The floristic composition of a plant community provides an overall understanding of the structure and functioning of any ecosystem and has frequently been the subject of ecological studies (Singh et al. 2016). In the present study, tree species diversity ranged between 0.42 and 0.85. Generally, monospecific forest types are unable to sustain high floral diversity in contrast to mixed forests which provide heterogenous environment allowing co-existence of various species (Tiwari et al. 2019). Species richness observed in the present study (3–5) are comparable to earlier reported values from temperate forest of Kumaun, Central Himalaya (Bargali et al. 2013; Rana et al. 2015), as well as from temperate forest of Garhwal Himalaya (Singh et al. 2014) and Western Himalaya (Joshi et al. 2021).
In the present study, tree density ranged from 440 to 1050 ha− 1 which is comparable with the values reported for Cypress forests in the previous studies, such as 270–510 ha− 1 by Adhikari et al. (1998) and 460–600 ha− 1 by Rana et al. (2015) from the Central Himalayan forests (Table 7). The variation in tree basal area, ranging from 30.84 to 60.79 m2 ha− 1, suggests diverse age structures across sites, where higher values indicate the dominance of mature trees with lower density, while lower values signify denser stands with a younger demographic composition (Negi et al. 2023).
The values of biomass obtained in the present study are in the range of 223.51–434.6 Mg ha− 1 with highest values recorded from Takula stand whereas, lowest across Dankaniya stand. Differences among stands could be most likely due to vegetation type, species composition, girth class of individual trees, temperature, rainfall pattern and altitude, as these variables have a profound effect on biomass (Pant and Tewari 2020). The biomass values evaluated in the present study are comparable to those reported by Adhikari et al. (1998) for cypress forests in the Nainital region of Central Himalayas, ranging from 239 to 433 Mg ha− 1. When compared with other coniferous species such as Pines, the biomass values of Cypress forests in present study were higher; however, they were lower than those observed for Cedrus deodara and Abies pindrow forests (Table 7). Our study indicates that the density of individual tree species affects total biomass and carbon storage.
The carbon stock trend paralleled that of biomass since carbon content is directly proportional to biomass. Our estimates of carbon stock values (106.2-206.4 Mg C ha− 1) are within the range given by Verma and Garkoti (2019), Lal and Lodhyal (2016), Joshi et al. (2021) for central Himalayan broad leaf forests. While, higher than Pine forests reported by Singh (2019), Gusain et al. (2015), Lal and Lodhyal (2016), Pant and Tiwari (2020), Bisht (2023), and lower than Cedrus and Abies forests (Sharma et al. 2013; Kumar et al. 2024). The reported range of biomass carbon stock at a global scale varies widely across different regions and forest types. For example, in temperate rainforests of USA, it ranges from 506 to 627 Mg C ha− 1 (Smithwick et al., 2002), while in Northeast China temperate and boreal forests, it ranges from 58.9 to 386.5 Mg C ha− 1 (Wei et al., 2013). In Panama, across tropical forests, the range is even broader, from 12.96 to 856.50 Mg C ha− 1 (Ruiz-Jaen and Potvin, 2011). These variations highlight the diverse carbon storage capacities of forests worldwide, influenced by factors such as climate, vegetation type, and land management practices (Singh and Verma 2018).
Table 7
Comparisons of tree density, biomass and carbon stock of present and previous studies in the Central Himalayan forests.
