Cybister Amaryllis Vegetative Matters
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Summary of Offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019
Summary of offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019 3841 Number of items in BX 301 thru BX 463 1815 Number of unique text strings used as taxa 990 Taxa offered as bulbs 1056 Taxa offered as seeds 308 Number of genera This does not include the SXs. Top 20 Most Oft Listed: BULBS Times listed SEEDS Times listed Oxalis obtusa 53 Zephyranthes primulina 20 Oxalis flava 36 Rhodophiala bifida 14 Oxalis hirta 25 Habranthus tubispathus 13 Oxalis bowiei 22 Moraea villosa 13 Ferraria crispa 20 Veltheimia bracteata 13 Oxalis sp. 20 Clivia miniata 12 Oxalis purpurea 18 Zephyranthes drummondii 12 Lachenalia mutabilis 17 Zephyranthes reginae 11 Moraea sp. 17 Amaryllis belladonna 10 Amaryllis belladonna 14 Calochortus venustus 10 Oxalis luteola 14 Zephyranthes fosteri 10 Albuca sp. 13 Calochortus luteus 9 Moraea villosa 13 Crinum bulbispermum 9 Oxalis caprina 13 Habranthus robustus 9 Oxalis imbricata 12 Haemanthus albiflos 9 Oxalis namaquana 12 Nerine bowdenii 9 Oxalis engleriana 11 Cyclamen graecum 8 Oxalis melanosticta 'Ken Aslet'11 Fritillaria affinis 8 Moraea ciliata 10 Habranthus brachyandrus 8 Oxalis commutata 10 Zephyranthes 'Pink Beauty' 8 Summary of offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019 Most taxa specify to species level. 34 taxa were listed as Genus sp. for bulbs 23 taxa were listed as Genus sp. for seeds 141 taxa were listed with quoted 'Variety' Top 20 Most often listed Genera BULBS SEEDS Genus N items BXs Genus N items BXs Oxalis 450 64 Zephyranthes 202 35 Lachenalia 125 47 Calochortus 94 15 Moraea 99 31 Moraea -
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
Differences in Floral Development Between Lycoris Radiata And
R ESEARCH ARTICLE doi: 10.2306/scienceasia1513-1874.2020.032 Differences in floral development between Lycoris radiata and Lycoris sprengeri a,† b,† c d a a,e, Junhuo Cai , Junjun Fan , Xuying Wei , Donglin Zhang , Jiajia Ren , Lu Zhang ∗ a College of Landscape and Art, Jiangxi Agricultural University, Nanchang 330045 China b College of Horticulture, Jinling Institute of Technology, Nanjing 210037 China c College of Art, Jiangxi Finance and Economics University, Nanchang 330032 China d Department of Horticulture, University of Georgia, Athens, GA 30602 USA e Collaboration Innovation Center of Jiangxi Typical Trees Cultivation and Utilization, Jiangxi Agricultural University, Nanchang 330045 China ∗Corresponding author, e-mail: [email protected], Cai J. and Fan J. contributed equally to this paper. Received 12 Sep 2019 Accepted 21 Mar 2020 ABSTRACT: Lycoris radiata and Lycoris sprengeri are two typical plants of the genus Lycoris. They have different leafing and flowering patterns. To understand the habits of Lycoris species and regulate the flowering period effectively, we compared flower bud development of these two species using phenological, anatomical, and physiological measurements. Our results showed there were significant differences in phenology between the two species. The sprouting stage of L. radiata took place in autumn, the leaf growth period lasted seven months, dormancy lasted approximately 100 days before flowering, and there was no dormancy period after flowering. In comparison, the sprouting period of L. sprengeri was delayed until the spring of the following year, the leaf growth stage lasted approximately 3 months, the flowering stage took place from Jul–Aug, and dormancy lasted 1–2 months before flowering and for another 6 months after flowering. -
Comparative Chloroplast Genomes of Four Lycoris Species (Amaryllidaceae) Provides New Insight Into Interspecific Relationship and Phylogeny
biology Article Comparative Chloroplast Genomes of Four Lycoris Species (Amaryllidaceae) Provides New Insight into Interspecific Relationship and Phylogeny Fengjiao Zhang 1,2, Ning Wang 1,2, Guanghao Cheng 1,2, Xiaochun Shu 1,2, Tao Wang 1,2 , Weibing Zhuang 1,2, Ruisen Lu 1,2,* and Zhong Wang 1,2,* 1 Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing 210014, China; [email protected] (F.Z.); [email protected] (N.W.); [email protected] (G.C.); [email protected] (X.S.); [email protected] (T.W.); [email protected] (W.Z.) 2 The Jiangsu Provincial Platform for Conservation and Utilization of Agricultural Germplasm, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing 210014, China * Correspondence: [email protected] (R.L.); [email protected] (Z.W.) Simple Summary: The genus Lycoris (Amaryllidaceae) comprises about 20 species with high orna- mental and medicinal value. However, germplasm identification is still difficult due to frequent interspecific hybridization and intraspecific morphological variation within this genus. Plastid genome sequencing has been proven to be a useful tool to identify closely related species and is widely used in the field of plant evolution and phylogeny. In the present study, we provided four Citation: Zhang, F.; Wang, N.; chloroplast genomes of Lycoris and retrieved seven published species in the genus for comparative Cheng, G.; Shu, X.; Wang, T.; Zhuang, genomics and phylogenetic analyses. All these chloroplast genomes possess the typical quadripartite W.; Lu, R.; Wang, Z. -
