Hippocampus Zosterae) As Threatened Or Endangered Under the Endangered Species Act
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Freshwater Ornamental Fish Commonly Cultured in Florida 1 Jeffrey E
Circular 54 Freshwater Ornamental Fish Commonly Cultured in Florida 1 Jeffrey E. Hill and Roy P.E. Yanong2 Introduction Unlike many traditional agriculture industries in Florida which may raise one or only a few different species, tropical Freshwater tropical ornamental fish culture is the largest fish farmers collectively culture hundreds of different component of aquaculture in the State of Florida and ac- species and varieties of fishes from numerous families and counts for approximately 95% of all ornamentals produced several geographic regions. There is much variation within in the US. There are about 200 Florida producers who and among fish groups with regard to acceptable water collectively raise over 800 varieties of freshwater fishes. In quality parameters, feeding and nutrition, and mode of 2003 alone, farm-gate value of Florida-raised tropical fish reproduction. Some farms specialize in one or a few fish was about US$47.2 million. Given the additional economic groups, while other farms produce a wide spectrum of effects of tropical fish trade such as support industries, aquatic livestock. wholesalers, retail pet stores, and aquarium product manufacturing, the importance to Florida is tremendous. Fish can be grouped in a number of different ways. One major division in the industry which has practical signifi- Florida’s tropical ornamental aquaculture industry is cance is that between egg-laying species and live-bearing concentrated in Hillsborough, Polk, and Miami-Dade species. The culture practices for each division are different, counties with additional farms throughout the southern requiring specialized knowledge and equipment to succeed. half of the state. Historic factors, warm climate, the proxim- ity to airports and other infrastructural considerations This publication briefly reviews the more common groups (ready access to aquaculture equipment, supplies, feed, etc.) of freshwater tropical ornamental fishes cultured in Florida are the major reasons for this distribution. -
Hormone-Induced Spawning of Cultured Tropical Finfishes
ADVANCES IN TROPICAL AQUACULTURE. Tahiti, Feb. 20 - March 4 1989 AQUACOP 1FREMER Acres de Colloque 9 pp. 519 F39 49 Hormone-induced spawning of cultured tropical finfishes C.L. MARTE Southeast Asian Fisheries Development Genie. Aquaculture Department, Tig- bauan, ILOILO, Philippines Abstract — Commercially important tropical freshwater and marine finfishes are commonly spawned with pituitary homogenate, human chorionic gonadotropin (HCG) and semi-purified fish gonadotropins. These preparations are often adminis- tered in two doses, a lower priming dose followed a few hours later by a higher resolving dose. Interval between the first and second injections may vary from 3 - 24 hours depending on the species. Variable doses are used even for the same species and may be due to variable potencies of the gonadotropin preparations. Synthetic analogues of luteinizing hormone-releasing hormone (LHRHa) are becoming widely used for inducing ovulation and spawning in a variety of teleosts. For marine species such as milkfish, mullet, sea bass, and rabbitfish, a single LHRHa injection or pellet implant appears to be effective. Multiple spawnings of sea bass have also been obtained following a single injection or pellet implant of a high dose of LHRHa. In a number of freshwater fishes such as the cyprinids, LHRHa alone however has limited efficacy. Standardized methods using LHRHa together with the dopamine antagonists pimozide, domperidone and reserpine have been developed for various species of carps. The technique may also be applicable for spawning marine teleosts that may not respond to LHRHa alone or where a high dose of the peptide is required. Although natural spawning is the preferred method for breeding cultivated fish, induced spawning may be necessary to control timing and synchrony of egg production for practical reasons. -
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. -
Courtship & Mating Reproduction in Insects
Reproduction Courtship & Mating in Insects • How do the sexes find each other? – Light – Swarming (male only/ female only) – Leks (male aggregations) • Defend territory against males • Court arriving females – Pheromones What do they do once they find each other? Courtship • Close range intersexual behavior that induces sexual receptivity before and during mating. • Allows mate choice among and within species. 