MEM INST OSWALDO CRUZ, RIO DE JANEIRO, 107(2) March 2012
PAGES: 178-185 DOI: 10.1590/S0074-02762012000200005 Full paper
The phylogeny of Simulium (Chirostilbia) (Diptera: Simuliidae) and perspectives on the systematics of the genus in the Neotropical Region 

Leonardo Henrique Gil-AzevedoI, II, +; Sixto CoscarónIII; Marilza Maia-HerzogII

IDepartamento de Zoologia, Instituto de Biologia, Universidade do Estado do Rio de Janeiro, Rua São Francisco Xavier 524, 20550-013 Rio de Janeiro, RJ, Brasil
IILaboratório de Simulídeos e Oncocercose, Instituto Oswaldo Cruz-Fiocruz, Rio de Janeiro, RJ, Brasil
IIIFacultad de Ciencias Naturales y Museo, La Plata, Buenos Aires, Argentina

Abstract

Recently, knowledge of Neotropical Simuliidae has been accumulating quickly. However, information about supra-specific relationships is scarce and diagnoses of Simulium subgenera are unsatisfactory. To investigate the relationships among Simulium (Chirostilbia) species and test the subgenus monophyly, we performed a cladistic analysis. The ingroup included all species of this subgenus and the outgroup included representatives of the 17 species groups of Neotropical Simulium and three Holarctic species. The study was based on a data matrix with 31 terminal taxa and 45 morphological characteristics of adult, pupa and larva. The phylogenetic analysis under equal weights resulted in eight most-parsimonious trees (length = 178, consistency index = 34, retention index = 67). The monophyly of the S. (Chirostilbia) was not supported in our analysis. The Simulium subpallidum species group was closer to Simulium (Psilopelmia) and Simulium (Ectemnaspis) than to the Simulium pertinax species group. Additionally, we describe the three-dimensional shape of the terminalia of male and female of Simulium (Chirostilbia) for the first time and provide comments about the taxonomic problems involving some species of the subgenus: Simulium acarayense, Simulium papaveroi, S. pertinax, Simulium serranum, Simulium striginotum and S. subpallidum

Systematic knowledge of the Neotropical Simuliidae has been accumulating quickly and there are 351 valid Neotropical species (Coscarón et al. 2008, Adler & Crosskey 2010, Hamada et al. 2010). Over the past 10 years, 67 taxonomic papers involving 20 researchers, as well as two extensive manuals, have been published (Coscarón & Coscarón-Arias 2007, Shelley et al. 2010), resulting in the description of 18 new species (Adler & Crosskey 2010, Hamada et al. 2010). Consequently, the Neotropical black fly became relatively well known and, unlike most of the other Neotropical animal taxa, a basic lack of data no longer is an issue (Rocha & Boerger 2009).

Eleven subgenera of Simulium Latreille, 1802 have been found in the Neotropical Region (Adler & Crosskey 2010). Most of the species in these subgenera are well described and well represented in institutional collections. However, knowledge of supraspecific group relationships is very scarce and subgenera diagnoses are unsatisfactory. In addition, there are problems in the delimitation of the identity of some species. As a result of these problems, divergent systematic arrangements exist in the literature (Py-Daniel & Sampaio 1995, Coscarón et al. 2008, Adler & Crosskey 2010, Shelley et al. 2010) and loose synonymies of species are often proposed, which tend to appear and disappear in the literature.

In the literature, all systematic decisions were made exclusively based on personal opinions, without any clear methodology or hypothesis; as a result, one cannot rationally reject or accept the changes proposed. There have been a few morphological phylogeny studies, but they have not targeted major subjects such as the monophyly of subgenera, the relationship amongst the subgenera or the species identity (e.g., Coscarón & Coscarón-Arias 1997, Strieder & Py-Daniel 2002). In addition, there are limited molecular, cytogenetic and morphometric works dealing with Neotropical taxa (e.g., Coscarón-Arias 1998, Scarpassa & Hamada 2003, Hamada et al. 2008, 2010). Therefore, the real problem underlying current Neotropical Simuliidae systematics is the organisation of the massive amount of data produced over the years.

Simulium (Chirostilbia) Enderlein, 1921 is a good case study because it is a group endemic to the Neotropics and has remained taxonomically stable. For example, no researchers have ever questioned the monophyly of the group; however, as with the other subgenera, the position of the group within Simulium is unknown and the diagnoses made for this group are too broad and are inadequate to clearly identify the subgenus (Coscarón 1981, Coscarón & Coscarón-Arias 2007, Hernandez et al. 2008).

In the present study, a cladistic analysis was performed to test the monophyly of Simulium (Chirostilbia) and to evaluate the phylogenetic structure within the subgenus. We also provide comments about the taxonomic problems of some species of Simulium (Chirostilbia).

Historical background - Chirostilbia was created by Enderlein (1921a: 199) as a genus, with Chirostilbia flavi-femur Enderlein, 1921, as the type species and was fully described by Enderlein in a different publication (1921b: 79). Subsequently, Chirostilbia was considered a subgenus of Simulium (Pinto 1932) and Lane and Porto (1939) considered Simulium flavifemur as a synonym for Simulium pertinax Kollar, 1832. Coscarón (1981) established the subgenus, which contained five species. Coscarón (1982) proposed the Simulium subpallidum species group with three species later included in Simulium (Chirostilbia) (Coscarón 1987). He considered Simulium (Chirostilbia) to have two species groups: S. pertinax and S. subpallidum. Coscarón and Coscarón-Arias (1997) performed the only phylogenetic analysis of the subgenus, with 18 characters, 12 taxa in the ingroup and Simulium (Inaequalium) as the outgroup. Coscarón et al. (2008) considered 15 species in Simulium (Chirostilbia), 12 in S. pertinax and three in the S. subpallidum species group. The division into these species groups was contested by Hernández et al. (2008), who do not consider Coscarón's characters valid.

 

MATERIALS AND METHODS

Terminal taxa and specimens - The ingroup taxa consisted of all the species of Simulium (Chirostilbia) except for Simulium striginotum (Enderlein, 1933), which is known only by a female, for a total of 14 terminal taxa. The chosen outgroups were as follows: Metacnephia saileri (Stone, 1952), representatives of two Simulium subgenera from the Holarctic Region, Simulium (Hellichiella) nebulosum Currie & Adler, 1986 and Simulium (Eusimulium) aureum Fries, 1824 and the 17 species groups of Neotropical Simulium recognised by Adler and Crosskey (2010).

The specimens studied herein are deposited in the following institutions: the Museo de La Plata (MLP) (Argentina), the Museu de Zoologia de São Paulo (Brazil), the Faculdade de Saúde Pública da Universidade de São Paulo (Brazil), the Coleção Histórica de Adolpho Lutz, Instituto Oswaldo Cruz (Brazil), the Coleção do Laboratório de Simulídeos e Oncocercose, Instituto Oswaldo Cruz (Brazil), the Instituto Nacional de Pesquisa da Amazônia (Brazil) and the Royal Ontario Museum (Canada). Whenever possible, we examined specimens of three developmental stages (larva, pupa and adult). The techniques used to prepare and observe the specimens and specimen-related material were previously described in Gil-Azevedo et al. (2005). Additionally, the preparations involved and the techniques used to observe the three-dimensional shape of the terminalia in a drop of glycerin on a depression slide were described in Adler et al. (2004).

Terminology and characters - We followed the morphological terminology of Adler et al. (2004), with the addition of terms from Gil-Azevedo and Maia-Herzog (2007). Based on an extensive morphological study, we identified the characters and proposed hypotheses of primary homology (Pinna 1991) (Supplementary data). The logic employed in the preparation of characters followed Sereno (2007). We codified these hypotheses in a data matrix using the program Mesquite (Maddison et al. 1997, Maddison & Maddison 2007) (Supplementary data). Characters were preferentially coded reductively (Wilkinson 1995) and were treated as unordered (Fitch 1971). When two or more states of a character were found in one terminal taxon, the character was treated as polymorphic and both states were coded in the matrix.

