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Research Article
The genus Dettopsomyia Lamb, 1914 (Diptera, Drosophilidae) from southern China
expand article infoYa-Lian Wang§, Qiao Li§, Masanori J. Toda|, Jian-Jun Gao
‡ Yunnan University, Kunming, Kunming, China
§ Southwest Forestry University, Kunming, China
| Hokkaido University, Sapporo, Japan
¶ Yunnan University, Kunming, China
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Abstract

The genus Dettopsomyia was established by Lamb in 1914 for a single species, De. formosa described therein. It contains 13 known species recorded from the Old World (the Oriental, Australasian, Palearctic and Afrotropical regions). In the present paper, five new species discovered from southern China are described as members of Dettopsomyia: De. acutipenis Wang & Gao, sp. nov., De. serripenis Wang & Gao, sp. nov., De. discontinua Wang & Gao, sp. nov., De. camelonota Wang, Li & Gao, sp. nov. and De. paranigrovittata Wang, Li & Gao, sp. nov. The new species were delimitated, based on not only morphological characters but also molecular data.

Keywords

Dettopsomyia, DNA barcoding, new species, Styloptera, Yunnan

Introduction

The genus Dettopsomyia was established by Lamb (1914) for De. formosa described therein as the type species. Since then, a number of species have been added as new members to this genus or transferred from other genera by some authors, bringing the total number of known species in Dettopsomyia to 13. Duda (1926) described two Indonesian species, Dettopsomyia jacobsoni and De. acrostichalis, and transferred Drosophila pictipes de Meijere, 1911 from Indonesia and the Philippines into Dettopsomyia, together with Pictostyloptera preciosa (de Meijere, 1911) from Indonesia and Styloptera fruhstorferi Duda, 1924 from Vietnam. Wheeler (1951) transferred the Australasian species Drosophila nigrovittata Malloch, 1924 to Dettopsomyia. In addition, four more species, Dettopsomyia equscauda Takada & Momma, 1975 from Malaysia, De. philippina Takada, 1976 from the Philippines, De. alba Carson & Okada in Okada (1982) from Papua New Guinea and De. woodruffi Takada in Takada et al. (1990) from Kenya, have been described as new members of this genus, and two other species, Mycodrosophila bombax Burla, 1954 from Ivory Coast and Uganda and Styloptera repletoides Carson & Okada, 1980 from Papua New Guinea, have been transferred to Dettopsomyia by Tsacas (1980) and Okada (1982), respectively. Currently, a total of 13 species is assigned to this genus and are mainly distributed in the Old World tropics, i.e., the Oriental, Australasian and Afrotropical regions (Toda 2020).

From the early days of this taxonomic history, the status of the genus Dettopsomyia has been argued, especially in relation to the genus Styloptera Duda. Duda (1924) established the genus Styloptera for two new species, S. formosae Duda, 1924 and S. fruhstorferi Duda, 1924, and one known species, S. pictipes (de Meijere, 1911), transferred from the genus Drosophila Fallén, and the genus Pictostyloptera for Drosophila preciosa de Meijere, 1911. But later, Duda (1926) regarded both genera Styloptera and Pictostyloptera as synonymous with Dettopsomyia by finding intermediate morphologies between these genera in a study of Dettopsomyia formosa (the type species). Wheeler and Takada (1964) resurrected the genus Styloptera by choosing S. formosae as the type species because of its distinct morphology, but leaving De. fruhstorferi and De. pictipes in Dettopsomyia. Then, nine new species were added to the genus Styloptera by Okada and Carson (1980, 1983), Okada (1982) and Bock (1982), currently resulting in a total of ten species (Toda 2020). Wheeler and Takada (1964) and Bock (1982) gave the morphological diagnoses mostly on the head/thorax (color pattern and chaetotaxy) and the wing (color pattern and venation) for Dettopsomyia and Styloptera. However, some characters listed in the diagnoses were not contradictory between these two genera, but partially overlapping between them. Okada (1982) compared the morphology of the two genera in a revisional study covering 12 Dettopsomyia and eight Styloptera species. He listed some characters common to the two genera, e.g., wing costal lappet more or less developed and black, dorsocentral setae usually in three pairs, and frons and thorax usually ornamented, indicating close relationships between them. On the other hand, he proposed 13 characters (Table 1) as being diagnostic to distinguish between these two genera, at least for a few ‘representative’ species of them. However, none of these characters is applicable to most of the component species of either genus (Okada 1982). Bock (1982) argued that these two genera are closely related but most of their component species are very poorly known, and proposed that a complete revision of the two genera is necessary.

Table 1.

Diagnostic characters used to distinguish between the genera Dettopsomyia and Styloptera (adapted from Okada 1982).

Dettopsomyia Styloptera
Code State Code State
A Eye much oblique to the body axis. a Eye nearly rectangular to the body axis.
B Ocellar setae inserted inside triangle made by ocelli. b Ocellar setae inserted outside triangle made by ocelli.
C Anterior reclinate orbital minute. c Anterior reclinate orbital >> 1/3 as long as proclinate.
D Cheek not very broad, ~ 1/3 as broad as greatest diameter of eye. d Cheek very broad, ~ 2/3 as broad as greatest diameter of eye.
E Costal lappet large. e Costal lappet moderate.
F C-index < 1.0. f C-index > 1.0.
G R2+3 strongly curved to costa apically. g R2+3 straight or merely gently curved to costa.
H R4+5 and M1 divergent distally. h R4+5 and M1 parallel.
I Acrostichal bristles present. i Acrostichal bristles absent.
J Tibia ringed. j Tibia not ringed.
K Wing spotted. k Wing not spotted.
L Acrostichal setulae in 2 rows. l Acrostichal setulae in 4 or 6 rows.
M C3-fringe > 1/2. m C3-fringe < 1/2.

As Bock (1982) pointed out, the two genera Dettopsomyia and Styloptera are still less explored, making a full-scale revision of their phylogeny and taxonomy difficult. In the present paper, we describe five new species of Dettopsomyia discovered from China, and briefly address the ambiguity of Dettopsomyia and Styloptera in the systematics of the subfamily Drosophilinae.

Materials and methods

Specimens

Taxon sampling for morphological examination and DNA barcoding is shown in Table 2. The specimens were mostly captured by net sweeping above herbs in open forest, or at forest edge. Specimens were preserved in 70% (for morphological examination) or 100% ethanol (for DNA sequencing).

Table 2.

Summary of Dettopsomyia species and specimens examined in this study. Voucher numbers in bold indicate holotype specimens; gender of each specimen is given in parentheses, and GenBank accession numbers of COI sequences in brackets.