1 Types of Courtship • Visual displays Nuptial Gifts • Ritualized movements • 3 forms • Sound production – Cannibalization of males • Tactile stimulation – Glandular product • Nuptial gifts – Nuptial gift • Prey • Salt, nutrients Evolution of nuptial feeding Sexual Cannibalization • Female advantages • Rather extreme – Nutritional benefit • Male actually does not – Mate choice (mate with good provider) willingly give himself • Male advantages up… – Helping provision/produce his offspring – Where would its potential – Female returns sperm while feeding rather than reproductive benefit be? mating with someone else • Do females have • Male costs increased reproductive – Capturing food costs energy and incurs predation success? risk – Prey can be stolen and used by another male. 2 Glandular gifts Nuptial gifts • Often part of the spermatophore (sperm transfer unit) – Occupy female while sperm is being transferred – Parental investment by male • Generally a food item (usually prey) • Also regurgitations (some flies) • But beware the Cubic Zirconia, ladies Sexual selection Types of sexual selection • Intrasexual selection – Contest competition -
Fishes of Terengganu East Coast of Malay Peninsula, Malaysia Ii Iii
i Fishes of Terengganu East coast of Malay Peninsula, Malaysia ii iii Edited by Mizuki Matsunuma, Hiroyuki Motomura, Keiichi Matsuura, Noor Azhar M. Shazili and Mohd Azmi Ambak Photographed by Masatoshi Meguro and Mizuki Matsunuma iv Copy Right © 2011 by the National Museum of Nature and Science, Universiti Malaysia Terengganu and Kagoshima University Museum All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means without prior written permission from the publisher. Copyrights of the specimen photographs are held by the Kagoshima Uni- versity Museum. For bibliographic purposes this book should be cited as follows: Matsunuma, M., H. Motomura, K. Matsuura, N. A. M. Shazili and M. A. Ambak (eds.). 2011 (Nov.). Fishes of Terengganu – east coast of Malay Peninsula, Malaysia. National Museum of Nature and Science, Universiti Malaysia Terengganu and Kagoshima University Museum, ix + 251 pages. ISBN 978-4-87803-036-9 Corresponding editor: Hiroyuki Motomura (e-mail: [email protected]) v Preface Tropical seas in Southeast Asian countries are well known for their rich fish diversity found in various environments such as beautiful coral reefs, mud flats, sandy beaches, mangroves, and estuaries around river mouths. The South China Sea is a major water body containing a large and diverse fish fauna. However, many areas of the South China Sea, particularly in Malaysia and Vietnam, have been poorly studied in terms of fish taxonomy and diversity. Local fish scientists and students have frequently faced difficulty when try- ing to identify fishes in their home countries. During the International Training Program of the Japan Society for Promotion of Science (ITP of JSPS), two graduate students of Kagoshima University, Mr. -
Hippocampus Bargibanti Whitley 1970
Order Gasterosteiformes / Family Syngnathidae CITES Appendix II Hippocampus bargibanti Whitley 1970 Common names Bargibant’s seahorse (U.S.A.); pygmy seahorse (Australia) Synonyms None known Description Maximum recorded adult height: 2.4 cm45 Trunk rings: 11–12 Tail rings: 31–32 (31–33) HL/SnL: 4.6 (4.3–5.4) Rings supporting dorsal fin: 3 trunk rings (no tail rings) Dorsal fin rays: 14 (13–15) Pectoral fin rays: 10 (10–11) Coronet: Rounded knob Spines: Irregular bulbous tubercles scattered over body and tail; single, prominent rounded eye spine; single, low rounded cheek spine Other distinctive characteristics: Head and body fleshy, mostly without recognisable body rings; ventral portion of trunk segments incomplete; snout extremely short 30 Order Gasterosteiformes / Family Syngnathidae CITES Appendix II Colour/pattern: Two colour morphs are known: (a) pale grey or purple with pink or red tubercles (found on gorgonian coral Muricella plectana); and (b) yellow with orange tubercles (found on gorgonian coral Muricella paraplectana) Confirmed distribution Australia; France (New Caledonia); Indonesia; Japan; Papua New Guinea; Philippines Suspected distribution Federated States of Micronesia; Malaysia; Palau; Solomon Islands; Vanuatu Habitat Typically found at 16–40 m depth46; only known to occur on gorgonian corals of the genus Muricella45, 46 Life history Breeding season year round47; adults usually found in pairs or clusters of pairs in the wild (up to 28 on a single gorgonian)47; gestation duration averages 2 weeks48; length at birth averages 2 mm48; brood size 34 from one male47 Trade Not known in international trade Conservation status The entire genus Hippocampus is listed in Appendix II of CITES, effective May 20041. -
Teleostei, Syngnathidae)
