Zabrotes subfasciatus é considerado um dos principais predadores de sementes da espécie Phaseolus vulgaris, causando sérios prejuízos para esta espécie em armazenagem. Este trabalho teve como objetivo conhecer alguns dados do comportamento de oviposição das fêmeas de Z. subfasciatus (Coleoptera, Bruchidae) que ainda são desconhecidos. Foi estudada a oviposição de Z. subfasciatus em P. vulgaris, ao longo de toda a vida e em situações de privação do hospedeiro, logo após a emergência dos adultos, por períodos determinados de 1 a 10 dias. Foi utilizada apenas uma variedade de P. vulgaris: rosinha. O trabalho foi dividido em 2 fases, realizadas concomitantemente. Na primeira fase, foi estudada a variação da oviposição, ao longo do tempo de vida total das fêmeas, sem e com privação do hospedeiro, por até 10 dias, bem como a variabilidade entre as fêmeas dentro de cada grupo, observando as estratégias de cada uma delas no interior de cada grupo. Foram analisados vários parâmetros, como: número de ovos colocados diariamente, a longevidade, o período de oviposição e o número de ovos colocados por cada fêmea dentro de cada grupo. O número de ovos depositados por dia variou estatisticamente, sendo que o pico de oviposição na presença do hospedeiro (Grupo Controle) ocorreu entre o 2o e 5o dia de postura. A longevidade média foi de 11,1±1,8; o período de oviposição médio foi de 8,7±1,1 dias e o número de ovos colocados por cada fêmea ao longo da vida foi de 37,0±9,3. Nos Grupos em que houve privação do hospedeiro, também observou-se que o número de ovos colocados por dia foi diferente estatisticamente, sendo que o pico de oviposição ocorreu sempre no 1o. dia seguinte à privação, com exceção do nível 1, em que o pico ficou entre os dias 1 e 4 (após a presença do hospedeiro). A fecundidade máxima de cada grupo diminuiu, mas só foi diferente estatisticamente a partir do nível 6 (6 dias sem o hospedeiro), sendo que a média foi de 13,9±9,2 ovos, quando o tempo de espera foi de 10 dias. Isso sugere que em até 5 dias de privação, Z. subfasciatus consegue manter sua capacidade de postura, graças a uma boa retenção dos seus ovos e, a partir do 6o dia, há, provavelmente, uma reabsorção. A longevidade foi maior nos Grupos de Privação do hospedeiro a partir do nível 3, em relação ao Grupo Controle, mas o período de oviposição foi menor (4,3±4,6 dias no nível 10) a partir do nível 1, em relação ao Grupo Controle. O número de ovos colocados por todas as fêmeas, tanto no Grupo Controle como nos de Privação, não diferiu, indicando assim que não há variabilidade intraespecífica dentro de cada grupo. Na segunda fase, o objetivo foi comparar a distribuição dos ovos por grão, no Grupo em que não houve privação do hospedeiro (Controle) e nos Grupos em que houve privação por 2, 5, 8 e 10 dias, respectivamente. Foi constatado que as fêmeas privadas do hospedeiro por 5 e 8 dias apresentaram maior número de grãos com 4 ou mais ovos, no 1o dia de oviposição (1,4 grão em média), em relação ao Grupo Controle e as fêmeas que ficaram privadas do hospedeiro por 2 e 10 dias (0,8 grão em média). Quanto ao número de grãos com 1 ou nenhum ovo, observou-se que o Grupo Controle e os Grupos em que houve privação do hospedeiro por 8 e 10 dias apresentaram um maior número de grãos (3,2 grãos em média) em relação aos demais (2,1 grãos em média), no 1o dia de oviposição. E quanto ao número de ovos no grão com mais ovos, observou-se que ocorreu um maior número de ovos em todos os Grupos Privados (5,1 ovos/ grão em média), em relação ao Grupo Controle (1,9 ovo/ grão, em média). / Zabrotes subfasciatus is considered to be one of the main predators of Phaseolus vulgaris seeds, causing severe damage to this species during storage. The aim of the present study was to investigate some aspects of the oviposition behavior of Z. subfasciatus (Coleoptera, Bruchidae) females that are still unknown. The oviposition of Z. subfasciatus on P. vulgaris was studied along the entire life cycle of the parasite and in situations of host privation, right after the emergence of the adults, for periods of time ranging from one to ten days. Only one variety of P. vulgaris ("rosinha") was used. The study was divided into two parts carried out concomitantly. In the first part, the variation of oviposition along the total lifetime of the females was studied, with and without host privation up to ten days, as well as the variability among the females inside each group, with individual observation of the strategies of each insect. Several