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International Journal of Trend in Scientific Research and Development (IJTSRD)
Volume 7 Issue 1, January-February 2023 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470
@ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1217
Assessment of Biomass Content and Oxygen
Production from Tree of Subtropical Area
Dr. Mahima Chaurasia1
, Er. Nidhi Prasad2
, Dr. Sanjeev Kumar Srivastava3
, Dr. Siddhartha Shukla4
1, 3, 4
Dr. Rammanohar Lohia Avadh University, Ayodhya, Uttar Pradesh, India
2
I.E.T., Dr. Rammanohar Lohia Avadh University, Ayodhya, Uttar Pradesh, India
ABSTRACT
The accurate classification of tree species is critical for the
management of forest ecosystems, particularly subtropical forests,
which are highly diverse and complex ecosystems. While airborne
Light Detection and Ranging (LiDAR) technology offers significant
potential to estimate forest structural attributes, the capacity of this
new tool to classify species is less well known. In this research, full-
waveform metrics were extracted by a voxel-based composite
waveform approach and examined with a Random Forests classifier
to discriminate six subtropical tree species (i.e., Masson pine (Pinus
massoniana Lamb.)), Chinese fir (Cunninghamia lanceolata (Lamb.)
Hook.), Slash pines (Pinus elliottii Engelm.), Sawtooth oak (Quercus
acutissima Carruth.) and Chinese holly (Ilex chinensis Sims.) at three
levels of discrimination. As part of the analysis, the optimal voxel
size for modelling the composite waveforms was investigated, the
most important predictor metrics for species classification assessed
and the effect of scan angle on species discrimination examined.
Results demonstrate that all tree species were classified with
relatively high accuracy (68.6% for six classes, 75.8% for four main
species and 86.2% for conifers and broadleaved trees). Full-
waveform metrics (based on height of median energy, waveform
distance and number of waveform peaks) demonstrated high
classification importance and were stable among various voxel sizes.
The results also suggest that the voxel based approach can alleviate
some of the issues associated with large scan angles.
KEYWORDS: tree, subtropical, biomass, oxygen, classification,
median, sizes, species
How to cite this paper: Dr. Mahima
Chaurasia | Er. Nidhi Prasad | Dr.
Sanjeev Kumar Srivastava | Dr.
Siddhartha Shukla "Assessment of
Biomass Content and Oxygen
Production from Tree of Subtropical
Area" Published in
International
Journal of Trend in
Scientific Research
and Development
(ijtsrd), ISSN:
2456-6470,
Volume-7 | Issue-1,
February 2023, pp.1217-1221, URL:
www.ijtsrd.com/papers/ijtsrd53842.pdf
Copyright © 2023 by author (s) and
International Journal of Trend in
Scientific Research and Development
Journal. This is an
Open Access article
distributed under the
terms of the Creative Commons
Attribution License (CC BY 4.0)
(http://creativecommons.org/licenses/by/4.0)
INTRODUCTION
The impact of hydrologic regime shifts in the Asian
Monsoon under changing global climate is
significant, since the intensity of monsoon directly
affects the agricultural production of the most densely
populated regions in the world1
. Proxy climate
records dating back to the pre-instrumental era are
therefore essential for evaluating the roles of natural
variability and anthropogenic impact on the Asian
Monsoon system. Tree rings have often been used to
reconstruct past climate variations with annual
resolution, and extensive networks of tree-ring
chronologies have been developed in North America
and Europe. Unlike in higher latitudes, relatively few
tree-ring chronologies were produced for tropical and
subtropical Asia, since the lack of climatic seasonality
hinders annual ring formation of most tree species in
these regions. However, over the last couple of
decades dendrochronologists2
have found increasing
success in the low latitudes of Asia by selecting
regions with more pronounced temperature or
precipitation seasonality. A major recent advance has
been the hydroclimatic reconstructions from rare and
long-lived Fujian Cypress (Fokienia hodginsii)
growing in Vietnam (Buckley et al. 2010; Sano et al.
2009). These records based on ring width
measurement revealed that the region experienced
decadal-scale droughts in the past, which have no
analog in the instrumental period. 3
Interestingly,
these exceptional droughts coincided with periods of
social unrest (Buckley et al. 2010). In addition to this
progress, other recent studies indicated that oxygen
isotope ratios of tree-ring cellulose might help
IJTSRD53842
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1218
improve our understanding of monsoon activity (Sano
et al. 2012a,b ; Xu et al. 2011). In this brief note, we
show some advantages of using tree-ring δ18O rather
than ring width and wood density traditionally
utilized in dendroclimatolgy.
