Plant Identification Key for the Results-Based Environment-Agri Pilot Programme
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Lathyrus Bijugatus
Fire Effects Information System (FEIS) FEIS Home Page Lathyrus bijugatus Table of Contents SUMMARY INTRODUCTION DISTRIBUTION AND OCCURRENCE BOTANICAL AND ECOLOGICAL CHARACTERISTICS FIRE ECOLOGY AND MANAGEMENT OTHER MANAGEMENT CONSIDERATIONS APPENDIX REFERENCES Figure 1—Drypark pea in flower. Photo by Tara Luna, used with permission. SUMMARY This Species Review summarizes the scientific information that was available on drypark pea as of February 2021. Drypark pea is a rare, leguminous forb that occurs in eastern Washington and Oregon, northern Idaho, and northwestern Montana. Within that distribution, it grows in a broad range of biogeoclimatic zones and elevations. As its common name "drypark pea" suggests, it prefers dry soils and open sites. Drypark pea grows in sagebrush-conifer and sagebrush-grassland transition zones; in ponderosa pine, Douglas-fir, and subalpine fir-Engelmann spruce woodlands and forests; and subalpine fir parklands. In conifer communities, it is most common in open stands. Drypark pea has rhizomes that grow out from its taproot. Its roots host nitrogen-fixing Rhizobium bacteria. Drypark pea regenerates from seed and has a soil-stored seed bank; however, information on seed dispersal, viability, and seedling establishment of drypark pea was not available in the literature. Fire probably top-kills drypark pea, and it likely sprouts from its rhizomes and/or caudex after top-kill; however, these responses are undocumented. Only one study provided information on the response of drypark pea to fire. In ponderosa pine forest in northern Idaho, cover and frequency of drypark pea were similar on unburned plots and plots burned under low or high intensity, when 1 averaged across 3 postfire years. -
Leptidea Reali (Real’S Wood White) in Northern Ireland
The ecology and conservation of Leptidea reali (Real’s Wood White) in Northern Ireland © Neal Warnock Neal Warnock September 2008 11753072 MSc Ecological Management and Conservation Biology, Queen’s University Belfast TABLE OF CONTENTS CONTENTS PAGE NUMBER Acknowledgements…………………………………………………………………….…....i Abstract……………………………………………………………………………………...ii List of tables………………………………………………………………………………...iii List of figures……………………………………………………………………………..... iv 1 Introduction……………………………………………………………….1 1.1 Background……………………………………………………………………...1 1.2 ‘Wood White’ butterflies……………………… ……………………………...2 1.2.1 The ‘sinapis-reali’ complex………………………………………....2 1.2.2 Leptidea reali in Northern Ireland- what we know and what we Don’t know………………………………………………………………….9 1.3 Summary and Aims of study…………………………………………………...12 2 Sites and Methods……………………………………………………….15 2.1 Site locations…………………………………………………………………..15 2.2 Relationships with previous research……………………………………….…16 2.3 Site descriptions............................................................................................…..18 2.3.1 Craigavon Lakes…………………………………………………………18 2.3.2 Oxford Island National Nature Reserve……………………………….....20 2.4 Numbers………………………………………………………………………..23 2.5 Oviposition choice- flight cage experiment……………………………...…….24 2.6 Oviposition preference- field observations…………………………………….24 2.7 Larvae and pupae………………………………………………………………25 2.8 Nectaring preference…………………………………………………..……….25 2.9 Courtship……………………………………………………………………….25 2.10 Species identification…………………………………………………………26 2.11 -
Effect of Broad Bean Varieties and Faba Bean Upon Populations Dynamic of Bruchus Rufimanus (Coleoptera: Chrysomelidae: Bruchinae) in Kabylia Region (Algeria)
International Journal of Agricultural Science and Research (IJASR) ISSN(P): 2250-0057; ISSN(E): 2321-0087 Vol. 5, Issue 6, Dec 2015, 79-88 © TJPRC Pvt. Ltd. EFFECT OF BROAD BEAN VARIETIES AND FABA BEAN UPON POPULATIONS DYNAMIC OF BRUCHUS RUFIMANUS (COLEOPTERA: CHRYSOMELIDAE: BRUCHINAE) IN KABYLIA REGION (ALGERIA) MEZANI SAMIR, KHELFANE-GOUCEM KARIMA & MEDJDOUB-BENSAAD FERROUDJA Biology Department, Mouloud Mammeri University, Tizi-Ouzou, Algeria ABSTRACT The present study aimed to examine the process and conditions of broad bean Bruchid B. rufimanus infestation in the field in Kabylia region (Algeria). B. rufimanus adults colonized progressively the cultures of Aguadulce variety and faba bean at the beginning of the flowering