Scorpions of Ethiopia (Arachnida: Scorpiones). Part II. Genus Babycurus Karsch, 1886 (Buthidae), with description of two new species
Author
Kovařík, František
Author
Lowe, Graeme
Author
Seiter, Michael
Author
Plíšková, Jana
Author
Šťáhlavský, František
text
Euscorpius
2015
196
1
31
journal article
1536-9307
EE3FF040-565B-42F5-8D60-C83D7AAD01E7
Babycurus sofomarensis
Kovařík, Lowe, Seiter, Plíšková et Šťáhlavský
,
sp. n.
(
Figures 46–55
,
58–61
,
64–65, 67–77
,
87–102
,
123
,
Table 2
)
http://zoobank.org/urn:lsid:zoobank.org:act:D7544F
0F-65FB-48F5-AFB6-07BBB6373503
TYPE LOCALITY AND
HOLOTYPE
DEPOSITORY
.
Ethiopia
,
Oromia State
,
Arsi Province
,
Sof Omar
,
06°54'19"N
40°51'04"E
,
1200 m
a.s.l.
;
FKCP
.
Figures 18–23:
Babycurus dunlopi
sp. n.
Figures 18
,
20–22.
Holotype female, chelicerae, carapace and tergites I–III (18), distal segments of legs III (20) and IV (21), retrolateral view, sternopectinal region and sternites III–IV (22).
Figures 19, 23:
Paratype male, chelicerae, carapace and tergites I–III (19), and sternopectinal region and sternite III (23).
B. wituensis
..
|
B. dunlopi
sp. n.
|
DIMENSIONS
(
MM
)
|
♀
lectotype
|
♀
holotype
|
♂
paratype
|
Carapace L / W |
4.7 / 4.7 |
5.9 / 6.3 |
5.75 / 5.8 |
Mesosoma L |
16.7 |
17.7 |
13.3 |
Tergite VII L / W |
3.43 / 5.11 |
4.1 / 6.2 |
3.8 / 5.15 |
Metasoma and telson L |
23.7 |
29.55 |
30.2 |
Segment I L / W / H |
2.7 / 2.7 / 2.28 |
3.35 / 3.40 / 3.0 |
3.5 / 3.2 / 2.85 |
Segment II L / W / H |
3.2 / 2.8 / 2.32 |
4.1 / 3.5 / 3.05 |
4.1 / 3.4 / 2.8 |
Segment III L / W / H |
3.5 / 2.8 / 2.34 |
4.5 / 3.65 / 3.4 |
4.65 / 3.65 / 2.9 |
Segment IV L / W / H |
4.1 / 1.5 / 2.47 |
5.3 / 3.7 / 3.4 |
5.4 / 3.75 / 3.2 |
Segment V L / W / H |
4.9 / 2.5 / 2.21 |
6.3 / 3.7 / 3.4 |
6.45 / 4.15 / 3.05 |
Telson L / W / H |
4.7 / 1.61 / 1.59 |
6.0 / 2.65 / 2.35 |
6.1 / 2.45 / 2.15 |
Pedipalp L |
16.5 |
21.8 |
21.35 |
Femur L / W |
3.9 /1.3 |
5.2 / 1.8 |
5.15/ 1.6 |
Patella L / W |
4.6 / 1.7 |
6.2 / 2.5 |
6.1 / 2.45 |
Chela L |
8 |
10.4 |
10.1 |
Manus L / W / H |
2.6 / 1.7 / 1.78 |
3.8 / 2.45 / 2.45 |
4.15 / 2.9 / 2.75 |
Movable finger L |
5.4 |
6.6 |
5.95 |
Total L |
45.1 |
53.15 |
49.25 |
Table 1:
Comparative measurements of adults of
Babycurus wituensis
Kraepelin, 1913
and
B. dunlopi
sp. n.
Abbreviations: length (L),
posterior width), depth (H).
Figures 24–37: Figures 24–28:
Babycurus wituensis
Kraepelin, 1913
.
Figures 24–26.
Lectotype female, pedipalp chela dorsal view (24), pedipalp movable finger, dorsal view (25) and telson, lateral view (26).
Figures 27–28.
