Soil organic carbon: Towards better soil health

3 downloads 0 Views 835KB Size Report
On the other hand, labile organic C is the soil nutrient reservoir and is closely related with diversified soil biology. For the sustainable and holistic soil resource management .... intensive cultivation resulted exponential decline of SOC.
Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34 DOI: 10.5958/2320-642X.2015.00003.4

REVIEW ARTICLE

Soil organic carbon: Towards better soil health, productivity and climate change mitigation

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

Shovik Deb1* • Pratap Bhanu Singh Bhadoria2 • Biswapati Mandal3 • Amitava Rakshit4

Abstract The presence of organic C in soil is a key determinant for soil quality and productivity. Soil, being the largest C sinks, also controls the global warming. In this regard, this review focused onto the soil C dynamics, C sequestration potential of soil and related C pools. Detailed discussion of several researches depicted that, C sequestration depends onto soil C saturation deficit, presence of biochemically protected recalcitrant C fractions, aggregation and aggregate associated physically shielded C. On the other hand, labile organic C is the soil nutrient reservoir and is closely related with diversified soil biology. For the sustainable and holistic soil resource management and to mitigate climate change, this study also highlighted the possible management practices towards longer residence time of C in soil. Keywords Soil organic C, C sequestration, Pools of soil C, Management practices, Soil quality, Environmental sustainability, Climate change. Abbreviations C: carbon; OC: organic C; SOC: soil organic C; LTFE: long-term fertility experiments; SOM: soil organic matter; Ctot: soil total organic C; Cinorg: soil inorganic C; Cmic: microbial biomass C; Cmin: mineralizable C; qCO2: soil metabolic or respiratory quotient; MQ: microbial quotient 1. Introduction The global carbon (C) cycle is one of the most important biogeochemical cycles. Soils are the largest global C sink (Montagnini and Nair, 2004), harboring approximately twothirds of the C in ecosystems (Schimel et al., 1994). Soil stores approximately 615 Gt C in top 0.2 m and 2,344 Gt C up to 3 m depths, which is more than the summation of



Harikesh Bahadur Singh5

biomass and atmospheric C pool (Fontaine et al., 2007). Dynamics of soil organic C (SOC) is gaining increasing importance for its impact onto climate change and crop production. Soil organic C has the slowest turnover rates in terrestrial ecosystems (Trumbore, 1997) and thus C sequestration in soils has the potential to mitigate CO2 loading in the atmosphere (Paustian et al., 1997). On the other hand, SOC is one of the most important components in soil that positively contributes to soil fertility, tilth and crop production (Bauer and Black, 1994; Lal, 2004). Soil physical environment is controlled by the presence of SOC as it favourably affects soil porosity, aggregation and soil water storage (Benbi et al., 1998; Chenu et al., 2000). Organic C (OC) also exerts a significant influence onto chemical properties of soils (Rowsell et al., 2004; Singh et al., 2010), nutrient availability (Benbi and Biswas, 1997; Nieder and Richter, 2000), cation exchange capacity (van Dijk, 1966) and retention and mobilization of metal ions (Stevenson, 1986). Furthermore, OC serves as the energy and food source for soil microbes (Reeves, 1997). Therefore, soil as a C tank is a matter of prime concern (Lal, 2004; Xiong et al., 2014). This is more important particularly for tropical and sub-tropical regions of the world, where soils are intrinsically low in OC stock. Figure 1 depicted the present-day worldwide distribution of SOC. The worldwide expansion of agriculture in the last decades has been accompanied by a rapid oxidation of OC from soils while burning of fossil fuels from industries and automobiles results elevated levels of atmospheric CO2 (four times of the pre-industrial level) (Vellinga and Wood, 2008). Considering the importance of SOC to maintain soil quality, productivity in a long run and to mitigate global warming and climate change, this review focused onto the C

Assistant Professor, Department of Soil Science and Agricultural Chemistry, Uttar Banga Krishi Viswavidyalaya, Pundibari 736 165, West Bengal, India Professor, Department of Agricultural and Food Engineering, Indian Institute of Technology, Kharagpur 721302, West Bengal, India 3 Professor, Directorate of Research, Bidhan Chandra Krishi Viswavidyalaya, Kalyani 741 235, West Bengal, India 4 Assistant Professor, Department of Soil Science & Agricultural Chemistry, 5Professor, Department of Mycology & Plant Pathology, Institute of Agricultural Science, Banaras Hindu University, Varanasi 221 005, Uttar Pradesh, India; *Corresponding author e-mail id: [email protected] 1 2

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34

27

Figure 1 World map of soil organic C: Topsoil (30 m) Source: Food and Agriculture Organization, United Nations (http://www.fao.org/nr/land/sols/en/)

sequestration potential of soil, soil C pools and proper management practices which lead towards a holistic pathway to maintain an overall sustainable soil environment. 2. Methodology Extensive literature review was done with the help of the academic search engine scholar.google.com. Further, Thomson Reuters Web of Knowledge (http://wokinfo.com) was used to gather necessary information. Hardcopy research articles, books, monographs, and project reports were also used to collect as many as possible required database onto SOC sequestration, dynamics, budgeting, stock, saturation, pools, impact of soil C onto soil health and climate and management of soil C. The following sections of this article discussed about all these aspects in detail. 3. Soil C sequestration Carbon sequestration can be defined as the arrest and storage of C in soil that would else be emitted to or remained in the atmosphere. On the other hand, C saturation implies that, soil cannot store any additional C inputs after it reaches the maximum C stabilization capacity (Paustian et al., 1997; Six et al., 2002). Therefore, determining the relative C status of a soil in comparison to its C saturation capacity is

