Skip to main content
Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Molecular phylogeny and diversification timing of the Nemouridae family (Insecta, Plecoptera) in the Japanese Archipelago

  • Maribet Gamboa ,

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Software, Visualization, Writing – original draft, Writing – review & editing

    Affiliation Department of Civil and Environmental Engineering, Ehime University, Matsuyama, Japan

  • David Muranyi,

    Roles Funding acquisition, Investigation, Methodology, Writing – review & editing

    Affiliations Department of Civil and Environmental Engineering, Ehime University, Matsuyama, Japan, Deparment of Zoology, Plant Protection Institute Centre for Agricultural Research, Hungarian Academy of Sciences, Budapest, Hungary

  • Shota Kanmori,

    Roles Data curation, Formal analysis, Methodology

    Affiliation Department of Civil and Environmental Engineering, Ehime University, Matsuyama, Japan

  • Kozo Watanabe

    Roles Writing – review & editing

    Affiliation Department of Civil and Environmental Engineering, Ehime University, Matsuyama, Japan


The generation of the high species diversity of insects in Japan was profoundly influenced by the formation of the Japanese Archipelago. We explored the species diversification and biogeographical history of the Nemouridae Billberg, 1820 family in the Japanese Archipelago using mitochondrial DNA and nuclear DNA markers. We collected 49 species among four genera: Indonemoura Baumann, 1975; Protonemura Kempny, 1898; Amphinemura, Ris 1902 and Nemoura Latreille, 1796 in Japan, China, South Korea and North America. We estimated their divergence times—based on three molecular clock node calibrations—using Bayesian phylogeography approaches. Our results suggested that Japanese Archipelago formation events resulted in diversification events in the middle of the Cretaceous (<120 Ma), speciation in the Paleogene (<50 Ma) and intra-species diversification segregated into eastern and western Japan of the Fossa Magna region at late Neogene (20 Ma). The Indonemoura samples were genetically separated into two clades—that of Mainland China and that of Japan. The Japanese clade clustered with the Nemouridae species from North America, suggesting the possibility of a colonisation event prior to the formation of the Japanese Archipelago. We believe that our results enhanced the understanding both of the origin of the species and of local species distribution in the Japanese Archipelago.


The East Asian region—and in particular, the Japanese Archipelago—is considered to have high insect biodiversity [1], [2]. The high degree of Japanese insect biodiversity is a result of several mechanisms—in particular, the complex geological history. The Japanese Archipelago originated in the middle of the Miocene [3] as an independent formation of eastern and western Japanese landmasses. Extensive geographical changes and large-scale climatic changes throughout the islands facilitated the subsequent connection and disconnection of Japanese landmasses from the Eurasian continent, and the formation of tectonic lines (as the median tectonic line, MTL; and the Itoigawa-Shizuoka tectonic line, ISLT) [3], [4], [5]. These geological events—facilitating for the colonisation of insects from the continent and their subsequent diversification as endemic lineages (i.e. new species)—substantially contributed to the high diversity of insects in Japan [2].

The process of species diversification has been intensively explored through phylogeographical approaches [6], [7]. These approaches have allowed for the observation of the historical process responsible for the current geographical distribution of individuals [6]. Molecular approaches to phylogeographic studies, using specific genes—such as mitochondrial DNA (mtDNA) or nuclear DNA (nDNA)—allow for a better understanding of species diversity by resolving complex taxonomic groups of species (for instance, cryptic species and species groups) [7]. Molecular phylogeography has provided valuable insights into the historical process of Japanese Archipelago formation underlying insect diversification. Previous studies identified genetic differentiation within species between the Japanese landmasses and the Eurasian continent (for instance, the mayflies Isonychia japonica (Ulmer, 1919) [8]; caddisflies Palaeagapetus spp. (Ulmer, 1912) [9] and beetles Ohomopterus spp. (Nakane, 1953) [10] and the Carabina subtribe [11]). Dispersal events via land bridges (islands between continents) from the Eurasian continent to the Japanese Archipelago (of, for instance, the orthopteran Locusta migratoria Linnaeus, 1758, [12]; mayflies Ephron spp. (Williamson, 1802), [13]) or, in reverse, from the Japanese Archipelago to the Eurasian continent (of, for instance, water bugs Appasus spp. Amyot and Serville, 1843, [14]) were additionally identified before, during and after the formation of the Japan Archipelago.

Aquatic insects have advantages in the studies of phylogeography, as their specialised ecological requirements and habitat range make aquatic insect species susceptible to geological changes. Among the Plecoptera order [15], the family Nemouridae is one of the largest and most dominant aquatic insect groups. The family comprises 20 genera and more than 400 species distributed throughout the Northern Hemisphere and across the equator in the Sunda Archipelago [16]. Several genera of the Nemouridae family have distinct disjunctions in their distribution [15]. For example, Ostrocerca Ricker, 1952, Prostoia Ricker, 1952 and Soyedina Ricker, 1952 were found in both the extreme western and the extreme eastern regions of North America, but they were absent in the central area [17], [18]. Similar disjunctive distributions were also observed among Protonemura, Indonemoura, Sphaeronemoura Shimizu & Sivec, 2001, and Illiesonemoura Baumann, 1975 in the Palaearctic region [19], the western and eastern Himalayan ranges [20] and North and South India [15]. Podmosta Ricker, 1952 and Zapada Ricker, 1952 (Nemourinae Billberg, 1820) are two interesting cases distributed across the Nearctic region and East Asia [21], [22]. Previous studies have suggested that their current habitat distribution could be associated with mountain formation and land bridges. In Japan, the Nemouridae family is widely distributed with four genera [23]—Indonemoura; Protonemura; Amphinemura; and Nemoura. To date, 30 Nemoura species, 17 Amphinemura species, 12 Protonemura species and 1 Indonemoura species have been reported in Japan [16]. However, their evolutionary history in the Japanese Archipelago remains unknown.

