Walnut Jardin Botanique´ – Montreal, Quebec
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Natural Colourants with Ancient Concept and Probable Uses
JOURNAL OF ADVANCED BOTANY AND ZOOLOGY Journal homepage: http://scienceq.org/Journals/JABZ.php Review Open Access Natural Colourants With Ancient Concept and Probable Uses Tabassum Khair1, Sujoy Bhusan2, Koushik Choudhury2, Ratna Choudhury3, Manabendra Debnath4 and Biplab De2* 1 Department of Pharmaceutical Sciences, Assam University, Silchar, Assam, India. 2 Regional Institute of Pharmaceutical Science And Technology, Abhoynagar, Agartala, Tripura, India. 3 Rajnagar H. S. School, Agartala, Tripura, India. 4 Department of Human Physiology, Swami Vivekananda Mahavidyalaya, Mohanpur, Tripura, India. *Corresponding author: Biplab De, E-mail: [email protected] Received: February 20, 2017, Accepted: April 15, 2017, Published: April 15, 2017. ABSTRACT: The majority of natural colourants are of vegetable origin from plant sources –roots, berries, barks, leaves, wood and other organic sources such as fungi and lichens. In the medicinal and food products apart from active constituents there are several other ingredients present which are used for either ethical or technical reasons. Colouring agent is one of them, known as excipients. The discovery of man-made synthetic dye in the mid-19th century triggered a long decline in the large-scale market for natural dyes as practiced by the villagers and tribes. The continuous use of synthetic colours in textile and food industry has been found to be detrimental to human health, also leading to environmental degradation. Biocolours are extracted by the villagers and certain tribes from natural herbs, plants as leaves, fruits (rind or seeds), flowers (petals, stamens), bark or roots, minerals such as prussian blue, red ochre & ultramarine blue and are also of insect origin such as lac, cochineal and kermes. -
Juglans Nigra Juglandaceae L
Juglans nigra L. Juglandaceae LOCAL NAMES English (walnut,American walnut,eastern black walnut,black walnut); French (noyer noir); German (schwarze Walnuß); Portuguese (nogueira- preta); Spanish (nogal negro,nogal Americano) BOTANIC DESCRIPTION Black walnut is a deciduous tree that grows to a height of 46 m but ordinarily grows to around 25 m and up to 102 cm dbh. Black walnut develops a long, smooth trunk and a small rounded crown. In the open, the trunk forks low with a few ascending and spreading coarse branches. (Robert H. Mohlenbrock. USDA NRCS. The root system usually consists of a deep taproot and several wide- 1995. Northeast wetland flora: Field office spreading lateral roots. guide to plant species) Leaves alternate, pinnately compound, 30-70 cm long, up to 23 leaflets, leaflets are up to 13 cm long, serrated, dark green with a yellow fall colour in autumn and emits a pleasant sweet though resinous smell when crushed or bruised. Flowers monoecious, male flowers catkins, small scaley, cone-like buds; female flowers up to 8-flowered spikes. Fruit a drupe-like nut surrounded by a fleshy, indehiscent exocarp. The nut has a rough, furrowed, hard shell that protects the edible seed. Fruits Bark (Robert H. Mohlenbrock. USDA NRCS. 1995. Northeast wetland flora: Field office produced in clusters of 2-3 and borne on the terminals of the current guide to plant species) season's growth. The seed is sweet, oily and high in protein. The bitter tasting bark on young trees is dark and scaly becoming darker with rounded intersecting ridges on maturity. BIOLOGY Flowers begin to appear mid-April in the south and progressively later until early June in the northern part of the natural range. -
Juglans Spp., Juglone and Allelopathy
