Abstract
Mitigating climate change through the reduction of atmospheric CO2 levels is of interest, particularly through maintaining and re-establishing natural ecosystems that act as carbon sinks, such as coastal vegetated habitats or “blue carbon” systems. Here we compare sedimentary blue carbon (C) stocks from 37 sediment cores collected in pristine (n = 13), agricultural (n = 11), and urban (n = 13) estuaries within the same geomorphological region, located on the eastern coast of Australia. The mean estimated C stocks for each carbon system (seagrass, mangrove, and saltmarshes) were 402 ± 78, 830 ± 109, and 723 ± 100 Mg C ha-1, respectively, conservatively estimated up to 3 m depths. Analysis of variance revealed no significant difference between C stocks per area (C ha-1) considering each habitat type and between specific estuaries. However, the total estuarine C stocks were found to be greater with increasing levels of conservation, based on larger areas of blue carbon vegetation. The potential loss of C to the atmosphere from these small regional estuaries are 500,574 ± 118,635 tons of CO2 equivalent (CO2e), based on specific assumptions. The implication of these results are that there are large C stocks in small regional estuaries which supports the protection of blue C systems in developing coastal areas and highlights the uncertainties of the CO2 emissions from potential blue C habitat degradation.
Introduction
Vegetated coastal ecosystems (i.e., seagrass beds, saltmarsh meadows, and mangrove forests) are highly productive ecosystems that play a critical role in the global carbon, water, and nutrient cycles (; ; ). Their natural ability to sequester substantial amounts of carbon dioxide (CO2) from the atmosphere via the long term burial of carbon in mostly anoxic sediments has become increasingly recognized as important climate change mitigation strategies (; ; ; ; ). However, while these blue C systems are capable of offsetting anthropogenic greenhouse gas emissions through bio- sequestering atmospheric CO2, their continuing decline due to environmental change and human land use activities is reducing their capacity to provide this ecosystem service and ultimately exacerbating global climate change (; ; ).
Over the past several decades, it is estimated that about one third of global mangroves, seagrass, and saltmarsh have been lost as a result of deforestation and habitat reclamation, coastal and urban development, nutrient enrichment, water quality degradation, and climate change (; ; ; ; ; ). This decline in coastal blue C systems still continues today at rates estimated between ∼0.5–3% annually depending on ecosystem type (; ). The degradation of these habitats, particularly the disturbance of sediments, leads to the remineralization of CO2 that has been stored for millennia (; ). An evaluation of global blue carbon emissions emitted as a result of the conversion and degradation of vegetated coastal ecosystems has been estimated at 0.15–1.02 Pg (billion tons) of CO2 being released annually which is estimated to cause economic damages of approximately $US 6–42 billion annually (). These economic damages are associated with restoration efforts in wetlands with ecological benefits and undefined carbon offsets ().
Although there has been an increasing amount of studies focusing on quantifying potential CO2 emissions from blue carbon sediment disturbance to evaluate the effects of habitat loss on greenhouse gas budgets (; ; ; ; ), there are still uncertainties when it comes to variabilities in C stock estimates, particularly in regards to inter-ecosystem variability (; ; ; ; ). While variations in sedimentary carbon stocks in blue C systems have been documented across longitudinal and estuarine spatial gradients (; ; ; ; ), data on the variability of C stocks from blue C systems of the same geomorphological region are scarce.
The current study was therefore undertaken with the objective of (i) estimating and evaluating variability in sedimentary blue carbon stocks of three estuaries within the same geomorphological region and (ii) quantifying possible variability in sedimentary C stocks as a result of regional development. A total of 13 sedimentary C stock estimates were estimated from sediment cores collected from blue C systems within a relatively pristine estuarine catchment, 11 cores from a predominately agricultural impacted estuarine catchment, and 13 sediment cores were collected from an urbanized estuary catchment. For comparative purposes, extrapolations of saltmarsh, mangrove and seagrass sediment C stocks were calculated for each estuary and the potential CO2 emissions from habitat degradation were based on these sedimentary C stock estimates.
Materials and Methods
Study Sites
Field observations were performed along three coastal estuaries on the subtropical East Coast of New South Wales, Australia (Figure 1). The Wooli River, Corindi River, and Coffs Creek estuaries are all tidal estuaries situated within the same geomorphological region (within 50 km of each other) and experience a similar subtropical climate of hot wet summers and cold dry winters. The region receives an average annual rainfall of approximately 1600 mm with the wettest and driest months being February and September, respectively. Each estuary contains all three blue C systems with the dominant species for each blue carbon system being Zostera muelleri (seagrass), Sporobolus virginicus (saltmarsh), and Avicennia marina (mangrove).
FIGURE 1
Although the three estuaries in this study experience a similar climate, they differ in terms of the degree of environmental impact and regional development within their catchments. The estuary situated the furthest north of all estuaries, the Wooli River estuary, is located in the Yuraygir National Park in the Northern Rivers district of New South Wales, Australia (29.89° S, 153.27° E) (Figure 1). The closest villages are Minnie Water, situated at 13.7 km north from the Wooli River, and Red Rock, which is found 48 km south from Wooli. Although in the surroundings of the river there are camping and caravan parks, as well as holiday apartments, the Wooli River is known to be one of the most pristine systems in New South Wales, Australia. The Wooli River estuary has an area of 370 ha and a total catchment area of 18,000 ha.
