Archive for photosynthesis

How do coccolithophores survive the darkness?

Posted by mmaheigan 
· Friday, April 1st, 2022 

Coccolithophores have survived several major extinction events over geologic time. The most significant was the asteroid impact at the K/T boundary, followed by months of darkness. Additionally, coccolithophores regularly reside in the twilight zone, just beyond the reach of sunlight. A paper recently published in the New Phytologist addresses how these photosynthetic algae can persist and grow, albeit slowly, in darkness using osmotrophy.

The authors discovered that the osmotrophic uptake of certain types of dissolved organic carbon (DOC) can support survival in low light. They completed a 30-day darkness experiment to determine how the concentration of several DOC compounds affects growth. The coccolithophore species Cruciplacolithus neohelis growth rate increased with the increasing concentration of dissolved organic compounds. They also examined the kinetics of short-term uptake of radiolabeled DOC compounds and found that the uptake rate generally showed Michaelis-Menten-like saturation kinetics. All radiolabeled DOC compounds were incorporated into the POC fraction, but surprisingly also into the particulate inorganic carbon (PIC) fraction (i.e., calcite coccoliths).

These results suggest that osmotrophic uptake in coccolithophores may be significant enough to be included in carbon cycle models, especially if they can simultaneously take up a wide range of organic compounds. Surprisingly, we detected 14C-DOC in the PIC fraction after only 24 hours. This remarkably rapid incorporation is most likely due to the respiration of radiolabeled DOC into dissolved inorganic carbon (DIC), subsequently used by coccolithophores for calcification. These results have implications for the biological carbon pump and alkalinity pump paradigms, as we confirmed that both POC and PIC originate from DOC on short time scales.

 

Exploiting phytoplankton as a biosensor for nutrient limitation

Posted by mmaheigan 
· Wednesday, September 15th, 2021 

In the surface ocean, phytoplankton growth is often limited by a scarcity of key nutrients such as nitrogen, phosphorus, and iron. While this is important, there are methodological and conceptual difficulties in characterizing these nutrient limitations.

A recent paper published in Science Magazine leveraged a global metagenomic dataset from Bio-GO-SHIP to address these challenges. The authors characterized the abundance of genes that confer adaptations to nutrient limitation within the picocyanobacteria Prochlorococcus. Using the relative abundance of these genes as an indicator of nutrient limitation allowed the authors to capture expected regions of nutrient limitation, and novel regions that had not previously been studied. This gene-derived indicator of nutrient limitation matched previous methods of assessing nutrient limitation, such as bottle incubation experiments.

These findings have important implications for the global ocean. Characterizing the impact of nutrient limitation on primary production is especially critical in light of future stratification driven by climate change. In addition, this novel methodological approach allows scientists to use microbial communities as an eco-genomic biosensor of adaptation to changing nutrient regimes. For instance, future studies of coastal microbes or other ecosystems may help communities and environmental managers better understand how local microbial populations are adapting to climate change.

 

Watch an illustrated video overview of this research

Authors:
Lucas J. Ustick, Alyse A. Larkin, Catherine A. Garcia, Nathan S. Garcia, Melissa L. Brock, Jenna A. Lee, Nicola A. Wiseman, J. Keith Moore, Adam C. Martiny
(all University of California, Irvine)

Warming counteracts acidification in temperate crustose coralline algae communities

Posted by mmaheigan 
· Friday, November 6th, 2020 

Seawater carbonate chemistry has been altered by dramatic increases in anthropogenic CO2 release and global temperatures, leading to significant changes in rocky shore habitats and the metabolism of most marine organisms. There has been recent interest in how these anthropogenic stresses affect crustose coralline algae (CCA) communities because CCA photosynthesis and calcification are directly influenced by seawater carbonate chemistry. CCA is a foundation species in temperate macroalgal communities, where species succession and rocky shore community structure are particularly susceptible to anthropogenic disturbance. In particular, the disappearance of turf and foliose macroalgae caused by climate change and herbivore pressure results in the dominance of CCA (Figure 1a).

Figure 1: (a) Examples of crustose coralline algae (CCA)-dominated seaweed bed in the East Sea of Korea showing barren ground dominated by CCA (bright white and pink color on the rock; see arrows) on a rocky subtidal zone grazed by sea urchins. (b) Specific growth rate of marginal encrusting area under future climate conditions.

