Phoridae

Life-forms

Superregnum: Eukaryota
Cladus: Unikonta
Cladus: Opisthokonta
Cladus: Holozoa
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Cladus: Protostomia
Cladus: Ecdysozoa
Cladus: Panarthropoda
Phylum: Arthropoda
Subphylum: Hexapoda
Classis: Insecta
Cladus: Dicondylia
Subclassis: Pterygota
Cladus: Metapterygota
Infraclassis: Neoptera
Cladus: Eumetabola
Cladus: Endopterygota
Superordo: Panorpida
Cladus: Antliophora
Ordo: Diptera
Subordo: Brachycera
Infraordo: Muscomorpha
Sectio: Aschiza
Superfamilia: Phoroidea

Familia: Phoridae
Subfamiliae (6): Metopininae - Phorinae - Prioriphorinae - Sciadocerinae - Termitoxeniinae - Thaumatoxeninae

Overview of genera (282)

Abaristophora – Acanthophorides – Achaetophora – Acontistoptera – Adelopteromyia – Adenophora – Aemulophora – Aenictacantha – Aenictomyia – Aenigmaphora – Aenigmatias – Aenigmatistes – Aenigmatopoeus – Alamira – Allochaeta – Anaclinusa – Anevrina – Anticofimbria – Aphiura – Apocephalus – Apodicrania – Apopteromyia – Apterella – Apterophora – Aptinandria – Arabiphora – Archiphora – Aristocerina – Arrenaptenus – Assmutherium – Auxanommatidia – Beckerina – Billotia – Bolsiusia – Borgmeieriphora – Borophaga – Bothroprosopa – Brachycephaloptera – Brachycosta – Brachyphlebina – Brachyselia – Brevrostrophora – Brownphora – Burmophora – Calamiscus – Cataclinusa – Ceratoconus – Ceratophoromyia – Ceratusa – Ceylonoxenia – Chaetaspidia – Chaetogodavaria – Chaetopleurophora – Cheiloxenia – Chelidophora – Chonocephalus – Clinochaeta – Clitelloxenia – Colobomeles – Colyeria – Commoptera – Conicera – Coniceromyia – Contopteryx – Cootiphora – Corynusa – Crasilla – Cremersia – Cryptophora – Ctenopleuriphora – Cyphocephalus – Cyphometopis – Cyrtophorina – Dacnophora – Dahliphora – Danumphora – Darwiniphora – Diaclinella – Dichocerina – Dicranodeina – Dicranopteron – Dinocercus – Diocophora – Diplonevra – Diplostylocera – Distichophora – Dohrnigma – Dohrniphora – Dorsochaeta – Dundophora – Echidnophora – Ecitomyia – Ecitophora – Ecitoptera – Ecituncula – Ectochaeta – Egregiophora – Enderleinphora – Endonepenthia – Epacteon – Epactoselia – Epichonocephalus – Epicnemis – Eremophora – Eurycnemis – Euryphora – Euryplatea – Eutermiphora – Exochaeta – Franssenia – Godavaria – Gymnophora – Gymnoptera – Haplophleba – Haulepta – Hexacantherophora – Hieronymus – Hirotophora – Holopterina – Homalophora – Horologiphora – Hylophora – Hypocera – Hypocerides – Hypogeophora – Idiophora – Iridophora – Javanoxenia – Johowia – Kerophora – Kierania – Kuenburgia – Laciniomyia – Laishania – Latiborophaga – Lecanocerus – Lenkoa – Lepta – Leptilla – Lobochaeta – Lucianaphora – Macrocerides – Macroselia – Maculiphora – Mallochphora – Mannheimsia – Megapropodiphora – Megaselia – Melaloncha – Melittophora – Menozziola – Metopina – Miclepta – Microplatyphora – Microselia – Minicosta – Misotermes – Mollicauda – Morahania – Multinevra – Myopiomyia – Myriophora – Myrmosicarius – Neodohrniphora – Neophora – Obscuriphora – Odontoxenia – Oligophora – Pachyneurella – Pallura – Palpiclavina – Palpocrates – Paraphiochaeta – Paraphiura – Parasyneura – Paratermitoxenia – Paurophora – Pelidnophora – Penthaplus – Pericyclocera – Pericyclocerina – Perissa – Perittophora – Peromitra – Phalacrotophora – Pheidolomyia – Phlebothrix – Phora – Phoricesa – Phymatopterella – Physoptera – Pilosaphiura – Placophorina – Plastophora – Plastophorides – Platydipteron – Plectanocnema – Plethysmochaeta – Pleurophorina – Poloniphora – Postoptica – Pradea – Procliniella – Pronudiphora – Pseudacteon – Pseudohypocera – Pseudotermitoxenia – Psyllomyia – Ptochomyia – Puliciphora – Razorfemora – Rhabdomyia – Rhopica – Rhynchomicropteron – Rhyncophoromyia – Ridiculiphora – Ritchiephora – Sciadocera – Septemineophora – Siluphora – Sinogodavaria – Sphinctomyia – Spiniphora – Stenoneurellys – Stenophorina – Stethopathusa – Stichillus – Styletta – Synaptophora – Synclinusa – Syneura – Syneurina – Syntermitoxenia – Syntermophora – Tabelliphora – Tapantia – Tarsocrates – Tayrona – Teratophora – Termitomyia – Termitophilomyia – Termitophorides – Termitophorina – Termitosagma – Termitoscrofa – Termitosphaera – Termitostroma – Termitoxenia – Thalloptera – Thaumatoxena – Tonnoirina – Tranopeltoxenos – Travassophora – Trichocerina – Trineurocephala – Triphleba – Trispiniphora – Trophithauma – Trophodeinus – Tropophleba – Trucidophora – Tubicera – Tubiceroides – Veranophora – Veruanus – Vestigipoda – Volvectiphora – Wandolleckia – Wharia – Woodiphora – Woodiphorides – Xanionotum – Xenophoromyia – Xenotriphleba – Zikania – Zygtaxphora – †Agaphora – †Archisciada – †Eosciadocera – †Euliphora – †Hennigophora – †Jealia – †Prioriphora – †Ulrichophora

