• google scholor
  • Views: 83

  • PDF Downloads: 0

Assessment of Annual Litterfall of Woody Plant Community in Southern Thorn Forest, Tirunelveli, Peninsular India

Johnson Evitex-Izayas and Muthulingam Udayakumar *

1 Department of Plant Science, Manonmaniam Sundaranar University, Tirunelveli, Tamil Nadu India

Corresponding author Email: udayakumar@msuniv.ac.in

DOI: http://dx.doi.org/10.12944/CWE.19.2.27

The biological phenomenon, litterfall acts as a connection between tree canopy and substratum of the habitats, influencing the concentration of vital soil nutrients thereby contributing to the tree growth and forest productivity. Information on litter generation of tropical forests including tropical thorn forest is lacking. Therefore, the current study was conducted to find annual litterfall of tree community existing within a Reserve Forest in Tirunelveli, India. A field ecological study was carried out to find annual litter production of woody plant community. Litter traps were kept randomly across the forest to assess the litter production. The litter fallen in each trap was collected separately on monthly basis for one calendar year. The collected litter was separated in to four different classes viz., leaf, wood, amorphous and reproductive organs. The relationship of climatic variables with litterfall was estimated by Pearson’s simple correlation test. The annual litter generation of the study area was estimated at 8.058 tons ha-1 y-1. The amount of total fallen and four classes litter per month varied significantly. In addition, litterfall did not show any significant relationship with the mean monthly temperature (p = 0.128; r2= 0.216) and monthly rainfall (p = 0.817; r2 = 0.0056). The deciduous species accounted for 95% (3.449 tons ha-1) of total annual leaf litterfall. Among four litter classes, the leaf litter accounted for 45.05%. The quantity of annual litterfall recorded from present study area is comparable with other tropical dry forests. The present study concentrated on limited forest areas, further studies with larger study area are needed to quantify the actual annual litter generation of southern thorn forests flourishing in various districts of Tamil Nadu.

Climatic variables; Deciduous; Dry Forest; Leaf litterfall; Physiognomy

Copy the following to cite this article:

Izayas J. E, Udayakumar M. Assessment of Annual Litterfall of Woody Plant Community in Southern Thorn Forest, Tirunelveli, Peninsular India. Curr World Environ 2024;19(2). DOI:http://dx.doi.org/10.12944/CWE.19.2.27

Copy the following to cite this URL:

Izayas J. E, Udayakumar M. Assessment of Annual Litterfall of Woody Plant Community in Southern Thorn Forest, Tirunelveli, Peninsular India. Curr World Environ 2024;19(2).


Download article (pdf)
Citation Manager
Publish History


Article Publishing History

Received: 2023-11-27
Accepted: 2024-08-19
Reviewed by: Orcid Orcid Rania Khater
Second Review by: Orcid Orcid Prashant Sharma
Final Approval by: Dr Hemant Kumar

Introduction

The litterfall is one of the important events in forest ecosystem, it facilitates the return of vital nutrients and add significant amount of carbon (C) into the soil.1-4 Information on forest litterfall is important to understand the patterns and factors which influence litterfall across forest types.5 In addition, the litterfall offers energy and nutrients to detritivores, adds organic matter content to soil and provides essential growth nutrients to plants.3,6,7 The total litterfall consists leaf litter and non-leaf litter including reproductive organs, bark, twigs and amorphous or inseparable litter.8

The rate of degradation depends on an array of factors including chemical composition of leaves,9 C/N ratio,10 physiognomy11 and functional traits.12 It is well known that environmental factors including rainfall, temperature and length of the growing season, and characteristics of vegetation including community composition, density, basal area, and age influence litter production.13-16  Comparative studies on the total litter production showed that litter production of dry forests is lower than in wet tropical forests.14,17 The global terrestrial litter production has been estimated as 39 to 54 Gigaton (Gt) yr-1,18, 19 in which global forest litter production was 29 Gt yr-1.20 Notably, 13% of the world’s annual litterfall is constituted by tropical forests.21 In general, the amount of litterfall vary across forests, the litterfall in temperate, tropical rain and sub-tropical rain forests recorded as 3-5, 12 and 16 tons ha-1 yr-1, respectively.22 The mean annual litterfall of Indian tropical forests was estimated as 9.3 tons ha-1.23

