Volume 49This newsletter is now available in electronic format. The preferred method of accessing the electronic version is through the World-Wide Web at the following Universal Resource Locator: http://www.ent.iastate.edu/fleanews/aboutfleanews.html or through either Gopher or anonymous FTP: gopher.ent.iastate.edu in the "Publications" directory. Electronic versions are available for No. 46, July, 1993; No. 47, December, 1993; No. 48, July, 1994 and this number.
The opinions and assertions contained herein are the private ones of the authors and are not to be construed as official or as reflecting the views of the Department of Entomology, Iowa State University or Sandoz Animal Health.
First, I wish to express my appreciation to all of you who responded to the announcement of the the death of Joanne with your condolences. It was most kind of you and I know that she would have appreciated the thoughts conveyed in your messages.
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In response to my review of the Lane and Crosskey book on Medical Insects and Arachnids (FN 47: 518-519), John Lane of the London School of Hygiene and Tropical Medicine, University of London wrote to remind me of two other volumes dealing with Medical and Veterinary Entomology. The first of these is Kettle, D.S., 1984, (reprinted with minor changes in 1990 and 1992), Medical and veterinary entomology. C*A*B International, Wallingford, Oxon, OX10 8DE, UK. 658 pp, ISBN 0-85198-701-X. The other, now out of print, is Service, M.W., 1980, A guide to medical entomology. The MacMillan Press Ltd., London. 226 pp. Both of these have evidently been used as texts, in conjunction with James and Harwood, 1979, in classes taught at the London School. My apologies for the omission.
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The following persons have sent literature since the publication of FN 48: A. Azad, J. Beaucournu, D. Cyprich, M. Dryden, A. Dudich, L. Durden, E. Easton, T. Galloway, K. Larsen, A. Olsen, R. Pilgrim, J. Segerman, P. Sleeman, P. Smiddy & M. Stanko. Thank you very much for your continued cooperation.
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A few new names have been added to the subscribers since Flea News 48. Their names and addresses follow.
Ms. Elvira Barchet, 6644 Clybourn Avenue, #76, North Hollywood, CA 91606
Dr. Gordon Gordh, Department of Entomology, University of Queensland, Brisbane, Queensland, AUSTRALIA
Prof. Andrew Main, Science Department, American University of Cairo, 113 Sharia Kasr el Aini, Cairo, EGYPT
Dr. Thomas Moore, Museum of Zoology, University of Michigan, Ann Arbor, MI 48109-1079
Dr. David R. Nash, Wohlenstrasse 50a , CH-3032 Hinterkappelen, SWITZERLAND
Mr. Dave Pehling, 600 128th Street SE, Everrett, WA 98208
Dr. Henry W. Robison, P.O.Box 1354 SAU, Southern Arkansas University, Magnolia, AR 71753-5000
Mr. Manfred Zimmermann, Baltzerstrasse 3, CH-3012 Bern, SWITZERLAND
Pat Zungoli, Box 340635, Cherry Farm Insectaries, Clemson University, Clemson, SC 29634-0365
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The Annual Report of the Danish Pest Infestation Laboratory (see Bille, N., 1994) lists the following studies on fleas conducted by Alice Olsen and Kim Søholt Larsen.
* 10.1 The cat flea Ctenocephalides felis. Four strains, two American and two Danish are in culture.
* 10.1.1 The pattern of emerging of the cat flea.
* 10.2 The squirrel flea Ceratophyllus [(Monopsyllus)] sciurorum sciurorum.
* 10.3 Laboratory and field evaluation of Dimilin for control of fleas on farmed mink. [C. (M.) s. sciurorum].
* 10.4 The hen flea Ceratophyllus [(Ceratophyllus)] gallinae.
* 10.5 Insecticidal effect of the plant Cassiope tetragone.
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"Many foreign countries have requirements for permits to take scientific specimens out of the country. The Lacey Act means it is now a U.S. federal crime to fail to comply with these permit rules - and ignorance is no excuse. A number of Fish and Wildlife Service enforcement agents in the lower 48 [states] have stated that the Lacey Act is retroactive in the following sense: if a museum has a 100-year old insect specimen that was originally (for example) taken from a foreign country without the requisite permit, that specimen is now in violation of the Lacey Act. Most major museums in the country have numerous specimens that have suddenly become contraband.
"All this is bad enough - but then the Fish and Wildlife Service got into the act by promulgating its own regulations. In order to bring scientific insect specimens into the U.S., or take them out of the U.S., the researcher now has to fill out F&WS Form 3-177. This form was originally designed for use by commercial importers of wildlife materials and products. It requires the importer /exporter to list every species of animal in the shipment, and the number of individuals of each species. Museum entomologists may return from a field trip with several thousand specimens, or even tens of thousands of specimens - and many, sometimes most, of these will probably be undetermined. You are allowed to bring in undetermined material - provided that you re-file Form 3-177 every 180 days until all the material has been determined to species! In many groups of insects it may take years, or even decades, to determine to species every specimen in even a small collection, so Form 3-177 amounts to a serious paperwork burden to any museum whose staff is actively working on foreign material. Failure to file the form makes you guilty of smuggling. Fortunately most F&WS enforcement agents will make exceptions to the Form 3-177 requirement in cases where the material cannot be enumerated (as for the millions of organisms present in soil samples). Travelers who have picked up diseases in foreign parts do not have to inventory their microorganisms...
