Archive for greenhouse gas

A suite of CO2 removal approaches modeled for the 1.5 ˚C future

Posted by mmaheigan 
· Thursday, August 31st, 2023 

Carbon dioxide removal (CDR) is “unavoidable” in efforts to limit end-of-century warming to below 1.5 °C. This is because some greenhouse gas emissions sources—non-CO2 from agriculture, and CO2 from shipping, aviation, and industrial processes—will be difficult to avoid, requiring CDR to offset their climate impacts. Policymakers are interested in a wide variety of ways to draw down CO2 from the atmosphere, but to date, the modeling scenarios that inform international climate policies have mostly used biomass energy with carbon capture and storage (BECCS) as a proxy for all CDR. It is critical to understand the potential of a full suite of CDR technologies, to understand their interactions with energy-water-land systems and to begin preparing for these impacts.

Figure caption: Each of the six carbon dioxide removal approaches identified in recent U.S. legislation and modeled for this study could bring unique benefits and tradeoffs to the energy-water-land system. This image depicts afforestation, direct ocean capture, direct air capture, biochar, enhanced weathering, and bioenergy with carbon capture and storage in clockwise order. Floating carbon dioxide molecules hover above the landscape (image credit: Nathan Johnson, PNNL).

A recent study published in the journal Nature Climate Change was the first to model six major CDR pathways in an integrated assessment model. The modeled pathways range from bioenergy with carbon storage and afforestation (already represented by most models), also direct air capture, biochar and crushed basalt spreading on global croplands, and electrochemical stripping of CO2 from seawater aka direct ocean capture. The removal potential contributed by each of the six pathways varies widely across different regions of the world. Direct ocean capture showed the smallest removal potential but has important potential synergies with water desalination. This method could help arid regions such as the Middle East meet their water needs in a warming world. Enhanced weathering has much larger (GtCO2-yr-1) removal potential and could potentially help ameliorate ocean acidification. Overall, similar total amounts of CO2 are removed compared to other modeling scenarios, but broader set of technologies lessens the risk that any one of them would become politically or environmentally untenable.

Authors:
Jay Fuhrman  (Joint Global Change Research Institute)
Candelaria Bergero (Joint Global Change Research Institute)
Maridee Weber (Joint Global Change Research Institute)
Seth Monteith (ClimateWorks Foundation)
Frances M. Wang (ClimateWorks Foundation)
Andres F. Clarens (University of Virginia)
Scott C. Doney (University of Virginia)
William Shobe (University of Virginia)
Haewon McJeon (Joint Global Change Research Institute )

Twitter: @pnnlab @climateworks @uva

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)

Arctic rivers as carbon highways

Posted by mmaheigan 
· Tuesday, June 16th, 2020 

Rapid environmental changes in the Arctic will potentially alter the atmospheric emissions of heat-trapping greenhouse gases such as methane (CH4) and carbon dioxide (CO2). A recent study on the Canadian Arctic published in Geophysical Research Letters reveals that spring meltwater delivery drives episodic outgassing events along the lake-river-bay continuum. This spring runoff period is not well-represented in prior studies, which, due to ease of sampling access, have focused more on summertime low-ice conditions. Study authors established a community-based monitoring program in Cambridge Bay and an adjacent inflowing river system in Nunavut, Canada from 2017-2018. These time-series data revealed that at the onset of the melt season river water contains methane concentrations up to 2000 times higher than observed in the bay from late summer through early spring (Figure 1 panel a). In addition, the authors deployed a novel robotic chemical sensing kayak (the ChemYak) in the Bay for five days in 2018 to densely sample water CH4 and CO2 levels in space and time during the spring thaw (Figure 1 panel b). The ChemYak observations revealed that river water containing elevated levels of both of these greenhouse gases flowed into the bay and outgassed to the atmosphere over a period of 5 days! The authors estimate that river inflow during the short melt season drives >95% of all annual methane emissions from the bay. These results demonstrate the need for seasonally-resolved sampling to accurately quantify greenhouse gas emissions from polar systems.

Figure 1: Panel a) Measurements of methane concentration in Cambridge Bay and an adjacent river showed strong seasonality; elevated concentrations were associated with river inflow at the start of the freshet. Panel b) Observations with the ChemYak robotic surface vehicle in Cambridge Bay revealed that excess methane was rapidly ventilated to the atmosphere following ice melt in the bay.

