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新热带地区安格兰亚科（万代兰族，兰科）及其最亲近的非洲近缘种的系统发育气候生态位保守性与气候适宜性演化

Phylogenetic climatic niche conservatism and evolution of climatic suitability in Neotropical Angraecinae (Vandeae, Orchidaceae) and their closest African relatives.

作者信息

Kolanowska Marta, Grochocka Elżbieta, Konowalik Kamil

机构信息

Department of Plant Taxonomy and Nature Conservation, University of Gdańsk, Gdańsk, Poland.

Department of Biodiversity Research, Global Change Research Institute AS CR, Brno, Czech Republic.

出版信息

PeerJ. 2017 May 16;5:e3328. doi: 10.7717/peerj.3328. eCollection 2017.

DOI:10.7717/peerj.3328
PMID:28533976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5436590/
Abstract

In the present study we investigate the concept of phylogenetic niche conservatism (PNC) within the American species of angraecoid orchids ( and ) and their closest relatives in the Old World () using ecological niche modelling (ENM). The predicted niche occupancy profiles were matched with the outcomes of previous phylogenetic studies to reconstruct the evolution of climatic suitability within the orchid group studied and evaluate the role of niche differentiation in the speciation of Angraecinae. No correlation between preferred niches and taxonomic relationships within the orchid group studied was revealed. The climatic suitability of the majority of the species overlapped each other, either fully or partially. This pattern is also present in the species of other orchid genera. Our research confirms a significant level of PNC in Orchidaceae, even within taxa exhibiting a transatlantic disjunction. The analysis of the evolution of climatic suitability indicated that the adaptation to various climatic conditions is not a factor that has driven speciation within orchids studied.

摘要

在本研究中，我们利用生态位建模（ENM），对美洲安格兰类兰花及其在旧世界的近缘种的系统发育生态位保守性（PNC）概念进行了研究。将预测的生态位占用概况与先前系统发育研究的结果相匹配，以重建所研究兰花类群内气候适宜性的演变，并评估生态位分化在安格兰亚科物种形成中的作用。在所研究的兰花类群中，未发现首选生态位与分类关系之间存在相关性。大多数物种的气候适宜性彼此完全或部分重叠。这种模式在其他兰花属的物种中也存在。我们的研究证实了兰科中存在显著水平的PNC，即使在表现出跨大西洋间断分布的类群中也是如此。对气候适宜性演变的分析表明，对各种气候条件的适应并不是所研究兰花物种形成的驱动因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/18822add2619/peerj-05-3328-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/6a1fe9d57d9a/peerj-05-3328-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/ce64f2626b91/peerj-05-3328-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/e5d51038bd16/peerj-05-3328-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/344a7ed90702/peerj-05-3328-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/3a11f9faf136/peerj-05-3328-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/9504dfc25ee5/peerj-05-3328-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/14b120c3dca7/peerj-05-3328-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/18822add2619/peerj-05-3328-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/6a1fe9d57d9a/peerj-05-3328-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/ce64f2626b91/peerj-05-3328-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/e5d51038bd16/peerj-05-3328-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/344a7ed90702/peerj-05-3328-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/3a11f9faf136/peerj-05-3328-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/9504dfc25ee5/peerj-05-3328-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/14b120c3dca7/peerj-05-3328-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c7/5436590/18822add2619/peerj-05-3328-g008.jpg

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