Arthropod Genomics Symposium Platform/Oral Presentations
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Redalyc.Nidification of Polybia Rejecta (Hymenoptera: Vespidae)
Biota Neotropica ISSN: 1676-0611 [email protected] Instituto Virtual da Biodiversidade Brasil Magalhães de Souza, Marcos; Porfiro Pires, Epifânio; Prezoto, Fábio Nidification of Polybia rejecta (Hymenoptera: Vespidae) associated to Azteca chartifex (Hymenoptera: Formicidae) in a fragment of Atlantic Forest, in the state of Minas Gerais, southeastern Brazil Biota Neotropica, vol. 13, núm. 3, julio-septiembre, 2013, pp. 390-392 Instituto Virtual da Biodiversidade Campinas, Brasil Available in: http://www.redalyc.org/articulo.oa?id=199128991038 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Biota Neotrop., vol. 13, no. 3 Nidification of Polybia rejecta (Hymenoptera: Vespidae) associated to Azteca chartifex (Hymenoptera: Formicidae) in a fragment of Atlantic Forest, in the state of Minas Gerais, southeastern Brazil Marcos Magalhães de Souza1, Epifânio Porfiro Pires2,4 & Fábio Prezoto3 1Instituto Federal de Educação, Ciência e Tecnologia do Sul de Minas – IFSULDEMINAS, Campus Inconfidentes, CEP 37576-000, Inconfidentes, MG, Brazil 2Departamento de Entomologia, Universidade Federal de Lavras – UFLA, CEP 37200-000, Lavras, MG, Brazil 3Departamento de Zoologia, Universidade Federal de Juiz de Fora – UFJF, CEP 36036-900, Juiz de Fora, MG, Brazil 4Corresponding author: Epifânio Porfiro Pires, e-mail: [email protected] -
Attraction of Apple Maggot Flies (Diptera: Tephritidae) to Synthetic Fruit Volatile Compounds and Food Attractants in Michigan Apple Orchards
The Great Lakes Entomologist Volume 35 Number 1 - Spring/Summer 2002 Number 1 - Article 8 Spring/Summer 2002 April 2002 Attraction of Apple Maggot Flies (Diptera: Tephritidae) to Synthetic Fruit Volatile Compounds and Food Attractants in Michigan Apple Orchards Lukasz L. Stenliski Michigan State University Ocar E. Liburd University of Florida Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Stenliski, Lukasz L. and Liburd, Ocar E. 2002. "Attraction of Apple Maggot Flies (Diptera: Tephritidae) to Synthetic Fruit Volatile Compounds and Food Attractants in Michigan Apple Orchards," The Great Lakes Entomologist, vol 35 (1) Available at: https://scholar.valpo.edu/tgle/vol35/iss1/8 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]. Stenliski and Liburd: Attraction of Apple Maggot Flies (Diptera: Tephritidae) to Synthe 2002 THE GREAT LAKES ENTOMOLOGIST 37 ATTRACTION OF APPLE MAGGOT FLIES (DIPTERA: TEPHRITIDAE) TO SYNTHETIC FRUIT VOLATILE COMPOUNDS AND FOOD ATTRACTANTS IN MICHIGAN APPLE ORCHARDS Lukasz L. Stenliski1 and Ocar E. Liburd2 ABSTRACT The apple maggot, Rhagoletis pomonella (Walsh), is a serious pest of apples in the United States, requiring reliable monitoring and control programs. Various synthetic apple volatile lures with and without protein hydrolysate, ammonium acetate, or ammonium carbonate were evaluated from 1998-2000 for their attractiveness to R. pomonella adults with red sticky-sphere (9 cm diam.) monitoring traps. -
Apple Maggot [Rhagoletis Pomonella (Walsh)]
Published by Utah State University Extension and Utah Plant Pest Diagnostic Laboratory ENT-06-87 November 2013 Apple Maggot [Rhagoletis pomonella (Walsh)] Diane Alston, Entomologist, and Marion Murray, IPM Project Leader Do You Know? • The fruit fly, apple maggot, primarily infests native hawthorn in Utah, but recently has been found in home garden plums. • Apple maggot is a quarantine pest; its presence can restrict export markets for commercial fruit. • Damage occurs from egg-laying punctures and the larva (maggot) developing inside the fruit. • The larva drops to the ground to spend the winter as a pupa in the soil. • Insecticides are currently the most effective con- trol method. • Sanitation, ground barriers under trees (fabric, Fig. 1. Apple maggot adult on plum fruit. Note the F-shaped mulch), and predation by chickens and other banding pattern on the wings.1 fowl can reduce infestations. pple maggot (Order Diptera, Family Tephritidae; Fig. A1) is not currently a pest of commercial orchards in Utah, but it is regulated as a