Biological Control of Invasive Aquatic and Wetland Plants by Arthropods: a Meta-Analysis of Data from the Last Three Decades

Total Page:16

File Type:pdf, Size:1020Kb

Biological Control of Invasive Aquatic and Wetland Plants by Arthropods: a Meta-Analysis of Data from the Last Three Decades BioControl DOI 10.1007/s10526-011-9393-3 Biological control of invasive aquatic and wetland plants by arthropods: a meta-analysis of data from the last three decades Justin L. Reeves • Patrick D. Lorch Received: 2 February 2011 / Accepted: 4 July 2011 Ó International Organization for Biological Control (IOBC) 2011 Abstract Results from the last three decades of more years) and non-target effect studies could also aquatic and wetland plant biological control by be performed in the future. arthropods were combined using meta-analytical techniques to provide an objective, quantitative Keywords Meta-analysis Á Biological control Á understanding of control efficacy that cannot be Aquatic Á Wetland Á Plant Á Insect provided by available narrative reviews. Analyses were performed to determine if differences exist in how well diverse biocontrol agents perform, and if Introduction experimental design can impact study results. Across all analyses, biocontrol of the included plants was Classical biological control can provide the most generally successful. Though little heterogeneity in ecologically and economically sound methodology efficacy was seen between the individual biocontrol for controlling invasive plants and their negative agents used, all experimental design analyses showed impacts (McFadyen 1998). Recent evaluations of significant differences between respective study biological control of plants (both terrestrial and types. Thus, study design can significantly impact aquatic) have identified a range of factors correlated the results of biocontrol studies. From these results, with effectiveness, but these studies have either been we suggest that field studies with controls be qualitative (e.g., Andres and Bennett 1975; McFa- performed using subsamples of an area (quadrats, dyen 1998; others listed in Cuda et al. 2008)or transects, etc.), with biomass or density being the quantitative but did not compare data within or plant variable measured. More long-term (two or between individual invasive plant and control agent species (Stiling and Cornelissen 2005). Particularly for biological control of invasive aquatic plants, Handling Editor: John Scott many general factors have been shown to influence biological control of a wide range of plant species. J. L. Reeves Á P. D. Lorch Abiotic factors such as climate, habitat conditions, Department of Biological Sciences, Kent State University, Kent, OH 44242, USA and concurrent management tactics such as mechan- ical harvesting or pesticide application have been Present Address: shown to influence biological control efficacy in & J. L. Reeves ( ) multiple systems. Similarly, biotic factors such as Department of Biology, Colorado State University, Fort Collins, CO 80523, USA host-plant quality or genotype, biological control e-mail: [email protected] agent density, and agent mortality factors such as 123 J. L. Reeves, P. D. Lorch predation, parasitism, or disease can also influence reviews of aquatic plant biological control (e.g., control efficacy. More specifically, successful bio- Andres and Bennett 1975; Cuda et al. 2008). Both logical control of water hyacinth (Eichhornia crass- aquatic and wetland plants were included here pies), may be dependent on control agent (larval) because it can be difficult to differentiate between density as well, while larval density is in turn the two plant types (Cuda et al. 2008). Heterogeneity impacted by plant status (Wilson et al. 2006). A between arthropod agents was tested to determine if qualitative review of all of these factors, along with there are any differences in how well the various an overview of the field of biological control of biological control agents have performed when submersed aquatic plants, is provided by Cuda et al. compared to one another (which may help decide (2008). which agents to use for which plants), or at least Though the many factors above have been found which agents have had a significant effect on their to potentially impact biological control efficacy of target plant. Further, because of the wide variety of plants in general, much work still needs to be done, methods that have been used to quantify effects of particularly for aquatic plants (Cuda et al. 2008). biological control agents on their target plants, it was Quantitative reviews of the literature may help to hypothesized that experimental design may influence more fully understand control efficacy and go beyond biological control efficacy. To test this, we quantified the general claims of successful biological control of differences in effect across agents based on experi- aquatic plants that have come from narrative reviews mental design factors such as use of one versus two such as McFadyen (1998). This may be especially biological control agents, experimental (with con- true for understanding how differences in control trols) versus observational (without controls) studies, efficacy depend on which agent is used, or on lab versus field studies, the response