• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

形态学和分子证据支持潮间带藤壶Nilsson-Cantell，1921年（龟藤壶目，小藤壶科）为印度-太平洋海域的一个有效物种。

Morphological and molecular evidence support the intertidal barnacle Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters.

作者信息

Chan Benny K K, Tsao Yao Feng, Ganmanee Monthon

机构信息

Biodiversity Research Center, Academia Sinica, Taipei 115, Taiwan Biodiversity Research Center, Academia Sinica Taipei Taiwan.

Faculty of Agricultural Technology, King Mongkut's Institute of Technology Ladkrabang, Chalongkrung Road, Ladkrabang, Bangkok 10520, Thailand King Mongkut's Institute of Technology Bangkok Thailand.

出版信息

Zookeys. 2020 Feb 20;914:1-31. doi: 10.3897/zookeys.914.49328. eCollection 2020.

DOI:10.3897/zookeys.914.49328
PMID:32132853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7046729/
Abstract

is a chthamalid intertidal barnacle with eight shell plates. There are currently two species of such barnacles: Darwin, 1854 (type locality in the Philippines), common in the Indo-Pacific region, and Sowerby, 1825, only recorded in South Africa. Nilsson-Cantell, 1921, identified from the Mergui Archipelago in Myanmar, was considered to be conspecific with by Hiro (1939) based on samples collected in Taiwan. The morphological differences in shell and opercular plates between and are believed to be intra-specific variations due to different degrees of shell erosion. In the present study, the genetic and morphological differentiations of in the Indo-Pacific region were examined. This study found two molecular clades (with inter-specific differences) based on the divergence in the COI genes, and the species also have distinct geographical distributions. The clade covers samples collected from the Philippines and Taiwan waters and the other clade, which we argue is , is distributed in Phuket and Krabi, Thailand and Langkawi, Malaysia. Phuket and Krabi are located approximately 300 km south of the Mergui Archipelago, the type locality of . The morphology of samples collected from Thailand fits the type description of in Nilsson-Cantell (1921). Our study concludes that is a valid species based on morphological and molecular evidence.

摘要

是一种具有八块壳板的潮间带藤壶。目前有两种这样的藤壶：达尔文藤壶，1854年（模式产地在菲律宾），在印度-太平洋地区很常见；以及索尔比藤壶，1825年，仅在南非有记录。1921年的尼尔森-坎特尔藤壶，从缅甸的丹老群岛鉴定而来，根据在台湾采集的样本，广（1939年）认为它与达尔文藤壶同种。达尔文藤壶和尼尔森-坎特尔藤壶在壳和盖板上的形态差异被认为是由于壳侵蚀程度不同导致的种内变异。在本研究中，对印度-太平洋地区的尼尔森-坎特尔藤壶的遗传和形态分化进行了研究。基于细胞色素氧化酶亚基I（COI）基因的差异，本研究发现了两个分子分支（存在种间差异），并且这些物种也有不同的地理分布。达尔文藤壶分支涵盖了从菲律宾和台湾海域采集的样本，另一个分支，我们认为是尼尔森-坎特尔藤壶，分布在泰国的普吉岛和甲米以及马来西亚的兰卡威。普吉岛和甲米位于丹老群岛模式产地以南约300公里处。从泰国采集的样本形态符合尼尔森-坎特尔（1921年）对尼尔森-坎特尔藤壶的类型描述。我们的研究基于形态和分子证据得出结论，尼尔森-坎特尔藤壶是一个有效物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/35eafd31e989/zookeys-914-001-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/84cf6f1f5260/zookeys-914-001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/e004168caba5/zookeys-914-001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/0660dfa03dfc/zookeys-914-001-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/65e7f43f81b3/zookeys-914-001-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/3efc59a744b3/zookeys-914-001-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/7bf5de4fe4aa/zookeys-914-001-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/d15376243b68/zookeys-914-001-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/5c0f9e7fd45e/zookeys-914-001-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/98c120c42bbd/zookeys-914-001-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/1c3840e71eb0/zookeys-914-001-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/0f6dd3867d2c/zookeys-914-001-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/67b0ba08d5e6/zookeys-914-001-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/b409c1cbe9ac/zookeys-914-001-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/50b1e4932bc4/zookeys-914-001-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/36366a652116/zookeys-914-001-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/501a6bfccfbf/zookeys-914-001-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/4ae152513b78/zookeys-914-001-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/35eafd31e989/zookeys-914-001-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/84cf6f1f5260/zookeys-914-001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/e004168caba5/zookeys-914-001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/0660dfa03dfc/zookeys-914-001-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/65e7f43f81b3/zookeys-914-001-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/3efc59a744b3/zookeys-914-001-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/7bf5de4fe4aa/zookeys-914-001-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/d15376243b68/zookeys-914-001-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/5c0f9e7fd45e/zookeys-914-001-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/98c120c42bbd/zookeys-914-001-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/1c3840e71eb0/zookeys-914-001-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/0f6dd3867d2c/zookeys-914-001-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/67b0ba08d5e6/zookeys-914-001-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/b409c1cbe9ac/zookeys-914-001-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/50b1e4932bc4/zookeys-914-001-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/36366a652116/zookeys-914-001-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/501a6bfccfbf/zookeys-914-001-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/4ae152513b78/zookeys-914-001-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29a/7046729/35eafd31e989/zookeys-914-001-g018.jpg

