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REVIEW Physiological Dependence on Copulation in Parthenogenetic Females Can Reduce the Cost of Sex
ANIMAL BEHAVIOUR, 2004, 67, 811e822 doi:10.1016/j.anbehav.2003.05.014 REVIEW Physiological dependence on copulation in parthenogenetic females can reduce the cost of sex M. NEIMAN Department of Biology, Indiana University, Bloomington (Received 6 December 2002; initial acceptance 10 April 2003; final acceptance 27 May 2003; MS. number: ARV-25) Despite the two-fold reproductive advantage of asexual over sexual reproduction, the majority of eukaryotic species are sexual. Why sex is so widespread is still unknown and remains one of the most important unanswered questions in evolutionary biology. Although there are several hypothesized mechanisms for the maintenance of sex, all require assumptions that may limit their applicability. I suggest that the maintenance of sex may be aided by the detrimental retention of ancestral traits related to sexual reproduction in the asexual descendants of sexual taxa. This reasoning is based on the fact that successful reproduction in many obligately sexual species is dependent upon the behavioural, physical and physiological cues that accompany sperm delivery. More specifically, I suggest that although parthenogenetic (asexual) females have no need for sperm per se, parthenogens descended from sexual ancestors may not be able to reach their full reproductive potential in the absence of the various stimuli provided by copulatory behaviour. This mechanism is novel in assuming no intrinsic advantage to producing genetically variable offspring; rather, sex is maintained simply through phylogenetic constraint. I review and synthesize relevant literature and data showing that access to males and copulation increases reproductive output in both sexual and parthenogenetic females. These findings suggest that the current predominance of sexual reproduction, despite its well-documented drawbacks, could in part be due to the retention of physiological dependence on copulatory stimuli in parthenogenetic females. -
The Seahorse Genome and the Evolution of Its Specialized
OPEN ARTICLE doi:10.1038/nature20595 The seahorse genome and the evolution of its specialized morphology Qiang Lin1*§, Shaohua Fan2†*, Yanhong Zhang1*, Meng Xu3*, Huixian Zhang1,4*, Yulan Yang3*, Alison P. Lee4†, Joost M. Woltering2, Vydianathan Ravi4, Helen M. Gunter2†, Wei Luo1, Zexia Gao5, Zhi Wei Lim4†, Geng Qin1,6, Ralf F. Schneider2, Xin Wang1,6, Peiwen Xiong2, Gang Li1, Kai Wang7, Jiumeng Min3, Chi Zhang3, Ying Qiu8, Jie Bai8, Weiming He3, Chao Bian8, Xinhui Zhang8, Dai Shan3, Hongyue Qu1,6, Ying Sun8, Qiang Gao3, Liangmin Huang1,6, Qiong Shi1,8§, Axel Meyer2§ & Byrappa Venkatesh4,9§ Seahorses have a specialized morphology that includes a toothless tubular mouth, a body covered with bony plates, a male brood pouch, and the absence of caudal and pelvic fins. Here we report the sequencing and de novo assembly of the genome of the tiger tail seahorse, Hippocampus comes. Comparative genomic analysis identifies higher protein and nucleotide evolutionary rates in H. comes compared with other teleost fish genomes. We identified an astacin metalloprotease gene family that has undergone expansion and is highly expressed in the male brood pouch. We also find that the H. comes genome lacks enamel matrix protein-coding proline/glutamine-rich secretory calcium-binding phosphoprotein genes, which might have led to the loss of mineralized teeth. tbx4, a regulator of hindlimb development, is also not found in H. comes genome. Knockout of tbx4 in zebrafish showed a ‘pelvic fin-loss’ phenotype similar to that of seahorses. Members of the teleost family Syngnathidae (seahorses, pipefishes de novo. The H. comes genome assembly is of high quality, as > 99% and seadragons) (Extended Data Fig. -
Reproductive Ecology & Sexual Selection
