New species of Leleja (Orthoptera: Gryllinae; Gryllini) with first female description for the genus
Author
Tan, Ming Kai
Author
Artchawakom, Taksin
text
Zootaxa
2017
4236
3
592
600
journal article
36446
10.11646/zootaxa.4236.3.12
ef210615-3926-461d-8701-229d9791e272
1175-5326
322332
1733E55C-DE2E-4DE0-99DC-421CB2A7894F
Leleja khao
,
new species
(
Figs. 2–5
)
Material
examined.
Holotype
(male):
Thailand
,
Nakhon Ratchasima
,
Sakaerat Environmental Research Station
, dry dipterocarp forest,
N14.50914
,
E101.93811
, 355.7 ±
5.3 m
, on ground,
30 June 2014
, 2110 hours, coll.
M. K. Tan
,
H. Yeo
&
S. T. Toh
(
SERS
.14.141) (
ZRC
).
Paratype
:
Thailand
, same locality, dry dipterocarp forest:
1 female
(
SERS
.14.83),
N14.50921
,
E101.93700
, 398.3 ± 6.0m, on grassy patch,
26 June 2014
, 2228 hours
; 1 male (SERS.14.144) and 1 female (SERS.14.145), N14.50944, E101.93826, 353.2 ±
4.8 m
, on ground,
30 June 2014
, 2148 hours; all coll. M. K. Tan, H. Yeo & S. T. Toh (all ZRC).
Diagnosis.
Posteromedial process of epiphallus distinctly protruding to produce rectangular lobe; proximal part of medial lobe of ectoparamere narrow, elongated slender process with acute apex, pointing posteriorly and touching each other at apex, with hairs at apex.
Comparison with congeners.
This new species differs from
Leleja arkadiyi
by male genitalia: transverse bridge of epiphallus narrower and with a few long hairs along posterior margin (wider in
L. arkadiyi
); anterolateral apodemes of epiphallus very short, not reaching anterior end of endoparamere (longer and surpassing anterior end of endoparamere in
L. arkadiyi
); posteromedial process of epiphallus distinctly protruding to produce rectangular lobe (less distinctly protruding in
L. arkadiyi
); ectoparamere with basal part stouter; proximal part of medial lobe of ectoparamere narrow, elongated slender process with acute apex (instead of a short lobe with obtuse apex in
L. arkadiyi
), pointing posteriorly and touching each other at apex, with hairs at apex (not touching each other and without hair at apex in
L. arkadiyi
); and ramus shorter.
The two species also differ in their distribution and natural habitat:
Leleja arkadiyi
from Nong Bun Nak at about
200 m
a.s.l. (part of the
Khorat
plateau) and the new species from Sakaerat at about
350 m
a.s.l. (part of the Dong Phaya Yen mountains and Sankamphaeng range) (
Fig. 1
). Further sampling in the region is needed to ascertain if they are allopatric or sympatric species.
Description.
Habitus typical for the genus (
Fig. 2
A). General shape rather stout. Head very large, 1.2 times longer than pronotum, clypeal suture to dorsum of head about as tall or slightly taller than pronotal lateral lobe; distinctly globular (
Fig. 3
A). Fastigium verticis and fastigium frontis fused, forming a frontal rostrum; inflated in profile (
Fig. 3
A). Ocelli placed in a strongly transverse triangle; medial ocellus at the top of the frontal rostrum; lateral ocellus dorsad of scapus (
Fig. 3
B). Frons below medial ocellus to above clypeal suture smooth and inflated; clypeal suture distinct and transverse, ending above mandible and at anterior margin of eye (
Fig. 3
B). Mandible stout; labrum large, wider and longer than clypeus (
Fig. 3
B). Maxillary palps slender, apical (fifth) segment longest, followed by third and then fourth (subapical) segments; basal (first) and second segments stout; apical segment with posterior margin oblique (
Fig. 3
A). Pronotal dorsal disc distinctly wider than long, with lateral margins narrowing posteriorly, anterior margin straight, posterior margin slightly concave; longitudinal suture distinct (
Fig. 2
A). Pronotal lateral lobe taller than long (
Fig. 3
A). Legs rather short and pubescent. Anterior and middle legs with some thicker and spine-like hairs dorsally; first and second tarsal segments with stout hairs arranged in rows ventrally. Anterior tibia with one outer apical spine and two longer inner apical spines; a large, oblong external tympanum, internal tympanum absent. Middle tibia with two outer and two longer inner apical spines; dorsal ones much shorter than ventral ones. Posterior femur strongly dilated, slightly narrowing towards apex. Posterior tibia with 5 internal and 6 external subapical spurs; 3 internal and 3 external apical spurs. Posterior tarsus with 5 internal and 7 external dorsal spines.
