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part. Halter with contrast black, elongate knob and pale yellow
stem.
Abdomen with hardly prominent gland-like structures at least
between tergites 3-4 and 4-5. Tergite 1 (Fig. 84) produced
laterally into projection bearing 3 spine-like black bristles of
different length and resting into a shallow sclerotized
excavation on tergite 2; tergite 3 with posteromarginal
spinules; tergites 4-6 with minute posteromarginal setulae;
tergite 7 with short ordinary bristles, segment 8 with short
bristles. Sternites bearing ordinary bristles becoming more
numerous and stronger toward hypopygium.
Hypopygium (Fig. 73, 74) dark brown, large. Hypandrium
with 2 strong bristles in apical part. Epandrium completely
divided. Left epandrial lamella small, fused to hypandrium,
bearing 2 long bristles in apical part. Left surstylus with upper
lobe largely divided; lower part with markedly developed
narrow surstylar comb, upper part long, slender, fused with
lower part basally. Right surstylus large, elongate oval,
lacking spines. Cerci completely fused into one large lobe,
which is subequal in size and similar in shape to right
surstylus, lacking spines, ventral and marginal bristles. Phallus
(Fig. 75) elongate, straight, strongly sclerotized.
Female. In most respects identical to male. Mid femur with
1 row of yellow ventral bristles becoming longer toward base
of femur, longest bristle longer than femur is broad. Hind
femur slender, with ordinary setation. Mid tibia lacking
spinules. Hind tibia with short posterior apical comb. Halter
with brownish knob. Abdomen lacking gland-like structures
and with unmodified tergites 1-2. Terminalia shortened.
Segment 8 normally sclerotized. Proximal margin of sternite
8 without 2 anteriorly directed rods. Apex of sternite 8
partially separated from base. Sternite 10 uniformly
sclerotized, not fused with ventroapical margin of tergite 8.
Cercus elongate oval, brownish yellow, clothed in setulae of
different length.
Measurements. – Body length 1.5-1.8 mm, wing length 1.2.-
1.3 mm.
Etymology. – In reference to a unique set of characters which
this species possesses.
Phylogenetic relationships. – The relationships of
S.
paradoxus are unresolved. In this species the female
terminalia are shortened and, thus, it appears to be more
closely related to the S. graminum and S. seeluang groups.
In S. paradoxus the upper lobe of the left surstylus is almost
completely divided that could also support this conclusion.
However, the phylogenetic value of such condition is not quite
clear at present. It should be noted that within a S. graminum
+ S. seeluang clade most of the known species have a
completely divided upper lobe of the left surstylus (S.
spinicercus, S. monospinatus, the S. graminum species
complex and the entire S. seeluang species group). Although,
the upper lobe of the left surstylus is undivided in the S.
Figs. 73-75. Stilpon paradoxus, new species, male. 73, hypopygium, ventral view, 74, same, left lateral view, 75, phallus, dorsal view; hypd
– hypandrium, rt epan lam – right epandrial lamella, rt sur – right surstylus, u lb – upper lobe of left surstylus. Scale bar: 0.1 mm.
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nubilus species complex.
S. paradoxus has the surstylar comb
and the gland-like structures on the male abdomen. However,
the first character is very homoplastic within the genus,
whereas the second one is likely to be plesiomorphous. In
the shape of the male hind femur (constricted and bent near
middle) this species resembles some North American species,
e.g. S. curvipes Melander or S. varipes Loew (Cumming &
Cooper, 1992). However, this appears to be due to the
homoplastic nature of this character rather than an evidence
of some direct relationships. Besides of the characters noted,
S. paradoxus possesses a set of unique features, which place
them aside of all other Stilpon species. In this species the
male abdominal segments 1-2 are greatly modified. Together
they appear to form a special device of uncertain functional
value. The male terminalia are also very peculiar. The cerci
are completely fused into a large lobe, which is strictly similar
in size and shape to the right surstylus. The right epandrial
lamella is small and it is distinctly smaller than the left
epandrial lamella (in Tachydromiinae normally vise versa).
The phallus is elongate, straight, thick and strongly sclerotized
(elongate, hair-like and curved in the S. divergens species
group, very short and rather weakly sclerotized in the S.
graminum and
S. seeluang groups). Unfortunately, at the
present state of our knowledge of the genus, almost all these
characters are usefulness for the discussion some relationships
of this species. Some of them are insufficiently studied in
the Drapetini on the whole (e.g., aedeagal complex). The
phylogenetic value of others may be clarified when new un-
described species are discovered.
Distribution and seasonal occurrence. – Thailand. Known
from one locality only. Records are from the first decade of
February to late May. Collected on riverbanks in gallery
forest.
Stilpon yai, new species
(Figs. 76-79)
Material examined. – Holotype - male,
THAILAND: Loei
Province, Na Haeo, Chang Tok, riverbed, sample n
°
21047, 9
May.2001, coll. P. Grootaert (coll. RBINS).
Diagnosis. – Readily distinguished
from other species known
from Oriental region by its large size, veins R4+5 and M
parallel and straight in apical part, male mid femur with 3
black antero- and 2 longer posteroventral spines in basal half.
Description. – Male. Head black in ground-colour, with
minute anterior ocellars, somewhat longer posterior ocellars
and long inner verticals. Antenna and palpus brownish yellow.
Postpedicel nearly 1.5 times longer than wide. Style nearly
8 times longer than postpedicel.
Figs. 76-79. Stilpon yai, new species, male. 76, mid leg, anterior view, 77, hypopygium, ventral view, 78, upper lobe of left surstylus, dorsal
view, 79, right epandrial lamella and right surstylus, dorsal view. Scale bar: 0.1 mm.