Showing posts with label Acoustics. Show all posts
Showing posts with label Acoustics. Show all posts

Friday, June 28, 2024

[Ornithology • 2024] Caprimulgus ritae • A New Species of Nightjar (Caprimulgiformes: Caprimulgidae) from Timor and Wetar, Lesser Sunda Islands, Wallacea


Caprimulgus ritae
King, Sangster, Trainor, Irestedt, Prawiradilaga & Ericson, 2024
 
Timor Nightjar  |  Cabak Timor  ||  DOI: 10.1111/ibi.13340  
photo by James Eaton

Abstract
The nightjars of the Caprimulgus macrurus complex are distributed from Pakistan to Australia and comprise six morphologically similar but vocally distinct species. Fieldwork on Timor and Wetar, Lesser Sunda Islands, has resulted in the discovery of a seventh species in the complex, which we describe as a new species. This species has previously been confused with Caprimulgus macrurus, Caprimulgus celebensis and Caprimulgus manillensis but it differs from these and all other species in the complex by at least 13 vocal characters. Discriminant function analysis correctly classified all recordings in the complex to species. Caprimulgus ritae is known from five adult museum specimens, which are the smallest in the complex and which differ from other species in the complex in several morphological characters. A molecular phylogenetic analysis indicated that C. ritae is sister to C. meesi from Flores and Sumba, and that these species together are sister to C. macrurus. C. ritae is a tropical forest specialist occurring from sea level to at least 1500 m (probably mostly below 1000 m). Lowland and montane forests on Timor are threatened. Wetar is one of the least developed islands in Indonesia, and retains >95% natural vegetation, dominated by Eucalyptus woodlands, with tropical forests in river gorges and slopes in upland areas. Pressure for development is accelerating throughout the range of C. ritae, and a detailed assessment of its conservation status is urgently needed.
 
Male Caprimulgus ritae, Wetar, 13 October 2014 (James Eaton).
This bird was sound recorded (XC204788 and XC204789).

Caprimulgus ritae sp. nov.
Timor Nightjar | Cabak Timor

 
Ben F. King, George Sangster, Colin R. Trainor, Martin Irestedt, Dewi M. Prawiradilaga and Per G. P. Ericson. 2024. A New Species of Nightjar (Caprimulgus) from Timor and Wetar, Lesser Sunda Islands, Wallacea. Ibis. DOI: 10.1111/ibi.13340 
 

Thursday, November 17, 2022

[Entomology • 2022] Indigryllus sagani • A New Species of Indigryllus (Orthoptera: Gryllidae: Eneopterinae: Xenogryllini) from Kerala, India, with First Data on Acoustics and Natural Habitat


Indigryllus sagani
Jaiswara, Sreebin, Monaal & Robillard, 2022

 
Abstract
In India, the cricket subfamily Eneopterinae is represented by two known genera, Xenogryllus Bolívar, 1890 and Indigryllus Robillard & Jaiswara, 2019. The latter was recently described and is known from a single species I. kudremu Robillard & Jaiswara, 2019 from Karnataka, India. The species was known exclusively from its morphological features and there existed no information on its biology and acoustic features. The present study is a step ahead in understanding the natural history and acoustic signalling in the genus. Based on a collaboration initiated by citizen science observations on the website iNaturalist, we describe a new species, Indigryllus sagani sp. nov. from Kerala, India, with details on its habitat and acoustic signals.

Keywords: Orthoptera, calling song, Citizen science, courtship, taxonomy, Western Ghats 




 Indigryllus sagani sp. nov.

 
Ranjana Jaiswara, S. Sreebin, Monaal and Tony Robillard. 2022. A New Species of Indigryllus (Orthoptera, Gryllidae, Eneopterinae, Xenogryllini) from Kerala, India, with First Data on Acoustics and Natural Habitat. Zootaxa. 5205(6); 532-546. DOI: 10.11646/zootaxa.5205.6.2

Monday, January 25, 2021

[Entomology • 2021] Three New Species of the Genus Mata Distant, 1906 (Hemiptera: Cicadidae: Cicadinae: Oncotympanini) with Notes on Their Natural History from Meghalaya, India


Mata lenonia 
Sarkar, Mahapatra, Mohapatra, Nair & Kunte, 2021

 facebook.com: Vivek Sarkar 

Abstract
Three new species of the Asian genus Mata Distant, 1906 (Hemiptera: Cicadidae) viz. Mata lenonia sp.nov.; Mata ruffordii sp.nov. and Mata meghalayana sp.nov. are described from Indian state of Meghalaya. Keys and taxonomic descriptions of these species are provided with detailed accounts of their natural history and acoustics.