variable mea- experimental design, both of which are factors on sured (e.g., plant density, biomass, percent cover, which little or no work (especially quantitative work) weight change, leaf area grazed), the type of replicate has been done on aquatic plants. used (whole lake, subsample of an area, aquaria, or Meta-analysis provides a method for quantitatively individual plants), and finally the study duration. Data synthesizing the results of independent experiments to from the last three decades of biological control work draw general conclusions (see Cooper and Hedges published in a wide variety of journals were used to 1994; Gurevitch and Hedges 2001). Because meta- empirically test these hypotheses and provide a more analysis can be a useful tool for understanding patterns objective exploration of aquatic plant biological across multiple studies, it has been used in many control efficacy than can be provided by narrative ecological fields, including biological control (Stiling reviews. and Cornelissen 2005). Though the meta-analysis performed by Stiling and Cornelissen (2005) included a categorical analysis of weed biological control that Materials and methods showed general control success, it was not specific to aquatic or wetland invasive plants (the plant species Standard meta-analysis techniques were used for this included were not listed), nor were invasive plants the study following Gurevitch and Hedges (2001). Liter- main focus of the study (the study covered the entire ature search methods, data inclusion methods, and field of biological control of all types of organisms). measures to avoid non-independence of data are often There were also no analyses performed to specifically underreported in meta-analysis papers, so included compare individual biological control agent species, below are specific sections to detail these aspects of which can be important in deciding which agents to this study. use for which plants, or at least in examining which agents have worked and which have not. Literature search The purpose of the work presented here was to broadly quantify the efficacy of biological control An extensive list of specialist arthropod biological agents specifically of invasive aquatic and wetland control agents (both candidate agents and currently plants using meta-analytical techniques. This effort employed agents) and their corresponding target was designed to improve on previous narrative invasive aquatic and wetland plants was built through 123 Biological control of invasive aquatic and wetland plants 0.4 history even if no plant data were reported), 126 181 articles reported some sort of agent effects on plants 0.3 (any plant effect measured was included at this stage; some papers in Fig. 1 were included in both lab and field categories when necessary). Of these 126 111 0.2 103 91 articles, 53 articles provided 62 data points appro- 76 priate for meta-analysis (Appendix Table 3) using the 53 data inclusion and analysis methods described below. 0.1 44 38 Proportion of Studies The large discrepancy between the total number of 20 papers and papers with appropriate data for analysis 0.0 ) t t s was a result of searching by agent names rather than n lab rs) ition men nces s p e me ts: +y lo u vipo e fl fec (2 t effect o blish ts e control-type terms like ‘‘biological control’’. This host range) ev c in a ffects: field c . d ti st e fe arg d e f -t (incl. bio n e r an a o term ef on o y / ti rm n was done to make sure papers were not excluded due i it ic la te av nd iot u short g h b op short-term be p lon fecu to the choice of search terms (Cooper and Hedges life history (incl d Study Category 1994), giving as broad an overview of the literature as dist. an possible (as in Stiling and Cornelissen 2005). For the Fig. 1 Categories used to organize papers from literature articles with appropriate data, the models used here search and their overall proportion of the entire set of papers tested for differences in control efficacy based on the (n = 541). Categories were not mutually exclusive, and studies were placed in all appropriate categories. The numbers above biological control agent used (Appendix Table 2). each bar represent the number of studies associated with that Similarly, to examine the impact of experimental respective category design on biological control efficacy across agents, the models used here quantified and compared the intensive internet and literature searches and cross effects of whether one or two biological control referenced with Julien and Griffiths (1998) to make agents were used concurrently in the study, the type sure no agents (or at least agents with published of control used [initial value (observational studies) articles containing biological control data) were or ‘‘real’’ control (experimental studies)], whether the missed. Once the list of agents and plants was study was performed in the lab or field, the response compiled (Appendix Table 2), the literature search variable measured (biomass, density, percent cover, for studies to be used for the meta-analyses was or other related measures), the replicate type used performed in two well-known, comprehensive dat- (individual plant, aquarium, sub-samples of an area, abases: ISI Web of Science and Biological Abstracts.
