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[Paleontology • 2018] Qiupanykus zhangi • A New Alvarezsaurid Dinosaur from the Late Cretaceous Qiupa Formation of Luanchuan, Henan Province, central China

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Qiupanykus zhangi  
Lü, Xu, Chang, Jia, Zhang, Gao, Zhang, Zhang & Ding, 2018

 DOI:  10.31035/cg2018005 
Illustration: Zhao Chuang. 

An alvarezsaurid dinosaur skeleton was discovered from the Late Cretaceous Qiupa Formation of Luanchuan, Henan Province of centtral China. It represents a new alvarezsaurid dinosaur Qiupanykus zhangi gen. et sp. nov. A phylogenetic analysis recovers Qiupanykus nested within the unresolved clade, which includes Asian and north American taxa. The skeleton of the new specimen is preserved in association with eggshells. The eggshell morphologies show that these eggs belong to oviraptorid eggs, skeletal remains of which were discovered from the same area. The alvarezsaurid skeleton associated with eggshell fragments may indicate that these eggs were broken by the strong thumb-claws of the former and that alvarezsaurid dinosaurs may be egg-eaters.

Keywords: Vertebrate paleontology, alvarezsaurid dinosaur, Qiupanykus, Late Cretaceous, central China


Figure 2. The photograph (a) and outline drawings (b) of Qiupanykus zhangi.
 Abbreviations: cd: caudal vertebrae; f: femur; hc: haemal arch; il: ilium; mt(II-IV): metatarsls II-IV; ti: tibia; p: pubis; pp: pedal phalanx; sv: sacral vertebrae.

Systematic paleontology

Maniraptora (Gauthier, 1986)
Alvarezsauridae (Bonaparte JF, 1991)

Qiupanykus zhangi gen. et sp. nov.

Etymology: The generic name refers to the Qiupa town, Luanchuan County, where the specimen was discovered. The specific name is in honor of Shuancheng Zhang for his logistic support with fossil searching and excavations in the field.

Holotype: Incomplete skeleton comprising most posterior axial elements and most of hindlimb elements. The specimen 41HIII-0101 is housed in the collections of the Henan Geological Museum, Zhengzhou, China.

Holotype locality and horizon: The specimen (41HIII-0101) was found in Guanping, Qiupa Town, Luanchuan County of Henan Province; Qiupa Formation (Bureau of Geology and Mineral Resources of Henan Province, 1989; Lü JC et al., 2007)

Diagnosis: A small-sized alvarezsaurid dinosaur with the following combination of characters: posterior sacral vertebrae bearing a strong ventral keel; proximal caudals with transverse processes centrally positioned on centrum; pubic articular surface of the pubic peduncle of ilium is reduced and knob-like; fibular crest of tibia large and quadrangular; functional sacrum made up of eight vertebral elements (two anterior caudal plus six sacral vertebrae); a small pneumatic foramen is present in caudal vertebrae.
....

Figure 4. Life scene of Qiupanykus zhangi. 
(drawn by Zhao Chuang)

Behaviour of alvarezsaurid dinosaurs
The skeleton of Qiupanykus is associated with an eggshell fragment near its tail. The thickness of the eggshell fragment is 1.8 mm. Some features, such as linearituberculate ornamentation type, including nodes and short ridges, two structural layers (non-prismatic), and relatively thick shell, are all identical to the Luanchuan oviraptorosaur eggshells (Tanaka K et al., 2011). Using the formula (Elongatoolithidae) by Tanaka K et al. (2016), the estimated egg mass of the eggshell is: Log10 egg mass = 1.569×log10 (1.8)+2.655, the thickness of the egg shell is 1.8 mm, then the Egg mass is 1136.377 g (95% CI: 715 g to 1809 g). The femur circumference of Qiupanykus is 17.09 mm. Based on the formula (log10 BM = 2.754×log10(femur circumference-0.683) by Campione NE et al. (2014), the estimated body mass for Qiupanykus: is 515 g (log10 BM = 2.754×log10 17.09-0.683). The estimated egg mass is much heavier than the estimated body mass of Qiupanykus. Thus, the egg could not be laid by Qiupanykus.

Alvarezsaurid dinosaurs bear highly specialized arms, whose purpose is still a mystery. They are regarded that the special arms were used to burrow (Perle A et al., 1993) or break open termite mounds (like modern anteaters), and possible to feed on insects (Senter P, 2005). However, the skeleton is associated with eggshell fragments from Luanchuan area, and the eggshell fragment morphologies indicate that those eggs belong to oviraptorid eggs (Tanaka K, personal communication, 2017). There is another case found from north-western Patagonia of Argentina, where an alvarezsaurid skeleton is preserved with eggs (Agnolin FL et al., 2012). Although Agnolin et al. thought the eggs associated with the alvarezsaurid Bonapartenykus ultimus were laid by an alvarezsaurid dinosaur, they pointed out that the external ornamentation patterns of Arriagadoolithus expressed on the outer shell surface is similar to elongathoolithid eggs. Arriagadoolithus was possibly laid by oviraptorosaurid dinosaurs. Thus, there are three possibilities about the relationship between the alvarezsaurid skeletons and eggs (egg fragments) associated with them: (1) Eggshell fragments were buried with alvarezsaurid skeleton by coincidence, and the eggshell is nothing to do with the skeleton. (2) The eggs were laid by alvarezsaurid dinosaurs and (3) The eggshell fragments were from eggs broken by alvarezsaurid dinosaurs and the eggs were not laid by them. However, considering the strong thumb claw of alvarezsaurid dinosaurs, we prefer to the third interpretation. Alvarezsaurid dinosaurs perhaps use their special claw to break eggs, and they are perhaps egg-eaters (Fig. 4).


Conclusion: 
The skeleton of Qiupanykus is associated with oviraptorid egg shell fragments suggesting that at least the derived alvarezsaurid dinosaurs may be an egg-eaters, which use their special arms (the strong thumb claws) to pierce the hard eggshell. Qiupanykus is a relatively small sized alvarezsaurid and it represents the youngest alvarezsaurid dinosaur from China so far.




Jun-Chang Lü, Li Xu, Hua-Li Chang, Song-Hai Jia, Ji-Ming Zhang, Dian-Song Gao, Yi-Yang Zhang, Cheng-Jun Zhang and Fang Ding. 2018. A New Alvarezsaurid Dinosaur from the Late Cretaceous Qiupa Formation of Luanchuan, Henan Province, central China. China Geology. 1(1): 28–35. DOI:  10.31035/cg2018005

   


[Botany • 2018] Vepris bali (Rutaceae) • A New Critically Endangered (possibly Extinct) Cloud Forest Tree Species from Bali Ngemba, Cameroon

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Vepris bali Cheek

in Cheek, Gosline & Onana, 2018
  DOI:  10.3372/wi.48.48207 

Abstract 
Vepris bali is the first known species of Vepris in WC Africa with opposite, trifoliolate leaves and is further unusual for its long petiolules. Known only from Bali Ngemba Forest Reserve, a remnant of submontane forest under great pressure of degradation in the Bamenda Highlands of Cameroon, it may already be extinct due to tree cutting and agricultural incursions. Here, V. bali is compared with other endemic cloud forest Vepris of the Cameroon Highlands and is described, illustrated, mapped and assessed as Critically Endangered (Possibly Extinct) using IUCN 2012 criteria.


Fig. 1. Vepris bali. A: habit, flowering stem with male inflorescence; B: stem detail showing indumentum and lenticels; C: abaxial leaf surface showing oil glands; D: portion of partial-inflorescence showing bracts; E: male flower, side view; F: male flower, 2 sepals and petals removed and staminal filaments truncated; G: cross-section of rudimentary pistil.
 Drawn from the holotype, Ujor FHI 30422 (K), by Hazel Wilks.

Vepris bali Cheek, sp. nov. 
Toddaliopsisebolowensis sensu Letouzey (1963: 108), non Engl. (1917: 305).
Vepris cf. heterophylla sensu Mziray (1992: 73), non (Engl.) Letouzey (1966: 246).
– “Vepris sp. B” Cheek in Harvey & al. (2004: 55 [fig. 7], 124); Onana & Cheek (2011: 309).

Diagnosis — Differing from Vepris ebolowensis (Engl.) Onana in being a submontane tree, with a trunk c. 28 cm in diam, at 1.5 m from ground, leaves opposite, and median petiolules 9–14 mm long (whereas V.ebolowensis is a shrub of lowland forest, with leaves alternate, and median petiolules c. 0 mm long).

Holotype: Cameroon, Northwest Region, “Bamenda District, Bali-Ngemba Forest Reserve, in high forest on ... at the height of  1700 m. alt. with Uapaca sp., Garcinia sp., and Aningeria”, male fl., Mar 1951, Ujor FHI 30422 (K; isotype: FHI n.v.).
....

Etymology — The specific epithet is a noun in apposition, from the town and people of Bali in the Bamenda Highlands of the Northwest Region of Cameroon, near which, in the Bali Ngemba Forest Reserve, the only known locality for this tree is found.


