(Occurs Inside Sperm Tube) Mitosis Spermatogoni
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Evolution of Oviductal Gestation in Amphibians MARVALEE H
THE JOURNAL OF EXPERIMENTAL ZOOLOGY 266394-413 (1993) Evolution of Oviductal Gestation in Amphibians MARVALEE H. WAKE Department of Integrative Biology and Museum of Vertebrate Zoology, University of California,Berkeley, California 94720 ABSTRACT Oviductal retention of developing embryos, with provision for maternal nutrition after yolk is exhausted (viviparity) and maintenance through metamorphosis, has evolved indepen- dently in each of the three living orders of amphibians, the Anura (frogs and toads), the Urodela (salamanders and newts), and the Gymnophiona (caecilians). In anurans and urodeles obligate vivi- parity is very rare (less than 1%of species); a few additional species retain the developing young, but nutrition is yolk-dependent (ovoviviparity) and, at least in salamanders, the young may be born be- fore metamorphosis is complete. However, in caecilians probably the majority of the approximately 170 species are viviparous, and none are ovoviviparous. All of the amphibians that retain their young oviductally practice internal fertilization; the mechanism is cloaca1 apposition in frogs, spermato- phore reception in salamanders, and intromission in caecilians. Internal fertilization is a necessary but not sufficient exaptation (sensu Gould and Vrba: Paleobiology 8:4-15, ’82) for viviparity. The sala- manders and all but one of the frogs that are oviductal developers live at high altitudes and are subject to rigorous climatic variables; hence, it has been suggested that cold might be a “selection pressure” for the evolution of egg retention. However, one frog and all the live-bearing caecilians are tropical low to middle elevation inhabitants, so factors other than cold are implicated in the evolu- tion of live-bearing. -
Identifying Lethal Temperatures Targeting Immature Life Stage Control of Spotted Wing Drosophila
AGRICULTURAL RESEARCH FOUNDATION FINAL REPORT FUNDING CYCLE 2015 – 2017 TITLE: Identifying Lethal Temperatures Targeting Immature Life Stage Control of Spotted Wing Drosophila RESEARCH LEADER: Vaughn Walton COOPERATORS: Daniel Dalton, Riki York SUMMARY: Survival of spotted wing drosophila (D. suzukii, SWD) larvae to adulthood was evaluated after exposure to temperatures ranging 29-49°C in a laboratory thermal gradient bench for 60 minutes. Vials filled with pre-made fly diet up to approximately 1.5 cm from the bottom were used as oviposition media inside the gradient wells. Forty-three vials were prepared each day for 4 consecutive days. Five adult females were placed in each of 36 vials for 24 hours for oviposition to occur, seven vials were held as controls without flies. Upon removal, adult flies were placed in ethanol. Four ages were tested between 1-4-day old egg/larvae (i.e. 1 day old, 2 days old, 3 days old, and four days old). Sample vials were examined for oviposition success. Immature flies exposed temperatures of 32-35°C had the highest survival to adulthood. Above 38°C survival to adulthood with no survival at 41°C and 49°C, and a few surviving to adulthood under 45°C. An additional trial was conducted to evaluate the potential for thermal conditioning to improve larval survival at higher temperatures. For this study, four-day-old larvae were subject to 30, 60, and 90 minutes at 35°C, then allowed to cool to room temperature (22°C) for 60 minutes prior to placement in the thermal bench. These trials were used to determine how heat may reduce successful development to adulthood, leading to better management practices in the field. -
The Reproductive Biology of Pempheris Schwenkii (Pempheridae)
