Humus on the Rocks—Water Storage Capacity of Tangelhumus is Essential for Water Retention in Limestone Mountains

IF 2.8 3区 农林科学 Q1 AGRONOMY
Axel Göttlein, Michael Kohlpaintner
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In addition, the pedological classification of rock-humus soils is not straightforward. In the WRB classification system, they are largely classified as Folic Histosols, but can also be found within the group of Leptosols (Leitgeb et al. <span>2013</span>). National classification systems often vary considerably in how they categorise these soils. In Bavaria, for example, they can be found under the designations Felshumusböden (rock-humus soil) and O/C-Böden (O/C soil; O for organic, C for parent material of soil development) (LfU <span>2017</span>). What all rock-humus soils have in common is that their ecology is determined exclusively by the humus layer. It serves as the only rooting zone, nutrient store and water store. If the humus layer disappears, bare rock remains. Due to their unique formation conditions, the properties of the humus layers over rock differ significantly from those of typical humus layers of mineral soils. For this reason, they are classified in a separate humus class, which is widely referred to as Tangelhumus (Kolb and Göttlein <span>2021</span>). In the Bavarian Alps, Tangel-humus preferentially forms over solid or coarse carbonate rocks with low residual clay content and can reach a thickness of more than 100 cm. It is mainly found in the montane to subalpine zone of the Limestone Alps, where a cool and humid climate favours the accumulation of organic matter (Kolb and Kohlpaintner <span>2018</span>). However, such humus layers can be found not only on calcareous but also on acidic bedrock, showing expected differences in pH and cation composition at the contact zone with the respective bedrock (Kolb and Göttlein <span>2022</span>; Stolarczyk et al. <span>2024</span>). In addition to chemical properties, understanding the water storage capacity of Tangelhumus is crucial, both for estimating the water supply of the trees and for assessing the landscape water regimes. Extensive tables are available for the water storage capacity of mineral soil horizons, differentiated by texture, bulk density and humus content (AK Standortskartierung <span>2016</span>). However, such values are not available for Tangelhumus horizons. Therefore, pF curves were derived for Tangelhumus horizons of the Bavarian Limestone Alps, which allowing for quantification of the storage potential for plant-available water (plant available water capacity, PAWC) and the total water retention (field capacity, FC).</p><p>In the Bavarian Limestone Alps, three sites with Tangelhumus were sampled (Figure 1). The Simetsberg site, a mixed mountain forest (beech, spruce, maple, fir), is located in the Werdenfelser Land near lake Walchensee at an altitude of 927 m. The pure Norway spruce stand Lange Au is situated in the Mangfallgebirge close to lake Tegernsee at 943 m asl. In the Berchtesgadener Alpen, the Lattenberg site is a Norway spruce forest at 1436 m asl. The bedrock of Simetsberg and Lange Au is dolomite (Hauptdolomit) and that of Lattenberg is limestone (Dachsteinkalk).</p><p>The pF curves were determined using the HYPROP and WP4C analysers from METER (Munich). The HYPROP method is based on the evaporation method according to Schindler (<span>1980</span>). The measuring range was extended by Schindler et al. (<span>2010</span>) and ranges from water saturation to near the permanent wilting point (pF 4.2). Values around and above pF 4.2 were measured with the WP4C dew point potentiometer. For the analyses, undisturbed sample cylinders (diameter 8 cm, height 5 cm) were taken from Tangelhumus horizons, each with a volume of 250 cm<sup>3</sup>.</p><p>Sampling proved challenging, as obtaining intact sample cylinders from the often densely rooted Tangelhumus profiles is difficult. The measurement of the water tension curve with HYPROP typically took between 15 and 22 days, with some samples requiring up to 38 days. During this time, continuous contact between the shrinking sample and the built-in minitensiometer had to be maintained, and if contact was lost the measurement and sample were discarded. On average, the total processing time for a single sample required 3–4 weeks.</p><p>In the laboratory, samples were fully saturated with water and placed in the HYPROP system. Measurement progress was monitored, and data were recorded using the HYPROP-View software (METER). The pF curves were modelled by integrating the WP4C measurements with the HYPROP-FIT software (METER; Pertassek et al. <span>2015</span>) using the ‘unconstrained van Genuchten-Mualem’ method.</p><p>To estimate the importance of the humus layer to the landscape water budget, a simple model based on the method proposed by Haude (<span>1952</span>) was used to calculate the evapotranspiration of a virtual coniferous stand on humus layers of different thickness using the formulae and tables given in BGR (<span>2000</span>). Although the Haude method is easy to use and requires only few input data, it gives quite good results (DVWK <span>1996</span>). Meteorological data from the Mittenwald-Buckelwiesen weather station (station number 3307) near the Simetsberg site were used to run the model on a daily basis. For this station, the German weather service (DWD) provides quality-controlled open data for the years 1937–2022 (https://opendata.dwd.de). To represent the range of possible water balances, the years with the warmest (2003), driest (1947), coolest (1974) and wettest (1966) growing seasons (May–October) were selected for analysis.