Effect of land-use changes on nitrous oxide (N2O) emission from tropical peatlands
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Transcript of Effect of land-use changes on nitrous oxide (N2O) emission from tropical peatlands
E�ect of land-use changes on nitrous oxide (N2O) emissionfrom tropical peatlands
Abdul Hadi a, K. Inubushi a,*, E. Purnomo b, F. Razie b, K. Yamakawa a,H. Tsuruta c
a Faculty of Horticulture, Chiba University, Matsudo, Chiba 271-8510, Japanb Faculty of Agriculture, Lambung Mangkurat University, Banjarbaru 70714, Indonesia
c National Institute of Agro-Environmental Sciences, Kan-nondai, Tsukuba 305-8604, Japan
Received 15 June 1999; accepted 30 March 2000
Importance of this paper: The e�ect of land-use changes on nitrous oxide (N2O) emission from tropical peatlands in
Indonesia and Malaysia was studied in the ®eld and in the laboratory. The amount of N2O emitted from the peatland varied
widely according to the land-use management, water contents, addition of fertilizer or organic waste and location of the site.
Changing natural peatland to cultivated land can have a signi®cant impact of either increasing or decreasing N2O emission
to the atmosphere depending on the land-use management and environmental conditions.
Abstract
Tropical peatlands could be a potential source of nitrous oxide (N2O) which has a signi®cant impact on global
warming. To reduce N2O emission and develop best management practices for peatlands, the formation and emission
rates of N2O as a�ected by land-use management (i.e., changing peatland into agricultural land) and the factors af-
fecting the process must be understood. Therefore, one ®eld and three laboratory incubation experiments were carried
out during 1998±99 using peatland soils from 12 sites in South Kalimantan (Indonesia) and one site in Sarawak
(Malaysia) to quantify the N2O emission and the factors a�ecting it. The results from the ®eld experiment showed that
land-use managements, changing water table and locations had a signi®cant impact on N2O emission. Changing
peatland into cultivated lands (cultivated upland and paddy ®eld) enhanced the N2O emission. For example, cultivated
upland Cassava crop resulted in the highest amounts of N2O emission (1.04 mg N mÿ2 hÿ1) compared to other
treatments. The N2O emission during 1998 was higher than those during 1999 because of the changing water table and
dry season in 1998. The laboratory experiments showed that the N2O emission was also strongly in¯uenced by land-use
management, soil moisture contents, addition of ammonium fertilizer or rice straw and soil depths. For example, the
¯ooded conditions stimulated the N2O emission compared to that at 60% moisture contents. Similarly, the addition of
ammonium fertilizer suppressed the N2O emission compared to control treatments because of the high ammonium
contents that inhibit nitri®cation. Nevertheless, incorporation of rice straw to soil samples from 20 to 40 cm soil depth
stimulated N2O emission. Ó 2000 Elsevier Science Ltd. All rights reserved.
Keywords: Denitri®cation; Land-use change; Nitri®cation; Nitrous oxide; Peat soil; Tropical peatlands
1. Introduction
Peatlands include soils which contain 30% or more
organic matter in the top 40 cm and cover 80% of the
area (FAO, 1988). Approximately 29 million ha is
Chemosphere ± Global Change Science 2 (2000) 347±358
* Corresponding author. Fax: +81-47-308-8720.
E-mail address: [email protected] (K. Inu-
bushi).
1465-9972/00/$ - see front matter Ó 2000 Elsevier Science Ltd. All rights reserved.
PII: S 1 4 6 5 - 9 9 7 2 ( 0 0 ) 0 0 0 3 0 - 1
tropical peatland worldwide (Takai, 1997). A large
portion of this tropical peatland exists in the Borneo
Island (Driesen, 1981; Takai, 1997), which belongs to
three countries (i.e., Indonesia, Malaysia and Brunei).
Recently, large areas of peatland have been con-
verted by constructing drainage ditches into agricultural
and aquacultural lands in South Kalimantan (Indone-
sia) and in Sarawak (Malaysia) because of the intensi-
®cation of agriculture due to growing population in
those areas (Moehansyah, 1988; MacKinnon et al.,
1996). For example, oil palm and rice crop have been
grown on most peatland in Sarawak (nearly 1 million
ha) and South Kalimantan (about 200,000 ha), respec-
tively (Ismunadji and Soepardi, 1984; Ahmad et al.,
1986; Radjagukguk, 1990).
Both natural and converted peat soils may act as a
potential source of N2O of which the global emission
rate approximately 15 Tg N yÿ1 (Bouwman, 1990).
