Chemosphere 52 (2003) 603–608 www.elsevier.com/locate/chemosphere Seasonal changes of CO2, CH4 and N2O fluxes in relation to land-use change in tropical peatlands located in coastal area of South Kalimantan K. Inubushi a,* , Y. Furukawa a, A. Hadi b, E. Purnomo b, H. Tsuruta c a Faculty of Horticulture, Chiba University, Matsudo, Chiba 271-8510, Japan Faculty of Agriculture, Lambung Mangkurat University, Banjarbaru 70714, Indonesia National Institute for Agro-Environmental Sciences, Kan-nodai, Tsukuba 305-8604, Japan b c Abstract Tropical peatland could be a source of greenhouse gases emission because it contains large amounts of soil carbon and nitrogen. However these emissions are strongly influenced by soil moisture conditions. Tropical climate is characterized typically by wet and dry seasons. Seasonal changes in the emission of carbon dioxide (CO2 ), methane (CH4 ) and nitrous oxide (N2 O) were investigated over a year at three sites (secondary forest, paddy field and upland field) in the tropical peatland in South Kalimantan, Indonesia. The amount of these gases emitted from the fields varied widely according to the seasonal pattern of precipitation, especially methane emission rates were positively correlated with precipitation. Converting from secondary forest peatland to paddy field tended to increase annual emissions of CO2 and CH4 to the atmosphere (from 1.2 to 1.5 kg CO2 -C m2 y1 and from 1.2 to 1.9 g CH4 -C m2 y1 ), while changing landuse from secondary forest to upland tended to decrease these gases emissions (from 1.2 to 1.0 kg CO2 -C m2 y1 and from 1.2 to 0.6 g CH4 -C m2 y1 ), but no clear trend was observed for N2 O which kept negative value as annual rates at three sites. Ó 2003 Elsevier Science Ltd. All rights reserved. Keywords: Carbon dioxide; Histosol; Land-cover change; Methane; Nitrous oxide; Peat 1. Introduction Peatlands are technically defined as all lands where 80% of the area is covered by peat soil; a soil containing at least 30% by weight of organic matter, in cumulative layer of 40 cm or more (FAO, 1988), and typical landcover in wetland. Although wetlands occupy only 4–6% of the landÕs surface in the world (about 530–570 million ha) (Aselmann and Crutzen, 1989), it contains about 20– 25% of terrestrial carbon and nitrogen (Batjes, 1996). About 29 million ha is in the tropical zone, and a large * Corresponding author. Fax: +81-47-308-8720. E-mail address: [email protected] (K. Inubushi). portion of this tropical peat soil exists in the Borneo Island (Driesen, 1978; Takai, 1997). Tropical peatland could be a source of greenhouse gases emission because it contains large amounts of soil carbon (70 Gt; Immirzi et al., 1992) and nitrogen (Ismunadji and Soepardi, 1984; Driesen, 1978). The organic matter in the peat soils is naturally decomposed slowly but continuously. Decomposition of organic matter is basically the degradation of complex organic compounds, converting them partly to the simpler forms. The decomposition causes the loss of mass (commonly stated as ground subsidence) and releases by-products leading to the formation of a more stable peat soil. The demands of peatland for agricultural and aquacultural uses have been increasing (Ahmad et al., 1986; Radjagukguk, 1990; Kyuma, 1992). The conversion of 0045-6535/03/$ - see front matter Ó 2003 Elsevier Science Ltd. All rights reserved. doi:10.1016/S0045-6535(03)00242-X 604 K. Inubushi et al. / Chemosphere 52 (2003) 603–608 peatland always starts with the construction of drainage ditches in order to reduce the excess water that is commonly associated with natural peatland. Both natural and converted tropical peat soil can potentially control the dynamics of carbon dioxide (CO2 ), methane (CH4 ) and nitrous oxide (N2 O) (Bouwman, 1990). However, there is no quantitative data on the emission of these three gases from tropical peat soils, except our preliminary reports (Hadi et al., 2000) for