The paleoecology of plant - arthropod herbivory associations constitute very important source of knowledge about the phylogeny and co-evolution of both groups. The traces of herbivory interactions between plants and arthropods on the fossil leaves are preserved as so called damaged types (DTs) clustered into distinct functional feeding groups (FFGs). The diversity and frequency of these damage traces also seem to have been strongly influenced by environmental and climatic conditions. This research has been focused on rich fossil plant assemblages from the area of the Most Basin in the north-western Bohemia. The undergoing work has comprised the diagnosis of the individual damages on the basis of their specific morphological traits as their number, size, shape and distributional pattern on the leaf surface. The next issue has involved the statistical analyses concerning the differences in the frequency and diversity of the types of damage and functional feeding groups between two separate fossiliferous layers, namely those of the stratigraphically older Bílina Delta and younger Břešťany Clay. Significant differences were confirmed in this regard, especially in connection with achieved frequency and proportional occurrences of distinct functional feeding groups in the Bílina Delta. The galls were the...

Attempts were made to grow Fergusobia nematodes in a dual aseptic culture with Eucalyptus camaldulensis. Callus tissue was grown from E. camaldulensis stem pieces in aseptic conditions. Calli were prone to deterioration after 14 days unless transferred to fresh growth medium. Lower levels of solutes (25% Murashige and Skoog salts, 25% plant vitamins and 0.5% sucrose) were more successful than published concentrations. Fergusobia J2 nematodes were surface sterilised with either Hibitane or washed with water to prepare them for inoculation of callus (Hay, 1994). Fergusobia subsequently recovered from plates of callus were all dead, which raised questions of how the nematodes are suited to Murashige and Skoog salt solutions. The survival of Fergusobia in aqueous solutions was then observed. It has been assumed that Fergusobia live about 2 days after dissection. Amphimictic nematodes from E. camaldulensis axial bud galls were used for a survival study. Nematodes lived for as long as 12 days in fresh tap water and 11 days in 1% M.S. solution. They were more active in tap water than in 1% M.S. solution. Nematodes in a dish together with dissected gall material died within 2 days. Nematodes in a separate dish with fresh tap water and clean gall fibres were observed to gather around the fibres. Observations of Fergusobia could be made within fresh solutions providing deteriorating gall tissues were removed from the dish. Gall production was attempted on E. camaldulensis grown in the glasshouse. These tree saplings were pruned to encourage new growth and periodically treated for infestations of scale insects leading to growth of sooty mould. Two forms of cage construction were used: (1) 1 m ³ screened cages and (2) acetate sleeves as used by Goolsby et al., 2000. Within the 1 m ³ cages containing flies, the growing points on saplings were blackened, possibly due to over-exploitation by ovipositing flies. One growing point caged in an acetate sleeve showed oviposition scars but did not produce a mature gall. Production of galls in the glasshouse was hindered by a lack in coincidence of flies emerging from mature galls and the flush of new growth following pruning. The production of galls within the glasshouse was not achieved. The phenology of E. camaldulensis, a host for the Fergusonina/Fergusobia mutualism, and gall ecology were observed in a two-year, non-destructive, field study in the Urrbrae Wetlands, Adelaide, South Australia. Tree growth and gall development was observed in the lower regions (0 – 2 m) of young trees. Three bud forms, terminal leaf bud, axial leaf bud and flower bud galls were monitored on the trees. The densities of galls were highly seasonal. Greatest density of growing points, axial leaf bud and flower bud galls occurred mostly during mid-winter to spring, whereas that of terminal leaf bud galls occurred during mid-spring to summer. Galling of flower buds did not appear to influence flowering and more flower buds and flowers occurred in the second year of the study as the trees matured. Trees mostly had medium (30-70%) levels of leaf damage, but there were seasonal trends in damage levels. Low scores for leaf damage were associated with increases in flower bud and flower production. Leaf damage, including sooty mould, appeared to increase during the cooler winter months. There were no significant seasonal relationships between levels of leaf damage and either growing point density or the occurrence of galls. When trees were compared with each other, those with lower leaf damage were more likely to have more growing points. The appearance of the canopy and the likelihood of a tree to have galls varied greatly between the trees. One tree was particularly susceptible to leaf attack, rarely had new leaves and produced no mature galls during the study. The colouring of leaves varied between trees, which indicates possible genetic variations causing some trees to be more likely hosts for Fergusonina/Fergusobia. Both new vegetative growth and terminal leaf bud galls were concentrated on the northern and eastern quadrants. Axial leaf bud and flower bud galls occurred more on the western or southern quadrants where they were possibly more protected from sun exposure on the northern or eastern quadrants. Axial galls on the northern side of one tree became reddened while those in the southern