• google scholor
  • Views: 3687

  • PDF Downloads: 316

Biomass Allocation and Carbon Stock in Elm (Ulmus Wallichiana Planch) Plantation

Shabir Ahmad Rather1 , K.N. Qaisar1 , Sabeena Nabi1 , R. Banyal2 , P.A. Khan1 and M.A. Islam1

1 Faculty of Forestry, SKUAST-K, Ganderbal-191201 (J&K), India

2 Central Soil Salinity Research Institute, Karnal, Haryana, India

DOI: http://dx.doi.org/10.12944/CWE.12.2.17

The present investigation was conducted on a 22- year old Elm plantation established at Wadura campus of SKUAST-Kashmir. Four diameter classes viz., D1 (5-10cm), D2 (10-15cm), D3 (15-20cm) and D4 (>20cm) were stratified from the plantation and 24 trees (6 from each diameter class) were randomly selected and felled in the year 2015. The growth parameters of the trees increased with increase in the diameter class. The maximum height, dbh, basal area and stem volume were 14.98m, 23.77cm, 0.044m2 and 0.400m3, respectively. Biomass per tree of all tree components viz., stem, branches, foliage and roots showed significant increase with increase in the diameter of the trees. The total biomass, carbon stock and carbon dioxide equivalent increased from lower to higher diameter classes. The highest values observed for these parameters were 475.54 kg/tree (fresh), 148.59 kg/tree and 543.82 kg/tree, respectively under D4 diameter class. The biomass allocation coefficient of branch and root (BACb and BACr) attained higher values in lower diameter classes. The maximum and minimum values of these coefficients were 0.158 and 0.085; 0.298 and 0.278, respectively under D1 and D4 diameter classes. The size of trees did not produce significant effect on the biomass allocation coefficient of foliage (BACf). The diameter of the trees produced non-significant difference in the growth efficiency (GE) of different tree components.


Elm; Growth parameters; Carbon stock; Biomass allocation; Tree components

Copy the following to cite this article:

Rather S. A, Qaisar K. N, Nabi S, Banyal R, Khan P. A, Islam M. A. Biomass Allocation and Carbon Stock in Elm (Ulmus Wallichiana Planch) Plantation. Curr World Environ 2017;12(2). DOI:http://dx.doi.org/10.12944/CWE.12.2.17

Copy the following to cite this URL:

Rather S. A, Qaisar K. N, Nabi S, Banyal R, Khan P. A, Islam M. A. Biomass Allocation and Carbon Stock in Elm (Ulmus Wallichiana Planch) Plantation. Curr World Environ 2017;12(2). Available from: http://www.cwejournal.org/?p=17240


Download article (pdf)
Citation Manager
Publish History


Article Publishing History

Received: 2017-03-18
Accepted: 2017-06-01

Introduction

Ulmus wallichiana, the Himalayan Elm, is a fast growing tree species which grows in Himalayas from Kashmir to Uttarakhand between the elevations of 900 to 3000m amsl. The Himalayan Elm grows to a height of about 30m, with a broad crown having several ascending branches. The bark of the trunk is vertically furrowed and grayish brown in colour. Before the introduction of populous deltoides, it was the most cultivated tree species of the Kashmir valley having multifarious uses viz., light construction, fuelwood, packing cases, furniture and fodder for cattle.1  

