Revision of the Japanese species of Epicephala Meyrick with descriptions of seven new species (Lepidoptera, Gracillariidae)

Abstract Epicephala moths are involved in obligate mutualisms with their Phyllanthaceae hosts, in which the female moths assure pollination and, in return, their progeny develop by consuming the seeds. Ecological, molecular and geographical data suggest that the genus includes several hundred species, but the majority remains to be formally described. Here we revise the Japanese species of Epicephala Meyrick, 1880. In addition to two previously named species, seven species are newly described: Epicephala anthophilia sp. n., Epicephala lanceolatella sp. n., Epicephala perplexa sp. n., Epicephala obovatella sp. n., Epicephala corruptrix sp. n., Epicephala parasitica sp. n. and Epicephala nudilingua sp. n. The first four are species involved in obligate pollination mutualism, while the fifth is a pollinating seed parasite and the last two are derived non-pollinating seed parasites of herbaceous Phyllanthus. Each of the nine Japanese Epicephela species is specialized to a single plant species in the genera Glochidion, Breynia or Phyllanthus, except for Epicephala obovatella and Epicephala corruptrix that each utilizes two closely related Glochidion species. Considerable variations are found in pollination and oviposition behaviors among species, which are reflected in their proboscis and ovipositor morphologies, respectively. Molecular phylogeny indicated that there have been repeated transitions in oviposition mode during the diversification of Epicephala, which were accompanied by changes in ovipositor morphology, as suggested by a correlation analysis. Keys to species are provided.


Introduction
The genus Epicephala Meyrick, 1880 (Gracillariidae) has recently become an important taxon in ecology and evolutionary biology because of their mutualisms with plants in the genera Glochidion, Breynia and Phyllanthus (Phyllanthaceae) (Kato et al. 2003;Kawakita and Kato 2009;Kawakita 2010). The females of Epicephala possess specialized sensilla-bearing proboscises and use them to actively collect, transport and deposit pollen on host flowers to ensure food for their seed-feeding larvae (Kato et al. 2003;Kawakita and Kato 2006;Kawakita et al. 2015). Epicephala moths are the only documented pollinators for many of these hosts, making this interaction an obligate mutualism. A number of Epicephala species have secondarily lost the pollination behavior and became parasitic (Kawakita and Kato 2009;Kawakita et al. 2015), which is often accompanied by the loss of the specialized sensilla on the proboscis (Kawakita et al. 2015).
Glochidion, Breynia and Phyllanthus belong to the well-defined tribe Phyllantheae, which contains over 1,200 species globally (Hoffmann et al. 2006). Of these, ca. 500 species are thought to depend exclusively on Epicephala for pollination (Kawakita and Kato 2009). Because there is high level of species-specificity between the plants and the moths (Kawakita and Kato 2006;Kawakita et al. 2010), a comparable number of Epicephala species likely exist; however, the genus currently consists of only 53 named species (De Prins andDe Prins 2005, 2014;Li and Yang 2015;. There is clearly a need to rapidly advance the taxonomy of the genus, especially because most published ecological and evolutionary studies on this mutualism treated Epicephala with arbitrary and variable names (Kawakita andKato 2004a,b, 2009;Kawakita et al. 2004Kawakita et al. , 2010Kawakita et al. , 2015Okamoto et al. 2007;Hembry et al. 2012Hembry et al. , 2013Goto et al. 2010;Svensson et al. 2010), making comparisons among studies problematic (but see Hu et al. 2011;Zang et al. 2012a;Li and Yang 2015; for recent taxonomic advancement of Chinese Epicephala).
Aside from the remarkable pollination behavior, Epicephala is noteworthy among other genera of Gracillariidae in being seed parasitic and having a well-developed ovipositor (Kato et al. 2003). Gracillariid moths are predominantly leaf miners; the seed-feeding habit is otherwise only known in Conopomorpha Meyrick, 1885, which contains species that attack seeds of tropical fruit trees such as lychee and longan (both Sapindaceae) and cacao (Malvaceae). The recently described Conopomorpha flueggella Li, 2011, which feeds on the seeds of Flueggea suffruticosa (Phyllanthaceae) (Hu et al. 2011), is distantly related to other members of Conopomorpha but closely related to Epicephala . Thus, the evolution of seed feeding and the colonization of Phyllanthaeae likely occurred in the common ancestor of Epicephala and Conopomorpha flueggella, followed by the evolution of pollination behavior, sensilla-bearing proboscis and ovipositor in Epicephala. Ovipositors are used by female Epicephala to deposit eggs internally in floral tissue (Kato et al. 2003;Kawakita et al. 2015), unlike other members of Gracillariidae that oviposit externally. Internal oviposition is secondarily lost in Epicephala vitisidaea Zhang, 2012 andE. mirivalvata Li, Wang &Zhang, 2012 that lay eggs in the narrow space between the tepals and ovary (Kawakita and Kato 2004;Zang et al. 2012b), although functional ovipositors are retained in both species.
