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博碩士論文 etd-0715118-104225 詳細資訊
Title page for etd-0715118-104225
論文名稱
Title
南中國海花身鯻 (Terapon jarbua) 之族群連通性
Population connectivity of Terapon jarbua (Pisces: Perciformes) in the South China Sea
系所名稱
Department
畢業學年期
Year, semester
語文別
Language
學位類別
Degree
頁數
Number of pages
63
研究生
Author
指導教授
Advisor
召集委員
Convenor
口試委員
Advisory Committee
口試日期
Date of Exam
2017-07-27
繳交日期
Date of Submission
2018-08-15
關鍵字
Keywords
南中國海、族群連通性、cytochrome b、COI、花身鯻(Terapon jarbua)
cytochrome b, COI, population community, the South China Sea, Terapon jarbua
統計
Statistics
本論文已被瀏覽 5868 次,被下載 66
The thesis/dissertation has been browsed 5868 times, has been downloaded 66 times.
中文摘要
目前於南中國海的族群遺傳學研究,都傾向於遷徙能力良好的大型經濟魚類或是浮游期偏長的魚種,其結果也幾乎沒有明顯的分化。本研究選用浮游期偏短且體型偏小的花身鯻(Terapon jarbua)作為研究物種,採集環繞整個南中國海的12個樣點,包含高雄、東沙、太平島、饒平、香港、馬來西亞的關丹與古晉、菲律賓的宿霧與阿拉米諾斯、柬埔寨的西哈努克以及越南的寧順與海防,分析其族群聯通性,以探討其於南中國海的遺傳結構與洋流的關係。利用180尾花身鯻樣本的COI以及cyt b共1752鹼基對建構之Maximum likelihood tree與median-joining network顯示所有的單倍型能被分為兩大譜系(A與B),此外譜系A又能細分成兩個亞譜系(1與2),其中譜系B與亞譜系1皆僅包含古晉的個體,亞譜系2則包含來自所有樣點的個體。以條紋鯻(學明)為參考的遺傳距離顯示,兩譜系間可能仍不足以被定義為隱蔽種。此外,本研究將部份前人於印度太平洋地區研究的COI序列下載後,與我們的數據利用median-joining network重新分析,發現本研究的亞譜系2與其太平洋群相等,亞譜系1與其印度洋群相等,古晉特有的譜系B也未出現於前人的研究中。另一方面,本研究未採得任何前人的東非群個體。FST值顯示關丹和古晉與其他地區分別有較弱與極高的遺傳分化,其它族群間則未有顯著差異。Barrier分析顯示有一道較強的遺傳屏障圍繞古晉,另一道較弱的則位於南中國海中部,AMOVA以Barrier作為分組依據,支持古晉與其他地區巨大的遺傳差異。在歷史族群動態分析方面,Tajima’s D, Fu’s Fs, mismatch distribution, Goodness-of-fit test, demographic expansion parameters以及Bayesian Skyline plot都顯示譜系A過去有一個明顯的族群突然擴張(四萬到一萬年前),譜系B則是一個相對較弱的擴張或是穩定的成長。根據maximum credibility tree,花身鯻譜系的分化時間大致位於更新世中期到晚期之間。
Abstract
Most studies on the genetic structure of fishes in the South China Sea (SCS) showed weak genetic structure probably due to long pelagic larval duration (PLD) and long-distance migration of large size species. In this study, Terapon jarbua, a small size fish with a shorter PLD, was selected as our target species, collected from 12 sampling sites along the SCS, including Kaohsiung, Dongsha Atoll, Taiping Island, Raoping, Hong Kong, Hai Phong and Ninh Thuan of Vietnam, Sihanoukville of Cambodia, Kuantan and Kuching of Malaysia and Cebu and Alaminos of the Philippines. In this research, population connectivity of T. jarbua is studied in order to evaluate the influence of currents on its population genetic structure. Fragments of cyt b and COI (1752 bps) of 180 specimens of T. jarbua were sequenced to study their relationships among populations. Maximum likelihood tree and median-joining network showed that all haplotypes were divided into two lineages (A and B), and lineage A was further divided into two sublineages (1 and 2). Among the divisions, lineage B and sublineage 1 comprised individuals exclusively from Kuching while sublineage 2 contained individuals from all sampling sites. Interspecific genetic distance based on the comparison to T. theraps suggests that cryptic species may not be an issue in these two lineages. In addition to our own data, COI sequences from previous study were downloaded from GenBank to reconstruct the network. The median-joining network is divided into four groups, in which sublineage 2 of the present study fell into Pacific group of previous study, and sublineage 1 was identical to their Indian group. On the other hand, no haplotype of Iles Eparses group is collected in the SCS and lineage B that is exclusively from Kuching is not present in the previous study. FST values and Barrier analysis showed that gene flows between Malaysian water and other sites were at least partially limited, and a strong genetic barrier separated Kuching from all other locations while a weaker barrier located in the middle of the SCS. Based on the results from Barrier, AMOVA analysis showed that the genetic structure of Kuching was significant. Tajima’s D, Fu’s Fs, mismatch distribution, Goodness-of-fit test, demographic expansion parameters and Bayesian Skyline plot all suggested that lineage A experience a demographic expansion (0.04~0.01 Ma), and the expansion of lineage B would be much smaller or lineage B has undergone a stable growth. According to maximum credibility tree, most of the divergence time for T. jarbua corresponded to the middle to late Pleistocene.
目次 Table of Contents
學位論文審定書..........................................................................i
謝辭..............................................................................................ii
摘要.............................................................................................iii
Abstract .......................................................................................iv
Content........................................................................................vi
Figure content ...........................................................................viii
Table content...............................................................................ix
Introduction.................................................................................. 1
Introduction to Terapon jarbua ............................................................................................. 1
Phylogeography ..................................................................................................................... 2
The types of molecular markers and applications ................................................................. 3
How current and vicariance affect the genetic structure of fish ............................................ 4
Previous studies about the genetic structure of fishes in the SCS ......................................... 8
Materials and Methods .............................................................. 11
Sample collection, DNA extraction and PCR ..................................................................... 11
Electrophoresis, sequencing and alignment ........................................................................ 13
Genealogy reconstruction, genetic diversity and interspecific genetic distance ................. 14
Population structure ............................................................................................................. 15
Historical demographic analysis .......................................................................................... 16
Divergence time estimation ................................................................................................. 19
Results........................................................................................ 20
Genetic composition and diversity ...................................................................................... 20
Genealogy reconstruction and interspecific genetic distance .............................................. 20
Population structure ............................................................................................................. 22
Historical demographic analysis .......................................................................................... 23
Divergence time estimation ................................................................................................. 24
Discussion.................................................................................. 25
Genetic diversity .................................................................................................................. 25
Population genetic structure ................................................................................................ 26
Historical demographic analysis and divergence time estimation ....................................... 29
References.................................................................................. 31
Tables ......................................................................................... 43
Figures........................................................................................ 47
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