It is well known that tree-ring width and wood
density are controlled not only by climate but also by
endogenous disturbance pulses, such as competition
with neighboring trees. To reduce such disturbances,
climatically sensitive trees are sampled
predominantly at the species ecological boundaries,
such as near arid or cold forest limits. This spatial
limitation can be overcome by using oxygen isotope
ratios,4
since the isotopic ratio in the wood is not
significantly affected by ecophysiological processes.
Tree-ring δ18O is theoretically controlled by two
climatic factors, δ18O of the source water and relative
humidity (e.g. Robertson et al. 2001; Saurer et al.
1997), both of which are closely related to monsoon
activity in South and Southeast Asia. Our preliminary
analyses using samples from the Himalayas (Sano et
al. 2010) and Laos (Xu et al. 2011) clearly show that
tree-ring δ18O is more strongly correlated with
precipitation, relative humidity, temperature and
Palmer Drought Severity Index (PDSI) than is ring
width or wood density. PDSI is a drought metric
based upon a water balance model. Positive and
negative values of the PDSI correspond respectively
to wet and dry conditions (Palmer 1965; Dai et al.
2004). Tree-ring δ18O from the Nepal Himalayas
accounts for 34% of the inter-annual variability of the
PDSI in the monsoon season (July–September), and
clearly shows a decreasing trend of
precipitation/moisture over the last two centuries.
Evidence for a decrease in summer monsoon rainfall
was also found in δ18O of tree rings from Tibet
(Grießinger et al. 2011), δD of an ice core from Mt.
Everest (Kaspari et al. 2007), snow accumulation of
an ice core from Dasuopu, Tibet (Zhao and Moore
2006), and varve thickness of lake sediments in Tibet
(Chu et al. 2011). The overall trends toward arid
conditions indicate that summer monsoon has
weakened across wide areas of the Himalayas and
Tibet for at least the last couple of centuries.5
Our reconstructed PDSI shows significant
correlations with sea surface temperatures in the
tropical Pacific and Indian Ocean, suggesting that the
tropical oceans play a role in modulating
hydroclimate in the Nepal Himalayas. A simulation
model forced by observed sea surface temperature
(SST) data reveals that a weakening trend of monsoon
precipitation found in northern India and the eastern
Tibetan Plateau over the latter half of the 20th century
is deducible from the atmosphere’s response to an
increase in SSTs over the tropical Pacific and Indian
Ocean (Zhou et al. 2008). Therefore, the consistent
warming found in reconstruction of tropical SSTs
over the last two centuries (Wilson et al. 2006) might
be responsible for the weakening monsoon in the
Himalayas.6
In contrast, other proxy records from
lower altitudes indicate a strengthening of the
monsoon winds (Anderson et al. 2002) and
precipitation (Wang et al. 2005). The increased
north–south difference of monsoon activity is likely
induced by a southward shift in the overall position of
the monsoon trough. In contrast to ring-width-based
reconstructions from the Himalayas and Tibet, those
from Southeast Asia are rare, since most trees grow in
relatively warm and wet environments.7
To overcome
this limitation, isotopic analyses have been conducted
on samples from four cypress trees from Laos for the
past 52 years (1951-2002). It turned out that contrary
to the tree-ring widths data (Xu et al. 2011), the δ18O
time series of the trees are significantly correlated
with each other. Also, the δ18O chronology built
from the four trees shows significant correlation with
temperature (r = 0.64, p < 0.001), precipitation (r = –
0.34, p < 0.05) and PDSI (r = –0.66, p < 0.001) in the
monsoon season. In contrast, no significant
correlation was found between any climatic variables
and a ring-width chronology based on 15 trees, which
includes the four trees utilized for the isotope
measurement. Finally, the δ18O chronology is
strongly correlated with ENSO-related indices,
particularly with the Multivariate ENSO Index (MEI;
Wolter and Timlin 2011) for the last 52 years. To
further explore the potential of isotope
dendroclimatology, six more cypress trees from
Vietnam have been subjected to δ18O analyses.
Surprisingly, the δ18O chronology from Vietnam is
closely correlated to that from Laos (Sano et al.
2012b), even though these sampling sites are around
150 km away from each other. Moreover, the
teleconnected relationships between the δ18O
chronology and ENSO-related indices are stable over
the 135-year period of available instrumental data.8
Over the last decade, considerable effort has been
devoted to reconstruct ENSO variability using tree
rings and other proxy records that originate mainly
from North America and the topical Pacific (e.g.
D'Arrigo et al. 2005; Mann et al. 2000; Wilson et al.
