dcsimg

Trophic Strategy

provided by Fishbase
Carnivorous, feeds mainly on benthic crustaceans and fish (Ref. 30433).
license
cc-by-nc
copyright
FishBase
Recorder
Pascualita Sa-a
original
visit source
partner site
Fishbase

Biology

provided by Fishbase
Carnivorous, feeds mainly on benthic crustaceans and fish (Ref. 30433).
license
cc-by-nc
copyright
FishBase
Recorder
Pascualita Sa-a
original
visit source
partner site
Fishbase

Comprehensive Description

provided by Smithsonian Contributions to Zoology
Cynoglossus semilaevis Günther

Cynoglossus semilaevis Günther, 1873:379 [type-locality: Chefoo, China]; 1898:261 [Nin-Tchouang].—Mori, 1927:183.—Chu, 1931:95.—Wu, 1932:152 [Tsing-Wang-Tao, Tsing-Tao, Tchefoo, Tcha-Pou, Wen Chou, and Amoy].

Areliscus semilaevis.—Jordan and Starks, 1906a:242.

Trulla semilaevis.—Fowler, 1934b:212.

Arelia rhomaleus Jordan and Starks, 1906b:526, fig. 5 [Port Arthur, Manchuria],

Areliscus rhomaleus.—Jordan and Metz, 1913:63.—Reeves, 1927:14 [Swatow].—Sowerby, 1930:183.—Chu, 1931:95.

Cynoglossus roulei Wu, 1932:153 [type-locality: Amoy, China].

DESCRIPTION.—Based on 8 specimens, 134.0–530.0 mm SL, including the holotype of C. semilacvis and syntypes of C. roulei.

Depth of body 24.63–30.19 (M = 27.09), length of head 20.89–26.79 (M = 23.93) percent of standard length. Upper eye not in advance of fixed eye, diameter of eye 3.52–8.11 (M = 5.77), interorbital space rather broad, 5.88–9.28 (M = 8.09) percent of the length of head. Two nostrils on ocular side, anterior nostril tubular, in front of lower edge of lower eye, posterior nostril simple, in the anterior half of interorbital space. Snout rather rounded, 34.26–37.10 (M = 36.02) percent of head, rostral hook short, extending to front of anterior nostril. Maxillary extending to behind fixed eye; angle of mouth extending below vertical from posterior half of fixed eye, nearer to tip of snout than to branchial opening; tip of snout to angle of mouth 44.33–50.0 (M = 46.69), angle of mouth to branchial opening 50.0–56.45 (M = 54.35) percent of length of head.

Scales: Ctenoid on ocular side, cycloid on blind side.

Lateral-Line System: Three lateral lines on ocular side, midlateral line with 110–138 (M = 120) scales, 20–25 (M = 23) scales between middle and upper lateral lines. No lateral line on blind side.

Interlinear scale rows 20 21 23 24 25

Frequencies 1 1 3 2 1

Fins: Dorsal with 124 rays, anal with 96 rays, caudal 10 in 1 specimen (radiograph).

Vertebrae: 55, comprising 11 abdominal and 44 caudal elements in 1 specimen (radiograph).

Coloration: Upper side uniformly brown, lower whitish in preserved specimens.

Size: Largest specimen examined, 566 (530 + 36) mm, is from Shanghai.

DISTRIBUTION.—China.

DIAGNOSIS AND
license
cc-by-nc-sa-3.0
bibliographic citation
Menon, A. G. K. 1977. "A systematic monograph of the tongue soles of the genus Cynoglossus Hamilton-Buchanan (Pisces, Cynoglossidae)." Smithsonian Contributions to Zoology. 1-129. https://doi.org/10.5479/si.00810282.238

Cynoglossus semilaevis

provided by wikipedia EN

Cynoglossus semilaevis, commonly known as the Chinese tongue sole, is a popular aquaculture flatfish species.[1] They are native to China's northern coast but have experienced overfishing these past three decades.[1][2] Tongue sole farming began in 2003 and they have since become a popular, expensive seafood.[2] However, tongue soles have created issues for farmers due to their pathogen susceptibility and uneven sex ratio.[2]