Indian researchers concentrated on many aspects of litterfall including pattern of litterfall;24 nutrient addition by litterfall to soil;25 influences of environmental factors on litterfall;26-27 litterfall nutrient dynamics;28 litter decomposition;29 impact of precipitation on litterfall;30 and, long-term changes in litterfall production.31 Quantitative ecological studies on litterfall largely concentrated on forests of the Himalayas;32 Western Ghats;33 Eastern Ghats;34 and, dry forests35. However, information on litterfall production of Indian dry forests, especially Southern Thorn Forest (STF) has been very limited, thus, the current study was planned to estimate annual litterfall in a legally protected STF ecosystem, namely, Uthumalai Reserve Forest located in Tirunelveli district, Tamil Nadu. The objectives of the current field ecological study were (i) to record litter generation of woody plant community; (ii) to assess the relationships among environmental factors and monthly litter generation; and, (iii) to quantify the litter generation of deciduous and evergreen woody plants.

Materials and Methods

Study area

The current field ecological study was carried out during January to December 2019 in Uthumalai Reserve Forest (URF; 8°59'49.1 "N latitude and 77°35'11.4" E longitude) located in Tirunelveli, Tamil Nadu (Fig. 1). The vegetation of the forest has been classified as southern thorn forest (Sub-group 6A/Type 6A/C1).36 The forest cover of URF is 1300 ha, located 150 to 320 m amsl. The normal annual precipitation is 643.3 mm, in which 64% falls from September to December. Notably, the forest experiences 5-6 dry months in a year, the month December has the low mean temperature (24.5 °C) while the highest was recorded during May (30 °C), (Fig. 2). Red laterite and red loamy are common soil types.37 Acacia planifrons Wright & Arn. (Umbrella thorn), Dalbergia spinosa Roxb. (Prickly Dalbergia), Commiphora berryi (Arn.) Engl. (Indian Balm of Gilead), Grewia flavescens Juss. (Donkey berry), Anogeissus pendula Edgew. (Button tree), and Dichrostachys cinerea (L.) Wright & Arn. (Sickle bush) were found as dominants. Tree density, basal area and species richness was recorded as 4135 trees ha-1, 26 species and 15.238 m2 ha-1, respectively.37 The relationships of climatic variables with components of litter were estimated by Pearson’s simple correlation test (https://datatab.net/statistics-calculator/correlation).

Figure 1: Map of the study area wherein litterfall production of trees recorded

Click here to view Figure

Figure 2: The mean monthly rainfall and temperature recorded in Alagiapandiapuram, located very close to URF for the period from January to December 2019.

Click here to view Figure

Litter sampling and collection

Litterfall of woody plant vegetation was recorded monthly for one calendar year (January to December 2019). A total of 11 litter traps made of fine nylon mesh (pore size 2mm) with 50cm×50cm×100cm (width, length, height) were kept randomly across the forest site.38,39 The fallen litter from each trap was collected and kept in polythene bags, and brought to the laboratory. Litter collected from the forest were separated into leaf, wood (small bark and branch), reproductive parts, and amorphous (inseparable in to organs and degraded). Further, the litter samples kept in forced-air circulating oven at 60 °C for 72 h and dry matter determined. The mean litter generation data obtained from a m2 was extrapolated in to ton ha-1 to facilitate the comparison of the present study with published litterfall studies nationally and globally.

Results

Annual litterfall

The annual litter generation of the study area estimated as 8.058 tons ha-1. The amount of litter falls in a month varied significantly across the litter sampling traps (Fig.3). In addition, the monthly litter fall also differed notably in study area. Litterfall peaked during the month of March (1.2189-ton ha-1; 15.13%) followed by February (1.1925-ton ha-1; 14.80%) and April (1.1523-ton ha-1; 14.01%), whilst the month of September recorded the lowest value (1.582-ton ha-1; 1.96%) (Fig. 4). The percentage contribution of litter classes varied significantly. The leaf constituted the highest proportion of annual litterfall (45.05%, 3.631-ton ha-1) followed by amorphous (27.08%, 2.182-ton ha-1), wood (24.68%, 1.988-ton ha-1), and reproductive organ (3.21%, 0.259-ton ha-1).

