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ORIGINAL RESEARCH article

Front. Genet., 01 November 2021
Sec. Evolutionary and Population Genetics

Distinct Genetic Structure Reflects Ploidy Level Differentiation in Newly Discovered, Extremely Small Populations of Xanthocyparis vietnamensis from Southwestern China

Yuliang Jiang,&#x;Yuliang Jiang1,2Tsam Ju&#x;Tsam Ju2Linda E. NeavesLinda E. Neaves3Jialiang LiJialiang Li2Weining TanWeining Tan4Yusong HuangYusong Huang1Yan Liu
Yan Liu1*Kangshan Mao
Kangshan Mao2*
  • 1Guangxi Key Laboratory of Plant Conservation and Restoration Ecology in Karst Terrain, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, Guangxi Institute of Botany, Guilin, China
  • 2Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, State Key Laboratory of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, China
  • 3Fenner School of Environment and Society, Australian National University, Canberra, ACT, Australia
  • 4Administration of Mulun National Nature Reserve of Guangxi, Huanjiang, China

Population genetic assessment is crucial for the conservation and management of threatened species. Xanthocyparis vietnamensis is an endangered species that is currently restricted to karst mountains in southwestern China and Vietnam. This rare conifer was first recorded in 2002 from northern Vietnam and then in 2013 from Guangxi, China, yet nothing is known about its genetic diversity nor ploidy level variation, although previous cytological study suggest that Vietnamese populations are tetraploids. There have been about 45 individuals found to date in Guangxi, China. Here, we genotyped 33 X. vietnamensis individuals using 20 newly developed, polymorphic microsatellite loci, to assess the genetic variability of its extremely small populations. The genetic diversity of X. vietnamensis (HE = 0.511) was lower than that of two other heliophile species, Calocedrus macrolepis and Fokienia hodginsii, which have similar distribution ranges. This is consistent with the signature of a genetic bottleneck detected in X. vietnamensis. Although the population genetic differentiation coefficient across loci is moderate (FST = 0.125), STRUCTURE analysis revealed two distinct genetic clusters, namely the northern and southern population groups; DAPC analysis grouped the southern populations together in one cluster separate from the northern populations; AMOVA analysis detected a significant genetic differentiation between the two population groups (FRT = 0.089, p < 0.05), and BARRIER analysis detected a genetic barrier between them. Moreover, we detected differentiation in ploidy level between northern and southern populations, sampled individuals from the former and the later are all diploid and tetraploid cytotypes with mean genome sizes of 26.08 and 48.02 pg/2C, respectively. We deduced that heterogeneous geomorphology and historical events (e.g., human deforestation, Quaternary climate oscillations) may have contributed to population fragmentation and small population size in X. vietnamensis. Considering both genetic and ploidy level differentiation, we propose that two different management units (northern and southern) should be considered and a combination of in situ and ex situ conservation measures should be employed to preserve populations of this endangered species in southwestern China in the light of our findings.

Introduction

Understanding the level and distribution of genetic variation has implications for the conservation of species and ecosystems (Bruford et al., 2017). Measures of genetic diversity are important elements for estimating species fitness and the potential for population persistence (Reed and Frankham, 2003). Generally, small population size and low gene flow among populations are associated with low genetic diversity of a species (Hamilton, 2009). Populations with low genetic diversity have a limited ability to adapt to, and survive environmental changes (Jump et al., 2009; Weeks et al., 2011), and active conservation is often needed for such populations. Thus, assessment of genetic variability is necessary for designing conservation programmes for endangered species (Yamamoto et al., 2017; Chung et al., 2020).

Many species of conservation concern are endemic, fragmented, and have limited gene flow and high level genetic differentiation among populations, which are generally attributed to cyclical climatic changes, complex geological history, and longstanding influence of human activities (González-Martínez et al., 2010; Liao et al., 2015; Li et al., 2020). Usually, high levels of endemism suggests in situ long-term survival, differentiation, and speciation (Tang 2015). For example, endangered relict plants are mostly paleoendemic, confined to a particular geographic area and, have typically been isolated for quite a long time (Hobohm, 2014). Their current distribution represents the remnants of a much larger paleo-distribution. It is a general inclination to treat endemic species as high-priority conservation targets, but conservation efforts are often faced with a dilemma (Groves, 2003; Edmands, 2007). Fragmentation of habitats is usually accompanied by reductions in population size, genetic isolation, increased inbreeding within populations, and decreases in genetic diversity (Aguilar et al., 2008). Hence, habitat fragmentation is considered one of the biggest threats to the survival of species with small and isolated populations, especially in the context of increased intensity of human activities all over the world (Hamrick, 2004; Liao et al., 2015). It is imperative to investigate the effect of habitat fragmentation on endangered relict plants.

Xanthocyparis vietnamensis Farjon & Hiep of the Cupressaceae family, was first described from the remnants of karst forests in the northern Vietnamese border in 2002, where mountainous regions were once inaccessible (Averyanov et al., 2002; Farjon et al., 2002). In recent decades, scattered individual trees of this species have been found in karst landscape in the northern and southern border counties of the Guangxi Zhuang Autonomous Region in southwestern China (Meng et al., 2013; Jiang et al., 2021). Populations in China and Vietnam are small in size (each containing 1–50 individuals) and inhabit isolated tops of steep and narrow mountain ridges, with low levels of reproduction under natural conditions (Averyanov et al., 2002; Averyanov et al., 2013; Jiang et al., 2021). According to the evaluation criteria from the 2013 International Union for Conservation of Nature and Natural Resource Red list, X. vietnamensis is classified as an endangered species (Thomas, 2013).

Although previous studies suggested that X. vietnamensis was sister to the Alaska Cedar (Callitropsis nootkatensis) and hence were placed into a genus that comprised of only these two species (Little et al., 2004; Little, 2006), another study placed X. vietnamensis, the Alaska Cedar, the New World Cypresses (Hesperocyparis) and the Old World Cypresses (Cupressus sensu strico) into a single genus (Cupressus sensu lato) (Christenhusz et al., 2011). However, recent phylogenetic and phylogenomic studies suggest that X. vietnamensis is basal, in a clade also containing the Alaska Cedar as sister to a monophyletic clade comprising all of the New World Cypresses (Hesperocyparis) (the HCX clade) (Mao et al., 2010; Mao et al., 2019); the HCX clade is then basal to a clade where the Old World Cypresses (Cupressus sensu strico) is sister to junipers (Juniperus) (Mao et al., 2019). Within the HCX clade, X. vietnamensis diverged from the other species around late Eocene (Mao et al., 2019). Although no fossil evidence exists for Xanthocyparis (sensu stricto), it is high likely that it has survived a long history of environmental changes since late Eocene, and high likely that the species had a considerably wider distribution in warmer geological periods. Hence, this recently discovered, endangered conifer merits further investigations to aid its conservation.

Recently, a ploidy screening analyses of Cupressaceae plants suggested that X. vietnamensis is tetraploid with a genome size of 44.60 pg/2C, which is unexpected considering the generally low frequency of polyploidy in extant gymnosperms (Farhat et al., 2021). However, this is based on an analysis of eight individuals collected from Vietnam. Previous studies had reported the natural intraspecific variation of ploidy level in a few gymnosperm species, such as Juniperus chinensis and J. sabina (Farhat et al., 2019). Based on our morphological observation, the scale-like leaves in X. vietnamensis individuals from northern Guangxi are always much smaller than those from southern Guangxi (Supplementary Figure S1). Since tetraploids usually possess bigger leaf size than diploids (Zhang et al., 2019), here we propose a novel hypothesis: X. vietnamensis populations in Guangxi have two cytotypes, namely diploids and tetraploids. Extensive studies are now needed to reveal the ploidy level variation within and between populations of X. vietnamensis.