Male. Tegmen truncated, reaching 3rd abdominal tergite, the stridulatory apparatus functional (
Fig. 3
C). Stridulatory area of tegmen with 2 sinuous oblique veins (= harp veins) and 2 broadly rounded cord veins; mirror broader than long, pyriform, without dividing vein (
Fig. 3
C). Lateral field of tegmen with 7-8 longitudinal veins (= Sc branches). Supra-anal plate longer than broad; plate basal half rectangular and transverse with a longitudinal furrow in middle, forming lateral lobe at the posterior angle; apical half depressed in the middle, longer than wide with apical margin truncated (
Fig. 3
D). Subgenital plate simple, elongated and tapering into subacute apex.
Phallus (
Figs. 3
E–I):
Epiphallus
H-shaped;
transverse bridge
narrow and with few long hairs along posterior margin (
Figs. 3
E, 3F);
anterolateral apodemes of epiphallus
very short, not reaching anterior end of
endoparamere
(
Figs. 3
E, 3F);
posterolateral process
elongated, posterior half of process tapers into an obtuse apex with some short hairs in profile, apex of process bent internally in dorsal/ ventral views (
Figs. 3
E–H), in profile curved dorsally and separated from the epiphallus bridge by deep dorsal notch (
Fig.
3
I);
posteromedial process
(not to be confused with median posteroventral projection) very stout, dorsad of posterolateral process (
Fig. 3
E), in profile distinctly protruding to produce rectangular lobe with dense long hairs along posterior margin (
Fig.
3
I).
Ectoparamere
with basal (= anterior) part stout and stick-like, distal (= posterior) part broadly rounded (
Fig. 3
G);
distal part of medial lobe of ectoparamere
vertical, flattened and elongated, slightly membranous and apex truncated;
proximal part of medial lobe of ectoparamere
narrow (much narrower than distal part in profile), curved inwards and posteriorly to produce elongated slender process with acute apex; rachis pointing posteriorly and touching each other at apex, with hairs at apex, valve between process distinctly long (
Figs. 3
E–H).
Endoparamere
slender, forming an M-shaped and fused at the end (
Figs. 3
F, 3H).
Ramus
relatively stouter (
Figs. 3
F, 3H).
Virga
lost during dissection.
FIGURE 2.
Leleja khao
sp. n.
: male (A) and female (B) adult habitus in dorsal view. Scale bars: 10 mm.
FIGURE 3.
Leleja khao
sp. n.
male: head and pronotum in profile (A); head in frontal view (B); tegmen in dorsal view (C); abdominal apex in dorsal view (D); phallus in postero-dorsal (E), dorsal (F), ventral (G, H) views and profile (I). Scale bars: 2 mm (A), 1 mm (B–D); 0.5 mm (F, H, I).
FIGURE 4.
Leleja khao
sp. n.
female: head and pronotum in profile (A), tegmen in dorsal view (B); abdominal apex in dorsal view (C); apex of ovipositor in profile (D). Scale bars: 2 mm (A), 1 mm (B, C), 0.5 mm (D).