important to understand the C sequestration potential of that very soil. A soil is rendered as either a source or sink of the atmospheric CO2 by agricultural practices (Piao et al., 2010). However, before soil can be credited as a sink of atmospheric CO2, there are needs to understand the C sequestration process in the soil and develop appropriate methodology for determining how much and for how long C is sequestered in the soil. This means the methods must be able to measure the specific proportion of SOC (or the specific SOC pools) involved in C sequestration before they are useful for global C budgeting purposes. Long-term fertility experiments (LTFE) are the primary source of information to find out the consequences of soil management, cropping systems and other anthropogenic activities onto the quantitative and mechanistic changes in SOC pools (Grace et al., 2006). The LTFEs in both Europe and North America pointed out that intensive cultivation resulted exponential decline of SOC (Robert et al., 2001; Ogle et al., 2003; Shi et al., 2010). In Indian context, Katyal et al. (2001) had proven that treatment and practice that supported soil organic matter (SOM) buildup, also favoured sustainable productivity in 30 years old LTFE in tropical soil. Long-term comparative studies inferred that organic and sustainable systems resulted buildup

28

Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

Figure 2 Different pools/ fractions of soil organic C and their relationship with different components of ecology

of SOM and thus improved soils sustainability (Kong et al., 2005; Lal, 2006; Manna et al., 2006; Rudrappa et al., 2006). Observed rates of C sequestration range from 0-150 kg C ha -1 y -1 in humid and cool in dry and warm regions (Armstrong et al, 2003) and 100 to 1000 kg C ha-1 y-1 in humid and cool climate (Sá et al., 2001). In comparison, the sequestration rate of inorganic C (Cinorg) as secondary carbonates is low in soil. However, to understand the soil C sequestration it is indeed important to understand the pools of soil C. 4. Pools of soil C 4.1 Soil organic C Quantitative data on SOC pools and fluxes at scales ranging from pedon or soil-scape to ecosystem and regional, national and global scales, are needed to assess the magnitude of soil C dynamics in relation to the biotic and atmospheric C pool and to evaluate the contribution of the soil C pool to the atmospheric pool (Chan, 1997). As per Majumder et al. (2008a), the SOC stock is comprised of active or labile pool and stable and passive or recalcitrant pool (Figure 2). This active or labile pool of SOC is one of the most important components contributing in soil health, sustainability and crop production (Lal, 2004; Bationo et al., 2007; Ghosh et al., 2012) as well as the food and energy source for soil micro-organisms (Steenwerth et al., 2002). The most labile SOC components are considered sensitive indicators of change in the soil quality (Maia et al., 2007). On the other hand, stable, passive or recalcitrant pool of SOC is biochemically protected (Parton et al., 1987), altered very slowly by microbial activities (Weil et al., 2003). These pools are comprised of a range of resistant and non resistant

aromatic and long chain aliphatic compounds. Labile SOC contains microbial biomass and is closely associated with nutrient mineralization and reflects organic input management over the past years (Barrios et al., 1996). Dissolved organic matter also represents a tiny and very labile C pool (Ellert and Gregorich, 1995). 4.2 C pools related to soil micro-organisms Micro-organisms are essential for all soil biological functions, formation of soil aggregates and they are indispensable for nutrient availability for plants (SalinasGarcia et al., 1997; Stenberg, 1999). The microbial biomass denotes the living component of SOM (Jenkinson and Ladd, 1981). Microbial biomass in soil is composed of bacteria, fungi, algae, actinomycetes, protozoa and some nematodes. Soil microbial biomass serve as: (i) a labile source or an immediate sink of available nutrients and organic substrates on a short term basis, (ii) a driving force of nutrient transformation from stable organic forms to available mineral form over longer periods, (iii) an agent of polysaccharide secretion, a cementing agent of soil aggregates (Kennedy and Papendick, 1995) and (iv) an agent for releasing and containing enzymes which are responsible for nutrient cycling (Srivastava and Singh, 1991). In soil, microbial biomass C (Cmic) and mineralizable C (Cmin) are the pools most commonly used as the representative of biomass and activity (in terms of respiration) of soil microorganisms. Soil Cmic (expressed as mg g-1 soil) comprises 1 to 5% of SOC (w/ w). The soil Cmic is used as a sensitive indicator of changes in soil environment (Paul, 1984). Usually there is a prominent correlation between SOC and soil microbial biomass (Biederbeck et al., 1984). Thus management practices that increase incorporation of organic

