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Ants of the Genus Lordomyrma Emery (2) the Japanese L. Azumai
Zootaxa 3282: 45–60 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) Ants of the genus Lordomyrma Emery (2) The Japanese L. azumai (Santschi) and six new species from India, Viet Nam and the Philippines (Hymenoptera: Formicidae: Myrmicinae) ROBERT W. TAYLOR Research School of Biological Sciences, Australian National University, Canberra, ACT, 2600, Australia. Honorary Research Fellow, CSIRO Ecosystem Sciences, Canberra, ACT, 2601, Australia. E-mail: [email protected] Abstract Lordomyrma is recorded for the first time from India and mainland southeast Asia. The Japanese L. azumai is reviewed and six new worker-based species described: L. lakshmi (Kerala State, India); L. hmong (Lao Cai Province, Vietnam); L. diwata, L. emarginata and L. idianale (Mt Isarog, Luzon, Philippines) and L. limatula (Leyte, Philippines). Gynes are characterized for L. azumai, L. hmong and L. limatula. All taxa are diagnosed, illustrated, and their affinities discussed. Key words: Ants, Formicidae, Lordomyrma, Stenamma, Lasiomyrma, taxonomy, new species, biogeography, Japan, Hon- shu, Shikoku, Kyushu, India, Kerala, Viet Nam, Lao Cai, Philippines, Luzon, Leyte, Mt Isarog Introduction This is the second paper (following Taylor, 2009) of a project seeking to review and name the many known undescribed morphospecies reasonably considered taxonomically congeneric with the somewhat aberrant ant Lordomyrma furcifera Emery (type-species of Lordomyrma Emery 1897) and its more conservative putative relative L. azumai (Santschi). The latter is arguably the least morphologically derived known Lordomyrma species (Taylor, 2009) and its characteristics may thus be very generally considered archetypal for the genus. In this analysis L. -
Lordomyrma (Hymenoptera: Formicidae) of the Fiji Islands1
Fiji Arthropods VI. Edited by Neal L. Evenhuis & Daniel J. Bickel. Bishop Museum Occasional Papers 90: 9–42 (2006). Lordomyrma (Hymenoptera: Formicidae) of the Fiji Islands1 ELI M. SARNAT Department of Entomology, University of California, Davis, One Shields Ave, Davis, California 95616, USA; email: [email protected] Abstract: This revision treats the members of the ant genus Lordomyrma (Formicidae: Myrmicinae) occurring in Fiji. Ten species are recognized, of which four are new: L. cur- vata sp. n., L. desupra sp. n., L. levifrons (Mann) stat. n., L. polita (Mann) stat. n., L. rugosa (Mann), L. sukuna sp. n., L. stoneri (Mann) stat. n., L. striatella (Mann), L. tor- tuosa (Mann), and L. vuda sp. n. Descriptions of each species are provided, along with distribution maps and a key for the identification of workers. Additional figures and iden- tification tools are available on Antweb <http://www.antweb.org/fiji.jsp>. A preliminary comparison with Lordomyrma from Australia, New Guinea, and New Caledonia is fol- lowed by a discussion of the distribution of species within Fiji and an outline of future research directions pertaining to the taxonomy, biogeography and conservation of the Fijian species. BACKGROUND The genus Lordomyrma (Formicidae: Myrmicinae) Emery is comprised of relatively uncommon and often elegantly sculptured ants occurring in the Australian and Oriental regions. Species have been described from Japan, New Guinea, eastern Australia, New Caledonia, the Solomon Islands and Fiji (Bolton 1995), with additional undescribed species being reported from Borneo (Brühl et al. 1998). Of the 24 currently recognized species in the genus (including those described here), ten are endemic to the Fijian arch- ipelago. -
Timeline of Genomics
Timeline of Genomics Timeline of Genomics (1865-1900)* Year Event and Theoretical Implication/Extension Reference 1865 Gregor Mendel establishes the laws of segregation and Mendel, G. 1865. Versuche Äuber independent assortment. Pflanzenhybriden. Verh. Naturforsch. Ver. BrÄunn 4: 3-47. 1866 Ernst Heinrich HÄackel hypotheses that the nucleus HÄackel, E. 1866. Generelle Morphologie of a cell transmits its hereditary information. der Organismen. G. Reimer, Berlin, Ger- many. 1867 Wilhelm Friedrich Benedict Hofmeister estab- Hofmeister, W. 1867. Die Lehre von der lishes the regularity of the \dissolution" of the nucleus Pfanzenzelle. Verlag von Wilhelm Engel- prior to division of the maternal cell, and the appear- mann, Leipzig, Germany. ance of new nuclei in daughter cells. 