quarantine insect in the state. If it becomes established in commercial fruit production areas, its presence can inflict substantial economic harm through loss of export markets. Infesta- tions cause fruit damage, may increase insecticide use, and can result in subsequent disruption of integrated pest management programs. Fig. 2. Apple maggot larva in a plum fruit. Note the tapered head and dark mouth hooks. This fruit fly is primarily a pest of apples in northeastern home gardens in Salt Lake County. Cultivated fruit is and north central North America, where it historically more likely to be infested if native hawthorn stands are fed on fruit of wild hawthorn. -
A Review of Sampling and Monitoring Methods for Beneficial Arthropods
insects Review A Review of Sampling and Monitoring Methods for Beneficial Arthropods in Agroecosystems Kenneth W. McCravy Department of Biological Sciences, Western Illinois University, 1 University Circle, Macomb, IL 61455, USA; [email protected]; Tel.: +1-309-298-2160 Received: 12 September 2018; Accepted: 19 November 2018; Published: 23 November 2018 Abstract: Beneficial arthropods provide many important ecosystem services. In agroecosystems, pollination and control of crop pests provide benefits worth billions of dollars annually. Effective sampling and monitoring of these beneficial arthropods is essential for ensuring their short- and long-term viability and effectiveness. There are numerous methods available for sampling beneficial arthropods in a variety of habitats, and these methods can vary in efficiency and effectiveness. In this paper I review active and passive sampling methods for non-Apis bees and arthropod natural enemies of agricultural pests, including methods for sampling flying insects, arthropods on vegetation and in soil and litter environments, and estimation of predation and parasitism rates. Sample sizes, lethal sampling, and the potential usefulness of bycatch are also discussed. Keywords: sampling methodology; bee monitoring; beneficial arthropods; natural enemy monitoring; vane traps; Malaise traps; bowl traps; pitfall traps; insect netting; epigeic arthropod sampling 1. Introduction To sustainably use the Earth’s resources for our benefit, it is essential that we understand the ecology of human-altered systems and the organisms that inhabit them. Agroecosystems include agricultural activities plus living and nonliving components that interact with these activities in a variety of ways. Beneficial arthropods, such as pollinators of crops and natural enemies of arthropod pests and weeds, play important roles in the economic and ecological success of agroecosystems. -
Phylogenetic Relationships and Historical Biogeography of Tribes and Genera in the Subfamily Nymphalinae (Lepidoptera: Nymphalidae)
Blackwell Science, LtdOxford, UKBIJBiological Journal of the Linnean Society 0024-4066The Linnean Society of London, 2005? 2005 862 227251 Original Article PHYLOGENY OF NYMPHALINAE N. WAHLBERG ET AL Biological Journal of the Linnean Society, 2005, 86, 227–251. With 5 figures . Phylogenetic relationships and historical biogeography of tribes and genera in the subfamily Nymphalinae (Lepidoptera: Nymphalidae) NIKLAS WAHLBERG1*, ANDREW V. Z. BROWER2 and SÖREN NYLIN1 1Department of Zoology, Stockholm University, S-106 91 Stockholm, Sweden 2Department of Zoology, Oregon State University, Corvallis, Oregon 97331–2907, USA Received 10 January 2004; accepted for publication 12 November 2004 We infer for the first time the phylogenetic relationships of genera and tribes in the ecologically and evolutionarily well-studied subfamily Nymphalinae using DNA sequence data from three genes: 1450 bp of cytochrome oxidase subunit I (COI) (in the mitochondrial genome), 1077 bp of elongation factor 1-alpha (EF1-a) and 400–403 bp of wing- less (both in the nuclear genome). We explore the influence of each gene region on the support given to each node of the most parsimonious tree derived from a combined analysis of all three genes using Partitioned Bremer Support. We also explore the influence of assuming equal weights for all characters in the combined analysis by investigating the stability of clades to different transition/transversion weighting schemes. We find many strongly supported and stable clades in the Nymphalinae. We are also able to identify ‘rogue’ -
