Interaction of population processes in ragwort (Senecio jacobaea L.) and ragwort flea beetle (Longitarsus jacobaeae Waterhouse) : a thesis presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Ecology at Massey University

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Date
2000
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Massey University
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The primary goal of this study was to improve understanding of biological control of weeds by investigating how population processes in ragwort and herbivorous insect interact. Specific aims were to measure the consumption rates of the three larval instars of ragwort flea beetle (Longitarsus jacobaeae), to investigate how the process of herbivory by ragwort flea beetle affects the population density of ragwort, and to investigate how soil moisture influences the population densities of ragwort flea beetle and ragwort. An extraction apparatus was constructed to obtain L. jacobaeae larvae from ragwort roots and root crowns. This apparatus was 84% efficient . A preliminary survey of ragwort flea beetle numbers included ragwort plants from B allantrae, Turakina, and Pahiatua (Southern North Island, New Zealand). The larval population was highest at Ballantrae but the adul t population was highest at Turakina. Data were collected from Ballantrae from 1996 to 1998 to develop the interaction model between L. jacobaeae and ragwort. The interaction depended on the effect that soil water content had on the populations of both L. jacobaeae and ragwort, the effect that larval density has on larval mortality, and the effect of ragwort density on the population of L. jacobaeae larvae. Soil water content was positively correlated with the increase in numbers of L. jacobaeae. L. jacobaeae larval mortality was dependent on larval density. High numbers of larvae per plant resulted in a reduction in the number of larvae over time ( 1 3 .6 larvae/plant on November 1 997 to 1 .8 larvae/plant in December 1997). The average number of larvae extracted at Ballantrae was lower in October and November 1996 (4.4 and 4.6 larvae/plant) than in October and November 1 997 ( 1 3.4 and 1 3. 6 larvae/plant). However, the average numbers of rosettes was higher in October and November 1 996 (7.6 and 5 .78m -2) than in October and November 1 997 (2.8 and 2 .7 m -\ There was a significant inverse correlation between the numbers of L. jacobaeae larvae and ragwort rosettes (-0.4608). When 0.8983 in 1 5 day old larvae, 0.926 1 in 30 day old larvae, and 0.9454 in 45 day old larvae. The lowest percentage survival (0.9067 in 15 day old larvae) was found at the highest larval density (40 larvae per plant). Finally, the same experiment was tested in a field and the data from this was used to construct an interaction model for L. jacobaeae and its food, ragwort. This model was based on the correlation between soil water and populations of L. jacobaeae and ragwort; the effect of larval density on the mortality of larvae and on the weight loss o f ragwort; and on the effect that ragwort density has on the mortality of L. jacobaeae larvae. Mean soil water was 1 2 ± 0.29 to 7 6 ± l.8 1 % over the first 1 5 days, then 3 6 ± 1 . 1 0 to 8 2 ± 0.99% up to 30 days, and 35 ± 0.76 to 65 ± 1 .78% up to 45 days of larval life. These were the soil water contents that occurred during the field experiment. The model showed that the highest larval survival again occurred when few larvae were introduced to ragwort plants ( 1 7.5% survival from 0- 1 5 days, 1 4.33% from 1 6-30 days, and 1 8 .5% from 3 1 -45 days). High larval densities also produced the lowest survival (8.4% survival over 0- 15 days, 5 .87% over 1 6-30 days, and 6.7% over 3 1 -45 days). The effect of plant density on larval survival was also tested in the field. The highest larval survival (10.76%) occurred when there were on 1 6 plants m-2, and the larvae were 0 to IS -days old. The lowest larval survival (6. 6 1 %) occurred with 1 6-30 day old larvae on plants at a density of 4 plantsm-2. A cohort life-table was constructed for predicting population fluctuations of L. jacobaeae. Values from this life table were used to model populations of L. jacobaeae, ragwort and the interactions between these species using "STELLA" software. Data for the ragwort model was obtained from published papers. Additional data from the experimental determination of feeding rates of L. jacobaeae larvae were used when both the L. jacobaeae and ragwort models were combined to examine the interactions between these species. This latter model was used to estimate population fluctuations of L. jacobaeae and its food over two years. It indicated that L. jacobaeae is a very effective control agent for ragwort, and that it can cause ragwort populations to decline to extinction within two years.
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Weed control, Biological control
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