and western quadrants remained green. Reddening of axial galls may increase their likelihood of parasitism and predation by birds. Each of the three gall forms occurred within certain positions in the canopy. The tree host resource is partitioned effectively, with the three gall forms occurring on three different host structures. Additionally, the two vegetative forms terminal leaf bud and axial leaf bud galls occur on different shoot regions and in different seasons. The numbers of the galls is probably also affected by biotic and climatic influences. Parasitism, plant canopy shading, nutrient levels and host genetics are possible influences. Assuming an interval of 4 weeks between oviposition and first observation within the current study, terminal leaf bud galls had an average longevity of 11 weeks and axial leaf bud galls an average longevity of 14 weeks. Flower bud galls had longevities of 14 to 27 weeks from oviposition to senescence, assuming an interval of 6 weeks between oviposition and first observation within the current study. Flowers and flower buds occur irregularly within the eucalypts so it would be advantageous for flies and nematodes developing within flower bud galls to have extended or variable longevities to allow fly emergences to coincide with new flower buds. Not all of the galls recorded matured to produce adult flies. Nearly half of the terminal leaf bud galls initiated were aborted, recorded as absent, parasitised or eaten (45% of initiated galls). Of the three gall forms, they were the most prone to obvious parasitism and as many as 12 hymenopteran species have been reared from terminal leaf bud galls on E. camaldulensis (Taylor et al., 1996). These galls obviously provide a resource for many species within multiple trophic levels. Fourteen percent of axial leaf bud galls were absent or eaten and birds were seen breaking off and feeding on the galls. More than half (55%) of the initiated flower bud galls disappeared during the period of observation, possibly due to the foraging of birds. Destructive sampling and rearing out of parasitoids from both axial leaf bud and flower bud gall forms is needed to establish what species exist within them. Terminal leaf bud galls ranged from 7.5 to 30.1 mm in diameter and 10.0 to 43.6 mm in length. Flower bud gall size varied, with the largest being 15.0 mm by 22.3 mm. Axial leaf bud galls, ranged from 2.6 to 13.0 mm in diameter and length ranged from 2.3 to 10.5 mm. The larger axial leaf bud galls were nodular and appeared to have multiple locules. Destructive sampling and rearing out of flies is needed to establish the relationship between size and numbers of flies emerging. Terminal leaf bud galls increased in size, including many locules and exit holes per gall. Axial leaf bud galls were much smaller than the terminal leaf bud galls and 99% had only one to three exit holes. The rounded shape and presence of few locules within the axial leaf bud galls indicate that this form is limited to a shape and size producing few flies. The observation of greater size of terminal leaf bud galls suggests that these galls may have multiple foundresses. Twelve of the 13 flower bud galls with exit holes had either one or two holes. In flower bud galls on E. camaldulensis. the operculum remains sealed and the characteristic Fergusonina “window” appears at the side of the flower bud before fly emergence through a single hole. Destructive sampling is also necessary to determine parasitism of each of the gall forms. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1331016 / Thesis (M.Sc.) -- University of Adelaide, School of Agriculture, Food and Wine, 2008

Attempts were made to grow Fergusobia nematodes in a dual aseptic culture with Eucalyptus camaldulensis. Callus tissue was grown from E. camaldulensis stem pieces in aseptic conditions. Calli were prone to deterioration after 14 days unless transferred to fresh growth medium. Lower levels of solutes (25% Murashige and Skoog salts, 25% plant vitamins and 0.5% sucrose) were more successful than published concentrations. Fergusobia J2 nematodes were surface sterilised with either Hibitane or washed with water to prepare them for inoculation of callus (Hay, 1994). Fergusobia subsequently recovered from plates of callus were all dead, which raised questions of how the nematodes are suited to Murashige and Skoog salt solutions. The survival of Fergusobia in aqueous solutions was then observed. It has been assumed that Fergusobia live about 2 days after dissection. Amphimictic nematodes from E. camaldulensis axial bud galls were used for a survival study. Nematodes lived for as long as 12 days in fresh tap water and 11 days in 1% M.S. solution. They were more active in tap water than in 1% M.S. solution. Nematodes in a dish together with dissected gall material died within 2 days. Nematodes in a separate dish with fresh tap water and clean gall fibres were observed to gather around the fibres. Observations of Fergusobia could be made within fresh solutions providing deteriorating gall tissues were removed from the dish. Gall production was attempted on E. camaldulensis grown in the glasshouse. These tree saplings were pruned to encourage new growth and periodically treated for infestations of scale insects leading to growth of sooty mould. Two forms of cage construction were used: (1) 1 m ³ screened cages and (2) acetate sleeves as used by Goolsby et al., 2000. Within the 1 m ³ cages containing flies, the growing points on saplings were blackened, possibly due to over-exploitation by ovipositing flies. One growing point caged in an acetate sleeve showed oviposition scars but did not produce a