Download PDF
Technical Note  |  Open Access  |  7 Oct 2023

How to quantify blue carbon sequestration rates in seagrass meadow sediment: geochemical method and troubleshooting

Views: 1487 |  Downloads: 269 |  Cited:  1
Carbon Footprints 2023;2:21.
10.20517/cf.2023.37 |  © The Author(s) 2023.
Author Information
Article Notes
Cite This Article

Abstract

Seagrasses take up carbon dioxide and transform it into organic carbon, some of which is buried in meadow sediments. Very high carbon burial rates have been claimed for seagrass meadows globally, and international protocols have been developed with a view to awarding carbon offset credits. However, recent geochemical work has shown that a misunderstanding of how marine sediment buries and processes organic carbon has led to overestimates of at least an order of magnitude. Common blue carbon methodology does not adequately account for bioturbation or remineralization in surface sediment, and there is often a conflation of standing stock with ongoing burial. To determine accurate seagrass carbon burial rates requires the following steps: (1) Determine the sediment accumulation rate below the surface mixed layer, using 210Pb and porosity; (2) Determine the burial concentration of organic carbon; (3) Multiply the sediment accumulation rate by the buried % organic carbon; (4) If excluding allochthonous carbon burial, use biomarkers to determine the proportion of seagrass-derived organic carbon; and (5) Account for the offset due to the burial of carbonate formed inside the meadow. Seagrass meadows provide valuable habitat and protect coastlines from erosion. They can also play a role in short-term carbon sequestration. However, if carbon credits are awarded based on inflated estimates and used to offset emissions elsewhere, the net effect could be an increase in carbon dioxide emissions to the atmosphere.

Keywords

Sediment, blue carbon, seagrass, sequestration, burial, methodology, remineralization, bioturbation

INTRODUCTION

Seagrasses take up carbon dioxide and transform it into organic carbon, burying a portion of it in the meadow sediment. Very high carbon sequestration rates have been claimed for seagrass meadows globally (27-44 TgC yr-1[1], representing 10%-18% of the ocean’s carbon sequestration in just 0.1% of the area[1]). This has led to interest in developing a market for carbon offset credits for their expansion or protection[2]. Because seagrass meadows are undeniably important as critical habitat and for coastline protection, local food security, and ecotourism[3], protecting them seems like a no-regrets activity. However, marine geochemical work has shown that common methodology systematically biases local sequestration rates high, leading to an overestimate of at least an order of magnitude on a global scale[4,5]. If carbon credits are awarded on the basis of overstated sequestration estimates and used to offset increased emissions elsewhere, there could be a net increase in the flux of carbon dioxide to the atmosphere.

Carbon burial in vegetated ecosystems, such as seagrass meadows, cannot truly offset emissions of ancient fossil fuels, because of the orders of magnitude difference in timescale (seasons to hundreds of years for meadow sediment vs. hundreds of millions of years for fossil fuels)[6,7]. However, increased burial in these ecosystems could provide a short-term sink to buy time to consider other options for climate change mitigation.

Standing stock and burial flux give different information about carbon stored in the sediment. Stock is the inventory of organic carbon over a defined depth of sediment, often the top 1 m, e.g.,[8]. It is a measure of the carbon that has already been fixed and stored, and which no longer draws down additional carbon dioxide. Burial flux is a measure of the ongoing rate of capture and burial of carbon.

It is useful to measure stock to quantify and map the vulnerable carbon as a liability assessment of potential future release due to physical disturbance or climate change[9,10], which would add to a country’s total carbon emissions. However, only carbon burial flux represents the potential for ongoing, additional carbon storage. The remainder of this paper will discuss how to calculate carbon burial flux and some important considerations.

Field methods for the collection of sediment cores in seagrass meadows have been described elsewhere, including the importance of site selection[11,12] and reducing and quantifying compaction[13]. The purpose of this Technical Note is to present a specific, step-by-step method for interpreting sediment core profiles in seagrass meadow sediment, building on the author’s previously published, broad critique of common blue carbon methodology[4].