"Other consequences of these F&WS regulations are: entomologists are being told that imported/exported specimens may not be sent through the mail, and that all imports and exports of specimens must take place through a limited number (nine) of official Ports of Entry. Packages of insect specimens are being opened and 'inspected' by people with no entomological training and no appreciation of how fragile such specimens are. Some foreign museums are considering refusing to lend material (especially type specimens) until the rules change.
"Recently proposed changes in the F&WS regulations would add a provision that importing eight or more similar specimens would create the presumption of commercial use! A reported conversation with the author of this provision indicated that eight beetles would be considered 'similar' regardless of how many species (or families) were involved.
"One of the major ways that the insect collection at the National Museum of Natural History grows is through donations of private collections. The NMNH has announced a new policy for donations: all specimens must be accompanied by copies of all relevant collecting permits or by written evidence that no such permits were required. The U.S. Department of Agriculture is requiring similar documentation on all specimens sent to them from foreign countries for determination.
"These laws and regulations are seriously impeding taxonomic and other work on insects and other 'lower' organisms, at the exact time that research on biodiversity is becoming of critical importance. The laws passed by well-meaning individuals, in a climate of opinion that has been affected by concern for the environment (and possibly by animal-rights groups) - with absolutely no understanding of the way insects and other lower organisms differ from vertebrates. Scientific collecting is no danger to insect populations! The fecundity of insects is so high that sheer destruction of habitat and competition from introduced species are the only factors of any importance for species survival.
"What should we do about this situation? The only hope for the future of entomological research is to get the Lacey Act, and the requirements for Form 3-177, changed so that for insects and other lower organism only threatened and endangered species are covered. The original Lacey Act even had a sentence beginning: "Nothing in this subsection shall restrict the importation of dead natural-history specimens for museums or for scientific collections ...", which seems to have been forgotten.
"Life on earth rests on lower organisms. We could vanish and life would go on - but if insects vanish we will all vanish with them. Research on insects needs to be untrammeled, for our own good. As far as biodiversity research goes, the current regulations amount to shooting oneself in the foot . . .
Kenelm W. Philip
Institute of Arctic Biology, University of Alaska, Fairbanks, AK
<fnkwp@aurora.alaska.edu>
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On an unrelated subject, Philip also sent the following description of a distribution map program that is now available.
Tundra Vole Software, 1590 North Becker Ridge Road, Fairbanks, AK 99709-2705
[907 479 2689]"
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Meanwhile, at least 12 cases have been reported in western United States. One of these in New Mexico resulted in a fatality. REL
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The following review of a new book by E. O. Wilson was recently published in the New Scientist (October 1st, p. 43) and is repeated here, with permission, both from the journal and the author.
"The indefatigable E. O. Wilson has recently published yet another work, and this one, an autobiography titled NATURALIST, is not being promoted much by Island Press, the small outfit that published it. It is a very good read throughout, but the long-suffering taxonomists, in particular, ought to enjoy his account of the attempt, during the 60s, by the molecular biologists to exterminate the ecologists and systematists. At Harvard the cast included Jim Watson himself, [to]whom Wilson is not kind. His account of departmental politics, with not just Watson and Wilson, but Ernst Mayr and George Wald, is amusing if you can stomach it. Near the end of the chapter, Wilson, looking back on it all, comments that 'molecular biologists, as they promised, have taken up evolutionary studies, making important contributions whenever they can find systematists to tell them the names of organisms'".
Jonathan D. Beard, 820 West End Avenue, 3B, New York City, NY 10025-5328, <jbeard@panix.com> - CIS 72301,563
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To those of you not directly concerned with the science of Entomology, the acronym IGR has probably been assigned to the dustbin of alphabetical nonsense so prevalent in American culture today. In fact, IGRs (=Insect Growth Regulators) have been around for some time, and in many instances represent the wave of the future in the control of certain insect pests. My first contact with one came in the days when I was still very much involved in raising orchids and found one of these compounds to be efficacious in controlling scale infestations and those of other homopterous insects. Today, at least one of these is used in controlling flea infestations in the home. Following is an excerpt from an article published in Pest Control Technology, February 22: 58, 62, 90 (1994) and reprinted in the Technical Information Bulletin of the Armed Forces Pest Management Board.
"IGRs work because they mimic the flea's own growth-regulating hormones, thus interfering with the flea's ability to complete its development. Whole generations of flea larvae are unable to hatch from their eggs, and larvae that hatch prior to the application will be unable to pupate and mature to adults. With the flea life cycle interrupted, the population crashes in a few weeks.