 

Authors
Cara Manning (University of British Columbia)
Victoria Preston (Woods Hole Oceanographic Institution and Massachusetts Institute of Technology)
Samantha Jones (University of Calgary)
Anna Michel (Woods Hole Oceanographic Institution)
David Nicholson (Woods Hole Oceanographic Institution)
Patrick Duke (University of Calgary and University of Victoria)
Mohamed Ahmed (University of Calgary)
Kevin Manganini (Woods Hole Oceanographic Institution)
Brent Else (University of Calgary)
Philippe Tortell (University of British Columbia)

Biological and physical controls on estuarine nitrous oxide emissions

Posted by mmaheigan 
· Tuesday, February 5th, 2019 

Nitrous oxide (N2O) is a potent greenhouse gas with rising atmospheric concentrations. Atmospheric emissions of N2O are predicted to increase with continued anthropogenic perturbation of the nitrogen cycle, yet the magnitude of these emissions is uncertain, particularly in coastal systems where N2O fluxes are poorly constrained. How do N2O emissions from a eutrophic estuary vary in space and time?

Figure 1: Depth profiles of nitrous oxide (N2O) (circles), salinity (dashed line), and dissolved oxygen (solid line) in the Chesapeake Bay at three stations. Solid circles indicate oversaturation of N2O with respect to equilibrium with the atmosphere, and open circles indicate undersaturation.

In a recent publication in Estuaries and Coasts, Laperriere et al. (2018) examined how physical and biological processes influence the distribution of N2O in Chesapeake Bay using dissolved gas measurements (N2O and N2/Ar) and stable isotope tracer incubations. During stratified summer conditions, the mesohaline region of the Chesapeake Bay was always a source of N2O to the atmosphere. The highest N2O concentrations occurred in the pycnocline at the interface between reducing bottom waters and oxygenated surface waters (Figure 1). Vertical mixing of surface waters across the pycnocline caused elevated rates of ammonia oxidation, a biological source of N2O, and resulted in the accumulation of nitrite (NO2–) below the pycnocline. During periods of weak mixing, ammonia oxidation rates and N2O concentrations were lower, and low dissolved oxygen concentrations below the pycnocline set the stage for N2O consumption via denitrification (Figure 1). The interplay between biological and physical processes controlling fluctuations in N2O concentration was examined using a mass balance approach. Mass balance estimates indicated that both biological processes and physical transport contribute to local changes in N2O concentration. The authors suggest that the fate of N2O during stratified summer conditions is governed by vertical mixing across the pycnocline, controlling whether N2O is released to the atmosphere or consumed at depth.

 

Authors:
Sarah M. Laperriere (University of California, Santa Barbara)
Nicholas J. Nidzieko (University of California, Santa Barbara)
Rebecca J. Fox (Washington College)
Alexander W. Fisher (University of California, Santa Barbara)
Alyson E. Santoro (University of California, Santa Barbara)

Evidence against an Arctic Ocean methane bomb

Posted by mmaheigan 
· Tuesday, February 5th, 2019 

Gas hydrates are an ice-like storehouse of the greenhouse gas methane found in continental margins of the world ocean. Warming waters can cause hydrates to decompose and release ancient methane to overlying sediment and waters. The continental shelves of the Arctic Ocean have been thought of as “ground zero” for the potential release of methane from hydrates, since the Arctic is warming rapidly and hydrates are found at relatively shallow water depths there. Another potential ancient methane input to Arctic shelf waters is the methane produced by microorganisms from the gradual thawing of permafrost carbon within seafloor sediment and/or transported to the shelf from terrestrial permafrost via rivers. But, can large stores of ancient-sourced methane reach surface waters and enter the atmosphere, contributing to greenhouse warming?

Figure caption: Map showing the fraction of methane in each surface water sample that was derived from ancient hydrate or permafrost, on a scale from 0 (modern, 0% ancient; indigo) to 1 (100% ancient; yellow). While some of the near-shore surface methane samples have a significant (~50%) ancient component, in waters deeper than 20 m, the surface water methane was mostly (90-95%) derived from modern sources.