Reproductive Ecology & Sexual Selection REPRODUCTIVE ECOLOGY REPRODUCTION & SEXUAL SELECTION • Asexual • Sexual – Attraction, Courtship, and Mating – Fertilization – Production of Young The Evolutionary Enigma of Benefits of Asex Sexual Reproduction • Sexual reproduction produces fewer reproductive offspring than asexual reproduction, a so-called reproductive handicap 1. Eliminate problem to locate, court, & retain suitable mate. Asexual reproduction Sexual reproduction Generation 1 2. Doubles population growth rate. Female Female 3. Avoid “cost of meiosis”: Generation 2 – genetic representation in later generations isn't reduced by half each time Male 4. Preserve gene pool adapted to local Generation 3 conditions. Generation 4 Figure 23.16 The Energetic Costs of Sexual Reproduction Benefits of Sex • Allocation of Resources 1. Reinforcement of social structure 2. Variability in face of changing environment. – why buy four lottery tickets w/ the same number on them? Relative benefits: Support from organisms both asexual in constant & sexual in changing environments – aphids have wingless female clones & winged male & female dispersers – ciliates conjugate if environment is deteriorating Heyer 1 Reproductive Ecology & Sexual Selection Simultaneous Hermaphrodites TWO SEXES • Advantageous if limited mobility and sperm dispersal and/or low population density • Guarantee that any member of your species encountered is the • Conjugation “right” sex • Self fertilization still provides some genetic variation – Ciliate protozoans with + & - mating -
Revlined Seahorse Dad Copy
Diligent Dads In the wild animal world, there are a number of nurturing males, including the seahorse The lined seahorse gets its name from its vertical stripes. They can change colors to provide camouflage or denote mood. Photo credit: Linda De Volder By J. Morton Galetto, CU Maurice River When it comes to fathering, the animal world exhibits a spectrum from love ‘em and leave ‘em to champion surveillance. In honor of Father’s Day let’s discuss some superior dads. In the animal kingdom the emperor penguin male takes sole responsibility for incubating an egg. It is balanced on his feet which he shuffles along the ice of Antarctica for two months, enduring 125 mph winds and – 40 temperatures. Hundreds of huddling fathers bear this responsibility while their mates are at sea fattening-up. This story of dedication and endurance is powerful and heart-warming. Emperor penguins’ dedication leads them to be described as the #1 exemplary father in a multitude of articles. I highly recommend the 2005 film “March of the Penguins,” that documents this challenging fatherly devotion. In fact every dead-beat dad should be required to watch “March of the Penguins,” repeatedly, even if it doesn’t help. But our story is not about parental neglect; it is about celebrating great dads. Let’s bring it home a bit, since most of us will never visit Antarctica and certainly not in 125 mph winds. We’ll explore some local creatures and focus on one unexpected twist in fathering. In past articles we have discussed some dutiful parents of the avian variety. -
Courtship Behavior in the Dwarf Seahorse, Hippocampuszosterae
Copeia, 1996(3), pp. 634-640 Courtship Behavior in the Dwarf Seahorse, Hippocampuszosterae HEATHER D. MASONJONESAND SARA M. LEWIS The seahorse genus Hippocampus (Syngnathidae) exhibits extreme morpho- logical specialization for paternal care, with males incubating eggs within a highly vascularized brood pouch. Dwarf seahorses, H. zosterae, form monoga- mous pairs that court early each morning until copulation takes place. Daily behavioral observations of seahorse pairs (n = 15) were made from the day of introduction through the day of copulation. Four distinct phases of seahorse courtship are marked by prominent behavioral changes, as well as by differences in the intensity of courtship. The first courtship phase occurs for one or two mornings preceding the day of copulation and is characterized by reciprocal quivering, consisting of rapid side-to-side body vibrations displayed alternately by males and females. The remaining courtship phases are restricted to the day of copulation, with the second courtship phase distinguished by females pointing, during which the head is raised upward. In the third courtship phase, males begin to point in response to female pointing. During the final phase of courtship, seahorse pairs repeatedly rise together in the water column, eventually leading to females transferring their eggs directly into the male brood pouch during a brief midwater copulation. Courtship activity level (representing the percentage of time spent in courtship) increased from relatively low levels during the first courtship phase to highly active courtship on the day of copulation. Males more actively initiated courtship on the days preceding copulation, indicating that these seahorses are not courtship-role reversed, as has previously been assumed. -
