e-issn: p-issn: organic and conservation systems … · indian institute of soil science nabibagh,...
TRANSCRIPT
~ 2362 ~
Journal of Pharmacognosy and Phytochemistry 2018; 7(2): 2362-2390
E-ISSN: 2278-4136
P-ISSN: 2349-8234
JPP 2018; 7(2): 2362-2390
Received: 01-01-2018
Accepted: 02-02-2018 RK Naresh
Department of Agronomy
Sardar Vallabhbhai Patel University of
Agriculture & Technology, Meerut, Uttar
Pradesh, India
Arvind Kumar
Rani Lakshmi Bai Central Agricultural
University, Jhansi- Uttar Pradesh, India
RK Gupta
Borlaug Institute for South Asia (BISA),
New Delhi, India
AK Shukla
Indian Institute of Soil Science Nabibagh,
Berasia Road, Bhopal, Madhya Pradesh,
India
SS Dhaliwal
Department of Soil Science; Punjab
Agricultural University, Ludhiana, Punjab,
India
RS Rathore
Uttar Pradesh Council of Agricultural
Research, (UPDASP), Lucknow- Uttar
Pradesh, India
Vivek
Department of Agronomy
Sardar Vallabhbhai Patel University of
Agriculture & Technology, Meerut, Uttar
Pradesh, India
Mukesh Kumar
Department of Horticulture, Sardar
Vallabhbhai Patel University of Agriculture
& Technology, Meerut, Uttar Pradesh, India
SP Singh
Department of Soil Science, Sardar
Vallabhbhai Patel University of Agriculture
& Technology, Meerut, Uttar Pradesh, India
Satyaveer Singh
Department of Agronomy,BAC, Sabour,
Bhagalpur, Bihar, India
SS Tomar
RVSKVV, ZARS-A, B. Road, Morena,
Madhya Pradesh, India
Hans Raj
K.V.K. Ghaziabad, Sardar Vallabhbhai
Patel University of Agriculture &
Technology, Meerut, Uttar Pradesh, India
SP Singh
K.V.K. Baghpat, Sardar Vallabhbhai Patel
University of Agriculture & Technology,
Meerut, Uttar Pradesh, India
RC Rathi
K.V.K. Beghra, Sardar Vallabhbhai Patel
University of Agriculture & Technology,
Meerut, Uttar Pradesh, India
NC Mahajan
Department of Agronomy
Sardar Vallabhbhai Patel University of
Agriculture & Technology, Meerut, Uttar
Pradesh, India
Rajendra Kumar
Department of Agronomy
Sardar Vallabhbhai Patel University of
Agriculture & Technology, Meerut, Uttar
Pradesh, India Correspondence
RK Naresh
Department of Agronomy
Sardar Vallabhbhai Patel University of
Agriculture & Technology, Meerut, Uttar
Pradesh, India
Organic and conservation systems enhanced
carbon sequestration potential and soil carbon
stock dynamics: A review
RK Naresh, Arvind Kumar, RK Gupta, AK Shukla, SS Dhaliwal, RS
Rathore, Vivek, Mukesh Kumar, SP Singh, Satyaveer Singh, SS Tomar,
Hans Raj, SP Singh, RC Rathi, NC Mahajan and Rajendra Kumar
Abstract
The study aims to elucidate the impact of organic inputs and conservation systems on soil carbon
sequestration and carbon stock dynamics in an Inceptisol of Indo-Gangetic Plain Zone of India. The
management of soil organic carbon (SOC) has now been identified as the most imperative dimension for
managing the global climate change as well as soil fertility. Long-term fertilization significantly
influenced SOC concentrations and storage to 60 cm depth. Below 60 cm, SOC concentrations and
storages were statistically not significant between all treatments. Organic manure plus inorganic fertilizer
application also increased labile soil organic carbon pools in 0–60 cm depth. The average concentration
of particulate organic carbon (POC), dissolved organic carbon (DOC) and microbial biomass carbon
(MBC) in organic manure plus inorganic fertilizer treatments (NP+S and NP+FYM) in 0–60 cm depth
were increased by 64.9–91.9%, 42.5–56.9%, and 74.7–99.4%, respectively, over the CK
treatment.Average SOC concentration of the control treatment was 0.54%, which increased to 0.65% in
the RDF treatment and 0.82% in the RDF+FYM treatment and increased enzyme activities, which
potentially influence soil nutrients dynamics under field condition. Compared to F1 control treatment the
RDF+FYM treatment sequestered 0.28 Mg C ha-1 yr-1 whereas the NPK treatment sequestered 0.13 Mg C
ha-1 yr-1. As tillage intensity increased there was a redistribution of SOC in the profile, but it occurred
only between ZT and PRB since under CT, SOC stock decreased even below the plow layer. Increased
SOC stock in the surface 50 kg m-2 under ZT and PRB was compensated by greater SOC stocks in the
50-200 and 200-400 kg m-2 interval under residue retained, but SOC stocks under CT were consistently
lower in the surface 400 kg m-2. Over the last 16 years, CT lost 0.83 ±0.2 kg of C m-2 while ZT gain 1.98
±0.3 and PRB gain 0.97±0.2 kg of C m-2 in the 1200 kg of soil m-2 profile. These results indicate that
long-term adoption of organic and conservation systems have the most beneficial effects in building
carbon sequestration potential and carbon stock pools among the investigated types of fertilization.
Keywords: Soil organic carbon fractions, C sequestration, soil aggregates, carbon dynamics
Introduction
Soil carbon sequestration at a global scale is considered the mechanism responsible for the
greatest mitigation potential within the agricultural sector, with an estimated 90%contribution
to the potential of what is technically feasible (Smith et al., 2008) [119]. However, global soil
carbon stocks of agricultural land have decreased historically and continue to decline (Lal,
2004a) [65]. Thus, improved agronomic practices that could lead to reduced carbon losses or
even increased soil carbon storage are highly desired. This includes improved crop varieties,
extending crop rotations, notably those with grass–clover or forage legume leys that allocate
more carbon below- ground, avoiding or reducing use of bare (unplanted) fallow (4), and the
application of organic fertilizer such as compost or waste products from livestock husbandry in
the form of slurry or stacked manure (5). Although these practices are not common in current
modern agriculture, they are core practices of organic agriculture, where crop production relies
in large part on closed nutrient cycles by returning plant residues and manures from livestock
back to the land and/or by integrating perennial plants, mainly grass–clover mixtures, into the
system. It is therefore hypothesized that the adoption of organic agriculture will lead to a
reduction in soil carbon losses or even to higher soil carbon concentrations and net carbon
sequestration over time (Niggli et al., 2009) [88].
With increasing global concerns over impacts of toxic chemicals, energy crisis and
environmental protection, it is becoming more alarming to rely on local abundant agricultural
bio resources than on chemical fertilizers. Recent studies have focused on reconsidering
cowpathy practices to enhance soil organic input, fostering agricultural sustainability by
promoting soil microbial biomass and activity. Conventional agro ecosystems have been
~ 2363 ~
Journal of Pharmacognosy and Phytochemistry characterized by high input of chemical fertilizer, leading to
deterioration of soil quality due to reductions in soil organic
matter and nutrients (Wu, 2009) [140]. Studies in comparison
with conventional agriculture systems reveals that organically
farmed soils showed improved soil quality with higher
microbiological activity, higher pH, organic C, N
mineralization potential, soil micro-organisms (30-40%), and
higher biological activity (30-100%).
Aggregate-size distribution and total organic carbon
Beare et al. (1994) [11] shown that conservationist soil
management practices can result in larger soil aggregation,
leading to increase in TOC stocks in the surface soil layer
when compared to conventional management practices, like
CT. The accumulation of TOC stocks under NT introduced
after continuous CT in the surface soil layer, down to
approximately 30 cm is a well known effect of NT and similar
conservation tillage systems. It is however subject to debate
whether NT is capable of accumulating more TOC if
investigated to larger depths. According to Baker et al. (2007)
[7] the ‘‘widespread belief that conservation tillage also favors
carbon sequestration may simply be an artifact of sampling
methodology’’ caused by shallow sampling. Sisti et al. (2004) [115] revealed that NT is in fact more efficient in organic
carbon stabilization to greater depths (to 100 cm), however
this is dependent on correct N management. Madari et al.
(2005) [76] found that the difference in SOC distribution
between aggregate-size fractions is greater under cultivation
than forest, regardless of the tillage system. Impacts of tillage
on SOC in different size fractions vary greatly because of
many factors, including climate, soil type, texture, pH and
dominant mineralogy. Adesodun et al. (2007) [1] also found
that the concentrations of SOC are higher under RNT than
CT, which implies that soil tillage management may play a
crucial role in sustaining agricultural productivity in this
system. The proportion of macro-aggregates (>1.00 mm) is
higher under RNT than CT, probably because tillage
disrupted soil macro-aggregates and reduced macro-
aggregates by 67% compared with RNT. The finding that
tillage methods do not change the distribution patterns of
SOC in aggregate-size fractions, but do change the size
distribution of aggregates, indicates that tillage influences soil
fertility through changes in soil structure. Onweremadu et al.
(2007) [91] reported that SOC in aggregates vary according to
tillage method. They found that the highest SOC was
distributed in 4.75–2.0 mm aggregates under MT, whereas
1.0–0.5 mm had the highest SOC under CT. Razafimbelo et
al. (2008) [107] report that SOC is mainly associated with
micro-aggregates (<0.02 mm) under NT with no significant
differences apparent for CT among macro-, meso- (0.02–0.2
mm), and micro-aggregates (<0.02 mm).
Source: Jiang et al. (2011)
Fig 1: Soil organic carbon and total N distribution in aggregates under different tillage regimes (RNT, combination of ridge with no tillage in a
rice rotation ecosystem; CT, conventional tillage in a rice rotation ecosystem)
Jiang et al. (2011) revealed that the highest SOC was
observed in the 1.00–0.25 mm size fraction (35.7 and 30.4
mg⁄ kg for RNT and CT, respectively), while the lowest SOC
was in the micro-aggregates and silt + clay fractions (19.5 and
15.7 mg⁄ kg for RNT and CT, respectively). While similar
distribution patterns were observed under RNT and CT, SOC
was significantly higher under RNT than CT by an average of
23.4%. One of the reasons for the significant difference may
be that the RNT system has greater crop residue production
resulting in higher residual returns to the soil each year. The
slower decomposition of this residue under RNT than CT is
due to less physical destruction during tillage and is also
likely to be responsible for the higher SOC levels under RNT.
The resulting higher crop and residue production is a response
to higher SOM levels, and higher nutrient-supplying capacity
of RNT soils compared with CT. Total N ranged from 1.3 to
3.0 mg⁄ kg, with an average of 2.3 and 2.13 mg⁄ kg for RNT
and CT, respectively. The highest total N for both RNT and
CT was in the 1.00–0.25 mm fraction while the lowest N for
both tillage methods was in the 0.25–0.053 mm fraction.
Similar to total C, total N was higher under RNT than CT.
Fig 2a: SOC levels in the 0–30 cm layer by tillage system CT, conventional tillage; MT, minimum tillage; NT, no tillage
~ 2364 ~
Journal of Pharmacognosy and Phytochemistry
Fig 2b: Vertical distribution of the SOC content in 2004 by tillage system
Sombrero and de Benito, (2010) [120] reported that at a depth
of 0–10 cm, the SOC content was significantly higher with
NT than CT or MT, by 58% and 11%, respectively. SOC
values were 41% higher with MT, in turn, than with CT. At a
depth of 10–20 cm, the SOC content was 30% higher with NT
than with CT and 7% higher than with MT. And at 20–30 cm,
it was 7% higher with MT than with CT, 12% higher with NT
than CT and 9% higher with no-till than minimum-till. In
2004, at the end of the 10 years period, SOC was 25% greater
with NT than CT, 16% greater with NT than MT, and 17%
higher with MT than CT (Figure 2 a & b). Onweremadu et al.
(2007) [91] also found that the highest SOC was distributed in
4.75–2.0 mm aggregates under MT, whereas 1.0–0.5 mm had
the highest SOC under CT. Razafimbelo et al. (2008) [107]
reported that SOC is mainly associated with micro-aggregates
(<0.02 mm) under NT with no significant differences
apparent for CT among macro-, meso- (0.02–0.2 mm), and
micro-aggregates (<0.02 mm). Chen and Shrestha (2012) [25]
observed that the SOC increased with the passage of time
(year) and caused an increase in percentage of water-stable
aggregate. Higher C accumulation in macro-aggregates could
be due to the lower decomposable SOM associated with these
aggregates and also the direct contribution of SOM to the
stability of macro-aggregates resulting in only C-rich macro-
aggregates being able to withstand slaking due to zeolitic
materials in the soil. Zhou et al. (2013) [143] concluded that the
application of NPK plus OM increased the size of sub-
aggregates that comprised the macro-aggregates. Also, they
observed that long-term application of NPK plus OM
improves soil aggregation and alters the three-dimensional
microstructure of macro-aggregates, while NPK alone does
not. Land use change usually alters land cover and the
terrestrial change in carbon stocks (Bolin and Sukumar,
2000). The change from one ecosystem to another can occur
naturally or through human activity. Anthropogenic changes
are prominent in tropical rain forest, which is a diverse and
complex ecosystem occupying approximately 17 percent of
the world’s land area and is a habitat for about 40 to 50% of
the earth’s species (Meyers, 1981). Tropical Rain Forests
represent significant sources/sinks of trace gases, and the
exchange of CO2 between forest and the atmosphere is an
important component of the global carbon cycle. The
economic damage through global warming from tropical
deforestation alone is estimated at $1.4-10.3 billion per year
(Pearce and Brown, 1994). Fearnside (1996) estimated the
economic damage by global warming in the region at
approximately $1,200 - $ 8,600 ha-1. In addition to its sheer
expanse, this eco-region also presents adequate climate
conditions for plant growth, expressed by high temperatures
throughout the year and well-distributed precipitation.
Therefore, tropical rainforest has, in principle, great potential
for soil carbon sequestration, despite poor to moderate soil
fertility.
Fig 3: Version of a land use/management sequence diagram
~ 2365 ~
Journal of Pharmacognosy and Phytochemistry Mamta et al. (2011) [78] reported that the fine (0.053–0.25
mm) intra-aggregate particulate organic C (iPOM-C), in 0.25-
to 2-mm aggregates, was also higher in ZT than conventional
tillage. A higher amount of macro-aggregates along with
greater accumulation of particulate organic C indicates the
potential of ZT for improving soil C over the long-term in
rice-wheat rotation Figure 4a. However, 0-5 cm layer, ZT had
significantly higher SOC of 7.37 and 7.86 g kg−1 in T5 and T6,
respectively than those of 5.81 and 6.14 g kg−1 in
conventional tillage treatments T1 and T2, respectively Figure
4b. This indicated a greater potential for C accumulation with
ZT likely to be associated with factors such as (a) a reduction
in soil disturbance, (b) undisturbed left –over stubbles on the
surface, and their slow decomposition leading to cooler soil
temperature, and (c) increased soil water retention (Kern and
Johnson, 1993) [57]. All of these favored the formation and
stabilization of soil aggregates and their associated organic C,
which has been protected from rapid breakdown and
decomposition (Six et al., 2000). Like rice, soil C at wheat
harvest was higher in ZT than conventional tillage.