parameters were analyzed: number of eggs laid daily, longevity, oviposition period and number of eggs laid per female inside each group. The number of eggs laid per day varied significantly and the peak oviposition in the presence of the host (Control Group) occurred between the second and the fifth day after deposition. The mean longevity was 11.1 ± 1.8 days, the mean oviposition period was 8.7 ± 1.1 days and the number of eggs laid by each female along their lives was 37.0 ± 9.3. In the groups submitted to host privation the number of eggs deposited per day was significantly different, with peak oviposition occurring always on the first day after privation, except for level 1 where the peak was observed between the first and fourth days (after the presence of the host). The maximum fecundity of each group has reduced, but the difference was statistically significant only when level 6 (six days without the host) and higher levels were reached, the average being 13.9 ± 9.2 eggs when the waiting time was ten days. This suggests that, for up to five days of privation, Z. subfasciatus is able to maintain its oviposition capacity thanks to the good retention of its eggs. After the sixth day, however, reabsorption is likely to occur. The longevity of the groups submitted to host privation from level 3 to higher levels was longer than the longevity of the Control Group, but the oviposition period from level 1 to higher levels (4.3 ± 4.6 days at level 10) was lower than in the Control Group. The number of eggs laid by all females in the Control and Privation Groups did not differ, thus indicating that there is no intraspecific variability inside each group. In the second part of the experiment, the aim was to compare the distribution of eggs per grain in the group where there was no host privation (Control) and in the groups where privations of 2, 5, 8 and 10 days were imposed. The females kept under host privation for 5 and 8 days presented a larger number of grains with four or more eggs on the first day of oviposition (average of 1.4 grains) compared with the Control Group and with the females that were kept under host privation for 2 and 10 days (average of 0.8 grains). As regards the number of grains with one or no egg, the Control Group and the groups submitted to host privation for 2 and 10 days presented a larger number of grains (average of 3.2 grains) in relation to the others (average of 2.1 grains) on the first day of oviposition. As regards the number of eggs on the grains with a larger content of eggs, the number of eggs was larger in all the Privation Groups (average of 5.1 eggs/grain) in relation to the Control Group (average of 1.9 eggs/grain).

Wheat midge, Sitodiplosis mosellana (Géhin) (Diptera: Cecidomyiidae), is a key pest of wheat, Triticum aestivum L. (Poaceae), in the Canadian Prairies. The larvae destroy wheat kernels, resulting in reduction of quality and quantity of wheat. Deployment of antixenotic wheat lines, which suppress oviposition of wheat midge, can reduce damage in wheat fields. The objectives of this thesis were to explore the interactions between wheat midge and spring wheat with emphasis on oviposition behavior and to explore the antixenosis of wheat to oviposition from the point of view of genetics and crop breeding. In this research, a doubled-haploid spring wheat population was studied, which was the progeny of a cross between a susceptible wheat cultivar ‘Roblin’ and a resistant (antixenotic and antibiotic) wheat line ‘Key 10’. Oviposition of wheat midge on wheat spikes in the laboratory was affected by visual and chemical cues. The visual contrast between wheat spikes and the background color in the laboratory was important in modifying oviposition of wheat midge on wheat spikes. Low contrast resulted in low egg density on wheat spikes in the laboratory. The egg density on wheat spikes in the laboratory decreased when the background color of the spikes was red or black; while yellow and blue backgrounds did not decrease egg density on the spikes. The laboratory study provided evidence that wheat midge oviposition was affected by volatiles emitted by wheat spikes. The volatiles of spikes of a post-anthesis susceptible wheat cultivar, ‘Roblin’, and a pre-anthesis resistant wheat line, ‘Key 10’, significantly suppressed the oviposition of wheat midge in the laboratory. It is hypothesized that these volatiles might be a factor in antixenosis of wheat against wheat midge in the doubled-haploid population studied. It