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Article

The Effects of Conservation Tillage on Chemical and Microbial Soil Parameters at Four Sites across Europe

1
Centre of Biodiversity and Sustainable Land Use, Georg August-University Goettingen, Büsgenweg 1, 37077 Goettingen, Germany
2
Department of Environmental and Plant Protection Engineering and Environmental Protection, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, 3-5 Calea Manastur Street, 400372 Cluj-Napoca, Romania
3
Soil Biology and Plant Nutrition, University of Kassel, Nordbahnhofstraße 1a, 7213 Witzenhausen, Germany
4
Department of Crop Sciences, Georg-August-University Goettingen, Von-Siebold-Straße 8, 37075 Goettingen, Germany
*
Authors to whom correspondence should be addressed.
Plants 2022, 11(13), 1747; https://doi.org/10.3390/plants11131747
Submission received: 30 May 2022 / Revised: 27 June 2022 / Accepted: 28 June 2022 / Published: 30 June 2022
(This article belongs to the Special Issue Conservation Tillage for Sustainable Agriculture)

Abstract

:
Conservation tillage is often discussed as an effective tool to improve the soil quality in agriculture. Four sites across Europe (in Germany, Romania, Spain, and Sweden) were investigated as case studies for country-specific reductions in tillage intensity. Conventional tillage (CT) by mouldboard ploughing was compared with shallow and deep non-inversion minimum tillage (MT) and/or no-tillage (NT). In Sweden, NT and MT had positive effects on the concentrations of soil organic carbon (SOC), total nitrogen (N), and microbial biomass carbon (MBC) in the upper 20 cm compared with CT. At the German site, MT increased SOC, N, and MBC concentrations in the top 10 cm. In contrast, CT increased MBC contents and bulk density between 20 and 30 cm soil depth. At the Romanian site, soil parameters showed no differences between inverse tillage (CT) and non-inverse tillage (MT), both with a working depth of 25 to 30 cm. At the Spanish site, the use of NT significantly increased the concentrations as well as the stocks of C, N, and MBC compared to CT. In conclusion, reduced tillage improved soil microbial properties in most cases. However, the effectiveness of reduced tillage appears to be highly dependent on site conditions such as pH, soil texture, and climatic conditions.

1. Introduction

Conservation tillage has the potential to promote soil organisms [1], enhance the water infiltration capacity of soils, and reduce the risk of water erosion [2,3]. Further, the potential for carbon (C) sequestration is also a strong motivation for reducing tillage intensity in order to mitigate climate change [4,5]. Techniques of conservation tillage generally increase C and nitrogen (N) contents in the soil surface layer, thereby improving the soil structure and accelerating the soil’s resilience to extreme weather conditions [6]. In addition, tillage systems with a mulch layer reduce the risk of wind erosion [7,8] and lessen evaporation processes [9]. Nevertheless, conventional tillage (CT) is still a common tillage system in most European countries [10,11,12]. Main arguments against no-tillage (NT) systems are yield loss due to weed competition [13] and problems with seed germination [14].
The effectiveness of conservation tillage to improve soil conditions is still difficult to predict as there are significant differences among the various techniques grouped under this term. For instance, NT can mean direct seeding without any tillage operations [15,16] or opening a narrow trench for sowing [17]. Minimum tillage (MT) can be applied with various machinery (e.g., a disc harrow or a rotary harrow) at 5 cm [18], down to 8 cm [19], between 10 and 15 cm [20,21] or even down to 20 cm [22]. In contrast, CT is defined more uniformly in Europe, using a mouldboard plough at a working depth of between 20 and 30 cm [10,15,23].
In order to assess the advantages of conservation tillage over ploughing, indicators that reflect the status of soils are needed. Soil microbial properties as well as physicochemical soil characteristics are the two most important factors for the stability of a soil system [24]. To promote sustainable soil management and to improve soil fertility, an increase in surface-near nutrients and microbial biomass is recommended. The measurement of microbial biomass carbon (MBC) is a common tool to investigate the relationship between plant input, soil organic C (SOC) storage, nutrient mobilization and immobilisation processes [25,26]. MBC is often used in combination with measuring basal respiration, the mineralisation of SOC in the absence of fresh plant substrates [27,28]. In addition, the metabolic quotient qCO2 calculated as respiration-to-biomass ratio reflects the microbial demand for maintenance energy [29], whereas the ratio of MBC to SOC expresses the C availability for microorganisms [30]. Previous studies showed that conservation tillage, compared with ploughing, has the potential to increase MBC stocks and enhance microbial indicators [31,32,33,34]. In contrast, only moderate or even no increases in SOC stocks were found for non-inversion tillage treatments compared with mouldboard ploughing [21,35,36,37,38]. However, the effects seem to vary between sites and tillage regimes.
Agricultural soils are influenced by the long-term history of cultivation practices and current management decisions of the farmer. Therefore, the present study follows a regional approach and investigates four sites, where tillage intensity was reduced in a country-specific way to match the demand of local management. The effects of conservation tillage systems on microbial, chemical, and physical soil parameters are compared with those of ploughing. The aim of this study was to find out which tillage system improves soil properties and thus enhances soil quality the most, taking into account site-specific conditions. The four sites form a climate gradient from Northern Europe (Sweden), via Central Europe (Germany) to South-Eastern Europe (Romania) and South-Western Europe (Spain), representing large areas of arable land in each country. The following four hypotheses were examined: (1) The positive effects of reducing tillage intensity on MBC are most visible in the upper soil and decrease with soil depth. (2) SOC stocks are not significantly different between conventional mouldboard ploughing and conservation tillage when regarding the whole sampled soil profile, whereas (3) MBC stocks are increased by a tillage reduction. (4) However, the effectiveness of conservation tillage regarding MBC dynamics depends on site-specific conditions such as soil texture, pH, and climatic conditions.