Species Collection site Collection date Voucher #
De. acutipenis sp. nov. Xishuangbanna Tropical Botanical Garden, Mengla, Xishuangbanna, Yunnan, China 19.iii.2006 #00138 (♀) [MZ645108], #00151 (♂)
18.iv.2007 #00380 (♀) [MZ645110], #00381 (♀) [MZ645111], #00382–386 (5♀)
16.iv.2007 #00387–389 (3♀)
De. serripenis sp. nov. Xishuangbanna Tropical Botanical Garden, Mengla, Xishuangbanna, Yunnan, China 19.iii.2006 #00152 (♂), #00155 (♂), #00156 (♀) [MZ645109], #00157 (♂), #00158 (♀)
24.iii.2006 #00153 (♂)
25.iii.2006 #00154 (♀)
De. discontinua sp. nov. Baihualing, Baoshan, Yunnan, China 4.viii.2012 #01139 (♂) [MZ645112], #01140 (♂) [MZ645113], #01141 (♂), #01142 (♂), #01143 (♀) [MZ645114], #01144 (♂) [MZ645115]
From rearings of R. decursiva infructescences collected from Baihualing, Baoshan, Yunnan, China 23.ix.2012 #01167–169 (3♀) [MZ645117–119], #01172–174 (3♂) [MZ645120–122]
Banpo, Yixiang, Simao, Pu’er, Yunnan, China 2.x.2012 #01584 (♂) [MZ645136], #01585 (♂) [MZ645137]
De. camelonota sp. nov. Banpo, Yixiang, Simao, Pu’er, Yunnan, China 25.x.2012 #01607 (♂) [MZ645138], #01608 (♀) [MZ645139]
De. paranigrovittata sp. nov. Baihualing, Longyang, Baoshan, Yunnan, China 3.viii.2012 #01145 (♂) [MZ645116]
From rearings of host infructescences collected from Baihualing, Baoshan, Yunnan, China 23.ix.2012 #01579 (♂) [MZ645131]
De. nigrovittata (Malloch, 1924) Dinghushan Nature Reserve, Zhaoqing, Guangdong, China (by net sweeping above herbs) 13.iv.2008 #00132 (♂) [MZ645104], #00135–137 (3♀) MZ645105–107]
23–26.iii.2009 #01582 (♀) [MZ645134], #01583 (♂) [MZ645135]
From rearings of infructescences of Rhaphidophora decursiva collected from Baihualing, Baoshan, Yunnan, China 5.ix.2012 #01177 (♀) [MZ645123], #01178 (♂) [MZ645124], #01179 (♂) [MZ645125], #01180 (♀) [MZ645126], #01182–184 (3♀) [MZ645127–129]
23.ix.2012 #01578 (♀) [MZ645130], #01580 (♂) [MZ645132], #01581 (♀) [MZ645133], #01721 (♀) [MZ645141]
Haoping Station, Taibaishan National Nature Reserve, Shaanxi, China (by net sweeping above herbs along waterside) 16.viii.2013 #01680 [MZ645140]

The examined specimens are deposited in the following institutes:

KIZ Kunming Natural History Museum of Zoology, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, China;

SEHU Systematic Entomology, the Hokkaido University Museum, Hokkaido University, Sapporo, Japan.

Species delimitation and description

As pointed out by Okada (1982) and Bock (1982), it is difficult to definitely determine the generic assignment of the studied specimens to Dettopsomyia Lamb, 1914 or Styloptera Duda, 1924, based on morphological characters, for the present. As we address this issue in Discussion, it needs a systematic revision for these genera based on a full-scale molecular phylogenetic analysis of the subfamily Drosophilinae and ancestral state reconstruction of the morphology by character-mapping on the inferred tree. In the present study, therefore, we provisionally classify all studied specimens into Dettopsomyia according to the principle of priority (ICZN), since there is a possibility that the two genera are synonymized in future systematic studies. Then, they were classified into morpho-species referring to Okada’s (1982) 13 characters (Table 1): the character states (referred to as CS-code in descriptions of species) for all the known and putatively new species of Dettopsomyia are summarized in Table 3. The morpho-species were further examined for other external morphology and detailed structures of dissected phallic and periphallic organs by the same methods as in Li et al. (2014). For each morpho-species, at least one representative specimen was selected for mitochondrial COI DNA sequencing. We followed Li et al. (2014) and Yang et al. (2017) for extraction of DNA, PCR and sequencing, using Folmer et al. (1994) primer pair LCO1490 (5’- GGTCAACAAATCATAAAGATATTGG -3’) and HCO2198 (5’- TAAACTTCAGGGTGACCAAAAAATCA -3’). The sequences were edited in the SeqMan module of the DNAStar package (DNAStar Inc. 1996), and aligned in MEGA7 (Kumar et al. 2016). We performed tree- and distance-based DNA barcoding, with a neighbor-joining (NJ) tree constructed in MEGA7 with K2P distances (i.e., the Kimura 2-parameter distances) and comparison of the maximum intraspecific and the minimum interspecific p-distances. The morpho-species were then reconsidered by integrating information from the morphology and DNA barcode data.

McAlpine (1981) was followed for the morphological terminology, and Zhang and Toda (1992) for the definitions of measurements and indices.

Table 3.

A character-state matrix of Okada’s (1982) 13 characters for all Dettopsomyia species.

Species Characters Reference*
1 2 3 4 5 6 7 8 9 10 11 12 13
De. formosa Lamb, 1914 A B C D E F G H i J K l M 1)
De. jacobsoni Duda, 1926 A B C D E F G H I J K L M 1)
De. preciosa (de Meijere, 1911) A B C D e f G H I J K L m 1)
De. fruhstorferi (Duda, 1924) f G i J k 1)
De. pictipes (de Meijere, 1911) A B C D e f G H I J k L m 1)
De. repletoides (Carson & Okada, 1980) a b c d E f G H i J k L m 1)
De. alba Carson & Okada, 1982 a b c d E f G H i j k L m 1)
De. acrostichalis Duda, 1926 G h I k 1)
De. nigrovittata (Malloch, 1924) a b c d E F G h i J k l M 1)
De. philippina Takada, 1976 a b C d E f g h i J k l m 1)
De. equscauda Takada & Momma, 1975 A b c d e f G H i J k L m 1)
De. bombax (Burla, 1954) C D E f G h i j k l m 1)
De. woodruffi Takada, 1990 A b D E G h i J k l M 2)
De. acutipenis sp. nov. A b ? ? e f G H i J k l M 3)
De. serripenis sp. nov. A b C D ? ? G H i J K ? M 3)
De. discontinua sp. nov. A b C D ? F G H i J K L M 3)
De. camelonota sp. nov. A B C D ? F G h i J K ? m 3)
De. paranigrovittata sp. nov. a b c D ? f g h i J k l M 3)