Zoological Studies 51(7): 1086-1093 (2012) The Reproductive Biology of Pempheris schwenkii (Pempheridae) on Okinawa Island, Southwestern Japan Keita Koeda1,*, Taiki Ishihara1, and Katsunori Tachihara2 1Graduate School of Engineering and Science, University of the Ryukyus, 1 Senbaru, Nishihara, Okinawa 903-0213, Japan 2Faculty of Science, University of the Ryukyus, 1 Senbaru, Nishihara, Okinawa 903-0213, Japan. E-mail:[email protected] (Accepted May 24, 2012) Keita Koeda, Taiki Ishihara, and Katsunori Tachihara (2012) The reproductive biology of Pempheris schwenkii (Pempheridae) on Okinawa Island, southwestern Japan. Zoological Studies 51(7): 1086-1093. The reproductive biology of Pempheris schwenkii, one of the most common nocturnal fishes in Okinawan waters, was studied using a total of 1834 specimens (3.1-125.9 mm standard length, SL) collected around Okinawa I. The spawning season was estimated to occur from Jan. to June, with a peak from Feb. to May, based on monthly changes in the gonadosomatic index and histological observations of the ovaries. The relationship between the SL and the appearance of mature females, and the monthly growth of the 0+ group suggested that maturity occurred at ca. 70 mm SL, corresponding to 1 yr after hatching. Spawning was not related to the lunar cycle. The batch fecundity of P. schwenkii was calculated as ca. 700-4100 eggs. Pempheris schwenkii appeared to spawn at night based on diurnal changes in the frequency of females exhibiting hydrated ovaries and postovulatory follicles. Such nighttime spawning seems to reduce the risk of predation of adults and eggs, which may be an adaptive characteristic of nocturnal fishes. -
Fundamentals of Fisheries Biology
FT 273 - FUNDAMENTALS OF FISHERIES BIOLOGY 9 March 2015 Reproduction TOPICS WE WILL COVER REGARDING REPRODUCTION Reproductive anatomy Breeding behavior Development Physiological adaptations Bioenergetics Mating systems Alternative reproductive strategies Sex change REPRODUCTION OVERVIEW Reproduction is a defining feature of a species and it is evident in anatomical, behavioral, physiological and energetic adaptations Success of a species depends on ability of fish to be able to reproduce in an ever changing environment REPRODUCTION TERMS Fecundity – Number of eggs in the ovaries of the female. This is most common measure to reproductive potential. Dimorphism – differences in size or body shape between males and females Dichromatism – differences in color between males and females Bioenergetics – the balance of energy between growth, reproduction and metabolism REPRODUCTIVE ANATOMY Different between sexes Different depending on the age/ size of the fish May only be able to determine by internal examination Reproductive tissues are commonly paired structures closely assoc with kidneys FEMALE OVARIES (30 TO 70%) MALE TESTES (12% OR <) Anatomy hagfish, lamprey: single gonads no ducts; release gametes into body cavity sharks: paired gonads internal fertilization sperm emitted through cloaca, along grooves in claspers chimaeras, bony fishes: paired gonads external and internal fertilization sperm released through separate opening most teleosts: ova maintained in continuous sac from ovary to oviduct exceptions: Salmonidae, Anguillidae, Galaxidae, -
The Function and Evolution of Egg Colour in Birds
University of Windsor Scholarship at UWindsor Electronic Theses and Dissertations Theses, Dissertations, and Major Papers 2012 The function and evolution of egg colour in birds Daniel Hanley University of Windsor Follow this and additional works at: https://scholar.uwindsor.ca/etd Recommended Citation Hanley, Daniel, "The function and evolution of egg colour in birds" (2012). Electronic Theses and Dissertations. 382. https://scholar.uwindsor.ca/etd/382 This online database contains the full-text of PhD dissertations and Masters’ theses of University of Windsor students from 1954 forward. These documents are made available for personal study and research purposes only, in accordance with the Canadian Copyright Act and the Creative Commons license—CC BY-NC-ND (Attribution, Non-Commercial, No Derivative Works). Under this license, works must always be attributed to the copyright holder (original author), cannot be used for any commercial purposes, and may not be altered. Any other use would require the permission of the copyright holder. Students may inquire about withdrawing their dissertation and/or thesis from this database. For additional inquiries, please contact the repository administrator via email ([email protected]) or by telephone at 519-253-3000ext. 3208. THE FUNCTION AND EVOLUTION OF EGG COLOURATION IN BIRDS by Daniel Hanley A Dissertation Submitted to the Faculty of Graduate Studies through Biological Sciences in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy at the University of Windsor Windsor, Ontario, Canada 2011 © Daniel Hanley THE FUNCTION AND EVOLUTION OF EGG COLOURATION IN BIRDS by Daniel Hanley APPROVED BY: __________________________________________________ Dr. D. Lahti, External Examiner Queens College __________________________________________________ Dr. -