2. Results and Discussion

2.1. Säby, Sweden

In Sweden, SOC contents varied around 25.9 mg g−1 soil and declined by 34% from the top to the bottom layer under MT and by 50% under NT. In contrast, SOC concentrations at 0–20 cm under CT were nearly equally distributed with highest amounts in the deepest soil layer. At 20–30 cm, SOC contents were significantly affected by tillage treatments (F = 16.99; p < 0.05); contents of SOC were significantly higher (p < 0.05) at CT than at NT or MT plots (Table 1 and Table 2). Total N contents were in a range from 1.6 to 2.7 mg g−1 soil and were significantly influenced by tillage (F = 7.60; p < 0.05) at 10–20 cm. Soil samples at 10–20 cm soil depth from CT plots had greater total N contents (p = 0.05) than those from NT (Table 2). MBC contents were in a range from 61 to 333 µg g−1 and differed significantly (F = 52.77; p < 0.01) between tillage treatments at 0–10 cm soil depth; MT (p < 0.01) and NT (p < 0.01) enhanced MBC contents strongly compared with CT (Figure 1).
Summing up, the 11 years of MT and NT increased the contents of SOC, total N, and MBC in the top layers, accompanied by a strong depth decline in the bottom 20–30 cm layer. Similar depth declines have been repeatedly observed in Sweden [31,39]. The increase at 0–10 cm and the depth decline were most pronounced for MBC, indicating a closer relationship to the actual C input than SOC and N already stored in soil [1,40]. This effect was intensified by the strong bulk density (BD) increase from the 0–10 cm to the 10–20 cm layer. This increase occurred under all three tillage systems but especially under MT and NT (+40%) vs. CT (+30%).
The BD varied around 1.02 g cm−3 at 0–10 cm and around 1.38 g cm−3 at 10–30 cm, without tillage effects at any depth (Table 2). The increased BD below followed from cultivation might form a barrier, which can reduce the C input by crop roots and, thus, MBC in the long-term [39,41,42]. The soil at this site, an acidic Eutric Cambisol, was characterised by high SOC stocks and low MBC stocks. Differences in SOC stocks were relatively strong between tillage treatments (F = 5.51; p = 0.07) whereas MBC stocks showed quite smaller variations (Table 3). The MBC/SOC ratio was around 0.7% among tillage treatments, which is most common in strongly acidic forest soils [29,43] and has rarely been measured in arable Cambisols [44], especially not in those with a relatively high clay content [25]. Acidification usually also increases the microbial demand for maintenance energy [29,45], which was reflected by high qCO2 values with a mean of 134 mg CO2-C g−1 MBC d−1 (0–30 cm soil depth). A high demand for maintenance energy lowers the MBC contents of a soil in the long-term [27,28]. However, low mean annual temperatures (MAT) and high mean annual precipitation (MAP) might also have reduced microbial decomposition of the annual C input, as indicated by the high SOC/total N ratio of 11.9. Overall, the study site at Säby is characterised by acidic conditions and low annual temperatures, high SOC contents and stocks. The low microbial availability of resources was reflected by low MBC/SOC ratios and quite small effects of tillage reduction on MBC contents.
Table 1. Overview of the different tillage treatments at the four field sites; CT = conventional tillage, MT = minimum tillage, NT = no-tillage.
Table 1. Overview of the different tillage treatments at the four field sites; CT = conventional tillage, MT = minimum tillage, NT = no-tillage.
SiteTillageMachinery Used (Working Depth)
SäbyCTMouldboard plough (23 cm)
MTCultivator (10–12 cm)
NTDirect seeding without any tillage operations
Garte SüdCTMouldboard plough (25–30 cm), followed by a rotary harrow
MTRotary harrow (5–8 cm)
TurdaCTMouldboard plough (25–30 cm), seedbed preparation by a rotary harrow
MTChisel processing (25–30 cm) after maize and wheat followed by disk harrow while direct seeding was applied after soybean
La HampaCTMouldboard plough (25–30 cm) plus cultivator (15–20 cm) and a disc harrow (15 cm)
NTDirect seeding without any tillage operations
Table 2. Mean (standard deviation) of bulk density, soil organic carbon (SOC) and total nitrogen (N) contents at the field sites Säby (n = 3), Garte Süd (n = 4), Turda (n = 3), and La Hampa (n = 3) under different tillage treatments (CT = conventional tillage, MT = minimum tillage, NT = no-tillage) at three soil depths (0–10 cm, 10–20 cm, 20–30 cm).
Table 2. Mean (standard deviation) of bulk density, soil organic carbon (SOC) and total nitrogen (N) contents at the field sites Säby (n = 3), Garte Süd (n = 4), Turda (n = 3), and La Hampa (n = 3) under different tillage treatments (CT = conventional tillage, MT = minimum tillage, NT = no-tillage) at three soil depths (0–10 cm, 10–20 cm, 20–30 cm).
SiteSoil DepthBulk Density (g cm−3)SOC (mg g−1 Soil)Total N (mg g−1 Soil)
(cm)CTMTNTCTMTNTCTMTNT
Säby 0–100.97 (0.10)1.01 (0.14)1.08 (0.16)26.67 (1.51)30.63 (1.55)34.90 (4.19)2.33 (0.05)2.53 (0.09)2.73 (0.19)
10–201.25 (0.11)1.41 (0.12)1.50 (0.07)27.00 (1.61)26.13 (2.76)23.53 (1.27)2.30 (0.08) a2.17 (0.12) ab1.97 (0.05) b
20–301.33 (0.18)1.43 (0.07)1.38 (0.13)26.73 (2.40) a20.17 (3.84) b17.67 (3.73) b2.20 (0.14)1.77 (0.17)1.63 (0.21)
Garte Süd 0–101.67 (0.12)1.66 (0.10) 14.38 (1.48) b18.28 (0.75) a 1.43 (0.04) b1.75 (0.05) a
10–201.63 (0.05)1.67 (0.09) 14.60 (0.99)14.80 (0.94) 1.50 (0.00)1.48 (0.04)
20–301.65 (0.05) b1.83 (0.03) a 14.60 (2.42)13.13 (1.61) 1.40 (0.07)1.30 (0.00)
Turda 0–100.89 (0.00)0.85 (0.01) 22.13 (0.39)20.67 (0.60) 2.13 (0.10)2.00 (0.00)
10–200.98 (0.02)0.88 (0.02) 22.53 (0.09)20.87 (1.53) 2.13 (0.10)2.00 (0.10)
20–301.01 (0.04)0.90 (0.03) 22.43 (0.33)19.53 (0.90) 2.13 (0.10)1.90 (0.00)
La Hampa 0–101.18 (0.29) 1.46 (0.19)9.03 (0.48) b 10.30 (0.62) a1.07 (0.05) 1.20 (0.08)
10–201.29 (0.25) 1.26 (0.03)8.23 (0.54) 9.13 (0.38)0.90 (0.08) 1.07 (0.05)
20–301.38 (0.05) 1.27 (0.16)7.77 (0.05) 7.90 (0.65)0.97 (0.05) 1.00 (0.08)
Different letters (a, b, ab) indicate a depth and site-specific significant difference between the tillage treatments (p < 0.05).
Table 3. Mean stocks (standard deviation) of soil organic carbon (SOC) and microbial biomass carbon (MBC) at the four field sites under different tillage treatments; CT = conventional tillage, MT = minimum tillage, NT = no-tillage. Information of tillage techniques are given in Table 1.
Table 3. Mean stocks (standard deviation) of soil organic carbon (SOC) and microbial biomass carbon (MBC) at the four field sites under different tillage treatments; CT = conventional tillage, MT = minimum tillage, NT = no-tillage. Information of tillage techniques are given in Table 1.
SiteEquivalent Soil MassSOC (t ha−1)MBC (t ha−1)
(t ha−1
0–30 cm)
CTMTNTCTMTNT
Säby (n = 3) 3790108.2 (1.5)86.7 (7.4)76.5 (13.7)0.72 (0.09)0.66 (0.04)0.68 (0.12)
Garte Süd (n =4) 506075.3 (9.7)76.2 (5.6) 1.62 (0.09)1.53 (0.13)
Turda (n = 3) 276059.0 (1.4)58.8 (2.0) 0.83 (0.05)0.77 (0.04)
La Hampa (n = 3) 379032.5 (1.1) b 36.0 (1.1) a0.78 (0.07) b 1.04 (0.02) a
Different letters (a, b) indicate a depth and site-specific significant difference between the tillage treatments (p < 0.05).

