Egg-Laying Intervals in Shorebirds

Total Page:16

File Type:pdf, Size:1020Kb

Egg-Laying Intervals in Shorebirds 50 Wader Study Group Bulletin Egg-laying intervals in shorebirds MARK A. COLWELL Wildlife Department, Humboldt State University, Arcata, CA 95521 USA. [email protected] Colwell, M.A. 2006. Egg-laying intervals in shorebirds. Wader Study Group Bull. 111: 50–59. Keywords: Shorebird, wader, egg laying interval, breeding phenology. The interval between consecutive eggs laid in a clutch by female birds is highly variable, ranging from one day to several weeks. I summarize data for 71 species of shorebird and examine relationships between mini- mum egg-laying intervals and constraints imposed by: 1) time, represented by breeding latitude and length of breeding season; 2) energy, as gauged by relationship between egg mass and female mass; and 3) risk of losing a clutch, measured by whether a species conceals eggs in a nest amidst vegetation or nests in the open. Among shorebirds, the interval is either one (e.g., most sandpipers) or two days (principally plovers, thick-knees and oystercatchers). There was no evidence that longer intervals correlate with greater female investment in egg (or clutch) mass. However, species breeding in more northerly latitudes (with shorter breeding seasons) are more likely to lay at daily intervals than species occupying temperate or tropical environs. A greater percent- age of species that nest in vegetation that conceal eggs and incubating adults laid eggs at daily intervals compared with species nesting in open habitats. These latter two relationships are, however, confounded by taxonomy because sandpipers, which have a northerly breeding distribution and conceal nests, differ from plovers, thick-knees and oystercatchers, which principally breed in open habitats of temperate and tropical latitudes. Nevertheless, it is plausible that in addition to long breeding seasons, longer laying intervals in open- nesting species have evolved as a response to frequent clutch loss owing to predators or the environment. INTRODUCTION (Carey 1996, Lack 1968). Interestingly, egg-laying intervals for these taxa are never as short as 24 h. Consequently, it Among vertebrates, birds are the most uniform in reproduc- appears that virtually all birds can be categorized into one of tive biology: all species are oviparous. Despite this uniform- two groups based on the shortest (hereafter minimum) laying ity, remarkable variation exists across taxa and among interval, species that: 1) regularly lay at intervals of one day, individuals within species in various facets of oviparity or 2) rarely or never lay at intervals of one day. It is true, (Carey 1996). A relatively unexplored facet of egg-laying is however, that within both groups energy (or nutrient) short- the interval between successive eggs in a clutch. The rate at ages can lengthen egg laying beyond this minimum interval which females lay consecutive eggs varies among species, (Carey 1996, Lack 1968). and tends to be slower in larger taxa (Lack 1968, Winkler Variation in egg-laying intervals among and within species 2004) and those with smaller clutches (Johnson 2000, Lack may be related to three principal ecological factors (Carey 1968). Although egg-laying intervals are well known in 1996, Lack 1968): 1) time constraints associated with length commercially exploited taxa, they remain relatively poorly of breeding season, 2) energy costs of forming eggs, and 3) understood in wild birds, probably owing to the difficulty of risk of clutch loss to predators. Species that breed at high recording precisely the timing of oviposition (Shubert 1990). latitudes (or elevations) lay eggs quicker owing to the need In the domestic chicken Gallus domesticus, a single func- to complete breeding in a shorter season, compared to taxa tional left ovary ovulates at approximately 24-h intervals and at southerly latitudes (Morton 1976). The availability of food oviposition occurs at slightly greater than this interval (energy) or nutrients (e.g. calcium) serve as proximate con- (Johnson 2000). However, even in the chicken, where a trols of egg laying, as evidenced by experimentally length- sequence (synonymous with clutch) may vary from 2–9 eggs, ened intervals in female Mallards Anas platyrhynchos denied the rate of egg production (laying) ranges from 25–28.5 h, food during the period of rapid follicular growth (Johnson and this correlates negatively with number of eggs laid 2000). And, in wild species that rely on exogenous energy (Johnson 2000). sources to form eggs, egg-laying intervals commonly exceed For wild birds, even those taxa with two functional ovi- the minimum during periods of inclement weather (Carey ducts (e.g. some Falconiformes, Apterygiformes), females 1996, Lack 1968, Wiebe & Martin 1995). Food also may be never lay eggs at shorter than 24 h intervals (Winkler 2004). an ultimate factor, interacting with mode of development Many species lay eggs daily, including most passerines, (precocial vs altricial) to shape egg-laying intervals. Species waterfowl, and many shorebirds (Lack 1968). By contrast, that lay