Large amounts of ammonium �NH�4 � and nitrate �NOÿ3 �accumulate when organic matter in peat soil undergoes
either aerobic or anaerobic decomposition (Driesen,
1981; Ismunadji and Soepardi, 1984). This could pose a
great threat to the environment by emitting various
gases like nitrous oxide (N2O), methane (CH4) and
carbon dioxide (CO2). However, there is a lack of
quantitative information regarding the emission of N2O
from natural and converted peatland (Terry et al.,
1981a,b; Agustin et al., 1998). Therefore, the present
study was designed to investigate the formation and
emission of N2O from natural and converted tropical
peatlands and the factors a�ecting the process of N2O
emission.
2. Materials and methods
Four experiments (i.e., one ®eld experiment and three
laboratory incubation experiments) were carried out to
determine the impact of land-use management (i.e.,
converting natural peatland into agricultural land) and
Fig. 1. Map of the sampling sites.
348 A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358
Tab
le1
Sit
elo
cati
on
,d
escr
ipti
on
an
dp
hysi
coch
emic
al
pro
per
ties
of
the
soil
su
sed
Lo
cati
on
Sit
eco
de
GP
SL
an
du
sem
an
agem
ent
Pea
tth
ick
nes
s
(cm
)
Sam
ple
dep
th
(cm
)
pH
(1:5
)T
ota
lo
rg-C
(gk
gÿ1
)
To
tal
N
(gk
gÿ1
)
CE
C
(cm
ol
(+)
kgÿ1
)
Ga
mb
ut
G-1
3°2
50 S
Un
cult
iva
ted
up
lan
d®
eld
70±100
0±10
3.8
612.5
15.0
75.8
11
4°4
00 E
10±20
3.4
620.2
12.8
92.0
20±30
3.2
615.6
8.9
103.2
G-2
3°2
50 S
Un
cult
iva
ted
up
lan
d®
eld
10±40
0±10
3.8
485.5
9.6
132.8
11
4°4
00 E
10±20
3.6
306.0
4.8
70.6
20±30
3.8
338.3
5.9
72.7
G-3
3°2
50 S
Sec
on
da
ryfo
rest
100±200
0±10
3.2
485.7
15.9
103.4
11
4°4
00 E
10±20
3.0
368.3
10.1
71.0
20±30
3.3
506.3
9.7
108.1
Jel
ap
at
J-4
Pa
dd
y®
eld
(1yea
rru
nn
ing)
5±20
0±10
3.3
192.2
10.8
40.5
10±20
3.6
47.1
4.1
40.8
20±30
3.2
0.0
1.6
30.3
J-5
Sec
on
da
ryfo
rest
15±25
0±10
3.4
240.6
11.8
62.4
10±20
3.2
73.3
3.6
30.1
20±30
3.3
79.4
2.1
34.6
Ba
ram
ba
iB
-63°0
00 S
Pa
dd
y®
eld
(3yea
rsru
nn
ing)
40±50
0±10
3.3
123.7
5.1
49.2
11
4°4
20 E
10±20
3.2
235.2
7.1
68.9
20±30
3.6
246.9
7.0
52.3
B-7
3°0
00 S
Cu
ltiv
ate
du
pla
nd
®el
d(c
ass
ava
cro
p,
3y
ears
run
nin
g)
70
0±10
3.4
140.8
5.7
43.2
11
4°4
20 E
10±20
3.4
146.6
3.9
44.6
20±30
3.2
142.9
5.3
44.7
B-8
2°5
90 S
Sec
on
da
ryfo
rest
5±15
0±10
3.6
139.7
5.4
56.6
11
4°4
30 E
10±20
3.4
27.5
4.1
32.2
20±30
3.5
50.4
4.3
41.3
Ma
rgasa
riM
-92°5
60 S
Sec
on
da
ryfo
rest
20±60
0±10
4.3
237.6
9.2
61.6
11
5°0
10 E
10±20
4.6
163.2
9.1
54.3
20±30
4.7
140.4
3.9
25.6
Am
un
tai
A-1
02°2
60 S
Ric
e±so
yb
ean
rota
tio
n®
eld
(6yea
rs
run
nin
g)
20±40
0±15
a4.6
574.3
13.2
103.7
11
5°2
30 E
A-1
12°1
90 S
Pa
dd
y®
eld
(2yea
rsru
nn
ing)
100±200
0±10
4.7
458.6
15.0
38.0
11
5°2
10 E
10±20
4.3
507.1
15.3
26.1
20±30
4.1
556.4
15.6
29.3
A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358 349
other environmental factors on the emission of N2O
during 1998±99, using peatland soils from 12 sites in
South Kalimantan (Indonesia) and one site in Sarawak
(Malaysia) (Fig. 1). The details of each experiment is
given below.
