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Existing Status and Resurgence Strategies for Chinese Alligator (Alligator sinensis)

PJZ_51_3_1169-1177

 

 

Existing Status and Resurgence Strategies for Chinese Alligator (Alligator sinensis)

Iram Maqsood 1,2,3 and Ke Rong *1,2

1College of Wildlife Resources, Northeast Forestry University, Hexing Road 59 Street, Xiang Fang District, Harbin City 150040, China

2Key Laboratory of Conservation Biology, National Forestry and Grassland Administration, Harbin 150040, China

3Department of Zoology, Shaheed Benazir Bhuto Women University, Peshawar, 25000

ABSTRACT

Recently merely two crocodile’s species has been enjoying this universe, and one of them is Chinese alligator (Alligator sinensis) who is at the edge of extinction in nature. Approximately, 130-150 individuals left in wild. Habitat loss is considered as a major source of population decline of this precious species. Consequently, for the sake of A. sinensis conservation, China took steps with the top priority of habitat restoration, controlled management in captive breeding centers, as well as initiation of reintroduction into the wild. Captive breeding centers focused on livestock, controlled sex ratio, promoting growth characteristics, population genetics, and organ preservation. In addition to this, the habitat restoration program committed to improving the quality and habitat area. The reintroduction project illustrated that A. Sinensis bred in captivity well adapted to wild habitat and successfully reproducing their offspring’s. Only healthy crocodiles were selected for release into the wild to renew natural populations. Chinese alligator currently under strict regulation over its commercial use and illegal hunting. All of these strategies give a revival hope to this world most endangered species and give a chance to be part of this ecosystem biodiversity in perspective future. China contributed greatly to conserve ecological and cultural roles of Chinese alligators and its sustainable utilization.


Article Information

Received 25 April 2017

Revised 12 July 2018

Accepted 15 August 2018

Available online 04 April 2019

Authors’ Contribution

IM presented the idea of the research. KR and IM wrote the article. KR provided project for subsidizing the study.

Key words

Chinese alligators, Endangered species, Conservation, Reintroduction program, Captive breeding centers.

DOI: http://dx.doi.org/10.17582/journal.pjz/2019.51.3.rev2

* Corresponding author: [email protected]

0030-9923/2019/0003-1169 $ 9.00/0

Copyright 2019 Zoological Society of Pakistan



Introduction

The International Union for the Conservation of Nature predicted the wild Chinese alligator as being the most endangered among 23 crocodilian species and The Convention was held in international trade of world endangered species and regarded Chinese alligator as Accessory I endangered species (Chen et al., 2003). These alligators are presently prevalent to the lower Yangtze River in China and choose freshwater habitats such as streams, marshes, ponds, lakes, and rice paddies. Previously, during field investigation, some wild nests with less ability to produce viable progeny have been observed. Historically, these species have been dispersed throughout the extensive wetland habitats of the lower Yangtze River (Chen et al.,2003; Thorbjarnarson, 2002). It has estimated that wild habitat carried fewer than 200 individuals and more than 13,000 individuals under captive center management in Anhui and Zhejiang Provinces and that it is decreasing at 4%–6% annually. This severe population bottleneck has been verified by scanning genome-wide single nucleotide polymorphisms (Wan et al., 2013). According to Wildlife Conservation Society, a survey in Shanghai Wetland Park disclosed eggs of Chinese alligators were spotted in a nest and hatching has confirmed by baby alligators founded later (Scott, 2016). To raise the number of wild alligators, since 2003 the reserve has reintroduced a bunch of the reptiles to their natural habitat. After the uninterrupted four months of dormancy period, over 13,000 Yangtze alligators have spotted outside to make them enjoy the warm sunshine of spring in Xuancheng, East China’s Anhui province, in order (Xinhua, 2017).

Until now Chinese alligators population affected by varied factors but mostly included habitat fragmentation and degradation, shooting, natural disasters, geographic separation, low productivity, and pollution. The supreme priority for the conservation of A. sinensis is habitat reestablishment to achieve the goal of the reintroduction of captive bred individuals. Additionally, the potential aftermath of environmental pollution and reduced genetic diversity of the wild population must be addressed (Ding et al., 2004). The SFA broadcasted the “China Action Plan for Conservation and Introduction of Chinese Alligator” in 2002 and catalog A. sinensis as one of 15 leading species of National Wildlife Conservation Project (Jiang, 2010). Since then, the Chinese Government has paid more attention to the protection and management of wild populations and their habitats, as well as speed up release projects. The reintroduction program initiated in 2001 by ANNRCA (Jiang et al., 2006).

Although conservation efforts for this species in China began in 1979, efforts have focused on the wild population only since 2000. Some of the following conservation strategies are under consideration until now.

