Phylogeography of the Golden Jackal (Canis aureus) in India

The golden jackal (Canis aureus) is one of the most common and widely distributed carnivores in India but phylogeographic studies on the species have been limited across its range. Recent studies have observed absence of mitochondrial (mt) DNA diversity in European populations while some North African populations of golden jackal were found to carry gray wolf (Canis lupus lupaster) mtDNA lineages. In the present study, we sequenced 440 basepairs (bp) of control region (CR) and 412 bp of cytochrome b (cyt b) gene of mtDNA from 62 golden jackals sampled from India (n = 55), Israel (n = 2) and Bulgaria (n = 5), to obtain a total of eighteen haplotypes, comprising sixteen from India and one each from Israel and Bulgaria. Except for three previously described haplotypes represented by one cyt b and one CR haplotype both from India, and one CR haplotype from Bulgaria, all haplotypes identified in this study are new. Genetic diversity was high in golden jackals compared to that reported for other canids in India. Unlike the paraphyletic status of African conspecifics with the gray wolf, the Indian (and other Eurasian) golden jackal clustered in a distinct but shallow monophyletic clade, displaying no evidence of admixture with sympatric and related gray wolf and domestic dog clades in the region. Phylogeographic analyses indicated no clear pattern of genetic structuring of the golden jackal haplotypes and the median joining network revealed a star-shaped polytomy indicative of recent expansion of the species from India. Indian haplotypes were observed to be interior and thus ancestral compared to haplotypes from Europe and Israel, which were peripheral and hence more derived. Molecular tests for demographic expansion confirmed a recent event of expansion of golden jackals in the Indian subcontinent, which can be traced back ~ 37,000 years ago during the late Pleistocene. Our results suggest that golden jackals have had a potentially longer evolutionary history in India than in other parts of the world, although further sampling from Africa, the Middle East and south-east Asia is needed to test this hypothesis.

Introduction [15]. Hitherto regarded as a species of low conservation significance and therefore meriting limited genetic investigations, these recent studies underscore the need for genetic studies to understand the phylogeography and diversity of golden jackals throughout their extant range.
In this paper, we present to our knowledge a first assessment on the genetic variability of the golden jackal populations in India. The Indian golden jackal populations are important for investigating phylogeography in the species as they encompass a major central portion of their global distribution. This study used mtDNA sequences to explore the following themes with regard to golden jackal systematics and phylogeography in India-(i) genetic diversity among golden jackal populations in India, (ii) signatures of population change, and (iii) relationships to wolves and other wolf-like canids in the region and across their range.

Ethics Statement
Samples were collected from road-killed individuals and from golden jackals that were captured for a radio-telemetry study in Gujarat. Golden jackals were captured using a rubber padded "soft catch" foot hold trap and subsequently anesthetized using a gas powered dart delivery system with a combination of 8mg/kg ketamine and 2mg/kg xylazine [16]. Blood samples were drawn by a qualified veterinarian and jackals were cared for till total recovery from anesthesia, released at the capture site and subsequently monitored through radio-signals to ensure their well-being. Capture permits were obtained from the Chief Wildlife Warden as per the Wildlife (Protection) Act 1972. Canis aureus is listed in schedule III of this Act, and as species of least concern by the IUCN red list. This research project was conceived and radio collaring of jackals was done prior to the formation of an animal ethics committee at the Wildlife Institute of India. The research was approved by the Training and Academic Council (TRAC) of the Wildlife Institute of India which is composed of experienced wildlife biologists, academicians, wildlife managers, the dean and director of the Wildlife Institute. The TRAC approves research proposals based on their scientific merit and value for conservation. Use of soft catch leg-hold traps, capture techniques and anesthesia for canids were approved by TRAC and the Chief Wildlife Warden. Smithsonian Institution scientists were not involved in the field ecology study and were subsequently involved in study design and training of two student co-authors in the genetics portion of the study. Furthermore, none of the samples were processed in the genetics lab at the Smithsonian Institution. All laboratory analysis was done at the Conservation Genetics laboratory of the Wildlife Institute of India. Samples from Bulgaria and Israel were provided by Ivan Nikolov (Technical University Munich, Germany) and Dr. Eli Geffen (Tel Aviv University, Israel) respectively.