</p><p>Figure 2 shows the modelled water tension curve and the characteristic values derived for an Oh horizon. The values for all measured samples are listed in Table 1. Total pore volume (TPV) ranges between 80.5% and 89.9% and air capacity (AC) between 17.4% and 30.2%. FC ranges from 56.3% to 71.9% and PAWC from 40.6% to 59.8%. At the Simetsberg site, all relevant Tangelhumus horizons could be sampled. However, there was no clear trend in the measured values with developing humification from Of to Oh to Ovh. Deviations within a horizon (measured for Oh) and between sites were generally greater than differences due to humification. Thus, the mean values given in Table 1 provide a good estimate of the water-holding capacity across an entire Tangelhumus profile.</p><p>Compared to silt, the mineral soil with the highest PAWC, Tangelhumus horizons have a TPV nearly twice as high, a PAWC more than twice as high and a much higher AC. Only raised bog peat exhibits higher values than Tangelhumus (Table 1). However, the measured values for the Ovh-horizon at Lange Au come very close to the values reported for raised bog peat.</p><p>The very high water storage capacity can lead to water stagnation, particularly in the Ovh-horizon, during the heavy precipitation events typical for the Alpine region. This effect is likely intensified by an additional capillary barrier at the transition to the underlying parent material. The resulting temporary oxygen deficiency, combined with the rather cool temperatures, leads to impaired decomposition conditions and could therefore be an important stabilising factor for Tangelhumus layers.</p><p>Using the average values for each site from Table 1 and the average Tangelhumus thickness at each site, the storage capacity for plant available water can be estimated (Table 2). These high values ensure a good water supply for the forest stand and a high storage capacity during heavy rainfall events. However, climate change, with rising temperatures, fewer wet periods and persistently high nitrogen inputs, promotes mineralisation and thus leads to a gradual degradation of Tangelhumus (Gangkofner and Göttlein <span>2014</span>). This degradation of humus reduces the available rooting space of humus-dominated forest sites, reduces their water-holding capacity and, in extreme cases, even harms their forest viability.</p><p>Estimating the water budget based on humus layer thickness with a simple model (Figure 3) reveals some interesting aspects. When evapotranspiration of the stand no longer can be satisfied by the plant available water of the humus layer, the model computes a transpiration deficit. For the warmest and driest year as well as for the coldest and wettest year, the calculated curves of transpiration deficit are very close together. The arrows given in Figure 3 indicate the humus thickness below which the model calculates seven or more consecutive days of water deficit for the stand. Due to the high PAWC of Tangelhumus, in combination with high precipitation in the Bavarian Alps in cold and wet years, 6 cm of humus is enough to provide the stand with water. In warm and dry years, at least 17 cm is needed. Over the long term, this implies that stands with a humus thickness below 17 cm are susceptible to drought, and that the thinner the humus layer, the lower the chance of forest survival. This threshold value of about 17 cm is supported by unpublished data from a study where we measured humus thickness in 24 forested Tangelhumus sites, spruce forests and mixed mountain forests, in Allgäu, Werdenfelser Land, Mangfallgebirge and Berchtesgadener Alpen regions, totalling 344 measurements. Only two measurements, 12 and 16 cm, were lower than the above-mentioned threshold. Lower values, however, are found in degrading forests.</p><p>Figure 3 also shows the estimated seepage depending on humus thickness. In cool and wet years, seepage remains nearly constant down to a humus thickness of about 6 cm, because water loss by evapotranspiration is quickly compensated by precipitation and the humus layer remains saturated most of the time. In warm and dry years, seepage gradually increases from 50 cm down to 6 cm thickness, because the humus storage capacity is not fully used, and as a consequence seepage becomes dependent on humus thickness. Below 6 cm, seepage increases dramatically as humus thickness decreases towards 0 cm, because finally there is no longer any humus to store water or vegetation to utilise it through evapotranspiration. Transforming a humus rock soil into bare rock results in a fast and nearly quantitative seepage of every rain event. Comparing seepage at 17 cm humus, the thickness at which a mountain forest can just about survive also in dry years, with a completely degraded site (0 cm humus) for all four modelled years there is a dramatic increase in seepage of more than 500 mm. For comparison, this value is about the total annual precipitation of Würzburg (1971–2000: 583 mm; Würzburg-Heidingsfeld; open data DWD).</p><p>As shown in Figure 1, the proportion of forests growing on Tangelhumus ranges from 5% to 19%, with the lowest value in Allgäu and the highest value in the Berchtesgadener Alpen. The vitality of forests on Tangelhumus is therefore of great importance for water retention in the landscape. If these forests are threatened by disasters such as windthrow, bark beetle or the degradation of Tangelhumus due to a warming climate, their protective functions against avalanches and rockfall can, at least partially, be compensated by technical measures such as avalanche barriers or rockfall fences. 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引用次数: 0

Abstract

Rock-humus soils are found primarily in mountainous areas, where they are an important part of the soil landscape. Since they often only occur in small areas, their importance is frequently underestimated on large-scale maps. For example, this soil class is not shown at all on the 1:1,000,000 scale soil map of Europe (Panagos 2006), not even in mountainous regions. This is despite the fact that in the Bavarian Alps, rock-humus soils account for around 10% of the landscape (Olleck et al. 2021; cf. Figure 1). In the Polish part of the Tatra Mountains, a proportion of approximately 3.5% has been reported (Stolarczyk et al. 2024). In addition, the pedological classification of rock-humus soils is not straightforward. In the WRB classification system, they are largely classified as Folic Histosols, but can also be found within the group of Leptosols (Leitgeb et al. 2013). National classification systems often vary considerably in how they categorise these soils. In Bavaria, for example, they can be found under the designations Felshumusböden (rock-humus soil) and O/C-Böden (O/C soil; O for organic, C for parent material of soil development) (LfU 2017). What all rock-humus soils have in common is that their ecology is determined exclusively by the humus layer. It serves as the only rooting zone, nutrient store and water store. If the humus layer disappears, bare rock remains. Due to their unique formation conditions, the properties of the humus layers over rock differ significantly from those of typical humus layers of mineral soils. For this reason, they are classified in a separate humus class, which is widely referred to as Tangelhumus (Kolb and Göttlein 2021). In the Bavarian Alps, Tangel-humus preferentially forms over solid or coarse carbonate rocks with low residual clay content and can reach a thickness of more than 100 cm. It is mainly found in the montane to subalpine zone of the Limestone Alps, where a cool and humid climate favours the accumulation of organic matter (Kolb and Kohlpaintner 2018). However, such humus layers can be found not only on calcareous but also on acidic bedrock, showing expected differences in pH and cation composition at the contact zone with the respective bedrock (Kolb and Göttlein 2022; Stolarczyk et al. 2024). In addition to chemical properties, understanding the water storage capacity of Tangelhumus is crucial, both for estimating the water supply of the trees and for assessing the landscape water regimes. Extensive tables are available for the water storage capacity of mineral soil horizons, differentiated by texture, bulk density and humus content (AK Standortskartierung 2016). However, such values are not available for Tangelhumus horizons. Therefore, pF curves were derived for Tangelhumus horizons of the Bavarian Limestone Alps, which allowing for quantification of the storage potential for plant-available water (plant available water capacity, PAWC) and the total water retention (field capacity, FC).