Sympatric Ecological Speciation Meets Pyrosequencing: Sampling
Western Washington University Western CEDAR Biology Faculty and Staff ubP lications Biology 12-27-2009 Sympatric Ecological Speciation Meets Pyrosequencing: Sampling the Transcriptome of the Apple Maggot Rhagoletis Pomonella Dietmar Schwarz Western Washington University, [email protected] Hugh M. Robertson Jeffrey L. Feder Kranthi Varala Matthew E. Hudson See next page for additional authors Follow this and additional works at: https://cedar.wwu.edu/biology_facpubs Part of the Biology Commons Recommended Citation Schwarz, Dietmar; Robertson, Hugh M.; Feder, Jeffrey L.; Varala, Kranthi; Hudson, Matthew E.; Ragland, Gregory J.; Hahn, Daniel A.; and Berlocher, Stewart H., "Sympatric Ecological Speciation Meets Pyrosequencing: Sampling the Transcriptome of the Apple Maggot Rhagoletis Pomonella" (2009). Biology Faculty and Staff Publications. 25. https://cedar.wwu.edu/biology_facpubs/25 This Article is brought to you for free and open access by the Biology at Western CEDAR. It has been accepted for inclusion in Biology Faculty and Staff ubP lications by an authorized administrator of Western CEDAR. For more information, please contact [email protected]. Authors Dietmar Schwarz, Hugh M. Robertson, Jeffrey L. Feder, Kranthi Varala, Matthew E. Hudson, Gregory J. Ragland, Daniel A. Hahn, and Stewart H. Berlocher This article is available at Western CEDAR: https://cedar.wwu.edu/biology_facpubs/25 BMC Genomics BioMed Central Research article Open Access Sympatric ecological speciation meets pyrosequencing: sampling the transcriptome of the apple maggot Rhagoletis pomonella Dietmar Schwarz*1,5, Hugh M Robertson1, Jeffrey L Feder2, Kranthi Varala3, Matthew E Hudson3, Gregory J Ragland4, Daniel A Hahn4 and Stewart H Berlocher1 Address: 1Department of Entomology, University of Illinois, 320 Morrill Hall, 505 S. -
Hymenoptera: Formicidae)
Myrmecological News 20 25-36 Online Earlier, for print 2014 The evolution and functional morphology of trap-jaw ants (Hymenoptera: Formicidae) Fredrick J. LARABEE & Andrew V. SUAREZ Abstract We review the biology of trap-jaw ants whose highly specialized mandibles generate extreme speeds and forces for predation and defense. Trap-jaw ants are characterized by elongated, power-amplified mandibles and use a combination of latches and springs to generate some of the fastest animal movements ever recorded. Remarkably, trap jaws have evolved at least four times in three subfamilies of ants. In this review, we discuss what is currently known about the evolution, morphology, kinematics, and behavior of trap-jaw ants, with special attention to the similarities and key dif- ferences among the independent lineages. We also highlight gaps in our knowledge and provide suggestions for future research on this notable group of ants. Key words: Review, trap-jaw ants, functional morphology, biomechanics, Odontomachus, Anochetus, Myrmoteras, Dacetini. Myrmecol. News 20: 25-36 (online xxx 2014) ISSN 1994-4136 (print), ISSN 1997-3500 (online) Received 2 September 2013; revision received 17 December 2013; accepted 22 January 2014 Subject Editor: Herbert Zettel Fredrick J. Larabee (contact author), Department of Entomology, University of Illinois, Urbana-Champaign, 320 Morrill Hall, 505 S. Goodwin Ave., Urbana, IL 61801, USA; Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013-7012, USA. E-mail: [email protected] Andrew V. Suarez, Department of Entomology and Program in Ecology, Evolution and Conservation Biology, Univer- sity of Illinois, Urbana-Champaign, 320 Morrill Hall, 505 S. -
For Submission As a Note Green Anole (Anolis Carolinensis) Eggs
