29 research outputs found

    Thermocline management of stratified tanks for heat storage

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    Stratified tanks are useful for maximising the thermal energy efficiency of non-continuous and semi-continuous processes. Liquid at two or more dissimilar temperatures is stored within the same tank to provide a buffer for variations in heating and cooling loads. Control of the thermocline between the hot and cold fluid regions is needed to minimise thermocline growth and maximise operation of the storage tank. An experimental programme using a scale model of an industrial stratified tank (aspect ratio 3.5) and Perspex tank (aspect ratio 8.2) is reported. The behaviour and growth of the hot-cold thermocline under various operating conditions is presented. A siphoning method to re-establish the thermocline without interrupting the use of the tank is tested. Siphoning of the thermocline region from either 20%, 50% or 80% of the tank height is an effective strategy for uninterrupted interface re-establishment. However, the rate and position of siphoning and the load balance of the exit streams are critical variables for minimising the time for effective re-establishment of the two temperature zones

    Submaximal Oviposition Rates in a Mymarid Parasitoid: Choosiness Should Not Be Ignored

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    Cronin and Strong (1993a, b) examined the oviposition behavior of Anagarus delicatus Dozier (Hymenoptera: Mymaridae), an egg parasitoid of the leafhopper Prokelisia marginate Van Duzee (Homoptera: Delphacidae). They reported oviposition rates that were lower than predicted if the rate of egg-laying was maximized. Cronin and Strong (1993a) considered, and subsequently rejected, several “rules of thumb” (Stephens and Krebs 1986) as explanations for the observed patterns of patch departure. They observed that hosts on leaves experience density-independent mortality due to leaf senescence. Based on that, they advanced the hypothesis that submaximal oviposition rates in A. delicatus are best explained as risk-spreading by the parasitoid. (That is, by laying a small number of eggs on many leaves, the parasitoid increases the probability that some of her offspring will survive; Cronin and Strong 1993a.) An alternative hypothesis (Rosenheim and Mangel 1994) suggests that by distributing the eggs among several leaves, A. delicatus avoids self-superparasitism. Here, we take a somewhat different approach than those provided above to explain an additional observation of Cronin and Strong (1993a): female wasps rejected most of the hosts that they had probed. In so doing, we argue that rate maximization was an inappropriate prediction for A. delicatus, and in light of the life history parameters of this species, egg limitation is more suitable. Furthermore, egg limitation, when combined with one of the proposed explanations for the distribution of eggs, can explain the high rejection level of potential hosts

    Submaximal Oviposition Rates in a Mymarid Parasitoid: Choosiness Should Not Be Ignored

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    Cronin and Strong (1993a, b) examined the oviposition behavior of Anagarus delicatus Dozier (Hymenoptera: Mymaridae), an egg parasitoid of the leafhopper Prokelisia marginate Van Duzee (Homoptera: Delphacidae). They reported oviposition rates that were lower than predicted if the rate of egg-laying was maximized. Cronin and Strong (1993a) considered, and subsequently rejected, several “rules of thumb” (Stephens and Krebs 1986) as explanations for the observed patterns of patch departure. They observed that hosts on leaves experience density-independent mortality due to leaf senescence. Based on that, they advanced the hypothesis that submaximal oviposition rates in A. delicatus are best explained as risk-spreading by the parasitoid. (That is, by laying a small number of eggs on many leaves, the parasitoid increases the probability that some of her offspring will survive; Cronin and Strong 1993a.) An alternative hypothesis (Rosenheim and Mangel 1994) suggests that by distributing the eggs among several leaves, A. delicatus avoids self-superparasitism. Here, we take a somewhat different approach than those provided above to explain an additional observation of Cronin and Strong (1993a): female wasps rejected most of the hosts that they had probed. In so doing, we argue that rate maximization was an inappropriate prediction for A. delicatus, and in light of the life history parameters of this species, egg limitation is more suitable. Furthermore, egg limitation, when combined with one of the proposed explanations for the distribution of eggs, can explain the high rejection level of potential hosts

    Studies on the dispersal behaviour of apterous pea aphids acyrthosiphon pisum (Harris)