 

Establishment of Captive breeding centers

Chinese alligator conservationist has focused on captive breeding and established centers in Anhui and Zhejiang Provinces (Wan et al., 1998). The Anhui Research Center for Chinese Alligator Reproduction (ARCCAR) is the biggest facility, housing over 13,000 A. sinensis and assisting as the administrative center for alligator conservation in Anhui Province, controlling 5-county and 13 protected sites that covered all the remaining regions with wild Chinese alligators. In spite of this, breeding centers have been set up at Qiongshan City, National Forest Park of Qiandaohu, Doumen County, and Jiangyin City. Additionally, numerous small-scale safari parks, museums, and captive-breeding farms also maintain A. sinensis (e.g., Chongqing and Shanghai Municipalities). Chinese alligators breeding has also been practicing in the United States at the Bronx Zoo (New York), St. Augustine Alligator Farm (Florida), and Rockefeller Refuge (Louisiana). Specimens are seized in zoos and private holdings outside of China, and the index is well-maintained for the USA and Europe (Jensch, 2008). Guangzhou motive has issued at the International Workshop on Captive Breeding and Commerce Management in Crocodylia in order to support captive breeding and commerce running of crocodilians in China (SFA, 2002). To provide good living condition and ease the stress of the large captive population, State Forestry Administration (SFA) of China and Anhui Provincial Government co-financed ARCCAR to construct well-facilitated breeding areas. Meanwhile, in 2003 the SFA and Changxing Government co-financed for CBRCCA to facilitate infrastructure and wetland restoration (Jiang, 2010). Captive breeding centers have focused on many aspects of Chinese alligators, which are as follows:

Sexual development of Chinese alligator

In addition to population survival and development, the sex ratio is a major issue of mate competition and mate selection among all species (Oring and Emlen, 1977; Hurst and Dyson, 2004). Preference towards one sex in a small isolated population influence the extinction of a species. Therefore, the appropriate sex ratio for Chinese alligator should maintain in order to recover wild populations. Numerous studies reported that inbreeding depression is a major problem for population recovery as it disturbed natural male-to-female sex ratio of Chinese alligator (Wang and Ding, 2004; Zhang et al., 2006; Wang et al.,2006). For several decades, the Chinese alligator has been subject to population bottlenecks. Genome-wide single nucleotide polymorphism advocated major inbreeding within populations (Wan et al., 2013). To maximize the number of offspring under inbreeding pressure, more females produce than males (Hamilton, 1967), which could lessen the effect of low survival rates on overall population development. The female-biased sex ratio for regardless of mate-competition requires a polygynous mating system to achieve an efficient reproduction (Lance et al., 2009). To overcome sex ratio, the improvements have been achieved in sex development of Chinese alligator by using a reptile scale incubator under automatic temperature and humidity recorders with highest survival rate. Incubation at 29 degrees produces female with 91.67% survival rate and Incubation at 34 degrees produces male with 87.50% survival rate (Fang and Fang, 2015).

Investigation of hormonal development

In recent years, reproductive biology got consideration by the various researcher to examine the mechanism of reproductive hormones. Zhang et al. (2015) have investigated the changes in expression of FSHß during the reproductive cycle. He explored the mechanisms that regulate the reproduction of the Chinese alligator and it might play an important role in promoting ovarian development. It might be a contribution towards producing Recombinant Chinese alligator FSHß, which could assist in artificial breeding aimed to increase its captive reproductive efficiency. Another fact-finding revealed that ESR1 mRNA plays an important role in the mediation of estrogenic multiple reproductive effects in Chinese alligator because the highest level has recorded in the ovary as compared to other organs (Zhang et al., 2016). Consideration toward growth development also plays a key contribution in Chinese alligator management.

Explore development factors

The insulin-like growth factors (IGFs) play an essential role in growth and development (Moriyama et al., 2000; Ohlsson et al., 2009). It has already been established that IGF-I is predominately produced in the liver and release into the circulation (Hu et al., 2006; Ponce et al., 2008; Escobar et al., 2011; Zhang et al., 2013). Investigation illustrated that Chinese alligator IGF-I (caI GF-I) have a supreme role in the regulation of growth and development during the active and hibernating periods. Recombinant caI GF-I might be tested to increase the captive growth rate of the Chinese alligator (Xue et al., 2017). An investigation conducted during early postnatal growth in Alligator sinensis, proposed that Nerve growth factor (NGF) expression is involved in several structures of the partial central nervous system (Zheng et al., 2013). Zhang et al. (2015) advocated that B-cell activating factor (BAFF) has involved in survival and proliferation of B cells of Alligator sinensis. Further, the phylogenetic investigation revealed that Alligator sinensis BAFF gene is a sister group of birds and reptiles that indicate that they have evolved from a common ancestor.

Genetic resolution

Genetic status of captive populations and the remaining wild individuals has not been well described due to scarcity in the information of genetic markers, impeding the efforts of organizing a well-structured reintroduction strategy. Microsatellite markers could be advantageous in selecting of proper individuals for reintroduction plan, might advocate some important conservation queries. Xu et al. (2006) found 8 polymorphic loci in Chinese alligator with 26 alleles among 32 animals yielding an average of 3.25 alleles per polymorphic locus. He has illustrated that joint polymorphic loci could be sensitive markers in genetic diversity investigation and analogous inference within the Chinese alligator populations. Microsatellites as a class of highly variable genetic markers are widely distributed in eukaryotic genomes and have been used in numerous crocodilian population studies. Ten more polymorphic microsatellite loci were isolated from the Chinese alligator (Alligator sinensis). These unique molecular markers were suitable for population genetic studies and kinship investigation within A. sinensis population (Zhu et al., 2009). Furthermore, these ten microsatellite loci were tested for the selection of Individuals with maximum genetic differences from captive-bred Chinese alligators. It is very crucial to use an appropriate molecular marker to inspect the genetic diversity before reintroduction of an unrelated alligator into a particular wild area (Zhu et al., 2010). An important part of the Chinese alligator conservation project is the preservation of organs, tissues, sperm, oocytes, embryos and genomic DNA libraries. Furthermore, somatic cells have become an attractive resource for conserving rare and endangered species genetic materials with the flourish of Cytogenetic methods and induced pluripotent stem cell techniques. Researcher established three cell lines from liver, heart and muscle tissues of the Chinese alligator and preserved at –196°C, this contribution is a vital asset for the protection of this rare and critically endangered species (Zeng et al., 2011).