is suggested that the differences of oviposition behavior in susceptible and antixenotic wheats, which was observed in the laboratory, might be due to volatiles emitted by wheat spikes. However, other factors such as tactile cues might also be involved. The observation of oviposition behavior in the laboratory on the susceptible wheat cultivar ‘Roblin’ showed that wheat midge started ovipositing sooner, stayed longer, laid more eggs and left the spike sooner after the last oviposition than on the antixenotic line ‘Key 10’. However, the time required for laying one egg was similar when wheat midge was on the susceptible or resistant wheat. The observed antennation behavior of wheat midge while probing the wheat spike might indicate that wheat midge probed for chemical cues emitted by the host plant. The observed ovipositor tapping and dragging on the wheat spike surface while probing the spike suggested that there might be receptors at the tip of the ovipositor which receive tactile cues from the plant surface, guiding oviposition. The correlations between morphological traits of bread wheat spikes and antixenosis in the laboratory were not high enough to conclude that those traits were associated with antixenosis. However, more research on fine scale morphological traits of the spike may reveal relationships with antixenosis. Based on data from a laboratory trial and trials in the field over two field seasons, it was concluded that the antixenosis to wheat midge in the doubled-haploid population was probably conferred by two genes with complementary interactions among genes, and a heritability of 67%. In the two field seasons, the least preferred line received 13% and 11% as many eggs as on ‘Roblin’; ‘Key 10’ received 57% and 20% as may eggs as on ‘Roblin’. Our study did not provide evidence for linkage between antixenosis genes and the antibiosis gene, Sm1, which is associated with death of larvae of wheat midge. The antixenosis of spring wheat against wheat midge can be considered as a promising mechanism for suppressing wheat midge oviposition in the field. More research is required to reveal additional genetic information which would help crop breeders in production of cultivars antixenotic to wheat midge.

Wheat midge, Sitodiplosis mosellana (Géhin) (Diptera: Cecidomyiidae), is a key pest of wheat, Triticum aestivum L. (Poaceae), in the Canadian Prairies. The larvae destroy wheat kernels, resulting in reduction of quality and quantity of wheat. Deployment of antixenotic wheat lines, which suppress oviposition of wheat midge, can reduce damage in wheat fields. The objectives of this thesis were to explore the interactions between wheat midge and spring wheat with emphasis on oviposition behavior and to explore the antixenosis of wheat to oviposition from the point of view of genetics and crop breeding. In this research, a doubled-haploid spring wheat population was studied, which was the progeny of a cross between a susceptible wheat cultivar ‘Roblin’ and a resistant (antixenotic and antibiotic) wheat line ‘Key 10’. Oviposition of wheat midge on wheat spikes in the laboratory was affected by visual and chemical cues. The visual contrast between wheat spikes and the background color in the laboratory was important in modifying oviposition of wheat midge on wheat spikes. Low contrast resulted in low egg density on wheat spikes in the laboratory. The egg density on wheat spikes in the laboratory decreased when the background color of the spikes was red or black; while yellow and blue backgrounds did not decrease egg density on the spikes. The laboratory study provided evidence that wheat midge oviposition was affected by volatiles emitted by wheat spikes. The volatiles of spikes of a post-anthesis susceptible wheat cultivar, ‘Roblin’, and a pre-anthesis resistant wheat line, ‘Key 10’, significantly suppressed the oviposition of wheat midge in the laboratory. It is hypothesized that these volatiles might be a factor in antixenosis of wheat against wheat midge in the doubled-haploid population studied. It is suggested that the differences of oviposition behavior in susceptible and antixenotic wheats, which was observed in the laboratory, might be due to volatiles emitted by wheat spikes. However, other factors such as tactile cues might also be involved. The observation of oviposition behavior in the laboratory on the susceptible wheat cultivar ‘Roblin’ showed that wheat midge started ovipositing sooner, stayed longer, laid more eggs and left the