The avifauna of Rote Island in the Lesser Sundas is not well studied and generally considered to be similar to that of adjacent Timor Island. However, some cases of bird endemism have recently been documented on this island. A population of Myzomela honeyeater is one such example. First observed in October 1990, it has been subsumed with Myzomela dammermani from Sumba Island given its superficially similar appearance. Based on extensive morphological inspection and bioacoustic analysis, we here describe this population as a new taxon to science. Apart from previously overlooked plumage distinctions, the new taxon bioacoustically differs from M. dammermani in the presence or absence of several unique call types and considerable differences across two parameters in shared call types. Considering the importance of bioacoustics in avian species delimitation, we propose that the new Rote Myzomela be considered a distinct species. Given continued habitat conversion across its small range, we propose the International Union for Conservation of Nature and Natural Resources (IUCN) threat status Vulnerable for the species.
Key words: bird, Lesser Sundas, Myzomela, new species, Rote Island
Male ‘Rote Myzomela’ Myzomela irianawidodoae sp. nov., near Bolatena village, Rote Island, East Nusa Tenggara Province, Indonesia, April 2014.
Figure 1. Map showing distribution of a select group of Myzomela taxa with a similar morphology. A – Sumba Myzomela M. dammermani (Sumba Island; turquoise), B – the newly-described Rote Myzomela [Myzomela irianawidodoae] (Rote Island; red), C – Timor Myzomela M. vulnerata (Timor Island; dark blue), D – Banda Myzomela M. boiei (Banda Island arc and Tanimbar Islands; pink), E –Red-headed Myzomela M. erythrocephala (coastal Australia and Papua, Aru Islands; yellow).
Myzomela irianawidodoae, species nova English name: Rote Myzomela Indonesian name: Myzomela Rote Etymology: We are pleased to name this species after Iriana Widodo, the current First Lady of the Republic of Indonesia, to recognise her keen interest in Indonesia’s birdlife and her valuable stewardship and advocacy for Indonesia’s natural environments.
....
Dewi Malia Prawiradilaga, Pratibha Baveja, Suparno, Hidayat Ashari, Nathaniel Sheng Rong Ng, Chyi Yin Gwee, Philippe Verbelen and Frank Erwin Rheindt. 2017. A Colourful New Species of Myzomela Honeyeater from Rote Island in eastern Indonesia. Treubia. 44; 77-100. http://e-journal.biologi.lipi.go.id/index.php/treubia/article/view/3414
The discovery of Myzomela irianawidodoae — named after Indonesia’s first lady, Iriana Joko Widodo — involved a series of separate field studies between 1990 and 2015 by different groups of researchers, according to a paper published Dec. 31, 2017, in the scientific journal Treubia.
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.
A new species of amblycipitid catfish is here described from the Indawgyi Lake basin of the Irrawaddy River drainage in Kachin State, Myanmar as Amblyceps improcerum, new species. It can be distinguished from congeners in having a unique combination of the following characters: lower jaw longer than upper; head length 17.4–22.3% SL; head width 13.7–15.2% SL; head depth 9.0–11.7% SL; interorbital distance 31–39% HL; eye diameter 7–10% HL; 37–38 vertebrae; lateral line incomplete; predorsal length 25.5–30.7% SL; smooth posterior margin of pectoral spine; pectoral-fin length 13.5–16.8% SL; pelvic-fin length 9.6–13.4% SL; dorsal-to-adipose distance 25.2–28.7% SL; length of adipose-fin base 19.4–23.3% SL; adipose fin separate from dorsal procurrent caudal-fin rays; preanal length 62.1–66.9% SL; body depth at anus 9.8–12.8% SL; depth of caudal peduncle 10.1–12.6% SL; length of caudal peduncle 21.4–24.0% SL, post-adipose distance 15.8–17.8% SL; weakly-forked caudal fin with short broadly, rounded lobes (length of longest ray 1.3–1.5 times length of median rays); centrally projecting hooks on proximal lepidotrichia of median caudal-fin rays absent.
Keywords: Ostariophysi, Sisoroidea, Irrawaddy river, New species
Fig. 1 Amblyceps improcerum, holotype, MHNG 2768.061, 53.2 mm SL; Myanmar: Kachin State: Lake Indawgyi basin. Dorsal, lateral and ventral views
Amblyceps improcerum, new species
Etymology: The specific epithet comes from the Latin adjective improcerus, −a, −um, meaning "not tall" or "undersized", in reference to the relatively short caudalfin lobes and adipose-fin base of this species when compared to nearly all congeners.
