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Processing Tomato Enterprise Management Plan Tomato Potato Psyllid Processing Tomato Enterprise Management Plan
Processing tomato Enterprise management plan Tomato potato psyllid Processing tomato enterprise management plan CONTENTS INTRODUCTION 1 UNDERSTANDING PEST AND PATHOGEN BIOLOGY AND THEIR IDENTIFICATION 2 IDENTIFYING RISK PATHWAYS 5 APPLYING CONTROL AND MANAGEMENT OPTIONS 6 BIOSECURITY AWARENESS AND IMPLEMENTATION 12 MOVEMENT OF FRUIT TO PROCESSING FACILITY 13 PERMIT 14 APPENDIX 1 — Preliminary results 15 APPENDIX 2 — Biological control results 19 APPENDIX 3 — Chemical control results 23 MY NOTES 27 Tomato potato psyllid Processing tomato enterprise management plan 1 INTRODUCTION Tomato potato psyllid (TPP) is supporting ongoing efforts to renew and a serious pest of Processing maintain market access, as well as underpin tomatoes. TPP is the vector certification and assurance schemes. of the bacterium Candidatus Our aim is to build on current best practice Liberibacter solanacearum* to include the management of TPP, without (CLso) which is associated with creating unnecessary additional work. a range of symptoms that affect the production and economic THIS PLAN INCLUDES FIVE KEY performance of your crop. COMPONENTS: TPP WAS FIRST DETECTED TPP was first detected on mainland Australia UNDERSTANDING PEST AND in Western Australia (WA) in February 2017. ON MAINLAND AUSTRALIA PATHOGEN BIOLOGY AND THEIR This prompted a comprehensive biosecurity IN WESTERN AUSTRALIA IN response to minimise the impact of TPP on IDENTIFICATION FEBRUARY 2017. Australian businesses. After national agreement TPP could not be IDENTIFYING RISK PATHWAYS * As at October 2018, surveillance eradicated, efforts focussed on developing the confirms that CLso is not present science, biosecurity and business systems to in WA improve the capacity of growers and industry to manage TPP. APPLYING CONTROL AND An essential component of transition to MANAGEMENT OPTIONS management is the development and implementation of enterprise management plans for affected industries. -
Appendix 1: Maps and Plans Appendix184 Map 1: Conservation Categories for the Nominated Property
Appendix 1: Maps and Plans Appendix184 Map 1: Conservation Categories for the Nominated Property. Los Alerces National Park, Argentina 185 Map 2: Andean-North Patagonian Biosphere Reserve: Context for the Nominated Proprty. Los Alerces National Park, Argentina 186 Map 3: Vegetation of the Valdivian Ecoregion 187 Map 4: Vegetation Communities in Los Alerces National Park 188 Map 5: Strict Nature and Wildlife Reserve 189 Map 6: Usage Zoning, Los Alerces National Park 190 Map 7: Human Settlements and Infrastructure 191 Appendix 2: Species Lists Ap9n192 Appendix 2.1 List of Plant Species Recorded at PNLA 193 Appendix 2.2: List of Animal Species: Mammals 212 Appendix 2.3: List of Animal Species: Birds 214 Appendix 2.4: List of Animal Species: Reptiles 219 Appendix 2.5: List of Animal Species: Amphibians 220 Appendix 2.6: List of Animal Species: Fish 221 Appendix 2.7: List of Animal Species and Threat Status 222 Appendix 3: Law No. 19,292 Append228 Appendix 4: PNLA Management Plan Approval and Contents Appendi242 Appendix 5: Participative Process for Writing the Nomination Form Appendi252 Synthesis 252 Management Plan UpdateWorkshop 253 Annex A: Interview Guide 256 Annex B: Meetings and Interviews Held 257 Annex C: Self-Administered Survey 261 Annex D: ExternalWorkshop Participants 262 Annex E: Promotional Leaflet 264 Annex F: Interview Results Summary 267 Annex G: Survey Results Summary 272 Annex H: Esquel Declaration of Interest 274 Annex I: Trevelin Declaration of Interest 276 Annex J: Chubut Tourism Secretariat Declaration of Interest 278 -
The First New Zealand Insects Collected on Cook's
