A likely new natural hybrid form of Cuora serrata (Cuora picturata x Cuora mouhotii obsti) and its presence in the wild in Phu Yen province, Vietnam

Similar documents
Transfer of Indochinese Box Turtle Cuora galbinifrons from Appendix II to Appendix I. Proponent: Viet Nam. Ref. CoP16 Prop. 33

Cuora mouhotii (Gray 1862) Keeled Box Turtle

CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA

Original language: English CoP18 Prop. 33 CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA

Freshwater turtle trade in Hainan and suggestions for effective management

DNA evidence for the hybridization of wild turtles in Taiwan: possible genetic pollution from trade animals

Ecomorphological correlates of microhabitat selection in two sympatric Asian box turtle species (Geoemydidae: Cuora)

STUDBOOK BREEDING PROGRAMME

Natural history observations on the endangered turtle Geoemyda spengleri in Tay Yen Tu Nature Reserve (Vietnam), with notes on other sympatric species

Securing Endangered Tortoises and Freshwater Turtles in the Indo-Burma Region

CHELONIAN CONSERVATION AND BIOLOGY International Journal of Turtle and Tortoise Research

Transfer of the Family Platysternidae from Appendix II to Appendix I. Proponent: United States of America and Viet Nam. Ref. CoP16 Prop.

Interspecific hybridization between Mauremys reevesii and Mauremys sinensis: Evidence from morphology and DNA sequence data

Inclusion of Ryukyu Black-breasted Leaf Turtle Geoemyda japonica in Appendix II with a zero annual export quota for wild specimens

SPECIMEN SPECIMEN. For further information, contact your local Fisheries office or:

This publication was made possible through financial assistance provided by the Western Pacific Regional Fishery Management Council (WPRFMC)

CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II

LESSON TWO: Turtle Physical Features and Habitat PHASE LEARNING SEQUENCE ACTIVITY RESOURCES Engage

Article. Museum of Vertebrate Zoology; University of California, Berkeley; Berkeley, CA 94720; USA. 2

University of Canberra. This thesis is available in print format from the University of Canberra Library.

Status: IUCN: Data Deficient, CITES: Appendix I (international trade and transport prohibited) FR: tortue à dos plat ESP: tortuga plana de Australia

Phylogenetic Relationships of the Asian Box Turtles of the Genus Cuora sensu lato (Reptilia: Bataguridae) Inferred from Mitochondrial DNA Sequences

Report to TRAFFIC Compiled Notes on the Wildlife Trade in Vietnam June 1 September 30, 2000

CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA

This publication was made possible through financial assistance provided by the Western Pacific Regional Fishery Management Council (WPRFMC)

click for previous page SEA TURTLES

METHODS RESULTS. STUART AND THORBJAKNARSON - Prioritization of Asian Turtle Conservation 643

Indochinese Rat Snake Non Venomous Not Dangerous

DESERT TORTOISE SIGN RECOGNITION INITIAL REQUIREMENTS DESERT TORTOISE SIGN RECOGNITION. Find Sign in the Open INITIAL REQUIREMENTS.

Reptiles. Ectothermic vertebrates Very successful Have scales and toenails Amniotes (lay eggs with yolk on land) Made up of 4 orders:

Reptile Identification Guide

Bew *Blue-Eyed White* Surface color: Pure White Undercolor: Pure White

Outline. Identifying Idaho Amphibians and Reptiles

First Record of Lygosoma angeli (Smith, 1937) (Reptilia: Squamata: Scincidae) in Thailand with Notes on Other Specimens from Laos

Sea Turtle, Terrapin or Tortoise?

A revision of Testudo tungia Yeh, 1963 from the Lower Pleistocene Gigantopithecus cave, Liucheng, Guangxi Province, China

Golden-spectacled Warblers

RATE OF SCUTE ANNULI DEPOSITION OF EASTERN BOX TURTLES (TERRAPENE CAROLINA CAROLINA) HELD IN CAPTIVITY AND IN THEIR NATURAL HABITAT

TEXAS TURTLE REGULATIONS

TURTLE AND TORTOISE NEWSLETTER The Newsletter of Chelonian Conservationists and Biologists

CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II

Madagascar Spider Tortoise Updated: January 12, 2019

JoJoKeKe s Herpetology Exam

CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA

Parthenogenesis in Varanus ornatus, the Ornate Nile Monitor.

