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生活在潮间带:干燥和遮荫会降低海草生长,但高盐度或来源种群没有额外影响。

Living in the intertidal: desiccation and shading reduce seagrass growth, but high salinity or population of origin have no additional effect.

作者信息

Suykerbuyk Wouter, Govers Laura L, van Oven W G, Giesen Kris, Giesen Wim B J T, de Jong Dick J, Bouma Tjeerd J, van Katwijk Marieke M

机构信息

Department of Estuarine and Delta Systems, and Utrecht University, Royal Netherlands Institute for Sea Research (NIOZ), Yerseke, Netherlands.

Department of Environmental Science, Institute for Water and Wetland Research, Radboud University Nijmegen, Nijmegen, Netherlands.

出版信息

PeerJ. 2018 Jul 20;6:e5234. doi: 10.7717/peerj.5234. eCollection 2018.

DOI:10.7717/peerj.5234
PMID:30042889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6055680/
Abstract

The limiting effects of stressors like desiccation, light and salinity on seagrass growth and distribution are well-studied. However, little is known about their interactive effects, and whether such effects might differ among populations that are adapted to different local conditions. In two laboratory experiments we tested (a) if growth and development of intertidal, temperate is affected by emergence time (experiment 1 and 2), and (b) how this is affected by an additional, second stressor, namely shading (experiment 1) or high salinity (25, 30 and 35, experiment 2). In addition, we tested (c) whether the effects of emergence time and salinity varied between three different European seagrass populations (Saint-Jacut/France, Oosterschelde/The Netherlands, and Sylt/Germany), which are likely adapted to different salinity levels (experiment 2). In both experiments, emergence of 8 h per tidal cycle (of 12 h) had a negative effect on seagrass relative growth rate (RGR), and aboveground biomass. Emergence furthermore reduced either rhizome length (experiment 1) or belowground biomass (experiment 2). Shading (experiment 1) resulted in lower RGR and a two-fold higher aboveground/belowground ratio. We found no interactive effects of emergence and shading stress. Salinity (experiment 2) did not affect seagrass growth or morphology of any of the three populations. The three tested populations differed greatly in morphology but showed no differential response to emergence or salinity level (experiment 2). Our results indicate that emergence time and shading show an additive negative effect (no synergistic or antagonistic effect), making the plants still vulnerable to such combination, a combination that may occur as a consequence of self-shading during emergence or resulting from algal cover. Emergence time likely determines the upper limit of and such shading will likely lower the upper limit. Shading resulted in higher aboveground/belowground ratios as is a general response in seagrass. of different populations originating from salinity 30 and 35 seem tolerant to variations in salinity within the tested range. Our results indicate that the three tested populations show morphotypic rather than ecotypic variation, at least regarding the salinity and emergence, as there were no interactive effects with origin. For restoration, this implies that the salinity regime of the donor and receptor site of is of no concern within the salinity range 25-35.

摘要

脱水、光照和盐度等应激源对海草生长和分布的限制作用已得到充分研究。然而,对于它们的交互作用,以及这些作用在适应不同当地条件的种群之间是否存在差异,人们却知之甚少。在两项实验室实验中,我们测试了:(a)潮间带温带海草的生长和发育是否受出露时间影响(实验1和2),以及(b)这如何受到另一种第二应激源的影响,即遮荫(实验1)或高盐度(25、30和35,实验2)。此外,我们测试了(c)出露时间和盐度的影响在三个不同的欧洲海草种群(法国圣雅屈、荷兰奥斯坦德和德国叙尔特)之间是否存在差异,这些种群可能适应不同的盐度水平(实验2)。在两项实验中,每个潮汐周期(12小时)出露8小时对海草相对生长率(RGR)和地上生物量都有负面影响。出露还会减少根状茎长度(实验1)或地下生物量(实验2)。遮荫(实验1)导致较低的RGR和地上/地下比提高两倍。我们未发现出露和遮荫应激的交互作用。盐度(实验2)对三个种群中任何一个的海草生长或形态均无影响。所测试的三个种群在形态上差异很大,但对出露或盐度水平均未表现出差异响应(实验2)。我们的结果表明,出露时间和遮荫表现出累加的负面影响(无协同或拮抗作用),这使得植物仍然易受这种组合的影响,这种组合可能是出露期间自我遮荫的结果,或是藻类覆盖造成的。出露时间可能决定了海草生长的上限,而这种遮荫可能会降低上限。遮荫导致地上/地下比升高,这是海草的一般响应。源自盐度30和35的不同种群似乎能够耐受测试范围内的盐度变化。我们的结果表明,至少在盐度和出露方面,所测试的三个种群表现出形态型而非生态型变异,因为不存在与种群来源的交互作用。对于恢复而言,这意味着在25 - 35的盐度范围内,海草供体和受体地点的盐度状况无需考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/0c4c5c28e6b0/peerj-06-5234-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/9a7f186425e4/peerj-06-5234-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/69877f73e0b8/peerj-06-5234-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/ad5770128dd7/peerj-06-5234-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/0c4c5c28e6b0/peerj-06-5234-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/9a7f186425e4/peerj-06-5234-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/69877f73e0b8/peerj-06-5234-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/ad5770128dd7/peerj-06-5234-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e2/6055680/0c4c5c28e6b0/peerj-06-5234-g004.jpg

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