In the Bavarian Limestone Alps, three sites with Tangelhumus were sampled (Figure 1). The Simetsberg site, a mixed mountain forest (beech, spruce, maple, fir), is located in the Werdenfelser Land near lake Walchensee at an altitude of 927 m. The pure Norway spruce stand Lange Au is situated in the Mangfallgebirge close to lake Tegernsee at 943 m asl. In the Berchtesgadener Alpen, the Lattenberg site is a Norway spruce forest at 1436 m asl. The bedrock of Simetsberg and Lange Au is dolomite (Hauptdolomit) and that of Lattenberg is limestone (Dachsteinkalk).

The pF curves were determined using the HYPROP and WP4C analysers from METER (Munich). The HYPROP method is based on the evaporation method according to Schindler (1980). The measuring range was extended by Schindler et al. (2010) and ranges from water saturation to near the permanent wilting point (pF 4.2). Values around and above pF 4.2 were measured with the WP4C dew point potentiometer. For the analyses, undisturbed sample cylinders (diameter 8 cm, height 5 cm) were taken from Tangelhumus horizons, each with a volume of 250 cm3.

Sampling proved challenging, as obtaining intact sample cylinders from the often densely rooted Tangelhumus profiles is difficult. The measurement of the water tension curve with HYPROP typically took between 15 and 22 days, with some samples requiring up to 38 days. During this time, continuous contact between the shrinking sample and the built-in minitensiometer had to be maintained, and if contact was lost the measurement and sample were discarded. On average, the total processing time for a single sample required 3–4 weeks.

In the laboratory, samples were fully saturated with water and placed in the HYPROP system. Measurement progress was monitored, and data were recorded using the HYPROP-View software (METER). The pF curves were modelled by integrating the WP4C measurements with the HYPROP-FIT software (METER; Pertassek et al. 2015) using the ‘unconstrained van Genuchten-Mualem’ method.

To estimate the importance of the humus layer to the landscape water budget, a simple model based on the method proposed by Haude (1952) was used to calculate the evapotranspiration of a virtual coniferous stand on humus layers of different thickness using the formulae and tables given in BGR (2000). Although the Haude method is easy to use and requires only few input data, it gives quite good results (DVWK 1996). Meteorological data from the Mittenwald-Buckelwiesen weather station (station number 3307) near the Simetsberg site were used to run the model on a daily basis. For this station, the German weather service (DWD) provides quality-controlled open data for the years 1937–2022 (https://opendata.dwd.de). To represent the range of possible water balances, the years with the warmest (2003), driest (1947), coolest (1974) and wettest (1966) growing seasons (May–October) were selected for analysis.

Figure 2 shows the modelled water tension curve and the characteristic values derived for an Oh horizon. The values for all measured samples are listed in Table 1. Total pore volume (TPV) ranges between 80.5% and 89.9% and air capacity (AC) between 17.4% and 30.2%. FC ranges from 56.3% to 71.9% and PAWC from 40.6% to 59.8%. At the Simetsberg site, all relevant Tangelhumus horizons could be sampled. However, there was no clear trend in the measured values with developing humification from Of to Oh to Ovh. Deviations within a horizon (measured for Oh) and between sites were generally greater than differences due to humification. Thus, the mean values given in Table 1 provide a good estimate of the water-holding capacity across an entire Tangelhumus profile.

Compared to silt, the mineral soil with the highest PAWC, Tangelhumus horizons have a TPV nearly twice as high, a PAWC more than twice as high and a much higher AC. Only raised bog peat exhibits higher values than Tangelhumus (Table 1). However, the measured values for the Ovh-horizon at Lange Au come very close to the values reported for raised bog peat.

The very high water storage capacity can lead to water stagnation, particularly in the Ovh-horizon, during the heavy precipitation events typical for the Alpine region. This effect is likely intensified by an additional capillary barrier at the transition to the underlying parent material. The resulting temporary oxygen deficiency, combined with the rather cool temperatures, leads to impaired decomposition conditions and could therefore be an important stabilising factor for Tangelhumus layers.

Using the average values for each site from Table 1 and the average Tangelhumus thickness at each site, the storage capacity for plant available water can be estimated (Table 2). These high values ensure a good water supply for the forest stand and a high storage capacity during heavy rainfall events. However, climate change, with rising temperatures, fewer wet periods and persistently high nitrogen inputs, promotes mineralisation and thus leads to a gradual degradation of Tangelhumus (Gangkofner and Göttlein 2014). This degradation of humus reduces the available rooting space of humus-dominated forest sites, reduces their water-holding capacity and, in extreme cases, even harms their forest viability.

Estimating the water budget based on humus layer thickness with a simple model (Figure 3) reveals some interesting aspects. When evapotranspiration of the stand no longer can be satisfied by the plant available water of the humus layer, the model computes a transpiration deficit. For the warmest and driest year as well as for the coldest and wettest year, the calculated curves of transpiration deficit are very close together. The arrows given in Figure 3 indicate the humus thickness below which the model calculates seven or more consecutive days of water deficit for the stand. Due to the high PAWC of Tangelhumus, in combination with high precipitation in the Bavarian Alps in cold and wet years, 6 cm of humus is enough to provide the stand with water. In warm and dry years, at least 17 cm is needed. Over the long term, this implies that stands with a humus thickness below 17 cm are susceptible to drought, and that the thinner the humus layer, the lower the chance of forest survival. This threshold value of about 17 cm is supported by unpublished data from a study where we measured humus thickness in 24 forested Tangelhumus sites, spruce forests and mixed mountain forests, in Allgäu, Werdenfelser Land, Mangfallgebirge and Berchtesgadener Alpen regions, totalling 344 measurements. Only two measurements, 12 and 16 cm, were lower than the above-mentioned threshold. Lower values, however, are found in degrading forests.

Figure 3 also shows the estimated seepage depending on humus thickness. In cool and wet years, seepage remains nearly constant down to a humus thickness of about 6 cm, because water loss by evapotranspiration is quickly compensated by precipitation and the humus layer remains saturated most of the time. In warm and dry years, seepage gradually increases from 50 cm down to 6 cm thickness, because the humus storage capacity is not fully used, and as a consequence seepage becomes dependent on humus thickness. Below 6 cm, seepage increases dramatically as humus thickness decreases towards 0 cm, because finally there is no longer any humus to store water or vegetation to utilise it through evapotranspiration. Transforming a humus rock soil into bare rock results in a fast and nearly quantitative seepage of every rain event. Comparing seepage at 17 cm humus, the thickness at which a mountain forest can just about survive also in dry years, with a completely degraded site (0 cm humus) for all four modelled years there is a dramatic increase in seepage of more than 500 mm. For comparison, this value is about the total annual precipitation of Würzburg (1971–2000: 583 mm; Würzburg-Heidingsfeld; open data DWD).

As shown in Figure 1, the proportion of forests growing on Tangelhumus ranges from 5% to 19%, with the lowest value in Allgäu and the highest value in the Berchtesgadener Alpen. The vitality of forests on Tangelhumus is therefore of great importance for water retention in the landscape. If these forests are threatened by disasters such as windthrow, bark beetle or the degradation of Tangelhumus due to a warming climate, their protective functions against avalanches and rockfall can, at least partially, be compensated by technical measures such as avalanche barriers or rockfall fences. However, there is no feasible technical substitute for their role in water retention.

Abstract Image

岩石上的腐殖质——黄杨腐殖质的蓄水能力对石灰岩山区的蓄水至关重要
岩石腐殖质土壤主要存在于山区,是土壤景观的重要组成部分。由于它们通常只出现在小区域,因此在大比例尺地图上它们的重要性经常被低估。例如,在欧洲1:1万比例尺的土壤地图(Panagos 2006)上根本没有显示这种土壤类别,甚至在山区也没有。尽管在巴伐利亚阿尔卑斯山,岩石腐殖质土壤占景观的10%左右(Olleck et al. 2021;参见图1)。在塔特拉山脉的波兰部分,报告的比例约为3.5% (Stolarczyk et al. 2024)。此外,岩石-腐殖质土壤的土壤学分类并不简单。在WRB分类系统中,它们主要被归类为Folic Histosols,但也可以在Leptosols组中找到(Leitgeb et al. 2013)。各国的分类系统在如何对这些土壤进行分类方面往往差别很大。例如,在巴伐利亚,它们可以在Felshumusböden(岩石腐殖质土壤)和O/C-Böden (O/C土壤)的名称下找到;O代表有机,C代表土壤发育母质)(LfU 2017)。所有岩石-腐殖质土壤的共同之处在于它们的生态完全由腐殖质层决定。它是唯一的生根区、养分储藏库和水分储藏库。如果腐殖质层消失,剩下的是裸露的岩石。由于其独特的形成条件,岩石上的腐殖质层的性质与矿物土壤中典型的腐殖质层有很大的不同。因此,它们被分类在一个单独的腐殖质类中,被广泛地称为Tangelhumus (Kolb和Göttlein 2021)。在巴伐利亚阿尔卑斯山脉,坦格-腐殖质优先形成于固体或粗糙的碳酸盐岩上,残余粘土含量低,厚度可达100厘米以上。它主要存在于石灰岩阿尔卑斯山脉的山地到亚高山地带,那里凉爽潮湿的气候有利于有机质的积累(Kolb和Kohlpaintner 2018)。然而,这种腐殖质层不仅可以在钙质基岩上发现,也可以在酸性基岩上发现,在接触带与各自基岩的pH和阳离子组成存在预期的差异(Kolb和Göttlein 2022;Stolarczyk et al. 2024)。除了化学性质外,了解Tangelhumus的储水能力对于估计树木的供水和评估景观水状况至关重要。根据质地、体积密度和腐殖质含量的不同,矿质土壤层的储水能力有广泛的表格可供选择(AK Standortskartierung 2016)。然而,这些值并不适用于Tangelhumus的视界。因此,对巴伐利亚石灰岩阿尔卑斯山脉的Tangelhumus层导出了pF曲线,从而可以量化植物有效水的储存潜力(植物有效水容量,PAWC)和总保水能力(田间容量,FC)。在巴伐利亚石灰石阿尔卑斯山脉,对三个地点进行了取样(图1)。Simetsberg遗址是一个混合山林(山毛榉、云杉、枫树、冷杉),位于海拔927米的Walchensee湖附近的Werdenfelser Land。纯挪威云杉林Lange Au位于海拔943米的Tegernsee湖附近的Mangfallgebirge。在Berchtesgadener Alpen, Lattenberg遗址是海拔1436米的挪威云杉林。Simetsberg和Lange Au的基岩为白云岩(Hauptdolomit), Lattenberg的基岩为石灰岩(Dachsteinkalk)。pF曲线采用METER (Munich)的HYPROP和WP4C分析仪测定。HYPROP方法是基于Schindler(1980)的蒸发法。Schindler et al.(2010)扩大了测量范围,从含水饱和度到永久萎蔫点附近(pF 4.2)。用WP4C露点电位器测量pF 4.2左右及以上的值。为了进行分析,未受干扰的样品柱(直径8厘米,高度5厘米)从Tangelhumus地平线上取下,每个体积为250 cm3。采样被证明是具有挑战性的,因为从经常密集扎根的Tangelhumus剖面中获得完整的样品柱是困难的。使用HYPROP测量水张力曲线通常需要15至22天,有些样品需要长达38天。在此期间,必须保持收缩样品与内置最小张力计之间的连续接触,如果失去接触,则丢弃测量和样品。平均而言,单个样品的总处理时间需要3-4周。在实验室中,样品被水完全饱和并放置在HYPROP系统中。监测测量进度,并使用HYPROP-View软件(METER)记录数据。通过将WP4C测量值与HYPROP-FIT软件(METER;Pertassek et al. 2015)使用“无约束van Genuchten-Mualem”方法。 为了估计腐殖质层对景观水分平衡的重要性,采用Haude(1952)提出的简单模型,利用BGR(2000)给出的公式和表格,计算了不同厚度腐殖质层上虚拟针叶林的蒸散量。