the three gases from same area, Hadi et al. (2001) for N2 O from same state but inland peat soil, and Kiese and Butterbach-Bahl (2002) for N2 O and CO2 from tropical wet forest but not in peat soil. Moreover, seasonal changes of these gas emissions in tropical peat soil are poorly understood. Since the tropical climate is characterized typically by wet and dry seasons, seasonal patterns of these emissions are important for better estimations of the emissions, which are strongly influenced by soil moisture conditions. The present study was undertaken to investigate seasonal changes in the emission of CO2 , CH4 and N2 O over a year in relation to land-use change of tropical peatland in South Kalimantan, Indonesia. 2. Materials and methods 2.1. Site description The monthly measurements took place at the peatland near Gambut in South Kalimantan, Indonesia (Table 1). Traditional peatland reclamation in these area started in 1935, but intensive reclamation with construction of canals has been going on to establish paddy and then upland fields since late 1970s. Vegetation before the intensive reclamation was covered mostly by Macaranga sp. tree (up to 20 m) with Acrostichum aureum ferns (1–2.3 m height) (Sabiham, 1988, 1989), which still remain partly as secondary forest. Three sites were chosen to represent different land-uses; G-3––secondary forest, G-2––paddy field, and G-1––upland field, although paddy or upland crops have no longer produced due to their low fertilities, so they were nearly abandoned fields. However general land use change in this area is from secondary forest to paddy, then upland/ paddy rotation in 2–5 years intervals. Each site was surveyed following 100 100 m separate grids, so totally Table 1 Site location, description and physicochemical properties of the soils used (November 1999) Site code Location and land-use management Peat thickness (cm) Ground watera (cm) Sample depth (cm) H2 O KCl G-1 Abandoned upland crops field 00 (3°250 43 S, 114° 00 0 40 26 E) 70–100 )15.1 0–10 10–20 20–30 3.8 3.4 3.2 G-2 Abandoned paddy field 00 (3°250 51 S, 114° 00 0 40 14 E) 10–40 +2.1 0–10 10–20 20–30 G-3 Secondary forest 00 (3°250 53 S, 00 0 114°41 11 E) 100–200 )10.0 Ash (%) Total organic C (g kg1 ) Total N (g kg1 ) G-1 35.6 48.6 46.4 486 306 338 9.6 4.8 5.9 778 474 578 G-2 8.2 2.4 3.3 613 620 616 15.0 12.8 8.9 G-3 7.8 3.9 2.9 486 368 506 15.9 10.1 9.7 a Eh (mV) EC (mS m1 ) CEC (cmol (+) kg1 ) 3.0 2.9 2.0 358 7 157 14.1 17.6 20.1 75.8 92.0 103.2 3.8 3.6 3.8 3.0 3.0 3.1 124 )10 )81 23.3 14.4 12.5 132.8 70.6 72.7 0–10 10–20 20–30 3.2 3.0 3.3 2.3 2.3 2.3 323 60 185 27.7 19.7 14.7 103.4 71.0 108.1 Soluble organic C (mg kg1 ) NHþ 4 (mg kg1 ) NO 3 (mg kg1 ) Fe2þ (mg kg1 ) 397 220 121 46.6 10.5 11.9 <12 <12 <12 1432 1456 507 788 1150 634 31.3 20.7 18.8 31.1 19.6 28.7 1167 1444 1093 571 637 1362 24.9 24.0 29.0 12.1 <12 <12 pH Negative values for ground water table mean that it was below the ground surface. K. Inubushi et al. / Chemosphere 52 (2003) 603–608 three grids were set up. Distance between G-1 and G-2 was about 450 m and these sites were about 1.4–1.7 km away from G-3. In all sites, the peat soils were derived from a mixture of wood and grass (Sabiham, 1988, 1989; Inubushi et al., 1998). The depth of the peat layers varied from 10 cm to about 2 m. 2.2. Chemical properties of soil samples Soil samples were taken in November 1999 from 3 depths (0–10, 10–20, 20–30 cm) and used for laboratory measurement. The samples were kept in cold room (4 °C) until the time of use. Soil pH was measured with glass electrode after 1 h shaking with distilled water or KCl solution using a 1:5 (soil:water or KCl) ratio. Soil EC (electrical conductivity), CEC, ash, total C and N contents were determined according to the standard method of soil analysis (Black et al., 1981). The concentrations of ammonium and nitrate-N were measured in 2 M KCl extract by using the nitroprusside (Anderson and Ingram, 1989) and hydrazine reduction (Hayashi et al., 1997) methods, while Fe2þ by Merck RQ Frex plus (Sigma, Germany) after acetate extraction (pH 2.8), respectively. The amount of soluble organic C was measured by TOC meter (Shimadzu, TOC 5000) after 1 h extraction with distilled water at 1:5 ratios. 