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34

residues naturally boost biological activity. On the other hand, soil respiration (CO2–C release) and soil Cmin is an index that reflects the total activity or energy spent by the soil microbial pool (Anderson and Domsch, 1990). This soil CO 2 –C emission depends on several parameters like substrate variability, soil moisture and temperature (Sparling, 1997). Therefore, Cmin is one of the most important parameter to monitor the microbial mediated processes like decomposition of organic matter in soil. Rate of soil respiration depends on the substrate availability, moisture and temperature of the soil (Brookes, 1995). In soils of tropical and subtropical regions, higher SOM turnover rate resulted in higher amount of C min within a short span (Rudrappa et al., 2006; Majumder et al., 2008b; Mandal et al., 2007). Soil metabolic or respiratory quotient (qCO2) (i.e. soil respiration to microbial biomass ratio), widely used to evaluate soil ecosystem, is a very clear-cut soil microbial index (Bastida et al., 2008). Soil microbial quotient (MQ) i.e. percentage of soil total organic C (Ctot) present as Cmic or Cmic: C toc ratio is also used as an indicator of changing soil process. These indices are more useful measure than either Cmic or Ctoc (Anderson and Domsch, 1990; Sparling, 1992) because these are ratios and therefore avoid the problems of working with absolute values and help in evaluating soils with different organic matter content. 4.3 Soil inorganic C In soil, the Cinorg (lithogenic and pedogenic inorganic C) is present mainly in form of calcium carbonate (Mikhailova and Post, 2006). In terms of soil quality, productivity and health, this fraction of soil C is less important than SOC but sequestration of Cinorg in soil plays a considerable role to mitigate global warming. Although the amount and vertical distribution of Cinorg depends on climate, land use and land cover type (Wu et al., 2009), Lettens et al. (2004) found that, the Cinorg values are significantly related to the soil geological characteristics and increase linearly with soil depth. The soil Cinorg has a positive correlation with mean annual temperature and negative correlation with mean annual precipitation. The content of Cinorg generally follows the order: desert, grassland> shrubland, cropland> marsh, forest, meadow (Mi et al., 2008). However, the largest difference between Cinorg stocks has been observed between the continuously cropped field and native grassland. Mikhailova and Post (2006) has found that in the top 2 m soil layer, native grassland contained 107 Mg ha-1 Cinorg; while cut hay field, continuously cropped field and continuous fallow (for 50 years) possessed 91, 242 and 196 Mg ha-1 Cinorg respectively. On the other hand, researches revealed, heavy grazing activities affects Cinorg more than the SOC (Reeder et al., 2004). In analytical viewpoint, the Cinorg

29

measurement is necessary to obtain the correct SOC values from combustion method (Sherrod et al., 2002). 4.4 Soil aggregate associated C Aggregation is a soil physical phenomenon of significance which has prominent impact onto soil structure, water balance, aeration, temperature, crop growth, biological activity and soil erosion (Grandy and Robertson, 2006). As terrestrial C sequestration partly is achieved through SOC stabilization by physical occlusion within aggregates, protected from mineralization (Six et al., 2000; Shrestha et al., 2007), judicious soil management considering soil aggregate formation is an important strategy towards C sequestration in soil (Bronick and Lal, 2005; Shrestha et al., 2007). As per hierarchical model, in soil, persistent, transient, and temporary SOM are associated with > 0.25 mm macro-aggregates, 0.05-0.25 mm micro-aggregates, and < 0.05 mm silt and clay, respectively which distinctly indicated that decomposability of SOM decreases with decreasing particle size owing to physical protection (Tisdall and Oades, 1982; Balesdent et al., 2000). According to this model, transient forms of SOM could act as binding agent causing micro-aggregates (0.5-0.25 mm) to form stable macro-aggregates (> 0.25 mm) (Olchin et al., 2008). Increased SOM input can lead to increased aggregate formation (Kong et al., 2005) which in turn enhances C sequestration by physical protection of SOM inside aggregates. The quality and amount of SOC associated with soil aggregates and particles vary with the size of these structural units. It is often observed that C in micro-aggregates is older and less labile than C macro-aggregates (Jastrow, 1996). Microbial derived C is believed to bind micro-aggregates into macro-aggregates (Tisdall and Oades, 1982). Studies indicated that the macro-aggregate structure exerts some physical protection to SOM (Beare et al., 1994), whereas SOM is mostly protected in free micro-aggregates (Six et al., 1998; Lichter et al., 2008) and in micro-aggregates within the macro-aggregates (Denef et al., 2001; Bossuyt et al., 2002; Lichter et al., 2008). 5. Management of soil C for sustainable development Several natural as well as anthropogenic factors influence C stock and pool in soil (Liang et al., 2007) (Figure 3). Among these, impact of climate and soil properties onto soil C stock and dynamics are of beyond control (Senapati et al., 2014). However, practices like suitable cropping system and proper land use is the pathway for soil C management. In this part of the review, influence of natural factors i.e. climate and soil properties on soil C dynamics has been highlighted first followed by a detail discussion about the impact of cropping system and land use onto soil C.