Reproduction in Humans
P5/6 SCIENCE Reproduction In Humans Sexual reproduction does not only occur in plants. It also occurs in humans where the female reproductive cell and the male reproductive cell unite to form a new individual. Female Sex Organs The ovary is part of the female sex organ. There are two ovaries in each woman’s body. Ova (singular ovum) or eggs are the female sex cells. The ova are stored in the ovaries of a female. A female is born with all the unripe eggs (or ova) she will ever have in her lifetime. When she reaches puberty, an egg will start to mature in the ovary. Every month, an egg will be released by the ovary into one of the Fallopian tubes. This is called ovulation. On average, a female is born with approximately one million eggs but they decline in number and quality as she grows older. In fact, a girl is only left with about 400,000 eggs by the time she reaches puberty. Only a few hundred are released during ovulation. Fallopian tubes ovary uterus (womb) cervix vagina Female reproductive system Male Sex Organs A male has two sex organs. They are the testis and the penis. Sperms are the male sex cells. They are produced in the testes. When a boy reaches puberty, his testes will start to produce sperms. It takes about 72 days for a sperm to grow. urinary bladder (stores urine, not part of the reproductive system) sperm ducts testes penis Male reproductive system Taken from SCIENCE PARTNER: A Complete Guide To Upper Block Science © Singapore Asia Publishers Pte Ltd SAPSCSP5&6_W04 Website: www.sapgrp.com | Facebook: Singapore-Asia-Publishers Page 1/8 P5/6 SCIENCE Reproduction In Humans A sperm cell consists of a head (where the nucleus lies), the midpiece (which is the motor of the sperm) and a tail which helps it to swim. -
Marine Protected Species Identification Guide
Department of Primary Industries and Regional Development Marine protected species identification guide June 2021 Fisheries Occasional Publication No. 129, June 2021. Prepared by K. Travaille and M. Hourston Cover: Hawksbill turtle (Eretmochelys imbricata). Photo: Matthew Pember. Illustrations © R.Swainston/www.anima.net.au Bird images donated by Important disclaimer The Chief Executive Officer of the Department of Primary Industries and Regional Development and the State of Western Australia accept no liability whatsoever by reason of negligence or otherwise arising from the use or release of this information or any part of it. Department of Primary Industries and Regional Development Gordon Stephenson House 140 William Street PERTH WA 6000 Telephone: (08) 6551 4444 Website: dpird.wa.gov.au ABN: 18 951 343 745 ISSN: 1447 - 2058 (Print) ISBN: 978-1-877098-22-2 (Print) ISSN: 2206 - 0928 (Online) ISBN: 978-1-877098-23-9 (Online) Copyright © State of Western Australia (Department of Primary Industries and Regional Development), 2021. ii Marine protected species ID guide Contents About this guide �������������������������������������������������������������������������������������������1 Protected species legislation and international agreements 3 Reporting interactions ���������������������������������������������������������������������������������4 Marine mammals �����������������������������������������������������������������������������������������5 Relative size of cetaceans �������������������������������������������������������������������������5 -
Of the Americas