Complete Chloroplast Genomes Shed Light on Phylogenetic
www.nature.com/scientificreports OPEN Complete chloroplast genomes shed light on phylogenetic relationships, divergence time, and biogeography of Allioideae (Amaryllidaceae) Ju Namgung1,4, Hoang Dang Khoa Do1,2,4, Changkyun Kim1, Hyeok Jae Choi3 & Joo‑Hwan Kim1* Allioideae includes economically important bulb crops such as garlic, onion, leeks, and some ornamental plants in Amaryllidaceae. Here, we reported the complete chloroplast genome (cpDNA) sequences of 17 species of Allioideae, fve of Amaryllidoideae, and one of Agapanthoideae. These cpDNA sequences represent 80 protein‑coding, 30 tRNA, and four rRNA genes, and range from 151,808 to 159,998 bp in length. Loss and pseudogenization of multiple genes (i.e., rps2, infA, and rpl22) appear to have occurred multiple times during the evolution of Alloideae. Additionally, eight mutation hotspots, including rps15-ycf1, rps16-trnQ-UUG, petG-trnW-CCA , psbA upstream, rpl32- trnL-UAG , ycf1, rpl22, matK, and ndhF, were identifed in the studied Allium species. Additionally, we present the frst phylogenomic analysis among the four tribes of Allioideae based on 74 cpDNA coding regions of 21 species of Allioideae, fve species of Amaryllidoideae, one species of Agapanthoideae, and fve species representing selected members of Asparagales. Our molecular phylogenomic results strongly support the monophyly of Allioideae, which is sister to Amaryllioideae. Within Allioideae, Tulbaghieae was sister to Gilliesieae‑Leucocoryneae whereas Allieae was sister to the clade of Tulbaghieae‑ Gilliesieae‑Leucocoryneae. Molecular dating analyses revealed the crown age of Allioideae in the Eocene (40.1 mya) followed by diferentiation of Allieae in the early Miocene (21.3 mya). The split of Gilliesieae from Leucocoryneae was estimated at 16.5 mya. -
Sell Cut Flowers from Perennial Summer-Flowering Bulbs
SELL CUT FLOWERS FROM PERENNIAL SUMMER-FLOWERING BULBS Andy Hankins Extension Specialist-Alternative Agriculture, Virginia State University Reviewed by Chris Mullins, Virginia State University 2018 Commercial producers of field-grown flower cut flowers generally have a wide selection of crops to sell in April, May and June. Many species of annual and especially perennial cut flowers bloom during these three months. Many flower crops are sensitive to day length. Crops that bloom during long days such as larkspur, yarrow, peonies and gypsophila cannot be made to bloom after the summer equinox on June 21st. Other crops such as snapdragons may be day length neutral but they are adversely affected by the very warm days and nights of mid-summer. It is much more challenging for Virginia cut flower growers to have a diverse selection of flower crops for marketing from July to September when day length is getting shorter and day temperatures are getting hotter. Quite a few growers offer the same inventory of sunflowers, zinnias, celosia and gladiolas during the middle of the summer because everything else has come and gone. A group of plants that may offer new opportunities for sales of cut flowers during mid-summer are summer-flowering bulbs. Many of these summer-flowering bulbs are tropical plants that have only become available in the United States during the last few years. The first question that growers should ask about any tropical plant recommended for field planting is, " Will this species be winter hardy in Virginia?" Many of the bulb species described in this article are not very winter hardy. -
JUDD W.S. Et. Al. (1999) Plant Systematics