Fishery Science – Biology & Ecology
Fishery Science – Biology & Ecology How Fish Reproduce Illustration of a generic fish life cycle. Source: Zebrafish Information Server, University of South Carolina (http://zebra.sc.edu/smell/nitin/nitin.html) Reproduction is an essential component of life, and there are a diverse number of reproductive strategies in fishes throughout the world. In marine fishes, there are three basic reproductive strategies that can be used to classify fish. The most common reproductive strategy in marine ecosystems is oviparity. Approximately 90% of bony and 43% of cartilaginous fish are oviparous (See Types of Fish). In oviparous fish, females spawn eggs into the water column, which are then fertilized by males. For most oviparous fish, the eggs take less energy to produce so the females release large quantities of eggs. For example, a female Ocean Sunfish is able to produce 300 million eggs over a spawning cycle. The eggs that become fertilized in oviparous fish may spend long periods of time in the water column as larvae before settling out as juveniles. An advantage of oviparity is the number of eggs produced, because it is likely some of the offspring will survive. However, the offspring are at a disadvantage because they must go through a larval stage in which their location is directed by oceans currents. During the larval stage, the larvae act as primary consumers (See How Fish Eat) in the food web where they must not only obtain food but also avoid predation. Another disadvantage is that the larvae might not find suitable habitat when they settle out of the ~ Voices of the Bay ~ [email protected] ~ http://sanctuaries.noaa.gov/education/voicesofthebay.html ~ (Nov 2011) Fishery Science – Biology & Ecology water column. -
Comparative Biology of Oogenesis in Nemertean Worms Stephen A
AaaZoologka (Stockholm) 82: 213-230 (July 2001) Comparative biology of oogenesis in nemertean worms Stephen A. Strieker1, Toni L. Smythe1, Leonard Miller1 and Jon L. Norenburg2 Abstract 'Department of Biology, University of New Strieker, S. A., Smythe,T, L., Miller, L. and Norenburg, J. L. 2001. Mexico, Albuquerque, NM 87131; Comparative biology of oogenesis in nemertean worms. — Acta Zoobgica 2 Invertebrate Zoology, MRC 163,Museum (Stockholm) 82: 213-230 of Natural History, Washington, DC 20560 USA In order to supplement previous analyses of oogenesis in nemertean worms, this study uses light and electron microscopy to compare the ovaries and Keywords: oocytes in 16 species of nemerteans that represent various taxa within the ovary, ultrastructure, vitellogenesis, yolk, phylum, Nemertean ovaries comprise serially repeated sacs with an ovarian nucleoli, endoplasmic reticulum, confocal wall that characteristically includes myofilament-containing cells interspersed microscopy, oocyte maturation, serotonin among the germinal epithelium. Each oocyte can attach to the germinal epithelium by a vegetally situated stalk and resides in the ovarian lumen Accepted for publication: without being surrounded by follicle cells. In the ovary, oocytes arrest at 26 September 2000 prophase I of meiosis and contain a hypertrophied nucleus ('germinal vesicle') that often possesses multiple nucleoli. Intraovarian growth apparently involves an autosynthetic mode of yolk formation in most nemerteans and generates oocytes that measure ~60 Jim to 1 mm. When fully developed, oocytes can be discharged through a short gonoduct and are either spawned freely or deposited within egg cases. In most species, oocytes released from the ovary possess extracellular coats and resume maturation by undergoing germinal vesicle breakdown (GVBD). -
Discovery of a New Mode of Oviparous Reproduction in Sharks and Its Evolutionary Implications Kazuhiro Nakaya1, William T
