Behavioral Ecology Symposium '94: Thomas 39 INVERTEBRATE PETS
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
New Aspects About Supella Longipalpa (Blattaria: Blattellidae)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Asian Pac J Trop Biomed 2016; 6(12): 1065–1075 1065 HOSTED BY Contents lists available at ScienceDirect Asian Pacific Journal of Tropical Biomedicine journal homepage: www.elsevier.com/locate/apjtb Review article http://dx.doi.org/10.1016/j.apjtb.2016.08.017 New aspects about Supella longipalpa (Blattaria: Blattellidae) Hassan Nasirian* Department of Medical Entomology and Vector Control, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran ARTICLE INFO ABSTRACT Article history: The brown-banded cockroach, Supella longipalpa (Blattaria: Blattellidae) (S. longipalpa), Received 16 Jun 2015 recently has infested the buildings and hospitals in wide areas of Iran, and this review was Received in revised form 3 Jul 2015, prepared to identify current knowledge and knowledge gaps about the brown-banded 2nd revised form 7 Jun, 3rd revised cockroach. Scientific reports and peer-reviewed papers concerning S. longipalpa and form 18 Jul 2016 relevant topics were collected and synthesized with the objective of learning more about Accepted 10 Aug 2016 health-related impacts and possible management of S. longipalpa in Iran. Like the Available online 15 Oct 2016 German cockroach, the brown-banded cockroach is a known vector for food-borne dis- eases and drug resistant bacteria, contaminated by infectious disease agents, involved in human intestinal parasites and is the intermediate host of Trichospirura leptostoma and Keywords: Moniliformis moniliformis. Because its habitat is widespread, distributed throughout Brown-banded cockroach different areas of homes and buildings, it is difficult to control. -
UNIVERSITY of CALIFORNIA RIVERSIDE Isolation
UNIVERSITY OF CALIFORNIA RIVERSIDE Isolation, Determination of Absolute Stereochemistry, and Asymmetric Synthesis of Insect Methyl-Branched Hydrocarbons A Dissertation submitted in the partial satisfaction of the requirements for the degree of Doctor of Philosophy in Chemistry by Jan Edgar Bello June 2014 Dissertation Committee: Dr. Jocelyn G. Millar, Chairperson Dr. Thomas H. Morton Dr. Catharine Larsen Copyright by Jan Edgar Bello 2014 The Dissertation of Jan Edgar Bello is approved: ________________________________________________________________ ________________________________________________________________ ________________________________________________________________ Committee Chairperson University of California, Riverside Acknowledgements This dissertation would not have been possible without the guidance, assistance, and support from both my academic and biological families. I would first and foremost like to thank my advisor Professor Jocelyn G. Millar, who has guided me through this rigorous process and has helped me become the chemical ecologist I am today. I would also like to thank my research group Dr. Steve McElfresh, Dr. Yunfan Zou, Dr. Rebeccah Waterworth, R. Max Collignon, Joshua Rodstein, Jackie Serrano, and Brian Hanley for all the suggestions, insect collecting, synthetic discussions, and experimental advise that have allowed me to complete this dissertation. I would like to send a huge thank you to my family who have always believed in me. To my mom and dad, thank you for your encouragement, for loving me, and for your support (both financial and emotional). To my siblings, Jonathan, Michelle, and John-C thank you for your encouragement and for praying for me, especially during the beginning of my PhD studies when things were overwhelming. I would also like to thank my friends, Ryan Neff, Lauren George, Jenifer N. -
A New Insect Trackway from the Upper Jurassic—Lower Cretaceous Eolian Sandstones of São Paulo State, Brazil: Implications for Reconstructing Desert Paleoecology