Keywords: Hemiptera, Indo-Burma Biodiversity Hotspot, Cicada, Mata, Species Discovery, Natural History, Meghalaya




Mata lenonia 



Vivek Sarkar, Cuckoo Mahapatra, Pratyush P. Mohapatra, Manoj V. Nair and Krushnamegh Kunte. 2021. Description of Three New Species of the Genus Mata Distant, 1906 (Hemiptera: Cicadidae: Cicadinae: Oncotympanini) with Notes on Their Natural History from Indian State of Meghalaya, India. Zootaxa. 4908(1); 1–28. DOI: 10.11646/zootaxa.4908.1.1

Wednesday, November 4, 2020

[Herpetology • 2020] Allobates velocicantus • A New Nurse Frog (Anura: Aromobatidae) from Brazilian Amazonia with A Remarkably Fast Multi-noted Advertisement Call


Allobates velocicantus 
Souza, Ferrão​, Hanken & Lima, 2020


Abstract 
Nurse frogs (Aromobatidae: Allobates) are probably the most extensively studied genus by taxonomists in Brazilian Amazonia. The southwestern portion of Amazonia is the most species-rich: as many as seven species may occur in sympatry at a single locality. In this study, we describe a new species of nurse frog from this region. The description integrates data from larval and adult morphology, advertisement calls and DNA sequences. Allobates velocicantus sp. nov. is distinguished from other Allobates mainly by the absence of hourglass-shaped dark marks on the dorsum and dark transverse bars on the thigh; a throat that is white centrally and yellow marginally; basal webbing on toes II and III; finger I longer than finger II; and an advertisement call composed of 66–138 pulsed notes with a note duration of 5–13 ms, inter-note intervals of 10–18 ms and a dominant frequency of 5,512–6,158 Hz. Tadpoles of the new species have 3–4 short, rounded papillae on the anterior labium, 16–23 papillae on the posterior labium, and a labial keratodont row formula 2(2)/3(1). This is the fifth species of Allobates described from the state of Acre, southwestern Brazilian Amazonia.

Figure 6: Coloration in life of adult Allobates velocicantus sp. nov.
 (A–C) Holotype, male, INPAH 41342, SVL = 15.3 mm. (D– F) Male, INPAH 41341, SVL = 15.4 mm. (G–I) Female, INPAH 41344, SVL = 16.6 mm. (J–L) Female, INPAH 41345, SVL = 17.4 mm. 
Photographs by Albertina Pimentel Lima.

Figure 10: Habitat and breeding behavior of Allobates velocicantus sp. nov.
 (B) A calling male (INPAH 41343). (C) A female ovipositing (uncollected). (D) Egg clutch containing 13 eggs with animal pole covered by melanin. (E and F) Male collecting tadpoles to transport to a pond (INPAH 41347). (G) Male with tadpoles on his back (INPAH 41347). In both clutches, eggs were deposited on the adaxial surfaces of green leaves.
 Photographs by Jesus R. D. Souza.


Allobates velocicantus sp. nov. 
Allobates sp. CdS MCP10187 (MCP10188) Grant et al. (2017).

Diagnosis. Allobates velocicantus sp. nov. is characterized by (1) small size, SVL 14.9–16.2 mm in males and 16.0–17.4 mm in females; (2) dorsal color pattern predominantly light brown, with no dark patches and marks; (3) dorsum granular; (4) dark brown lateral stripe from the tip of the snout to the groin; (5) light dorsolateral stripe absent or inconspicuous in living specimens but present in preserved specimens; (6) light but incomplete ventrolateral stripe; (7) oblique lateral line diffuse; (8) snout slightly rounded in dorsal view; (9) tympanum inconspicuous; (10) paired dorsal digital scutes; (11) supernumerary tubercles absent; (12) distal tubercle absent on finger IV; (13) discs moderately expanded on fingers I–IV; (14) finger I slightly larger than finger II; (15) finger III of males with similar width along phalanges; (16) dermal lateral fringes and webbing absent on fingers; (17) metacarpal ridge absent; (18) carpal pad absent; (19) excrescences on thumbs absent; (20) dark gland on arm absent; (21) basal webbing present between toes III and IV; (22) metatarsal tubercle present; (23) light “half-moon” shaped paracloacal mark; (24) superior eyelids dark brown; (25) iris metallic bronze; (26) pupil large, black, horizontal semielliptical; (27) transverse bars on thigh absent; (28) dark brown spots on tibia; and (29) advertisement calls formed by 66–138 pulsed notes (emitted in multiple exhalations) with a dominant frequency of 5,512–6,158 Hz.

