Southeast Asian peatlands supply ∼10 % of the global flux of dissolved organic carbon (DOC) from land to the ocean, but the biogeochemical cycling of this peat-derived DOC in coastal environments is still poorly understood. Here, we use fluorescence spectroscopy and parallel factor (PARAFAC) analysis to distinguish different fractions of dissolved organic matter (DOM) in peat-draining rivers, estuaries and coastal waters of Sarawak, Borneo. The terrigenous fractions showed high concentrations at freshwater stations within the rivers, and conservative mixing with seawater across the estuaries. The autochthonous DOM fraction, in contrast, showed low concentrations throughout our study area at all salinities. The DOM pool was also characterized by a high degree of humification in all rivers and estuaries up to salinities of 25. These results indicate a predominantly terrestrial origin of the riverine DOM pool. Only at salinities > 25 did we observe an increase in the proportion of autochthonous relative to terrestrial DOM. Natural sunlight exposure experiments with river water and seawater showed high photolability of the terrigenous DOM fractions, suggesting that photodegradation may account for the observed changes in the DOM composition in coastal waters. Nevertheless, based on our fluorescence data, we estimate that at least 20 %–25 % of the DOC at even our most marine stations (salinity > 31) was terrestrial in origin, indicating that peatlands likely play an important role in the carbon biogeochemistry of Southeast Asian shelf seas.
River outgassing has proven to be an integral part of the carbon cycle. In Southeast Asia, river outgassing quantities are uncertain due to lack of measured data. Here we investigate six rivers in Indonesia and Malaysia, during five expeditions. CO2 fluxes from Southeast Asian rivers amount to 66.9±15.7 Tg C per year, of which Indonesia releases 53.9±12.4 Tg C per year. Malaysian rivers emit 6.2±1.6 Tg C per year. These moderate values show that Southeast Asia is not the river outgassing hotspot as would be expected from the carbon-enriched peat soils. This is due to the relatively short residence time of dissolved organic carbon (DOC) in the river, as the peatlands, being the primary source of DOC, are located near the coast. Limitation of bacterial production, due to low pH, oxygen depletion or the refractory nature of DOC, potentially also contributes to moderate CO2 fluxes as this decelerates decomposition.
Tropical peatlands play an important role in the global carbon cycle due to their immense carbon storage capacity. However, pristine peat swamp forests are vanishing due to deforestation and peatland degradation, especially in Southeast Asia. CO2 emissions associated with this land use change might not only come from the peat soil directly but also from peat-draining rivers. So far, though, this has been mere speculation, since there has been no data from undisturbed reference sites. We present the first combined assessment of lateral organic carbon fluxes and CO2 outgassing from an undisturbed tropical peat-draining river. Two sampling campaigns were undertaken on the Maludam River in Sarawak, Malaysia. The river catchment is covered by protected peat swamp forest, offering a unique opportunity to study a peat-draining river in its natural state, without any influence from tributaries with different characteristics. The two campaigns yielded consistent results. Dissolved organic carbon (DOC) concentrations ranged between 3222 and 6218 μmol L−1 and accounted for more than 99 % of the total organic carbon (TOC). Radiocarbon dating revealed that the riverine DOC was of recent origin, suggesting that it derives from the top soil layers and surface runoff. We observed strong oxygen depletion, implying high rates of organic matter decomposition and consequently CO2 production. The measured median pCO2 was 7795 and 8400 μatm during the first and second campaign, respectively. Overall, we found that only 32 ± 19 % of the carbon was exported by CO2 evasion, while the rest was exported by discharge. CO2 outgassing seemed to be moderated by the short water residence time. Since most Southeast Asian peatlands are located at the coast, this is probably an important limiting factor for CO2 outgassing from most of its peat-draining rivers.