Think smart: Putting confiscated wildlife legally back into the trade compromises the efforts of law enforcement and puts wildlife at risk

Promotion of underutilized indigenous food resources for food security and nutrition in Asia and the Pacific

2015 Artikel. article Online veröffentlicht / published online: Deichsel, G., U. Schulte and J. Beninde

18 August Puerto Rican Crested Toad Dustin Smith, North Carolina Zoological Park

from Lao People s Democratic Republic

Proponent: Switzerland, as Depositary Government, at the request of the Animals Committee (prepared by New Zealand)

*Using the 2018 List. Use the image below to answer question 6.

AUSTRALIAN MUSEUM SCIENTIFIC PUBLICATIONS

A characterisation for markings of the smooth snake (Coronella austriaca)

Peng GUO 1, 2*, Qin LIU 1, 2, Jiatang LI 3, Guanghui ZHONG 2, Yueying CHEN 3 and Yuezhao WANG Introduction. 2. Material and Methods

Cuora flavomarginata (Gray 1863) Yellow-Margined Box Turtle

APPLICATION OF BODY CONDITION INDICES FOR LEOPARD TORTOISES (GEOCHELONE PARDALIS)

Who Really Owns the Beach? The Competition Between Sea Turtles and the Coast Renee C. Cohen

ACTIVITY #2: TURTLE IDENTIFICATION

426 Common Chaffinch. Put your logo here. COMMON CHAFFINCH (Fringilla coelebs) IDENTIFICATION

Eating pangolins to extinction

沖縄島国場川水系饒波川から採集されたクサガメ, ヤエヤマイシガメおよび両種の雑種と推定されるカメの記録.

Northern Copperhead Updated: April 8, 2018

NATIONAL HERTETOLOGY List posted o n under Event Based upon information at

S1 Materials; Slide Specimen Photos The Cellular Expression and Genetics of Purple Body (Pb) in the Ocular Media of the Guppy Poecilia reticulata

People around the world should be striving to preserve a healthy environment for both humans and

Wild Fur Identification. an identification aid for Lynx species fur

W. E. CASTLE C. C. LITTLE. Castle, W. E., and C. C. Little On a modified Mendelian ratio among yellow mice. Science, N.S., 32:

Great Science Adventures Lesson 12

Progress Report. Okavango Crocodile Monitoring Programme.

Molecular Systematics of Old World Stripe-Necked Turtles (Testudines: Mauremys)

Taxonomy. Chapter 20. Evolutionary Development Diagram. I. Evolution 2/24/11. Kingdom - Animalia Phylum - Chordata Class Reptilia.

How to sex and age Grey Partridges (Perdix perdix)

2. SANCTUARIES: Over 50% of Cambodia s wild crocodiles are in sites that are effectively protected and managed as crocodile sanctuaries.

Captive Versus Wild. My last few papers have been on the subject of wild-caught versus captive-bred

Class Reptilia Testudines Squamata Crocodilia Sphenodontia

Inheritance of the king coat colour pattern in cheetahs Acinonyx jubatus

Breeding Spangles by Ghalib Al-Nasser

CAPTIVE HUSBANDRY AND REPRODUCTION OF THE LEOPARD SNAKE ELAPHE SITULA

B-Division Herpetology Test. By: Brooke Diamond

Turtles And Tortoises For Dummies By Liz Palika READ ONLINE

UKRAINIAN CLAY (Ukrainskaya glinistaya)

THE LAST CHANCE FOR THE GREEN-NECKED PEAFOWL (Pavo muticus)? By: Wolfgang Mennig, WPA-Germany

A description of an Indo-Chinese rat snake (Ptyas korros [Schlegel, 1837]) clutch, with notes on an instance of twinning

Legal Supplement Part B Vol. 53, No th March, NOTICE THE ENVIRONMENTALLY SENSITIVE SPECIES (GREEN TURTLE) NOTICE, 2014

Three snakes from coastal habitats at Pulau Sugi, Riau Islands, Indonesia

Introduction to phylogenetic trees and tree-thinking Copyright 2005, D. A. Baum (Free use for non-commercial educational pruposes)

examnined when three weeks old. Not one of the eyes showed

The tailed frog has been found from sea level to near timberline ( m; Province of BC 1999).