spike sooner after the last oviposition than on the antixenotic line ‘Key 10’. However, the time required for laying one egg was similar when wheat midge was on the susceptible or resistant wheat. The observed antennation behavior of wheat midge while probing the wheat spike might indicate that wheat midge probed for chemical cues emitted by the host plant. The observed ovipositor tapping and dragging on the wheat spike surface while probing the spike suggested that there might be receptors at the tip of the ovipositor which receive tactile cues from the plant surface, guiding oviposition. The correlations between morphological traits of bread wheat spikes and antixenosis in the laboratory were not high enough to conclude that those traits were associated with antixenosis. However, more research on fine scale morphological traits of the spike may reveal relationships with antixenosis. Based on data from a laboratory trial and trials in the field over two field seasons, it was concluded that the antixenosis to wheat midge in the doubled-haploid population was probably conferred by two genes with complementary interactions among genes, and a heritability of 67%. In the two field seasons, the least preferred line received 13% and 11% as many eggs as on ‘Roblin’; ‘Key 10’ received 57% and 20% as may eggs as on ‘Roblin’. Our study did not provide evidence for linkage between antixenosis genes and the antibiosis gene, Sm1, which is associated with death of larvae of wheat midge. The antixenosis of spring wheat against wheat midge can be considered as a promising mechanism for suppressing wheat midge oviposition in the field. More research is required to reveal additional genetic information which would help crop breeders in production of cultivars antixenotic to wheat midge.

Zabrotes subfasciatus é considerado um dos principais predadores de sementes da espécie Phaseolus vulgaris, causando sérios prejuízos para esta espécie em armazenagem. Este trabalho teve como objetivo conhecer alguns dados do comportamento de oviposição das fêmeas de Z. subfasciatus (Coleoptera, Bruchidae) que ainda são desconhecidos. Foi estudada a oviposição de Z. subfasciatus em P. vulgaris, ao longo de toda a vida e em situações de privação do hospedeiro, logo após a emergência dos adultos, por períodos determinados de 1 a 10 dias. Foi utilizada apenas uma variedade de P. vulgaris: rosinha. O trabalho foi dividido em 2 fases, realizadas concomitantemente. Na primeira fase, foi estudada a variação da oviposição, ao longo do tempo de vida total das fêmeas, sem e com privação do hospedeiro, por até 10 dias, bem como a variabilidade entre as fêmeas dentro de cada grupo, observando as estratégias de cada uma delas no interior de cada grupo. Foram analisados vários parâmetros, como: número de ovos colocados diariamente, a longevidade, o período de oviposição e o número de ovos colocados por cada fêmea dentro de cada grupo. O número de ovos depositados por dia variou estatisticamente, sendo que o pico de oviposição na presença do hospedeiro (Grupo Controle) ocorreu entre o 2o e 5o dia de postura. A longevidade média foi de 11,1±1,8; o período de oviposição médio foi de 8,7±1,1 dias e o número de ovos colocados por cada fêmea ao longo da vida foi de 37,0±9,3. Nos Grupos em que houve privação do hospedeiro, também observou-se que o número de ovos colocados por dia foi diferente estatisticamente, sendo que o pico de oviposição ocorreu sempre no 1o. dia seguinte à privação, com exceção do nível 1, em que o pico ficou entre os dias 1 e 4 (após a presença do hospedeiro). A fecundidade máxima de cada grupo diminuiu, mas só foi diferente estatisticamente a partir do nível 6 (6 dias sem o hospedeiro), sendo que a média foi de 13,9±9,2 ovos, quando o tempo de espera foi de 10 dias. Isso sugere que em até 5 dias de privação, Z. subfasciatus consegue manter sua capacidade de postura, graças a uma boa retenção dos seus ovos e, a partir do 6o dia, há, provavelmente, uma reabsorção. A longevidade foi maior nos Grupos de Privação do hospedeiro a partir do nível 3, em relação ao Grupo Controle, mas o período de oviposição foi menor (4,3±4,6 dias no nível 10) a partir do nível 1, em relação ao Grupo Controle. O número de ovos colocados por todas as fêmeas, tanto no Grupo Controle como nos de Privação, não diferiu, indicando assim que não há variabilidade intraespecífica dentro de cada grupo. Na segunda fase, o objetivo foi comparar a distribuição dos ovos por grão, no Grupo em que não houve privação do