Acacia Cincinnata Fabaceae
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Volume 20: 29–33 ELOPEA Publication date: 16 February 2017 T dx.doi.org/10.7751/telopea11338 Journal of Plant Systematics plantnet.rbgsyd.nsw.gov.au/Telopea • escholarship.usyd.edu.au/journals/index.php/TEL • ISSN 0312-9764 (Print) • ISSN 2200-4025 (Online) Lectotypification of Mimosa pubescens Vent. (Fabaceae, Mimosoideae) Phillip G Kodela and Peter G Wilson National Herbarium of New South Wales, The Royal Botanic Gardens & Domain Trust, Mrs Macquaries Rd, Sydney, NSW 2000, Australia. [email protected]; [email protected] Abstract A lectotype is here designated for Mimosa pubescens Vent., the basionym of the Australian species Acacia pubescens (Vent.) R.Br. Introduction Acacia pubescens (Vent.) R.Br. has a restricted distribution in the greater Sydney region of New South Wales (see Tame 1992, Tindale and Kodela 2001, Kodela and Harden 2002, Kodela 2016, OEH 2016), and is listed as a Vulnerable species (OEH 2016). The basionym of Acacia pubescens, Mimosa pubescens, was originally published by Étienne Ventenat in the first volume of his work Jardin de la Malmaison (Ventenat 1803) that celebrated the collection of interesting plants from around the world in cultivation at the home of the Empress Josephine. Lack (2004: 35) notes that the number of Australian plants described in this work was “remarkably high” considering that the continent was, at that time, still largely unknown. The detailed descriptions were accompanied by fine illustrations by the famous botanical artist Redouté. At the time of compilation of the Acacia treatment in the Flora of Australia, no type specimen had been located (Tindale and Kodela 2001) and it was later suggested that the species could have been lectotypified on the plate in the protologue (Fig. -
Risk Assessment Robinia Pseudoacacia L
Risk assessment Robinia pseudoacacia L. Naamloos-2 1 15-03-13 08:10 © Naturalis Biodiversity Center, Leiden March 2013 Naamloos-2 2 15-03-13 08:10 Risk assessment Robinia pseudoacacia L. E. Boer March 2012 Naamloos-2 1 15-03-13 08:10 Naamloos-2 2 15-03-13 08:10 Table of contents 1. Introduction — 5 2. Robinia pseudoacacia: description, ecology and history — 6 2.1. Description — 6 2.2. Ecology — 6 3. Risk assessment — 8 3.1. Entry — 8 3.2. Establishment — 8 3.3. Spread — 8 3.4. Endangered areas — 9 3.5. Impact — 10 3.5.1. Ecological impact — 10 3.5.2. Economic impact — 10 3.5.3. Social impact — 11 4. Risk management — 12 4.1. Prevention of deliberate planting — 12 4.2. Prevention of dispersal — 12 4.3. Eradication and control — 12 4.4. Conclusions — 13 5. References — 14 Annex 1 Risk assessment scores using the ISEIA protocol — 16 This report was commissioned by the Invasive Alien Species Team of the Netherlands Food and Consumer Product Safety Authority. Table of contents 3 Naamloos-2 3 15-03-13 08:10 4 Risk assessment Robinia pseudoacacia L. Naamloos-2 4 15-03-13 08:10 1. Introduction Exotic, invasive plant species have a negative impact on biodiversity, economy and/or public health. For this reason the Invasive Alien Species Team of the Netherlands Food and Consumer Product Safety Authority has requested a risk assessment for Robinia pseudoacacia. The current risk assessment will focus on the situation in the Netherlands and discuss the following subjects: • Probability of entry • Probability of establishment in the Netherlands • Probability of spread • Identification of endangered areas based on the results of the three previous subjects • Impact of Robinia pseudoacacia in respect to ecological, economical and public health aspects • Management options to eradicate the species • Management options to control further spread and reduce impact. -
ACACIA Miller, Gard
