Munro's Globemallow Plant Guide
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Southwestern Rare and Endangered Plants
Preliminary Report on the Reproductive Biology of the Threatened Chisos Mountain Hedgehog Cactus BONNIE B. AMOS and CHRISTOS VASSILIOU Angelo State University, Texas Abstract: The Chisos Mountain hedgehog cactus (Echinocereus chisoensis, Cactaceae) is a narrow endemic restricted to an approximately 100 square mile area in Big Bend National Park, Texas. It was listed as threatened in 1987 as Echinocereus chisoensis var. chisoensis. An investigation of the reproductive biology and pollination ecology conducted in 1999 and 2000 revealed the taxon to be homogamous, self-incompatible, xenogamous, and heavily dependent upon the cactus oligolectic bee, Diadasia rinconis (Anthophoridae) for pollination. Despite infrequent bee visitation, fruit set from open pollination is high and fruits produce large numbers of seeds. Predation in 2002, probably from rodents as a result of severe drought conditions, was severe on plants, flower buds, and fruits. The Chisos Mountain hedgehog cactus, or Chisos jillo (Opuntia leptocaulis DC.), ocotillo (Fouquieria pitaya (Echinocereus chisoensis W. Marshall), is 1 of splendens K. Kunth), leatherstem (Jatropha dioica V. 20 threatened or endangered cacti listed by the de Cervantes), lechuguilla (Agave lechuguilla J. U.S. Fish and Wildlife Service for Region 2 (http: Torrey), and ceniza (Leucophyl1umf)zltescens (J. Ber- // ecos. fws.gov/ webpage/ webpage-lead.htrnl? landier) I. M. Johnston). An earlier study (Hender- lead_region=2&type=L&listings=l).In 1987 it was shott et al. 1992) did not show specific E. chisoen- added to the federal lists (53 FR 38453) of en- sis-nurse plant associations, but rather showed dangered and threatened wildlife and plants as associations as a consequence of soil conditions threatened because of its restricted distribution, that provide a hospitablL environment for a diver- low numbers, loss of viability in existing popula- sity of species or the exploitation by E. -
Sphaeralcea Coccinea Scarlet Globemallow
Sphaeralcea coccinea Scarlet Globemallow by Kathy Lloyd Montana Native Plant Society Photo: Drake Barton Sphaeralcea coccinea (Scarlet Globemallow) is not an authentic Lewis and Clark collection. They believe the scarlet globemallow plants on that sheet carlet globemallow, a member of the mallow were grown from seed collected by Thomas Nuttall family (Malvaceae) was collected by in 1811. The other specimen sheet contains plants SMeriwether Lewis on July 20, 1806 along the Marias collected by Meriwether Lewis in Montana. The River in present-day Toole County. On the same label on the specimen, applied by the botanist day he also collected Gardner’s saltbush (Atriplex Frederick Pursh, says, “A malvaceous Small plant gardneri) and greasewood (Sarcobatus probably a Species of Malope. Plains of Missouri. vermiculatus). Lewis and his small band of men Jul. 20th 1806.” Lewis, always the eager naturalist, were attempting to follow the Marias River drainage took time to write in his journal that day, “the wild north to determine where the river began. They liquorice and sunflower are very abundant in the were hoping to claim land for the United States to plains and river bottoms, the latter is now in full the most northern parallel of the Missouri River blume; the silkgrass and sand rush are also system. Although Lewis did not succeed in staking common.” a claim for more land, he did make significant Scarlet globemallow occurs in dry grassland discoveries that advanced the knowledge of the prairies and plains from Alberta, Saskatchewan, and flora, fauna, ecology, and soils in the area west of Manitoba in Canada, south and eastward to Arizona, the Mississippi River. -
Classification of the Apidae (Hymenoptera)
