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Van Sickle, J.

Publications and source records attributed to Van Sickle, J..

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Improved models for the relationship between age and the probability of trypanosome infection in female tsetse, Glossina pallidipes Austen

Between 1990 and 1999, at Rekomitjie Research Station, Zambezi Valley, Zimbabwe, 29,360 female G. pallidipes were dissected to determine their ovarian category and trypanosome infection status. Overall prevalences were 3.45% and 2.66% for T. vivax and T. congolense, respectively, declining during each year as temperatures increased from July - December. Fits to age-prevalence data using Susceptible-Exposed-Infective (SEI) and SI compartmental models were statistically better than those obtained using a published catalytic model, which made the unrealistic assumption that no female tsetse survived more than seven ovulations. The improved models require knowledge of fly mortality, estimated separately from ovarian age distributions. Infection rates were not significantly higher for T. vivax than for T. congolense. For T. congolense in field-sampled female G. pallidipes, we found no statistical support for a model where the force of infection was higher at the first feed than subsequently. The long survival of adult female tsetse, combined with feeding at intervals [≤] 3 days, ensures that post-teneral feeds, rather than the first feed, play the dominant role in the epidemiology of T. congolense infections in G. pallidipes. This is supported by estimates that only about 3% of wild hosts at Rekomitjie were harbouring sufficient T. congolense to ensure that tsetse feeding off them take an infected meal, so that the probability of ingesting an infected meal is low at every meal.

zoology↗

Apparent negative density-dependent dispersal in tsetse (Glossina spp) is an artefact of inappropriate analysis

Analysis of genetic material from field-collected tsetse (Glossina spp) in ten study areas has been used to predict that the distance ({delta}) dispersed per generation increases as effective population densities (De) decrease, displaying negative density dependent dispersal (NDDD). This result is an artefact arising primarily from errors in estimates of S, the area occupied by a subpopulation, and thereby in De, the effective subpopulation density. The fundamental, dangerously misleading, error lies in the assumption that S can be estimated as the area ([S]) regarded as being covered by traps. Errors in the estimates of{delta} are magnified because variation in estimates of S is greater than for all other variables measured, and accounts for the greatest proportion of variation in{delta} . The errors result in anomalously high correlations between{delta} and S, and the appearance of NDDD, with a slope of -0.5 for the regressions of log({delta}) on log(e), even in simulations where dispersal has been set as density independent. A complementary mathematical analysis confirms these findings. Improved error estimates for the crucial parameter b, the rate of increase in genetic distance with increasing geographic separation, suggest that three of the study areas should have been excluded because b is not significantly greater than zero. Errors in census population estimates result from a fundamental misunderstanding of the relationship between trap placement and expected tsetse catch. These errors are exacerbated through failure to adjust for variations in trapping intensity, trap performance, and in capture probabilities between geographical situations and between tsetse species. Claims of support in the literature for NDDD are spurious. There is no suggested explanation for how NDDD might have evolved. We reject the NDDD hypothesis and caution that the idea should not be allowed to influence policy on tsetse and trypanosomiasis control. Author summaryGenetic analysis of field-sampled tsetse (Glossina spp) has been used to suggest that, as tsetse population densities decrease, rates of dispersal increase - displaying negative density dependent dispersal (NDDD). It is further suggested that NDDD might apply to all tsetse species and that, consequently, tsetse control operations might unleash enhanced invasion of areas cleared of tsetse, prejudicing the long-term success of control campaigns. We demonstrate that NDDD in tsetse is an artefact consequent on multiple errors of analysis and interpretation. The most serious of these errors stems from a fundamental misunderstanding of the way in which traps sample tsetse, resulting in huge errors in estimates of the areas sampled by the traps, and occupied by the subpopulations being sampled. Errors in census population estimates are made worse through failure to adjust for variations in trapping intensity, trap performance, and in capture probabilities between geographical situations, and between tsetse species. The errors result in the appearance of NDDD, even in modelling situations where rates of dispersal are expressly assumed independent of population density. We reject the NDDD hypothesis and caution that the idea should not be allowed to influence policy on tsetse and trypanosomiasis control.

zoology↗