虽然Haude方法易于使用,并且只需要很少的输入数据,但它给出了相当好的结果(DVWK 1996)。每天使用simmetsberg站点附近的Mittenwald-Buckelwiesen气象站(站号3307)的气象数据来运行该模型。对于该站,德国气象局(DWD)提供1937-2022年的质量控制开放数据(https://opendata.dwd.de)。为了表示可能的水平衡范围,选择生长季节(5 - 10月)最温暖(2003年)、最干燥(1947年)、最寒冷(1974年)和最潮湿(1966年)的年份进行分析。图2显示了模拟的水张力曲线和Oh层的特征值。所有测量样本的值列在表1中。总孔隙体积(TPV)在80.5% ~ 89.9%之间,空气容量(AC)在17.4% ~ 30.2%之间。FC为56.3% ~ 71.9%,PAWC为40.6% ~ 59.8%。在西梅茨堡的地点,所有相关的坦吉胡穆斯视界都可以取样。腐殖质化程度从Of到Oh再到Ovh,测量值没有明显的变化趋势。视界内(以Oh测量)和地点之间的偏差通常大于腐殖化造成的差异。因此,表1中给出的平均值可以很好地估计整个Tangelhumus剖面的持水能力。与具有最高PAWC的粉土相比,Tangelhumus层的TPV几乎是粉土的两倍,PAWC是粉土的两倍多,AC也要高得多。只有沼泽泥炭层的值高于Tangelhumus(表1)。然而,Lange Au的Ovh-horizon的测量值与报道的凸起泥炭的值非常接近。在高山地区典型的强降水事件期间,非常高的储水能力可能导致水停滞,特别是在Ovh-horizon。这种效应很可能在向底层母物质过渡时被额外的毛细管屏障所强化。由此导致的暂时缺氧,加上相当低的温度,导致分解条件受损,因此可能是坦格胡姆斯层的重要稳定因素。利用表1中每个站点的平均值和每个站点的平均坦格胡姆斯厚度,可以估计植物有效水分的储存能力(表2)。这些高值确保了林分的良好供水和在强降雨期间的高储存能力。然而,气候变化,气温上升、湿润期减少和持续高氮输入,促进了矿化,从而导致Tangelhumus逐渐退化(Gangkofner and Göttlein 2014)。腐殖质的退化减少了以腐殖质为主的森林立地的可用生根空间,降低了它们的持水能力,在极端情况下,甚至损害了它们的森林生存能力。用一个简单的模型(图3)估算基于腐殖质层厚度的水分收支,揭示了一些有趣的方面。当腐殖层的植物有效水分不能满足林分的蒸散发时,该模型计算蒸腾亏缺。在最温暖最干燥的年份和最寒冷最潮湿的年份,蒸腾亏缺的计算曲线非常接近。图3中给出的箭头表示腐殖质厚度,在此厚度以下,模型计算林分连续7天或更长时间的水分亏缺。由于Tangelhumus的高PAWC,再加上巴伐利亚阿尔卑斯山在寒冷潮湿的年份降雨量大,6厘米的腐殖质足以为林分提供水分。在温暖干燥的年份,至少需要17厘米。从长期来看,这意味着腐殖质厚度低于17厘米的林分容易受到干旱的影响,而且腐殖质层越薄,森林存活的机会就越低。我们在Allgäu、Werdenfelser Land、Mangfallgebirge和Berchtesgadener Alpen地区的24个有森林的Tangelhumus地点、云杉林和混交林测量了腐殖质厚度,总共测量了344次,这一阈值约为17厘米,得到了一项未发表的研究数据的支持。只有12和16厘米两个测量值低于上述阈值。然而,在退化森林中发现的值较低。图3还显示了根据腐殖质厚度估算的渗漏量。在凉爽和潮湿的年份,渗漏几乎保持不变,直到腐殖质厚度约为6厘米,因为蒸散发的水分损失很快被降水补偿,腐殖质层大部分时间保持饱和。 在温暖干燥的年份,渗漏量从50 cm逐渐增加到6 cm,因为腐殖质的储存能力没有得到充分利用,因此渗漏量依赖于腐殖质的厚度。在6厘米以下,随着腐殖质厚度减少到0厘米,渗漏量急剧增加,因为最终不再有任何腐殖质来储存水分或植被通过蒸发蒸腾利用水分。将腐殖质岩石转化为裸露的岩石导致每次降雨事件的快速和几乎定量的渗透。在17厘米的腐殖质处,山林在干旱年份也能勉强存活下来,而在一个完全退化的地点(0厘米的腐殖质),在所有四个模拟年份中,渗透量急剧增加,超过500毫米。作为比较,该值约为w<s:1> rzburg(1971-2000)年总降水量:583 mm;Wurzburg-Heidingsfeld;开放数据DWD)。如图1所示,生长在Tangelhumus上的森林比例在5% ~ 19%之间,Allgäu最小,Berchtesgadener Alpen最高。因此,Tangelhumus上森林的活力对于景观中的保水非常重要。如果这些森林受到诸如风、树皮甲虫或由于气候变暖而导致的坦格鲁姆退化等灾害的威胁,它们对雪崩和落石的保护功能至少可以部分地通过雪崩屏障或落石围栏等技术措施加以补偿。然而,目前还没有可行的技术替代它们的保水作用。