Geochemical oceanographers devised a methodology for determining accurate sedimentation and organic carbon burial rates in marine sediment in the 1970s-1990s, e.g.,[14-18]. This paper presents that methodology, modified for use in seagrass meadow sediment. The first part of the paper discusses the effects of bioturbation, remineralization, allochthonous (non-seagrass-derived) organic carbon, and the formation and burial of inorganic carbon within the meadow. The second part presents a step-by-step method and includes example profiles of 210Pb and organic carbon to help with interpretation in non-ideal sedimentary settings.

IMPORTANT CONSIDERATIONS: BIOTURBATION, REMINERALIZATION, ALLOCHTHONOUS CARBON, AND EFFECT OF CARBONATE

Effects of bioturbation on sediment core profiles

In most parts of the ocean, surface sediment is mixed (bioturbated) by the activities of animals that live in or on the sediment[19]. In the intertidal or shallow subtidal zone, sediment can also be mixed by waves. Bioturbation and wave-mixing result in a surface mixed layer (SML) in most marine sediment. The average depth of the SML globally is 9.8 ± 4.5 cm[19]. Published estimates of SML depth in seagrass meadow sediment are rare, but range from 2-3 cm[20] to 15 cm[21].

Bioturbation or wave mixing affects the profiles of transient tracers in sediment [Figure 1]. It smears multiple years of sedimentation together[22]. For example, in sediment that accumulates at 0.1 cm yr-1, with a 2-3 cm SML[20], 20-30 years of sediment are mixed together. Consequently, it is incorrect to assign a discrete year to a particular depth in a mixed core[23].

How to quantify blue carbon sequestration rates in seagrass meadow sediment: geochemical method and troubleshooting

Figure 1. Effects of bioturbation on tracer profiles in sediment (modified from[4]). Modeled tracer concentration profile that would result after 60 years of sedimentation at 0.25 cm yr-1, with the same initial tracer concentration in both panels: (A) with no bioturbation, and (B) with slow bioturbation (3 cm2 yr-1) within a 7 cm surface mixed layer. Note that the bottom of the tracer pulse reaches 14.5 cm in panel a and 24.5 cm in (B). If a sedimentation rate were calculated based on a known date of entry of the tracer in this mixed sediment, without accounting for mixing, the calculated rate would be 1.7 times too high.

An introduced tracer, such as a layer of feldspar, e.g.[24], would be mixed to a greater depth than it would have reached without mixing. Similarly, 137Cs, which entered the environment in 1954, will be found in most marine sediment at a greater depth than it would have reached in the absence of mixing[23]. Using a tracer without accounting for mixing always overestimates the sedimentation rate[23]. The Appleby[25] Constant Rate of Supply methodology cannot be used to determine a variable sedimentation rate in a mixed core; it is designed only for undisturbed cores, such as those collected in anoxic basins.

Bioturbated cores can be interpreted, but mixing must be taken into account, as described in below.

Carbon remineralization in surface sediment

Bioturbating animals consume some of the organic carbon, remineralizing it to CO2 and reducing the amount available to be buried [Figure 2][26,27]. Remineralization continues below the surface mixed layer (SML) due to the microbial degradation of organic matter. (Microbial remineralization occurs even in the absence of bioturbation). Mixing moves oxygen deeper into the core, which increases the rate of microbial degradation[18].

How to quantify blue carbon sequestration rates in seagrass meadow sediment: geochemical method and troubleshooting

Figure 2. Effect of remineralization on organic carbon profiles in sediment (modified from[4]), with CO2 efflux result from[26]. Organic carbon concentration declines with depth due to microbial remineralization, even in the absence of bioturbation (A). With bioturbation (B), remineralization is rapid and irregular and continues deeper into the core, resulting in a greater reduction in organic carbon burial. In both cases, using the concentration of organic carbon in the top 10 cm would overestimate the rate of carbon burial.

Eventually, the organic carbon is buried to a depth where it only degrades very slowly. This is the effective carbon burial depth[4]. The % organic carbon at the burial depth represents the buried % organic carbon. As illustrated in Figure 2, measuring organic carbon in the top 10 cm, as is commonly the case in blue carbon studies, e.g.,[1,28], would overestimate the amount of carbon buried.

