Gooseberry Globemallow (Sphaeralcea Grossulariifolia)
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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. -
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. -
Germination and Seedling Establishment of Spiny Hopsage (Grayia Spinosa [Hook.] Moq.)
AN ABSTRACT OF THE THESIS OF Nancy L. Shaw for the degree of Doctor of Philosophy in Crop and Soil Sciences presented on March 19, 1992 Title: Germination and Seedling Establishment of Spiny Hopsage (Grayia Spinosa [Hook.] Moq.) Abstract approved:_Redactedfor Privacy von r. ULdUe Reestablishment of spiny hopsage(Grayia spinosa [Hook.] Moq.) where depleted or lost on shrub steppe sites can improve forage, plant cover, and soil stabilization. The objectives of this study were to: 1) determine direct-seeding requirements; 2) develop optimum germination pretreatments; and 3) examine dormancy mechanisms in spiny hopsage fruits and seeds. The effects of seed source, planting date,and site preparation method onseed germination and seedling establishment (SE) were examined at Birds of Prey and Reynolds Creek in southwestern Idaho. Three seed sources were planted on rough or compact seedbeds on 4 dates in 1986-87 and 3 dates in 1987-88. Exposure to cool-moist environments improved spring SE from early fall (EF) and late fall (LF) plantings. Few seedlings emerged from early (ESp) or late spring (LSp) plantings. SE was low at: 1 site in 1986-87 and atboth sites in 1987-88, probably due to lack of precipitation. For the successful 1986-87 planting, seedling density was greater on rough compared to compact seedbeds in April andMay, possiblydue to improved microclimate conditions. Growth rate varied among seed sources, but seedlings developed a deep taproot (mean length 266 mm) with few lateral roots the first season. Seeds were planted on 3 dates in 1986-87 and 1987-88, andnylon bags containing seeds were planted on 4 dates each year to study microenvironment effects on germination (G), germination rate (GR), and SE. -
Heterodichogamy.Pdf
Research Update TRENDS in Ecology & Evolution Vol.16 No.11 November 2001 595 How common is heterodichogamy? Susanne S. Renner The sexual systems of plants usually Heterodichogamy differs from normal (Zingiberales). These figures probably depend on the exact spatial distribution of dichogamy, the temporal separation of underestimate the frequency of the gamete-producing structures. Less well male and female function in flowers, in heterodichogamy. First, the phenomenon known is how the exact timing of male and that it involves two genetic morphs that is discovered only if flower behavior is female function might influence plant occur at a 1:1 ratio. The phenomenon was studied in several individuals and in mating. New papers by Li et al. on a group discovered in walnuts and hazelnuts5,6 natural populations. Differential of tropical gingers describe differential (the latter ending a series of Letters to movements and maturation of petals, maturing of male and female structures, the Editor about hazel flowering that styles, stigmas and stamens become such that half the individuals of a began in Nature in 1870), but has gone invisible in dried herbarium material, population are in the female stage when almost unnoticed7. Indeed, its recent and planted populations deriving from the other half is in the male stage. This discovery in Alpinia was greeted as a vegetatively propagated material no new case of heterodichogamy is unique new mechanism, differing ‘from other longer reflect natural morph ratios. The in involving reciprocal movement of the passive outbreeding devices, such as discovery of heterodichogamy thus styles in the two temporal morphs. dichogamy…and heterostyly in that it depends on field observations. -
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. -
Inflorescence Dimorphism, Heterodichogamy and Thrips
