Example of a Seedless Vascular Plant
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Gymnosperms the MESOZOIC: ERA of GYMNOSPERM DOMINANCE
Chapter 24 Gymnosperms THE MESOZOIC: ERA OF GYMNOSPERM DOMINANCE THE VASCULAR SYSTEM OF GYMNOSPERMS CYCADS GINKGO CONIFERS Pinaceae Include the Pines, Firs, and Spruces Cupressaceae Include the Junipers, Cypresses, and Redwoods Taxaceae Include the Yews, but Plum Yews Belong to Cephalotaxaceae Podocarpaceae and Araucariaceae Are Largely Southern Hemisphere Conifers THE LIFE CYCLE OF PINUS, A REPRESENTATIVE GYMNOSPERM Pollen and Ovules Are Produced in Different Kinds of Structures Pollination Replaces the Need for Free Water Fertilization Leads to Seed Formation GNETOPHYTES GYMNOSPERMS: SEEDS, POLLEN, AND WOOD THE ECOLOGICAL AND ECONOMIC IMPORTANCE OF GYMNOSPERMS The Origin of Seeds, Pollen, and Wood Seeds and Pollen Are Key Reproductive SUMMARY Innovations for Life on Land Seed Plants Have Distinctive Vegetative PLANTS, PEOPLE, AND THE Features ENVIRONMENT: The California Coast Relationships among Gymnosperms Redwood Forest 1 KEY CONCEPTS 1. The evolution of seeds, pollen, and wood freed plants from the need for water during reproduction, allowed for more effective dispersal of sperm, increased parental investment in the next generation and allowed for greater size and strength. 2. Seed plants originated in the Devonian period from a group called the progymnosperms, which possessed wood and heterospory, but reproduced by releasing spores. Currently, five lineages of seed plants survive--the flowering plants plus four groups of gymnosperms: cycads, Ginkgo, conifers, and gnetophytes. Conifers are the best known and most economically important group, including pines, firs, spruces, hemlocks, redwoods, cedars, cypress, yews, and several Southern Hemisphere genera. 3. The pine life cycle is heterosporous. Pollen strobili are small and seasonal. Each sporophyll has two microsporangia, in which microspores are formed and divide into immature male gametophytes while still retained in the microsporangia. -
"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
The Big Bloom—How Flowering Plants Changed the World
The Big Bloom—How Flowering Plants Changed the World Written by Michael Klesius Republished from the pages of National Geographic magazine -- July 2002 In the summer of 1973 sunflowers appeared in my father's vegetable garden. They seemed to sprout overnight in a few rows he had lent that year to new neighbors from California. Only six years old at the time, I was at first put off by these garish plants. Such strange and vibrant flowers seemed out of place among the respectable beans, peppers, spinach, and other vegetables we had always grown. Gradually, however, the brilliance of the sunflowers won me over. Their fiery halos relieved the green monotone that by late summer ruled the garden. I marveled at birds that clung upside down to the shaggy, gold disks, wings fluttering, looting the seeds. Sunflowers defined flowers for me that summer and changed my view of the world. Flowers have a way of doing that. They began changing the way the world looked almost as soon as they appeared on Earth about 130 million years ago, during the Cretaceous period. That's relatively recent in geologic time: If all Earth's history were compressed into an hour, flowering plants would exist for only the last 90 seconds. But once they took firm root about 100 million years ago, they swiftly diversified in an explosion of varieties that established most of the flowering plant families of the modern world. Today flowering plant species outnumber by twenty to one those of ferns and cone-bearing trees, or conifers, which had thrived for 200 million years before the first bloom appeared. -
Ordovician Land Plants and Fungi from Douglas Dam, Tennessee
PROOF The Palaeobotanist 68(2019): 1–33 The Palaeobotanist 68(2019): xxx–xxx 0031–0174/2019 0031–0174/2019 Ordovician land plants and fungi from Douglas Dam, Tennessee GREGORY J. RETALLACK Department of Earth Sciences, University of Oregon, Eugene, OR 97403, USA. *Email: gregr@uoregon. edu (Received 09 September, 2019; revised version accepted 15 December, 2019) ABSTRACT The Palaeobotanist 68(1–2): Retallack GJ 2019. Ordovician land plants and fungi from Douglas Dam, Tennessee. The Palaeobotanist 68(1–2): xxx–xxx. 1–33. Ordovician land plants have long been suspected from indirect evidence of fossil spores, plant fragments, carbon isotopic studies, and paleosols, but now can be visualized from plant compressions in a Middle Ordovician (Darriwilian or 460 Ma) sinkhole at Douglas Dam, Tennessee, U. S. A. Five bryophyte clades and two fungal clades are represented: hornwort (Casterlorum crispum, new form genus and species), liverwort (Cestites mirabilis Caster & Brooks), balloonwort (Janegraya sibylla, new form genus and species), peat moss (Dollyphyton boucotii, new form genus and species), harsh moss (Edwardsiphyton ovatum, new form genus and species), endomycorrhiza (Palaeoglomus strotheri, new species) and lichen (Prototaxites honeggeri, new species). The Douglas Dam Lagerstätte is a benchmark assemblage of early plants and fungi on land. Ordovician plant diversity now supports the idea that life on land had increased terrestrial weathering to induce the Great Ordovician Biodiversification Event in the sea and latest Ordovician (Hirnantian) -
