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Caterpillars Moths Butterflies Woodies
NATIVE Caterpillars Moths and utter flies Band host NATIVE Hackberry Emperor oodies PHOTO : Megan McCarty W Double-toothed Prominent Honey locust Moth caterpillar Hackberry Emperor larva PHOTO : Douglas Tallamy Big Poplar Sphinx Number of species of Caterpillars n a study published in 2009, Dr. Oaks (Quercus) 557 Beeches (Fagus) 127 Honey-locusts (Gleditsia) 46 Magnolias (Magnolia) 21 Double-toothed Prominent ( Nerice IDouglas W. Tallamy, Ph.D, chair of the Cherries (Prunus) 456 Serviceberry (Amelanchier) 124 New Jersey Tea (Ceanothus) 45 Buttonbush (Cephalanthus) 19 bidentata ) larvae feed exclusively on elms Department of Entomology and Wildlife Willows (Salix) 455 Larches or Tamaracks (Larix) 121 Sycamores (Platanus) 45 Redbuds (Cercis) 19 (Ulmus), and can be found June through Ecology at the University of Delaware Birches (Betula) 411 Dogwoods (Cornus) 118 Huckleberry (Gaylussacia) 44 Green-briar (Smilax) 19 October. Their body shape mimics the specifically addressed the usefulness of Poplars (Populus) 367 Firs (Abies) 117 Hackberry (Celtis) 43 Wisterias (Wisteria) 19 toothed shape of American elm, making native woodies as host plants for our Crabapples (Malus) 308 Bayberries (Myrica) 108 Junipers (Juniperus) 42 Redbay (native) (Persea) 18 them hard to spot. The adult moth is native caterpillars (and obviously Maples (Acer) 297 Viburnums (Viburnum) 104 Elders (Sambucus) 42 Bearberry (Arctostaphylos) 17 small with a wingspan of 3-4 cm. therefore moths and butterflies). Blueberries (Vaccinium) 294 Currants (Ribes) 99 Ninebark (Physocarpus) 41 Bald cypresses (Taxodium) 16 We present here a partial list, and the Alders (Alnus) 255 Hop Hornbeam (Ostrya) 94 Lilacs (Syringa) 40 Leatherleaf (Chamaedaphne) 15 Honey locust caterpillar feeds on honey number of Lepidopteran species that rely Hickories (Carya) 235 Hemlocks (Tsuga) 92 Hollies (Ilex) 39 Poison Ivy (Toxicodendron) 15 locust, and Kentucky coffee trees. -
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
Bulletin of Natural History ®
FLORI'IDA MUSEUM BULLETIN OF NATURAL HISTORY ® A MIDDLE EOCENE FOSSIL PLANT ASSEMBLAGE (POWERS CLAY PIT) FROM WESTERN TENNESSEE DavidL. Dilcher and Terry A. Lott Vol. 45, No. 1, pp. 1-43 2005 UNIVERSITY OF FLORIDA GAINESVILLE - The FLORIDA MUSEUM OF NATURAL HiSTORY is Florida«'s state museum of natural history, dedicated to understanding, preser¥ingrand interpreting].biologica[1 diversity and culturafheritage. The BULLETIN OF THE FLORIDA- MUSEUM OF NATURAL HISTORY is a peer-reviewed publication thatpziblishes.the result5 of origifial reseafchin zodlogy, botany, paleontology, and archaeology. Address all inquiries t6 the Managing Editor ofthe Bulletin. Numbers,ofthe Bulletin,afe,published,at itregular intervals. Specific volumes are not'necessarily completed in anyone year. The end of a volume willl·be noted at the foot of the first page ofthe last issue in that volume. Richard Franz, Managing Editor Erika H. Simons, Production BulletinCommittee Richard Franz,,Chairperson Ann Cordell Sarah Fazenbaker Richard Hulbert WilliamMarquardt Susan Milbrath Irvy R. Quitmyer - Scott Robinson, Ex 01#cio Afember ISSN: 0071-6154 Publication Date: October 31,2005 Send communications concerning purchase or exchange of the publication and manustfipt queries to: Managing Editor of the BULLETIN Florida MuseumofNatural-History University offlorida PO Box 117800 Gainesville, FL 32611 -7800 U.S.A. Phone: 352-392-1721 Fax: 352-846-0287 e-mail: [email protected] A MIDDLE EOCENE FOSSIL PLANT ASSEMBLAGE (POWERS CLAY PIT) FROM WESTERN TENNESSEE David L. Dilcher and Terry A. Lottl ABSTRACT Plant megafossils are described, illustrated and discussed from Powers Clay Pit, occurring in the middle Eocene, Claiborne Group of the Mississippi Embayment in western Tennessee. -
Trillium, As an Indicator of Deer Density Hanover Biodiversity Committee October, 2017
