Nomenclature & Description

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Phyllomyza Fallén

Diagnosis: 

3 lateroclinate orbital setae; posteroventral comb of setae on the first tarsomere of the hind leg; usually greatly enlarged palpus and basoflagellomere in males

Original genus: 
Phyllomyza
Author: 
Fallén
Year: 
1810
Parentheses: 
Absent
Page: 
20
Type data: 

securicornis Fallén (SM)

Status: 
valid
Valid genus: 
Phyllomyza
Synonyms: 
Hendelimyza Duda, 1935
BDWD_rec_number: 
5222
Distribution: 

Absent in the Neotropical and rare in the Oceanic Region but occurs in all other regions. In Middle Europe Phyllomyza is the most species rich genus of Milichiidae and can be collected in open grasslands with scattered short trees or bushes, like for example in dunes.

Biology: 

Several species are known to be myrmecophilous, with the larvae developing in ant's nests

Discussion: 

Page with photos of male heads for comparison, see here

Milichiella Giglio-Tos

Diagnosis: 

Usually differs from other genera of Milichiinae in the combination of posterior eye margin with notch and/or emargination and posteromedial triangular projection of male T1 into T2. A group of Milichiella species
in which neither of these character states is present can be differentiated from other Milichiinae by the following combination of characters: Nearctic or Neotropical distribution, 2 frontal setae, posterior eye margin gradually separating from head margin ventrally, and anepisternum bare.

Original genus: 
Milichiella
Author: 
Giglio-Tos
Year: 
1895
Parentheses: 
Absent
Page: 
367
Type data: 

Tephritis argentea Fabricius, 1805: 323 [mon.; a misidentification of the species, which was described later as Milichiella tosi Becker, 1907; see Sabrosky 1973: 4]

Status: 
valid
Valid genus: 
Milichiella
Synonyms: 
Ophthalmomyia Williston, 1896; Stenoporomyia Hendel, 1903; Eccoptomma Becker, 1907; Ulia Becker, 1907; Pareccoptomma Duda, 1935
BDWD_rec_number: 
5215
Coloration and vestiture: 

Head and thorax usually brown, black or grey, sometimes with special colour patterns; lunule usually black, sometimes brown or yellow; basoflagellomere usually black, sometimes basomedially yellow to red; face usually brown or greyish microtomentose, sometimes silvery; palpus usually black, sometimes yellow to red; thorax with mesonotum in all variations between shiny and strongly microtomentose; wing and calypter usually hyaline, sometimes white or brownish; brown spot at apex of vein R1 absent to strong, halter colour often different in males and females, male abdomen usually black in ground colour, rarely yellow; male T2-5 often with silvery microtomentum in various patterns; female T2-5 usually brown or black.

Head: 

Frons with 2-3 orbital and 2-3 frontal setae; frons in males narrower than in females; posterior eye margin usually but not always with notch and narrow emargination.

Thorax: 

1-5 dc, 1-5 prsc, 1-2 pprn, 1 prs to row of prs across mesonotum, usually 2 main keps and some smaller setae.

Wing: 

Wing with R4+5 and M parallel to strongly convergent.

Legs: 

Tibial organ rarely present.

Male abdomen: 

Posteromedial triangular projection of T1 into T2 usually but not always present; T2 anterolateral corner often with tuft of setae; T2-5 usually with lateral, less sclerotized crease where tergites are bent ventrally; shape and setation of S5 species-group specific; genitalia usually with 1 seta on subepandrial plate, shape, lateral structure and setation of surstylus species or species-group specific.

Female abdomen: 

Preabdomen typical for Milichiidae. Shape of S4 and S5 varies and could possibly be species-group specific. However, females are unknown or questionable for most species. Ovipositor long and retractable; T6-8 and S6-7 complete, S8 longitudinally divided, cerci usually paired but fused in Milichiella iberica Carles-Tolrá (Carles-Tolrá 2001) and possibly dorsally fused in some other species (M. bakeri Aldrich, M. mexicana Brake). Spermathecal ducts rolled up into one longish coil or with very tightly wound, spindle-like coil (Brake 2000).

Length: 
1.6–4.7 mm
Egg: 

Shape elongate, narrower anteriorly. Chorionic sculpture consists of minute, rounded pits in M. tiefii and M. lasuizae sp. n.; M. lacteipennis with even smaller pits. Pits arranged in more or less distinct hexagonal fields in M. tiefii (Roháček 1995). Micropyle connected by radial ribs with surrounding ring in M. tiefii; radial ribs also visible in M. lacteipennis. (Roháček 1995, Brake 2009)

Larva: 

