Skip to main content
Scientific Reports logoLink to Scientific Reports
. 2023 Jan 20;13:1117. doi: 10.1038/s41598-023-28276-x

Soil organic carbon, total nitrogen stocks and CO2 emissions in top- and subsoils with contrasting management regimes in semi-arid environments

Chukwuebuka C Okolo 1,2,3,4,5,, Girmay Gebresamuel 1, Amanuel Zenebe 1,2, Mitiku Haile 1, Jephter E Orji 6, Chinyere B Okebalama 7,8, Chinedu E Eze 9,10, Emmanuel Eze 11,12,13, Peter N Eze 5
PMCID: PMC9860075  PMID: 36670181

Abstract

This study aims to investigate soil organic carbon (SOC) and total nitrogen (TN) contents and stocks, CO2 emissions and selected soil properties in croplands, grazing lands, exclosures and forest lands of semi-arid Ethiopia. Sampling was done at 0–30, 30–60 and 60–90 cm soil depths and concentration and stocks of SOC, TN and selected soil properties were determined using standard routine laboratory procedures. There were variations in distribution of SOC and TN stock over 90 cm depth across land use types and locations, decreasing from topsoils to subsoil, with average values ranging from 48.68 Mg C ha−1 and 4.80 Mg N ha−1 in Hugumburda cropland to 303.53 Mg C ha−1 and 24.99 Mg N ha−1 in Desa’a forest respectively. Forest sequestered significant higher SOC and TN stock, decreasing with depth, compared with other land use types. In Desa'a and Hugumburda, the conversion of forest to cropland resulted in a total loss of SOC stock of 9.04 Mg C ha−1 and 2.05 Mg C ha−1, respectively, and an increase in CO2 emission of 33.16 Mg C ha−1 and 7.52 Mg C ha−1 yr−1, respectively. The establishment of 10 years (Geregera) and 6 years (Haikihelet) exclosures on degraded grazing land increased SOC stock by 13% and 37% respectively.

Subject terms: Ecology, Environmental sciences

Introduction

With about 2344 Gt of organic carbon (OC) sequestered in soils across the globe, the soil remains a vital carbon sink1 and is considered the principal terrestrial pool of OC1,2. Soil organic carbon (SOC) is stored both in top and subsoils. It is estimated that the global SOC stock is between 684–724 Pg at 30 cm depth and 1462–1548 Pg at 1 m depth3. At any given depth, SOC stocks depicts a balance between decomposition of organic matter and stabilization of assimilated carbon by soil microorganisms and this balance has the potential to change under different biophysical conditions (land use, vegetation, soil particle size distribution, soil pH, aggregate stability, precipitation)4,5. Furthermore, nitrogen can have control on SOC stocks by changing priming effects connected to N-mediated changes in soil microorganisms6,7. Biophysical gradients are useful to improve our understanding of how environmental and pedogenic factors affect soil processes and properties, because they contain long-term adaptive changes810. Therefore, understanding the distribution of SOC stocks in response to variations in soil physico-chemical properties, soil types and contrasting agro-ecosystems are essential to assess the coupling mechanism between terrestrial carbon–nitrogen cycling, environmental factors and climate change in tropical semi-arid environments.

Human activities tend to increase the size of SOC pool through series of land use including agricultural practices such as afforestation or conversion of cropland into grassland11, cover cropping, alley cropping, no-till and mixed cropping1,1215. Land use change has been widely reported drivers of carbon dynamics in soils1618. The SOC stocks in subsoil horizons originate from plant roots and root exudates, leaching and delivery of dissolved organic matter and bioturbation19. Depending on the nature of the soil, there is also a possibility of transport of clay-bound organic matter and translocation of particulate organic matter into subsoils20. More than 50% of the soil carbon stock is estimated to be found in the subsoil21, characterized by high mean residence time (MRT) and less prone to disturbance compared to topsoils22. Thus, in all terrestrial ecosystems including semi-arid and drylands, subsoils consist a major reservoir of organic C19,21,23. Clays alongside SOC are therefore involved in the formation of stable soil aggregates which minimizes SOC mineralization and depletion24. The importance of the aforementioned sources of SOC in subsoils is dependent on soil processes as well as land use and climatic parameters20. The SOC and nitrogen are interdependent. For example, an increase in CO2 will first lead to an increase in the net primary productivity of the soil ecosystem thereby leading to N immobilization in biomass, depleting soil N, increasing C:N ratio and reducing rates of mineralization25. Soil physicochemical properties including pH, CEC, particle size distribution and BD affect microbial diversity and abundance, and influence carbon and nitrogen cycling processes26,27. In recent times, however, land use and climate change have continued to accelerate the rate of soil aggregate breakdown thereby leading to loss of SOC and N28. Although the common knowledge at the moment is that land use change can result in loss of SOC and N29,30, human activities can lead to increased SOC and N stocks1,11,13, and SOC is generally lesser in semi-arid subsoils6,31, the interaction mechanism among MAP, CEC, clay content, soil pH and bulk density under landuse conversion gradient, and its impacts on depth distribution of SOC, N and CO2 emission in tropical semi-arid soils is still poorly understood16,32.

Ethiopia is a land-locked country with the second largest population in Africa and strategically positioned in the Horn of Africa. A low SOC content (< 1%) is concomitant with dryland soils33, leading to a high occurrence of degradation and an appreciable loss in SOC storage in Ethiopian soils3437. Most studies on SOC stocks and N storage in northern Ethiopia15,38,39 focused only at 0–30 cm depth agricultural plough layer and without consideration of CO2 emissions. Therefore, there is a need for assessment of SOC and N distribution below the ploughing zone given that the impact of land use and climate change on SOC dynamics is not limited to the topsoil alone40.

The objectives of this study are:

  • (i)

    To quantify the distribution of SOC and TN concentrations and stocks and CO2 emissions within the profile to a depth of 90 cm in 30 cm increments in of four contrasting land use types (forest, exclosure, grazing land and cropland);

  • (ii)

    To quantify variations in selected soil properties (total nitrogen, pH, cation exchange capacity (CEC), particle size distribution and bulk density) in these land use types; and.

  • (iii)

    To identify biophysical controls (vegetation, soil properties, climate) on depth distribution of SOC, N storage and CO2 emission in tropical semi-arid soils of northern Ethiopia.

We hypothesized that (i) the impact of vegetation cover/land use on SOC and TN stocks and CO2 emissions in these soils is not limited to the topsoil layer, (ii) climate and land use will serve as possible indicators to modulate the magnitude of changes in SOC and TN stocks, (iii) SOC and TN concentrations and stocks decrease following conversion of forest to grazing land and cropland, but increase with establishment of exclosure on degraded grazing land.

Materials and methods

Description of the study area

Four locations (Fig. 1) with different land use types were chosen for this study: Hugumburda (natural forest, grazing land and cropland, 2494 m.a.s.l), Desa’a (natural forest, grazing land and cropland, 2433 m.a.s.l), Geregera watershed (exclosures, grazing land and cropland, 2180 m.a.s.l) and Haikihelet watershed (exclosures, grazing land and cropland, 2236 m.a.s.l), all in the semi-arid area of Tigray Regional State, northern Ethiopia (Fig. 2; Table 1). Exclosure refers to previously degraded grazing land, which has been fully conserved without any form of animal and human activity as a sustainable way of restoring land degradation through natural regeneration41. The age durations of the exclosures in the Haikihelet and Geregera watersheds are 6 and 10 years respectively42. Cambisols are the dominant soil types in Hugumburda, Haikihelet and Geregera, while Vertisols dominate in Desa’a43.

Figure 1.

Figure 1

Location map of study area showing the study locations in semi-arid area of northern Ethiopia.

Source Authors (ArcMap 10.4).

Figure 2.

Figure 2

Pictorial view of all locations and their land use types (Courtesy of Okolo CC_December 2016).

Table 1.

Site description and meteorological data of study sites. The last crops at the point of sampling are the first two crops in each cropland and all sampled cropland soils were under rainfed cereal cultivation (Adapted from Okolo et al.42,88)

Location (Coordinates) Land use Mean annual temperature (°C) Mean annual precipitation (mm) Geological background Soil type (WRB 2014) Management type/dominant vegetation

Hugumburda

12° 40.441′ N

39° 32.05′

Forest 19 475 Tertiary basalt, alkali-alluvial basalt and tuff Eutric Cambisols Dry Afromontane forest with undergrowth and climbers, mainly Juniperus procera Hochst. ex Endl., Maytenus obscura (A.Rich.) Cufod, Olea europaea ssp. cuspidata (Wall. Ex G.Don), Pterolobium stellatum—Celtis Africana, and Cadia urpurea—Opuntia ficus-indica. Traces of litter removal and tree cutting and carrying (for firewood) by the local dwellers
Grazing land Leptic Cambisols Native grasses with remnants of Acacia and Tehag (shrub savannah) with sparsely grown patches of trees. Lightly and periodically grazed in a communal land. No fertilizer application and no cultivation
Crop land Vertic Cambisols Rainfed cultivation of tef (Eragrostis tef), wheat (Triticum aestivum), Hordeum vulgare (barley), and Maize (Zea mays). NPK/manure application

Haikihelet

13° 39.3853′ N

39° 51.7760′ E

Exclosure 22 498 Limestone Calcaric Cambisols Undisturbed trees and shrubs, mainly Acacia abyssinica Hochst. ex Benth (‘Chea’) and Dodonia. Grazing, cultivation, and any form of human interference/activity is strictly prohibited. No cultivation/fertilization
Grazing land Calcaric Cambisols Native grasses of ‘Rgihe’, ‘Gasa’, ‘Saeri’ and ‘Geza’ with Acacia and Cynodon dactylon (‘Tahay’). Intensively grazed in a communal land. Never cultivated. No fertilizer application
Cropland Calcaric Cambisols Rainfed cultivation of Hordeum vulgare (barley), Triticum aestivum (wheat), and Eragrostis teff (teff). Bunding, ploughing and NPK application/ manure