Martin Cheek, George Gosline and Jean-Michel Onana. 2018. Vepris bali (Rutaceae), A New Critically Endangered (possibly Extinct) Cloud Forest Tree Species from Bali Ngemba, Cameroon. Willdenowia. 48(2); 285-292. DOI:  10.3372/wi.48.48207

New Tree Species Discovered — and Declared Extinct   therevelator.org/tree-discovered-extinct/

[Botany • 2018] Thismia kobensis (Thismiaceae) • A New and Presumably Extinct Species from Hyogo Prefecture, Japan

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 Thismia kobensis Suetsugu

in Suetsugu, Nakanishi, Kobayashi & Kurosaki, 2018

Thismia Griffith (1844: 221), Thismiaceae J. Agardh or Burmanniaceae sensu APG VI (2016), is one of the most species-rich mycoheterotrophic genera, consisting of ca. 80 species (Jonker 1948, Merckx et al. 2013). Considering that most of these species were collected only once (Jonker 1948) and that many new species have recently been discovered in various Asian countries (e.g. Suetsugu et al. 2017, 2018), many more undescribed species are likely in these regions.

Oxygyne Schlechter (1906: 140) is a rare, mycoheterotrophic plant genus that consists of six species. It has one of the most remarkable distributions of all angiosperm genera and is disjunct between Japan and western Central Africa (Cheek et al. 2018). Although O. hyodoi Abe & Akasawa (1989: 161) was described based on the specimens discovered in Ehime Prefecture, Kobayashi & Kurosaki (1993) noted that a specimen that was morphologically similar to O. hyodoi was also discovered in Kobe City, Hyogo Prefecture. However, the specimen differed from O. hyodoi in many features. As noted by Tsukaya (2016), characters such as the prominent annulus on the perianth tube suggested that it may not even belong to the genus Oxygyne. In addition, although it was identified as O. hyodoi based on its short perianth lobes (Kurosaki, personal communication), such flowers have also been noted in the genus Thismia (Tsukaya 2016). Therefore, it is highly probable that the specimen collected in Kobe was not O. hyodoi, but a Thismia species (Tsukaya 2016). 

So far, only one specimen of the putatively unknown Thismia species has been found, and two of the three inner perianth-lobes in this specimen were broken. In addition, the population was almost certainly destroyed during construction of an industrial complex, and no additional specimens have been found. Fortunately, the other parts of this specimen, including an inner perianth-lobe and all three of the outer perianth-lobes were completely preserved, so we conducted a taxonomic investigation using this specimen. Careful examination revealed that the unknown plant actually belongs to the genus Thismia. Here, we describe it as a new species, Thismia kobensis Suetsugu, as this specimen was found to have a significantly different floral morphology from the other known Thismia species. In addition, the unknown species belonged to the section Rodwaya Schlechter (1921: 38), as it had the vermiform, creeping roots, the inner perianth lobes without free filiform appendages and inner perianth lobes connivent at their apex. Here, we describe it as a new species, with discussions on the taxonomic validity of the section Glaziocharis (Taub. ex Warm.) Hatusima (1976: 4). 


FIGURE 2.  Thismia kobensis (from the holotype).
 A–B. Flowering plant. C. Flower, upper view. D. Flattened perianth tube. E. Stamens, inner view. F. Stamens, outer view. G. Style and stigma. Two broken inner perianth lobes are indicated by the dotted lines in A, B and D. 
Drawn by Kumi Hamasaki. Bar = 1 mm.

FIGURE 1.  Thismia kobensis (holotype) from the type locality.

Thismia kobensis Suetsugu, sp. nov. 
Type:— JAPAN, Hyogo Prefecture, Kobe City, Nishi-ku, Oshibedani-cho, Komi, ...alt. 200 m, 10 June 1992, Nakanishi & Kobayashi 22380 (holotype: HYO, in spirit collection).

Thismia kobensis is close to T. huangii Jiang & Hsieh (2011: 139) from Taiwan but differs in having a hexagonal prismatic perianth tube, white tepals and free stamens

 Distribution:— Japan (so far known from only type locality). 

Preliminary conservation status:— Extinct (EX). Thisima kobensis is known from only a single individual at Kobe City, Hyogo Prefecture. The specimen was collected in secondary forest dominated by Quercus serrata and Q. glauca in 10 June 1992. Although intensive surveys of the population discovered in June were conducted from 1992 to 1999, we did not discover additional T. kobensis plants. In 1999, the area was completely destroyed during the construction of an industrial complex. Since then, we have searched the surrounding intact areas in June each year but have failed to record any individuals. It is highly likely that the last individual has died, and this taxon is presumed extinct, although we need further efforts to discover additional individuals.

Notes:— According to Jonker (1938), Thismia kobensis belongs to the section Rodwaya, as it has vermiform and creeping roots, inner perianth lobes without free filiform appendages and inner perianth lobes that are connivent apically. In the section Rodwaya, T. kobensis is most similar to T.huangii from Taiwan, in having a dark-orange annulus, yellow and truncate connectives with hairs, stigma lobes with hairs and no nectaries. However, it is easily distinguished from T. huangii in having a hexagonal prismatic and less hairy perianth tube (vs. urn-shaped and densely hairy perianth tube), white tepals (vs. pale orange to yellow), and stamens free from each other (vs. adnate, forming a tube around the style). 

In addition, in having the stamens free from each other, T. kobensis is somewhat similar to T. abei (Akasawa) Hatusima (1976: 7) that belongs to the section Glaziocharis. So far, free stamens have not been reported in any species of Thismia except T. abei. However, T. kobensis clearly differs from T. abei in having a hexagonal prismatic perianth tube (vs. urn-shaped perianth tube), dark orange prominent annulus (white inconspicuous annulus), yellow rectangular connective (vs. white spatulate connective), outer perianth lobes without filiform appendages (vs. outer perianth lobes with long filiform appendages). Because appendages of the outer perianth lobes are considered a diagnostic character to distinguish sections Glaziocharis and Rodwaya (Kumar et al. 2017), we believe that T. kobensis is a member of Rodwaya. However, it should also be noted that several recent molecular studies suggested that the appendages of perianth lobes have little systematic significance in Thismia (Hunt et al. 2014, Merckx & Smets 2014, Kumar et al. 2017, Sochor et al. 2018). Actually, molecular results have clearly suggested that section Glaziocharis is not monophyletic and should be incorporated in section Rodwaya (Hunt et al. 2014, Merckx & Smets 2014, Kumar et al. 2017). Both our results (i.e., similarity of stamen morphology between T. kobensis and T. abei) and molecular analyses indicate that it is not necessary to distinguish Glaziocharis and Rodwaya as distict sections. 

Given that mycoheterotrophic plants are highly dependent on the activities of both the fungi and the trees that sustain them (Suetsugu et al. 2014, 2017b), they are particularly sensitive to environmental disturbance. Therefore, most mycoheterotrophic species are rare and seriously endangered. Furthermore, our study clearly indicated that some mycoheterotrophic plants have become extinct before being described. As the precise identification of most mycoheterotrophic plants requires detailed observations of floral organs that are hidden in the perianth tube (Tsukaya & Hidayat 2016, Suetsugu 2017a, b), re-examination of herbarium specimens will be useful for understanding both past and current diversity of the mycoheterotrophic flora. 


Kenji Suetsugu, Osamu Nakanishi, Tomiki Kobayashi and Nobuhira Kurosaki. 2018. Thismia kobensis (Burmanniaceae), A New and Presumably Extinct Species from Hyogo Prefecture, Japan.  Phytotaxa.  369(2); 121–125. DOI: 10.11646/phytotaxa.369.2.6

New plant species discovered in museum is probably extinct  kobe-u.ac.jp/research_at_kobe_en/NEWS/news/2018_09_13_01.html | Research at Kobe @KobeU_Global
New plant species discovered in museum is probably extinct  phys.org/news/2018-09-species-museum-extinct.html via @physorg_com


[Herpetology • 2018] Pristimantis tiktik • A New Minute Pristimantis (Anura: Strabomantidae) from the Andes of southern Ecuador

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Pristimantis tiktik 
 Székely, Eguiguren, Székely, Ordóñez-Delgado, Armijos-Ojeda, Riofrío-Guamán & Cogălniceanu, 2018

in Székely, Eguiguren, Székely, et al., 2018. 

Abstract
We describe a new rainfrog species (Pristimantis), from the wetland complex Oña, Nabón, Saraguro and Yacuambi, in the Andes of southern Ecuador, at altitudes ranging between 3000–3400 m a.s.l. Pristimantis tiktik sp. nov. is a small frog, displaying sexual dimorphism (the males with dorsum of various shades of gray, brown, orange or green and a whitish or pinkish yellow venter; females with brownish gray or gray dorsum and a reticulated white and black venter), with SVL ranging between 19.7–20.4 mm in females (n = 3) and 16.1–18.4 mm in males (n = 6). The skin on dorsum is tuberculated, that on venter is coarsely areolate, dorsolateral folds are absent, tympanic membrane is absent but the tympanic annulus is evident, cranial crests are absent, discs on fingers just slightly expanded, heel is lacking enlarged tubercles, inner edge of tarsus is bearing a long fold, Toe V is slightly longer than Toe III and the iris coloration is bronze with fine black reticulations. The males have a large subgular vocal sac that extends onto the chest and vocal slits but lack nuptial pads. The unique advertisement call consists of long duration series of periodically repeated clicks: “tik”. Molecular analyses place the new species in the recently resurrected P. orestes group, as the sister species of the assemblage that contains P. bambu, P. mazar, P. simonbolivari and an undescribed species.



Fig 2. Holotype of Pristimantis tiktik sp. nov. (MUTPL 239, adult male), SVL 16.7 mm, in life.
 A. Dorsolateral view; B. Ventral view; C. Dorsal view.