1869 Francis Galton claims that intelligence is inherited as Galton, F. 1869. Hereditary Genius: a straightforward trait. An Inquiry into Its Laws and Conse- quences. The Macmillan Co., London, United Kingdom. 1871 Johann Friedrich Miescher discovers and isolates Miescher, F. 1871. UberÄ die chemis- NUCLEIN (DNA) in the cells from pus in open che Zusammensetzung der Eiterzellen. wounds. It became known as nucleic acid after 1874, In Medicinisch-chemische Untersuchun- when Miescher separated it into a protein and an acid gen aus dem Laboratorium fÄur ange- molecule. wandte Chemie zu TÄubingen. (Hoppe- Seyler, F., ed.) 4: 441-460. A. Hirschwald, Berlin, Germany. Charles Darwin describes the role of sexual selection Darwin, C. 1871. The Descent of Man in evolution for the ¯rst time. and Selection in Relation to Sex. John Murray, London, United Kingdom. 1873 Friedrich Anton Schneider ¯rst describes pictures of Schneider, A. 1873. Untersuchungen the nucleus in division (mitosis) in cells of cleaving eggs Äuber Plathelminthen. -
Zootaxa, Ants of the Genus Lordomyrma Emery
Zootaxa 1979: 16–28 (2009) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2009 · Magnolia Press ISSN 1175-5334 (online edition) Ants of the genus Lordomyrma Emery (1) Generic synonymy, composition and distribution, with notes on Ancyridris Wheeler and Cyphoidris Weber (Hymenoptera: Formicidae: Myrmicinae) ROBERT W. TAYLOR Australian National Insect Collection, CSIRO Division of Entomology, GPO Box 1700, Canberra City 2601, Australia. E-mail: [email protected] Abstract Synonymy under Lordomyrma of Prodicroaspis Emery and Promeranoplus Emery is reviewed. Lordomyrma currently comprises 25 named taxa, with two junior synonyms. Many undescribed species are known. Relative levels of species richness and morphological diversity are compared for the SE Asian/Japanese, Australian, Melanesian, New Caledonian and Fijian Lordomyrma faunas. Twelve species, including examples of the related genera Ancyridris and Cyphoidris are illustrated. The need for conservation and study of the remarkable, threatened ant faunas of New Caledonia, New Guinea and Fiji is discussed, and the relative positions of Ancyridris and Cyphoidris reviewed. Key words: Formicidae, evolution, speciation, species flocks, systematics, Japan, Southeast Asia, Australia, New Guinea, New Caledonia, Fiji, Africa Introduction Twenty-five valid named species are recognized here in the wonderfully diverse myrmicine genus Lor- domyrma Emery. Characteristics of these and approximately 40 undescribed species represented in the Aus- tralian National Insect Collection (ANIC) and elsewhere are discussed to evaluate the status of the genus, and to justify the synonymy under Lordomyrma of the nominal New Caledonian genera Prodicroaspis Emery and Promeranoplus Emery. The New Guinean genus Ancyridris and the Afrotropical Cyphoidris Weber are dis- cussed as putative relatives of Lordomyrma. -
The Venom Apparatus and Other Morphological Characters of the Ant Martialis Heureka (Hymenoptera, Formicidae, Martialinae)
Volume 50(26):413‑423, 2010 The venom apparaTus and oTher morphological characTers of The anT Martialis heureka (hymenopTera, formicidae, marTialinae) carlos roberTo ferrreira brandão1,3 Jorge luis machado diniz2 rodrigo dos sanTos machado feiTosa1 AbstrAct We describe and illustrate the venom apparatus and other morphological characters of the recently described Martialis heureka ant worker, a supposedly specialized subterranean predator which could be the sole surviving representative of a highly divergent lineage that arose near the dawn of ant diversification. M. heureka was described as the single species of a genus in the subfamily, Martialinae Rabeling and Verhaagh, known from a single worker. However because the authors had available a unique specimen, dissections and scanning electron microscopy from coated specimens were not possible. We base our study on two worker individuals collected in Manaus, AM, Brazil in 1998 and maintained in 70% alcohol since then; the ants were partially destroyed because of desiccation during transport to São Paulo and subsequent efforts to rescue them from the vial. We were able to recover two left mandibles, two pronota, one dismembered fore coxa, one meso-metapropodeal complex with the median and hind coxae and trochanters still attached, one postpetiole, two gastric tergites, the pygidium and the almost complete venom apparatus (lacking the gonostylus and anal plate). We illustrate and describe the pieces, and compare M. heureka worker morphology with other basal ant subfamilies, concluding it does merit subfamilial status. Keywords: Ant phylogeny; Formicidae; Martialis; Ultrastructure; Venom Apparatus. IntroductIon dusk in a primary lowland rainforest walking on the leaf litter. The ant Martialis heureka was recently described The phylogenetic position of this ant was inferred by Rabeling and Verhaagh (in Rabeling et al. -
