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Type Material of a Pine Web-Spinning Sawfly, Acantholyda Sasakii (Yano
Bull. Natl. Mus. Nat. Sci., Ser. A, 39(3), pp. 131–132, August 22, 2013 Type Material of a Pine Web-spinning Sawfly, Acantholyda sasakii (Yano, 1916) (Hymenoptera, Pamphiliidae) Akihiko Shinohara Department of Zoology, National Museum of Nature and Science, 4–1–1 Amakubo, Tsukuba, Ibaraki, 305–0005 Japan E-mail: [email protected] (Received 1 June 2013; accepted 12 July 2013) Abstract The type material of Acantholyda sasakii (Yano, 1916), once thought to be lost, has been found in the collection of the University Museum, the University of Tokyo, Tokyo. A lectotype is designated for the taxon. An examination of the lectotype has shown that the current interpretation of the taxon is correct. Key words : Hymenoptera, Pamphiliidae, Acantholyda sasakii, lectotype designation. Acantholyda sasakii (Yano, 1916) is a conifer- 1918] from Europe and named it “Lgda [sic] feeding, web-spinning sawfly occurring in Hon- sasakii”. Takeuchi (1930) transferred it to the shu, Japan (Shinohara, 1995, 2001). Sasaki genus Acantholyda Costa, 1894. Although Sasa- (1901) first described this species as “Tenthredo ki’s original material has never been studied, as it pratensis, F. var.?” without giving the number of was thought to be lost (Shinohara, 1995), the specimens he examined. Yano (1916) pointed out species is quite characteristic and easily recog- that Sasaki’s species differed from “Tenthredo nized by the features given by Sasaki (1901). pratensis F.” [=Tenthredo stellata Christ, =Acan- Chûjirô Sasaki (1857–1938) was a professor tholyda (Itycorsia) posticalis pinivora Enslin, of Entomology at the College of Agriculture, Fig. 1. Lectotype of Lyda sasakii Yano, 1916. 132 Akihiko Shinohara Tokyo Imperial University (currently the Univer- of the antennae and the right fore tibia and tarsus sity of Tokyo), and his insect collection is sup- are missing, and the left wings are detached from posed to have been deposited in the college. -
Towards Simultaneous Analysis of Morphological and Molecular Data in Hymenoptera
Towards simultaneous analysis of morphological and molecular data in Hymenoptera JAMES M. CARPENTER &WARD C. WHEELER Accepted 5 January 1999 Carpenter, J. M. & W. C. Wheeler. (1999). Towards simultaneous analysis of molecular and morphological data in Hymenoptera. Ð Zoologica Scripta 28, 251±260. Principles and methods of simultaneous analysis in cladistics are reviewed, and the first, preliminary, analysis of combined molecular and morphological data on higher level relationships in Hymenoptera is presented to exemplify these principles. The morphological data from Ronquist et al. (in press) matrix, derived from the character diagnoses of the phylogenetic tree of Rasnitsyn (1988), are combined with new molecular data for representatives of 10 superfamilies of Hymenoptera by means of optimization alignment. The resulting cladogram supports Apocrita and Aculeata as groups, and the superfamly Chrysidoidea, but not Chalcidoidea, Evanioidea, Vespoidea and Apoidea. James M. Carpenter, Department of Entomology, and Ward C. Wheeler, Department of Invertebrates, American Museum of Natural History, Central Park West at 79th Street, New York, NY 10024, U SA. E-mail: [email protected] Introduction of consensus techniques to the results of independent Investigation of the higher-level phylogeny of Hymenoptera analysis of multiple data sets, as for example in so-called is at a very early stage. Although cladistic analysis was ®rst `phylogenetic supertrees' (Sanderson et al. 1998), does not applied more than 30 years ago, in an investigation of the measure the strength of evidence supporting results from ovipositor by Oeser (1961), a comprehensive analysis of all the different data sources Ð in addition to other draw- the major lineages remains to be done. -
Pine Sawflies, Neodiprion Spp. (Insecta: Hymenoptera: Diprionidae)1 Wayne N
EENY317 Pine Sawflies, Neodiprion spp. (Insecta: Hymenoptera: Diprionidae)1 Wayne N. Dixon2 Introduction Pine sawfly larvae, Neodiprion spp., are the most common defoliating insects of pine trees, Pinus spp., in Florida. Sawfly infestations can cause growth loss and mortality, especially when followed by secondary attack by bark and wood-boring beetles (Coleoptera: Buprestidae, Cerambycidae, Scolytidae). Trees of all ages are susceptible to sawfly defoliation (Barnard and Dixon 1983; Coppel and Benjamin 1965). Distribution Neodiprion spp. are indigenous to Florida. Host tree specificity and location will bear on sawfly distribution statewide. Description Six species are covered here so there is some variation in appearance. However, an adult female has a length of 8 to 10 mm, with narrow antennae on the head and a stout and Figure 1. Larvae of the blackheaded pine sawfly, Neodiprion excitans thick-waisted body. This is unlike most Hymenopteran Rohwer, on Pinus sp. Credits: Arnold T. Drooz, USDA Forest Service; www.forestryimages.org insects which have the thinner, wasp-like waist. The background color varies from light to dark brown, with Adult yellow-red-white markings common. The two pairs of The adult male has a length of 5 to 7 mm. The male has wings are clear to light brown with prominent veins. broad, feathery antennae on the head with a slender, thick- waisted body. It generally has brown to black color wings, similar to the female. 1. This document is EENY317 (originally published as DPI Entomology Circular No. 258), one of a series of the Department of Entomology and Nematology, UF/IFAS Extension. Original publication date January 2004. -
