Showing posts with label Systematics. Show all posts
Showing posts with label Systematics. Show all posts

Tuesday, September 15, 2026

[Herpetology • 2026] Duttaphrynus phawngpui • A New Montane Toad Species (Anura: Bufonidae: Duttaphrynus) from Mizoram, northeastern India


Duttaphrynus phawngpui 
 Dawngliana, Warjri, Amarasinghe, Bal, Hruaia, Hlychho, Lalremsanga, Vabeiryureilai & Purkayastha, 2026


Abstract
We describe a new montane bufonid toad from Phawngpui National Park, Mizoram, northeastern India, using an integrative taxonomic approach combining morphology, multivariate morphometrics, and mitochondrial 16S rRNA sequence data. Phylogenetic analyses recover the Mizoram population as a well-supported lineage within the Duttaphrynus stuarti species group, distinct from its closest congeners, including D. stuarti, D. chandai, and D. dhara. Uncorrected 16S sequence divergence from currently recognised taxa ranges from 3.8–5.5%, consistent with species-level differentiation in Asian bufonids. Principal component analysis of size-corrected morphometric variables further supports its distinctiveness, with the new species occupying a discrete region of morphospace. The new species is characterized by moderate body size (SVL 47.72–56.26 mm), indistinct tympanum, absence of most cranial ridges, distinctive digital proportions, moderate toe webbing, and a dorsum with glandular warts, irregular dark blotches, and a narrow mid-dorsal stripe. Concordant molecular, morphometric, and morphological evidence supports its recognition as a distinct species. Known only from the type locality in high-elevation (>2000 m a.s.l.) montane habitats, the species highlights the importance of the Mizoram uplands for undocumented amphibian diversity within the Indo-Burma biodiversity hotspot.


Duttaphrynus phawngpui sp. nov 


Malsawm Dawngliana, Holiness Warjri, A. A. Thasun Amarasinghe, Amit K. Bal, Vanlal Hruaia, Mara D. Hlychho, Hmar T. Lalremsanga, Mathipi Vabeiryureilai and Jayaditya Purkayastha. 2026. A New Montane Toad Species (ANURA: BUFONIDAE: Duttaphrynus) from Mizoram, northeastern INDIA. TAPROBANICA. 15(2); 298–309. DOI: doi.org/10.47605/tapro.v15i2.423 [13 September 2026]  

Monday, September 14, 2026

[Botany • 2026] Begonia salog (Begoniaceae, sect. Baryandra) • A New endemic Species from southeastern Luzon, Philippines

 

Begonia salog Dela Cruz, Bucay, Corre, & Valiente, 

in Dela Cruz, Bucay, Corre, Valiente, Tandang et Chung, 2026. 
 
Abstract
Begonia salog, a member of section Baryandra, is characterized by rhizomatous growth, axillary protandrous inflorescences with boat-shaped bracts, and ovaries with bifid placentae. While sharing glandular hairs on the inflorescence with B. caramoanensis, it is distinguished by puberulent petioles (vs. tomentose), broadly serrated, non-ciliate leaf margins (vs. shallowly undulate and ciliate), a glabrous abaxial leaf surface (vs. pilose), glabrous bracts (vs. glandular-hairy), and a glabrous ovary (vs. glandular-hairy). Begonia salog is described here as a new species from the karst landscapes of southeastern Luzon, Philippines, with notes on its ecology and habitat, and a preliminary IUCN-based conservation assessment.

Keyword: Begonia caramoanensis, biodiversity conservation, comparative morphology, plant endemism, species delimitation


Begonia salog Dela Cruz, Bucay, Corre, & Valiente.
A. Habitat and habit; B. Rhizome, showing stipules and petiole base; C. Petiole showing vestiture; D. Adaxial leaf lamina; E. Abaxial leaf lamina; F. Staminate flower, face view; G. Pistillate flower, face view; H. Staminate flower, side view; I. Pistillate flower, side view; J. Inflorescence; K. Immature staminate flower showing the bracts and vestiture; L. Dissected stipule; M. Capsule; N. Ovary cross-section.
All from C.J.P. Dela Cruz 0016 (Holotype, PNH)

Begonia salog Dela Cruz, Bucay, Corre, & Valiente, sp nov.
 (§ Baryandra

Diagnosis: Begonia salog is characterized by its rhizomatous growth habit, axillary protandrous inflorescences with boat-shaped bracts, and an ovary exhibiting bifid placentation. Begonia salog is morphologically similar to B. caramoanensis (Rubite et al., 2020) in possessing glandular hairs on the inflorescences, but it can be distinguished by several key morphological traits. These include its puberulent (vs. tomentose) petioles; broadly serrate, non-ciliate leaf margins (vs. shallowly undulate to almost entire and ciliate); a glabrous abaxial lamina (vs. pilose with lightgreen to maroon hispid hairs denser along the veins) abaxial leaf lamina; glabrous (vs. glandular-hairy) bracts; and a glabrous (vs. glandular-hairy) ovary. Additional diagnostic differences between the two taxa are detailed in Table 1

Etymology: The epithet salog comes from the Bicolano word meaning ‘river,’ referring to the habitat where the plant was first documented.