Southwestern China and northern Vietnam, with their warm, humid climates and diverse topographies, have been identified as long-term climatically stable refugia likely to preserve ancient lineages, meaning these refugia may be prioritized for the conservation of relict plants (Tang et al., 2018). These regions have drawn significant attention from researchers. Conservation genetic studies have been conducted for many threatened plant species, such as Calocedrus macrolepis and Fokienia hodginsii (Liao et al., 2015; Yin et al., 2021), yet no population genetic survey has been done for X. vietnamensis. Characterizing the genetic variation in populations of X. vietnamensis is essential for effective conservation. Therefore, we used microsatellite markers to assess the levels of genetic diversity and genetic bottleneck of recently discovered populations of X. vietnamensis in southwestern China, as well as genetic differentiation and gene flow among isolated populations. We also conduct an assessment of genome size and ploidy level to understand their ploidy level variation. Our aims were to: 1) reveal the current level and distribution of genetic variation across sampled sites (individuals) in Guangxi, China, 2) identify ploidy level variation of these population and test the connection between patterns of genetic and ploidy level variations, 3) detect the effects of habitat fragmentation and isolation on genetic characteristics, and 4) provide useful insights for optimal conservation strategies.

Materials and Methods

Sample Collection and DNA Extraction

During our field survey of X. vietnamensis in Guangxi, China from 2013 to 2020, there were eight karst mountains in Guangxi where this species was found. Five and three mountains were located in the northern and southern border of Guangxi respectively (Figure 1; Table 1). Each mountain had a small number (1–20) of wild individuals growing on or near steep slopes, and the total number of individuals was approximately 45. Fresh leaves of 33 individuals were collected from six sites (mountains), immediately dried in silica gel and stored at room temperature prior to DNA extraction. Additionally, fresh and young leaves off our mature individuals were collected from each of the four sites with more than four individuals (Table 2) and kept frozen at −80°C until analyzed for ploidy level determination.

FIGURE 1
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FIGURE 1. Current distribution and leaf appearance of Xanthocyparis vietnamensisin Guangxi, China and the first discovery site in Vietnam. Population site codes: N1, N2, N3, N4, S1, S2. Insets in top middle and bottom middle show the sizes of the scale-like leaves of individuals from northern and southern Guangxi, respectively. All the karst landforms in Guangxi and partial karst landforms in the other regions are showed by the yellow marker. See a direct comparison of scale-like leaf size between individuals from northern and southern Guangxi in Supplementary Figure S1.

TABLE 1
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TABLE 1. Distribution sites of Xanthocyparis vietnamensis in Guangxi, southwestern China.

TABLE 2
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TABLE 2. Estimation of genome size and ploidy level in individuals of Xanthocyparis vietnamensis.

Sampling was limited because X. vietnamensis individuals were rare, and some individuals or sites were inaccessible (Table 1). Genomic DNA was extracted from the leaf tissue of all sampled individuals following the cetyltrimethylammonium bromide (CTAB) method (Doyle and Doyle, 1990).

Short Sequence Repeat Marker Discovery, Screening, and Data Production

Total RNA was extracted from fresh leaves of one X. vietnamensis individual for Illumina sequencing (Mao et al., 2019). The cDNA library was sequenced using the Illumina HiSeq 2000 system at Novogene (Beijing, China). Sequences were filtered, and clean reads were assembled de novo using Trinity v.2.8.5 (Grabherr et al., 2011). Short sequence repeat (SSR) of motifs were identified using the Perl script MISA (Thiel et al., 2003). Primer3 v.2.3.6 was used to design primer pairs for the detected markers (Rozen and Skaletsky, 2000; Untergasser et al., 2012). A total of 300 SSR loci were applied for pilot screening of polymorphic makers based on 16 individuals, and these polymorphic loci were then employed to detect genetic variation for all sampled individuals.

PCR amplification was performed in 25 μl reactions containing 50 ng of genomic DNA, 12.50°μl of 2× PCR buffer, 300 μM of each dNTP, 0.3 μM of primer pairs, and 1.25 U of Taq DNA polymerase (all from Vazyme Biotech, Nanjing, China). The amplification program was performed as follows: initial denaturation at 98°C for 3°min; followed by 40 cycles at 98°C for 10 s, annealing temperatures (see Supplementary Table S1) of the primer pair for 30°s, 72°C for 45°s; and a final extension step at 72°C for 10 min. Each forward primer was labeled with either FAM, HEX, and TAMRA at the 5′ extremity to allow fragment detection (Supplementary Table S1). Amplified products were inspected in a 1% agarose gel and electrophoresed on the ABI PRISM 3100 genetic analyzer (Applied Biosystems, Foster City, CA, United States). The microsatellite genotype at each locus, for each individual was determined using GeneMapper v.4.1 (Soft Genetics, State College, PA, United States). The codominant SSR data were analyzed using Cervus3.0 software (Kalinowski et al., 2007) to detect genotyping errors at each locus, such as stuttering, large allele dropouts and null alleles. When the proportion of null alleles at a locus is greater than 40% (F(Null) > 0.4), it was deemed to contain excessive null alleles. Loci were tested for natural selection using BayeScan (Foll and Gaggiotti, 2008), and the loci under selection were excluded for further population genetic analyses.

Genetic Diversity and Differentiation

The following measures of genetic diversity were calculated for each locus, population, and geographic group (south and north) using GenAlEx v.6.5 (Peakall and Smouse, 2012): number of different alleles (A), number of effective alleles (AE), Shannon’s diversity index (I), observed heterozygosity (HO), expected heterozygosity (HE), inbreeding coefficient (FIS), and genetic differentiation coefficients between groups (FST) per locus. The statistical significance of the deviation of loci from Hardy-Weinberg equilibrium (HWE) and the linkage disequilibrium test between two loci were assessed by the Markov chain method in Genepop v.4.7 (Rousset, 2008). Sequential Bonferroni correction was used to determine significance level at p < 0.05 (Rice, 1989). We also implemented hierarchical analysis of molecular variance (AMOVA) (Excoffier et al., 1992) in GenAlEx v.6.5 to calculate the level of genetic variation and differentiation among geographic groups, among populations within groups, and among individuals within populations based on F-statistics (Wright, 1978), using data of the four populations with more than one sample. The significance of the differences was tested using permutation procedures (999 replicates).

The bottleneck test for population was estimated using the M-ratio method (Garza and Williamsion, 2001), which is the ratio of the total number of alleles to the overall range of allele size. We assumed a microsatellite mutation rate per locus per generation of 10−4 and pre-bottleneck effective population size of 400 (θ = 4Neμ = 0.16) and 4,000 (θ = 1.6) to estimate the M-ratio. The mean size of non-single-step mutations and the percentage of mutations larger than a single step were set to 3.5 and 0.1, respectively (Garza and Williamsion, 2001). The M-ratio (M0) estimated using the program M_P_Val was compared to the 95% critical M-ratio (Mc) estimated using the Critical_M program. We assumed that the population experienced a significant bottleneck if M0 < Mc when Ne = 4,000, and a moderate bottleneck if M0 < Mc when Ne = 400.