Sex determination

Sex & sex reversal

Cynoglossus semilaevis have a female heterogametic sex-determination system, with females being ZW and males being ZZ.[3] Female tongue soles grow up to 2-4 times larger and faster than males. As such, female tongue soles are preferred by farmers and attempts have been made to breed all-female stocks via artificial gynogenesis.[4] In both the wild and in aquaculture, the sex ratio of Cynoglossus semilaevis is male-skewed due to a number of the females becoming pseudomales.[5] Pseudomales have female ZW chromosomes, but become physiologically male.[6] The offspring of pseudomales have a significantly lower growth rate than the offspring of males, and are more likely to become pseudomales themselves, further skewing the sex ratio.[3][5] This change occurs due to a combination of genotypic sex determination and temperature-dependent sex determination.[7] Exposure to higher temperatures during the gonadal sex differentiation stage (~56–62 days post-hatching) makes the sex change more likely, with one study finding that the percentage of females who became pseudomales was increased to 73% when reared at a higher temperature (28°C) as opposed to a 14% sex-reversal rate when reared at an ambient temperature (22°C).[3][8] Furthermore, the offspring of the pseudomales reared at 28°C had a sex-reversal rate of 94% despite being reared at 22°C.[3] This high rate of females becoming pseudomales in the F2 generation was attributed to the offspring inheriting their Z chromosome from their pseudomale father and retaining paternal methylation patterns.[9]

Sex-specific molecular markers

A single SNP, Cyn_Z_6676874, allows certain females to become pseudomales.[10] Females with a thymine at this site can undergo sex reversal, but females with an adenine cannot.[10] There are also three known female-specific molecular markers that can be used to distinguish between the various tongue sole sexes.[5] Two SNPs, SNP_chr_8935925_C_T and SNP_chr_8936186_C_G, and one indel were found to enable accurate differentiation between males, females, and pseudomales.[5]

Gene expression in the gonads

Gene expression in the gonads of males and females are different before sex determination, after sex determination, and after exposure to higher temperatures.[11] Prior to sex determination, males and females have differentially expressed genes (DEGs) related to muscle development.[11] Following sex determination, females have upregulated female-specific genes, figla and foxl2, and downregulation of the male-specific genes, dmrt1 and amh, under both ambient and high-temperature conditions.[11] When exposed to higher temperatures, males, females, and pseudomales have hundreds of DEGs in common that are mainly involved in biological processes and molecular functions.[11]

Pseudomale gonads have more similar gene expression patterns to males than females.[7] DEGs between males and pseudomales played a role in spermatogenesis and energy metabolism.[11] Whereas, DEGS between females and pseudomales were related to steroid hormones, helicase activity, sexual differentiation, and development.[11]