Utah State University DigitalCommons@USU Mi Bee Lab 9-21-1990 Classification of the Apidae (Hymenoptera) Charles D. Michener University of Kansas Follow this and additional works at: https://digitalcommons.usu.edu/bee_lab_mi Part of the Entomology Commons Recommended Citation Michener, Charles D., "Classification of the Apidae (Hymenoptera)" (1990). Mi. Paper 153. https://digitalcommons.usu.edu/bee_lab_mi/153 This Article is brought to you for free and open access by the Bee Lab at DigitalCommons@USU. It has been accepted for inclusion in Mi by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. 4 WWvyvlrWryrXvW-WvWrW^^ I • • •_ ••^«_«).•>.• •.*.« THE UNIVERSITY OF KANSAS SCIENC5;^ULLETIN LIBRARY Vol. 54, No. 4, pp. 75-164 Sept. 21,1990 OCT 23 1990 HARVARD Classification of the Apidae^ (Hymenoptera) BY Charles D. Michener'^ Appendix: Trigona genalis Friese, a Hitherto Unplaced New Guinea Species BY Charles D. Michener and Shoichi F. Sakagami'^ CONTENTS Abstract 76 Introduction 76 Terminology and Materials 77 Analysis of Relationships among Apid Subfamilies 79 Key to the Subfamilies of Apidae 84 Subfamily Meliponinae 84 Description, 84; Larva, 85; Nest, 85; Social Behavior, 85; Distribution, 85 Relationships among Meliponine Genera 85 History, 85; Analysis, 86; Biogeography, 96; Behavior, 97; Labial palpi, 99; Wing venation, 99; Male genitalia, 102; Poison glands, 103; Chromosome numbers, 103; Convergence, 104; Classificatory questions, 104 Fossil Meliponinae 105 Meliponorytes, -
GOOSEBERRYLEAF GLOBEMALLOW Sphaeralcea Grossulariifolia (Hook
GOOSEBERRYLEAF GLOBEMALLOW Sphaeralcea grossulariifolia (Hook. & Arn.) Rydb. Malvaceae – Mallow family Corey L. Gucker & Nancy L. Shaw | 2018 ORGANIZATION NOMENCLATURE Sphaeralcea grossulariifolia (Hook. & Arn.) Names, subtaxa, chromosome number(s), hybridization. Rydb., hereafter referred to as gooseberryleaf globemallow, belongs to the Malveae tribe of the Malvaceae or mallow family (Kearney 1935; La Duke 2016). Range, habitat, plant associations, elevation, soils. NRCS Plant Code. SPGR2 (USDA NRCS 2017). Subtaxa. The Flora of North America (La Duke 2016) does not recognize any varieties or Life form, morphology, distinguishing characteristics, reproduction. subspecies. Synonyms. Malvastrum coccineum (Nuttall) A. Gray var. grossulariifolium (Hooker & Arnott) Growth rate, successional status, disturbance ecology, importance to animals/people. Torrey, M. grossulariifolium (Hooker & Arnott) A. Gray, Sida grossulariifolia Hooker & Arnott, Sphaeralcea grossulariifolia subsp. pedata Current or potential uses in restoration. (Torrey ex A. Gray) Kearney, S. grossulariifolia var. pedata (Torrey ex A. Gray) Kearney, S. pedata Torrey ex A. Gray (La Duke 2016). Seed sourcing, wildland seed collection, seed cleaning, storage, Common Names. Gooseberryleaf globemallow, testing and marketing standards. current-leaf globemallow (La Duke 2016). Chromosome Number. Chromosome number is stable, 2n = 20, and plants are diploid (La Duke Recommendations/guidelines for producing seed. 2016). Hybridization. Hybridization occurs within the Sphaeralcea genus. -
Globemallows
RANGELANDS15(3), June 1993 127 Globemallows Bruce M. Pendery and Melvin D. Rumbaugh We initiated research on the ecological and forage ona, New Mexico, and Texas have the most species. characteristicsof globemallows(Sphaeralcea) in 1986 Sphaeralcea coccinea is the most widely distributed during a search for beneficialforbs that are well adapted species. to cold desertand steppe rangelands receivingless than Generally, globemallowspecies in the U.S. are peren- 12 inches of precipitation annually. Globemallows are nial, cool-season forbs or half-shrubs (Shaw andMonsen well adapted to such stressful environments. They also 1983, Pendery and Rumbaugh 1986). Most have showy are native species, which may be desired or required in orangeflowers borneon multiple stems that arise from a some situations. basalcrown. However, S. coccinea is moreprostrate and spreadsby rhizomes. In the western U.S. globemallows Characteristics and Ecology grow best in open or disturbed sites (especially road- Globemallows (see cover photos)are in the family Mal- sides) on sandy- to clay-loamsoils, or on gravelly foot- vaceae,which includes species such as cotton, okra, and hills receivingabout 8 to 12 inches of precipitationannu- hollyhock. Sphaeralcea occurs primarily in North and ally (Wasser 1982). Sphaeralcea grossulariifoliais found South America (Kearney 1935). There are 25 globemal- on alkaline soils and tolerates moderate salinity, but it low species on western U.S. rangelands (Table 1). Ariz- does not tolerate sodic soils. Recentwork hasshed lighton globemallowlife-history This article is a cooperativeinvestigation of the USDA-ARS and the Utah Agricultural ExperimentStation, Logan,Utah. Journal PaperNo. 4384. strategies,which may improveour management abilities. Authors are range scientist and retired Research Geneticist, respectively, Under natural conditions establish USDA,Agricultural Research Service, Logan.Utah 84322-6300. -