Cyrus Job P. Dela Cruz, Mark Angelo C. Bucay, Karen B. Corre, Judy Ann V. Valiente, Danilo N. Tandang and Kuo-Fang Chung. 2026. Begonia salog (Begoniaceae, section Baryandra), A New endemic Species from southeastern Luzon, Philippines.  Taiwania. 71(4); 632-637 DOI: 10.6165/tai.2026.71.632 [10 August 2026] 

[Botany • 2026] Typhonium gonos • A New Species from Northern Thailand and a new synonym [Studies on Typhonium (Araceae: Areae) of Thailand VII]

 

 Typhonium gonos K.Z.Hein & Saensouk, 

in Hein, P. Saensouk, Rakarcha, Warseno et S. Saensouk, 2026.

Abstract
Typhonium gonos K.Z.Hein & Saensouk is described and illustrated as a species new to science, restricted to Permian limestone in Phrae Province, Northern Thailand, and compared with its probable closest congener, T. sinhabaedyae Hett. & A.Galloway from Tak Province. In addition, T. pusillum Sookch., V.D.Nguyen & Hett. is newly synonymized under T. gagnepainii J.Murata & Sookch.

Keyword: Aroideae, heterotypic synonym, Indochina, Northern Thailand, permian limestone, plant taxonomy

 Typhonium gonos sp. nov.
 A. Flowering individuals in habitat. B. Plants in habitat showing leaf blade variation within a population.
Photos by T. Uttarapong.

 Typhonium gonos sp. nov.
A. Excavated flowering plant. B. Leaf blade showing abaxial surface. C. Side view of anthomorph at pistillate anthesis. D. Front view of anthomorph at pistillate anthesis. E. Side view of anthomorph at pistillate anthesis (nearside spathe artificially removed to expose the spadix).
Scale bars: A–B.=3 cm, C–E.=5 mm. Photos by T. Sangchun and K.Z. Hein.

Detail of the spadices, each showing pistillate zone, sterile interstice, staminate zone and base of appendix (the near side of the spathe artificially removed).
A. Typhonium gonos sp. nov. B. T. sinhabaedyae.
Scale bars: A-B = 5 mm. Photos by T. Sangchun and K.Z. Hein.

Typhonium gonos K.Z.Hein & Saensouk, sp. nov. 

 Type: THAILAND. Northern: Phrae Province, Long District, Ta Pha Mok Subdistrict, elev. ca. 260 m, 11 May 2026, T. Uttarapong 001 (holotype: ! [spirit collection]; isotype: VMSU! [spirit collection]). 

Diagnosis: Typhonium gonos most closely resembles T. sinhabaedyae Hett. & A.Galloway (Fig. 3B) in its anthomorph, but differs in having a sterile interstice bearing distantly arranged staminodes only in the middle portion, with the lower and upper portions naked (vs. tightly arranged staminodes restricted to the lower part of the sterile interstice immediately above the pistillate zone in T. sinhabaedyae), and a stigma narrower than the ovary narrower than the ovary (vs. wider than the ovary in T. sinhabaedyae).

Etymology: The specific epithet gonos is derived from the Greek γόνος (gonos), meaning seed, semen, or seminal fluid, in allusion to the odour reminiscent of seminal fluid emitted by the anthomorph during pistillate anthesis, and is used as a noun in apposition. 

Details of the spadices of Typhonium gagnepainii showing variation in the shape of the staminodes (A.–C. All specimens originally collected from the same locality).
Scale bars: A-C = 5 mm. Photos by K.Z. Hein.


