<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJE</journal-id><journal-title-group><journal-title>Open Journal of Ecology</journal-title></journal-title-group><issn pub-type="epub">2162-1985</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oje.2016.610057</article-id><article-id pub-id-type="publisher-id">OJE-70814</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Earth&amp;Environmental Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Aboveground Woody Biomass, Carbon Stocks Potential in Selected Tropical Forest Patches of Tripura, Northeast India
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Koushik</surname><given-names>Majumdar</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bal</surname><given-names>Krishan Choudhary</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Badal</surname><given-names>Kumar Datta</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Plant Taxonomy and Biodiversity Laboratory, Department of Botany, Tripura University, Suryamaninagar, India</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>majumdak80@gmail.com(KM)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>16</day><month>09</month><year>2016</year></pub-date><volume>06</volume><issue>10</issue><fpage>598</fpage><lpage>612</lpage><history><date date-type="received"><day>May</day>	<month>8,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>September</month>	<year>20,</year>	</date><date date-type="accepted"><day>September</day>	<month>23,</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  To estimate woody plant biomass stocks in different patches of forest ecosystems, total 20, 500 
  &#215; 
  10 m (0.5 ha) sized line transects were laid in a protected area of Tripura, Northeast India. Overall, 9160 individuals were measured at ≥10 cm diameter at breast height (dbh) in 10 ha sampled area. Estimation of biomass suggested that highest coefficient for allometric relationships between density and biomass in 10 dbh classes was observed in bamboo brakes (R<sup>2</sup> = 0.90) than lowest for semi evergreen patch (R<sup>2</sup> = 0.48). The stock of 
  carbon (C)
   was differ significantly along the forest patches (F = 7.01, df = 3.19; p &lt; 0.01). Most of biomass stock (69.38%) was accumulated in lower dbh class (&lt;30 cm) and only 23% of biomass was estimated at higher dbh classes (&gt; 70 cm). Range of biomass stock (37.85 - 85.58 Mg ha<sup>-</sup>
  <sup>1</sup>
  ) was low, compared to other tropical forest ecosystems in India, 
  which implies that the
   proper management is required to monitor regional ecosystem C pool.
 
</p></abstract><kwd-group><kwd>Woody Biomass</kwd><kwd> Potential Carbon Storage</kwd><kwd> Tropical Forest Patches</kwd><kwd> Tripura</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>World wide tropical forests are accounts about 40% of the total carbon (C) storage as terrestrial biomass [<xref ref-type="bibr" rid="scirp.70814-ref1">1</xref>] and, thus playing a fundamental role in the global C cycle [<xref ref-type="bibr" rid="scirp.70814-ref2">2</xref>] . Spatial distribution of tropical forest biomass is influenced by a range of climatic, edaphic and anthropogenic factors [<xref ref-type="bibr" rid="scirp.70814-ref2">2</xref>] . Out of total C stored in ecosystem ca.90% loses are due to loss of living biomass, an indicator of ecosystem services [<xref ref-type="bibr" rid="scirp.70814-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref3">3</xref>] . In fact, C emissions from deforestation and forest degradation are one of the most important challenges for global climate change and mitigation of greenhouse gasses [<xref ref-type="bibr" rid="scirp.70814-ref4">4</xref>] . Quantification of biomass, C and its distributions, even in local forest ecosystems comprises the significant parts of global C budget; and, thus important component of the basis for predicting future climate change [<xref ref-type="bibr" rid="scirp.70814-ref4">4</xref>] . To better understand the climate change and its impacts, information on fragmented forest patch, their biomass and C storage is still needed at regional and local scales [<xref ref-type="bibr" rid="scirp.70814-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref5">5</xref>] . Given the high rate of deforestation in tropical forest and the limited extent of old growth tropical forests [<xref ref-type="bibr" rid="scirp.70814-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref7">7</xref>] , determination of above-ground biomass (AGB) and C stocks in the remaining forest patches are the important concerns and priorities for most of the ecologist.</p><p>According to Ramachandra &amp; Shwetamala (2012) [<xref ref-type="bibr" rid="scirp.70814-ref8">8</xref>] , forest biomass contributing 74% of total C in India; and annually, 7.35% of total C emissions get stored in either forest biomass or in soil. During 1995-2005, C stocks in forest vegetation have increased from 6245 - 6662 mt, registering an annual increment of 38 mt of C or 138 mt of equivalent CO<sub>2</sub>; which recorded that forests have neutralized about 11.25% of total CO<sub>2</sub> equivalent greenhouse gas emission [<xref ref-type="bibr" rid="scirp.70814-ref9">9</xref>] . In Northeast India, numerous experiments have quantified forest biomass structure and C stock in different forest ecosystems [<xref ref-type="bibr" rid="scirp.70814-ref10">10</xref>] - [<xref ref-type="bibr" rid="scirp.70814-ref13">13</xref>] . However, it is widely recognized that Northeast India represents several virgin, natural, semi-natural and modified ecosystems due to greater variation in physiographic, climatic, edaphic and anthropogenic factors [<xref ref-type="bibr" rid="scirp.70814-ref14">14</xref>] . Tripura is the second smallest state of Northeast India, the estimation of biomass and C stock for Tripura was investigated [<xref ref-type="bibr" rid="scirp.70814-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref16">16</xref>] . In 2010, Forest survey of India (FSI) has completed estimation of forest carbon stock and change between two time period viz1994 and 2004 as part of Second National Communication [<xref ref-type="bibr" rid="scirp.70814-ref17">17</xref>] . Forest fragmentation followed by high anthropogenic pressure typically affected the forest characteristics and thereby reduced Caccumulation rate [<xref ref-type="bibr" rid="scirp.70814-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref19">19</xref>] . Since