Jack Jumper Ant Allergy – a Uniquely Australian Problem
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The Mesosomal Anatomy of Myrmecia Nigrocincta Workers and Evolutionary Transformations in Formicidae (Hymeno- Ptera)
7719 (1): – 1 2019 © Senckenberg Gesellschaft für Naturforschung, 2019. The mesosomal anatomy of Myrmecia nigrocincta workers and evolutionary transformations in Formicidae (Hymeno- ptera) Si-Pei Liu, Adrian Richter, Alexander Stoessel & Rolf Georg Beutel* Institut für Zoologie und Evolutionsforschung, Friedrich-Schiller-Universität Jena, 07743 Jena, Germany; Si-Pei Liu [[email protected]]; Adrian Richter [[email protected]]; Alexander Stößel [[email protected]]; Rolf Georg Beutel [[email protected]] — * Corresponding author Accepted on December 07, 2018. Published online at www.senckenberg.de/arthropod-systematics on May 17, 2019. Published in print on June 03, 2019. Editors in charge: Andy Sombke & Klaus-Dieter Klass. Abstract. The mesosomal skeletomuscular system of workers of Myrmecia nigrocincta was examined. A broad spectrum of methods was used, including micro-computed tomography combined with computer-based 3D reconstruction. An optimized combination of advanced techniques not only accelerates the acquisition of high quality anatomical data, but also facilitates a very detailed documentation and vi- sualization. This includes fne surface details, complex confgurations of sclerites, and also internal soft parts, for instance muscles with their precise insertion sites. Myrmeciinae have arguably retained a number of plesiomorphic mesosomal features, even though recent mo- lecular phylogenies do not place them close to the root of ants. Our mapping analyses based on previous morphological studies and recent phylogenies revealed few mesosomal apomorphies linking formicid subgroups. Only fve apomorphies were retrieved for the family, and interestingly three of them are missing in Myrmeciinae. Nevertheless, it is apparent that profound mesosomal transformations took place in the early evolution of ants, especially in the fightless workers. -
Hymenoptera: Formicidae) Along an Elevational Gradient at Eungella in the Clarke Range, Central Queensland Coast, Australia
RAINFOREST ANTS (HYMENOPTERA: FORMICIDAE) ALONG AN ELEVATIONAL GRADIENT AT EUNGELLA IN THE CLARKE RANGE, CENTRAL QUEENSLAND COAST, AUSTRALIA BURWELL, C. J.1,2 & NAKAMURA, A.1,3 Here we provide a faunistic overview of the rainforest ant fauna of the Eungella region, located in the southern part of the Clarke Range in the Central Queensland Coast, Australia, based on systematic surveys spanning an elevational gradient from 200 to 1200 m asl. Ants were collected from a total of 34 sites located within bands of elevation of approximately 200, 400, 600, 800, 1000 and 1200 m asl. Surveys were conducted in March 2013 (20 sites), November 2013 and March–April 2014 (24 sites each), and ants were sampled using five methods: pitfall traps, leaf litter extracts, Malaise traps, spray- ing tree trunks with pyrethroid insecticide, and timed bouts of hand collecting during the day. In total we recorded 142 ant species (described species and morphospecies) from our systematic sampling and observed an additional species, the green tree ant Oecophylla smaragdina, at the lowest eleva- tions but not on our survey sites. With the caveat of less sampling intensity at the lowest and highest elevations, species richness peaked at 600 m asl (89 species), declined monotonically with increasing and decreasing elevation, and was lowest at 1200 m asl (33 spp.). Ant species composition progres- sively changed with increasing elevation, but there appeared to be two gradients of change, one from 200–600 m asl and another from 800 to 1200 m asl. Differences between the lowland and upland faunas may be driven in part by a greater representation of tropical and arboreal-nesting sp ecies in the lowlands and a greater representation of subtropical species in the highlands. -
The Cypress Pine Sawfly Subspecies Zenarge Turneri Turneri Rohwer and Zenarge Turneri Rabus Moore
