Trillium Seed Propagation William Cullina
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Seed Dispersal by Ants in Jarrah Forest Restorations of Western Australia
Seed Dispersal by Ants in Jarrah Forest Restorations of Western Australia Troy L. Wanless Introduction The jarrah forests in Western Australia cover approximately 1.75 million ha in the southwestern corner of the state (Figure 1). Jarrah, otherwise known as Eucalyptus marginata, is only one species among many that inhabit a region with considerable physical and biological diversity. 1200 species of plants, 29 mammalian species, 45 reptile species, 17 frog species, 4 fish species and 150 bird species live in this system which also has highly adverse conditions for survival. These may include infertile, often salt-laden soils, drought, and the occasional wildfire (Western Australia Forest Alliance, 2003). Considerable deposits of bauxite, which is the primary material involved in the production of aluminum, are scattered throughout the region. Since 1963, Alcoa of Australia Ltd. has cleared these jarrah forests to make way for mining of this ore. It is estimated that these deposits cover 7-8% of the forested area although only 3-4% will ever be mined due to environmental and economic constraints (Majer, 1989). These mined areas create a scattering of patches throughout the forest that are essentially stripped of any kind of biodiversity that was once there (Figure 2). Restoration efforts on these previously mined patches focus on many aspects of the jarrah forest ecosystem. Specifically interesting is the role that ants play in seed dispersal. This paper will focus on the topic of seed dispersal by ants in the northern jarrah forests of Western Australia while paying particular attention to myrmecochory. Figure 1. Location of jarrah forest in Australia Figure 2. -
Large-Flowered Trilliums Coming up in Spring in Our Childhoo
Large-flowered Trillium or Common Trillium (Trillium grandiflorum) Large-flowered Trilliums Coming Up in Spring In our childhood the woods in late May were full of hundreds of large, waxy white flowers that covered the forest floor. Grandma in her German diary called these trilliums “wild lilies” and also commented that on May14th and 22nd in 1927 and again on May 22nd in 1940 these flowers were numerous and in full bloom. (Freckman, 1994) gave the earliest blooming dates as April 24th. Large-flowered Trillium Bud Opening Today, with more houses and lawns in the country, and fewer undisturbed woodlots those visions of white are less frequently seen. In addition, the White-tailed Deer population has steadily increased and their appetite for tasty trilliums has served to eliminate many stands of this beautiful plant. This is especially troublesome because once the leaves and flowers are plucked, the plant is likely to die. It can no longer produce food to send down to the roots so that it can come back another year. It still grows quite abundantly on the sloping bank along Billings Avenue in the Town of Medford, Wisconsin. Some sources say that deer do not like to graze on steep banks or inclines so that may be why those plants have escaped. We have a patch of trilliums that has grown larger each year in our lawn. Recently we have had to protect these trilliums from the deer that could wipe out the entire patch in a single night. Sometimes seeds from those plants, possibly transported by ants, have grown into new plants in the front lawn. -
Patterns in Evolution in Characters That Define Iris Subgenera And
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 34 2006 Patterns in Evolution in Characters That Define rI is Subgenera and Sections Carol A. Wilson Rancho Santa Ana Botanic Garden Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Wilson, Carol A. (2006) "Patterns in Evolution in Characters That Define rI is Subgenera and Sections," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 34. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/34 Aliso 22, pp. 425-433 © 2006, Rancho Santa Ana Botanic Garden PATTERNS OF EVOLUTION IN CHARACTERS THAT DEFINE IRIS SUBGENERA AND SECTIONS CAROL A. WILSON Rancho Santa Ana Botanic Garden, 1500 North College Avenue, Claremont, California 91711-3157, USA (carol. wilson@ cgu. edu) ABSTRACT Subgeneric groups have been circumscribed in Iris based on a small number of morphological characters. Recent DNA sequence data has indicated that several of the subgenera, sections, and series that have previously been delineated are paraphyletic or polyphyletic. The evolution of characters that have traditionally been used to distinguish sub generic and sectional groups within Iris was investigated by mapping these characters on a phylogenetic tree based on matK sequence data. Results indicate that rhizomes are pleisomorphic for the genus and that three bulb types have arisen independently. My analysis shows that sepal beards, sepal crests, and seed arils show extensive homoplasy. Most of the homoplasy seen is associated with the circumscription of polyphyletic subgeneric groups such as the beardless subgenus Limniris. Some additional homoplasy is due to diversity within supported clades or the historical use of a single character in circumscribing more than one subgeneric group. -
Ants, Plants, and Seed Dispersal Ignorance: How Do Ants Enhance Persistence?
