The Germ-Plasm: a Theory of Heredity (1893), by August Weismann [1]
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Monism and Morphology at the Turn of the Twentieth Century
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by IUScholarWorks From a draft. May differ from the published version, which appeared in Monism: Science, Philosophy, Religion, and the History of a Worldview, ed. Todd Weir, 135–158, New York: Palgrave USA, 2012. Monism and Morphology at the Turn of the Twentieth Century SANDER GLIBOFF Indiana University Abstract. Ernst Haeckel’s monistic worldview and his interpretation of Darwin’s theory of evolution worked together to help him rule out any role for divine providence or any non-material mind, spirit, will, or purpose in the organic world. In his account of 1866, the impersonal, unpredictable, and purposeless external environment was what drove evolutionary change. By around the turn of the twentieth century, however, new theories of evolution, heredity, and embryology were challenging Haeckel’s, but Haeckel no longer responded with his earlier vigor. Younger monistically oriented evolutionary biologists had to take the lead in modernizing and defending the monistic interpretation and the external causes of evolution. Three of these younger biologists are discussed here: Haeckel’s student, the morphologist-turned-theoretician Richard Semon (1859–1918); Ludwig Plate (1862–1937), who took over Haeckel’s chair at the University of Jena and became an influential journal editor and commentator on new research on heredity and evolution; and Paul Kammerer (1880–1926), whose experimental evidence for the modifying power of the environment was hotly debated. Despite their very different social, political, and religious backgrounds, their contrasting research methods and career trajectories, and their disagreements on the precise mechanisms of evolution, these three were united by their adherence to Haeckelian monistic principles. -
Metazoan Ribosome Inactivating Protein Encoding Genes Acquired by Horizontal Gene Transfer Received: 30 September 2016 Walter J
www.nature.com/scientificreports OPEN Metazoan Ribosome Inactivating Protein encoding genes acquired by Horizontal Gene Transfer Received: 30 September 2016 Walter J. Lapadula1, Paula L. Marcet2, María L. Mascotti1, M. Virginia Sanchez-Puerta3 & Accepted: 5 April 2017 Maximiliano Juri Ayub1 Published: xx xx xxxx Ribosome inactivating proteins (RIPs) are RNA N-glycosidases that depurinate a specific adenine residue in the conserved sarcin/ricin loop of 28S rRNA. These enzymes are widely distributed among plants and their presence has also been confirmed in several bacterial species. Recently, we reported for the first timein silico evidence of RIP encoding genes in metazoans, in two closely related species of insects: Aedes aegypti and Culex quinquefasciatus. Here, we have experimentally confirmed the presence of these genes in mosquitoes and attempted to unveil their evolutionary history. A detailed study was conducted, including evaluation of taxonomic distribution, phylogenetic inferences and microsynteny analyses, indicating that mosquito RIP genes derived from a single Horizontal Gene Transfer (HGT) event, probably from a cyanobacterial donor species. Moreover, evolutionary analyses show that, after the HGT event, these genes evolved under purifying selection, strongly suggesting they play functional roles in these organisms. Ribosome inactivating proteins (RIPs, EC 3.2.2.22) irreversibly modify ribosomes through the depurination of an adenine residue in the conserved alpha-sarcin/ricin loop of 28S rRNA1–4. This modification prevents the binding of elongation factor 2 to the ribosome, arresting protein synthesis5, 6. The occurrence of RIP genes has been exper- imentally confirmed in a wide range of plant taxa, as well as in several species of Gram positive and Gram negative bacteria7–9. -
The Medical & Scientific Library of W. Bruce