[DRAFT v. 10] Trillium, as an indicator of deer density Hanover Biodiversity Committee October, 2017 Rationale for this Report Members of the lily family, such as Trillium and Clintonia, are among the favored foods of deer; 30 species of Trillium are found East of the Mississippi. The decline of these plants is mentioned in multiple publications1 as one key indicator of deer over-abundance. Red Trillium (Trillium erectum), also called ‘wake Robin’, found in the north-east and is (or was) fairly common in many Hanover forested neighborhoods. We suggest that monitoring this plant where it is (or once was) common demonstrates that deer density remains unsustainably high and future monitoring of the plant can help determine both the neighborhood density of deer and also serve as an indicator of change in deer density. Monitoring for this plant is easy, with just a small bit of training about the process. This report suggests a serious decline in biodiversity in Hanover over the past 15 years, as indicated by impact on red Trillium at three sites. We believe that with a focused increase in hunting pressure, this and other declining native plants might recover. Red Trillium is a frequent member of typical ‘rich mesic forests2’ plant communities found in Hanover; other plants often found nearby are Virginia waterleaf, blood root, wild ginger, foam flower, blue cohosh, and certain other members of the lily family. Besides aggressive deer browse, these communities are also threatened in varying degrees by invasive plants: garlic mustard, Dame’s rocket, wild parsnip, wild chervil and forget-me-not as well as the usual woody invaders. -
The Evolution of a Sex Chromosome in Asparagus by Alex E. Harkess (Under the Direction of James H. Leebens-Mack) Abstract the Ov
The Evolution of a Sex Chromosome in Asparagus by Alex E. Harkess (Under the Direction of James H. Leebens-Mack) Abstract The overwhelming majority of flowering plants reproduce through the production of hermaphroditic flowers. A small percentage of angiosperm species instead are dioecious, producing either male or female flowers on individual plants. Dioecy can be mediated at the molecular level by a sex chromosome that genetically differentiates males and females. Sex chromosomes evolve from autosomes, and this conversion is hypothesized to involve muta- tions in one or more linked genes that determine sex. Given the complexities of anther and ovule development, the full suite of sex determination genes has not been described for any dioecious plant. Here we explore the conversion from autosome to an XY sex chromosome using garden asparagus (Asparagus officinalis), an ideal model system for studying the ear- liest events in sex chromosome evolution given that it recently evolved a sex chromosome pair. Focusing first on broad trends, genomic characterization of several hermaphroditic and dioecious species across the Asparagus genus revealed an increase in retrotransposon con- tent coincident with the evolution of dioecy. To identify putative sex determination genes on this Y chromosome, we then explore the timing of male and female sterility events in garden asparagus, hypothesizing that anther sterility in females likely occurs before pollen microsporogenesis. Finally, we assemble and annotate a high quality reference genome for garden asparagus, and perform a suite of mutant analyses to identify two genes in a non- recombining region of the Y that are ultimately responsible for sex determination. -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
Late Pliocene Smilax (Smilacaceae) Leaves from Southwest China: Phytogeo- Graphical and Paleoecological Implications
ÔØ ÅÒÙ×Ö ÔØ Late Pliocene Smilax (Smilacaceae) leaves from Southwest China: Phytogeo- graphical and paleoecological implications Jing-Yu Wu, Yu-Sheng (Christopher) Liu, Su-Ting Ding, Jun Li, Peng- Cheng An PII: S0034-6667(16)30158-0 DOI: doi:10.1016/j.revpalbo.2017.02.006 Reference: PALBO 3841 To appear in: Review of Palaeobotany and Palynology Received date: 26 August 2016 Revised date: 19 February 2017 Accepted date: 20 February 2017 Please cite this article as: Wu, Jing-Yu, Liu, Yu-Sheng (Christopher), Ding, Su-Ting, Li, Jun, An, Peng-Cheng, Late Pliocene Smilax (Smilacaceae) leaves from Southwest China: Phytogeographical and paleoecological implications, Review of Palaeobotany and Palynology (2017), doi:10.1016/j.revpalbo.2017.02.006 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. ACCEPTED MANUSCRIPT Late Pliocene Smilax (Smilacaceae) leaves from Southwest China: phytogeographical and paleoecological implications Jing-Yu Wua,b*, Yu-Sheng (Christopher) Liuc, Su-Ting Dinga,b, Jun Lia, Peng-Cheng Ana a Key Laboratory of Mineral Resources in Western China (Gansu Province), School of Earth Sciences, and College of Earth and Environmental Sciences, Lanzhou University, Lanzhou 730000, China b State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, China cOffice of Research and Graduate Studies, Prairie View A & M University, Prairie View, TX 77446, USA *Correspondence (Email: [email protected]). -