Desa’a

13° 38.879′ N

39° 46.282′ E

Forest 15 532 Enticho sandstone and Crystalline Precambrian Basement Calcaric Cambisols Dry Afromontane forest, mainly Juniperus procera Hochst. ex Endl., Maytenus obscura (A.Rich.) Cufod, Olea europaea ssp. cuspidata (Wall. Ex G.Don) Cif., Cadia purpurea Ait., and Carissa edulis Vahl., Cadia purpuria (G. Piccioli) Aiton and Tarchonanthus camphoratus L. Traces of litter removal and tree cutting and carrying (for firewood) by the local dwellers
Grazing land Pellic Vertisols Native grasses with remnants of Juniperus and Olei Africana. Lightly and periodically grazed in a communal land. No cultivation and no fertilizer application
Crop land Calcic Vertisols Rainfed cultivation of Hordeum vulgare (barley), Triticum aestivum (wheat) and Eragrostis teff (teff)

Geregera

13° 45.118′ N

39° 43.602′ E

Exclosure 22 507 Adigrat and Enticho sandstones, with inclusion of Paleozoic sedimentary rocks and alluvial sediments Gleyic Cambisols Juniperus procera Hochst. ex Endl. (‘Tsihdi’), Acacia abyssinica Hochst. ex Benth (‘Chea’), Olea European subsp. cuspidata (‘Auli’e’), Dodonea angustifolia L. and Eucalyptus globulus Labill. (‘TsaedaBahrzaf’). Euclea racemose Murr. subsp. schimperi (A.DC.) F. Whit (‘Keleaw’) and Beciumgrandiflorum (‘Tebeb’). No cultivation/fertilization
Grazing land Gleyic Cambisols Different species of ‘Susbania’ and diverse vegetation, including Cynodon dactylon (‘Tahay’) and Hyperrhenia hirta. (‘Goiti ebab’). Lightly and periodically grazed in a communal land. No cultivation/fertilization
Crop land Gleyic Cambisols Rainfed and irrigation** cultivation of cereals: Eragrostis teff (teff), Hordeum vulgare (barley), Triticum aestivum (wheat), Sorghum bicolor (sorghum) and Zea mays (maize); and pulses, example Phaseolus vulgaris (beans), Lens culinaris (lentil) and Pisum sativum subsp. arvense (field pea). Urea/DAP and animal manure application

**Irrigated croplands are among the major land use types in Geregera watershed as practiced by the local smallholder farmers but the irrigated croplands were not sampled in this study.

In the study area, the mean annual precipitation (MAP) between 1983 and 2016 is about 503 mm44. The rainy season peak period is in July/August and rescinds towards September. The estimated average temperature in the region is 18 °C, with significant variations with altitude. The study sites were classified as mid-altitude (1800–2200 m above sea level) and high altitude (> 2100 m above sea level) classes, based on the traditional indigenous agro-climate classification system in Ethiopia.

The most common crop rotation in the study area is wheat + barley + faba bean/field pea, while teff + maize can be switched after a few years. At the time of soil sampling, all cropland was under rainfed cereal crop cultivation. Sampling took place between November and December after harvest, when the soil conditions, particularly bulk density (since bulk density data are used to calculate carbon stocks) of tilled croplands had returned to their original pre-tillage state45,46.

Soil sample collection and preparation

Soil sample collection was done in three soil layers: 0–30, 30–60 and 60–90 cm depth from forest, exclosures, grazing lands and croplands across the four study locations. Deep sampling to a depth of 90 cm with a sampling depth interval of 30 cm was used for the study as previous studies in the area were limited to only 0–30 cm depth. In addition, the deep sampling intervals were assumed to be consistent with the current standard soil depth of 30 cm as proposed for C accounting studies47,48. Systematic sampling was adopted for soil sample collection with transects established in each land use type. Soil samples were collected from three representative plots (50 × 50 m) on the established transect for each land use type. In all land use types, undisturbed samples were first collected using open-faced coring tube, before auger sampling from the same point. A hand-pushed auger was used in collecting the auger samples. Replicate plots within each land use type were approximately 400 m apart and the experimental plots were of the same lithology and management. Within each plot (replicate) in a land use type, auger samples were collected at each depth from four points of a soil profile pit (1.5 × 1 m), along the already established transect, giving four sampling positions per soil depth and twelve samples per land use type. The four soil auger samples collected from each depth were thoroughly mixed together to get one composite (representative) sample per depth in each plot. Nevertheless, in few land use types, sampling depth of 90 cm was not achieved as a result of depth-limiting occurrence of bedrocks at shallow depths. In general, a total number of 104 samples were obtained in all the four locations. Bulk density determination was carried out using the core samples. Bulk density samples were collected with the aid of core samplers, starting from the lowest soil depth (60–90 cm) to the topmost soil depth (0–30 cm). The auger samples were first air-dried, followed by manually removing the visible roots, twigs, debris and leaves, and finally sieving the soil using a 2.0 mm mesh screen. The < 2 mm samples were then subjected to further laboratory analysis.

Laboratory analysis

Soil organic carbon content was determined using modified Walkley and Black wet oxidation method with H2SO4-K2Cr2O7 followed by residual titration with 1 N HCl49. Total nitrogen was determined by the modified macro Kjeldahl digestion method50. Soil pH was measured in soil–water (1:2.5) suspensions51. Cation exchange capacity (CEC) determination was by NH4OAC (pH 7) displacement method52. Bulk density was analyzed using core method53. Particle size distribution was determined by the hydrometer method54 using sodium hexametaphosphate as a dispersant. All measurements were taken in triplicates for improved accuracy.

Calculations, estimations and statistical analyses

The SOC and TN stock in each land use type was calculated with the formula:

SOCorTNMgCha-1=concentration%100×bulkdensityMgm3×areaha×soildepthm 1

where concentration (%) is the percentage concentration of carbon or nitrogen.

The total SOC and TN stocks to the depth of 90 cm across locations in each land type use was calculated by the summation of SOC and TN stocks in the 0–30, 30–60, and 60–90 cm soil depths55.

In Geregera and Haikihelet locations, using the grazing land as a baseline, SOC and TN stocks accumulation in exclosure within the same soil depth were obtained by calculating the difference in SOC and TN between exclosure and grazing land. Due to variation in periods of the different land use types, rate of SOC and TN stocks accumulation for each soil depth of the exclosure land use type was calculated by dividing the estimated accumulation values by the presumed period of exclosure establishment56.

The average age duration of Geregera and Haikihelet exclosures were given as 10 and 6 years respectively42. This simply implies the age duration in years since the exclosures were established from degraded grazing land. This information was based on the oral feedback from farmers (aged 60 years and above) in the study locations.

In Desa’a and Hugumburda locations, SOC and TN losses due to deforestation were estimated by subtracting the total SOC and TN stocks in forestland from its equivalent depth in grazing land or cropland. Thereafter, the calculated loss values were divided by the presumed period of years following land use conversion to get SOC and TN losses per year. The CO2 emission as a result of forest conversion to grazing land and cropland was then established on the basis of the underlying SOC and CO2 relationship as stated by57; which states that 1 Mg ha−1 increase in soil carbon signifies removal of 3.67 Mg of CO2 from the atmosphere. For the purpose of this study, we are focusing only on C lost as CO2 emission without consideration the C losses through erosion, and leaching in the form of dissolved organic C and sediment accumulation. From the obtained results of SOC and TN concentrations and stocks, the distribution trend was explained in the form of high, intermediate and low across the different land use types in all study locations for ease of comparison.

Considering that soil carbon quantity is specifically quantified in a particular soil depth for the purpose of C accounting and budgeting47, effects of land use on SOC and TN concentration and stock, CEC, pH, bulk density, was investigated, comparing them across same depth within site based on two-way analysis of variance (ANOVA). Log transformation of data was carried out before ANOVA whenever assumptions of normality and homogeneity of variances within a group were not obtained. Significant differences (p ≤ 0.05) were determined using Tukey’s honest significant difference (Tukey’s HSD) post hoc test. All the tests were carried using STATISTICA (Version 12.0, StatSoft GmbH, Hamburg, Germany). Factor analysis was performed using version 2014 of XLSTAT (Addinsoft, Paris, France).

Results

Soil organic carbon and total nitrogen (stocks and contents), and C:N ratios in top versus subsoils

Soil organic carbon and total nitrogen stocks and concentrations displayed a similar pattern—decreasing with soil depth among the land use types in all study locations (Fig. 3, Table 2). In Desa’a and Hugumburda, the C stocks per land use type is ranked as, forest (122.98 and 39.26 Mg C ha−1) > grazing land (72.31 and 30.03 Mg C ha−1) > cropland (66.19 and 21.22 Mg C ha−1) in the topsoil layer (0–30 cm depth) respectively (Fig. 3A). The trend of C stock distribution in top soil layer (0–30 cm depth) at Geregera is: exclosure (69 Mg C ha−1) > grazing land (63 Mg C ha−1) > cropland (24 Mg C ha−1), while the distribution trend in Haikihelet showed a similar ranking of: exclosure (105 Mg C ha−1) > grazing land (76 Mg C ha−1) > cropland (69 Mg C ha−1) (Fig. 3A). The TN stock showed significant (p ≤ 0.05) difference between land use types across locations, following a similar distribution pattern with SOC stock (Fig. 3B). Across all locations, SOC and TN stock decreased with soil depth, with high values in forest lands, medium in grazing lands and exclosures, and low in crop lands. The SOC and TN content (%) followed similar trend as the SOC and TN stock distribution (Table 2), decreasing with soil depth in all land use types across locations.

Figure 3.

Figure 3

Soil organic carbon stock (A) and soil nitrogen stock (B) as influenced by land use and soil depth at Geregera, Haikihelet, Desa’a, and Hugumburda. Error bars represent the standard error of means. Letters above the error bars indicate significant differences (p ≤ 0.05) between land uses at 0–30 cm (a), 30–60 cm (a′) and 60–90 cm (a″).

Table 2.

Soil organic carbon and total nitrogen concentrations, C:N ratio, cation exchange capacity and pH under different land use types and soil depths in the study locations.