Ever increasing atmospheric CO2 concentration and its management is a serious concern confronting the world today. The concentration of CO2 in the atmosphere can be reduced either by limiting emissions or by taking CO2 out from the atmosphere and stored in the terrestrial, oceanic or aquatic ecosystems. Forestry practices have the significant potential to considerably reduce the global flux CO2 into the atmosphere. In the past forestry plantations only had a small contribution to the total balance of terrestrial carbon but they have been recognized to play a more significant role in the future mitigation of climate change on account of their potential to absorb and store carbon.2 According to FAO, the world’s forest plantation accounted for less than 7% or 264 million ha of total forest area, in which 78% are productive and 22% are protective. The world’s forests are estimated to store 289 gigatonnes (Gt) of carbon (C) in their biomass alone and on account of deforestation the annual decrease in the carbon storage was about 0.5 Gt during the period 2005-2010.3 The total carbon storage in forest plantations now-a-days is about 11.8 Gt with an increase of 0.178 Gt per year. Furthermore, the United Nations Framework Convention on Climate Change has recognized the significance of plantation forestry as a greenhouse gas mitigation option, as well as the need to monitor, preserve, and enhance terrestrial carbon stocks.4 Due to fast growth and better silvicultural practices and management, plantation forestry has an edge over natural forests. Projections of the International Centre for Research in Agroforestry suggest that significant funds could potentially be available to finance sustainable rural development and adaptation to climate change, as the carbon market may exceed US $1 trillion by 2025.5 In view of the crucial role played by the plantations in carbon mitigation, the present study was undertaken with the objective to determine the biomass and carbon in the Elm plantation under temperate conditions.

Material and Methods

The study was carried out on a 22- year old plantation of Elm located at an altitude of 1510m amsl in the Faculty of Agriculture, SKUAST-K, Wadura, Sopore (J&K). The plantation falls in the temperate zone and lies at 34o3¢N latitude and 74o5¢E longitude. The trees in the plantation were stratified into four diameter classes i.e., D1: 5-10cm, D2: 10-15cm, D3: 15-20cm and D4: >20cm. Twenty four trees were randomly selected from the plantation (six from each diameter class) and harvested during the year 2015 for biomass and carbon estimation. These trees were measured for their growth parameters using standard biometric methods. The allocation of biomass to different tree components, growth efficiency, carbon stock and carbon dioxide equivalent were estimated as follows:

Stem biomass (Bs) (kg)

The main stem of each tree was cut into logs of different lengths. Fresh weight of these logs was recorded with the help of mechanical weighing balance and summed up to give stem biomass. Sample discs from each log were taken for dry weight determination.

Branch biomass (Bb) (kg)

Branches from each tree were cut and weighed in the field for estimation of branch biomass. The branch samples were collected from the trees for dry weight   determination.

Foliage biomass (Bf) (kg)

The foliage biomass was estimated by collecting the foliage from each felled tree and weighing in the field. The samples of foliage from the trees were taken for estimation of dry matter.

Root biomass (Br) (kg)

The root biomass was calculated by using simple default value of 25% (for hardwood species) of the above ground biomass as recommended by IPCC.6

Total tree biomass (Bt) (kg)

The total tree biomass was calculated as the sum of stem, branch, foliage and root biomass.

Biomass allocation coefficients (BACs)

Biomass allocation coefficients were calculated as the ratio between a particular biomass component increment and stem biomass increment.

Growth efficiency (GE)

Growth efficiency was estimated as the ratio of relevant biomass component increment to standing foliage biomass.

Carbon stock (kg)

The biomass value was converted to carbon stock using 0.5 default value.6

Carbon dioxide equivalent (CO2e) (kg)

It was calculated by multiplying carbon stock with 3.66.

The data generated was analyzed statistically using general linear model procedure of SPSS Statistic version (17.0).

Statistical Analysis

The data collected was subjected to statistical analysis using general linear model procedure of SPSS Statistic version (17.0).

Results and Discussion

The growth parameters of the trees increased with increase in the diameter class (Table-1). The maximum values recorded for height, dbh, basal area and stem volume were 14.98m, 23.77cm, 0.005m2 and 0.400m3 under diameter class D4 and minimum 07.67m, 08.08cm, 0.044m2 and 0.027m3 under D1 class, respectively. These observations are in line with the results of Bohre et al7 & Arifin et al8. This can be attributed to

Table 1: Growth parameters of 22- year old Ulmus wallichiana trees

Diameter class (cm)

Height (m)

dbh (cm)

Basal area (m2)

Stem volume (m3)

D1 (5-10)

07.67

08.08

0.005

0.027

D2 (10-15)

11.25

13.06

0.013

0.093

D3 (15-20)