The average live weight of males is 7-9 kg and that of females is 5-7 kg. The 60-day-old goslings weigh kg. Egg production is eggs;

The family Gnaphosidae is a large family

Tridacna maxima. Common Names. Natural Habitat. Geographic Range and Status. Roding (1798a)

SHEEP SIRE REFERENCING SCHEMES - NEW OPPORTUNITIES FOR PEDIGREE BREEDERS AND LAMB PRODUCERS a. G. Simm and N.R. Wray

Lower Cretaceous Kwanmon Group, Northern Kyushu

Marine Reptiles. Four types of marine reptiles exist today: 1. Sea Turtles 2. Sea Snakes 3. Marine Iguana 4. Saltwater Crocodile

Afring News. An electronic journal published by SAFRING, Animal Demography Unit at the University of Cape Town

6. The lifetime Darwinian fitness of one organism is greater than that of another organism if: A. it lives longer than the other B. it is able to outc

Estimating radionuclide transfer to reptiles

SEA TURTLE CHARACTERISTICS

The Red-Eared Slider (Trachemys scripta elegans) In Singapore. Abigayle Ng Pek Kaye, Ruth M. O Riordan, Neil F. Ramsay & Loke Ming Chou

Transcription:

Herpetology Notes, volume 9: 73-80 (2016) (published online on 01 March 2016) A likely new natural hybrid form of Cuora serrata (Cuora picturata x Cuora mouhotii obsti) and its presence in the wild in Phu Yen province, Vietnam Richard P.J.H. Struijk 1, * and Torsten E.G. Blanck 2 Cuora serrata was originally described as a subspecies of Cuora galbinifrons (Iverson and McCord, 1992) and later elevated to full species status (Obst and Fritz, 1997). However, shortly after, it was proven to be a hybrid (Parham et al., 2001). Based on the genetic fingerprints of specimens originating from the wild and the pet trade, C. serrata appears to be a hybrid of Cuora mouhotii x Cuora galbinifrons or Cuora mouhotii x Cuora bourreti (Stuart and Parham 2004; Shi et al., 2005). Cuora serrata is nowadays considered a collective noun for hybrids between members of the galbinifrons-complex and C. mouhotii sensu lato. Until recently, no records of hybridization between C. mouhotii and the third member of the galbinifrons-complex, Cuora picturata, were known and this species was long supposed to occur outside the natural range of C. mouhotii (Shi et al., 2005). However, C. picturata was recently discovered in the wild on the Langbian Plateau in the southern Vietnamese provinces of Khanh Hoa and Phu Yen (Ly et al., 2011; Van Ha and McCormack 2012; Nguyen and McCormack 2012). At the time, this record was about 300 km south of the most southern record of C. mouhotii in Vietnam s Quang Nam province (Ly et al., 2013). However, simultaneously, C. mouhotii was also discovered in this area and classified as the southern subspecies C. m. obsti (Ly et al., 2013). Shortly after, both C. m. obsti and C. picturata were found within only a few hundred meters of each other 1 RAVON Foundation (Reptile, Amphibian & Fish Conservation Netherlands), Natuurplaza, Toernooiveld1, 6525 ED Nijmegen, the Netherlands, 2 Cuora Conservation Center, 8530 Deutschlandsberg, Austria * Corresponding author e-mail: r.struijk@ravon.nl at Deo Ca Hon Nua Special Use Forest (SUF), Dong Hoa District, Phu Yen province (Vietnam) (Blanck and Braun, in prep). This demonstrates sympatric occurrence, making hybridization geographically feasible - as also speculated by Ly et al. (2013). Between 2011 and 2014 photos of nine C. serrata - like specimens with clear C. picturata resemblance appeared on Chinese online pet reptile fora. These animals consisted of one subadult and eight adults. All originated from the Chinese turtle trade, therefore lack any locality. In addition, on 18 August 2014 an adult female was encountered in Suoi Dua village, Sông Hinh district, Phu Yen province, Vietnam (Nguyen et al., in prep) (Fig. 1). It had recently been caught by local hunters in Song Hinh forest. Although this turtle was encountered in the local trade, the circumstances and detailed information given by the hunter that actually caught it, lend credence to the locality s accuracy. The female was sold to a trader for 85 who planned to sell it with profit. Cuora picturata is characterized by high domed carapace. It lacks dorsal and lateral keels and a mahogany brown-reddish dorsal band is present (Fig. 2). Sporadically this colouration tends toward dark purple brown. The plastron is horn coloured with large solid black markings on each scute (Fig. 2). The soft parts display a unique reticulated pattern. Head coloration is lime yellow and the irises display black markings surrounding the pupil, making the pupil seem as not roundish but usually somewhat star shaped. Such iris markings are typical and unique for C. picturata and do not appear in C. galbinifrons and C. bourreti (Lehr et al., 1998) nor do they usually occur in C. serrata specimens without C. picturata parentage. Cuora mouhotii is characterised by dorsal and ventral keels and serrated hind marginals. It is dorsally more