For submission as a Note Green Anole (Anolis carolinensis) Eggs Associated with Nest Chambers of the Trap Jaw Ant, Odontomachus brunneus Christina L. Kwapich1 1Department of Biological Sciences, University of Massachusetts Lowell One University Ave., Lowell, Massachusetts, USA [email protected] Abstract Vertebrates occasionally deposit eggs in ant nests, but these associations are largely restricted to neotropical fungus farming ants in the tribe Attini. The subterranean chambers of ponerine ants have not previously been reported as nesting sites for squamates. The current study reports the occurrence of Green Anole (Anolis carolinensis) eggs and hatchlings in a nest of the trap jaw ant, Odontomachus brunneus. Hatching rates suggest that O. brunneus nests may be used communally by multiple females, which share spatial resources with another recently introduced Anolis species in their native range. This nesting strategy is placed in the context of known associations between frogs, snakes, legless worm lizards and ants. Introduction Subterranean ant nests are an attractive resource for vertebrates seeking well-defended cavities for their eggs. To access an ant nest, trespassers must work quickly or rely on adaptations that allow them to overcome the strict odor-recognition systems of ants. For example the myrmecophilous frog, Lithodytes lineatus, bears a chemical disguise that permits it to mate and deposit eggs deep inside the nests of the leafcutter ant, Atta cephalotes, without being bitten or harassed. Tadpoles inside nests enjoy the same physical and behavioral protection as the ants’ own brood, in a carefully controlled microclimate (de Lima Barros et al. 2016, Schlüter et al. 2009, Schlüter and Regös 1981, Schlüter and Regös 2005). -
Azteca Ants Maintain Unique Microbiomes Across Functionally
Azteca ants maintain unique microbiomes royalsocietypublishing.org/journal/rspb across functionally distinct nest chambers Jane M. Lucas1, Anne A. Madden2, Clint A. Penick3, Mary Jane Epps5, Peter R. Marting4, Julia L. Stevens6, Daniel J. Fergus2, Robert R. Dunn2,7 Research and Emily K. Meineke8 1 Cite this article: Lucas JM, Madden AA, Department of Soil and Water Systems, University of Idaho, Moscow, ID 83844, USA 2Department of Applied Ecology, North Carolina State University, Raleigh, NC 27695, USA Penick CA, Epps MJ, Marting PR, Stevens JL, 3The Biomimicry Center, and 4School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA Fergus DJ, Dunn RR, Meineke EK. 2019 Azteca 5Department of Biology, Mary Baldwin University, Staunton, VA 24401, USA 6 ants maintain unique microbiomes across Bayer Crop Science Division, Saint Louis, MO 63146, USA 7Natural History Museum, University of Copenhagen, DK-2100 Copenhagen, Denmark functionally distinct nest chambers. 8Department of Organismic and Evolutionary Biology, Harvard University Herbaria, Cambridge, MA 02138, USA Proc. R. Soc. B 286: 20191026. JML, 0000-0002-3931-1864; AAM, 0000-0002-7263-5713; CAP, 0000-0002-5368-507X; http://dx.doi.org/10.1098/rspb.2019.1026 RRD, 0000-0002-6030-4837 The microbiome of built structures has considerable influence over an inhabitant’s well-being, yet the vast majority of research has focused on Received: 2 May 2019 human-built structures. Ants are well-known architects, capable of con- Accepted: 12 July 2019 structing elaborate dwellings, the microbiome of which is underexplored. Here, we explore the bacterial and fungal microbiomes in functionally dis- tinct chambers within and outside the nests of Azteca alfari ants in Cecropia peltata trees. -
The Encodedb Portal: Simplified Access to ENCODE Consortium Data Laura L
Downloaded from genome.cshlp.org on September 30, 2021 - Published by Cold Spring Harbor Laboratory Press Resource The ENCODEdb portal: Simplified access to ENCODE Consortium data Laura L. Elnitski, Prachi Shah, R. Travis Moreland, Lowell Umayam, Tyra G. Wolfsberg, and Andreas D. Baxevanis1 Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA The Encyclopedia of DNA Elements (ENCODE) project aims to identify and characterize all functional elements in a representative chromosomal sample comprising 1% of the human genome. Data generated by members of The ENCODE Project Consortium are housed in a number of public databases, such as the UCSC Genome Browser, NCBI’s Gene Expression Omnibus (GEO), and EBI’s ArrayExpress. As such, it is often difficult for biologists to gather all of the ENCODE data from a particular genomic region of interest and integrate them with relevant information found in other