13.57

16.95

0.023

0.187

D4 (>20)

14.98

23.77

0.044

0.400

CD (0.05)

1.52

1.78

0.004

0.064


more absorption of nutrients and light by the dominant trees present in the plantation. Yeboah et al9 found strong correlation between dbh and total main stem volume of the trees. Also, Islam and Masoodi10 reported strong positive correlation between dbh, height and stem volume in Elm. The pattern of biomass allocation in different tree components, carbon stock and carbon dioxide equivalent are depicted in the Table-2 and 3. The critical appraisal of the data revealed that stem biomass gradually increased with increase in the size of trees attaining highest values of 368.28 kg/tree (fresh) and 212.22 kg/tree (dry) in D4 diameter class. The lowest values of 23.50 kg/tree (fresh) and 12.37 kg/tree (dry) were recorded under diameter class D1. The results corroborate the observations of Wagay11 and Mitra et al12. The allocation of biomass to branches observed perpetual increment with the rise in diameter of trees. The maximum branch biomass of 34.95 kg/tree (fresh) and 18.98 kg/tree (dry) was produced by diameter class D4 whereas, the minimum of 03.34 kg/tree (fresh) and 01.98 kg/tree (dry) was observed under D1 diameter class. The branch biomass depends on the average number of branches on the trees. The results of Pande et al13 & Singh et al14 fully support the current observations. There was an increase in foliage biomass from lower to higher diameter classes recording highest values of 16.20 kg/tree (fresh) and 6.54 kg/tree (dry) for diameter class D4. The reason for such a pattern is the occurrence of more number of branches in the large sized trees than the smaller ones. Similar results have been obtained by Wagay11 in Populus deltoides. The root biomass was found to increase with increase in the diameter of the trees. The maximum and minimum root biomass of 105.11 kg/tree (fresh) and 07.07 kg/tree (fresh) were observed under diameter classes D4 and D1, respectively.  This is in conformity with the results of Saralach15 in Eucalyptus. These results of biomass are also well supported by Morhart et al16 who reported strong correlation between dry weight of different tree components and dbh in a poplar clone.

Table 2: Pattern of biomass (fresh) allocation to different tree components of 22- year old Ulmus wallichiana in different diameter classes

Diameter class (cm)

Stem biomass (fresh) (kg/tree)

Branch biomass (fresh) (kg/tree)

Foliage biomass (fresh) (kg/tree)

Root biomass (fresh) (kg/tree)

Total tree biomass (fresh) (kg/tree)

D1 (5-10)

23.50

03.34

01.45

07.07

35.36

D2 (10-15)

79.48

09.27

04.07

23.20

116.02

D3 (15-20)

137.33

19.68

08.75

41.44

207.20

D4 (>20)

369.28

34.95

16.20

105.11

475.54

CD (0.05)

56.44

08.40

03.70

16.44

89.08


Table 3: Pattern of biomass (dry) allocation to different tree components of 22- year old Ulmus wallichiana in different diameter classes

Diameter class (cm)

Stem biomass (dry) (kg/tree)

Branch biomass (dry) (kg/tree)

Foliage biomass (dry) (kg/tree)

Root biomass (dry) (kg/tree)

Total tree biomass (dry) (kg/tree)

Carbon stock (kg/tree)

CO2e (kg/tree)

D1 (5-10)

12.37

01.98

0.51

03.71

18.57

09.29

33.99

D2(10-15)

42.47

05.29

1.51

12.25

61.52

30.78

112.66

D3 (15-20)

75.65

10.83

3.35

22.46

112.29

56.14

205.46

D4 (>20)

212.22

18.98

6.54

59.43

297.17

148.59

543.82

CD(0.05)

31.54

04.66

01.52

09.08

46.04

23.02

84.26


CO2 e = Carbon dioxide equivalent

The total dry biomass, carbon stock and carbon dioxide equivalent increased from lower to higher diameter classes. The highest values for these parameters were 297.17 kg/tree, 148.59 kg/tree and 543.82 kg/tree, respectively under D4 diameter class and the lowest values of 18.57 kg/tree, 09.29 kg/tree and 33.99 kg/tree, respectively under D1 diameter class.  This increased production of biomass and storage of carbon can be explained by the increased absorption of light, water and nutrients by the large trees. Our findings corroborate with results of Wagay11 in Populus deltoides and Wani et al17 in Ulmus wallichiana.