Lab 19. Meiosis
Lab 19. Meiosis: How Does the Process of Meiosis Reduce the Number of Chromosomes in Reproductive Cells? Introduction Sexual reproduction is a process that creates a new organism by combining the genetic material of two organisms. There are two main steps in sexual reproduction: (1) the production of repro- ductive cells and (2) fertilization. Fertilization is the fusion of two reproductive cells to form a new individual. During fertilization, chromosomes from the male and female combine to form homologous pairs (see the figure below). The number of chromosomes donated from the male and female are equal, and offspring have the same number of chromosomes as each of the parents. A human karyotype depicting 23 homologous pairs of chromosomes. If the reproductive cell from a male and the reproductive cell from a female each donate the same number of chromosomes that are found in a typical cell to the new embryo, then the chromosome number of the species would double with each generation. Yet that doesn’t happen; the chromosome number within a species stays constant from one generation to the next. Therefore, a mechanism that reduces the number of chromosomes found in reproductive cells is needed to prevent the chromo- some number from doubling as the result of fertilization. This mechanism is called meiosis. It took many years of research and contributions from several different scientists to uncover what happens inside a cell during the complex process of meiosis. The German biologist Oscar Hertwig made the first major contribution in 1876, when he documented the stages of meiosis by examining the formation of eggs in sea urchins. -
Blanchard, B. D. & Moreau, C. S., Evolution
ORIGINAL ARTICLE doi:10.1111/evo.13117 Defensive traits exhibit an evolutionary trade-off and drive diversification in ants Benjamin D. Blanchard1,2,3 and Corrie S. Moreau2 1Committee on Evolutionary Biology, University of Chicago, Chicago, Illinois 60637 2Department of Science and Education, Integrative Research Center, Field Museum of Natural History, Chicago, Illinois 60605 3E-mail: bblanchard@fieldmuseum.org Received July 9, 2016 Accepted November 1, 2016 Evolutionary biologists have long predicted that evolutionary trade-offs among traits should constrain morphological divergence and species diversification. However, this prediction has yet to be tested in a broad evolutionary context in many diverse clades, including ants. Here, we reconstruct an expanded ant phylogeny representing 82% of ant genera, compile a new family-wide trait database, and conduct various trait-based analyses to show that defensive traits in ants do exhibit an evolutionary trade- off. In particular, the use of a functional sting negatively correlates with a suite of other defensive traits including spines, large eye size, and large colony size. Furthermore, we find that several of the defensive traits that trade off with a sting are also positively correlated with each other and drive increased diversification, further suggesting that these traits form a defensive suite. Our results support the hypothesis that trade-offs in defensive traits significantly constrain trait evolution and influence species diversification in ants. KEY WORDS: Ancestral state reconstruction, defense, evolutionary trade-off, Formicidae, trait-based diversification. All species experience constraints arising from developmental, Trait trade-offs influence various evolutionary processes, in- functional, and energetic limitations. These limitations have fea- cluding patterns of morphological divergence (DeWitt et al. -
Zootaxa, Ants of the Genus Lordomyrma Emery