Components of Nest Provisioning Behavior in Solitary Bees (Hymenoptera: Apoidea)*
Apidologie 39 (2008) 30–45 Available online at: c INRA/DIB-AGIB/ EDP Sciences, 2008 www.apidologie.org DOI: 10.1051/apido:2007055 Review article Components of nest provisioning behavior in solitary bees (Hymenoptera: Apoidea)* John L. Neff Central Texas Melittological Institute, 7307 Running Rope, Austin, Texas 78731, USA Received 13 June 2007 – Revised 28 September 2007 – Accepted 1 October 2007 Abstract – The components of nest provisioning behavior (resources per cell, transport capacity, trip dura- tion, trips per cell) are examined for a data set derived from the literature and various unpublished studies. While there is a trade-off between transport capacity and trips required per cell, the highest provisioning rates are achieved by bees carrying very large pollen loads at intermediate trip durations. Most solitary bees appear to be either egg or resource limited, so sustained provisioning rates over one cell per day are unusual. Provisioning rate / body size / transport capacity / solitary bees / trip duration 1. INTRODUCTION tradeoffs between provisioning one large cell or two small cells direct, indirect, or nonex- There is a vast literature on the foraging tac- istent? Are provisioning rates related to body tics of bees: what kinds of flowers to visit, how size? long to spend on a flower, how many flowers Provisioning rate is a general term and can in an inflorescence to visit, when to turn, and simply refer to the rate (mass per unit time) so forth. Much of this work is done within a at which foragers bring various food items framework of whether a forager should max- (pollen, nectar, oils, carrion, or whatever) to imize harvesting rate or foraging efficiency their nests. -
Novitates PUBLISHED by the AMERICAN MUSEUM of NATURAL HISTORY CENTRAL PARK WEST at 79TH STREET, NEW YORK, N.Y
AMERICAN MUSEUM Novitates PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK, N.Y. 10024 Number 2640, pp. 1-24, figs. 1-36, tables 1-3 January 3, 1978 The Bionomics and Immature Stages of the Cleptoparasitic Bee Genus Protepeolus (Anthophoridae, Nomadinae) JEROME G. ROZEN, JR.,' KATHLEEN R. EICKWORT,2 AND GEORGE C. EICKWORT3 ABSTRACT Protepeolus singularis was found attacking cells numerous biological dissimilarities. The first in- in nests of Diadasia olivacea in southeastern Ari- star Protepeolus attacks and kills the pharate last zona. The following biological information is pre- larval instar of the host before consuming the sented: behavior of adult females while searching provisions, a unique feature for nomadine bees. for host nests; intraspecific interactions of fe- First and last larval instars and the pupa are males at the host nesting site; interactions with described taxonomically and illustrated. Brief host adults; oviposition; and such larval activities comparative descriptions of the other larval in- as crawling, killing the host, feeding, defecation, stars are also given. Larval features attest to the and cocoon spinning. In general, adult female be- common origin of Protepeolus and the other havior corresponds to that of other Nomadinae. Nomadinae. Cladistic analysis using 27 characters Females perch for extended periods near nest of mature larvae of the Nomadinae demonstrates entrances and avoid host females, which attack that Isepeolus is a sister group to all the other parasites when encountered. Females apparently Nomadinae known from larvae, including Pro- learn the locations of host nests and return to tepeolus, and that Protepeolus is a sister group to them frequently. -
The Impact of Molecular Data on Our Understanding of Bee Phylogeny and Evolution