74 Richard P.J.H. Struijk & Torsten E.G. Blanck Figure 1. Wild caught likely hybrid (Cuora picturata x Cuora mouhutii obsti) from Suoi Dua village, Sông Hinh district, Phú Yên province, Vietnam 18-8-2014 (Photos by T.L. Nguyen). or less flattened and usually chestnut to caramel brown in colour (Fig. 2). From the lateral keels downwards a radiating black pattern often occurs on the costalia. The soft parts are dark grey, though the neck region and head may display pinkish to yellowish colour and be finely reticulated. Two subspecies are currently recognized which are basically distinguished by their shape (mouhotii being more elongated, obsti more rounded) and particularly by their plastral pattern (mouhotii usually shows black bar-like markings along the outer edges; obsti shows radiating black markings which often form triangles, frequently extending to the plastrons center and in most cases black gulars and partly black patterned humerals (Fig. 2)). For phenotypic comparisons of putative hybrids we obtained one to six photos for each of the ten specimens,

A likely new natural hybrid form of Cuora serrata and its presence in Vietnam 75 Figure 2. Dorsal and plastral views of Cuora picturata (top), Cuora mouhotii obsti (middle), Cuora mouhotii mouhotii (bottom) (Photos by R. Struijk and J. Stumpel). though quality and photo positioning differed per specimen. For all, the soft parts and carapace were visible in these photos, but plastron photos were only visible from seven. Each individual was compared to the most characteristic features of both suspected parental species (Table 1). Due to the fact of the limited number of photos it was impossible to analyse every feature for each specimen. In all ten specimens, multiple C. picturata features could be noticed, e.g. a high domed carapace, mahogany brown-reddish dorsal band, unique reticulations on the soft parts and yellowish top of head (Fig. 3). All nine specimens in which the eyes were visible in the photos, displayed black iris markings surrounding the pupils. Characteristics indicative of C. mouhotii parentage include serrated hind marginals and the presence of

