Previous Article in Journal
Two-Stage Detection Algorithm for Plum Leaf Disease and Severity Assessment Based on Deep Learning
Previous Article in Special Issue
Digestate from an Agricultural Biogas Plant as a Factor Shaping Soil Properties
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effects of Incubation Temperature and Sludge Addition on Soil Organic Carbon and Nitrogen Mineralization Characteristics in Degraded Grassland Soil

1
State Key Laboratory of Eco-Hydraulics in Northwest Arid Region, Xi’an University of Technology, NO. 5 South Jinhua Road, Xi’an 710048, China
2
Key Laboratory of Natural Resource Element Coupling and Effects, Ministry of Natural Resources, Natural Resources and Earth System Science, Beijing 100055, China
3
Northwest Surveying and Planning Institute of National Forestry and Grassland Administration, Xi’an 710048, China
*
Author to whom correspondence should be addressed.
Agronomy 2024, 14(7), 1590; https://doi.org/10.3390/agronomy14071590 (registering DOI)
Submission received: 14 June 2024 / Revised: 18 July 2024 / Accepted: 18 July 2024 / Published: 21 July 2024

Abstract

:
Elucidating the characteristics and underlying mechanisms of soil organic carbon (SOC) and nitrogen mineralization in the context of sludge addition is vital for enhancing soil quality and augmenting the carbon sink capacity of soil. This study examined the chemical properties, enzyme dynamics, and organic carbon and nitrogen mineralization processes of soil from degraded grasslands on the Loess Plateau at various incubation temperatures (5, 15, 25, and 35 °C) and sludge addition rates (0%, 5.0%, 10.0%, and 20.0%) through a laboratory incubation experiment. The results showed that incubation temperature, sludge addition, and their interactive effects significantly altered the soil enzyme C:N, C:P, and N:P stoichiometries. The cumulative mineralization rates of SOC and nitrogen increased significantly with increasing incubation temperature and sludge addition rate. Principal component analysis revealed a significant linear correlation between cumulative SOC and nitrogen mineralization. Random forest analysis indicated that β-1,4-Glucosidase (BG), β-1,4-N-acetyglucosaminidase (NAG), cellobiohydrolase (CBH), ammonium nitrogen (NO3), enzyme C:P ratio, alkaline phosphatase (ALP), and incubation temperature were crucial determinants of cumulative SOC mineralization. Structural equation modeling demonstrated that sludge addition, NO3, NAG, ALP, and enzyme C:P positively impacted SOC mineralization, whereas dissolved organic carbon and BG had negative impacts. Conversely, incubation temperature negatively affected soil nitrogen mineralization, whereas NO3, available phosphorus, and ALP contributed positively. Sludge addition and temperature indirectly modulated soil net nitrogen mineralization by altering soil chemical properties and enzyme activities. These findings underscore the role of SOC and nitrogen mineralization as indicators for evaluating soil nutrient retention capabilities.

1. Introduction

Soil degradation is a critical global environmental challenge [1]. The acceleration of soil degradation due to climate change and anthropogenic pressures has reduced agricultural yields, caused biodiversity loss, and diminished ecosystem services [2]. Urbanization and economic growth have led to a substantial increase in the generation of municipal sewage sludge [3]. Sewage sludge, enriched with essential nutrients, such as carbon, nitrogen, and phosphorus, offers a promising avenue for improving soil structure and fertility, thereby contributing to soil restoration and sustainable waste management [4]. The dynamic processes of soil organic carbon (SOC) and nitrogen mineralization play pivotal roles in the biogeochemical cycles of terrestrial ecosystems. However, the complex interplay between global warming and soil organic matter mineralization complicates the creation of predictive models of soil carbon and nutrient dynamics [5]. Thus, to optimize strategies for nutrient sequestration and enhance soil health, expansive research is required to elucidate the synergistic effects of sludge application and temperature fluctuations on SOC stability and nutrient cycling.
Studies have evaluated the impacts of sludge addition and temperature on soil chemical properties and enzymatic activities [6,7]. The application of sludge to soil matrices significantly modifies soil physicochemical properties, microbial community structure, and diversity. Sastre-Conde et al. [8] demonstrated that composted sewage sludge effectively restored saline-degraded soils, markedly improving plant germination rates and optimizing the cation balance and organic matter content. Similarly, Yue et al. [9] reported that sludge application in unfertilized urban green spaces finely tuned soil nutrient configurations, thereby fostering vegetative growth. Ahmad et al. [10] noted that sludge addition improved soil nutrient levels and microbial and plant biomass and facilitated the sustainable management of solid waste, contributing to reduced greenhouse gas emissions and enhanced nutrient recycling. Geng et al. [11] found that sludge addition markedly increased soil enzyme activity and alleviated carbon and nitrogen constraints within the soil. In a related study, Geng et al. [12] observed that elevated temperatures accelerated the breakdown of total nitrogen and significantly increased the available nitrogen content in Tibetan highland soils. Soil enzyme activity and temperature are positively correlated, with rising temperatures enhancing the enzymatic function [13,14,15]. Xiao et al. [16] highlighted that soil ecological stoichiometry, which explores the dynamics of various soil chemical elements, is pivotal for understanding ecological interactions and determined that changes in rhizosphere enzyme activity could dictate nutrient dynamics and plant succession patterns. Furthermore, Tan et al. [17] noted that increased temperatures reduced soil carbon-to-phosphorus and nitrogen-to-phosphorus ratios more rapidly than phosphorus alone, thereby hastening the depletion of soil organic matter. Overall, these findings underscore the beneficial role of sludge in augmenting soil nutrient frameworks and enzymatic activity, thereby enriching overall soil health and fertility.
The influences of temperature and sludge addition on the mineralization dynamics of SOC and nitrogen are highly complex [18]. Within the framework of global warming, elevated temperatures are likely to expedite SOC decomposition, thereby augmenting atmospheric carbon dioxide levels and contributing to a positive feedback mechanism in climate warming [19]. The mineralization of SOC and nitrogen constitutes a fundamental process in the decomposition of soil organic matter, profoundly affecting the structural integrity and functional dynamics of terrestrial ecosystems. Pérez-Lomas et al. [20] conducted a detailed investigation of the effects of applying composite compost on the organic carbon profiles of four Mediterranean agricultural soils. Their findings indicated that the incorporation of composite compost markedly enhanced the mineralization rates of SOC, especially in soils characterized by inherently low organic carbon levels. Zhang et al. [21] endeavored to improve soil quality by treating diverse wastes via sludge composting and exploring the equilibrium between the accumulation and degradation of SOC in amended soils. They found that increasing the proportion of composted inputs notably augmented soil respiration and carbon mineralization rates, although municipal sludge compost proved to be more effective as a plant fertilizer. In a three-year field study, Chen et al. [22] observed that biochar-induced competitive interactions among predominant microbial groups significantly fostered bacterial and fungal diversity, consequently diminishing the mineralization of SOC. Ribbons et al. [23] conducted a comprehensive analysis of microbial communities, functionalities, and nitrogen cycling dynamics within four distinct forest soils and determined that fluctuations in soil enzyme activity profoundly influence net nitrogen mineralization. In a comprehensive review of climate dynamics and plant-specific nitrogen preferences, Zhang et al. [24] discovered that net nitrogen mineralization rates in humid climates substantially exceeded those in semi-arid and arid regions, underscoring a profound linkage between nitrogen mineralization processes and climatic conditions. Wang et al. [25] studied the synergistic effects between soil organic matter and minerals across varied topographical gradients and detailed how long-term climatic conditions sculpt soil attributes. They highlighted that the processes of SOC and nitrogen mineralization are predominantly governed by climatic variables and the composition of soil organic matter. However, the intrinsic associations and interactive mechanisms underlying the mineralization processes of SOC and nitrogen remain only partially understood, necessitating more exhaustive investigative efforts.
The Loess Plateau of China is a dry and semi-arid region characterized by an exceptionally fragile ecological environment. Prolonged and improper pastoral and agricultural practices, coupled with unsuitable land use, have led to intense soil erosion and aggravated land degradation [26]. The loess soils on the Loess Plateau are characterized by low organic matter content and inadequate nitrogen and phosphorus levels, which, along with notable daily temperature fluctuations, substantially influence the quality of vegetation restoration [27]. However, despite the high nutrient content of sludge, there is a dearth of research exploring its impact as a soil amendment in loess areas. Therefore, this study evaluated the effects of sludge addition and incubation temperature on the dynamics of SOC and nitrogen mineralization in degraded grassland soils sampled from the Loess Plateau. The hypotheses of this study were as follows: (1) Different temperatures and sludge additions significantly affect soil chemical properties, enzyme activities, and ecological stoichiometry. (2) Elevated temperature has a stronger effect on soil carbon and nitrogen mineralization than that of sludge addition. (3) A level of synergy exists between net soil carbon mineralization and net nitrogen mineralization. The findings of this study are expected to offer a robust theoretical foundation for both restoration of degraded soils on the Loess Plateau and strategic planning of municipal sludge disposal.