2010). Although these records agree well during the
twentieth century, there is relatively little agreement
before this time. Wilson et al. (2010) point out that
the teleconnected relationship between the tropical
central/eastern Pacific and regions where proxy
records are located does not seem to be stable. Since
none of the previously published reconstructions of
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1219
ENSO variability include data from mainland
Southeast Asia, tree-ring δ18O is of great use to
independently reconstruct ENSO, and to explore the
spatial influence of ENSO before the instrumental
period.9
Discussion
Forests are the world's largest carbon sink and play a
vital role in climate change mitigation through carbon
sequestration; thus the assessment of carbon stock in
the forests is important for policy prescription and
management planning. In view of this, present study
is an attempt to assess the biomass and carbon stock
of tree species in selected subtropical and temperate
forest stands along the vertical elevation gradient
(300 m to 2250 m) in the Central Himalaya.
Volumetric equations (allometric method) were used
for various tree species along with field sampling/
assessment (quadrat method) for biomass and carbon
sequestration potentials. The total tree biomass and
carbon stock of dominant forest stands varied from
227.23 to 577.16 Mg ha−1 (megagram per hectare),
and 107.93 to 274.15 Mg C ha−1 respectively; it was
found maximum for Sal (Shorea robusta) dominated
forest and minimum for mixed Oak forest (Quercus
floribunda, Q. lanuginosa, Q. leucotrichophora etc.).
The carbon sequestration was recorded maximum
(4.83 Mg C ha−1 yr−1) for Chir-pine stand (Pinus
roxburghii) followed by Sal (4.63 Mg C ha−1 yr−1),
mixed Oak (4.47 Mg C ha−1 yr−1), and minimum
(3.99 Mg C ha−1 yr−1) for temperate Banj-oak forest
(Quercus leucotrichophora). The contribution of
above and below ground biomass among different
forest stands was recorded 82% and 18%
respectively. The dominant species contributed
maximum biomass and carbon stock (70–82%) in
pure Sal, Chir-pine and Banj-oak stand, while the
contribution of dominant and co-dominant species in
the mixed forest varied depending on forest
composition.10
The results reveal higher carbon stock
for subtropical forest as compared to temperate forest;
however, it is interesting that there is no significant
difference in carbon sequestration among the different
forest stands. The study recommended for the
assessing biomass and carbon stock of different
forests for long-term management of forests and
climate change mitigation.11
Tree biomass and species diversity have a key role in
regulating proper ecosystem functioning. The present
study explored variability among four Sal (Shorea
robusta Gaertn. f.) forest stands of Bhabar belt of
Nainital district of Uttarakhand, Central Himalaya
within an elevational range of 405–575 m. Quadrat
method was used for sampling to assess the
phytosociology and allometric regression equations
for biomass and carbon stocks. Significant differences
were observed among forest stands in terms of
structural attributes. The study sites catalogued 26
tree species with highest species richness on site
Ranibagh (RB). Tree density ranged in between 620
individuals ha− 1 [site Fatehpur (FP)] and 810
individuals ha− 1 (site RB). The Kaladhungi (KD)
site yielded maximum biomass (317.60 Mg ha− 1)
followed by site FP (274.05 Mg ha− 1), site RB
(248.62 Mg ha− 1) and least (221.46 Mg ha− 1) by
site AP (Amritpur). The maximum carbon stock
(244.82 Mg C ha− 1) was recorded on site AP,
followed by site KD (150.86 Mg C ha− 1), site FP
(130.18 Mg C ha− 1) and site RB (116.91 Mg C
ha− 1). The maximum biomass and carbon stock
(61.09–92.23%) was endowed by dominant tree
species (S. robusta). The aboveground components
among forest stands contributed 71.84–77.23%, while
belowground biomass contributed 26.76–27.24% to
the total biomass. The sub-tropical forests across
Central Himalayan regions have been modified by
biotic interferences that alter the ecosystem structural
and functional aspects including plant diversity,
nutrient cycling and productive traits. Thus, assessing
the variability in phyto-sociological parameters of
forests is important for planning well- structured and
precise forest management regimes.12
Results
Forest ecosystems are an integral component of the
global carbon cycle as they take up and release large
amounts of Cover short time periods (C flux) or
accumulate it over longer time periods (C stock).