A new insect trackway from the Upper Jurassic—Lower Cretaceous eolian sandstones of São Paulo State, Brazil: implications for reconstructing desert paleoecology Bernardo de C.P. e M. Peixoto1,2, M. Gabriela Mángano3, Nicholas J. Minter4, Luciana Bueno dos Reis Fernandes1 and Marcelo Adorna Fernandes1,2 1 Laboratório de Paleoicnologia e Paleoecologia, Departamento de Ecologia e Biologia Evolutiva, Universidade Federal de São Carlos (UFSCar), São Carlos, São Paulo, Brazil 2 Programa de Pós Graduacão¸ em Ecologia e Recursos Naturais, Centro de Ciências Biológicas e da Saúde, Universidade Federal de São Carlos (UFSCar), São Carlos, São Paulo, Brazil 3 Department of Geological Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada 4 School of the Environment, Geography, and Geosciences, University of Portsmouth, Portsmouth, Hampshire, United Kingdom ABSTRACT The new ichnospecies Paleohelcura araraquarensis isp. nov. is described from the Upper Jurassic-Lower Cretaceous Botucatu Formation of Brazil. This formation records a gigantic eolian sand sea (erg), formed under an arid climate in the south-central part of Gondwana. This trackway is composed of two track rows, whose internal width is less than one-quarter of the external width, with alternating to staggered series, consisting of three elliptical tracks that can vary from slightly elongated to tapered or circular. The trackways were found in yellowish/reddish sandstone in a quarry in the Araraquara municipality, São Paulo State. Comparisons with neoichnological studies and morphological inferences indicate that the producer of Paleohelcura araraquarensis isp. nov. was most likely a pterygote insect, and so could have fulfilled one of the Submitted 6 November 2019 ecological roles that different species of this group are capable of performing in dune Accepted 10 March 2020 deserts. -
Social Context Modulates Idiosyncrasy of Behaviour in the Gregarious Cockroach Blaberus Discoidalis
bioRxiv preprint doi: https://doi.org/10.1101/028571; this version posted October 8, 2015. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Crall, Souffrant, Akandwanaho & Hescock, et al. 2015 – preprint version Social context modulates idiosyncrasy of behaviour in the gregarious cockroach Blaberus discoidalis James D. Crall1,2,*, André D. Souffrant1,*, Dominic Akandwanaho1,*, Sawyer D. Hescock1,*, Sarah E. Callan1,†, W. Melissa Coronado1,†, Maude W. Baldwin1, Benjamin L. de Bivort1,3,‡ 1 – Dept. of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA. 2 – Concord Field Station, Harvard University, Bedford, MA 01730, USA. 3 – Center for Brain Science, Harvard University, Cambridge, MA 02138, USA. * These authors contributed equally. † These authors contributed equally. ‡ Corresponding author: [email protected] Abstract Individuals are different, but they can work together to perform adaptive collective behaviours. Despite emerging evidence that individual variation strongly affects group performance, it is less clear to what extent individual variation is modulated by participation in collective behaviour. We examined light avoidance (negative phototaxis) in the gregarious cockroach Blaberus discoidalis, in both solitary and group contexts. Cockroaches in groups exhibit idiosyncratic light-avoidance performance that persists across days, with some individual cockroaches avoiding a light stimulus 75% of the time, and others avoiding the light just above chance (i.e. ~50% of the time). These individual differences are robust to group composition. Surprisingly, these differences do not persist when individuals are tested in isolation, but return when testing is once again done with groups. -
Assessing the Efficiency of Molecular Markers for the Species Identification of Gregarines Isolated from the Mealworm and Super Worm Midgut
Microorganisms 2018, 6, 119 1 of 20 Article Assessing the Efficiency of Molecular Markers for the Species Identification of Gregarines Isolated from the Mealworm and Super Worm Midgut Chiara Nocciolini 1, Claudio Cucini 2, Chiara Leo 2, Valeria Francardi 3, Elena Dreassi 4 and Antonio Carapelli 2,* 1 Polo d’Innovazione di Genomica Genetica e Biologia, 53100 Siena, Italy; [email protected] 2 Department of Life Sciences, University of Siena, 53100 Siena, Italy; [email protected] (C.C.); [email protected] (C.L.) 3 Consiglio per la ricerca in agricoltura e analisi dell’economia agraria – Centro di Difesa e Certificazione CREA-DC) Research Centre for Plant Protection and Certification, via di Lanciola 12/A, 50125 Firenze, Italy; [email protected] 4 Department of Biotechnology, Chemistry and Pharmacy, University of Siena, 53100 Siena, Italy; [email protected] * Correspondence: [email protected]; Tel.: +39-0577-234-410 Received: 28 September 2018; Accepted: 23 November 2018; Published: 27 November 2018 Abstract: Protozoa, of the taxon Gregarinasina, are a heterogeneous group of Apicomplexa that includes ~1600 species. They are parasites of a large variety of both marine and terrestrial invertebrates, mainly annelids, arthropods and mollusks. Unlike coccidians and heamosporidians, gregarines have not proven to have a negative effect on human welfare; thus, they have been poorly investigated. This study focuses on the molecular identification and phylogeny of the gregarine species found in the midgut of two insect species that are considered as an alternative source of animal proteins for the human diet: the mealworm Tenebrio molitor, and the super-worm Zophobas atratus (Coleoptera: Tenebrionidae). -
