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The species-specificity of male genitalia has been well documented in many insect groups and sexual selection has been proposed as the evolutionary force driving the often rapid, morphological divergence. The internal female genitalia, in sharp contrast, remain poorly studied. Here, we present the first comparative study of the internal reproductive system of Sepsidae. We test the species-specificity of the female genitalia by comparing recently diverged sister taxa. We also compare the rate of change in female morphological characters with the rate of fast-evolving, molecular and behavioral characters.
We describe the ectodermal parts of the female reproductive tract for 41 species representing 21 of the 37 described genera and define 19 morphological characters with discontinuous variation found in eight structures that are part of the reproductive tract. Using a well-resolved molecular phylogeny based on 10 genes, we reconstruct the evolution of these characters across the family [120 steps; Consistency Index (CI): 0.41]. Two structures, in particular, evolve faster than the rest. The first is the ventral receptacle, which is a secondary sperm storage organ. It accounts for more than half of all the evolutionary changes observed (7 characters; 61 steps; CI: 0.46). It is morphologically diverse across genera, can be bi-lobed or multi-chambered (up to 80 chambers), and is strongly sclerotized in one clade. The second structure is the dorsal sclerite, which is present in all sepsids except Orygma luctuosum and Ortalischema albitarse. It is associated with the opening of the spermathecal ducts and is often distinct even among sister species (4 characters; 16 steps; CI: 0.56).
We find the internal female genitalia are diverse in Sepsidae and diagnostic for all species. In particular, fast-evolving structures like the ventral receptacle and dorsal sclerite are likely involved in post-copulatory sexual selection. In comparison to behavioral and molecular data, the female structures are evolving 2/3 as fast as the non-constant third positions of the COI barcoding gene. They display less convergent evolution in characters (CI = 0.54) than the third positions or sepsid mating behavior (CICOI = 0.36; CIBEHAV = 0.45).
The diversity and morphology of male genitalia have been well documented in many insect taxa [1-7], and most evolutionary biologists agree that sexual selection is responsible for driving the frequent and rapid divergence of these structures [6,8-11]. In comparison to male structures, the external and internal female reproductive tract is largely a "black box" that remains poorly known. Taxonomists routinely use male but not female genitalia for species identification, and there is some evidence that female genitalia are indeed less variable than their male counterparts [12,13]. However, it is important to remember that most taxonomists are interested in studying structures that are easily accessible and preserve well under different conditions (e.g., ethanol, pinned specimens). Male genitalia, and in particular the intromittent organ, are ideal candidates, because they are external and generally well sclerotized [1,14,15]. In contrast, the part of the female reproductive tract that is interacting with the male intromittent organ and thus most likely to show species-specific differences is internal, fairly inaccessible, and membranous. It is therefore not surprising that relatively few systematists routinely study the internal female genitalia for taxonomic purposes, and much less comparative data are available for females. Here, we target the internal female reproductive tract in a comparative study across the Sepsidae (Diptera: Insecta).
The female reproductive tract has recently attracted more attention for other reasons [16-21]. It is likely involved in sexual conflict, sperm competition, and cryptic female choice [8,9,22-24] and generally acknowledged that detailed knowledge of the morphology of the reproductive organs is crucial for understanding their role in post-copulatory sexual selection [25,26]. For instance, in Diptera, some studies use morphological data for investigating post-copulatory sexual selection through female choice [e.g: Muscidae, , Dryomyzidae , and Tephritidae, ], sperm competition [e.g.: Drosophilidae, [11,26,29]] or sexual arms races [e.g.: Scathophagidae, ]. These studies indicate that females can influence paternity by differentially storing sperm from various males in separate sperm storage organs (e.g., spermathecae) and controlling which sperm is used for fertilizing eggs [19,26,30]. For example, in phlebotomine sandflies (Psychodidae), the male intromittent organ (i.e. the aedaegus) deposits sperm directly into the spermathecae, extending past the length of the spermathecal ducts [31,32]. This, however, is not the case for most Diptera where males deposit the sperm in the bursa copulatrix (i.e. the vagina) and/or close to the spermathecal duct openings . Based on studies of in-copula pairs of Microsepsis and Archisepsis, this is also the case in Sepsidae, sometimes involving the formation of an internal spermatophore [33-35].