Also situated in the Northern Rivers district of New South Wales, the Corindi River estuary (29.98° S, 153.23° E) and its surrounding catchment (190 ha) drains to the ocean in the town of Red Rock, NSW (population: 435,
The urban estuary studied in this work, Coffs Creek estuary (30.30° S, 153.14° E), is situated in the northern section of the Mid North Coast near the township of Coffs Harbour, NSW Australia (Figure 1). The estuary has a catchment area of about 250 ha of which 80% is dominated by urban development and agriculture, while just 16% is considered undisturbed (
Sample Collection and C Stock Calculations
Sampling was conducted in March 2016 (Coffs Creek estuary), March 2017 (Corindi River estuary), and March 2018 (Wooli River estuary). Using a 50 cm long, 5 cm diameter Russian Peat auger (mangrove and saltmarsh) or PVC corer with a 7 cm inner diameter (seagrass). Sediment cores were collected, at least two sediment cores in each blue carbon system, along each estuary (Figure 1). At each sampling site, soil depth was measured using a 3 m metal rod to probe for soil bedrock. If the rod became fully submerged in the sediment, a conservative depth of 3 m was presumed. Once collected, sediment cores were sectioned into 2 cm intervals. This sampling protocol is designed to allow maximum spatial coverage, based on available resources, and allowed for comparisons with other blue carbon stock studies that sampled three depth intervals per sediment core (
Dry bulk density (DBD) was calculated for each interval using the dry weight of sediment and volume of sample from the sediment core. Three subsamples from each core (8–10, 28–30, and 48–50 cm) were placed into the oven at 105°C until dry, to obtain the sample dry weight. The three samples per sediment core were then placed in the furnace at 550°C to burn off the organic matter [loss on ignition (L.O.I.)] (
Table 1
| Wooli | Corindi | Coffs | ||
|---|---|---|---|---|
| River (ha) | River (ha) | Creek (ha) | NSW (ha) | |
| Seagrass | 9.4 | 2.4 | 0.2 | 15,900 |
| Mangrove | 86.0 | 37.1 | 20.1 | 12,500 |
| Saltmarsh | 66.9 | 52.7 | 1.4 | 7,200 |
Total area (ha) of each blue carbon ecosystem within Wooli River estuary, Corindi River estuary, and Coffs Creek estuary.
Data Analysis
To evaluate differences in carbon stocks (Mg C ha-1), carbon density (g C cm-3), and carbon content (g C g sediment-1) between locations (Coffs, Corindi, and Wooli; fixed factor), habitat types (seagrass, mangrove, and saltmarsh; fixed factor), and cores (three replicate subsamples; random, nested within location and habitat type), we ran a distance-based multiple factor PERMANOVA on a Euclidian similarity matrix of all samples. We used 9999 permutations of residuals under a reduced model to generate P-values and Type III (partial) sums of squares to account for the unbalanced number of cores in each location. The spatial distribution of carbon stock, carbon density, and carbon content was visualized using a non-metric MDS (multidimensional scaling) scatter plot. All analyses were done using PRIMER 7 (
Results
Below we outline the results for each blue C systems from the Wooli River, Corindi River and Coffs Creek estuaries individually. Sedimentary blue carbon stock data for Coffs Creek estuary are summarized from
Wooli River Estuary
Seagrass
Carbon content (percentage C of total sample dry weight) in the seagrass sediment samples from the Wooli River estuary ranged from 0.75 to 0.96% with an average of 0.85 ± 0.11% (Table 2). The dry bulk densities (DBD) ranged from 1.48 to 1.55 g cm-3 with an average DBD of 1.51 ± 0.06 g cm-3. From these, sedimentary seagrass carbon stocks were estimated between 348 and 391 Mg C ha-1, with an overall average of 371 ± 31 Mg C ha-1.