Flora of China 10: 55–59. 2010. 31. ACACIA Miller, Gard. Dict. Abr., ed. 4, [25]. 1754, nom. cons. 金合欢属 jin he huan shu Acaciella Britton & Rose; Racosperma Martius; Senegalia Rafinesque; Vachellia Wight & Arnott. Morphological characters and geographic distribution are the same as those of the tribe. The genus is treated here sensu lato, including the African, American, Asian, and Australian species. Acacia senegal (Linnaeus) Willdenow and A. nilotica (Linnaeus) Delile were treated in FRPS (39: 28, 30. 1988) but are not treated here because they are only rarely cultivated in China. 1a. Leaves reduced to phyllodes. 2a. Phyllodes 10–20 × 1.5–6 cm; inflorescence a spike ...................................................................................... 1. A. auriculiformis 2b. Phyllodes 6–10 × 0.4–1 cm; inflorescence a head ................................................................................................... 2. A. confusa 1b. Leaves bipinnate. 3a. Flowers in racemes or spikes. 4a. Trees armed; pinnae 10–30 pairs ....................................................................................................................... 7. A. catechu 4b. Shrubs unarmed; pinnae 5–15 pairs. 5a. Racemes 2–5 cm; midveins of leaflets close to upper margin ............................................................ 8. A. yunnanensis 5b. Racemes shorter than 2 cm; midveins of leaflets subcentral ........................................................................ 5. A. glauca 3b. Flowers in heads, then rearranged in panicles. 6a. -
MOUNT AMOS South Pacific Ocean
Refer to this map as: Wet Tropics Bioregion MOUNT AMOS 1:50 000 SERIES WTMAveg Vegetation Survey QUEENSLAND SHEET 7966-1 EDITION 1 3 13 14 15 16 17 18 19 20 21145°20' 22 23 24 25 26 27 28 29 330 145°25' 31 32 33 34 35 36 37 38 39 145°30' MOUNT COOK NATIONAL PARK 15°30' 15°30' 43 85 Dawson Reef 85 62 84 56 84 South 83 An nan R 83 54a ive 70e r 42a 70a 70e 54a 54a Osterland Reef 39a 54a 55a 54a 55a 64a 82 54a 54a Cowlishaw Reef 54a 55a 64a 39a 82 70a 70a 70e 54a 70a 70a 70e Esk 70e 70a 70a 59a 81 29b 3a 70e 26a 70a 39a 81 54a 135 68d 70e Mount McIntosh 26a 70a 70e Draper Patch 29b 29b 64a 55a 70e 70e 39a 29b 26a 82 54a 39a 68d 80 21a Grave Point 70e 70e 33a 54a 59a 39a 25c 54a 8280 ANNAN RIVER 68d 54a 68d59b 55a 21a 33a 64a Walker Bay 43 70e 54a R 29b 39a 26a 54a i 47e 59a v 59a 68d e 48a 39a 77 Pacific 70e r 39a 29b 26a 50a 79 59a 70a 70e 26a 68d 29b 26a 70a 26a 70e 54a 59a 79 42a 33a 26a 55a 55a 68d 42a 48a 59a 54a54a 54a 110 48a 33a 55a 68d68d 42a 47e 29b 39a 54a 68d 59a 70e 55a 39a 62a 39a 42a 191 68d 39a 29b 67c 3a 70a 62a 67c Walker Hill 68d 33a 55a 33a 33a 39a 33a 67c 59b 59b 26a 78 NATIONAL PARK 39a 50a 42a 33a 33a 62a 59a 33a 3a 33a 50a 59a 39a Walker Point 78 62a 42a 59a 48a 29b 39a 26a 68d 48a 48a 3a 33a 59a 39a 3a 57a 33a 59b 39a 33a 67c 3a 59a 67c 68d 67c 67c 59a42a 26a 59a 39a 33a 33a 67c 64a 67c 59a 33a 59b 50a 76 57a 48a 67c 26a 77 33a 62a 42a 38 67c 67c 33a 39a 48a 67c 33a 67c 50a 39a 68d 62a 39a 67c 57a 77 61c 33a 29b 48a 67c 57 33a 33a 67c 29b 68d 42a 67c 67c 67c 42a 33a 39a 67c 67c 15°35' 59a 42a 64a 15°35' 50a 48a 33a -
Albizia Zygia Fabaceae
Albizia zygia (DC.) Macbr. Fabaceae - Mimosoideae LOCAL NAMES Igbo (nyie avu); Swahili (nongo); Yoruba (ayin rela) BOTANIC DESCRIPTION Albizia zygia is a deciduous tree 9-30 m tall with a spreading crown and a graceful architectural form. Bole tall and clear, 240 cm in diameter. Bark grey and smooth. Young branchlets densely to very sparsely clothed with minute crisped puberulence, usually soon disappearing but sometimes persistent. Leaves pinnate, pinnae in 2-3 pairs and broadening towards the apex, obliquely rhombic or obovate with the distal pair largest, apex obtuse, 29- 72 by 16-43 mm, leaves are glabrous or nearly so. Flowers subsessile; pedicels and calyx puberulous, white or pink; staminal tube exserted for 10-18 mm beyond corolla. Fruit pod oblong, flat or somewhat transversely plicate, reddish-brown in colour, 10-18 cm by 2-4 cm glabrous or nearly so. The seeds of A. zygia are smaller (7.5-10 mm long and 6.5 to 8.5 mm wide) and flatter than either of the other Albizia, but have the characteristic round shape, with a slightly swollen center. The genus was named after Filippo del Albizzi, a Florentine nobleman who in 1749 introduced A. julibrissin into cultivation. BIOLOGY A hermaphroditic species flowering in January, February, March, August, and September. Fruits ripen in January, February, March, April, November, and December. This tree hybridizes with A. gummifera. Agroforestry Database 4.0 (Orwa et al.2009) Page 1 of 5 Albizia zygia (DC.) Macbr. Fabaceae - Mimosoideae ECOLOGY A light demanding pioneer species, it is rarely found in closed canopy forests dominated by Chlorophora regia and Ficus macrosperma. -