Recommended publications
  • Assessing the Risk to Neptunia Oleracea Lour. by the Moth, Neurostrota Gunniella (Busck), a Biological Control Agent for Mimosa Pigra L
    Proceedings of the X International Symposium on Biological Control of Weeds 449 4-14 July 1999, Montana State University, Bozeman, Montana, USA Neal R. Spencer [ed.]. pp. 449-457 (2000) Assessing the Risk to Neptunia oleracea Lour. by the Moth, Neurostrota gunniella (Busck), a Biological Control Agent for Mimosa pigra L. I. W. FORNO1, J. FICHERA1, and S. PRIOR2 1CSIRO Entomology, PMB 3, Indooroopilly Q4069, Australia 2Present Address: Department of Natural Resources, Magazine Street, Sherwood Q4075, Australia Abstract Mimosa pigra L. is native to tropical America and is an aggressive, invasive weed on the flood plains of the Northern Territory of Australia and in several countries in Southeast Asia. Neurostrota gunniella (Busck) (Gracillariidae) was introduced into Australia from Mexico in 1986 for biological control of mimosa. It was released in 1989 following com- pletion of extensive host range studies which determined that the moth bred readily on M. pigra and to a much lesser extent on Neptunia dimorphantha Domin, N. gracilis Benth., N. major (Benth.) Windler, N. monosperma F. Muell. and M. pudica L. Damage to these non-target species was assessed as insignificant. Subsequently, this moth was introduced to Thailand where quarantine studies showed substantial attack on an important vegetable, N. oleracea Lour., which is a perennial, aquatic herb which either grows prostrate near the water’s edge or floats by forming spongy aerenchyma around the stems. N. gunniella was not released in Southeast Asia. Further studies showed that N. gunniella oviposits and breeds similarly on potted M. pigra and the terrestrial form of N. oleracea but fewer eggs are laid and larval mortality is much greater on N.
    [Show full text]
  • Biological Control of Water Hyacinth with Arthropods: a Review to 2000
    Biological Control of Water Hyacinth with Arthropods: a Review to 2000 M.H. Julien* Abstract Water hyacinth, native to the Amazon River, invaded the tropical world over the last century and has become an extremely serious weed. The search for biological control agents began in the early 1960s and continues today. Six arthropod species have been released around the world. They are: two weevils, Neochetina bruchi and N. eichhorniae; two moths, Niphograpta albiguttalis and Xubida infusellus; a mite Orthogalumna terebrantis; and a bug Eccritotarsus catarinensis. The mite and X. infusellus have not contributed to control and the bug is under evaluation following recent releases in Africa. The two weevils and the moth N. albiguttalis have been released in numerous infestations since the 1970s and have contributed to successful control of the weed in many locations. It is timely to assess their impact on water hyacinth and, to help in planning future strategies, to identify the factors that contribute to or mitigate against successful biological control. Although the search for new agents continues, and as a result biological control will likely be improved, this technique alone is unlikely to be successful in all of the weed’s habitats. It is important that whole-of-catchment management strategies be developed that integrate biological control with other control techniques. The aims of such strategies should be to achieve the best possible control using methods that are affordable and sustainable; hence the need to develop strategies using biological control as the base component. WATER hyacinth apparently became a problem in the sation of the weed for commercial and subsistence USA following its distribution to participants in the purposes has also been widely considered.