However, there remains uncertainty about whether
and in which direction C fluxes and in particular C
stocks may differ between forests of high versus low
species richness. Based on a comprehensive dataset
derived from field-based measurements, we tested the
effect of species richness (3–20 tree species) and
stand age (22–116 years) on six compartments of
above- and below-ground C stocks and four
components of C fluxes in subtropical forests in
southeast China. Across forest stands, total C stock
was 149 ± 12 Mg ha−1
with richness explaining
28.5% and age explaining 29.4% of variation in this
measure. Species-rich stands had higher C stocks and
fluxes than stands with low richness; and, in addition,
old stands had higher C stocks than young ones.13
Overall, for each additional tree species, the total C
stock increased by 6.4%. Our results provide
comprehensive evidence for diversity-mediated
above- and below-ground C sequestration in species-
rich subtropical forests in southeast China. Therefore,
afforestation policies in this region and elsewhere
should consider a change from the current focus on
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1220
monocultures to multi-species plantations to increase
C fixation and thus slow increasing atmospheric CO2
concentrations and global warming. Previous
biodiversity–productivity studies in forest ecosystems
reported positive effects of tree species richness on
above-ground components of primary productivity,
suggesting that more C might be stored in species-
rich forests. We found more C below than above
ground in our subtropical forests, raising the question
whether richness effects might be changed if total
rather than only above-ground C storage is
considered. Our findings demonstrate that indeed
total above- and below-ground C storage in
subtropical forest increases with species richness if
major components of C fluxes and C stocks are
considered. At the regional scale, subtropical forests
in southeast China are a major potential C sink
because of the implementation of large afforestation
and plantation programmes in the last 36 years.
However, these plantations were mainly established
with single species and even though they will
continue to accumulate C if their continued growth
can be maintained into the future, much larger
amounts of C could have been stored according to our
study if plantation programmes would have adopted
multi-species planting schemes.14
Conclusions
Assuming a total amount of 30.3 Tg C stored per year
by the planted monoculture forests in China
tentatively valued at 0.4 billion dollar, and
extrapolating our results to other types of forests, an
additional 6.4% C ha−1
could have been stored per
year for every additional species. As a consequence,
amounts in the order of 0.3 billion dollars per year
(0.4 × 0.0649
) might have been gained by using 10-
species mixtures instead of monocultures for the 0.89
× 106
ha of planted forests in China. This assumes
that the relationship between monocultures and 10-
species mixtures has a similar slope to the one we
found here between three- and 20-species mixtures.
At the same time, this indicates the potential gains
that could still be realized by switching to species-
rich plantation schemes now. Such plantation
schemes may be costly to carry out but could have the
additional advantage that species-rich forests can be
expected to be more stable and resistant to global
change and to extreme events, and they contribute to
biodiversity maintenance. Therefore, biodiversity
should be considered as an integral component in
forest-carbon management strategies.15
References
[1] This article incorporates text available under
the CC BY-SA 3.0 license. World Wide Fund
for Nature. "Tropical and Subtropical Dry
Broadleaf Forest Ecoregions". Archived from
the original on 2012-04-25. Retrieved 2012-09-
25.
[2] Gentry, A (1993). "Diversity and floristic
composition of Neotropical dry forests". In
Mooney, H; Bullock, S; Medina, E (eds.).
Tropical deciduous forest ecosystems.
Cambridge, UK: Cambridge University Press.
pp. 146–194.
[3] Mongbay: Types of tropical forest (accessed 21
March 2017)
[4] Beard, J.S.; Keneally, K.F. (1987), 'Rainforests
of Western Australia'. In 'The rainforest legacy:
Australian national rainforests study'. Special
Australian heritage publication series 7(1), pp.
289–304
[5] Webb, L. J. (Leonard James); Tracey, J. G.
(John Geoffrey) (1982), An ecological survey
of the monsoon forests of the north-western
region of the Northern Territory, Australian
National Parks and Wildlife Service
[6] Russell-Smith, Jeremy; Dunlop, Clyde (1987),
The status of monsoon vine forests in the
Northern Territory: a perspective. In 'The
rainforest legacy: Australian national
rainforests study. Special Australian heritage
publication series 7(1)
[7] Stanton, J.P.; Fell, David. G. (2005). "The
rainforests of Cape York Peninsula". Rainforest
CRC – via National Library of Australia.
[8] Leigh EG, Rand AS, Windsor DM (Eds. 1983)
The ecology of a tropical forest. Seasonal
rhythms and long-term changes. Oxford
University Press 468 pp.
[9] NWS JetStream – Inter-Tropical Convergence
Zone. Srh.noaa.gov (5 January2010). Retrieved
on 28 March 2013.
[10] Malhi, Yadvinder & Wright, James (2004).
"Spatial patterns and recent trends in the
climate of tropical rainforest regions".
Philosophical Transactions of the Royal Society
of London. Series B: Biological Sciences. 359
(1443): 311–329. doi:10.1098/rstb.2003.1433.
PMC 1693325. PMID 15212087.
[11] Ya-Jun Chen, Kun-Fang Cao, Stefan A.