the time of earlier studies, land degradation and habitat modification have resulted serious loss of biomass stocked in this region. Tree composition and structure are the important predictive variable when estimating AGB [<xref ref-type="bibr" rid="scirp.70814-ref20">20</xref>] . Since forest structure and biomass are known to vary along different environmental gradients, including forest types and communities [<xref ref-type="bibr" rid="scirp.70814-ref20">20</xref>] ; and, even along the successional gradients [<xref ref-type="bibr" rid="scirp.70814-ref21">21</xref>] . We hypothesized that, stand density should decrease from early to late successional stages; biomass and C storage should increase from early to late stages. We also hypothesized that understanding tree age class variables are also crucial to know the differences in biomass and C stock across a successional gradient. Despite these results, C stock has yet to be studied or quantified form wide landscape levels and to be incorporated in global C estimation, especially across relatively less studied tropical moist deciduous forest ecosystem. Hence, there was a need to estimate biomass and C storage for better understanding of local forest ecosystem dynamics. Thus, overall objective of this study was set to 1) quantify first structure of woody species along different tropical moist forest patches, to 2) estimate biomass and Cstocks in different forest patches and to 3) observe how above-ground biomass and density vary from semi evergreen forest to moist deciduous vegetation patches along different age classes.</p></sec><sec id="s2"><title>2. Material and Methods</title><sec id="s2_1"><title>2.1. Study Area</title><p>We conducted our field studies in Tripura, which is the second smallest state of Northeast India with total 10,491 km<sup>2</sup> geographical area. This sanctuary covers total 194.704 km<sup>2</sup> geographical area located between 23˚05'N - 23˚25'N, and 91˚20'E - 91˚35'E (<xref ref-type="fig" rid="fig1">Figure 1</xref>), which was notified in November 1988, with total 27 revenue Mouza of Belonia, Udaipur and Sonamura Civil sub-division of South Tripura District. As per the Champion and Seth (1968) [<xref ref-type="bibr" rid="scirp.70814-ref22">22</xref>] classification system forest types of the sanctuary mainly consists of: 1) Cachar Tropical Semi Evergreen Forest 2) East Himayan lower Bhabhar</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Location of the study area and sampling points in TWS</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-1380544x2.png"/></fig><p>Moist Deciduous Sal Forest, 3) Moist Mixed Deciduous Forest, 4) Moist Bamboo Brakes and 5) Savanah Wood Land [<xref ref-type="bibr" rid="scirp.70814-ref23">23</xref>] . The elevation of the study sites ranges between 17 m to 83 m above mean sea level. The climate of this area is generally moist and humid. The minimum and maximum temperatures in summer are 21˚C and 38˚C. In winter it ranges between 4˚C and 33˚C. Humidity is generally high throughout the year. In the summer season the relative humidity differs between 50% - 74% whereas in the rainy season it is over 85%. The mean wind speed is 7.1 km/hr, with maximum of 13.1 km/h in May and minimum of 3 km/h in December. The mean annual rainfall varies between 192 - 285 cm and increased from Southwest to Northeast. The soil type of the study area is mainly red loam and sandy loam soils.</p></sec><sec id="s2_2"><title>2.2. Field Data Collection</title><p>Vegetation inventories data were collected during 2010 to 2011 by 20 line transects. Line transects were placed randomly in different forest patches in Trishna Wildlife Sanctuary. The successional gradients were identified visually following the characteristics drawn by Champion and Seth (1968) [<xref ref-type="bibr" rid="scirp.70814-ref22">22</xref>] . Out of 20 transects, 5 transects represents Moist Bamboo Brakes (MBB) dominated by Bambusa tulda, 6 transects from Moist Deciduous Sal (MDS) patch dominated by Shorea robusta, 5 transects represents Moist Mixed Deciduous (MMD) patch dominated by Schima wallichii and 4 transects from Semi Evergreen Dipterocarpus (SED) patches dominated by Dipterocarpus turbinatus. All woody individuals at ≥10 cm girth at breast height (gbh), at 1.3 m height were measured in 10 m wide and 500 m length transects. Thus, each line transect represented an area of 0.5 ha (10 &#215; 500 m) and encompassed 5 (10 &#215; 100 m) contiguous sub-plots. Specimens were identified with the help of The Flora of Tripura State [<xref ref-type="bibr" rid="scirp.70814-ref24">24</xref>] . The reference herbarium was deposited in herbarium of Botany Department; Tripura University. Information about individual species, their status including their herbarium voucher number recorded from the study site is available in a separate publication [<xref ref-type="bibr" rid="scirp.70814-ref23">23</xref>] .</p></sec><sec id="s2_3"><title>2.3. Data Analysis</title><p>Field data were quantitatively analysed on per hectare basis for density and basal area [<xref ref-type="bibr" rid="scirp.70814-ref25">25</xref>] . For estimation of woody Above Ground Biomass (AGB), regression model was used proposed by Brown et al. (1989) [<xref ref-type="bibr" rid="scirp.70814-ref26">26</xref>] due to relatively similar climatic condition of the study area (rainfall 150 - 400 cm range per year): AGB per woody species in kg (Y) = 42.69 − 12.800 (dbh) + 1.242 (dbh<sup>2</sup>) was and presented into S I unit (AGB Mg ha<sup>−1</sup>). Where, DBH ranges between 5 - 148 cm, number of sampled tree was 170 and regression coefficient (R<sup>2</sup>) = 0.84 [<xref ref-type="bibr" rid="scirp.70814-ref26">26</xref>] . Moist deciduous forest frequently dominated several bamboo species. Since, present study area was found to be dominate by Bambusa tulda; we used separate equation for biomass estimation of bamboo species [<xref ref-type="bibr" rid="scirp.70814-ref27">27</xref>] , W = a dbh<sup>b</sup>. Where, W= weight of bamboo culm in kg, dbh = diameter at breast height, allometric values for a = 0.141 and b = 2.48 with regression coefficient (R<sup>2</sup>) = 0.973 [<xref ref-type="bibr" rid="scirp.70814-ref27">27</xref>] . The estimation of Cstocks (C Mg ha<sup>−1</sup>) was calculated as 50% of the total biomass; since, C content in plant tissue is approximately half of the dry weight of aboveground live biomass [<xref ref-type="bibr" rid="scirp.70814-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref6">6</xref>] . The significance of differences in forest structural variables among the patches was statistically tested using one?way analysis of variance (ANOVA) and Tukey’s test.