Supplementary Materials Neodiprion Sawflies
Supplementary Materials Neodiprion sawflies: life history description and utility as a model for parent-offspring conflict To provide context for our comparative analysis of Neodiprion clutch-size traits, we provide relevant life history details (reviewed in Coppel and Benjamin 1965; Knerer and Atwood 1973; Wilson et al. 1992; Knerer 1993). Adult females emerge from cocoons with a full complement of mature eggs, find a suitable host, and attract males via a powerful pheromone. Shortly after mating, females use their saw-like ovipositors to embed their eggs within pine needles. While females of some species tend to lay their full complement of eggs on a single branch terminus, females of other species seek out multiple branches or trees for oviposition. Overall, female oviposition behavior is highly species-specific and, in some cases, diagnostic (Ghent 1959). Adult Neodiprion are non-feeding and short-lived (~2-4 days), dying soon after mating and oviposition. After hatching from eggs, Neodiprion larvae of many species form feeding aggregations that remain intact to varying degrees across 4-7 feeding instars, depending on the sex and the species. As larvae defoliate pine branches, they migrate to new branches and sometimes to new host trees (Benjamin 1955, Smirnoff 1960). During these migrations, colonies may undergo fission and fusion events (Codella and Raffa 1993, Codella and Raffa 1995, Costa and Loque 2001). Thus, while initial colony size corresponds closely to egg-clutch size, larvae are highly mobile and their dispersal behavior has the potential to substantially alter colony size (Codella and Raffa 1995). Beyond having a variable and well-documented natural history, Neodiprion provides an excellent test case for examining coevolution of female egg-laying and larval grouping behaviors because, as is likely the case for many insects, feeding in groups could confer both costs and benefits to the larvae (Codella and Raffa 1995, Heitland and Pschorn-Walcher 1993). -
Hymenoptera: Chalcidoidea) of Morocco
Graellsia, 77(1): e139 enero-junio 2021 ISSN-L: 0367-5041 https://doi.org/10.3989/graellsia.2021.v77.301 ANNOTATED CHECK-LIST OF PTEROMALIDAE (HYMENOPTERA: CHALCIDOIDEA) OF MOROCCO. PART II Khadija Kissayi1,*, Mircea-Dan Mitroiu2 & Latifa Rohi3 1 National School of Forestry, Department of Forest Development, B.P. 511, Avenue Moulay Youssef, Tabriquet, 11 000, Salé, Morocco. Email: [email protected] – ORCID iD: https://orcid.org/0000-0003-3494-2250 2 Alexandru Ioan Cuza, University of Iaşi, Faculty of Biology, Research Group on Invertebrate Diversity and Phylogenetics, Bd. Carol I 20A, 700 505, Iaşi, Romania. Email: [email protected] – ORCID iD: https://orcid.org/0000-0003-1368-7721 3 University Hassan II, Faculty of Sciences Ben M’sik, Laboratory of ecology and environment, Avenue Driss El Harti, B.P. 7955, Casablanca, 20 800 Morocco. Email: [email protected] / or [email protected] – ORCID iD: https://orcid.org/0000-0002-4180-1117 * Corresponding author: [email protected] ABSTRACT In this second part, we present the subfamily Pteromalinae in Morocco, which includes 86 species belonging to 50 genera. Fifteen genera and 37 species are listed for the first time in the Moroccan fauna, among which 9 have been newly identified, 24 have been found in the bibliography and 4 deposited in natural history museums. An updated list of Moroccan species is given, including their distribution by regions, their general distribution and their hosts. Keywords: Pteromalinae; distribution; hosts; new record; Morocco; Palaearctic Region. RESUMEN Lista comentada de Pteromalidae (Hymenoptera: Chalcidoidea) de Marruecos. Parte II En esta segunda parte, presentamos la subfamilia Pteromalinae en Marruecos, que incluye 86 especies pertenecientes a 50 géneros. -
2015 Forest Health Highlights Michigan Department of Natural Resources Acknowledgments
