What is soil organic matter worth?

The conservation and restoration of soil organic matter are often advocated because of the generally beneficial effects on soil attributes for plant growth and crop production. More recently, organic matter has become important as a terrestrial sink and store for C and N. We have attempted to derive a monetary value of soil organic matter for crop production and storage functions in three contrasting New Zealand soil orders (Gley, Melanic, and Granular Soils). Soil chemical and physical characteristics of real-life examples of three pairs of matched soils with low organic matter contents (after long-term continuous cropping for vegetables or maize) or high organic matter content (continuous pasture) were used as input data for a pasture (grass-clover) production model. The differences in pasture dry matter yields (non-irrigated) were calculated for three climate scenarios (wet, dry, and average years) and the yields converted to an equivalent weight and financial value of milk solids. We also estimated the hypothetical value of the C and N sequestered during the recovery phase of the low organic matter content soils assuming trading with C and N credits. For all three soil orders, and for the three climate scenarios, pasture dry matter yields were decreased in the soils with lower organic matter contents. The extra organic matter in the high C soils was estimated to be worth NZ$27 to NZ$150 ha(-1) yr(-1) in terms of increased milk solids production. The decreased yields from the previously cropped soils were predicted to persist for 36 to 125 yr, but with declining effect as organic matter gradually recovered, giving an accumulated loss in pastoral production worth around NZ$518 to NZ$1239 ha(-1). This was 42 to 73 times lower than the hypothetical value of the organic matter as a sequestering agent for C and N, which varied between NZ$22,963 to NZ$90,849 depending on the soil, region, discount rates, and values used for carbon and nitrogen credits.     

Soil quality in New Zealand: policy and the science response

Soil depletion and degradation have been increasingly recognized as important environmental issues in many parts of the world. Over the last decade a number of political and legislative measures have been introduced to encourage and enforce sustainable soil management in New Zealand. Application of the new legislation has highlighted gaps in our knowledge of soil quality and a lack of scientific methods to assess and monitor soil quality. This paper describes the legislative measures and outlines the sdentific response to the needs of regulatory agencies responsible for maintaining environmental quality. The research recommended a set of indicators to assess soil quality. Each soil quality attribute has an associated "target range" defining the acceptable value for the attribute. The paper also discusses the communication of results to end-users, including the development of a computerized assessment tool. The legislative measures and scientific response have fostered a closer relationship between the policy and science communities, leading to more well-focused research, but greater collaboration is still required.     

Relationships between ambient geochemistry, watershed land-use and trace metal concentrations in aquatic invertebrates living in stormwater treatment ponds

Stormwater treatment ponds receive elevated levels of metals from urban runoff, but the effects of these pollutants on organisms residing in the ponds are unknown. We investigated the accumulation of Cu, Zn, and Pb by macroinvertebrates collected from stormwater treatment ponds in Maryland serving commercial, highway, residential and open-space watersheds, and determined whether watershed land-use classification influences metal concentrations in macroinvertebrates, sediments, and water. Three types of invertebrate samples were analyzed--molluscs, odonates, and composite. Zn concentrations in odonates from ponds draining watersheds with commercial development (mean = 113.82 micrograms g-1) were significantly higher than concentrations in the other land-use categories. Similarly, Cu levels in odonates from commercial ponds (mean = 27.12 micrograms g-1) were significantly higher than from highway (mean = 20.23 micrograms g-1) and open space (mean = 17.79 micrograms g-1) ponds. However, metal concentrations in sediments and water did not differ significantly among land-uses. The results suggest that despite the high variation in ambient metal concentrations within each land-use category, macroinvertebrates in ponds serving commercial watersheds accumulate higher levels of Cu and Zn. The levels of Cu, Zn, and Pb in invertebrates from all ponds were less than dietary concentrations considered toxic to fish.     

