Nomenclatural Notes About the Names in Amaranthaceae Published by Roberto De Visiani
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Plant Guide for Fourwing Saltbush (Atriplex Canescens)
Plant Guide saline-sodic soils (Ogle and St. John, 2008). It has FOURWING SALTBUSH excellent drought tolerance and has been planted in highway medians and on road shoulders, slopes, and other Atriplex canescens (Pursh) Nutt. disturbed areas near roadways. Because it is a good Plant Symbol = ATCA2 wildlife browse species, caution is recommended in using fourwing saltbush in plantings along roadways. Its Contributed by: USDA NRCS Idaho Plant Materials extensive root system provides excellent erosion control. Program Reclamation: fourwing saltbush is used extensively for reclamation of disturbed sites (mine lands, drill pads, exploration holes, etc,). It provides excellent species diversity for mine land reclamation projects. Status Please consult the PLANTS Web site and your State Department of Natural Resources for this plant’s current status (e.g., threatened or endangered species, state noxious status, and wetland indicator values). Description Fourwing saltbush is a polymorphic species varying from deciduous to evergreen, depending on climate. Its much- branched stems are stout with whitish bark. Mature plants range from 0.3 to 2.4 m (1 to 8 ft) in height, depending on ecotype and the soil and climate. Its leaves are simple, alternate, entire, linear-spatulate to narrowly oblong, Fourwing saltbush. Photo by Steven Perkins @ USDA-NRCS canescent (covered with fine whitish hairs) and ½ to 2 PLANTS Database inches long. Its root system is branched and commonly very deep reaching depths of up to 6 m (20 ft) when soil Alternate Names depth allows (Kearney et al., 1960). Common Alternate Names: Fourwing saltbush is mostly dioecious, with male and Chamise, chamize, chamiso, white greasewood, saltsage, female flowers on separate plants (Welsh et al., 2003); fourwing shadscale, bushy atriplex however, some monoecious plants may be found within a population. -
The Vascular Plants of Massachusetts
The Vascular Plants of Massachusetts: The Vascular Plants of Massachusetts: A County Checklist • First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Somers Bruce Sorrie and Paul Connolly, Bryan Cullina, Melissa Dow Revision • First A County Checklist Plants of Massachusetts: Vascular The A County Checklist First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Massachusetts Natural Heritage & Endangered Species Program Massachusetts Division of Fisheries and Wildlife Natural Heritage & Endangered Species Program The Natural Heritage & Endangered Species Program (NHESP), part of the Massachusetts Division of Fisheries and Wildlife, is one of the programs forming the Natural Heritage network. NHESP is responsible for the conservation and protection of hundreds of species that are not hunted, fished, trapped, or commercially harvested in the state. The Program's highest priority is protecting the 176 species of vertebrate and invertebrate animals and 259 species of native plants that are officially listed as Endangered, Threatened or of Special Concern in Massachusetts. Endangered species conservation in Massachusetts depends on you! A major source of funding for the protection of rare and endangered species comes from voluntary donations on state income tax forms. Contributions go to the Natural Heritage & Endangered Species Fund, which provides a portion of the operating budget for the Natural Heritage & Endangered Species Program. NHESP protects rare species through biological inventory, -
Underutilization Versus Nutritional-Nutraceutical Potential of the Amaranthus Food Plant: a Mini-Review
