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 in | Frontiers in insect science Vol. 3; p. 1154697 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
18.04.2023
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ISSN | 2673-8600 2673-8600 |
DOI | 10.3389/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 |
Author_xml | – sequence: 1 givenname: Hannah J. surname: Broadley fullname: Broadley, Hannah J. – sequence: 2 givenname: Steven J. surname: Sipolski fullname: Sipolski, Steven J. – sequence: 3 givenname: Danielle B. surname: Pitt fullname: Pitt, Danielle B. – sequence: 4 givenname: Kim A. surname: Hoelmer fullname: Hoelmer, Kim A. – sequence: 5 givenname: Xiao-yi surname: Wang fullname: Wang, Xiao-yi – sequence: 6 givenname: Liang-ming surname: Cao fullname: Cao, Liang-ming – sequence: 7 givenname: Lisa A. surname: Tewksbury fullname: Tewksbury, Lisa A. – sequence: 8 givenname: Tyler J. surname: Hagerty fullname: Hagerty, Tyler J. – sequence: 9 givenname: Charles R. surname: Bartlett fullname: Bartlett, Charles R. – sequence: 10 givenname: Alana D. surname: Russell fullname: Russell, Alana D. – sequence: 11 givenname: Yunke surname: Wu fullname: Wu, Yunke – sequence: 12 givenname: Shannon C. surname: Davis fullname: Davis, Shannon C. – sequence: 13 givenname: Joe M. surname: Kaser fullname: Kaser, Joe M. – sequence: 14 givenname: Joseph S. surname: Elkinton fullname: Elkinton, Joseph S. – sequence: 15 givenname: Juli R. surname: Gould fullname: Gould, Juli R. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38469478$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s11829_025_10138_0 crossref_primary_10_1016_j_biocontrol_2024_105687 crossref_primary_10_3389_finsc_2023_1154651 crossref_primary_10_1016_j_biocontrol_2024_105551 crossref_primary_10_1111_brv_13130 crossref_primary_10_3389_finsc_2023_1153723 crossref_primary_10_3390_insects15110893 crossref_primary_10_1093_ee_nvae091 crossref_primary_10_1016_j_biocontrol_2025_105730 crossref_primary_10_3390_insects15110841 crossref_primary_10_1002_1438_390X_12203 |
Cites_doi | 10.5656/KSAE.2014.01.1.075 10.1007/s10340-020-01311-w 10.3157/021.125.0105 10.1093/ee/nvaa124 10.1016/j.aspen.2019.08.009 10.1093/ee/nvz110 10.1093/ee/nvab107 10.1146/annurev-ento-120220-111140 10.1016/1049-9644(92)90078-R 10.11865/zs.20150305 10.4039/Ent133429-3 10.1016/j.biocontrol.2005.06.008 10.3157/021.126.0109 10.1093/ee/nvaa137 10.1093/jisesa/iez074 10.1079/BER2001121 10.1590/S1519-566X2006000500013 10.1093/ee/16.5.1035 10.1653/024.092.0237 10.3389/finsc.2023.1134889 10.5656/KSAE.2018.08.0.035 10.1017/9781107280267 10.1007/s10340-017-0863-y 10.3390/insects10040108 10.3389/fphys.2019.00746 10.5656/KSAE.2009.48.1.053 10.1006/anbe.1998.0768 10.1093/aesa/saab030 10.1002/ps.5619 10.1073/pnas.1903579116 10.3390/f10020079 10.1007/s10526-019-09950-4 10.1007/s10340-018-0969-x 10.1038/289027a0 10.1093/aesa/88.5.666 10.3390/insects12060539 10.1111/phen.12106 10.1007/BF02374310 |
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Copyright | Copyright © 2023 Broadley, Sipolski, Pitt, Hoelmer, Wang, Cao, Tewksbury, Hagerty, Bartlett, Russell, Wu, Davis, Kaser, Elkinton and Gould. 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. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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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Title | Assessing the host range of Anastatus orientalis, an egg parasitoid of spotted lanternfly (Lycorma delicatula) using Eastern U.S. non-target species |
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