AllelopathyJournatT(l) l-55 (2000) O Inrernationa,^,,r,':'r::;:';::::,:rt;SS Juglansspp., juglone and allelopathy R.J.WILLIS Schoolof Botany.L.iniversity of Melbourre,Parkville, Victoria 3052, ALrstr.alia (Receivedin revisedform : February 26.1999) CONTENTS 1. Introduction 2. HistoricalBackground 3. The Effectsof walnutson otherplants 3.i. Juglansnigra 3.1.1.Effects on cropplants 3. I .2. Eft'ectson co-plantedtrees 3. 1 .3 . Effectson naturalvegetation 3.2. Juglansregia 3.2.1. Effectson otherplalrts 3.2.2.Effects on phytoplankton 1.3. Othel walnuts : Juglans'cinerea, J. ntttlor.J. mandshw-icu 4. Juglone 5. Variability in the effect of walnut 5.1. Intraspecificand Interspecific variation 5.2. Seasonalvariation 5.3 Variation in the effect of Juglansnigra on other.plants 5.4. Soil effects 6. Discussion Ke1'rvords: Allelopathy,crops, history, Juglan.s spp., juglone. phytoplankton,walnut, soil, TTCCS 1. INTRODUCTION The"rvalnuts" are referable to Juglans,a genusof 20-25species with a naturaldistribution acrossthe Northern Hemisphere and extending into SouthAmerica. Juglans is a memberof thefamily Juglandaceae which contains6 or 7 additionalgenera including Cruv,a, Cryptocctrva and a total of about 60 species. Walnuts are corrunerciallyimportant as the sourceof the ediblewalnut, the highly prizedtimber and as a specimentrees. Eating walnutsare usually obtarnedfrom -/. regia (the colrunonor Persianwalnut, erroneousll'known as the English walnut)- a nativeof SEEurope and Asia, which haslong been cultivated, but arealso sometin.res availablelocally from other speciessuch as J. nigra (back walnut) - a native of eastern North America andJ. ntajor, J. calfornica andJ. hindsii, native to the u,esternu.S. ILillis Grafting of supcrior fnrit-bearing scions of J. regia onlo rootstocksof hlrdier spccics. -
Black Walnut Juglans Nigra
black walnut Juglans nigra Kingdom: Plantae FEATURES Division: Magnoliophyta The deciduous black walnut tree may grow to a Class: Magnoliopsida height of 150 feet and a diameter of five feet. The Order: Fagales trunk is straight, and the crown is rounded. The bark is thick, black and deeply furrowed. The pith in the Family: Juglandaceae twigs is chambered, that is, divided by partitions. ILLINOIS STATUS The bud is rounded at the tip, pale brown and hairy. The pinnately compound leaves have 15 to 23 common, native leaflets and are arranged alternately on the stem. © Guy Sternberg Each lance-shaped leaflet may be up to three and one-half inches long and one and one-half inches wide. The leaflet is toothed along the edges, yellow- green and smooth above and paler and hairy below. Leaves turn yellow in the fall. Male and female flowers are separate but located on the same tree. The male (staminate) flowers are arranged in yellow- green, hairy catkins, while the female (pistillate) flowers are in small spikes. Neither type of flower has petals. The spherical fruits are arranged in groups of one or two. Each green or yellow-green walnut may be up to two inches in diameter. The husk on the fruit is thick, while the nut is very hard, oval, dark brown and deeply ridged. The seed is sweet to the taste. tree in summer BEHAVIORS The black walnut may be found statewide in Illinois. ILLINOIS RANGE This tree grows in rich woodlands. The black walnut flowers in April and May when the leaves are partly grown. -
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. -
Identification of Butternuts and Butternut Hybrids
Purdue University Purdue extension FNR-420-W & Natural Re ry sou Forestry and Natural Resources st rc re e o s F Identification of Butternuts and Butternut Hybrids Lenny Farlee1,3, Keith Woeste1, Michael Ostry2, James McKenna1 and Sally Weeks3 1 USDA Forest Service Hardwood Tree Improvement and Regeneration Center, Purdue University, 715 W. State Street, West Lafayette, IN, 47907 PURDUE UNIVERSITY 2 USDA Forest Service Northern Research Station, 1561 Lindig Ave. St. Paul, MN 55108 3 Department of Forestry and Natural Resources, Purdue University, 715 W. State Street, West Lafayette, IN, 47907 Introduction Butternut (Juglans cinerea), also known as white walnut, is a native hardwood related to black walnut (Juglans nigra) and other members of the walnut family. Butternut is a medium-sized tree with alternate, pinnately compound leaves that bears large, sharply ridged and corrugated, elongated, cylindrical nuts born inside sticky green hulls that earned it the nickname lemon-nut (Rink, 1990). The nuts are a preferred food of squirrels and other wildlife. Butternuts were collected and eaten by Native Americans (Waugh, 1916; Hamel and Chiltoskey, 1975) and early settlers, who also valued butternut for its workable, medium brown-colored wood (Kellogg, 1919), and as a source of medicine (Johnson, 1884), dyes (Hamel and Chiltoskey, 1975), and sap sugar. Butternut’s native range extends over the entire north- eastern quarter of the United States, including many states immediately west of the Mississippi River, and into Canada. Butternut is more cold-tolerant than black walnut, and it grows as far north as the Upper Peninsula of Michigan, New Brunswick, southern Quebec, and Figure 1. -