Table 2
| Study site | Habitat and location | Depth (cm) | Carbon content (%) | Dry bulk density (g cm-3) | Carbon stock (Mg C ha-1) |
|---|---|---|---|---|---|
| Wooli River | Seagrass site 1 | 300 | 0.96 ± 0.37 | 1.48 ± 0.17 | 390.65 ± 98.58 |
| Seagrass site 2 | 300 | 0.75 ± 0.02 | 1.55 ± 0.12 | 348.09 ± 34.76 | |
| Seagrass site 3 | 300 | 0.84 ± 0.04 | 1.48 ± 0.05 | 374.83 ± 11.46 | |
| Seagrass average | 300 ± 0 | 0.85 ± 0.11 | 1.51 ± 0.06 | 371.19 ± 30.99 | |
| Mangrove site 1 | 122 | 1.45 ± 0.51 | 1.09 ± 0.06 | 186.50 ± 58.57 | |
| Mangrove site 3 | 219 | 2.98 ± 1.10 | 0.96 ± 0.15 | 560.87 ± 161.96 | |
| Mangrove site 4R | 300 | 2.10 ± 0.41 | 1.00 ± 0.05 | 641.46 ± 158.58 | |
| Mangrove site 4A | 300 | 2.18 ± 0.23 | 0.86 ± 0.10 | 545.61 ± 4.96 | |
| Mangrove site 5 | 300 | 5.11 ± 0.84 | 0.90 ± 0.17 | 1332.22 ± 185.45 | |
| Mangrove average | 248 ± 18 | 2.76 ± 0.37 | 0.96 ± 0.05 | 642.64 ± 93.61 | |
| Saltmarsh site 1 | 97 | 5.53 ± 1.89 | 1.26 ± 0.07 | 690.86 ± 264.73 | |
| Saltmarsh site 3 | 166 | 8.42 ± 1.18 | 0.48 ± 0.03 | 678.32 ± 121.73 | |
| Saltmarsh site 5 | 300 | 3.78 ± 1.33 | 1.32 ± 0.24 | 1326.01 ± 366.60 | |
| Saltmarsh average | 187 ± 28 | 5.91 ± 1.01 | 1.02 ± 0.15 | 898.39 ± 172.36 | |
| Coridni River | Seagrass site 1 | 110 | 0.78 ± 0.06 | 1.18 ± 0.08 | 101.74 ± 13.52 |
| Seagrass site 2 | 300 | 2.33 ± 1.53 | 1.33 ± 0.08 | 944.34 ± 628.42 | |
| Seagrass average | 205 ± 95 | 1.55 ± 0.77 | 1.26 ± 0.06 | 523.04 ± 338.40 | |
| Mangrove site 1 | 300 | 4.09 ± 0.73 | 0.59 ± 0.05 | 740.90 ± 175.65 | |
| Mangrove site 2 | 300 | 5.86 ± 0.93 | 0.81 ± 0.07 | 1438.85 ± 319.16 | |
| Mangrove site 3 | 300 | 2.04 ± 0.26 | 1.00 ± 0.12 | 603.78 ± 67.12 | |
| Mangrove site 4 | 135 | 4.42 ± 0.07 | 0.82 ± 0.11 | 490.02 ± 57.17 | |
| Mangrove site 5 (upper tidal) | 240 | 3.69 ± 1.65 | 0.88 ± 0.15 | 689.32 ± 219.60 | |
| Mangrove site 5 (lower tidal) | 245 | 2.64 ± 0.66 | 0.75 ± 0.06 | 469.20 ± 79.14 | |
| Mangrove average | 253 ± 26 | 3.81 ± 0.43 | 0.79 ± 0.05 | 738.72 ± 100.74 | |
| Saltmarsh site 1 | 300 | 20.62 ± 11.45 | 0.45 ± 0.25 | 1102.40 ± 470.78 | |
| Saltmarsh site 2 | 170 | 1.43 ± 0.16 | 0.98 ± 0.04 | 242.28 ± 46.84 | |
| Saltmarsh site 3 | 300 | 1.38 ± 0.33 | 0.95 ± 0.13 | 386.67 ± 86.02 | |
| Saltmarsh site 4 | 150 | 3.15 ± 1.63 | 0.90 ± 0.19 | 345.90 ± 104.67 | |
| Saltmarsh site 5 | 85 | 1.67 ± 0.35 | 1.06 ± 0.07 | 149.65 ± 31.05 | |
| Saltmarsh average | 201 ± 43 | 5.65 ± 2.80 | 0.87 ± 0.08 | 445.38 ± 123.06 | |
| Coffs Creek | Seagrass site 1 (middle of patch) | 228 | 2.28 ± 0.56 | 1.18 ± 0.11 | 588.65 |
| Seagrass site 1 (middle of patch) | 228 | 1.81 ± 0.18 | 1.27 ± 0.06 | 522.49 | |
| Seagrass site 2 | 210 | 0.73 ± 0.47 | 1.56 ± 0.17 | 223.26 | |
| Seagrass site 3 | 300 | 0.22 ± 0.05 | 1.86 ± 0.12 | 125.94 | |
| Seagrass average | 242 ± 20 | 1.26 ± 0.48 | 1.47 ± 0.15 | 365.09 ± 112.57 | |
| Mangrove site 1 (upper tidal) | 300 | 1.33 ± 0.52 | 0.71 ± 0.13 | 282.72 ± 134.96 | |
| Mangrove site 1 (lower tidal) | 300 | 5.20 ± 0.95 | 0.55 ± 0.10 | 802.18 ± 27.26 | |
| Mangrove site 2 (upper tidal) | 300 | 4.46 ± 2.65 | 1.52 ± 0.08 | 2104.16 ± 1272.18 | |
| Mangrove site 2 (lower tidal) | 300 | 1.23 ± 0.36 | 0.99 ± 0.33 | 354.54 ± 186.31 | |
| Mangrove site 3 (upper tidal) | 300 | 3.07 ± 1.37 | 0.92 ± 0.20 | 684.27 ± 110.71 | |
| Mangrove site 3 (lower tidal) | 300 | 9.70 ± 5.38 | 1.03 ± 0.29 | 2191.00 ± 571.18 | |
| Mangrove average | 300 ± 0 | 4.16 ± 1.29 | 0.95 ± 0.14 | 1069.81 ± 350.16 | |
| Saltmarsh site 1 | 248 | 4.67 ± 1.67 | 1.02 ± 0.24 | 1111.87 ± 342.21 | |
| Saltmarsh site 2 | 180 | 6.97 ± 2.34 | 0.78 ± 0.25 | 861.00 ± 332.54 | |
| Saltmarsh site 3 | 300 | 5.22 ± 1.94 | 0.62 ± 0.10 | 740.18 ± 0.95 | |
| Saltmarsh average | 243 ± 35 | 5.62 ± 1.05 | 0.81 ± 0.12 | 904.35 ± 109.47 | |
Depth (cm), C content (%), dry bulk density (g cm-3), and C stocks (Mg C ha-1) for seagrass, mangrove, and saltmarsh cores collected from Wooli and Corindi River estuaries.