Telson, lateral views female (27) and male (28) from Kenya, Mombasa area, 04°13'32.99"N 39°35'13.56"E, leg. Alex Ullrich, FKCP.
Figures 29–37:
Babycurus dunlopi
sp. n.
Figures 29–31, 36
, holotype female, pedipalp chela, dorsal (29), external (30), pedipalp movable finger, dorsal view (31) and telson, lateral view (36).
Figures 32–34, 37
, paratype male, pedipalp movable finger, dorsal view (32), pedipalp chela, dorsal (33), external (34), and telson, lateral view (37).
Figures 35
, paratype male, telson, lateral view.
Figures 38–40:
Lectotype female of
Babycurus wituensis
Kraepelin, 1913
, Pokomonie, Tanganyika, now Tanzania, ZMHB, dorsal (38) and ventral (39) views and chelicerae, carapace and tergites I–III (40). The original labels are also included in the plate.
TYPE MATERIAL
.
Ethiopia
,
Oromia State
,
Arsi Province
,
Sof Omar
,
06°54'19"N
40°51'04"E
,
1200 m
a.s.l.
(
Fig. 95
, locality
No.
13
EC
),
24-25.
VI
.2013
,
4♂
(
paratypes
) (
UV
detection), leg.
F. Kovařík
,
J. Plíšková
&
P. Novák
,
23-24.XI.2014
,
2♂
(
paratypes
)
1♀
(
holotype
) (
UV
de- tection), leg.
F. Kovařík
;
Oromia State
,
West Harerge
,
07°44'37"N
40°42'39.5"E
,
1234 m
a.s.l.
(
Fig. 96
, locality
No.
14
EO
),
24-25.XI.2014
,
1♂
(
paratype
) (
UV
detection),
Oromia State
,
West Harerge
,
07°46'39.7"N
40°37'12.4"E
,
800 m
a.s.l.
(
Fig. 97
, locality
No.
14
EP
),
25.XI.2014
,
1juv.
(
paratype
). All type specimens are in 80 % alcohol in the first author’s collection (
FKCP
), except for a juvenile
paratype
which is alive (
Fig. 98
).
ETYMOLOGY. Named after the
type
locality.
DIAGNOSIS. Total length
32–35 mm
(males) and
46 mm
(female). Coloration yellowish brown to grey with darker markings. Chelicerae yellow without reticulation. Pedipalp movable fingers with 6 principal rows of denticles and an apical row of four denticles. Pectines with 18–20 teeth in both sexes. First metasomal segment has 10 carinae, second through fourth segments have eight carinae. Telson setose, smooth, with a short and pointed subaculear tooth. Vesicle elongate, ellipsoidal. Aculeus curved, shorter than vesicle. Sexual dimorphism minor, adult males with fingers of pedipalps more flexed proximally and slightly shorter fingers; there is no difference in length and width of chela of pedipalps (ratio chela length to manus width
3.5–3.8 in
both sexes) or metasomal segments (ratio metasomal segment V length to width 2.8–3.0 in both sexes); posterior margin of sternite V without smooth median patch in both sexes.
Figures 41–43:
Babycurus dunlopi
sp. n.
, paratype male (41), holotype female before maturity ecdysis (42), holotype female shortly after maturity ecdysis 4.V.2014 (43).
Figures 44–45:
Babycurus dunlopi
sp. n.
, the type locality (Ethiopia, Oromia State, Gemu Gofa region, Arba Minch, 05°59'25.4"N 37°32'24"E, 1261 m a.s.l.).
Figures 46–49:
Babycurus sofomarensis
sp. n.
Figures 46–47.
Paratype male from the type locality, dorsal (46) and ventral (47) views.
Figures 48–49.
Holotype female, dorsal (48) and ventral (49) views.
Figures 50–55:
Babycurus sofomarensis
sp. n.
Figures 50–52.
Paratype male from the type locality, metasoma and telson, lateral (50), ventral (51), and dorsal (52) views.
Figures 53–55.
Holotype female, metasoma and telson, lateral (53), ventral (54), and dorsal (55) views.