Comparative toxicity of chlorpyrifos, diazinon, malathion and their oxon derivatives to larval Rana boylii

Organophosphorus pesticides (OPs) are ubiquitous in the environment and are highly toxic to amphibians. They deactivate cholinesterase, resulting in neurological dysfunction. Most chemicals in this group require oxidative desulfuration to achieve their greatest cholinesterase-inhibiting potencies. Oxon derivatives are formed within liver cells but also by bacterial decay of parental pesticides. This study examines the toxicity of chlorpyrifos, malathion and diazinon and their oxons on the foothill yellow-legged frog (Rana boylii). R. boylii is exposed to agricultural pesticides in the California Central Valley. Median lethal concentrations of the parental forms during a 96 h exposure were 3.00 mg/L (24h) for chlorpyrifos, 2.14 mg/L for malathion and 7.49 mg/L for diazinon. Corresponding oxons were 10 to 100 times more toxic than their parental forms. We conclude that environmental concentrations of these pesticides can be harmful to R. boylii populations.     

VFA generation from waste activated sludge: effect of temperature and mixing

The success of enhanced biological phosphorus removal (EBPR) depends on the constant availability of volatile fatty acids (VFAs). To reduce costs, waste streams would be a preferred source. Since VFAs were shown to vary in the incoming sewage and fermentate from primary sludge the next available source is waste activated sludge (WAS). The opportunity is particularly good in plants where WAS is stored before shipment. Little information is however available on the rate of VFA release from such sludge, especially at the lower temperatures and under the storage conditions typically found in colder climates. Bench-scale batch tests were performed to investigate the effect of temperature and requirement for mixing on VFA generation from WAS generated in full scale non-EBPR wastewater treatment plant. WAS fermentation was found highly temperature-dependent. Hydrolysis rate constant (k_h) values of 0.17, 0.08 and 0.04 d⁻¹ at 24.6, 14 and 4 °C were obtained, respectively. Arrhenius temperature coefficient was calculated to be 1.07. It took 5 d to complete hydrolysis at 24.6 °C, 7 d at 14 °C, and 9 d at 4 °C. The fermentation lasted for 20 d. At 24.6 °C the mixed reactor reached 84% of the overall VFA production only in 5 d. When temperature dropped to 14 and 4 °C, the ratio of VFA production at day 10 to overall VFA production in the mixed reactor were 62% and 48%, respectively. The overall VFA-COD concentration in the non-mixed reactors was much lower than the mixed reactors. The information is important for the designer as there was uncertainty with the effect of temperature and mixing on sludge fermentation.     

ECONOMIC EVALUATION OF ON-FARM WATER MANAGEMENT PROJECTS1

ABSTRACT: During the last three decades, developing countries have invested enormous amounts of resources (running into billions of dollars) in the development of large surface irrigation systems. Investment funds were largely spent on the development of the main systems such as dams, canals and distributaries. Very little attention and resources have been spent on the development of below-the-outlet subsystems, in spite of very low levels of water use efficiency due to lack of proper land leveling, high water losses in field channels, and skewed distribution of available water among farmers served by individual water courses. This state of affairs has resulted in a lack of confidence on the part of most farmers in the reliability of surface irrigation systems to deliver water on time and in adequate quantities which, in turn, has resulted in farmers using below optimum levels of all other complementary inputs except labor. Realizing the importance of improving water use efficiency, both the domestic governments and donor agencies are increasingly paying serious attention to these problems. On-Farm Water Management (OFWM) as a strategy to improve water use efficiency and consequently agricultural production in many developing countries has been currently receiving very wide and vigorous consideration among economists, water management experts, policymakers, and donor agencies. A judicious use of the newly allocated funds of OFWM projects obviously needs proper evaluation procedures so that money could be allocated for the most deserving purposes and projects. In particular, recently, private profitability calculations due to public investments in OFWM activities have received attention from economists and decision makers in developing countries’governments and in donor agencies are very much interested in knowing the impacts of their investments in OFWM activities on farmers’income and welfare. However, the evaluation procedures commonly used in empirical studies, using a production function approach, seem to be at variance and sometimes inconsistent with proper comparative-static procedures. Thus, the primary objective of this paper is to develop consistent procedures for evaluating the impacts created by OFWM investments on farmers’income and resource use. In this context, the paper examines the critical relationship between the market price of the agricultural output and production function parameters which are affected by the OFWM investments.     