2. Materials and Methods

2.1. Soil and Sludge Samples

Soil samples were collected from the top 20 cm layer of degraded grasslands within the Wangmaogou watershed in Shaanxi Province, China, and were sieved through a 2 mm mesh to exclude litter and roots. This region has a continental monsoon climate, with an average annual precipitation of 513 mm and average temperature of 10.2 °C. This region is situated on the northern Loess Plateau and is dominated by loess soil. The low organic matter content of this soil contributes significantly to extensive soil erosion and creates a delicately fragile ecosystem. The chemical properties of the soil samples are listed in Table 1.
Sludge samples were collected from a wastewater treatment facility in Xi’an, China. The collected sludge was aerobically composted within an experimental hall and allowed to mature naturally, yielding dry composted sludge. The main chemical characteristics of the dry sludge are listed in Table 1. The dry sludge was pulverized, passed through a 2 mm mesh, and mixed with soil samples to conduct mineralization incubation experiments.

2.2. Experimental Design

The experimental design included four sludge addition levels and four incubation temperatures, resulting in 16 treatment configurations. The soil samples were homogeneously blended with sludge at ratios of 0.0%, 5.0%, 10.0%, and 20.0% dry weight (labeled CK, S5, S10, and S20, respectively). Each 60.0 g aliquot of the blended soil sample was carefully allocated into 250 mL culture bottles, maintaining the soil moisture content at approximately 60% of its field capacity to optimize the conditions for microbial activity. Prior to the main incubation phase, the bottles underwent a 7-day pre-incubation at a constant 25 °C to catalyze and stabilize microbial activity within the soil matrix. Following this initial phase, the bottles were subject to a 50-day incubation period at temperatures of 5, 15, 25, and 35 °C. Soil moisture levels within the culture bottles were maintained at approximately 60% of the field capacity throughout the incubation period by employing a gravimetric method for precise hydration control every two days.

2.3. Soil Carbon and Nitrogen Mineralization Determination

To measure net carbon (Net-C) mineralization, gas samples were collected on days 1, 3, 7, 10, 15, 20, 25, 30, 35, 40, 45, and 50 to monitor the progression of carbon mineralization. Prior to gas sample collection, the culture bottle was hermetically sealed using a rubber stopper, followed by the injection of 30 mL of fresh air to ensure a consistent testing environment. The injected air was mixed thoroughly, and a 30 mL sample of the equilibrated gas mixture was withdrawn from the culture bottle and transferred into a vacuum gas collection bottle. The culture bottle was resealed and placed in a constant temperature incubator for 8 h, after which a second gas collection was performed. The concentration of CO2 in both gas samples was quantified using a gas chromatograph (Agilent 7890A; Agilent Technologies, Santa Clara, CA, USA).
The rate of SOC mineralization was determined using Equation (1), written as follows:
R c = β × V m × 1 C × Δ c Δ t × 273 273 + T × α
where Rc: SOC mineralization rate (mgC·g−1·SOC·d−1); “β”: conversion coefficient for CO2 gas to standard units, 1.964 (kg·m3); V: total gas volume inside the culture bottle (m3); m: dry mass of the sample in the culture bottle (kg); C: organic carbon content of each sample (g·kg−1); Δc: change in CO2 concentration over the incubation period (mg·kg−1); ΔT: incubation time (d); T: incubation temperature (°C); and α: mass conversion coefficient for converting CO2 to C, 12/44.
The cumulative Net-C mineralization was calculated according to Equation (2), written as follows:
N e t - C = i = 1 n 1 R i × T i
where Net-C: unit organic carbon cumulative mineralization (mg·g−1·SOC−1); i: index number for the measurement occasion; n: total number of measurements; Ri: average organic carbon mineralization rate between two sampling times (mg·g−1·SOC·d−1); and Ti: number of days between these intervals (d).
To measure net nitrogen (Net-N) mineralization, destructive sampling was conducted on days 1, 3, 7, 15, 25, 35, and 50 of incubation, with each sampling consisting of three replicates, resulting in 336 samples. Soil ammonium nitrogen (NH4+) and nitrate nitrogen (NO3) contents were determined using a fully automated discrete chemical analyzer with flow injection analysis [28]. The net nitrogen mineralization rate was calculated using Equation (3).
R N = 1 C × N H 4 + N t 2 + N O 3 N t 2 N H 4 + N t 1 + N O 3 N t 1 t 2 t 1
where RN: net nitrogen mineralization rate between times t1 and t2 (mg·g−1·SOC−1·d−1); C: organic carbon content of each sample (g·kg−1); (NH4+)t2 and (NO3)t2: ammonium nitrogen and nitrate nitrogen content in the soil at time t2, respectively (mg·kg−1); and (NH4+)t1 and (NO3)t1: ammonium nitrogen and nitrate nitrogen content in the soil at time t1, respectively (mg·kg−1).
The cumulative Net-N mineralization was calculated according to Equation (4), written as follows:
N e t - N = i = 1 n 1 R i × T i
where Net-N: unit organic carbon cumulative mineralization (mg·g−1·SOC−1); i: index number for the measurement occasion; n: total number of measurements; Ri: average net nitrogen mineralization rate between two sampling times (mg·g−1·SOC·d−1); and Ti: number of days between these intervals (d).

2.4. Soil Nutrients and Enzyme Activity Determination

Following a 50-day incubation period, SOC, dissolved organic carbon (DOC), total nitrogen (TN), total phosphorus (TP), available phosphorus (AP), β-1,4-Glucosidase (BG), cellulobiohydrolase (CBH), β-1,4-N-acetyglucosaminidase (NAG), and alkaline phosphatase (ALP) were quantified. SOC concentrations were determined using the dichromate oxidation–ferrous sulfate titration method. Soil NH4+, NO3, TP, and AP concentrations were determined using an automated discontinuous chemical analyzer (Clever Chem 200, Germany). Soil TN concentrations were determined using a Foss 8400 automatic Kjeldahl nitrogen analyzer. The stoichiometric ratios of the SOC to nitrogen (C:N), carbon to phosphorus (C:P), and nitrogen to phosphorus (N:P) were calculated as SOC:TN, SOC:TP, and TN:TP, respectively.
The potential activities of four soil enzymes associated with soil carbon (C), nitrogen (N), and phosphorus (P) cycling were assayed. Soil BG and CBH enzymes facilitate carbon acquisition; soil NAG catalyzes nitrogen acquisition; and soil ALP promotes phosphorus acquisition. The different soil enzyme functions and the substrates required are shown in Table 2. Enzymatic activity was determined using a 96-well plate fluorometric assay, following the protocol outlined by Saiya-Cork et al. [29]. Enzyme activities were standardized against SOC concentration, with the results expressed as nmol·h−1·g−1·SOC−1. The logarithmic ratios of soil enzyme activities were calculated as ln(BG + CBH):ln(NAG), ln(BG + CBH):ln(ALP), and ln(NAG):ln(ALP) [30].

2.5. Statistical Analysis

A two-way analysis of variance was used to assess the influence of incubation temperature, sludge addition, and their interactive effects on soil chemical properties, enzyme activities, and stoichiometric ratios. Means were compared using Duncan’s multiple range test for detailed analysis. Principal component analysis (PCA) was conducted to elucidate the similarities in soil chemical properties, enzyme activities, and cumulative mineralization across various treatments. Correlation analysis delineated the associations among soil chemical properties, enzyme activities, and cumulative mineralization rates. A random forest model quantitatively identified the key predictors influencing the cumulative mineralization of net soil organic carbon and nitrogen. The significance of the model and its predictors were validated using the A3 and rfPermute packages [31]. A structural equation model (SEM) was constructed to elucidate the direct and indirect influences of significant predictors on the cumulative mineralization of net soil organic carbon and nitrogen. The model fit was evaluated using a non-significant chi-square test (p > 0.05), goodness of fit index (GFI), and root mean square error of approximation. The PCA, random forest model, and SEM were implemented using the Vegan, randomForest, lavaan, and ggplot 2 packages in R [32,33].