Greenbrier (Catbrier) Family
SMILACACEAE – GREENBRIER (CATBRIER) FAMILY Plant: mostly woody vines, some herbs and shrubs Stem: often with tendrils, spines common in some Root: often with tubers Leaves: evergreen, mostly simple, alternate (sometimes opposite) and entire; one veined or mostly 3-7 curved, parallel main veins with net veins between; tendrils often present, stipules present or not Flowers: mostly dioecious, some perfect; flower parts (tepals) in 3’s in 2 cycles of 6; stamens vary but often 6; ovary superior Fruit: berry, 1-6 but often 3 seeds Other: Carrion Flower is the only non-woody greenbrier in the area; Monocotyledons Group Genera: 3-12 (uncertain); locally Smilax (greenbrier or catbrier) WARNING – family descriptions are only a layman’s guide and should not be used as definitive SMILACACEAE – GREENBRIER (CATBRIER) FAMILY Saw [Fringed] Greenbrier; Smilax bona-nox L. Upright Carrion-Flower; Smilax ecirrhata (Engelm. Ex Kunth) S. Watson Cat Greenbrier [Sawbrier]; Smilax glauca Walter Smooth Carrion-Flower; Smilax herbacea L. Illinois Greenbrier; Smilax illinoensis Mangaly Round Leaved [Common] Greenbrier; Smilax rotundifolia L. Bristly Greenbrier [Catbrier]; Smilax tamnoides L. Saw [Fringed] Greenbrier USDA Smilax bona-nox L. Smilacaceae (Greenbrier Family) Tybee Island, Georgia Notes: flower with 6 tepals, greenish; leaves alternate, simple, often hastate (arrowhead shaped) or at least with a deltoid base, leaf margins thickened and spinose, tip sharp-pointed; stem green, at least 1+ angled and spinose; fruits dark blue to black; late spring to summer -
Liliaceae Lily Family
Liliaceae lily family While there is much compelling evidence available to divide this polyphyletic family into as many as 25 families, the older classification sensu Cronquist is retained here. Page | 1222 Many are familiar as garden ornamentals and food plants such as onion, garlic, tulip and lily. The flowers are showy and mostly regular, three-merous and with a superior ovary. Key to genera A. Leaves mostly basal. B B. Flowers orange; 8–11cm long. Hemerocallis bb. Flowers not orange, much smaller. C C. Flowers solitary. Erythronium cc. Flowers several to many. D D. Leaves linear, or, absent at flowering time. E E. Flowers in an umbel, terminal, numerous; leaves Allium absent. ee. Flowers in an open cluster, or dense raceme. F F. Leaves with white stripe on midrib; flowers Ornithogalum white, 2–8 on long peduncles. ff. Leaves green; flowers greenish, in dense Triantha racemes on very short peduncles. dd. Leaves oval to elliptic, present at flowering. G G. Flowers in an umbel, 3–6, yellow. Clintonia gg. Flowers in a one-sided raceme, white. Convallaria aa. Leaves mostly cauline. H H. Leaves in one or more whorls. I I. Leaves in numerous whorls; flowers >4cm in diameter. Lilium ii. Leaves in 1–2 whorls; flowers much smaller. J J. Leaves 3 in a single whorl; flowers white or purple. Trillium jj. Leaves in 2 whorls, or 5–9 leaves; flowers yellow, small. Medeola hh. Leaves alternate. K K. Flowers numerous in a terminal inflorescence. L L. Plants delicate, glabrous; leaves 1–2 petiolate. Maianthemum ll. Plant coarse, robust; stems pubescent; leaves many, clasping Veratrum stem. -
Plant and Wildlife List, Geology Summary, Resources
ROCK CREEK PARK PLANT & WILDLIFE LIST PEIRCE MILL AREA Smithsonian Associates Nature/History Hike & Virtual Presentation with Melanie Choukas-Bradley, Author of A Year in Rock Creek Park, City of Trees, Finding Solace at Theodore Roosevelt Island & forest bathing books July 2021 Woody Plants (*Non-Natives) Trees unless identified as Shrub or Vine Acer negundo Box-Elder or Ash-Leaved Maple Acer platanoides Norway Maple* Acer rubrum Red Maple Acer saccharum Sugar Maple Acer saccharinum Silver Maple Ailanthus altissima Ailanthus or Tree of Heaven* Albizia julibrissin Mimosa or Silk-Tree* Amelanchier Shadbush or Serviceberry Asimina triloba Pawpaw Betula nigra River Birch Carpinus caroliniana American Hornbeam, Ironwood or Musclewood Carya cordiformis Bitternut Hickory Carya glabra Pignut Hickory Carya illinoinensis Pecan (planted) Carya ovata Shagbark Hickory (planted) Carya laciniosa Shellbark