76 Richard P.J.H. Struijk & Torsten E.G. Blanck Table 1. Characteristics for ten likely hybrids between Cuora picturata and Cuora mouhotii (obsti) (ad = adult; sub = subadult; + = present; ± = intermediary; - = absent;? = undeterminable from photos). S P E C I M E N 1 2 3 4 5 6 7 8 9 10 General data Year 2014 2014 2014 2014 2014 2014 2014 2011 2014 2013 Sex unknown unknown unknown female female unknown unknown female unknown unknown Stage adult adult adult adult adult subadult adult adult adult adult Locality data available yes no no no no no no no no no Photos available 4 6 1 6 4 4 6 6 3 1 C. picturata characteristics High domed carapace + + + + + + + + + + Black iris markings + + + +? + + + + + Reticulations soft parts + + + + + + + + + + Head (top) colour + ± + + + + + + ± + Mahogony dorsal band + +? + + + + + + + C. mouhotii characteristics Serrated hind marginals + ± + + + + + + +? Keels + + + ± + + + + + - Costal pattern + + + + + + + + + + Plastral pattern +?? + + + + + +? dorsal and lateral keels. Also, the black radiating costal pattern is present in all specimens (Fig. 3). Feature which in some cases are interpreted as intermediate are e.g. the keels, serrated hind marginal and the orange/ pink neck region, in one case extremely intense in color. Remarkably, in all cases the shape of the plastral pattern can possibly be linked to the subspecies Cuora mouhotii obsti. It displays a more radiating pattern, triangular shapes and the large percentage of the gular and intergular scutes that is covered by black markings. This pattern is typical for C. m. obsti and differs greatly from that of C. m. mouhotii (Fritz et al., 1998; Struijk et al., in prep.). Also the only (small) subadult specimen (6) displayed the very typical C. m. obsti plastral pattern. Based on the combination of multiple features for each specimen in the available photos, we believe that C. picturata genes are present in all ten specimens and C. mouhotii genes are present in at least nine specimens. In at least seven specimens indications of C. m. obsti genes are apparent. However, the analysis given is purely based on phenotypic features. In order to truly confirm the suspected parental lineages, genetic studies should be conducted, comparable to studies that revealed the galbinifrons- and bourreti lineage in other C. serrata (Parham et al., 2001; Shi et al., 2005). This might, however, prove difficult since, to the best of our knowledge, all specimens, if still alive, are within the trade or in private hobbyist collections. All ten specimens were encountered in turtle trade and locality data is only available for one. There is no real evidence to establish the origin of the other nine. Given the massive scale of farming in China, it can no longer be concluded that turtles sold at markets or within the trade in general, originate from the wild (Shi, 2002; Shi et al., 2004). Shi et al. (2005) provided evidence that C. serrata occurs in the wild but also stated that captive origin cannot be excluded. We agree that some captive breeding could have occurred, and in fact did occur at least once in Europe (Struijk and Blanck, 2015), however, we believe that an origin in the wild is most plausible for C. serrata in general, and this putative hybrid combination in particular. First, members of the galbinifrons-complex and C. mouhotii are of low economic value, highly susceptible to stress, very hard to breed and have a very low fecundity, especially C. picturata (Struijk, unpublished data; Blanck, unpublished data) - and do not fit into the Chinese turtle farm models. The presence of any species in a farm at the same time that it is abundant and cheaply available in the wild-collected trade, may simply mean that the farms recently stocked up on that species. Therefore, the presence in a farm does not in

A likely new natural hybrid form of Cuora serrata and its presence in Vietnam 77 Figure 3. Lateral views of likely hybrid (Cuora picturata x Cuora mouhotii obsti) (labelled as specimens 7 (top left), 9 (top right), 5 (bottom left) and 8 (bottom right) in table 2). (Photos by T. Blanck, T.M. Chan and Anonymous). any way imply that the species actually breeds in the farm. Even farm hatchlings may be captive hatched rather than captive bred, thus originating from gravid wild caught females. Shi et al. (2002, 2008) indicate the presence of one of the parental species, i.e. C. mouhotii, in large numbers in Chinese farms. However, these data were derived indirectly through questionnaires and it is questionable how reliable the identifications were (Shi et al. 2008). Zhou et al. (2008), who visited the farms themselves, could not find significant numbers of C. mouhotii (and C. galbinifrons) and no breeding success of this species at all. Zhou and Blanck visited dozens of farms within the last decade but only saw a handful of C. galbinifrons and C. mouhotii, all of which were in bad health and therefore in non-breeding condition. In Chinese turtle farms, many specimens are kept together in rather small enclosures, and their focus lies on species that either have a good reproduction rate (e.g., Mauremys reevesi) and/or a high economic value (e.g., Cuora trifasciata and Cuora cyclornata) or are reasonably hardy (e.g., Cuora flavomarginata). Outwardly this suggests captive production of Cuora picturata and Cuora mouhoti hybrids in Chinese farms is unlikely. Even farmers admit that their sporadic C. serrata all originate from the trade in wild caught turtles (Zhou, pers. comm.; Blanck, pers. obs.). Second, nearly all C. serrata show consistent natural growth which results in hard and smooth shells. The captive rearing of hatchlings and juveniles within the galbinifrons-complex, even by experienced keepers, often result in visible deformations in comparison to specimens from the wild (e.g. a more flattened shell or curled marginalia). If many C. serrata would be of captive origin, these deformaties might be expected. The ten picturata serrata specimens in this study all exhibit natural growth without any abnormalities that possibly could have been caused due to (improper) captive husbandry. Finally, and most convincingly, the only specimen with locality data originates from within the range