    [Show full text]
  • Forest Health Technology Enterprise Team Biological Control of Invasive
    Forest Health Technology Enterprise Team TECHNOLOGY TRANSFER Biological Control Biological Control of Invasive Plants in the Eastern United States Roy Van Driesche Bernd Blossey Mark Hoddle Suzanne Lyon Richard Reardon Forest Health Technology Enterprise Team—Morgantown, West Virginia United States Forest FHTET-2002-04 Department of Service August 2002 Agriculture BIOLOGICAL CONTROL OF INVASIVE PLANTS IN THE EASTERN UNITED STATES BIOLOGICAL CONTROL OF INVASIVE PLANTS IN THE EASTERN UNITED STATES Technical Coordinators Roy Van Driesche and Suzanne Lyon Department of Entomology, University of Massachusets, Amherst, MA Bernd Blossey Department of Natural Resources, Cornell University, Ithaca, NY Mark Hoddle Department of Entomology, University of California, Riverside, CA Richard Reardon Forest Health Technology Enterprise Team, USDA, Forest Service, Morgantown, WV USDA Forest Service Publication FHTET-2002-04 ACKNOWLEDGMENTS We thank the authors of the individual chap- We would also like to thank the U.S. Depart- ters for their expertise in reviewing and summariz- ment of Agriculture–Forest Service, Forest Health ing the literature and providing current information Technology Enterprise Team, Morgantown, West on biological control of the major invasive plants in Virginia, for providing funding for the preparation the Eastern United States. and printing of this publication. G. Keith Douce, David Moorhead, and Charles Additional copies of this publication can be or- Bargeron of the Bugwood Network, University of dered from the Bulletin Distribution Center, Uni- Georgia (Tifton, Ga.), managed and digitized the pho- versity of Massachusetts, Amherst, MA 01003, (413) tographs and illustrations used in this publication and 545-2717; or Mark Hoddle, Department of Entomol- produced the CD-ROM accompanying this book.
    [Show full text]
  • Crambidae: Lepidoptera) of Ohio: Characterization, Host Associations and Revised Species Accounts
    Crambinae (Crambidae: Lepidoptera) of Ohio: Characterization, Host Associations and Revised Species Accounts THESIS Presented in Partial Fulfillment of the Requirements for the Degree Master of Science in the Graduate School of The Ohio State University By Devon A Rogers Graduate Program in Entomology The Ohio State University 2014 Master's Examination Committee: Dr. David J. Shetlar - Advisor Dr. Steve Passoa Dr. Andy Michel Dr. Dave Gardiner Copyright by Devon Ashley Rogers 2014 Abstract A review of the North American Crambinae sod webworm taxonomy, phylogenetic history, and biology is presented. Traditional analysis, combined with modern genetic analysis has changed and solidified the placement of these species. Previously cryptic and unidentifiable larvae were identified using genetic analysis of the mitochondrial CO1 gene and an evaluation of potential host plant associations is given. DNA sequencing is a useful tool that can be used to identify unknown sod webworm larvae, including the especially difficult to identify first and second instar larvae. Only Parapediasia teterrella larvae were recovered from the short-cut, golf course-type, creeping bentgrass (Agrostis stolonifera), as was a single Agriphila ruricolella. Fissicrambus mutabilis was obtained from lawn-height Kentucky bluegrass (Poa pratensis) and turf type tall fescue (Festuca arundinacea). Sod webworm adults were monitored with a standard blacklight trap between 2009 and 2013. Each year 14 species were recovered from the light trap. Species obtained from the managed turfgrass yielded only a fraction of the number of species attracted to the light trap. The sod webworm species Euchromius ocellus first appeared in late 2012. This is a first report for this species in Ohio.