[source: Catalogue of Life: 2011 Annual Checklist, minus (2) Ceratoplatus – Musca
, plus (10) Minicosta – Phoricesa – Wharia – †Agaphora – †Archisciada – †Eosciadocera – †Euliphora – †Hennigophora – †Jealia – †Prioriphora
, and Ulrichophora
to †Ulrichophora
]

Check: Chaetocnemistoptera – Neopleurophora
Name

Phoridae
Synonyms

Sciadoceridae

References

Ament, D.C. 2018. Taxonomic revision of the genus Hirotophora Brown et al. (Diptera: Phoridae) with the description of a new species from Chile. Zootaxa 4394(4): 549–558. DOI: 10.11646/zootaxa.4394.4.5 Reference page.
Borgmeier, T. 1968: A catalogue of the Phoridae of the World (Diptera, Phoridae). Studia entomologica, 11: 1–367. [not seen]
Brown, B.V. 1992: Generic revision of Phoridae of the Nearctic Region and phylogenetic classification of Phoridae, Sciadoceridae and Ironomyiidae (Diptera: Phoridea). Memoirs of the Entomological Society of Canada, 164: 1–144.
Brown, B.V., 2001: Taxonomic revision of Neodohrniphora, subgenus Eibesfeldtphora (Diptera: Phoridae). Insect Systematics & Evolution 32 (4): 393–409. Abstract: DOI: 10.1163/187631201X00272.
Brown, B.V. 2007: A further new genus of primitive phorid fly (Diptera: Phoridae) from Baltic amber and its phylogenetic implications. Contributions in science (Los Angeles), (513 ) ISSN: 0459-8113 PDF
Brown, B.V. 2010: An enigmatic new genus and species of phorid fly from Baltic amber. Studia dipterologica, 16 (1/2): 43–46. PDF
Brown, B.V. 2018. A second contender for “world’s smallest fly” (Diptera: Phoridae). Biodiversity Data Journal 6: e22396. DOI: 10.3897/BDJ.6.e22396. Reference page.
Brown, B.V. & Porras, W. 2016. A second species, and first Central American record, of the phorid fly genus Lenkoa Borgmeier (Diptera: Phoridae). Zootaxa 4168(3): 583–588. DOI: 10.11646/zootaxa.4168.3.11. Reference page.
Cook, C.E.; Austin, J.J.; Disney, R.H.L. 2004: A mitochondrial 12S and 16S rRNA phylogeny of critical genera of Phoridae (Diptera) and related families of Aschiza. Zootaxa, 593: 1–11. PDF
Disney, R.H. 2009: Scuttle flies (Diptera: Phoridae) reared from logs in Finland and N. W. Russia, including two new species. Entomologica Fennica 20 (4): 257–267. Abstract: [1]
Disney, R.H.L. 2012: Scuttle flies (Diptera: Phoridae) caught at dead mice in S. W. Finland. Zootaxa 3298: 30–42. Preview Reference page.
Hartop, E., Brown, B.V. & Disney, R.H.L. 2015: Opportunity in our Ignorance: Urban Biodiversity Study Reveals 30 New Species and One New Nearctic Record for Megaselia (Diptera: Phoridae) in Los Angeles (California, USA). Zootaxa 3941(4): 1–451. DOI: 10.11646/zootaxa.3941.4.484. Preview Reference page.
Hash, J.M. & Brown, B.V. 2015. Revision of the New World Species of the Millipede-Parasitic Genus Myriophora Brown (Diptera: Phoridae). Zootaxa 4035(1): 1–79. DOI: 10.11646/zootaxa.4035.1.1. Preview (PDF) ISBN 978-1-77557-819-2 (paperback); ISBN 978-1-77557-820-8 (Online edition) Reference page.
Koçak, A.Ö.; Kemal, M. 2010: Nomenclatural notes on the genus group names of the order Diptera. Centre for Entomological Studies Ankara miscellaneous papers, 151: 5–7. Internet Archive
Kung, G.-A.; Brown, B.V. 2005: Three unusually divergent new genera of phorid flies (Diptera: Phoridae) from Costa Rica. Zootaxa, 1019: 43–52. Abstract & excerpt PDF PDF.
Liu, G-C. 2020. A new genus of the Hypocera group (Diptera, Phoridae), with descriptions of two new species from China. ZooKeys, 932: 113–127. DOI: 10.3897/zookeys.932.38970 Open access Reference page.
Liu, G.-C. & Q.-Q. Zeng, 1966: A Further New Species of Trophithauma From China (Diptera:Phoridae). Zoological Research 16 (4): 349–351.
García-Robledo, C.; Barrientos, J.A. 2014: Nine new species of Phoridae (Insecta: Diptera) from Spain. Zootaxa 3857(2): 244–260. DOI: 10.11646/zootaxa.3857.2.5 Reference page.

Additional references

Ament, D.C. & Brown, B.V. 2016. FAMILY PHORIDAE. In Wolff, M.I., Nihei, S.S. & Carvalho, C.J.B. de (eds.), Catalogue of Diptera of Colombia. Zootaxa 4122(1): 414–451. DOI: 10.11646/zootaxa.4122.1.37. Reference page.
Mostovski, M.B. 2016. A review of scuttle fly genera of Israel (Diptera: Phoridae), with new records and an identification key. Zootaxa 4137(1): 61–72. DOI: 10.11646/zootaxa.4137.1.4. Reference page.

Vernacular names
English: Phorid fly
suomi: Ryhäkärpäset
日本語: ノミバエ科
中文: 蚤蝇科

The Phoridae are a family of small, hump-backed flies resembling fruit flies. Phorid flies can often be identified by their escape habit of running rapidly across a surface rather than taking to the wing. This behaviour is a source of one of their alternate names, scuttle fly. Another vernacular name, coffin fly, refers to Conicera tibialis.[1] About 4,000 species are known in 230 genera. The most well-known species is cosmopolitan Megaselia scalaris. At 0.4 mm in length, the world's smallest fly is the phorid Euryplatea nanaknihali.[2]

Description

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For terms see Morphology of Diptera
Phora wing venation