"In addition to reducing the amount of time spent controlling severe flea infestations, preventive IGR flea treatment programs offer several benefits stemming from the growth regulators themselves.
* "Because they closely resemble the flea's own hormones, IGRs aren't metabolized rapidly and fleas are less likely to evolve resistance to them.
* "Some IGRs are very photostable - they remain effective in sunny back yards.
* "Flea IGRs are available in a wide variety of formulations: emulsifiable concentrates, aerosols, wettable powders and IGR/adulticude sprays for direct application to pets (one has even been formulated specifically for puppies and kittens).
* "Flea IGRs remain active for 6-12 months after application.
* "IGRs provide a least-toxic chemical control alternative: even though IGRs have a long residual life, they are environmentally sound and safe for vertebrates when applied according to label instructions.
"Note that on occasion a flea may be brought into the home by a pet. Sighting a flea now and then shouldn't be taken as an indication of failure. IGRs won't relieve animals of all fleas, but they will prevent infestations in the home. Flea eggs that drop to the carpet will be affected since they or the larvae that hatch will never become a blood-feeding adult . . ."
[A similar level of euphoria was expressed by some with the development of chlorinated hydrocarbons, organophosphates, etc., now considered inefficaceous controls and major environmental pollutants. REL]
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The only remaining family, the Ceratophyllidae, was not included as a part of the catalogue series, but was the subject of the 1983 volume by R. Traub, M. Rothschild & J.F. Haddow. I have reason to believe that a limited number of copies of this volume may be available on a similar basis. Persons interested in obtaining a copy of this work should contact me personally and I will look into its availability. In addition to my mailing address, I may be contacted at any of the following: Tel. (515) 294 1815, (515) 232 7714, Fax. (515 294 5957) or E-mail <relewis@iastate.edu>. REL
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In keeping with the practice begun by Frans Smit in 1978 of assigning a 5-digit number to each name erected in the order, following are numbers assigned to those taxa described in 1992. Due to the difficulty in establishing the exact dates of publication the listing is alphabetical rather than chronological. Please inform me of any omissions that come to your attention.
99201 aethiopica Beaucournu & Morel, Chiastopsylla. Ann. Soc. Ent. Fr. (N.S.) 28(2): 125-131.
99202 caecus Beaucournu & Morel, Ctenophthalmus (Ethioctenophthalmus). Ann. Soc. Ent. Fr. (N.S.) 28(2): 125-131.
99203 iae Beaucournu & Kock, Nycteridopsylla. Senckenberg. Biol. 72(4/6): 329-334.
99204 laxiprojectus LI, Ctenophthalmus (Sinoctenophthalmus). In "The Anoplura and Siphonaptera of Guizhou" pp. 269-271.
99205 lushuiensis GONG & HUANG, Ctenophthalmus (Sinoctenophthalmus). Acta Ent. Sin. 35(1): 110-112.
99206 nushanensis GONG & LI, Palaeopsylla. Acta Zootax. Sin. 17(2): 235-237.
99207 parthicus Medvedev & Alifirenko, Ctenophthalmus (Euctenophthalmus). Parazitologiya 26(5: 409-417.
99208 quadrata GONG, Geusibia. Acta Zootax. Sin. 17(3): 363-365.
99209 scalonae Kotti, Frontopsylla (Frontopsylla). Zool. Zh. 71(11): 152-154.
99210 weiningensis LI, Amphipsylla. In "The Anoplura and Siphonaptera of Guizhou" pp. 314-316.
99211 xiei GONG & DUAN, Ctenophthalmus (Sinoctenophthalmus). Acta Zootax. Sin. 17(1): 97-99.
99212 zii GONG, Hystrichopsylla. Acta Ent. Sin. 35(2): 241-243.
Additional Taxa
1993
Leptopsylla algira atlantidis Beau cournu
Ctenophthalmus (Sinoctenophthal mus) exiensis WANG & LIU
Hechtiella lopesi Guimaraes & Lin ardi
Neopsylla siboi YE & YU
Chaetopsylla zhengi XIE, HE & CHAO
1994
Echidnophaga iberica Ribeiro, Luci entes, Osacar & Calvete *n.b.
Lagaropsylla malayana Beaucournu & Kock
Thrassis peninsularis Lewis
[*n.b. There is absolutely no excuse for attributing a new name to more than a maximum of two authors, and editors should be encouraged to refuse multiple-authored descriptions.]
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Although it may not be obvious from the titles, citations included here pertain to fleas and the zoonoses associated with them. Additional information is available upon request.
1988 (List 12)
CAO Li-ping & HE Lin. Comparative analysis of isoenzymes from three species of fleas. Annual Bulletin of the Society of Parasitology, Guang-dong Province 10: 219-220.
CAO Li-ping & HE Lin. Cytogenetic studies on fleas (Siphonaptera). IV. Comparative analysis of amino acids, DNA contents of three species of fleas. Annual Bulletin of the Society of Parasitology, Guangdong Province 10: 221-222.