Class Amphibia Linnaeus, 1758
Order Anura Fischer von Waldheim, 1813

Superfamily Brachycephaloidea Günther, 1858
Family Strabomantidae Hedges, Duellman, and Heinicke, 2008
Subfamily Pristimantinae Pyron and Wiens, 2011

Genus Pristimantis Jiménez de la Espada, 1870

Pristimantis tiktik sp. nov. 
Székely, Eguiguren, Székely, Ordóñez-Delgado, Armijos-Ojeda, Riofrío-Guamán, and Cogălniceanu.

Fig 6. Color variation in males of Pristimantis tiktik sp. nov. in life.
 Paratype (MUTPL 240), SVL 18.4 mm: A. dorsolateral view; B. ventral view. Paratype (MUTPL 251), SVL 16.1 mm: C. dorsolateral view; D. ventral view. Paratype (MUTPL 277), SVL 17.0 mm: E. dorsolateral view; F. ventral view. 

Fig 7. Color variation in females of Pristimantis tiktik sp. nov. in life.
 Paratype (MUTPL 247), SVL 20.2 mm: A. dorsolateral view; B. ventral view. Paratype (MUTPL 252), SVL 19.7 mm: C. dorsolateral view; D. ventral view. Paratype (MUTPL 276), SVL 20.4 mm: E. dorsolateral view; F. ventral view.

Common English name. Tiktik Rain Frog
Common Spanish name. Cutín tiktik

Etymology. The specific name is the onomatopoeic representation of the frog’s particular call.

Holotype. MUTPL 239, an adult male (Figs 2, 3 and 5A) from Ecuador, Loja province, Saraguro canton, 21 km (by road) E of Urdaneta (3.58612° S, 79.07516° W; datum WGS84), 3300 m above sea level, collected by Paul Székely, Diego Armijos-Ojeda and Dan Cogălniceanu on 8 July 2016.
....

Diagnosis. We assign this species to Pristimantis based on phylogenetic evidence (Fig 1) and on the general morphological similarity to other members of the genus. Pristimantis tiktik is a small species distinguished by the following combination of traits: (1) skin on dorsum tuberculated; skin on venter coarsely areolate; discoidal fold weak, more evident posteriorly; thoracic fold absent; dorsolateral folds absent; low mid dorsal fold present; (2) tympanic membrane absent but tympanic annulus evident, its length about 30% of the length of eye; supratympanic fold present; (3) snout short, subacuminate in dorsal view, rounded in profile; canthus rostralis weakly concave in dorsal view, rounded in profile; (4) upper eyelid bearing several small tubercles, similar in size and shape with the ones from the dorsum, about 80% IOD in females and 70% IOD in males; cranial crests absent; (5) dentigerous processes of vomers inconspicuous, elongated, but each processes bearing 3 to 5 evident teeth; (6) males with a large subgular vocal sac, extended onto the chest; vocal slits present; nuptial pads absent; (7) Finger I shorter than Finger II; discs on fingers just slightly expanded, rounded; circumferential grooves present; (8) fingers bearing narrow lateral fringes; subarticular tubercles prominent; supernumerary palmar tubercles present, rounded, smaller than subarticular tubercles; palmar tubercle inconspicuous, bifurcated; thenar tubercle oval; (9) ulnar tubercles coalesced into low ulnar fold; (10) heel lacking enlarged tubercles; outer edge of tarsus with row of small tubercles; inner edge of tarsus bearing a long fold; (11) inner metatarsal tubercle broadly ovoid, about 3x round outer metatarsal tubercle; supernumerary plantar tubercles present; (12) toes bearing narrow lateral fringes; webbing absent; Toe V slightly longer than Toe III; discs on toes just slightly expanded, rounded, about same size as those on fingers; circumferential grooves present; (13) evident sexual dimorphism: in life, the males with dorsum of various shades of gray, brown, orange or green (brownish gray or gray in females), the flanks, chest, groins and ventral surface of the limbs have usually a reddish mottling and the venter is whitish or pinkish yellow (venter, axillae and groins white with black reticulum in females); iris bronze, with lower half darker, and with fine black reticulations; (14) SVL 19.7–20.4 mm in adult females (20.1 ± 0.36 SD, n = 3) and 16.1–18.4 mm in adult males (16.9 ± 0.79 SD, n = 6).


Fig 10. Habitat of Pristimantis tiktik sp. nov.  in the wetland complex of Oña, Nabón, Saraguro and Yacuambi.
A. One of the many glacial lakes from the wetland complex; B. General view of the herb páramo (montane grassland); C. Microhabitat with grasses and shrubs; D. Grass microhabitat near a stream from the wetland complex.

Distribution. Pristimantis tiktik is known only from the wetland complex of Oña, Nabón, Saraguro and Yacuambi (Fig 9) which spreads over three provinces, Loja, Azuay and Zamora-Chinchipe, in Southern Ecuador. This area has an altitudinal range between 3000 and 3400 m a.s.l. and consists of herb páramo (montane grasslands and shrublands) and a wetland complex of almost 100 glacial lakes (Fig 10). We found this species above 3000 m along the road that crosses this area from Urdaneta to Tutupali, but it is probably widespread in the entire wetland complex.


    

Fig 9. Distribution of Pristimantis tiktik sp. nov.  (red dots) in Ecuador. 

Natural history. All the specimens were encountered during the night on the grassy vegetation, very close to the ground (usually at 5–15 cm above the ground). The distinctive call of the males was heard throughout the year (usually after 18:00), regardless of the weather conditions, i.e. rain or strong winds. All the females were caught in the vicinity of the calling males. This seems to be one of the most common frog species from the wetland complex, along with Pristimantis aff. riveti. Other sympatric frog species include Gastrotheca pseustes and a currently undescribed species of Pristimantis.

Conservation status. Pristimantis tiktik is known only from the wetland complex of Oña, Nabón, Saraguro and Yacuambi, above 3000 m a.s.l., which is estimated to have an area of 192 km2. Even though this is one of the most commonly encountered species in the wetland complex, we consider it to be Endangered following B1ab(i,ii,iii)+2ab(i,ii,iii) IUCN criteria because: (1) its Extent of occurrence (EOO) and Area of occupancy (AOO) are estimated to be less than 200 km2; (2) it is known from only one location; and (3) its habitat is currently affected (or could be severely affected in the near future) by mining activities, invasive species (especially pines from the nearby pine plantations), grazing, wildfires and road constructions.


 Paul Székely, Juan Sebastián Eguiguren, Diana Székely , Leonardo Ordóñez-Delgado, Diego Armijos-Ojeda, María Lorena Riofrío-Guamán and Dan Cogălniceanu. 2018. A New Minute Pristimantis (Amphibia: Anura: Strabomantidae) from the Andes of southern Ecuador.   PLoS ONE. 13(8): e0202332.  DOI: 10.1371/journal.pone.0202332


[Ichthyology • 2018] Review of the Indo-West Pacific Genus Inimicus (Synanceiidae: Choridactylinae)

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Inimicus cuvieri (Gray, 1835)

in Inaba &  Motomura, 2018.

Abstract  
The stinger genus Inimicus Jordan & Starks, 1904 (family Synanceiidae), distributed in the Indo-West Pacific, is characterized by having two free pectoral-fin rays. Examination of the original descriptions and 420 specimens, including all available type specimens, of the genus resulted in the recognition of nine valid species: Inimicus brachyrhynchus (Bleeker, 1874) (recorded from Hong Kong and Singapore), I. caledonicus (Sauvage, 1878) (distributed in Andaman Sea and western Pacific Ocean), I. cuvieri (Gray, 1835) (Andaman Sea and western Pacific Ocean), I. didactylus (Pallas, 1769) (western Pacific), I. filamentosus (Cuvier, 1829) (western Indian Ocean), I. gruzovi Mandrytsa, 1991 (Coral Sea), I. japonicus (Cuvier, 1829) (East Asia), I. sinensis (Valenciennes, 1833) (eastern Indian and western Pacific oceans), and I. smirnovi Mandrytsa, 1990 (southwestern Pacific Ocean). Inimicusjoubini (Chevey, 1927), previously considered a valid species, is herein regarded as a junior synonym of I. japonicus. Another 10 nominal species are confirmed to be synonymized with the nine species. A revised diagnosis for each species and a key to all the species are provided.

Keywords: Pisces, stinger, taxonomy, synonym, morphology, distribution




 Tomoki Inaba and Hiroyuki Motomura. 2018. Review of the Indo-West Pacific Genus Inimicus (Synanceiidae: Choridactylinae). Zootaxa. 4482(1); 52–90.  DOI: 10.11646/zootaxa.4482.1.2

[Ichthyology • 2018] Monopterus rongsaw • A New Species of Hypogean Swamp Eel (Synbranchiformes: Synbranchidae) from the Khasi Hills in Northeast India

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Monopterus rongsaw
Britz, Sykes, Gower & Kamei, 2018


 A new species of hypogean swamp eel, Monopterus rongsaw, is described from the Khasi Hills in Meghalaya, India. It was discovered while digging rock-strewn and moist soil close to a small stream during attempts to find caecilians. The new species differs from other synbranchids by the combination of absence of skin pigmentation, the eyes being tiny and covered by skin, and a count of 92 precaudal and 69 caudal vertebrae.