Etymology. The specific epithet is derived from the Latin words velox (= fast) and cantus (= singing), in reference to the high note-repetition rate of the advertisement call of the new species. 
Proposed standard English name: fast singer frog. 
Proposed standard Spanish name: sapito del canto veloz. 
Proposed standard Portuguese name: sapinho do canto acelerado.

Phylogenetic placement. The new species is assigned to the genus Allobates based on its phylogenetic position presented in the present study and in Grant et al. (2017).


Figure 10: Habitat and breeding behavior of Allobates velocicantus sp. nov. 
(A) Understory of the lowland ombrophilous open forest at the type locality, municipality of Mâncio Lima, state of Acre, Brazil. (B) A calling male (INPAH 41343). (C) A female ovipositing (uncollected). (D) Egg clutch containing 13 eggs with animal pole covered by melanin. (E and F) Male collecting tadpoles to transport to a pond (INPAH 41347). (G) Male with tadpoles on his back (INPAH 41347). In both clutches, eggs were deposited on the adaxial surfaces of green leaves. 
Photographs by Jesus R. D. Souza.

Natural history notes. Allobates velocicantus sp. nov. inhabits the litterfall of primary and secondary lowland ombrophilous open forest (Fig. 10A). Populations of this species were found in terra firme forest either close to or distant from small forest streams. The new species uses leaves of small shrubs in the forest understory as egg deposition sites; two clutches (nine tadpoles and 13 eggs) were found in this situation. On 13–15 February 2019, during the middle of the rainy season, males were found calling between 8:00 and 18:00 h, and always perched between 10 and 30 cm above the ground. A pair of adults was observed courting: the male was leading the female to an egg deposition site, and he emitted a courtship call while both frogs were moving. As the male started emitting another advertisement call, the female stopped following. Arriving at the egg deposition site, the male jumped on to a leaf (adaxial surface), which was located around 20 cm above the ground, and continued to emit advertisement calls interspersed with courtship calls. After a few moments, the female jumped to the leaf with the male and approached him, initially touching snouts before turning her back to him. The male then jumped onto the female’s dorsum, while also sliding its hand to her head. The male remained in that position—cephalic amplexus—for 2 min before jumping from the leaf. The female remained in place for a few moments but then began moving, turning clockwise 30°, stopping, and repeating that pattern several times, always turning clockwise. The length of time the female stopped between movements ranged from 2 to 10 min, while she deposited eggs (Fig. 10C). Overall, egg deposition lasted 40 min before the female abandoned the leaf, leaving behind a clutch of 13 eggs. Each egg had a distinctly pigmented animal pole and was encased within cloudy jelly (Fig. 10D). The clutch was collected immediately after the female abandoned it, the embryos maintained alive through hatching, and the resulting tadpoles reared to Gosner stages 27–37 before being sacrificed and preserved.
 
The second egg clutch had nine tadpoles at aquatic-transport stage. The male (INPAH 41347) jumped onto the egg clutch and made circular movements inside it, at which time the tadpoles began to wriggle towards his dorsum, eventually climbing onto it (Figs. 10E–10G). This event lasted for 5 min.


Conclusion: 
Allobates velocicantus is differentiated from its congeners based on external morphology of adults and tadpoles, advertisement call and molecular analyses. The species represents an excellent model to study the ecological and physiological adaptations to solar radiation on eggs of Allobates. However, the conservation of A. velocicantus is threatened by the expansion of illegal logging, cattle ranching, and agriculture.