CAO Li-ping & HE Lin. Cytogenetic studies on fleas (Siphonaptera). I. Technique of chromosome, DNA content, amino acids and isoenzymes of fleas. Annual Bulletin of the Society of Parasitology, Guangdong Province 10: 223-224.
1990 (List 9)
Trotti, G.C., L. Corradini & S. Visconti. Indagine parassitologica in un rifugio per gatti a Ferrara. Parassitologiia 32: 42-43.
1991 (List 8)
Dudich, A. To the knowledge of the fauna of fleas (Siphonaptera) living on small mammals in Oravské Beskydy Mts. Prehl'ad odbornych vysledkov XXVII. TOP - Oravská priehrada, 1991. pp 55-60. (in Czech)
Joseph, S.A. & G. Karunamoorthy. Studies on the haematophagous arthropods of zoonotic importance in Tamil Nadu. In Entomology for Defence Services. Proceedings of the Symposium held on 12-14 September. [edited by P.K. Ramachandran, D. Sukumaran & S.S. Rao]. pp. 185-192.
PAN Xiao-jun. A study of the phallosome of two male fleas of the family Pygiopsyllidae. Annual Bulletin of the Society of Parasitology, Guangdong Province 11-13: 109.
1992 (List 6)
Carabeli, A., R. di Vincenzo, P. Vanotti & E. Bertani. La Tungose. Nouvelles Dermatologiques 11(10): 826.
Dudich, A. Qualitative structure of the synusia of ectoparasites on small mammals in the supramontane belt of the west Tatra. Zborník Prác o Tatranskom Národnom Parku, 1992. 32: 149-164. (in Czech)
Dudich, A. Introgressive hybridization of subspecies of Ctenophthalmus agyrtes (Heller, 1986) [sic!]) (Siphonaptera, Ctenophthalmidae) in the Donau lowland. Spravodaj Podunajského Múzea Komárne Prírodné vedy 10: 172-185. (in Czech)
Dudich, A. Contribution to the knowledge of the small mammals (Insectivora, Rodentia) and their ectoparasites (Acarina, Anoplura, Siphonaptera) in the forest-steppe of the Cenkov State Nature Reserve (Donau lowlands). Spravodaj Podunajského Múzea Komárne Prírodné vedy 10: 186-191. (in Czech)
Pegram, R.G & A.J. Higgins. Camel ectoparasites: a review. In Proceedings of the First International Camel Conference, Dubai, 2nd-6th February 1992. [edited by W.R. Allen, A.J. Higgins, I.G. Mayhew, D.H. Snow & J.F. Wade]. pp. 69-78.
Slodobyanyuk, O.V. Taxonomic significance of morphological characters of insect-parasitic females of Tylenchida. Trudy Gel'mintologicheskoi Laboratorii 39: 171-179.
Smiddy, P. & D.P. Sleeman. Records of the flea Dasypsyllus gallinulae gallinulae (Dale) from nests of Irish dippers (Cinclus cinclus hibernicus Hartert). Irish Naturalist's Journal 24(4): 169-170.
1993 (List 4)
Bandyopadhyay, B. & J.S. Sarma. Therapeutic evaluation of deltamethrin and amitraz against organophosphate resistant canine ticks and fleas. Indian Veterinary Journal 70(11): 1053-1054.
Beaucournu, J.C. Leptopsylla algira atlantidis n. ssp. (Insecta, Siphonaptera), endemique des iles Canaries. Bulletin de la Société Française Parasitologie 11(2): 259-263.
Beaucournu, J.C. & J.A. Alcover. XXV. Els Sifonàpters. In J.A. Alcover, E. Ballesteros & J.J. Fornós (Eds.), Història Natural de l'Arxipèlag de Cabrera, CSIC-Edit. Moll. Mon. Soc. Hist. Nat. Balears 2: 377-382.
Beaucournu, J.C., C. Guiguen & B. Ehanno. Les Siphonaptères du massif armoricain et su sudouest des isles Britanniques comparison a partir de quelgues groupes - hôtes. Bulletin de la Société Scientifique, Bretagne 64(1): 209-222.
Beaucournu, J.C., M. le Piver & C. Guiguen. Acualité de la conquête de l'Afrique intertropical par Pulex irritans Linné, 1758. Bulletin de la Société de Pathologie Exotique 86: 290-294.
Campbell, J., J. Lowe, S. Walz & J. Ezzell. Rapid and specific identification of Yersinia pestis by using a nested polymerase chain reaction procedure. Journal of Clinical Microbiology 31(3): 758-759.
Degeilh, B., B. Gilot, C. Guiguen & J.C. Beaucournu. A propos de recoltes des puces (Siphonaptera) au drapeau. Bulletin de la Société Française Parasitologie 11(2): 253-258.
