María Froján, Marta Muñoz-Colmenero, Isabel G. Teixeira, Belén Arbones, Carmen G. Sotelo, Begoña Correa, Francisco G. Figueiras, Carmen G. Castro
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引用次数: 0
摘要
几十年来,由于其体积小,鉴定微真核和纳米真核浮游生物一直具有挑战性,与较大的浮游生物相比,我们对其组成和动力学的了解存在重大差距。分子技术的出现为探索这种隐藏的多样性打开了新的可能性。我们利用元条形码技术,针对18S rDNA的V9区域,识别了Ría de Vigo在上升流季节的微真核和纳米真核生物的主要分类群。纳米真核生物(NE)比微真核生物(PE)表现出更大的多样性。具体而言,NE主要由纳米硅藻和鞭毛藻组成,其中许多是未分类的新种。在PE中,Syndiniales和Marine Stramenopiles (MAST)是鉴定的主要成分。我们还捕获了PE和NE的生物量和组成的短期变化,其中平流成为最重要的驱动因素之一。最值得注意的是未分配的微真核生物流入Ría,可能是由下行期间的负循环驱动的。此外,Ría内的局部放牧似乎足够重要,足以改变NE动态,但对PE的影响很小。我们的发现提高了对沿海上升流系统中小型真核浮游生物群落的理解,突出了这些环境中新多样性的巨大潜力。
Unveiling Short-Scale Responses: How Pico- and Nanoeukaryotic Plankton Navigate Environmental Variability in a Coastal Upwelling System
For decades, identifying pico- and nanoeukaryotic plankton has been challenging due to their small size, leaving a significant gap in our knowledge of their composition and dynamics in comparison with their larger counterparts. The advent of molecular techniques unlocked new possibilities for exploring this hidden diversity. We applied metabarcoding targeting the V9 region of 18S rDNA to discern the principal taxonomic groups of pico- and nanoeukaryotes in the Ría de Vigo during the upwelling season. Nanoeukaryotes (NE) exhibit greater diversity compared to picoeukaryotes (PE). Specifically, NE were mainly comprised of nano-sized diatoms and dinoflagellates, many of them uncategorized novel species. Within PE, Syndiniales and Marine Stramenopiles (MAST) were the main components identified. We also captured short-term changes in the biomass and composition of PE an NE, with advection emerging as one of the most significant drivers. Most notably was the ocean inflow of unassigned picoeukaryotes into the Ría, likely driven by the negative circulation during downwelling. Moreover, local grazing within the Ría seems to be important enough to alter NE dynamics, but has a minimal effect over PE. Our findings improve the understanding of the small eukaryotic plankton community in coastal upwelling systems, highlighting a significant potential for novel diversity within these environments.
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.