Results

Species delimitation

The specimens were assigned into six morpho-species (one known and five new) of the genus Dettopsomyia. The alignment of the 38 barcodes spans (658 nucleotide sites in length) included 169 variable sites, among which 156 were parsimony informative. Fig. 1 shows the NJ tree built with the barcodes (GenBank accession numbers: MZ645104MZ645141). The tree lends strong supports to the monophyly of each of the morpho-species with BP (bootstrap percentage) = 100, except De. serripenis sp. nov. for which only one barcode was determined. The minimum and maximum K2P distances between and within the morpho-species are shown in Table 4. All the minimum interspecific K2P distances (≥ 0.0924), except for that between De. serripenis sp. nov. and De. discontinua sp. nov. (0.0132), were substantially larger than the maximum intraspecific distances (≤0.0391). Dettopsomyia serripenis sp. nov. formed a highly supported clade (BP = 100) with a compact cluster (K2P ≤ 0.0048, BP = 100) of 12 barcodes of De. discontinua sp. nov. (Fig. 1, Table 4). However, the former is readily distinguished from the latter in the morphology of both male and female (see the morphological diagnosis defined below for De. discontinua sp. nov.). On the other hand, the largest intraspecific distance (0.0391) was observed within the morpho-species De. nigrovittata (Table 4). Although the 18 barcode sequences of this species formed a monophyletic cluster (BP = 100), they were split into two subclusters with BPs = 58 and 96 (Fig. 1). However, no significant differentiation attributable to this subdivision was detected in either morphology (see Taxonomic account), habitat or geographical distribution (Table 2) between the two subclusters. We therefore regarded all these 18 specimens as of the same species (i.e., De. nigrovittata). Similarly, we identified two specimens of which K2P distance (0.0152) slightly exceeded the least interspecific distance (0.0132) (Table 4) as De. paranigrovittata sp. nov. based on the morphology.

Figure 1. 

An un-rooted, neighbor-joining tree built with DNA barcodes (mitochondrial COI sequences) of six Dettopsomyia species. Label of each operational taxonomic unit (OTU) is given in the format of “voucher number (sex)”. Node confidences (i.e., bootstrap percentages from 1000 replicates) ≥ 50% are shown.

Table 4.

Minimum and maximum of intra- and interspecific K2P distances of six Dettopsomyia species.

Species n a Intraspecific distance Interspecific distancesb
Minimum Maximum 1 2 3 4 5 6
De. nigrovittata (Malloch, 1924) 18 0.0000 0.0391 0.1355 0.1330 0.1499 0.1380 0.1420
De. paranigrovittata sp. nov. 2 0.0152 0.0152 0.1741 0.1784 0.1946 0.1776 0.1708
De. camelonota sp. nov. 2 0.0000 0.0000 0.1621 0.1897 0.1435 0.1372 0.1320
De. acutipenis sp. nov. 3 0.0000 0.0017 0.1829 0.2069 0.1489 0.0978 0.0924
De. serripenis sp. nov. 1 n/a n/a 0.1484 0.1780 0.1445 0.1046 0.0132
De. discontinua sp. nov. 12 0.0000 0.0048 0.1756 0.1847 0.1434 0.1035 0.0164

Taxonomic account

Dettopsomyia Lamb, 1914

Dettopsomyia Lamb, 1914: 349; Wheeler & Takada 1964: 210; Bock 1982: 42; Okada 1982: 270; Bächli et al. 2004: 119. Type species: Dettopsomyia formosa Lamb, 1914.

Pictostyloptera Duda, 1924: 192. Syn. Duda 1926: 61. Type species: Drosophila preciosa de Meijere, 1911.

Included species

acrostichalis Duda, 1926; alba Carson & Okada in Okada (1982); bombax (Burla, 1954); equscauda Takada & Momma, 1975; formosa Lamb, 1914; fruhstorferi (Duda, 1924); jacobsoni Duda,1926; nigrovittata (Malloch, 1924); philippina Takada, 1976; pictipes (de Meijere, 1911); preciosa (de Meijere, 1911); repletoides (Carson & Okada, 1980); woodruffi Takada in Takada et al. (1990); acutipenis Wang & Gao, sp. nov.; camelonota Wang, Li & Gao sp. nov.; discontinua Wang & Gao, sp. nov.; paranigrovittata Wang, Li & Gao, sp. nov.; and serripenis Wang & Gao, sp. nov.

Geographical distribution

Collection records of all the known species from the world are plotted in a map (Fig. 2) using Simplemappr (http://www.simplemappr.net/), and collection sites of the five new species plotted in a separate, online map (Fig. 3) from https://d-maps.com.

Figure 2. 

Geographical distribution of the known species in the genus Dettopsomyia.

Figure 3. 

Geographical distribution of five newly described species in the genus Dettopsomyia.

Key to Oriental species of Dettopsomyia

In this key, some figures published by Lamb (1914), Duda (1924, 1926), Okada (1956, 1982), Hardy (1965), and Takada (1976) are cited.

1 Wing spotted (Figs 5C, 6C, 7C; Lamb 1914: fig. 33; Duda 1924: fig. 39; Duda 1926: fig. 3; Hardy 1965: fig. 20b). 2
Wing not spotted (Figs 4C, 8C; Duda 1924: fig. 40). 7
2 Acrostichal bristles present (Okada 1982: fig. 1B, C). 3
Acrostichal bristles absent (Figs 57B; Okada 1982: fig. 1A). 4
3 Wing with two black spots along costa (Duda 1924: fig. 39). De. preciosa (de Meijere)
Wing with four black spots along costa (Duda 1926: fig. 3). De . jacobsoni Duda
4 Wing with approximately 24 pale spots; R4+5 and M1 parallel (Fig. 7C). De. camelonota Wang, Li & Gao, sp. nov.
Wing with 14–17 pale spots; R4+5 and M1 divergent distally (Figs 5C, 6C; Lamb 1914: fig. 33; Hardy 1965: fig. 20b). 5
5 Ocellar setae inserted inside triangle made by ocelli (Okada 1982) fig. 1A); epandrial, ventral lobe elongated (Okada 1982: fig. 2A). De. formosa Lamb
Ocellar setae inserted outside triangle made by ocelli (Figs 5B, 6B); epandrial, ventral lobe short (Fig. 5F, G) or absent (Fig. 6F, G). 6
6 Cercus somewhat pointed but not protruded caudoventrally (Fig. 5F); surstylus with 14 or 15 prensisetae arranged in V-shape (Fig. 5F, G); marginal peg-like ovisensilla in continuous row (Fig. 5J, K). De. serripenis Wang & Gao, sp. nov.
Cercus caudoventrally protruded ventrad like finger (Fig. 6F); surstylus with approximately 11 prensisetae on distal margin and 9 or 10 ones on medial portion of outer surface, arranged together nearly in circle (Fig. 6F, G); row of marginal peg-like ovisensilla interrupted around subterminal, long, trichoid seta (Fig. 6J, K). De. discontinua Wang & Gao, sp. nov.
7 R2+3 nearly straight (Fig. 8C; Takada 1976: fig. 1c). 8
R2+3 more or less curved to costa apically (Fig. 4C). 9
8 Scutum and scutellum blackish brown to black (Fig. 8B). De. paranigrovittata Wang, Li & Gao, sp. nov.
Scutum and scutellum with brownish, longitudinal stripes (Takada 1976: fig. 1a). De. philippina Takada
9 Acrostichal bristles present. 10
Acrostichal bristles absent (Figs 4B, 8B). 11
10 R4+5 and M1 divergent distally (Duda 1924: fig. 40). De. pictipes (de Meijere)
R4+5 and M1 parallel De. acrosticholis Duda
11 C-index < 1.0 (Okada 1956: fig. 31). De. nigrovittata (Malloch)
C-index > 1.0 (Fig. 4A). 12
12 Scutum with 10 dark stripes De. fruhstorferi (Duda)
Scutum with < 10 dark stripes (Fig. 4B), or with complex dark marks. 13
13 Acrostichal setulae in 2 rows. De. equscauda Takada & Momma
Acrostichal setulae in 4 rows (Fig. 4B). De. acutipenis Wang & Gao, sp. nov.