Whether to include allochthonous carbon

The total organic carbon measured in seagrass meadow sediment represents a combination of seagrass carbon and carbon from other sources (allochthonous carbon + phytoplankton). These other sources of carbon include terrigenous material from land runoff, marine-derived material, such as phytoplankton, and organic matter transferred from other nearby blue carbon ecosystems, such as mangroves. There has been some disagreement over whether to include or exclude the allochthonous carbon in the sequestration rate calculated for the seagrass meadow, e.g.,[29]vs.[30].

For the calculation of carbon offset credits, the Voluntary Carbon Standard protocol, VM0033[31], specifies that allochthonous carbon is to be excluded. That can be done using biomarkers, as discussed in Section "Separate seagrass carbon from total organic carbon using biomarkers" below.

Effect of carbonate

Inorganic carbon (e.g., carbonate-rich parts of seagrasses or calcium carbonate shells from associated meiofauna) is often buried along with organic carbon in seagrass meadows[32]. When calcium carbonate is formed, it has the non-intuitive effect of releasing carbon dioxide[33]. At the current pH of seawater, approximately 0.6 moles of CO2 are released for every mole of carbonate formed, and the ratio is expected to increase as seawater pH continues to decline[33]. The burial of inorganic carbon locks in this CO2 release[32].

Consequently, the burial of inorganic carbon that was formed within the meadow offsets some of the organic carbon burial [Figure 3]. Note that if the inorganic carbon buried in the meadow comes from land and is just being moved from one reservoir to the other, there is no offset effect [Figure 3][34].

How to quantify blue carbon sequestration rates in seagrass meadow sediment: geochemical method and troubleshooting

Figure 3. Cartoon representing deposition of seagrass-related and allochthonous organic and inorganic carbon, showing remineralization of organic carbon in surface sediment. Organic C in the deep part of the left-hand profile represents sequestered seagrass organic carbon, which is offset by the burial of inorganic C formed inside the meadow. Allochthonous organic and allochthonous inorganic C are both excluded from the calculation, because neither results from the presence of the seagrass meadow.

STEP-BY-STEP SEDIMENT CARBON BURIAL CALCULATION METHOD

The method is summarized in Table 1 and described below. Steps 1-3 describe a general method for calculating the rate of total organic carbon burial in marine sediment. Steps 4 and 5 present modifications specific to seagrass meadows: determining the proportion of organic carbon derived from the seagrass itself, and accounting for the offset due to the burial of inorganic carbon formed within the meadow.

Table 1

Summary of steps to determine net, additional carbon burial due to seagrass

StepNotes
1. Determine sediment accumulation rate
        Section sediment coreMinimize/quantify compaction; use high enough resolution to identify SML
e.g. 1-cm resolution for ≥ top 10 cm; Coarser (2-5 cm) OK in deeper part of core
        Analyze radioisotopes for dating210Pb in all sections to bottom of core (~40-50 cm); 226Ra or 214Pb in ≥ 3 segments to determine supported 210Pb
        Identify surface mixed layerLayer above the inflection point in the total or excess 210Pb profile
        Determine sedimentation velocity (cm yr-1)From ln(Excess 210Pb) profile below SML and above background
        Convert to sediment accumulation rate (g cm-2 yr-1)Use porosity below SML
2. Determine carbon burial %Plot % organic C vs. depth; find ~ constant value in deep section of core
3. Calculate total organic C burial rateMultiply % buried organic C by sediment accumulation rate
4. Correct for % seagrass C buried, if excluding allochthonous organic CUse biomarkers to i.d. proportion of seagrass carbon; determine % seagrass organic C buried and multiply by accumulation rate
5. Correct for carbonate formed and buried within the meadowSubtract 0.6 moles of organic C for every 1 mole locally-formed inorganic C buried

Determine sediment accumulation rate

Radioactive lead, 210Pb, is produced in the atmosphere from the decay of 222Rn. It sticks to particles, which sink through the water column and settle to the seafloor. 210Pb decays with a half-life of 22.26 years[35]. As sediment accumulates, the older material is buried, leading to a decline in 210Pb activity with depth, which can be used to determine the sedimentation velocity (cm yr-1)[35].