The Medical & Scientific Library of W. Bruce Fye New York I March 11, 2019 The Medical & Scientific Library of W. Bruce Fye New York | Monday March 11, 2019, at 10am and 2pm BONHAMS LIVE ONLINE BIDDING IS INQUIRIES CLIENT SERVICES 580 Madison Avenue AVAILABLE FOR THIS SALE New York Monday – Friday 9am-5pm New York, New York 10022 Please email bids.us@bonhams. Ian Ehling +1 (212) 644 9001 www.bonhams.com com with “Live bidding” in Director +1 (212) 644 9009 fax the subject line 48 hrs before +1 (212) 644 9094 PREVIEW the auction to register for this [email protected] ILLUSTRATIONS Thursday, March 7, service. Front cover: Lot 188 10am to 5pm Tom Lamb, Director Inside front cover: Lot 53 Friday, March 8, Bidding by telephone will only be Business Development Inside back cover: Lot 261 10am to 5pm accepted on a lot with a lower +1 (917) 921 7342 Back cover: Lot 361 Saturday, March 9, estimate in excess of $1000 [email protected] 12pm to 5pm REGISTRATION Please see pages 228 to 231 Sunday, March 10, Darren Sutherland, Specialist IMPORTANT NOTICE for bidder information including +1 (212) 461 6531 12pm to 5pm Please note that all customers, Conditions of Sale, after-sale [email protected] collection and shipment. All irrespective of any previous activity SALE NUMBER: 25418 with Bonhams, are required to items listed on page 231, will be Tim Tezer, Junior Specialist complete the Bidder Registration transferred to off-site storage +1 (917) 206 1647 CATALOG: $35 Form in advance of the sale. -
'Great Is Darwin and Bergson His Poet': Julian Huxley's Other
This is a repository copy of ‘Great is Darwin and Bergson his poet’: Julian Huxley's other evolutionary synthesis. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/124449/ Version: Accepted Version Article: Herring, E (2018) ‘Great is Darwin and Bergson his poet’: Julian Huxley's other evolutionary synthesis. Annals of Science, 75 (1). pp. 40-54. ISSN 0003-3790 https://doi.org/10.1080/00033790.2017.1407442 (c) 2018 Informa UK Limited, trading as Taylor & Francis Group. This is an Accepted Manuscript of an article published by Taylor & Francis in Annals of Science on 04 Jan 2018, available online: http://www.tandfonline.com/10.1080/00033790.2017.1407442 Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ “Great is Darwin and Bergson his poet”: Julian Huxley’s Other Evolutionary Synthesis. Emily Herring School of Philosophy, Religion and History of Science, University of Leeds, Leeds, United Kingdom Email: [email protected] Address: School of Philosophy, Religion and History of Science, University of Leeds, Woodhouse Lane, Leeds, LS2 9JT, United Kingdom Orcid id: orcid.org/0000-0002-8377-6319 1 “Great is Darwin and Bergson his poet”: Julian Huxley’s Other Evolutionary Synthesis. -
Is the Germline Immortal and Continuous? a Discussion in Light of Ipscs and Germline Regeneration
Is the Germline Immortal and Continuous? A Discussion in Light of iPSCs and Germline Regeneration 1 1 Kate MacCord and B. Duygu Özpolat 1 - Marine Biological Laboratory, Woods Hole, MA, USA 1 ABSTRACT The germline gives rise to gametes, is the hereditary cell lineage, and is often called immortal and continuous. However, what exactly is immortal and continuous about the germline has recently come under scrutiny. The notion of an immortal and continuous germline has been around for over 130 years, and has led to the concept of a barrier between the germline and soma (the “Weismann barrier”). One repercussion of such a barrier is the understanding that when the germline is lost, soma cannot replace it, rendering the organism infertile. Recent research on induced pluripotent stem cells (iPSCs) and germline regeneration raise questions about the impermeability of the Weismann barrier and the designation of the germline as immortal and continuous. How we conceive of the germline and its immortality shapes what we perceive to be possible in animal biology, such as whether somatic cells contribute to the germline in some metazoans during normal development or regeneration. We argue that reassessing the universality of germline immortality and continuity across all metazoans leads to big and exciting open questions about the germ-soma cell distinction, cell reprogramming, germline editing, and even evolution. 2 1.0 Introduction The germline is the lineage of reproductive cells that includes gametes and their precursors, including primordial germ cells and germline stem cells. Because the germline gives rise to the gametes, it is the hereditary cell lineage, and is ultimately responsible for all cells in an organism’s body, including the next generation of the germline, stem cells, and other somatic cells. -
Reticulate Evolution Everywhere
