Assessing the host range of Anastatus orientalis, an egg parasitoid of spotted lanternfly (Lycorma delicatula) using Eastern U.S. non-target species

The spotted lanternfly, Lycorma delicatula (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many surrounding states despite quarantines and control efforts, and further spread is anticipated. A classical (importation) biological control program...

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Published inFrontiers in insect science Vol. 3; p. 1154697
Main Authors Broadley, Hannah J., Sipolski, Steven J., Pitt, Danielle B., Hoelmer, Kim A., Wang, Xiao-yi, Cao, Liang-ming, Tewksbury, Lisa A., Hagerty, Tyler J., Bartlett, Charles R., Russell, Alana D., Wu, Yunke, Davis, Shannon C., Kaser, Joe M., Elkinton, Joseph S., Gould, Juli R.
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 18.04.2023
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Online AccessGet full text
ISSN2673-8600
2673-8600
DOI10.3389/finsc.2023.1154697

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Abstract The spotted lanternfly, Lycorma delicatula (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many surrounding states despite quarantines and control efforts, and further spread is anticipated. A classical (importation) biological control program would contribute to the long-term management of L. delicatula in the eastern U.S. In its native range of China, Anastatus orientalis (Hymenoptera: Eupelmidae), an egg parasitoid, causes significant mortality. Anastatus orientalis consists of multiple haplotypes that differ in important biological parameters. To delineate the physiological host range of A. orientalis Haplotype C, we completed no-choice and choice testing. No-choice testing of non-target eggs from 36 insect species spanning six orders and 18 families showed that physiologically this haplotype of A. orientalis can develop in a variety of host species eggs from the families Coreidae, Fulgoridae, Pentatomidae, and Saturniidae. Ten of the 16 species that were attacked in the no-choice tests were also attacked in the choice tests. The production of progeny on non-target egg masses was significantly lower than on the controls ( L. delicatula egg masses run simultaneously) in the no-choice and choice tests. For the non-target species that were attacked and resulted in female wasp progeny, these females were able to produce their own progeny at the same rate as control females that were reared from the L. delicatula eggs. Larger host eggs corresponded to an increased female-biased sex ratio of the progeny, suggesting that gravid females select them for fertilized eggs. Results from these studies suggest that A. orientalis Haplotype C prefers to parasitize L. delicatula egg masses but is capable of developing in some non-target species.
AbstractList The spotted lanternfly, Lycorma delicatula (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many surrounding states despite quarantines and control efforts, and further spread is anticipated. A classical (importation) biological control program would contribute to the long-term management of L. delicatula in the eastern U.S. In its native range of China, Anastatus orientalis (Hymenoptera: Eupelmidae), an egg parasitoid, causes significant mortality. Anastatus orientalis consists of multiple haplotypes that differ in important biological parameters. To delineate the physiological host range of A. orientalis Haplotype C, we completed no-choice and choice testing. No-choice testing of non-target eggs from 36 insect species spanning six orders and 18 families showed that physiologically this haplotype of A. orientalis can develop in a variety of host species eggs from the families Coreidae, Fulgoridae, Pentatomidae, and Saturniidae. Ten of the 16 species that were attacked in the no-choice tests were also attacked in the choice tests. The production of progeny on non-target egg masses was significantly lower than on the controls ( L. delicatula egg masses run simultaneously) in the no-choice and choice tests. For the non-target species that were attacked and resulted in female wasp progeny, these females were able to produce their own progeny at the same rate as control females that were reared from the L. delicatula eggs. Larger host eggs corresponded to an increased female-biased sex ratio of the progeny, suggesting that gravid females select them for fertilized eggs. Results from these studies suggest that A. orientalis Haplotype C prefers to parasitize L. delicatula egg masses but is capable of developing in some non-target species.
The spotted lanternfly, (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many surrounding states despite quarantines and control efforts, and further spread is anticipated. A classical (importation) biological control program would contribute to the long-term management of in the eastern U.S. In its native range of China, (Hymenoptera: Eupelmidae), an egg parasitoid, causes significant mortality. consists of multiple haplotypes that differ in important biological parameters. To delineate the physiological host range of Haplotype C, we completed no-choice and choice testing. No-choice testing of non-target eggs from 36 insect species spanning six orders and 18 families showed that physiologically this haplotype of can develop in a variety of host species eggs from the families Coreidae, Fulgoridae, Pentatomidae, and Saturniidae. Ten of the 16 species that were attacked in the no-choice tests were also attacked in the choice tests. The production of progeny on non-target egg masses was significantly lower than on the controls ( egg masses run simultaneously) in the no-choice and choice tests. For the non-target species that were attacked and resulted in female wasp progeny, these females were able to produce their own progeny at the same rate as control females that were reared from the eggs. Larger host eggs corresponded to an increased female-biased sex ratio of the progeny, suggesting that gravid females select them for fertilized eggs. Results from these studies suggest that Haplotype C prefers to parasitize egg masses but is capable of developing in some non-target species.
The spotted lanternfly, Lycorma delicatula (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many surrounding states despite quarantines and control efforts, and further spread is anticipated. A classical (importation) biological control program would contribute to the long-term management of L. delicatula in the eastern U.S. In its native range of China, Anastatus orientalis (Hymenoptera: Eupelmidae), an egg parasitoid, causes significant mortality. Anastatus orientalis consists of multiple haplotypes that differ in important biological parameters. To delineate the physiological host range of A. orientalis Haplotype C, we completed no-choice and choice testing. No-choice testing of non-target eggs from 36 insect species spanning six orders and 18 families showed that physiologically this haplotype of A. orientalis can develop in a variety of host species eggs from the families Coreidae, Fulgoridae, Pentatomidae, and Saturniidae. Ten of the 16 species that were attacked in the no-choice tests were also attacked in the choice tests. The production of progeny on non-target egg masses was significantly lower than on the controls (L. delicatula egg masses run simultaneously) in the no-choice and choice tests. For the non-target species that were attacked and resulted in female wasp progeny, these females were able to produce their own progeny at the same rate as control females that were reared from the L. delicatula eggs. Larger host eggs corresponded to an increased female-biased sex ratio of the progeny, suggesting that gravid females select them for fertilized eggs. Results from these studies suggest that A. orientalis Haplotype C prefers to parasitize L. delicatula egg masses but is capable of developing in some non-target species.The spotted lanternfly, Lycorma delicatula (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many surrounding states despite quarantines and control efforts, and further spread is anticipated. A classical (importation) biological control program would contribute to the long-term management of L. delicatula in the eastern U.S. In its native range of China, Anastatus orientalis (Hymenoptera: Eupelmidae), an egg parasitoid, causes significant mortality. Anastatus orientalis consists of multiple haplotypes that differ in important biological parameters. To delineate the physiological host range of A. orientalis Haplotype C, we completed no-choice and choice testing. No-choice testing of non-target eggs from 36 insect species spanning six orders and 18 families showed that physiologically this haplotype of A. orientalis can develop in a variety of host species eggs from the families Coreidae, Fulgoridae, Pentatomidae, and Saturniidae. Ten of the 16 species that were attacked in the no-choice tests were also attacked in the choice tests. The production of progeny on non-target egg masses was significantly lower than on the controls (L. delicatula egg masses run simultaneously) in the no-choice and choice tests. For the non-target species that were attacked and resulted in female wasp progeny, these females were able to produce their own progeny at the same rate as control females that were reared from the L. delicatula eggs. Larger host eggs corresponded to an increased female-biased sex ratio of the progeny, suggesting that gravid females select them for fertilized eggs. Results from these studies suggest that A. orientalis Haplotype C prefers to parasitize L. delicatula egg masses but is capable of developing in some non-target species.
Author Pitt, Danielle B.
Broadley, Hannah J.
Sipolski, Steven J.
Wang, Xiao-yi
Davis, Shannon C.
Wu, Yunke
Elkinton, Joseph S.
Hagerty, Tyler J.
Kaser, Joe M.
Gould, Juli R.
Russell, Alana D.
Hoelmer, Kim A.
Cao, Liang-ming
Tewksbury, Lisa A.
Bartlett, Charles R.
AuthorAffiliation 7 Department of Ecology and Evolutionary Biology, Cornell University , Ithaca, NY , United States
3 Beneficial Insects Introduction Research Unit, United States Department of Agriculture, Agricultural Research Service , Newark, DE , United States
6 Department of Entomology and Wildlife Ecology, University of Delaware , Newark, DE , United States
1 Forest Pest Methods Laboratory, United States Department of Agriculture, Animal and Plant Health Inspection Service, Plant Protection and Quarantine, Science and Technology , Buzzards Bay, MA , United States
2 Department of Environmental Conservation, University of Massachusetts , Amherst, MA , United States
4 Key Laboratory of Forest Protection of National Forestry and Grassland Administration, Ecology and Nature Conservation Institute, Chinese Academy of Forestry , Beijing , China
5 Department of Plant Sciences and Entomology, University of Rhode Island , Kingston, RI , United States
AuthorAffiliation_xml – name: 4 Key Laboratory of Forest Protection of National Forestry and Grassland Administration, Ecology and Nature Conservation Institute, Chinese Academy of Forestry , Beijing , China
– name: 5 Department of Plant Sciences and Entomology, University of Rhode Island , Kingston, RI , United States
– name: 7 Department of Ecology and Evolutionary Biology, Cornell University , Ithaca, NY , United States
– name: 1 Forest Pest Methods Laboratory, United States Department of Agriculture, Animal and Plant Health Inspection Service, Plant Protection and Quarantine, Science and Technology , Buzzards Bay, MA , United States
– name: 2 Department of Environmental Conservation, University of Massachusetts , Amherst, MA , United States
– name: 6 Department of Entomology and Wildlife Ecology, University of Delaware , Newark, DE , United States
– name: 3 Beneficial Insects Introduction Research Unit, United States Department of Agriculture, Agricultural Research Service , Newark, DE , United States
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Copyright © 2023 Broadley, Sipolski, Pitt, Hoelmer, Wang, Cao, Tewksbury, Hagerty, Bartlett, Russell, Wu, Davis, Kaser, Elkinton and Gould 2023 Broadley, Sipolski, Pitt, Hoelmer, Wang, Cao, Tewksbury, Hagerty, Bartlett, Russell, Wu, Davis, Kaser, Elkinton and Gould
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Keywords natural enemy
Eupelmidae
Fulgoridae
biological control
invasive species
Language English
License Copyright © 2023 Broadley, Sipolski, Pitt, Hoelmer, Wang, Cao, Tewksbury, Hagerty, Bartlett, Russell, Wu, Davis, Kaser, Elkinton and Gould.
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Reviewed by: Osariyekemwen Uyi, University of Benin, Nigeria; Kier Klepzig, University of Georgia, United States
Edited by: Frank H. Koch, Forest Service (USDA), United States
This article was submitted to Invasive Insect Species, a section of the journal Frontiers in Insect Science
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Snippet The spotted lanternfly, Lycorma delicatula (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many...
The spotted lanternfly, (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many surrounding states...
The spotted lanternfly, Lycorma delicatula (Hemiptera: Fulgoridae), an invasive planthopper discovered in Pennsylvania, U.S. in 2014, has spread to many...
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SubjectTerms Insect Science
Title Assessing the host range of Anastatus orientalis, an egg parasitoid of spotted lanternfly (Lycorma delicatula) using Eastern U.S. non-target species
URI https://www.ncbi.nlm.nih.gov/pubmed/38469478
https://www.proquest.com/docview/2956158247
https://pubmed.ncbi.nlm.nih.gov/PMC10926408
Volume 3
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