Plant Diversity Plant Diversity
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Origin of Gibberellin-Dependent Transcriptional Regulation by Molecular Exploitation of a Transactivation Domain in DELLA Proteins
bioRxiv preprint doi: https://doi.org/10.1101/398883; this version posted December 10, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.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 4.0 International license. Article - Discoveries Origin of gibberellin-dependent transcriptional regulation by molecular exploitation of a transactivation domain in DELLA proteins Jorge Hernández-García1, Asier Briones-Moreno1, Renaud Dumas2, and Miguel A. Blázquez1 1Instituto de Biología Molecular y Celular de Plantas (IBMCP), CSIC-Universidad Politécnica de Valencia, Campus UPV CPI 8E, Valencia, Spain 2Laboratoire de Physiologie Cellulaire et Végétale, Université Grenoble Alpes, CNRS, Commissariat à l'Energie Atomique et aux Energies Alternatives/Biosciences and Biotechnology Institute of Grenoble, Institut National de la Recherche Agronomique (INRA), Grenoble, France Corresponding author: Miguel A. Blázquez ([email protected]) 1 bioRxiv preprint doi: https://doi.org/10.1101/398883; this version posted December 10, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.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 4.0 International license. Abstract DELLA proteins are land-plant specific transcriptional regulators known to interact through their C-terminal GRAS domain with over 150 transcription factors in Arabidopsis thaliana. Besides, DELLAs from vascular plants can interact through the N-terminal domain with the gibberellin receptor encoded by GID1, through which gibberellins promote DELLA degradation. However, this regulation is absent in non-vascular land plants, which lack active gibberellins or a proper GID1 receptor. -
BIOLOGY ASSIGNMENT CLASS IX UNIT II- FLOWERING PLANT Chap 3- the Flower
BIOLOGY ASSIGNMENT CLASS IX UNIT II- FLOWERING PLANT Chap 3- The Flower Flower is the most attractive,brightly coloured and significant part of plant. It help in sexual reproduction and later forms fruit and seeds. Characterstic of flower : The flower possesss the following characterstic – 1. Flower is the highly modified and specialized shoot meant for Sexual Reproduction. 2.The nodes and internodes are highly condensed to form a flat thalamus or receptacles. 3. Thalamus is quiet short and usually borne at the end of the stalk called Pedicel. 4.The flower arise from the leaf like structure called bract. 5. The floral part of flower are borne on thalamus in the form of four whorls. 6. These four whorl includes from outer side – Calyx ( sepal ), Corolla( petal ) , Androecium (stamen ), Gynoecium ( carpel ). Parts of a Flower : Floweris attached with the stem or its branch with the help of a stalk called Pedicel. If the flower is without pedicel it is called sessile . The pedicel arises from the axil of green leaf like structure called Bract.The other swollen end of the pedicel is Thalamus or torus . On the thalamus usually four whorl of Floral structure are present These four whorl from outside to inside are : i. Calyx iii. Androecium ii. Corolla iv. Gynoecium I. CALYX It is the outermost and the lowermost whorl , green in colour which cover an unopened bud .The single unit of Calyx is called sepal .It may be fussed or free from each other. Additional floral whorl outside the Calyx is called Epicalyx. Function of Calyx : i. -
Pollen Tube Guidance by Pistils Ensures Successful Double Fertilization Ravishankar Palanivelu∗ and Tatsuya Tsukamoto
Advanced Review Pathfinding in angiosperm reproduction: pollen tube guidance by pistils ensures successful double fertilization Ravishankar Palanivelu∗ and Tatsuya Tsukamoto Sexual reproduction in flowering plants is unique in multiple ways. Distinct multicellular gametophytes contain either a pair of immotile, haploid male gametes (sperm cells) or a pair of female gametes (haploid egg cell and homodiploid central cell). After pollination, the pollen tube, a cellular extension of the male gametophyte, transports both male gametes at its growing tip and delivers them to the female gametes to affect double fertilization. The pollen tube travels a long path and sustains its growth over a considerable amount of time in the female reproductive organ (pistil) before it reaches the ovule, which houses the female gametophyte. The pistil facilitates the pollen tube’s journey by providing multiple, stage-specific, nutritional, and