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Article

Prioritizing Tree-Based Systems for Optimizing Carbon Sink in the Indian Sub-Himalayan Region

1
Department of Forestry, Uttar Banga Krishi Vishwavidyalaya, Pundibari 736 165, India
2
Department of Forestry, Pandit Deendayal Upadhyay College of Horticulture and Forestry, Piprakothi, Rajendra Prasad Central Agricultural University, Samastipur 845 429, India
3
Department of Ecology and Environmental Science, Assam University, Silchar 788 011, India
*
Author to whom correspondence should be addressed.
Land 2023, 12(6), 1155; https://doi.org/10.3390/land12061155
Submission received: 31 January 2023 / Revised: 16 March 2023 / Accepted: 21 March 2023 / Published: 31 May 2023
(This article belongs to the Special Issue Land Use Sustainability from the Viewpoint of Carbon Emission)

Abstract

:
Land use of the sub-Himalayan region is not that intensive like the intensively land-managed region of Punjab, India. Land resources of the sub-Himalayas must be managed effectively for sustainable development by preparing carbon inventories and data banks. Such macro-level studies have not been conducted yet in the present study area, and thus were conducted to suggest sustainable land use management options. To achieve the present study’s desired goal, 33 tree-based land uses were identified from forested and agricultural landscapes of the sub-humid tropical region of West Bengal, India. Stratified random nested quadrat sampling was adopted for the study. The SOC, biomass, and carbon accumulation significantly differed. Mixed forests had the highest soil primary nutrients and carbon stock. Positive correlations were observed between SOC, total standing biomass, litter production, and ecosystem carbon. The sequence of land uses based on carbon stock was mixed-species forest > sole tree species stands in a forest landscape > tea plantations > homegardens. This baseline information can be used for developing prediction models for future interventions towards sustainable land management. The study, however, could not estimate the carbon fluxes in and out of the systems due to the absence of detailed land use land-cover databases.

1. Introduction

A land use system directly reflects anthropogenic actions into the ecosystem and bridges the economy with the biosphere, mainly through agricultural and forestry management practices [1]. Land use changes in the form of deforestation, conversion of grassland to crop and pasture, and the depletion of soil carbon through agricultural practices during the last 150 years caused one-third of all anthropogenic CO2 emissions, primarily responsible for affecting climate change [2,3,4,5,6]. Since the industrial revolution, land use change has altered a large proportion of the earth’s land surface resulting in the emission of 150 billion metric tons of carbon, which is 35% of the total anthropogenic CO2 emissions [1,7,8]. Unabated land use changes are expected to release another 10% of all CO2 during the next century [9]. Climate change is one of the present century’s significant issues responsible for reducing biological diversity and the ability of biological systems to support human needs by altering ecosystem services [10,11]. An increased concern about climate change risk has led local to global efforts for its viable mitigation through proper land management activities, which can double the carbon storage potential of the sink [12,13,14,15]. Land use and land cover change (LUCC) is critical to understand the spatial distribution, magnitude, and temporal change of terrestrial carbon sources and sinks [16,17,18], but neither has been comprehensively studied nor estimated for the Indian sub-Himalayan region.
Studies have reported the relationship between plant diversity and carbon storage [19,20,21] and the essential role of carbon sequestration by trees and soil for low-cost net emission reduction [22,23]. Soil organic matter and biomass production by vegetation and soil play an important role in the carbon cycle and are regarded as vital for their capacity to store carbon permanently and improve the local or regional and global environments [20,21,24]. In the humid tropics, the establishment of tree-based systems on degraded pastures, croplands, and grasslands would increase biomass carbon storage by 50 Mg ha−1 in 20 years, when compared to 5–15 Mg ha−1 in soils during the same period [25]. This indicates that carbon sequestration measures can considerably mitigate climate change by storing carbon in terrestrial carbon sinks like plants, plant products, and soils for a longer duration [20,21]. Thus, terrestrial carbon management is the most viable and effective strategy of the 21st century to mitigate global climate change. The tropical soils are low in organic carbon content and, in principle, have a large potential to sequester carbon through appropriate land and crop management options [26]. Therefore, biomass and soil carbon storage quantification are the most relevant in analyzing the total soil carbon sink and formulating management options at local, regional, and global levels to mitigate climate change.
The assessment of carbon storage potential has been complex due to a lack of information on biomass compartmentation and carbon allocation in different species [27,28], particularly the native species. Similarly, due to their high spatial variability, the soil carbon pool under tree-based landscapes is highly dynamic and thus difficult to analyze [29,30]. The literature survey revealed fewer comprehensive studies on land use management for climate change mitigation through tree-based land use management systems from the Terai region of West Bengal. Distribution and carbon storage changes are vital to understanding process and planning management [31,32]. Climate change and land use management studies were mainly descriptive at higher spatial scales, i.e., regional, national, and global [33,34]. There is a need to change the trend to locally convenient landscapes where land use decisions and management policies are implemented. The potential of carbon storage differs with different land use systems and their management practices because biomass production capacity and soil organic matter are the functions of site-specific interactions among edaphic, climatic, and topographic factors [35]. Hence, management strategies in one place may not apply to another. Therefore, site-specific studies on land use systems for quantifying carbon storage are essential.
Land resources have been under tremendous anthropogenic pressure due to their degradation. Land uses of the Indian sub-Himalayan region (Terai region of West Bengal) have been extensively managed and have the potential to enhance carbon sequestration, provided the land resources of this region are managed efficiently. Unlike in developed countries, carbon inventories and data banks to monitor the carbon sequestration potential of different ecosystems still need to be prepared for the Indian sub-Himalayan region. Moreover, carbon sequestration studies for diverse land uses are scarce from this region [20,21,36,37,38]. Such micro-level studies are essential for sustainable land use management for a country like India, and especially for the Terai region of West Bengal, to recommend suitable land use management prescriptions for carbon management and meeting the local and national needs. Thus, the present study was conducted to assess the suitability of different tree-based land use systems as alternatives to continuous cropping through the system’s ability to sequester and store carbon and to identify the most appropriate land use system based on carbon stock.

2. Methodology

2.1. Study Site

The study site was the Terai zone, i.e., the foothills and plains area of the Himalayas in the northern part of West Bengal, which lies between 26°30′ and 26°56′ N latitude and 88°7′ and 89°53′ E longitude (Figure 1).
The region is sub-tropical, receiving an average annual rainfall of 250–300 cm from south-west monsoons, of which 80% was received from June to August. The region has net sown area, forest area, and non-agricultural use as 56.13, 24.05, and 15.68%, respectively, of the total geographical area (bengalchamber.com/economies/west-bengal-statistics). The dominant crops are jute (Corchorus olitorius), paddy (Oryza sativa), and tobacco (Nicotiana tabacum). Plantation crops grown in the region are tea and areca nut. The area under tea cultivation is about 2000 km2 (www.jalpaiguri.gov.in, accessed on 1 March2023). A vast population in the district is directly or indirectly dependent on its forest for their livelihood.
The study area was extensively explored, and 33 tree-based land uses were identified for the present study. These land uses were categorized into five major land use systems: forest, forest tree plantations, agroforestry, commercial crop plantation, and fruit orchard. Other than forests, all other tree-based land use systems were on the agricultural landscape. The sampling details are given in Table 1. According to the landowners, the plantations in the agricultural landscape were about 15–20 years of age. Samples were collected from all the above-mentioned tree-based land use systems, and the data were presented on an average for a particular land use category. This study did not consider biomass produced by annual crops.
Agrisilvicultural systems of sole or mixed tree species, tree fruit orchards, coconut plantations, rubber plantations, and Machilus plantations are not common in the region. Except Machilus, all these plantations were planted in the Uttar Banga Krishi Viswavidyalaya campus, Pundibari for research and demonstration purposes to popularize agroforestry practices among the farmers. Machilus was planted by the State Silk Board at their experimental area for demonstration to popularize silk cultivation in the region. Machilus plantations were not found elsewhere during the survey. The sample size of these plantations was thus much smaller.

2.2. Sampling and Sample Collection

A stratified random nested quadrat sampling was adopted for collecting vegetation data. A quadrat size of 20 m × 20 m was used in the present study for trees, within which two 5 m × 5 m quadrats were laid out at the diagonal corners for shrubs, five 1 m × 1 m quadrats at the four corners, and one at the center of the 20 m × 20 m quadrat for herbs. Composite soil samples were collected once separately from 0–20, 20–40, 40–60 cm depth with the help of Dutch augur (locally prepared) from all the quadrats. Soil samples were separately collected from three different spots (separately for given depths) placed diagonally (two on the corners and one at the center). The collected samples from the different spots for the given depths were mixed to make the composite sample. In addition, litter was collected once from three 1 m × 1 m sub-quadrats placed diagonally (two at opposite corners and one in the center) within the main quadrat [39]. The litter collected was weighed in the field itself with a weighing balance.

2.3. Diameter and Height

The diameter (at breast height) and their standing height for the trees were measured with the help of a tree caliper and Ravi’s Multimeter, respectively.

2.4. Soil Physical and Chemical Parameters

The different soil physical and chemical parameters were analyzed following the method given below.
pHBeckman’s pH meter [40]
MoistureVolumetric method [41]
Bulk densityCore sampler method [41]
Electrical conductivitySoil water suspension [40]
Oxidizable organic carbon (%)Walkley and Black’s rapid titration method [40]
Available N Kg ha−1Modified Kjeldahl method [40]
Available P2O5 Kg ha−1Bray’s method [40,42]
Available K2O Kg ha−1Flame Photometer method [40]

2.5. Soil Organic Carbon Stock

The soil organic carbon stock was calculated by multiplying the organic carbon content with weight of the soil (bulk density and depth) for a particular soil depth, and was expressed as mega grams per ha (Mg ha−1).

2.6. Biomass and Biomass Carbon

An indirect or non-destructive method was adopted for biomass estimations. Tree biomass was estimated for each individual tree and then summed up:
All tree: Y = exp {−2.134 + 2.350 × In (D)}
where Y = biomass per tree, exponential function, D = diameter at breast height in cm. This equation predicts the trunk and canopy biomass of the moist (1500–4000 mm rainfall) area with reasonable precision (R2 = 0.97) and has become a standard approach [43].
The biomass of coconut palm was estimated using the equation suggested by Kumar [44]:
Y = 5.5209x + 89.355
where R2 = 0.89, Y = biomass, x = Palm age in year.
The biomass of areca palm was estimated using the equation suggested by Brown [45]:
Y = 4.5 + 7.7 H
where Y = biomass and H = stem height in meters.
The biomass of tea was estimated using equations suggested by Kalita et al. [46,47]:
AGB = 0.047 × (diameter) 1.878; BGB = 0.014 × (diameter) 1.870
Five shrubs were randomly selected from every 5 m × 5 m sub-quadrat and uprooted to measure their average fresh weight and then multiplied by the total number of shrubs in the quadrat. For herbs, all the plants from five 1 m × 1 m sub-quadrats were uprooted to measure their fresh weight. The total biomass estimated in a quadrat was converted into carbon by multiplying it with a factor of 0.50 [9]. The total of standing biomass carbon (trees + shrubs + herbs), litter carbon, and oxidizable carbon up to 60 cm soil depth was considered as the ecosystem carbon storage.