period, while it colonized Seville variety culture during the flowering period. This colonization seemed to depend upon climatic factors and host plant phenology. The presence of adults in plots spanned about 5 weeks for Aguadulce variety, 6 for faba bean and 4 weeks for Seville variety. At the end of the flowering period, the number of adults decreased whereas the number of mature pods increased for all plots. The egg-laying was spread over a period of approximately 8 and 7 weeks for Aguadulce and Seville varieties respectively and 6 for faba bean. Females seemed Article Original to deposit their eggs randomly on the available young pods and old pods of each host. Our results showed also that the varieties act significantly on the rate of infestation by B. rufimanus females on V. faba plots studied. KEYWORDS: Vicia Faba, Bruchus Rufimanus, Egg-Laying, Varieties, Host Plant Colonization, Kabylia Region Received: Oct 06, 2015; Accepted: Oct 19, 2015; Published: Oct 27, 2015; Paper Id.: IJASRDEC201511 INTRODUCTION Bean or faba bean ( Vicia faba Linné) is a most cultivated Leguminosae seeds for human consumption in the Maghreb (Kharrat and al., 2002). -
Atlas of the Flora of New England: Fabaceae
Angelo, R. and D.E. Boufford. 2013. Atlas of the flora of New England: Fabaceae. Phytoneuron 2013-2: 1–15 + map pages 1– 21. Published 9 January 2013. ISSN 2153 733X ATLAS OF THE FLORA OF NEW ENGLAND: FABACEAE RAY ANGELO1 and DAVID E. BOUFFORD2 Harvard University Herbaria 22 Divinity Avenue Cambridge, Massachusetts 02138-2020 [email protected] [email protected] ABSTRACT Dot maps are provided to depict the distribution at the county level of the taxa of Magnoliophyta: Fabaceae growing outside of cultivation in the six New England states of the northeastern United States. The maps treat 172 taxa (species, subspecies, varieties, and hybrids, but not forms) based primarily on specimens in the major herbaria of Maine, New Hampshire, Vermont, Massachusetts, Rhode Island, and Connecticut, with most data derived from the holdings of the New England Botanical Club Herbarium (NEBC). Brief synonymy (to account for names used in standard manuals and floras for the area and on herbarium specimens), habitat, chromosome information, and common names are also provided. KEY WORDS: flora, New England, atlas, distribution, Fabaceae This article is the eleventh in a series (Angelo & Boufford 1996, 1998, 2000, 2007, 2010, 2011a, 2011b, 2012a, 2012b, 2012c) that presents the distributions of the vascular flora of New England in the form of dot distribution maps at the county level (Figure 1). Seven more articles are planned. The atlas is posted on the internet at http://neatlas.org, where it will be updated as new information becomes available. This project encompasses all vascular plants (lycophytes, pteridophytes and spermatophytes) at the rank of species, subspecies, and variety growing independent of cultivation in the six New England states. -
Towards Resolving Lamiales Relationships
Schäferhoff et al. BMC Evolutionary Biology 2010, 10:352 http://www.biomedcentral.com/1471-2148/10/352 RESEARCH ARTICLE Open Access Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences Bastian Schäferhoff1*, Andreas Fleischmann2, Eberhard Fischer3, Dirk C Albach4, Thomas Borsch5, Günther Heubl2, Kai F Müller1 Abstract Background: In the large angiosperm order Lamiales, a diverse array of highly specialized life strategies such as carnivory, parasitism, epiphytism, and desiccation tolerance occur, and some lineages possess drastically accelerated DNA substitutional rates or miniaturized genomes. However, understanding the evolution of these phenomena in the order, and clarifying borders of and relationships among lamialean families, has been hindered by largely unresolved trees in the past. Results: Our analysis of the rapidly evolving trnK/matK, trnL-F and rps16 chloroplast regions enabled us to infer more precise phylogenetic hypotheses for the Lamiales. Relationships among the nine first-branching families in the Lamiales tree are now resolved with very strong support. Subsequent to Plocospermataceae, a clade consisting of Carlemanniaceae plus Oleaceae branches, followed by Tetrachondraceae and a newly inferred clade composed of Gesneriaceae plus Calceolariaceae, which is also supported by morphological characters. Plantaginaceae (incl. Gratioleae) and Scrophulariaceae are well separated in the backbone grade; Lamiaceae and Verbenaceae appear in distant clades, while the recently described Linderniaceae are confirmed to be monophyletic and in an isolated position. Conclusions: Confidence about deep nodes of the Lamiales tree is an important step towards understanding the evolutionary diversification of a major clade of flowering plants. The degree of resolution obtained here now provides a first opportunity to discuss the evolution of morphological and biochemical traits in Lamiales. -