We studied the molecular phylogeny of the aquatic insect Nemouridae (Plecoptera) in the Japanese Archipelago with comprehensive genera-level sampling using mitochondrial cytochrome c oxidase 1 (cox1) and nuclear histone 3 (H3) markers. We hypothesised that the Nemouridae family diversification could be linked to the geological formation of the Japanese Archipelago. Therefore, we estimated the phylogenetic relationships among Nemouridae species and genera with reference to their historical biogeography. We focused on geographic events of Japanese Archipelago formation and their influence on the divergence time among the genera and species using a combination of fossil records and the Archipelago formation history. Furthermore, to estimate the historical process of the phylogeography of Nemouridae in Japan, we compared the phylogenetic relationships among the specimens from South Korea, China and North America, that are assumed to be the potential sources of Japanese Nemouridae because of the geological formation history of the Japanese Archipelago.

Material and methods

Study sites and sample collection

Our sampling sites in Japan comprised 32 sampling sites on Hokkaido Island, 83 on Honshu Island and 27 on Shikoku Island. The field sampling was conducted without the necessity of any special permit. None of the Nemouridae species was found on Hokkaido Island during sampling. All species reported from Hokkaido are known to occur on either Honshu or Shikoku Islands. Herein, we only reported on the sampling sites wherein specimens were found. We collected 20, 7, 8 and 1 species of the genera Nemoura, Amphinemura, Protonemura and Indonemoura, respectively, on 110 sampling sites in Japan (Fig 1, S1 Table). Additionally, 14 species collected from 8 sampling sites of Mainland China and 2 of South Korea (S1 Table, Fig 2) and 100 specimens of the three species Zapada columbiana (Claassen, 1923), Z. cinctipes (Banks, 1897), and Podmosta delicatula (Claassen, 1923) of subfamily Nemourinae collected from 15 sampling sites of North America (western United States of America and Alaska) were included in our analysis. We added these samples from outside of Japan because of their geographical proximity to the Japanese Archipelago and their geological formation histories. The maps were prepared in QGIS software v 2.18 under the GNU free Documentation License.

Fig 1. The Japanese islands and distribution of 110 sampling sites from where Nemouridae samples were collected (open circles).

The map was prepared using QGIS v 2.18 under the GNU free documentation License with political boundaries from the Global Database of Administrative Areas (

Fig 2. Concatenated Bayesian phylogeny (cox1 + H3) of the East Asian Nemouridae family.

The phylogenetic tree nodes were calibrated using 180 Ma based on fossil records + 15 to 30 Ma based on the Japanese Archipelago formation. Calibration and geological time are shown at the bottom of the tree. A 95% HPD is indicated as a horizontal grey bar and posterior probabilities are shown for each node. Circle symbol () in the nodes indicates intra-species diversification based on the eastern and western Japanese boundaries of the Fossa Magna region. Inserted upper map shows sample site locations for Japan (black), China (red) and South Korea (blue) as dots. Colour branches indicate sample location distribution as shown in the map. The map was prepared using QGIS v 2.18 under the GNU free documentation License with political boundaries from the Global Database of Administrative Areas (

We collected adult insects using hand nets around riversides. We stored samples in 80% ethanol in the field, and replaced the ethanol with fresh 99.5% ethanol after morphological identification. We identified individuals according to the taxonomical keys of [21], [23], [24], [25], [26], [27], [28], [29], [30], [31] and [32]. Undescribed species in our study were morphologically sorted based on our taxonomic expertise and inconclusive taxonomic keys.

DNA extraction, amplification and sequencing

We genetically analysed a total of 289 individuals, out of which 189 were from East Asia (males, 97; females, 92) and 100 were from North America (males, 92; females, 8). We extracted genomic DNA individually using DNeasy tissue kits (Qiagen GmbH, Hilden, Germany), following the manufacturer’s instructions. We amplified a 658-bp fragment of mtDNA cox1 using LCO-1490 and HCO-2198 primers [33] with an annealing temperature of 38°C and 40 PCR cycles. Further, we amplified a 328-bp fragment of nDNA marker histone 3 (H3) using the universal primers H3F and H3R [34] with an annealing temperature of 58°C and 40 PCR cycles. We purified the PCR products using the QIAquick PCR Purification Kit (Qiagen GmbH, Hilden, Germany) and sequenced them in both directions using the same primers as mentioned above. Cox1 and H3 sequences were sequenced by Eurofins Operon (Tokyo, Japan). All sequence data reported here have been deposited in GenBank (COI: MK132196-MK132472; H3: MK132473-MK132742).

Sequence analysis

We assembled and edited forward and reverse sequences using CodonCode Aligner v 3.5 (Codon Code Corporation, Dedham, USA). All sequences were aligned using ClustalW ( [35]. Alignment of H3 was based on the conservation of the amino acid reading frame across the data. Only a few nucleotide sites in the sequence showed heterozygous nucleotides (i.e. double peaks). These nucleotide sites were treated as unambiguous and they were omitted from our phylogenetic analysis. All alignment data have been deposited in Dryad repository.

We calculated the genetic diversity by the number of polymorphic sites, number of haplotypes and both mean nucleotide substitution rate (i.e. individuals within species) and pairwise nucleotide substitution rate (i.e. between species), with the Kimura 2-parameter model. We performed all analyses using DnaSp v5.10 [36]. All analyses were performed for cox1 and h3 separately.

All sequences of the mtDNA and nDNA markers were compared with the NCBI nucleotide database using blastn queries ( to corroborate species identification (DNA barcoding, similarity > 98%) and to discard possible sequence errors.

DNA species delimitation

To corroborate the morphological species identification match with our molecular data, we implemented a DNA species delimitation analysis. Putative DNA species were delineated using the General Mixed Yule Coalescent model (GMYC; [37]). An ultrametric gene tree of cox1 gene was constructed using BEST v1.8.3 [38], and the GMYC analysis was performed using the splits package [39] in R ver. 3.3 (R Core Team). We used a single version of the GMYC model. The maximum likelihood of the GMYC model was tested using the likelihood ratio test against a one-species null model (i.e. entire tree is considered as a single coalescent).