Descriptions of species

Dettopsomyia acutipenis Wang & Gao, sp. nov.

Figure 4

Material

Holotype ♂ (#00151), Yunnan: Xishuangbanna Tropical Botanical Garden, the Chinese Academy of Sciences, Menglun, Mengla, Xishuangbanna, ca. 570 m (21.92°N, 101.28°E), 19.iii.2006, ex flower of Zinger sp. (M.J. Toda) (KIZ). Paratypes China: 7♀ (#00380–386), the data same as holotype except for 18.vi.2007 (J.J. Gao); 3♀ (#00387–389), the data same as holotype except for 16.vi.2007 (J.J. Gao) (KIZ).

Diagnosis

This species differs in CS-code (Ab??efGHiJklM) from all the remaining congeneric species, except for De. fruhstorferi (?????fG?iJk?? according to Okada, 1982), which is, however, distinguished from the new species by the number of dark, longitudinal stripes on scutum: six in the new species, but ten in De. fruhstorferi.

Description

(♂, ♀). Head (Fig. 4A, B): Eye red, much oblique to body axis, with dense interfacetal setulae. Ocellar triangle matte black. Ocellar setae located outside triangle made by ocelli. Fronto-orbital plate anteriorly with a black spot at the base of proclinate and anterior reclinate orbital setae. Frons grayish yellow, with pale brown stripes. Face yellow; carina large, ventrally with blackish brown, T-shaped spot. Clypeus black. Gena yellowish brown, with dark stripe along ventral margin. Palpus yellow. Pedicel (2nd antennal segment) yellow, laterally with black spot; 1st flagellomere (3rd antennal segment) grayish yellow.

Thorax (Fig. 4A, B): Scutum, scutellum, and thoracic pleura yellowish brown; scutellum apically white. Scutum with six blackish brown stripes; median pair close to each other. Scutellum medially with X-shaped, dark marking posteriorly covering the bases of apical scutellar setae, laterally with dark spots at the bases of basal scutellar setae. Thoracic pleura with three blackish, longitudinal stripes. Acrostichal long setae absent; acrostichal setulae in four rows. Dorsocentral setae three pairs. Basal scutellar setae slightly divergent; apical scutellar setae cruciate.

Figure 4. 

Dettopsomyia acutipenis Wang & Gao, sp. nov. (A–I #00151, J–L paratype #00380) A left lateral habitus B head and thorax (dorsal view) C wing (right, dorsal view) D abdomen (lateral view) E abdomen (dorsal view) F periphallic organs (posterolateral view) G surstylus H phallic organs (ventral view) I aedeagus (dorsolateral view) J oviscapt (lateral view) K oviscapt (ventral view) L spermatheca. Abbreviations: aed = aedeagus, aed apod = aedeagal apodeme, cerc = cercus, epand = epandrium, hypd = hypandrium, sur = surstylus. Scale bars: 1.0 mm (photograph) or 0.1 mm (line drawing).

Wing (Fig. 4C): Wing pale yellow. Veins yellowish brown. Costal lappet black, moderate in size. R2+3 curved to costa apically; R4+5 and M1 slightly diverged from each other distally. Haltere pale yellow, ventrally with small grayish patch; stalk slightly grayish.

Legs (Fig. 4A): Legs yellow: femora and tibiae ringed.

Abdomen (Fig. 4D, E): Tergites yellow, posteriorly with narrow, blackish brown, dorsomedially interrupted bands, which bend forward laterally, and with an isolated black spot on lateral margin.

Male terminalia (Fig. 4F–I): Epandrium pubescent except for anterior margin and ventral portion, with five setae per side on ventral portion and triangular, distally somewhat roundish apodeme on antero-dorsal to -sublateral margin, slightly protruded anteriad at anteroventral corner. Surstylus broadly fused to epandrium; distal margin with a row of 12 or 13 peg-like, apically pointed prensisetae, which are more loosely arranged dorsally; outer surface with six or seven long, trichoid setae on subdorsal to ventral portion; caudoventral apex with a few short, trichoid setae. Cercus oblong, wider than 1/2 length, partially fused to epandrium, caudoventrally pointed, pubescent except for anteroventral margin, with approximately 17 setae. Hypandrium somewhat triangular, with a pair of minute setae (paramedian setae?), caudomedially deeply notched and revolute along inner edges, with large patches of pubescence on the revolute parts. Aedeagus apically acute, slightly curved dorsad, basally with recurved, dorsal flap; aedeagal guide broadly fused to revolute portion of hypandrium; apodeme fused to aedeagus, rod-like, < 1/3 length of aedeagus.

Female terminalia (Fig. 4J–L): Oviscapt with single lateral and 13 or 14 marginal, apically more or less pointed, peg-like ovisensilla, and one subterminal, trichoid seta; anteroventral bridge short. Spermatheca somewhat fusiform, basally ridged; introvert ca. 1/4 height of outer capsule.