Coffs Creek estuary data can be found in
Mangrove
Carbon content in the mangrove sediment samples from the Wooli River estuary ranged from 1.45 to 5.11% with an average of 2.76 ± 0.37% (Table 2). The DBD ranged from 0.86 to 1.09 g cm-3 with an average DBD of 0.96 ± 0.05 g cm-3. From these, sedimentary mangrove carbon stocks were estimated between 187 and 1332 Mg C ha-1, with an overall average of 642 ± 94 Mg C ha-1.
Saltmarsh
Carbon content in the saltmarsh sediment samples from the Wooli River estuary ranged from 3.78 to 8.42% with an average of 5.91 ± 1.01% (Table 2). The DBD ranged from 0.48 to 1.32 g cm-3 with an average DBD of 1.02 ± 0.15 g cm-3. From these, sedimentary saltmarsh carbon stocks were estimated between 678 and 1326 Mg C ha-1, with an overall average of 898 ± 172 Mg C ha-1.
Corindi River Estuary
Seagrass
Carbon content in the seagrass sediment samples ranged from 0.78 to 2.33% with an average of 1.55 ± 0.77% (Table 2). The DBD ranged from 1.18 to 1.33 g cm-3 with an average DBD of 1.26 ± 0.06 g cm-3. From these, sedimentary seagrass carbon stocks were estimated between 102 and 944 Mg C ha-1, with an average of 523 ± 338 Mg C ha-1.
Mangrove
Carbon content in the mangrove sediment samples ranged from 2.04 to 5.86% with an average of 3.81 ± 0.43% (Table 2). The DBD ranged from 0.59 to 1.00 g cm-3 with an average DBD of 0.79 ± 0.05 g cm-3. From these, sedimentary mangrove carbon stocks were estimated between 469 and 1439 Mg C ha-1 with an average of 739 ± 101 Mg C ha-1.
Saltmarsh
Carbon content in the saltmarsh sediment samples ranged from 1.38 to 20.62% with an average of 5.65 ± 2.80% (Table 2). The DBD ranged from 0.45 to 1.06 g cm-3 with an average DBD of 0.87 ± 0.08 g cm-3. From these, sedimentary saltmarsh carbon stock estimates were estimated between 150 and 1102 Mg C ha-1 with an average of 445 ± 123 Mg C ha-1.
Coffs Creek Estuary
Seagrass
Carbon content in the seagrass sediment samples ranged from 0.22 to 2.28% with an average of 1.26 ± 0.48% (Table 2). The DBD ranged from 1.18 to 1.86 g cm-3 with an average DBD of 1.47 ± 0.15 g cm-3. From these, sedimentary seagrass carbon stocks were estimated between 126 and 589 Mg C ha-1, with an average of 365 ± 113 Mg C ha-1.
Mangrove
Carbon content in the mangrove sediment samples ranged from 1.23 to 9.70% with an average of 4.17 ± 1.29% (Table 2). The DBD ranged from 0.55 to 1.52 g cm-3 with an average DBD of 0.95 ± 0.14 g cm-3. From these, sedimentary mangrove carbon stocks were estimated between 283 and 2191 Mg C ha-1 with an average of 1070 ± 350 Mg C ha-1.
Saltmarsh
Carbon content in the saltmarsh sediment samples ranged from 4.67 to 6.97% with an average of 5.62 ± 1.05% (Table 2). The DBD ranged from 0.62 to 1.02 g cm-3 with an average DBD of 0.81 ± 0.12 g cm-3. From these, sedimentary saltmarsh carbon stock estimates were estimated between 740 and 1112 Mg C ha-1 with an average of 904 ± 109 Mg C ha-1.
Statistical Analysis
Despite the variabilities in sedimentary C stocks observed within and between estuaries (Table 3), the results of the PERMANOVA revealed no significant interaction between C stock per unit area, C density or C content between locations (p = 0.46, pseudo-F = 0.79), habitats (p = 0.15, pseudo-F = 2.10), or habitat amongst locations (p = 0.55, pseudo-F = 0.77). There was however, a significant difference among replicates (cores) within each habitat and location (p = 0.004, pseudo-F = 2.30) (Table 3). Differences in C stock, C density and C content among cores within the same habitat and location were responsible for the greatest components of variation (Table 3). All results however, must be interpreted with caution as sample size within locations and habitats was relatively low.
Table 3
| Source | Estimate of component of variation | Sq. root |
|---|---|---|
| Habitat | 22325 | 149.42 |
| Location | -4395.4 | -66.298 |
| Habitat × location | -13975 | -118.22 |
| Replicates | 1.2956E+05 | 359.94 |
| Residual | 2.9818E+05 | 546.06 |
Estimates of components of variation from PERMANOVA.