</p><p>To compare the size-class distributions of biomass storage in each forest patches, we plotted AGB and C Mg ha<sup>−1</sup> along ten gbh classes (&gt;10, 10.1 - 20, 20.1 - 30, 30.1 - 40, 40.1 - 50, 50.1 - 60, 60.1 - 70, 70.1 - 80, 80.1 - 90 and &gt;90 cm). The relationship between AGB Mg ha<sup>−1</sup> (y) and density ha<sup>−1</sup> (x) along teng bh classes in four different forest patches were examined and compared by linear curve fitting. The statistical analysis was performed by PAST version 1.89 [<xref ref-type="bibr" rid="scirp.70814-ref28">28</xref>] .</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><sec id="s3_1"><title>3.1. Woody Vegetation Structure</title><p>Stem density was recorded highest for MBB (1088.4 &#177; 96.15 ha<sup>−</sup><sup>1</sup>) and lowest in case of SED (701 &#177; 45.79 ha<sup>−</sup><sup>1</sup>). However, density of stems was found varied significantly (F = 4.20, df = 3.19; p = 0.02) within the forest patches. Basal area at the study sites ranged between 8.91 &#177; 1.39 m<sup>2</sup> ha<sup>−</sup><sup>1</sup> (MMD)to 33.69 &#177; 8.76 m<sup>2</sup> ha<sup>−</sup><sup>1</sup> (SED), followed by 9.17 &#177; 1.24 m<sup>2</sup> ha<sup>−</sup><sup>1</sup> in MBB and 9.05 &#177; 1.60 m<sup>2</sup> ha<sup>−</sup><sup>1</sup> in MDS. Basal area also significantly varied (F = 10.04, df = 3.19; p &lt; 0.001) among the patches. Mean stem dbh was significantly high in SED (50.56 &#177; 2.77 cm) than other patches (F = 25.88, df = 3.19; p &lt; 0.001). Even, mean canopy height (m) was also recorded high in SED (9.28 &#177; 0.97 m) and found significantly differed among the forest patches (F = 12.71, df = 3.19; p &lt; 0.001) (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>Highest stem density in MBB might be due to high abundance of Bambusa tulda (density ha<sup>−</sup><sup>1</sup>); which is locally adaptive and ecologically dominated species, facilitated</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Woody species structural variables (Mean &#177; SE) along forest patches in TWS. Variations are analyzed by ANOVA (degree of freedom 3, 19)</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Forest ecosystems</th><th align="center" valign="middle"  rowspan="2"  >Moist Bamboo Breaks (MBB)</th><th align="center" valign="middle"  rowspan="2"  >Moist Deciduous Sal (MDS)</th><th align="center" valign="middle"  rowspan="2"  >Moist Mixed Deciduous (MMD)</th><th align="center" valign="middle"  rowspan="2"  >Semi Evergreen Dipterocarpus (SED)</th><th align="center" valign="middle"  colspan="2"  >ANOVA</th></tr></thead><tr><td align="center" valign="middle" >F-value</td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Structural variables</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Density (ha<sup>−1</sup>)</td><td align="center" valign="middle" >1088.4 &#177; 96.15</td><td align="center" valign="middle" >957.60 &#177; 83.64</td><td align="center" valign="middle" >853.2 &#177; 75.93</td><td align="center" valign="middle" >701 &#177; 45.79</td><td align="center" valign="middle" >4.20</td><td align="center" valign="middle" >0.02</td></tr><tr><td align="center" valign="middle" >Basal area (m<sup>2</sup> ha<sup>−1</sup>)</td><td align="center" valign="middle" >9.17 &#177; 1.24</td><td align="center" valign="middle" >9.05 &#177; 1.60</td><td align="center" valign="middle" >8.91 &#177; 1.39</td><td align="center" valign="middle" >33.69 &#177; 8.76</td><td align="center" valign="middle" >10.04</td><td align="center" valign="middle" >0.0006</td></tr><tr><td align="center" valign="middle" >Avg. stem diameter (cm)</td><td align="center" valign="middle" >26.36 &#177; 1.09</td><td align="center" valign="middle" >29.81 &#177; 1.84</td><td align="center" valign="middle" >29.66 &#177; 2.51</td><td align="center" valign="middle" >50.56 &#177; 2.77</td><td align="center" valign="middle" >25.88</td><td align="center" valign="middle" >0.0002</td></tr><tr><td align="center" valign="middle" >Avg. canopy height (m)</td><td align="center" valign="middle" >8.91 &#177; 0.91</td><td align="center" valign="middle" >4.73 &#177; 0.25</td><td align="center" valign="middle" >5.79 &#177; 0.38</td><td align="center" valign="middle" >9.28 &#177; 0.97</td><td align="center" valign="middle" >12.72</td><td align="center" valign="middle" >0.0001</td></tr><tr><td align="center" valign="middle" >Above Ground Biomass (Mg ha<sup>−1</sup>)</td><td align="center" valign="middle" >41.84 &#177; 2.94</td><td align="center" valign="middle" >42.26 &#177; 5.91</td><td align="center" valign="middle" >37.85 &#177; 4.02</td><td align="center" valign="middle" >85.59 &#177; 17.76</td><td align="center" valign="middle" >7.01</td><td align="center" valign="middle" >0.003</td></tr><tr><td align="center" valign="middle" >Above Ground Carbon (Mg ha<sup>−1</sup>)</td><td align="center" valign="middle" >20.92 &#177; 1.47</td><td align="center" valign="middle" >20.38 &#177; 2.52</td><td align="center" valign="middle" >18.93 &#177; 2.01</td><td align="center" valign="middle" >42.80 &#177; 8.88</td><td align="center" valign="middle" >7.01</td><td align="center" valign="middle" >0.003</td></tr></tbody></table></table-wrap><p>with high regeneration abilities and greater growth rate [<xref ref-type="bibr" rid="scirp.70814-ref29">29</xref>] . Even, high growth trait of bamboo can fix atmospheric C faster than similar dbh sized of a tree. In fact, Bambusa tulda have the potentiality to shift the present forest under bamboo controlled retrogression stage. Usually, there is a high density of stems with low dbh in early and intermediate stages (e.g. MMD and MBB patches), and as dbh increases with successional trend, stem density decreases in late stage (SED patch). Negi et al. (2003) [<xref ref-type="bibr" rid="scirp.70814-ref30">30</xref>] observed that the tree types have maximum C stored in the order conifers &gt; deciduous &gt; evergreen &gt; bamboos. Instead of low stem density in SED patch (701 &#177; 45.79 ha<sup>−</sup><sup>1</sup>), basal area was significantly high (33.69 &#177; 8.76 m<sup>2</sup> ha<sup>−</sup><sup>1</sup>) due