Khant Zaw Hein, Piyaporn Saensouk, Sarayut Rakarcha, Tri Warseno and Surapon Saensouk. 2026. Studies on Typhonium (Araceae — Areae) of Thailand VII: A New Species and a new synonym.  Taiwania. 71(4); 643-648. DOI: 10.6165/tai.2026.71.643 [12 August 2026]

[Herpetology • 2025] Liolaemus misti • A New Species of the Liolaemus walkeri clade (Squamata: Liolaemidae) in the volcanic chain of Arequipa, Peru


 Liolaemus misti 
Santa-Cruz, Canazas-Terán, Bejarano, López, Morales, von May, Catenazzi & Aguilar- Puntriano, 2025
   
 Salamandra. 61(2)

Abstract 
 We describe a new species of Liolaemus lizard from southwestern Peru, within the volcanic chain represented by the Chachani, Misti and Pichu Pichu volcanoes that surround the city of Arequipa. Te type locality is Simbral, in the district of Chiguata, Department of Arequipa. Te diagnostic characters of the new species include small size (SVL < 50 mm), a pigmented subocular scale, vertebral line generally absent or highly fragmented (when present), scales smooth or slightly keeled on the dorsal side of thighs, partial or total ventral melanism, and absence of precloacal pores in males and females. Te elevational distribution of the new species is 4135–5400 m a.s.l., with the upper limit representing the highest altitude record for a living squamate. 

Key words. Andes, high elevation, lizard, systematics, taxonomy.


Adult male holotype of Liolaemus misti sp. n. in life (MUSA 5708), SVL 49.1 mm, TL 55.0* mm.
(A) Dorsolateral, (B) ventral, (C) lateral head, (D) dorsal, and (E) absent precloacal pores. [* = Regenerated or broken tail.]

Adult female paratype of  Liolaemus misti sp. n. in life (MUSA 5709), SVL 45.5 mm, TL 45.2* mm.
(A) Dorsolateral, (B) ventral, (C) lateral head, (D) dorsal, and (E) absent precloacal pores. [* = Regenerated or broken tail.]



Liolaemus misti sp. n.  

Diagnosis: We assign Liolaemus misti sp. n. to the L. walkeri clade, lizards with throat or belly melanistic or with spots in males (Aguilar et al. 2013), small and slender (49.3 mm maximum SVL). Males of L. misti sp. n. differ from L. chavin and L. wari by their smaller size (less than 50 mm SVL vs 51.7–59.3 mm and 51.5–60.8 mm, respectively). Liolaemus misti sp. n. difers from L. tacnae by a lower number of midbody scales and dorsal scales (40–50 vs 48–59, 43–55 vs 53– 61, respectively). Te subocular scale and loreal scales are strongly pigmented in L. misti sp. n. whereas in L. walkeri these scales are lighter (Fig. 7). Te lateral felds in L. misti sp. n. have scattered black and white scales forming spots (males) or scattered black and brown scales (females), which are absent in L. pachacutec. Paravertebral marks appear as black complete marks or as fragmented lines (more noticeable when parallel to the dorsolateral stripe) in L. misti sp. n. (Figs 8A–9A), but they are absent or fuzzy in L. pachacutec; L. tacnae has paravertebral markings as black dots perpendicular to the dorsolateral stripe, with light scales behind the black scales (Figs 8C–9C). Te vertebral line is generally absent or highly fragmented in L. misti sp. n., but it is well diferentiated in L. chavin, L. pacachutec, L. walkeri, and L. wari. Liolaemus tacnae has keeled scales on the dorsal side of thighs, which are absent in L. misti sp. n. (Fig. 10). Liolaemus misti sp. n. also difers from L. pachacutec, L. walkeri, and L. wari in males lacking precloacal pores.

In Peru, three species of the L. alticolor-bribonii group have been confused with species of the L. walkeri clade: L. alticolor from Puno, L. chungara from Tacna, and L. incaicus from Cusco (Aguilar et al. 2013, Lobo et al. 2007, Quinteros et al. 2014, Valladares et al. 2021). Here we report key morphological diferences between these species and L. misti sp. n. Liolaemus misti sp. n. has 49–58 scales around the body, more than L. incaicus (34–46). Liolaemus misti sp. n. lacks keeled temporal scales which are present in L. chungara, L. incaicus (weakly keeled), and L. alticolor (markedly keeled). Dorsal scales in L. misti sp. n. are keeled and without a mucron, whereas a mucron is present in L. chungara. Liolaemus misti sp. n. has partial or total ventral melanism, which is absent in L. alticolor and L. incaicus. Liolaemus misti sp. n. lacks precloacal pores in males and females, which are present in some or all females of L. incaicus, and present in males of L. alticolor, L. chungara and L. incaicus.

Etymology: The scientifc epithet “misti” refers to the volcano Misti, in Quechua language means “a white man” referred to the snow or white blanket that covers the volcano, one of the greatest symbols and the most striking element of the landscape of the city of Arequipa. Misti is the most distinctive volcano of the three that surround the city, along with Chachani and Pichu Pichu. Arequipans say: “not in vain is one born at the foot of a volcano”, the presence of the Misti greatly infuences the noble spirit of its inhabitants.