Sampling and Laboratory work
Tissue (n = 31) and hair samples (n = 7) were obtained opportunistically from road-killed individuals of golden jackal from across northern, western and peninsular India between the years 1994 to 2012 (S1 Table and S1 Fig). Blood samples (n = 11) were obtained from golden jackals that were captured for a telemetry study in Gujarat in western India. Two samples from Israel and five samples from Bulgaria were also obtained for analyses. Samples were collected in 15 ml polypropylene screw cap tubes containing 70% ethanol in field and stored at -20°C upon arrival at the lab. Total DNA was extracted using the DNeasy extraction kit (QIAGEN Ag., Germany). We amplified approximately 440 bp region of the mtDNA CR locus using the primer pairs ThrL15926 and DL-H16340 [17]; and a 412 bp fragment of the mtDNA cyt b gene using a canid specific light primer (Canid L1, [18]) and universal heavy primer (H15149, [19]). Polymerase chain reactions (PCRs) were carried out in a volume of 25 μl including 0.5 units of AmpliTaq Gold (Applied Biosystems Inc., USA), 1X PCR buffer, 2.0 mM of MgCl2, 0.2 mM of each deoxynucleoside triphosphate, 0.5 μM of each primer, and 100-200 ng of template DNA. The thermocycling parameters were-initial denaturation at 95°C for 15 minutes, followed by 35 cycles at 94°C for 30 seconds, 55°C for 30 seconds and 72°C for one minute, and a final elongation step at 72°C for ten minutes. PCR products were cleaned using ExoSAP (GE Healthcare, USA) and sequenced in both directions using the BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems Inc., USA) according to the manufacturer's instructions. DNA sequences were resolved on the ABI Prism 3130 Genetic Analyzer (Applied Biosystems Inc., USA). All sequences obtained from this study were aligned by eye in Sequencher 4.6 (Gene Codes Corporation Inc., USA), and deposited in GenBank under the accession numbers (KT343779 -KT343803, see S1 and S2 Tables).

Data Analyses
To understand evolutionary relationships of golden jackals with other Canis sp., we performed a Bayesian Markov Chain Monte Carlo (MCMC) sampling scheme in MrBayes v3.2.2 [20] by using the concatenated fragment of the mtDNA cyt b (332 bp) and CR (277bp) sequences of golden jackals generated in this study, and including corresponding sequences of other wolflike canids available in GenBank. Maned wolf (Chrysocyon brachyurus) sequence was used as outgroup to root the tree. The run length consisted of a total of 2 million MCMC replicates, of which the first 0.5 million runs comprised the burn-in, and chain convergence was assessed from the average standard deviation in split frequencies (<0.01). Gaps were treated as missing data and not used in analysis. Trees were analyzed using the Hasegawa-Kishino-Yano (HKY, [21]), general time reversible (GTR, [22]), Felsenstein 1981 (F81, [23]) and mixed models of molecular evolution implemented in Mr Bayes. We analyzed the outputs of MrBayes runs using Bayes Factors [24] to obtain estimates of probabilities for the best model of molecular substitution for our data (S3 Table). The GTR substitution model with a gamma distributed rate variation and having a proportion of invariable sites (GTR + invgamma) was found to be the most likely model (Model Probability = 0.981) compared to all other models tested (Model Probability < 0.02) in this study. We used MEGA 6 [25] to estimate mtDNA cyt b and CR genetic distances between species, by applying the Tamura-Nei model [26] and a Gamma distribution parameter of 0.3 as in Sharma et al. [27]. All gaps were treated as missing data and removed from analysis using the conservative Complete-Deletion option in MEGA. Standard error was estimated using 1,000 bootstrap replicates. To examine potential regional genetic structure, a median joining network tree [28] of mtDNA haplotypes was constructed using the program NETWORK 4.613 (http://www.fluxus-engineering.com, Accessed 20 June 2015). Network calculations were carried out by assigning equal weights to all variable sites and with default values for the epsilon parameter (epsilon = 0) in order to minimize alternative median networks. Gaps were treated as missing data and nucleotide alignment blocks containing indels were removed before analysis.