    [Show full text]
  • Varneria Dyar 1904 Platytes Acerata Dyar 1917 Syn
    840 NOMINA INSECTA NEARCTICA Varneria Dyar 1904 Platytes acerata Dyar 1917 Syn. Xubida punctilineella Barnes and McDunnough 1913 (Platytes) Varneria atrifasciella Barnes and McDunnough 1913 (Varneria) Xubida puritella Kearfott 1908 (Chilo) Varneria postremella Dyar 1904 (Varneria) Platytes dinephelalis Dyar 1917 Syn. Xubida relovae Klots 1970 (Xubida) Vaxi Bleszynski 1962 Yosemitia Ragonot 1901 Vaxi auratellus Clemens 1860 (Crambus) Yosemetia Hulst 1903 Missp. Urola pulchella Walker 1863 Syn. Vaxi critica Forbes 1820 (Argyria) Yosemitia fieldiella Dyar 1913 (Zophodia) Yosemitia graciella Hulst 1887 (Spermatophora) Vitula Ragonot 1887 Yosemitia longipennella Hulst 1888 (Zophodia) Hornigia Ragonot 1887 Homo. Manhatta Hulst 1890 Syn. Zaboba Dyar 1914 Eccopsia Hulst 1903 Syn. Zaboba mitchelli Dyar 1914 (Zaboba) Vitula aegerella Neunzig 1990 (Vitula) Zaboba unicoloralis Munroe 1970 (Zaboba) Vitula broweri Heinrich 1956 (Manhatta) Vitula coconinoana Neunzig 1990 (Vitula) Zamagiria Dyar 1914 Vitula edmandsii Packard 1864 (Nephopteryx) Vitula dentosella Ragonot 1887 Syn. Zamagiria australella Hulst 1900 (Selagia) Vitula serratilineella Ragonot 1887 Syn. Immyria bumeliella Barnes and McDunnough 1913 Syn. Vitula bombylicolella Amsel 1955 Syn. Zamagiria kendalli Blanchard 1970 (Zamagiria) Vitula edmandsae Heinrich 1956 Emend. Zamagiria laidion Zeller 1881 (Myelois) Vitula insula Neunzig 1990 (Vitula) Zamagiria deia Dyar 1919 Syn. Vitula lugubrella Ragonot 1887 (Hornigia) Zamagiria striella Dyar 1919 Syn. Vitula pinei Heinrich 1956 (Vitula) Vitula setonella McDunnough 1927 (Moodna) Zophodia Hübner 1825 Dakruma Grote 1878 Syn. Volatica Heinrich 1956 Zophodia convulutella Hübner 1796 (Tinea) Volatica gallivorella Neunzig 1990 (Volatica) Tinea grossulariella Hübner 1809 Syn. Zophodia grossularialis Hübner 1825 Emend. Wakulla Shaffer 1968 Pempelia grossulariae Riley 1829 Syn. Dakruma turbatella Grote 1878 Syn. Wakulla carneella Barnes and McDunnough 1913 (Bandera) Euzophera franconiella Hulst 1890 Syn.
    [Show full text]
  • Plant Finding Behavior by Insects and Biological
    PLANT FINDING BEHAVIOR OF PHYTOPHAGOUS INSECTS AND BIOLOGICAL CONTROL OF AQUATIC PLANTS A dissertation submitted to Kent State University in partial fulfillment of the requirements for the degree of Doctor of Philosophy by Justin L. Reeves December 2010 Dissertation written by Justin L. Reeves B.A., Western State College of Colorado, 2006 Ph.D., Kent State University, 2010 Approved by Patrick D. Lorch , Chair, Doctoral Dissertation Committee Mark W. Kershner , Members, Doctoral Dissertation Committee Ferenc A. de Szalay _ Marilyn A. Norconk _ Accepted by James L. Blank , Chair, Department of Biological Sciences John R. D. Stalvey , Dean, College of Arts and Sciences ii TABLE OF CONTENTS LIST OF FIGURES………………………………………………….…………………...vi LIST OF TABLES……………………………………………………………………...viii ACKNOWLEDGMENTS………………………………………………………….……..x CHAPTER I. Introduction………………………………………………………….….…1 II. Biological control of invasive aquatic and wetland plants by arthropods: a meta-analysis of data from the last three decades…………...………..…9 Abstract…………………………………………………………....9 Introduction .………………………………………………….….10 Methods…………………………………………………………..13 Literature Search…………………………………………13 Data Extraction…………………………………………..14 Analyses………………………………………………….18 Results…………………………………………………………....22 Discussion ...………...…………………………………………..31 Acknowledgments ……………………………………………….37 References………………………………………………………..38 III. Biological control of Eurasian watermilfoil by Euhrychiopsis lecontei: assessing efficacy and timing of sampling……………………………….47 Abstract…………………………………………………………..47