To answer this question and understand the role of these ancient sources of methane (hydrates and permafrost), the authors of a 2018 study in Science Advances measured the natural abundance of radiocarbon (14C) in dissolved methane in the shallow shelf waters of the Alaskan Arctic Ocean (U.S. Beaufort Sea); methane derived from ancient sources has little to no measurable 14C because of radioactive decay over time. The 14C-methane results show that ancient sources are contributing methane to the study area’s waters, as the authors predicted. However, ancient methane emitted to seawater can be consumed by microorganisms or transported away by currents before reaching the atmosphere, though these mechanisms have not been known to be effective at removing methane in waters <100 m. This study revealed that these removal processes are surprisingly efficient in shallow shelf waters, especially at the study area’s deepest stations of 30 and 40 m depth, where only ~10% of the methane in surface waters was derived from ancient sources. These results add to a growing body of evidence against the likelihood of a large methane emission to the atmosphere occurring from ancient sources like hydrates, since the authors expect that methane removal processes in the water column are much more efficient in waters 100s of meters deep, where the bulk of the hydrate reservoir resides.

 

Authors:
K.J. Sparrow (University of Rochester; current address: Florida State University)
J.D. Kessler (University of Rochester)
J.R. Southon (University of California Irvine)
Garcia-Tigreros (University of Rochester)
K.M. Schreiner (University of Minnesota Duluth)
C.D. Ruppel (USGS)
J.B. Miller (University of Colorado Boulder; NOAA)
S.J. Lehman (University of Colorado Boulder)
Xu (University of California Irvine)

Arctic surface waters release methane but also absorb 2,000 times the CO2 for a net cooling effect

Posted by mmaheigan 
· Thursday, September 28th, 2017 

A recent study by Pohlman et al. published in PNAS showed that ocean waters near the surface of the Arctic Ocean absorbed 2,000 times more carbon dioxide (CO2) from the atmosphere than the amount of methane released into the atmosphere from the same waters. The study was conducted near Norway’s Svalbard Islands, which overly numerous seafloor methane seeps.

Methane is a more potent greenhouse gas than CO2, but the removal of CO2 from the atmosphere where the study was conducted more than offset the potential warming effect of the observed methane emissions. During the study, scientists continuously measured the concentrations of methane and CO2 in near-surface waters and in the air just above the ocean surface. The measurements were taken over methane seeps fields at water depths ranging from 260 to 8530 feet (80 to 2600 meters).

Figure 1. Ocean waters overlying shallow-water methane seeps (white dots) offshore from the Svalbard Islands absorb substantially more atmospheric carbon dioxide than the methane that they emit to the atmosphere. Colors indicate the strength of the negative greenhouse warming potential associated with carbon dioxide influx to these surface waters relative to the positive greenhouse warming potential associated with the methane emissions. Gray shiptracks have background values for the relative greenhouse warming potential.

Analysis of the data confirmed that methane was entering the atmosphere above the shallowest (water depth of 260-295 feet or 80-90 meters) Svalbard margin seeps. The data also showed that significant amounts of CO2 were being absorbed by the waters near the ocean surface, and that the cooling effect resulting from CO2 uptake is up to 230 times greater than the warming effect expected from the methane emitted.

Most previous studies have focused only on the sea-air flux of methane overlying seafloor seep sites and have not accounted for the drawdown of CO2 that could offset some of the atmospheric warming potential of the methane. Phytoplankton appeared to be more active in the near-surface waters overlying the seafloor methane seeps, which would explain why so much carbon dioxide was being absorbed. Physical and biogeochemical measurements of near-surface waters overlying the seafloor methane seeps showed strong evidence of upwelling of cold, nutrient-rich waters from depth, stimulating phytoplankton activity and increasing CO2 drawdown. This study was the first to document this CO2 drawdown mechanism in a methane source region.

“If what we observed near Svalbard occurs more broadly at similar locations around the world, it could mean that methane seeps have a net cooling effect on climate, not a warming effect as we previously thought,” said USGS biogeochemist John Pohlman, the paper’s lead author. “We are looking forward to testing the hypothesis that shallow-water methane seeps are net greenhouse gas sinks in other locations.”

 

Authors:
John W. Pohlman (USGS Woods Hole Coastal & Marine Science Center)
Jens Greinert (GEOMAR, Univ. of Tromsø, Royal Netherlands Institute for Sea Research)
Carolyn Ruppel (USGS Woods Hole Coastal & Marine Science Center)
Anna Silyakova (Univ. of Tromsø)
Lisa Vielstädte (GEOMAR)
Michael Casso (USGS Woods Hole Coastal & Marine Science Center)
Jürgen Mienert (Univ. of Tromsø)
Stefan Bünz (Univ. of Tromsø)

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