Phylogenetic analyses - The dataset was analysed with maximum parsimony equal weights. The searches were carried out through heuristic algorithms. The parameters of the search were as follows: 3,000 replications and Tree bisection and reconnection with 1,000 trees saved per replication. The branch support was evaluated by bootstrap (Felsenstein 1985) with 5,000 replications by decay index (Bremer 1994), through the search of suboptimal trees and by a sensitivity analysis using analyses under implied weights (Goloboff et al. 2008b) (k = 3, 6, 10, 15, 20, 25). We used the TNT program for all searches (Goloboff et al. 2008a). Character optimisation, mapping and comparisons among the obtained trees were carried out with WinClada (Nixon 2002).

 

RESULTS

The data matrix was composed of 34 terminal taxa and 45 characters obtained from adult (25), pupa (12) and larva specimens of the last instar (8) (Supplementary data). The list of characters used in this analysis is given in Supplementary data.

The phylogenetic analysis under equal weights resulted in eight most-parsimonious trees with 178 steps, consistency index = 0.34 and retention index = 0.67 (Fig. 1, Table I). The obtained hypothesis indicates that Simulium (Chirostilbia) is not a monophyletic group because the S. subpallidum species group is closer to Simulium (Psilopelmia) Enderlein, 1934 + Simulium (Ectemnaspis) Enderlein, 1934, than to the S. pertinax species-group (Fig. 1). In spite of the low support from the bootstrap analysis and the decay index, the strict consensus tree has a good resolution and the clades are also found in the implied weights analyses (Fig. 1, Table II). We chose one of the shortest trees for character distribution and optimisation (Fig. 2).

 

 

 

 

Description of the terminalia of Simulium (Chirostilbia) based on a three-dimensional view - Female terminalia (Fig. 3): the hypogynial valves are small and subtriangular with slightly divergent external margins. The anal lobe is long and subtriangular, approximately 2.5-fold longer than wide in the lateral view. The internal sides of the anal lobes are concave and facing each other, resembling a pair of long spoons. Therefore, when the anal lobe is fixated in a slide, it may either be wider and less curved or narrower and more curved, depending on whether the dorsal axis of the anal lobe is central or lateral, respectively (Hernandez et al. 2007, Figs 118, 121, respectively). The anal lobe is approximately three-fold longer than the cerci. The cerci are hemispheric and distinctly longer than wide in the lateral view. The internal sides of the cerci are concave and face each other like brackets. The genital fork stem is as long as the lateral arms and the spermatheca are oval; male terminalia (Fig. 4): the gonocoxites are subtrapezoidal to subquadrangular. The gonostyles are subtriangular and curved towards the aedeagus. In the S. subpallidum species group and Simulium jefersoni Hamada et al., 2006 the height of the gonostyle is distinctly longer than the base, whereas in the others the height and the base are similar sizes. The apical spur of the gonostyle is absent, but there is a sclerotized longitudinal ridge along the external border. The longitudinal ridge likely has the same function as the apical spur in other groups. The ventral plate is wider than it is long, with little curvature seen in profile, and is not very narrow apically. The median sclerite is widened with a strong median concavity. A dorsal sclerite is present as a sclerotized thin line. The paramere is elongated with developed teeth and connected to the apex of the ventral plate arms.

 

 

 

 

Below we give some remarks on some taxonomic species of Simulium (Chirostilbia).

The S. pertinax Kollar, 1832 has a complex taxonomic history, as explained in Shelley et al. (1984), but is not particularly complicated taxonomically, as suggested by Hernandez et al. (2008). There are six junior synonyms of S. pertinax, but these are easily explained. This species has a continental distribution and is a vicious human biter; as a result, it is easy to find and has been collected by different and isolated authors, who went on to describe it as a new species. S. pertinax is homogeneous based on morphological (Gil-Azevedo et al. 2004) and cytological (Campos et al. 1996, 2001) data and there is no reference in the literature to delimitation problems for this species. Such problems are common for other Simulium species (e.g., S. subpallidum Lutz, 1910 and Simulium incrustatum Lutz, 1910). Hernandez et al. (2008) recorded this species in Bolivia (north of Santa Cruz; 16.V.1989, JJ McGrande coll.) based only on two biting females. We did not consider this a valid occurrence because those females could have been from any Simulium (Chirostilbia) species and we prefer to wait until someone collects additional exemplars associated with pupae to confirm this occurrence.

