Larval development of the carrion-breeding flesh fly, Sarcophaga (Liosarcophaga) tibialis Macquart (Diptera: Sarcophagidae), at constant temperatures
- Villet, Martin H, MacKenzie, Bernard L, Muller, Nikite W J
- Authors: Villet, Martin H , MacKenzie, Bernard L , Muller, Nikite W J
- Date: 2006
- Language: English
- Type: text , Article
- Identifier: vital:7091 , http://hdl.handle.net/10962/d1012422
- Description: Larvae of Sarcophaga (Liosarcophaga) tibialis Macquart were raised on chicken liver under six different constant temperatures. Maximum survival indicated an optimal developmental temperature of near 20°C, while trends in mortality, larval length and larval mass implied that the thermal window for successful development lay between 15°C and 30°C. Using a recently described method to estimate a simple thermal summation model, it was found that the timing of the end of the feeding phase could be estimated by a developmental zero (D0) of 5.2°C (S.E. = 1.21) and a thermal summation constant (K) of 106.4 d°C (S.E. = 8.31) and of the end of the wandering phase by D0 = 4.1°C (S.E. = 0.39) and K = 126.7 d°C (S.E. = 3.28). Published development times at constant temperatures were compiled for 19 other species of flesh flies, and the developmental constants were calculated for six species for which sufficient data were accumulated.
- Full Text:
- Authors: Villet, Martin H , MacKenzie, Bernard L , Muller, Nikite W J
- Date: 2006
- Language: English
- Type: text , Article
- Identifier: vital:7091 , http://hdl.handle.net/10962/d1012422
- Description: Larvae of Sarcophaga (Liosarcophaga) tibialis Macquart were raised on chicken liver under six different constant temperatures. Maximum survival indicated an optimal developmental temperature of near 20°C, while trends in mortality, larval length and larval mass implied that the thermal window for successful development lay between 15°C and 30°C. Using a recently described method to estimate a simple thermal summation model, it was found that the timing of the end of the feeding phase could be estimated by a developmental zero (D0) of 5.2°C (S.E. = 1.21) and a thermal summation constant (K) of 106.4 d°C (S.E. = 8.31) and of the end of the wandering phase by D0 = 4.1°C (S.E. = 0.39) and K = 126.7 d°C (S.E. = 3.28). Published development times at constant temperatures were compiled for 19 other species of flesh flies, and the developmental constants were calculated for six species for which sufficient data were accumulated.
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The six-legged flying squad
- Villet, Martin H, Muller, Nikite W J
- Authors: Villet, Martin H , Muller, Nikite W J
- Date: 2006
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/442677 , vital:74020 , https://journals.co.za/doi/pdf/10.10520/AJA1729830X_227
- Description: How do bugs and insects help forensic entomologists to settle disputes and solve crimes? Martin Villet and Nikite Muller explain.
- Full Text:
- Authors: Villet, Martin H , Muller, Nikite W J
- Date: 2006
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/442677 , vital:74020 , https://journals.co.za/doi/pdf/10.10520/AJA1729830X_227
- Description: How do bugs and insects help forensic entomologists to settle disputes and solve crimes? Martin Villet and Nikite Muller explain.