 Jesus R.D. Souza, Miquéias Ferrão​, James Hanken and Albertina P. Lima. 2020. A New Nurse Frog (Anura: Allobates) from Brazilian Amazonia with A Remarkably Fast Multi-noted Advertisement Call.  PeerJ. 8:e9979. DOI: 10.7717/peerj.9979

Friday, October 16, 2020

[Entomology • 2020] Cryptic New Species of Nesoecia Scudder, 1893 (Orthoptera: Tettigoniidae; Pseudophyllinae) from northeastern, Mexico


Nesoecia huichihuayan  
Barrientos-Lozano, Zaldívar-Riverón, Fernández-Azuara, Sánchez-Reyes & Almaguer-Sierra, 2020


Abstract
Nesoecia Scudder, 1893 is a neotropical genus of true katydids (Pseudophyllinae) comprising four species: N. brasiliensis (Bruner, 1915) from Brazil (Bahia), N. cooksonii (Butler, 1877) from Ecuador (Galápagos, Floreana Island), and two species from southern Mexico: N. insignis (Hebard, 1932) from Yucatán (Temax and Chichen-Itza), and N. nigrispina (Stål, 1873) reported also from Yucatán and the State of Tabasco (Teapa). Members of this genus are large and attractive insects, nonetheless, they have been poorly studied since they are not abundant or commonly collected. This paper describes four new species of Nesoecia from the Huasteca Region in northeastern México: N. huichihuayan n. sp., N. potoniya n. sp., N. insolita n. sp., and N. constricta n. sp. Taxa delimitation is based on morphological diagnostic characters and parameters of the acoustic signal. Information on distribution, habitat, and behavior is provided.

Keywords: Orthoptera, Pseudophyllinae, true katydids, morphology, acoustic signal, behavior



Ludivina Barrientos-Lozano, Aurora Y. Zaldívar-Riverón, Geovany J. Fernández-Azuara, Uriel Jeshua Sánchez-Reyes and Pedro Almaguer-Sierra. 2020. Cryptic New Species of Nesoecia Scudder, 1893 (Orthoptera: Tettigoniidae; Pseudophyllinae) from northeastern, Mexico. Zootaxa. 4859(4); 451–486. DOI: 10.11646/zootaxa.4859.4.1

Saturday, January 12, 2019

[Herpetology • 2019] Microhyla aurantiventris • A New Species of the Genus Microhyla Tschudi, 1838 (Anura: Microhylidae) from Tay Nguyen Plateau, Central Vietnam


Microhyla aurantiventris 
Nguyen, Poyarkov, Nguyen, Nguyen, Tran, Gorin, Murphy & Nguyen, 2019



Orange-bellied Narrow-mouth Frog  ||  DOI: 10.11646/zootaxa.4543.4.4  

Abstract
We describe a new species of Microhyla from Tram Lap forest, Gia Lai Province, Central Vietnam based on morphological, molecular, and acoustic data. The new species resembles M. butleri morphologically, but differs from all congeners by a combination of the following morphological attributes: (1) medium-sized adult snout–vent length 25.2–27.0 mm in 15 males and 30.5 mm in a single female; (2) body habitus moderately stocky; (3) head flat, snout rounded, slightly prominent in ventral profile; (4) dorsum and flanks slightly shagreened with evenly scattered tiny tubercles, ventral skin smooth; (5) first finger well developed, more than one-half the length of the second finger; (6) tips of three outer fingers slightly enlarged, forming weak disks and tips of all toes distinctly dilated into wide disks with narrow peripheral grooves; (7) finger and toe disks with dorsal median longitudinal grooves; (8) three palmar tubercles and two metatarsal tubercles; (9) tibiotarsal articulation of adpressed limb reaching slightly beyond the orbit; (10) webbing formula: I 1¾–2 II 1½–2¾ III 2–31/3 IV 3¼–1½ V; (11) in life, chin and throat yellowish to bright-orange with tiny dark brown speckling laterally; and (12) a call consisting of 15–26 pulses with a dominant frequency of 1.8–2.2 kHz (recorded at 18.5ºC). We also provide a preliminary genealogy of Microhyla based on analysis of a 2644 bp fragment of 12S–16S rRNA mitochondrial DNA. Based on the examed data, the new species and M. butleri are sister-species (genetic p-distance: 9.0%) and it can be distinguished from M. butleri by its morphology (size, webbing on toes, color) and advertisement call. Interspecific genetic p-distances between the new species and its congeners vary from 9.0% to 14.8%. Microhyla aurantiventris sp. nov. occurs in evergreen montane tropical forests at elevations around 1200 m a.s.l. and is known only from the type locality. The new species appears to be threatened due to intensive logging and agriculture plantation.