2.7. Statistical Analysis

The data were analyzed using the software package SPSS version 17.0 (VSN International, Oxford, UK) and SAS. A Pearson correlation test was performed at 0.05 (*) and 0.01 (**) probability levels. One-way variance analysis and a Duncan multiple range test (DMRT) test were also employed.

3. Results and Discussions

3.1. Soil Organic Carbon (SOC) Storage in Relation to Different Land Uses

The SOC (oxidizable) stock in different tree-based land use systems at different soil depths is given in Supplementary Table S1 and Figure 2. The tree-based land use systems and their soil depth significantly influenced SOC stock. SOC is influenced by the complex interaction of geographic location, rainfall, soil texture, and land use practices [48]. In all the tree-based land use systems, the topmost soil layer (0–20 cm) was estimated with the highest amount of SOC stock that decreased significantly with an increase in soil depth.
This trend is due to the gradual decrease of organic matter with increasing soil depth [20,21,49,50,51,52]. The range of SOC stock estimated for the entire tree-based land use systems of the Terai zone of West Bengal was 22.55–47.06 Mg ha−1, 18.15–47.13 Mg ha−1, and 16.18–32.90 Mg ha−1 at 0–20 cm, 20–40 cm, and 40–60 cm soil depth, respectively. The mixed-species forest land use was estimated with the highest amount of SOC stock at all the soil depths, which was significantly higher than all other tree-based land use systems. Overall, on an average (hectare basis), homegardens and tea plantations were estimated with 40.22% and 22.73% less SOC stock than mixed-species forest systems, respectively. On average, tree-based land use systems in forested landscapes accumulated 78.2% more SOC for a unit area than tree-based land use systems in agricultural landscapes.
Among the tree-based land use systems in the agricultural landscape, the SOC stock of forest tree plantations, agroforestry systems, commercial crop plantations, and fruit orchards was estimated with an overall average range (up to 60 cm soil depth) and overall mean of 20.0–21.53 Mg ha−1 and 20.43 Mg ha−1; 20.19–30.11 Mg ha−1 and 21.61 Mg ha−1; 20.02–34.4 Mg ha−1 and 23.39 Mg ha−1; and 19.15–20.01 Mg ha−1 and 19.53 Mg ha−1, respectively. Thus, the order of tree-based land use systems in terms of its overall mean estimated SOC accumulation in Terai zone of West Bengal is forests > commercial crop plantations > agroforestry systems > forest tree plantations > fruit orchards. Forests accumulated on an average 84%, 74%, 61%, and 91% more SOC than forest tree plantations, agroforestry systems, commercial crop plantations, and fruit orchards, respectively. In the agricultural landscape, the selected forest tree plantations were more or less statistically similar in terms of their SOC accumulation. Similarly, the different fruit orchards also accumulated statistically similar amounts of SOC. However, in agroforestry systems, homegardens were estimated with significantly higher amount of overall average SOC (up to 60 cm soil depth) than all other agroforestry systems like agri- or hortisilviculture systems (Supplementary Table S1). Similarly, among the commercial crop plantations, tea plantations accumulated a significantly higher amount of overall average SOC (up to 60 cm soil depth). Similar amounts of SOC in different land use systems were also reported by earlier studies from the Terai zone of West Bengal [20,21,48,49,50,51,52,53,54], with the highest in forest soils [53,54,55,56].
The high SOC storage in forest soil is due to the high litter addition of 13.6 Mg ha−1 (Supplementary Table S2) which regulated organic matter decomposition and the formation of a stable and liable soil organic matter pool [57,58]. On the other hand, the amount of SOC decreased with the soil depth in all the tree-based land use systems due to humus formation and the decomposition of organic matter in the upper layers. Therefore, SOC storing is vital to conserve and restrict carbon emissions. The average total SOC estimate of 113.09 Mg ha−1 in forestland up to 60 cm soil depth is similar to that reported for other tropical, moist deciduous forests in India, i.e., 8.9–176.1 Mg ha−1 for top 50 cm depth [59]. Based on major land uses, the highest mean SOC density in Indian soils under plantation systems was 253 Mg C ha−1, followed by forest (139.9 t C ha−1) and agricultural land (58.5–67.4 Mg C ha−1) [60]. The SOC storage between tree-based land uses in the Terai zone of West Bengal differed significantly. Thus, land use conversion from a higher SOC stock to a lesser one will cause significant terrestrial carbon emissions, reducing the potential for land sustainability [61]. Soil carbon sequestration through tree-based land use practices is thus an effective mitigation option to increase its carbon for agricultural productivity and sustainability and mitigate climate change [62,63]. Land use conversion from forest to agriculture can reduce more than half of the SOC stock of the system but converting to homegarden or coffee, mango, coconut, or areca nut-based agroforestry systems or a sole areca nut system on agricultural land can increase the SOC stock of the system [64].

3.2. Soil Electrical Conductivity, Moisture and pH

Soil depth and land use systems significantly influenced the soil’s electrical conductivity (EC), pH, and moisture (Supplementary Tables S3–S5 and Figure 3, Figure 4 and Figure 5). The soil depth and land use systems significantly influenced the soil electrical conductivity (EC), pH, and moisture. EC decreased significantly with increasing soil depth for all the tree-based land use systems, while the soil pH and moisture increased with the increase in soil depth. The soil under all the land use systems was acidic. Soil organic matter is mainly responsible for regulating the soil’s physical and chemical properties [65]. Generally, low pH in tree-based systems is due to higher organic matter accumulation [66] that results in high SOC with the leaching of bases and an increase in the soil EC [67]. On the other hand, higher EC and moisture of soils lower their pH [67].
The reduction in pH can be attributed to the accumulation and subsequent slow decomposition of organic matter, which releases acids [68]. This explains the more acidic nature of forest soils compared to the soils of other tree-based land use systems in which more soil organic matter is added through litter production. Forests soils, especially with mixed species, accumulated maximum soil organic matter compared to the other tree-based land use systems and thus were most acidic [20,21,51,52]. The surface layer was significantly more acidic than the sub-surface layers in all the tree-based land use systems. This is because of more organic matter in the form of litter in the top layer led to the surface soil floor’s acidic nature. The study area is humid and receives high rainfall. Humidity influences water retention directly by reducing evaporation rates and increasing water infiltration [69]. The undisturbed and continuous canopy of the forests’ stands intercepted most of the solar radiation, causing less evaporation and thereby conserving high soil moisture compared to other tree-based land use systems. Moreover, higher soil organic matter in the form of litter and humus absorbed and held substantial quantities of water, up to 20 times its mass in forest soil [70]. The continuous canopy and higher moisture retention capacity of forest soils compared to the soils of other tree-based systems help reduce the evaporation rates and water infiltration to the groundwater layers.

3.3. Soil-Available Primary Nutrients

3.3.1. Nitrogen

The soil-available nitrogen in different tree-based land use systems at different soil depths are given in Supplementary Table S6 and Figure 6. Tree-based land use systems and the soil depth significantly influenced the soil-available nitrogen. The soils of mixed-species forests were estimated with the highest available nitrogen at all the soil depths. They were significantly higher than the estimated available nitrogen of other tree-based land use systems. On an average, the mixed-species forest stored 12.79% more available nitrogen (on a hectare basis) than Shorea robusta stands, 17.03% more than Lagerstroemia parviflora stands, 17.64% more than Michelia champaca stands, and 21.81% more than Tectona grandis stands. This was 11.48% more than homegardens and 42.24% more than tea plantations. The ordering of tree-based land use system in terms of mean estimated available nitrogen in Terai zone of West Bengal is forests > fruit orchards > agroforestry systems > commercial crop plantation > forest tree plantations. Forest land use systems accumulated on an average 49.65%, 37.6%, 45.08%, and 31.27% more soil-available nitrogen than forest tree plantations, agroforestry systems, commercial crop plantations, and fruit orchards, respectively.

3.3.2. Phosphorus

The available phosphorus estimated for different tree-based land use systems at different soil depth is given in Supplementary Table S7 and Figure 7. Tree-based land use systems and the soil depth significantly influenced the soil-available phosphorus. The highest soil-available phosphorus was found in forests at all the soil depths and was significantly higher than those estimated for other tree-based systems, except the homegardens. The overall average available phosphorus (up to 60 cm soil depth) stored by tree-based land use systems in the agricultural landscape was 15.99 kg ha−1, i.e., 38.52% less than what was stored in the forests. In the agricultural landscape, tea plantations stored a significantly higher amount of available phosphorus (52.64–64.08%) than other tree-based systems. In Terai zone of West Bengal, the ordering of tree-based land use system in terms of overall soil phosphorus availability is forests > commercial crop plantations > forest tree plantations > agroforestry systems > fruit orchards.

3.3.3. Potassium

The estimated soil-available potassium of the tree-based land use systems is given in Supplementary Table S8 and Figure 8. Land use and soil depth significantly influenced the availability of potassium. The trend of the availability of potassium in the soils of the studied tree-based land use systems was similar to that of the available phosphorus. The highest amount of soil-available potassium was estimated for forests, which was significantly higher than the other tree-based land use systems. The available potassium in forest soils was 41.59% more than the agricultural landscapes. The ordering of tree-based land use system in terms of overall soil potassium availability is forests > commercial crop plantations > agroforestry systems > fruit orchards > forest tree plantations. The amount of these available primary nutrients decreased with the increase in the soil depth for all the land uses. The availability of primary soil nutrients in all the tree-based land use systems was in the order N > K > P. A similar order of these primary nutrients was also reported in earlier studies [20,21,50]. Less soil primary nutrients and organic carbon estimated for tree-based systems than forests can be attributed to the conversions of natural forests and the negative influence of such conversions that were abundantly reported across the globe [26,71].
Additionally, nitrogen, potassium, and phosphorus are differently absorbed and returned to the soil by different tree species growing in the different land use systems due to differences in the soil characteristics [72]. Variations in soil water content, aeration, temperature, microorganisms, and efficiency of the root system to absorb nutrients affect the availability of nutrients in the soil of different land use systems [73]. The availability of primary nutrients in the soil is influenced by the amount of litter produced and the nutrient content in the litter [74]. Litter produces soil organic matter, which is a source of an SOC pool, and the amount of organic matter present in the soil regulates the soil’s physical, chemical, and biological properties [65]. Pearson’s correlation matrix (Table 2) also confirmed the significant positive correlation of SOC with electrical conductivity, moisture content, and available soil primary nutrients while having a significant negative correlation with soil pH. The quality and quantity of soil organic matter (SOM) in the soil determine the availability of soil nutrients and, thus, the production potential of the soil [66,75,76]. The different tree-based land uses had a different vegetation structure, composition, and production [77], and thus also had a varied nutrient supply [78]. Soil with higher organic matter also has higher total available nitrogen, available phosphorus, and available potassium [58]. Forests have higher organic matter in their soil compared to other land use systems due to diverse vegetation with higher litter production, thus resulting in a higher amount of available nutrients in its soil [20,21,49,50,51,66]. Organic carbon and nitrogen values are lowest in barren land, intermediate in cultivated well-managed soil, and highest in forest and cultivated unmanaged land [79,80].

