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Archive for New OCB Research – Page 19

Impacts of atmospheric nitrogen deposition and coastal nitrogen fluxes on oxygen concentrations in Chesapeake Bay

Posted by mmaheigan

· Tuesday, April 30th, 2019

How do atmospheric and oceanic nutrients impact oxygen concentrations in the Chesapeake Bay? Generally, researchers focus on how terrestrial nutrients impact hypoxia. The relative importance of river, atmosphere, and ocean inputs have not been quantified, largely because estimates of nitrogen fluxes from the atmosphere and ocean are limited.

A recent study in Journal of Geophysical Research: Oceans quantified the relative impacts of atmospheric and oceanic nitrogen inputs on dissolved oxygen (DO) in the Chesapeake Bay. The authors combined a 3-D biogeochemical model and estimates of atmospheric deposition from the Community Multiscale Air Quality model and interpolations of nitrogen concentrations along the continental shelf from the Ocean Acidification Data Stewardship Project. Atmospheric nitrogen deposition and coastal nitrogen fluxes most impact Chesapeake Bay DO concentrations during the summer when surface waters are depleted in nitrogen. Overall, atmospheric nitrogen deposition has about the same gram-for-gram impact on Chesapeake Bay DO as riverine loading. Although all three nutrient sources vary spatially and temporally, in the central bay, where summer hypoxia is most prevalent, coastal nitrogen fluxes and atmospheric nitrogen fluxes have roughly the same impact on bottom oxygen as a ~10% change in riverine nitrogen loading (Figure 1).

Figure caption: (Left) Four-year (2002–2005) average increase in DO in the summer by removing the atmospheric nitrogen deposition (AtmN), reducing the riverine loading (ΔRiverN) by ~10% (roughly equivalent to turning off the atmospheric deposition), and removing the nitrogen fluxes from the continental shelf (CoastalN). (Right) Relative impacts of the three nitrogen modification scenarios on summertime bottom DO.

These results indicate that two often-neglected sources of nitrogen—direct atmospheric deposition and fluxes of nitrogen from the continental shelf—substantially impact Chesapeake Bay DO, especially in the summer. Future study is needed to investigate the long-term trend of these relative impacts by continued coordination between modeling and observational work, such as applying higher-resolution atmospheric deposition products and integrating more in situ data along the model ocean boundary when they are available. These efforts will improve our understanding of the impacts of different nutrient sources on biogeochemical cycles in coastal water bodies.

Authors:
Fei Da (VIMS, College of William & Mary)
Marjorie A. M. Friedrichs (VIMS, College of William & Mary)
Pierre St-Laurent (VIMS, College of William & Mary)

Northeast Pacific time-series reveals episodic events as major player in carbon export

Posted by mmaheigan

· Tuesday, April 16th, 2019

Temporal fluctuations in the oceanic carbon budget play an important role in the cycling of organic matter from production in surface waters to consumption and sequestration in the deep ocean. A 29-year time-series (1989-2017) of particulate organic carbon (POC) fluxes and seafloor measurements of oxygen consumption in the abyssal northeast Pacific (Sta. M, 4,000 m depth) recently revealed an increasing proportional contribution from episodic events over the past seven years. From 2011 to 2017, 43% of POC flux arrived during high-magnitude (≥ mean + 2 σ) episodic events. Time lags between changes in satellite-estimated export flux (EF), POC flux to the seafloor, and seafloor oxygen consumption varied from 0 to 70 days among six flux events, which could be attributed to variable remineralization rates and/or particle sinking speeds. The Martin equation, a commonly used model to estimate carbon flux, predicted background fluxes well but missed episodic fluxes, subsequently underestimating the measured fluxes by almost 50% (Figure 1). This study reveals the potential importance of episodic POC pulses into the deep sea in the oceanic carbon budget, which has implications for observing infrastructure, model development, and field campaigns focused on quantifying carbon export.

Figure Caption: (A) Station M POC flux measured from sediment traps compared to Martin model estimates, from 1989 to 2017. (B) Model performance for years with >50% sampling coverage: (POC flux_Martin − POC flux_trap)/POC flux_trap 100.