Radioactive decay of radium in the sediment continually produces new 210Pb; this is the supported 210Pb[35]. The supported 210Pb is subtracted from the total 210Pb activity to determine the excess 210Pb, which is the part that, below the surface mixed layer, declines in proportion to the sedimentation velocity[35].

The bottom of the surface mixed layer is usually marked by a change in the slope of the depth profile of total or excess 210Pb [Figure 4A and B][16]. After about five half-lives (~110 years), the excess 210Pb is exhausted. The profile becomes approximately constant with depth, once only the supported 210Pb remains [Figure 4A]. The sedimentation velocity, ws (cm yr-1), is calculated from the slope of the plot of ln(Excess 210Pb)vs. depth (cm-1), below the SML and above the depth where 210Pb reaches background (Equation 1)[16].

How to quantify blue carbon sequestration rates in seagrass meadow sediment: geochemical method and troubleshooting

Figure 4. Example 210Pb profiles. Horizontal dashed lines represent the bottom of the surface mixed layer (SML). Solid lines show the section of each profile to be used for the calculation of the sedimentation velocity. (A) A profile from a deep, coastal basin sediment. (B) A profile from a Zostera marina meadow, showing a deeper, more disturbed SML but clear decay with depth below the SML. (C) A profile where the core is too short or the sediment too disturbed to reach the decay depth, so no sedimentation velocity can be determined. (D) Inverted 210Pb profile near-surface shows that older material has landed on top of newer; a sedimentation velocity can be determined below the slump, but the absolute age of the deep section is unclear. (E) A core with a slump of older material at mid-depth, above which regular accumulation seems to have resumed; SML may or may not be present; this rate would be uncertain relative to those in (A and B).

ws = -0.03114/slope                     (1)

where -0.03114 yr-1 is the decay rate constant of 210Pb. It is important to collect a core that is long enough to see the decay of 210Pb with depth below the SML. In coastal sediment, a ~ 40 cm core is generally long enough. The uppermost section of the core should be sub-sectioned finely enough to identify the SML, e.g., 1-cm intervals for at least the top 10 cm. Deeper intervals can be sub-sectioned at the same or somewhat coarser (2-5 cm) resolution.

The sedimentation velocity is converted to a mass accumulation rate, rs (g cm-2 yr-1), using the porosity, ϕ and the sediment density, ρs (g cm-3) (Equation 2)[16].

rs = ws(1-ϕ)ρs                             (2)

The porosity can be determined from the ratio of dry mass (g) to wet volume (cm-3) in each subsection of the core (Equation 3). (The analytical lab can provide a correction for the mass of salt based on the salinity of the overlying seawater.)

ϕ = 1 - (dry mass/wet volume)ρs-1                  (3)

This requires the measurement or assumption of a sediment density. In sediment that is primarily inorganic, with only a few percent organic C, that can be approximated by the density of quartz sand or clay minerals (2.65 g cm-3); Lavelle et al. (1986) used a measured density of 2.6 g cm-3 in Puget Sound, USA[16]. If the sediment is very organic-rich at a particular site, it would be advisable to measure the density of sediment there.

Troubleshooting 210Pb profiles

210Pb profiles are not always as ideal as those illustrated in Figures 4A and B, particularly in seagrass meadow sediment, which is frequently disturbed by waves and benthic animals. Figure 4 illustrates 210Pb profiles that can result from several non-ideal situations, including when the core is either too short or too disturbed to show the decay with depth [Figure 4C], and where there has been a slump of older material on top of younger, either at the top [Figure 4D] or in the middle [Figure 4E] of a core. Additional, idealized examples are illustrated by Arias-Ortiz et al. (2018)[9].

