán, Caquetá Department; Cochran and Goin 1970; Fig. 9), and northern Brazil (“Taracuá” [= Taracuacá], Río Uaupés, Amazonas State; Melin 1941). Elevation range is 151 m (Andoas) to 1600 m above sea level (Río Verde). Our Colombian records are unverified and are based on Cochran and Goin (1970) who examined three specimens (MLS 54 and MCZ 28058–59) and explicitly mention the absence of tubercles on the upper eyelids. Moreover, the SVL for a gravid female from Ceilan (MLS 54, 21.8 mm) falls outside the known size range of D. kubricki sp. n. and D. kamagarini sp. n. (Table 3). Ecuadorian localities from Sucumbíos province are close to the Colombian border further suggesting the presence of D. parviceps in Colombia. In addition, there is an unconfirmed register of D. parviceps from Ramal do Purupuru, km 34 on the BR-319 highway (3.3535°S, 59.8557°W, 35 m, Amazonas State, Brazil; Fig. 9).
Dendropsophus parviceps inhabits Amazonian lower montane forest, Amazonian foothill forest, and Amazonian evergreen lowland rainforest (habitat types based on Ron et al. 2017). Dendropsophus parviceps is an opportunistic breeder and can be found in primary and secondary forest, temporary ponds, flooded areas, swamps, and artificial open areas. Calling activity starts at dusk (17–18h), but it is mainly nocturnal. According to Lynch (2005), D. parviceps is a canopy species that visits the lower forest strata for breeding.
Figure 10. Dorsolateral and ventral views ofDendropsophus kamagarini sp. n. in life: A, B Adult male, from La Habana, Tambopata, Peru (CORBIDI 5259) C, D Adult male, from Bahuaja, Puno, Peru (CORBIDI 13148) E–H Adult females, from Pagoreni norte, La Convención, Peru E, F not collected. Dorsolateral and ventral views of Dendropsophus kamagarini sp. n. in life: G, H (CORBIDI 10018) I, J Adult male, from Tahuamanu, Nicolás Suárez, Bolivia (11.4074°S, 69.0180°W, 260 m, not collected) K, L Adult male, from El Negro, Manuripi, Bolivia (12.3134°S, 68.6689°W, 187 m, not collected) N Adult male, from Rio Branco, Acre, Brazil (10.0387°S, 67.7957°W, 160 m, not collected) M Adult male, from Rio Madeira, Rondônia, Brazil (8.8482°S, 64.0689°W, 110 m, not collected). Photos A, B, E–H by V. Duran, C, D by P. J. Venegas I–L by A. Muñoz, N by P.R. Melo-Sampaio, and M by A.P. Lima.
Dendropsophus kamagarini sp. n.
Etymology: The specific name kamagarini is a noun derived from the Matsigenka language, which means demon or devil (Snell et al. 2011). The Matsigenka language is spoken by the Matsigenka people who inhabit the highlands and lowlands of southeastern Peru, in the departments of Cusco and Madre de Dios. Judeo-Christian religions depict the demon as a human figure with horns. The species name is in allusion to the prominent horn-like tubercles on the upper eyelid of D. kamagarini.
Diagnosis: Throughout the species description, coloration refers to preserved specimens unless otherwise noted. The new species is assigned to the genus Dendropsophus based on our phylogenetic results (Fig. 1) and the overall similarity with D. parviceps and other species of the genus (Figs 10–11). Dendropsophus kamagarini is a medium-sized species, relative to other species in the D. parviceps group and is characterized by the following combination of traits: (1) size sexually dimorphic; mean SVL 19.9 mm in males (range 17.6–22.7; n = 35), 26.1 mm in females (range 24.0–28.1; n = 7); (2) throat brown mottled with white flecks posteriorly in males vs. white blotch with flecks or with stripes posteriorly in females (Fig. 11); (3) snout is short and truncate in dorsal and lateral views; (4) nostrils slightly protuberant; (5) tympanum visible, tympanic membrane non-differentiated, annulus distinct; (6) one prominent conical tubercle on the distal edge of the upper eyelid; (7) thoracic fold indistinct to barely evident; (8) ulnar tubercles and outer tarsal tubercles distinct; (9) axillary membrane present; (10) skin on dorsal surfaces smooth with scattered tubercles; skin on chest, belly, posterior surfaces of thighs, and subcloacal area coarsely areolate; skin on throat grooved with scattered tubercles; (11) dark brown markings on dorsum (Fig. 11); (12) thenar tubercle distinct; (13) hand webbing formula II1-–2+III1-–1-IV, feet webbing formula I11/2–2+II1-–1III1-–2-IV2–1V; (14) in life, dorsum tan, brown or reddish brown; (15) orange to amber blotch on the proximal ventral surface of shanks and under arms, from the axillae to near the elbow, in life (white to creamy white in preserved); (16) one suborbital white bar present both in life and preserved; (17) thighs black to dark brown with two or three spots on the anterodorsal surfaces both in life and preserved; (18) iris in life creamy white with brown to reddish brown reticulations and a cream ring around pupil.