Plant Classification
Plant Classification Vascular plants are a group that has a system Non-Vascular plants are low growing plants of tubes (roots, stems and leaves) to help that get materials directly from their them transport materials throughout the surroundings. They have small root-like plant. Tubes called xylem move water from structures called rhizoids which help them the roots to the stems and leaves. Tubes adhere to their substrate. They undergo called phloem move food from the leaves asexual reproduction through vegetative (where sugar is made during propagation and sexual reproduction using photosynthesis) to the rest of the plant’s spores. Examples include bryophytes like cells. Vascular plants reproduce asexually hornworts, liverworts, and mosses. through spores and vegetative propagation (small part of the plant breaks off and forms a new plant) and sexually through pollen (sperm) and ovules (eggs). A gymnosperm is a vascular plant whose An angiosperm is a vascular plant whose seeds are not enclosed in an ovule or fruit. mature seeds are enclosed in a fruit or The name means “naked seed” and the ovule. They are flowering plants that group typically refers to conifers that bear reproduce using seeds and are either male and female cones, have needle-like “perfect” and contain both male and female leaves and are evergreen (leaves stay green reproductive structures or “imperfect” and year round and do not drop their leaves contain only male or female structures. during the fall and winter. Examples include Angiosperm trees are also called hardwoods pine trees, ginkgos and cycads. and they have broad leaves that change color and drop during the fall and winter. -
Biodiversity and Evolution in the Vanilla Genus
1 Biodiversity and Evolution in the Vanilla Genus Gigant Rodolphe1,2, Bory Séverine1,2, Grisoni Michel2 and Besse Pascale1 1University of La Reunion, UMR PVBMT 2CIRAD, UMR PVBMT, France 1. Introduction Since the publication of the first vanilla book by Bouriquet (1954c) and the more recent review on vanilla biodiversity (Bory et al., 2008b), there has been a world regain of interest for this genus, as witnessed by the recently published vanilla books (Cameron, 2011a; Havkin-Frenkel & Belanger, 2011; Odoux & Grisoni, 2010). A large amount of new data regarding the genus biodiversity and its evolution has also been obtained. These will be reviewed in the present paper and new data will also be presented. 2. Biogeography, taxonomy and phylogeny 2.1 Distribution and phylogeography Vanilla Plum. ex Miller is an ancient genus in the Orchidaceae family, Vanilloideae sub- family, Vanilleae tribe and Vanillinae sub-tribe (Cameron, 2004, 2005). Vanilla species are distributed throughout the tropics between the 27th north and south parallels, but are absent in Australia. The genus is most diverse in tropical America (52 species), and can also be found in Africa (14 species) and the Indian ocean islands (10 species), South-East Asia and New Guinea (31 species) and Pacific islands (3 species) (Portères, 1954). From floral morphological observations, Portères (1954) suggested a primary diversification centre of the Vanilla genus in Indo-Malaysia, followed by dispersion on one hand from Asia to Pacific and then America, and on the other hand from Madagascar to Africa. This hypothesis was rejected following the first phylogenetic studies of the genus (Cameron, 1999, 2000) which suggested a different scenario with an American origin of the genus (160 to 120 Mya) and a transcontinental migration of the Vanilla genus before the break-up of Gondwana (Cameron, 2000, 2003, 2005; Cameron et al., 1999). -
The Origin of Alternation of Generations in Land Plants
Theoriginof alternation of generations inlandplants: afocuson matrotrophy andhexose transport Linda K.E.Graham and LeeW .Wilcox Department of Botany,University of Wisconsin, 430Lincoln Drive, Madison,WI 53706, USA (lkgraham@facsta¡.wisc .edu ) Alifehistory involving alternation of two developmentally associated, multicellular generations (sporophyteand gametophyte) is anautapomorphy of embryophytes (bryophytes + vascularplants) . Microfossil dataindicate that Mid ^Late Ordovicianland plants possessed such alifecycle, and that the originof alternationof generationspreceded this date.Molecular phylogenetic data unambiguously relate charophyceangreen algae to the ancestryof monophyletic embryophytes, and identify bryophytes as early-divergentland