 

Wetland stability

There is a persistent need to solve many problems related to wetland conservation and biodiversity conservation in China (Wang et al., 2017). The first priority concern with the severe decrease in the area of wetlands. The estimated area was 660,000 km2 in 2005 (Liu and Diamond, 2005) but in 2009 it has reported that it decreased to 359,478 km2 (Niu et al., 2009), causing a sharp habitat destruction for numerous species. For instance, the Yangzi reserve and Freshwater National Nature Reserve play a principal role in the protection of Chinese alligator. Most of the central and southern China reserves with the maximum protection value were located in in the middle and lower reaches of the Yangtze River. The wetland ecosystems in these reserves are in the form of lakes, rivers, and marshes and representative for the diversity of threatened and endemic species. In southern Anhui Province, alligators are limited to a small number of agricultural ponds within a five-county region (Wan et al., 1998; Thorbjarnarson and Wang, 1999). Breeding centers, zoos in China and North America carry a reasonably large number of captive population (Behler, 1995; Wan et al., 1998). Various organizations involved in the restoration of wetlands or investigation of existing areas with a suitable living condition where captive-reared alligators can be released (Wan et al., 1998; Thorbjarnarson and Wang, 1999). In 2003, The UNDP-GEF Support the Effectiveness of the Protected Area System in Anhui Province, this project assist in Anhui Wetland project to restore habitat for the Yangtze alligators and other species. All these efforts contribute to management effectiveness of the Wetland Protected Area (WPA) systems in Anhui and emerging threats to the globally significant biodiversity and essential ecosystem. Wang et al. (2011) suggested that southern part of the pond might play a crucial role by creating buffer areas between farmland and the edge of the pond. The buffer areas should be covered with vegetation to ensure that the alligators bask out of the water and can conceal themselves from farming activities.

 

Reintroduction of Chinese Alligator

International Workshop on Conservation and Reintroduction of Chinese Alligator was held in 2001 (SFA, 2002). The Anhui Yangtze Alligator NNR initiate its first step toward the captive-release program in 2002. In 2003, one of the protected sites Hong Xing Reservoir welcomed three captive-reared alligators. Another reintroduction site, Gaojingmiao Forest Farm (GFF), was evaluated as a reintroduction sit. The SFA has approved a Construction plan for Chinese alligators release in Zhejiang Province in October 2006 and introduced with 6, 6 and 9 alligators in 2006, 2007 and 2008 respectively. In 2008, one A. sinensis nest constituting 17 out of 19 fertile eggs were discovered at GFF by ANNRCA staff (Jiang, 2008). Further Chinese alligators from U.S. zoos have introduced to breeding centers in China to treasured genetic diversity in captive populations. Later in 2015, 6 more alligators from Anhui Chinese Alligator National Nature Reserve were transferred into Dongtan Wetland Park (www.sciencedaily.com/releases/2016/10/161026133227.htm). The second batch of 12 captive-bred Chinese alligators from Anhui National Nature Reserve for Chinese Alligators was released into the wild in Xuancheng (SFA, 2015). So far, the NNR has released approximately 100 alligators into the wild. All of these efforts indicated that captive-reared A. sinensis well adapted to restored habitats and retained breeding capacity in the wild. These statements signal a huge success for the species and for ongoing reintroduction efforts initiated by the different organization of china.

Nesting ecology

Previous studies about nesting ecology of A. Sinensis illustrated that nesting and egg-laying time were affected by the weather condition and moisture in the area (Jiang and Xia, 2005). Distance to water and thickness of vegetation canopy also affected the selection of nesting sites (Zhang et al., 2006). Sites with 63% to 88% vegetation coverage have observed more suitable for A. sinensis nesting (Zhou, 2007). The study has conducted in reintroduction locality for A. sinensis similar to natural habitat. Vegetation coverage was measured as a most important variable affecting the nesting of the Chinese alligator (Zhang et al., 2003; Jiang and Xia, 2005). Previously sunlight duration was not measured; however, sunlight duration has the greatest scores in PC1. Consequently, it has also considered as a principal variable affecting the nest-site choice in a natural habitat because the sunshine is a source for nest temperature (Magnusson and Lima, 1985; Chen and Li, 1979). Too high nest temperature lead to hatching failure and too little sunlight resulted in low temperature for successful incubation. Therefore, Chinese alligators preferred habitat with the correct level of sunlight duration for nesting. Additionally, nest temperature in a certain range is also proportional to incubation time (Zhou and Wang, 2000). Nesting ecology is an important judgment for the Chinese alligator reintroduction. It has estimated that a reintroduction area with sunlight duration of 5 h and nearest bank slope of 46° was more suitable for the Chinese alligators nesting (Jianjun et al., 2011).