Acacia in THIS ISSUE Dacacia the Name Acacia Comes This Issue of Seed Notes from the Greek Acacia, Ace Will Cover the Genus Or Acis Meaning a Point Or Acacia
No. 9 Acacia IN THIS ISSUE DAcacia The name Acacia comes This issue of Seed Notes from the Greek acacia, ace will cover the genus or acis meaning a point or Acacia. thorn, or from acazo, to D Description sharpen, although this name applies more to African than D Geographic Australian species (Australian distribution and Acacia have no thorns or habitat larger prickles, unlike those D Reproductive biology that are native to Africa). D Seed collection Many species of Acacia, or wattles as they are commonly D Phyllodes and flowers of Acacia aprica. Photo – Andrew Crawford Seed quality called in Australia, are valuable assessment for a range of uses, in D Seed germination particular as garden plants. Description In Australia, Acacia (family is modified to form a leaf- D Recommended reading They are also used for amenity plantings, windbreaks, shade DMimosaceae) are woody like structure or phyllode. trees, groundcovers, erosion plants that range from These phyllodes may be flat and salinity control. The timber prostrate under-shrubs to or terete. Some species do of some Acacia is very hard tall trees. Acacia flowers are not have phyllodes and the and is ideal for fence posts small, regular and usually flattened stems or cladodes (e.g. A. saligna or jam). Other bisexual. They occur in spikes act as leaves. Foliage can Acacia species are used to or in globular heads and vary from blueish to dark make furniture and ornaments. range in colour from cream green to silvery grey. Most The seed of some wattles is to intense yellow. The leaves species of Acacia have glands a good food source for birds, of Acacia may be bipinnate on the axis of the phyllodes, other animals and humans (the primary leaflets being although in Australian as ‘bush tucker’. -
Acacia Koa Fabaceae
Acacia koa Gray Fabaceae - Mimosoideae koa LOCAL NAMES English (koa acacia,koa,Hawaiian mahogany); Hawaian (koa); Trade name (koa) BOTANIC DESCRIPTION Acacia koa is a large, evergreen tree to 25 m tall, stem diameter to 150 cm at breast height. Trees occurring in dense, wet native forest stands typically retain a straight, narrow form. In the open, trees develop more spreading, branching crowns and shorter, broader trunks. A. koa has one main tap root and an otherwise shallow, spreading root system. Bark gray, Exclosure at Pohakuokala Gulch, Maui, rough, scaly and thick. Hawaii (Forest and Kim Starr) A. koa belongs to the thorn-less, phyllodinous group of the Acacia subgenus Heterophyllum. Young seedlings have bipinnate compound true leaves with 12-15 pairs of leaflets. Where forest light is sufficient, seedlings stop producing true leaves while they are less than 2 m tall. True leaves are retained longer by trees growing in dense shade. Phyllodes are sickle-shaped and often more than 2.5 cm wide in the middle and blunt pointed on each end. Inflorescence is a pale yellow ball, 8.5 mm in diameter, 1-3 on a common stalk. Each inflorescence is composed of many bisexual flowers. Each Habit at Makawao forest reserve, Maui, flower has an indefinite number of stamens and a single elongated style. Hawaii (Forest and Kim Starr) Pods are slow to dehisce, 15 cm long and 2.5-4 cm wide. They contain 6- 12 seeds that vary from dark brown to black. The generic name ‘acacia’ comes from the Greek word ‘akis’, meaning point or barb. -
Albizia Julibrissin Durazz
Albizia julibrissin Durazz. Fabaceae - Mimosoideae LOCAL NAMES Chinese (ho hun,ho huan); Dutch (acacia van Constantinopel); English (pink siris,Persian acacia,pink silk tree,mimosa,silk mimosa tree,silk tree,silky acacia,pink mimosa); French (arbre à soie,acacie de Constantinople); German (persische Seidenakazie,Julibrissin- Albizzie); Hindi (karmaru,brind,lal,tandai,shishi,sirin,siris,kurmru); Italian (acacia di Constantinopoli,gaggia di Constaninopoli,gaggia arborea,albero de la seta); Japanese (nemu-no-ki); Nepali (kato siris) BOTANIC DESCRIPTION Bark (James H. Miller, USDA Forest Albizia julibrissin is a small to medium-sized tree 6-9 m tall with a