3.4. Biomass Accumulation and Partitioning

Standing plant biomass accumulation and partitioning in different tree-based land use systems of Terai zone of West Bengal are given in Supplementary Table S2 and Figure 9a,b. Biomass stock in the above ground and below ground parts of forests (mixed-species) were the highest with 667.49 and 100.12 Mg ha−1, respectively. High biomass storage in natural forests and stands have been reported from earlier studies [20,81]. The total biomass (trees, shrubs, herbs, and litter) of the forest (mixed-species) was highest (781.21 Mg ha−1) and was followed by the Shorea robusta stand (278.69 Mg ha−1), the Michelia champaca stand (168.84 Mg ha−1), the Tectona grandis stand (163.64 Mg ha−1), the Lagerstroemia parviflora stand (159.07 Mg ha−1), the Anthocephalus cadamba + Swietenia macrophylla plantation (111.86 Mg ha−1), homegardens (97.38 Mg ha−1), the tea plantations (77.07 Mg ha−1), and the least by the Citrus lemon orchard (6.28 Mg ha−1). In the agricultural landscape, the highest overall average total biomass was produced by forest tree plantations, agroforestry, commercial crop plantations, and the least by orchards. In all the land use systems, the major contribution was the trees (61.20–99.23%), followed by shrubs, herbs, and litter. Among the forest tree plantations, the plantation of mixed tree species accumulated significantly more biomass than other sole forest tree plantations.
The amount of biomass estimated in this study for mixed-species forests, pure tree species stands, and homegardens was comparable with earlier studies reported from the Terai zone of West Bengal [20,21,49,50,51,52,82,83]. The negligible contributions of understory vegetation to the total biomass of the tree-based land uses were also reported in these earlier studies. A similar biomass accumulation of trees and its allocation to above- and below-ground parts in forest tree plantations, commercial crop plantation, agrisilvicultural plantations, and fruit tree orchards were also abundantly reported [84,85,86,87,88]. Biomass varies with differences in land use systems along with climate, species diversity, stem density, stem size distribution, edaphic conditions, topography site quality, age, density, structure, management practices, and disturbance history, along with variations in canopy height and wood density [22,89,90]. Moreover, it would be inappropriate to draw quantitative comparisons among the studies because of significant differences in sample size, plot size, and dimensions, along with the differences in the environmental conditions and other site factors.
Biomass allocation and partitioning in different tree-based land use systems will be helpful to understand the plant life history strategies [91,92] as it influences the whole-plant net carbon gain and has a direct influence on future plant growth and reproduction [93,94]. This will improve the silvicultural techniques for efficient tree-based land use management along with identification of the productive tree-based land use systems through the productivity of tree species [95]. Biomass accumulation in tree-based land use systems can be conserved as carbon stock and cycling either regionally or globally for planning viable options to mitigate climate change. Quantifying the biomass stored in different tree-based land use systems will help to evaluate the contribution of tree species and their land use systems to net carbon emissions and their potential for carbon sequestration [96].

3.5. Biomass Carbon and Partitioning

The standing plant biomass carbon and its partitioning are significantly influenced by tree-based land use systems (Supplementary Table S9 and Figure 10a,b). The trend is exactly the same as was observed for biomass accumulation because half of the biomass is its carbon [9]. The overall average biomass carbon in the forest was significantly higher than all of the tree-based land use systems in the agricultural landscape. On an overall average, trees, shrubs, and herbs in the forest landscapes stored the highest carbon and were significantly higher than their counterparts in the other tree-based land use systems of the agricultural landscape.
Litter biomass carbon was highest in the forest as litter production was highest in it. Above-ground and below-ground biomass carbon was also highest in the forests and, therefore, the total standing live plant biomass carbon in the forest was also highest. Consequently, the overall average total, i.e., live and dead biomass carbon (155.15 Mg ha−1), was also highest in the land use systems of the forest landscapes. In the forested landscapes, the mixed-species forest accumulated the highest amount of biomass carbon 383.81 Mg ha−1, (tree 371.60 + shrub 8.90 + herb 3.31 Mg ha−1), above (333.75 Mg ha−1) and below (50.06 Mg ha−1) ground biomass carbon, litter carbon (6.8 Mg ha−1), and total carbon 390.61 Mg ha−1 (biomass + litter). The other best tree-based land use systems in terms of biomass and total carbon were sole tree species stands in forest landscapes (72.49–133.13 and 79.54–139.35 Mg ha−1, respectively) followed by the mixed-species plantation of Anthocephalus cadamba + Swietenia macrophylla (55.78 and 55.93 Mg ha−1, respectively), homegardens (47.21 and 48.69 Mg ha−1, respectively), a mixed plantation of Tectona grandis + Milvus migrans (42.12 and 42.99 Mg ha−1, respectively), a Swietenia macrophylla-based agroforestry plantation (40.41 and 41.91 Mg ha−1, respectively), tea plantations (38.41 and 38.54 Mg ha−1, respectively), and the least by the Citrus lemon orchard (3.1 and 3.14 Mg ha−1, respectively).
In terms of overall average plant biomass carbon and total carbon stock, the order of the major tree-based land use systems is forest land use (148.75 and 155.15 Mg ha−1, respectively) > forest tree plantations (26.65 and 27.82 Mg ha−1, respectively) > agroforestry plantations (19.74 and 20.14 Mg ha−1, respectively) > commercial crop plantations (18.83 and 19.09 Mg ha−1, respectively) > fruit orchards (6.22 and 6.38 Mg ha−1, respectively). Carbon stock is intricately associated with site quality, nature of land use, choice of species, and other silvicultural practices adopted [97], which explains the higher biomass of forest land uses and hence more carbon stock. Higher biomass of forest land uses was also due to efficient utilization of space due to the presence of grasses/ferns, shrubs, and trees on the same unit area of land. Higher SOC in forest soil increased the rate of plant growth, increasing the biomass again. The tree-based land uses differed in terms of diversity and tree density. It was reported that there exists a potential functional relationship between plant diversity and carbon storage [19,20,21] which is indicated through the higher carbon storage of mixed-species forests compared to other tree-based land uses. Forest land uses are plant assemblages with high species diversity with more efficient resource use and greater net primary production than with tree-based land uses with one or few species. These plant assemblages sequester carbon with higher rates than those with lower species diversity [98,99].