Discussion
Variabilities in Sedimentary Blue Carbon Stocks
Global averages indicate that mangroves systems have generally higher sedimentary organic C densities than any other blue carbon system (
FIGURE 2

Carbon stocks (Mg C ha-1) of the urbanized Coffs Creek estuary (white), the agriculturally impacted Corindi River estuary (gray) and the pristine Wooli River estuary (black). Data are presented in means while bars represent standard errors. Analysis of variance found no significant differences between habitat type or location.
The results here suggest that the various degrees of development across the three estuaries in this study had no significant influence on C stocks per unit area among each blue carbon system. There was however, a significant difference among replicate C stock estimates within each blue carbon system in each estuary; suggesting that local conditions may influence the variabilities more so than regional scale processes. Local scale conditions such as elevation and subsequent tidal inundation, geomorphic location within the estuary, and proximity to allochthonous carbon sources as well as nutrient inputs have been identified in the literature to be major drivers of sedimentary blue carbon stock variabilities (
FIGURE 3

Negative relation between organic carbon content (%) and dry bulk density (g cm-3 year-1) from the sediment core intervals of this work.
The sedimentary C stock data from this study adds to the growing understanding of regional C storage in coastal blue carbon systems. While we have shown C stocks per area in seagrass, mangroves and saltmarsh sediments to be similar in subtropical estuaries with various stages of development (Figure 2), the effects of development itself on the areal extent of these systems can have severe consequences in regards to the total C stored within an estuary. For instance, the areal extent of each blue carbon system identified in Table 1 decreased with increasing development across the three estuaries (i.e., from the relatively pristine Wooli River estuary through to the sparsely developed Corindi River estuary and severely urbanized Coffs Creek estuary). Subsequently, the decreased areal extent of each blue carbon system resulted in the observed decrease in total C stocks with increasing development across the three estuaries (Figure 4).
FIGURE 4

Total carbon stock estimates for seagrass, mangrove and saltmarsh in Coffs Creek (white), Corindi estuary (gray), and Wooli estuary (black) (Mg C). Error bars indicate the standard error.
Another important influence on coastal habitat area between the three estuaries may be related to water quality. Greater urban development has led to elevated suspended sediment and nutrient concentrations in Coffs Creek (
Potential Blue Carbon Emissions From Regional Development
Based on the average sedimentary carbon stocks for each blue carbon ecosystems in this study, and combined with the monetary value of carbon at a price of $AUD 12.14 per Mg, established by the Australian Emissions Reduction Fund auctions (ERF), it is estimated that over $AUD 2.35 ± 0.59 million worth of carbon could be stored within the top 3 m of sediments of the three small estuaries in this study alone (Table 4). Despite the similar C stocks per unit area between the three studied estuaries, the blue C systems of the relatively pristine Wooli River estuary are responsible for 61.3% of this monetary value, followed by the agriculturally developed Corindi River estuary (26.9%) and urbanized Coffs Creek estuary (11.8%). The greater areal extent of all three blue C systems in the Wooli River and to a lesser extent the Corindi River estuary allow for higher total C stocks as opposed to the urbanized Coffs Creek Estuary in which blue carbon system expansion or migration is limited along the estuary.
Table 4
| Study site | Blue carbon system | Total C stock (Mg C) | Monetary value ($AUD) | Approximate emissions from top 30 cm of sediment (Mg CO2 eq) | Approximate emissions from top 100 cm of sediment (Mg CO2 eq) | ||||
|---|---|---|---|---|---|---|---|---|---|
| 43% loss | 50% loss | 90% loss | 43% loss | 50% loss to 30 cm then 25% loss to 1 m | 90% loss | ||||
| Wooli River estuary | Seagrass | 3,489 ± 291 | 42,359 ± 3,536 | 551 ± 46 | 640 ± 53 | 1152 ± 96 | 1,835 ± 153 | 648 ± 54 | 3,842 ± 321 |
| Mangrove | 55,267 ± 8,050 | 670,943 ± 97,733 | 10,550 ± 1,537 | 12,268 ± 1,787 | 22,082 ± 3,217 | 35,168 ± 5,123 | 12,411 ± 1,808 | 73,608 ± 10,722 | |