Simulium serranum Coscarón, 1981 - Originally, Coscarón (1981) named this species S. serranus, but Simulium is neutral in gender and serranus is an adjective in the masculine form. According to the International Code of Zoological Nomenclature, the species-group name should agree in gender with the genus (ICZN 1999: 31.2); thus, the corrected name is now S. serranum.

Hernandez et al. (2007) observed the holotype of S. striginotum (Enderlein, 1933) [1 female, Bolivia, Department of La Paz, Mapiri, Sarampione (14.II.1903)] and synonymised this species with Simulium spinibranchium based on the scutum colouration, morphology of the cibarium, nudiocular area, wing setation, leg colouration and the structure of the genitalia, especially the cercus and anal lobe. We do not accept this synonymy because the colouration of exemplars collected over a century ago is not reliable. In addition, wing setation and the structures of genitalia are very similar in all Simulium (Chirostilbia) species. Moreover, the Department of La Paz is located in the Bolivian Altiplano, at a high altitude and very far from locations associated with any records of Simulium (Chirostilbia) species; therefore, this is likely a valid separate species. Although we agree with Hernandez et al. (2007) that this species is most likely within the S. pertinax species group of S. (Chirostilbia), it is necessary to collect fresh material of all stages at the type-locality to define the identity of the species properly.

Hernandez et al. (2007) synonymised Simulium acarayense Coscarón & Wygodzinsky, 1972 with S. subpallidum and we agree that there is only one distinctive character between both species, the scutum colouration, but the species also differ in pupal and larval continuous characters that are related to environmental variables: the length of the pupal gill, the number of rays in the larval cephalic fan, the number of hook rows of the larval anal ring and the number of lobes in the larval rectal papillae. We accept this synonymy for now, but future works based on morphometry, molecular or cytological data are necessary to properly define the identity of the species.

Hernandez et al. (2008) indicate that Simulium papaveroi Coscarón, 1982 is morphologically similar to Simulium dekeyseri Shelley & Py-Daniel, 1981 and S. serranum based only on a few female and pupal characters, mainly scutum colouration, female terminalia and pupal gills. These characters are very similar in all species of

Simulium (Chirostilbia) sensu lato and likely for this reason, these authors did not recognise the S. subpallidum species group. However, a careful observation of the specimen characters, including male terminalia, pupal cocoons and larval heads, indicates that this species is closer to S. subpallidum.

 

DISCUSSION

The monophyly of the Simulium (Chirostilbia) was not supported in our analysis because the S. subpallidum species group was closer to Simulium (Psilopelmia) Enderlein, 1934 + Simulium (Ectemnaspis) Enderlein, 1934 than to the S. pertinax species group (Figs 1, 2). These analytical results may explain the weak diagnoses of the subgenus throughout the literature (e.g., Coscarón 1981, 1991, Hernandez et al. 2008). These results also indicate the importance of performing cladistic analyses in taxa reviews, especially when proposing systematic changes. Based on our data, we see two possibilities: restricting Simulium (Chirostilbia) to the S. pertinax species group and creating a new subgenus for the S. subpallidum species group, or including and synonymising Simulium (Psilopelmia) and Simulium (Ectemnaspis) with Simulium (Chirostilbia). We believe the second option is preferable, but our analyses do not have enough bootstrap or Bremer support to make us comfortable proposing these changes at this time. A more complete analysis of Simulium is necessary before implementing a deeper rearrangement of Simulium subgenera.

