The parasitoids Pachycrepoideus vindemmiae Rondani (Hymenoptera: Pteromalidae) and Trichopria anastrephae Costa Lima (Hymenoptera: Diapriidae) have great potential in controlling Drosophila suzukii (Matsumura); however, both, compete for the same resources. In this study, we evaluated whether the different stages of development of the primary parasitoid reduce the negative effect of intrinsic competition. For this, we first defined the duration of each immature stage of both parasitoid species and then offered D. suzukii pupae containing the first parasitoid (P. vindemmiae or T. anastrephae) at different stages of development to the second parasitoid (P. vindemmiae or T. anastrephae). We also checked the second parasitoid's preference (P. vindemmiae or T. anastrephae) for the primary parasitoid at different stages of development (P. vindemmiae or T. anastrephae) or D. suzukii pupae nonparasitized. Our evaluations showed that T. anastrephae preferred to parasitize pupae that were not previously parasitized and that had not parasitized puparia of D. suzukii when P. vindemmiae was in later stage to the 1st instar. However, P. vindemmiae preferred to parasitize pupae previously parasitized by T. anastrephae. In an environment of intrinsic competition, the first parasitoid to parasitize has an advantage, except when the pupal stage of T. anastrephae is parasitized by P. vindemmiae. The variation in the parasitoids' oviposition time mitigates the competition effect; however, for use in biological control programs, the hyperparasitoids P. vindemmiae, does not prove to be advantageous, as they can affect the establishment of primary parasitoids such as T. anastrephae, and can act as competitors for resources.
{"title":"Intrinsic competition between 2 pupal parasitoids of Drosophila suzukii (Diptera: Drosophilidae)","authors":"A. Garcez, A. P. Krüger, D. E. Nava","doi":"10.1093/aesa/saad010","DOIUrl":"https://doi.org/10.1093/aesa/saad010","url":null,"abstract":"The parasitoids Pachycrepoideus vindemmiae Rondani (Hymenoptera: Pteromalidae) and Trichopria anastrephae Costa Lima (Hymenoptera: Diapriidae) have great potential in controlling Drosophila suzukii (Matsumura); however, both, compete for the same resources. In this study, we evaluated whether the different stages of development of the primary parasitoid reduce the negative effect of intrinsic competition. For this, we first defined the duration of each immature stage of both parasitoid species and then offered D. suzukii pupae containing the first parasitoid (P. vindemmiae or T. anastrephae) at different stages of development to the second parasitoid (P. vindemmiae or T. anastrephae). We also checked the second parasitoid's preference (P. vindemmiae or T. anastrephae) for the primary parasitoid at different stages of development (P. vindemmiae or T. anastrephae) or D. suzukii pupae nonparasitized. Our evaluations showed that T. anastrephae preferred to parasitize pupae that were not previously parasitized and that had not parasitized puparia of D. suzukii when P. vindemmiae was in later stage to the 1st instar. However, P. vindemmiae preferred to parasitize pupae previously parasitized by T. anastrephae. In an environment of intrinsic competition, the first parasitoid to parasitize has an advantage, except when the pupal stage of T. anastrephae is parasitized by P. vindemmiae. The variation in the parasitoids' oviposition time mitigates the competition effect; however, for use in biological control programs, the hyperparasitoids P. vindemmiae, does not prove to be advantageous, as they can affect the establishment of primary parasitoids such as T. anastrephae, and can act as competitors for resources.","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"145 - 153"},"PeriodicalIF":2.3,"publicationDate":"2023-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45730320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Dario Poier, Sharon Mitchell, Victor Tulus, Gonzalo Guillén-Gosálbez, Javier Pérez-Ramírez, Roger Marti
Scaling up syntheses from mg to kg quantities is a complex endeavor. Besides adapting laboratory protocols to industrial processes and equipment and thorough safety assessments, much attention is paid to the reduction of the process' environmental impact. For processes including transition metal catalyzed steps, e.g. cross-coupling chemistry, this impact strongly depends on the identity of the metal used. As such, a key approach is the replacement of single-use with reusable heterogeneous catalysts. Transition metal single-atom heterogeneous catalysts (SAC), a novel class of catalytic materials, might exhibit all the necessary properties to step up to this task. This article shall discuss current applications of SAC in cross-coupling chemistry from the point of a process chemist and shed light on the NCCR Catalysis contribution to the field. Investigations of the stability-activity-selectivity relationship of SACs in combination with early-stage life-cycle assessments (LCA) of potential processes lay the foundation for large-scale application tailored catalyst synthesis. Ultimately, prevailing challenges are highlighted, which need to be addressed in future research.