disproportionately large eggs (relative to female body other species lay consecutive eggs at periods exceeding 24 h, size; e.g., megapodes, penguins) lay at longer intervals. Lack ranging upwards from 2–3 days (e.g., plovers, seabirds), and (1968), however, noted that among seabirds, which lay 4–8 days (e.g., megapodes, penguins) to 14–30 days (kiwis) disproportionately small eggs relative to female body size, Bulletin 111 December 2006 50 Colwell: Egg-laying intervals in shorebirds 51 egg-laying intervals are long (2–5 days); he suggested that as nesting in one of two categories (open vs concealed) based this was evidence for food limitation at the time of egg lay- on a composite of habitat features and the behavioural ing. Lastly, predation may shape egg-laying intervals via the response of adults to danger posed by potential nest preda- risk of losing a clutch of eggs during the laying process (Lack tors (Gochfeld 1984). Briefly, open-nesting species (e.g., 1968). This reasoning, however, addresses the energetics of plovers, avocets and stilts, oystercatchers, and thick-knees) replacing failed clutches rather than danger to a laying are those that did not use vegetation to conceal eggs in the female. nest or incubating adults. In the presence of potential egg Here, I examine variation in minimum egg-laying intervals predators, incubating adults typically slip off the nest quietly in shorebirds in relation to time, energy and risk of clutch and rely on egg crypsis to evade predators; some species mob failure. Shorebirds are an intriguing group in which to study predators. By contrast, concealed nesters (e.g., sandpipers) egg-laying intervals because they: 1) are diverse and well- are those that nest in vegetation that hides cryptically- studied; 2) breed from the high arctic to tropical latitudes; 3) plumaged adults and eggs. Concealed nesters typically react mostly rely on exogenous food resources (see Lenington at closer distances to the approach of a predator by perform- 1984) to lay small clutches; 4) often experience high, but ing distraction displays (e.g. “mouse run”; Gochfeld 1984). variable, rates of clutch failure (Evans & Pienkowski 1984); Specifically, I predicted that species occupying open habitats and 5) either conceal their clutches in vegetation (e.g., sand- (where clutches are at greater risk of loss) would have longer pipers) or nest in open habitats (e.g., plovers, avocets, thick- laying intervals than taxa nesting in vegetated habitats. I used knees), which correlates with the behaviour of adults disturbed chi-square tests to compare the frequencies of species in dif- from incubation (Gochfeld 1984). ferent categories. METHODS RESULTS I reviewed species accounts (in, for example, Birds of North Summary of egg-laying intervals America, Birds of the Western Palearctic, The Birds of Africa) and original scientific literature summarizing details Nearly all shorebirds could be categorized into one of two on breeding biology to compile information (Appendix) on categories. The first group, primarily sandpipers (40), avocets the following variables. I summarized egg-laying intervals to (4), some plovers (11), and an oystercatcher, consisted of 55 the nearest hour when available. However, owing to the dif- species in which females regularly laid eggs at daily intervals. ficulty in accurately determining egg-laying intervals A second group, comprised of thick-knees (2), plovers (12) (Shubert 1990), many authors described the time between and oystercatchers (2), included 16 species in which females successive eggs in a clutch based on daily intervals. So, I rarely or never laid a clutch at intervals shorter than two days; categorized the interval between successive eggs as daily or for most of these species, the egg-laying intervals often longer. Clutch size was the modal number of eggs laid by a exceeded 2 days. For both groups, however, egg-laying female. Fresh mass (g) of eggs and females came from spe- intervals occasionally exceeded the minimum, especially cies accounts or Dunning (1993). during periods of food shortage or inclement weather. For To evaluate time constraints, I compared the frequency example, Nethersole-Thompson & Nethersole-Thompson with which species laid at one day or longer intervals across (1979) recorded precisely Greenshank laying intervals (h) at four latitudinal categories (tropical, temperate, boreal and 26 nests and noted that the usual 2-day (c.44 hour) interval arctic) corresponding to decreasing length of the breeding often lengthened during cool, wet weather. This was true for season. Specifically, if time constrained laying, then a greater other species that laid at longer intervals. For example, the percentage of northerly taxa should have daily egg-laying time between consecutive eggs laid by female Snowy (Kent- intervals compared to those breeding at temperate or tropi- ish) Plovers often lengthened from 2 to 3–5 days during cal latitudes. As another measure of time constraints, I char- periods of cool, wet weather of March and April in coastal acterized length of breeding season (number of weeks) over northern California (Page et al.