3.6. Ecosystem Carbon in Tree-Based Land Use Systems

Ecosystem carbon stock was significantly influenced by land use systems (Supplementary Table S10 and Figure 11a–c).
The ecosystem carbon accumulation in the tree-based land uses in both forest and agricultural landscapes was highly variable and was significantly differing among the land uses. As a consequence of the highest total standing plant biomass carbon, litter production, and total SOC of the entire observed soil depth, the forest land uses were also estimated with highest overall average ecosystem carbon stock of 268.24 Mg ha−1. The ordering of forest base land uses in terms of ecosystem carbon accumulation was mixed-species forest > the Shorea robusta stand (250.16 Mg ha−1) > the Lagerstroemia parviflora stand (193.31 Mg ha−1) > the Michelia champaca stand (190.55 Mg ha−1) > the Tectona grandis stand (189.93 Mg ha−1). Forest land uses were accumulating 3.24 times more carbon than the land uses in agricultural landscapes. The best tree-based land uses in agricultural landscapes in terms of ecosystem carbon accumulation were the tea plantations (141.74 Mg ha−1) > homegardens (139.02 Mg ha−1) > the mixed plantation of Anthocephalus cadamba + Swietenia macrophylla (116.02 Mg ha−1) > the Swietenia macrophylla-based agroforestry (104.4 Mg ha−1) > the Tectona grandis + Milvus migrans (102.99 Mg ha−1).
In terms of ecosystem carbon accumulation, the ordering of the major land uses is forests > commercial plantation crop land uses > forest tree plantations > agroforestry land uses > fruit orchards. In forest tree plantations, the best land uses in terms of ecosystem carbon were mixed plantations followed by sole tree species plantations in the order of the Anthocephalus cadamba + Swietenia macrophylla plantations (116.02 Mg ha−1) > the Tectona grandis + Milvus migrans plantations 102.99 Mg ha−1) > the Anthocephalus cadamba plantations (95.55 Mg ha−1) > the Swietenia macrophylla plantations (87.44 Mg ha−1) > the Lagerstroemia indica plantations (84.21 Mg ha−1) > the Shorea borneensis plantations (76.12 Mg ha−1) > the Gmelina arborea plantations (76.07 Mg ha−1) > the Tectona grandis plantations (74.70 Mg ha−1). The tree plantations in the agricultural landscape were between 10–15 years of age, dense and unmanaged with no silvicultural operations. This was evidenced from the growth conditions of the plantations, i.e., with less diameter and height, resulting in less biomass and carbon accumulation compared to the forest [21].
Similarly, in agroforestry land uses, the order based on ecosystem carbon accumulation was homegardens (139.02 Mg ha−1) > the Swietenia macrophylla-based (104.40 Mg ha−1) > the Anthocephalus cadamba-based (87.90 Mg ha−1) > the Gmelina arborea-based (77.31 Mg ha−1) > the Terminalia arjuna-based (73.65 Mg ha−1) > the Albizia lebbeck-based (71.14 Mg ha−1), the Lagerstroemia indica-based (71.14 Mg ha−1) > the Mangifera indica-based (71.12 Mg ha−1) > the Millettia pinnata-based (68.03 Mg ha−1). Homegardens are prominent in the Terai region of West Bengal, while agrisilvicultural farming is not practiced in the region except for being maintained in the farms of Uttar Banga Krishi Vishwavidyalaya (UBKV), Pundibari, and thus studied with a much smaller sample size compared to forest land uses and homegardens. The age of all the agrisilvicultural systems was about 20–25 years and was intercropped with mainly paddy and winter vegetables. The biomass and carbon accumulations were comparatively much less in the agricultural systems compared to other land uses, which might be due to the smaller sampling size. Further, during the time of observation, the systems were in continuous fallow with some shrubs and herbs as weeds.
In commercial plantation crop land use systems, the order in terms of ecosystem carbon is tea plantations (141.74 Mg ha−1) > the Hevea brasiliensis plantation (87.10 Mg ha−1) > the Machilus bombycina plantation (73.66 Mg ha−1) > the Areca catechu plantation (72.19 Mg ha−1) > Cocos nucifera (71.24 Mg ha−1). Hevea brasiliensis, Cocos nucifera, and Machilus bombycina are not commercially viable plantation crops of the region and, thus, are uncommon land uses in the Terai zone of West Bengal. The sampling sizes of these plantations were also much smaller compared to other land uses. Areca nut and tea are commercial crop of the region and, thus, are a prominent land use of the Terai zone of West Bengal. Psidium guajava, Manilkara zapota, Litchi chinensis, Anacardium occidentale, Citrus lemon, and Mangifera indica are also not commercially grown in the Terai region of West Bengal and hence the sample size was small. However, in terms of ecosystem carbon accumulation, these fruit tree land uses are in the order of Mangifera indica (70.16 Mg ha−1) > Anacardium occidentale (68.18 Mg ha−1) > Manilkara zapota (66.48 Mg ha−1) > Psidium guajava (62.74 Mg ha−1) > Litchi chinensis (61.48 Mg ha−1) > Citrus lemon (60.77 Mg ha−1).
Land use management is the major option for sequestering carbon in biomass and soil viably for efficient climate change mitigation by restricting carbon emissions and capturing the atmospheric carbon as permanent storage in tree biomass and soil [100,101,102]. The best land management for longer-duration carbon storage in soil and biomass is the conversion of less or unproductive and degraded land use through rehabilitation with afforestation by restoring its SOC [103,104,105], which not only will enhance soil conditions but offset greenhouse gas emissions as well [60]. Land use conversion of inferior or degraded land through afforestation is the best climate change mitigation option because the sequestration rate through afforestation is highest (0.6 Mg C ha−1 yr−1) when compared to other mitigation options like conversion to pasture (0.5 Mg C ha−1 yr−1), organic amendments (0.5 Mg C ha−1 yr−1), residue incorporation (0.35 Mg C ha−1 yr−1), no or reduced tillage (0.3 Mg C ha−1 yr−1), and 0.2 Mg C ha−1 yr−1 for crop rotation [102].
The world’s forests were reported to be a net source of atmospheric CO2, primarily due to deforestation and degradation in the tropics [106,107]. Considering the serious issues of climate change, the remaining forests need to be conserved locally, regionally, and globally for their continuous service as the best viable climate change mitigator. However, the forests are required to be supplemented with additional carbon emission offsets through adopting the best available land management option of improving the abundant available degraded land by higher rates of carbon sequestration through afforestation. The reported available degraded land in India was 147 M ha [108]. These land uses urgently need conversion through rehabilitation by afforestation for improving the SOC and biomass carbon stock [20,21,102].
Afforestation programs for the rehabilitation of degraded lands with Tectona grandis, Shorea robusta, Michelia champaca, and Lagerstroemia parviflora is recommended as a carbon farming initiative either in the forested landscape or in the agricultural landscape as agroforestry models [20,21,109]. Sole cropping or agroforestry of Areca catechu, Cocos nucifera, Machilus bombycine, Hevea brasiliensis, and tree fruit crops can also be tried for carbon farming in the region. Moreover, short rotation tree plantations of Swietenia macrophylla, Anthocephalus cadamba, Gmelina arborea, Shorea borneensis, and Milvus migrans can be an option to sequester carbon and also to meet increasing industrial and domestic demands [87]. Tea plantations in the region can switch over to organic principles of production but needs suitable research support [47]. Agroforestry systems are ecologically sustainable as they conserves biodiversity and maintain water and soil which improves biotic interactions, buffering changes in temperature and humidity, maintenance of nutrients cycling, efficient use of light, and waste management, determining the wellbeing of people that manage them [64,110,111,112,113,114]. Several reports had indicated improvements in the productivity and creation of carbon sinks after including trees in the agricultural landscapes [115].
Homegardens are prominent landscape feature of the region but need more research and institutional support to make them more remunerative for small landowners [82,83,113,114,116]. Natural resources managed in homegardens improve the conditions of human life and sustain socio-ecological services [117,118]. Homegardens, therefore, as a system, are complementing ecological functions with a household’s needs and are now recognized as a potential model for designing socio-ecological sustainable ways of life [119]. Homegardens mimic natural forests in structure and composition [120] and the specific management practices enhance nutrient cycling and increase SOC [121]. Homegardens can enhance SOC as more than half of the carbon assimilated by woody perennials is translocated below ground via root growth and organic matter turnover processes [122]. The available status of nitrogen and organic carbon, along with the optimum soil physical characteristics estimated in the homegardens in the Terai soil of West Bengal, supported the luxurious growth and development of plants, hence carbon being sequestered by the plants and the homegarden soils. This is further supported by the fact that the homegardens with greater biodiversity also ensure the long-term stability of carbon storage in fluctuating environments, apart from augmenting biomass production potential [122]. In addition to sequestering carbon, homegardens can aid in reducing fossil fuel burning by promoting wood fuel production and conserving biodiversity [120]. They can also be instrumental in alleviating pressure from the existing natural forests [122]. The lack of stability or permanence of the carbon sequestered by a land use system is a cause of major concern in carbon sequestration projects currently. Homegardens are permanent tree-based land use systems as their biomass is never completely removed from homegardens and so are resilient [123]. The resilience and stability of the homegardens make them superior to and advantageous over the other tree-based land use systems as biomass can be completely removed from all other tree-based land use systems in the agricultural landscape.
Reports on carbon stocks across the globe indicate that significant amounts of carbon (1.1–2.2 Pg) could be sequestered over the next 30–35 years if agroforestry farming is adopted globally [124]. Agroforestry in general, and in homegardens in particular, thus gains more importance as a carbon sequestration strategy because of the carbon storage potential in its multiple plant species and soil, as well as its applicability in agricultural lands and in reforestation [64,123]. This clearly advocates agroforestry as small landholders’ land use systems in the tropics as a viable and low-cost climate change mitigation option [123]. Intensive industrialized systems have failed in sustainable issues, as their achievements were laced with high environmental costs like climate change [125]. Therefore, the remedy is searching for a new paradigm of climate-smart farming systems for sustainable food security and carbon farming. The option best suited was improving the capacities of the traditional systems like agroforestry and homegardens [126]. These traditional systems have the potential to maintain optimum productivity without losing the diversity of components and functions, while farming carbon as well [125].
The diminishing terrestrial carbon sink [18,64,127] has led to the recognition of terrestrial ecosystems in mitigating climate change globally [128,129]. The results of the present study clearly indicate that land use and land cover change (LUCC) are crucial for the distribution, magnitude, and mechanisms of terrestrial carbon sources and sinks locally and globally [128]. However, the regional patterns, magnitude, and driving mechanisms of terrestrial carbon sinks and sources are uncertain and vary across regions [128,130]. It was reported that LUCC contributes to the uncertainties in estimating the carbon fluxes in and out of the terrestrial ecosystems [131,132,133,134]. The present study also did not estimate the carbon fluxes in and out of the systems due to the absence of detailed LUCC databases of the study region [135,136,137,138]. Carbon exchange between these tree-based land use systems and the atmosphere would have generated a more accurate estimation of the carbon budgets of the Terai region of West Bengal to efficiently support policy and management decisions for climate change mitigation [139,140,141,142]. It is thus recommended, based on the results obtained from the present study, that it is necessary to include detailed dynamics of land use change while estimating the LUCC carbon at any spatial level [137]. Otherwise, it is impossible to accurately quantify the geographic distributions, magnitudes, and mechanisms of terrestrial carbon sequestration at the local to global scales. Land management through tree-based carbon farming can mitigate climate change in the true sense as it is an avoided emission [143] and transfers net carbon from the atmosphere to the land as well [103]. Tree-based land use management was a viable objective set in ambitious 4 per mille global initiative [101,102]. This is because afforestation has the potential to sequester the highest SOC as evidenced globally [94] and, thus, constitutes “true” sequestration [103].

4. Conclusions

It was evidenced that forests had the highest SOC stock with the lowest pH, higher EC and soil moisture content, and the highest availability of primary soil nutrients. Regarding ecosystem carbon accumulation, the sequence of the land uses was forests > commercial crop plantations > forest tree plantations > agroforestry > fruit orchards. Overall, the forests accumulated 3.24 times more carbon than the other tree-based land uses in agricultural landscapes. The results of the present study also indicated that land use and land cover change (LUCC) are crucial determinants for terrestrial carbon sources and sink in the region. Considering the significant differences between the SOC and the standing tree biomass among the trees-based land use systems in the Terai zone of West Bengal, it is recommended to conserve the remaining natural forests, as their conversion will cause significant emission losses of terrestrial carbon. Additionally, afforestation programs for rehabilitating degraded lands with Tectona grandis, Shorea robusta, Michelia champaca, and Lagerstroemia parviflora are recommended as carbon farming initiatives on the degraded forested landscape or the agricultural landscape. Homegardens are a prominent landscape feature of the region but need more research and institutional support to make them more remunerative for small landowners. The results obtained from the present study can be used in future research for a detailed study of ecosystem carbon dynamics along LUCC at any spatial level. The regional patterns, magnitudes, and driving mechanisms of terrestrial carbon sinks and sources are uncertain and vary across the regions. Land use and land cover change (LUCC) cause uncertainties in estimating the carbon fluxes in and out of terrestrial ecosystems. Therefore, carbon exchange between the land use systems and the atmosphere must be studied to estimate carbon budgets accurately. The detailed dynamics of land use change need to be studied while estimating the LUCC carbon to accurately quantify the geographic distributions, magnitudes, and mechanisms of terrestrial carbon sequestration at the local to global scales.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/land12061155/s1. Table S1. Effect of tree-based land-use systems on SOC (Mg ha−1) at different soil depths; Table S2. Effect of tree-based land-use systems on biomass accumulation and partitioning (Mg ha−1); Table S3. Effect of tree-based land-use systems on soil EC (dS m−1) at different depths; Table S4. Effect of tree-based land-use systems on soil pH at different depths; Table S5. Effect of tree-based land-use systems on soil moisture (%) at different depths; Table S6. Effect of tree-based land-use systems on soil available nitrogen (kg ha−1) at different depths; Table S7. Effect of tree-based land-use systems on soil available phosphorus (kg ha−1) at different depths; Table S8. Effect of tree-based land-use systems on soil available potassium (Kg ha−1) at different depths; Table S9. Effect of tree-based land-use systems on biomass carbon stock and partitioning (Mg ha−1); Table S10. Effect of tree-based land-use system on ecosystem carbon (Mg ha−1).

Author Contributions

Conceptualization, S.C.; methodology, S.C., G.S. and A.J.N.; software, resources and formal analysis, S.C., T.D. and D.S.; data curation, T.D., M.S., A.A., M.T., S.N.N. and S.C.; writing—original draft preparation, S.C., and T.D.; writing—review and editing, S.C., G.S. and A.J.N.; supervision, S.C. and G.S.; project administration, S.C.; funding acquisition, S.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data could be provided on reasonable request from the first author or corresponding author.