mature gall. Production of galls in the glasshouse was hindered by a lack in coincidence of flies emerging from mature galls and the flush of new growth following pruning. The production of galls within the glasshouse was not achieved. The phenology of E. camaldulensis, a host for the Fergusonina/Fergusobia mutualism, and gall ecology were observed in a two-year, non-destructive, field study in the Urrbrae Wetlands, Adelaide, South Australia. Tree growth and gall development was observed in the lower regions (0 – 2 m) of young trees. Three bud forms, terminal leaf bud, axial leaf bud and flower bud galls were monitored on the trees. The densities of galls were highly seasonal. Greatest density of growing points, axial leaf bud and flower bud galls occurred mostly during mid-winter to spring, whereas that of terminal leaf bud galls occurred during mid-spring to summer. Galling of flower buds did not appear to influence flowering and more flower buds and flowers occurred in the second year of the study as the trees matured. Trees mostly had medium (30-70%) levels of leaf damage, but there were seasonal trends in damage levels. Low scores for leaf damage were associated with increases in flower bud and flower production. Leaf damage, including sooty mould, appeared to increase during the cooler winter months. There were no significant seasonal relationships between levels of leaf damage and either growing point density or the occurrence of galls. When trees were compared with each other, those with lower leaf damage were more likely to have more growing points. The appearance of the canopy and the likelihood of a tree to have galls varied greatly between the trees. One tree was particularly susceptible to leaf attack, rarely had new leaves and produced no mature galls during the study. The colouring of leaves varied between trees, which indicates possible genetic variations causing some trees to be more likely hosts for Fergusonina/Fergusobia. Both new vegetative growth and terminal leaf bud galls were concentrated on the northern and eastern quadrants. Axial leaf bud and flower bud galls occurred more on the western or southern quadrants where they were possibly more protected from sun exposure on the northern or eastern quadrants. Axial galls on the northern side of one tree became reddened while those in the southern and western quadrants remained green. Reddening of axial galls may increase their likelihood of parasitism and predation by birds. Each of the three gall forms occurred within certain positions in the canopy. The tree host resource is partitioned effectively, with the three gall forms occurring on three different host structures. Additionally, the two vegetative forms terminal leaf bud and axial leaf bud galls occur on different shoot regions and in different seasons. The numbers of the galls is probably also affected by biotic and climatic influences. Parasitism, plant canopy shading, nutrient levels and host genetics are possible influences. Assuming an interval of 4 weeks between oviposition and first observation within the current study, terminal leaf bud galls had an average longevity of 11 weeks and axial leaf bud galls an average longevity of 14 weeks. Flower bud galls had longevities of 14 to 27 weeks from oviposition to senescence, assuming an interval of 6 weeks between oviposition and first observation within the current study. Flowers and flower buds occur irregularly within the eucalypts so it would be advantageous for flies and nematodes developing within flower bud galls to have extended or variable longevities to allow fly emergences to coincide with new flower buds. Not all of the galls recorded matured to produce adult flies. Nearly half of the terminal leaf bud galls initiated were aborted, recorded as absent, parasitised or eaten (45% of initiated galls). Of the three gall forms, they were the most prone to obvious parasitism and as many as 12 hymenopteran species have been reared from terminal leaf bud galls on E. camaldulensis (Taylor et al., 1996). These galls obviously provide a resource for many species within multiple trophic levels. Fourteen percent of axial leaf bud galls were absent or eaten and birds were seen breaking off and feeding on the galls. More than half (55%) of the initiated flower bud galls disappeared during the period of observation, possibly due to the foraging of birds. Destructive sampling and rearing out of parasitoids from both axial leaf bud and flower bud gall forms is needed to establish what species exist within them. Terminal leaf bud galls ranged from 7.5 to 30.1 mm in diameter and 10.0 to 43.6 mm in length. Flower bud gall size varied, with the largest being 15.0 mm by 22.3 mm. Axial leaf bud galls, ranged from 2.6 to 13.0 mm in diameter and length ranged from 2.3 to 10.5 mm. The larger axial leaf bud galls were nodular and appeared to have multiple locules. Destructive sampling and rearing out of flies is needed to establish the relationship between size and numbers of flies emerging. Terminal leaf bud galls increased in size, including many locules and exit holes per gall. Axial leaf bud galls were much smaller than the terminal leaf bud galls and 99% had only one to three exit holes. The rounded shape and presence of few locules within the axial leaf bud galls indicate that this form is limited to a shape and size producing few flies. The observation of greater size of terminal leaf bud galls suggests that these galls may have multiple foundresses. Twelve of the 13 flower bud galls with exit holes had either one or two holes. In flower bud galls on E. camaldulensis. the operculum remains sealed and the characteristic Fergusonina “window” appears at the side of the flower bud before fly emergence through a single hole. Destructive sampling is also necessary to determine parasitism of each of the gall forms. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1331016 / Thesis (M.Sc.) -- University of Adelaide, School of Agriculture, Food and Wine, 2008