30

Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

Figure 3 Factors affecting organic C stock, pools and dynamics in soils

6. Impact of climate and soil properties on soil C dynamics

7. Land use, cropping system and soil C management

Temperature and precipitation (climate) are the most significant factors controlling SOC (Alvarez and Lavado, 1998). Climatic conditions with high precipitation, low temperature and frozen soil in winter favour the high accumulation of organic matter in soil. These conditions slower the breakdown of added SOM through plant residues, roots and hence the C sequestration in soil may be expected to be larger than warmer and drier climates (Desjardins et al., 1991). On the other hand, the potential for C sequestration with crop rotations is greater in the sub-humid than in drier climates and it is established that tropical soil contains the least C in a stable pool (Tiessen et al., 1998). Again, the C sequestration potential of soil is greater in humid temperate areas in comparison to semi-arid and tropical areas (Pretty and Ball, 2001). It is the high annual temperature which consequences the lowest average SOC stock in Indian soils among the Asian countries (Kyuma, 1988). On the other hand, according to Campbell et al. (1996), a linear correlation exists between soil texture and the SOC. Furthermore, the distribution of OC within different soil structural units controls the average residence time of C in soil (Oades, 1998). Organic C content of soil increases with decreasing particle size (Guggenberger et al., 1994). As per Saggar et al. (1996), in general, more than the half of the total SOC is associated with the clay fraction (< 0.002 mm), probably due to the protection effect of clay on SOC mineralization. The degree of protection provided by clay appears to be also dependent onto the type of clays, e.g. higher porous (e.g. allophane) and expanding (eg. montmorillonite) clay minerals offering more protection than kaolinite (Franzluebbers and Arshad, 1996; Zech et al., 1997). This association of organic matter with soil fractions is further related to mean annual temperature. As researches inferred, the average turnover time of silt-associated SOM is highest in temperate soils whereas SOM attached to clay particles is considered as the most recalcitrant fraction in tropical climate (Christensen, 1992).

Changes in land use are extensively identified as a potential driver for the shift into global C dynamics (Houghton et al., 1999). Nature of land cover namely forest, pasture, plantation, fallow or annual agricultural crops has significant influences on the C stock as well as the content of different pools of C in soils (Grace et al., 2006; Kurganova et al., 2010; Banger et al., 2010). Reconstructions of global land use in past few centuries have contributed noteworthy augmentation in CO2 emissions into the atmosphere (Post et al., 1990). Forestry is known as an important land use system for C sequestration in soils. Afforestation results in a considerable amount of new soil C sequestration as well as increases the residence time of already existing C in soil providing physical protection and stabilization in SOM associated with soil aggregates (Galdo et al., 2003). Grasslands have also been revealed as a potential C sink by recent studies (Sampson et al., 2000; Conant et al., 2001) as presence of greater root biomass and higher return ratio of residues resulted higher SOM contents (Lal, 2002). When these natural systems are put into agricultural use, major changes occur in both the C pool size and turnover rates. Mandal et al. (2007) have shown that because of cultivation there is a significant decline in native C content in soils. The magnitude of decline also varies depending upon the nature and intensity of cropping. Crop rotation can modify microbial C dynamics, which determine the SOC sequestration potential (Balota et al., 2004). Field operations like surface mulching, no-tillage and minimum tillage are also important, especially in tropical soils, as they reduces the soil surface temperature resulting less C mineralization (Lal, 1989). Cropping systems also have a prominent mark onto the soil C stock and pools. A number of researchers (Studdert and Echeverria, 2000; Halvorson et al., 2002) reported that cropping system or crop rotation with or without fallow period in LTFE affected the size and distribution of SOC pools. Decline in the fallow practices (Rasmussen et

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34

al., 1980), addition of legumes and cover crops (Kuo et al., 1997) and balanced use of manures and fertilizers (Hartwig and Ammon, 2002) results increase into SOC stock. Legumebased cropping systems have a positive impact to reduce C and N losses. As per Majumder et al. (2008a, b), inclusion of legume in cropping sequence (e.g. rice-barseem) check the loss of applied C significantly vis-à-vis other sequences (e.g. rice-wheat-fallow, rice-wheat-jute) where no such legumes were included. Cultivation of perennial forages in rotation also increases SOM levels (Nilsson, 1986). Most of the results presented above are related to ‘upland crops’ grown under aerobic conditions. However, the SOC cycles in lowland paddy systems vary distinctly from any of the upland crop systems, since it remains under submergence for a certain period of time. Transformation of C in soils under submergence is different from well aerobic soils and therefore, C sequestration and dynamics of its different pools are expected to be different. This was reflected by more SOC in stable fractions under lowland rice-rice ecology due to slow decomposition of organic substances under prolong water-logging (Mandal et al., 2008). 8. Conclusion There is a growing need to look into the detailed dynamics of C stock in soils and the role of soil in harbouring the atmospheric C and its sequestration in a long run. Any attempt to enrich soil C reservoir through increasing its residence time will help to manage global warming and reach towards global food security (Bruce et al., 1999). For a sustainable future, a proper balance should always be maintained between C inputs into soil and exports which create the equilibrium and thus determine the potential for soil to serve as a C sink. References Alvarez R and Lavado RS (1998). Climate, organic matter and clay content relationships in the Pampa and Chaco soils, Argentina. Geoderma, 83: 127–141. Anderson TH and Domsch KH (1990). Application of ecophysiological quotients (qCO2 and qD) on microbial biomasses from soils of different cropping histories. Soil. Biol. Biochem., 22: 251–255. Armstrong RD, Millar G, Halpin NV, Reid DJ and Standley J (2003) Using zero tillage, fertilisers and legume rotations to maintain productivity and soil fertility in opportunity cropping systems on a shallow Vertosol. Aust. J. Exp. Agr. 43: 141-153. Balesdent J, Chenu C and Balabane M (2000). Relationship of soil organic matter dynamics to physical protection and tillage. Soil Till. Res., 53: 215–230. Balota EL, Filho AC, Andrade DS and Dick RP (2004). Long-term tillage and crop rotation effects on microbial biomass and C and N mineralization in a Brazilian Oxisol. Soil Till. Res., 77: 137– 145. Banger K, Toor GS, Biswas A, Sidhu SS and Sudhir K (2010). Soil organic carbon fractions after 16-years of applications of

