Reproduction in Protists
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											A Comparison of Pollinator Limitation, Self-Compatibility, and Inbreeding Depression.In Populations of Campanula Rotundifolia Lm A Comparison of Pollinator Limitation, Self-compatibility, and Inbreeding Depression.in Populations of Campanula rotundifolia L. (Campanulaceae) at Elevational Extremes Final Report Submitted to: The City of Boulder Open Space and Mountain Parks Research/Monitoring Program Robin A. Bingham and Keri L. Howe Department of Environmental, Population and Organismic Biology The University of Colorado Boulder, Colorado Abstract Campanula rotundifolia is a widespread herbaceous perennial that exists along an elevational gradient in Colorado. Alpine populations of this and other insect pollinated species may suffer from pollinator limitation due to the harsh environment of high elevations. Limited gene flow due to low levels of pol1inator.activitymay increase rates of selfing and biparental inbreeding in alpine populations. This could result in highly inbred populations that have been purged of deleterious recessive alleles and, therefore, may exhibit less inbreeding depression than primarily outcrossed populations of the same species from lower elevations. We determined the levels of inbreeding depression and self-compatibility in high and low-elevation populations of C. rotundifolia. Hand self- and outcross-pollinations were performed on plants at high and low elevations. Seed set was determined to assess levels of self-compatibility. Seeds were weighed, germinated, and grown in a common garden to determine levels of inbreeding depression. Plants in la all populations were found to be self-compatible, and capable of autogamous seed set. Although visitation rates in the high-elevation population were significantly lower that in low elevation populations, there was no evidence for pollinator limitation in alpine populations. Low-elevation seedlings exhibited significant inbreeding depression for all parameters measured, while the high-elevation seedlings did not.
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												  Reproductive Assurance Through Autogamous Self-Pollination Across Diverse Sexual and Breeding SystemsView metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by ePrints@ATREE REVIEW ARTICLE Reproductive assurance through autogamous self-pollination across diverse sexual and breeding systems K. R. Shivanna* Ashoka Trust for Research in Ecology and the Environment, Royal Enclave, Srirampura, Jakkur Post, Bengaluru 560 064, India the development of functional pollen grains and ovules, Pollination becomes a constraint when conspecific plants and/or their pollinators become scarce. Many and terminating in seed development. Pollination, deposi- plant species have evolved autogamous self-pollination tion of the pollen grains from the anther onto the stigma, as a means of reproductive assurance (RA) under is one of the most critical requirements and determines, to pollination-uncertain environments. So far RA has a large extent, reproductive success of the species. As been studied and discussed largely with reference to plants are stationary, they have to depend on external self-compatible species producing bisexual flowers. agents for pollination services. Nearly 90% of the plants RA seems to have evolved across all other sexual and depend on animals for pollination and the remaining on breeding systems – monoecy, dioecy and self-incom- wind or water1. Pollination success depends not only on patibility (SI). Both monoecy and dioecy produce the number but also the type of pollen grains deposited on bisexual flowers (andro/gyno-monoecy, andro/gyno- the stigma. This number has to be adequate to initiate dioecy and polygamous conditions) which may fruit development and pollen grains have to be of com- provide RA. Similarly, most of the SI species are leaky and do set some seeds upon self-pollination.
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												  “Salivary Gland Cellular Architecture in the Asian Malaria Vector Mosquito Anopheles Stephensi”Wells and Andrew Parasites & Vectors (2015) 8:617 DOI 10.1186/s13071-015-1229-z RESEARCH Open Access “Salivary gland cellular architecture in the Asian malaria vector mosquito Anopheles stephensi” Michael B. Wells and Deborah J. Andrew* Abstract Background: Anopheles mosquitoes are vectors for malaria, a disease with continued grave outcomes for human health. Transmission of malaria from mosquitoes to humans occurs by parasite passage through the salivary glands (SGs). Previous studies of mosquito SG architecture have been limited in scope and detail. Methods: We developed a simple, optimized protocol for fluorescence staining using dyes and/or antibodies to interrogate cellular architecture in Anopheles stephensi adult SGs. We used common biological dyes, antibodies to well-conserved structural and organellar markers, and antibodies against Anopheles salivary proteins to visualize many individual SGs at high resolution by confocal microscopy. Results: These analyses confirmed morphological features previously described using electron microscopy and uncovered a high degree of individual variation in SG structure. Our studies provide evidence for two alternative models for the origin of the salivary duct, the structure facilitating parasite transport out of SGs. We compare SG cellular architecture in An. stephensi and Drosophila melanogaster, a fellow Dipteran whose adult SGs are nearly completely unstudied, and find many conserved features despite divergence in overall form and function. Anopheles salivary proteins previously observed at the basement membrane were localized either in SG cells, secretory cavities, or the SG lumen. Our studies also revealed a population of cells with characteristics consistent with regenerative cells, similar to muscle satellite cells or midgut regenerative cells. Conclusions: This work serves as a foundation for linking Anopheles stephensi SG cellular architecture to function and as a basis for generating and evaluating tools aimed at preventing malaria transmission at the level of mosquito SGs.