Population Structure and Gene Flow

The Bayesian clustering method in STRUCTURE v.2.3.4 (Pritchard et al., 2000) was used to assess the genetic clustering of sampled X. vietnamensis populations. This analysis was run for 10 independent runs per K value (1–10) with a burn-in period of 50,000 iterations and 100,000 Markov chain Monte Carlo (MCMC) iterations, using the admixture (allele frequencies correlated) model. Structure Harvester (Earl, 2012) was used to visualize the best K value based on delta K and maximum log likelihood L(K) (Evanno et al., 2005). Discriminant analysis of principal components (DAPC) was performed to identify the differentiated subpopulations using the R package Adegenet (Jombart, 2008; Jombart et al., 2010). The number of clusters was set at 10. The microsatellite data was transform into principal components (PCs) using the function find.clusters, retaining all the PCs in the analysis. The Bayesian information criterion (BIC) was used to infer the optimal number of clusters (Jombart et al., 2010). The functions a.score and optim.a.score were applied to identify the optimal number of PCs to be retained. The function dapc performed discriminant analysis using the optimal number of PCs and four eigenvalues were retained.

MIGRATE-n (version 3.3.1) was used to estimate the mutation-scaled effective population size Θ (4Neμ; Ne, effective population size; μ, mutation rate per locus per generation), mutation-scaled migration rate M (m/μ; m, historical migration rate per generation), and the number of migrants Nm (Nem) between the two geographic groups (Beerli, 2006). We used a uniform prior distribution to estimate Θ (rang 0–80), M (range 0–300), and reported the mean and 97.5% confidence intervals for Θ and M. The starting values for Θ and M were estimated using the FST. Monmonier’s maximum difference algorithm implemented in BARRIER v.2.2 (Manni et al., 2004) was used to identify potential barriers to gene flow among populations. Nei’s distance matrices, used in determining the barriers, were produced by bootstrapping over loci with Microsatellite Analyser v.4.05 (Dieringer and Schlötterer, 2003).

Genome Size Assessment and Ploidy Level Determination

Genome size was assessed for 16 individuals of X.vietnamensis (Table 2). Relative nuclear DNA content of the individuals was estimated by propidium iodide (PI) flow cytometry using fresh leaves (Bourge et al., 2018; Farhat et al., 2021). We adopted the nuclei isolation buffer “Galbraith’s” (Galbraith et al., 1983), and samples of Cupressus funebris (2n = 22 and 2C = 21.52 pg DNA) (Hizume et al., 2001) and Pseudolarix amabilis (2n = 44 and 2C = 52.2 pg DNA) (Zonneveld, 2012) were selected as the internal calibration standards. For each sample, about 1 g of fresh leaves were placed into a glass Petri dish. Then leaves were chopped using a razor blade in 4 ml of 4°C cold buffer. The nuclear suspension was filtered through 37 or 48 μm nylon mesh. RNase A was added to the suspension to prevent staining of double-stranded RNA. Cell nuclei were stained with 100 μg/ml PI, and incubated in the dark for 30 min at 4°C before analysis by flow cytometry.

BD FACSCalibur™ Flow Cytometer (BD Biosciences, United States) equipped with a solid-state laser for PI excitation was used to detect DNA content (2C value). Three replicates were run per individual, recording at least 10,000 particles (including nuclei and fragments) per replicate. The data analysis was performed in BD CellQuest™ Pro (version 6.1). The resulting histograms were analyzed with ModFit LT 4.1.7 software. When CV values of G0/G1 peaks were below 5%, the analyses saved. The determination of ploidy level was based on the relative nuclear DNA contents and published chromosome counts (Farhat et al., 2021). The databases were accessed on August 11, 2021: Kew Plant DNA C-values database (http://data.kew.org/cvalues) and Index to Plant Chromosome Number (IPCN) (http://legacy.tropicos.org/Project/IPCN).

Results

Genetic Diversity and Genetic Structure

Twenty microsatellite markers were polymorphic in the X. vietnamensis populations analyzed in this study (Supplementary Table S1). No loci with excessive null allele and no loci under natural selection were detected. A total of 96 alleles were detected, ranging from two to ten alleles per locus, with an average of 4.8 (Table 3). The observed heterozygosity (HO) and expected heterozygosity (HE) per locus ranged from 0.156 to 0.940 and from 0.219 to 0.839, respectively. The inbreeding coefficient (FIS) per locus ranged from −0.379 to 0.575. Five loci displayed significant deviations from Hardy-Weinberg equilibrium and 10% locus pairs showed evidence of linkage disequilibrium after sequential Bonferroni correction. All loci were retained for further analysis. The genetic differentiation between the geographic groups (FST) varied among loci, ranging from 0.008 to 0.450 (Table 3).

TABLE 3
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TABLE 3. Genetic variation of 20 microsatellite markers used in this study in the population of Xanthocyparis vietnamensis in Guangxi, China.

The genetic diversity estimates at the population and group levels are summarized in Table 4. N3 had the highest HE (0.439), and N4 had the lowest HE (0.373) at the population level. At the group level, the north had a slightly higher HE (0.469) than the south (0.438). The M-ratio test for the X. vietnamensis populations detected a significant bottleneck (M0 = 0.7737; Mc = 0.7883 when the pre-bottleneck Ne = 4,000, p = 0.0326; Mc = 0.8693 when the pre-bottleneck Ne = 400, p = 0.0002).

TABLE 4
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TABLE 4. Comparison of genetic diversity of Xanthocyparis vietnamensis populations of different levels in Guangxi, China.

The STRUCTURE results showed that the L(K) continued to increase up to K = 4, and the K = 2 model received the highest delta K value (Figure 2). Histogram showing the results of K = 2 model revealed clear differences between the northern and southern populations (Figure 3). When K = 3 and 4, the N4 population separated from other northern populations, resulting in a slight signature of separation within the northern populations (Figure 3). The BIC curve in the DAPC analysis suggested that the optimal number of clusters was five (Figure 4A). The southern populations (S1 and S2) were assigned to a single cluster while the northern populations were assigned to the other four (Figure 4C). Specifically, individuals of N3 were assigned to four different clusters, and N4 were assigned to two separate clusters (Figure 4C).

FIGURE 2
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FIGURE 2. Values of the log likelihood of the data(L(K)) (mean ± SD), as a function of the number of clusters (K) resulting from the simulation in the STRUCTURE method, and delta K based on the rate of change of L(K) between successive K values.

FIGURE 3
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FIGURE 3. Histograms of the STRUCTURE assignment test for all individuals at K = 2, 3, 4. Labels on the x-axis reference to sampling site and individual (Northern sites = N1, N2, N3, N4 and Southern sites = S1, S2).

FIGURE 4
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FIGURE 4. Discriminant analysis of principal components of the microsatellite data for Xanthocyparis vietnamensis populations from Guangxi, China (A) Value of BIC versus number of clusters (B) A-score optimisation—spline interpolation (C) Scatter plots of the discriminant analysis of principal components. Each circle represents a cluster and each dot represents an individuals. DAPC assignment plot based on four discriminant functions. Eigenvalues are displayed in inset.

Population Genetic Differentiation and Historical Gene Flow

The genetic differentiation coefficient average across loci (FST = 0.125, SE = 0.025) suggested a moderate level of differentiation between the northern and southern population groups (Table 3). AMOVA showed more genetic variation was partitioned between the northern and southern population groups (6%) than among populations within groups (3%); most genetic variation was found within individuals (91%). Genetic differentiation between the northern and southern population groups (FRT = 0.089) was statistically significant (p < 0.05), while the genetic differentiation among populations and among individuals were not statistically significant (Table 5).

TABLE 5
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TABLE 5. Analysis of molecular variance (AMOVA) results of the four sub-populations (N3, N4, S1, S2).

The mean Θ values for northern and southern populations were 0.896 and 0.644, respectively. Asymmetric gene flow between north and south populations was detected, with the number of migrant individuals per generation (Nm) from south to north (0.770) being less than from north to south (2.008) (Table 6). The BARRIER analysis revealed a well-supported genetic and/or biogeographic barrier (with bootstrap support value of 75%) that separating the northern and southern populations (Figure 5).