Ralf Britz, Dan Sykes, David J. Gower and Rachunliu G. Kamei. 2018. Monopterus rongsaw, A New Species of Hypogean Swamp Eel from the Khasi Hills in Northeast India (Teleostei: Synbranchiformes: Synbranchidae). Ichthyological Exploration of Freshwaters. IEF-1086:1-12

New species of blind eel that burrows through the soil discovered

[Crustacea • 2018] Karstarma malang • A New Sesarmid Crab of the Genus Karstarma (Decapoda: Brachyura) Associated with Limestone Formations in East Java, Indonesia

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Karstarma malang
Wowor & Ng, 2018

  DOI:  10.11646/zootaxa.4482.2.7  

Abstract
A new stygobitic sesarmid crab species is described from underground freshwater cave streams in the southern Malang karst range on the south coast of East Java Province, Indonesia. Karstarma malang n. sp. is morphologically most similar to K. jacobsoni (Ihle, 1912) from an underground river cave system in the southern coast of the Special Region of Yogyakarta Province in central Java, but differs in having a relatively larger cornea, less swollen ocular peduncle which lacks a ridge along the median part, proportionately shorter ambulatory legs and a more slender male first gonopod. This paper increases the number of the species of Karstarma Davie & Ng, 2007, to 16; the new species being the eighth of the genus from Indonesia. It is also the third species which has a distinctly reduced cornea.

Keywords: Crustacea, Sesarmidae, Karstarma malang, new species, karst, caves, Java, Indonesia




Daisy Wowor and Peter K. L. Ng. 2018. A New Sesarmid Crab of the Genus Karstarma (Crustacea: Decapoda: Brachyura) Associated with Limestone Formations in East Java, Indonesia.  Zootaxa. 4482(2); 355–366.  DOI:  10.11646/zootaxa.4482.2.7

[Ichthyology • 2018] Speolabeo hokhanhi • A New Cavefish (Teleostei: Cyprinidae) from Central Vietnam

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Speolabeo hokhanhi
Tao, Cao, Deng & Zhang, 2018

Hokhanh’s Blind-cavefish  DOI: 10.11646/zootaxa.4476.1.10 

Abstract
Speolabeo hokhanhi, new species, is here described from Hang Va Cave in Phong Nha-Ke Bang National Park (Son River basin) in Central Vietnam. It can be distinguished from S. musaei by having no papillae on the lower lip, no hump immediately behind the head, a duckbilled snout, a shorter caudal peduncle (length 16.8–18.6% SL), and the pelvic fin inserted closer to the snout tip than to the caudal-fin base.

Keywords: Pisces, Speolabeo, new species, cavefish, Central Vietnam


FIGURE 2. Speolabeo hokhanhi sp. nov., fresh individual immediately after capture. Lateral view.

Speolabeo hokhanhi sp. nov.

Diagnosis. Speolabeo hokhanhi can be easily distinguished from S. musaei by having a lower lip without papillae (vs. with a band of papillae along its anterior margin), no hump immediately behind the head (vs. present), a duckbilled (vs. pyramidal) snout, the pelvic fin inserted closer to the snout tip than to the caudal-fin base (vs. midway between the snout tip and caudal-fin base) and a shorter (vs. longer) caudal peduncle (length 16.8–18.6% SL vs. 19.6–22.7). All data here used for S. musaei are from Kottelat and Steiner (2011).
....

Etymology. The specific epithet is named in honor of Mr. Ho Khanh who discovered many caves in Phong Nha–Ke Bang National Park. He was a local guide of the cavefish survey conducted by the first author during 2014 into the cave where the type specimens were collected and provided detailed information about the collection site.
 As common names, we suggest Hokhanh’s Blind-cavefish (English) 
and cá mù hang va hồ-khanh (Vietnamese).


 FIGURE 4. Distribution of Speolabeo hokhanhi (▲).

Distribution and habitat. Speolabeo hokhanhi is known only from the type locality (Fig. 4). Hang Va Cave is roughly 35 km south of Phong Nha village, rather close to Hang Son Doong, the world’s largest known cave that is 5 km long, 200 m high and 150 m wide. A 24 km southward drive along the West Ho–Chi–Minh highway starting from the tourism center of the Phong Nha–Ke Bang National Park leads to the point closest to the cave site of the Hang Son Doong. From there, roughly 1.5 hours’ northward walk following a narrow stony track through thick forest arrives at Hang Va Cave. Its entrance is about 30 meters above the ground. A descent of 15 m from the entrance reaches a cave passage containing a subterraneous stream. Downstream for approximately 200 meters, there is a shallow water pool with many stalagmites, usually 2–3 m tall (Fig. 5), where the type specimens of the new species were collected during the dry season. At this time, the pool had a muddy substrate and was 0.5–1.5 m in depth, 10 m wide, and 25 m long. More than 30 individuals of about the same size were observed in the pool; only six were captured using a hand-net. The fishes were swimming slowly and haphazardly, rather close to the water surface; when disturbed, they swam deeper, but did not seek shelter. A new shrimp species was found to sympatrically occur with the cavefish (Do & Nguyen 2014).


Nguyen Dinh Tao, Liang Cao, Shuqing Deng and E Zhang. 2018. Speolabeo hokhanhi, A New Cavefish from Central Vietnam (Teleostei: Cyprinidae). Zootaxa. 4476(1); 109–117.  DOI: 10.11646/zootaxa.4476.1.10
  


[Crustacea • 2018] Identity of the Tree-Spider Crab, Parasesarma leptosoma (Hilgendorf, 1869) (Decapoda: Brachyura: Sesarmidae), with Descriptions of Seven New Species from the Western Pacific

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Parasesarma macaco
 Li, Rahayu & Ng, 2018


Abstract
The identity of the tree-spider crab, Parasesarma leptosoma (Hilgendorf, 1869) (family Sesarmidae), which is believed to be widely distributed in the Indo-West Pacific, is reassessed and shown to be a species-complex with nine species, seven of which are here described as new. Parasesarma leptosoma sensu stricto is now restricted to South and East Africa; and P. limbense (Rathbun, 1914) from Sulawesi, which had been regarded as a junior synonym, is here recognized as a valid species. The following species are described as newP. gecko n. sp. from Vanuatu, Fiji, Guam and Japan; P. macaco n. sp. from Taiwan and the Philippines; P. kui n. sp. from Taiwan; P. parvulum n. sp. from the Philippines; P. gracilipes n. sp. from Indonesian Papua; P. purpureum n. sp. from Malaysia; and P. tarantula n. sp. from Sulawesi, Indonesia. The nine species of the Parasesarma leptosoma species-complex can be separated by the different shapes of their carapaces, the form of the dactylar tubercles on the male chelipeds, proportions of their ambulatory legs and the structure of the male first gonopod.

Keywords: Crustacea, Parasesarma, tree-climbing, species-complex, new species, taxonomy




 Jheng-Jhang Li, Dwi Listyo Rahayu and Peter K. L. Ng. 2018. Identity of the Tree-Spider Crab, Parasesarma leptosoma (Hilgendorf, 1869) (Decapoda: Brachyura: Sesarmidae), with Descriptions of Seven New Species from the Western Pacific. Zootaxa. 4482(3); 451–490. DOI:  10.11646/zootaxa.4482.3.2

[Herpetology • 2018] Systematic Revision of Calotes Cuvier, 1817 (Squamata: Agamidae) from the Western Ghats adds Two Genera and Reveals Two New Species

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Monilesaurus acanthocephalus  M. montanus
 Pal,Vijayakumar, Shanker, Jayarajan & Deepak, 2018


Abstract  
Lizards of the genus Calotes are geographically restricted to South Asia, Indo-China and parts of Southeast Asia. The greatest diversity of the genus is from the biodiversity hotspots in South Asia: Western Ghats (Peninsular India), Sri Lanka and Indo-Burma. Here, we present a systematic revision of members of the genus Calotes from Peninsular India using a combination of molecular phylogeny, geographical distribution and morphological characters. We show that Calotes from the Western Ghats is paraphyletic and consists of three major clades, one of which is widely distributed in South and Southeast (SE) Asia, while the others are restricted to Peninsular India. The Peninsular Indian clade is composed of two sister clades: Psammophilus, with a wider distribution and a second clade, composed of two extant species, Calotes rouxii and Calotes ellioti and two new species, all restricted to the Western Ghats region. Based on morphological differences, we retain the generic status of Psammophilus and assign its sister clade to a new genus Monilesaurus gen. nov. and transfer the following species, C. rouxii and C. ellioti, to this new genus. We also provide diagnoses and descriptions for two new species recognized within Monilesaurus gen. nov. In addition, Calotes aurantolabium from the Western Ghats was observed to be deeply divergent and to share a sister-relationship with the clade composed of CalotesMonilesaurus gen. nov., and Psammophilus. Based on its phylogenetic position and morphological attributes, we assign this species to a new genus Microauris gen. nov. These new discoveries highlight the evolutionary significance of the Western Ghats in housing novel lizard diversity.

Keywords: Reptilia, Agamidae, Calotes, new genus, MicroaurisMonilesaurusPsammophilus, Western Ghats


FIGURE 7. Lateral photograph showing live coloration of
 A. adult male Monilesaurus acanthocephalus gen. et sp. nov. and B. adult male Monilesaurus montanussp. nov. 

FIGURE 8. Lateral photograph showing live coloration of  adult female Microauris aurantolabium comb. nov.


Saunak Pal,S.P. Vijayakumar,Kartik Shanker ,Aditi Jayarajan and V. Deepak. 2018. A Systematic Revision of Calotes Cuvier, 1817 (Squamata: Agamidae) from the Western Ghats adds Two Genera and Reveals Two New Species. Zootaxa. 4482(3); 401–450. DOI: 10.11646/zootaxa.4482.3.1


[Botany • 2018] Miliusa chantaburiana (Annonaceae) • A New Species from southeastern Thailand

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Miliusa chantaburiana Damthongdee & Chaowasku

in Damthongdee & Chaowasku, 2018.