Schnitzer, Ze-Xin Fan, Jiao-Lin Zhang, Frans
Bongers (2015) Water-use advantage of lianas
over trees in seasonal tropical forests. New
Phytologist, 205[1]: 128–136
International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1221
[12] Buckley BM et al. (2010) PNAS 107: 6748-
6752
[13] Sano M, Ramesh R, Sheshshayee MS, Sukumar
R (2012a) The Holocene 22(7): 809-817
[14] Sano M, Xu C and Nakatsuka T (2012b)
Journal of Geophysical Research 117,
doi:10.1029/2012JD017749
[15] Wilson R et al. (2010) Journal of Quaternary
Science 25(1): 62-78
[16] Xu C, Sano M, Nakatsuka T (2011) Journal of
Geophysical Research 116,
doi:10.1029/2011JD016694

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Assessment of Biomass Content and Oxygen Production from Tree of Subtropical Area

  • 1. International Journal of Trend in Scientific Research and Development (IJTSRD) Volume 7 Issue 1, January-February 2023 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470 @ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1217 Assessment of Biomass Content and Oxygen Production from Tree of Subtropical Area Dr. Mahima Chaurasia1 , Er. Nidhi Prasad2 , Dr. Sanjeev Kumar Srivastava3 , Dr. Siddhartha Shukla4 1, 3, 4 Dr. Rammanohar Lohia Avadh University, Ayodhya, Uttar Pradesh, India 2 I.E.T., Dr. Rammanohar Lohia Avadh University, Ayodhya, Uttar Pradesh, India ABSTRACT The accurate classification of tree species is critical for the management of forest ecosystems, particularly subtropical forests, which are highly diverse and complex ecosystems. While airborne Light Detection and Ranging (LiDAR) technology offers significant potential to estimate forest structural attributes, the capacity of this new tool to classify species is less well known. In this research, full- waveform metrics were extracted by a voxel-based composite waveform approach and examined with a Random Forests classifier to discriminate six subtropical tree species (i.e., Masson pine (Pinus massoniana Lamb.)), Chinese fir (Cunninghamia lanceolata (Lamb.) Hook.), Slash pines (Pinus elliottii Engelm.), Sawtooth oak (Quercus acutissima Carruth.) and Chinese holly (Ilex chinensis Sims.) at three levels of discrimination. As part of the analysis, the optimal voxel size for modelling the composite waveforms was investigated, the most important predictor metrics for species classification assessed and the effect of scan angle on species discrimination examined. Results demonstrate that all tree species were classified with relatively high accuracy (68.6% for six classes, 75.8% for four main species and 86.2% for conifers and broadleaved trees). Full- waveform metrics (based on height of median energy, waveform distance and number of waveform peaks) demonstrated high classification importance and were stable among various voxel sizes. The results also suggest that the voxel based approach can alleviate some of the issues associated with large scan angles. KEYWORDS: tree, subtropical, biomass, oxygen, classification, median, sizes, species How to cite this paper: Dr. Mahima Chaurasia | Er. Nidhi Prasad | Dr. Sanjeev Kumar Srivastava | Dr. Siddhartha Shukla "Assessment of Biomass Content and Oxygen Production from Tree of Subtropical Area" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-7 | Issue-1, February 2023, pp.1217-1221, URL: www.ijtsrd.com/papers/ijtsrd53842.pdf Copyright © 2023 by author (s) and International Journal of Trend in Scientific Research and Development Journal. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0) INTRODUCTION The impact of hydrologic regime shifts in the Asian Monsoon under changing global climate is significant, since the intensity of monsoon directly affects the agricultural production of the most densely populated regions in the world1 . Proxy climate records dating back to the pre-instrumental era are therefore essential for evaluating the roles of natural variability and anthropogenic impact on the Asian Monsoon system. Tree rings have often been used to reconstruct past climate variations with annual resolution, and extensive networks of tree-ring chronologies have been developed in North America and Europe. Unlike in higher latitudes, relatively few tree-ring chronologies were produced for tropical and subtropical Asia, since the lack of climatic seasonality hinders annual ring formation of most tree species in these regions. However, over the last couple of decades dendrochronologists2 have found increasing success in the low latitudes of Asia by selecting regions with more pronounced temperature or precipitation seasonality. A major recent advance has been the hydroclimatic reconstructions from rare and long-lived Fujian Cypress (Fokienia hodginsii) growing in Vietnam (Buckley et al. 2010; Sano et al. 2009). These records based on ring width measurement revealed that the region experienced decadal-scale droughts in the past, which have no analog in the instrumental period. 3 Interestingly, these exceptional droughts coincided with periods of social unrest (Buckley et al. 2010). In addition to this progress, other recent studies indicated that oxygen isotope ratios of tree-ring cellulose might help IJTSRD53842