DESCRIPTION. Total length
32–35 mm
(males) and
46 mm
(female). Measurements of the carapace, telson, segments of the metasoma and segments of the pedipalps are given in
Table 2
. Coloration (
Figs. 46–49
,
62– 63
) base yellowish brown to grey with darker markings on patella and femur of legs and pedipalps, carapace, and. Tergites I-VI almost grey. Tergite VII, tibia of legs, manus of pedipalps and metasomal segments I–III usually lighter. Chelicerae yellow without reticulation. (
Fig. 63
).
Sexual dimorphism
minor, adult males with fingers of pedipalps more flexed proximally (
Figs. 88 and 90– 91
) and shorter fingers (ratio chela length to movable finger length
1.56 in
female and
1.70–1.75 in
males); there is no difference in length and width of chela of pedipalps (ratio chela length to manus width
3.5– 3.8 in
both sexes) or metasomal segments (ratio metasomal segment V length to width 2.8–3.0 in both sexes).
Figures 56–61: Figures 56–57.
Babycurus subpunctatus
, female from locality 14EI, distal segments of legs III (56) and IV (57), retrolateral view.
Figures 58–61.
Babycurus sofomarensis
sp. n.
, holotype female, distal segments of legs I (58), II (59), III (60) and IV (61), retrolateral view.
CHELICERAE (
Figs. 64
). With dentition typical for the genus, teeth sharp. Tegument basally smooth and shiny without granulation.
PEDIPALPS (
Figs. 69–75
). Femur granulated, with five granulate carinae developed. Patella almost smooth with seven granulate carinae developed. Chela with sparsely granulated carinae present, smooth; fingers long (ratio chela length movable finger length 1.56–1.75), curved, with 6 principal rows of denticles, 5 of them terminating in two external granules; the last row has one external granule in the middle of the row. There are also five or six internal granules. Movable fingers bear apical row of four denticles and three terminal accessory denticles.
CARAPACE (
Figs. 64–65
). Slightly trapezoidal (narrower anteriorly) and slightly longer than wide, or as long as wide; anterior margin slightly convex, with some short microsetae. Carination absent. Median and posterior lateral furrows wide and deep, other vestigial to absent. Tegument densely and coarsely granulose. Median eyes large and raised; five pairs of lateral eyes: three samesized and aligned along each anterolateral corner, plus two vestigial to absent.
B. subpunctatus
.
|
B.
|
. |
Dimensions
|
♀
Holotype
|
♀
14EI
|
♂
14EI
|
♀
Holotype
|
Carapace |
L / W |
3.4 / 3.2 |
3.6 / 3.3 |
2.85 / 2.6 |
5.1 / 4.9 |
Mesosoma |
L |
10.3 |
9.9 |
6.4 |
15.2 |
Tergite VII |
L / W |
2.17 / 3.33 |
2.45 / 3.75 |
1.75 / 2.7 |
3.7 / 4.7 |
Metasoma et telson |
L |
18.4 |
18.75 |
13.2 |
25.7 |
Segment I |
L / W / H |
2.2 / 1.8 / 1.43 |
2.3 / 2.0 / 1.7 |
1.55 / 1.4 / 1.25 |
3.1 / 2.7 / 2.45 |
Segment II |
L / W / H |
2.6 / 1.6 / 1.37 |
2.4 / 1.8 / 1.6 |
1.95 / 1.3 / 1.25 |
3.65 / 2.5 / 2.4 |
Segment III |
L / W / H |
2.9 / 1.6 / 1.36 |
3.05 / 1.75 / 1.6 |
2.05 / 1.25 / 1.2 |
4.1 / 2.55 / 2.4 |
Segment IV |
L / W / H |
3.2 / 1.5 / 1.36 |
3.45 / 1.75 / 1.6 |
2.45 / 1.25 / 1.2 |
4.6 /2.45 / 2.4 |
Segment V |
L / W / H |
4.0 / 1.5 / 1.38 |
4.15 / 1.7 / 1.6 |
2.85 / 1.15 / 1.1 |
5.6 / 2.35 / 2.2 |
Telson |
L / W / H |
3.2 / 1.10 / 1.17 |
3.4 / 1.25 / 1.2 |
2.35 / 0.8 / 0.93 |
4.65 / 1.55 / 1.7 |
Pedipalp |
L |
13 |
13.5 |
9.75 |
17.05 |
Femur |
L / W |
3.0 / 1.0 |
3.35 / 1.075 |
2.35 / 0.8 |
4.2 / 1.35 |
Patella |
L / W |
3.9 / 1.3 |
4.0 / 1.35 |
2.8 / 1.05 |
5.05 / 1.75 |
Chela |
L |
6.1 |
6.15 |
4.6 |
7.8 |
Manus |
L / W / H |
2.2 / 1.3 / 1.3 |
2.7 / 1.4 / 1.3 |
1.65 / 0.9 / 0.83 |
2.8 / 2.05 / 1.95 |
sofomarensis
sp. n.