2.1. Field experiment: emission of N2O from natural and
converted tropical peatlands
This study was conducted in December 1998 and
December 1999, using 11 natural and converted peat-
land sites in South Kalimantan. Out of one million ha
peatland area, 500,000 ha were surveyed and then 11
sites were selected for this study. The 11 peatland sites
comprised of ®ve secondary forests, three converted
paddy ®elds, one converted upland ®eld grown with
cassava and two converted uncultivated uplands. Sites in
Barambai and Jelapat are in¯uenced by daily tidal
movement. The sites codes, position and chemical
properties are given in Table 1. The soil depths varied
and ranged from 10 to 200 cm. In most sites, peat soils
were derived from a mixture of wood and grass, except
G-1, G-2 and G-3 in Gambut where peat soils were
derived from grass only (Sabiham, 1988, 1989).
Nitrous oxide (N2O) was measured by inserting a gas
chamber made up of PVC pipe (21 cm diameter and 14
cm long). The gas chamber was closed from the upper
end, having a septum port in the center, which was at-
tached to a rubber tube. Gas samples were collected by
inserting a 35 ml syringe into the tube and then sucking
the air. Four gas samples were collected from each
chamber at time 0, 5, 10 and 15 min after the enclosure.
Gas samples were then transferred into a vacuum vial
(22 ml) and analyzed for N2O using a Shimadzu GC-7A
gas chromatograph with 63Ni electron-capture detector.
Nitrous oxide (N2O) was separated on a Porapak Q
column (0.002 ´ 2 m) by keeping oven and detector
temperatures at 40°C and 350°C, respectively. The N2O
had a retention time of 2.9 min at a ¯ow rate of 20 ml
minÿ1 of CH4 and Ar gas mixture (volume ratio 5:95).
The emission rate of N2O was calculated from the in-
crease in N2O concentration in the chamber head space
per unit time multiplied by the height of the gas
chamber.
Redox potential (Eh) in the ®eld was measured by
inserting a platinum electrode in three soil depths (i.e.,
10, 20 and 30 cm) as described by Hesse (1971). Ground
water table was measured by inserting a pizometer into
the soil. Water samples from soil-pore were collected by
inserting a porous cup (Daiki Physicochemical Compa-
ny, Japan) and sucking water into a 50 ml syringe.
Water samples were analyzed for Fe2� concentration
using Merck RQ ¯ex plus (Merck, Germany; Maruo
et al., 1998).
Soil samples were taken during 1998 and 1999 from
three soil depths (0±10, 10±20 and 20±30 cm) andTab
le1
(Co
nti
nu
ed)
Lo
cati
on
Sit
eco
de
GP
SL
an
du
sem
an
agem
ent
Pea
tth
ick
nes
s
(cm
)
Sam
ple
dep
th
(cm
)
pH
(1:5
)T
ota
lo
rg-C
(gk
gÿ1
)
To
tal
N
(gk
gÿ1
)
CE
C
(cm
ol
(+)
kgÿ1
)
A-1
22°1
80 S
Sec
on
da
ryfo
rest
>200
0±10
4.1
471.9
20.8
37.6
11
5°2
10 E
10±20
4.9
410.5
13.7
65.8
20±30
4.3
513.6
19.0
53.0
Sara
wa
kS
2°4
90 N
Oil
pa
lmp
lan
tati
on
100±200
0±10
4.4
11
1°5
40 E
10±20
4.0
715.8
15.9
20±40
4.1
917.4
16.2
40±60
3.4
835.7
11.2
60±80
4.0
946.9
7.7
aO
nly
on
eso
ild
epth
(i.e
.,0
±1
5cm
)w
as
tak
enfr
om
site
A-1
0,
on
Feb
ruary
1998.
350 A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358
analyzed for NH�4 and NOÿ3 by using the methods de-
scribed by Anderson and Ingram (1989) and Hayashi et al.
(1997), respectively. A composite soil sample from each
site and soil depth was taken in 1999, air dried, sieved
<2 mm and analyzed for various soil chemical properties
(i.e., pH, organic carbon and total N) (Table 1).
2.2. Laboratory incubation experiment 1: e�ect of
ammonium fertilizer on N2O emission
A laboratory incubation was carried out to investi-
gate the in¯uence of ammonium fertilizer (NH4)2SO4 on
N2O emission. During 1998, soil samples were collected
from three soil depths (0±10, 10±20 and 20±30 cm) of the
converted paddy ®eld site B-6. Five grams soil on oven
dry basis was amended with (NH4)2SO4 at the rate of
100 kg N haÿ1. The soil samples were then transferred
into 60 ml serum bottles and incubated at 28°C for 14
days. The controls (soil only) were treated in similar
way. The emission of N2O was carried out on daily basis
for the ®rst 6 days and then on day 14. All analyses were
carried out in triplicate.