31

fertilizers and organic manure in a Typic Rhodalfs in semi-arid tropics. Nutr. Cycl. Agroecosyst., 86: 391–399. Barrios E, Buresh RJ and Sprent JI (1996). Organic matter in the soil particle size and density fractions from maize and legume cropping systems. Soil Biol. Biochem., 28: 185–193. Bastida F, Zsolnay A, Hernández T and García C (2008). Past, present and future of soil quality indices: a biological perspective. Geoderma, 147: 159–171. Bationo A, Kihara J, Vanlauwe B, Waswa B and Kimetu J (2007). Soil organic carbon dynamics, functions and management in West African agro-ecosystems. Agric. Syst., 94: 13–25. Bauer A and Black AL (1994). Quantification of the effect of soil organic matter content on soil productivity. Soil Sci. Soc. Am. J., 58: 185–193. Beare MH, Hendrix PF and Coleman DC (1994). Water-stable aggregates and organic matter fractions in conventional- and notillage soils. Soil Sci. Soc. Am. J., 58: 777–786. Benbi DK and Biswas CR (1997). Nitrogen balance and N recovery after 22 years of maize–wheat–cowpea cropping in a long-term experiment. Nutr. Cycl. Agroecosyst., 47: 107–114. Benbi DK, Biswas CR, Bawa SS and Kumar K (1998). Influence of farmyard manure, inorganic fertilizers and weed control practices on some soil physical properties in a long-term experiment. Soil Use Manage., 14: 52–54. Bhadoria PBS, Prakash YS, Kar S and Rakshit A (2003) Relative Efficacy of organic manures on the performance of rice in a lateritic soil. Soil Use Manage.19: 80-82. Biederbeck VO, Campbell CA and Zentner RP (1984). Effect of crop rotation and fertilization on some biological properties of a loam in southwestern Saskatchewan. Can. J. Soil Sci., 64: 355–367. Bossuyt H, Six J and Hendrix PF (2002). Aggregate protected C in no-tillage and conventional tillage agroecosystems using carbon14 labeled plant residue. Soil Sci. Soc. Am. J., 66: 1965–1973. Bronick CJ and Lal R (2005). Soil structure and management: a review. Geoderma, 124: 3–22. Brookes PC (1995). The use of microbial parameters in monitoring soil pollution by heavy metals. Biol. Fert. Soils., 19: 269–279. Bruce JP, Frome M, Haites E, Jazen H, Lal R and Paustian K (1999). Carbon sequestration in soils. J. Soil Water Conserv., 54: 382– 389. Campbell CA, McConkey BG, Zentner RP, Selles F and Curtin D (1996). Long-term effects of tillage and crop rotations on soil organic C and total N in a clay soil in southwestern Saskatchewan. Can. J. Soil Sci., 76: 395–401. Chan KY (1997). Consequences of changes in particulate organic carbon in vertisols under pasture and cropping. Soil Sci. Soc. Am. J., 61: 1376–1382. Chenu C, Le Bissonnais Y and Arrouays D (2000). Organic matter influence on clay wettability and soil aggregate stability. Soil Sci. Soc. Am. J., 64: 1479–1486. Christensen BT (1992). Physical fractionation of soil and organic matter in primary particle size and density separates. In: Stewart BA (ed.), Advances in Soil Science, vol. 20, Springer-Verlag, New York, NY, pp. 1–90. Conant RT, Paustian K and Elliott ET (2001). Grassland management and conversion into grassland: effects on soil carbon. Ecol. Appl., 11: 343–355. Denef K, Six J, Paustian K and Merckx R (2001). Importance of macroaggregate dynamics in controlling soil carbon stabilization: short-term effects of physical disturbance induced by dry–wet cycles. Soil Biol. Biochem., 33: 2145–2153. Desjardins Th, Volkoff B, Andreaux F and Cerri C (1991). Distribution du carbon total et de l’isotope13C dans des sols ferrallitiqyes du Bresil. Science du Sol, 29: 175–187.