相似文献

1
Morphological and molecular evidence support the intertidal barnacle Nilsson-Cantell, 1921 (Thoracica, Chthamalidae) as a valid species in Indo-Pacific waters.形态学和分子证据支持潮间带藤壶Nilsson-Cantell，1921年（龟藤壶目，小藤壶科）为印度-太平洋海域的一个有效物种。
Zookeys. 2020 Feb 20;914:1-31. doi: 10.3897/zookeys.914.49328. eCollection 2020.
2
Genetic and morphological differentiation of the Indo-West Pacific intertidal barnacle Chthamalus malayensis.印太浅海藤壶 Chthamalus malayensis 的遗传和形态分化。
Integr Comp Biol. 2012 Sep;52(3):388-409. doi: 10.1093/icb/ics044. Epub 2012 Apr 20.
3
Diversity of intertidal, epibiotic, and fouling barnacles (Cirripedia, Thoracica) from Gujarat, northwest India.来自印度西北部古吉拉特邦的潮间带、体表共生和污损藤壶（蔓足亚纲，围胸目）的多样性。
Zookeys. 2021 Mar 25;1026:143-178. doi: 10.3897/zookeys.1026.60733. eCollection 2021.
4
Perreault, 2014 or (Anderson, 1992)? A new coral-associated barnacle sharing characteristics of these two genera in Pacific waters (Crustacea, Cirripedia, Thoracica, Pyrgomatidae).佩罗，2014年 还是 （安德森，1992年）？太平洋海域一种具有这两个属特征的新的珊瑚共生藤壶（甲壳纲，蔓足亚纲，围胸目，笠藤壶科）。
Zookeys. 2017 Dec 7(719):1-22. doi: 10.3897/zookeys.719.12471. eCollection 2017.
5
Maternal inheritance of F1 hybrid morphology and colony shape in the coral genus .珊瑚属中F1杂交形态和群体形状的母系遗传
PeerJ. 2019 Feb 19;7:e6429. doi: 10.7717/peerj.6429. eCollection 2019.
6
DNA-based diversity assessment reveals a new coral barnacle, sp. nov. (Balanomorpha: Pyrgomatidae) exclusively associated with the high latitude coral in the waters of southern Korea.基于DNA的多样性评估揭示了一种新的珊瑚藤壶，新物种（龟藤壶科：笠藤壶亚科）仅与韩国南部水域的高纬度珊瑚相关联。
PeerJ. 2021 Apr 29;9:e11284. doi: 10.7717/peerj.11284. eCollection 2021.
7
Erratum: Eyestalk Ablation to Increase Ovarian Maturation in Mud Crabs.勘误：切除眼柄以增加泥蟹的卵巢成熟度。
J Vis Exp. 2023 May 26(195). doi: 10.3791/6561.
8
Zoogeography of intertidal communities in the West Indian Ocean as determined by ocean circulation systems: patterns from the Tetraclita barnacles.西印度洋潮间带生物地理分布由海洋环流系统决定：藤壶属的模式。
PLoS One. 2012;7(9):e45120. doi: 10.1371/journal.pone.0045120. Epub 2012 Sep 14.
9
Unraveling cryptic diversity among shallow-water tonguefishes (Pleuronectiformes: Cynoglossidae: Symphurus) from the Indo-West Pacific region, with descriptions of five new species.揭开印度洋-西太平洋地区浅海舌鳎（鲽形目：舌鳎科：舌鳎属）神秘多样之谜，描述五个新种。
Zootaxa. 2021 Sep 14;5039(1):1-55. doi: 10.11646/zootaxa.5039.1.1.
10
Descriptions of four new sponge-inhabiting barnacles (Thoracica: Archaeobalanidae: Acastinae).四种新的栖息于海绵的藤壶（围胸目：古藤壶科：阿卡斯藤壶亚科）的描述。
Zootaxa. 2017 Jun 16;4277(2):151-198. doi: 10.11646/zootaxa.4277.2.1.