This document has been scanned from hard-copy archives for research and study purposes. Please note not all information may be current. We have tried, in preparing this copy, to make the content accessible to the widest possible audience but in some cases we recognise that the automatic text recognition maybe inadequate and we apologise in advance for any inconvenience this may cause. FORESTRY COMMISSION OF N.S.W. DIVISION OF FOREST MANAGEMENT RESEARCH NOTE No. 13 Published March, 1963 THE CYPRESS PINE SAWFLY SUBSPECIES ZENARGE TURNER! TURNER! ROHWER and ZENARGE TURNERI RABUS MOORE AUTHOR K.M.MOORE G 16325 FORESTRY COMMISSION OF x.s.w, DIVISION OF FOREST MANAGEMENT RESEARCH NOTE No. 13 Published March, 1963 THE CYPRESS PINE SAWFLY SUBSPECIES ZENARGE TURNERI TURNERI ROHWER AND ZENARGE TURNERI RABUS MOORE AUTHOR K. M. MOORE G 16325-1 The Cypress Pine Sawfly Subspecies Zenarge turneri turneri Rohwer and Zenarge turneri rabus Moore K. M. MooRE SYNOPSIS During investigations into the taxonomy and biology of the cypress pine sawfly, previously known as Zenarge turneri, and which had caused extensive damage to stands of Callitris hugelii (Carr.) Franco on several State Forests in western New South Wales, on experimental plots of that host in highland and coastal districts and on ornamental Cupressus and Callitris spp., the sawflyspecieswas found to consist of two subspecies. The morphology, biology, distribution and hosts by which the sub species may be determined, are given, and the revised taxonomic position has been presented previously (Moore 1962)a. INTRODUCTION Numerous species of sawflies occur in New South Wales, but Zenarge turned turneri Rohwer and Zenarge turneri rabus Moore are the only sawflies recorded as attacking Callttris and Cupressus spp., and they are host-specificto these two genera. -
'Jack Jumper' Ant Venom by Mass Spectrometry
Characterisation of Major Peptides in ‘Jack Jumper’ Ant Venom by Mass Spectrometry Noel W. Davies 1* , Michael D.Wiese 2 and Simon G. A. Brown 3 1. Central Science Laboratory University of Tasmania Private Bag 74 Hobart 7001 Tasmania, AUSTRALIA Fax: 61 3 6226 2494 Email: [email protected] 2. Department of Pharmacy Royal Hobart Hospital GPO Box 1061L Hobart, Tasmania 7001 Australia 3 Department of Emergency Medicine Royal Hobart Hospital GPO Box 1061L Hobart, Tasmania 7001 Australia * Corresponding author : Running title: ‘Jack Jumper’ ant venom peptides 1 Abstract: The jack jumper ant, Myrmecia pilosula , is endemic to South-Eastern Australia, where around 2.7% of the population has a history of systemic allergic reactions (anaphylaxis) to its venom. Previous work had indicated that there were several allergenic peptides derived from the cDNA Myr p 1, the major expressed allergenic product being a 56-residue peptide (Myr p 1 57 →112, "pilosulin 1", ~6052 Da). Another major allergen had been described as a 27 residue peptide derived from the cDNA Myr p 2 (Myr p 2 49 →75, "pilosulin 2", ~3212 Da), possibly existing as part of a disulfide complex. As a preliminary step in detailed stability studies of a pharmaceutical product used for venom immunotherapy, LC-MS and Edman sequencing analysis of venom collected from various locations by both electrical stimulation and venom sac dissection was undertaken. More than 50 peptides in the 4kDa to 9kDa range were detected in LC-MS analyses. A subsequence of Myr p 2 was found as part of the major peptide present in all samples; this was a bis- disulphide linked, antiparallel aligned heterodimer consisting of Myr p 2 49 →74, (des-Gly 27 -pilosulin 2, ~3155 Da) and a previously unreported peptide of ~2457 Da. -
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RESEARCH Causes of ant sting anaphylaxis in Australia: the Australian Ant Venom Allergy Study Simon G A Brown, Pauline van Eeden, Michael D Wiese, Raymond J Mullins, Graham O Solley, Robert Puy, Robert W Taylor and Robert J Heddle he prevalence of systemic allergy to ABSTRACT native ant stings in Australia is as high as 3% in areas where these Objective: To determine the Australian native ant species associated with ant sting T anaphylaxis, geographical distribution of allergic reactions, and feasibility of diagnostic insects are commonly encountered, such as Tasmania and regional Victoria.1,2 In one venom-specific IgE (sIgE) testing. large Tasmanian emergency department Design, setting and participants: Descriptive clinical, entomological and study, ant sting allergy was the most com- immunological study of Australians with a history of ant sting anaphylaxis, recruited in mon cause of anaphylaxis (30%), exceeding 2006–2007 through media exposure and referrals from allergy practices and emergency cases attributed to bees, wasps, antibiotics physicians nationwide. We interviewed participants, collected entomological or food.3 specimens, prepared reference venom extracts, and conducted serum sIgE testing Myrmecia pilosula (jack jumper ant [JJA]) against ant venom panels relevant to the species found in each geographical region. is theThe major Medical cause Journal of ant ofsting Australia anaphylaxis ISSN: Main outcome measures: Reaction causation attributed using a combination of ant 2 in Tasmania.0025-729X A 18double-blind, July 2011 195 randomised 2 69-73 identification and sIgE testing. placebo-controlled©The Medical Journaltrial has of Australiademonstrated 2011 Results: 376 participants reported 735 systemic reactions. Of 299 participants for whom the effectivenesswww.mja.com.au of JJA venom immuno- a cause was determined, 265 (89%; 95% CI, 84%–92%) had reacted clinically to Myrmecia therapyResearch (VIT) to reduce the risk of sting species and 34 (11%; 95% CI, 8%–16%) to green-head ant (Rhytidoponera metallica). -