Recommended publications
  • BIO 313 ANIMAL ECOLOGY Corrected
    NATIONAL OPEN UNIVERSITY OF NIGERIA SCHOOL OF SCIENCE AND TECHNOLOGY COURSE CODE: BIO 314 COURSE TITLE: ANIMAL ECOLOGY 1 BIO 314: ANIMAL ECOLOGY Team Writers: Dr O.A. Olajuyigbe Department of Biology Adeyemi Colledge of Education, P.M.B. 520, Ondo, Ondo State Nigeria. Miss F.C. Olakolu Nigerian Institute for Oceanography and Marine Research, No 3 Wilmot Point Road, Bar-beach Bus-stop, Victoria Island, Lagos, Nigeria. Mrs H.O. Omogoriola Nigerian Institute for Oceanography and Marine Research, No 3 Wilmot Point Road, Bar-beach Bus-stop, Victoria Island, Lagos, Nigeria. EDITOR: Mrs Ajetomobi School of Agricultural Sciences Lagos State Polytechnic Ikorodu, Lagos 2 BIO 313 COURSE GUIDE Introduction Animal Ecology (313) is a first semester course. It is a two credit unit elective course which all students offering Bachelor of Science (BSc) in Biology can take. Animal ecology is an important area of study for scientists. It is the study of animals and how they related to each other as well as their environment. It can also be defined as the scientific study of interactions that determine the distribution and abundance of organisms. Since this is a course in animal ecology, we will focus on animals, which we will define fairly generally as organisms that can move around during some stages of their life and that must feed on other organisms or their products. There are various forms of animal ecology. This includes: • Behavioral ecology, the study of the behavior of the animals with relation to their environment and others • Population ecology, the study of the effects on the population of these animals • Marine ecology is the scientific study of marine-life habitat, populations, and interactions among organisms and the surrounding environment including their abiotic (non-living physical and chemical factors that affect the ability of organisms to survive and reproduce) and biotic factors (living things or the materials that directly or indirectly affect an organism in its environment).
    [Show full text]
  • Species and Sex Divergence in Vocalizations Between Hybridizing Role-Reversed Shorebirds, Northern Jacana
    bioRxiv preprint doi: https://doi.org/10.1101/757336; this version posted September 6, 2019. 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-NC-ND 4.0 International license. 1 Species and sex divergence in vocalizations between hybridizing role-reversed 2 shorebirds, Northern Jacana (Jacana spinosa) and Wattled Jacana (Jacana 3 jacana) 4 5 Evan J. Buck1, Toni Brown2, Gina Zwicky2, Elizabeth P. Derryberry1,2, Sara E. Lipshutz1,2,3* 6 1Department of Ecology and Evolutionary Biology, University of Tennessee, Knoxville, TN, 7 USA 8 2Department of Ecology and Evolutionary Biology, Tulane University, New Orleans, LA, USA 9 3Department of Biology, Indiana University, Bloomington, IN, USA 10 * Corresponding author: [email protected] 11 12 ABSTRACT—Species-specific vocalizations can act as a reproductive isolating mechanism 13 between closely related populations. We analyzed vocal divergence between two hybridizing 14 species of sex-role reversed polyandrous shorebirds, the Northern Jacana (Jacana 15 spinosa) and Wattled Jacana (Jacana jacana). We found that J. spinosa calls have higher peak 16 frequency and fundamental frequency than J. jacana calls. We also compared calls 17 between males and females, as both jacana species are sex-role reversed and females compete for 18 male mates. Males produce calls with a higher peak frequency, exhibit shorter note lengths and 19 emit a greater number of notes within a calling bout than females, which could relate to mate 20 attraction. These results suggest that vocal divergence could act as a behavioral barrier to limit 21 hybridization between the species and vocalizations may function differently between male and 22 female jacanas.