Acknowledgments

We would like to express our gratitude to all those who helped us during the writing of this article. The authors are thankful to the reviewers for their constructive comments to improve the quality of the paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Foley, J.A.; Defries, R.; Asner, G.P.; Barford, C.; Bonan, G.; Carpenter, S.R.; Chapin, F.S.; Coe, M.T.; Daily, G.C.; Gibbs, H.K.; et al. Global consequences of land use. Science 2005, 309, 570–574. [Google Scholar] [CrossRef]
  2. Marland, G.; Boden, T.A.; Andres, R.J. Global, regional, and national CO2 emissions. In Trends: A Compendium of Data on Global Change; Carbon Dioxide Information Analysis Centre, Oak Ridge National Laboratory, U.S. Department of Energy Oak Ridge: Oak Ridge, TN, USA, 2007. [Google Scholar]
  3. Ciais, P.; Sabine, C.; Bala, G.; Bopp, L.; Brovkin, V.; Canadell, J.; Chhabra, A.; DeFries, R.; Galloway, J.; Heimann, M.; et al. Carbon and other biogeochemical cycles. In Climate Change 2013: The Physical Science Basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change; Stocker, T.F., Qin, D., Plattner, G.-K., Tignor, M., Allen, S.K., Boschung, J., Nauels, A., Xia, Y., Bex, V., Midgley, P.M., Eds.; Cambridge University Press: Cambridge, UK; New York, NY, USA, 2013. [Google Scholar]
  4. Achard, F.; Beuchle, R.; Mayaux, P.; Stibig, H.-J.; Bodart, C.; Brink, A.; Carbonic, S.; Desclée, B.; Donnay, F.; Eva, H.D.; et al. Determination of tropical deforestation rates and related carbon losses from 1990 to 2010. Glob. Chang. Biol. 2014, 20, 2540–2554. [Google Scholar] [CrossRef]
  5. Le Quéré, C.; Moriarty, R.; Andrew, R.M.; Peters, G.P.; Ciais, P.; Friedlingstein, P.; Jones, S.D.; Sitch, S.; Tans, P.; Arneth, A.; et al. Global carbon budget. Earth Syst. Sci. Data 2015, 7, 47–85. [Google Scholar] [CrossRef]
  6. Le Quéré, C.; Peters, G.P.; Andres, R.J.; Andrew, R.M.; Boden, T.A.; Ciais, P.; Friedlingstein, P.; Houghton, R.A.; Marland, G.; Moriarty, R.; et al. Global carbon budget. Earth Syst. Sci. Data 2013, 6, 235–263. [Google Scholar] [CrossRef]
  7. Houghton, R.A. Revised estimates of the annual net flux of carbon to the atmosphere from changes in land use and land management 1850–2000. Tellus Ser. B Chem. Phys. Meteorol. 2003, 55, 378–390. [Google Scholar]
  8. Houghton, R.A.; Goodale, C.L. Effects of land-use change on the carbon balance of terrestrial ecosystems. In Ecosystems and Land Use Change; DeFries, R.S., Asner, G.P., Houghton, R.A., Eds.; American Geophysical Union: Washington, DC, USA, 2004; pp. 85–98. [Google Scholar]
  9. IPCC. Land Use, Land Use Change and Forestry: A Special Report of the Intergovernmental Panel on Climate Change (IPCC); Cambridge University Press: Cambridge, UK, 2000. [Google Scholar]
  10. Zhang, W.J.; Liu, C.H. Some thoughts on global climate change: Will it get warmer and warmer? Environ. Skept. Crit. 2012, 1, 1–7. [Google Scholar]
  11. Chakravarty, S.; Puri, A.; Vineeta; Dey, T.; Rai, P.; Pala, N.A.; Shukla, G. Climate Change Impacts vis-à-vis Biodiversity. In Forests, Climate Change and Biodiversity; Sood, K.K., Mahajan, V., Eds.; Kalyani Publishers: New Delhi, India, 2018; pp. 223–241. [Google Scholar]
  12. Heimann, M.; Reichstein, M. Terrestrial ecosystem carbon dynamics and climate feedbacks. Nature 2008, 451, 289–292. [Google Scholar] [CrossRef]
  13. McAlpine, C.A.; Ryan, J.G.; Seabrook, L.; Thomas, S.; Dargusch, P.J.; Syktus, J.I.; Pielke, R.A.; Etter, A.E.; Fearnside, P.M.; Laurance, W.F. More than CO2: A broader paradigm for managing climate change and variability to avoid ecosystem collapse. Curr. Opin. Environ. Sustain. 2010, 2, 334–346. [Google Scholar] [CrossRef]
  14. Nath, A.J.; Sileshi, G.W.; Laskar, S.Y.; Pathak, K.; Reang, D.; Nath, A.; Das, A.K. Quantifying carbon stocks and sequestration potential in agroforestry systems under divergent management scenarios relevant to India’s Nationally Determined Contribution. J. Clean. Prod. 2021, 281, 124831. [Google Scholar] [CrossRef]
  15. Reang, D.; Nath, A.J.; Sileshi, G.W.; Hazarika, A.; Das, A.K. Post-fire restoration of land under shifting cultivation: A case study of pineapple agroforestry in the Sub-Himalayan region. J. Environ. Manag. 2022, 305, 114372. [Google Scholar] [CrossRef]
  16. Lawler, J.J.; Lewis, D.; Nelson, E.; Plantinga, A.J.; Polasky, S.; Withey, C.J.; Helmers, A.P.; Martinuzzi, S.; Pennington, D.; Radeloff, V.C. Projected land-use change impacts on ecosystem services in the United States. Proc. Natl. Acad. Sci. USA 2014, 111, 7492–7497. [Google Scholar] [CrossRef]
  17. Zhang, M.; Huang, X.; Chuai, X.; Yang, H.; Lai, L.; Tan, J. Impacts of land use type conversion on carbon storage in terrestrial ecosystems of China: A spatial-temporal perspective. Sci. Rep. 2015, 5, 10233. [Google Scholar] [CrossRef] [PubMed]
  18. Lai, L.; Huang, X.; Yang, H.; Chuai, X.; Zhang, M.; Zhong, T.; Chen, Z.; Chen, Y.; Wang, X.; Thompson, J.R. Carbon emissions from land-use change and management in China between 1990-2010. Environ. Sci. 2016, 2, e1601063. [Google Scholar] [CrossRef] [PubMed]
  19. Poorter, L.; Van der Sande, M.T.; Thompson, J.; Arets, E.J.M.M.; Alarcon, A.; Alvarez- Sanchez, J.; Ascarrunz, N.; Balvanera, P.; Barajas-Guzman, G.; Boit, A.; et al. Diversity enhances carbon storage in tropical forests. Glob. Ecol. Biogeogr. 2015, 24, 1314–1328. [Google Scholar] [CrossRef]
  20. Rai, P.; Vineeta; Shukla, G.; K Manohar, A.; Bhat, J.A.; Kumar, A.; Kumar, M.; Cabral-Pinto, M.; Chakravarty, S. Carbon storage of single tree and mixed tree dominant species stands in a Reserve Forest- case study of the eastern sub-Himalayan region of India. Land 2021, 10, 435. [Google Scholar] [CrossRef]
  21. Tamang, M.; Chettri, R.; Vineeta; Shukla, G.; Bhat, J.A.; Kumar, A.; Kumar, M.; Suryawanshi, A.; Cabral-Pinto, M.; Chakravarty, S. Stand Structure, Biomass and Carbon Storage in Gmelina arborea Plantation at Agricultural Landscape in Foothills of Eastern Himalayas. Land 2021, 10, 387. [Google Scholar] [CrossRef]
  22. Kanime, N.; Kaushal, R.; Tewari, S.K.; Rivera, K.P.; Chaturvedi, S.; Chaturvedi, O.P. Biomass production and carbon sequestration in different tree-based systems of central Himalayan Terai region. For. Trees Livelihoods 2013, 22, 38–50. [Google Scholar] [CrossRef]
  23. Brahma, B.; Pathak, K.; Lal, R.; Kurmi, B.; Das, M.; Nath, A.J.; Das, A.K. (2018) Ecosystem carbon sequestration through restoration of degraded lands in Northeast India. Land Degrad. Dev. 2018, 29, 15–25. [Google Scholar] [CrossRef]
  24. Wani, A.A.; Joshi, P.K.; Singh, O.; Pandey, R. Carbon sequestration potential of Indian forestry land use systems-a review. Nat. Sci. 2012, 10, 78–85. [Google Scholar]
  25. Palm, C.; Tomich, T.; Van Noordwijk, M.; Vosti, S.; Alegre, J.; Gockowski, J.; Verchot, L. Mitigating GHG emissions in the humid tropics: Case studies from the Alternatives to Slash-and-Burn Program (ASB). Environ. Dev. Sustain. 2004, 6, 145–162. [Google Scholar]
  26. Nath, A.J.; Lal, R.; Sileshi, G.W.; Das, A.K. Managing India’s small landholder farms for food security and achieving the “4 per Thousand” target. Sci. Total Environ. 2018, 634, 1024–1033. [Google Scholar] [CrossRef]
  27. Wood, S.; Sebastian, K.; Scherr, S.J. Pilot Analysis of Global Ecosystems: Agroecosystems; International Food Policy Research Institute and World Resources Institute: Wasington, DC, USA, 2000. [Google Scholar]
  28. Chauhan, S.K.; Gupta, N.; Ritu, Y.S.; Chauhan, R. Biomass and carbon allocation in different parts of agroforestry tree species. Indian For. 2009, 135, 981–993. [Google Scholar]
  29. Keeton, W.S.; Kraft, C.E.; Warren, D.R. Mature and old- growth riparian forests: Structure, dynamics and effects on Adirondack stream habitats. Ecol. Appl. 2007, 17, 852–868. [Google Scholar] [CrossRef] [PubMed]
  30. Woodall, C.W.; Heath, L.S.; Smith, J.E. National inventories of dead and downed forest carbon stocks in the United States: Opportunities and challenges. For. Ecol. Manag. 2008, 256, 221–228. [Google Scholar] [CrossRef]
  31. Melkania, N.P. Carbon sequestration in Indian natural and planted forests. Indian For. 2009, 135, 380–387. [Google Scholar]
  32. Houghton, R.A. Aboveground Forest biomass and the global carbon balance. Glob. Chang. Biol. 2005, 11, 945–958. [Google Scholar] [CrossRef]
  33. Kurz, W.A.; Shaw, C.H.; Boisvenue, C.; Stinson, G.; Metsaranta, J.; Leckie, D.; Dyk, A.; Smyth, C.; Neilson, E.T. Carbon in Canada’s boreal forest—A synthesis. Environ. Rev. 2013, 21, 260–292. [Google Scholar] [CrossRef]
  34. Ren, H.; Chen, H.; Li, L.; Li, P.; Hou, C. Spatial and temporal patterns of carbon storage from 1992 to 2002 in forest ecosystems in Guangdong, Southern China. Plant Soil 2013, 63, 123–138. [Google Scholar] [CrossRef]
  35. Millard, P.; Sommerkorn, M.; Grelet, G. Environmental change and carbon limitation in trees: A biochemical, ecophysiological and ecosystem appraisal. New Phytol. 2007, 175, 11–28. [Google Scholar] [CrossRef] [PubMed]
  36. Kumar, P.S.; Shukla, G.; Nath, A.J.; Chakravarty, S. Soil properties, litter dynamics and biomass carbon storage in three-bamboo species of sub-Himalayan region of eastern India. Water Air Soil Pollut. 2022, 233, 12. [Google Scholar] [CrossRef]
  37. Panwar, P.; Mahalingappa, D.G.; Kaushal, R.; Bhardwaj, D.R.; Chakravarty, S.; Shukla, G.; Thakur, N.S.; Chavan, S.B.; Pal, S.; Nayak, B.G.; et al. Biomass production and carbon sequestration potential of different agroforestry systems in India: A critical review. Forests 2022, 13, 1274. [Google Scholar] [CrossRef]