Phorid flies are minute or small – 0.5–6 mm (1⁄64–1⁄4 in) in length. When viewed from the side, a pronounced hump to the thorax is seen. Their colours range from usually black or brown to more rarely yellow, orange, pale grey, and pale white. The head is usually rounded and in some species narrowed towards the vertex. The vertex is flat. In some species, the ocellar callus is swollen and highly raised above the surface of the vertex. The eyes are dichoptic in both males and females (eyes of males close-set, of females wide-set). The third segment of the antenna is large and rounded or elongated, and bears a long apical or dorsal arista directed sideways. The arista is glabrous or feathered. The third antennal segment in some species is unique in shape. Sexual dimorphism is often shown in the shape and size of third segment of antennae, and in males, the antennae are usually longer. The proboscis is usually short and sometimes with enlarged labella. The proboscis may be elongated, highly sclerotized, and bent at an angle. Maxillary palpi vary in shape and are sometimes large (species of genus Triphleba). The groups of bristles are developed on the head. Two pairs of supra-antenna1 bristles, sometimes one, are completely reduced. Above these are antenna1 bristles closer to (but still some distance from) the margin of eyes. Three bristles are spaced along the margin of eyes-anterolateral midlateral and posterolateral. Immediately before the ocellar callus are two preocellar bristles. The ocellar callus bears a pair of ocellar bristles and in some genera between the antennae and the preocellar bristles two additional, intermediate bristles occur.

The convex mesonotum is usually covered with hairs and rows of bristles. An important taxonomic character is the precise location of the anterior spiracles on the pleura of the thorax. The metapleuron may be entire or divided by a suture into two halves, and either with a few long bristles glabrous, or pubescent. The legs have stout femora and the hind femora are often laterally compressed.

The wings are clear or tinged only rarely with markings. They have a characteristic reduced wing venation. The strong, well developed radial (R) veins end in the costa about halfway along the wing. The other veins (branches of the medius) are weaker and usually follow a diagonal course and are often parallel to each other. Crossveins are totally absent. The costa reaches only to the point of confluence of alar margins with veins R4+5 or R5. The ratio of first, second, and third sections of the costa is often a reliable specific character. Other costal indices (compared to other wing measurements) are used in the taxonomy. Two rows of well developed bristles are present on the costa and almost at a right angle to each other. The subcosta is reduced. Of the radial veins, only R1 and R4+5 are developed. R4+5 may furcate at end. R4 and R5 may merge into the alar margin separately or continue as a single vein to the end. Medial veins are represented by M1, M2, and M4. The anal vein may reach the alar margin, or is greatly shortened or almost atrophied.

The abdomen consists of six visible segments. Segments VII to X comprise the genitalia of the male (hypopygium), and in the female the terminalia. In some genera, segments VII to X in the female are highly sclerotized and extended into a tube ("ovipositor"). Segments VII and VIII of the male are more or less sclerotized in the genus Megaselia, but otherwise mostly membranous. Tergite 9 the (epandrium) is highly developed and usually fused at least on one side with the hypandrium (sternite 9). Only in the genus Megaselia is the hypandrium more or less distinctly separated from the epandrium. Unpaired sclerites (ventrites) developed at the distal end of the hypandrium vary in shape. They may be flat, swollen, or other. Sclerites are always present near the base of the cerci, which may be highly developed, and converted either into a tube (anal tube) or a pair of asymmetrical large outgrowths (Phora). The phallosome is rarely complex in structure.

The larva is small, rarely over 10.0 mm long and typically has 12 visible segments. The shape varies from fusiform with inconspicuous projections on posterior segments to short, broad, and flattened with conspicuous dorsal and lateral plumose projections especially on the terminal segment. The colour is whitish, yellowish white, or grey. The first instar is metapneustic, later instars are amphipneustic.

Pupation occurs in the last larval skin which hardens and becomes reddish. The puparium is oval, pointed at ends (because the larval extremities remain relatively unchanged). Abdominal segment 2 has a dorsal pair of long, slender pupal respiratory horns.
Classification

Traditionally, phorids were classified into six subfamilies: Phorinae, Aenigmatiinae, Metopininae (including tribes Beckerinini and Metopinini), Alamirinae, Termitoxeniinae, and Thaumatoxeninae. Disney & Cumming (1992) abolished the Alamirinae when they showed they were the 'missing' males of Termitoxeniinae, which were known only from females.[3]

Also in 1992, Brown[4] presented a revised, cladistic classification based on many new character states. This classification included subfamilies Hypocerinae, Phorinae, Aenigmatiinae, Conicerinae, and Metopininae (Termitoxeniinae and Thaumatoxeninae were not included in his study). Disney rejected the entirety of Brown's work, deeming it premature, and a lively debate ensued.[5][6][7] Further resolution of this controversy awaits new data.