Molecular clock analysis

We estimated the evolutionary history of the family in the Japanese Archipelago according to the timing of the divergence of the lineages. For this estimation, we implemented a Bayesian phylogenetic analysis in combination with a molecular clock analysis using BEAST v.2.4.4 [40] with Zwicknia bifrons (Newman, 1838) (Capniidae Banks, 1990) as a outgroup for cox1 and H3 (own sequences) separately. This outgroup was selected owing to their close phylogenetic relationship with Nemouridae [41], [42]. To observe the divergence time, we adopted a relax clock model [43] following a log normal distribution, and calibrated the phylogenetic tree nodes using three types of molecular clock analysis. The first calibration was based on fossil records of the Nemouridae family [44]. We calibrated the nodes at 180 million years ago (Ma) and adjusted the parameters with a standard deviation of 20 Ma, as suggested in a previous study [45] for a 95% highest posterior density (HPD). For this analysis, we implemented a fossilised birth death model [46] for tree prior parameter. The second calibration was based on the Japanese Archipelago formation events dated from 15 to 30 Ma [3]. We applied several calibrations from 15, 20, 25 and 30 Ma at all nodes representing taxonomic species. All calibrations were adjusted to 5 Ma as a standard deviation for a 95% HPD and a fossilised birth death model [46] for tree prior parameter. Lastly, the third calibration was the time to the most recent common ancestor (TMRCA) to observe species diversification patterns based on the mean substitution rate of cox1. Using a Yule model tree prior parameter [47], we applied the substitution rate for insect cox1 of 1.5% [48] and 3.54% [49] per million years for a 95% HPD.

For all branch age calibrations (namely, fossil, biogeographic and mtDNA substitution rate), we performed MCMC for 50 million generations, and log dating trees (BEAST parameters) for every 5000 generations. We tested the output files for convergence after removing a 10% burn-in by examining the effective sampling size using Tracer v1.5 [50]. We pooled the four resulting output trees from biogeographical calibration analysis into a single tree. We then pooled the resulting single tree from biogeographical calibration and the single tree from fossil calibration analyses into a single tree. We performed all pooling analyses using Log Combiner v1.6.1 (BEAST package) summarised with Tree Annotator (BEAST package) and visualised using FigTree v1.3.1 [51]. We performed the analyses for cox1 and H3 separately. In summary, three molecular clock calibration trees were obtained, two for cox1 (fossil + biogeography and cox1 rates) and one for H3 (fossil + biogeography). The incongruence length difference test (ILD) [52] was conducted to test the congruence of tree topologies (fossil + biogeography) between cox1 and H3 using Tree Analysis Technology (TNT) [53]. ILD test revealed no significant differences in terms of the Bayesian tree topologies between cox1 and H3 (P = 0.8); therefore, both markers were polled into a single tree for further analysis. The tree files have been deposited in the Dryad repository.

Phylogenetic analysis between Nemoura from Japan and North America

To observe the phylogenetic relationship between Nemouridae from Japan and North America (Zapada columbiana, Z. cinctipes and Podmosta delicatula), we analysed the maximum likelihood (ML) phylogenetic trees of cox1 and H3 separately using PhyML 3.1 [54]. The General Time-Reversible (GTR) model and gamma distribution were selected for both markers (cox1 and H3) based on a separate test performed with jModel Test v.3 [55] and using Zwicknia bifrons (Capniidae) as an outgroup as described above. The trees were bootstrapped using 10,000 replications.


Genetic diversity and DNA phylogeny

For studying the phylogeny of Nemouridae in the Japanese Archipelago, we analysed two molecular markers. Cox1 sequences were of 658 bp length, with 247 polymorphic sites, 237 parsimony-informative sites, 10 singletons and a mean nucleotide substitution rate of 0.151. H3 sequences were of 328 bp length, with 67 polymorphic sites, 54 parsimony-informative sites, 13 singletons and a mean nucleotide substitution rate of 0.051. No gaps were detected for either cox1 or H3 sequences. In total, for cox1 and H3, we identified 128 and 68 haplotypes, respectively.

The log-likelihood of the GMYC model at the optimal threshold (111.02) was significantly better than the null model of a single coalescent (logL = 56.99) in the likelihood ratio test (p < 0.001). Most clades have GMYC-support values higher than 0.9, implying that the probability of the clades being delimited as separate GMYC-species among the alternative models of delimitation (within a 95% confidence set) is higher than 0.9. The single-threshold model delimited 61 putative species (S1 Table) (confidence interval: 58–65) composed of 39 clusters (confidence interval: 38–42), indicating that some of the inferred putative species were singletons (i.e. only one sequence). These results agreed with our 34 morphologically identified and 15 undescribed (five species of Protonemura, seven of Nemoura, one of Indonemoura and two of Amphinemura) species. Eight species (I. nohirae (Okamoto, 1922), A. decemseta Okamoto, 1922, A. zonata Okamoto, 1922, A. longispina Okamoto, 1922, A. megaloba (Kawai, 1960), N. uenoi Kawai, 1954, N. chinonis Okamoto, 1922, and N. cf. cercispinosa Kawai, 1960) showed two putative DNA-species. While A. decemseta showed multiple putative DNA-species (three putative DNA-species), N. sanbena Shimizu (1993) and P. kohnoae Shimizu, 1998, showed two putative DNA-species in the same sampling site suggesting the presence of cryptic species. The congruence of H3 phylogenetic groups provided confirmation of DNA-based groups detected by GMYC.

We observed the genetic diversity of the species per island (Table 1). Honshu had the highest number of species (26 species), haplotype richness (63) and mean nucleotide substitution rate (average 0.027). Five species were found throughout the three Japanese islands (Honshu, Shikoku and Kyushu), i.e. A. decemseta, A. zonata, N. cf. cercispinosa, N. chinonis and I. nohirae, with a mean nucleotide substitution rate ranging from 0.011 to 0.126 and a total of 23 haplotypes. N. sanbena haplotypes were observed in two different branches in the phylogenetic tree, both within N. cf. cercispinosa and as an isolated branch.

Table 1. Regional distribution of sample size (n), haplotype richness (h) and mean nucleotide substitution rate of Nemouridae species among the three main islands in Japan, based on mitochondrial DNA (cox1) sequences.

Total species richness was 26, 23 and 6 for Honshu, Shikoku and Kyushu, respectively.

Divergence dates

The Bayesian phylogenetic trees for cox1 and H3 showed tree topology similarity (ILD test, P = 0.8). Three clades corresponded to the three families—Protonemura, Amphinemura and Nemoura—whereas Indonemoura was divided into two clades—the Mainland China clade, clustered with Protonemura, and the Japanese clade (Fig 2).