hospedeiro (Controle) e nos Grupos em que houve privação por 2, 5, 8 e 10 dias, respectivamente. Foi constatado que as fêmeas privadas do hospedeiro por 5 e 8 dias apresentaram maior número de grãos com 4 ou mais ovos, no 1o dia de oviposição (1,4 grão em média), em relação ao Grupo Controle e as fêmeas que ficaram privadas do hospedeiro por 2 e 10 dias (0,8 grão em média). Quanto ao número de grãos com 1 ou nenhum ovo, observou-se que o Grupo Controle e os Grupos em que houve privação do hospedeiro por 8 e 10 dias apresentaram um maior número de grãos (3,2 grãos em média) em relação aos demais (2,1 grãos em média), no 1o dia de oviposição. E quanto ao número de ovos no grão com mais ovos, observou-se que ocorreu um maior número de ovos em todos os Grupos Privados (5,1 ovos/ grão em média), em relação ao Grupo Controle (1,9 ovo/ grão, em média). / Zabrotes subfasciatus is considered to be one of the main predators of Phaseolus vulgaris seeds, causing severe damage to this species during storage. The aim of the present study was to investigate some aspects of the oviposition behavior of Z. subfasciatus (Coleoptera, Bruchidae) females that are still unknown. The oviposition of Z. subfasciatus on P. vulgaris was studied along the entire life cycle of the parasite and in situations of host privation, right after the emergence of the adults, for periods of time ranging from one to ten days. Only one variety of P. vulgaris ("rosinha") was used. The study was divided into two parts carried out concomitantly. In the first part, the variation of oviposition along the total lifetime of the females was studied, with and without host privation up to ten days, as well as the variability among the females inside each group, with individual observation of the strategies of each insect. Several parameters were analyzed: number of eggs laid daily, longevity, oviposition period and number of eggs laid per female inside each group. The number of eggs laid per day varied significantly and the peak oviposition in the presence of the host (Control Group) occurred between the second and the fifth day after deposition. The mean longevity was 11.1 ± 1.8 days, the mean oviposition period was 8.7 ± 1.1 days and the number of eggs laid by each female along their lives was 37.0 ± 9.3. In the groups submitted to host privation the number of eggs deposited per day was significantly different, with peak oviposition occurring always on the first day after privation, except for level 1 where the peak was observed between the first and fourth days (after the presence of the host). The maximum fecundity of each group has reduced, but the difference was statistically significant only when level 6 (six days without the host) and higher levels were reached, the average being 13.9 ± 9.2 eggs when the waiting time was ten days. This suggests that, for up to five days of privation, Z. subfasciatus is able to maintain its oviposition capacity thanks to the good retention of its eggs. After the sixth day, however, reabsorption is likely to occur. The longevity of the groups submitted to host privation from level 3 to higher levels was longer than the longevity of the Control Group, but the oviposition period from level 1 to higher levels (4.3 ± 4.6 days at level 10) was lower than in the Control Group. The number of eggs laid by all females in the Control and Privation Groups did not differ, thus indicating that there is no intraspecific variability inside each group. In the second part of the experiment, the aim was to compare the distribution of eggs per grain in the group where there was no host privation (Control) and in the groups where privations of 2, 5, 8 and 10 days were imposed. The females kept under host privation for 5 and 8 days presented a larger number of grains with four or more eggs on the first day of oviposition (average of 1.4 grains) compared with the Control Group and with the females that were kept under host privation for 2 and 10 days (average of 0.8 grains). As regards the number of grains with one or no egg, the Control Group and the groups submitted to host privation for 2 and 10 days presented a larger number of grains (average of 3.2 grains) in relation to the others (average of 2.1 grains) on the first day of oviposition. As regards the number of eggs on the grains with a larger content of eggs, the number of eggs was larger in all the Privation Groups (average of 5.1 eggs/grain) in relation to the Control Group (average of 1.9 eggs/grain).

No description available.