10 research outputs found
Venom toxicity and deployment method as means of biotic resistance
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Allozyme and Other Aspects of Variation in the Genus Bulbinella in New Zealand
This thesis examines some aspects of morphological, cytogenetic and allozyme variation in the six species of the genus Bulbinella in New Zealand. Because evidence was found suggesting that fragmentation and reduction of the habitat of some species of the study genus had occurred, aspects of the conservation status of Bulbinella were also investigated. Some of the morphological characters described and used by Moore (1964) to separate the species were employed in this study as well as other characters recorded by the author in actively glowing plants. Generally, the seven taxa could be successfully distinguished using selected morphological characters, although in some species or populations a range of morphological forms was observed. Increased human land use (mainly mining, farming and associated activities) has reduced some populations of Bulbinella to low numbers by destroying large areas of habitat. In some cases once vast areas of Bulbinella have been reduced to fragments or probably exterminated. The karyotypes of five of the seven taxa were determined and these were all consistent with published data. G-banding was achieved in only one slide from one plant. A total of four bands (restricted to two pairs of chromosomes) was observed in the entire chromosome complement of 14. Each band was located on a separate chromosome. Inflorescence material from 61 natural populations of Bulbinella in New Zealand was examined for enzyme activity using starch gel electrophoresis. Activity was detected for eight of a total of 43 enzyme stains. Three monomorphic and 11 polymorphic loci were resolved. While no completely fixed differences between all the taxa could be demonstrated, four almost fixed differences were found. In some instances where populations belonging to different species were not geographically separated by great distances (<50km) shared alleles between species were demonstrated, indicating that introgression had occurred and may still be taking place. Overall, the genetic distance (Nei 1978) within taxa was less than that between taxa. The dendrogram resulting from cluster analysis of Nei's unbiased genetic distances divided the genus into four groups, three of which corresponded to three currently recognised taxa. The other group contained the remaining four taxa. Although the component taxa of this cluster could be readily separated using morphological characters, they could not be distinguished using allozyme data. The endemic distribution of B. rossii (Campbell Island and Auckland Island Group) and fixed morphological differences justify its remaining a separate taxon. The formal raising of B. gibbsii var. gibbsii to a separate specific status is subject to the analysis of further samples of this taxon. B. angustifolia, B, talbotii, and B. gibbsii vat. balanifera also remain separate taxa, with B. gibbsii var. balanifera being raised to a separate specific status. B. modesta, which is genetically closely related to B. hookeri, becomes a sub-species of this taxon
Allozyme and Other Aspects of Variation in the Genus Bulbinella in New Zealand
This thesis examines some aspects of morphological, cytogenetic and allozyme variation in the six species of the genus Bulbinella in New Zealand. Because evidence was found suggesting that fragmentation and reduction of the habitat of some species of the study genus had occurred, aspects of the conservation status of Bulbinella were also investigated. Some of the morphological characters described and used by Moore (1964) to separate the species were employed in this study as well as other characters recorded by the author in actively glowing plants. Generally, the seven taxa could be successfully distinguished using selected morphological characters, although in some species or populations a range of morphological forms was observed. Increased human land use (mainly mining, farming and associated activities) has reduced some populations of Bulbinella to low numbers by destroying large areas of habitat. In some cases once vast areas of Bulbinella have been reduced to fragments or probably exterminated. The karyotypes of five of the seven taxa were determined and these were all consistent with published data. G-banding was achieved in only one slide from one plant. A total of four bands (restricted to two pairs of chromosomes) was observed in the entire chromosome complement of 14. Each band was located on a separate chromosome. Inflorescence material from 61 natural populations of Bulbinella in New Zealand was examined for enzyme activity using starch gel electrophoresis. Activity was detected for eight of a total of 43 enzyme stains. Three monomorphic and 11 polymorphic loci were resolved. While no completely fixed differences between all the taxa could be demonstrated, four almost fixed differences were found. In some instances where populations belonging to different species were not geographically separated by great distances (<50km) shared alleles between species were demonstrated, indicating that introgression had occurred and may still be taking place. Overall, the genetic distance (Nei 1978) within taxa was less than that between taxa. The dendrogram resulting from cluster analysis of Nei's unbiased genetic distances divided the genus into four groups, three of which corresponded to three currently recognised taxa. The other group contained the remaining four taxa. Although the component taxa of this cluster could be readily separated using morphological characters, they could not be distinguished using allozyme data. The endemic distribution of B. rossii (Campbell Island and Auckland Island Group) and fixed morphological differences justify its remaining a separate taxon. The formal raising of B. gibbsii var. gibbsii to a separate specific status is subject to the analysis of further samples of this taxon. B. angustifolia, B, talbotii, and B. gibbsii vat. balanifera also remain separate taxa, with B. gibbsii var. balanifera being raised to a separate specific status. B. modesta, which is genetically closely related to B. hookeri, becomes a sub-species of this taxon
Allozyme and Other Aspects of Variation in the Genus Bulbinella in New Zealand