Measurements : BL (straight distance from anterior edge of pedicel to tip of abdomen) = 1.69 mm in holotype (range in 9♀ paratypes: 1.42–2.18 mm); ThL (distance from anterior notal margin to apex of scutellum) = 0.71 (0.62–0.74) mm; WL (distance from humeral cross vein to wing apex) = 1.46 (1.40–1.60) mm; WW (maximum wing width) = 0.73 (0.67–0.86) mm.

Indices : arb (dorsal branches/ventral branches of arista) = 3/2 in holotype (range in 9♀, or less if noted, paratypes: 3–4/2), FW/HW (frontal width/head width) = 0.59 (0.57–0.61), ch/o (maximum width of gena/maximum diameter of eye) = 0.42 (0.41–0.51), prorb (proclinate orbital seta/posterior reclinate orbital seta in length) = 0.70 (0.53–0.70), rcorb (anterior reclinate orbital seta/posterior reclinate orbital seta in length) = 0.33 (0.32–0.47), vb (subvibrissal seta/vibrissa in length) = 0.44 (0.24–0.47), dc1l (1st dorsocentral seta/3rd dorsocentral seta in length) = 0.91 (0.88–0.95), dc2l (2nd dorsocentral seta/3rd dorsocentral seta in length) = 0.78 (0.77–0.92), sctl (basal scutellar seta/apical scutellar seta in length) = (n/a)/(0.96–1.06), sterno (anterior katepisternal seta/posterior katepisternal seta in length) = 0.39 (0.39–0.56), orbito (distance between proclinate and posterior reclinate orbital setae/distance between inner vertical and posterior reclinate orbital setae) = 0.56 (0.40–0.61), dc1p (distance between ipsilateral 1st and 2nd dorsocentral setae/distance between 2nd dorsocentral setae) = 0.76 (0.70–0.79), dc2p (distance between ipsilateral 2nd and 3rd dorsocentral setae/distance between 2nd dorsocentral setae) = 0.79 (0.69–0.80), sctlp (distance between ipsilateral scutellar setae/distance between apical scutellar setae) = 0.94 (0.93–1.04), C (2nd costal section between subcostal break and R2+3/3rd costal section between R2+3 and R4+5) = 1.31 (1.17–1.51), 4c (3rd costal section between R2+3 and R4+5/M1 between r-m and dm-cu) = 2.29 (1.72–2.54), 4v (M1 between dm-cu and wing margin/M1 between r-m and dm-cu) = 3.21 (2.40–3.36), 5× (CuA1 between dm-cu and wing margin/dm-cu between M1 and CuA1) = 3.82 (2.97–3.85), ac (3rd costal section between R2+3 and R4+5/distance between distal ends of R4+5 and M1) = 2.92 (2.84–3.33), M (CuA1 between dm-cu and wing margin/M1 between r-m and dm-cu) = 1.43 (1.10–1.48), C3F (length of heavy setation in 3rd costal section/length of 3rd costal section) = 0.53 (0.50–0.60).

Distribution

China (Yunnan).

Relationships

This species closely resembles De. repletoides (CS-code = abcdEfGHiJkLm, Okada 1982) in the structures of male terminalia Carson and Okada 1980: fig. 3).

Etymology

Referring to the apically more or less acute (acuti-) aedeagus (penis).

Dettopsomyia serripenis Wang & Gao, sp. nov.

Figure 5

Material

Holotype : ♂ (#00152), Xishuangbanna Tropical Botanical Garden, the Chinese Academy of Sciences, Menglun, Mengla, Xishuangbanna, Yunnan, China, ca. 570 m (21.92°N, 101.28°E), 19.iii.2006, ex Zingerberaceae flower (M.J. Toda) (KIZ). Paratypes: China: 1♂ (#00153), same data except for 24.iii.2006, ex Alocasia odora; 1♀ (#00154), same data except for 25.iii.2006; 2♂, 2♀ (#00155–158), same data except for habitat (host plant unknown) (M.J. Toda) (KIZ, SEHU).

Diagnosis

This species is characteristic in sharing the spotted wings (Fig. 5C) with three known species of Dettopsomyia, De. formosa (Lamb 1914: fig. 33; Hardy 1965: fig. 20b), De. jacobsoni (Duda 1926: fig. 3) and De. preciosa (de Meijere 1911: fig. 49; Duda 1924: fig. 39), but differs in CS-code (AbCD??GHiJK?M) from them: De. formosa (ABCDEFGHiJKlM), De. jacobsoni (ABCDEFGHIJKLM) and De. preciosa (ABCDefGHIJKLm) (Table 3).

Description

(♂, ♀; not repeating characters common to De. acutipenis sp. nov.). Head (Fig. 5A, B): Ocellar setae located just outside triangle made by ocelli. Frons yellow, with blackish brown stripes. Face gray. First flagellomere black.

Figure 5. 

Dettopsomyia serripenis Wang & Gao, sp. nov. (A–I #00152, J–L paratype #00156) A left lateral habitus B head and thorax (dorsal view) C wing (right, dorsal view) D abdomen (lateral view) E abdomen (dorsal view) F periphallic organs (posterolateral view) G surstylus H phallic organs (ventral view) I phallic organs (dorsolateral view) J oviscapt (lateral view) K oviscapt (ventral view) L spermatheca. Scale bars: 1.0 mm (photograph) or 0.1 mm (line drawing).

Thorax (Fig. 5A, B): Scutum, scutellum, and thoracic pleura yellow. Scutum with confluent stripes. Scutellum with somewhat H-shaped, dark marking medially and dark stripes covering bases of ipsilateral scutellar setae laterally. Acrostichal setulae in 2–4 vestigial rows. Dorsocentral setae two pairs.

Wing (Fig. 5C) grayish yellow, black to blackish brown basally, with four dark spots along anterior margin and 14 scattered, pale spots. Veins brown. R2+3 waved, strongly curved to costa apically; R4+5 and M1 distally diverged from each other.

Legs (Fig. 5A) pale brown.

Abdomen (Fig. 5D, E): Tergites blackish brown, laterally with yellowish spots: one per side on tergite II, two per side on tergites III–VI.

Male terminalia (Fig. 5F–I): Epandrium with three setae per side laterally; ventral lobe short, narrow, apically round and sclerotized like peg, with two small setae subapically. Surstylus with prensisetae arranged in V-shape (approximately seven on caudal margin and 6–8 in oblique row on outer surface; one or two dorsalmost on outer surface somewhat separated from others), several upward-curved setae on ventral to subventral portion of inner surface and one or two trichoid setae on outer surface near base of epandrial ventral lobe. Cercus broadly fused to epandrium, pubescent anteriorly, with approximately 28 setae; several setae along caudoventral margin shorter. Hypandrium somewhat trapezoid; apodeme anteriorly truncate, twice as wide as long. Paramere fused to hypandrium, not pubescent but with a single setula. Aedeagus distally membranous, subapically dilated and serrated on lateral margins around gonopore, apically sharply pointed; apodeme as long as aedeagus.