2.2. Garte Süd, Germany

Garte Süd is a long-lasting tillage experiment where the comparison between CT and MT already started 47 years ago [46]. Contents of SOC varied around 15.0 mg g−1 and the SOC/total N ratio was about 10 at Garte Süd. At 0–10 cm SOC contents were significantly (F = 36.07; p < 0.01) greater under MT compared with CT (Table 2). At the same soil depth, also total N contents were significantly greater (F = 169.00; p < 0.001) at MT plots than at CT plots (Table 1 and Table 2). MBC contents varied from 176 to 488 µg g−1 soil. In contrast to MT, the application of a mouldboard plough (CT) resulted in a homogenous distribution of SOC, total N and MBC concentrations in the sampled soil profile, presumably due to the strong mixing effect of this tool. At 0–10 cm soil depth, MBC contents were significantly (F = 14.50; p < 0.05) higher at MT compared with CT (Figure 1). Similar results have been repeatedly observed in Germany [32,37,41].
The soil at this site, a Haplic Luvisol, was characterised by high BD (mean of 1.69 g cm−3). At 20–30 cm soil depth BD was significantly (F = 31.23; p < 0.05) higher at MT compared with CT. The generally high BD is most likely caused by heavy machinery, especially for sugar beet harvesting in wet autumns [47]. Load-induced compaction is most likely the reason for the extremely high BD at 20–30 cm under MT. Generally, field crops have less difficulty with homogeneously high BD levels than with escalating increases [48]. This is in line with the study of Murugan et al. [32], who did not observe any yield difference between CT and MT at four sites in Germany for winter wheat and sugar beet.
This high BD led to the maximum equivalent soil mass, which is partly reflected by the SOC and MBC stocks. SOC and MBC stocks showed no differences between tillage practices (Table 3). In contrast, Heinze et al. [19] and Murugan et al. [32] observed approximately 10% higher SOC stocks and 20% higher MBC stocks on Luvisols in central Germany under MT in comparison with CT. However, these differences might be partly explained by a different sampling and calculation procedure [32]. The mean MBC/SOC ratio was 2.1% at Garte Süd, which is typical for central European Luvisols [19,32,37]. The mean metabolic quotient qCO2 value was on average 98 without significant differences between tillage practices. In conclusion, the field site Garte Süd is shaped by relatively high BD levels. The contents of SOC, total N and MBC differed in terms of tillage practices in the upper soil depth (0–10 cm), whereas stocks were not affected.

2.3. Turda, Romania

Turda was the only site, where MT and CT were carried out on a similar working depth. The soil, a Phaeozem, was characterised by a high clay content (>50%) and a low BD level with a mean of 0.92 g cm−3. MBC contents (0–30 cm depth) varied around 290 µg g−1 soil (Figure 1). SOC contents were on average 21.4 mg g−1 soil at Turda with a mean SOC/total N ratio of 10 (Table 1 and Table 2). Among tillage treatments, total N contents ranged from 19 to 22 mg g−1 soil in the upper 30 cm. Phaeozems, typical for Romanian cropland, are known for their high natural fertility [49]. The clay content at Turda was considerably above that of other European Phaeozems [50,51], which led to generally low BD values and might improve its resilience against tillage-induced compaction [52,53].
The changes of MBC contents with depth were moderate for both tillage techniques (Figure 1). The MBC decline at 20–30 cm under CT indicates that the mouldboard plough did not always reach a working depth of 30 cm. In accordance with current results, no differences in SOC contents with depth between mouldboard ploughing and deep non-inversion chisel tillage have been measured on a Mollisol in Ohio, USA [54]. In contrast, much higher SOC contents have been observed in the top layers of a deep non-inversion tillage treatment than in a mouldboard ploughing treatment on a typical Ukrainian Chernozem [51]. This discrepancy cannot be explained by the current study. Other experiments did not find differences in SOC stocks between 12 and 25 cm deep non-inversion tillage [55]. For this reason, a reduced tillage depth should be tested at Turda, especially considering the low BD. The mean SOC and MBC stocks were relatively low at Turda, which points towards low C inputs at this site. This would lead to a starving and aged microbial community, as indicated by the relatively low qCO2 values [27,28]. This suggestion was confirmed by a mean metabolic quotient qCO2 of 59 at Turda. Also, the relatively low MBC/SOC ratios with a mean of 1.4% indicate a relatively low C availability to soil microorganisms [28,30]. In addition, strong bonding of relict SOC to clay minerals may further reduce C availability [56]. None of the soil physical (BD), chemical (SOC and total N) and microbial properties (MBC, MBC/SOC and qCO2) were strongly affected by tillage. This could be explained by the fact that both techniques were working at approximately the same depth (Table 1), which indicates that parameters depend more on working depth than on tillage techniques. The field site in Romania was characterised by high SOC concentrations, high clay contents and a low BD. The results from this site indicate that even different tillage techniques can lead to similar microbial conditions, which could by related to the soil type plus the choice of the same working depth for both machineries.

2.4. La Hampa, Spain

At the field site La Hampa, SOC contents were on average 8.7 mg g−1 soil with BD of around 1.31 g cm−3 (Table 1 and Table 2). SOC contents were significantly higher (F = 27.77; p < 0.05) in the upper 10 cm soil depth at NT plots compared with CT (Table 2). Total N contents (mean of 10 mg g−1 soil) were not affected by tillage reduction. MBC contents of NT plots exceeded those of CT plots (Figure 1) in the upper soil layer (F = 30.56; p < 0.05), at 10–20 cm (F = 33.04, p < 0.05) as well as in the lowest soil depth of 20–30 cm (F = 51.07; p < 0.05). The soil was characterised by high sand content and an alkaline soil pH and high MBC/SOC ratios (mean of 2.7%). Increased MBC/SOC ratios with increasing aridity of the climate have been repeatedly observed [57,58], due to shortening of the period for strong microbial activity. Consequently, qCO2 values were low at La Hampa with a range of 31.5 to 64.6 mg CO2 C g−1 MBC d−1, indicating a low demand of the microbial community for maintenance energy. This view is in line with the meta-analysis of Zuber and Villamil [59] who showed that sandy soils have lower qCO2 values under NT than under CT, whereas tillage effects were less in soils with finer particles.
The SOC stocks (mean of 32.5 t ha−1) were relatively low at this site. The latter was significantly greater under NT compared with CT for both, SOC (F = 339.97; p < 0.01) and MBC (F = 50.10; p < 0.05) (Table 3). These higher stocks were combined with a less pronounced depth gradient, which suggests a larger C input rate into the 10–30 cm layers at La Hampa, as proposed by Virto et al. [60]. Another reason for these positive NT effects on SOC and MBC stocks at this semi-arid region might be a slower turnover. Without mechanical disturbance under NT, the mineralisation of aggregate occluded SOC is most likely reduced [61,62]. This lowers the qCO2 values of a starving microbial population [32,63] followed by increased MBC contents and later by a higher contribution of microbial necromass-derived SOC.
Low qCO2 values also indicated that the low SOC stocks at La Hampa are not caused by microbial mineralisation but by low C inputs combined with a low microbial turnover. However, the possibility cannot be excluded that the SOC contents were already different at the start of the experiment, as sandy Fluvisols often exhibit a considerable sedimentation-induced spatial variability [44,57]. This is often not considered, as the initial soil properties are usually analysed by a so-called representative bulk sample, pooled from several cores and not from analysing each plot separately. Results from La Hampa in Spain, where the soil is characterised by a high sand content and an alkaline pH value, showed a strong positive effect of no-till management. This was reflected by higher MBC concentrations and stocks as well as greater SOC stocks. Low qCO2 values and a high MBC/SOC level indicate good conditions for microbial activity.