Texas Big Tree Registry a List of the Largest Trees in Texas Sponsored by Texas a & M Forest Service
Texas Big Tree Registry A list of the largest trees in Texas Sponsored by Texas A & M Forest Service Native and Naturalized Species of Texas: 320 ( D indicates species naturalized to Texas) Common Name (also known as) Latin Name Remarks Cir. Threshold acacia, Berlandier (guajillo) Senegalia berlandieri Considered a shrub by B. Simpson 18'' or 1.5 ' acacia, blackbrush Vachellia rigidula Considered a shrub by Simpson 12'' or 1.0 ' acacia, Gregg (catclaw acacia, Gregg catclaw) Senegalia greggii var. greggii Was named A. greggii 55'' or 4.6 ' acacia, Roemer (roundflower catclaw) Senegalia roemeriana 18'' or 1.5 ' acacia, sweet (huisache) Vachellia farnesiana 100'' or 8.3 ' acacia, twisted (huisachillo) Vachellia bravoensis Was named 'A. tortuosa' 9'' or 0.8 ' acacia, Wright (Wright catclaw) Senegalia greggii var. wrightii Was named 'A. wrightii' 70'' or 5.8 ' D ailanthus (tree-of-heaven) Ailanthus altissima 120'' or 10.0 ' alder, hazel Alnus serrulata 18'' or 1.5 ' allthorn (crown-of-thorns) Koeberlinia spinosa Considered a shrub by Simpson 18'' or 1.5 ' anacahuita (anacahuite, Mexican olive) Cordia boissieri 60'' or 5.0 ' anacua (anaqua, knockaway) Ehretia anacua 120'' or 10.0 ' ash, Carolina Fraxinus caroliniana 90'' or 7.5 ' ash, Chihuahuan Fraxinus papillosa 12'' or 1.0 ' ash, fragrant Fraxinus cuspidata 18'' or 1.5 ' ash, green Fraxinus pennsylvanica 120'' or 10.0 ' ash, Gregg (littleleaf ash) Fraxinus greggii 12'' or 1.0 ' ash, Mexican (Berlandier ash) Fraxinus berlandieriana Was named 'F. berlandierana' 120'' or 10.0 ' ash, Texas Fraxinus texensis 60'' or 5.0 ' ash, velvet (Arizona ash) Fraxinus velutina 120'' or 10.0 ' ash, white Fraxinus americana 100'' or 8.3 ' aspen, quaking Populus tremuloides 25'' or 2.1 ' baccharis, eastern (groundseltree) Baccharis halimifolia Considered a shrub by Simpson 12'' or 1.0 ' baldcypress (bald cypress) Taxodium distichum Was named 'T. -
Diversity of Wisconsin Rosids
Diversity of Wisconsin Rosids . oaks, birches, evening primroses . a major group of the woody plants (trees/shrubs) present at your sites The Wind Pollinated Trees • Alternate leaved tree families • Wind pollinated with ament/catkin inflorescences • Nut fruits = 1 seeded, unilocular, indehiscent (example - acorn) *Juglandaceae - walnut family Well known family containing walnuts, hickories, and pecans Only 7 genera and ca. 50 species worldwide, with only 2 genera and 4 species in Wisconsin Carya ovata Juglans cinera shagbark hickory Butternut, white walnut *Juglandaceae - walnut family Leaves pinnately compound, alternate (walnuts have smallest leaflets at tip) Leaves often aromatic from resinous peltate glands; allelopathic to other plants Carya ovata Juglans cinera shagbark hickory Butternut, white walnut *Juglandaceae - walnut family The chambered pith in center of young stems in Juglans (walnuts) separates it from un- chambered pith in Carya (hickories) Juglans regia English walnut *Juglandaceae - walnut family Trees are monoecious Wind pollinated Female flower Male inflorescence Juglans nigra Black walnut *Juglandaceae - walnut family Male flowers apetalous and arranged in pendulous (drooping) catkins or aments on last year’s woody growth Calyx small; each flower with a bract CA 3-6 CO 0 A 3-∞ G 0 Juglans cinera Butternut, white walnut *Juglandaceae - walnut family Female flowers apetalous and terminal Calyx cup-shaped and persistant; 2 stigma feathery; bracted CA (4) CO 0 A 0 G (2-3) Juglans cinera Juglans nigra Butternut, white -
Localized Gene Expression Changes During Adventitious Root Formation in Black Walnut (Juglans Nigra L.)