  • 2. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1218 improve our understanding of monsoon activity (Sano et al. 2012a,b ; Xu et al. 2011). In this brief note, we show some advantages of using tree-ring δ18O rather than ring width and wood density traditionally utilized in dendroclimatolgy. It is well known that tree-ring width and wood density are controlled not only by climate but also by endogenous disturbance pulses, such as competition with neighboring trees. To reduce such disturbances, climatically sensitive trees are sampled predominantly at the species ecological boundaries, such as near arid or cold forest limits. This spatial limitation can be overcome by using oxygen isotope ratios,4 since the isotopic ratio in the wood is not significantly affected by ecophysiological processes. Tree-ring δ18O is theoretically controlled by two climatic factors, δ18O of the source water and relative humidity (e.g. Robertson et al. 2001; Saurer et al. 1997), both of which are closely related to monsoon activity in South and Southeast Asia. Our preliminary analyses using samples from the Himalayas (Sano et al. 2010) and Laos (Xu et al. 2011) clearly show that tree-ring δ18O is more strongly correlated with precipitation, relative humidity, temperature and Palmer Drought Severity Index (PDSI) than is ring width or wood density. PDSI is a drought metric based upon a water balance model. Positive and negative values of the PDSI correspond respectively to wet and dry conditions (Palmer 1965; Dai et al. 2004). Tree-ring δ18O from the Nepal Himalayas accounts for 34% of the inter-annual variability of the PDSI in the monsoon season (July–September), and clearly shows a decreasing trend of precipitation/moisture over the last two centuries. Evidence for a decrease in summer monsoon rainfall was also found in δ18O of tree rings from Tibet (Grießinger et al. 2011), δD of an ice core from Mt. Everest (Kaspari et al. 2007), snow accumulation of an ice core from Dasuopu, Tibet (Zhao and Moore 2006), and varve thickness of lake sediments in Tibet (Chu et al. 2011). The overall trends toward arid conditions indicate that summer monsoon has weakened across wide areas of the Himalayas and Tibet for at least the last couple of centuries.5 Our reconstructed PDSI shows significant correlations with sea surface temperatures in the tropical Pacific and Indian Ocean, suggesting that the tropical oceans play a role in modulating hydroclimate in the Nepal Himalayas. A simulation model forced by observed sea surface temperature (SST) data reveals that a weakening trend of monsoon precipitation found in northern India and the eastern Tibetan Plateau over the latter half of the 20th century is deducible from the atmosphere’s response to an increase in SSTs over the tropical Pacific and Indian Ocean (Zhou et al. 2008). Therefore, the consistent warming found in reconstruction of tropical SSTs over the last two centuries (Wilson et al. 2006) might be responsible for the weakening monsoon in the Himalayas.6 In contrast, other proxy records from lower altitudes indicate a strengthening of the monsoon winds (Anderson et al. 2002) and precipitation (Wang et al. 2005). The increased north–south difference of monsoon activity is likely induced by a southward shift in the overall position of the monsoon trough. In contrast to ring-width-based reconstructions from the Himalayas and Tibet, those from Southeast Asia are rare, since most trees grow in relatively warm and wet environments.7 To overcome this limitation, isotopic analyses have been conducted on samples from four cypress trees from Laos for the past 52 years (1951-2002). It turned out that contrary to the tree-ring widths data (Xu et al. 2011), the δ18O time series of the trees are significantly correlated with each other. Also, the δ18O chronology built from the four trees shows significant correlation with temperature (r = 0.64, p < 0.001), precipitation (r = – 0.34, p < 0.05) and PDSI (r = –0.66, p < 0.001) in the monsoon season. In contrast, no significant correlation was found between any climatic variables and a ring-width chronology based on 15 trees, which includes the four trees utilized for the isotope measurement. Finally, the δ18O chronology is strongly correlated with ENSO-related indices, particularly with the Multivariate ENSO Index (MEI; Wolter and Timlin 2011) for the last 52 years. To further explore the potential of isotope dendroclimatology, six more cypress trees from Vietnam have been subjected to δ18O analyses. Surprisingly, the δ18O chronology from Vietnam is closely correlated to that from Laos (Sano et al. 2012b), even though these sampling sites are around 150 km away from each other. Moreover, the teleconnected relationships between the δ18O chronology and ENSO-related indices are stable over the 135-year period of available instrumental data.8 Over the last decade, considerable effort has been devoted to reconstruct ENSO variability using tree rings and other proxy records that originate mainly from North America and the topical Pacific (e.g. D'Arrigo et al. 2005; Mann et al. 2000; Wilson et al. 2010). Although these records agree well during the twentieth century, there is relatively little agreement before this time. Wilson et al. (2010) point out that the teleconnected relationship between the tropical central/eastern Pacific and regions where proxy records are located does not seem to be stable. Since none of the previously published reconstructions of