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Similarities and differences between rivers of the Kruger National Park
- Muller, Nikite W J, Villet, Martin H
- Authors: Muller, Nikite W J , Villet, Martin H
- Date: 2004
- Language: English
- Type: text
- Identifier: vital:537 , http://hdl.handle.net/10962/d1009527
- Description: [From Introduction] Aquatic ecosystems play an important role in the maintenance of ecological diversity and ecosystem functioning at both local and regional scales (Roux et al, 1999). Effective management of riverine ecosystems requires an understanding of their ecosystem processes, hi order to understand ecosystem processes, and interactions between the landscape and riverine ecosystems, it is necessary to have both spatial and temporal data at both landscape and site-specific scales (Allan and Johnson, 1997). There are many tools available for the analysis of these data to provide insight and understanding of the data in order to understand influences on aquatic ecosystems. Increasingly complex computational tools allow analysis and modeling of data in order to explain river, and subsequent biological, processes from landscape (catchment) processes (Johnson and Gage, 1997), although the scale at which analysis and interpretation occurs is important. Science and management need to interact in order to truly succeed in effectively applying adaptive management and incorporate monitoring and assessment programmes in management processes (Rogers and Biggs, 1999). However, water resource management is often undertaken in the context of incomplete information and knowledge of functioning ecosystem processess and responses: this inevitably leads to uncertainty and unpredictability (Roux et al. 1999). One of the major challenges for managing rivers is to be able to monitor rivers effectively in order to detect changes as they occur, to identify the causes of the changes and to distinguish between natural and anthropogenic causes of change. Adaptive management is required to effectively manage rivers, but this does require that there is an understanding of, and information for, the rivers being managed. Rogers and Biggs (1999) highlighted the need to integrate monitoring programmes with indicators in order to undertake assessments of ecosystem health as part of the management plan of the rivers of the Kruger National Park in order to maintain, and restore, natural river ecosystem health and biodiversity (Rogers and Bestbier, 1997). One of the main aims of the Kruger National Park Rivers Research Programme (KNPRRP) was to contribute to the conservation of the natural environment by developing skills and methods to understand the ecological functioning of the natural environment and to predict responses of the river systems to natural and anthropogenic changes in order to effectively manage them (Breen, 1994, in van Rensburg and Dent, 1997). Classification systems are able to provide useful management information, but many have focussed on abiotic rather than biotic factors because resultant biotic patterns are likely to be correlated with abiotic components (Solomon et al., 1999). Much of the classification of the Kruger National Park has focussed on classification of land with little regard for rivers (these were incorporated into the two classification systems proposed by Venter and Gertenbach (in Solomon et al., 1999)). The objective of this project is to identify similarities and differences between the five major rivers of the Kruger National Park, towards the design and testing of a classification framework in order to aid management of the KNP rivers by contributing to effective monitoring. This will be achieved through the following: 1. collate available (current and historical) information concerning physical and biological variables for the Luvuvhu, Letaba, Olifants, Sabie and Crocodile Rivers, using a common dataset to establish the degree of similarities and differences between these five major rivers of the KNP; and 2. determine how different the rivers are, in order to optimize monitoring and management programmes for these differences. The aim of this project was not to classify the rivers of the KNP. The project rather aims to identify gaps in data availability which may result in inadequate and inappropriate management of the rivers. Results (in the form of a data matrix) emanating from this study could assist in establishing expected natural conditions and biota in the five major rivers of the KNP, and knowledge from data-rich rivers (e.g. Sabie River) could potentially be extrapolated to data-poor rivers, or sections of rivers. Invertebrates and fish are the main tools of aquatic species biodiversity monitoring, and require an understanding of the natural presence, absence and abundance patterns in aquatic ecosystems. This study contributes to this understanding by organising available information of biotic and abiotic information.
- Full Text:
- Authors: Muller, Nikite W J , Villet, Martin H
- Date: 2004
- Language: English
- Type: text
- Identifier: vital:537 , http://hdl.handle.net/10962/d1009527
- Description: [From Introduction] Aquatic ecosystems play an important role in the maintenance of ecological diversity and ecosystem functioning at both local and regional scales (Roux et al, 1999). Effective management of riverine ecosystems requires an understanding of their ecosystem processes, hi order to understand ecosystem processes, and interactions between the landscape and riverine ecosystems, it is necessary to have both spatial and temporal data at both landscape and site-specific scales (Allan and Johnson, 1997). There are many tools available for the analysis of these data to provide insight and understanding of the data in order to understand influences on aquatic ecosystems. Increasingly complex computational tools allow analysis and modeling of data in order to explain river, and subsequent biological, processes from landscape (catchment) processes (Johnson and Gage, 1997), although the scale at which analysis and interpretation occurs is important. Science and management need to interact in order to truly succeed in effectively applying adaptive management and incorporate monitoring and assessment programmes in management processes (Rogers and Biggs, 1999). However, water resource management is often undertaken in the context