www.nature.com/scientificreports OPEN Discovery of a new mode of oviparous reproduction in sharks and its evolutionary implications Kazuhiro Nakaya1, William T. White2 & Hsuan‑Ching Ho3,4* Two modes of oviparity are known in cartilaginous fshes, (1) single oviparity where one egg case is retained in an oviduct for a short period and then deposited, quickly followed by another egg case, and (2) multiple oviparity where multiple egg cases are retained in an oviduct for a substantial period and deposited later when the embryo has developed to a large size in each case. Sarawak swellshark Cephaloscyllium sarawakensis of the family Scyliorhinidae from the South China Sea performs a new mode of oviparity, which is named “sustained single oviparity”, characterized by a lengthy retention of a single egg case in an oviduct until the embryo attains a sizable length. The resulting fecundity of the Sarawak swellshark within a season is quite low, but this disadvantage is balanced by smaller body, larger neonates and quicker maturation. The Sarawak swellshark is further uniquely characterized by having glassy transparent egg cases, and this is correlated with a vivid polka‑dot pattern of the embryos. Five modes of lecithotrophic (yolk-dependent) reproduction, i.e. short single oviparity, sustained single oviparity, multiple oviparity, yolk‑sac viviparity of single pregnancy and yolk‑sac viviparity of multiple pregnancy were discussed from an evolutionary point of view. Te reproductive strategies of the Chondrichthyes (cartilaginous fshes) are far more diverse than those of the other animal groups. Reproduction in chondrichthyan fshes is divided into two main modes, oviparity (egg laying) and viviparity (live bearing). -
Viviparity in a Triassic Marine Archosauromorph Reptile.Pdf
第55卷 第3期 古 脊 椎 动 物 学 报 pp. 210-217 2017年7月 VERTEBRATA PALASIATICA fig. 1 Viviparity in a Triassic marine archosauromorph reptile LI Chun1 Olivier RIEPPEL2 Nicholas C. FRASER3 (1 Key Laboratory of Vertebrate Evolution and Human Origins of Chinese Academy of Sciences, Institute of Vertebrate Palaeontology and Palaeoanthropology, Chinese Academy of Sciences Beijing 100044, China [email protected]) (2 Field Museum of Natural History Chicago IL 60605, USA) (3 National Museums Scotland Edinburgh EH1 1JF, UK) Abstract Eggs or embryos have been reported in various groups of fossil reptiles, where viviparity is a common mode of reproduction in aquatic taxa such as the ichthyopterygians, some groups of sauropterygians, mosasauroids, some taxa of choristoderans and certain protorosaurs. Here, we describe a complete embryo of a marine protorosaur, based on a well-preserved, curled- up skeleton. The new discovery is referred to a taxon closely related to the remarkable long- necked Dinocephalosaurus. It further confirmed viviparity in an archosauromorph group and indicates an increasing taxonomic diversity not only within this group, but of Triassic marine reptiles in general. keywords archosauromorph, protorosaur, embryo, viviparity, marine Citation Li C, Rieppel O, Fraser N C, 2017. Viviparity in a Triassic marine archosauromorph reptile. Vertebrata PalAsiatica, 55(3): 210–217 1 Introduction A number of terms such as oviparity, ovoviviparity and viviparity have been used to describe reproductive strategies in reptiles. However, in the fossil record only oviparity and viviparity can be distinguished, thus allowing a straight-forward definition simply based on the deposition of eggs versus giving birth to live offspring (Guillette, 1993; Blackburn, 1993). -
Zootoca Vivipara, Lacertidae) and the Evolution of Parity
Blackwell Science, LtdOxford, UKBIJBiological Journal of the Linnean Society0024-4066The Linnean Society of London, 2004? 2004 871 111 Original Article EVOLUTION OF VIVIPARITY IN THE COMMON LIZARD Y. SURGET-GROBA ET AL. Biological Journal of the Linnean Society, 2006, 87, 1–11. With 4 figures Multiple origins of viviparity, or reversal from viviparity to oviparity? The European common lizard (Zootoca vivipara, Lacertidae) and the evolution of parity YANN SURGET-GROBA1*, BENOIT HEULIN2, CLAUDE-PIERRE GUILLAUME3, MIKLOS PUKY4, DMITRY SEMENOV5, VALENTINA ORLOVA6, LARISSA KUPRIYANOVA7, IOAN GHIRA8 and BENEDIK SMAJDA9 1CNRS UMR 6553, Laboratoire de Parasitologie Pharmaceutique, 2, Avenue du Professeur Léon Bernard, 35043 Rennes Cedex, France 2CNRS UMR 6553, Station Biologique de Paimpont, 35380 Paimpont, France 3EPHE, Ecologie et Biogéographie des Vertébrés, 35095 Montpellier, France 4Hungarian Danube Research Station of the Institute of Ecology and Botany of the Hungarian Academy of Sciences, 2131 God Javorka S. u. 14., Hungary 5Severtsov Institute of Ecology and Evolution, Russian Academy of Sciences,33 Leninskiy Prospect, 