plants. Comparison of reproduction in charophyceans and bryophytes suggests that the followingstages occurredduring evolutionary origin of embryophytic alternation of generations: (i) originof oogamy;(ii) retention ofeggsand zygotes on the parentalthallus; (iii) originof matrotrophy (regulatedtransfer ofnutritional and morphogenetic solutes fromparental cells tothe nextgeneration); (iv)origin of a multicellularsporophyte generation ;and(v) origin of non-£ agellate, walled spores. Oogamy,egg/zygoteretention andmatrotrophy characterize at least some moderncharophyceans, and arepostulated to represent pre-adaptativefeatures inherited byembryophytes from ancestral charophyceans.Matrotrophy is hypothesizedto have preceded originof the multicellularsporophytes of plants,and to represent acritical innovation.Molecular -
Seedless Plants Key Concept Seedless Plants Do Not Produce Seeds 2 but Are Well Adapted for Reproduction and Survival
Seedless Plants Key Concept Seedless plants do not produce seeds 2 but are well adapted for reproduction and survival. What You Will Learn When you think of plants, you probably think of plants, • Nonvascular plants do not have such as trees and flowers, that make seeds. But two groups of specialized vascular tissues. plants don’t make seeds. The two groups of seedless plants are • Seedless vascular plants have specialized vascular tissues. nonvascular plants and seedless vascular plants. • Seedless plants reproduce sexually and asexually, but they need water Nonvascular Plants to reproduce. Mosses, liverworts, and hornworts do not have vascular • Seedless plants have two stages tissue to transport water and nutrients. Each cell of the plant in their life cycle. must get water from the environment or from a nearby cell. So, Why It Matters nonvascular plants usually live in places that are damp. Also, Seedless plants play many roles in nonvascular plants are small. They grow on soil, the bark of the environment, including helping to form soil and preventing erosion. trees, and rocks. Mosses, liverworts, and hornworts don’t have true stems, roots, or leaves. They do, however, have structures Vocabulary that carry out the activities of stems, roots, and leaves. • rhizoid • rhizome Mosses Large groups of mosses cover soil or rocks with a mat of Graphic Organizer In your Science tiny green plants. Mosses have leafy stalks and rhizoids. A Journal, create a Venn Diagram that rhizoid is a rootlike structure that holds nonvascular plants in compares vascular plants and nonvas- place. Rhizoids help the plants get water and nutrients. -
PHASEOLUS LESSON ONE PHASEOLUS and the FABACEAE INTRODUCTION to the FABACEAE
1 PHASEOLUS LESSON ONE PHASEOLUS and the FABACEAE In this lesson we will begin our study of the GENUS Phaseolus, a member of the Fabaceae family. The Fabaceae are also known as the Legume Family. We will learn about this family, the Fabaceae and some of the other LEGUMES. When we study about the GENUS and family a plant belongs to, we are studying its TAXONOMY. For this lesson to be complete you must: ___________ do everything in bold print; ___________ answer the questions at the end of the lesson; ___________ complete the world map at the end of the lesson; ___________ complete the table at the end of the lesson; ___________ learn to identify the different members of the Fabaceae (use the study materials at www.geauga4h.org); and ___________ complete one of the projects at the end of the lesson. Parts of the lesson are in underlined and/or in a different print. Younger members can ignore these parts. WORDS PRINTED IN ALL CAPITAL LETTERS may be new vocabulary words. For help, see the glossary at the end of the lesson. INTRODUCTION TO THE FABACEAE The genus Phaseolus is part of the Fabaceae, or the Pea or Legume Family. This family is also known as the Leguminosae. TAXONOMISTS have different opinions on naming the family and how to treat the family. Members of the Fabaceae are HERBS, SHRUBS and TREES. Most of the members have alternate compound leaves. The FRUIT is usually a LEGUME, also called a pod. Members of the Fabaceae are often called LEGUMES. Legume crops like chickpeas, dry beans, dry peas, faba beans, lentils and lupine commonly have root nodules inhabited by beneficial bacteria called rhizobia. -
The Paleohistory of California Oaks1