本文引用的文献

1
Complete mitochondrial genome of the catophragmid barnacle (Cirripedia, Thoracica, Balanomorpha, Catophragmidae).猫茗荷藤壶（蔓足亚纲、围胸目、藤壶亚目、猫茗荷科）的完整线粒体基因组
Mitochondrial DNA B Resour. 2018 Oct 26;3(2):1286-1287. doi: 10.1080/23802359.2018.1532843.
2
Discovery of (Darwin) and Chan & Cheang (Balanomorpha, Tetraclitidae) from the Andaman Sea, eastern Indian Ocean.在印度洋东部安达曼海发现（达尔文）以及陈和张（笠藤壶科，龟甲藤壶属）。
Zookeys. 2019 Mar 25;833:1-20. doi: 10.3897/zookeys.833.30689. eCollection 2019.
3
MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms.
MEGA X：跨越计算平台的分子进化遗传学分析。
Mol Biol Evol. 2018 Jun 1;35(6):1547-1549. doi: 10.1093/molbev/msy096.
4
UFBoot2: Improving the Ultrafast Bootstrap Approximation.UFBoot2：改进超快bootstrap 逼近算法。
Mol Biol Evol. 2018 Feb 1;35(2):518-522. doi: 10.1093/molbev/msx281.
5
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP.系统发育树的置信区间：一种使用自展法的方法。
Evolution. 1985 Jul;39(4):783-791. doi: 10.1111/j.1558-5646.1985.tb00420.x.
6
ModelFinder: fast model selection for accurate phylogenetic estimates.ModelFinder：用于准确系统发育估计的快速模型选择
Nat Methods. 2017 Jun;14(6):587-589. doi: 10.1038/nmeth.4285. Epub 2017 May 8.
7
W-IQ-TREE: a fast online phylogenetic tool for maximum likelihood analysis.W-IQ-TREE：一种用于最大似然分析的快速在线系统发育工具。
Nucleic Acids Res. 2016 Jul 8;44(W1):W232-5. doi: 10.1093/nar/gkw256. Epub 2016 Apr 15.
8
IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies.IQ-TREE：一种用于估计最大似然系统发育树的快速且有效的随机算法。
Mol Biol Evol. 2015 Jan;32(1):268-74. doi: 10.1093/molbev/msu300. Epub 2014 Nov 3.
9
Mitochondrial evolution across lineages of the vampire barnacle Notochthamalus scabrosus.吸血藤壶Notochthamalus scabrosus各谱系的线粒体进化
Mitochondrial DNA. 2015 Feb;26(1):7-10. doi: 10.3109/19401736.2013.825791. Epub 2013 Sep 19.
10
Australian barnacles (Cirripedia: Thoracica), distributions and biogeographical affinities.澳大利亚藤壶（甲壳纲：Thoracica）的分布与生物地理亲缘关系。
Integr Comp Biol. 2012 Sep;52(3):366-87. doi: 10.1093/icb/ics100.