applied sciences Review Underutilization Versus Nutritional-Nutraceutical Potential of the Amaranthus Food Plant: A Mini-Review Olusanya N. Ruth 1,*, Kolanisi Unathi 1,2, Ngobese Nomali 3 and Mayashree Chinsamy 4 1 Disipline of Food Security, School of Agricultural, Earth and Environmental Science University of KwaZulu-Natal, Scottsville, Pietermaritzburg 3209, South Africa; [email protected] 2 Department of Consumer Science, University of Zululand, 24 Main Road, KwaDlangezwa, Uthungulu 3886, South Africa 3 Department of Botany and Plant Biotectechnology, University of Johannesburg, Auckland Park, Johannesburg 2092, South Africa; [email protected] 4 DST-NRF-Center, Indiginous Knowledge System, University of KwaZulu-Natal, Westville 3629, South Africa; [email protected] * Correspondence: [email protected] Abstract: Amaranthus is a C4 plant tolerant to drought, and plant diseases and a suitable option for climate change. This plant could form part of every region’s cultural heritage and can be transferred to the next generation. Moreover, Amaranthus is a multipurpose plant that has been identified as a traditional edible vegetable endowed with nutritional value, besides its fodder, medicinal, nutraceutical, industrial, and ornamental potentials. In recent decade Amaranthus has received increased research interest. Despite its endowment, there is a dearth of awareness of its numerous potential benefits hence, it is being underutilized. Suitable cultivation systems, innovative Citation: Ruth, O.N.; Unathi, K.; processing, and value-adding techniques to promote its utilization are scarce. However, a food-based Nomali, N.; Chinsamy, M. approach has been suggested as a sustainable measure that tackles food-related problem, especially Underutilization Versus in harsh weather. Thus, in this review, a literature search for updated progress and potential Nutritional-Nutraceutical Potential of uses of Amaranthus from online databases of peer-reviewed articles and books was conducted. -
Chisel-Toothed Kangaroo Rat (Dipodomys Microps Alfredi)
Version 2020-04-20 [A race of the] Chisel-toothed Kangaroo Rat (Dipodomys microps alfredi) Species Status Statement. Distribution This subspecies is endemic to Utah and occurs only on Gunnison Island in the Great Salt Lake. Durrant (1952, p. 274) considered this kangaroo rat to be the most distinctive of the mammal subspecies that are endemic to islands in the Great Salt Lake—so distinctive that he even considered the possibility that it may deserve full species status. Table 1. Utah counties currently occupied by this species. [a Race of the] Chisel-toothed Kangaroo Rat - alfredi BOX ELDER Abundance and Trends Oliver (field notes, 15 July 2014 and 22 October 2014) captured numerous individuals on the north and south sides of Gunnison Island. However, its population trends are unknown. Statement of Habitat Needs and Threats to the Species. Habitat Needs The chisel-toothed kangaroo rat (Dipodomys microps, full species) is a dietary and a habitat specialist, and typically lives in association with either saltbush (Atriplex sp.) or blackbrush (Coleogyne sp.). However in some places it is found in association with greasewood (Sarcobatus sp.), sagebrush (Artemisia sp.), and a few other desert shrubs. Native perennial grasses are thought to be well-tolerated by the species, but introduced annual grasses are considered to impact it negatively (see review of ecology in Hayssen 1991). Threats to the Species The State of Utah owns Gunnison Island, and the Utah Division of Wildlife Resources administers it as a bird nesting colony. Therefore many potential anthropogenic threats are already prevented. The principal threat to the existence of Dipodomys microps alfredi is the dewatering of the Great Salt Lake. -
(Amaranthaceae) in Italy. V. Atriplex Tornabenei
Phytotaxa 145 (1): 54–60 (2013) ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2013 Magnolia Press ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.145.1.6 Studies on the genus Atriplex (Amaranthaceae) in Italy. V. Atriplex tornabenei DUILIO IAMONICO1 1 Laboratory of Phytogeography and Applied Geobotany, Department PDTA, Section Environment and Landscape, University of Rome Sapienza, 00196 Roma, Italy. Email: [email protected] Abstract The typification of the name Atriplex tornabenei (a nomen novum pro A. arenaria) is discussed. An illustration by Cupani is designated as the lectotype, while a specimen