The empirical modeling of an ecosystem

The authors have endeavored to create a verified a-posteriori model of a planktonic ecosystem. Verification of an empirically derived set of first-order, quadratic differential equations proved elusive due to the sensitivity of the model system to changes in initial conditions. Efforts to verify a similarly derived set of linear differential equations were more encouraging, yielding reasonable behavior for half of the ten ecosystem compartments modeled. The well-behaved species models gave indications as to the rate-controlling process in the ecosystem.     

The effects of corona electrode geometry on the operational characteristics of an ESP

Experiments were run in a pilot scale electrostatic precipitator (ESP) to determine the effects of corona wire-to-wire spacing on the operating conditions. Tests were run, using a reentrained low sulfur fly ash at both hot- and cold-side conditions. The effects of varying wire-to-wire spacing were determined. Results are given which show that varying wire spacing at cold-side conditions has little operational effect on the ESP while improved efficiency can be obtained at hot-side (low resistivity) conditions by reducing wire spacing. The increased efficiency results from a higher average operating voltage. The effects of back ionization are clearly demonstrated by a set of experiments in which dust was selectively removed from the wires or plate. These tests show that the lower operating voltage caused by back ionization is a combined effect of high resistivity dust on both the wires and plate.     

FRAGILE ESTUARINE SYSTEMS–ECOLOGICAL CONSIDERATIONS1

Studies of fish species and populations indicate a high degree of fragility for estuarine ecosystems. Slight stresses tend to disrupt energy flow systems and lead to lower levels of biological productivity, shortened food chains and poorer diversity of species. For individual species low-level stresses tend to suppress metabolism and growth processes. Minor stresses can also substantially reduce populations. Stress processes are quantifiable and amenable to mathematical modeling.     

Environmental Persistence of Chemicals

- DOI: http://dx.doi.org/10.1065/espr2006.01.008 Background The hazard criterion of persistence as it applies to chemicals in the environment is reviewed and discussed. This quantity can not be measured directly in the environment, thus it must be estimated using models that synthesise information on chemical half-lives and partitioning properties, the nature of the environment and how the chemical is released into the environment. Main Features It is suggested that the preferred criterion is the average residence time of the chemical in the environment, i.e. conceptually the sum of the life-times of all molecules (attributable only to losses by degrading reactions) divided by the number of molecules. If all chemical fate processes are first order, this persistence is independent of the quantity of chemical introduced and whether introduction is steady- or unsteady-state in nature. It is shown that in a multimedia environment persistence is affected not only by degradation kinetics, but also by mode-of-entry and partitioning. For screening level purposes a Level II equilibrium model may be adequate but a Level III model is generally preferable for estimating the average persistence. If a distribution of persistences is required a dynamic Level IV model must be used. Discussion The implications for regulating chemicals on the basis of persistence are discussed. Conclusion It is concluded that the preferred strategy is to use Level II, III, and IV models and that the use of only degradation kinetics or media-specific half-lives can be misleading and uneconomical.     

Movements and swimming behaviour of white sharks (Carcharodon carcharias) in Australian waters

We used a combination of satellite telemetry, archival and conventional tags to show that white sharks made broad-scale movements consistent with mixing of the population across their entire Australasian range. The capture of one of these sharks in New Zealand, some 3,550 km from the point of tagging in South Australia, provides further confirmation that white sharks sometimes move into open ocean waters and cross deep ocean basins. However, most movements were confined to shelf waters, generally in areas of less than 100 m depth and in some cases into waters of less than 5 m depth. Sharks showed considerable plasticity in swimming patterns, which included many of the behaviours reported for other species. One of the archival-tagged sharks showed separate periods of distinct swimming behaviour as it moved into different habitats and travelled between them. The changes in swimming behaviour were abrupt and suggested rapid switching of hunting strategies for different prey types in these habitats. All tracked sharks showed both prolonged periods of directional swimming in coastal waters at swimming speeds of 2–3 km h⁻¹ as well as temporary residency in particular regions. Movements of tagged white sharks, together with data from shark control programs and bycatch records, suggest a seasonal movement northward along the east coast of Australia during the autumn–winter months and south in spring–early summer. The consistency of paths taken by white sharks in Australian waters suggests that they may follow common routes or “highways” in some areas. If so, identifying such areas may assist in reducing interactions with fishing operations and thus reduce bycatch.     

Application of ‘Landsat’ data to resource management

Over the past few years, a great deal of interest has been focused on the use of remote sensing for resource management. This paper examines one of the most useful systems — Landsat. Included in this paper is a discussion of this remote-sensing technology, its application and its future as a tool for resources planning and management.     

The use of measurable coefficients in process formulations—zooplankton grazing

This paper redefines a construct previously used to model phytoplankton—zooplankton interactions in such a way as to permit the use of measurable quantities as contruct coefficients. The new construct can use unaltered values of the half-saturation constant for zooplankton grazing on total available food (k_s) and the minimum food concentration necessary to stimulate effective feeding (BMIN) reported in the literature. Typical values for these coefficients are 0.1–15 and 0.016–0.19, respectively.     

Foraging in the seed-harvester ant genus Pogonomyrmex: are energy costs important?

Energy intake and expenditure on natural foraging trips were estimated for the seed-harvester ants, Pogonomyrmex maricopa and P. rugosus. During seed collection, P. maricopa foraged individually, whereas P. rugosus employed a trunk-trail foraging system. Energy gain per trip and per minute were not significantly different between species. There was also no interspecific difference in energy cost per trip, but energy cost per minute was lower for P. maricopa foragers because they spent on average 7 min longer searching for a load on each trip. Including both unsuccessful and successful foraging trips, average energy gain per trip was more than 100 times the energy cost per trip for both species. Based on this result, we suggest that time cost incurred during individual foraging trips is much more important than energy cost in terms of maximizing net resource intake over time. In addition, because energy costs are so small relative to gains, we propose that energy costs associated with foraging may be safely ignored in future tests of foraging theory with seed-harvesting ant species.