Location Land use Depth (cm) Soil organic carbon (%) Total nitrogen (%) C:N CEC (C mol kg−1) pH (H2O)
Hugumburda Forest 0–30 1.16 ± 0.11c 0.07 ± 0.00a 15.66 ± 0.05a 58.12 ± 0.12c 7.90 ± 0.06b
30–60 0.66 + 0.17c′ 0.08 ± 0.03a′ 8.79 ± 0.10a′ 56.52 ± 0.14b′ 7.75 ± 0.02b′
60–90 0.53 ± 0.03b″ 0.03 ± 0.01a″ 20.00 ± 0.02b″ 50.95 ± 0.17a″ 7.85 ± 0.03c″
Grazing land 0–30 0.85 ± 0.20ab 0.08 ± 0.01a 11.31 ± 0.11a 34.39 ± 0.00a 7.55 ± 0.03a
30–60 0.40 + 0.00ab′ 0.03 ± 0.00a′ 12.21 ± 0.00a′ 28.12 ± 3.18a′ 7.60 ± 0.00a′
60–90 0.40 ± 0.01a″ 0.04 ± 0.00a″ 10.10 ± 0.00a″ 19.02 ± 0.00b″ 7.60 ± 0.00a″
Crop land 0–30 0.50 ± 0.06a 0.05 ± 0.01a 11.21 ± 0.04a 45.27 ± 2.55b 8.05 ± 0.02c
30–60 0.25 + 0.03a′ 0.03 ± 0.00a′ 7.66 ± 0.02a′ 32.65 ± 2.87a′ 7.90 ± 0.00c′
60–90 0.40 ± 0.00a″ 0.04 ± 0.01a″ 9.86 ± 0.01a″ 39.12 ± 6.29a″ 7.75 ± 0.03b″
Haikihelet Exclosure 0–30 2.83 ± 0.50a 0.20 ± 0.09a 14.15 ± 0.29a 30.51 ± 2.24b 7.90 ± 0.00a
30–60 1.74 + 0.07a′ 0.14 ± 0.00b′ 12.42 ± 0.04b′ 19.55 ± 3.78a′ 7.96 ± 0.03a′
60–90 1.46 ± 0.01c″ 0.11 ± 0.06a′′ 13.27 ± 0.01a″ 14.63 ± 0.00a″ 8.00 ± 0.00a″
Grazing land 0–30 2.09 ± 0.13a 0.14 ± 0.01a 15.13 ± 0.07a 15.12 ± 6.05a 7.30 ± 0.00b
30–60 1.54 + 0.14a′ 0.08 ± 0.01a′ 18.55 ± 0.07a′ 5.25 ± 0.85b′ 7.55 ± 0.03b′
60–90 0.59 ± 0.0a″ 0.03 ± 0.00a′′ 18.90 ± 0.00b″ 3.60 ± 1.36b″ 7.80 ± 0.00a″
Crop land 0–30 1.83 ± 0.03a 0.26 ± 0.08a 7.04 ± 0.06b 24.95 ± 0.05ab 7.95 ± 0.03a
30–60 1.54 + 0.03a′ 0.08 ± 0.00a′ 19.25 ± 0.01b′ 17.28 ± 3.75a′ 7.95 ± 0.02a′
60–90 1.00 ± 0.00b″ 0.07 ± 0.01a″ 14.28 ± 0.03a″ 17.12 ± 0.00a″ 8.10 ± 0.00a″
Desa′a Forest 0–30 3.88 ± 0.00c 0.36 ± 0.01b 10.88 ± 0.01a 25.83 ± 2.99a 7.40 ± 0.06b
30–60 3.04 + 2.00c′ 0.25 ± 0.09b′ 12.27 ± 0.15a′ 23.40 ± 1.98a′ 7.65 ± 0.03b′
60–90 2.44 ± 0.04b″ 0.17 ± 0.03c″ 14.36 ± 0.04a″ 19.63 ± 3.12a″ 7.75 ± 0.03c″
Grazing land 0–30 2.09 ± 0.04b 0.16 ± 0.00a 13.01 ± 0.02a 32.28 ± 0.99a 7.25 ± 0.03a
30–60 1.55 + 0.01b′ 0.11 ± 0.01a′ 13.73 ± 0.01a′ 28.27 ± 0.00a′ 7.20 ± 0.00a′
60–90 1.47 ± 0.00a″ 0.08 ± 0.00b″ 17.91 ± 0.00a″ 24.47 ± 1.98a″ 7.30 ± 0.00a″
Crop land 0–30 1.80 ± 0.02a 0.11 ± 0.01a 16.63 ± 0.01a 28.97 ± 0.43a 7.55 ± 0.02c
30–60 0.89 + 0.19a′ 0.06 ± 0.00a′ 14.83 ± 0.10a′ 26.63 ± 2.58a′ 7.75 ± 0.02c′
60–90 1.14 ± 0.20a″ 0.05 ± 0.01a″ 22.80 ± 0.10a″ 21.81 ± 2.02a″ 7.45 ± 0.03b″
Geregera Exclosure 0–30 1.48 ± 0.57ab 0.08 ± 0.02a 18.86 ± 0.29b 18.52 ± 3.06a 7.55 ± 0.03a
30–60 0.92 + 0.21a′ 0.07 ± 0.01a′ 12.84 ± 0.11b′ 19.84 ± 1.58a′ 7.50 ± 0.00a′
60–90 0.62 ± 0.18a″ 0.07 ± 0.00a″ 9.11 ± 0.09a″ 8.35 ± 4.09a″ 7.50 ± 0.00a″
Grazing land 0–30 1.88 ± 0.10b 0.13 ± 0.01a 14.89 ± 0.05ab 24.59 ± 6.57a 7.50 ± 0.00a
30–60 1.19 + 0.22a′ 0.07 ± 0.01a′ 18.09 ± 0.11c′ 24.52 ± 8.84a′ 7.45 ± 0.03a′
60–90 0.71 ± 0.19a″ 0.05 ± 0.01a″ 15.87 ± 0.10b″ 19.68 ± 8.99a″ 7.35 ± 0.03b″
Crop land 0–30 0.58 ± 0.08a 0.08 ± 0.01a 7.25 ± 0.05a 14.64 ± 0.66a 8.10 ± 0.00b
30–60 0.57 + 0.08a′ 0.08 ± 0.01a′ 7.13 ± 0.04a′ 10.94 ± 0.03a′ 7.80 ± 0.06b′
60–90 0.61 ± 0.05a″ 0.06 ± 0.01a″ 10.16 ± 0.03a″ 6.44 ± 1.53a″ 7.55 ± 0.03a″

 ± Mean followed by standard errors. Letters after the standard errors indicate significant differences (P < 0.05) between land uses at 0–30 cm (a), 30–60 cm (a′) and 60–90 cm (a″).

There was no clear distribution pattern of C:N ratio with depth under different land use types. The soil C:N ratios were high in forest and low in cropland across locations, except for the cropland in Desa’a which recorded higher C:N ratio than forest (Table 2). Across all locations, the soil C:N ratios ranged between 22.80 and 7.04.

Accumulation and loss of SOC and TN stock

With exclosure establishment, high SOC stock accumulation in Geregera (16.57 Mg C ha−1) and Haikihelet (64.20 Mg C ha−1) was observed (Table 3). The high SOC accumulation also accounted for a high SOC accumulation rate of 6.88 Mg C ha−1 yr−1 in Geregera and 10.7 Mg C ha−1 in Haikihelet. The TN accumulation and rate of TN accumulation for Geregera and Haikihelet were 0.18 Mg N ha−1 and 0.02 Mg TN ha−1 yr−1 and 1.29 Mg N ha−1 and 0.22 Mg TN ha−1 yr−1 respectively (Table 3). The estimated total loss of SOC resulting from forest conversion to cropland led to SOC loss of 9.04 Mg ha−1 yr−1 and 2.05 Mg ha−1 yr−1 in Desa’a and Hugumburda respectively. Also, conversion of forest to grazing land accounted for a total SOC loss of 3.50 Mg ha−1 yr−1 and 0.61 Mg ha−1 yr−1 in Desa’a and Hugumburda, respectively (Table 4). Similarly, forest conversion to cropland gave rise to emission of 33.16 Mg ha−1 yr−1 CO2 and 7.52 Mg ha−1 yr−1 CO2 in Desa’a and Hugumburda, respectively (Table 4). More so, the conversion of forest to grazing land accounted for an emission of 12.84 Mg ha−1 yr−1 CO2 and 2.21 Mg ha−1 yr−1 CO2 in Desa’a and Hugumburda respectively.

Table 3.

Magnitude and rate of soil organic carbon (SOC) and total nitrogen (TN) stocks accumulation in exclosures at 0–90 cm depth in Geregera and Haikihelet [grazing land as baseline].

Location Land use Assumed duration since conversion (Year) SOC stock (Mg C ha−1) SOC Accumulation (Stock—Cropland) (Mg C ha−1) Rate of SOC Accumulation (Mg C ha−1 yr−1) TN stock (Mg N ha−1) TN Accumulation (Stock—Cropland) (Mg N ha−1) Rate of TN Accumulation (Mg N ha−1 yr−1)
Geregera Grazing exclosure 128.28 9.17
10 144.85 16.57 1.66 9.35 0.18 0.02
Haikihelet Grazing exclosure 171.48 15.86
6 235.68 64.2 10.7 17.15 1.29 0.22

Table 4.

Soil carbon and nitrogen loss and calculated potential carbon dioxide emission related to a change in land use (conversion from forest [baseline] to grazing and cropland) in Desa’a and Hugumburda.

Location Land use Depth (cm) SOC loss (Mg C ha−1 yr−1) N loss (Mg N ha−1 yr−1) CO2 loss (Mg C ha−1 yr−1)
Desa’a Grazing land 0–30 1.52 0.17 5.58
30–60 1.33 0.12 4.88
60–90 0.65 0.07 2.38
Total 3.50 0.36 12.84
Crop land 0–30 3.41 0.44 12.50
30–60 3.52 0.32 12.92
60–90 2.11 0.23 7.74
Total 9.04 0.99 33.16
Hugumburda Grazing land 0–30 0.28 0.00 1.02
30–60 0.16 0.03 0.58
60–90 0.17 0.00 0.61
Total 0.61 0.03 2.21
Crop land 0–30 1.08 0.05 3.97
30–60 0.73 0.07 2.69
60–90 0.24 0.00 0.86
Total 2.05 0.12 7.52

Regarding TN loss, forest conversion to cropland accounted for a TN loss of 0.99 Mg ha−1 yr−1 and 0.12 Mg ha−1 yr−1 in Desa’a and Hugumburda respectively. More so, conversion of forest to grazing land accounted for very low TN loss in Desa’a and Hugumburda (Table 4).