If there is no detectable Excess 210Pb above background, this indicates that the area is non-depositional or even erosional, and no burial is taking place. In such a situation, there might still be elevated organic carbon in the surface sediment below a seagrass meadow, because bioturbation can mix carbon or other substances down into the sediment, e.g.,[36]. However, if there is no sediment accumulation, then carbon is not actively buried at that site.

It is crucial to exercise caution when calculating sediment accumulation rate, because the rest of the interpretation depends on it.

Determine burial concentration of organic C

The burial % organic carbon can be determined from a depth profile of % organic carbon, based on the value reached in the deeper part of the core, once the organic carbon has stopped declining with depth [Figure 5A].

How to quantify blue carbon sequestration rates in seagrass meadow sediment: geochemical method and troubleshooting

Figure 5. Example organic carbon profiles. Vertical lines mark the burial % organic C. (A) remineralization in upper section overlies buried % C; (B) constant % organic C indicates either a very high sediment accumulation rate or only refractory C at this site; (C) decline from surface to mid-point, with higher values below, indicates a change in the environment - it is unclear whether the % organic C reaches its burial value.

Troubleshooting organic carbon profiles

If the % organic C does not decline at all with depth (in a ~40 cm core), then either the sedimentation rate is so high that there is no time for the carbon to be remineralized before it is buried, or else all the labile carbon has been remineralized before it reached the sediment, and only refractory carbon remains. In either case, the burial % organic C is the constant value [Figure 5B].

If the organic carbon profile shows any shape other than a decline with depth or a constant value, then the sediment has been disturbed in some way, or there has been a change in the depositional environment. For example, a higher % organic C at the bottom [Figure 5C] might indicate a former seagrass meadow that has died, or an old log boom site, e.g.,[37].

Determine burial rate of total organic C

Multiply the sediment accumulation rate determined in Step 1 by the burial % organic carbon determined in Step 2. Do not calculate a different carbon burial rate at each depth in a single core; multiple years are mixed together, often unevenly, and organic carbon is remineralized with depth, even in the absence of mixing. See Section "Carbon remineralization in surface sediment" above.

This is the burial rate of total organic carbon, not of seagrass carbon specifically.

Separate seagrass carbon from total organic carbon using biomarkers

Biomarkers can be used to determine the proportion of the organic carbon that is derived from seagrass. See the discussion of allochthonous carbon above.

Stable isotopes of carbon and nitrogen (δ13C, δ15N) can provide a simple separation of marine-derived and terrigenous organic matter[38]. However, it can be difficult to discriminate among multiple vegetative end-members, such as phytoplankton, seagrass, seaweed, mangrove litter, etc., using only two tracers[38]. Multiple tracers can be more effective[38]. Potential additional tracers include fatty acids, lipids, lignin, eDNA, and stable isotopes of hydrogen[38,39].

Even if step 4 is not practical for cost or other reasons, just following steps 1-3 would result in better estimates of carbon burial rates than those commonly used in blue carbon studies. It would be important in that case to recognize that the rate included the allochthonous carbon as well as the seagrass carbon.

Correct for the offset due to carbonate formation and burial

The reduction in net carbon burial due to the burial of calcium carbonate that was formed in the water column within the meadow varies widely (5%-300%), depending on the environment, e.g.,[34,40]. Unfortunately, the blue carbon community has not settled on a methodology for determining the provenance of buried carbonate[41], so the overall effect of carbonate burial is still an open question. Some authors have determined the balance of carbonate formation, dissolution and burial within a meadow using a mass balance approach[34], and others have made short-term measurements of CO2 exchange above the meadow[40]. However, these methods are not simple to use. If it is not possible to determine the provenance of the inorganic carbon at a particular site, a conservative approach would be to subtract 0.6 moles of carbon for every mole of inorganic carbon buried. This would likely reduce the net burial more than necessary, which would not make a very big difference in sediment with a high organic:inorganic carbon ratio (e.g., ~ 10:1 in a temperate sediment), but could change the calculated net burial into a net release in sediment with a low organic: inorganic ratio (e.g., 1:10 in a tropical meadow).