Fig 4a: Intra-aggregate particulate organic matter (iPOM) C (g kg−1 of sand-free aggregates) in aggregate-size fractions at the 0- to 5-cm soil
depth at (i) rice and (ii) wheat harvest. ‘(a)’ and ‘(b)’ in legend refer to coarse (0.25–2 mm) and fine (0.053–0.25 mm) iPOM in the respective
size of aggregates
Fig 4b: Soil organic C (g kg−1 of bulk soil) as influenced by tillage practices at (a) rice and (b) wheat harvest
The CO2 is a major greenhouse gas (GHG) because of its
atmospheric concentration (about 398 ppm) and strongest
radioactive forcing among all the known GHGs (Figure 5),
despite having relatively lower warming potential (Forster et
al. 2007). It, along with atmospheric water vapors, contributes
majorly to the greenhouse effect on the earth. Though other
GHGs such as methane (CH4), nitrous dioxide (NOX) and
chlorofluorocarbons (CFCs) are present at lower
concentrations (about 2–6 orders of magnitude) than CO2 in
the atmosphere, their per molecule absorption of infrared (IR)
radiation is many fold higher than CO2. It is now known
(Figure 5) that the major contributors of the enhanced
atmospheric GHGs are fossil-fuel combustion, land use
changes and increased use of synthetic fertilizers in the
agriculture. The deterioration of soil quality following land
use change and agro-management practices has drawn global
attention towards the soil ecosystem in general and soil
organic carbon (SOC) dynamics in particular (Srivastava et
al. 2016a) [124]. It is believed that the increased atmospheric
CO2, in which land use change and management adds
considerably in the form of soil CO2 efflux, can be
sequestered back as SOC through appropriate agro-
management practices. It may help to mitigate the change in
global carbon cycle and climate (Aswathanarayana 2012) [3].
~ 2366 ~
Journal of Pharmacognosy and Phytochemistry
Fig 5: Major greenhouse gases (a) and their economic sector-wise (b) distribution (adapted and redrawn from IPCC 2014; USEPA 2014)
Singh et al., (2007) [114] have shown that addition of various
organic manures along with inorganic fertilizers in rice-wheat
system improved the aggregation status of the soil. Aggregate
ratio varied significantly with treatments. Compared with the
control, treatments where more organic matter was added
either through FYM, CR and GM maintained a greater
fraction of macro-aggregate. Bappa Das et al., (2014) [8]
revealed that the increased amounts of large (>2 mm) macro-
aggregate fractions in NPK + GR (rice) + FYM (wheat) and
NPK + CR (rice and wheat) are associated with the very large
MWD in these treatments. Similar trends are observed in
other organic treatments, with a large amount of small macro-
aggregate fractions, along with large macro-aggregates. A
higher amount of silt- and clay-sized fractions was observed
in the control (43.84%). Mazumdar et al., (2015) [81] found
that he MWD was significantly higher in plots receiving
50%NPK+ 50% N through FYM in rice (1.36 mm), 100%
NPK in wheat or 50%NPK+ 50% N through CR in rice (1.28
mm), 100% NPK in wheat or 50%NPK+ 50% N through GM
in rice (1.29), 100% NPK in wheat (1.18mm) as compared to
control (0.89 mm. Naresh et al., (2016) [85] revealed that the
small macro-aggregates accounted for >30% of the total
aggregates (mean of both main plots) in the surface soil layer.
Silt- plus clay-sized aggregates comprised the greatest
proportion of the whole soil, followed by the small macro-
aggregates. The amount of water-stable large and small
macro-aggregates in the FIRB and ZT plots were significantly
higher than in the CT plots in the 0- to 5-cm soil layer. These
differences may be attributed to the different planting
systems. Song et al., (2016) [122] reported that compared to
conventional tillage, the percentages of >2mm macro
aggregates and water-stable macro-aggregates in rice-wheat
double- conservation tillage (zero-tillage and straw
incorporation) were increased 17.22% and 36.38% in the 0–
15 cm soil layer and 28.93% and 66.34% in the 15–30 cm soil
layer, respectively. In surface soil (0–15cm), the maximum
proportion of total aggregated carbon was retained with 0.25–
0.106mm aggregates, and rice-wheat double-conservation
tillage had the greatest ability to hold the organic carbon
(33.64g kg−1)
Soil carbon dynamics and potential carbon sequestration
Soil C dynamics comprise the study of the soil C pools, the
rate of its exchange among them (turnover) and the associated
regulatory variables. Therefore, it encompasses the kinetics as
well as the governing variables, which defines the temporal
change in SOC pools among its various compartments. SOC
dynamics generally shows nonlinearity, and several years are
required to reach a new equilibrium. Therefore, the short-term
assessments misrepresent the SOC dynamics. However, the
long-term datasets to derive the rate of change across the
various SOC pools to better understand the SOC dynamics are
often scarce (Vaccari et al. 2012) [132].
Soil organic carbon is key attribute of soil fertility and
productivity because of its influence on the physical, chemical
and biological properties of soils. Irrespective of its potential
benefits to productivity and profitability, organic carbon
might be sequestered by vegetation and soils as a possible
way of reducing the rate of CO2 enrichment of atmosphere
and moderate the global climate change. Net change in SOC
depends not only on the current management practices but
also on the management history of the soil.
The presence of a positive difference in SOC concentrations,
stocks, and C sequestration rates between organic and
nonorganic systems does not reveal whether this change goes
along with a net carbon gain due to conversion from
conventional to organic farming or whether it rather reflects a
reduced carbon loss if compared with the non-organic
treatment. Leifeld and Fuhrer (2010) [68] found that an average
annual increase of the SOC concentration in organic systems
by 2.2%, whereas in conventional systems, SOC did not
change significantly. Freibauer et al. (2004) [41] estimated a C
sequestration potential of organic farming in Europe of 0–500
kg ha−1 y−1(more than 50% uncertainty) using calculations
based on the combination of single practices such as
intensification, improved rotations, residue incorporation, and
manure use, but excluding zero and reduced tillage.
~ 2367 ~
Journal of Pharmacognosy and Phytochemistry
Source: Houghton (2007)
Fig 6: Global carbon cycle depicting various pools and fluxes of C.
Land use change (LUC), especially forest to agriculture
conversion, has been identified as a major source of historical
loss of SOC, primarily in the form of soil CO2 efflux (Poeplau
and Don 2013) [102]. It strongly influences the balance of SOC
dynamics which affects the soil CO2 efflux and subsequent C
sequestration (Lal 2003). Further, various agro-management
practices differentially affect the SOC dynamics (Srivastava
et al. 2016a) [124]. These management- induced changes in the
SOC have been already studied well in agricultural systems in
the context of conservation tillage, cropping, organic and
synthetic fertilization, and residue incorporation (Srivastava et
al. 2016a) [124]. The intensive crop production practices to
increase the crop productivity (i.e. conventional agriculture),
which involves agro-chemicals, improved irrigation, high
mechanization and high yielding seed varieties, enhance the
soil C mineralization, but induce severe environmental
problems (Pimentel et al. 1995) [101]. Consequently, it depletes
SOC with the time because of continuous harvest and
negligible organic input. Therefore, it is essential to
understand various pools and processes related with SOC
before devising the management policies.
C entering the soil is slowly transformed to humus with the
remainder being mineralized back to CO2.
Dhama et al. (2005) [31] reported that degraded soil is
improved by layer of soil and bio-mass with sprinkling of
fresh dung slurry for composting. Cow dung along with sea
water and yeast has been exploited as a
liquid catalyst. It is claimed that it is capable of greening
degraded land. Not only good compost is made but valuable
organisms like earthworms are also generated as in due course
which keep on working all through. Individually or system as
a whole, biogas slurry with Panchgavya combination is
adjudged as the best organic nutritional practice for the
sustainability of crops by positive impacts on overall
performance on growth, productivity and soil health.
Rao et al. (2013) [108] revealed that, fertilizer application could
just maintain the status of soil organic carbon in the cropping
system, with neither improving nor declining at the end of the
annual cropping cycle. While it was found gradually built up
compared to the pre-experimental level, after all the three
crops raised with the application of organic manures. Among
the organic sources tried, neem leaf manure, Panchagavya,
vermicompost and farmyard manure added more organic
carbon to the soil compared to pig manure and poultry
manure. Slow decomposition of neem leaf, vermi compost,
farmyard manure and direct relation to improved fertility over
other manures may probably the reason for the differences in
soil organic carbon. Neverthless, organics did build up the
organic content as well as nutrients there by indicating the
sustenance of soil productivity [Table 1]. Ramesh and Rao
(2009) [105] also reported that soil health could be sustained
with organic nutrition due to diversification of soil biota.
Kamp et al. (2017) [54] revealed that cultivation over the years
caused a significant decrease in soil organic carbon content by
14% in unfertilized control as compared to uncultivated soil.
The balanced fertilization with NPK, super optimal dose of
NPK and integration of balanced fertilization with FYM
increased the SOC content as well as SOC stocks over the
initial year. The carbon sequestration potential (1.77 Mg ha-1)
was highest in 100%NPK +FYM treatment.
Table 1: Effect of various organic farming practices in maize-sunflower-green gram cropping system on soil organic carbon and apparent soil
nitrogen balance over two years
Treatments Organic carbon (%) Initial status
(kg/ha)
Added over two
years (kg/ha)
Uptake over two
years (kg/ha)
Final status
(kg/ha)
soil nitrogen
balance (kg/ha) 2004 2005
T1-No manure 0.21 0.18 135.6 0 154.5 100.6 -189.5
T2- Panchagavya 0.21 0.18 135.6 0 174.5 100.2 -209.9
T3-RDF 0.23 0.20 135.6 400 427.8 150.5 -12.9
T4-RDF + Panchagavya 0.23 0.20 135.6 400 434.1 149.7 -20
T5-Farm Yard Manure 0.42 0.48 135.6 400 410.7 193.1 46.8
T6-FYM + Panchagavya 0.42 0.48 135.6 400 447.8 191.2 7.8
~ 2368 ~
Journal of Pharmacognosy and Phytochemistry T7-Vermicompost 0.45 0.50 135.6 400 403.4 210.5 71.5
T8-T7 + Panchagavya 0.45 0.50 135.6 400 439 209.6 35
T9-Neem leaf manure 0.46 0.52 135.6 400 385.3 245.2 124.3
T10-T9 + Panchagavya 0.46 0.52 135.6 400 402.1 244.1 106.4
T11-Poultry manure 0.34 0.40 135.6 400 387.8 224.7 101.3
T12-T11 + Panchagavya 0.34 0.40 135.6 400 404.8 223.8 83.4
T13-Pig manure 0.34 0.40 135.6 400 407.4 208.1 65.1
T14-T13 + Panchagavya 0.34 0.40 135.6 400 442.6 205.9 27.7
Initial 0.23 0.32 - - - - -
C.D. (P = 0.05) 0.07 0.06 - - - - -
Soil Organic Carbon stock
Earth is a major reservoir of C. The lithosphere (i.e., the
geological strata) comprises of 75,004 Eg (Exagram =1018g =
1000 gigaton) of C or 99.938% of the total terrestrial C stock
(Lal, 2010). The non-geologic C component consists of 46.46
Eg or 0.062% of the total C stock. Of this ocean consists of
42Eg (Lal, 2010). In contrast, the entire atmospheric reservoir
contains merely 0.8Eg. Thus, even small changes in soil C
stock can have a major impact on the atmospheric
concentration of CO2.
Soil organic carbon stock is one of the most important
terrestrial pools for carbon storage. Onwudike (2010) [92]
reported that combination of cow dung with NPK (15:15:15)
in the concentration of 3 t/ha and 100 kg/ha, respectively. The
organic carbon of the soil after treatment with this
combination was found to be significantly increased from
1.33 to 3.21%. The combination also improved soil organic
matter, exchangeable ions, effective cation exchange capacity
and pH in comparison to untreated soil. Akhilesh and Nandan,
(2016) [5] found that soil organic carbon stock was found
maximum in treatment Dhanicha + FYM + Vermicompost
(Split) (43.77 tha-1), and highest rate of sequestration resulted
in Dhanicha + FYM + Vermicompost (Split) (2.69 tha-1yr-1).
Both these parameters were found minimum in Dhanicha in
kharif and no manure application in summer.
Eleanor et al. (2006) [34] reported that the SOC stocks for the
three dominant classes of cropping systems are shown in
Figure 7. They include rice-wheat, double-cropping (other
than wheat) with rice, and triple-cropping with rice. Double-
cropping refers to crop rotations with two crops grown in a
single year and triple cropping refers to crop rotations with
three crops grown in a single year. The SOC in double-
cropping systems that include rice in AESR’s 9.1, 9.2, and
13.1 will drop, due to shifts into other cropping systems and
losses of soil C resulting from cropping intensification. SOC
stocks in rice-wheat systems in those AESR’s will increase
substantially. AESR’s 2.3, 4.1, and 4.2 will see substantial
decreases in SOC stocks from rice-wheat systems as lands are
shifted out of rice-wheat and into triple cropping systems that
include rice.
Fig 7: SOC stock trends in dominant cropping system classes by AESR in the IGP
~ 2369 ~
Journal of Pharmacognosy and Phytochemistry Eleanor et al. (2006) [34] revealed that SOC stocks predicted
by Century, on a Tonnes-per-hectare basis, are shown in the
maps in Figures 8a, 8b and 8c for 1990 to 2030. Geographic
analysis of the stocks and change rates indicate a number of
contrasting effects that are occurring throughout the region. In
the lower IGP, cropping intensification has led to reductions
in SOC values in sandy, poorly drained soils. In contrast to
this, the central IGP has seen an increase in SOC in more
clayey soils, as has the upper IGP.
Naresh et al. (2017) [86] found that the quantities of SOC at the
0-400 kg of soil m-2 interval decreased under ZT without
residue (T1), PRB without residue (T4) and Conventional
tillage (T7) treatments evaluated. Stocks of SOC in the top
400 kg of soil m-2 decreased from 7.46 to 7.15 kg of C m-2
represented a change of -0.31±0.03 kg of C m-2 in T1, 8.81 to
8.75 kg of C m-2 represented a change of -0.06±0.05 kg of C
m-2 in T4, and 5.92 to 5.22 of C m-2 represented a change of -
0.70 ±0.09 kg of C m-2 in T7 between 2000 and 2016.
Fig 8a: SOC stocks predicted by the Century model in the IGP in
1990
Fig 8b: SOC stocks predicted by the Century model in the IGP in
2000
Fig 8c: SOC stocks predicted by the Century model in the IGP in
2030
Jobbágy and Jackson, (2000) [52] reported that the mean SOC
density invariably decreased with depth, its vertical
distribution pattern was notably different under different
LULC types. The mean SOC density under different LULC
types ranged from 6.0–11.3 kg·m−2 (0–20 cm), 3.9–6.4
kg·m−2 (20–40 cm), 2.5–3.7 kg·m−2 (40–60 cm), 1.5–2.5
kg·m−2 (60–80 cm) and 1.1–2.5 kg·m−2 (80–100 cm) (Table
2). The mean SOC density values at 0–20 cm and 20–40 cm
depths under all LULC types were significantly different from
each other and also from the values of the last three depths
The relatively large mean SOC density in the top layers could
be attributed to higher OM inputs by litter fall causing higher
accumulation of SOC in the upper layer of the mineral soil.
Table 2: Vertical distribution of SOC density values under different
land use/land cover (LULC) types
Depth
(cm)
SOC Density (kg·m−2) (Mean ± Standard Error Mean)
Agricultural
Lands Forests Grasslands Shrublands
0-20 5.98 ± 0.32 a* 9.62 ± 0.44 a 11.34 ± 1.05 a 8.73 ± 0.64 a
20-40 3.89 ± 0.32 b 6.35 ± 0.34 b 6.23 ± 0.75 a 5.58 ± 0.54 b
40-60 2.45 ± 0.36 c 3.73 ± 0.27 c 2.86 ± 0.61 b 2.53 ± 0.50 c
60-80 2.48 ± 0.34 c 2.54 ± 0.24 d 1.90 ± 0.95 b 1.49 ± 0.39 c
80-100 2.46 ± 0.34 c 2.50 ± 0.23 d 1.12 ± 0.00 b 2.05 ± 0.43 c
* Values in the columns suffixed with different superscript letters are
significantly different (p < 0.05) from each other.