PLANT LIST for POLLINATORS Part 1 – a Concise List of Suggested Garden Plants That Are Attractive to Pollinating Insects
THE ACTION PLAN FOR POLLINATORS SUGGESTED PLANT LIST FOR POLLINATORS Part 1 – A concise list of suggested garden plants that are attractive to pollinating insects This is a list of suggested garden plants. We have only selected flowers which are garden- worthy, easily obtainable, well-known, and widely acknowledged as being attractive to pollinating insects. In some case we have given extra comments about garden- worthiness. This is intended as a clear and concise short list to help gardeners; it is not intended to be comprehensive and we have avoided suggesting plants which are difficult to grow or obtain, or whose benefit to pollinators is still a matter for debate. We have omitted several plants that are considered to have invasive potential, and have qualified some others on the list with comments advising readers how to avoid invasive forms. PLANT ANGELICA (Angelica species). Attractive to a range of insects, especially hoverflies and solitary bees. AUBRETIA (Aubrieta deltoides hybrids). An important early nectar for insects coming out of hibernation. BELLFLOWER (Campanula species and cultivars). Forage for bumblebees and some solitary bees. BETONY (Stachys officinalis). Attractive to bumblebees. Butterfly Conversation’s Awarded the Royal Horticultural Top Butterflys Society’s ‘Award of Garden Nectar Plants. Merit’. PLANT BIRD’S FOOT TREFOIL (Lotus corniculatus). Larval food plant for Common Blue, Dingy Skipper and several moths. Also an important pollen source for bumblebees. Can be grown in gravel or planted in a lawn that is mowed with blades set high during the flowering period. BOWLES’ WALLFLOWER (Erysimum Bowles Mauve). Mauve perennial wallflower, long season nectar for butterflies, moths and many bee species. -
Pollination and Evolution in Pedicularis (Scrophulariaceae) Elizabeth F
Aliso: A Journal of Systematic and Evolutionary Botany Volume 5 | Issue 2 Article 6 1962 Pollination and Evolution in Pedicularis (Scrophulariaceae) Elizabeth F. Sprague Sweet Briar College Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Sprague, Elizabeth F. (1962) "Pollination and Evolution in Pedicularis (Scrophulariaceae)," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 5: Iss. 2, Article 6. Available at: http://scholarship.claremont.edu/aliso/vol5/iss2/6 ALISO VoL. 5, No.2, pp. 181-209 MARCH 30, 1962 POLLINATION AND EVOLUTION IN PEDICULARIS (SCROPHULARIACEAE) 1 ELIZABETH F. SPRAGUE Sweet Briar College, Sweet Briar, Virginia Pedicularis is a circumboreal and North Temperate genus of semi-parasitic herbs belong ing to the tribe Euphrasieae. The complex flower shape is typical of bee flowers. The mode of pollination for seven species occurring in California has been studied. The purpose of this paper is to present data on pollination mechanisms of some western North American species and to relate these findings to the evolution of the genus. The seven species observed all fall into Li's (1948) infrageneric group, Allopbyllum, of alternate-leaved species with alternate flowers and terminal spicate or racemose inflores cences. They represent six of the eleven coastal series recognized by Pennell ( 1951) as natural groups having very homogeneous vegetative and floral characters. The following species were observed in California: P. crenulata occurs in the Rocky Mountains in Colorado, Wyoming, west into Nevada, and in a tiny relictual outpost of 25-30 white-flowering plants on Convict Creek, Inyo County, California. -
Incidence of Polyploidy and Genome Evolution in Scrophulariaceae S.L