  38. Pradhan, R.; Sarkar, B.C.; K Manohar, A.; Shukla, G.; Tamang, M.; Vineeta; Bhat, J.A.; Kumar, M.; Chakravarty, S. Biomass carbon and soil nutrient status in urban green sites at foothills of eastern Himalayas: Implication for carbon management. Curr. Res. Environ. Sustain. 2022, 4, 100168. [Google Scholar] [CrossRef]
  39. Pande, P.K. Litter Production and Decomposition, Mineral Release and Biochemical Diversity of Four Forest Stands at FRI Decomposition Area. Ph.D. Thesis, Garhwal University, Srinagar, India, 1986. [Google Scholar]
  40. Jackson, M.L. Soil Chemical Analysis; Prentice Hall of India Pvt. Ltd.: New Delhi, India, 1967. [Google Scholar]
  41. Piper, C. Soil and Plant Analysis: A Laboratory Manual of Methods for the Examination of Soils and the Determination of the Inorganic Constituents of Plants; Hans Publications: Bombay, India, 1966. [Google Scholar]
  42. Bray, R.M.; Kurtz, L.T. Determination of total, organic and available forms of phosphorus in soils. Soil Sci. 1945, 59, 39–45. [Google Scholar] [CrossRef]
  43. FAO. Assessing Carbon Stocks and Modelling Win-Win Scenarios of Carbon Sequestration through Land Use Changes; FAO: Rome, Italy, 2004; 156p. [Google Scholar]
  44. Kumar, B.M. Species richness and above ground carbon stocks in the homegardens of central Kerala, India. Agric. Ecosyst. Environ. 2011, 140, 430–440. [Google Scholar] [CrossRef]
  45. Brown, S. Estimating Biomass and Biomass Change of Tropical Forests: A Primer; A Forest Resources Assessment Publication, FAO Forestry; FAO: Rome, Italy, 1997; p. 134. [Google Scholar]
  46. Kalita, R.M.; Das, A.K.; Nath, A.J. Allometric equations for estimating above and below ground biomass in tea [Camellia sinensis (L.) O. Kuntze] agroforestry system of Barak Valley, Assam, Northeast India. Biomass Bioenergy 2015, 83, 42–49. [Google Scholar] [CrossRef]
  47. Kalita, R.M.; Das, A.K.; Nath, A.J. Role of smallholder tea growers in carbon sink management. Curr. Sci. 2019, 116, 1560–1566. [Google Scholar] [CrossRef]
  48. Thokchom, A.; Yadava, P.S. Biomass, carbon stock and sequestration potential of Schizostachyum pergracile bamboo forest of Manipur, north east India. Trop. Ecol. 2017, 58, 23–32. [Google Scholar]
  49. Shukla, G.; Pala, N.A.; Chakravarty, S. Carbon, litter and nutrient status in teak stands of a foothill forest in Indian eastern Himalayas. J. Tree Sci. 2014, 33, 24–32. [Google Scholar]
  50. Shukla, G.; Pala, N.A.; Chakravarty, S. Quantification of organic carbon and primary nutrients in litter and soil in a foot hill forest plantation of eastern Himalayas. J. For. Res. 2017, 28, 1195–1202. [Google Scholar] [CrossRef]
  51. Shukla, G.; Pala, N.A.; Moonis, M.; Chakravarty, S. Carbon accumulation and partitioning in sub-humid forest stands of West Bengal India. Indian For. 2018, 144, 229–233. [Google Scholar]
  52. Shukla, G.; Chakravarty, S. Biomass, primary nutrient and carbon stock in a sub-Himalayan Forest of West Bengal, India. J. For. Environ. Sci. 2018, 34, 12–23. [Google Scholar]
  53. Koul, D.N.; Panwar, P. Prioritizing land-management options for carbon sequestration potential. Curr. Sci. 2008, 95, 658–663. [Google Scholar]
  54. Koul, D.N.; Panwar, P. Opting different land use for carbon build-up in soils and their bio-economics in humid subtropics of West Bengal, India. Ann. For. Res. 2012, 55, 253–264. [Google Scholar]
  55. Koul, D.N.; Shukla, G.; Panwar, P.; Chakravarty, S. Status of soil carbon sequestration under different land use system in Terai Zone of West Bengal. Environ. We Int. J. Sci. Technol. 2011, 6, 95–100. [Google Scholar]
  56. Bhardwaj, D.R.; Sanneh, A.A.; Rajput, B.S.; Kumar, S. Status of soil organic carbon stocks under different land use systems in wet temperate north western Himalaya. J. Tree Sci. 2013, 32, 14–22. [Google Scholar]
  57. Naitham, R.; Bhattacharyya, T. Quasi-equilibrium of organic carbon in shrink–swell soils of the subhumid tropics in India under forest, horticultural, and agricultural systems. Aust. J. Soil Res. 2004, 42, 181–188. [Google Scholar] [CrossRef]
  58. Singh, G.; Rathod, T.R.; Chouhan, S. Growth, biomass production and the associated changes in soil properties in Acacia tortilis plantation in relation to plantation density in Indian arid zone. Indian For. 2004, 130, 605–614. [Google Scholar]
  59. Chhabra, A.; Dadhwal, V.K. Forest soil organic carbon pool: An estimate and review of Indian studies. Indian For. 2005, 131, 201–214. [Google Scholar]
  60. Sreenivas, K.; Dadhwal, V.K.; Kumar, S.; Harsha, G.S.; Mitran, T.; Sujatha, G.; Suresh, G.J.R.; Fyzee, M.A.; Ravisankar, T. Digital mapping of soil organic and inorganic carbon status in India. Geoderma 2016, 269, 160–173. [Google Scholar] [CrossRef]
  61. Sariyildiz, T.; Savaci, G.; Kravkaz, I.S. Effects of tree species, stand age and land-use change on soil carbon and nitrogen stock rates in north-western Turkey. iForest 2015, 9, 165–170. [Google Scholar] [CrossRef]
  62. Kimble, J.M.; Rice, C.W.; Reed, D.; Mooney, S.; Follett, R.F.; Lal, R. Soil Carbon Management: Economic, Environmental and Societal Benefits; CRC Press: Boca Raton, FL, USA, 2007. [Google Scholar]
  63. Jacobson, M.Z. Review of solutions to global warming, air pollution, and energy security. Energy Environ. Sci. 2009, 2, 148–173. [Google Scholar] [CrossRef]
  64. Hombegowda, H.C.; van Straaten, O.; Köhler, M.; Hölscher, D. On the rebound: Soil organic carbon stocks can bounce back to near forest levels when agroforests replace agriculture in southern India. Soil 2016, 2, 13–23. [Google Scholar] [CrossRef]
  65. Woomer, P.L.; Martin, A.; Albrecht, A.; Reseck, D.V.S.; Scharpenseel, H.W. The importance and management of soil organic matter in the tropics. In The Biological Management of Tropical Soil Fertility; Woomer, P.L., Swift, M.J., Eds.; Wiley Chichester: Hoboken, NJ, USA, 1994. [Google Scholar]
  66. Gairola, S.; Sharma, C.M.; Ghildiyal, S.K.; Suyal, S. Chemical properties of soils in relation to forest composition in moist temperate valley slopes of Garhwal Himalaya, India. Environmentalist 2012, 32, 512–523. [Google Scholar] [CrossRef]
  67. Paudel, S.; Sah, J.P. Physiochemical characteristic of soil in Sal (Shorea robusta) forests in eastern Nepal. Himal. J. Sci. 2003, 1, 107–110. [Google Scholar]
  68. de Hann, S. Humus, its formation, its relation with the mineral part of the soil and its significance for soil productivity. In Organic Matter Studies; International Atomic Energy Agency: Vienna, Austria, 1977; Volume 1, pp. 21–30. [Google Scholar]
  69. Weil, R.R.; Brady, N.C. The Nature and Properties of Soil, 15th ed.; Pearson Education: London, UK, 2017. [Google Scholar]
  70. Stevenson, F.J. Humus Chemistry: Genesis, Composition, Reactions, 2nd ed.; Wiley Interscience: New York, NY, USA, 1994; 512p. [Google Scholar]
  71. Sidhu, G.S.; Bhattacharyya, T.; Sarkar, D.; Ray, S.K.; Chandran, P.; Pal, D.K.; Mandal, D.K.; Prasad, J.; Nair, K.M.; Sahoo, A.K.; et al. Impact of management levels and land-use changes on soil properties in rice-wheat cropping system of the Indo-Gangetic plains. Curr. Sci. 2014, 107, 1487–1501. [Google Scholar]
  72. Singh, A.K.; Parsad, A.; Singh, B. Availability of phosphorus and potassium and its relationship with physicochemical properties of some forest soils of Pali-range (Shahodol, M.P.). Indian For. 1986, 112, 1094–1104. [Google Scholar]
  73. Raij, B. Avaliacao Da Fertilidade Do Solo; Instituto da Potassa and Fosfato: Piracicaba, Brazil, 1981; 142p. [Google Scholar]
  74. Jerabkova, L.; Prescott, C.E.; Kishchuk, B.E. Nitrogen availability in soil and forest floor of contrasting types of boreal mixed wood forests. Can. J. For. Res. 2006, 36, 112–122. [Google Scholar] [CrossRef]
  75. Shukla, G.; Chakravarty, S. Soil Carbon sequestration vis-à-vis soil management. Environ. We Int. J. Sci. Technol. 2012, 7, 107–122. [Google Scholar]
  76. Scotti, R.; Bonanomi, G.; Scelza, R.; Zoina, A.; Rao, M.A. Organic amendments as sustainable tool to recovery fertility in intensive agricultural systems. J. Soil Sci. Plant Nutr. 2015, 15, 333–352. [Google Scholar] [CrossRef]
  77. Ruess, J.O.; Innis, G.S. A grassland nitrogen flow simulation mode. Ecology 1977, 58, 348–429. [Google Scholar]
  78. Binkly, D.; Vitousek, P.M. Soil Nutrient Availability. In Plant Physiological, Field Methods and Instrumentation; Pearey, R.W., Ehleringer, J., Mooney, N.A., Rundel, P.W., Eds.; Champan and Hall: London, UK, 1989; pp. 75–96. [Google Scholar]
  79. Gupta, J.P.; Sharma, M.P.; Gupta, G.D. Characterization of Kandi belt soils of Jammu region as affected by different land use patterns. J. Indian Soc. Soil Sci. 2001, 49, 770–773. [Google Scholar]
  80. Deng, X.W.; Liu, Y.; Han, S.J. Carbon and nitrogen dynamics in early stages of forest litter decomposition as affected by nitrogen addition. J. For. Res. 2009, 20, 111–116. [Google Scholar] [CrossRef]
  81. da Gama-Rodrigues, A.C.; de Barros, N.F.; Comerford, N.B. Biomass and nutrient cycling in pure and mixed stands of native tree species in South-eastern Bahia, Brazil. Rev. Bras. De Ciência Do Solo 2007, 31, 287–298. [Google Scholar] [CrossRef]
  82. Subba, M.; Pala, N.A.; Shukla, G.; Chakravarty, S. Study of the variability of homegardens influencing carbon stock under sub-humid tropical zone of West Bengal, India. Indian For. 2018, 144, 66–72. [Google Scholar]
  83. Subba, M.; Pala, N.A.; Shukla, G.; Pradhan, K.; Chakravarty, S. Refocusing the correlates of carbon sequestration through maintaining the carbon stock in homegardens of West Bengal, India. In Natural Resources Management for Sustainable Development and Rural Livelihoods; Sati, V.P., Lalmalsawmzauva, K.C., Eds.; Today & Tomorrow’s Printers and Publishers: New Delhi, India, 2017; Volume 3, pp. 1139–1151. [Google Scholar]