The annual litter generation of the study area estimated as 805.81 g m-2 y-1. The amount of fallen litter per month varied significantly across the traps. The litter trap one had a very low amount of litter (11.86±9.87 g per 0.25 m2 area), whereas the trap two had the highest litter (23.67±14.30 per 0.25 m2 area). In addition, the monthly litter fall also differed notably in study area. Litterfall peaked during the month of March (121.89 gm-2; 15.13%) followed by February (119.25 g m-2; 14.80%) and April (115.23 g m-2; 14.01%), whilst the month of September recorded the lowest value (15.82 g m-2; 1.96%) (Fig. 3). The percentage contribution of litter classes varied significantly. The leaf constituted the highest proportion of annual litterfall (45.05%, 363.07 g m-2) followed by amorphous (27.08%, 218.21 g m-2), wood (24.68%, 198.88 g m-2), and reproductive organ (3.21%, 25.92 g m-2).

Figure 3: Amount of monthly litterfall (g m-2) recorded from study area

Click here to View Figure

The amount of four classes of fallen litter differed across the months. The fall of leaf, amorphous, wood and reproductive organs peaked on February (97.05 g m-2), March (32.96 g m-2), March (39.41 gm-2) and September (9.10 g m-2), respectively. Whereas, the lowest amount of litter classes recorded on October (3.33 g m-2), February (2.61 g m-2), October (6.89 g m-2) and July (0.04 g m-2), respectively (Fig. 4).

Figure 4: Contribution of four litter components to total annual litterfall

Click here to view Figure

The amount of four classes of fallen litter differed across the months. The fall of leaf, amorphous, wood and reproductive organs peaked on February (0.971-ton ha-1), March (0.329-ton ha-1), March (0.394-ton ha-1) and September (0.091-ton ha-1), correspondingly. Whereas, the lowest amount of litter classes recorded on October (0.033-ton ha-1), February (0.026-ton ha-1), October (0.069-ton ha-1) and July (0.004-ton ha-1), correspondingly (Fig. 5).

Relationship with monthly litterfall and climate variables

The total litterfall did not show any significant correlation with the mean monthly temperature (p value is 0.128; r2= 0.216) and total monthly rainfall (p = 0.817; r2 = 0.0056). However, mean monthly leaf fall correlated with mean monthly temperature (p = 0.014; p <0.05; r2 = 0.469). The mean monthly wood fall had a relationship with mean minimum monthly temperature (p = 0.032; p <0.05; r2 = 0.382) (Fig. 6). Fig. 6).

Figure 5: Relationship between monthly mean temperature and litterfall.

Click here to view Figure

Figure 6: Relationship between rainfall and litterfall.

Click here to view Figure

Contribution of woody species to leaf litterfall

A sum of 23 woody plant species belonged to 20 genera and 17 families contributed to leaf litterfall. The Mimosaceae and Tiliaceae are the most speciose families (3 species each), followed by Burseraceae and Capparidaceae (2 species each), while 13 families had a single species each. Grewia serrata, Commiphora berryi and Anogeissus pendula constituted 41.71% (1.514-ton ha-1), 18.71% (0.679-ton ha-1) and 8.67% (0.315-ton ha-1) of leaf litter, respectively. These three species constituted 69.1% of annual leaf litterfall (Table 1).

Table 1: Plant name, family, physiognomy and leaf litterfall of trees recorded from study area.

Plant name

Family

Physiognomic group*

Leaf litterfall (ton ha-1 y-1)

1

Grewia serrulata DC.

Tiliaceae

D

1.514

2

Commiphora berryi (Arn.) Engl.

Burseraceae

D

0.679

3

Anogeissus pendula Edgew.

Combretaceae

D

0.315

4

Dalbergia spinosa Roxb.

Papilionaceae

D

0.214

5

Gyrocarpus americanus Jacq.

Hernandiaceae

D

0.187

6

Commiphora caudata (Wright &Arn.) Engl.

Burseraceae

D

0.159

7

Crateva religiosa G.Forst.

Capparidaceae

D

0.151

8

Ziziphus xylopyrus (Retz.) Willd.

Rhamnaceae

EG

0.109

9

Mundulea sericea (Wild.) A.Chev.

Papilionaceae

D

0.088

10

Chloroxylon swietenia DC.

Rutaceae

D

0.045

11

Grewia rotundifolia Juss.

Tiliaceae

D

0.033

12

Ehretia laevis Roxb.

Boraginaceae

EG

0.029

13

Holoptelea integrifolia Planch.

Ulmaceae

D

0.018

14

Acacia planifrons Wright &Arn

Mimosaceae

D

0.015

15

Erythroxylum monogynum Roxb.