References

  1. ^ a b Hu, Yuanri; Li, Yangzhen; Li, Zhongming; Chen, Changshan; Zang, Jiajian; Li, Yuwei; Kong, Xiangqing (December 2020). "Novel insights into the selective breeding for disease resistance to vibriosis by using natural outbreak survival data in Chinese tongue sole (Cynoglossus semilaevis)". Aquaculture. 529: 735670. doi:10.1016/j.aquaculture.2020.735670. S2CID 224900889.
  2. ^ a b c Li, Yangzhen; Hu, Yuanri; Yang, Yingming; Zheng, Weiwei; Chen, Changshan; Li, Zhongming (January 2021). "Selective breeding for juvenile survival in Chinese tongue sole (Cynoglossus semilaevis): Heritability and selection response". Aquaculture. 531: 735901. doi:10.1016/j.aquaculture.2020.735901. S2CID 224878642.
  3. ^ a b c d Shao, Changwei; Li, Qiye; Chen, Songlin; Zhang, Pei; Lian, Jinmin; Hu, Qiaomu; Sun, Bing; Jin, Lijun; Liu, Shanshan; Wang, Zongji; Zhao, Hongmei; Jin, Zonghui; Liang, Zhuo; Li, Yangzhen; Zheng, Qiumei (April 2014). "Epigenetic modification and inheritance in sexual reversal of fish". Genome Research. 24 (4): 604–615. doi:10.1101/gr.162172.113. ISSN 1088-9051. PMC 3975060. PMID 24487721.
  4. ^ Chen, Song-Lin; Tian, Yong-Sheng; Yang, Jing-Feng; Shao, Chang-Wei; Ji, Xiang-Shan; Zhai, Jie-Ming; Liao, Xiao-Lin; Zhuang, Zhi-Meng; Su, Peng-Zhi; Xu, Jian-Yong; Sha, Zhen-Xia; Wu, Peng-Fei; Wang, Na (April 2009). "Artificial Gynogenesis and Sex Determination in Half-Smooth Tongue Sole (Cynoglossus semilaevis)". Marine Biotechnology. 11 (2): 243–251. doi:10.1007/s10126-008-9139-0. ISSN 1436-2228. PMID 18779997. S2CID 24780167.
  5. ^ a b c d Zhang, Bo; Zhao, Na; Liu, Yangyang; Jia, Lei; Fu, Yan; He, Xiaoxu; Liu, Kefeng; Xu, Zijing; Bao, Baolong (November 2019). "Novel molecular markers for high-throughput sex characterization of Cynoglossus semilaevis". Aquaculture. 513: 734331. doi:10.1016/j.aquaculture.2019.734331. S2CID 199639905.
  6. ^ Dong, Zhongdian; Zhang, Ning; Liu, Yang; Xu, Wenteng; Cui, Zhongkai; Shao, Changwei; Chen, Songlin (January 2019). "Expression analysis and characterization of zglp1 in the Chinese tongue sole (Cynoglossus semilaevis)". Gene. 683: 72–79. doi:10.1016/j.gene.2018.10.003. PMID 30312653. S2CID 52975569.
  7. ^ a b Liu, Jinxiang; Liu, Xiaobing; Jin, Chaofan; Du, Xinxin; He, Yan; Zhang, Quanqi (29 May 2019). "Transcriptome Profiling Insights the Feature of Sex Reversal Induced by High Temperature in Tongue Sole Cynoglossus semilaevis". Frontiers in Genetics. 10: 522. doi:10.3389/fgene.2019.00522. ISSN 1664-8021. PMC 6548826. PMID 31191622.
  8. ^ Zhu, Ying; Hu, Qiaomu; Xu, Wenteng; Li, Hailong; Guo, Hua; Meng, Liang; Wei, Min; Lu, Sheng; Shao, Changwei; Wang, Na; Yang, Guanpin; Chen, Songlin (10 May 2017). Liu, Chunming (ed.). "Identification and analysis of the β-catenin1 gene in half-smooth tongue sole (Cynoglossus semilaevis)". PLOS ONE. 12 (5): e0176122. Bibcode:2017PLoSO..1276122Z. doi:10.1371/journal.pone.0176122. ISSN 1932-6203. PMC 5425175. PMID 28489928.
  9. ^ Chen, Songlin; Zhang, Guojie; Shao, Changwei; Huang, Quanfei; Liu, Geng; Zhang, Pei; Song, Wentao; An, Na; Chalopin, Domitille; Volff, Jean-Nicolas; Hong, Yunhan; Li, Qiye; Sha, Zhenxia; Zhou, Heling; Xie, Mingshu (March 2014). "Whole-genome sequence of a flatfish provides insights into ZW sex chromosome evolution and adaptation to a benthic lifestyle". Nature Genetics. 46 (3): 253–260. doi:10.1038/ng.2890. ISSN 1061-4036. PMID 24487278. S2CID 205348195.
  10. ^ a b Jiang, Li; Li, Hengde (1 February 2017). "Single Locus Maintains Large Variation of Sex Reversal in Half-Smooth Tongue Sole ( Cynoglossus semilaevis )". G3 Genes|Genomes|Genetics. 7 (2): 583–589. doi:10.1534/g3.116.036822. ISSN 2160-1836. PMC 5295603. PMID 28007836.
  11. ^ a b c d e f Wang, Qian; Liu, Kaiqiang; Feng, Bo; Zhang, Zhihua; Wang, Renkai; Tang, Lili; Li, Wensheng; Li, Qiye; Piferrer, Francesc; Shao, Changwei (22 November 2019). "Transcriptome of Gonads From High Temperature Induced Sex Reversal During Sex Determination and Differentiation in Chinese Tongue Sole, Cynoglossus semilaevis". Frontiers in Genetics. 10: 1128. doi:10.3389/fgene.2019.01128. ISSN 1664-8021. PMC 6882949. PMID 31824559.
license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN

Cynoglossus semilaevis: Brief Summary

provided by wikipedia EN

Cynoglossus semilaevis, commonly known as the Chinese tongue sole, is a popular aquaculture flatfish species. They are native to China's northern coast but have experienced overfishing these past three decades. Tongue sole farming began in 2003 and they have since become a popular, expensive seafood. However, tongue soles have created issues for farmers due to their pathogen susceptibility and uneven sex ratio.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN