I' % i ■iV iji' 't: ' ■;V H;, ( THE Entomologist’s Record AND Journal of Variation Edited by C.W. PLANT, B.Sc., F.R.E.S. CONTENTS AND SPECIAL INDEX Vol. 119 2007 ISSN 0013-8916 THE ENTOMOLOGIST’S RECORD AND JOURNAL OF VARIATION World List abbreviation: Entomologist’s Rec. J. Van http://www.entrecord.com Editor C.W. PLANT, B.Sc., F.R.E.S. 14 West Road, Bishops Stortford, Hertfordshire CM23 3QP. Telephone/Facsimile: 01279 507697 E-mail: cpaukI@ntlworld.com Registrar Treasurer R.F. McCormick, f.r.e.s. C.C. Penney, f.r.e.s. 36 Paradise Road, 109 Waveney Drive, Springfield, Teignmouth, Devon TQM SNR Chelmsford, Essex CM I 7QA WHERE TO WRITE EDITOR: All material for publication, including books for review and advertisements REGISTRAR: Changes of address TREASURER: Subscriptions and non-arrival of the Journal Readers are respectfully advised that the publication of material in this journal does not imply that the views and opinions expressed therein are shared by the Editor, the Entomologist’s Record Committee or any party other than the named author or authors. Entomologist's Record and Journal of Variation is a non profit-making journal, funded by subscription, containing peer-reviewed papers and shorter communications. It is published by the Entomologist’s Record Committee, comprising the Editor, the Registrar and the Treasurer, from the Editorial address. An Editorial Advisory Panel exists to assist the Editor in his work. The annual subscription for year 2007 is £28 for individual subscribers or £50 for institutions. INSTRUCTIONS TO CONTRIBUTORS • This journal publishes peer-reviewed papers and shorter Notes that are reviewed by the Editor. Contributions are accepted on merit, with no regard whatsoever to the occupation or standing of the author. All contributions should bear the name and postal address of the author(s), but titles or honours are not permitted and will be removed. One e-mail address may also accompany the contribution. First time authors and non-subscribers are welcome to send material for publication. We are able to include colour photographs from time to time at no cost to the author(s). Good quality monochrome photographs are always welcomed. • The journal is concerned with British Lepidoptera (moths and butterflies). We also accept contributions on British Coleoptera (beetles), British Diptera (flies) and other groups at the Editor’s discretion. 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Papers must cover their subject matter to a far greater depth than Notes and should present original material or a broad-based review of existing knowledge. Descriptions of new species may be submitted. Authors of papers are expected to follow the house style and conventions as closely as possible. The Editor reserves the right to convert papers into Notes. • Notes are the meat of the journal! Most contributions will fall into this category. They will normally be less than 1500 words in length and can be very short indeed as long as the information they impart is interesting. We welcome Notes. There is no limit to how many you can contribute. Authors of Notes should try as far as possible to follow the house style and conventions, but the Editor will attend to these if errors are made. • We accept all formats from hand-written notes upwards. However, we prefer submissions via e-mail, or on CD. Files must be in a PC-compatible format that is readable by Microsoft Word. Originals are required for all photographs, drawings, diagrams, graphs, histograms and similar, though Tables may be incorporated into word processor files. For details, visit the web site or contact the Editor direct. CONTENTS compiled by Colin W. Plant and Andrew Smith 1: PEER-REVIEWED PAPERS B Bucculatrix Ulmifoliae M. Hering, 1931 (Lep.: Bucculatricidae) resident in England. John R. Langmaid, Jim Porter and Graham A. Collins, 195-201 Butterflies on farmland: The first 10 years of recording at Writtle College. R. G Field and T Gardiner, 49-56 c Clepsis coriacana (Rebel, 1894) (Lep.: Tortricidae) new to Britain. David Manning, 235-237 D (The) distribution, ecology and conservation of the Lunar Yellow Underwing Noctua orbona (Hufnagel) in the Breck District of Norfolk and Suffolk. M. S. Parsons and G.M. Haggett, 203- 211 (The) Double Line Mythimna turca (L.) (Lep.: Noctuidae): notes on its habitats, foodplants and suggested management in England and Wales. R. J. Wolton, A. Spalding and B. P Henwood, 133-142 (The) dwarf form of Silver Y Autographa gamma (L.) (Lep.: Noctuidae). Roy Leverton, 103-107 E Eupeodes goeldlini (Dip.: Syrphidae) new to Britain, France and Ireland, with a key to separate it from related Atlantic zone species. Martin C. D. Speight, Jean-Pierre Sarthou and David A. Levy, 213-219 I (The) immigration of Lepidoptera to the British Isles in 2003. Sean Clancy and Bernard Skinner, 1-41 (The.) immigration of Lepidoptera to the British Isles in 2004. Sean Clancy, 145-184 M Microlepidoptera Review of 2006. J. R. Langmaid and M. R. Young, 241-266 N Nineta pallida (Schneider, 1846) (Neu.: Chrysopidae), a lacewing new to the British Isles. Martin C. Harvey and Colin W. Plant, 77-82 P Parna apicalis (Brischke, 1888) (Symphyta: Tenthredinidae), a Leaf-mining Sawfly new to Great Britain. Rob Edmunds, Steve Hind, Andrew Liston and Keith Palmer, 223-226 Pine-tree Lappet Dendrolimus pini (L.) (Lep.: Lasiocampidae) possibly resident in Scotland. Roger Kiddie, 231-233 iii R Resting postures of Large Yellow Underwing Noctua pronuba ([L.], Lep.; Noctuidae) final instars. Michael A. Dockery, 267-273 Rhaphium nasutum (Diptera: Dolichopodidae), Pherbellia rozkosnyi & Tetanocera montana (Dip.: Sciomyzidae), insects new to Ireland and Geomyza balachowski (Dip.: Opomyzidae), presence in Ireland confirmed. Martin C. D. Speight, 85-91 (The) rise of the Scarce Bordered Straw Helicoverpa armigera (Hiibner) (Lep.: Noctuidae). M.S. Parsons & P Davey, 185-192 s Sericomyia hispanica Peris, a little-known European Hoverfly (Dip.: Syrphidae) recorded for the first time from the French Pyrenees. Martin C. D. Speight, 109-11 1 u Uresiphita reversalis (Guence, 1854) (Lep.: Pyralidae) new to Britain and Europe. Tony Davis and Doug Miller, 59-61 w Water Betony Shargacucullia scrophulariae (D. & S.) (Lep.: Noctuidae) new to the Channel Islands. Philip H. Sterling and Peter D. M. Costen, 97-102 2: NOTES A Acleris lipsiana (D.&S.) (Tortricidae) and Eudonia lineola (Curtis) (Pyralidae) new to the Shetland Isles. Jon Clifton, 45 Acleris logiana (Cl.) (Lep.: Tortricidae) on Guernsey. P. D. M. Costen, 44 Additional evidence supporting the migration of Cornifrons ulceratalis Lederer (Lep.: Crambidae, Evergestinae) in the Mediterranean region in October 2006. Martin R. Honey Inmaculada Ferriz & Nick J. Riddiford, 237-238 Additional notable British barkfly (Psocoptera) observations. R. (Bob) E. Saville, Keith N. A. Alexander, John H. Bratton, Laurence Clemons and G. Marcus E. Oldfield, 113-115 (The) advantages of Doing the Dirt: New and interesting moth records for Hertfordshire & Middlesex. Rachel Terry, 62-63 An invasion of the Harlequin Ladydird (Harmonia axyridis Pallas) (Col. Coccinellidae) in the South Wight. Sam Knill-Jones, 82 Atlantopsocus adustus (Hagen) (Psoc.: Psocidae) new to Britain from East Cornwall. Keith N. A. Alexander, 76 Atlantopsocus adustus (Hagen) (Psoc: Psocidae) new to Britain from East Cornwall a correction. Keith N. A. Alexander, 234 Avian predation of Sand Dart agrotis ripae Hb. (Lep.: Noctuidae). Roy Leverton, 46 B Bloxworth Snout Hypena obsitalis (Hb.) (Lep.: Noctuidae) hibernating in German wartime bunkers on Guernsey and Alderney. P D. M. Costen, 116-118 IV c Calophasia lunula Hufn. (Lep.: Noctuidae) in north-west Kent in 2007. B. K. West, 287 Caterpillars drinking sugar. Roy Leverton, 44 Coleophora involucrella (Chrtien, 1905) (Lep.: Coleophoridae): The second record for France. Jon Clifton, 111-112 Coleophora squamosella Stainton (Lep.: Coleophoridae), new to the Hertfordshire (VC20) county list. Philip J. L Gould, 202 Colonies of the Asian elm aphid Tinocallis takachihoensis Higuchi (Hem.: Aphididae) in Britain. Thomas F Doring, 226-227 (A) colony of Deltote bankiana (Fabr.) (Lep.: Noctuidae) persisting on a calcareous downland site in East Kent (VC 15). Sean Clancy, 112 Confirmation of the hybrid status of the Autumnal Snout Schrankia intermedialis Reid (Lep.: Noctuidae). Philip J. L. Gould, 193-194 Cornifrons ulceratalis (Lederer, 1858) (Lep.: Crambidae) new to France and Syncopacma albifrontella (Heinemann, 1870) (Lep.: Gelechiidae): first published French record. Michael & Brenda Marney, 56-58 Could the Spanish Character Cilix hispanica De-Gregorio, Torruella, Miret, Casas & Figueras, 2002 (Lep.: Drepanidae) be overlooked in the British fauna? Colin W. Plant, Michael Marney and Graham Wenman, 194 Craniophora ligustri D.&S. (Lep.: Noctuidae): from rarity to population explosion at Dartford, Kent and melanism. B. K. West, 92-94 D Diaperis boleti (L.) (Col.: Tenebrionidae) in Hatfield Forest, Essex. Ross Piper, 74-75 Diaperus boleti (L.) (Col.: Tenebrionidae) not confined to birch polypore fungus. Keith N. A. Alexander, 108 E Ectoedemia heringella (Mariani). (Lep.:Nepticulidae) a first record for North Hampshire (VC 12). Rob Edmunds, 202 F (A) fourth Hertfordshire (VC20) record of the Apple Pith Moth Blastodacna atra (Haworth) (Lep.: Agonoxenidae). Philip J. L. Gould, 212 H Hazards of butterfly collecting. It seemed a good idea at the time: London 2001. Torben B. Larsen, 42-43 Hazards of butterfly collecting: Paragliding butterflies Ghana 2007. Torben B. Larsen, 118-120 Hazards of butterfly collecting: Revisiting Boabeng-Fiema Ghana 2007. Torben B. Larsen, 283- 285 Hazards of butterfly collecting: The lifeline that is the BBC World Service the World, 1970-2007. Torben B. Larsen, 22 1 -222 Hazards of butterfy collecting. Bumbuna Butterfly Survey Sierra Leone, May 2006. Torben B. Larsen, 65-67 Hummingbird Hawk-moth Macroglossum stellatarum (L.) (Lep.: Sphingidae) caterpillars in Banffshire. Levertow, 108 V I I married a Moth Man a warning to new moth spouses. Pat Costen, 68-71 L Late-flying Silver-ground Carpets Xanthorhoe montanata D. & S. (Lep.; Geometridae) in Banffshire. Roy Leverton, 63 Lepidoptera new to the Isle of Wight in 2006. Sam Knill-Jones, 67-68 M Moths and moth recorders in Lancashire a changing scene. Stephen Palmer, 277-282 N (A) naturalised population of a Mediterranean earwig, Forficula puhescens Gen (Derm.: Forficulidae) in West Sussex. John Paul, 83-84 Nest building and prey stocking in Crossocenis megacephalus (Rossius) (Hym.: Sphecidae). Ross Piper, 58 News on the conservation of some moths listed in the UK Biodiversity Action Plan and two additional British Red Data Book species. Paul Waring, 124-132 Notes on the early stages of Elachista regificella Sircom, 1849 and E. tengstromi Kaila et al, 200 1 . John R. Langmaid, 64-65 P Pale Shining Brown Polia bomhycina (Hufn.) (Lep.: Noctuidae) re-discovered in Oxfordshire in 2005 and 2006 a nationally significant population of a UK Biodiversity Action Plan Priority Species. Martin C. Townsend and Thomas MercLx, 11-1 A (The) Pale-shouldered Cloud Chloantha hyperici (D. & S.) (Lep.: Noctuidae) in North London: Sixth British record. Geojfrey Geiger, 143 Perils of the vernacular A. A. Allen, 46 R Recent changes in the distribution and status of the Toadflax Brocade Calophasia lunula (Hufn.) (Lep.: Noctuidae) in Britain. Tim Freed, 274-276 Red Admiral Vanessa atalanta (L.) (Lep.: Nmyphalidae) courtship in winter. Richard Fox, 75-76 (A) Red Admiral Vanessa atalanta L. (Lep.: Satyridae) in London on the first of March. Torben B. Larsen, 107 Remms Rustic Mesaparnea remmi (Rzbnyai-Reser) (Lep.: Noctuidae) on Guernsey. P. D. M. Costen, 233-234 (The) Rothamsted Insect Survey light trap on Jersey species of note in 2004. Philip J. L. Gould, 220 s Scarce Tissue Rheumaptera cervinalis (Scop.) (Lep.: Geometridae): a new record for north-east Scotland. N. Picozzi, 229-230 Scotch Annulet Gnophos obfuscatus (D. «fe S.) (Lep.: Geometridae) on a pebble beach. Roy Leverton, 123 Scythris potentillella (Zeller) (Lep.: Scythrididae) new to Hertfordshire. David Murray, 71 (The) Small Chocolate-tip Clostera pigra (Hufn.) (Lep.: Notodontidae) in Kent. Philip J. L. Gould, 286 VI Small Ranunculus Hecatera dysodea (D.&S.) (Lep.: Noctuidae) reaches Bristol. Steve Freddy, 276 Stauropoctonus bombycivorus (Gravenhorst) (Hym.: Ichneumonidae) new to the Isle of Wight. Sam Knill- Jones, 45-46 T Third British record of Uloma culinaris (L.) (Col.: Tenebrionidae) from southern Hertfordshire. D. Murray, 44-45 Tilia cordata a new foodplant for Incurvaria pectinea Haw. (Lep: Incurvariidae). Rob Edmunds, 228-229 Tomoxia bucephala Costa (Col.: Mordellidae): A case of long persistence in the same locality. A. A. Allen, 94 X Xanthia icteritia Hufn. (Lep.: Noctuidae): A comment on infraspecific variation, especially in regard to Kent B. K. West, 121-122 3: SUBSCRIBERS’ NOTICES, ANNOUNCEMENTS etc Atlantoraphidia macuUcollis required. Prof. Dr Horst Aspock, 47 Corrigendum, 288 European invertebrates. Petr Kell, 94 MOTHS COUNT and the National Moth Recording Scheme an update. Zoe Randle, 122-123 4: BOOK REVIEWS Ecology of an almost extinct population of the Scarce Swallowtail IphicUdes podalirius (Linnaeus, 1758) by R. Steiner, G. Hermann & J. Settele, 240 Ecology, Phenotypes and the Mendelian Genetics of Burnet Moths (Zygaena Fabricius, 1775) by W. Gerald Tremewan, 96 Guide des papillons nocturne de France edited by Roland Robineau, 287-288 Moths of Europe, Volume 1: Saturnids, Lasiocampids, Hawkmoths and Tiger Moths by Patrice Leraut, 47-48 Pyraloidea of Europe/Europas ( Lepidoptera) Volume/Band 1: Pyralinae, Gelleriinae, Epipaschiinae, Cathariinae and Odontiinae by F. Slamka, 95-96 Studies on the ecology and conservation of butterflies in Europe. Volume 1 General concepts and case studies and Volume 2 Species ecology along a European gradient: Maculinea butterflies as a model, 240 The Lepidoptera of Israel edited by G.C. Mller, V.D. Kravchenko, A. Hausmann, W. Speidel, J. Mooser & T.J. Witt and Volume 2: Noctuidae by V.D. Kravchenko, M. Fibiger, A. Hausmann & G.C. Mller, 239-240 vn CONTRIBUTORS Page number entries in bold type refer to peer-reviewed papers; entries in ordinary type refer to notes and shorter communications that have been refereed internally by the editor and his colleagues. Where an author is not the first named of multiple authors, the page number entry is printed in italic type. Alexander, K. N. A. 76; 108; 113-115; 234 Allen, A. A. 46; 94 Aspock, H. 47 Bratton, J. H. 1I3-II5 Clancy, S. 1 -41; 112; 145-184 Clemons, L. 113-115 Clifton, J. 45; 111-112 Collins, G. A. 195-201 Costen, Pat. 68-71 Costen, P. D. M. 44; 97 - 102; 116-118; 233-234 Davey, P. /«5-/92 Davis, T 59 - 61 Dockery, M. A. 267 - 273 Doring, T. F. 226-227 Edmunds, R. 202; 223 - 226; 228-229 Ferriz, I. 237-238 Field, R. G. 49 - 56 Fox, R. 75-76 Freed, T. 274-276 Gardiner, T. 49 - 56 Geiger, G. 143 Gould, P. J. L. 193-194; 202; 212; 220; 286; Haggett, G. M. 203 - 211 Harvey, M.C. 77-82 Hind, S. 223 - 226 Honey, M. R. 237-238 Keil, P. 94 Knill-Jones, S. 45-46; 67-68; 82 Langmaid, J. R. L 64-65; 195 - 201; 241 - 266 Larsen, T. B. 42-43; 65-67; 107; 118-120; 221- 222; 283-285 Leverton, R. 44; 46; 63; 103 - 107; 108; 123; Levy, D. A. 213 - 219 Liston, A. 223 - 226 Marney M. 56-58; 194 Marney, B. 56-58 Merckx, T. 72-74 Miller, D. 59 - 61 Murray, D. 44-45; 71 Nenwood, B. P. 133 - 142 Oldfield, G. M. E. 113-115 Palmer, S. 277-282 Palmer, K. 223 - 226 Parsons, M. S. 185 192; 203 - 211 Paul, J. 83-84 Picozzi, N. 229-230 Piper, R. 58; 74-75 Plant, C.W. 77-82; 194 Porter, J. 195 - 201 Preddy, S. 276 Randle, Z. 122-123 Riddiford, N. J. 237-238 Sarthou, J.- P. 213 - 219 Saville, R.E. 113-115 Skinner, B. 1-41 Spalding, A. 133 - 142 Speight, M. C. D. 85-91; 109 - 111; 213 - 219 Sterling, P. H. 97 - 102 Terry, R. 62-63 Townsend, M. C. 72-74 Waring, R 124-132 Wenman, G. 194 West, B. K. 92-94; 121-122; 287 Wolton, R. J. 133 - 142 Young, M. R. 241 - 266 SPECIAL INDEX Compiled by Catherine Wellings Newly described taxa are indexed in bold type Taxa new to, or newly recognised in, the British Isles and mentioned first in this volume are denoted by an asterisk. Page Page LEPIDOPTERA angelicella, Agonopterix.. 253 abceps, Apamea. ....... ............. ................279 angustea, Eudonia ........... .........262 abietaria, Eupithecia 14 angustella, Nephopterix... ...11,265 abietella, Dioryctria........ ...11,265 annadactyla, Stenoptilia .. 266 abscisana, Lobesia. ..259, 280 antiopa, Aglais ...13, 155 absinthii, Cucullia 278 apicipunctella, Elachista . 252 acanthadactyla, Amblyptilia .. 280 argentimaculella, Infurcitinea 246 accaiis, Diasemia................... ..152 argiolus, Celastrina ...53 acetosae, Enteucha 245 armigera, Helicoverpa (= Heliothis). .1,35, acroxantha, Tachystola .278, 280 146, 147, ] ill, 185-192, 282 acuminatana, Dichrorampha. ..261 asiatica, Cilix 194 acutellus, Scierocona. ............ 3, 8, 152 asiatica, Nycteola ...2, 3,21 adelphella, Sciota ..11, 154, 264 aspersana, Acleris 258 adjunctella, Coleophora 251 assectella, Acrolepiopsis.. 7, 149, 250 adspersella, Coleophora........ 251 assimilella, Stigmella....... .........244 adustata, Ligdia 220 astrantiae, Agonopterix ... ....253 advenella, Trachycera 264 atalanta, Vanessa. ...26, 53,15-16, 107, 171 aegeria, Pararge.. ....... ........... ......51,53, 54 atra, Acanthopsyche .........246 aeneana, Commoph ila.... 128 atra, Blastodacna..... 212 aeneofasciella, Stigmella 244 atricapitana, Cochylis...... 257 aequidentellus, Epermenia .... .262 atricollis, Ectodemia .........244 aeriferanus, Ptycholomoides . ..257 atricomella, Elachista...... ..252 aerugula, Nola 3, 18, 160 atrifrontella, Ectodemia... ..244 aestimaria, Chiasmia..... 146, 156 atriplicis, Trachea ....3, 20, 146, 164 ajfinis, Bryotropha....... 254 atropos, Acherontia.. ..14, 37, 147, 156 ajfinis, Cosmia 131 augur, Grapholita 278 agestis, Aricia ............51,53 aurantia ab. of icteritia, Xanthia .. 121 alacella, Dichomeris ..........255 aurata, Pyrausta ..263 alhedinella, Biicculatrix ...195-200 auriferella, Stathmopoda . .242, 256 albicilla, Salebriopsis 264 aurita, Pammene. .261 albicosta, Coleophora. ................251 aurota, Belenois ............... .........118 albidella, Coleophora 68,250 autumnaria, Ennomos ...14, 156 albifrontella, Syncopacma 56-58 autumnitella, Acrolepia.... ,250, 280 albimaculea, Denisia ............. ..252 azaleella, Caloptilia ,247, 281 albipuncta, Mythimna 18, 162 badia, Anatrachyntis .........150 albovenosa, Simyra 20 badiella, Depressaria 253 albuginana, Pammene ........... ..260 bankesiella, Epischnia ..... 265 albula, Meganola ..18, 130, 160 bankiana, Deltote 20, 112, 165 albulata, Asthena.... .220 bechsteinella, Bucculatrix 247 algae, Cryphia.. 20, 146, 164, 220, 274 berberata, Pareulype .124-126 algira, Dysgonia ..67, 147, 166 betulae, Parornix ....247 algirica, Cilix... 194 betulina, Proutia. 246 alpella, Ypsolopha ................249 bidentata, Odonoptera..... 44 alpinella, Platytes 151 bifasciana, Spatalistis...... 258 alpium, Moma 220 bifractella, Apodia 253 ambigualis, Scoparia..... 262 bigella, Euzophera ....2, 11, 147, 154 amhiguella, Eupoecilia... ....7, 150, 257 bilunana, Epinotia .........259 amplana, Cydia 7, 146, 150, 179, 261 bimaculata, Lomographa. 280 anachoreta, Clostera 17, 37 binaevella, Phycitodes ..... 265 IX binotella, Hypatoga ....242, 255 bipunctata, Scotopteryx 277 bipunctella, Ethmia 7, 149 biriviata, Xanthorhoe. 14 bistrigella, Phylloporia 245 biviella, Vitula ........12, 154, 242, 265 blandella, Caryocolum 255 boeticus, Lampides 13, 37 boisduvaliella, Pima 11 bombycina, Polia ...18, 72-74 boreella, Bryotropha..... 254 botrana, Lobesia 63 bractea, Autographa 22 bractella, Oecophora 252 brassicae, Pieris 53, 154 britanniodactyla, Capperia. 266 brongniardella, Acwcercops.. 28 1 brunnichana, Epinotia 259 brunnichella, Stephensia..... 25 1 caecimaculana, Pelochrista 260 caespititiella, Coleophora 25 1 cagnagella, Yponomeuta 6 caja, Arctia 193, 278 c-album, Polygonia....... ...51, 53, 54 caliginosa, Acosmetia 1 30 calodactyla, Platyptilia 266 calthella, Micropterix 243 campoUUana, Eucosma 260 canella, Gynmancyla 265 caniola, Edema 17, 159 caprana, Epinotia 62, 259 capsica, Bucculatrix 196 cardamines, Anthocharis 51, 53, 54 cardui, Cynthia .....51, 53 cardui, Vanessa 1, 3, 26, 171 catalaunalis, Antigastra ..............263 cautella, Ephestia 12 cephalonica, Corey ra 264 cerago ab. of icteritia, Xanthia 121, 122 cerasicolella, Phyllonorycter 248 cervinalis, Rheumaptera 124, 229-230 cespitana, Celypha..... 258 cespitis, Tholera 278 chaerophyllella, Epermenia .261 chalcites, Chrysodeixis .......21, 146, 165 Charaxes 120 chlamitulalis, Nola.... ....146, 160 chlorana, Earias ....21 choragella, Morophaga ....246 chrysippus, Danaus.. 67 chrysorrhea, Euproctis 17 cicadella, Scythris.... 256 cicatricella, Haimbachia 3, 7, 146, 151 cidarella, Bucculatrix ....247 cilium, Spodoptera....... ............238 cinerosella, Euzophera ....265 cingulata, Pyrausta.. 263 cinnamomella, Ancylosis 2, 3, 11 circumvoluta, Myelois. .....265, 280 citrella, Phyllocnisits 149 citri, Prays ..........249 clathrata, Chiasmia ........14, 156 claustrella, Bacotia 246 cloacella, Nemapogon 246 clypeiferella, Coleophora 251 cnicana, Aethes 257 columbariella, Tinea 246 combinella, Pseudoswammerdamia. 249 comes, Noctua 272 confusa, Macdunnoughia 22, 38, 166, 180, 181 congressariella, Nothris. ..99, 149 conicolana, Cydia .62, 261 conjuncta, Catocala.... ..146, 167 consimilana, Clepsis 236 consortella, Cosmiotes 252 conspersana, Cnephasia 258 conspicuella, Coleophora 1 1 1 conterminana, Eucosma 260 convolvuli, Agrius. .....1, 4, 29-30, 173 conyzae, Coleophora 250 coracipennella, Coleophora ...250 coriacana, Clepsis * 235-237, 242, 257 coronata, Phlyctaenia 263 coronula ab. ofligustri, Craniophora, 92-94 coryli, Phyllonorycter.............. .........248 cosmophorana, Cydia.... 261 costaestrigalis, Schrankia. ..59, 193 costalis, Hypsopygia ...264 crassa, Agrotis .......3, 18, 160 crataegella, Scythropia.. 249 crataegi, Trichiura....... 278 crenata, Gluphisia .2, 3, 17, 180 crepusculella, Pseudopostega ................ 245 cristana, Acleris.. 258 cristatella, Bucculatrix ..........247 croceus, Colias 25, 51, 53, 170, 189 crocicapitella, Monopis 246 cruciana, Epinotia ........................259 crypt ella, Trifurcula 244 cuculipennella, Caloptilia 247 cultraria, Watsonalla .....280 cuprella, Adela ...........245 cupressata, Thera......... .....14, 156 cupressella, Argyresthia. .62, 249 cursoria, Euoxia 38, 180, 111 curvatula, Drepana 3, 13, 155, 180 curvipunctosa, Agonopterix 253 cyaneimarmorella, Stenoptinea 242, 246 cynosbatella, Epiblema 260 cytisella, Monochroa 253 X damocles, AmaMm.. ............................ .....67 daplidice, Pontia. 13 dardoinaria, Crocallis 180 daucella, Depressaria ..252 deauratella, Coleophora .250 decentella, Ectoedemia.. 244, 280 deceptoria, Deltote ............38 degeneraria, Idaea .....155 demarniana, Epinotia.. 259 dentella, Phaulernis..... 261 depressa, Eilema. 280 desertella, Bryotropha .254 didyma, Mesapamea. .................... ..233=234- diffinis, Cosmia. ......... ................ ....130, 277 diffinis, Teleiopsis ....71 dilectella, Argyresthia 249 diminutana, Ancylis 259 discordella, Coleophora .....251 dispar, Lymantria.... 3, 17, 159 distinctella, Chionodes ..........................254 diversana, Choristoneura 257 divisella, Mompha .256 dodecea, Ethmia 7, 149, 253 domestica, Bryotropha ..254 dorninula, Callimorpha. 160 drurella, Chrysoesthia ..254 dubiella, Tinea 246 dubitata, Triphosa 117 duplicella, Narycia 246 dysodea, Hecatera 276, 282 effractana, Acleris .........242, 258 electa, Catocala .........38, 146, 167, 180 emargana, Ancyclis. ...... ............. ............ 242 emberizaepenella, Phyllonorycter 248 emkopoti, Anthene 221 emortualis, Trisateles. 22 ephemerella, Acentria.... ..262 eriphia, Antichloris 2, 18, 67 erythrocephala, Conistra.....4, 19, 146, 163 euphorbiae, Hyles.......... 3, 15, 157 evonymella, Yponomeuta 6, 149 exigim, Spodoptera 1, 2, 3, 34, 145, 177, 238 exsiccata, Tathorhynchus 146, 167, 180 exsoleta, Xylena..... .................4, 19, 277 extimalis, Evergestis ...............8, 151 extrema, Chortodes ..164 fagiglandana, Cydia 261 falacella, Scythris ...278 falciformis, Epermenia 261 fallax, Elegia 37 falsella, Catoptria.... ..........262 farinalis, Pyralis 264 fascelinella, Pediasia. ..........8, 151 fasciella, Nemophora... ..245 ferchaultella, Luffia 246 ferrugalis, Udea... 24, 38, 59, 147, 169, 263 festaliella, Schreckensteinia. .................. 262 figuiilella, Ephestia. 154, 180 filicivora, Psychoides....... 246, 281 flammea, Mythimna 163 flammea, Trigonophora 4, 19, 163 flammealis, Endotricha.. 264 flavescens ab. oficteritia, Xanthia 121, 122 flaviciliana, Cochylis 257 flavicincta, Polymixis 282 flavidorsana, Dichrorampha 261 flavipennella, Coleophora ....250 flexula, Lespeyria ........282 fluxa, Chortodes... ........20 foenella, Epiblema... .......260 forficalis, Evergestis .263 forficella, Donacaula 262 formosa, Pempelia 264 formosana, Enarmonia 260 formosanus, Lozotaeniodes... 257, 281 forsskaleana, Acleris.... .....258 forsterella, Glyphipterix 248 fovealis, Duponchella ...... \0, 152, 264, 281 fraternana, Epinotia 259 fraxini, Catocala 4, 22, 38, 166 fuliginaria, Parascotia. 22, 167, 282 fuliginosa, Phragmatobia ..........44 fulvago ab. oficteritia, Xanthia 121, 122 fulvalis, Udea. 9 fumatella, Chionodes 254 funebrana, Grapholita 261 furfurana, Bactra ..259 fusca, Pyla........................ ....265 fuscatella, Lampronia....... 245 gallicana, Pammene 261 gallii, Hyles 15, 157, 180 gamma, Autographa 36, 59, 103-107, 168, 179 gammina var. of gamma, Autographa.. 103- 107 gemmella, Stenolechia ......254 geniculea, Agriphila ...262 genitalana, Cnephasia 258 geryon, Adscita 278 gibbosella, Psoricoptera 254 gilvago, Xanthia... ............20 gilvaria, Aspitates 112 gilvata, Uresiphita 59, 60 gilvicomana, Phalonidia 257 glabratella, Argyresthia...... .....249, 266 glaucata, Cilix .....194 glaucicolella, Coleophora ..................... 25 1 globulariae, Jordanita ....112 glutinosae, Stigmella 245 gnidiella, Cryptoblabes..... 11 goedartella, Argyresthia 249 gonodactyla, Platyptilia 266 gorganus ssp. ofmachaon, Papilio .......180 grandaevana, Epiblema................. .150 XI grandipennis, Scythris ...........................256 grandis, Schijfermuellerina ...................252 graslini, Agrotis ..................................... 180 griseata, ............................. 209 grisella, Achroia ....................................264 griseola, ................................... 282 grossulariata, AZ?raxM5..... ..................... .278 grossulariella, Zop/ioJia.......... ............. .265 grotiana, Epagoge .................................257 gueneeana, Dichrorampha ....................261 gularis, Paralipsa ................. .....W, 63, 153 gysseleniella, Cedestis ...................... .....2A9 hamana, Agapeta ...................................251 hannoverella, Ectodemia ............. ..........2AA harpagula, Sabra...........................l2A, 132 hastata, Rheumaptera.. .......................... 211 heparana, Pandemis ..............................251 hepariella, Zelleria ................................249 heringella, Ectodemia. ............... ....292, 244 herrichiana, Fammewe... ...................... ..261 hesperica ssp. of leautieri, Lithophane, ..19 hexadactyla, Alucita. ............... ....... 116, 117 hispanica, Cilix.. ............................... .....\9A histrionana, Dichelia.... ....2, 7 hornigi, Monochroa.. 253 horridella, Ypsolopha. 249 hortulata, Eurrhypara....... ................263 hospes, Proxenus {-Athetis) ...........2, 3, 4, 20, 67, 146, 164 hostilis, S'doto.......... ............ .................. 154 hyale, Colias .......................................... 154 hyperantus, Aphantopus ....................51, 53 hyperici, Chloantha {= Actinotia).........2, 3, 20, 143, 147, 164 ibipennella, Coleophora ........................25 1 icarus, ......................... ...53 icteritia, Xanthia.............................\2\-122 ignorata, Pammene.......... ............ ..2A2, 260 illutana, Cydia ........................ ...............26\ imbecilla, Eriopygodes .................. \2A, 131 imitaria, Scopula...... .............................. 2^0 immaculatella, Eulamp rotes .................. 253 imperfecta ab. of icteritia, Xanthia..... ...121 impluviata, Hydriomena ........................220 incertana, Cwep/ia^ia...... ....................... 258 inspersella, Scythris......... ...................... 256 insulana, Farias.. ................................. ..238 intermedialis, Schrankia.. ...............193=194 interpunctella, Plodia ............................265 interrogationis, Syngrapha .................... 1 66 intricata, Eupithecia ..............................282 involucrella, Coleophora.... ......... ...1\\-112 io, Inachis....... ....................... .....53, 5A, 116 ipsilon, Agrotis.........................32, 145, 174 irrorrella, Ypnomeuta.... ....... ..............1 , 149 italica, Metalampra ...............2, 1, 149, 252 janthina, Noctua 2, 3, 18, 68, 146, 160, 180 josephinae, Pseudatemelia ....................252 jungiella, Grapholita .............................261 jurtina, Maniola......... ....... ...........5\, 53, 54 kadenii, Platyperigea............2, 3, 4, 20, 38, 146, 164, 180 koerneriella, Incurvaria.................22K, 229 kuehniella, Ephestia........ ................ ......... 12 labdaca, Libythea .................................. 120 labecula, Dryobota ................................ 163 laburnella, Leucoptera ..........................250 lacteana, Bactra.....................................259 lacticolella, Blastobasis.................255, 281 lacustrata, Dipleurina... .....262 laetana, Ancyclis......................................63 laetus, Oxyptilus ..................................3, 12 laevigella, Monopis. ............. ..................2A6 l-album, Mythimna.. ......... ................IH, 162 lambdella, Batia.. ................. ..................252 lanella. Tinea .................................2A2, 246 lanestris, Eriogaster ..............................277 langiella, Mompha.. ............. ..................256 lappella, Metzneria.... ............. .........62, 253 laricana, Spilonota .....260 larseniella, Syncopacma.. ................... ...255 lateritia, Apamea 164 lathonia, Issoria... 13 leautieri, Lithophane... .................... .19, 282 leucatella, Recurvaria.. ............254 leucogaster, Ochropleura ........A, 18, 160 leucographella, Phyllonorycter ............. 28 1 leucomelas, Aedia .........................67 leucotreta, Thaumatotibia... .................. .2, 1 Ubatrix, Scoliopteryx.. .............. ......\\6, 111 licarsisalis, Herpetogramma .lAl , 152, 264 Uchenaria, Cleorodes... .............. .............. 14 lichenella, Da/i/ica.... ............................. 246 lienigialis, Pyralis.. .............................. ..153 lienigianus, Ovendenia ..........................266 ligustri, Craniophora... .................. .....92-9A ligustri, Sphinx.. .......................... ...........219 limbata, Evergestis... ....... ...........H, 151, 263 Umbella, Scythris ...................................256 lineana, Apotomis ..................................258 linearia, Cyclophora.. ............. .......229, 282 lineata, Siona ......................................... 126 Uneatella, Anarsia.... ........................ ..1 , 255 lineola, Eudonia. ................. .............A5, 262 lineola, Thymelicus.. ............................ ....59 linetella, Chrysocrambus....................... 179 linneella, Chrysoclista.. ....................... ..256 lipsiana, Acleris ............................... A5, 258 littoralis, Mythimna ............................... ..A6 littoralis, Spodoptera. ...................... ....2, 20 littorella, Metzneria ...............................253 litura, AgrocAola....... ............................ .278 livornica, iifyles ............ 1=2, 4, 16, 145, 157 lixella, Coleophora ................................250 lobarzewskii, Grapholita .......................261 lobelia, Luquetia.. ............................ ......252 xii loganella, logiana, Acleris. ........................ .44, 62, 258 longana, Cnephasia.........................62, 258 loreyi, Mythimna.. ...... ..4, 19, 146, 147, 162 lucella, ........ ........................ .249 lucens, Amphipoea.... ..................... ..20, 164 lucida, Acontia.. ........ .......3, 4, 21, 146, 165 luctuosa, Tyta... ............... ..22, 127-129, 167 luna, Actias ..........................................2, 13 lunaedactyla, Marasmarcha... ........ .......266 lunaris, Batia .........................................252 lunula, Calophasia. ............... ..3^, 143, 163, 274-276, 287 lunulana, Grapholita .............................261 lunuiaria, Selenia. ...................... ......14, 156 lutulentella, Monochroa.........................254 lychnitis, Shargacucullia .................. 97- 1 02 machaon, Papilio... ...... .....I, 3, 12, 37, 154, 179, 180 magdalenae, Stigmella. ..................... .....245 malinellus, Yponomeuta.. .................. .....249 malvae, Pyrgus............. ....................... ...12^ malvella, Pexicopia.. ....................... .......255 manniana, Phalonidia.... ........ ............... .257 margaritata, Campaea........ ................ ...2%2 margariteila, Catoptria...... 151 maritima, Bucculatrix............................247 masculella, Incurvaria...................22^, 229 mayrella, Coleophora ............................250 medicaginis, Cydia ................................ 150 megera, Lasiommata..........................5l, 53 megerella, Elachista ..............................252 melloneila, Galleria.......... ....... ..............264 messaniella, Phyllonorycter ..................247 messingiella, Eidophasia ....................... 250 metaxelia, Nematopogon .......................245 micalis, Tebenna ........................................6 millieridactyla, Stenoptilia ....................282 minimella, Nemophora ..........................245 miniosa, Orthosia ............................18, 162 ministrana, Eulia ...................................257 mitt-erbacheriana, AncycUs ...................... 63 molesta, Grapholita ..................... ......7 , 150 molliculana, Cochylis ................62, 68, 257 monacha, Lymantria... ............. ......279, 282 monachella, Monopis. ................ ...... ...... 148 monodactyla, Emmelina ........................266 montanata, Xanthorhoe ...........................63 morosa, LampmwM. ........................... ....245 moujfetella, Af/irips.... ............................ 254 mucronellus, Donacaula.. ....... ...8, 151, 262 muscerda, Pelosia............................l7 , 159 myrtillana, Ancylis. ............................. ...259 myrtillana, Rhopobota.. ...... ................ ...260 myrtillella, Stigmella.. ........... .................244 nana, Cochylis .......................................257 nanella, Recurvaria ...............................254 napi, Pieris. ............................. .................53 nebulella, Homoeosoma ........................265 nerii, Daphnis ..........................................15 nervosa, Agonopterix.... ........ ............... ..253 ni, Trichoplusia. ....... ......I, 21, 38, 146, 166 nicellii, Phyllonorycter ..........................248 nickerlii, Luperina .................................278 niditana, Strophedra...... ....... ...........62, 260 nigra ab. of ligustri, Craniophora......92-94 nigra, Gelechia ......................................254 nigrata, Pyramta.. ........................... ......263 nigricans, .............................. ....278 nigricomella, Bucculatrix ...................... 247 nigricostana, Endotkenia. ...................... 259 nigropunctata, Scapula....... .......14, 37, 155 nitentella, Scrobipalpa...........................255 noctuella, Nomophilal, 4, 24, 59, 145, 168, 169, 238, 263 notana, Acleris................ ....................... 258 nubiferana, Hedya .................................258 nubigera, Heliothis .....2, 3, 20, 38, 57, 106, 146, 165 nubilalis, Ostrinia.... ....... ...8, 152, 180, 263 nupta, Catocfllfl............................... ....... 280 nymphaeata, Elophila... ........................ .262 obductella, Pempelia .............................264 obfuscatus, Gwop/ios.. ............................ 123 obliquella, Elachista.. ............................252 oblitella, Ancyclosis ........ .........ll, 154, 265 obscurana, Pammene.............. ....... ........260 obscurepunctella, Perittia. ..................... 25 1 obsitalis, Hypena ..............22, 116-118, 167 obsoleta ab. of icteritia, Xanthia ..........121 obsoletella, Scrobipalpa ........................255 obstipata, Orthonama. ............ .28, 145, 172 obumbratana, Eucosma.........................260 occulta, Eurois ...............................161, 282 ocellaris, Xanthia.. ....................... ....20, 164 ocellatella, Scrobipalpa. .................. ......255 ocellea, Euchromius......!, 2, 4, 7, 145, 146, 150, 262 ochraceella, Mompha ............................256 ochrata, Maea. ........................... ....... .....155 ochrearia, Semmspilates........................206 ohridella, Cameraria ..................... 242, 248 oleastrella, Zellaria .......................242, 249 olivacea ab. of ligustri, Craniophora 92-94 olivalis, Udea.. ............................ ...........263 ononaria, Aplasta .................................... 13 operculella, Phthorimaea ......................255 orbona, Noctua............................ ...203-211 orbonalis, Leiicmocles.... ...................... ..264 orichalcea, Cosmopterix........ ................ 256 orichalcea, Thysanoplusia ................... 3 , 22 orobana, Grapholita..............................26\ orobi, Leucoptera...................................250 osseatella, Euzophera..........................!, 11 ostrina, EnMeiwma.. .............................. ...20 pactolia, Dryadaula. ...... ..................... ...246 xiii pallida, Eudonia 262 pallidactyla, Platyptilia ...266 pallidata, Evergestis 263, 266 pallustris, Athetis... 129-130 paludella, Calamotropha 28 1 palustrella, Monochroa 253 pamphilus, Coenonympha .51, 53, 54 papealis, Sitochroa... 8, 151 paradoxa, Stigmella 244 parasite 1 1 a, Euzophera 265 parenthesella, Ypsolopha 249 parva, Euhlemma....... 20, 165 panndactylus, Oxyptilus 265 pastinum, Lygephila 280 paupella, Ptocheuusa 254 pectinea, Incurvaria 228-229, 245 pedella, Stathmopoda ..255 peltigera, Heliothis ..35-36, 38, 145, 178 peregrina. Prays ...242, 249 perlella, Chilo 262 perlepidella, Digitivalva 250 perlucidalis, Phlyctaenia ...263, 281 petiverella, Diclirorampha 26 1 phaskmipemiella, Calyhites. 247 phlaeas, Lycaena 51, 53 phragmitella, Chilo.... 262 phycidella, Blastohasis 2, 7 piercei, Aethes ..257 piercella, Nitidinea 62 pigra, Clostera 286 pinguis, Euzophera 265, 280 pini, Dendrolimus 2, 3, 13, 37, 147, 155, 180, 231-233 pinicolana, Rhyacionia ...260 pinicolella, Batrachedra 256 platani, Phyllonorycter 247 platani, Stigmella 28 1 platanoidella, Phyllonorycter ..248, 281 plebejana, Crocidosema ........150, 259, 281 plexippus, Danaus 13, 155, 179 plumbana, Diclirorampha 261 plumigeralis, Pechipogo 3, 22, 274 podaliriiis, Iphiclides .154, 180 podana, A rchips 257 politella, Bryotropha.. 254 polychloros, Aglais 13, 37 polychromella, Syncopacma 255 polygonalis, Uresiphita .....8, 151, 179 polygrammata, Costaconvexa 180 polyxena, Zerynthia 2, 12 pomerana, Elachista 252 pomonella, Cydia .261 populetorum, Caloptilia.. 247 porcellus, Deilephila..... ..108 porphyrana, Eudemis .259 porrectella, Plutella .250 postvittana, Epiphyas ...251 , 281 potentillae, Coleophora 250 potentillella, Scythris ...71, 256 poterii, Stigmella 244 praeangusta, Batrachedra .....256 pratella, Crambus .....151 pretiosa, Stigmella 244 proboscidalis, Hypena .......282 processionea, Thaumetopaea 146, 158 pronuba, Noctua 18, 160, 267-273, 279 pronubana, Cacoecimorpha ........281 propinqiiella, Agonopterix 253 propinquella, Mompha 256 proximella, Carpatolechia 254 prunalis, Udea 263 pulchella, Utetheisa 4, 17, 238 pulchrimella, Cosmopterix 149, 242 pulveralis, Psammotis 3, 9, 152 puppillaria, Cyclophora 13, 155 purdeyi, Clavigesta 260 purpurea, Agonopterix 253 purpurina, Eublemma 1 46, 1 65 puta, Agrotis 280 pygniaeola. Edema .......17, 159 pyralella, Scoparia 262 pyri, Saturnia. ..2, 13, 155 pyrrhulipennella, Coleophora 251 quadra, Lithosia .17, 59, 159, 180, 181 quadrillella, Ethmia 149 quadrimaculana, Endothenia 259 quadripuncta, Oegoconia 255 quadripunctaria, Euplagia 17, 159, 274 quercana, Carcina 252 quinqueguttella, Phyllonorycter 248 ramburialis, Diaserniopsis 1, 9, 152, 180, 266 ramulicola, Phyllocnistis 242, 248 rapae, Pieris .....53 raptricula, Cryphia 3, 20, 164 reaumurella, Adela 245 recurvalis, Hymenia 62, 264 recurvalis, Spoladea ....238 regificella, Elachista.. 64-65, 252 reliquana, Lobesia .....259 re mm i, Mesapamea ..233-234 reversalis, Uresiphita *......59-61,242, 263 rhainn i, Gonopteryx ..53 rhamniella, Sorhagenia .....256 rhododactyla, Cnaemidophorus 266 rhombana, Acleris 25 8 ribeata, Deileptenia ...280 ripae, Agrotis .......46 rivulana, Celypha 258 roborana, Epiblema. ...260 roboris, Phyllonorycter ...247 robustana, Bactra 259 rorrella, Yponorneuta 6, 149 rosaceana, Celypha ...........258 rostralis, Hypena......... ....1 16 rubigana, Aethes. .......257 XIV rubiginata, Scopula..................lA, 155, 209 rubiginea, Conistra................................ 163 rubricollis, Atolmis ......... rufana, Celypha .....................................258 ruficiliaria, Cyclophora............2, 3, 14, 37, 147, 155 rufipennella, rufocinerea, rupicola, Cochylidia ..............................257 mralis, F/ewroplja... .............................. 264 rusticata, 155, 279 sacchari, Opogona.... .......................... ...2, 6 sacraria, Rhodometra...............!, 4, 27, 59, 145, 147, 172 sagitella, Phyllonorycter........................2A^ salaciella, Opostega ...................... ........2A5 salicata, Nebula.. ............................... ....155 salicella, Hedya .....................................258 salicicolella, Phyllonorycter ................. 248 salicorniae, Coleophora ....................... .251 saligna, Phyllocnistis.............................24H salopiella, Eriocrania............................2AA samadensis, Scrobipalpa .......................255 sambucaria, Oumpteryx.. ...................... 2H2 samiatella, Stigmella........... ................ ...2AA sarcitrella, Endrosis. .......................... ....252 saucia, Peridroma.... ....... .................32, 175 saxicola, Phycitodes ..............................265 saxicolella, Coleophora..... ............... .....251 scabrella, Ypsolopha.. ....................... .....2A9 scalariella, Dialectica....................\A6, 149 schreberella, Phyllonorycter.................. 195 schumacherana, Olindia........................25K scirpi, Biselachista.... ....................... ......252 scopariella, Agonopterix. ................ .......253 scotinella, Gelechia .........................62, 254 scribaiella, Cosmopterix. ...................... .736 scrophulariae, Shargacucullia .........97=102 secalis, Mesapamea.... .............. ......233~23A selene, Actias ......................................... 155 selene, Boloria.......................................l30 semele, Hipparchia.... .................... ........2Q6 semicostella, Sophronia. ....... ...........6^, 255 semifascia, Caloptilia ........................... .2A1 semirubella, Onocera ....................154, 264 semitestacella, Argyresthia....................2A9 senecionana, Clepsis.......... .................... 251 senticetella, Gelechia............................. 25A septembreila, Ectodemia. ...... ................ .244 sequella, Ypsolopha ...............................249 sericealis, Rivula..............................22, 167 sericopeza, Ectodemia... .................... ....244 signaria, Macaria ............................14, 156 silvella, Cra/wtej. ...................................... 8 similella, Elegia.....................................265 similis, Bryotropha.................. ........ .......25A simplex, Anatrachyntis... ...... ................... .3^ simulans, Rhyacia..................................\6Q singula, Neofriseria .................................62 sodaliana, Phtkeochroa.........................251 sordidana, Epinotia ...............................259 sordidatella, Depresaria........................253 sororcula, Eilema....... .................. ..\59, 279 sparrmannella, Eriocrania .................... 244 spartiella, Anarsia .................................255 spartifoliella, Leucoptera ......................250 speciosa, Stigmella ........................244, 281 spectrana, Clepsis.................................. 236 spiniana, Pammene. ............ ................... 260 splendens, Lacanobia .........2, 3, 18, 38, 57, 146, 162 sponsa, Catocala... .............. ...146, 167, 180 squamosella, Coleophora ......................202 stachydalis, Phylctaenia ..........................37 stagnata, Nymphula. .............................. 263 steinkellneriana, Semioscopis.. .............. 252 stellatarum, Macroglossum \ , 30-31, 108, 147, 168, 173 sternipennella, Coleophora .............. .....25\ sticticalis, Loxostege..................^, 151,263 striatella, Isophrictis.. ........ ................ ....253 striatipennella, Coleophora ................... 25 1 strigilata, Pechipogo................ .............. 211 strigulatella, Phyllonorycter.. ...... ..24^, 281 striolella, MAYmea........ ........................ 246 sturnipennella, Mompha.. ....... .......256, 281 suaedella, Scrobipalpa.. ..................... ....254 suavella, Trac^cera. ............... 11, 154, 264 subaquilea, Denisia ...............................252 subbistrigella, Mompha.......... ....... ........256 suberivora, Stigmella....... ................. .....244 subfusca, Scoparia.. ...................... .........262 subocellea, Elachista....... .............. ........252 subpropinquella, Agonopterix..................! 1 subpurpurella, Eriocrania .....................243 subsericeata, Idaea. ............................ ...220 sujfusa ab. of icteritia, Xanthia .............121 sulphurella, Esperia. ........................... ...252 suspectana, Pammene..... .......................260 svendseni f. of hyperici, Chloantha....... 143 sylvella, Ypsolopha.................................249 sylvestraria, Idaea .................................220 sylvestrella, Dioryctria.............\l, 154, 265 sylvestris, Thymelicus ..............................50 taenialis, Schrankia ............................... 193 taeniipennella, Coleophora ...................251 tamesis, Coleophora......... .....................251 temerata, Lomographa .......................... 156 tenebrella, Monochroa.. ......................... 253 tenebrosana, GrapAo/ito.......... .............. 261 tengstromi, Elachista.............. ....64-65, 252 tentaculella, Ancyclolomia. ................2,3,8 terebrella, Assara. ................ ............ 1 1, 265 testalis, Hodebertis ........................242, 264 tetragonella, Monochroa .......................253 tetralunaria, Selenia ..............................220 XV therinella, Coleophora...........................25l thoracella, Bucculatrix . ................ .19^, 247 thrasonella, GlypMpterix...............24-^, 266 tiliae, Mimas .......................................... 2H0 tiliae, Stigmella.. ........................ ......62, 245 tineana, A«cy/w.. .................... ........242, 259 tithonus, Pyronia.......... ........................... .52 tityus, Hemaris.......... ............................. 271 togata, Xanthia ...................................... 121 torquatella, Atemelia..............................249 transversata, Eupsilia.. ............. .............\\6 treitschkiella, Antispila ..........................245 tricolor, Coleophora ..209 trifasciata, A rgyresth ia 249 ,281 trifolii, Coleophora....... ................... ......259 trifolii, Discestra. 146, 161 trifolii, Lasiocampa..... ..............278 trigeminella, Coleophora....................... 259 trigonella, Epinotia.... ............................ 259 frimaculana, Epiblema ..........................269 trimaculella, Stigmella.. .................... .....244 trinotella, Tinea...................................... 247 tripoliana, Eucosma. .............................. 269 tristrigella, Phyllonorycter .................... 195 tritophus, Notodofita. ............................ .15^ trochilella, Coleophora. ................... ......25 1 tubulosa, Taleporia ......................246 tumidana, Conobathra ....11, 146, 153 turbidana, Apotomis .....259 turbidella, Ectoedemia... ......266 turca, Mythimna ............................. 133-142 turionella, Pseudococcyx. .................. ....269 uddmanniana, Epiblema........................ 269 ulceratalis, Cornifrons ........56-58, 237-238 uliginosalis, Udea. ....................242, 263 uliginosellus, Chilo.. ......................... .....262 ulmella, Bucculatrix ............... \96-\98, 247 ulmifoliae, Bucculatrix 195-201, 242, 247, 288 ulmivora, Stigmella................................ 195 ultimaria, Eupithecia ...................... .14, 156 ultimella, Depressaria ...........................252 umbrana, Ac/em....... ............................. 258 undalis, Hellula... ............................. ......262 unguicella, Ancylis.... ....... ................... ...259 unicolorella, Eulamprotes...................... 252 unipuncta, Mythimna.... ............. ..4, 33, 176 unipunctella, Phyllocnistis. .................... 248 upupana, Ancylis. ................................... 259 urella, Ochsenheimeria..........................249 urticae, Ag!ais................5l, 53, 54, 55, 116 ustulana, Endothenia.... .................... .....259 vancouverana, Dichrorampha ............... 26 1 variatella, Nemapogon ..........................246 velocella, Aroga.. .................................. .254 venata, Ochlodes........... .............. .51, 53, 54 verbascalis, Anania.... ........................... .262 verbasci, Shargacucullia .................. 97- 1 02 verellus, Catoptria ...........................68, 262 versurella, Coleophora. ................. ........25 1 vestianella, Coleophora................... 62, 251 vetusta, Xylena.... 19, 163 vibicella, Coleophora............................. 1 1 1 viretata, Acfli'w.. ..................................... 282 virgata ab. oficteritia, Xanthia ............. 121 virgata, Phibalapteryx ...........................211 virginiensis, Vanessa.. .............. ....4, 13, 154 viridis, Antichloris ................................... 17 viriplaca, Heliothis ....................... .165, 209 viscariella, Caryocolum.........................255 viscerella, Stigmella...............................\95 vitellina, Mythimna....................... ...22, 176 vitrata, Maruca. ................... ..2, 9, 147, 152 vitrealis, Palpita... ...... ....I, 10, 59, 152, 264 vittella, Earias.... ................................. .2, 21 wauaria, Macaria ..................................278 weirana, Strophedra ..............................269 wilkella, Eulamprotes ............................252 williana, A^r/ie^..... ................................. 257 wolffiella, Nemapogon. .......................... 246 xanthographa, Xesf/fl......... .................... 206 xylostella, Plutella ...................22, 168, 250 yeatiana, A^onop/enx. ........................... 253 zinckenella, Etiella....... 265 zonaria, Lycia 278 COLEOPTERA Diaperis boleti...... .................... ..14-15, 108 Harmonia axyridis ...................................82 Laemophloeus monilis .............................94 Malachius aeneus ....................................46 Platycis minutus.... ................................... 45 Sinodendron cy/m 1 iff 1-May 16-May 31-May 15-Jun 30-Jun 15-Jul 30-Jul 14-Aug 29-Aug 13-Sep 13-Oct 28-Oct 12-Nov 27-Nov Fig. 10. Occurrence times of Mythimna loreyi during 2003 (dated records). 2240 Lithophane leautieri hesperica (Hours.) Blair’s Shoulder-knot [R][V/I] ISLE OF MAN [71] Dhoon Maughold, 29.9 - 28.10 (17) (per GDC). Probably breeding on the island. Also now likely to be breeding in Ireland where this species was recorded from two locations in H20 that produced the first Irish records in 2002 (per IR). 2241 Xylena vetmta (Hb.) Red Sword-grass [R][I][V] S. SOMERSET [5] Nr. Exford, 23.4 (A. Middleton per SN). DORSET [9] Puddletown, 29.4 (HWH); Shapwick, 24.3 (PAD); Slepe Farm, 25.3, 2.4, 3.4 (D. Cooper); Woolland, 12.4 (P. Benham per PAD). 2242 Xylena exsoleta (L.) Sword-grass [R][I][V] E. SUFFOLK [25] Reydon, 20.9 (AC per AWP). 