2.5. Effects among Sites

In general, the application of CT with a mouldboard plough resulted in a more homogeneous distribution of SOC, total N, and MBC contents, due to the strong mixing effect of this tool, whereas MT and especially NT created site-specific depth gradients. This decrease of approximately 30% from the top to the bottom soil layer was similar at Garte Süd and Säby. Hence, confirming our first hypothesis, most effects of reduced tillage on soil parameters were visible at the upper 10 cm soil depth, which was particularly strong at Garte Süd. Stocks of SOC and MBC were 34% higher and 55% lower, respectively, at Säby compared with Garte Süd. The difference in study duration might also explain differences between the site-specific effects. At the German site, reduced tillage was already applied for more than 40 years, whereas at the Swedish site it was just > 10 years. Based on 17 tillage experiments in the study from Smith et al. [64], SOC levels by sequestration needs 50 to 100 years to reach a new equilibrium. These differences are also reflected by the MBC/SOC ratio. Acidification is probably the main reason for the low MBC/SOC ratio at Säby [29], increasing the microbial demand for maintenance energy [45], which is also reflected by the high qCO2 values. In Romania deep non-inversion MT down to 25 cm had no specific positive or negative effects on soil parameters in comparison with CT, suggesting that shallow MT down to 10 cm should be used preferentially.
Contradicting our hypotheses two and three, SOC and MBC stocks were not affected in different ways by tillage. However, the effectiveness of conservation tillage on C stocks was lower than expected. Most evidently, La Hampa was the only site where the SOC and MBC stocks of the NT treatments significantly exceeded those of the CT treatment by 11% and 33%, respectively. SOC stocks at Säby were approximately three times higher, compared with Spain, but MBC stocks were slightly lower due to the acidic soil pH. The main reason for the positive NT effect at La Hampa is most likely the slower turnover of the microbial biomass due to drier climatic conditions, which was also reflected by low qCO2 values, indicating that the low SOC stocks at La Hampa are not the result of strong microbial mineralization.
In line with our fourth hypothesis, the effectiveness of tillage reductions on soil parameters varied strongly between sites. Generally, less effects were found in Sweden, which is mostly related to soil pH and climate. As expected, the differences between the reduced tillage (MT/NT) systems were quite small at Säby. Results indicate that MT also has the potential to improve soil parameters to a similar extent as NT. In contrast, the strong effect of NT at La Hampa implies that no-till techniques are able to enhance microbial soil properties in semi-arid areas in a large extent. Further, marginal differences between tillage treatments in Romania (non-inversion vs. inversion tillage) indicate that soils with high clay contents and a good fertility might generally be affected less by tillage.

3. Material and Methods

3.1. Field Sites Descriptions

Across Europe (Sweden, Germany, Romania, and Spain), four different long-term experimental field sites that focus on tillage were selected for sampling. As CT treatment, inversion mouldboard ploughing down to 30 cm was present in each country, whereas the reduced tillage treatments (MT and/or NT) varied in terms of machinery and working depths (Table 1). All sites are located on flat areas without inclination, so that they could not be affected by water erosion and colluvial processes.
In Sweden, the long-term experimental site Säby is located near Uppsala (59°49′ N 17°42′ E) and was established 11 years before sampling in 2006, using a randomized block design with a plot size of 9 × 20 m and three replicates. The mean annual temperature (MAT) at this site is 6.7 °C with 547 mm mean annual precipitation (MAP) (mean of the years 1988–2017). The soil is an Eutric Cambisol [65] with a soil texture of 25% sand, 52% silt and 23% clay [66] and a pH-H2O of 5.6. The crop rotation consisted of winter wheat (Triticum aestivum L.), oilseed rape (Brassica napus L.), and peas (Pisum sativum L.). Prior to sampling, winter wheat was sown in 2017 and 2016, and peas in 2015. Crop yields were 5.0 t ha−1, 5.6 t ha−1, and 4.2 t ha−1 in 2016, and 9.8 t ha−1, 9.9 t ha−1, and 9.0 t ha−1 in 2015 for CT, MT, and NT, respectively. The soil received mineral fertiliser depending on the cultivated crops, i.e., in total 139 kg N ha−1, 82 kg N ha−1, and 141 kg N ha−1 in the years 2017, 2016, and 2015, respectively.
In Germany, the long-term experimental site Garte Süd is located near Göttingen in southern Lower Saxony (51°29′ N 9°56′ E) and was established 47 years before sampling in 1970. The soil is a Haplic Luvisol [67] with 12% sand, 73% silt, and 15% clay [46] and a pH-H2O of 7.2. Average temperature is 9.5 °C MAT with a precipitation of 621 mm MAP (average from 1989–2018). Plots with a size of 20 × 40 m are arranged in a randomized block design with four replicates. Crop rotations varied inconsistently and were mainly based on cereals. In the two years before sampling, winter wheat (Triticum aestivum L.) in 2016 and a mixture of peas (Pisum sativum L.) and oat (Avena sativa L.) in 2015 were grown on the site. Crop yields were 7.7and 7.4 t ha−1 in 2016 as well as 3.5 and 3.0 t ha−1 in 2015 for CT and MT, respectively. As for fertilisation, Garte Süd received no inorganic fertiliser in 2015, 188 kg N ha−1 in spring 2016, and 207 kg N ha−1 in spring 2017.
In Romania, the long-term experimental site Turda is located near Cluj-Napoca (46°35′ N, 23°48′ E) as a combined tillage and crop rotation experiment with a plot size of 30 × 12 m and three replicates. It was established 11 years before sampling in 2007. The MAT is 9.0 °C at this site with 540 mm MAP [68]. The soil is a Phaeozem with 16% sand, 28% silt and 56% clay as soil texture [69] and a pH-H2O of 7.0. Crop rotations of both tillage systems were soy (Glycine max L.), winter wheat (Triticum aestivum L.), and maize (Zea mays L.). Crop yields were 7.3 and 7.4 t ha−1 in 2016 and 3.2 and 3.3 t ha−1 in 2015 for CT and MT, respectively. The crops were fertilised with 40 kg N ha−1 and 40 kg P ha−1 as complex fertiliser in autumn, while 30 kg N ha−1 was added as NH4NO3 in spring.
In Spain, the field site is part of the experimental farm La Hampa in the southwest near Sevilla (37°17′ N 6°3′ W). The trial was set up 10 years before sampling in 2008 as a randomized block design with a plot size of 14 × 22 m and three replicates per treatment. The average temperature is 19.0 °C MAT with 497 mm MAP [70]. The soil is a Calcic Fluvisol with a pH-H2O of 8.3. Soil texture is 58% sand, 18% silt and 24% clay [16]. The crop rotation contained cereals, sunflowers (Helianthus annuus L.) and legumes. The crops prior to sampling were winter durum wheat (Triticum durum L.) in 2017, broad bean (Vicia faba L.) in 2016 and again winter durum wheat in 2015. In 2016, crop yields were very low at 1.2 t ha−1 for CT and 0.1 t ha−1 for NT, due to extreme weather conditions, but in 2015 they were 4.6 t ha−1 for CT and 2.5 t ha−1 for NT. Wheat received a complex fertiliser at a rate of approximately 60 kg N ha−1, 26 kg P ha−1, and 50 kg K ha−1. Sunflowers and legumes were not fertilised.

