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Simple Summary: Hylidae is a rich family of Anura that is widely distributed across the world. Previous studies have shown that the Hyla and Dryophytos genera in the Hylidae used to belong to the same genus. The Eurasian species (including Hyla sanchiangensis) originated in North America and spread through the Beringian Land Bridge to Asia during the last ice age. Adaptation to low temperatures may require more energy expenditure. Mitochondria are the center of energy metabolism and, through oxidative phosphorylation, provide most of the ATP energy for the physiological and biochemical activities of the body. The mitogenome was used to investigate whether Hyla and Dryophytos genera are subject to positive selection. In addition, as a unique species in China, the distinction between Hyla sanchiangensis (Anura: Hylidae) and two different sites was also compared and analyzed in this paper. Hyla sanchiangensis (Anura: Hylidae) is endemic to China and is distributed across Anhui, Zhejiang, Fujian, Guangdong, Guangxi, Hunan, and Guizhou provinces. The mitogenomes of H. sanchiangensis from two different sites (Jinxiu, Guangxi, and Wencheng, Zhejiang) were sequenced. Phylogenetic analyses were conducted, including 38 mitogenomes of Hylidae from the NCBI database, and assessed the phylogenetic relationship of H. sanchiangensis within the analyzed dataset. Two mitogenomes of H. sanchiangensis showed the typical mitochondrial gene arrangement with 13 protein-coding genes (PCGs), two ribosomal RNA genes (12S rRNA and 16S rRNA), 22 transfer RNA (tRNA) genes, and one non-coding control region (D-loop). The lengths of the 12S rRNA and 16S rRNA genes from both samples (Jinxiu and Wencheng) were 933 bp and 1604 bp, respectively. The genetic distance (p-distance transformed into percent) on the basis of the mitogenomes (excluding the control region) of the two samples was calculated as 4.4%. Hyla sanchiangensis showed a close phylogenetic relationship with the clade of (H. annectans + H. tsinlingensis), which was supported by ML and BI analyses. In the branch-site model, five positive selection sites were found in the clade of Hyla and Dryophytes: Cytb protein (at position 316), ND3 protein (at position 85), and ND5 protein (at position 400) have one site, respectively, and two sites in ND4 protein (at positions 47 and 200). Based on the results, we hypothesized that the positive selection of Hyla and Dryophytes was due to their experience of cold stress in historical events, but more evidence is needed to support this conclusion. [ABSTRACT FROM AUTHOR]

The complete mitochondrial (mt) genome of Leptomantella tonkinae (Hebard, 1920) was 15,527 bp in length and contained 13 protein-coding genes, 22 transfer RNAs, two ribosomal RNAs, and one control region. The gene arrangement of mt genome of L. tonkinae was identical to the primitive mantis. The overall AT content of the mt genome was 74%. In ML and BI phylogenetic analyses, the monophyly of Leptomantellidae was robustly supported and the clade of Leptomantellidae is a sister clade to the group of (Gonypetidae+(Leptomantellidae+(Amorphoscelidae+Nanomantidae))). [ABSTRACT FROM AUTHOR]

The phylogenetic relationship of Ephemeridae (Insect: Ephemeroptera) remains hotly debated using mitochondrial (mt) genomes. All previously reported mt genomes of Ephemeridae belong to the genus Ephemera. This study provides the first complete mt genome sequence from the genus Hexagenia with an analysis of the mitogenome of Hexagenia rigida Mc Dunnough, 1924 (Ephemeroptera: Ephemeridae) and providing new information to discuss the phylogenetic relationships within Ephemeroptera. The complete mt genome of H. rigida was a circular molecule of 16,159 bp in length, containing 37 genes (2 rRNA genes, 13 protein-coding genes, 22 tRNA genes), which showed the typical mt gene arrangement of insects. The AT content of the whole genome was 70.0% and the length of the control region was 1091 bp. All protein-coding genes used ATN as the start codon, and most PCGs used TAA/TAG as the stop codons excluding COI, COII, ND5 and Cyt b that used T as the stop codon. BI and ML phylogenetic trees constructed from 27 species of 13 families showed that Ephemeridae is a sister clade to the clade Polymitarcyidae. [ABSTRACT FROM AUTHOR]