Dudich, A. The siphonaptorological bibliography of Slovakia. II. (1984-1986). Správy Slovenskej Zoologickej Spolocnosti, 1993. 15: 29-40. (in Czech)
Dudich, A. To the knowledge of micromammals and their ectoparasites in Ponitrie region. 1. Teriologic and parasitologic bibliography of Nitra district. Rosalia (Nitra) 9: 189-208. (in Czech)
Dudich, A. To the knowledge of micromammals and their ectoparasites in Ponitrie region. 3. Fleas /Siphonaptera/ of mammals /Mammalia/ living in Nitra district. Rosalia (Nitra) 9: 241-272. (in Czech)
Dudich, A. Fleas (Siphonaptera) of small mammals (Insectivora, Chiroptera & Rodentia) in the Bükk National Park. In The fauna of the Bükk National Park, 1993. pp. 401-406.
El-Bahrawy, A.A. & M.A. Al-Dakhil. Studies on the ectoparasites (fleas and lice) on rodents in Riyahd and its surroundings, Saudi Arabia. Journal of the Egyptian Society of Parasitology 23(3): 723-735.
Fain, A. & J.C. Beaucournu. Les hypopes des Astigmates (Acari) phorétiques sur les Puces (Siphonaptera) de Mammiféres et d'Oiseaux. Bulletin de la Institut Royal des Sciences Naturelles de Belgique. Entomology 63: 77-93.
Fukase, T. & M. Hosaka. Parasite life cycle diagrams. Ctenocephalides canis and Ctenocephalides felis. Journal of Veterinary Medicine, Japan 46(6): 500.
Guiguen, C., P. Yésou & J.C. Beaucournu. Notes sur Ceratophyllus vagabundus vagabundus (Boheman), 1865, au Lac Baikal (Siphonaptera: Ceratophyllidae). Bulletin de la Société Entomologique de France 98(1): 28.
Hayasaki, M., Y. Akiyama, K. Konno & I. Ohishi. Immune treatment of flea allergy dermatitis of dogs with flea extract. Journal of the Japanese Veterinary Medical Association 46(10): 866-869.
Heath, A.W., A. Arfsten, M. Yamanaka, M. Dryden & B. Dale. Vaccination against the cat flea, Ctenocephalides felis felis. Parasite Immunology 16(4): 187-199.
Hickey, G.J., C.H. Chang, F. Marsilio, W. Trimboli & E.L. Rickes. Effects of prednisone on dermal responses in flea-allergen hypersensitized dogs. Veterinary Dermatology 4(2): 71-77.
Hinnebusch, J. & T.H. Schwan. New method for plague surveillance using polymerase chain reaction to detect Yersinea pestis in fleas. Journal of Clinical Microbiology 31(6): 1511-1514.
Kocianová, E., O. Kozuch, P. Bakoss, J. Rehácek & E. Kovácová. The prevalence of small terrestrial mammals infected with tick-borne encephalitis virus and leptospirae in the foothills of the southern Bavarian forest, Germany. Applied Parasitology 34(4): 283-290.
Matskási, I. István Szabó is 80 years old. Parasitologia Hungarica 26: 59-66. (in Hungarian)
Mbuthia, P.G., T.A. Ngatia & J.P.O. Wamukoya. Occurrence of bovine skin diseases in Kenya. Bulletin of Animal Health and Production in Africa 41(4): 311-316.
Mir, A.S., B.A. Pandit, R.A. Shahardar & M.A.A. Banday. Prevalence of ectoparasites in indigenous fowls of the Kashmir Valley. Indian Veterinary Journal 70(11): 1071-1072.
Mumcuoglu, K.Y., J. Miller, O. Manor, F. Ben-Yshai & S. Klaus. The prevalence of ectoparasites in Ethiopian immigrants. In The Ethiopian immigrations to Israel - medical, epidemiological and health aspects. [edited by A.J. Rubinstein]. Israel Journal of Medical Sciences 29(6/7): 371-373.
Prelaud, P. Controle de l'infestation par les puces dans l'environment. Action Vétérinaire 1247: 7 ... 12.
Raue, H. Nytt behandlingsalternativ vid lopproblem hos hund och katt. [A new treatment for the flea problem in cats and dogs.] Svensk Veterinärtidning 45(11): 485-487.
Saari, R. Koiraheisimato (Dipylidium caninum) - tuontikoirien tuliainen. [Dipylidium caninum - in imported dogs.] Suomen Eläinlääkärilehti 99(12): 749-753.
Shoukry, A., G.A. El-Kady, T.A. Morsy & M.M.I. Salama. Rodents and their arthropod ectoparasites in South Sinai Governorate, Egypt. Journal of the Egyptian Society of Parasitology 23(3): 775-783.
Smiddy P. & D.P. Sleeman. Avian fleas in Ireland: a review of their distribution and hosts. Irish Birds 5: 55-60.
Stork, N.E. & C.H.C. Lyal. Extinction or 'coextinction' rates? Nature 366: 307 (25 November).
Watanabe, T., Y. Horii & Y. Nawa. A case of Dipylidium caninum infection in an infant - the first case found in Miyaaki Prefecture, Japan. Japanese Journal of Parasitology 42(3): 234-236.