Service, www.forestryimages.org) spreading crown. The bark is light brown, nearly smooth, and generally thin with lens shaped areas along the stem. Leaves large, up to 50 cm long, bipinnately compound with 10-35 pairs of leaflets, many oblong leaflets, each only 6-12 mm long by about 7.5-10 cm wide, and alternate along the stems. Leaves fold up under the night sky Flowers showy, fragrant pink, about 3.75 cm long, that resembling pompoms and are arranged in panicles at the ends of branches. Fruits are flat, straw-colored pods about 15 cm long containing light brown Quick growing, flat-topped crown. Branches oval-shaped seeds about 1.25 cm in length. in lateral tiers. Long feathery fern-like leaves up to 45cm long - provide light shade. Spectacular in flower - from early summer to The generic name commemorates the Florentine nobleman Filippo degli autumn. Ornamental used as avenue tree Albizzi, who introduced the plant into cultivation in the middle of the 18th and lawn shade. -
Albizia Lophantha (Willd.) Benth, PLUME ALBIZIA, PLUME ACACIA
Albizia lophantha (Willd.) Benth, PLUME ALBIZIA, PLUME ACACIA. Small tree, evergreen, unarmed, 1-trunked, in range to 8 m tall; main branches horizontal, with widely spaced leaves; trunk < 12 cm diameter; bark fibrous and tough, grayish brown, brownish below wax, dull, transversely wrinkled, weakly ridged with smooth longitudinally veins and finer wrinkles. Stems: ridged, somewhat zigzagged, streaked olive green and rosy brown and becoming dark purple on ridges, internodes mostly 50–70 mm long, canescent. Leaves: helically alternate, even-2-pinnately compound with 7–13(–15) pairs of primary leaflets, petiolate, with stipules; stipules 2, attached to stem, acuminate and scalelike, hairy, persistent; petiole typically 30–60 mm long, with a conspicuous pulvinus at base and an extrafloral nectary at midpoint, the nectary oval, ± 3 mm long, green; blade oblong to chevron-rectangular in outline, 180–210 × 110–140 mm, with primary leaflets spreading or ascending, spaced 9−14 mm apart along rachis; rachis strongly ridged, with canescent hairs and erect, reddish glandular hairs, primary leaflets lacking stipel and having an extrafloral nectary at junction of the terminal pair of primary leaflets and sometimes another nectary at junction of penultimate pair of primary leaflets; petiolules with conspicuous pulvinus, having an upper pair of minute appendages at tip; primary leaflets often diverging at about 30−60°, 50–120 mm long, symmetric in length but lower leaflet length < terminal < middle leaflet length, with 25–40 pairs of secondary leaflets along axis; secondary leaflets with sleep movements, overlapping, asymmetrically oblong to elliptic, 3.5–8 × 1–2 mm, oblique at base, entire, broadly acute at tip, pinnately veined, upper surface glabrous, lower surface strigose and glaucous. -
The Following Tree Seedlings Are Available to Order from the State of Hawaii Division of Forestry and Wildlife, State Tree Nursery
The following tree seedlings are available to order from the State of Hawaii Division of Forestry and Wildlife, State Tree Nursery: Scientific Name: Common Name: Dibble/ Pot size: Acacia koa……………………… Koa……………………………….. Small Acacia koaia……………………... Koai’a……………………………. Small Araucaria columnaris…………….. Norfolk-island Pine……………… Small Cryptomeria japonica……………. Sugi Pine………………………… Small Cupressus lusitanica……………... Mexican Cypress………………… Small Cupressus macrocarpa…………… Monterey Cypress……………….. Small Cupressus simpervirens………….. Italian Cypress…………………… Medium Eucalyptus deglupta……………… Rainbow Bark……………………. Small Eucalyptus robusta……………….. Swamp Mahogany……………….. Small Metrosideros polymorpha……….. Ohia……………………………… Medium or 3” pot Pinus elliotii……………………… Slash Pine………………………... Small Pinus radiata……………………... Monterey Pine…………………… Small Podocarpus sp……………………. Podocarpus………………………. 3” pot Santalum sp……………………… Sandalwood……………………… Medium or 3” pot Tristania conferta………………… Brush Box………………………... Small Acacia koa (Koa): This large hardwood tree is endemic to the Hawaiian Islands. The tree has exceeded 100 ft in height with basal diameter far beyond 50 inches in old growth stands. The wood is prized for furniture and canoe works. This legume has pods with black seeds for reproduction. The wood has similar properties to that of black walnut. The yellow flowers are borne in dense round heads about 2@ in diameter. Tree growth is best above 800 ft; seems to grow best in the ‘Koa belt’ which is situated at an elevation range between 3,500 - 6,000 ft. It is often found in areas where there is fog in the late afternoons. It should be planted in well- drained fertile soils. Grazing animals relish the Koa foliage, so young seedlings should be protected Acacia koaia (Koaia): Related to the Koa, Koaia is native to Hawaii. The leaves and flowers are much the same as Koa. -