Pacific Science (1989), vol.43, 43, nono.. 1 © 1989 by UniversityUniversity of Hawaii Press.Pres s. All rights reserved TheThe First New Zealand Zealand InsectsInsects CollectedCollectedon Cook'sCook's Endeavour Voyage!Voyage! 2 J. R. H. AANDREWSNDREWS2 AND G.G . W. GIBBSGmBS ABSTRACT:ABSTRACT: The Banks collection of 40 insect species, species, described by J. J. C.C. Fabricius in 1775,1775, is critically examined to explore the possible methods of collection and to document changesto the inseinsectct fauna andto the original collection localities sincsincee 1769.The1769. The aassemblagessemblageof species is is regarded as unusual. unusual. It includes insects that are large large and colorful as well as those that are small and cryptic;cryptic; some species that were probably common were overlooked, but others that are today rare were taken.taken. It is concluded that the Cook naturalists caught about 15species with a butterfly net, but that the majority (all CoColeoptera)leoptera) were discoveredin conjunction with other biobiologicallogical specimens, especially plantsplants.. PossibPossiblele reasons for the omission ofwetwetasas,, stick insects, insects, etc.,etc., are discussed. discussed. This early collection shows that marked changesin abundance may have occurred in some speciespeciess since European colonizationcolonization.. One newrecord is is revealed:revealed: The cicada NotopsaltaNotopsaltasericea sericea (Walker) was found to be among the Fabricius specispeci mens from New Zealand,Zealand, but itsits description evidentlyevidently -
Focus on High Country and Auckland North | Lizard Habitat | Native Vines
Open space $7.50 MAGAZINE OF THE QUEEN ELIZABETH II NATIONAL TRUST ISSUE 75 | MARCH 2009 Focus on High Country and Auckland North | Lizard Habitat | Native Vines Regional Representatives Contents Far North Greg Blunden Ph 09 407 1119 [email protected] 3 News and Events Kaipara Nick Matich 9 Ph 09 439 8932 [email protected] 4 Focus: High Country Whangarei Nan Pullman 7 Focus: Auckland North Ph/Fax 09 434 3457 [email protected] Northwest Auckland Dan Godoy 11 Research: Lizard diversity and abundance Ph 09 529 2474 [email protected] South Auckland Lynda Fleming 12 Protecting the habitat of skinks and geckos Ph 09 238 5739 [email protected] 15 Research: Forest remnant resilience Coromandel – Hauraki Hamish Kendal Ph 07 866 0770 [email protected] 12 16 Waikato tawa forest covenants Waikato Rex Webby Ph 07 853 2504 [email protected] 17 Fencing: Historic Southland fence East Waikato Hamish Dean 18 Know your natives: Vines Ph 021 741 222 [email protected] Waitomo – Otorohanga Malcolm Mackenzie 21 Dairy farms: Protecting bush remnants Ph 07 873 7728 [email protected] Bay of Plenty Hamish Dean 22 Recording ecological changes Ph 021 741 222 [email protected] 25 Fragments 18 Gisborne Malcolm Piper Ph/Fax 06 867 0255 [email protected] 26 Archaeological sites: Hawke’s Bay kumara pits Hawke’s Bay Troy Duncan Ph 06 844 3838 [email protected] 27 Covenants update Taranaki Neil Phillips 29 Trust people Ph 06 753 6433 [email protected] Taupo-Ruapehu Hamish Dean 30 About QEII Trust Ph 021 741 222 [email protected] 32 Rangitikei – Manawatu – Wanganui 32 In the community: Ruahine School Bush John Williamson Ph 06 328 6851 [email protected] Tararua Bill Wallace Helping you protect the special nature of your land Ph 06 376 7796 [email protected] QEII Trust helps landowners to protect significant natural and cultural features on Wairarapa Trevor Thompson their land. -
Gondwanan Origin of Major Monocot Groups Inferred from Dispersal-Vicariance Analysis Kåre Bremer Uppsala University
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 3 2006 Gondwanan Origin of Major Monocot Groups Inferred from Dispersal-Vicariance Analysis Kåre Bremer Uppsala University Thomas Janssen Muséum National d'Histoire Naturelle Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Bremer, Kåre and Janssen, Thomas (2006) "Gondwanan Origin of Major Monocot Groups Inferred from Dispersal-Vicariance Analysis," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 3. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/3 Aliso 22, pp. 22-27 © 2006, Rancho Santa Ana Botanic Garden GONDWANAN ORIGIN OF MAJOR MONO COT GROUPS INFERRED FROM DISPERSAL-VICARIANCE ANALYSIS KARE BREMERl.3 AND THOMAS JANSSEN2 lDepartment of Systematic Botany, Evolutionary Biology Centre, Norbyvagen l8D, SE-752 36 Uppsala, Sweden; 2Museum National d'Histoire Naturelle, Departement de Systematique et Evolution, USM 0602: Taxonomie et collections, 16 rue Buffon, 75005 Paris, France 3Corresponding author ([email protected]) ABSTRACT Historical biogeography of major monocot groups was investigated by biogeographical analysis of a dated phylogeny including 79 of the 81 monocot families using the Angiosperm Phylogeny Group II (APG II) classification. Five major areas were used to describe the family distributions: Eurasia, North America, South America, Africa including Madagascar, and Australasia including New Guinea, New Caledonia, and New Zealand. In order to investigate the possible correspondence with continental breakup, the tree with its terminal distributions was fitted to the geological area cladogram «Eurasia, North America), (Africa, (South America, Australasia») and to alternative area cladograms using the TreeFitter program. -
Arachnid Ecology in New Zealand, Exploring
1 Arachnid ecology in New Zealand, exploring 2 unknown and poorly understood factors. 3 James Crofts-Bennett. 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 “A thesis submitted in fulfilment of the degree of Master of Science [1] in Botany [2] at the 21 University of Otago, Dunedin, New Zealand” 22 2020 23 1 24 Index 25 26 Abstract………………………………………………………………………………………5. 27 Chapter 1. Introduction……………………………………………………………………...7. 28 1.1 The importance of spiders………………………………………………………...7. 29 1.2 The influence of habitat structural complexity on spider distribution and 30 abundance…………………………………………………………………………......8. 31 1.3 Invasive rodents in the context of New Zealand Araneae………………………...9. 32 1.4 Thesis structure and aims………………………………………………………..14. 33 Chapter 2. The effect of habitat structural complexity on spider abundance and diversity..15. 34 2.1 Introduction ……………………………………………………………………..15. 35 Figure 2.1: Seasonal deciduous vegetation cover…………………………...16. 36 Figure 2.2: Seasonal deciduous vegetation cover with mistletoe parasites…16. 37 2.2 Methods…………………………………………………………………………17. 38 Figure 2.3: Examples of foliage samples……………………………………18. 39 Table 2.1: Sampling locations, dates and host data…………………………19. 40 2.2.1 Statistical Analyses……………………………………………………………20. 41 2.3 Results…………………………………………………………………………...20. 42 Figure 2.4: Total invertebrates sampled in summer, plotted………………..22. 43 Figure 2.5: Total invertebrates sampled in winter, plotted………………….23. 44 Table 2.2: Paired t-tests of host plant invertebrate populations……………..25. 45 2.4 Discussion……………………………………………………………………….26. 46 Chapter 3. A novel non-kill Araneae trap: test with regards to vegetation type versus 47 location 48 effects………………………………………………………………………………………..28. 49 3.1 Introduction……………………………………………………………………...28. -
Resupinate Fungi (Basidiomycetes, Aphyllophoraies) of Macquarie Island, Australia
Hikobia 13: 745-750, 2002 Resupinate fungi (Basidiomycetes, Aphyllophoraies) of Macquarie Island, Australia GARY A. LAURSEN, HAROLD H. BURDSALL AND RODNEY D. SEPPELT LAURSEN, G. A., BURDSALL, H. H. & SEPPELT, R. D. 2002. Resupinate fungi (Basidiomycetes, Aphyllophorales) of Macquarie Island, Australia. Hikobia 13: 745-750. Fourteen collections of resupinate higher fungi in the order Aphyllophorales (Basidiomycetes) were made on Subantarctic Macquarie Island (54°30'S, 158°57' E) in 1995. Of the 14, three proved to lack species-determining characteristic basidiospores and 12 were determined to belong to three species in two genera; Athelopsis lembospora (Bourdot) Oberwinkler, Athelopsis subinconspicua (Lirschauer) Julich, the first report of this species from the Southern Hemisphere, and Epithele galzinii Bres., the first reportr of E. galzinii from an Australian territory and also representing a southern range extension by several hundred kilometers. None are endemic and all are suspected to have reached the Island by long-distance transoceanic wind dispersal from other southern continental sources. Their habitats are restricted to old and clustered