The evolutionary divergence between the Nemouridae and Capniidae families was settled at 180 Ma, with a 95% HPD interval of 160 to 198 Ma, in the Jurassic geological period (Fig 2). Genus-level diversifications within Nemouridae occurred in the early and middle Cretaceous. Indonemoura from Japan at 119.0 Ma (95% HPD, 125.8 to 100.2 Ma), Indonemoura from Mainland China at 112.0 Ma (95% HPD, 90.2 to 115.0 Ma), Protonemura at 112.7 Ma (95% HPD, 98.0 to 121.3 Ma), Nemoura at 107.0 Ma (95% HPD, 98.8 to 110.1 Ma) and Amphinemura at 80.0 Ma (95% HPD, 75.1 to 92.0 Ma). The speciation process occurred between 25 Ma (early Paleogene) and 90 Ma (late Crustaceous). Out of 35 events of speciation (i.e. nodes), 16 (45%) occurred during late Crustaceous and 19 (54%) occurred during early Paleogene, broadly overlapping with the formation time of the Japanese Archipelago (15 to 30 Ma). We observed intra-species diversification in I. nohirae, A. decemseta, A. zonata, A. longispina, A. megaloba, N. chinonis, N. uenoi and N. cf. cercispinosa (GMYC > 1 species, S1 Table). These species were divided into two clades (S1 Fig), spatially segregated into eastern and western Japan of the Fossa Magna region during the late Neogene period (20 to 22 Ma). Recent diversifications for Nemoura and Amphinemura species within either eastern or western Japanese branches were additionally revealed by TMRCA analysis of cox1 (see Methods). A. decemseta ranging from 3 to 3.5 Ma (95% HPD, 2.8 to 4.1 Ma); A. zonata, ranging from 3 to 4 Ma (95% HPD, 3.5 to 5 Ma); A. longispina, ranging from 3.6 to 4.5 Ma (95% HPD, 3.9 to 5 Ma); A. megaloba, ranging from 3.5 to 4 Ma (95% HPD, 2.8 to 4 Ma); N. uenoi, ranging from 3 to 4 Ma (95% HPD, 3.5 to 4.2 Ma) and N. cf. cercispinosa, ranging from 3.5 to 4.1 Ma (95% HPD, 3 to 5 Ma), for 1.5% Ma and 3.54% Ma analysis respectively.

Phylogeographic pattern between Nemoura from Japan and North America

DNA sequences in the Japanese clade of Indonemoura (single species, I. nohirae) showed a high homology with those in the Alaskan species of Z. columbiana (COI: KM874174; >93% sequence similarity) and Z. cinctipes (H3: EF622600; >98% sequence similarity) based on blastn results.

Based on the Blast results and the previous reported geographical distribution of these species in Asia and North America, we decided to observe the phylogenetic relationships of these Alaskan specimens (Z. columbiana, Z. cinctipes and P. delicatula) with stoneflies taxa from Japan. The ML phylogenetic trees for both cox1 and H3 (Fig 3) showed that the Indonemoura Japanese clade clustered with three North American species (Z. columbiana, Z. cinctipes and P. delicatula) and the Indonemoura Mainland China clade clustered with the East Asian Nemouridae genera (Nemoura, Protonemura and Amphinemura). The pairwise nucleotide substitution rate based on cox1 between the Indonemoura Japanese clade and Zapada spp. or P. delicatula from North America ranged from 0.13 to 0.15, whereas a higher pairwise nucleotide substitution rate based on cox1 of 0.26 was observed between the Indonemoura Japanese and Mainland China clades (Table 2).

Fig 3. Maximum likelihood trees based on both cox1 and H3 markers for comparison between the East Asia Nemouridae family and three North American Nemourinae species: Zapada cinctipes, Z. columbiana and Podmosta delicatula.

Inserted upper map shows sampling site locations in North America (western USA and Alaska) as black dots. The map was prepared using QGIS v 2.18 under the GNU free documentation License with political boundaries from the Global Database of Administrative Areas (

Table 2. Pairwise nucleotide substitution rate based on cox1 between the East Asian Nemouridae and North American (western USA and Alaskan) species.


We studied mitochondrial cox1 and nuclear H3 gene sequences to determine the patterns of diversification and phylogenetic relationships of species belonging to four genera of stoneflies of the Nemouridae family in the Japanese Archipelago. We estimated the divergence among Nemoura, Amphinemura, Indonemoura and Protonemura to have occurred in the early and mid-Cretaceous (around 100 Ma), which is compatible with previous studies based on fossil records [56], [57]. Our results suggested that these four genera might have dispersed and colonised different areas of the Eurasian continent—including the Japanese landmasses—when they were still connected to the Eurasian continent. Among the four genera, the diversification of Indonemoura occurred earlier (120 Ma) than that of the other genera (<100 Ma), suggesting that it is an ancient genus. The geological isolation of colonised areas [58], the long evolutionary time [59] and poor dispersal ability of Indonemoura [23], [60] might have accounted for their ancient diversification.

Based on the phylogenetic relationships of both molecular markers (cox1 and H3), we observed that the three genera Nemoura, Amphinemura and Protonemura were monophyletic and clustered as three independent groups, as previously observed by morphological systematics [16]. However, Indonemoura was paraphyletic. This genus was divided into two clades corresponding to the Mainland China and the Japanese clades. Surprisingly, the Japanese clade of Indonemoura (single species, I. nohirae) clustered together with North American species (Z. columbiana, Z. cinctipes and P. delicatula), with a low pairwise nucleotide substitution rate (<0.15). The distribution range of these two North America genera covers North America and Eastern Asia. Previous studies suggested that their distribution could be related to the land connection (i.e. the islands) between Alaska and Eastern Asia [15]. Dispersal by island connectivity between Alaska, the Aleutian Islands, the Kamchatka peninsula and the Kuril Islands has been observed in other stonefly families (for instance, Arcynopteryx dichroa (McLachlan, 1872), Capnia nearctica Banks, 1919, Mesocapnia variabilis (Klapálek, 1920) and Nemoura arctica Esben-Petersen, 1910) [61]. However, the distribution of Indonemoura on these islands is unknown.