Synoptic Overview of Exotic Acacia, Senegalia and Vachellia (Caesalpinioideae, Mimosoid Clade, Fabaceae) in Egypt
plants Article Synoptic Overview of Exotic Acacia, Senegalia and Vachellia (Caesalpinioideae, Mimosoid Clade, Fabaceae) in Egypt Rania A. Hassan * and Rim S. Hamdy Botany and Microbiology Department, Faculty of Science, Cairo University, Giza 12613, Egypt; [email protected] * Correspondence: [email protected] Abstract: For the first time, an updated checklist of Acacia, Senegalia and Vachellia species in Egypt is provided, focusing on the exotic species. Taking into consideration the retypification of genus Acacia ratified at the Melbourne International Botanical Congress (IBC, 2011), a process of reclassification has taken place worldwide in recent years. The review of Acacia and its segregates in Egypt became necessary in light of the available information cited in classical works during the last century. In Egypt, various taxa formerly placed in Acacia s.l., have been transferred to Acacia s.s., Acaciella, Senegalia, Parasenegalia and Vachellia. The present study is a contribution towards clarifying the nomenclatural status of all recorded species of Acacia and its segregate genera. This study recorded 144 taxa (125 species and 19 infraspecific taxa). Only 14 taxa (four species and 10 infraspecific taxa) are indigenous to Egypt (included now under Senegalia and Vachellia). The other 130 taxa had been introduced to Egypt during the last century. Out of the 130 taxa, 79 taxa have been recorded in literature. The focus of this study is the remaining 51 exotic taxa that have been traced as living species in Egyptian gardens or as herbarium specimens in Egyptian herbaria. The studied exotic taxa are accommodated under Acacia s.s. (24 taxa), Senegalia (14 taxa) and Vachellia (13 taxa). -
Pleistocene Fossil Leaflets of Albizia Kalkora
Jpn. J. Histor. Bot. Vol. 26 No. 1 p. 3–13 February 2017 植生史研究 Original article Ayano Ito1, Arata Momohara2* and Zhekun Zhou3: Pleistocene fossil leafets of Albizia kalkora (Roxb.) Prain (Leguminosae subfamily Mimosoideae) from central Honshu, Japan, and its implications for historical biogeography 伊藤彩乃 1・百原 新 2*・周 浙昆 3: オオバネムノキ Albizia kalkora (Roxb.) Prain(マメ科ネムノキ亜科)の 本州中部更新統産小葉化石と,その歴史生物地理学的意味 Abstract Albizia kalkora (Leguminosae subfam. Mimosoideae) is a deciduous tree distributed in Japan, China, Korea, and other countries from Southeast Asia to India. In Japan, its distribution is restricted to the evergreen broadleaved forest zone in southern Kyushu, whereas it is widely distributed in the deciduous broadleaved for- est zone in China. Fossil records of A. kalkora from the Plio-Pleistocene have been limited in Kyushu, although A. miokalkora, a closely related fossil taxon, from the Miocene has been found in China, Korea, and Japan. We describe herein A. kalkora leafet fossils from the Lower Pleistocene Sayama Formation and Middle Pleistocene Shoudai Formation in central Japan. We compared the leafets with those of modern species in China with simi- lar morphology and identifed them as those of A. kalkora based on their size (2–3 cm long), the medial and base asymmetry, and the presence of 2–3 slender secondary veins diverging at the base. Their association with ever- green broadleaved trees in fossil assemblages indicates that A. kalkora expanded its distribution to central Japan during stages with warm winter temperatures. Its distribution was limited to southern Kyushu during the Late Quaternary in Japan, whereas in China it expanded widely into the deciduous broadleaved forest zone, possibly by adapting to cold winter conditions during glacial stages.