from FI is designated as the epitype. Chorological and morphological notes in comparison with the related species A. rosea and A. tatarica are also provided. A nomenclatural change (Atriplex tornabenei subsp. pedunculata stat. nov.) is proposed. Key words: Atriplex tornabenei var. pedunculata, epitype, infraspecific variability, lectotype, Mediterranean, nomenclatural change, nomen novum Introduction Atriplex Linnaeus (1753: 1054) is a genus of about 260 species distributed in arid and semiarid regions of Eurasia, America and Australia (Sukhorukov & Danin 2009). Several names (at species, subspecies, variety and form ranks) were described related to the high phenotipic variability of this critical genus (Al-Turki et al. 2000). As conseguence, misapplication of names and nomenclatural disorders exist and need clarification. In this paper, the identity of the A. tornabenei Tineo ex Gussone (1843: 589) is discussed as part of the treatment of the genus Atriplex for the new edition of the Italian Flora (editor, Prof. S. Pignatti) and within the initiative “Italian Loci Classici Census” (Domina et al. -
Origin and Age of Australian Chenopodiaceae
ARTICLE IN PRESS Organisms, Diversity & Evolution 5 (2005) 59–80 www.elsevier.de/ode Origin and age of Australian Chenopodiaceae Gudrun Kadereita,Ã, DietrichGotzek b, Surrey Jacobsc, Helmut Freitagd aInstitut fu¨r Spezielle Botanik und Botanischer Garten, Johannes Gutenberg-Universita¨t Mainz, D-55099 Mainz, Germany bDepartment of Genetics, University of Georgia, Athens, GA 30602, USA cRoyal Botanic Gardens, Sydney, Australia dArbeitsgruppe Systematik und Morphologie der Pflanzen, Universita¨t Kassel, D-34109 Kassel, Germany Received 20 May 2004; accepted 31 July 2004 Abstract We studied the age, origins, and possible routes of colonization of the Australian Chenopodiaceae. Using a previously published rbcL phylogeny of the Amaranthaceae–Chenopodiaceae alliance (Kadereit et al. 2003) and new ITS phylogenies of the Camphorosmeae and Salicornieae, we conclude that Australia has been reached in at least nine independent colonization events: four in the Chenopodioideae, two in the Salicornieae, and one each in the Camphorosmeae, Suaedeae, and Salsoleae. Where feasible, we used molecular clock estimates to date the ages of the respective lineages. The two oldest lineages both belong to the Chenopodioideae (Scleroblitum and Chenopodium sect. Orthosporum/Dysphania) and date to 42.2–26.0 and 16.1–9.9 Mya, respectively. Most lineages (Australian Camphorosmeae, the Halosarcia lineage in the Salicornieae, Sarcocornia, Chenopodium subg. Chenopodium/Rhagodia, and Atriplex) arrived in Australia during the late Miocene to Pliocene when aridification and increasing salinity changed the landscape of many parts of the continent. The Australian Camphorosmeae and Salicornieae diversified rapidly after their arrival. The molecular-clock results clearly reject the hypothesis of an autochthonous stock of Chenopodiaceae dating back to Gondwanan times. -
Understanding the Weedy Chenopodium Complex in the North Central States
UNDERSTANDING THE WEEDY CHENOPODIUM COMPLEX IN THE NORTH CENTRAL STATES BY SUKHVINDER SINGH DISSERTATION Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Crop Sciences in the Graduate College of the University of Illinois at Urbana-Champaign, 2010 Urbana, Illinois Doctoral Committee: Professor Patrick J. Tranel, Chair Associate Professor Aaron G. Hager Associate Professor Geoffrey A. Levin Assistant Professor Matthew E. Hudson ABSTRACT The genus Chenopodium consists of several important weed species, including Chenopodium album, C. berlandieri, C. strictum, and C. ficifolium. All of these species share similar vegetative morphology and high phenotypic plasticity, which makes it difficult to correctly identify these species. All of these weedy Chenopodium species have developed resistance to one or more classes of herbicides. An experiment was conducted to determine if there is variability in response of Chenopodium species present in the North Central states to glyphosate. Our results indicate