Rana johnsi (Smith 2009) firstly considered as the member of genus Pseudorana, has been moved into the genus Rana. In this study, we sequenced the complete mitochondrial (mt) genome of R. johnsi using the Sanger method. The circular mt genome was 17,873 bp in length and contains 13 protein-coding genes (PCGs), 22 transfer RNA (tRNA) genes, two ribosome RNA genes, and one control region. The overall nucleotide composition in majority-strand was 28% A, 29% T, 29% C, and 14% G. We discussed the phylogenetic relationship of R. johnsi in genus Rana using ML and BI analyses based on 13 PCGs. Excluding the clade of subgenus Lithobates, Rana draytonii was the basal clade to all other Rana species, which included R. johnsi as the basal clade. The monophyly of genus Rana was supported, whereas Pseudorana was failed to support. [ABSTRACT FROM AUTHOR]

The first complete mitochondrial genome of Euroleon coreanus (Okamoto, 1926) was 15,797 bp in length, and contained 13 protein-coding genes, 22 transfer RNAs, two ribosomal RNAs, and the control region. Compared to the classic insect mitochondrial genome, E. coreanus showed a gene rearrangement of ND2-C-W-Y-COX1. The overall AT content of the mitochondrial genome was 75.5%. The monophyly of Ascalaphidae, Myrmeleontidae, Nemopteridae, Nymphidae, and Psychopsidae was supported in both BI and ML trees. And E. coreanus was a sister clade to the clade of genus Myrmeleon. [ABSTRACT FROM AUTHOR]

Zoodes fulguratus is a common species of Cerambycidae, reported from Vietnam, Nepal, Laos, Burma, and China. To date, no mitochondrial genomes of the genus Zoodes have been reported. In this study, we sequenced and analyzed the first mitochondrial genome of Z. fulguratus to discuss its phylogenetic relationship within the subfamily Cerambycinae. This mitochondrial genome showed the typical insect gene arrangement: a circular molecule of 15,885 bp long with 13 protein-coding genes, two ribosomal RNA genes (rRNAs), and 22 transfer RNA genes (tRNAs). The AT content of the whole mitogenome was 74.2% with a high asymmetric nucleotide presentation revealed by a positive AT-skew (0.067) and a negative GC-skew (–0.178), whereas the AT content of the A + T rich region was 80%. The Maximum likelihood (ML) and Bayesian inference (BI) phylogenetic analyses showed that Z. fulguratus is a sister clade of Gnatholea eburifera. [ABSTRACT FROM AUTHOR]

The mitochondrial genome of Teratoscincus roborowskii (Squamata: Gekkonidae) (GenBank No. MT107158) was a circular molecule of 16,693 bp in length, including 13 protein-coding genes, 2 ribosomal RNA genes, 22 transfer RNA genes, and 1 non-coding region (control region). The overall base composition of the H-strand of T. roborowskii is 30.6% A, 25.6% T, 29.7% C, 14.1% G, respectively. Phylogenetic analyses showed that T. roborowskii (MT107158) was a sister clade to T. keyserlingii whereas Teratoscincus roborowskii (KP115216) was a close sister clade of T. keyserlingii and T. roborowskii (MT107158). [ABSTRACT FROM AUTHOR]

The complete mitochondrial genome of the Annamanum lunulatum is 15,610 bp in length, which contains 13 protein-coding genes, 22 transfer RNAs, two ribosomal RNAs, and the A + T-rich region. The arrangement of genes is identical to all know longhorn beetles mitochondrial genomes. The overall AT content of the mitochondrial genome is 75.3%, whereas the AT content of A + T-rich region is 84.3%. In ML and BI phylogenetic analyses, A. lunulatum is a sister clade to Blepephaeus succinctor, and the monophyly of Lamiinae is supported. [ABSTRACT FROM AUTHOR]