Heok Hee Ng and Maurice Kottelat. 2018. Amblyceps improcerum, A New Sisoroid Catfish from Kachin State, Myanmar (Teleostei: Siluriformes: Amblycipitidae). Environmental Biology of Fishes. DOI: 10.1007/s10641-017-0712-0
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 Desmatophocidae represents an early radiation of extinct pinnipeds that peaked in diversity during the middle Miocene. Although represented by abundant well-preserved fossils, the taxonomy and evolutionary relationships of this family remain poorly known. Late Miocene desmatophocids have been recorded, although none have been formally described, preventing a thorough appraisal of their decline and extinction. We report the discovery of a new species, Allodesmus demerei sp. nov., represented by a partial skeleton with cranium, mandibles, and axial skeleton, from the upper Miocene Montesano Formation of Washington, prompting reinterpretation of desmatophocid taxonomy, phylogeny, and extinction. Phylogenetic analysis (95 characters, 26 taxa) found strong support for monophyletic Desmatophocidae and Allodesmus. Desmatophocidae was found as sister to Phocidae with poor support. Allodesmus demerei was placed within the Allodesmus as the sister taxon to Allodesmus kernensis. The geochronologically young age (10.5–9.1 Mya) of Al. demerei establishes this species as the last of the desmatophocid seals. The middle Miocene peak in desmatophocid diversity coincides with the middle Miocene climatic optimum, suggesting that declining sea surface temperature played a role in their decline and extinction. Walruses diversified and increased in body size during the mid- to late Miocene as desmatophocids declined, suggesting some form of ecological displacement.
Robert W. Boessenecker and Morgan Churchill. 2018. The Last of the Desmatophocid Seals: A New Species of Allodesmus from the upper Miocene of Washington, USA, and a revision of the taxonomy of Desmatophocidae. Zoological Journal of the Linnean Society. zlx098. DOI: 10.1093/zoolinnean/zlx098
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.
Figure 1. The four main groups of myriapods. A, Otostigmus (Parotostigmus) pococki (Northern Range, Trinidad, Trinidad and Tobago) (Chilopoda, Scolopendromorpha); B, Hanseniella sp. (South Island, New Zealand) (Symphyla, Scutigerellidae); C, Pauropus huxleyi (Massachusetts, USA) (Pauropoda, Tetramerocerata); and D, Platydesmus sp. (La Selva, Costa Rica) (Diplopoda, Platydesmida).
The interrelationships of the four classes of Myriapoda have been an unresolved question in arthropod phylogenetics and an example of conflict between morphology and molecules. Morphology and development provide compelling support for Diplopoda (millipedes) and Pauropoda being closest relatives, and moderate support for Symphyla being more closely related to the diplopod-pauropod group than any of them are to Chilopoda (centipedes). In contrast, several molecular datasets have contradicted the Diplopoda–Pauropoda grouping (named Dignatha), often recovering a Symphyla–Pauropoda group (named Edafopoda). Here we present the first transcriptomic data including a pauropod and both families of symphylans, allowing myriapod interrelationships to be inferred from phylogenomic data from representatives of all main lineages. Phylogenomic analyses consistently recovered Dignatha with strong support. Taxon removal experiments identified outgroup choice as a critical factor affecting myriapod interrelationships. Diversification of millipedes in the Ordovician and centipedes in the Silurian closely approximates fossil evidence whereas the deeper nodes of the myriapod tree date to various depths in the Cambrian-Early Ordovician, roughly coinciding with recent estimates of terrestrialisation in other arthropod lineages, including hexapods and arachnids.
Figure 2A. Preferred phylogenetic hypothesis of myriapod interrelationships (PhyloBayes, matrix 1). 2B. DensiTree visualization of the four most congruent analyseis (PhyloBayes, matrices 2 and 3; PhyML, matrix 3). 2C, 2D. Main conflicting alternative hypothesis (2C, PhyML, matrix 2; 2D, PhyML, matrix 1). 2E. Phylogenetic hypothesis of Myriapoda based on 232 morphological characters coded for both extant and extinct species (see Methods for further details); strict consensus of 488 trees of 257 steps; Fossil taxa are identified with a dagger symbol. Black circles in nodes represent high support (> 95% posterior probability, > 90% bootstrap support). CHE: Chelicerata. PAN: Pancrustacea. CHI: Chilopoda. SYM: Symphyla. PAU: Pauropoda. DIP: Diplopoda. Colour codes for each clade are maintained in all figures.
Figure 1. The four main groups of myriapods. A, Otostigmus (Parotostigmus) pococki (Northern Range, Trinidad, Trinidad and Tobago) (Chilopoda, Scolopendromorpha); B, Hanseniella sp. (South Island, New Zealand) (Symphyla, Scutigerellidae); C, Pauropus huxleyi (Massachusetts, USA) (Pauropoda, Tetramerocerata); and D, Platydesmus sp. (La Selva, Costa Rica) (Diplopoda, Platydesmida).
Rosa Fernández, Gregory D. Edgecombe and Gonzalo Giribet. 2018. Phylogenomics Illuminates the Backbone of the Myriapoda Tree of Life and Reconciles Morphological and Molecular Phylogenies. Scientific Reports. 8, 83. DOI: 10.1038/s41598-017-18562-w
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 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
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 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.
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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
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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.