Witnessing animal health

Before releasing captive animals, it is very important to examine the health of captive breed animals (Plowright, 1988; May, 1991; Kock and Woodford, 1991; Mills, 1999). Previously, bacteriological methods and molecular biology methods have used to identify bacterial genera revealed that captive alligator was a source of introducing pathogenic bacteria into the wild environment and could be endangering the native wild populations. It was strongly advised that the bacteria from the cloaca of Chinese alligators should be checked before release and reintroduction into the wild in order to avoid potential ecological harm (Ma et al., 2008). Consequently, only healthy captive-bred alligators were selected and release into the wild to renew the natural populations. Additionally, PHCs are endocrine-disrupting compounds, which can be maternally transferred to developing alligator eggs, is a major source for reduced hatchling success, promote embryonic mortality (Guillette et al., 2000; Rauschenberger et al., 2004a; b; 2007; Stoker et al., 2011). Evidence has provided for PHC presence in captive Chinese alligators and has investigated that these chemicals can be maternally transferred to the eggs. Thus, it is important to monitor the concentrations of PHCs in Chinese alligators before reintroduction into the wild. This investigation cooperates in alligator conservation plan because reptile species in the early stages of life are very sensitive to these chemicals. He found that DDTs were the most dominant among the investigated PHCs in Chinese alligators with mean contributions of >90%. Eggs examination of captive Chinese alligators revealed exceeded levels of DDTs and PCBs l caused impair reptile reproduction (Ting et al., 2014).

 

Environmental pollution investigation

China is facing increasing problems with a variety of environmental contaminants including PFASs (Bao et al., 2010). Captive animals near urban industrialized areas have experienced contaminants, adversely affecting their health. Currently assessed PFASs exposure in Chinese alligators from a conservation center situated in an urbanized region of China. Further, gender and age-specific PFASs accumulation were investigated and discovered the sources of PFAS contamination. PFAS pollution is common in eastern China and prevalent the lower reaches of the Yangtze River (So et al., 2007; Yeung et al., 2008). Exposure to these chemicals has been investigated by Serum examination of Chinese alligators, which revealed various levels of PFASs. It was also observed that level of PFTeDA, PFDoDA, PFUnDA, PFDA, and PFNA decreased with the increase in age (Jianshe et al., 2013).


 

Population monitoring and catalog

Breeding centers have been proven successful in the management of captive Chinese alligators and the carried more than 10,000 individuals at the Anhui Research Center for Chinese Alligator Reproduction (ARCCAR) (Thorbjarnarson, 2002; Chen et al., 2003). Even though successful achievement in a captive population of the ANNRCA, the wild population has continued to decline with the estimation of <25% of the 1980s. Recorded data in 2002 indicated that total wild population had declined from approximately 1000 alligators in the late 1970s to ≥130 (Thorbjarnarson, 2002). Further observations in 2004 revealed a continuous decline in wild population with the total number of fewer than 120 individuals in China (Ding et al., 2004). In 2005, investigations indicated a slight drop in an approximate number of 92-114 wild individuals (Jiang et al., 2006; Wu et al., 2008), and most sites were found with the stable wild population. Further monitoring indicated successful breeding in 2004 and 2005 results in increasing population in Hong Xing, Zhucun, Zhuangtou and Heyi (Jiang et al., 2006). By 2007, entire stocks exceeded 630 alligators, with 100-200 hatchlings produced annually (Wu et al., 2008). To find out their activity area and movement pattern different methods like Radio telemetry, direct observation by binoculars in daytime and spotlight night counting in nighttime has used. Observation illustrated that activity varied per individual but the male has a relative larger activity area than females. It has observed that sometimes, captive release alligators showed conflict with native ones and prefer bank edge with vegetation coverage to live (Ding et al., 2003). It has documented in 2013 that there were ~100 wild Chinese alligators and ~10,000 captive individuals in Anhui and Zhejiang Provinces (Wan et al., 2013).

Wildlife Conservation Society disclosed that eggs of Chinese alligators spotted recently in a nest of Shanghai Wetland Park have hatched and that baby alligators have been detected (Scott, 2016). Currently, It has estimated that there are more than 13,000 alligators in captive and approximately 130 to 150 individual in wild (Fig. 1) (Xinhua, 2017).

 

Impede Illegal Hunting and Commerce for Chinese Alligators

As one of the highly endangered crocodilians in the world, Chinese alligators have been secured with the maximum effort of Chinese and international law over the past years (Wan et al., 1998). The captive-bred population in Anhui Research Center for Chinese Alligator Reproduction (ARCCAR) has successfully raised over 13,000 alligators under the breeding program (Xinhua, 2017). By 1992 export of second filial (F2) generation of alligators have been legalized by CITES, further commercial development and application of Chinese alligators have allowed in China. Previously, permitted commercial meat from farmed Chinese alligators have appeared in the market (Wu and Chen, 1999). However, State Forestry Administration of China (SFA) only authorized four restaurants in whole china to trade meat of Chinese alligators. Identification by morphological characteristics does not work because of Resemblances between the Chinese alligator meat and other animal meat. Molecular technology by polymerase chain reaction (PCR) provides a power tool to identify Chinese alligator meat, as well as prevent illegal trade of Chinese alligators and the hunting of some of this critical endangered wild animal (McVeigh et al., 1991; Meyer et al.,1995; Koh et al., 1998; Sanjuan and Comesana, 2002; Abdulmawjood and Buelte, 2002; Chang et al., 2003; Rodriguez et al., 2003). Additionally, single one PCR step with species-specific PCR primers has been used to identify the Chinese alligator meat by the multiplex PCR. This method has proved very powerful in identification of meat and other goods from Chinese alligators (Rodriguez et al., 2003).