Keywords: Amphibia, Acoustics, amphibians, mtDNA genealogy, Microhyla aurantiventris sp. nov., Microhylinae, Tram Lap Forest, Gia Lai Province






FIGURE 1. Type locality (red dot) of Microhyla aurantiventris sp. nov. in Gia Lai Province, Vietnam.

FIGURE 5. Male holotype of Microhyla aurantiventris sp. nov. in life.
A, dorso-lateral view; B, dorsal view; C, ventral view; D, palmar view of left hand; E, thenar view of left foot; and F, iris coloration. (Note: the semicircle seen in the eye of frog in F is from a ring flash and not a natural coloration). Photos by L.T. Nguyen.

Microhyla aurantiventris sp. nov.

Etymology. The specific name “aurantiventris” is a Latin adjective in the nominative singular, feminine gender, derived from “aurantiacus”—“orange-colored” and “venter”—“belly”, referring to the distinctive bright orange-yellow coloration of ventral surfaces in adult males of the new species.
The recommended common name in English is “Orange-bellied narrow-mouth frog”.
The recommended common name in Vietnamese is “Nhái bầu bụng vàng”.

Distribution. Microhyla aurantiventris sp. nov. is currently known only from the type locality in ...., Gia Lai Province, Vietnam (Fig. 1). The species was recorded from elevation ca. 1210 m a.s.l. The distribution of the new species is unknown, and discovery of new localities within the Kon Tum Plateau is anticipated.





FIGURE 9. Breeding habitat of Microhyla aurantiventris sp. nov. at the type locality in Tram Lap forest, Gia Lai Province; note the dead trees due to construction of a new road across the forest.

FIGURE 10. The four sympatric species of Microhyla recorded at the type locality of Microhyla aurantiventris sp. nov. (Vietnam, Gia Lai Province, Tram Lap Forest).
A, M. butleri; B, M. heymonsi; C, M. mukhlesuri; and D, M. pulverata.


Luan Thanh Nguyen, Nikolay A. Jr. Poyarkov, Tiep Tan Nguyen, Tam Ai Nguyen, Vy Huu Tran, Vladislav A. Gorin, Robert W. Murphy and Sang Ngoc Nguyen. 2019.  A New Species of the Genus Microhyla Tschudi, 1838 (Amphibia: Anura: Microhylidae) from Tay Nguyen Plateau, Central Vietnam. Zootaxa. 4543(4); 549–580. DOI: 10.11646/zootaxa.4543.4.4  

    


Thursday, March 1, 2018

[Herpetology • 2018] Leptolalax rowleyae • A New Species of Leptolalax (Anura: Megophryidae) from Son Tra Peninsula, central Vietnam


Leptolalax rowleyae
Nguyen, Poyarkov, Le, Vo, Phan, Duong, Murphy & Nguyen, 2018

    DOI: 10.11646/zootaxa.4388.1.1 

Abstract

Morphological, acoustic and molecular analyses result in the description of Leptolalax rowleyae sp. nov., a new species of frog in the Megophryidae, belonging to the L. applebyi Rowley & Cao species group from central Vietnam. It differs from its congeners by a combination of the following morphological attributes: (1) adult SVL 23.4–25.4 mm in males and 27–27.8 mm in females; (2) presence of distinct dark/brown dorsolateral markings, including black spots on flanks; (3) pinkish milk-white to light brown chest and belly with numerous white speckles; (4) tympanum distinct; (5) absence of webbing or lateral dermal fringes on fingers and toes; (6) pectoral glands comparatively small (3.3–4.7% of SVL); (7) ventrolateral glands indistinct; and (8) iris bicolored with copper tint in upper half fading to golden in lower third of iris. The male advertisement call of the new species consists of 4–6 notes, lacking a distinct introductory note, with an average dominant frequency of 3.2–3.5 kHz. The description of the tadpole constitutes the first description of larval morphology for a member of the L. appleybi species group. Genetically, an uncorrected sequence divergence of 7.4% for 16S rRNA separates the new species from its two closest relatives, L. ardens and L. melicus in the L. applebyi species group.