The objective of this study was to investigate endophagous insect species richness in Fynbos. The influences of plants as determinants of insect occurrence were given special attention. The endophagous insects associated with Proteaceae in Fynbos were compared to endophage assemblages from northern, non-Capensis Proteaceae. The Cape Fynbos genus Protea is utilized by many more insect taxa than the non-Fynbos species. The high diversity of host plants in Fynbos appears to have contributed to generating high, local endophagous insect diversity. Influences of regional climate, biotope and host-plant characteristics on the frequency of occurrence of insect borers exploiting Protea species was investigated in Fynbos. Distinct differences in frequency of encounter of the various insect taxa were recorded for the various host-plants studied. This variability was primarily accounted for by physical host-plant characteristics (infructescence and seed-set variables). These findings have important implications for evolution of insects associated with these plants, as well as for the conservation of insects and in pest control programmes on indigenous cut flowers. The relative species richness of endophagous and ectophagous insects in Fynbos was compared. Gall-forming insects (Diptera: Cecidomyiidae), were found to be considerably more speciose than other feeding guilds, showing that the ratio of endophages to ectophages in sclerophyllous vegetation types is high. The intimate relationship that endophagous insects have with their host plants tends to habitat specialization. These insects are therefore likely to undergo radiation together with their host-plants. Species richness of gall-insects in Fynbos was investigated to establish whether insect richness was proportional to plant species richness. The relationship between gall-insect species richness and plant-species richness was investigated. Fynbos harboured more gall-insect species than other Cape Floristic Region vegetation types. Gall-insect species richness was positively correlated with plant-species richness. Plant species richness appears to have contributed to the evolution of a rich gall-insect fauna in the region. Fynbos gall-insect species richness is comparable to other sclerophyllous vegetation types globally, underscoring the importance of this vegetation type as a centre of galler diversification. Finally, the importance of plant species richness as a determinant of gall-insect species richness was investigated by comparing different sclerophyllous vegetation types under the same climatic conditions. Gall were sampled from Fynbos and Karoo vegetation. Fynbos had higher gall-insect species richness, correlated with plant-species richness. Plant-species richness, or the distal factors that generated it, appear to have contributed significantly to the radiation of gall-insects in this region. / Thesis (Ph.D.)-University of Natal, Pietermaritzburg, 1995.

Attempts were made to grow Fergusobia nematodes in a dual aseptic culture with Eucalyptus camaldulensis. Callus tissue was grown from E. camaldulensis stem pieces in aseptic conditions. Calli were prone to deterioration after 14 days unless transferred to fresh growth medium. Lower levels of solutes (25% Murashige and Skoog salts, 25% plant vitamins and 0.5% sucrose) were more successful than published concentrations. Fergusobia J2 nematodes were surface sterilised with either Hibitane or washed with water to prepare them for inoculation of callus (Hay, 1994). Fergusobia subsequently recovered from plates of callus were all dead, which raised questions of how the nematodes are suited to Murashige and Skoog salt solutions. The survival of Fergusobia in aqueous solutions was then observed. It has been assumed that Fergusobia live about 2 days after dissection. Amphimictic nematodes from E. camaldulensis axial bud galls were used for a survival study. Nematodes lived for as long as 12 days in fresh tap water and 11 days in 1% M.S. solution. They were more active in tap water than in 1% M.S. solution. Nematodes in a dish together with dissected gall material died within 2 days. Nematodes in a separate dish with fresh tap water and clean gall fibres were observed to gather around the fibres. Observations of Fergusobia could be made within fresh solutions providing deteriorating gall tissues were removed from the dish. Gall production was attempted on E. camaldulensis grown in the glasshouse. These tree saplings were pruned to encourage new growth and periodically treated for infestations of scale insects leading to growth of sooty mould. Two forms of cage construction were used: (1) 1 m ³ screened cages and (2) acetate sleeves as used by Goolsby et al., 2000. Within the 1 m ³ cages containing flies, the growing points on saplings were blackened, possibly due to over-exploitation by ovipositing flies. One growing point caged in an acetate sleeve showed oviposition scars but did not produce a mature gall. Production of galls in the glasshouse was hindered by a lack in coincidence of flies emerging from mature galls and the flush of new growth following pruning. The production of galls within the glasshouse was not achieved. The phenology of E. camaldulensis, a host for the Fergusonina/Fergusobia mutualism, and gall ecology were observed in a two-year, non-destructive, field