Tree Physiology 38, 877–894 doi:10.1093/treephys/tpx175 Research paper Localized gene expression changes during adventitious root formation in black walnut (Juglans nigra L.) Micah E. Stevens1, Keith E. Woeste2 and Paula M. Pijut2,3 1Department of Forestry and Natural Resources, Purdue University, Hardwood Tree Improvement and Regeneration Center (HTIRC), 715 West State Street, West Lafayette, IN 47907, USA; 2USDA Forest Service, Northern Research Station, HTIRC, 715 West State Street, West Lafayette, IN 47907, USA; 3Corresponding author ([email protected]) Received May 31, 2017; accepted December 20, 2017; published online January 25, 2018; handling Editor Danielle Way Cutting propagation plays a large role in the forestry and horticulture industries where superior genotypes need to be clonally multiplied. Integral to this process is the ability of cuttings to form adventitious roots. Recalcitrance to adventitious root develop- ment is a serious hurdle for many woody plant propagation systems including black walnut (Juglans nigra L.), an economically valuable species. The inability of black walnut to reliably form adventitious roots limits propagation of superior genotypes. Adventitious roots originate from different locations, and root induction is controlled by many environmental and endogenous factors. At the molecular level, however, the regulation of adventitious root formation is still poorly understood. In order to eluci- date the transcriptional changes during adventitious root development in black walnut, we used quantitative real-time polymer- ase chain reaction to measure the expression of nine key genes regulating root formation in other species. Using our previously developed spatially explicit timeline of adventitious root development in black walnut softwood cuttings, we optimized a laser capture microdissection protocol to isolate RNA from cortical, phloem fiber and phloem parenchyma cells throughout adventi- tious root formation. -
Analysis of Phylogenetic Relationships in the Walnut Family Based on Internal Transcribed Spacer Sequences and Secondary Structures(ITS2)
Analysis of Phylogenetic Relationships in The Walnut Family Based on Internal Transcribed Spacer Sequences and Secondary Structures(ITS2) Zhongzhong Guo Tarim University Qiang Jin Tarim University Zhenkun Zhao Tarim University Wenjun Yu Tarim University Gen Li Tarim University Yunjiang Cheng Tarim University Cuiyun Wu Tarim University rui Zhang ( [email protected] ) Tarim University https://orcid.org/0000-0002-4360-5179 Research Article Keywords: Base sequence, Evolution, Juglandaceae, Ribosomal spacer, Secondary structure Posted Date: May 13th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-501634/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/23 Abstract This study aims to investigate the phylogenetic relationships within the Juglandaceae family based on the Internal Transcribed Spacer's primary sequence and secondary structures (ITS2). Comparative analysis of 51 Juglandaceae species was performed across most of the dened seven genera. The results showed that the ITS2 secondary structure's folding pattern was highly conserved and congruent with the eukaryote model. Firstly, Neighbor-joining (N.J.) analysis recognized two subfamilies: Platycaryoideae and Engelhardioideae. The Platycaryoideae included the Platycaryeae (Platycarya+ (Carya+ Annamocarya)) and Juglandeae (Juglans-(Cyclocarya + Pterocarya)). The Engelhardioideae composed the (Engelhardia+Oreomunnea+Alfaroa)). The Rhoiptelea genus was generally regarded as an outgroup when inferring the phylogeny of Juglandaceae. However, it is clustered into the Juglandaceae family and showed a close relationship with the Platycaryoideae subfamily. Secondly, the folded 3-helices and 4-helices secondary structure of ITS2 were founded in the Juglandaceae family. Therefore, these ITS2 structures could be used as formal evidence to analyze Juglandaceae's phylogeny relationship. -