Keywords: Amphibia, Acoustics, Leptolalax applebyi species group, tadpole morphology, Son Tra Nature Reserve








Luan Thanh Nguyen, Nikolay A. Jr. Poyarkov, Dzung Trung Le, Ba Dinh Vo, Hoa Thi Phan, Tang Van Duong, Robert W. Murphy and Sang Ngoc Nguyen. 2018. A New Species of Leptolalax (Anura: Megophryidae) from Son Tra Peninsula, central Vietnam.  Zootaxa. 4388(1); 1–21. DOI: 10.11646/zootaxa.4388.1.1


Friday, January 19, 2018

[Mammalogy • 2018] Uncovering the Diversity of Dog-faced Bats from the Genus Cynomops (Chiroptera: Molossidae), with the Redescription of C. milleri and the Description of Two New Species; Cynomops freemani & C. tonkigui


Cynomops freemani 
Moras, Gregorin, Sattler & Tavares, 2018


Abstract
Until recently the genus Cynomops (Chiroptera: Molossidae) comprised six species of fast flying, aerial insectivorous bats distributed throughout the Neotropics. However, our revisionary study have shown that the diversity of this taxon was underestimated as molecular and morphological data supported the recognition of C. milleri as a full species and revealed two previously unrecognized, small species of Cynomops. These newly recognized taxa are Cynomops freemani sp. nov. from the Canal Zone region, Panama, sister taxon to C. mexicanus, and Cynomops tonkigui sp. nov. from the eastern Andes of Ecuador and Colombia, sister taxon of C. milleri. We also describe the calls of Cynomops freemani sp. nov. that may be useful for the recognition of these species during field inventories based on ultrasonic recording techniques. We elevate the currently known diversity of Cynomops to eight species, as we also revalidate C. milleri providing an emended diagnosis and a redescription of this taxon.

Keywords: Free-tailed bats, taxonomy, acoustic identification, Cynomops freemani sp. nov, Cynomops tonkigui sp. nov

Systematics
Family Molossidae Gervais 1856
Genus Cynomops Thomas 1920

Cynomops milleri (Osgood, 1914)
Miller’s Dog-faced Bat




two Freeman’s Dog-Faced bats Cynomops freemani discovered in Gamboa, Panama.
Photo: Elias Bader

Cynomops freemani, new species 
Freeman’s Dog-faced Bat

ETYMOLOGY: The name “freemani” is in honor to Dr. Patricia W. Freeman in recognition of her influential contributions to the study of the morphology, systematics, and evolutionary relationships of molossid bats (e.g. Freeman, 1981).

DISTRIBUTION: Cynomops freemani is known from lowlands (23–53 m a.s.l.) of the Pacific coast of the Canal Zone region in Panama (Fig. 3).


 Waorani dog-faced bat Cynomops tonkigui 
Photo: Diego Tirira

Cynomops tonkigui, new species 
Waorani Dog-faced Bat

ETYMOLOGY: The name “tonkigui” is used as a noun in apposition, and means "bat" in the Waorani language. The name honors the Waorani people who inhabit the type locality (Tirira, 2012)

DISTRIBUTION: Cynomops tonkigui is known from the lowlands (195–529 m a.s.l.) of northeastern South America, and the eastern slopes of the Andes in Ecuador and Colombia (Fig. 3).


 Ligiane M. Moras, Renato Gregorin, Thomas Sattler and Valéria da C. Tavares. 2018. Uncovering the Diversity of Dog-faced Bats from the Genus Cynomops (Chiroptera: Molossidae), with the Redescription of C. milleri and the Description of Two New Species. Mammalian Biology. In Press. DOI: 10.1016/j.mambio.2017.12.005 

   

Two New Dog-Faced Bat Species Discovered in Panama and Ecuador newsdesk.si.edu/releases/two-new-dog-faced-bat-species-discovered-panama-and-ecuador
More sky puppies! Scientists discover two new species of dog-faced bat insider.si.edu/2018/01/sky-puppies-scientists-discover-two-new-species-dog-faced-bat 

Thursday, September 21, 2017

[Herpetology • 2017] Buergeria otai • Acoustic Differentiation and Behavioral Response reveals Cryptic Species within Buergeria Treefrogs (Anura, Rhacophoridae) from Taiwan