♂
|
♂
14EN
14EO
|
3.9 / 3.5 |
3.9 / 3.8 |
10.6 |
9.0 |
2.9 / 3.4 |
2.6 / 3.4 |
20.2 |
19.57 |
2.45 / 2.25 / 2.0 |
2.3 / 2.15 / 1.9 |
2.9 / 2.2 / 1.9 |
2.8 / 2.05 / 1.8 |
3.2 / 2.15 / 1.9 |
3.1 / 2.05 / 1.8 |
3.6 / 2.15 / 1.9 |
3.6 / 2.0 / 1.8 |
4.65 / 2.1 / 1.8 |
4.52 / 1.9 / 1.75 |
3.4 / 1.2 / 1.3 |
3.25 / 1.1 / 1.25 |
14 |
13.45 |
3.3 / 1.1 |
3.2 / 1.05 |
4.05 / 1.45 |
3.9 / 1.45 |
6.65 |
6.4 |
2.8 / 1.9 / 1.75 |
2.7 / 1.67 / 1.67 |
3.85 |
3.7 |
34.7
|
32.37
|
Movable finger |
L |
3.9 |
3.45 |
2.95 |
5.0 |
Total |
L |
32.1 |
32.25 |
22.45 |
46 |
Table 2:
Comparative measurements of adults of
Babycurus subpunctatus
Borelli, 1925
and
B. sofomarensis
sp. n.
Abbreviations:
corresponds to posterior width), depth (H). MESOSOMA (
Figs. 46–49
,
64–65
). Tergites I–VI bear one conspicuous median carina; tergite VII with five welldefined carinae (median, submedians and laterals), which are long and serrate to crenulate. All tergites are densely and coarsely granulose mainly on posterior part. Sternum (
Figs. 67–68
) standard for the genus:
type
1, triangular in shape; medial depression large. Pectines standard-sized for the genus (
Figs. 67–68
): extending to around a quorter of sternite IV in both sexes, setose. Tooth count 18–20 (1x18, 7x19, 5x20) in males and 18/
18 in
female. Pectines have 3 marginal lamellae and 7 middle lamellae. Sternites lack carinae, surfaces are smooth and sparsely setose. Posterior margin of sternite V without smooth median patch in both sexes.
Figures 62–68: Figures 62–63
,
66.
Babycurus subpunctatus
from locality 14EI, chelicerae, carapace and tergites I–III of male (62) and female (63), and sternopectinal region and sternites III–IV of male (66).
Figures 64–65
,
67–68.
Babycurus sofomarensis
sp. n.
, chelicerae, carapace and tergites I–III of paratype male from the type locality (64) and holotype female (65), and sternopectinal region and sternite III of male paratype from the type locality (67) and holotype female (68).
Figures 69–79: Figures 69–76.
Babycurus sofomarensis
sp. n.
, holotype female, pedipalp chela, dorsal (69), external (70), and ventral (71) views. Pedipalp patella, dorsal (72) and external (73) views. Pedipalp femur, internal (74) and trochanter and femur dorsal (75) views. The trichobothrial pattern is indicated in Figures 70–75. Telson, lateral view (76).
Figure 77.
Babycurus sofomarensis
sp. n.
, paratype male from the type locality, telson, lateral view.
Figures 78–79.
Babycurus subpunctatus
from locality 14EI, telson, lateral views of female (78) and male (79).
Figures 80–92: Figures 80–86:
Babycurus subpunctatus
.