Annals of Botany 113: 467–476, 2014 doi:10.1093/aob/mct278, available online at www.aob.oxfordjournals.org Inflorescence dimorphism, heterodichogamy and thrips pollination in Platycarya strobilacea (Juglandaceae) Tatsundo Fukuhara* and Shin-ichiro Tokumaru Faculty of Education, Fukuoka University of Education, 1-1 Akama-Bunkyo-machi, Munakata, Fukuoka, Japan * For correspondence. E-mail [email protected] Received: 22 July 2013 Returned for revision: 11 September 2013 Accepted: 14 October 2013 Published electronically: 3 December 2013 † Background and Aims Unlike other taxa in Juglandaceae or in closely related families, which are anemophilous, Platycarya strobilacea has been suggested to be entomophilous. In Juglandaceae, Juglans and Carya show hetero- dichogamy, a reproductive strategy in which two morphs coexist in a population and undergo synchronous reciprocal sex changes. However, there has been no study focusing on heterodichogamy in the other six or seven genera, includ- ing Platycarya. † Methods Inflorescence architecture, sexual expression and pollination biology were examined in a P. strobilacea population in Japan. Flowering phenology was monitored daily for 24 trees in 2008 and 27 in 2009. Flower visitors and inhabitants were recorded or collected from different sexes and stages. † Key results The population of P. strobilacea showed heterodichogamous phenology with protogynous and duodi- chogamous–protandrous morphs. This dimorphism in dichogamy was associated with distinct inflorescence morph- ologies.Thrips pollination was suggested bythe frequent presence of thrips withattached pollen grains,the scarcityof other insect visitors, the synchronicity of thrips number in male spikes with the maturation of female flowers, and morphological characters shared with previously reported thrips-pollinated plants. Male spikes went through two consecutive stages: bright yellow and strong-scented M1 stage, and brownish and little-scented M2 stage. -
Gardening for Native Bees in Utah and Beyond James H
Published by Utah State University Extension and Utah Plant Pest Diagnostic Laboratory ENT-133-09 January 2013 Gardening for Native Bees in Utah and Beyond James H. Cane Linda Kervin Research Entomologist, USDA ARS Logan, UT Pollinating Insect-Biology, Management, Systematics Research Do You Know? • 900 species of native bees reside in Utah. • Some wild bees are superb pollinators of Utah’s tree fruits, raspberries, squashes, melons and cucumbers. • Few of our native bees have much venom or any inclination to sting. • Our native bees use hundreds of varieties of garden flowers, many of them water-wise. • A garden plant need not be native to attract and feed native bees. tah is home to more than 20 percent Uof the 4,000+ named species of wild Fig. 1. Carder bee (Anthidium) foraging at lavender (Lavendula: Lamiaceae).1 bees that are native to North America. Except for bumblebees and some sweat bees, our native bees are solitary, not so- cial, many with just one annual generation that coincides with bloom by their favorite floral hosts. In contrast, the familiar honey- bee is highly social, has perennial colonies, and was brought to North America by settlers from Europe. Regardless of these differences, however, all of our bees need pollen and nectar from flowers. The sugars in sweet nectar power their flight; mother bees also imbibe some nectar to mix with pollen that they gather. Pollen is fortified with proteins, oils and minerals that are es- sential for the diets of their grub-like larvae back at the nest. Our flower gardens can become valuable cafeterias for local populations of diverse native bees. -
A New Large-Flowered Species of Andeimalva (Malvaceae, Malvoideae) from Peru
A peer-reviewed open-access journal PhytoKeys 110: 91–99 (2018) A new large-flowered species of Andeimalva... 91 doi: 10.3897/phytokeys.110.29376 RESEARCH ARTICLE http://phytokeys.pensoft.net Launched to accelerate biodiversity research A new large-flowered species of Andeimalva (Malvaceae, Malvoideae) from Peru Laurence J. Dorr1, Carolina Romero-Hernández2, Kenneth J. Wurdack1 1 Department of Botany, MRC-166, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington, D.C. 20013-7012, USA 2 Missouri Botanical Garden Herbarium, William L. Brown Center, P.O. Box 299, Saint Louis, MO 63166-0299, USA Corresponding author: Laurence J. Dorr ([email protected]) Academic editor: Clifford Morden | Received 28 August 2018 | Accepted 11 October 2018 | Published 5 November 2018 Citation: Dorr LJ, Romero-Hernández C, Wurdack KJ (2018) A new large-flowered species ofAndeimalva (Malvaceae: Malvoideae) from Peru. PhytoKeys 110: 91–99. https://doi.org/10.3897/phytokeys.110.29376 Abstract Andeimalva peruviana Dorr & C.Romero, sp. nov., the third Peruvian endemic in a small genus of five species, is described and illustrated from a single collection made at high