Phylogeography, Population Genetics, and Conservation of Javan Gibbons (Hylobates moloch)
The island of Java is heavily populated (density of >1000 people/km2) and natural forest is found only scattered on many of the higher mountains. Forest loss reached its peak between 1850 and 1900, and although conversion and degradation have steadily reduced the available forest further, the pattern of forest fragmentation has remained fairly stable since (Koorders 1912; Whitten et al.1996). As such, forest-dependent species, including the endemic Javan gibbon (Hylobates moloch), have been confined to isolated forest fragments for longer periods than many tropical species (Smith et al.2017). This pattern of long-term fragmentation and isolation; the presence of relatively large (>500 individuals), intermediate (50–500 individuals), and small (<50 individuals) populations; and their extreme dependence on closed-canopy forest make the Javan gibbon a good model to study the population (conservation) genetics of tropical forest-dwelling species in a changing landscape.
We have concerns regarding Kheng et al.'s (2018) sampling and analysis strategies, which, when taken into consideration, result in a distorted view of the phylogeography and population genetics structure of the Javan gibbon. Adding available information about the sampling locations shows that twice the number of areas were sampled than in the analysis of Kheng et al. (2018), that there is a clear case of Isolation by Distance (IBD), and that there is no support for multiple ESUs.
Genetic Variability at the Population Level
Kheng et al. (2018) state that the exact sampling location was unknown for 21 of the 47 samples, although the sampling area was known. In fact, these locality data are available in an earlier paper, first presented in 1997 (Supriatna et al.1999), thus contradicting the statements of Kheng et al. (2018) that the samples were collected in 1999. The CITES permit linked to the import of these Javan gibbon samples into the United States (Andayani et al.2001; Kheng et al.2018) was used in or before 1996. Supriatna et al. (1999) predominantly uses the same data set as Kheng et al. (2018) and provides the pet names, sample locations, and genetic analyses for 15 of the 21 unidentified gibbons. This, with additional locality data available on the NCBI GenBank website, allows us to match individual genetic samples to their sampling locations, which in turn allows us to consider IBD (Meirmans 2012).
Samples from HLM comprise gibbons from Mts. Halimun–Salak National Park (Ciguha, Cimalang, Kenteng) and from Bayah, Pelabuan Ratu, and Jampang regencies south and southeast of Halimun (Fig. 1). All these regencies have isolated lowland forest areas including several with gibbons and are separated from the forest of Mts. Halimun–Salak by tens of kilometers of cultivated and developed land. Their isolation from the Mts. Halimun–Salak forests was already very pronounced in 1891 (Koorders 1912). None of these isolated forests cluster with Halimun, and Jampang is equidistant from Mts. Halimun–Salak, Mt. Gede–Pangrango, and Mt. Tilu.
GP contains samples from Mt. Gede–Pangrango and Telaga Warna–Megamendung, but these areas have been isolated by the heavily developed Puncak Pass for decades.
Samples from MST are indeed from Mt. Masigit (Cirata) and Mt. Simpang (Cidaun, Sindangbarang) but also from Mt. Papandayan (Margamulia), ca. 30 km to the east of Mt. Simpang. The forest on Mt. Masigit has been isolated from Mt. Simpang and Mt. Papandayan since at least 1891 (Koorders 1912).
One of the two samples from SLMT is indeed from Mt. Slamet (Purbalingga) but the other is from Mts. Dieng (Linggoasri), ca. 40 km to the east. The forests on Mt. Slamet and Mts. Dieng were continuous in 1891, but were clearly separated by 1963 (van Steenis and Schippers-Lammertse 1965).
Conversely, the forests on Mt. Halimun and Mt. Salak, both part of Mts. Halimun–Salak National Park, are still connected, with several gibbon groups present in the connecting forest corridor (Nijman 2015).
The number of private haplotypes that were limited to single populations is underestimated (their Table II).
Differences in population haplotype diversity are overestimated, as some of the most diverse areas comprise multiple isolated populations (their Table II).
Area explains a lower level of molecular variance than Kheng et al. (2018) estimate (their Table V), because several of the areas comprise multiple isolated populations.
Pairwise fixation index Fst and Jost’s index of genetic differentiation D (their Table VI) change, because these depend on the identification of areas, and comparisons between areas that are in fact contiguous (parts of HLM and SLK) or that comprise multiple long-term isolated populations (MST) are not meaningful.
The assumption of 6 populations by Kheng et al. (2018), whereas realistically there were 12, make it difficult to meaningfully interpret the output of their STRUCTURE analyses (Pritchard et al.2000), because the accuracy of STRUCTURE is affected by IBD (Meirmans 2012), and by uneven sampling (Puechmaille 2016).