With the exception of a few [16,22,26,36], most studies of the female reproductive tract in Diptera are based on single species and comparative data across multiple species are rare. Here, we present information on a large number of species of Sepsidae, a family of flies that is frequently used in sexual selection studies. Currently, the internal female reproductive system of Sepsidae is poorly known. Early schematic depictions are superficial or even misleading in their generalizations of the female structures [37-39]. More recently, there is photographic documentation in Kotrba  for a Sepsis specimen, as well as drawings by Ozerov  for a Themira specimen, but the most informative description thus far is by Eberhard and Huber  based on photos and drawings of several Archisepsis species. These authors document the presence of two spermathecae, a common oviduct, a vagina, a terminal sternite at the posterior end as well as an armored ovipositor wall. There are, however, disparities among the accounts. Eberhard and Kotrba identified a ventral receptacle, which is not mentioned by Ozerov. Similarly, Eberhard and Ozerov illustrated the presence of a large, dorsal vaginal sclerite/plate, which is not identified in Kotrba . In addition, Eberhard's drawing indicates the presence of a smaller anterior sclerite and a ventral sac, which are not illustrated by the other two authors. These could be a result of species-specific differences, but at this point we just do not know enough about the internal female reproductive system of this family to be certain.
The Sepsidae are an acalyptrate family of flies of the Sciomyzoidea with approximately 320 described species in 37 genera. These flies are abundant worldwide and numerous species have broad distributions that span more than one continent . Sepsid larvae and most adults are saprophagous i.e. closely associated with various decaying organic substrates. In recent years, sepsids have become models for testing sexual selection theories because they are strongly sexually dimorphic with respect to the male forelegs and terminalia and they also display elaborate courtship behavior [34,43-47]. The analysis presented here is part of a series of papers that uses a comparative approach to understanding the "creative powers" of sexual selection in diversifying morphology and behavior [47-50]. We provide the first comparative study of the internal female reproductive tract across Sepsidae (41 species representing 21 of the 37 described genera), using microscopic techniques that have been optimized to reveal even delicate structures such as the ventral receptacle.
Our study has three main aims. First, we investigate whether the internal female genitalia are species-specific in Sepsidae. For this purpose we include eight sister-species pairs that are very closely related based on morphological (male genitalia, male forelegs) and/or DNA sequence evidence. Second, we reconstruct the evolution of the female tract in Sepsidae by assembling a matrix based on characters describing the morphological variation in females and mapping it onto molecular [48,51] and morphological [52-54] phylogenetic hypotheses. We recently also published a comparative study on sepsid mating behavior  that documented rapid evolution and high levels of convergent evolution in behavioral characters that were comparable to fast evolving molecular characters such as the third positions in protein encoding mitochondrial genes. Our third aim is to assess whether the female reproductive system evolves similarly fast. We thus compare the number of character changes and quantify the level of convergence in our data set with the amount of change in mating behavior and the DNA barcoding gene used for species-identification [55,56]. We also identify and describe fast-evolving female structures that are likely candidates for future studies of post-copulatory sexual selection in Sepsidae.
We studied 41 species representing 21 of the 37 described genera (Table (Table1).1). To test the species-specificity of female structures, we included eight sister-species pairs that are closely related according to either male structures and/or DNA sequence evidence: (1) The common Holarctic Themira biloba and T. putris are morphologically so similar that they were considered one species until 1975 (Andersson, 1975); (2) Meroplius fukuharai was only described in 1984 because it is very similar to M. minutus . The remaining sister pairs differ by <2% for the DNA barcoding gene COI (see discussion): (3) Dicranosepsis emiliae &D. hamata, (4) Sepsis cynipsea &S. neocynipsea, (5) S. duplicata &S. secunda, (6) S. fulgens &S. orthocnemis, (7) S. punctum &S. monostigma, and (8) T. flavicoxa &T. lucida .
Our investigation of the female reproductive tract is primarily based on dissections of freshly killed and alcohol-preserved specimens. Only for Susanomira caucasica did we use pinned material (Table (Table1).1). Live flies were killed either by freezing or with a killing jar and dissected immediately in Ringer's solution under a Leica MZ16 microscope, while alcohol preserved and pinned specimens were macerated in KOH prior to dissection. Details on the external morphology of the female genitalia were not included in this study as there was not much change across the family. After dissection, we removed the internal reproductive tracts and mounted them, usually in a dorsoventral orientation, on glass slides in polyvinyl-lactophenol with an admixture of chlorazol black E. This medium progressively macerates the soft tissue while staining unsclerotized cuticular elements of the specimen blue. Dissections of fresh material yielded better results especially with respect to the membranous parts. Nonetheless, macerated specimens were sufficient for identifying the most important structures.