In another set of soil sample, three control soil
samples were extracted on day 0 and analyzed for NH�4and NOÿ3 as described earlier. Then additional soil
samples (three amended with (NH4)2SO4 and three
controls) were incubated under similar conditions and
analyzed for NH�4 and NOÿ3 contents after 7 days.
2.3. Laboratory incubation experiment 2: e�ect of mois-
ture contents and land-use management on N2O emission
A laboratory incubation was carried out to determine
the e�ect of soil water contents on the emission of N2O
from tropical peatlands. Soil samples were collected
from rice±soybean rotation ®eld (six years running
A-10), paddy ®eld (two years running A-11) and forest
(A-12) and had a moisture content of 31%, 63% and
71%, respectively, because of the drought weather in
1997 and early 1998. To measure the emission of N2O at
60% H2O level, deionized H2O was added to soils from
rice±soybean rotation ®eld; while those samples of
paddy ®eld and forest were dried to bring them to 60%
moisture level. Soil samples were transferred into 120 ml
serum bottles and incubated at 28°C for 100 days. An-
other set of soil samples were prepared similarly and
incubated under ¯ooded condition (i.e., 2 cm water
depth) by adding deionized water. N2O emission was
carried out at 2, 5, 13, 46, 60 and 100 days of incubation.
The NH�4 and NOÿ3 concentrations were measured at
day 0, 5, 60 and 100 days of incubation.
To determine the optimum moisture level for opti-
mum N2O emission, soil samples from paddy ®eld site
A-11 were ®rst brought to 70%, 80% and 100% moisture
levels and submerged condition, and were then taken
into 120 ml serum bottles. These soil samples were in-
cubated at 28°C for 2 days and analyzed for N2O
emission.
2.4. Laboratory incubation experiment 3: e�ect of rice
straw and ammonium fertilizer on N2O emission
A laboratory incubation was conducted to determine
the e�ect of rice straw and ammonium fertilizer on
emission of N2O from soil samples taken from di�erent
depths. Soil samples were collected from ®ve soil depths
(0±10, 10±20, 20±40, 40±60 and 60±80 cm) in Sarawak
(Malaysia). Ten grams moist soils were placed in 60 ml
Table 2
Emission of N2O from di�erent land-use management in South Kalimantan (Indonesia)
Site code Land-use management N2O emission (mg N mÿ2 hÿ1)
1998 1999
Average values SD Average values SD
G-1 Uncultivated upland 0.12 0.01 )0.03 0.01
G-2 Uncultivated upland 0.01 0.18 0.02 0.01
G-3 Secondary forest 0.04 0.02
J-4 Paddy ®eld (1 year running) 0.03 0.05
J-5 Secondary forest 0.02 0.04
B-6 Paddy ®eld (3 years running) 0.08 0.06 0.04 0.03
B-7 Cultivated upland ®eld (cassava
crop 3 years running)
1.04 0.10 0.16 0.07
B-8 Secondary forest 0.10 0.08
M-9 Secondary forest )0.02 0.02
A-11 Paddy ®eld (2 years running) 0.14 0.13
A-12 Secondary forest 0.03 0.01
A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358 351
Tab
le3
Gro
un
dw
ate
rle
vel
,E
hv
alu
es,
NH� 4
,N
Oÿ 3
an
dF
e2�
con
cen
trati
on
so
fp
eatl
an
din
So
uth
Kali
man
tan
du
rin
g1998±99
Sit
eco
de
La
nd
-use
ma
na
gem
ent
19
98
1999
Gro
un
d
wa
ter
(cm
)
NH� 4
(lg
Ngÿ1
soil
)
NOÿ 3
(lg
Ngÿ1
soil
)
Eh
(mV
)F
e2�
(mg
Lÿ1
)
Gro
un
d
wate
r(c
m)
NH� 4
(lg
Ngÿ1
soil
)
NOÿ 3
(lg
Ngÿ1
soil
)
Eh
(mV
)F
e2�
(mg
Lÿ1
)
G-1
Un
cult
ivate
du
pla
nd
10
34
.4a
11.0
352
3.4
15.1
788.3
31.3
358
<0.5
14
.5b
15.7
214
0.7
1150.1
20.7
7<
0.5
8.7
c10.9
102
2.2
633.8
18.8
157
<0.5
G-2
Un
cult
ivate
du
pla
nd
)4
4.1
8.5
124
14.7
)2.1
396.6
46.6
124
1.3
1.9
2.5
)310
8.2
219.8
10.5
)10
1.0
)168
14.6
121.3
11.9
)81
1.2
G-3
Sec
on
da
ryfo
rest
10
571.3
24.9
323
0.5
637.0
24.0
60
<0.5
1361.9
29.0
185
<0.5
J-4
Pa
dd
y®
eld
(1y
ear
run
nin
g)
)5.1
281.6
57.6
)30
97.0
5.8
)90
43.8
6.4
55
J-5
Sec
on
da
ryfo
rest
)6.4
182.9
19.2
)72
40.4
11.6
29
45.2
9.6
)15
B-6