In analyses that did not consider populations, such as observed heterozygosity for each locus across populations (Table III in Kheng et al.2018), genetic polymorphism using SNPs, and nucleotide diversity in noncoding regions (their Table IV), the findings as reported by Kheng et al. (2018) are unaffected.
Phylogeography and Isolation by Distance
With a better understanding of the origin of most samples, we can calculate the geographic distance between any two samples and relate that to their genetic distance. We used a Generalized Additive Model (gamlss package in R) and selected a power exponential distribution to describe the IBD relationship based on the AIC (R2 = 0.19, ΔAIC = 114 in relation to the null model; estimate: 0.03, SEM = 0.003, t-value: 7.89, P < 0.0001). There is a strong correlation between genetic distance in the mtDNA control region between two gibbons and the straight-line geographic distance between the locations where they were sampled (Fig. 1). IBD is a simple consequence of limited dispersal and individuals (and populations) that are geographically close tend to be genetically more similar than individuals (and populations) that are far apart. Sex-biased dispersal may result in different levels of genetic structure in markers with different inheritance patterns (e.g., mtDNA vs. nDNA) and the sex that disperses less tends to present a stronger overall genetic structure. In gibbons, males and females disperse over similar distances (typically one, two, or three home ranges), making the choice of markers to tests IBD less important than in species with sex-biased dispersal. Under drift and short-range gene flow, genetic similarity for neutral loci declines with geographic distance, and IBD can be easy to conflate with population structure (Meirmans 2012). Thus, genetic similarities between close populations do not necessarily reflect selection.
Implications for the Conservation Genetics of Javan Gibbons
With respect to the conservation and management of Javan gibbons, the most encouraging aspect of the Kheng et al. (2018) study is that levels of genetic variation in mtDNA and nDNA are comparable to those of other gibbons, and that there is no indication of a substantial loss of nDNA variation in the species as a whole. A model of the likelihood of survival of three large Javan gibbon populations (Ujung Kulon, Mts. Halimun–Salak, and Mts. Dieng) found that inbreeding depression (3.14 lethal equivalents per diploid genome on juvenile mortality) had no measurable effect on extinction risk in the medium–long term (100 years) (Smith et al.2017). Supriatna et al. (1999) and Andayani et al. (2001, p. 774) noted that “releasing confiscated gibbons … into the wild population on Java should be avoided except under the most stringent conditions of taxonomic identification.” However, Javan gibbons have been released in at least five areas in recent years, viz. Takokak, Mt. Tilu, Mt. Malabar, Mt. Gede, and Mt. Pangrango. These released gibbons comprise a mixture of confiscated wild-caught, captive-born, and captive-bred individuals predominantly from Java, but also from zoos outside Indonesia. As far as we are aware, no genetic tests have been conducted to assess the geographic origin, or the putative ESU, of these released individuals or their parents. While this may augment gene flow, in the absence of any evidence of inbreeding depression in Javan gibbons, it is doubtful whether or not populations would benefit from this.
Given our alternative interpretation of the data presented by Kheng et al. (2018), there is currently not enough support to justify an ESU-level management strategy for conservation practices. Increased sampling of known localities would provide clearer evidence for/against the existence of ESUs and their potential role in conservation management of the Javan gibbon.
We thank the reviewers and the editor for helpful comments and suggestions for improvement, Valentine Kheng for informing us about her studies, and Thais Morcatty for help with the analysis.
- Koorders, S. H. (1912). Excursion flora von Java. Jena. Fischer.Google Scholar
- Nijman, V. (2015). The silvery gibbons in mount Halimun-Salak National Park, Java, Indonesia. In H. Rainer, A. White, & A. Lanjouw (Eds.), State of the apes: Industrial agriculture and ape conservation (pp. 221–227). Cambridge: Cambridge University Press.Google Scholar
- Pritchard, J. K., Stephens, M., & Donnelly, P. (2000). Inference of population structure using multilocus genotype data. Genetics, 155, 945–959.Google Scholar
- Supriatna, J., Andayani, N., Forstner, M., & Melnick, D. J. (1999). A molecular approach to the conservation of the Javan gibbon (Hylobates moloch). In J. Supriatna & B. A. Manullang (Eds.), Proceedings of the international workshop on Javan gibbon (Hylobates moloch): Rescue and rehabilitation (pp. 25–31). Jakarta and Depok: Conservation International Indonesia and University of Indonesia.Google Scholar
- Van Steenis, C. G. G. J., & Schippers-Lammertse, A. F. (1965). Concise plant-geography off Java. In C. A. Backer & R. C. Bakhuizen van den Brink (Eds.), Flora of Java (Vol. 2, pp. 1–72). Groningen: Noordhoff.Google Scholar
- Whitten, A. J., Soeriaatmadja, R. E., & Affif, S. (1996). The ecology of Java and Bali. Singapore: Periplus Editions.Google Scholar