Reproduction in Plants and Animals
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Reference Sheet 1
MALE SEXUAL SYSTEM 8 7 8 OJ 7 .£l"00\.....• ;:; ::>0\~ <Il '"~IQ)I"->. ~cru::>s ~ 6 5 bladder penis prostate gland 4 scrotum seminal vesicle testicle urethra vas deferens FEMALE SEXUAL SYSTEM 2 1 8 " \ 5 ... - ... j 4 labia \ ""\ bladderFallopian"k. "'"f"";".'''¥'&.tube\'WIT / I cervixt r r' \ \ clitorisurethrauterus 7 \ ~~ ;~f4f~ ~:iJ 3 ovaryvagina / ~ 2 / \ \\"- 9 6 adapted from F.L.A.S.H. Reproductive System Reference Sheet 3: GLOSSARY Anus – The opening in the buttocks from which bowel movements come when a person goes to the bathroom. It is part of the digestive system; it gets rid of body wastes. Buttocks – The medical word for a person’s “bottom” or “rear end.” Cervix – The opening of the uterus into the vagina. Circumcision – An operation to remove the foreskin from the penis. Cowper’s Glands – Glands on either side of the urethra that make a discharge which lines the urethra when a man gets an erection, making it less acid-like to protect the sperm. Clitoris – The part of the female genitals that’s full of nerves and becomes erect. It has a glans and a shaft like the penis, but only its glans is on the out side of the body, and it’s much smaller. Discharge – Liquid. Urine and semen are kinds of discharge, but the word is usually used to describe either the normal wetness of the vagina or the abnormal wetness that may come from an infection in the penis or vagina. Duct – Tube, the fallopian tubes may be called oviducts, because they are the path for an ovum. -
History Department Botany
THE HISTORY OF THE DEPARTMENT OF BOTANY 1889-1989 UNIVERSITY OF MINNESOTA SHERI L. BARTLETT I - ._-------------------- THE HISTORY OF THE DEPARTMENT OF BOTANY 1889-1989 UNIVERSITY OF MINNESOTA SHERI L. BARTLETT TABLE OF CONTENTS Preface 1-11 Chapter One: 1889-1916 1-18 Chapter Two: 1917-1935 19-38 Chapter Three: 1936-1954 39-58 Chapter Four: 1955-1973 59-75 Epilogue 76-82 Appendix 83-92 Bibliography 93-94 -------------------------------------- Preface (formerly the College of Science, Literature and the Arts), the College of Agriculture, or The history that follows is the result some other area. Eventually these questions of months ofresearch into the lives and work were resolved in 1965 when the Department of the Botany Department's faculty members joined the newly established College of and administrators. The one-hundred year Biological Sciences (CBS). In 1988, The overview focuses on the Department as a Department of Botany was renamed the whole, and the decisions that Department Department of Plant Biology, and Irwin leaders made to move the field of botany at Rubenstein from the Department of Genetics the University of Minnesota forward in a and Cell Biology became Plant Biology's dynamic and purposeful manner. However, new head. The Department now has this is not an effort to prove that the administrative ties to both the College of Department's history was linear, moving Biological Sciences and the College of forward in a pre-determined, organized Agriculture. fashion at every moment. Rather I have I have tried to recognize the attempted to demonstrate the complexities of accomplishments and individuality of the the personalities and situations that shaped Botany Department's faculty while striving to the growth ofthe Department and made it the describe the Department as one entity. -
Reproduction in Plants Which But, She Has Never Seen the Seeds We Shall Learn in This Chapter
Reproduction in 12 Plants o produce its kind is a reproduction, new plants are obtained characteristic of all living from seeds. Torganisms. You have already learnt this in Class VI. The production of new individuals from their parents is known as reproduction. But, how do Paheli thought that new plants reproduce? There are different plants always grow from seeds. modes of reproduction in plants which But, she has never seen the seeds we shall learn in this chapter. of sugarcane, potato and rose. She wants to know how these plants 12.1 MODES OF REPRODUCTION reproduce. In Class VI you learnt about different parts of a flowering plant. Try to list the various parts of a plant and write the Asexual reproduction functions of each. Most plants have In asexual reproduction new plants are roots, stems and leaves. These are called obtained without production of seeds. the vegetative parts of a plant. After a certain period of growth, most plants Vegetative propagation bear flowers. You may have seen the It is a type of asexual reproduction in mango trees flowering in spring. It is which new plants are produced from these flowers that give rise to juicy roots, stems, leaves and buds. Since mango fruit we enjoy in summer. We eat reproduction is through the vegetative the fruits and usually discard the seeds. parts of the plant, it is known as Seeds germinate and form new plants. vegetative propagation. So, what is the function of flowers in plants? Flowers perform the function of Activity 12.1 reproduction in plants. Flowers are the Cut a branch of rose or champa with a reproductive parts. -
Revised Glossary for AQA GCSE Biology Student Book
