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uBio  Web  Results 21 - 30 of about 1626 Scientific:    Cephalopholis hemistiktos (duskyfin grouper)  Synonyms:    Anyperodon leucogrammicus (White-lined rockcod)     Cephalopholis hemistiktos (yellowfin hind)     Epinephelus corallicola (Coral grouper)     Epinephelus howlandi (blacksaddle grouper)     Serranus corallicola     Serranus hemistiktos  Broader Terms:    Cephalopholis     Epinephelus (groupers)     Perciformes (perch-likes)     Serranus     duskyfin      Latest Articles on duskyfin grouper from uBioRSS Serranus hemistictus Rüppell, 1830 - WoRMS latest edits Levels and distribution of organophosphorus flame retardants and plasticize... - ScienceDirect Search: species External Resources: 21.  Antibiotics in marine aquaculture farms surrounding Laizhou Bay, Bohai Sea: Distribution characteristics considering various culture modes and organism species. Han QF, Zhang XR, Xu XY, Wang XL, Yuan XZ, Ding ZJ, Zhao S, Wang SG The Science of the total environment, 2021 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 22.  Characterization of viral insulins reveals white adipose tissue-specific effects in mice. Chrudinová M, Moreau F, Noh HL, Páníková T, ?áková L, Friedline RH, Valenzuela FA, Kim JK, Jirá?ek J, Kahn CR, Altindis E Molecular metabolism, 2021 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 23.  E3 Ubiquitin Ligase RNF114 Inhibits Innate Immune Response to Red-Spotted Grouper Nervous Necrosis Virus Infection in Sea Perch by Targeting MAVS and TRAF3 to Mediate Their Degradation. Xiang Y, Zhang W, Jia P, Lu X, Liu W, Yi M, Jia K Journal of immunology (Baltimore, Md. : 1950), 2021 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 24.  Zschokkella epinepheli n. sp. (Myxosporea: Myxidiidae) infecting the gallbladder of the white grouper Epinephelus aeneus (Serranidae) from Tunisian waters. Bouderbala K, Rangel LF, Santos MJ, Bahri S Parasitology research, 2021 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 25.  Physical interactions facilitate sex change in the protogynous orange-spotted grouper, Epinephelus coioides. Chen J, Peng C, Huang J, Shi H, Xiao L, Tang L, Lin H, Li S, Zhang Y Journal of fish biology J Fish Biol Physical interactions facilitate sex change in the protogynous orange-spotted grouper, Epinephelus coioides. 10.1111/jfb.14663 Sex change in teleost fishes is commonly regulated by social factors. In species that exhibit protogynous sex change, such as the orange-spotted grouper Epinephelus coioides, when the dominant males are removed from the social group, the most dominant female initiates sex change. The aim of this study was to determine the regulatory mechanisms of socially controlled sex change in E. coioides. We investigated the seasonal variation in social behaviours and sex change throughout the reproductive cycle of E. coioides, and defined the behaviour pattern of this fish during the establishment of a dominance hierarchy. The social behaviours and sex change in this fish were affected by season, and only occurred during the prebreeding season and breeding season. Therefore, a series of sensory isolation experiments was conducted during the breeding season to determine the role of physical, visual and olfactory cues in mediating socially controlled sex change. The results demonstrated that physical interactions between individuals in the social groups were crucial for the initiation and completion of sex change, whereas visual and olfactory cues alone were insufficient in stimulating sex change in dominant females. In addition, we propose that the steroid hormones 11-ketotestosterone and cortisol are involved in regulating the initiation of socially controlled sex change. © 2020 Fisheries Society of the British Isles. Chen Jiaxing J Southern Marine Science and Engineering Guangdong Laboratory, Zhanjiang, China. State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory for Aquatic Economic Animals and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), School of Life Sciences, Sun Yat-Sen University, Guangzhou, China. Peng Cheng C Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Guangdong Public Laboratory of Wild Animal Conservation and Utilization, Guangdong Institute of Applied Biological Resources, Guangzhou, China. Huang Jingjun J College of Life Sciences, Southwest Forestry University, Kunming, China. Shi Herong H Marine Fisheries Development Center of Guangdong Province, Huizhou, China. Xiao Ling L State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory for Aquatic Economic Animals and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), School of Life Sciences, Sun Yat-Sen University, Guangzhou, China. Tang Lin L State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory for Aquatic Economic Animals and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), School of Life Sciences, Sun Yat-Sen University, Guangzhou, China. Lin Haoran H State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory for Aquatic Economic Animals and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), School of Life Sciences, Sun Yat-Sen University, Guangzhou, China. Li Shuisheng S Southern Marine Science and Engineering Guangdong Laboratory, Zhanjiang, China. State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory for Aquatic Economic Animals and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), School of Life Sciences, Sun Yat-Sen University, Guangzhou, China. Zhang Yong Y https://orcid.org/0000-0002-8709-0138 Southern Marine Science and Engineering Guangdong Laboratory, Zhanjiang, China. State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory for Aquatic Economic Animals and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), School of Life Sciences, Sun Yat-Sen University, Guangzhou, China. Marine Fisheries Development Center of Guangdong Province, Huizhou, China. eng This work was supported by the National Natural Science Foundation of China (31972769, 31902346, 31802274), the Guangdong Provincial Natural Science Foundation (2018A030313890, 2018B030311026), the Guangdong Provincial Special Fund For Modern Agriculture Industry Technology Innovation Teams (2019KJ143), the GDAS Special Project of Science and Technology Development (2019GDASYL-0103065), the Science and Technology Planning Project of Huizhou (20170214023102296), the Special Fund of State Key Laboratory of Developmental Biology of Freshwater (2018KF001) and the Open Fund of Guangdong South China Sea Key Laboratory of Aquaculture for Aquatic Economic Animals (KFKT2019ZD07). Journal Article 2020 12 30 England J Fish Biol 0214055 0022-1112 IM dominance hierarchy physical interaction season sensory isolation sex change 2020 04 16 2020 12 15 2020 12 29 2020 12 31 6 0 2020 12 31 6 0 2020 12 30 8 36 aheadofprint 33377528 10.1111/jfb.14663