78 Richard P.J.H. Struijk & Torsten E.G. Blanck Figure 4. Plastral views of likely hybrid (Curora picturata x Cuora mouhotii obsti) (labelled as specimens 9 (top left), 8 (top right), 7 (bottom left) and 4 (bottom right) in table 2). (Photos by T. Blanck, T.M. Chan and Anonymous). of putative parentals in Vietnam. The locality of this specimen (Song Hinh forest) is located near the only very few C. picturata localities known to science, and in a zone where it occurs in sympatry with C. m. obsti. That characteristics of C. m. obsti are present in at least six specimens under examination here, lending further support to a wild origin. Plastral markings in galbinifrons serrata, which only sympatrically occur with C. m. mouhotii from further north in Vietnam and Southern China, show different markings (see Stuart and Parham, 2004; Struijk and Blanck, 2015). This said the possibility of captive origins for some specimens cannot be completely ruled out. The low economic value of parental species does not necessarily mean that crossings are of low value too. C. serrata initially was sold for the same prices as its parental species. After its description prices increased, but decreased sharply again when its hybrid status was revealed (Stuart and Parham 2004). However, due to the interest by Chinese hobbyists in hybrid specimens, prices started to increase again since 2005. Indonesian turtle traders were then offering C. serrata for prices which were threefold of that of C. galbinifrons, 330 and 110 per animal, respectively (Struijk pers. obs.). Nowadays prices reach up to approximately 1.000-2.000 with a maximum of 5.000 in September 2011 (Blanck, pers. obs.) and males are especially sought after. These data indicate that it could be commercially interesting to produce these hybrids in captivity. Theoretically this would probably be the best motivation to explain (some) captive origin. Still, we consider it highly unlikely that farmers have the capability to produce these extremely difficult to breed parental species in such numbers and rear hatchlings to adulthood. Despite thorough market surveys during the last two decades, no picturata serrata were seen in the Chinese trade even when large quantities of both parental species