The complete mitochondrial genome of Mantis religiosa (Mantodea: Mantidae) from Canada was successfully sequenced. The mitochondrial genome was a circular molecule of 15,521 bp in length, containing 13 protein-coding genes, two rRNA genes, 23 tRNA genes (including an extra tRNAArg gene), and the control region. The AT content of the whole genome was 76.9% and the length of the control region was 636 bp with 81.9% AT content. The structure of the M. religiosa mitochondrial genome from Canada was almost identical to M. religiosa from China and their genetic distance was just 0.017. In Bayesian inference (BI) and maximum likelihood (ML) analyses, we found that M. religiosa was a sister clade to Statilia sp. and the monophyly of the genera Hierodula and Rhombodera was not supported. [ABSTRACT FROM AUTHOR]

The relationship of Matrona and Atrocalopteryx (Odonata: Calopterygidae) is still unclear. To better understand the phylogenetic relationship of Matrona and Atrocalopteryx, we sequenced and annotated two complete mitochondrial genomes of Matrona basilaris sampled from two different locations. The length of the two complete mitochondrial genomes of M. basilaris is 16,149 bp and 15,893 bp for the specimens collected in Jinhua, Zhejiang Province and Tianmushan, Zhejiang Province, China, respectively. The two mitochondrial genomes include the typical invertebrate set of 37 genes: 13 protein-coding genes (PGCs), 22 tRNA genes, and 2 rRNA genes. The nucleotide composition of the mitogenome is similar to other odonates with high content of A + T (68.9%) and all PCGs use ATN as the start codon. Tandem repeats were detected in the control regions of the two M. basilaris samples that accounted for the different sequence lengths of the mitochondrial genomes from the two locations. Finally, BI and ML phylogenetic analysis based on the concatenated nucleotide sequences of the 13 PCGs supported the conclusion that M. basilaris is a sister clade to Atrocalopteryx melli. [ABSTRACT FROM AUTHOR]

The complete mitochondrial genome of Xystrocera globosa is 15,706 bp in length, containing 13 protein-coding genes, 22 transfer RNAs, two ribosomal RNAs and the A + T-rich region. The overall base composition is 72.7% AT and 27.3% GC, and the AT content of the control region is 79.3%. In ML and BI phylogenetic trees, X. globosa was a sister clade to X. grayii. The monophyly of Lamiinae and Prioninae were supported in ML analyses, but nevertheless, the monophyly of Cerambycinae was not recovered. [ABSTRACT FROM AUTHOR]

The mitochondrial genome of Fejervarya kawamurai is a circular molecule of 17,650 bp in length, containing 13 protein-coding genes, two rRNA genes, 23 tRNA genes (including an extra tRNA-Met), and the control region. The AT content of the whole genome is 56.9%. In Bayesian inference (BI) and Maximum likelihood (ML) analyses, we found that F. kawamurai is a sister clade to F. multistriata and F. limnocharis. The monophyly of Fejervarya, Quasipaa, Nanorana was well supported (1.00 in BI and 100% in ML). [ABSTRACT FROM AUTHOR]

The complete mitochondrial genome of Choroterpides apiculata (Ephemeroptera: Leptophlebiidae) is typically a circular molecule of 15,199 bp in length, containing 37 genes (13 protein-coding genes, 22 tRNAs, and two rRNAs) and one control region. The overall A + T content of the whole genome is 74% and the A + T content of the control region is 79.7%. In Bayesian inference and maximum-likelihood phylogenetic trees using 24 species from 13 families of Ephemeroptera, the monophyly of the families Isonychiidae, Heptageniidae, Vietnamellidae, Leptophlebiidae, Caenidae, and Baetidae were highly supported and C. apiculata was a sister group to Habrophlebiodes zijinensis. [ABSTRACT FROM AUTHOR]