We used Arlequin v3.1 [29] to calculate the number of polymorphic sites (S), nucleotide (P) and haplotype diversity (h). Nucleotide diversity is the average number of nucleotide differences per site and h is the probability that any two randomly sampled haplotypes are different [30]. Signatures of population expansion, equilibrium or decline in golden jackals were inferred from Tajima's D [31] and Fu's F S [32] statistics, and mismatch distribution tests [33] were computed in DnaSP v.5.10 [34] and Arlequin v3.1 [29] using mtDNA CR sequences. Tajima's test is based on average pairwise differences between sequences arising from the number of segregating polymorphic sites (S). Tajima's D statistic is a measure of the observed variation seen in a population with respect to variation expected in a randomly evolving population at drift-mutation equilibrium. If the variation is selectively neutral and populations are at equilibrium, Tajima's D will be indistinguishable from zero. On the other hand populations which experienced a contraction will have positive value of D (too few segregating sites/too many pairwise differences). D will be negative in populations which are undergoing demographic expansion or mutational selection (too many segregating sites/too few pairwise differences). The related Fu's F S statistic measures the discrepancy between nucleotide differences observed in the sample, compared to the distribution expected in a randomly evolving selectively neutral sample at population equilibrium. A significantly negative value of Fu's F S statistic indicates recent demographic expansion or departure from the null model hypothesis of selective neutrality and population equilibrium. The P-value is obtained from the proportion of random F S statistics to the observed F S value. Mismatch distribution tests detect patterns of variation of observed sequence differences to that expected in a randomly neutral population at drift-mutation-equilibrium. Populations that have experienced a recent expansion typically produce a right-skewed unimodal peak, whereas ragged and multimodal distributions are symptomatic of populations at demographic equilibrium [33]. To calculate the estimated time since expansion (t), the parameter Tau (T)τ was estimated from mismatch distributions of pairwise differences among golden jackal haplotypes, and the formula T = 2μt was rearranged to calculate t, where μ is the mutation rate of the control region in units of per base pair per generation. We used a mutation rate (μ) of 7.30 x 10 −5 bp -1 yr -1 as previously applied to CR sequences in the gray (Urocyon cinereoargentus, [35]) and red fox (Vulpes vulpes, [36]). A generation time of one year was chosen based on the age of sexual maturity or first reproduction which is about eleven months in golden jackal [37].

Results
A total of eighteen CR haplotypes comprising sixteen from India, and one each from Israel and Bulgaria, were obtained from CR sequences of 58 golden jackals (56 from this study and two from GenBank) from India, the Middle East and Europe (Fig 1 and Table 1). In contrast, cyt b showed lower genetic diversity compared to CR sequences, with only nine haplotypes being obtained from a total of 40 cyt b sequences of golden jackal from India, Israel and Bulgaria. Seven cyt b haplotypes (six from this study and one from GenBank) were found in India (Table 2). CR and cyt b haplotypes from India were not present in Bulgaria or Israel, and viceversa. All haplotypes sequenced in this study are new and not previously described in Gen-Bank, except the Bulgarian CR haplotype which is identical to a previously published European haplotype sequence [7,9,38], and one cyt b and CR haplotype each from Central India [39]. All the Indian, Bulgarian and Israeli haplotypes formed a monophyletic clade within the golden jackal lineage which was strongly supported (posterior probability = 1.00) in the Bayesian phylogenetic analysis (Fig 2). The Indian golden jackal haplotypes clustered in a shallow monophyletic group, distinct from related wolf and domestic dog lineages in the Indian subcontinent (Fig 2). Average Tamura-Nei + G genetic distances between the golden jackal and other Canis sp. showed high divergence at both cyt b (>5%) and CR (>10%) sequences ( Table 3). The taxa closest to C. aureus are Ethiopian wolf (C. simiensis, 5.3% and 19%), coyote (C. latrans, 5.8% and 18.9%), Himalayan wolf (C. l. chanco, 5.3% and 12.9%) and peninsular Indian wolf (C. l. pallipes, 5.6% and 16.5%), based on cyt b and CR sequences respectively. Average cyt b and CR distances between golden jackal and the wolf-dog clade was slightly higher (8.2% and 15.1% respectively). Besides these relationships to previously recognized wolves from various parts of the globe, we also compared sequences of canids recently proposed to represent African wolves (C. lupus lupaster, 5.2% and 17.2% for cyt b and CR respectively) which were previously classified as golden jackals [11].