Erythroxylaceae

EG

0.015

16

Grewia flavescens Juss.

Tiliaceae

D

0.013

17

Capparis sepiaria L.

Capparidaceae

EG

0.012

18

Carissa spinarum L.

Apocynaceae

EG

0.011

19

Ochna serrulata Walp.

Ochnaceae

D

0.009

20

Albizia amara (Roxb.) B.Boivin

Mimosaceae

D

0.007

21

Reissantia indica (Wiild.) N.Halle

Celastraceae

EG

0.005

22

Dichrostachys cinerea (L.) Wright &Arn.

Mimosaceae

D

0.002

23

Borassus flabelifer L.

Arecaceae

EG

0.001

*D – Deciduous; EG – Evergreen

Physiognomy and leaf litterfall

Of the two physiognomic groups, the deciduous species accounted for 95% (3.449-ton ha-1 y-1) of total annual leaf litterfall, while the evergreen species constituted just 5% (0.181-ton ha-1 y-1). Further, the present study area is dominated by deciduous species both in terms of density and species richness (17 species), while only six are evergreens, represented by a smaller number of individuals. Among families, Tiliaceae contributed the highest amount of annual leaf litterfall 52% (1.560-ton ha-1 y-1), (Table 1).

Of the two physiognomic groups, the deciduous species accounted for 95% (3.449-ton ha-1 y-1) of total annual leaf litterfall, while the evergreen species constituted just 5% (0.181-ton ha-1 y-1). Further, the present study area is dominated by deciduous species both in terms of density and species richness (17 species), while only six are evergreens, represented by a smaller number of individuals. Among families, Tiliaceae contributed the highest amount of annual leaf litterfall 52% (1.560-ton ha-1 y-1), (Table 1).

Amorphous litterfall

Overall, the amorphous class constituted 27.07% (2.182-ton ha-1 y-1) annual total litterfall. The monthly amorphous litter generation ranged from a low of 0.026-ton ha-1 to a high of 0.329-ton ha-1. The amorphous litterfall peaked during the month of March (0.329-ton ha-1; 15.1%) and lowest during the month February (0.026-ton ha-1 y-1;1.2%), (Fig. 4).

Wood litterfall

A total of 1.989-ton ha-1 y-1 (24.68%) wood litterfall recorded from the study area. The range of monthly wood litterfall differed between 0.069 and 0.394-ton ha-1 y-1. The wood litterfall peaked in March (0.394-ton ha-1 y-1; 19.81%), whilst, lowest quantity was recorded in October (0.069-ton ha-1 y-1; 3.47%), (Fig. 4).

Litterfall of reproductive organs

Among four litter classes, reproductive parts (flower, fruit and seed) contributed the lowest amount to the total litterfall. The fall of reproductive organs was highest in September (0.091-ton ha-1 y-1), while, the lowest amount was recorded during the month of July (0.004-ton ha-1 y-1), (Fig. 4).

Discussion

Total annual litter production of the present study area (8.058-ton ha-1 y-1) is comparable to other tropical dry forests, globally and nationally. One of the global reviews on dry forest biome by Murphy and Lugo (1986)40 found annual litterfall of global dry forests as 3.00 to 10.00-ton ha-1 y-1.

The total litter production of southern thorn forest is higher than that of tropical dry forest of southeastern Brazil (4.00 to 4.50-ton ha-1 y-1, 41) tropical forests of Costa Rica (5.30-ton ha-1 y-1,42 6.70 -ton ha-1 y-1, 43), and Acacia albida woodland of Zimbabwe (1.50-ton ha-1 y-1,44). While, the annual litterfall found in STF is lower than in Columbia's dry deciduous forest (8.50-11.00-ton ha-1 y-1)45.

Furthermore, the annual litter generation of the present study area is higher than in Northern dry tropical forest, India (4.88 to 6.71-ton ha-1 y-1,17); dry tropical forests of the Borromeo Wildlife Sanctuary, Chhattisgarh (4.75 to 7.56-ton ha-1 y-1,46); dry tropical forest of Barnowpara Sanctuary, Raipur Forest Division, Chhattisgarh (1.84 to 3.51-ton ha-1 y-1,39); tropical dry thorn forests of Rajasthan (6.00-ton ha-1 y-1,47); dry tropical deciduous forest in Vindhyan highland (4.76-ton ha-1 y-1,48), whereas the annual litterfall of STF is lower than in tropical dry evergreen forest of Villupuram in Tamil Nadu  (13.27 and 13.51-ton ha-1 y-1)3.