culms, frond bracts, and leaf petioles of the fern Polystichum vestitum (G. Forst.) C. Presl, the raised pedestals of old giant russock grass stem bases of Poa foliosa (Hook. f-) Hook. f., and the woody, but thin, stems of Acaena magellanica (Lam.) Vahl (Rosaceae) and Coprosma perpusilla Colenso ssp. subantarcrica Orchard (Rubiaceae). Gary A. Laursen. University of Alaska Fairbanks, Institute of Arctic Biology, Fairbanks, AK 99775-6100, USA. Harold H. Burdrall, Jr.. retired Center for Forest Mycology Research, Forest Products Laboratory, Forest Service, USDA, Madison, WI 53705 USA. Rodney D. Seppelt, Australian Antarctic Division, Channel Highway, Kingston, 7050 Tasmania. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Monitoring Bactericera Cockerelli and Associated Insect Populations in Potatoes in South Auckland
Tomato-potato psyllid 269 Monitoring Bactericera cockerelli and associated insect populations in potatoes in South Auckland G.P. Walker1, F.H. MacDonald1, N.J. Larsen1 and A.R. Wallace2 1he New Zealand Institute for Plant & Food Research Limited, Private Bag 92169 Auckland 1142, New Zealand 2he New Zealand Institute for Plant & Food Research Limited, Private Bag 4704, Christchurch 8140, New Zealand Corresponding author: [email protected] Abstract Bactericera cockerelli (the tomato-potato psyllid; TPP) and associated insects were monitored weekly in unsprayed potatoes at Pukekohe by using yellow sticky traps and sampling plants from late July 2009 until mid March 2010. TPP adult catches and egg and nymphal infestations were absent or low until mid December. Other exotic and native psyllid species dominated trap catches until TPP populations increased markedly in mid January and peaked at 120 adults per trap in late February, with egg numbers reaching 520 per plant a week later. TPP nymphs peaked at 260 per plant in early February. Micromus tasmaniae (brown lacewing) was common in spring and summer, but Melanostoma fasciatum (small hover fly) became the dominant predator, peaking at 162 eggs and 35 larvae per plant in mid January. Naturally occurring predators appear to be important biological control agents of aphids, small caterpillars and probably TPP on potatoes at Pukekohe. Keywords tomato-potato psyllid, Bactericera cockerelli, sticky traps, plant sampling, potatoes, Melanostoma fasciatum, Micromus tasmaniae. INTRODUCTION Bactericera cockerelli (Sulc) (Hemiptera: Triozidae), (Liefting et al. 2009). It has been associated with most commonly known in New Zealand as foliar symptoms similar to those of zebra chip but tomato-potato psyllid (TPP), is a new invasive the insect vector in potatoes is unclear. -
Which Insect Is That-Poster-Mockup-1.Indd
Which insect is that? There are more than 20,000 species of insects in New Zealand of all shapes and sizes but most of them belong to only five groups or “Orders”. Even if different insects in an order look very different, they all share a few important similarities. Beetles Ants & Bees Butterflies & Moths Flies True Bugs Coleoptera Hymenoptera Lepidoptera Diptera Hemiptera Beetles are known as Coleoptera (from the Greek koleos The Hymenoptera include ants, wasps and bees. The Lepidoptera includes moths and butterflies of We usually think of flies as pests but they are hugely Hemiptera means half-wing (from the Greek hemi “half” “sheath” + pteron “wing”), which refers to how their first Some of the members of this order are hugely important which there are 2,000 native species in New Zealand. Moths important for pollination and breaking down rotting + opteron “wing”). This is because the first pair of wings pair of wings have hardened into an “elytra” which covers the as pollinators, predators or pests. In this group, the front are usually active during the night and are usually less material. Most insects have two pairs of wings but in some is hardened at the base while part of the wing is thin and second pair of wings (and usually the entire abdomen) as a and hind wings are locked together by a tiny row of hooks colourful than butterflies, but there are exceptions. If you’ve cases one pair will be modified to perform another function. membranous. Entomologists refer to insects in this order as protective case. -