3.2. Sampling and Soil Chemical Analysis

Samples were collected from 29 to 30 May 2017 at Garte Süd, from 12 to 22 June 2017 at Säby, from 15 to 25 May 2018 at Turda and on 04 April 2018 at La Hampa from three soil depths (0–10, 10–20, 20–30 cm). In all countries and years, samples were taken under flowering of winter wheat with a soil corer (5 cm diameter and 30 cm length). Four soil samples were taken from each plot and combined for analysis. SOC and total N were analysed from dried, sieved (<2 mm) and ball milled soil samples using a Vario Max CN elemental analyser (Elementar, Hanau, Germany). HCl was added to the soils from Turda and La Hampa to remove inorganic C, for the other field sites total C corresponds to SOC. Soil pH was detected in deionized water with a soil to solution ratio of 1:2.5. BD was calculated by dividing the soil core volume by the soil weight determined after drying the soil at 105 °C.

3.3. Soil Biological Analysis

To determine MBC fumigation extraction [71] was used. Then, 10 g of field-moist soil were extracted pairwise, i.e., fumigated (24 h, ethanol-free CHCl3) and non-fumigated, with 40 mL of 0.05 K2SO4 [72]. Organic C in the extracts was measured using a multi N/C 2100S (Analytik Jena, Jena, Germany). MBC was calculated as EC/kEC, where EC = (organic C from fumigated soil sample)–(organic C from non-fumigated soil sample) and kEC = 0.45 [73]. Basal respiration was determined by the MicroResp method [74]. In brief, the soil was adjusted to a water content of 15% and stored at 22 °C for 3 days before measurements; soil equivalent to 400 mg dry soil was placed in 1.1 mL deep-well microtiter plates and incubated for 6 h in a closed system. The system includes a detection microtiter plate with a colorimetric CO2 trap containing 1% noble agar, 150 mM KCl, 2.5 mM NaHCO3 and 12.5 µg g−1 cresol red. The colour change in the CO2 trap was measured at the beginning (T0) and after 6 h of incubation (T6) at 570 nm with a microplate reader (BioTek, Winooski, USA). The difference in the absorption between T6 and T0 was converted into CO2-C (µg g−1 soil h−1). The metabolic quotient qCO2 was calculated as mg CO2-C g MBC−1 d−1.

3.4. Calculations and Statistical Analyses

Data analyses were carried out using the statistical software R (version 3.6.1, R. Core Team, 2019). Stocks of SOC and MBC were calculated for equivalent soil masses to consider differences in BD [75]. All soil properties presented at 0–10, 10–20, and 20–30 cm as well as MBC and SOC stocks at 0–30 cm were analysed by linear mixed effect models using the package nlme (version 3.1-152, [76]). ‘Tillage’ was used as fixed factor, ‘block’ was considered as random factor. Analysis of variance was performed on the final models for each soil parameter. Residuals of the final model were checked for homoscedasticity. To examine significant differences between groups, a post-hoc test (Tukey test) was carried out, using the package lsmeans (version 2.30-0, [77]). All field sites were evaluated separately from each other. Results of the Romanian field site are presented in a descriptive way, because the experimental field site Turda was originally established as a combined crop and tillage experiment. Due to sampling only under one crop, randomization could not be secured as samples were only taken from winter wheat. Values in the text are given as mean ± standard deviation.

4. Conclusions

Comparing different practises of tillage reductions, our study showed that it is quite important to distinguish between different expressions of conservation tillage. Further, in order to give recommendations for tillage applications, the region, including climate and soil characteristics, has to be considered in each case. Therefore, direct comparison of different sites is limited, and environmental conditions must be considered when evaluating the effectiveness of conservation tillage systems. Especially in regions where agronomical disadvantages of NT could occur, other reduced tillage systems might be preferred without putting soil quality (as indicated by microbial properties) at risk. Therefore, the choice of machinery should also be based on other factors such as fuel consumption or harvest yields. However, our study showed that ploughless tillage systems are recommended as MT and NT resulted in an MBC, C, and N accumulation near the surface independent from site-specific conditions and appeared to have the potential to enhance microbial indicators as well as C stocks in most cases.

Author Contributions

Conceptualization: I.E., M.P.; methodology: I.E., D.L., M.S.; validation: R.G.J., M.P.; formal analysis: I.E.; investigation: I.E.; resources: M.S., C.M.; data curation: I.E., D.L.; writing—original draft preparation: I.E.; writing—review and editing: I.E., D.L., M.S., R.G.J., C.M., M.P.; visualization: I.E.; supervision: D.L., M.P.; project administration: D.L., M.P.; funding acquisition: M.P. All authors have read and agreed to the published version of the manuscript.

