Ecological benefits of the alley cropping agroforestry system in sensitive regions of Europe

Alley cropping is an agroforestry system that offers a promising land use alternative for the temperate zone. On the same field, the sustainable production of food and biomass is possible, while simultaneously, especially in marginal areas, the ecological function of the landscape can be improved. Thus, alley cropping corresponds with the increasing demand for renewable energy resources and for a specific adaptation to the predicted changes of climatic conditions within Central Europe.However, presently, little knowledge exists regarding the effects of alley cropping on the environment. In this study a literature survey was undertaken to provide an overview of the different ecological benefits arising from alley cropping systems within temperate Europe. Abiotic factors (nutrient cycle, microclimate), biotic factors (biodiversity) and the effects on the carbon cycle are discussed in detail.Summarising, the results showed that alley cropping may be an ecologically advantageous land use system for sustainable food and biomass production in comparison with conventional agricultural practices. As a very flexible, but low-input system, alley cropping can supply biomass resources in a sustainable way and at the same time provide ecological benefits.     

Biomolecules preserved in ca. 168 million year old fossil conifer wood

Biomarkers are widely known to occur in the fossil record, but the unaltered biomolecules are rarely reported from sediments older than Paleogene. Polar terpenoids, the natural products most resistant to degradation processes, were reported mainly from the Tertiary conifers, and the oldest known are Cretaceous in age. In this paper, we report the occurrence of relatively high concentrations of ferruginol derivatives and other polar diterpenoids, as well as their diagenetic products, in a conifer wood Protopodocarpoxylon from the Middle Jurassic of Poland. Thus, the natural product terpenoids reported in this paper are definitely the oldest polar biomolecules detected in geological samples. The extracted phenolic abietanes like ferruginol and its derivatives (6,7-dehydroferruginol, sugiol, 11,14-dioxopisiferic acid) are produced only by distinct conifer families (Cupressaceae s. l., Podocarpaceae and Araucariaceae), to which Protopodocarpoxylon could belong based on anatomical characteristics. Therefore, the natural product terpenoids are of great advantage in systematics of fossil plant remains older than Paleogene and lacking suitable anatomical preservation.     

Polycyclic aromatic hydrocarbons in coastal sediments of Southern Terengganu,South China Sea,Malaysia: source assessment using diagnostic ratios and multivariate statistic

Environmental Science and Pollution Research - Surface sediments along the Southern Terengganu coast (≤7 km from the coast) were analyzed for polycyclic aromatic hydrocarbons (PAHs). The...     

Variations in the elemental compositions of plants,and computer‐aided sampling in ecosystems∗

To obtain comparable results of multi‐element analysis of plant materials by different laboratories, a harmonized sampling procedure for terrestrial and marine ecosystems is essential. The heterogeneous distribution of chemical elements in living organisms is influenced by different biological parameters. These parameters are mainly characterized by genetic predetermination, seasonal changes, edaphic and climatic conditions, and delocalization processes of chemical substances by metabolic activities.

The biological variations of the element content in plants were divided into 5 systematic levels, which are: 1. the plant species; 2. the population; 3. the stand (within an ecosystem); 4. the individual; and 5. the plant compartment. Each of these systematic levels can be related to: 1. genetic variabilities; 2. different climatic, edaphic and anthropogenic influences; 3. microclimatic or microedaphic conditions; 4. age of plants (stage of development), exposure to environmental influences (light, wind, pollution etc.), seasonal changes; and 5. transport and deposition of substances within the different plant compartments (organs, tissues, cells, organelles).

An expert system for random and systematic sampling for multi‐element analysis of environmental materials, such as plants, soils and precipitation is presented. After statistical division of the research area, the program provides advice for contamination‐free collection of environmental samples.     

塔里木河下游生态输水过程中荒漠河岸林活力恢复监测

根据近5年来对塔里木河下游荒漠河岸林植被的监测数据,分析了生态输水后植物活力的恢复状况.结果显示:应急生态输水增加了塔里木河下游的生物多样性,使原本面临死亡的荒漠河岸植被重新复活,而且不同程度上促进了胡杨群落的自然更新;在近河道50 m的范围内均出现了少量的胡杨、柽柳实生苗,并且在离河道150 m的范围内已经有相当数量的胡杨次生苗,在离河道400 m范围内大约有25%的胡杨均有不同程度的基部新枝萌蘖.通过生态输水后地下水位的逐步抬升,河道两岸的低阶地发育着一定面积的草甸植被,形成了由胡杨、柽柳和草本植物所组成的干旱区非地带性河岸稀疏植被群落,说明应急生态输水对于胡杨为建群种的荒漠河岸林植被的恢复和自然更新产生了积极的影响.     