3. Results

3.1. Soil Chemical Properties

The incubation temperature significantly influenced the concentrations of SOC, DOC, NH4+, NO3, and AP (Figure 1) (p < 0.05, p < 0.01, p < 0.001). With increasing incubation temperature, there was a significant reduction in SOC and NH4+ concentrations. Specifically, compared to the concentrations at 5 °C, at 15 to 35 °C, the SOC concentration declined by 1.64% to 4.93% and the NH4+ concentration declined by 5.43% to 24.42%, respectively. The concentrations of DOC and NO3 escalated significantly as the incubation temperature increased. Compared to at 5 °C, at 15 to 35 °C, the DOC concentration increased by 3.19% to 13.23% and the NO3 concentration increased by 101.57% to 285.22%. The content of soil AP increased significantly with increasing temperature, showing notable increases of 5.44 to 10.65% under incubation temperatures of 15 °C to 35 °C compared with that at 5 °C.
Sludge addition significantly influenced the concentrations of SOC, TN, TP, DOC, NH4+, NO3, and AP in the soil (Figure 1) (p < 0.001). The concentrations of SOC, TN, TP, and NH4+ increased markedly with increasing proportions of sludge, peaking under S20. Relative to the control (CK), the SOC, TN, and TP levels under S5 to S20 increased 233% to 932%, 2.78% to 911%, and 149% to 689%, respectively, whereas the NH4+ levels increased by 16.49% to 35.35%. The most notable increase in soil DOC content occurred under S10, with significant increases ranging from 69.79% to 96.26% under S5 to S20, relative to CK. Under S5 to S20, NO3 and AP concentrations in the soil increased by 13.08% to 55.96% for NO3 and 78.17% to 150.02% for AP relative to CK, with the most substantial enhancements under S5. Furthermore, the interaction between sludge addition and temperature significantly influenced the concentrations of DOC, NH4+, NO3, and AP (p < 0.05 or p < 0.001).

3.2. Soil Enzyme Activities

The incubation temperature, sludge addition, and their combined effects markedly influenced the activities of soil enzymes, such as CBH, BG, NAG, and ALP (Figure 2) (p < 0.001). The enzymatic activities of CBH, BG, NAG, and ALP significantly increased with increasing incubation temperature. Relative to the baseline at 5 °C, enzyme activities at temperatures from 15 to 35 °C exhibited substantial elevations: CBH (81.35% to 426.68%), BG (80.03% to 225.80%), NAG (95.49% to 215.10%), and ALP (116.91% to 204.61%). Likewise, relative to the CK, under S5 to S20, the activities of CBH (47.72% to 54.18%), BG (71.55% to 91.81%), NAG (69.59% to 128.33%), and ALP (13.75% to 17.49%) notably increased.

3.3. Stoichiometric Characteristics of Soil Chemical Properties and Enzyme Activities

The addition of sludge significantly influenced the soil C:N, C:P, and N:P ratios (Figure 3) (p < 0.001). The soil C:N ratio exhibited a notable reduction, ranging from 11.81% to 17.57% under S5 to S20 relative to the CK, correlating with the increased proportions of sludge addition. Concurrently, the soil C:P and N:P ratios significantly increased, increasing by 26.19% to 34.06% and 49.70% to 58.48%, respectively, under S5 to S20 compared with the CK.
The incubation temperature, sludge addition, and their interactions had pronounced impacts on the ratios of soil enzymes C:N, C:P, and N:P (Figure 3) (p < 0.001). The soil enzyme C:N ratio notably decreased from 8.30% to 11.35% with increasing temperature from 15 to 35 °C relative to that at 5 °C. Correspondingly, soil enzyme C:P and N:P ratios significantly increased, with increases of 2.91% to 18.12% and 9.69% to 23.24%, respectively. Compared with CK, the soil enzyme C:N decreased significantly with increasing sludge addition ratio, with those of the S5 to S20 treatment groups decreasing by 14.77 to 21.01%, respectively. Concurrently, the soil enzyme C:P and N:P ratios underwent substantial enhancements, increasing from 18.14% to 24.08% and 32.71% to 50.39%, respectively, under S5 to S20 relative to CK.

3.4. SOC and Nitrogen Mineralization Characteristics

The interaction effects of incubation temperature and sludge addition profoundly modulated the cumulative mineralization rates of net SOC and nitrogen (Figure 4) (p < 0.001). With increasing incubation temperature, there was a marked increase in the cumulative mineralization rates of both net SOC and nitrogen. Relative to the baseline at 5 °C, the mineralization rates for net carbon and net nitrogen at 15 to 35 °C increased from 171.64% to 429.48% and 208.22% to 542.30%, respectively. Sludge addition proportionally increased the cumulative mineralization rates of net carbon and net nitrogen in the soil. Compared to the CK, the treatment groups with 5% to 20% sludge addition exhibited increased mineralization rates of net carbon (125.85% to 151.10%) and net nitrogen (19.61% to 89.50%). There was a significant linear correlation between the cumulative mineralization rates of net carbon and net nitrogen in the soil (Figure 5c). Among the various incubation temperatures, a significant linear correlation between the cumulative mineralization of net carbon and net nitrogen was observed at 25 °C (Figure 5b). Across varying proportions of sludge, a consistent and significant linear correlation was found between the cumulative mineralization rates of net organic carbon and nitrogen (Figure 5a).

3.5. Factors Impacting the Variation of SOC and Nitrogen Mineralization

PCA elucidated pronounced variations in soil chemical properties, enzyme activities, ecological stoichiometric ratios, and cumulative mineralization of SOC and nitrogen across different incubation temperatures and sludge additions (Figure 6). PC1 and PC2 explained 53.28% and 26.63% of the total variance in soil properties, respectively. Notable disparities in soil chemical properties, enzyme activities, ecological stoichiometric ratios, and rates of cumulative carbon and nitrogen mineralization were observed under S5, S10, and S20 across the PC1 and PC2 axes. Additionally, marked variations were apparent in soil chemical properties, enzyme activities, ecological stoichiometric ratios, and the cumulative mineralization of carbon and nitrogen at incubation temperatures of 15, 25, and 35 °C along the PC1 and PC2 axes.
Soil nutrient content, enzyme activity, ecological stoichiometry, and cumulative mineralization of net SOC and nitrogen under different incubation temperatures and sludge additions were significantly correlated (Figure 7) (p < 0.05, p < 0.01, or p < 0.001). This coincides with Hypothesis (1). Cumulative net carbon mineralization in the soil exhibited strong positive correlations with incubation temperature, sludge addition, SOC, TN, TP, DOC, NO3, AP, CBH, BG, NAG, ALP, soil N:P, enzyme C:P, and enzyme N:P, while showing significant negative correlations with soil C:N and enzyme C:N. Similarly, cumulative net nitrogen mineralization in the soil displayed marked positive correlations with incubation temperature, DOC, NO3, AP, and soil enzymatic activities, while it was inversely associated with NH4+ and soil C:N.
A random forest model was employed to quantitatively determine the key predictors influencing the cumulative mineralization of net SOC and nitrogen (Figure 8). Incubation temperature, sludge addition, DOC, NO3, CBH, BG, NAG, ALP, and enzyme C:P ratio were identified as critical predictors of soil net carbon mineralization, while incubation temperature, sludge addition, TP, NO3, AP, CBH, BG, NAG, ALP, and enzyme C:P ratio were crucial predictors of soil net nitrogen mineralization. A SEM was applied to elucidate the direct, indirect, and total effect contributions of the pivotal predictors to the cumulative mineralization of net SOC and nitrogen (Figure 9). Sludge addition, NO3, NAG, ALP, and enzyme C:P ratio exerted direct positive influences on net SOC mineralization, whereas DOC and BG had direct negative impacts. Conversely, sludge addition and incubation temperature indirectly modulated net SOC mineralization via alterations in soil chemical properties and enzymatic activities. Temperature, NO3, AP, and ALP had a direct positive effect on net cumulative soil N mineralization. The total effects of incubation temperature on soil net cumulative carbon mineralization (0.666) and net cumulative nitrogen mineralization (0.587) were greater than those of sludge addition (0.311 and 0.229) (Table 3 and Table 4). Furthermore, NO3 was the main factor affecting soil net cumulative carbon and nitrogen mineralization.

4. Discussion

4.1. Soil Nutrients and Enzyme Activity

Soil is the foundational source of nutrients for plant growth, and the status of soil nutrients is pivotal for effective soil remediation [34]. The application of sludge in soil remediation significantly improves soil structure and increases soil nutrient contents [22]. We observed a respective decline and marked increase in soil NH4+ and NO3 contents with increasing temperature, which is consistent with the findings of Hu et al. [35] regarding the transformation dynamics of TN in soils. This result evidenced that the nitrification process is stronger than the ammonification process in the mineralization of soil TN. Soil DOC and AP concentrations increased significantly with increasing temperature, corroborating the findings of Song et al. [36], who posited that elevated temperatures intensify the breakdown of total soil nutrients, thereby boosting nutrient availability. Lehtinen et al. [37] and Jakubus et al. [38] demonstrated that the use of sewage sludge compost substantially enhanced the concentrations of SOC, TN, phosphorus, and K, establishing sludge as a sustainable fertilizer that concurrently retards the nutrient decomposition process in soils. These results align with our observations that the SOC, TN, and TP concentrations progressively increased with increasing gradients of sludge addition. Furthermore, our data demonstrated that key soil efficacy indicators, including DOC, NH4+, NO3, and AP, initially surged and subsequently plateaued with increasing sludge addition rates, which is consistent with the findings of De Lucia et al. [39] and Elsalam et al. [40]. This suggests that the incorporation of composted sludge can rapidly augment the availability of soil nutrients, thereby mitigating the environmental impacts associated with organic waste management.
Soil enzymes are pivotal in facilitating the cycling of carbon and nutrients in terrestrial ecosystems [41]. These enzymes are integral to biogeochemical cycling and the transformation of carbon, nitrogen, and phosphorus in soil ecosystems. Temperature modulates the synthesis of soil enzymes by regulating microbial activity, thereby exerting a profound effect on the mineralization of soil organic matter [42,43]. This study found that the activities of the enzymes CBH, BG, NAG, and ALP increased with increasing temperature, corroborating the observations of Meng et al. [44] on soil enzyme responses to global warming, suggesting that elevated temperatures boost enzyme activity [45]. Skońska et al. [46] demonstrated through both laboratory and field studies that sludge application markedly enhanced soil carbon and nitrogen levels and enzymatic activities. Additionally, our findings revealed that higher sludge addition ratios significantly increased the activities of CBH, BG, NAG, and ALP enzymes, consistent with the insights of Pokharel et al. [47] into the impact of biochar on 12 soil enzyme activities. These results indicated that sludge incorporation substantially augmented soil enzymatic functions. Additionally, they confirmed that incubation temperature, sludge addition, and their combined effects critically influence soil enzyme dynamics.