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												  Evolutionary Pathways to Self-Fertilization in a Tristylous PlantReview BlackwellOxford,NPHNew0028-646X1469-8137©293710.1111/j.1469-8137.2009.02937.xJune0546???556???ResearchXX The 2009Phytologist Authors UK Review Publishing (2009). Ltd Journal compilation © New Phytologist (2009) Research reviewXX Evolutionary pathways to self- fertilization in a tristylous plant species Author for correspondence: Spencer C. H. Barrett, Rob W. Ness and Mario Vallejo-Marín Spencer C. H. Barrett Department of Ecology and Evolutionary Biology, University of Toronto, 25 Willcocks St, Toronto, Tel: +1 416 978 5603 Email: [email protected] Ontario, Canada, M5S 3B2 Received: 23 April 2009 Accepted: 20 May 2009 Summary New Phytologist (2009) 183: 546–556 Evolutionary transitions from outcrossing to selfing occur commonly in heterostylous doi: 10.1111/j.1469-8137.2009.02937.x genera. The morphological polymorphisms that characterize heterostyly provide opportunities for different pathways for selfing to evolve. Here, we investigate the Key words: developmental instability, origins and pathways by which selfing has evolved in tristylous Eichhornia paniculata Eichhornia, herkogamy, heterostyly, multiple by providing new evidence based on morphology, DNA sequences and genetic analysis. origins, pathways to self-fertilization. The primary pathway from outcrossing to selfing involves the stochastic loss of the short-styled morph (S-morph) from trimorphic populations, followed by the spread of selfing variants of the mid-styled morph (M-morph). However, the discovery of selfing variants of the long-styled morph (L-morph) in Central America indicates a secondary pathway and distinct origin for selfing. Comparisons of multi-locus nucleo- tide sequences from 27 populations sampled from throughout the geographical range suggest multiple transitions to selfing. Genetic analysis of selfing variants of the L- and M-morphs demonstrates recessive control of the loss of herkogamy, although the number of factors appears to differ between the forms.
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												  Genetic Diversity and Reproductive Biology in Warea Carteri (Brassicaceae), a Narrowly Endemic Florida Scrub Annual Author(S): Margaret EGenetic Diversity and Reproductive Biology in Warea carteri (Brassicaceae), a Narrowly Endemic Florida Scrub Annual Author(s): Margaret E. K. Evans, Rebecca W. Dolan, Eric S. Menges, Doria R. Gordon Source: American Journal of Botany, Vol. 87, No. 3 (Mar., 2000), pp. 372-381 Published by: Botanical Society of America Stable URL: http://www.jstor.org/stable/2656633 . Accessed: 22/10/2011 09:41 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Botanical Society of America is collaborating with JSTOR to digitize, preserve and extend access to American Journal of Botany. http://www.jstor.org AmericanJournal of Botany 87(3): 372-381. 2000. GENETIC DIVERSITY AND REPRODUCTIVE BIOLOGY IN WAREA CARTERI (BRASSICACEAE), A NARROWLY ENDEMIC FLORIDA SCRUB ANNUAL1 MARGARET E. K. EVANS,25 REBECCA W. DOLAN,3 ERIC S. MENGES,2 AND DORIA R. GORDON4 2ArchboldBiological Station,PO. Box 2057, Lake Placid, Florida 33862 USA; 3FriesnerHerbarium, Butler University,Indianapolis, Indiana 46208 USA; and 4The Nature Conservancy,Department of Botany,PO. Box 118526, Universityof Florida, Gainesville, Florida 32611 USA Carter's mustard(Warea carteri) is an endangered,fire-stimulated annual endemic of the Lake Wales Ridge, Florida, USA. This species is characterizedby seed banks and large fluctuationsin plant numbers,with increases occurringin postdisturbancehabitat.