 

Conclusions

Despite the world, most endangered species, researcher have gained successful achievements in managing this precious species. Pollution control should be the first priority followed the habitat reestablishment and reintroduction of captive bred individuals. Although great success has been acquired in captive and wild alligator population since there is a need to pay more attention toward the protection and management of wild populations, as well as release projects. Captive-bred centers are struggling hard in order to achieve genetic diversity by releasing genetically unrelated individual into wild. Moreover, as it is well known that researchers can control sex development of Chinese alligator in controlled conditions but still there is a need to develop more tactics to control sex development in wild. The goals of Conservation and Reintroduction of Chinese Alligator project, Anhui Wetland project and Preservation Project for Chinese alligator ‘organs, tissues, sperm, oocytes, embryos and genomic DNA libraries are huge hope for Chinese alligator survival on this planet.

 

Acknowledgment

This work was supported by the National natural science Fund of China (31372209).

 

Statement of conflict of interest

Authors declare that there is no conflict of interest.

 

References

Abdulmawjood, A. and Buelte, M., 2002. Identification of Ostrich meat by restriction fragment length polymorphism (RFLP) analysis of cytochrome b gene. J. Fd. Sci., 5: 1688–1691. https://doi.org/10.1111/j.1365-2621.2002.tb08706.x

Bao, J., Liu, W., Liu, L., Jin, Y., Ran, X. and Zhang, Z., 2010. Perfluorinated compounds in urban river sediments from Guangzhou and Shanghai of China. Chemosphere, 80: 123–130. https://doi.org/10.1016/j.chemosphere.2010.04.008

Behler, J., 1995. AZA annual report on conservation and science. In: Chinese alligator (Alligators sinensis). American Zoo and Aquarium Association, Bethesda, MD, pp. 255–256.

Chang, K.C., Beuzena, N.D. and Hallb, A.D., 2003. Identification of microsatellites in expressed muscle genes: assessment of a desmin (CT) dinucleotide repeat as a marker for meat quality. Vet. J., 165: 157–163. https://doi.org/10.1016/S1090-0233(02)00159-4

Chen, B.H. and Li, B.H., 1979. Primary studies on the ecology of Chinese alligator. J. Anhui Normal Univ. (Nat. Sci.), 1: 69–78.

Chen, B.H., Hua, T.M., Wu, X.B. and Wang, C.L., 2003. Research on the Chinese alligator. Education Press of Sciences and Technology, Shanghai, pp. 249–250 (In Chinese).

Ding, Y.Z., Wang, X.M., Wang, Z.H., Wu, J.S. and John, T., 2003. Observation of activity in Chinese alligators released during an early period at Hongxing of Anhui. Zool. Res., 25: 27–31.

Ding, Y., Wang, X., Thorbjarnarson, J., Wu, J., Wang, Z., Wu, W., Gu, C. and N.J., 2004. Movement patterns of released captive-reared Chinese alligators (Alligator sinensis). In: Proceedings of the 17th Working Meeting of the IUCN-SSC Crocodile Specialist Group. Gland, IUCN, pp. 109.

Escobar, S., Fuentes, E.N., Poblete, E., Valdés, J.A., Safian, D., Reyes, A.E., Alvarez, M. and Molina, A., 2011. Molecular cloning of IGF-I and IGF-I receptor and their expression pattern in the Chilean flounder (Paralichthys adspersus). Comp. Biochem. Physiol. B: Biochem. mol. Biol., 159: 140–147. https://doi.org/10.1016/j.cbpb.2011.03.003

Fang, S. and Fang, L., 2015. The fully automatic egg incubator directs the sexual development of Chinese alligator. Chinese J. Wildl., 36: 103–107.

Guillette, J., Crain, D.A., Gunderson, M.P., Kools, S.A.E., Milnes, M.R., Orlando, E.F., Rooney, A.A. and Woodward, A.R., 2000. Alligators and endocrine disrupting contaminants: A current perspective. Am. Zool., 40: 438–452. https://doi.org/10.1093/icb/40.3.438

Hamilton, W.D., 1967. Extraordinary sex ratios. Science, 156: 477–488. https://doi.org/10.1126/science.156.3774.477

Hu, X.L., Zhu, M.Y., Zhang, Z.H., Hou, R., Shen, F.J., Li, F.Z. and Zhang, A.J., 2006. Cloning, characterization and tissue specific expression of Amur Tiger (Panthera tigris altaica) IGF-I. Biosci. Biotechnol. Biochem., 70: 1846–1854. https://doi.org/10.1271/bbb.60008

Hurst, G.D. and Dyson, E.A., 2004. Persistence of an extreme sex-ratio bias in a natural population. Proc. Natl. Acad. Sci., 101: 6520–6523. https://doi.org/10.1073/pnas.0304068101

Jensch, B., 2008. DGHT studbook for Chinese Alligator. Croco. Special. Group Newsl., 27: 12.

Jiang, H.X., 2010. Chinese alligator Alligator sinensis. In: Crocodiles - Status survey and conservation action plan (eds. S.C. Manolis and C. Stevenson). Crocodile Specialist Group, Darwin, pp. 5-9.

Jiang, H.X., 2008. Reintroduction achievement for Chinese alligator. Croco. Special. Group Newsl., 27: 9–10.

Jiang, H.X., Chu, G.Z., Ruan, X.D., Wu, X.B., Shi, K. and Wang, Z., 2006. Implementation of China action plan for conservation and reintroduction of Chinese alligator. In: Proceedings of the 18th Working Meeting of the IUCN-SSC Crocodile Specialist Group. Gland, IUCN, pp. 322–332.

Jiang, X.Q. and Xia, T.S., 2005. Effect of environmental factors on nesting and laying eggs of Chinese alligator in captivity. Sichuan J. Zool., 24: 373–377.