    [Show full text]
  • Wildlife Ecology Provincial Resources
    MANITOBA ENVIROTHON WILDLIFE ECOLOGY PROVINCIAL RESOURCES !1 ACKNOWLEDGEMENTS We would like to thank: Olwyn Friesen (PhD Ecology) for compiling, writing, and editing this document. Subject Experts and Editors: Barbara Fuller (Project Editor, Chair of Test Writing and Education Committee) Lindsey Andronak (Soils, Research Technician, Agriculture and Agri-Food Canada) Jennifer Corvino (Wildlife Ecology, Senior Park Interpreter, Spruce Woods Provincial Park) Cary Hamel (Plant Ecology, Director of Conservation, Nature Conservancy Canada) Lee Hrenchuk (Aquatic Ecology, Biologist, IISD Experimental Lakes Area) Justin Reid (Integrated Watershed Management, Manager, La Salle Redboine Conservation District) Jacqueline Monteith (Climate Change in the North, Science Consultant, Frontier School Division) SPONSORS !2 Introduction to wildlife ...................................................................................7 Ecology ....................................................................................................................7 Habitat ...................................................................................................................................8 Carrying capacity.................................................................................................................... 9 Population dynamics ..............................................................................................................10 Basic groups of wildlife ................................................................................11
    [Show full text]
  • Biology 2 Lab Packet for Practical 4 Birds
    Bio 2 – Lab Practicum 4 1 Biology 2 Lab Packet For Practical 4 Birds Bio 2 – Lab Practicum 4 2 CLASSIFICATION: Domain: Eukarya Kingdom: Animalia Phylum: Chordata – Chordates Class: Aves – Birds Order: Struthioniformes - Ostriches Order: Galliformes - Quail Order: Rheiformes – Rheas Order: Gruiformes – Coots Order: Casuariiformes – Cassowaries Order: Charadriiformes – Gulls and Allies Order: Apterygiformes – Kiwis Order: Columbiformes – Pigeons Order: Sphenisciformes - Penguins Order: Psittaciformes – Parrots Order: Gaviiformes - Loons Order: Cuculiformes – Roadrunners Order: Podicipediformes – Grebes Order: Strigiformes - Owls Order: Procellariiformes – Tube noses Order: Caprimulgiformes – Nighthawks Order: Pelicaniformes – Pelicans Order: Apodiformes – Hummingbirds Order: Ciconiiformes – Herons/Egrets Order: Trogonifomes – Trogons Order: Phoenicopteriformes - Flamingos Order: Coraciformes – Kingfishers Order: Anseriformes – Ducks Order: Piciformes – Woodpeckers Order: Falconiformes – Raptors Order: Passeriformes - Songbirds Introduction – Birds Although chordates vary widely in appearance, they are distinguished as a phylum by the presence of four anatomical features that appear sometime during their life time. They exhibit deuterostome development and bilateral symmetry. Chordates only comprise 5% of the animal species but may be the most commonly known phylum. Birds are endothermic homeotherms which have adapted to many different ecosystems in the world. Station 1 – Class: Aves 1. What three adaptations do birds have for flight? 2. What do all species of birds have? 3. What dinosaurs did birds emerge within? When did they show up? 4. Where are birds found? Bio 2 – Lab Practicum 4 3 Station 2 – Evolutionary History - Archaeopteryx 1. What characteristics are seen in Archaeopteryx that are bird-like? 2. What characteristics are seen in Archaeopteryx that are reptile-like? Station 3 – General Characteristics - Feathers 1. What are feathers made of? 2.
    [Show full text]
  • 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,
    [Show full text]
  • SHOREBIRDS (Charadriiformes*) CARE MANUAL *Does Not Include Alcidae
    SHOREBIRDS (Charadriiformes*) CARE MANUAL *Does not include Alcidae CREATED BY AZA CHARADRIIFORMES TAXON ADVISORY GROUP IN ASSOCIATION WITH AZA ANIMAL WELFARE COMMITTEE Shorebirds (Charadriiformes) Care Manual Shorebirds (Charadriiformes) Care Manual Published by the Association of Zoos and Aquariums in association with the AZA Animal Welfare Committee Formal Citation: AZA Charadriiformes Taxon Advisory Group. (2014). Shorebirds (Charadriiformes) Care Manual. Silver Spring, MD: Association of Zoos and Aquariums. Original Completion Date: October 2013 Authors and Significant Contributors: Aimee Greenebaum: AZA Charadriiformes TAG Vice Chair, Monterey Bay Aquarium, USA Alex Waier: Milwaukee County Zoo, USA Carol Hendrickson: Birmingham Zoo, USA Cindy Pinger: AZA Charadriiformes TAG Chair, Birmingham Zoo, USA CJ McCarty: Oregon Coast Aquarium, USA Heidi Cline: Alaska SeaLife Center, USA Jamie Ries: Central Park Zoo, USA Joe Barkowski: Sedgwick County Zoo, USA Kim Wanders: Monterey Bay Aquarium, USA Mary Carlson: Charadriiformes Program Advisor, Seattle Aquarium, USA Sara Perry: Seattle Aquarium, USA Sara Crook-Martin: Buttonwood Park Zoo, USA Shana R. Lavin, Ph.D.,Wildlife Nutrition Fellow University of Florida, Dept. of Animal Sciences , Walt Disney World Animal Programs Dr. Stephanie McCain: AZA Charadriiformes TAG Veterinarian Advisor, DVM, Birmingham Zoo, USA Phil King: Assiniboine Park Zoo, Canada Reviewers: Dr. Mike Murray (Monterey Bay Aquarium, USA) John C. Anderson (Seattle Aquarium volunteer) Kristina Neuman (Point Blue Conservation Science) Sarah Saunders (Conservation Biology Graduate Program,University of Minnesota) AZA Staff Editors: Maya Seaman, MS, Animal Care Manual Editing Consultant Candice Dorsey, PhD, Director of Animal Programs Debborah Luke, PhD, Vice President, Conservation & Science Cover Photo Credits: Jeff Pribble Disclaimer: This manual presents a compilation of knowledge provided by recognized animal experts based on the current science, practice, and technology of animal management.