(Milichiella tiefii, after Roháček 1995): Slender, elongate, narrower on anterior quarter. Cephaloskeleton with slender, strongly sclerotized mouthhooks, with sharply pointed apex and narrow, relatively acute posteroventral apodeme. Dental sclerite rounded tetragonal, weakly sclerotized. Intermediate sclerite separate from basal sclerite, relatively robust; lateral rods strongly sclerotized and connected by slender, strip-like cross-bridge. Complex labial sclerite in front of cross-bridge composed of posterior convex plate bearing 2 lateral (anteriorly-directed) and 2 small medial projections, and anterior slender, v-shaped sclerite (the latter perhaps homologous with ligulate sclerite). Epistomal sclerite (situated anterodorsally between arms of intermediate sclerite) membraneous, with only margins of 2 small perforations pigmented and thereby visible, even in ventral view. Parastomal bars very slender but dark and heavily sclerotized. Basal sclerite very pale, weakly sclerotized, except for anterior part. Dorsal bridge simple, not separated by incision from rest of basal sclerite. Dorsal cornua slender, posteriorly pointed, essentially smaller than ventral cornua; the latter long and broad but without dorsal apodeme. Ventral cornua joined ventrally by downward curving trough with conspicuous, longitudinal ridges. Cephalic region bilobate, with antenna dorsally near apex of each lobe; facial mask bearing oral ridges. Anterior spiracle with 7 digitiform protuberances arranged in flattened, semirosette shape. Posterior spiracles borne on widely separated protuberances; each spiracle without peritreme and not on single plate, but composed of 3 pale yellowish brown, finger-like projections. Each spiracular projection has its own, slightly curved slit and several, slightly ramifying, fine peristigmatal tufts.

Puparium: 

Elongate, tapering towards anterior and posterior end. Empty puparium yellow to reddish brown, subshiny to dull, with distinct border between segments. All thoracic segments sculptured by distinctive, mostly transverse ribs; prothoracic (both dorsally and ventrally) and mesothoracic (dorsally only) segments with more conspicuous ribbed sculpture. Anterior spiracles with 6-9 (6 in Milichiella lacteipennis, 7 in M. tiefii and 9 in M. asiatica Brake) spiracular lobes (papillae). Abdominal segments circled by very fine ribs or wrinkles, ventrally each with 1-3 transverse rows of very minute spinulae. Posterior end of puparium more convex and strongly transversely or reticularly (last segment) ribbed. Anus visible. For posterior spiracles see larval description. (Roháček 1995, Brake 2009)

Distribution: 

worldwide

Biology: 

Specimens have been reared from various decaying fruit, vegetables or other vegetation (Milichiella near argentiventris Hendel, M. asiatica, M. circularis Aldrich, M. hendeli Brake var., M. lacteipennis, M. novateutoniae Brake, M. quintargentea Brake, and M. unicolor (de Meijere)), with several species of the argentea-group having been caught or reared from palms (Aracaceae). Most species of the aethiops-group, as well as Milichiella acantha Brake and Milichiella sp. L, have been reared from cacti (Cactaceae), e.g. Cereus giganteus, Echinocactus polycephalus, Lophophora williamsii (peyote), Myrtillocactus geometrizans, Myrtillocactus sp., Opuntia occidentalis, Opuntia (Platyopuntia) sp., Pachycereus sp., and Pachycereus schottii. Milichiella aethiops was also reared from “wild tuber”. At least four species (Milichiella argyrogaster, M. cinerea (Coquillett), M. tiefii, and M. urbana Malloch) develop in rotting bark or wood (beech, lime, poplar), which probably needs to be infested first by bark beetles. For details on the biology of Milichiella tiefii, see Roháček (1995).

Various species have been observed on or near plants, e.g. Pandanus (Pandanaceae) (Milichiella aldabrae Brake), Murraya exotica (Rutaceae) (M. argenteocincta Johnson), Croton sp. (Euphorbiaceae) (Milichiella sp. B), cotton (Malvaceae) (M. zaiziksensis Brake var.), baobab (Malvaceae) (M. unicolor), yucca (Agavaceae) (M. zaiziksensis), Cassia leaf (Fabaceae) (M. nudiventris Becker), Shorea macrophylla and S. johorensis (Dipterocarpaceae) (M. bruneiensis Brake), and pawpaw (Asimina, Annonaceae) (M. lacteipennis). Some specimens were observed on flowers, possibly pollinating, e.g. Euphorbia regis-jubae (Euphorbiaceae) and Schinus mollis (Anacardiaceae) (M. bimaculata Becker, M. lacteipennis), Ipomoea tiliacea (Convolvulaceae) (M. cingulata), Lactuca scariola var. integrata (Asteraceae) (M. arcuata), Tamarix gallica L. (Tamaricaceae) and Lonicera (Caprifoliaceae) (M. hendeli), Donnellsmithia hintonii, Asclepias, Baccharis glutinosa, Ochradenus baccatus (Resedaceae), Cocos nucifera (Arecaceae) and Polyscias scutellaria (Araliaceae) (M. lacteipennis), Thapsia villosa (Apiaceae) (M. iberica).

Some species were collected on or near mushrooms or mushroom compost, e.g. Milichiella aldabrae, Milichiella arcuata (Loew) var., and Milichiella lucidula Becker.