Bäumler et al. (2005) [10] found that the vertical distribution of
SOC density under forests was more homogeneous than
grassland and shrublands (Figure 9a) probably due to high
OM inputs from both above- and belowground biomass, slow
decomposition and SOC complications with andic and spodic
properties of non-volcanic andosolic soils. Begum et al.
(2010) [14] observed that the mean SOC density under
different altitudinal zones was relatively large under 4000–
5520 m (4.8–13.2 kg·m−2 for first three depths) and 3500–
4000 m zones (3.4–11.7 kg·m−2) compared to 3000–3500 m
(2.2–11.6 kg·m−2), 2500–3000 m (1.7–7.0 kg·m−2) and
1769–2500 m zones (2.0–7.1 kg·m−2) (Figure 9b). The
increase in SOC density with altitudinal zone was largely due
to increase in SOC concentration with altitude resulting from
higher OM inputs from above- and belowground biomass,
slow decomposition due to low temperature [10] and more
translocation of OC into deeper layers.
~ 2370 ~
Journal of Pharmacognosy and Phytochemistry
Fig 9a: Proportion of SOC density (kg·m−2) stored at different depth
intervals under different LULC types
Fig 9b: Proportion of SOC density (kg·m−2) stored at different
depths under different altitudinal zones
Fig 9c: Proportion of SOC density (kg·m−2) stored at different depth
intervals under different aspect directions
Egli et al. (2009) [33] reported that the mean SOC density
values were variable in their ranges under different aspect
directions, viz: 2.8–10.6 kg·m−2 (north-facing slopes), 2.6–9.0
kg·m−2 (east-facing slopes), 1.9–8.5 kg·m−2 (south-facing
slopes) and 1.5–8.5 kg·m−2 (west-facing slopes) (Figure 9c).
At all depths, the northern aspect had relatively large mean
SOC density than other aspect directions. The larger SOC
density on the north-facing slopes could be ascribed to rich
biodiversity, high OM inputs, faunal abundance and more soil
moisture on the northern aspect compared to other aspect
directions. (Gathala et al. (2011b) [43] exposing SOC to
microbial decomposition compared to CT for wheat. The
cumulative carbon input from aboveground biomass after 7 yr
was about three times greater in ZTDSR-ZTW+R and
PBDSR-PBW+R than the other treatments, which increased
total SOC by 4.7 and 3.0 tha-1 at 0–0.6 m depth, respectively.
Bhattacharyya et al. (2000a) [16] revealed that the SOC stock
of the IGP constitutes 6.45% of the total SOC stock of India,
0.30% of the tropical regions and 0.09% of the world in the
first 30 cm depth of soils. The corresponding values for SIC
are 3.20% for India, 0.17% for tropical regions and 0.06% for
world, respectively Table 3. Therefore it indicates that IGP
has only 3% SOC stock of the country. The impoverishment
of SOC in the IGP as compared to tropical regions and world
in general and to India in particular is thus apparent.
Table 3: Carbon stock in IGP, India and other regions
Region IGP, India
Soil depth range (cm)
0-30 0-100 0-150
<————————— Pg———————————>
SOC 0.63 (6.45/0.30/0.09)* 1.56 (6.23/0.39/0.10)* 2.00 (6.67/0.32/0.08)*
SIC 0.13 (3.20/0.17/0.06)* 1.96 (8.76/0.93/0.27)* 4.58 (—/—/—)*
Total 0.76 (5.50/0.27/0.0.08)* 3.52 (7.42/0.58/0.16)* 6.58 (10.28/—/—)*
India1
SOC 9.77 25.04 29.97
SIC 4.06 22.37 34.03
Total 13.83 47.41 64.00
Tropical Regions2
SOC 207 395 628
SIC 76 211 —
Total 283 604 —
World2
SOC 704 1505 2416
SIC 234 722 —
Total 938 2227 —
* Values in parentheses indicate% of stock in India, Tropical Regions and the world respectively,
- = figures not available 1Bhattacharyya et al. (2000a) [16]
~ 2371 ~
Journal of Pharmacognosy and Phytochemistry Paudel et al., (2014) [98] showed that, soil organic carbon
buildup was affected significantly by tillage and residue level
in upper depth of 0-20 cm but not in lower depth of 20-40 cm.
Higher SOC content of 19.44 g kg-1 of soil was found in zero
tilled residue retained plots followed by 18.53 g kg-1 in
permanently raised bed with residue retained plots. Whereas,
the lowest level of SOC content of 15.86 g kg-1 of soil were
found in puddled transplanted rice followed by wheat planted
under conventionally tilled plots. Pandey et al., (2014) [98]
revealed that no-tillage before sowing of rice and wheat could
increase SOC by 0.59 Mg C ha–1yr–1. The rate of SOC
sequestration due to reduced- or no-tillage management in
rice-based systems in South Asia varied from 0- to 2114 kg
ha–1 yr–1 (Bhattacharyya et al., 2012a) [19]. Naresh et al.,
(2015) [84] revealed that the highest SOC stock of 72.2Mg C
ha-1 was observed in F4 with T6 followed by that of 64Mg C
ha-1 in F6 with T2> that in F3 with T4 (57.9Mg C ha-1)> F5 with
T1 (38.4Mg Cha–1) = F7 with T5 (35.8Mg C ha-1), and the
lowest (19.9Mg C ha-1) in F1 with T7. Relatively higher
percentage increase of SOC stock was observed in F4 with T6
treatment (56.3Mg Cha-1) followed by F6 with T2 (51.4Mg
Cha-1) and F3 with T1 (48.4Mg Cha–1).
Venkanna et al. (2014) [133] reported that the soil organic
carbon (SOC) stock was highest in Alfisols (52.84 Mg ha–1)
followed by Inceptisols (51.26 Mg ha–1) and Vertisols and
associated soils (49.33 Mg ha–1), whereas soil inorganic
carbon (SIC) stock was highest in Vertisols and associated
soil (22.9 Mg ha–1) followed by Inceptisols (17.5 Mg ha–1)
and Alfisols (12.4 Mg ha–1). The total organic carbon stock
has
been estimated as 0.068 Pg for 0–60 cm soil depth and the
organic C stock with categories < 40 Mgha–1, 40– 50 Mg ha–1,
50–60 Mg ha–1 and > 60 Mg ha–1 are 5.19%, 20.36%, 57.92%
and 16.53% respectively. For inorganic carbon stock it is
estimated to be 0.02 Pg with categories < 10 Mg ha–1, 10–20
Mg ha–1, 20–30 Mg ha–1 and > 30 Mg ha–1 as 6.14%, 68.11%,
18.46% and 7.28% respectively, for 60 cm soil depth Figure
10a. Relationship between inputs of SOC with SOC stock.
The input of SOC has been estimated based on biomass yield,
input of organic residue, including FYM, fertilizers and leaf
fall to soils. The input of organic matter is also well correlated
with organic carbon stock. The C saturation level in the soil of
semiarid tropics is estimated to be 73.21 Mg ha–1 up to 60 cm
soil depth Figure 10b.
Fig 10a: Distribution of carbon stock (total, organic and inorganic) in Alfisols, Inceptisols and Vertisols and soils for 0–60 cm soil depth
Fig 10b: Soil organic carbon stock (Mg ha–1) expressed as a function of carbon input levels (Mg ha–1yr–1) for the semiarid tropical region of
South India
Naresh et al. (2015) [84] observed that compared to the RDF
treatment also, the RDF+FYM treatment had higher SOC
concentration in all the TCE. The highest increase in SOC in
the RDF+FYM treatment was observed in F4 with TCE T6
(Table 4). Organic sources of nutrient such as FYM
decompose slowly resulting in more SOC accumulation in
soil (Lu et al., 2009) [74]. In comparison with the control, the
mean rate of SOC build-up during the 12 years of cropping
was the highest in F6 with T6 (50.63%) and the lowest in F7
with T7 (16.48%). It was estimated that 30 per cent of applied
C through FYM was stabilized, and the rest (70 per cent) was
lost through oxidation. Although ploughing- induced
depletion of SOC pool is widely observed (Bhattacharyya et
al., 2011) [18], the magnitude of depletion depends upon the
geographical location, crops/ cropping systems and inherent
soil properties (Mandal et al., 2007) [79].
~ 2372 ~
Journal of Pharmacognosy and Phytochemistry Table 4: C restoration rate in soil profile as affected by 12 yr of tillage crop establishment and fertilization
Source: Naresh et al. (2015) [84]
T1- CTDSR-ZTDSW; T2- CTTPRAWD–ZTDSW; T3-
ZTDSR-ZTDSW; T4- ZTTPR-ZTDSW;
T5- WBedDSR- WBedZTDSW; T6- WBedTPR-
WBedZTDSW; T7- CTTPR-CTDSW; F1-Control (no N–P–K
fertilizers or organics; F2- 50% RDF; F3-100% RDF; F4-100%
organic as sole FYM;F5- 50% RDF+50% RDF (foliar); F6-
50% organic (FYM) + 50%RDF; F7- Farmer’s practice (180
kg N + 60 kg P2O5 ha–1 only)
Soil carbon sequestration
Carbon sequestration is the provision of long-term storage of
carbon in the terrestrial biosphere, underground, or in the
ocean so that the buildup of carbon dioxide (the principal
greenhouse gas) concentration in the atmosphere will reduce
or slow down. It is also known as carbon capture and storage.
Agriculture is defined as an anthropogenic manipulation of
carbon through uptake, fixation, emission and transfer of
carbon among different pools. Thus land use change, along
with adoption of recommended management practices can be
important instrument of soil organic carbon (SOC)
sequestration (Post and Kwon, 2006) [103]. Soil organic carbon
sequestration (SOCS) is a process in which carbon dioxide
(CO2) is removed from the atmosphere and stored in the soil
carbon pool. This process is primarily mediated by plants
through photosynthesis, with carbon stored in the form of
SOC (Ontl and Schulte, 2012) [90]. Carbons stored in soils
represent the largest terrestrial carbon pool and factors
affecting this will be vital in the understanding of future
atmospheric CO2 concentrations in the climate change arena.
After 16 years of different fertilization treatments in the crop
rotation, Liu et al. (2005) found that the profile average SOC
content (0–90 cm) was only 0.9%, 4.1%, and 8.6% higher for
manure, chemical fertilizers, and manure plus fertilizers,
respectively, than that with no fertilizer application or control.
However, SOC at the 0–15 cm soil layer was 6.2%, 7.7%, and
9.3% higher with manure, chemical fertilizers, and manure
plus fertilizers, respectively, than with no fertilizer
application. Yang et al. (2003b) indicated that the SOC
content could be maintained at a relatively stable level under
sufficient chemical fertilizer application without return of
manure and crop residue conditions, and SOC content was
increased at the combination of chemical fertilizer and
manure application. Francioso et al. (2000) also reported that
SOC and N differed significantly after 22 years for all
treatments where the amendments with cattle manure
markedly increased the SOC and N contents, while cow
slurries and crop residues reduced SOC and N contents.
Soil carbon sequestration is a process in which CO2 is
removed from the atmosphere and stored in the soil carbon
pool. This process is primarily mediated by plants through
photosynthesis, with carbon stored in the form of SOC. In arid
and semi-arid climates, soil carbon sequestration can also
occur from the conversion of CO2 from air found in soil into
inorganic forms such as secondary carbonates; however, the
rate of inorganic carbon formation is comparatively low (Lal,
2008) [66].
Fig 11a: Change in soil organic C in the NPK+FYM treatment compared to the NPK treatment in various long-term experiments
~ 2373 ~
Journal of Pharmacognosy and Phytochemistry
Fig 11b: Sequestration of C with change in net return in the NPK+FYM treatment compared to the NPK treatment in various long-term
experiments
Pathak et al. (2011) [97] revealed that compared to the NPK
treatment also, the NPK+FYM treatment had higher SOC
concentration in all the LTEs (Figure 11a). The highest
increase in SOC in the NPK+FYM treatment was observed in
LTE 14 in New Delhi (Figure 11b). Organic sources of
nutrient such as FYM decompose slowly resulting in more
SOC accumulation in soil (Mandal et al., 2007) [79]. High
lignin content in FYM resulted in greater accumulation of C
compared to other non-lignin materials (Paustian et al., 1992) [99]. Carbon sequestration in CSP NPK scenario denoted that
even without any organic matter application soils could
sequester organic carbon through balanced application of
NPK. But application of FYM along with inorganic fertilizer
led to an additional build up of SOC in soil. Average rate of
sequestration was 0.33MgC ha−1 yr−1 in the NPK+FYM
treatment whereas in the NPK treatment the rate was
0.16MgC ha−1 yr−1. The C sequestration rate was lowest in
LTE 18 in the NPK treatment (0.02MgC ha−1 yr−1) whereas it
was highest in LTE 25 (1.2MgC ha−1 yr−1) in the NPK+FYM
treatment. In the INM scenario i.e., NPK+FYM treatment
compared to the NPK treatment, the average C sequestration
rate was 0.17%. The study showed that C sequestration in
Indian agricultural soil was feasible with application of NPK
and FYM. Addition of about 10Mg FYM ha−1 sequestered
0.33 Mg C ha−1 yr−1. However, to apply this magnitude of
FYM to 147.43Mha agricultural land the country would
require 1474Mt of FYM per year (737 Mt dry weight
considering 50% moisture content). India supports the largest
bovine (cattle + buffalo) population (286.22 million) of the
world (MAC, 2006). In the country 335Mt dung is produced
per annum out of which 110Mt is lost during collection or
used for construction purposes (Pathak et al., 2009) [96].
The remaining 225Mt dung is available for use in agriculture.
This is only about 1/3rd of the FYM requirement of the
country to achieve the full potential of C sequestration. There
are, however, some other sources of organic C, which can be
used in agriculture for C sequestration. For example, total
municipal solid waste (MSW) generation from major Indian
cities (35 metro cities and 24 state capitals) is about 40
thousand Mgd−1 (CPCB, 2006). The biodegradable organic
matter in MSW is about 28% by mass. Thus MSW from
Indian cities generates 4.1Mt C yr−1 and can be an important
source of organic C (Pathak et al., 2009) [96]. Chan, (2008)
reported that globally, clearing natural vegetation for
agriculture results in large reductions in SOC levels and
further declines may occur due to management practices. In
many areas, soil carbon levels have dropped by up to 50%
compared to pre-agricultural periods. Most of the reduction in
SOC occurs in the surface soil layer, 0–10 cm. Therefore, soil
carbon levels of agricultural soils are lower than
corresponding soils under natural vegetation. This difference
in SOC indicates the potential for soil carbon storage.
Xu, (2008) [141] revealed that the estimation of total topsoil
SOC sequestration of (29.9± 61.1) to (31.3±72.4) Tg per year
for the period of 1980-2006, among which (9.15±14.0) Tg/a is
contributed by rice paddies and the other (25.7±61.4) Tg/a by
dry croplands. Depletion of SOC stocks has created a soil
carbon deficit that represents an opportunity to store carbon in
soil through a variety of land management approaches.