{"title":"Aiming for More Sustainable Cross-Coupling Chemistry by Employing Single-Atom Catalysis on Scale.","authors":"Dario Poier, Sharon Mitchell, Victor Tulus, Gonzalo Guillén-Gosálbez, Javier Pérez-Ramírez, Roger Marti","doi":"10.2533/chimia.2023.127","DOIUrl":"10.2533/chimia.2023.127","url":null,"abstract":"<p><p>Scaling up syntheses from mg to kg quantities is a complex endeavor. Besides adapting laboratory protocols to industrial processes and equipment and thorough safety assessments, much attention is paid to the reduction of the process' environmental impact. For processes including transition metal catalyzed steps, e.g. cross-coupling chemistry, this impact strongly depends on the identity of the metal used. As such, a key approach is the replacement of single-use with reusable heterogeneous catalysts. Transition metal single-atom heterogeneous catalysts (SAC), a novel class of catalytic materials, might exhibit all the necessary properties to step up to this task. This article shall discuss current applications of SAC in cross-coupling chemistry from the point of a process chemist and shed light on the NCCR Catalysis contribution to the field. Investigations of the stability-activity-selectivity relationship of SACs in combination with early-stage life-cycle assessments (LCA) of potential processes lay the foundation for large-scale application tailored catalyst synthesis. Ultimately, prevailing challenges are highlighted, which need to be addressed in future research.</p>","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"55 1","pages":"127-131"},"PeriodicalIF":1.2,"publicationDate":"2023-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82957296","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Bug zoo-keeping and scientific innovation","authors":"L. Nault","doi":"10.1093/aesa/saad008","DOIUrl":"https://doi.org/10.1093/aesa/saad008","url":null,"abstract":"","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"143 - 144"},"PeriodicalIF":2.3,"publicationDate":"2023-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41378752","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Retraction of: Symbiotic Association Between Ants and Fungus","authors":"","doi":"10.1093/aesa/saad007","DOIUrl":"https://doi.org/10.1093/aesa/saad007","url":null,"abstract":"","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"184 - 184"},"PeriodicalIF":2.3,"publicationDate":"2023-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45458255","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract The nutritional quality of herbivorous insects' food can not only directly affect the herbivorous insects themselves, but can also indirectly affect their parasitoids. To investigate these cascading, multi-trophic effects, we reared cabbage looper, Trichoplusia ni (Hübner) (Lepidoptera: Noctuidae), on artificial diets (8.1, 11.5, 16.75, 25.5, 34.25, and 43 g protein/liter diet) to assess how diet protein content affected the development of this common pest and its suitability as a host for the gregarious parasitoid, Cotesia vanessae (Reinhard) (Hymenoptera: Braconidae). Nonparasitized caterpillars experienced increased mortality when reared on 8.1 g protein/liter diet, and slower development and reduced pupal mass when reared on ≤16.75 g protein/liter diet. Host diet did not affect the percentage of hosts with parasitoid emergence nor the mass of individual parasitoids. However, parasitoid broods emerging from caterpillars reared on ≤25.5 g protein/liter diet were smaller and those reared on ≤16.75 g protein/liter diet exhibited prolonged development. The consequences of host diet on these latter F1 parasitoids did not affect their reproductive fitness. Caterpillars compensated for nutrient stress, induced by either low quality diet or parasitism, by increasing the amount of diet that they consumed. These collective results demonstrate the plasticity of host-parasitoid systems. Compensatory feeding allows the host caterpillar to moderate the consequences of low quality diets, which may subsequently affect the F1 parasitoids developing within the host, but not necessarily affect the F2 parasitoid generation. Résumé La qualité nutritionnelle de la nourriture des insectes herbivores peu non seulement affecter directement les insecte herbivores mais aussi indirectement les parasitoïdes des insectes herbivores. Pour