to presence of voluminous Dipterocarpus turbinatus as the representative of late successional stage. Nevertheless, forest structure changed along the successional gradient according to the general pattern of secondary succession with a gradual increase in height and basal area as described for tropical forests. In addition, Shorea robusta and Dipterocarpus turbinatus locally possess good natural regeneration trait and fast growing ability [<xref ref-type="bibr" rid="scirp.70814-ref31">31</xref>] . Therefore, these species came out as significant C sequester in this region and long term monitoring of C dynamics in those forests are possible through timescale observation on these two key dominated species. We also predicted that, significant differences in species composition and dominant trends may influence the biomass and C stock in each forest patch through control over water availability, litter and debris deposition, composition and quantity of root exudates and the distribution of C in the soil profile.</p></sec><sec id="s3_2"><title>3.2. Status of Biomass and C Stocks along the Forest Patches</title><p>The value of AGB in the whole study area, ranged between 20.86 Mg ha<sup>−</sup><sup>1</sup> (MDS) to 126.37 Mg ha<sup>−</sup><sup>1</sup> (SED). However, mean AGB was significantly greater (F = 7.01, df = 3.19; p &lt; 0.01) in SED (85.59 &#177; 17.76 Mg ha<sup>−</sup><sup>1</sup>) than recorded minimum value (37.85 &#177; 4.02 Mg ha<sup>−</sup><sup>1</sup>) in case of MMD. Highest contributor of AGC stock was SED patch (35.13 &#177; 8.88 Mg ha<sup>−</sup><sup>1</sup>) followed by MBB (22.08 &#177; 2.60 Mg ha<sup>−</sup><sup>1</sup>), MDS (19.11 &#177; 2.39 Mg ha<sup>−</sup><sup>1</sup>) and MMD (18.92 &#177; 2.01 Mg ha<sup>−</sup><sup>1</sup>), which also found significantly varied among the different patches (F = 7.01, df = 3.19; p &lt; 0.01) (<xref ref-type="table" rid="table2">Table 2</xref>). In MBB patch, Bambusa tulda contributed about 35.5% (14.46 Mg ha<sup>−</sup><sup>1</sup>) of total biomass. Other dominant tree shared less than 10% of total biomass i.e. Schima wallichii (9.21% or 3.86 Mg ha<sup>−</sup><sup>1</sup>); Terminalia bellirica (6.55% or 2.72 Mg ha<sup>−</sup><sup>1</sup>); Microcos peniculata (4% or 1.68 Mg ha<sup>−</sup><sup>1</sup>) and Lannea coromandellica (2.62% or 1.10 Mg ha<sup>−</sup><sup>1</sup>). In MDS patch, Shorea robusta was the highest contributor and shared about 56.33% (23.81 Mg ha<sup>−</sup><sup>1</sup>) of total biomass followed by Dipterocarpus turbunatus 6.09% (2.58 Mg ha<sup>−</sup><sup>1</sup>), Schima wallichii 3.33% (1.41% Mg ha<sup>−</sup><sup>1</sup>), Terminalia bellirica 3.13% (1.33 Mg ha<sup>−</sup><sup>1</sup>) and Microcos peniculata 2.14% (0.91 Mg ha<sup>−</sup><sup>1</sup>). Among the present studied forest patches, most common dominant species was Schima wallichii and it contributed about 8.1% (16.63 Mg ha<sup>−</sup><sup>1</sup>) of the total biomass of the study area. Overall, the highest contributor was Dipterocarpus turbinatus, it shared about 22.34% (46.38 Mg ha<sup>−</sup><sup>1</sup>) of total biomass (<xref ref-type="table" rid="table2">Table 2</xref>). In the present estimation of total biomass, 70% was stocked at &lt;30 cm dbh class; which indicated sufficient amount of young stems or maximum number of trees could not attained full maturity in those</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Above ground biomass and carbon contribution by top five dominant species along forest patches in TWS</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Species</th><th align="center" valign="middle"  colspan="4"  >Above Ground Biomass/Above Ground Carbon (Mg ha<sup>−1</sup>)</th></tr></thead><tr><td align="center" valign="middle" >MBB</td><td align="center" valign="middle" >MDS</td><td align="center" valign="middle" >MMD</td><td align="center" valign="middle" >SED</td></tr><tr><td align="center" valign="middle" >Aporosa octandra</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.45/0.72</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Bambusa tulda</td><td align="center" valign="middle" >14.46/7.23</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Careya arborea</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.29/0.65</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Castanopsis indica</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.06/1.03</td></tr><tr><td align="center" valign="middle" >Dipterocarpus turbinatus</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.58/1.29</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >43.80/21.90</td></tr><tr><td align="center" valign="middle" >Ficus religiosa</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.09/1.04</td></tr><tr><td align="center" valign="middle" >Holarrhena pubescens</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.10/0.55</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Lannea coromandelica</td><td align="center" valign="middle" >1.10/0.55</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Microcos paniculata</td><td align="center" valign="middle" >1.68/0.84</td><td align="center" valign="middle" >0.91/0.45</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.55/1.27</td></tr><tr><td align="center" valign="middle" >Schima wallichii</td><td align="center" valign="middle" >3.86/1.93</td><td align="center" valign="middle" >1.41/0.71</td><td align="center" valign="middle" >1.88/0.94</td><td align="center" valign="middle" >9.49/4.74</td></tr><tr><td align="center" valign="middle" >Shorea robusta</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >23.81/11.90</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Terminalia bellirica</td><td align="center" valign="middle" >2.72/1.36</td><td align="center" valign="middle" >1.33/0.66</td><td align="center" valign="middle" >2.24/1.12</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Sum of 5 most dominant</td><td align="center" valign="middle" >23.81/11.90</td><td align="center" valign="middle" >30.03/15.01</td><td align="center" valign="middle" >7.96/3.98</td><td align="center" valign="middle" >59.98/29.99</td></tr><tr><td align="center" valign="middle" >Rest other species</td><td align="center" valign="middle" >17.67/8.83</td><td align="center" valign="middle" >12.23/6.12</td><td align="center" valign="middle" >29.89/14.95</td><td