Buergeria otai 
Wang, Hsiao, Lee, Tseng, Lin, Komaki & Lin, 2017


Abstract

Buergeria japonica is a widely distributed treefrog occurring from Ryukyu Archipelago to Taiwan. Across this wide distributional range, we combined molecular, acoustic, morphological, and behavioral characters to clarify the taxonomic status among these insular populations. Genetic differentiation in mitochondrial sequences indicated an over 16% divergence among two deeply divergent clades: Japanese clade distributes in Ryukyu Archipelago and northwestern drainages of Taiwan, while Taiwanese clade distributes in the remaining drainages on Taiwan. The Taiwanese clade can be distinguished from the nominative species not only by molecular and morphological differences, but also distinguishable by considerable acoustic differentiation, which is extraordinarily noticeable for an additional type of long call that never recorded from Japanese clade. The two clades form a parapatric distribution pattern with narrow contact zones both in western and eastern Taiwan. Playback experiments indicated that male frogs show significantly stronger defensiveness against conspecific calls rather than heterospecific calls, indicating that these signals play a crucial role in species recognition. Here we describe the Taiwanese clade as a new species; the behavioral response and the magnitude of gene flow across their contact zones are especially worth for detailed studies.



Species description

Family Rhacophoridae Günther, 1859
Genus Buergeria Tschudi, 1838

Buergeria otai sp. nov.
Synonymy: 
Ixalus japonicus—Hallowell, 1861 "1860", Proc. Acad. Nat. Sci. Philadelphia, 12: 501. 
Polypedates japonicus—Stejneger, 1907, Bull. U.S. Natl. Mus., 58: 155. 
Rhacophorus (Rhacophorusjaponicus—Ahl, 1931 in Das Tierreich, 55: 111. 
Rhacophorus (Rhacophorusbuergeri japonicus—Wolf, 1936, Bull. Raffles Mus., 12: 166. 
Buergeria japonica—Liem, 1970, Fieldiana, Zool., 57: 90.

Etymology:  The specific epithet of the new species “otai” is a latinized patronymic noun in genitive case, dedicated to Prof. Hidetoshi Ota for his great contribution to herpetology and biogeography in East Asia, including Taiwan and adjacent regions. During 1980s to 1990s, Ota published four reptile species in Taiwan, carefully reviewed the herptile fauna across the East Asian Arc, and provided great assistance and encouragement to new-generation herpetologists in this region. We suggest the following common name “Ota’s stream tree frog” in English.

Diagnosis: Buergeria otai sp. nov. is characterized by a combination of the following characters: (1) a small-sized rhacophorid, body moderately slender; (2) SVL in adult males 23.1–29.3 mm (N = 133; mean ± SD = 26.57 ± 1.21 mm); females 29.7–37.5 mm (N = 3; 32.44 ± 4.42 mm); (3) dorsum slightly tubercular, with a pair of parallel tubercles on scapula; (4) head triangular, snout rounded and somewhat acute; (5) tips of fingers and toes dilated, forming expanded disks (over twice the width of phalanges); (6) tibiotarsal articulation on adpressed limb reaching beyond snout tip; (7) forelimb webbing absent; (8) hindlimb webbing partial, webbing formula (the number of phalanges free of web): I 1–1 II 1–2 III 1–1 IV 2–1 V; (9) vertebral stripe absent; (10) dark dorsal marking in the shape of inverted triangle between the eyes; (11) dark dorsal marking in a form of letter X or H extending from scapula to the middle of the back; (12) chin gray-white, with small irregular mottling; belly gray-white; (13) arms and thighs with sparse brownish bands; (14) regular tiny white spots on the ventral side of the thighs; usually concentrated at the base of the thighs.

Fig 6. Buergeria japonica (A, C) and Buergeria otai sp. nov. (B, D, E, F) in live. The irregular patches of B. japonica on the thighs could be compared to the regular tiny spots of Buergeria otai sp. nov., regardless the intraspecific variation from very few (E) to many (F).
Photographed by YJ Liang (A, C), CM Tsao (B), and HN Nguyen (D, E, F).

Natural history notes.
Although belonging to the Old-world treefrog family Rhacophoridae, Buergeria otai sp. nov. is specialized to live in the streams like all its congeners. They prefer to gather in small ditches or shallow waters near by the streams, but seldom entering into the major river course. Breeding season usually lasts from February to October, with a major peak from April to July (personal observation in this study), but may appear all year round in some habitats. Males gather to form chorus beside the streams after sunset, and the chorus reach its climax near midnight. Eggs 1.2–1.4 mm in diameter, attached on vegetation or spread on the substrates in shallow water, hatched after 24–36 hr. Tadpoles herbivorous or detritivorous, live benthically in shallow waters, with a larval stage period 15–30 days, depending on the water temperature.