Moosmonitoring als Spiegel der Landnutzung?

Goal, Scope and Background

The study was conducted to test the hypothesis that the regional variability of nitrogen (N) and metal accumulations in terrestrial ecosystems are due to historical and recent ways of land use. To this end, in two regions of Central Europe the metal and N accumulations in both regions should be examined by comparative moss analysis. The regions should be of quantitatively specified representativity for selected ecological characteristics of Europe. Within both regions these characteristics should be covered by the sites where the moss samples were collected. The number of samples should allow for geostatistical estimation of the measured nitrogen and metal loads.

Methods

The two regions of investigation were selected according to an ecological land classification of Europe which was computed by classification trees. Within each of both research areas the sampling points were localized according to the areas occupied by the ecologically defined land classes. The sampling and chemical analysis of mosses was conducted in accordance with an appropriate UNECE guideline by means of ICP-MS (metals) and combustion analysis (N). The quality of measurements was assured using certified reference materials. The differences of deposition loads were tested for statistical significance with regard to time and space. Variogram analysis was used to examine and model the spatial autocorrelation function of the measurements. Ordinary kriging was then applied for surface estimations.

Results

By use of the ecological regionalisation of Europe the Weser-Ems Region (WER) and the Euro Region Nissa (ERN) were selected for investigation. The sampling sites represent quite well the natural landscapes and the land use categories of both regions. The measurement values corroborate the decline of metal accumulation observed since the beginning of the European Mosses Monitoring Survey in 1990. The metal loads of the mosses in the ERN exceed those in the WER significantly. The opposite holds true for the N concentrations: those in the WER are significantly higher than those in the ERN.

Discussion

The decrease of heavy metal emissions is correlated with lowered deposition and accumulation rates in terrestrial ecosystems. The accumulation of nitrogen in the biosphere is not following this trend.

Conclusions

The technique of moss analysis is adequate for spatially valid biomonitoring of spatial and temporal trends of metals and nitrogen in terrestrial ecosystems. By this, it enables to prove the efficiency of environmental policies.

Recommendations and Perspectives

The accumulation of N in ecosystems is still a serious environmental problem. Related ecological impacts are the eutrophication of aquatic ecosystems like ground waters, lakes, rivers and oceans as well as the biocoenotic changes in terrestrial ecosystems. Thus, a statistically valid exposure analysis must encompass both, accumulation of metals and N bioaccumulation. Further, the bioaccumulation of persistent organic pollutants should be monitored. Finally, environmental biomonitoring should be conducted in much closer contact with human health aspects.     

Immunotoxic effects of environmental toxicants in fish �� how to assess them?

Numerous environmental chemicals, both long-known toxicants such as persistent organic pollutants as well as emerging contaminants such as pharmaceuticals, are known to modulate immune parameters of wildlife species, what can have adverse consequences for the fitness of individuals including their capability to resist pathogen infections. Despite frequent field observations of impaired immunocompetence and increased disease incidence in contaminant-exposed wildlife populations, the potential relevance of immunotoxic effects for the ecological impact of chemicals is rarely considered in ecotoxicological risk assessment. A limiting factor in the assessment of immunotoxic effects might be the complexity of the immune system what makes it difficult (1) to select appropriate exposure and effect parameters out of the many immune parameters which could be measured, and (2) to evaluate the significance of the selected parameters for the overall fitness and immunocompetence of the organism. Here, we present - on the example of teleost fishes - a brief discussion of how to assess chemical impact on the immune system using parameters at different levels of complexity and integration: immune mediators, humoral immune effectors, cellular immune defenses, macroscopical and microscopical responses of lymphoid tissues and organs, and host resistance to pathogens. Importantly, adverse effects of chemicals on immunocompetence may be detectable only after immune system activation, e.g., after pathogen challenge, but not in the resting immune system of non-infected fish. Current limitations to further development and implementation of immunotoxicity assays and parameters in ecotoxicological risk assessment are not primarily due to technological constraints, but are related from insufficient knowledge of (1) possible modes of action in the immune system, (2) the importance of intra- and inter-species immune system variability for the response against chemical stressors, and (3) deficits in conceptual and mechanistic assessment of combination effects of chemicals and pathogens.     