  84. Behera, M.K.; Mohapatra, N.P. Biomass accumulation and carbon stocks in 13 different clones of teak (Tectona grandis Linn. F.) in Odisha, India. Curr. World Environ. 2015, 10, 1011–1016. [Google Scholar] [CrossRef]
  85. Brahma, B.; Nath, A.J.; Das, A.K. Managing rubber plantations for advancing climate change mitigation strategy. Curr. Sci. 2016, 110, 2015–2019. [Google Scholar] [CrossRef]
  86. Selvaraj, A.; Jayachandran, S.; Thirunavukkarasu, D.P.; Jayaraman, A.; Karuppan, P. Carbon sequestration potential physicochemical and microbiological properties of selected trees Mangifera indica L., Manikara zapota L., Cocus nucifera L. and Tectona grandis L. Biosci. Discov. 2016, 7, 131–139. [Google Scholar]
  87. Chauhan, S.K.; Singh, S.; Sharma, S.; Sharma, R.; Saralch, H.S. Tree biomass and carbon sequestration in four short rotation tree plantations. Range Manag. Agrofor. 2019, 40, 77–82. [Google Scholar]
  88. Gupta, D.K.; Bhatt, R.K.; Keerthika, A.; Noor Mohamed, M.B.; Shukla, A.K.; Jangid, B.L. Carbon sequestration potential of Hardwickia binata Roxb. based agroforestry in hot semi-arid environment of India: An assessment of tree density impact. Curr. Sci. 2019, 116, 112–117. [Google Scholar] [CrossRef]
  89. Ngo, K.M.; Turner, B.L.; Muller-Landau, H.C.; Davies, S.J.; Larjavaara, M.; Hassan, N.; Fbin, N.; Lum, S. Carbon stocks in primary and secondary tropical forests in Singapore. For. Ecol. Manag. 2013, 296, 81–89. [Google Scholar] [CrossRef]
  90. Slik, J.W.F.; Gary, P.; Krista, M.; Shin-Ichiro, A. Large trees drive forest aboveground biomass variation in moist lowland forests across the tropics. Glob. Ecol. Biogeogr. 2013, 22, 1261–1271. [Google Scholar] [CrossRef]
  91. Pickup, M.; Westoby, M.; Basden, A. Dry mass costs of developing leaf area in relation to leaf size. Funct. Ecol. 2005, 19, 88–97. [Google Scholar] [CrossRef]
  92. Niinemets, U.; Portsumuth, A.; Tobias, M. Leaf shape and venation pattern alter the support investments within leaf lamia in temperate species: Neglected sources of leaf physiological differentiation. Funct. Ecol. 2007, 21, 28–40. [Google Scholar] [CrossRef]
  93. Silvertown, J.W.; Doust, J.L. Introduction to Plant Population Biology; Blackwell: London, UK, 1993. [Google Scholar]
  94. Bazzaz, F.A.; Grace, J. Plant Resources Allocation; Academic Press: London, UK, 1997. [Google Scholar]
  95. Devi, L.S.; Yadava, P.S. Above ground biomass and net primary production of semi-evergreen tropical forest of Manipur, north-eastern India. J. For. Res. 2009, 20, 151–155. [Google Scholar] [CrossRef]
  96. Chhabra, A.; Dadhwal, V.K. Assessment of major pools and fluxes of carbon in Indian forests. Clim. Chang. 2004, 64, 341–360. [Google Scholar] [CrossRef]
  97. Swamy, S.L.; Puri, S.; Singh, A.K. Growth, biomass, carbon storage and nutrient distribution in Gmelina arborea Roxb, stands on red lateritic soils in central India. Bioresour. Technol. 2003, 90, 109–126. [Google Scholar] [CrossRef]
  98. Catovsky, S.; Bradford, M.A.; Hector, A. Biodiversity and ecosystem productivity: Implications for carbon storage. Oikos 2002, 97, 443–448. [Google Scholar] [CrossRef]
  99. Kirby, K.R.; Potvin, C. Variation in carbon storage among tree species implications for the management of a small-scale carbon sink project. For. Ecol. Manag. 2007, 246, 208–221. [Google Scholar] [CrossRef]
  100. Whitmore, A.P.; Kirk, G.J.D.; Rawlins, B.G. Technologies for increasing carbon storage in soil to mitigate climate change. Soil Use Manag. 2015, 31, 62–71. [Google Scholar] [CrossRef]
  101. Lal, R. Beyond COP 21: Potential and challenges of the “4 per Thousand” initiative. J. Soil Water Conserv. 2016, 71, 20A–25A. [Google Scholar] [CrossRef]
  102. Minasny, B.; Malone, B.P.; McBratney, A.B.; Angers, D.A.; Arrouays, D.; Chambers, A.; Chaplot, V.; Chen, Z.-S.; Cheng, K.; Das, B.S.; et al. Soil carbon 4 per mile. Geoderma 2017, 292, 59–86. [Google Scholar] [CrossRef]
  103. Powlson, D.S.; Whitmore, A.P.; Goulding, K.W. Soil carbon sequestration to mitigate climate change: A critical re-examination to identify the true and the false. Eur. J. Soil Sci. 2011, 62, 42–55. [Google Scholar] [CrossRef]
  104. Badgery, W.B.; Simmons, A.T.; Murphy, B.W.; Rawson, A.; Andersson, K.O.; Lonergan, V.E. The influence of land use and management on soil carbon levels for crop-pasture systems in Central New South Wales, Australia. Agric. Ecosyst. Environ. 2014, 196, 147–157. [Google Scholar] [CrossRef]
  105. Paustian, K.; Andren, O.; Janzen, H.H.; Lal, R.; Smith, P.; Tian, G.; Tiessen, H.; Van Noordwijk, M.; Woomer, P.L. Agricultural soils as a sink to mitigate CO2 emissions. Soil Use Manag. 2007, 13, 230–244. [Google Scholar] [CrossRef]
  106. Brown, S.J.; Sathaye, J.; Cannel, M.; Kauppi, P.E. Mitigation of carbon emission to the atmosphere by Forest Management. Commonw. For. Rev. 1996, 75, 80–91. [Google Scholar]
  107. Brown, S.J.; Satheya, J.; Cannel, M.; Kauppi, P. Management of forests for mitigation of greenhouse gas emissions. In Climate Change 1995: Impacts, Adaptation and Mitigation of Climate Change: Scientific-Technical Analysis; Contribution of Working Group II to the Second Assessment Report of IPCC, Chapter 24; Watson, R.T., Zinyowera, M.C., Moss, R.H., Eds.; Cambridge University Press: Cambridge, UK, 1996. [Google Scholar]
  108. Maji, A.K.; Obi Reddy, G.P.; Sarkar, D. Degraded and Wastelands of India Status and Spatial Distribution; Indian Council of Agricultural Research: New Delhi, India, 2010. [Google Scholar]
  109. Chakravarty, S.; Kumari, A.; Rai, P.; Subba, M.; Dey, T.; Lepcha, U. Forestry options as a strategy for mitigation of climate change. In Forests, Climate Change and Biodiversity; Sood, K.K., Mahajan, V., Eds.; Kalyani Publishers: New Delhi, India, 2018; pp. 197–210. [Google Scholar]
  110. Moreno-Calles, A.; Casas, A.; García-Frapolli, E. Traditional agroforestry systems of multi-crop “milpa” and “chichipera” cactus forest in the arid Tehuacán Valley, Mexico: Their management and role in people’s subsistence. Agrofor. Syst. 2012, 84, 207–226. [Google Scholar] [CrossRef]
  111. Vineeta; Sarkar, B.C.; Tamang, M.; Shukla, G.; Debnath, M.K.; Nath, A.J.; Chakravarty, S. Floristic diversity, and conservation status of large cardamom based traditional agroforestry system along an altitudinal gradient in the Darjeeling Himalaya, India. Agrofor. Syst. 2022, 96, 1199–1210. [Google Scholar] [CrossRef]
  112. Vineeta; Tamang, B.; Siril, S.; Singh, M.; Das, S.; Shukla, G.; Chakravarty, S. Ecosystem services of traditional large cardamom-based agroforestry systems of Darjeeling and Sikkim Himalayas. J. Tree Sci. 2021, 40, 78–91. [Google Scholar] [CrossRef]
  113. Roy, M.; Sarkar, B.C.; Shukla, G.; Vineeta; Debnath, M.K.; Nath, A.J.; Bhat, J.A.; Chakravarty, S. Traditional homegardens and ethnomedicinal plants: Insights from the Indian Sub-Himalayan region. Trees For. People 2022, 8, 100236. [Google Scholar] [CrossRef]
  114. Roy, M.; Sarkar, B.C.; Manohar, K.A.; Shukla, G.; Vineeta; Nath, A.J.; Bhat, J.A.; Chakravarty, S. Fuelwood species diversity and consumption pattern in the homegardens from foothills of Indian Eastern Himalayas. Agrofor. Syst. 2022, 96, 453–464. [Google Scholar] [CrossRef]
  115. Possu, W.B.; Fernando, J.; Eatrafa, N.; Jurado, H.O. An overview: The potential role of agroforestry in enhancing carbon sequestration and reducing greenhouse gas emissions on agricultural lands. Adv. Plants Agric. Res. 2018, 8, 419–430. [Google Scholar]
  116. Chakravarty, S.; Dey, T.; Pala, N.A.; Shukla, G. Mitigation, Adaptation and Coping Strategies of Forest and Farming Dependent Communities from Impacts of Global Climate Change. Indian For. 2018, 144, 1054–1062. [Google Scholar]
  117. Boege, E. El Patrimonio Biocultural de los Pueblos Indígenas de México: Hacia la Conservación in Situ de la Biodiversidad y Agrobiodiversidad de los Territorios Indígenas; Instituto Nacional de Antropología e: Historia, Mexico, 2008. [Google Scholar]
  118. Toledo, V.M.; Barrera-Bassols, N. La Memoria Biocultural: La Importancia Ecológica de las Sabidurías Tradicionales; Icaria Editorial: Barcelona, Spain, 2008. [Google Scholar]
  119. Torquebiau, E. Are tropical agroforestry homegardens sustainable? Agric. Ecosyst. Environ. 1992, 41, 189–207. [Google Scholar] [CrossRef]
  120. Kumar, B.M.; Nair, P.K.R. The enigma of tropical homegardens. Agrofor. Syst. 2004, 61, 135–152. [Google Scholar]
  121. Montagnini, F. Homegardens of Mesoamerica: Biodiversity, food security, and nutrient management. In Tropical Homegardens: A Time-Tested Example of Sustainable Agroforestry; Kumar, B.M., Nair, P.K.R., Eds.; Springer: Dordrecht, The Netherlands, 2006; pp. 61–84. [Google Scholar]
  122. Kumar, B.M. Carbon sequestration potential of tropical homegardens. In Tropical Homegardens: A Time-Tested Example of Sustainable Agroforestry; Kumar, B.M., Nair, P.K.R., Eds.; Springer Science: Dordrecht, The Netherlands, 2006; pp. 185–204. [Google Scholar]
  123. Nair, P.K.R.; Nair, V.D.; Kumar, B.M.; Showalter, J.M. Carbon sequestration in agroforestry systems. Adv. Agron. 2010, 108, 237–307. [Google Scholar]
  124. Albrecht, A.; Kandji, S.T. Carbon sequestration in tropical agroforestry systems. Agric. Ecosyst. Environ. 2003, 99, 15–27. [Google Scholar] [CrossRef]
  125. Altieri, M.A. Agroecology, small farms and food sovereignty. Mon. Rev. 2009, 61, 102–113. [Google Scholar] [CrossRef]