In the Cockroach, Blaberus Discoidalis
J Comp Physiol A (1998) 182: 23±33 Ó Springer-Verlag 1998 ORIGINAL PAPER J. T. Watson á R. E. Ritzmann Leg kinematics and muscle activity during treadmill running in the cockroach, Blaberus discoidalis : II. Fast running Accepted: 24 May 1997 Abstract We have combined kinematic and electromy- ogram (EMG) analysis of running Blaberus discoidalis to Introduction examine how middle and hind leg kinematics vary with Arthropod neuromuscular systems provide useful mod- running speed and how the fast depressor coxa (Df) and els in which to study problems involving control of lo- fast extensor tibia (FETi) motor neurons aect kine- comotion. The legs of various arthropods are matic parameters. In the range 2.5±10 Hz, B. discoidalis characterized by a pattern of few motor neurons sup- increases step frequency by altering the joint velocity plying each muscle, with each motor neuron having and by reducing the time required for the transition from markedly diverse properties. In all insects studied so far, ¯exion to extension. For both Df and FETi the timing of femoral depressor and tibial extensor muscles that are recruitment coincides with the maximal frequency seen used during stance are innervated by at most three axons for the respective slow motor neurons. Df is ®rst re- (Pearson and Iles 1971; Burrows and Hoyle 1972; Wil- cruited at the beginning of coxa-femur (CF) extension. son 1979). The triply innervated muscles receive a single FETi is recruited in the latter half of femur-tibia (FT) slow excitatory axon, a single fast excitatory axon, and a extension during stance. Single muscle potentials pro- common inhibitory axon shared with an undetermined duced by these fast motor neurons do not have pro- number of other muscles. -
Methane Production in Terrestrial Arthropods (Methanogens/Symbiouis/Anaerobic Protsts/Evolution/Atmospheric Methane) JOHANNES H
Proc. Nati. Acad. Sci. USA Vol. 91, pp. 5441-5445, June 1994 Microbiology Methane production in terrestrial arthropods (methanogens/symbiouis/anaerobic protsts/evolution/atmospheric methane) JOHANNES H. P. HACKSTEIN AND CLAUDIUS K. STUMM Department of Microbiology and Evolutionary Biology, Faculty of Science, Catholic University of Nijmegen, Toernooiveld, NL-6525 ED Nimegen, The Netherlands Communicated by Lynn Margulis, February 1, 1994 (receivedfor review June 22, 1993) ABSTRACT We have screened more than 110 represen- stoppers. For 2-12 hr the arthropods (0.5-50 g fresh weight, tatives of the different taxa of terrsrial arthropods for depending on size and availability of specimens) were incu- methane production in order to obtain additional information bated at room temperature (210C). The detection limit for about the origins of biogenic methane. Methanogenic bacteria methane was in the nmol range, guaranteeing that any occur in the hindguts of nearly all tropical representatives significant methane emission could be detected by gas chro- of millipedes (Diplopoda), cockroaches (Blattaria), termites matography ofgas samples taken at the end ofthe incubation (Isoptera), and scarab beetles (Scarabaeidae), while such meth- period. Under these conditions, all methane-emitting species anogens are absent from 66 other arthropod species investi- produced >100 nmol of methane during the incubation pe- gated. Three types of symbiosis were found: in the first type, riod. All nonproducers failed to produce methane concen- the arthropod's hindgut is colonized by free methanogenic trations higher than the background level (maximum, 10-20 bacteria; in the second type, methanogens are closely associated nmol), even if the incubation time was prolonged and higher with chitinous structures formed by the host's hindgut; the numbers of arthropods were incubated. -
94: Frank & Mccoy Intro. 1 INTRODUCTION to INSECT