Metals in biomass

Background, Aim and Scope

Metal ions generally share the ability/tendency of interacting with biological material by forming complexes, except possibly for the heavy alkali metals K, Rb and Cs. This is unrelated to the metals being either essential for sustaining life and its reproduction, apparently insignificant for biology, although perhaps undergoing bioconcentration or even being outright toxic, even at low admission levels. Yet, those different kinds of metal-biomass interactions should in some way depend on properties describing coordination chemistries of these very metals. Nevertheless, both ubiquitously essential metals and others sometimes used in biology should share these properties in numeric terms, since it can be anticipated that they will be distinguished from nonessential and/or toxic ones. These features noted above include bioconcentration, the involvement of metal ions such as Zn, Mg, Cu, Fe, etc. in biocatalysis as crucial components of metalloenzymes and the introduction of a certain set of essential metals common to (almost) all living beings (K, Mg, Mo, Mn, Fe, Cu and Zn), which occurred probably very early in biological evolution by ‘natural selection of the chemical elements’ (more exactly speaking, of the metallomes).

Materials and Methods

The approach is semiempirical and consists of three consecutive steps: 1) derivation of a regression equation which links complex stability data of different complexes containing the same metal ion to electrochemical data pertinent to the (replaced) ligands, thus describing properties of metal ions in complexes, 2) a graphical representation of the properties-two typical numbers c and x for each metal ion-in some map across the c/x-space, which additionally contains information about biological functions of these metal ions, i.e. whether they are essential in general (e.g. Mg, Mn, Zn) or, for a few organisms of various kinds (e.g. Cd, V), not essential (e.g. rare earth element ions) or even generally highly toxic (Hg, U). It is hypothesized that, if coordination properties of metals control their biological ‘feasibility’ in some way, this should show up in the mappings (one each for mono and bidentate-bonding ligands). 3) eventually, the regression equation produced in step 1) is inverted to calculate complex stabilities pertinent to biological systems: 3a) complex stabilities are mapped for ligands delivered to soil (-water) by green plants (e.g. citrate, malate) and fungi and, compared to their unlike selectivities and demands of metal use (photosynthesis taking place or not), 3b) the evolution of the metallome during late chemical evolution is reconstructed.

Results

These maps show some ‘window of essentiality’, a small, contrived range/area of c and x parameters in which essential metal ions gather almost exclusively. c and x thus control the possibility of a metal ion becoming essential by their influencing details of metal-substrate or (in cases of catalytic activities) metal-product interactions. Exceptions are not known to be involved in biocatalysis anyhow.

Discussion

Effects of ligands secreted, e.g. from tree roots or agaric mycelia to the soil on the respective modes (selectivities) of metal bioconcentration can be calculated by the equation giving complex stability constants, with obvious ramifications for a thorough, systematic interpretation of biomonitoring data. Eventually, alterations of C, N and P-compounds during chemical evolution are investigated — which converted CH₄ or CO₂, N₂ and other non-ligands to amino acids, etc., for example, with the latter behaving as efficient chelating ligands: Did they cause metal ions to accumulate in what was going to become biological matter and was there a selectivity, a positive bias in favour of nowessential metals (see above) in this process? Though there was no complete selectivity of this kind, neither a RNA world in which early ribozymes effected most of biocatalysis, nor a paleoatmosphere containing substantial amounts of CO could have paved the way to the present biochemistry and metallomes.

Conclusions

This way of reasoning provides a causal account for abundance distributions described earlier in the Biological System of Elements (BSE; Markert 1994, Fränzle &; Markert 2000, 2002). There is a pronounced change from chemical evolution, where but few transformations depended on metal ion catalysis to biology.

Recommendations and Perspectives

The application of this numerical approach can be used for modified, weighted evaluation of biomonitoring analytical data, likewise for the prediction of bioconcentration hazards due to a manifold of metal ions, including organometallic ones. This is relevant in ecotoxicology and biomonitoring. In combining apoproteins or peptides synthesized from scratch for purposes of catalysing certain transformations, the map and numerical approaches might prove useful for the selection of central ions which are even more efficient than the ‘natural’ ones, like for Co²⁺ in many Zn enzymes.