117071 Moscow, Russia 6Zoological Museum of the Moscow State University, Bolshaja Nikitskaja 6, 103009 Moscow, Russia 7Zoological Institute, Russian Academy of Sciences, Universiteskaya emb. 1, 119034 St Petersburg, Russia 8Department of Zoology, Babes-Bolyai University, Str. Kogalniceanu Nr.1, 3400 Cluj-Napoca, Romania 9Institute of Biological and Ecological Sciences, Faculty of Sciences, Safarik University, Moyzesova 11, SK-04167 Kosice, Slovak Republic Received 23 January 2004; accepted for publication 1 January 2005 The evolution of viviparity in squamates has been the focus of much scientific attention in previous years. In par- ticular, the possibility of the transition from viviparity back to oviparity has been the subject of a vigorous debate. -
Fish Reproductive Biology
OHIO AGRICULTURAL RESEARCH AND DEVELOPMENT CENTER Fish Reproductive Biology OSU South Centers Piketon, Ohio [email protected] OHIO AGRICULTURAL RESEARCH AND DEVELOPMENT CENTER Fish Facts • 32,500 estimated species of fish in the world • More than 15,000 freshwater fish species • Freshwater may constitute less than 0.3% of available global water 2 OHIO AGRICULTURAL RESEARCH AND DEVELOPMENT CENTER 3 OHIO AGRICULTURAL RESEARCH AND DEVELOPMENT CENTER Types of Reproduction • SEXUAL REPRODUCTION • Combination of genetic material contributed by two different gametes, usually i.e. two different individuals, male and female • ASEXUAL (PARTHENOGENESIS) • New individuals are produced from a single parent without the formation of gametes or need of a partner (Amazon Molly) 4 OHIO AGRICULTURAL RESEARCH AND DEVELOPMENT CENTER Sexual Maturity • Fishes can become sexually mature at various ages, depending on species • Several factors influence sexual maturity • Nutritional state of the fish • Physiological factors (hormones) • Ecological factors 5 OHIO AGRICULTURAL RESEARCH AND DEVELOPMENT CENTER Sexual Maturity • Most bony fishes become sexually mature between one and five years • Sturgeon may take up to 15 years • Most bony fishes are in excess of 8 cm (3 in.) before reproducing • Age and associated size are major factors • Species of small size begin reproduction sooner than species of large size 6 OHIO AGRICULTURAL RESEARCH AND DEVELOPMENT CENTER Sexual Dimorphism • In most species of fish the females are larger than the males(sexual dimorphism) -
Evolution of the Animal Phyla Chapter 19 General Features of Animals • All Animals Are Multicellular Heterotrophs
Evolution of the Animal Phyla Chapter 19 General Features of Animals • All animals are multicellular heterotrophs. • Invertebrates account for 99% of all species. • Animal Kingdom includes about 36 phyla. Most occur in the sea. Three phyla dominate animal life on land. - Arthropoda (spiders and insects) - Mollusca (snails) - Chordata (vertebrates) Phylogeny of Kingdom Animalia Key development genes are ancient: Homeotic genes Direct embryological development - Produce groups of proteins that turn genes on and off during development Found in every eukaryote analyzed so far; yeasts, plants, earthworms, frogs, chickens, mice and humans Trends in the evolution of animals • Reproduction Asexual – mitosis - Reproduction by fission or budding - Parthenogenesis Sexual – meiosis - Reproduction- external fertilization to internal - Embryo development external to internal ¾ Oviparous ¾ Ovoviviparous ¾ Viviparous Evolution of Nervous System Sponges • Kingdom Animalia has two subkingdoms: Parazoa - lack definite symmetry and tissues organized into organs. - Dominated by sponges (Porifera). Eumetazoa - have definite shape and and symmetry and highly specialized cells. • Sponges are simplest animals. Bodies consist of masses of specialized cells embedded in gel-like matrix. Phylum Porifera Cellular level of organization with no tissues or organs 1. The only major animal group phyla to lack nerve cells 2. External fertilization no specialized gametes (male and female gametes appear similar Asexual and sexual reproduction Key evolutionary advance: symmetry and tissues. (~3000 species); 1. Have no head, no centralized nervous system (only a nerve net), 2. Exhibit alternation of asexual polypoid and sexual medusoid generations. Fertilization and development is external to the body Phylum Cnidaria corals, sea anemones, jelly fish, hydra etc. Key evolutionary advance: symmetry and tissues.