The purpose of this paper is to provide descriptions of the Epicephala species occurring in Japan, where most published ecological studies have been conducted. The names used in published studies to refer to each species described here are also given to facilitate the interpretation of published results.

Methods
A total of 496 adult pinned specimens were used for this study, from which 132 genital dissections were made. Descriptions focused on the adult stage because adults provide a wealth of morphological traits useful for diagnosis and because immature stages of Epicephala are poorly known. For genital dissections, the whole abdomen was removed and incubated for 2-4 h in 10% KOH, and residual scales and soft parts were removed in 70% ethanol. Genitalia were then stained in fuchsin acid for 30 min to 2 h, dehydrated in a series of 70−100 % ethanol and mounted in Euparal (Waldeck GmbH & Co. KG, Division Chroma, Münster, Germany) on a glass slide. To study the sensilla on the proboscis, the entire head was removed, incubated in KOH as above and mounted in Euparal on a glass slide without staining. Observation and measurements were made under an Olympus BX53F microscope at 10-40× with the aid of a micrometer scale.
Images of adults were captured using the Olympus E-330 camera mounted on Olympus SZX10 dissection microscope, and those of genitalia and mouthparts were captured using the Canon EOS Kiss X5 camera mounted on the Olympus BX53F microscope. Images were taken at various depths and subsequently stacked using the CombineZP software (www.hadleyweb.pwp.blueyonder.co.uk). All images were then edited with Adobe Photoshop CC into final figures.
To infer the phylogenetic positions of the Japanese species within Epicephala, we assembled published nucleotide sequence data for the cytochrome oxidase subunit 1 (COI), arginine kinase (ArgK) and elongation factor 1-alpha (EF1α) genes available in GenBank for 52 Epicephala species (accession numbers are provided in Suppl. material 1), and used them to reconstruct the phylogeny of the genus. Sequence data are already available for the nine Epicephala species treated in this study (Kawakita andKato 2006, 2009), but they have not been analyzed together with those of other Epicephala for which data are available. Because a large number of Epicephala sequences are presently available in Gen-Bank, only one sequence per species per locus was sampled for the analysis. The COI, ArgK and EF1α gene partitions consisted of 582 bp, 723 bp and 522 bp, respectively. Phylogeny was constructed using the maximum-likelihood method in Treefinder (Jobb 2011) with substitution models proposed by the program (GTR+G, J3+G and J2+G for COI, ArgK and EF1α, respectively). Robustness of the tree was validated by a bootstrap analysis in Treefinder with 1,000 replicates. Conopomorpha flueggella was included in the analysis, and Stomphastis labyrinthica (Meyrick, 1918), Melanocercops ficuvorella (Yazaki, 1926) and Cuphodes diospyrosella (Issiki, 1957) served as outgroups .
It was observed that Epicephala species that oviposit through the ovary wall possess a characteristic angular ovipositor tip, therefore it was tested whether there was a correlation between oviposition site and ovipositor morphology using the Pagel's (1994) correlation method as implemented in the Mesquite software (Maddison and Maddison 2015). Because data on oviposition site and ovipositor morphology are also available for E. lativalvaris Li, Wang & Zhang, 2012(Zang et al. 2012a, these were included in the analysis. Oviposition site was categorized as either (1) oviposition through ovary wall or (2) oviposition in stylar tissue or external. Ovipositor morphology was categorized as either (1) angular or (2) non-angular. Using the maximumlikelihood phylogeny obtained as described above, we tested whether correlated evolution is more likely than the null hypothesis of independent evolution using Mesquite.
The level of intra-and interspecific divergences in the COI barcoding region (same as the above 582-bp fragment) was also quantified by analyzing all Epicephala barcode sequences presently available in GenBank. For each of the nine Epicephala species, the maximum pairwise distance was calculated within species and the minimal distance to other species. We also reconstructed a maximum-likelihood phylogeny in Treefinder to test for the monophyly of each species, following the method described above for the multi-gene data set. The GTR+G substitution model was chosen for the analysis.