align="center" valign="middle" >25.61/12.80</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >41.48/20.74</td><td align="center" valign="middle" >42.26/21.13</td><td align="center" valign="middle" >37.85/18.93</td><td align="center" valign="middle" >85.59/42.80</td></tr></tbody></table></table-wrap><p>forest patches, possibly these forest patches were recovering from significant historic disturbances. Being as early and intermediated stages MMD and MBB patches (37.85 and 41.84 Mg ha<sup>−</sup><sup>1</sup>) recover much biomass compared to MDS patch (42.26 &#177; 5.91 Mg ha<sup>−</sup><sup>1</sup>). This may due to the changes in forest composition and structure during succession, occurred at very different rates; and biomass generally recovers more rapidly than species richness [<xref ref-type="bibr" rid="scirp.70814-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref12">12</xref>] . About 40% tree species contributed &gt;70% of total biomass in dry deciduous forest [<xref ref-type="bibr" rid="scirp.70814-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref27">27</xref>] . In the present moist deciduous forest patches, five most dominant species contributed 57.41% of biomass in MBB, 70.06% in MDS, 21.02% in MMD and 70.08% in SED. Out of 5 most dominated species in all forest patches, the top dominant species contributed 34.85% biomass (Bambusa tulda) in MBB, Shorea robusta had 56.34% biomass in MDS, Terminalia bellirica had 5.92% in MMD and Dipterocarpus turbinatus contributed 51.18% biomass in SED (<xref ref-type="table" rid="table2">Table 2</xref>). Both SED and MSD forests were came out as more mature or late successional phase than other patches and might preserve much more C and also responsible for greater C management. Further, AGB recorded in the present study ranged from 20.86 Mg ha<sup>−</sup><sup>1</sup> to 126.37 Mg ha<sup>−</sup><sup>1</sup> also fall within the range of the earlier study from the area [<xref ref-type="bibr" rid="scirp.70814-ref15">15</xref>] - [<xref ref-type="bibr" rid="scirp.70814-ref17">17</xref>] , which was found less than AGB value of Central Himalaya (171.9 - 380.3 Mg ha<sup>−</sup><sup>1</sup>) [<xref ref-type="bibr" rid="scirp.70814-ref32">32</xref>] , Western Ghats (468 - 607.7 Mg ha<sup>−</sup><sup>1</sup>) [<xref ref-type="bibr" rid="scirp.70814-ref33">33</xref>] and in Eastern Ghats (15.61 - 597.13 Mg ha<sup>−</sup><sup>1</sup>) [<xref ref-type="bibr" rid="scirp.70814-ref34">34</xref>] . Present AGB value was found close to other reported value of biomass in northeast India viz. Meghalaya, Assam and Manipur [<xref ref-type="bibr" rid="scirp.70814-ref10">10</xref>] - [<xref ref-type="bibr" rid="scirp.70814-ref12">12</xref>] .</p><p>Estimation of live tree biomass is very crucial for an ecosystem, especially to understand overall ecosystem health and services including the hydrological cycle, soil erosion, nutrient cycling and dynamics of terrestrial C [<xref ref-type="bibr" rid="scirp.70814-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref6">6</xref>] . Although, our biomass and C stock means were statistically different, which suggested there was considerable variation in stand structure across the forest patches. The biomass contrast of five top most dominant trees was consistent with diversity and structural complexity. For instance, basal area, density of voluminous trees and diameter were found greater in late successional forest patch (SED) than the patches at early stages, and thereby repre- sented higher quantity of biomass and C stocks (<xref ref-type="table" rid="table1">Table 1</xref>). Results also suggest that key dominant trees make a proportionately greater contribution to total biomass as stands undergo late-successional development [<xref ref-type="bibr" rid="scirp.70814-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref21">21</xref>] . Our rationale was that local ecological factors (patch size, isolation, species composition, soils, productivity, and disturbance regimes) were accounted for variability in biomass C stock levels in those forest patches. And, succession has the potential influences to biomass development and C cycling in those forest patches.</p></sec><sec id="s3_3"><title>3.3. Distribution of Biomass and C Storage along the Age Classes</title><p>Mean maximum AGC stock was recorded from 42.80 Mg ha<sup>−</sup><sup>1</sup> (SED) to18.93 Mg ha<sup>−</sup><sup>1</sup> (MMD). The value is quite comparable with other previous estimates of biomass in different forest areas of Tripura. In India, the estimated Forest phytomass carbon density pool for the recent period are mostly in the range of 50 - 68 Mg ha<sup>−</sup><sup>1</sup>. Tripura was having phytomass C density between 0 - 25 Mg ha<sup>−</sup><sup>1</sup> in 1988 [<xref ref-type="bibr" rid="scirp.70814-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref16">16</xref>] . The cumulative net “C” flux from Indian Forests during 1888-1996, due to land use change (deforestation, afforestation and phytomass degradation) was estimated at 4.54 PgC. Using Biomass expansion factor total estimated biomass of Tripura was about 40 Mt. In Tripura average biomass density ranged from 66.7 to 83.6 Mg ha<sup>−</sup><sup>1</sup> for open forest and dense forest respectively [<xref ref-type="bibr" rid="scirp.70814-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref17">17</xref>] . While, stocks of C was substantially declined in larger dbh classes; except in case of SED patch, most stock of AGC was restricted in smaller dbh classes (&lt;30 cm) (<xref ref-type="fig" rid="fig2">Figure 2</xref>). Comparison of allometric relationships between total AGB and density distribution in different dbh classes in four tropical moist deciduous forest patches implied that there were significant differences among the AGB distribution (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Overall, 69.38% (35.73 Mg ha<sup>−</sup><sup>1</sup>) of total biomass was concentrated in &lt;30 cm dbh class and 23% at &gt;70 cm dbh class (12.08 Mg ha<sup>−</sup><sup>1</sup>). The intermediated dbh classes between &gt;30 to &lt;70 cm contributed only 7% of biomass (3.69 Mg ha<sup>−</sup><sup>1</sup>). However in MBB, 90% (37.55 Mg ha<sup>−</sup><sup>1</sup>) of biomass was represented by &lt;40 cm girth class, which indicated that the higher proportion of AGB was contributed by lower dbh classes, particularly in the form of dominated bamboo culms. Biomass distribution