Figures 80–82.
Holotype female, pedipalp chela dorsal (80), and external (81) views, and pedipalp movable finger, dorsal view (82).
Figures 83–84.
Female from locality 14EI, pedipalp chela dorsal (83), and external (84) views.
Figures 85–86.
Male from locality 14EI, pedipalp chela dorsal (85), and external (86) views.
Figures 87–92:
Babycurus sofomarensis
sp. n.
Figures 87–88.
Holotype female, pedipalp chela dorsal (87), and external (88) views.
Figures 89–90.
Paratype male from the type locality, pedipalp chela dorsal (89), and external (90) views,
Figures 91–92.
Paratype male from locality 14EO, pedipalp chela external view (91), and pedipalp movable finger, dorsal view (92).
Figures 93–94:
Babycurus sofomarensis
sp. n.
, male paratype (93) and female holotype at the type locality.
Figures 95–96:
Localities of
Babycurus sofomarensis
sp. n.
.
Figure 95.
The type locality (Ethiopia, Oromia State, Arsi Province, Sof Omar, 06°54'19"N 40°51'04"E, 1200 m a.s.l.).
Figure 96.
Locality 14EO (Ethiopia, Oromia State, West Harerge, 07°44'37"N 40°42'39.5"E, 1234 m a.s.l.).
Figures 97–98:
Locality of
Babycurus sofomarensis
sp. n.
14EP (Ethiopia, Oromia State, Harerge, 07°46'39.7"N 40°37'12.4"E, 800 m a.s.l.) and paratype juvenile (98) at the locality down at the valley from Figure 97.
Figures 99–101:
Left hemispermatophore of paratype male of
Babycurus sofomarensis
sp. n.
from the type locality.
Figure 99.
Concave aspect.
Figure 100.
Convex aspect.
Figure 101.
Convex aspect. Enlarged view of lobes at base of flagellum.
Figure 102:
Chromosomes of paratype males of
Babycurus sofomarensis
sp. n.
from the type locality (2n = 22).
A
) Male mitotic metaphase.
B
) Karyogram based on previous metaphase.
C
) Postpachytene, cell with decavalent - arrows indicate chromosomes of multivalent. The first and second largest chromosomes of karyotype marked as 1 and 2.
D
) Idiograms of the first (grey) and the second (white) analyzed males. Bar = 5 μm.
LEGS (
Figs. 56–61
). The tarsomeres bear two rows of macrosetae on the ventral surface and numerous macrosetae on the other surfaces; bristle combs absent. Femur bears only solitary macrosetae. Femur coarsely granulose, femur and patella with carinae developed. Tibial spurs present on fourth legs.
METASOMA AND TELSON (
Figs. 50–55
). All segments with granulate complete carinae developed except for carinae on segment V in males which are vestigial. The carinae are composed of minute, rounded, equal-sized, and evenly spaced granules. The first metasomal segment has a total of 10 carinae, the second through fourth segments have eight carinae, and the fifth segment has five carinae. All metasomal segments are sparsely granulated. Metasoma is very sparsely hirsute. Telson smooth with only a weakly indicated ventral carina and a dense cover of long hairs near the subaculear tooth. (
Figs. 76–77
). Subaculear tooth short and pointed. Vesicle elongate, ellipsoidal. Aculeus curved, shorter than vesicle.
HEMISPERMATOPHORE (
Figs. 99–101
). Trunk elongate, slender; flagellum short, filiform, pars recta 0.25 times length of trunk; pars reflecta 0.8–1.0 times length of pars recta (measured from left and right hemispermatophores of
paratype
male), much smaller in diameter; structure of lobes at base of flagellum similar to that described for
B. exquisitus
(
Lowe, 2000
)
, including two elongate, laminate lobes (inner and outer), lacking a third median lobe; inner lobe broad with longitudinal median carina, apex rounded; outer lobe narrow with longitudinal median carina, apex tapered; basal lobe weak, forming obliquely transverse carinae reaching outer basal edge of inner lobe; carina of inner lobe joined with basal lobe carina; measurements: trunk L (to base of flagellum)
3.73 mm
, pars recta L
0.98 mm
, inner lobe L (from base of flagellum)
0.30 mm
, outer lobe L
0.26 mm
.