The median joining cyt b haplotype network showed a shallow star-like radiation, and with individual haplotypes differing from each other by one to two nucleotide bases (Fig 3). On the other hand, the CR haplotypes revealed a weakly structured haplotype network with multiple alternative connections, and with haplotypes being separated from one another by one to three base substitution events (Fig 4). A similar pattern was also visible in the network analysis of the concatenated cyt b and CR haplotype sequences (S2 Fig). However, unlike the predominantly single base separation of individual cyt b and CR haplotypes, most haplotypes were separated from neighboring haplotypes by at least two or more base substitutions. Sixty one percent (11 of 18) of the CR haplotypes are completely peripheral with only one connection to the network (Fig 4). All interior haplotypes were represented by Indian samples. Haplotypes from Bulgaria and Israel were peripheral compared to Indian haplotypes and separated from Indian jackals by one and two base substitutions respectively (Fig 4). The north Indian CR haplotype CauInd11, represented by one jackal sampled in Uttar Pradesh, was the most interior in the network with six connections to other haplotypes (Fig 4). Haplotypes CauInd01, CauInd07, CauInd08 and CauInd15 obtained from golden jackal samples in northern and western India, each had four connections to the remaining haplotypes in the network (Fig 4). Although the phylogenetic trees and median joining network revealed a lack of genetic structure in Indian  [11,12,13], which observed cryptic speciation or introgression of gray wolf mtDNA lineages within golden jackals and wolf-jackal hybrid phenotypes, implying that the African wolf (gray wolf mtDNA clade) likely co-occur in the same area as the golden jackal in Africa. The golden jackal distribution map was obtained as a shape-file from the IUCN species database (http://maps.iucnredlist.org/map.html?id=3744, Accessed 4 June 2014), while the base geographic layer was downloaded from the NaturalEarth database (www.naturalearthdata.com, Accessed 4 June 2014).

Discussion
In this study, we sequenced a 440 bp fragment of the noncoding mtDNA CR locus and 412 bp of the coding mtDNA cyt b gene to study the phylogeography of golden jackal in the Indian subcontinent. MtDNA is inherited from the female parent as a single linkage unit, and has a mutation rate that is five to ten times higher than the average rate of synonymous substitutions at single-copy protein nuclear genes in mammals [40]. Furthermore, variable segments within the non-coding CR segment evolve about four to five fold faster that the entire mtDNA molecule [40]. Hence, due to its high mutation rates, small size and conserved arrangement of genes, mtDNA is extensively used to study phylogeography across many vertebrate species [41]. The phylogenetic analysis of golden jackal and related Canis sp., including the African wild dog (Lycaon pictus), dhole (Cuon alpinus) and maned wolf as outgroups, supports similar relationships of this group of Canis as previously reported by Lindblad-Toh et al. [42], Rueness et al. [11] and Gaubert et al. [12]. Golden jackals from India, the Middle East and Europe formed a monophyletic clade, which was highly divergent from other canid species (cyt b genetic distance >5%). The cyt b gene is commonly used as a genetic marker to distinguish among mammalian species, and >5% sequence divergence is typically observed between Table 3. Mean Tamura-Nei + G genetic distances among the main Canis lineages and other wolf-like canids, estimated from cytochrome b (below diagonal) and control region (above diagonal) sequences. Values in square brackets represent standard error estimates. Depicted taxa include golden jackal (GJ), African wolf (AW), wolf-dog clade (WDC), Indian wolf (IW), Himalayan wolf (HW), coyote (CY), Ethiopian wolf (EW), black-backed jackal (BBJ), side-striped jackal (SSJ), dhole (DL), African wild dog (AWD) and maned wolf (MW). Distance not estimated (ne) as CR sequence of BBJ is not available. morphologically recognized species [43]. Despite the high degree of morphological and behavioural similarity of black-backed (C. mesomelas) and side-striped jackals (C. adustus) to golden jackals [36], they are not closely related to each other (>10 to 20% cyt b genetic distances). The paraphyletic origins of the jackal group have also been reported by previous studies on canid systematics [10,11,12,13,42]. Although sequence divergence was high (>5% cyt b genetic distance), golden jackals formed a sister clade with the Ethiopian wolf, albeit with low phylogenetic support (Bayesian posterior probability < 0.90). Phylogenetic support was similarly low (Bayesian posterior probability < 0.90) at the fork leading to the divergence of the archetypal wolf clades (gray, Indian, Himalayan wolf and domestic dog lineages) from the neighbouring clade represented by the coyote, Ethiopian wolf and golden jackal. However, the evolutionary relationships among these group of Canis species have been well established [10,42] and the low nodal support values observed in our analysis is likely an artifact of using short DNA sequences for phylogenetic alignment in this study. The phylogenetic analysis revealed a polytomy and no clear pattern of genetic structure between Indian, Israeli, Bulgarian and previously published haplotypes (Fig 2). We excluded African golden jackal haplotypes from Kenya [10] in our analyses due to the questionable Haplotype circles are colour coded according to geographic locality, and circle size is proportional to haplotype frequency. Each node represents a one base pair change. See Table 1    Phylogeography