Female terminalia (Fig. 5J–L): Oviscapt with one trichoid and two peg-like lateral ovisensilla and 15 marginal peg-like ovisensilla more loosely arranged anteriorly; distal portion approximately 1/4 of whole length, convex on dorsal margin in lateral view. Spermathecal capsule as broad as long, finely wrinkled on basal half, with shallow apical indentation; introvert ca. 4/5 height of outer capsule.

Measurements : BL = 1.51 mm in holotype (range in 3♂ paratypes: 1.41–1.66 mm; range in 3♀ paratype: 1.53–1.80 mm); ThL = 0.57 (0.57; 0.58–0.62) mm; WL = 1.37 (1.34–1.41; 1.47–1.52) mm; WW = 0.73 (0.66–0.71; 0.71–0.74) mm.

Indices : arb = 3/2 (range in 3♂, 3♀, or less if noted, paratypes: 3 or 4/2), FW/HW = 0.60 (0.59–0.62), ch/o = 0.38 (0.33–0.47), prorb = 0.60 (0.49–0.70), rcorb = 0.20 (0.20–0.23), vb = 0.35 (0.34–0.67), dcl (anterior dorsocentral seta/posterior dorsocentral seta in length) = 0.74 (0.82–0.89), sctl = (n/a)/(1♂: 0.90), sterno = 0.71 (0.44–0.68), orbito = 0.29 (0.21–0.26), dcp (distance between ipsilateral dorsocentral setae/distance between anterior dorsocentral setae) = 0.71 (0.65–0.81), sctlp = 1.27 (1.03), C = 1.00 (0.89–1.16), 4c = 2.51 (1.71–2.79), 4v = 2.24 (1.79–2.82), 5× = 1.90 (1.68–2.01), ac = 2.78 (2.13–3.05), M = 0.87 (0.84–1.10), C3F = 0.52 (0.54–0.69).

Distribution

China (Yunnan).

Etymology

Referring to the serrated, lateral margins of the gonopore of the aedeagus.

Dettopsomyia discontinua Wang & Gao, sp. nov.

Figure 6

Material

Holotype : ♂ (#01585), Banpo, Yixiang, Simao, Pu’er, Yunnan, China, ca. 1300 m (22°44'N, 101°.07'E), by net sweeping above herbs, 2.x.2012 (J.J. Gao) (KIZ). Paratypes: China: 1♂ (#01584), same data as holotype; 5♂, 1♀ (#01139–1144), Zaotanghe, Baihualing, Baoshan, Yunnan, ca. 1540 m (25°18'N, 98°47'E), 4.viii.2012, ex small mushroom (J.J. Gao); 3♀, 3♂ (#01167–1169, #01172–1174), from decaying aroid (Rhaphidophora decursiva) infructescences collected from Baihualing, Baoshan, Yunnan, 23.ix.2012 (J.J. Gao, Z. Fu, and J.M. Chen) (KIZ, SEHU).

Diagnosis

This species is closely related to De. serripenis sp. nov., forming a highly supported (BP = 100) clade with it (Fig. 1). These two species are indistinguishable in CS-code from each other: De. discontinua sp. nov. (AbCD?FGHiJKLM) and De. serripenis sp. nov. (AbCD??GHiJK?M). However, they can be easily distinguished from each other by the following characters: 1) cercus caudoventrally strongly sclerotized and protruded ventrad like finger (Fig. 6F) in De. discontinua sp. nov. (abbreviated Dd here), but only pointed at caudoventral corner (Fig. 5F) in De. serripenis sp. nov. (abbreviated Ds); 2) surstylus with approximately 11 prensisetae on distal margin and nine or ten ones on medial portion of outer surface, arranged together nearly in circle (Fig. 6F, G) in Dd, but with 14 or 15 prensisetae arranged in V-shape (Fig. 5F, G) in Ds; and 3) marginal peg-like ovisensilla in row interrupted around subterminal, long, trichoid seta (Fig. 6J, K) in Dd, but in continuous row (Fig. 5J, K) in Ds.

Figure 6. 

Dettopsomyia discontinua Wang & Gao, sp. nov. (A–I #01585, J–L paratype #01168) A left lateral habitus B head and thorax (dorsal view) C wing (right, dorsal view) D abdomen (lateral view) E abdomen (dorsal view) F periphallic organs (posterolateral view) G surstylus H phallic organs (ventral view) I phallic organs (dorsolateral view) J oviscapt (lateral view) K oviscapt (ventral view) L spermatheca. Scale bars: 1.0 mm (photograph) or 0.1 mm (line drawing).

Description

(♂, ♀; not repeating characters common to De. serripenis sp. nov.). Head (Fig. 6A, B): Frons with black stripes. Gena yellow. Palpus grayish yellow.

Thorax (Fig. 6A, B): Scutum, scutellum, and thoracic pleura with color patterns similar to those of De. serripenis sp. nov. Acrostichal setulae in two rows. Basal scutellar setae slightly converged.

Wing (Fig. 6C): Wing maculated as in De. serripenis sp. nov.

Legs (Fig. 6A) pale grayish yellow.

Abdomen (Fig. 6D, E): Tergites blackish brown to black; II–V each laterally with a pale brown spot per side.

Male terminalia (Fig. 6F–I): Epandrium pubescent on mediolateral portion only, with one seta per side on mediolateral portion; ventral lobe not differentiated; apodeme narrow, somewhat triangular. Surstylus somewhat quadrate, large plate, with one trichoid seta and 10–11 prensisetae in sinuated row on outer surface and 6–8 prensisetae decreasing in size downward on caudal margin. Cercus unpubescent, with approximately 33 setae. Hypandrium somewhat hemicircular; apodeme slightly wider than long. Aedeagus subapically with a pair of triangular lateral flaps; apodeme shorter than aedeagus.

Female terminalia (Fig. 6J–L): Oviscapt with three trichoid lateral ovisensilla, 14–16 peg-like marginal ovisensilla and one subterminal, trichoid, long seta; distal portion approximately 1/3 of whole length, nearly flat on dorsal margin in lateral view.

Measurements : BL = 1.50 mm in holotype (range in 5♂ paratypes: 1.42–1.67 mm; range in 4♀ paratypes: 1.57–1.75 mm); ThL = 0.52 (0.55–0.64; 0.55–0.68) mm; WL = 1.30 (1.26–1.37; 1.36–1.58) mm; WW = 0.66 (0.62–0.70; 0.63–0.80) mm.