EN58CH04-Danforth ARI 5 December 2012 7:55 The Impact of Molecular Data on Our Understanding of Bee Phylogeny and Evolution Bryan N. Danforth,1∗ Sophie Cardinal,2 Christophe Praz,3 Eduardo A.B. Almeida,4 and Denis Michez5 1Department of Entomology, Cornell University, Ithaca, New York 14853; email: [email protected] 2Canadian National Collection of Insects, Agriculture Canada, Ottawa, Ontario K1A 0C6, Canada; email: [email protected] 3Institute of Biology, University of Neuchatel, Emile-Argand 11, 2009 Neuchatel, Switzerland; email: [email protected] 4Departamento de Biologia, FFCLRP-Universidade de Sao˜ Paulo, 14040-901 Ribeirao˜ Preto, Sao˜ Paulo, Brazil; email: [email protected] 5University of Mons, Laboratory of Zoology, 7000 Mons, Belgium; email: [email protected] Annu. Rev. Entomol. 2013. 58:57–78 Keywords First published online as a Review in Advance on Hymenoptera, Apoidea, bees, molecular systematics, sociality, parasitism, August 28, 2012 plant-insect interactions The Annual Review of Entomology is online at ento.annualreviews.org Abstract by 77.56.160.109 on 01/14/13. For personal use only. This article’s doi: Our understanding of bee phylogeny has improved over the past fifteen years 10.1146/annurev-ento-120811-153633 as a result of new data, primarily nucleotide sequence data, and new methods, Copyright c 2013 by Annual Reviews. primarily model-based methods of phylogeny reconstruction. Phylogenetic All rights reserved Annu. Rev. Entomol. 2013.58:57-78. Downloaded from www.annualreviews.org studies based on single or, more commonly, multilocus data sets have helped ∗ Corresponding author resolve the placement of bees within the superfamily Apoidea; the relation- ships among the seven families of bees; and the relationships among bee subfamilies, tribes, genera, and species. -
Effects of Invasive Plant Species on Native Bee Communities in the Southern Great Plains
EFFECTS OF INVASIVE PLANT SPECIES ON NATIVE BEE COMMUNITIES IN THE SOUTHERN GREAT PLAINS By KAITLIN M. O’BRIEN Bachelor of Science in Rangeland Ecology & Management Texas A&M University College Station, Texas 2015 Submitted to the Faculty of the Graduate College of the Oklahoma State University in partial fulfillment of the requirements for the Degree of MASTER OF SCIENCE May, 2017 EFFECTS OF INVASIVE PLANT SPECIES ON NATIVE BEE COMMUNITIES IN THE SOUTHERN GREAT PLAINS Thesis Approved: Dr. Kristen A. Baum Thesis Adviser Dr. Karen R. Hickman Dr. Dwayne Elmore ii ACKNOWLEDGEMENTS I would like to begin by thanking my advisor, Dr. Kristen Baum, for all of her guidance and expertise throughout this research project. She is an exemplary person to work with, and I am so grateful to have shared my graduate school experience with her. I would also like to recognize my committee members, Dr. Karen Hickman and Dr. Dwayne Elmore, both of whom provided valuable insight to this project. A huge thank you goes out to the Southern Plains Network of the National Park Service, specifically Robert Bennetts and Tomye Folts-Zettner. Without them, this project would not exist, and I am forever grateful to have been involved with their network and parks, both as a research student and summer crew member. A special thank you for Jonathin Horsely, who helped with plot selection, summer sampling, and getting my gear around. I would also like to thank the Baum Lab members, always offering their support and guidance as we navigated through graduate school. And lastly, I would like to thank my family, especially my fiancé Garrett, for believing in me and supporting me as I pursued my goals. -
Bee-Friendly Native Plants
BEE-FRIENDLY NATIVE PLANTS Theodore Payne Foundation for Wild Flowers and Native Plants 10459 Tuxford Street, Sun Valley, CA 91352 | (818) 768-1802 | theodorepayne.org California is home to 1,600 native bee species! Native bees are important and effective pollinators and essential to a healthy ecosystem. The best way to support these and other beneficial insects in your garden is to provide them with native plants. ANNUALS (best sown from seed in fall) Clarkia unguiculata (elegant clarkia) Showy white, pink or magenta flowers on tall upright stems. Foliage is used by sphinx moth caterpillars (also called hummingbird moths!). Eschscholzia californica (California poppy) Favored by small sweat bees and our smallest bees, Perdita spp. Gilia capitata (globe gilia) Late-spring bloomer loved by long-horned bees. Layia platyglossa (tidy tips) Cheerful yellow and