CONCLUSION

Although carbon burial in seagrass meadows cannot truly offset fossil fuel emissions, expanded organic carbon burial in seagrass meadows could draw down some atmospheric carbon dioxide in the short term (years to hundreds of years). Since there are real regional variations in seagrass species, sedimentary environment, and water properties, the magnitude of this carbon sink varies widely and needs to be assessed separately for each area. The methodology presented here avoids the systematic, high bias of commonly used methods.

It would be useful for future research to use the methodology presented here to determine carbon burial rates in a wide variety of environments with different seagrass species. Those results could then be used to develop appropriate average burial rates for different situations that could be applied on a regional scale.

DECLARATIONS

Acknowledgments

The author thanks Emily Rubidge, Cynthia Wright, and three anonymous reviewers for their insightful comments on an earlier draft of this manuscript. Patricia Kimber prepared the figures.

Authors’ contributions

The author contributed solely to this article.

Availability of data and materials

Not applicable

Financial support and sponsorship

This work was supported by Fisheries and Oceans Canada.

Conflicts of interest

The author declared that there are no conflicts of interest.

Ethical approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Copyright

© His Majesty the King, in Right of Canada (Crown Copyright).

REFERENCES

1. Kennedy H, Beggins J, Duarte CM, et al. Seagrass sediments as a global carbon sink: isotopic constraints. Global Biogeochem Cy 2010;24:GB4026.

2. Herr D, Landis E. Coastal blue carbon ecosystems: opportunities for nationally determined contributions. Gland, Switzerland; Washington DC, USA: IUCN, The Nature Conservancy; 2016, 28p. Available from: https://www.unep.org/resources/policy-and-strategy/coastal-blue-carbon-ecosystems-opportunities-nationally-determined [Last accessed on 26 Sep 2023].

3. Hejnowicz AP, Kennedy H, Rudd MA, Huxham MR. Harnessing the climate mitigation, conservation and poverty alleviation potential of seagrasses: prospects for developing blue carbon initiatives and payment for ecosystem service programmes. Front Mar Sci 2015;2:32.

4. Johannessen SC, Macdonald RW. Geoengineering with seagrasses: is credit due where credit is given? Environ Res Lett 2016;11:113001.

5. Williamson P, Gattuso JP. Carbon removal using coastal blue carbon ecosystems is uncertain and unreliable, with questionable climatic cost-effectiveness. Front Climate 2022;4:853666.

6. Anderson CM, DeFries RS, Litterman R, et al. Natural climate solutions are not enough. Science 2019;363:933-4.

7. Seddon N, Smith A, Smith P, et al. Getting the message right on nature-based solutions to climate change. Glob Chang Biol 2021;27:1518-46.

8. IPCC. 2013 supplement to the 2006 IPCC guidelines for national greenhouse gas inventories. In Hiraishi T, Krug T, Tanabe K, editors. Switzerland: Intergovernmental Panel on Climate Change; 2014. Available from: https://www.ipcc.ch/publication/2013-supplement-to-the-2006-ipcc-guidelines-for-national-greenhouse-gas-inventories-wetlands/ [Last accessed on 26 Sep 2023].

9. Arias-ortiz A, Serrano O, Masqué P, et al. A marine heatwave drives massive losses from the world’s largest seagrass carbon stocks. Nat Clim Chang 2018;8:338-44.

10. Lovelock CE, Reef R. Variable impacts of climate change on blue carbon. One Earth 2020;3:195-211.

11. Lafratta A, Serrano O, Masqué P, et al. Challenges to select suitable habitats and demonstrate ‘additionality’ in Blue Carbon projects: a seagrass case study. Ocean Coast Manag 2020;197:105295.

12. Leiva-Dueñas C, Graversen AEL, Banta GT, et al. Capturing of organic carbon and nitrogen in eelgrass sediments of southern Scandinavia. Limnol Oceanogr 2023;68:631-48.

13. Smeaton C, Barlow NLM, Austin WEN. Coring and compaction: best practice in blue carbon stock and burial estimations. Geoderma 2020;364:114180.