CHAPTER8 Phylogenetic Relationships of Angiosperms he angiosperms (or flowering plants) are the dominant group of land Tplants. The monophyly of this group is strongly supported, as dis- cussed in the previous chapter, and these plants are possibly sister (among extant seed plants) to the gnetopsids (Chase et al. 1993; Crane 1985; Donoghue and Doyle 1989; Doyle 1996; Doyle et al. 1994). The angio- sperms have a long fossil record, going back to the upper Jurassic and increasing in abundance as one moves through the Cretaceous (Beck 1973; Sun et al. 1998). The group probably originated during the Jurassic, more than 140 million years ago. Cladistic analyses based on morphology, rRNA, rbcL, and atpB sequences do not support the traditional division of angiosperms into monocots (plants with a single cotyledon, radicle aborting early in growth with the root system adventitious, stems with scattered vascular bundles and usually lacking secondary growth, leaves with parallel venation, flow- ers 3-merous, and pollen grains usually monosulcate) and dicots (plants with two cotyledons, radicle not aborting and giving rise to mature root system, stems with vascular bundles in a ring and often showing sec- ondary growth, leaves with a network of veins forming a pinnate to palmate pattern, flowers 4- or 5-merous, and pollen grains predominantly tricolpate or modifications thereof) (Chase et al. 1993; Doyle 1996; Doyle et al. 1994; Donoghue and Doyle 1989). In all published cladistic analyses the “dicots” form a paraphyletic complex, and features such as two cotyle- dons, a persistent radicle, stems with vascular bundles in a ring, secondary growth, and leaves with net venation are plesiomorphic within angio- sperms; that is, these features evolved earlier in the phylogenetic history of tracheophytes. -
Introducing Lycoris to U.S. Flower Lovers
PEGGY GREB (D300-1) Introducing Lycoris to Golden-yellow fl owers of Lycoris aurea. U.S. Flower Lovers or more than 20 years ARS horticulturist Mark Roh has been intrigued by the origins and habitats of the exotic and beautiful Lycoris. Though various Lycoris species have been grown as ornamentals in China, F Korea, and Japan for many centuries, only two species are readily available here: L. squamigera and L. radiata. They—and the rarer L. incarnata, L. chejuensis, and L. flavescens—are maintained at the U.S. National Arboretum (USNA), in Washington, D.C., and in Beltsville, Maryland. In 1984, Roh collected several unidentified Lycoris species from Anduck Valley, on Korea’s Jeju Island. This subtropical area hosts about 4,000 species of plants. Then in 1998, more Lycoris species were collected in Japan, Korea, and China. DNA molecular markers and chromosome studies proved that some of the unidentified Lycoris collected from Anduck Valley were L. incarnata, a species previously known to be native only to China. It is possible that this accession was brought from China to Korea by bulb collectors, but no record of that can be found. In the past 6 years, extensive visits to areas near Anduck Valley have been made by Roh or by collaborators Mun Seok Seong, of Jeju-do Agricultural Research and Extension Services, and Yong Bong Park, 12 Agricultural Research/December 2005 387664.indd 12 11/11/05 6:23:47 AM PEGGY GREB (D303-1) of Jeju National University. But they have of drought and waterlogging, as well as failed to locate any more L. -
Nerine Bowdenii Final Trials Report 2012–2017
Nerine bowdenii Final Trials Report 2012–2017 Trials Office, RHS Garden Wisley, Woking, Surrey, GU23 6QB RHS Registered Charity No: 222879 / SC038262 RHS Trial of Nerine bowdenii Introduction to the Trial The genus Nerine contains 25 species, most well known of which is the Guernsey lily (N. sarniensis) a greenhouse plant. All the species occur in southern Africa but only a very few are truly hardy in the UK. Since its introduction to cultivation in 1898 N. bowdenii has become widely grown in gardens and a diverse range of forms has been developed, either by selection or hybridisation. The scale of this diversity was revealed by the Hardy Nerine Study Day in October 2007. From that point onwards the idea of a trial grew, mainly through the efforts of the then National Plant Collection holder for hardy nerines, Mrs Margaret Owen. The trial agreed was an RHS off-site trial, run jointly by the RHS and the Nerine and Amaryllid Society (NAAS). Two sites were chosen to test the hardiness of the entries: one in the north (The Patch, Acton Pigott, Shropshire – site of the then National Plant Collection) and one in the south (Bramdean House, Bramdean, Hampshire – site of an extensive collection of nerines owned by Mrs Victoria Wakefield). Although the intention was to have entries in common to both sites to allow proper comparison, the difficult process of putting the trial together meant that not all the entries were grown at both sites. A particular challenge for the trial was the fact that many of the entries were not named or not properly named as cultivars. -