study in the Urrbrae Wetlands, Adelaide, South Australia. Tree growth and gall development was observed in the lower regions (0 – 2 m) of young trees. Three bud forms, terminal leaf bud, axial leaf bud and flower bud galls were monitored on the trees. The densities of galls were highly seasonal. Greatest density of growing points, axial leaf bud and flower bud galls occurred mostly during mid-winter to spring, whereas that of terminal leaf bud galls occurred during mid-spring to summer. Galling of flower buds did not appear to influence flowering and more flower buds and flowers occurred in the second year of the study as the trees matured. Trees mostly had medium (30-70%) levels of leaf damage, but there were seasonal trends in damage levels. Low scores for leaf damage were associated with increases in flower bud and flower production. Leaf damage, including sooty mould, appeared to increase during the cooler winter months. There were no significant seasonal relationships between levels of leaf damage and either growing point density or the occurrence of galls. When trees were compared with each other, those with lower leaf damage were more likely to have more growing points. The appearance of the canopy and the likelihood of a tree to have galls varied greatly between the trees. One tree was particularly susceptible to leaf attack, rarely had new leaves and produced no mature galls during the study. The colouring of leaves varied between trees, which indicates possible genetic variations causing some trees to be more likely hosts for Fergusonina/Fergusobia. Both new vegetative growth and terminal leaf bud galls were concentrated on the northern and eastern quadrants. Axial leaf bud and flower bud galls occurred more on the western or southern quadrants where they were possibly more protected from sun exposure on the northern or eastern quadrants. Axial galls on the northern side of one tree became reddened while those in the southern and western quadrants remained green. Reddening of axial galls may increase their likelihood of parasitism and predation by birds. Each of the three gall forms occurred within certain positions in the canopy. The tree host resource is partitioned effectively, with the three gall forms occurring on three different host structures. Additionally, the two vegetative forms terminal leaf bud and axial leaf bud galls occur on different shoot regions and in different seasons. The numbers of the galls is probably also affected by biotic and climatic influences. Parasitism, plant canopy shading, nutrient levels and host genetics are possible influences. Assuming an interval of 4 weeks between oviposition and first observation within the current study, terminal leaf bud galls had an average longevity of 11 weeks and axial leaf bud galls an average longevity of 14 weeks. Flower bud galls had longevities of 14 to 27 weeks from oviposition to senescence, assuming an interval of 6 weeks between oviposition and first observation within the current study. Flowers and flower buds occur irregularly within the eucalypts so it would be advantageous for flies and nematodes developing within flower bud galls to have extended or variable longevities to allow fly emergences to coincide with new flower buds. Not all of the galls recorded matured to produce adult flies. Nearly half of the terminal leaf bud galls initiated were aborted, recorded as absent, parasitised or eaten (45% of initiated galls). Of the three gall forms, they were the most prone to obvious parasitism and as many as 12 hymenopteran species have been reared from terminal leaf bud galls on E. camaldulensis (Taylor et al., 1996). These galls obviously provide a resource for many species within multiple trophic levels. Fourteen percent of axial leaf bud galls were absent or eaten and birds were seen breaking off and feeding on the galls. More than half (55%) of the initiated flower bud galls disappeared during the period of observation, possibly due to the foraging of birds. Destructive sampling and rearing out of parasitoids from both axial leaf bud and flower bud gall forms is needed to establish what species exist within them. Terminal leaf bud galls ranged from 7.5 to 30.1 mm in diameter and 10.0 to 43.6 mm in length. Flower bud gall size varied, with the largest being 15.0 mm by 22.3 mm. Axial leaf bud galls, ranged from 2.6 to 13.0 mm in diameter and length ranged from 2.3 to 10.5 mm. The larger axial leaf bud galls were nodular and appeared to have multiple locules. Destructive sampling and rearing out of flies is needed to establish the relationship between size and numbers of flies emerging. Terminal leaf bud galls increased in size, including many locules and exit holes per gall. Axial leaf bud galls were much smaller than the terminal leaf bud galls and 99% had only one to three exit holes. The rounded shape and presence of few locules within the axial leaf bud galls indicate that this form is limited to a shape and size producing few flies. The observation of greater size of terminal leaf bud galls suggests that these galls may have multiple foundresses. Twelve of the 13 flower bud galls with exit holes had either one or two holes. In flower bud galls on E. camaldulensis. the operculum remains sealed and the characteristic Fergusonina “window” appears at the side of the flower bud before fly emergence through a single hole. Destructive sampling is also necessary to determine parasitism of each of the gall forms. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1331016 / Thesis (M.Sc.) -- University of Adelaide, School of Agriculture, Food and Wine, 2008

Inaug.-Diss.--Sofia. / Bibliography: p. [35]-38.