Indices : arb = 4 or 5/2 (range in 5♂, 4♀, or less if noted, paratypes: 4/2), FW/HW = 0.60 (0.57–0.61), ch/o = 0.38 (0.35–0.49), prorb = 0.72 (0.59–0.77), rcorb = 0.14 (0.16–0.21), vb = 0.32 (0.22–0.46), dcl = 0.74 (0.72–0.85), sctl = 0.98 (0.95–1.12), sterno = 0.73 (0.44–0.64), orbito = 0.19 (0.25–0.32), dcp = 0.65 (0.65–1.08), sctlp = 1.06 (0.95–1.14), C = 0.88 (0.90–0.96), 4c = 2.53 (2.11–2.34), 4v = 2.39 (1.93–2.30), 5× = 2.04 (1.63–2.09), ac = 3.18 (2.68–3.06), M = 0.93 (0.78–0.85), C3F = 0.58 (0.42–0.63).

Distribution

China (Yunnan).

Etymology

Referring to the interruptedly arranged marginal ovisensilla.

Dettopsomyia camelonota Wang, Li & Gao, sp. nov.

Figure 7

Material

Holotype : ♂ (#01607), Banpo, Yixiang, Simao, Pu’er, Yunnan, China, ca. 1300 m (22.73°N, 101.12°E), 25.x.2012 (J.J. Gao) (KIZ). Paratype: China: 1♀ (#01608), same data as holotype (KIZ).

Diagnosis

This species differs from all the remaining congeneric species in CS-code (ABCD?FGhiJK?m) (Table 3) and having the following diagnostic characters: unique, distinctly humpbacked scutum in lateral view (Fig. 7A); aedeagus characterized by large, vault-like arch (Fig. 7H, I); and large, spoon-shaped paramere densely hirsute on inner surface (Fig. 7H, I). It resembles De. formosa, De. jacobsoni, De. serripenis sp. nov., and De. discontinua sp. nov. in wing marking pattern, but can be distinguished from them by much more (approximately 24) pale spots (Fig. 7C).

Figure 7. 

Dettopsomyia camelonota Wang, Li & Gao, sp. nov. (A–I #01607, J–L paratype #01608) A left lateral habitus B head and thorax (dorsal view) C wing (right, dorsal view) D abdomen (lateral view) E abdomen (dorsal view) F periphallic organs (posterolateral view) G surstylus H phallic organs (ventral view) I phallic organs (dorsolateral view) J oviscapt (lateral view) K oviscapt (ventral view) L spermatheca. Scale bars: 1.0 mm (photograph) or 0.1 mm (line drawing).

Description

(♂, ♀; not repeating characters common to De. acutipenis sp. nov.). Head (Fig. 7A, B): Ocellar setae located just inside triangle made by ocelli. Frons with blackish brown stripes. Face grayish yellow to blackish brown; carina broad, dorsally strongly swollen and blackish brown, medially yellowish brown, ventrally nearly flat, black and with broad, pale yellow, traverse band. Clypeus blackish yellow. Gena pale yellow, ventrally black. Palpus gray, paddle-shaped in ventral view, with one prominent apical seta and several ventral ones. Antennal pedicel long triangular, black, laterally with yellowish patch; 1st flagellomere long, somewhat triangular, black, with pale patch on inner, dorsal margin; arista with brown dorsal and ventral branches nearly as long as whitish trunk.

Thorax (Fig. 7A, B): Scutum, scutellum, and thoracic pleura grayish yellow. Scutum with blackish brown to black, longitudinal stripes interweaved with each other. Scutellum medially with blackish brown to black patch merged with lateral black spots covering bases of ipsilateral scutellar setae. Acrostichal setulae in two vestigial rows. Dorsocentral setae three pairs; anteriormost pair distinctly shorter and thinner, located slightly anterior to transverse suture and more widely separated from each other. Basal scutellar setae divergent.

Wing (Fig. 7C): Veins brown. R2+3 not waved medially, strongly curved to costa apically. R4+5 and M1 veins distally nearly parallel with each other.

Legs (Fig. 7A) yellow to pale brown.

Abdomen (Fig. 7D, E): Tergites blackish brown.

Male terminalia (Fig. 7F–I): Epandrium nearly completely smooth, with two setae per side on ventral portion; ventral lobe very small; somewhat triangular apodeme present on anteromedial margin. Surstylus with a row of approximately six prensisetae on distal margin, approximately four thick, short setae on submedial to ventral portion of outer surface and a few trichoid setae around caudoventral corner. Cercus broadly fused to epandrium, large, somewhat fan-shaped, caudoventrally not pointed, nearly smooth, with approximately 25 short setae. Hypandrium broad, anteriorly rounded, with triangular apodeme. Aedeagus bilobed; apodeme approximately 1/2 as long as aedeagus.

Female terminalia (Fig. 7J–L): Oviscapt with three lateral trichoid and 12 or 13 marginal, apically somewhat blunt peg-like ovisensilla. Spermathecal capsule spherical, strongly constricted near base; introvert ca. 3/5 height of outer capsule.

Measurements : BL = 1.54 mm in holotype (1♀ paratype: 1.70 mm); ThL = 0.57 (0.65) mm; WL = 1.42 (1.53) mm; WW = 0.72 (0.72) mm.

Indices : arb = 4/2 (1♀: 4/2), FW/HW = 0.65 (0.64), ch/o = 0.41 (0.48), prorb = 0.71 (n/a), rcorb = 0.18 (0.15), vb = 0.34 (0.29), dc1l = 0.36 (0.28), dc2l = n/a (0.72), sctl = 0.94 (0.95), sterno = n/a (0.80), orbito = 0.18 (0.21), dc1p = 0.39 (0.32), dc2p = 0.67 (0.62), sctlp = 1.14 (1.00), C = 0.94 (0.90), 4c = 2.75 (2.60), 4v = 3.00 (2.73), 5× = 1.85 (1.63), ac = 4.21 (4.17), M = 1.04 (0.87), C3F = 0.34 (0.50).

Distribution

China (Yunnan).

Etymology

A combination of the Greek words camelos and notos, referring to the humped, camel-like notum.

Dettopsomyia paranigrovittata Wang, Li & Gao, sp. nov.

Figure 8

Materials

Holotype : ♂ (#01145), ex. inflorescence of Rh. decursiva, Laomengzhai, Baihualing, Baoshan, Yunnan, China, ca. 1500 m (25°17'N, 98°48'E), 3.viii.2012 (J.J. Gao) (KIZ). Paratype: China: 1♂ (#01579), emerged (together with many adults of De. nigrovittata) from decaying spathes of Rh. decursiva collected from Laomengzhai, Baihualing, Baoshan, Yunnan (same as holotype) and cultured in laboratory, 23.ix.2012 (J.J. Gao, Z. Fu, J.M. Chen) (KIZ).