Jianjun, W., Xiaobing, W.U., Dawei, T., Jialong, Z. Renping, W. and Chaolin, W., 2011. Nest-site use by the Chinese alligator (Alligator sinensis) in the Gaojingmiao Breeding Farm, Anhui, China. Asiat. Herpetol. Res., 2: 36–40. https://doi.org/10.3724/SP.J.1245.2011.00036

Jianshe, W., Yating, Z., Fang, Z., Leo, W.Y.Y. , Sachi, T., Eriko, Y., Renping, W., Paul, K.S.L. and Nobuyoshi, Y., 2013. Age- and gender-related accumulation of perfluoroalkyl substances in captive Chinese alligators (Alligator sinensis). Environ. Pollut., 179: 61–67. https://doi.org/10.1016/j.envpol.2013.04.020

Kock, R.A. and Woodford, H.M., 1991. Veterinary considerations in reintroduction and translocation projects. In: Beyond captive breeding: Re-introducing endangered (ed. J.H.W. Gipps). Clarendon Press, Oxford, pp. 101-110.

Koh, M.C., Lim, C.H., Chua, S.B., Chew, S.T. and Phang, S.T.W., 1998. Random amplified polymorphic PCR (RAPD) fingerprints for identification of red meat animal’s species. Meat Sci., 48: 275–285. https://doi.org/10.1016/S0309-1740(97)00104-6

Lance, S.L., Tuberville, T.D., Dueck, L., Holz-Schietinger, C., Trosclair, P.L., Elsey, R.M. and Glenn, T.C., 2009. Multiyear multiple paternity and mate fidelity in the American alligator Alligator mississippiensis. Mol. Ecol., 18: 4508–4520. https://doi.org/10.1111/j.1365-294X.2009.04373.x

Liu, J. and Diamond, J., 2005. China’s environment in a globalizing world. Nature, 435: 1179–1186. https://doi.org/10.1038/4351179a

Ma, R.R., Wu, X.B., Jiang, H. X., Pan, J.H. and Zhu, J.L., 2008. Identification of cloaca bacteria from candidate releasing Chinese alligators. Zool. Res., 29: 253–259. https://doi.org/10.3724/SP.J.1141.2008.00253

Magnusson, W.E. and Lima, A.P., 1985. Sources of heat for nests of Paleosuchus trigonatus and a review of crocodilian nest temperatures. J. Herpetol., 19: 199–207. https://doi.org/10.2307/1564173

May, R.M., 1991. The role of ecological theory in planning reintroduction. In: Symposia of the Zoological Society of London. Clarendon Press, Oxford, pp. 145-163.

McVeigh, H.P., Bartlett, S.E. and Davidson, W.S., 1991. Polymerase chain reaction/direct sequence analysis of the cytochrome b gene in Salmo salar. Aquaculture, 95: 225–223. https://doi.org/10.1016/0044-8486(91)90089-P

Meyer, R., Hofelein, C., Luthy, J. and Candrian, U., 1995. Polymerase chain reaction–restriction fragment length polymorphism analysis: A simple method for species identification in food. J. Assoc. Official Analyt. Chemists Int., 78: 1542–1551.

Mills, C., 1999. The wild, wild pest. The Sciences, 3: 10–13. https://doi.org/10.1002/j.2326-1951.1999.tb03420.x

Moriyama, S., Ayson, F.G. and Kawauchi, H., 2000. Growth regulation by insulin-like growth factor-I in fish. Biosci. Biotechnol. Biochem., 64: 1553–1562. https://doi.org/10.1271/bbb.64.1553

Niu, Z.G., Gong, P., Cheng, X., Guo, J.H., Wang, L., Huang, H.B., Shen, S.Q., Wu, Y.Z., Wang, X.F., Wang, X.W., Ying, Q., Liang, L., Zhang, L.N., Wang, L., Yao, Q., Yang, Z.Z., Guo, Z.Q. and Dai, Y.J., 2009. Remote sensing of wetland mapping and initial analysis of the relevant geographical features. Sci. China Ser. D: Earth Sci., 39: 188–203.

Ohlsson, C., Mohan, S., Sjögren, K., Tivesten, A., Isgaard, J., Isaksson, O., Jansson, J.O. and Svensson, J., 2009. The role of liver-derived insulin-like growth factor-I. Endocr. Rev., 30: 494–535. https://doi.org/10.1210/er.2009-0010

Oring, L.W. and Emlen, S.T., 1977. Ecology, sexual selection, and the evolution of mating systems. Science, 197: 215–223. https://doi.org/10.1126/science.327542

Plowright, W., 1988. Viruses transmissible between wild and domestic animals. In: Symposia of the Zoological Society of London (eds. G.R. Smith and J.P. Hearn). Clarendon Press, Oxford, London, pp. 60.