in 10 dbh classes was significantly varied (F = 74.13, df = 1.9; p &lt; 0.001), which showed relatively highest coefficient for allometric relationships between density and AGB in different dbh classes (equation: Y = 0.56X − 0.23, R<sup>2</sup> = 0.90; <xref ref-type="fig" rid="fig3">Figure 3</xref> MBB). In MDS patch, about 90% (36.62 Mg ha<sup>−</sup><sup>1</sup>) of AGB was concentrated in &lt;20 cm dbh class and 8% (3.35 Mg ha<sup>−</sup><sup>1</sup>) between &lt;30 to &lt;60 cm dbh class; but only 1.45% (0.59 Mg ha<sup>−</sup><sup>1</sup>) of ABG represented by higher dbh class (&gt;90 cm). Analysis showed that the allometric equation of total AGB and density distribution highly correlated (Y = 0.56X − 0.20, R<sup>2</sup> = 0.81; <xref ref-type="fig" rid="fig3">Figure 3</xref> MDS). AGB distribution was significantly higher (F = 34.59, df = 1.9; p &lt; 0.001) among the lower dbh classes which indicated that forest is either immature or recovering its maturity from historic disturbances. About 75% (28.28 Mg ha<sup>−</sup><sup>1</sup>) of AGB was contributed by &lt;20 cm dbh and about 90% of biomass (33.22 Mg ha<sup>−</sup><sup>1</sup>) by &lt;30 cm dbh class in MMD patch. In addition, analysis showed low correlation for the allometric equation (Y = 0.49X − 0.08, R<sup>2</sup> = 0.76; <xref ref-type="fig" rid="fig3">Figure 3</xref> MMD) of total AGB in MMD and AGB distribution was significantly less in the higher dbh classes (F = 25.25, df = 1.9; p &lt; 0.001). Whether in case of SED patch, only 51% (44.33 Mg ha<sup>−</sup><sup>1</sup>) of AGB was shared by &lt;60 cm dbh class and 39% (33.55 Mg ha<sup>−</sup><sup>1</sup>) contributed by due to &gt;90 cm dbh; whereas total AGB as a function of density distribution in dbh classes showed low correlation (Y = 0.35X − 0.31, R<sup>2</sup> = 0.48; <xref ref-type="fig" rid="fig3">Figure 3</xref> SED), significantly high biomass storage among the larger dbh classes (F = 7.41, df = 1.9; p &lt; 0.05). Among the tree species, Dipterocarpus turbinatus (43.80 Mg ha<sup>−</sup><sup>1</sup>) accounted highest AGB in SED patch followed by Shorea robusta (23.81 Mg ha<sup>−</sup><sup>1</sup>) for MDS patch, Bambusa tulda (14.46 Mg ha<sup>−</sup><sup>1</sup>) for MBB patch and Terminalia bellirica (2.24 Mg ha<sup>−</sup><sup>1</sup>) for MMD patch (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>Likewise, Day et al. (2014) also reported high variability in biomass distribution, but in general more diverse forest tends to be accumulating more biomass [<xref ref-type="bibr" rid="scirp.70814-ref35">35</xref>] . In spite of having highest species richness, MMD had lowest value of biomass (37.85 &#177; 4.02); even, there was also relatively low coefficient (R<sup>2</sup> = 0.76; p &lt; 0.01) for allometric relationships between density distribution and AGB (<xref ref-type="fig" rid="fig3">Figure 3</xref> MMD). Similarly tree density was</p><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Distribution of Above Ground Carbon Mg ha<sup>−1</sup> along different diameter classes in four major forest types in TWS</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-1380544x3.png"/></fig><p>highest for MBB (1088.4 &#177; 96.15), but it had lower value of biomass (41.84 &#177; 2.94) showed relatively highest coefficient value (R<sup>2</sup> = 0.90; p &lt; 0.001) for allometric relationships between density distribution and AGB (<xref ref-type="fig" rid="fig3">Figure 3</xref> MBB). Inverse to that, SED</p><fig-group id="fig3"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Relationship between log transformed AGB and density ha<sup>−</sup><sup>1</sup> in different dbh classes along major forest patches (MBB, MDS, MMD and SED) in Trishna Wildlife Sanctuary of Tripura, Northeast India.</title></caption><fig id ="fig3_1"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-1380544x4.png"/></fig><fig id ="fig3_2"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-1380544x5.png"/></fig><fig id ="fig3_3"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-1380544x6.png"/></fig><fig id ="fig3_4"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-1380544x7.png"/></fig></fig-group><p>had highest amount of biomass stock (85.59 &#177; 17.76) but was relatively lowest correlation coefficient (R<sup>2</sup> = 0.48; p &lt; 0.05) for equation relationships (<xref ref-type="fig" rid="fig3">Figure 3</xref> SED); which may due to low density and irregular distribution of trees along the dbh classes. This may further be able to explain by the fact that differences in tree composition and dominance of the species along the patches, and more importantly this may related to the forest successional age [<xref ref-type="bibr" rid="scirp.70814-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.70814-ref21">21</xref>] . On the basis of biomass stocked in all dbh classes, SED patch found different from rest other three types; where trees in higher dbh class &gt;90 cm stocked maximum biomass (40%) and might represented that this forest community has comparatively reached to its maximum potential in terms of sequestration of CO<sub>2</sub>. Surprisingly, Bambusa tulda in MBB patch contributed about 35% of biomass, this shows that bamboo patch could capture considerable amount of CO<sub>2</sub> within very early stage. C pool in the above ground biomass of village bamboo in Assam increased from 21.69 Mg ha<sup>−</sup><sup>1</sup> to 76.55 Mg ha<sup>−</sup><sup>1</sup> within three years [<xref ref-type="bibr" rid="scirp.70814-ref14">14</xref>] . The recovery of biodiversity and biomass in tropical moist deciduous forest patches provides hope that they are helping to sequester considerable amount of atmospheric C. It is predicted that present trends will change over time when the early stages will grow into more mature layers and subsequently increase total biomass and C stock in those patches in course of secondary succession. In addition, sapling or regenerating woody stems density was high in MMD and MBB patches; which suggested that these forest patches can provide important ecosystem services as C sequestration. Since the regenerating stage of most woody species can sequester considerable amount of CO<sub>2</sub> by reducing it into biomass [<xref ref-type="bibr" rid="scirp.70814-ref18">18</xref>] . Our result also supporting the potentiality of fragmented village bamboo patches for quick C sequestration; and, this is due to bamboo rapid growth rate, easy multiplication ability and high biomass production. In fact, C assimilation in bamboo plantation is 16% - 20% more compared to other planted tree species i.e. Dalbergia sissoo (11.11%), Terminalia arjuna (12.07%) and natural forest of Shorea robusta (3.34%) [<xref ref-type="bibr" rid="scirp.70814-ref14">14</xref>] .