Hickory (planted) Carya tomentosa Mockernut Hickory (C. alba) Catalpa speciosa Northern Catalpa (native to the midwest; naturalized) Cercis canadensis Redbud Cornus florida Flowering Dogwood Diospyros virginiana Persimmon Euonymus alatus Winged Euonymus or Burning Bush* (shrub) Euonymus americanus Strawberry Bush (shrub) Fagus grandifolia American Beech Fraxinus americana White Ash Fraxinus pennsylvanica Green Ash Hamamelis virginiana Witch-Hazel (shrub or small tree with yellow late- autumn flowers) Hydrangea arborescens Hydrangea, Wild (shrub) Ilex opaca American Holly Juglans nigra Black Walnut Juniperus virginiana Eastern Red-Cedar, Virginia Juniper 2 | P a g e Kalmia latifolia Mountain Laurel (evergreen shrub) Lindera benzoin Spicebush (shrub) Liquidambar styraciflua Sweetgum (planted near Peirce Mill & Milkhouse Ford) Liriodendron tulipifera Tulip-Tree (Tulip Poplar) Lonicera maackii Maack’s Honeysuckle* (shrub) Magnolia grandiflora Southern Magnolia (planted) Magnolia macrophylla Bigleaf Magnolia (naturalized from the south) Magnolia tripetala Umbrella Magnolia Malus spp. -
What Is a Similax Vine? Q: in the Last Year, Smilax, Cat Briar, Or
What is a Similax vine? Q: In the last year, smilax, cat briar, or blaspheme vine has become a real problem in my shrubs. Cutting the vines is only a very short relief, and the darn things seem immune to RoundUp. I want to kill them down to the bottom of the tuber. Suggestions? Photo courtesy Hans Hillewaert Smilax can be ornamental, but the thornier vines are more often just a nuisance. A: Smilax is a vine exquisitely adapted to the South and our Southern gardening habits. If we could only find a way to make use of it ... There are many species of smilax, and I can’t help but point out that some varieties of smilax, particularly the nearly thornless Jackson vine, are not only quite ornamental, but also quite delicious (the young stems are exceptional, like a nutty asparagus). The small trailing smilax of longleaf woodlands (Smilax pumila) is one of the most graceful and ornamental groundcovers for Southern yards. And coral greenbrier (Smilax walteri) produces some of the most beautiful fruits of any Southern vine. Yes, honest to goodness, I treasure some of my smilax. But there’s no denying: The thornier smilax vines, the ones with the more- or-less heart-shaped leaves, can be a nuisance. Once those leathery leaves harden off in spring, they won’t absorb common foliar herbicides such as RoundUp. And while the very young and soft leaves are susceptible to herbicide in March and early April, it can be hard to get them to absorb enough herbicide to carry it into the thick, underground root system. -
SPRING WILDFLOWERS of OHIO Field Guide DIVISION of WILDLIFE 2 INTRODUCTION This Booklet Is Produced by the ODNR Division of Wildlife As a Free Publication
SPRING WILDFLOWERS OF OHIO field guide DIVISION OF WILDLIFE 2 INTRODUCTION This booklet is produced by the ODNR Division of Wildlife as a free publication. This booklet is not for resale. Any By Jim McCormac unauthorized reproduction is prohibited. All images within this booklet are copyrighted by the Division of Wild- life and it’s contributing artists and photographers. For additional information, please call 1-800-WILDLIFE. The Ohio Department of Natural Resources (ODNR) has a long history of promoting wildflower conservation and appreciation. ODNR’s landholdings include 21 state forests, 136 state nature preserves, 74 state parks, and 117 wildlife HOW TO USE THIS GUIDE areas. Collectively, these sites total nearly 600,000 acres Bloom Calendar Scientific Name (Scientific Name Pronunciation) Scientific Name and harbor some of the richest wildflower communities in MID MAR - MID APR Definition BLOOM: FEB MAR APR MAY JUN Ohio. In August of 1990, ODNR Division of Natural Areas and Sanguinaria canadensis (San-gwin-ar-ee-ah • can-ah-den-sis) Sanguinaria = blood, or bleeding • canadensis = of Canada Preserves (DNAP), published a wonderful publication entitled Common Name Bloodroot Ohio Wildflowers, with the tagline “Let Them Live in Your Eye Family Name POPPY FAMILY (Papaveraceae). 2 native Ohio species. DESCRIPTION: .CTIGUJQY[ƃQYGTYKVJPWOGTQWUYJKVGRGVCNU Not Die in Your Hand.” This booklet was authored by the GRJGOGTCNRGVCNUQHVGPHCNNKPIYKVJKPCFC[5KPINGNGCHGPYTCRU UVGOCVƃQYGTKPIVKOGGXGPVWCNN[GZRCPFUKPVQCNCTIGTQWPFGFNGCH YKVJNQDGFOCTIKPUCPFFGGRDCUCNUKPWU