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

32

Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34

Ellert BH and Gregorich EG (1995). Management-induced changes in the actively cycling fractions of soil organic matter. In: McFee WW and Kelly JM (eds.), Carbon Forms and Functions in Forest Soils. Soil Sci. Soc. Am., Madison, WI, pp. 119–138. Fontaine S, Barot S, Barre P, Bdioui N, Mary B and Rumpel C (2007). Stability of organic carbon in deep soil layers controlled by fresh carbon supply. Nature, 450: 277–281. Franzluebbers AJ and Arshad MA (1996). Soil organic matter pools during early adoption of conservation tillage in north western Canada. Soil Sci. Soc. Am. J., 60: 1422–1427. Galdo ID, Six J, Peressotti A and Cotrufo MF (2003). Assessing the impact of land-use change on soil C sequestration in agricultural soils by means of organic matter fractionation and stable C isotopes. Glob. Change Biol., 9: 1204–1213. Ghosh S, Wilson B, Ghoshal S, Senapati N and Mandal B (2012). Organic amendments influence soil quality and carbon sequestration in the Indo-Gangetic plains of India. Agric. Ecosyst. Environ., 156: 134–141. Grace PR, Ladd JN, Robertson GP and Gage SH (2006). SOCRATES—a simple model for predicting long-term changes in soil organic carbon in terrestrial ecosystems. Soil Biol. Biochem., 38: 1172–1176. Grandy SA and Robertson GP (2006). Aggregation and organic matter protection following tillage of a previously uncultivated soil. Soil Sci. Soc. Am. J., 70: 1398–1406. Guggenberger G, Christensen BT and Zech W (1994). Land-use effects on the composition of organic matter in particle-size separates of soil: I. Lignin and carbohydrate signature. Eur. J. Soil Sci., 45: 449–458. Halvorson AD, Wienhold BJ and Black AL (2002). Tillage, nitrogen, and cropping system effects on soil carbon sequestration. Soil Sci. Soc. Am. J., 66: 906–912. Hartwig NL and Ammon HU (2002). Cover crops and living mulches. Weed Sci., 50: 688–699. Houghton RA, Hackler JL and Lawrence KT (1999). The US carbon budget: contributions from land-use change. Science, 285: 574– 578. Jastrow JD (1996). Soil aggregate formation and the accrual of particulate and mineral-associated organic matter. Soil Biol. Biochem., 28: 665–676. Jenkinson DS and Ladd JN (1981). Microbial biomass in soil: measurement and turnover. In: Paul EA and Ladd JN (eds.), Soil biochemistry, vol. 5, Marcel Dekker, Inc., New York and Basel, pp. 415–471. Katyal JC, Rao NH and Reddy MN (2001). Critical aspect of organic matter management in the Tropics: the example of India. Nutr. Cycl. Agroecosyst., 61: 77–88. Kennedy AC and Papendick RI (1995). Microbial characteristics of soil quality. J. Soil Water Conserv., 5–6: 243–248. Kong AYY, Six J, Bryant DC, Denison RF and van Kessel C (2005). The relationship between carbon input, aggregation, and soil organic carbon stabilization in sustainable cropping systems. Soil Sci. Soc. Am. J., 69: 1078–1085. Kuo S, Sainju UM and Jellum EJ (1997). Winter cover crops effects on soil organic carbon and carbohydrate in soil. Soil Sci. Soc. Am. J., 61: 145–152. Kurganova IN, Lopes de Gerenyu VO Shvidenko AZ and Sapozhnikov PM (2010). Changes in the organic carbon pool of abandoned soils in Russia (1990–2004). Eur. Soil Sci., 43: 333–340. Kyuma K (1988). Paddy soils of Japan in comparison with those in tropical Asia. In: Proceedings, First International Symposium on Paddy Soil Fertility. Chiangmai, Thailand, pp. 5–19. Lal R (1989). Conservation tillage for sustainable agriculture: tropics vs. temperate environments. Adv. Agron., 42: 85–197.

Lal R (2002). Soil carbon dynamics in cropland and rangeland. Environ. Pollut., 116: 353–362. Lal R (2004). Soil carbon sequestration impacts on global climate change and food security. Science, 304: 1623–1627. Lal R (2006). Enhancing crop yields in the developing countries through restoration of the soil organic carbon pool in agricultural lands. Land Degrad. Dev., 17: 197–209. Lettens S, Van Orshoven J, van Wesemael B and Muys B (2004). Soil organic and inorganic carbon contents of landscape units in Belgium derived using data from 1950 to 1970. Soil Use Manage., 20: 40–47. Liang AZ, Zhang XP, Fang HJ, Yang XM and Drury CF (2007). Shortterm effects of tillage practices on organic carbon in clay loam soil of northeast China. Pedosphere, 17: 619–623. Lichter K, Govaerts B, Six J, Sayre KD, Deckers J and Dendooven L (2008). Aggregation and C and N contents of soils organic matter fractions in a permanent raised-bed planting system in the highlands of central Mexico. Plant Soil, 305: 237–252. Maia SMF, Xavier FAS, Oliveira TS, Mendonc’a ES and Arauìjo Filho JA (2007). Organic carbon pools in a Luvisol under agroforestry and conventional farming systems in the semi-arid region of Cearaì, Brazil. Agroforest. Syst., 71: 127–138. Majumder B, Mandal B and Bandyopadhyay PK (2008b). Soil organic carbon pools and productivity in relation to nutrient management in a 20-year-old rice–berseem agroecosystem. Biol. Fert. Soils, 44: 451–461. Majumder B, Mandal B, Bandyopadhyay PK, Gangopadhyay A, Mani PK, Kundu AL and Mazumdar D (2008a). Organic amendments influence soil organic carbon pools and crop productivity in a 19 years old rice–wheat agroecosystem. Soil Sci. Soc. Am. J., 72: 775–785. Mandal B, Majumder B, Adhya TK, Bandyopadhyay PK, Gangopadhyay A, Sarkar D, Kundu MC, Guptachoudhury S, Hazra GC, Kundu S, Samantaray RN and Misra AK (2008). Potential of double-cropped rice ecology to conserve organic carbon under subtropical climate. Glob. Change Biol., 14: 2139– 2151. Mandal B, Majumder B, Bandyopadhyay PK, Hazra GC, Gangopadhyay A, Samantaray RN, Mishra AK, Chaudhury J, Saha MN and Kundu S (2007). The potential of cropping systems and soil amendments for carbon sequestration in soils under longterm experiments in subtropical India. Glob. Change Biol., 13: 357–369. Manna MC, Swarup A, Wanjari RH, Singh YV, Ghosh PK, Singh KN, Tripathi AK and Saha MN (2006). Soil organic matter in a West Bengal inceptisol after 30 years of multiple cropping and fertilization. Soil Sci. Soc. Am. J., 70: 121–129. Mi N, Wang S, Liu J, Yu G, Zhang W and Jobbágy E (2008). Soil inorganic carbon storage pattern in China. Glob. Change Biol., 10: 2380–2387. Mikhailova EA and Post CJ (2006). Effects of land use on soil inorganic carbon stocks in the Russian Chernozem. J. Environ. Qual., 35: 1384–1388. Montagnini F and Nair PKR (2004). Carbon sequestration: an underexploited environmental benefit of agroforestry systems. Agrofor. Syst., 61: 281–295. Nieder R and Richter J (2000). C and N accumulation in arable soils of West Germany and its influence on the environment— developments 1970 to 1998. J. Plant Nutr. Soil Sci., 163: 65–72. Nilsson LG (1986). Data of yield and soil analysis in the long-term soil fertility experiments. J. R. Swed. Acad. Agric. For., 18: 32– 70. Oades JM (1988). The retention of organic matter in soils. Biogeochemistry, 5: 35–80.