2251 Trigonophora flammea (Esp.) Flame Brocade [I][FR] S. HAMPSHIRE [11] Hengistbury Head, 10.10 (Ml). E. KENT [15] Pegwell, 3.10 (FS). 2261 Conistra erythrocephala (D. & S.) Red-headed Chestnut [I][FR] S. SOMERSET [5] Norton Sub Hamdon, 25.11 (IM). E. SUSSEX [14] Peacehaven, 5.11 (CRP). N. ESSEX [19] Dovercourt, 8.11, first county record (CG). 20 ENTOMOLOGIST'S RECORD, VOL. 119 25.1.2007 2275 Xanthia gilvago (D. & S.) Dusky-lemon Sallow [R][V/I] W. CORNWALL [1] The Lizard, 13.10, 21.10 (SN, APR); lOS: St Mary’s, Longstone, 23.10, (Scott, 2004a). The first county records. 2276 Xanthia ocellaris (Borkh.) Pale-lemon Sallow [R][I][V] S. HAMPSHIRE [11] Southsea, 3.10 (IRT), first county record. W. SUSSEX [13] Kingsham, 13.10 (SJP per CRP); Walberton, 7.10, 10.10 (JTR per CRP). E. KENT [15] Dungeness, 22.9 (KR per SPC); Ramsgate, 8.10 (FS). 2290 Simyra albovenosa (Goeze) Reed Dagger [R][V/I] W. SUSSEX [14] Kingsham, 14.7, 16.7 (Patton, 2004). S.E. YORKSHIRE [61] Kilnsea, 15.7, 16.7; Spurn, 16.7, 7.8 (BRS). 2292 Cryphia algae (Fabr.) Tree-lichen Beauty [I][MC] Total no. reported: 36 DORSET [9] Durlston, 7.8 (JMc), 8.8 (SN); Portland Bird Observatory, 1.8 (MC). ISLE OF WIGHT [10] Bonchurch, 10.8, 11.8 (JH); Ventnor, 15.8, 17.8, 18.8 (Knill-Jones, 2004). S. HAMPSHIRE [11] Hayling Island, 4.8, 7.8 (Phillips, 2004). W. SUSSEX [13] Walberton, 1.8, 4.8 (JTR per CRP). E. SUSSEX [14] Hastings, 15.7 (NMH per CRP). E. KENT [15] Greatstone, 16.7, 7.8 (BB); Kingsgate, 1.8, 4.8, 6.8 (FS); Littlestone, 21.7 (KR); New Romney, 5.8 (KR); Pegwell, 8.8 (FS); Ramsgate, 24.7 (Solly, 2004). W. KENT [16] Dartford, 28.7, 10.8 (West, 2004); Woolwich, 6.8 (R. Clark). N. ESSEX [19] Kirby-le-Soken, 25.7 (PB); Little Oakley, 22.7 (GS), first county records. MIDDLESEX [21] Regents Park, London, 8.7, 20.7, 12.8 (2) (THE). E. SUFFOLK [25] Landguard Bird Observatory, 10.7, 15.7, 22.7, 2.8, 5-6.8 (Odin, 2004), first county records. 2294 Cryphia raptricula (D. & S.) Marbled Grey [I] E. KENT [15] Greatstone, 10.8 (BB). E. SUFFOLK [25] Landguard Bird Observatory, 20.7, first county record (Odin, 2004). 2304 Trachea atriplicis (L.) Orache Moth [I][FR] S. DEVON [3] Dawlish, 2.7 (PF, in Collins, 2004). DORSET [9] Portland Bird Observatory, 19.7 (Cade, 2004); Upwey, 31.7 (PH). ISLE OF WIGHT [10] Bonchurch, 4.7 (JH). W. SUSSEX [13] Middleton-on-Sea, 4.7, first county record (O. Laughame per CRP). 2097a Actinotia hyperici (D. & S.) Pale-shouldered Cloud [I] E. SUFFOLK [25] Landguard Bird Observatory, 6.5, 3.6, first county records (Odin, 2004). 2349 Chortodes fluxa (Hb.) Mere Wainscot [R][V/I] S.E. YORKSHIRE [61] Kilnsea, 6.8 (BRS). 2357 Amphipoea lucens (Frey.) Large Ear [R][I] N. ESSEX [19] Kirby-le-Soken, 7.8, third county record (PB, BG). 2386 Spodoptera littoralis (Boisd.) Mediterranean Brocade [In][I] SURREY [17] Carshalton, 16.6 (D.A. Coleman, in Collins, 2004). 2387a Platyperigea kadenii (Frey.) Clancy’s Rustic [I] S. HAMPSHIRE [11] Southsea, 11.7, first county record (JRL). W. SUSSEX [13] Walberton, 27.6, first county record (JTR per CRP). E. KENT [15] Greatstone, 4.7, 18.9 (BB); Lydd, 21.9, 8.10 (CT per SPC). 2392a Proxenus hospes (Frey.) Porter’s Rustic [I] W. CORNWALL [1] lOS: St Agnes, 13.9, 16.9 (MEH); lOS: St Mary’s, Longstone, 17.9, 20.9, 26.9 (MAS). DORSET [9] Portland Bird Observatory, 13.8, first county record (MC). 2404 Heliothis nubigera (H.-S.) Eastern Bordered Straw [I] W. CORNWALL [1] lOS: St Mary’s, Longstone, 17.6, 25.6, first county records (MAS). DORSET [9] West Bexiimton, 25.6 (RE). ISLE OF WIGHT [10] Coastguard Cottages, Needles, 23.7, first county record (DH , M.C. Harvey). S. ESSEX [18] Maldon, 8.6, first county record (R. Neave, S. Wood per BG). 2407 Eublemma ostrina (Hb.) Purple Marbled [I] W. CORNWALL [1] Maenporth, 5.11 (GD). DORSET [9] Durlston, 26.6 (2) (PAD, SN); Portland Bird Observatory, 24.8 (Cade, 2004). 2408 Eublemma parva (Hb.) Small Marbled [I] DORSET [9] Preston, 30.6 (RL); West Bexington, 25.6, 24.8 (RE). N. HAMPSHIRE [12] Selborne, 10.7 (AEA). S. LANCASHIRE [59] Pennington, 13.7 (PPper SMP). 2413 Deltote bankiana (Fab.) Silver Barred [R][ W] E. KENT [15] Dumpton, 19.6 (Solly, 2004); Kingsdown, 22.6 (FS); Littlestone, 30.6 (KR). W. KENT [16] Grain, 26.6 (AGJB) (not 26.4 as given in Collins, 2004). N. ESSEX [19] Copperas Wood, near Ramsey, 5.7 (P. Smith per BG); Dovercourt, 3.7 (CG); Frinton-on-Sea, 2.7 (B. Lock per BG). 2003 IMMIGRATION REVIEW 21 2415 Acontia lucida (Hufn.) Pale Shoulder [II W. CORNWALL [1] lOS: St Agnes, 14.7 (MEH). W. SUSSEX [13] Kingsham, 6.8 (SJP per CRP). E. KENT [15] Lydd-OE-Sea, 21.9 (RC per SPC). 2418 Earias clorana (L.) Cream-bordered Green Pea [R][FV] W. CORNWALL [1] lOS: St Agnes, 17.7 (Hicks, 2004). 2420a Earias vittella (Fabr.) [In?] DORSET [9] DurlstoE, 16.6, to light. A pest species of cotton & okra pods, only previously recorded in Britain as an intercept (Nash, 2003). 2423 Nycteola miatica (KruL) Eastern Nycteoiine [I] E. KENT [15] Dungeness, 2.7 (DW, SPC, det. MRH). 2428 Chrysodeixis chakites (Esp.) Golden Twin-spot [I] [In] Total no. immigrants reported: 8 W. CORNWALL [1] Church Cove, The Lizard, 25.9 (Tunmore, 2004); lOS: St Agnes, 1.10, new to the Scillies (Hicks, 2004). S. ESSEX [18] Maldon, 7.9 (R. Neave per BG). E. SUFFOLK [25] Dunwich, 5.9 (JBH, AJM); Landguard Bird Observatory, 19.8, 2.10 [second date published in error as 19.9 in Odin, 2004] (NO). W. LANCASHIRE [60] Heysham, 5.7 (J. Holding per SMP), first county record. S.E. YORKSHIRE [61] Filey, 3.10 (anon.). E. CORNWALL [2] A colony established within one of the biomes at the Eden Project, Bodelva, with a number of larvae present on 26.3 & 30.5 (J.L. Gregory), and regular records of adults and larvae subsequently (J.L. Gregory, pers. comm.). 2432 Trichoplmia mi (Hb.) Nl Moth [I] Total no. reported: 58 W. CORNWALL [1] Church Cove, The Lizard, 6.8 (Tunmore, 2004); lOS: St Agnes, 14.7, 6.8 (Hicks, 2004), 14.10 (Davison, 2004); lOS: St Mary’s, Longstone, 26.6, 4.7 (Scott, 2004a). N. DEVON [4] Hartland Point, 22.6 (BPH, RFM), 6.9, by day (P. Bryant). S. SOMERSET [5] Staplegrove, 28.8 (JMc). N. SOMERSET [6] Buraham-on-Sea, 25.6 (2) (A. Slade). DORSET [9] Cheyne Wears, Portland, 4.7 (SPC); Durlston, 26.6 (PAD, SN), 19.8 (2) (DCGB), 22.8 (PAD); Freshwater Bay, Portland, 23.8 (JEC, J. Spence); Portland Bird Observatory, 26.6, 13.8 (2), 23.8 (2) (MC per PAD); Preston, 27.6 (MF); Studland, 2.9 (DCGB); Upwey, 25.8 (PH); West Bexington, 26.6, 7.8, 13.8, 15.8, 27.8, 1.9, 4.9 (RE per PAD); Wyke Regis, 7.8, 23.8 (DF). ISLE OF WIGHT [10] Bonchurch, 11.8 (JH); Freshwater, 26.6 (DBW); Totland, 8.7 (SAK-J). S. HAMPSHIRE [11] Beaulieu, 10.8 (B. Ivon- Jones per TN); Southsea, 8.8, 12.8 (JRL per TN). N. HAMPSHIRE [12] Nr. Andover, 9.8 (TN). W. SUSSEX [13] Kingsham, m 0 1-Jun ■I 16-Jun 1-Jul ie-Jul 31-Jul 15-Aug 30-Aug Fig. 11. Occurrence times of Trichoplusia ni during 2003 (dated records). rnmmmmmmm 29-Sep 14-Oct 22 ENTOMOLOGIST'S RECORD, VOL. 119 25.1.2007 14.7 (SJP per CRP); Lyminster, 14.8 (R.E. Pratt per CRP). E. SUSSEX [14] Winchelsea, 5.7 (JEC, J. Spence per CRP). E. KENT [15] Dymchurch, 18.8 (JO); Kingsgate, 23.6, 15.7 (FS); New Romney, 13.8 (KR). W. KENT [16] Halstead, 24.6 (J. East). S. ESSEX [18] Bradwell-on-Sea, 21.8 (Dewick, 2004). BERKSHIRE [22] Femham, 13.8 (SN). W. NORFOLK [28] Holme-next-the-Sea, 22.8 (P. Clarke per DH). GLAMORGAN [41] Roath, Cardiff, 3.9 (DRWG). CARMARTHENSHIRE [44] Pembry, 2.7, 24.8 (J. Baker). S. LANCASHIRE [59] Orrell, 21.8 (P. Alker per SMP). W. CORK [H3] Crookhaven, 14-19.9 (Allen & Mellon, 2004). WICKLOW [H20] Ashford, 10.9 (AT). 2433 Trysanoplusia orichalcea (Frey.) Slender Burnished Brass [I][In] W. CORNWALL [1] Church Cove, The Lizard, 18.11 (Tunmore, 2004); lOS: St Agnes, 7.8 (MEH), 12.10 (MEH per AD); [latter record incorrectly given as 23.10 in Hicks, 2004]. 2436 Macdunnoughia confusa (Steph.) Dewick’s Plusia [I][In] DORSET [9] Portland Bird Observatory, 28.6 (MC); Upwey, 9.9 (PH); Weymouth, 17.9 (PHS). S. HANTS [11] Catherington, 26.8 (RJM perTN); Lymington, 5.9 (Harmer, 2004); Southsea, 1.9 (IRT). E. KENT [15] Dungeness, 21.9 (DW). 2444 Autographa bractea (D. & S.) Gold Spangle [R][V/I] E. NORFOLK [27] Stiffkey, 5.8 (T. Crafer per DH). S.E. YORKSHIRE [61] Kilnsea, 26.7 (BRS); Spurn, 10.7 (BRS). 2451 Catocala fraxini (L.) Clifden Nonpareil [I][FR] W. CORNWALL [1] lOS: St Mary’s, Longstone, 11.9, new to the Scillies (Scott, 2004a). [There were also unconfirmed records from Southend [18] on 3.9 (R. Mullins per SN); and Maidenhead [22] on 14.9 (J. Hawksley per THE).] 2465 Tyta luctuosa (D. & S.) Four-spotted [R][W] E. KENT [15] New Romney, 17.7 (SPC). 2475 Parascotia fuliginaria (L.) Waved Black [R][W] E. KENT [15] New Romney, 26.6, 15.7 (SPC), 12.7, 22.7 (KR). 2474 Rivula sericealis (Scop.) Straw Dot [R][V/I] The following records may relate to immigrants. DORSET [9] Merley, 4-8.8 (411) (J. Hammick); Shapwick, 21.9 (46) (PAD); Woolland, 10.8 (60), 20.9 (16) (P. Benham). S.E. YORKSHIRE [61] Kilnsea, 22.6 (PAC), 26.7 (BRS); Spurn and Kilnsea, 3.8 - 12.8 (37) (BRS); Spurn, 21.9 (BRS). 2478 Hypena obsitalis (Hb.) Bloxworth Snout [R][V/I] Records outside the known breeding range, most likely to relate to internal vagrancy. W. CORNWALL [1] Church Cove, The Lizard, 10.10 (Tunmore, 2004); Gerrans, 27.7 (A. Kershaw per SN); Mylor Churchtown, November, found in shed (Cooke, 2004). DORSET [9] Easton, Portland, 5.9 (RL); Portland Bird Observatory, 9.8 (MC); West Bexington, 4.9 (Eden, 2004). ISLE OF WIGHT [10] Bonchurch, 8.8 (JH). 2488a Pechipogo plumigeralis (Hb.) Plumed fan-foot [I] E. KENT [15] Greatstone, 10.10 (BB); Kingsgate, 1.8 (FS). 2495 Trisateles emortualis (D. & S.) Olive Crescent [R][I] DORSET [9] Portland Bird Observatory, 15.7 (Cade, 2004). E. SUSSEX [14] Rye Harbour, 6.8 (B. Yates per CRP). ANNEX 2i SELECTED RECORDS OF COMMONER MIGRANT SPECIES IN 2003 Detailed statistics are not provided for the diurnal species listed in Annex 2 due to the generalised, non-specific nature of reports of these species from several key sites. Significant records, site totals and general comments have been given for these species, but it is to be hoped that numerical occurrence records and monthly totals will be more widely available in future seasons. For the same reason, the totals given in the tables for partially diurnal species such as Plutella xylostella and Autographa gamma refer to light-trap records only where records are detailed more systematically. It has also not been possible to allocate months of occurrence to all 2003 IMMIGRATION REVIEW 23 the records of nocturnal Annex 2 species reported. It is therefore generally the case that the total given for the number of reported records is greater than the sum of the monthly totals given within the tables. Whilst it is likely that the records included in the tables will not be comprehensive for the commoner species, the geographical and chronological occurrence patterns presented should reflect the overall picture for each species. Key to the symbols used within the distribution tables: SW South-west England (VC’s 1-4). CS Central southern England (coastal) (VC’s 5, 6, 9-11, 13). SE South-east England (coastal) (VC’s 14-16, 18, 19). EA East Anglia & Lincolnshire (VC’s 25-28, 53, 54). SI Southern England (inland) (VC’s 7, 8, 12, 17, 20-24, 29-34). W Wales (VC’s 3S, 41-52). CE Central England (inland) (VC’s 36-40, 53-58), NE North-east England (VC’s 61, 62, 66-68). NW North-west England & the Isle of Man (VC’s 59, 60, 63-65, 69-71). S Scotland (VC’s 72-112). I Ireland (VC’s H1-H40). YPONOMEUTIDAE 0464 Fiuteiia xyimteOa (L.) [R][I] Total no. reported (light-trap records only): 18447 Distribution of records: SW CS SE EA SI W CE NE NW S I 1181 7479 6537 1349 737 170 479 158 123 52 182 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec - 3 22 107 169 1398 2183 646 202 158 117 6 Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 274 (Hicks, 2003); lOS: St Mary’s, Longstone - 613 (Scott, 2004a). S. DEVON [3] Starcross - 118 (Rothamsted Trap) (AHD). DORSET [9] Portland Bird Observatory - 2494 (Cade, 2004); West Bexington - 348 (Eden, 2004). W. SUSSEX [13] Kingsham - 2914 (Patton, 2004). E. SUSSEX [14] Peacehaven - 251 (Pratt, 2004). E. KENT [15] Isle of Thanet - 4876 at three sites (FS); Kingsdown - 311 (Jarman, 2004). HERTFORDSHIRE [20] Hertford - 81 (AW per CWP). E. NORFOLK [27] Eccles-on-Sea - 342 (Bowman, 2004). N. NORTHUMBERLAND [68] Whitley Bay - 48 (per KR^). Ealiest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 25.3 (Scott, 2004a). DORSET [9] Portland Bird Observatory, 22.3 (Cade, 2004); V/est Bexington, 26.3 (Eden, 2004). ISLE OF WIGHT [10] Bonchurch, 26.3 (JH). W. SUSSEX [13] Kingsham, 26.3 (Patton, 2004). BUCKINGHAMSHIRE [24] Near Milton Keynes, 21.2, indoors (LH). GLAMORGAN [41] Gower, 27.3 (Gilmore, 2004). W. LANCASHIRE [60] Heysham, 27.3 (J. Holding per SMP). WICKLOW [H20] Ashford, 8.2, 25.2, 24.3 (AT). Latest dates: DORSET [9] Portland Bird Observatory, 23.12 (MC). E. KENT [15] Thanet, 1.12 (Solly, 2004). N. ESSEX [19] Dovercourt, 3.12 (CG). S. LANCASHIRE [59] Parr, 4.12 (R. Banks per SMP). DURHAM [66] Marske, 4.12 (D. Money per SN). Large single night counts: W. CORNWALL [1] lOS: St Mary’s, Longstone, 5.7 (84) (Scott, 2004a). DORSET [9] Portland Bird Observatory, 10.8 (249) (Cade, 2004). W. SUSSEX [13] Kingsham, 26.6 (178); 19.7 (343) (SJP); Pagham, 2.6 (150) (SN). E. KENT [15] Kingsgate, 19.7 (309) (FS). E. SUFFOLK [25] Landguard Bird Observatory, 3.6 (236) (Odin, 2004). E. NORFOLK [27] Eccles-on- Sea, 3.7 (73) (Bowman, 2004). Large diurna! counts: S.E. YORKSHIRE [61] Spurn, ‘hundreds’ for a few days in mid-July (BRS). 24 ENTOMOLOGIST'S RECORD, VOL. 119 254.2007 Most northerly records: N. EBUDES [104] Raasay, 31.5 (S. Bradley per PC). SHETLAND ISLANDS [112] general VC, ‘reasonable numbers’ from 13.6 (anon.); Eswick, 19.5 (6), 20.5 (12), 28.5 (4) (TR); Foula 19.7, ‘abundant’, 30.7 (2) (G. & D. Atherton); Unst, 3.6, several by day (anon.). PYRALIDAE 1395 Udeaferrugalis (Hb.) [I] Total no. reported: 14311 Distribution of records: sw cs SE EA SI W CE NE NW S I 6780 6179 878 72 92 125 26 6 16 1 138 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec - 1 - 7 72 373 566 4937 883 1827 1023 125 Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 833 (MEH, AD); lOS: St Mary’s, Longstone - 4406 (Scott, 2004a); The Lizard - 1388 at three sites (Tunmore, 2004). S. DEVON [3] Starcross - 78 (Rothamsted Trap) (AHD). DORSET [9] Bridport area - 563 at two sites (Parsons & Brereton, 2004); Portland Bird Observatory - 1211 (Cade, 2004); West Bexington - 1572 (Eden, 2004). ISLE OF WIGHT [10] Approximate Island total - 2000 (Knill-Jones, 2004); Totland - 556 (SAK-J). W. SUSSEX [13] Selsey - 283 at two sites (Patton, 2004). E. SUSSEX [14] Elms Farm, Icklesham - 100 (Hunter, 2004); Peacehaven - 121 (Pratt, 2004). E. KENT [15] Dungeness area - 320+ at seven sites (Clancy, 2004); Isle of Thanet - 162 at three sites (FS). S. ESSEX [18] Bradwell-on-Sea - 148 (Dewick, 2004). PEMBROKESHIRE [45] Skomer Island - 60 (Hayden, 2004). WEXFORD [H12] Tacumshin area, 22-24.8 (69) (Allen, 2004). Ealiest dates: W. CORNWALL [1] St Mary’s, Longstone, 26.2 (Scott, 2004a). Latest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 24.12 (Scott, 2004a). E. CORNWALL [2] Bodelva, 24.12 (2) (Gregory, 2004). DORSET [9] Walditch, 27.12 (MSP). ISLE OF WIGHT [10] Freshwater, 24.12 (SAK-J). Large single night counts: W. CORNWALL [1] lOS: St Agnes, 13.10 (55) (Davison, 2004); lOS: St Mary’s, Longstone, 4.11 (82), 18.12 (34) (MAS). DORSET [9] Portland Bird Observatory, 12.8 (87) (Cade, 2004). Most northerly records: S. LANCASHIRE [59] Skelmersdale, 4.12 (C. Darbyshire per SMP). W. LANCASHIRE [60] St. Annes, 14.6 (J. Steeden per SMP). S.E. YORKSHIRE [61] Kilnsea, 15.8 (PAC); Spurn 10.8, 20.8, 8.9 (2) (BRS). N. NORTHUMBERLAND [68] Nunnykirk, near Longhorsley, 7.9 (per Kr2). ISLE OF MAN [71] Ballaugh, 23.8 (2) (per GDC); Knocksharry, 19.8, 21.8, 26.8 (per GDC); South Barrule, 25.8 (per GDC). ROXBURGHSHIRE [80] Harestanes, near Jedburgh, 3.9 (JW et al). Selected inland records: SURREY [17] South Croydon, 13.7 (GAC); Weybridge, 10.8 (A.R. Mitchell per GAC). HERTFORDSHIRE [20] Astonbury Wood, 16.6 (CWP); Bishops Stortford, 16.8, 18.8, 21.8, 22.8, 9.11, 17.11 (JF, CWP); Hertford, 12.8, 23.8, 20.11 (AW per CWP); Ware, 9.11 (EG per CWP). MIDDLESEX [21] Regent’s Park, 12.8 (THF). BERKSHIRE [22] Dry Sandford, 12.7, 3.8, 10.8 (2), 22.8 (2), 5.9 (AK). HUNTINGDONSHIRE [31] Hilton, 4.11 (BD); Kimbolton, 18.9 (BD); St Ives, 25.8 (BD); Woodwalton Fen, 22.8 (2), 19.9 (BD); Yaxley, 23.8 (A. Frost per BD). LEICESTERSHIRE [55] Clipsham Quarry, 9.8 (APR); Great Easton, 26.8 (J.M. Harvey per APR); Loddington, undated, five during the year (RIS per APR); Markfield, 23.8 (AIM per APR); Pickworth, 16.8 (APR); Rutland Water, 23.8 (RIS per APR); Whetstone, 15.8, 17.8 (2) (MPS per APR). NOTTINGHAMSHIRE [56] South Muskham, 14.8 (DA, MK); Sutton-on-Trent, 20.11 (MK). CHESHIRE [58] Alsager, 7.9 (M. Dale per SF); Bramhall, 22.8 (A. Charlton per SF). ROXBURGHSHIRE [80] Harestanes, near Jedburgh, 3.9 (JW et al). 1398 Nomophila noctuella (D. & S.) [I] Total no. reported: 127799 Distribution of records: SW CS SE EA SI W CE NE NW S I 45110 59610 13082 2414 1829 259 315 962 1860 31 2227 2003 IMMIGRATION REVIEW 25 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec - - 6 10 90 1595 3232 15486 44822 4993 232 3 Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 13300+ (Hicks, 2004), 11-16.10 - 462 (Davison, 2004); lOS: St Mary’s, Longstone - 21876 (Scott, 2004a); The Lizard - 2043 at three sites (Tunmore, 2004). DORSET [9] Bridport area - 1453 at two sites (Parsons & Brereton, 2004); Portland Bird Observatory - 26566 (Cade, 2004); West Bexington - 7765 (Eden, 2004). ISLE OF WIGHT [10] Approximate Island total - 10000 (Knill-Jones, 2004); Totland - 3700 (SAK-J). W. SUSSEX [13] Kingsham - 5256 (Patton, 2004). E. SUSSEX [14] Peacehaven - 2852 (Pratt, 2004); Elms Farm, Icklesham - 2047 (Hunter, 2004). E. KENT [15] Dungeness area - 3557+ at three sites (per SPC); Isle of Thanet- 2960 at three sites (FS). S. ESSEX [18] Bradwell-on-Sea - 1116 (Dewick, 2004). E. SUFFOLK [25] Landguard Bird Observatory - 1220 (Odin, 2004). E. NORFOLK [27] Eccles-on- Sea - 468 (Bowman, 2004). S.E. YORKSHIRE [61] Spurn area - 922 at three sites (BRS, PAC). WICKLOW [H20] Ashford - 928 (AT). W. CORK [H3] Crookhaven, 14-19.9 (901) (Allen & Mellon, 2004). Ealiest dates; W. CORNWALL [1] lOS: St Agnes, 5.4 (Hicks, 2004). E. CORNWALL [2] Looe, 26.3 (TS). DORSET [9] Portland Bird Observatory, 25.3 (Cade, 2004); West Bexington, 28.3 (Eden, 2004). W. SUSSEX [13] Kingsham, 28.3 (Patton, 2004). Latest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 30.11 (Scott, 2004a). N. WILTSHIRE [7] Highworth, 3.12 (SN). S. ESSEX [18] Bradwell-on-Sea, 4.12 (Dewick, 2004). WICKLOW [H20] Ashford, 24.12 (AT). Large single night counts: W. CORNWALL [1] lOS: St Agnes, 25.9 (c.4000) (Hicks, 2004), 13.10 (176) (Davison, 2004); lOS: St Mary’s, Longstone, 16.6 (198), 5.8 (232), 17.9 (4600) (MAS). DORSET [9] Portland Bird Observatory, 5.9 (5500) (Cade, 2004). S. HAMPSHIRE [11] Portchester, 7.8 (150) (IS). W. SUSSEX [13] Kingsham, 6.8 (259) (SJP). E. SUSSEX [14] Elms Farm, Icklesham, 12.8 (232), 17.9 (136) (Hunter, 2004). E. KENT [15] Dungeness area, 21.9 (659, at three sites) (per SPC); Kingsgate, 2.10 (147) (FS). S. ESSEX [18] Bradwell-on-Sea, 5.9 (115) (Dewick, 2004). E. SUFFOLK [25] Landguard Bird Observatory, 2.10 (343) (Odin, 2004). ISLE OF MAN [71] Dhoon Maughold, 14.9 (1000+) (per GDC). W. CORK [H3] Cape Clear Island, 13.10 (68) (per KB). WICKLOW [H20] Ashford, 10.9 (89) (AT). Large diurnal counts: W. CORNWALL [1] lOS: St Mary’s, Longstone, 9.5 - 30.11 (6834) (Scott, 2004a). Most northerly records: N. EBUDES [104] Raasay, 31.5 (S. Bradley per PC). SHETLAND ISLANDS [112] Eswick, 19-29.5 (11), 16.8 (TR); Foula, 19.7 (G. & D. Atherton); Ocraquoy, 7.9 (anon.). Selected inland records: HERTFORDSHIRE [20] 203 adults recorded across the county, 11.6 - 19.11 (per CWP). MIDDLESEX [21] Regent’s Park, 12.8 (75) (THF). BERKSHIRE [22] Dry Sandford, 13.6, recorded frequently thereafter (AK). CAMBRIDGESHIRE [29] Wicken, recorded commonly through September (DEW). HUNTINGDONSHIRE [31] 65 adults recorded across the county, 13.6 - 14.10 (per BD). LEICESTERSHIRE [55] 225+ adults recorded across the county, 8.7 - 19.10 (per APR). NOTTINGHAMSHIRE [56] Girton, 8.8 (DA); South Muskham, 6.8, 14.8, 17.9, 18.9, 4.10 (DA, MK); Sutton-on-Trent, 20.7, 5.8 (3), 7.8, 12.8, 22.9 (MK). CHESHIRE [58] Alsager, 24.8 - 3.10 (24) (M. Dale per SF); Bramhall, 14-19.9 (4) (A. Charlton per SF); Gawsworth, 20.9 (SHH); Higher Poynton, 17.8 (2) (SHH); Romiley, 10-23.8 (4), 11.10 (SF). ROXBURGHSHIRE [80] Allan Water, near Hawick, 14.5, 14.8 (JW); Bonavista, near Galashiels, 15.9 (JW); Caverton, near Kelso, 18.9, 19.9 (2) (T. Alampo per JW). Offshore record; A single moth at rest on a fishing boat c.5 miles south of Brighton [14], 3.9, at c.lO a.m. (A. Batten per CRP). PIERIDAE 1545 Colias crocem (Geoff.) Clouded Yellow [I][MC] Selected annual totals: W. CORNWALL [1] lOS: St Mary’s - 178 (Scott, 2004a). S. HAMPSHIRE [11] Gosport - 391 (D. Tinling). E. SUSSEX [14] Elms Farm, Icklesham - 79 (IDH per CRP). S. ESSEX [18] Bradwell-on-Sea - 40 (Dewick, 2004). PEMBROKESHIRE [45] Skomer Island - 28 (Hayden, 2004). W. CORK [H3] Dursey Island - 64+ (Scott, 2004b). Non-specific comments: W. CORNWALL [1] lOS: St Agnes, two seen in late June, and a small influx in September and into October (Hicks, 2004); The Lizard, small numbers seen regularly, particularly during the autumn (Tunmore, 2004). DORSET [9] Portland, 2.8 - 27.11, almost daily (Cade, 2004). ISLE OF WIGHT [10] Bonchurch, 3.8, a number seen coming in off the sea (JH). S.E. YORKSHIRE 26 ENTOMOLOGIST’S RECORD, VOL. 119 25.i.2007 [61] Spurn, 27.7 - 9.8 (1-3 most days), 9.9, 17.9, 1.10, 2.10 (Spence, 2003). Earliest dates: W. CORNWALL [1] near St Austell, 3.4, 4.4 (per RL). S. DEVON [3] Weston Coombe, 5.4 (R.M. Hill). ISLE OF WIGHT [10] First week of April (several) (Knill-Jones, 2004). Late.st dates: E. CORNWALL [2] Seaton, 4.12 (3) (L. Truscott). DORSET [9] Portland, 27.11 (Cade, 2004). ISLE OF WIGHT [10] Ventnor, 27.12 (A. Butler per SAK-J); Wheelers Bay, 27.11 (Knill-Jones, 2004). S. HAMPSHIRE [11] Gosport, 26.11, 27.11 (3), 28.11 (2) (D. Tinling). Large counts: DORSET [9] Portland, October (20 on several dates) (Cade, 2004). S. HAMPSHIRE [11] Gosport, 17.10 (47) (D. Tinling). W. SUSSEX [13] Thomey Island, 3.10 (23) (T. Wilson per CRP). E. SUSSEX [14] Cuckmere Valley, 18.10 (24) (DB per CRP). E. NORFOLK [27] Nr. Hockwold, 2.8 (20+), in a Lucerne field (P. Laurie). W. CORK [H3] Dursey Island, 26.9 (29) (Scott, 2004b). Most northerly records: ISLE OF MAN [71] Dhoon Maughold, 15.7 (per GDC). Selected inland records: SURREY [17] Camberley, 15.9 (GAC); Chiddingfold, 17.10 (GAC); Lambeth Reservoir, 26.7 (3) (S.J. Spooner per SN). MIDDLESEX [21] Tottenham Marshes, 31.5 (per L. Goodyear via SN). CAMBRIDGESHIRE [29] Wicken, 15.10 (2) (DEW). HUNTINGDONSHIRE [31] Bluntisham Fen, 3.8, 29.8, 31.8 (B «& J. Milne per BD); near Hemmingford Abbots, 17.8 (M. Everett per BD); near Huntingdon, 20.7 (B & J. Milne per BD), 25.9 (S. Smith per BD); Orton Southgate, 4.9 (N. Crossman per BD); near Peterborough, 2.8, 14.9 (A. Frost per BD); Sapley, 2.8 (NG- D per BD); St Ives, 6.7 (B & J. Milne per BD); near St Neots, 21.7 (J. Stevenson per BD); Warboys, 15.6 (P. Rowlings per BD); Weaveley Wood, 2.8 (A. Booth per BD). WORCESTERSHIRE [37] Nr. Longbridge, 3.8 (R. Wardle). WARWICKSHIRE [38] Nr. Newbold upon Stour, 3.8 (2) (N. Stone). LEICESTERSHIRE [55] 25+ adults recorded across the county, 6.5 - 3.9 (per APR). CHESHIRE [58] Nr. Northwich, 29.5 (S. Hefferan per SF). S.W. YORKSHIRE [63] Uppermill, 13.9 (P.B. Hardy per SHH). Evidence of breeding: S.E. YORKSHIRE [61] Spurn Point, 27.7, ovipositing female (C. Bowler per SN). NYMPHALIDAE 1590 Vanessa atalanta (L.) Red Admiral [R][I] Selected annual totals: W. CORNWALL [1] lOS: St Mary’s, Longstone - 1256 (Scott, 2004a). DORSET [9] West Bexington - 193 (Eden, 2004). E. SUSSEX [14] Peacehaven - 497 (Pratt, 2004). S. ESSEX [18] Bradwell-on-Sea - 2684 (Dewick, 2004). PEMBROKESHIRE [45] Skomer Island - 4545 (Hayden, 2004). CHESHIRE [58] County total - 699 (per SF). BANFFSHIRE [94] Ordiquhill - 121 (Rl2). Earliest dates (active): E. CORNWALL [2] Delabole, 16.1 (anon.). S. HAMPSHIRE [11] Colden Common, 16.1 (R. Rowe); Portchester, 16.1 (IS). N. HAMPSHIRE [12] Hook, 16.1 (A. McCue). W. CORK [H3] Near Schull, 4.1 (N. Addey per IR). ANTRIM [H39] Belfast, 16.1 (G. Saunders per IR). Latest dates (active): Bochym, The Lizard, 17.12 (Tunmore, 2004). DORSET [9] Bridport, 18.12 (per MSP). S. HAMPSHIRE [11] Gosport, 21.12 (D. Tinling). MIDDLESEX [21] Alexandra Palace, Wood Green, 18.12 (M. Conway). W. SUSSEX [13] Selsey, 18.12 (SIP). E. SUSSEX [14] Seaford. 17.12 (2) (S. Fletcher per SN). Large counts: W. CORNWALL [1] lOS: St Mary’s, Longstone, 30.8 (170) (Scott, 2004a). S.E. YORKSHIRE [61] Spurn, 24.9 (250) (BRS). S. ESSEX [18] Bradwell-on-Sea, 31.7 (115), 2.8 (116) (Dewick, 2004). PEMBROKESHIRE [45] Skomer Island, 25.8 (1500) (Hayden, 2004). W. CORK [H3] Dursey Island, 26.9 (120) (Scott, 2004b). Light-trap records: W. CORNWALL [1] lOS: St Mary’s, Longstone, 30.6 - 18.10 (33), including 13 on 27.9 (Scott, 2004a); The Lizard, August (1), September (5) (Tunmore, 2004). S. DEVON [3] Branscombe, 14.6 (BPH, RFM). DORSET [9] Portland Bird Observatory, 30.6 - 29.9 (12) (Cade, 2004). S. ESSEX [18] Bradwell-on-Sea, 1.8, 5.8 (2), 6.8, 10.8, 12.8 (2), 13.8, 16.8, 10.9, 20.9, 1.10 (Dewick, 2004). Immature stages/Evidence of breeding: W. CORNWALL [1] Mevagissey, 25.10, pair in cop. (Ofield, 2004). BANFFSHIRE [94] Nr. Macduff, 23.7, larvae abundant (RL^). 1591 Vanessa cardui (L.) Painted Lady [I] Selected annual totals: W. CORNWALL [1] lOS: St Mary’s, Longstone - 995 (Scott, 2004a). DORSET [9] West Bexington - 137 (Eden, 2004). E. SUSSEX [14] Peacehaven - 215 (CRP). E. KENT [15] Dungeness Bird Observatory - 1048 (DW). S. ESSEX [18] Bradwell-on-Sea - 5240 (Dewick, 2004). PEMBROKESHIRE [45] Skomer Island - 6791 (Hayden, 2004). CHESHIRE [58] County total -461 (perSF). Earliest dates (active): W. CORNWALL [1] The Lizard, 17.3 (Tunmore, 2004). E. CORNWALL [2] Near Torpoint, 16.3 (2) (D. Allen). S. DEVON [3] Plymouth, 12.3 (VT), 14.3 (2) (S. Coombes); Stoke Point, 15.3 (6), 16.3 (VT). S. SOMERSET [5] Taunton, 13.3 (M. Ridge). DORSET [9] St Aldhelm’s 2003 IMMIGRATION REVIEW 27 Head, 17.3 (RL); West Bexington, 14.3 (Eden, 2004). E. KENT [15] Isle of Thanet, 24.3 (Solly, 2004). W. CORK [H3] Dursey Island, 12.3 (Scott, 2004b). Latest dates (active): W. CORNWALL [1] lOS: St Mary’s, Longstone, 9.11 (Scott, 2004a). S. DEVON [3] Buckfastleigh, 10.11 (B&LB per REM). E. SUSSEX [14] Elms Farm, Icklesham, 4.11 (Hunter, 2004). E. KENT [15] Isle of Thanet, 4.11 (Solly, 2004). Large counts: W. CORNWALL [1] lOS: St Mary’s, Longstone, 31.8 (100) (Scott, 2004a). S. DEVON [3] Between Start Point & Torcross, 28.6 (300+) (M. Catt). DORSET [9] Portland, June (100+ on many dates), August (many hundreds daily) (Cade, 2004). W. SUSSEX [13] Pagham, 24.7 (large numbers, inc. 100+ in one field) (SIP); Pulborough, 26.7 (c.200) (per CRP). E. SUSSEX [14] Elms Farm, Icklesham, 22.7 (c. 150,000) (Hunter, 2004); Hollingbury, 3.8 (c.200) (per CRP). E. KENT [15] Oare, 20.7 (c.200) (S. Nunn per ME); Ramsgate Hoverport, 31.7 (c.2000) (Solly, 2004); Sandwich, 2.8 (104 on transect) (P. Forrest); Thanet, 3.8 (182 at two sites) (S. Blaskett per ME). S. ESSEX [18] Bradwell- on-Sea, 27.7 (415), 28.7 (577), 29.7 (627), 30.7 (658), 31.7 (646) (Dewick, 2004). N. ESSEX [19] Nr. Halstead, 26.7 (500) (per SN); Markshall, 29.7 (789) (D. Owen); Marks Tey, 24.7 (several hundred) (N. Harvey); Walton-on-the-Naze, 28.7 (277) (D. Owen). E. SUFFOLK [25] Aldeburgh, 3.6 (100 in one field) (per RP); (Bawdsey, 27.7 (360) (C.A. Jacobs); Culpho, nr. Ipswich, 1.6 (400) (per RP); Landguard, 3.6 (150) (per SHP); Thorpeness, 2.6 (200) (C.A. Jacobs). E. NORFOLK [27] Nr. Hockwold, 2.8 (8000), in a Lucerne field (P. Laurie). N. LINCOLNSHIRE [54] Gibraltar Point, 28.7 (300+) (Sykes, 2004). S.E. YORKSHIRE [61] Spurn, 2.6 (140), 16.7 (169), 2.8 (475), 12.9 (420) (BRS). PEMBROKESHIRE [45] Skomer Island, 25.8 (3000) (Hayden, 2004). LEICESTERSHIRE [55] Edith Weston, 2.8 (c.200) (V. Arnold). NOTTINGHAMSHIRE [56] Eakring, 3.8, (715) (T. Pendleton). W. CORK [H3] Dursey Island, 26.9 (120) (Scott, 2004b). Light-trap records: W. CORNWALL [1] lOS: St Mary’s, Longstone, 5.7 - 25.9 (7), including four on 6.8 (Scott, 2004a); The Lizard, 23.3, September (3) (Tunmore, 2004). S. DEVON [3] Branscombe, 14.6 (BPH, RFM). DORSET [9] Portland Bird Observatory, 1.8 - 25.9 (4) (MC). S. ESSEX [18] Bradwell- on-Sea, 30.7 (4), 1.8 (2), 2.8 (4), 3.8, 4.8, 5.8, 6.8 (2) (Dewick, 2004). HUNTINGDONSHIRE [31] Woodwalton Fen, 2.8 (BD). ISLE OF MAN [71] Dhoon Maughold, 2.9 (per GDC). Immature stages: W. CORNWALL [1] Crantock, 11.7, larva on Borago ojficinalis (KNAA). S. DEVON [3] South Milton Sands, 16.8, two larvae on Arctium spp. (BPH). DORSET [9] West Lulworth, 18.7, larva on Arctium minus (DH^ per SPC). ISLE OF WIGHT [10] Bonchurch, larvae in June (JH). E. SUSSEX [14] Rye Harbour, July, undated, larva on Artemisia vulgaris (DB per SPC). E. KENT [15] Dungeness, 17.7, larva on Plantago lanceolata (SPC). SURREY [17] Guildford, 10.6, larva (GAC). MIDDLESEX [21] Shepperton, 21.7, larva (GAC). CAMBRIDGESHIRE [29] Wicken, July & August, larvae common (DEW). HUNTINGDONSHIRE [31] Bluntisham Fen, 14.6, larva(e) (B & J. Milne per BD). LEICESTERSHIRE [55] Empingham, 11.8, larvae (M.W. Tyler per APR). CHESHIRE [58] Manchester airport, 25.6, larva (I.F. Smith per SF); West Kirby, 7.7, larva (I.F. Smith per SF). BANFFSHIRE [94] Ordiquhill, 24.8, larva and vacated webs (RL^). SHETLAND ISLANDS [112] Norwick, 13.8, larva (M. Mouat). GEOMETRIDAE 1716 Rhodometra sacraria (L.) Vestal [I] Total no. reported: 1067 Distribution of records: sw cs SE EA SI W CE NE NW S I 627 283 66 5 24 18 13 1 4 - 26 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec - - - - - 14 17 165 432 252 14 - Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 140 (MEH, AD); lOS: St Mary’s, Longstone - 264 (Scott, 2004a); The Lizard - 109 at three sites (Tunmore, 2004). DORSET [9] Bridport area - 45 at two sites (Parsons & Brereton, 2004); Portland Bird Observatory - 40 (Cade, 2004); West Bexington - 29 (Eden, 2004). ISLE OF WIGHT [10] Approximate Island total - 30 (Knill- Jones, 2004). W. SUSSEX [13] Selsey - 24 at three sites (Patton, 2004); Walberton - 20 (JTR per CRP). E. KENT [15] Dungeness area - 20 at eight sites (per SPC). Ealiest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 27.6 (Scott, 2004a). N. DEVON [4] Bideford, 26.6 (2) (ASH per RFM). DORSET [9] Preston, 26.6 (MF). ISLE OF WIGHT [10] Totland, 28 ENTOMOLOGIST’S RECORD, VOL. 119 25.1.2007 26.6 (SAK-J). E. KENT [15] New Romney, 26.6 (SPC); Isle of Thanet, 27.6 (Solly, 2004). WARWICKSHIRE [38] Charlecote, 22.6 (DCGB). GLAMORGAN [41] Mumbles, 25.6 (T. Bantock per SN). BRECONSHIRE [42] Newbridge-on- Wye, 24.6, by day (G. Tordoff per SN). Latest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 20.11 (Scott, 2004a). WICKLOW [H20] Ashford, 17.11 (2) (AT). Large single night counts: W. CORNWALL [1] Coverack, The Lizard, 12.10 (8) (DCGB); lOS: St Agnes, 12.10 (16), 13.10 (27) (Davison, 2004); lOS: St Mary’s, Longstone, 30.8 (18), 12.10 (21) (Scott, 2004a). Most northerly records: CHESHIRE [58] Halton, 17.9 (J.J. Clarke per SF). W. LANCASHIRE [60] Lightfoot Green, 18.9 (SMP). S.E. YORKSHIRE [61] Easington, 21.9 (M.J. Stoyle per BRS). ISLE OF MAN [71] Dhoon Maughold, 18.9, 22.9 (per GDC); Minorca Laxey, 24.9 (per GDC). Selected inland records: N. HAMPSHIRE [12] Grateley, 20.9, 10.10, 14.10 (S. Colenutt per TN); Grey well, 26.9, 16.10 (P. Boswell per TN); Selbome, 20.9 (3), 1.10 (AEA). SURREY [17] Banstead, 6.8 (S.W. Gale per GAC); Ewell, 24.9 (GAC). S. ESSEX [18] Epping Forest, August, undated (T. Green per BG); Magdalen Laver, September, undated (T. Green per BG). N. ESSEX [19] Felsted, 21.7 (G. Geen per BG); Takeley, 22.9 (G. Sell per BG). HERTFORDSHIRE [20] Bishops Stortford, 21.9 (JF per CWP); Hertford, 21.9 (AW per CWP); Ware, 20.9 (EG per CWP). BERKSHIRE [22] Dry Sandford, 21.9 (AK); Fernham, 2.7, 3.8 (SN). CAMBRIDGESHIRE [29] Wicken, 30.9 (DEW). BEDFORDSHIRE [30] Cockayne Hatley, 5.9 (I.P. Woiwood per LH). HUNTINGDONSHIRE [31] Kimbolton, 17.10 (T. Parnell per BD). WARWICKSHIRE [38] Charlecote, 22.6, 17.8, 19-29.9 (4), 2.10, 13.10 (DCGB). LEICESTERSHIRE [55] Barrowden, 14.8 (R. Follows per APR); Dadlington, 9.10 (3) (R. Smith per APR); Eyebrook Reservoir, 2.8, 19.9 (R. Follows per APR). 1720 Orthonama obstipata (Fab.) Gem [I] Total no. reported: 446 Distribution of records: sw cs C/3 m 1 EA SI w CE i i NE NW S I 160 155 l_ZL_ 4 4 5 9 1 12 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 3 4 6 7 IQ- 36 89 70 80 61 4 Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 43 (MEH, AD); lOS: St Mary’s, Longstone - 67 (Scott, 2004a); The Lizard - 22 at three sites (Tunmore, 2004). DORSET [9] Portland Bird Observatory - 39 (Cade, 2004). ISLE OF WIGHT [10] Total from two sites - 14 (JH, SAK-J). W. SUSSEX [13] Walberton - 14 (JTR per CRP). E. KENT [15] Dungeness area - 32 at nine sites (per SPC). Ealiest dates: W. CORNWALL [1] lOS: St Agnes, March, undated (2) (Hicks, 2004); lOS: St Mary’s, Longstone, 28.3 (Scott, 2004a). CARMARTHENSHIRE [44] Wharley Point, 18.4 (J. Baker). Latest dates; W. CORNWALL [1] lOS: St Agnes, December, undated (2) (Hicks, 2004); lOS: St Mary’s, Longstone, 14.12, 18.12 (Scott, 2004a). DORSET [9] Walditch, 29.11 (MSP). W. SUSSEX [13] Walberton, 30. 1 1 (JTR per CRP). Large single night counts: W. CORNWALL [1] Coverack, The Lizard, 13.10 (12), 15.10 (5) (DCGB); lOS: St Agnes, 13.10 (5) (Davison, 2004); lOS: St Mary’s, Longstone, 13.10 (6) (Scott, 2004a). DORSET [9] Portland, 5.9 (13) (MC); Studland, 5.9 (4) (DCGB). W. CORK [H3] Cape Clear Island, 12.10 (6) (per KB). Most northerly records: S. LANCASHIRE [59] St Helens, 28.10 (C. Davies per SMP). S.E. YORKSHIRE [61] Kilnsea, 18.7 (PAC), 1.10 (BRS); Spurn 10.7, 2.10 (BRS). ISLE OF MAN [71] Dhoon Maughold, 1.9, 2.9, 18.9, 20.9, 30.9 (per GDC); Gob y Volley Ballaugh, 14.6 (per GDC). SHETLAND ISLANDS [112] Eswick, 12.11 (TR). Selected inland records: N. HAMPSHIRE [12] Selbome, 4.6, 6.6, 14.8, 15.8 (AEA). E. SUSSEX [14] Crawley Down, 2.10, 19.11 (JHC per CRP). SURREY [17] Chobham, 15.7 (PR. Wheeler per GAC); West Molesey, 2.7 (PR. Williams per GAC). HERTFORDSHIRE [20] Bishops Stortford, 15.6 (JF, J. Reeves); Harpenden, 18.1 1 (PG per CWP); Long Marston, 26.6 (P. Bygate per CWP); Marshalls Heath, 2.7 (J. Murray). BERKSHIRE [22] Dry Sandford, 30.10 (AK). E. NORFOLK [27] Scole, 13.8 (M. Hall per DH). HUNTINGDONSHIRE [31] Grafham Water, 20.9 (BD); Huntingdon, 1.10, 3.10 (M. Shardlow per BD); Kings Ripton, 23.8 (D. Ritchie per BD); Yaxley, 5.9 (A. Frost per BD). WARWICKSHIRE [38] Hillmorton, Rugby, 4.8, 7.8 (D. Porter per DCGB). DERBYSHIRE [57] 2003 IMMIGRATION REVIEW 29 Foremark Reservoir, 18.11 (Budworth et al, 2004). LEICESTERSHIRE [55] Braunstone, 7.5 (L. Holton per APR). S. LANCASHIRE [59] Chorlton, 18.11 (B. Smart per SMP). S.W. YORKSHIRE [63] Holdworth, Sheffield, 11.11 (K. Clarkson). SPHINGIDAE 1972 Agrius convolvuli (L.) Convolvulus Hawk-moth [I] [In] Total no. adults reported: 2671 Distribution of records: sw cs SE EA SI W CE NE NW S I 1361 763 277 74 31 35 27 20 21 34 28 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec - - - - - 7 27 659 602 71 2 - Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 140 (Hicks, 2004); lOS: St Mary’s, Longstone - 172 (Scott, 2004a); lOS: St Mary’s, August & September, island total - 1000+ (Scott, 2004a); The Lizard - 46 at three sites (Tunmore, 2004). DORSET [9] Portland Bird Observatory - 136 (Cade, 2004); Puddletown - 61 (HWH); West Bexington - 122 (Eden, 2004). ISLE OF WIGHT [10] Approximate Island total - 138 (Knili-Jones, 2004); Bonchurch - 40+ (JH); Totland - 35 (SAK-J). S. HAMPSHIRE [11] Wickham Common, Fareham - 11 (Coker, 2004). W. SUSSEX [13] Ferring - 1 1 (THF per CRP); Walberton - 10 (JTR per CRP). E. SUSSEX [14] Peacehaven - 14 (CRP). E. KENT [15] Dungeness area - 40 at twelve sites (per SPC); Isle of Thanet - 84 at seven sites (Solly, 2004). S. ESSEX [18] Bradwell-on-Sea - 24 (Dewick, 2004). S.E. YORKSHIRE [61] Spurn area - 8 at three sites (BRS, PAC). ISLE OF MAN [71] Island total - 17 (Craine, 2004). W. CORK [H3] Crookhaven, 14-19.9 (11) (Allen & Mellon, 2004). Ealiest dates: W. CORNWALL [1] The Lizard, June, undated (Tunmore, 2004). N. DEVON [4] Hartland Point, 22.6 (BPH, REM). DORSET [9] Durlston, 26.6 (PAD, SN); West Bexington, June (undated) (Eden, 2004). E. SUFFOLK [25] Landguard Bird Observatory, 17.6 (Odin, 2004). S.E. YORKSHIRE [61] Kilnsea, 29.6 (PAC). Latest dates: W. SUSSEX [13] Ringmer, 30.10 (A. Batten per CRP). S. ESSEX [18] Rainham Marshes, 15.11 (N.R. Bruce- White per BG). NOTTINGHAMSHIRE [56] Kimberley, 8.11, found dead (I. Cook per JE). Large single night counts: W. CORNWALL [1] lOS: St Agnes, 27.8 (24), late August, up to 10 feeding at Oenothera biennis flowers (Hicks, 2004); lOS: St Mary’s, Longstone, 17.8 (11) (Scott, 2004a); lOS: St Mary’s, late August, undated (30), feeding together at Hedychium spp. flowers (Scott, 2004a); St Delian, near Penzance, 25.9 (6) (J. Yamold per PHB). S. DEVON [3] Hope Cove, Kingsbridge, 11.8 - 6.9, up to 9 per night feeding at Lonicera spp. Flowers (K. Trout per RFM). DORSET [9] Durlston, 7.8 (17) (JMc), 5.9 (33) (DCGB), 19.9 (39) (SN). GLAMORGAN [41] Kenfig NNR, 23.8 (7) (Gilmore, 2004). Most northerly records: N. ABERDEENSHIRE [93] Auchnagatt, 4.7 (C. Harlow); Huntly, 10.9 (per P. Shand via RL^). BANFFSHIRE [94] Comhill, 4.9 (J. McLeod per RL^). MORAY [95] New Elgin, 11.9 (D. Jamieson per RL^). SHETLAND ISLANDS [112] Burrafirth, 13.8 (anon.); Eswick, 8.8, 16.8 (T. Rogers); Fair Isle, 13.9 (anon.); Fetlar, 6.9 (2), 8.9 (2) (anon.), 10.9 (K. & M. Hughson); Foula, 1.8 (2), 5.8 (2), 26.8 (2), 27.8, 4.9 (G. & D. Atherton); Kirkadale, 13.8, by day (per R. Ditchbum); Lerwick, 15.8, 17.8 (anon.); Mid Yell, 11.9 (4+) (anon.); Norwick, 18.8 (W. & H. Laurenson); Unst, 22.8 (R. & W. Henderson); Urafirth, 18.8 (anon.); Whalsay, 16.9 (anon.). Selected inland records: SURREY [17] Givons Grove, near Leatherhead, 14.8 (A.M.V. Hoare per GAC). HERTFORDSHIRE [20] Bishops Stortford, 20.9 (J. Horrocks per CWP); Long Marston, 14.8 (P. Bygate per CWP); Quickswood, 19.8 (E. May per CWP), 16.9 (D. Heath per CWP); Shenley, 30.8 (W & P. Page per CWP). MIDDLESEX [21] Alexandra Palace, 6.8 (G. Newbiggin per CWP). BERKSHIRE [22] Dry Sandford, 6.8, 26.8 (AK). BEDFORDSHIRE [30] Bedford, 30.8 (B. Anderson per LH); Haynes, 26.8 (S. Rowe per LH); Luton, 7.8, 15.8, 16.9 (H. Palmer per LH); Potton, 24.8 (A. Darrington per LH); Odell, 3.9 (H.A. Smith per LH); Whipsnade, 1.9 (C. Tack per LH). HUNTINGDONSHIRE [31] Abbots Ripton, 8.9 (C. Drage per BD); Easton, September, undated (B. Davis per BD); Houghton, 13.8 (per BD); Huntingdon, 10.9 (M. Abbot per BD); Kings Ripton, 5.9 (D. Ritchie per BD); Stow Longa, September, undated (W. Caress per BD). WARWICKSHIRE [38] Norton Lindsey, 31.8 (H. Cuttell per DCGB); Pillerton Priors, 18.8 (C. Ivin per DCGB). STAFEORDSHIRE 30 ENTOMOLOGIST’S RECORD, VOL. 119 25.1.2007 [39] Solihull, 4.8 (B. Moore per SN), West Bromwich, 4.8 (S. Flower per SN). LEICESTERSHIRE [55] Asfordby, 19.9 (A. Corley per APR); Barrowden, 26.8 (L. Worrall per APR); Birstall, 22.8 (J. Williams per APR); Cottesmore, August, undated (per APR); Earl Shilton, 15.8 (C. Baggott per APR); Fleckney, 16.9 (J.G. Cranfield per APR); Glen Parva, 14.8 (per APR); Goadby, 10.8, 12.8, 19.8 (per APR); Hinckley, 15.8 (D. Taylor per APR); Hugglescote, 2.10 (K.K. Ingram per APR); South Luffenham, 29.8 (L. Worrall per APR); Thorpe Satchville, 18.9 (F.J. Johnson per APR); Wigston, 20.8 (R. Felce per APR). NOTTINGHAMSHIRE [56] Edwinstowe, 15.7 (T. Barton per SW); Flintham, 8.9 (J. Lennon per SW); Kimberley, 8.11 (I. Cook per JE); Kirkby-in-Ashfield, 2.10 (S. Kelly per IE); South Leverton, 23.8 (Y. Winder per SW). DERBYSHIRE [57] Whitwell Wood, 23.8 (Budworth et al, 2004); Matlock, 21.9 (Budworth et al, 2004). W. LANCASHIRE [60] Colne, 7.8 (per SN). S.E. YORKSHIRE [61] Haxby, 24.9 (per TE); Hook, near Goole 7.9 (2) (R. Butcher per BRS). ARMAGH [H37] Portadown, 19.8 (D. Cornett per IR). Immature stages: W. CORNWALL [1] Falmouth, 10.10, larva (S. Dunbar per PHB); lOS: St Agnes, c. 10 larvae (Hicks, 2004); lOS: St Mary’s, c.200 larvae reported (Scott, 2004a); Land’s End, 11.10, larva (Boggis, 2003); Marazion, 11.10, larva (Boggis, 2003); Nanquidno Valley, 12.10, eight larvae (Boggis, 2003); Penzance area, early September, 20+ larvae (R. Sadler et al per PHB); Porthcurno, 11.10, larva (Boggis, 2003); Porthgwarra, 11.10, three larvae (Boggis, 2003); Praa Sands, 12.10, two larvae (Boggis, 2003); The Lizard, September/October, ‘high numbers of larvae’ (Tunmore, 2004); Sennen, 11.10, five larvae (Boggis, 2003); St Columb Major, 2.10, larva (PHB); Trevose Head, 21.9, larva (D.I. Julian per PHB). E. CORNWALL [2] Portmellon, 27.8, larva (B. Ofield per PHB); near Saltash, 2.8, larva (I. Bennallick per JH^); Torpoint, 8.10, larva (Boggis, 2003). S. DEVON [3] Nr. Start Point, 25.8, nine ova & two larvae (BPH); Wembury, 19.9, larva (T. Sleep per RFM). DORSET [9] Blandford, 13.9, larva (N. Butt); Chilcombe, 5.9, two larvae (J. d’Erlanger); Portland, September/October, larvae found at several sites (Cade, 2004); Seacombe, 15.9, five larvae (PAD); Walditch, 30.9, larva (MSP); Wareham, 21.9, larva (A. Stewart); West Bexington, 25.9, larva (Eden, 2004). ISLE OF WIGHT [10] Along the south coast of the island, 12+ larvae reported (Knill-Jones, 2004); Bonchurch, mid-September, larva (JH); St Catherine’s Point, mid-September, larva (JH). W. SUSSEX [13] Cross Bush, mid-October, pupa inside greenhouse (per CRP); Ferring, 13.9, larva (J. Kennedy per CRP); Plaistow, larva, pupated in October (per CRP). E. SUSSEX [14] Bevendean, 3.10 (C. Downs per CRP); Brighton, 15.9, larva (A. Stevens per CRP); Horns Cross, October, eight larvae (DB per CRP); Northiam, 1.10, larva (A. Lee per CRP); Peacehaven, 19.9, two larvae (K. Robinson per CRP); Rye Harbour, 27.9, larva (B. Yates per CRP). E. KENT [15] Dungeness, 24.9, twelve larvae (D. Bunny per SPC). N. ESSEX [19] Bradfield, September, larva (I. Rose per BG); Old Hall Marshes, 23.8, larva (C. Tyas per BG). E. SUFFOLK [25] Minsmere, 22-24.9, larva (Harvey, 2004). W. SUFFOLK [26] Whepstead, 4.9, larva (A. Read per AWP). GLAMORGAN [41] Bridgend, 28.9, larva(e) (Gilmore, 2004); Cheriton, 7.10, larva(e) (Gilmore, 2004); Cwm Ivy, 24.9, 25.9, 28.9, 29.9, at least six larvae in total (VS); Langley Bay, 6.10, larva(e) (Gilmore, 2004); Llanmadoc, 29.9, 2.10, larvae (Gilmore, 2004); Neath, 3.10, larva(e) (Gilmore, 2004); Pontcanna, 3.10, larva(e) (Gilmore, 2004); Pwll, Llanelli, 3.10, two larvae (R.D. Price); Rhossili, 12.10, larva(e) (Gilmore, 2004); St Donat’s, 24.9, larva(e) (Gilmore, 2004); Tremorfa, September, larva(e) (Gilmore, 2004). CHESHIRE [58] North Wirral, 3.10, larva (P. Bowler per SF); Wallasey, 4.9, three larvae (D.C. Hinde per SF). S.E. YORKSHIRE [61] Kilnsea, 25.8, pupa dug up (P. Martin); Spurn area, five larvae found between 26.8 & 7.10 (BRS). ISLE OF MAN [71] Minorca Laxey, 19.9, larva (per GDC). Importation: W. SUSSEX [13] Littlehampton, 31.1, on the side of a refrigerated lorry from South Africa (per CRP). 1984 Macroglossum stellatarum (L.) Humming-bird Hawk-moth [I] Minimum no. adults reported: 5400+ Selected annual totals: W. CORNWALL [1] lOS: St Mary’s, Longstone - 323 (Scott, 2004a). ISLE OF WIGHT [10] Approximate Island total - 200 (Knill-Jones, 2004). E. SUSSEX [14] Hampden Park, Eastbourne - c.lOO (R. Mellor per CRP); Peacehaven - 68 (CRP); Woodingdean - 212 (R. Musselle per CRP). E. KENT [15] Dungeness area - 164 at ten sites (per SPC). S. ESSEX [18] Bradwell-on-Sea - 370 (Dewick, 2004). PEMBROKESHIRE [45] Skomer Island - 51 (Hayden, 2004). S.E. YORKSHIRE [61] Spurn area - 163+ (BRS, PAC, P. Martin). ISLE OF MAN [71] Island total - 23 (per GDC). W. CORK [H3] Dursey Island - 70+ (Scott, 2004b). Non-specific comments: W. CORNWALL [1] Constantine, Falmouth, large numbers between 23.6 & 7.7 (H. Jonas per RDP); The Lizard, present in abundance during the summer and autumn months (Tunmore, 2004). DORSET [9] Portland, numerous by day throughout the island (recorded between 8.6 & 2.12) (Cade, 2004). ISLE OF WIGHT [10] Bonchurch, very common during the week of 18.8 (JH). S. HAMPSHIRE [11] 147+ adults recorded across the VC (perTN). N. HAMPSHIRE [12] 100+ adults recorded across the VC (per TN). ESSEX [18 & 19] A very good year, reported from forty-eight sites. 2003 IMMIGRATION REVIEW 31 mostly from June to October with a peak in mid-August (per BG). HERTFORDSHIRE [20] 19.3 - 27.11, 171 adults recorded across the county (per CWP). CAMBRIDGESHIRE [29] Wicken, 20.6, then regular until end of August (DEW). BEDFORDSHIRE [30] 9.6 - 27.11, 130+ adults reported across the county (per LH). HUNTINGDONSHIRE [31]13.6 - 15.10, 83+ adults reported across the county (per BD). LEICESTERSHIRE [55] 9.6 - 30.10, 180+ adults reported across the county (per APR). NOTTINGHAMSHIRE [56] 11.6 - 10.10, 52+ adults reported across the county (per SW & IE). DERBYSHIRE [57] 13.6 - 18.10, 38+ adults reported across the county (Budworth et al, 2004). CHESHIRE [58] 7.6 - 11.11, 56+ adults reported across the county (per SF). LANCASHIRE [59 & 60] The first influx occurred in mid to late June, the moth being recorded widely throughout the county over the following few weeks. Then daily sightings throughout July and again during September (per SMP). Earliest dates (active): E. CORNWALL [2] Launceston, 7.3 (J. Dowlman). EAST KENT [15] Pedlinge, 27.1 (S. Scrivens). HERTFORDSHIRE [20] Datchworth, 19.3 (A. Fisher per CWP); Digswell, 20.3 (T. Gladwin per CWP). MIDDLESEX [21] Enfield, 18.3 (per CWP). CAERNARVONSHIRE [49] Lleyn Peninsula, 13.3 (L. Hewitt). Latest dates (active): S. SOMERSET [5] Taunton, 3.12 (J.C. Lidgate). DORSET [9] Portland, 2.12 (Cade, 2004). ISLE OF WIGHT [10] Freshwater, 15.12 (A. Butler per SAK-J). MIDDLESEX [21] Highgate Road, London, 21.12 (anon.). W. CORK [H3] Dursey Island, 6.12 (Scott, 2004b). Large counts: W. CORNWALL [1] Constantine, Falmouth, 30.6 (24+) (H. Jonas per RDP); lOS: St Mary’s, Longstone, 27-31.8 (74), including 21 on 28.8 (Scott, 2004a); Pendennis Castle, Falmouth, 23.6 (50) (R. Parslow). DORSET [9] Portland, August, 100+ on many dates (Cade, 2004). E. SUSSEX [14] Willingdon, 11.7 (12+, seen together probing chalk) (R. Mellor, S. Young per CRP). E. KENT [15] Dungeness Bird Observatory, 21.8 (15) (DW); Isle of Thanet, up to 10 daily in August (Solly, 2004). W. KENT [16] Otford, 24.6 (c.50) (Ferguson, 2005). S. ESSEX [18] Bradwell-on-Sea, 13.8 (32), 10-21.8 (double figure counts on nine days) (Dewick, 2004). S.E. YORKSHIRE [61] Kilnsea, 28.6 (7) (P. Martin). W. CORK [H3] Dursey Island, 26.9 (14) (Scott, 2004b). MID CORK [H4] Roche’s Point, 21/22.6 (20) (T. Gittings per IR). Most northerly records: ROXBURGHSHIRE [80] Harestanes, near Jedburgh, 3.9 (JW). BERWICKSHIRE [81] Milldown Point, 1.10 (JW). MIDLOTHIAN [83] Edinbugh, 13.11 (per SN). SHETLAND ISLANDS [112] Burravoe, 2.7 (D. & H. Thomson); Fair Isle, 13.9 (anon.); Hermaness, 14.6 (anon.); Muckle Roe, 15.8 (anon.); Outer Skerries, 20.9, 17.10 (2) (anon); Whalsay, 22.6 (B. & L. Marshall). Light-trap records: W. CORNWALL [1] The Lizard, 30.8, 17.9, 20.9, 13.10 (Tunmore, 2004). S. DEVON [3] Teignmouth, 22.8 (RFM). DORSET [9] Canford, 30.9 (P. Taylor); Durlston, 19.9, 20.9 (SN, PAD); Portland Bird Observatory, 2.6 - 21.9 (29) (Cade, 2004); Preston, 5.6 (MF); Southwell, 13.9 (2) (JHC); Walditch, 7.9 (MSP); West Bexington, 23.6 (2), 25.6, 3.9 (RE); Weymouth, 30.6 (PHS); Wool, 19.9 (D. Cooper); Wyke Regis, 11.6, 14.6, 4.9 (2), 17.9 (DF). ISLE OF WIGHT [10] Bonchurch, around 18.8 (JH). W. SUSSEX [13] Pagham, 5.11 (JHC). E. SUSSEX [14] Elms Farm, Icklesham, 21.10 (Hunter, 2004); Heathfield, 21.9 (DRML per CRP). E. KENT [15] Dungeness area, June - October (14+, including 3 at the Bird Observatory on 5.9 & 21.9 (DW)) (per SPC); Isle of Thanet, undated (5 in total) (Solly, 2004); Sandwich, 10.6 (D. Wrathall). E. SUFFOLK [25] Landguard Bird Observatory, 26.7, 13.10 (Odin, 2004). E. NORFOLK [27] Eccles-on-Sea, 25.6, 30.6, 29.6, 12.9, 20.9 (NB per DH). BEDFORDSHIRE [30] Carlton, 17.9 (H.A. Smith per LH); Potton, 27.8 (H.A. Smith per LH); Studham, 18.9 (C.R.B. Baker per LH); Turvey, 3.9 (H.A. Smith per LH); Yelden, 13.10 (A. Paynter per LH). HUNTINGDONSHIRE [31] Earith, 14.6 (D. Griffiths per BD); Folksworth, August (1), September (1) (A. Frost per BD); Yaxley, July (1), August (1) (A. Frost per BD). S.E. YORKSHIRE [61] Spurn, 9.8 (BRS). Evidence of hibernation: E. SUSSEX [14] Brighton, 10.1, 18.11, singletons at rest inside Royal Sussex County Hospital (J. Paul). GLAMORGAN [41] Paviland Cave, 27.10, prospecting inside cave. Immature stages: DORSET [9] Badbury Rings, 9.7, four larvae (PAD); Coombe Valley, 13.7, 3.8, larvae (MF); Lulworth Cove, 18.7, three larvae (MSP); Portland, 10.7, thirteen larvae (RRC), 31.7, two larvae (MSP). E. SUSSEX [14] Camber, larvae during July (DB per CRP); Hope Gap, late July, thirteen larvae found in 15 minutes (AJB per CRP); Seaford Head, larvae during July (DB per CRP); Woodingdean, undated, two larvae (K. Robinson per CRP). S. ESSEX [18] Bradwell-on-Sea, forty-six larvae during July, 25.8 (larva) (Dewick, 2004). E. SUFFOLK [25] Beccles, 31.7, larva (M. Mayston per AWP); Felixstowe, undated, larva (B. Matthews per AWP). DERBYSHIRE [57] Bolehill, 22.7, larva (B.L. Statham, in Budworth et al, 2004); Bonsall Moor, 22.7, two larvae (B.L. Statham, in Budworth et al, 2004); Matlock, 22-25.7, nine larvae (B.L. Statham, in Budworth et al, 2004). S. LANCASHIRE [59] Liverpool, 18.7, c.25 larvae at the National Wildflower Centre (D. Young per SMP); Walton, 4.8, larva (M. Pons per SMP). 32 ENTOMOLOGIST'S RECORD, VOL. 119 25J.2007 NOCTUIDAE 2091 Agrotis ipsilon (Hufn.) Dark Sword-grass [I] Total no. reported; 10747 Distribution of records; sw cs SE EA SI W CE NE NW S I 2708 4235 1584 377 373 235 252 406 299 72 206 Months of occurrence; Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 3 1 I 102 129 155 487 589 2060 2065 224 108 16 Selected annual totals from fixed traps; W. CORNWALL [1] lOS; St Agnes - 614 (Hicks, 2004); lOS; St Mary’s, Longstone - 1488 (Scott, 2004a); The Lizard - 396 at three sites (Tunmore, 2004). DORSET [9] Bridport area - 122 at two sites (Parsons & Brereton, 2004); Portland Bird Observatory - 1737 (Cade, 2004); West Bexington - 768 (Eden, 2004). ISLE OF WIGHT [10] Approximate Island total - 1000 (Knill-Jones, 2004); Totland - 350 (SAK-J). W. SUSSEX [13] Selsey - 157 at two sites (Patton, 2004). E. SUSSEX [14] Elms Farm, Icklesham - 322 (Hunter, 2004). E. KENT [15] Dungeness area - 490+ at thirteen sites (per SPC); Isle of Thanet - 398 at seven sites (Solly, 2004). S. ESSEX [18] Bradwell-on-Sea - 288 (Dewick, 2004). E. SUFFOLK [25] Landguard Bird Observatory - 94 (Odin, 2004). E. NORFOLK [27] Eccles-on-Sea - 158 (Bowman, 2004). CHESHIRE [58] County total - 165 (per SF). S.E. YORKSHIRE [61] Spurn area - 265 at three sites (BRS, PAC). ISLE OF MAN [71] Dhoon Maughold - 114 (per GDC); Knocksharry - 68 (per GDC). WICKLOW [H20] Ashford - 122 (AT). Ealiest dates; W. CORNWALL [1] lOS; St Mary’s, Longstone, 13.1, 14.1, 19.1 (MAS). E. CORNWALL [2] Looe, 24.3 (TS). E. KENT [15] Isle of Thanet, 11.3 (Solly, 2004). GLAMORGAN [41] Porthcawl, 7.3, 8.3 (Gilmore, 2004). SHETLAND ISLANDS [112] Eswick, 21.3 (2), 22.3 (2), 23.3 (5) (TR); Foula, 19.3, 20.3 (2), 23.3 (7) (G. & D. Atherton). Latest dates; W. CORNWALL [1] lOS; St Mary’s, Longstone, 2.12 (Scott, 2004a). N. WILTSHIRE [7] Highworth, 4.12 (SN). DORSET [9] Upwey, 18.12 (PH); Walditch, 2.12 (2) (MSP). E. KENT [15] Dumpton, 6.12 (D. Wrathall); Lydd, 2.12 (KR); Pegwell, 12.12 (FS). S. ESSEX [18] Bradwell-on-Sea, 13.12 (Dewick, 2004). HERTFORDSHIRE [20] Hertford, 1.12 (AW per CWP). CHESHIRE [58] Alsager, 10.12 (M. Dale per SF); Romily, 20.12 (SF). Large single night counts; DORSET [9] Portland Bird Observatory, 7.9 (106) (Cade, 2004). E. SUSSEX [14] Elms Farm, Icklesham, 23.8 (47) (Hunter, 2004). E. KENT [15] Lydd Ranges, 13.8 (80, at sugar) (SPC). S. ESSEX [18] Bradwell-on-Sea, 5.9 (54) (Dewick, 2004). 2119 Peridroma saucia (Hb.) Pearly Underwing [I] Total no. reported; 1688 Distribution of records; SW CS SE EA SI W CE NE NW S I I 542 809 149 44 15 14 2 9 86 1 17 Months of occurrence; Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 2 6 12 58 40 153 430 214 44 10 Selected annual totals from fixed traps; W. CORNWALL [1] lOS; St Agnes - 71 (Hicks, 2004); lOS; St Mary’s, Longstone - 266 (Scott, 2004a); The Lizard - 144 at three sites (Tunmore, 2004). DORSET [9] Portland Bird Observatory - 393 (Cade, 2004); West Bexington - 139 (Eden, 2004). ISLE OF WIGHT [10] Approximate Island total - 200 (Knill-Jones, 2004); Totland - 53 (SAK-J). E. KENT [15] Dungeness area - 49 at twelve sites (per SPC); Isle of Thanet - 70 at seven sites (Solly, 2004). ISLE OF MAN [71] Dhoon Maughold - 77 (per GDC). Ealiest dates; W. CORNWALL [1] lOS; St Mary’s, Longstone, 12.1, 13.1, 14.1 (MAS). E. KENT [15] Isle of Thanet, 9.3 (Solly, 2004). Latest dates; W. CORNWALL [1] lOS; St Mary’s, Longstone, 14.12, 18.12 (3), 24.12 (MAS). WICKLOW [H20] Ashford, 24.12 (AT). 