examiner ces effets multitrophiques, nous avons élevé des larves de la fausse-arpenteuse du chou, Trichoplusia ni (Hübner) (Lepidoptera: Noctuidae), sur des milieux nutritif artificiel (8,1; 11,5; 16,75; 25,5; 34,25 et 43 g de protéine par litre) pour évaluer comment le taux de protéine du milieu nutritif affectait le développement de ce ravageur commun et sa qualité en tant qu'hôte pour le parasitoïde grégaire Cotesia vanessae (Reinhard) (Hymenoptera: Braconidae). Pour les chenilles non-parasitées, un accroissement de mortalité a été observé pour celles élevées sur le milieu nutritif contenant 8,1 g de protéines par litre, et un accroissement du temps de développement et une réduction de la masse des chrysalides ont été observé pour celles élevées sur les milieux nutritifs contenant au plus 16,75 g de protéines par litre. Le taux de protéines dans l'alimentation des chenilles n'a pas influencé le pourcentage de chenilles parasitées qui ont produits des parasitoïdes, ni la masse individuelle des parasitoïdes. Cependant, les chenilles parasitées élevées sur les milieux nutritifs contenant au plus 25,5 g de protéines par litre ont p
{"title":"Protein Deficient Diets: Cascade Effects on a Lepidopteran Pest and Its Parasitoid Wasp","authors":"V. Hervet, R. Laird, K. Floate","doi":"10.1093/aesa/saac029","DOIUrl":"https://doi.org/10.1093/aesa/saac029","url":null,"abstract":"Abstract The nutritional quality of herbivorous insects' food can not only directly affect the herbivorous insects themselves, but can also indirectly affect their parasitoids. To investigate these cascading, multi-trophic effects, we reared cabbage looper, Trichoplusia ni (Hübner) (Lepidoptera: Noctuidae), on artificial diets (8.1, 11.5, 16.75, 25.5, 34.25, and 43 g protein/liter diet) to assess how diet protein content affected the development of this common pest and its suitability as a host for the gregarious parasitoid, Cotesia vanessae (Reinhard) (Hymenoptera: Braconidae). Nonparasitized caterpillars experienced increased mortality when reared on 8.1 g protein/liter diet, and slower development and reduced pupal mass when reared on ≤16.75 g protein/liter diet. Host diet did not affect the percentage of hosts with parasitoid emergence nor the mass of individual parasitoids. However, parasitoid broods emerging from caterpillars reared on ≤25.5 g protein/liter diet were smaller and those reared on ≤16.75 g protein/liter diet exhibited prolonged development. The consequences of host diet on these latter F1 parasitoids did not affect their reproductive fitness. Caterpillars compensated for nutrient stress, induced by either low quality diet or parasitism, by increasing the amount of diet that they consumed. These collective results demonstrate the plasticity of host-parasitoid systems. Compensatory feeding allows the host caterpillar to moderate the consequences of low quality diets, which may subsequently affect the F1 parasitoids developing within the host, but not necessarily affect the F2 parasitoid generation. Résumé La qualité nutritionnelle de la nourriture des insectes herbivores peu non seulement affecter directement les insecte herbivores mais aussi indirectement les parasitoïdes des insectes herbivores. Pour examiner ces effets multitrophiques, nous avons élevé des larves de la fausse-arpenteuse du chou, Trichoplusia ni (Hübner) (Lepidoptera: Noctuidae), sur des milieux nutritif artificiel (8,1; 11,5; 16,75; 25,5; 34,25 et 43 g de protéine par litre) pour évaluer comment le taux de protéine du milieu nutritif affectait le développement de ce ravageur commun et sa qualité en tant qu'hôte pour le parasitoïde grégaire Cotesia vanessae (Reinhard) (Hymenoptera: Braconidae). Pour les chenilles non-parasitées, un accroissement de mortalité a été observé pour celles élevées sur le milieu nutritif contenant 8,1 g de protéines par litre, et un accroissement du temps de développement et une réduction de la masse des chrysalides ont été observé pour celles élevées sur les milieux nutritifs contenant au plus 16,75 g de protéines par litre. Le taux de protéines dans l'alimentation des chenilles n'a pas influencé le pourcentage de chenilles parasitées qui ont produits des parasitoïdes, ni la masse individuelle des parasitoïdes. Cependant, les chenilles parasitées élevées sur les milieux nutritifs contenant au plus 25,5 g de protéines par litre ont