The slide preparations were studied under bright field and differential interference contrast (DIC) using a Zeiss Axioskop 2 equipped with a drawing tube as well as a Zeiss AxioCam digital camera. We prepared schematic drawings as well as photographic images at high magnifications for all the species. Descriptions of the internal reproductive tract are based on one to seven dissections per species (Table (Table1).1). The drawings focus on those structures that are ectodermal in origin and are lined with cuticle, thus omitting ovaries, lateral and common oviducts. The terminology of the morphological structures follows a recent glossary by Kotrba . The term "sclerotized" refers to darkened cuticular structures that are not stained blue by chlorazol black E and appear brown under the bright field.
A character matrix was assembled for 41 sepsid species plus Willistoniella pleuropunctata (Ropalomeridae) as outgroup using MacClade 4.0 . Nineteen morphological characters were defined based on the discontinuous variation of the female reproductive tract (Table (Table2).2). In order to test for species-specificity, we used the matrix to identify species that have identical character scores for the discontinuous variation. For these species pairs, we then assessed whether morphological structures with continuous variation across the family allowed for the differentiation of these species. In addition, using PAUP* , we calculated the uncorrected pairwise distances based on our female morphological data set as well as the distances for the COI barcoding gene  in order to compare the amount of character change across multiple data sets.
There is indication in sepsids that the phylogenetic signal from molecular sequences can conflict with that of morphological data . We therefore mapped our female morphological characters onto two different phylogenetic hypotheses. Using PAUP* , we generated a molecular phylogeny based on DNA sequence data of 10 gene fragments from Ang et al. and Su et al. (87 sepsid species + 2 outgroups; heuristic search; 100 random stepwise additions; TBR branch swapping). A new analysis was needed to place the recently described Perochaeta dikowi, which is included in our study and whose DNA sequence data was added to Su et al.'s data using the concatenation software SequenceMatrix . We also mapped the characters onto an earlier morphological phylogeny that was reconstructed based on egg, larval, and adult characters [52-54]. Our study of the female reproductive system has complete taxon overlap with the molecular phylogeny, while only 38 species are shared with the morphological tree; i.e., some species had to be deleted for the pairwise comparison with the morphological tree. The character mapping was performed in MacClade 4.0  and we recorded the amount of change (tree length) and level of homoplasy as quantified by the consistency index (CI). Given that taxon number was kept constant in the pairwise comparisons, this avoids the problem of a negative correlation between CI and the number of terminals .
To estimate the rate of change in the internal female reproductive characters, we compared our female morphological data set with other characters that are known to evolve fast such as the third positions of the mitochondrial DNA barcoding gene  and sepsid mating behavior . We split the COI barcoding gene according to codon positions and obtained a character set containing only the non-constant third positions in order to ensure comparability to our morphological data, which also includes only non-constant characters. Due to incomplete taxon overlap between the behavior and female morphology data, we could only include the 22 species for which both data are available (Table (Table1).1). In MacClade 4.0 , we subsequently mapped all the different characters on the molecular phylogeny derived from the earlier-mentioned phylogenetic analysis. In order to assess the degree of homoplasy in our female reproductive characters, we mapped them onto the molecular phylogeny and calculated the number of observed steps over the minimum number of steps. This value quantifies the level of homoplasy and is the inverse of the consistency index. We repeated this for both the molecular and behavioral data set.
In addition, we split the morphological characters relating to the female reproductive tract according to different reproductive structures (e.g.: ventral receptacle, dorsal sclerite, spermathecae, etc.) and mapped them separately on the molecular tree in order to quantify the amount of change contributed by the individual structures.
Our description is restricted to the cuticular elements of the reproductive tract, which are: the tubular vagina (va), paired dorsal spermathecae (sp) and accessory glands (ag), the dorsal sclerite (ds; absent in Orygma luctuosum and Ortalischema albitarse), the ventral receptacle (vr), the ventral evagination (ve), the tubular inverted ovipositor (ov), and the internalized sternite VIII (St VIII). Please refer to the figures figures1,1, ,2,2, ,3,3, ,4,4, ,5,5, ,6,6, ,7,7, ,8,8, ,99 and and1010 when reading and evaluating the descriptive text.