public databases. The ENCODEdb portal was developed to address this problem. ENCODEdb provides a unified, single point-of-access to data generated by the ENCODE Consortium, as well as to data from other source databases that lie within ENCODE regions; this provides the user a complete view of all known data in a particular region of interest. ENCODEdb Genomic Context searches allow for the retrieval of information on functional elements annotated within ENCODE regions, including mRNA, EST, and STS sequences; single nucleotide polymorphisms, and UniGene clusters. Information is also retrieved from GEO, OMIM, and major genome sequence browsers. ENCODEdb Consortium Data searches allow users to perform compound queries on array-based ENCODE data available both from GEO and from the UCSC Genome Browser. -
Genomes of the Hymenoptera Michael G
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital Repository @ Iowa State University Ecology, Evolution and Organismal Biology Ecology, Evolution and Organismal Biology Publications 2-2018 Genomes of the Hymenoptera Michael G. Branstetter U.S. Department of Agriculture Anna K. Childers U.S. Department of Agriculture Diana Cox-Foster U.S. Department of Agriculture Keith R. Hopper U.S. Department of Agriculture Karen M. Kapheim Utah State University See next page for additional authors Follow this and additional works at: https://lib.dr.iastate.edu/eeob_ag_pubs Part of the Behavior and Ethology Commons, Entomology Commons, and the Genetics and Genomics Commons The ompc lete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ eeob_ag_pubs/269. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Ecology, Evolution and Organismal Biology at Iowa State University Digital Repository. It has been accepted for inclusion in Ecology, Evolution and Organismal Biology Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Genomes of the Hymenoptera Abstract Hymenoptera is the second-most sequenced arthropod order, with 52 publically archived genomes (71 with ants, reviewed elsewhere), however these genomes do not capture the breadth of this very diverse order (Figure 1, Table 1). These sequenced genomes represent only 15 of the 97 extant families. Although at least 55 other genomes are in progress in an additional 11 families (see Table 2), stinging wasps represent 35 (67%) of the available and 42 (76%) of the in progress genomes. -
Differential Gene Expression Profiling in Bed Bug (Cimex Lectularius L.) Fed on Ibuprofen and Caffeine in Reconstituted Human Blood Ralph B
Herpe y & tolo og g l y: o C th i u Narain et al., Entomol Ornithol Herpetol 2015, 4:3 n r r r e O n , t y R g DOI: 10.4172/2161-0983.1000160 e o l s o e a m r o c t h n E Entomology, Ornithology & Herpetology ISSN: 2161-0983 ResearchResearch Article Article OpenOpen Access Access Differential Gene Expression Profiling in Bed Bug (Cimex Lectularius L.) Fed on Ibuprofen and Caffeine in Reconstituted Human Blood Ralph B. Narain, Haichuan Wang and Shripat T. Kamble* Department of Entomology, University of Nebraska, Lincoln, NE 68583, USA Abstract The recent resurgence of the common bed bug (Cimex lectularius L.) infestations worldwide has created a need for renewed research on biology, behavior, population genetics and management practices. Humans serve as exclusive hosts to bed bugs in urban environments. Since a majority of humans consume Ibuprofen (as pain medication) and caffeine (in coffee and other soft drinks) so bug bugs subsequently acquire Ibuprofen and caffeine through blood feeding. However, the effect of these chemicals at genetic level in bed bug is unknown. Therefore, this research was conducted to determine differential gene expression in bed bugs using RNA-Seq analysis at dosages of 200 ppm Ibuprofen and 40 ppm caffeine incorporated into reconstituted human blood and compared against the control. Total RNA was extracted from a single bed bug per replication per treatment and sequenced. Read counts obtained were analyzed using Bioconductor software programs to identify differentially expressed genes, which were then searched against the non-redundant (nr) protein database of National Center for Biotechnology Information (NCBI).