However, various factors impact potential soil carbon change
in the future, including climatic controls, historic land use
patterns, and current land management strategies. Continued
increases in atmospheric CO2 and global temperatures may
have a variety of different consequences for soil carbon inputs
via controls on photosynthetic rates and carbon losses through
respiration and decomposition. Carbon loss may also increase
due to increased plant respiration from greater root biomass
(Hungate et al. 1997) [47], or from accelerated decomposition
of SOM through increased microbial activity (Zak et al.
2000).
Likewise, increased temperatures may impact the carbon
balance by limiting the availability of water, and thus
reducing rates of photosynthesis. Alternatively, when water is
not limiting, increased temperatures might increase plant
productivity, which will also impact the carbon, balance
(Maracchi et al. 2005). Estimates of the global sequestration
potential of agricultural soils are typically made for
sequestration on an annual basis and range from 0.4 to 1.2
gigatons per year (Gt/yr) (Lal, 2004a) [65]. Some are more
optimistic, including Kell (2011, 2012) [55, 56] who argues that
by improving root growth in agricultural crops, soil carbon
storage could match anthropogenic emissions for the next 40
years. When multiplied across several years, these rates
produce vastly different estimates of the total potential of soil
carbon sequestration. An optimistic soil carbon accrual rate
could sequester at least 10% of the current annual emissions
of 8-10 Gt/yr (Hansen et al., 2013) [44], while a lower rate
would account for less than 5%. If deep rooted crops could be
elevated and bred, that potential might be even greater.
Hossain (2009) [45] reported that the greater SOC content
under poultry litter and cattle manure application in rice-
wheat-legume rotation compared to farmers’ practice of no
manure and fertilizer application in the rice-wheat-fallow
system in Bangladesh. Similarly, manure or straw addition
when combined with NP fertilizer increased SOC content by
0.30 Mg ha–1yr–1 in a rice-wheat rotation (Fang et al. 2005).
Majumder et al. (2008) [77] indicated that application of NPK
and organic amendments (FYM, straw, and green manure)
~ 2374 ~
Journal of Pharmacognosy and Phytochemistry could increase SOC by 24%. Jha et al. (2013) [51] also found
that an application of bio-nutrient containing Pseudomonas
mycostraw, cyanobacteria, and Azospirillum increased SOC
by 14 to 18% in a rice field in Bihar, India. Sapkota et al.
(2017) [111] revealed that after seven years, ZTDSRZTW+R
and PBDSR-PBW+R increased SOC at 0–0.6 m depth by 4.7
and 3.0 t Cha-1, respectively, whereas the CTR-CTW system
resulted in a decrease in SOC of 0.9 tC/ha. Over the same soil
depth, ZT without residue retention (ZTDSR-ZTW) only
increased SOC by 1.1tCha-1.
Table 5: SOC sequestration rates of croplands of some countries (Data calculated from the literature)
Country Contemporary/(Tg/a) Future potential
Global soil Not applicable 0.2-1.0 Tg/a Cambell, (2003), 1.2-2.6 Pg/a Lal, (1999)
Global agricultural soil 75-1140 1.3-1.5 Pg/a Smith et al. (2008) [119],0.4-0.6Pg/a Cambell, (2003)
EU agricultural soil 56 80-100 Tg/a (biophysical) Smith,(2004) [117],16-19 Tg/a (reachable) Smith et al.
(2005) [116, 118]
USA agricultural soil 67.3 83 Tg/a Sperow et al. (2003)
Indian agricultural soil Not applicable 6-7 Tg/a Lal, (2004)
China’s agricultural soil 34 66.7 Tg/a Xu, (2008) [141]
Dynamics of Soil Organic Carbon Stock
Soil organic matter is made up of four major pools—plant
residues, particulate organic carbon, humus carbon and
recalcitrant organic carbon. These pools vary in their
chemical composition, stage of decomposition and role in soil
functioning and health. Management is capable of altering not
only total organic carbon stocks, but the proportion of carbon
present in these different pools. Knowledge of how carbon
pools change in response to management can provide valuable
information on likely soil functioning and health. Naresh et
al. (2015) [84] reported that the highest SOC stock of 72.2Mg
C ha”1 was observed in F4 with T6 followed by that of 64Mg
C ha-1 in F6 with T2 > that in F3 with T4 (57.9Mg C ha–1)> F5
with T1 (38.4Mg C ha–1) = F7 with T5 (35.8Mg C ha-1), and
the lowest (19.9Mg C ha-1) in F1 with T7. Relatively higher
percentage increase of SOC stock was observed in F4 with T6
treatment (56.3Mg C ha–1) followed by F6 with T2 (51.4Mg C
ha–1) and F3 with T1 (48.4Mg C ha–1) Table 6. Majumder et
al., (2008) [77] reported 67.9% of C stabilization from FYM
applied in a rice–wheat system in the lower Indo-Gangetic
plains. It is well recognized that improved management
practices promote soil carbon sequestration, and thus increase
soil carbon storage (Lu et al., 2009) [74].
Table 6: Profile soil organic carbon (SOC) as affected by 12 yr of tillage crop establishment and Fertilization
Source: Naresh et al. (2015) [84]
Rahangdale and Pathak, (2016) [104] reported that among the
land uses, the mean SOC content was highest (0.81%) in
eucalyptus+pigeonpea agrisilviculture practice followed by
eucalyptus+paddy-wheat (0.77%), eucalyptus+moong-wheat
(0.76%), eucalyptus+soybean-mustard (0.74%), eucalyptus
sole plantation (0.71%), pigeonpea (0.68), paddywheat
(0.66%), soybean-mustard (0.65%) and mean SOC content
was lower under moong-wheat conventional cropping land
use system (0.62%) [Table 7]. The SOC content also varied
with soil depth. Significantly, highest value of 0.79% was
recorded in the top soil layer (0-15 cm) followed by mid layer
(15-30 cm) and lower layer (30-45 cm), which showed
gradually decreasing trend in soil depth. Highest SOC content
in upper most soil layer (0-15 cm) was reflecting the highest
root densities and increased biological activity (Nair and
Chamuah, 1988). The integration of tree under farming
systems always had highest SOC content over the
conventional cropping system which may be attributed to
addition of litter-fall and root residues of both crops and trees.
On account of recycling of organic matter, higher organic
carbon contents were observed in the soil under intercropped
poplar plantations than at a site without trees and the content
varied depending upon the intercrops (Moshin et al. 1996) [83].
The lower SOC content in conventional sole cropping land
use systems is attributed due to the lower amount of residues
addition to soil. This is because SOC content varies with the
extent and type of vegetative cover on the land as quoted by
Koul et al. (2011) [58].
Rahangdale and Pathak, (2016) [104] also found that the SOC
stock and CO2 sequestration (CS) potential were significantly
influenced by different land use systems and soil depth. Mean
SOC stock (16.33 t ha-1) and CS potential (59.92 t ha-1) both
were found significantly higher under eucalyptus+pigeonpea
agrisilviculture practice followed by eucalyptus+paddy-wheat
[15.66 t ha-1 (SOC stock) and 57.48 t ha-1 (CS potential)],
eucalyptus+moong-wheat [15.61 t ha-1 (SOC stock) and 57.27
t ha-1 (CS potential)], eucalyptus+soybean-mustard [15.41 t
ha-1 (SOC stock) and 56.57 t ha-1 (CS potential)], eucalyptus
sole plantation [14.74 t ha-1 (SOC stock) and 54.11 t ha-1 (CS
potential)], soybean-mustard [14.12 t ha- 1 (SOC stock) and
~ 2375 ~
Journal of Pharmacognosy and Phytochemistry 51.84 t ha-1 (CS potential)], paddy-wheat [14.19 t ha-1 (SOC
stock) and 52.06 t ha-1 (CS potential)], pigeonpea [14.39 t ha-1
(SOC stock) and 52.80 t ha-1 (CS potential)] and lower
magnitude was found under moong-wheat conventional
cropping [13.71 t ha-1 (SOC stock) and 50.30 t ha-1 (CS
potential)] [Table7]. The highest SOC stock and CS potential
under eucalyptus+pigeonpea agrisilviculture practice may
have happened because of enhanced accumulation of leaf
litter in tree based agroforestry land use systems. The
abundant litter and or pruned biomass return to soil, combined
with the decay of root, contribute to the improvement of
organic matter under complex land use systems (Beer et al.,
1990 and Kumar et al., 2001) [12, 60]. Low amount of soil
organic carbon stock under the conventional agriculture land
system can be ascribed to intensive cropping as also reported
by Lal et al., (1998) and Bhardwaj et al. (2013) [15].
It was also observed that, the SOC stock and CS potential in
the soil also varied with its depth. Maximum of 16.08 and
59.00 t ha-1 was recorded in the top layer (0-15 cm), while the
minimum of 13.71 and 50.33 t ha-1 was recorded at the lower
layer studied (30-45 cm). This gradually decreased
significantly with increasing soil depth. The increase or
decrease in SOC stock and CS potential was associated with
bulk density and organic carbon content of soil at a particular
soil depth. The higher amount of SOC stock and CS potential
in surface layer i.e., 0-15 cm may be explained in the sense
that, there is continuous accumulation of leaf litter on the
surface layer which keep on decomposing and thus enrich the
upper layer continuously. Carbon stock is also intricately
linked with site quality, nature of land use, choice of species
and other management practices adopted, which explains the
varying carbon stock in different land use management and
also at different soil depths. This in turn is due to the effect of
differential litter addition in different land uses (Swamy et al.
2003) [128]. Thus accumulation of SOC stock in different land
uses through litter fall is different that might have been
regulated due to varying organic matter decomposition and
the formation of stable and labile soil organic matter pool in
these land uses (Vitousek and Sanford, 1986) [134].
Table 7: Effect of land use systems and soil depth on soil organic carbon stock
Land Use Systems Soil organic carbon stock (t ha-1) CO2 sequestration potential (t ha-1)
0-15 15-30 30-45 Mean 0-15 15-30 30-45 Mean
Paddy-wheat conventional cropping 15.17 14.42 12.97 14.19 55.66 52.93 47.60 52.06
Soybean - mustard conventional cropping 15.26 14.15 12.97 14.12 55.99 51.94 47.58 51.84
Moong -wheat conventional cropping 14.67 13.71 12.74 13.71 53.83 50.31 46.77 50.30
Pigeonpea conventional cropping 15.37 14.59 13.21 14.39 56.39 53.55 48.47 52.80
Eucalyptus sole plantation 15.62 14.90 13.71 14.74 57.32 54.68 50.32 54.11
Eucalyptus + paddy- wheat agrisilviculture 17.26 15.42 14.31 15.66 63.33 56.61 52.51 57.48
Eucalyptus+soybean-mustard agrisilviculture 16.48 15.32 14.45 15.41 60.48 56.21 53.03 56.57
Eucalyptus + moong- wheat agrisilviculture 16.94 15.49 14.38 15.61 62.18 56.85 52.79 57.27
Eucalyptus + pigeonpea agrisilviculture 17.93 16.36 14.69 16.33 65.81 60.04 53.92 59.92
Mean 16.08 14.93 13.71 - 59.00 54.79 50.33 -
Land use system C.D. at 5% 0.42 1.55
Soil Depths C.D. at 5% 0.24 0.89
Interaction (Land use systemX Depth) C.D. at 5% NS NS
Soil organic carbon storage
An estimate of 1500 Pg SOC and about 2000 Pg SIC had been
generally accepted for world soils. Among the global
terrestrial C pools, the SOC pool of the agricultural soils has
been regarded as most prone to change and would be
modified in short term under human management practices
(FAO, 2001) [39]. The size of this pool and the capacity for
future sequestration has been one of the important baselines
for assessing global capacity of CO2 offsetting for the recent
years. Globally, the soil area under agriculture amounts to
5000 Mhm2, of which about 1400 Mha is used for crop
production in a proportion of 10.5% to the global land area
(FAO, 2001) [39]. Therefore, the C turnover of these
agricultural soils could have deep impact on global terrestrial
C cycling and climate change.
Table 8: SOC pool and storage of some representative countries (data cited or calculated from literature)
Region Whole soil/ Pg Topsoil/ Pg Topsoil storage/ (t/hm2) Reference
Globe 1500 684 46.91), 47.82) Batjes, (1996)
USA - - 50.3 US Climate Change Sci Prog. (2007)
EU - 34.6 70.8 Smith et al. (2004) [117]
Brazil - 36.4±3.4 44.1 Bernoux et al. (2002)
India 63.2 (150 cm) 21.0 63.8 Bhattacharyya et al. (2000) [16]
China 90 43.6 46.7±44.3 Song et al. (2005) [121]
Notes: 1) According to the global land area of 146.6 Mkm2; 2) According to the total exposured land area of 143.2 Mkm2
Feng and Li (2001) [37] in their 5 years study concluded that
for the same carbon input, carbon storage in soil was higher
by 1.18 t/ha C with manure application than with plant
residues. Kukal et al. (2009) [59] conducted two long term
experiments involving application of FYM and inorganic
fertilizer in rice-wheat and maize-wheat cropping systems.
They reported that the SOC sequestration rate was higher in
FYM plots in comparison to NPK plots in both the cropping
systems. Also the sequestration rate was three times higher in
rice-wheat than in maize-wheat cropping system. In rice-
wheat system, the FYM plots sequestered 0.31 Mg/ha/year
while the rate was 0.14 Mg/ha/year in maize-wheat cropping
system. This was due to that the soil in rice-wheat cropping
system was under submerged condition for three to four
~ 2376 ~
Journal of Pharmacognosy and Phytochemistry months and lack of oxygen for microbial activities resulted in
slower rate of decomposition. Secondly, the biomass
production was higher in rice in comparison to maize. They
also found that at all the sampling depth; the magnitude of
difference among treatments was greater in the top soil (0-15
cm) layer and generally decreased with soil depth. This was in
consonance with the studies conducted by Parker et al. (2002) [95] who obtained 7-20% higher organic carbon in top soil
layer (5 cm) in cotton-rye cropping system with poultry litter
as compared to fertilizer. Conservation practices such as
reduced- and no-tillage are interlinked with crop residue and
nutrient management (fertilizers, manure, and green
manures), which influences SOC accrual and C dynamics in
cropping systems (Ladha et al. 2011; Ghimire et al. 2012) [67,
42].
Soil organic carbon pool
The depletion of the SOC pool leads to a downfall in the soil
quality and productivity. SOC consists of several pools,
namely active, slow and passive, with differential turnover
rate ranging from months to over several hundred to
thousands years (Silveira et al. 2008) [113]. Active SOC pool
plays a very different role than passive does. As labile (active)
and non-labile (stable) SOC play differential roles in SOM
dynamics and nutrient cycling, the pool size and turnover time
of these two fractions in bulk soil and in aggregate size
fractions may be important to assess and evaluate the soil
management practices for the monitoring of SOC (Srivastava
et al. 2016b) [125]. Ch. Srinivasarao et al. (2011) [26] reported
that the surface 0.2m layer, 50 per cent RDN (F) + 50 per cent
RDN (FYM) contained the highest SOC concentration (2.7 g
kg-1) followed by that in 50 per cent RDN (FYM) (2.2gkg-1)
and 100 per cent RDN (F) (1.7 g kg-1). There was a significant
reduction in SOC concentration with the sole application of
inorganic fertilizers (100 per cent RDN) compared with those
in the mixed organic and inorganic or sole FYM treatments
Table 9. Ch. Srinivasarao et al. (2012) [27] also found that in
comparison with the control,% increase in SOC stock was in
the order 100% organic (FYM) treatment (55.0) > 50%
organic (FYM)+50% RDF (35.2) > 100% RDF (mineral)
(15.3).This trend was reflected in the profile SOC stock of the
respective treatments. The mean rate of change in SOC stock
followed a trend similar to that of SOC stock (Table 9). The
SOC stock declined in all but two treatments (100% FYM,
50% FYM + 50% RDF). The mean rate of SOC sequestration
in two treatments which enhanced SOC stock over 21 yr was
0.32 Mg ha–1 yr–1 for 100% FYM and 0.15 Mg ha–1 yr–1 for
50% FYM + 50% RDF. However, results showed that 13.4%
C applied as FYM was stabilized in SOC stock. Similarly,
Majumder et al. (2008) [77] reported 67.9% of C stabilization
from FYM applied in a rice–wheat system in the lower Indo-
Gangetic plains.