TABLE 6
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TABLE 6. Summarized results of the MIGRATE-n analyses.

FIGURE 5
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FIGURE 5. Delaunay triangulation (in green) and Voronoï tessellation (in blue) of the barrier analyses for Xanthocyparis vietnamensis. Barriers (in dark red) are detected with bootstrap values of 100 replicates using Nei’s standard genetic distance. Red points correspond to the six sampling sites (1, N1; 2, N2; 3, N3; 4, N4; 5, S1; 6, S2).

Genome Size and Ploidy Level

The genome size estimates for the 16 individuals ranged 25.2–50.48 pg/2C. They could be distributed into two classes: Class 1 of lower values (25.42–26.50 pg/2C, mean = 26.08 pg/2C) corresponded to diploid with 2n = 2x = 22 for the individuals belonging to the northern populations, class 2 possessed higher values (46.59–50.48 pg/2C, mean = 48.02 pg/2C) corresponded to tetraploid with 2n = 4x = 44 for the individuals belonging to the southern populations (Table 2). Flow cytometric histograms obtained from analysis of two representative individuals, one each from the northern (N3-8) and southern (S1-2) populations, were shown in Figure 6.

FIGURE 6
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FIGURE 6. Flow cytometric histograms of the individuals N3-8 (A,B) and S1-2 (A, C). Xanthocyparis vietnamensis (peak 1 and 2), standard I: Pseudolarix amabilis (peak 3), standard II: Cupressus funebris (peak 4).

Discussion

Genetic Diversity of X. vietnamensis in Southwestern China

Our population genetic survey of X.vietnamensis revealed that its populations from southwestern China exhibit lower diversity (mean value across all sampled populations: HE = 0.45, HO = 0.49) than the long-lived perennial (HE = 0.68, HO = 0.63), widespread (HE = 0.62, HO = 0.57), regional (HE = 0.65, HO = 0.65) and narrow range plant populations (HE = 0.56, HO = 0.52), but exhibit higher diversity than endemic plant populations (HE = 0.42, HO = 0.32) according to the mean values provided by Nybom (2004) based on microsatellite markers. Compared with other threatened species in Southern China and adjoining areas, the diversity of X. vietnamensis (HE = 0.51, HO = 0.45) was lower than that of C. macrolepis (HE = 0.64, HO = 0.71, 291 individuals) (Liao et al., 2015) and F. hodginsii (HE = 0.64, HO = 0.52, 427 individuals) (Yin et al., 2018), yet higher than that of Glyptostrobus pensilis (HE = 0.27, HO = 0.32, 343 individuals) (Wu et al., 2020), Cathaya argyrophylla (HE = 0.41, HO = 0.37, 49 individuals) (Wang et al., 2010) and Abies ziyuanensis (HE = 0.44, HO = 0.32, 139 individuals) (Tang et al., 2008). However, although the 33 individuals sampled across the six small populations in this study represent the majority of the known distribution of X. vietnamensis in southwestern China, limited sampling still may have led to an underestimation or inaccurate estimation for the genetic diversity of this species. Moreover, our loci number may be insufficient and the population indices in Table 4 should be treated with caution.

Some relict species endemic to South China were cold-adapted, for example, C. argyrophylla and A. ziyuanensis were restricted to a few isolated alpine habitats with cold microclimates. These species tend to have lower levels of genetic variation and are faced with a greater threat of losing their last refuge in South China in the face of global warming (Tang et al., 2008). In contrast, X. vietnamensis is a heliophile and subtropical or tropical plant (Averyanov et al., 2002), similar to C. macrolepis and Pinus kwangtungensis (Tian et al., 2008), there may be a wider range of potential habitats (including non-karst montane areas) in warm South China and adjacent regions in southeast Asia. But actually it is currently inhabiting isolated mountain tops, cliffs or slopes confining within karst areas and has a very small population size that might have been partly caused by historical deforestation (Zeng et al., 2007; Wang 2011; Jiang et al., 2014). At the same time, we detected a significant bottleneck event for X. vietnamensis populations in southwestern China, when assuming two different pre-bottleneck effective population size, suggesting that this species may have experienced a strong bottleneck event in the past. This provides reasonable explanation for the low-level genetic diversity of X. vietnamensis.

Moderate Level of Population Differentiation and Significant Genetic Structure

Our population genetic survey revealed moderate genetic differentiation (FST = 0.125) among X. vietnamensis populations in southwestern China. This is similar to the mean values of anemochores (0.13) (Nybom, 2004), lower than those of F.hodginsii (0.157) (Yin et al., 2018), C. macrolepis (0.163) (Liao et al., 2015), A. ziyuanensis (0.209–0.250) (Tang et al., 2008), and G. pensilis (0.452, some populations are plantations) (Wu et al., 2020) in a similar geographic region. Varied topography of mountain regions in the tropic and adjacent areas tended to harbor Tertiary relict species and subdivide some species into isolated and divergent populations, which may have evolved independently during late Tertiary climate changes and Quaternary climate fluctuations (Hewitt, 2000; Tang et al., 2018). The karst landscape in Guangxi is a residual carbonate hill protruding from a surrounding corrosion plain (Gutiérrez and Gutiérrez, 2016). The hills are generally only hundreds of meters in height, and the nearby hill tops are generally hundreds of meters apart. Even so, the karst forest ecosystem here exhibits heterogeneous geomorphology and variegated vegetation (Su et al., 2017; Guo et al., 2018). The heterogeneous geomorphology may have contributed the genetic differentiation among populations of X. vietnamensis.

At the same time, we detected significant population genetic structure in X. vietnamensis, as both STRUCTURE and DAPC analyses clearly revealed a distinct division between the northern and southern population. In addition, a relatively strong barrier to gene flow between the northern and southern populations was identified by BARRIER analysis, and the estimated Nm from south to north or vice versa (Table 6) was limited, being consistent with the moderate genetic differentiation (Slarkin, 1985). This is supported by the fact that, there are non-karst areas between or among the karst landforms, which bear different ecological environments and interrupt the continuity of karst flora (Chen et al., 2012). For example, the Youjiang Basin, which mainly consists of broad non-karst terrains (Lu et al., 2006), is located at the midpoint between the northern and southern populations of X. vietnamensis (Figure 1). The Youjiang Basin and other non-karst areas between northern and southern population of X. vietnamensis might have acted as genetic barriers and resulted in isolated and fragmented populations, and restricted gene flow and migration between the northern and southern populations of X. vietnamensis.

Generally, bottleneck effects are found in populations with reduced population size due to natural catastrophes, habitat loss, alteration and fragmentation. As such, it is likely a historical climate event in combination with the fragmented habitat in this karst landscape may have led to the significant bottleneck detected in the X. vietnamensis populations. Meanwhile, in the context of demographic bottleneck, the isolation and fragmentation could have serious negative impact on the X. vietnamensis population due to random drift and inbreeding, and may have promoted genetic differentiation among populations (Nei et al., 1975; Sękiewicz et al., 2015).

Variation in Genome Size and Asymmetric Gene Flow

Our genome size data showed that X. vietnamensis is mixed-ploidy and populations in Guangxi possess both diploid and tetraploid cytotypes. The average tetraploid genome size of 48.02 pg/2C was similar to but slightly larger than previous study (44.60 pg/2C) using another internal standard and nuclei isolation buffers (Farhat et al., 2021); the average diploid genome size of 26.08 pg/2C is similar to that of diploid Juniperus species (Farhat et al., 2019). Although only four representative individuals per population were sampled from two populations each from northern and southern population groups, we found that all eight individuals from northern populations are diploids and these from southern populations are tetraploids.