Distribution and ecology: Dendropsophus kamagarini occurs in the Amazon basin of southeastern Peru (Cusco and Madre de Dios regions; Fig. 9), northwestern Brazil (Acre and Rondônia states; Fig. 9), and northeastern Bolivia, from the Andean slopes to lowland tropical rainforest (Fig. 9). Localities with known elevation range from 150 m (Acre) to 1696 m (Ochigoteni) above sea level.
Figure 13. Dorsolateral and ventral views of Dendropsophus kubricki sp. n. in life: A, B Holotype, adult male, from Río Tapiche, Requena, Peru (CORBIDI 15778) C, D Adult male from Río Tapiche, Requena, Peru (CORBIDI 15782) E Adult male from Jenaro Herrera, Requena, Peru (not collected) F Adults, pair in amplexus from Jenaro Herrera, Requena, Peru (not collected).Dorsolateral and ventral views of Dendropsophus kubricki sp. n. in life: G, H Adult female from Jenaro Herrera, Requena, Peru (not collected) I, J Adult female from Area de Conservación Municipal Chambira, Picota, Peru (CORBIDI 8864) K Adult female from Tarapoto, San Martín, Peru (6.4306°S, 76.2903°W, 600 m, not collected) L Adults, pair in amplexus from Area de Conservación Municipal Chambira, Picota, Peru (CORBIDI 8864–63). Photographs by P. J. Venegas.
Dendropsophus kubricki sp. n.
Etymology: The specific name kubricki is a noun in the genitive case and is a patronym for Stanley Kubrick, an American filmmaker who is one of the most brilliant and influential film directors of all time. We dedicate this species to him for his legacy to film culture and science fiction.
Diagnosis: Throughout the species description, coloration refers to preserved specimens unless otherwise noted. The new species is assigned to the genus Dendropsophus based on our phylogenetic results (Fig. 1) and the overall similarity with D. parviceps and other species of the genus (Figs 13–14). Dendropsophus kubricki is a medium-sized species, relative to other species in the D. parviceps group and is characterized by the following combination of traits: (1) size sexually dimorphic; mean SVL 19.4 mm in males (range 18.3–20.1; n = 14), 26.0 mm in females (range 22.0–28.4; n = 8); (2) throat with white flecks posteriorly in males and white blotch with stripes posteriorly in females (Fig. 14); (3) snout truncate in dorsal view, rounded and inclined posteroventrally in lateral view; (4) nostrils slightly prominent; (5) tympanum distinct, rounded, concealed posterodorsally, tympanic membrane non-differentiated and annulus evident; (6) low tubercles on upper eyelid can be distinct or ill-defined; (7) thoracic fold slightly evident or indistinct; (8) ulnar tubercles and outer tarsal tubercles low; (9) axillary membrane present; (10) skin on dorsal surfaces smooth with scattered tubercles mainly on head; skin on throat areolate, skin on chest, belly, posterior surfaces of thighs, and subcloacal area coarsely areolate; (11) dark brown markings on dorsum consisting of chevrons and transverse blotches in variable arrangements (Fig. 14); (12) thenar tubercle distinct; (13) hand webbing formula II1-−2+III1-−1-IV, foot webbing formula I1-−2-II1-−2-III1-–2IV2−1-V; (14) in life, dorsal surfaces reddish brown, brown, or grayish tan; (15) orange to amber blotch on the proximal ventral surface of shanks and under arms, from the axillae to near elbow, in life (white to creamy white in preserved); (16) one suborbital white bar present both in life and preserved; (17) anterodorsal surfaces of thighs are black to dark brown with two or three white spots, both in life and preserved; (18) iris in life is reddish brown, brown or silver gray.