p","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"162 - 173"},"PeriodicalIF":2.3,"publicationDate":"2023-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49264800","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract Invertebrates that successfully colonize new habitats often share life history characteristics including high fertility, rapid development, and early maturation. Since its introduction into Florida, USA, the non-native Brown Widow, Latrodectus geometricus (Kock 1841, Araneae: Theridiidae), has rapidly expanded its range into urban areas as far north as Kansas and as far west as California. During its expansion, the Brown Widow has displaced Florida's Southern Black Widow, L. mactans (Fabricius 1775, Araneae: Tjerodoodae) and California's Western Black Widow, L. Hesperus (Chamber lin & Ivie 1935, Araneae: Theridiidae). Here, based on a field survey and controlled laboratory experiments, we report possible causes for the rapid disappearance of Florida's Southern Black Widows. Our field survey revealed that Brown Widows have twice the fertility potential as Southern Black Widows. In experiments comparing development, we show that sub-adult Brown Widows grew faster and matured earlier relative to Southern Black Widows. In our experiments on cohabitation with neighbors, bold Brown Widows were six times more likely to kill and consume shy Southern Black Widows than bold cobweb spiders and three times more likely to cohabitate with bold cobweb spiders than with shy Southern Black Widows. Our model of maternal risk-management revealed that competition for scarce prey was not a significant cause of offspring mortality for Latrodectus species. Hence, Brown Widows are not predating Black Widows or other cobweb spiders because prey is scarce. To our knowledge, this study is the first to suggest that aggressive predation by Brown Widows is a significant factor contributing to the local extinction of the shy Southern Black Widow in urban structures.
{"title":"Predation by the Introduced BrownWidow Spider (Araneae: Theridiidae) May Explain Local Extinctions of Native BlackWidows in Urban Habitats","authors":"Louis A Coticchio, R. Vetter, D. Cassill","doi":"10.1093/aesa/saad003","DOIUrl":"https://doi.org/10.1093/aesa/saad003","url":null,"abstract":"Abstract Invertebrates that successfully colonize new habitats often share life history characteristics including high fertility, rapid development, and early maturation. Since its introduction into Florida, USA, the non-native Brown Widow, Latrodectus geometricus (Kock 1841, Araneae: Theridiidae), has rapidly expanded its range into urban areas as far north as Kansas and as far west as California. During its expansion, the Brown Widow has displaced Florida's Southern Black Widow, L. mactans (Fabricius 1775, Araneae: Tjerodoodae) and California's Western Black Widow, L. Hesperus (Chamber lin & Ivie 1935, Araneae: Theridiidae). Here, based on a field survey and controlled laboratory experiments, we report possible causes for the rapid disappearance of Florida's Southern Black Widows. Our field survey revealed that Brown Widows have twice the fertility potential as Southern Black Widows. In experiments comparing development, we show that sub-adult Brown Widows grew faster and matured earlier relative to Southern Black Widows. In our experiments on cohabitation with neighbors, bold Brown Widows were six times more likely to kill and consume shy Southern Black Widows than bold cobweb spiders and three times more likely to cohabitate with bold cobweb spiders than with shy Southern Black Widows. Our model of maternal risk-management revealed that competition for scarce prey was not a significant cause of offspring mortality for Latrodectus species. Hence, Brown Widows are not predating Black Widows or other cobweb spiders because prey is scarce. To our knowledge, this study is the first to suggest that aggressive predation by Brown Widows is a significant factor contributing to the local extinction of the shy Southern Black Widow in urban structures.","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"174 - 183"},"PeriodicalIF":2.3,"publicationDate":"2023-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45294704","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Reviewers for Annals of the Entomological Society of America(November 2021–October 