    [Show full text]
  • Order Family Subfamily Genus Species Subspecies Author Year Series Region Units Lepidoptera Crambidae Acentropinae Acentria Ephe
    Order Family Subfamily Genus species subspecies author year series region units Lepidoptera Crambidae Acentropinae Acentria ephemerella (Denis & Schiffermüller) 1C, 1D Nearctic, Palearctic trays Lepidoptera Crambidae Acentropinae Anydraula glycerialis (Walker) 1D Australasian trays Lepidoptera Crambidae Acentropinae Argyractis berthalis (Schaus) 1C Neotropical trays Lepidoptera Crambidae Acentropinae Argyractis dodalis Schaus 1B Neotropical trays Lepidoptera Crambidae Acentropinae Argyractis elphegalis (Schaus) 1B Neotropical trays Lepidoptera Crambidae Acentropinae Argyractis flavalis (Warren) 1B Neotropical trays Lepidoptera Crambidae Acentropinae Argyractis iasusalis (Walker) 1D Neotropical trays Lepidoptera Crambidae Acentropinae Argyractis paulalis (Schaus) 1D Neotropical trays Lepidoptera Crambidae Acentropinae Argyractis sp. 1C, 1D Neotropical trays Lepidoptera Crambidae Acentropinae Argyractis tetropalis Hampson 1D African trays Lepidoptera Crambidae Acentropinae Argyractis triopalis Hampson 1D African trays Lepidoptera Crambidae Acentropinae Argyractoides catenalis (Guenée 1D Neotropical trays Lepidoptera Crambidae Acentropinae Argyractoides chalcistis (Dognin) 1D Neotropical trays Lepidoptera Crambidae Acentropinae Argyractoides gontranalis (Schaus) 1D Neotropical trays Lepidoptera Crambidae Acentropinae Aulacodes acroperalis Hampson 1D Australasian trays Lepidoptera Crambidae Acentropinae Aulacodes adiantealis (Walker) 1D Neotropical trays Lepidoptera Crambidae Acentropinae Aulacodes aechmialis Guenée 1D Neotropical trays Lepidoptera
    [Show full text]
  • Diatraea Lineolata (Walker)
    Keys About Fact Sheets Glossary Larval Morphology References << Previous fact sheet Next fact sheet >> CRAMBIDAE - Diatraea lineolata (Walker) Taxonomy Click here to download this Fact Sheet as a printable PDF Pyraloidea: Crambidae: Crambinae: Diatraea lineolata (Walker) Common names: Neotropical cornstalk borer Synonyms: Chilo culmicolellus, Chilo neuricellus, Diatraea pallidostricta Larval diagnosis (Summary) Mandible with small inner tooth (notch) Fig. 1: Late instar, lateral view Bisetose SV group on the thorax Crochets in a triordinal circle Paraproct setae are never more than half as long as SV1 Color is variable; pinacula are pigmented in non-diapausing larvae and pale in diapausing larvae Found on corn Fig. 2: Late instar, lateral view Host/origin information The majority (>97%) of interception records are from Mexico on corn. Origin Host(s) Mexico Zea mays Fig. 3: Late instar, lateral view Recorded distribution Diatraea lineolata occurs from south Texas to Mexico, Central America, and northern South America. There are also records from parts of the Caribbean (Rodriguez del Bosque et al. 1988). Identifcation authority (Summary) Identification of D. lineolata is difficult because of numerous sibling species. In most cases, a genus-level identification is more accurate. A species-level identification is possible if the larva is Fig. 4: Thorax with bisetose SV group from certain portions of its known distribution and is associated with corn. See the Detailed Information page for information on other Diatraea species. Pest characterization (Based on Cavey 2001, Rodriguez del Bosque et al. 1988) Taxonomy: Medium. Species-level identification is sometimes possible. Distribution: High. Diatraea lineolata is present in the Rio Grande Valley of Texas.