This thesis examines some aspects of morphological, cytogenetic and allozyme variation in the six species of the genus Bulbinella in New Zealand. Because evidence was found suggesting that fragmentation and reduction of the habitat of some species of the study genus had occurred, aspects of the conservation status of Bulbinella were also investigated. Some of the morphological characters described and used by Moore (1964) to separate the species were employed in this study as well as other characters recorded by the author in actively glowing plants. Generally, the seven taxa could be successfully distinguished using selected morphological characters, although in some species or populations a range of morphological forms was observed. Increased human land use (mainly mining, farming and associated activities) has reduced some populations of Bulbinella to low numbers by destroying large areas of habitat. In some cases once vast areas of Bulbinella have been reduced to fragments or probably exterminated. The karyotypes of five of the seven taxa were determined and these were all consistent with published data. G-banding was achieved in only one slide from one plant. A total of four bands (restricted to two pairs of chromosomes) was observed in the entire chromosome complement of 14. Each band was located on a separate chromosome. Inflorescence material from 61 natural populations of Bulbinella in New Zealand was examined for enzyme activity using starch gel electrophoresis. Activity was detected for eight of a total of 43 enzyme stains. Three monomorphic and 11 polymorphic loci were resolved. While no completely fixed differences between all the taxa could be demonstrated, four almost fixed differences were found. In some instances where populations belonging to different species were not geographically separated by great distances (<50km) shared alleles between species were demonstrated, indicating that introgression had occurred and may still be taking place. Overall, the genetic distance (Nei 1978) within taxa was less than that between taxa. The dendrogram resulting from cluster analysis of Nei's unbiased genetic distances divided the genus into four groups, three of which corresponded to three currently recognised taxa. The other group contained the remaining four taxa. Although the component taxa of this cluster could be readily separated using morphological characters, they could not be distinguished using allozyme data. The endemic distribution of B. rossii (Campbell Island and Auckland Island Group) and fixed morphological differences justify its remaining a separate taxon. The formal raising of B. gibbsii var. gibbsii to a separate specific status is subject to the analysis of further samples of this taxon. B. angustifolia, B, talbotii, and B. gibbsii vat. balanifera also remain separate taxa, with B. gibbsii var. balanifera being raised to a separate specific status. B. modesta, which is genetically closely related to B. hookeri, becomes a sub-species of this taxon.</p
Arena fight and venom usage
The table "Arena fight and venom usage.csv" corresponds to the manuscript sections of the same name. It contains the mortality of Argentine ant and workers of four Monomorium ant species after 1, 4 and 24 hours, as well as behavioural responses and observed venom usage of ant workers in the arena trials. It furthermore contains data derived from this raw data (for example relative occurence of behaviours). The experimental design is explained in the publication in the methods section with the same name as the datafile, further description of this and the other datafiles associated with this publication can be found in the ReadMe.tx
Data from: Toxicity and utilization of chemical weapons: does toxicity and venom utilization contribute to the formation of species communities?
Toxicity and the utilization of venom are essential features in the ecology of many animal species and have been hypothesized to be important factors contributing to the assembly of communities through competitive interactions. Ants of the genus Monomorium utilize a variety of venom compositions, which have been reported to give them a competitive advantage. Here, we investigate two pairs of Monomorium species, which differ in the structural compositions of their venom and their co-occurrence patterns with the invasive Argentine ant. We looked at the effects of Monomorium venom toxicity, venom utilization, and aggressive physical interactions on Monomorium and Argentine ant survival rates during arena trials. The venom toxicity of the two species co-occurring with the invasive Argentine ants was found to be significantly higher than the toxicity of the two species which do not. There was no correlation between venom toxicity and Monomorium survival; however, three of the four Monomorium species displayed significant variability in their venom usage which was associated with the number of Argentine ant workers encountered during trials. Average Monomorium mortality varied significantly between species, and in Monomorium smithii and Monomorium antipodum, aggressive interactions with Argentine ants had a significant negative effect on their mortality. Our study demonstrates that different factors and strategies can contribute to the ability of a species to withstand the pressure of a dominant invader at high abundance, and venom chemistry appears to be only one of several strategies utilized
Venom survivability
The table "Venom survivability.csv" corresponds to the manuscript sections of the same name. It contains the responses of Argentine ants after 1 and 4 hours when treated with different concentrations of venom of four different Monomorium ant species and can be used to calculate the LD 50 of these venoms on Argentine ants. The experimental design is explained in the publication in the methods section with the same name as the datafile, further description of this and the other datafiles associated with this publication can be found in the ReadMe.tx
Arena fight and venom usage Monomorium Survival
The table "Arena fight and venom usage Monomorium Survival.csv" corresponds to the manuscript section "Arena fight and venom usage". It contains data represented in the Monomorium Mortality column in table "Arena fight and venom usage.csv" formatted for a survival analysis. The experimental design is explained in the publication in the methods section with the same name as the datafile, further description of this and the other datafiles associated with this publication can be found in the ReadMe.tx
Arena fight and venom usage Argentine ant Survival
The table "Arena fight and venom usage Argentine ant Survival.csv" corresponds to the manuscript section "Arena fight and venom usage". It contains data represented in the Argentine ant Mortality column in table "Arena fight and venom usage.csv" formatted for a survival analysis. The experimental design is explained in the publication in the methods section with the same name as the datafile, further description of this and the other datafiles associated with this publication can be found in the ReadMe.tx