Funding

This study (grant number 01LC1620) was funded through the 2015–2016 BiodivERsA COFUND call for research proposals with the national funders Federal Ministry of Education and Research (BMBF/Germany), Development and Innovation Funding (UEFISCDI/Romania), Estonian Research Council (ETAG/Estonia), French National Research Agency (ANR/France), Spanish Ministry of Economy and Competitiveness (MINECO/Spain), Swedish Research Council for Environment, Agricultural Sciences & Spatial Planning (FORMAS/Sweden).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We would like to thank Karin Schmidt for technical assistance as well as Janine Kaus and Jan-Christoph Rattay for help with the experiment. Special thanks to Rahel Sutterlütti for interesting discussions on this work. Furthermore, we thank our colleagues Astrid Taylor and Kaisa Torppa and their team from the SLU in Sweden, the team of Blanca Landa and Gema Guzmán from the IAS-CSIC in Spain, the German team of Christiane Münter from the University of Göttingen and the Romanian team from the USAMV Cluj-Napoca for the support with the field work. The SoilMan project (grant number 01LC1620) was funded through the 2015–2016 BiodivERsA COFUND call for research proposals with the national funders Federal Ministry of Education and Research (BMBF/Germany), Development and Innovation Funding (UEFISCDI/Romania), Estonian Research Council (ETAG/Estonia), French National Research Agency (ANR/France), Spanish Ministry of Economy and Competitiveness (MINECO/Spain), Swedish Research Council for Environment, Agricultural Sciences & Spatial Planning (FORMAS/Sweden).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Van Capelle, C.; Schrader, S.; Brunotte, J. Tillage-induced changes in the functional diversity of soil biota—A review with a focus on German data. Eur. J. Soil Biol. 2012, 50, 165–181. [Google Scholar] [CrossRef]
  2. García-Ruiz, J.M. The effects of land uses on soil erosion in Spain: A review. Catena 2010, 81, 1–11. [Google Scholar] [CrossRef]
  3. Soane, B.D.; van Ouwerkerk, C. (Eds.) Developments in Agricultural Engineering: Soil Compaction in Crop Production; Elsevier: Amsterdam, The Netherlands, 1994; ISBN 0167-4137. [Google Scholar]
  4. Lal, R.; Kimble, J.M. Conservation tillage for carbon sequestration. Nutr. Cycl. Agroecosyst. 1997, 49, 243–253. [Google Scholar] [CrossRef]
  5. Freibauer, A.; Rounsevell, M.D.; Smith, P.; Verhagen, J. Carbon sequestration in the agricultural soils of Europe. Geoderma 2004, 122, 1–23. [Google Scholar] [CrossRef]
  6. Haddaway, N.R.; Hedlund, K.; Jackson, L.E.; Kätterer, T.; Lugato, E.; Thomsen, I.K.; Jørgensen, H.B.; Isberg, P.-E. How does tillage intensity affect soil organic carbon?: A systematic review. Environ. Evid. 2017, 6, 77. [Google Scholar] [CrossRef] [Green Version]
  7. Li, Y.; Li, Z.; Chang, S.X.; Cui, S.; Jagadamma, S.; Zhang, Q.; Cai, Y. Residue retention promotes soil carbon accumulation in minimum tillage systems: Implications for conservation agriculture. Sci. Total Environ. 2020, 740, 140147. [Google Scholar] [CrossRef]
  8. McDonald, M.; Lewis, K.; Ritchie, G. Short term cotton lint yield improvement with cover crop and no-tillage implementation. Agronomy 2020, 10, 994. [Google Scholar] [CrossRef]
  9. Jemai, I.; Aissa, N.; Guirat, S.; Ben-Hammouda, M.; Tahar, G. Impact of three and seven years of no-tillage on the soil water storage, in the plant root zone, under a dry subhumid Tunisian climate. Soil Tillage Res. 2013, 126, 26–33. [Google Scholar] [CrossRef]
  10. Håkansson, I.; Stenberg, M.; Rydberg, T. Long-term experiments with different depths of mouldboard ploughing in Sweden. Soil Tillage Res. 1998, 46, 209–223. [Google Scholar] [CrossRef]
  11. Gonzalez-Sanchez, E.J.; Veroz-Gonzalez, O.; Blanco-Roldan, G.L.; Marquez-Garcia, F.; Carbonell-Bojollo, R. A renewed view of conservation agriculture and its evolution over the last decade in Spain. Soil Tillage Res. 2015, 146, 204–212. [Google Scholar] [CrossRef]
  12. Günal, H.; Korucu, T.; Birkas, M.; Özgöz, E.; Halbac-Cotora-Zamfir, R. Threats to sustainability of soil functions in Central and Southeast Europe. Sustainability 2015, 7, 2161–2188. [Google Scholar] [CrossRef] [Green Version]
  13. Hernández Plaza, E.; Navarrete, L.; González-Andújar, J.L. Intensity of soil disturbance shapes response trait diversity of weed communities: The long-term effects of different tillage systems. Agric. Ecosyst. Environ. 2015, 207, 101–108. [Google Scholar] [CrossRef]
  14. Koch, H.-J.; Dieckmann, J.; Büchse, A.; Märländer, B. Yield decrease in sugar beet caused by reduced tillage and direct drilling. Eur. J. Agron. 2009, 30, 101–109. [Google Scholar] [CrossRef]
  15. Badagliacca, G.; Saia, S.; Ruisi, P.; Amato, G.; Giambalvo, D.; Laudicina, V.A. Microbial biomass carbon dynamics in a long-term tillage and crop rotation experiment under semiarid Mediterranean conditions. Asp. Appl. Biol. 2015, 128, 213–219. [Google Scholar]
  16. López-Garrido, R.; Madejón, E.; León-Camacho, M.; Girón, I.; Moreno, F.; Murillo, J.M. Reduced tillage as an alternative to no-tillage under Mediterranean conditions: A case study. Soil Tillage Res. 2014, 140, 40–47. [Google Scholar] [CrossRef]
  17. Balota, E.L.; Colozzi Filho, A.; Andrade, D.S.; Dick, R.P. Long-term tillage and crop rotation effects on microbial biomass and C and N mineralization in a Brazilian Oxisol. Soil Tillage Res. 2004, 77, 137–145. [Google Scholar] [CrossRef]
  18. Chen, H.; Hou, R.; Gong, Y.; Li, H.; Fan, M.; Kuzyakov, Y. Effects of 11 years of conservation tillage on soil organic matter fractions in wheat monoculture in Loess Plateau of China. Soil Tillage Res. 2009, 106, 85–94. [Google Scholar] [CrossRef]
  19. Heinze, S.; Rauber, R.; Joergensen, R.G. Influence of mouldboard plough and rotary harrow tillage on microbial biomass and nutrient stocks in two long-term experiments on loess derived Luvisols. Appl. Soil Ecol. 2010, 46, 405–412. [Google Scholar] [CrossRef]
  20. Carter, M.R. The influence of tillage on the proportion of organic carbon and nitrogen in the microbial biomass of medium-textured soils in a humid climate. Biol. Fertil. Soils 1991, 11, 135–139. [Google Scholar] [CrossRef]
  21. Andruschkewitsch, R.; Koch, H.-J.; Ludwig, B. Effect of long-term tillage treatments on the temporal dynamics of water-stable aggregates and on macro-aggregate turnover at three German sites. Geoderma 2014, 217–218, 57–64. [Google Scholar] [CrossRef]
  22. Hernanz, J.L.; López, R.; Navarette, L.; Sánchez-Girón, V. Long-term effects of tillage systems and rotations on soil structural stability and organic carbon stratification in semiarid central Spain. Soil Tillage Res. 2002, 66, 129–141. [Google Scholar] [CrossRef]
  23. Morris, N.; Miller, P.; Orson, J.H.; Froud-Williams, R. The adoption of non-inversion tillage systems in the United Kingdom and the agronomic impact on soil, crops and the environment—A review. Soil Tillage Res. 2010, 108, 1–15. [Google Scholar] [CrossRef]