iSeahorse.org – Saving Seahorses Together seahorses of the Americas Seahorses of the Americas Masters of Disguise There are currently fi ve recognized species of Seahorses are well-camoufl aged, and individuals seahorses (Hippocampus spp.) in the Americas, can be covered by seaweeds and sediments in one in the Pacifi c Ocean and four in the the wild. Color and lengths of skin fi laments (“hairs”) Atlantic. All of these American seahorses tend can vary for individuals within the same species to live in relatively shallow coastal areas with and so are NOT useful for identifi cation. Practice 3D-structured habitat, including seagrasses, your identifi cation skills before starting surveys. corals, and mangroves. Above: Potential seahorse habitats. Left to right: coral reef, seagrass bed, mangrove forest. Photos by Tse-Lynn Loh and Ria Tan/Wild Singapore. Seahorse Parts Hippocampus barbouri Coronet Trunk Eye spine Nose spine Dorsal fi n Cheek spines Snout Brood pouch (males only) Tail Female Male In females, the belly does not extend past the bottom of the dorsal fi n. If you are uncertain, it is likely male. Pacifi c Seahorses Don’t Know Which Seahorse Species? How to Photograph for ID For unknown species, record the Head length following characteristics: • Torso length Torso length (distance from top of coronet to base of dorsal fi n) • Head length (from immediately behind the operculum – the fl ap covering the gills – to tip of snout) • Snout length Snout length (from bump immediately in front of the eye to tip of snout) or Take a photo of the side profi le of the seahorse with a ruler and calculate these measurements from the photo. -
Trivers' Parental Investment and Sexual Selection: the Sex That Invests Most in Reproduction Will Be the Choosier Sex
Recent research reveals In an astonishing study recently undertaken in Western Europe, the following facts emerged: Married females choose to have affairs with males who are dominant, older, more physically attractive, more symmetrical in appearance, and married; females are much more likely to have an affair if their mates are subordinate, younger, physically unattractive, or have asymmetrical features; cosmetic surgery to improve a male's looks doubles his chances of having an adulterous affair; the more attractive a male, the less attentive he is as a father; roughly one in three of the babies born in Western Europe is the product of an adulterous affair. Why Have Sex? (I) We are involved in an “evolutionary arms race” against pathogens who reproduce faster than we do and therefore can modify their genetic structure to overcome our immune system. Sex allows us to modify our genetic structure, through our offspring, to win (for a time) this battle. Lifjeld and colleagues’ findings are yet another illustration of the fact that sex has one killer advantage over other, more efficient means of reproduction. By mixing the genes of two individuals, sex creates a third - the offspring - with a new, unique combination. This maintains genetic variation, fuelling evolution and keeping one step ahead of agents of infectious disease. As evolutionary biologist Jonathan Howard put it: if sex causes disease, then it might also be true that disease causes sex. (Nature 296-299 (2000) 1 Why Have Sex? (II) • Muller’s ratchet and Kondrashov’s solution • Deleterious mutations increase simply as the number of genes in an organism increases. -
An Invitation to Monitor Georgia's Coastal Wetlands
An Invitation to Monitor Georgia’s Coastal Wetlands www.shellfish.uga.edu By Mary Sweeney-Reeves, Dr. Alan Power, & Ellie Covington First Printing 2003, Second Printing 2006, Copyright University of Georgia “This book was prepared by Mary Sweeney-Reeves, Dr. Alan Power, and Ellie Covington under an award from the Office of Ocean and Coastal Resource Management, National Oceanic and Atmospheric Administration. The statements, findings, conclusions, and recommendations are those of the authors and do not necessarily reflect the views of OCRM and NOAA.” 2 Acknowledgements Funding for the development of the Coastal Georgia Adopt-A-Wetland Program was provided by a NOAA Coastal Incentive Grant, awarded under the Georgia Department of Natural Resources Coastal Zone Management Program (UGA Grant # 27 31 RE 337130). The Coastal Georgia Adopt-A-Wetland Program owes much of its success to the support, experience, and contributions of the following individuals: Dr. Randal Walker, Marie Scoggins, Dodie Thompson, Edith Schmidt, John Crawford, Dr. Mare