    [Show full text]
  • Compendium of Avian Ecology
    Compendium of Avian Ecology ZOL 360 Brian M. Napoletano All images taken from the USGS Patuxent Wildlife Research Center. http://www.mbr-pwrc.usgs.gov/id/framlst/infocenter.html Taxonomic information based on the A.O.U. Check List of North American Birds, 7th Edition, 1998. Ecological Information obtained from multiple sources, including The Sibley Guide to Birds, Stokes Field Guide to Birds. Nest and other images scanned from the ZOL 360 Coursepack. Neither the images nor the information herein be copied or reproduced for commercial purposes without the prior consent of the original copyright holders. Full Species Names Common Loon Wood Duck Gaviiformes Anseriformes Gaviidae Anatidae Gavia immer Anatinae Anatini Horned Grebe Aix sponsa Podicipediformes Mallard Podicipedidae Anseriformes Podiceps auritus Anatidae Double-crested Cormorant Anatinae Pelecaniformes Anatini Phalacrocoracidae Anas platyrhynchos Phalacrocorax auritus Blue-Winged Teal Anseriformes Tundra Swan Anatidae Anseriformes Anatinae Anserinae Anatini Cygnini Anas discors Cygnus columbianus Canvasback Anseriformes Snow Goose Anatidae Anseriformes Anatinae Anserinae Aythyini Anserini Aythya valisineria Chen caerulescens Common Goldeneye Canada Goose Anseriformes Anseriformes Anatidae Anserinae Anatinae Anserini Aythyini Branta canadensis Bucephala clangula Red-Breasted Merganser Caspian Tern Anseriformes Charadriiformes Anatidae Scolopaci Anatinae Laridae Aythyini Sterninae Mergus serrator Sterna caspia Hooded Merganser Anseriformes Black Tern Anatidae Charadriiformes Anatinae
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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).
    [Show full text]
  • 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.
    [Show full text]
  • Alpha Codes for 2168 Bird Species (And 113 Non-Species Taxa) in Accordance with the 62Nd AOU Supplement (2021), Sorted Taxonomically
    Four-letter (English Name) and Six-letter (Scientific Name) Alpha Codes for 2168 Bird Species (and 113 Non-Species Taxa) in accordance with the 62nd AOU Supplement (2021), sorted taxonomically Prepared by Peter Pyle and David F. DeSante The Institute for Bird Populations www.birdpop.org ENGLISH NAME 4-LETTER CODE SCIENTIFIC NAME 6-LETTER CODE Highland Tinamou HITI Nothocercus bonapartei NOTBON Great Tinamou GRTI Tinamus major TINMAJ Little Tinamou LITI Crypturellus soui CRYSOU Thicket Tinamou THTI Crypturellus cinnamomeus CRYCIN Slaty-breasted Tinamou SBTI Crypturellus boucardi CRYBOU Choco Tinamou CHTI Crypturellus kerriae CRYKER White-faced Whistling-Duck WFWD Dendrocygna viduata DENVID Black-bellied Whistling-Duck BBWD Dendrocygna autumnalis DENAUT West Indian Whistling-Duck WIWD Dendrocygna arborea DENARB Fulvous Whistling-Duck FUWD Dendrocygna bicolor DENBIC Emperor Goose EMGO Anser canagicus ANSCAN Snow Goose SNGO Anser caerulescens ANSCAE + Lesser Snow Goose White-morph LSGW Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Intermediate-morph LSGI Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Blue-morph LSGB Anser caerulescens caerulescens ANSCCA + Greater Snow Goose White-morph GSGW Anser caerulescens atlantica ANSCAT + Greater Snow Goose Intermediate-morph GSGI Anser caerulescens atlantica ANSCAT + Greater Snow Goose Blue-morph GSGB Anser caerulescens atlantica ANSCAT + Snow X Ross's Goose Hybrid SRGH Anser caerulescens x rossii ANSCAR + Snow/Ross's Goose SRGO Anser caerulescens/rossii ANSCRO Ross's Goose
    [Show full text]