Forests | Region | Location | Altitude (m) | Tree density (ind. ha− 1) | Biomass (Mg ha− 1) | C-stock (Mg C ha− 1) | Reference |
Cypress forest | India | Nainital | 1684-2319.5 | 440–955 | 223.51–434.6 | 106.2-206.4 | Present study |
Oak forest | Almora | 1790–1930 | 390–1500 | 145–503 | 68.29–247.61 | Verma and Garkoti(2019) |
Mixed oak forest | Nainital | 1500–2100 | 910–1100 | 481.05- 568.99 | 228.5- 270.3 | Lal and Lodhyal (2016) |
Oak forest | Nainital | 1750–1950 | 652 | 230.12 | 230.12 | Joshi et al. 2021 |
Mixed-Oak Forest | Nainital | 2000–2250 | 884 | 227.23 | 107.94 |
Pine forest | Nainital | 1600 | 300–300 | 175.5–245.6 | 83.36–116.6 | Singh (2019) |
Pine forest | Almora | 1780–2120 | 1254 | 117.17 ± 10.81 | 55.66 ± 5.13 | Gusain et al. (2015) |
Pine forest | Nainital | 1600 | 1040–1260 | 154–301 | 73–143 | Lal and Lodhyal (2016) |
Pine forest | Nainital | 1750–1850 | 390–3050 | 97.87–158.97 | 46.48–74.66 | Pant and Tiwari (2020) |
Pine forest | Nainital | 1750–1950 | 650 | 285.27 | 135.5 | Bisht 2023 |
Pine forest | Garhwal Himalaya | | 250–300 | 203.02-230.84 | | Shiekh et al. 2012 |
Cypress forest | Nainital | 2100–2325 | 270–510 | 239–433 | – | Adhikari et al. (1998) |
Cypress forest | Nainital | 2120–2325 | 460–600 | 178–431 | 89.07–206 | Rana et al. (2015) |
Himalayan Cupressus torulosa Don. | Jhandidhar, Garhwal | 2100–2500 | 810.0 ± 82.5 | 336.56 ± 62.80 | 154.82 ± 28.89 | Sharma et al. 2013 |
Moist Cedrus deodara Loud. | Binsar, Tarkeshwar, Garhwal | 2200–2500 | 447.5 ± 36.3 | 533.28 ± 39.61 | 245.31 ± 18.22 |
Abies pindrow | Dudhatoli, Garhwal | 2600–3100 | 507.5 ± 21.7 | 377.65 ± 38.64 | 173.72 ± 17.77 |
Siwalik Pinus roxburghii | Fatehpur, Dabrad, Deogaddi, Garhwal | 750–1250 | 685.0 ± 108.0 | 298.04 ± 56.03 | 137.10 ± 25.78 |
Himalayan Pinus roxburghii Sarg | Thalisain, Garhwal | 1500–1800 | 525.0 ± 41.7( | 159.36 ± 15.80 | 73.30 ± 7.27 |
Cedrus deodara pure stand (CDP) | Chail, Solan | 2080 | 303.3 ± 20.8 | 782.6 ± 107.9 | 360 ± 49.7 | Kumar et al. 2024 |
Abies pindrow dominated stand (APD | Churdhar, Sirmaur | 2965 | 546.6 ± 90.7 | 700.2 ± 334 | 322.1 ± 154.1 |
Abies spectabilis pure stand (ASP) | Churdhar, Sirmaur | 3235 | 370 ± 72.1 | 515.5 ± 29.5 | 249.4 ± 18.7 |
Cypress forest | | Northwest Patagonia | 650–1500 | - | 112.2 | 73.2 | Laclau 2002 |
Further, our study showed that biomass and carbon stock peaked at mid altitude followed by high altitude stands. However, our findings didn’t fully support the findings of few previous studies which reported that forest biomass and carbon stocks increase with increasing altitude in the Himalayan region. Most of the forest types studied in this study were mature, fully stocked, old growth forests and had C stocks on the higher end of the values recorded for the forests of the India and elsewhere in the world (Table 7), which infers that these forests have higher amount of C stock. The proportion of above and below ground biomass was observed 83% and 17%, correspondingly, which is consistent to the value reported for Indian forest i.e., 79% and 21% (Chhabra et al. 2002).
The tree carbon sequestration rates ranged between 2.42 to 4.87 Mg ha− 1 yr− 1 across the study sites. Singh et al. (1985) reported a range of carbon sequestration rate of 5–9 Mg ha− 1 yr− 1 in better managed forests and 1.5 to 3 Mg ha− 1 yr− 1 in the medium-quality forests for Uttarakhand forests. When compared with coniferous forests across the world, the carbon sequestration range were within the reported range (Table 8). Stand wise, the Takula stand exhibited highest carbon sequestration rates, likely due to its high tree density and low basal area indicating the predominance of younger trees. Since younger trees grow rapidly, they absorb significant amounts of carbon dioxide from the atmosphere to fuel their growth, leading to higher rates of carbon sequestration (Terakunpisut et al. 2007). It can be concluded that the forest is not yet fully mature, but has the potential to continue sequestering carbon as these trees grow and mature further.
Table 8
Carbon sequestration rate of different forest species in Himalaya and world forests.