4.2. Soil Nutrient and Enzyme Stoichiometry and Cumulative Carbon and Nitrogen Mineralization

Soil ecological stoichiometry provides critical insights into microbial activities and metabolic processes and serves as a diagnostic tool for evaluating resource limitations in soil nutrients [48,49]. In the present study, we observed that the soil enzyme C:P and N:P ratios exhibited marked increases with increasing temperatures, whereas the C:N ratio was significantly reduced. This aligns with the results of Bárta et al. [50], who analyzed stoichiometric ratios of enzymes involved in the cycling of carbon, nitrogen, and phosphorus in forest soils, revealing that increasing temperatures preferentially enhanced enzyme activities associated with carbon and nitrogen cycles over those linked to phosphorus cycles, with nitrogen-related enzyme activities surpassing those of carbon-related enzyme activities. Furthermore, our study established a robust correlation between soil and soil enzyme ecological stoichiometry ratios, corroborating the empirical evidence presented by Zhang et al. [51] and Yang et al. [52] regarding the stoichiometric ratios of soil carbon, nitrogen, and phosphorus. In addition, our findings demonstrated that the addition of sludge led to significant increases in soil C:P, N:P, enzyme C:P, and enzyme N:P ratios, which is consistent with the results of Geng et al. [11] and Chang et al. [53]. This suggests that sludge application notably augments SOC and TN levels, as well as enzymatic activities pertinent to the carbon and nitrogen cycles relative to those of phosphorus. Binh and Shima [54] reported that enhanced sludge application substantially increased soil nitrogen levels and decreased the soil C:N ratio, effectively moderating the net nitrogen mineralization rate and thereby regulating soil nitrogen mineralization processes. These results are consistent with our findings, which demonstrated notable reductions in the soil C:N and soil enzyme C:N ratios with increasing sludge addition, together with a significant decline in soil net nitrogen mineralization when sludge proportions exceeded 5.0%.
SOC and nitrogen mineralization primarily result from enzymatic reactions mediated by soil microorganisms, with elevated temperatures known to accelerate certain enzymatic activities. Consequently, numerous studies have demonstrated a positive correlation between the cumulative mineralization of SOC and nitrogen and ambient temperature [55,56]. Engqvist [57] revealed that increasing temperatures enhanced soil microbial biomass and enzyme activity, thereby accelerating the mineralization of organic carbon in the soil and subsequent CO2 production. They found that the microbial decomposition of organic matter predominantly governs the mineralization processes of SOC and nitrogen. Moreover, microbial respiration relies on extracellular enzymes to catalyze and hydrolyze organic matter, thereby acquiring the necessary carbon and nitrogen for metabolic functions. Weedon et al. [58] demonstrated that higher temperatures facilitate rapid soil nutrient decomposition with a robust microbial metabolism that secretes an abundance of soil enzymes, thus accelerating the mineralization of SOC and nitrogen. Wei et al. [59] demonstrated that augmenting soil with exogenous carbon increases the active carbon pool within the SOC. Enzyme kinetics theory suggests that soils deficient in organic carbon exhibit elevated activation energies. Consequently, in Wei et al. [59], with an increasing proportion of incorporated exogenous carbon, the soil mineralization rate decreased. In the present study, composted sludge treatments ranging from 10.0% to 20.0% failed to yield substantial net cumulative mineralization across various thermal conditions. As the application rate increased, a decrease in cumulative mineralization was observed, congruent with an enhancement in the capacity of the soil for carbon sequestration. Dais et al. [60] elucidated that biochar application beneficially affects SOC content, stabilizes the soil carbon pool, and bolsters soil carbon sequestration. They observed that biochar supplementation diminished the relative potential of soil mineralization and exerted a suppressive influence on the mineralization potential of SOC upon the addition of exogenous carbon. Furthermore, they ascertained that throughout the mineralization process, the cumulative mineralization of carbon and nitrogen in soil organic matter increased with increasing temperature. The principal rationale is that lower temperatures constrain the activity of soil microbes, thereby curtailing the production of active enzymes and impeding the progression of mineralization. Conversely, elevated temperatures enhance the activity of soil microbes, promoting the synthesis of enzymes involved in the mineralization of SOC and nitrogen. Increasing temperatures predominantly amplify the activity of soil microbes and enzymes, thereby extensively influencing the mineralization of SOC and nitrogen.

4.3. Factors Impacting the Variation of Soil Carbon and Nitrogen Mineralization

Net carbon and nitrogen mineralization in the soil have synergistic effects [61]. The present study established a significant linear correlation between the cumulative mineralization of net organic carbon and net nitrogen in the soil. This corroborates the findings of Wu et al. [62], who reported that fertilization modulates the mineralization of SOC and nitrogen reserves, which coincides with our Hypothesis (3). The mineralization rates of both carbon and nitrogen in the soil increase significantly with increasing temperature [63,64]. In the present study, across various incubation temperatures, the cumulative net carbon and nitrogen mineralization in the soil treated with sludge significantly exceeded that of CK. This suggests that elevated temperatures profoundly influence the availability and net mineralization of carbon and nitrogen in the soil. The cumulative mineralization of organic carbon and nitrogen in the soil is positively correlated with SOC concentration [65,66]. Sludge addition can enhance carbon sequestration and nutrient availability in the soil, although this effect is contingent on the proportion of sludge used. Our results revealed a significant linear relationship between the cumulative mineralization of net carbon and net nitrogen in the soil and the proportion of sludge used, although the cumulative mineralization levels were not statistically significant after applying 10.0% sludge. However, as the application rate increased, a downward trend in the cumulative mineralization of net nitrogen was observed, concurrent with an enhancement in the soil nutrient retention capacity. A random forest model indicated that temperature, NO3, BG, NAG, CBH, and ALP enzymes were critical determinants of net carbon and nitrogen mineralization in the soil. Correspondingly, various studies have identified temperature and soil enzyme activity as pivotal indicators that facilitate the net mineralization of carbon and nitrogen [67]. Using the SEM, we determined that the overall impacts of incubation temperature on net cumulative soil carbon and nitrogen mineralization surpassed those of sludge addition. This is consistent with the findings of Marzi et al. [61] on the influence of various sources of organic matter on soil carbon and nitrogen mineralization, while also supporting Hypothesis (2). Furthermore, this study identified NO3 as the primary factor affecting the cumulative mineralization of net soil carbon and nitrogen [68]. These results demonstrated that sludge addition and temperature influenced the net cumulative mineralization of carbon and nitrogen both directly and indirectly, mediated by soil chemical properties and enzymatic activity. Overall, this laboratory-based study evaluated the effects of temperature and sludge addition on the net mineralization of SOC and nitrogen and elucidated the principal interactions among soil chemical properties, enzyme activity, and ecological stoichiometry throughout the mineralization process.
In summary, we found that soil net carbon mineralization tended to be stable at a 5.0% to 10.0% sludge addition, whereas soil net nitrogen mineralization peaked. This sludge addition rate appears to be the most conducive to the remediation of degraded soils, as the soil carbon sequestration capacity is stable, while the soil mineralized inorganic nitrogen produces the maximum effective nitrogen that can be utilized by plants. Nevertheless, extensive research has confirmed the highly dynamic nature of soil carbon and nitrogen mineralization processes [69,70], showing that these are not only affected by the external environment but are also closely related to the internal nutrient changes in the soil. Therefore, additional field studies are required to assess the characteristics of SOC and nitrogen mineralization in response to temperature changes and the addition of sludge more accurately.