  • 3. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1219 ENSO variability include data from mainland Southeast Asia, tree-ring δ18O is of great use to independently reconstruct ENSO, and to explore the spatial influence of ENSO before the instrumental period.9 Discussion Forests are the world's largest carbon sink and play a vital role in climate change mitigation through carbon sequestration; thus the assessment of carbon stock in the forests is important for policy prescription and management planning. In view of this, present study is an attempt to assess the biomass and carbon stock of tree species in selected subtropical and temperate forest stands along the vertical elevation gradient (300 m to 2250 m) in the Central Himalaya. Volumetric equations (allometric method) were used for various tree species along with field sampling/ assessment (quadrat method) for biomass and carbon sequestration potentials. The total tree biomass and carbon stock of dominant forest stands varied from 227.23 to 577.16 Mg ha−1 (megagram per hectare), and 107.93 to 274.15 Mg C ha−1 respectively; it was found maximum for Sal (Shorea robusta) dominated forest and minimum for mixed Oak forest (Quercus floribunda, Q. lanuginosa, Q. leucotrichophora etc.). The carbon sequestration was recorded maximum (4.83 Mg C ha−1 yr−1) for Chir-pine stand (Pinus roxburghii) followed by Sal (4.63 Mg C ha−1 yr−1), mixed Oak (4.47 Mg C ha−1 yr−1), and minimum (3.99 Mg C ha−1 yr−1) for temperate Banj-oak forest (Quercus leucotrichophora). The contribution of above and below ground biomass among different forest stands was recorded 82% and 18% respectively. The dominant species contributed maximum biomass and carbon stock (70–82%) in pure Sal, Chir-pine and Banj-oak stand, while the contribution of dominant and co-dominant species in the mixed forest varied depending on forest composition.10 The results reveal higher carbon stock for subtropical forest as compared to temperate forest; however, it is interesting that there is no significant difference in carbon sequestration among the different forest stands. The study recommended for the assessing biomass and carbon stock of different forests for long-term management of forests and climate change mitigation.11 Tree biomass and species diversity have a key role in regulating proper ecosystem functioning. The present study explored variability among four Sal (Shorea robusta Gaertn. f.) forest stands of Bhabar belt of Nainital district of Uttarakhand, Central Himalaya within an elevational range of 405–575 m. Quadrat method was used for sampling to assess the phytosociology and allometric regression equations for biomass and carbon stocks. Significant differences were observed among forest stands in terms of structural attributes. The study sites catalogued 26 tree species with highest species richness on site Ranibagh (RB). Tree density ranged in between 620 individuals ha− 1 [site Fatehpur (FP)] and 810 individuals ha− 1 (site RB). The Kaladhungi (KD) site yielded maximum biomass (317.60 Mg ha− 1) followed by site FP (274.05 Mg ha− 1), site RB (248.62 Mg ha− 1) and least (221.46 Mg ha− 1) by site AP (Amritpur). The maximum carbon stock (244.82 Mg C ha− 1) was recorded on site AP, followed by site KD (150.86 Mg C ha− 1), site FP (130.18 Mg C ha− 1) and site RB (116.91 Mg C ha− 1). The maximum biomass and carbon stock (61.09–92.23%) was endowed by dominant tree species (S. robusta). The aboveground components among forest stands contributed 71.84–77.23%, while belowground biomass contributed 26.76–27.24% to the total biomass. The sub-tropical forests across Central Himalayan regions have been modified by biotic interferences that alter the ecosystem structural and functional aspects including plant diversity, nutrient cycling and productive traits. Thus, assessing the variability in phyto-sociological parameters of forests is important for planning well- structured and precise forest management regimes.12 Results Forest ecosystems are an integral component of the global carbon cycle as they take up and release large amounts of Cover short time periods (C flux) or accumulate it over longer time periods (C stock). However, there remains uncertainty about whether and in which direction C fluxes and in particular C stocks may differ between forests of high versus low species richness. Based on a comprehensive dataset derived from field-based measurements, we tested the effect of species richness (3–20 tree species) and stand age (22–116 years) on six compartments of above- and below-ground C stocks and four components of C fluxes in subtropical forests in southeast China. Across forest stands, total C stock was 149 ± 12 Mg ha−1 with richness explaining 28.5% and age explaining 29.4% of variation in this measure. Species-rich stands had higher C stocks and fluxes than stands with low richness; and, in addition, old stands had higher C stocks than young ones.13 Overall, for each additional tree species, the total C stock increased by 6.4%. Our results provide comprehensive evidence for diversity-mediated above- and below-ground C sequestration in species- rich subtropical forests in southeast China. Therefore, afforestation policies in this region and elsewhere should consider a change from the current focus on