Distribution and ecology: Dendropsophus kubricki is distributed in the Amazon basin in northeastern and central Peru (Fig. 9), at elevations between 106 (Jenaro Herrera) and 725 m (Cordillera Azul). Dendropsophus kubricki was found in flooded forest. Specimens from Chambira were collected in a small pond in a Terra Firme forest. Males call at night while perching on leaves of bushes and trees. They were observed between 0.3 and 0.4 m above the water.
C. Daniel Rivadeneira, Pablo J. Venegas and Santiago R. Ron. 2018. Species Limits within the Widespread Amazonian treefrog Dendropsophus parviceps with Descriptions of Two New Species (Anura, Hylidae). ZooKeys. 726; 25-77. DOI: 10.3897/zookeys.726.13864
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
• The family Salamandridae is of Western Palearctic origin and started to diversify in the Late Cretaceous.
• The common ancestor was oviparous, mated on land without amplexus and probably showed a pin wheel spermatophore transfer.
• Colonization took place once to the Nearctic and twice to Eastern Asian realms.
• Changes in habitat type are not significantly correlated with changes in mating characters.
Abstract
Amphibians have a complex reproductive behaviour, which shows the highest diversity among tetrapodes. The family Salamandridae, distributed across the entire Holarctic, is one of the most diverse groups of extant salamanders comprising 114 species in 21 genera. The family has a remarkable diversity of courtship modes, amplexus and sperm transfer. It is often hypothesised that this diversity has evolved in adaptation to a specific mating and/or breeding habitat. We test this hypothesis based upon a phylogenetic reconstruction using the complete mitochondrial genome sequences of 45 Salamandridae species, representing all existing genera. We used ancestral character state reconstruction methods and geographic range models and applied relaxed Bayesian molecular clock models to discuss the results in a temporal framework of Salamandridae evolution. Our results show that the family Salamandridae started to diversify in the Late Cretaceous (ca. 87 mya) and is of Western Palearctic origin. Ancestral character state reconstruction predicts that its common ancestor was oviparous, mated on land without amplexus and probably showed a pin wheel spermatophore transfer, which is still found in the Italian endemic Salamandrina terdigidata. Our results suggest that several colonization of continents with subsequent radiations took place, once to the Nearctic and twice into Eastern Asian realms. However, these events were only in one case associated with a change in mating behaviour (dorsal amplexus in Nearctic newts). Around the Cretaceous-Paleogene boundary (K-Pg boundary) several Salamandridae lineages further diverged, again with no obvious changes in mating behaviour. Overall, there is no significant signal for mating character evolution being caused by changes in habitat type, with only a slight tendency that changes in mating habitat might have led to changes in the type of sperm transfer which in turn was associated with changes in the presence or absence of amplexus.
Keywords: Mitogenomics; Bayesian molecular dating; geographic range; mating behaviour; ancestral character state reconstruction; coevolution
Sarah Kieren, Max Sparreboom, Axel Hochkirch and Michael Veith. 2018. A Biogeographic and Ecological Perspective to the Evolution of Reproductive Behaviour in the Family Salamandridae. Molecular Phylogenetics and Evolution. In Press. DOI: 10.1016/j.ympev.2018.01.006
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
An increase in ecological opportunities, either through changes in the environment or acquisition of new traits, is frequently associated with an increase in species and morphological diversification. However, it is possible that certain ecological settings might prevent lineages from diversifying. Arboreality evolved multiple times in vipers, making them ideal organisms for exploring how potentially new ecological opportunities affect their morphology and speciation regimes. Arboreal snakes are frequently suggested to have a very specialized morphology, and being too large, too small, too heavy, or having short tails might be challenging for them. Using trait-evolution models, we show that arboreal vipers are evolving towards intermediate body sizes, with longer tails and more slender bodies than terrestrial vipers. Arboreality strongly constrains body size and circumference evolution in vipers, while terrestrial lineages are evolving towards a broader range of morphological variants. Trait-dependent diversification models, however, suggest similar speciation rates between microhabitats. Thus, we show that arboreality might constrain morphological evolution but not necessarily affect the rates at which lineages generate new species.
The arboreal Stejneger's Pitviper (Trimeresurus stejnegeri).