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												  The Intestinal ProtozoaThe Intestinal Protozoa A. Introduction 1. The Phylum Protozoa is classified into four major subdivisions according to the methods of locomotion and reproduction. a. The amoebae (Superclass Sarcodina, Class Rhizopodea move by means of pseudopodia and reproduce exclusively by asexual binary division. b. The flagellates (Superclass Mastigophora, Class Zoomasitgophorea) typically move by long, whiplike flagella and reproduce by binary fission. c. The ciliates (Subphylum Ciliophora, Class Ciliata) are propelled by rows of cilia that beat with a synchronized wavelike motion. d. The sporozoans (Subphylum Sporozoa) lack specialized organelles of motility but have a unique type of life cycle, alternating between sexual and asexual reproductive cycles (alternation of generations). e. Number of species - there are about 45,000 protozoan species; around 8000 are parasitic, and around 25 species are important to humans. 2. Diagnosis - must learn to differentiate between the harmless and the medically important. This is most often based upon the morphology of respective organisms. 3. Transmission - mostly person-to-person, via fecal-oral route; fecally contaminated food or water important (organisms remain viable for around 30 days in cool moist environment with few bacteria; other means of transmission include sexual, insects, animals (zoonoses). B. Structures 1. trophozoite - the motile vegetative stage; multiplies via binary fission; colonizes host. 2. cyst - the inactive, non-motile, infective stage; survives the environment due to the presence of a cyst wall. 3. nuclear structure - important in the identification of organisms and species differentiation. 4. diagnostic features a. size - helpful in identifying organisms; must have calibrated objectives on the microscope in order to measure accurately.
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												  Oecd Guideline for the Testing of Chemicals474 Adopted: 21st July 1997 OECD GUIDELINE FOR THE TESTING OF CHEMICALS Mammalian Erythrocyte Micronucleus Test INTRODUCTION 1. The mammalian in vivo micronucleus test is used for the detection of damage induced by the test substance to the chromosomes or the mitotic apparatus of erythroblasts by analysis of erythrocytes as sampled in bone marrow and/or peripheral blood cells of animals, usually rodents. 2. The purpose of the micronucleus test is to identify substances that cause cytogenetic damage which results in the formation of micronuclei containing lagging chromosome fragments or whole chromosomes. 3. When a bone marrow erythroblast develops into a polychromatic erythrocyte, the main nucleus is extruded; any micronucleus that has been formed may remain behind in the otherwise anucleated cytoplasm. Visualisation of micronuclei is facilitated in these cells because they lack a main nucleus. An increase in the frequency of micronucleated polychromatic erythrocytes in treated animals is an indication of induced chromosome damage. 4. Definitions used are set out in the Annex. INITIAL CONSIDERATIONS 5. The bone marrow of rodents is routinely used in this test since polychromatic erythrocytes are produced in that tissue. The measurement of micronucleated immature (polychromatic) erythrocytes in peripheral blood is equally acceptable in any species in which the inability of the spleen to remove micronucleated erythrocytes has been demonstrated, or which has shown an adequate sensitivity to detect agents that cause structural or numerical chromosome aberrations. Micronuclei can be distinguished by a number of criteria. These include identification of the presence or absence of a kinetochore or centromeric DNA in the micronuclei. The frequency of micronucleated immature (polychromatic) erythrocytes is the principal endpoint.