Behavioral Ecology Symposium ’94: Frank & McCoy Intro. 1 INTRODUCTION TO INSECT BEHAVIORAL ECOLOGY : THE GOOD, THE BAD, AND THE BEAUTIFUL: NON-INDIGENOUS SPECIES IN FLORIDA INVASIVE ADVENTIVE INSECTS AND OTHER ORGANISMS IN FLORIDA. J. H. FRANK1 AND E. D. MCCOY2 1Entomology & Nematology Department, University of Florida, Gainesville, FL 32611-0620 2Biology Department and Center for Urban Ecology, University of South Florida, Tampa, FL 33620-5150 ABSTRACT An excessive proportion of adventive (= “non-indigenous”) species in a community has been called “biological pollution.” Proportions of adventive species of fishes, am- phibia, reptiles, birds and mammals in southern Florida range from 16% to more than 42%. In Florida as a whole, the proportion of adventive plants is about 26%, but of in- sects is only about 8%. Almost all of the vertebrates were introduced as captive pets, but escaped or were released into the wild, and established breeding populations; few arrived as immigrants (= “of their own volition”). Almost all of the plants also were in- troduced, a few arrived as immigrants (as contaminants of shipments of seeds or other cargoes). In contrast, only 42 insect species (0.3%) were introduced (all for bio- logical control of pests, including weeds). The remainder (about 946 species, or 7.6%) arrived as undocumented immigrants, some of them as fly-ins, but many as contami- nants of cargoes. Most of the major insect pests of agriculture, horticulture, human- made structures, and the environment, arrived as hitchhikers (contaminants of, and stowaways in, cargoes, especially cargoes of plants). No adventive insect species caus- ing problems in Florida was introduced (deliberately) as far as is known. -
Arima Valley Bioblitz 2013 Final Report.Pdf
Final Report Contents Report Credits ........................................................................................................ ii Executive Summary ................................................................................................ 1 Introduction ........................................................................................................... 2 Methods Plants......................................................................................................... 3 Birds .......................................................................................................... 3 Mammals .................................................................................................. 4 Reptiles and Amphibians .......................................................................... 4 Freshwater ................................................................................................ 4 Terrestrial Invertebrates ........................................................................... 5 Fungi .......................................................................................................... 6 Public Participation ................................................................................... 7 Results and Discussion Plants......................................................................................................... 7 Birds .......................................................................................................... 7 Mammals ................................................................................................. -
MADAGASCAR HISSING COCKROACH Class Order Family Genus Species Insecta Blattaria Blaberidae Gromphadorhina Portentosa
MADAGASCAR HISSING COCKROACH Class Order Family Genus Species Insecta Blattaria Blaberidae Gromphadorhina portentosa Range: Madagascar Habitat: Decaying leaf litter, rotting wood on forest floors. Niche: Nocturnal, omnivorous, terrestrial Diet: Wild: Scavengers, decaying plant and animal material Zoo: Finely ground chick or hog meal, vegetables, fruit Special Adaptations: Large, wingless species. Males and females are the same size at maturity, averaging three to four inches. Males are easily distinguished from females by the presence of two horns on their prothorax. Females lack these horns. Further methods of distinguishing the males from females include looking at the thorax, the antennae, and at the tip of the abdomen. In the male, the prothorax stands out in two protuberances, making the prothorax appear to be the head of a vertebrate animal. Antennae in females lack hair, and the abdomen in males has a narrower ventral plate than that of the female. This species communicates by a loud hissing sound made by air forced through spiracles on the sides of their bodies. Females are ovoviparous; they bear live young. The female retains the ootheca (egg case) inside her body, and after