Ponce, M., Infante, C., Funes, V. and Manchado, M., 2008. Molecular characterization and gene expression analysis of insulin-like growth factors I and II in the red banded seabream, Pagrus auriga: Transcriptional regulation by growth hormone. Comp. Biochem. Physiol. B: Biochem. mol. Biol., 150: 418–426. https://doi.org/10.1016/j.cbpb.2008.04.013

Rauschenberger, R.H., Sepúlveda, M.S., Wiebe, J.J., Szabo, N.J. and Gross, T.S., 2004. Predicting maternal body burdens of organochlorine pesticides from eggs and evidence of maternal transfer in Alligator mississippiensis. Environ. Toxicol. Chem., 23: 2906–2915. https://doi.org/10.1897/03-584.1

Rauschenberger, R.H., Wiebe, J.J., Buckland, J.E., Smith, J.T., Sepúlveda, M.S. and Gross, T.S., 2004. Achieving environmentally relevant organochlorine pesticide concentrations in eggs through maternal exposure in Alligator mississippiensis. Mar. environ. Res., 58: 851–856. https://doi.org/10.1016/j.marenvres.2004.03.104

Rauschenberger, R.H., Wiebe, J.J., Sepúlveda, M.S., Scarborough, J. and Gross, T.S., 2007. Parental exposure to pesticides and poor clutch viability in American alligators. Environ. Sci. Technol., 41: 5559–5563. https://doi.org/10.1021/es0628194

Rodriguez, M.A., Garcia, T., Gonzalez, I., Asensio, L., Mayoral, B., Lopez-Calleja, I., Hernandez, P.E. and Martin, R., 2003. Identification of goose, male duck, chicken, turkey, and swine in fore gars by species-specific polymerase chain reaction. J. Agric. Fd. Chem., 51: 1524–1529. https://doi.org/10.1021/jf025784+

Rui, Z., Shengzhou, Z., Xue, Z. and Yongkang, Z., 2015. Molecular characterization of the Chinese alligator follicle-stimulating hormone ß subunit (FSHß) and its expression during the female reproductive cycle. Comp. Biochem. Physiol., 2: 49–57.

Sanjuan, A. and Comesana, A.S., 2002. Molecular identification of nine commercial flatfish species by polymerase chain reaction–restriction fragment length polymorphism analysis of a segment of the cytochrome b region. J. Fd. Protect., 65:1016–1023. https://doi.org/10.4315/0362-028X-65.6.1016

Scott, S., 2016. World’s most endangered alligator making a comeback in Shanghai. Wildlife Conservation Society. Available at: https://newsroom.wcs.org/News-Releases/articleType/ArticleView/articleId/9363/Worlds-Most-Endangered-Alligator-Making-a-Comeback-in-Shanghai.aspx (Accessed 3 march 2017)

SFA, 2015. China released endangered alligators into wild. Chinese Academy of Forestry. Available at: http://english.forestry.gov.cn/index.php/forestry-science-education/727-china-released-endangered-alligators-into-wild (Accessed January 1, 2017).

SFA, 2002. Status quo and future of conservation for Chinese alligator and crocodiles in the world. Proceedings of International Workshop on Conservation and Reintroduction of Chinese Alligator, 25-28 August 2001, Hefei City, Anhui Province, China.

So, M.K., Miyake, Y., Yeung, W.Y., Ho, Y.M., Taniyasu, S., Rostkowski, P., Yamashita, N., Zhou, B.S., Shi, X.J., Wang, J.X., Giesy, J.P., Yu, H. and Lam, P.K., 2007. Perfluorinated compounds in the Pearl River and Yangtze River of China. Chemosphere, 68: 2085–2095. https://doi.org/10.1016/j.chemosphere.2007.02.008

Stoker, C., Repetti, M.R., García, S.R., Zayas, M.A., Galoppo, G.H., Beldoménico, H.R., Luque, E.H. and Muñoz-de-Toro, M., 2011. Organochlorine compound residues in the eggs of broad-snouted caimans (Caiman latirostris) and correlation with measures of reproductive performance. Chemosphere, 84: 311–317. https://doi.org/10.1016/j.chemosphere.2011.04.013

Thorbjarnarson, J., 2002. Wild Populations of the Chinese alligator approach extinction. Biol. Conserv., 103: 93–102. https://doi.org/10.1016/S0006-3207(01)00128-8

Thorbjarnarson, J. and Wang, X., 1999. The conservation status of the Chinese alligator. Oryx, 33: 152–159. https://doi.org/10.1046/j.1365-3008.1999.00051.x

Ting, W., Bing, H., Xiaobing, W, Jiangping, W., Xinming, W., Zhigang, Y., Juan, Z. and Miao, Z., 2014. Persistent halogenated compounds in captive Chinese alligators (Alligator sinensis) from China. Chemosphere, 110: 23–30. https://doi.org/10.1016/j.chemosphere.2014.03.015

Wan, Q.H., Pan, S.K., Hu, L., Zhu, Y., Xu, P.W. and Xia, J.Q., 2013. Genome analysis and signature discovery for diving and sensory properties of the endangered Chinese alligator. Cell Res., 23: 1091–1105. https://doi.org/10.1038/cr.2013.104

Wan, Z., Gu, C., Wang, X., 1998. Conservation, management, and farming of crocodiles in China. In: Proceedings of the 14th Working Meeting of the Crocodile Specialist Group. IUCN-The World Conservation Union, Gland, Switzerland, pp. 80–100.

Wang, X.M. and Ding, Y.Z., 2004. Factors influencing the population status of wild Chinese alligator Alligator sinensis. Biodiv. Sci., 12: 324–332.

Wang, X. Y., Wang, D., Wu, X. B., Wang, R.P. and Wang, C.L., 2006. Congregative effect of Chinese alligator’s bellowing chorus in mating season and its function in reproduction. Acta Zool. Sin., 52: 663–668.

Wang, Z., Yao, H., Ding, Y., Thorbjarnarson, J. and Wang, X., 2011. Testing reintroduction as a conservation strategy for the critically endangered Chinese alligator: Movements and home range of released captive individuals. Chin. Sci. Bull., 56: 2586–2593. https://doi.org/10.1007/s11434-011-4615-8

Wang, S., Zhao, Y., Xu, Z., Li, L., Wu, L., Duan, C. and Peng, J., 2017. Behavioural Rhythms during the adaptive phase of introduced milu/père David’s Deer, Elaphurus davidianus, in the Dongting Lake Wetland, China. Pakistan J. Zool., 49: 1657-1664.