Female. Habitus larger than male (
Fig. 2
B). Head large, but not distinctly longer than pronotum (
Fig. 4
A). Pronotal dorsal disc with lateral margins feebly narrowing posteriorly; anterior margin feebly emarginated in middle, posterior margin substraight (
Fig. 2
B); pronotal lateral lobe longer than tall (
Fig. 4
A). Tegmen truncate posteriorly, reaching middle of 2nd tergite, touching each other only at basal area; dorsal and lateral fields with 6-7 longitudinal veins each (
Figs. 4
A, 4B). Supra-anal plate about as wide as long; plate basal half rectangular, transverse with a longitudinal furrow in middle, setose and slightly bulbous between the furrow; apical half more flattened with margins setose and apical margin truncated (
Fig. 4
C). Subgenital plate triangular, apex truncated. Ovipositor slender and long, longer than posterior femur, slightly curved dorsally; apical dorsal valves slightly shorter than ventral valves (
Fig. 4
D).
Colouration: Head dark red brown; ocelli pale yellow (
Figs. 3
A, 3B, 4A). Frons and genae usually lighter red brown (
Figs. 3
A, 3B), with a light vertical band in females (
Fig. 4
A). Mouthparts medium brown to castaneous; clypeus dark brown with ventral margins and a medial band often castaneous; mandibles yellow brown; palpi pale yellow to yellow brown (
Fig. 3
B). Pronotum dark brown, with a white band along anterior margin that runs from pronotal disc to posterior margin of pronotal lateral lobe (
Fig. 3
A); in females white band not reaching posterior margin of pronotal lateral lobe but form a patch on anterior ventral half of lateral lobe (
Fig. 4
A). Tegmen dark brown; in males, basal third of lateral field white (
Fig. 3
A); in females, veins in lateral field and medial margin white (
Figs. 4
A, 4B). Abdominal tergites blackish brown to red brown; sternites pale yellow. Cerci dark brown. Anterior and middle legs light to medium brown with dark hairs, with some small dark dorsal spots at base of hairs, knees slightly darker; tibiae with ventral surface slightly darker brown. Posterior femur castaneous to red brown and striated, sometimes darker near knees; posterior tibia red brown at base, light brown with dense dark hairs.
Measurement.
See
Table 1
.
Etymology.
The species name refers to highlands in which the cricket is found compared to the
type
species found at lower elevation. From Thai,
khao
= mountain.
Ecology and natural history.
These ground-dwelling crickets can be found at night foraging beneath and among tall grasses (
Fig. 5
) of dry dipterocarp forest in Sakaerat Environmental Research Station (
Fig. 6
). They were observed to feed on the grasses. We did not observe any burrow or male calling during the survey.
FIGURE 5.
Leleja khao
sp. n.
female nymph (A) and adult (B) in its natural habitat, dry dipterocarp forest of Sakaerat.
FIGURE 6.
Dry dipterocarp forest in Sakaerat Environmental Research Station.
TABLE 1.
Measurements (in mm) of
Leleja khao
sp. n.
(mean values in brackets).
BL |
HL |
PL |
PW |
TL |
HFL |
HTL |
OL |
SERS.14.141 |
18.3 |
3.9 |
3.4 |
5.3 |
3.9 |
12.4 |
8.5 |
- |
SERS.14.144 |
18.4 |
3.9 |
3.3 |
5.1 |
3.9 |
12.4 |
8.2 |
- |
Male (n = 2) |
(18.4) |
(3.9) |
(3.4) |
(5.2) |
(3.9) |
(12.4) |
(8.4) |
- |
SERS.14.83 |
23.5 |
3.8 |
4.7 |
6.3 |
3.5 |
15.6 |
10.8 |
16.0 |
SERS.14.145 |
24.2 |
4.0 |
4.3 |
6.0 |
3.6 |
15.1 |
10.0 |
15.8 |
Female (n =2) |
(23.9) |
(3.9) |
(4.5) |
(6.2) |
(3.6) |
(15.4) |
(10.4) |
(15.9) |
Short remark.
In
Tan
et al.
(2015a)
, a typological mistake was found in the description of
Velarifictorus
(
Pseudocoiblemmus
)
bilobus
: Median paramere of epiphallus (= pm) should be correctly labelled as median paramere of ectoparamere.