Microdiversity Shapes the Seasonal Niche of Prokaryotic Plankton Inhabiting Surface Waters in a Coastal Upwelling System

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Cessna-Pamela Orta-Ponce, Rodrigo Alba-Salgueiro, Carlota Rodríguez, Joaquín Valencia-Vila, Pilar Díaz-Tapia, Antonio Bode, Mar Nieto-Cid, Marta M. Varela
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Abstract

Seasonality of prokaryotic abundance, diversity and community composition was investigated over a 2-year period in a coastal upwelling time-series station. A marked seasonality was found for prokaryotic abundance, peaking during upwelling and upwelling-to-downwelling transition, and decreasing during downwelling. The latter included a deeper mixed layer and a homogeneous water column favouring higher abundance of archaea (i.e., Marine Group II, Candiadatus nitrosopelagicus), SAR406 clade and the group Bacteria_Others including > 400 rare taxa. Upwelling and transition conditions, characterised by enhanced vertical stratification and a marked hydrographic variability, included a community less diverse with core-phylotypes proliferating, i.e., Flavobacteriaceae, Amylibacter and Planktomarina. Physical and biogeochemical variables collectively explained > 40% of the seasonal changes in prokaryotic assemblages. Additionally, fine-tune bacterial features evidenced ‘closely related taxa’ within particular bacterial phylotypes such as SAR116 clade; certain Flavobacteria belonging to NS2b, NS4 or NS9; members of the family Cryomorphaceae and Marine Group II, displaying seasonal microdiversity patterns. Taken together, seasonal hydrographic forcing induces a shift in the upwelling-driven microbiome providing new insights into the barely explored seasonal niche partitioning of surface prokaryotic communities in such highly productive upwelling systems. These results are of broad interest for understanding ecosystem functioning and forecast the impacts of current environmental change.

Abstract Image

微多样性塑造了居住在沿海上升流系统地表水中的原核浮游生物的季节生态位
对某沿海上升流时序站2年的原核生物丰度、多样性和群落组成进行了季节性研究。原核生物丰度具有明显的季节性,在上升流和上升流-下升流过渡期间达到峰值,在下升流期间下降。后者包括较深的混合层和均匀的水柱,有利于较高丰度的古细菌(即海洋II群,Candiadatus nitrosopelagicus), SAR406分支和细菌群(包括400个稀有分类群)。上升流和过渡条件以垂直分层增强和明显的水文变异性为特征,包括一个较少多样性的群落,即黄杆菌科,淀粉杆菌和浮游生物。物理和生物地球化学变量共同解释了原核生物组合中40%的季节变化。此外,微调细菌特征在特定的细菌类群(如SAR116枝)中证明了“密切相关的分类群”;某些黄杆菌属NS2b、NS4或NS9;冰苔科和海洋II组的成员,表现出季节性的微多样性模式。综上所述,季节性水文强迫导致了上升流驱动的微生物组的转变,为在这种高产的上升流系统中几乎没有被探索过的地表原核生物群落的季节性生态位划分提供了新的见解。这些结果对于理解生态系统功能和预测当前环境变化的影响具有广泛的意义。
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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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