The vagina is an elongate muscular tube lined internally with thin cuticle. It is anteriorly fused with the common oviduct (oc). The spermathecal ducts and the ducts of the accessory glands respectively open anterodorsally and posterolaterally into the vagina (Figure (Figure1).1). This region of the vagina wall associated with the duct openings is, with the exception of Ortalischema albitarse and Orygma luctuosum (Figure (Figure6),6), modified into a dorsal sclerite (ds), which can be very diverse in shape and degree of sclerotization. In some species, additional paired sclerotizations [e.g.: Sepsis fulgens (Figure (Figure1)1) and Themira biloba (Figure (Figure9)]9)] occur in the posterior dorsal vaginal wall. Directly opposite to the spermathecal duct openings, the anteroventral portion of the vagina gives rise to the ventral receptacle and, directly posterior to this, the ventral evagination. When the vagina is empty, its wall forms numerous folds. This allows the vagina to become greatly extended when containing a spermatophore after copulation or, in the case of viviparous species, a developing egg or larva . In our dissections we observed the vagina to contain spermatophores in some species [e.g: Allosepsis indica, Australosepsis niveipennis, Sepsis dissimilis and S. thoracica] and a single developing egg in Themira minor (Figure (Figure1010).
The vagina tapers and opens into the likewise tubular ovipositor, which, together with sternite VIII, is invaginated from the body surface between sternite VII and the terminalia. In some species, the apical portion of sternite VIII is clearly bifurcated, while in others it is fused. The ovipositor wall is, with the exception of Toxopoda and Platytoxopoda, internally ornamented to a variable degree with spines or tiny denticles that may be arranged as singles, clusters or rows (Figure (Figure22).
All sepsids have two strongly sclerotized spermathacae that are usually round, although ovoid, mushroom- and barrel-shaped forms also occur. They are at times highly telescoped [e.g: Allosepsis indica (Figure (Figure4)4) and Themira superba (Figure (Figure10)].10)]. The spermathecal capsules can be of equal or, more often, of distinctly unequal size. In one species, Toxopoda sp., we found the spermathecal capsules to be almost entirely reduced (Figure (Figure10).10). Moreover, in some species their wall is ornamented with transverse wrinkles or spines [e.g.: Paratoxopoda amonanae (Figure (Figure6)6) and Platytoxopoda (Figure (Figure7)7) respectively]. The latter are usually connected to cuticular end apparatuses of gland cells in the surrounding glandular tissue. In Ortalischema albitarse, the spermathecae have a particularly elaborate shape with a belt of spines around their perimeter and an apical spiny crown (Figure (Figure66).
The spermathecal ducts can likewise be either equal or unequal in length. They can (i) open near to each other but separately into the dorsal vaginal wall [e.g.: Themira biloba (Figure (Figure9)],9)], or (ii) open into a common pouch of the vagina wall, sometimes together with the accessory gland ducts [e.g.: Archisepsis scabra (Figure (Figure4)].4)]. This pouch can be of considerable length. In one species, Meroplius fukuhari, it forms a heavily sclerotized 'sleeve' that is associated with the dorsal sclerite (Figure (Figure3).3). In a few other species, the bases or the apical portions of the spermathecal ducts themselves are weakly sclerotized [e.g.: Parapaleosepsis plebeia (Figure (Figure6)6) and Saltella sphondylii (Figure (Figure77)].
The accessory glands are lined by delicate cuticle, which is surrounded by a glandular epithelium. Their size varies across species and they are at times even larger than the spermathecae [e.g.: Dicranosepsis crinita (Figure (Figure4)4) and Themira minor (Figure (Figure10)].10)]. The membranous accessory gland ducts are predominantly equal in length and shorter than the spermathecal ducts. Because of their very delicate nature they are often lost in dissections, especially after maceration, which is why they are distorted or lacking in some of our illustrations.
In all species but Ortalischema albitarse and Orygma luctuosum, the openings of spermathecal and accessory gland ducts are framed by the dorsal sclerite, whose shape most usually resembles that of an inverted heart. It varies greatly across the family and even between closely related species within a genus (Figure (Figure11).11). The difference in shape as well as in the degree and pattern of sclerotization is often difficult to describe or code as characters with discrete states. However there are some distinctive features, such as the presence of a distinct honeycomb surface ornamentation at the basal cheeks of the sclerite and the presence of a long process at its anterior part [e.g.: Paratoxopoda amonanae (Figure (Figure66)].