guidance cues along its path. The pollen tube interacts with seven different pistil cell types prior to completing its journey. Consequently, the pollen tube has a dynamic gene expression program allowing it to continuously reset and be receptive to multiple pistil signals as it migrates through the pistil. Here, we review the studies, including several significant recent advances, that led to a better understanding of the multitude of cues generated by the pistil tissues to assist the pollen tube in delivering the sperm cells to the female gametophyte. We also highlight the outstanding questions, draw attention to opportunities created by recent advances and point to approaches that could be undertaken to unravel the molecular mechanisms underlying pollen tube–pistil interactions. 2011 Wiley Periodicals, Inc. -
Plant Evolution an Introduction to the History of Life
Plant Evolution An Introduction to the History of Life KARL J. NIKLAS The University of Chicago Press Chicago and London CONTENTS Preface vii Introduction 1 1 Origins and Early Events 29 2 The Invasion of Land and Air 93 3 Population Genetics, Adaptation, and Evolution 153 4 Development and Evolution 217 5 Speciation and Microevolution 271 6 Macroevolution 325 7 The Evolution of Multicellularity 377 8 Biophysics and Evolution 431 9 Ecology and Evolution 483 Glossary 537 Index 547 v Introduction The unpredictable and the predetermined unfold together to make everything the way it is. It’s how nature creates itself, on every scale, the snowflake and the snowstorm. — TOM STOPPARD, Arcadia, Act 1, Scene 4 (1993) Much has been written about evolution from the perspective of the history and biology of animals, but significantly less has been writ- ten about the evolutionary biology of plants. Zoocentricism in the biological literature is understandable to some extent because we are after all animals and not plants and because our self- interest is not entirely egotistical, since no biologist can deny the fact that animals have played significant and important roles as the actors on the stage of evolution come and go. The nearly romantic fascination with di- nosaurs and what caused their extinction is understandable, even though we should be equally fascinated with the monarchs of the Carboniferous, the tree lycopods and calamites, and with what caused their extinction (fig. 0.1). Yet, it must be understood that plants are as fascinating as animals, and that they are just as important to the study of biology in general and to understanding evolutionary theory in particular. -
Number of Living Species in Australia and the World
Numbers of Living Species in Australia and the World 2nd edition Arthur D. Chapman Australian Biodiversity Information Services australia’s nature Toowoomba, Australia there is more still to be discovered… Report for the Australian Biological Resources Study Canberra, Australia September 2009 CONTENTS Foreword 1 Insecta (insects) 23 Plants 43 Viruses 59 Arachnida Magnoliophyta (flowering plants) 43 Protoctista (mainly Introduction 2 (spiders, scorpions, etc) 26 Gymnosperms (Coniferophyta, Protozoa—others included Executive Summary 6 Pycnogonida (sea spiders) 28 Cycadophyta, Gnetophyta under fungi, algae, Myriapoda and Ginkgophyta) 45 Chromista, etc) 60 Detailed discussion by Group 12 (millipedes, centipedes) 29 Ferns and Allies 46 Chordates 13 Acknowledgements 63 Crustacea (crabs, lobsters, etc) 31 Bryophyta Mammalia (mammals) 13 Onychophora (velvet worms) 32 (mosses, liverworts, hornworts) 47 References 66 Aves (birds) 14 Hexapoda (proturans, springtails) 33 Plant Algae (including green Reptilia (reptiles) 15 Mollusca (molluscs, shellfish) 34 algae, red algae, glaucophytes) 49 Amphibia (frogs, etc) 16 Annelida (segmented worms) 35 Fungi 51 Pisces (fishes including Nematoda Fungi (excluding taxa Chondrichthyes and (nematodes, roundworms) 36 treated under Chromista Osteichthyes) 17 and Protoctista) 51 Acanthocephala Agnatha (hagfish, (thorny-headed worms) 37 Lichen-forming fungi 53 lampreys, slime eels) 18 Platyhelminthes (flat worms) 38 Others 54 Cephalochordata (lancelets) 19 Cnidaria (jellyfish, Prokaryota (Bacteria Tunicata or Urochordata sea anenomes, corals) 39 [Monera] of previous report) 54 (sea squirts, doliolids, salps) 20 Porifera (sponges) 40 Cyanophyta (Cyanobacteria) 55 Invertebrates 21 Other Invertebrates 41 Chromista (including some Hemichordata (hemichordates) 21 species previously included Echinodermata (starfish, under either algae or fungi) 56 sea cucumbers, etc) 22 FOREWORD In Australia and around the world, biodiversity is under huge Harnessing core science and knowledge bases, like and growing pressure. -