The complex history of the geological formation of the Japanese Archipelago may provide a possible alternative explanation. The ancestral Japanese landmasses were located on the borders of four major tectonic plates, of which two are continental plates—the Eurasian plate and the North American plate [4] (S2 Fig). The eastern Japanese landmass was located on the North American plate, whereas the western Japanese landmass was located on the Eurasian plate [5]. The dispersal and colonisation of Indonemoura might have occurred from the North American plate to the Eurasian continent or vice versa (from the Eurasian continent to the North American plate) before their geographic separation in an ancient time (around 70 to 80 Ma) [62]. Dispersal events between Eurasian and Japanese landmasses are commonly reported for aquatic insects [10], [63]. Particularly, a dispersal event between North America and the Japanese Archipelago was detected by the phylogenetic relationship of the monophyletic group of caddisflies, Palaeagapetus spp. [9]. However, no prior studies have observed speciation events of aquatic insects associated with geological events that occurred in ancient times (>12 Ma). Our result suggests an ancient divergence time and a distribution pattern of Indonemoura, consistent with a hypothesis of an ancient colonisation influenced by the connection of the Japanese landmass with the North American plate in the Eurasian continent.

Nemouridae species diversification, as has been observed in other species of aquatic insects, such as beetles [10], caddisflies [9], water bugs [14] and mayflies [8], [13], was also observed to be affected by the geological formation of the Japanese Archipelago. The diversification of the Nemouridae species occurred during the Paleogene period (<50 Ma). This geological period is consistent with the movement of landmasses (S2 Fig) about 70 Ma ago [4] and the active geological formation of the Japanese Archipelago around 20 Ma ago [5], which could be the cause of the Nemouridae diversification, as previously reported for the mayfly Dipteromimus flavipterus Tojo and Matsukawa, 2003 (35 Ma) [2].

Indonemoura nohirae is the single species of Indonemoura on the Japanese Archipelago [25], [26]. The morphology of their terminalia resembles that of Protonemura rather than of Indonemoura, but the characteristic gill formula justifies their taxonomical classification in Indonemoura [25], [26]. To date, there are 24 Indonemoura species from China [16], [24] and 30 species belonging to the Himalayan and Oriental regions in East Asia [15], [20]. These species are morphologically different from I. nohirae in Japan [15], [16], [20], [24], [25], [26]. We hypothesise that the Indonemoura species of East Asia could be forming separate phylogenetic clades clustered by geographical regions. For the hypothesis testing, further collection of molecular data on Indonemoura from wider areas such as Northeast China, Southeast China, Mongolia, Russia and other countries in Asia is needed in future studies.

Eight species (I. nohirae, A. decemseta, A. zonata, A. longispina, A. megaloba, N. chinonis, N. uenoi and N. cercispinosa) showed interesting patterns of intra-species separation into two genetic groups corresponding to eastern and western areas of the Fossa Magna region of Honshu Island (S1 Fig). Honshu is the centre of insect biodiversity [10]; apart from its extensive territorial space, it is the main island with a geological history [3], [4], [5]. We found supporting evidence on the genetic diversity of these eight species. We found a larger mean nucleotide substitution rate and haplotype number in the Honshu region than in other islands (Table 1). The mean nucleotide substitution rate and haplotype diversity are indications of biodiversity [64], which could lead to evidence of speciation [65]. Out of eight species, the diversification of six species (A. decemseta, A. zonata, A. longispina, A. megaloba, N. uenoi and N. cercispinosa) occurred during the late Neogene period (20 to 22 Ma). This event corresponded with the double-door (i.e. the union of eastern and western Japan; S2 Fig) geological model and the formation of the Itoigawa-Shizuoka tectonic line (ISLT) at around 20 Ma [5], [66]. The speciation of aquatic insects was often observed to be influenced by these two geological events [2]. Additionally, species diversification—from eastern or western Japan of the Fossa Magna region—showed recent diversification events (3 to 5 Ma) corresponding with the formation of the small islands in northeastern or southwestern edge areas of Japan (Fig 1). The northeastern islands created land bridges between the Japanese Archipelago and China or Korea, whereas the southwestern islands connected Taiwan or the Philippines with the Japanese Archipelago [5], [66]. This connectivity promoted immigration events in Japan that might have contributed to the formation of the current genetic diversity, as previously observed in mayflies [13] and beetles [10].

The evolutionary divergence of the Nemouridae family was promoted by the complex geological formation of the Japanese Archipelago. Despite the different evolutionary rate of both molecular markers, Bayesian analysis found congruence between them; however, failed to find congruence with their morphological taxonomy. The main morphological character used for identification of adult stoneflies species is its genital morphology. The evolution of genital morphology is; however, governed by within-population sexual selection rather than environmental or geological history of the locations [67]. Conversely, the genetic variation of natural populations has been observed to be directly associated with environmental [68] and geological variations [2]. Therefore, the genetic variation could reflect an independent course in the evolutionary history of Indonemoura than do the morphological characters used for their taxonomy. However, we detected that N. sanbena shared haplotypes from different lineages, revealing a possible introgression or incomplete sorting of ancestral polymorphisms [10]. This is an often reported phenomenon in stoneflies [40], [69], [70], which remains as unresolved species. Resolving the problems between the process of evolution of morphological characters and the genetic variation within species will improve our future understanding of the origin of the species and the local species distribution.

Finally, our inference of divergence time was based on the coalescent simulation approach. Despite the frequent use of this approach, a biased sampling of lineages and extreme state-dependent molecular substitutions rate heterogeneity are known to potentially cause erroneous inference of divergence time [71]. One of the causes of biased sampling is under-sampling (i.e. the incomplete-coverage samples included in the phylogenetic tree). Previous studies demonstrated that under-sampling increases the estimates of the posterior probabilities (i.e. variance of age estimates become less precise) [72] and led to bias and low precision of the divergence time of shallow nodes (i.e. evolutionary recently divergent taxa) [73], [74]. However, under-sampling tends not to affect deep nodes (i.e. internal nodes close to the root) time scales estimations or the tree shape [75], [76], [77]. Therefore, in order to confirm the accuracy of the time scales estimations of the recently divergent taxa in our study, additional taxonomic samples would be required to be included in the molecular clock analysis. Conversely, the state-dependent molecular substitution rate heterogeneity could be address by combining node calibrations generated by more than one calibration analyses, as recommended by [71], [78]. A cautious method such as the combined uses of fossil records and biogeographic ages as employed in our analysis may minimize the risk of such erroneous inference.