Ants, Plants, and Seed Dispersal Ignorance: How do Ants Enhance Persistence? Charles Kwit, Assistant Professor, Department of Forestry, Wildlife and Fisheries [email protected] Wednesday, 11 September 2013 12:20 PM, 160 Plant Biotech Building 1 Acknowledgements 2 References Albrecht and McCarthy (2011), Plant Ecology 212: 1465-1477 Berg-Binder and Suarez (2012), Oecologia 169: 763-772 Bond (2001), American Journal of Botany 88: 234-241 Canner et al. (2012), Acta Oecologica 40: 31-39 Christian & Stanton (2004), Ecology 85: 1101-1110 Culver & Beattie (1978), Journal of Ecology 66: 53-72 Garrido et al. (2009), Acta Oecologica 35: 393-399 Gomez et al. (2003), Ecography 26: 532-538 Imbert (2006), Plant Species Biology 21: 109-117 Kwit et al. (2012), American Midland Naturalist 168: 9-17 Leal et al. (2007), Annals of Botany 99: 885-894 Lengyel et al. (2010), Perspectives in Plant Ecology, Evolution and Systematics 12: 43-55 Lobstein & Rockwood (1993), Virginia Journal of Science 44: 59-72 Lopez-Vila & Garcia-Fayos (2005), Acta Oecologica 28: 157-162 Manzaneda & Rey (2012), Ecography 35: 322-332 Martins et al. (2006), Sociobiology 47: 265-274 Ness et al. (2009), Oikos 118: 1793-1804 Ohkawara (2005), Plant Species Biology 20: 145-148 Passos & Ferriera (1996), Biotropica 28: 697-700 Rico-Gray & Oliveira (2007), The Ecology and Evolution of Ant-Plant Interactions Smith et al. (1989), Ecology 70: 1649-1656 Soriano et al. (2012), Plant Biosystems 146: 143-152 Whigham (2004), Annual Review of Ecology, Evolution and Systematics 35: 583-621 3 Outline ✤ Myrmecochory and ant-plant mutualism ✤ Ant “seed treatment” experiment ✤ New natural history information ✤ Ant “seed dispersal” experiment ✤ Future directions 4 Myrmecochory and ant-plant mutualism ✤ Seed dispersal by ants, aided by elaiosome ✤ Common phenomenon found in > 11,000 plant species (Lengyel et al. -
Dispersal of Non-Myrmecochorous Plants by a ‘‘Keystone Disperser’’ Ant in a Mediterranean Habitat Reveals Asymmetric Interdependence
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital.CSIC Dispersal of non-myrmecochorous plants by a ‘‘keystone disperser’’ ant in a Mediterranean habitat reveals asymmetric interdependence A´ . Barroso • F. Amor • X. Cerda´ • R. R. Boulay Abstract In contrast to other plant–animal mutualisms, A. italicum, but a negligible fraction of P. lentiscus seeds. seed dispersal interactions, and particularly seed dispersal We conclude that in contrast to the common view, dispersal by ants, are generally considered asymmetric, non-special- of non-myrmecochorous Mediterranean plants by ants ized relationships in which dispersers depend less on plants might be an important phenomenon. Keystone disperser than vice versa. Although myrmecochory is well understood ants like A. senilis probably obtain an important fitness in many terrestrial ecosystems, dispersal of non-elaiosome- advantage from non-myrmecochorous diaspore collection. bearing seeds by ants has barely been studied outside the However, plant benefit may vary greatly according to the Neotropics. Aphaenogaster senilis, a common ant in amount of seeds per individual plant and the existence of Southern Spain, collects a great variety of non-myrmeco- alternative dispersal agents. chorous diaspores along with insect prey. At our study site, fleshy fruits of Arum italicum, Phillyrea angustifolia and Keywords Fleshy fruits Á Arum italicum Á Aphaenogaster Á Pistacia lentiscus represent up to one-fourth of the items Nutrition Á Dispersal collected by A. senilis from June to November. However, they are mostly ignored by other ants. In the laboratory, the addition of A. italicum fruits to A. senilis insect-based diet Introduction increased male production and both worker and queen pupae size. -
Rutgers Home Gardeners School: the Beauty of Bulbs