In a recent study published in Marine Pollution Bulletin, the authors conducted a mesocosm experiment to investigate the sensitivity of temperate CCA Chamberlainium sp. to future climate stressors, as simulated by three experimental treatments: 1) Acidification: doubled CO2; 2) Warming: +5ºC; and 3) Greenhouse: doubled CO2 and +5ºC. After a 47-day acclimation period, when compared with present-day (control: 490 μatm and 20ºC) conditions, the Acidification treatment showed decreased photosynthesis rates of Chamberlainium sp, whereas the Warming treatment showed increased photosynthesis. The Acidification treatment also showed reduced encrusting growth rates relative to the Control, but when acidification was combined with warming in the Greenhouse treatment, encrusting growth rates increased substantially (Figure 1b). Taken together, these results suggest that the negative ecophysiological responses of Chamberlainium sp to acidification are ameliorated by elevated temperatures in a greenhouse world. In other words, if the foliose macroalgal community responses negatively in the greenhouse environment, the dominance of CCA will increase further, and the biodiversity of the algae community will be reduced.

 

Authors:
Ju-Hyoung Kim (Faculty of Marine Applied Biosciences, Kunsan National University)
Il-Nam Kim (Department of Marine Science, Incheon National University)

Physics vs. biology in Southern Ocean nutrient gradients

Posted by mmaheigan 
· Tuesday, June 16th, 2020 

In the Southern Ocean, surface water silicate (SiO4) concentrations decline very quickly relative to nitrate concentrations along a northward gradient toward mode water formation regions on the northern edge (Figure 1a, b). These mode waters play a critical role in driving global nutrient concentrations, setting the biogeochemistry of low- and mid-latitude regions around the globe after they upwell further north. To explain this latitudinal surface gradient, most hypotheses have implicated diatoms, which take up and export silicon as well as nitrogen: (1) Diatoms, including highly-silicified species such as Fragilariopsis kerguelensis, are more abundant in the Southern Ocean than elsewhere; (2) Iron limitation, which is prevalent in the Southern Ocean, elevates the Si:N ratio of diatoms; (3) Mass export of empty diatom frustules pumps silicate but not nitrate to deeper waters.

Figure 1: (a) and (b) nitrate and silicate concentrations in surface waters of the Southern Ocean (GLODAPv2_2019 data). (c) Model results of a standard run (black diamonds), a run without biology (red diamonds) and a run without mixing (blue diamonds).

In a recent paper published in Biogeosciences, the authors use an idealized model to explore the relative roles of biological vs. physical processes in driving the observed latitudinal surface nutrient gradients. Over timescales of a few years, removing the effects of biology (no SiO4 uptake or export) from the model elevates silicate concentrations slightly over the entire latitudinal range, but does not remove the strong latitudinal gradient (Figure 1c). However, if the effects of vertical mixing processes such as upwelling and entrainment are removed from the model by eliminating the observed deep [SiO4] gradient, the observed surface nutrient gradient is greatly altered (Figure 1c). These model results suggest that, over short timescales, physics is more important than biology in driving the observed surface water gradient in SiO4:NO3 ratios and forcing silicate depletion of mode waters leaving the Southern Ocean. These findings add to our understanding of Southern Ocean dynamics and the downstream effects on other oceans.

 

Authors:
P. Demuynck (University of Southampton)
T. Tyrrell (University of Southampton)
A.C. Naveira Garabato (University of Southampton)
C.M. Moore (University of Southampton)
A.P. Martin (National Oceanography Centre)

Untangling microbial evolution in the oceans: How the interaction of biological and physical timescales determine marine microbial evolutionary strategies

Posted by mmaheigan 
· Wednesday, March 11th, 2020 

Marine microbes are the engines of global biogeochemical cycling in the oceans. They are responsible for approximately half of all photosynthesis on the planet and drive the ‘biological pump’, which transfers organic carbon from the surface to the deep ocean. As such, it is important to determine how marine microbes will adapt and evolve in response to a changing climate in order to understand and predict how the global carbon cycle may change. However, we still lack a mechanistic understanding of how and how fast microorganisms adapt to stressful and changing environments. This is particularly challenging due to the diversity of organisms that live in the ocean and the dynamic nature of the oceans themselves—microbes are at the whim of ocean currents and so get transported large distances fairly quickly. For the first time, a new study published in PNAS provides a prediction on the controls of microbial evolutionary timescales in the oceans.  The authors hypothesize that there is a trade-off for marine microbes between ability to evolve to long-term changes versus respond to shorter term variability. Their results suggest that marine microbes commonly experience conditions that favor a short-term strategy at the cost of long-term adaptation. This trade-off determines evolutionary timescales and provides a foundation for understanding distributions of microbial traits and biogeochemistry.