Leaf litterfall

In general, among different organs, the leaf constitutes the highest proportion of litterfall in forest ecosystems. In southern thorn forest the leaf litterfall recorded as 45.05%. Earlier, a huge number of studies including King and Campbell (1993)49 from miombo ecosystem (70% leaf litter); Chun-jiang et.al., (2003)5 from European dry forest (70-79%) and European continental forest (64-87%); Pragasan and Parthasarathy (2005)3 from Indian tropical dry evergreen forests (67.9-71.4%); Bisht et al., (2014)8 from Northwest Himalayan subalpine forest (62-78%); Darro and Swamy (2020)50 from Indian tropical dry forest (52.1-91.7%); and, Castellanos-Barliza et al., (2022)51 from Colombian tropical dry forest (>70%) found a higher proportion of leaf litterfall. Environmental factors, rainfall, temperature, elevation, altitude and latitude play major roles in litterfall production. In general, plants in STF tends to have smaller leaves with lesser leaf lifespan.

Relationship among litterfall and climatic variables

The relationship was statistically insignificant between total monthly litterfall and rainfall, and total monthly litterfall and mean monthly temperature. There are reports where no correlation was recorded among annual litterfall, rainfall and temperature in forests around the world. For instance, researchers did not find any relationship between litterfall with climatic factors in montane forest of Costa Rica52; Atlantic forest53; and, open restinga vegetation, Southern Brazil.54 Additionally, in a mangrove forest of Malaysia, Hoque et al., (2015)55 found no relationship among litterfall, rainfall and temperature. Recently, Kassa et al., (2022)56 also did not find any link between litterfall and temperature (r2 = 0.046, p = 0.145), and litterfall and rainfall (r2= 0.010, p = 0.501) from Ethiopia. It has been found that leaves are not shed or flushed only in response to variation in rainfall.57

Conclusions

The annual litterfall production recorded in the present study is higher compared to Indian dry forests located across the states. Litterfall peaked during the month of March (beginning of dry season), it is explicit that the present study area followed a unimodal litterfall pattern. Among four litter classes, the leaves constituted a highest quantity followed by amorphous, wood and reproductive organs. The total monthly litterfall showed no relationship with mean monthly temperature and total monthly rainfall. Further, the deciduous species produced large amount of litter compared to evergreens. Grewia serrata, Commiphora berryi, and Anogeissus pendula together produced a significant amount of litter. This study focused on litterfall production of URF alone, further studies with large number of similar forest sites are needed to understand the actual annual litterfall production of southern thorn forest ecosystem, as the whole.

Acknowledgement

The authors are thankful to the DFO, Tirunelveli for granting the permission to carry out the study.

The authors are thankful to the DFO, Tirunelveli for granting the permission to carry out the study.

Funding source

The authors thank the Science and Engineering Research Board, Ministry of Science and Technology, New Delhi, Government of India for funding this study through a Core Research Grant (CRG/2019/003148).

Conflict of Interest

The authors declare no conflict of interest

Data Availability Statement

The manuscript incorporates all datasets produced or examined throughout this research study.

Ethics Approval Statement

This research did not involve human participants, animal subjects, or any material that requires ethical approval.

Authors’ Contribution

Muthulingam Udayakumar designed and conceptualized the study. Muthulingam Udayakumar and Johnson Evitex-Izayas conducted field surveys, collection and

estimation of litterfall from study area. Johnson Evitex-Izayas prepared the first draft of the manuscript; Muthulingam Udayakumar corrected and revised it.