Abstract: The mt genome of Paa spinosa (Anura: Ranoidae) is a circular molecule of 18,012 bp in length, containing 38 genes (including an extra copy of tRNA-Met gene). This mt genome is characterized by three distinctive features: a cluster of rearranged tRNA genes (LTPF tRNA gene cluster), a tandem duplication of tRNA-Met gene (Met1 and Met2), and distinct repeat regions at both 5′ and 3′-sides in the control region. Comparing the locations and the sequences of all tRNA-Met genes among Ranoidae, and constructing NJ tree of the nucleotide of those tRNA-Met genes, we suggested a tandem duplication of tRNA-Met gene can be regarded as a synapomorphy of Dicroglossinae. To further investigate the phylogenetic relationships of anurans, phylogenetic analyses (BI, ML and MP) based on the nucleotide dataset and the corresponding amino acid dataset of 11 protein-coding genes (except ND5 and ATP8) arrived at the similar topology. [Copyright &y& Elsevier]

Simple Summary: The family Scarabaeidae is one of the largest families in the insect order Coleoptera and is comprised of two quasi-systematics groups, Pleurosticti and Laparosticti. Pleurosticti is an economically important scarab group comprising about 20,000 species, the majority of which are phytophagous. Despite the innumerable studies based on ecological, molecular, and morphological characteristics, their taxonomy is still unclear and subject to many scientific hypotheses. The mitochondrial (mt) genome can provide tangible information to resolve the phylogenetic relationships within the family Scarabaeidae. However, the available mt genomes of Scarabaeidae in GenBank are underrepresented. Thus, we sequenced and analyzed 18 new phytophagous Scarabaeidae mitochondrial genomes from two subfamilies, Cetoniinae and Dynastinae, to conduct phylogenetic analyses within Scarabaeidae. This study contributes to increasing our knowledge about phytophagous Scarabaeidae. The availability of next-generation sequencing (NGS) in recent years has facilitated a revolution in the availability of mitochondrial (mt) genome sequences. The mt genome is a powerful tool for comparative studies and resolving the phylogenetic relationships among insect lineages. The mt genomes of phytophagous scarabs of the subfamilies Cetoniinae and Dynastinae were under-represented in GenBank. Previous research found that the subfamily Rutelinae was recovered as a paraphyletic group because the few representatives of the subfamily Dynastinae clustered into Rutelinae, but the subfamily position of Dynastinae was still unclear. In the present study, we sequenced 18 mt genomes from Dynastinae and Cetoniinae using next-generation sequencing (NGS) to re-assess the phylogenetic relationships within Scarabaeidae. All sequenced mt genomes contained 37 sets of genes (13 protein-coding genes, 22 tRNAs, and two ribosomal RNAs), with one long control region, but the gene order was not the same between Cetoniinae and Dynastinae species. All mt genomes of Dynastinae species showed the same gene rearrangement of trnQ-NCR-trnI-trnM, whereas all mt genomes of Cetoniinae species showed the ancestral insect gene order of trnI-trnQ-trnM. Phylogenetic analyses (IQ-tree and MrBayes) were conducted using 13 protein-coding genes based on nucleotide and amino acid datasets. In the ML and BI trees, we recovered the monophyly of Rutelinae, Cetoniinae, Dynastinae, and Sericinae, and the non-monophyly of Melolonthinae. Cetoniinae was shown to be a sister clade to (Dynastinae + Rutelinae). [ABSTRACT FROM AUTHOR]

The phylogenetic relationship of Caenidae remains hotly debated within the Ephemeroptera. We sequenced the complete mitochondrial genome of Caenis sp. (Ephemeroptera: Caenidae) to discuss the phylogenetic relationships among the Caenidae. The mitochondrial genome of Caenis sp. collected from Jian'ou, Fujian province, China is a circular molecule of 15,392 bp in length containing 37 genes (13 protein-coding genes, 22 tRNAs, and two rRNAs), which showed the typical insect mitochondrial gene arrangement. In BI and ML phylogenetic trees using 23 species from 13 families, the monophyly of the families Caenidae, Heptageniidae, Isonychiidae, and Vietnamellidae was strongly supported. The clade of Caenidae is a sister clade to the clade of Teloganodidae and Baetidae. [ABSTRACT FROM AUTHOR]