In Desa’a and Hugumburda, conversion of forest to grazing land and cropland accounted for huge SOC stock depletion amounting to 30 to 50% of the SOC in the topsoil layer. Forest conversion to grazing land in Desa’a resulted to a reduction in total SOC and TN stock of 3.50 Mg C ha−1 yr−1 and 0.36 Mg N ha−1 yr−1 in grazing land, and 9.04 Mg C ha−1 yr−1 and 0.99 Mg N ha−1 yr−1 in cropland respectively. Hugumburda followed the same pattern of SOC and TN stock loss, though with less magnitude accounting for estimated total SOC and TN stock loss of 0.61 Mg C ha−1 yr−1 and 0.03 Mg N ha−1 yr−1 in grazing land, and 2.05 Mg C ha−1 yr−1 and 0.12 Mg N ha−1 yr−1 in cropland respectively (Table 4).

Soil physicochemical properties

The CEC was consistently higher in the upper (0–30 cm) than the lower (30–60 and 60–90 cm) soil layers under all land use types across locations. The highest CEC value of 58.12 cmol kg−1 was recorded in the 0–30 cm forest soil at Hugumburda with the least CEC value obtained at 60–90 cm grazing land at Haikihelet (3.60 cmol kg−1) (Table 2).

In Vertisols of Desa’a location, no land use effect on CEC was observed, whereas in all other locations, predominated by Cambisols, croplands displayed higher CEC values more than grazing land, with the exception of Geregera. There was an observed decrease in CEC content across soil depths in all land use types in studied locations.

Land use types and soil depth affected the pH value of the soils, though with narrow margin across locations. The highest soil pH of 8.10 was recorded in Geregera cropland 0–30 and Haikihelet cropland 60–90 while the least soil pH value of 7.2 was recorded in subsoil (30–60 cm) of Desa’a grazing land (Table 2). Generally, the soil pH was in the slightly alkaline range in the study area (Table 2).

Particle size distribution of the soils showed significant (p ≤ 0.05) variations across depths under different land use types (Table 5) with an exception in Hugumburda where total sand and silt fractions showed no significant difference (p ≥ 0.05) across depths among land use types. Predominance of total sand fraction in Cambisols of Hugumburda and Geregera in different land use types was observed. In Cambisols of Haikihelet, total sand fraction was dominant in exclosure, while clay and silt fractions were dominant in grazing land and cropland respectively. In Vertisols of Desa’a, silt fraction was dominant in forestland while clay fraction was dominant in grazing land and cropland. Clay fraction increased with depth in most land use types across locations except in Hugumburda (forest and grazing land), Haikihelet (forest, grazing land and cropland) and Desa’a (forest) (Table 5).

Table 5.

Soil physical properties under different land uses and soil depths in the study locations.

Location Land use Depth (cm) Total sand (%) Silt (%) Clay (%) Textural class (USDA) Bulk density (Mg/m3)
Hugumburda Forest 0–30 46.00 ± 0.57a 43.00 ± 2.30a 11.00 ± 1.73a Loam 1.13 ± 0.01a
30–60 48.00 + 4.03a′ 40.00 ± 4.00a′ 12.00 ± 0.00a′ Loam 1.15 ± 0.01b′
60–90 59.00 ± 1.15a″ 30.00 ± 0.58a″ 11.00 ± 0.58a″ Loam 1.31 ± 0.07a″
Grazing land 0–30 44.00 ± 5.20a 39.00 ± 5.77a 17.00 ± 0.57a Loam 1.19 ± 0.04a
30–60 57.00 + 0.00a′ 27.00 ± 0.00a′ 16.00 ± 0.00a′ Sandy Loam 1.45 ± 0.00a′
60–90 49.00 ± 0.00a″ 39.00 ± 0.00a″ 12.00 ± 0.00a″ Sandy Loam 1.26 ± 0.00a″
Crop land 0–30 46.00 ± 1.73a 42.00 ± 4.04a 12.00 ± 2.31a Loam 1.38 ± 0.08b
30–60 49.00 + 5.77a′ 37.00 ± 8.08a′ 14.00 ± 2.20a′ Loam 1.44 ± 0.07a′
60–90 48.00 ± 5.19a″ 35.00 ± 6.93a″ 17.00 ± 1.73b″ Loam 1.42 ± 0.18a″
Haikihelet Exclosure 0–30 45.00 ± 4.62b 32.00 ± 0.58a 23.00 ± 5.19a Loam 1.21 ± 0.01a
30–60 39.00 + 6.93b′ 35.00 ± 1.15a′ 26.00 ± 8.08a′ Clay Loam 1.28 ± 0.06a′
60–90 57.00 ± 0.00b″ 33.00 ± 0.00a″ 10.00 ± 0.00b″ Sandy Loam 1.53 ± 0.00b″
Grazing land 0–30 18.00 ± 5.19a 30.00 ± 0.58a 52.00 ± 5.77b Clay 1.25 ± 0.05a
30–60 13.00 + 4.62a′ 30.00 ± 4.04a′ 57.00 ± 8.66b′ Clay 1.37 ± 0.14a′
60–90 20.00 ± 7.51a″ 27.00 ± 4.62a″ 53.00 ± 12.12b″ Clay 1.36 ± .10ab″
Crop land 0–30 23.00 ± 3.46a 45.00 ± 2.31b 32.00 ± 5.77a Clay Loam 1.26 ± 0.08a
30–60 14.00 + 0.58a′ 57.00 ± 4.62b′ 29.00 ± 4.04a′ Silty clay loam 1.39 ± 0.05a′
60–90 19.00 ± 0.00a″ 49.00 ± 0.00b″ 32.00 ± 0.00ab″ Silty clay loam 1.29 ± 0.00a″
Desa’a Forest 0–30 30.00 ± 6.35a 40.00 ± 5.19b 30.00 ± 1.15a Clay loam 1.06 ± 0.00a
30–60 28.00 + 6.35b′ 43.00 ± 9.24b′ 29.00 ± 2.89b′ Clay loam 1.06 ± 0.00a′
60–90 22.00 ± 5.19b″ 47.00 ± 5.77b″ 31.00 ± 0.58b″ Silty clay loam 1.14 ± 0.01b″
Grazing land 0–30 30.00 ± 6.35a 32.00 ± 2.89ab 38.00 ± 9.24a Clay loam 1.15 ± 0.06ab
30–60 12.00 + 1.73a′ 26.00 ± 2.89ab′ 62.00 ± 4.62a′ Clay 1.13 ± 0.05a′
60–90 9.00 ± 0.00ab″ 19.00 ± 0.00a″ 72.00 ± 0.00a″ Clay 1.41 ± 0.00a″
Crop land 0–30 9.00 ± 00.00b 23.00 ± 0.00a 68.00 ± 0.00b Clay 1.22 ± 0.01b
30–60 8.00 + 0.58a′ 20.00 ± 1.73a′ 72.00 ± 2.31a′ Clay 1.44 ± 0.05b′
60–90 7.00 ± 1.15a″ 23.00 ± 2.31a″ 70.00 ± 3.46a″ Clay 1.42 ± 0.03a″
Geregera Exclosure 0–30 49.00 ± 1.15a 28.00 ± 0.58a 23.00 ± 1.73a Sandy clay loam 1.23 ± 0.06a
30–60 48.00 + 5.19a′ 25.00 ± 8.08a′ 27.00 ± 2.89a′ Sandy clay loam 1.26 ± 0.01a′
60–90 56.00 ± 6.35a″ 19.00 ± 6.93a″ 25.00 ± 0.58a″ Sandy clay loam 1.41 ± 0.01a″
Grazing land 0–30 40.00 ± 4.04b 26.00 ± 0.58a 34.00 ± 3.46b Clay loam 1.49 ± 0.10b
30–60 47.00 + 16.17a′ 13.00 ± 3.46a′ 40.00 ± 12.70a′ Sandy clay 1.38 ± 0.01a′
60–90 49.00 ± 17.32a″ 12.00 ± 4.04a″ 39.00 ± 12.28a″ Sandy clay 1.43 ± 0.03a″
Crop land 0–30 51.00 ± 1.15a 22.00 ± 0.58b 27.00 ± 0.58ab Sandy clay loam 1.44 ± 0.04ab
30–60 45.00 + 6.93a′ 19.00 ± 3.46a′ 36.00 ± 3.46a′ Sandy clay loam 1.39 ± 0.05a′
60–90 39.00 ± 6.92a″ 19.00 ± 4.62a″ 42.00 ± 2.31a″ Clay 1.51 ± 0.04a″

 ± Mean followed by standard errors. Letters after the standard errors indicate significant differences (p < 0.05) between land uses at 0–30 cm (a), 30–60 cm (a′) and 60–90 cm (a″).

Bulk density (BD) differed significantly (p ≤ 0.05) with depths across different land use types in the studied locations. Similarity existed between topsoil BD of grazing land and cropland. Across locations, the highest BD value of 1.53 Mg/m3 was recorded in 60–90 cm of Haikihelet exclosure while the lowest BD value of 1.06 Mg/m3 was recorded in both 0–30 and 30–60 cm depth in Desa’a forestland. Significant increase in BD with depth was observed across locations (Table 5).

Factor analysis across locations

In Geregera, the first factor axis (F1) of the biplots relates to plots gradient from grazing land to cropland, however, there is similarity between the plots of grazing land and forest land. Most of the studied soil properties (SOC, TN, C:N ratio, CEC, SOC and TN stock, pH, % silt and % clay) were higher in exclosure and grazing land compared to cropland (Fig. 4A). Notably, cropland soils are characterized by loam, sandy loam, silty clay loam and sandy clay loam texture for Hugumburda, Haikihelet, Desa’a and Geregera respectively (Table 2), in addition to low SOC content as observed in the second factor axis (F2) which explained 23.80% of the total variance. In general, this relates to a particular gradient of low SOC (cropland plots) to high SOC (exclosure plots) (Fig. 4A).