Table 9: Changes in concentration of soil organic carbon after 18 years of cropping and use of amendments (Mean ±SD)
Source: Ch. Srinivasarao et al. (2011) [26]
Source: Trumbore, (1997)
Fig 12: Characteristics of different soil organic C pools and soil CO2 efflux
~ 2377 ~
Journal of Pharmacognosy and Phytochemistry Table 10: Profile soil organic carbon (SOC), C restoration, C restoration rate, and C sequestered in soil profile as affected by 21 yr of cropping
and fertilization under sub-humid tropical conditions (± standard deviation from mean).
Source: Ch. Srinivasarao et al. (2012) [27]
Nayak et al. (2012) [87] reported that improved the SOC,
particulate organic carbon (POC), microbial biomass carbon
(MBC) concentration and their sequestration rate. Application
of 50% NPK + 50% N through FYM in rice and 100% NPK
in wheat, sequestered 0.39, 0.50, 0.51 and 0.62 Mg C ha−1 yr−1
over control (no N–P–K fertilizers or organics), (Figure 13 a,b
&c). Across the different agro-climatic zones of IGP, higher
SOC content was observed in Kalyani (LGP) followed by
Sabour (MGP), Kanpur (UGP) and Ludhiana (TGP),
respectively. Across all the agro climatic zones, the
sequestration rate of SOC, POC and MBC in all the four
treatments followed the order NPK + FYM > NPK + CR >
NPK + GM > NPK.
Ch. Srinivasarao et al. (2011) [26] revealed that the profile
SOC stock was the highest in 50 per cent RDN (F) + 50 per
cent RDN (FYM) (25.5MgCha_1) followed by that in the 50
per cent RDN (FYM) (23.4MgC ha_1), and the lowest in the
control (17.9MgCha_1) (Table 10). The highest rate of SOC
build-up from the C inputs was observed in treatments
receiving 50 per cent RDN (F) + 50 per cent RDN (FYM)
(42.5 per cent) followed by that in the 50 per cent RDN
(FYM) (30.7 per cent), farmer’s practice (10.6 per cent), 100
per cent RDN (F) (7.8 per cent), and the lowest in 50 per cent
RDN (F) (7.3 per cent). A similar trend was also observed in
the profile SOC stock and the rate of SOC build up in the
respective treatments.
Fig 13(a): Soil organic carbon sequestration (Mg ha−1 yr−1)
Fig 13(b): Particulate organic carbon sequestration (Mg ha−1 yr−1)
~ 2378 ~
Journal of Pharmacognosy and Phytochemistry
Fig 13(c): Microbial biomass carbon sequestration (Mg ha−1 yr−1) in different inte-grated nutrient management system over the control under
different agro-climatic situation in Indo-Gangetic Plains
Table 11: Cumulative C input, profile SOC, C build up, C build up rate and C sequestered in soil profile as affected by 18 years of cropping and
fertilization under semi-arid conditions (Mean± SD)
Source: Ch. Srinivasarao et al. (2011) [26]
Microbial Biomass
Microbial biomass is considered as a crucial parameter to
evaluate the functional status of soil. The top soil layer had
higher amount of MBC than the deeper layer, because the
amount of microbial biomass and rate of microbial activity
decline rapidly below the surface layer. Soil microbes play
crucial roles in soil ecosystems by regulating the
decomposition of organic matter, the formation of humus, and
cycling of nutrient elements, while soil enzymes catalyze or
mediate most soil biological processes; thus, soil microbes
and enzymes are key components and the main driving force
in soil nutrient cycling and energy flow. Soils with a high
functional diversity of microorganism, which occur very often
under organic agriculture practice, develop disease and insect
suppressive properties and can help to induce resistance in
plants (Fliebach et al., 2007). Since microbial biomass and its
activity plays a significant role in regulating processes of
nutrient cycling, studying the change of microbial biomass
and soil enzymes under diverse organic inputs may help us to
better understand the impact of organic amendments on
improving soil fertility.
Comparative analysis of heterotrophic bacterial counts in
organic and fertilizer fields revealed that heterotrophic count
was significantly low in fertilizer stations as compared to the
organic stations. Determination of soil microbial biomass is
generally used as a rapid indicator of change in soil
management which in turn affects the turnover of organic
matter (Nannipieri et al., 1990). A relatively rapid response to
organic amendments has been reported for microbial biomass
carbon by several workers which suggest it could be a useful
indicator in identifying positive effects of soil management
(Fauci and Dick, 1994) [36]. Axelsen and Elmholt, (1998) [4]
reported that a transition to 100% organic farming has
increased the microbial biomass by 77% as a national
average.
Collins et al. (1992) reported a greater amount of soil organic
matter and soil microbial biomass in continuous wheat than in
a wheat-fallow rotation after 58 years. Beare et al. (1994) [11]
indicated that tillage enhanced short-term CO2 evolution and
microbial biomass turnover, and accelerated organic C
oxidation to CO2 not only by improving soil aeration, but also
by increasing contact between soil and crop residues, and by
exposing aggregate-protected organic matter to microbial
attack. Witt et al. (2000) found that the replacement of dry
season rice by maize caused a reduction in soil C and N due
to a 33–41% increase
in the estimated amount of mineralized C and N during the
dry season. As a result, there was 11–12% more C
sequestration and 5–12% more N accumulation in soils
continuously cropped with rice than in the maize-rice rotation
with the greater amounts sequestered in N-fertilized
treatments. Tillage also exposes organic carbon in both the
inter- and intra-aggregate zones and that immobilized in
microbial cellular tissues to rapid oxidation (Roscoe and
Burman 2003). This is because of the improved availability of
O2 and the exposure of more decomposition surfaces, thereby
stimulating increased microbial activity (Jastrow et al., 1996).
Active microbial biomass and C mineralization were higher
under NT than under conventional tillage in the top 5 cm of
the soil profile (Alvarez and Alvarez 2000). Increased C
storage has been frequently observed in soils under
conservation tillage, particularly with NT (Zibilske et al.,
~ 2379 ~
Journal of Pharmacognosy and Phytochemistry 2002). Balota et al. (2003) showed that no-tillage increased
microbial biomass C, N, and P, and higher levels of more
labile C existed in no-tillage systems than in conventional
systems.
Li et al. (2013) showed that MBC was affected by the straw
return factor with an affecting force of 95.95% at 0–7 cm
depth and 97.83% at 7– 14 cm depth. The probable
explanation maybe that crop residue might enter the labile C
pool, provide substrate for the soil microorganisms, and
contribute to the accumulation of labile C.Panettieri et al.
(2013) revealed that TOC, β-glucosidase and, to a less extend,
dehydrogenase were useful as indicators of management
practices impact on soil quality. Additionally, dehydrogenase
and β-glucosidase were useful indicators to reflect changes in
soil total biological activity and biochemical status involved
in the carbon cycle Figure 14 (i). Ratnayake etal. (2013) [106]
revealed that microbes affect the turnover of their primary
substrates with increasing soluble carbon fractions such as
MBC and WSC, because organic matter acts as source of
nutrients and also improve greater nutrient retention. Liu et
al., (2013) [72] revealed that the average concentration of
particulate organic carbon (POC), dissolved organic carbon
(DOC) and microbial biomass carbon (MBC) in organic
manure plus inorganic fertilizer treatments (NP+S and
NP+FYM) in 0–60 cm depth were increased by 64.9–91.9%,
42.5–56.9%, and 74.7–99.4%, respectively, over the CK
treatment. Beesley et al., (2014) [13] opined that incorporation
of organic manure to the soil should substitute for lost C
which in turn should modulate the dynamics of soil C pools.
Apart from the addition of essential nutrients to the soil,
organic inputs also eradicate the problems of heavy metal
pollution to a considerable degree. Sharma et al., (2015) [112]
reported that the greatest soil quality index (1.61) was
observed with application of 25 kg nitrogen (N; compost) as
well as with application of 15 kg N (compost) + 10 kg N ha−1
(green leaf). The order of percentage contribution of key
indicators toward soil quality indices was available potassium
(K) (34%) > available phosphorus (P) (32%) > available N
(13%) > microbial biomass carbon (12%) > exchangeable
calcium (Ca) (9%) Figure 14(ii & iii). Akhilesh and Nandan,
(2016) [5] reported that the heterotrophic microbial count
showed an average highest value of 20x 106 cfu/g soils in
organic, whereas was 90x104 cfu/g soils in fertilizer applied.
Naresh et al. (2017) [86] also found that the values of MBC in
surface soil varied from 116.8 mgkg−1 in unfertilized control
plot to 424.1 mgkg−1 in integrated nutrient use of 50% RDN
as CF+50% RDN as FYM (F5) plots, respectively; while it
varied from 106.6 mgkg−1 (control) to 324.9 mgkg−1 (50%
RDN as CF+50% RDN as FYM F5) in sub-surface (5-15 cm)
soil layer. The values of MBC increased by 58.4 and 72.5%
under 75% RDN as CF+25% RDN as FYM (F3) and 50%
RDN as CF+50% RDN as FYM (F5) treatments in surface soil
over control. While, there were 14.5 and 43.4% increase of
MBC over 100% RDF as CF (F2) fertilizer, respectively. The
highest value of MBC due to integrated use of FYM and RDN
fertilizer might be due to higher turn-over of root biomass
produced under 50% RDN as CF+ 50% FYM treatment.
Fig 14(i): Projected loadings of the soil chemical and biochemical
properties MBN: microbial biomass nitrogen; MBC: microbial
biomass carbon; WSC: water soluble carbon; TOC: total organic
carbon; DHA: dehydrogenase activity; β-GLU: β-glucosidase
activity.
ii. iii
Fig 14 (ii & iii): Percentage contributions of key soil quality indicators towards soil quality indices in long term conjunctive nutrient-
management treatments under pearl millet system in Inceptisols of Agra
MBC was highest in the farmyard manure plus inorganic
fertilizer treatment in top soil, an increased MBC content after
farmyard application was also reported by (Chakraborty et al.,
2011; Marschner et al.,2003 and Liu et al., 2013) [23, 78, 80, 71].
This indicated the activation of microorganisms through
carbon source inputs consisting of organic residues. Increases
in soil organic matter are usually associated with similar
increases in microbial biomass because the SOM provides
principal substrates for the microorganisms Melero et al.
(2009) [82]. Among the investigated fertilizer treatments, straw
plus inorganic fertilizer had impact on the microbial biomass.
This effect is mainly due to the input of straw manure as an
organic carbon source. Srinivasan et al. (2012) [126] observed
that SOC protection by soil aggregates, the newly added
carbon provides physical protection and is then subjected to
chemical conversion and structural stabilization; meanwhile,
~ 2380 ~
Journal of Pharmacognosy and Phytochemistry alternation of the properties and distribution of the carbon
pool leads to both the diversification of aggregate-scale
microbial habitats and the evolution of microbial biota, along
with changes in various fertility service functions such as
functional groups and enzyme activity, which promote the
development of diverse biota and thereby stabilize ecosystem
processes. Lynch and Panting, (1980) [75] reported that eight
months after application of straw manure to a loamy arable
soil the microbial biomass was almost twice as high as
compared to a control. Also, Ocio et al. (1991) [89] have
demonstrated rapid and significant increases in microbial
biomass following straw inputs in field conditions. The MBC
was not only correlated with SOC concentration near the
surface but also at deeper depths. Though the average MBC
decreased with soil depth, the NP+FYM, NP+S and FYM
treatments resulted in significant increase in microbial
biomass C even in 60–80 cm soil layer.
Management shifts that can enhance SOC stocks and
Climate change
In general, any shift in management that increases inputs
and/or reduces losses should build SOC stocks especially in
soils that have lost significant quantities of SOC relative to
pre-clearing conditions. Given that climate and
physicochemical characteristics of a particular soil exert such
overriding controls on overall SOC dynamics, results from
one field trial under a particular set of climate and soil
conditions may not be applicable to another. There is
evidence that large-scale changes in farming practices to
cowpathy and so-called “biological” farming systems which
rely heavily on alternative soil amendments and manure
applications can decrease net GHG emissions (Stolze et al.
2000) [127] and increase SOC stocks (Wells et al., 2000) [136]
while maintaining or increasing farm profitability especially
during extreme climatic years (Lotter et al. 2003) [73]. Wells et
al. (2000) [136] found that in intensive vegetable farming, both
cowpathy and hybrid organic-best management practice
systems significantly increased SOC levels over more
traditional management systems. After 8 years SOC stocks to
15 cm were found to increase by 0.5 and 0.3 Mg C ha-1 yr-1
for cowpathy (organic) and low-input crop rotation systems,
respectively. While the conventional treatment showed no
change over the same period (Clark et al., 1998) [28].
Fig 15: Conversion of native vegetation to agriculture
Eleanor et al. (2008) reported that the adoption of no-tillage
systems, SOC stocks have shown an increase over time under
soybean cultivation (Figures 15). The effects of agriculture
expansion can also be observed by the SOC stock change
rates, where soybean shows the highest change rates among
the different land uses in the Brazilian Amazon. The increase
in soybean cultivation area associated with adoption of no-
tillage systems has led to an increase in SOC stocks. This is
illustrated in the SOC stock maps for 2000 and 2030 (Figure
16). In 1990 the agricultural expansion area was dominated by
SOC stock class of 20-40 t C ha-1. In the year 2000 some
areas started to be cultivated with soybean and finally in
2030, most of this region moved to a higher class of SOC
stock, now in the range of 40-60 t C ha-1 (Figure 17). Brown
and Lugo (1990) reported that abandoned agricultural lands
that reverted to forest accumulate carbon at rates proportional
to the initial forest biomass. Rates range from about 1.5 Mg C
ha-1 yr-1 in forests with initial biomass of < 100 Mg C ha-1 to
about 5.5 Mg C ha-1 yr-1 for forests with biomass of > 190
MgCha-1. Woomer et al. (1999) observed a rate of 6.2±1.3
Mg C ha-1 yr-1 of carbon sequestration in secondary forest re-
growth in the Brazilian Amazon. Watson et al. (2000)
suggested a range of carbon accumulation of 3.1 to 4.6 Mg C
ha-1 yr-1 for tropical regions over 40 years. Schroth et al.
(2002) reported that secondary forest on an infertile upland
soil in central Amazon accumulated carbon in above- and
belowground biomass and litter at a rate of about 4 Mg ha-1yr-1.'
Fig 16: SOC stock change rate
~ 2381 ~
Journal of Pharmacognosy and Phytochemistry
Fig 17: Estimated current and future SOC stocks in the agricultural
expansion area within the Brazilian Amazon
Chan (2001) found that 69 to 94% of changes in total SOC
stocks occurred in the particulate fraction for several diverse
management shifts. This is the SOC fraction that is most
sensitive to perturbation and could be easily lost with only
minor management or environmental change. Globally, Lal
(2004a) [65] estimated that 78 Pg of carbon have been lost due
to agricultural practices, with 26 Pg attributed to erosion and
52 Pg attributed to mineralization. If best management
practices, including reduced or no-till farming, cover crops,
nutrient management, manuring, efficient irrigation, and
setting aside marginal lands, were adopted on all agricultural
land, Lal (2004a) [65] estimates that 50-66% of historic losses
could be sequestered over the next 50 years. Globally, this
equates to 30 to 60 Pg C at a rate of 0.9 ± 0.3 Pg C yr-1 over
25 to 50 years. This sequestration rate is equivalent to
approximately 10% of current total GHG emissions due to
fossil fuel burning and land-use change (IPCC 2007) or 25 to
33% of the annual increase in atmospheric CO2 levels.
