Dörte Diehl

Review on environmental alterations propagating from aquatic to terrestrial ecosystems.

Terrestrial inputs into freshwater ecosystems are a classical field of environmental science. Resource fluxes (subsidy) from aquatic to terrestrial systems have been less studied, although they are of high ecological relevance particularly for the receiving ecosystem. These fluxes may, however, be impacted by anthropogenically driven alterations modifying structure and functioning of aquatic ecosystems. In this context, we reviewed the peer-reviewed literature for studies addressing the subsidy of terrestrial by aquatic ecosystems with special emphasis on the role that anthropogenic alterations play in this water-land coupling. Our analysis revealed a continuously increasing interest in the coupling of aquatic to terrestrial ecosystems between 1990 and 2014 (total: 661 studies), while the research domains focusing on abiotic (502 studies) and biotic (159 studies) processes are strongly separated. Approximately 35% (abiotic) and 25% (biotic) of the studies focused on the propagation of anthropogenic alterations from the aquatic to the terrestrial system. Among these studies, hydromorphological and hydrological alterations were predominantly assessed, whereas water pollution and invasive species were less frequently investigated. Less than 5% of these studies considered indirect effects in the terrestrial system e.g. via food web responses, as a result of anthropogenic alterations in aquatic ecosystems. Nonetheless, these very few publications indicate far-reaching consequences in the receiving terrestrial ecosystem. For example, bottom-up mediated responses via soil quality can cascade over plant communities up to the level of herbivorous arthropods, while top-down mediated responses via predatory spiders can cascade down to herbivorous arthropods and even plants. Overall, the current state of knowledge calls for an integrated assessment on how these interactions within terrestrial ecosystems are affected by propagation of aquatic ecosystem alterations. To fill these gaps, we propose a scientific framework, which considers abiotic and biotic aspects based on an interdisciplinary approach.

Influence of biochar and terra preta substrates on wettability and erodibility of soils

Biochar (BC) and terra preta substrates (TPS) have recently been promoted as soil amendments suitable for soil stabilization, soil amelioration and long-term carbon sequestration. BC is a carbon-enriched substance produced by thermal decomposition of organic material. TPS is composed of liquid and solid organic matter, including BC, altered by acid-lactic fermentation. Their effect on wettability, soil erodibility and nutrient discharge through overland flow was studied by laboratory experiments. At water contents between 0 and 100% BC is water repellent, while TPS changes from a wettable into a repellent state. The 5 and 10 vol % mixtures of BC and 10 and 20 vol% mixtures of TPS with sand remain mainly wettable during drying but repellency maxima are shifted to higher water contents with respect to pure sand and are mainly of subcritical nature. The runoff response was dominated by infiltration properties of the substrates rather than their wettability.Only one mixtures (20% TPS) produced more runoff than sandy-loamy soil on a 15% slope at an intensity of 25 mm•h-1. The 10% BC decreased runoff by up to 40%. At higher rainfall intensities (45 and 55 mm•h-1) the 10% TPS7 was up to 35% less erodible than 10% BC. Despite the TPS containing more nutrients, nutrient discharge varied between types of nutrients, slopes, rainfall intensities and mixtures. The application of a 1 cm layer onto the soil surface instead of 10% mixtures is not recommended due to high nutrient concentrations in the runoff and the wettability of pure substrates. The usage of 10% BC in lowland areas with low frequency and low-intensity precipitation and 10% TPS7 in areas with higher rainfall intensities appears to be appropriate and commendable according to current results. However, together with reversibility of repellency, it needs to undergo further examination in the field under different environmental and land use conditions

Restructuring of a Peat in Interaction with Multivalent Cations: Effect of Cation Type and Aging Time

It is assumed to be common knowledge that multivalent cations cross-link soil organic matter (SOM) molecules via cation bridges (CaB). The concept has not been explicitly demonstrated in solid SOM by targeted experiments, yet. Therefore, the requirements for and characteristics of CaB remain unidentified. In this study, a combined experimental and molecular modeling approach was adopted to investigate the interaction of cations on a peat OM from physicochemical perspective. Before treatment with salt solutions of Al3+, Ca2+ or Na+, respectively, the original exchangeable cations were removed using cation exchange resin. Cation treatment was conducted at two different values of pH prior to adjusting pH to 4.1. Cation sorption is slower (>>2 h) than deprotonation of functional groups (<2 h) and was described by a Langmuir model. The maximum uptake increased with pH of cation addition and decreased with increasing cation valency. Sorption coefficients were similar for all cations and at both pH. This contradicts the general expectations for electrostatic interactions, suggesting that not only the interaction chemistry but also spatial distribution of functional groups in OM determines binding of cations in this peat. The reaction of contact angle, matrix rigidity due to water molecule bridges (WaMB) and molecular mobility of water (NMR analysis) suggested that cross-linking via CaB has low relevance in this peat. This unexpected finding is probably due to the low cation exchange capacity, resulting in low abundance of charged functionalities. Molecular modeling demonstrates that large average distances between functionalities (∼3 nm in this peat) cannot be bridged by CaB-WaMB associations. However, aging strongly increased matrix rigidity, suggesting successive increase of WaMB size to connect functionalities and thus increasing degree of cross-linking by CaB-WaMB associations. Results thus demonstrated that the physicochemical structure of OM is decisive for CaB and aging-induced structural reorganisation can enhance cross-link formation.