2022)","authors":"","doi":"10.1093/aesa/saad001","DOIUrl":"https://doi.org/10.1093/aesa/saad001","url":null,"abstract":"","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"141 - 141"},"PeriodicalIF":2.3,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41828641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"New Vision and Mission for the Annals of the ESA","authors":"D. Onstad","doi":"10.1093/aesa/saad005","DOIUrl":"https://doi.org/10.1093/aesa/saad005","url":null,"abstract":"","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"75 - 75"},"PeriodicalIF":2.3,"publicationDate":"2023-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42286020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. Honěk, I. Novák, Z. Martinková, P. Saska, J. Kulfan, M. Holecová, Terézia Jauschová, P. Zach
Abstract Using seventeen-year records of daily light trap catches of predatory Neuroptera (Chrysopidae, 13 species) and Coleoptera (Coccinellidae, 10 species), and of phytophagous Lepidoptera (Noctuidae, 79 species) we tested a hypothesis predicting that the range of annual fluctuations of catch size is greater in aphidophages, whose diet occurs irregularly and locally, than in phytophages, whose diet is available regularly and abundantly.The ranges of fluctuations of annual catches measured as the coefficient of variance (standard deviation expressed as a percentage of the average) of detrended annual catches were significantly greater in Chrysopidae (84 ± 7.1%) and Coccinellidae (121 ± 14.0%) than in Noctuidae (66 ± 2.6%). The difference between aphidophages and phytophages remained when we tested differences between the former and the samples of Noctuidae consisting only of those species whose characteristics (abundance, length and timing of flight period, number of generations per season, overwintering stage) were the same as in aphidophages. Similarly, no differences were found between sets of Noctuidae species that have characteristics (abundance, voltinism, period of flight activity) similar to aphidophages and sets of Noctuidae species that have contrary characteristics. Flight abilities of aphidophages are smaller than those of Noctuidae. As a result of this difference a light trap collects populations of aphidophages from a smaller area than populations of Noctuidae.Thus the extent of fluctuations of catch size of aphidophagous and phytophagous species is influenced both by annual differences in food availability and by differences in size of the area from which the individuals assembling to the light source are recruited.
{"title":"Trophic Ecology Drives Annual Variation in Abundance of Aphidophagous (Coccinellidae, Coleoptera and Chrysopidae, Neuroptera) and Phytophagous (Noctuidae, Lepidoptera) Insects: Evidence From Light Traps","authors":"A. Honěk, I. Novák, Z. Martinková, P. Saska, J. Kulfan, M. Holecová, Terézia Jauschová, P. Zach","doi":"10.1093/aesa/saad002","DOIUrl":"https://doi.org/10.1093/aesa/saad002","url":null,"abstract":"Abstract Using seventeen-year records of daily light trap catches of predatory Neuroptera (Chrysopidae, 13 species) and Coleoptera (Coccinellidae, 10 species), and of phytophagous Lepidoptera (Noctuidae, 79 species) we tested a hypothesis predicting that the range of annual fluctuations of catch size is greater in aphidophages, whose diet occurs irregularly and locally, than in phytophages, whose diet is available regularly and abundantly.The ranges of fluctuations of annual catches measured as the coefficient of variance (standard deviation expressed as a percentage of the average) of detrended annual catches were significantly greater in Chrysopidae (84 ± 7.1%) and Coccinellidae (121 ± 14.0%) than in Noctuidae (66 ± 2.6%). The difference between aphidophages and phytophages remained when we tested differences between the former and the samples of Noctuidae consisting only of those species whose characteristics (abundance, length and timing of flight period, number of generations per season, overwintering stage) were the same as in aphidophages. Similarly, no differences were found between sets of Noctuidae species that have characteristics (abundance, voltinism, period of flight activity) similar to aphidophages and sets of Noctuidae species that have contrary characteristics. Flight abilities of aphidophages are smaller than those of Noctuidae. As a result of this difference a light trap