Archive for phosphorus

Role for iron in controlling microbial phosphorus acquisition in the ocean

Posted by mmaheigan 
· Thursday, October 12th, 2017 

In the subtropical North Atlantic, dissolved inorganic phosphorus (DIP) concentrations are depleted and might co-limit N2 fixation and microbial productivity. There are relatively large pools of dissolved organic phosphorus (DOP), but microbes need an enzyme to access this P source. One such alkaline phosphatase (APase) enzyme requires zinc (Zn) as its activating cofactor. This has been known for almost 30 years. However, recent crystallography studies revealed that two other widespread APase enzymes contain Fe. Via this requirement, Fe availability could regulate microbial access to the DOP pool.

As detailed in a recent publication in Nature Communications (Browning et al. 2017), this hypothesis was tested on a cruise across the tropical North Atlantic by adding Fe and Zn to incubated seawater and monitoring changes in bulk APase using a simple fluorescence assay. Adding Fe significantly increased APase activity in seawater samples collected in areas that were far-removed from coastal and aerosol Fe sources. Despite seawater Zn concentrations being much lower than Fe, it appeared not to be limiting.

 

Iron (Fe) and zinc (Zn) enrichment experiments conducted in the DIP-depleted tropical North Atlantic suggested that Fe, not Zn, could limit alkaline phosphatase activity (APA). DIP*=DIP–DIN/16, and represents excess DIP availability assuming a 16-fold higher microbial N requirement. Results in the bar chart represent a subset of treatments from one experiment (out of eight conducted).

DIP is depleted in surface waters of the tropical North Atlantic because inputs of North African aerosol Fe stimulates N2 fixation and leads to microbial drawdown of DIP. If the modern ocean is a good analog for the past, the lack of APase stimulation following experimental Zn addition could reflect limited evolutionary selection for Zn-containing APase. In general, DIP is only substantially depleted where there is enhanced Fe input fueling N2 fixation; it therefore follows that any significant requirement for APases might be restricted to these relatively high-Fe, low-Zn waters.

On a shorter timescale, growing anthropogenic nitrogen input to the ocean relative to phosphorus could result in more prevalent oceanic phosphorus deficiency. Corresponding iron inputs might then serve as an important control on phosphorus availability for microbes in these regions.

 

Authors:

Tom Browning (GEOMAR Helmholtz Centre for Ocean Research, Kiel, Germany)
Eric Achterberg (GEOMAR) 
Jaw Chuen Yong (GEOMAR)
Insa Rapp (GEOMAR)
Caroline Utermann (GEOMAR) 
Anja Engel (GEOMAR)
Mark Moore (Ocean and Earth Science, University of Southampton, Southampton, UK)

 

Sinking particles as biogeochemical hubs for trace metal cycling and release

Posted by mmaheigan 
· Thursday, September 14th, 2017 

The extent to which the return of major and minor elements to the dissolved phase in the deep ocean (termed remineralization) is decoupled plays a major role in setting patterns of nutrient limitation in the global ocean. It is well established that major elements such as phosphorus, silicon, and carbon are released at different rates from sinking particles, with major implications for nutrient recycling. Is this also the case for trace metals?

A recent publication by Boyd et al. in Nature Geoscience provides new insights into the biotic and abiotic processes that drive remineralization of metals in the ocean.  Particle composition changes rapidly with depth with both physical (disaggregation) and biogeochemical (grazing; desorption) processes leading to a marked decrease in the total surface area of the particle population. The proportion of lithogenic metals in sinking particles also appears to increase with depth, as the biogenic metals may be more labile and hence more readily removed.

Findings from GEOTRACES process studies revealed that release rates for trace elements such as iron, nickel, and zinc vary from each other. Microbes play a key role in determining the turnover rates for nutrients and trace elements. Decoupling of trace metal recycling in the surface ocean and below may result from their preferential removal by microbes to satisfy their nutritional requirements. In addition, the chemistry operating on particle surfaces plays a pivotal role in determining the specific fates of each trace metal. Teasing apart these factors will take time, as there is a complex interplay between chemical and biological processes. Improving our understanding is crucial, as these processes are not currently well represented by state-of-the-art ocean biogeochemical models.

Figure caption: Rapid changes in the characteristics of sinking particles over the upper 200 m as evidenced by: a) differential release of trace metals from sinking diatoms; b) changes in proportion of lithogenic versus biogenic materials; and c) ten-fold decrease in total particle surface area.

 

Authors:
Philip Boyd (IMAS, Australia)
Michael Ellwood (ANU, Australia)
Alessandro Tagliabue (Liverpool, UK)
Ben Twining (Bigelow, USA)

 

Relevant links:
GEOTRACES Digest: Iron Superstar

Joint workshop with GEOTRACES in August 2016: Biogeochemical Cycling of Trace Elements within the Ocean

Do rivers supply nutrients to the open ocean?

Posted by mmaheigan 
· Wednesday, May 24th, 2017 

Rivers carry large amounts of nutrients (e.g., nitrogen and phosphorus) to the sea, but we do not know how much of that riverine nutrient supply escapes biological and chemical processing in shallow coastal waters to reach the open ocean. Most global ocean biogeochemical models, which are typically unable to resolve coastal processes, assume that either all or none of the riverine nutrients entering coastal waters actually contribute to open ocean processes.

While we know a good deal about the dynamics of individual rivers entering the coastal ocean, studies to date have been limited to a few major river systems, mainly in in developed countries. Globally, there are over 6,000 rivers entering the coastal ocean. In a recent study, Sharples et al (2017) devised a simple approach to obtain a global-scale estimate of riverine nutrient inputs based on the knowledge that low-salinity waters entering the coastal ocean tend to form buoyant plumes that turn under the influence of Earth’s daily rotation to flow along the coastline. Using published data on such flows and incorporating the effect of Earth’s rotation, they obtained estimates of typical cross-shore plume width and compared them to the local width of the continental shelf. This was used to calculate the residence time of riverine nutrients on the shelf, which is the key to estimating how much of a given nutrient is consumed in shelf waters vs. how much is exported to the open ocean.

Global distribution of the amount of riverine dissolved inorganic nitrogen that escapes the continental shelf to reach the open ocean.

The results indicate that, on a global scale, 75% (80%) of the nitrogen (phosphorus) supplied by rivers reaches the open ocean, whereas 25% (20%) of the nitrogen (phosphorus) is consumed on the shelf (e.g., fueling coastal productivity). Limited knowledge of nutrient cycling and consumption in shelf waters represents the primary source of uncertainty in this study. However, well-defined global patterns related to human land use (e.g., agricultural fertilizer use in developed nations) emerged from this analysis, underscoring the need to understand how land-use changes and other human activities will alter nutrient delivery to the coastal ocean in the future.

 

Authors:
Jonathan Sharples (School of Environmental Sciences, University of Liverpool, UK)
Jack Middelburg (Department of Earth Sciences, Utrecht University, Netherlands)
Katja Fennel (Department of Oceanography, Dalhousie University, Canada)
Tim Jickells (School of Environmental Sciences, University of East Anglia, UK)

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