Pseudeustrotiini
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Anterastria Sugi, 1982
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and
Pseudeustrotia Warren, 1913
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make up the noctuine tribe
Pseudeustrotiini
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, which we found to group outside of core Noctuinae with
Callyna Guenée, 1852
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;
Fracara Walker, 1856
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; and
Musothyma Meyrick, 1897
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in a poorly supported clade that also includes
Condicinae
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(BS = 23, SH = 58.6, UF = 51; Fig. 5).
Anterastria
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,
Callyna
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,
Fracara
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, and
Musothyma
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formed a clade (BS = 78, SH = 97, UF = 91), with the position of
Pseudeustrotia
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poorly supported.
Callyna
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, currently recognized in the noctuine tribe
Dypterygiini ( Holloway 2011)
has species distributed across southern Africa, southern Asia, and Australia;
Musothyma
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is a monotypic
Noctuidae
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incertae sedis genus from Australia; and
Fracara
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is a South American genus regarded to be a noctuine. It is possible
Callyna
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,
Fracara
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, and
Musothyma
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belong in
Pseudeustrotiini
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, but support values are low and these genera need to be evaluated based on additional data: both more sequence data and the morphological characters used by Beck (1996) to define
Pseudeustrotiini
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. Larval morphology does not suggest
Pseudeustrotiini
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belong in
Condicinae
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. The larva of
Pseudeustrotia carneola Warren, 1913
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has reduced prolegs on A3 and bears a broad white spiracular stripe as is common across
Condicinae
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, but the spinneret is long and dorsally grooved and the SD1 seta on A9 is hairlike, whereas most condicines have a reduced scalelike spinneret and lack a hairlike SD1 seta on A9. These spinneret and setal characteristics unite
Pseudeustrotiini
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with most Noctuinae. It is plausible that
Pseudeustrotiini
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represent a distinct subfamily, as Beck (1996) proposed, but it also plausible that they are rightfully placed in Noctuinae as our molecular data were inconclusive as to their proper placement.