Ap09 Biology Form B Q2
AP® BIOLOGY 2009 SCORING GUIDELINES (Form B) Question 2 Discuss the patterns of sexual reproduction in plants. Compare and contrast reproduction in nonvascular plants with that in flowering plants. Include the following topics in your discussion: (a) alternation of generations (b) mechanisms that bring female and male gametes together (c) mechanisms that disperse offspring to new locations Four points per part. Student must write about all three parts for full credit. Within each part it is possible to get points for comparing and contrasting. Also, specific points are available from details provided about nonvascular and flowering plants. Discuss the patterns of sexual reproduction in plants (4 points maximum): (a) Alternation of generations (4 points maximum): Topic Description (1 point each) Alternating generations Haploid stage and diploid stage. Gametophyte Haploid-producing gametes. Dominant in nonvascular plants. Double fertilization in flowering plants. Gametangia; archegonia and antheridia in nonvascular plants. Sporophyte Diploid-producing spores. Heterosporous in flowering plants. Flowering plants produce seeds; nonvascular plants do not. Flowering plants produce flower structures. Sporangia (megasporangia and microsporangia). Dominant in flowering plants. (b) Mechanisms that bring female and male gametes together (4 points maximum): Nonvascular Plants (1 point each) Flowering Plants (1 point each) Aquatic—requires water for motile sperm Terrestrial—pollination by wind, water, or animal Micropyle in ovule for pollen tube to enter Pollen tube to carry sperm nuclei Self- or cross-pollination Antheridia produce sperm Gametophytes; no antheridia or archegonia Archegonia produce egg Ovules produce female gametophytes/gametes Pollen: male gametophyte that produces gametes © 2009 The College Board. All rights reserved. Visit the College Board on the Web: www.collegeboard.com. -
Chlorophyta Is a Division of Green Algae, Informally Called
Chlorophyta is a division of green algae, informally waters of the Sargasso Sea. Many brown algae, such as called chlorophytes. The name is used in two very members of the order Fucales, commonly grow along different senses so that care is needed to determine the rocky seashores. Some members of the class are used as use by a particular author. In older classification food for humans. systems, it refers to a highly paraphyletic group of all Worldwide there are about 1500–2000 species of brown the green algae within the green plants (Viridiplantae), algae.[4] Some species are of sufficient commercial and thus includes about 7,000 species [4] [5] of mostly importance, such as Ascophyllum nodosum , that they aquatic photosynthetic eukaryotic organisms. Like the have become subjects of extensive research in their own land plants (bryophytes and tracheophytes), green algae right.[5] [4] contain chlorophylls a and b, and store food as starch Brown algae belong to a very large group, the in their plastids. Heterokontophyta, a eukaryotic group of organisms In newer classifications, it refers to one of the two distinguished most prominently by having chloroplasts clades making up the Viridiplantae, which are the surrounded by four membranes, suggesting an origin chlorophytes and the streptophytes or charophytes.[6][7] from a symbiotic relationship between a basal In this sense it includes only about 4,300 species.[3] eukaryote and another eukaryotic organism. Most brown algae contain the pigment fucoxanthin, which is responsible for the distinctive greenish-brown color that The red algae, or Rhodophyta ( / r o ʊ ˈ d ɒ f ɨ t ə / or / gives them their name. -
Functional Analyses of Genetic Pathways Controlling Petal Specification in Poppy Sinéad Drea1, Lena C