The oldest fossils of the family are known from Cretaceous aged amber, with the oldest known being from Early Cretaceous (Albian) French and Spanish amber.[8]
Biology
Phora sp. in copula

Phorid flies are found worldwide, though the greatest variety of species is to be found in the tropics. The Phoridae show the greatest diversity of all the dipterous families. Larvae are found in the nests of social insects and in some aquatic habitats, in organic detritus such as dung, carrion, insect frass, and dead snails. Some are synanthropic. Some species feed on bracket and other fungi and mycelium or on living plants (sometimes as leaf miners). Some are predators or parasites of earthworms, snails, spiders, centipedes, millipedes, and insect eggs, larvae, and pupae. The adults feed on nectar, honeydew, and the juices exuding from fresh carrion and dung. Some adults feed on the body fluids of living beetle larvae and pupae, others prey on small insects. Several species have the common name coffin fly, because they breed in human corpses with such tenacity, they can even continue living within buried coffins. For this reason, they are important in forensic entomology. Most commonly, they feed on decaying organic matter. Because they frequent unsanitary places, including drain pipes, they may transport various disease-causing organisms to food material. The adults are conspicuous on account of their fast and abrupt running. In some species, the males fly in swarms. Megaselia halterata, the mushroom phorid, is a pest of mushroom cultures. Although it does not cause direct damage, it is an efficient vector of dry mould (Lecanicillium fungicola).
Lifecycle

Phorid flies develop from eggs into larval, and pupal stages before emerging as adults. The female lays from one to 100 tiny eggs at a time in or on the larval food. She can lay up to 750 eggs in her lifetime. The time it takes from egg to adult varies on the species, but the average is about 25 days.

The larvae emerge in 24 hours and feed for a period between 8 and 16 days, before crawling to a drier spot to pupate. The phorid fly's egg-to-adult lifecycle can be as short as 14 days, but may take up to 37 days.

Many species of phorid flies are specialist parasitoids of ants, but several species in the tropics are parasitoids of stingless bees. These affected bees are often host to more than one fly larva, and some individuals have been found to contain 12 phorid larvae.[9]

Other species, especially those of the giant genus Megaselia, develop in various fungi during their larval stage and may be pests of cultivated mushrooms.[10]
Control of fire ants
Hooked ovipositor of Pseudacteon curvatus

Phorid flies also represent a new and hopeful means by which to control fire ant populations in the southern United States, where some species of fire ants were accidentally introduced in the 1930s. The genus Pseudacteon, or ant-decapitating flies, of which 110 species have been documented, is a parasitoid of ants. Pseudacteon species reproduce by laying eggs in the thorax of the ant. The first instar larvae migrate to the head, where they feed on the ant's hemolymph, muscle and nerve tissue. Eventually, the larvae completely devour the ant's brain, causing it to wander aimlessly for about two weeks.[11] After about two[12] to four[11] weeks, they cause the ant's head to fall off by releasing an enzyme that dissolves the membrane attaching the ant's head to its body. The fly pupates in the detached head capsule, requiring a further two weeks before emerging. Various species of Phoridae have been introduced throughout the southeast United States, starting with Travis, Brazos, and Dallas Counties in Texas, as well as Mobile, Alabama, where the non-native fire ants first entered North America.[11][12] The native species of fire ants are also parasitized by some species of Pseudacteon; these native fire ants don't cause ecological damage the way introduced species do.
Colony collapse disorder

In January 2012, a researcher discovered larvae in the test tube of a dead honey bee believed to have been affected by colony collapse disorder. The larvae had not been there the night before. The larvae were Apocephalus borealis, a parasitoid fly known to prey on bumblebees and wasps. The phorid fly lays eggs on the bee's abdomen, which hatch and feed on the bee. Infected bees act oddly, foraging at night and gathering around lights like moths. Eventually, the bee leaves the colony to die. The phorid fly larvae then emerge from the neck of the bee.[13]
Identification

