Animal Cells Usually Have an Irregular Shape, and Plant Cells Usually Have a Regular Shape
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
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. -
Sex-Specific Spawning Behavior and Its Consequences in an External Fertilizer
vol. 165, no. 6 the american naturalist june 2005 Sex-Specific Spawning Behavior and Its Consequences in an External Fertilizer Don R. Levitan* Department of Biological Science, Florida State University, a very simple way—the timing of gamete release (Levitan Tallahassee, Florida 32306-1100 1998b). This allows for an investigation of how mating behavior can influence mating success without the com- Submitted October 29, 2004; Accepted February 11, 2005; Electronically published April 4, 2005 plications imposed by variation in adult morphological features, interactions within the female reproductive sys- tem, or post-mating (or pollination) investments that can all influence paternal and maternal success (Arnqvist and Rowe 1995; Havens and Delph 1996; Eberhard 1998). It abstract: Identifying the target of sexual selection in externally also provides an avenue for exploring how the evolution fertilizing taxa has been problematic because species in these taxa often lack sexual dimorphism. However, these species often show sex of sexual dimorphism in adult traits may be related to the differences in spawning behavior; males spawn before females. I in- evolutionary transition to internal fertilization. vestigated the consequences of spawning order and time intervals One of the most striking patterns among animals and between male and female spawning in two field experiments. The in particular invertebrate taxa is that, generally, species first involved releasing one female sea urchin’s eggs and one or two that copulate or pseudocopulate exhibit sexual dimor- males’ sperm in discrete puffs from syringes; the second involved phism whereas species that broadcast gametes do not inducing males to spawn at different intervals in situ within a pop- ulation of spawning 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. -
Coleoptera, Chrysomelidae, Galerucinae)
A peer-reviewed open-access journal ZooKeys 720:Traumatic 77–89 (2017) mating by hand saw-like spines on the internal sac in Pyrrhalta maculicollis 77 doi: 10.3897/zookeys.720.13015 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Traumatic mating by hand saw-like spines on the internal sac in Pyrrhalta maculicollis (Coleoptera, Chrysomelidae, Galerucinae) Yoko Matsumura1, Haruki Suenaga2, Yoshitaka Kamimura3, Stanislav N. Gorb1 1 Department of Functional Morphology and Biomechanics, Zoological Institute, Kiel University, Am Botani- schen Garten 1-9, D-24118 Kiel, Germany 2 Sunshine A205, Nishiachi-chô 833-8, Kurashiki-shi, Okayama Pref., 710-0807, Japan 3 Department of Biology, Keio University, 4-1-1 Hiyoshi, Yokohama 223-8521, Japan Corresponding author: Yoko Matsumura ([email protected]) Academic editor: Michael Schmitt | Received 1 April 2017 | Accepted 13 June 2017 | Published 11 December 2017 http://zoobank.org/BCF55DA6-95FB-4EC0-B392-D2C4B99E2C31 Citation: Matsumura Y, Suenaga H, Kamimura Y, Gorb SN (2017) Traumatic mating by hand saw-like spines on the internal sac in Pyrrhalta maculicollis (Coleoptera, Chrysomelidae, Galerucinae). In: Chaboo CS, Schmitt M (Eds) Research on Chrysomelidae 7. ZooKeys 720: 77–89. https://doi.org/10.3897/zookeys.720.13015 Abstract Morphology of the aedeagus and vagina of Pyrrhalta maculicollis and its closely related species were inves- tigated. The internal sac of P. maculicollis bears hand saw-like spines, which are arranged in a row. Healing wounds were found on the vagina of this species, whose females were collected in the field during a repro- ductive season. However, the number of the wounds is low in comparison to the number of the spines. -
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. -
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 -
Coevolution of Male and Female Genital Morphology in Waterfowl Patricia L
Coevolution of Male and Female Genital Morphology in Waterfowl Patricia L. R. Brennan1,2*, Richard O. Prum1, Kevin G. McCracken3, Michael D. Sorenson4, Robert E. Wilson3, Tim R. Birkhead2 1 Department of Ecology and Evolutionary Biology, and Peabody Natural History Museum, Yale University, New Haven, Connecticut, United States of America, 2 Department of Animal and Plant Sciences, University of Sheffield, Western Bank, Sheffield, United Kingdom, 3 Institute of Arctic Biology, Department of Biology and Wildlife, and University of Alaska Museum, University of Alaska Fairbanks, Fairbanks, Alaska, United States of America, 4 Department of Biology, Boston University, Boston, Massachusetts, United States of America Most birds have simple genitalia; males lack external genitalia and females have simple vaginas. However, male waterfowl have a phallus whose length (1.5–.40 cm) and morphological elaborations vary among species and are positively correlated with the frequency of forced extra-pair copulations among waterfowl species. Here we report morphological complexity in female genital morphology in waterfowl and describe variation vaginal morphology that is unprecedented in birds. This variation comprises two anatomical novelties: (i) dead end sacs, and (ii) clockwise coils. These vaginal structures appear to function to exclude the intromission of the counter-clockwise spiralling male phallus without female cooperation. A phylogenetically controlled comparative analysis of 16 waterfowl species shows that the degree of vaginal elaboration is positively correlated with phallus length, demonstrating that female morphological complexity has co-evolved with male phallus length. Intersexual selection is most likely responsible for the observed coevolution, although identifying the specific mechanism is difficult. Our results suggest that females have evolved a cryptic anatomical mechanism of choice in response to forced extra-pair copulations. -