  126. Godfray, H.C.J.; Beddington, J.R.; Crute, I.R.; Haddad, L.; Lawrence, D.; Muir, J.F.; Pretty, J.; Robinson, S.; Thomas, S.M.; Toulmin, C. Food Security: The Challenge of Feeding 9 billion People. Science 2010, 327, 812–818. [Google Scholar] [CrossRef]
  127. Deng, L.; Zhu, G.Y.; Tang, Z.S.; Shangguan, Z.P. Global patterns of the effects of land-use changes on soil carbon stocks. Glob. Ecol. Conserv. 2016, 5, 127–138. [Google Scholar] [CrossRef]
  128. Zhao, S.Q.; Liu, S.; Sohl, T.; Young, C.; Werner, J. Land use and carbon dynamics in the southeastern United States from 1992 to 2050. Environ. Res. Lett. 2013, 8, 044022. [Google Scholar] [CrossRef]
  129. Cantarello, E.; Newton, A.C.; Hill, R.A. Potential effects of future land-use change on regional carbon stocks in the UK. Environ. Sci. Policy 2011, 14, 40–52. [Google Scholar] [CrossRef]
  130. Schlamadinger, S.; Bird, N.; Johns, T.; Brown, S.; Canadell, J.; Ciccarese, L.; Dutschke, M.; Fiedler, J.; Fiscchlin, A.; Fearnside, P.; et al. A synopsis of land use, land use change and forestry (LULUCF) under the Kyoto protocol and Marrakech Accords. Environ. Sci. Policy 2007, 10, 271–282. [Google Scholar] [CrossRef]
  131. Baccini, A.; Goetz, S.J.; Walker, W.S.; Laporte, N.T.; Sun, M.; Sulla-Menashe, D.; Hackler, J.; Beck, P.S.A.; Dubayah, R.; Friedl, M.A.; et al. Estimated carbon dioxide emissions from tropical deforestation improved by carbon-density maps. Nat. Clim. Chang. 2012, 2, 182–185. [Google Scholar] [CrossRef]
  132. Liu, S.G.; Bond-Lamberty, B.; Hicke, J.A.; Vargas, R.; Zhao, S.Q.; Chen, J.; Edburg, S.L.; Hu, Y.M.; Liu, J.X.; McGuire, A.D.; et al. Simulating the impacts of disturbances on forest carbon cycling in North America: Processes, data, models, and challenges. J. Geophys. Res. Biogeosci. 2011, 116, G00K08. [Google Scholar] [CrossRef]
  133. Liu, S.G.; Tan, Z.X.; Li, Z.P.; Zhao, S.Q.; Yuan, W.P. Are soils of Iowa USA currently a carbon sink or source? Simulated changes in SOC stock from 1972 to 2007. Agric. Ecosyst. Environ. 2011, 140, 160–162. [Google Scholar] [CrossRef]
  134. Houghton, R.A. How well do we know the flux of CO2 from land-use change? Tellus B 2010, 62, 337–351. [Google Scholar] [CrossRef]
  135. Strassmann, K.M.; Joos, F.; Fischer, G. Simulating effects of land use changes on carbon fluxes: Past contributions to atmospheric CO2 increases and future commitments due to losses of terrestrial sink capacity. Tellus Ser. B Chem. Phys. Meteorol. 2008, 60, 583–603. [Google Scholar] [CrossRef]
  136. Zhao, S.Q.; Liu, S.G.; Li, Z.P.; Sohl, T.L. Federal land management, carbon sequestration, and climate change in the southeastern US: A case study with fort Benning. Environ. Sci. Technol. 2010, 44, 992–997. [Google Scholar] [CrossRef]
  137. Zhao, S.Q.; Liu, S.; Li, Z.; Sohl, T.L. Ignoring detailed fast-changing dynamics of land use overestimates regional terrestrial carbon sequestration. Biogeosciences 2009, 6, 1647–1654. [Google Scholar] [CrossRef]
  138. Zhao, S.Q.; Liu, S.; Li, Z.; Sohl, T.L. A spatial resolution threshold of land cover in estimating terrestrial carbon sequestration in four counties in Georgia and Alabama, USA. Biogeosciences 2010, 7, 71–80. [Google Scholar] [CrossRef]
  139. Stone, B., Jr. Land use as climate change mitigation. Environ. Sci. Technol. 2009, 43, 9052–9056. [Google Scholar] [CrossRef] [PubMed]
  140. Canadell, J.G.; Kirschbaum, M.U.; Kurz, W.A.; Sanz, M.J.; Schlamadinger, B.; Yamagata, Y. Factoring out natural and indirect human effects on terrestrial carbon sources and sinks. Environ. Sci. Policy 2007, 10, 370–384. [Google Scholar] [CrossRef]
  141. Canadell, J.G.; Le Quéré, C.; Raupach, M.R.; Field, C.B.; Buitenhuis, E.T.; Ciais, P.; Conway, T.J.; Gillett, N.P.; Houghton, R.A.; Marland, G. Contributions to accelerating atmospheric CO2 growth from economic activity, carbon intensity, and efficiency of natural sinks. Proc. Natl. Acad. Sci. USA 2007, 104, 18866–18870. [Google Scholar] [CrossRef] [PubMed]
  142. Zhu, Z.L.; Bouchard, M.; Butman, D.; Hawbaker, T.; Li, Z.; Liu, J.; Liu, S.; McDonald, C.; Reker, R.; Sayler, K.; et al. Baseline and projected future carbon storage and greenhouse-gas fluxes in the Great Plains region of the United States. In US Geological Survey Professional Paper 1787; Zhu, Z.L., Ed.; USGS: Reston, VA, USA, 2011. Available online: http://pubs.usgs.gov/pp/1787/ (accessed on 1 March 2023).
  143. Sanderman, J.; Baldock, J.A. Accounting for soil carbon sequestration in national inventories: A soil scientist’s perspective. Environ. Res. Lett. 2010, 5, 034003. [Google Scholar] [CrossRef]
Figure 1. Layout map of Terai region, West Bengal.
Figure 1. Layout map of Terai region, West Bengal.
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Figure 2. Effect of land uses and soil depth on soil organic carbon.
Figure 2. Effect of land uses and soil depth on soil organic carbon.
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Figure 3. Effect of land uses and soil depth on soil electrical conductivity.
Figure 3. Effect of land uses and soil depth on soil electrical conductivity.
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Figure 4. Effect of land uses and soil depth on soil pH.
Figure 4. Effect of land uses and soil depth on soil pH.
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Figure 5. Effect of land uses and soil depth on soil moisture.
Figure 5. Effect of land uses and soil depth on soil moisture.
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Figure 6. Effect of land uses and soil depth on soil-available nitrogen.
Figure 6. Effect of land uses and soil depth on soil-available nitrogen.
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Figure 7. Effect of land uses and soil depth on soil-available phosphorus.
Figure 7. Effect of land uses and soil depth on soil-available phosphorus.
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Figure 8. Effect of land uses and soil depth on soil-available potassium.
Figure 8. Effect of land uses and soil depth on soil-available potassium.
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Figure 9. (a,b). Effect of land uses on plant biomass accumulation.
Figure 9. (a,b). Effect of land uses on plant biomass accumulation.
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Figure 10. (a,b). Effect of land uses on plant biomass carbon stock.
Figure 10. (a,b). Effect of land uses on plant biomass carbon stock.
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Figure 11. (ac). Effect of land uses on ecosystem carbon stock.
Figure 11. (ac). Effect of land uses on ecosystem carbon stock.
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Table 1. Sampling details of tree-based land uses.
Table 1. Sampling details of tree-based land uses.
Tree-Based Land Use SystemNumber of Quadrats
I. Forest landscape50
1. Lagerstroemia parviflora stand10
2. Michelia champaca stand10
3. Tectona grandis stand10
4. Shorea robusta stand10
5. Mixed-species forest10
II. Agricultural Landscape150
i. Forest Tree Plantation70
6. Swietenia macrophylla10
7. Anthocephalus cadamba10
8. Gmelina arborea10
9. Shorea borneensis10
10. Tectona grandis10
11. Lagerstroemia indica10
12. Tectona grandis + Milvus migrans5
13. Anthocephalus cadamba + Swietenia macrophylla5
ii. Agroforestry34
14. Albizia lebbeck based3
15. Swietenia macrophylla based3
16. Terminalia arjuna based3
17. Gmelina arborea based3
18. Millettia pinnata based3
19. Lagerstroemia indica based3
20. Anthocephalus cadamba based3
21. Mangifera indica based3
22. Homegardens10
iii. Commercial Crop Plantation30
23. Hevea brasiliensis3
24. Cocos nucifera3
25. Areca catechu10
26. Machilus bombycina (Som)4
27. Tea plantations10
iv. Fruit Orchard18
28. Psidium guajava3
29. Manilkara zapota3
30. Litchi chinensis3
31. Anacardium occidentale3
32. Citrus lemon3
33. Mangifera indica3
Total sample size200
Table 2. Pearson Correlation Matrix showing relationship between soil physical, chemical, and biomass in different ecosystem components.
Table 2. Pearson Correlation Matrix showing relationship between soil physical, chemical, and biomass in different ecosystem components.
ECpHMCSOCNPKPBLB
pH−0.6 **
MC0.5 **−0.4 *
SOC0.9 **−0.4 *0.5 **
N0.7 **−0.7 **0.30.9 **
P0.8 **−0.6 **0.6 **0.9 **0.7 **
K0.5 **−0.6 **0.30.8 **0.7 **0.7 **
PB0.7 **−0.5 **0.5 **0.8 **0.7 **0.7 **0.7 **
LB0.8 **−0.7 **0.4 **0.9 **0.8 **0.7 **0.7 **0.7 **
EC0.8 **−0.6 **0.5 **0.9 **0.9 **0.8 **0.8 **0.9 **0.8 **
MC—moisture content; SOC—soil organic carbon; PB—plant biomass; LB—litter biomass; BC—biomass carbon; ** Significant at the 0.01 level; * Significant at the 0.05 level.
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MDPI and ACS Style

Dey, T.; S, D.; Singh, M.; A, A.; Tamang, M.; N, S.N.; Nath, A.J.; Shukla, G.; Chakravarty, S. Prioritizing Tree-Based Systems for Optimizing Carbon Sink in the Indian Sub-Himalayan Region. Land 2023, 12, 1155. https://doi.org/10.3390/land12061155

AMA Style

Dey T, S D, Singh M, A A, Tamang M, N SN, Nath AJ, Shukla G, Chakravarty S. Prioritizing Tree-Based Systems for Optimizing Carbon Sink in the Indian Sub-Himalayan Region. Land. 2023; 12(6):1155. https://doi.org/10.3390/land12061155

Chicago/Turabian Style

Dey, Tanusri, Dinesha S, Manendra Singh, Arshad A, Mendup Tamang, Shahina N N, Arun Jyoti Nath, Gopal Shukla, and Sumit Chakravarty. 2023. "Prioritizing Tree-Based Systems for Optimizing Carbon Sink in the Indian Sub-Himalayan Region" Land 12, no. 6: 1155. https://doi.org/10.3390/land12061155

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