    [Show full text]
  • Mexican Rice Borer, Eoreuma Loftini (Dyar) (Lepidoptera: Crambidae: Crambinae) in Florida Florida Department of Agriculture
    FDACS-P-01827 Florida Department of Agriculture and Consumer Services, Division of Plant Industry Mexican Rice Borer, Eoreuma loftini (Dyar) (Lepidoptera: Crambidae: Crambinae) in Florida James E. Hayden, [email protected], Taxonomic Entomologist, Florida Department of Agriculture and Consumer Services, Division of Plant Industry INTRODUCTION: Eoreuma loftini (Dyar), the Mexican rice borer (MRB), is a major pest of sugarcane, rice, and other grass crops in Mexico, Texas and Louisiana. On 23 March 2012, a single male specimen was collected in Goethe State Forest (Levy County), a new state record. It was caught at a mercury vapor light during a general survey and was identified by dissection on 14 July. The flatwoods habitat is not usual for the moth, although suitable host plants occur in the vicinity. The extent of the population is not currently known. DISTRIBUTION: The moth is native to Mexico and historically in southwestern deserts. In the 20th Century, it spread into the Lower Rio Grande Valley, then southern Texas by 1980, where it displaced the sugarcane borer, Diatraea saccharalis (F.), as the dominant pest of sugarcane. The population had spread to southwestern Louisiana in late 2008. The moth is mainly subtropical, but it can tolerate a few days of below-freezing temperature. IDENTIFICATION: Adult moths are about 1.2 cm (0.5 inch) long and are drab beige with almost no pattern. The forewings have a small black central dot and two faint, blackish longitudinal streaks (Fig. 1). The mouthparts are long, and the forehead is slightly conical, visible only under magnification (Fig. 2). However, many related grass borers share some of these characters, so positive identification requires dissection (Fig.
    [Show full text]
  • Chilo Suppressalis (Walker)
    Asiatic Rice Borer Screening Aid Chilo suppressalis (Walker) Todd M. Gilligan1 and Steven C. Passoa2 1) Identification Technology Program (ITP) / Colorado State University, USDA-APHIS-PPQ-Science & Technology (S&T), 2301 Research Boulevard, Suite 108, Fort Collins, Colorado 80526 U.S.A. (Email: [email protected]) 2) USDA-APHIS-PPQ, The Ohio State University and USDA Forest Service Northern Research Station, 1315 Kinnear Road, Columbus, Ohio 43212 U.S.A. (Email: [email protected]) This CAPS (Cooperative Agricultural Pest Survey) screening aid produced for and distributed by: Version 2.0 USDA-APHIS-PPQ National Identification Services (NIS) 9 Jul 2014 This and other identification resources are available at: http://caps.ceris.purdue.edu/taxonomic_services The Asiatic rice borer, Chilo suppressalis (Walker), is one of the most important pests of rice in East Asia, India, and Indonesia; it has also been introduced to Spain and Hawaii. Larvae cause serious damage to rice plants by boring into the leaf sheath during the vegetative growth stage (causing dead heart) or by feeding on internal tissue during the reproductive growth stage (causing white head). Feeding by C. suppressalis can result in significant reduction in yields or destruction of the entire crop. Larvae also feed on other economically important plants such as maize, sorghum, and sugar-cane. This species is also referred to as the striped stem borer. Chilo suppressalis is a member of the Crambinae (Crambidae), a large subfamily of moths formally in the Pyralidae that contains many pest species. Chilo consists of more than 40 described species, but only four are present in North America.