Beyer, E.; Delage, A. Bearbeitet von: Schmitz, H. Phoridae 672 Seiten, 437 Abbildungen, 15 Tafeln, 26x19cm (in Erwin Lindner: Die Fliegen der Paläarktischen Region, Band IV / 7 Teil 1)1981 ISBN 3-510-43023-9
Borgmeier, T. 1963. Revision of the North American phorid flies. Part I. The Phorinae, Aenigmatiinae, and Metopininae, except Megaselia (Diptera: Phoridae). Stud. Entomol. 6:1–256. Keys subfamilies, genera and species.
Disney, R. H. L. (1994). Scuttle Flies: The Phoridae. London, Chapman & Hall. ISBN 978-0-412-56520-5.
Peterson B. V. (1987). Phoridae. In: Manual of Nearctic Diptera. Vol. 2. Canada Department of Agriculture Research Branch, Monograph no. 27, p. 689–712. The full text (53 MB) ISBN 0-660-12125-5 pdf
K. G. V. Smith, 1989 An introduction to the immature stages of British Flies. Diptera Larvae, with notes on eggs, puparia and pupae. Handbooks for the Identification of British Insects Vol 10 Part 14. pdf download manual (two parts Main text and figures index)

Other

A few cases of phorid flies opportunistically causing human myiasis have been reported.[14][15]
References

Colyer, C.N. (1954) The 'coffin fly', Conicera tibialis Schmitz (Dipt., Phoridae). Journal of the Society for British Entomology, 4, 203–206.
Brown, B.V. 2012: Small size no protection for acrobat ants: world's smallest fly is a parasitic phorid (Diptera: Phoridae). Annals of the Entomological Society of America, 105(4): 550–554. doi:10.1603/AN12011
Disney, R.H.L. & Cumming, M.S. (1992) Abolition of Alamirinae and ultimate rejection of Wasmann's theory of hermaphroditism in Termitoxeniinae (Diptera: Phoridae). Bonner zoologische Beiträge, 43, 145–154.
Brown, B.V. (1992). "Brown, B.V. 1992. Generic revision of Phoridae of the Nearctic Region and phylogenetic classification of Phoridae, Sciadoceridae, and Ironomyiidae (Diptera: Phoroidea)". Memoirs of the Entomological Society of Canada. 164: 1–144.
Disney, R.H.L. (1993) Mosaic evolution and outgroup comparisons. Journal of Natural History, 27, 1219–1221.
Brown, B.V. (1995) Response to Disney. Journal of Natural History, 29, 259–264.
Disney, R.H.L. (1995) Reply to Brown. Journal of Natural History, 29, 1081–1082.
Solórzano-Kraemer, Mónica M.; Bourdeau, Clément; Rosse-Guillevic, Simon; Hammel, Jörg U.; Xu, Chun-Peng; Brown, Brian V. (November 2021). "Parasitic hump-backed flies (Diptera: Phoridae) from Miocene ambers". Palaeoworld: S1871174X21000913. doi:10.1016/j.palwor.2021.11.002.
Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
Disney, R.H.L., Kurina, O., Tedersoo, L. & Cakpo, Y. (2013) Scuttle flies (Diptera: Phoridae) reared from fungi in Benin. African Invertebrates, 54 (2), 357–371.[1]
Hanna, Bill (May 12, 2009). "Parasitic flies turn fire ants into zombies". Fort Worth Star-Telegram. Archived from the original on May 22, 2009. Retrieved 2009-05-14.
"New weapon turns fire ants into headless zombies". San Francisco Chronicle. May 13, 2009. Archived from the original on May 16, 2009. Retrieved May 13, 2009.
A New Threat to Honey Bees, the Parasitic Phorid Fly Apocephalus borealis
T. L. Carpenter and D. O. Chastain: "Facultative Myiasis by Megaselia sp. (Diptera: Phoridae): A Case Report" in Journal of Medical Entomology, Vol. 29, No. 3 (1992), pp. 561–563.

K. Komori, K. Hara, K.G.V. Smith, T. Oda, D. Karamine: "A case of lung myiasis caused by larvae of Megaselia spiracularis Schmitz (Diptera: Phoridae)" in Transactions of the Royal Society of Tropical Medicine and Hygiene, Vol. 72 (1978), No. 5, pp. 467–470.

Disney, R. H. L. (1994). Scuttle Flies: The Phoridae. London, Chapman & Hall. ISBN 978-0-412-56520-5.
K. G. V. Smith, 1989 An introduction to the immature stages of British Flies. Diptera Larvae, with notes on eggs, puparia and pupae. Handbooks for the Identification of British Insects Vol 10 Part 14. pdf download manual (two parts Main text and figures index)