The ventral receptacle arises from the anteroventral portion of the vagina and extends anteriorly along the basal part of the common oviduct. It is also very variable, albeit mostly between genera (Figure (Figure12).12). In Orygma, this organ is very large and of unique shape compared to all other species. It has an elongate central rod that is quite massive and flanked by thin-walled lateral chambers (Figure (Figure6).6). Due to its significant morphological difference, this structure is difficult to homologize with structures in the other remaining species. The ventral receptacle in other sepsids, can be bi-lobed with or without additional internal subdivisions; or it can be multi-chambered with 10 to 80 separate roundish chambers. The interpretation of the multi-chambered ventral receptacle condition in Decachaetophora aeneipes was somewhat difficult, because in all seven studied specimens this structure appeared somewhat disintegrated, although delicate chambers and a diffuse apical brown spot were discernible (Figure (Figure4).4). In some species, the ventral receptacle has a more or less distinct sclerotized plate apically, and in one species, Allosepsis indica, this apical portion is enlarged to almost the size of an additional chamber (Figure (Figure4).4). In the clade Paratoxopoda + Toxopoda the ventral receptacle is completely sclerotized and has a modified stalked base (Figure (Figure66 &7 respectively).
The ventral evagination inserts posterior of the ventral receptacle. From there it extends anteroventrally past the ventral receptacle. It varies in size, sometimes projecting further than the ventral receptacle, in other species not even reaching the length of that organ [e.g.: Susanomira caucasica (Figure (Figure9)9) and Themira lucida (Figure (Figure10)10) respectively]. This structure has been termed 'ventral sac' by Eberhard and Huber .
The cuticular elements include a tubular vagina, paired, elongate spermathecae and accessory glands. However, unlike in sepsids, the ventral receptacle is tubular and a dorsal sclerite is absent. Also, there is a small ventral pouch posterior to the ventral receptacle with unclear homology. In addition, instead of an inverted ovipositor, the vagina opens posteriorly into a fused sheath formed by segment VIII and contains the cerci (Figure (Figure1010).
Based on our dissections of 41 sepsid species and the ropalomerid outgroup Willistoniella pleuropunctata, we defined 19 morphological characters describing the internal female reproductive tract and scored them across all taxa (Table (Table2;2; 11 binary, 8 multistate characters; 3 ordered, 16 unordered). The detailed character descriptions are provided as supplementary data (Additional file 1). Of the 42 species included in this study, only two pairs of taxa, Dicranosepsis distincta &D. emiliae (non-sister taxa) and Sepsis duplicata &S. secunda (sister taxa) have identical character codes for the female reproductive tract. All other species differ in at least one character.
For the eight sister-species pairs, we quantified the amount of changes separating them based on uncorrected pairwise distances (PD) derived from our female data set and the variable third positions for the COI barcoding gene. They are: (i) Dicranosepsis emiliae - D. hamata [PDFEM = 5.56%, PDCOI = 1.49%]; (ii) Meroplius fukuharai - M. minutus [PDFEM = 16.7%, PDCOI = 13.4%]; (iii) Sepsis duplicata - S. secunda [PDFEM = 0%, PDCOI = 1.97%]; (iv) S. cynipsea - S. neocynipsea [PDFEM = 5.56%, PDCOI = 1.34%]; (v) S. fulgens - S. orthocnemis [PDFEM = 5.56%, PDCOI = 0.76%]; (vi) S. monostigma - S. punctum [PDFEM = 22.2%, PDCOI = 3.25%]; (vii) Themira biloba - T. putris [PDFEM = 27.8%, PDCOI = 9.37%]; (viii) T. flavicoxa - T. lucida [PDFEM = 5.56%, PDCOI = 0.69%] (Figure (Figure9).9). Seven of these pairs exhibit greater difference in the female characters than the COI barcode (χ2 test, 1 df; p = 0.034).