Reticulate Evolution Everywhere Nathalie Gontier Abstract Reticulation is a recurring evolutionary pattern found in phylogenetic reconstructions of life. The pattern results from how species interact and evolve by mechanisms and processes including symbiosis; symbiogenesis; lateral gene transfer (that occurs via bacterial conjugation, transformation, transduction, Gene Transfer Agents, or the movements of transposons, retrotransposons, and other mobile genetic elements); hybridization or divergence with gene flow; and infec- tious heredity (induced either directly by bacteria, bacteriophages, viruses, pri- ons, protozoa and fungi, or via vectors that transmit these pathogens). Research on reticulate evolution today takes on inter- and transdisciplinary proportions and is able to unite distinct research fields ranging from microbiology and molecular genetics to evolutionary biology and the biomedical sciences. This chapter sum- marizes the main principles of the diverse reticulate evolutionary mechanisms and situates them into the chapters that make up this volume. Keywords Reticulate evolution · Symbiosis · Symbiogenesis · Lateral Gene Transfer · Infectious agents · Microbiome · Viriome · Virolution · Hybridization · Divergence with gene flow · Evolutionary patterns · Extended Synthesis 1 Reticulate Evolution: Patterns, Processes, Mechanisms According to the Online Etymology Dictionary (http://www.etymonline.com), the word reticulate is an adjective that stems from the Latin words “re¯ticulātus” (having a net-like pattern) and re¯ticulum (little net). When scholars identify the evolution of life as being “reticulated,” they first and foremost refer to a recurring evolutionary pattern. N. Gontier (*) AppEEL—Applied Evolutionary Epistemology Lab, University of Lisbon, Lisbon, Portugal e-mail: [email protected] © Springer International Publishing Switzerland 2015 1 N. Gontier (ed.), Reticulate Evolution, Interdisciplinary Evolution Research 3, DOI 10.1007/978-3-319-16345-1_1 2 N. -
Reader 19 05 19 V75 Timeline Pagination
Plant Trivia TimeLine A Chronology of Plants and People The TimeLine presents world history from a botanical viewpoint. It includes brief stories of plant discovery and use that describe the roles of plants and plant science in human civilization. The Time- Line also provides you as an individual the opportunity to reflect on how the history of human interaction with the plant world has shaped and impacted your own life and heritage. Information included comes from secondary sources and compila- tions, which are cited. The author continues to chart events for the TimeLine and appreciates your critique of the many entries as well as suggestions for additions and improvements to the topics cov- ered. Send comments to planted[at]huntington.org 345 Million. This time marks the beginning of the Mississippian period. Together with the Pennsylvanian which followed (through to 225 million years BP), the two periods consti- BP tute the age of coal - often called the Carboniferous. 136 Million. With deposits from the Cretaceous period we see the first evidence of flower- 5-15 Billion+ 6 December. Carbon (the basis of organic life), oxygen, and other elements ing plants. (Bold, Alexopoulos, & Delevoryas, 1980) were created from hydrogen and helium in the fury of burning supernovae. Having arisen when the stars were formed, the elements of which life is built, and thus we ourselves, 49 Million. The Azolla Event (AE). Hypothetically, Earth experienced a melting of Arctic might be thought of as stardust. (Dauber & Muller, 1996) ice and consequent formation of a layered freshwater ocean which supported massive prolif- eration of the fern Azolla. -
The Lamarckian Chicken and the Darwinian Egg Yitzhak Pilpel1* and Oded Rechavi2*