Timmons, Marcy Mitchell, Pete Schlein, Sue Finkle, Jenny Makosky, Natasha Wampler, Molly Russell, Rebecca Green, and Jeanette Henderson (University of Georgia Marine Extension Service); Courtney Power (Chatham County Savannah Metropolitan Planning Commission); Dr. Joe Richardson (Savannah State University); Dr. Chandra Franklin (Savannah State University); Dr. Dionne Hoskins (NOAA); Dr. Charles Belin (Armstrong Atlantic University); Dr. Merryl Alber (University of Georgia); (Dr. Mac Rawson (Georgia Sea Grant College Program); Harold Harbert, Kim Morris-Zarneke, and Michele Droszcz (Georgia Adopt-A-Stream); Dorset Hurley and Aimee Gaddis (Sapelo Island National Estuarine Research Reserve); Dr. Charra Sweeney-Reeves (All About Pets); Captain Judy Helmey (Miss Judy Charters); Jan Mackinnon and Jill Huntington (Georgia Department of Natural Resources). -
Multiple Mating and Its Relationship to Alternative Modes of Gestation in Male-Pregnant Versus Female-Pregnant fish Species
Multiple mating and its relationship to alternative modes of gestation in male-pregnant versus female-pregnant fish species John C. Avise1 and Jin-Xian Liu Department of Ecology and Evolutionary Biology, University of California, Irvine, CA 92697 Contributed by John C. Avise, September 28, 2010 (sent for review August 20, 2010) We construct a verbal and graphical theory (the “fecundity-limitation within which he must incubate the embryos that he has sired with hypothesis”) about how constraints on the brooding space for em- one or more mates (14–17). This inversion from the familiar bryos probably truncate individual fecundity in male-pregnant and situation in female-pregnant animals apparently has translated in female-pregnant species in ways that should differentially influence some but not all syngnathid species into mating systems char- selection pressures for multiple mating by males or by females. We acterized by “sex-role reversal” (18, 19): a higher intensity of then review the empirical literature on genetically deduced rates of sexual selection on females than on males and an elaboration of fi multiple mating by the embryo-brooding parent in various fish spe- sexual secondary traits mostly in females. For one such pipe sh cies with three alternative categories of pregnancy: internal gesta- species, researchers also have documented that the sexual- tion by males, internal gestation by females, and external gestation selection gradient for females is steeper than that for males (20). More generally, fishes should be excellent subjects for as- (in nests) by males. Multiple mating by the brooding gender was fl common in all three forms of pregnancy. -
Seahorse Manual
Seahorse Manual 2010 Seahorse Manual ___________________________ David Garcia SEA LIFE Hanover, Germany Neil Garrick-Maidment The Seahorse Trust, England Seahorses are a very challenging species in husbandry and captive breeding terms and over the years there have been many attempts to keep them using a variety of methods. It is Sealife and The Seahorse Trust’s long term intention to be completely self-sufficient in seahorses and this manual has been put together to be used, to make this long term aim a reality. The manual covers all subjects necessary to keep seahorses from basic husbandry to indepth captive breeding. It is to be used throughout the Sealife group and is to act as a guide to aquarist’s intent on good husbandry of seahorses. This manual covers all aspects from basic set, up, water parameters, transportation, husbandry, to food types and preparation for all stages of seahorse life, from fry to adult. By including contact points it will allow for feedback, so that experience gained can be included in further editions, thus improving seahorse husbandry. Corresponding authors: David Garcia: [email protected] N. Garrick-Maidment email: [email protected] Keywords: Seahorses, Hippocampus species, Zostera marina, seagrass, home range, courtship, reproduction,, tagging, photoperiod, Phytoplankton, Zooplankton, Artemia, Rotifers, lighting, water, substrate, temperature, diseases, cultures, Zoe Marine, Selco, decapsulation, filtration, enrichment, gestation. Seahorse Manual 2010 David Garcia SEA LIFE Hanover,