elevation on the eastern slopes of the Andes. Molecular phylogenetic analyses of nuclear ribosomal ITS sequence data resolve a group of northern species of Andeimalva found in Bolivia and Peru from the morphologically very different south- ern A. chilensis. The new species bears the largest flowers of anyAndeimalva and is compared with Bolivian A. mandonii. A revised key to the genus is presented. Keywords Andeimalva, Andes, Malvaceae, Malvoideae, Peru, phylogeny Introduction The genus Andeimalva J.A. Tate (Malvaceae, Malvoideae) was created to accommo- date four species found in the Andes of South America from northern Peru to central Chile and includes three species previously placed in Tarasa Phil. -
Caryophyllales: a Key Group for Understanding Wood
Botanical Journal of the Linnean Society, 2010, 164, 342–393. With 21 figures Caryophyllales: a key group for understanding wood anatomy character states and their evolutionboj_1095 342..393 SHERWIN CARLQUIST FLS* Santa Barbara Botanic Garden, 1212 Mission Canyon Road, Santa Barbara, CA 93110, USA Received 13 May 2010; accepted for publication 28 September 2010 Definitions of character states in woods are softer than generally assumed, and more complex for workers to interpret. Only by a constant effort to transcend the limitations of glossaries can a more than partial understanding of wood anatomy and its evolution be achieved. The need for such an effort is most evident in a major group with sufficient wood diversity to demonstrate numerous problems in wood anatomical features. Caryophyllales s.l., with approximately 12 000 species, are such a group. Paradoxically, Caryophyllales offer many more interpretive problems than other ‘typically woody’ eudicot clades of comparable size: a wider range of wood structural patterns is represented in the order. An account of character expression diversity is presented for major wood characters of Caryophyllales. These characters include successive cambia (more extensively represented in Caryophyllales than elsewhere in angiosperms); vessel element perforation plates (non-bordered and bordered, with and without constrictions); lateral wall pitting of vessels (notably pseudoscalariform patterns); vesturing and sculpturing on vessel walls; grouping of vessels; nature of tracheids and fibre-tracheids, storying in libriform fibres, types of axial parenchyma, ray anatomy and shifts in ray ontogeny; juvenilism in rays; raylessness; occurrence of idioblasts; occurrence of a new cell type (ancistrocladan cells); correlations of raylessness with scattered bundle occurrence and other anatomical discoveries newly described and/or understood through the use of scanning electron microscopy and light microscopy. -
Review and Advances in Style Curvature for the Malvaceae Cheng-Jiang Ruan*
® International Journal of Plant Developmental Biology ©2010 Global Science Books Review and Advances in Style Curvature for the Malvaceae Cheng-Jiang Ruan* Key Laboratory of Biotechnology & Bio-Resources Utilization, Dalian Nationalities University, Dalian City, Liaoning 116600, China Correspondence : * [email protected] ABSTRACT The flowers of the Malvaceae with varying levels of herkogamy via style curvature have long intrigued evolutionary botanists. This review covers the flower opening process, approach herkogamy, style curvature and character evolution based on molecular phylogenetic trees, adaptive significances of style curvature and the mating system in some portions of the genera in this family. Hermaphroditic flowers of some species have showy petals and pollen and nectar rewards to pollinators. Approach herkogamy, in which stigmas are located on the top of a monadelphous stamen, has evolved as a mechanism to reduce the frequency of intra-floral self-pollination or the interference between male-female organs. Protandrous or monochogamous flowers in the fields open at about 5-7 days and 1-2 days respectively, and pollination is conducted by insects and birds. Interestingly, un-pollinated styles in some species curve when pollination fails. According to our observations and published or internet data, this curvature occurs in 23 species distributed in eight genera of four tribes (Malvavisceae, Ureneae, Hibisceae, Malveae) and appears to have evolved at least eight times. A shift to use style curvature is associated with a shift to annual or perennial herbs, and an unpredictable pollinator environment is likely an important trigger for this evolution. The adaptive significances of style curvature in the Malvaceae include delayed selfing, promotion of outcrossing or reduction in intrafloral male-female interference, sometimes two or three of which simultaneously occur in style curvature of one species (e.g., Kosteletzkya virginica). -