Illustration of trade-off in evolutionary strategy as a function of environmental variability. Trajectories where individuals perceived high environmental variability (a & b) exhibited low selective pressure for any one environment but allowed for high environmental tracking. Trajectories where individuals perceived a more stable environment (c&d) had high selective pressure for ’new environments’ (high probability of a selective sweep) but these individuals exhibited poor environmental tracking. Panels a and c show trajectories where selective sweeps were highly probable (red), likely (yellow), and had a low probability (grey). Panels b and d show the estimated persistence of non-genetic modifications necessary for environmental tracking, where grey indicates unrealistically long timescales.

 

Authors:
Nathan G. Walworth (University of Southern California)
Emily J. Zakem (University of Southern California)
John P. Dunne (Geophysical Fluid Dynamics Laboratory, NOAA)
Sinéad Collins (University of Edinburgh)
Naomi M. Levine (University of Southern California)

Tiny marine animals strongly influence the carbon cycle

Posted by mmaheigan 
· Thursday, August 31st, 2017 

What controls the amount of organic carbon entering the deep ocean? In the sunlit layer of the ocean, phytoplankton transform inorganic carbon to organic carbon via a process called photosynthesis. As these particulate forms of organic carbon stick together, they become dense enough to sink out of the sunlit layer, transferring large quantities of organic carbon to the deep ocean and out of contact with the atmosphere.

However, all is not still in the dark ocean. Microbial organisms such as bacteria, and zooplankton consume the sinking, carbon-rich particles and convert the organic carbon back to its original inorganic form. Depending on how deep this occurs, the carbon can be physically mixed back up into the surface layers for exchange with the atmosphere or repeat consumption by phytoplankton. In a recent study published in Biogeosciences, researchers used field data and an ecosystem model in three very different oceanic regions to show that zooplankton are extremely important in determining how much carbon reaches the deep ocean.

Figure 1. Particle export and transfer efficiency to the deep ocean in the Southern Ocean (SO, blue circles), North Atlantic Porcupine Abyssal Plain site (PAP, red squares) and the Equatorial Tropical North Pacific (ETNP, orange triangles) oxygen minimum zone. a) particle export efficiency of fast sinking particles (Fast PEeff) against primary production on a Log10 scale. b) transfer efficiency of particles to the deep ocean expressed as Martin’s b (high b = low efficiency). Error bars in b) are standard error of the mean for observed particles, error too small in model to be seen on this plot.

In the Southern Ocean (SO), zooplankton graze on phytoplankton and produce rapidly sinking fecal pellets, resulting in an inverse relationship between particle export and primary production (Fig. 1a). In the North Atlantic (NA), the efficiency with which particles are transferred to the deep ocean is comparable to that of the Southern Ocean, suggesting similar processes apply; but in both regions, there is a large discrepancy between the field data and the ecosystem model (Fig. 1b), which poorly represents particle processing by zooplankton. Conversely, much better data-model matches are observed in the equatorial Pacific, where lower oxygen concentrations mean fewer zooplankton; this reduces the potential for zooplankton-particle interactions that reduce particle size and density, resulting in a lower transfer efficiency.

This result suggests that mismatches between the data and model in the SO and NA may be due to the lack of zooplankton-particle parameterizations in the model, highlighting the potential importance of zooplankton in regulating carbon export and storage in the deep ocean. Zooplankton parameterizations in ecosystem models must be enhanced by including zooplankton fragmentation of particles as well as consumption. Large field programs such as EXPORTS could help constrain these parameterisation by collecting data on zooplankton-particle interaction rates. This will improve our model estimates of carbon export and our ability to predict future changes in the biological carbon pump. This is especially important in the face of climate-driven changes in zooplankton populations (e.g. oxygen minimum zone (OMZ) expansion) and associated implications for ocean carbon storage and atmospheric carbon dioxide levels.