2.3. Greenhouse gases emission from tropical peatland Seasonal field measurements were conducted at three sites (G-1, G-2 and G-3) from November 1999 to January 2001 almost monthly in order to find temporal pattern of the emission of greenhouse gases from tropical peatlands. Rates of CO2 , CH4 and N2 O emissions were measured by the closed cylindrical chamber method (inner dia. 21.0 cm; height 14.0 cm). Gas samples were 605 taken with gas-tight syringe from the triplicate chamber and the concentrations of CO2 , CH4 and N2 O were quantified with gas chromatograph (Shimadzu 7A, Japan) equipped with thermal detector, frame ionized detector, and electron capture detector, respectively. Redox potential (Eh ) was measured with platinum electrodes at 10, 20 and 30 cm depth in the field. Ground water table was measured by a pizometer inserted into the soil. 3. Results and discussion 3.1. Chemical properties of soil samples Soil samples showed low pH in both water and KCl extract and contained 30–62% carbon and 0.5–1.6% nitrogen (Table 1). These characteristics are typical in the peat soils (Driesen, 1978; Ismunadji and Soepardi, 1984; Batjes, 1996; Bozkurt et al., 2001). High total C contents especially in G-2 were possibly derived partly from charcoal after natural fire in the past and deep plowing during land preparation for rice cultivation. During these land-use changes, water soluble C was also accumulated, while total nitrogen contents were relatively low. Water table was high in abandoned paddy field (G-2), so that soil Eh was relatively low and NHþ 4 and Fe2þ contents more in G-2 compared to others. 3.2. Seasonal changes of CO2 , CH4 and N2 O emission from tropical peatlands These gases emitted from the fields varied widely over a year (Fig. 1). CO2 was in the range from 40 to 380 mg C m2 h1 and rather high in March–May and December. CH4 was in the range from 0 to 1 mg C m2 h1 and Fig. 1. Seasonal changes in CO2 , CH4 and N2 O flux from tropical peatland in South Kalimantan as influenced by land-use management. 606 K. Inubushi et al. / Chemosphere 52 (2003) 603–608 higher in February–April than the rest of year. These gases did not show significant negative flux. While N2 O was in the range from )0.04 to +0.03 mg N m2 h1 , significant negative flux for 8 flux measurements during February–June and January among 33 measurements were indicating N2 O consumption from the atmosphere by soil microorganisms. In order to examine controlling factor of these gases emission, monthly means of precipitations and air temperatures were calculated as averages between those in Balikpapan (01°160 S, 116°540 E, 3m asl) and Pontianak (00°090 S, 109°240 E, 3m asl) where are the nearest available locations (NOAA, 2001). Although monthly mean air temperature was almost constant at 26–27 °C precipitation showed clear seasonal pattern (Fig. 2). Highest precipitation was observed around March when CH4 emission at three locations reached their peaks. The CO2 emission had no tendency to the changes in precipitation. Seasonal pattern of N2 O was not clear due to high variability particularly in large among the locations as similar to CO2 pattern. According to the correlation between precipitation and gas emission, CH4 emission was positively correlated with precipitation (Fig. 3), while N2 O was slightly but significantly correlated negatively with precipitation when G-1 data were excluded (Fig. 4). Emission of greenhouse gases is likely influenced by precipitation directly and indirectly. Soil moisture is one of the most important controlling factors for biological reactions in soil, including