</p></sec></sec><sec id="s4"><title>4. Conclusion</title><p>In this present study, depending on heterogeneity in forest patches the amount of biomass and C stock determined and found differed significantly. Species specific biomass structure and its distribution along different dbh classes are very important to know C dynamics and its sequestration processes. Besides AGB, it would be more crucial if C accumulation rates in below ground biomass, dead material, and soil along the landscapes specifically could be estimated. Even, studies also required to understand the key processes of biomass and C accumulation through time scale investigation in those forest patches. There are wide variations in terms of biomass distribution and C storage in the patch area, which suggested that present forest patches have huge potentiality as C sequestration and stocked it in the form of biomass. Climate change mitigations by restoring CO<sub>2</sub> through different local forest patches have great advantages like conservation of other species and other ecological services. Hence, it is possible that small forest patches or fragmented forest landscapes may claim enough incentive by demanding fund against management of local landscapes for restoration of CO<sub>2</sub> and conservation of biodiversity. Present quantitative structural attributes of small forest patches will be vital in future to understand C dynamics in small forest patches including the role of dominant community, niche attributes, successional trend, effects of edge and on-going disturbances on the distribution and population of threatened species.</p></sec><sec id="s5"><title>Cite this paper</title><p>Majumdar, K., Choudhary, B.K. and Datta, B.K. (2016) Aboveground Woody Biomass, Carbon Stocks Potential in Selected Tropical Forest Patches of Tripura, Northeast India. Open Journal of Ecology, 6, 598-612. http://dx.doi.org/10.4236/oje.2016.610057</p></sec></body><back><ref-list><title>References</title><ref id="scirp.70814-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Day, M., Cristina, B., Sunderland, E.R. and Terry, C.H. (2014) Environmental Conservation: Relationships between Tree Species Diversity and Above-Ground Biomass in Central African Rainforests: Implications for REDD. Environmental Conservation, 41, 64-72.http://dx.doi.org/10.1017/S0376892913000295</mixed-citation></ref><ref id="scirp.70814-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Mohanraj, R., Saravan, J. and Dhanakumar, S. (2011) Carbon Stock in Kolli Forests, Eastern Ghats (India) with Emphasis on Aboveground Biomass, Litters, Woody Debris and Soil. iForest, 4, 61-65. http://dx.doi.org/10.3832/ifor0568-004</mixed-citation></ref><ref id="scirp.70814-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Swamy, H.R. (1989) Study of Organic Productivity, Nutrient Cycling and Small Watershed Hydrology in Natural Forests and in Monoculture Plantations in Chikamagalur District, Karnataka, Final Report, Sri Jagadguru Chandrashekara Bharti Memorial College, Sringeri.</mixed-citation></ref><ref id="scirp.70814-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Gairola, S., Sharma, C.M., Ghildiyal, S.K. and Suyal, S. (2011) Live Tree Biomass and Carbon Variation along an Altitudinal Gradient in Moist Temperate Valley Slopes of the Garhwal Himalaya (India). Current Science, 100, 1862-1870.</mixed-citation></ref><ref id="scirp.70814-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Majumdar, K., Shankar, U. and Datta, B.K. (2012) Tree Species Diversity and Stand Structure along Major Community Types in Lowland Primary and Secondary Moist Deciduous Forests in Tripura, Northeast India. Journal of Forestry Research, 23, 553-568. http://dx.doi.org/10.1007/s11676-012-0295-8</mixed-citation></ref><ref id="scirp.70814-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Negi, J.D.S., Manhas, R.K. and Chauhan, P.S. (2003) Carbon Stocks in Different Components of Some Tree Species of India: A New Approach for Carbon Estimation. Current Science, 85, 1528-1531.</mixed-citation></ref><ref id="scirp.70814-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Majumdar, K., Das, P. and Datta, B.K. (2012) Seed Germination and Growth of Bambusa tulda Roxb. in Tree Cavity : An Accidental Phenomenon. Nebio, 3, 128-130.</mixed-citation></ref><ref id="scirp.70814-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Hammer, O., Harper, D.A.T. and Ryan, P.D. (2009) PAST-Palaeontological Statistics, ver. 1.89. University of Oslo, Oslo.</mixed-citation></ref><ref id="scirp.70814-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Maki, F., Mamoru, K., Maung, T.H. and Yazar, M. (2007) Recovery Process of Fallow Vegetation in the Traditional Karen Swidden Cultivation System in the Bago Mountain Range, Myanmar. Southeast Asian Studies, 45, 317-333.</mixed-citation></ref><ref id="scirp.70814-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Brown, S., Gillespie, A. and Lugo, A.E. (1989) Biomass Estimation Methods for Tropical Forests with Applications to Forest Inventory Data. Forest Science, 35, 881-902.</mixed-citation></ref><ref id="scirp.70814-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Muller, D.D. and Ellenberg, H. (1974) Aims and Methods of Vegetation Ecology. John Wiley and Sons Inc, Hoboken.</mixed-citation></ref><ref id="scirp.70814-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Deb, D.B. (1981-1983) The Flora of Tripura State. Vols. 1-2, Today and Tomorrow’s Printers and Publishers, New Delhi.</mixed-citation></ref><ref id="scirp.70814-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Majumdar, K. and Datta, B.K. (2014) A Quantitative Checklist of Woody Angiosperm Diversity, Population Structure and Habitat Grouping in Trishna Wildlife Sanctuary of Tripura, Northeast India. Check List, 10, 976-996. http://dx.doi.org/10.15560/10.5.976</mixed-citation></ref><ref id="scirp.70814-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Champion, H.G. and Seth, S.K. (1968) A Revised Forest Types of India. Manager of Publications, Government of India, Delhi.