Roy Santa-Cruz, Amaranta Canazas-Terán, Renato Bejarano, Evaristo López,Alberto Morales, Rudolf von May, Alessandro Catenazzi and César Aguilar-Puntriano. 2025. A New Species of the Liolaemus walkeri clade (Squamata: Liolaemidae) in the volcanic chain of Arequipa, Peru.  Salamandra. 61(2); 115-131.


[Mammalogy • 2026] Rhinolophus indorouxii • Resolving Taxonomic Ambiguity: A New cryptic Rufous Horseshoe Bat (Chiroptera: Rhinolophidae: Rhinolophus) from southern India

 
 Rhinolophus indorouxii  
Raman, Garg & Chattopadhyay, 2026
 

Abstract
Bats are the second largest group of mammals with high cryptic diversity. In this study, we describe the previously identified sibling species Rhinolophus indorouxii of the endemic rufous horseshoe bat Rhinolophus rouxii from Southern India. The species was discovered based on acoustic diversity and mitochondrial cytochrome b gene sequencing–based genetic distance metric and phylogenetic affinity. However, no detailed morphological description was available. We address this lacuna by presenting with a detailed morphological description along with acoustic and genetic (cytochrome oxidase I barcoding gene) data and identify species specific characters for future studies. This is an important step in recognizing the species diversity of Southern India, which is home to one of the global biodiversity hotspots.

Keywords: bat, taxonomy, systematics, Chiroptera, New species, Rhinolophidae, Western Ghats


 External appearance of Rhinolophus indorouxii sampled from Kerala part of southern Western Ghats. 
A—front view of the bat showing the noseleaf and ears, taken from Silent Valley National Park on 05 June 2018, B—dorsal view of the bat, taken Periyar Tiger Reserve on 12 July 2017,
C—lateral view of bat with brown coloration, taken from Kasargod Forest Division on 25 Nov 2018, D—bat having a combination of orange and brown coloration, taken from Ranipuram (Kasargod Forest Division) on 21 Feb 2018, E—bat with a combination of golden and orange coloration from Periyar Tiger Reserve on 12 July 2017, F—bat with dark-orange coloration from Periyar Tiger Reserve on 12 July 2017.
Images: Sreehari Raman. Not to scale.

The skull and mandible of Rhinolophus indorouxii, ♂ ZSI/WGRC/I.R.-V.4044 (holotype) from Dhoni reserve forest, Palakkad, Kerala, south India.
A—lateral views of the skull; B—lateral views of the mandible; C—dorsal view of the skull; D—occlusal view of skull; E—occlusal view of the mandible; F—frontal view of the mandible
Scale=10 mm.

 
Sreehari Raman, Kritika M. Garg and Balaji Chattopadhyay. 2026. Resolving Taxonomic Ambiguity: Description of A New cryptic Rufous Horseshoe Bat from Southern India Rhinolophus indorouxii sp. nov. Journal of Asia-Pacific Biodiversity. In Press, DOI: doi.org/10.1016/j.japb.2026.06.003 [24 July 2026]

Sunday, September 13, 2026

[Botany • 2026] Begonia trichopetiolata (Begoniaceae, sect. Baryandra) • A New Species from Bukidnon, Central Mindanao, the Philippines

 
Begonia trichopetiolata  Medecilo, Rubite & Caballes, 

in Medecilo-Guiang, Rubite, Vallejos, Atay et Caballes, 2026. 
Illustrated by Julieferd Torres facebook.com: Ferd Torres

Abstract
Begonia trichopetiolata from Bukidnon, Central Mindanao, is described and illustrated as a new species endemic to the Philippines. It closely resembles B. mabuhayensis from Surigao del Sur, Eastern Mindanao; however, it differs in having triangular, keeled stipules, densely villose petioles, leaves with 10 primary veins and non-repand margin, shorter inflorescences and primary peduncles, larger bracts, and smaller capsules. Following IUCN Red List criteria, we propose B. trichopetiolata as Critically Endangered (CR). This discovery raises the total number of Begonia species in Bukidnon to 14 and marks the third member of Begonia section Baryandra recorded in the province.

Eudicots, Critically endangered, karst forest, limestone, Mindanao, Philippine endemic

Begonia trichopetiolata.
A. Habit; B. Detail of petiole; C. Leaf abaxial surface; D. Staminate flower bud; E. Staminate flowerfront view; F. Staminate flower lateral view; G. Stamens; H. Anther and filament; I. Pistillate flower front view; J. Pistillate flower lateralview; K. Stigma and style; L. Lateral view of the stipule; M. Anterior view of the stipule; N. Cross section of the ovary; O. Capsule.
Illustrated by Julieferd Torres. 


Begonia trichopetiolata Medecilo, Rubite & Caballes sp. nov. 
§ Baryandra

Etymology:—The specific epithet trichopetiolata refers to the petioles entirely and densely covered with long white hairs.