Abstract 
Miliusa chantaburiana Damthongdee & Chaowasku, a new species of Annonaceae from SE Thailand, is described and illustrated. It belongs to a clade with campanulate flowers and inner petals that are generally tightly appressed from the base to more or less the midpoint at anthesis. The new species is remarkable in possessing a strongly recurved apex of the inner petals at anthesis and can be principally differentiated from its morphologically closest species, M. pumila Chaowasku and M. filipes Ridl., both from Peninsular Thailand, by the higher number of stamens and carpels per flower and horseshoe-shaped stigmas. Miliusa chantaburiana is also unique in having a 6-base-pair insertion in the plastid matK sequence. A revised key to species in the campanulate-flowered clade in Thailand is given.

Keywords: Annonaceae, Chantaburi, matK, Miliusa, Miliuseae, new species, systematics, taxonomy, Thailand


Fig. 2. Leaf and flower of Miliusa chantaburiana 
A: abaxial (lower) leaf surface; B: adaxial (upper) leaf surface; C: flower, apical view showing stamens, carpels, inner petal discolouration and translucent window-like structures; D: flower, oblique view showing strongly recurved apical part of inner petals.

 – Scale bars: A = 2 cm; B = 10 cm; E = 1 mm; F = 0.5 mm. 
– A, B from cultivated material; C–F from Nakorn-Thiemchan NTC 29 (CMUB – spirit material).



Miliusa chantaburiana Damthongdee & Chaowasku, sp. nov.  

Holotype: Thailand, cultivated in Bangkok [sapling originally from Khiri Than Dam, Chantaburi Province], 7 Feb 2015 [in flower], Nakorn-Thiemchan NTC 29 (CMUB!; isotypes: B!, P!).

Diagnosis — Miliusa chantaburiana is morphologically close to M. pumila and M. filipes, both occurring in Peninsular Thailand (Chaowasku 2014). The new species differs mainly from M. pumila by having generally larger leaf blades ([9.2–] 12.2–18[–19.5] x [2.8–]3.3–6 cm vs 5.4–10.5 x 2–4.1 cm), generally longer pedicels ([11–] 14–22[–30] mm vs 5–11 mm), more stamens per flower (48–50 vs 38–39), and many more carpels per flower (49–71 vs 12–13). The new species primarily differs from M. filipes by possessing considerably more stamens (48–50 vs c. 22) and carpels (49–71 vs c. 16) per flower. In addition, M. chantaburiana exhibits horseshoe-shaped stigmas, whereas they are subglobose to ellipsoid(-obovoid) in M. pumila (Chaowasku 2014) and capitate in M. filipes.
....

Fig. 1. Holotype of Miliusa chantaburiana Damthongdee & Chaowasku, Nakorn-Thiemchan NTC 29 (CMUB).

Fig. 2. Leaf and flower of Miliusa chantaburiana – 
A: abaxial (lower) leaf surface; B: adaxial (upper) leaf surface; C: flower, apical view showing stamens, carpels, inner petal discolouration and translucent window-like structures; D: flower, oblique view showing strongly recurved apical part of inner petals; E: stamens attached to torus; F: carpel.
 – Scale bars: A = 2 cm; B = 10 cm; E = 1 mm; F = 0.5 mm. 
– A, B from cultivated material; C–F from Nakorn-Thiemchan NTC 29 (CMUB – spirit material).


Fig. 3. Flower, fruit and seed of Miliusa chantaburiana 
A: abaxial surface (outside) of an inner petal; B: adaxial surface (inside) of an inner petal; C: flower, basal view showing sepals and outer petals; D: fruit with five monocarps; E: flower with one inner petal pulled apart from others showing a mass of stamens and carpels; F: seed.
 – Scale bars: A, B, E, F = 5 mm; C = 3 mm; D = 2 cm.
 – A, B, E from Chaowasku 170 (CMUB – spirit material); C from Nakorn-Thiemchan NTC 29 (CMUB – spirit material); D from Chaowasku 171 (CMUB – spirit material); F from Nakorn-Thiemchan NTC 28 (CMUB – spirit material).

Distribution and ecology (at original locality) — Chantaburi Province, SE Thailand (Fig. 4); occurring in partially disturbed evergreen forests around a constructed dam; at an elevation of c. 205 m.

Conservation status — This species is known only from a very restricted area, i.e. around Khiri Than Dam of Chantaburi Province, SE Thailand (Fig. 4). Fewer than 10 individuals were observed in the area, some of which occur adjacent to the reservoir and could be submerged in the near future, and it is believed that many more individuals have been submerged during dam construction. Further, this species has never been reported to occur in nearby areas (e.g. Khao Khitchakut National Park, Khao Soidao Wildlife Sanctuary, Namtok Phliu National Park and Namtok Khlongkaew National Park) and no specimens have been collected prior to the present study. Based on this information, Miliusa chantaburiana is undoubtedly a rare species; however, we believe that more exploratory data, especially from Cambodia (which is merely c. 20 km away from the dam), are required prior to the assessment of the conservation status of this species. Therefore, it is considered here as Data Deficient (DD) (IUCN 2012).

Etymology — The epithet refers to Chantaburi, the SE Thai province where this species is endemic.


Anissara Damthongdee and Tanawat Chaowasku. 2018. Miliusa chantaburiana (Annonaceae), A New Species from SE Thailand. Willdenowia. 48(2); 293-301. DOI:  10.3372/wi.48.48208

    


    


[Herpetology • 2018] A Phylogenetic Ttaxonomy of the Cyrtodactylus peguensis Group (Squamata: Gekkonidae) with Descriptions of Two New Species from Myanmar; Cyrtodactylus meersi & C. myintkyawthurai

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Cyrtodactylus meersi  &  C. myintkyawthurai
Grismer​, Wood, Quah, Murdoch, Grismer, Herr, Espinoza, Brown & Lin, 2018


Abstract
A phylogenetic taxonomy of species in the Cyrtodactylus peguensis group from the Ayeyarwady Basin of Myanmar is constructed based on color pattern, morphology, and molecular systematic analyses using the mitochondrial gene NADH dehydrogenase subunit 2. Newly collected samples from the type locality of C. peguensis and other localities indicate that this clade is endemic to central Myanmar and contains at least seven species, four of which are undescribed. Three species, including C. peguensis occur in the low hills of the Bago Yoma Range within the central portion of the Ayeyarwady Basin. Two of these, Cyrtodactylus myintkyawthurai sp. nov. from the northern and central Bago Yoma and Cmeersi sp. nov. which is syntopic with Cpeguensis in the southern Bago Yoma are described herein. As more lowland hilly areas bordering, and within the Ayeyarwady Basin are surveyed, more new species of this group are likely to be discovered. These discoveries continue the recent surge of descriptions of new species of Cyrtodactylus that are being discovered in Myanmar.

....

Figure 1: Distribution map of the Cyrtodactylus peguensis group. Distribution of the species of the Cyrtodactylus peguensis group in the Ayeyarwady Basin and the adjacent foothills of the Chin Hills and Shan Hills in Myanmar.


Figure 5: Type specimens and additional specimen of Cyrtodactylus peguensis.
(A) Boulenger’s (1893) illustration of the lost syntype from the type locality of Hpa Lon, Bago Region Myanmar. (B) Syntype BM 946.8.23.10 from the type locality. (C) LSUHC 13454 from the Myin Mo Shwe Taung Pagoda, 9.5 km east of Hpa Lon, Bago Region Myanmar.
Photos by L. Lee Grismer.

Cyrtodactylus peguensis (Boulenger, 1893)
Pegu Bent-toed Gecko
Gymnodactylus peguensis Smith, 1921:29; 1935:52 in part. Wermuth, 1965:63 in part.
Cyrtodactyuls peguensis Taylor, 1963:728 in part; Denzer & Manthey, 1991:314 in part; Cox, Van Dijk & Nabhitabhata, 1998:87 in part; Pianka & Vitt, 2003:175 in part; Manthey & Grossmann, 1997:225 in part; Das, 2010:213 in part; Grismer et al., 2017a:91 in part; Brennan et al., 2017:3, in part.
Cyrtodactylus (Cyrtodactylyspeguensis Rösler, 2000:66 in part.

Syntype. Adult male BM 1946.8.23.10 collected in 1887 by Signor L. Fea from “Palon” (Hpa Lon), “Pegu” (Bago Region), Taikkyi Township, Yangon (north) District, Myanmar. Hpa-Lon is a small village in the Ayeyarwady Basin 9.5 km west of the western foothills of the southern portion of the Bago Yoma Range where Fea reported making zoological collections (Fea, 1897). Being that foothills are the closest suitable habitat for C. peguensis east of Pa-Lon, we restrict the type locality to the Myin Mo Swhe Taung Pagoda, Bago Region, Taikkyi Township, Yangon (north) District, Myanmar (..., elevation 162 m) situated within these foothills where we collected an additional specimen (LSUHC 13454). The other syntype could not be located.

Diagnosis. Cyrtodactylus peguensis differs from other species of the peguensis group by having the unique combination of seven supralabial and infralabial scales; 31 or 32 paravertebral tubercles; 17–19 longitudinal rows of dorsal tubercles; 36 or 37 ventral scales; 19 subdigital lamellae on the fourth toe; 17–19 femoral pores in males; eight precloacal pores in males; three rows of post-precloacal scales; and domed to weakly conical and weakly keeled body tubercles; and a maximum SVL of 70 mm (Table 7).