  • 4. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1220 monocultures to multi-species plantations to increase C fixation and thus slow increasing atmospheric CO2 concentrations and global warming. Previous biodiversity–productivity studies in forest ecosystems reported positive effects of tree species richness on above-ground components of primary productivity, suggesting that more C might be stored in species- rich forests. We found more C below than above ground in our subtropical forests, raising the question whether richness effects might be changed if total rather than only above-ground C storage is considered. Our findings demonstrate that indeed total above- and below-ground C storage in subtropical forest increases with species richness if major components of C fluxes and C stocks are considered. At the regional scale, subtropical forests in southeast China are a major potential C sink because of the implementation of large afforestation and plantation programmes in the last 36 years. However, these plantations were mainly established with single species and even though they will continue to accumulate C if their continued growth can be maintained into the future, much larger amounts of C could have been stored according to our study if plantation programmes would have adopted multi-species planting schemes.14 Conclusions Assuming a total amount of 30.3 Tg C stored per year by the planted monoculture forests in China tentatively valued at 0.4 billion dollar, and extrapolating our results to other types of forests, an additional 6.4% C ha−1 could have been stored per year for every additional species. As a consequence, amounts in the order of 0.3 billion dollars per year (0.4 × 0.0649 ) might have been gained by using 10- species mixtures instead of monocultures for the 0.89 × 106 ha of planted forests in China. This assumes that the relationship between monocultures and 10- species mixtures has a similar slope to the one we found here between three- and 20-species mixtures. At the same time, this indicates the potential gains that could still be realized by switching to species- rich plantation schemes now. Such plantation schemes may be costly to carry out but could have the additional advantage that species-rich forests can be expected to be more stable and resistant to global change and to extreme events, and they contribute to biodiversity maintenance. Therefore, biodiversity should be considered as an integral component in forest-carbon management strategies.15 References [1] This article incorporates text available under the CC BY-SA 3.0 license. World Wide Fund for Nature. "Tropical and Subtropical Dry Broadleaf Forest Ecoregions". Archived from the original on 2012-04-25. Retrieved 2012-09- 25. [2] Gentry, A (1993). "Diversity and floristic composition of Neotropical dry forests". In Mooney, H; Bullock, S; Medina, E (eds.). Tropical deciduous forest ecosystems. Cambridge, UK: Cambridge University Press. pp. 146–194. [3] Mongbay: Types of tropical forest (accessed 21 March 2017) [4] Beard, J.S.; Keneally, K.F. (1987), 'Rainforests of Western Australia'. In 'The rainforest legacy: Australian national rainforests study'. Special Australian heritage publication series 7(1), pp. 289–304 [5] Webb, L. J. (Leonard James); Tracey, J. G. (John Geoffrey) (1982), An ecological survey of the monsoon forests of the north-western region of the Northern Territory, Australian National Parks and Wildlife Service [6] Russell-Smith, Jeremy; Dunlop, Clyde (1987), The status of monsoon vine forests in the Northern Territory: a perspective. In 'The rainforest legacy: Australian national rainforests study. Special Australian heritage publication series 7(1) [7] Stanton, J.P.; Fell, David. G. (2005). "The rainforests of Cape York Peninsula". Rainforest CRC – via National Library of Australia. [8] Leigh EG, Rand AS, Windsor DM (Eds. 1983) The ecology of a tropical forest. Seasonal rhythms and long-term changes. Oxford University Press 468 pp. [9] NWS JetStream – Inter-Tropical Convergence Zone. Srh.noaa.gov (5 January2010). Retrieved on 28 March 2013. [10] Malhi, Yadvinder & Wright, James (2004). "Spatial patterns and recent trends in the climate of tropical rainforest regions". Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences. 359 (1443): 311–329. doi:10.1098/rstb.2003.1433. PMC 1693325. PMID 15212087. [11] Ya-Jun Chen, Kun-Fang Cao, Stefan A. Schnitzer, Ze-Xin Fan, Jiao-Lin Zhang, Frans Bongers (2015) Water-use advantage of lianas over trees in seasonal tropical forests. New Phytologist, 205[1]: 128–136
  • 5. International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD53842 | Volume – 7 | Issue – 1 | January-February 2023 Page 1221 [12] Buckley BM et al. (2010) PNAS 107: 6748- 6752 [13] Sano M, Ramesh R, Sheshshayee MS, Sukumar R (2012a) The Holocene 22(7): 809-817 [14] Sano M, Xu C and Nakatsuka T (2012b) Journal of Geophysical Research 117, doi:10.1029/2012JD017749 [15] Wilson R et al. (2010) Journal of Quaternary Science 25(1): 62-78 [16] Xu C, Sano M, Nakatsuka T (2011) Journal of Geophysical Research 116, doi:10.1029/2011JD016694