2003 IMMIGRATION REVIEW 33 Large single night counts: W. CORNWALL [1] lOS: St Mary’s, Longstone, 17.9 (8), 13.10 (8) (Scott, 2004a). DORSET [9] Portland Bird Observatory, 1.9 (48) (Cade, 2004). Most northerly records: FLINTSHIRE [51] Hawarden, 9.11 (G. Neal per SN). S.E. YORKSHIRE [61] Haxby, 22.8 (per TE); Kilnsea, 6.11 (PAC); Rudston, 11.6 (perTE); Spurn area, 19.8 - 2.10 (6) (BRS). ISLE OF MAN [71] Dhoon Maughold, 27.8 - 3.10 (77) (per GDC); Minorca Laxey, 3.7, 15.9 (per GDC). SHETLAND ISLANDS [112] Baltasound, 18.9 (anon.). Selected inland records: N. HAMPSHIRE [12] Selborne, 15.6, 16.8, 19.11 (AEA). SURREY [17] Carshalton, 15.9 (D.A. Coleman per GAC); Mayford, 9.8 (M.E.J. Waller per GAC). HERTFORDSHIRE [20] Bishops Stortford, 30.9 (T.J. Lewis per CWP); Harpenden, 28.4, 18.5 (PG per CWP); Hertford, 14.8 (AW per CWP). MIDDLESEX [21] Hampstead, 25.6, 29.6, 4.7, 5.9 (R.A. Softly). BERKSHIRE [22] Slough, 9.9 (R. Hayward). BUCKINGHAMSHIRE [24] Longwick, 12.11 (A. Kershaw per SN). W. SUFFOLK [26] Nowton, undated (RFE per AWP); Sicklesmere, 7.11 (SD per AWP). LEICESTERSHIRE [55] Melton Mowbray, 20.9 (H.J. Orridge per APR). NOTTINGHAMSHIRE [56] Bunny, near Nottingham, 15.7 (M.E. Marchant per SW). S.E. YORKSHIRE [61] Haxby, 22.8 (per TE). 2195 Mythimna vitellina (Hb.) Delicate [I] Total no. reported: 192 Distribution of records: SW cs SE EA SI w CE NE NW S I 97 72 19 2 - 1 - - 1 - - Months of occurrence: Jan Feb Mar Apr May Jun Ju! Aug Sep Oct Nov Dec - - - 2 7 13 15 33 51 35 2 - Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Mary’s, Longstone - 48 (Scott, 2004a); The Lizard - 18 at three sites (Tunmore, 2004). DORSET [9] Portland Bird Observatory - 30 (Cade, 2004); West Bexington - 20 (RE per PAD). Ealiest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 28.4, 29.4, 2.5 (MAS); near Penzance, 4.5 (LO). DORSET [9] Kingcome, 3.5 (N. Spring per PAD). E. KENT [15] Littlestone, 6.5 (KR). Latest dates: DORSET [9] Shapwick, 19.11 (PAD); West Bexington, 17.11 (RE per PAD). Large single night counts: W. CORNWALL [1] Coverack, The Lizard, 13.10 (5) (DCGB); S. DEVON [3] Prawle Point, 20.8 (7) (PF per RFM). DORSET [9] Portland Bird Observatory, 23.8 (5) (Cade, 2004). Most northerly records: ISLE OF MAN [71] Dhoon Maughold, 28.9 (per GDC). Selected inland records: N. DEVON [4] Nr. Hatherleigh, 20.9 (R. Wolton per RFM). 2203 Mythimna unipuncta (Haw.) White-speck [I][MC?] Total no. reported: 4362 Distribution of records: SW CS SE EA SI w CE NE NW S I 2944 1230 51 6 1 51 - 4 36 1 38 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 12 1 2 1 19 71 19 532 894 982 955 238 Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 391 (MEH, AD); lOS: St Mary’s, Longstone - 1975 (Scott, 2004a); The Lizard - 394 at three sites (Tunmore, 2004). DORSET [9] Portland Bird Observatory - 406 (Cade, 2004); Puddletown - 170 (HWH); West Bexington - 228 (RE). Ealiest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 12.1, 13.1 (2) (MAS); The Lizard, 21.3 (Tunmore, 2004). Latest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 28.12 (3), 30.12, 31.12 (MAS). DORSET [9] Portland Bird Observatory, 2.12 (2) (MC); Upwey, 10.12 (PH); Walditch, 1.12 (MSP); West Bexington, 4.12 (RE). W. SUSSEX [13] Walberton, 1.12 (JTR per CRP). 34 ENTOMOLOGIST'S RECORD, VOL. 119 25.i.2007 Large single night counts: W. CORNWALL [1] Coverack, The Lizard, 12.10 (22), 13.10 (25) (DCGB); lOS: St Mary’s, Longstone, 17.11 (130), 18.11 (85), 24.11 (49), 18.12 (67), 24.12 (24) (MAS). DORSET [9] Durlston, 5.9 (20) (DCGB). GLAMORGAN [41] Ty Capel, 14.10 (21) (S&SW). Most northerly records W. LANCASHIRE [60] Bispham, 9.10 (B. Brigden per SMP); Burrow Heights, 1.10 - 27.10 (7) (B. Cockbum per SMP); Heysham, 21.9, 27.10 (J. Holding, P. Marsh per SMP); Lightfoot Green, 8.10, 11.10, 27.10 (SMP); Silverdale, 27.9 (J. Swift per SMP); St Annes, 27.9 (J. Steeden per SMP). S.E. YORKSHIRE [61] Kilnsea, 5.10 (BRS), 18.11 (PAC); Spurn, 19.9 (BRS), 20.11 (BRS per PAC). ISLE OF MAN [71] Island total - 25 (Craine, 2004). SHETLAND ISLANDS [112] Quendale, 16.9 (anon.). Selected inland records: W. SUSSEX [13] Warnham, 21.11 (S. Bayley per CRP). E. SUSSEX [14] Crawley, 15.6 (M. Read per SN); Crawley Down, 16.9 (JHC per CRP). BERKSHIRE [22] Fernham, 1 9. 1 1 (SN). E. NORFOLK [27] Scole, 30.7, 3 1 .7, 1 3.8, 28.8 (M. Hall per DH). 2385 Spodoptera exigua (Hb.) Small Mottled Willow [I] Total no. reported: 5201 Distribution of records: sw 1 cs 1 SE EA j SI 1 W_| CE NE NW S I 1918 2450 629 27 36 37 1 10 1 21 - 72 Months of occurrence: Jan j Feb Mar Apr j May Jun Jul Aug Sep Oct Nov Dec - ! - 4 1 1 1 1 SI 1 915 410 1796 590 107 7 - Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 1023 (Hicks, 2004); lOS: St Mary’s, Longstone - 658 (Scott, 2004a); The Lizard - 149 at three sites (Tunmore, 2004). DORSET [9] Portland Bird Observatory - 856 (Cade, 2004); Puddletown - 360 (HWH); West Bexington - 184 (RE). ISLE OF WIGHT [10] Bonchurch - 80+ (JH); Totland - 97 (SAK-J). W. SUSSEX [13] Kingsham - 314 (Patton, 2004). E. SUSSEX [14] Peacehaven - 112 (Pratt, 2004). E. KENT [15] Dungeness area - 115 at eleven sites (per SPC); Isle of Thanet - 107 at seven sites (Solly, 2004). S. ESSEX [18] Bradwell-on-Sea - 46 (Dewick, 2004). WEXFORD [H12] Tacumshin area, 22- 24.8 (15) (Allen, 2()04).WICKLOW [H20] Ashford - 38 (AT). Ealiest dates: W. CORNWALL [1] lOS: St Agnes, 24.3 (Hicks, 2004); lOS: St Mary’s, early April, by day (W.J. Scott); St Mary’s, Longstone, 24.3 (2), 26.3, 4.4 (MAS); The Lizard, 24.3 (MT). Latest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 6.11, 9.11 (MAS). WICKLOW [H20] Ashford, 6.11 (2) (AT). Large single night counts: W. CORNWALL [1] lOS: St Mary’s, Longstone, 8.8 (32) (Scott, 2004a). DORSET [9] Durlston, 26.6 (47) (PAD, SN), 5.9 (50) (DCGB); Langton Matravers, 5.9 (30) (DCGB); Portland Bird Observatory, 14.6 (109), 15.6 (93) (MC). W. SUSSEX [13] Kingsham, 8.8 (37), 9.8 (35) (SJP per CRP). E. SUSSEX [14] Winchelsea Beach, 8.8 (20) (DCGB). Most northerly records: S. LANCASHIRE [59] Altcar, 8.8 (G. Jones, SMP); Billinge, 22.8 (C. Darbyshire per SMP); Chorlton, 21.9 (B. Smart per SMP); Flixton, 20.7 (K. McGabe per SMP); Hutton, 27.8 (A. Barker per SMP); Parr, 23.8 (2) (R. Banks per SMP). W. LANCASHIRE [60] Aldcliffe, 10.8 (P. Marsh per SMP); Heysham, 17.6 (J. Holding per SMP). S.E. YORKSHIRE [61] Kilnsea, 16.9 (BRS). ISLE OF MAN [71] Dhoon Maughold, 11.7 - 3.10 (9) (Craine, 2004); Minorca Laxey, 7.8, 26.8 (per GDC). Selected inland records: N. HAMPSHIRE [12] Selborne, 5.7, 11.8 (2), 12.8 (3), 13.8 (2) (AEA); Sherborne St John, 2.8 (N. Montegriffo). SURREY [17] Ockley, 16.8 (W. Attridge per GAC); West Molesey, 23.6 (PR. Williams per GAC); Weybridge, 23.8 (A.R. Mitchell per GAC). S. ESSEX [18] Epping, 21.7 (T. Green per BG). HERTFORDSHIRE [20] Bishops Stortford, 12.8 (CWP), 18.9 (JF per CWP); Broxbourne Wood, 4.8 (CWP); Marshalls Heath, 26.6 (J. Murray per SN); Millhoppers Pasture, 23.8 (CWP); Ravensdell Wood, 9.8 (CWP). BERKSHIRE [22] Dry Sandford, 5.8, 21.9 (AK); Fernham, 22.6, 18.7, 6.8 (2) (SN); Slough, 22.8 (R. Hayward). W. NORFOLK [28] South Lopham, 9.8 (LB-L per DH). CAMBRIDGESHIRE [29] Wicken, 10.8 (DEW). BEDFORDSHIRE [30] Flitwick Moor, 22.8 (C.R.B. Baker per LH); Maulden Woods, 6.8 (CWP per LH). WORCESTERSHIRE [37] Crossway Green, 26.6 (M. Southall per SN). WARWICKSHIRE [38] Bidford-on-Avon, 12.8 (R.M. Cox per DCGB); Charlecote, 30.6 (A.F. Gardner per DCGB), 17.8, 18.8 (DCGB). LEICESTERSHIRE [55] Dadlington, 31.5 (R. Smith per APR). DERBYSHIRE [57] Ault Hucknall, 5.9 (Budworth et al, 2004); Melbourne, 22.8, 24.8 (Budworth et al, 2004); Whitwel! Wood, 23.8 (Budworth et al, 2004). S. LANCASHIRE [59] Chorlton, 21.9 (B. Smart per SMP); Flixton, 20.7 (K. McGabe per SMP). 2003 IMMIGRATION REVIEW 35 2400 Helicoverpa armigera (Hb.) Scarce Bordered Straw [I][In] Total no. reported: 1030 Distribution of records: sw cs SE EA SI W CE NE NW S I 340 456 177 15 9 6 4 6 8 1 8 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec - - - - - 21 21 206 285 177 13 - Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Agnes - 60 (MEH, AD); lOS: St Mary’s, Longstone - 148 (Scott, 2004a); The Lizard - 59 at three sites (Tunmore, 2004). DORSET [9] Portland Bird Observatory - 84 (Cade, 2004); Puddletown - 51 (HWH); West Bexington - 69 (Eden, 2004). ISLE OF WIGHT [10] Approximate Island total - 100 (Knill-Jones, 2004); Bonchurch - 30+ (JH); Totland - 14 (SAK-J). W. SUSSEX [13] Selsey - 20 at two sites (Patton, 2004). E. SUSSEX [14] Peacehaven - 22 (CRP). E. KENT [15] Dungeness area - 39 at eleven sites (per SPC); Isle of Thanet - 87 at seven sites (Solly, 2004). S. ESSEX [18] Bradwell-on-Sea - 16 (Dewick, 2004). Ealiest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 18.6, 24.6, 25.6, 26.6 (2) (MAS). N. DEVON [4] Hartland Point, 22.6 (BPH, REM). DORSET [9] Durlston, 26.6 (2) (PAD, SN); Wool, 23.6 (D. Cooper). ISLE OF WIGHT [10] Bonchurch, 26.6 (JH). E. SUSSEX [14] Peacehaven, 26.6 (2) (CRP). Latest dates: S. DEVON [3] Chardstock, 15.11 (A. Jenkins per RFM). DORSET [9] Portland Bird Observatory, 9.11 (Cade, 2004); Upwey, 9.11, 10.11 (PH). W. SUSSEX [13] Walberton, 14.11 (JTR per CRP). E. KENT [15] Isle of Thanet, 19.11 (Solly, 2004). Large single night counts: W. CORNWALL [1] Coverack, The Lizard, 12.10 (7), 13.10 (20), 15.10 (6) (DCGB); lOS: St Agnes, 12.10 (7), 14.10 (5), 15.10 (6) (Davison, 2004); lOS: St Mary’s, Longstone, 25.9 (11) (Scott, 2004a). DORSET [9] Durlston, 5.9 (12) (DCGB). ISLE OF WIGHT [10] Bonchurch, 30.8 (5) (JH); Compton Bay, 16.8 (15+) (A. Kolaj, in Collins, 2004). W. SUSSEX [13] Pagham, 20.9 (4) (JHC, THE per CRP). Most northerly records: MERIONETHSHIRE [48] Maentwrog, 22.8 (2) (DCGB). CHESHIRE [58] Allostock, 19.8 (P.M. Hill per SF); Great Sutton, 1.10 (M. Bellingham per SF). S. LANCASHIRE [59] Orrell, 4.9 (P. Alker per SMP). W. LANCASHIRE [60] Heysham, 8.8 (J. Holding per SMP). S.E. YORKSHIRE [61] Bishop Burton, 18.9, 20.9 (per TE); Kilnsea, 18.9 (PAC), 23.9, 3.10 (BRS); Spurn, 27.9, by day (BRS). S.W. YORKSHIRE [63] Bellflask, near Ripon, 17.9 (per TE); Rawmarsh, near Rotherham, 12.7 (D. Stables per SN). N.W. YORKSHIRE [65] Hutton Conyers, 30.9 (per TE). ISLE OF MAN [71] Dhoon Maughold, 18.9, 20.9 (per GDC); Orrisdale 28.8 (per GDC). SHETLAND ISLANDS [112] Burrafirth, 12.8 (anon.). Selected inland records: N. WILTSHIRE [9] Avebury, 27.9 (Collins, 2004). N. HAMPSHIRE [12] Cholderton, 24.8 (H. Edmunds per TN); Grateley, 17.8 (S. Colenutt per TN). HERTFORDSHIRE [20] Bishops Stortford, 6.8 (JF per CWP); Hitchin, July, undated (K. Robinson per CWP). BERKSHIRE [22] Dry Sandford, 7.9, 27.9 (AK). W. SUFFOLK [26] Nowton, undated (REE per AWP). CAMBRIDGESHIRE [29] Wicken, 9.9 (DEW). WARWICKSHIRE [38] Charlecote, 21.8 (DCGB); Rugby, 20.9 (I.G.M. Reid per DCGB). S.W. YORKSHIRE [63] Bellflask, near Ripon, 17.9 (per TE); Rawmarsh, near Rotherham, 12.7 (D. Stables per SN). N.W. YORKSHIRE [65] Hutton Conyers, 30.9 (per TE). Immature stages: W. CORNWALL [1] Lizard Point, 20.10, larva on Lavatera arborea (adult reared 9.6.04) (J. Nelson, MT). 2403 Heliothis peltigera (D. & S.) Bordered Straw [I] Total no. adults reported: 1241 Distribution of records: SW CS SE EA SI W CE NE NW S I 257 606 229 34 37 19 30 7 7 - 15 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec - - 1 1 3 399 143 322 88 3 - - 36 ENTOMOLOGIST'S RECORD, VOL. 119 25.i.2007 Selected annual totals from fixed traps: W. CORNWALL [1] lOS; St Agnes - 30 (Hicks, 2004); lOS: St Mary’s, Longstone - 113 (Scott, 2004a); The Lizard - 19 at three sites (Tunmore, 2004). DORSET [9] Portland Bird Observatory - 86 (Cade, 2004); Puddletown - 30 (HWH); West Bexington - 120 (Eden, 2004). ISLE OF WIGHT [10] Bonchurch - 60+ (JH); Totland - 10 (SAK-J). W. SUSSEX [13] Kingsham - 27 (Patton, 2004). E. SUSSEX [14] Peacehaven - 18 (CRP). E. KENT [15] Dungeness area - 80 at twelve sites (per SPC); Isle of Thanet - 50 at seven sites (Solly, 2004). E. SUFFOLK [25] Landguard Bird Observatory - 13 (Odin, 2004). WICKLOW [H20] Ashford - 9 (AT). Ealiest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 6.4 (Scott, 2004a). E. NORFOLK [27] Weybourne, 24.3 (MP per DH). Latest dates: W. CORNWALL [1] lOS: St Mary’s, Longstone, 28.10 (Scott, 2004a). DORSET [9] Preston, 11.10 (MF). E. KENT [15] Lydd-on-Sea, 3.10 (KA). Large single night counts: W. CORNWALL [1] lOS: St Mary’s, Longstone, 14.6 (9), 16.6 (15), 26.6 (10) , 30.6 (9) (MAS). DORSET [9] Durlston, 25.6 (8) (JMc), 26.6 (43) (PAD, SN), 5.9 (6) (DCGB); Portland Bird Observatory, 4.7 (6) (MC); West Bexington, 10.8 (12) (RE). ISLE OF WIGHT [10] Bonchurch, 23.6 (5), 7.8 (6) (JH). Large diurnal counts; W. CORNWALL [1] lOS: St Mary’s, Longstone, 16.6 - 7.7 (41), including 12 on 16.6 (Scott, 2004a). S. DEVON [3] Torquay, 6.7 (7) (W. Deakins per RFM). Most northerly records: S. LANCASHIRE [59] Hutton, 5.7 (A. Barker per SMP); Hawick, 16.8 (A. Barker per SMP). W. LANCASHIRE [60] Heysham, 17.6 (J. Holding per SMP); Yealand Conyers, 17.9 (B. Hancock per SMP). S.E. YORKSHIRE [61] Easington, 22.8 (M.J. Stoyle per BRS); Kilnsea, 2.7 (PAC); Spurn, 10.8 (2), 23.8, 7.9, the last by day (BRS). N.E. YORKSHIRE [62] Saltbum-by-the-Sea, 17.9 (per TE). N.W. YORKSHIRE [65] Hutton Conyers, 14.9 (per TE). ISLE OF MAN [71] Dhoon Maughold, 20.9 (per GDC); Orrisdale, 18.8 (per GDC). WICKLOW [H20] Nr. Newcastle, 9.8 (Jeffares, 2003). Selected inland records: N. WILTSHIRE [7] Highworth, 30.6, 6.7 (SN). S. WILTSHIRE [8] Tilshead, 27.6 (2), by day (JMc). N. HAMPSHIRE [12] Basingstoke, 2.6 (MW); Grateley, 3.6, 7.8, 9.8 (S. Colenutt per TN); Greywell, 13.6 (Collins, 2004); Magdalen Hill Down, 20.8 (P. Fleet per TN); South Wonston, 26.6 (P.J.S. Smith per TN). SURREY [17] Capel, near Dorking, 9.6 (D. Fraser); Epsom Downs, 18.9 (B.J. Grabaskey per GAC). HERTFORDSHIRE [20] Bishops Stortford, 18.8 (AH per CWP), 21.8 (JF per CWP); Harpenden, 17.6 (PG per CWP); Hertford, 26.6 (AW); Millhoppers Pasture, 23.8 (CWP); Royston, 5.8, 17.8, 26.8 (JEC per CWP); Ware, 18.8 (EG per CWP); Weston, 28.9 (A. Cockburn per CWP). BERKSHIRE [22] Dry Sandford, 26.6 (AK); Femham, 22.6, 2.7, 6.8 (SN). W. SUFFOLK [26] Great Comard, 5.9, 19.9 (SR per AWP); Hopton, 7.9 (PB^ per AWP). E. NORFOLK [27] Scole, 7.8 (M. Hall per DH). HUNTINGDONSHIRE [31] Yaxley, June (undated), 28.6 (by day) (A. Frost per BD). NORTHAMPTONSHIRE [32] Werrington, 26.9 (P. Waring). WORCESTERSHIRE [37] Crossway Green, 19.6, 10.7, 11.7 (M. Southall per SN); Malvern, 6.7 (D.B. Throup per SN). WARWICKSHIRE [38] Charlecote, 17-29.6 (3), 3.7, 1.8, 17.8, 14.9, 30.9 (DCGB). LEICESTERSHIRE [55] Barrowden, 12.8 (R. Eollows per APR); Braunstone, 17.8, 5.9 (L. Holton per APR); Penny Drayton, undated (H.N. Ball per APR); Loughborough, 5.9 (N.J. Campsall per APR); Luffenham Heath, 18.7 (R. Follows per APR); Markfield, 26.8 (AJM per APR). NOTTINGHAMSHIRE [56] Newark-on- Trent, 4.8 (DA); Sutton-on-Trent, 4.8 (MK). DERBYSHIRE [57] Buxton, 31.7 (2) (S.A. Orridge per SHH); Swadlincote, 27.6 (Budworth et al, 2004). CHESHIRE [58] Alsager, 5.9, 14.9 (M. Dale per SF); Altrincham, 14.6 (R. Hilton per SF); Nantwich, 11.7 (D. Taylor per SF); Romily, 11.6 (SF). N.W. YORKSHIRE [65] Hutton Conyers, 14.9 (per TE). Immature stages: Pagham Harbour, 30.7, ‘hundreds of larvae’ (SJP). 2441 Autographa gamma (L.) Silver Y [I] Total no. adults reported (light-trap records only): 74768 Distribution of records; sw CS SE EA SI W CE NE NW S I 5175 32819 14321 8547 4082 973 2755 3030 755 435 1876 Months of occurrence: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 2 1 5 83 224 3305 8005 22115 3294 481 157 22 Selected annual totals from fixed traps: W. CORNWALL [1] lOS: St Mary’s, Longstone - 1837 (Scott, 2004a); The Lizard - 1441 at three sites (Tunmore, 2004). DORSET [9] Bridport area - 1000 at two sites (Parsons & Brereton, 2004); Portland Bird Observatory - 9563 (Cade, 2004); West Bexington 2003 IMMIGRATION REVIEW 37 - 8531 (Eden, 2004). ISLE OF WIGHT [10] Approximate Island total - 7000 (Knill-Jones, 2004); Totland - 2200 (SAK-J). W. SUSSEX [13] Selsey - 2142 at two sites (Patton, 2004). E. SUSSEX [14] Peacehaven - 2058 (Pratt, 2004). E. KENT [15] Isle of Thanet - 2894 at seven sites (Solly, 2004); Kingsdown - 1211 (Jarman, 2004). S. ESSEX [18] Bradwell-on-Sea - 4737 (Dewick, 2004). E. NORFOLK [27] Eccles-on-Sea - 2926 (Bowman, 2004). S.E. YORKSHIRE [61] Kilnsea - 1870 (PAC). WEXFORD [H12] Tacumshin area, 22-24.8 (432) (Allen, 2004). WICKLOW [H20] Ashford - 1016 (AT). Ealiest dates; W. CORNWALL [1] lOS: St Mary’s, Longstone, 1.1, 2.1 (MAS); The Lizard, 31.3 (Tunmore, 2004). DORSET [9] Dorchester, 29.3 (J. Down); Preston, 23.2 (RL). E. KENT [15] Isle of Thanet, 11.3 (Solly, 2004). GLAMORGAN [41] Porthcawl, 21.3 (Gilmore, 2004). Latest dates; W. CORNWALL [1] lOS; St Mary’s, Longstone, 24.12 (Scott, 2004a); Mylor Churchtown, 19.12 (Cooke, 2004). S. DEVON [3] Starcross, 15/21.12 (Rothamsted Trap) (AHD). DORSET [9] Durlston Country Park, 22.12 (2) (SN). S. HAMPSHIRE [11] Portchester, 22.12 (IS). SURREY [17] New Haw, 17.12 (P.R. Wheeler per GAC). Large single night counts; DORSET [9] Durlston, 26.6 (150) (PAD, SN), 5.8 (132), 7.8 (640) (JMc); Portland Bird Observatory, 11.8 (1558) (Cade, 2004); Southwell, Portland, 6.8 (500) (JHC). S. HAMPSHIRE [11] Portchester, 7.8 (134) (IS). E. KENT [15] Dungeness Bird Observatory, 11.8 (153) (DW); Kingsgate, 6.8 (214) (FS). S. ESSEX [18] Bradwell-on-Sea, 6.8 (803) (Dewick, 2004). E. SUFFOLK [25] Landguard Bird Observatory, 6.8 (656) (Odin, 2004). E. NORFOLK [27] Eccles-on- Sea, 21.7 (287) (Bowman, 2004). BEDFORDSHIRE [30] Nr. Milton Keynes, 1.7 (135) (LH). WICKLOW [H20] Ashford, 21.8 (195), 17.9 (219) (AT). Large diurnal/dusk counts; W. CORNWALL [1] lOS; St Mary’s, Longstone, 3.7 (300) (MAS). DORSET [9] Durlston, 25.6 (500) (PAD); Studland, 27.8 (500) (PAD). N. ESSEX [19] Jaywick, 14.8 (1200) (JY per BG). E. SUFFOLK [25] Landguard Bird Observatory, 7.8 (300+) (NO per AWP). E. NORFOLK [27] Nr. Hockwold, 2.8 (15,000), in a Lucerne field (P. Laurie). PEMBROKESHIRE [45] Skomer Island, annual total; 38946; August total; 37356 (including 10000+ on 25.8) (Hayden, 2004). LINCOLNSHIRE [54] Gibraltar Point, 27.7 (150) (Sykes, 2004). S.E. YORKSHIRE [61] Spurn Point, 5.7 (500), 16.7 (1200), 2.8 (6000) (BRS). W. CORK [H3] Dursey Island, 13.7 (500+) (Scott, 2004b). Immature stages; W. CORNWALL [1] Paul, 20.7, many larvae on cut calabrese (J. Worth). S. DEVON [3] Torquay, 13.8, two larvae on Parietaria judaica. E. KENT [15] Nr. Canterbury, undated, three larvae on Ocimum basilicum in a supermarket (S. Warry per IDF). LEICESTERSHIRE [55] Broughton Astley, 16.8, two larvae on Geranium (G. Adams per APR). ANNEX SELECTED 2003 CHANNEL ISLANDS [VC 113] RECORDS 1384 Phlyctaenia stachydalis (Germar) Guernsey; L’Ancresse, 12.7 (RA); St Martins, 10.7 (RA); first VC records. 1448a Elegiafallax (Stdgr.) Guernsey; St Peters, 16.4, first VC record (Sterling & Costen, 2005). 1539 Papilio machaon ssp. gorganus (Fruhs.) Continental Swallowtail Guernsey; Bordeaux Tip, 28.7 (M. Bougourd per RA), Pecqueries, 21.7 (I. Hall per RA). 1567 Lampides boeticus (L.) Long-tailed Blue Guernsey; Jaonnet Bay, 15.10 (A. Smith per RA); St Peter Port, 15.9 (not 3.9 as stated in Austin, 2004a) (J. Gilmore, in Austin, 2004b). Jersey; Grouville, 7.8 (3), 8.8 (2), then 35+ across the island during the rest of August (DJW, in Jones, 2004). 1594 Agiais polychloros (L.) Large Tortoiseshell Herm; 21.3 (B. Kendall per RA). 1639 Dendrolimus pini (L.) Pine-tree Lappet Guernsey; Icart, 31.7 (TNDP). 1678a Cyclophora ruficiliaria (H.-S.) Jersey Mocha Guernsey; Icart, 18.7, first Guernsey record (TNDP per RA). 1684 Scapula nigropunctata (Hufn.) Sub-angled Wave Jersey; Trinity, 2.7, first VC record (RIS, in Gould, 2005). 1973 Acherontia atropos (L.) Death’s-head Hawk-moth Guernsey; St Martins, 20.10 (Austin, 2004a); St Peter Port, 18.9 (PC). 2018 Clostera anachoreta (D. & S.) Scarce Chocolate-tip Guernsey; L’Ancresse, 1.8, first Guernsey record (RA). 38 ENTOMOLOGIST’S RECORD, VOL. 119 25.i.2007 2083 Euxoa cursoria (Hufn.) Coast Dart Herm: 28-30.7, first VC record (DJW per RA). 2160a Lacanobia splendens (Hb.) I^lendid Brocade Jersey: Surville, 21.6 (2) (RLO; Guernsey: Icart, 17.7 (Austin, 2004b); St Peters Port, 5.7 (PC). 2223 Calophasia lunula (Hufn.) Toadflax Brocade Guernsey: St Peter Port, 22.7, first VC record (Austin, 2004a). 2387a Platyperigea kadenii (Frey.) Clancy’s Rustic Guernsey: Icart, 17.9, 5.10 (not 15.9 & 2.10 as given in Austin, 2004a) (TNDP, in Collins, 2004); St Peters Port, 19.9 (PC). Jersey: Grouville, 18.9 (R. Hayward). The first VC records. 2404 Heliothis nubigera (H.-S.) Eastern Bordered Straw Guernsey: St Peter Port, 30.8 (D. Andrews per RA); L’Ancresse, 6.9 (2) (RA); St John, 16.8 (RA); St Martins, 25.6 (RA); first VC records. 2436 Macdunnoughia confusa (Steph.) Dewick’s Piusia Guernsey: Icart, 5.9 (TNDP per RA). 2451 Catocala fraxini (L.) Clifden Nonpareil Guernsey: St Peters Port, 12.10 (PC). 2453 Catocala electa (View.) Rosy Underwing Guernsey: Forest, 18.8 (TNDP per RA); Mont D’Aval, 21.8 (M. Simmons per RA); St Johns, 5.8 (RA). Jersey: Grouville, 7.8 (2), 8.8 (2) (DJW, in Collins, 2004), 17.9 (R. Hayward, in Collins, 2004). These records are likely to be associated with a breeding population in VC 113. APPENDIX 1 Corrections/Additions to 2002 report 0897b Anatrachyntis simplex (Wals.) [In] S. DEVON [3] Nr. Ivybridge, moth bred on 29.1 from a larva found in a pomegranate purchased from a supermarket on 22.12.01, stated to have been imported from India. New to Britain (RJH, in Beaumont, 2004). 1389 Udeafulvalis (Hb.) [I][MC] S. HAMPSHIRE [11] Ringwood, 22.7 - 13.8 (13) (RE); likely to be the result of local colonisation. 2403 Heliothis peltigera (D. & S.) Bordered Straw [I] CAMBRIDGESHIRE [29] Wicken, 31.8, 11.9 (DEW). 2432 Trichoplusia ni (Hb.) Ni Moth [I] CAMBRIDGESHIRE [29] Wicken, 14.8 (DEW). Correction to 1998 report 2411 Deltote deceptoria (Scop.) Pretty Marbled [I] [E. KENT [15] Greatstone, 20.6 (BB) (Ent Rec. 112: 246). Erroneous record.] Initials of recorders AC Cornish, A. GMH Haggett, G.M. NMH Hall, N.M. AD Davison, A. HWH Wood Homer, H. NO Odin, N. AEA Aston, A.E. IC Cook, I. NW Whinney, N. AGJB Butcher, A.G.J. IDF Ferguson, I.D. OD Davis, O. AH Hardacre, A. IDH Hunter, I.D. PAD Davey, PA. AHD Dobson, A.H. IM Mathieson, I. PAC Crowther, P.A. AJB Bradshaw, A.J. IR Rippey, I. PB Bergdahl, P. AJM Mackay, A.J. IRT Thirlwell, I.R. Pb2 Bryant, P. AJP Pickles, A.J. JA Astley, J. PC Costen, P. AK Kennard, A. JBH Higgott, J.B. PF Franghiadi, P. AM Musgrove, A. JBW Webb, J.B. PH Harris, P. AMD Davis, A.M. JC Clifton, J. phb Boggis, PH. ANG Graham, A.N. & J.E. JE Ellis, J. PHS Stirling, P.H. 2003 IMMIGRATION REVIEW 39 APR Russell, A.P. JEC Chainey, J.E. PK Kitchener, P. ARC Collins, A.R. JH Halsey, J. RA Austin, R. ASH Henderson, A.S. Jh2 Herbert, J. RC Clamp, R. AT Tyner, A. JHC Clarke, J.H. Rc2 Cox, R. AW Wood, A. JMc McGill, J. RDP Penhallurick, R.D. Aw2 Wander, A. JO Owen, J. RE Eden, R. AWP Pritchard, A.W. JRL Langmaid, J.R. REL Lane, R.E. BB Banson, B. IS Stokes, J. RF Fox, R. BD Dickerson, B. JTR Radford, J.T. RFE Eley, R.E BPS Skinner, B.F. JW Waddell, J. RFM McCormick, R.F. BG Goodey, B. JY Young, J. RH Hollins, R. BKW West, B.K. KA Arter, K. RIS Rothamsted Insect Survey B&LB Bewsher, B. & L. KB Bond, K. RJH Heckford, R.J. BPH Henwood, B.P. KNAA Alexander, K.N.A. RJM Moore, R.J. BRS Spence, B.R. KR Redshaw, K. RL Lambert, R. BS Stewart, B. Kr2 Regan, K. Rl2 Leverton, R. CH Hart, C. KRT Tuck, K.R. Rl3 Long, R. CG Gibson, C. LB-L Broom-Lynne, L. RM Marsh, R. CM Manley, C. LH Hill, L. RP Parker, R. CR Roots, C. LK Kneale, L. RRC Cook, R.R. CRP Pratt, C.R. MAS Scott, M.A. & WJ. s&sw Walmsley, S. & S. cs Slater, C. MB Bailey, M. SAK-J Knill-Jones, S.A. CT Turley, C. MC Cade, M. SD Dumican, S. CWP Plant, C.W. MC2 Cornish, M. SF Farrell, S. DA Atkinson, D. MCP Perry, M.C. SH Hatch, S. DB Burrows, D. md Deans, M SHH Hind, S.H. DBW Wooldridge, D. ME Easterbrook, M. SHP Piotrowski, S.H. DCGB Brown, D.C.G. MEH Hicks, M.E. SJP Patton, S.J. DEW Wilson, D.E. MF Forster, M. SMP Palmer, S.M. DF Foot, D. MJ Jeffes, M. SN Nash, S. DH Hipperson, D. MK Kennewell, M. SPC Clancy, S.P. Dh2 Hoare, D. MM Marsh, M. SR Read, S. DJW Wedd, D.J. MO’S O’Sullivan, M. SRD Davey, S.R. DRML Long, D.R.M. MP Preston, M. sw Wright, S. DRWG Gilmore, D.R.W. MPS Skevington, M.P. TE Ezard, T. DW Walker, D. MRH Honey, M.R. THF Freed, T.H. FS Solly, F. MSP Parsons, M.S. TN Norriss, T. GAC Collins, G.A. MT Tunmore, M. TNDP Peet, T.N.D. GB Bailey, G. MW Wall, M. TR Rogers, T. GBH Hocking, G.B. NAC Croton, N.A. TS Steele, T. GD Davis, G. NB Bowles, N. VS Shenston, V. GDC Craine, G.D. NG-D Greatorex-Davies, N. VT Tucker, V. NJ Jarman, N. Acknowledgements We would like to thank all of the above mentioned recorders and contributors, in particular those who took the time to send records directly to the authors. It is possible that we have unwittingly failed to acknowledge some contributors, if this is the case we would like to take this opportunity to apologise for this oversight. We are also grateful to the Meteorological Office for facilitating access to, and allowing the publication of, the weather charts included in the introduction. References Allen, D. & Mellon, C., 2004. Moth immigration in south-west Cork, Republic of Ireland. Atropos 22: 56. — , 2004. Immigrant records from southern Co. Wexford, Republic of Ireland. Atropos 22: 63. 40 ENTOMOLOGIST'S RECORD, VOL. 119 254.2007 — , 2004. Addenda et Corrigenda. Entomologist’s Record & Journal of Variation, 116; 280. — , 2005. Insect archive 2003. Website: www.nature-shetland.co.uk. Austin, R., 2004a. Reports from coastal stations - 2003. Guernsey, Channel Islands. Atropos 21: 37-39. — , 2004b. Entomology Section Report for 2003. Report and Transactions o/ La Societe Guemesiaise Volume XXV Part 111: 426-436. Beaumont, H. E., 2004. B.E.N.H.S. 2003 Annual Exhibition: British Microlepidoptera. British Journal of Entomology and Natural History 17, Part 3: 155-161. Boggis, R, 2003. Assistant county recorder’s report. Cornwall Moth Group. Newsletter 3; 1-3. Bowman, N., 2004. Reports from coastal stations - 2003. Eccles-on-Sea, Norfolk. Atropos 21: 65- 66. Budworth, D., Viles, 1. & Wright, S., 2004. Annual Lepidoptera Report 2003, Part 2; Macro Moths. The Derbyshire & Nottinghamshire Entomological Society Journal 153: 8-23. Cade, M., 2004. Reports from coastal stations - 2003. Portland, Dorset. Atropos 21: 47-50. Cade, M., 2004b. Splendid Brocade Lacanobia splendens (Hb.) - the first British records. Atropos 22: 42-44. Chainey, J. & Spence, J., 2004. Jersey Mocha Cyclophora ruficiliaria (H.-S.) - a geometrid moth new to the British Isles. Atropos 23: 13-15. Clancy, S. P, 2004. Reports from coastal stations - 2003. Dungeness area, Kent. Atropos 21: 55- 57. Coker, K. J., 2004. Convolvulus Hawk-moth Agrius convolvuli (L.) (Lep.: Sphingidae) in Hampshire. Entomologist’s Record & Journal of Variation 116: 90. Collins, G. A., 2004. B.E.N.H.S. 2003 Annual Exhibition: British Macrolepidoptera. British Journal of Entomology and Natural History 17, Part 3: 150-155. Cooke, J., 2004. Highlights of 2003. Cornwall Moth Group. Newsletter 4: 3-4. Craine, G. D., 2004. Reports from coastal stations - 2003. Isle of Man. Atropos 21: 68. Davey, P.A., 2004. Macrolepidoptera Report 2003. Dorset Moth Group Newsletter 11: 6-21. Davison, A., 2004. Isles of Scilly Moths 2003 (species table). Website: WWW. simply birdsandmoths. co. uk. Dewick, S., 2004. Reports from coastal stations - 2003. Curry Farm, Bradwell-on-Sea, Essex. Atropos 21: 60-63. Easterbrook, M., 2004. Annual Butterfly Report (Kent) - 2003. Butterfly Conservation (Kent Branch). Eden, R., 2004. Reports from coastal stations - 2003. West Bexington, Dorset. Atropos 21: 45-46. Ferguson, I.D., 2005. Kent Moth Report - 2003. Butterfly Conservation, Kent Branch. Gilmore, D., 2004. Glamorgan Moth Report 2003. Glamorgan Moth Recording Group Newsletter 74: 2-12. Gould, P.J.L., 2005. The Sub-angled Wave Scopula nigropunctata Hufn. (Lep.: Geometridae): A first for the Channel Islands. Entomologist’s Record & Journal of Variation 117; 148. Gregory, J., 2004 notes for 2003. Cornwall Moth Group. Newsletter 4: 6-9. Harmer, A. S., 2004. Macdunnoughia confusa (Steph.) (Lep.: Noctuidae) in Hampshire. Entomologist’s Record & Journal of Variation 116: 77. Harvey, R., 2004. Reports from coastal stations - 2003. Minsmere RSPB Reserve, Suffolk. Atropos 21: 64-65. Hayden, J., 2004. Reports from coastal stations - 2003. Skomer Island, Pembrokeshire. Atropos 21; 68-69. Hicks, M., 2004. Reports from coastal stations - 2003. St Agnes, Isles of Scilly. Atropos 21: 42-43. Hipperson, D., 2003. Records of migrant moths recorded during 2003. Norfolk Moth Survey. Newsletter 6^: 13-15. 2003 IMMIGRATION REVIEW 41 — , 2003. Additional records of migrant moths recorded during 2003. Norfolk Moth Survey. Newsletter 65: 5-6. Hunter, I., 2004. Reports from coastal stations - 2003. Elms Farm, Icklesham, East Sussex. Atropos 21: 54-55. Jarman, N., 2004. Reports from coastal stations - 2003. Kingsdown Beach, Kent. Atropos 21: 59-60. Jeffares, M., 2003. Heliothis peltigera (D. & S.) in Co. Wicklow, Ireland. Entomologist’s Gazette 54: 222. Jobe, J.B. & Fletcher, C., 2004. Antichloris viridis in North Yorkshire. Atropos 23: 60-61. Jones, A. M., 2004. B.E.N.H.S. 2003 Annual Exhibition: British Butterflies. British Journal of Entomology and Natural History 17, Part 3: 147-150. Knill-Jones, S., 2004. Reports from coastal stations - 2003. Isle of Wight. Atropos 21: 50-51. Koryszko, J., 2003. Queen of Spain Fritillary Issoria lathonia (L.) (Lep.: Nymphalidae) in Staffordshire. Entomologist’s Record & Journal of Variation 115: 284. — , 2004. Further records of the Queen of Spain Fritillary Issoria lathonia (L.) (Lep.: Nymphalidae) in Britain during 2003. Entomologist’s Record & Journal of Variation 116: 228. Langmaid, J.R. & Young, M. R., 2004. Microlepidoptera Review of 2003. Entomologist’s Record & Journal of Variation 116: 193-214. Lewis, T., 2004. Some moths in north Pembrokeshire, Wales, during 2003. Entomologist’s Record & Journal of Variation 116: 115-117. Nash, S., 2004. Archived 2003 records (by species). Website: www.migrantmoth.com. — , 2003. Earias vittella (Fabricius) (Lep.: Noctuidae) the first occurrence of wild-caught moths in Europe. Entomologist’s Record & Journal of Variation 115: 187-188. Odin, N., 2004. Reports from coastal stations - 2003. Landguard Bird Observatory, Suffolk. Atropos 21: 63-64. Ofield, B., 2004. Mating Red Admirals Vanessa atalanta. Atropos 21: 81-82. Parsons, M.S. & Brereton, T., 2004. Reports from coastal stations - 2003. Bridport area, Dorset. Atropos 21: 45-46. Patton, S., 2004. Reports from coastal stations - 2003. Selsey, West Sussex. Atropos 21: 51-52. Phillips, J., 2004. Reports from coastal stations - 2003. Hayling Island, Hampshire. Atropos 21: 51. Powell, M. (Ed.), 2003. Recent Reports - October & November 2003 (Migrants). Glamorgan Moth Recording Group Newsletter 73: 5-6. Pratt, C.R., 2004. Reports from coastal stations - 2003. Peacehaven, East Sussex. Atropos 21: 52-53. Scott, M.A. & W.J., 2004a. Reports from coastal stations - 2003. Longstone Heritage Centre, St Mary’s, Isles of Scilly. Atropos 21: 39-42. Scott, D.A., 2004b. Reports from coastal stations - 2003. Dursey Island, Co. Cork. Atropos 21: 69-70. Solly, R, 2004. Reports from coastal stations - 2003. Isle of Thanet. Atropos 21; 57-59. Spence, B.R., 2004. Reports from coastal stations - 2003. Spurn area, East Yorkshire. Atropos 21: 66-68. Sterling, P.H., 2004. Microlepidoptera Report 2003. Dorset Moth Group Newsletter 11: 22-26. Sterling, P.H. & Ashby, M., 2006. Dichelia histrionana (Frolich, 1828) (Lep: Tortricidae) New to the British Isles. Entomologist’s Record & Journal of Variation 118: 19-22. Sterling, P.H. & Costen, P.D.M., 2005. Elegia fallax (Staudinger, 1881) (Lepidoptera: Pyralidae) new to the Channel Islands. Entomologist’s Gazette 56: 75-79. Sykes, T., 2004. Reports from coastal stations - 2003. Gibraltar Point, Lincolnshire. Atropos 21: 66. Tunmore, M., 2004. Reports from coastal stations - 2003. Lizard Peninsula, Cornwall. Atropos 21: 43-45. West, B. K., 2004. Tree Lichen Beauty Cryphia algae (Fabr.) (Lep.: Noctuidae), breeding in Britain. Entomologist’s Record & Journal of Variation 116: 259. Yates, B., 2004. Reports from coastal stations - 2003. Rye Harbour, East Sussex. Atropos 21: 53-54. 42 ENTOMOLOGIST'S RECORD, VOL. 119 25.i.2007 Hazards of butterfy collecting. It seemed a good idea at the time: London 2001 I had arrived in London after more than two months in Ghana where I had been doing an analytical survey of the butterflies in two of Ghana's most important national parks, Ankasa and Bia. The trip had been quite successful and a number of butterflies needed closer investigation, including a couple of suspects for the status of species new to science. When unpacking the butterflies, I discovered to my dismay that the first box opened was under attack by pests - the grey powder inside their semi-transparent paper triangles was unmistakable. I am always very careful to dose each of the storage boxes with naphthalene or paradichlorbenzole. These toxic substances are no longer available commercially in our well-regulated European Union so I buy my supplies locally. However, the shopping around Bia and Ankasa did not stretch far enough to supply “camphor” so some boxes had not been topped up. What to do? Once established, pests are notoriously difficult to eradicate. I had a bright idea. What about zapping them in the microwave? Even eggs could hardly survive a good five minutes at full blast. I made a selection of butterflies of various sizes and hues for a test, put them on a plate . . . and even remembered to add a glass of water for the benefit of the microwave. After five minutes the butterflies looked none the worse for wear. Next I called my colleagues at the Natural History Museum. I was welcome to bring in the boxes and they could freeze them for some days to some unimaginably low temperature, which was their way of dealing with such issues. In fact, all new material donated gets frozen down this way. But, yes there seemed to be some papers indicating that the microwave approach should work. Since I was leaving for home in Manila in a few days’ time, I decided on the microwave. Another test was done with infected and non-infected butterflies from the same box for eight minutes. They were left in the microwave overnight. No traces of pest activity were visible next day. I then zapped the box itself for eight minutes; all still seemed well. I opened the next box, put the box and its contents in the microwave, turned it on for eight minutes and went to the neighbourhood shop for a few essentials. When I entered the driveway to our building I was mildly surprised to see what looked like a slight haze through the windows of our large studio-flat. There was a smell of naphthalene when I opened the joint front door and when I opened the door to our flat a white cloud of evil-smelling smoke billowed out, forcing me back out in the open. There had evidently been plenty of naphthalene in the box and the microwaves had turned it to gas. I took a deep breath, rushed in, opened the back windows, and returned outside. After five minutes I took another deep breath to open the front windows, barely managing to get out in time. Then another dive into the flat to get something to read on the front stairs. Half an hour later seemed safe to enter the flat. The smell was still terrible, but it was possible to read near the open window. Whether it would be possible to sleep in my own bed that night was far from clear. The box of papered butterflies was a sorry mess. The volatile substances had obviously turned to gas. The remainder had absorbed lots of moisture, now NOTES 43 congealed with the paper triangles to a solid lump - enclosing one of the candidates for species novo. To add insult to injury, the remaining six boxes of papered material were all well stocked with camphor and free of pests: much ado about nothing ... as someone once put it. But it is a reminder that chemicals and medicines do have to be handled with care and that some of the rules and regulations pertaining to this may well have merit. My first killing medium for butterflies was potassium cyanide, a substance as toxic as they come. There was a procedure on how to get it in Denmark. You obtained a letter from your local entomological or natural history society testifying that you were an upstanding member with a genuine interest in insect collecting. You went to your police station and filled in a simple form, requesting a killing bottle. A few days later you received a slightly bureaucratese letter stating: “The police in Kastrup have no reason not to approve that 25gr of the requested chemicals are issued to the requiree provided that they are embedded in plaster of paris by an approved chemist [see list below].” One of the two chemists on the list below would duly make up an appropriate killing bottle, with adequate safeguards for the entomologist and the general public. When my Danish killing bottles weakened after several years’ of intensive collecting in Lebanon during the early 1970s, Henri Stempffer (“Master of the African Blues”, Ent. Rec. J. Var, 104:171-172 (1992)) came to my rescue, giving me enough industrial cyanide to last my time in Lebanon (industrial cyanide is not as pure as that from chemists and is actually better because its toxic gas develops faster). In 1975 I moved to London. We bought a large flat in Jackson’s Lane, Highgate (I hate to think what it would be worth today). When well installed, I went down to the local police station: “I need a certificate to buy cyanide”, I said to the station officer. “Cyanide, Sir!?!?” I explained the Danish procedures. It was a lazy afternoon - we were not good at crime in Highgate - so other officers joined in, but the conclusion was clear: “Sorry, Sir . . . we don’t do that kind of thing”. I called a colleague at the then British Museum (Natural History). Given all the material I had donated, he thought they could do me some killing jars. I was afraid I might need much more help than that in my future butterfly research, so I demurred: I was put through to their laboratory. They got their cyanide from a company in Enfield. I called Enfield: “Do you stock cyanide?” They did. “I’d like 250gr”. “Sorry, we only sell by the kilo”, said the bright young lady at the other end of the line. A kilo was something like £2.68 + VAT. “So what are the conditions of sale?” I asked. The answer was as precise as it was instantaneous: “You have to pay in advance” (a very British response indeed). I gave my office address and sent off a cheque. Two days later our receptionist phoned me: “Your cyanide has just arrived”. I went down and picked up a package with one kilo of cyanide. I suspect that the bright young lady at the other end of the telephone transgressed some company and/or government guideline on the sale of cyanide. But then again . . . who would order a kilo of cyanide if they did not need it? But that kilo of cyanide lasted me for the next fifteen years till I gave up using it. — Torben B. Larsen, UNDP Vietnam, c/o Palais des Nations, 1211 Geneva 10, Switzerland. 44 ENTOMOLOGIST'S RECORD, VOL. 119 25.i.2007 Acleris logiana (CL) (Lep.: Tortriddae) on Guernsey Late in the evening of 12 November 2005 I found a pale tortricid moth resting on the wall of my house under an outside light. At first glance I took it to be Acleris boscana (Fabr.) but elm, once the dominant tree on the island, has now mostly disappeared and I do not see the moth as often as I once did. In any case, its appearance did not seem quite right for boscana and, besides, I did not recall ever seeing it at such a late date. I dissected the genitalia, unfortunately making rather a poor job of it, and was no further on with identifying the moth until I showed the set specimen to Dr Phil Sterling on one of his visits to Guernsey. He immediately recognised it as Acleris logiana, a species new to the Channel Islands. Acleris logiana, which was previously thought to be a resident only of Scotland in the British Isles, was found in South Hampshire (VC 11) as larvae in spun birch leaves by John Langmaid in late 1991 (1993. Ent. Gaz. 44:154) and the annual reviews of microlepidoptera published in this journal since then note that it has been recorded subsequently from North Hampshire (VC 12) and a further six vice- counties in southern England, namely the Isle of Wight (VCIO) in 1997, East Suffolk (VC25) in 2000, Berkshire (VC22) in 2004 East Norfolk (VC 27) in 2004, North Essex (VC 19) in 2005 and West Suffolk (VC 26) in 2005. Its appearance on Guernsey (VC 11 3) suggests a further spread, although it is unlikely to survive here for long, if at all, as there is only a small amount of planted birch on the island. It has not been recorded from Normandy since the 1930s and never from La Manche, that part nearest the Channel Islands (Quinette, pers. comm.). — P. D. M. Costen, La Broderie, La Claire Mare, St. Peter’s, Guernsey GY7 9QA (E-mail: pcosten@guemsey.net). Caterpillars drinking ‘sugar’ At dusk on 28 September 2006, at my home address in Banffshire, two caterpillars joined the array of autumn moths on my line of sugared fence posts. One was a final instar Ruby Tiger Phragmatobia fuliginosa, the other a Scalloped Hazel Odontopera bidentata of the striking Tichened’ form. Ironically, I have never recorded the adults of either species at my sugar patch. Ruby Tiger, of course, does not feed as an imago. Scalloped Hazel certainly has a functioning proboscis, but I have rarely seen it feeding, and then only at the honeydew produced by aphids on sycamore leaves. — Roy Leverton, Whitewells, Ordiquhill, Comhill, Banffshire AB45 2HS. Third British record of Uloma culinaris (L.) (Col.: Tenebrionidae) from southern Hertfordshire On 2 September 2006, while collecting insects along the canal towpath near Casiobury Park in Watford, Hertfordshire (VC 20), my son Conall handed me a female Uloma culinaris. The beetle had been active on the surface of a fallen Fagus, the bark of which was mostly missing and the wood wet and hosting several different bracket fungi. Parts of the trunk were infested with Sinodendron cylindricum (L.) and NOTES 45 the lycid Platycis minutus (Fab.) was in abundance both on the wood and the surrounding nettles. Searching for another hour or so while the bright sunshine continued failed to reveal other specimens, as did subsequent visits during September. This is the third British record of Uloma culinaris. The first, from ‘Bushey Hall’ in 1950, is thought to relate to the Hertfordshire Bushey Hall, only a few miles from the present site (see Barclay, Ent. Rec. 115: 181 - 186). The only other record is of specimens collected from the Forest of Dean in 1973 by Wormesley and donated to the BM(NH). I thank Mr Trevor James for confirming the identity of my U. culinaris and both Mr James and Mr M. V. L. Barclay for encouraging me to report this find. — D. Murray, Flat 2, 52 Marlborough Road, Watford, Hertfordshire WD18 OQB. Acleris Upsiana (D.& S.) (Tortriddae) and Eudonia lineola (Curtis) (Pyralidae) new to the Shetland Isles Amongst a number of micro moths sent to me for genitalia examination from the Shetland Isles this year was a male Acleris Upsiana caught by Terry Rogers at Lea Gardens, Tresta, West Mainland on 22 September 2006. The larva of Acleris Upsiana is associated with Myrica gale, Vaccinium myrtillus and V vitis-idaea and the species is apparently restricted to upland areas northwards from the north of England and across the Scottish mainland. However, it is not yet recorded from Orkney (John Langmaid, pers. comm.) and the present records appear to be the first for the Shetland Islands (VC 112). The trap site is one of few well-stocked, mature gardens, situated on the side of expansive moorland with Vaccinium myrtillus away from Lerwick and regularly hosts ‘new’ species to this northern islands fauna. Perhaps less surprising, though nevertheless apparently also new to Shetland, were two examples, one male and one female, of Eudonia lineola both caught at Virkie at the southern tip of Mainland by Paul Harvey on 26 July 2006. This moth, whose larvae feed on lichens growing on trees and rocks, is widely distributed, albeit rather locally, across Scotland as far north as West Sutherland (VC 108), with an unconfirmed record from the Orkney Islands (VC 111). My thanks go to Matthias Nuss (Museum fiir Tierkunde, Dresden), for confirming my identification of Eudonia lineola, to John Langmaid (Southsea) for confirming the status of these moths in Shetland and to the Shetland team, mainly Paul Harvey, Mike Pennington and Terry Rogers, for continuing to send material to me. — Jon Clifton, Kestrel Cottage, Station Road, Hindolveston, Norfolk NR20 5DE (E-mail: jon.clifton@btintemet.com). Stauropoctonus bombycivorus (Gravenhorst) (Hym.: Ichneumonidae) new to the Isle of Wight On 5 August 2006, Tim Norris, James Halsey, Peter Cramp myself set up lights in Parkhurst Forest. One of our captures was a large ichneumon fly which was identified from a photograph as Stauropoctonus bombcivorus, a rare species which 46 ENTOMOLOGIST'S RECORD, VOL. 119 25.i.2007 has only previously been recorded from Windsor Forest and the New Forest. It is said to parasitise the Lobster moth Stauropus fagi (L.). This appears to be the first record for this species for the Isle of Wight. — Sam Knill-Jones, 1 Moorside, Moons Hill, Totland, Isle of Wight P039 OHU. Perils of the vernacular The name “Scarlet Malachite Beetle” for Malachius aeneus L. (Melyridae) {Ent. Rec. 118: 179) gives a somewhat confused idea of its colouring to anyone not acquainted with the species. It is, indeed, rather extensively scarlet, or at any rate red; however, malachite is not a red but a green mineral (hydrated copper carbonate). The choice of name for the beetle was probably influenced by the generic name Malachius, unconnected with the above, but apparently suggested by the Greek malakos, meaning “soft”, as in Malocodermata - the soft-skinned beetles. — A. A. Allen, 49 Montcalm Road, Charlton, London SE7 8QG. Avian predation of Sand Dart Agrotis ripae Hb. (Lep.: Noctuidae) Tutt’s (1901) Practical Hints for the Field Lepidopterist describes how imagines of Sand Dart Agrotis ripae may be found abundantly under pieces of driftwood lying on the shore above the high tide mark. I decided to put this to the test when visiting St. Cyrus (the village, not the holy man) in Kincardineshire with Mark Young on 28 June 2005. The dunes there are a good site for this species. Most of the driftwood present consisted of old bleached boughs of pine and other trees. Their irregular shapes left gaps and hollows beneath them, suitable places for a moth to hide. Very quickly I found the first Sand Dart - or rather, part of one. Only its disembodied wings remained. At least this seemed a promising start, but my confidence was misplaced. Further searching produced just more sets of wings. Then I noticed that every piece of driftwood was circled by the delicate tracks of Meadow Pipit Anthus pratensis, the imprint of its long hind claw clearly visible in the fine sand. The whole beach had been systematically worked already! I failed to find a single live moth by this method, though did see one later, nectaring on a hogweed head after dark. We were also pleased to find two freshly emerged examples of Shore Wainscot Mythimna Uttoralis, again at hogweed. St. Cyrus is its northernmost site in Britain and these were the first records there for over a decade. — Roy Leverton, Whitewells, Ordiquhill, Comhill, Banffshire AB45 2HS. BOOK REVIEWS 47 SUBSCRIBER NOTICE We are undertaking a molecular study on the phylogeny of the snakeflies (Raphidioptera) and we urgently need one or two specimens of Atlantoraphidia maculicolUs (one of the four British species in this group) preserved in alcohol of high concentration (if possible 96% or so). If the specimens are not older than five to ten years, then alcohol of a lower concentration may be suitable. Dried specimens are not required. Preserved larvae would also be useful. — Prof. Dr Horst Aspock, Department of Medical Parasitology, Clinical Institute of Hygiene and Medical Microbiology, Medical University of Vienna, Kinderspitalgasse 15, 1095 Wien, Austria (E-mail: horst.aspoeck@meduniwien.ac.at). BOOK REVIEW Moths of Europe, Volume 1: Saturnids, Lasiocampids, Hawkmoths and Tiger Moths by Patrice Leraut. 395pp.; 77 colour plates. 200 x 130 mm., hardbound. ISBN 2 913688 07 1 (English language version) and 2 913688 06 3 (French version). NAP Editions, 2006. €59 plus €7 postage and packing. Available from the publisher at 3 chemin des hauts graviers, 91370 Verrieres le Buisson, France, or via www.napeditions.com NAP Editions is a relatively new name to the world of natural science publishing, the book under review is their fourth production. The previous three excellent books concentrate on the various families of Coleoptera (Coleopteres de V Europe, available in French only), all written and illustrated by Gaetan de Chatenet, who is also responsible for the Preface in this present volume. Patrice Leraut is an authority on the Lepidoptera of France and Europe and has a great many publications to his name, but this work must surely be the culmination of his researches into the fauna of Europe. Published in French and English simultaneously, Moths of Europe covers the families Arctiidae, Sphingidae, Lasiocampidae, Saturniidae, Endromidae, Lemoniidae, Bombycidae, Drepanidae, Axiidae, Limacodidae, Notodontidae, Lymantriidae, Brahmaeidae, Castniidae, Heterogynidae, Somabrachyidae, Cossidae, Hepialidae, and Thyrididae, with 445 species described. Three new species {Cilix algirica Leraut, Heterogynis valdeblorensis Leraut and Heterogynis pravieli Leraut) are described as well as five new subspecies and five new forms. The male genitalia are drawn for the first two but, oddly, not for H. pravieli. One is inevitably led to wonder why new species are described in a book that is clearly intended for the popular market and which contains such basic material as “what is a moth”; it would surely be usual, and perhaps more acceptable to fellow researchers, for new species to be described in one of the many peer-reviewed journals? 48 ENTOMOLOGIST'S RECORD, VOL. 119 25.1.2007 The format follows the well tried and excellent system of their other publications; there is an introduction dealing with anatomical details, habitats (with examples of species to be found in each), collecting, identification, conservation etc. The text for each species is extremely informative including scientific, French and English names, description, variation, similar species, flight time, biology, status and distribution with maps. The colour plates are grouped together and are of excellent clear and well detailed quality. To include the large number of species, the moths depicted are not necessarily life size, although of the same scale on each plate. Actual size is mentioned on the opposite page also containing the identification and number of the text page. However, the caption pages facing plates 47, 48, 49 were evidently overlooked; they remain in French. Although the colours are natural, there is a certain overall greyness to the plates due to the reverse impression showing through. This may be due to the use of paper of a lighter weight than that used in their Coleoptera books, where this phenomenon does not occur. As stated the text is extremely informative, but some confusion could be caused by the distribution maps. For example, the map for Daphnis nerii (L) (Sphingidae), shows “black” throughout Europe, except north of Finland. The text explains that this shows the maximum migration zone, and then mentions it is exceptional outside its natural habitat. It would have been better if the “natural habitat” had been marked in black and the limits of migration indicated by something like hatching. There are other anomalies within this family and doubtless elsewhere. Comparative line-drawings of genitalia, wing venation and wing patterning are generously provided where species are difficult to separate, an extremely useful tool when this book deals with so many forms and subspecies. There is one contentious detail in this book, however, and that is the choice of vernacular names. A paragraph at the beginning of the book perfunctorily deals with this. There has already appeared in the pages of Entomologist’s Record a considerable discussion on this subject, to which I now add. Normally each country has its own name for a species, (e.g. Red Admiral becomes Vulcan in France) so that the British List will have Latin and vernacular names. It becomes ridiculous for a species endemic to, for example, a mountain or narrow habitat in the Urals to be given an English name. In this book EVERY species has been given an English name. Those on the British List are naturally given their habitual vernacular names, the remaining are given either a literal translation of the French or else a meaningless and/or confusing English appellation. For example, members of the genus Dyspessa (Cossidae) are given the common name of Mottled. Dyspessa emilia is highly local and endemic to Sicily; the French name is “marbrure du Peloponnese” and for the English version we have the Pelops Marbled! There are other examples. For example, a book quoted in the bibliography, and regarded as a reference for this present work, gives one English name for a satumid whilst in the present work there appears a different one I Discounting the vernacular names, which have been supplied by Robin Howard, the translation by Nicholas Flay is superb. This new book from Dr. Patrice Leraut, showing new species and illustrating many new forms gives that impetus to look again at one’s collection to find those subspecies which may have been overlooked. A great book necessary for all those interested in European Lepidoptera Further volumes are eagerly awaited. Michael Marney A BOOK FROM Experience the lighter side of field entomology with Torben Larsen as he describes his experiences from around the world. There must be a Hazard for every occasion? £11.99 (inc. UKp&p) *£13.99 (overseas) ORDER YOUR COPY NOW FROM Cravitz Printing Company Limited 1 Tower Hill, Brentwood, Essex CM14 4TA. Tel: (01277) 224610 • Fax:(01277) 262815 • E-mail: CravitzPrinting@btconnect.com THE ENTOMOLOGIST’S RECORD AND JOURNAL OF VARIATION http://www.entrecord.com Papers The immigration of Lepidoptera to the British Isles in 2003. Sean Clancy and Bernard Skinner 1-41 Notes Hazards of butterfly collecting. It seemed a good idea at the time: London 2001. Torhen B. Larsen 42-43 Acleris logiana (Cl.) (Lep.: Tortricidae) on Guernsey. P. D. M. Costen 44 Caterpillars drinking ‘sugar’. Roy Leverton 44 Third British record of Uloma culinaris (L.) (Col.: Tenebrionidae) from southern Hertfordshire. D. Murray 44-45 Acleris lipsiana (D.