  24. Griffiths, B.S.; Philippot, L. Insights into the resistance and resilience of the soil microbial community. FEMS Microbiol. Rev. 2013, 37, 112–129. [Google Scholar] [CrossRef] [Green Version]
  25. Khan, K.S.; Mack, R.; Castillo, X.; Kaiser, M.; Joergensen, R.G. Microbial biomass, fungal and bacterial residues, and their relationships to the soil organic matter C/N/P/S ratios. Geoderma 2016, 271, 115–123. [Google Scholar] [CrossRef]
  26. Joergensen, R.G.; Wichern, F. Alive and kicking: Why dormant soil microorganisms matter. Soil Biol. Biochem. 2018, 116, 419–430. [Google Scholar] [CrossRef]
  27. Anderson, T.-H.; Domsch, K.H. Application of eco-physiologicai quotients (qCO2 and qD) on microbial biomasses from soils of different cropping histories. Soil Biol. Biochem. 1990, 22, 251–255. [Google Scholar] [CrossRef]
  28. Anderson, T.-H.; Domsch, K.H. Soil microbial biomass: The eco-physiological approach. Soil Biol. Biochem. 2010, 42, 2039–2043. [Google Scholar] [CrossRef]
  29. Anderson, T.; Domsch, K.H. The metabolic quotient for CO2 (qCO2) as a specific activity parameter to assess the effects of environmental conditions, such as pH, on the microbial biomass of forest soils. Soil Biol. Biochem. 1993, 25, 393–395. [Google Scholar] [CrossRef]
  30. Anderson, T.-H.; Domsch, K.H. Ratios of microbial biomass carbon to total organic carbon in arable soils. Soil Biol. Biochem. 1989, 21, 471–479. [Google Scholar] [CrossRef]
  31. Hydbom, S.; Ernfors, M.; Birgander, J.; Hollander, J.; Jensen, E.S.; Olsson, P.A. Reduced tillage stimulated symbiotic fungi and microbial saprotrophs, but did not lead to a shift in the saprotrophic microorganism community structure. Appl. Soil Ecol. 2017, 119, 104–114. [Google Scholar] [CrossRef]
  32. Murugan, R.; Koch, H.-J.; Joergensen, R.G. Long-term influence of different tillage intensities on soil microbial biomass, residues and community structure at different depths. Biol. Fertil. Soils 2014, 50, 487–498. [Google Scholar] [CrossRef]
  33. Frasier, I.; Quiroga, A.; Noellemeyer, E. Effect of different cover crops on C and N cycling in sorghum NT systems. Sci. Total Environ. 2016, 562, 628–639. [Google Scholar] [CrossRef]
  34. Van Groenigen, K.-J.; Bloem, J.; Bååth, E.; Boeckx, P.; Rousk, J.; Bodé, S.; Forristal, D.; Jones, M.B. Abundance, production and stabilization of microbial biomass under conventional and reduced tillage. Soil Biol. Biochem. 2010, 42, 48–55. [Google Scholar] [CrossRef]
  35. Angers, D.A.; Eriksen-Hamel, N.S. Full-Inversion tillage and organic carbon distribution in soil profiles: A meta-analysis. Soil Sci. Soc. Am. J. 2008, 72, 1370–1374. [Google Scholar] [CrossRef]
  36. Du, Z.; Angers, D.A.; Ren, T.; Zhang, Q.; Li, G. The effect of no-till on organic C storage in Chinese soils should not be overemphasized: A meta-analysis. Agric. Ecosyst. Environ. 2017, 236, 1–11. [Google Scholar] [CrossRef]
  37. Jacobs, A.; Rauber, R.; Ludwig, B. Impact of reduced tillage on carbon and nitrogen storage of two Haplic Luvisols after 40 years. Soil Tillage Res. 2009, 102, 158–164. [Google Scholar] [CrossRef]
  38. Jacobs, A.; Jungert, S.; Koch, H.-J. Soil organic carbon as affected by direct drilling and mulching in sugar beet—Wheat rotations. Arch. Agron. Soil Sci. 2015, 61, 1079–1087. [Google Scholar] [CrossRef]
  39. Schjønning, P.; Thomsen, I.K. Shallow tillage effects on soil properties for temperate-region hard-setting soils. Soil Tillage Res. 2013, 132, 12–20. [Google Scholar] [CrossRef]
  40. Struecker, J.; Joergensen, R.G. Microorganisms and their substrate utilization patterns in topsoil and subsoil layers of two silt loams, differing in soil organic C accumulation due to colluvial processes. Soil Biol. Biochem. 2015, 91, 310–317. [Google Scholar] [CrossRef]
  41. Ahl, C.; Joergensen, R.G.; Kandeler, E.; Meyer, B.; Woehler, V. Microbial biomass and activity in silt and sand loams after long-term shallow tillage in central Germany. Soil Tillage Res. 1998, 49, 93–104. [Google Scholar] [CrossRef]
  42. Tian, S.; Ning, T.; Wang, Y.; Liu, Z.; Li, G.; Li, Z.; Lal, R. Crop yield and soil carbon responses to tillage method changes in North China. Soil Tillage Res. 2016, 163, 207–213. [Google Scholar] [CrossRef]
  43. Anderson, T.-H.; Joergensen, R.G. Relationship between SIR and FE estimates of microbial biomass C in deciduous forest soils at different pH. Soil Biol. Biochem. 1997, 29, 1033–1042. [Google Scholar] [CrossRef]
  44. Heinze, S.; Raupp, J.; Joergensen, R.G. Effects of fertilizer and spatial heterogeneity in soil pH on microbial biomass indices in a long-term field trial of organic agriculture. Plant Soil 2010, 328, 203–215. [Google Scholar] [CrossRef]
  45. Malik, A.A.; Puissant, J.; Buckeridge, K.M.; Goodall, T.; Jehmlich, N.; Chowdhury, S.; Gweon, H.S.; Peyton, J.M.; Mason, K.E.; van Agtmaal, M.; et al. Land use driven change in soil pH affects microbial carbon cycling processes. Nat. Commun. 2018, 9, 3591. [Google Scholar] [CrossRef]
  46. Ehlers, W.; Werner, D.; Mähner, T. Wirkung mechanischer Belastung auf Gefüge und Ertragsleistung einer Löss-Parabraunerde mit zwei Bearbeitungssystemen. J. Plant Nutr. Soil Sci. 2000, 163, 321–333. [Google Scholar] [CrossRef]
  47. Lamandé, M.; Greve, M.H.; Schjønning, P. Risk assessment of soil compaction in Europe—Rubber Tracks or Wheels on Machinery. Catena 2018, 167, 353–362. [Google Scholar] [CrossRef]
  48. Unger, P.W.; Kaspar, T.C. Soil compaction and root growth: A review. Agron. J. 1994, 86, 759–766. [Google Scholar] [CrossRef]
  49. Ştefan, C.; Ştefan, G. An overview on the main properties of a gleyic Phaeozem located in Mitroc, Botosani Country, Romania. Sci. Papers. Ser. A Agron. 2012, 55, 117–120. [Google Scholar]
  50. Blair, N.; Faulkner, R.D.; Till, A.R.; Poulton, P.R. Long-term management impacts on soil C, N and physical fertility. Soil Tillage Res. 2006, 91, 30–38. [Google Scholar] [CrossRef]
  51. Kravchenko, Y.; Rogovska, N.; Petrenko, L.; Zhang, X.; Song, C.; Chen, Y. Quality and dynamics of soil organic matter in a typical Chernozem of Ukraine under different long-term tillage systems. Can. J. Soil. Sci. 2012, 92, 429–438. [Google Scholar] [CrossRef] [Green Version]
  52. Bonetti, J.d.; Anghinoni, I.; de Moraes, M.T.; Fink, J.R. Resilience of soils with different texture, mineralogy and organic matter under long-term conservation systems. Soil Tillage Res. 2017, 174, 104–112. [Google Scholar] [CrossRef]
  53. Gregory, A.S.; Watts, C.W.; Whalley, W.R.; Kuan, H.L.; Griffiths, B.S.; Hallett, P.D.; Whitmore, A.P. Physical resilience of soil to field compaction and the interactions with plant growth and microbial community structure. Eur. J. Soil Sci. 2007, 58, 1221–1232. [Google Scholar] [CrossRef]
  54. 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. [Google Scholar] [CrossRef]
  55. Cooper, J.; Baranski, M.; Stewart, G.; Nobel-de Lange, M.; Bàrberi, P.; Fließbach, A.; Peigné, J.; Berner, A.; Brock, C.; Casagrande, M.; et al. Shallow non-inversion tillage in organic farming maintains crop yields and increases soil C stocks: A meta-analysis. Agron. Sustain. Dev. 2016, 36, 22. [Google Scholar] [CrossRef]