| Saltmarsh | 60,103 ± 11,531 | 729,646 ± 139,982 | 15,216 ± 2,919 | 17,693 ± 3,394 | 31,848 ± 6,110 | 50,721 ± 9,731 | 17,900 ± 3,434 | 106,160 ± 20,367 | |
| Total | 118,859 ± 19,872 | 1,442,949 ± 241,251 | 26,317 ± 4,502 | 30,602 ± 5,235 | 55,083 ± 9,423 | 87,724 ± 15,007 | 30,959 ± 5,296 | 183,609 ± 31,409 | |
| Corindi River estuary | Seagrass | 1,255 ± 812 | 15,239 ± 9,860 | 290 ± 188 | 337 ± 218 | 607 ± 393 | 966 ± 625 | 341 ± 221 | 2,023 ± 1,309 |
| Mangrove | 27,406 ± 3,738 | 332,713 ± 45,373 | 5,128 ± 699 | 5,963 ± 813 | 10,734 ± 1,464 | 17,095 ± 2,331 | 6,033 ± 823 | 35,780 ± 4,879 | |
| Saltmarsh | 23,471 ± 6,485 | 284,943 ± 78,730 | 5,528 ± 1,527 | 6,428 ± 1,776 | 11,571 ± 3,197 | 18,428 ± 5,092 | 6,503 ± 1,797 | 38,570 ± 10,657 | |
| Total | 52,133 ± 11,035 | 632,896 ± 133,963 | 10,947 ± 2,414 | 12,729 ± 2,807 | 22,912 ± 5,053 | 36,489 ± 8,048 | 12,877 ± 2,840 | 76,373 ± 16,845 | |
| Coffs Creek estuary | Seagrass | 73 ± 45 | 886 ± 547 | 14 ± 9 | 17 ± 10 | 30 ± 18 | 48 ± 29 | 17 ± 10 | 100 ± 62 |
| Mangrove | 21,503 ± 17,240 | 261,049 ± 209,293 | 3,393 ± 2,721 | 3,946 ± 3,164 | 7,103 ± 5,694 | 11,311 ± 9,069 | 3,992 ± 3,200 | 23,675 ± 18,981 | |
| Saltmarsh | 1,266 ± 265 | 15,370 ± 3,222 | 247 ± 52 | 287 ± 60 | 517 ± 108 | 823 ± 173 | 291 ± 61 | 1,723 ± 361 | |
| Total | 22,842 ± 17,550 | 277,305 ± 213,062 | 3,655 ± 2,781 | 4,250 ± 3,234 | 7,649 ± 5,821 | 12,182 ± 9,271 | 4,299 ± 3,272 | 25,498 ± 19,404 | |
| Total | Seagrass | 4,818 ± 1,148 | 58,485 ± 13,942 | 855 ± 242 | 994 ± 282 | 1,789 ± 507 | 2,849 ± 808 | 1,006 ± 285 | 5,964 ± 1,691 |
| Mangrove | 104,177 ± 29,028 | 1,264,705 ± 352,400 | 19,072 ± 4,957 | 22,177 ± 5,764 | 39,919 ± 10,375 | 63,574 ± 16,523 | 22,436 ± 5,831 | 133,063 ± 34,583 | |
| Saltmarsh | 84,840 ± 18,281 | 1,029,960 ± 221,934 | 20.992 ± 4,499 | 24,409 ± 5,231 | 43,936 ± 9,415 | 69,972 ± 14,995 | 24,694 ± 5,292 | 146,453 ± 31,385 | |
| Total | 193,834 ± 48,458 | 2,353,150 ± 588,276 | 40,919 ± 47,580 | 47,580 ± 11,276 | 85,644 ± 20,298 | 136,396 ± 32,326 | 48,135 ± 11,408 | 285,480 ± 67,658 | |
Total C stock values from each blue C system in this study and associatedmonetary values as well as potential CO2 emissions.
The bold values are averages.
Quantifying the emissions potential (often measured in carbon dioxide equivalent, or CO2e) of potentially remineralized C as a result of regional development and land use change is an important step toward protecting these systems and understanding these anthropogenic impacts on greenhouse gas forcing (
Conclusion
Sediment cores from seagrass, mangrove, and saltmarsh habitats revealed high variability and similarity in organic carbon stocks of a nearly pristine Wooli River estuary as compared to the nearby agriculturally developed Corindi River estuary and urbanized Coffs Creek estuary. These results indicate similar C stocks per area between the three locations within the same region (within 50 km). Furthermore, even though the total carbon stocks decrease with increasing development, information in terms of loss of vegetated area as a result of land use change is not available, which would be important to consider for comparative purposes between each estuary studied and the effects of development. Based on the assumptions outlined in this manuscript, the relatively small regional estuaries have potential emissions of 500,574 ± 118,635 tons of CO2e. This study highlights that the presence of more vegetation due to less development provides a greater area for C storage by incremental increases in total estuary sedimentary blue carbon stocks. However, urban blue C habitats (such as Coffs Creek) and agriculturally impacted blue C habitats (such as Corindi) also have the potential to continue providing valuable ecosystem services. Therefore, the conservation and restoration of blue C habitats in both urban and less developed estuaries are justified to maximize organic C sequestration and reduce atmospheric C emissions.
Statements
Author contributions
All authors did the field work and wrote the manuscript.
Funding
This study is was conducted as the field work component of the course “Frontiers in Marine Science I – Biological Systems and Management” at Southern Cross University, National Marine Science Center in 2017 and 2018. CJS was supported by the Australian Research Council (DE160100443) and PGA was supported by a “la Caixa” Fellowship for post-graduate studies.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmars.2018.00518/full#supplementary-material
References
1
ABS (2016). Census of Population and Housing.Canberra, ACT: Australian Bureau of Statistics.