The Beauty of Bulbs Bruce Crawford March 17, 2018 Director, Rutgers Gardens Rutgersgardens.rutgers.edu In general, ‘bulbs’, or more properly, geophytes are easy plants to grow, requiring full sun, good drainage and moderately fertile soils. Geophytes are defined as any non-woody plant with an underground storage organ. These storage organs contain carbohydrates, nutrients and water and allow the plant to endure extended periods of time that are not suitable for plant growth. Types of Geophytes include: Bulb – Swollen leaves or leaf stalks, attached at the bottom to a modified stem called a basal plant. The outer layers are modified leaves called scales. Scales contain necessary foods to sustain the bulb during dormancy and early growth. The outermost scales become dry and form a papery covering or tunic. At the center are developed, albeit embryonic flowers, leaves and stem(s). Roots develop from the basal plate. Examples are Tulipia (Tulip), Narcissus (Daffodil), and Allium (Flowering Onion). Corm – A swollen stem that is modified for food storage. Eyes or growing points develop on top of the corm. Roots develop from a basal plate on the bottom of the corm, similar to bulbs. The dried bases of the leaves from an outer layer, also called the tunic. Examples include Crocus and Erythronium (Dog Tooth Violet). Tuber – Also a modified stem, but it lacks a basal plate and a tunic. Roots, shoots and leaves grow from eyes. Examples are Cyclamen, Eranthis (Winter Aconite) and Anemone (Wind Flower). Tuberous Roots – These enlarged storage elements resemble tubers but are swollen roots, not stems. During active growth, they produce a fibrous root system for water and nutrient absorption. -
Seed Dispersal Mutualisms Are Essential for the Survival of Diverse Plant Species and Communities Worldwide
ABSTRACT YOUNGSTEADT, ELSA KRISTEN. Neotropical Ant-Gardens: Behavioral and Chemical Ecology of an Obligate Ant-Plant Mutualism. (Under the direction of Coby Schal.) Seed dispersal mutualisms are essential for the survival of diverse plant species and communities worldwide. An outstanding but poorly understood ant-seed mutualism occurs in the Amazonian rainforest, where arboreal ants collect seeds of several taxonomically diverse plant species and cultivate them in nutrient-rich nests, forming abundant hanging gardens known as ant-gardens (AGs). AG ants and plants are dominant members of lowland Amazonian ecosystems, and their interaction is obligate and apparently species-specific. Though established AGs are limited to specific participants, it is unknown at what stage specificity arises. Seed fate pathways in AG epiphytes are undocumented, and the recognition cues that mediate the mutualism are unknown. Here the species specificity of the AG ant-seed interaction is assessed, and chemical cues are characterized that elicit seed- finding and seed-carrying in AG ants. To examine the specificity of the ant-seed interaction, general food baits and seeds of the AG plant Peperomia macrostachya were offered on alternate days at 108 bait stations. Seventy ant species were detected at food baits and could have interacted with AG seeds, but only three species collected P. macrostachya seeds, and 84% of observed seed removal by ants was attributed to C. femoratus. In a separate experiment, arthropod exclusion significantly reduced AG seed removal rates, but vertebrate exclusion did not. Thus species specific seed dispersal, rather than post-dispersal processes, appears to be the primary determinant of the distribution of AG plants. -
Guidebook to Invasive Nonnative Plants of the Elwha Watershed Restoration
Guidebook to Invasive Nonnative Plants of the Elwha Watershed Restoration Olympic National Park, Washington Cynthia Lee Riskin A project submitted in partial fulfillment of the requirements for the degree of Master of Environmental Horticulture University of Washington 2013 Committee: Linda Chalker-Scott Kern Ewing Sarah Reichard Joshua Chenoweth Program Authorized to Offer Degree: School of Environmental and Forest Sciences Guidebook to Invasive Nonnative Plants of the Elwha Watershed Restoration Olympic National Park, Washington Cynthia Lee Riskin Master of Environmental Horticulture candidate School of Environmental and Forest Sciences University of Washington, Seattle September 3, 2013 Contents Figures ................................................................................................................................................................. ii Tables ................................................................................................................................................................. vi Acknowledgements ....................................................................................................................................... vii Introduction ....................................................................................................................................................... 