Figure 4.

Figure 4

Biplots of (A) Geregera (B) Desa’a, and (C) Haikihelet locations as influenced by land use. Soil physico-chemical characteristics: BD = bulk density, Soil texture (sand%, silt% and clay%), SOC = soil organic carbon, TN = total nitrogen, CEC = cation exchange capacity, CN = C:N ratio. The red arrow denotes the direction of the high weighting of soil physico-chemical characteristics in the first (FA-1) and second factor (FA-2).

In Desa’a, the first factor axis (F1) of the biplots followed particular pattern modulated by percent clay distribution. Cropland has higher percent clay content, followed by grazing land, with forest land recording the least percent clay content (Fig. 4B). The second factor axis (F2) of the biplots indicates a pattern of inclination from forest to cropland plots. However, a clear pattern was observed, starting from forest with high SOC and high sand fraction to cropland with low SOC and low sand fraction (Fig. 4B).

The biplots in Haikihelet indicated that the first factor axis (F1) exhibited a clear pattern of inclination from exclosure to cropland plots. The second factor axis (F2) followed a different pattern of increment from cropland to grazing land, corresponding to a gradient of low to high SOC pool. The grazing land is characterized by high SOC content, SOC stock and high clay content. (Fig. 4C).

It was observed that the biplots in Hugumburda both for the first factor axis (F1) and second factor axis (F2) of the biplots explained approximately 65% of the variances in the components (Fig. 5A), thus necessecitating to incorporate third factor axis (F3) (Fig. 5B). The first factor axis (F1) explained 41.25% of the total variance in forest and partly in grazing land, consisiting of variables indicative of soil nutrient availability (SOC, TN, SOC stock, TN stock, CEC, and C:N ratio) (Fig. 5A). The second factor axis (F2) which explained 23.62% of the total variance, was characterized by % clay, BD and pH in cropland and grazing land. The third factor axis (F3) explained 19.70% of total variation, and was characterized by pH and BD in grazing land and cropland and so, reflects the impact of anthropogenic activities (Fig. 5B).

Figure 5.

Figure 5

Biplots of Hugumburda depending on landuse indicating (A) Factor axis F1 and F2, and (B) Factor axis F1 and F3, as influenced by land use. Soil physico-chemical characteristics: BD = bulk density, Soil texture (sand%, silt% and clay%), SOC = soil organic carbon, TN = total nitrogen, CEC = cation exchange capacity, CN = C:N ratio. The red arrow denotes the direction of the high weighting of soil physico-chemical characteristics in the first (FA-1) and second factor (FA-2).

Discussion

Significant difference in SOC and TN stocks was observed among various land use types across depths, with clear differences in distribution trend across locations. The high SOC and TN concentration recorded in topsoil (0–30 cm) of forest and exclosure could be as a result of minimal disturbance in these ecosystems, litter accumulation from trees and shrubs, below ground litter and high biomass cover5860. In addition, SOC and TN distribution at lower depth in most land use types were usually low at 60–90 cm depth, thus indicating that effect of land-use was mainly limited to the upper soil layers. This did not support our first hypothesis which states that the impact of land use is not limited to the topsoil. The significantly lower concentrations of SOC and TN especially in cropland soils across depths could be attributed to unsustainable farm practices like total harvesting without residue retention thus exposing the soil to incidences of soil and water erosion, residue burning and intensive tillage operations which exacerbates decomposition and high rate of SOM oxidation due to continuous cultivation6163. However, with good management practices in croplands, C retention and stabilization can be enhanced.

A possible attribution of high SOC contents at Haikihelet and Desa’a is the high clay content recorded in these locations (See Table 5). In this study, both SOC and clay contents were found to be higher in Vertisols (clay dominated) than Cambisols (sandy loam dominated). This finding is in line with works of64 and65 who reported that clay textured soils had higher SOC content in studies assessing distribution of SOC levels and structural indices under contrasting land use types in southeastern Nigeria.

The forest sequestered more SOC stock than other studied land use systems, with high sequestration in topsoils. This is in line with the report of16 that forest soils are great C pools of terrestrial ecosystems in the global C cycle. This implies a high risk of CO2 release from these forest topsoils if they are eventually deforested or converted to cropland. The low SOC stocks in the cropland are attributable to the total harvest, tillage activities in addition to leaching and erosion losses and reduced organic material going back to the soil, soil and water erosion leading to loss of SOM, regular tillage and cropping activities accounting for high oxidation rates of SOM, burning of crop residues19,61,66.

Our results show that C:N ratio was affected by land use types, but there was no definite distribution trend. This suggests that the sole use of C:N ratio as a SOM quality indicator is limited and quite misleading67. The lowest C:N ratio in 30–60 cm depth in cropland soil of Hugumburda (7.66) corresponds to a very low SOC content of 0.25% (Table 2). The ratio was much narrower in croplands (with the exception of Desa’a cropland) than other land use types, which is an indication of high mineralization and oxidation rate in cropland soils. Decline in C:N ratio with soil depth is evident in most agricultural soils68. Interpretation of changes in C:N ratio due to in land use changes or management practices is complex and has been suggested to be better treated separately from SOC and TN concentrations and stocks, and on a case by case basis for clear understanding67.

At Geregera and Haikihelet, taking grazing land as the baseline, increase in SOC and TN stock accumulation as a result of exclosure establishment was recorded. The observed improvement in SOC and TN stock in 6- and 10-year-old exclosure in Haikihelet and Geregera respectively is attributed to increase in organic inputs due to vegetation restoration and restriction of animal grazing on exclosures. This firmly supports section of our third hypothesis which states that exclosure establishment on degraded ecosystems results in SOC restoration. The implication of our result is that long age duration of exclosures may not necessarily result to remarkable replenishment of soil nutrients on previously degraded grazing land in compared to short-term exclosures. Site-specific characteristics and micro-climatic conditions across locations might have contributed to these variations in SOC accumulation rates.

Most of the SOC and TN stocks losses were in the 0–30 cm topsoil layer across land use types (Table 4). Similar trend in SOC loss has been previously reported by34 who indicated that forest conversion to crop land, open grazing, and plantation accounted for an estimated decline in SOC stock in the topsoil layer amounting to 0–63% in cropland, 0–23% in open grazing land, and 17–83% in plantation. This confirms a section of our third hypothesis which states that SOC concentrations and stocks decrease after conversion of natural forests to cultivated lands. In the dry Afromontane remnant pristine forests in northwest Ethiopia, huge reduction in SOC stock of up to 87% and 50% with the conversion of forest to cropland at Katassi and Gelawdios sites respectively was reported by59. This portends a huge threat to global warming in the face of climate change.

Overall, with forest conversion to cropland and grazing land, the estimated CO2 emission as obtained in this study is huge and capable of contributing to atmospheric greenhouse gas effect. The CO2 emissions decreased with soil depth with higher emissions in cropland compared to grazing land soils. Notably, CO2 fluxes decreases appreciably with depth though not significantly contributing to surface fluxes69,70. This implies that any form of subsoil disturbance could affect the deep subsoil CO2 reservoir. Thus, mobility of CO2 in the subsoil to the surface soil is impaired and may be entrapped in soil pores and solution if undisturbed, or used by subsoil autotrophs19. In cropland soils with high CO2 emissions, these CO2 loss effects can be compensated by the accrual of deep root C inputs from deep-rooting crops. Recent studies of deep-rooted perennial grasses planted in C-poor soils reported no effect of these crops on surface CO2 fluxes in different soil types71,72. Nevertheless, the value of SOC loss in our study indicates that loss of SOC may not only be as a result of CO2 emission to the atmosphere73 but can as well be lost due to leaching in the form of dissolved organic carbon, erosion and sediment accumulation, which were not considered in this study. Thus, the actual fate of this SOC loss across landscape in semi-arid area of northern Ethiopia is still not well-known and there is need for further detailed investigation.

Rainfall has been reported as the main governing factor of SOM and TN content distribution in Sub-Saharan tropical soils of East Africa74. This was affirmed by our result of overall mean high SOC and TN stock especially in Desa’a with high rainfall and low temperature compared to other locations (See Figs. 6 and 7). Observably, SOC stock increased with increasing mean annual precipitation (MAP) and decreased appreciably with increasing mean annual temperature (MAT) (See Figs. 6 and 7). Various authors have reported positive correlation of SOC stock with MAP but with negative correlation with MAT59,75. Assefa et al.59 reported high SOC stock values in areas with high MAP compared to areas with low MAP in northwest Ethiopia. Estimated SOM content ranging between 0.5–3.0 and 10–13% for tropical soils of Sub-Saharan Africa (high temperature) and temperate soils of Europe/America (low temperature) respectively has been reported2. Global distribution of SOC stock follows a pattern, increasing from temperate (cooler) regions to tropical and sub-tropical (hotter) regions76. Temperature and precipitation remain the two major environmental factors affecting SOC concentration and stock within the complexity of land use change (LUC)-SOC distribution nexus77,78. In our study, MAP has more impact in terms of modulating SOC stock compared to MAT (See Fig. 6). This partly supports our second hypothesis that climate and land use history will serve as possible indicators to modulate the amount of change in SOC stocks.

Figure 6.

Figure 6

Linear relationship between soil carbon stock (Mg C/ha) and (A) mean annual precipitation (MAP); (B) and mean annual temperature (MAT); and total nitrogen stock (Mg N/ha) and (C) mean annual precipitation (MAP); (D) and mean annual temperature (MAT); (p ≤ 0.05, n = 16).

Figure 7.

Figure 7

Conceptual diagram summarizing factors and mechanisms driving SOC distribution under different land use types in semi-arid area of northern Ethiopia. The nutrient availability arrow illustrates the concentration pathway and distribution of SOC and TN contents across the land use types. The double-headed arrows indicates the direction of both MAT and %silt in modulating SOC distribution. The sizes of the pots simply refers to the “amount” of the SOC pools across land use types.