Wu, X.B. and Chen, B.H., 1999. The number and value of Alligator sinensis resource and current situation of its exploitation and utilization. J. Nat. Resour., 2:183–187.

Wu, X.B., Gu, C.M., Zhu, J.L., Wang, C.L., Jiang, H.X., Shao, M. and Meng, W.Z., 2008. Integrated Research of Anhui National Nature Reserve for Chinese Alligator. Anhui Industry Publishing House, Hefei (in Chinese).

Xinhua, 2017. Over 13,000 alligators move out of the houses. China daily. Available at: http://www.chinadaily.com.cn/china/2017-03/20/content_28607795.htm (Accessed March 20, 2017).

Xu, Q., Fang, S., Wang, Z. and Wang, Z., 2006. Microsatellite analysis of genetic diversity in the Chinese alligator (Alligator sinensis) Changxing captive population. Conserv. Genet., 6: 941–951. https://doi.org/10.1007/s10592-005-9081-x

Xue, Z., Shengzhou, Z., Shuai, Z., Rui, Z., Yongkang, Z. and Xiaobing, W., 2017. Insulin-like growth factor I (IGF-I) in Chinese alligator, Alligator sinensis: Molecular characterization, tissue distribution, and mRNA expression changes during the active and hibernating periods. Gen. Comp. Endocr., 242: 74–82. https://doi.org/10.1016/j.ygcen.2015.11.003

Yeung, L.W., Miyake, Y., Taniyasu, S., Wang, Y., Yu, H., So, M.K., Jiang, G., Wu, Y., Li, J., Giesy, J.P., Yamashita, N. and Lam, P.K., 2008. Perfluorinated compounds and total and extractable organic fluorine in human blood samples from China. Environ. Sci. Technol., 42: 8140–8145. https://doi.org/10.1021/es800631n

Zeng, C., Ye, Q. and Fang, S., 2011. Establishment and cryopreservation of liver, heart and muscle cell lines derived from the Chinese alligator (Alligator sinensis). Chinese Sci. Bull., 56: 2576–2579. https://doi.org/10.1007/s11434-011-4622-9

Zhang, F., Wu, X., Meng, W. and Zhu, J., 2006. Ecology on the making nest and laying eggs of Chinese alligator Alligator sinensis under artificial feeding conditions. Zool. Res., 27: 151–156.

Zhang, F., Jiang, H. X., Wu, L. S., Wu, X. B. and Xue, H., 2003. Analysis on the survival environment affecting wild Chinese alligator. Sichuan J. Zool., 26: 374–377.

Zhang, F., Wu, X.B. and Meng, W.Z., 2006. Ecology on the making nest and laying eggs of Chinese alligator (Alligator sinensis) under artificial feeding conditions. Zool. Res., 27: 2151-2156.

Zhang, J.X., Song, R., Sang, M., Sun, S. Q., Ma, L., Zhang, J. and Zhang, S.Q., 2015. Molecular and functional characterization of BAFF from the Yangtze alligator (Alligator sinensis, Alligatoridae). Zoology, 118: 325–333. https://doi.org/10.1016/j.zool.2015.03.003

Zhang, J., Yang, R., Sun, S., Sun, L., Liu, Y., Zhang, Y., Yan, S., Li, Y. and Zhao, Z., 2013. Cloning and characterization of new transcript variants of insulin-like growth factor- I in Sika deer (Cervus elaphus). Growth Horm. IGF Res., 23: 120–127. https://doi.org/10.1016/j.ghir.2013.04.003

Zhang, R., Hu, Y., Wang, H., Yan, P., Yongkang. Z., Rong, W. and Xiaobing, W., 2016. Molecular cloning, characterization, tissue distribution and mRNA expression changes during the hibernation and reproductive periods of estrogen receptor alpha (ESR1) in Chinese alligator, Alligator sinensis. Biochem. mol. Biol., 200: 28–35. https://doi.org/10.1016/j.cbpb.2016.05.001

Zheng, L., Chen, F., Wang, R., Zhou, Y. and Wu, X., 2013. Temporal profile of nerve growth factor expression in the partial central nervous system of the Yangtze alligator Alligator sinensis (Reptilia: Crocodylia ) during early postnatal growth. Anat. Rec., 296: 840–845. https://doi.org/10.1002/ar.22682

Zhou, K.H., 2007. Influence of cover degree of vegetation on selecting nest and incubating egg of Chinese alligator. Sichuan J. Zool., 26: 422–424.

Zhou, Y.K. and Wang, R.P., 2000. Influence of incubation temperature on development and yolk retention in hatchlings of Alligator sinensis. Sichuan J. Zool., 19: 167–169.

Zhu, H., Wu, X., Xue, H., Wei, L. and Hu, Y., 2009. Isolation of polymorphic microsatellite loci from the Chinese alligator (Alligator sinensis). Mol. Ecol. Resour., 9: 892–894. https://doi.org/10.1111/j.1755-0998.2008.02359.x

Zhu, H., Wu, X., Shao, M., Wang, C. and Zhu, J., 2010. Selection of the captive-bred Chinese alligators (Alligator sinensis) for wild releasing based on microsatellite loci analysis. J. appl. Anim. Res., 38: 85–87. https://doi.org/10.1080/09712119.2010.9707161

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