Figure 7: Holotype of Cyrtodactylus meersi sp. nov. (LSUHC 13455) from the type locality of the Myin Mo Shwe Taung Pagoda, Bago Division, Myanmar.
Photo by L. Lee Grismer.

Cyrtodactylus meersi sp. nov.
Bago Yoma Bent-toed Gecko

Diagnosis. Cyrtodactylus meersi sp. nov. differs from other species of the peguensis group by having the unique combination of seven supralabials and eight infralabials; 32 paravertebral tubercles; 13 longitudinal rows of body tubercles; 32 ventral scales; 17 subdigital lamellae on the fourth toe; 12 femoral pores; eight precloacal pores; two rows of post-precloacal scales; and domed to weakly conical and weakly keeled body tubercles (Table 7). We note, however, that this diagnosis is not robust due to having only a sample size of one juvenile and will be subject to adjustment if additional specimens are ever collected and analyzed. Nonetheless, the placement of this individual near the base of the phylogeny (Fig. 2) and it having an uncorrected percent sequence divergence of 10.0–13.7% from all other species in the phylogeny (Table 3) is strong evidence of its species status.

Distribution. Cyrtodactylus meersi sp. nov. is known only from the type locality of Myin Mo Shwe Taung Pagoda, 9.5 km east of the village of Hpa Lon, Bago Region, Taikkyi Township, Yangon (north) District Myanmar (Fig. 1).

Etymology. The specific epithet, meersi, is named in honor of Mr. John Meers whose generous private donations to Fauna & Flora International’s in the name of karst conservation have resulted in the continuation of karst biology research in Indochina.

Natural History. The holotype was collected in a region composed of low foothills and highly disturbed forest (Fig. 6). The specimen was encountered at 2,000 h as it was sitting in the middle of an ant trail, presumably preying on the ants. The fact that the specimen is a juvenile suggests the reproductive season is prior to May.



Cyrtodactylus myintkyawthurai sp. nov.
Mt. Popa Bent-toed Gecko
Cyrtodactylus fea Wood et al., 2012:995; 
Agarwal et al., 2014:147; Brennan et al., 2017:3.


Figure 8: Type specimens of Cyrtodactylus myintkyawthurai sp. nov. from the type locality of Taung Twin Chaung camp, Mt. Popa, Kyauk-pa-taung Township, Mandalay Region, Myanmar.
 (A) Adult male holotype LSUHC 13808. (B) Adult male paratype LSUHC 13807. (C) Subadult male paratype 13806. (D) Juvenile male paratype LSUHC 13809.
Photos by L. Lee Grismer.

Diagnosis. Cyrtodactylus myintkyawthurai sp. nov. differs from other species in the peguensis group by having the unique combination of six or seven supralabials and six or seven infralabials; 28–33 paravertebral tubercles; 17–23 longitudinal rows of body tubercles; 32–36 ventral scales; 17–19 subdigital lamellae on the fourth toe; 12–20 femoral pores in males; 7–9 precloacal pores in males; two rows of post-precloacal scales; raised, moderately to strongly keeled body tubercles; and a maximum SVL of 75.1 mm.

Distribution. Cmyintkyawthurai sp. nov. ranges throughout Mt. Popa, Mandalay Region and the central section of the Bago Yoma Range, Bago Region (Fig. 2).

Etymology. The specific epithet, myintkyawthurai, is a patronym honoring Myint Kyaw Thura for his contributions to the study of herpetology in Myanmar, his discovery of several new species, and his collaboration with foreign researchers.

Natural History. At both Mt. Popa and in the central Bago Yoma Range, C. myintkyawthurai sp. nov. occurs in hilly regions covered in deciduous dipterocarp forest up to 978 m in elevation (Fig. 9). The Mt. Popa specimens were collected at night from 0.05 to 1 m above the ground on rocks, the trunks of small trees, on leaves or on the ground amongst small rocks.



Conclusions: 
A phylogenetic taxonomy of species in the Cyrtodactylus peguensis species group from the Ayeyarwady Basin of Myanmar recovers at least seven species, four of which are undescribed. Three species, including C. peguensis occur in the low hills of the Bago Yoma mountain range one of which, C. meersi sp. nov., is syntopic with C. peguensis. As more lowland hilly areas associated with the Ayeyarwady Basin are surveyed, more new species of this group are likely to be discovered. These discoveries continue the recent surge of descriptions of new species of Cyrtodactylus that are being discovered in Myanmar.


L. Lee Grismer​, Perry L. Wood Jr, Evan S.H. Quah, Matthew L. Murdoch, Marta S. Grismer, Mark W. Herr, Robert E. Espinoza, Rafe M. Brown and Aung Lin. 2018.  A Phylogenetic Ttaxonomy of the Cyrtodactylus peguensis Group (Reptilia: Squamata: Gekkonidae) with Descriptions of Two New Species from Myanmar.  PeerJ. 6:e5575. DOI: 10.7717/peerj.5575

[Mammalogy • 2018] Diversity, Morphological Phylogeny, and Distribution of Bats of the Genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

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Molossus molossus (Pallas, 1766) 
[Velvety Free-tailed Bat] in Rio Doce State Park, Brazil

in Loureiro, Gregorin & Perini, 2018
 Photo: Marco A. R. Mello. instagram.com/marmello77 

Tenuous descriptions of many species and subspecies of mastiff bats make the taxonomy of Molossus E. Geoffroy, 1805 confusing and unstable. Molossus is one of the most diverse genera of free tailed bats in the pantropical family Molossidae Gervais, 1856. Given their impressive variation due to geography, sex, and ontogeny, and incomplete knowledge about species boundaries, a comprehensive taxonomic revision of the genus is needed. In addition, the level of genetic divergence, even among morphologically well-characterized species is low, often making diagnosis of groups difficult and likely resulting in an underestimation of the number of species. Brazil has a wide territory harboring many different physiognomies, but with no study focusing on the morphological variation and taxonomy of Molossus available. Therefore, we have analyzed qualitative and quantitative characters from 493 specimens belonging to nine species of Molossus, and conducted a wide comparative morphological analysis of the species occurring in Brazil. In addition, we propose a hypothesis of phylogenetic relationships within Molossus based on morphology, establishing the morphological characters for diagnosis and identification of species, and update the geographic distribution of Molossus species in Brazil, with range extensions for four taxa. Six species, Molossus rufus E. Geoffroy, 1805, Molossus molossus (Pallas, 1776), Molossus coibensis Allen, 1904, Molossus aztecus Saussure, 1860, Molossus currentium Thomas, 1901, and Molossus pretiosus Miller, 1902 occur in Brazil. We bring support for the synonymy of Molossus bondae Allen, 1904 with M. currentium, as suggested by several authors.

KEYWORDS: Brazil, Mastiff bats, morphology, identification key, phylogenetic relationships.


Livia Oliveira Loureiro, Renato Gregorin and Fernando Araujo Perini. 2018. Diversity, Morphological Phylogeny, and Distribution of Bats of the Genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil. ZOOSYSTEMA. 40(18); 425-452.  

[Invertebrate • 2018] Ceratotarsonemus amazonicus • Review of the Genus Ceratotarsonemus De Leon, 1956 (Acari: Prostigmata: Tarsonemidae), with Description of A New Species from the Amazon Forest

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Ceratotarsonemus amazonicus 
Rezende, Lofego, Gulbronson,  Bauchan &  Ochoa, 2018


Abstract
The genus Ceratotarsonemus De Leon (Acari: Prostigmata: Tarsonemidae) is reviewed here, with the addition of an updated key for the genus. Ceratotarsonemus amazonicus, sp. nov., found in the Brazilian Amazon rainforest, is described. Phase contrast (PC), differential interference contrast (DIC), low temperature scanning electron microscopy (LT-SEM) and confocal microscopy (CLSM) micrographs are provided. Biological and ecological aspects about the role of this species in its ecosystem are also discussed.

Keywords: Acari, diversity, fauna, Heterostigmatina, mite, taxonomy


José Marcos Rezende, Antonio Carlos Lofego, Connor J. Gulbronson, Gary Bauchan and Ronald Ochoa. 2018. Review of the Genus Ceratotarsonemus De Leon, 1956 (Acari: Prostigmata: Tarsonemidae), with Description of A New Species from the Amazon Forest. Zootaxa. 4483(2); 271–294. DOI: 10.11646/zootaxa.4483.2.3

[Ichthyology • 2018] Phylogenetic Classification of Extant Genera of Fishes of the Order Cypriniformes (Teleostei: Ostariophysi)

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 Fishes of the Order Cypriniformes 

Tan & Armbruster, 2018. 

Abstract
The order Cypriniformes is the most diverse order of freshwater fishes. Recent phylogenetic studies have approached a consensus on the phylogenetic relationships of Cypriniformes and proposed a new phylogenetic classification of family-level groupings in Cypriniformes. The lack of a reference for the placement of genera amongst families has hampered the adoption of this phylogenetic classification more widely. We herein provide an updated compilation of the membership of genera to suprageneric taxa based on the latest phylogenetic classifications. We propose a new taxon: subfamily Esominae within Danionidae, for the genus Esomus.

Keywords: Pisces, Cyprinidae, Cobitoidei, Cyprinoidei, carps, minnows


Milton Tan and Jonathan W. Armbruster. 2018. Phylogenetic Classification of Extant Genera of Fishes of the Order Cypriniformes (Teleostei: Ostariophysi). Zootaxa. 4476(1); 6–39.  DOI: 10.11646/zootaxa.4476.1.4  


[Herpetology • 2018] Adelophryne michelin • Diversity of Miniaturized Frogs of the Genus Adelophryne (Anura: Eleutherodactylidae: Phyzelaphryninae): A New Species from the Atlantic Forest of northeast Brazil.