Zootaxa 1979: 16–28 (2009) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2009 · Magnolia Press ISSN 1175-5334 (online edition) Ants of the genus Lordomyrma Emery (1) Generic synonymy, composition and distribution, with notes on Ancyridris Wheeler and Cyphoidris Weber (Hymenoptera: Formicidae: Myrmicinae) ROBERT W. TAYLOR Australian National Insect Collection, CSIRO Division of Entomology, GPO Box 1700, Canberra City 2601, Australia. E-mail: [email protected] Abstract Synonymy under Lordomyrma of Prodicroaspis Emery and Promeranoplus Emery is reviewed. Lordomyrma currently comprises 25 named taxa, with two junior synonyms. Many undescribed species are known. Relative levels of species richness and morphological diversity are compared for the SE Asian/Japanese, Australian, Melanesian, New Caledonian and Fijian Lordomyrma faunas. Twelve species, including examples of the related genera Ancyridris and Cyphoidris are illustrated. The need for conservation and study of the remarkable, threatened ant faunas of New Caledonia, New Guinea and Fiji is discussed, and the relative positions of Ancyridris and Cyphoidris reviewed. Key words: Formicidae, evolution, speciation, species flocks, systematics, Japan, Southeast Asia, Australia, New Guinea, New Caledonia, Fiji, Africa Introduction Twenty-five valid named species are recognized here in the wonderfully diverse myrmicine genus Lor- domyrma Emery. Characteristics of these and approximately 40 undescribed species represented in the Aus- tralian National Insect Collection (ANIC) and elsewhere are discussed to evaluate the status of the genus, and to justify the synonymy under Lordomyrma of the nominal New Caledonian genera Prodicroaspis Emery and Promeranoplus Emery. The New Guinean genus Ancyridris and the Afrotropical Cyphoidris Weber are dis- cussed as putative relatives of Lordomyrma. -
William Ernest Castle, American Geneticist
AN ABSTRACT OF THE THESIS OF H. Terry Taylor for the degree of Master of Arts in General Science (History of Science) presented onAugust 17, 1983 Title: William Ernest Castle: American Geneticist. A Case-Study in the Impact of the Mendelian Research Program Redacted for Privacy Abstract approved: In their modern context questions of heredity have come to be closely aligned with theories of evolution because all such theories require the presence of heritable variation. Thus the need for an understanding of a source of variation and a mechanism for its in- heritance became very apparent with the general acceptance of organic evolution among biologists in the 1870's. Yet no one theory of evolution or of heredity became generally accepted until the modern synthesis of the 1930's. This thesis ad- dresses the question of how this modern synthetic theory gained wide- spread acceptance and seeks to answer it by studying the development of a theory of heredity both before and after the rediscovery of Mendel ca. 1900. Those factors making possible the rediscovery in terms of the developments in heredity and evolution are treated as a background for the reception of Mendel. Theories discussed include those of Charles Darwin, August Weismann, Hugo de Vries and the American neo- Lamarckians. These theories also serve as a background against which to see the life and work of William Ernest Castle. This man was trained during the 1890's, receiving his Ph.D. under E.L. Mark at Harvard. In 1900 he became one of the very first to begin Mendelian experiments on animal material, working with small animals. -
Phylogeny and Biogeography of a Hyperdiverse Ant Clade (Hymenoptera: Formicidae)
UC Davis UC Davis Previously Published Works Title The evolution of myrmicine ants: Phylogeny and biogeography of a hyperdiverse ant clade (Hymenoptera: Formicidae) Permalink https://escholarship.org/uc/item/2tc8r8w8 Journal Systematic Entomology, 40(1) ISSN 0307-6970 Authors Ward, PS Brady, SG Fisher, BL et al. Publication Date 2015 DOI 10.1111/syen.12090 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Systematic Entomology (2015), 40, 61–81 DOI: 10.1111/syen.12090 The evolution of myrmicine ants: phylogeny and biogeography of a hyperdiverse ant clade (Hymenoptera: Formicidae) PHILIP S. WARD1, SEÁN G. BRADY2, BRIAN L. FISHER3 andTED R. SCHULTZ2 1Department of Entomology and Nematology, University of California, Davis, CA, U.S.A., 2Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC, U.S.A. and 3Department of Entomology, California Academy of Sciences, San Francisco, CA, U.S.A. Abstract. This study investigates