All type materials have been deposited in the Zoological Collection of the Kyoto University Museum (KYO). Unless otherwise stated, specimens were collected by the primary author. All botanical names follow Govaerts et al. (2000).  (Kawakita and Kato 2009;Kawakita et al. 2015); Epicephala sp. 2 (G. acuminatum) .

Males
Diagnosis. This species is morphologically similar to E. eriocarpa Li, Wang & Zhang, 2012 but differs from the latter in having a longer and apically acute sacculus, lamella postvaginalis with distal arms stretched outwardly, and shorter ductus bursae relative to antrum. Description. Wingspan: 9.2-11.0 mm. Head: With numerous white scales on dorsal surface. Labial palpus with dark brown scales. Antenna brown, about 1.2× as long as forewing. Female proboscis with a large number of trichoid sensilla; sensilla 1.5× as long as width of proboscis, denser toward base.
Thorax: White dorsally. Forewing brown with narrow white band on dorsum from base to 2/3 of entire length; three pairs of white bands beginning at costal and dorsal margins near 1/2 to 3/4 length of wing and extending obliquely toward wing apex, terminating before reaching mid-width of wing; a narrow silver band with metallic reflection extending from costa to dorsum at 5/6 length; distal 1/6 orange-brown with black dot centrally, franked by short white spot or band near costa and dorsum; distal end fringed with narrow white band; cilia grayish brown. Hindwing brown, 0.8× length of forewing; cilia grayish brown.
Male genitalia: Tegumen rounded triangular. Cucullus rectangular oblong, apex rounded, inner surface covered with numerous hairs; dorsal margin longer than ventral margin. Sacculus 0.7× length of cucullus, wider than cucullus near base but abruptly tapering at mid-length, acute apically; inner surface of dorso-distal portion with minute sclerotized teeth. Vinculum U-shaped; saccus slender, 5/6 length of vinculum. Aedeagus straight; lateral surface with a pair of sclerotized longitudinal ridges near mid-length, fringed by a few spines.
Female genitalia: Lamella postvaginalis H-shaped, about 0.5× length of seventh abdominal segment, 4× as broad as ostium bursae; distal arms longer than basal arms and stretched outwardly. Antrum long, as long as lamella postvaginalis. Ductus bursae 1.6× length of antrum, with longitudinal parallel ridges for its entire length. Corpus bursae oval, as long as ductus bursae; signum triangular, at 1/3 from base. Apophyses posteriores about 1.5× length of apophyses anteriores. Ovipositor dentate laterally, rounded apically. Distribution. Found in a few islands with high elevation in the Ryukyu Archipelago (Amami Island and Okinawa Island; Fig. 9A). The host plant Glochidion acuminatum is distributed throughout Southeast Asia from southern Japan to India, so this species is likely to be found in other parts of the host plant's range.
Etymology. The name anthophilia (an adjective) is derived from the Latin antho-(= flower) and -philia (= love, affection), commemorating that the flower-visiting behavior of Epicephala was first found in this species (Kato et al. 2003).
Remarks. The flight period of this species is restricted to a 3-4 week period in May in Amami Island, corresponding to the flowering period of its host plant G. acuminatum. The egg undergoes a prolonged dormancy in the flower for up to five months, slide No. AK292). Scale bar: 1 mm. and the larva hatches and develops as the fruit begins to mature in late October ). The moth overwinters as pre-pupa. Epicephala anthophilia is presently the only known univoltine species in the genus. Diagnosis. This species is distinctive among other species of Epicephala in that the anterior margin and midline of the seventh sternite of females have strong sclerotized wrinkles. The species is similar to E. lanceolatella but can be distinguished from the latter by the apically rounded sacculus, stronger wrinkles on seventh sternite of females and broader lamella postvaginalis. Description. Description as in Zhang et al. (2012a), except the following. Head: Female proboscis with a large number of trichoid sensilla; sensilla 1.5× as long as width of proboscis, denser toward base.

Epicephala bipollenella
Male genitalia: Aedeagus slightly curved downwardly; dorsal surface with a sclerotized longitudinal ridge beginning medially at base and curving left toward apex.
Remarks. Zhang et al. (2012a) suggest that this species pollinates two Glochidion species (G. zeylanicum and G. hirsutum, hence the name bipollenella). However, G. hirsutum is a name used to refer to hairy individuals of G. zeylanicum, which occur in low frequency in some populations. Similar co-occurrence of glabrous and pubescent individuals is common in Glochidion (A. Kawakita, personal observation). This species is therefore better viewed as a specialist of G. zeylanicum, at least in populations thus far studied.   (Kawakita et al. 2004); Clade 5 (Kawakita and Kato 2006); Epicephala sp. 6 (G. lanceolatum) ).