Kern and Johnson (1993) [57] concluded that the greatest
change of C occurred in the top 8 cm of soil, a lesser amount
in the 8- to 15-cm depth, and no significant amount below 15
cm. They also concluded that, unlike no-till (NT) in which
SOC had increased, no significant change in SOC was
detected in response to reduced tillage (RT). West and Post
(2002) indicated that on average, a change from CT to NT can
sequester 57 ± 14 g Cm-2yr-1, and by enhancing crop rotation
complexity it can sequester an average of 20 ± 12 g Cm-2yr-1.
Carbon sequestration rates can be expected to peak in 5–10
years with SOC reaching a new equilibrium in 15–20 years.
Liu et al. (2003) [71] showed a significant decline of total SOC
that occurred in the first 5 years of cultivation where the
average SOC loss per year was about 2300 kgha-1 for the 0–
17 cm horizon. The average annual SOC loss between 5- and
14-year cultivation was 950 kgha-1 and between 14- and 50-
year cultivation it was 290 kgha-1. These data clearly showed
a rapid reduction of SOC for the initial soil disturbance by
cultivation and a relatively gradual loss later. Compared with
organic matter in the uncultivated soil, Liu et al. (2003) [71]
also indicated that the total SOC loss (the sum of three
horizons) was 17%, 28%, and 55% in the 5-, 14- and 50-year
cultivation periods, respectively. Song et al. (2005) [121]
reported that a reduction in topsoil SOC storage at
(14.8±15.1) t/hm2, leading to a total loss of 1.7-2.0 Pg.
However, using similar approach, Wu and Cai, (2007) [138, 139]
revealed that a total topsoil SOC loss as high as 4.3 Pg.
Nevertheless, all these studies had described the SOC
reduction had happened mainly in those regions with
significant climate change and/or vulnerable ecosystems
though the estimation of the extent of SOC stock loss seemed
quite different.
Wu and Cai, (2007) [138, 139] indicated an up-rise of SOC
content between 0.05 gkg-1 and 0.29 gkg-1 under balanced or
combined inorganic and organic fertilization and a net SOC
sequestration of 0.2- 1.6 Pg during 1982-2005. Huang and
Sun, (2006) also observed that 53%-60% of croplands in SOC
enhancement, 30%-35% in decline and 4%-6% in balancing
during 1980s-2005. Hutchinson et al. (2007) revealed that the
sequestration potential for numerous management practices
and found that on average improvements to cropland resulted
in gains of 0.24 ± 0.20 Mg Cha-1yr-1 (mean ± s.d.), while
improvements to pasture lands resulted in increases of 0.44 ±
0.20 Mg Cha-1yr-1, and conversion from cropland to pasture
gained 0.82 ± 0.28 Mg C ha-1 yr-1.Smith et al. (2008) [119]
estimated that the global technical mitigation potential,
considering all greenhouse gases, from agriculture by 2030 is
5.5 to 6.0 Pg CO2-eq Yr-1 (or ~ 1.5 Pg C yr-1).
Stable organic matter and humic substances
Humic substances have been shown to contain a wide variety
of molecular components. Some typical components are:
polysaccharides; fatty acids; polypeptides; lignins; esters;
phenols;ethers; carbonyls; quinones; lipids: peroxides; various
combination of benzene, acetal, ketal, and lactol, and furan
ringed compounds; and aliphatic (carbon chains) compounds.
The oxidative degradation of some humic substances
produces aliphatic, phenolic, and benzenecarboxylic acids in
addition to n alkanes and n fatty acids. Humic Substances as
the fraction of SOM that is not composed of recognizable
biomolecules, such as carbohydrates, proteinaceous materials,
and lipids. Humic substances often represent 60 to 85% of
total SOM, with the highest values often reported for
agricultural soils with the remainder being dominated by
particulate OM which includes all plant residues.
~ 2382 ~
Journal of Pharmacognosy and Phytochemistry
Fig 18a: Diagram of interactions and negative impacts of agricultural management on soil quality
FIG. 18b: Long-term soil organic carbon level changes depending on carbon input and decomposition in agricultural ecosystems
Conant et al. (2001) [24] reported that globally, rates of C
sequestration by different types of management range from
0.11 to 3.04 Mg C ha–1 yr–1, with a mean of 0.54 Mg C ha–1yr–
1, and are highly influenced by biome type and climate. Ch.
Srinivasarao et al. (2012) [27] revealed that an annual
application of biomass C through crop residues and FYM
significantly enhanced SOC stock. A linear relationship (y =
6.340x +10.04, R2 = 0.58, P < 0.01) was observed between
SOC and the annual inputs of C as crop residues in different
treatments, indicating the latter’s influence on SOC stock
(Figure 19 i) Similarly, a significant relationship between the
crop residue C, external C, and the total C input with the total
SOC stock in the profile, indicated that the C input positively
influences SOC stock (Figure 19 ii). A significant
improvement in SOC, after 10 yr of the incorporation of a
cover crop [horsegram, Macrotyloma uniflorum (Lam.)
~ 2383 ~
Journal of Pharmacognosy and Phytochemistry Verdc.] biomass grown with off –season rainfall in a rainfed
Alfisol under semiarid tropical conditions was reported by
Venkateswarlu et al. (2007). Therefore the positive linear
relationship between the changes in SOC stock and the total
cumulative C inputs to the soils (external organics plus crop
residue) over the years (Y = 0.099X – 5.131; R2 = 0.99***, P
< 0.001) (Figure 19 iii) was highly significant and indicates
that even after 21 yr of C input, ranging from 1.13 to 5.55 Mg
C ha–1yr–1.
Fig 19(i): Crop residue C inputs influence soil organic carbon (SOC)
Fig 19(ii): cumulative C input through (a) crop residue, (b) external
C (organics) and (c) total C on total soil organic C stock
Fig 19: (iii) and the magnitude of critical C input and its influence on soil organic carbon (SOC) sequestration
Carbon balance
Cerri et al. (2004) [22] reported that in order to perform the
calculation for the carbon balance when forest is burned and
pasture established, requirements are needed concerning the
pools of carbon in the soil and in the biomass. Regarding the
fluxes, i.e. transfer of carbon between the different
compartments and the atmosphere. It is going to be shown
that although there is an eventual accumulation of C in the
soil when forest is converted to pasture, the total C balance
Figure 20 ends up with a large emission of C to the
atmosphere, indicating that clearing forest to pasture
establishment is not a good option in terms of greenhouse gas
emissions and therefore, an important contribution to
enhancing global climate change problems.
~ 2384 ~
Journal of Pharmacognosy and Phytochemistry
Fig 20: Carbon balance in the conversion of forest to pasture
Over long enough time periods, there must be an approximate
balance between inputs and losses, otherwise soils would
either be devoid of carbon or awash in the entire atmospheric
carbon pool (Richards et al., 2007) [109]. An example of the
importance of recognizing multiple pools with varying
turnover times, t, is given in Figure 21 (A). In this
hypothetical example, there is a step increase in C returns to
the soil of 2 Mg C ha-1 yr-1. Depending on the fate of this new
C, there is a 3-fold difference in the amount of new C
ultimately sequestered. If the new C remains as unprotected
particulate C (POC), only 6 Mg C ha-1 are added to the soil
with sequestration rates dropping to negligible levels after
only 10 years Figure 21 (B). If some of this POC becomes
incorporated into aggregates with decadal turnover times, then
8 Mg C ha-1 will be sequestered. If some of the POC and
aggregate-protected C becomes adsorbed to mineral surfaces
with a t of 120 yrs, then 18 Mg C ha-1 will be added to the soil
with sequestration rates >0.1 Mg C ha-1 yr-1 sustained for 30
years. An important collorary to this concept is that if the new
inputs cease Figure 21 (C), the C stocks will return to their
previous level rapidly if this new C has not become physically
protected.
Fig 21: Total new soil C (A) and sequestration rates (B) following a 2 Mg C ha-1 yr-1 increase in inputs with a cessation of the new inputs after
60 years for 3 scenarios: #1 – all new C enters and stays in soil as unprotected POC (MRT = 3 yrs); #2 – all new C enters as POC but a fraction
of the POC becomes protected within aggregates (MRT = 30 yrs); and #3 – as #2 with an additional fraction becoming stabilised by adsorption
to minerals (MRT = 120 yrs). Model structure shown in (C), with the 3 pools shown as boxes (turnover time, t, given for each pool), solid
arrows represent transfers, and wavy arrows represent losses as CO2. Steady state distribution of SOC amongst pools is ~25% as POC, ~15% as
aggregate-protected and ~60% as sorbed C. This model is mathematically very similar to Roth C and Century models, but the 3 pools are
represented by specific stabilization processes
Persson et al. 2008) [100] reported that the equilibrium SOC
levels and multiple pools lead to a second important insight
for soil C management: the state of the soil system prior to a
change in management may override any expected soil C
gains (e.g.). This is particularly true for soils that have only
been cultivated for short periods of time with significant
stocks of SOM derived from the native vegetation remaining.
The initial drop in C input rates from the native state to the
first cultivated state will likely take 50 to >100 years to be
fully expressed as losses as the more stable SOM pools adjust
to the new input levels. During this time period, a shift in
management so that more residues, but still less than the
amount prior to any cultivation, are returned to the soil may
not result in increased C levels because the soil is still losing
C as a result of the previous large drop in input rates.
However, if the soil had reached steady state with respect to
the initial management, then the new management with
increased residue returns would result in a significant gain in
SOC.
Lentz and Lehrsch, (2015) also found that the mean annual
total C input was 15.7, 10.8, and 10.4 Mg ha−1 for M,
(manure) F, (fertilizer) and NA,(no amendments)
respectively, while total C outputs for the three treatments
were similar, averaging12.2 Mg ha−1. Manure plots with a
mean net gain of 3.3 Mg C ha−1 Figure 22a&b.
~ 2385 ~
Journal of Pharmacognosy and Phytochemistry
Fig 22a: Mean annual transfers of C in Mg C ha−1 into and out of an irrigated silage corn and calcareous soil system amended with inorganic
fertilizer. The value shown in parentheses is the standard error of the mean (n = 8). DIC dissolved inorganic C; DOC, dissolved organic C; PIC,
particulate inorganic C; POC, particulate organic C.
Fig 22b: Mean annual transfers of C in Mg C ha−1 into and out of an irrigated silage corn and calcareous soil amended with stockpiled dairy
manure. The value shown in parentheses is the standard error of the mean (n = 8). DIC dissolved inorganic C; DOC, dissolved organic C; PIC,
particulate inorganic C; POC, particulate organic C.
Conclusion
It was recognized that soil organic matter levels are generally
low and are still declining except in the few instances where
appropriate management techniques have been introduced.
Conservation system (CS) proved to be highly effective in
enhancing SOC under the semi-arid conditions prevailing in
western Uttar Pradesh. CS were observed to lead to
differences in SOC beginning in the third year after a change
in management practice, followed by larger increase in
subsequent years. Long-term compost amendment
significantly increased the organic C content in soil by
increasing organic C in all aggregates, whereas the increase in
organic C in inorganic fertilizer–added soils was mainly
because of the enhancement in organic C content in macro-
aggregates and the silt + clay fraction. Low organic matter
and poor soil structure are one of the key reasons of yield
stagnation and even decline in yield of rice-wheat system of
India. Therefore, crop residue incorporation will enhance soil
organic matter and will improve soil structure. Soil organic C
is a key element in the valuation of natural resources and the
evaluation of how management affects soil quality and
ecosystem services derived from soil. A key to success will be
to consider the agronomic, ecological and environmental
constraints within a particular farm setting. The magnitude
and severity of the depletion of SOC pool are exacerbated
through decline in soil quality by accelerated erosion and
other degradation processes. Perpetual use of extractive
farming practices and mining of soil fertility also deplete the
SOC pool. Conversion to a restorative land use and adoption
of recommended agricultural management practices, which
create positive C and nutrient budgets, can enhance SOC pool
while restoring soil quality. As a living component of soil C
and N pool, microbial biomass serves as a reservoir of
nutrients and driver of nutrient cycling processes. The depth
~ 2386 ~
Journal of Pharmacognosy and Phytochemistry distribution of microbial biomass was impacted by long term
tillage, which may influence the potential nutrients supply to
crops. No till management regime which promoted
maintenance of crop residues at the soil surface may have
beneficial impacts on soil fertility through maintenance of
microbial biomass and supply of mineralizable nutrients.
Conventional tillage (CT) significantly reduces macro-
aggregates to smaller ones, thus aggregate stability was
reduced by 35% compared with conservation system (CS),
further indicating that tillage practices led to soil structural
damage. The concentrations of SOC and other nutrients are
also significantly higher under CS than CT, implying that CS
may be an ideal enhancer of soil productivity in this Inceptisol
ecosystem through improving soil structure which leads to the
protection of SOM and nutrients, and the maintenance of
higher nutrient content. The average concentration of
particulate organic carbon (POC), dissolved organic carbon
(DOC) and microbial biomass carbon (MBC) in organic
manure plus inorganic fertilizer treatments (NP+S and
NP+FYM) in 0–60 cm depth were increased by 64.9–91.9%,
42.5–56.9%, and 74.7–99.4%, respectively, over the CK
treatment.
Average SOC concentration of the control treatment was
0.54%, which increased to 0.65% in the RDF treatment and
0.82% in the RDF+FYM treatment and increased enzyme
activities, which potentially influence soil nutrients dynamics
under field condition. A regular input of biomass-C along
with chemical fertilizers is essential to improving soil quality
in the semi arid tropics of India, and for minimizing the
depletion of SOC stock under continuous cropping. Use of
organic amendments is essential to enhancing the SOC
sequestration. The minimum input of 1.1 Mg C ha−1 year−1 is
needed to maintain SOC at the initial level (with no change).
In view of the decreasing availability of FYM, however,
application of 10.7 Mg ha–1 of FYM (equivalent to 60 kg N)
on dry weight basis is difficult. Thus, conjunctive use of FYM
or other crop residues along with 50% recommended dose of
fertilizers is a viable option for curbing SOC depletion and
sustaining crop production. Hence, balanced use of NPK
fertilizer along with FYM or other crop residues, which will
take care of critical-C-input addition quantitatively, will be a
better option to stop SOC depletion and maintain and sustain
crop production.
References
1. Adesodun JK, Adeyemi EF, Oyegoke CO. Distribution of
nutrient elements within water-stable aggregates of two
tropical agro-ecological soils under different land uses.
Soil Till Res. 2007; 92:190-197.
2. Alvarez CR, Alvarez R. Short-term effects of tillage
systems on active soil microbial biomass. Biol. Fert.
Soils, 2000; 31:157-161.
3. Aswathanarayana U. (ed). Natural resources-technology,
economics and policy. CRC Press, Boca Raton, 2012.
4. Axelsen JA, Elmholt S. Jordbundens biologi. The Bichel
committee, Report from the interdisciplinary working
group on organic farming, Sub-report A3.4. (In danish),
Environmental Protection Agency, 1998, 1-112.
5. Akhilesh Vijay, Nandan BS. Soil Quality Indicators and
Microbial Development in Organic and Conventionally
Farmed Paddy Wetlands Ecosystem in Kerala –India. Int.