Biology Glossary amino acids small molecules from which proteins are A built abiotic factor physical or non-living conditions amylase a digestive enzyme (carbohydrase) that that affect the distribution of a population in an breaks down starch ecosystem, such as light, temperature, soil pH anaerobic respiration respiration without using absorption the process by which soluble products oxygen of digestion move into the blood from the small intestine antibacterial chemicals chemicals produced by plants as a defence mechanism; the amount abstinence method of contraception whereby the produced will increase if the plant is under attack couple refrains from intercourse, particularly when an egg might be in the oviduct antibiotic e.g. penicillin; medicines that work inside the body to kill bacterial pathogens accommodation ability of the eyes to change focus antibody protein normally present in the body acid rain rain water which is made more acidic by or produced in response to an antigen, which it pollutant gases neutralises, thus producing an immune response active site the place on an enzyme where the antimicrobial resistance (AMR) an increasing substrate molecule binds problem in the twenty-first century whereby active transport in active transport, cells use energy bacteria have evolved to develop resistance against to transport substances through cell membranes antibiotics due to their overuse against a concentration gradient antiretroviral drugs drugs used to treat HIV adaptation features that organisms have to help infections; they -
Floral Symmetry Affects Speciation Rates in Angiosperms Risa D
Received 25 July 2003 Accepted 13 November 2003 Published online 16 February 2004 Floral symmetry affects speciation rates in angiosperms Risa D. Sargent Department of Zoology, University of British Columbia, 6270 University Boulevard, Vancouver, British Columbia V6T 1Z4, Canada ([email protected]) Despite much recent activity in the field of pollination biology, the extent to which animal pollinators drive the formation of new angiosperm species remains unresolved. One problem has been identifying floral adaptations that promote reproductive isolation. The evolution of a bilaterally symmetrical corolla restricts the direction of approach and movement of pollinators on and between flowers. Restricting pollin- ators to approaching a flower from a single direction facilitates specific placement of pollen on the pollin- ator. When coupled with pollinator constancy, precise pollen placement can increase the probability that pollen grains reach a compatible stigma. This has the potential to generate reproductive isolation between species, because mutations that cause changes in the placement of pollen on the pollinator may decrease gene flow between incipient species. I predict that animal-pollinated lineages that possess bilaterally sym- metrical flowers should have higher speciation rates than lineages possessing radially symmetrical flowers. Using sister-group comparisons I demonstrate that bilaterally symmetric lineages tend to be more species rich than their radially symmetrical sister lineages. This study supports an important role for pollinator- mediated speciation and demonstrates that floral morphology plays a key role in angiosperm speciation. Keywords: reproductive isolation; pollination; sister group comparison; zygomorphy 1. INTRODUCTION The importance of pollinator-mediated selection in angiosperms is well supported by theory (Kiester et al. -
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 Role of Jelly Coats in Sperm-Egg Encounters, Fertilization Success, and Selection on Egg Size in Broadcast Spawners
vol. 157, no. 6 the american naturalist june 2001 The Role of Jelly Coats in Sperm-Egg Encounters, Fertilization Success, and Selection on Egg Size in Broadcast Spawners Gregory S. Farley* and Don R. Levitan† Department of Biological Science, Florida State University, 1996a, 1998b; Coma and Lasker 1997). The proposed mech- Tallahassee, Florida 32306-1100 anism generating this result is simply that larger egg targets are more likely to be struck by swimming sperm (Rothschild Submitted February 2, 2000; Accepted January 19, 2001 and Swann 1949, 1951; Vogel et al. 1982). This finding has generated the hypothesis that sperm availability can influ- ence the evolutionary trade-off between egg size and num- ber (Levitan 1993, 1996a, 1996b, 1998a, 1998b). However, abstract: Sperm limitation may be an important selective force the idea that fertilization kinetics might influence this trade- influencing gamete traits such as egg size. The relatively inexpensive off has been challenged because of the notion that extra- extracellular structures surrounding many marine invertebrate eggs might serve to enhance collision rates without the added cost of cellular structures or chemoattractants may increase sperm- increasing the egg cell. However, despite decades of research, the egg collisions yet may not represent as great a cost to effects of extracellular structures on fertilization have not been con- fecundity as the trade-off associated with increased egg size clusively documented. Here, using the sea urchin Lytechinus varie- (Podolsky and Strathmann 1996; Styan 1998). These con- gatus, we remove jelly coats from eggs, and we quantify sperm col- tradictory ideas have not been resolved because data de- lisions to eggs with jelly coats, eggs without jelly coats, and inert tailing the influence of extracellular materials on fertilization plastic beads. -