14. Robbins J, Krezoski J, Mozley S. Radioactivity in sediments of the Great Lakes: post-depositional redistribution by deposit-feeding organisms. Earth Planet Sci Lett 1977;36:325-33.

15. Carpenter R, Peterson M, Bennett J. 210Pb-derived sediment accumulation and mixing rates for the greater Puget Sound region. Mar Geol 1985;64:291-312.

16. Lavelle J, Massoth G, Crecelius E. Accumulation rates of recent sediments in puget sound, Washington. Mar Geol 1986;72:59-70.

17. Silverberg N, Nguyen HV, Delibrias G, et al. Radionuclide profiles, sedimentation rates, and bioturbation in modern sediments of the Laurentian trough, gulf-of-st-lawrence. Oceanologica Acta 1986;9:285-90. Available from: https://archimer.ifremer.fr/doc/00110/22116/ [Last accessed on 26 Sep 2023]

18. Hedges JI, Keil RG. Sedimentary organic matter preservation: an assessment and speculative synthesis. Mar Chem 1995;49:81-115.

19. Boudreau BP. Is burial velocity a master parameter for bioturbation? Geochim Cosmochim Acta 1994;58:1243-9.

20. Marbà N, Arias-ortiz A, Masqué P, et al. Impact of seagrass loss and subsequent revegetation on carbon sequestration and stocks. J Ecol 2015;103:296-302.

21. Serrano O, Ruhon R, Lavery PS, et al. Impact of mooring activities on carbon stocks in seagrass meadows. Sci Rep 2016;6:23193.

22. Guinasso Jr NL, Schink DR. Quantitative estimates of biological mixing rates in abyssal sediments. J Geophys Res 1975;80:3032-43.

23. Johannessen SC, Macdonald RW. There is no 1954 in that core! Interpreting sedimentation rates and contaminant trends in marine sediment cores. Mar Pollut Bull 2012;64:675-8.

24. CEC. Greenhouse gas offset methodology criteria for tidal wetland conservation. Montreal, Canada: Commission for Environmental Cooperation; 2014, 36p. Available from: http://www.cec.org/files/documents/publications/11597-greenhouse-gas-offset-methodology-criteria-tidal-wetland-conservation-en.pdf [Last accessed on 26 Sep 2023].

25. Appleby PG, Oldfieldz F. The assessment of 210Pb data from sites with varying sediment accumulation rates. Hydrobiologia 1983;103:29-35.

26. Thomson ACG, Trevathan-Tackett SM, Maher DT, Ralph PJ, Macreadie PI. Bioturbator-stimulated loss of seagrass sediment carbon stocks. Limnol Oceanogr 2019;64:342-56.

27. Stolpovsky K, Dale AW, Wallmann K. Toward a parameterization of global-scale organic carbon mineralization kinetics in surface marine sediments. Global Biogeochem Cy 2015;29:812-29.

28. Greiner JT, McGlathery KJ, Gunnell J, McKee BA. Seagrass restoration enhances "blue carbon" sequestration in coastal waters. PLoS One 2013;8:e72469.

29. Krause JR, Hinojosa-Corona A, Gray AB, et al. Beyond habitat boundaries: organic matter cycling requires a system-wide approach for accurate blue carbon accounting. Limnol Oceanogr 2022;67:S6-18.

30. Gallagher JB, Zhang K, Chuan CH. A Re-evaluation of wetland carbon sink mitigation concepts and measurements: a diagenetic solution. Wetlands 2022;42:23.

31. Emmer I, von Unger M, Needelman B, Crooks S, Emmett-Mattox S. Coastal blue carbon in practice: manual for using the vcs methodology for tidal wetland and seagrass restoration VM0033. In: Simpson S, editor, Arlington: restore America’s estuaries, Silvestrum; 2015, p. 82. Available from: https://estuaries.org/wp-content/uploads/2018/08/rae-coastal-blue-carbon-methodology-web.pdf [Last accessed on 27 Sep 2023]

32. Gullström M, Lyimo LD, Dahl M, et al. Blue carbon storage in tropical seagrass meadows relates to carbonate stock dynamics, plant-sediment processes, and landscape context: insights from the western indian ocean. Ecosystems 2018;21:551-66.