RESEARCH ARTICLE 4157 Development 134, 4157-4166 (2007) doi:10.1242/dev.013136 Functional analyses of genetic pathways controlling petal specification in poppy Sinéad Drea1, Lena C. Hileman1,*, Gemma de Martino1 and Vivian F. Irish1,2,† MADS-box genes are crucial regulators of floral development, yet how their functions have evolved to control different aspects of floral patterning is unclear. To understand the extent to which MADS-box gene functions are conserved or have diversified in different angiosperm lineages, we have exploited the capability for functional analyses in a new model system, Papaver somniferum (opium poppy). P. somniferum is a member of the order Ranunculales, and so represents a clade that is evolutionarily distant from those containing traditional model systems such as Arabidopsis, Petunia, maize or rice. We have identified and characterized the roles of several candidate MADS-box genes in petal specification in poppy. In Arabidopsis, the APETALA3 (AP3) MADS-box gene is required for both petal and stamen identity specification. By contrast, we show that the AP3 lineage has undergone gene duplication and subfunctionalization in poppy, with one gene copy required for petal development and the other responsible for stamen development. These differences in gene function are due to differences both in expression patterns and co- factor interactions. Furthermore, the genetic hierarchy controlling petal development in poppy has diverged as compared with that of Arabidopsis. As these are the first functional analyses of AP3 genes in this evolutionarily divergent clade, our results provide new information on the similarities and differences in petal developmental programs across angiosperms. Based on these observations, we discuss a model for how the petal developmental program has evolved. -
Chapter 23: the Early Tracheophytes
Chapter 23 The Early Tracheophytes THE LYCOPHYTES Lycopodium Has a Homosporous Life Cycle Selaginella Has a Heterosporous Life Cycle Heterospory Allows for Greater Parental Investment Isoetes May Be the Only Living Member of the Lepidodendrid Group THE MONILOPHYTES Whisk Ferns Ophioglossalean Ferns Horsetails Marattialean Ferns True Ferns True Fern Sporophytes Typically Have Underground Stems Sexual Reproduction Usually Is Homosporous Fern Have a Variety of Alternative Means of Reproduction Ferns Have Ecological and Economic Importance SUMMARY PLANTS, PEOPLE, AND THE ENVIRONMENT: Sporophyte Prominence and Survival on Land PLANTS, PEOPLE, AND THE ENVIRONMENT: Coal, Smog, and Forest Decline THE OCCUPATION OF THE LAND PLANTS, PEOPLE, AND THE The First Tracheophytes Were ENVIRONMENT: Diversity Among the Ferns Rhyniophytes Tracheophytes Became Increasingly Better PLANTS, PEOPLE, AND THE Adapted to the Terrestrial Environment ENVIRONMENT: Fern Spores Relationships among Early Tracheophytes 1 KEY CONCEPTS 1. Tracheophytes, also called vascular plants, possess lignified water-conducting tissue (xylem). Approximately 14,000 species of tracheophytes reproduce by releasing spores and do not make seeds. These are sometimes called seedless vascular plants. Tracheophytes differ from bryophytes in possessing branched sporophytes that are dominant in the life cycle. These sporophytes are more tolerant of life on dry land than those of bryophytes because water movement is controlled by strongly lignified vascular tissue, stomata, and an extensive cuticle. The gametophytes, however still require a seasonally wet habitat, and water outside the plant is essential for the movement of sperm from antheridia to archegonia. 2. The rhyniophytes were the first tracheophytes. They consisted of dichotomously branching axes, lacking roots and leaves. They are all extinct. -
Mitochondrial Genomes of the Early Land Plant Lineage
Dong et al. BMC Genomics (2019) 20:953 https://doi.org/10.1186/s12864-019-6365-y RESEARCH ARTICLE Open Access Mitochondrial genomes of the early land plant lineage liverworts (Marchantiophyta): conserved genome structure, and ongoing low frequency recombination Shanshan Dong1,2, Chaoxian Zhao1,3, Shouzhou Zhang1, Li Zhang1, Hong Wu2, Huan Liu4, Ruiliang Zhu3, Yu Jia5, Bernard Goffinet6 and Yang Liu1,4* Abstract Background: In contrast to the highly labile mitochondrial (mt) genomes of vascular plants, the architecture and composition of mt genomes within the main lineages of bryophytes appear stable and invariant. The available mt genomes of 18 liverwort accessions representing nine genera and five orders are syntenous except for Gymnomitrion concinnatum whose genome is characterized by two rearrangements. Here, we expanded the number of assembled liverwort mt genomes to 47, broadening the sampling to 31 genera and 10 orders spanning much of the phylogenetic breadth of liverworts to further test whether the evolution of the liverwort mitogenome is overall static. Results: Liverwort mt genomes range in size from 147 Kb in Jungermanniales (clade B) to 185 Kb in Marchantiopsida, mainly due to the size variation of intergenic spacers and number of introns. All newly assembled liverwort mt genomes hold a conserved set of genes, but vary considerably in their intron content. The loss of introns in liverwort mt genomes might be explained by localized retroprocessing events. Liverwort mt genomes are strictly syntenous in genome structure with no structural variant detected in our newly assembled mt genomes. However, by screening the paired-end reads, we do find rare cases of recombination, which means multiple concurrent genome structures may exist in the vegetative tissues of liverworts. -