Reproduction and Potential Range Expansion of Walnut Twig Beetle Across the Juglandaceae
Biol Invasions (2018) 20:2141–2155 https://doi.org/10.1007/s10530-018-1692-5 ORIGINAL PAPER Reproduction and potential range expansion of walnut twig beetle across the Juglandaceae Andrea R. Hefty . Brian H. Aukema . Robert C. Venette . Mark V. Coggeshall . James R. McKenna . Steven J. Seybold Received: 10 June 2017 / Accepted: 19 February 2018 / Published online: 1 March 2018 Ó This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2018 Abstract Biological invasions by insects that vector this insect has expanded its geographic range by plant pathogens have altered the composition of colonizing naı¨ve hosts. The objective of this study was natural and urban forests. Thousand cankers disease to characterize limits to, and variation within, the host is a new, recent example and is caused by the complex range of P. juglandis and infer the extent to which of walnut twig beetle, Pityophthorus juglandis, and hosts might constrain the geographic distribution of the fungus, Geosmithia morbida, on susceptible hosts, the insect. We examined colonization and reproduc- notably some Juglans spp. and Pterocarya spp. Host tion by P. juglandis in no-choice laboratory experi- colonization by P. juglandis may be particularly ments with 11 Juglans spp., one Pterocarya sp., and important for disease development, but the beetle’s two Carya spp. over 2 years and found that all but the host range is not known. In the United States and Italy, Carya spp. were hosts. Reproduction was generally greater on Juglans californica, J. hindsii, and J. nigra, than on J. -
Plant Gems from China©
1 Plant Gems from China© Donghui Peng1, Longqing Chen2 and Mengmeng Gu3 1College of Landscape Architecture and Horticulture, Fujian Agriculture and Forestry University, Fuzhou, Fujian Province 350002, PRC 2College of Forestry and Horticulture, Huazhong Agriculture University, Wuhan, Hubei Province 430070, PRC 3Department of Horticultural Sciences, Texas A&M AgriLife Extension Service, College Station, TX 77843, USA Email: [email protected] INTRODUCTION A lot of plants native in China thrive in landscapes across the U.S. Chinese plant germplasm has been continuously introduced to the U.S., and used in breeding and selection. So many new cultivars with Chinese genetics have been introduced in the landscape plant market. The Chinese love plants and particularly enjoy ten “traditionally famous flowers”: lotus (Nelumbo nucifera), sweet olive (Osmanthus frangrans), peony (Paeonia suffruticosa), azalea (Azalea spp.), chrysanthemum (Chrysanthemum spp.), Mei flower (Prunus mume), daffodil (Narcissus spp.), rose (Rosa spp.), camellia (Camellia spp.) and cymbidium (Cymbidium spp.). Public and university breeders have focused on these taxa. In addition, many species and cultivars commonly grown in China may be of interest to growers and landscape professionals in the U.S, which this manuscript will be focused on. PLANT SPECIES AND CULTIVARS Sweet olive (Osmanthus fragrans). There are mainly four types of sweet olives, Auranticus Group, Luteus Group, Albus Group, orange and Semperflorens Group. Ever-blooming sweet 1 2 olives have peak blooming in the fall like the others, and continue for about six months although not as profusely. Recently there are three variegated cultivars: ‘Yinbian Caiye’ with white leaf margins mature leaves and red/white/green on new growth, ‘Yintian Cai’ with red-margined maroon leaves maturing to white-margined green leaves, and ‘Pearl Color’ with pink new growth.