Zuchowska, E. Choroby inwazyjne jezy. [Parasitoses and ectoparasites in hedgehogs.] Magazyn Weternaryjny 2(4): 35-36.
1994 (List 2)
Ambros, M., A. Dudich & J. Kovácik. A survey of ectoparasites and nidicolous arthropods of small mammals of the Mt. Babia hora (Oravske Beskydy Mts). Zborník Oravského Múzea, 1994. 11: 12-15. (in Czech)
Arellano, E. & D.S. Rogers. Reithrodontomys tenuirostris. Mammalian Species 477: 1-3.
Awumbila B. & E. Bokuma. Survey of pesticides used in the control of ectoparasites of farm animals in Ghana. Tropical Animal Health and Production 26(1): 7-12.
Beaucournu, J.C. & D. Kock. The genus Lagaropsylla Jordan & Rothschild, 1921 (Siphonaptera: Ischnopsyllidae). Annales de la Société de Entomologique du France 30(2): 193-108.
Beaucournu, J.C. & D. Kock. Notes sur les Ischnopsyllidae de la Région Orientale. II. Stations inédites et description d'une espèce nouvelle du genere Lagaropsylla Jordan & Rothschild, 1921 (Insecta: Siphonaptera). Senckenbergiana Biologia 73(1-2): 67-75.
Best, T.L. Chaetodipus nelsoni. Mammalian Species 484: 1-6.
Best, T.L., R.G. Clawson & J.A. Clawson. Tamias speciosus. Mammalian Species. 478: 1-9.
Best, T. L. & N.J. Granai. Tamias obscurus. Mammalian Species 472: 1-6.
Best, T. L. & N.J. Granai. Tamias merriami. Mammalian Species 476: 1-9.
Best, T. L. & M.P. Skupski. Perognathus flavus. Mammalian Species 471: 1-10.
Best, T. L. & M.P. Skupski. Perognathus merriami Mammalian Species 473: 1-7.
Bille, N., (Ed.). Danish Pest Infestation Laboratory Annual Report, 1993. 76 pp.
Billingsley, P.F. Vector-Parasite interactions for vaccine development. International Journal of Parasitology 24(1): 53-58.
Bogdanowicz, W. Myotis daubentoni. Mammalian Species 475: 1-9.
Buck, W.B. [& M. Dryden & J.S. Greek]. Correspondence. (Questioning the safety of an in-home flea product.) Veterinary Medicine 89(1): 935-941.
Carraway, L.N. & B.J. Verts. Sciurus griseus. Mammalian Species 474: 1-7.
Cyprich, D. & A. Dudich. Ectoparasites of small mammals (Insectivora, Rodentia) of Mt. Babia hora in Stredne Beskydy Mts (Western Carpathians). Zborník Oravského Múzea, 1994. 11: 7-10. (in Czech)
Dryden, M.W., J.E. Boyer & V. Smith. Techniques for estimating on-animal populations of Ctenocephalides felis (Siphonaptera: Pulicidae). Journal of Medical Entomology 31(4): 631-634.
Dudich, A. Flea subspecies new for the Slovakian fauna. Biologia 49(2): 238.
Eiseman, C.H. & K.C. Binnington. The peritrophic membrane: its formation, structure, chemical composition and permeability in relation to vaccination against ectoparasitic arthropods. International Journal of Parasitology 24(1): 15-26.
Elvin, C.M. & D.H. Kemp. Generic approaches to obtaining efficacious antigens from vector arthropods. International Journal of Parasitology 24(1): 67-82.
Fisher, M.A., M.A. Hutchinson, M.J. Hutchinson, D.E. Jacobs & I.G.C. Dick. Comparative efficacy of Fenthion, Dichlorvos Fenitrothion and Permethrin against the flea Ctenocephalides felis on the dog. Journal of Small Animal Practice 35(5): 244-247.
Greek, J.S. Environmental flea control - general guidelines and recent advances. Veterinary Medicine 89(8): 763-769.
Heckenberg, K., S.D. Costa, L.M. Gregory, B.F. Endris & W.L. Shoop. Comparison of thumb-counting and comb-counting methods to determine Ctenocephalides felis infestation levels on dogs. Veterinary Parasitology 53(1/2): 153-157.
Henry, C.S. Singing and cryptic speciation in insects. Trees 9(10): 388-392.
Higgins, J.A., J.B. Sacci, Jr., M.E. Schriefer, R.G. Endris & A.F. Azad. Molecular identification of rickettsialike microorganisms associated with colonized cat fleas (Ctenocephalides felis). Insect Molecular Biology 3(1): 27-33.
Hink, W.F., M. Zakson & S. Barnett. Evaluation of a single oral dose of Lufenuron to control flea infestations in dogs. American Journal of Veterinary Research 55(6): 822-824.
Koprowski, J.L. Sciurus carolinensis. Mammalian Species 480: 1-9.
Koprowski, J.L. Sciurus niger. Mammalian Species 479: 1-9.