Reproduction in Fungi: Genetical and Physiological Aspects by CHARLES G
J. Genet., Vol. 73, Number 1, April 1994, pp. 55-56. (~) Printed in India. BOOK REVIEW Reproduction in Fungi: Genetical and Physiological Aspects By CHARLES G. ELLIOTT; Chapman & Hall, London, 1994; 310 pages; s 35.00 It is now ahnost one hundred years since Klebs (1986)laid the foundation of a scientific approach to the study of reproduction in fungi. Since then an extensive literature has accumulated on reproduction in fungi. To present this information ill terms of principles and concepts and to highlight the immediate problems for study is a daunting task. C. G. Elliott has made a commendable attempt in presenting an overview of the genetical and physiological aspects of fungal reproduction. Fungi are remarkable for producing many kinds of reproductive structures in many ways. They produce spores both asexually and sexually. A single fungus produces a single kind of sexual spore: oospores in phycomycetes, ascospores in ascmnycetes and basidiospores in basidiomycetes. The underlying genetical and physiological mechanisms in the formation of spores are complex and we are only beginning to discern them. The introductory chapter examines the advantages of both asexual and sexual reproduction and the persistence of sex in the face of the apparent advantage of asexual reproduction. The reader is reminded that sexual reproduction in fungi not only serves to generate variability, but also provides a means of repairing damaged DNA. Moreover, it can give rise to propagules resistant to unfavourable environmental conditions. In the chapters that follow, one learns that superimposed on the basic event of nuclear fusion are a variety of regulating medhanisms, the effects of which are to determine a successful mating. -
Fertilization Selection on Egg and Jelly-Coat Size in the Sand Dollar Dendraster Excentricus
Evolution, 55(12), 2001, pp. 2479±2483 FERTILIZATION SELECTION ON EGG AND JELLY-COAT SIZE IN THE SAND DOLLAR DENDRASTER EXCENTRICUS DON R. LEVITAN1,2 AND STACEY D. IRVINE2 1Department of Biological Science, Florida State University, Tallahassee, Florida 32306-1100 2Bam®eld Marine Station, Bam®eld, British Columbia VOR 1B0, Canada Abstract. Organisms with external fertilization are often sperm limited, and in echinoids, larger eggs have a higher probability of fertilization than smaller eggs. This difference is thought to be a result of the more frequent sperm- egg collisions experienced by larger targets. Here we report how two components of egg target size, the egg cell and jelly coat, contributed to fertilization success in a selection experiment. We used a cross-sectional analysis of correlated characters to estimate the selection gradients on egg and jelly-coat size in ®ve replicate male pairs of the sand dollar Dendraster excentricus. Results indicated that eggs with larger cells and jelly coats were preferentially fertilized under sperm limitation in the laboratory. The selection gradients were an average of 922% steeper for egg than for jelly- coat size. The standardized selection gradients for egg and jelly-coat size were similar. Our results suggest that fertilization selection can act on both egg-cell and jelly-coat size but that an increase in egg-cell volume is much more likely to increase fertilization success than an equal change in jelly-coat volume. The strengths of the selection gradients were inversely related to the correlation of egg traits across replicate egg clutches. This result suggests the importance of replication in studies of selection of correlated characters. -
Lesson 6: Plant Reproduction
LESSON 6: PLANT REPRODUCTION LEVEL ONE Like every living thing on earth, plants need to make more of themselves. Biological structures wear out over time and need to be replaced with new ones. We’ve already looked at how non-vascular plants reproduce (mosses and liverworts) so now it’s time to look at vascular plants. If you look back at the chart on page 17, you will see that vascular plants are divided into two main categories: plants that produce seeds and plants that don’t produce seeds. The vascular plants that do not make seeds are basically the ferns. There are a few other smaller categories such as “horse tails” and club mosses, but if you just remember the ferns, that’s fine. So let’s take a look at how ferns make more ferns. The leaves of ferns are called fronds, and brand new leaves that have not yet totally uncoiled are called fiddleheads because they look like the scroll-shaped end of a violin. Technically, the entire frond is a leaf. What looks like a stem is actually the fern’s equivalent of a petiole. (Botanists call it a stipe.) The stem of a fern plant runs under the ground and is called a rhizome. Ferns also have roots, like all other vascular plants. The roots grow out from the bottom of the rhizome. Ferns produce spores, just like mosses do. At certain times of the year, the backside of some fern fronds will be covered with little dots called sori. Sori is the plural form, meaning more than one of them. -
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 -
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.