The biomass allocation coefficients of branch and root (BACb and BACr) attained higher values in lower diameter classes (Table-4). The maximum and minimum values of these coefficients were 0.158 and 0.085; 0.298 and 0.278, respectively under D1 and D4 diameter classes. This trend can be explained by the increase in the stem biomass increment from lower diameter to higher diameter classes. The size of trees did not produce significant effect on the biomass allocation coefficient of foliage (BACf). This insignificant difference can be ascribed to higher foliage increments in the large trees.  Irrespective of size of the trees, the biomass allocation coefficients followed the order BACr > BACb > BACf. Wagay11 also found more allocation of biomass in roots as compared to branches and leaves in Populus deltoides. Moreover, Pathak et al18 and Sharma et al19 reported variation in biomass allocation to different components in some species of bamboo.

Table 4: Biomass allocation coefficients and growth efficiency of different tree components of 22- year old Ulmus wallichiana in different diameter classes

Diameter class (cm)

BACb

BACf

BACr

GEs

GEb

GEr

D1 (5-10)

0.158

0.040

0.298

1.261

0.192

0.373

D2 (10-15)

0.127

0.035

0.289

1.416

0.178

0.408

D3 (15-20)

0.138

0.043

0.295

1.134

0.149

0.332

D4 (>20)

0.085

0.030

0.278

2.084

0.158

0.572

Mean

0.127

0.037

0.290

1.473

0.169

0.421

CD (0.05)

0.032

NS

0.010

NS

NS

NS

 

BACb, BACf and BACr = Biomass allocation coefficients of branches, foliage and roots
GEs, GEb and GEr = Growth efficiency of stem, branches and roots.

The diameter of the trees produced insignificant difference in the growth efficiency (GE) of different tree components (Table-4). Kaufman and Ryan20 pointed out that suppressed and overtopped trees can reach GE values almost as high as the dominant individuals, mainly because they tend to maintain smaller mass of foliage relative to the stem. Irrespective of the diameter class, the highest growth efficiency was observed in stem (1.473) followed by roots (0.421) and branches (0.169). This trend can be attributed to more allocation of biomass in stem followed by roots and branches.

Conclusion

Biomass per tree of all tree components viz., stem, branches, foliage and roots showed significant difference among different diameter classes. The average values of these variables were highest in diameter class D4 (>20cm) and lowest in D1 (5-10cm).

Carbon stock and CO2e increased from lower to higher diameter classes.

Irrespective of size of the trees, the biomass allocation coefficients followed the order BACr > BACb > BACf.

The diameter of the trees produced insignificant difference in the growth efficiency (GE) of different tree components. However, the highest growth efficiency was observed in stem followed by roots and branches.


Acknowledgement

The authors greatfully acknowledge the support of the Faculty of Forestry, SKUAST-K during the course of investigation.