Lehane, M. J. Digestive enzymes, haemolysins and symbionts in the search for vaccines against bloodsucking insects. International Journal of Parasitology 24(1): 27-32.
Lewis, R.E. A new species of Thrassis from Baja California, Mexico (Siphonaptera: Ceratophyllidae: Oropsyllinae). Journal of the New York Entomological Society 101(4): 536-541.
Lewis, R.E. & J.H. Lewis. Siphonaptera of North America north of Mexico: Hystrichopsyllidae s. str. Journal of Medical Entomology 31(6): 795-812.
Linardi, P.M., A.F. Gomes, J.R. Botelho & C.M. Lisboa-Lopes. Some ectoparasites of commensal rodents from Huambo, Angola. Journal of Medical Entomology 31(5): 754-756.
Linley, J.R., A.H. Benton & J.F. Day. Ultrastructure of the eggs of seven flea species (Siphonaptera). Journal of Medical Entomology 31(6): 813-827.
Maihuay, C., V. Pacheco & S. Solari. Siphonaptera (Insecta) en roedores silvestres del Cusco. Revista Peruana de Entomologia 36: 27-28.
Mappes, T., J. Mappes & J. Kotiaho. Ectoparasites, nest site choice and breeding success in the pied flycatcher. Oecologia 98(2): 147-149.
Medleau, L. Up-to-date aids in the fight against fleas and other ectoparasites - introduction. Veterinary Medicine 89(8): 762.
Moller, A.P., F. de Lope, J. Moreno, G. Gonzales & J.J. Parez. Ectoparasites and host energetics: house martin bugs and house martin nestlings. Oecologia 98(3-4): 263-268.
Nolan, K. Flea collars may cause erratic behaviour. Irish Veterinary Journal 47(5): 230.
Pung, O.J., L.A. Durden, C.W. Banks & D.N. Jones. Ectoparasites of opossums and raccoons in southeastern Georgia. Journal of Medical Entomology 31(6): 915-919.
Raschka, C., R. Ribbeck & W. Haupt. Untersuchungen zum Ektoparasiten-befall bei streunenden Katzen. Monatschefte für Veterinärmedizin 49(6): 257-261.
Ribeiro, H., J. Lucientes, J.J. Osacar & C. Calvete. A new species of flea (Siphonaptera: Pulicidae) from Spain. Journal of Medical Entomology 31(6): 887-889.
Roosje, P.J. Tiguvon Spot on for flea control. Tijdschrifte voor Diergeneeskunde 119(7): 219.
Sauer, J.R., J.L. McSwain & R.C. Essenberg. Cell membrane receptors and regulation of cell function in ticks and bloodsucking insects. International Journal of Parasitology 24(1): 33-52.
Schriefer, M.E., J.B. Sacci, Jr., J.P. Taylor, J.A. Higgins & A.F. Azad. Murine typhus: updated roles of multiple urban components and a second typhus-like rickettsia. Journal of Medical Entomology 31(5): 681-685.
Sleeman, D.P. & P. Smiddy. Bat fleas in Ireland: a review. Irish Naturalist's Journal 24(11): 444-448.
Sleeman, D.P. & P. Smiddy. Records of fleas (Siphonaptera) from Irish mammals and birds. Irish Naturalist's Journal 24(11): 465-467.
Staaden, M.J. van. Suricata suricatta. Mammalian Species 483: 1-8.
Stanko, M. Fleas synusy (Siphonaptera) of small mammals from the central part of the East-Slovakia lowlands. Biologia, Bratislava 49(2): 239-246.
Stolper, R. & J.P. Opdebeeck. Flea allergy dermatitis in dogs diagnosed by intradermal skin tests. Research in Veterinary Science 57(1): 21-27.
Stone, B.F., M.A. Shipstone, K.V. Mason, M. Cunningham & C.W. Wong. Efficacy of Permethrin in controlling the Australian paralysis tick Ixodes holocyclus and the cat flea Ctenocephalides felis on dogs. Australian Veterinary Journal 71(3): 90-91.
Trpis, M. Host-parasite relationships between fleas (Siphonaptera) and bats (Chiroptera) hibernating in ice and limestone caves in Slovakia. Bulletin of the Society for Vector Ecology 19(1): 8-12.
Trpis, M. Host-parasite relationships between fleas (Siphonaptera) and small mammals in the Tatras Mountains of Slovakia. Bulletin of the Society for Vector Ecology 19(1): 13-17.
Trpis, M. Host specificity and ecology of fleas (Siphonaptera) of small mammals in mountains of north-central Slovakia. Bulletin of the Society for Vector Ecology 19(1): 18-22.