Pa
dd
y®
eld
(3y
ear
run
nin
g)
08
3.5
1.7
56
200
)5.8
367.6
20.6
)88
<0.5
87
.93.3
130
135
347.6
26.1
)120
<0.5
58
.74.4
22
43
269.1
52.8
)156
<0.5
B-7
Cu
ltiv
ate
du
pla
nd
®el
d
(ca
ssa
va
cro
p3
yea
rs
run
nin
g)
25
15.0
164.8
15.9
)130
1.6
142.2
9.6
)6
125
312.8
17.1
)47
98
B-8
Sec
on
da
ryfo
rest
25.5
141.6
10.9
36
<0.5
66.2
18.2
)133
10.5
44.9
4.0
55
24
M-9
Sec
on
da
ryfo
rest
)3.7
612.0
15.2
)171
0.7
158.3
19.1
)155
<0.5
68.8
3.3
)174
2.1
A-1
1P
ad
dy
®el
d(2
yea
rs
run
nin
g)
)2.7
328.9
17.1
15
1.0
512.2
41.3
96
1.1
69.1
23.7
80
1.0
A-1
2S
eco
nd
ary
fore
st0
520.6
50.2
43
854.0
83.9
48
<0.5
751.1
72.2
22
<0.5
aS
oil
dep
th0
±1
0cm
.b
So
ild
epth
10
±20
cm.
cS
oil
dep
th2
0±
30
cm.
352 A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358
serum bottles. Soil samples were then amended with
recommended doses of rice straw powder (4 ton haÿ1) or
ammonium sulfate (100 kg N haÿ1). The head space was
replaced with air and evacuated several times. The serum
bottles were sealed by using butyl rubber stopper and an
aluminum crimp and incubated at 28°C for 28 days.
Nitrous oxide emission was carried out on weekly basis
and quanti®ed as described earlier.
At the end of incubation, soils treated with rice straw
were analyzed for water-soluble organic carbon, using
Total Organic Carbon analyzer 5000 (Shimadzu, Japan),
ammonium and nitrate concentrations.
3. Results and discussion
3.1. Characteristics of peatlands
Most of the peat soils considered in this study are
classi®ed as shallow peat soils because the peat depths
were <100 cm except in sites G-3, A-11, A-12 and S,
where the peat depth ranged from 100 to 200 cm or more
(medium to deep) (Radjagukguk, 1990). The peat soils
were strongly acidic having a pH value less than 5. The
organic carbon contents varied with locations and soil
depths and ranged from 0 to 947 g C kgÿ1 soil. The total
nitrogen also showed variation with locations and soil
depths and were in the ranged of 2±21 g N kgÿ1 soil
(Table 1).
3.2. Field experiment: emission of N2O from natural and
converted tropical peatlands
The emission of N2O was signi®cantly a�ected by
land-use management (Table 2). During 1998, the N2O
emission was the highest (i.e., 1.04 mg N2O-N mÿ2 hÿ1)
in the cultivated upland peat soils (site B-7) followed by
uncultivated upland (site G-1) and then paddy ®eld (site
B-6); while uncultivated upland (site G-2) resulted in the
lowest N2O emission (0.01).
The N2O emission during 1999 followed similar
pattern and exhibited variations with di�erent land-use
management, but the N2O emission rates were lower
than those observed during 1998 (Table 2). The N2O
emission was the highest (i.e., 0.16 mg N2O-N mÿ2 hÿ1)
in cultivated upland peat soils (site B-7) followed by
paddy ®eld (site A-11) and secondary forest (site B-8).
The N2O emission in other sites were lower and were in
this order: paddy ®eld (B-6) and secondary forest (site
G-3) > paddy ®eld (site J-4) and secondary forest (site A-
12) > secondary forest (site J-5) and uncultivated upland
(site G-2). The uncultivated upland (site G-1) and sec-
ondary forest (site M-9) resulted )0.03 and )0.02 mg
N2O-N mÿ2 hÿ1, respectively. The di�erence in N2O
emission from di�erent sites was probably due to the
di�erent land-use managements, environmental condi-
tions (i.e., groundwater table) and other soil chemical
properties (which will be discussed later).
The groundwater levels measured during 1998 and
1999 were a�ected by land-use management (Table 3).
During 1998, groundwater was generally low except at
site G-2 which was ¯ooded. Low groundwater in 1998
was caused by the unusual long drought season in 1997
and 1998. Contrary to that, during 1999, most of the
experimental sites were water ¯ooded except G-1, G-3,
B-7 and B-8.