&S.) (Tortricidae) and Eudonia lineola (Curtis) (Pyralidae) new to the Shetland Isles. Jon Clifton 45 Stauropoctomis bombycivorus (Gravenhorst) (Hym.: Ichneumonidae) new to the Isle of Wight. Sam Knill-Jones 45-46 Perils of veracular. A. A. Allen 46 Avian predation of Sand Dart agrotis ripae Hb. (Lep.: Noctuidae). Roy Leverton 46 Subscriber Notice Atlantoraphidia maculicollis required. Prof. Dr Horst Aspbck 47 Book Review Moths of Europe, Volume 1: Saturnids, Lasiocampids, Hawkmoths and Tiger Moths by Patrice Leraut 47-48 SMITHSONIAN INSTITUTION LIBRARIES 3 9088 013271655 Printed in England by Cravitz Printing Company Limited, 1 Tower Hill, Brentwood, Essex CM14 4TA. Tel: 01277 224610 PUBLISHED BI-MONTHLY Edited by C.W. PLANT, Mc§ch/April ISSN 0013-8916 THE ENTOMOLOGIST’S RECORD AND JOURNAL OF VARIATION World List abbreviation: Entomologist's Rec. J. Van http ://www.entrecord.coin Editor C.W. PLANT, B.Sc., F.R.E.S. 14 West Road, Bishops Stortford, Hertfordshire CM23 3QP. Telephone/Facsimile: 01279 507697 E-mail: cpaukl @ntlworld.com Registrar Treasurer R.F. McCormick, f.r.e.s. C.C. Penney, fr.e.s. 36 Paradise Road, 109 Waveney Drive, Springfield, Teignmouth, Devon TQM SNR Chelmsford, Essex CM I 7QA WHERE TO WRITE EDITOR: All material for publication, including books for review and advertisements REGISTRAR: Changes of address TREASURER: Subscriptions and non-arrival of the Journal Readers are respectfully advised that the publication of material in this journal does not imply that the views and opinions expressed therein are shared by the Editor, the Entomologist’s Record Committee or any party other than the named author or authors. Entomologist’s Record and Journal of Variation is a non profit-making journal, funded by subscription, containing peer-reviewed papers and shorter communications. It is published by the Entomologist’s Record Committee, comprising the Editor, the Registrar and the Treasurer, from the Editorial address. An Editorial Advisory Panel exists to assist the Editor in his work. The annual subscription for year 2007 is £28 for individual subscribers or £50 for institutions. INSTRUCTIONS TO CONTRIBUTORS • This journal publishes peer-reviewed papers and shorter Notes that are reviewed by the Editor. Contributions are accepted on merit, with no regard whatsoever to the occupation or standing of the author. All contributions should bear the name and postal address of the author(s), but titles or honours are not permitted and will be removed. One e-mail address may also accompany the contribution. First time authors and non-subscribers are welcome to send material for publication. We are able to include colour photographs from time to time at no cost to the author(s). Good quality monochrome photographs are always welcomed. • The journal is concerned with British Lepidoptera (moths and butterflies). We also accept contributions on British Coleoptera (beetles), British Diptera (flies) and other groups at the Editor’s discretion. We also print Subscriber Notices at no cost on behalf of current subscribers; non-subscribers pay a fee for this service. We also publish Reviews of entomological books and other publications relating to all aspects of world entomology if these are sent to the Editor at no cost to him. It is our policy not to accept unsolicited book reviews from third parties. • We may also accept contributions on European insects if these are likely to be of interest to British readers, such as species likely to colonise Britain (especially where these contributions include identification keys or photographs), or accounts of entomological trips to places that may be of interest to other readers. • Papers should be at least 2000 words in length. Acceptance is not automatic. They will be peer-reviewed by two referees. Authors must be prepared to make modifications suggested by the referees. Papers must cover their subject matter to a far greater depth than Notes and should present original material or a broad-based review of existing knowledge. Descriptions of new species may be submitted. Authors of papers are expected to follow the house style and conventions as closely as possible. The Editor reserves the right to convert papers into Notes. • Notes are the meat of the journal! Most contributions will fall into this category. They will normally be less than 1500 words in length and can be very short indeed as long as the information they impart is interesting. We welcome Notes. There is no limit to how many you can contribute. Authors of Notes should try as far as possible to follow the house style and conventions, but the Editor will attend to these if errors are made. • We accept all formats from hand-written notes upwards. However, we prefer submissions via e-mail, or on CD. Files must be in a PC -compatible format that is readable by Microsoft Word. Originals are required for all photographs, drawings, diagrams, graphs, histograms and similar, though Tables may be incorporated into word processor files. For details, visit the web site or contact the Editor direct. BUTTERFLIES ON FARMLAND 49 BUTTERFLIES ON FARMLAND: THE FIRST 10 YEARS OF RECORDING AT WRITTLE COLLEGE ' R. G Field and ^T. Gardiner ' Butterfly Conservation, Cambridgeshire & Essex Branch, 166 Sherwood Avenue, Northampton, NN2 8TE, rfield8633 @aol. com ^ Writtie College, Lordship Road, Writtle, Chelmsford, Essex, CMl 3RR Abstract Butterflies were monitored over a 10 year period on two transects at Writtle College, Essex, UK. The transects were established in 1996 using the criteria established for the National Butterfly Monitoring Scheme (BMS). Numbers of butterflies observed have varied from a high of 2875 in 1997 to a low of 1215 in 2002. Overall 10 species (42%) are in decline, three (12.5%) are increasing, eight (33%) are stable while three species (12.5%) have been lost. Reasons suggested for these changes are varied and complex. An overall downward trend in abundance has occurred even though the College estate joined the Countryside Stewardship Scheme in October 1996, had a Woodland Grant Scheme agreement on certain sections and several areas of wildflower meadow had also been created. Introduction The agricultural landscape has changed dramatically since the 1940s mainly due to the intensification of arable systems (Dover, 1997). Much has been lost including 97% of lowland flower-rich grassland, 40% of lowland heath and 80% of chalk and limestone grassland (Asher et aL, 2001). Up to the introduction of the Countryside Stewardship Scheme (CSS) in the 1990s, hedgerows had also suffered with an estimated 67% loss in England (Asher et aL, 2001) and many more managed in a non wildlife friendly manner by regular trimming. These losses plus the use of pesticides and fertiliser during farming operations (Boatman, 1992), the change from haymaking to silage and the intensification of forestry operations has meant further fragmentation of semi-natural habitats (English Nature, 1995). This has had a negative effect on the native flora and fauna which inhabits farmed areas. Thomas et al. (2004) identified that 7 1 % of British butterfly species have declined over the last 20 years compared to reductions in species richness of 54% in native birds and 20% in plants. It is therefore suggested that butterflies are more sensitive to habitat change and destruction and could be used as early warning indicators of biodiversity loss. A method for surveying butterflies was established in 1976 with the creation of the Butterfl.y Monitoring Scheme (BMS) (Pollard & Yates, 1993). This scheme was used by the Centre of Ecology and Hydrology (CEH) to monitor butterflies at over 100 sites across the UK (Sparks et al, 2000). These, along with at least 500 additional transects undertaken for Butterfly Conservation (Asher et aL, 2001) are the best indicators of butterfly change. However, most of the sites involved in the scheme are nature reserves or other protected areas. Very few sites are on farmland and knowledge of butterfly population in these areas is limited (Sparks et al, 2000). 50 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 As farmland constitutes 65% of the land area in Essex and is potentially a very valuable habitat, this information forms an important indication of the health of wildlife in the county. The aim of this paper is to ascertain the main changes in butterfly abundance over 10 years on the predominantly agricultural Writtle College estate in Essex, UK. Methods Writtle College is located in the south-east of England, two kilometres west of Chelmsford in Essex (TL 670070). The College estate extends over 210 hectares and consists of agricultural, horticultural and conservation areas with landscaped amenity sites in the College grounds. From the mid 1970s, many conservation areas have been established and these include mixed broadleaf plantations, wildflower meadows in field corners and re-instatement of hedgerows along old field boundaries (Field & Gardiner, 2001). The method used for surveying butterflies was adapted from that used in the Institute of Terrestrial Ecology’s (now CEH) BMS (Pollard & Yates, 1993). This involves recording all butterflies seen within five metres of an observer whilst walking a set transect route, when the weather conditions are suitable. In 1996 two transects were created on the estate, the College Transect and the Lordships Transect (Table 1). These two routes, 5993 m in length, covered a large proportion of the farmed estate and the conservation areas, following the field boundaries where butterflies would be concentrated. The College Transect was divided into nine sections comprising different habitat types whilst the Lordships Transect had eight sections. These two transects were taken into the BMS scheme from 2001 and formed some of the few transects set up on intensively managed farmland. The surveys were conducted using the criteria outlined in Pollard & Yates (1993) once a week from April through to September for ten years beginning in 1996. A total of 26 weeks were to be surveyed each year although in most years unfavourable weather meant some surveys had to be abandoned. In the BMS because of the difficulty of distinguishing Thymelicus lineola and Thymelicus sylvestris in flight, both species were recorded combined as Thymelicus species. Data for both species are also combined in the results. The scientific names follow those in Asher et al. (2001). Each monitoring year on the Writtle transects (data for both combined) and the BMS (data for all BMS sites n UK combined) was given a rank according to the total butterfly abundance. The year with the highest number of butterflies recorded was given a rank of 1, and year with the lowest abundance a rank of 10. Spearman’s rank correlation (r^) was used to compare the ranks for both the Writtle data and the BMS data to ascertain whether the trends observed were comparable. Spearman’s rank correlation was also used to compare the total number of butterflies each year with the total rainfall in the preceding summer (ApriLSeptember) to determine if abundance is affected by rainfall as in the studies of Pollard (1988). To ascertain if butterfly species were substantially declining or increasing the total number of butterflies per year for each species were either compared for the periods BUTTERFLIES ON FARMLAND 51 1996-2000 and 2001-2005 or 1996-1999 and 2000-2005 using Mann Whitney U test. The periods compared differed because species have declined substantially since either 1999 or 2000 and the statistics needed to reflect this. To examine fluctuations in abundance for selected species, Chi-square (x^) analysis was used. Observed and expected butterfly numbers for each year were compared. Results The total number of butterflies observed on the transects has varied from a high of 2875 in 1997 to a low of 1215 in 2002. There is a strong relationship (P<0.01, r^ = 0.88, n = 9) between the number seen per year on the Writtle transects and the number seen per year on the BMS transects. The species richness has fluctuated between 24 in 1996 and 18 in 2005 (Table 2). Seventeen species have been recorded every year but three species have disappeared in the last few years. Lasiommata megera and Aphantopus hyperantus have not been observed since 1997 while Aricia agestis has not been seen since 2000. Two species, Cynthia cardui and Colias croceus, were occasionally recorded in years when high numbers of migrants reached UK shores and Lycaena phlaeas was not recorded on the transects every year but is known to be in low numbers in certain areas across the estate. Several species have sustained reductions in abundance over the 10 year period (Table 3). Ochlodes venata has significantly reduced since 1999 (P<0.05, U = 1, n = 4, 6) while Anthocharis cardamines has significantly reduced (P<0.05, (7 = 3, n = 5, 5) since 2000. Inachis io abundance has also significantly reduced (P<0.01, [/ = 0, n = 5, 5) since 2000. There have been several species where the abundance has increased over the 10 years. Pararge aegeria abundance has increased significantly (P<0.01, U = 0, n = 4, 6) since 1999 as has abundance in both Polygonia c-album (P<0.05, U = 2, n = 5, 5) and Maniola jurtina (P<0.01, U = 0, n = 5, 5) since 2000. Two species have seen large fluctuations in abundance over the period. Aglais urticae abundance has varied significantly (P<0.01, x^ = 31, n = 10) from 438 in 1997 to 1 in 2001 before rising again to 284 in 2004. Coenonympha pamphilus abundance has varied from 69 in 1996, 1 in 1999/2000/2002, 0 in 2001 and then back to 25 in 2005 (Table 3). There was a significant relationship (P<0.01, rg = 0.85, n = 9) between butterfly abundance and low rainfall during the months April to September of the previous year (Table 2). Out of the 24 species observed over the ten years 10 were in decline, three were increasing, eight remained stable and three were lost. Discussion The relationship shown between the Writtle transect data and the BMS data suggests that fluctuations identified at Writtle are generally reflect the changes happening throughout the UK. The species richness has reduced by three species when account has been taken of the migrant species. The first species lost was L. megera, and this follows a national decline in inland sites (Asher et al., 2001). The loss of 52 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 Table 1. Habitat type and management regimes for the two transects. College Transect Section Habitats Management Lordships Transect Section Habitats Management 1 WM Cut path (autumn) A WS A Cut grass margin 2 HM M cut for hay B HA Cut grass margin 3 HG Grazed C HA Cut grass margin 4 W A W non-intervention D HM M cut in Autumn 5 HMG Cut and grazed E H Hedge coppiced 6 WH A Arable F HA Cut grass margin 7 HA Arable G HO Cut track 8 M Cut for hay H H V Verge cut in Autumn 9 HS/S S/S cut in August Key: W = Woodland S/S = Set-aside S = Scrub H = Hedgerow A = arable field M = Grassy meadow G = Grazed pasture O = Orchards V = Roadside verge Table 2. Butterfly abundance and species richness. Year Number of Butterflies Species richness Rainfall Apr-Sept (mm) 1996 2664 24 161.3 1997 2875 22 226.7 1998 1846 20 352.9 1999 1793 19 285.5 2000 1648 21 346.5 2001 1409 18 384.3 2002 1215 19 272 2003 2349 20 181.3 2004 2729 20 339.1 2005 2168 18 427.2 BUTTERFLIES ON FARMLAND 53 Table 3. Individual species abundance 1996-2005. Species Total number Seen High Low Change Number of years seen Aglais urticae 2005 438 I sU 10 Cynthia cardui* 256 195 0 7 Inachis io 454 105 9 4. 10 Polygonia c-album 231 58 6 10 Vanessa atalanta 240 63 5 4^ 10 Aphantopus hyperantus 5 3 0 X 2 Coenonympha pamphilus 148 69 0 vb 9 Lasiommata megera 10 7 0 X 2 Maniola jurtina 4158 708 165 10 Pararge aegeria * 1352 248 25 10 Pyronia tithonus 3576 614 127 4. 10 Anthocharis cardamines 236 45 9 sb 10 Colias croceus* 13 9 0 3 Gonepteryx rhamni 41 12 2 10 Pieris brassicae 1204 219 41 10 Pieris napi 1677 466 21 sb 10 Pieris rapae 2394 493 111 "> 10 Aricia agestis* 63 56 5 X 3 Celastrina argiolus 135 58 4 sb 10 Lycaena phlaeas 25 8 0 sb 5 Ochlodes venata 406 199 1 sP 10 Polyommatus icarus 201 34 10 sb 10 Thymelicus spp. 2251 528 45 -> 10 * Not seen in 1976 survey (Neate, 1979) Increasing in numbers X Lost from the site between 1996-2005 ■=> Numbers stable Decreasing in numbers A. hyperantus was due to only a small area of suitable habitat being available. This was increased but the numbers were already too low to sustain the population. A. agestis has been increasing and decreasing its range in Essex over the last 15 years (Asher et al., 2001) and was seen for three years on the transects before disappearing again. 54 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 Three species have reduced in numbers, O. venata, having the largest fluctuations reducing from a high of 199 to a low of one. The reasons for these changes are not known as there was plenty of long grassy habitat which remained uncut and there were nectar sources nearby but it follows the national trend (Greatorex-Davis & Roy, 2005). A. cardamines has also reduced in numbers but this may be due to a run of poor spring weather over the last few years. The reason for the decline of /. io was unknown but reflects a national trend (Greatorex-Davis & Roy, 2005). Two species, A. urticae and C. pamphilus have had severe fluctuations during the last 10 year period. A. urticae had declined across the country but the decline was identified one year earlier in agricultural habitats (Field, 2002) than on the BMS transects. This species has since recovered to pre-decline numbers. C. pamphilus abundance was very low in the period 1999-2001 but since has made a slight recovery. The decline may have occurred because C. pamphilus favours short turf (Asher et aL, 2001) and those years had high summer rainfall which encouraged taller grass growth. Three species have significantly increased in numbers over the 10 years. The first species, P. aegeria, which was not present on the site in 1976 (Neate, 1979), has been increasing across the country (Asher et al., 2001) and from only small numbers at the start of the period was the third most numerous butterfly by 2005. The second species to increase in numbers was M. jurtina. This was not surprising as many wildflower meadows and pastures have been created on the College estate over the last 15 years (Field & Gardiner, 2001), thus extensive favourable habitat has become available. P. c-album, the third species to increase was following an increasing national trend which may be due to the more wildlife friendly management of hedgerows in agri-environmental schemes such as the CSS. Pollard (1988) suggested that there was a relationship between high butterfly abundance and low rainfall in the previous summer. The data collected from these transects and the Writtle College weather station also suggests such a relationship. Prime examples being 1997 with 2875 butterflies seen and a low rainfall of 161.3 mm in 1996 and 2004 with 2729 butterflies seen and a low rainfall of 181.3 mm in 2003. Thomas et al. (2004) identified that 7 1 % of all British butterflies were reducing in numbers but that included a wide range of our most threatened butterflies. This study at Writtle confined to only common butterflies suggests that 42% are declining, with 33% steady, 12.5% increasing and 12.5% lost from the College estate in the last 10 years. What must be remembered when looking at these figures is that everything possible has been done to manage the estate in a wildlife friendly manner for the last 15 years. The farm has been in CSS since 1996. During that time 2 and 6 m grass margins have been established, some hedges planted, others managed by coppicing and laying, and areas of woodland have been planted under the Woodland Grant Scheme. The field margins set up under the CSS were generally successful in increasing butterfly abundance but could have been far better habitats for butterflies had there been nectar sources available in the mixtures sown (Field et al., 2005a; 2005b; 2006; in press, Field & Mason, 2004a ; 2004b; 2005). BUTTERFLIES ON FARMLAND 55 Condesioes The analysis of long term data has shown worrying trends for common butterflies. Nearly 55% of species seen on the Writtle College transects are either in decline or have already been lost over the 10 years. This was all happening on a site managed positively for wildlife and especially butterflies. If such a large loss can occur on favourably managed farmland what can the effects be in the wider countryside? The grassland habitats established at Writtle were not on a small scale; they were field size and were interconnected by hedgerows, ditches, streams, permanent set- aside and wide grassy margins. One problem with some areas of the grass margins and pastures was that they were sown with commonly used cultivars of agricultural grasses and wildflowers. Recent research (Field, 2005) suggests that the use of native grasses and wildflowers, even though more expensive, can produce habitats which support four times the number of butterflies and significantly greater species richness. Most of the BMS sites are protected habitats, Sites of Special Scientific Interest or nature reserves, and as such hold strong butterfly populations. Using A. urticae as an example, declines were observed in the wider countryside first (Field, 2002) followed a year or so later by declines on the other BMS transects. That might suggest that for common butterflies the wider countryside is a better indicator of the health of a species than data from protected habitats. If the current rate of loss continues for the next 20 years another 4-6 species could be lost at Writtle and any of the 10 species in decline are at risk. This does not take into account any future effects global warming might have on habitat change and butterfly abundance and species richness. Acknowledgements The authors would like to thank other recorders such as Graham Watkins, Michelle Gardiner, Zoe Ringv/ood and Emma Sellers who have walked the transects on various occasions. References Asher, J., Warren, M., Fox, R., Harding, R, Jeffcoate, G. & Jeffcoate, S., 2001. The Millennium Atlas of Butterflies in Britain and Ireland. Oxford: Oxford University Press. Boatman, N.D., 1992. Herbicides and the management of field boundary vegetation, Pesticides Outlook, 3, 30-34. Dover, J.W., 1997. Conservation headlands: effects on butterfly distribution and behavior. Agriculture, Ecosystems and Environment 63, 31-49. English Nature, 1995. Rebuilding the English Countryside. Peterborough: English Nature. Field, R.G., 2005. Six metre grass margins and butterflies. Entomologist’s Record & Journal of Variation 117(6)i 271-273. Field, R.G., 2002, A study of butterflies on farmland. Unpublished PhD thesis. Colchester: University of Essex. Field, R.G. & Gardiner, T., 2001. Habitats and abundance of butterflies on agricultural land at Writtle College. Essex Naturalist 18: 129-138. 56 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 Field, R.G. & Mason, C.F., 2005. The utilisation of two metre Countryside Stewardship Scheme grass margins by the Gatekeeper Pyronia tithonus (L). Journal of Natural History 39 (18): 1533-1538. — , 2004a. The utilisation of two metre Countryside Stewardship Scheme grass margins by Meadow brown Maniola jurtina (L). Entomologist’s Record & Journal of Variation 116: 61-67. — , 2004b. The utilisation of six metre Countryside Stewardship Scheme grass margins by the Gatekeeper Pyronia tithonus (L). Entomologist’s Record. & Journal of Variation 116; 101-112. Field, R. G., Watkins, G. & Gardiner, T., 2005b. The use of Countryside Stewardship Scheme field margins by the Small skipper Thymelicus sylvestris (Poda), Essex skipper Thymelicus lineola (Ochs.) & Large skipper Ochlodes venata (Br. & Grey). Entomologist’s Record & Journal of Variation 117(5): 197-203. Field, R.G., Gardiner, T., Mason, C.F. & Hill, J., 2006. Countryside Stewardship Scheme and Butterflies: A study of plant and butterfly species richness. Biodiversity and Conservation 15(1)1 443-452. Field, R.G., Gardiner, T., Mason, C.F. & Hill, J., 2005a. Agri-environment schemes and butterflies: The utilisation of six metre arable field margins. Biodiversity and Conservation 14(8): 1969-1976. — , in press. Agri-environment schemes and butterflies: The utilisation of two metre arable field margins. Biodiversity and Consenmtion. Greatorex-Davis, J.N. & Roy, D.B., 2005. Butterfly Monitoring Scheme: Report to Recorders 2004. Monks Wood: CEH. Neate, D.J.M., 1979. Writtle Agricultural College Wildlife and Landscape Survey: Report and recommendations. Chelmsford: Writtle College. Pollard, E., 1988. Temperature, rainfall and butterfly numbers. Journal of Applied Ecology 25, 819-828. Pollard, E. & Yates, T., 1993. Monitoring Butterflies for Ecology and Conservation. London: Chapman and Hall. Sparks, T.H., Meek, W., Pywell, R.F. & Nowakowski, M., 2000. The influence of field margin management on the butterfly fauna of a Yorkshire arable fauna. In: Boatman, N.D., Clay, D.V., Goodman, A., Marrs, R.H., Marshall, E.J.P., Newman, J.R., Putwain, P.D. & Pywell, R.F. (Eds) Vegetation management in changing landscapes. Warwick: Association of Applied Biologists, pp 407-410. Thomas, J.A., Telfer, M.G., Roy, D.B., Preston, C.D., Greenwood, J.J.D., Asher, J., Fox, R., Clark, R.T. & Lawton, J.H., 2004. Comparative Losses of British Butterflies, Birds, and Plants and the Global Extinction Crisis. Science 303, 1879-1881. Cornifrons ulceratalis (Lederer^ 1858) (Lep.: Crambidae) new to France and Syncopacma albifrontella (Heinemann, 1870) (Lep.: Gelechiidae): first published French record Perhaps being located at a geographical crossroads gives rise here to a climate different to that in other parts of south-west France? Squeezed between the Pyrenees and the Massif Centrale a corridor is formed, the Plaine Toulousaine, stretching as far north as Northern Tarn where we live. Winds from the south and south-east sweep up this gap, bringing with them warm air from the Mediterranean region. Thus we have both Mediterranean and mountainous species of Lepidoptera passing through. For this reason we keep a daily record of the temperature, wind force and NOTES 57 direction. When the wind is continuously from the east/south-east with fairly stable temperatures in the mid to high twenties, we keep a special look-out at our moth traps in the garden. In the past, this has rewarded us with surprise discoveries of Heliothis nubigera (Eastern Bordered Straw) and Lacanobia splendem (Splendid Brocade), but we surpassed this in the autumn of 2006 with two moths apparently entirely new to the French fauna. Cornifrom ulcerataUs: Prior to 27 October 2006, the wind had been blowing from the south-east and south for several days, with a temperature of 26°C max to 17°C min. Nothing ro.uch of interest was flying, that eight, but at LOO am, resting on the side of the trap was a small moth completely unknown to us. As we moved in for a closer look it flew off, and was put down as a question mark. When we came to close down the trap in the morning, there it was at the bottom of the trap. It was duly captured and set and digital images v/ere e-mailed to Colin Plant and Jon Clifton for an opinion; Jon also roped in Harry Beaumont; all three came back almost immediately with the same name - Cornifrons ulcerataUs, with Colin’s opinion based on first hand experience of the species and specimens in his collection. This moth is not included in the latest published list of French Lepidoptera (Leraut, 1997. Liste Systematique et synonomique des Lepidopteres de France, Belgique et Corse 2nd edition) and examination of the Fauna Europaea web site indicated that there were no more recent unpublished records. Syncopacma alMfmntella: Jon Clifton and his family made a visit to Gradde at the beginning of September, 2006, and on the night of 2 September the weather appeared favourable for mothing - at 30°C maximum and 18°C minimum, the wind from the south tending towards south-west. That night, we caught many examples of Syncopacma and a selection was taken for further study; Jon returned to UK and commenced the identification by means of genitalia dissection. Amongst the material collected was a male Syncopacma albifrontella which Colin Plant identified from the genitalia slide prepared by Jon. This species is not listed for France in Leraut’s first French checklist (1980), but does appear in thel997 second edition {op. cit.), though it is not immediately noticed since it is included (as species number 1758) in the genus Stomopteryx, for reasons which are not immediately apparent. The entry for this species on the Fauna Europaea web site was prepared by Dr Ole Karsholt and this also shows its presence in the country, but a search of the literature has failed to reveal any published reports. Dr Karsholt has, however, most kindly informed us that the basis for his inclusion of Syncopacma albifrontella as a French species is the presence of three males in the collections at the Zoological Museum of Copenhagen labelled "France, Dept. Hautes Alpes, Valle de la Romanche, les Freaux, 1400 m, 27. Hi. 2000, leg. P. Skou\ These do not appear to have been published in the literature and the opportunity is taken to correct that omission here. We are most grateful to Ole Karsholt, Zoologisk Museum, Copenhagen for clarifying the basis of his inclusion of Syncopacma albifrontella as a French species on the Fauna Europaea web site and for allowing us to include reference to the 58 ENTOMOLOGISTS RECORD, VOL. 119 25iii.2007 Copenhagen Museum specimens here. We would like to express appreciation to our friends Colin Plant and Jon Clifton for all their help and assistance and also to Mr Harry Beaumont for his consideration of the photographs via Jon. — - Michael & Brenda Marney, Gradde, 81140 Campagnac, France (E-mail: marney.michael @ wanadoo.fr). Nest building and prey stocking in Crossocerus megacephalm (Rossius) (Hym.; Sphecldae) Hatfield Forest in Essex is a large area of ancient woodland and wood pasture near Bishop’s Stortford. On several occasions during the summer months of 2006, Hymenoptera were seen around the upright remains of some of the dead birch, beech and oak trees. On 21 July 2006, a small hole, approximately 5mm in diameter, was spotted in dead stock arising from a hazel Corylus avellana coppice. A small pile of wood dust around the base of the stock indicated recent activity. The stock was investigated and it came away easily in its entirety. The dry, dead wood was split along its length and inside was a tunnel with three brood chambers, two of which were empty. The third chamber was tightly packed with what appeared to be small flies. The tunnels also contained two pale amber, hymenopteran cocoons. The spilt stock was taped back together and taken home. The next day, the extent of the nest within the stock was investigated under a dissecting microscope and the pupae were removed. Unfortunately, one of the pupae had been damaged when the stock was split open. The intact pupa was moved to a glass vial and left until the adult insect emerged. The three brood chambers were inspected; two contained nothing excect frass, whilst the third was stocked with flies and sealed with a plug of wood-dust. There were 15 flies in total and all appeared to be the same species, later confirmed by Jon Mellings who identified them as Chrysopilus asiliformis (Preyssler) (Rhagionidae). One week after the nest was closely examined, the pupa hatched and an adult sphecid emerged; this was identified by Jon Mellings as Crossocerus megacephalus. To the author’s knowledge, this is the first time a prey species has been identified for C. megacephalus. However, the observation does not provide any information on the prey preferences of this wasp. The fly could have occurred in profusion near the nest - alternatively the wasp may selectively hunt this small species. Regardless of the true nature of this relationship, the fact remains that a small wasp excavated an impressive nest in dead wood, and if the contents of the intact brood chamber are to go by, stocked it with at least 40 C. asiliformis. The possibility also exists that a mated pair of C. megacephalus work together to construct the nest and stock it with flies as two of these wasps were often seen around the same hole. If a pair of these wasps devoted their adult energies to a single nest then the reproductive strategy of this species could to be to produce a very small amount of well provisioned young.— Ross Piper, 17 Southmill Court, Southmill Road, Bishops Stortford, Hertfordshire CM23 3DA. (E-mail: ross_piper@yahoo.com). URESIPHITA REVERSALIS NEW TO BRITAIN 59 URESIPHITA REVERSALIS (GUENEE, 1854) (LER: PYRALIDAE) NEW TO BRITAIN AND EUROPE ’ Tony Davis and ^Doug Miller ' Timber Tops, Marley Common, Haslemere, Surrey GU27 3PT ^ Broad St one House, 1 Broadstone, Westonzoyland, Bridgwater, Somerset TA7 OEW Abstract Uresiphita reveralis Guenee (Lep.; Pyralidae) is added to the British fauna on the basis of a specimen taken in Somerset during September 2006; evidence suggests that this species has not previously been reported in Europe. The adult moth is illustrated in colour and details of its life history and distribution are given. The likely origin of the Somerset specimen is discussed. Introduction On the night of 23 September 2006, National Moth Night, DM ran a Robinson MV trap in his garden at Westonzoyland, Somerset (O.S. grid reference ST 3434). The trap was placed next to the cream-coloured garage wall as some of the more unusual moths do not enter the trap and are found resting on the wall. Westonzoyland is located on the edge of the Somerset Levels which has very few trees or shrubs and can be affected at times by strong winds. DM’s garden can best be described as untidy and is thus a haven for wildlife. The weather was warm with a little rain at times and a light wind from the south-east. Interesting moths recorded during the night included Four Spotted Footman Lithosia quadra (L.), Palpita vitrealis (Rossi), Silver Y Autographa gamma (L.), Vestal Rhodometra sacraria (L,), Udea ferrugalis (Hb.) and Nomophila noctuella (D.& S.) as well as the first Pinion Streaked Snout Schrankia costaestrigalis (Steph.) for the site. A single Uresiphita reversalis was immediately seen upon checking the trap. It looked familiar to DM, but checking through all the books available to him failed to produce a suitable match. The specimen was passed to David Evans who gave it to TD at the Annual Exhibition of the British Entomological and Natural History Society (BENHS). The unset specimen was shown to various lepidopterists at the BENHS exhibition, but an identity was not forthcoming. Upon relaxing, it was immediately apparent that it was related to Uresiphita gilvata Fabr. However it was significantly smaller than typical U. gilvata, had greatly reduced black on the hindwing and a relatively poorly marked forewing; a scan of internet images suggested that U. reversalis was a good match. After setting, the moth was photographed and the image sent to Martin Honey and Michael Schaffer at the Natural History Museum, London, who kindly confirmed the identification. Recognition The wingspan of the Somerset specimen was 26.5 mm, which is below the range of 29-37 mm given for U. gilvata by Goater (1986). Unfortunately, Munroe (1976) 60 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 does not give a size range for U. reversalis and it seems likely that there may be a small overlap in size between the two species. Both species have an orange-yellow hindwing with a blackish border but the border of U. reversalis is usually limited to the apex and rarely extends as far as half way along the border. In U, gilvata there is frequently a complete blackish border although it can occasionally be reduced, as in the illustration in Goater (1986). A couple of specimens in the Natural History Museum collections have the dark markings reduced to the hindwing apex (Martin Honey, pers. comm.). The forewing of U. reversalis is generally poorly marked and is often more orangey-brown than U. gilvata. The central part of the forewing is often the same colour as the rest of the forewing and if a dark bar is present, it is just a slightly darker shade of brown. Biology and distribution Munroe (1976) states that the larvae feed on the leaves and tender bark and shoots of broom. Genista sp., lupines, Lupinus sp.. Wild Indigo, Baptism tinctoria (L.) Necklace Pod, Sophora tomentosa (L.), honeysuckle Lonicera sp., and other plants and shrubs, especially legumes. Leen (1995) gives the distribution as being from Nova Scotia, Canada, down the eastern side of North America into parts of Mexico and extending west into Arizona and California. The current distribution in central and northern California is attributed to an expansion of range in the early 1980s. Munroe (1976) states that in the northern part of the range there are years of sporadic abundance, possibly sustained by migration from the south and that it is an occasional pest of nursery stock and ornamental plantings. There is no mention of this species in Karsholt & Razowski (1996) or on the Fauna Europaea website (http://www.faunaeur.org) so this appears to represent the first European record. It is suggested that it is allocated a logbook number of 1369a. Munroe (1976) gives the flight period as being from February to November in the southern part of its range. Origins Whilst it is always impossible to know for certain the origins of a particular specimen, and the fact that U. reversalis can occasionally be a pest of nursery stock points towards accidental importation, there are several factors which are indicative or natural arrival. The relatively rural location of the capture, on the western side of Britain during September is more indicative of natural arrival and fits with the predominant pattern of arrival of Nearctic birds and insects. Of particular interest was the discovery of two Buff-breasted Sandpipers Tryngites subruficollis and a Semipalmated Sandpiper Calidris pusilla at Slimbridge on 22 September. Slimbridge is approximately 80 kilometres north-east of Westonzoyland and the arrival of these birds indicates that the air currents in that part of the country were suitable for transatlantic vagrancy. URESIPHITAREVERSALIS NEW TO BRITAIN 61 Plate A. Uresiphita reversalis (Guen.), Westonzoyland, Somerset, 23.ix.2006, Leg. D. Miller. Photograph © Keith Tailby Acknowledgements We would like to thank Martin Honey and Michael Schaffer of the Natural History Museum, London for confirming the identity of the specimen. Barry Goater and Jim Porter kindly made relevant literature available to us. We are also grateful to Frantisek Slamka (Bratislava) for confirming that there do not appear to be any previous records of this species in Europe. We would also like to thank Simon Woolley for providing the information on Nearctic bird arrivals and Keith Tailby for photographing the specimen. References Goater, B., 1986. British Pyralid Moths. A guide to their identification. Harley Books. Karsholt, O. & Razowski, J. (Eds), 1996. The Lepidoptera of Europe. A distributional checklist. Apollo Books. Leen, R., 1995. Biology of Uresiphita reversalis (Guenee) and comparison with U. polygonalis maorialis (Felder) (Crambidae). Journal of the Lepidopterists’ Society 49(2): 163-170. Munroe, E., 1976. The Moths of America North of Mexico. Fascicle 13. 2 A Pyraloidea Pyralidae (Part). E.W. Classey Limited and The Wedge Entomological Research Foundation. 62 ENTOMOLOGISTS RECORD, VOL. 119 25iii.2007 The ad¥aiitages of ^Doing the Dirt”: New and interesting moth records for Hertfordshire & Middlesex When I look in the cabinets of ‘proper’ entomologists, I always feel slightly jealous of the rows of immaculate specimens - all pristine and shiny. Many of the specimens I have are retained in my collection are there merely in support of a genitalia slide that I have made from various specimens. Few are immaculate, some are passable and others look a lot like car crash victims! A great many of the specimens that I receive tend to arrive in various boxes marked ‘Micros 2006’ or the like (sound familiar?). You know most of them will be common, but there is always the prospect of finding something exciting in these ‘boxes of dirt’. Among the Hertfordshire (VC 20) and Middlesex (VC 21) specimens supplied to, or taken by, me this year the following were notable for the reasons stated: New to Hertfordshire (VC 20) Argyresthia cupressella Wals.: Bishops Stortford, 2.vi.2005 (J. Fish & J. Reeves); Acleris logiana (CL): Bishops Stortford, 29.1.2005, (J. Fish & J. Reeves). New to Middlesex (VC 21) Stigmella tiliae (Frey): Fir & Pond Wood Nature Reserve, mines, 19.x. 2006 (R. Terry); Niditinea piercella (Bent.): Fir & Pond Wood Nature Reserve, 16. vi. 2006, (R. Terry); Argyresthia cupressella Wals.: Wood Green, 9.vi.2006 (M. Ashby); Colephora vestianella (L.): Greenford, 06.vii.2006 (A. Culshaw); Cochylis molliculana Zell.: Horsenden Hill, Greenford,2Lvi.2003 (R. Terry). Predates the record on file from Kensington Gardens, 2.viii.2005 (T. Freed). Epinotia caprana (Fabr.): Fir & Pond Wood Nature Reserve, Lix.2006 (R. Terry); Strophedra niditana (Fabr.): Fir & Pond Wood Nature Reserve, 28.vi.2006 (R. Terry); Cydia conicolana (HeyL): Wood Green, June 2006 (M. Ashby); Hymenia recurvalis (Fabr.): Bamet, 28.x. 2006 (R. Terry). Significant updates to the Middlesex fauna 1 . Species for which the only known previous record was included in the distribution map in the relevant volume of Moths and butterflies of Great Britain and Ireland (Harley Books) but is unsupported by full data. Metzneria lappella (L.): Wood Green 10,vii.2006 (M. Ashby); Gelechia scotinella (H.- S.): Fir & Pond Wood Nature Reserve, 5.viii.2006 (R. Terry); Cnephasia longana (Haw.): Wood Green, 29. i. 2006 (M. Ashby). 2. Records that significantly update the lists presented by Colin Plant (2002. A provisional list of the microlepidoptera of Middlesex (VC 21). London Naturalist 81: 123 - 186 and 2004: Additions and corrections to the provisional list of the microlepidoptera of Middlesex (VC 21). London Naturalist 83: 107 - 109. Neofriseria singula (Stdgr.): Fir & Pond Wood Nature Reserve, 5.viii.2006 (R. Terry); NOTES 63 Lobesia botrana (D.& S.): Wood Green, 20.vii.2006. (M. Ashby); Last recorded at Hampstead, 1985; Ancylis mitterbacheriana (D.& S.): Fir & Pond Wood Nature Reserve, 3.V.2006 (R. Terry). Last recorded Ruislip, 1959; Ancylis laetana (Fabr.): Barnet, 9.viii.2006 (R. Terry). Last recorded Ruislip 1959; Paralipsa gularis (Zell.): Wood Green, 13.vi.2004 (M. Ashby). Last recorded at Finsbury Park, 1932 and Ruislip, 1957. I am grateful to Andy Culshaw, Marcel Ashby, James Fish and Julian Reeves for permission to include the records made from specimens collected by them in this summary. I also thank Colin Plant for double-checking some of the identifications made from my slides of genitalia and for confirming the status of the species listed. — Rachel Terry, 92 Woodville Road, Barnet, EN5 5NJ (E-mail: s wordgrass @ btintemet.com) . Editorial Comment: Rachel will probably hate me for saying it, but as a county recorder I would think the appellation 'proper entomologist’ would be far more appropriately applied to her good self and to anyone else who recognises the significance of the battered, scale-less ‘bits of dirt’ left over in the bottom of the moth trap after the mere collectors have had their turn! Late-flying Silver-ground Carpets Xanthorhoe montanata D. & S. (Lep.: Geometridae) in Banffshire Philip Gould’s note {Ent. Rec. 118: 227) reporting this species in a Rothamsted trap at Ben Eighe in West Ross on the late date of 2-5 September 2005 prompted me to check my own records for Banffshire. In nine of the 17 years from 1990-2006, I recorded this species in September at my home address. Most moths were in the first week, the latest date being 1 1 September 2002. Although the flight time given in the literature for this species is from mid-May to late July, in northern Scotland it emerges about a month later. My average date of first sighting during the years mentioned was 15 June (range 5-27 June), and the whole flight period is correspondingly delayed by about a month. Moths peak in July, but stragglers continue into early autumn in most years. It is very unlikely that such late individuals constitute a partial second generation. Those seen here are invariably female and often below normal size. Perhaps they are caused by some developmental abnormality, as they are much more frequent in cool summers than in warm ones. For instance, there were no September sightings here in 2003 or 2006, years when a wide range of other species produced unusual second broods. Indeed, the last sighting in 2003 was on 5 August, my earliest-ever final date. Also, I am currently rearing this species in captivity. From eggs laid in June 2006, the caterpillars developed very slowly and are still barely a centimetre long in early November. — Roy Leverton, Whitewells, Ordiquhill, Comhill, Banffshire AB45 2HS. 64 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 Notes on the early stages of Elachista regificella Sircom, 1849 and E. tengstromi Kaila et aL, 2001 On 26 April 2006, Norman Lowe and I visited Coed Fenni-fach, an area of woodland about 3km west of Brecon, by kind permission of the landowner, David Jones Powell. Here we found Luzula sylvatica and L. pilosa in plenty and in about equal quantity. In the previous year’s leaves of both plants were the typical inflated, puckered mines of Elachista spp. of the regificella Sircom group (Plates B & C). Plate C. Larval mine of Elachista regificella Sircom, on Luzula sylvatica. NOTES 65 The larvae were slow to mature, having formed new mines in the current year’s leaves, but eventually vacated their mines and pupated. Imagines of E. regificella emerged between 11 and 19 June from the L. sylvatica stock and E. tengstromi between 22 June and 2 July from that on L pilosa. The identity of the moths was confirmed by dissection of the genitalia. Although only a small number were reared, the dates of emergence may indicate that E. regificella is on the wing earlier than E. tengstromi. The larvae showed some differences in the final iestar and are described as follows: E. regificella. Head pale honey coloured, mouth-parts a little darker; prothoracic and anal plates and thoracic legs likewise; body greenish black. E. tengstromi. Head pale honey coloured, mouth-parts dark brown; prothoracic and anal plates and thoracic legs translucent yellowish green; body dull green, tinged yellowish ventraliy. Thanks are due to Ian Thiriwell for photographing the mines. — ■ John R. Langmaid, Wilverley, 1 Dorrita Close, Southsea, Hampshire P04 ONY. Hazards of butterfy collecting. Bumbuea Butterfly Survey - Sierra Leone, May 2006 We stood at the foot of the giant Bumbuna Dam in northern Sierra Leone, looking up-river. It promised to become a good day for butterflies. The morning mist was clearing and rain apparently did not threaten. As part of World Bank procedures an Environmental Impact Assessment had to be performed before the reservoir could be flooded. I was contracted to analyze the local butterfly fauna. The main threatened habitats were small patches of riverine forest fringing the Sell River, all of which would be flooded by the inundation of the reservoir, and was unlikely to regenerate. We were three people •- myself, my field assistant Nyakeh Mattia, and our driver Mohammed Deen. We were planning a walk that would take us further north than we had ever been in the narrow band of riverine forest, nearly all of it in poor condition. Various permutations of my team had been in the area several times before. Very little riverine forest still remained and most of that was inaccessible, so this area (“Rashida’s Forest” - as it was named after another team member) was subjected to in-depth study. We walked the first few kilometres as fast as we could in order to reach the parts of the forest that we knew less well and reached what seemed to be the highest quality bits. We gave these a thorough going-over and then decided to continue on into unknown territory. Our aerial photographs indicated that some forest patches would be found, but the photos were 15 years old, and they might have gone by now. Virtually all forest in the valley had been destroyed in favour of cultivation of mountain rice. Hundreds of square kilometres of steep hillsides were completely denuded and bits and pieces of forest remained only in inaccessible ravines and along the river. This destruction had little to do with the dam project. 66 ENTOMOLOGISTS RECORD, VOL. 119 25.iii.2007 Similar processes have reduced the forest cover in Sierra Leone to less than 5% of its original area - even worse than in most West African countries. Not wanting to put all our eggs in one basket, Mohammed was left in the good forest while Nyakeh and I would explore the unknown. Mohammed, being our driver, could have done as drivers do: stay behind and sleep in the car. But he had become keen on butterfly collecting and could now tell his Charaxes from his Euphaedra. A few days ago, when nothing new was being found, I decided to knock off early: we had not had a break for three weeks. “We can’t go now”, protested Mohammed, “we haven’t caught enough butterflies”. My chimpanzee-studying colleague, Chris Ransom, told me that each time he came to our office, Mohammed was engrossed in my book Hazards of Butterfly Collecting - a collation of the stories published in this journal. He had also become quite proficient at finding the relevant plates in Butterflies of West Africa during our butterfly identification sessions. In short, Mohammed was not your typical driver. Nyakeh and I pushed on along the narrow path. There was virtually no forest left, but in places there was quite tall bush-fallow (i.e. at least 15 years old), and we caught a few interesting species there. After that ecological conditions deteriorated. Was it worth continuing? The tendency is always to continue - there might just be a crock of gold around the next twist of the river. Eventually we were about an hour and half from Mohammed. Suddenly it clouded over, thunder boomed, lightning flashed, and the heavens opened up. We were wet through in minutes. At 3,700mm rainfall a year - five times more than in Denmark - the missing natural vegetation would have been rainforest [technically hyperwet evergreen forest], so you can’t really complain. But an hour on a slippery track, soaked, water squishing in your shoes, and with not a single butterfly in sight is still a somewhat unsatisfactory pastime. The rain stopped just as we reached Mohammed, who gave us a bemused look. Rain in the area can be amazingly local and he had not received a drop. He had also caught some useful butterflies. Cloud had obscured the sun so we decided to call it a day and make our way back to the dam. Then the heavens opened up again, just as Mohammed bracing himself for our next field trip shoes had stopped squishing. with Hazards of butterfly collecting. Mohammed was soon just as NOTES 67 drenched as we had been on arrival. A moment later, he turned towards me with a huge grin: “Hazards of butterfly collecting!” A more wonderful, quick-witted, and apposite comment could hardly be imagined - it collected a round of laughter and made the hour's wet walk back to the car more bearable, though the shoes still The car stood untouched by rain just 200m from where we were still being drenched. We had a drink and prepared to get back to base, when I remembered that I had pulled up a heliotrope plant to expose the roots. I had been showing my team the intricate androconial organs of the danainae and telling them of the need to tank up with pyrrolizidine alkaloids to secure sexual success. The first act of a male danaid is to fly off in search of plants containing pyrrolizidine compounds. Such plants can be scarce and localized and sometimes large numbers of males are found on a single plant - especially a damaged plant with dry bits. The heliotrope patch on the dirt road in front of the dam seemed to have the character of such a “pyrrolizi-diner”, so I had decided to give it a try: “Maybe they will attract the Amauris” We went to have a look. Sure enough ~ on the crumpled heliotrope, and especially on the roots, sat eleven males of three species of Amauris as well as a couple of Danaus chrysippus Linne, 1758. Such modest success does your role as team leader no harm! We took some fresh heliotrope back to the construction camp where we lodged and hung it on the boundary fence. Even after a week our bait was still attracting male danaids.