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												  S2(R1) Genotoxicity Testing and Data Interpretation for Pharmaceuticals Intended for Human UseGuidance for Industry S2(R1) Genotoxicity Testing and Data Interpretation for Pharmaceuticals Intended for Human Use U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for Biologics Evaluation and Research (CBER) June 2012 ICH Guidance for Industry S2(R1) Genotoxicity Testing and Data Interpretation for Pharmaceuticals Intended for Human Use Additional copies are available from: Office of Communications Division of Drug Information, WO51, Room 2201 Center for Drug Evaluation and Research Food and Drug Administration 10903 New Hampshire Ave., Silver Spring, MD 20993-0002 Phone: 301-796-3400; Fax: 301-847-8714 [email protected] http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm and/or Office of Communication, Outreach and Development, HFM-40 Center for Biologics Evaluation and Research Food and Drug Administration 1401 Rockville Pike, Rockville, MD 20852-1448 http://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Guidances/default.htm (Tel) 800-835-4709 or 301-827-1800 U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for Biologics Evaluation and Research (CBER) June 2012 ICH Contains Nonbinding Recommendations TABLE OF CONTENTS I. INTRODUCTION (1)....................................................................................................... 1 A. Objectives of the Guidance (1.1)...................................................................................................1
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												  Biology Chapter 19 Kingdom Protista Domain Eukarya Description Kingdom Protista Is the Most Diverse of All the KingdomsBiology Chapter 19 Kingdom Protista Domain Eukarya Description Kingdom Protista is the most diverse of all the kingdoms. Protists are eukaryotes that are not animals, plants, or fungi. Some unicellular, some multicellular. Some autotrophs, some heterotrophs. Some with cell walls, some without. Didinium protist devouring a Paramecium protist that is longer than it is! Read about it on p. 573! Where Do They Live? • Because of their diversity, we find protists in almost every habitat where there is water or at least moisture! Common Examples • Ameba • Algae • Paramecia • Water molds • Slime molds • Kelp (Sea weed) Classified By: (DON’T WRITE THIS DOWN YET!!! • Mode of nutrition • Cell walls present or not • Unicellular or multicellular Protists can be placed in 3 groups: animal-like, plantlike, or funguslike. Didinium, is a specialist, only feeding on Paramecia. They roll into a ball and form cysts when there is are no Paramecia to eat. Paramecia, on the other hand are generalists in their feeding habits. Mode of Nutrition Depends on type of protist (see Groups) Main Groups How they Help man How they Hurt man Ecosystem Roles KEY CONCEPT Animal-like protists = PROTOZOA, are single- celled heterotrophs that can move. Oxytricha Reproduce How? • Animal like • Unicellular – by asexual reproduction – Paramecium – does conjugation to exchange genetic material Animal-like protists Classified by how they move. macronucleus contractile vacuole food vacuole oral groove micronucleus cilia • Protozoa with flagella are zooflagellates. – flagella help zooflagellates swim – more than 2000 zooflagellates • Some protists move with pseudopods = “false feet”. – change shape as they move –Ex. amoebas • Some protists move with pseudopods.
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												  The Protozoan Nucleus. Molecular and Biochemical Parasitology, 209(1-2), PpMcCulloch, R., and Navarro, M. (2016) The protozoan nucleus. Molecular and Biochemical Parasitology, 209(1-2), pp. 76-87. (doi:10.1016/j.molbiopara.2016.05.002) This is the author’s final accepted version. There may be differences between this version and the published version. You are advised to consult the publisher’s version if you wish to cite from it. http://eprints.gla.ac.uk/135296/ Deposited on: 22 February 2017 Enlighten – Research publications by members of the University of Glasgow http://eprints.gla.ac.uk *Manuscript Click here to view linked References The protozoan nucleus Richard McCulloch1 and Miguel Navarro2 1. The Wellcome Trust Centre for Molecular Parasitology, Institute of Infection, Immunity and Inflammation, University of Glasgow, Sir Graeme Davis Building, 120 University Place, Glasgow, G12 8TA, U.K. Telephone: 01413305946 Fax: 01413305422 Email: [email protected] 2. Instituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas (CSIC), Avda. del Conocimiento s/n, 18100 Granada, Spain. Email: [email protected] Correspondence can be sent to either of above authors Keywords: nucleus; mitosis; nuclear envelope; chromosome; DNA replication; gene expression; nucleolus; expression site body 1 Abstract The nucleus is arguably the defining characteristic of eukaryotes, distinguishing their cell organisation from both bacteria and archaea. Though the evolutionary history of the nucleus remains the subject of debate, its emergence differs from several other eukaryotic organelles in that it appears not to have evolved through symbiosis, but by cell membrane elaboration from an archaeal ancestor. Evolution of the nucleus has been accompanied by elaboration of nuclear structures that are intimately linked with most aspects of nuclear genome function, including chromosome organisation, DNA maintenance, replication and segregation, and gene expression controls.