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34 Ogle SM, Breidt FJ, Eve MD and Paustian K (2003). Uncertainty in estimating land use and management impacts on soil organic carbon storage for US agricultural lands between 1982 and 1997. Glob. Change Biol., 9: 1521–1542. Olchin GP, Ogle S, Frey SD, Filley TR, Paustian K and Six J (2008). Residue carbon stabilization in soil aggregates of no-tillage management of dryland cropping systems. Soil Sci. Soc. Am. J., 72: 507–513. Parton WJ, Schimel DS, Cole CV and Ojima DS (1987). Analysis of factors controlling soil organic matter levels in Great Plains grasslands. Soil Sci. Soc. Am. J., 51: 1173–1179. Paul EA (1984). Dynamics of organic matter in soils. Plant Soil, 76: 275–285. Paustian K, Andrén O, Janzen H, Lal R, Smith P, Tian G, Tiessen H, van Noordwijk M and Woomer P (1997). Agricultural soil as a C sink to offset CO2 emissions. Soil Use Manage., 13: 230–244. Piao S, Fang J, Ciais P, Peylin P, Huang Y, Sitch S and Wang T (2010). The carbon balance of terrestrial ecosystems in China. Nature, 458: 1009–1013. Post WM, Peng TH, Emanuel WR, King AW, Dale VH and DeAngelis DL (1990). The global carbon cycle. Am. Sci., 78: 310–326. Pretty J and Ball A (2001). Centre for Environment and Society Occasional Paper. University of Essex, UK. Rasmussen PE, Allmaras RR, Rohde CR and Roager NC (1980). Crop residue influence on soil carbon and nitrogen in a wheat–fallow system. Soil Sci. Soc. Am. J., 44: 596–600. Reeder JD, Schuman GE, Morgan JA and Lecain DR (2004). Response of organic and inorganic carbon and nitrogen to long-term grazing of the shortgrass steppe. Environ. Manage., 33: 485–495. Reeves DW (1997). The role of soil organic matter in maintaining soil quality in continuous cropping systems. Soil Till. Res., 43: 131– 167. Robert M, Antoine J and Nachtergaele F (2001). Carbon sequestration in soils. Proposals for Land Management in Arid Areas of the Tropics. AGLL, FAO, Rome. Rowsell JLC, Millward AR, Park KS and Yaghi OM (2004). Hydrogen sorption in functionalized metal-organic frameworks. J. Am. Chem. Soc., 126: 5666–5667. Rudrappa L, Purakayestha TJ, Singh D and Bhadraray S (2006). Longterm manuring and fertilization effects on soil organic carbon pools in a typic haplustep of semi-arid sub tropical India. Soil Till. Res., 88: 180–192. Sá JC de M, Cerri CC, Dick WA, Lal R, Filho SPV, Piccolo MC and Feigl BE (2001). Organic matter dynamics and carbon sequestration rates for a tillage chronosequence in a Brazilian oxisol. Soil Sci. Soc. Am. J., 65: 1486–1499. Saggar S, Parshotam A, Sparling GP, Feltham CW and Hart PBS (1996). 14C-labeled ryegrass turnover and residence times in soils varying in clay content and mineralogy. Soil Biol. Biochem., 28: 1677–1686. Salinas-Garcia JR, Hons FM, Matocha JE and Zuberer DA (1997). Soil carbon and nitrogen dynamics as affected by long-term tillage and nitrogen fertilization. Biol. Fert. Soils, 25: 182–188. Sampson RN, Scholes RJ, Cerri C, Erda L, Hall DO, Handa M, Hill P, Howden M, Janzen H, Kimble J, Lal R, Marland G, Minami K, Paustian K, Read P, Sanchez PA, Scoppa C, Solberg B, Trossero MA, Trumbore S, Van Cleemput O, Whitmore A, Xu D, Burrows B, Conant R, Liping G, Hall W, Kaegi W, Reyenga P, Roulet N, Skog KE, Smith GR and Wang Y (2000). Additional humaninduced activities. In: Watson RT et al. (eds.), Land Use, Landuse Change, and Forestry. Cambridge University Press, Cambridge, pp. 28–180.