Este estudo investigou a ecologia de vespas parasitóides ocorrentes em galhadores Schismatodiplosis lantanae Rübsaamen, 1916 (Cecidomyiidae) em folhas de Lantana camara L. (Verbenaceae). Dessa forma, o primeiro artigo trata da ecologia comportamental da vespa parasitóide Torymus sp. (Torymidae, Hymenoptera), onde foi avaliado como as fêmeas dessa espécie defendem seu recurso de oviposição no hospedeiro. Foi analisado mudanças no comportamento devido à presença de outra fêmea coespecífica no local, ser residente do recurso, tamanho das vespas e número e tamanho das galhas através de filmagens dos experimentos realizados em laboratório. Com esse trabalho observou-se que fêmeas mudam seu comportamento quando estão na presença de um competidor em um território com hospedeiros. A estratégia de ataque foi através da ameaça, na qual suas antenas e asas são levantadas para expulsar o competidor do local. A probabilidade de haver ataques a fêmeas coespecíficas depende do tempo prévio de exploração da galha e da permanência na folha. O interesse no hospedeiro pelas invasoras foi a principal causa de conflitos com a residente. O segundo artigo trata da diversidade de vespas parasitóides e de um ciclo parasita-hospedeiro observado no período de um ano no sistema de L. camara. Foram encontradas nove espécies de vespas parasitóides, divididas em quatro famílias. Ocorreu um ciclo no parasitismo das espécies de vespas sobre seu hospedeiro no ano amostrado, podendo ser observado que são mais elevadas nos meses de Julho a Janeiro e a sobrevivência do hospedeiro foi maior nos meses de Fevereiro a Maio. As estratégias comportamentais de fêmeas de uma vespa parasitóide em relação a seus hospedeiros foram analisadas, bem como um sistema composto de diversas espécies parasitóides e sua variação no tempo. Estas observações podem contribuir para um melhor entendimento da ecologia comportamental e do padrão temporal das vespas parasitoides, e também para futuros programas de controle biológico mais eficientes. / We investigated the ecology of parasitoid wasps attacking Schismatodiplosis lantanae Rübsaamen, 1916 (Cecidomyiidae) galls on leaves of Lantana camara L. (Verbenaceae). The first article discusses the behavioral ecology of the parasitoid wasp Torymus sp. (Torymidae, Hymenoptera), reporting how their females defend oviposition resources on the hosts, changing their behavior due to the presence of a conspecific female in the patch. The identity of the wasp (resident or intruder) on the resource, female size and number and size of galls in the patch were factors studied through analysis of the behaviors revealed by video recordings of the laboratory experiments. Females change their behavior in the presence of a competitor in a territory with hosts. The strategy was to threat, raising their antennae and wings to expel the competitor of the patch. The probability of an attack on a conspecific females depended on the host exploitation time and time spent on the galled leaf. Interest in host by intruders was the main cause for conflicts. The second article reports the diversity of parasitoid wasps and a host-parasite cycle during one year period in the L. camara leaf galls system. Nine parasitoid wasp species were found, divided in four families. A cycle between parasitism and host survival was found during the sampling period. Wasp species are more abundant from July to January and host survival higher from February to May. Behavioral strategies of parasitoid wasp females toward their hosts and conspecifics have been elucidated, with the system composed of different parasitoid wasp species apparently going through an annual cycle of parasitism rate. These observations may contribute to a better understanding of parasitoid behavioral ecology and host-parasitoid dynamics, enabling more efficient future biological control programs.