References
 

  1. Phartyal, S., Thapliyal, J., Nayal, J., & Joshi, G., Seed storage physiology of Himalayan Elm (Ulmus wallichiana): An endangered tree species. Seed Science and Technology, Vol. 31, International Seed Testing Association, Bassersdorf, Switzerland (2003).
  2. Canadell, J.G., Kirschbaum, M.U.F., Kurz, W.A., Sanz, M.J., Schlamadinger, B., & Yamagata, Y., Factoring out natural and indirect human effects on terrestrial carbon sources and sinks. Environmental Science and Policy, 10: 370-384 (2007).
    CrossRef
  3. , Global Forest Resources Assessment. FAO Forestry Paper 163. Rome (2010).
  4. Updegraff, K., Baughman, M.J., & Taff, S.J., Environmental benefits of cropland conversion to hybrid poplar: economic and policy considerations. Biomass Bioenergy, 27: 411-428 (2004).
    CrossRef
  5. , Transforming lives and landscapes through agroforestry science (Medium Term Plan 2010–2012). Nairobi, Kenya: World Agroforestry Centre (2009).
  6. , Task force on national greenhouse gas inventories. In: IPCC Guidelines for National Greenhouse Gas Inventories. (Eds. H.S. Eggleston, L. Buendia, K. Miwa, T. Ngara and K. Tanabe). IGES, Japan pp. 4.1-4.83 (2006).
  7. Bohre, P., Chaubey, O.P., & Singhal, P.K., Biomass accumulation and carbon sequestration in Tectona grandis f. and Gmelina arborea Roxb. International Journal of Bio-Science and Bio-Technology, 5(3): 153-174 (2013).
  8. Arifin, A., Tanaka, S., Jusop, S., Majid, N.M., Ibrahim, Z., Wasli, M.E., & Sakuri, K., Assessment on soil fertility status and growth performance of planted Dipterocarp species in peninsular Malaysia. Journal of Applied Science, 8: 3795-3805 (2008).
    CrossRef
  9. Yeboah, D., Burton, A. J., Storer, A.J., & Frimpong, E.O., Variation in wood density and carbon content of tropical plantation tree species from Ghana. New Forests, 45: 35-52 (2014).
    CrossRef
  10. Islam, M.A., & Masoodi, N.A., Growth performance and biomass productivity of a 9-year old Elm (Ulmus wallichiana) stand in Kashmir valley. SKUAST Journal of Research,  9: 191-197 (2007).
  11. Wagay, S.A., Biomass production, soil nutrient status and construction of volume table of poplar (Populus deltoides, Bartr.) plantation under rain fed conditions. Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir p. 59 (2012).
  12. Mitra, A., Sengupta, K., & Banerjee, K., Standing biomass and carbon storage of above-ground structures in dominant mangrove trees in Sundarbans. Forest Ecology and Management, 261(7): 1325-1335 (2011).
    CrossRef
  13. Pande, M.C., Tandon, V.N., & Rawat, H.S., Organic matter production and distribution of nutrients in Eucalyptus hybrid plantation ecosystems in Karnataka. Indian Forester, 113(11): 713-724 (1987).
  14. Singh, S.P., Adhikari, B.S., & Zobel, D.B., Biomass productivity, leaf longevity and plant structures in central Himalayas. Ecological Monographs, 64(4): 40-421 (1994).
    CrossRef
  15. Saralach, S.H., Nutrient dynamics and biomass production potential of Eucalyptus tereticornis Smith in high density short rotation systems. M.Sc. Thesis, Dr. Y.S. Parmar University of Horticulture and Forestry. Solan (H.P.) p. 99 (1994).
  16. Morhart, C., Sheppard, J., & Spiecker, H., Above ground leafless woody biomass and nutrient content within different compartments of a maximowicii × P. trichocarpa Poplar clone. Forests, 4: 471-487 (2013).
    CrossRef
  17. Wani, N.R., Qaisar, K.N., & Khan, P.A., Biomass and carbon allocation in different components of Ulmus wallichiana (elm): an endangered tree species of Kashmir valley. International Journal of Pharma and Bio Sciences, 5(1): (B) 860-872 (2014).
  18. Pathak, P.K., Kumar, H., Kumari, G., & Bilyaminu, H., Biomass production potential in different species of bamboo in Central Uttar Pradesh. The Ecoscan, 10(1): 41-43 (2015).
  19. Sharma, A., Shahi, C., Bargali, K., Bargali, S.S., & Rawat, Y.S., Biomass and carbon stock of Drepanostachyum falcatum (Nees) associated with oak forests at and around Nainital. The Ecoscan, 8(1&2): 105-108 (2014).
  20. Kaufmann, M.R., & Ryan, M.G., Physiographic, stand, and environmental effects on individual tree growth and growth efficiency in subalpine forests. Tree Physiology, 2: 47-59 (1986).
    CrossRef