</mixed-citation></ref><ref id="scirp.70814-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Lasky, J.R., Uriarte, M., Boukili, V.K., Erickson, D.L., John Kress, W. and Chazdon, R.L. (2014) The Relationship between Tree Biodiversity and Biomass Dynamics Changes with Tropical Forest Succession. Ecology Letters, 17, 1158-1167. http://dx.doi.org/10.1111/ele.12322</mixed-citation></ref><ref id="scirp.70814-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Houghton, R.A. (2005) Aboveground Forest Biomass and the Global Carbon Balance. Global Change Biology, 11, 945-958. http://dx.doi.org/10.1111/j.1365-2486.2005.00955.x</mixed-citation></ref><ref id="scirp.70814-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Pan, Y., Birdsey, R.A., Fang, J., Houghton, R., Kauppi, P.E., Kurz, W.A. and Philips, O.L (2011) A Large and Persistent Carbon Sink in the World’s Forests. Science, 333, 988-993. http://dx.doi.org/10.1126/science.1201609</mixed-citation></ref><ref id="scirp.70814-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Phillips, O.L., Malhi, Y., Higuchi, N., Laurance, W.F., Nunez, P.V., Vasquez, R.M., Laurance, S.G., Ferreira, L.V., Stern, M., Brown, S. and Grace, J. (1998) Changes in the Carbon Balance of Tropical Forest: Evidence from Long-Term Plots. Science, 282, 439-442. http://dx.doi.org/10.1126/science.282.5388.439</mixed-citation></ref><ref id="scirp.70814-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Sharma, C.M., Baduni, N.P., Gairola, S., Ghildiyal, S.K. and Suyal, S. (2010) Tree Diversity and Carbon Stocks of Some Major Forest Types of Garhwal Himalaya, India. Forest Ecology and Management, 260, 2170-2179. http://dx.doi.org/10.1016/j.foreco.2010.09.014</mixed-citation></ref><ref id="scirp.70814-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Ramachandran, A., Jayakumar, S., Haroon, R.M., Bhaskaran, A. and Arockiasamy, D.I. (2007) Carbon Sequestration: Estimation of Carbon Stock in Natural Forests Using Geospatial Technology in the Eastern Ghats of Tamil Nadu, India. Current Science, 92, 323-331.</mixed-citation></ref><ref id="scirp.70814-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">IPCC (1996) Climate Change Impacts, Adaptations and Mitigation of Climate: Scientifc Technical Analyses. In: Contribution of II to the Second Assessment Report of the Intergovernmental Panel on Climate Change, Cambridge University Press, Cambridge.</mixed-citation></ref><ref id="scirp.70814-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">FSI (2010) State of the Forest Report 2010. Forest Survey of India, Ministry of Environment and Forest, Goverment of India, Dehradun.</mixed-citation></ref><ref id="scirp.70814-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Chhabra, A. and Dadhwal, V.K. (2004) Assessment of Major Pools and Fluxes of Carbon in Indian Forests. Climatic Change, 64, 341-360. http://dx.doi.org/10.1023/B:CLIM.0000025740.50082.e7</mixed-citation></ref><ref id="scirp.70814-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Chhabra, A., Palria, S. and Dadhwal, V.K. (2002) Growing Stock-Based Forest Biomass Estimate for India. Biomass and Bioenergy, 22, 187-194. http://dx.doi.org/10.1016/S0961-9534(01)00068-X</mixed-citation></ref><ref id="scirp.70814-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Rao, R.R. (1994) Biodiversity in India: Floristic Aspects. Bishen Singh Mahendra Pal Singh, Dehra Dun.</mixed-citation></ref><ref id="scirp.70814-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Nath, A.J. and Das, A.K. (2011) Carbon Storage and Sequestration in Bamboo-Based Smallholder Homegardens of Barak Valley, Assam. Current Science, 100, 229-233.</mixed-citation></ref><ref id="scirp.70814-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Thokchom, A. and Yadava, P.S. (2013) Biomass and Carbon Stock Assessment in the Sub-Tropical Forests of Manipur, North-East India. International Journal of Ecology Environmental Science, 39, 107-113.</mixed-citation></ref><ref id="scirp.70814-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Borah, N., Nath, A.J. and Das, A.K. (2013) Aboveground Biomass and Carbon Stocks of Tree Species in Tropical Forests of Cachar District, Assam, Northeast India. International Journal of Ecology Environmental Science, 39, 97-106.</mixed-citation></ref><ref id="scirp.70814-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Baishya, R., Barik, S.K. and Upadhaya, K. (2009) Distribution Pattern of Aboveground Biomass in Natural and Plantation Forests of Humid Tropics in Northeast India. Tropical Ecology, 50, 295-304.</mixed-citation></ref><ref id="scirp.70814-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">MoEF (2009) India’s Fourth National Report to the Convention on Biological Diversity. New Delhi: Ministry of Environment and Forests, Government of India.</mixed-citation></ref><ref id="scirp.70814-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Ramachandra, T.V. and Shwetmala (2012) Decentralised Carbon Footprint Analysis for Opting Climate Change Mitigation Strategies in India. Renewable and Sustainable Energy Reviews, 16, 5820-5833. http://dx.doi.org/10.1016/j.rser.2012.05.035</mixed-citation></ref><ref id="scirp.70814-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Sodhi, N.S., Koh, L.P., Brook, B.W. and Ng, P.K.L. (2004) Southeast Asian Biodiversity: An Impending Disaster. Trends in Ecology and Evaluation, 19, 654-660. http://dx.doi.org/10.1016/j.tree.2004.09.006</mixed-citation></ref><ref id="scirp.70814-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Malhi, Y. and Grace, J. (2000) Tropical Forests and Atmospheric Carbon Dioxide. Trends in Ecology and Evaluation, 15, 332-337. http://dx.doi.org/10.1016/S0169-5347(00)01906-6</mixed-citation></ref><ref id="scirp.70814-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Dixon, R.K., Brown, S.A., Houghton, R.A., Solomon, A.M., Trexler, M.C. and Wisniewski, J. (1994) Carbon Pools and Flux of Global Forest Ecosystems. Science, 263, 185-190. http://dx.doi.org/10.1126/science.263.5144.185</mixed-citation></ref><ref id="scirp.70814-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Brown, S., Hall, C.A.S., Knabe, W., Raich, J., Trexler, M.C. and Woomer, P. (1993) Tropical Forests: Their Past, Present and Potential Future Roles in the World’s Carbon Budget. Water Air Soil Pollution, 70, 71-94. http://dx.doi.org/10.1007/BF01104989</mixed-citation></ref></ref-list></back></article>