J. Scientific Res Pub. 2016; 6(6):112-117.
6. Balota EL, Colozzi A, Andrade DS, Dick RP. Microbial
biomass in soils under different tillage and crop rotation
systems. Biol. Fert. Soils. 2003; 38:15-20.
7. Baker JM, Ochsner TE, Venterea RT Griffis TJ. Tillage
and soil carbon sequestration-what do we really know?
2007; 118:1-5
8. Bappa Das, Debashis C, Singh VK, Aggarwal P, Singh
R, Dwivedi BS. Effect of organic inputs on strength and
stability of soil aggregates under rice-wheat rotation. Int.
Agrophys. 2014; 28:163-168.
9. Batjes NH. Carbon and nitrogen in the soils of the world.
European J Soil Sci. 1996; 47(2):151-163
10. Bäumler R, Caspari T, Totsche KU, Dorji T, Norbu C,
Baillie IC. Andic properties in soils developed from
nonvolcanic materials in central Bhutan. J Plant Nutr.
Soil Sci. 2005; 168:703-713.
11. Beare MH, Cabrera PF, Hendrix, Coleman DC.
Aggregate-protected and unprotected organic matter
pools in conventional and no-tillage soils. Soil Sci Soc
Am J. 1994; 58:787-795.
12. Beer J, Bonnemann A, Chavez W, Fassbender HW,
Imbach AC, Martel I. Modelling agroforestry systems of
cacao (Theobroma cacao) with laurel (Cordiaalliadora)
or poro (Erythrinapoeppigiana) in Costa Rica. V.
Productivity indices, organic material models and
sustainability over ten years. Agroforestry Sys. 1990;
12:229-249.
13. Beesley L, Inneh OS, Norton GJ, Moreno-Jimenez E,
Pardo T, Clemente R et al. Assessing the influence of
compost and biochar amendments on the mobility and
toxicity of metals and arsenic in a naturally contaminated
mine soil. Environ. Poll. 2014; 186:195-202.
14. Begum F, Bajracharya RM, Sharma S, Sitaula BK.
Influence of slope aspect on soil physico-chemical and
biological properties in the mid hills of central Nepal. Int.
J. Sustain. Dev. World Ecol. 2010; 17:438-443.
15. Bhardwaj DR, Abdoulie A, Sanneh, Rajput, Bhalendra
Singh, Kumar Sanjeev. Status of Soil Organic Carbon
Stocks Under Different Land Use Systems in Wet
Temperate North Western Himalaya. J. Tree Sci. 2013;
32(1, 2):14-22.
16. Bhattacharyya T, Pal DK, Velayutham M, Chandran P,
Mandal C. Organic carbon stock in Indian soils and their
geographical distribution. Curr Sci. 2000; 79(5):655-660
17. Bhattacharyya T, Pal DK, Velayutham M, Chandran P,
Mandal C. Total carbon stock in Indian soils: issues,
priorities and management. In: Land Resource
Management for food and environment security
(ICLRM). Soil Conservation Soc India, New Delhi,
2000a, 1-46.
18. Bhattacharyya R, Kundu S, Srivastava AK, Gupta HS,
Ved-Prakash RB, Bhatt JC. Long term fertilization
effects on soil organic carbon pools in a sandy loam soil
of the Indian Himalayas. Plant Soil. 2011; 341:109-124.
19. Bhattacharyya R, Tuti MD, Bisht JK, Bhatt JC, Gupta
HS. Conservation tillage and fertilization impact on soil
aggregation and carbon pools in the Indian Himalayas
under an irrigated rice-wheat rotation. Soil Sci 2012a;
177:218-228.
20. Bernoux M, da Conceic S, Carvalho M, Volkoff B, Cerri
CC. Brazil’s soil carbon stocks. Soil Sci Soc Am J. 2002;
66:888-896
21. Cambell MGR. Carbon sequestration and biomass energy
offset: theoretical, potential and achievable capacities
globally, in Europe and the UK. Biomass and Bioenergy.
2003; 24:97-116
22. Cerri CC, Bernoux M, Cerri CEP, Feller C. Carbon
cycling and sequestration opportunities in South
~ 2387 ~
Journal of Pharmacognosy and Phytochemistry America: the case of Brazil. Soil Use and Management,
2004; 20(1):248-254.
23. Chakraborty A, Chakrabarti K, Chakraborty A, Ghosh S.
Effect of long term fertilizers and manure application on
microbial biomass and microbial activity of a tropical
agricultural soil. Bio Fert Soils. 2011; 47:227-233.
24. Chan KY. Soil particulate organic carbon under different
land use and management. Soil Land Use Manag. 2001;
17:217-221.
25. Chen HYH, Shrestha BM. Stand age, fire and clear
cutting affect soil organic carbon and aggregation of
mineral soils in boreal forests. Soil Biol Biochem. 2012;
50:149-157.
26. Ch. Srinivasarao, Venkateswarlu B, Lal R, Singh AK,
Kundu S, Vittal et al. Long-Term Manuring and
Fertilizer effects on Depletion of Soil Organic Carbon
Stocks under Pearl millet- Cluster Bean- Castor Rotation
in Western India. Land Degrad. Develop. 2011; DOI:
10.1002/ldr.1158
27. Ch. Srinivasarao, Venkateswarlu B, Lal R, Singh AK,
Vittal KPR, Kundu S, Singh SR et al. Long-Term Effects
of Soil Fertility Management on Carbon Sequestration in
a Rice–Lentil Cropping System of the Indo-Gangetic
Plains. SSSAJ: 2012; 76(1):168-178.
28. Clark MS, Horwath WR, Shennan C, Scow KM. Changes
in soil chemical properties resulting from organic and
low-input farming practices. Agro. J. 1998; 90:662-671.
29. Collins HP, Rausmussen PE, Douglas CL. Jr. Crop
rotation and residue management effects on soil carbon
and microbial dynamics. Soil Sci. Soc. Am. J., 1992;
56:783-788.
30. Dalal RC, Mayer RJ. Long-term trends in fertility of soils
under continuous cultivation and cereal cropping in
southern Queensland. 2. Total organic-carbon and its rate
of loss from the soil profile. Australian J. Soil Res. 1986;
24:281-292.
31. Dhama K, Rajesh Rathore, Chauhan RS, Tomar S.
Panchgavya (Cowpathy): An overview. Internat J Cow
Sci. 2005; 1(1):1-15
32. Dumanski J, Lal R. THEME PAPER: Soil Conservation
and the Kyoto Protocol Facts and Figures. Agriculture
and the Environment, Environment Bureau, Agriculture
and Agri-Food Canada, Ottawa, ONTARIO, 2004.
33. Egli M, Sartori G, Mirabella A, Favilli F, Giaccai D,
Delbos E. Effect of north and south exposure on organic
matter in high alpine soils. Geoderma. 2009; 149:124-
136.
34. Eleanor Milne, Mark Easter, Carlos Eduardo Cerri, Keith
Paustian, Steve Williams. Assessment of Soil Organic
Carbon Stocks and Change at National Scale. Technical
Report of GEF Co-Financed Project No. GFL-2740-02-
4381, 2006, 1-168.
35. Fang C, Smith P, Moncrieff JB, Smith JU. Similar
response of labile and resistant soil organic matter pools
to changes in temperature. Nature. 2005; 433:57-59.
36. Fauci MF, Dick RP. Soil microbial dynamics: short-term
and long-term effects of inorganic and organic nitrogen.
Soil Sci Soc Am J. 1994; 58:801-806.
37. Feng YS, Li XM. An analytical model of soil organic
carbon dynamics based on a simple “hockey stick”
function. Soil Sci. 2001; 166:431-440.
38. Fliebach A, Oberholzer HR, Gunst L, Madar P. Soil
organic matter and biological soil quality indicators after
21 years of organic and conventional farming, Agric,
Ecosyst Enviro. 2007; 118:273-284.
39. Food & Agriculture Organization (FAO). Soil Carbon
Sequestration for Improved Land Management. World
Soil Resources Reports, 2001, No. 96, ISSN 0532-0488.
Rome, Italy, 2001
40. Forster P, Ramaswamy V, Artaxo P, Berntsen T, Betts R,
Fahey DW et al. Changes in atmospheric constituents and
in radioactive forcing. In: Climate change (2007). The
physical science basis, Chapter 2, 2007.
41. Freibauer A, Rounsevell MDA, Smith P, Verhagen J.
Carbon sequestration in the agricultural soils of Europe.
Geoderma, 2004; 122:1-23.
42. Ghimire R, Adhikari KR, Chen ZS, Shah SC, Dahal KR.
Soil organic carbon sequestration as affected by tillage,
crop residue, and nitrogen application in rice-wheat
rotation system. Paddy Water Environ. 2012; 10:95-102.
43. Gathala MK, Ladha JK, Saharawat YS, Kumar V, Kumar
V, Sharma PK. Effect of tillage and crop establishment
methods on physical properties of a medium-textured soil
under a seven-year rice–wheat rotation. Soil Sci Soc Am
J, 2011b; 75:1851-1862.
44. Hansen J, Kharecha P, Sato M, Masson-Delmotte V,
Ackerman F, Beerling DJ. et al. Assessing “Dangerous
Climate Change”: Required reduction of carbon
emissions to protect young people, future generations and
nature (JA, Ed.), PLoS ONE. 2013; 8(12):e81648.
45. Hossain M. Nutrient and residue management for
improving productivity and N use efficiency of rice-
wheat-mungbean systems in Bangladesh. In: The
Proceedings of the International Plant Nutrition
Colloquium XVI. Uinversity of California, Davis, CA,
USA, 2009.
46. Huang Y, Sun WJ. Tendency of SOC change in cropland
soils of China over the last 20 years. Chinese Sci Bull,
2006; 51(15):1785-1803
47. Hungate BA, Elisabeth A, Holland, Robert, Jackson B,
Stuart Chapin III,F., Harold A. M. and Christopher, B.
Field. The fate of carbon in grasslands under carbon
dioxide enrichment. Nature. 1997; 388:576-579.
48. Hutchinson JJ, Campbell CA, Desjardins RL. Some
perspectives on carbon sequestration in agriculture. Agri.
Forest Meteorology. 2007; 142:288-302.
49. IPCC. Climate change 2014 synthesis report. Fifth
assessment report. 2014. http://ar5-syr.ipcc.ch/. Accessed
26 Jan 2016
50. Jastrow JD, Boutton TW, Miller RM. Carbon dynamics
of aggregate-associated organic matter estimated by
carbon-13 natural abundance. Soil Sci. Soc. Am. J. 1996;
60:801-807.
51. Jha M, Chourasia S, Sinha S. Microbial consortium for
sustainable rice production. Agroecology and Sustainable
Food Systems. 2013; 37:340-362.
52. Jobbágy EG, Jackson RB. The vertical distribution of soil
organic carbon and its relation to climate and vegetation.
Ecol. Appl. 2000; 10:423-436.
53. Jonathan Sanderman, Ryan Farquharson, Jeffrey
Baldock. Soil Carbon Sequestration Potential: A review
for Australian agriculture. Department of Climate Change
and Energy Efficiency. CSIRO Land and Water, 2009.
54. Kamp P, Purohit D, Mandal M, Rout KK. Nutrient
management for carbon sequestration and sustainable
crop production under tropical rice- rice agro ecosystem.
Academy of Management. 2017; 5:117-129
55. Kell DB. Breeding crop plants with deep roots: their role
in sustainable carbon, nutrient and water sequestration,
Annals Bot. 2011; 108(3):407-418.
~ 2388 ~
Journal of Pharmacognosy and Phytochemistry 56. Kell DB. Large-scale sequestration of atmospheric
carbon via plant roots in natural and agricultural
ecosystems: Why and how, Philosophical Transactions of
the Royal Soc. B Bio Sci. 2012; 367:1589-1597.
57. Kern JS, Johnson MG. Conservation tillage impacts on
national soil and atmospheric carbon levels. Soil Sci. Soc.
Am. J. 1993; 57:200-210.
58. Koul DN, Shukla G, Panwar P, Chakravarty S. Status of
soil carbon sequestration under different land use systems
in Terai Zone of West Bengal, Environment & We: An
Int. J Sci. Tech. 2011; 6:95-100.
59. Kukal SS, Rasool R, Benbi DK. Soil organic carbon
sequestration in relation to organic and inorganic
fertilization in rice-wheat and maize-wheat systems. Soil
Till. Res. 2009; 102:87-92.
60. Kumar BM, George SJ, Suresh TK. Fodder grass
productivity and soil fertility changes fewer than four
grass + tree associations in Kerala, India. Agroforestry
Sys. 2001; 52:91-106.
61. Lal R, Kimble J, Follett RL. use on soil C pools in
terrestrial ecosystem. In: R. lal, J. Kimble, R.F.Fallett and
B.A. Steward (Eds). Management of carbon sequestration
in soil. CRC/Lewis Publishers, Boca Raton, F. L.
62. Lal R. Soil management and restoration for C
sequestration to mitigate the accelerated greenhouse
effect. Progress in Environmental Sci. 1999; 1:307J326
63. Lal R. Global potential of soil carbon sequestration to
mitigate the greenhouse effect. Crit Rev Plant Sci. 2003;
22:151-184
64. Lal R. Soil carbon sequestration in India. Climatic
Change. 2004; 65:277J296
65. Lal R. Soil carbon sequestration impacts on global
climate change and food security. Sci, 2004a; 304:1623-
1627.
66. Lal R. Carbon sequestration. Philosophical Transactions
of the Royal Society. 2008; B363:815-830
67. Ladha JK, Reddy CK, Padre AT, van Kessel C. Role of
nitrogen fertilization in sustaining organic matter in
cultivated soils. J Environ Quality. 2011; 40:1756-1766
68. Leifeld J, Fuhrer J. Organic farming and soil carbon
sequestration: What do we really know about the
benefits? Ambio. 2010; 39:585-599
69. Lentz RD, Lehrsch GA. Manure and Fertilizer Effects on
Carbon Balance and Organic and Inorganic Carbon
Losses for an Irrigated Corn Field. Soil Sci Soc Am J.
2014; 78(3):987-1002
70. Li CF, Yue LX, Kou ZK, Zhang ZS, Wang JP, Cao CG.
Short-term effects of conservation management practices
on soil labile organic carbon fractions under a rape–rice
rotation in central China. Soil Till, Res. 2012; 119:31-37.
71. Liu XB, Han XZ, Herbert SJ, Xing B. Dynamics of soil
organic carbon under different agricultural management
systems in the black soil of China. Commun. Soil Sci.
Plant Anal. 2003; 34:973-984.
72. Liu E, Yan C, Mei X, Zhang Y, Fan T. Long-Term Effect
of Manure and Fertilizer on Soil Organic Carbon Pools in
Dry-land Farming in Northwest China. PLoS ONE. 2013;
8(2):e56536. doi:10.1371/journal.pone.0056536
73. Lotter DW, Seidel R, Liebhardt W. The performance of
organic and conventional cropping systems in an extreme
climate year. Am. J Alternative Agri. 2003; 18:146-154.
74. Lu F, Wang XK, Han B, Ouyang ZY, Duan XN, Zheng
HUA et al. Soil carbon sequestrations by nitrogen
fertilizer application, straw return and no-tillage in
China’s cropland. Global Change Biol. 2009; 15:281-
305.
75. Lynch JM, Panting LM. Variations in the size of the soil
biomass. Soil Biol Biochem. 1980; 12:547-550.
76. Madari B, Machado PLOA, Torres E, de Andrade AG,
Valencia LIO. No tillage and crop rotation effects on soil
aggregation and organic carbon in a Rhodic Ferralsol
from southern Brazil. Soil Till Res. 2005; 80:185-200.