1 The Paleohistory of California Oaks 2 Scott Mensing Abstract Oak woodlands are a fixture of California geography, yet as recently as 10,000 years ago oaks were only a minor element in the landscape. The first fossil evidence for California’s oaks is in the early Miocene (~20 million years ago) when oaks were present across the west, intermixed with deciduous trees typical of eastern North America. As climate became drier, species dependent upon summer precipitation went locally extinct and oaks retreated west of the Sierra Nevada. During the Pleistocene (the last 2 million years) oak abundance declined during cool glacial periods and expanded during warm interglacials. After the last glacial maximum (~18,000 years ago), oaks expanded rapidly to become the dominant trees in the Coast Ranges, Sierra Nevada foothills, and Peninsular Ranges. During the Holocene (the last 10,000 years) oaks in the Sierra Nevada were most abundant during a warm dry period between 8000 and 6000 years ago. Native American use of fire to manipulate plants for food, basketry, tools, and other uses helped maintain oak woodlands and reduce expansion of conifers where these forest types overlapped. Fire suppression, initiated by the Spanish and reinforced during the American period has allowed oak woodland density to increase in some areas in the Coast Range, but has decreased oaks where pines are dominant. Extensive cutting of oaks has reduced their populations throughout much of the state. Key words: California, oak woodlands, paleoecology, Quercus, vegetation history Introduction Oak woodlands characterize much of the California landscape, but widespread oak communities are of relatively recent origin in the state. -
Ecological Sorting of Vascular Plant Classes During the Paleozoic Evolutionary Radiation
i1 Ecological Sorting of Vascular Plant Classes During the Paleozoic Evolutionary Radiation William A. DiMichele, William E. Stein, and Richard M. Bateman DiMichele, W.A., Stein, W.E., and Bateman, R.M. 2001. Ecological sorting of vascular plant classes during the Paleozoic evolutionary radiation. In: W.D. Allmon and D.J. Bottjer, eds. Evolutionary Paleoecology: The Ecological Context of Macroevolutionary Change. Columbia University Press, New York. pp. 285-335 THE DISTINCTIVE BODY PLANS of vascular plants (lycopsids, ferns, sphenopsids, seed plants), corresponding roughly to traditional Linnean classes, originated in a radiation that began in the late Middle Devonian and ended in the Early Carboniferous. This relatively brief radiation followed a long period in the Silurian and Early Devonian during wrhich morphological complexity accrued slowly and preceded evolutionary diversifications con- fined within major body-plan themes during the Carboniferous. During the Middle Devonian-Early Carboniferous morphological radiation, the major class-level clades also became differentiated ecologically: Lycopsids were cen- tered in wetlands, seed plants in terra firma environments, sphenopsids in aggradational habitats, and ferns in disturbed environments. The strong con- gruence of phylogenetic pattern, morphological differentiation, and clade- level ecological distributions characterizes plant ecological and evolutionary dynamics throughout much of the late Paleozoic. In this study, we explore the phylogenetic relationships and realized ecomorphospace of reconstructed whole plants (or composite whole plants), representing each of the major body-plan clades, and examine the degree of overlap of these patterns with each other and with patterns of environmental distribution. We conclude that 285 286 EVOLUTIONARY PALEOECOLOGY ecological incumbency was a major factor circumscribing and channeling the course of early diversification events: events that profoundly affected the structure and composition of modern plant communities. -
Dermal Morphology of <Emphasis Type="Italic">Vanilla Planifolia
Proc. Indian Acad. Sci., Vol. 84 B, No. 5, 1976, pp. 173-179 Dermal morphology of Vanilla planifolia Andr. and V. wightii Lindl. B. K. NAYAR, F.A.Sc., RAJENDRA RAI AND P. VATSALA Department of Botany, Calicut University, Kerala 673635 MS received 8 April 1976 ABSTRACT In contrast to other Orchidaceae, the stomata in Va;ziila planifolia and V. wightii, are predominantly of the para-mesoperigenous type but the meristemoid is squarish as in other members of the family. 16~S of the stomata in V. planifclia and the stomata on the scale-leaves of V. wightii are of the aperigenous type; in V. planifolia, a few stomata (8~) are anisomesogenous (meristemoid triangular) and others (2~o) hemipara-mesop~rigenous. In V. Mghtii subsidiary cells of the para- mesoperigenous cauline stomata divide secondarily to form 5-7 subsidiary cells. Stomata are abundant on the stem of V. wightii (stomatal index-3.4) but sparse in V. planifolia (index-0.57). There is a progressive increase in stomatal index from base to apex of the leaf of V. planifolia. About 80~; of the the stomata in mature leaves of V. planifolia degenerate, as leaves get older.The epidermis is devoid of trichom~s in both species. In V. planifc.lia, each epidermal cell has a large crystal included in it. It is suggested that the stomatal types in Vanilla indicate the relationship of Orchidaceae to Hypoxidaceae, through Curculigo, which also has para- mesoperigenous stomata. 1. INTRODUCTION DIFFERENT Natural Orders, especially of the Monocotyledons, are reported to possess characteristic stomatal types and the aperigenous type is the rule in Orchidaceae.