33

Schimel DS, Braswell BH, Holland EA, McKeown R, Ojima DS, Painter TH, Parton WJ and Townsend AR (1994). Climatic, edaphic, and biotic controls over storage and turnover of carbon in soils. Global Biogeochem. Cycles, 8: 279–293. Senapati N, Ghosh S, Daniel H and Rakshit A (2014) A basic concept on modeling soil organic carbon. In Basu SK and Kumar N (eds) Modeling and Simulation of Diffusive Processes: Methods and Applications. Springer-Verlag, London, pp. 293-313. Sherrod LA, Dunn G, Peterson GA and Kolberg RL (2002). Inorganic carbon analysis by modified pressure–calcimeter method. Soil Sci. Soc. Am. J., 66: 299–305. Shi XM, Li XG, Long RJ, Singh BP, Li ZT and Li FM (2010). Dynamics of soil organic carbon and nitrogen associated with physically separated fractions in a grassland-cultivation sequence in the Qinghai–Tibetan plateau. Biol. Fert. Soils, 46: 103–111. Shrestha BM, Singh BR, Situala BK, Lal R and Bajracharya RM (2007). Soil aggregate and particle-associated organic carbon under different land uses in Nepal. Soil Sci. Soc. Am. J., 71: 1194– 1203. Singh BP, Hatton BJ, Singh B, Cowie AL and Kathuria A (2010). Influence of biochars on nitrous oxide emission and nitrogen leaching from two contrasting soils. J. Environ. Qual., 39: 1224– 1235. Six J, Conant RT, Paul EA and Paustian K (2002). Stabilization mechanisms of soil organic matter: implications for C-saturation of soils. Plant Soil, 241: 155–176. Six J, Elliott ET and Paustian K (2000). Soil macroaggregate turnover and microaggregate formation: a mechanism for C sequestration under no-tillage agriculture. Soil Biol. Biochem., 32: 2099–2103. Six J, Elliott ET, Paustian K and Doran JK (1998). Aggregation and soil organic matter accumulation in cultivated and native grassland soils. Soil Sci. Soc. Am. J., 62: 1367–1377. Sparling GP (1992). Ratio of microbial biomass carbon to soil organic carbon as a sensitive indicator of changes in soil org-matter. Aust. J. Soil Res., 30: 195–207. Sparling GP (1997). Soil microbial biomass, activity and nutrient cycling as indicators of soil health. In: Pankhurst CE, et al. (eds.), Biological Indicators of Soil Health. CAB International, Wallingford, UK, pp. 97–119. Srivastava SC and Singh JS (1991). Microbial C, N, and P in dry tropical forest soils: effects of alternate land-uses and nutrient flux. Soil Biol. Biochem., 23: 117–124. Steenwerth KL, Jackson LE, Calderón FJ, Stromberg MR and Scow KM (2002). Soil microbial community composition and land use history in cultivated and grassland ecosystems of coastal California. Soil Biol. Biochem., 34: 1599–1611. Stenberg B (1999). Monitoring soil quality of arable land: microbial indicators. Acta Agric. Scand., B-S P 49: 1–24. Stevenson FJ (1986) Cycles of Soil Carbon, Nitrogen, Phosphorus, Sulphor, Micronutrients. John Wiley & Sons, NY. Studdert GA and Echeverria HE (2000). Crop rotations and nitrogen fertilization to manage soil organic carbon dynamics. Soil Sci. Soc. Am. J., 64: 1496–1503. Tiessen H, Cuevas E and Salcedo IH (1998). Organic matter stability and nutrient availability under temperate and tropical conditions. In: Blume HP, et al. (eds.), Towards Sustainable Land Use. Advances in GeoEcology, Catena Verlag, Reiskirchen, Germany, pp. 415–422. Tisdall JM and Oades JM (1982). Organic matter and water-stable aggregates in soils. J. Soil Sci., 33: 141–163. Trumbore SE (1997). Potential responses of soil organic carbon to global environmental change. Proc. Natl. Acad. Sci. USA, vol. 94, pp. 8284–8291.

34

Climate Change and Environmental Sustainability (April 2015) 3(1): 26-34

Downloaded From IP - 14.139.225.181 on dated 10-May-2015

www.IndianJournals.com

Members Copy, Not for Commercial Sale

Van Dijk H (1966). The Use of Isotopes in Soil Organic Matter Studies. Pergamon Press, New York, NY. Vellinga M and Wood RA (2008). Impacts of thermohaline circulation shutdown in the twenty-first century. Clim. Change, 91: 43–63. Weil RR, Islam KR, Stine MA, Gruver JB and Samson-Liebig SE (2003). Estimating active carbon for soil quality assessment: a simplified method for laboratory and field use. Am. J. Alt. Agric., 18: 3–17.Wu, H., Guo, Z., Gao, Q. and Peng, C. 2009. Distribution of soil inorganic carbon storage and its changes due to agricultural land use activity in China. Agr. Ecosyst. Environ. 129: 413-421.

Wu H, Guo Z, Gao Q and Peng C (2009). Distribution of soil inorganic carbon storage and its changes due to agricultural land use activity in China. Agric. Ecosyst. Environ., 129: 413–421. Xiong X, Grunwald S, Myers DB, Ross CW, Harris WG and Comerford NB (2014). Interaction effects of climate and land use/land cover change on soil organic carbon sequestration. Sci. Total Environ., 493: 974–982. Zech W, Senesi N, Guggenberger N, Kaiser K, Lehmann J, Miano TM, Miltner A and Schroth G (1997). Factors controlling humification and mineralization of soil organic matter in the tropics. Geoderma, 79: 117–161.