Simple Summary: The Ephemeroptera is an ancient lineage of insects, among which the Heptageniidae is one of the most species-rich families, although its phylogenetic relationships have been controversial. The mitogenomes of Heptageniidae were found gene rearrangements of CR-I-M-Q-M-ND2 and a conserved intergenic gap between trnA and trnR. Thus, 15 complete and two nearly complete mitogenomes of Heptageniidae were used to explore mitogenome structures and clarify the disputes of phylogenetic relationships among Heptageniidae. Additionally, the Heptageniidae samples collected from habitats with significant temperature differences were applied to investigate the adaptive evolution of mitochondrial PCGs under low-temperature stress. We determined 15 complete and two nearly complete mitogenomes of Heptageniidae belonging to three subfamilies (Heptageniinae, Rhithrogeninae, and Ecdyonurinae) and six genera (Afronurus, Epeorus, Leucrocuta, Maccaffertium, Stenacron, and Stenonema). Species of Rhithrogeninae and Ecdyonurinae had the same gene rearrangement of CR-I-M-Q-M-ND2, whereas a novel gene rearrangement of CR-I-M-Q-NCR-ND2 was found in Heptageniinae. Non-coding regions (NCRs) of 25–47 bp located between trnA and trnR were observed in all mayflies of Heptageniidae, which may be a synapomorphy for Heptageniidae. Both the BI and ML phylogenetic analyses supported the monophyly of Heptageniidae and its subfamilies (Heptageniinae, Rhithrogeninae, and Ecdyonurinae). The phylogenetic results combined with gene rearrangements and NCR locations confirmed the relationship of the subfamilies as (Heptageniinae + (Rhithrogeninae + Ecdyonurinae)). To assess the effects of low-temperature stress on Heptageniidae species from Ottawa, Canada, we found 27 positive selection sites in eight protein-coding genes (PCGs) using the branch-site model. The selection pressure analyses suggested that mitochondrial PCGs underwent positive selection to meet the energy requirements under low-temperature stress. [ABSTRACT FROM AUTHOR]

The complete mitochondrial genome of Isonychia kiangsinensis is a circular molecule of 15,456 bp in length, containing 2 rRNA genes, 13 protein-coding genes, 22 tRNA genes, and a control region. The AT content of the overall base composition is 62.9%. The length of the control region for I. kiangsinensis is 745 bp with 68.6% AT content. In BI and ML phylogenetic trees, Isonychia kiangsinensis was a sister clade to I. ignota and Isonychiidae was shown to be the basal clade of Ephemeroptera excluding Siphluriscidae. The monophyly of the families Isonychiidae, Heptageniidae, Viemamellidae, and Baetidae and the genus Isonychia were well supported. [ABSTRACT FROM AUTHOR]

The mitochondrial genome of Epeorus herklotsi (Ephemeroptera: Heptageniidae) is a circular molecule of 15,801 bp in length with a base composition of 32.7% A, 32.9% T, 21.5% C, 13.0% G, including extra tRNAMet gene. The IMQM tRNA cluster is found in E. herklotsi as well as Parafornuru youi and two species of Epeorus (KM244708, KJ493406), while the typical IQM tRNA cluster is found in Paegniodes cupulatus. In BI and ML phylogenetic trees, the monophyly of the families Heptageniidae, Baetidae, and Ephemerellidae are highly supported. E. herklotsi is a sister clade to Epeorus sp2. (KJ493406). [ABSTRACT FROM AUTHOR]

The complete mitochondrial genome of Psychomantis borneensis (Mantodea: Hymenopodidae) was successfully sequenced. The mitochondrial genome is found to be 15,493 bp long and is a circular molecule containing 37 genes (13 protein-coding genes, 22 tRNAs, and 2 rRNAs), typically found in other mantis mitochondrial genomes. The AT content of the whole genome was 72.4% and the length of the control region was 697 bp with 79.9% AT content. A phylogenetic tree was constructed based on the BI and ML analysis of 16 species of Mantodea. The results showed that P. borneensis was a sister clade to (Anaxarcha zhengi + Creobroter gemmata) (Hymenopodidae). The monophyly of the family Mantidae and the genus Theopompa, Hierodula, and Rhombodera were not supported. The outcome of this study will provide a useful data for population genetics studies as well as serve as a tool for better characterizing phylogenetic analysis of Mantodea. [ABSTRACT FROM AUTHOR]