Another remarkable outlook in this study in terms of drivers of SOC distribution was provided by the clay fraction data on basis of occurrence or proportion. Thus, soils with high clay content recorded high SOC concentration and stock compared to soils with low clay content. This finding is in agreement with the work of67 in a study to assess the C:N ratios following land use change in Brazil.

In Cambisols of Hugumburda, Haikihelet and Geregera, the overall mean total sand fraction was high in natural (forest) and semi-natural (exclosure) ecosystems, with high proportions in sub-soil layers in most land use types excluding cropland at Geregera. This is in contrast with the findings of79 who reported high sand fraction in grazing land, followed by agroforestry and cropland in Nitosols of southern Ethiopia. In Vertisols of Desa’a, high clay fraction was observed in all the land use types with appreciable increase with depth. Differences in soil types and micro-climatic conditions might be responsible for these variations. Bockheim80, Ukaegbu et al.81 and Okolo et al.82 reported that soils formed on the same parent material within an ecological region are complexly linked to landscape and thus display substantial variations in soil properties. Furthermore, differences in BD was observed across locations in different land use types. Low BD in natural (forests) and semi-natural (exclosures) ecosystems, could be attributed to constant input of high soil organic residues on the upper layer of the soil8386. The contribution of tree roots to the subsoil organic matter (OM) accumulation, including root litter decomposition leads to the decrease in BD in forests8789.

Conclusions

The total SOC and TN concentrations and stocks were high in natural forest, intermediate in exclosure and grazing land, and low in croplands, and generally decreased with increasing depth in allland use types. Across soil depths and land use types, SOC and TN sequestration was higher in Cambisols than Vertisols, with clay content and MAP rather than C:N ratio alone being the most meaningful indices for SOC storage and soil quality assessment. Conversion of forest to cropland resulted to significant losses of SOC and TN with considerable amount of CO2 emission which contributes to change in climate. Exclosure establishment supported restoration of degraded grazing lands with recovery of SOC and TN stocks especially in the topsoil layer (Fig. 7). Thus, exclosure establishment could be a sustainable way to reverse soil fertility decline due to its C and N sequestration potentials. Additionally, more attention needs to be placed not only on the amount of SOC sequestration potential under different ecosystems and land use types in semi-arid area of northern Ethiopia, but also to ensure that they remain undisturbed for long periods of time, with mechanisms to detect differences before commencement of carbon trading schemes.

Acknowledgements

The scholarship support of Transdisciplinary Training for Resource Efficiency and Climate Change Adaptation in Africa (TRECC Africa II) to Chukwuebuka Christopher Okolo (CCO) is well acknowledged. We acknowledge the German Federal Ministry of Education and Research (BMBF) for the financial support given to Chukwuebuka Christopher Okolo (CCO) under the Green Talents—International Forum for High Potentials in Sustainable Development Program. Special thanks to the African-German Network of Excellence in Science (AGNES), BMBF and the Alexander von Humboldt Foundation (AvH) for the 2021 AGNES Grant for Junior Researchers granted to CCO. The final draft of the manuscript was initiated when the principal researcher was at Botswana International University of Science and Technology, Palapye, Botswana and completed when he was at Eberhard Karls University Tübingen Germany as a DAAD ClimapAfrica Postdoctoral Research Fellow.

Author contributions

C.C.O.: conceptualization, methodology, data curation, writing—review and editing. G.G.: conceptualization, supervision and methodology. A.Z.: supervision and project administration. M.H.: conceptualization, supervision and methodology. J.E.O.: writing—review and editing. C.B.O.: writing—review and editing. C.E.E.: data curation. E.E.: writing—review and editing. P.N.E.: writing—review and editing.