 

Authors:
Emma L. Cavan (University of Tasmania)
Stephanie A. Henson (National Oceanography Centre, Southampton)
Anna Belcher (University of Southampton)
Richard Sanders (National Oceanography Centre, Southampton)

Scientists reveal major drivers of aragonite saturation state in the Gulf of Maine, a region vulnerable to acidification

Posted by mmaheigan 
· Thursday, May 11th, 2017 

The Gulf of Maine (GoME) is a shelf region that is especially vulnerable to ocean acidification (OA). GoME’s shelf waters display the lowest mean pH, aragonite saturation state (Ω-Ar), and buffering capacity of the entire U.S. East Coast. These conditions are a product of many unique characteristics and processes occurring in the GoME, including relatively low water temperatures that result in higher CO2 solubility; inputs of fresher, low-alkalinity water that is traceable to the rivers discharging into the Labrador Sea to the north, as well as local inputs of low-pH river water; and its semi-enclosed nature (long residence time >1 year), which enables the accumulation of respiratory products, i.e. CO2.

A recent study by Wang et al. (2017) is the first to assess the major oceanic processes controlling seasonal variability of aragonite saturation state and its linkages with pteropod abundance in the GoME. The results indicate that surface production was tightly coupled with remineralization in the benthic nepheloid layer during highly productive seasons, resulting in occasional aragonite undersaturation. Mean water column Ω-Ar and abundance of large thecosomatous pteropods show some correlation, although discrete cohort reproductive success likely also influences their abundance. Photosynthesis-respiration is the primary driving force controlling Ω-Ar variability over the seasonal cycle. However, calcium carbonate (CaCO3) dissolution appears to occur at depth in fall and winter months when bottom water Ω-Ar is generally low but slightly above 1. This is accompanied by a decrease in pteropod abundance that is consistent with previous CaCO3 flux trap measurements.

Figure. Changes of aragonite saturation states (ΔΩ) between three consecutive cruises from April – July 2015 as a function of changes in salinity-normalized DIC (ΔenDIC, including correction of freshwater inputs) (a) and changes in salinity-normalized TA (ΔenTA, including correction of freshwater inputs) (b). The data points circled in (b) represent potential alkalinity sources from CaCO3 dissolution and/or anaerobic respiration. Solid lines are theoretical lines of ΔΩ vs. ΔenDIC and ΔΩ vs. ΔenTA expected if only photosynthesis and respiration/remineralization occur. Dashed lines are theoretical lines if only calcification and dissolution of CaCO3 occur.

Under the current rate of OA, the mean Ω-Ar of the subsurface and bottom waters of the GoME will approach undersaturation (Ω-Ar < 1) in 30-40 years. As photosynthesis and respiration are the major driving mechanisms of Ω-Ar variability in the water column, any biological regime changes may significantly impact carbonate chemistry and the GoME ecosystem, including the CaCO3 shell-building capacity of organisms that are critical to the GoME food web.

 

Author:

Zhaohui Aleck Wang (Woods Hole Oceanographic Institution)

