Croatia & Slovenia – Spring in Istria
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Catalogue2013 Web.Pdf
bwfp British Wild Flower Plants www.wildflowers.co.uk Plants for Trade Plants for Home Specialist Species Wildflower Seed Green Roof Plants Over 350 species Scan here to of British native buy online plants 25th Anniversary Year Finding Us British Wild Flower Plants Burlingham Gardens 31 Main Road North Burlingham Norfolk NR13 4TA Phone / Fax: (01603) 716615 Email: [email protected] Website: http://www.wildflowers.co.uk Twitter: @WildflowersUK Nursery Opening Times Monday to Thursday: 10.00am - 4.00pm Friday: 10.00am - 2.30pm Please note that we are no longer open at weekends or Bank Holidays. Catalogue Contents Contact & Contents Page 02 About Us Page 03 Mixed Trays Pages 04-05 Reed Beds Page 06 Green Roofs Page 07 Wildflower Seeds Page 08 Planting Guide Pages 09-10 Attracting Wildlife Page 11 Rabbit-Proof Plants Page 12 List of Plants Pages 13-50 Scientific Name Look Up Pages 51-58 Terms & Conditions Page 59 www.wildflowers.co.uk 2 Tel/Fax:(01603)716615 About Us Welcome.... About Our Plants We are a family-run nursery, situated in Norfolk on a Our species are available most of the year in: six acre site. We currently stock over 350 species of 3 native plants and supply to all sectors of the industry Plugs: Young plants in 55cm cells with good rootstock. on a trade and retail basis. We are the largest grower of native plants in the UK and possibly Europe. Provenance Our species are drawn from either our own seed collections or from known provenance native sources. We comply with the Flora Locale Code of Practice. -
Morphological Systematics of Serapias L.(Orchidaceae) in Southwest
Pl. Syst. Evol. 265: 165–177 (2007) Plant Systematics DOI 10.1007/s00606-007-0519-0 and Evolution Printed in The Netherlands Morphological systematics of Serapias L. (Orchidaceae) in Southwest Europe C. Venhuis, P. Venhuis, J. G. B. Oostermeijer, and P. H. van Tienderen Institute for Biodiversity and Ecosystem Dynamics, Universiteit van Amsterdam, Amsterdam, The Netherlands Received January 27, 2006; accepted January 18, 2007 Published online: April 30, 2007 Ó Springer-Verlag 2007 Abstract. We measured morphological characters while Sundermann (1980) only mentioned and relative DNA contents to assess variation and three. The distribution is predominantly Med- phylogenetic relationships among Serapias species in iterranean. Its range extends from the Azores three populations of each of the 10 putative taxa that and the Canaries in the west to the Caucasus in occur in Southwest Europe. DNA contents indicated the east, and as far north as Brittany (France) diploidy for most species, except for tetraploid S. (Go¨lz and Reinhard 1980; Perez Chiscano lingua and hexaploid S. olbia. Multivariate (discrimi- et al. 1991; Delforge 1995, 2002). The genus nant) analyses yielded two main groups: a small- flowered S. parviflora group and a large-flowered is considered monophyletic, based on genetic S. vomeracea group. Within the S. parviflora group, S. (Pridgeon et al. 1997; Bateman et al. 1997, elsae should be considered a large-flowered variation 2003) and morphological differences (Delforge of S. strictiflora. The geographically disjunct S. gre- 1995, 2002). Serapias is represented in south- garia and S. strictiflora are probably different taxa. In west Europe (Iberian Peninsula and southern the S. -
State of New York City's Plants 2018
STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species. -
Breeding System Diversification and Evolution in American Poa Supersect. Homalopoa (Poaceae: Poeae: Poinae)
Annals of Botany Page 1 of 23 doi:10.1093/aob/mcw108, available online at www.aob.oxfordjournals.org Breeding system diversification and evolution in American Poa supersect. Homalopoa (Poaceae: Poeae: Poinae) Liliana M. Giussani1,*, Lynn J. Gillespie2, M. Amalia Scataglini1,Marıa A. Negritto3, Ana M. Anton4 and Robert J. Soreng5 1Instituto de Botanica Darwinion, San Isidro, Buenos Aires, Argentina, 2Research and Collections Division, Canadian Museum of Nature, Ottawa, Ontario, Canada, 3Universidad de Magdalena, Santa Marta, Colombia, 4Instituto Multidisciplinario de Biologıa Vegetal (IMBIV), CONICET-UNC, Cordoba, Argentina and 5Department of Botany, Smithsonian Institution, Washington, DC, USA *For correspondence. E-mail [email protected] Received: 11 December 2015 Returned for revision: 18 February 2016 Accepted: 18 March 2016 Downloaded from Background and Aims Poa subgenus Poa supersect. Homalopoa has diversified extensively in the Americas. Over half of the species in the supersection are diclinous; most of these are from the New World, while a few are from South-East Asia. Diclinism in Homalopoa can be divided into three main types: gynomonoecism, gynodioe- cism and dioecism. Here the sampling of species of New World Homalopoa is expanded to date its origin and diver- sification in North and South America and examine the evolution and origin of the breeding system diversity. Methods A total of 124 specimens were included in the matrix, of which 89 are species of Poa supersect. http://aob.oxfordjournals.org/ Homalopoa sections Acutifoliae, Anthochloa, Brizoides, Dasypoa, Dioicopoa, Dissanthelium, Homalopoa sensu lato (s.l.), Madropoa and Tovarochloa, and the informal Punapoa group. Bayesian and parsimony analyses were conducted on the data sets based on four markers: the nuclear ribosomal internal tanscribed spacer (ITS) and exter- nal transcribed spacer (ETS), and plastid trnT-L and trnL-F. -
Pdf of JHOS July 2013
JJoouurrnnaall of the HHAARRDDYY OORRCCHHIIDD SSOOCCIIEETTYY Vol. 10 No. 3 (699) July 2013 JOURNAL of the HARDY ORCHID SOCIETY Vol. 10 No. 3 (69) July 2013 The Hardy Orchid Society Our aim is to promote interest in the study of Native European Orchids and those from similar temperate climates throughout the world. We cover such varied aspects as field study, cultivation and propagation, photography, taxonomy and systematics, and practical conservation. We welcome articles relating to any of these subjects, which will be considered for publication by the editorial committee. Please send your submissions to the Editor, and please structure your text according to the “Advice to Authors” (see website www.hardyorchidsociety.org.uk , January 2004 Journal, Members’ Handbook or contact the Editor). Views expressed in journal arti - cles are those of their author(s) and may not reflect those of HOS. The Hardy Orchid Society Committee President: Prof. Richard Bateman, Jodrell Laboratory, Royal Botanic Gardens Kew, Richmond, Surrey, TW9 3DS Chairman: Celia Wright, The Windmill, Vennington, Westbury, Shrewsbury, Shropshire, SY5 9RG [email protected] Vice-Chairman: vacant Secretary: Richard Robinson, Rhiw, Church Street, Amberley, Sussex, BN18 9NF [email protected] Treasurer: John Wallington, 17, Springbank, Eversley Park Road, London, N21 1JH [email protected] Membership Secretary: Moira Tarrant, Bumbys, Fox Road, Mashbury, Chelmsford, CM1 4TJ [email protected] Plant Show Secretary: David Hughes, Linmoor Cottage, Highwood, -
Regional Vegetation Change and Implications for Local Conservation: an Example from West Cornwall (United Kingdom)
Global Ecology and Conservation 4 (2015) 405–413 Contents lists available at ScienceDirect Global Ecology and Conservation journal homepage: www.elsevier.com/locate/gecco Original research article Regional vegetation change and implications for local conservation: An example from West Cornwall (United Kingdom) A. Kosanic a,∗, K. Anderson b, C.H. Frère c, S. Harrison a a College of Life and Environmental Sciences, University of Exeter, Penryn Campus Penryn TR10 9EZ, United Kingdom b College of Life and Environmental Sciences, ESI, University of Exeter, Penryn Campus Penryn TR10 9EZ, United Kingdom c GeneCology Research Centre, University of Sunshine Coast, 90 Sippy Downs Drive, Sippy Downs QLD 4556, Australia article info a b s t r a c t Article history: This study