Data availability

The datasets used for this study are available from the corresponding author on reasonable request.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Lal R. Soil Carbon sequestration impacts on global climate change and food security. Science. 2004;30:1623–1627. doi: 10.1126/science.1097396. [DOI] [PubMed] [Google Scholar]
  • 2.Stockmann U, Adams MA, Crawford JW, Field DJ, Henakaarchchi MJ, Minasny B, McBratney AB, de Courcelles VDR, Singh K, Wheeler I, Abbott L, Angers DA, Baldock J, Bird M, Brookes PC, Chenu C, Jastrow JD, Lal R, Lehmann J, O’Donnel AG, Parton WJ, Whitehead D, Zimmerman M. The knowns, known unknowns and unknowns of sequestration of soil organic carbon. Agric. Ecosyst. Environ. 2013;164:80–99. doi: 10.1016/j.agee.2012.10.001. [DOI] [Google Scholar]
  • 3.Batjes NH. Total carbon and nitrogen in the soils of the world. Eur. J. Soil Sci. 1996;47(2):151–163. doi: 10.1111/j.1365-2389.1996.tb01386.x. [DOI] [Google Scholar]
  • 4.Michalzik B, Kalbitz K, Park JH, Solinger S, Matzner E. Fluxes and concentrations of dissolved organic carbon and nitrogen: A synthesis for temperate forests. Biogeochemistry. 2001;52:173–205. doi: 10.1023/A:1006441620810. [DOI] [Google Scholar]
  • 5.Malik AA, Martiny JBH, Brodie EL, et al. Defining trait-based microbial strategies with consequences for soil carbon cycling under climate change. ISME J. 2020;14:1–9. doi: 10.1038/s41396-019-0510-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Song MH, Guo Y, Yu FH, et al. Shifts in priming partly explain impacts of long-term nitrogen input in different chemical forms on soil organic carbon storage. Glob. Chang. Biol. 2018;24:4160–4172. doi: 10.1111/gcb.14304. [DOI] [PubMed] [Google Scholar]
  • 7.Okolo CC, Bore E, Gebresamuel G, Zenebe A, Mitiku H, Nwite JN, Dippold MA. Priming effect in semi-arid soils of northern Ethiopia under different land use types. Biogeochemistry. 2022 doi: 10.1007/s10533-022-00905-z. [DOI] [Google Scholar]
  • 8.Eze PN, Udeigwe TK, Stietiya MH. Distribution and potential source evaluation of heavy metals in prominent soils of Accra plains, Ghana. Geoderma. 2010;156(3–4):357–362. doi: 10.1016/j.geoderma.2010.02.032. [DOI] [Google Scholar]
  • 9.Eze PN, Mbakwe I, Okolo CC. Ecosystem functions of the soil highlighted in Igbo proverbs. In: Yang JE, Kirkham MB, Lal R, Huber S, editors. IUSS Global Soil Proverbs: Cultural Language of the Soil. Schweizerbart and Borntraeger Science Publishers; 2019. [Google Scholar]
  • 10.Nottingham AT, Bååth E, Reischke S, et al. Adaptation of soil microbial growth to temperature: Using a tropical elevation gradient to predict future changes. Glob. Chang. Biol. 2019;25:827–838. doi: 10.1111/gcb.14502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Paul KI, Polglase PJ, Nyakuengama JG, Khanna PK. Change in soil carbon following afforestation. Forest Ecol. Manag. 2002;168:241–257. doi: 10.1016/S0378-1127(01)00740-X. [DOI] [Google Scholar]
  • 12.Batjes NH. Options for increasing carbon sequestration in West Africa soils: An exploratory study with special focus on Senegal. Land Degrad. Dev. 2001;12:131–142. doi: 10.1002/ldr.444. [DOI] [Google Scholar]
  • 13.Powlson DS, Whitmore AP, Goulding KWT. Soil carbon sequestration to mitigate climate change: A critical re-examination to identify the true and the false. Eur. J. Soil Sci. 2011;62:42–55. doi: 10.1111/j.1365-2389.2010.01342.x. [DOI] [Google Scholar]
  • 14.Zhang K, Dang H, Zhang Q, Cheng X. Soil carbon dynamics following land-use change varied with temperature and precipitation gradients: Evidence from stable isotopes. Glob. Chang. Biol. 2015;21:2762–2772. doi: 10.1111/gcb.12886. [DOI] [PubMed] [Google Scholar]
  • 15.Gebresamuel G, Opazo-Salazar D, Corral-Núnez G, van Beek C, Elias E, Okolo CC. Nutrient Balance of farming systems in tigray, Northern Ethiopia. J. Soil Sci. Plant Nutr. 2021;21:315–328. doi: 10.1007/s42729-020-00362-3. [DOI] [Google Scholar]
  • 16.IPCC, Climate Change: The physical science basis. Contribution of working Group I to the Fourth Assessment. In Report of the Intergovernmental Panel on Climate Change (Eds. Solomon, S., Quin, D and Manning, M). (Cambridge University Press, Cambridge, UK) (2007).
  • 17.Yang YS, Xie JS, Sheng H. The impact of land use/cover change on storage and quality of soil organic carbon in mid-subtropical mountainous area of southern China. J. Geo. Sci. 2009;19:49–57. doi: 10.1007/s11442-009-0049-5. [DOI] [Google Scholar]
  • 18.Akinyemi FO, Tlhalerwa LT, Eze PN. Land degradation assessment in an African dryland context based on the composite Land Degradation Index and mapping method. Geocarto Int. 2021;36(16):1838–1854. doi: 10.1080/10106049.2019.1678673. [DOI] [Google Scholar]
  • 19.Button ES, Pett-Ridge J, Murphy DV, Kuzyakov Y, Chadwick DR, Jones DL. Deep-C storage: Biological, chemical and physical strategies to enhance carbon stocks in agricultural subsoils. Soil Biol. Biochem. 2022;170:108697. doi: 10.1016/j.soilbio.2022.108697. [DOI] [Google Scholar]
  • 20.Rumpel C, Kögel-Knabner I. Deep soil organic matter: A key but poorly understood component of terrestrial C cycle. Plant Soil. 2011;338(1):143–158. doi: 10.1007/s11104-010-0391-5. [DOI] [Google Scholar]
  • 21.Lal R, Lorenz K, Huttle RF, Schneider BU, Von BJ, et al. Terrestrial biosphere as a source and sink of atmospheric carbon dioxide. In: Lal R, et al., editors. Recarbonization of the Biosphere: Ecosystems and the Global Cycle. Springer; 2012. [Google Scholar]
  • 22.Shi Z, Allison SD, He Y, Levine PA, Hoyt AM, Beem-Miller J, Zhu Q, Wieder WR, Trumbore S, Randerson JT. The age distribution of global soil carbon inferred from radiocarbon measurements. Nat. Geosci. 2020;13:555–559. doi: 10.1038/s41561-020-0596-z. [DOI] [Google Scholar]
  • 23.Salome C, Nunan N, Pouteau V, Lerchw TZ, Chenu C. Carbon dynamics in topsoil and in subsoil may be controlled by different regulatory mechanisms. Glob. Chang. Biol. 2010;16:416–426. doi: 10.1111/j.1365-2486.2009.01884.x. [DOI] [Google Scholar]
  • 24.Sithole NJ, Magwaza LS, Thibaud GR. Long-term impact of no-till conservation agriculture and N-fertilizer on soil aggregate stability, infiltration and distribution of C in different size fractions. Soil Tillage Res. 2019;190:147–156. doi: 10.1016/j.still.2019.03.004. [DOI] [Google Scholar]
  • 25.Tashi S, Singh B, Keitel C, Adams M. Soil carbon and nitrogen stocks in forests along an altitudinal gradient in the eastern Himalayas and a meta-analysis of global data. Glob. Chang. Biol. 2016;22:2255–2268. doi: 10.1111/gcb.13234. [DOI] [PubMed] [Google Scholar]
  • 26.Zhou Z, Wang C, Luo Y. Effects of forest degradation on microbial communities and soil carbon cycling: A global meta-analysis. Global Ecol. Biogeography. 2018;27:110–124. doi: 10.1111/geb.12663. [DOI] [Google Scholar]
  • 27.Mhete M, Eze PN, Rahube TO, Akinyemi FO. Soil properties influence bacterial abundance and diversity under different land-use regimes in semi-arid environments. Sci. African. 2020;7:e00246. doi: 10.1016/j.sciaf.2019.e00246. [DOI] [Google Scholar]
  • 28.Walker TWN, Kaiser C, Strasser F, Herbold CW, Leblans NIW, Woebken D, Janssens IA, Sigurdsson BD, Richter A. Microbial temperature sensitivity and biomass change explain soil carbon loss with warming. Nat. Clim. Chang. 2018;8:885–889. doi: 10.1038/s41558-018-0259-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Murty D, Kirschbaum MUF, Mcmurtrie RE, Mcgilvray H. Does conversion of forest to agricultural land change soil carbon and nitrogen? A review of the literature. Glob. Chang. Biol. 2002;8:105–123. doi: 10.1046/j.1354-1013.2001.00459.x. [DOI] [Google Scholar]
  • 30.Veldkamp E, Schmidt M, Powers JS, Corre MD. Deforestation and reforestation impacts on soils in the tropics. Nat. Rev. Earth Environ. 2020;1:590–605. doi: 10.1038/s43017-020-0091-5. [DOI] [Google Scholar]
  • 31.Kebonye NM, Eze PN, Ahado SK, John K. Structural equation modeling of the interactions between trace elements and soil organic matter in semiarid soils. Intl. J. Environ. Sci. Technol. 2020;17(4):2205–2214. doi: 10.1007/s13762-019-02610-1. [DOI] [Google Scholar]
  • 32.Del Galdo L, Six J, Peressotti A, Cotrufo MF. Assessing the impact of land-use change on soil C sequestration in agricultural soils by means of organic matter fraction and stable C isotopes. Glob. Chang. Biol. 2003;9:1204–1213. doi: 10.1046/j.1365-2486.2003.00657.x. [DOI] [Google Scholar]
  • 33.Lal R. Carbon sequestration in dry land ecosystems of West Asia and North Africa. Land Degrad. Dev. 2002;13:45–59. doi: 10.1002/ldr.477. [DOI] [Google Scholar]
  • 34.Gebresamuel G, Singh BR, Mitiku H, Borresen T, Lal R. Carbon Stocks in Ethiopian Soils in relation to land use and soil management. Land Degrad. Dev. 2008;19(4):351–367. doi: 10.1002/ldr.844. [DOI] [Google Scholar]
  • 35.Fisseha I, Mats O, Karl S. Effect of land use changes on soil carbon status of some soil types in the Ethiopian Rift Valley. J. Drylands. 2011;4(1):289–299. [Google Scholar]
  • 36.Shiferaw A, Hans H, Gete Z. A review on soil carbon sequestration in Ethiopia to Mitigate land degradation and climate change. J. Environ. Earth Sci. 2013;3(12):187–201. [Google Scholar]
  • 37.Bazezew MN, Teshome S, Eyale B. Above- and below-ground reserved carbon in danaba community forest of Oromia Region, Ethiopia: Implications for CO2 emission balance. Am. J. Environ. Prot. 2015;4(2):75–82. [Google Scholar]
  • 38.Berihu T, Girmay G, Sebhatleab M, Berhane E, Zenebe A, Sigua GC. Soil carbon and nitrogen losses following deforestation in Ethiopia. Agron. Sust. Dev. 2017;37:1. doi: 10.1007/s13593-016-0408-4. [DOI] [Google Scholar]
  • 39.Gebresamuel G, Molla B, Teka K, Negash E, Haile M, Okolo CC. Changes in soil organic carbon stock and nutrient status after conversion of pasture land to cultivated land in semi-arid areas of northern Ethiopia. Arch. Agron. Soil Sci. 2022 doi: 10.1080/03650340.2020.1823372. [DOI] [Google Scholar]
  • 40.Hoyle FC, Baldock JA, Murphy DV. Soil organic carbon: Role in rainfed farming systems: With particular reference to Australian Conditions. In: Tow P, Cooper I, Partridge I, Birch C, editors. Rainfed Farming Systems. Springer; 2011. [Google Scholar]
  • 41.Mekuria W, Wondie M, Amare T, Wubet A, Feyisa T, Yitaferu B. Restoration of degraded landscapes for ecosystem services in North-Western Ethiopia. Heliyon. 2018;4:e00764. doi: 10.1016/j.heliyon.2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Okolo CC, Dippold MA, Gebresamuel G, Zenebe A, Haile M, Bore E. Assessing the sustainability of land use management of Northern Ethiopian drylands by various indicators for soil health. Ecol. Indic. 2020;112:106092. doi: 10.1016/j.ecolind.2020.106092. [DOI] [Google Scholar]
  • 43.WRB. International Union of Soil Science Working Group. In World Reference Base for Soil Resources 2014, update 2015 International soil classification system for naming soils and creating legends for soil maps. World Soil Resources Reports No. 106. FAO, Rome (2014).
  • 44.NMA 2018. National Metrological Agency (NMA), 2018. The National Metrological Agency of Ethiopia Mekelle center, Tigray Regional State, Mekelle, Ethiopia.
