Fish Meal as a Food for Clothes Moths

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Experiments have demonstrated that fish meal is a food highly satisfactory to larvae of the webbing clothes moth. Insects reared on this material went through their life cycles in a surprisingly short time. With fish meal as the only food supply, a method has been developed for rearing large numbers of clothes moths in gallon sized cardboard cartons.

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  • Research Article
  • Cite Count Icon 63
  • 10.1017/s0007485300046708
The Larvae of the Species of Tineidae of Economic Importance
  • Jul 1, 1956
  • Bulletin of Entomological Research
  • H E Hinton

Keys are provided for the larvae of 32 species of TINEIDAE, and detailed descriptions are given of 31 species. These include most of the species known to be of any economic importance. What is known of the biology of each is briefly summarised, but no attempt has been made to collate the available information on control measures.No larvae have been available of four species of some economic importance nor of twelve others of doubtful status as pests. The literature on each of these species is noted.The larvae of a few species of no known economic importance are described and are included in the keys. Most of these are very closely related to species known to be pests.The keys and descriptions include 21 species which are indigenous to Britain or are established here, so that keys and descriptions are now provided for half of the British species ofTineidae.

  • Research Article
  • Cite Count Icon 13
  • 10.1086/394510
Aberrant Feeding Behavior Among Insects and Its Bearing on the Development of Specialized Food Habits
  • Sep 1, 1936
  • The Quarterly Review of Biology
  • Charles T Brues

ABERRANT FEEDING BEHAVIOR AMONG INSECTS AND ITS BEARING ON THE DEVELOPMENT OF SPECIALIZED FOOD HABITS BY CHARLES T. BRUES Harvard University T HE behavior of insects with relation to food is extremely diverse if we consider them as a group. Any survey of its component parts reveals at once a more or less orderly distribution of the several types of food-habits with reference to characteristic peculiarities of structure, development and instinct. The dependence of trophic behavior upon the adjustment of such intrinsic factors to the environment is obvious, and we must look for any indications of the origin and development of predatism, vegetarianism, parasitism and the like by inquiry into the interactions of these internal and external modifications. Diversity in behavior among insects is readily traceable to their extremely plastic structural organization which admits of many drastic changes in the form of bodily parts, such as the mouthparts, legs, respiratory system, wings, etc. Such structural peculiarities frequently appear without associated modifications in other structures and correspond almost invariably to changes in habits to which they are highly, often exquisitely adapted. Whatever theoretical interpretation we may apply to the origin of these adaptations, their occurrence is real and by no means infrequent. Many cases of peculiar food-relations appear to be primarily of this nature. The indirect development of the higher insects opens new avenues for the initiation of profound although transitory structural modifications in the nymphal and larval stages, since the latter are interpolated in such a way that they may develop at this time entirely novel characteristics which leave no impress upon the imago.

  • Research Article
  • Cite Count Icon 24
  • 10.1086/physzool.10.3.30151419
Nutritional Studies of the Webbing Clothes Moth Tineola bisselliella Hum
  • Jul 1, 1937
  • Physiological Zoology
  • Mary F Crowell + 1 more

