Literature DB >> 27662109

Modified niche optima and breadths explain the historical contingency of bacterial community responses to eutrophication in coastal sediments.

S Fodelianakis1,2, A Moustakas3, N Papageorgiou2, O Manoli2, I Tsikopoulou2, G Michoud1, D Daffonchio1, I Karakassis2, E D Ladoukakis2.   

Abstract

Previous studies have shown that the response of bacterial communities to disturbances depends on their environmental history. Historically fluctuating habitats host communities that respond better to disturbance than communities of historically stable habitats. However, the exact ecological mechanism that drives this dependency remains unknown. Here, we experimentally demonstrate that modifications of niche optima and niche breadths of the community members are driving this dependency of bacterial responses to past environmental conditions. First, we develop a novel, simple method to calculate the niche optima and breadths of bacterial taxa regarding single environmental gradients. Then, we test this method on sediment bacterial communities of three habitats, one historically stable and less loaded and two historically more variable and more loaded habitats in terms of historical chlorophyll-α water concentration, that we subject to hypoxia via organic matter addition ex situ. We find that communities containing bacterial taxa differently adapted to hypoxia show different structural and functional responses, depending on the sediment's environmental history. Specifically, in the historically less fluctuating and loaded sediments where we find more taxa poorly adapted to hypoxic conditions, communities change a lot over time and organic matter is not degraded efficiently. The opposite is true for the historically more fluctuating and loaded sediments where we find more taxa well adapted to hypoxia. Based on the community responses observed here, we also propose an alternative calculation of community resistance that takes into account how rapidly the communities respond to disturbances and not just the initial and final states of the community.
© 2016 The Authors. Molecular Ecology Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  adaptation; bacterial communities; community resistance; disturbance; environmental history

Mesh:

Year:  2016        PMID: 27662109     DOI: 10.1111/mec.13842

Source DB:  PubMed          Journal:  Mol Ecol        ISSN: 0962-1083            Impact factor:   6.185


  4 in total

1.  Assembly mechanisms of soil bacterial communities in subalpine coniferous forests on the Loess Plateau, China.

Authors:  Pengyu Zhao; Jinxian Liu; Tong Jia; Zhengming Luo; Cui Li; Baofeng Chai
Journal:  J Microbiol       Date:  2019-05-27       Impact factor: 3.422

2.  Dispersal homogenizes communities via immigration even at low rates in a simplified synthetic bacterial metacommunity.

Authors:  Stilianos Fodelianakis; Alexander Lorz; Adriana Valenzuela-Cuevas; Alan Barozzi; Jenny Marie Booth; Daniele Daffonchio
Journal:  Nat Commun       Date:  2019-03-21       Impact factor: 14.919

3.  Discovery of Afifi, the shallowest and southernmost brine pool reported in the Red Sea.

Authors:  Carlos M Duarte; Anders Røstad; Grégoire Michoud; Alan Barozzi; Giuseppe Merlino; Antonio Delgado-Huertas; Brian C Hession; Francis L Mallon; Abdulakader M Afifi; Daniele Daffonchio
Journal:  Sci Rep       Date:  2020-01-22       Impact factor: 4.379

4.  Microdiversity characterizes prevalent phylogenetic clades in the glacier-fed stream microbiome.

Authors:  Stilianos Fodelianakis; Alex D Washburne; Massimo Bourquin; Paraskevi Pramateftaki; Tyler J Kohler; Michail Styllas; Matteo Tolosano; Vincent De Staercke; Martina Schön; Susheel Bhanu Busi; Jade Brandani; Paul Wilmes; Hannes Peter; Tom J Battin
Journal:  ISME J       Date:  2021-09-15       Impact factor: 10.302

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.