Supporting information

S1 Table. Location information of the samples of East Asia Nemouridae.

Numbers of individuals (N), presence of male (M), female (F) and imago (im), DNA-species delimitation (GMYC).


S1 Fig. Concatenated Bayesian phylogeny (cox1 + H3) for East Asian Nemouridae family enlarging intra-species diversification in I. nohirae, A. decemseta, A. zonata, A. longispina, A. megaloba, N. chinonis, N. uenoi and N. cf. cercispinosa (GMYC = 2 species).


S2 Fig. Putative formation of the Japanese Archipelago [2], [3], [4], [5].

(A) Around 30 to 130 Ma, the Japanese landmasses were located in two major tectonic plates from the Eurasian continent. (B) Around 15 to 30 Ma, the Japanese landmasses began to separate from Eurasia and the North American Plates began to separate from the Eurasian continent, and remained separated by a sea zone called Fossa Magna—a geological event called double-door. (C) Current map of the Japanese Archipelago in East Asia, where the names of the four main Japanese islands and the two tectonic lines are shown. The maps was prepared using QGIS v 2.18 under the GNU free Documentation License with political boundaries from the Global Database of Administrative Areas (



We thank the following colleges for contributing Nemouridae specimens for our analysis: Akatsuki Yoshinari, Kobayashi Kyota, Weihai Li and Boris C. Kondratieff. We also acknowledge anonymous reviewers for constructive comments on an earlier version of the manuscript.