Maria Melanie P. MEDECILO-GUIANG, Rosario R. RUBITE, Christian Jay S. VALLEJOS, Jasten Kerk A. ATAY and Ken Bien Mar L. CABALLES. 2026. Begonia trichopetiolata (section Baryandra, Begoniaceae), A New Species from Bukidnon, Central Mindanao, the Philippines.  Phytotaxa. 773(2); 162-170. DOI: doi.org/10.11646/phytotaxa.773.2.5 [2026-09-08]


Wednesday, September 9, 2026

[Herpetology • 2026] Dibamus alfredi & D. somsakiLong time no see: Rediscovery, first Molecular data, and Redescriptions of Two rare Dibamus Species (Squamata: Dibamidae) from Thailand

 

Dibamus somsaki Honda, Nabhitabhata, Ota & Hikida, 1997;
[A & B]  Dibamus alfredi Taylor, 1962

in KliukinPawangkhanant, Aksornneam, Kaosung, Nguyen, Bragin, Gorin, Suwannapoom, Thammachoti Charunrochana et Poyarkov, 2026. 

Abstract
Alfred’s blind skink, Dibamus alfredi Taylor, 1962, and Somsak’s blind skink, Dibamus somsaki Honda, Nabhitabhata, Ota & Hikida, 1997, are two poorly known and rarely recorded members of the family Dibamidae endemic to Thailand. Since their original descriptions based on specimens collected in Pattani Province in 1960 and Chanthaburi Province in 1995, respectively, both species have remained extremely elusive and no molecular data have been available to date. Here, we report new records of D. alfredi from Yala Province in southern Thailand and of D. somsaki from Chanthaburi Province in eastern Thailand, providing important new locality data for these rare Thai endemics. Based on newly collected material, we present revised diagnoses and detailed redescriptions of both species and provide osteological descriptions of D. alfredi and D. somsaki based on micro-CT data for the first time. In addition, we present the first molecular data for both species based on mitochondrial DNA sequences of three gene fragments (16S rRNA, ND2, and COI) and reconstruct an updated phylogeny of the family Dibamidae. Our analyses confirm that D. alfredi and D. somsaki represent two deeply divergent evolutionary lineages within the genus Dibamus.

Reptilia, Dibamus alfrediDibamus somsaki, blind skinks, rediscovery, molecular phylogeny, osteology, Indochina

Dibamus somsaki in life (ZMMU re-18399), female from Makham district, Chanthaburi, Thailand.
Photograph by P. Pawangkhanant.

Dibamus alfredi in life.
(A) female(B) male; from Yala, Thailand.
 Photographs by N.A. Poyarkov (A) and A. Kaosung (B).

Alfred’s blind skink, Dibamus alfredi Taylor, 1962
Somsak’s blind skink, Dibamus somsaki Honda, Nabhitabhata, Ota & Hikida, 1997



Nikita S. KLIUKIN, Parinya PAWANGKHANANT, Akrachai AKSORNNEAM, Andaman KAOSUNG, Tan Van NGUYEN, Andrey M. BRAGIN, Vladislav A. GORIN, Chatmongkon SUWANNAPOOM, Panupong THAMMACHOTI CHARUNROCHANA and Nikolay A. POYARKOV. 2026. Long time no see: Rediscovery, first Molecular data, and Redescriptions of Two rare Dibamus Species from Thailand (Squamata: Dibamidae).  Zootaxa. 5875(4); 301-332. DOI: doi.org/10.11646/zootaxa.5875.4.1 [2026-09-07]

Monday, September 7, 2026

[Ichthyology • 2026] Petulanos jasteri • A New Species of Petulanos (Characiformes: Anostomidae) from the Rio Araguari, Amapá State, Brazil

 

Petulanos jasteri
Birindelli, Lima & Gama, 2026


Abstract
The Neotropical family Anostomidae comprises over 150 valid species, though its true diversity remains underestimated. The genus Petulanos currently includes four species distributed across northern South America, all characterized by upturned mouths, compressed multicuspid dentition, and distinctive color patterns. In this study, we describe Petulanos jasteri, a new species apparently endemic to the rio Araguari, Amapá state, Brazil. Despite hosting extensive protected areas, Amapá remains poorly surveyed, and its ichthyofauna is still insufficiently documented. The new species is readily distinguished from congeners by its color pattern, consisting of three vertically elongated dark blotches on the posterior half of the trunk (without pale margins) combined with eight to ten dark vertical bars. It lacks the horizontal stripes that characterize P. brevior, as well as the rounded blotch above the pectoral fin present in P. intermedius, P. plicatus, and P. spiloclistron, and has 38 or 39 lateral-line scales (vs. 40 to 42 in P. spiloclistron). Osteological characters confirm its assignment to Petulanos, sharing synapomorphies such as four branchiostegal rays, bicuspid symphyseal premaxillary tooth, symplectic with a distinctive triangular ventral lamina, and open cranial fontanel. Petulanos jasteri, new species, is the first species of the genus reported from the rio Araguari. Its discovery emphasizes the underestimated diversity of the Anostomidae and highlights the need for further surveys and integrative studies in poorly explored basins of northern Brazil.