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In an interesting letter to the British Journal NATURE (366: 307, 25 November) Nigel Stork and Christopher Lyal discuss the extinction of endo- and ectoparasites, along with the extinction of their hosts. The authors suggest that in at least one group of insects, the lice (Phthiraptera) and possibly another, fleas (Siphonaptera), the extinction rates approximate those of their avian and mammalian hosts. This is particularly the case in the lice because of their high degree of host specificity. Using the passenger pigeon and its extinction in 1914 as an example, they note that at least two species of chewing lice, Columbicola extinctus Malcomson and Campanulotes defectus Tendeiro, evidently became extinct at the same time as their host, relatively unnoted by the scientific community. They go on to point out that most people "consider the value of insects, either positive or negative (with perhaps the exception of butterflies), solely in terms of their contribution to ecosystems and their direct or indirect effect on humans." Whether its lice should be given the same value as their avian host raises ethical questions that should not be ignored when discussing conservation priorities and practices. If conservation needs require the extinction of their parasites while conserving the host species, such practices should be pursued ". . . in the full knowledge of what is being lost."
This has long been a matter of lively discussion among pulicologists since many families of fleas show phylogenetic affinities within the order that suggest extinction patterns of certain of their mammalian hosts. It is seldom noted that while hemimetabolous parasites such as lice pass all of their life stages on the host, the holometabolous fleas differ drastically in their requirements between the larvae and the adults and the law of the minimum applies to both stages. While we can never accurately reconstruct the phylogenetic position of these extinct taxa in a current context, a hypothetical example taken from the North American fauna demonstrates the potential damage to our studies created by host extinctions.
The host is the mountain beaver, Aplodontia rufa, a primitive rodent with a restricted range from northern Califonia to extreme southwestern British Columbia. According to the literature, ten species of fleas have been reported from this host. Five of these are obviously strays from other hosts, or at least accidental associations. Another, while found on this and other rodent hosts fairly frequently, is mainly a parasite of insectivores (shrews and moles). The remaining four are specific parasites of A. rufa and are almost never found on other hosts. Four genera are represented and three of these are monotypic. Depending on the family classification followed, either two or three separate families are represented.
The first of these is Dolichopsyllus stylosus (Baker, 1904) (Leptopsyllidae, Amphipsyllinae, Dolichopsyllini). The proper phylogenetic position of this taxon is very much a matter of speculation. According to current family definition it is a leptopsyllid but it is not in the mainstream of evolution in the family. That it is larger and hairier than other members of the family suggests its primitivity. However, the presence of a well developed pronotal ctenidium and the loss of eyes suggest some specialization as a parasite of a semifossorial host. In my view, its extincton would eliminate what I consider to be the most plesiomorphic member of the entire family.
The remaining three species are hystrichopsylloids, usually considered to be the most primitive superfamily in the order. The first of these, Hystrichopsylla schefferi Chapin, 1919 (Hystrichopsyllidae, Hystrichopsyllinae, Hystrichopsyllini), is a member of an Holarctic genus containing 19 species and 32 named taxa. Only seven species occur in the Nearctic Region, and all except H. schefferi are associated with rodent and insectivore hosts. Hystrichopsylla schefferi has the distinction of being the largest, non-neosomic flea in the entire order, and females may exceed one centimeter in length. All members of the genus are considered primitive by most students of the order and the most plesiomorphic taxa seem mostly associated with insectivores, although host specificity is not particularly strong in this genus. That the largest and one of the most primitive species is associated with such a primitive host suggests a fascinating evolutionary complex of taxa that has been lost to us through extinction of their hosts. Lewis & Lewis (1994) discuss this species in more detail.
Both of the other two taxa are monotypic and both are assigned to the family Ctenophthalmidae, Rhadinopsyllinae, Rhadinopsyllini. The eighty odd taxa assigned to this tribe are all nest fleas in that they have lost the ability to jump well and are confined to the nest of the host during most or all of their existance, both as larvae and adults. Members of the Palaearctic genus Stenischia are shrew fleas, while species of the Holarctic Rhadinopsylla parasitize rodents and/or insectivores, depending upon the subgenus to which they belong. Paratyphloceras oregonensis Ewing, 1940 and Trichopsylloides oregonensis Ewing, 1938, are exclusively parasites of A. rufa and are seldom taken on any other host species. It is apparent that Stenischia and Rhadinopsylla are closely related, in spite of the strong tergal and sternal incrassations of the abdomen in the former genus, and Stenischia rhadinopsylloides Smit, 1975, connects the two genera quite obviously. While both of the Aplodontia parasites are distinct from this line of evolution in the tribe, they are both much more setose, and P. oregonensis is much larger than any other member of the tribe. The genal ctenidium is present in this species, which is normal in the tribe, but it is missing or vestigial in T. oregonensis. All males in this tribe normally lack antepygidial bristles, an apomorphic character in the order, but a pair of these bristles is present in males of P. oregonensis.
In summary, while neither of these fleas seem to be in the mainstream of evolution within the tribe, each shows traits that are thought to be ancestral. Consequently, their loss could severely dampen phylogenetic studies in this large and important family of fleas. As pointed out by Lewis and Lewis (1994) these strongly host-specific species may become the first fleas to be placed on the Endangered Species list since at least two subspecies of A. rufa are seriously threatened by habitat reduction due to housing developments and other types of construction. REL
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We wish you the happiest of holiday seasons and the best of New Years!