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Adelophryne michelin  
Lourenço-de-Moraes, Dias, Mira-Mendes, Oliveira, Barth, Ruas, Vences, Solé & Bastos, 2018


Abstract
The number of species of frogs in the South American genus Adelophryne has increased in recent years, and it has become apparent that this group contains a substantial amount of undescribed diversity. Currently the genus contains nine described species and five candidate species. Here we describe the tenth species of the genus Adelophryne from the municipality of Igrapiúna, southern Bahia state, Brazil. The new species is characterized by its small body size, indistinct tympanum, and two phalanges in the finger IV. The species of the genus are distributed in three groups, Northern Amazonia Clade, Northern Atlantic Forest Clade and Southern Atlantic Forest Clade. The new species is phylogenetically related to species of the Northern Atlantic Forest Clade of Adelophryne and restricted to forested habitat, as typical for other Adelophryne. The species is restricted to the pristine forests in the type locality, and we consider its conservation status as Near Threatened. New morphological and molecular data of other Adelophryne species are presented, extending the distribution of Adelophryne sp. 2, Adelophryne sp. 4, Adelophryne mucronata and Adelophryne glandulata. However, a more comprehensive revision of the diversity and phylogenetic position of most Adelophryne species is needed, and the evolutionary relationships of A. meridionalis and A. pachydactyla remain unknown.




Adelophryne michelin sp. nov.
Adelophryne sp. (Mira-Mendes et al. [2018])

Etymology: The name “michelin” honors the Reserva Ecológica Michelin that has been supporting our researches for more than 10 years in the municipality of Igrapiúna, Bahia. The name is used as an invariable noun in apposition to the generic name.

Common name: Michelin Flea Frog or rãzinha-pulga-da-Michelin (in Portuguese).

Diagnosis: The new species is included in the subfamily Phyzelaphryninae because of the molecular evidence and by the presence of apically pointed digits; its leaf litter habitat; its terminal digits either barely or not expanded, and the SVL not exceeding 23 mm in SVL. In addition to the results of molecular analysis, the generic assignment of Adelophryne michelin sp. nov. is based on the possession of a head narrower than body, cranial crests absent, small size, with subdigital pad and mucronate tip on the fingers and toes, toes III and IV with discs and mucronate tips, and terminal phalanges of toes and fingers T-shaped.

The new species can be distinguished from species in the genus Phyzelaphryne by the absence of subarticular tubercles on fingers, for presenting indistinct tympanum, and reduction of the phalanges in the Finger IV. Phyzelaphryne has subarticular tubercles, distinct tympanum and no reduction of the phalanges.

The new taxon is diagnosed by the following combination of character states: (1) snout–vent length smaller than 11.5 mm (males 7.6–9.1 mm, N = 7; females 10.0–11.4 mm, N = 12); (2) tympanum indistinct without visible membrane; (3) tympanic annulus absent; (4) dentigerous processes of vomers present; (5) fingers without terminal discs, with mucronate tips, terminal phalanges T-shaped; (6) toes with terminal discs or circumferential grooves and mucronate tips; (7) terminal phalanges of toes T-shaped and sharply reduced; (8) Finger I shorter than Finger II; (9) Finger IV with two phalanges; (10) Toe III longer than Toe V; (11) subarticular tubercles absent on the fingers and toes (subdigital pads present); (12) belly skin smooth; (13) dorsum skin smooth; (14) anal flap absent.


Fig 4. Adult individuals of Adelophryne michelin sp. nov. in life (A) female paratype MBML 10498 and (B) paratype but not identified. Individual (A) showing an unusual bluish coloration and (B) showing common coloration.

Fig 5. Phylogenetic relationship of genus Adelophryne through 16S mitochondrial rRNA fragment gene (798 bp). Bayesian Posterior Probabilities and Maximum Likehood Bootstrap values are indicated above and below the branches. Asterisk = ≥ 0.99 and values below 0.50 are not shown (see methods for analysis details).
Abbreviations are: NAFC = Northern Atlantic Forest Clade; NAMC = Northern Amazonia Clade and SAFC = Southern Atlantic Forest Clade representing the clades proposed by Fouquet et al. [9]. The paratype of Adelophryne glandulata (MZUESC 12180) has number MH304347 in the tree. Photos not to scale.



Geographic distribution: Adelophryne michelin sp. nov. is known only from the type locality, at the Reserva Ecológica Michelin (REM), municipality of Igrapiúna, Bahia—Brazil (Fig 6).

Natural history, ecology and status conservation: Adelophryne michelin sp. nov. occurs in the leaf litter of primary forest. Two large ovarian eggs (2.0 mm) were found in one female of Adelophryne michelin sp. nov. (ZUFG 10697). We dissected five specimens of Adelophryne michelin sp. nov. one specimens there was nothing (ZUFG 10696) and four specimens revealed ants in their stomachs (ZUFG 10695 and 10697, MZUESC 17506, MBML10498). Beetles were found in stomachs of A. glandulata and ants were also found in A. glandulata [8] in A. gutturosa [5] and in A. mucronata [6]. We recorded a new population of A. mucronata and A. sp. 2 (sensu Fouquet et al. [9]), both species living sympatrically and syntopically with A. michelin sp. nov. in the REM.

Adelophryne michelin sp. nov has only been recorded at the type locality, in the Atlantic Forest biome of southeast Bahia, being restricted to well preserved forests. Based on the forest remnants size of landscape its area of occupancy is <500 km². As such, this new species can be included under criterion B2a of IUCN Red List [28]. Because we do not have data on habitat decline [11] or population data, we felt unable to fit the species into a threat category given that at least two of three conditions of criterion "B" need to be fulfilled for including a species into a threat category. Thus, we suggest that Adelophryne michelin sp. nov. should be listed as Near Threatened (NT) under the criterion B2a.


 Ricardo Lourenço-de-Moraes, Iuri R. Dias, Caio V. Mira-Mendes, Renan M. de Oliveira, Adriane Barth, Danilo S. Ruas, Miguel Vences, Mirco Solé and Rogério P. Bastos. 2018. Diversity of Miniaturized Frogs of the Genus Adelophryne (Anura: Eleutherodactylidae): A New Species from the Atlantic Forest of northeast Brazil.   PLoS ONE. 13(9): e0201781.  DOI:  10.1371/journal.pone.0201781

[Botany • 2018] Scleria aureovillosa (Cyperaceae) • A New Species of Scleria P.J.Bergius from North-Eastern Thailand

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Scleria aureovillosa Kiaosanthie & K.Wangwasit

in Kiaosanthie, Wangwasit & Chaisongkram, 2018. 
กกลูกขนทอง  || DOI: 10.20531/tfb.2018.46.2.01 

ABSTRACT
Scleria aureovillosa Kiaosanthie & K.Wangwasit, a new species of Cyperaceae from North-Eastern Thailand, is described and illustrated. It is closely related to S. benthamii C.B.Clarke but differs in the leaf and culm surfaces, culm shape, the absence of wings at the leaf sheath, contraligule features, nutlet morphology and micromorphology, and leaf and culm anatomy. An emended section of the key to the species in the Flora of Thailand account of Scleria is provided.

KEYWORDS:  anatomy, nutlet, Scleria aureovillosa, taxonomy, Thailand


Figure 2. Scleria aureovillosa Kiaosanthie & K.Wangwasit.
A‒B. part of inflorescence; C. nutlet; D. disk 3-lobed; E. rhizome; F. habitat.

Scleria aureovillosa Kiaosanthie & K.Wangwasit, sp. nov.

Similar to Scleria benthamii C.B.Clarke but differs in having trigonous culms (vs triquetrous in S. benthamii), an obtuse contraligule (vs rounded to truncate) and nutlets 2.1‒2.5 mm long (vs 2.6‒2.9 mmlong), subglobose to globose, terete, with a black, apiculate apex (vs ovoid, subterete to trigonous and obtuse apex) (Fig. 3 & Table 1). 
Type: Thailand, Loei, Phu Rua, 1,155 m, 12 Nov. 2012, Kiaosanthie WK 0152012 (holotype BKF [194620!]; isotypes KKU!, QBG!) (Figs. 1, 2 & 3A‒C).


Ecology.― Growing in seasonally wet, open grassy places on hillsides and on sandy soil; 100‒1155 m alt.

Vernacular.― Kok luk khon thong (กกลูกขนทอง).The Thai name translates as ‘sedge with golden hairs on the nutlet surface’.

Etymology.― The specific epithet of this new species is taken from the Latin aureus and villus, which refers to the distinctive feature of the species having golden villous hairs on the mature nutlet surface.