Petulanos jasteri.
(A) Holotype, IEPA 6078, 72.9 mm SL, Amapá, Ferreira Gomes, rio Mutum, tributary to rio Araguari, at Parque Nacional Montanhas do Tumucumaque.
(B) Paratype, ZUEC 14774, 83.7 mm SL, Amapá, Ferreira Gomes, rio Araguari.
(C) Paratype, ANSP 211099 (ex. IEPA 6079), 64.1 mm SL, rio Mutum, tributary to rio Araguari, at Parque Nacional Montanhas do Tumucumaque, photographed alive.
Scale bar = 10 mm. 

Petulanos jasteri, a new species 

Etymology.—The specific name jasteri honors Dr. Christoph Bernhard Jaster, formerly chief of the Tumucumaque National Park and the Amapá National Forest, for having made possible many field expeditions in these Conservation Units for the IEPA Ichthyology team, being a great supporter of basic science and biological surveys at Amapá State.


José L. O. Birindelli, Flávio C. T. Lima, Cecile S. Gama. 2026. New Species of Petulanos (Characiformes, Anostomidae) from the Rio Araguari, Amapá State, Brazil. Ichthyology & Herpetology. 114(3):451-460. DOI: doi.org/10.1643/i2025080 [28 August 2026]

Sunday, September 6, 2026

[Ornithology • 2026] Ducula tawitawi • A New Species of Imperial Pigeon (Aves: Columbidae: Ducula) from Tawi-Tawi, Philippines

 

Ducula tawitawi 
Halley, 2026

Tawi-Tawi Imperial Pigeon | DOI: doi.org/10.25226/bboc.v146i3.2026.a7

 Abstract 
Only three specimens of the Pink-bellied Imperial Pigeon Ducula poliocephala (G. R. Gray) are available from the isolated population on Tawi-Tawi Island, in the Sulu Archipelago, Philippines, and all have white (vs. brown) throats—a character shared with the closely related White-bellied Imperial Pigeon D. forsteni (Bonaparte). Two adults collected on Tawi-Tawi by the Menage Expedition, in 1891, are preserved in the National Museum of Natural History, Smithsonian Institution, Washington, DC. They bear archival labels with a nomen nudum (albigularis) indicating that the collectors initially considered them to be undescribed—because of the white throats—yet did not publish a description. A third white-throated specimen, collected in 1971 and preserved in the Delaware Museum of Nature & Science, Wilmington, confirms the morphological distinctiveness of the Tawi-Tawi population. Audio recordings from the 1990s further reveal that the Tawi-Tawi population is vocally distinct from D. poliocephala and D. forsteni. Based on its unique morphology and voice, I describe the ‘Tawi-Tawi Imperial Pigeon’ as a new species. It is endemic to the shrinking forests of Tawi-Tawi and faces an imminent risk of extinction.

Historic specimens of the ‘Tawi-Tawi Imperial Pigeon’Ducula tawitawi sp. nov. collected by Bourns and Worcester at Tataan (modern Tarawaken) during the Menage Expedition and held at the National Museum of Natural History, Smithsonian Institution, Washington, DC: (top left) USNM 314700, 21 October 1891; (bottom left) USNM 314701, 19 October 1891; the pale greenish-grey stains on the chins of these specimens were evidently caused by post-mortem fat migration (Matthew R. Halley; reproduced courtesy of the Bird Division, National Museum of Natural History, Smithsonian Institution, Washington, DC)

Ducula tawitawi sp. nov.
(left) Three views of DMNH 14999 and (right) its label and entry in the Delaware Museum of Nature & Science, Wilmington, ledger; the specimen was identified (apparently by duPont, see text) as ‘Ducula poliocephala nobilis’ when it was catalogued in 1972 (Matthew R. Halley)

Ducula tawitawi sp. nov.
Tawi-Tawi Imperial Pigeon

Diagnosis.—D. tawitawi has the pink belly of D. poliocephala (unlike D. forsteni) but the white throat of D. forsteni (unlike D. poliocephala). Its courtship or advertising song has a unique acoustic structure consisting of a low-amplitude buzz or ‘rattle’ followed by more notes (5–8) compressed into a shorter time interval, resulting in a higher tempo, than D. poliocephala and D. forsteni.