5. Conclusions

Our investigation uncovered substantial variations in soil chemical properties, enzyme activities, ecological stoichiometry, and cumulative net carbon and nitrogen mineralization under different temperatures and sludge addition rates. Elevated temperatures promoted soil DOC, NO3, and AP contents, together with soil CBH, BG, NAG, and ALP enzyme activities, thereby enhancing soil net carbon and nitrogen cumulative mineralization while significantly decreasing soil SOC and NH4+ contents and soil C:N. For its part, sludge addition increased the SOC, TN, TP, and NH4+ contents, soil CBH, BG, NAG, and ALP enzyme activities, soil enzyme C:P and enzyme N:P, and the net carbon and nitrogen cumulative mineralization capacity of the soil. The total effect of incubation temperature on soil C:N mineralization was greater than that of sludge addition, but NO3 was the main factor affecting soil C:N mineralization. Based on these results, we suggest that a sludge application rate of 5.0% to 10.0% can significantly improve the soil nutrient content. Simultaneously, the soil carbon sequestration capacity remains stable, while the effective nitrogen produced by soil inorganic nitrogen mineralization available to plants is maximized, which is the most conducive to the restoration of degraded soils. However, further studies are needed to understand the transformation mechanisms of incubation temperatures and soil NO3 in the soil carbon mineralization-fixation cycle more comprehensively.

Author Contributions

Writing—original draft preparation, methodology, data curation, X.M.; writing—review and editing, funding acquisition, resources, L.X.; writing—review and editing, methodology, resources, Z.L. and P.L.; writing—review and editing, software, formal analysis, F.W.; writing—review and editing, visualization, formal analysis, X.L.; writing—review and editing, investigation, validation, Z.W., S.C. and L.P. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Natural Science Foundation of China (42377350) and the key projects of the Shaanxi Provincial Department of Education (22JY043).