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    The dispersal behaviour of apterous pea aphids, Acyrthosipon pi sum (Harris) was studied in the laboratory and field. In the laboratory, aphids exhibited two types of behaviour while on the ground, after dropping from plants in response to predators. Most aphids showed a high frequency of turning and tended to return to the plant they left, while a smaller proportion walked in straight lines and did not return to the plant they left. Adults and older nymphs had the highest proportion of individuals which showed the second type of behaviour and adults showed the greatest tendency to disperse to plants more distant than the nearest available plants. Young instar aphids were less successful at locating a host than older nymphs and adults. Aphids were placed on the central bean seedlings within plots, inside large field cages. Adult coccinellids were released into two of the cages while the other cage remained predator-free. Aphids in the cages with predators frequently moved between plants, while aphids in the predator-free cage did not. Adult aphids colonized more plants and had a lower mortality while on the ground than all other instars. Aphids did not show a preferred dispersal direction and the distance dispersed by aphid nymphs was proportional to the density of aphids on the plant they left. The importance of emigrating apterae in the exploitation of new resources and the regulation of aphid populations is discussed. Bean plants infected with an aphid transmitted virus were transplanted into the central position of bean plots in the field cages. Aphids were placed on the central infected plants and adult coccinellids were released into two of the three cages for three days. Aphids frequently moved to other plants from the centre infected plant in the two cages with predators but not in the predator-free cage. When plants were examined two weeks later, significantly more plants were infected with virus in the cages with predators than in the predator-free cage. New virus infections were correlated with plants that were visited or colonized by aphids from the central infected plant. The influence of predators in the spread of aphid transmitted diseases is discussed. In laboratory experiments, pea aphids from Vancouver were presented with alarm pheromone from irritated conspecifics. Adult and fourth instar aphids responded to the pheromone by either dropping, running or backing up. Instars one, two and three responded to the pheromone only when a vibratory stimulus accompanied it. A high proportion of all instars responded to the double stimulus by dropping. When adult aphids from Vancouver and Kamloops were presented with alarm pheromone, the Kamloops adults exhibited a more conservative reaction to alarm pheromone. Kamloops adults also were more conservative about leaving their plant when confronted by a coccinellid predator. A hypothesis is presented, which accounts for the differences in escape reactions between instars and biotypes. The hypothesis takes into consideration predation risk, escape behaviour repertoire and survival on the ground. Pea aphid adults resisted heat paralysis longer than first instars when subjected to high temperature treatments. All aphids succumbed to paralysis sooner at 42°C than at 37.5°C, but there appeared to be no difference in aphid survival in dry compared to moist conditions at high temperatures. Kamloops aphids were not more resistant to high temperatures.Land and Food Systems, Faculty ofGraduat

    Comparative Flight Dynamics of Knapweed Gall Flies Urophora quadrifasciata and U. affinis (Diptera: Tephritidae)

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    By using laboratory flight mills, I tested the hypothesis that the differential distributions of knapweed gall flies, Urophora quadrifasciata and U. affinis, among knapweed sites can be predicted by the flight propensity and endurance of the flies. Results from tests did not support the prediction that the former species displays the greater propensity for flight and endurance. I discuss several reasons supporting the values obtained and their validity for use in interspecific comparisons. Finally, I point to the danger of extrapolating laboratory behaviour to the field

    Life-history decisions under predation risk: Importance of a game perspective

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    We model ontogenetic shifts (e.g. in food or habitat use) during development under predation risk. We ask whether inclusion of state and frequency dependence will provide new insights when compared with game-free life-history theory. We model a simple biological scenario in which a prey animal must switch from a low-predation, low-growth habitat to a high-predation, high-growth habitat. To assess the importance of frequency dependence, we compare the results of four scenarios of increasing complexity: (1) no predation; (2) constant predation; (3) frequency-dependent predation (predation risk diluted at high prey density); and (4) frequency-dependent predation as in (3) but with predators allowed to respond adaptively to prey behavior. State dependence is included in all scenarios through initial size, assumed to be environmental. A genetic algorithm is used to search for optimal solutions to the scenarios. We find substantially different results in the four different scenarios and suggest a decision tree by which biological systems could be tested to ascertain which scenario is most applicable

    Effects of body size on investment in individual broods by male pine engravers (Coleoptera: Scolytidae)

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