Previous article No AccessNutritional Studies of the Webbing Clothes Moth Tineola bisselliella HumMary F. Crowell and C. M. McCayMary F. Crowell Search for more articles by this author and C. M. McCay Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by Volume 10, Number 3Jul., 1937 Article DOIhttps://doi.org/10.1086/physzool.10.3.30151419 Views: 5Total views on this site Citations: 20Citations are reported from Crossref Journal History This article was published in Physiological Zoology (1928-1998), which is continued by Physiological and Biochemical Zoology (1999-present). PDF download Crossref reports the following articles citing this article:Kiyoshiro Goto, Sadahisa Yagi, Johei Oku, Shunsuke Tomura, Daisuke Yamaguchi, Toshiya Hirowatari Surveys on detritivorous moths using bait traps in Japan, Journal of Asia-Pacific Biodiversity 14, no.33 (Sep 2021): 386–398.https://doi.org/10.1016/j.japb.2021.03.011Steven J. McNeil, Matthew R. Sunderland The nanocidal and antifeedant activities of titanium dioxide desiccant toward wool-digesting Tineola bisselliella moth larvae, Clean Technologies and Environmental Policy 18, no.33 (Oct 2015): 843–852.https://doi.org/10.1007/s10098-015-1060-4Pascal Querner Linking webbing clothes moths to infested objects or other food sources in museums, Studies in Conservation 61, no.sup1sup1 (Apr 2016): 111–117.https://doi.org/10.1179/2047058414Y.0000000153P.D. Cox, D.B. Pinniger Biology, behaviour and environmentally sustainable control of Tineola bisselliella (Hummel) (Lepidoptera: Tineidae), Journal of Stored Products Research 43, no.11 (Jan 2007): 2–32.https://doi.org/10.1016/j.jspr.2005.08.004R. Plarre, K. Lieber, W. Burkholder, J. Phillips Host and host instar preference of Apanteles carpatus (Say) (Hymenoptera: Braconidae) a possible parasitoid for biological control of clothes moths (Lepidoptera: Tineidae), Journal of Stored Products Research 35, no.33 (Jul 1999): 197–213.https://doi.org/10.1016/S0022-474X(99)00005-3R.M.M. Traynier, R.K. Schumacher Yeast odours localize oviposition by Tinea translucens and T. pellionella (Lepidoptera: Tineidae), Journal of Stored Products Research 31, no.44 (Oct 1995): 301–305.https://doi.org/10.1016/0022-474X(95)00026-4R.M.M. Traynier, R.K. Schumacher, D.M. Lau Oviposition site selection by Tineola bisselliella, Tinea spp (Lepidoptera: Tineidae) and Anthrenus flavipes (Coleoptera: Dermestidae), Journal of Stored Products Research 30, no.44 (Oct 1994): 321–329.https://doi.org/10.1016/S0022-474X(94)90323-9DENIS L. FOX PIGMENT TRANSACTIONS BETWEEN ANIMALS AND PLANTS, Biological Reviews 54, no.33 (Aug 1979): 237–268.https://doi.org/10.1111/j.1469-185X.1979.tb01012.xPritam Singh Lepidoptera, (Jan 1977): 287–453.https://doi.org/10.1007/978-1-4684-8349-9_11P.J. Herring The carotenoid pigments of Daphnia magna straus—II. Aspects of pigmentary metabolism, Comparative Biochemistry and Physiology 24, no.11 (Jan 1968): 205–221.https://doi.org/10.1016/0010-406X(68)90968-7R. Beutler Vergleichende Physiologische Chemie, (Jan 1966): 659–970.https://doi.org/10.1007/978-3-662-37018-6_2L. R. FISHER, S. K. KON Vitamin a in the Invertebrates, Biological Reviews 34, no.11 (Feb 1959): 1–36.https://doi.org/10.1111/j.1469-185X.1959.tb01300.xH. E. Hinton The Larvae of the Species of Tineidae of Economic Importance, Bulletin of Entomological Research 47, no.22 (Jul 2009): 251–346.https://doi.org/10.1017/S0007485300046708H.-J. Bielig Carotinoide und A-Vitamine, (Jan 1955): 954–1068.https://doi.org/10.1007/978-3-662-28629-6_14Henrik Dam The biochemistry of fat-soluble vitamins, Progress in the Chemistry of Fats and other Lipids 3 (Jan 1955): 153–212.https://doi.org/10.1016/0079-6832(55)90006-9Howard L. House Nutritional Studies with Blattella germanica (L.) Reared Under Aseptic Conditions: III. Five Essential Amino Acids, The Canadian Entomologist 81, no.66 (May 2012): 133–139.https://doi.org/10.4039/Ent81133-6WILLIAM TRAGER INSECT NUTRITION, Biological Reviews 22, no.22 (Apr 1947): 148–177.https://doi.org/10.1111/j.1469-185X.1947.tb00327.x Insect Pests of Food, and the Consumer, by R. V. WADSWORTH, F.R.I.C., F.R.E.S., Chief Chemist, Cadbury Brothers, Ltd, Journal of the Royal Sanitary Institute 65, no.33 (Sep 2016): 150–159.https://doi.org/10.1177/146642404506500303R. S. Hartley, F. F. Elsworth, J. Barrritt The Mothproofing of Wool, Journal of the Society of Dyers and Colourists 59, no.1212 (Oct 2008): 266–271.https://doi.org/10.1111/j.1478-4408.1943.tb02211.xGeorge Wald The Photoreceptor Function of the Carotenoids and Vitamins A, (Jan 1943): 195–227.https://doi.org/10.1016/S0083-6729(08)60255-1

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  • A D Imms

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(A) Roaches (Blattella germanica L.) can be conveniently reared in large numbers by using a simple rearing cage which is described. The technique employed in rearing these insects is given. (B) The webbing clothes moths (Tineola biselliella Hummel) have been reared very easily in small containers housed in an insectary. The methods used in rearing large numbers of clothes moths is described. (C) The common bean weevil (Bruchus obtectus Say), the rice weevil (Sitophilus oryza L.), and the confused flour beetle (Tribolium confusum Fab.) were reared in large tin drums kept in an insectary. The simple procedures employed in rearing these insects are given.

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Potentials of a biogenic residue-based production ofHermetia illucens as fish meal replacement in aquafeed forOncorhynchus mykiss in Germany
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Owing to an increasing world population and a rising demand in protein for food and feed, alternative protein sources are needed. In addition, existing food and protein supplies such as wild and farmed fish need to be secured. Insects and more specifically the black soldier fly (BSF;Hermetia illucens) larvae, are discussed as an alternative animal protein source and a potential fish meal (FM) replacer in aquaculture. They can be sustainably reared on biogenic residues. In a literature study, the technical potential of occurring biogenic residues in Germany for the production of BSF larvae is estimated and their suitability as a FM replacement in aquafeed for the production of rainbow trout is evaluated. According to literature, up to 50% of FM can be substituted by BSF larvae meal in the feed of rainbow trout. For the annual German rainbow trout production of 8,466 t, 2,699 t BSF larvae meal (40.7% protein d.m.) is required to replace 1,556 t FM (70.9% protein d.m.). The demand for biogenic residues to feed the BSF larvae amounts to 22,942 t (d.m.). A large amount of biogenic residues occurring in Germany, such as forestry residues, animal excrements, straw and the biogenic fraction of municipal waste, have too poor nutrient contents or are inapplicable due to legal restrictions as feed for farmed animals. However, an alternative utilisation of approximately 1.26 Mt (d.m.) of biogenic industrial residues by far exceeds the demand for BSF larvae feed. Further investigations are needed on the environmental impact and profitability of using biogenic residues for BSF larvae production and competing utilisation pathways as well as of using resulting BSF larvae meal as FM replacement in feed for rainbow trout. Graphical abstract – Annual technical potential of a biogenic residue-based production of black soldier fly (BSF) larvae as aquafeed for farmed rainbow trout in Germany (M = million, based on dry weight unless indicated otherwise).

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