Geographic variation in throat colour in the Pink-bellied Imperial Pigeon Ducula [poliocephala] complex, as demonstrated by adult males held in the Delaware Museum of Nature & Science, Wilmington:
(A) DMNH 4501: Samar, May 1970; (B) DMNH 66314: Sibuyan, June 1973; (C) DMNH 1701: Mindanao, June 1961; (D) DMNH 14999: Tawi-Tawi, December 1971; (E) DMNH 10576: Mindoro, March 1971; (F) DMNH 66318: Marinduque, April 1972; (G) DMNH 3501: Luzon, March 1969 (Matthew R. Halley)


Matthew R. Halley. 2026. A New Species of Imperial Pigeon (Columbidae: Ducula) from Tawi-Tawi, Philippines. Bulletin of the British Ornithologists’ Club. 146(3); 295-310 DOI: doi.org/10.25226/bboc.v146i3.2026.a7 (2 September 2026)

Thursday, September 3, 2026

[Herpetology • 2026] Acanthosaura aurantiogularis • A New Species of the Genus Acanthosaura Gray, 1831 (Lacertilia: Agamidae) from the China-Myanmar Border Region in southwestern Yunnan Province, China


Acanthosaura aurantiogularis Wang, Lu & Che, 

in Wang, Lu, Zhao, Shi, Wan, Zhu, Jin et Che, 2026
橙喉棘蜥 | Orange-throated Pricklenape  ||  DOI: doi.org/10.3897/zookeys.1290.195408

Abstract
Using an integrative dataset of both mitochondrial DNA and morphological data, we describe a new species of the genus Acanthosaura from the China-Myanmar border region in Menglian County, Pu’er, Yunnan Province, China. The new species, Acanthosaura aurantiogularis sp. nov., is sister to A. tongbiguanensis, and it can be readily diagnosed from all recognized congeners by its bright orange gular coloration in the male, flesh colored oral cavity, moderate post-orbital spines and occipital spines, five or six well-developed nuchal crest scales, and a distinct dorsal coloration. We recommend further comprehensive phylogenetic studies of the genus and highlighted the understudied agamid diversity in northeastern Myanmar.

Key words: Agamid, Burma, cross-border, distribution, Draconinae, Pricklenape, taxonomy

Comparison between males (left column) and females (right column) of Acanthosaura aurantiogularis sp. nov. (top row, A, B) and closely related A. tongbiguanensis (bottom row, C, D) in life.
Photos by Zhuo-Yu Lu and Kai Wang.


Holotype male of Acanthosaura aurantiogularis sp. nov. (KIZ 61664) in life,
showing lateral overview (A), lateral closeup of body and head (B), ventral overview (C), and closeup of oral cavity (D).
Photos by Zhuo-Yu Lu.

Paratype female of Acanthosaura aurantiogularis sp. nov. (KIZ 61665) in life,
showing lateral overview (A), lateral closeup of body and head (B), ventral overview (C), and closeup of oral cavity (D).
Photos by Zhuo-Yu Lu.
 
Acanthosaura aurantiogularis Wang, Lu & Che, sp. nov.

Diagnosis. Acanthosaura aurantiogularis sp. nov. can be diagnosed from congeners by a combination of the following morphological characters: (1) tail short, TAL 167% SVL in female; (2) length of post-orbital and occipital spines moderate, LOPS 11.0–15.1% HL, LLOC 9.5–15.9% HL; (3) nuchal crest erected, 5 or 6, discontinuous from dorsal crests, TNCL 13.8–18.7% HL; (4) diastema short, composed of 6–8 small scales; (5) dorsal crest erected, anterior most one shorter than nuchal, decreasing in length posteriorly; (6) enlarged middorsal crest scales 41; (7) gular pouch moderately developed, transverse gular fold ...

Etymology. The specific epithet aurantiogularis is a compound Neo-Latin adjective derived from the Latin aurantius, meaning “orange-colored,” and gularis, meaning “the throat”. This nomenclature is a direct descriptor of the lizard’s most striking and diagnostic morphological feature: the vibrant, unmarked orange-yellow gular pouch in males. The suggested Chinese common name is “橙喉棘蜥” (Pinyin: Chéng Hóu Jí Xī), and the suggested English common name is Orange-throated Pricklenape.