South-East Asia is home to one of the world's largest stores of tropical peatland and accounts for roughly 10 % of the global land-to-sea dissolved organic carbon (DOC) flux. We present the first ever seasonally resolved measurements of DOC concentration and chromophoric dissolved organic matter (CDOM) spectra for six peatland-draining rivers and coastal waters in Sarawak, north-western Borneo. The rivers differed substantially in DOC concentration, ranging from 120–250 µmol L−1 (Rajang River) to 3100–4400 µmol L−1 (Maludam River). All rivers carried high CDOM concentrations, with a350 in the four blackwater rivers between 70 and 210 m−1 and 4 and 12 m−1 in the other two rivers. DOC and CDOM showed conservative mixing with seawater except in the largest river (the Rajang), where DOC concentrations in the estuary were elevated, most likely due to inputs from the extensive peatlands within the Rajang Delta. Seasonal variation was moderate and inconsistent between rivers. However, during the rainier north-east monsoon, all marine stations in the western part of our study area had higher DOC concentrations and lower CDOM spectral slopes, indicating a greater proportion of terrigenous DOM in coastal waters. Photodegradation experiments revealed that riverine DOC and CDOM in Sarawak are photolabile: up to 25 % of riverine DOC was lost within 5 days of exposure to natural sunlight, and the spectral slopes of photo-bleached CDOM resembled those of our marine samples. We conclude that coastal waters of Sarawak receive large inputs of terrigenous DOC that is only minimally altered during estuarine transport and that any biogeochemical processing must therefore occur mostly at sea. It is likely that photodegradation plays an important role in the degradation of terrigenous DOC in these waters.
Nitrous oxide (N2O) and methane (CH4) are atmospheric trace gases which play important roles in the climate and atmospheric chemistry of the Earth. However, little is known about their emissions from rivers and estuaries, which seem to contribute significantly to the atmospheric budget of both gases. To this end concentrations of N2O and CH4 were measured in the Rajang, Maludam, Sebuyau and Simunjan rivers draining peatland in northwestern (NW) Borneo during two campaigns in March and September 2017. The Rajang River was additionally sampled in August 2016 and the Samunsam and Sematan rivers were additionally sampled in March 2017. The Maludam, Sebuyau, and Simunjan rivers are typical “blackwater” rivers with very low pH (3.7–7.8), very high dissolved organic carbon (DOC) concentrations (235–4387 mmol L−1) and very low O2 concentrations (31–246 µmol L−1; i.e. 13 %–116 % O2 saturation). The spatial and temporal variability of N2O and CH4 concentrations (saturations) in the six rivers or estuaries was large and ranged from 2.0 nmol L−1 (28 %) to 41.4 nmol L−1 (570 %) and from 2.5 nmol L−1 (106 %) to 1372 nmol L−1 (57 459 %), respectively. We found no overall trends of N2O with O2 or , or , and there were no trends of CH4 with O2 or dissolved nutrients or DOC. N2O concentrations showed a positive linear correlation with rainfall. We conclude, therefore, that rainfall is the main factor determining the riverine N2O concentrations since N2O production or consumption in the blackwater rivers themselves seems to be low because of the low pH. CH4 concentrations were highest at salinity = 0 and most probably result from methanogenesis as part of the decomposition of organic matter under anoxic conditions. CH4 in the concentrations in the blackwater rivers showed an inverse relationship with rainfall. We suggest that CH4 oxidation in combination with an enhanced river flow after the rainfall events might be responsible for the decrease in the CH4 concentrations. The rivers and estuaries studied here were an overall net source of N2O and CH4 to the atmosphere. The total annual N2O and CH4 emissions were 1.09 Gg N2O yr−1 (0.7 Gg N yr−1) and 23.8 Gg CH4 yr−1, respectively. This represents about 0.3 %–0.7 % of the global annual riverine and estuarine N2O emissions and about 0.1 %–1 % of the global riverine and estuarine CH4 emissions. Therefore, we conclude that rivers and estuaries in NW Borneo – despite the fact their water area covers only 0.05 % of the global river/estuarine area – contribute significantly to global riverine and estuarine emissions of N2O and CH4.