ZooKeys 934: 141–156 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.934.50924 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae) Graham Short1,2,3, Louw Claassens4,5,6, Richard Smith4, Maarten De Brauwer7, Healy Hamilton4,8, Michael Stat9, David Harasti4,10 1 Research Associate, Ichthyology, Australian Museum Research Institute, Sydney, Australia 2 Ichthyology, California Academy of Sciences, San Francisco, USA 3 Ichthyology, Burke Museum, Seattle, USA 4 IUCN Seahorse, Pipefish Stickleback Specialist Group, University of British Columbia, Vancouver, Canada5 Rhodes University, Grahamstown, South Africa 6 Knysna Basin Project, Knysna, South Africa 7 University of Leeds, Leeds, UK 8 NatureServe, Arlington, Virginia, USA 9 University of Newcastle, Callaghan, NSW, Australia 10 Port Stephens Fisheries Institute, NSW, Australia Corresponding author: Graham Short ([email protected]) Academic editor: Nina Bogutskaya | Received 13 February 2020 | Accepted 12 April 2020 | Published 19 May 2020 http://zoobank.org/E9104D84-BB71-4533-BB7A-2DB3BD4E4B5E Citation: Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141–156. https://doi.org/10.3897/zookeys.934.50924 Abstract A new species and the first confirmed record of a true pygmy seahorse from Africa,Hippocampus nalu sp. nov., is herein described on the basis of two specimens, 18.9–22 mm SL, collected from flat sandy coral reef at 14–17 meters depth from Sodwana Bay, South Africa. -
Early Life History of Syngnathus Abaster
Journal of Fish Biology (2006) 68, 80–86 doi:10.1111/j.1095-8649.2005.00878.x,availableonlineathttp://www.blackwell-synergy.com Early life history of Syngnathus abaster K. SILVA*†‡, N. M. MONTEIRO*†, V. C. ALMADA§ AND M. N. VIEIRA*† *Departamento de Zoologia e Antropologia da Faculdade de Cieˆncias da Universidade do Porto, Prac¸ a Gomes Teixeira, 4099-002 Porto, Portugal,†CIIMAR, Rua dos Bragas 177, 4050-123 Porto, Portugal and §ISPA, Rua Jardim do Tabaco 34, 1149-041 Lisboa, Portugal (Received 2 February 2005, Accepted 15 June 2005) The embryonic and larval development of the pipefish Syngnathus abaster is described, based on ex situ observations. The full development sequence lasted 24–32 days (at 18–19 C), which was shortened to 21 days at higher temperatures (21–22 C). Newborn juveniles, with a uniform dark brown colouration, immediately assumed a benthic spatial distribution. This vertical distribution pattern remained unchanged at least during the first 4 weeks, after the release from the marsupium. The apparent absence of a pelagic life phase might have important repercussions in terms of population connectivity given increasing fragmentation and degrada- tion of the eelgrass habitat in the species’ range. # 2006 The Fisheries Society of the British Isles INTRODUCTION The Syngnathidae (pipefishes, pipehorses, seadragons and seahorses) exhibits one of the most specialized forms of parental care, with females depositing eggs in a specialized incubating area, located either on the abdomen (Gastrophori) or tail (Urophori) of the males (Herald, 1959). Even though male pregnancy is a widespread characteristic in all syngnathids, the anatomical complexity of the brooding structures varies among species, from the simplest incubating ventral surface of the Nerophinae, where eggs are glued without any protective plates or membranes, to the Hippocampinae sealed brood pouch. -
Reproductive Biology of the Opossum Pipefish, Microphis Brachyurus Lineatus, in Tecolutla Estuary, Veracruz, Mexico
Gulf and Caribbean Research Volume 16 Issue 1 January 2004 Reproductive Biology of the Opossum Pipefish, Microphis brachyurus lineatus, in Tecolutla Estuary, Veracruz, Mexico Martha Edith Miranda-Marure Universidad Nacional Autonoma de Mexico Jose Antonio Martinez-Perez Universidad Nacional Autonoma de Mexico Nancy J. Brown-Peterson University of Southern Mississippi, [email protected] Follow this and additional works at: https://aquila.usm.edu/gcr Part of the Marine Biology Commons Recommended Citation Miranda-Marure, M. E., J. A. Martinez-Perez and N. J. Brown-Peterson. 2004. Reproductive Biology of the Opossum Pipefish, Microphis brachyurus lineatus, in Tecolutla Estuary, Veracruz, Mexico. Gulf and Caribbean Research 16 (1): 101-108. Retrieved from https://aquila.usm.edu/gcr/vol16/iss1/17 DOI: https://doi.org/10.18785/gcr.1601.17 This Article is brought to you for free and open access by The Aquila Digital Community. It has been accepted for inclusion in Gulf and Caribbean Research by an authorized editor of The Aquila Digital Community. For more information, please contact [email protected]. Gulf and Caribbean Research Vol 16, 101–108, 2004 Manuscript received September 25, 2003; accepted December 12, 2003 REPRODUCTIVE BIOLOGY OF THE OPOSSUM PIPEFISH, MICROPHIS BRACHYURUS LINEATUS, IN TECOLUTLA ESTUARY, VERACRUZ, MEXICO Martha Edith Miranda-Marure, José Antonio Martínez-Pérez, and Nancy J. Brown-Peterson1 Laboratorio de Zoología, Universidad Nacional Autónoma de México, Facultad de Estudios Superiores Iztacala. Av., de los Barrios No.1, Los Reyes Iztacala, Tlalnepantla, Estado de México, C.P. 05490 Mexico 1Department of Coastal Sciences, The University of Southern Mississippi, 703 East Beach Drive, Ocean Springs, MS 39564 USA ABSTRACT The reproductive biology of the opossum pipefish, Microphis brachyurus lineatus, was investigated in Tecolutla estuary, Veracruz, Mexico, to determine sex ratio, size at maturity, gonadal and brood pouch histology, reproductive seasonality, and fecundity of this little-known syngnathid. -
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.