variable responses within and among the Chenopodium species. Species such as C. berlandieri and C. ficifolium had higher levels of tolerance to glyphosate than did various accessions of C. album. In another experiment, 33 populations of Chenopodium sampled across six North Central states were screened with glyphosate. The results showed variable responses to glyphosate within and among the Chenopodium populations. In general, the Chenopodium populations from Iowa were more tolerant, but some biotypes from North Dakota, Indiana and Kansas also had significantly high tolerance to glyphosate. Given there are species other than C. album that have high tolerance to glyphosate, and there are Chenopodium populations across the North Central states that showed tolerance to glyphosate, one intriguing question was to whether the Chenopodium populations were either biotypes of C. -
Amaranthaceae Amaranth Family
Amaranthaceae Amaranth Family Mostly ruderal annuals, there are 900 species in 65 genera. A single genus reaches Nova Scotia. Their flowers are inconspicuous, green and apetalous, subtended by papery bracts. Flowers are unisexual Page | 108 although the plants are monoecious. The terminal inflorescence is brushlike or axillary. A single lens- shaped achene is produced. Some are flowering ornamentals, such as Celosia and Love-lies-bleeding (Amaranthus caudatus) and others are used for grain. Amaranthus L. Three of 50 species have been introduced into Nova Scotia. Key to species A. A. Plants slender, branching diffusely; flowers in small axillary clusters; Amaranthus albus seeds small, <0.8mm wide. aa. Plants robust, erect; flowers in large terminal inflorescences; seeds >1mm B wide. B. Leaves green beneath; sepals pointed. A. hybridus bb. Leaves whitish beneath; sepals truncate. A. retroflexus Amaranthus albus L. Tumbleweed; amarante blanche An erect herb, its stems are freely branching. Leaves are elliptic or oblanceolate, borne on petioles. Flowers are arranged in dense axillary clusters. July to October, on disturbed soils. Uncommon and appearing as a garden weed or about railways. Collected from Truro, Wentworth, Windsor and Kentville. Ranges from western Canada to Mexico. Introduced throughout most of the continent. 3-2 Amaranthaceae Amaranthus hybridus L. Green Amaranth; amarante verte Tall and robust, its stem reaches to 2m in height, often branching freely. Stems are scaly or lightly pubescent Page | 109 especially in the inflorescence. Flowers are reddish, not showy. Leaves are elliptic and petiolate. August to October. A weed of disturbed soils and cultivated fields. It is limited to a few well-established populations: Morristown and other communities in Kings Co. -
Beta Vulgaris (Common Beet) Class:Magnoliopsida Order
Beta vulgaris (Common Beet) Class:Magnoliopsida Order: Caryophyllales Family: Amaranthaceae Genus: Beta Species: Beta vulgaris Beet seeds Common Varieties: Bull’s Blood, Golden, Chioggia, Detroit Dark Red How to Save Seed Beets are a biennial crop, meaning they require two years to complete their full growing cycle. However, most growers never see this second stage of life because beets are harvested for food during the first year. The second year heralds seed production. To save the seeds from beta vulgaris, the beets themselves must be overwintered. This process, unique to perennial and biennial crops, requires that the taproot of the beta vulgaris (the edible part of the beet) be stored in a protected place during the winter months. A Seed Saving Guide asserts that the optimal temperature range for winter storage is between 35-38F at 90-95% humidity. The roots may be stored in sawdust or wood shavings to minimize rot. This allows the plant to enter a period of dormancy—during this time, the plant’s energy will be diverted to the next year’s seed production. In Spring, plant the overwintered beets outside in a well-watered trench. Because beets are wind-pollinated, they should be planted in a block formation rather than a straight row to ensure proper pollination. The Seed Saver’s Exchange Seed Saving Guide specifies that the isolation distance (the distance between different varieties of beets) must be over 800 feet. Adhering to this distance is critical—without it, there is potential for varieties to cross-pollinate, meaning the genetic integrity of the beet variety will be compromised. -