— Torben B. Larsen, UNDP Vietnam, c/o Palais des Nations, 1211 Geneva 10, Switzerland. Amauris damocles on our dead bait of heliotrope on the boundary fence Lepidoptera new to the Isle of Wight in 2006 2006 was the best year in living memory for rare moths on the Isle of Wight with one species new to Britain, three new County records and five new vice-county records. These were as follows: New to Britain: Aedia leucomelas (L.). Totland, 11 September 2006 (Sam KoilLJones), New county records (Hampshire and the Isle of Wight): Antichloris eriphia (Fabr.) Dave Dana, found pupae on Columbian bananas at Morrisons, Lake, 5 February 2006. Dysgonia algira (L.) Totland, 12 September 2006 (Sam Knill- Jones). Proxenus (Athetis) hospes (Freyer) Bonchurch, 19 August 2006 (James Halsey). 68 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 New Vice-county Records (Isle of Wight, VC 10): Sophronia semicostella (Hb.) Totland, 24 June 2006 (Sam Knill-Jones). Cochylis molliculana (Zell.) Parkhurst, 5 August 2006 (Tim Norris & Sam Knill- Jones). Catoptria verellus (Zinck.) Bonchurch, 13 July 2006 (James Halsey). Nociua janthina (Borkh.) Bonchurch, 26 July 2006 (James Halsey). Coleophora albidella (D.& S.) Ningwood Common, one case found, 5 August 2006 (Tim Norris). — Sam Knill-Jones, 1 Moorside, Moons Hill, Totland, Isle of Wight P039 OHU. I married a Moth Man - a warning to new moth spouses With a few notable exceptions - Mary Harrap and Sarah Bradley spring to mind - moth people are male. I think it’s a collecting thing. As a child it was always the boys who climbed trees in search of birds’ eggs or who had albums of cigarette cards. And I would venture to suggest that the women’s involvement remains at interest level, stopping short of obsession. Over the years I have met many moth men and realised quite early on that they are all different, both from each other and from the rest of the human race. Some might even say, well, a bit......um, no, ITl stick with ‘different’. Over thirty years ago, when my husband Peter started collecting moths, after a lifelong interest, his mentor was a friend and colleague, Tim Peet, a surgeon. I was an anaesthetic nurse and many’s the time that Tim would come into the anaesthetic room with: “Tell Peter to look out for...” and proceed to sketch the characteristic features of some moth on the back of the patient’s notes. I sometimes wonder how subsequent surgeons might try to interpret those jottings in relation to the patient’s current medical condition. Tim gave Peter his first setting boards, pins and papers, taught him to set moths and we were off. A moth trap was bought together with a cabinet. Moth books, moth courses, moth societies ensued and more moth men. I forget how Peter first made contact with David Wedd but I met him before Peter did. Peter was away from Guernsey on a moth course - where else - and had arranged for David to set his moth trap in our garden. I would switch it on each evening and David would come each morning to empty it. This wasn’t the only trap he had with him. Remember how there used to competitions to fit as many people as possible into a Mini. With David, it was moth traps in a Nissan Micra. On about day three, I asked David if he would like to see Peter’s collection. I’ll swear there was a white trail left in the air- you know, the sort the cartoonist draws behind Tom when he’s chasing Jerry. He disappeared into the moth room ( yes, moth room - more ofthat below) to emerge a good hour later. Moth men do love looking at each other’s collections, a procedure which, as in this case, is NOTES 69 accompanied by much grunting, gasps of envy and some shaking of the head and, “I’m not sure about that one” - a polite way of saying “ he’s got that one wrong David, now a much loved friend, has emigrated to Alderney where his traps are a danger to shipping. Then came Phil Sterling. Phil is a micro man and should come with a hazard warning. You see, they all begin with macro moths, but in seemingly no time at all they become interested in the tiny ones. This means: smaller boards; smaller pins; smaller instruments; more books; another cabinet; and ...a microscope. Oh, and more space for all this. Few of these moths have common names and many are notoriously difficult to identify. Which is where Phil comes in. He identifies them. So, whenever he comes to stay, other moth men arrive with (lots of ) boxes of specimens for him to look at. The problem is, that not all can be identified by just examining the whole moth. No, the only way to separate some moths is by examining their genitalia, which have to be dissected, put on a slide and examined under a microscope This applies to some of the macros too, and for them and some of the larger micros the original microscope will suffice. But problems arise as the moths get smaller, together with their diagnostic characteristics. There is a moth in the house as I write, which is barely visible to the naked eye and can only be separated from its look-alike by counting the protuberances on the inside of its aedeagus (penis - sort of) which has to be turned inside out! Yes, really. This means only one thing: another microscope. And more space for it ... and the slide cabinet, the water bath (if you don’t want him boiling up bodies on the cooker), a cupboard for the chemicals needed to produce the slide, even smaller instruments and more books of course. There are actually books containing nothing but pictures of moth genitalia. You can probably see now how things begin at a table in the dining room, move to a larger table in the spare room and culminate in a dedicated moth room. One day a parcel of sputum pots arrived in the post. They hadn’t been sent by the hospital but had come from another moth friend called Mike Dockery whom Peter had met on a moth course (of course ). The pots were subsequently returned over the next few months, each containing a Large Yellow Underwing. These were material for Mike’s PhD. His thesis was something to do with whether the moths rested with the right wing over the left or vice versa. Seriously. There are many, many more of these men, some of whom I’ve spoken to on the phone, some I know only by name. Like David Brown who runs moth courses. Peter has been on just twelve of them so far. There’s Shane from Stockport who has set up a genitalia mailing list and another Peter who is a meteorologist, and, when migrant moths land on these shores, tracks back from whence they came. They love migrant moths and, following a migration, the Internet fairly buzzes with first sightings, most northerly sightings, largest numbers etc. The first record is the most important of all. There is nothing quite like the first record of a moth. A migrant will do but a resident is better. First ever in the country is best of all, apart from that holy grail that all moth men seek: a moth that is new to science. 70 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 The thing is, after a while, it all becomes normal and it’s only when you talk about what your husband does in his spare time and see the incredulity on the faces of work colleagues and others outside this moth world that you remember just how strange it is. Guidelines on what to expect and how to survive • Buy him his own fridge. It’s not just that he fills yours with moth pots, but they tend to have bits of grass and bird dirt on them. • Put up extra book shelves. Although the Internet has reduced the need somewhat, books are still necessary. As a rule of thumb, the smaller the moth, the more expensive the book and the rate of price increase is exponential. Ditto microscopes. • If you don’t want him to empty the trap in the kitchen, consider giving him the garden shed, or, better still, a shed of his own. Choose the size carefully. Sometimes there will be other moth people in there with him. We have a moth shed at the end of the garden masquerading as a summer house. It’s full of moth traps - four at the moment, though he’s talking of another. The veranda has a variety of pots containing the foodplants of various moths. There is even a tub of sand with a large willow log stuck in it. Something to do with Phil Sterling. » Be prepared to accommodate lots of foodplants in the garden. I’ve got tansy in case the Tansy Pug should pass by, masses of Nicotiana for the Convolvulus Hawk, thrift for Thrift Clearwings .... The list is endless. • Learn to keep watch while he searches ladies’ lavatories. They seem to attract the best specimens. • Keep moth pots on every window sill. » Next time you re-carpet the guest room, choose a flecked pattern. This will disguise the detritus - leaves, twigs, moth wings etc. that drops off moth friends when they come to stay. • Accept that you will have to feed and care for caterpillars from time to time. I was once left with some that only ate the tops of gone - to - seed lettuces. I well remember tramping through fields with a sympathetic vegetable grower in search of some. • Be aware that you will develop a vicarious interest in all this. I never garden or go out for a walk without a moth pot in my pocket now. I have two colonies of moths. One is of the case-bearing (don’t ask ~ you’ll soon find out ) Clothes Moth which starts life under a bookcase in the games room and works its way up to the ceiling. The other is of Cosmopterix pulchrimella on a clump of Pellitory round the back of the house where I found the first pupa in our garden, and potted the first moth in Guernsey, while Peter and Phil Sterling were down at one of the bays searching for it. I have to admit to a certain degree of satisfaction that it was a ‘first’, the same satisfaction that I feel in being able to find the pretty little Yellow V-moth in almost any room in the house at the moment and knowing that very few people Britain have ever seen it. NOTES 71 I wonder if it’s worth setting up a moth spouses’ mailing list. I’ll ask Julia Peet, Carole Sterling, Dot Agassiz ... — Pat Costen, La Broderie, La Claire Mare, St Peters, Guernsey, GY7 9QA (E-mail: patcosten@cwgsy.net). Scythris potentillella (Zeller) (Lep.: Scythrididae) new to Hertfordshire During September 2005, my son Conall and I were searching for micros on Croxley Common Moor (VC 20: Hertfordshire; O. S. grid reference TQ 0894). The silken larval galleries of the gelechiid Teleiopsis dijfinis (Haw.) were found to be very common indeed as indeed were adults - sweeping Rumex acetosella typically producing a dozen or more specimens, with the highest density occurring among Rumex growing around mounds of rabbit droppings. Around a very few of these mounds, and restricted to perhaps a hundred square metres of this eastern part of the moor, we began unexpectedly sweeping specimens of a Scythris species. Each mound produced five or six specimens, along with many Teleiopsis and both species were seen to be resting on Rumex stems close to the ground. We subsequently ran actinic light traps here and both Scythris and Teleiopsis were attracted in abundance, our last sighting of Scythris being on 12 October with Teleiopsis persisting into November in small numbers. There was considerable variation in the overall appearance of the Scythris specimens and they were, initially, taken by me to include more than one species. The ground colour varied from dull metallic purple/brown to dull grey/brown with various patches of light grey scaling, mostly sub-apically on the forewing costa and/or halfway along the hind margin. Twelve specimens were subsequently dissected and ail proved to be potentillella; the identifications were kindly confirmed by Colin Plant who dissected a further two himself. Dr Paul Sokoloff also identified two specimens. Frequent visits to the moor during 2006 produced the first potentillella on 10 June, but then no more until 1 July, when two were found. Both potentillella and Teleiopsis diffinis (first seen during March) have been present in very reduced numbers during 2006, compared with 2005, with the last sighting of potentillella being on 23 September. While both species appear to have suffered a population crash between 2005 and 2006 other species which were common during 2005 have hardly been seen at all, notably Agonopterix subpropinquella (Stt.). These observations may prove interesting as Scythris potentillella is a new species for Hertfordshire (Colin Plant, pers. comm.), and one of rather few reliable records nationally. The observation that its numbers have been seen to fluctuate with those of Teleiopsis diffinis and that both are Rumex acetosella feeders, may also be of interest. I should like to thank both Colin Plant and Dr Paul Sokoloff for confirming the identity of 5. potentillella. — David Murray, Flat 2, 52 Marlborough Rd., Watford, Hertfordshire WD18 OQB. 72 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 Pale Shining Brown Folia bombycina (Hufn.) (Lep.: Noctuidae) re-discovered in Oxfordshire in 2005 and 2006 - a nationally signiOcant population of a UK Biodiversity Action Plan Priority Species Between 19 June and 15 July 2006, a total of 88 examples of Pale Shining Brown Folia bombycina were caught in 6 watt actinic light traps set in arable field margins on four farms in the area between Witney, Long Hanborough and Charlbury in west Oxfordshire. These were operated as part of sampling for a research project investigating macro-moth diversity in farmland (part of WildCRU’s Upper Thames Project - see below). The highest total in one night was 57 individuals (in three traps) and the peak appeared to be in the last few days of June and the first few days of July. In addition, two were caught in a Rothamsted Insect Survey light trap, operated as part of the same project near Hailey some 3 km north of Witney - one on 2 July and one on 7 July 2006. Previously, a single example was caught at MV light near Great Rollright, some 3 km north of Chipping Norton in Oxfordshire on 9 July 2005 by Andrew Turner, who trapped three at the same site together with Tony Davis on 30 June 2006. A further example was trapped at MV light in a garden in Over Norton, roughly 1km north of Chipping Norton, by Adrian Buckel on 3 July 2006. Folia bombycina has undergone a massive decline in Britain since the mid-1970s. Its current status is Notable B (Nationally Scarce), but it now probably merits Red Data Book status (thought to occur in fifteen or fewer 10 km squares). Until the mid- 1970s, it was widely and well distributed in southern and south-east England northwards to a line between the River Severn and the Wash (Waring et al., 2003: Field guide to the moths of Great Britain and Ireland. British Wildlife Publishing). Since 2000, the vast majority of sightings have been from Salisbury Plain, Wiltshire where it is recorded annually, but the population is thought to be small {Butterfly Conservation Lepidoptera Conservation Bulletin 7:15). Very few have been seen elsewhere, with very small numbers from other sites in Wiltshire, Norfolk and Hertfordshire. The Oxfordshire population appears therefore to be the strongest currently known in Britain. Before 2005, it was last seen in the county in 1984 and was widespread if local up to at least 1979 (Waring, 2002: Ent. Rec. 14: 128-129). Before its decline, P. bombycina was most common on light or calcareous soils (Heath & Emmet, 1979: The moths and butterflies of Great Britain and Ireland Vol. 9. Harley Books). The habitat in the area where the overwhelming majority of moths were caught in 2006 is open, largely arable farmland with generally low hedges and sparse trees, on rather thin, well-drained calcareous soil on limestone. The topography is rather flat and the land is relatively elevated (c. 100- 120m) so the climate is probably quite cold compared to more low-lying areas such as central Oxfordshire. There are quite large blocks of mixed and broadleaved woodland, mainly to the north. The field in which 57 were trapped in one night is almost adjacent to one of these, and has tall hedges and 6m wide grassy margins. However, most fields in the area have narrow l-2m wide margins. There is very little other semi-natural habitat. Each farm was sampled (along with a number of other farms, some in other parts of Oxfordshire) once during fortnightly periods from May to October, and 2006 was the first year of sampling at these sites. Consequently, the data gathered so far are NOTES 73 too limited to draw any conclusions concerning relative abundance at the different sites, or habitat associations. The main site near Chipping Norton is the Pauline Flick Reserve run by Banbury Ornithological Society, a stretch of disused railway line managed for conservation with tall scrub and open, sheltered grassy areas. Like the farm sites, it is on well-drained calcareous soil and is at a similar elevation. There are small blocks of woodland in the area and hedges are variable in size, some forming tall shelterbelts. There is also an apparently lightly managed grassy hillside 200m to the north. The topography is different, as this is quite deeply undulating countryside. The Over Norton garden site is on the edge of this area, with a large area of parkland nearby. It is interesting and perhaps rather surprising that such a population had apparently gone unnoticed, but the area has been very little recorded until recently and traditionally, arable farmland is not a habitat that greatly attracts the attentions of entomologists. The two areas in which the moth has been found in Oxfordshire are roughly 14 km apart. The terrain is essentially similar in the intervening area, and similar habitat extends across a large area of west Oxfordshire, adjacent parts of Gloucestershire including the Cotswolds, and just into Warwickshire, Some of these areas are undoubtedly under-recorded. It therefore seems likely that the moth occurs over a wide area, although recent experiences elsewhere suggest that if this is so, it may now be very localised within it. In Gloucestershire, there are a cluster of records northeast of Cheltenham from the early 1990s, with one further east towards Stow- on-the-Wold, The last county record is from 1996 (Gaunt, 2006: Gloucestershire moths - a second account. Published privately). Recent trapping in parts of Warwickshire adjacent to the Chipping Norton area has failed to produce the moth. This included two sessions at an apparently suitable site 6km away from the Great Rollright site, at the right time of year and in good conditions with multiple MV light traps (David Brown, pers. comm.). Records for Warwickshire are concentrated in the south of the county, with the last in 1995 from Bidford-on-Avon, where it had been recorded fairly regularly since 1984 (Brown, 2006: The larger moths of Warwickshire. Atropos Books). The terrain is somewhat different in most of south Warwickshire, being more low-lying and generally less calcareous, and therefore somewhat dissimilar to areas which the moth seems to prefer. Therefore, the evidence tentatively suggests that Great Rollright may be near its current northerly limit in this part of the south Midlands. However, until more is known of the ecological requirements of this moth, we can only speculate on its likely distribution. The larva has not been found in the wild (Waring et al op. cit.), in spite of intensive searches at known sites in recent years, in particular Salisbury Plain (Tony Davis, pers. comm.) and a search in autumn 2006 at one of the Oxfordshire farms. The larvae feed on a variety of herbaceous plants in captivity, as well as woody species such as willows and Common Hawthorn. They are not recorded feeding on grasses. Larvae obtained from a female captured in Oxfordshire in 2006 accepted Dandelion, Broad-leaved Dock and Common Hawthorn, being particularly keen on the former. It seems likely that woody species are generally only eaten in the spring, when their leaves are more easily digested. 74 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 Those given only hawthorn in autumn 2006 remained healthy, but their growth was very slow. The larvae are highly negatively phototaxic and rapidly hide under tissue or soil if brought into the light. Therefore, we speculate that in addition to being nocturnal in the wild, they might only be active well after dark and perhaps only on darker nights. Whilst the overwintering stage of the genus Polia is normally the larva (Ronkay, Hacker & Hreblay, 2002: Noctuidae Europaeae Vol. IV Hadeninae /. Entomological Press, Sor0), the overwintering stage of R bombycina seems unknown since all successful rearing attempts of which we are aware have been by forcing. The larvae reared by MCT at room temperature in 2006 fed up steadily and pupated to emerge in late October or November. Some kept in an unheated outhouse only reached about half grown (penultimate instar) and stopped growing. These were put outside on potted plants, but have probably not survived. It probably overwinters as a small larva. It is hoped that the discovery of an apparently strong population of this moth will present the opportunity to learn something of its ecology. Further work will concentrate on continued monitoring, searches for larvae, more intensive light trapping with a mark-release experiment, light trapping over a wider area and further captive breeding in natural conditions with behavioural observations. The Upper Thames Project is a collaborative research project led by the Wildlife Conservation Research Unit (WildCRU), Department of Zoology, Oxford University investigating the effects on diversity of the management of lowland farms, with an emphasis on declining species. The moth work is funded by the Esmee Fairbairn Foundation within a wider framework funded by the Tubney Trust, and is in partnership with Butterfly Conservation. We are grateful to Rothamsted Research for their support. We would like to thank Tony Davis and Mark Parsons (Butterfly Conservation), Ruth Feber and David MacDonald (WildCRU), Martin Corley, Andrew Turner, Adrian Buckel, Juliet Hopwood (Rothamsted light trap operator), David Brown (Warwickshire Moth Recorder), Roger Gaunt (Gloucestershire Moth Recorder), Norman Hall and Thames Valley Environmental Records Centre for comments and information in the preparation of this note, and the farmers for allowing us access to their land. — Martin C. Townsend and Thomas Merckx, Wildlife Conservation Research Unit, Department of Zoology, University of Oxford, Tubney House, Abingdon Road, Tubney, Oxfordshire, 0X13 SQL (E-mails: martin.townsend4@ntlworld.com and thomas.merckx@zoo.ox.ac.uk). Diaperis boleti (L.) (Col.: Tenebrionidae) in Hatfield Forest, Essex Diaperis boleti is an unusual darkling beetle that eats and tunnels into the polypore fungus Piptoporus betulinus, commonly seen growing on the trunks of dead and dying birch trees Betula spp.. Traditionally, this has been a rare beetle in the UK, but in recent years the incidence of finding has increased, especially on the eastern sideof the UK. In June of 2006, during a visit to Hatfield Forest in North Essex, the reachable P. betulinus on two dead birch trees were tapped with a stick above a beating tray. From the fungi on the first tree, nine adult D. boleti fell onto the beating tray. From the second dead birch, one bracket of polypore yielded no less than 15 adult D. boleti. Within the confines of Hatfield Forest there are many dead, standing NOTES 75 birch trees infested with polypore, but they are very patchily distributed and quite difficult to find, however the beetle must be very sensitive to the volatile odours produced by this fungi or the characteristic scent of birch wood attacked by this saprophyte. — Ross Piper, 17 Southmill Court, Southmill Road, Bishop’s Stortford, Hertfordshire CM23 3DA (E-mail: ross_piper@yahoo.com). Editorial Comment: It may be of interest that the late Charles Watson reared a large number of Diaperis boleti from a single Piptoporus betulinus bracket collected on 1 January 2002 from a dead silver birch tree at Wall Wood, a satellite woodland of Hatfield Forest. The fungus was kept in his garage and the adults emerged in the first few days of November 2002; two specimens are now in my collection. Red Admiral Vanessa atalanta (L,) (Lep.: Nmyphaiidae) courtship in winter The Red Admiral butterfly is having an extraordinary time in Britain at present. Its annual abundance has increased spectacularly since the mid-1970s (Fox, R. et al 2006. The State of Butterflies in Britain and Ireland. Pisces Publications, Newbury) and, over the same period, the number of winter sightings has risen from a negligible level to the Red Admiral being the most frequently encountered butterfly in winter (Bowles, N. and Fox, R. 2006 British Wildlife 17: 280-282). The winter of 2006/07 proved no exception with Red Admiral records received from over a dozen counties on New Year’s Day 2007 alone (Nick Bowles pers. comm.). The current consensus is that such sightings represent over-wintering butterflies rather than recently arrived immigrants (Burton, J. 2007 Atropos 29: 3-11). Larval activity, growth and survival during the winter months have also been noted with increasing frequency in recent years (Asher, J. et al. 2001. The Millennium Atlas of Butterflies in Britain and Ireland. OUP, Oxford). It appears that the Red Admiral is (perhaps not for the first time) making the transition from being a migrant summer-breeding species in Britain to a year-round resident. Interwoven with this shift in the status of the Red Admiral are apparent changes in the species’ behaviour, at least in the autumn and winter. Male territorial behaviour, for example, has been observed recently during autumn; a season when male Red Admirals might otherwise be expected to be either migrating southwards or feeding up for overwintering (Dennis, R.L.H. et al. 2006 Entomologist's Gazette 57: 83-89). Territorial behaviour by males suggests that some Red Admirals are breeding in Britain during the autumn. As recently as 1997, M. Tucker stated that “hardly anyone has seen a paired couple of Red Admirals in the wild in the British Isles and observations of genuine courtship behaviour between males and females are almost as scarce” (The Red Admiral Butterfly. Butterfly Conservation, Dedham, Essex). He could cite only one record (in 1984) of Red Admirals mating in Britain. Over the last decade however, there have been another seven reports, including a pair that I was fortunate to observe myself (Fox, R. and Sleep, T. 2005 Atropos 25: 66-67). On 14 January 2007, I observed two Red Admiral butterflies engaged in what appeared to be courtship behaviour at Stover Country Park (SX 833751), nearNewton Abbot, Devon. The two butterflies were flying very close together, one behind the other, at about 2m height around a sunny woodland edge. Their flight was 76 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 slow and did not involve any clashes between the individuals or the upward spiralling flights that characterise aggressive encounters between males. The butterflies alighted briefly on tree foliage but almost immediately resumed their leisurely flight. Although they were only in view for about a minute, and I was not able to ascertain the sexes of the butterflies involved, the observation corresponds closely with described courtship behaviour. It would be of great interest to hear from other observers who have witnessed such behaviour during the winter months. Although extraordinary for Britain, all of these recent observations reflect the normal pattern of winter activity for the Red Admiral in southern Europe (Stefanescu, C. 2001 Ecological Entomology 26: 525-536) and the formation of permanent British Red Admiral populations in response to climate change was predicted (Dennis, R.L.H. 1993. Butterflies and Climate Change. Manchester University Press, Manchester). Nevertheless, courtship in mid-January represents a remarkable development in the dramatic recent history of the Red Admiral in Britain. — Richard Fox, Butterfly Conservation, Manor Yard, East Lulworth, Dorset BH20 5QP (E-mail: rfox@butterfly-conservation.org). Atlantopsocus adustus (Hagen) (Psoc.: Psocidae) new to Britain from East Cornwall While surveying the coastal land east of the Fowey River in East Cornwall in August 2006 some large barkflies were retained for checking. They appeared to be an Amphigerontia species when netted, but proved to be an Atlantopsocus when taken through the new identification key (New, 2006. Handbk Ident. Br. Insects 1 (7)). Only A. personatus is covered by New (2006) although it has never been found in Britain - he comments that reports of its incidence in southern England have yet to be confirmed. It is best known in Ireland where it appears to be widespread. The wings of A. personatus are however un-spotted apart from the pterostigma, and the two female specimens which had been retained had noticeable dark markings on the wings - similar to an Amphigerontia. The specimens were accordingly sent to Bob Saville for his opinion, but he was equally puzzled and sent them on to Charles Lienhard who has now determined them as Atlantopsocus adustus and new to the British List. A. adustus is only otherwise known from Madeira and the Canary Islands where it has been found on various trees and shrubs. It can be identified using Lienhard (1998 Psocopteres Euro-Mediterraneens. Eaune de France 83). The specimens had been knocked from the lower canopy of Cornish elm Ulmus minor and alder Alnus glutinosa growing along a streamside Cornish hedge in a small coastal valley near Palace Cove in Lantivet Bay, Lanteglos (SX161512), 26.viii.2006, together with Elipsocus hyalinus (Stephens), E. pusillus Lienhard and Valenzuela flavidus (Stephens). Thanks to Bob Saville and Charles Lienhard for helping with the identification of the specimens and to Spalding Associates for contracting the author to carry out the survey. The land is owned by the National Trust. — Keith N. A. Alexander, 59 Sweetbrier Lane, Heavitree, Exeter EXl 3AQ (Email: keith.alexander@waitrose.com). NINETA PALLIDA NEW TO BRITAIN 77 NINETA PALLIDA (SCHNEIDER, 1846) (NEU.: CHRYSOPIDAE), A LACEWING NEW TO THE BRITISH ISLES ‘ Martin C. Harvey and ^ Colin W. Plant ' Buckinghamshire and Milton Keynes Environmental Records Centre, Tring Road, Halton, Aylesbury HP22 5PN (email: mcharvey@buckscc.gov.uk) ^ 14 West Road, Bishops Stortford, Hertfordshire CM23 3QP (email: cpaukl @ ntlworld.com) Abstract The discovery of Nineta pallida (Schneider, 1846) (Neuroptera: Chrysopidae) in Britain is reported and discussed. A revised key to the identification of adult Nineta species is presented along with drawings of the male terminalia. Introduction On the night of 23 September 2006, MCH organised a moth recording evening at Wendover Woods, in the Buckinghamshire Chilterns, at O. S. grid reference SP 88980886, for UK National Moth Night. Amongst the non-lepidopteran insects seen was a large green lacewing which MCH recognised as belonging to the genus Nineta. However, upon closer inspection it became apparent that it did not match any of the three known British Nineta species described in Plant (1997). It came nearest to Nineta inpunctata (Reuter 1894), which has only recently been found in Britain and remains known here from a single specimen (Plant, 1996). However, the long veins of the wing are green and the dorso-lateral aspect of the thorax bears-reddish brown stripes; the Wendover specimen was clearly not inpunctata. The specimen was passed to CWP who recognised it as Nineta pallida, an apparently very localised European species associated with spruce Picea spp. and not previously found in Britain. Since this species was unexpected in Britain, CWP sent the specimen to Dr Herbert Holzel in Austria, who confirmed the identification. Details of the record Wendover Woods is a large (325 hectare) area of mixed woodland, managed by the Forestry Commission, rising to approximately 260 metres above sea level in the south of England. Norway Spruce Picea abies covers about 13% of the woodland area, some of it managed for the production of Christmas trees; in fact the area of Christmas trees nearest the point of capture for N. pallida was harvested in autumn 2006 and is being restored to grassland (Jo Mason, Forestry Commission. Pers. comm.). The capture site was in a thin belt of young woodland containing a mix of Oak Quercus robur. Beech Fagus sylvatica, Birch Betula sp.. Larch Larix europaea and Norway Spruce. This area of the woodland is near to the main car park and cafe of this popular site, with hundreds of visitors every weekend. The insect is a female and was found on the trunk of a Larch tree next to, but not actually on, a wine-rope that had been put up to attract Lepidoptera and other insects. A mercury- vapour light was running in a clearing a few metres away. 78 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 According to local weather stations in Buckinghamshire, the weather on 23 September 2006 was generally mild (minimum 12°C.) with low winds from the south-east, but the sample location was quite exposed, and felt cool and breezy. Distribution in Europe Aspock et al. (1980) gave a distribution map for Nineta pallida in Europe, and at that time it was confined to the central European region in Austria, Germany, Switzerland, Czech Republic, Hungary, Poland, Romania and Slovenia with a single station in the extreme south-east of France. The Fauna Europaea website at www.faunaeuKorg, managed by Aspock and Miillan lists the insect in these countries and adds Italy, Spain and the Ukraine. In addition to this there are recently published records for Belgium (Bozsik et al., 2002), Denmark (Popov, 2002) and Turkey (Canbulat and Kiyak, 2002). In France, Canard et al. (2006), indicate that the insect is now present in Vosges (Lorraine), Doubs and Jura (Franche-Comte) and Ain (Rhone-Alpes) in the east and has recently spread south-westwards, to the Lozere (Languedoc) and the Ariege, Haute-Garonne, Gers and Hautes-Pyrenees Departements in the Midi-Pyrenees Region. Thus, the lacewing has clearly spread in several directions from its central European origins. With this in mind, its presence in Britain was perhaps predictable and our initial surprise that this first British record should occur so far inland, over 100 km from the coast, is diminished by knowledge of the leap-frogging that has gone on between French Departements. Ecology N. pallida is associated with Spruce in forests, both as an adult and a larva (Popov, 2002) and is found principally in the tree canopy layer (Szentkiralyi and Kristin, 2002). As already mentioned, Norway Spruce covers about 13% of the woodland area at Wendover and significantly there has not been any recent importation to this site of spruce trees or other forestry materials from the continent (Jo Mason, Forestry Commission, pers. comm.). Presumably the larvae prey on aphids in the canopy, such as the Green Spruce Aphid Elatobium abietinum (Walker). Nineta pallida has generally been considered an insect of high altitudes (e.g., Czechowska, 2002). Canbulat and Kiyak (2002) state that it can be found among Spruce in mountain forests, waterlogged forests and higher- altitude planted monocultures. However, some of the more recent records from the continent have been at lower altitudes, perhaps indicating that the species is adapting to new conditions. The Belgian specimen was collected by sweep-netting in the vicinity of Gembloux Agricultural University in July 1997, a lowland area containing gardens, parks and a nature reserve (Bozsik et al. 2002). The Turkish specimens, a male and a female, were collected from Corsican Pine Pinus nigra (using a “net trap”) on 23 August 2001 (Canbulat and Kiyak, 2002). In Slovakia the adult flight period includes May- July (Szentkiralyi and Kristin, 2002). The species overwinters as a first-instar larva, and there is one generation per year, with the adults perhaps aestivating under some circumstances (Michel Canard, pers. comm.). NINETA PALLIDA NEW TO BRITAIN 79 Identification Seven species of Nineta are currently recognised as occurring in Europe, although there is a division of opinion concerning the status of N. principiae, which is regarded by some as a subspecies of N. guadarramensis. With four of these now known to be present in Britain, it seems sensible to present a key to all the species rather than just the four already recorded here. Plant (1997) provides a key to species within the Chrysopidae. In that work, Nineta vittata (Wesmael) runs out at couplet 15, on the basis of its distinctive elongated antennal scapes. The following modification to couplet 17 of the key should enable N. pallida and the remaining European species to be distinguished. Characters in bold are critical; non-bold characters are supporting features. Illustrations of the male terminalia are also provided (Figs. 1 - 7) for all seven species. These illustrations were most kindly supplied by Michel Canard and first published in Canard et al. (1998). 17 Costal margin of fore wing concave (This character may be less 17a obvious in females, and it is recommended that a straight edge be placed along the costa to aid interpretation). Costal margin of fore wing not concave 17b 17a Costal cross- veins of fore wings more or less entirely pale, rarely darkened. Cilia in the basal fifth (nearest the body) pale and relatively long and thin, at least as long as the width of the costa and sometimes longer than this width. Hairs on the front face of the front coxae pale, long and fine. Costal cross-veins of fore wings more or less entirely darkened or at least darkened at the ends. [Non-British species.] N. flava N. guadarramensis and N. principiae 17b Pseudo-median and other long veins of fore wings (radial sector N. pallida and pseudo-cubital) green. Costal cross veins of fore wings green. Upper surface of thorax usually with reddish brown bands (may fade, especially in alcohol). Pseudo-median vein of fore wing black (or at least darkened 17c compared to the cross-veins). Upper surface of thorax green and yellow - never with reddish brown markings. 17c Costal cross veins of fore wings darkened. In the fore wing, the N. inpunctata radial sector and the zig-zag longitudinal vein in the space between the radial sector and the pseudo-median vein converge towards the wing tip. Cilia in the basal fifth of the costa of the fore wing black, short and stout, scarcely longer than the width of the costa. Hairs on the front face of the front coxae short, stout and black. [If the specimen does not quite fit, check that it is not an un- spotted form of Chrysopa pallens (= septempunctata)] . Costal cross veins of fore wings green - not darkened. In the N. carinthiaca fore wing, the radial sector and the zig-zag longitudinal vein in the space between the radial sector and the pseudo-median vein do not converge, but run more or less parallel to each other all the way to the wing tip. [Non-British species.] 80 ENTOMOLOGIST’S RECORD, VOL. 119 25.iii.2007 7. N. vittata (Wesmael) NINETA PALLIDA NEW TO BRITAIN 8i Discussion The spread of insects traditionally regarded as being more or less sedentary is a phenomenon that is becoming increasingly common. Links have inevitably been made with recent changes in overall planetary climate and whether these changes prove to be long or short term it is likely that they will stimulate further range alterations amongst European insects. The discovery of Nineta pallida in Britain, hot on the heels of its congener N. inpunctata (Plant, 1996), serves as a salutary reminder that any specimen that “does not quite fit the key” should be subjected to a critical examination by a person with experience of the group in a wider geographical context. Plate D. Nineta pallida (Schneider), Wendover Wood, Buckinghamshire, 23.ix.2006. Leg. M.C. Harvey. (Photograph by C. W. Plant) Facing page: Figs. 1-7. Male terminalia of European Nineta species. Abdomens are aligned with the insects’ heads to the right. Drawings copyright © Michel Canard (Toulouse). 82 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 Acknowledgements We are most grateful to Dr Herbert Holzel (Brtickl, Austria) for confirming CWP’s initial identification of the Wendover specimen and for providing us with information on its distribution. CWP also wishes to record particular gratitude to Dr Michel Canard (Toulouse, France) for permission to reproduce the drawings of male genitalia of European species that originally appeared in Canard et al (1998) and for kindly providing us with the original drawings for reproduction. MCH records thanks to the Forestry Commission for permission to record insects at Wendover Woods. References Aspock, H., Aspock, U., and Holzel, H., 1980. Die Neuropteren Europas. Vol. I, 495 pp., Vol. 11. , 355 pp. Goecke & Evers, Krefeld. Bozsik, A., Mignon, J. and Gaspar, C.H., 2002. The green lacewings in Belgium (Neuroptera: Chrysopidae). Acta Zoologica Academiae Scientiarum Hungaricae 48 {SuppL 2): 53-59. Canard, M., Cloupeau, R. & Leraut, R, 1998. Les Chrysopes du genre Nineta en France. Bulletin de la Societe entomologique de France 103 (4): 327 - 336. Canard, M., Mazel, R. & Thierry, D., 2006. Repartition des Chrysopes en France (Neuroptera, Chrysopidae). Bulletin de la Societe entomologique de France 111 (3): 353 - 366. Canbulat, S. and Kiyak, S., 2002. Nineta pallida (Schneider, 1846) new to Turkey (Neuroptera: Chrysopidae). Journal of the Entomological Research Society 4(1): 1 1-14. Czechowska, W., 2002. Raphidioptera and Neuroptera (Neuropterida) of the canopy in montane, upland and lowland fir forests of Abies alba Mill, in Poland. Fragmenta faunistica 45:31-56. Plant, C. W., 1996. Nineta inpunctata (Reuter, 1894) (Neuroptera: Chrysopidae): a green lacewing new to Britain. Entomologist’s Gazette 47(2): 115-120. -, 1997. A key to the adults of British lacewings and their allies (Neuroptera, Megaloptera, Raphidiptera and Mecoptera). Field Studies Council, Preston Montford. Popov, A., 2002. Neuropterida of northern Europe. Acta Zoologica Academiae Scientiarum Hungaricae 48 (Suppl. 2): 281-291. Szentkiralyi, F. and Kristin, A., 2002. Lacewings and snakeflies (Neuroptera, Raphidioptera) as prey for bird nestlings in Slovakian forest habitats. Acta Zoologica Academiae Scientiarum Hungaricae 48 {Suppl. 2): 329-340. An invasion of the Harlequin Ladydird (Harmonia axyridis Pallas) (Col. Coccinellidae) in the South Wight A swarm of Harlequin Ladybirds Harmonia axyridis descended on the South Wight in the thousands in 2006. It is probably the first time such a mass has been observed in this country. Walkers along the Island’s south coast and on Compton Chine, bird watchers on Ventnor Down and householders in the Ventnor and Mottistone areas reported seeing thousands of these insects. I had one in the kitchen here on 6 November. In France, Belgium and Holland, their numbers are soaring annually. Sighting in Britain have been mainly restricted to the south-east, extending from Hampshire to Norfolk. — Sam Knill-Jones, 1 Moorside, Moons Hill, Totland, Isle of Wight P039 OHU. NOTES 83 A naturalised population of a Mediterranean earwig, Forficula pubescens Gene (Derm.: Forficulidae) in West Sussex On 13 September 2006 I visited a nursery that specialises in exotic plants to search for exotic insects. The nursery, near Ashington, West Sussex, holds stocks of trees and shrubs imported from France, Italy, Spain and elsewhere. By beating a tubbed Photonia fraseri, imported from the Netherlands, I soon found a small pale adult male earwig that I immediately recognised as Forficula pubescens Gene. Within a few minutes, a second example was obtained by beating a tubbed pine tree and two females and a male were obtained by beating hogweed in an overgrown patch of vegetation on the edge of the site. Clearly, the earwig was well established and had spread to a variety of plant species. I also found a large macrolabic specimen of Forficula auricularia (L.) by beating Pinus pinea that had been imported from France some months previously. Forficula pubescens occurs around the western Mediterranean (Caussanel and Albouy. 1990. Dermapteres (Perce-oreillesj Faune de France IS 1990; Herrera, 1999. Catalogue of the Dermaptera of Spain. Newbook Ediciones). I was able to confirm my field identification using (Harz and Kaltenbach, 1976. Die Orthopteren Europas III: The Orthoptera of Europe III. The Hague: Junk) and by comparison with specimens I collected at Salou, Tarragona, Spain in 1987. In Spain, I collected this species by using vegetable oil to flush specimens from the deep indentations of gnarled tree trunks. My guess is that the Sussex population originated from one or more examples imported on trees from Spain: there were several mature Spanish olive trees and palms of various kinds in tubs close to where the earwigs were found. Some of the olive trees had been outdoors at the nursery for three years. Using currently available keys to British Dermaptera, Forficula pubescens could be misidentified as Forficula lesnei Finot. Both species are of similar size and colour and early finds of F. lesnei in Britain (Burr, 1897. British Orthoptera (Earwigs, Grasshoppers and Crickets). Huddersfield: The Economic and Educational Museum) were erroneously attributed to Epubescens, but were later corrected to Flesnei (Lucas, 1920. A Monograph of the British Orthoptera. London: Ray Society; Burr, 1936. Britis/i Grasshoppers and their allies: A stimulus to their study. London: Philip Allan). Otherwise there do not appear to be any published records of F. pubescens from Britain, so this species may now be added to the British list as a naturalised alien. Adult male Forficula pubescens are easily identified by the distinctive shape of the cerci (Plate E). Compared with F. lesnei, the basal parts of the cerci are longer so that the paired basal parts together appear as a rectangle. In F. lesnei, each basal part is shorter, about twice as long as broad, so that together the basal parts form a roughly square shape. Also the dentition on the internal aspect of the basal parts differs: in F. pubescens there is a large tooth at the distal angle of each basal part plus other smaller teeth that are unevenly spaced along the internal aspect of the basal circus, whereas in F. lesnei the teeth are more evenly spaced. Females are less readily identified although there are differences in the shape of the elytra: in F. lesnei they are roughly square-ended while in F. pubescens the hind margin is obtusely angled (Caussanel and Albouy, op. cit.). Nevertheless, these differences are 84 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 subtle and it would be unwise to base records on females alone. Also, in Italy and the eastern Mediterranean there are additional species that could be confused with F. pubescens, although reference to the shape of the male cerci would allow identification (Harz and Kaltenbach, 1976. op. cit.). The current fashion for exotic and sculptural plants from southern Europe suggests that it is quite likely that F. pubescens has been introduced to parks and gardens across Britain. It is possible that it could become established, temporarily at least, in warmer coastal or urban areas. I thank Bruce Jordan for allowing and encouraging entomological investigation of the nursery.