the evolutionary history of a hyperdiverse clade, the ant subfamily Myrmicinae (Hymenoptera: Formicidae), based on analyses of a data matrix comprising 251 species and 11 nuclear gene fragments. Under both maximum likelihood and Bayesian methods of inference, we recover a robust phylogeny that reveals six major clades of Myrmicinae, here treated as newly defined tribes and occur- ring as a pectinate series: Myrmicini, Pogonomyrmecini trib.n., Stenammini, Solenop- sidini, Attini and Crematogastrini. Because we condense the former 25 myrmicine tribes into a new six-tribe scheme, membership in some tribes is now notably different, espe- cially regarding Attini. We demonstrate that the monotypic genus Ankylomyrma is nei- ther in the Myrmicinae nor even a member of the more inclusive formicoid clade – rather it is a poneroid ant, sister to the genus Tatuidris (Agroecomyrmecinae). -
Genome-Based, Mechanism-Driven Computational Modeling of Risks Of
2 K. Sankaranarayanan, H. Nikjoo / Mutation Research 764 (2015) 1–15 pregnancy outcomes (including stillbirths, neonatal deaths and 2. Uncertainties and unsolved problems Mutation Research 764 (2015) 1–15 congenital malformations in live births in phase I (1948–1954); Mutation Research 764 (2015) 1–15 sex-ratio shifts and survival of live-born infants in phase II (1955– Although the estimates presented in Table 1 reflect the state 1968); and cancers in F1 children, sex-chromosomal aneuploids, of the art in the field at the end of the 20th century, several Contents lists available at ScienceDirect balanced structural rearrangements and mutations affecting uncertainties and unsolved problems remain. These have been Genome-based, mechanism-driven computational protein charge or function in phase III (1969–1990) (reviewed discussed in detail elsewhere [7–9]. In what follows, we briefly in [5]). Of note is that these studies were not aimed at detecting address three of the most obvious ones, namely, (a) the Mutation Research/Reviews in Mutation Research possible increases in the frequencies of children affected by doubling dose method of risk estimation itself; (b) inability to modeling of risks of ionizing radiation: radiation-induced genetic diseases. Reports of progress in these define the genetic radiosensitivity of human females and (c) jo urnal homepage: www.elsevier.com/locate/reviewsmr studies published from time to time until 1998 [6] provided no lack of evidence for radiation-induced genetic disease in Co mmunity address: www.elsevier.com/locate/mutres ☆, ☆ ☆ The next frontier in genetic risk estimation? evidence of any detectable increase in adverse effects (as humans. -
Colony Size Evolution in Ants: Macroevolutionary Trends
Insect. Soc. (2016) 63:291–298 DOI 10.1007/s00040-016-0465-3 Insectes Sociaux RESEARCH ARTICLE Colony size evolution in ants: macroevolutionary trends 1,2 1 A. T. Burchill • C. S. Moreau Received: 27 October 2015 / Revised: 11 January 2016 / Accepted: 14 January 2016 / Published online: 5 February 2016 Ó International Union for the Study of Social Insects (IUSSI) 2016 Abstract Colony size is an incredibly important factor in Keywords Formicidae Á Eusociality Á social insect ecology: it affects everything from foraging Comparative methods Á Phylogenetics Á MuSSE Á strategies to colony defense to mating systems to the degree Colony size Á Group size of polymorphism. However, colony sizes vary dramatically among ant species (Formicidae): sizes range from several workers living together to super-colonies that stretch for Introduction hundreds of kilometers. Although the origins of eusociality and colonial life have been extensively theorized, little work The theoretical origin of eusociality in insects is a well- has been done describing the evolution of colony size that discussed topic in biology (Wilson 1971; Oster and Wilson followed after. Our study provides the first large-scale 1978; Crozier and Pamilo 1996). There are multiple possi- investigation into such issues, incorporating colony size ble theoretical routes to eusociality in Hymenoptera (bees, data from 118 genera and recently published, nearly com- wasps, and ants), and the specific models continue to be plete genus-level molecular phylogenies. We find that debated (Wilson 2008; Hughes et al. 2008; Abbot et al. colony size change exhibits a bifurcation pattern similar to 2011; Nowak et al. 2010).