Our heuristic search yielded three most parsimonious trees (19939 steps), and the strict consensus tree was pruned to include only the 42 species covered in this study. Given that the differences between the three equally parsimonious trees affect species that were not included here, the tree for our 42 species is fully dichotomous. We refer to this tree as the molecular phylogeny from this point forth (Figure (Figure13).13). Tracing our morphological characters on the molecular phylogeny with 42 taxa required 120 steps (CIMOL = 0.41). For the comparison with the morphology-based phylogeny, we had to exclude taxa not included in the morphology-based hypotheses [52-54]. After culling these, our tree included 38 taxa and the female internal reproductive characters require five more steps than on the molecular tree. Overall, we thus found that the evolution of the female internal reproductive characters is more in line with the recent molecular phylogeny (113 steps; CIMOLcul = 0.42) than the earlier morphology-based hypothesis (125 steps; CIMORPH = 0.38). Hence, we decided to use the molecular phylogeny for the subsequent discussion of character evolution (Figure (Figure1313).
The ventral receptacle morphology contributed seven of the 19 characters and accounted for 61 of the 120 steps. The remaining 12 characters were based on the dorsal sclerite (4 characters; 16 steps), ovipositor (2 characters; 13 steps), sternite VIII (1 character; 3 steps), spermathecae (3 characters; 15 steps) and spermathecal ducts (2 characters; 12 steps). We also quantified the level of homoplasy by computing the number of observed steps over the minimum number of steps for the characters (the inverse of the CI). Morphological characters related to the female reproductive tract have lower levels of homoplasy (Female: Obs./Min = 1.84) compared to non-constant third positions of the DNA barcoding gene (DNA: Obs./Min = 2.77) and the behavioral data (Behavior: Obs./Min = 2.21). (Additional file 2).
The morphology of female sperm storage organs could play an important role in post-copulatory sexual selection, influencing where the sperm is stored, how it is dispensed and whether it can be displaced. In sepsids, the main sperm storage organs are the two spermathecae and the ventral receptacle. The spermathecae are not greatly modified across the family, although there are differences in shape and size between species. Accordingly, the spermatheacae only contribute three of the 19 characters in our matrix, which account for 12.5% of the total change observed. The spermathecal ducts and ovipositor contribute even fewer changes (10% and 10.8% respectively), while the sternite VIII accounts for the least amount of change (2.5%). However, there are two features of the female reproductive tract that are evolving at a fast rate: the dorsal sclerite, which could be interacting with the male phallus and the ventral receptacle, which has been proposed as the likely the site of fertilization in several dipterans [63,64]. We believe that both structures are potential targets of post-copulatory sexual selection in Sepsidae.
With the exception of two pairs of species that are identical at the character matrix level, every other species has a unique combination of morphological characters (Table (Table2)2) and even the "identical" species differ with regard to morphological differences in characters that have continuous variation across the family. For both sister pairs [Dicranosepsis distincta &D. emiliae (Figure 14A) and Sepsis duplicata &S. secunda (Figure 14B)] the patterns of sclerotization on the dorsal sclerite differ. Although these differences are difficult to describe or code as characters with discrete states, they are nevertheless sufficiently distinct to allow for the unambiguous identification of the species. We thus find that closely related sepsid species do differ with respect to the female genitalia. In fact, based on the comparisons of the eight pairs of close relatives, all but S. duplicata and S. secunda, had higher pairwise distances in the female data than the COI barcode (χ2 test, 1 df; p = 0.034).
But did these differences in the female reproductive tract evolve quickly? In the absence of a good fossil record for Sepsidae, we can only use molecular data as a point of comparison. Most species of Diptera differ by 3-5% for the COI barcode [56,65]. Several of the closely related species-pairs that we used in our study have much lower pairwise distances: D. emiliae and D. hamata (1.49%), S. cynipsea and S. neocynipsea (1.34%), S. fulgens and S. orthocnemis (0.76%), Themira flavicoxa and T. lucida (0.69%). These low genetic distances imply that the morphological differences in the female reproductive structures must have arisen very fast. There are many studies that focus on the rapid divergence and species-specificity of male structures and emphasize the lack of stark differentiation in female structures [6,8,9,15,66,67]. Our study indicates that, the internal female genitalia in Sepsidae are not only diverse but also evolve fast and are as diagnostic for species as male genitalia and forelegs.
The dorsal sclerite evolves rapidly across the sepsid family, representing four characters in the matrix and 13.4% of all changes observed. This structure is variable even within a genus (Figure (Figure11)11) and between closely related species. In Ozerov's schematic drawing of a Themira sp., he indicated that the female reproductive tract had a 'vaginal plate', and we believe he was referring to the dorsal sclerite . However, he did not explain the functional significance of this structure. Eberhard and Huber  studied the copulation and sperm transfer in male Archisepsis and gave a detailed description as to how the male intromittent organ interacts with the female reproductive tract. They state that in addition to spiny erectable processes that anchored to the vaginal wall, the male aedaegus also had a surface densely covered with large, stiff bristles that can be pressed against the surface of a large 'vaginal sclerite' (i.e. the dorsal sclerite) . Given this description, one possible reason for the species-specific diversity in the dorsal sclerite in females, is that it has co-evolved with the species-specific male intromittent organ with which it interacts.