Diagnosis. This species is very similar to E. bipollenella but can be distinguished from the latter by the apically acute sacculus, the more curved distal appendages on sacculus and broader lamella postvaginalis. Description. Wingspan: 8.8-10.3 mm.
Head: With numerous white scales on dorsal surface. Labial palpus dark brown. Antenna brown, about 1.2× as long as forewing. Female proboscis with a large number of trichoid sensilla; sensilla 1.5× as long as width of proboscis, denser toward base.
Thorax: White dorsally. Forewing brown with narrow white band on dorsum from base to 2/3 of entire length; three narrow white bands beginning at dorsal margin near 1/2 to 3/4 length of wing and extending obliquely toward wing apex, terminating before reaching mid-width of wing; white spots scattered on costal half; a narrow silver band with metallic reflection extending from costa to dorsum at 5/6 length; distal 1/6 orange-brown with black dot centrally, franked by short white band near dorsum; distal end fringed with narrow white band; cilia grayish brown. Hindwing brown, 0.8× length of forewing; cilia grayish brown.
Male genitalia: Tegumen elongated triangular. Cucullus rounded rectangular; inner surface covered with numerous hairs. Sacculus as long and wide as cucullus, acute apically; dorsal margin rounded medially, attached with a plate possessing short spines sparsely on inner surface and terminating distally as inward hook-like projection with dense spines on dorso-ventral surface. Vinculum V-shaped; saccus oval, about 2/5 length of vinculum. Aedeagus slightly curved downwardly; dorsal surface with a sclerotized longitudinal ridge beginning medially at base and curving left toward apex.
Material   Thorax: White dorsally. Forewing brown with narrow white band on dorsum from base to 2/3 of entire length; three narrow white bands beginning at dorsal margin near 1/2 to 3/4 length of wing and extending obliquely toward wing apex, terminating before reaching mid-width of wing; dull white spots scattered on costal half; a narrow silver band with metallic reflection extending from costa to dorsum at 5/6 length; distal 1/6 orange-brown with black dot centrally, franked by short white band near dorsum; distal end fringed with narrow white band; cilia grayish brown. Hindwing brown, 0.8× length of forewing; cilia grayish brown.
Male genitalia: Tegumen elongated rounded triangular. Cucullus rounded rectangular at distal half, projected outwardly at basal half with dense spines on outer surface of the projection; ventral margin of basal half folded inwardly; inner surface covered with numerous hairs. Sacculus rounded triangular, 2/3 length of cucullus, with row of long spines on ventral inner surface running parallel to ventral margin and continuing to a cluster of spines at apex. Vinculum U-shaped; saccus oblong, as long as vinculum. Aedeagus slightly curved dorsally at middle, with a pair of half-moon-shaped projections ventrally near mid-length, dorsally with parallel longitudinal ridges for entire length, dilated slightly at apex.
Female genitalia: Lamella postvaginalis rigid, crescent-shaped, curved ventrally, with a pair of teeth on posterior margin, as broad as and 0.5× length of seventh sternite. Antrum 1.2× length of lamella postvaginalis, with a pair of sclerotized parallel ridges continuing to ductus bursae. Ductus bursae as long as antrum, with longitudinal parallel ridges to 2/3 of its length. Corpus bursae elongate oval; signum absent. Known host and adult behavior. Known only from Glochidion lanceolatum. Pollination behavior present. Oviposition through ovary wall, in space between the wall and ovule (Fig. 8E). Larva feeds on seeds.
Etymology. The name perplexa is the female form of the Latin adjective perplexus (= cryptic), because this species remained hidden until a detailed study on species specificity was performed (Kawakita and Kato 2006).
Remarks. This species occurs in full sympatry with E. lanceolatella. The two species may even emerge from the same single fruit. Known ecological difference between the two species is limited to the oviposition behavior, but the difference in the level of sensilla development on the proboscis (Fig. 7) may indicate that this species delivers less pollination benefit than E. lanceolatella. Whereas the close relatives of E. lanceolatella use plants having close affinity to G. lanceolatum, E. perplexa is distantly related to these Epicephala species (Fig. 10). Thus, the original pollinator of G. laceolatum has likely been E. lanceolatella, and E. perplexa has shifted onto G. laceolatum more recently. Diagnosis. This species is similar to E. camurella  in having dented cucullus, distal projection on sacculus with dense spines, bilobed lamella postvaginalis, smooth  antrum and triangular signa. However, the former clearly differs from the latter in distal projection on sacculus being finger-shaped and each lobe on lamella postvaginalis being club-shaped.