Authors:
Kenneth Smith (MBARI)
Henry Ruhl (MBARI, NOC)
Christine Huffard (MBARI)
Monique Messié (MBARI, Aix Marseille Université)
Mati Kahru (Scripps)

Ocean color offers early warning signal of climate change’s impact on marine phytoplankton

Posted by mmaheigan

· Monday, April 15th, 2019

Marine phytoplankton form the foundation of the marine food web and play a crucial role in the earth’s carbon cycle. Typically, satellite-derived Chlorophyll a (Chl a) is used to evaluate trends in phytoplankton. However, it may be many decades (or longer) before we see a statistically significant signature of climate change in Chl a due to its inherently large natural variability. In a recent study in Nature Communications, authors explored how other metrics, in particular the color of the ocean, may show earlier and stronger signals of climate change at the base of the marine food web.

Figure 1. Computer model results indicating the year in which the signature of climate change impact is larger than the natural variability for (a) Chl a, and (b) remotely sensed reflectance in the blue-green waveband. White areas indicate where there is not a statistically significant change by 2100, or for regions that are currently ice-covered.

In this study, the authors use a unique marine physical-biogeochemical and ecosystem model that also captures how light penetrates the ocean and is reflected upward. The model shows that over the course of the 21^st century, remote sensing reflectance (R_RS, the ratio of upwelling radiance to the downwelling irradiance at the ocean’s surface) in the blue-green portions of the light spectrum is likely to have an earlier, more spatially extensive climate change-driven signal than Chl a (Figure 1). This is because R_RS integrates not only changes to Chl a, but also alterations in other optically important water constituents. In particular, R_RS also captures changes in phytoplankton community structure, which strongly affects ocean optics and is likely to be altered over the 21^st century. Monitoring the response of marine phytoplankton to climate change is important for predicting changes at higher trophic levels, including commercial fisheries. Our study emphasizes the importance of 1) maintaining ocean color sensor compatibility and long-term stability, particularly in the blue-green wavebands; 2) maintaining long-term in situ time-series of plankton communities – e.g., the Continuous Plankton Recorder survey and repeat stations (e.g., HOT, BATS); and 3) reducing uncertainties in satellite-derived phytoplankton community structure estimates.

Authors:
Stephanie Dutkiewicz, Oliver Jahn (Massachusetts Institute of Technology)
Anna E. Hickman (University of Southampton)
Stephanie Henson (National Oceanography Centre Southampton)
Claudie Beaulieu (University of California, Santa Cruz)
Erwan Monier (University of California, Davis)

Antarctic Ocean CO2 helped end the ice age

Posted by mmaheigan

· Tuesday, April 2nd, 2019

Many scientists have long hypothesized that the ocean around Antarctica was responsible for changing CO₂ levels during ice ages, but lacked definitive evidence. A new study in Nature provides the most direct evidence of this process to date and provides crucial evidence of the mechanisms—including changing sea ice cover and bipolar seesaw (warming in the Southern Hemisphere during cooling in the Northern Hemisphere) events—that controlled CO₂ and climate during the ice ages.

Using samples of fossil deep-sea corals collected from 1000 m in the Drake Passage (Figure 1a), the authors were able to reconstruct the CO₂ content of the deep ocean. They found that the deep ocean CO₂ record was the “mirror image” of CO₂ in the atmosphere (Figure 1b), with the ocean storing CO₂ during an ice age and releasing it back to the atmosphere during deglaciation. CO₂ rise during the last ice age occurred in a series of steps and jumps associated with intervals of rapid climate change.