Orientador: Marineide Rosa Vieira / Banca: Luiz de Souza Corrêa / Banca: Reinaldo José Fazzio Feres / Resumo: A lichia é uma fruta de grande valor econômico. A cultura da lichia pode ser muito danificada pela infestação do ácaro Aceria litchii (Keifer), sua principal praga. Pouco se conhece sobre os padrões de ocorrência e de diversidade de comunidades de ácaros associados a essa cultura no Brasil, sendo que esse conhecimento é básico e imprescindível na elaboração de propostas de manejo dessa praga. O presente trabalho teve por objetivos acompanhar a ocorrência de A. litchii em plantas de lichia no município de Casa Branca, estado de São Paulo, caracterizar os sintomas de danos decorrentes do seu desenvolvimento e identificar possíveis agentes de controle biológico dessa praga. A ocorrência de A. litchii e os danos provocados foram acompanhados em quatro árvores adultas, de 12 anos de idade, da variedade Bengal. Para isso, mensalmente, de cada planta, foram coletadas quatro extremidades de ramo com aproximadamente 0,5 m de comprimento, no período de agosto de 2008 a agosto de 2009. Os ácaros predadores foram avaliados em dois ramos de 0,30 m de comprimento. As variáveis consideradas para A. litchii foram: porcentagem de folhas atacadas, número de galhas nas folhas, número de ácaros em galhas presentes em folhas e gemas. Os predadores foram montados em lâmina de microscopia, identificados e contados. Nas galhas foram observadas formas brancas e vermelhas, ambas identificadas como A. litchii. A maior quantidade das duas formas foi registrada em outubro de 2008, com o número de formas vermelhas superando o de brancas. Ambas foram registradas em maior quantidade em folhas novas. Formas brancas em folhas novas apresentaram correlação negativa com o aumento da temperatura e da evapotranspiração. A infestação de A. litchii resultou em intensa erinose. Inicialmente surgiram eríneos claros na página inferior das folhas novas, que... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: The lychee is a fruit of great economic value. The culture of litchi can be very damaged by the infestation of the Aceria litchii (Keifer) mite, their main pest. Little is known about the patterns of occurrence and diversity of communities of mites associated with this crop in Brazil, and this knowledge is basic and essential in preparing proposals for the management of this pest. The work objectives were study the occurrence of A. litchii on litchi plants in the municipality of Casa Branca, state of Sao Paulo, to characterize the symptoms of damage resulting from its development and identify possible biological control agents of this pest. The occurrence of A. litchii and the damage caused were observed in four adult 12-year-old trees of the Bengal variety. For this four branch extremities, approximately 0.5 m long, were collected every month from each plant from August 2008 to August 2009. The predators mites were evaluate on two branches, 0.3 m long. The variables considered for A. litchii were: percentage of attacked leaves, number of galls on the leaves, number of mites present in galls on leaves and buds. Predators were mounted on microscope slide, identified and counted. In the galls were observed red and white forms, both identified as A. litchii. The greatest amount of both forms was recorded in October 2008, with the number of the red forms overcoming of the white forms. Both were recorded in larger amounts in young leaves. White forms in young leaves were negatively correlated with increasing temperature and evapotranspiration. The infestation of A. litchii resulted in intense erinose. Initially erineos were clear on the underside of young leaves, and were gradually darkening and taking the leaf surface. Galls with erineos clear were positively correlated with the number of white forms in young leaves, indicating that these... (Complete abstract click electronic access below) / Mestre

Made available in DSpace on 2014-06-11T19:29:43Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-08-04Bitstream added on 2014-06-13T18:59:25Z : No. of bitstreams: 1 picoli_prf_me_ilha.pdf: 1761844 bytes, checksum: eaddd2b5adb1968ba592dfecdc140338 (MD5) / A lichia é uma fruta de grande valor econômico. A cultura da lichia pode ser muito danificada pela infestação do ácaro Aceria litchii (Keifer), sua principal praga. Pouco se conhece sobre os padrões de ocorrência e de diversidade de comunidades de ácaros associados a essa cultura no Brasil, sendo que esse conhecimento é básico e imprescindível na elaboração de propostas de manejo dessa praga. O presente trabalho teve por objetivos acompanhar a ocorrência de A. litchii em plantas de lichia no município de Casa Branca, estado de São Paulo, caracterizar os sintomas de danos decorrentes do seu desenvolvimento e identificar possíveis agentes de controle biológico dessa praga. A ocorrência de A. litchii e os danos provocados foram acompanhados em quatro árvores adultas, de 12 anos de idade, da variedade Bengal. Para isso, mensalmente, de cada planta, foram coletadas quatro extremidades de ramo com aproximadamente 0,5 m de comprimento, no período de agosto de 2008 a agosto de 2009. Os ácaros predadores foram avaliados em dois ramos de 0,30 m de comprimento. As variáveis consideradas para A. litchii foram: porcentagem de folhas atacadas, número de galhas nas folhas, número de ácaros em galhas presentes em folhas e gemas. Os predadores foram montados em lâmina de microscopia, identificados e contados. Nas galhas foram observadas formas brancas e vermelhas, ambas identificadas como A. litchii. A maior quantidade das duas formas foi registrada em outubro de 2008, com o número de formas vermelhas superando o de brancas. Ambas foram registradas em maior quantidade em folhas novas. Formas brancas em folhas novas apresentaram correlação negativa com o aumento da temperatura e da evapotranspiração. A infestação