Epicephala obovatella
Description. Wingspan: 7.5-11.0 mm. Head: With numerous white scales on dorsal surface. Labial palpus dark brown. Antenna brown, about 1.2× as long as forewing. Female proboscis with a large number of trichoid sensilla; sensilla 1.5× as long as width of proboscis, denser toward base.
Thorax: White dorsally. Forewing brown with narrow white band on dorsum from base to 2/3 of entire length; three pairs of narrow white bands beginning at costal and dorsal margin near 1/2 to 3/4 length of wing and extending obliquely toward wing apex, terminating before reaching mid-width of wing; a narrow silver band with metallic reflection extending from costa to dorsum at 5/6 length; distal 1/6 orange-brown with black dot centrally, franked by short white band near dorsum; distal end fringed with narrow white band; cilia grayish brown. Hindwing brown, 0.8× length of forewing; cilia grayish brown.
Male genitalia: Tegumen rectangular, acute at apex. Cucullus rounded rectangular, dented at ventral margin at 3/4 of its length; inner surface covered with numerous hairs. Sacculus rounded trapezoid, 0.6× length of cucullus; dorsal margin attached with a narrow plate terminating distally as an inward finger-like projection with a row of spines dorso-ventrally. Vinculum U-shaped; saccus oblong, acute at apex, 0.8× length of vinculum. Aedeagus straight; cornutus absent.
Female genitalia: Lamella postvaginalis strongly bilobed; each lobe club-like, dilated outward, about 0.5× length and width as seventh sternite. Antrum broad, 0.2× width of seventh sternite, as long as lamella postvaginalis, smooth on surface. Ductus bursae 1.8× length of lamella postvaginalis, with bundle of longitudinal parallel ridges for its entire length. Corpus bursae oval, as long as buctus bursae; signum triangular, located medially. Apophyses posteriores 1.5× length of apophyses anteriores. Ovipositor dentate laterally, angular at apex. Known host and adult behavior. Glochidion obovatum (mainland Japan, Yaku Island and Kume Island) and G. rubrum (Yonaguni Island and Taiwan), which are parapatric sister species. Pollination behavior present. The egg is laid through the ovary wall between the wall and ovule (Fig. 8F). Larva feeds on seeds.
Distribution. Occurs throughout the warm temperate to subtropical regions of Japan (Fig. 9D). Recorded also from Taiwan.
Etymology. The name obovatella (an adjective) derives from the species name of the primary host plant G. obovatum. Remarks. The Taiwanese population of this species is genetically divergent from the Japanese population (>4% divergence in COI; Table 1 and Suppl. material 2). However, they are morphologically indistinguishable (Kawakita and Kato 2006), so we tentatively consider the Taiwanese population as E. obovatella.

Diagnosis.
The male genitalia of this species are distinctive and have no parallel in other known species; sacculus possesses a thick spine on apex and a cluster of long spines on dorsal projection. The large, round lamella postvaginalis also distinguishes this species from other known Epicephala. Description. Wingspan: 7.2-8.8 mm.
Head: With numerous white scales on dorsal surface. Labial palpus dark brown. Antenna brown, about 1.2× as long as forewing. Female proboscis with a large number of trichoid sensilla; sensilla 1.5× as long as width of proboscis, denser toward base.
Thorax: White dorsally. Forewing brown with narrow white band on dorsum from base to 2/3 of entire length; two pairs of narrow white bands beginning at costal and dorsal margin near 1/2 to 3/4 length of wing and extending obliquely toward wing apex, terminating before reaching mid-width of wing; dorso-distal band accompanied by another parallel band of same size on distal position; a narrow silver band with metallic reflection extending from costa to dorsum at 5/6 length; distal 1/6 orange-brown with black dot centrally, franked by short white band near dorsum; distal end fringed with narrow white band; cilia grayish brown. Hindwing brown, 0.8× length of forewing; cilia grayish brown.
Male genitalia: Tegumen oblong, acute at apex. Cucullus rectangular oblong; ventral margin with acute tip at mid-length terminating with short spine; inner surface covered with numerous hairs. Sacculus ovoid; apex sharply concave, with a long spine on ventral half; basal part of dorsal margin attached with a narrow plate terminating distally as an inward, finger-like projection with 3 or 4 long spines directing dorso-ventrally. Vinculum U-shaped; saccus broad, 0.3× width of vinculum, as long as vinculum, oblong and acute at apex. Aedeagus straight, slightly dilated toward apex; cornutus absent.
