Bama McAlpine, 2001

McAlpine, David K., 2015, Signal Flies of the Genus Bama (Diptera: Platystomatidae) in Papua New Guinea, Records of the Australian Museum 67 (2), pp. 25-53 : 25-26

publication ID

https://doi.org/ 10.3853/j.2201-4349.67.2015.1603

persistent identifier

https://treatment.plazi.org/id/03AB6A52-FFE3-562D-FC56-D60EFFD8028B

treatment provided by

Carolina

scientific name

Bama McAlpine
status

 

Genus Bama McAlpine View in CoL

Bama McAlpine, 2001: 165–166 View in CoL . Type species (original designation) Xiria papuana Hennig. View in CoL

Relationships and identification. Hendel (1914a,b) recognized a subtribe Cleitamiina to include the New Guinea genera Loriomyia Kertész View in CoL , Cleitamia Macquart, and Laglaisia Bigot View in CoL , which he separated from some other platystomatine taxa in his key (1914b: 8) by having the crossveins (anterior and discal) strongly approximated, tergite 5 of male abdomen with some long posteriormarginal bristles, and the squama (or lower calypter) small. The genus Loriomyia View in CoL (j. syn. Agnostophana Hering ) must now be excluded as belonging in the family Tephritidae ( Korneyev, 2001) View in CoL , although convergent in some venational characters with Cleitamia View in CoL . The New Guinea genera Cleitamoides Malloch View in CoL and Bama View in CoL also belong in this Cleitamia View in CoL alliance. However, I do not at present recognize formal tribes or subtribes within the subfamily Platystomatinae View in CoL (as delimited by McAlpine, 1973, 2001), to which the four genera of this alliance belong.

Examples of the genus Bama can generally be determined as such by means of the key to Australasian platystomatid genera given by McAlpine (2001), where Bama occurs in three places, according to the combination of diagnostic characters possessed by the various species. Some significant character states for the genus are here given, though, as indicated, some of these are not present in all included species.

• Two pairs of fronto-orbital bristles present. This condition occurs in many platystomatine genera, but its consistent presence helps to distinguish Bama spp . from the apparently related Laglaisia spp., which consistently have a single, large fronto-orbital pair.

• Face (fused prefrons and clypeus—see McAlpine, 2007a) without central, steep-sided, platform-

like carina. Such carina is generally present in

the platystomatine genera Euprosopia Macquart , Lamprogaster Macquart , Achias Fabricius , and Duomyia Walker.

• Antennal segment 6 (occupying most of length of arista) with fairly uniform armature of non-dense short hairs (or long pubescence). Bama signifer n.sp. is exceptional, totally lacking these hairs.

• Stem vein (base of R) with fine, usually black dorsal setulae (see Fig. 37 View Figures 37, 38 ). Setulae in this position are present in all known Bama spp . except B. shinonagai McAlpine and B. robertsi n.sp. They are generally present in the genera Euprosopia and Pterogenia Bigot , which are not closely related to Bama , but are quite rarely present in other platystomatids.

• Anal cell (cup) of wing largely bare, usually with small distal zone of microtrichia and linear anterior marginal microtrichose stripe. In related genera (including Laglaisia, Cleitamia ) the membrane of the anal cell is generally extensively or entirely microtrichose.

• Squama (lower calypter) reduced. It is significantly smaller than in Euprosopia , Lamprogaster , Pterogenia , and most Achias spp. In B. shinonagai the squama is less reduced than in other Bama spp ., but still occupies less than a semicircle in relation to its basal line of attachment to the thorax.

• Anterior plate of mid coxa laterally with two differentiated black bristles and mesad of these a marginal comb of finer setulae. This is a common condition in many platystomatid genera, but the major bristles are less distinct in Achias , Lamprogaster , and many Euprosopia spp. There are specific differences in the marginal comb among Bama spp .

• Mid tibia with one large terminal ventral spur much longer than tibial diameter, any additional spurs

being very small. This condition is diagnostic for the Cleitamia alliance as above delimited, most other platystomatids having the mid-tibial spur relatively short. However, in Euxestomoea de Meijere there are two long apical spurs on the mid tibia.

• In female, abdominal tergite 3 enlarged; tergites 4

and 5 much reduced in size and often more or less concealed in dried specimens. This is one of the most marked diagnostic traits for the genus Bama , and does not occur in Cleitamia , Cleitamoides, Laglaisia , and any other platystomatine genus of Australasia.

• In male, aedeagus with pair of tapering terminal filaments of unequal size, arising from apex of elongate bulb. The cuticle of both filaments bears closely placed sclerotized rings on most of its length. The unequal size of the terminal filaments seems to distinguish Bama from species of the related genera Cleitamia , Cleitamoides , and Laglaisia, so far as

this has been observed. Unequal pairs of terminal filaments occur in a few species of Lamprogaster (see McAlpine, 1973) and Euprosopia ( McAlpine, 2007b) , but the aedeagus of such species does not otherwise resemble that of Bama spp .

In the present study, I have slightly altered the terminology for parts of the aedeagus from that used previously ( McAlpine, 2001: figs 75, 78). The part immediately preceding the glans is now termed the flexible section of the aedeagus, instead of the preglans, and the variably differentiated part preceding this is termed the preglans ( Figs 41 View Figures 39–41 , 46 View Figures 45–47 , in accordance with my more recent studies of Duomyia spp. ( McAlpine, 2011: fig. 1).

Abdominal tergite 5 in males of Bama spp . generally has the posterior-marginal bristles less enlarged than in Cleitamia and Laglaisia.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Diptera

Family

Platystomatidae

Loc

Bama McAlpine

McAlpine, David K. 2015
2015
Loc

Bama

McAlpine, D 2001: 166
2001
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