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. -
Ultrastructural Observations of the Argonaut Shell
Scanning Microscopy Volume 8 Number 1 Article 4 2-15-1994 Ultrastructural Observations of the Argonaut Shell P. R. Mitchell Monash University, Australia P. P. Phakey Monash University, Australia W. A. Rachinger Monash University, Australia Follow this and additional works at: https://digitalcommons.usu.edu/microscopy Part of the Biology Commons Recommended Citation Mitchell, P. R.; Phakey, P. P.; and Rachinger, W. A. (1994) "Ultrastructural Observations of the Argonaut Shell," Scanning Microscopy: Vol. 8 : No. 1 , Article 4. Available at: https://digitalcommons.usu.edu/microscopy/vol8/iss1/4 This Article is brought to you for free and open access by the Western Dairy Center at DigitalCommons@USU. It has been accepted for inclusion in Scanning Microscopy by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. Scanning Microscopy, Vol. 8, No. 1, 1994 (Pages 35-46) 0891- 7035/94$5. 00 +. 25 Scanning Microscopy International, Chicago (AMF O'Hare), IL 60666 USA ULTRASTRUCTURAL OBSERVATIONS OF THE ARGONAUT SHELL P. R. Mitchell, P. P. Phakey*, W. A. Rachinger Department of Physics, Monash University, Wellington Road, Clayton, Victoria 3168, Australia (Received for publication October 6, 1993, and in revised form February 15, 1994) Abstract Introduction An examination of the ultrastructure of the shell of the The Nautilus and the Argonaut are the only two cephalopod Argonauta Nodosa was carried out using scanning cephalopods to possess external shells, however, despite a electron microscopy, transmission electron microscopy and superficial similarity in shape, the shells have very little in polarised light microscopy. The structure of the Argonaut common. The shell of the Argonaut is thin and fragile with shell was found to consist of an inner and outer prismatic no internal partitions or chambers and, in evolutionary terms, layer separated by a thin central zone which was sparsely is a relatively recent addition [Young, 1959, Wells, 1962, occupied by spherulitic crystals. -
THE 7TH ANNUAL May 3, 2019 MAY 3, 2019
THE 7TH ANNUAL May 3, 2019 MAY 3, 2019 Schedule 2:00 - 3:00 p.m. Keynote Speaker 3:00 - 3:55 p.m. Poster Session I 4:05 - 5:00 p.m. Poster Session II Awards for Best poster presentations will Be announced immediately following the poster sessions. Symposium Organizers: Dr. Eric Freundt, Dr. Simon Schuler, Olivia Crimbly, and Devon Grey. The CNHS Undergraduate Research Symposium provides an opportunity for students within the College of Natural and Health Sciences to present their current or recently completed research projects in a poster format. The research may have been performed as part of a course, an Honors Research Fellowship, or an independent project conducted with a faculty mentor. ABstracts for all poster presentations are included in this booklet and are listed in alphabetical order based on the presenting author’s last name. The Symposium was initiated in 2013 through a generous grant from the UT Board of Fellows. Further financial support from the Office of the Dean of CNHS, the Department of Biology and Department of Chemistry, Biochemistry and Physics is also acknowledged. Finally, the organizers would like to thank all presenters, faculty mentors, and faculty judges for their participation in this event. 1 Keynote Speaker Florida Red Tide: What's new, what's true, and what you should know. Dr. Cynthia Heil Director, Red Tide Institute Mote Marine LaBoratory 2 Poster Session I * Denotes authors presenting at symposium (1) Isolation of Marine Sediment-Derived Bacteria that (8) Does Response of Weekly Strength Training Volume on Produce Biologically Active Metabolites Muscular Hypertrophic Adaptations in Trained GaBriella AlBert*1and Dr. -
Argonaut Octopus
Rare Discovery: Tropical Octopus Caught in Los Angeles Becky Oskin, OurAmazingPlanet Staff Writer - Oct 18, 2012 A female argonaut ― an octopus also called a paper nautilus ― is recuperating at the Cabrillo Marine Aquarium CREDIT: Gary Florin, Cabrillo Marine Aquarium. Warm ocean currents off the coast of Southern California delivered a surprise to a couple of squid fishermen this past weekend. A female argonaut ― an octopus also called a paper nautilus ― turned up in their bait box, The Daily Breeze reported Oct. 16. The men recognized the rare find and turned it over to the Cabrillo Marine Aquarium, said Kiersten Darrow, the aquarium's research curator. Argonauts live near the surface of the open ocean, unlike most other octopuses, which live near the bottom. The argonauts secrete thin, translucent shells that hold pockets of air, helping them float. Their normal range is the warm water along the equator, especially near Indonesia and the Philippines, Darrow told OurAmazingPlanet. "I've never seen anything quite like this," she said of the California find. "I've never seen anything quite like this," she said of the California find. The silvery, baseball-size animal the fishermen caught has eight tentacles, big eyes and the color-changing abilities characteristic of an octopus. Its size means it's probably a full-grown adult, Darrow said. In one of the aquarium's Jacuzzi-sized tanks, the octopus is now exploring its surroundings, flashing gold when it sees an overhead light or purple when it's in darker water, Darrow said. "A couple of times, it's reached out its tentacles and explored around the tank, touching the different walls, especially if we have food sitting on the bottom of the tank.