Female genitalia: Lamella postvaginalis long and broad, 0.8× width and length of seventh sternite, coarsely dentate at distal end. Antrum broad, 0.4× width and length of lamella postvaginalis, smooth on surface. Ductus bursae as long as seventh sternite, with cluster of longitudinal parallel ridges for its entire length. Corpus bursae oval to elongate oval, as long as buctus bursae; signum absent. Apophyses posteriores 1.5× length of apophyses anteriores. Ovipositor dentate laterally, angular at apex.
Etymology. The species name corruptrix (a noun in apposition) was inherited from Tegeticula corruptrix, a derived parasitic species of yucca moth (Pellmyr et al. 1999). Epicephala corruptrix has a potential to corrupt the mutualistic relationship with its host because the species induces gall formation in pollinated flowers which then hardly produce seeds (Fig. 11).
Remarks. This species shares the same host plant with E. obovatella, but E. obovatella has not been collected from any of the locations where E. corruptrix occurs (Fig.  9). Because of the limited mutualistic potential of this species, reproduction of the host plants (G. obovatum and G. rubrum) is likely to be severely limited on islands where E. corruptrix occurs, in comparison to locations where E. obovatella is present.
Diagnosis. Lamella antevaginalis of this species forms a sclerotized complete circle around ostium, a character that cannot be found in any other species of Epicephala. Cornuti of short thick spines occurring dorsally and ventrally on distal portion of aedeagus are also distinctive of this species. Description. Description as in Zhang et al. (2012a), except the following. Head: Female proboscis with a large number of trichoid sensilla; sensilla 1.5× as long as width of proboscis, denser toward base.
Male genitalia: Cornuti on aedeagus occurring dorsally and ventrally; dorsal cornuti consisting of 4-6 short spines, shorter than 0.7× width of aedeagus; ventral cornuti a pair of thick and long spines, longer than width of aedeagus.

Known host and adult behavior.
Known only from Breynia vitis-idaea. The adult is the pollinator of the host plant (Kawakita and Kato 2004b). Eggs are placed in the interspace between the tepal and ovary (Fig. 8H), so the ovipositor does not penetrate floral tissue. Larva feeds on seeds.
Distribution. In Japan occurs widely in the Ryukyu Archipelago (Fig. 9E). Known also from China (Zhang et al. 2012a).
Diagnosis. Sexually dimorphic color pattern and fused seventh sternite and tergite are thus far unknown in any species of Epicephala, making this species highly distinctive within the genus. Overall small size, row of thick spines on ventral margin of cucullus, long spine at cucullus base and numerous short spines on inner cucullus add to the uniqueness of this species in the genus. Description. Wingspan: 5.7-7.5 mm.
Head: Females with numerous grayish brown scales on dorsal surface; males with numerous white scales. Labial palpus dark brown to black in females, dark brown in males. Antenna dark brown in females, grayish brown in males, about 1.2× as long as forewing. Trichoid sensilla on female proboscis rudimentary, shorter than width of proboscis, less than 30 per galea.
Thorax: Brown dorsally in females, white in males. Forewing of females dark brown with narrow white band on dorsum from base to 1/4 of entire length, medially with narrow white band extending from costa to dorsum; a pair of narrow white bands beginning at costal and dorsal margin near 2/3 of wing and extending obliquely toward wing apex, terminating before reaching mid-width of wing; a narrow silver band with metallic reflection extending from costa to dorsum at 5/6 length; distal 1/6 brown with black dot centrally; distal end fringed with narrow white band and terminating with narrow black band; cilia dark brown. Hindwing of females dark brown, 0.8× length of forewing; cilia dark brown. Forewing of males brown with narrow white band on dorsum from base to 2/3 of entire length; three pairs of narrow white bands beginning at costal and dorsal margin near 1/2 to 3/4 length of wing and extending obliquely toward wing apex, terminating before reaching mid-width of wing; a narrow silver band with metallic reflection extending from costa to dorsum at 5/6 length; distal 1/6 orangebrown with black dot centrally, franked by short white band near dorsum; distal end fringed with narrow white band and terminating with narrow brown band; cilia grayish brown. Hindwing of males brown, 0.8× length of forewing; cilia grayish brown.