Differential Investment in Brain Regions for a Diurnal and Nocturnal Lifestyle in Australian Myrmecia Ants
Received: 12 July 2018 Revised: 7 December 2018 Accepted: 22 December 2018 DOI: 10.1002/cne.24617 RESEARCH ARTICLE Differential investment in brain regions for a diurnal and nocturnal lifestyle in Australian Myrmecia ants Zachary B. V. Sheehan1 | J. Frances Kamhi1 | Marc A. Seid1,2 | Ajay Narendra1 1Department of Biological Sciences, Macquarie University, Sydney, New South Wales, Abstract Australia Animals are active at different times of the day. Each temporal niche offers a unique light envi- 2Biology Department, Neuroscience Program, ronment, which affects the quality of the available visual information. To access reliable visual The University of Scranton, Scranton, signals in dim-light environments, insects have evolved several visual adaptations to enhance Pennsylvania their optical sensitivity. The extent to which these adaptations reflect on the sensory processing Correspondence Department of Biological Sciences, Macquarie and integration capabilities within the brain of a nocturnal insect is unknown. To address this, University, 205 Culloden Road, Sydney, NSW we analyzed brain organization in congeneric species of the Australian bull ant, Myrmecia, that 2109, Australia. rely predominantly on visual information and range from being strictly diurnal to strictly noctur- Email: [email protected] nal. Weighing brains and optic lobes of seven Myrmecia species, showed that after controlling Funding information for body mass, the brain mass was not significantly different between diurnal and nocturnal Australian Research Council, Grant/Award Numbers: DP150101172, FT140100221 ants. However, the optic lobe mass, after controlling for central brain mass, differed between day- and night-active ants. Detailed volumetric analyses showed that the nocturnal ants invested relatively less in the primary visual processing regions but relatively more in both the primary olfactory processing regions and in the integration centers of visual and olfactory sen- sory information. -
Jack Jumper Ants – August 2010 Biosecurity Fact Sheet Current As at October 2010
DPIPWE fact sheet – Jack jumper ants – August 2010 Biosecurity fact sheet Current as at October 2010 Jack Jumper Ants Myrmecia pilosula complex of species (also known as jumper ants or hopper ants) Australia, including Tasmania. They also occur in open habitats, including pastures, gardens and lawns that have not been much cultivated and are near light bush, such as around new housing. They prefer fine gravel and sandy soil. They like to forage for food near eucalypts, wattles and the native understorey bushes associated with those trees. They collect small insects, honeydew from sap-sucking bugs and nectar to take back to their nest where it is fed to ant grubs. photograph © Alex Wild 2005 Jack jumper nests contain hundreds or photograph © Alex Wild 2005 thousands of ants, but this is considerably less than many smaller pest ants. In the nest the Jack jumpers (also known as jumper ants, queen, who lays all the eggs, can survive a hopper ants, jumping jacks) are medium sized decade. The worker ants can live a couple of ants, 8-10mm long with a black body but pale years. The entrance to the nest is often jaws and legs. They can jump 10cm repeatedly surrounded by a pile of sand and pebbles 6cm in when defending themselves. They are related diameter with a central hole 1cm diameter. to the larger, less aggressive and less active inchman ants which are 3cm long. The only effective way of controlling jumper ants is to treat their nests with a dust or sandy There are many species of both jack jumpers formulation of one of the registered and inchman ants in Australia . -
Evidence for UV-Green Dichromacy in the Basal Hymenopteran Sirex Noctilio
