The dark ocean is one of the largest biomes on Earth, with critical roles in organic matter remineralization and global carbon sequestration. Despite its recognized importance, little is known about some key microbial players, such as the community of heterotrophic protists (HP), which are likely the main consumers of prokaryotic biomass. To investigate this microbial component at a global scale, we determined their abundance and biomass in deepwater column samples from the Malaspina 2010 circumnavigation using a combination of epifluorescence microscopy and flow cytometry. HP were ubiquitously found at all depths investigated down to 4000 m. HP abundances decreased with depth, from an average of 72 ± 19 cells ml À 1 in mesopelagic waters down to 11 ± 1 cells ml À 1 in bathypelagic waters, whereas their total biomass decreased from 280±46 to 50±14 pg C ml À 1 . The parameters that better explained the variance of HP abundance were depth and prokaryote abundance, and to lesser extent oxygen concentration. The generally good correlation with prokaryotic abundance suggested active grazing of HP on prokaryotes. On a finer scale, the prokaryote:HP abundance ratio varied at a regional scale, and sites with the highest ratios exhibited a larger contribution of fungi molecular signal. Our study is a step forward towards determining the relationship between HP and their environment, unveiling their importance as players in the dark ocean's microbial food web.
Prokaryotic abundance, activity and community composition were studied in the euphotic, intermediate and deep waters off the Galician coast (NW Iberian margin) in relation to the optical characterization of dissolved organic matter (DOM). Microbial (archaeal and bacterial) community structure was vertically stratified. Among the Archaea, Euryarchaeota, especially Thermoplasmata, was dominant in the intermediate waters and decreased with depth, whereas marine Thaumarchaeota, especially Marine Group I, was the most abundant archaeal phylum in the deeper layers. The bacterial community was dominated by Proteobacteria through the whole water column. However, Cyanobacteria and Bacteroidetes occurrence was considerable in the upper layer and SAR202 was dominant in deep waters. Microbial composition and abundance were not shaped by the quantity of dissolved organic carbon, but instead they revealed a strong connection with the DOM quality. Archaeal communities were mainly related to the fluorescence of DOM (which indicates respiration of labile DOM and generation of refractory subproducts), while bacterial communities were mainly linked to the aromaticity/age of the DOM produced along the water column. Taken together, our results indicate that the microbial community composition is associated with the DOM composition of the water masses, suggesting that distinct microbial taxa have the potential to use and/or produce specific DOM compounds.
Analysis of seasonal patterns of marine bacterial community structure along horizontal and vertical spatial scales can help to predict long-term responses to climate change. Several recent studies have shown predictable seasonal reoccurrence of bacterial assemblages. However, only a few have assessed temporal variability over both horizontal and vertical spatial scales. Here, we simultaneously studied the bacterial community structure at two different locations and depths in shelf waters of a coastal upwelling system during an annual cycle. The most noticeable biogeographic patterns observed were seasonality, horizontal homogeneity, and spatial synchrony in bacterial diversity and community structure related with regional upwelling-downwelling dynamics. Water column mixing eventually disrupted bacterial community structure vertical heterogeneity. Our results are consistent with previous temporal studies of marine bacterioplankton in other temperate regions and also suggest a marked influence of regional factors on the bacterial communities inhabiting this coastal upwelling system. Bacterial-mediated carbon fluxes in this productive region appear to be mainly controlled by community structure dynamics in surface waters, and local environmental factors at the base of the euphotic zone.
Even though compelling evidences indicate that marine microbes show biogeographic patterns, very little is known on the mechanisms driving those patterns in aquatic ecosystems. In the present study, bacterial community structure was examined in epipelagic waters of a highly hydrodynamic area of the Southern Ocean to gain insight into the role that biogeochemical factors and water mass mixing (a proxy of dispersal) have on microbial biogeography. Four water masses that converge and mix around the South Shetland Islands (northern tip of the Antarctic Peninsula) were investigated. Bacterioplankton communities were water-mass specific, and were best explained by dispersal rather than by biogeochemical factors, which is attributed to the relatively reduced environmental gradients found in these cold and nutrient rich waters. These results support the notion that currents and water mixing may have a considerable effect in connecting and transforming different water bodies, and consequently, in shaping communities of microorganisms. Considering the multidimensional and dynamic nature of the ocean, analysis of water mass mixing is a more suitable approach to investigate the role of dispersal on the biogeography of planktonic microorganisms rather than geographical distance.
Advancements in chemical, medical, cosmetic, and plastic producing industries have improved agricultural yields, health and human life in general. As a negative consequence, a plethora of chemicals are intentionally and unintentionally released to terrestrial and aquatic environments with sometimes devastating effects for entire ecosystems. One mitigation strategy to counteract this pollution is bioremediation. Bioremediation is an umbrella term for biologically mediated processes during which an undesired compound is transformed, degraded, sequestered and/or entirely removed from the ecosystem. Organisms across all domains of life may mediate bioremediation; yet, fungi are particularly promising candidates. They possess metabolic capabilities to break down complex molecules which make fungi the ultimate degraders of recalcitrant organic matter in nature. Bioremediation by fungi, also termed mycoremediation, has been more frequently investigated in terrestrial than aquatic ecosystems, although fungi also thrive in lacustrine and marine environments. Here, we focus on mycoremediation of emerging pollutants in aquatic environments. In this context, we draw parallels between terrestrial and aquatic fungal taxa, and their role in mycoremediation. We discuss the ability of fungi to break-down (i) pesticides, (ii) pharmaceuticals and personal care products, (iii) plastics, both conventional types and (iv) bioplastics, and fungal role, (v) mitigation of heavy metal pollution. Furthermore, we (vi) discuss possible mycoremediation strategies in applied settings and highlight novel enzyme based mycoremediation strategies.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.