Pilpel and Rechavi Biology Direct (2015) 10:34 DOI 10.1186/s13062-015-0062-9 COMMENT Open Access The Lamarckian chicken and the Darwinian egg Yitzhak Pilpel1* and Oded Rechavi2* Abstract: “Which came first, the Chicken or the Egg?” We suggest this question is not a paradox. The Modern Synthesis envisions speciation through genetic changes in germ cells via random mutations, an “Egg first” scenario, but perhaps epigenetic inheritance mechanisms can transmit adaptive changes initiated in the soma (“Chicken first”). Reviewers: The article was reviewed by Dr. Eugene Koonin, Dr. Itai Yanai, Dr. Laura Landweber. Keywords: Evolution, Darwinian Evolution, Lamarckian Evolution, Modern Synthesis, Weismann Barrier, Epigenetic Inheritance, Transgenerational RNA Interference Background solution. Nevertheless, it is important to discuss why this In this commentary paper we wish to use the well- question is perceived as being paradoxical, and to exam- known “Chicken and Egg” paradox as a gateway for ine the true mystery that it holds; at the base of this discussing different processes of evolution. While in the dilemma stands an extremely important and unsolved biological sense this is not a paradox at all, the metaphor biological question: “Can the phenotype affect the is still useful because it allows examining of the distinc- genotype”? or put differently, “Can epigenetics translate tion between Lamarckian and Darwinian evolution, and into genetics”? specifically, since it enables us to raise an important and Asking the question in this manner allows mapping of unsolved question: “Can the phenotype affect the geno- the “Egg first” vs. the “Chicken first” options onto the type?” or in other words, “can epigenetics translate into distinction between Darwinian and Lamarckian evolu- genetics”? tion. -
Advances in Photosynthesis and Respiration, Volume 23: Structure and Function of Plastids
Photosynth Res (2006) 89:173–177 DOI 10.1007/s11120-006-9070-z ANNOUNCEMENT Advances in Photosynthesis and Respiration, Volume 23: Structure and Function of Plastids Govindjee Published online: 8 July 20061 Ó Springer Science+Business Media B.V. 2006 I am delighted to announce the publication, in Ad- Volume1: Molecular Biology of Cyanobacteria (28 vances in Photosynthesis and Respiration (AIPH) Chapters; 881 pages; 1994; edited by Donald A. Bryant, Series, of The Structure and Function of Plastids,a from USA; ISBN: 0-7923-3222-9); book covering the central role of plastids for life on Volume 2: Anoxygenic Photosynthetic Bacteria (62 earth. It deals with both the structure and the func- Chapters; 1331 pages; 1995; edited by Robert tion of these unique organelles, particularly of chlo- E. Blankenship, Michael T. Madigan, and Carl E. roplasts. Two distinguished authorities have edited Bauer, from USA; ISBN: 0-7923-3682-8); this volume: Robert R. Wise of the University of Volume 3: Biophysical Techniques in Photosynthesis Wisconsin at Oshkosh, Wisconsin, and J. Kenneth (24 Chapters; 411 pages; 1996; edited by the late Jan Hoober of the Arizona State University, Tempe, Amesz and the late Arnold J. Hoff, from The Arizona. Two of the earlier AIPH volumes have in- Netherlands; ISBN: 0-7923-3642-9); cluded descriptions of plastids: Volume 7 (The Volume 4: Oxygenic Photosynthesis: The Light Molecular Biology of Chloroplasts and Mitochondria Reactions (34 Chapters; 682 pages; 1996; edited by in Chlamydomonas, edited by Jean-David Rochaix, Donald R. Ort and Charles F. Yocum, from USA; Michel Goldschmidt-Clermont and Sabeeha Mer- ISBN: 0-7923-3683-6); chant); and Volume 14 (Photosynthesis in Algae, Volume 5: Photosynthesis and the Environment (20 edited by Anthony Larkum, Susan Douglas, and John Chapters; 491 pages; 1996; edited by Neil R. -
Evolution, Development, and the Units of Selection (Epigenesis/Modern Synthesis/Preformation/Somatic Embryogenesis/Weismann's Doctrine) LEO W
Proc. Nat. Acad. Sci. USA Vol. 80, pp. 1387-1391, March 1983 Evolution Evolution, development, and the units of selection (epigenesis/Modern Synthesis/preformation/somatic embryogenesis/Weismann's doctrine) LEO W. Buss Department of Biology and Peabody Museum of Natural History, Yale University, New Haven, Connecticut 06511 Communicated by G, Evelyn Hutchinson, December 17, 1982 ABSTRACT The "Modern Synthesis" forms the foundation of those working with the comparative embryology of vertebrates, current evolutionary theory. It is based on variation among indi- saw strong evidence for Weismann's scheme in the sequestering viduals within populations. Variations within individuals are be- of germ cells during early embryology. Finally, several inves- lieved to hold no phylogenetic significance because such variation tigators studying wound-healing had clearly illustrated that many cannot be transmitted to the germ line (i.e., Weismann's doctrine). somatic cells were, in fact, incapable of