The division of S. (Chirostilbia) into species groups, as proposed by Coscarón (1991), was contested by Hernandez et al. (2008). The latter authors argue that "the species do not clearly fit into groups because of the variation and overlap of morphological characters, especially the colouration of the thorax and the form of the male gonostyle" (Hernandez et al. 2008). We agree that these two characters do not justify the species groups; however, Hernandez et al. (2008) ignore other characters, such as sub-basal claw teeth, cocoon shape and larval head characters that differentiate the species groups (Table II). In fact, our analyses indicate that the two groups are monophyletic and may not be sister groups (Figs 1, 2).

The S. pertinax species group was recovered in all of our analyses. In our basal branches, the resolution is poor and the relationship amongst S. dekeyseri, S. serranum, S. spinibranchium and the major branch requires further investigation. However, the resolution within the major branch is clear. The major branch presents, as synapomorphies, female scutum patterns with blurred stripes, a male gonostyle more than two-thirds the length of the gonocoxite and larvae with 8 + 8 hypostomal setae or more. S. pertinax is in the base of the major branch opposed to the group formed by boot-shaped cocoon species (the only exception is Simulium bifenestratum Hamada & Pepinelli, 2004 that has a highly derivative cocoon and was treated as inapplicable for this character). Inside the boot-shaped cocoon clade, there are two branches: (Simulium obesum Vulcano, 1959 (Simulium friedlanderi Py-Daniel, 1987 + S. jefersoni)) and (Simulium empascae Py-Daniel, Souza & Caldas, 1988 (S. bifenestratum (Simulium distinctum Lutz, 1910 + Simulium riograndense Py-Daniel, Souza & Caldas, 1988))). The synapomorphies of these branches are as follows: the larvae with positive apoteme and cocoon fabric with visible thick threads are synapomorphic with the first branch and the pupa with cephalic trichomes that are small and thin and are synapomorphic with the second. In addition, the clade (S. bifenestratum (S. distinctum + S. riograndense)) is well defined and presents three synapomorphies: female with the distal apex of the anal lobe pointed, pupal gill with 10 filaments and gill filaments arrangement two-dimensionally and forming an almost complete circle.

Our tree is similar to the tree found by Coscarón and Coscarón-Arias (1997). Both trees recovered the S. pertinax and S. subpallidum species-groups, but the 1997 paper did not test the Simulium (Chirostilbia) monophyly because only one outgroup, Simulium (Inaequalium) Coscarón & Wygodzinsky, 1984, was used. In addition, the 1997 tree indicates two distinct clades in the S. pertinax species group: S. dekeyseri (as Simulium laneportoi Vargas, 1941) + S. pertinax + S. serranum + S. spinibranchium, and S. distinctum + S. empascae + S. friedlanderi + S. obesum + S. riograndense. However, our tree presents the first group as paraphyletic and the second with more resolution. These differences may result from the inclusion of more characters (45 against 18 for the 1997 tree) and the inclusion of the more recently described taxa, S. bifenestratum and S. jefersoni.

The representatives of the Neotropical Simulium subgenera were used here to test the monophyly of Simulium (Chirostilbia). However, the trees obtained provide insights about the relationships among these subgenera. Some groups were formed with large numbers of non-ambiguous synapomorphies and were recovered in implied weights analyses. We comment on these clades following.

Simulium (Hearlea) + Simulium (Hemicnetha) + Simulium (Trichodagmia) - Simulium (Hemicnetha) Enderlein, 1934 and Simulium (Hearlea) Vargas, Martínez Palacios & Díaz Nájera, 1946, were synonymised by Adler et al. (2004) based on a phylogeny of Nearctic simuliids. Shelley et al. (2010) proposed the synonymy of both with Simulium (Trichodagmia) Enderlein, 1934, based on Enderlein's papers (1934a, b, 1936) but did not discuss more modern definitions of the subgenera (e.g., Coscarón 1991, Miranda-Esquivel 2001). The group was recovered in our phylogeny with five synapomorphies (Fig. 2) and it is likely that these subgenera are closely related. Moreover, some Afrotropical Simulium subgenera, such as Simulium (Anasolen) Enderlein, 1930, Simulium (Freemanellum) Crosskey, 1969, and Simulium (Xenosimulium) Crosskey, 1969 are likely also related to this clade (Miranda-Esquivel & Coscarón 2001) and an analysis with all Simulium subgenera is necessary to test these hypotheses.