collects populations of aphidophages from a smaller area than populations of Noctuidae.Thus the extent of fluctuations of catch size of aphidophagous and phytophagous species is influenced both by annual differences in food availability and by differences in size of the area from which the individuals assembling to the light source are recruited.","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"125 - 140"},"PeriodicalIF":2.3,"publicationDate":"2023-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42576111","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract This review summarizes which body parts have taste function in which insect taxa. Evidence of taste by mouthparts, antennae, and tarsi is widespread. Mouthparts that commonly have taste function are the labium, including the labella and labial palps, the maxillae, including the galeae and maxillary palps, the inner surface of the labrum or clypeolabrum of chewers, and inside the precibarium/cibarium of hemipterans, which have piercing-sucking mouthparts. Tasting with mandibles has not been found, and tasting with the hypopharynx is seldom reported. Use of the antennae appears uncommon among fly species, but common among species of lepidopterans, hymenopterans, beetles, and bugs. Although tasting with legs, especially tarsi, is reported mostly for fly and lepidopteran species, there is also evidence of it for multiple species of beetles, grasshoppers, and hemipterans, and one species of a roach, an ant, and a bee. Ovipositor taste function has been supported for some species of flies, lepidopterans, hymenopterans, orthopterans, and odonates. Taste by wings has been much less studied, but has been documented in a few fly species. Taste remains unstudied for any species or any body parts of Archaeognatha, Dermaptera, Mantodea, Mecoptera, Phasmatodea, Megaloptera, Neuroptera, Phthiraptera, Psocoptera, Siphonaptera, as well as Raphidioptera, Strepsiptera, Embioptera, Notoptera, and Zoraptera. Across holometabolous insects, larvae have not often been examined, the exception being some species of lepidopterans, flies, and beetles. Taste studies of antenna and legs are uncommon for even lepidopteran and beetle larvae.
{"title":"Gustation Across the Class Insecta: Body Locations","authors":"B. King, P. Gunathunga","doi":"10.1093/aesa/saac027","DOIUrl":"https://doi.org/10.1093/aesa/saac027","url":null,"abstract":"Abstract This review summarizes which body parts have taste function in which insect taxa. Evidence of taste by mouthparts, antennae, and tarsi is widespread. Mouthparts that commonly have taste function are the labium, including the labella and labial palps, the maxillae, including the galeae and maxillary palps, the inner surface of the labrum or clypeolabrum of chewers, and inside the precibarium/cibarium of hemipterans, which have piercing-sucking mouthparts. Tasting with mandibles has not been found, and tasting with the hypopharynx is seldom reported. Use of the antennae appears uncommon among fly species, but common among species of lepidopterans, hymenopterans, beetles, and bugs. Although tasting with legs, especially tarsi, is reported mostly for fly and lepidopteran species, there is also evidence of it for multiple species of beetles, grasshoppers, and hemipterans, and one species of a roach, an ant, and a bee. Ovipositor taste function has been supported for some species of flies, lepidopterans, hymenopterans, orthopterans, and odonates. Taste by wings has been much less studied, but has been documented in a few fly species. Taste remains unstudied for any species or any body parts of Archaeognatha, Dermaptera, Mantodea, Mecoptera, Phasmatodea, Megaloptera, Neuroptera, Phthiraptera, Psocoptera, Siphonaptera, as well as Raphidioptera, Strepsiptera, Embioptera, Notoptera, and Zoraptera. Across holometabolous insects, larvae have not often been examined, the exception being some species of lepidopterans, flies, and beetles. Taste studies of antenna and legs are uncommon for even lepidopteran and beetle larvae.","PeriodicalId":8076,"journal":{"name":"Annals of The Entomological Society of America","volume":"116 1","pages":"76 - 82"},"PeriodicalIF":2.3,"publicationDate":"2023-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47064968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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