regeneration. Weismann's doctrine, however, does not apply to protists, fungi, Support for Weismann's doctrine was by no means universal. or plants and is an entirely unsupported assumption for 19 phyla Botanists were Weismann's earliest critics (5). Debate over the of animals. This fact requires that the Modern Synthesis be reex- issue was central in the development of the continuing rift be- amined and modified. tween botanists and zoologists despite the commonality of their interests (G. E. Hutchinson, personal communication). Al- The Darwinian notion of evolution as a process directed by se- though Weismann's doctrine was the subject of two very critical lection acting upon heritable variation has not been challenged reviews in the 20th century (6, 7), these criticisms fell on deaf seriously since Darwin first articulated it. -
The Ascent of Water in Plants
Ch19.qxd 8/19/04 6:35 PM Page 315 197 The Ascent of Water in Plants The problem of the rise of water in tall plants is as old as the science of plant physiology. In this chapter we consider the cohesion theory, which is the best formulation to explain how water can get to the top of tall trees and vines. I. THE PROBLEM Let us consider why it is hard for water to get to the top of trees. A suc- tion pump can lift water only to the barometric height, which is the height that is supported by atmospheric pressure (1.0 atm) or 1033 cm (10.33 m; 33.89 feet) (Salisbury and Ross, 1978, p. 49). If a hose or pipe is sealed at one end and filled with water, and then placed in an upright position with the open end down and in water, atmospheric pressure will support the water column to 10.33 meters, theoretically. At this height the pressure equals the vapor pressure of water at its temperature. Above this height of 1033 cm, water turns to vapor. When the pressure is reduced in a column of water so that vapor forms or air bubbles appear (the air coming out of solution), the column is said to cavitate (Salisbury and Ross, 1978, p. 49). My father, Don Kirkham, and his students tried to see how far they could climb the outside back stairs of the Agronomy Building at Iowa State University with a hose, closed end in hand and with the hose’s bottom in a water bucket on the ground. -
Induction of Mitochondrial DNA Heteroplasmy by Intra- and Interspecific Transplantation of Germ Plasm in Drosophila
Copyright 0 1989 by the Genetics Society of America Induction of Mitochondrial DNA Heteroplasmy by Intra- and Interspecific Transplantation of Germ Plasm in Drosophila Etsuko T. Matsuura,* SadaoI. Chigusa* and Yuzo Niki? *Department of Biology, Ochanomiru University, 2-1-1 Otsuka, Bunkyo-ku, Tokyo 112, Japanand tDepartment $Biology, Ibaraki University, 2-1-1 Bunkyo, Mito-shi, Ibaraki 310, Japan Manuscript received January 17, 1989 Accepted for publication April 3, 1989 ABSTRACT A new experimental system for inducing mitochondrial DNA heteroplasmy in Drosophila was developed. By transplanting the germ plasm of Drosophila melanogaster and Drosophila mauritiana into the posterior pole of the recipient eggs of D. melanogaster, it was possible to introduce foreign mitochondria into the recipient female germline. Heteroplasmic individuals containing both donor and recipient mtDNA were obtained in intra- and interspecific combinations at similar frequencies. The proportion of donor-derived mtDNA in the heteroplasmic individuals varied considerably from individual to individual irrespectiveof the donor species used. No significant decreasein or elimination of donor mtDNA was observed, andthe heteroplasmic statein female germlines persisted for several generations. The present system should serve very much to promote the study and clarification of the transmission gkneticsof mtDNA in insects. HE geneticsof metazoan mitochondrial DNA germ plasm. The germline ofDrosophila is segregated T (mtDNA) is unique in that apopulation of fromother somatic lines at very earlyembryonic mtDNA molecules is maternallyinherited. Lack of stages through thefunction of germ plasm (ILLMENSEE appropriate genetic markers of mitochondria within and MAHOWALD1974; NIKI 1986). Germ plasm is not an individual makes difficult elucidation of the man- species-specific for inducingfunctional germ cells ner in which mitochondria or mtDNA are transmit- (MAHOWALD,ILLMENSEE and TURNER1976) andcon- ted.