— John Paul, Downsflint, High Street, Upper Beeding, West Sussex BN44 3WN. Plate E. Forficula pubescens Gene. Ashington, West Sussex, 13.ix.2006. Photograph copyright © John Paul DIPTERA NEW TO IRELAND 85 RHAPHIUM NASUTUM (DIPTERA; DOLICHOPODIDAE), PHERBELLIA ROZKOSNYI & TETANOCERA MONTANA (DIR; SCIOMYZIDAE), INSECTS NEW TO IRELAND AND GEOMYZA BALACHOWSKI (DIR: OPOMYZIDAE), PRESENCE IN IRELAND CONFIRMED Martin C. D. Speight Department of Zoology, Trinity College, Dublin 2, Ireland. ( E-mail: speightm® gmail. com ) Abstract The species Pherbellia rozkosnyi, Rhaphium nasutum and Tetanocera montana are added to the Irish list of Diptera and the presence of Geomyza balachowski in Ireland is confirmed. Notes are provided on the identification of these species and their known biology. Points of potential biogeographical interest are discussed. Introduction The Diptera known from Ireland were listed by Chandler (1998). There do not appear to have been any additions to the Irish opomyzid list since then (but see below) and the only additional sciomyzid species for which Irish records have been published is Colobaea distincta (Ryder et al., 2003). There have been several additions to the Irish dolichopodid list since Chandler (1998) appeared, but Rhaphium nasutum (Fallen) is not among them. The present text provides first Irish records of one opomyzid species and two sciomyzid species, all of them collected during course of survey work conducted on a farm in Co. Cork. The general character of that farm, and its recent land-use history, are described by Good (2001). Geomyza halachowskyi Mesnil, 1934 Co. Cork: W6658 (NT2), Glinny, Riverstick; various dates between 9 August and 8 October 2005, males; Malaise traps; hay meadows and humid, disused, seasonally- flooded, unimproved Deschampsia/Molinia grassland; coll, and det. M.C.D. Speight; specimens deposited in collections of National Museum of Ireland. The confused nomenclatural history of this small fly is detailed by Drake (1993). Chandler (1998) cites the closely similar G. hackmani as occurring in Ireland, but not G. balachowskyi. Enquiries of Robert Nash, who maintains the Ulster Museum database listing Irish Diptera, reveal that there have apparently not been any subsequent published records of G. balachowskyi from Ireland (R. Nash, pers.comm.). However, the Fauna Europaea (FAEU) website (http://www.faunaeur.org) gives this species as “present” in Ireland. Unfortunately, FAEU gives no information on the source of its entries, so there is no way of knowing why it records G. balachowskyi from Ireland. There was no requirement of contributors to FAEU to cite species only from parts of Europe for which there were published records and it is thus possible that the FAEU citation of G. balachowskyi for Ireland is based on unpublished data. Whether this is so, or whether the citation is simply an error, cannot be determined. Whichever explanation is correct there is 86 ENTOMOLOGIST'S RECORD, VOL. 119 25Jii.2007 evidently need to validate the FAEU entry by reference to an actual occurrence of this species in Ireland, backed up by reference material. The present note hopefully serves that purpose. The male of G. balachowskyi can be determined using the key and figures of the male terminalia provided by Drake (1993). The female cannot reliably be separated from the female of G. hackmani. G. balachowskyi is known from most parts of Europe and is known in Britain from the Scottish Highlands to the south coast of England. There would seem no reason why it should not prove to be widely distributed in Ireland. Its larvae are believed to feed in stems of Arrhenatherum, Holcus and Lolium. According to Drake (1993) the flight period of this species is uncertain, because it has been so confused with G. hackmani. The Co. Cork specimens were all collected between August and October. G. hackmani was collected by the Malaise traps on the farm during the same period, and also earlier in the year (June/July). Pherbellia rozkosnyi Verbeke, 1967 Co. Cork: W6658 (NT2), Glinny, Riverstick; 1-20 September 2005, male; Malaise trap at edge of ditched stream, Alnus-Salix scrub/seasonally-flooded, unimproved, oligotrophic Molinia/Deschampsia grassland, coll, and det. M.C.D. Speight. Pherbellia rozkosnyi is a poorly-known species only reliably distinguished from the more-frequently encountered P. scutellaris by means of features of the male terminalia. Rozkosny (1991) clearly depicts the relevant differences, if in a rather diagrammatic form. The females of these two species still cannot be distinguished with confidence. P. rozkosnyi is known from Fennoscandia south to the Alps and from Britain eastwards through central Europe to Switzerland. Attention was first drawn to the presence of P. rozkosnyi in Britain by Perry (1990), who found it in ‘damp, shaded woodland’ in south west England (North Devon) and there are subsequent records from east and north east England (Suffolk, Durham) given by Cole (1997). The Suffolk record was from Betula/Quercus woodland on sandy soil and the Durham record from ‘a damp limestone gorge’ (Cole, 1997). The Malaise trap that collected the solitary Irish male specimen reported here was one of a series installed in various habitats on a farm. This particular trap was beside a ditch running along the edge of a seasonally-flooded, disused, unimproved, oligotrophic Deschampsia/Molinia grassland invaded by thickets of scrub Salix and Alnus, with wet, mature Alnus woodland on the other side of the ditch. Malaise trapping in the Alnus wood did not produce P. rozkosnyi but did produce a few specimens of the closely similar P. scutellaris. European data demonstrate that adults of P. rozkosnyi occur from June to September, with peaks towards the beginning and end of this period. The developmental stages of this species are unknown. Small sciomyzids, like species of Pherbellia, are not much susceptible to collection by Malaise trap and neither are they easy to collect using a sweep net, especially from tall, tussocky vegetation like the grassland that produced the P. rozkosnyi specimen reported on here. Work on sciomyzids in Ireland has not been sufficiently systematic or widespread to provide a basis for deciding whether P. DIPTERA NEW TO IRELAND 87 rozkosnyi is probably restricted to either the south west of the island or to some particular habitat type in Ireland. All that can be said is that there are no other Pherbellia species only known from one record in Ireland and that P. scutellaris, to which P rozkosnyi is closely similar, is not infrequently recorded. Now that both P. rozkosnyi and P. scutellaris are known to occur in Ireland any earlier records of P. scutellaris based only on females must be regarded as unreliable and care will be needed to check the terminalia of any males collected in future, if correct determination is to be ensured. Similarly, unless their terminalia have been checked, the identity of males in museum collections named as P scutellaris cannot be relied upon. Rhaphium nasutum (Fallen, 1823) Co.Cork: W6658 (NT2), Glinny, Riverstick; 20 July-9 August, 2005, male. Malaise trap in broad field margin of hay meadow, beside ditched seasonal stream backed by mature hedge of Rubus fruticosus/Prunus spinosa/Salix/Sambucus\ coll, and det. M.C.D. Speight; specimen deposited in collections of National Museum of Ireland. Rhaphium nasutum is a reasonably distinctive species - at least in the male - whose features are som.ewhat misleadingly represented in Fonseca (1978). The genital lamellae are not only bifurcate, with the two elements of each fork of unequal length, as mentioned by Fonseca (1978), but also very long and ribbon-like. In a fresh specimen these elements are quite straight and directed anteriorly, along the ventral surface of the abdomen. The most distinctive feature of the male fore tarsi is a blunt spike-like projection present apically, on the ventral surface of the second tarsomere. This projection, which is entirely missing in the rather similar species R. commune Mg., remains unmentioned by Fonseca (1978), but is reasonably clearly figured by Parent (1938) and Negrobov (1979). R. nasutum is a Holarctic species, in Europe known mostly from central and northern parts of the continent. In the Atlantic zone it appears to be generally infrequent and is included on at least one “Red List”. A.ccording to Pollet (2000) it is a species found along the margins of large bodies of standing water, or big rivers, but the existing literature is not very helpful in defining either macrohabitats or microhabitats with which R. nasutum is associated. Its developmental stages remain unknown. The closest water to the Malaise trap on which the present record is based is an almost-permanent (i.e. flow ceases in dry summers) small stream flowing along the bottom of a ditch that is approximately 1.5 metres deep, overshadowed by an adjacent hedge and carrying little vegetation on its sides or bottom. There are no large v^^ater bodies, standing or running, within many kilometres of the trap. The hayfield in which this Malaise trap was installed is humid, with sparse Juncus growing among the tall grasses, in particular along the field margin, but at no time of the year does the field carry areas of standing water. The ditch is clearly an active element of the farm landscape, in the immediate vicinity of the trap, demonstrably supporting the development of subaquatic species - emergence trapping carried out along its bottom produced the sciomyzid Renocera pallida, whose larvae predate pea mussels (populations of which are present just beneath the surface in the ditch- bottom) and the syrphids Chrysogaster solstitialis, Ripponensia splendens and 88 ENTOMOLOGIST’S RECORD, VOL. 119 25.iii.2007 Sphegina elegans (Speight, in litt.). None of these species could be expected to develop in the hayfield itself (and none of them were found in emergence traps installed on the hayfield margin). Through wave-action the margins of large water bodies can exhibit areas bare of vegetation and the margins of large rivers can likewise develop bare areas due to fluvial erosion processes. Perhaps R. nasutum has some association with such bare areas? The ditch on this farm would seem to have little in common with a large water body other than bare ground alongside water. Clearly better habitat information is needed for R. nasutum. But how much is known of the dolichopodid fauna of farmed land in general? While the limited resources available for inventorising insect faunas in Europe are understandably mostly focused on gaining a better understanding of nationally and internationally-important sites, for many taxonomic groups there remains little published information on the species than can be found in farmland or the circumstances under which those species survive. It remains possible for such species to persist in farmland undetected, simply due to a lack of work in the farmed landscape - see, for instance Helden and Sheridan (2006). If Rhaphium nasutum were to occur in association with unvegetated field ditches in many parts of Ireland this could certainly have gone undetected and unpredicted, given the limited attention that dolichopodids have received within farmland. Under these circumstances the status of R. nasutum in Ireland can only remain a matter for conjecture, until and unless farmland faunas become better known. Tetanocera montana Day, 1881 Co. Cork: W6658 (NT2), Glinny, Riverstick; 9-29 August, 2005, 2 males and 1 female; males from Malaise trap in seasonally-flooded, mesotrophic freshwater marsh with patches of bare ground and clumps of Carex riparius; female from Malaise trap in seasonally-flooded, unimproved, disused, Deschampsia/Molinia grassland, coll, and det. M.C.D. Speight; specimens deposited in collections of National Museum of Ireland. Tetanocera montana was first described, from North America and later recorded from Europe. It is one of only three European Tetanocera species in which there is normally a distinct bristle on the postero-dorsal surface of the hind femur, in addition to the bristles on its antero-dorsal surface. Of these three species, the northern European T ornatifrons (not known south of Finland) has black marks on the frons and beside the antennae, these marks being absent in the other two. These other two species, T arrogans and T montana, are more difficult to distinguish. However, T. montana has a dark brown mark, medially, on the occiput (see Fig. lb), that is absent in T. arrogans and the anterior of the two fronto-orbital bristles is also positioned differently in these two species (see Fig. 1), being closer to the anterior margin of the frons in T montana than in T arrogans. Essentially, in T arrogans (Fig. la) the anterior fronto-orbital is closer to the corresponding hind ocellus than to the anterior margin of the frons, whereas in T. montana (Fig. lb) this bristle is about equidistant from hind ocellus and anterior margin of the frons (although there is some variation in the position of these bristles in T. montana). Further, the surstyli of the male DIPTERA NEW TO IRELAND 89 terminalia are very different in appearance in these two species, when examined in external view. In T. arrogans the surstyli are heavily sclerotised, and each surstylus ends in two blunt, dark brown/black points, whereas in T. montana the surstyli are distally thin and transparent, each surstylus ending as an evenly rounded lobe. These differences are well shown in the figures provided by Rozkosny and Jeremies (1977) and Vala (1989), although the figure of T. arrogans surstyli is more accurate in the former and that of T. montana is more accurate in the latter. By contrast, the figures in Knutson and Lyneborg (1965) show the surstyli of these species in lateral view, from which direction they appear almost identical. Features of the male terminalia remain the most reliable means of identifying not only Tmontana, but also other Tetanocera species. Figure 1. Head viewed from above, a = Tetanocera arrogans', h = T. montana. Solid black circles denote insertion points of fronto-orbital bristles; solid patch of stippling indicates position of dark brown mark on occiput of T montana. The antennae and insertion points of other bristles are omitted from the figures. Existing keys to the separation of European Tetanocera rely heavily on the presence of the postero-dorsal bristle on the hind femora as a mechanism for separation of T. montana (and T. arrogans) from other species. However, this bristle is not infrequently absent from one or the other hind femur, making it necessary to check both femora. Eurther, it is apparent that this bristle may be lacking (or, at least, so small as to be indistinguishable from the general hair covering of the femur) from both hind femora in some specimens. A female specimen of T. montana in which the posterO“dorsal bristle is lacking from both hind femora would key out as the common species T. ferruginea in existing keys. About the only feature that might be used to distinguish such specimens of T. montana from T. ferruginea would be the dark brown mark found on the occiput of T. montana, which is absent from T. ferruginea. The reliability of records of T. montana based on solitary females would be open to question, in the absence of additional features for separation of this species. Males of T. montana can be easily distinguished from T. ferruginea by the very different appearance of their surstyli, which should be checked in any case of doubt. Both T. arrogans and T. ferruginea were recorded frequently in Malaise traps catches from the farm in Co. Cork, and both of them were also taken in emergence traps there (Speight, 2004), Further, both of these species were found on the farm in the same Malaise trap samples as T. montana, showing that all three species can occur as adults in the same place at the same time of year. 90 ENTOMOLOGIST’S RECORD, VOL. 119 25.iii.2007 In western Europe T. montana is known from Lapland south to Belgium, and has not been found in Britain. It is only recorded from the Czech Republic and Hungary in central Europe. Further East it occurs in Siberia and Mongolia, and further south in Portugal, the Ukraine, Armenia and Turkey. This is a strangely patchy distribution. The species isn’t particularly difficult to identify so its distribution in Europe presumably reflects other factors in operation. In general, Tetanocera species are easy to collect using either Malaise trap or sweep net. The freshwater marsh, with patchy, tall vegetation and small areas of bare ground, where two of the specimens from the farm were found, closely resembles the only other locality from which the author has collected this species, on the shores of the Baltic, in Finland. In both instances the ground surface remains humid and damp, if not flooded, throughout the year, including during the summer months. Equally, at times of inundation the ground surface of these sites is only shallowly flooded. If T. montana requires such conditions habitat availability might be expected to limit its occurrence under the climatic regime of Europe’s continental zone, a situation that could only be exacerbated by the widespread drainage of wetland that has affected all EU countries latterly, during processes of agricultural improvement etc. Whether T. montana should be regarded as a threatened species in Ireland is moot - certainly the other Tetanocera species known from Ireland have all been recorded repeatedly. Further, the author has specifically sought T. montana in Ireland over the past 30 years, with the thought that there seemed no good reason for its apparent absence. In that context it is perhaps of note that the species has now been found in Ireland in a small area of marsh (“created overland-flow wetland” - see Speight and Good, 2005) constructed on the farm in the autumn of 2002, specifically for biodiversity maintenance purposes, rather than in some long-established wetland of recognised international scientific interest! A parallel Malaise trap survey of the farm, that sampled all habitats accessible to Malaise trapping, and which was conducted during 2000, produced no material of T. montana. But presumably T. montana was “lurking” somewhere in the vicinity of the farm for it to be able to colonise the wetland introduced to the farm once that wetland was available. As described elsewhere (Speight and Good, 2001; 2005), the farm is situated within a rather homogenous, farmed landscape. There are no wetlands of any significant size in its vicinity. Neither the larva nor the puparium appear to have been described for T. montana, although biological information on its developmental stages (in North America) is given by Foote (1999). He found the aquatic larva in the wild, on decaying leaves and stems of a sedge floating in the standing water of a swamp. Once transferred to the laboratory these larvae predated Gyraulus, Lymnaea, Planorbis and Physella species. In continental Europe, adults of T montana are known to occur from June to September. Tetanocera montana remains an enigmatic species. The available information certainly gives no indication as to why it might turn up in a small, recently- established marsh on a farm, rather in better-known wetlands of recognised scientific interest. And is the species really absent from Britain? That seems most unlikely. DIPTERA NEW TO IRELAND 91 References Chandler, P., (ed.), 1998. Checklist of insects of the British Isles (New Series), Pt.l, Diptera, 234pp. Royal Entomological Society, London. Cole, J., 1997. Further British records of Pherbellia rozkosnyi Verbeke (Diptera, Sciomyzidae). Dipterists Digest (Second Series), 3:61. Drake, C.M., 1993. A review of the British Opomyzidae. British Journal of Entomology and Natural History C. 159-176. Fonseca, E.C.M. d’Assis, 1978. Dolichopodidae (Diptera, Orthorrhapha, Brachycera). Handbooks for the identification of British Insects, IX, Pt.5: 1-90. Foote B.A., 1999. Biology and immature stages of snail-killing flies belonging to the genus Tetanocera (Diptera: Sciomyzidae). III. Life histories of the predators of aquatic snails. Annals of Carnegie Museum, 68: 151-174. Good, J.A., 2001. Farms as biogeographical units: 1. Habitat and faunal changes as influenced by farmer decision-making on a mixed farm in south Cork, Ireland. Bull. Ir biogeog. Soc., 25: 220-247. Helden, A.J. & Sheridan, H, 2006. An Irish population of the little-known planthopper Paraliburnia clypealis (Horn., Delphacidae) in a very unexpected habitat. Ir.Nat.J., 28: 232-239. Knutson, L.V. & Lyneborg, L., 1965. Danish Acalypterate flies, 3. Sciomyzidae (Diptera). Entomologiske Meddelelser, 34: 61-101. Negrobov, O.P. 1979. Dolichopodidae. In Lindner, E. (ed.), Die Fliegen der palaerktischen Region, 4 (5), Lief. 32: 475-530. Parent, O., 1938. Dipteres Dolichopodidae. Faune de France, 35: 720pp. Lechevalier, Paris. Pollet, M., 2000. Een gedocumenteerde Rode Lijst van de slankpootvliegen van Vlaanderen. Mededelingen van het Instituut voor Natuurbehoud 8. Brussels, 190pp. Perry, I., 1990. Two species of Pherbellia (Dipt: Sciomizidae) new to Britain. Dipterists Digest 6: 41. Rozkosny, R., 1991. A key to the Palaearctic species of Pherbellia Robineau-Desvoidy, with descriptions of three new species (Diptera, Sciomyzidae). Acta Entomol. Bohemoslov., 88: 391- 406. Rozkosny, R. & Jeremies, M., 1977. Bestimmungstabelle der mitteleuropaischen Sciomyzidae (Diptera). Entomologische Nachrichten, Dresden. 21: 30-64. Ryder, C., McDonnell, R.J. & Gormally, M.J., 2003. Colobaea distincta (Meigen): a sciomyzid (Diptera) new to Ireland with a key to the Irish species of the genus. Ir. Nat. J., 27: 184-186. Speight, M.C.D., 2004. Predicting impacts of changes in farm management on sciomyzids (Diptera, Sciomyzidae): a biodiversity case study from southern Ireland. Dipterists Digest, 11: 147-166. Speight, M.C.D. & Good, J.A., 2001. Farms as biogeographical units: 4. Concept and reality. Bull. Ir. Biogeog. Soc., 25: 292-300. - , 2005. Farms as biogeographical units 5: the response of Odonata to increased habitat availability on a farm in Co. Cork, Ireland. Bull. Ir. biogeog. Soc., 29: 262-277. Vala, J.-C., 1989. Dipteres Sciomyzidae Euro-Mediterraneens. Faune de France, 72, 298 pp. Federation Frangaise des Societes de Sciences Naturelles, Paris. 92 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 Craniophora ligustri D,&S, (Lep.: Noctuidae): from rarity to population explosion at Dartford, Kent and melanism Scattered, references for north-west Kent during the 19th century are listed by Chalmers-Hunt (1965. The Butterflies and Moths of Kent, SuppL Ent. Rec.ll: 265) to be followed by an absence of records for the 20th century, and the comment that the species is probably extinct in this region, including the well-worked Darenth Wood. However, I encountered a specimen at my garden mv light on 3.vii.l969, where numerous ash Fraxinus excelsior trees and saplings grew close by. The next C. ligustri did not arrive until 18.vii.l984, followed by others 28. vi. 1986, 10.viii.l995 (2), 20.vii.l996 and 9.vii.l998. Thus after a long absence of any reference to the species it could nave been regarded as a rarity during the last thirty years of the 20th century. From 2001, it has been seen every year — 2001 (3), 2002 (1), 2003 (4) and 2005 (10). In 2006, a remarkable total of 98 was observed, with contributions of 11 on 6 July and 10 on 11 July, it thus being the commonest of the Acronictinae , far outnumbering Cryphia algae (Fabr.) - 75, Acronicta rumicis (L.) - 49, A. psi (L.) - 36 C. perla (D.&S.) - 32 which, excepting C. algae, have declined in numbers, as have the other resident species not mentioned. There has been some confusion regarding nomenclature relating to the aberrant forms of this moth. Melanies are usually reported as being ab. coronula Haw., as for example by Skinner (1984. Moths of the British Isles, plate 5, fig. 12), a form described by Kettlewell (1973. The Evolution of Melanism: 554) as a geographic (northern), now industrial melanic. However, Haworth’s description includes no reference to the dark greenish- sheen usually seen on melanic C. ligustri in south-east England in recent years, such as in north-west Kent and Chippenham Fen, Cambridgeshire. Tutt (1891. British Noctuae and their Varieties. Ill: 13), lists three melanic forms of C . ligustri and describes each briefly, as follows: 1. ab. coronula Haw. (1809) fuscous (alls fuscis). Tutt states that he had frequently captured it at Strood, Cuxton and other places in mid-Kent and had received specimens from South Wales. 2. ab. olivacea Tutt (1888) suffused with dark olive green. An extreme form in which the green with which the type is suffused in the darker parts of the anterior wings extends over the whole of them. It was reported from south Yorkshire. 3. ab. nigra Tutt (1890) the anterior wings, head, thorax and body intense black, and no trace of green. Tutt knew it only from Doncaster and considered it rare. The descriptions of these three melanic forms are quite different, and Tutt when considering ab. coronula stated that he had collected it frequently from Strood, Cuxton and. other places in Kent, yet he described ab. olivacea from specimens from Yorkshire. Evidently his Kent captures were different from the dark, greenish Yorkshire moths, displaying neither greenish colouring nor greenish sheen. Today, at Dartford almost all melanics of C. ligustri are very distinctly greenish; however, this colour and the curious sheen: of similar- tint are fugitive and are not to be observed on older cabinet specimens. Thus it appears that these 19th century melanics in north NOTES 93 Kent were different from those of to-day. Tutt’s evidence for those early melanics not being ab. olivacea seem sound, while those of to-day fit accurately Tutt’s description of this form. Accepting that these three melanic forms are distinct as seems evident from Tutt’s experience and action, I conclude that the melanics I have encountered at Dartford, with two exceptions, are best regarded as ab. olivacea , but of non-industrial type in view of their persistent very high incidence, close to 100%, during a period of general decline in industrial melanism. A majority of these specimens retain white markings on the thorax to a varying degree . My garden mv light has attracted two extreme melanics, on 28, vi. 2001 and 2.vii.2006, with intensely black forewings, head, thorax and body, and with no trace of greenish tint, identified as ab. nigra and is apparently rare and not previously noted for Kent. If the ab. olivacea which form the vast bulk of the melanics in north- west Kent are non-industrial as suggested, it is surprising that elsewhere in the county the form has not been reported, although Chalmers-Hunt {op. cit.) mentions the capture of an ab. coronula at Ham Street, but could it have been identified as ab, olivaceal This exemplifies the confusion over the nomenclature of the melanic forms of C. ligustri emanating largely from the arbitrary manner in which the textbooks have included, or excluded them, subsequent to Tutt’s work in 1891. For much of the 20th century, South (1909 & 1937. The Moths of the British Isles) was the most popular and an informative work; this, and Newman & Leeds (1913. Text Book of British Butterflies and Moths) both mention only ab. olivacea and ab. nigra. Not until Heath et al. (1983. The Moths and Butterflies of Great Britain and Ireland) list all three forms, with brief descriptions and an unidentified illustration, add ab. coronula again, Skinner {op. cit.) lists only one melanic coronula, and a photographic illustration labelled thus. Of considerable significance, however, is the unpublished work of Goodson and Reid for internal use at the British Museum (Natural History) and used particularly respecting the national (RCK) Collection. In it, beneath the description of ab. olivacea, is the sentence “Probably the same as Haworth’s coronula’) I find Tutt’s experience contradicts this. The problem commenced in the 1890s with the publication of Tutt’s work, before then there were no possible synonyms. Thus, Barrett (1896. The Lepidoptera of the British Islands, III: 272) was aware of variation in C. ligustri noting that the ground colour of the forewings might be deeper olive-green, or deep olive-brown or even almost purplish-black; white markings obliterated, dark markings intensified and hindwings darker. He wrote simply that “these dark forms are some times called collectively by the name ab. coronula, a name which Haworth appears to have used to designate agrey variety which he looked on as a distinct species”. However, this was already outdated by Tutt’s naming and describing ab. nigra and ab. olivacea and the new textbooks of the 20th century ignored mention of Haworth’s variety. Subsequently two authorities have suggested that the three forms are synonymous, despite Tutt’s clear evidence that they are distinct and to-day’s most popular textbook features only Haworth’s somewhat doubtful appellation. The practical 94 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 outcome of this is one is that not sure if the melanic C. ligustri of north-west Kent named as ab. olivacea are the same as those in Surrey which Collins (1997. Larger Moths of Surrey) labelled ab. coronula. Also, what of Chalmers-Hunt ‘s melanic from Ham Street identified as ab. coronula Was it not a deep greenish colour like the contemporary specimens from north-west Kent? The solution - if the dark greenish melanics are labelled ab. olivacea and the extreme black ones ab. nigra, both easily identified, any others perhaps ab. coronulal — B. K. West, 36 Briar Road, Dartford, Kent DA5 2HN. Tomoxia bucephala Costa (Col.: Mordellldae): A case of long persistence in the same locality I was interested in Mr R. A. Jones’ record of two examples of Tomoxia bucephala ‘crawling on [a] large fallen beech log in Arundel Park, West Sussex, 18.vi.l976’. I would guess that this log was, in fact, the very same one on which I first met with this beetle as long ago as 1935 and on one or two later occasions. The identical log was still in situ many years later when it yielded, notably, the very rare Laemophloeus monilis Fabr.). The log was situated under one of the fine beech trees for which the park is notable and the beetles ran and flew so actively in the hot sunshine as to be hard to catch. Elsewhere, I have encountered the species only in a rather out-of-the-way part of Windsor Forest, also about beech stumps, on one occasion. — A. A. Allen, 49 Montcalm Road, Charlton, London SE7 8QG. SUBSCRffiER NOTICE I have just started my PhD project on macroecology of European invertebrates. As a part of the project I am putting together a database of published papers about Syrphidae from ail Europe. In particular, I am interested in published local faunal lists, inventory studies, checklists and also unpublished material (MSc, PhD theses). I would like to ask you if you could provide me with reprints of photocopies of your publications which match these criteria. I would appreciate receiving copies of older studies, published by other authors, which you would consider as rare or hard to obtain. In case of any questions do not hesitate to contact me. — Petr Keil, Department of Ecology, Faculty of Science, Charles University in Prague, Vinicna 7, 12800 Praha 2, Czech Republic (E-mail: pkeil@seznam.cz). BOOK REVIEWS 95 BOOK REVIEWS Pyraloidea of Europe/Europas (Lepidoptera) Volume/Band 1: Pyralinae, Gelleriinae, Epipaschiinae, Cathariinae and Odontiinae by F* Slamka. 144pp., including 16 colour plates of adult moths and 11 black and white plates of genitalia. 232 X 165 mm, hardbound. ISBN: 80"969052-3-6.Published by Slamka, Bratislava, December 2006. €49 (plus postage). Bilingual: English and German. Order direct from Slamka, RaEianska 61, SK-83102 Bratislava, Slovakia or by e-mail to slamkaf@nextra.sk (web site at http://home.nextra.sk/fslamka). This book is from the same publishing stable as Josef Rasowski’s Tortricidae of Europe - a fact that is immediately apparent from the near identical covers. Slamka have also produced, in recent years, Die Zunslerartigen (Pyraloidea) Mitteleuropas (Slamka, 1997), The Noctuids of central Europe (Nowacki, 1998), Die Palpenmotten (Geiechiidae) Mitteleuropas (Eisner et al, 1999) and Die Oecophoridae Mitteleuropas (Tokar et al, 2005) - four books that deserve places in the personal library of any serious British lepidopterist. The man at the helm, Dr Frantisek Slamka, has specialist knowledge the Pyraloidea; consequently, this first volume of Pyraloidea of Europe has been very much a labour of love. The British Isles are included in the geographical area covered by the work, which incorporates all of Europe from Iceland in the north-west, east to the Ural Mountains, south- east to the Caucasus Mountains and south to the Straits of Gibraltar. All of the Mediterranean Islands are involved - including Cyprus, an island that is, unfortunately, omitted from most European works. European Turkey is included, but Asian Turkey is not. Species from the Azores, Canaries and Madeira are also listed. A total of 117 species is included in the work and distribution maps are included for each. Adult moths are illustrated at 1 .5 times natural size by means of colour photographs and space saving has been achieved by showing only the right hand half of each species. Genitalia are illustrated by black and white photographs for both sexes of 41 ‘problem’ species. All species are allocated a serial number, so that text, genitalia and colour plate have the same number for each taxon, making the book very easy to use. Dipping into the text in random fashion I observe that for many difficult to separate species text figures are also provided and furnished with short lines, pointing to the character that permits satisfactory identification. I have not really had the book long enough to find all the errors and there are bound to be a few in a work of this nature, but having met with Slamka and having reviewed his “track record” I expect that there will be rather few! This is the first in a projected series of what are, essentially, identification guides covering the entire of the European Pyraloidea. This first volume contains rather few British species and some may judge it to be of limited use to English-only collectors - but then when the other 96 ENTOMOLOGIST'S RECORD, VOL. 119 25.iii.2007 more useful volumes appear you will regret not having the complete series! If you collect in Europe it will be essential. Of course, there are other promised works on the Pyraloidea from other sources. The series Microlepidoptera of Europe is well worth the cost, but only one volume concerning pyraloids is yet published. Those who live long enough may yet see the pyralid volume of Moths and Butterflies of Great Britain and Ireland in print. My personal view is that one can never have too many books; how many times have I failed to find information in one tome then found it in another! At €49 (about £33) I recommend that you buy this volume now, before it goes out of print! Ecology, Phenotypes and the Mendelian Genetics of Burnet Moths {Zygaena Fabricius, 1775) by W. Gerald Tremewan. 390 pp., 194 figures (163 in colour), 235 X 156mm., hardback. ISBN 0 906802 1 1 3. Gem Publishing Co, 2006. £79. This is a work of enormous scholarship, detailing the results of Gerry Tremewan’s genetic studies on burnet moths since he began these studies in 1977. He has managed the technically very difficult task of breeding these moths, so as to elucidate the mendelian genetics of many of the beautiful and striking variant forms that occur, including specimens with yellow instead of red markings, or with confluent rather than discrete spots, or those with extra spots. To successfully complete so many broods is almost unimaginably difficult, especially in the context of producing sufficiently large numbers of specimens in 1st and then 2nd back- crossed generations, to allow determination of the ratios of forms and therefore the dominance or other expression of the forms under investigation. No wonder that the body of work was successfully presented for a doctorate in 2002. This is not all. The early part of the book includes an extended and authoritative account of the general biology of burnet moths, which successfully sets the scene for the genetic study. This section alone is of great interest but the meat of the book is a series of explanations of the genetics of the many variant forms, culminating with a chapter on hybridisation. The text is very full and necessarily detailed but of a standard format, so that the reader can easily get used to what is being explained. Tables and diagrams illustrate the mendelian ratios that were found and finally there are many excellent colour illustrations (often taken by the author) that amply illustrate the forms under discussion. Overall this is a beautifully produced and presented book, that will interest anyone interested in the genetics of insects, and/or the biology of burnet moths. The drawback is the price but I suppose this is inevitable for a book with so many colour illustrations and with a limited audience. However, in the context of the authority and scope of the work reported, it is not really too expensive and any reader will find continuing pleasure in its study. ■ {Zygaena Fabricius, 1775) Mark Young Continued from back cover A naturalised population of a Mediterranean earwig, Forficula pubescens Gene (Derm.: Forficulidae) in West Sussex. John Paul 83-84 Craniophora ligustri D.&S. (Lep.: Noctuidae): from rarity to population explosion at Dartford, Kent and melanism. B. K. West 92-94 Tomoxia bucephala Costa (Col.: Mordellidae): A case of long persistence in the same locality. A. A. Allen 94 Subscriber Notice European invertebrates. Petr Keil 94 Book Review Pyraloidea of Europe/Europas (Lepidoptera) Volume/Band 1: Pyralinae, Gelleriinae, Epipaschiinae, Cathariinae and Odontiinae by F. Slamka 95-96 Ecology, Phenotypes and the Mendelian Genetics of Burnet Moths (Zygaena Fabricius, 1775) by W. Gerald Tremewan 96 Experience the lighter side of field entomology with Torben Larsen as he describes his experiences from around the world. There must be a Hazard for every occasion? £11.99 (inc. UK p&p) * £1 3.99 (overseas) ORDBt YOUR COPY NOW FROM Cravitz Printing Company Limited 1 Tower Hill, Brentwood, Essex CM14 4TA. Tel: (01277) 224610 • Fax: (01277) 262815 • E-mail: CravitzPrinting@btconnect.com THE ENTOMOLOGIST’S RECORD AND JOURNAL OF VARIATION http://www.entrecord.com Papers Butterflies on farmland: The first 10 years of recording at Writtle College. R. G Field and T. Gardiner 49-56 Uresiphita reversalis (Guenee, 1854) (Lep.: Pyralidae) new to Britain and Europe. Tony Davis and Doug Miller 59-61 Nineta pallida (Schneider, 1846) (Neu.: Chrysopidae), a lacewing new to the British Isles. Martin C. Harvey and Colin W. Plant 77-82 Rhaphium nasutum (Diptera: Dolichopodidae), Pherhellia rozkosnyi & Tetanocera Montana (Dip.: Sciomyzidae), insects new to Ireland and Geomyza halachowski (Dip.: Opomyzidae), presence in Ireland confirmed. Martin C. D. Speight 85-91 Notes Cornifrons ulceratalis (Lederer, 1858) (Lep.: Crambidae) new to France and Syncopacma albifrontella (Heinemann, 1870) (Lep.: Gelechiidae): first published French record. Michael & Brenda Marney 56-58 Nest building and prey stocking in Crossocerus megacephalus (Rossius) (Hym.: Sphecidae). P/pcr 58 The advantages of ‘Doing the Dirt’: New and interesting moth records for Hertfordshire & Middlesex. Rachel Terry 62-63 Late-flying Silver-ground Carpets Xanthorhoe montanata D. & S. (Lep.: Geometridae) in Banffshire. /?6>yLevmo« 63 Notes on the early stages of Elachista regificella Sircom, 1849 and E. tengstromi Kaila et al, 2001. John R. Langmaid 64-65 Hazards of butterfy collecting. Bumbuna Butterfly Survey - Siena Leone, May 2006. Torhen B. Larsen 65-67 Lepidoptera new to the Isle of Wight in 2006. Sam Knill-Jones 67-68 I married a Moth Man - a warning to new moth spouses. Pat Costen 68-7 1 Scythris potentillella (Zeller) (Lep.: Scythrididae) new to Hertfordshire. David Murray 71 Pale Shining Brown Polia bomhycina (Hufn.) (Lep.: Noctuidae) re-discovered in Oxfordshire in 2005 and 2006 - a nationally significant population of a UK Biodiversity Action Plan Priority Species. Martin C. Townsend and Thomas Merckx 12-1 A Diaperis boleti (L.) (Col.: Tenebrionidae) in Hatfield Forest, Essex. Ross Piper 74-75 Red Admiral Vanessa atalanta (L.) (Lep.: Nmyphalidae) courtship in winter. Richard Fox 75-76 Atlantopsocus adustus (Hagen) (Psoc.: Psocidae) new to Britain from East Cornwall. Keith N. A. Alexander 76 An invasion of the Harlequin Ladydird (Harmonia axyridis Pallas) (Col. Coccinellidae) in the South Wight. Sam Knill-Jones 82 SMITHSONIAN INSTITUTION LIBRARIES 3 9088 01327 0491 Printed in England by Cravitz Printing Company Limited, 1 Tower Hill, Brentwood, Essex CM14 4TA. Tel: 01277 224610 PUBLISHED BI-MONTHLY Entomologist’s Record Journal of Variation H S ant, b.sc., F.R.E.S. May/June 2007 ISSN 0013-8916 THE ENTOMOLOGIST’S RECORD AND JOURNAL OF VARIATION World List abbreviation: Entomologist’s Rec. J. Var. http://www.entrecord.com Editor C.W. PLANT, B.Sc., F.R.E.S. 14 West Road, Bishops Stortford, Hertfordshire CM23 3QP. Telephone/Facsimile: 01279 507697 E-mail: cpaukl@ntlworld.com Registrar Treasurer R.F. McCormick, f.r.e.s. C.C. Penney, f.r.e.s. 36 Paradise Road, 109 Waveney Drive, Springfield, Teignmouth, Devon TQM SNR Chelmsford, Essex CMl 7QA WHERE TO WRITE EDITOR: All material for publication, including books for review and advertisements REGISTRAR: Changes of address TREASURER: Subscriptions and non-arrival of the Journal Readers are respectfully advised that the publication of material in this journal does not imply that the views and opinions expressed therein are shared by the Editor, the Entomologist’s Record Committee or any party other than the named author or authors. Entomologist’s Record and Journal of Variation is a non profit-making journal, funded by subscription, containing peer-reviewed papers and shorter communications. It is published by the Entomologist’s Record Committee, comprising the Editor, the Registrar and the Treasurer, from the Editorial address. An Editorial Advisory Panel exists to assist the Editor in his work. The annual subscription for year 2007 is £28 for individual subscribers or £50 for institutions. INSTRUCTIONS TO CONTRIBUTORS • This journal publishes peer-reviewed papers and shorter Notes that are reviewed by the Editor. Contributions are accepted on merit, with no regard whatsoever to the occupation or standing of the author. All contributions should bear the name and postal address of the author(s), but titles or honours are not permitted and will be removed. One e-mail address may also accompany the contribution. First time authors and non-subscribers are welcome to send material for publication. We are able to include colour photographs from time to time at no cost to the author(s). Good quality monochrome photographs are always welcomed. • The journal is concerned with British Lepidoptera (moths and butterflies). We also accept contributions on British Coleoptera (beetles), British Diptera (flies) and other groups at the Editor’s discretion. We also print Subscriber Notices at no cost on behalf of current subscribers; non-subscribers pay a fee for this service. We also publish Reviews of entomological books and other publications relating to all aspects of world entomology if these are sent to the Editor at no cost to him. It is our policy not to accept unsolicited book reviews from third parties. • We may also accept contributions on European insects if these are likely to be of interest to British readers, such as species likely to colonise Britain (especially where these contributions include identification keys or photographs), or accounts of entomological trips to places that may be of interest to other readers. • Papers should be at least 2000 words in length. Acceptance is not automatic. They will be peer-reviewed by two referees. Authors must be prepared to make modifications suggested by the referees. Papers must cover their subject matter to a far greater depth than Notes and should present original material or a broad-based review of existing knowledge. Descriptions of new species may be submitted. Authors of papers are expected to follow the house style and conventions as closely as possible. The Editor reserves the right to convert papers into Notes. • Notes are the meat of the journal! Most contributions will fall into this category. They will normally be less than 1 500 words in length and can be very short indeed as long as the information they impart is interesting. We welcome Notes. There is no limit to how many you can contribute. Authors of Notes should try as far as possible to follow the house style and conventions, but the Editor will attend to these if errors are made. • We accept all formats from hand-written notes upwards. However, we prefer submissions via e-mail, or on CD. Files must be in a PC-compatible format that is readable by Microsoft Word. Originals are required for all photographs, drawings, diagrams, graphs, histograms and similar, though Tables may be incorporated into word processor files. For details, visit the web site or contact the Editor direct. WATER BETONY IN CHANNEL ISLANDS 97 WATER BETONY SHARGACUCULLIA SCROPHULARIAE (D. & S.) (LERt NOCTUIDAE) NEW TO THE CHANNEL ISLANDS Philip H. Sterling' and Peter D. M. Costen^ ^Environmental Services, Dorset County Council, County Hall, Colliton Park, Dorchester, Dorset DTI IXJ. ^La Broderie, La Claire Mare, St Peters, Guernsey GY7 9QA. Abstract The discovery of Water Betony Shargacucullia scrophulariae (D. & S.) (Lep.: Noctuidae) new to the Channel Islands (VC 113) is reported. Introduction On 8 June 2005, PDMC found in his garden trap a moth which initially he thought was a small specimen of Mullein Shargacucullia verbasci (L.) Although in poor condition, it was retained in preparation for a visit to Guernsey later that year by PHS. In anticipation of his customary advice when invited to identify specimens in this state, the specimen was dissected, whereupon it was immediately apparent that this was not a Mullein. It was a male and the shape of the valves was distinctively different from that of Mullein, and the conclusion was reached that it was a specimen of Striped Lychnis Shargacucullia lychnitis Rambur, This is a species which has been recorded from Guernsey on at least two previous occasions (Shayer, 1975; Higgs, pers. comm.) and was of interest given the virtual absence from the island of its usual foodplant Dark Mullein Verbascum nigrum. However, when the specimen and slide were seen by PHS, he was less than convinced of this identification as neither the time of year of appearance, nor the shape of the valves of this example, was consistent with that species. Then, on each of the nights of 3 June 2006 and 10 June 2006 PDMC found another similar specimen in his trap. These were again set and on this occasion PHS was able to travel to Guernsey to dissect both moths himself. On dissection the appearance of the genitalia was strongly suggestive of Water Betony Shargacucullia scrophulariae ([D. & S.]), based on the description and figures in Ronkay & Ronkay (1994). On returning home, PHS dissected an example of Striped Lychnis reared from a larva, and the differences between genitalia of this and the Guernsey examples were immediately obvious: undoubtedly all three of the Guernsey examples were Water Betony. Comparison with similar species Adults of Mullein, Striped Lychnis and Water Betony are similar, especially when worn. Although Mullein is larger and generally darker brown with a more scalloped termen in the forewing, worn examples flying in May or June can be paler with scalloping much reduced, making them look smaller and similar to Water Betony which flies at the same time. Striped Lychnis is much the latest of the three on the wing, sometimes in late June, but mainly in July, hence PHS's interest in the putative 98 ENTOMOLOGISTS RECORD, VOL. 119 25.V.2007 identification of this species from early June. It appears that the only way to be sure of identity of a worn example is via dissection. The genitalia of both sexes of all three species are figured in Ronkay & Ronkay {op. cit.). A simplified guide to identification of the male is given below, based on examination of our material only. The literature suggests more variation than we observed, particularly in the number and size of teeth on the ventrum of the aedeagus, so some caution may need to applied to this character. We consider there may be reliable shape and size of teeth within the carina of the aedeagus which help distinguish the species without need to evert the vesica, although with eversion, the origin of the distal part of the main tube of the vesica allows distinction to be made between Striped Lychnis and Water Betony. The valves of Striped Lychnis and Water Betony show subtle diagnostic features, but are obviously different from those of Mullein. Photographs are shown of male genitalia only of Water Betony (Figs 1, 2 & 3), Striped Lychnis (Figs 4, 5 & 6), and Mullein (Figs 7, 8 & 9). Table 1 summarises diagnostic characters of the male genitalia of the three species; Table 1. Diagnostic features of male genitalia of Shargacucullia spp. Water Betony Shargacucullia scrophulariae Striped Lychnis Shargacucullia lychnitis Mullein Shargacucullia verbasci Valvae Valvae long. Harpe broad before apex, with apical corona well developed; width of corona about 3x minimum width of harpe Valvae Valvae very long. Harpe broad before apex, with apical corona well developed; width of corona more than 3x minimum width of harpe Valvae Valvae short. Harpe narrows to apex which may be produced into a digit; apical corona short, reduced to 4 - 6 bristles Aedeagus Carina of strong teeth, more or less arranged in a single row nearly reaching ventrum, with smaller teeth on dorsal side of row; ventral projection a small pair of teeth; distal part of main tube of vesica arises dorsally, not dorso-laterally. Aedeagus Carina of strong teeth in an elongate patch, more or less parallel sided, nearly reaching ventrum; ventral projection a pair of large teeth; distal part of main tube of vesica arises dorso-laterally, not dorsally. Aedeagus Carina of strong teeth along dorsum and in subtriangular patch reaching just beyond half way to ventrum; ventral projection a single large tooth. For the sake of completeness the genitalia of the females of the three species are included, reproduced from the figures in Ronkay & Ronkay {loc. cit.) (Fig. 10). The species can be separated by the shape of the corpus bursae and the shape and sclerotization of the ostium bursae. Comments on records and distribution Water Betony has long been considered to be a British insect. Tutt (1891) writing in this journal 115 years ago believed it to be undoubtedly British and 75 years later Chalmers-Hunt (1966) described it as resident, perhaps native. These authors were WATER BETONY IN CHANNEL ISLANDS 99 referring to Victorian records from East Anglia and Kent respectively but in more recent years the only two substantiated records have both been from Swanage in Dorset. On 12 June 1949, at 3.30 a.m., A.G.B. Russell took a specimen at light (Russell 1950), the identity of which was confirmed by Boursin whom Russell described as the foremost authority on the Cucullia group, and on 18 May 1994, at MV light, J.H. Clarke took another specimen (Davey 1996), the identity of which was confirmed by dissection at the British Museum (Natural History). The moth has not been recorded previously from the British Channel Islands but was noted on the French Channel Island of Chausey in June 1995 (Livomy pers. comm.). And in La Manche region of Normandy, that part of the French mainland closest to Guernsey, in contrast to Striped Lychnis which has been recorded on just two occasions (and then from the south of the region). Water Betony has been recorded from all parts and is described as peu commun; jamais en nombre mais regulier albeit with the caveat that Mullein, Striped Lychnis and Water Betony are difficult to distinguish from each other than by the characteristics of their larvae. Larvae of Water Betony feed on the flowers and seeds of Scrophularia species, mostly S. nodosa Common Figwort (Ronkay & Ronkay loc. cit.), but this is by no means a common plant on Guernsey (Ozanne 2006). Water Figwort S. auriculata is frequent here in wet places but by far the commonest member of the group locally is Balm-leaved Figwort S. scorodonia and although many plants have been searched in recent years in the hope of finding larvae of the gelechiid Nothris congressariella (Bruand), no larva of any description has ever been noted. However, it remains a distinct possibility that the Water Betony is resident in Guernsey; the larvae feed up quickly and are only visible amongst the flowers of the foodplant when very small, hiding low down amongst vegetation when bigger (Fibiger pers. comm.). The larvae are, therefore, much less apparent than either those of Mullein or Striped Lychnis on Verbascum spp. Of the two Guernsey examples of Striped Lychnis, the first was captured in 1971 or 1972 (no more detailed data are available) and reported in a list of 19 species which had been submitted to, and confirmed, by the Entomological controller at the Rothamsted Centre (Shayer loc. cit.). The second was taken on 28 May 1989 at MV light in St. Saviour on the west of the island (Higgs pers. comm.). In light of our findings, and the early date of the 1989 record, we consider it that this is more likely to be of Water Betony and should be critically re-examined. Acknowledgements We are grateful to Michael Fibiger (Sor0, Denmark) for his comments during the drafting of this paper, and for allowing us permission to reproduce the figures of the female genitalia from Ronkay & Ronkay {loc. cit.). We are also grateful to Dave Foot (Weymouth) for donating a specimen of Striped Lychnis. 100 ENTOMOLOGISTS RECORD, VOL. 119 25.V.2007 Fig. 1. Male genitalia (valvae) of Water Betony ShargacuculUa scrophulariae (RD.M. Costen coll., slide number PC309) Fig. 2. Male genitalia (aedeagus) of Water Betony ShargacuculUa scrophulariae (RD.M. Costen coll., slide number PC309) Fig. 4. Male genitalia (valvae) of Striped Lychnis ShargacuculUa lychnitis (P.H. Sterling coll., slide number PS 899) Fig. 7. Male genitalia of Mullein ShargacuculUa verbasct valvae (P.D.M. Costen coll, slide number PS897) Fig. 5. Male genitalia (aedeagus) of Striped Lychnis ShargacuculUa lychnitis (P.H, Sterling coll, slide number PS899) Fig, 8. Male genitalia of Mullein ShargacuculUa verbasct aedeagus (P.D.M. Costen coll., slide number PS897) WATER BETONY IN CHANNEL ISLANDS 101 Fig. 6. Male genitalia (carina) of Striped Lychnis Shargacucullia lychnitis (RH. Sterling coll., slide number PS899) Fig. 8. Male genitalia (carina) of Mullein Shargacucullia verbasci (P.D.M. Costen coll., slide number PS897) Fig. 3. Male genitalia (carina) of Water Betony Shargacucullia scrophulariae (P.D.M. Costen coll., slide number PCS 10) Fig. 10. Female genitalia (from Ronkay & Ronkay, 1994). A. Water Betony Shargacucullia scrophulariae; B. Striped Lychnis Shargacucullia lychnitis; C. Mullein Shargacucullia verbasci 102 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 References Chalmers-Hunt, J.M., 1966. Lepidoptera of Kent page 273 published as supplement to Entomologist’s Rec. J. Van 78 between pages 28-29. Davey, R 1996. 1994 Moth immigrations to Dorset and potential sources of origin. Proc. Dorset nat. Hist, archeol. Soc. 117: 169-170. Higgs, G.H. Unpublished list of Lepidoptera recorded on Guernsey in 1989. Livomy, A. Unpublished list of Macrolepidoptera recorded on Les lies Chausey in June 1995. Ozanne, B.J., 2006. Check List of Guernsey Plants. La Societe Guemesiaise, Guernsey. Quinette, J-R, Lepertel, N., Guerard R. 2004. Inventaire des Macrolepidopteres de La Manche. Rrivately published. Ronkay, G., Ronkay, L. 1994. Cuculliinae 1. - Noctuidae Europaeae, volume 6 -. Entomological Rress, Sor0, Denmark. Russell, A.G.B., 1950. Report on Dorset Lepidoptera, 1949. Proc. Dorset nat. Hist, archeol. Soc. 71: 170-174. Shayer, C.J., 1975. Entomological Report [for 1974]. Report and Transactions of La Societe Guemesiaise. 