  56. Sarkar, B.; Singh, M.; Mandal, S.; Churchman, G.J.; Bolan, N.S. Clay minerals—Organic matter interactions in relation to carbon stabilization in soils. In The Future of Soil Carbon: Its Conservation and Formation; Garcia, C., Nannipieri, P., Hernandez, T., Eds.; Elsevier: London, UK, 2018; pp. 71–86. ISBN 9780128116876. [Google Scholar]
  57. Goenster, S.; Gründler, C.; Buerkert, A.; Joergensen, R.G. Soil microbial indicators across land use types in the river oasis Bulgan sum center, Western Mongolia. Ecol. Indic. 2017, 76, 111–118. [Google Scholar] [CrossRef]
  58. Wichern, F.; Joergensen, R.G. Soil microbial properties along a precipitation transect in Southern Africa. Arid. Land Res. Manag. 2009, 23, 115–126. [Google Scholar] [CrossRef]
  59. Zuber, S.M.; Villamil, M.B. Meta-analysis approach to assess effect of tillage on microbial biomass and enzyme activities. Soil Biol. Biochem. 2016, 97, 176–187. [Google Scholar] [CrossRef] [Green Version]
  60. Virto, I.; Barré, P.; Burlot, A.; Chenu, C. Carbon input differences as the main factor explaining the variability in soil organic C storage in no-tilled compared to inversion tilled agrosystems. Biogeochemistry 2012, 108, 17–26. [Google Scholar] [CrossRef]
  61. Helgason, B.L.; Walley, F.L.; Germida, J.J. No-till soil management increases microbial biomass and alters community profiles in soil aggregates. Appl. Soil Ecol. 2010, 46, 390–397. [Google Scholar] [CrossRef]
  62. Zhang, Y.; Zhang, Z.; Ma, Z.; Chen, J.; Akbar, J.; Zhang, S.; Che, C.; Zhang, M.; Cerdà, A.; Lupwayi, N. A review of preferential water flow in soil science. Can. J. Soil Sci. 2018, 98, 604–618. [Google Scholar] [CrossRef]
  63. Faust, S.; Koch, H.-J.; Joergensen, R.G. Respiration response to different tillage intensities in transplanted soil columns. Geoderma 2019, 352, 289–297. [Google Scholar] [CrossRef]
  64. Smith, P.; Powlson, D.; Glendining, M.; Smith, J. Preliminary estimates of the potential for carbon mitigation in European soils through no-till farming. Glob. Change Biol. 1998, 4, 679–685. [Google Scholar] [CrossRef]
  65. Etana, A.; Rydberg, T.; Arvidsson, J. Readily dispersible clay and particle transport in five Swedish soils under long-term shallow tillage and mouldboard ploughing. Soil Tillage Res. 2009, 106, 79–84. [Google Scholar] [CrossRef]
  66. Arvidsson, J. Energy use efficiency in different tillage systems for winter wheat on a clay and silt loam in Sweden. Eur. J. Agron. 2010, 33, 250–256. [Google Scholar] [CrossRef]
  67. Reiter, K.; Schmidtke, K.; Rauber, R. The influence of long-term tillage systems on symbiotic N2 fixation of pea (Pisum sativum L.) and red clover (Trifolium pratense L.). Plant Soil 2002, 238, 41–55. [Google Scholar] [CrossRef]
  68. Chetan, F. Pretabilitatea Rotației Soia-Grâu-Porumb la Cultivarea în Sistemul de Conservare a Însușirilor Solului Pentru Zonele Culinare cu Agresivitate Hidrică Medie. Ph.D. Thesis, Universitatea de Științe Agricole și Medicină Veterinară (USAMV), Cluj-Napoca, Romania, 2015. [Google Scholar]
  69. Chetan, F. Cercetări Privind Aplicabilitatea Sistemelor Conservative de Lucrări ale Solului la SCDA Turda. In Contribuții ale Cercetării Științifice la Dezvoltarea Agriculturii; Tritean, N., Muresan, F., Moldovan, V., Eds.; Revista Agricultura Transilvana: Cluj, Romania, 2017; Volume VII. [Google Scholar]
  70. Panettieri, M.; Berns, A.E.; Knicker, H.; Murillo, J.M.; Madejón, E. Evaluation of seasonal variability of soil biogeochemical properties in aggregate-size fractioned soil under different tillages. Soil Tillage Res. 2015, 151, 39–49. [Google Scholar] [CrossRef] [Green Version]
  71. Vance, E.D.; Brookes, P.C.; Jenkinson, D.S. An extraction method for measuring soil microbial biomass C. Soil Biol. Biochem. 1987, 19, 703–707. [Google Scholar] [CrossRef]
  72. Engelking, B.; Flessa, H.; Joergensen, R.G. Microbial use of maize cellulose and sugarcane sucrose monitored by changes in the 13C/12C ratio. Soil Biol. Biochem. 2007, 39, 1888–1896. [Google Scholar] [CrossRef]
  73. Wu, J.; Joergensen, R.G.; Pommerening, B.; Chaussod, R. Measurement of soil microbial biomass C by fumigation-extraction—an automated procedure. Soil Biol. Biochem. 1990, 22, 1167–1169. [Google Scholar] [CrossRef]
  74. Campbell, C.D.; Chapman, S.J.; Cameron, C.M.; Davidson, M.S.; Potts, J.M. A rapid microtiter plate method to measure carbon dioxide evolved from carbon substrate amendments so as to determine the physiological profiles of soil microbial communities by using whole soil. Appl. Environ. Microbiol. 2003, 69, 3593–3599. [Google Scholar] [CrossRef] [Green Version]
  75. Ellert, B.H.; Bettany, J.R. Calculation of organic matter and nutrients stored in soils under contrasting management regimes. Can. J. Soil Sci. 1995, 75, 529–538. [Google Scholar] [CrossRef] [Green Version]
  76. Pinheiro, J.; Bates, D.; DebRoy, S.; Sarkar, D.; R Core Team. nlme: Linear and Nonlinear Mixed Effects Models: R package version 3.1-145. Available online: https://CRAN.R-project.org/package=nlme (accessed on 29 August 2021).
  77. Lenth, R.V. Least-Squares Means: The R Package lsmeans. J. Stat. Softw. 2016, 69, 1–33. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Effect of tillage treatments (CT = Conventional tillage, MT = Minimum tillage, NT = No-tillage) in Germany (n = 4), Romania (n = 3), Spain (n = 3) and Sweden (n = 3) on soil microbial biomass carbon at the soil depths (0–10 cm, 10–20 cm, 20–30 cm) given as means ± standard deviation. Means followed by different letters (a, b) are significantly (p < 0.05) different from each other at each soil depth. Tillage treatments were carried out in a site-specific way (Table 1).
Figure 1. Effect of tillage treatments (CT = Conventional tillage, MT = Minimum tillage, NT = No-tillage) in Germany (n = 4), Romania (n = 3), Spain (n = 3) and Sweden (n = 3) on soil microbial biomass carbon at the soil depths (0–10 cm, 10–20 cm, 20–30 cm) given as means ± standard deviation. Means followed by different letters (a, b) are significantly (p < 0.05) different from each other at each soil depth. Tillage treatments were carried out in a site-specific way (Table 1).
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Engell, I.; Linsler, D.; Sandor, M.; Joergensen, R.G.; Meinen, C.; Potthoff, M. The Effects of Conservation Tillage on Chemical and Microbial Soil Parameters at Four Sites across Europe. Plants 2022, 11, 1747. https://doi.org/10.3390/plants11131747

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Engell I, Linsler D, Sandor M, Joergensen RG, Meinen C, Potthoff M. The Effects of Conservation Tillage on Chemical and Microbial Soil Parameters at Four Sites across Europe. Plants. 2022; 11(13):1747. https://doi.org/10.3390/plants11131747

Chicago/Turabian Style

Engell, Ilka, Deborah Linsler, Mignon Sandor, Rainer Georg Joergensen, Catharina Meinen, and Martin Potthoff. 2022. "The Effects of Conservation Tillage on Chemical and Microbial Soil Parameters at Four Sites across Europe" Plants 11, no. 13: 1747. https://doi.org/10.3390/plants11131747

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