1 Bromus tectorum L. (BROTEC) ..................................................................................................................... 19 Cirsium arvense (L.) Scop. (CIRARV) -
Boydfrde2001.Pdf
American Journal of Botany 88(2): 234±241. 2001. ECOLOGICAL BENEFITS OF MYRMECOCHORY FOR THE ENDANGERED CHAPARRAL SHRUB FREMONTODENDRON DECUMBENS (STERCULIACEAE)1 ROBERT S. BOYD Department of Biological Sciences and Alabama Agricultural Experiment Station, Auburn University, Alabama 36849-5407 USA Fremontodendron decumbens grows in a single county in central California, USA. Prior research showed that its elaiosome-bearing seeds are dispersed by the harvester ant Messor andrei. I tested several hypotheses regarding the positive role of ant-mediated dispersal to F. decumbens: (1) Does ant-mediated seed dispersal facilitate seed escape from rodent predation?; (2) Does ant processing of seeds stimulate germination?; (3) Are ant middens more suitable microsites for seed or seedling survival in unburned chaparral areas?; and (4) Do survival bene®ts of dispersal occur post-®re in the form of differences in seedling survival probabilities and, if so, why? Results of tests of each hypothesis were: (1) similar percentages of seeds placed on ant middens and under F. decumbens shrub canopies were destroyed by rodents, but seeds from which elaiosomes had been removed were more likely to escape rodent predation; (2) seeds processed by ants did not germinate more readily than seeds removed directly from shrub branches; (3) seedling predation was a major cause of mortality in unburned chaparral on both ant middens and under shrubs, and overall seedling survival did not differ between the two microsites; (4) post-burn seedling survival was signi®cantly greater for seedlings dispersed away from F. decumbens shrub canopies, because dispersed seedlings were both less likely to be killed by predators and more likely to be growing in a gap created by the ®re-caused death of an established shrub. -
Boraginaceae: Boraginoideae)
Systematic Botany (2010), 35(2): pp. 409–419 © Copyright 2010 by the American Society of Plant Taxonomists Fossil and Extant Western Hemisphere Boragineae, and the Polyphyly of “Trigonotideae” Riedl (Boraginaceae: Boraginoideae) Maximilian Weigend , 1 , 4 Marc Gottschling , 2 Federico Selvi, 3 and Hartmut H. Hilger 1 1 Institut für Biologie – Systematische Botanik und Pflanzengeographie, Freie Universität Berlin, Altensteinstr. 6, D-14195 Berlin, Germany 2 Department Biologie, Systematische Botanik und Mykologie, Ludwig-Maximilians-Universität München, Munich, Germany 3 Dipartimento di Biologia Vegetale dell’Università, Sezione Botanica Sistematica, Via G. La Pira 4, I-50121 Firenze, Italy 4 Author for correspondence ( [email protected] ) Communicating Editor: Lena Struwe Abstract— Boraginaceae tribe Trigonotideae comprises a heterogenous assemblage of taxa, many of which have been shown to belong to widely divergent lineages in Boraginaceae in the recent past, with some taxa now assigned to three of the four currently recognized tribes of the Boraginaceae s. s., namely the Cynoglosseae, Echiochileae, and Lithospermeae. The systematics of Moritzia and Thaumatocaryon , the only endemic South American genera of Boraginaceae, have been controversially discussed in the past, and their most recent placement was in Trigonotideae. The present study investigates the phylogenetic relationships of “Trigonotideae” based on micromorphology and molecular data (ITS including 5.8S rRNA, and the trnL-trnF spacer). Molecular data show that “Trigonotideae” are polyphyletic, and none of its mem- bers is at all closely related to Trigonotis itself. Moritzia and Thaumatocaryon are closely allied to each other and are the sister group of the Old World Boragineae. Flowers, pollen, and fruit morphology strongly support this systematic placement. -