Filter by Keyword

234Th disequilibrium abundance acidification africa air-sea interactions air-sea interface algae alkalinity allometry ammonium AMOC anoxia anoxic Antarctic anthro impacts anthropogenic carbon aquaculture aragonite saturation arctic Argo arsenic artificial seawater Atlantic Atlantic modeling atmospheric carbon atmospheric CO2 atmospheric nitrogen deposition authigenic carbonates autonomous platforms bacteria BATS benthic bgc argo bio-go-ship bio-optical bioavailability biogeochemical cycles biogeochemical cycling biogeochemical models biogeochemistry Biological Essential Ocean Variables biological pump biological uptake biophysics bloom blooms blue carbon bottom water boundary layer buffer capacity C14 CaCO3 calcification calcite carbon-climate feedback carbon-sulfur coupling carbon budget carbon cycle carbon dioxide carbon export carbon sequestration carbon storage Caribbean CCA CCS changi changing marine ecosystems changing marine environments changing ocean chemistry chemical oceanographic data chemical speciation chemoautotroph chesapeake bay chl a chlorophyll circulation climate change climate variability CO2 CO2YS coastal darkening coastal ocean cobalt Coccolithophores community composition conservation cooling effect copepod coral reefs CTD currents cyclone data data access data management data product Data standards DCM dead zone decadal trends decomposers decomposition deep convection deep ocean deep sea coral deoxygenation depth diagenesis diatoms DIC diel migration dimethylsulfide dinoflagellate discrete measurements dissolved inorganic carbon dissolved organic carbon DOC DOM domoic acid dust DVM earth system models ecology ecosystems ecosystem state eddy Education Ekman transport emissions ENSO enzyme equatorial regions error ESM estuarine and coastal carbon estuarine and coastal carbon fluxes estuary euphotic zone eutrophication evolution export export fluxes export production EXPORTS extreme events extreme weather events faecal pellets filter feeders filtration rates fire fish Fish carbon fisheries floats fluid dynamics fluorescence food webs forage fish forams freshening freshwater frontal zone fronts functional role future oceans geochemistry geoengineering geologic time GEOTRACES glaciers gliders global carbon budget global ocean global warming go-ship grazing greenhouse gas Greenland groundwater Gulf of Maine Gulf of Mexico Gulf Stream gyre harmful algal bloom high latitude human food human impact hurricane hydrogen hydrothermal hypoxia ice age ice cores ice cover industrial onset inverse circulation ions iron iron fertilization isotopes jellies katabatic winds kelvin waves krill kuroshio laboratory vs field land-ocean continuum larvaceans lateral transport LGM lidar ligands light light attenuation lipids mangroves marine carbon cycle marine heatwave marine snowfall marshes Mediterranean meltwater mesopelagic mesoscale metagenome metals methane methods microbes microlayer microorganisms microscale microzooplankton midwater mixed layer mixed layers mixotrophy modeling models mode water molecular diffusion MPT multi-decade n2o NAAMES NASA NCP net community production net primary productivity new ocean state new technology Niskin bottle nitrate nitrogen nitrogen fixation nitrous oxide north atlantic north pacific nuclear war nutricline nutrient budget nutrient cycling nutrient limitation nutrients OA ocean-atmosphere ocean acidification ocean acidification data ocean carbon uptake and storage ocean color ocean observatories ocean warming ODZ oligotrophic omics OMZ open ocean optics organic particles oscillation overturning circulation oxygen pacific paleoceanography particle flux pCO2 PDO peat pelagic PETM pH phenology phosphorus photosynthesis physical processes physiology phytoplankton PIC plankton POC polar regions pollutants precipitation predation prediction primary production primary productivity Prochlorococcus proteins pteropods pycnocline radioisotopes remineralization remote sensing repeat hydrography residence time resource management respiration resuspension rivers rocky shore Rossby waves Ross Sea ROV salinity salt marsh satell satellite scale seafloor seagrass sea ice sea level rise seasonal patterns seasonal trends sea spray seaweed sediments sensors shelf system shells ship-based observations shorelines silicate sinking particles size SOCCOM soil carbon southern ocean south pacific spatial covariations speciation SST stoichiometry subduction submesoscale subpolar subtropical sulfate surf surface surface ocean Synechococcus teleconnections temperate temperature temporal covariations thermocline thermodynamics thermohaline thorium tidal time-series time of emergence top predators total alkalinity trace elements trace metals trait-based transfer efficiency transient features Tris trophic transfer tropical turbulence twilight zone upper ocean upper water column upwelling US CLIVAR validation velocity gradient ventilation vertical flux vertical migration vertical transport volcano warming water clarity water quality western boundary currents wetlands winter mixing world ocean compilation zooplankton

Copyright © 2022 - OCB Project Office, Woods Hole Oceanographic Institution, 266 Woods Hole Rd, MS #25, Woods Hole, MA 02543 USA Phone: 508-289-2838  •  Fax: 508-457-2193  •  Email: ocb_news@us-ocb.org

link to nsflink to noaalink to WHOI

Funding for the Ocean Carbon & Biogeochemistry Project Office is provided by the National Science Foundation (NSF) and the National Aeronautics and Space Administration (NASA). The OCB Project Office is housed at the Woods Hole Oceanographic Institution.