Data Availability Statement

The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Chen, J.; Chen, J.Z.; Tan, M.Z.; Gong, Z.T. Soil degradation: A global problem endangering sustainable development. J. Geogr. Sci. 2002, 12, 243–252. [Google Scholar]
  2. Ferreira, C.S.; Seifollahi, A.S.; Destouni, G.; Ghajarnia, N.; Kalantari, Z. Soil degradation in the European Mediterranean region: Processes, status and consequences. Sci. Total Environ. 2022, 805, 150106. [Google Scholar] [CrossRef]
  3. Ding, A.; Zhang, R.R.; Hao, N.H.; He, X.; Ma, J.; Nan, J.; Li, G.B. Life cycle assessment of sewage sludge treatment and disposal based on nutrient and energy recovery: A review. Sci. Total Environ. 2021, 769, 144451. [Google Scholar] [CrossRef]
  4. Xie, S.; Tran, H.; Pu, M.; Zhang, T. Transformation characteristics of organic matter and phosphorus in composting processes of agricultural organic waste: Research trends. Mater. Sci. Energy Technol. 2023, 6, 331–342. [Google Scholar] [CrossRef]
  5. Smith, P.; Fang, C.; Dawson, J.J.; Moncrieff, J.B. Impact of global warming on soil organic carbon. Adv. Agron. 2008, 97, 1–43. [Google Scholar]
  6. Fernandes, S.A.P.; Bettiol, W.; Cerri, C.C. Effect of sewage sludge on microbial biomass, basal respiration, metabolic quotient and soil enzymatic activity. Appl. Soil Ecol. 2005, 30, 65–77. [Google Scholar] [CrossRef]
  7. Paz-Ferreiro, J.; Gasco, G.; Gutiérrez, B.; Mendez, A. Soil biochemical activities and the geometric mean of enzyme activities after application of sewage sludge and sewage sludge biochar to soil. Biol. Fertil. Soils 2012, 48, 511–517. [Google Scholar] [CrossRef]
  8. Sastre, C.I.; Lobo, M.C.; Beltrán, H.R.I.; Poggi, V.H.M. Remediation of saline soils by a two-step process: Washing and amendment with sludge. Geoderma 2015, 247, 140–150. [Google Scholar] [CrossRef]
  9. Yue, Y.; Cui, L.; Lin, Q.M.; Li, G.T.; Zhao, X.R. Efficiency of sewage sludge biochar in improving urban soil properties and promoting grass growth. Chemosphere 2017, 173, 551–556. [Google Scholar] [CrossRef]
  10. Ahmad, A.; Chowdhary, P.; Khan, N.; Chaurasia, D.; Varjani, S.; Pandey, A.; Chaturvedi, P. Effect of sewage sludge biochar on the soil nutrient, microbial abundance, and plant biomass: A sustainable approach towards mitigation of solid waste. Chemosphere 2022, 287, 132112. [Google Scholar] [CrossRef]
  11. Geng, Z.; Xiao, L.; Li, Z.B.; Li, P.; Yao, K.H.; Chen, Y.X. Impacts of Adding Municipal Sewage Sludge on Soil Enzyme Activity and Stoichiometry in a Chinese Loess Soil. Pol. J. Environ. Stud. 2022, 31, 3031–3041. [Google Scholar] [CrossRef]
  12. Geng, Y.; Baumann, F.; Song, C.; Zhang, M.; Shi, Y.; Kühn, P.; Scholten, T.; He, J. Increasing temperature reduces the coupling between available nitrogen and phosphorus in soils of Chinese grasslands. Sci. Rep. 2017, 7, 43524. [Google Scholar] [CrossRef]
  13. Qi, R.M.; Li, J.; Lin, Z.; Li, Z.J.; Li, Y.T.; Yang, X.D.; Zhang, J.J.; Zhao, B.Q. Temperature effects on soil organic carbon, soil labile organic carbon fractions, and soil enzyme activities under long-term fertilization regimes. Appl. Soil Ecol. 2016, 102, 36–45. [Google Scholar] [CrossRef]
  14. Wallenstein, M.; Allison, S.D.; Ernakovich, J.; Steinweg, J.M.; Sinsabaugh, R. Controls on the temperature sensitivity of soil enzymes: A key driver of in situ enzyme activity rates. In Soil Enzymology; Springer: Berlin/Heidelberg, Germany, 2011; pp. 245–258. [Google Scholar]
  15. Wang, Q.K.; Zhao, X.C.; Chen, L.C.; Yang, Q.P.; Chen, S.; Zhang, W.D. Global synthesis of temperature sensitivity of soil organic carbon decomposition: Latitudinal patterns and mechanisms. Funct. Ecol. 2019, 33, 514–523. [Google Scholar] [CrossRef]
  16. Xiao, L.; Liu, G.B.; Li, P.; Xue, S. Ecological stoichiometry of plant-soil-enzyme interactions drives secondary plant succession in the abandoned grasslands of Loess Plateau, China. Catena 2021, 202, 105302. [Google Scholar] [CrossRef]
  17. Tan, Q.; Wang, G.; Smith, M.D.; Chen, Y.; Yu, Q. Temperature patterns of soil carbon: Nitrogen: Phosphorus stoichiometry along the 400 mm isohyet in China. Catena 2021, 203, 105338. [Google Scholar] [CrossRef]
  18. Pedra, F.; Polo, A.; Ribeiro, A.; Domingues, H. Effects of municipal solid waste compost and sewage sludge on mineralization of soil organic matter. Soil Biol. Biochem. 2007, 39, 1375–1382. [Google Scholar] [CrossRef]
  19. Davidson, E.A.; Janssens, I.A. Temperature sensitivity of soil carbon decomposition and feedbacks to climate change. Nature 2006, 440, 165–173. [Google Scholar] [CrossRef] [PubMed]
  20. Pérez, L.A.L.; Delgado, G.; Párraga, J.; Delgado, R.; Almendros, G.; Aranda, V. Evolution of organic matter fractions after application of co-compost of sewage sludge with pruning waste to four Mediterranean agricultural soils. A soil microcosm experiment. Waste Manag. 2010, 30, 1957–1965. [Google Scholar] [CrossRef] [PubMed]
  21. Zhang, X.; Zhao, Y.; Zhu, L.J.; Cui, H.Y.; Jia, L.M.; Xie, X.Y.; Li, J.M.; Wei, Z.M. Assessing the use of composts from multiple sources based on the characteristics of carbon mineralization in soil. Waste Manag. 2017, 70, 30–36. [Google Scholar] [CrossRef] [PubMed]
  22. Chen, L.J.; Jiang, Y.J.; Liang, C.; Luo, Y.; Xu, Q.S.; Han, C.; Zhao, Q.G.; Sun, B. Competitive interaction with keystone taxa induced negative priming under biochar amendments. Microbiome 2019, 7, 77. [Google Scholar] [CrossRef] [PubMed]
  23. Ribbons, R.R.; Levy, B.D.J.; Masse, J.; Grayston, S.J.; McDonald, M.A.; Vesterdal, L.; Prescott, C.E. Linking microbial communities, functional genes and nitrogen-cycling processes in forest floors under four tree species. Soil Biol. Biochem. 2016, 103, 181–191. [Google Scholar] [CrossRef]
  24. Zhang, J.B.; Cai, Z.C.; Müller, C. Terrestrial N cycling associated with climate and plant-specific N preferences: A review. Eur. J. Soil Sci. 2018, 69, 488–501. [Google Scholar] [CrossRef]
  25. Wang, X.; Yoo, K.; Wackett, A.A.; Gutknecht, J.; Amundson, R.; Heimsath, A. Soil organic carbon and mineral interactions on climatically different hillslopes. Geoderma 2018, 322, 71–80. [Google Scholar] [CrossRef]
  26. Zhou, S.; Li, P.; Zhang, Y.; Zhang, N.; Cao, Y. Formation of new erosion-deposition patterns after farmland conversion: The major role of topography. Catena 2023, 231, 107349. [Google Scholar] [CrossRef]
  27. Hu, H.; Umbreen, S.; Zhang, Y.; Bao, M.; Huang, C.; Zhou, C. Significant association between soil dissolved organic matter and soil microbial communities following vegetation restoration in the Loess Plateau. Ecol. Eng. 2021, 169, 106305. [Google Scholar] [CrossRef]
  28. Hall, P.J.; Aller, R.C. Rapid, small-volume, flow injection analysis for SCO2, and NH4+ in marine and freshwaters. Limnol. Oceanogr. 1992, 37, 1113–1119. [Google Scholar] [CrossRef]
  29. Saiya-Cork, K.R.; Sinsabaugh, R.L.; Zak, D.R. The effects of long term nitrogen deposition on extracellular enzyme activity in an Acer saccharum forest soil. Soil Biol. Biochem. 2002, 34, 1309–1315. [Google Scholar] [CrossRef]
  30. Xiao, L.; Liu, G.B.; Li, P.; Xue, S. Dynamics of soil specific enzyme activities and temperature sensitivities during grassland succession after farmland abandonment. Catena 2021, 199, 105081. [Google Scholar] [CrossRef]
  31. Kolisnik, T.; Keshavarz-Rahaghi, F.; Purcell, R.V.; Smith, A.N.; Silander, O.K. pyRforest: A comprehensive R package for genomic data analysis featuring scikit-learn Random Forests in R. bioRxiv 2024, 9, 598161. [Google Scholar]
  32. Oksanen, J.; Blanchet, F.G.; Kindt, R.; Legendre, P.; Minchin, P.R.; O’Hara, R.B.; Simpson, G.L.; Solymos, P.; Stevens, M.H.H.; Wagner, H. Community ecology package. R Package Version 2013, 2, 321–326. [Google Scholar]
  33. R Core Team. R: A Language and Environment for Statistical Computing; R Foundation for Statistical Computing: Vienna, Austria, 2013. [Google Scholar]
  34. Ayub, M.A.; Usman, M.; Faiz, T.; Umair, M.; Ul Haq, M.A.; Rizwan, M.; Ali, S.; Zia Ur Rehman, M. Restoration of degraded soil for sustainable agriculture. In Soil Health Restoration and Management; Springer: Berlin/Heidelberg, Germany, 2020; pp. 31–81. [Google Scholar]
  35. Hu, X.X.; Zhang, Y.X.; Wang, D.; Ma, J.; Xue, K.B.; An, Z.B.; Luo, W.X.; Sheng, Y.Z. Effects of temperature and humidity on soil gross nitrogen transformation in a typical shrub ecosystem in Yanshan Mountain and Hilly Region. Life 2023, 13, 643. [Google Scholar] [CrossRef] [PubMed]
  36. Song, Y.Y.; Song, C.C.; Hou, A.X.; Ren, J.S.; Wang, X.W.; Cui, Q.; Wang, M.Q. Effects of temperature and root additions on soil carbon and nitrogen mineralization in a predominantly permafrost peatland. Catena 2018, 165, 381–389. [Google Scholar] [CrossRef]
  37. Lehtinen, T.; Dersch, G.; Söllinger, J.; Baumgarten, A.; Schlatter, N.; Aichberger, K.; Spiegel, H. Long-term amendment of four different compost types on a loamy silt Cambisol: Impact on soil organic matter, nutrients and yields. Arch. Agron. Soil Sci. 2017, 63, 663–673. [Google Scholar] [CrossRef]
  38. Jakubus, M.; Bakinowska, E.; Gałka, B. The quantitative changes of nutrients in two contrasting soils amended with sewage sludge compost evaluated by various statistical tools. Acta Agric. Scand. Sect. B—Soil Plant Sci. 2018, 68, 39–49. [Google Scholar] [CrossRef]
  39. De Lucia, B.; Cristiano, G.; Vecchietti, L.; Bruno, L. Effect of different rates of composted organic amendment on urban soil properties, growth and nutrient status of three Mediterranean native hedge species. Urban For. Urban Green. 2013, 12, 537–545. [Google Scholar] [CrossRef]
  40. Elsalam, H.E.A.; El-Sharnouby, M.E.; Mohamed, A.E.; Raafat, B.M.; El-Gamal, E.H. Effect of sewage sludge compost usage on corn and faba bean growth, carbon and nitrogen forms in plants and soil. Agronomy 2021, 11, 628. [Google Scholar] [CrossRef]
  41. Jiang, J.; Xiong, Y.; Jiang, H.; De-You, Y.E.; Ya-Jie, S.; Feng-Min, L.I. Soil microbial activity during secondary vegetation succession in semiarid abandoned lands of Loess Plateau. Pedosphere 2009, 19, 735–747. [Google Scholar] [CrossRef]