  1. 1. Konstantinov AS, Korotyaev BA Volkovitsh MG. Insect diversity in the Palearctic region. In: Foottit R, Adler P, editors. Insect Biodiversity: Science and Society; 2009, pp. 107–162. Blackwell Publishing.
  2. 2. Tojo K, Sekine K, Takenaka M, Isaka Y, Komaki S, Suzuki T, et al. Species diversity of insects in Japan: their origins and diversification processes. Entomol Sci. 2017;20: 357–381.
  3. 3. Otofuji Y, Matsuda T, Nohda S. Opening mode of the Japan Sea inferred from paleomagnetism of the Japan arc. Nature. 1985;317: 603–604.
  4. 4. Taira A. Tectonic evolution of the Japanese Island Arc system. Annu Rev Earth Planet Sci. 2001;29: 109–134.
  5. 5. Yanai S, Aoki K, Akahori Y. Opening of Japan Sea and major tectonic lines of Japan: MTL, TTL and Fossa Magna. J Geography, 2010;119: 1079–1124.
  6. 6. Avise JC. Phylogeography: the history and formation of species. 1st ed. Cambridge, MA, Harvard University Press; 2000.
  7. 7. Condamine FL, Clapham ME, Kergoat GJ. Global patterns of insects diversification: towards a reconciliation of fossil and molecular evidence?. Sci Rep. 2016;6: 19208. pmid:26778170
  8. 8. Saito R, Tojo K. Complex geographic and habitat based niche partitioning of an East Asian habitat generalist mayfly Isonychia japonica (Ephemeroptera, Isonychiidae), with reference to differences in genetic structure. Freshwater Sci. 2016;35: 712–723.
  9. 9. Tojo K, Itoh T. The establishment patterns of the insect fauna of Japan, in comparison to its geological history. In: Oba Y, Osawa S, editors. The Wonderful and Marvelous World of Insects from the Perspective of Genetic Analyses, Insect DNA Research Society Japan; 2015, pp 105–150. Yushokan, Tokyo.
  10. 10. Sota T, Nagata N. (2008) Diversification in a fluctuating island setting: rapid radiation of Ohomopterus ground beetles in the Japanese Islands. Philos Trans R Soc Lon B Biol Sci. 2008;363: 3377–3390. pmid:18765360
  11. 11. Tominaga O, Su Z-H, Kim C-G, Okamoto M, Imura Y, Osawa S. Formation of the Japanese carabina fauna inferred from a phylogenetic tree of mitochondrial ND5 gene sequences (Coleoptera, Carabidae). J Mol Evol. 2000:50: 541–549. pmid:10835484
  12. 12. Tokuda M, Tanaka S, Zhu D-H. Multiple origins of Locusta migratoria (Orthoptera: Acrididae) in the Japanese archipelago and the presence of two major clades in the world: evidence from a molecular approach. Biol J Linn Soc. 2010;99: 570–581.
  13. 13. Sekine K, Hayashi F, Tojo K. Phylogeography of the East Asian polymitarcyid mayfly genus Ephoron (Ephemeroptera: Polymitarcyidae): a comparative analysis of molecular and ecological characteristics. Biol J Linn Soc. 2013;109: 181–202.
  14. 14. Suzuki T, Kitano T, Tojo K. Contrasting genetic structure of closely related giant water bugs: phylogeography of Appasus japonicus and Appasus major (Insecta: Heteroptera, Belostomatidae). Mol Phylogenet Evol. 2014;72: 7–16. pmid:24398367
  15. 15. Baumann RW. Revision of the stonefly family Nemouridae (Plecoptera): a study of the World Fauna at the generic level. Smithson Contr Zool. 1975;211: 1–74pp.
  16. 16. DeWalt RE, Maehr MD, Neu-Becker U, Stueber G. Plecoptera Species File Online; 2018 [cited 6 February 2018]. Version 5.0/5.0. Available from:
  17. 17. Grubbs SA, Baumann RW, DeWalt RE, Tweddale T. A review of the Nearctic genus Prostoia (Ricker) (Plecoptera, Nemouridae), with the description of a new species and a surprising range extension for P. hallasi Kondratieff & Kirchner. ZooKeys. 2014;401: 11–30.
  18. 18. Verdone CJ, Kondratieff BC, DeWalt RE, South EJ. Studies on the stoneflies of Georgia with the description of a new species of Soyedina Ricker, new state records and an annotated checklist. Illiesia. 2017;13: 30–49.
  19. 19. Li WH, Murányi D, Yang D. Two new species of Protonemura (Plecoptera: Nemouridae) from China, with biogeographical notes on the genus. Zootaxa. 2017;4258: 60–68. pmid:28609934
  20. 20. Murányi D, Li WH. Two new species of stoneflies (Plecoptera: Nemouridae) from Northeastern India, with a checklist of the family in the Indian Subcontinent. Zootaxa. 2013;3694: 167–177. pmid:26312279
  21. 21. Zhiltzova LA. Plecoptera, Gruppe Euholognatha. Fauna of Russia and Neighbouring Countries, New Series. 2003;145: 1–538.
  22. 22. Zhiltzova LA, Teslenko VA. Zapada Ricker, 1952 –a genus of Nemourinae (Plecoptera: Nemouridae) new for Asia. Russian Entomol J. 2001;10: 125–128.
  23. 23. Kawai T, Tanida K. Aquatic insects of Japan: Manual with keys and illustration. Tokai University Press, Japan; 2005.
  24. 24. Yang D, Li WH, Zhu F. Plecoptera: Nemouroidea. Fauna Sinica. 2015;58: 1–518.
  25. 25. Shimizu T. Indonemoura nohirae (Okamoto, 1922), comb. n. (Plecoptera, Nemouridae) newly recorded from Japan, with a redescription of Amphinemura longispina (Okamoto, 1922). Jap J Entomol. 1994;62: 619–627.
  26. 26. Shimizu T. Taxonomic changes and synonyms for the East Asian species of the genus Nemoura (Plecoptera: Nemouridae). Aquat Insects. 1994;16: 213–225.
  27. 27. Shimizu T. New name of an Amphinemura species for Nemoura (Protonemura) spinosa Kawai, 1960, with description of a new species from Japan (Plecoptera, Nemouridae). Jap J Entomol. 1997;65: 793–798.
  28. 28. Shimizu T. The species of the Nemoura ovocercia group (Plecoptera: Nemouridae). Aquat Insects. 1997;19: 193–218.
  29. 29. Shimizu T. Two new species of the genus Amphinemura from Japan and Taiwan (Plecoptera, Nemouridae). Jap J Entomol. 1997;3: 77–84.
  30. 30. Shimizu T. (1998) The genus Protonemura in Japan (Insecta: Plecoptera: Nemouridae). Spec Div. 1998;3: 133–154.
  31. 31. Shimizu T. The group of Amphinemura flavostigma (Plecoptera, Nemouridae). Aquat Insects. 1998;20: 203–208.
  32. 32. Shimizu T. The group of Amphinemura megaloba (Plecoptera, Nemouridae). Jap J Entomol. 1998;4: 227–236.
  33. 33. Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol. 1994;3: 294–297. pmid:7881515
  34. 34. Colgan DJ, McLauchlan A, Wilson GDF, Livingston SP, Edgecombe GD, Macaranas J, et al. Histone H3 and U2 snRNA DNA sequences and arthropod molecular evolution. Aust J Zool. 1998;46: 419–437.
  35. 35. Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, et al. Clustal W and Clustal X version 2.0. Bioinformatics. 2007;23: 2947–2948. pmid:17846036
  36. 36. Librado P, Rozas J. DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009;25: 1451–1452. pmid:19346325
  37. 37. Fujisawa T, Barraclough TG. Delimiting species using single-locus data and the generalized mixed yule coalescent approach: a revised method and evaluation on simulated data sets. Syst Biol. 2013;62; 707–724. pmid:23681854
  38. 38. Drummond AJ, Suchard MA, Xie D, Rambaut A. Bayesian phylogenetics with BEAUti and the BEAST 1.7. Mol Biol Evol. 2012;29; 1969–1973. pmid:22367748
  39. 39. Ezard T, Fujisawa T, Barraclough T. Splits: SPecies lImits; 2014. Available from:
  40. 40. Bouckaert R, Heled J, Kuhnert D, Vaughan T, Wu C-H, Xie D. et al. BEAST 2: A Software Platform for Bayesian Evolutionary Analysis. PLoS Comput Biol. 2014;10: e1003537. pmid:24722319