DEPARTAMENTO DE CIÊNCIAS DA VIDA FACULDADE DE CIÊNCIAS E TECNOLOGIA UNIVERSIDADE DE COIMBRA Incidence of polyploidy and genome evolution in Scrophulariaceae s.l. Digitalis mariana subsp. heywoodii Mariana Oliveira e Castro 2011 DEPARTAMENTO DE CIÊNCIAS DA VIDA FACULDADE DE CIÊNCIAS E TECNOLOGIA UNIVERSIDADE DE COIMBRA Incidence of polyploidy and genome evolution in Scrophulariaceae s.l. Dissertação apresentada à Universidade de Coimbra para cumprimento dos requisitos necessários à obtenção do grau de Mestre em 2011, realizada sob a orientação científica do Professor Doutor João Carlos Mano Castro Loureiro (Universidade de Coimbra) e da Doutora Sílvia Raquel Cardoso Castro Loureiro (Universidade de Coimbra) Mariana Oliveira e Castro 2011 Acknowledgements First, I want to thank to all the people who always supported me and directly or indirectly contributed for the accomplishment of the present work. I am grateful to João Loureiro and Sílvia Castro for accepting the supervision of this work, for all their support and friendship and for the continuous encourage for making science. I also thank to Dr Jorge Paiva for taxonomic lessons and for all his support in the corrent identification of some plant material. I want to thank to the Index Semina of COI, UPT, ISAUTL and MHNM for sending Scrophulariaceae seeds. I want to thank to Prof. Conceição Santos and Helena Oliveira for enabling the use of the flow cytometer of the Laboratory of Biotechnology and Cytomics (Department of Biology, University of Aveiro) in the first stages of this thesis. I do not forget all the members (official or borrowed) of the Plant Ecology and Evolution Group for their friendship and for the excellent work environment. -
Appendix: Patierns of Specialization
APPENDIX: PATIERNS OF SPECIALIZATION Statistical rationale progress, a second variant of cluster analysis may be considered more appropriate here. In optimal (non-hierarchical) clustering, A variety of ways is available for exploring axes or groupings the analysis sorts the species into a variable number of internally within multivariate data sets. Principal components analysis, for homogeneous clusters. Group properties of the cluster then example, would identify any axes of specialization to which the become equally important as properties of their individual different attributes might variously contribute, both in kind and in members, and the analysis will not necessarily produce the same degree. However, the most suitable indication arises from the outcome as would an hierarchical analysis into the same number assumption that the values of certain attributes for a particular of clusters. group of species have evolved through simultaneous selection-a This is the approach which we, and Grime eta/. (1987), have composite response on the part of several attributes to a set of followed. They are both successive instances of a 'rolling external environmental pressures. Further, these sets of attributes synthesis', a research strategy which periodically draws together may well have evolved in such a way that coherent groupings of the current state of quantitative knowledge of native plant species species which possess them can now be identified, each with into a statistical and comparative overview. characteristic values, or ranges of values, for each of the attributes. This being so, a cluster analysis is indicated. Two variants of cluster analysis exist. The first employs a The current database hierarchical method in which each species belongs initially to its own separate class. -
The Linderniaceae and Gratiolaceae Are Further Lineages Distinct from the Scrophulariaceae (Lamiales)
Research Paper 1 The Linderniaceae and Gratiolaceae are further Lineages Distinct from the Scrophulariaceae (Lamiales) R. Rahmanzadeh1, K. Müller2, E. Fischer3, D. Bartels1, and T. Borsch2 1 Institut für Molekulare Physiologie und Biotechnologie der Pflanzen, Universität Bonn, Kirschallee 1, 53115 Bonn, Germany 2 Nees-Institut für Biodiversität der Pflanzen, Universität Bonn, Meckenheimer Allee 170, 53115 Bonn, Germany 3 Institut für Integrierte Naturwissenschaften ± Biologie, Universität Koblenz-Landau, Universitätsstraûe 1, 56070 Koblenz, Germany Received: July 14, 2004; Accepted: September 22, 2004 Abstract: The Lamiales are one of the largest orders of angio- Traditionally, Craterostigma, Lindernia and their relatives have sperms, with about 22000 species. The Scrophulariaceae, as been treated as members of the family Scrophulariaceae in the one of their most important families, has recently been shown order Lamiales (e.g., Takhtajan,1997). Although