Male genitalia: Tegumen rounded triangular. Cucullus rectangular oblong; ventral margin medially concave; basal 1/3 of cucullus fringed with long spines on ventral margin; spines longer than width of cucullus; another distinctly long spine occurring at ventral base of cucullus, 1/2 length of cucullus; distal half of cucullus with numerous short spines on inner surface and few hairs. Sacculus broad, 2× width of cucullus, 0.7× length of cucullus, distinctly concave at apex; concave portion of apex fringed with setae; inner wall of sacculus abruptly projecting inward and curved toward dorso-caudal direction, pointed apically; ventral edge of projection fringed with setae. Vinculum U-shaped; saccus thin and rod-shaped, 0.6× length of vinculum. Aedeagus straight; cornutus absent.
Female genitalia: Seventh sternite completely fused to seventh tergite to form a cylindrical segment. Caudal end of seventh sternite with row of parallel latitudinal ridges. Lamella postvaginalis trapezoid, dilated toward apex, small, 0.3× width and length of seventh sternite, slightly convex and weakly dentate on caudal margin. Antrum smooth, 0.2× width and 0.5× length of seventh sternite. Ductus bursae as long as seventh sternite, with short lateral sac at base; surface of sac and franking portion of Figure 10. Maximum-likelihood phylogeny of Epicephala species based on sequences of the COI, ArgK and EF1α genes. Numbers above nodes are maximum-likelihood bootstrap support values based on 1,000 replications. The Japanese Epicephala species are marked in blue. Symbols right to species names donate ovipositor morphology: inverted U-shape, rounded apically; inverted V-shape, acute apically. ductus bursae with numerous teeth on surface. Corpus bursae elongate oval, as long as combined antrum and ductus bursae; signum absent. Apophyses posteriores 1.7× length of apophyses anteriores. Ovipositor dentate laterally, angular at apex.
Distribution. Widely distributed in the Ryukyu Archipelago, Japan (Fig. 9F). The host plant Phyllanthus lepidocarpus is a common weed along roadsides and in cultivated land. Although P. lepidocarpus also occurs in mainland Japan, E. parasitica has only been found in the Ryukyu Archipelago.
Etymology. The name parasitica is the female form of the Latin adjective parasiticus (= parasitic), in reference to the parasitic nature of the species.
Remarks. This and the following species (E. nudilingua) belong to a derived clade of Epicephala specialized to herbaceous species of Phyllanthus (Fig. 10). Pollination behavior has not been observed in any of the species in this clade, so they are pure parasites that derived from a pollinating ancestor (Kawakita and Kato 2009).

Diagnosis.
Aside from E. parasitica, this species is smaller than any other known species of Epicephala. Exaggerated cornutus, spiracle on seventh tergite, bilobed lamella postvaginalis and heavily sclerotized and curved antrum, clearly distinguish this species from other known Epicephala.
Thorax: Grayish white dorsally. Forewing dark brown with narrow white band on dorsum from base to 1/3 of entire length; three pairs of narrow white bands beginning at costal and dorsal margin near 1/2 to 3/4 length of wing and extending obliquely toward wing apex, terminating before reaching mid-width of wing; a narrow silver band with metallic reflection extending from costa to dorsum at 5/6 length; distal 1/6 brown with black dot centrally, franked by narrow white band near dorsum; distal end fringed with narrow white band and terminating with narrow dark brown band; cilia grayish dark brown. Hindwing dark brown, 0.8× length of forewing; cilia grayish dark brown.
Male genitalia: Tegumen rounded triangular. Cucullus rectangular oblong, dilated at apex, covered with numerous hairs on inner surface; ventral base with small out-  Oviposition behavior has not been observed in the wild. Floral dissection suggests that the egg is laid in young fruit through the ovary wall between the wall and ovule. Larva feeds on seeds.
Distribution. Known only from three populations in Tochigi, Tokyo and Oita Prefecture, Japan (Fig. 9F). The host plant P. ussuriensis is widespread in the temperate regions of Japan and other parts of East Asia, so the species is likely to be found elsewhere. The plant was common at damp habitats in flood plains before 1980s but is now uncommon and locally threatened in Japan.
Etymology. The name nudilingua (a noun in apposition) derives from the Latin nudus (= naked) and lingua (= tongue) in reference the hairless proboscis of the female, which is a derived condition in Epicephala.

Phylogenetic results
Phylogenetic analysis of the 53 Epicephala species resulted in a fairly resolved phylogeny (Fig. 10), consistent with previous phylogenetic analyses of Epicephala (Kawakita and Kato 2009;Kawakita et al. 2010Kawakita et al. , 2015Hembry et al. 2013). Conopomorpha flueggella was recovered as sister to one of the two clades comprising the New Caledonian Epicephala species. The Japanese species belong to either one of the following three well-supported clades: the clade consisting of species associated with Glochidion, the clade restricted to species found on Breynia, and the clade containing all known species attacking herbaceous Phyllanthus.
