Niconiades derisor ( Mabille, 1891)
, new combination
Genomic sequencing of a syntype of
Pamphila derisor Mabille, 1891
(type locality Venezuela) from the ZMHB collection, currently in
Decinea Evans, 1955
(type species
Hesperia decinea Hewitson, 1876
) in subtribe
Hesperiina Latreille, 1809
, reveals that it originates within
Niconiades Hübner, [1821]
(type species
Niconiades xanthaphes Hübner, [1821]
) in the subtribe
Moncina A. Warren, 2008
( Fig. 11
View Figure 11
). Phenotypic assessment agrees with this placement. For instance, the syntype of
P. derisor
has brands characteristic of
Niconiades
and lacking in
Decinea
. Therefore, we propose
Niconiades derisor ( Mabille, 1891)
, new combination.
Niconiades viridis vista Evans, 1955
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is a junior subjective synonym of
Niconiades derisor ( Mabille, 1891)
Using Evans (1955), the syntype of
Pamphila derisor Mabille, 1891
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(type locality Venezuela) that we sequenced, keys to
Niconiades viridis vista Evans, 1955
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(type locality Colombia), the northern subspecies of
Thoon viridis Bell, 1930
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(type locality Bolivia). In the genomic tree,
Niconiades derisor
is indeed sister to
Niconiades viridis
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( Fig. 11
View Figure 11
), but they are not conspecific: their COI barcodes differ by 2.3% (15 bp) in the presence of definitive phenotypic differences listed by Evans (1955: 435). Therefore, we propose that
Niconiades viridis vista Evans, 1955
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is a junior subjective synonym of
Niconiades derisor ( Mabille, 1891)
.
Decinea huasteca (H. Freeman, 1969)
,
Decinea denta Evans, 1955
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and
Decinea antus (Mabille, 1895)
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are species distinct from
Decinea decinea (Hewitson, 1876)
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, and
Decinea denta pruda Evans, 1955
, new combination
Evans (1955) described genitalic differences in the presence and shape of side process of aedeagus in subspecies of
Decinea decinea (Hewitson, 1876)
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(type locality Brazil) that are more indicative of species-level differences. Our genomic tree reveals the most prominent separation of the nominotypical
D. decinea
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from other taxa ( Fig. 11
View Figure 11
), as reflected in the largest genitalic difference: long slender aedeagus process, instead of short process or no process. In COI barcodes, it translates to 5.5% (36 bp) between
D. decinea
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and
Tirynthia huasteca H. Freeman, 1969
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(type locality Mexico: San Luis Potosi). Other taxa also reveal significant differences, for example, while
Proteides antus Mabille, 1895
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(type locality Brazil:
Santa Catarina
), which is sympatric with
D. decinea
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in Southeast Brazil and lacks the aedeagus process as
T. huasteca
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, differs from the latter by 3.2% (21 bp) and the former by 5.6% (37 bp).
Decinea decinea denta Evans, 1955
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(type locality Peru: La Merced) and
Decinea denta pruda Evans, 1955
(type locality Paraguay: Sapucay) possess a short process and are more similar to each other. For these reasons, we propose that
Decinea decinea (Hewitson, 1876)
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is a monotypic species without subspecies,
Decinea huasteca (H. Freeman, 1969)
, revised status (already used as a species in several more recent publications since Miller (1992), but not in others ( Mielke 2005)),
Decinea denta Evans, 1955
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, new status, and
Decinea antus (Mabille, 1895)
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, reinstated status are species-level taxa, but
Decinea denta pruda Evans, 1955
, new combination, is a subspecies, pending further studies. The names
denta
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and pruda were published in the same work issued on the same date ( Evans 1955), and here we gave priority to the name
denta
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because of larger known distribution of this taxon that is also more common in collections.