Ecophysiology of Four Co-Occurring Lycophyte Species: an Investigation of Functional Convergence
Research Article Ecophysiology of four co-occurring lycophyte species: an investigation of functional convergence Jacqlynn Zier, Bryce Belanger, Genevieve Trahan and James E. Watkins* Department of Biology, Colgate University, Hamilton, NY 13346, USA Received: 22 June 2015; Accepted: 7 November 2015; Published: 24 November 2015 Associate Editor: Tim J. Brodribb Citation: Zier J, Belanger B, Trahan G, Watkins JE. 2015. Ecophysiology of four co-occurring lycophyte species: an investigation of functional convergence. AoB PLANTS 7: plv137; doi:10.1093/aobpla/plv137 Abstract. Lycophytes are the most early divergent extant lineage of vascular land plants. The group has a broad global distribution ranging from tundra to tropical forests and can make up an important component of temperate northeast US forests. We know very little about the in situ ecophysiology of this group and apparently no study has eval- uated if lycophytes conform to functional patterns expected by the leaf economics spectrum hypothesis. To determine factors influencing photosynthetic capacity (Amax), we analysed several physiological traits related to photosynthesis to include stomatal, nutrient, vascular traits, and patterns of biomass distribution in four coexisting temperate lycophyte species: Lycopodium clavatum, Spinulum annotinum, Diphasiastrum digitatum and Dendrolycopodium dendroi- deum. We found no difference in maximum photosynthetic rates across species, yet wide variation in other traits. We also found that Amax was not related to leaf nitrogen concentration and is more tied to stomatal conductance, suggestive of a fundamentally different sets of constraints on photosynthesis in these lycophyte taxa compared with ferns and seed plants. These findings complement the hydropassive model of stomatal control in lycophytes and may reflect canaliza- tion of function in this group. -
Seed Fertilization, Development, and Germination in Hydatellaceae (Nymphaeales): Implications for Endosperm Evolution in Early A
American Journal of Botany 96(9): 1581–1593. 2009. S EED FERTILIZATION, DEVELOPMENT, AND GERMINATION IN HYDATELLACEAE (NYMPHAEALES): IMPLICATIONS FOR ENDOSPERM EVOLUTION IN EARLY ANGIOSPERMS 1 Paula J. Rudall, 2,6 Tilly Eldridge, 2 Julia Tratt, 2 Margaret M. Ramsay, 2 Renee E. Tuckett, 3 Selena Y. Smith, 4,7 Margaret E. Collinson, 4 Margarita V. Remizowa, 5 and Dmitry D. Sokoloff 5 2 Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, UK; 3 The University of Western Australia, Crawley, WA 6009, Australia; 4 Department of Earth Sciences, Royal Holloway University of London, Egham, Surrey, TW20 0EX, UK; and 5 Department of Higher Plants, Biological Faculty, Moscow State University 119991, Moscow, Russia New data on endosperm development in the early-divergent angiosperm Trithuria (Hydatellaceae) indicate that double fertiliza- tion results in formation of cellularized micropylar and unicellular chalazal domains with contrasting ontogenetic trajectories, as in waterlilies. The micropylar domain ultimately forms the cellular endosperm in the dispersed seed. The chalazal domain forms a single-celled haustorium with a large nucleus; this haustorium ultimately degenerates to form a space in the dispersed seed, simi- lar to the chalazal endosperm haustorium of waterlilies. The endosperm condition in Trithuria and waterlilies resembles the helo- bial condition that characterizes some monocots, but contrasts with Amborella and Illicium , in which most of the mature endosperm is formed from the chalazal domain. The precise location of the primary endosperm nucleus governs the relative sizes of the cha- lazal and micropylar domains, but not their subsequent developmental trajectories. The unusual tissue layer surrounding the bi- lobed cotyledonary sheath in seedlings of some species of Trithuria is a belt of persistent endosperm, comparable with that of some other early-divergent angiosperms with a well-developed perisperm, such as Saururaceae and Piperaceae.