As well as helping scientists better understand the ice ages, the new findings also provide context to current CO₂ rise and climate change. Although the CO₂ rise that helped end the last ice age was dramatic in geological terms, CO₂ rise due to human activity over the last 100 years is even larger and about 100 times faster. CO₂ rise at the end of the ice age helped drive major melting of ice sheets resulting in sea level rise of >100 meters. These results bolster the idea that if we want to prevent dangerous levels of global warming and sea level rise in the future, we need to reduce CO₂ emissions as quickly as possible

Authors:
J. W. B. Rae (University of St Andrews, UK)
A. Burke (University of St Andrews, UK)
L. F. Robinson (University of Bristol, UK)
J. F. Adkins (California Institute of Technology)
T. Chen (University of Bristol, UK, Nanjing University, China)
C. Cole (University of St Andrews, UK)
R. Greenop (University of St Andrews, UK)
T. Li (University of Bristol, UK, Nanjing University, China)
E. F. M. Littley (University of St Andrews, UK)
D. C. Nita (University of St Andrews, UK, Babes-Bolyai University, Romania)
J. A. Stewart (University of St Andrews, UK, University of Bristol, UK)
B. J. Taylor (University of St Andrews, UK)

A half century perspective: Seasonal productivity and particulates in the Ross Sea

Posted by mmaheigan

· Tuesday, April 2nd, 2019

Studies of cruise observations in the Ross Sea are typically biased to a single or a few year(s), and long-term trends have predominantly come from satellites. Consequently, the in situ climatological patterns of nutrients and particulate matter have remained vague and unclear. What are the typical patterns of nutrients and particulate matter concentrations in the Ross Sea in spring and summer? How do these concentrations affect annual productivity estimates?

Patterns of nutrient and particulate matter in the Ross Sea can play a wide-ranging role in a productive region like the Ross Sea. Smith and Kaufman (2018) recently synthesized austral spring and summer (November to February) observations from 42 Ross Sea research cruises (1967-2016) to analyze broad biogeochemical patterns. The resulting climatologies revealed interesting seasonal patterns of nutrient uptake and particulate organic carbon (POC) to chlorophyll (chl) ratios (POC:chl). Temporal patterns in the nitrate and phosphate climatologies confirm the role of early spring haptophyte (Phaeocystis antarctica) growth, followed by limited nitrogen and phosphorus removal in summer. However, a notable increase in POC occurred later in summer that was largely independent of chlorophyll changes, resulting in a dramatic increase in POC:chl. A gradual decline in silicic acid concentrations throughout the summer, along with an increased occurrence of biogenic silica during this time suggest that diatoms may be responsible for this later POC spike. Revised estimates of primary productivity based on these observed climatological POC:chl ratios suggests that summer blooms may be a significant contributor to seasonal productivity, and that estimates of productivity based on satellite pigments underestimate annual production by at least 70% (Figure 1).

Figure 1. Bio-optical estimates of mean productivity using a constant POC:chl ratio (black dots and lines) and modified estimates of productivity using the monthly climatological POC:chl ratios (red dots and lines), in a) the Ross Sea polynya region and b) the western Ross Sea region.

By clarifying typical seasonal patterns of nutrient uptake and POC:chl, these climatologies underscore the biogeochemical importance of both spring haptophyte growth and previously underestimated summer diatom growth in the Ross Sea. Further investigation of the causes and consequences of elevated summer ratios is needed, as assessments of regional food webs and biogeochemical cycles depend on more accurate understanding of primary productivity patterns. Likewise, these results highlight the need for continued efforts to constrain satellite productivity estimates in the Ross Sea using in situ constituent ratios.

For other relevant work on seasonal biogeochemical patterns in the Ross Sea, please see https://doi.org/10.1016/j.dsr2.2003.07.010. And for intra-seasonal estimates of particulate organic carbon to chlorophyll using gliders, please see: https://doi.org/10.1016/j.dsr.2014.06.011.

Authors:
Walker O. Smith Jr. (VIMS, College of William and Mary)
Daniel E. Kaufman (VIMS, College of William and Mary; now at Chesapeake Research Consortium)

Pteropod populations stable or increasing according to long-term study along the Western Antarctic Peninsula

Posted by mmaheigan

· Thursday, March 21st, 2019

Shelled pteropods (pelagic snails) are abundant planktonic predators and prey, linking grazers and higher trophic levels and contributing to the carbon cycle via consumption and excretion. Pteropods have been heralded as bioindicators of ocean acidification, given their aragonitic shell’s susceptibility to dissolution, which could ultimately lead to declining abundance. However, pteropod population dynamics are understudied, particularly in the Southern Ocean, a region predicted to be highly impacted by both warming and ocean acidification. In a recent publication in Limnology and Oceanography, long-term data sets from the Western Antarctic Peninsula show that while there is considerable interannual variability in pteropod abundance, populations have remained stable over the past 25 years, with some pteropod species (gymnosomes (non-shelled pteropod) overall, L. antarctica and C. pyramidata (shelled pteropods) regionally) even increasing during this period (Figure 1).