Galanthus Woronowii Losinsk., Amaryllidaceae
Modern Phytomorphology 6: 59–66, 2014 SOME MORPHOLOGICAL AND ANATOMICAL DESCRIPTIONS OF SEED IN GALANTHUS WORONOWII LOSINSK. FROM WESTERN GEORGIA Nona Chkhaidze 1*, Nana Goginashvili 1**, Meri Zurabishvili 1***, Zurab Manvelidze 2 Abstract. Morphology and anatomy of seeds of Galanthus woronowii Losinsk. from Ajara and Guria (Western Georgia) regions were studied in laboratory conditions. It was found out that shape of fruits changed from round (big fruits) to longish (small fruits). Weight of mature seed was 0,0075 g. By the end of June elaiosome disappears and green hollow develops on its place. Gas bubbles were emitted from green tissues; emission was intensive in August, when embryo was already well developed. Greenness was localized mainly on cell walls. It is permissible that on cells walls located aerobic oxygenic phototrophic bacteria. In early August an embryo in seeds was well developed, reserve fat transformed to starch around of embryo. Germination of seeds began by the end September very slowly. Results of the work will be important for ex situ conservation of G. woronowii, also for expedient to plant industrial plantations. Key words: Galanthus woronowii, seed, morphology, anatomy, development 1 Agricultural University of Georgia, University Campus of Digomi, David Aghmashenebeli Alley 140, 0159 Tbilisi, Georgia; * [email protected], ** [email protected], *** [email protected] 2 Batumi Botanical Garden, Mtsvane kontskhi, 6010 Batumi, Georgia Introduction on the base of recommendations of CITES Secretariat and Georgian Scientific Authority The bulbous ephemerid Woronow’s(CITES 2008). In spite of the fact that natural snowdrop (Galanthus woronowii Losinsk., stock of the plant in Western Georgia is about Amaryllidaceae) is widely spread in Colchic 300 million bulbs (CITES 2008) and the forests of Western Georgia. -
“Redirecting” the Study of Mutualistic Benefits to Plants in Myrmecochory
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Faculty Publications and Other Works -- Ecology and Evolutionary Biology Ecology and Evolutionary Biology Fall 2014 “Redirecting” the Study of Mutualistic Benefits oT Plants In Myrmecochory Mariah Taylor Patton [email protected] Follow this and additional works at: https://trace.tennessee.edu/utk_ecolpubs Recommended Citation Patton, Mariah T. "“Redirecting” the study of mutualistic benefits ot plants in myrmecochory" (2014). University of Tennessee Honors Thesis Projects. This Article is brought to you for free and open access by the Ecology and Evolutionary Biology at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Faculty Publications and Other Works -- Ecology and Evolutionary Biology by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. “Redirecting” the study of mutualistic benefits to plants in myrmecochory By Mariah Patton Mentor: Dr. Charles Kwit 1 Abstract Myrmecochory is typically cast as a mutualistic relationship in which seed dispersal of plants with elaiosome-bearing seeds is performed by ants. Benefits of this mutualism may seem simple at first: ants gain a nutritive reward via elaiosomes, while plant propagules gain protection and a more suitable microsite for establishment and growth. However, there is growing literature suggesting that ants may not consistently receive benefits from elaiosome-based diets, and studies depicting plant benefits are constrained by the “ideal” model framework, by temporal limitations, and by limitations of sources of mortality that have typically been investigated. Furthermore, from the plant perspective, many key parts as well as inconsistencies within this more complex process have not been well explored.