2015 Forest Health Highlights Michigan Department of Natural Resources Acknowledgments Forest Health Highlights is a summary of the condition of Michigan’s forests during 2015 and the work done to preserve and protect them by Forest Resources Division, Department of Natural Resources, www.michigan.gov/foresthealth. Written by Michigan Department of Natural Resources Forest Resources Division Michigan Department of Agriculture and Rural Development Michigan State University Department of Forestry and the Department of Entomology United States Department of Agriculture Forest Service Photographs and design by Michigan Department of Natural Resources Forest Resources Division United States Department of Agriculture Forest Service Michigan Department of Agriculture & Rural Development Michigan State University Maps and other information provided by Michigan Department of Agriculture and Rural Development United States Department of Agriculture Forest Service and Animal and Plant Health Inspection Service Michigan State University Extension Cover photo: The redheaded pine sawfly, Neodiprion lecontei, is native to Michigan and much of eastern North America. The larvae feed in colonies and consume both new and old foliage. During outbreaks, multiple colonies can attack young trees and cause complete defoliation and tree mortality. The preferred hosts in Michigan are jack pine and red pine. Young plantations less than 15 feet in height are at greatest risk. Photo by Michigan Department of Natural Resources forest health technician Scott Lint. -
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. -
Insect Classification Standards 2020
RECOMMENDED INSECT CLASSIFICATION FOR UGA ENTOMOLOGY CLASSES (2020) In an effort to standardize the hexapod classification systems being taught to our students by our faculty in multiple courses across three UGA campuses, I recommend that the Entomology Department adopts the basic system presented in the following textbook: Triplehorn, C.A. and N.F. Johnson. 2005. Borror and DeLong’s Introduction to the Study of Insects. 7th ed. Thomson Brooks/Cole, Belmont CA, 864 pp. This book was chosen for a variety of reasons. It is widely used in the U.S. as the textbook for Insect Taxonomy classes, including our class at UGA. It focuses on North American taxa. The authors were cautious, presenting changes only after they have been widely accepted by the taxonomic community. Below is an annotated summary of the T&J (2005) classification. Some of the more familiar taxa above the ordinal level are given in caps. Some of the more important and familiar suborders and families are indented and listed beneath each order. Note that this is neither an exhaustive nor representative list of suborders and families. It was provided simply to clarify which taxa are impacted by some of more important classification changes. Please consult T&J (2005) for information about taxa that are not listed below. Unfortunately, T&J (2005) is now badly outdated with respect to some significant classification changes. Therefore, in the classification standard provided below, some well corroborated and broadly accepted updates have been made to their classification scheme. Feel free to contact me if you have any questions about this classification. -
Redheaded Pine Sawfly Neodiprion Lecontei (Fitch)1 Sara Deberry2
EENY488 doi.org/10.32473/edis-in329-2000 Redheaded Pine Sawfly Neodiprion lecontei (Fitch)1 Sara DeBerry2 The Featured Creatures collection provides in-depth profiles of insects, nematodes, arachnids and other organisms relevant to Florida. These profiles are intended for the use of interested laypersons with some knowledge of biology as well as academic audiences. Introduction The redheaded pine sawfly, Neodiprion lecontei (Fitch), is one of numerous sawfly species (including 35 species in the genus Neodiprion) native to the United States and Canada (Arnett 2000) inhabiting mainly pine stands. The ovipositor of all adult female sawflies is saw-like, and is likely where the common name for this group (suborder) originated (PADCNR 2010). Neodiprion lecontei is an important defoliator of com- mercially grown pine, as the preferred feeding conditions for sawfly larvae are enhanced in monocultures of shortleaf, loblolly, and slash pine, all of which are commonly culti- vated in the southern United States. Figure 1. Adult female redheaded pine sawfly, Neodiprion lecontei (Fitch). Distribution Credits: Lacy L. Hyche, Auburn University, www.forestryimages.org Numerous sawfly species are found in North America. The redheaded pine sawfly is native to the United States and Description found primarily east of the Great Plains (Wilson 1978), Adults north into Canada, and south into Florida. Adult sawflies have a broad “waist,” in contrast with many other hymenopterans, and have two pairs of membranous wings. Adults are 0.5–0.85 cm (1/5–1/3 inch) in length, with the females being approximately two-thirds larger than 1. This document is EENY488, one of a series of the Entomology and Nematology Department, UF/IFAS Extension. -
Baculovirus Enhancins and Their Role in Viral Pathogenicity