of the Golden Jackal nature of these sequences as highlighted by Rueness et al. [11] and Gaubert et al. [12], which revealed these sequences to closely resemble the side-striped jackal (Canis adustus) and not golden jackal. Unlike the noticeable incidences of hybridization between golden jackal and gray wolf observed in the African golden jackal/ wolf (Canis lupus (aureus) lupaster) in western and northern Africa [11,12] and to a lesser extent in Europe [14], there was no evidence in our data to suggest mtDNA gene flow between the golden jackal and with other related Indian, Himalayan and wolf-dog clades in India. Although there is some indication that golden jackals can breed with domestic dogs in captivity [44] and anecdotal accounts exist of Indian feral dogs which are strikingly similar to jackals [45], we detected no evidence of hybridization in our study. However, our sampling was opportunistic and limited in scale for a conclusive study on hybridization between the different Canis species in India. The ranges of golden jackal and gray wolf overlap greatly not just in India, but also in southern Asia, the Middle East and the Balkans. Hybridization between jackals and wolves (and presumably feral dogs as well) may occur, especially in localities where population depletion has led to reduced mate availability in the wild. Extensive sampling of golden jackals, wolves and feral dogs, especially around areas of ecological overlap and contact zones from throughout the Indian subcontinent, is required to detect any incidence of potential admixture in this region. Furthermore, information from biparentally inherited nuclear markers is required as mtDNA sequencing can only reveal maternal genetic history. Further studies using autosomal nuclear markers (microsatellites and SNPs) and Y-chromosome linked markers are needed to evaluate the population structure, demographic history and potential hybridization with other canid species in the region.
Our results show that golden jackal populations in India exhibit high haplotype diversity, with no clear phylogeographic breaks and likely have undergone recent demographic expansion. Six of the seven cyt b haplotypes and fifteen of sixteen CR haplotypes found in India were novel and have not yet been reported for other golden jackals published in GenBank. No clear phylogeographic pattern in India could be inferred from analysis of cyt b and CR haplotypes. Since cyt b had low resolution and revealed a polytomy as evidenced by the shallow star-like radiation in the median-joining network (Fig 3), we attempted to resolve the phylogeographic patterns using the more variable CR fragment of the mtDNA genome. In the few instances where CR haplotypes were shared between localities, they were not always shared with jackals from the same geographic region (Figs 1 and 4) and the level of resolution of the phylogenetic tree did not reveal any clear phylogeographic breaks (Fig 2). Lineage interpretation was confounded by multiple alternative connections across some haplotypes that are equally parsimonious, which could be due to homoplasy caused by the high mutation rate of the control region [41] and rapid expansion of the golden jackal populations due to high dispersal ability [3,4]. In contrast, the cyt b network showed a clear radiation of European and Middle Eastern haplotypes from India, compared to the intermingled CR network. Assuming that the ancestral haplotypes are internal while the derived haplotypes are peripheral, the CR haplotype CauInd11 with six connections to other haplotypes, and CauInd01, CauInd07, CauInd08 and CauInd15 with four connections, are relatively ancestral compared to the remaining haplotypes. These basal haplotypes were restricted to western and northern India and absent from other sampled regions. In contrast, CR haplotypes sampled from southern (CauInd09) and central India (CauInd10, CauInd14 and CauInd16) in our study were observed to be localized and more derived relative to northern and western Indian haplotypes. The most widespread Indian haplotype is CauInd01, represented by eight individuals from western (Gujarat, Rajasthan) and northern (Uttar Pradesh) India. CauInd11 with six connections is the most ancestral haplotype sampled in our study. Due to low sampling intensity across India (except Gujarat state in western India) it is quite likely that more ancestral haplotypes may as yet be unsampled. The evidence of extensive branching, existence of alternative connections and shallow divergence seen in the golden jackal haplotype network is indicative of a population that has recently undergone demographic expansion. Indian CR haplotypes are not monophyletic with respect to other haplotypes found in GenBank [7,39] and sequenced from Israel and Europe in this study. The high haplotype diversity at the CR locus for Indian golden jackal populations contrasts with the monomorphic CR haplotype consistently observed in Bulgarian and neighbouring Balkan populations in south-eastern Europe [7,9]. Our findings of high haplotype diversity in Indian golden jackals dispel the notion of mtDNA CR monomorphism in European populations having arisen from exceptionally conserved molecular dynamics, but rather from a signature of recent expansion in the area [9]. The dominant presence of this monomorphic haplotype in Europe could have resulted from a few long-distance dispersers at the leading edge of an expansion event which colonize a new area, leading to modern signals of reduced genetic diversity [46]. A similar pattern is also observed in the widespread Himalayan wolf (C. lupus chanco) mtDNA haplotype C lineage which is present in a wide-arc from Kashmir to eastern Nepal [23].