Sexual conflict results from the asymmetries in evolutionary interests between males and females, particularly, in relation to the control over reproduction. Both sexes accumulate traits in the form of a coevolutionary sexual arms race, with males persisting to achieve copulation using 'weapons' and females resisting their attempts with 'defenses' [68,69]. Hence, both sexes are being pulled in opposing directions resulting in the exacerbation of these antagonistic adaptations [70,71]. In sepsis, recent artificial selection experiments in Sepsis cynipsea indicate that with increasing population densities and a polyandrous system, the harm inflicted by male persistence behaviors can result in the evolution of female resistance behaviors [45,72,73]. Hence, it is possible that the highly diverse dorsal sclerites documented in this study arose as a female response or defense to prevent and/or reduce harm caused by the heavily armored male genitalia (i.e. coevolutionary morphological arms race).
Another possible explanation is that the dorsal sclerites act as structures that detect male genital stimulation (i.e. female choice) . In some tsetse flies, the males have been documented to stimulate the female internally with their aedaegus during copulation, prior to insemination [18,33-35]. In fact, in certain neotropical sepsids, males have been observed to repeatedly stimulate the females externally using their highly modified claspers to squeeze them in a rhythmic repertoire . It is thus likely that the male intromittent organs are rubbing against the dorsal scleroses and serve as courtship signals to influence post-copulatory female choice. Unfortunately, the phallus of sepsid males are poorly studied because most species can be identified based on foreleg and claspers morphology. However, future studies should test whether male intromittent organs are also species-specific and how they interact with the female internal genitalia during copulation.
The ventral receptacle displays a large amount of morphological variation across the Sepsidae, especially between genera (Figure (Figure12).12). It contributes seven of the 19 female diagnostic characters and accounts for more than half of the overall evolutionary change observed (50.8%). From a multi-chambered state in the more basal taxa like Susanomira caucasica, Saltella sphondylii and Ortalischema albitarse, the number of chambers in the ventral receptacle decreases drastically across Sepsidae. This is particularly evident within the Themira clade where the number of chambers decreases from 27 to 10. In Dicranosepsis and Sepsis, the ventral receptacle appears multi-chambered as well (Figure (Figure44,,55 and and77--1010 respectively). However, here the chambers are not clearly defined separate units. Instead, the two primary compartments are secondarily subdivided. The ventral receptacle in these is also clearly bi-lobed unlike the ones of Saltella, Susanomira or Themira. Based on the position of Dicranosepsis and Sepsis on the phylogenetic tree as well as the morphology of the internal subdivisions, we suggest that the multi-chambered ventral receptacle evolved twice (indicated by arrows in Figure Figure1212).
The ventral receptacle in Orygma luctuosum is particularly interesting (Figure (Figure6).6). Based on dissections of other acalyptrate flies (Kotrba unpublished), we believe the elongate central rod flanked by thin-walled lateral chambers of this species to be autapomorphic. Su et al. discuss conflict between morphological and molecular data in placing Ortalischema albitarse, with molecular data placing it as sister species to Orygma and morphological data placing Orygma as sister to all remaining sepsids . Given the unique ventral receptacle condition in Orygma and considering the multi-chambered ventral receptacle of Ortalischema (Figure (Figure6;6; similar to others like Themira and Saltella), our data are in line with either hypothesis and cannot be used to resolve the position of Ortalischema.
Another remarkable ventral receptacle structure is observed in Platytoxopoda and Toxopoda. The base of the receptacle in these species extends as a stalk-like tube that terminates in two strongly sclerotized chambers (Figure (Figure66 &10). These are absent in other sepsids. Interestingly, while the spermathecae of Platytoxopoda are of normal size, the spermathecae in Toxopoda are drastically reduced in size. Given these dramatic differences in the female reproductive tract, we suggest that these sister groups would be ideal for future comparative studies investigating the relative importance of the ventral receptacle versus the spermatheacae in sperm storage and fertilization. For example, some studies indicate that the evolution of female sperm storage organs drive the evolution of male sperm and sperm storage organs [22,26,75]. Hence, it would be interesting to test whether the length of the long, stalked ventral receptacle in Platytoxopoda and Toxopoda females is correlated with sperm length in the males of these species.