While there was significant difference in genome size between the northern (diploid) and southern (tetraploid) populations, microsatellite diversity varied little between them. These differences may reflect the recent origin of tetraploid from the diploid (Lumaret and Barrientos, 1990; Ickert-Bond et al., 2020). However, these two cytotypes might have distinctly different genetic structure (Figures 3, 4), which was probably due to habitat differences and spatial isolation (Laport et al., 2016). Tetraploid populations appear to have greater negative inbreeding coefficients (FIS) (Table 4). We tested the impact of small population size on FIS (Supplementary Table S2), and found a trend of negative FIS with greater absolute values when sample size is small, but smaller size did not cause a shift of FIS from positive value to negative value or the other way round. These results suggest seedling production by selfing in tetraploid populations of X. vietnamensis. As reported in previous studies, chromosome doubling can lead to a breakdown of self-incompatibility (Soltis and Soltis, 2000; Sutherland et al., 2018). Thus, tetraploid populations may be more likely to establish after expansion or dispersal than diploid populations. As far as we know, many more tetraploid individuals and populations were found in the neighboring areas——Vietnam (Averyanov et al., 2013; Farhat et al., 2021). Our data revealed historical gene flow from north (diploid population) to south (tetraploid population) was higher than the reverse (Table 6). It is likely that tetraploid X.vietnamensis in southern population may be of autopolyploid origin and diploids in the northern populations may be the source populations, yet these hypotheses need to be further tested.

Conservation Implications

There is clear genetic and ploidy level distinction between the north and south populations in southwestern China according to the STRUCTURE analysis and genome size analysis. The disjunct geography and topography of the karst mountains and over 300 km of geographical distance between the northern and southern populations may have acted as barriers to gene flow. Hence the northern and southern populations should be treated as two different management units. Populations of X. vietnamensis are isolated as their habitat is confined to the mountain peaks. To reduce inbreeding and minimize bottleneck effect, artificial pollination or transplanting among fragmented populations in each unit should be implemented. Considering the rarity of wild individuals at present, we suggest in situ artificial regeneration programmes immediately for the populations, and urgent trials of ex situ plantations in Guangxi, China, through the collection, germination, cultivation of seeds and twig cuttage, similar to the strategy that has proven successful in Vietnam for this species.

In our study, sampled populations were restricted to provincial or national borders, remote from the human residential belt. The regions between the northern and southern populations are substantially impacted by humans (Zeng et al., 2007; Wang, 2011; Jiang et al., 2014). These imply that human activities led to the loss of habitats and the extremely small population size of X. vietnamensis. The northern populations are mostly located in the Guangxi Mulun National Nature Reserve, and the southern populations are located in the Guangxi Laohutiao Provincial Nature Reserve. In general, management effectiveness of nature reserves in China are relatively good, especially those with higher management level; but there are still some problems of nature reserves in China, such as the lacking information of boundaries and tenures, the poorly organized institution, the lacking of staff, fund and so on (Wang and Li, 2021). The Laohutiao Provincial Nature Reserve stretches 69 km along the border of China and Vietnam. Generally, it is not easy to effectively protect the ecology and biodiversity in the national borders (Wang and Li, 2021). Unfortunately, the distribution area of the southern populations of X. vietnamensis was accessible for agricultural exploitation, as we saw during the field survey. We recommend more attention and tighter management for the conservation of forest trees in this reserve.

Data Availability Statement

The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: GenBank, MZ514645-MZ514664; Dryad doi:10.5061/dryad.qnk98sfh7.

Author Contributions

KM and YL designed the study. YJ, WT, and YH performed the field work. TJ, YJ and JL analyzed the data. YJ and TJ wrote the articles. LEN revised the articles. All authors discussed the results and participated in the revision of the articles.

Funding

This work is supported by the National Science Foundation of China (Grant Nos. 41661012, 31622015) and the Guangxi Key Laboratory Construction Project (No. 19-185-7).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

We are grateful to the following colleagues for their assistance with field survey and sample collection: Ying Qin, Zhangping Huang, Guangfu Mou, Shichang Dai, Xitao Li, He Wang, Shanxiao Ou, Zhiqiang Yang, Huizhe Feng.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fgene.2021.733576/full#supplementary-material

References

Aguilar, R., Quesada, M., Ashworth, L., Herrerias-Diego, Y., and Lobo, J. (2008). Genetic Consequences of Habitat Fragmentation in Plant Populations: Susceptible Signals in Plant Traits and Methodological Approaches. Mol. Ecol. 17 (24), 5177–5188. doi:10.1111/j.1365-294x.2008.03971.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Averyanov, L. V., Hiep, N. T., Harder, D. K., and Loc, P. K. (2002). The History of Discovery and Natural Habitats of Xanthocyparis vietnamensis (Cupressaceae). Turczaninowia 5 (4), 31–39.

Google Scholar

Averyanov, L. V., Hiep, N. T., Khang, N. S., Tuan, L. M., The, P. V., Cuong, D. V., et al. (2013). Assessment of Xanthocyparis vietnamensis Nature Protected Status in Tuyen Quang Province. Rufford Small Grant Nat. Conservation Report 12585.

Google Scholar

Beerli, P. (2006). Comparison of Bayesian and Maximum-Likelihood Inference of Population Genetic Parameters. Bioinformatics 22, 341–345. doi:10.1093/bioinformatics/bti803

PubMed Abstract | CrossRef Full Text | Google Scholar

Bourge, M., Brown, S. C., and Siljak-Yakovlev, S. (2018). Flow Cytometry as Tool in Plant Sciences, With Emphasis on Genome Size and Ploidy Level Assessment. GenApp 2, 1. doi:10.31383/ga.vol2iss2pp1-12

CrossRef Full Text | Google Scholar

Bruford, M. W., Davies, N., Dulloo, M. E., Faith, D. P., and Walters, M. (2017). “Monitoring Changes in Genetic Diversity,” in The GEO Handbook on Biodiversity Observation Networks. Editors M. Walters, and R. J. Scholes (Cham: Springer International Publishing), 107–128. doi:10.1007/978-3-319-27288-7_5

CrossRef Full Text | Google Scholar

Chen, H., Zhang, W., Wang, K., and Hou, Y. (2012). Soil Organic Carbon and Total Nitrogen as Affected by Land Use Types in Karst and Non-Karst Areas of Northwest Guangxi, China. J. Sci. Food Agric. 92 (5), 1086–1093. doi:10.1002/jsfa.4591

CrossRef Full Text | Google Scholar

Christenhusz, M. J. M., Reveal, J. L., Farjon, A., Gardner, M. F., Mill, R. R., and Chase, M. W. (2011). A New Classification and Linear Sequence of Extant Gymnosperms. Phytotaxa 19 (1), 55–70. doi:10.11646/phytotaxa.19.1.3

CrossRef Full Text | Google Scholar

Chung, M. Y., Son, S., Herrando‐Moraira, S., Tang, C. Q., Maki, M., Kim, Y. D., et al. (2020). Incorporating Differences Between Genetic Diversity Of Trees and Herbaceous Plants in Conservation Strategies. Conserv. Biol. 34 (5), 1142–1151. doi:10.1111/cobi.13467

PubMed Abstract | CrossRef Full Text | Google Scholar

Dieringer, D., and Schlötterer, C. (2003). Microsatellite Analyser: A Platform Independent Analysis Tool for Large Microsatellite Data Sets. Mol. Ecol. Notes 3, 167–169.