tracks local vegetation change in West Cornwall (South West England) within Received 2 April 2015 regional context, using historic herbarium (pre-1900) and recent vegetation records (post- Received in revised form 26 August 2015 1900). The focus centres on species lost from the region over the past century. For this study Accepted 26 August 2015 we used a collection of herbarium records published in 1909 (Davey's ``Flora of Cornwall'') Available online 9 September 2015 and contemporary records from the ``New Atlas of British and Irish Flora'' downloaded from the National Biodiversity Network (NBN), online database. Both data sets were spatially Keywords: analysed using ArcGIS in order to detect local scale species loss. Our results showed that Vegetation change Herbarium records species loss was highest in the south (11 plant species), compared to the loss from middle Regional identity areas (6 plant species) and in the northern area (8 plant species) of West Cornwall. -
Botolph's Bridge, Hythe Redoubt, Hythe Ranges West And
Folkestone and Hythe Birds Tetrad Guide: TR13 G (Botolph’s Bridge, Hythe Redoubt, Hythe Ranges West, and Nickolls Quarry) The tetrad TR13 G contains a number of major local hotspots, with Nickolls Quarry, the Botolph’s Bridge area and part of Hythe Ranges located within its boundaries. As a consequence the tetrad has the richest diversity of breeding birds in the local area, with 71 species having a status of at least possible in the latest BTO Atlas survey. It also had the highest total of species (125) in the winter Atlas survey. Sadly a major housing development is now in progress at the Nickolls Quarry site and much of the best habitat is now being disturbed or lost. Nickolls Quarry has been watched since the late 1940s, though early coverage was patchy, particularly in the 1960s and 1970s. As a working quarry the site has undergone significant changes during this time, expanding from two small pits to a much larger area of open water, some of which has since been backfilled. During 2001 to 2004 a series of shallow pools were created which proved particularly attractive to waders. Nickolls Quarry in 1952 Nickolls Quarry in 1998 Looking roughly northwards across the 'old pit' Looking south-west across the site towards the Hythe Roughs towards Dungeness Although a major housing development is underway on the site it still contains some interesting habitats. The lake is easily the largest area of open water in the local area and so remains one of the best areas for wildfowl, particularly during cold weather, for example in December 2010 when there were peak counts of 170 Wigeon, 107 Coot, 104 Pochard, 100 Teal, 53 Tufted Duck, 34 Gadwall, 18 Mute Swan, 12 Pintail, 10 Bewick’s Swan, 8 Shoveler, singles of Goldeneye and Goosander, and 300 White-fronted Geese flew over. -
See Full Species List
County Wildlife Action Name of Site: Billingford Common Surveyors: Lusie Ambler Ann Foreman Nick Lingwood Vicky Rusby Ian Tart Becky Whatley Dates of Surveys 09/04/17, 06/05/17, 19/05/17, 11/06/17, 23/07/17, 12/08/17, 09/09/17 Plus additional casual visits Scientific Name Common Name Comp 1 Comp 2 Comp 3 Comp 4 Comp 5 DAFOR Comment/Location Achillea millefolium Yarrow 1 2 4 O Aegopodium podagraria Ground Elder 3 4 O Agrimonia eupatoria Agrimony 1 R Agrostis canina Velvet Bent 5 R Agrostis capillaris Common Bent 1 5 F Agrostis gigantea Black Bent 5 R Alliaria petiolata Garlic Mustard 2 5 O Alnus glutinosa Alder 3 R Alopecurus myosuroides Black-grass 1 R Alopecurus pratensis Meadow Foxtail 1 2 LA Angelica sylvestris Wild Angelica 1 2 3 4 O Anisantha sterilis Barren Brome 1 4 LF Anthriscus sylvestris Cowparsley 1 2 LF Aphanes agg Parsley Piert agg 1 R Apium nodiflorum Fool's Watercress 2 R In ditch Arabidopsis thaliana Thale Cress 2 R Arctium lappa Greater Burdock 2 O Arctium minus Lesser Burdock 1 4 O Arenaria serpyllifolia Thyme-leaved sandwort 1 R Aria praecox Early Hair-grass 1 R Armoracia rusticana Horseradish 1 O Large patches Arrhenatherum elatius False Oat-grass 1 2 LD/LA Artemisia vulgaris Mugwort 1 2 4 LF Arum maculatum Lords and Ladies 3 5 R Ballota nigra Black Horehound 1 4 R Barberea sp Cress sp 2 R In ditch Bellis perennis Daisy 2 R Berula erecta Lesser Water Parsnip 4 R Riverside Betula pendula Silver Birch 1 R Saplings Bromus sterilis Barren Brome 1 R Calystegia sepium Hedge Bindweed 2 4 O Capsella bursa-pastoris Shepherd's -