Figure 1. Annual pteropod abundance anomalies for the entire Palmer Antarctica Long-Term Ecological Research (LTER) study region along the Western Antarctic Peninsula. (a) Limacina helicina antarctica (shelled pteropod), (b) Gymnosomes – nonshelled pteropods that prey on shelled pteropods (p = 0.007, r² = 0.27), and (c) Clio pyramidata (shelled pteropod). Effect of environment on pteropod abundance. (d) SST vs. L. antarctica abundance, e) Sea ice advance vs. L. antarctica and Gymnosome abundance, (f) Sea ice retreat vs. C. pyramidata abundance. Data plotted are annual anomalies for each year of the time series (1993–2017). Sea ice advance is lagged 2-yr behind pteropod abundance (e.g., 2017 pteropod annual anomaly is plotted against 2015 sea ice advance annual anomaly) SST are lagged 1-yr behind L. antarctica abundance (e.g., 2017 L. antarctica annual anomaly is plotted against 2016 SST). Regression lines for significant linear relationships are shown, regression statistics are as follows: (d) SST vs. L. antarctica (circles): n = 25, p = 0.006, r² = 0.25 (e) sea ice advance vs. L. antarctica (filled-circles) and Gymnosomes (empty-circles): n = 25, p = 0.003, r² = 0.30 (dashed line); (f) sea ice retreat vs. C. pyramidata (squares): n = 14, p = 0.0003, r² = 0.64.

There was no significant influence of carbonate chemistry parameters (e.g., aragonite saturation state) on pteropod abundance, since the Western Antarctic Peninsula has yet to experience prolonged conditions characteristic of ocean acidification. However, other environmental factors such as warming and associated sea ice retreat were more influential. For example, warmer, ice-free waters in one year typically led to higher pteropod abundances the following year, suggesting that pteropods may be better adapted than expected to warming conditions due to climate change. The authors propose that earlier sea ice retreat promotes recruitment and subsequent expansion of pteropods further South, which could explain their increased abundance in this subregion. These results increase our understanding of pteropod responses to environmental variability, which is important for predicting future effects of climate change on regional carbon cycling and plankton trophic interactions in the Southern Ocean.

Authors:
Patricia S. Thibodeau (VIMS)
Deborah K. Steinberg (VIMS)
Sharon E. Stammerjohn (University of Colorado at Boulder)
Claudine Hauri (University of Alaska Fairbanks)

Zooplankton vertical migrations represent a significant source of carbon export in the ocean

Posted by mmaheigan

· Friday, March 15th, 2019

Huge numbers of tiny marine animals, known as zooplankton, migrate between the surface ocean and the twilight zone (200 – 1,000 m below the surface) everyday; it is the largest migration event anywhere on the planet. How much carbon do these animals transport with them and how much do they leave behind sequestered in the deep ocean? In a recent publication in Global Biogeochemical Cycles, Archibald et al. (2019) used a simple model to estimate the magnitude of carbon flux into the twilight zone from zooplankton vertical migrations and observed that it was a significant contributor to carbon export on a global scale. The study also revealed strong regional patterns in migration-mediated carbon flux, with the greatest impact on export occurring at subtropical latitudes (Figure 1).

Figure 1. Percent increase in the modeled carbon export flux out of the surface ocean as a result of zooplankton vertical migrations.