9 Baculovirus Enhancins and Their Role in Viral Pathogenicity James M. Slavicek USDA Forest Service USA 1. Introduction Baculoviruses are a large group of viruses pathogenic to arthropods, primarily insects from the order Lepidoptera and also insects in the orders Hymenoptera and Diptera (Moscardi 1999; Herniou & Jehle, 2007). Baculoviruses have been used to control insect pests on agricultural crops and forests around the world (Moscardi, 1999; Szewczk et al., 2006, 2009; Erlandson 2008). Efforts have been ongoing for the last two decades to develop strains of baculoviruses with greater potency or other attributes to decrease the cost of their use through a lower cost of production or application. Early efforts focused on the insertion of foreign genes into the genomes of baculoviruses that would increase viral killing speed for use to control agricultural insect pests (Black et al., 1997; Bonning & Hammock, 1996). More recently, research efforts have focused on viral genes that are involved in the initial and early processes of infection and host factors that impede successful infection (Rohrmann, 2011). The enhancins are proteins produced by some baculoviruses that are involved in one of the earliest events of host infection. This article provides a review of baculovirus enhancins and their role in the earliest phases of viral infection. 2. Lepidopteran specific baculoviruses The Baculoviridae are divided into four genera: the Alphabaculovirus (lepidopteran-specific nucleopolyhedroviruses, NPV), Betabaculovirus (lepidopteran specific Granuloviruses, GV), Gammabaculovirus (hymenopteran-specific NPV), and Deltabaculovirus (dipteran-specific NPV) (Jehle et al., 2006). Baculoviruses are arthropod-specific viruses with rod-shaped nucleocapsids ranging in size from 30-60 nm x 250-300 nm. -
Evolution of the Insects
CY501-C11[407-467].qxd 3/2/05 12:56 PM Page 407 quark11 Quark11:Desktop Folder:CY501-Grimaldi:Quark_files: But, for the point of wisdom, I would choose to Know the mind that stirs Between the wings of Bees and building wasps. –George Eliot, The Spanish Gypsy 11HHymenoptera:ymenoptera: Ants, Bees, and Ants,Other Wasps Bees, and The order Hymenoptera comprises one of the four “hyperdi- various times between the Late Permian and Early Triassic. verse” insectO lineages;ther the others – Diptera, Lepidoptera, Wasps and, Thus, unlike some of the basal holometabolan orders, the of course, Coleoptera – are also holometabolous. Among Hymenoptera have a relatively recent origin, first appearing holometabolans, Hymenoptera is perhaps the most difficult in the Late Triassic. Since the Triassic, the Hymenoptera have to place in a phylogenetic framework, excepting the enig- truly come into their own, having radiated extensively in the matic twisted-wings, order Strepsiptera. Hymenoptera are Jurassic, again in the Cretaceous, and again (within certain morphologically isolated among orders of Holometabola, family-level lineages) during the Tertiary. The hymenopteran consisting of a complex mixture of primitive traits and bauplan, in both structure and function, has been tremen- numerous autapomorphies, leaving little evidence to which dously successful. group they are most closely related. Present evidence indi- While the beetles today boast the largest number of cates that the Holometabola can be organized into two major species among all orders, Hymenoptera may eventually rival lineages: the Coleoptera ϩ Neuropterida and the Panorpida. or even surpass the diversity of coleopterans (Kristensen, It is to the Panorpida that the Hymenoptera appear to be 1999a; Grissell, 1999). -
Wednesday, March 18, 2009
REPORT NO. ZONE Z-3-66 Not for Publication 5Z30 FEBRUARY 1966 BIOLOGICAL EVALUATION OF A RED-HEADED PINE SAWFLY INFESTATION ON THE OCALA NATIONAL FOREST, FLORlDA by L. E. Drake and W. H. Padgett INTRODUCTION A biological evaluation of a red-headed sawfly infestation on the Seminole Dist:r.ict of the Ocala National Forest, Florida, was made on January Z6 and 27, 1966, by L. E. Drake, Forest Insect and Disease Control Section with assistance from Bascom Perry, Forester, Seminole Ranger District. The infestation is scattered throughout 14,000 acres of uneven-aged longleaf pine with intermingled slash pine plantations. This is the first year of defoliation and there is no known history of past sawfly infestations on this area. However, a 3, 000-acre infestation of another sawfly species, Neodiprion excitans, occurred in adjoining Marion County in 1963. TECHNICAL INFORMATION Causal agent - The red-headed pine sawfly, Neodiprion lecontei (Fitch.). Host trees attacked - Longleaf pine, Pinus palustris Mill. was the primary host Ppecies. However, light de.foliation was observed on scattered slash pine, Pinus elliottii var. elliottii Engelm. Type of damage - The red-headed pine sawfly feeds on the needles of its host causing defoliation. This damage results in growth loss and repeated defoliation may cause mortality. Defoliation was observed on all age classes from reproduction to sawtimber. Complete defoliation wall noted only on sapling-sized trees lZ-15 years old. No mortality was observed• • Biological data - There are, at least, three generations of this insect each year in Florida and feeding apparently continues throughout the winter months.