33. Frankignoulle M, Canon C, Gattuso J. Marine calcification as a source of carbon dioxide: positive feedback of increasing atmospheric CO2. Limnol Oceanogr 1994;39:458-62.

34. Saderne V, Geraldi NR, Macreadie PI, et al. Role of carbonate burial in blue carbon budgets. Nat Commun 2019;10:1106.

35. Robbins JA. Geochemical and geophysical applications of radioactive lead. In: the biogeochemistry of lead in the environment. Amsterdam, The Netherlands: Elsevier/North-Holland Biomedical Press; 1978. pp. 285-393.

36. Dinn PM, Johannessen SC, Macdonald RW, Lowe CJ, Whiticar MJ. Effect of receiving environment on the transport and fate of polybrominated diphenyl ethers near two submarine municipal outfalls. Environ Toxicol Chem 2012;31:566-73.

37. Spooner A. Blue carbon sequestration potential in Zostera marina eelgrass beds of the K'omoks Estuary, British Columbia. Master Thesis, Royal Roads University; 2016. Available from: http://hdl.handle.net/10170/916 [Last accessed on 26 Sep 2023].

38. Geraldi NR, Ortega A, Serrano O, et al. Fingerprinting blue carbon: rationale and tools to determine the source of organic carbon in marine depositional environments. Front Mar Sci 2019;6:263.

39. Duarte CM, Delgado-Huertas A, Anton A, et al. Stable isotope (δ13C, δ15N, δ18O, δD) composition and nutrient concentration of red sea primary producers. Front Mar Sci 2018;5:298.

40. Van Dam BR, Zeller MA, Lopes C, et al. Calcification-driven CO2 emissions exceed “Blue Carbon” sequestration in a carbonate seagrass meadow. Sci Adv 2021;7:eabj1372.

41. Macreadie PI, Serrano O, Maher DT, Duarte CM, Beardall J. Addressing calcium carbonate cycling in blue carbon accounting. Limnol Oceanogr Lett 2017;2:195-201.

Cite This Article

Technical Note
Open Access
How to quantify blue carbon sequestration rates in seagrass meadow sediment: geochemical method and troubleshooting
Sophia C. JohannessenSophia C.  Johannessen

How to Cite

Johannessen, S. C. How to quantify blue carbon sequestration rates in seagrass meadow sediment: geochemical method and troubleshooting. Carbon Footprints. 2023, 2, 21. http://dx.doi.org/10.20517/cf.2023.37

Download Citation

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click on download.

Export Citation File:

Type of Import

Tips on Downloading Citation

This feature enables you to download the bibliographic information (also called citation data, header data, or metadata) for the articles on our site.

Citation Manager File Format

Use the radio buttons to choose how to format the bibliographic data you're harvesting. Several citation manager formats are available, including EndNote and BibTex.

Type of Import

If you have citation management software installed on your computer your Web browser should be able to import metadata directly into your reference database.

Direct Import: When the Direct Import option is selected (the default state), a dialogue box will give you the option to Save or Open the downloaded citation data. Choosing Open will either launch your citation manager or give you a choice of applications with which to use the metadata. The Save option saves the file locally for later use.

Indirect Import: When the Indirect Import option is selected, the metadata is displayed and may be copied and pasted as needed.

About This Article

© The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Data & Comments

Data

Views
1487
Downloads
269
Citations
1
Comments
0
11

Comments

Comments must be written in English. Spam, offensive content, impersonation, and private information will not be permitted. If any comment is reported and identified as inappropriate content by OAE staff, the comment will be removed without notice. If you have any queries or need any help, please contact us at support@oaepublish.com.

0
Download PDF
Share This Article
Scan the QR code for reading!
See Updates
Contents
Figures
Related
Carbon Footprints
ISSN 2831-932X (Online)

Portico

All published articles are preserved here permanently

https://www.portico.org/publishers/oae/

Portico

All published articles are preserved here permanently

https://www.portico.org/publishers/oae/