Engelimyia
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clade
The
Engelimyia
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clade (clade 64) is composed of the genera
Engelimyia
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and
Tulaeopoda
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, which are consistently recovered in a sister-group relationship. The genus
Tulaeopoda
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had not yet been included in a phylogenetic analysis. Lopes (1969a) included it in the tribe
Sarcophagini
and suggested it is most closely related to
Peckia
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( Lopes, 1941b, 1975d, 1983). In the last decade, species of
Engelimyia
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were included in molecular and morphological phylogenetic analyses, although without a conclusive result on the phylogenetic position of this genus. Pape & Mello-Patiu (2006) did not propose any genus or group of genera as a candidate sister group of
Engelimyia
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, but they discussed and rejected any possible phylogenetic relationship of this genus to
Peckia
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. However, Giroux et al. (2010) found
Engelimyia
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as sister to (
Peckia
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+ (
Sarcodexia lambens
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+
Titanogrypa
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)).
Engelimyia
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has been included in two molecular analyses, where it emerged either in a trichotomy with
Boettcheria
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and
Tricharaea ( Kutty et al., 2010)
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, or as sister to
Boettcheria
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alone ( Piwczyński et al., 2014).
The
Engelimyia
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clade has strong branch support in our analysis.
Engelimyia
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and
Tulaeopoda
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share ten autapomorphies: (1) male hind femur curved, (2) male abdominal ST3 with one or two patches of dense, erect, black setae, (3) male abdominal ST4 with two patches of dense, erect, black setae, (4) male ST5 with a small pad of stubby setae medially on the inner margin of cleft, (5) cercal prong gradually swollen with a knob-like apex ( Fig. 44H
View Figure 44
), (6) cercal prong with dorso-lateral keels, (7) cercal prong with a lateral tuft of long setae, (8) paraphallic tube as long as broad ( Figs 22A
View Figure 22
, 27H
View Figure 27
), (9) stylar lateral plates present ( Fig. 22A
View Figure 22
) and (10) juxta globose, spinose and denticulated ( Figs 22A, B
View Figure 22
, 27H–J
View Figure 27
, 34A
View Figure 34
). Pape (1996) already listed character state 1 in his diagnosis of
Engelimyia
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, and he also used a similar interpretation of character state 7 as presented here but restricted it to the diagnosis of
Tulaeopoda
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. Character states 4–8, as presented here or slightly modified, are included in the diagnosis of
Engelimyia
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by Pape & Mello-Patiu (2006). The present study confirms the presence of stylar lateral plates (character state 9) in both
Engelimyia
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and
Tulaeopoda
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. Also, the juxta of
Engelimyia
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(character state 10) is reinterpreted and homologized with a globose, spinose and denticulated structure, while in previous works ( Pape & Mello-Patiu, 2006; Giroux et al., 2010) the juxta was homologized with a sclerotized and smooth bifid structure ( Fig. 22C
View Figure 22
), which is here considered a structure evolved de novo in
Engelimyia
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.
Pape & Mello-Patiu (2006) defined
Engelimyia
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and discussed its monophyly. Many of the diagnostic character states listed by these authors are reinterpreted here, but
Engelimyia
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still emerges as monophyletic in our phylogeny. In a previous phylogenetic study ( Buenaventura & Pape, 2015), we provided new interpretations of the uniquely shaped median stylus and capitis of
Engelimyia
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( Fig. 22A, B
View Figure 22
), as well as the description of acrophallic structures such as the stylar membranous lobes and stylar lateral plates ( Fig. 22A
View Figure 22
). As outlined above, only the stylar membranous lobes are autapomorphic for
Engelimyia
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, as well as male abdominal ST3 with a single patch of dense, erect, black setae.
Two autapomorphies support
Tulaeopoda
: the posterior surface of the male hind trochanter with a postero-median pad of short setae (position as no. 6 in Fig. 45
View Figure 45
) and male abdominal ST3 with two patches of dense, erect, black setae. Contrary to what was suggested by Pape (1996), species of
Tulaeopoda
possess well-developed, tubular lateral styli ( Fig. 27I, J
View Figure 27
).