CrossRef Full Text | Google Scholar

Doyle, J. J. T., and Doyle, J. L. (1990). Isolation of Plant DNA from Fresh Tissue. Focus 12, 13–15.

Google Scholar

Earl, D. A., and vonHoldt, B. M. (2012). Structure Harvester: A Website and Program for Visualizing Structure Output and Implementing the Evanno Method. Conserv. Genet. Resour. 4, 359–361. doi:10.1007/s12686-011-9548-7

CrossRef Full Text | Google Scholar

Edmands, S. (2007). Between a Rock and a Hard Place: Evaluating the Relative Risks of Inbreeding and Outbreeding for Conservation and Management. Mol. Ecol. 16, 463–475. doi:10.1111/j.1365-294X.2006.03148.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Evanno, G., Regnaut, S., and Goudet, J. (2005). Detecting the Number of Clusters of Individuals Using the Software Structure: A Simulation Study. Mol. Ecol. 14, 2611–2620. doi:10.1111/j.1365-294x.2005.02553.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Excoffier, L., Smouse, P. E., and Quattro, J. M. (1992). Analysis of Molecular Variance Inferred From Metric Distances Among DNA Haplotypes: Application to Human Mitochondrial DNA Restriction Data. Genetics 131, 479–491. doi:10.1093/genetics/131.2.479

PubMed Abstract | CrossRef Full Text | Google Scholar

Farhat, P., Hidalgo, O., Robert, T., Siljak-Yakovlev, S., Leitch, I. J., Adams, R. P., et al. (2019). Polyploidy in the Conifer Genus Juniperus: An Unexpectedly High Rate. Front. Plant Sci. 10 (676), 676. doi:10.3389/fpls.2019.00676

PubMed Abstract | CrossRef Full Text | Google Scholar

Farhat, P., Siljak-Yakovlev, S., Hidalgo, O., Rushforth, K., Bartel, J. A., Valentin, N., et al. (2021). Polyploidy in Cupressaceae: Discovery of a New Naturally Occurring Tetraploid, Xanthocyparis vietnamensis. J. Syst. Evol. [Epub ahead of print]. doi:10.1111/jse.12751

CrossRef Full Text | Google Scholar

Farjon, A., Hiep, N. T., Harder, D. K., Loc, P. K., and Averyanov, L. (2002). A New Genus and Species in Cupressaceae (Coniferales) from Northern Vietnam, Xanthocyparis vietnamensis. Novon 12 (2), 179–189. doi:10.2307/3392953

CrossRef Full Text | Google Scholar

Foll, M., and Gaggiotti, O. (2008). A Genome-Scan Method to Identify Selected Loci Appropriate for Both Dominant and Codominant Markers: A Bayesian Perspective. Genetics 180 (2), 977–993. doi:10.1534/genetics.108.092221

PubMed Abstract | CrossRef Full Text | Google Scholar

Galbraith, D. W., Harkins, K. R., Maddox, J. M., Ayres, N. M., Sharma, D. P., and Firoozabady, E. (1983). Rapid Flow Cytometric Analysis of the Cell Cycle in Intact Plant Tissues. Science 220 (4601), 1049–1051. doi:10.1126/science.220.4601.1049

PubMed Abstract | CrossRef Full Text | Google Scholar

Garza, J. C., and Williamson, E. G. (2001). Detection of Reduction in Population Size Using Data From Microsatellite Loci. Mol. Ecol. 10, 305–318. doi:10.1046/j.1365-294x.2001.01190.x

PubMed Abstract | CrossRef Full Text | Google Scholar

González-Martínez, S. C., Dubreuil, M., Riba, M., Vendramin, G. G., Sebastiani, F., and Mayol, M. (2010). Spatial Genetic Structure of Taxus baccata L. in the Western Mediterranean Basin: Past and Present Limits to Gene Movement Over a Broad Geographic Scale. Mol. Phylogenet. Evol. 55 (3), 805–815. doi:10.1016/j.ympev.2010.03.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Grabherr, M. G., Haas, B. J., Yassour, M., Levin, J. Z., Thompson, D. A., Amit, I., et al. (2011). Full-Length Transcriptome Assembly from Rna-Seq Data Without a Reference Genome. Nat. Biotechnol. 29 (7), 644–652. doi:10.1038/nbt.1883

PubMed Abstract | CrossRef Full Text | Google Scholar

Groves, C. (2003). Drafting a Conservation Blueprint: A practitioner’s Guide to Planning for Biodiversity. Washington, DC: Island Press.

Google Scholar

Guo, Y., Xiang, W., Wang, B., Li, D., Mallik, A. U., Chen, H. Y. H., et al. (2018). Partitioning Beta Diversity in a Tropical Karst Seasonal Rainforest in Southern China. Sci. Rep. 8 (1), 17408. doi:10.1038/s41598-018-35410-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Gutiérrez, F., and Gutiérrez, M. (2016). “Karst Landforms,” in Landforms of the Earth: An Illustrated Guide. Editors F. Gutiérrez, and M. Gutiérrez (Cham: Springer International Publishing), 59–101.

Google Scholar

Hamilton, M. B. (2009). Population Genetics. Chichester: Wiley-Blackwell.

Google Scholar

Hamrick, J. L. (2004). Respnse of Forest Trees to Global Environmental Changes. For. Ecol. Manag. 197 (1-3), 323–335. doi:10.1016/j.foreco.2004.05.023

CrossRef Full Text | Google Scholar

Hewitt, G. (2000). The Genetic Legacy of the Quaternary Ice Ages. Nature 405 (6789), 907–913. doi:10.1038/35016000

PubMed Abstract | CrossRef Full Text | Google Scholar

Hizume, M., Kondo, T., Shibata, F., and Ishizuka, R. (2001). Flow Cytometric Determination of Genome Size in the Taxodiaceae, Cupressaceae sensu stricto and Sciadopityaceae. Cytologia 66 (3), 307–311. doi:10.1508/cytologia.66.307

CrossRef Full Text | Google Scholar

Hobohm, C. (2014). Endemism in Vascular Plants. Cham: Springer Netherlands.

Google Scholar

Ickert-Bond, S. M., Sousa, A., Min, Y., Loera, I., Metzgar, J., Pellicer, J., et al. (2020). Polyploidy in Gymnosperms - Insights into the Genomic and Evolutionary Consequences of Polyploidy in Ephedra. Mol. Phylogenet. Evol. 147, 106786. doi:10.1016/j.ympev.2020.106786

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiang, Y. L., Meng, T., Xu, W. B., Tan, W. N., Zhang, Q., and Liu, Y. (2021). Community Characteristics of Endangered Gymnosperms and Their Topographic Relationships in a Karst Mountaintop Region. Acta Ecol. Sin. 41 (5), 1868–1877. doi:10.5846/stxb201904020635

CrossRef Full Text | Google Scholar

Jiang, Z., Lian, Y., and Qin, X. (2014). Rocky Desertification in Southwest China: Impacts, Causes, and Restoration. Earth-Science Rev., 132. doi:10.1016/j.earscirev.2014.01.005

CrossRef Full Text | Google Scholar

Jombart, T. (2008). Adegenet: A R package for the Multivariate Analysis of Genetic Markers. Bioinformatics 24 (11), 1403–1405. doi:10.1093/bioinformatics/btn129

PubMed Abstract | CrossRef Full Text | Google Scholar

Jombart, T., Devillard, S., and Balloux, F. (2010). Discriminant Analysis of Principal Components: A New Method for the Analysis of Genetically Structured Populations. BMC Genet. 11 (1), 94. doi:10.1186/1471-2156-11-94