77. Majumder B, Mandal B, Bandyopadhyay PK,
Gangopadhyay A, Mani PK, Kundu AL et al. Organic
amendments influence soil organic carbon pools and rice-
wheat productivity. Soil Sci Soc Am J. 2008; 72:775-785.
78. Mamta Kumari, Chakraborty D, Gathala MK, Pathak H,
Dwivedi BS, Tomar RK et al. Soil Aggregation and
Associated Organic Carbon Fractions as Affected by
Tillage in a Rice–Wheat Rotation in North India. Soil
Bio. Biochem. 2011; 75:560-567
79. Mandal B, Majumder B, Bandyopadhyay PK, Hazra GC,
Gangopadhyay A, Samantaray RN et al. The potential of
cropping systems and soil amendments for carbon
sequestration in soils under long-term experiments in
subtropical India. Global Change Biol. 2007; 13:357-369.
80. Marschner P, Kandeler E, Marschner B. Structure and
function of the soil microbial community in a long-term
fertilizer experiment. Biol Fertility Soils. 2003; 35:453-
461.
81. Mazumdar SP, Kundu DK, Nayak AK, Ghosh Debjani.
Soil Aggregation and Associated Organic Carbon as
Affected by Long Term Application of Fertilizer and
Organic Manures under Rice-Wheat System in Middle
Gangetic Plains of India. J Agri Phy. 2015; 1(2):113-121.
82. Melero S, Lo´pez-Garrido R, Murillo JM, Moreno F.
Conservation tillage: Short-and long-term effects on soil
carbon fractions and enzymatic activities under
Mediterranean conditions. Soil Till Res. 2009; 104:292-
298.
83. Moshin F, Singh RP, Singh K. Nutrient cycling of poplar
plantation in relation to stand age in agroforestry system.
Indian Journal of Agroforestry. 1996; 19:302-310.
84. Naresh RK, Gupta Raj K, Gajendra Pal, Dhaliwal SS,
Kumar Dipender, Kumar Vineet. et al. Tillage Crop
Establishment Strategies and Soil Fertility Management:
Resource Use Efficiencies and Soil Carbon Sequestration
in a Rice-Wheat Cropping System. Eco. Env. & Cons.
2015; 21:121-128.
85. Naresh RK, Gupta Raj K, Jat ML, Singh SP, Dwivedi
Ashish, Dhaliwal SS et al. Tillage, irrigation levels and
rice straw mulches effects on wheat productivity, soil
aggregates and soil organic carbon dynamics after rice in
sandy loam soils of subtropical climatic conditions. J.
PURE APPL MICROBIO, 2016; 10(3):1987-2002
86. Naresh RK, Gupta RK, Minhas PS, Rathore RS, Dwivedi
Ashish, Kumar Mukesh et al. Toward Optimal Soil
Organic Carbon Sequestration with effects of
Agricultural Management Practices and Climate Change
in Upland Soils of Subtropical India: A Review. Int.J.
Chem. Stu. 2017; 5(2):433-442.
87. Nayak AK, Gangwar B, Shukla AK, Mazumdar SP,
Anjani K, Rajab R, Kumar V et al. Long-term effect of
different integrated nutrient management on soil organic
carbon and its fractions and sustainability of rice–wheat
system in Indo Gangetic Plains of India. Field Crops Res.
2012; 127:129-139.
88. Niggli U, Fließbach A, Hepperly P, Scialabba N. Low
Greenhouse Gas Agriculture: Mitigation and Adaptation
~ 2389 ~
Journal of Pharmacognosy and Phytochemistry Potential of Sustainable Farming Systems (Food and
Agriculture Organization of the United Nations, Rome),
2009.
89. Ocio JA, Martinez J, Brookes PC. Contribution of straw-
derived N to total microbial biomass N following
incorporation of cereal straw to soil. Soil Biol Biochem.
1991; 23:655-659.
90. Ontl TA, Schulte A. Soil "C" storage, Nature Education
Knowledge, 2012; 3(10):35.
91. Onweremadu EU, Onyia VN, Anikwe MAN. Carbon and
nitrogen distribution in water- stable aggregates under
two tillage techniques in Fluvisols of Owerri area,
southeastern Nigeria. Soil Till Res. 2007; 97:195-206.
92. Onwudike SU. Effectiveness of cow dung and mineral
fertilizer on soil properties, nutrient uptake and yield of
sweet potato (Ipomoea batatas) in Southeastern Nigeria.
Asian J Agric Res. 2010; 4:148-154.
93. Panettieri M, Carmona I, Melero SE, Madejón E, Gómez-
Macpherson H. Effect of permanent bed planting
combined with controlled traffic on soil chemical and
biochemical properties in irrigated semi-arid
Mediterranean conditions. Catena. 2013; 107:103-109.
94. Pandey D, Agrawal M, Singh, Bohra J, Adhya TK,
Bhattacharyya P. Recalcitrant and labile carbon pools in a
sub-humid tropical soil under different tillage
combinations: A case study of rice-wheat system. Soil
Till Res. 2014; 143:116-122.
95. Parker MA, Nyakatawa EZ, Reddy KC, Reeves DW. Soil
carbon and nitrogen as influenced by tillage and poultry
litter in North Alabama. In: E. van Santen (ed.) Making
Conservation Tillage Conventional: Building a Future on
25 years of Research, Proceedings of the 25th Annual
Southern Conservation Tillage Conference for
Sustainable Agriculture, Auburn AL, 2002, 283-287.
96. Pathak H, Jain N, Bhatia A, Patel J, Pramod K. Global
warming mitigation potential of biogas plants in India.
Environ. Monit. Assess. 2009; 157:407-418.
97. Pathak H, Byjesh K, Chakrabarti B, Aggarwal PK.
Potential and cost of carbon sequestration in Indian
agriculture: Estimates from long-term field experiments.
Field Crops Res. 2011; 120:102-111
98. Paudel M, Sah SK, Andrew McDonald, Chaudhary NK.
Soil Organic Carbon Sequestration in Rice-Wheat
System under Conservation and Conventional
Agriculture in Western Chitwan, Nepal. World J Agri Res
2014; 2:(6A):1-5
99. Paustian K, Parton WJ, Persson J. Modeling soil organic
matter in organic amended and nitrogen fertilizer long-
term plots. Soil Sci. Soc. Am. J. 1992; 56:476-488.
100. Persson T, Bergkvist G, Katterer T. Long-term effects of
crop rotations with and without perennial leys on soil
carbon stocks and grain yields of winter wheat. Nutrient
Cycling Agroecosystems. 2008; 81:193-202.
101. Pimentel D, Harvey C, Resosudarmo P, Sinclair K, Kurz
D, McNair M et al. Environmental and economic costs of
soil erosion and conservation benefits. Science. 1995;
267:1117-1123.
102. Poeplau C, Don A. Sensitivity of soil organic carbon
stocks and fractions to different land-use changes across
Europe. Geoderma. 2013; 192:189-201
103. Post WM, Kwon KC. Soil carbon sequestration and land-
use change: processes and potential, Global Change
Biology. 2006; 6:317-327.
104. Rahangdale CP, Pathak NN. Dynamics of Organic
Carbon Stock in Soil under Agroforestry System. Trends
in Biosciences. 2016; 9(11):662-667.
105. Ramesh P, Rao AS. Organic farming: Status and
Research achievements. Indian Institute of Soil Science
Bhopal, 2009, 74.
106. Ratnayake RR, Seneviratne G, Kulasooriya SA. Effect of
soil carbohydrates on nutrient availability in natural
forests and cultivated lands in Sri Lanka. Eurasian Soil
Sci. 2013; 46:579-586.
107. Razafimbelo TM, Albrecht A, Oliver R, Chevallier T,
Chapuis-Lardy L, Feller C. Aggregate associated-C and
physical protection in a tropical clayey soil under
Malagasy conventional and no-tillage systems. Soil Till
Res. 2008; 98:140-149.
108. Rao KT, Rao AU, Reddy DS. Dynamics of soil fertility
in organic farming studies of maize -sunflower – green
gram cropping system. Internat. J Plant Sci. 2013;
8(1):35-41.
109. Richards AE, Dalal RC, Schmidt S. Soil carbon turnover
and sequestration in native subtropical tree plantations.
Soil Bio Biochem. 2007; 39:2078-2090.
110. Roscoe R, Burman P. Tillage effects on soil organic
matter in the density fractions of a Cerrado Oxisol. Soil
Till. Res. 2003; 70:107-119.
111. Sapkota TB, Jat RK, Singh RG, Jat ML, Stiring CM, Jat
MK et al. Soil organic carbon changes after seven years
of conservation agriculture in a rice–wheat system of the
eastern Indo-Gangetic Plains. Soil Use Manag. 2017;
33:81-89.
112. Sharma KL, Sharma SC, Bawa SS, Sher Singh,
Chandrika DS, Grace JK et al. Effects of Conjunctive
Nutrient Management on Soil Fertility and Overall Soil
Quality Index in Submountainous Inceptisol Soils under
Rainfed Maize (Zea mays L.)–Wheat (Triticum aestivum)
System. Commu. Soil Sci. Plant Anal. 2015; 46:47-61.
113. Silveira ML, Comerford NB, Reddy KR, Cooper WT, El-
Rifai H. Characterization of soil organic carbon pools by
acid hydrolysis. Geoderma. 2008; 144:405-414.
114. Singh G, Jalota SK, Singh Y. Manuring and residue
management effects on physical properties of a soil under
the rice–wheat system in Punjab. Soil Till. Res. 2007;
94:229-238.
115. Sisti CPJ, Santos HP, Kohhann R, Alves BJR, Urquiaga
S, Boddey RM. Change in carbon and nitrogen stocks in
soil less than 13 years of conventional or zero tillage in
southern Brazil. Soil Till Res. 2004; 76:39-58.
116. Smith P, Andren O, Karlsson T, Perala P, Regina K,
Rounsevell M, Van Wesemael B. Carbon sequestration
potential in European croplands has been overestimated.
Global Change Biology. 2005; 11:2153-2163.
117. Smith P. Carbon sequestration in croplands: the potential
in Europe and the global context. Europe Agro. 2004;
20:229-236
118. Smith P, Andren O, Karlsson T, Perala P, Regina K,
Rounsevell M et al. Carbon sequestration potential in
European croplands has been overestimated. Global
Change Biolology. 2005; 11:2153-2163
119. Smith, P, Martino D, Cai Z. Greenhouse gas mitigation in
agriculture. Philos Trans R Soc Lond B Biol Sci. 2008;
363:789-813.
120. Sombrero A, de Benito A. Carbon accumulation in soil.
Ten-year study of conservation tillage and crop rotation
in a semi-arid area of Castile-Leon, Spain. Soil Till Res.
2010; 107:64-70
~ 2390 ~
Journal of Pharmacognosy and Phytochemistry 121. Song Guohan, Pan Genxing, Zhang Qi. Topsoil SOC
storage of China agricultural soils and its loss by
cultivation. Biogeochemistry. 2005; 74:47-62
122. Song Ke, Jianjun Yang, Yong Xue, Weiguang Lv,
Xianqing Zheng, Jianjun Pan. Influence of tillage
practices and straw incorporation on soil aggregates,
organic carbon, and crop yields in a rice-wheat rotation
system. Scientific Reports | 6:36602 | DOI:
10.1038/srep36602, 2016.
123. Sperow M, Eve M, Paustian K. Potential soil C
sequestration on US agricultural soils. Climatic Change.
2003; 57:1573-1580
124. Srivastava P, Singh PK, Singh R, Bhadouria R, Singh
DK, Singh S et al. Relative availability of inorganic N-
pools shifts under land use change: an unexplored
variable in soil carbon dynamics. Ecol Ind. 2016a;
64:228-236.
125. Srivastava P, Singh R, Tripathi S, Raghubanshi AS. An
urgent need for sustainable thinking in agriculture—an
Indian scenario. Ecol Ind. 2016b; 67:611-622.
126. Srinivasan V, Maheswarappa HP, Lal R. Long term
effects of topsoil depth and amendments on particulate
and non particulate carbon fractions in a Miamian soil of
Central Ohio. Soil Till Res. 2012; 121:10-17.
127. Stolze M, Piorr A, Haring A, Dabbert S. Environmental
impacts of organic farming in Europe In 'Organic
Farming in Europe: Economics and Policy'. (Department
of Farm Economics, University of Hohenheim, Germany.
Stuttgart-Hohenheim), 2000.
128. Swamy SL, Puri S, Singh AK. Growth, biomass, carbon
storage and nutrient distribution in Gmelina arborea
Roxb. Stands on red lateritic soils in central India.
Bioresource Technology. 2003; 90:109-126
129. Trumbore SE. Potential responses of soil organic carbon
to global environmental change. Proc Nat Acad Sci.
1997; 94:8284-8291
130. USEPA U.S. National Climate Assessment, 2014.
http://nca2014. globalchange.gov/. Accessed 26 Jan 2016
131. US Climate Change Sci Program. The First State of the
Carbon Cycle Report (SOCCR): Agricultural and
Grazing Lands, 2007.
132. Vaccari FP, Lugato E, Gioli B, Acqui DL, Genesio L,
Toscano P, Matese A et al. Land use change and soil
organic carbon dynamics in Mediterranean agro-
ecosystems: the case study of Pianosa Island. Geoderma
2012; 175:29-36.
133. Venkanna K, Mandal UK, Solomon Raju AJ, Sharma
KL, Ravikant V, Adake Pushpanjali et al. Carbon stocks
in major soil types and land-use systems in semiarid
tropical region of southern India. Curr. Sci. 2014;
106(4):604-611
134. Vitousek PM, Sanford RL Jr. Nutrient cycling in moist
tropical forest. Annual Review of Ecological System.
1986; 17:137-167.
135. West TO, Post WM. Soil organic carbon sequestration
rates by tillage and crop rotation: A global data analysis.
Soil Sci. Soc. Am. J. 2002; 66:1930-1946.
136. Wells AT, Chan KY, Cornish PS. Comparison of
conventional and alternative vegetable farming systems
on the properties of a yellow earth in New South Wales.
Agri Ecosys Environ. 2000; 80:47-60.
137. Witt C, Cassman KG, Olk DC, Biker U, Liboon SP,
Samson MI et al. Crop rotation and residue management
effects on carbon sequestration, nitrogen cycling and
productivity of irrigated rice system. Plant Soil. 2000;
225:263-278.
138. Wu LZ, Cai ZC. Effect of agricultural cultivation on soil
organic carbon in China. J Soil Water Conser. 2007;
21(6):118-121
139. Wu LZ, Cai ZC. Estimation of the change of topsoil
organic carbon of croplands in China based on long-term
experimental data. Eco. Environ. 2007; 16(6):1768-1774.
140. Wu J. Long-term fertilizer effects on organic carbon and
total nitrogen and coupling relationships of C and N in
paddy soils in subtropical China. Soil Till Res. 2009;
106:8-14.
141. Xu XW. Distribution and Variation of Soil Organic
Carbon Storage in Agricultural Soils at Different Spatial
Scale. Nanjing: Nanjing Agricultural University, 2008
142. Zibilske LM, Bradford JM, Smart JR. Conservation
tillage induced changes in organic carbon, total nitrogen
and available phosphorus in a semi-arid alkaline
subtropical soil. Soil Till. Res., 2002; 66:153-163.
143. Zhou H, Peng X, Perfect E, Xiao T, Peng G. Effects of
organic and inorganic fertilization on soil aggregation in
an ultisol as characterized by synchrotron based X-ray
micro-computed tomography. Geoderma. 2013; 195-
196:23-30.