The variations in N2O emission could also be due to
the changing groundwater levels. The highest amount of
N2O emission from site B-7 compared to the lowest N2O
emission at site G-2 clearly indicates that the N2O
emission was maximum at non-¯ooded conditions. The
¯uctuation of groundwater due to the tidal movement in
site B-7 may also have contributed to the high N2O
emission in this site. These results have some practical
implication in the management of N2O emission from
peatland; the emission will be more at sites where the
water table ¯uctuated. In contrast, the ¯ooded condi-
tions at site G-2 was not favorable for the nitri®cation,
resulting in the lowest N2O emission. The presence of
supernatant water at ¯ooded sites might have also
Table 4
E�ect of ammonium fertilizer on emission of N2O, soil pH, NH�4 and NOÿ3 concentrations in paddy ®eld soil (site B-6) in South
Kalimantan
Sample
depth
(cm)
Treatments N2O emission (ng N2O-N gÿ1 dry soil) pH NH�4(lg N gÿ1 soil)
NOÿ3(lg N gÿ1 soil)
Day 1 Day 2 Day 3 Day 4 Day 6 Day 14 Day 0 Day 14 Day 0 Day 7 Day 0 Day 7
0±10 Control
(NH4)2SO4
0.00 6.07 9.17 13.48 25.19 25.05 3.40 3.40 83.5 105.1 1.7 3.09
3.90 2.41 0.00 0.00 0.00 0.00 3.36 1111.3 145.3 19.15
10±20 Control
(NH4)2SO4
5.48 8.30 9.80 5.45 0.00 0.00 3.49 3.70 87.9 119.7 3.3 2.71
5.44 3.54 0.00 0.00 0.00 0.00 3.45 1115.9 151.9 15.91
20±30 Control
(NH4)2SO4
0.00 3.90 6.29 6.90 11.15 8.43 3.49 3.40 28.7 73.2 4.4 4.35
0.00 0.00 0.00 0.00 0.00 0.00 3.41 1086.9 197.4 14.90
A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358 353
Tab
le5
E�
ect
of
mo
istu
reco
nte
nt
an
dla
nd
-use
ma
na
gem
ent
on
the
emis
sio
ns
of
N2O
,N
H� 4
an
dN
Oÿ 3
con
cen
trati
on
sin
top
ical
pea
tlan
dso
ilsa
Da
ys
Tre
atm
ent
N2O
(ng
Ngÿ1
soil
hÿ1
)N
H� 4
(ug
gÿ1
soil
)N
Oÿ 3
(ug
gÿ1
soil
)
Sit
ebA
-10
A-1
1A
-12
A-1
0A
-11
A-1
2A
-10
A-1
1A
-12
0C
on
tro
l157.0
143.0
190.0
0.5
20.0
32.8
2C
on
tro
l2
.4(1
.7)
1.9
(1.2
)0.2
(0.0
1)
Flo
od
ed6
.7(2
.0)
347.4
(18.8
0)
163.0
(13.1
)
5C
on
tro
l0
.4(0
.03
)0
.3(0
.05)
0.4
(0.1
)147.0
39.0
19.0
16.1
7.2
23.3
Flo
od
ed0
.2(0
.1)
1.0
(0.3
)0.2
(0.0
2)
8.3
152.0
189.7
05.3
10.0
13
Co
ntr
ol
0.1
(0.0
7)
0.0
7(0
.05)
0.1
(0.0
3)
Flo
od
ed0
.02
(0.0
3)
0.0
0(0
.00)
0.0
0(0
.00)
46
Co
ntr
ol
0.3
(0.0
2)
0.3
(0.0
2)
0.1
(0.0
2)
Flo
od
ed0
.4(0
.02
)0
.1(0
.03)
0.1
(0.0
1)
60
Co
ntr
ol
77.5
9.4
14.1
2.5
42.2
38.0
Flo
od
ed25.6
59.4
201.0
017.2
22.0
10
0C
on
tro
l0
.2(0
.02
)0.7
3(0
.61)
0.2
(0.0
4)
8.1
7.0
7.6
5.0
15.2
19.0
Flo
od
ed0
.6(0
.60
)1
6.4
1(1
.27)
22.1
(14.5
)14.0
21.2
218.0
40.2
38.0
44.0
aN
um
ber
sin
pa
ren
thes
isin
dic
ate
sta
nd
ard
dev
iati
on
of
trip
lica
tes
mea
sure
men
ts.
bA
-10
:ri
ce±
soy
bea
nro
tati
on
®le
d,
A-1
1:
pa
dd
y®
eld
,A
-12
:se
con
dary
fore
st.
354 A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358
provided less di�usivity of soil in emitting N2O from
¯ooded sites (Terry et al., 1981a; Keller and Reiners,
1994; Mosier and Delgado, 1997).