 Kai WANG, Zhuo-Yu LU, Gui-Gang ZHAO, Wei SHI, Ru-Wen WAN, Na ZHU, Jie-Qiong JIN and Jing CHE. 2026. A New Species of the Genus Acanthosaura Gray, 1831 (Reptilia, Lacertilia, Agamidae) from the China-Myanmar Border Region in southwestern Yunnan Province, China. ZooKeys. 1290: 319-337.  DOI: doi.org/10.3897/zookeys.1290.195408 [27 Aug 2026]

Sunday, August 30, 2026

[Crustacea • 2026] Cambarus emegi • A New Stream-dwelling Species of Cambarus (Decapoda: Cambaridae) from Virginia and Pennsylvania (USA) with Notes on its Distribution, Ecology, and Conservation Status

 

Cambarus emegi 
Lieb, Williams, Foltz & Loughman, 2026 
 

Abstract
A new species of crayfish, Cambarus emegi sp. nov., is described from the upper James and Roanoke River basins in Virginia and the lower Delaware River basin in Pennsylvania, where it occurs in streams and small rivers. The species was formerly part of the Cambarus acuminatus species complex (Cambarus species C complex), a long-standing taxonomic enigma that is widely distributed across the Atlantic slope drainages of eastern North America. Cambarus emegi sp. nov. can be distinguished from Cambarus acuminatus due to the absence of a well-defined subpalmar tubercle, greater number of punctations across its areola, and differences in the mesial process of the form I male gonopod. Coloration and pattern in life differ between the two species. Additionally, the distributions of C. emegi sp. nov. and C. acuminatus are separated by hundreds of kilometers. The ranges of two other undescribed members of the Cambarus species C complex border that of C. emegi sp. nov. in Virginia. These species do not appear to overlap geographically; C. emegi sp. nov. is confined to the Ridge and Valley physiographic province, whereas the two undescribed species are found in the Blue Ridge and northern inner Piedmont regions. Cambarus emegi sp. nov. is morphologically similar but visually and genetically different from the undescribed species directly to the south in the upper Roanoke River system. Cambarus emegi sp. nov. is both visually and morphologically similar but genetically distinct from the undescribed species immediately downstream in the James River basin. Cambarus emegi sp. nov. is threatened by several potentially interacting factors including invasive crayfishes, narrow range, and urban and agricultural development. Alarmingly, the species is being rapidly replaced by invasive Faxonius species across a substantial part of its range. This paper represents an important step in providing the information needed to conserve and manage Cambarus emegi sp. nov.

Crustacea, Cambarus species C., Cambarus acuminatus, new species, Ridge and Valley, Northern Piedmont, Delaware, James, Roanoke, invasive crayfish

 Cambarus emegi sp. nov., color in life: (a) holotype, NCSM 95987; (b) allotype, NCSM 95988.

Life color and color pattern of adult  Cambarus emegi sp. nov.:
 (a) dorsal view; (b) oblique lateral view (photo credit Zackary A. Graham).

 Life color and color pattern of juvenile  Cambarus emegi sp. nov. 

Cambarus emegi sp. nov. 

Diagnosis.—Body and eyes pigmented. Rostrum weakly to moderately excavated and ventrally deflected anteriorly; rostral margins subparallel, pronounced and entire through acumen, and more thickened posteriorly than anteriorly; acumen acuminate with prominent dorsally deflected spiniform tubercle at terminus. Areola 2.2–3.6 (¯x=2.7, n=42, s=0.4) times as long as wide, with 6–10 (¯x=8.5, n=42, s= 0.7) punctations across narrowest point. Lateral portion of branchiostegal region of carapace heavily punctate; hepatic regions also punctate with welldeveloped tubercles. Strong cervical spines present; branchiostegal spine prominent; postorbital ridge terminating anteriorly in spiniform tubercle or spine. Weak to acute suborbital angle typically present, rarely absent; suborbital angle terminating anteriorly in spiniform tubercle or spine. Antennal basipodite spines prominent; ischiopodite spines present but not prominent.

Etymology.—Derived from the Turkish work “emeği” meaning “labor of” or “hard work of”, which seems appropriate given this project required many years and the collection of thousands of specimens from South Carolina to Pennsylvania. Additionally, the name honors Emily (Em) and Megan (Meg) Lieb, the senior author’s two daughters, who happily accompanied him on many crayfish sampling trips as children and later helped him collect C. emegi sp. nov. from sites in its Pennsylvania range. 

Common name.—We propose Enigma Crayfish as the common name.


David A. LIEB, Bronwyn W. WILLIAMS, David A. FOLTZ II and Zachary J. LOUGHMAN. 2026. Description of A New Stream-dwelling Species of Cambarus (Decapoda: Cambaridae) from Virginia and Pennsylvania (USA) with Notes on its Distribution, Ecology, and Conservation Status.  Zootaxa. 5857(2); 299-316. DOI: doi.org/10.11646/zootaxa.5857.2.5 [2026-07-29]