Signatures of demographic expansion or selection in the Indian golden jackal populations are evident from both Tajima's D and Fu's F S test statistics which are negative and in the mismatch distribution of pairwise differences which produced a right-skewed unimodal peak characteristic of demographic expansion. The non-significance of observed test statistics is likely due to the low sample sizes across many haplotypes. By using estimates of mutation rate previously applied in related species [35,36], to a simple coalescence equation, we timed the start of the demographic expansion seen in the Indian jackal populations to almost 37,083 YBP (90% CI: 16,133-71,249). Golden jackals from Europe, Israel and the entire Eurasian population (including India) were dated to expand much later~20,548 YBP (90% CI: 2,649-23,973). These expansion dates coincide with the estimated periods of the inter-glacial cycles of the late Pleistocene, wherein certain relatively warmer areas in India and south-east Asia were believed to have served as refugia during the last glacial maxima~18 000 to 25,000 years ago [47,48]. The presence of refugial populations in the Indian subcontinent during the Pleistocene glaciations is also corroborated by the existence of unique wolf lineages in the region which are basal and divergent from all other widespread wolf-dog clades [27]. However, it has been demonstrated that mtDNA polymorphism can be generated much before sister populations diverge [49], so our estimated time of expansion is probably an overestimate of the time of split. This could be the case with golden jackal colonization over many parts of Europe which appear to be of recent origin, although the estimate assumes that the present haplotypes have evolved in the region 20,458 years ago to the observed composition and frequency. It is more likely that the European populations harboring this unique haplotype at the northern extremity of golden jackal range, evolved from southern refugial populations which later expanded into the region. Records suggest that much of the sampled European populations were founded by migrants in recent decades, owing to habitat related changes and the extirpation of wolves from the area [4,9].
Our study showed that haplotype diversity in the golden jackal was much higher than in any other member of the genus Canis surveyed to date in India. Only four CR haplotypes were recovered for peninsular Indian wolf, five for Himalayan wolf and eleven for C. lupus familiaris [27]. In addition, only one cyt b haplotype was found when sequencing multiple individuals from different localities for each of these species [27]. However, cyt b sequences of Indian jackals revealed seven different but closely related haplotypes throughout the region, only differing by one or two base substitutions from one another (Fig 3 and Table 1). This suggests that golden jackals have high levels of mtDNA diversity compared to all the other Canis sp. that inhabit this part of the world including feral and domestic dogs. It also suggests that historically golden jackals have had large effective population sizes and a potentially longer evolutionary history in India than in other parts of the world, although further sampling from Africa, the Middle East and south-east Asia is needed to test this hypothesis. Past geological events in the Indian subcontinent may have shaped the current phylogeographic distribution of golden jackals that we observe today. However, current understanding of golden jackal evolutionary history based on genetic data alone, as presented in this study cannot predict a narrow enough time frame for expansion as it encompasses a wide interval (16,133 to 71,249 YBP). The post-Pleistocene expansion from refugial populations in the Indian-subcontinent to neighbouring regions seems likely as attested by the negative Tajima's and Fu's test statistics and right-skewed mismatch distribution peak. The star shaped polytomy of the haplotype network suggest that golden jackals may have undergone dramatic demographic changes in the recent past. Based on currently available data the Indian-subcontinent seems to be the center of radiation of golden jackals.   Table. Best model selection. Estimating the best model of molecular substitution inferred using Log Bayes Factors (LBF) from Bayesian posterior distributions in Mr Bayes. Rate variation for tested models-gamma distributed rate variation across sites (gamma); gamma distributed with proportion of invariable sites (invgamma); rate variation with proportion of invariable sites (propinv); equal rate variation across sites (equal). (DOCX)