The di�erences in groundwater level may have also
resulted in the signi®cant di�erence in N2O emission
measured during 1998 and that measured during 1999.
The emission during 1998 was enhanced by the drier
®eld, hence resulted in higher N2O emission.
Soil ammonium concentration varied with di�erent
peatland sites and soil depths (Table 3). The soil NH�4concentration during 1998 ranged from 2 to 89 lg NH�4gÿ1 soil, while the soil NH�4 concentration during 1999
was signi®cantly higher than that of 1998 and ranged
from 40.4 to 1362 lg NH�4 gÿ1 soil. Soil nitrate con-
centration during 1998 and 1999 followed similar trend
of changing with sites and were in similar range (i.e.,
2±16 in 1998 and 3.3±83 in 1999) (Table 3).
Redox potentials (Eh) measured during 1998 and
1999, indicated that they changed with experimental
sites and were generally higher, where the groundwater
level was lower (Table 3). The Fe2� concentration in
pore water during 1998 was higher (i.e., 200 mg Fe2� Lÿ1
in site B-6), than that during 1999.
3.3. Laboratory incubation experiment 1: e�ect of
ammonium fertilizer on N2O emission
The addition of (NH4)2SO4 to soil signi®cantly re-
duced the emission of N2O compared to the control
treatments (Table 4). The N2O emission in the fertilizer
treated soils was very fast during the ®rst 2 days of in-
cubation and became slow for the remaining period of
incubation. The higher NH�4 and lower NOÿ3 concen-
trations measured on day 7 indicated that nitri®cation
was much slower which could have lowered the rate of
N2O emission from ammonium fertilizer treated soils.
This is supported by Heynes (1986) and Zaman et al.
(1999) who reported slower nitri®cation rate due to high
ammonium concentration and anaerobic condition.
Fig. 2. Emission rate of N2O at di�erent water content of soil
taken from paddy ®eld site B-6 in South Kalimantan. Bars in-
dicate standard error of two replicates.
Fig. 3. Changes in nitrous oxide concentrations in head space
of (A) unamended, (B) ammonium sulfate-amended and (C)
rice straw-amended peat soils from Sarawak. Data with coef-
®cient of variance more than 100% were excluded from these
graphs because the big variations may be due to experimental
errors.
A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358 355
3.4. Laboratory incubation experiment 2: e�ect of mois-
ture contents and land-use management on N2O emission
The N2O emission was strongly in¯uenced by soil
water contents and land-use managements (Table 5).
Incubating soil samples at ¯ooded condition, resulted in
signi®cantly higher amounts of N2O emission than those
at 60% water contents, indicating that the moisture
content of 60% limited the N2O formation. It can be
through retarding the proliferation of N2O producing
microorganism by an insu�ciency of water (Paul and
Clark, 1996). These results are contrary to our ®eld
measurements, where ¯ooded conditions resulted in
lower N2O emission. These could be due to the variable
®eld conditions plus some other variables which were
not considered in this study. On day 2 of the incubation
period, the paddy ®eld soils (A-11) resulted in signi®-
cantly higher amount of N2O (347.4 ng gÿ1 soil hÿ1)
than that from secondary forest soil (A-12) (162.6) at
¯ooded conditions; while the rice±soybean rotation ®eld
(A-10) resulted in the lowest N2O emission rate (6.4) at
the same moisture content. These variations are proba-
bly due to di�erence in land-use managements as dis-
cussed earlier in ®eld experiment. The N2O emission
during the remaining incubation period reduced except
on day 100, when secondary forest soils (A-12) resulted
in a high N2O emission followed by paddy ®eld (A-11) at
¯ooded conditions.
The NH�4 and NOÿ3 concentrations changed with
land-use management and soil water contents (Table 5).
The soil NH�4 concentration in paddy ®eld (A-11) and
secondary forest (A-12) did not decrease quickly when
the soils were incubated under ¯ooded conditions; while
those at 60% water contents disappeared at a faster rate.
This might be due to the fast nitri®cation at 60% water
content than that at ¯ooded condition because all nit-
ri®ers are strictly aerobes (McLaren and Cameron, 1996;
Paul and Clark, 1996). The NOÿ3 concentration de-
creased quickly during the ®rst 5 days of incubation and
increased afterward when the soils were incubated under
¯ooded condition indicating fast denitri®cation rates at
¯ooded conditions than at 60% moisture content. These
results con®rm previous studies that denitri®cation
proceeds at faster rate under ¯ooded conditions
(Bouwman, 1990; Paul and Clark, 1996).