Table 4: Pollen-Types in Amaranthaceae by Mittre (1963). Amaranthus-Type
Table 4: Pollen-types in Amaranthaceae by Mittre (1963). Amaranthus-type Amaranthus- type sensu stricto Cyathula-type Celosia-type Pollen Faintly to moderately granulate Prominently granulate Baculariate morphological characters: Sexine pattern Total number of 5 2 2 genera studied Genera Amaranthus spinosus L., Cyathula prostrate (L.) Blume, Celosia argentea L., C. cristata L., A. viridis L., A. tricolor L., C. capitata Moq., Allmania albida (Willd.) R.Br. ex Hook.f., A. hybridus L., Deeringia celosioides R.Br. A. nodiflora (L.) R.Br. ex Wight. A. polygamous L., A. tenuifolius Willd., A. spinosus L., Achyranthes aspera L., A. bidentata Blume, Aerva lanata (L.) Juss., A. sanguinolenta (L.) Blume, A. tomentosa Forssk., A. javanica (Burm.f.) Juss. ex Schult., A. monsoniae (L. f.) Mart., Digera arvensis Forssk., Pupalia lappacea (L.) Juss., P. atropurpurea (Lam.) Moq. 22 Table 4: Continued. Gomphrena-type Gomphrena-type sensu stricto Alternanthera-type Not included in any group Pollen reticulate several meshes, without reticulate with few meshes, without reticulate with several meshes and spinulate morphological spinules spinules characters: Sexine pattern Total number of 1 1 1 genera studied Genera Gomphrena globosa L., Alternanthera sessilis (L.) R.Br. ex DC., Psilotrichum ferrugineum (Roxb.) Moq. G. celosioides Mart. A. repens J.F.Gmel. 2 3 Table 5: Pollen-types in Centrospermae by Nowicke (1975). Type I Type II Type III Pollen morphological 3- Colpate Pantoporate Pantocolpate characters: apertures Family studied Aizoaceae, Cactaceae, Caryophyllaceae, Amaranthaceae, Cactaceae, Basellaceae, Cactaceae, Molluginaceae, Nyctaginaceae, Caryophyllaceae, Chenopodiaceae, Molluginaceae, Nyctaginaceae, Phytolaccaceae, Portulacaceae Dysphaniaceae, Nyctaginaceae, Phytolaccaceae, Portulacaceae Phytolaccaceae, Portulacaceae Genera studied in 11 Amaranthaceae Species studied in Amaranthus spinosus L., Amaranthaceae Aerva leucura Moq., Allmania nodiflora (L.) R.Br. -
Literaturverzeichnis
Literaturverzeichnis Abaimov, A.P., 2010: Geographical Distribution and Ackerly, D.D., 2009: Evolution, origin and age of Genetics of Siberian Larch Species. In Osawa, A., line ages in the Californian and Mediterranean flo- Zyryanova, O.A., Matsuura, Y., Kajimoto, T. & ras. Journal of Biogeography 36, 1221–1233. Wein, R.W. (eds.), Permafrost Ecosystems. Sibe- Acocks, J.P.H., 1988: Veld Types of South Africa. 3rd rian Larch Forests. Ecological Studies 209, 41–58. Edition. Botanical Research Institute, Pretoria, Abbadie, L., Gignoux, J., Le Roux, X. & Lepage, M. 146 pp. (eds.), 2006: Lamto. Structure, Functioning, and Adam, P., 1990: Saltmarsh Ecology. Cambridge Uni- Dynamics of a Savanna Ecosystem. Ecological Stu- versity Press. Cambridge, 461 pp. dies 179, 415 pp. Adam, P., 1994: Australian Rainforests. Oxford Bio- Abbott, R.J. & Brochmann, C., 2003: History and geography Series No. 6 (Oxford University Press), evolution of the arctic flora: in the footsteps of Eric 308 pp. Hultén. Molecular Ecology 12, 299–313. Adam, P., 1994: Saltmarsh and mangrove. In Groves, Abbott, R.J. & Comes, H.P., 2004: Evolution in the R.H. (ed.), Australian Vegetation. 2nd Edition. Arctic: a phylogeographic analysis of the circu- Cambridge University Press, Melbourne, pp. marctic plant Saxifraga oppositifolia (Purple Saxi- 395–435. frage). New Phytologist 161, 211–224. Adame, M.F., Neil, D., Wright, S.F. & Lovelock, C.E., Abbott, R.J., Chapman, H.M., Crawford, R.M.M. & 2010: Sedimentation within and among mangrove Forbes, D.G., 1995: Molecular diversity and deri- forests along a gradient of geomorphological set- vations of populations of Silene acaulis and Saxi- tings. -
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).