www.nature.com/scientificreports OPEN Evidence for UV‑green dichromacy in the basal hymenopteran Sirex noctilio (Siricidae) Quentin Guignard 1*, Johannes Spaethe 2, Bernard Slippers 3, Martin Strube‑Bloss 2,5 & Jeremy D. Allison 1,4 A precondition for colour vision is the presence of at least two spectral types of photoreceptors in the eye. The order Hymenoptera is traditionally divided into the Apocrita (ants, bees, wasps) and the Symphyta (sawfies, woodwasps, horntails). Most apocritan species possess three diferent photoreceptor types. In contrast, physiological studies in the Symphyta have reported one to four photoreceptor types. To better understand the evolution of photoreceptor diversity in the Hymenoptera, we studied the Symphyta Sirex noctilio, which belongs to the superfamily Siricoidea, a closely related group of the Apocrita suborder. Our aim was to (i) identify the photoreceptor types of the compound eye by electroretinography (ERG), (ii) characterise the visual opsin genes of S. noctilio by genomic comparisons and phylogenetic analyses and (iii) analyse opsin mRNA expression. ERG measurements revealed two photoreceptor types in the compound eye, maximally sensitive to 527 and 364 nm. In addition, we identifed three opsins in the genome, homologous to the hymenopteran green or long‑wavelength sensitive (LW) LW1, LW2 and ultra‑violet sensitive (UV) opsin genes. The LW1 and UV opsins were found to be expressed in the compound eyes, and LW2 and UV opsins in the ocelli. The lack of a blue or short‑wavelength sensitive (SW) homologous opsin gene and a corresponding receptor suggests that S. noctilio is a UV‑green dichromate. Te ability to see colours, i.e. -
The Insect Sting Pain Scale: How the Pain and Lethality of Ant, Wasp, and Bee Venoms Can Guide the Way for Human Benefit
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 27 May 2019 1 (Article): Special Issue: "Arthropod Venom Components and their Potential Usage" 2 The Insect Sting Pain Scale: How the Pain and Lethality of Ant, 3 Wasp, and Bee Venoms Can Guide the Way for Human Benefit 4 Justin O. Schmidt 5 Southwestern Biological Institute, 1961 W. Brichta Dr., Tucson, AZ 85745, USA 6 Correspondence: [email protected]; Tel.: 1-520-884-9345 7 Received: date; Accepted: date; Published: date 8 9 Abstract: Pain is a natural bioassay for detecting and quantifying biological activities of venoms. The 10 painfulness of stings delivered by ants, wasps, and bees can be easily measured in the field or lab using the 11 stinging insect pain scale that rates the pain intensity from 1 to 4, with 1 being minor pain, and 4 being extreme, 12 debilitating, excruciating pain. The painfulness of stings of 96 species of stinging insects and the lethalities of 13 the venoms of 90 species was determined and utilized for pinpointing future promising directions for 14 investigating venoms having pharmaceutically active principles that could benefit humanity. The findings 15 suggest several under- or unexplored insect venoms worthy of future investigations, including: those that have 16 exceedingly painful venoms, yet with extremely low lethality – tarantula hawk wasps (Pepsis) and velvet ants 17 (Mutillidae); those that have extremely lethal venoms, yet induce very little pain – the ants, Daceton and 18 Tetraponera; and those that have venomous stings and are both painful and lethal – the ants Pogonomyrmex, 19 Paraponera, Myrmecia, Neoponera, and the social wasps Synoeca, Agelaia, and Brachygastra. -
Common Names for Australian Ants (Hymenoptera: Formicidae)
Australian Journal of Entomology (2002) 41, 285–293 Common names for Australian ants (Hymenoptera: Formicidae) Alan N Andersen CSIRO Sustainable Ecosystems, Tropical Ecosystems Research Centre, PMB 44, Winnellie, NT 0822, Australia. Abstract Most insects do not have common names, and this is a significant barrier to public interest in them, and to their study by non-specialists. This holds for even highly familiar insect groups such as ants. Here, I propose common names for all major native Australian ant genera and species-groups, as well as for many of the most abundant and distinctive species. Sixty-two genera, 142 species-groups and 50 species are given names. The naming system closely follows taxonomic structure; typically a genus is given a general common name, under which species-group and species names are nested. Key words ant species, communicating entomology, species-groups, taxonomic nomenclature. INTRODUCTION ‘little black ones’ (the remaining several thousand Australian species). Here, I attempt to redress this situation by propos- Common names are powerful aids for the popular communi- ing common names for all major native Australian ant genera cation of information about plant and animal species. Such and species-groups, as well as for many abundant and names use familiar and easily remembered words, in contrast distinctive species. to the taxonomic nomenclature that is so daunting for most people without formal scientific training. All higher-profile vertebrates and vascular plants have widely accepted common names. These increase the accessibility of these species to a PROPOSED ANT COMMON NAMES wide public audience, and promote interest in them. In Proposed common names, and explanations for them, for contrast, the vast majority of insects and other arthropods 62 genera, 142 species-groups and 50 species of Australian have no common name beyond the ordinal level, unless they ants are presented in Appendix I, Table A1. -