Considering the morphological diversity of the ventral receptacle in sepsids, the question arises as to its role in post-copulatory sexual selection. Some recent studies indicate that females are capable of biasing paternity by several means. For instance, females of the yellow dung fly Scathophaga stercoraria influence the traffic of sperm stored in the spermathecae to the point of fertilization [17,29,76] while in certain drosophilid groups females actively eject or 'dump' sperm . The specific location where fertilization takes place is still unknown for most taxa and some authors speculate that the spermathecae provide spermatozoa directly to the eggs [77,78]. Yet, a study in S. stercoraria, documented that when the egg was in the vagina, the micropyle was oriented ventrally, away from the spermathecal duct openings which open dorsally into the vaginal wall . Indeed, in many acalyptrate Diptera, the ventral receptacle is believed to be the more likely site of fertilization and some studies document the presence of spermatozoa stored in the ventral receptacle just prior to fertilization [28,79]. For instance, in ovipositing females of the Mediterranean fruit fly, Ceratitis capitata, the ventral receptacle was the first sperm storage organ to deplete, implying that it was the site where fertilization occurred , while in the Queensland fruit fly, Bactrocera tryoni, the spermathecae serve to replenish the ventral receptacle where a small number of sperm is kept for fertilizations .
Given that the ventral receptacle is the likely fertilization site in acalyptrate flies [80,81], finding great diversity in morphological structure in 41 species of Sepsidae is important. In other dipteran families like the Opomyzidae and the Tephritidae, the ventral receptacle is also multi-chambered and each chamber has been observed to house one to four spermatozoa [19,82]. In fact, in Drosophilidae, the length of the tubular ventral receptacle (also called the seminal receptacle) in females was suggested to drive the evolution of male sperm length . The general reduction in ventral receptacle chamber numbers observed in sepsids prompts future work on the possible coevolution between the number and length of stored spermatozoa and the number and volume of chambers in the ventral receptacle.
We have documented that the female genitalia are diverse across the Sepsidae, but just how fast and homoplasious are these changes? To answer these questions, we compared our female data with other character systems such as the non-constant third positions of the mitochondrial COI barcoding gene  and sepsid mating behavior . By calculating the proportion of observed changes to minimum changes, we derived convergence estimates that indicate that the female morphological characters are evolving at only approximately 2/3 the rate of molecular data (Fem: Obs./Min = 1.84; CI = 0.54). They are also not as homoplasious as the third positions (COI: Obs./Min = 2.77; CI = 0.36) or the mating behavior (Behav: Obs./Min = 2.21; CI = 0.45) (Additional file 2). However, it is important to remember that third positions of mitochondrial protein-encoding genes evolve particularly fast and so overall, the sepsid female reproductive tract can be considered a fast-evolving structure.
We document that in sepsid flies the internal female genitalia are diverse and are evolving at a much faster rate than conventionally assumed. This applies in particular to the dorsal sclerite and the ventral receptacle. The latter potentially plays a crucial role in post-copulatory sexual selection as the likely site of fertilization. With the baseline data provided in this study, experimental studies can now be designed to investigate the significance of the ventral receptacle in female choice and its possible influence on sperm competition. Also, there are an increasing number of empirical studies that document the coevolution between male and female reproductive characters. We strongly suggest that sepsids are an ideal group to study the coevolution because the female structures are now known and are diverse.
NP and MK performed the morphological preparations, the microscopic examinations and assembled the morphological character matrix. NP and RM conducted all of the phylogenetic analyses. All three authors participated in the design of the study and the writing of the manuscript. All authors have read and approved the final manuscript.
Character and character state descriptions for morphological matrix of female reproductive tract.
Table of convergence estimates for female morphology, COI barcode and sepsid mating behavior.
We would like to thank all our colleagues for their contributions to this study. In particular, we thank A.L. Ozerov for sending pinned specimens of Susanomira caucasica, Michael Balke, Martin Schaefer and Wolf Blanckenhorn for helpful intellectual contributions, and the members of the Evolutionary Biology Lab in the National University of Singapore. This study was financed by grant R-377-000-040-112 from the Ministry of Education in Singapore.