Pollination in New Zealand
2.11 POLLINATION IN NEW ZEALAND POLLINATION IN NEW ZEALAND Linda E. Newstrom-Lloyd Landcare Research, PO Box 69040, Lincoln 7640, New Zealand ABSTRACT: Pollination by animals is a crucial ecosystem service. It underpins New Zealand’s agriculture-dependent economy yet has hitherto received little attention from a commercial perspective except where pollination clearly limits crop yield. In part this has been because background pollination by feral honey bees (Apis mellifera) and other unmanaged non-Apis pollinators has been adequate. However, as pollinators decline throughout the world, the consequences for food production and national economies have led to increasing research on how to prevent further declines and restore pollination services. In New Zealand, managed honey bees are the most important pollinators of most commercial crops including pasture legumes, but introduced bumble bees can be more important in some crops and are increasingly being used as managed colonies. In addition, New Zealand has several other introduced bees and a range of solitary native bees, some of which offer prospects for development as managed colonies. Diverse other insects and some vertebrates also contribute to background pollination in both natural and agricultural ecosystems. However, New Zealand’s depend- ence on managed honey bees makes it vulnerable to four major threats facing these bees: diseases, pesticides, a limited genetic base for breeding varroa-resistant bees, and declining fl oral resources. To address the fourth threat, a preliminary list of bee forage plants has been developed and published online. This lists species suitable for planting to provide abundant nectar and high-quality pollen during critical seasons. -
Interactive Effects of Climate Change and Species Composition on Alpine Biodiversity and Ecosystem Dynamics
Interactive effects of climate change and plant invasion on alpine biodiversity and ecosystem dynamics Justyna Giejsztowt M.Sc., 2013 University of Poitiers, France; Christian-Albrechts University, Germany B. Sc., 2010 University of Canterbury, New Zealand A thesis submitted to Victoria University of Wellington in partial fulfilment of the requirements for the degree of Doctor of Philosophy School of Biological Sciences Victoria University of Wellington Te Herenga Waka 2019 i ii This thesis was conducted under the supervision of Dr Julie R. Deslippe (primary supervisor) Victoria University of Wellington Wellington, New Zealand And Dr Aimée T. Classen (secondary supervisor) University of Vermont Burlington, United States of America iii iv “May your mountains rise into and above the clouds.” -Edward Abbey v vi Abstract Drivers of global change have direct impacts on the structure of communities and functioning of ecosystems, and interactions between drivers may buffer or exacerbate these direct effects. Interactions among drivers can lead to complex non-linear outcomes for ecosystems, communities and species, but are infrequently quantified. Through a combination of experimental, observational and modelling approaches, I address critical gaps in our understanding of the interactive effects of climate change and plant invasion, using Tongariro National Park (TNP; New Zealand) as a model. TNP is an alpine ecosystem of cultural significance which hosts a unique flora with high rates of endemism. TNP is invaded by the perennial shrub Calluna vulgaris (L.) Hull. My objectives were to: 1) determine whether species- specific phenological shifts have the potential to alter the reproductive capacity of native plants in landscapes affected by invasion; 2) determine whether the effect of invasion intensity on the Species Area Relationship (SAR) of native alpine plant species is influenced by environmental stress; 3) develop a novel modelling framework that would account for density-dependent competitive interactions between native species and C.