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Shichao Chen1., Dong-Kap Kim2., Mark W. Chase3, Joo-Hwan Kim4* 1 College of Life Science and Technology, Tongji University, Shanghai, China, 2 Division of Forest Resource Conservation, Korea National Arboretum, Pocheon, Gyeonggi- do, Korea, 3 Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, United Kingdom, 4 Department of Life Science, Gachon University, Seongnam, Gyeonggi-do, Korea Abstract Phylogenetic analysis aims to produce a bifurcating tree, which disregards conflicting signals and displays only those that are present in a large proportion of the data. However, any character (or tree) conflict in a dataset allows the exploration of support for various evolutionary hypotheses. Although data-display network approaches exist, biologists cannot easily and routinely use them to compute rooted phylogenetic networks on real datasets containing hundreds of taxa. Here, we constructed an original neighbour-net for a large dataset of Asparagales to highlight the aspects of the resulting network that will be important for interpreting phylogeny. The analyses were largely conducted with new data collected for the same loci as in previous studies, but from different species accessions and greater sampling in many cases than in published analyses. The network tree summarised the majority data pattern in the characters of plastid sequences before tree building, which largely confirmed the currently recognised phylogenetic relationships. Most conflicting signals are at the base of each group along the Asparagales backbone, which helps us to establish the expectancy and advance our understanding of some difficult taxa relationships and their phylogeny. -
Lesson 3 RECOGNISING PLANT FAMILIES and IDENTIFYING PLANTS Aim Distinguish Between Different Plant Families and to Become Profi
Lesson 3 RECOGNISING PLANT FAMILIES AND IDENTIFYING PLANTS Aim Distinguish between different plant families and to become proficient at identifying plants. The best way to build your ability to identify plants is by working with or handling a variety of different plants on a daily basis. The first ten plant names you learn are always much more difficult than the next ninety. Similarly, the first 100 names are always much more difficult than the next 900. If you plan to be a skilled gardener, landscape designer, or horticulturist: you need to learn to identify hundreds of different plants. As you have seen earlier; there is a system in identifying plant names. BECOME FAMILIAR WITH PLANT FAMILIES If you can get to know the way the system works, and the broad categories, the whole thing starts to make a great deal more sense. Each new name you confront is able to be associated with things and remembered more easily. FOR EXAMPLE: “When I see a plant with a daisy flower, I immediately know that it is in the Asteraceae family. Even if the genus is new to me, I will be more likely to remember it because I’m not only thinking: This is the genus of this new plant , but I am also thinking: This new genus is in the Asteraceae family. In essence, my brain is registering two pieces of information instead of one and that doubles the likelihood of me remembering the plant. BECOME FAMILIAR WITH LATIN Plant naming is based on the ancient Roman language of Latin. -
The Durable Lycoris Species and the Shared Variety Names
The Durable Lycoris Species and the Shared Variety Names By Joe Francis, Fairfax Master Gardener The genus Lycoris has 13 to 21 species all sharing the same growth characteristics: a dormancy period followed by a blooming cycle, vegetative regeneration and return to dormancy. Because their dormancy ends with the sudden emergence of a flower scape from a bare surface, these cultivars carry a common name, ‘Naked Ladies.’ Unfortunately, retail catalogs over time quite often mixed their presentation offerings without clear regard to their accurate species nomenclature and their proper cultural instructions. This article will focus on four species successfully photo: Joe Francis grown in the Mid-Atlantic region, arranged by Lycoris squamigera within hydrangea their approximate blooming time: the pink Lycoris squamigera, the electric blue Lycoris sprengeri, the red Lycoris radiata and the yellow Lycoris aurea. Lycoris squamigera In the mid-20th century, gardeners were taught that Lycoris squamigera [common names: Resurrection lily, Magic lily and Naked Lady lily] heralded from Japan was a reliable low maintenance perennial bulb. It makes its vegetative appearance of dense strap leaves in late January. One can expect to see this lush green growth over time join the spring flowering bulb crowd, and then with the greatest amount of discretion fade its winter growth and make way for the spring flowering perennials. It lapses into dormancy during the late spring through the hot parts of the summer. Its period of dormancy is tied to the sun’s descent from its apex beginning in late June. As the angle of the sun changes, so does the soil temperature pattern.