Effect of multivalent cations, temperature and aging on soil organic matter interfacial properties

Environmental context The supramolecular structure and resulting physicochemical properties of soil organic matter (SOM) significantly control storage and buffer functions of soils, e.g. for nutrients, organic molecules and water. Multivalent cations, able to form complexes, are suggested to form inter- and intramolecular cross-links in SOM. At present, specific effects of the valence and type of cation on SOM properties are incompletely understood. We investigated changes in SOM interfacial properties, its ability to release mobile colloids in aqueous solutions and its sorption affinity towards organic chemicals in dependence on cation–SOM interactions, temperature and aging time. Abstract The present study aims to improve our understanding on the effect of multivalent cations, temperature treatment and isothermal aging time on interfacial soil organic matter (SOM) properties as major factors that modify its supramolecular structures. A sandy topsoil (LW) and a peat soil (SP) were enriched with Na, Ca or Al, or desalinated in a batch experiment, treated at 25, 40, 60 and 105°C and aged at constant temperature and humidity (20°C, 31% relative humidity). After aging for different periods, contact angles (CAs), sorption properties towards xenobiotics and properties of water dispersible colloids were determined. With increasing valence of the dominant cations fewer and larger colloids were observed, probably attributable to cation cross-links or enhanced aggregation caused by reduced surface charge. Al-enrichment of LW resulted in more abundant or more accessible sorption sites for hydrophobic xenobiotics. But in contrast to expectations, hydrophilic sorption as well as wettability was not significantly affected by the type of adsorbed cation. Increasing the temperature had a major effect on surface properties resulting in rising surface hydrophobisation with increasing solid–water CAs, decreasing surface O/C ratio and decreasing sorption of hydrophilic substances; whereas systematic temperature effects on water dispersible colloids and on hydrophobic sorption were not detected. Aging was found to increase the initial CA of the 25°C treatment and to increase the sorption of phenanthrene to LW for all treatment temperatures. We conclude that aging of SOM is a process that changes surface properties and approaches a new equilibrium state after a disturbance. The aging process may be significantly accelerated for samples treated at elevated temperatures.

Effects of olive mill wastewater disposal on soil: Interaction mechanisms during different seasons

Abstract Environmental conditions play a major role for effects of olive mill wastewater (OMW) application to soil. Choosing a different season for OMW application than the commonly practiced winter, may help avoid negative effects. However, understanding of the OMW-soil interaction during different seasons is still incomplete due to the lack of comparative data. In this study, an 18 months field experiment was carried out in an olive orchard in West Bank. Degree and persistence of soil salinization, acidification, accumulation of phenolic compounds and soil water repellency were investigated as a function of soil depth and time elapsed after OMW application, which was performed either in spring, summer (with and without irrigation) or winter. The persistence of negative effects increased with duration of the hot and dry period following the application due to accumulation and polymerization of OMW. On the other hand, leaching of OMW components to groundwater is favored during the rainy season and by formation of preferential flow paths before the rain season starts. The risks of groundwater contamination and persistent negative effects decrease with increasing time under conditions favoring biological activity. Therefore, OMW application in spring if improved by a careful irrigation is considered as the most suitable under semiarid conditions for clay loam soils.

The effect of pH modification on wetting kinetics of a naturally water-repellent coniferous forest soil

The interfacial dynamics of soil–water interactions are greatly affected by the hydrophobic properties of organic matter. The causes and underlying mechanisms responsible for the development of soil water repellency (SWR) are still under discussion. Various environmental factors control the appearance and degree of SWR. In addition to water content and temperature, the wetting of soil depends greatly on the physicochemical characteristics of soil surfaces, which in turn depend on pH. In this contribution, we propose a reaction mechanism for the change in SWR that is observed when soil pH is changed. Wetting kinetics were studied by time-dependent sessile drop measurements (TISED) of the contact angle, the work of spreading and the diameter of the base of the drop as time elapsed under controlled relative humidity. Modification of pH strongly affected the wetting kinetics, suggesting maximum resistance to wetting at the control pH (3.6), with decreased resistance to wetting as pH was changed in either direction. The enhancement in wetting kinetics by the modification of soil pH can be attributed to the chemical modification in organic materials that coat the soil particles. This conclusion is based on the magnitude of activation energy associated with the spreading process. The combined effect of pH and temperature on the wetting kinetics, together with the compensation effect seen between the logarithmic pre-exponential factor and activation energy, suggests acid–base catalysed hydrolysis–condensation reactions are the dominant processes responsible for the chemical nature of SWR. Highlights How does the modification of pH affect soil wetting mechanisms? The dynamic sessile drop method was used to measure the wetting activation energy. Modification of soil pH decreases resistance to wetting and increases activation energy of wetting. Acid or base catalysed hydrolysis reactions increase chemical sorption sites for water molecules in soil.

Links between nanoscale and macroscale surface properties of natural root mucilage studied by atomic force microscopy and contact angle

Soil water repellency originating from organic coatings plays a crucial role for soil hydraulics and plant water uptake. Focussing on hydrophobicity in the rhizosphere induced by root-mucilage, this study aims to explore the link between macroscopic wettability and nano-microscopic surface properties. The existing knowledge of the nanostructures of organic soil compounds and its effect on wettability is limited by the lack of a method capable to assess the natural spatial heterogeneity of physical and chemical properties. In this contribution, this task is tackled by a geostatistical approach via variogram analysis of topography and adhesion force data acquired by atomic force microscopy and macroscopic sessile drop measurements on dried films of mucilage. The results are discussed following the wetting models given by Wenzel and Cassie-Baxter. Undiluted mucilage formed homogeneous films on the substrate with contact angles >90°. For diluted samples contact angles were smaller and incomplete mucilage surface coverage with hole-like structures frequently exhibited increased adhesion forces. Break-free distances of force curves indicated enhanced capillary forces due to adsorbed water films at atmospheric RH (35 ± 2%) that promote wettability. Variogram analysis enabled a description of complex surface structures exceeding the capability of comparative visual inspection.