Federico Selvi a Critical Checklist of the Vascular Flora of Tuscan Maremma
Federico Selvi A critical checklist of the vascular flora of Tuscan Maremma (Grosseto province, Italy) Abstract Selvi, F.: A critical checklist of the vascular flora of Tuscan Maremma (Grosseto province, Italy). — Fl. Medit. 20: 47-139. 2010. — ISSN 1120-4052. The Tuscan Maremma is a historical region of central western Italy of remarkable ecological and landscape value, with a surface of about 4.420 km2 largely corresponding to the province of Grosseto. A critical inventory of the native and naturalized vascular plant species growing in this territory is here presented, based on over twenty years of author's collections and study of relevant herbarium materials and literature. The checklist includes 2.056 species and subspecies (excluding orchid hybrids), of which, however, 49 should be excluded, 67 need confirmation and 15 have most probably desappeared during the last century. Considering the 1.925 con- firmed taxa only, this area is home of about 25% of the Italian flora though representing only 1.5% of the national surface. The main phytogeographical features in terms of life-form distri- bution, chorological types, endemic species and taxa of particular conservation relevance are presented. Species not previously recorded from Tuscany are: Anthoxanthum ovatum Lag., Cardamine amporitana Sennen & Pau, Hieracium glaucinum Jord., H. maranzae (Murr & Zahn) Prain (H. neoplatyphyllum Gottschl.), H. murorum subsp. tenuiflorum (A.-T.) Schinz & R. Keller, H. vasconicum Martrin-Donos, Onobrychis arenaria (Kit.) DC., Typha domingensis (Pers.) Steud., Vicia loiseleurii (M. Bieb) Litv. and the exotic Oenothera speciosa Nutt. Key words: Flora, Phytogeography, Taxonomy, Tuscan Maremma. Introduction Inhabited by man since millennia and cradle of the Etruscan civilization, Maremma is a historical region of central-western Italy that stretches, in its broadest sense, from south- ern Tuscany to northern Latium in the provinces of Pisa, Livorno, Grosseto and Viterbo. -
Diversity of the Moth Fauna (Lepidoptera: Heterocera) of a Wetland Forest: a Case Study from Motovun Forest, Istria, Croatia
PERIODICUM BIOLOGORUM UDC 57:61 VOL. 117, No 3, 399–414, 2015 CODEN PDBIAD DOI: 10.18054/pb.2015.117.3.2945 ISSN 0031-5362 original research article Diversity of the moth fauna (Lepidoptera: Heterocera) of a wetland forest: A case study from Motovun forest, Istria, Croatia Abstract TONI KOREN1 KAJA VUKOTIĆ2 Background and Purpose: The Motovun forest located in the Mirna MITJA ČRNE3 river valley, central Istria, Croatia is one of the last lowland floodplain 1 Croatian Herpetological Society – Hyla, forests remaining in the Mediterranean area. Lipovac I. n. 7, 10000 Zagreb Materials and Methods: Between 2011 and 2014 lepidopterological 2 Biodiva – Conservation Biologist Society, research was carried out on 14 sampling sites in the area of Motovun forest. Kettejeva 1, 6000 Koper, Slovenia The moth fauna was surveyed using standard light traps tents. 3 Biodiva – Conservation Biologist Society, Results and Conclusions: Altogether 403 moth species were recorded Kettejeva 1, 6000 Koper, Slovenia in the area, of which 65 can be considered at least partially hygrophilous. These results list the Motovun forest as one of the best surveyed regions in Correspondence: Toni Koren Croatia in respect of the moth fauna. The current study is the first of its kind [email protected] for the area and an important contribution to the knowledge of moth fauna of the Istria region, and also for Croatia in general. Key words: floodplain forest, wetland moth species INTRODUCTION uring the past 150 years, over 300 papers concerning the moths Dand butterflies of Croatia have been published (e.g. 1, 2, 3, 4, 5, 6, 7, 8). -