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												  Extraordinary Genome Stability in the Ciliate Paramecium TetraureliaExtraordinary genome stability in the ciliate Paramecium tetraurelia Way Sunga,1, Abraham E. Tuckera, Thomas G. Doaka, Eunjin Choia, W. Kelley Thomasb, and Michael Lyncha aDepartment of Biology, Indiana University, Bloomington, IN 47405; and bDepartment of Molecular Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH 03824 Edited by Detlef Weigel, Max Planck Institute for Developmental Biology, Tübingen, Germany, and approved October 10, 2012 (received for review June 21, 2012) Mutation plays a central role in all evolutionary processes and is also from this experiment), or ∼30–50 fissions when starved (9), P. the basis of genetic disorders. Established base-substitution muta- tetraurelia undergoes a self-fertilization process known as au- tion rates in eukaryotes range between ∼5 × 10−10 and 5 × 10−8 per togamy (9), at which time the old macronucleus is destroyed and site per generation, but here we report a genome-wide estimate for replaced by a processed version of the new micronuclear genome Paramecium tetraurelia that is more than an order of magnitude (10). When in contact with compatible mating types, P. tetraurelia lower than any previous eukaryotic estimate. Nevertheless, when can also undergo conjugation (10), although, this can be pre- the mutation rate per cell division is extrapolated to the length of vented in the laboratory by using a stock consisting of only one the sexual cycle for this protist, the measure obtained is comparable mating type. Under conditions of exclusive autogamy, all muta- to that for multicellular species with similar genome sizes. Because tions arising in the micronucleus during clonal propagation Paramecium has a transcriptionally silent germ-line nucleus, these should accumulate in a completely neutral fashion, with the fit- results are consistent with the hypothesis that natural selection ness effects only being realized after sexual reproduction.
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												  Somatic Deleterious Mutation Rate in a Woody Plant: Estimation from Phenotypic DataHeredity (2013) 111, 338–344 & 2013 Macmillan Publishers Limited All rights reserved 0018-067X/13 www.nature.com/hdy ORIGINAL ARTICLE Somatic deleterious mutation rate in a woody plant: estimation from phenotypic data K Bobiwash1,3, ST Schultz2,3 and DJ Schoen1 We conducted controlled crosses in populations of the long-lived clonal shrub, Vaccinium angustifolium (lowbush blueberry) to estimate inbreeding depression and mutation parameters associated with somatic deleterious mutation. Inbreeding depression level was high, with many plants failing to set fruit after self-pollination. We also compared fruit set from autogamous pollinations (pollen collected from within the same inflorescence) with fruit set from geitonogamous pollinations (pollen collected from the same plant but from inflorescences separated by several meters of branch growth). The difference between geitonogamous versus autogamous fitness within single plants is referred to as ‘autogamy depression’ (AD). AD can be caused by somatic deleterious mutation. AD was significantly different from zero for fruit set. We developed a maximum-likelihood procedure to estimate somatic mutation parameters from AD, and applied it to geitonogamous and autogamous fruit set data from this experiment. We infer that, on average, approximately three sublethal, partially dominant somatic mutations exist within the crowns of the plants studied. We conclude that somatic mutation in this woody plant results in an overall genomic deleterious mutation rate that exceeds the rate measured to date for annual plants. Some implications of this result for evolutionary biology and agriculture are discussed. Heredity (2013) 111, 338–344; doi:10.1038/hdy.2013.57; published online 19 June 2013 Keywords: somatic mutation; deleterious mutation; inbreeding depression; long-lived plants INTRODUCTION meristems divide to produce additional stem cells and somatic tissue Plants violate the Weismann’s doctrine of the separation of germ line (Klekowski et al., 1985; Pineda-Krch and Lehtila, 2002).