    [Show full text]
  • Phylogeny, Character Evolution and Species Diversity in Crambinae, Heliothelinae and Scopariinae
    Phylogeny, character evolution and species diversity in Crambinae, Heliothelinae and Scopariinae DISSERTATION zur Erlangung des akademischen Grades DOCTOR RERUM NATURALIUM (Dr. rer. nat.) vorgelegt dem Bereich Mathematik und Naturwissenschaften der Technischen Universit¨at Dresden von M. Sc. Th´eo Antonin Baptiste L´eger geboren am 02.01.1989 in Lausanne, Schweiz eingereicht am 10. Januar 2020 Die Dissertation wurde in der Zeit von 09/2014 bis 12/2019 an den Senckenberg Naturhistorischen Sammlungen Dresden angefertigt. ii Charles Darwin, letter to T. H. Huxley, 26 September 1857 Darwin Correspondence Project, “Letter no. 2143”, https://www.darwinproject.ac.uk/letter/DCP-LETT-2143.xml 1. Gutachter 2. Gutachter Prof. Dr. Christoph Neinhuis Prof. Dr. Niklas Wahlberg Lehrstuhl f¨ur Botanik, Systematic Biology Group Fakult¨at Mathematik und Faculty of Science Naturwissenschaften Lund University Technische Universit¨at Dresden S¨olvegatan 37, Lund Dresden, Deutschland Schweden Declaration Erkl¨arung gem¨aß § 5.1.5 der Promotionsordnung Hiermit versichere ich, dass ich die vorliegende Arbeit ohne unzul¨assigeHilfe Dritter und ohne Benutzung anderer als der angegebenen Hilfsmittel angefertigt habe; die aus fremden Quellen direkt oder indirektubernommenen ¨ Gedanken sind als solche kenntlich gemacht. Die Arbeit wurde bisher weder im Inland noch im Ausland in gleicher oder ¨ahnlicher Form einer anderen Pr¨ufungsbeh¨orde vorgelegt. Berlin, 14. Januar 2020 Th´eo L´eger iii iv Acknowledgements This work would not have been possible without the help and support from various people. I want to express my sincere gratitude to Matthias Nuss and Bernard Landry for introducing me to the fabulous group that represent Pyraloidea and to the thrilling field of research that is systematics.
    [Show full text]
  • The Species Richness of Lepidoptera in a Fragmented Landscape: a Supplement to the Checklist of Moths of Butler County, Ohio
    The Great Lakes Entomologist Volume 34 Number 1 - Spring/Summer 2001 Number 1 - Article 12 Spring/Summer 2001 April 2001 The Species Richness of Lepidoptera in a Fragmented Landscape: A Supplement to the Checklist of Moths of Butler County, Ohio Keith S. Summerville Miami University Thomas O. Crist Miami University Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Summerville, Keith S. and Crist, Thomas O. 2001. "The Species Richness of Lepidoptera in a Fragmented Landscape: A Supplement to the Checklist of Moths of Butler County, Ohio," The Great Lakes Entomologist, vol 34 (1) Available at: https://scholar.valpo.edu/tgle/vol34/iss1/12 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. Summerville and Crist: The Species Richness of Lepidoptera in a Fragmented Landscape: A 2001 THE GREAT LAKES ENTOMOLOGIST 93 THE SPECIES RICHNESS OF lEPIDOPTERA IN A FRAGMENTED LANDSCAPE: A SUPPLEMENT TO THE CHECKLIST OF MOTHS OF BUTlER COUNTY, OHIO Keith S. Summerville 1 and Thomas O. Crist1 ABSTRACT Land conversion for agriculture or urban expansion has fragmented the midwestern landscape and isolated native biotas in remnant habitat patches. Identification of priority renmants to be targeted for conservation, however, requires an understanding of the species diversity and distributions in such fragmented landscapes. During a 3-year inventory, we estimated the species richness of Lepidoptera in forests and old fields within an agricultural region of southwest Ohio, Butler County.
    [Show full text]