Analysis of correlated evolution between oviposition site and ovipositor morphology in Mesquite indicated that the two traits exhibit greater correlation than expected under the null hypothesis of independent evolution (P < 0.001).
Maximum pairwise divergence in DNA barcode within species was generally low (< 1%) with the exception of E. obovatella that exhibited moderate divergence (4.12%) between populations in Japan and Taiwan (Table 1; Kawakita and Kato 2006). Nevertheless, all Epicephala species for which multiple DNA barcodes were available were strongly recovered as respectively monophyletic groups in the ML phylogeny (Suppl. material 2). Minimum distances to heterospecifics were 4.12-6.53% for the nine Epicephala species studied (Table 1).

Discussion
The nine species of Epicephala in Japan were clearly distinguishable to each other based on the morphology of both male and female genitalia, but they are usually very difficult to identify based on wing pattern. The extent of genital morphological variation of Epicephala is remarkable (also see Zang et al. 2012a;Li and Yang 2015;, especially when it is compared to that of other comparably large genera of Gracillariidae (e.g., Caloptilia) where there is very low variation in genital morphology but far greater variation in wing pattern (Kumata 1982). The morphology of the female genitalia is as diagnostic in differentiating species as that of the male genitalia, which is also uncommon in Gracillariidae. The level of interspecific genetic variation in Epicephala (Table 1) is not necessarily higher or even lower than those of other gracillariid genera (Cuphodes, 6.6-15.7%; Diphtheroptila, 7.3-11.6%; Caloptilia, 6.6-10.7%; Kawakita et al. 2010), which may indicate that genital traits in fact evolve faster in Epicephala than in other genera. The reason for this pattern is unknown, but there may be differences among lineages of Gracillariidae in the mechanism of reproductive isolation that can account for the observed pattern. Studies aimed at assessing the roles of genital morphology and wing pattern variation in reproductive isolation may be interesting.
The analysis of correlated evolution between oviposition site and ovipositor morphology suggested a clear linkage between these traits. Based on the phylogeny (Fig.  10), there have been repeated transitions in oviposition site during the diversification of Epicephala, which may indicate that shifts in oviposition site are adaptive. Because some Glochidion plants selectively abort flowers with heavy egg load and abortion is likely based on the extent of mechanical damage to flowers ; personal communication of R. Goto, University of Michigan), external oviposition in E. vitisidaea and others may have evolved to circumvent the abortion response in their host plants. By contrast, the adaptive significance of apical and lateral ovipositions is less clear. However, the observation that E. lanceolatella and E. perplexa, which co-occur on the same G. lanceolatum host, display apical and lateral ovipositions, respectively, suggests that these oviposition strategies likely represent distinct niches. Detailed study on the evolution of oviposition strategy in Epicephala may reveal previously unknown aspect of the coevolution between the moths and their hosts.
Another finding of this study that deserves further pursuit is the galling potential of E. corruptrix (Fig. 11). Because E. corruptrix possesses the pollination behavior (Kawakita and Kato 2006), it is not a pure parasite. However, the benefit they confer to the plants is likely to be very small, especially when compared with E. obovatella that uses the same G. obovatum and G. rubrum hosts in different locations (Fig. 9). Because our sampling is still limited, a study is needed to verify whether or not E. corruptrix and E. obovatella cooccur in any location and to compare their contributions to their host plant's reproduction. Epicephala corruptrix will be a good model to study how shifts in the cost/benefit balance occur in mutualisms and potentially drive the collapse of the interaction.
With the seven new species described here, the genus Epicephala now consists of 60 described species (Li and Yang 2015;. However, the number is far lower than the few hundred species estimated from ecological, molecular and biogeographical data (Kawakita 2010). Because the present study only focused on species occurring in Japan, which is near the northern end of the distribution range of Epicephala, taxonomic studies encompassing broader biogeographic regions are clearly needed. For example, the molecular phylogeny of Epicephala (Fig. 10) suggests that there are clades confined to Madagascar or New Caledonia where none of the described Epicephala species occur. These regions are known for hotspots of Phyllanthus diversity and thus potentially have large numbers of undescribed Epicephala species. There is also a high diversity of Phyllanthus in the New World where Epicephala has not been recorded previously, but recent observations suggest that Epicephala is also widespread in the Neotropics (A. Kawakita and M. Kato, unpublished data). Accelerating the taxonomy of Epicephala at a global scale is therefore highly important in facilitating the ecological and evolutionary studies of this model group.