The Sting Bulb Gland in Myrmecia and Nothomyrmecia (Hymenoptera" Formicidae): a New Exocrine Gland in Ants
Int. J. lpt~ectMorphol. & Emb~vol., Vol. 19, No. 2, pp. 133-139, 1990 0020-7322/90 $3.00+ .IR) Printed in Great Britain © 1990 Pergamon Press plc THE STING BULB GLAND IN MYRMECIA AND NOTHOMYRMECIA (HYMENOPTERA" FORMICIDAE): A NEW EXOCRINE GLAND IN ANTS JOHAN BILLEN Zoological Institute, University of Leuven, Naamsestraat 59, B-3000 Leuven, Belgium (Accepted 7 December 1989) Abstract--A new exocrine gland has been discovered within the sting of the endemic Australian ants of the genera Myrmecia and Nothomyrmecia (Hymenoptera : Formicidae). It consists of approximately 20 secretory cells with their accompanying duct cells, located between the ducts of the venom and Dufour glands in the proximal part of ths sting bulb, hence my suggestion to designate it as the sting bulb gland. Ultrastructural examination reveals the development of both granular and smooth endoplasmic reticulum in the glandular cells, which possibly may indicate the elaboration of a rather complex secretion. Although the function of the gland remains unknown, its exclusive presence in these ants provides another argument for a closer phylogenetic relationship between both genera than is reflected by their actual classification. Index descriptors (in addition to those in title): Myrmecia, Nothomyrmecia, morphology, ultrastructure, phylogeny. INTRODUCTION THE STING in social insects has evolved, from its original function as an ovipositor, towards an effective weapon for colony defense. The usually very sharp posterior end of the heavily sclerotized sting shaft and lancets provide the mechanical equipment for piercing the prey or enemy, while exocrine glands produce the venom compounds to be injected in the victim. The glandular apparatus of the sting comprises the venom gland and Dufour's gland, which are the modified accessory glands of the female reproductive system, and both of which open through the anterior side of the sting base in the Formicidae (Billen, 1987a). -
The Coexistence
Myrmecological News 18 25-32 Vienna, March 2013 Mating system and population genetic structure of the bulldog ant Myrmecia pavida (Hymenoptera: Formicidae) Paula CHAPPELL, Katherine ROBERTS, Boris BAER & William O.H. HUGHES Abstract Understanding the evolution of the alternative mating strategies of monandry and polyandry is a fundamental problem in evolutionary biology because of the cost-benefit trade-offs associated with mating for females. The problem is parti- cularly intriguing in the social insects because queens in most species appear to be obligately monandrous (i.e., only a single male fathers their offspring), while those in a minority of species have evolved high, and sometimes extreme, poly- andry. One group which may shed particular insight is the ant subfamily Myrmeciinae (Myrmecia and Nothomyrmecia). Here we examine the population and colony genetic structure of the bulldog ant Myrmecia pavida CLARK, 1951 by geno- typing offspring workers from 45 colonies. We find little evidence of geographic structuring or inbreeding in the popu- lation, indicating that the species outbreeds, most probably in mating swarms. We also find that queens of M. pavida show moderately high polyandry, with 84% having mated with between two and seven males, and an overall mean ob- served mating frequency of 3.8. This is significantly higher than previously reported for queens of Nothomyrmecia macrops, in which most females mate singly. This was similar to that of M. pyriformis, M. brevinoda, and M. pilosula, the three congenerics for which mating frequencies have recently been reported. The two genera in the Myrmeciinae therefore appear to show multiple transitions in mating frequency and further investigation of the subfamily may be highly infor- mative for disentangling the forces driving the evolution of alternative mating strategies.