Simulium (Inaequalium) + Simulium (Psaroniocompsa) - Shelley et al. (2010) proposed the synonymy of Simulium (Psaroniocompsa) Enderlein, 1934 and Simulium (Inaequalium) based on their personal opinion concerning the characters of the original diagnosis of Simulium (Inaequalium) ("... none is considered by us to be of subgeneric value."). Simulium (Inaequalium) and Simulium (Psaroniocompsa) are sister groups, as proposed by Coscarón and Wygodzinsky (1984), and were recovered here with three synapomorphies (Fig. 2). Both subgenera are very distinct and have an easily recognisable morphology. We also disagree that there are "good or bad" characters for specific hierarchical categories. Therefore, we think that this synonymy is unnecessary.

Simulium (Notolepria) + [Simulium (Psilopelmia) + Simulium (Ectem-naspis) + Simulium (Chirostilbia)] - The relationship amongst these subgenera has not been proposed before and the group has four synapomorphies (Fig. 2). The clade Simulium (Chirostilbia) + Simulium (Psilopelmia) + Simulium (Ectemnaspis) presents four synapomorphies (Fig. 2) and brings back a forgotten issue in the Neotropical black fly history. Stone (1963) proposed the synonymy of Chirostilbia and Ectemnaspis based on similarities of female terminalia of the type species; Wygodzinsky (1971) argued that the species were quite different when comparing male and pupa but stressed that the "Ectemnaspis-Chirostilbia complex", as he denominated it, needed further investigation. We agree with that suggestion.

In the literature, there is no consensus regarding the limits of Simulium (Psilopelmia) and Simulium (Ectemnaspis) (Coscarón et al. 2008, Adler & Crosskey 2010) and Shelley et al. (2010) proposed the synonymy of both based on that. In our phylogeny, these species groups were recovered as a monophyletic group with four synapomorphies and Simulium (Psilopelmia) was paraphyletic without Simulium (Ectemnaspis), corroborating their synonymy. However, it is still necessary to examine the relationship between the group and Simulium (Psilozia) Enderlein, 1936 (Adler et al. 2004).

Some characters that have been traditionally used in the systematic classification of Neotropical simuliids were tested in the present analysis, including the scutum colouration of adults, the number of branches of pupal trichomes and the number of hypostomal setae of larvae. The phylogenetic signal of these characters was weak, with low consistency and retention indexes. Thus, these characters are not reliable for defining groups and require further investigation.

Many systematic problems in the Neotropical Simulium species are still unsolved and the traditional morphology seems to be inconclusive in some respects. A broad approach is important, using chromosomal, molecular biology and morphology data, as has been shown in the studies of Nearctic Simulium (Adler et al. 2004). Studies using these techniques are incipient in Neotropical Region and this needs to change. At the same time, the morphological studies in the region have not been fully explored. For example, in the present work, a three-dimensional view of a Neotropical Simuliidae terminalia was described for the first time, a character that has been used for Nearctic fauna since the 1970s. In addition, studies using scanning electron microscopy and/or morphometry in the region are rare.

Whatever the tool used, systematic changes must be grounded in a methodology, whether cladistic or probabilistic. Systematics without a basic methodology and based on key features or personal opinion only lead us into a vicious circle. Such systematics proposals are not based on a clear method and lack hypotheses. Therefore, they cannot be rejected or corroborated by other researchers and need to be avoided.

 

ACKNOWLEDGEMENTS

To Dr Neusa Hamada and Dr Victor Py-Daniel (INPA) and Douglas Currie (ROM), that kindly permitted access to their respective collections and donated additional material, to Dr Amanda Mendes (MN-UFRJ) and the two anonymous rewires that contributed many thoughtful suggestions that improved this work.

 

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Received 9 May 2011
Accepted 29 November 2011
Financial support: CNPq

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