of incomplete information and knowledge of functioning ecosystem processess and responses: this inevitably leads to uncertainty and unpredictability (Roux et al. 1999). One of the major challenges for managing rivers is to be able to monitor rivers effectively in order to detect changes as they occur, to identify the causes of the changes and to distinguish between natural and anthropogenic causes of change. Adaptive management is required to effectively manage rivers, but this does require that there is an understanding of, and information for, the rivers being managed. Rogers and Biggs (1999) highlighted the need to integrate monitoring programmes with indicators in order to undertake assessments of ecosystem health as part of the management plan of the rivers of the Kruger National Park in order to maintain, and restore, natural river ecosystem health and biodiversity (Rogers and Bestbier, 1997). One of the main aims of the Kruger National Park Rivers Research Programme (KNPRRP) was to contribute to the conservation of the natural environment by developing skills and methods to understand the ecological functioning of the natural environment and to predict responses of the river systems to natural and anthropogenic changes in order to effectively manage them (Breen, 1994, in van Rensburg and Dent, 1997). Classification systems are able to provide useful management information, but many have focussed on abiotic rather than biotic factors because resultant biotic patterns are likely to be correlated with abiotic components (Solomon et al., 1999). Much of the classification of the Kruger National Park has focussed on classification of land with little regard for rivers (these were incorporated into the two classification systems proposed by Venter and Gertenbach (in Solomon et al., 1999)). The objective of this project is to identify similarities and differences between the five major rivers of the Kruger National Park, towards the design and testing of a classification framework in order to aid management of the KNP rivers by contributing to effective monitoring. This will be achieved through the following: 1. collate available (current and historical) information concerning physical and biological variables for the Luvuvhu, Letaba, Olifants, Sabie and Crocodile Rivers, using a common dataset to establish the degree of similarities and differences between these five major rivers of the KNP; and 2. determine how different the rivers are, in order to optimize monitoring and management programmes for these differences. The aim of this project was not to classify the rivers of the KNP. The project rather aims to identify gaps in data availability which may result in inadequate and inappropriate management of the rivers. Results (in the form of a data matrix) emanating from this study could assist in establishing expected natural conditions and biota in the five major rivers of the KNP, and knowledge from data-rich rivers (e.g. Sabie River) could potentially be extrapolated to data-poor rivers, or sections of rivers. Invertebrates and fish are the main tools of aquatic species biodiversity monitoring, and require an understanding of the natural presence, absence and abundance patterns in aquatic ecosystems. This study contributes to this understanding by organising available information of biotic and abiotic information.
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Preliminary observations on the effects of hydrocortisone and sodium methohexital on development of Sarcophaga (Curranea) tibialis Macquart (Diptera: Sarcophagidae), and implications for estimating post mortem interval
- Musvasva, E, Williams, Kirstin A, Muller, Nikite W J, Villet, Martin H
- Authors: Musvasva, E , Williams, Kirstin A , Muller, Nikite W J , Villet, Martin H
- Date: 2001
- Language: English
- Type: text , Article
- Identifier: vital:7075 , http://hdl.handle.net/10962/d1009532
- Description: Larvae of Sarcophaga (Curranea) tibialis (S. tibialis) were reared at constant temperature on chicken liver treated with a steroid or a barbiturate at concentrations that would be lethal, half-lethal and twice-lethal doses for humans. Trends to greater mortality at higher drug concentrations were not statistically significant. Larvae exposed to either drug took significantly longer to reach pupation compared to those in the control, while larvae exposed to sodium methohexital passed through pupation significantly faster than those in the control. No systematic relationship was found between drug concentration and development time of larvae or pupae. The total developmental period from hatching to eclosion did not differ between treatments, implying that estimates of post mortem intervals- (PMI) based on the emergence of adult flies will not be affected by the involvement of these drugs in a case. On the other hand, anomalous pupation spans may indicate the presence of barbiturates. These findings are compared with patterns found in another fly fed other contaminants.
- Full Text:
- Authors: Musvasva, E , Williams, Kirstin A , Muller, Nikite W J , Villet, Martin H
- Date: 2001
- Language: English
- Type: text , Article
- Identifier: vital:7075 , http://hdl.handle.net/10962/d1009532
- Description: Larvae of Sarcophaga (Curranea) tibialis (S. tibialis) were reared at constant temperature on chicken liver treated with a steroid or a barbiturate at concentrations that would be lethal, half-lethal and twice-lethal doses for humans. Trends to greater mortality at higher drug concentrations were not statistically significant. Larvae exposed to either drug took significantly longer to reach pupation compared to those in the control, while larvae exposed to sodium methohexital passed through pupation significantly faster than those in the control. No systematic relationship was found between drug concentration and development time of larvae or pupae. The total developmental period from hatching to eclosion did not differ between treatments, implying that estimates of post mortem intervals- (PMI) based on the emergence of adult flies will not be affected by the involvement of these drugs in a case. On the other hand, anomalous pupation spans may indicate the presence of barbiturates. These findings are compared with patterns found in another fly fed other contaminants.
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