heterotrophic microorgan- Fig. 3. Correlation between precipitation and methane flux in three sites in South Kalimantan (p < 0:01). Fig. 4. Correlation between precipitation and N2 O flux in sites G-2 and G-3 in South Kalimantan (p < 0:05). Fig. 2. Seasonal changes of precipitation and air temperature in South Kalimantan. isms and plant roots, which produce CO2 . Therefore precipitation generally enhances CO2 emission. In case of tropical peatlands, however, raining emerges flooded water on soil surface during wet season, not only in paddy fields but also other fields in these peatlands, so that the soil becomes anaerobic and no general trend in CO2 could not be observed, while methanogenic bacteria produce more CH4 . During dry season, the soil became aerobic and methanogenic activity becomes low. Laboratory experiments by Moore and Dalva (1997) using core samples taken from swamps and peat bogs in Canada show that CH4 emission exhibited a negative logarithmic correlation with the depth of the groundwater level whereas CO2 emission exhibited a positive linear correlation with this depth. Such discrepancy K. Inubushi et al. / Chemosphere 52 (2003) 603–608 607 Table 2 Effects of land use management on CO2 , CH4 and N2 O emission during 1 year. Numerical values are indicating the means of triplicates and standard deviations Site code Location and land-use management Total CO2 emission (g C m2 y1 ) Total CH4 emission (g C m2 y1 ) Total N2 O emission (mg N m2 y1 ) G-1 G-2 G-3 Abandoned upland crops field Abandoned paddy fields Secondary forest 990 110 1540 290 1200 430 0.6 0.7 1.9 0.5 1.2 0.4 )110 82 )37 80 )51 44 between these reports may be caused by the difference in the samplesÕ properties. In case of N2 O, precipitation enhances both aerobic nitrification and anaerobic denitrification trough enhanced microbial activities as shown in CO2 emission. However once floodwater comes up on the soil surface, highly soluble N2 O cannot be emitted easily to the atmosphere while further denitrified to N2 before emitted. Similar phenomenon has been observed in temperate paddy fields (Minami, 1997). Other factors such as available C should be examined in relation to the dynamics of these gases. 3.3. Effect of land-use change in tropical peatland on greenhouse gases Based on the seasonal changes of CO2 , CH4 and N2 O emissions from the peatlands, annual emission rate was calculated (Table 2). Although not significantly different due to large deviation, converting from secondary forest peatland to paddy field tended to increase annual emissions of CO2 and CH4 to the atmosphere (from 1.2 to 1.5 kg CO2 -C m2 y1 and from 1.2 to 1.9 g CH4 -C m2 y1 ), while changing land-use from secondary forest to upland tended to decrease these gases emissions (from 1.2 to 1.0 kg CO2 -C m2 y1 and from 1.2 to 0.6 g CH4 C m2 y1 ), but no clear trend was observed for N2 O which kept negative value as annual rates at three sites. We examined previous result about the effect of land-use from secondary forest to paddy field in South Kalimantan on CO2 , CH4 and N2 O emissions based on single measurement in November 1999 (Hadi et al., 2001), and fond similar changes in CO2 and CH4 , but not in N2 O which remained as positive higher values than this study. These findings confirmed our former results (Hadi et al., 2000) that the tropical peatland can be a source or a sink of N2 O; the land which was under oxic conditions acted as a source and that which was under reductive conditions acted as a sink. Controlling factors for N2 O emission is still not clear even in the seasonal pattern showed some trends. Converting natural peatland to cultivated land can either increase or decrease the emission of N2 O to the atmosphere depending on the soil moisture. However in case of CO2 and CH4 , estimation rates can be reasonably accurate based on the previous report. 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