it is well estab- to be polyphyletic. As a consequence, this family was re-classi- lished that the Plocospermataceae and Oleaceae are their first fied and several groups of former scrophulariaceous genera branching families (Bremer et al., 2002; Hilu et al., 2003; Soltis now belong to different families, such as the Calceolariaceae, et al., 2000), little is known about the evolutionary diversifica- Plantaginaceae, or Phrymaceae. In the present study, relation- tion of most of the orders diversity. The Lamiales branching ships of the genera Craterostigma, Lindernia and its allies, hith- above the Plocospermataceae and Oleaceae are called ªcore erto classified within the Scrophulariaceae, were analyzed. Se- Lamialesº in the following text. The most recent classification quences of the chloroplast trnK intron and the matK gene by the Angiosperm Phylogeny Group (APG2, 2003) recognizes (~ 2.5 kb) were generated for representatives of all major line- 20 families. -
SPECIES IDENTIFICATION GUIDE National Plant Monitoring Scheme SPECIES IDENTIFICATION GUIDE
National Plant Monitoring Scheme SPECIES IDENTIFICATION GUIDE National Plant Monitoring Scheme SPECIES IDENTIFICATION GUIDE Contents White / Cream ................................ 2 Grasses ...................................... 130 Yellow ..........................................33 Rushes ....................................... 138 Red .............................................63 Sedges ....................................... 140 Pink ............................................66 Shrubs / Trees .............................. 148 Blue / Purple .................................83 Wood-rushes ................................ 154 Green / Brown ............................. 106 Indexes Aquatics ..................................... 118 Common name ............................. 155 Clubmosses ................................. 124 Scientific name ............................. 160 Ferns / Horsetails .......................... 125 Appendix .................................... 165 Key Traffic light system WF symbol R A G Species with the symbol G are For those recording at the generally easier to identify; Wildflower Level only. species with the symbol A may be harder to identify and additional information is provided, particularly on illustrations, to support you. Those with the symbol R may be confused with other species. In this instance distinguishing features are provided. Introduction This guide has been produced to help you identify the plants we would like you to record for the National Plant Monitoring Scheme. There is an index at -
WLGF Pollinator Planting List
Suggested Plant List for Pollinators, September 2014 This list has been produced by Jan Miller on behalf of the North Wales Wildlife Trust and Marc Carlton on behalf of the Wildlife Gardening Forum, at the request of the Welsh Government’s Pollinator Task Force. The authors recognise that producing planting lists for pollinators is not a straightforward exercise. There are still many areas where further research is required in order to improve our understanding of the needs of pollinating insects and the best planting schemes to cater for them. One of the Wildlife Gardening Forum’s aims is to promote more evidence-based research to increase our knowledge and understanding of this subject. This list is based on the compilers’ personal experience over many years as gardeners and naturalists, and incorporates Jan’s work investigating plants for butterflies on behalf of Butterfly Conservation and uses their data sent in by members over twenty years. The list includes a selection of forage plants useful for adult butterflies, moths, hoverflies, bumblebees and solitary bees, which together make up the vast majority of pollinators in Wales. Plants recommended as larval food plants for butterflies and some moths have also been included. Specialised lists of flowers that are recommended as forage for honeybees have been published for many years within the beekeeping community and so we have not specifically covered honeybees in our list, although many of the flowers on our list will be used by honeybees. The list is in two parts. The first part is a list of suggested garden plants. We have only selected flowers which are garden-worthy, easily obtainable, well-known, and widely acknowledged as being attractive to pollinating insects.