22(part 4): 368-370. Tutt, J.W., 1891. Cucullia scrophulariae as a British insect. Entomologist’s Rec. J. Van 2:63-64. DEFECTIVE COPIES OF THE LAST ISSUE It has come to my attention that a number of copies of the last issue of this journal were poorly finished. In most cases, this was because the staples were not positioned in the mid line of the paper so that when the pages were folded and cropped the left and right margins finished unequal. In extreme cases text has been cropped and in a few cases blank pages or missing pages were noted. All of these problems are the responsibility of the binders - after the printing stage - and our printers have already taken steps to ensure that this does not happen again. We shall, of course, replace all seriously defective copies at no cost to subscribers. However, we do not have a limitless supply and so we trust to the honesty of our subscribers in this matter. Please petition the Treasurer, not me, if you wish to replace your copy. Those wishing to send a stamped self-addressed envelope are welcome to do so, but this is not a requirement. - EDITOR. DWARF FORM SILVER Y 103 THE DWARF FORM OF SILVER Y AUTOGRAPHA GAMMA (L.) (LEP.: NOCTUIDAE) Roy Leverton Whitewells, Ordiquhill, Cornhill, Banffshire AB45 2HS. Abstract In late August 2006, dwarf individuals of Silver Y Autographa gamma predominated in NE Scotland, but very few were reported from more drought-stricken parts of the British Isles. This conflicts with the generally accepted ‘starvation form’ hypothesis. Instead, a pathological factor is suggested. Introduction The dwarf form of Silver Y Autographa gamma has long attracted attention. It has even acquired its own varietal name, gammina (Staudinger), and is illustrated in guides such as Skinner (1984) and Waring & Townsend (2003). Whereas the ‘normaF moths are quite variable in size, with a wingspan ranging from 40"52mm, gammina is generally between 30-35mm and sometimes less. An exceptional example caught at Peacehaven in Sussex had a wingspan of only 24mm (Colin Pratt, pers. comm.). Also, gammina tends to be light silvery grey in colour, lacking the brown tones often seen in normal-sized moths. Events of 2006 Occasional examples of gammina have been recorded at my home address in Banffshire in previous years, but in 2006 they were exceptionally numerous. For a period during the second half of August, dwarf individuals predominated and even the ‘normal’ moths with them were mainly below average size. Precise counts were difficult because most Silver Ys were seen feeding actively at heather or buddleia by day and at dusk, rather than in the light trap. With such continual movement even estimating total numbers was difficult, let alone the percentage of gammina. Also, there was some intergrade in size between the smaller ‘normal’ moths and the dwarfs, giving a few borderline individuals. Using Bretherton’s (1977) definition of gammina as having a wingspan of 35mm or less, the following table gives rough estimates of its percentage on selected dates. Interpreting these data is difficult. Sometimes the percentage of gammina varied even on the same date, with dwarfs relatively numerous by day and on warm evenings but apparently less active than normal individuals in cooler conditions. Also, the origin of the moths is unknown. Although primary immigrant Silver Ys were unusually numerous here from May onwards, there was no firm evidence that any of the late summer gammina were locally bred. The few caterpillars and cocoons found casually here during the summer were all of normal size. However, other known migrant species were scarce or absent in Banffshire during the main gammina period, giving no suggestion that a mass immigration was in progress. 104 25.V.2007 ENTOMOLOGISTS RECORD, VOL. 119 I also contacted various observers to ask whether they had noticed unusual numbers of gammina in summer 2006. Mark Young at Oldmeldmm in neighbouring North Aberdeenshire confirmed that on some dates up to 50% of Silver Ys were dwarfs in his area. However, Brian Neath saw no dwarfs in Wester Ross, at the same latitude as Banffshire but on the west coast. Further south, Gerry Haggett replied that he had not noticed any gammina in Norfolk that summer, while Colin Pratt provided a figure of 0.2% gammina in Sussex during 2006 from a sample size of 1,384, with none at all seen in August. Such evidence strongly suggests that the gammina in north-east Scotland were locally bred or had not travelled far. Had they been immigrants from abroad they would surely have been at least as numerous further south. Previous explanations for the dwarf form Cockayne (1953) attempted to raise gammina to a subspecies. He reared examples from unusually dark, sometimes almost black, caterpillars he found in Kent. (Normally, wild Silver Y caterpillars are green.) Based on the larval and adult differences, he suggested that it was a genetically distinct immigrant race perhaps originating from the eastern Mediterranean, since Staudinger’s type locality for gammina was Syria. However, he could find no differences in the genitalia, nor did he attempt to breed a further generation of dark caterpillars and dwarf moths. Bretherton (1977) convincingly rejected Cockayne’s hypothesis. He reasoned that subspecies were unlikely to evolve in such a notorious migrant as Silver Y because it lacks genetically isolated populations. Furthermore, he reared progeny from three dwarf females captured in Surrey in August 1976. The caterpillars were the usual shade of green and the adults, though on the small side, were within the normal size range. Accordingly, he argued that gammina is just an environmental 'starvation form’ caused by desiccated larval foodplant in drought years. This has remained the accepted view, despite Cockayne’s explicit rejection of such an explanation {loc. cit.). The undersized black caterpillars he found at Sheemess in Kent were eating the fleshy leaves of orache Atriplex growing on the shore. The foodplant was abundant and very juicy, nor were there any signs of past or present larval overcrowding. He also pointed to several older references in the journals to dwarf black caterpillars of Silver Y, found on various foodplants with no mention of shortage or drought, that went on to produce gammina adults. If the gammina seen in Banffshire during summer 2006 were indeed locally bred, this further undermines the 'starvation form’ hypothesis. Although the weather was exceptionally warm and sunny throughout July, with shade temperatures in my garden exceeding 30°C on several dates, there were no obvious signs of drought. Vegetation remained green and lush. I never needed to water the garden and lawns required frequent mowing. Nor did other species that were in the larval stage at the same time as Silver Y produce dwarf forms - if anything, the resulting moths tended to be larger than average. Drought was far more severe in Norfolk and Sussex, yet the incidence of gammina here was very low. DWARF FORM SILVER Y 105 As a migrant, Silver Y ranges throughout the Holartic from North Africa to beyond the Arctic circle, with breeding proven even in Iceland (Skou, 1991). Clearly it must be able to cope with a wide range of climates and habitats. It can also use a broad variety of foodplants. It seems unlikely that this species would be seriously inconvenienced by a British summer. Admittedly, it would make sense for Silver Y to have the ability to produce an emergency dwarf form when conditions were unfavourable. As a migrant, its caterpillars must often find themselves in a rapidly deteriorating environment. Their best strategy might then be to complete their metamorphosis quickly, even at the expense of producing an undersized adult - which would at least be able to migrate away from the inhospitable area. Attractive though this scenario seems, there is no firm evidence for it. Nor would it explain the very high percentage of gammina in north-east Scotland in 2006 despite the absence of drought, yet its much lower incidence elsewhere. Thus both the ‘subspecies’ and the ‘starvation’ explanations for gammina seem flawed. Tablel. Estimates of the percentage of the dwarf form gammina in counts of Silver Y Autographa gamma in Banffshire on various dates in summer 2006. Date Total % gammina locality & comments 30.07.2006 10 0 Ordiquhill; very fresh - the first locally bred moths? 12.08.2006 100 0 Ordiquhill; on buddleia at dusk. 17.08.2006 360 0 Ordiquhill; m.v. trap catch; many moths on small side. 18.08.2006 300 0 Ordiquhill; on heather by day; many moths smallish. 19.08.2006 100 30 Ordiquhill; on buddleia at dusk. 20.08.2006 150 50+ Ordiquhill; on buddleia at dusk. 25.08.2006 20 60 Ordiquhill; on buddleia by day. 26.08.2006 25 90+ Ordiquhill; on buddleia by day. ” 20 10 Ordiquhill; on buddleia at dusk (cool evening). 30.08.2006 30 80 Macduff (coastal); on flowers by day. ” 25 8 Ordiquhill; on buddleia at dusk (cool evening). 31.08.2006 75 50+ Ordiquhill; on buddleia at dusk (warm evening). 02.09.2006 40 0 Ordiquhill; on buddleia at dusk (cool evening). 10.09.2006 200 0 Cullen (coastal); on heather by day. 14.09.2006 11 9 Ordiquhill; m.v. trap catch. 18.09.2006 45 11 Macduff (coastal); on flowers by day. 22.09.2006 20 0 Ordiquhill; on heather by day; no further gammina sightings. 106 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 An alternative hypothesis I suspect that the gammina form of Silver Y is neither genetic nor environmental, but pathological. Cockayne’s account {loc. cit.) is strongly suggestive of this. He notes that the abnormally small and dark wild-found caterpillars that produced gammina adults were unusually delicate, so that he reared only five moths from the nine larvae he kept. Furthermore, he traced several earlier notes in the journals that made similar remarks. Thus G. T. Porritt bred only one adult from eight undersized dark caterpillars sent to him by Charles Whitehead of Maidstone, who likewise encountered problems: more than half his larvae died without spinning up, while many cocoons of those that did were imperfectly formed and produced no moths. J. C. Miller reared only three gammina from small dark caterpillars found at Beckenham in Kent, the others dying though well fed. Silver Y is normally a very easy species to rear. Majerus (2002) describes the many different pathogens that can affect moths. These include viruses, bacteria, fungi and protozoa. Usually they are most in evidence from the high mortality they can cause when large numbers of caterpillars are being reared in captivity. However, even apparently healthy moths may carry sub-lethal pathogens and transmit them to the next generation through the egg or sperm. If the gammina form is caused by a pathogen, why should this problem disproportionately affect Silver Y? Many other Lepidoptera produce occasional dwarfs, but not on such a scale. Cytoplasmic incompatibility, as defined by Majerus {loc. cit.), is one possibility. Normally this is only seen in the laboratory, when individuals from geographically distant populations are crossed. If these happen to be infected with different strains of Wolbachia bacteria, the crosses may fail or suffer an unusually high mortality rate. For most moths, such crosses will rarely if ever happen in the wild. But Silver Y is an abundant, long-distance migrant, hence mixing of populations infected with different strains of pathogens is a possibility. Maybe gammina is the result of crosses between immigrant Silver Ys of widely separate origins. In most summers, Britain is colonised by streams of Silver Ys coming from the western Mediterranean, which then breed successfully to produce normal moths with few if any dwarfs. Perhaps in certain years some parts of Britain also receive influxes of Silver Y from the eastern Mediterranean, carrying incompatible strains of pathogens (not necessarily Wolbachia). For interbreeding to happen, the two streams would have to arrive almost simultaneously and to overlap geographically, with at least some females receptive to mating. The apparent association of gammina with hot summers could be explained by the weather patterns necessary for such mixing to occur. Alternatively, the condition may be lethal unless the weather is particularly warm and dry. Admittedly, this is only speculation. As a hypothesis, it does at least fit the observed evidence. In late May and June 2006, Britain did indeed receive an unusually strong influx of migrant moths from the south-east, as evidenced by record numbers of Eastern Bordered Straw Heliothis nubigera. It is very likely that some of DWARF FORM SILVER Y 107 our immigrant Silver Ys seen during this period had a similar origin. Perhaps it was mainly in north-east Scotland they overlapped and interbred with incompatible migrants arriving from the south-west. There is one obvious way to take the investigation further. The unusually small and dark caterpillars that produce gammina should hold the key. They could be screened for pathogens at a suitable research laboratory. If any are found, each individual should be immersed in a separate container of ethanol at least 70% strong (preferably stronger) to preserve any pathogen DNA. Acknowledgements I am very grateful to Mark Young and Mark Shaw for their incisive comments on earlier drafts and for much stimulating discussion, though the opinions expressed in this paper remain entirely my own. I thank Brian Neath, Gerry Haggett and Colin Pratt for promptly sending me relevant information from their own areas. Mark Young kindly helped with obtaining references. References Bretherton, R. F, 1977. The status of Auto grapha gamma gammina Staudinger (Lep.: Noctuidae). Proceedings of The British Entomological and Natural History Society 10:27-28. Cockayne, E. A., 1953. A Subspecies of Plusia gamma Linnaeus. Entomologist’s Rec. J. Van 65: 193-195. Majerus, M. E. N., 2002. Moths. The New Naturalist. HarperCollins. Skinner, B., 1984. Colour identification guide to moths of the British Isles. Viking. Skou, R, Nordens Ugler. Apollo Books. Waring, P. & Townsend, M., 2003. Field Guide to the Moths of Great Britain and Ireland. British Wildlife Publishing. A Red Admiral Vanessa atalanta L. (Lep.: Satyridae) in London on the first of March At 13.00 hours on 1 March 2007 a Red Admiral Vanessa atalanta appeared in the sunny forecourt of our block of flats in Brixton, London. It landed at the foot of a tree and sunned itself for about ten minutes on the border between gravel and soil. It was a large female with considerable damage to the wings, including part of the hindwing that was still attached, flapping in the wind. This is a clear indication that it was a hibernating individual since any migrant this time of the year most likely would be in good condition. It is the first butterfly I have seen this year - not that Brixton is a famed for its butterflies. The day was sunny, but far from warm, and with a firm breeze. — Torben B. Larsen, 358 Coldharbour Lane, London SW9 8PL. 108 ENTOMOLOGISTS RECORD, VOL. 119 25.V.2007 Hummingbird Hawk-moth Macroglossum stellatarum (L.) (Lep.i Sphingidae) caterpillars in Banffshire On 18 July 2005 I visited the rocky sea cliffs at Tarlair (O.S grid reference NJ 7264), near Macduff in Banffshire. Some flourishing clumps of Lady’s Bedstraw Galium verum prompted me to search for caterpillars of Hummingbird Hawk-moth Macroglossum stellatarum, as immigrants had been reported elsewhere in Scotland earlier that summer. It seemed a very long shot, but within seconds I found an early fourth-instar caterpillar resting halfway up a bedstraw stem. Further searching was unsuccessful that day, but a week later I found three more caterpillars of this species in a steep, sunny hollow elsewhere on the site. These were also halfway up the bedstraw stems, fully exposed but well camouflaged by their green and yellow livery. Two were in their fourth instar and one its final instar. The range of sizes suggested they were the progeny of more than one female. Also found with them were eight caterpillars of Small Elephant Hawk-moth Deilephila porcellus, bearing out the comment in Pittaway (1993. The Hawkmoths of the Western Palearctic. Harley Books) that both species share similar larval habitat preferences. This seems to be the first time that Hummingbird Hawk-moth caterpillars have been found in Banffshire and indeed in North-east Scotland. If this is a consequence of global warming, then I for one am all in favour of it. — Roy Leverton, Whitewells, Ordiquhill, Comhill, Banffshire AB45 2HS. Diaperus boleti (L.) (CoL: Tenebrionidae) not confined to birch poly pore fungus The report of the large and distinctive beetle Diaperus boleti developing in birch polypore Piptoporus betulinus in Hatfield Forest, Essex (Piper, R. 2007. EnL Rec. 119: 74-75) is incorrect in implying that this is the sole host for the beetle. In The invertebrates of living and decaying timber in Britain and Ireland - a provisional annotated checklist (English Nature Research Report No. 467, 2002) I mention that this beetle has also been reported from dryad’s saddle Polyporus squamosus, and last autumn I found it in this fungus myself, also in Hatfield Forest, 17.x. 2006. This fungus causes pockets of decaying heartwood in a wide variety of trees - in this case an ancient beech. So Piper’s other comment that the beetle must be very sensitive to the volatile odours produced by birch polypore or the characteristic scent of birch wood ‘attacked’ by this saprophyte is also incorrect, as the beetle can develop in a variety of soft annual bracket fungi fruiting from a wide variety of broad-leaved trees. The key requirements for the beetle appear to be large fleshy brackets - suitably soft for larval feeding and suitably deep to hold a brood of developing larvae - in a well-lit situation where the warm sunshine will promote good development. - Keith N. A. Alexander, 59 Sweetbrier Lane, Heavitree, Exter EXl 3AQ. SERICOMYA HISPANICA IN FRANCE 109 SERICOMYIA HISPANICA PERIS, A LITTLE-KNOWN EUROPEAN HOVERFLY (DIP.; SYRPHIDAE) RECORDED FOR THE FIRST TIME FROM THE FRENCH PYRENEES Martin C. D. Speight Department of Zoology, Trinity College, Dublin 2, Ireland (E-mail: speightm@gmail.com) Abstract The occurrence of Sericomyia hispanica Peris, 1962 (Diptera: Syrphidae) is reported for the first time in France, from the Pyrenees. A key is provided to separate this species from existing British species. Introduction In Europe, the hoverfly genus Sericomyia comprises only a handfull of species, three of which {S. arctica Schirmer, S. jakutica (Stackelberg) and S. nigra Portschinsky) are northern European - subarctic, essentially - two others that are generally distributed and not infrequent and one that is southern European. The two that are generally distributed are the familiar S. lappona (L.) and S. silentis (Harris), for those working with syrphids in Britain or Ireland. The southern species is S. hispanica Peris, described relatively recently (Peris, 1962), but hardly referred to in literature since its description. The few existing records of S. hispanica are from localities scattered around mountainous parts of central (Peris, 1962) and northern (Marcos-Garcia, pers. comm.) Spain, but not the Pyrenees. Until now, no occurrences of this species have been cited for France. The present paper records S. hispanica from high in the Basque country on the French side of the Pyrenees, as follows: Pyrenees-Atlantiques: Foret dTraty, 8 June 1981, female, beside stream, old Fagus forest at 800m, coll, and det.MCDS, in colln. MCDS. In the field, S. hispanica is virtually indistinguishable from S. silentis and can be found in flight with that species. Under the microscope, the differences between S. hispanica and S. silentis are easily seen, including differences in the male terminalia (partially illustrated by Peris, 1962). The key to the separation of these three species provided by Peris (1962) seems to have been overlooked. Using keys like Nielsen (1997) or van Veen (2004), that do not mention S. hispanica, the species could easily be misidentified as S. lappona, due to the black tip to the abdomen that is found in both species. A modified version of the Peris (1962) key is presented below, to help draw attention to S. hispanica, and in the hope that it may bring to light further material of S. hispanica masquerading as one of the other species. The European Sericomyia species other than S. hispanica are keyed out by Nielsen (1997). 110 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 Key 1 Front femora entirely yellow (hypopygium black in male............. hispanica Peris tergite 5 entirely black in female; median black stripe on face ^ width of face) front femora partly black (especially basally and postero-laterally) and frequently predominantly black....... 2 2 Apex of abdomen black (hypopygium black in male, tergite ............ lappona (L.) 5 entirely black in female); median black stripe on face broad ( ^ width of face) apex of abdomen almost entirely yellow (hypopygium ................ silentis (Harris) yellow in male, tergite 5 yellow in female); median black stripe on face narrower ( ^ width of face) Discusssion Known larvae of Sericomyia species are of the characteristic “rat-tailed maggot” type, and live under the surface of water-logged (and often woody) plant debris. S. hispanica larvae presumably do likewise, in association with streams and flushes in the humid beech (Fagus) forest habitat in which the fly occurs. If so, there is no obvious reason why the range of S. hispanica should stop at the north-eastern edge of the Pyrenees and Sericomyia material derived from montane beech forest in other parts of the Pyrenees, or even further afield in southern Europe, might usefully be checked in case it includes this species. On that assumption I asked both Jean-Pierre Sarthou and Dave Levy, both of whom have collected syrphids in the Pyrenean beech forests, if they could check their Sericomyia material for S. hispanica. However this brought to light no further specimens and it is conceivable that the extremely “Atlantic” climate of the northern edge of the Pyrenees provides for the occurrence of S. hispanica at Iraty, but that further south the climate of this mountain chain is in some way inappropriate for it, over the altitudinal range that beech forests occur. By contrast, the closely similar S. silentis occurs from one end of the Pyrenees to the other, being found as close to the Mediterranean coast as the beech forests of the Foret de la Massane, that is located just inland of and uphill from Banyuls-sur-Mer. In the event that reading this note results in discovery of further material of S. hispanica, that extends the known range of the species, it is to be hoped that the records involved would be published. Alternatively, if their existence could be made known to the author of this note any new data they provide could be included in the StN database (see, for instance, Speight, 2006). Acknowledgements I am grateful to Maria-Angeles Marcos-Garcia for information about Sericomyia hispanica and to Santos Rojo for kindly providing me with a copy of Peris’s otherwise unobtainable paper on that species. My thanks are also due to Dave Levy and Jean-Pierre Sarthou, for taking the time to check through their Pyrenean Sericomyia material, in a hunt for S. hispanica specimens. SERICOMYA HISPANICA IN FRANCE 111 References Nielsen, T. R., 1997. The hoverfly genera Anasimyia Schiner, Helophilus Meigen, Parhelophilus Gerschner and Sericomyia Meigen in Norway (Diptera, Syrphidae). Fauna norv. Ser.B 44: 107- 122. Peris, S. V., 1962. Los Sericomyiinae de Espana con descripcion de una nueva especie de Sericomyia (Dipt. Syrphidae). BoL R.. Soc. Esp. Hist. Nat (B), 60: 55-60. Speight, M. C. D., 2006. Species accounts of European Syrphidae (Diptera), Ferrara 2006. In: Speight, M.C.D., Castella, E., Sarthou, J.-P. and Monteil, C. (eds.) Syrph the Net, the database of European Syrphidae, vol. 54, Syrph the Net publications, Dublin. Van Veen, M., 2004. Hoverflies of Northwest Europe: identification keys to the Syrphidae. KNNV Publishing, Utrecht. Coleophora involucrella (Chretien, 1905) (Lep.: Coleophoridae) : The second record for France A ten day visit to Sauliac-sur-Cele, in the Lot Department in south-central France at the end August and beginning of September 2006 saw several species of the handsome vibicella group of Coleophora come to mv and actinic lights positioned amongst scrub habitat on the edge of limestone cliffs which form the southern edge of the plateau de Gramat. One particular specimen had a wing span of 15mm and resembled C. conspicuella, but had the white subcostal streak appear to reach the costa at two-thirds then continue to the apex of the wing which threw some concern as to which species it may actually be - conspicuella normally stops at two-thirds. Back home and in the depths of winter I again had another look at this and decided to dissect, which threw up more questions as the male genitalia did not appear to resemble any of the British vibicella group depicted in volume 3 of Moths & Butterflies of Great Britain & Ireland (Harley Books), my only reference to this family. I therefore sought the advice of Giorgio Baldizzone (Asti, Italy) who was quick in his reply and named the moth as Coleophora involucrella, apparently the second record for France; the first was found in Languedoc during 2004 by J. Nel, who found two larval cases on Santolina chamaecyparissus in the Herault, at Puech de Grange, near to Nissan-les Enserune (Nel, J. & Varenne, T. 2004. Description de Bucculatrix pyrenaica species nova Microlepidopteres nouveaux pour la France (Lepidoptera, Bucculatricidae, Tineidae, Coleophoridae et Gelechiidae). Revue de r Association Roussillonnaise d’Entomologie 13: 114-117). Nel also observed the same species in the same condition in Spanish Cerdagne at Prats not far from the French border in 1992 suggesting this species can colonise new areas with ease if the food plant is present and therefore further records may be encounted in the near future. It is not certain though if the Sauliac specimen is from a local colony or if it is a migrant blown over the Pyrenees by the notorious Tramontane wind. The foodplant Santolina, commonly known as cotton-lavender, is a popular cultivar and grows in several gardens in the commune of Sauliac, including in one adjacent to where we ran the lights. The plant can re-seed very easily; it is a typical Mediterranean species, which copes well with drought. There is also a good colony 112 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 along the road near St Chels only a few kilometres away and this contains two of its varieties Santolina chamaecyparissus, and the greyer Santolina rosmarinifolia which has rosemary-like lobe-less leaves and appears naturalized there (Marian Clarke, Sebastien Billot, Association Sauliacoise d’Animation. Pers. Comm.). Coleophora involucrella was described from San Ildefonso, Spain and bred by Chretien from Santolina rosmarinifolia. The only Portuguese record is from the Lagoa de Santo Andre area, about 15 km N. of Sines, on the coast S. of Lisbon found by Martin Corley in 1998, with abundant cases on Santolina. (Corley, M.F.V., 2004. Provisional list of the Lepidoptera of Lagoa de Santo Andre, Baixo Alentejo, Portugal (Insecta: Lepidoptera). SHILAP. Revista de Lepidopterologia 32 (126): 105- 138). It appears also to be known from Morocco. Many thanks to Giorgio Baldizzone, Martin Corley, Martin Honey, Marian Clarke, Sebastien Billot, Mike & Brenda Marney, Robin Howard and Colin Plant for much discussion and help with this article. — Jon Clifton, Kestrel Cottage, Station Road, Hindolveston, Norfolk NR20 5DE (E-mail: jon.clifton@btinternet.com). A colony of Deltote bankiana (Fabr.) (Lep.: Noctuidae) persisting on a calcareous downland site in East Kent (VC 15) During the 1993 to 1995 period, I recorded small numbers of Deltote bankiana (Fabr.) on several occasions at a site on the outskirts of Dover, Kent {Ent Rec: 105: 288). This apparent colony occurred in atypical habitat for the species, in rough grassland towards the base of a south facing calcareous slope. This contrasted with the usual damp, marshy situations I had encountered this species previously, and with which all the other known breeding populations of this species in Britain are associated. At the time, it was felt this colony may have been established as a result of recent immigration, and was likely to be rather short-lived. Indeed, I failed to record D. bankiana on several casual visits to the site in the late 1990s and early 2000s. I was therefore interested to learn that this localised population was persisting until at least 2004, when David Burrows recorded four individuals on two visits to the site in June (DB and 1. D. Ferguson, pers. comm.). This was more surprising as the locality was inappropriately managed in the mid to late 1990s, when over- grazing significantly reduced sward height levels across the site and probably directly led to the demise of two other rare moth species that occurred in good numbers here prior to the grazing - Jordanita globulariae (Hb.) (Lep.: Zygaenidae) and Aspitates gilvaria (D. & S.) (Lep.: Geometridae): A cautionary tale about the need for familiarity with a site and its important faunal interests, and tailoring habitat management to suit. I am grateful to David Burrows for informing me of his records of D. bankiana, and to Ian Ferguson for confirming the details of these records. — Sean Clancy, 1 Myrtle Villas. Sussex Road, New Romney, Kent TN28 8DY. NOTES 113 Additional notable British barkfly (Psocoptera) observations This report summarises previously unpublished barkfly (outdoor Psocoptera) records from two sources: new observations made in 2005-6, and earlier records made by contributors to the newly launched national Psocoptera (outdoor species)/barkflies recording scheme (see BRC website - www.brc.ac.uk). KNAA made several notable finds while surveying sites in Northern Ireland in 2006 that will not be included in this paper. They will be published in the Irish Naturalists' Journal in due course. Amphipsocidae Kolbia qukquiliarum Bertkau Keith R Bland collected male and female specimens of this species in a malaise trap operating in dune slack grassland at Kilmory, Rum, Scotland (NG3603) between 27- 31.viii.2000. Charles Lienhard (Geneva Natural History Museum) confirmed the identification of the specimens. This species had previously been considered to be confined to southern England and its occurrence on a Scottish island shows that it has a far greater distribution range. KNAA also found some specimens by sweep-netting herb-rich mesotrophic grassland at Coombeshead Farm, Arlington (SS6619), North Devon, 21.vii.2005. Ectopsoddae Ectopsocus axillaris (Smithers) This recently established introduction appears to have rapidly spread across the country and is now regularly found amongst gorse and yew foliage, on aerial dead branches on open-grown trees, and other situations. It has been found by KNAA in: East Cornwall: Blisland (SX1075), 13.vi.2005; St Dominick (SX4167), 20.vii.2006; and Lansallos (SX1751), 24.viii.2006; West Gloucestershire: Brockweir (S05300), 6.vi.2006; Monmouthshire: Brynmawr (SO 19 12), 7.ix.2005, and Clydach Gorge NNR (S02212), 5.ix.2006; Worcestershire: Birlingham (S0929442); and County Durham: Waldridge Fell (NZ251489), 5.vii.2005. The species has also been found by RES in: Falkirk: Airth (NS897877), 15.V.2005; Lancashire: Marton Mere (SD3435), 17.vii.2005; Lincolnshire: Legbourne (TF367845), 23.vii.2006; and Fife: Kinghom (NT270868), 10.ix.2006. Peripsoddae Peripsocus alboguttatus (Dalman) RES collected a single female specimen from a goat willow Salix caprea bush in a small valley near Hartside in the Lammermuir Hills (NT474537 - vc81) on 14.viii.2006. A further search of the scattered bushes in this area of the valley bottom on 18.viii.2006 produced another female specimen, this time on grey sallow Salix cinerea. A short amount of time was also spent sweeping the rough grassland in the area but no specimens were found. This is the second Scottish site for the species. 114 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 Peripsocus milleri (TiOyard) We have previously reported on the first outdoor records of this species in 2005 (Saville, B, Alexander KNA, Dolling WR & Kirby P, Ent Rec 117: 35--39) but two earlier specimens have only recently come to light: KNAA has one from Walcot Park in Shropshire (S0345859), 8.viii.l996, and Moseley Green, West Gloucestershire (SO632086), 18.vii.l998. These records suggest that the species was already spreading across the west of England (at least) well before its presence was first appreciated in 2004. Further records have also been forthcoming and it is clearly now well-established across much of the southern half of England. KNAA found it at Duncombe Park NNR, North Yorkshire (SE6082), 28. vi. 2005 & 2.x. 2006; and Claverton, North Somerset (ST776645), 22.ix.2006. The majority of these records come from tapping aerial dead branches on old open-grown trees. Peripsocus parvulus Kolbe A female specimen was beaten from a small yew bush at the entrance to South Darley church, Derbyshire (SK267615) by RES on 31.vii.2006. Another site for the species was found the next day (two kilometres away). A total of 42 specimens were found on a row of oak trees edging a road near Stanton in Peak (SK252639). 24 males and 15 females were found on the trunks of the trees while one male and two females were found by beating the branches. As is usual with this species, all of the males were macropterous while all the females were brachypterous, KNAA also found two females in Cwm Clydach NNR, Monmouthshire (SO2212),5.ix.2006. There has only been one previous record of this species in Britain (McLachlan, R, 1890, Ent Mon Mag 26: 269-270) - McLachlan also found a substantial number together in the same area: about two dozen specimens on a paling on the outskirts of Lyndhurst, New Forest on 31,viii and l.ix.l890. He also reported finding macropterous males and brachypterous females though he also thought he had a number of macropterous females. Trichopsocidae Trichopsocus clarus (Banks) RES obtained one female specimen from elder/hawthom scrub at the northern end of Hunstanton cliff, Norfolk (TF679424) on 27.vii.2006. This is the second published record for England (Saville et al, loc.cit.). Trichopsocus brincki Badonnel One was found by KNAA at South Penquite Farm, Blisland, East Cornwall (SX1075), 22. vi. 2005, and Coombehead Farm, Arlington, North Devon (SS6139), 21.vii.2005. Two males were beaten from gorse on the open rough pastureland of Darren Ddu, Llanelly, Monmouthshire (SO223170), 4.ix.2006. Three females were beaten from a yew in South Darley churchyard, Derbyshire (SK267615) on 31.vii.2006 (the same bush that Peripsocus parvulus was recorded from) by RES. On 4.viii.2006 a further two females were found on an introduced NOTES 115 conifer along the roadside near North Britain (SK302649) about four kilometres from the first location. Twenty-seven cones of Douglas fir Pseudotsuga menziesii and spruce Picea sp., blown down in gales, were collected by JHB in Treborth Botanic Garden, Bangor (SH552710, vc49) on 3.xii.2006. They were kept indoors in a sandwich box at 10- l5°o C, and over the rest of the month four adults and one juvenile T. brincki were found among them, det. BS. This record is particular interesting since it suggests that the species may be capable of over- wintering as an adult. Our previous debate (Saville et al, loc.cit.) concerning whether this is an overlooked native or yet another recently establishing introduction appears to have been resolved. It is clearly rapidly spreading across the country. Elipsocidae Propsocus pulchripennis (Perkins) On 31.viii.2004 a visit by GMEO to the East Sussex SSSI/NNR at Newhaven’s undercliff resulted in the capture of three specimens of this very distinctive species. The site is a chalky place with rockfalls strewn around, often reaching to the shingle. Because of the presence of brambles, collecting with a net was ineffective, and a simple (transparent) plastic ‘sandwich’ box was used instead, hitting over the vegetation with the lid and seeing what fell into the box. The specimens were found in a rather small area of rank vegetation where the shingle meets the major vegetation (TQ448000): one specimen on a Chenopodium species (possibly Good King Henry), the other two on nettle. All the specimens have been housed in the Booth Museum, Brighton. This is the first record for mainland Britain, the only other records being from the Isles of Scilly (Saville et al, loc.cit.). Psoddae Psocus bipunctatus (Linnaeus) LC swept and beat several specimens from a lichen-encrusted Oak Quercus robur L. branch at Blaxland Farm, Broad Oak near Canterbury, Kent (TR161634) on 30.vii.2006. The identification of one of the specimens was confirmed by KNAA and RES. According to New (1974, 2005) this species had not been recorded in Britain since 1837. A further examination of the site on 9.ix.2006 revealed no further specimens. — R. (Bob) E. Saville, 20 Downfield Place, Edinburgh EH 11 2EL (Email: info@lothianwildlife.co.uk), Keith N. A. Alexander, 59 Sweetbrier Lane, Heavitree, Exeter EXl 3AQ (Email: keith.alexander@waitrose.com), John H. Bratton, 18 New Street, Menai Bridge, Anglesey LL59 5HN (Email: jhnbratton@yahoo.co.uk), Laurence Clemons, 14 St. John’s Avenue, Sittingboume, Kent ME 10 4NE and G. Marcus E. Oldheld, 33 Dene Vale, Brighton, East Sussex BNl 5ED (Email: Moldbug3@ntlworld,com) 116 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 Bloxworth Snout Hypena obsitalis (Hb.) (Lep.: Noctuidae) hibernating in German wartime bunkers on Guernsey and Alderney During the German wartime Occupation of Guernsey and Alderney from 1940“! 945 an enormous number of military fortifications, varying in size, complexity and purpose, were built all over both islands. On Guernsey, many still stand today. Some, such as those set mainly above ground on the cliffs, are enormous, with walls of two metres thick reinforced concrete, while others are underground and take the form of tunnels or much smaller bunkers. The entrances to these underground bunkers today are mainly overgrown, and more or less hidden from view, but inside they have withstood the march of time remarkably well showing little signs of wear, and they remain much as they must have been 60 years ago. But whereas during the Occupation they were used mainly to accommodate troops, or to store ammunition, today (those which are easily accessible) mainly contain just the signs of contemporary youthful activity, much of it illegal. They also contain hibernating Lepidoptera. Of these smaller underground bunkers, the ones the moths seem to favour are those which have several inner chambers, typically reached along a narrow corridor and around several bends, where the insects are not exposed to the elements. These bunkers are not necessarily dry, but they are not draughty, and they are absolutely dark. The species commonly found are the Herald Scoliopteryx libatrix, usually in small numbers; the Twenty-plume Moth Alucita hexadactyla, in much larger numbers; and the Bloxworth Snout Hypena obsitalis, which can sometimes be present literally in hundreds. On 8 February 1972 Rich Austin, now the Guernsey recorder, counted over 200 obsitalis in just a small part of the (currently inaccessible) Mirus battery (Carter, 1972, Ent. Gazette 23: 267) and on 4 March 1989 my wife Pat and I, while looking for bats, found 103 obsitalis in a tunnel which had once led to a searchlight higher up a cliff. On 2 February 2006, in this same tunnel, we found 68 obsitalis with 141 hexadactyla and 21 libatrix - but never any bats. The same is the case on Alderney where there are also many bunkers. David Wedd, an Alderney resident and frequent visitor to the other islands says: “I have found obsitalis in many bunkers, but only those where Pellitory-of-the-Wall Parietaria judaica grows around (or actually on) the outside walls, and for much of the year ova, larvae, pupae and moths can be found together. On Alderney they are particularly numerous in two bunkers at the edge of Longis Bay, where the Bloxworth Snout occurs along with hexadactyla and libatrix, but also the Peacock butterfly Inachis io, Small Tortoiseshell Aglais urticae, Satellite Eupsilia transversa and this winter a single Buttoned Snout Hypena rostralis. We have not disturbed the bunkers since this recent cold spell started, but until the New Year numerous obsitalis were fluttering outside in the evenings, and the ones inside were extremely mobile (whereas the other species were well into hibernation.) The occurrence of Bloxworth Snout to light is quite rare. During 2005-6 we have regularly run mv traps quite near to the bunkers, and have taken just one obsitalis at light, yet have watched the moths fluttering in numbers less than 50 metres away.” (Wedd, pers. comm.) NOTES 117 Following an exchange of e-mail messages on the ukmoths mailing list in which the over-wintering strategy of the Bloxworth Snout was discussed, three enthusiasts from the Midlands, Keith Tailby, Mark Hammond and Graham Finch, decided to visit Guernsey with a view to seeing and photographing them. Their plan was to fly from Birmingham, returning home the same day, and the early date chosen for their visit, 16 January 2007, would normally have been ideal. However, the last few winters here on Guernsey have been very mild, the present winter exceptionally so, with the nature correspondent of our local newspaper reporting that primroses, which normally bloom in time for Christmas here, had been in flower in his garden since 20 September, and early narcissi since mid-November. In early January, in preparation for the visit, and with daytime temperatures reaching 1 1 °C, Pat and I visited the five bunkers we had decided to show our visitors. We were dismayed to find that although one or two Bloxworth Snouts were present in each of four of them, in the searchlight tunnel there were just 23 albeit with 10 libatrix and numerous hexadactyla. This did not bode well especially when a week later, with daytime temperatures then reaching 15°C, another very brief visit found just 12 obsitalis. In near-desperation, fearing there would be none left at all, six were potted up, taken home and placed in the fridge. Fortunately, there were then several cold nights when temperatures dropped to 5°C and we were hopeful that no more moths would leave the bunker. But on the day, to our surprise, we found between 40 and 50 obsitalis - not only had they stopped leaving the bunker they had actually returned although, as David had observed on Alderney, they were skittish and easily disturbed, whereas the other species seemed unaffected by our presence. A further interesting observation had been made by Mark who commented that when he had disturbed a Bloxworth Snout in one of the other bunkers, it had flown into the dark rather than towards the daylight. So when I came to release the six potted specimens back into the searchlight tunnel I chose a point near the entrance where they could fly towards either the dark or the light - each chose to fly into the dark. The Bloxworth Snout is not uncommon in Guernsey although, as David has also found on Alderney, it rarely comes to light traps or lighted windows and is more often noticed hibernating in sheds and greenhouses. The moth was first recorded on Guernsey in the autumn of 1962, and then again in the autumn of 1963, and although presumably the latter could have been fresh arrivals, had they been locally-bred then their parents would have survived the exceptionally severe winter here when temperatures fell in January 1963 to - 8°C {Transactions of La Societe Guernesiaise 1962, 1963). How could a species which is almost at the northern limit of its range, and which over-winters as an adult, have survived such conditions? Taylor has described seeing the Tissue Triphosa dubitata hibernating in a cave in Breconshire in which the temperature at the time was 10 - 13°C and which he felt probably varies very little from this (1979. Ent. Rec. 91. 173 -174). And in a detailed study of dubitata and libatrix hibernating in a partly-subterranean Victorian fort at Box Hill in Surrey, Morris and Collins found that during the study period of November to April, although the external temperature varied from -4°C to +22°C, the internal 118 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 temperature was always in the range 2 - 6°C (1991. Ent Rec.\^3: 313-321). Some of the underground bunkers are enormous - the Mirus battery is large enough to have accommodated almost 300 men - and many are now on private land where they are inaccessible and lie undisturbed. Perhaps those early arrivals survived the winter by retreating deep into the heart of these large structures? I am grateful to David Wedd for allowing me to reprint verbatim his response to my request for information and for his helpful comments on this note.- P. D. M. CosTEN, La Broderie, La Claire Mare, St. Peters, Guernsey GY7 9QA. (E-mail: pcosten@guemsey.net ) Hazards of butterfly collecting: Paragliding butterflies - Ghana 2007 Throughout February 2007, a huge butterfly migration flew south-southeast from northern Kenya towards Tanzania. It was wholly composed of a single species, the Common Caper White Belenois aurota Fabricius. Such migrations are frequent in East Africa, but it gradually became clear that this was an exceptionally big event. Together with James Wolstencraft in Tanzania, I somehow became information coordinator on this event and we share a file of some 400 e-mails on the matter, ranging from brief, single observations to painstaking attempts at establishing a maximum number of facts about the size intensity and nature of the event. We have not yet analyzed the data. I really look forward to having a huge map of East Africa on the floor of my flat with little flags showing the data from each of the many observations. It will look a bit like the “operations room” in countless films about the 'Battle of Britain’ during World War II. I am a rather cautious person, but I hazard the guess that more than 100 million individuals were involved [watch this space]. Among all this correspondence came a - self-admittedly irrelevant - bit of information from Kuruman in South Africa. One Walter Neser wrote that while he was paragliding at 1,000 metres he had seen many white butterflies flying in the thermal together with the vultures that he was trying to photograph. The following e- mails were exchanged during February /March: Larsen (TBL) to Neser (WN): “This obviously has nothing to do with the East African migration, but it would be of great interest if any of your pictures are of sufficient resolution to identify the butterflies in question.” WN to TBL: “My parents know butterflies well . . . they might be able to make an identification.” TBL to WN: “If they can, we should do a joint paper for Metamorphosis, the journal of the South African Lepidopterists’ Society.” WN to TBL: “OK ... I am in Ghana at the moment and will be traveling a lot, so it may be a while.” NOTES 119 TBL to WN: “Amazing, Fll be studying butterflies at Bobiri in Ghana during much of March and April. You must try to visit there. I heard some rumours about paragliding at Nkawkaw which is not far from Bobiri. You involved with that? WN to TBL: “Yes ... we are flying at Nkawkaw 5 to 10 April. Come along and you can have a ride. I am actually passing Bobiri just now, but have no time to stop. Call me on my Ghana mobile.” TBL to WN: “Fll be arriving Bobiri with two friends - 7 April seems suitable. I always wanted to try a paraglider. It would be great if it were to happen.” I was staying in the Bobiri Butterfly Sanctuary for several weeks to continue a butterfly census that will also act as a baseline for a comparative survey to be conducted between 2090 and 2100 to study potential long-term changes in butterfly biodiversity. Of particular interest is whether forest fragmentation has led to an ‘extinction debt’ that remains to reveal itself. The effects of climate change may also change the composition of the butterfly fauna, which would be an interesting and important issue to study. Finally, the possibility that Bobiri itself will be degraded by human activity cannot be ruled out; the effects of that would be significant as well. Those of us involved in the present survey will probably not be around in 2090-2100 - but King, the kind security guard at the Bobiri guest house, put it well: “But your souls will be there!” Bobiri is a nice forest and nice forests are usually not within the range of Ghana’s burgeoning cell-phone range, so on 6 April I went off to the neighbouring village to call Walter. He came over loud and clear: “Come tomorrow to Hotel Rojo in Nkawkaw before nine. Then we can have some breakfast before going up the mountain for launch. You can fly with me a couple of hours later when the thermals are usually best.” It is worth looking at the probability, or rather improbability, of the sequence of events related in the above: WN posting his observation on that specific migration website - 100:1. TBL responding to this - 10:1. WN being in Ghana and saying so in the reply e-mail - 100-1. TBL guessing that he had something to do with the events in Nkawkaw - 10:1. TBL being in Ghana at the time - 10:1. I am being quite modest in assigning these probabilities: they nonetheless add up to a total improbability of ten million to one - surely enough reason in itself to go and give paragliding a try. So we met at Hotel Rojo and Walter turned out to be a very nice man with huge responsibilities. He was actually coordinating a ‘paragliding festival’ together with the Ghana Ministry of Tourism. At the breakfast table were seventeen invited glider pilots from all over the world and an array of journalists from the vigorous Ghanaian press: all part of putting Ghana on the world tourism map in a more exciting way [some might say!] than watching butterflies in the Bobiri Butterfly Sanctuary. At 09.00 hrs we set off for the launch site on the magnificent Akwapim Escarpment. Walter believes it to be one of the best paragliding localities in the world. The drop to the designated landing field is only about 450 metres, but this is redeemed by a steady supply of thermals that allow the gliders to stay up for long periods - the day before someone managed to be airborne for more than six hours. A 120 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 happy audience was already present. The Minister of Tourism arrived; I think he was a bit unhappy that the cabinet had previously decided that it would not be ‘appropriate’ for him to fly, but he did add gravity to the event. Gliders were unpacked from oversized backpacks and pilots began to take off. Three of four bounds down the take-off ramp yanks up the wing, and when the wind takes hold, almost unbelievably up goes the tiny, fragile structure. There is a similarity with a butterfly take-off, though no flapping of wings is necessary; a paraglider cruises at about 35 km per hour, less than the large Charaxes-huii&dXit^ at the launch site can do. My own take-off, with Walter as the pilot, was less elegant than I might have wished for. A slight reversal of wind stalled our take-off - I stumbled and was dragged along the ground for a few metres, though we were actually more-or-less airborne. It looked more dramatic than it was but I was cheered by the audience applause when we were airborne fractions of a second later. Walter had noticed small black butterflies migrating just above the scarp (almost certainly the African Beak Libythea labdaca, but the thermals were not friendly and we could not get high enough. The butterfly net I had brought never came into use. We had a wonderful flight. The passenger is hooked onto the pilot and sits right in front of the glider; you do not even see your own feet when looking straight down. Noise from the ‘wing’ above you is so low that you hear sounds from the ground below and ‘cockpit conversation’ is easy. We did find a few thermals thanks to circling vultures, but they were not strong, and all good things come to an end. We landed safely on a designated football pitch just in front of the Rojo Hotel - a ‘dust-devil’ on landing gave a bit of unwanted lift so we had to drag the gear somewhat longer than we really wanted. The result of the improbability of one to ten million of our e-mail correspondence, ended up being one of my most exciting days since my one and only parachute jump some 25 years ago. It really is great to do ‘something completely different’ at the age of 63. If you go to Ghana a few years from now there will probably be competent Ghanaian pilots who can take you for a ride - do let them. And keep your eyes skinned for migrating butterflies! — Torben B. Larsen, UNDP Vietnam, c/o Palais des Nations, 1211 Geneva 10, Switzerland. Nothing between you and the ground. You cannot even see your own feet. But, on this occasion, also no butterflies NOTES 121 Xanthia icteritia Hufn. (Lep.: Noctuidae): A comment on infraspecific variation, especially in regard to Kent This formerly very common species although appearing in county and other lists is rarely afforded detail, or even mention, of its infraspecific forms. Tutt (1892. The British Noctuae and their Varieties) gives an excellent account of eight forms in two parallel series based upon their ground colour and an abridged version of this appears in Heath et al (1983. The Moths and Butterflies of Great Britain and Ireland). Chalmers-Hunt (1966. The butterflies and moths of Kent) has very little to contribute, noting that ab. flavescens Esp. is widely distributed in the county, and that ab. cerago Hb., ab. aurantia Tutt and ab. imperfecta Tutt from Kent are represented in the National (RCK) Collection. Until quite recent times the collecting of a plastic bag of sallow catkins would be rewarded in due course, and with little attention, with an abundance of X. icteritia, and a few of other species of moths. Such collections, especially when repeated in the same locality for several years, give an accurate assessment of the composition of the local X. icteritia population. To-day, at least in Kent, this operation brings little reward. In north-west Kent the two commonest forms have been ab. fulvago L. and ab. aurantia, the penultimate members in depth of markings in the two series, by use of this method. Considerably less common are the two lightly marked forms, ab. cerago and ab. imperfecta while ab. flavescens and ab. obsoleta Tutt are of regular, but of only occasional occurrence. In my collection I have one specimen of ab. suffusa, bred from Swanscombe 30.viii.l951; I have not encountered ab. virgata, in north-west Kent or elsewhere, and this would seem to be rare throughout the species’ range in the British Isles. The identification of moths which fall into two distinct dines presents difficulty, and to minimise this I have used the following scheme which is a simplification of the descriptions of the varieties as given In Tutt 1892: ab. cerago and ab. imperfecta have some reddish markings on the forewings, but they do not coalesce to form a transverse band. ab. fulvago and ab. aurantia have a definite, somewhat ragged fascia which usually bifurcates towards the costa to include the reniform stigma. ab. suffusa and ab. virgata are heavily marked with the central band and its branch to include the reniform stigma. This fascia is well defined and solid. It is more extensive than that of X. togata Esp. and is broader on the costa; X. togata tends to have the reniform stigma free. In north-west Kent, apart from the two most heavily marked forms, in most counts the yellow varieties have slightly outnumbered the orange forms, and recent garden mv light records have confirmed this trend. However, there appears to be evidence that this slight imbalance does not prevail throughout the British Isles. Barrett (1899. The Lepidoptera of the British Islands, p.363) describes the species as being pale yellow, and later, under the heading of variation, states that in southern woods specimens may have the ground colour ochreous or orange-yellow. Barrett also 122 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 states that ab. flavescens (and he emphasises the pale yellow ground colour), is found more often in northern localities. In 1987, sallow catkins collected at Pontoon, Co. Mayo, produced a few X. icteritia larvae from which a dozen moths were bred, the majority of which were ab. cerago and the remainder ab. fulyago - a small sample, all v/ith yellow ground colour and the majority lightly marked. The catkins were collected from small bushes over a limited area. Nevertheless, despite the small sample, it is sufficiently interesting to suggest that X. icteritia in Ireland is worthy of study. Baines (1964. A Revised Catalogue of Irish Lepidoptera. p.40) does not include Co. Mayo in his list of counties in which X. icteritia has been recorded. — B, K. West, 36 Briar Road, Dartford, Kent DAS 2HM. MOTHS COUNT and the National Moth Recording Scheme - an update The Moths Count: National Moth Recording Scheme project is now officially up and running, having been launched by Sir David Attenborough on 2 May 2007. Moths Count is the name given to the whole project, which includes many training and awareness raising activities alongside the core aim of setting up a long-term National Moth Recording Scheme (NMRS) covering macro-moths in the UK, Isle of Man and Channel Islands. The project is a partnership of many national and local organisations, businesses and individuals, led by Butterfly Conservation. The project team consists of Richard Fox (Project Manager), Les Hill (Database Manager), Zoe Randle (Moth Recording Co-ordinator), Susan Anders (Outreach Officer) and Sarah- Ann Boon (Project Assistant). The team is based at Butterfly Conservation’s Head Office at East Lulworth, Dorset. The purpose of Moths Count is to widen the appeal of moths and moth recording throughout the UK and to establish an ongoing recording scheme for the 900 plus species of macro-moths. The resulting dataset is likely to be one of the largest biological datasets in the world. Recent research has highlighted the decline of many species of moths that were once common and widespread. The data collected from this project can ultimately be used to improve knowledge and understanding of moths and the changing distribution and status of each species and to inform effective biodiversity conservation and sympathetic land use policies. Zoe Randle will be working with County Moth Recorders, local moth groups, Butterfly Conservation Branches and other organisations to develop the NMRS and to strengthen the important support network for new and existing moth recorders. This will be achieved by recruiting volunteers where there are currently no or few moth recorders; providing training opportunities as appropriate; supporting County Moth Recorders and filling gaps in the vice-county network. The NMRS database will be up and running during the summer, at which point we hope that County Moth Recorders will be willing to provide copies of their local data to create the ‘national’ data set. Les Hill will provide technical assistance in the interchange of data between the National Scheme and County Moth Recorders. NOTES 123 Specialist training workshops are being organised for existing moth recorders to enhance their skills. These will include identification of critical species; surveys of rare species; working with the media; planning and organising pubic events and using computers to manage moth records. Feedback and useful information for moth recorders is an integral part of the project. The NMRS will only be a success with the support of moth recorders. Annual newsletters, online provisional distribution maps and training and public event listings will be available on the project website (www.mothscount.org) in due course. Aside from developing and running the National Moth Recording Scheme, the Moths Count project plans to encourage a greater appreciation and enthusiasm for moths among a new, wider audience. This will be achieved in a number of ways, not least by working to get positive coverage of moths in the media. One new event will be an online, annual ‘citizen science’ Garden Moth Count, which will encourage members of the public to look for and report easily-identified moths such as the Humming-bird Hawk-moth. The Garden Moth Count will be taking place from Friday 22 June to Sunday 24 June 2007; this is in addition to National Moth Night, which is planned for Saturday 1 1 August this year. Many other public participation events have been planned this year, in partnership with the moth recording community and partner organisations. How can you take part in the National Moth Recording Scheme? Simply continue to (or start to) send all your moth records to your County Moth Recorder. If you have other questions or would like to join the project mailing list, please contact Sarah- Ann Boon (saboon@butterfly-conservation.org). — ZoE Randle, Butterfly Conservation, Manor Yard, East Lulworth, Wareham, Dorset BH20 5QB Scotch Annulet Gnophos obfuscatus (D. & S.) (Lep.: Geometridae) on a pebble beach On the night of 19/20 July 2006, Jeff Waddell and I visited a previously un worked area of Lossie Forest on the Moray coast at O.S grid reference NJ 3166. The coastal strip here consists of successive parallel pebble beaches, none more than a few metres high, the oldest now over half a kilometre inland. Some are partially vegetated, being of botanical as well as geological interest. While working the low and level strip just inland of the present beach with torch and net well after dark, I was surprised to encounter at least six Scotch Annulet Gnophos obfuscatus flying gently over the pebbles and sparse vegetation. All were males in pristine condition as if newly emerged. This species is normally associated with inland crags, gullies, scree slopes and quarries, but there was no such habitat at the site or anywhere in the surrounding area. Presumably the extensive pebble beaches fulfilled its need for exposed bare rock, albeit in this case horizontal rather than vertical. — Roy Leverton, Whitewells, Ordiquhill, Comhill, Banffshire AB45 2HS. 124 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 News on the conservation of some moths listed in the UK Biodiversity Action Plan and two additional British Red Data Book species The aim of this article is to report the main high-lights of the conservation work on UK Biodiversity Action Plan priority species during 2006, and also the Silurian moth Eriopygodes imbecilla which has twice been proposed for inclusion as a priority species, and the Scarce Hook-tip Sabra harpagula, a Red Data Book species (Shirt, D, ed., 1987, Nature Conservancy Council, Peterborough). This follows in the foot-steps of similar annual reviews since 2000 (see Ent. Rec 113: 121-129 (for 2000), 114: 149-153 (for 2001) 115: 213-219 (for 2002), 116: 134-137 (for 2003), 117: 111-124 (for 2004) and 118: 211-218 (for 2005)). Barberry Carpet Pareulype berberata (D. & S.) During fieldwork in 2006, I was joined by Kelly Thomas, Moth Conservation Officer for Butterfly Conservation. Some funding for this and for Kelly’s involvement was provided by the BC Action for Threatened Moths Project. We were also invited to inspect and advise on a project in which the Veterinary Laboratory Agency (VLA) of DEFRA have planted over 500 Barberry plants near to the traditional site for the Barberry Carpet at Bury St Edmunds, Suffolk, with the VLA covering our costs. Additional survey work also took place by others in Oxfordshire and Dorset, with positive results at both known breeding sites. The key observations and developments in 2006 are as follows: The first generation of larvae started a little later than in recent years, due no doubt to the cold weather throughout April which will have delayed the emergence of the adults in May. In recent seasons mid June has been the time to start monitoring both the native populations and the establishment sites for larvae. However a brief check of the establishment site in Northamptonshire on 12 June produced no larvae and those of the Scarce Tissue Rheumaptera cervinalis, which also feeds on Barberry Berberis vulgaris, were all substantially less than 1cm in length, another indication of the lateness of the season in comparison with recent years. Kelly’s first sessions with me were therefore arranged for 28 & 29 June. I am delighted to say that on 28 June we found plenty of larvae at the Northamptonshire site, of all sizes. On 29 June our inspection of the VLA site showed that neither the site nor the hedges on its boundaries contain any well-established Barberry bushes so there will be no resident population on the site. Of the 500 new Barberry plants, which were installed in April 2006, a proportion were showing severe symptoms of drought and frequent watering was going to be required to keep the rest alive through the growing season. If this is done, this fenced site will provide a safe and promising location for establishing a population of the moth in a few years time. We beat and searched for larvae at the traditional and historic native site the same day and also at one of three sites where larvae have been released over the years as part of official attempts to establish additional populations in Suffolk. The good news is that we found Barberry Carpet larvae distributed throughout the establishment site we examined. In all previous visits since this establishment trial was started, with the NOTES 125 release of 450 larvae in 2000 and 220 larvae in 2001, the subsequent generations of larvae have seemed to be restricted to just a few of the Barberry bushes at the east end of the site, so it is excellent news to find they are now colonised the whole of it, from one end to the other. The bad news is that we found no larvae at all at the historic site, where the last record, despite almost annual beating, is of a single adult on 26 May 1995. Neighbouring land-owners are now pressing Natural England to denotify the site, which is an SSSI on account of the moth and its long history there - it was first discovered present in the 1860s. There are proposals to build houses on the open farm fields right up to the Barberry hedges. In my view the SSSI should be retained because the site remains of scientific interest as the only site in Britain where the moth has been known to have survived continuously for over 130 years. The population was decimated by two fires during the larval stage in 1991, from which it never properly recovered. We now have the knowledge to restore the moth to this site and hopefully we will have the opportunity to do this. Two clumps of Barberry in a farm hedge at Burwell, Suffolk, and four clumps in a hedge near Snailwell, Suffolk, were also beaten on 29 June, with negative results for both Barberry Carpet and Scarce Tissue, On 5 September I was joined by both Kelly and Marc Taylor (Moth Officer for the Wiltshire Branch of Butterfly Conservation), to check some of the known sites in Gloucestershire (one native site) and Wiltshire (where we inspected five native populations, representing two metapopulations, and also one translocation site). Some other known sites in north Wiltshire had already been inspected for larvae by Andy Foster with Kelly, on 22 August with positive results, and Andy had captured an adult in his garden light-trap on 6 August. We found a high density of larvae at the Gloucestershire site - five larvae, ranging from second to final instar, from a single spot on the main bush - i.e. just enough of the plant to cover one Bignell beating tray. We also obtained two Barberry Carpet larvae from young bushes now 1.5”2m tall which we have planted by the main bush, confirming again, as on previous occasions, that the females will lay on and colonise these. However, we found no larvae yet on young plants about 1.5m tall now established at the Northamptonshire and by an occupied bush near Ashley, Wiltshire. We also found high densities of larvae at all three sub-sites of the more southern meta-population in Wiltshire, with some larvae seen basking on the upper surfaces of leaves in the warm, humid but overcast weather. Pleasingly, the hedges at none of these had been flailed so far this year. Provided they were not flailed for three weeks thereafter, all the larvae would have had the chance to pupate without interruption. Volunteers Godfrey and Michael Smith monitored the very successful establishment trial near Trowbridge, Wiltshire, and once again found larvae throughout this extensive system of hedgerows. At the tranlocation site to the north of all these, both the transplanted Barberry bushes and the young plants established around them, have grown really well and now form a thick linear clump, with additional planting proposed for 2007. However, as in 2005, no larvae were found on either, nor at the original donor site nearby, despite beatings by John Grearson. This is a site the author would like to inspect more closely for larvae in 2007. The good news here is that there is local 126 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 interest in planting more Barberry, supporting additional monitoring, and that there may even be additional well-established Barberry bushes in the area which could be supporting the moth (Gareth Harris, pers. comm.). Following our session together, Kelly had a positive result at the single known site in Dorset where supplementary planting of additional Barberry has been successful. Kelly and Mark Warn (Forestry Commission, England) found a single final instar larva there on 7 September, confirming the continuing presence of the moth, which is highly localised here and currently at a low population density relative to many of the other known sites. Kelly also visited the Oxfordshire site on 10 July 2006 with Christopher and Stephanie Carter and Dan Hoare (BC, London & South-east Regional Officer), and they were lucky to find a late larva of the first generation. Larvae were first found at this site in 2005, following the chance capture of two adults nearby in 2004 (see Ent. Rec. 117: 252). The establishment site in Lincolnshire was not inspected for larvae in 2006, but produced a positive result in 2005 (see Lincolnshire Naturalist 26: 78-79) and will be examined in 2007. Many Barberry plants are being grown in various places to increase the numbers of planting schemes now underway to support future populations of this moth. In 2006, for the first time, Polly Jones, Plant Propagator at Westonbirt Arboretum, has been experimenting with “air-pots”, which encourage rooting, with much success. Black-veined Moth Siona lineata (Scop.) 2006 was first year since 1987 that the author did not visit the five key sites for this species, all of which are in Kent. From one of these the species appears to have been lost due to unfavourable habitat management dating back to a mowing incident in February 2001 (see Ent, Rec. 118: 212). There were no further records of the moth from this site in 2006, which was included in a monitoring programme conducted by Sean Clancy as part of the BC Action for Threatened Moths Project. Efforts are being made to return the site to a suitable state for the moth, with a view to natural recolonisation or establishment of a new population. The good news is that a sixth site, adjacent to one of the four occupied sites, appears to have been colonised. The site has been restored from scrub to herb-rich, mid-succession, open chalk grassland over the last decade as a result of work by the Kent Wildlife Trust and Kentish Stour Project, with many partners and supporters. A total of five adult moths was recorded by Sean on two dates in June 2006. These are the first records for the site since it became overgrown with scrub in the mid-1980s. To facilitate natural colonisation from the adjacent occupied site, a corridor of open ground was cut through a belt of woodland separating the two, with this work beginning three years ago, with additional clearance subsequently. Discovery in 2005 of the colonisation of the fifth site was reported in Ent. Rec. 118: 212, British Wildlife 17: 53-54 and in Br. J. ent, Nat. Hist. 19: 139-144. Monitoring in 2006 shows that numbers have been maintained at this site and at the three sites with surviving longer established populations of the moth numbers in 2006 were slightly above the average for recent years. NOTES 127 Four-spotted Moth Tyta luctuosa (D. & S.) As in previous years, the Four-spotted Moth was recorded at its handful of major breeding sites in England, and as a few scattered individuals elsewhere in southern England. One of the major breeding sites, at Peterborough, Cambridgeshire (in the Vice-county of Northamptonshire), was monitored by the author weekly throughout the summer, from early May to late August, as it has been every year since 2000, with funding from Peterborough City Council, Cambridgeshire County Council and the Environment Agency. The results are used not only to gauge the effects of habitat management work on the site, but also to advise and train volunteer surveyors and others who are searching for, or maintaining, populations on other sites. The spring of 2006 proved to be a late one. The adult moths appeared later than in any of the previous five years and were five weeks later than in 2003. None were observed until 6 June. Other observers in Cambridgeshire and Essex, including Phil Jenner and Sharon Hearle, reported not seeing their first ones in other populations until the weekend of 3-4 June. Only after these sightings was the green light sent out to surveyors to begin searches elsewhere. At the Peterborough site the numbers of adults seen on the 1.1 km (0.69 miles) transect route during the flight season of the first generation (14 individuals) were smaller than in any of the previous six years (highest 120 in 2004), but this was probably a response to the fact that the sward vegetation here became increasingly rank between 2004 and the summer of 2006 as a result of lack of management, rather than being a more general trend related to weather. The last of the first generation were seen on 28 June, a very short flight season compared to previous years, when it has extended into the first, half of July. On 21 July the first of a second generation was seen and on 28 July five separate adults were observed. This is the largest single day count for the second generation at this site since walking the transect began in 2000. Another adult, the last of the year, was seen on 3 August, with zero counts on 11 & 16 August. The previous largest total count in the second generation was four individuals in 2002 and the previous highest day count was 3 on 24 July in that year. Clearly the prolonged very hot weather in 2006 arrived at just the right time for plenty of the larvae to produce summer adults, despite the low numbers and exceptionally late emergence of the first generation Whether this has been a useful strategy, or has led to the wasting of some of an already declined population will be seen in 2007. Fortunately, I can report that in the week between my visits on 3 & 11 August 2006 the key dyke bank on which much of the breeding occurs was scraped of most of the vegetation, including the woody plants which had begun to flourish, by a team from the Environment Agency workforce. This operation, which took place almost annually up to 2004, maintains the hot, dry microhabitat and sparser which seem to suit the Four-spotted moth and its larval foodplant, so the adults flying in 2007 should find the habitat in a substantially more favourable condition than in the previous two years. After dark on 28 June, Kelly Thomas and I visited the known breeding grounds in Lincolnshire, where we searched for and found five larvae between 22.40 and 23.20 hours. The first four larvae were found quickly, between 22.40 and 23.00 hours, in a 128 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 favoured spot by a small former quarry at the west end of the valley, and the fifth when searching at the other end of the valley, confirming that larvae were distributed throughout the length of the south-facing side of this valley, as in previous years. The larvae ranged in size from L5-4cm and were found on the newer leaves of Field Bindweed Convolvulus arvensis in a sparse grass sward only 15-20cm tall. The first larva at each spot was found after only 1-2 minutes of searching. We then returned to the Peterborough site where we spent 30 minutes searching, from 00.15 to 00.45 hours, without finding any larvae. The caterpillars are clearly at a much lower density here, where the sward is substantially longer and lusher, partly as a result of lack of any cutting or grazing in 2004 and 2005. The author has been advising Carl Bro, Anglian Water and the Environment Agency concerning the impact of a plan to replace and reroute a major water main at the Peterborough breeding site. Paul Clack, Senior Ecologist for Carl Bro, Dodie Honisett, Design Team Leader, and Tichatonga Mhlanga, Design Engineer, for One Alliance and Cameron Hutchinson, Construction Manager for Balfour Beatty and the author met up on site on 25 October, with maps of the plans, to discuss the construction work. The good news is that the proposed work should not effect the known breeding areas, and may result in an increase in breeding opportunities by creating bare ground on which the larval foodplant should thrive. The author will be monitoring this during 2007 and reporting back to the above and to BC. The author also worked with Jane Ellis (BC, Midlands Brownfield Sites Officer), on a training event for volunteer Lepidoptera surveyors, which involved a visit to the Peterborough site on 6 June, and with Sharon Hearle (BC, East of England Regional Officer), during 2006 to conduct surveys and training workshops at the Kirtling Weirs and Great Wilbraham areas of Cambridgeshire and at some potential sites near to occupied areas in the vicinity of the extensive Littlebury population in Essex. On 6 June the training party saw four adult Four-spotted moths, an immaculate adult of the nationally scarce tortricoid Commophila aeneana and three individuals of the Grizzled Skipper butterfly Pyrgus malvae at the Peterborough site. All three species are now considered scarce in the region. On 14 June we located promising habitat for the Four-spotted moth at the Kirtling Weirs and saw four adult Four-spotted moths at Great Wilbraham. Returning for night-time searches for caterpillars, we found four Four-spotted moth larvae, froml.5-4cm, all within 50cm of each other, on green Field Bindweed foliage amongst sparse dry brown grass on a fence-line at Great Wilbraham at 23.15hrs on 4 July and one larva at the Kirtling weirs site at 00.45hrs on 5 July. These are almost certainly the first larval records for vice-county Cambridgeshire, at least in modern times. Proposed site work in the vicinity of Kirtling weirs is expected to increase the supply of suitable habitat during the next few years. On 2 August we searched the additional Littlebury sites by day for second generation adults, without success. However, the weather had suddenly turned cold and dull. The moth was still flying at the Peterborough site on 3 August, as noted above. The author will be conducting more workshops during 2007 to train and enable volunteers to assist in the surveying and monitoring this species for the newly NOTES 129 launched National Moth Recording Scheme. He would like to acknowledge the help of all the above-named individuals and organisations, and thanks the organisations for funding the various aspects of the work. He also thanks all the volunteers who attended the various events and wishes them well in locating additional populations of the Four-spotted moth in 2007. Marsh Moth Athetis pallustris (Hb.) Both the remaining known sites in Great Britain for the Marsh Moth were monitored for adults by light-trapping in 2006. Fearing that a planned light-trapping session to monitor the species at Saltfleetby National Nature Reserve on 25 May might be too early to see them this year, I moved the date to 31 May. This proved disastrous. Toby Ludlow who could not get to the revised date went on 26 May and recorded 14 in one light-trap. On 3 1 May, four of us, with eight traps, had a very cold night, with the minimum temperature falling to minus 2°C and we saw nothing of the moth and had only small catches of other species. At the other site, Gibraltar Point National Nature Reserve , also on the Lincolnshire coast and some 35 km to the south, a single Marsh Moth was captured on 10 June 2006 (Paul Troake), for the second year running. Interestingly, this male was captured in a light-trap operated within the one area of woodland and plantation on the site, where there are some open grassy glades. The previous one, a male, on 5 June 2005 (also trapped by Paul Troake) was at the north end of Freshwater Marsh in an area called The Measures, which contains the line of an old railway track and is otherwise a mix of dry grassland with scrub and dune-slacks, rather like the breeding areas at the Saltfleetby NNR. These moths are the first two seen at Gibraltar Point since 17 May 1997 when one was recorded at a light-trap on the edge of the reserve in Aylmer Avenue, by Kevin Wilson, Site Manager for the Gibraltar Point reserve (for the Lincolnshire Wildlife Trust). During the 1970s the Marsh Moth was widespread and fairly frequent at both sites. See Ent. Rec. 118: 132-134 for more information. The litter-pile technique was used to monitor the larvae again in 2006, this time at three places on the Saltfleetby reserve and near Freshwater Marsh at Gibraltar Point. This monitoring started on 30 September and 1 October in 2006 and was continued and completed on 8 October 2006. No Marsh Moth larvae were found in the twenty-two litter-piles constructed to sample the traditional collecting grounds on the Saltfleetby NNR, when the piles were searched on 8 October. In stark contrast, a total of 82 Marsh Moth larvae was found in the 20 litter-piles in the central part of the reserve which has only been surveyed in detail in the last three years. This total is over twice as many as the 40 from 24 piles there in 2005 and raises the estimate for the minimum density of Marsh Moth larvae in this area of dune grassland in 2006 to between 500 and 600 larvae per hectare or about one per 20ml No Marsh Moth larvae were found in nine piles constructed in nearby ranker grassland nearer to the coast, sifted on 30 September and 8 October, nor in eight piles constructed at the seaward end of Mere Meadow at Gibraltar Point and sifted on 1 October. 130 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 The Marsh Moth was the subject of a 15 minute feature filmed for television on 14 September 2006 on site at the Saltfleetby-Theddlethorpe Dunes NNR in Lincolnshire, for broadcast by the BBC in the summer of 2007. Reddish Buff Acosmetia caliginosa (Hbn.) After many years of survey, this species is only currently being monitored in the adult stage on one part of its complex single known British locality, on the Isle of Wight. Various key spots were suctioned-sampled for larvae during a brief visit by Kelly Thomas and Dan Hoare in 2006. Larvae were found in the expected places. I visited all the breeding areas in August and I was pleased to see that habitat management work by the Hampshire and Isle of Wight Wildlife Trust and partners, particularly the control of scrub regrowth and the selective clearance of some additional stands of scrub, is managing to keep pace with natural plant succession and maintain breeding areas of open, heathy sward, rich in Saw-wort Serratula tinctoria, the sole larval foodplant. I have often reported the benefits for other species of this work to maintain te last British population of the Reddish Buff. Some of the many other species of Lepidoptera which are benefiting include the Kent Black Arches Meganola albula and the Small Pearl-bordered Fritillary Boloria selene. The local population of Adders Vipera berus is thriving and I had several sightings during my visit. The best news of 2006 is that a pair of Nightjars Caprimulgus europaeus bred in the area for the first time since the late 1980s. White-spotted Pinion Cosmia diffinis (L.) The highly localised White-spotted Pinion moth Cosmia diffinis began flying, and possibly dispersing, early in 2006. On 22 July one was captured in perfect condition at Elton, Northamptonshire, the first record for the area (Brian Stone). Elms Ulmus spp., the larval foodplant, are well represented in the village, but Brian has not had the moth here before in several years of trapping and this result may represent a small extension of range. Monitoring of the known sites in Huntingdonshire and Cambridgeshire, by Ban'y Dickerson and others produced the moth in good numbers where sought. Ruth Edwards, who has the moth breeding on her farm in Cambridgeshire, considers 28 July to 6 August to be the time she captures most adults in her garden light-trap, although at other sites 10 August seems to be a good date to hit peak numbers. Unfortunately, the main stand of mature elms on her farm is suffering another wave of Dutch elm disease, and the majority of the trees had very thin canopies of leaves in 2006 and are clearly dying. Only three trees in the stand still had substantial leaf cover. I am helping Ruth to monitor the numbers of moths as the disease progresses, by placing traps in fixed positions nearer to the trees than Ruth is able. My light-trapping on 2 August 2006 confirmed the moth still present at both ends of the stand, but numbers appear to be dwindling. It will be exceptionally interesting and important in understanding the population dynamics of the moth in relation to the disease to continue recording after all the mature trees have died at this stand, which is likely in the next three years, and to see if the moth is able to survive on the lower regrowth alone or has to recolonise from elsewhere once the regrowth has grown larger. NOTES 131 On 2 August I discovered the White-spotted Pinion in a stand of tall elms nearly 100m in length at Longstanton, Cambridgeshire, as part of the BC Action for Threatened Moths Project (with thanks to Sharon Hearle and John Hobson). This is a site from which it has not been recorded before and where there are opportunities for planting additional, disease-resistant elms as part of a project to construction new housing in the area. It was a blustery cool night, poor for moths and one of a series of such nights at this time. By 22.15 hours I had a singleton of the species in an actinic trap within the elm stand in which only three moths of other species had been caught by this time. Running the trap until 23.00hrs produced no more and none came to a Robinson trap I was operating in the open by the elm trees. The moth was recorded in double figures on 9 August (by Mark Hammond et al.) at its known stronghold at Overhall Grove, Knapwell, which was discovered as a result of targeting the species for National Moth Night on 10 August 2001 (see Atropos 16: 34-37). On 11 August 2006, encouraged by Mark’s result, I investigated the four stands of English elms Ulmus procera at the RSPB estate at The Lodge, Sandy, Bedfordshire, with several new but keen moth recorders from the RSPB. Again it was blustery but the elms provided some shelter. We recorded one Lesser-spotted Pinion C. ajfinis but no White-spotted Pinion despite trapping all night. These stands of elms are within 2 km of the stand at Potton where, in 2005, John Day and I discovered the only currently known population in Bedfordshire (see BW 17: 54), and they are certainly worth surveying again on a calmer night. Silurian Eriopygodes imbecilla (Fabr.) (Red Data Book species, proposed UK BAP priority species) A break-through in our understanding of the larval ecology and phenology of the Silurian moth Eriopygodes imbecilla in the British Isles was made in April 2005 with the discovery of the first larvae to be found in the wild (see Ent. Rec. 118: 216- 217). However, the pre-hibernation phase of the life-cycle in the wild remained unknown, with no larvae having been found until the spring. Some progress on this subject was made on the afternoon of 22 September 2006 when Martin Anthoney and the author searched for and found a pre-hibernation caterpillar of the Silurian moth using a portable suction sampler at the site in the mountains of Monmouthshire where the moth was first discovered in Britain in 1972. This discovery clarifies the timing of the life-cycle and the stage and size at which this very rare species overwinters. We found the caterpillar at 18.02 hours in the ninth of a total of fifteen samples. Each sample involved one minute of “hoovering” in amongst the sward of Bilberry Vaccinium myrtillus, Heath Bedstraw Galium saxatile and fine grasses in which we had seen final instar caterpillars feeding on 13 April 2005, but had failed to find pre-hibernation larvae by sweep-netting on 1 September 2005 {Atropos 27: 20-23). The caterpillar measured 14mm in length and was found one and a half hours before dusk. After dark, Anthony Price and I suction-sampled a second site of similar high moorland habitat (500-600m above sea-level), 4 km to the north, where we have previously recorded both adult Silurian moths and post-hibernation larvae. Our first sample, at 21.20 hours, produced one Silurian larva and there were two 132 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 more in our third sample, but none in our last two of a total of five samples. All the larvae measured 13-14 mm in length when extended and active. Our previous work suggests the larvae are not more abundant at the second site. It is more likely that they are more easily sampled after dark because they are emerging from day-time hiding places amongst the vegetation. By day the captive larvae hid under leaves in the box in which they were placed, and when only one small Bilberry leaf was provided amongst grasses and Heath Bedstraw, all four larvae were found to have crammed themselves under this one. Although the larvae may have been wandering about after dark, a fifteen minute search by torch-light by Anthony and the author between 21.45-22.00 hours on this mild, calm night failed to reveal any larvae feeding, unlike similar searches in the spring, when larvae were found in prominent positions on Bilberry and Heath Bedstraw. The author thanks Martin Anthoney and Anthony Price for their help in the field, Mike Wilson of the National Museum of Wales, Cardiff, for the loan of two vacuum samplers, and the Monmouthshire Moth & Butterfly Group, the family of the late Neil Horton and the South Wales Branch of Butterfly Conservation for financial backing for this project. Scarce Hook-tip Sabra harpagula (Esper) (Red Data Book species but not a UK BAP priority species) On 28 June 2005 a female Scarce Hook-tip was captured, eggs obtained and larvae reared (see Ent. Rec. 118: 215-216 and BJENH 19: 254-257). The pupae were overwintered and in 2006 several adults emerged, from which a single fertile pairing was obtained on 6 June, and larvae subsequently reared as detailed for the previous year. The most noteworthy additional observation is that a single adult emerged outdoors on 16 November 2006 from a larva which had started off its development indoors, but which had been outdoors from the third instar. The summer of 2006 was markedly warmer than average, with prolonged intense heat in July in particular, and a very mild autumn. Clearly, the British population of the species is capable of producing a second generation, as it does routinely further south in Europe, but it would appear from the late date, in November, and that only one adult emerged, that the species is British population is strongly adapted not to do this. No fieldwork took place in 2006. The work in 2005 was assisted by a grant from the BENHS. Several of the studies undertaken form part of Butterfly Conservation’s Action for Threatened Moths Project, which is part funded by English Nature (now Natural England), and the author is indebted to nominated officers Mark Parsons (BC) and David Sheppard (EN) for helping to ensure continued funding. Other partners and colleagues are acknowledged within each section and I am most thankful to all of them. Private land-owners and some others are generally not named, for reasons of privacy and security, but their help is also greatly appreciated. — Paul Waring, Windmill View, 1366 Lincoln Road, Werrington, Peterborough, PE4 6LS (E-mail: paul_waring@btinternet.com). THE DOUBLE LINE 133 THE DOUBLE LINE MFra/MiVA TURCA (L.) (LEE: NOCTUIDAE): NOTES ON ITS HABITATS, FOODPLANTS AND SUGGESTED MANAGEMENT IN ENGLAND AND WALES WOLTON, R. J.', Spalding, A3 and Henwood, B. 'Locks Park Farm, Hatherleigh, Devon. EX20 3 LZ, ^ Tremayne Farm Cottage, Praze-an-Beeble, Camborne, Cornwall TR14 9PH, ^6, Lakeland, Abbotskerswell, Newton Abbot, Devon. TQ12 5YF Abstract The association of Mythimna turca (L.) (Lep.: Noctuidae) with open willow scrub, bracken scrub and Rhos pasture or Culm grasslands is discussed. Larval foodplants are listed, including previously unpublished data, and associations with the different vegetation communities are described. Management recommendations are provided, with the aim of creating or restoring tussocky swards (perhaps through light cattle grazing) closely interspersed with areas of short turf. Introduction The Double Line Mythimna turca (Linnaeus) is classed as Nationally Notable (occurring in less than one hundred 10km squares in Britain) and is a Priority Species within the UK Biodiversity Action Plan (UK Biodiversity Group, 1999). It is largely confined to Wales and south-west England, but is also known from a very few sites in south-east England (Waring & Townsend, 2003). It is listed in many moth identification guides as a woodland species (e.g. Porter, 1997, Skinner, 1998) and on some sites it appears to be associated with grassy woodland rides, e.g. in Wales (Fowles, 1988). Waring & Townsend (2003) list the following habitats: mature woodland, open oak woodland, wet rough acid grasslands. There are numerous records in Cornwall from woodland sites, e.g. Luckett in 1982 (Smith, 1997) and near Blisland in 1999 (Spalding, unpublished data). However, AS and RJW found Double Line in some numbers when surveying the Culm measure grasslands at Dunsdon in Devon (now a National Nature Reserve and a Devon Wildlife Trust reserve) (Spalding, 1989; Wolton, 2000) where the woodland areas were restricted to overgrown hedges between small open fields; as a consequence we decided that the moth may be more eclectic in its habitat requirements than formerly realised and may feed as larvae on plants growing on the woodland edge, perhaps taking advantage of the shelter provided. Subsequently, Double Line has been recorded on numerous Culm grassland sites in north and west Devon, often in considerable numbers. Indeed, in June it is sometimes the most numerous Noctuid caught in light traps, with up to 64 being caught in a single 15W actinic trap in one night. On Hollow Moor, a site in north-west Devon, 248 individuals were caught in six such traps on 1 July 2006 (RJW). It can be difficult to determine the exact habitat association of a moth species unless that species is sedentary. Double Line is a large moth which flies well and so its presence throughout an extensive site may disguise a particular association with 134 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 part of that site, for example the hedgerows within the Culm grassland habitat. This article outlines some of the work carried out to define habitat associations for Double Line using light traps and larval searches, with information on the larval foodplants, much of it previously unpublished. Habitats Double Line is known to occur in sites where some of the following habitats are present: • Woodland • dense woodland with rides and glades • open woodland • scrub • wet willow Salix spp. scrub • scattered gorse Ulex europaeus scrub • bracken Pteridium aquilinum scrub • Rhos pasture or Culm grasslands (species rich purple moor-grass Molinia caerulea or rush Juncus species pastures. At least some of these sites in south Wales and Cornwall are on abandoned mining areas (e.g. for coal or tin), where the sites have scrubbed over since industrial activity ceased. Between 2000 and 2002, three sites (Richmond Park in south London, Goss Moor National Nature Reserve in Cornwall and Margam Country Park in south Wales) where Double Line was known to occur were investigated using rows of light traps set in a line to sample different habitat types. The results were analysed on the basis that if Double Line has no habitat preferences, we would expect to catch the same number at each trap station. The results of these surveys are summarised in Spalding & Parsons (2004) and indicate that Double Line is often associated with the following habitats: • Open willow scrub with a rich grass flora (e.g., at Goss Moor) • Bracken scrub with abundant Common Bent Agrostis capillaris or Creeping Soft-grass Holcus mollis (e.g., at Richmond Park and Margam Country Park) • within woodland • open areas An additional light trap transect surveyed at St Clether (Spalding, unpublished data) suggested that bracken scrub within scattered European Gorse scrub was also an important habitat type. We have yet to run light trap transects within Culm grassland habitat. These findings confirmed our view that the Double Line is a species of woodland edge, open scrub and wet grassland, where both temperature and humidity may be THE DOUBLE LINE 135 higher than in more open areas. The association in some places with bracken is highlighted by the fact that the larvae are well camouflaged on dead bracken Pteridium aquilinum, being a similar colour and having dark lines which are reminiscent of the markings of a frond of dead bracken (Fig. 1). However, the larvae taken at Locks Park Farm in Devon did not have the cross-shaped dark dorsal markings described in Porter (1997) until just a day or two before pupation and all larvae are well camouflaged on dead oak leaves, dead grass etc. The larvae are not associated with bracken on Culm grassland sites. Double Line tends to be absent from dense woodland, even when known larval foodplants are present. For example, in Goss Moor no Double Line were recorded in dense shady willow woodland with a sparse ground flora which included the known larval foodplant Agrostis capillaris. Likewise, trapping well within a native broadleaved woodland during the flight peak season resulted in few Double Line being caught while they were numerous in adjacent Culm grassland in north-west Devon (RJW, unpublished). This result is despite the fact that we would expect the light trap to attract more moths in a dark woodland as the contrast between the lamp and the surrounding woodland is greater than in open areas, and the temperature is likely to be higher especially on windy nights; this factor was illustrated by the catch in a trap set in a small patch of lime Tilia sp. trees over a sparse ground layer at Margam Country Park which attracted large numbers of Double Line from adjacent bracken scrub; this woodland was darker than the surrounding grassland and also 2°C warmer at 11.30pm. The absence of Double Line from large stands of dense woodland may be due to the sparseness and lack of vigour of the ground flora, especially grasses and sedges, or perhaps due to the cooler cumulative temperatures. Double Line tend to be absent from open grassland well away from any trees or scrub, even where the foodplant grasses are abundant. Hence Double Line was largely absent from open deer-grazed grassland at Margam Country Park, with only three Double Line (out of 53 recorded on the site) being recorded despite the presence of the larval foodplant Holcus mollis. The results were even clearer for Richmond Park, where 105 Double Line were recorded in eight traps, yet none were recorded in the three traps set in open grassland (wet grassland with Molinea caerulea and acid grassland with Agrostis capillaris, both possible larval foodplants). This indicates that shelter (as provided by woodland, bracken or scattered scrub) is important for Double Line. Larvae Oviposition has been observed in Germany on the tip of a dead bushgrass Calamagrostis epigejos stalk that was bent at the top, the female inserting the strong ovipositor into the sheath surrounding the withered flower and depositing the eggs there (Steiner & Ebert, 1998). Larvae hatch in August and overwinter while small; there is then a period of active feeding at night in April and May before they pupate. The best time to find them is late April to early May when they are nearly full grown and are more easily seen. Typically they appear late in the evening, after 23.00 BST. 136 ENTOMOLOGIST'S RECORD, VOL. 119 25.V.2007 Larval foodplants are given in the literature as various grasses as well as wood- rush Luzula species Porter (1997), although Waring & Townsend (2003) suggest that the wood-rush records require confirmation. Grasses mentioned by various authors include Cock’s-foot Dactylis glomerata. Common Bent Agrostis capillaris. Creeping Soft-grass Holcus mollis and Wood Meadow-grass Poa nemomlis, but its Culm grassland habitat suggested that other foodplants may be utilised. In Germany the larvae are recorded as feeding on Carex brizoides (not found in Britain), Hairy Sedge Carex hirta and doubtfully Greater Stitchwort Stellaria holostea, in addition to various grasses (Steiner & Ebert, 1998). This article summarises the results of investigations by the three authors over several years, with unpublished information on the larval foodplants. Figure 1. Larva of Mythimna turca at rest on a dead frond of Bracken Pteridium aquilinum. Larval searches have been made at night between late March and early May at a variety of sites in Devon and Cornwall (Table 1). Larvae were found in smaller numbers than expected considering the large numbers of adults found at some of the sites, and it may be that many of the larvae are deep down in the grass and therefore difficult to find or perhaps that they do not feed every night. Larvae were recorded feeding on a wide range of foodplants (Table 1), including what we believe are the first records (by RJW and BPH) of feeding on Carnation Sedge Carex panicea. Glaucous Sedge Carex flacca, Purple Moor-grass Molinia THE DOUBLE LINE 137 caerulea. Sheep’s Fescue Festuca ovina and the bent grass Agrostis vinealis. The larvae can often be found resting on the ground (where they can be hard to see on the bare earth) or motionless on grass stems. They appear to be very slothful, and may remain in the same position for several hours without feeding. As a result, records of feeding activity have been difficult to obtain. In many cases, larvae were recorded resting on grass stems but not feeding; these positions were not considered as proof of feeding and only actual feeding records have been recorded. Larvae were recorded in five National Vegetation Classification (NVC) (Rodwell, 1998) grassland and mire communities often within willow woodland (Wl), European gorse scrub (W23) and bracken scrub (W25) - U4 and MGS (at Goss Moor & Breney Common), MGIO and M23 (Locks Park Farm) and M24c (Scadsbury Moor). At Goss Moor, despite extensive searching in early May 2000, no larvae were found in open grassland (a mix of Purple Moor-grass mire (NVC M25) and extensive rush pasture (NVC M23), even though one of the recorded foodplants Dactylis glome rata was present and several adults had been recorded here in July 1999. This area was grazed by cattle at low density. In Devon, at Scadsbury Moor, a few larvae were found up to 15m away from the field edge, but most were taken in a sheltered area near the woodland edge where the afternoon sun catches a south facing slope, creating a sheltered sun spot. At Goss Moor, larvae were taken on a narrow track running east- west and open to the sun during the day; at St Clether and Treslea Down in Cornwall larvae were found at the edge of bracken and gorse scrub on warm south-facing slopes. However, at Breney Common in Cornwall larvae were taken on the north side of willow scrub and within a willow woodland glade. Late instar larvae hide during the day. At Goss Moor on 10th May 2001, one larva was re-found in the morning concealed 5cm down in the moss layer below the grass stem on which it was feeding the previous night. At Scadsbury Moor, two larvae were re-found next morning, at about 10am, curled up on dead oak leaves under other leaves, with perhaps 7 cm of loose leaf letter above them, but not right on the cold, wet, ground (Fig. 2). It had been raining and the vegetation was wet, yet the larvae in their leaf shelters were dry. Neither tried to walk away when exposed to the light, and they were only a few cm away from the plants they had been eating. The larvae would doubtless get warm when the sun hit the location, perhaps helping their digestion. Feeding in captivity In captivity, RJW has recorded eggs being laid in batches of about 20 on false oat- grass Arrhenatherum elatius flower stalks c. L5mm in diameter so that they glued together two or three stems. The early instar larvae fed on the stems, leaves and flower heads of Agrostis stolonifera, apparently preferentially resting during the day on the dead leaves and flower heads of various grass species where they were well camouflaged. A wide range of grasses and sedges were taken by the larvae. Table 1. Feeding records of Mythimna turca larvae at sites in Devon and Cornwall 2000 - 2006 138 ENTOMOLOGIST’S RECORD, VOL. 119 25.V.2007 00 > -o s -O ^ S I P5' 0) bO 5 - § 60 s 5 i 00 ~s; .2 s 00 g .S ^ 2 ^ D- ^ S O I « oO O ra CO .2 « ll |.t B 3 «« s |i Q u S ^ ►2 'o ^ § ■§ I'i li^ o ;;2 ^ V I 5 .S X) .^1 § I' I s I ^ g a ^ li X) -o 3 (5) V-i .a x) « .5 S V o ^ •S ^ , -a S 8 ^ s g -3 s CJ ts S -3 ^ : S s S u 3 > .g I •-y r \ » U a -a cs S ^ -a § J U c/5 ^ XS K3 ^ 5- M ‘S 2 S I o J I S 8 X) ^ u > U (_ 60 ^ S -S '’B t:? (U > , « 3 BoM a “ 8 O t*-i l^S 2 D.W as-d III O § ^ 8 ^ « s ■S >> 8 I ^ s •“ Oc O § £ 53 .O S Q Ci, Cj o I ’I .^1 g ■at” ^1 « o g > S£ s.s '=* ^ ^ o 1 e 2 ^ ?S S3 S 4) II o Ofi'o 1 1 ^ .s 00 as if ta I ^ -I O - i © 4S §.^ Si b I I i P 8 £ S •^3 2^ S 8 g s o « Sis 2-§ I r ^ S CU >1,” z g 13 .3 O I •S “3 ^ ^ r? 3 S O O =« Q ? i 5^ S Cl, S ^ O O ^ •3 2 8 O 5pS ^'9 ^