Diagnosis

This species closely resembles De. nigrovittata in the external morphology and male terminalia, but can be distinguished from it by the surstylus chaetotaxy: in De. paranigrovittata sp. nov., approximately 23 subequal, peg-like prensisetae arranged roughly in five sets on medial to distal portion of outer surface and two upward-curved, trichoid setae on subventral portion of inner surface (Fig. 8F, G); but in De. nigrovittata, approximately 25 more or less heteromorphic setae arranged in three rows on upper half of outer surface and two larger setae at lower tip (Okada 1956: fig. 31C, as De. argentifrons).

Figure 8. 

Dettopsomyia paranigrovittata Wang, Li & Gao, sp. nov. (A–I #01145) A left lateral habitus B head and thorax (dorsal view) C wing (right, dorsal view) D abdomen (lateral view) E abdomen (dorsal view) F periphallic organs (posterolateral view) G surstylus H phallic organs (ventral view) I phallic organs (ventrolateral view). Scale bars: 1.0 mm (photograph) or 0.1 mm (line drawing).

Description

(♂; not repeating characters common to De. acutipenis sp. nov.). Head (Fig. 8A, B): Eye nearly rectangular to body axis. Fronto-orbital plate yellowish brown. Frons and frontal vittae grayish brown, somewhat shining. Face grayish yellow, black at middle and lateral sides; carina grayish yellow, rather prominent. Gena blackish brown, with pale spots antero- and medio-dorsally. Palpus grayish yellow, with large black spot. Antennal pedicel grayish yellow; 1st flagellomere dark gray. Subvibrissal seta short.

Thorax (Fig. 8A, B): Scutum blackish brown to black, with four narrow, silver stripes; scutellum and thoracic pleura blackish brown. Acrostichal setulae in six rows. Dorsocentral setae two pairs. Basal scutellar setae divergent.

Wing (Fig. 8C) hyaline. Veins pale brown. R2+3 nearly straight; R4+5 and M1 distally parallel. Haltere pale whitish to grayish yellow.

Legs (Fig. 8A) pale brown to blackish brown.

Abdomen (Fig. 8D, E): Tergites entirely black.

Male terminalia (Fig. 8F–I): Epandrium pubescent on lateral to dorsal portion, with one and two setae per side on sub-dorsal and -ventral portions, respectively; ventral lobe distally with five long, trichoid setae; apodeme on anterior margin. Surstylus somewhat triangular, large plate. Cercus broadly fused to epandrium, somewhat roundish at caudoventral corner, entirely pubescent, with approximately 36 setae. Hypandrium anteriorly slightly narrower, caudomedially notched. Paramere fused to hypandrium, densely pubescent, apically with one minute setula. Aedeagus curved ventrad proximally but dorsad distally, distally narrowing like horn in lateral view, ventro-subapically with large, oval gonopore; apodeme slightly shorter than aedeagus.

Measurements : BL = 1.69 mm in holotype (1♂ paratype: 1.52 mm); ThL = 0.68 (0.65) mm; WL = 1.50 (1.40) mm; WW = 0.74 (0.71) mm.

Indices : arb = 4/2 (1♂ paratype: 4/2), FW/HW = 0.56 (0.55), ch/o = 0.36 (0.41), prorb = 0.68 (0.73), rcorb = n/a (0.32), dcl = 0.71 (0.71), sctl = 0.83/(0.85), sterno = n/a (0.61), orbito = 0.57 (0.52), dcp = 0.80 (0.83), sctlp = 0.91 (0.92), C = 1.36 (1.23), 4c = 1.94 (2.20), 4v = 2.92 (3.15), 5× = 3.20 (2.67), ac = 4.73 (3.89), M = 1.23 (1.25), C3F = 0.60 (0.65).

Distribution

China (Yunnan).

Etymology

Referring to the close morphological affinity to De. nigrovittata.

Discussion

Since the early days of taxonomy for Dettopsomyia and Styloptera, these two genera have been ambiguous in their systematic positions. Until now, only few phylogenetic studies have been conducted to clarify the relationships between them. Grimaldi (1990) classified these two genera with Jeannelopsis Seguy, Tambourella Wheeler, Mulgravea Bock, Sphaerogastrella Duda, Hypselothyrea de Meijere, and Liodrosophila Duda in the Styloptera genus group, based on a cladistic analysis using 217 characters of 120 species. However, each genus was represented by a single species in his analysis. In Yassin’s (2013) Bayesian phylogenetic tree based on DNA sequences of 70 genera of the Drosophilidae, Styloptera (represented by S. formosae only) was coupled with the subgenus Dorsilopha Sturtevant (represented by Drosophila busckii Coquillett, 1901), and Dettopsomyia (represented by De. nigrovittata) was placed into a clade containing the genera Jeannelopsis, Dichaetophora Duda, Hirtodrosophila Duda, Zygothrica Wiedemann, and Mycodrosophila Oldenberg. To completely solve this ambiguity in the systematics of the subfamily Drosophilidae a full-scale molecular phylogenetic analysis should be conducted with extensive taxon sampling from Dettopsomyia, Styloptera and putatively related genera and subgenera. The species diversity of Dettopsomyia and Styloptera has also been less explored: only 13 and ten species were known, respectively, before the present study. Our finding of five new Dettopsomyia species from southwestern China (Fig. 3) suggests that more unknown species remain to be discovered from the Oriental region. To precisely delimit the boundaries of these genera, as many species as possible need to be incorporated into the systematic study.

The natural history of Dettopsomyia flies is still less explored. However, our collection records suggest their florivorous nature. Adult flies of De. acutipenis sp. nov. and De. serripenis sp. nov. were collected from flowers of Zingerberaceae, De. serripenis sp. nov. also from inflorescences of Alocasia odora (Araceae), and De. paranigrovittata from an inflorescence of Rhaphidophora decursiva (Araceae). Additionally, offspring adults of De. paranigrovittata sp. nov., De. discontinua sp. nov., and De. nigrovittata emerged from infructescences with decayed spathe of R. decursiva in laboratory rearings, and Carson and Okada (1980) reported rearing De. repletoides (under the name of Styloptera repletoides) from infructescences of Colocasia esculenta (Araceae). Wheeler (1951) observed dipteran larvae and puparia in a rotting, bleeding part of banana plant, and adults emerged from them and were identified as De. nigrovittata. Thus, some species of Dettopsomyia use decayed plant materials as a breeding substrate.

Acknowledgements

This work was supported by the National Science Foundation of China (No. 32060112) to JJG and the fund of the Ministry of Science and Technology of China (Nos 2011FY120200 and 2012FY110800) to the SCDBC.

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