Milichiella argenteocincta was found in dirt near an Atta cephalotes nest and reared from excrement in a toucan's nest. Milichiella longirostris Brake and ?Milichiella arcuata var. emerged from the detritus of a gopher tortoise burrow and M. arcuata has been reared from a chicken pen. Other species have been collected or reared from manure and dung of various herbivores or omnivores (Milichiella asiatica, M. lacteipennis, and M. quintargentea Brake), and two species were collected on carrion (M. arcuata, M. lacteipennis). Milichiella cavernae Brake, M. rugosistyla Brake and M. weejasperensis Brake were collected in caves, with the first being reared from bat dung.

Milichiella arcuata is attracted to [E]-2-hexenal and Milichiella sp. prob. lacteipennis to Podisius maculiventris pheromone. Milichiella lacteipennis was observed among aphids on cotton and feeding on bugs, usually Pentatomidae, caught by spiders (Nezara viridula, Nephila inaurata).

Swarming behaviour has been observed in males of M. bermaguiensis Brake, M. circularis, M. frontalis (Becker), M. hendeli, M. lacteipennis, M. longiseta Hardy & Delfinado, M. nigeriae nigeriae (Duda), M. sumptuosa de Meijere, M. tiefii, M. unicolor and M. zaiziksensis. These swarms were sometimes located above or close to the breeding substrate.

For more details or the citations see the comprehensive catalog or remarks section of the respective species.

Neophyllomyza inimica Séguy

Original genus: 
Neophyllomyza
Species epithet: 
inimica
Author: 
Séguy
Year: 
1938
Parentheses: 
Absent
Page: 
364
Type data: 

Kenya. Marakwet, Elgeyo Escarpment, 2500 m (T 1M MNHNP)

Status: 
valid
Valid genus: 
Neophyllomyza
Valid species: 
inimica
Other Information: 
This species belongs to the genus Phyllomyza
BDWD_rec_number: 
83725
Distribution: 

Kenya

Ulia Becker

Diagnosis: 

posterior eye margin with emargination; frons and mesonotum sculptured; hind tibia with tibial organ

Original genus: 
Ulia
Author: 
Becker
Year: 
1907
Parentheses: 
Absent
Page: 
544
Type data: 

poecilogastra Becker (MO)

Status: 
invalid (junior objective synonym)
Valid genus: 
Milichiella
Other Information: 
Syn. Brake (2009)
BDWD_rec_number: 
10935
Distribution: 

South America

Biology: 

unknown

Xenophyllomyza deserticola Ozerov

Original genus: 
Xenophyllomyza
Species epithet: 
deserticola
Author: 
Ozerov
Year: 
1992
Parentheses: 
Absent
Page: 
18
Type data: 

Turkmenistan. Batchiz (HT M ?)

Status: 
valid
Valid genus: 
Xenophyllomyza
Valid species: 
deserticola
BDWD_rec_number: 
115788
Distribution: 

Turkmenistan

Xenophyllomyza Ozerov

Diagnosis: 

Crossvein dm-cu absent; lunule bare

Original genus: 
Xenophyllomyza
Author: 
Ozerov
Year: 
1992
Parentheses: 
Absent
Page: 
18
Type data: 

deserticola Ozerov (OD)

Status: 
valid
Valid genus: 
Xenophyllomyza
BDWD_rec_number: 
17864
Distribution: 

Turkmenistan

Stomosis vittata Malloch

Original genus: 
Stomosis
Species epithet: 
vittata
Author: 
Malloch
Year: 
1925
Parentheses: 
Absent
Page: 
89
Type data: 

Australia. New South Wales: Sydney (HT F AMS)

Status: 
valid
Valid genus: 
Stomosis
Valid species: 
vittata
BDWD_rec_number: 
89567
Distribution: 

Australia

Stomosis rufula (Frey)

Original genus: 
Siphonomyiella
Species epithet: 
rufula
Author: 
Frey
Year: 
1918
Parentheses: 
Present
Page: 
18
Type data: 

Brazil. Rio de Janeiro (HT M UZMH)

Status: 
valid
Valid genus: 
Stomosis
Valid species: 
rufula
BDWD_rec_number: 
40798
Distribution: 

Brazil

Stomosis luteola (Coquillett)

Original genus: 
Desmometopa
Species epithet: 
luteola
Author: 
Coquillett
Year: 
1902
Parentheses: 
Present
Page: 
188
Type data: 

USA. Arizona: Williams (HT A USNM)

Status: 
(Available, Invalid) Junior Synonym
Valid genus: 
Stomosis
Valid species: 
innominata
BDWD_rec_number: 
40797

Stomosis innominata (Williston)

Original genus: 
Agromyza
Species epithet: 
innominata
Author: 
Williston
Year: 
1896
Parentheses: 
Present
Page: 
443
Type data: 

Saint Vincent and the Grenadines. St. Vincent (HT M BMNH)

Status: 
valid
Valid genus: 
Stomosis
Valid species: 
innominata
Synonyms: 
Desmometopa luteola Coquillett, 1902
BDWD_rec_number: 
67682
Distribution: 

Brazil, Colombia, Costa Rica, El Salvador, Honduras, Mexico, Panama and Canal Zone, West Indies [St. Vincent, Trinidad]; Arizona

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