Hydrogen gas production in a microbial electrolysis cell by electrohydrogenesis

Electrohydrogenesis is a bio-electrochemical process where organic material is microbially oxidized to protons and electrons, which in turn are reduced to form hydrogen gas (H₂). The reactor in which these reactions occur is termed a microbial electrolysis cell (MEC). The microorganisms that colonize the anode are known as electricigens and behave as biological catalysts, significantly reducing the energy required to drive this process. Electricigens are capable of complete substrate degradation, leading to very high cathodic H₂ recovery efficiencies from sources previously considered organic waste. In this short review, the origination of the bio-electrochemical system (BES) is introduced, mechanisms for electron transfer between microbe and electrode are discussed, the challenges these electrochemical systems face are presented, and finally an overview of current MEC systems and their respective performance is evaluated. Electrohydrogenesis has established itself as a promising technology for sustainable H₂ production from renewable sources.     

Metal concentrations of tadpoles in experimental ponds

Anuran tadpoles are found in a variety of habitats, many of which are acidified or have high ambient concentrations of metals from anthropogenic sources. A few studies that have been conducted on metals in tadpoles demonstrate that they can contain high concentrations of some metals but have not demonstrated clear relationships between ambient conditions and metal concentrations. This study examines the influence of soil, water treatment, amphibian species, and body portion analyzed on metal concentration in tadpoles. In northern cricket frogs, gray treefrogs, and green frogs, concentrations of Al and Fe exceeded 10 000 microg.g(-1) and Mg and Mn exceeded 1000 microg g(-1). Body concentrations of Ba, Be, Fe, Mg, Mn, Ni, Pb, and Sr increased with soil concentrations. Acidification reduced body concentrations of Be and Sr, and pH correlated with Be, Mg, and Sr. Gray treefrogs had significantly lower concentrations of most metals compared to northern cricket frogs, possibly because of differences in microhabitats and soil ingestion. More than half of most metals was sequestered in the gut coil of green frog tadpoles, probably mixed with soil. Depending on bioavailablity, many of the metals in gut coils and whole bodies of these tadpoles could be potentially toxic to predators.     

Leachate treatment before injection into a bioreactor landfill: Clogging potential reduction and benefits of using methanogenesis

In this study, an anaerobic sequencing batch reactor (ASBR) was operated with leachate from Brady Road Municipal Landfill in Winnipeg, Manitoba, Canada. Leachate was collected twice from the same cell at the landfill, during the first and 70th day of the study, and then fed into the ASBR. The ASBR was seeded at the start-up with biosolids from the anaerobic digester from Winnipeg’s North End Water Pollution Control Center (NEWPCC). Due to the higher COD and VFA removal rates measured with the second batch of leachate, an increase of approximately 0.3 pH units was observed during each cycle (from pH 7.2 to 7.5). In addition, CO₂ was produced between cycles at constant temperature where a fraction of the CO₂ became dissolved, shifting the CO₂/bicarbonate/carbonate equilibrium. Concurrent with the increase in pH and carbonate, an accumulation of fixed suspend solids (FSS) was observed within the ASBR, indicating a buildup of inorganic material over time. From it, Ca²⁺ and Mg²⁺ were measured within the reactor on day 140, indicating that most of the dissolved Ca²⁺ was removed within cycles. There is precedence from past researches of clogging in leachate-collection systems (Rowe et al., 2004) that changes in pH and carbonate content combined with high concentrations of metals such as Ca²⁺ and Mg²⁺ result in carbonate mineral precipitants. A parallel study investigated this observation, indicating that leachate with high concentration of Ca²⁺ under CO₂ saturation conditions can precipitate out CaCO₃ at the pH values obtained between digestion cycles. These studies presented show that methanogenesis of leachate impacts the removal of organic (COD, VFA) as well as inorganic (FSS, Ca²⁺) clog constituents from the leachate, that otherwise will accumulate inside of the recirculation pipe in bioreactor landfills. In addition, a robust methanogenesis of leachate was achieved, averaging rates of 0.35 L CH₄ produced/g COD removed which is similar to the theoretical removal of 0.4 L CH₄/g COD. Therefore, using methanogenesis of leachate prior to recirculation in bioreactor landfills will help to (1) control clog formation within leachate pipes and (2) produce an important additional source of energy on-site.