References

  1. Spain AV. Litter fall and the standing crop of litter in three tropical Australian rain-forests. J Ecol. 1984;72:947-961.
    CrossRef
  2. Ola-Adams BA, Egunjobi JK. Effects of spacing on litterfall and nutrient contents in stands of TectonagrandisLin.f. and Terminalia superba Engl. & Diels. Afr J Ecol. 1992;30(1):18-32.
    CrossRef
  3. Pragasan AL, Parthasarathy N. Litter production in tropical dry evergreen forests of south India in relation to season, plant life-forms and physiognomic groups. Curr Sci. 2005;88:1255-1263.
  4. Krishna MP, Mohan H. Litter decomposition in forest ecosystems: A review. Energy Ecol Environ. 2017;2:236-249.
    CrossRef
  5. Chun-jiang L, Llvesniemi H, Berg B, Kutsch W, Yu-sheng Y, Xiang-qing MA, Westman CJ. Aboveground litterfall in Eurasian forests. J For Res. 2003;14(1):27-34.
    CrossRef
  6. Loubelo E. Comparative study of some elements of the functioning of two eucalyptus stands in Congo, Thesis, University de Rennes. 1990;141.
  7. Bernhard-Reversat F. Dynamics of litter and organic matter at the soil-litter interface in fast-growing tree plantations on sandy ferralitic soils (Congo). Acta Oecol. 1993;14:179-195.
  8. Bisht VK, Nautiyal BP, Kuniyal CP, Prasad P, Sundriyal RC. Litter Production, Decomposition, and Nutrient Release in Subalpine Forest Communities of the Northwest Himalaya. J Ecosyst. 2014; 294867.
    CrossRef
  9. Lozano RR. Leaf litter as a feed resource. In: Lozano RR. Browse Nutrition: Semiarid Regions. USA: Palibrio. 2016;48-52.
  10. Vivanco L, Austin AT. The importance of macro- and micro-nutrients over climate for leaf litter decomposition and nutrient release in Patagonian temperate forests. For Ecol Manag. 2019;441:144-154.
    CrossRef
  11. Udayakumar M, Sekar T. Leaf Traits of Trees in Tropical Dry Evergreen Forests of Peninsular India. Ecologies. 2021;2:268–284.
    CrossRef
  12. Pinos J, Studholme A, Carabajo A, Gracia C. Leaf Litterfall and Decomposition of Polylepis reticulata in the Tree line of the Ecuadorian Andes. Mt Res Dev. 2017;37(1):87-96.
    CrossRef
  13. Kumar BM, Deepu JK. Litter production and decomposition dynamics in moist deciduous forests of the Western Ghats in Peninsular India. For Ecol Manag. 1992;50:181-201.
    CrossRef
  14. Cuevas E. Biology of the belowground system of tropical dry forests. In: Bullock SH, Mooney HA, Medina E. (eds.). Seasonally Dry Tropical Forests. Cambridge: Cambridge University Press.1995;362-383.
    CrossRef
  15. Sanchez-Azofeifa GA, Kalácska M, Quesada M, Calvo-Alvarado JC, Nassar JM, Rodrigues JP. Need for integrated research for a sustainable future in tropical dry forests. Conserv Biol. 2005;19:285–286.
    CrossRef
  16. Chandrasekaran S, Swamy PS. Biomass, litterfall and aboveground net primary productivity of herbaceous communities in varied ecosystems at Kodayar in the western ghats of Tamil Nadu. Agric Ecosyst Environ. 2002;88(1):61-71.
    CrossRef
  17. Singh L. Dry matter and nutrient inputs through litter fall in a dry tropical forest of India. Vegetatio. 1992;98:129-140.
    CrossRef
  18. Matthews E. Global litter production, pools, and turnover times: Estimates from measurement data and regression models. J Geophys Res Atmos. 1997;102(D15):18771-18800.
    CrossRef
  19. Meentemeyer V, Box EO, Thompson R. World patterns and amounts of terrestrial plant litter production. Bioscience. 1982;32:125-128.
    CrossRef
  20. Lonsdale WM. Predicting the amount of litter fall in forests of the world. Ann Bot. 1988;61:319-324.
    CrossRef
  21. Lieth H. Modeling the primary productivity of the world. In: Lieth H, Whitaker RH. (eds.). Primary Productivity of the biosphere. Ney York: Springer-Verlag. 1975:237–263.
    CrossRef
  22. Rodin LE, Basilevic NI. World distribution of plant biomass. In: Functioning of Terrestrial Ecosystems at the Primary Production Level. UNESCO: Proceeding of Copenhagen Symposium. 1968;45-52.
  23. Jha P, Prasad-Mohapatra K. Leaf litterfall, fine root production and turnover in four major tree species of the semi-arid region of India. Plant Soil. 2010;326:481-91.
    CrossRef
  24. Verma Y, Singh L. Pattern of litterfall in tropical dry deciduous forest of central India: A review. RASSA J Sci Soc. 2022; 4(2-3):67-72.