Photo: M. Martins
Laura Rodrigues Vieira de Alencar, Marcio Martins, Gustavo Burin and Tiago Bosisio Quental. 2017. Arboreality Constrains Morphological Evolution but Not Species Diversification in Vipers. Proceedings of the Royal Society B: Biological Sciences. 284(1869)DOI: 10.1098/rspb.2017.1775
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
We describe a new species of Rhacophorus based on two adult specimens collected from Hoa Binh Province, northern Vietnam. Rhacophorus hoabinhensis sp. nov. is distinguishable from its congeners on the basis of a combination of the following morphological characters: size small (SVL 31.1–32.5 mm in males); head slightly longer than wide; vomerine teeth absent; snout short (SNL/SVL 0.16); dorsal skin smooth; forearm and tarsus with dermal fringes; dermal appendage at vent present; webbing formula on fingers I12/3-12/3II1-2III1-1IV and on toes I3/4-1II1/2- 1III1/2-1IV1-1/2V; dorsal surface grey yellow with brown spots; lower jaw region dark grey, throat, chest and belly cream; anterior and posterior thighs, as well as ventral surface of tibia orange. The interspecific uncorrected genetic distances (16S rRNA gene) between the new species from Hoa Binh and other analyzed congeners varied from 9.8% to 17.4%. In the phylogenetic analyses, the new species revealed to be a representative of Rhacophorus and was nested within the R. hoanglienensis-orlovi species group.
Keywords:Rhacophorus hoabinhensis sp. nov., karst forest, molecular phylogeny, taxonomy, Hoa Binh Province
Figure 2 Dorsal and ventral views of the adult male holotype (IEBR A.2016.18) ofRhacophorus hoabinhensis sp. nov. from Hoa Binh Province, northern Vietnam.
Figure 4 Rhacophorushoabinhensis sp. nov. in its biotope in Hang Kia–Pa Co Nature Reserve, Hoa Binh Province, Vietnam.
Rhacophorus hoabinhensis sp. nov.
Etymology: The specific epithet “hoabinhensis” refers to the type locality of the new species, Hoa Binh Province. For the common names we suggest Hoa Binh Treefrog(English), and Ếch cây hòa bình (Vietnamese).
Distribution:R. hoabinhensis is currently is known only from the type locality in Hang Kia–Pa Co Nature Reserve, Hoa Binh Province, Vietnam.
Natural history:Rhacophorus hoabinhensis appears to be closely associated with karstic environment. Specimens were found at night between 19:00 and 23:30h, near a small pond. The surrounding habitat was secondary karst forest, consisting of medium and small hardwoods mixed with shrubs and vines. Specimens were found on leaves and branches of trees, about 1.2–1.5 m above the ground. The advertisement call of the species was not heard. The air temperatures at the times of collection ranged from 14.8 to 18.9o C and relative humidity from 84% to 93%. Other rhacophorid species recorded in Hang Kia–Pa Co Nature Reserve were Raorchestes parvulus Boulenger, R. feaeBoulenger, R. kio Ohler and Delorme, R. orloviZiegler and Köhler, Theloderma albopunctatumLiu and Hu, T. gordoniTaylor, and T. lateriticum Bain, Nguyen and Doan. Females and the tadpole of Rhacophorus hoabinhensis have not been recorded so far.
Tao Thien Nguyen, Cuong The Pham, Truong Quang Nguyen, Hoa Thi Ninh and Thomas Ziegler. 2017. A New Species of Rhacophorus (Amphibia: Anura: Rhacophoridae) from Vietnam. Asian Herpetological Research.8(4); 221–234. DOI: 10.16373/j.cnki.ahr.170046
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
We collected two specimens of an undescribed species of Lygosoma from pitfall traps in an urban rainforest in Kuching and from the base of a forested hill in western Sarawak, East Malaysia. The new species is diagnosable from all south-east Asian congeners by morphological characters, and most closely resembles Lygosoma herberti from the Thai-Malay Peninsula. The new species shows substantial molecular divergence from its closest relatives in two protein-coding genes, one mitochondrial (ND1) and one nuclear (R35) that we sequenced for several south-east Asian congeners. We describe the new species on the basis of this distinct morphology and genetic divergence. It is the third species of Lygosoma known from Borneo, and highlights the continuing rise in lizard species diversity on the island. In addition, the discovery of this species from a small urban rainforest underscores the importance of preserving intact rainforest areas of any size in maintaining species diversity.