The complete mitochondrial genome of the thirteen-lined ground squirrel,Ictidomys tridecemlineatus(Rodentia: Sciuridae) was sequenced to analyze the gene arrangement. It is a circular molecule of 16,458 bp in length including 37 genes typically found in other squirrels. The AT content of the overall base composition is 63.7% and the length of the control region is 1016 bp with 63.0% AT content. In BI and ML phylogenetic trees,I. tridecemlineatusis a sister clade to the genusCynomys, andTamias sibiricusis a sister clade to (Marmota himalayana + (I. tridecemlineatus + (C. leucurus + C. ludovicianus))). Ratufinae is well supported as the basal clade of Sciuridae. The monophyly of the family Sciuridae and its subfamilies Callosciurinae, Xerinae and Sciurinae are well supported. [ABSTRACT FROM AUTHOR]

Gene rearrangements have been found in several mitochondrial genomes of Mantodea, located in the gene blocks CR- I-Q-M-ND2 , COX1 - K - D - ATP8 and ND3-A-R-N-S-E-F-ND5. We have sequenced one mitogenome of Amelidae (Yersinia mexicana) and six mitogenomes of Mantidae to discuss the mitochondrial gene rearrangement and the phylogenetic relationship within Mantidae. These mitogenomes showed rearrangements of tRNA genes except for Asiadodis yunnanensis and Hierodula zhangi. These novel gene rearrangements of Mantidae were primarily concentrated in the region of CR- I-Q-M-ND2 , including gene translocation, duplication and pseudogenization. For the occurrences of these rearrangements, the tandem duplication-random loss (TDRL) model and slipped-strand mispairing model were suitable to explain. Large non-coding regions (LNCRs) located in the region of CR- I-Q-M-ND2 were detected in most Mantidae species, whereas some LNCRs had high similarity to the control region (CR). Both BI and ML phylogenetic analyses supported the monophyly of Mantidae and the paraphyly of Mantinae. The phylogenetic results with the gene order and the location of NCRs acted as forceful evidence that specific gene rearrangements and special LNCRs may be synapomorphies for several groups of mantises. [ABSTRACT FROM AUTHOR]

We acquired 21 complete mitogenomes and 6 nearly complete mitogenomes of mantises belonging to 8 families (Hymenopodidae, Iridopterygidae, Mantidae, Metallyticidae, Sibyllidae, Tarachodidae, Thespidae, Toxoderidae) using 14 pairs of mantid specific primer sets and found that 5 species of mantises have duplicate copies (2–4) of trnR : Ambivia undata , Creobroter jiangxiensis , Creobroter urbanus , Phyllothelys sp1. and Theopropus elegans while two novel gene arrangements CR- I -NCR- I -NCR- I -NCR- I -NCR- I -NCR*- Q - M and COII - K* - D* - K - D* - K - D* - K - D were found in Schizocephala bicornis and Stenotoxodera porioni , respectively. The multiple copies of trnR are caused by independent duplications. The gene arrangements in Stenotoxodera porioni with three identical copies of trnK can be explained as mid-way through the TDRL process while the form of gene arrangement in Schizocephala bicornis is unclear. In the phylogeny at the family level, the monophyly of Liturgusidae and Iridopterygidae was supported, whereas the monophyly of Hymenopodidae, Mantidae and Tarachodidae wasn't. The features of mantis mitochondrial genomes including high duplication rates of trnR, trnK and trnI indicate that Mantodea mitochondrial genomes maybe a useful model system for studying gene duplication. However, derived gene arrangements may not be appropriate for phylogenetic inference in Mantodea as they aren't synapomorphy and aren't shared by close relatives. [ABSTRACT FROM AUTHOR]