  25. Bhardwaj K. K, Yadav R, Goyal V, Sharma M. K. 2024. Pattern of litterfall production and nutrient addition in soil through litterfall by different tree species: A review. Environ Conserv J. 2024; 25(1):257-266.
    CrossRef
  26. Sharma R, Chaudhry S, Sharma N. K. 2020. Litterfall dynamics in different forest types of Kumaun Himalaya. Res & Rev: J Ecol. 2020; 9(1):23-30.
  27. Ahirwal J, Saha P, Nath A, Nath AJ, Deb S, Sahoo U. K. 2021. Forests litter dynamics and environmental patterns in the Indian Himalayan region. For Ecol Manag. 2021:499:119612.
    CrossRef
  28. Tangjang S, Arunachalam A, Arunachalam K, Deb S. 2015. Litterfall, decomposition and nutrient dynamics in traditional agro-forestry systems of northeast India. Int J Ecol Environ Sci. 2015; 41(1-2):43-53.
  29. Krishna M. P, Mohan M. 2017. Litter decomposition in forest ecosystems: a review. Energy Ecol Environ. 2017; 2:236-249.
    CrossRef
  30. Mehra M. S, Pathak P. C, Singh JS. 1985. Nutrient movement in litter fall and precipitation components for Central Himalayan forests. Ann Bot. 1985; 55(2):153-170.
    CrossRef
  31. Joshi V. C, Sundriyal R. C. Seasonal and long-term changes in litterfall production and litter decomposition in the dominant forest communities of Western Himalaya. Ecol Front. 2024; 44(4):664-672.
    CrossRef
  32. Gairola S. Rawal R. S, Dhar U. Patterns of litterfall and return of nutrients across anthropogenic disturbance gradients in three subalpine forests of west Himalaya, India. J For Res. 2009; 14:73-80.
    CrossRef
  33. Sundarapandian S. M, Swamy P. S. 1999. Litter production and leaf-litter decomposition of selected tree species in tropical forests at Kodayar in the Western Ghats, India. For Ecol Manag. 1999; 123(2-3):231-244.
    CrossRef
  34. Mohanraj R, Saravanan J, Dhanakumar S. 2011. Carbon stock in Kolli forests, Eastern Ghats (India) with emphasis on aboveground biomass, litter, woody debris and soils. iForest-Biogeosci For. 2011;4(2):61-65.
    CrossRef
  35. Rai A, Singh A. K, Ghosal N, Singh N. 2016. Understanding the effectiveness of litter from tropical dry forests for the restoration of degraded lands. Ecol Eng. 2016; 93:76-81.
    CrossRef
  36. Champion H. G. Seth S. K. A. Revised Survey of the Forest Types of India. Delhi: The Manager of Publications, Delhi. 1968.
  37. Evitex-Izayas J, Udayakumar M. Density, diversity and community composition of trees in tropical thorn forest, peninsular India. Curr Bot. 2021; 12:138-145.
    CrossRef
  38. Robertson G. P, Paul E. A. Decomposition and soil organic matter dynamics. In: Sala O. E, Jackson R. B, Mooney H. A, Howarth R. W. (eds). Methods of ecosystem science. New York: Springer, 1999; 104-116.
    CrossRef
  39. Thakur T. K, Thakur A. Litterfall patterns of a dry tropical forest ecosystem of Central India. Ecol Environ Conserv. 2014; 20(3):1-4.
    CrossRef
  40. Murphy P. G, Lugo A. E. Ecology of Tropical Dry Forests. Annu Rev Ecol Evol Syst. 1986; 17(1):67-88.
    CrossRef
  41. Souza e Brito B. G, Fernandes G. W. Litterfall dynamics along a successional gradient in a Brazilian tropical dry forest. For Ecosyst. 2019; 6:1-12.
    CrossRef
  42. Heaney A, Proctor J. Chemical elements in litter in forests on Volcano Barva, Costa Rica. In: Proctor J (ed) Mineral nutrients in tropical forest and savanna ecosystems. Oxford: Blackwell Scientific Publications;1989: 255-271.
  43. Burnham R. J. Stand Characteristics and Leaf Litter Composition of a Dry Forest Hectare in Santa Rosa National Park, Costa Rica. Biotropica. 1997; 29(4):384-395.