  42. Ashraf, M.N.; Jusheng, G.; Lei, W.; Mustafa, A.; Waqas, A.; Aziz, T.; Khan, W.; Hussain, B.; Farooq, M.; Wenju, Z. Soil microbial biomass and extracellular enzyme–mediated mineralization potentials of carbon and nitrogen under long-term fertilization (> 30 years) in a rice–rice cropping system. J. Soils Sediments 2021, 21, 3789–3800. [Google Scholar] [CrossRef]
  43. Burke, D.J.; Weintraub, M.N.; Hewins, C.R.; Kalisz, S. Relationship between soil enzyme activities, nutrient cycling and soil fungal communities in a northern hardwood forest. Soil Biol. Biochem. 2011, 43, 795–803. [Google Scholar] [CrossRef]
  44. Meng, C.; Tian, D.S.; Zeng, H.; Li, Z.L.; Chen, H.Y.; Niu, S.L. Global meta-analysis on the responses of soil extracellular enzyme activities to warming. Sci. Total Environ. 2020, 705, 135992. [Google Scholar] [CrossRef] [PubMed]
  45. Steinweg, J.M.; Dukes, J.S.; Wallenstein, M.D. Modeling the effects of temperature and moisture on soil enzyme activity: Linking laboratory assays to continuous field data. Soil Biol. Biochem. 2012, 55, 85–92. [Google Scholar] [CrossRef]
  46. Skowrońska, M.; Bielińska, E.J.; Szymański, K.; Futa, B.; Antonkiewicz, J.; Kołodziej, B. An integrated assessment of the long-term impact of municipal sewage sludge on the chemical and biological properties of soil. Catena 2020, 189, 104484. [Google Scholar] [CrossRef]
  47. Pokharel, P.; Ma, Z.; Chang, S.X. Biochar increases soil microbial biomass with changes in extra-and intracellular enzyme activities: A global meta-analysis. Biochar 2020, 2, 65–79. [Google Scholar] [CrossRef]
  48. Luo, G.W.; Xue, C.; Jiang, Q.H.; Xiao, Y.; Zhang, F.G.; Guo, S.W.; Shen, Q.R.; Ling, N. Soil carbon, nitrogen, and phosphorus cycling microbial populations and their resistance to global change depend on soil C: N: P stoichiometry. Msystems 2020, 5, 10-1128. [Google Scholar] [CrossRef]
  49. Sinsabaugh, R.L.; Hill, B.H.; Follstad Shah, J.J. Ecoenzymatic stoichiometry of microbial organic nutrient acquisition in soil and sediment. Nature 2009, 462, 795–798. [Google Scholar] [CrossRef] [PubMed]
  50. Bárta, J.; Šlajsová, P.; Tahovská, K.; Picek, T.; Šantrůčková, H. Different temperature sensitivity and kinetics of soil enzymes indicate seasonal shifts in C, N and P nutrient stoichiometry in acid forest soil. Biogeochemistry 2014, 117, 525–537. [Google Scholar] [CrossRef]
  51. Zhang, W.; Liu, W.C.; Xu, M.P.; Deng, J.; Han, X.H.; Yang, G.H.; Feng, Y.Z.; Ren, G.X. Response of forest growth to C: N: P stoichiometry in plants and soils during Robinia pseudoacacia afforestation on the Loess Plateau, China. Geoderma 2019, 337, 280–289. [Google Scholar] [CrossRef]
  52. Yang, Y.; Liu, B.; An, S. Ecological stoichiometry in leaves, roots, litters and soil among different plant communities in a desertified region of Northern China. Catena 2018, 166, 328–338. [Google Scholar] [CrossRef]
  53. Chang, Y.B.; Liu, W.G.; Mao, Y.Q.; Yang, T.; Chen, Y.G. Biochar addition alters C: N: P stoichiometry in moss crust-soil continuum in Gurbantünggüt desert. Plants 2022, 11, 814. [Google Scholar] [CrossRef]
  54. Binh, N.T.; Shima, K. Nitrogen mineralization in soil amended with compost and urea as affected by plant residues supplements with controlled C/N ratios. J. Adv. Agric. Technol. 2018, 5, 8–13. [Google Scholar] [CrossRef]
  55. Leirós, M.C.; Trasar-Cepeda, C.; Seoane, S.; Gil-Sotres, F. Dependence of mineralization of soil organic matter on temperature and moisture. Soil Biol. Biochem. 1999, 31, 327–335. [Google Scholar] [CrossRef]
  56. Liu, Y.; Kumar, A.; Tiemann, L.K.; Li, J.; Chang, J.; Xu, L.; He, N. Substrate availability reconciles the contrasting temperature response of SOC mineralization in different soil profiles. J. Soils Sediments 2024, 24, 17–31. [Google Scholar] [CrossRef]
  57. Engqvist, M.K. Correlating enzyme annotations with a large set of microbial growth temperatures reveals metabolic adaptations to growth at diverse temperatures. BMC Microbiol. 2018, 18, 177. [Google Scholar] [CrossRef] [PubMed]
  58. Weedon, J.T.; Aerts, R.; Kowalchuk, G.A.; van Logtestijn, R.; Andringa, D.; van Bodegom, P.M. Temperature sensitivity of peatland C and N cycling: Does substrate supply play a role? Soil Biol. Biochem. 2013, 61, 109–120. [Google Scholar] [CrossRef]
  59. Wei, L.; Zhu, Z.K.; Liu, S.L.; Xiao, M.L.; Wang, J.Y.; Deng, Y.W.; Kuzyakov, Y.; Wu, J.S.; Ge, T.D. Temperature sensitivity (Q10) of stable, primed and easily available organic matter pools during decomposition in paddy soil. Appl. Soil Ecol. 2021, 157, 103752. [Google Scholar] [CrossRef]
  60. Dai, S.; Li, L.; Ye, R.; Zhu-Barker, X.; Horwath, W.R. The temperature sensitivity of organic carbon mineralization is affected by exogenous carbon inputs and soil organic carbon content. Eur. J. Soil Biol. 2017, 81, 69–75. [Google Scholar] [CrossRef]
  61. Marzi, M.; Shahbazi, K.; Kharazi, N.; Rezaei, M. The influence of organic amendment source on carbon and nitrogen mineralization in different soils. J. Soil Sci. Plant Nutr. 2020, 20, 177–191. [Google Scholar] [CrossRef]
  62. Wu, H.L.; Cai, A.D.; Xing, T.T.; Huai, S.C.; Zhu, P.; Xu, M.G.; Lu, C.G. Fertilization enhances mineralization of soil carbon and nitrogen pools by regulating the bacterial community and biomass. J. Soils Sediments 2021, 21, 1633–1643. [Google Scholar] [CrossRef]
  63. Donhauser, J.; Qi, W.; Bergk Pinto, B.; Frey, B. High temperatures enhance the microbial genetic potential to recycle C and N from necromass in high-mountain soils. Glob. Chang. Biol. 2021, 27, 1365–1386. [Google Scholar] [CrossRef]
  64. Liu, Y.; Wang, C.H.; He, N.P.; Wen, X.F.; Gao, Y.; Li, S.G.; Niu, S.L.; Butterbach Bahl, K.; Luo, Y.Q.; Yu, G.R. A global synthesis of the rate and temperature sensitivity of soil nitrogen mineralization: Latitudinal patterns and mechanisms. Glob. Chang. Biol. 2017, 23, 455–464. [Google Scholar] [CrossRef]
  65. Guo, Z.; Han, J.; Li, J.; Xu, Y.; Wang, X. Effects of long-term fertilization on soil organic carbon mineralization and microbial community structure. PLoS ONE 2019, 14, e0211163. [Google Scholar]
  66. Weintraub, M.N.; Schimel, J.P. Interactions between carbon and nitrogen mineralization and soil organic matter chemistry in arctic tundra soils. Ecosystems 2003, 6, 129–143. [Google Scholar] [CrossRef]
  67. Tabatabai, M.A.; Ekenler, M.; Senwo, Z.N. Significance of enzyme activities in soil nitrogen mineralization. Commun. Soil Sci. Plant Anal. 2010, 41, 595–605. [Google Scholar] [CrossRef]
  68. Ali, S.; Liu, K.; Ahmed, W.; Jing, H.; Qaswar, M.; Kofi Anthonio, C.; Maitlo, A.A.; Lu, Z.; Liu, L.; Zhang, H. Nitrogen mineralization, soil microbial biomass and extracellular enzyme activities regulated by long-term N fertilizer inputs: A comparison study from upland and paddy soils in a red soil region of China. Agronomy 2021, 11, 2057. [Google Scholar] [CrossRef]
  69. Chen, Q.; Hu, Y.; Hu, A.; Niu, B.; Yang, X.; Jiao, H.; Song, L.; Zhang, G. Shifts in the dynamic mechanisms of soil organic matter transformation with nitrogen addition: From a soil carbon/nitrogen-driven mechanism to a microbe-driven mechanism. Soil Biol. Biochem. 2021, 160, 108355. [Google Scholar] [CrossRef]
  70. Salinas, G.J.R.; Hons, F.M.; Matocha, J.E.; Zuberer, D.A. Soil carbon and nitrogen dynamics as affected by long-term tillage and nitrogen fertilization. Biol. Fertil. Soils 1997, 25, 182–188. [Google Scholar] [CrossRef]
Figure 1. Effect of incubation temperature and sludge addition on soil nutrient properties. Note: Different uppercase letters indicate significant differences among sludge addition treatments at the same incubation temperatures (p < 0.05). Different lowercase letters indicate significant differences among different incubation temperatures at the same sludge addition treatment (p < 0.05). T: incubation temperature, SA: sludge addition, T&SA: interactive effect of incubation temperature and sludge addition. Statistical significance is indicated as follows: *, p < 0.05; **, p < 0.01; ***, p < 0.001. The same as below.
Figure 1. Effect of incubation temperature and sludge addition on soil nutrient properties. Note: Different uppercase letters indicate significant differences among sludge addition treatments at the same incubation temperatures (p < 0.05). Different lowercase letters indicate significant differences among different incubation temperatures at the same sludge addition treatment (p < 0.05). T: incubation temperature, SA: sludge addition, T&SA: interactive effect of incubation temperature and sludge addition. Statistical significance is indicated as follows: *, p < 0.05; **, p < 0.01; ***, p < 0.001. The same as below.
Agronomy 14 01590 g001aAgronomy 14 01590 g001b
Figure 2. Effect of incubation temperature and sludge addition on soil enzyme activities. Note: Different uppercase letters indicate significant differences among sludge addition treatments at the same incubation temperatures (p < 0.05). Different lowercase letters indicate significant differences among different incubation temperatures at the same sludge addition treatment (p < 0.05). T: incubation temperature, SA: sludge addition, T&SA: interactive effect of incubation tem-perature and sludge addition. Statistical significance is indicated as follows: ***, p < 0.001.
Figure 2. Effect of incubation temperature and sludge addition on soil enzyme activities. Note: Different uppercase letters indicate significant differences among sludge addition treatments at the same incubation temperatures (p < 0.05). Different lowercase letters indicate significant differences among different incubation temperatures at the same sludge addition treatment (p < 0.05). T: incubation temperature, SA: sludge addition, T&SA: interactive effect of incubation tem-perature and sludge addition. Statistical significance is indicated as follows: ***, p < 0.001.
Agronomy 14 01590 g002