A likely new natural hybrid form of Cuora serrata and its presence in Vietnam 79 Acknowledgements. We thank Dr. John B. Iverson (U.S.A.) for reviewing the manuscript. For providing photographs, we thank L. Nguyen (Vietnam), T.M. Chan China), B. Sturlese (Italy), J.B.G. Stumpel (Netherlands) and various anonymous photographers. We would also like to show our appreciation towards M. Klerks and J. Herder (both Netherlands) for photo editing and T. McCormack (UK) for providing the data on the Phu Yen specimen. References Figure 5. Plastral views of different Cuora serrata hybrids: Cuora galbinifrons x Cuora mouhotii mouhotii (top); Cuora bourreti x Cuora mouhotii mouhotii (bottom, see Struijk & Blanck, 2015) (Photos by T. Blanck and B. Sturlese). and other C. serrata varieties were being offered. It seems unlikely that hunters could recognize and ignore such hybrids, and instead collected pure specimens (until recently). Even the reasons behind the hybridization, and a possible increase in the detection rate of hybrids, are unknown. One hypothesis might be that the drastic decline in turtle densities reducing oppurtunities to find compatible counterparts for mating- as has been described in Teleostei (Crapon de Caprona and Fritzsch, 1984). Additional fieldwork and molecular studies may shed light on this question. Blanck, T., Braun, S. (in prep.): Scheue Schönheiten und Höhlenschildkröten auf Schildkrötensuche in Vietnam. Crapon de Caprona, M. D., Fritzsch, B. (1984): Interspecific fertile hybrids of haplochromine Cichlidae (Teleostei) and their possible importance for speciation. Nether. J. Zool. 4: 503-538. Fritz, U., Obst, F.J. (1997): Zum taxonomischen Status von Cuora galbinifrons serrata Iverson and McCord, 1992 und Pyxidea mouhotii (Gray, 1862) (Reptilia: Testudines: Bataguridae). Zool. Abh. Staatl. Mus. Tierk. Dresden 49: 261-279. Fiebig, J., Lehr, E. (2000). Haltung und Erstnachzucht der Bourret- Scharnierschildkröte Cuora galbinifrons bourreti Obst & Reinman, 1994, mit Anmerkungen zum Bedrohungsstatus. Salamandra 36 (3): 147-156 Fritz, U., Britta, A., Lehr, E. (1998). Eine neue Unterart der Dreikiel-Scharnierschildkrote, Pyxidea mouhotii (GRAY, 1862) (Reptilia: Testudines: Butaguridae). Staatsliches Museum für Tierkunde Dresden, Zoologische Abhandlungen 50(3): 33-43 Ha, H. Van, McCormack, T. (2012). Endemic Lesser Indochinese Box Turtle (Cuora picturata) under threat in Vietnam. Asian Turtle Program, asianturtleprogram.org (21-5-2012) Iverson, J.B., McCord, W.P. (1992): A new subspecies of Cuora galbinifrons (Testudines: Batagurinae) from Hainan Island, China. Proc. Biol. Soc. Washington 105: 433-439. Lehr, E., Fritz U., Obst, F.J. (1998). Die Unterarten von Cuora galbinifrons BOURRET 1939 (Reptilia: Testudines: Bataguridae). Zool. Abh. Staatl. Tierk. Dresden 50(1): 77-97 Ly, T., Hoang, H.D. & B.L. Stuart (2011). Market turtle mystery solved in Vietnam. Biological Conservation 144(5): 1767-1771 Nguyen, L. Van, McCormack, T. (2012): Field surveys for the endemic Lesser Indochinese Box Turtle (Cuora picturata) Khanh Hoa Province, Vietnam. asianturtleprogram.org (22-3- 2012). Nguyen, L., Tu, B.D., Mccormack, T., Le, M. (2015): Report on interview survey of threatened tortoise and freshwater turtles of Song Hinh and Dong Hoa district, Phu Yen province, Vietnam. In prep. Parham, J.F., W.B. Simison, K.H. Kozak, C.R. Feldman, Shi, H. (2001): New Chinese turtles: endangered or invalid? A reassessment of two species using mitochondrial DNA, allozyme electrophoresis and known-locality specimens. Animal Conservation 4: 357-367. Shi, H. (2002). Results of turtle market surveys in Chengdu and Kunming. Turtle and Tortoise Newsletter 6: 15-16 Shi, H., Fan, Z., Yin, F., Yuan, Z. (2004). New data on the trade and captive breeding of turtles in Guangxi Province, South China. Asiatic Herpetological Research 10: 126-128 Shi, H., Parham, J.F., Simison, W.B., Wang, J., Gong, S., Fu, B. (2005): A report on the hybridization between two species of

80 Richard P.J.H. Struijk & Torsten E.G. Blanck threatened Asian box turtles (Testudines: Cuora) in the wild on Hainan Island (China) with comments on the origin of serrata - like turtles. Amphibia-Reptilia 26: 377-381. Shi, H., Parham, J., Fan, Z., Hong, M., Yin, F. (2008). Short Communication. Evidence for the massive scale of turtle farming in China. Oryx 42(1): 147-150 Struijk, R.P.J.H., Blanck, T. (2015). Cuora mouhotii mouhotii (Northern Keeled Box Turtle) and C. bourreti (Bourret s Box Turtle). CAPTIVE HYBRIDIZATION. Herpetological Review 46(2): 206. Struijk, R.P.J.H., McCormack, T.E.M., Nguyen, T.T., Pham, T.V., Stumpel, J.B.G. & Auer, M. (in prep.): A case of captive intergradation between Cuora mouhotii mouhotii and Cuora mouhotii obsti and notes on the species distribution range. Stuart, B.L., Parham, J.F. (2004): Molecular phylogeny of the critically endangered Indochinese box turtle (Cuora galbinifrons). Molecular Phylogenetics and Evolution. 31: 164-177. Zhou, T., C. Huang, W.P. McCord, Blanck, T. (2008). Captive Breeding of Hard-Shelled Chelonians in China. Reptilia 61: 27-34 Accepted by Paul Oliver