  41. 41. Misof B, Shanlin L, Meusemann K, Peters RS, Donath A, Mayer C. et al. Phylogenomics resolves the timing and pattern of insect evolution. Science. 2014;346: 763–767. pmid:25378627
  42. 42. Murányi D, Gamboa M, Orci KM. Zwicknia gen. n., a new genus for the Capnia bifrons species group, with descriptions of three new species based on morphology, drumming signals and molecular genetics, and a synopsis of the West Palearctic and Nearctic genera of Capniidae (Plecoptera). Zootaxa. 2014;3812: 1–82.
  43. 43. Drummond AJ, Ho SYW, Phillips MJ, Rambaut A. Relaxed phylogenetics and dating with confidence. PLoS Biol. 2006;4: 699–710.
  44. 44. Zessin W. Variabilität, Merkmalswandel und Phylogenie der Elcanidae im Jungpaläozoikum und Mesozoikum und die Phylogenie der Ensifera (Orthopteroida, Ensifera). Dtsch Entomol Z. 2008;34: 1–76.
  45. 45. McCulloch GA, Wallis GP, Waters JM. A time-calibrated phylogeny of southern hemisphere stoneflies: testing for Gondwanan origins. Mol Phylogenetics Evol. 2016;96: 150–160.
  46. 46. Heath TA, Huelsenbeck JP, Stadler T. The fossilized birth-death process for coherent calibration of divergence-time estimates. Proc Natl Acad Sci U S A. 2014;111: E2957–E2966. pmid:25009181
  47. 47. Heled J, Drummond AJ. Calibrated tree priors for relaxed phylogenetics and divergence time estimation. Syst Biol. 2012;61: 138–149. pmid:21856631
  48. 48. Farrell BD. Evolutionary assembly of the milkweed fauna: cytochrome oxidase I and the age of Tetraopes beetles. Mol Phylogenetics Evol. 2001;18: 467–478.
  49. 49. Papadopoulou A, Anastasiou I, Vogler AP Revisiting the insect mitochondrial molecular clock: the mid-Aegean trench calibration. Mol Biol Evol. 2010;27: 1659–1672. pmid:20167609
  50. 50. Rambaut A, Drummond A.J. Tracer v1.4; 2007. Available from:
  51. 51. Rambaut, A. FigTree v. 1.3.1; 2009. Available from:
  52. 52. Farris JS, Kallersjo M, Kluge AG, Bult C. Testing significance of incongruence. Cladistics. 1994;10: 315–319.
  53. 53. Nixon KC. The parsimony ratchet, a new method for rapid parsimony analysis. Cladistics. 1999;15: 407–414.
  54. 54. Guindon S, Gascuel O. PhyML: A simple, fast and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol. 2003;52: 696–704. pmid:14530136
  55. 55. Posada D. jModelTest: Phylogenetic Model Averaging. Mol Biol Evol. 2008;25: 1253–1256. pmid:18397919
  56. 56. Liu Y-S, Sinitshenkova ND, Ren D. A revision of the Jurassic stonefly genera Dobbertiniopteryx Ansorge and Karanemoura Sinitshenkova (Insecta: Plecoptera), with the description of new species from the Daohugou locality, China. Paleontol J. 2009;43: 183–190.
  57. 57. Yushuang L, Sinitshenkova ND, Dong R, Chungkun S. Pronemouridae fam. nov. (Insecta: Plecoptera), the stem group of Nemouridae and Notonemouridae, from the middle of Jurassic of inner Mongolia, China. Palaentology. 2011;54: 923–933.
  58. 58. Gustafson GT, Prokin AA, Bukontaite R, Bergsten J, Miller KB. Tip-dated phylogeny of whirligig beetles reveals ancient lineages surviving on Madagascar. Sci Rep. 2017;7: 8619. pmid:28831048
  59. 59. Brown RM, Siler CD, Oliveros CH. Esselstyn JA, Diesmos AC, Hosner PA, et al. Evolutionary process of diversification in a Model Island Archipelago. Ann Rev Ecol Evol Syst. 2013;44: 411–435.
  60. 60. Shimizu, T. Biodiversity of Asian streams with particular reference to stonefly studies in Japan. In: Bae Y, editor. The 21st Century and Aquatic Entomology in East Asia. Proceedings of the 1st Symposium of AESEA; 2001. pp 11–19. Korean Society of Aquatic Entomologists.
  61. 61. Teslenko VA. Stoneflies (Plecoptera) of the Russian Far East: diversity and zoogeography. Aquat Insects. 2009;31: 693–706.
  62. 62. Condie K.C Plate tectonic and crustal evolution. 4th ed. Butterworth Heinemann. Great Britain; 1997.
  63. 63. Su ZH, Ohama T, Okada TS, Nakamura K, Ishikawa R, Osawa S. Geography-linked phylogeny of the Damaster ground beetles inferred from mitochondrial ND5 gene sequences. J Mol Evol. 1996;43: 662–671. pmid:8995063
  64. 64. Goodall-Copestake WP., Tarling GA., Murphy EJ. On the comparison of population-level estimates of haplotype and nucleotide diversity: a case of study using the gene cox1 in animals. Heredity. 2012;109(1): 50–56. pmid:22434013
  65. 65. Hague MT, Routman EJ. Does population size affect genetic diversity? A test with sympatric lizard species. Heredity. 2016;116: 92–98. pmid:26306730
  66. 66. Ninomiya T, Shimoyama S, Watanabe K, Horie K, Dunkley DJ, Shiraishi K. Age of the Taishu Group, southwestern Japan, and implications for the origin and evolution of the Japan Sea. Island Arc. 2014;3: 206–220.
  67. 67. Hosken DJ, Stockley P. Sexual selection and genital evolution. Trends Ecol Evol. 2004;19: 87–93. pmid:16701234
  68. 68. Schoville SD, Bonin A, Francois O, Lobreaux S, Melodelima C, Manel S. Adaptive genetic variation on the landscape: Methods and cases. Ann Rev Ecol Evol Syst. 2012;43: 23–43.
  69. 69. Boumans L, Hogner S, Brittain J, Johnsen A. Ecological speciation by temporal isolation in a population of the stonefly Leuctra hippopus (Plecoptera, Leuctridae). Ecol Evol. 2017;7: 1635–1649. pmid:28261472
  70. 70. Viteck S, Vincon G, Graf W, Pauls SU. High cryptic diversity in aquatic insects: an integrative approach to study the enigmatic Leuctra inermis species group (Plecoptera). Arthropod Syst Phylo. 2017;75: 497–521.
  71. 71. Beaulieu JM, O'Meara BC, Crane P, Donoghue MJ. Heterogeneous rates of molecular evolution and diversification could explain the Triassic age estimate for angiosperms. Syst Biol. 2015;64: 869–878. pmid:25944476
  72. 72. Linder HP, Hardy CR, Rutschmann F. Taxon sampling effects in molecular clock dating: An example from the African Restionaceae. Mol Phylogenet Evol. 2005;35: 569–582. pmid:15878126
  73. 73. Tuinen M, Torres CR. Potential for bias and low precision in molecular divergence time estimation of the Canopy of Life: an example from aquatic bird families. Front. Genet. 2015;6: 203 pmid:26106406
  74. 74. Marin J, Hedges SB. Undersampling genomes has biased time and rate estimates throughout the tree of life. Molecular biology and evolution. 2018;35: 2077–2084. pmid:29846659
  75. 75. Hug LA, Roger AJ. The impact of fossils and taxon sampling on ancient molecular dating analyses. Mol Biol Evol. 2007;24: 1889–97. pmid:17556757
  76. 76. Xiang QY, Thomas DT, Xiang QP. Resolving and dating the phylogeny of Cornales—Effects of taxon sampling, data partitions, and fossil calibrations. Mol Phylogenet Evol. 2011;59: 123–38. pmid:21300164
  77. 77. Soares AER, Schrago CG. The influence of taxon sampling and tree shape on molecular dating: and empirical example from mammalian mitochondrial genomes. Bioinform Biol Insights. 2012;6: 129–143. pmid:22693422
  78. 78. Barba-Montoya J, dos Reis M, Yang Z. Comparison of different strategies for using fossil calibrations to generate the time prior in bayesian molecular clock dating. Mol Phylogenet Evol. 2017;114: 386–400. pmid:28709986