birth, the young will feed on the empty egg packet, which is passed after they are born. At warm temperatures, the young will reach adult size in 2-3 months. Other: They lack the odor usually associated with cockroaches or their feces. They do not bite and will usually hide when disturbed. TROPICAL WOOD COCKROACH Class Order Family Genus Species Insecta Blattaria Blattidae Blaberus spp Range: Central and South America Habitat: Tropical & subtropical forests, humidity above 60% Niche: Nocturnal, omnivorous, scavengers, terrestrial Diet: Wild: decaying plant and animal material Blaberus giganteus Zoo: Special Adaptations: Cockroaches leave chemical trails in their feces as well as emitting airborne pheromones for swarming and mating. -
False Death's Head Cockroaches Latin Name:Blaberus Discoidalis
Husbandry Data Sheet Common Name: False Death's Head Cockroaches Latin Name:Blaberus discoidalis Family:Blaberidae Order:Dictyoptera Class:Insecta Phylum:Arthropoda Natural History:The False Death's Head Cockroach (Blaberus discoidalis) is found throughout the northern part of South America. In the wild this species can be found in caves, holes in trees and under bark. During mating behaviour the males ‘pump’ their wings, raising them up and down to attract the attention of the female. This cockroach, like many others, produces a distinctive smell when attacked. Permits Required:Yes Life Stage:All Ease of Care:Easy Housing: Temp:75-85 degrees F Humidity:60%-80% Substrate:50:50 mixture of sand and compost. # of Animals per Exhibit:200 Choose One:Colony Compatible Species:N/A Enclosure Description: 10 gallon aquarium. Lighting/Photoperiod: Flourescent lighting on a 12 hour period. Furniture/Props:4" plastic coated hardware cloth climbing structure and plastic tubes. Escape Concerns:Although this species is not noted as being a climber, a screen cover is securely fastened to the tank. Other Concerns/Precautions: Husbandry Diet/Frequency of Feeding:Mixed vegetables and Mazuri primate biscuits Water Source/FrequencyMoisture from food as well as a 4" petri dish with rocks. Care: Daily Enrichment:Cork bark to hide under and wire tubes for climbing structres. Medical/Health Concerns:If the soil becomes too moist mites can become a challenge. Treatment:Substrate change or drying out the sunstrate help keep the mites under control. Keeper Safety: N/A Other Concerns/Precautions:All old food and substrate is placed in a freezer for one week prior to being discarded to destroy any nymphs missed in cleaning. -
(Bacillus Cereus) Symbionts in the Cockroach Blaberus Giganteus: Dietary Influences on Bacterial Development and Population Density
R L\Bfl ' Symbiosis, 27 (1999) 109-123 109 Balaban, Philadelphia/Rehovot Arthromitus (Bacillus cereus) Symbionts in the Cockroach Blaberus giganteus: Dietary Influences on Bacterial Development and Population Density LAWRENCE FEINBERGl, JEREMY JORGENSEN2, AARON HASELTON3, ALISON PITT4, RIVKA RUDNER5, and LYNN MARGULIS6* l Deparimeni of Biology, 2Department of Organismic and Evolutionary Biology, 3Department of Entomology, and +Department of Wildlife, University of Massachusetts, Amherst, MA 01003, 5Department of Biology, Hunter College, New York, NY 10021, and 6Department of Geosciences, University of Massachusetts, Amherst, MA 01003-5820, USA, Tel. +413-545-3244, Fax. +413-545-1200 Received June 17, 1999;Accept ed August 15, 1999 Abstract The filamentous spore-forming bacterium Arthromitus, discovered in termites, millipedes, sow bugs and other soil-dwelling arthropods by Leidy (1850), is the intestinal stage of Bacillus cereus. We extend the range of Arthromitus habitats to include the hindgut of Blaberus giganteus, the large tropical American cockroach. The occurrence and morphology of the intestinal form of the bacillus were compared in individual cockroaches (n=24) placed on four different diet regimes: diurnally maintained insects fed (1) dog food, (2) soy protein only, (3) purified cellulose only, and (4) a dog food-fed group maintained in continuous darkness. Food quality exerted strong influence on population densities and developmental stages of the filamentous bacterium and on fecal pellet composition. The most dramatic rise in Arthromitus populations, defined as the spore-forming filament intestinal stage, occurred in adult cockroaches kept in the dark on a dog food diet. Limited intake of cellulose or protein alone reduced both the frequency of Arthromitus filaments and the rate of weight gain of the insects.