2
AlongiD. M. (2002). Present state and future of the world’s mangrove forests.Environ. Conserv.29331–349. 10.1017/S0376892902000231
3
AndersonM. J. (2008). Animal-sediment relationships re-visited: characterising species’ distributions along an environmental gradient using canonical analysis and quantile regression splines.J. Exp. Mar. Biol. Ecol.36616–27, 10.1016/j.jembe.2008.07.006
4
AtwoodT. B.ConnollyR. M.AlmahasheerH.CarnellP. E.DuarteC. M.LewisC. J. E.et al (2017). Global patterns in mangrove soil carbon stocks and losses.Nat. Clim. Chang.7523–528. 10.1038/nclimate3326
5
BeaumontN. J.JonesL.GarbuttA.HansomJ. D.TobermanM. (2014). The value of carbon sequestration and storage in coastal habitats.Estuar. Coast. Shelf Sci.13732–40. 10.1016/j.ecss.2013.11.022
6
BrownD. R.ConradS.AkkermanK.FairfaxS.FredericksJ.HanrioE.et al (2016). Seagrass, mangrove and saltmarsh sedimentary carbon stocks in an urban estuary; Coffs Harbour, Australia.Reg. Stud. Mar. Sci.11–6. 10.1016/j.rsma.2016.08.005
7
BurkholderJ. M.TomaskoD. A.TouchetteB. W. (2007). Seagrasses and eutrophication.J. Exp. Mar. Biol. Ecol.35046–72. 10.1016/j.jembe.2007.06.024
8
ChmuraG. L.AnisfeldS. C.CahoonD. R.LynchJ. C. (2003). Global carbon sequestration in tidal, saline wetland soils.Glob. Biogeochem. Cycles17:1111. 10.13227/j.hjkx.2016.06.049
9
ClarkeK. R.GorleyR. N. (2015). Getting Started with PRIMER v7. PRIMER-EPlymouth.
10
ConradS. R.SandersC. J.SantosI. R.WhiteS. A. (2018). Investigating water quality in Coffs coastal estuaries and the relationship to adjacent land use. Part 1: Sediments. National Marine Science Centre, Southern Cross University, Coffs Harbour, NSW, 42.
11
DuarteC. M.LosadaI. J.HendriksI. E.MazarrasaI. and MarbàN. (2013). The role of coastal plant communities for climate change mitigation and adaptation.Nat. Clim. Chang.3961–968. 10.1038/nclimate1970
12
DonatoD. C.KauffmanJ. B.MurdiyarsoD.KurniantoS.StidhamM.KanninenM. (2011). Mangroves among the most carbon-rich forests in the tropics.Nat. Geosci.4293–297. 10.1038/ngeo1123
13
FriessD. A.WebbE. L. (2014). Variability in mangrove change estimates and implications for the assessment of ecosystem service provision.Glob. Ecol. Biogeogr.23715–725. 10.1111/geb.12140
14
GedanK. B.SillimanB.BertnessM. (2009). Centuries of human-driven change in salt marsh ecosystems.Mar. Sci.1117–141. 10.1146/annurev.marine.010908.163930
15
HayesM. A.JesseA.HawkeB.BaldockJ.TabetB.LockingtonD.et al (2017). Dynamics of sediment carbon stocks across intertidal wetland habitats of Moreton Bay, Australia.Glob. Chang. Biol.234222–4234. 10.1111/gcb.13722
16
HopkinsonC. S.CaiW.-J.HuX. (2012). Carbon sequestration in wetland dominated coastal systems — a global sink of rapidly diminishing magnitude.Curr. Opin. Environ. Sustain.4186–194. 10.1016/j.cosust.2012.03.005
17
HowardJ.McleodE.ThomasS.EastwoodE.FoxM.WenzelL.et al (2017). The potential to integrate blue carbon into MPA design and management.Aquat. Conserv.27100–115. 10.1002/aqc.2809
18
IrvingA. D.ConnellS. D.RussellB. D. (2011). Restoring coastal plants to improve global carbon storage: reaping what we sow.PLoS One6:e18311. 10.1371/journal.pone.0018311
19
KellewayJ.SerranoO.BaldockJ.CannardT.LaveryP.LovelockC.et al (2017). Technical Review of Opportunities for Including Blue Carbon in the Australian Government’s Emissions Reduction Fund.Canberra, ACT: CSIRO.