The amount of N2O emitted from soil taken from
paddy ®eld site B-6 was signi®cantly a�ected by soil
water content (Fig. 2). The N2O emission rate was
highest from 100% water content followed by that from
¯ooded soil, 80% and 70% moisture contents in this
order. This indicates that 100% moisture content fa-
vored the N2O emission. Flooding the soil resulted in the
lower N2O emission than that incubated under 100%
moisture level for the same reason explained for the ®eld
experiment (Section 3.2).
3.5. Laboratory incubation experiment 3: e�ect of rice
straw, ammonium fertilizer and soil depths on N2O
emission
The emission of N2O during the 28 days of incu-
bation was strongly in¯uenced by soil samples from
di�erent depths and by the addition of rice straw and
(NH4)2SO4 (Fig. 3). During the ®rst 7 days, the
(NH4)2SO4 or rice straw amended soils suppressed the
N2O emission in soil samples from all ®ve depths ex-
cept (20±40 cm). This could have been due to the in-
hibitory e�ect of NH�4 on nitri®cation which provides
substrate (i.e., NOÿ3 ) for denitri®cation (Haynes, 1986;
Zaman et al., 1999). This is con®rmed when the sur-
face soil layer (0±10 cm) of the unamended soils re-
sulted in higher N2O than the same layers of amended
soils during the ®rst two weeks of incubation. In
amended soils, soil samples from (20±40 cm) produced
more N2O than other soil depths. The denitri®cation
Table 6
Changes in NH�4 and NOÿ3 concentrations and water soluble organic carbon (SOC) during 28 days after addition of rice straw to
tropical peatland soil from Sarawak (site S)
Soil depth (cm) Incubation time (day) NH�4 (ug N gÿ1 soil) NOÿ3 (ug N gÿ1 soil) SOC (mg C gÿ1 dry soil)
0±10 0 ± 2.2 6.4
28 ± 0.0 2.2
10±20 0 291.2 0.0 5.5
28 5.7 0.0 1.9
20±40 0 286.4 4.3 4.9
28 5.4 3.3 1.1
40±60 0 68.4 4.6 5.1
28 4.4 3.3 1.7
60±80 0 37.2 5.5 4.9
28 10.9 5.1 1.7
356 A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358
in soil depth 20±30 cm of rice straw-amended soil was
enhanced by the presence of high water-soluble carbon
(i.e., rice straw powder). The water-soluble carbon
coupled with wet conditions might have resulted in the
highest N2O emission from soil depth 20 to 40 cm of
rice straw-amended soil. The N2O emission from both
amended and unamended treatments in subsoil layers
(below 40 cm) were very low (less than 0.5 lg N gÿ1
soil). This could be due to the low availability of
carbonaceous materials (Table 6) and low microbial
activity (Inubushi et al., 1998).
4. Conclusions
The results from the ®eld experiment showed that
land-use managements, changing water table and loca-
tions had a signi®cant impact on N2O emission.
Changing peatland into cultivated lands (cultivated up-
land and paddy ®eld) enhanced the N2O emission. For
example, cultivated upland Cassava crop resulted in the
highest amounts of N2O emission (1.04 mg N mÿ2 hÿ1)
compared to other treatments. The N2O emission during
1998 was higher than those during 1999 because of the
changing water table and dry season in 1998. The lab-
oratory experiments showed that the N2O emission was
also strongly in¯uenced by land-use management, soil
moisture contents, addition of ammonium fertilizer or
rice straw and soil depths. For example, the ¯ooded
conditions stimulated the N2O emission compared to
that at 60% moisture contents. Similarly, the addition of
ammonium fertilizer suppressed the N2O emission
compared to control treatments because of the high
ammonium contents that inhibit nitri®cation. Never-
theless, incorporation of rice straw to soil samples from
20 to 40 cm soil depth stimulated N2O emission indi-
cative of favorable conditions for both nitri®cation and
denitri®cation.
Acknowledgements
We acknowledge H. Ari®n (professor of Soil Science
at Lambung Mangkurat University) for his valuable
comments, suggestions and help. The ®eld work in
South Kalimantan was possible by the help of Messrs.
Hairil Ifansyah, Sudirman and Tau®k Fadilah (sta� and
students of Lambung Mangkurat University) and Mu-
hammad Haridi (sta� of Agricultural Extension Station
in Amuntai). The help of Dr. Mohammad Zaman
(Lincoln University, New Zealand) during the prepara-
tion of this manuscript is highly acknowledged. This
work was partly supported by the Grant from the En-
vironmental Agency, Japan.
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Abdul Hadi is a sta� member of Lambung Mangkurat Uni-versity, Banjarmasin (Indonesia) and is now a Ph.D student atChiba University (Japan). His research interest is on the man-agement of wetlands. So far, he has published ®ve papers onthis topic.
358 A. Hadi et al. / Chemosphere: Global Change Science 2 (2000) 347±358