de A. litchii resultou em intensa erinose. Inicialmente surgiram eríneos claros na página inferior das folhas novas, que... / The lychee is a fruit of great economic value. The culture of litchi can be very damaged by the infestation of the Aceria litchii (Keifer) mite, their main pest. Little is known about the patterns of occurrence and diversity of communities of mites associated with this crop in Brazil, and this knowledge is basic and essential in preparing proposals for the management of this pest. The work objectives were study the occurrence of A. litchii on litchi plants in the municipality of Casa Branca, state of Sao Paulo, to characterize the symptoms of damage resulting from its development and identify possible biological control agents of this pest. The occurrence of A. litchii and the damage caused were observed in four adult 12-year-old trees of the Bengal variety. For this four branch extremities, approximately 0.5 m long, were collected every month from each plant from August 2008 to August 2009. The predators mites were evaluate on two branches, 0.3 m long. The variables considered for A. litchii were: percentage of attacked leaves, number of galls on the leaves, number of mites present in galls on leaves and buds. Predators were mounted on microscope slide, identified and counted. In the galls were observed red and white forms, both identified as A. litchii. The greatest amount of both forms was recorded in October 2008, with the number of the red forms overcoming of the white forms. Both were recorded in larger amounts in young leaves. White forms in young leaves were negatively correlated with increasing temperature and evapotranspiration. The infestation of A. litchii resulted in intense erinose. Initially erineos were clear on the underside of young leaves, and were gradually darkening and taking the leaf surface. Galls with erineos clear were positively correlated with the number of white forms in young leaves, indicating that these... (Complete abstract click electronic access below)

Este estudo investigou a ecologia de vespas parasitóides ocorrentes em galhadores Schismatodiplosis lantanae Rübsaamen, 1916 (Cecidomyiidae) em folhas de Lantana camara L. (Verbenaceae). Dessa forma, o primeiro artigo trata da ecologia comportamental da vespa parasitóide Torymus sp. (Torymidae, Hymenoptera), onde foi avaliado como as fêmeas dessa espécie defendem seu recurso de oviposição no hospedeiro. Foi analisado mudanças no comportamento devido à presença de outra fêmea coespecífica no local, ser residente do recurso, tamanho das vespas e número e tamanho das galhas através de filmagens dos experimentos realizados em laboratório. Com esse trabalho observou-se que fêmeas mudam seu comportamento quando estão na presença de um competidor em um território com hospedeiros. A estratégia de ataque foi através da ameaça, na qual suas antenas e asas são levantadas para expulsar o competidor do local. A probabilidade de haver ataques a fêmeas coespecíficas depende do tempo prévio de exploração da galha e da permanência na folha. O interesse no hospedeiro pelas invasoras foi a principal causa de conflitos com a residente. O segundo artigo trata da diversidade de vespas parasitóides e de um ciclo parasita-hospedeiro observado no período de um ano no sistema de L. camara. Foram encontradas nove espécies de vespas parasitóides, divididas em quatro famílias. Ocorreu um ciclo no parasitismo das espécies de vespas sobre seu hospedeiro no ano amostrado, podendo ser observado que são mais elevadas nos meses de Julho a Janeiro e a sobrevivência do hospedeiro foi maior nos meses de Fevereiro a Maio. As estratégias comportamentais de fêmeas de uma vespa parasitóide em relação a seus hospedeiros foram analisadas, bem como um sistema composto de diversas espécies parasitóides e sua variação no tempo. Estas observações podem contribuir para um melhor entendimento da ecologia comportamental e do padrão temporal das vespas parasitoides, e também para futuros programas de controle biológico mais eficientes. / We investigated the ecology of parasitoid wasps attacking Schismatodiplosis lantanae Rübsaamen, 1916 (Cecidomyiidae) galls on leaves of Lantana camara L. (Verbenaceae). The first article discusses the behavioral ecology of the parasitoid wasp Torymus sp. (Torymidae, Hymenoptera), reporting how their females defend oviposition resources on the hosts, changing their behavior due to the presence of a conspecific female in the patch. The identity of the wasp (resident or intruder) on the resource, female size and number and size of galls in the patch were factors studied through analysis of the behaviors revealed by video recordings of the laboratory experiments. Females change their behavior in the presence of a competitor in a territory with hosts. The strategy was to threat, raising their antennae and wings to expel the competitor of the patch. The probability of an attack on a conspecific females depended on the host exploitation time and time spent on the galled leaf. Interest in host by intruders was the main cause for conflicts. The second article reports the diversity of parasitoid wasps and a host-parasite cycle during one year period in the L. camara leaf galls system. Nine parasitoid wasp species were found, divided in four families. A cycle between parasitism and host survival was found during the sampling period. Wasp species are more abundant from July to January and host survival higher from February to May. Behavioral strategies of parasitoid wasp females toward their hosts and conspecifics have been elucidated, with the system composed of different parasitoid wasp species apparently going through an annual cycle of parasitism rate. These observations may contribute to a better understanding of parasitoid behavioral ecology and host-parasitoid dynamics, enabling more efficient future biological control programs.