Both Buergeria otai sp. nov. and B. japonica are well known for their special tolerance in geothermal hot springs, which seems to be an extraordinary adaptation from all anuran species in the world. The tadpoles of the frogs often show thermal affinity by approaching hot waters with temperature higher than 30°C, and their critical thermal maxima could reach more than 41°C. This adaptation was deduced to extend the breeding season, decrease the hatching rate, and increase the tadpole size. Furthermore, B. japonica was also well addressed for their special to salt tolerance. Although Buergeria otai sp. nov. is suspected to share the same tolerance, there was not yet an experiment designed to test this ability in this clade.


Ying-Han Wang, Yu-Wei Hsiao, Ko-Huan Lee, Hui-Yun Tseng, Yen-Po Lin, Shohei Komaki and Si-Min Lin. 2017. Acoustic Differentiation and Behavioral Response reveals Cryptic Species within Buergeria Treefrogs (Anura, Rhacophoridae) from Taiwan. PLoS ONE. 12(9); e0184005.  DOI:  10.1371/journal.pone.0184005



Tuesday, August 22, 2017

[Herpetology • 2017] Nasikabatrachus bhupathi • A New Species of the Genus Nasikabatrachus (Anura, Nasikabatrachidae) from the eastern Slopes of the Western Ghats, India


Nasikabatrachus bhupathi 
Janani, Vasudevan, Prendini, Dutta & Aggarwal, 2017 

We describe a new species of the endemic frog genus Nasikabatrachus, from the eastern slopes of the Western Ghats, in India. The new species is morphologically, acoustically and genetically distinct from N. sahyadrensis. Computed tomography scans of both species revealed diagnostic osteological differences, particularly in the vertebral column. Male advertisement call analysis also showed the two species to be distinct. A phenological difference in breeding season exists between the new species (which breeds during the northeast monsoon season; October to December), and its sister species (which breeds during the southwest monsoon; May to August). The new species shows 6 % genetic divergence (K2P) at mitochondrial 16S rRNA (1330 bp) partial gene from its congener, indicating clear differentiation within Nasikabatrachus. Speciation within this fossorial lineage is hypothesized to have been caused by phenological shift in breeding during different monsoon seasons—the northeast monsoon in the new species versus southwest monsoon in N. sahyadrensis. It is postulated that proximate triggers of breeding behavior and highly stenotopic adaptation of Nasikabatrachus tadpoles to inhabit cascades during monsoonal stream flows, have led to allopatry on the eastern and western slopes of the Western Ghats, thereby promoting speciation in this ancient genus.

Figure 3. Holotype of Nasikabatrachus bhupathi. (a) dorsolateral view; (b) anterior view of head showing fleshy protuberance on the snout; (c) underside of foot, showing hypertrophied shovel-shaped inner metatarsal tubercle; (d) underside of hand showing palmar tubercles.

Nasikabatrachus bhupathi sp. nov.

Etymology: The species epithet commemorates Dr. S. Bhupathy, a noted scientist and a field herpetologist, who passed away due to an ill-fated accident while conducting herpetological surveys in Agasthyamalai, Western Ghats on April 28, 2014.





Figure 10. External morphology of tadpoles of Nasikabatrachus bhupathi.
 (a) dorsal view; (b) ventral view at stage 36, with developing hind limbs, vent tube still present; (c) dorsal view at stage 41, with completely developed hind limbs and visible forelimb bud; (d) dorsal view at stage 42, with both forelimbs erupted; (e) ventral view at stage 42, where one of the forelimbs had erupted completely and the other is yet to erupt, absence of vent tube; (f) dorsal view at stage 43, with transforming snout; (gci) stage 44¢45, showing ventral and dorsal side, transforming oral disc and tail stub; (j) developed imago showing pigmentation pattern of brown and black mottles.


   

S. Jegath Janani, Karthikeyan Vasudevan, Elizabeth Prendini, Sushil Kumar Dutta and Ramesh K. Aggarwal. 2017. A New Species of the Genus Nasikabatrachus (Anura, Nasikabatrachidae) from the eastern Slopes of the Western Ghats, India. Alytes. 34: 1-19.