20
LaveryP. S.MateoM. -ÁSerranoO.RozaimiM. (2013). Variability in the carbon storage of seagrass habitats and its implications for global estimates of blue carbon ecosystem service.PLoS One8:e73748. 10.1371/journal.pone.0073748
21
LewisC. J. E.CarnellP. E.SandermanJ.BaldockJ. A.MacreadieP. I. (2017). Variability and vulnerability of coastal ‘blue carbon’stocks: a case study from Southeast Australia.Ecosystems21263–279. 10.1007/s10021-017-0150-z
22
LovelockC. E.AtwoodT.BaldockJ.DuarteC. M.HickeyS.LaveryP. S.et al (2017). Assessing the risk of carbon dioxide emissions from blue carbon ecosystems.Front. Ecol. Environ.15:257–265. 10.1002/fee.1491
23
LovelockC. E.CahoonD. R.FriessD. A.GuntenspergenG. R.KraussK. W.ReefR.et al (2015). The vulnerability of Indo-Pacific mangrove forests to sea-level rise.Nature526559–563. 10.1038/nature15538
24
MacreadieP. I.NielsenD. A.KellewayJ. J.AtwoodT. B.SeymourJ. R.PetrouK.et al (2017a). Can we manage coastal ecosystems to sequester more blue carbon?Front. Ecol. Environ.15206–213. 10.1002/fee.1484
25
MacreadieP. I.OllivierQ.KellewayJ.SerranoO.CarnellP.LewisC. E.et al (2017b). Carbon sequestration by Australian tidal marshes.Sci. Rep.7:44071. 10.1038/srep44071
26
MaherD. T.CallM.SantosI. R.SandersC. J. (2018). Beyond burial: lateral exchange is a significant atmospheric carbon sink in mangrove forests.Biol. Lett.14:20180200. 10.1098/rsbl.2018.0200
27
McLeodE.ChmuraG. L.BouillonS.SalmR.BjörkM.DuarteC. M.et al (2011). A blueprint for blue carbon: toward an improved understanding of the role of vegetated coastal habitats in sequestering CO 2.Front. Ecol. Environ.9552–560. 10.1890/110004
28
MorrisJ. T.BarberD. C.CallawayJ. C.ChambersR.HagenS. C.HopkinsonC. S.et al (2016). Contributions of organic and inorganic matter to sediment volume and accretion in tidal wetlands at steady state.Earth’s Future4110–121. 10.1002/2015EF000334
29
MurrayB. C.PendletonL.JenkinsW. A.SifleetS. (2011). Green Payments for Blue carbon: Economic Incentives for Protecting Threatened Coastal Habitats.Durham: Nicholas Institute for Environmental Policy Solutions.
30
OrthR. J.CarruthersT. J.DennisonW. C.DuarteC. M.FourqureanJ. W.HeckK. L.et al (2006). A global crisis for seagrass ecosystems.AIBS Bull.56987–996. 10.1641/0006-3568(2006)56[987:AGCFSE]2.0.CO;2
31
PendletonL.DonatoD. C.MurrayB. C.CrooksS.JenkinsW. A.SifleetS.et al (2012). Estimating global “blue carbon” emissions from conversion and degradation of vegetated coastal ecosystems.PLoS One7:e43542. 10.1371/journal.pone.0043542
32
RicartA. M.YorkP. H.RasheedM. A.PérezM.RomeroJ.BryantC. V.et al (2015). Variability of sedimentary organic carbon in patchy seagrass landscapes.Mar. Pollut. Bull.100476–482. 10.1016/j.marpolbul.2015.09.032
33
RoperT.CreeseB.ScanesP.StephensK.WilliamsR.Dela-CruzJ.et al (2011). “Assessing the condition of estuaries and coastal lake ecosystems,” in NSW Monitoring, Evaluation and Reporting Program, (Sydney: Office of Environment and Heritage).
34
RyderD.BurnsA.VealR.SchmidtJ.RobertsonM.StewartM.et al (2012). Coffs Creek Estuary Coastal Zone Management Plan Literature and Information Review, ed.HeritageO. O. E. A. (Coffs Harbour, NSW: Coffs Harbour City Council).
35
RyderD.VealR.SbrocchiC.SchmidtJ. (2011). Bellinger-Kalang Rivers EcohealthProject: Assessment of River and Estuarine Condition 2009-2010.Bellingen, NSW: Bellingen Shire Council.
36
SandersC. J.EyreB. D.SantosI. R.MachadoW.Luiz-SilvaW.SmoakJ. M.et al (2014). Elevated rates of organic carbon, nitrogen, and phosphorus accumulation in a highly impacted mangrove wetland.Geophys. Res. Lett.412475–2480. 10.1002/2014GL059789
37
SandersC. J.MaherD. T.TaitD. R.WilliamsD.HollowayC.SippoJ. Z.et al (2016). Are global mangrove carbon stocks driven by rainfall?J. Geophys. Res.1212600–2609. 10.1002/2016JG003510
38
SandersC. J.SmoakJ. M.WatersM. N.SandersL. M.BrandiniN.PatchineelamS. R. (2012). Organic matter content and particle size modifications in mangrove sediments as responses to sea level rise.Mar. Environ. Res.77150–155. 10.1016/j.marenvres.2012.02.004
Summary
Keywords
soil carbon stocks, seagrass, mangrove, saltmarsh, estuaries, Australia
Citation
Conrad S, Brown DR, Alvarez PG, Bates B, Ibrahim N, Reid A, Monteiro LS, Silva DA, Mamo LT, Bowtell JR, Lin HA, Tolentino NL and Sanders CJ (2019) Does Regional Development Influence Sedimentary Blue Carbon Stocks? A Case Study From Three Australian Estuaries. Front. Mar. Sci. 5:518. doi: 10.3389/fmars.2018.00518
Received
13 October 2018
Accepted
21 December 2018
Published
14 January 2019
Volume
5 - 2018
Edited by
Vanessa F. Fonseca, Center for Marine and Environmental Sciences (MARE), Portugal
Reviewed by
Alice R. Jones, University of Adelaide, Australia; Jongseong Ryu, Anyang University, South Korea
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Copyright
© 2019 Conrad, Brown, Alvarez, Bates, Ibrahim, Reid, Monteiro, Silva, Mamo, Bowtell, Lin, Tolentino and Sanders.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Christian Joshua Sanders, christian.sanders@scu.edu.au
†These authors have contributed equally to this work
This article was submitted to Marine Pollution, a section of the journal Frontiers in Marine Science
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