Migrating zooplankton also consume significant amounts of oxygen at depth, generating a local maximum in the oxygen utilization profile at depth within the migration layer. By including the effect of the metabolism of migrating zooplankton, the model is able to produce a more detailed picture of oxygen utilization over the twilight zone. The model in this study effectively simulates the complex phenomenon of zooplankton vertical migrations, providing a simple framework that will allow researchers to investigate how this key component of the global carbon cycle might change under future climatic conditions. For example, if increased stratification leads to a greater representation of small cells in phytoplankton communities, then zooplankton migration-mediated carbon export is expected to make up a proportionally larger fraction of the total carbon export flux.

Authors:
Kevin M. Archibald (Woods Hole Oceanographic Institution and Massachusetts Institute of Technology)
David A. Siegel (University of California, Santa Barbara)
Scott C. Doney (University of Virginia)

How fast are elements sinking in the ocean?

Posted by mmaheigan

· Tuesday, March 5th, 2019

The sinking of elements in the ocean influences many important processes such as deep ocean carbon storage and the availability of trace metals for phytoplankton. Previously, quantification of this sinking flux has been done using sediment trap deployments or tracer measurements of a particle-reactive radioisotope. Since sediment traps and each particular radioisotope each have caveats in how they quantify sinking flux, sinking particulate flux measurements, especially trace metal fluxes, are especially sparse, with relatively large uncertainties. For the first time ever, in the U.S. GEOTRACES North Atlantic campaign (GA03), four types of radioisotope data (thorium-234, polonium-210, thorium-228 and thorium-230) were measured, along with a periodic table’s worth of particulate elements that can be used to quantify sinking fluxes at locations with prior sediment trap studies, including the Ocean Flux Program (OFP), for comparison.

Sinking flux estimates of particulate organic carbon (POC) and particulate iron (pFe) derived using different methods, including the different radionuclides labelled and sediment traps from oceanic sites near Bermuda. These include the Bermuda-Atlantic Time-series site (BATS), the Ocean Flux Program site (OFP), and the Bermuda Rise (BaRFlux site). The GA03 and BaRFlux data represent observations from 2012 and 2013. The triangles and stars represent data from throughout the time-series observations of those sites.

In a new study published in Global Biogeochemical Cycles, a team of collaborators synthesized all of the radioisotope and particle composition measurements from the GA03 cruise, as well as results from a nearby study called BaRFlux, to constrain sinking fluxes of carbon and eight trace elements (P, Cd, Co, Cu, Mn, Al, Fe and thorium-232) throughout the North Atlantic Ocean. The five different methods for constraining flux (sediment traps plus the four radioisotope methods) agree encouragingly well given the independent uncertainties associated with each method. Additionally, since the four radioisotopes have a range in half-lives from days to thousands of years, the different methods can reconstruct particle fluxes throughout the water column, from the dynamic bloom-and-bust-like changes near the surface to the relatively slow, long-term sinking into the abyssal ocean. These fluxes will improve the understanding of the global budgets of carbon and trace elements. This study would not have been possible without the support of OCB and GEOTRACES who co-funded a synthesis workshop on biogeochemical cycling of trace elements at the Lamont-Doherty Earth Observatory in summer 2016.

Also see Eos highlight on this article

Authors:
Christopher T. Hayes (University of Southern Mississippi)
Erin E. Black (Woods Hole Oceanographic Institution, now at Dalhousie University)
Robert F. Anderson (Lamont-Doherty Earth Observatory of Columbia University)
Mark Baskaran (Wayne State University)
Ken O. Buesseler (Woods Hole Oceanographic Institution)
Matthew A. Charette (Woods Hole Oceanographic Institution)
Hai Cheng (Xi’an Jiaotong University and University of Minnesota)
Kirk Cochran (Stony Brook University)
Lawrence Edwards (University of Minnesota)
Patrick Fitzgerald (Stony Brook University)
Phoebe J. Lam (University of California Santa Cruz
Yanbin Lu (Earth Observatory of Singapore)
Stephanie O. Morris (Woods Hole Oceanographic institution)
Daniel C. Ohnemus (Bigelow Laboratory for Ocean Sciences, now at Skidaway Institute of Oceanography)
Frank J. Pavia (Lamont-Doherty Earth Observatory of Columbia University)
Gillian Stewart (Queens College, City University of New York)
Yi Tang (Queens College, City University of New York)

You better repeat it: Serial ocean acidification experiments on fish early life stages

Posted by mmaheigan

· Tuesday, March 5th, 2019

To detect potential effects of acidification on marine organisms, experimenters most commonly use within-experiment replication, but repeating the experiments themselves is rarely done. While the first approach suffices to detect major CO₂ effects, other potentially important responses may get detected and robustly quantified only via serial experimentation. A study by Baumann et al. in Biology Letters comprises a meta-analysis of 20 standard CO₂ exposure experiments conducted over six years on Atlantic silverside (Menidia menidia) offspring.