PubMed Abstract | CrossRef Full Text | Google Scholar

Jump, A. S., Mátyás, C., and Peñuelas, J. (2009). The Altitude-for-Latitude Disparity in the Range Retractions of Woody Species. Trends Ecol. Evol. 24, 694–701. doi:10.1016/j.tree.2009.06.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Kalinowski, S. T., Taper, M. L., and Marshall, T. C. (2007). Revising How the Computer Program Cervus Accommodates Genotyping Error Increases Success in Paternity Assignment. Mol. Ecol. 16, 1099–1106. doi:10.1111/j.1365-294x.2007.03089.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Laport, R. G., Minckley, R. L., and Ramsey, J. (2016). Ecological Distributions, Phenological Isolation, and Genetic Structure in Sympatric and Parapatric Populations of the Larrea tridentata Polyploid Complex. Am. J. Bot. 103 (7), 1358–1374. doi:10.3732/ajb.1600105

CrossRef Full Text | Google Scholar

Li, J., Milne, R. I., Ru, D., Miao, J., Tao, W., Zhang, L., et al. (2020). Allopatric Divergence and Hybridization Within Cupressus chengiana (Cupressaceae), a Threatened Conifer in the Northern Hengduan Mountains of Western China. Mol. Ecol. 29 (7), 1250–1266. doi:10.1111/mec.15407

PubMed Abstract | CrossRef Full Text | Google Scholar

Liao, S., Cui, K., Tian, B., Zhang, Z., Liu, A., Li, K., et al. (2015). The Effect of Long-Term Historical Habitat Fragmentation on Genetic Diversity of the Relictual Conifer Calocedrus macrolepis (Cupressaceae) in China. Braz. J. Bot. 38 (3), 567–577. doi:10.1007/s40415-015-0168-4

CrossRef Full Text | Google Scholar

Little, D. P. (2006). Evolution and Circumscription of the True Cypresses (Cupressaceae: Cupressus). Syst. Bot. 31, 461–480. doi:10.1600/036364406778388638

CrossRef Full Text | Google Scholar

Little, D. P., Schwarzbach, A. E., Adams, R. P., and Hsieh, C. F. (2004). The Circumscription and Phylogenetic Relationships of Callitropsis and the Newly Described Genus Xanthocyparis (Cupressaceae). Am. J. Bot. 91, 1872–1881. doi:10.3732/ajb.91.11.1872

PubMed Abstract | CrossRef Full Text | Google Scholar

Lu, G., Hu, G., Zhang, N., Zhang, G., Pan, Y., and Peng, Y. (2006). Recent Approach to Space-Time Distribution and Sedimentary Structural Evolution of Permian Reef in Youjiang Basin. Geol. Rev. 52 (2), 190–197.

Google Scholar

Lumaret, R., and Barrientos, E. (1990). Phylogenetic Relationships and Gene Flow Between Sympatric Diploid and Tetraploid Plants of Dactylis glomerata (Gramineae). Pl. Syst. Evol. 169, 81–96. doi:10.1007/bf00935987

CrossRef Full Text | Google Scholar

Manni, F., Guérard, E., and Heyer, E. (2004). Geographic Patterns of (Genetic, Morphologic, Linguistic) Variation: How Barriers can be Detected by Using Monmonier’s Algorithm. Hum. Biol. 76, 173–190. doi:10.1353/hub.2004.0034

PubMed Abstract | CrossRef Full Text | Google Scholar

Mao, K., Hao, G., Liu, J., Adams, R. P., and Milne, R. I. (2010). Diversification and Biogeography of Juniperus (Cupressaceae): Variable Diversification Rates and Multiple Intercontinental Dispersals. New Phytol. 188 (1), 254–272. doi:10.1111/j.1469-8137.2010.03351.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Mao, K., Ruhsam, M., Ma, Y., Graham, S. W., Liu, J., Thomas, P., et al. (2019). A Transcriptome-Based Resolution for a Key Taxonomic Controversy in Cupressaceae. Ann. Bot. 123 (1), 153–167. doi:10.1093/aob/mcy152

PubMed Abstract | CrossRef Full Text | Google Scholar

Meng, T., Peng, R. C., Zhong, G. F., You, Z. J., Tan, W. N., and Xu, W. B. (2013). Xanthocyparis Farjon & Hiep, A newly Recorded Genus of Cupressaceae from China. Guihaia 33 (3), 388–391.

Google Scholar

Nei, M., Maruyama, T., and Chakraborty, R. (1975). The Bottleneck Effect and Genetic Variability in Populations. Evolution 29, 1–10. doi:10.1111/j.1558-5646.1975.tb00807.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Nybom, H. (2004). Comparison of Different Nuclear DNA Markers for Estimating Intraspecific Genetic Diversity in Plants. Mol. Ecol. 13, 1143–1155. doi:10.1111/j.1365-294x.2004.02141.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Peakall, R., and Smouse, P. E. (2012). GenAlEx 6.5: Genetic Analysis in Excel. Population Genetic Software for Teaching and Research--An Update. Bioinformatics 28, 2537–2539. doi:10.1093/bioinformatics/bts460

PubMed Abstract | CrossRef Full Text | Google Scholar

Pritchard, J. K., Stephens, M., and Donnelly, P. (2000). Inference of Population Structure Using Multilocus Genotype Data. Genetics 155, 945–959. doi:10.1093/genetics/155.2.945

PubMed Abstract | CrossRef Full Text | Google Scholar

Reed, D. H., and Frankham, R. (2003). Correlation Between Fitness and Genetic Diversity. Conserv. Biol. 17 (1), 230–237. doi:10.1046/j.1523-1739.2003.01236.x

CrossRef Full Text | Google Scholar

Rice, W. (1989). Analyzing Tables of Statistical Tests. Evol. Int. J. Org. Evol. 43, 223–225.

CrossRef Full Text | Google Scholar

Rousset, F. (2008). Genepop’007: A Complete Re-Implementation of the Genepop Software for Windows and Linux. Mol. Ecol. Resour. 8, 103–106. doi:10.1111/j.1471-8286.2007.01931.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Rozen, S., and Skaletsky, H. (2000). “Primer3 on the WWW for General Users and for Biologist Programmers,” in Bioinformatics Methods and Protocols. Editors S. Misener, and S. A. Krawetz (Totowa, NJ: Humana Press), 365–386.

PubMed Abstract | CrossRef Full Text | Google Scholar

Sękiewicz, K., Dering, M., Sękiewicz, M., Boratyńska, K., Iszkuło, G., Litkowiec, M., et al. (2015). Effect of Geographic Range Discontinuity on Species Differentiation—East-Mediterranean Abies cilicica: A Case Study. Tree Genet. Genomes 11, 810.