  • 45.Anikwe MAN, Obi ME, Agbim NN. Effect of crop and soil management practices soil compactibility in maize and groundnut plots in a Paleustult in Southeastern Nigeria. Plant Soils. 2003;253:457–465. doi: 10.1023/A:1024809608788. [DOI] [Google Scholar]
  • 46.Anikwe MAN. Carbon storage in soils of southeastern Nigeria under different management practices. Carbon Bal. Manag. 2010 doi: 10.1186/1750-0680-5-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.IPCC Guidelines for National Greenhouse Gas Inventories. In Vol. 4: Agriculture, Forestry and other Land Use (eds. Eggleston, S., Buendia, K., Miwa, K., Ngara, T. and Tanabe, K.) (Institute for Global Environmental Strategies, 2006).
  • 48.McKenzie, N., Ryan, P., Fogarty, P. & Wood, J. Sampling, measurement and analytical protocols for carbon estimation in soil, litter and coarse woody debris. National Carbon Accounting System Technical Report No. 14. Australian Greenhouse Office, Canberra (2000).
  • 49.Nelson, D. W. & Sommers, L. E. Total carbon, total organic carbon and organic matter. In Methods of Soil Analysis. Part 3: Chemical Methods. Agronomy Monograph No. 9 (Ed. Sparks, D.L) 961–1010. (American Society of Agronomy, 1996).
  • 50.Bremner JM, Mulvaney CS. Nitrogen-total. In: Keeney DR, Nelson DW, Page AL, editors. Chemical and Microbiological Properties. American Society of Agronomy and Soil Science Society of America; 1982. pp. 595–624. [Google Scholar]
  • 51.McLean, E. O. Soil pH and lime requirement. In Methods of Soil Analysis, Part 2: Chemical and Microbiological Properties. 2nd edn. Agronomy monograph No. 9 (Eds. Page, A.L., Miller, R.H and Keeney, D.R). 199–224. (American Society of Agronomy, 1982).
  • 52.Rhoades, J. D. Cation exchange capacity. In Methods of Soil Analysis: Part 2 Chemical and Microbial Properties. Agronomy Monograph No. 9. (Eds. Page, A.L., Miller, R.H and Keeney, D.R) pp. 149–157 (American Society of Agronomy, 1982).
  • 53.Blake, G. R. & Hartge, K. H. Bulk density. In Methods of Soil Analysis. Part 1: Physical and Mineralogical Properties. 2nd edn. Agronomy Monograph No. 9 (ed. Klute, A) 363–382. (American Society of Agronomy, 1986).
  • 54.Gee, G. W. & Bauder, J. W. Particle size analysis. In Methods of Soil Analysis. Part 1: Physical and Mineralogical Properties. 2nd edn. Agronomy Monograph No. 9. (Ed. A Klute) 91–100. (American Society of Agronomy, 1986).
  • 55.Gelaw AM, Singh BR, Lal R. Soil organic carbon and total nitrogen stocks under different land uses in a semi-arid watershed in Tigray, Northern Ethiopia. Agric. Ecosyst. Environ. 2014;188:256–263. doi: 10.1016/j.agee.2014.02.035. [DOI] [Google Scholar]
  • 56.Puget P, Lal R. Soil organic carbon and nitrogen in a Mollisol in Central Ohio as affected by tillage and land use. Soil Tillage Res. 2005;80:201–213. doi: 10.1016/j.still.2004.03.018. [DOI] [Google Scholar]
  • 57.Chan Y. Increasing soil organic carbon of agricultural land. Primefact. 2008;735:1–5. [Google Scholar]
  • 58.Worku G, Bantider A, Temesgen H. Effects of land use/land cover change on some soil physical and chemical properties in Ameleke micro-watershed Gedeo and Borena Zones. South Ethiopia. J. Environ. Earth Sci. 2014;4:13–24. [Google Scholar]
  • 59.Assefa D, Rewald B, Sanden H, Rosinger C, Abiyu A, Yitaferu B, Godbold DL. Deforestation and land use strongly effect soil organic carbon and nitrogen stock in Northwest Ethiopia. CATENA. 2017;153:89–99. doi: 10.1016/j.catena.2017.02.003. [DOI] [Google Scholar]
  • 60.Gessesse TA, Khamzina A, Gebresamuel G, Amelung W. Terrestrial carbon stocks following 15 years of integrated watershed management intervention in semi-arid Ethiopia. CATENA. 2020;190:104543. doi: 10.1016/j.catena.2020.104543. [DOI] [Google Scholar]
  • 61.Haileslassie A, Priess J, Veldkamp E, Teketay D, Lesschen JP. Assessment of soil nutrient depletion and its spatial variability on smallholders’ mixed farming systems in Ethiopia using partial versus full nutrient balances. Agric. Ecosyst. Environ. 2005;108:1–16. doi: 10.1016/j.agee.2004.12.010. [DOI] [Google Scholar]
  • 62.Lemenih M, Lemma B, Teketay D. Changes in soil carbon and total nitrogen following reforestation of previously cultivated land in the highlands of Ethiopia. Ethiopian J. Sci. 2005;28(2):99–108. [Google Scholar]
  • 63.Lemenih M, Karltun E, Olsson M. Soil organic matter dynamics after deforestation along a farm field chronosequences in southern highlands of Ethiopia. Agric. Ecosyst. Environ. 2005;109:9–19. doi: 10.1016/j.agee.2005.02.015. [DOI] [Google Scholar]
  • 64.Okebalama CB, Igwe CA, Okolo CC. Soil organic carbon levels in soils of contrasting land uses in Southeastern Nigeria. Trop. Subtrop. Agroecosyst. 2017;20:493–504. [Google Scholar]
  • 65.Nwite JN, Orji JE, Okolo CC. Effect of different land use systems on soil carbon storage and structural indices in Abakaliki, Nigeria. Indian J. Ecol. 2018;45(3):522–527. [Google Scholar]
  • 66.Don A, Schumacher J, Freibauer A. Impact of tropical land-use change on soil organic carbon stocks–a meta-analysis. Glob. Chang. Biol. 2011;17:1658–1670. doi: 10.1111/j.1365-2486.2010.02336.x. [DOI] [Google Scholar]
  • 67.Zinn YL, Marrenjo GJ, Silva CA. Soil C: N ratos are unresponsive to land use change in Brazil: A comparative analysis. Agric. Ecosyst. Environ. 2018;255:62–72. doi: 10.1016/j.agee.2017.12.019. [DOI] [Google Scholar]
  • 68.Lou YL, Xu MG, Chen XN, He XH, Zhao K. Stratification of soil organic C, N and C: N ratio as affected by conservation tillage in two maize fields of China. CATENA. 2012;95:124–130. doi: 10.1016/j.catena.2012.02.009. [DOI] [Google Scholar]
  • 69.Xiao X, Kuang X, Sauer TJ, Heitman JL, Horton R. Bare soil carbon dioxide fluxes with time and depth determined by high-resolution gradient-based measurements and surface chambers. Soil Sci. Soc. Am. 2015;79:1073–1083. doi: 10.2136/sssaj2015.02.0079. [DOI] [Google Scholar]
  • 70.Wang X, Fu S, Li J, Zou X, Zhang W, Xia H, Lin Y, Tian Q, Zhou L. Forest soil profile inversion and mixing change the vertical stratification of soil CO2 concentration without altering soil surface CO2 Flux. Forests. 2019;10:192. doi: 10.3390/f10020192. [DOI] [Google Scholar]
  • 71.Bates CT, Escalas A, Kuang J, Hale L, Wang Y, Herman D, Nuccio EE, Wan X, Bhattacharyya A, Fu Y, Tian R. Conversion of marginal land into switchgrass conditionally accrues soil carbon but reduces methane consumption. ISME J. 2021;16:10. doi: 10.1038/s41396-021-00916-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Slessarev EW, Nuccio EE, McFarlane KJ, Ramon CE, Saha M, Firestone MK, Pett-Ridge J. Quantifying the effects of switchgrass (Panicum virgatum) on deep organic C stocks using natural abundance 14C in three marginal soils. GCB Bioenergy. 2020;12:834–847. doi: 10.1111/gcbb.12729. [DOI] [Google Scholar]
  • 73.Balesdent J, Besnard E, Arrouays D, Chenu C. The dynamics of carbon in particle size fractions of soil in a forest-cultivation sequence. Plant Soil. 1998;201:49–57. doi: 10.1023/A:1004337314970. [DOI] [Google Scholar]
  • 74.Birch HF, Friend MT. The organ matter and nitrogen status of east African soils. J. Soil Sci. 1956;7:156–167. doi: 10.1111/j.1365-2389.1956.tb00871.x. [DOI] [Google Scholar]
  • 75.Deng L, Zhu G, Tang Z, Shangguan Z. Global patterns of the effects of land-usechanges on soil carbon stocks. Glob. Ecol. Conserv. 2016;5:127–138. doi: 10.1016/j.gecco.2015.12.004. [DOI] [Google Scholar]
  • 76.Post WM, Kwon KC. Soil carbon sequestration and land-use change: Processes and potential. Glob. Chang. Biol. 2000;6:317–327. doi: 10.1046/j.1365-2486.2000.00308.x. [DOI] [Google Scholar]
  • 77.Feng X, Simpson MJ. Temperature responses of individual soil organic matter components. J. Geophys. Res. Biogeosci. 2008 doi: 10.1029/2008JG000743. [DOI] [Google Scholar]
  • 78.Chen S, Huang Y, Zou J, Shi Y. Mean residence time of global topsoil organic carbon depends on temperature, precipitation and soil nitrogen. Glob. Planet. Chang. 2013;100:99–108. doi: 10.1016/j.gloplacha.2012.10.006. [DOI] [Google Scholar]
  • 79.Alemayehu K, Sheleme B. Effects of different land use systems on selected soi properties in South Ethiopia. J. Soil Sci. Environ. Manag. 2013;4(5):100–107. doi: 10.5897/JSSEM2013.0380. [DOI] [Google Scholar]
  • 80.Bockheim JG. Soil endemism and its relation to soil formation theory. Geoderma. 2005;129:109–124. doi: 10.1016/j.geoderma.2004.12.044. [DOI] [Google Scholar]
  • 81.Ukaegbu EP, Osuaku SK, Okolo CC. Suitability assessment of soils supporting oilpalm plantations in the coastal plains sand, Imo State Nigeria. Int. J. Agric. For. 2015;5(2):113–120. [Google Scholar]
  • 82.Okolo CC, Akamigbo FOR, Ezeaku PI, Nwite JN, Nwite JC, Ezeudo VC, Ene J, Ukaegbu EP, Udegbunam ON, Eze NC. Impact of open cast mine land use on soil physical properties in Enyigba, Southeastern Nigeria and the implication for sustainable land use management. Niger. J. Soil Sci. 2015;25(1):95–101. [Google Scholar]
  • 83.Nwite JN, Okolo CC. Soil water relations of an Ultisol amended with agro-wastes and its effect on grain yield of maize (Zea Mays L.) in Abakaliki, Southeastern Nigeria. Eur. J. Sci. Res. 2016;141:126–140. [Google Scholar]
  • 84.Nwite JN, Okolo CC. Organic carbon dynamics and changes in some physical properties of soil and their effect on grain yield of maize under conservative tillage practices in Abakaliki, Nigeria. Afr. J. Agric. Res. 2017;12(26):2215–2222. doi: 10.5897/AJAR2017.12333. [DOI] [Google Scholar]
  • 85.Mbah CN, Njoku C, Okolo CC, Attoe E, Osakwe UC. Amelioration of a degraded Ultisol with hardwood biochar: Effects on soil physico-chemical properties and yield of cucumber (Cucumis sativus L) Afr. J. Agric. Res. 2017;12(21):1781–1792. doi: 10.5897/AJAR2016.11654. [DOI] [Google Scholar]
  • 86.Nandan R, Singh V, Singh SS, Kumar V, Hazra KK, Nath CP, Poonia S, Kanwar Malik R, Bhattacharyya R, McDonald A. Impact of conservation tillage in rice–based cropping systems on soil aggregation, carbon pools and nutrients. Geoderma. 2019;340:104–114. doi: 10.1016/j.geoderma.2019.01.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Sharma, K.L. Effect of agroforestry systems on soil quality–monitoring and assessment. Central Research Institute for Dryland Agriculture. 2011. http://www.crida.in/DRM1-WinterSchool/KLS.pdf/. Accessed on 30 Dec 2018.
  • 88.Okolo CC, Gebresamuel G, Zenebe A, Haile M, Eze PN. Accumulation of organic carbon in various soil aggregate sizes under different land use systems in a semi-arid environment. Agric. Ecosyst. Environ. 2020;297:106924. doi: 10.1016/j.agee.2020.106924. [DOI] [Google Scholar]
  • 89.Okolo CC, Gebresamuel G, Retta AN, Zenebe A, Haile M. Advances in quantifying soil organic carbon under different land uses in Ethiopia: A review and synthesis. Bull. Natl. Res. Cent. 2019;43(99):2019. doi: 10.1186/s42269-019-0120-z. [DOI] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used for this study are available from the corresponding author on reasonable request.


Articles from Scientific Reports are provided here courtesy of Nature Publishing Group

RESOURCES