Trace metals in deep ocean waters: A review

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Corrigendum: Resolving the abundance and air-sea fluxes of airborne microorganisms in the North Atlantic Ocean

A corrigendum on Resolving the abundance and air-sea fluxes of airborne microorganisms in the North Atlantic Ocean by Mayol, E., Jiménez, M. A., Herndl, G. J., Duarte, C. M., and Arrieta, J. M. (2014). Front. Microbiol. 5:557. doi: 10.3389/fmicb.2014.00557 We found an implementation error in the calculation of the deposition velocity (vd) which, in turn, affected all the estimated vd-depending parameters (deposition flux, residence time, and traveled distance by microorganisms). Deposition fluxes are now somewhat lower than previously estimated, resulting in residence times and traveled distances longer than those previously estimated. In addition, the spray fluxes were calculated using a spray generation function (dF/dr0) valid for droplets of radii between 0.5 and 12 μm proposed by Blanchard (1963) and Gathman (1982) as corrected by Andreas et al. (1995). However, in the calculation of dF/dr0, we exceeded this valid range of radii given that we included droplets with radii from 0.2 μm according to the small size of some microbial cells. Thus, a different formulation of dF/dr0, developed by Gong (2003), is now used for the estimation of spray fluxes of microbes, which is valid even for small droplets from a radius of 0.07 μm. Below, we offer a new corrected version of the paragraphs affected by corrections along the text. In addition, we show corrected versions of Figure 1 (forward trajectories according residence times), Figure 3 (deposition velocity values), Figure 5 (spray and deposition fluxes), Figure 6 (Net fluxes), and Table 1. The authors apologize for the errors in the estimates reported in the original manuscript. These corrections only affect the magnitude of some of the reported variables and even though they do not change the scientific conclusions of the article they are reported here for accuracy and reproducibility

Boat anchoring impacts coastal populations of the pen shell, the largest bivalve in the Mediterranean

The decline of important coastal habitats, like seagrass meadows, is likely to influence populations of associated species, like the noble pen shell, Pinna nobilis. Here we used a Bayesian formulation of individual covariate models to derive a reliable estimate of populations of P. nobilis in shallow, and thus usually most impacted, areas around the island of Majorca, Balearic Islands, Spain. At six evaluated sites we find quite distinct densities ranging from 1.4 to 10.0 individuals/100 m2. These differences in density could not be explained by habitat factors like shoot density and meadow cover, nor did dislodgement by storms (evaluated by maximum wind speeds at the sites) seem to play an important role. However, noble pen shell density was related to anchoring as at sites where anchoring was not permitted the average density was 7.9 individuals/100 m2 while in sites where ships anchored the density was on average 1.7 individuals/100 m2. As for the conservation of Posidonia oceanica meadows, for the associated population of P. nobilis it would be of utmost importance to reduce anchoring pressure as a conservation measure for these endangered and protected bivalvesVersión del editor

Recent trends reversal for declimimg European seagrass meadows

Seagrass meadows, key ecosystems supporting fisheries, carbon sequestration and coastal protection, are globally threatened. In Europe, loss and recovery of seagrasses are reported, but the changes in extent and density at the continental scale remain unclear. Here we collate assessments of changes from 1869 to 2016 and show that 1/3 of European seagrass area was lost due to disease, deteriorated water quality, and coastal development, with losses peaking in the 1970s and 1980s. Since then, loss rates slowed down for most of the species and fastgrowing species recovered in some locations, making the net rate of change in seagrass area experience a reversal in the 2000s, while density metrics improved or remained stable in most sites. Our results demonstrate that decline is not the generalised state among seagrasses nowadays in Europe, in contrast with global assessments, and that deceleration and reversal of declining trends is possible, expectingly bringing back the services they provide

Airborne Prokaryote and Virus Abundance Over the Red Sea

Aeolian dust exerts a considerable influence on atmospheric and oceanic conditions negatively impacting human health, particularly in arid and semi-arid regions like Saudi Arabia. Aeolian dust is often characterized by its mineral and chemical composition; however, there is a microbiological component of natural aerosols that has received comparatively little attention. Moreover, the amount of materials suspended in the atmosphere is highly variable from day to day. Thus, understanding the variability of atmospheric dust loads and suspended microbes throughout the year is essential to clarify the possible effects of dust on the Red Sea ecosystem. Here, we present the first estimates of dust and microbial loads at a coastal site on the Red Sea over a 2-year period, supplemented with measurements from dust samples collected along the Red Sea basin in offshore waters. Weekly average dust loads from a coastal site on the Red Sea ranged from 4.6 to 646.11 μg m−3, while the abundance of airborne prokaryotic cells and viral-like particles (VLPs) ranged from 77,967 to 1,203,792 cells m−3 and from 69,615 to 3,104,758 particles m−3, respectively. To the best of our knowledge, these are the first estimates of airborne microbial abundance in this region. The elevated concentrations of resuspended dust particles and suspended microbes found in the air indicate that airborne microbes may potentially have a large impact on human health and on the Red Sea ecosystem

Bathypelagic fauna as a main driver of carbon sequestration in the ocean

Sequestration, in contrast to export, is a mechanism of the biological pump occurring when carbon cannot return to the atmosphere in at least 100 years, normally the carbon transported below 1000 m depth. Pelagic fauna release carbon at depth through respiration, egestion, excretion, moulting, lipid consumption and mortality supporting deep-sea food webs. Knowledge about this transport in the mesopelagic layer is growing. However, the role of the pelagic fauna to fuel the bathypelagic zone, the layer where effective carbon sequestration occurs, is largely unknown. Here we report net zooplankton biomass in the meso- and bathypelagic zones showing significant relationships with primary production (PP) at a global scale during the Malaspina Circumnavigation Expedition. We also reviewed available data on zooplankton biomass at the different biogeographical provinces also showing significant correlations with large-scale estimates of PP, implying the transference of a significant fraction of PP from the epipelagic to the deep ocean. Carbon sequestration assessed only from conservative estimates of zooplankton mortality in the bathypelagic was 0.43 PgC y-1, in the order of recent estimates of gravitational carbon sequestration. These values and those recently reviewed due to lipid consumption almost triples ocean carbon sequestration estimates in Westerlies and Polar biomes. These results point at a pivotal role of the pelagic fauna in ocean carbon sequestration as, besides zooplankton, downward transport by macroplankton and micronekton should also be accounted for. Our results raises the question of whether we are severely underestimating carbon sequestration in the ocea

Large-scale ocean connectivity and planktonic body size

Global patterns of planktonic diversity are mainly determined by the dispersal of propagules with ocean currents. However, the role that abundance and body size play in determining spatial patterns of diversity remains unclear. Here we analyse spatial community structure - β-diversity - for several planktonic and nektonic organisms from prokaryotes to small mesopelagic fishes collected during the Malaspina 2010 Expedition. β-diversity was compared to surface ocean transit times derived from a global circulation model, revealing a significant negative relationship that is stronger than environmental differences. Estimated dispersal scales for different groups show a negative correlation with body size, where less abundant large-bodied communities have significantly shorter dispersal scales and larger species spatial turnover rates than more abundant small-bodied plankton. Our results confirm that the dispersal scale of planktonic and micro-nektonic organisms is determined by local abundance, which scales with body size, ultimately setting global spatial patterns of diversit