    CrossRef
  44. Dunham KM. Litter fall, nutrient-fall and production in an Acacia albida woodland in Zimbabwe. J Trop Ecol. 1989; 5:227-238.
    CrossRef
  45. Jenny H, Gessel S. P, Bingham F. T. Comparative study of decomposition rates of organic matter in temperate and tropical regions. Soil Sci. 1949; 68(6):419-432.
    CrossRef
  46. Jhariya M. K. Influences of Forest Fire on Forest Floor and Litterfall in Bhoramdeo Wildlife Sanctuary (C.G.), India. J For Environ Sci. 2017; 33(4):330-341.
  47. Yadav A. S, Yadav R. K. Litter Fall and Litter Dynamics in a Tropical Dry Deciduous Thorn Forest in Rajasthan in North-West India. Int J Ecol Environ Sci. 2017; 45(5):65-74.
  48. Rai A, Singh A. K, Ghosal N, Singh N. Understanding the effectiveness of litter from tropical dry forests for the restoration of degraded lands. J Ecol Eng. 2016; 93:76-81.
    CrossRef
  49. King J. A, Campbell B. M. Soil organic matter under miombo woodland, plantations and agriculture crops. For Ecol Manag. 1993; 67:225-239.
    CrossRef
  50. Darro H, Swamy S. L. Standing Litter and Litterfall Pattern in Dry Tropical Forests of Achanakmaar-Amarkantak Biosphere Reserve (AABR), India. Int J Curr Microbiol Appl Sci, 2000; 9(4):2000-2007.
    CrossRef
  51. Castellanos-Barliza J, Carmona-Escobar V, Linero-Cueto J, Ropain-Hernández E, León-Peláez J. D. Fine Litter Dynamics in Tropical Dry Forests Located in Two Contrasting Landscapes of the Colombian Caribbean. Forests. 2022; 13(5):660.
    CrossRef
  52. Kohler L, Holscher D, Leuschner C. High litterfall in old-growth and secondary upper montane forest of Costa Rica. Plant Ecol. 2007; 199:163-173.
    CrossRef
  53. Tonin A. M, Goncalves J. F, Bambi P, Couceiro S. R. M, Feitoza L. A. M, Fontana L. E, Hamada N, Hepp L. U, Lezan-Kowalczuk V. G, Leite G. F. M, Lemes-Silva A. L, Lisboa L. K, Loureiro R. C, Martins R. T, Medeiros A. O, Morais P. B, Moretto Y, Oliveria P. C. A, Pereira E. B, Ferreira L. P, Pérez J, Petrucio M. M, Reis D. F, Rezende R. S, Roque N, Santos L. E. P, Siegloch A. E, Tonello G, Boyero L. Plant litter dynamics in the forest-stream interface: precipitation is a major control across tropical biomes. Sci Rep. 2017; 7:10799.
    CrossRef
  54. Gripp A. R, Tavares L. A. F, Brito L. S, Caliman A, Dias A. T. C, Mattos E. A. M, Villela D. M, Silva A. P, Esteves F. A, Martins R. L. Precipitation deficits and high temperature increase leaf litterfall in open Restinga vegetation, in Southern Brazil. Oecol Aust, 2020; 24(4):803-818.
    CrossRef
  55. Hoquea M. M, Kamala A. H. M, Idrisa M. H, Ahmedb O. H, Hoquec A. T. M. R, Billaha M. M. Litterfall production in a tropical mangrove of Sarawak, Malaysia. Zool Ecol. 2015; 25(2):157-165.
    CrossRef
  56. 56. Kassa G, Bekele T, Demissew S, Abebe T. Leaves litterfall and nutrient inputs from four multipurpose tree/shrub species of home garden agroforestry systems. Environ Syst Res. 2022; 11(1):29.
    CrossRef
  57. Chave J, Navarrete D, Almeida S, Alvarez E, Aragao L. E. O. C, Bonal D, Chatelet P, Silva-Espejo J. E, Goret J. Y, von-Hildebrand P, Jimenez E, Patino S, Penuela M. C, Phillips O. L, Stevenson P, Malhi Y. Regional and seasonal patterns of litterfall in tropical South America. Biogeosci. 2010; 7(1):43-55.
    CrossRef
  58. Mohan DS, Arumugam S, Ramaiah S. Diversification and microscopic structure of tissues in endemic and endangered species of Dawkinsia tambraparniei from the river Tamiraparani, Tamil Nadu, India. Environ Sci Pollut Res. 2018; 25:6570-6583.
    CrossRef