white daisy-like flowers. Lupinus succulentus (arroyo lupine) and other species Blue-purple flowers attract bumblebees. Mentzelia lindleyi Golden yellow flowers attract digger bees Nemophila menziesii (baby blue eyes) Charming little plant with blue flowers. Grows well in part sun to shade. Phacelia tanacetifolia (tansy-leaved phacelia) A must-have for any bee garden. PERENNIALS Calystegia macrostegia (morning glory) Climbing vine attracts the specialist digger bee, Diadasia bituberculata, which forages only on this flower. Helianthus annuus (common sunflower), Baileya multiradiata (desert marigold) and other Aster family species Attract many pollinators, including sweat bees, mason bees and bumble bees. Monardella spp. (coyote mint) Fragrant foliage and showy, nectar-rich flowers attract bees, flower flies and butterflies. Penstemon spectabilis (showy penstemon) Large tubular flowers are foraged by bees and pollen wasps. -
Insect Pollination of Prickly-Pears (Opuntia: Cactaceae) Author(S): Bruce D
Southwestern Association of Naturalists Insect Pollination of Prickly-Pears (Opuntia: Cactaceae) Author(s): Bruce D. Parfitt and Charles H. Pickett Source: The Southwestern Naturalist, Vol. 25, No. 1 (Jan. 30, 1980), pp. 104-107 Published by: Southwestern Association of Naturalists Stable URL: http://www.jstor.org/stable/3671218 Accessed: 13-11-2015 20:21 UTC Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at http://www.jstor.org/page/ info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Southwestern Association of Naturalists is collaborating with JSTOR to digitize, preserve and extend access to The Southwestern Naturalist. http://www.jstor.org This content downloaded from 156.40.216.1 on Fri, 13 Nov 2015 20:21:54 UTC All use subject to JSTOR Terms and Conditions I t:Y ~oIL I tsF `.'4 ...,'',' "-,,,'., ',", Fig. 1. Nests of Osprey (upper) and Great Blue Heron in cardon cactus, Tiburon Island, Sonora, May 1978. almost immediately. The heron returned within a few minutes and attempted to alight on its nest. It made three attemptsby approaching from above and passing over or alongside the Osprey nest. In each case it was driven off by the Osprey. On its fourthattempt it approached the nest fromthe frontand below, apparently not disturbingthe Osprey, and was permittedto settle on its nest. -
Differences in Arthropods Found in Flowers Versus Trapped in Plant
Arthropod-Plant Interactions (2014) 8:411–419 DOI 10.1007/s11829-014-9328-x ORIGINAL PAPER Differences in arthropods found in flowers versus trapped in plant resins on Haplopappus platylepis Phil. (Asteraceae): Can the plant discriminate between pollinators and herbivores? Cristian A. Villagra • Alvaro Astudillo Meza • Alejandro Urzu´a Received: 30 September 2013 / Accepted: 25 August 2014 / Published online: 26 September 2014 Ó Springer Science+Business Media Dordrecht 2014 Abstract Plants produce secondary metabolites related to insects we observed foraging on disk florets; Arthrobracus ecologically relevant processes. These compounds include (Coleoptera: Melyridae) and Linepithema (Hymenoptera: surface secretions such as latex, mucilage and resins that Formicidae) were the predominant insects ‘‘trapped in help plants face abiotic and biotic environmental threats resin’’, while Diadasia (Hymenoptera: Apidae) was the such as drought, nutrient deficiency, extreme temperatures most frequent ‘‘floral visitor’’. We propose that bracteal and UV radiation, as well as herbivory, pathogenic resin of H. platylepis may function as a selective trap for microorganisms and other natural enemies. We studied the non-mutualistic insects reaching reproductive structures of resinous coating found on involucral bracts of Haplopap- this plant and discuss other multiple possible roles for this pus platylepis Phil. (Asteraceae). This plant belongs to a secretion, including protocarnivory. speciose genus widely distributed in South America (Lane and Hartman in Am J Bot 83:356, 1996). H. platylepis is Keywords Constitutive resistance Á Terpenoids Á characterized by resinous fragrant leaves. In this species, Larcenist Á Diadasia chilensis Á Lioptilodes friasi resins cover the involucral bracts as well as young leaves and are also secreted on reproductive stalks in smaller amounts.