Chenopodioideae, Chenopodiaceae/ Amaranthaceae): Implications for Evolution and Taxonomy
Fruit and Seed Anatomy of Chenopodium and Related Genera (Chenopodioideae, Chenopodiaceae/ Amaranthaceae): Implications for Evolution and Taxonomy Alexander P. Sukhorukov1,2*, Mingli Zhang1,3 1 Key Laboratory of Biogeography and Bioresource in Arid Land, Xinjiang Institute of Ecology and Geography, Chinese Academy of Sciences, Urumqi, Xinjiang, China, 2 Department of Higher Plants, Biological Faculty, Moscow Lomonosov State University, Moscow, Russia, 3 Institute of Botany, Chinese Academy of Sciences, Beijing, China Abstract A comparative carpological study of 96 species of all clades formerly considered as the tribe Chenopodieae has been conducted for the first time. The results show important differences in the anatomical structure of the pericarp and seed coat between representatives of terminal clades including Chenopodium s.str.+Chenopodiastrum and the recently recognized genera Blitum, Oxybasis and Dysphania. Within Chenopodium the most significant changes in fruit and seed structure are found in members of C. sect. Skottsbergia. The genera Rhagodia and Einadia differ insignificantly from Chenopodium. The evolution of heterospermy in Chenopodium is discussed. Almost all representatives of the tribe Dysphanieae are clearly separated from other Chenopodioideae on the basis of a diverse set of characteristics, including the small dimensions of the fruits (especially in Australian taxa), their subglobose shape (excl. Teloxys and Suckleya), and peculiarities of the pericarp indumentum. The set of fruit and seed characters evolved within the subfamily Chenopodioideae is described. A recent phylogenetic hypothesis is employed to examine the evolution of three (out of a total of 21) characters, namely seed color, testa-cell protoplast characteristics and embryo orientation. Citation: Sukhorukov AP, Zhang M (2013) Fruit and Seed Anatomy of Chenopodium and Related Genera (Chenopodioideae, Chenopodiaceae/Amaranthaceae): Implications for Evolution and Taxonomy. -
WOOD ANATOMY of CHENOPODIACEAE (AMARANTHACEAE S
IAWA Journal, Vol. 33 (2), 2012: 205–232 WOOD ANATOMY OF CHENOPODIACEAE (AMARANTHACEAE s. l.) Heike Heklau1, Peter Gasson2, Fritz Schweingruber3 and Pieter Baas4 SUMMARY The wood anatomy of the Chenopodiaceae is distinctive and fairly uni- form. The secondary xylem is characterised by relatively narrow vessels (<100 µm) with mostly minute pits (<4 µm), and extremely narrow ves- sels (<10 µm intergrading with vascular tracheids in addition to “normal” vessels), short vessel elements (<270 µm), successive cambia, included phloem, thick-walled or very thick-walled fibres, which are short (<470 µm), and abundant calcium oxalate crystals. Rays are mainly observed in the tribes Atripliceae, Beteae, Camphorosmeae, Chenopodieae, Hab- litzieae and Salsoleae, while many Chenopodiaceae are rayless. The Chenopodiaceae differ from the more tropical and subtropical Amaran- thaceae s.str. especially in their shorter libriform fibres and narrower vessels. Contrary to the accepted view that the subfamily Polycnemoideae lacks anomalous thickening, we found irregular successive cambia and included phloem. They are limited to long-lived roots and stem borne roots of perennials (Nitrophila mohavensis) and to a hemicryptophyte (Polycnemum fontanesii). The Chenopodiaceae often grow in extreme habitats, and this is reflected by their wood anatomy. Among the annual species, halophytes have narrower vessels than xeric species of steppes and prairies, and than species of nitrophile ruderal sites. Key words: Chenopodiaceae, Amaranthaceae s.l., included phloem, suc- cessive cambia, anomalous secondary thickening, vessel diameter, vessel element length, ecological adaptations, xerophytes, halophytes. INTRODUCTION The Chenopodiaceae in the order Caryophyllales include annual or perennial herbs, sub- shrubs, shrubs, small trees (Haloxylon ammodendron, Suaeda monoica) and climbers (Hablitzia, Holmbergia).