Keywords: Reptilia, Borneo; Sarawak; Scincidae; Lygosoma samajaya new species
FIGURE 3. Photo in life of the holotype of Lygosoma samajaya sp. nov.
Lygosoma samajaya sp. nov. Etymology. The species epithet samajaya is a proper noun in apposition that refers to the locality of collection of the holotype at the Sama Jaya Forest Reserve in Kuching, Sarawak, Malaysia. This name draws attention to the importance of small urban rainforest parks in sustaining species diversity.
Benjamin R. Karin, Elyse S. Freitas, Samuel Shonleben, L. Lee Grismer, Aaron M. Bauer and Indraneil Das. 2018. Unrealized Diversity in An Urban Rainforest: A New Species of Lygosoma (Squamata: Scincidae) from western Sarawak, Malaysia (Borneo). Zootaxa. 4370(4); 345–362. DOI: 10.11646/zootaxa.4370.4.2
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
Integrative taxonomy seeks to approach the complex topic of species diagnosis using independent, complementary lines of evidence. Despite their ubiquity throughout North and Central America, taxonomy of the American leopard frogs (Anura: Ranidae: Rana: subgenus Pantherana) remains largely unresolved, and this is arguably nowhere truer than in the Central American country of Honduras, where there are two nominal species, the taxonomy of which remains unresolved. Leopard frogs from several mountainous areas along the continental divide in Honduras have previously been considered putative hybrids between Rana brownorum and R. cf. forreri, as opposed to two alternate hypotheses: one that they represent a high-altitude eco-morph of a single widespread species that included both lowland forms, or a second that there is an undescribed highland species distinct from either of the recognized lowland forms. We examine this set of hypotheses using three independent lines of evidence. First, we used species distribution modelling to examine potential geographic isolation of the highland form and the two putative parental lowland species, and found strong ecological separation between the highland and lowland forms. Second, mitochondrial and nuclear DNA supports the distinction of the highland form from both putative parental species, with mtDNA data refuting the hypothesis that representatives of either species may represent a matrilineal founder. Morphologically, the highland form is significantly smaller than, and otherwise readily differentiated from, both R. brownorum and R. cf. forreri, as well as all other Rana found in Honduras and adjacent areas. As a result, we formally describe the highland leopard frog as a new species.
Key words: Amphibia, integrative taxonomy, mitochondrial DNA, Pantherana, phylogeny, rhodopsin, species distribution modelling
Rana lenca sp. nov.
Common English name. Lenca Leopard Frog
Common Spanish name. La Rana Lenca
Etymology. The name lenca is given in honour of the indigenous Lenca people, the traditional inhabitants of the mountainous region of south-western Honduras.
Paratypes of Rana lenca from Reserva Biologica Cerro Uyuca, 1,640 m elevation, Departamento de Francisco Morazan,Honduras: (1) adult female paratype (UF 166642; 64.3 mm SL); (2) Subadult female paratype (UF 166643) and tadpole (UF 166637).
Photos by Jason M. Butler.
Unvouchered examples of Rana lenca; (1) adult male from the type locality; (2) adult female from the type locality; (3) adult male from the Reserva Biologica Cerro Uyuca; (4) adult female from the Reserva Biologica Cerro Uyuca.
Unvouchered examples of Rana lenca; (1) adult male from the type locality; (2) adult female from the type locality; (3) adult male from the Reserva Biologica Cerro Uyuca; (4) adult female from the Reserva Biologica Cerro Uyuca; (5) adult male at edge of pond at type locality; (6) adult female floating amongst Pinus oocarpa needles in a spring-fed pool at Reserva Biologica Cerro Uyuca.
Type locality of Rana lenca; San Pedro La Loma, 2010 m elevation, Depto. Intibuca, Honduras. in January 2008 (top) and during drought conditions in May 2015 (bottom).
Ileana Luque-Montes, James D. Austin, Kayla D. Weinfurther, Larry David Wilson, Erich P. Hofmann and Josiah H. Townsend. 2018. An Integrative Assessment of the Taxonomic Status of Putative Hybrid Leopard Frogs (Anura: Ranidae) from the Chortís Highlands of Central America, with Description of A New Species. Systematics and Biodiversity. In Press. DOI 10.1080/14772000.2017.1415232
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