Wipawan Kiaosanthie, Kamolhathai Wangwasit and Wanwipha Chaisongkram. 2018. A New Species of Scleria P.J.Bergius (Cyperaceae) from North-Eastern Thailand. THAI FOREST BULLETIN (BOTANY). 46(2); 113–122.  DOI: 10.20531/tfb.2018.46.2.01

    

[Herpetology • 2018] Hemiphyllodactylus ywanganensis & H. uga • Two More New Species of Hemiphyllodactylus Bleeker (Squamata: Gekkonidae) from the Shan Hills of eastern Myanmar

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 (A) Hemiphyllodactylus ywanganensis &  (B and C) H. uga


Grismer, Wood, Zug, Thura, Grismer, Murdoch, Quah & Lin, 2018

Abstract 
An integrative phylogenetic analysis recovers two new species of the gekkonid genus Hemiphyllodactylus (Bleeker) from the Shan Hills of eastern Myanmar. Hemiphyllodactylus ywanganensis sp. nov. and H. uga sp. nov. are nested within the eastern Myanmar clade of a previous genus-wide phylogenetic analysis and form a more exclusive monophyletic group with H. linnwayensis. These species differ from each other and all other Hemiphyllodactylus in having unique combinations of character states involving postmental and subcaudal scale morphology; maximum SVL; digital formulae; numbers of chin scales, circumnasals, intersupranasals (=postrostrals), labials, longitudinally arranged dorsal and ventral scales, and pore-bearing femoroprecloacal scales; as well as subtle differences in coloration and pattern. The phylogenetic affinities of the eastern Myanmar clade are similar to those of an endemic clade of Cyrtodactylus from the Shan Hills in that both are more closely related to Indochinese taxa east of Myanmar as opposed to other Indo-Burmese species. The discovery of these new species underscores the underappreciated herpetological diversity of limestone ecosystems as well as the remote nature of the rugged uplands of the Shan Hills and emphasizes the need for continued field work in this region. 

Key words: Indochina, systematics, new species, Gekkonidae, Burma

FIGURE 4. A. Adult female paratype (LSUHC 13138) of Hemiphyllodactylus ywanganensis sp. nov. from 2.7 km southwest of Ywangan, Ywangan Township, Taunggyi District, Shan State, Myanmar
(Photo by L. L. Grismer).
 B and C: Adult male holotype (USNM 570733) and adult female paratype (USNM 570734) of Hemiphyllodactylus uga sp. nov., respectively, from the Pyin Oo Lwin, Kandawgyi National Gardens, Pyin Oo Lwin, Mandalay Region, Myanmar
(Photos by G. R. Zug). 

Hemiphyllodactylus ywanganensis sp. nov. 
Ywangan Slender Gecko

Etymology. The specific epithet, ywanganensis, is a noun in apposition in reference to the type locality being near the town of Ywangan, Shan State.


Hemiphyllodactylus uga sp. nov. 
Uga’s Slender Gecko  
Hemphyllodactylus sp. nov. 8. Grismer et al. 2013:872, Grismer et al. 2014a:67, Grismer et al. 2014b:490, Ngo et al. 2014:541, Grismer et al. 2015:861
Hemiphyllodatylus cf. linnwayensis. Grismer et al. 2017b:31

Etymology. The specific name recognizes and honors the late U Uga. He was a conservationist and a former director of the Nature and Wildlife Conservation Division (NWCD), Myanmar Forestry Department. He encouraged Joseph B. Slowinski and George R. Zug to do an all-country herpetofaunal survey and established the administrative protocol to establish and support survey teams of NWCD wildlife rangers. These teams working independently and with CAS and USNM collaborators were the essential factor for the high productivity and success of the Myanmar Herpetological Survey (MHS).


 L. L. Grismer, Perry L. Wood, Jr., George R. Zug, Myint K. Thura, Marta S. Grismer, M. L. Murdoch, Evan S. H. Quah and Aung Lin. 2018. Two More New Species of Hemiphyllodactylus Bleeker (Squamata: Gekkonidae) from the Shan Hills of eastern Myanmar (Burma). Zootaxa. 4483(2); 295–316. DOI:  10.11646/zootaxa.4483.2.4

[Entomology • 2018] A Contribution to the Systematics of the Genus Manota Williston (Diptera: Mycetophilidae) in Brazil

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Manota sp.

Kurina, Hippa & Souza Amorim, 2018. 

Abstract
A total of 286 male specimens of Manota from 38 different collecting sites in the Brazilian Atlantic Forest were analysed. They belong to 32 different species, including 20 described as new to science and 12 recognized as previously described species. The new species are Manota abbreviata sp. n., M. atlantica sp. n., M.carioca sp. n., M. cavata sp. n., M. hirta sp. n., M. lamasi sp. n., M. lanei sp. n., M. nordestina sp. n., M. oliveirai sp. n., M. paniculata sp. n., M. papaveroi sp. n., M. periotoi sp. n., M. perparva sp. n., M. pseudoiota sp. n., M. rostrata sp. n., M. sanctavirginae sp. n., M. securiculata sp.n., M. silvai sp. n., M. tavaresi sp. n. and M. unispinata sp. n. The taxonomic context of the newly described species is discussed. Manota palpalis Lane, 1948, the type of which is considered lost, is redescribed and discussed, based on the original description, the original illustrations, and the type-locality. Our specimens of the previously described species belong to M. aligera Hippa, Kurina & Sääksjärvi, 2017, M.anfracta Hippa & Kurina, 2013, M. appendiculata Hippa & Kurina, 2013, M. caribica Jaschhof & Hippa, 2005, M. diversiseta Jaschhof & Hippa, 2005, M. micula Hippa & Kurina, 2013, M. panda Hippa & Kurina, 2013, M. pustulosa Hippa, Kurina & Sääksjärvi, 2017, M. quantula Hippa & Kurina, 2013, M. serrulata Hippa, Kurina & Sääksjärvi, 2017 and M. subaristata Kurina, Hippa & Amorim, 2017. Among the species dealt with here, ten have a wide distribution in South America or the Neotropics, six are known from only a single site, nine are widespread along the Atlantic Forest, and seven are known only from southern Brazil/northwestern Argentina. A discrepancy between the distribution patterns of Manota species and the general areas of endemism known for flies in the Atlantic Forest is discussed, and a non-destructive sequencing reverse workflow protocol for Manota specimens proposed.

        Including the species described here, the Neotropical region closely approaches the Oriental region in terms of the number of described species (92 and 102, respectively), while the genus now includes 300 species worldwide.

Keywords: Diptera, Sciaroidea, Neotropical region, Atlantic Forests, taxonomy, new species


Olavi Kurina, Heikki Hippa and Dalton de Souza Amorim. 2018. A Contribution to the Systematics of the Genus Manota Williston (Diptera: Mycetophilidae) in Brazil. Zootaxa. 4472(1); 1–59.  DOI:  10.11646/zootaxa.4472.1.1
Scientists discovered 20 new gnat species in Brazil 
bit.ly/2OLXD2c via @EurekAlert

 Olavi Kurina, Heikki Hippa and Dalton de Souza Amorim. 2017. New species and new records of Manota Williston from Colombia, Brazilian Amazonia, and Costa Rica (Diptera, Mycetophilidae). ZooKeys. 668: 83-105.  DOI:  10.3897/zookeys.668.11350

[Chilopoda • 2018] Scolopendra paradoxa • A Phylogenetic Approach to the Philippines Endemic Centipedes of the Genus Scolopendra Linnaeus, 1758 (Scolopendromorpha, Scolopendridae), with the Description of A New Species

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Scolopendra paradoxa Doménech

in Doménech, Barbera & Larriba, 2018

Abstract
The genus Scolopendra Linnaeus, 1758 is represented in the Philippines’ fauna by five species, two of which are endemic. Mitochondrial DNA sequences of gene cytochrome c oxidase subunit I (COI) were obtained from six Scolopendra specimens belonging to two endemic species and a new one, described here as Scolopendra paradoxa Doménech sp. nov. These sequences were analyzed together with another forty-one sequences from GenBank, including additional species of Scolopendra and a few representatives of other Scolopendridae genera. Phylogenetic trees inferred from the COI analysis using maximum likelihood and neighbor joining showed the three Philippines Scolopendra endemic species as a polyphyletic group coherent with their respective morphologies, although the position of S. spinosissima Kraepelin, 1903 varied within the obtained trees. Species delimitation based on standard external morphological characters was also concordant with the observed genetic distances, monophyly and node support, confirming S. subcrustalis Kronmüller, 2009 and S. paradoxa sp. nov. as separate species also at the molecular level, while only the position of S. spinosissima could not be properly established with any of the statistical methods used. In addition, the male genitalia of the three studied species were found to lack gonopods and a penis. Remarks on the ultimate legs prefemoral spinous formula of S. spinosissima plus a key to the species of the genus Scolopendra in the Philippines are provided.

Keywords: Myriapoda, Chilopoda, scolopendromorph, Scolopendra paradoxaScolopendra spinosissimaScolopendra subcrustalis, barcode, cytochrome oxidase I


FIGURE 13. Scolopendra paradoxa sp. nov. specimen found underwater in a Mindoro's forest stream. Observe that the specimen is partial covered by rocks and river’s sand, showing probably an attempt of underwater concealment, which has been previously described only in S. cataracta(Siriwut et al. 2016).

Family Scolopendridae Newport, 1844 
Subfamily Scolopendrinae Kraepelin, 1903 

Genus Scolopendra Linnaeus, 1758 
Scolopendra paradoxa Doménech sp. nov. 
....

Etymology. From “paradoxon”, meaning contradiction, because the new species’ author initially identified this new taxon as a color variant of S. spinosissima. Nevertheless, the genetic divergence between these two species contrasted with earlier identifications. 

Suggested common name. Philippine’s cyan leg centipede.


Carles Doménech, Victor M. Barbera and Eduardo Larriba. 2018. A Phylogenetic Approach to the Philippines Endemic Centipedes of the Genus ScolopendraLinnaeus, 1758 (Scolopendromorpha, Scolopendridae), with the Description of A New Species. Zootaxa. 4483(3); 401–427.  DOI: 10.11646/zootaxa.4483.3.1

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