Figure 1: Robust estimate of silverside CO₂ sensitivity based on serial experimentation. (A, B) Mean CO₂ effect size calculated as the log-transformed response ratio of six early life history traits measured at 20 standard experiments between 2012-2017 (Error: bootstrapped 95% confidence intervals). (C) Seasonal change in CO₂ sensitivity in silverside early life stages. Each symbol represents an individual experiment, using offspring obtained by fertilizing wild spawners throughout their spring/summer spawning season.

Silversides are an abundant and ecologically important forage fish in the North Atlantic. The study revealed that during early life stages, Atlantic silversides tolerate pCO₂levels up to ~2,000 µatm, with seasonal shifts in sensitivity. However, this early exposure to high pCO₂ levels reduces embryo survival by 9% and overall survival by 13% (Figure 1). Future ocean acidification could cause reduced survival of these and other forage fish, and thus impact their diverse marine predators, including seabirds and commercially important fish species. This sustained experimental work resulted in the most robustly constrained estimates of average CO₂ effect sizes for a marine organism to date, demonstrating the utility of serial experimentation as a powerful tool for assessing organism responses to changing CO₂.

Authors:
Hannes Baumann
Emma L. Cross
Chris S. Murray
(all University of Connecticut)

Gulf of Mexico: A blue carbon hotspot of mangroves, seagrass and marshes

Posted by mmaheigan

· Wednesday, February 20th, 2019

The Gulf of Mexico (GoM) is an important global hotspot that comprises over 2.1615 million hectares of blue carbon habitats, including mangroves, seagrasses, and salt marshes, which collectively store 480.5 Tg of organic carbon (C_org) just in the upper 1 meter of sediment. Some of these important areas of carbon sequestration are protected or conserved, but much of the area is vulnerable, as 69 million people (US and Mexico) live within 50 miles of these blue carbon habitats, so the potential for development and subsequent habitat loss is high. In a recent study published in Science of the Total Environment, the estuaries around the GoM were delineated to determine areal extent and associated carbon stocks for all three habitats.

Figure 1: Map of blue carbon extent and stock for six sub-regions in the Gulf of Mexico estuaries and the Florida Shelf. The areal extent in hectares (ha) and associated organic carbon (C_org) stock in Tg is listed for each blue carbon system (MN = mangroves, SG = seagrass, SM = saltmarsh) in each sub-region. The underlying blue carbon map shows the distribution of mangroves (red), saltmarsh (yellow), and seagrass (blue) (used with permission from Chmura and Short, 2015).

Of the GoM blue carbon systems studied, mangroves sequester the most carbon, storing nearly 200 Tg C_org over 650,482 ha (Figure 1). Seagrass is ubiquitous throughout the GoM basin, spanning over 1 million ha and storing 184 Tg C_org, Salt marshes, which are predominantly found in the northwestern quadrant of the GoM account for just under 100 Tg C_org. In addition to presenting these updated blue carbon stock estimates for the GoM, this study estimates anthropogenic impacts on GoM blue carbon storage and compares GoM vs. Atlantic shoreline blue carbon habitat stocks and extents.

Authors:
Anitra L. Thorhaug (Yale University)
Helen M. Poulos (Wesleyan University)
Jorge López-Portillo (Instituto de Ecología Mexico)
Jordan Barr (Elder Research)
Ana Laura Lara-Domínguez (Instituto de Ecología Mexico)
Tim C. Ku (Wesleyan University)
Graeme P.Berlyn (Yale University

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.

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