Forest | Region | Carbon sequestration rate (Mg ha− 1 yr− 1) | References |
Cypress forest | Kumaun Himalaya, India | 2.42–4.87 | Present study |
P. roxburghii forest | 3.1–6.07 | Pant and Tewari 2013 |
P. roxburghii forest | 0.2–3.96 | Pant and Tewari 2020 |
Oak forests | 2.64 ± 0.27 | Gosain et al. 2015 |
Pine forests | 3.96 ± 0.65 |
Cunninghamia lanceolata | China | 2.15 to 4.20 | Zhang et al. (2007), |
Pinus massoniana | 2.15 to 4.28 |
Pinus banksiana and Picea mariana | Cannada | 2.1–3.7 | Hunt et al. (2010) |
Coniferous forests | Pakistan | 1.65 | Adnan et al. (2015) |
Cunninghamia lanceolata, Cryptomeria japonica, Taiwania cryptomerioides, Chamaecyparis formosensis (plantation forests) | Taiwan | 1.79–4.03 | Yen et al. 2020 |
Temperate forests | | 4.19 | Press et al. 2000 |
Boreal forests | | 1.4 |
In the present study, carbon reserves in soils across cypress stands were higher (9–57%) than those in the trees' biomass (Fig. 3). Soil organic carbon is considered to be one of the largest carbon reservoirs of the terrestrial ecosystems and also plays an important role in the global carbon cycle (Dar and Sundarapandian 2013). The soil organic carbon stocks have been reported to increase with an increase in forest age (Zhu et al. 2010), which was evident across high altitude Naina Peak stands, in our study. The soil carbon stock values in our study were higher than those reported in various studies by Chaturvedi and Melkania (2013), Gosain et al. (2015), Dar and Sundarapandian (2013), Laclau (2000), Zhang et al. (2020), and Zhu et al. (2010), across different coniferous stands worldwide (Table 9). However, they were lower than those reported for boreal forests by IPCC (2007).
Table 9
Soil carbon stock of different forest type in Himalaya and world forests
Forest | Area | SOC (Mg ha− 1) | References |
Cypress forest | Kumaun Himalaya | 173.42–398.80 | Present study |
Mixed Oak Forest | Kumaun Himalaya | 43.81 to 53.47 | Chaturvedi and Melkania 2013 |
Mixed Pine Forest | 110.37 to 125.03 |
Oak forests | 171.8 | Gosain et al. 2015 |
Pine forests | 73.7 |
Pinus wallichiana and Abies pindrow forests | Western Kashmir Himalayas | 50.37 to 55.38 | Dar and Sundarapandian 2013 |
Boreal forest | | 338.8 | IPCC 2007 |
Cypress forest | Andean range, Northwest Patagonia | 109.8 | Laclau 2000 |
Temperate forest | China | 93.7-220.1 | Zhang et al. 2020 |
Temperate mix old growth forest | 62.7–88.7 | Zhu et al. 2010 |
In Himalayas, bioclimatic conditions change rapidly and may vary within short distances resulting in a pronounced heterogeneity of soil types and their chemical and physical properties (Bargali et al. 2018). Our study highlighted highest levels of soil organic carbon (SOC), total nitrogen (TN) and potassium (K) across high altitude C. torulosa stands as indicated by positive correlation between elevation and soil nutrient content. High altitude soils have more soil organic carbon and nitrogen because low temperature causes hyper aridity of soil and suppresses microbial and enzymatic activities which results in slight and slow soil organic matter mineralization and decomposition, thereby affecting the process of nutrient cycling (Charan et al. 2013). The decline in soil nutrient stocks with increasing depth could be attributed to the fact that decomposition of organic matter takes place in the uppermost layers of the soil (Hong, Gan and Chen 2019). In the present study, high C:N ratio at higher altitudes indicate higher availability of N in the forest floor material, whereas, lower ratio in low altitudes stands indicates faster nitrogen release to the soil (Kewlani et al. 2021).
Relationship between carbon storage in both above and below ground component and sequestration rate was negative with available nitrogen and phosphorous levels although observed differences were not significant in most cases. This negative relationship can indicate that nitrogen and phosphorus is being utilized by trees for growth, leading to a depletion in their levels in the soil. Supporting this several studies have shown soils with higher tree biomass tended to have lower available nitrogen and phosphorus levels (Alvarez-Clare et al. 2013; Sun et al. 2013; Hu et al. 2024).