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来源期刊
CiteScore
4.70
自引率
8.00%
发文量
90
审稿时长
8-16 weeks
期刊介绍: Established in 1922, the Journal of Plant Nutrition and Soil Science (JPNSS) is an international peer-reviewed journal devoted to cover the entire spectrum of plant nutrition and soil science from different scale units, e.g. agroecosystem to natural systems. With its wide scope and focus on soil-plant interactions, JPNSS is one of the leading journals on this topic. Articles in JPNSS include reviews, high-standard original papers, and short communications and represent challenging research of international significance. The Journal of Plant Nutrition and Soil Science is one of the world’s oldest journals. You can trust in a peer-reviewed journal that has been established in the plant and soil science community for almost 100 years. Journal of Plant Nutrition and Soil Science (ISSN 1436-8730) is published in six volumes per year, by the German Societies of Plant Nutrition (DGP) and Soil Science (DBG). Furthermore, the Journal of Plant Nutrition and Soil Science (JPNSS) is a Cooperating Journal of the International Union of Soil Science (IUSS). The journal is produced by Wiley-VCH. Topical Divisions of the Journal of Plant Nutrition and Soil Science that are receiving increasing attention are: JPNSS – Topical Divisions Special timely focus in interdisciplinarity: - sustainability & critical zone science. Soil-Plant Interactions: - rhizosphere science & soil ecology - pollutant cycling & plant-soil protection - land use & climate change. Soil Science: - soil chemistry & soil physics - soil biology & biogeochemistry - soil genesis & mineralogy. Plant Nutrition: - plant nutritional physiology - nutrient dynamics & soil fertility - ecophysiological aspects of plant nutrition.
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