Evolution of VRN2/Ghd7-Like Genes in Vernalization-Mediated Repression of Grass Flowering1[OPEN]
Evolution of VRN2/Ghd7-Like Genes in Vernalization-Mediated Repression of Grass Flowering1[OPEN] Daniel P. Woods2,MeghanA.McKeown2, Yinxin Dong, Jill C. Preston, and Richard M. Amasino* Laboratory of Genetics, U.S. Department of Energy Great Lakes Bioenergy Research Center (D.P.W., R.M.A.), and Department of Biochemistry (D.P.W., Y.D., R.M.A.), University of Wisconsin, Madison, Wisconsin 53706; Department of Plant Biology, University of Vermont, Burlington, Vermont 05405 (M.A.M., J.C.P.); and College of Horticulture, Northwest A&F University, Yangling, Shaanxi 712100, People’s Republic of China (Y.D.) ORCID IDs: 0000-0002-1498-5707 (D.P.W.); 0000-0002-0187-4135 (Y.D.); 0000-0002-9211-5061 (J.C.P.); 0000-0003-3068-5402 (R.M.A.). Flowering of many plant species is coordinated with seasonal environmentalcuessuchastemperatureand photoperiod. Vernalization provides competence to flower after prolonged cold exposure, and a vernalization requirement prevents flowering from occurring prior to winter. In winter wheat (Triticum aestivum)andbarley(Hordeum vulgare), three genes VRN1, VRN2,andFT form a regulatory loop that regulates the initiation of flowering. Prior to cold exposure, VRN2 represses FT. During cold, VRN1 expression increases, resulting in the repression of VRN2, which in turn allows activation of FT during long days to induce flowering. Here, we test whether the circuitry of this regulatory loop is conserved across Pooideae, consistent with their niche transition from the tropics to the temperate zone. Our phylogenetic analyses of VRN2-like genes reveal a duplication event occurred before the diversification of the grasses that gave rise to a CO9 and VRN2/Ghd7 clade and support orthology between wheat/barley VRN2 and rice (Oryza sativa) Ghd7.OurBrachypodium distachyon VRN1 and VRN2 knockdown and overexpression experiments demonstrate functional conservation of grass VRN1 and VRN2 in the promotion and repression of flowering, respectively. -
8. Tribe BRYLKINIEAE 54. BRYLKINIA F. Schmidt, Mém. Acad. Imp
212 POACEAE ma 9–10 mm, loosely pubescent in lower 1/4–1/2; awn 1.3–1.7 Sichuan, Xizang, Yunnan [Bhutan, N India, Kashmir, N Myan- cm, stiffly hispid at base, hairs 0.5–0.8 mm, scabrid above. mar, Nepal]. Anthers 2–3 mm. Fl. and fr. Aug–Oct. The long, retrorse spines at the lemma apex are an unmistakable Open grassy mountainsides, forest clearings; 2700 m and above. distinguishing feature of this species. 8. Tribe BRYLKINIEAE 扁穗草族 bian sui cao zu Wu Zhenlan (吴珍兰); Sylvia M. Phillips Perennial. Leaf sheaths with connate margins; leaf blades linear, transverse veinlets present; ligule very short, membranous. Inflorescence a lax raceme. Spikelets with 1 fertile floret, 2 sterile empty lemmas below and a rachilla extension above, strongly laterally compressed, falling entire together with the pedicel; glumes unequal, narrowly lanceolate, shorter than lemmas, herbaceous, 3–5-veined, apex acuminate to caudate; lemmas lanceolate, thinly leathery, strongly keeled, 5–7-veined, sterile lemmas acuminate to short-awned, fertile lemma with a straight awn from apex; palea keels closely adjacent. Lodicules 2, free, fairly large, rectangular, hyaline. Stamens 3. Caryopsis narrowly ellipsoid, apex with glossy rounded caplike appendage with central knob from style base, embryo small, hilum linear, slightly shorter than caryopsis. Leaf anatomy: non-Kranz; microhairs absent. x = 10. One species: China, Japan, E Russia. This is a unispecific tribe of uncertain affinity, found in cool, temperate forests. 54. BRYLKINIA F. Schmidt, Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7, 12: 199. 1868. 扁穗草属 bian sui cao shu Description and distribution as for tribe.