Figure 3. Effect of incubation temperature and sludge addition on the ecological stoichiometry ratios of soil nutrients and soil enzyme activities. Note: Different uppercase letters indicate significant differences among sludge addition treatments at the same incubation temperatures (p < 0.05). Different lowercase letters indicate significant differences among different incubation temperatures at the same sludge addition treatment (p < 0.05). T: Incubation incubation temperature, SA: Sludge sludge addition, T&SA: Interactive interactive effect of incubation temperature and sludge addition. Statistical significance is indicated as follows: ***, p < 0.001.
Figure 3. Effect of incubation temperature and sludge addition on the ecological stoichiometry ratios of soil nutrients and soil enzyme activities. Note: Different uppercase letters indicate significant differences among sludge addition treatments at the same incubation temperatures (p < 0.05). Different lowercase letters indicate significant differences among different incubation temperatures at the same sludge addition treatment (p < 0.05). T: Incubation incubation temperature, SA: Sludge sludge addition, T&SA: Interactive interactive effect of incubation temperature and sludge addition. Statistical significance is indicated as follows: ***, p < 0.001.
Agronomy 14 01590 g003aAgronomy 14 01590 g003b
Figure 4. Effect of incubation temperature and sludge addition on the cumulative mineralization of net soil organic carbon and nitrogen. Note: Different uppercase letters indicate significant differences among sludge addition treatments at the same incubation temperatures (p < 0.05). Different lowercase letters indicate significant differences among different incubation temperatures at the same sludge addition treatment (p < 0.05). T: Incubation incubation temperature, SA: Sludge sludge addition, T&SA: Interactive interactive effect of incubation temperature and sludge addition. Statistical significance is indicated as follows: ***, p < 0.001.
Figure 4. Effect of incubation temperature and sludge addition on the cumulative mineralization of net soil organic carbon and nitrogen. Note: Different uppercase letters indicate significant differences among sludge addition treatments at the same incubation temperatures (p < 0.05). Different lowercase letters indicate significant differences among different incubation temperatures at the same sludge addition treatment (p < 0.05). T: Incubation incubation temperature, SA: Sludge sludge addition, T&SA: Interactive interactive effect of incubation temperature and sludge addition. Statistical significance is indicated as follows: ***, p < 0.001.
Agronomy 14 01590 g004
Figure 5. Correlation between cumulative net soil organic carbon mineralization and cumulative net nitrogen mineralization.
Figure 5. Correlation between cumulative net soil organic carbon mineralization and cumulative net nitrogen mineralization.
Agronomy 14 01590 g005
Figure 6. Principal component analysis of soil chemical properties, soil enzyme activities, and their ecological stoichiometry, and net soil organic carbon and nitrogen cumulative mineralization under different incubation temperatures and sludge additions.
Figure 6. Principal component analysis of soil chemical properties, soil enzyme activities, and their ecological stoichiometry, and net soil organic carbon and nitrogen cumulative mineralization under different incubation temperatures and sludge additions.
Agronomy 14 01590 g006
Figure 7. Correlation analysis of soil chemical properties, soil enzymes, and their ecological stoichiometry, and cumulative net soil organic carbon and nitrogen mineralization. significance is indicated as follows: *, p < 0.05; **, p < 0.01; ***, p < 0.001.
Figure 7. Correlation analysis of soil chemical properties, soil enzymes, and their ecological stoichiometry, and cumulative net soil organic carbon and nitrogen mineralization. significance is indicated as follows: *, p < 0.05; **, p < 0.01; ***, p < 0.001.
Agronomy 14 01590 g007
Figure 8. Random forest model elucidating the influence of soil chemical properties, enzyme activities, and their ecological stoichiometry on net soil organic carbon and nitrogen mineralization across different incubation temperatures and sludge additions. (a) Significance of predictor variables for net cumulative soil organic carbon mineralization. (b) Significance of predictor variables for cumulative net nitrogen mineralization. Level of significance denoted as *, p < 0.05 and **, p < 0.01.
Figure 8. Random forest model elucidating the influence of soil chemical properties, enzyme activities, and their ecological stoichiometry on net soil organic carbon and nitrogen mineralization across different incubation temperatures and sludge additions. (a) Significance of predictor variables for net cumulative soil organic carbon mineralization. (b) Significance of predictor variables for cumulative net nitrogen mineralization. Level of significance denoted as *, p < 0.05 and **, p < 0.01.
Agronomy 14 01590 g008
Figure 9. Structural equation modeling delineating the direct and indirect impacts of incubation temperature and sludge addition on soil chemical properties, enzymatic activities, and the cumulative mineralization of soil organic carbon and nitrogen. Within the model, sludge addition is represented by a blue rectangle, and incubation temperature by a red rectangle. Positive and negative influences are encoded by blue and red lines, respectively. The breadth of the arrows quantifies the magnitude of significant standardized path coefficients, with non-significant pathways depicted in gray. TN: total nitrogen, AP: effective phosphorus, DOC: soluble organic carbon, NO3: nitrate nitrogen, CBH: cellobiohydrolase, BG: β-1,4-Glucosidase, ALP: alkaline phosphatase. Statistical significance is indicated as follows: *, p < 0.05; **, p < 0.01; ***, p < 0.001.
Figure 9. Structural equation modeling delineating the direct and indirect impacts of incubation temperature and sludge addition on soil chemical properties, enzymatic activities, and the cumulative mineralization of soil organic carbon and nitrogen. Within the model, sludge addition is represented by a blue rectangle, and incubation temperature by a red rectangle. Positive and negative influences are encoded by blue and red lines, respectively. The breadth of the arrows quantifies the magnitude of significant standardized path coefficients, with non-significant pathways depicted in gray. TN: total nitrogen, AP: effective phosphorus, DOC: soluble organic carbon, NO3: nitrate nitrogen, CBH: cellobiohydrolase, BG: β-1,4-Glucosidase, ALP: alkaline phosphatase. Statistical significance is indicated as follows: *, p < 0.05; **, p < 0.01; ***, p < 0.001.
Agronomy 14 01590 g009
Table 1. Basic chemical properties of grassland soil and sludge.
Table 1. Basic chemical properties of grassland soil and sludge.
TreatmentSOC
(g·kg−1)
TN
(g·kg−1)
TP
(g·kg−1)
DOC
(mg·kg−1)
NH4+
(mg·kg−1)
NO3
(mg·kg−1)
AP
(mg·kg−1)
Composted sludge237.54 ± 15.7022.23 ± 1.5417.10 ± 0.324391.11 ± 331.071154.33 ± 54.85199.68 ± 7.031070.40 ± 162.24
Grassland soil4.89 ± 0.120.38 ± 0.020.49 ± 0.0458.97 ± 5.2017.65 ± 1.9318.36 ± 4.3810.41 ± 1.62
Note: SOC: soil organic carbon; TN: soil total nitrogen; TP: soil total phosphorus; DOC: dissolved organic carbon; NH4+: ammonium nitrogen; NO3: nitrate nitrogen; AP: available phosphorus.
Table 2. Different soil enzyme functions and required substrates.
Table 2. Different soil enzyme functions and required substrates.
EnzymeAbbreviationSubstrateFunction
CellobiohydrolaseCBH4-MUB-N-acetyl-β-D-glucosaminideReleases disaccharides from cellulose
β-1,4-GlucosidaseBG4-MUB-β-D-glucosideReleases glucose from cellulose
β-1,4-N-acetyglucosaminidaseNAG4-MUB-β-D-cellobiosideReleases N-acetyl glucosamine from oligosaccharides
Alkaline PhosphataseALP4- MUB-phosphateHydrolysis of organophosphates to phosphates
Table 3. Direct, indirect, and total effects of sludge addition, incubation temperature, soil chemical properties, and soil enzyme activities on net cumulative soil carbon mineralization.
Table 3. Direct, indirect, and total effects of sludge addition, incubation temperature, soil chemical properties, and soil enzyme activities on net cumulative soil carbon mineralization.
Sludge AdditionIncubation TemperatureDOCNO3CBHBGNAGALPEnzymeC:P
Direct0.249-−0.1050.516-−0.4220.3580.2700.407
Indirect0.0620.666−0.0360.252−0.0770.377-−0.204-
Total0.3110.666−0.1410.768−0.077−0.0450.3580.0660.407
Table 4. Direct, indirect, and total effects of sludge addition, incubation temperature, soil chemical properties, and soil enzyme activities on cumulative mineralization of net soil nitrogen.
Table 4. Direct, indirect, and total effects of sludge addition, incubation temperature, soil chemical properties, and soil enzyme activities on cumulative mineralization of net soil nitrogen.
Sludge AdditionIncubation TemperatureNO3APCBHBGALPEnzymeC:P
Direct-0.1960.9700.019--0.1060.319
Indirect0.2290.683-−0.006−0.0590.302−0.158-
Total0.2290.8790.9700.013−0.0590.302−0.0520.319
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Min, X.; Xiao, L.; Li, Z.; Li, P.; Wang, F.; Liu, X.; Chen, S.; Wang, Z.; Pan, L. Effects of Incubation Temperature and Sludge Addition on Soil Organic Carbon and Nitrogen Mineralization Characteristics in Degraded Grassland Soil. Agronomy 2024, 14, 1590. https://doi.org/10.3390/agronomy14071590

AMA Style

Min X, Xiao L, Li Z, Li P, Wang F, Liu X, Chen S, Wang Z, Pan L. Effects of Incubation Temperature and Sludge Addition on Soil Organic Carbon and Nitrogen Mineralization Characteristics in Degraded Grassland Soil. Agronomy. 2024; 14(7):1590. https://doi.org/10.3390/agronomy14071590

Chicago/Turabian Style

Min, Xuxu, Lie Xiao, Zhanbin Li, Peng Li, Feichao Wang, Xiaohuang Liu, Shuyi Chen, Zhou Wang, and Lei Pan. 2024. "Effects of Incubation Temperature and Sludge Addition on Soil Organic Carbon and Nitrogen Mineralization Characteristics in Degraded Grassland Soil" Agronomy 14, no. 7: 1590. https://doi.org/10.3390/agronomy14071590

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Article metric data becomes available approximately 24 hours after publication online.
Back to TopTop