Google Scholar

Slarkin, M. (1985). Gene Flow in Natural Populations. Annu. Rev. Ecol. Syst. 16, 393–430. doi:10.1146/annurev.es.16.110185.002141

CrossRef Full Text | Google Scholar

Soltis, P. S., and Soltis, D. E. (2000). The Role of Genetic and Genomic Attributes in the Success of Polyploids. Proc. Natl. Acad. Sci. 97 (13), 7051–7057. doi:10.1073/pnas.97.13.7051

PubMed Abstract | CrossRef Full Text | Google Scholar

Su, Y., Tang, Q., Mo, F., and Xue, Y. (2017). Karst Tiankengs as Refugia for Indigenous Tree Flora Amidst a Degraded Landscape in Southwestern China. Sci. Rep. 7, 4249. doi:10.1038/s41598-017-04592-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Sutherland, B. L., Quarles, B. M., and Galloway, L. F. (2018). Intercontinental Dispersal and Whole‐Genome Duplication Contribute to Loss of Self‐Incompatibility in a Polyploid Complex. Am. J. Bot. 105 (2), 249–256. doi:10.1002/ajb2.1027

CrossRef Full Text | Google Scholar

Tang, C. Q. (2015). “Endemism and Tertiary Relict Forests,” in The Subtropical Vegetation of Southwestern China: Plant Distribution, Diversity and Ecology. Editor C. Q. Tang (Dordrecht: Springer Netherlands), 185–273. doi:10.1007/978-94-017-9741-2_7

CrossRef Full Text | Google Scholar

Tang, C. Q., Matsui, T., Ohashi, H., Dong, Y.-F., Momohara, A., Herrando-Moraira, S., et al. (2018). Identifying Long-Term Stable Refugia for Relict Plant Species in East Asia. Nat. Commun. 9 (1), 4488. doi:10.1038/s41467-018-06837-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Tang, S., Dai, W., Li, M., Zhang, Y., Geng, Y., Wang, L., et al. (2008). Genetic Diversity of Relictual and Endangered Plant Abies ziyuanensis (Pinaceae) Revealed by AFLP and SSR Markers. Genetica 133, 21–30. doi:10.1007/s10709-007-9178-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Thiel, T., Michalek, W., Varshney, R., and Graner, A. (2003). Exploiting EST Databases for the Development and Characterization of Gene-Derived SSR-Markers in Barley (Hordeum vulgare L.). Theor. Appl. Genet. 106 (3), 411–422. doi:10.1007/s00122-002-1031-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Thomas, P. (2013). Xanthocyparis vietnamensis. The IUCN Red List of Threatened Species, e.T44028A2991576. doi:10.2305/IUCN.UK.2013-1.RLTS.T44028A2991576.en

CrossRef Full Text | Google Scholar

Tian, S., Luo, L.-C., Ge, S., and Zhang, Z.-Y. (2008). Clear Genetic Structure of Pinus kwangtungensis (Pinaceae) Revealed by a Plastid DNA Fragment with a Novel Minisatellite. Ann. Bot. 102, 69–78. doi:10.1093/aob/mcn068

PubMed Abstract | CrossRef Full Text | Google Scholar

Untergasser, A., Cutcutache, I., Koressaar, T., Ye, J., Faircloth, B. C., Remm, M., et al. (2012). Primer3-New Capabilities and Interfaces. Nucleic Acids Res. 40 (15), e115. doi:10.1093/nar/gks596

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, W., and Delang, C. O. (2011). Chinese Forest Policies in the Age of Ideology (1949-1977). Int. For. Rev. 13, 416–430. doi:10.1505/146554811798811290

CrossRef Full Text | Google Scholar

Wang, W., and Li, J. (2021). In-Situ Conservation of Biodiversity in China: Advances and Prospects. Biodiv. Sci. 29 (2), 133–149. doi:10.17520/biods.2020070

CrossRef Full Text | Google Scholar

Wang, Z.-S., Sun, H.-Q., Wang, H.-W., and Ge, S. (2010). Isolation and Characterization of 50 Nuclear Microsatellite Markers for Cathaya argyrophylla, a Chinese Endemic Conifer. Am. J. Bot. 97, e117–e120. doi:10.3732/ajb.1000270

PubMed Abstract | CrossRef Full Text | Google Scholar

Weeks, A. R., Sgro, C. M., Young, A. G., Frankham, R., Mitchell, N. J., Miller, K. A., et al. (2011). Assessing the Benefits and Risks of Translocations in Changing Environments: A Genetic Perspective. Evol. Appl. 4, 709–725. doi:10.1111/j.1752-4571.2011.00192.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Wright, S. (1978). “Evolution and the Genetics of Populations,” in Variability within and Among Natural Populations. Chicago: Bibliovault OAI Repository, the University of Chicago Press.

Google Scholar

Wu, X., Ruhsam, M., Wen, Y., Thomas, P. I., Worth, J. R. P., Lin, X., et al. (2020). The Last Primary Forests of the Tertiary Relict Glyptostrobus pensilis Contain the Highest Genetic Diversity. For. Int. J. For. Res. 93 (3), 359–375. doi:10.1093/forestry/cpz063

CrossRef Full Text | Google Scholar

Yamamoto, M., Kurata, K., and Setoguchi, H. (2017). Conservation Genetics of an ex situ population of Primula reinii var. rhodotricha, an Endangered Primrose Endemic to Japan on a Limestone Mountain. Conserv Genet. 18 (5), 1141–1150. doi:10.1007/s10592-017-0966-2

CrossRef Full Text | Google Scholar

Yin, Q., Chen, S., Guo, W., Huang, Y., Huang, Y., Zhou, R., et al. (2018). Pronounced Genetic Differentiation in Fokienia hodginsii Revealed by Simple Sequence Repeat Markers. Ecol. Evol. 8 (22), 10938–10951. doi:10.1002/ece3.4560

PubMed Abstract | CrossRef Full Text | Google Scholar

Yin, Q. Y., Fan, Q., Li, P., Truong, D., Zhao, W. Y., Zhou, R. C., et al. (2021). Neogene and Quaternary Climate Changes Shaped the Lineage Differentiation and Demographic History of Fokienia hodginsii (Cupressaceae s.l.), a Tertiary Relict in East Asia. J. Syst. Evol. 59 (5), 1081–1099.

CrossRef Full Text | Google Scholar

Zeng, F., Peng, W., Song, T., Wang, K., Wu, H., Song, X., et al. (2007). Changes in Vegetation After 22 years’ Natural Restoration in the Karst Disturbed Area in Northwestern Guangxi, China. Acta Ecol. Sin. 27 (12), 5110–5119. doi:10.1016/s1872-2032(08)60016-5

CrossRef Full Text | Google Scholar

Zhang, Y., Wang, B., Qi, S., Dong, M., Wang, Z., Li, Y., et al. (2019). Ploidy and Hybridity Effects on Leaf Size, Cell Size and Related Genes Expression in Triploids, Diploids and Their Parents in Populus. Planta 249 (3), 635–646. doi:10.1007/s00425-018-3029-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Zonneveld, B. J. M. (2012). Conifer Genome Sizes of 172 Species, Covering 64 of 67 Genera, Range from 8 to 72 Picogram. Nordic J. Bot. 30 (4), 490–502. doi:10.1111/j.1756-1051.2012.01516.x

CrossRef Full Text | Google Scholar

Keywords: karst, Cupressaceae, microsatellites, flow cytometry, ploidy level, conservation genetics

Citation: Jiang Y, Ju T, Neaves LE, Li J, Tan W, Huang Y, Liu Y and Mao K (2021) Distinct Genetic Structure Reflects Ploidy Level Differentiation in Newly Discovered, Extremely Small Populations of Xanthocyparis vietnamensis from Southwestern China. Front. Genet. 12:733576. doi: 10.3389/fgene.2021.733576

Received: 30 June 2021; Accepted: 15 September 2021;
Published: 01 November 2021.

Edited by:

Renchao Zhou, Sun Yat-sen University, China

Reviewed by:

Yuchen Yang, University of North Carolina at Chapel Hill, United States
Wei Wu, Zhongkai University of Agriculture and Engineering, China

Copyright © 2021 Jiang, Ju, Neaves, Li, Tan, Huang, Liu and Mao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yan Liu, Z3hpYmx5QDE2My5jb20=; Kangshan Mao, bWFva2FuZ3NoYW5AMTYzLmNvbQ==, bWFva2FuZ3NoYW5Ac2N1LmVkdS5jbg==

These authors have contributed equally to this work

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