Figures 103–109:
Holotype female of
Babycurus subpunctatus
Borelli, 1925
, Somalia, Cuban Cubu; MCSN, dorsal (103) and ventral (104) views, sternopectinal region and sternite III (105), telson lateral view (106), and metasoma and telson, lateral (107), ventral (108), and dorsal (109) views. The original label is also included in the plate.
Figures 110–113:
Babycurus subpunctatus
Borelli, 1925
from locality 14EI.
Figures 110–111.
Male, dorsal (110) and ventral (111) views.
Figures 112–113.
Female, dorsal (112) and ventral (113) views.
Figures 114–119:
Babycurus subpunctatus
Borelli, 1925
from locality 14EI.
Figures 114–116.
Male, metasoma and telson, lateral (114), ventral (115), and dorsal (116) views.
Figures 117–119.
Female, metasoma and telson, lateral (117), ventral (118), and dorsal (119) views.
CYTOGENETIC DATA (
Fig. 102
). We analyzed
two paratype males
using standard cytogenetic methods (e.g.
Kovařík et al., 2009
;
Šťáhlavský et al., 2014
). The dip- loid complement of analyzed material is composed of 22 holocentric chromosomes (
Fig. 102A
). The first two chromosomes show considerable difference in size within both analyzed males (
Fig. 102D
). The first chromosome forms 10.75% (SD=0.63) of the diploid set in
one male
(the number of measured mitotic metaphases is 13) and 10.84% (SD=0.17) in the second male (the number of measured mitotic metaphases is 9). The second chromosome forms 7.84% (SD=0.41) in
one male
and 8.46% (SD=0.90) in the other. The rest of chromosomes decrease gradually in size from 6.28% to 2.48% or from 5.99% to 2.33%, respectively (
Fig. 102B, D
). The conspicuous difference of the size of the first two chromosomes may be explained by reciprocal translocations between different chromosome pairs. This type of chromosomal rearrangement forms multivalents during meiosis and may cause chromosomal different- iation of size (e.g. Kovařík et al., 2013). We observed only limited number of postpachytene. However in all cases we found multivalents formed by ten chromosomes (in one cell of the first male and in four cells in the second male) (
Fig. 102C
). Moreover, in one cell we found decavalent and tetravalent together. It is evident that two chromosomes from this decavalent are the largest elements of the set and correspond to the first and second chromosomes of the karyotype (
Fig. 102C
, chromosomes marked 1 and 2)
AFFINITIES. The described features distinguish
B. sofomarensis
sp. n.
from all other species of the genus.
B. sofomarensis
sp. n.
seems to be closest to
B. subpunctatus
from which can be unequivocally separated by:
1)
total length
32–35 mm
(males) and
46 mm
(female) in
B. sofomarensis
sp. n.
and
22.5 mm
(male) –
32.25 mm
(females) in
B. subpunctatus
;
2)
coloration darker in
B. sofomarensis
sp. n
(
Figs. 64–65
versus 62– 63);
3)
pectines with 18–20 teeth in
B. sofomarensis
sp. n.
and 16–17 teeth in
B. subpunctatus
;
4)
chela broader in
B. sofomarensis
sp. n
(ratio chela length to manus width
3.5– 3.8 in
both sexes) than in
B. subpunctatus
(ratio chela length to manus width
5.1 in
male and
4.3– 4.6 in
females);
5)
male of
B. sofomarensis
sp. n.
with fingers of pedipalps flexed proximally (
Figs. 88 and 90– 91
) and almost straight in both sexes of
B. subpunctatus
(
Figs. 81, 84
, and 86).
Figures 120–122:
Babycurus subpunctatus
Borelli, 1925
, locality 14EI (120), Ethiopia, Somali State, Liben region, between Filtu and Dolo Odo, 04°50'07.5"N 40°55'13.5"E, 912 m a.s.l., male (121) and female (122) at the locality.
Figure 123:
Map showing the known distribution of
Babycurus
in Ethiopia.
COMMENTS ON LOCALITIES AND LIFE STRATEGY. We visited the type locality for the first time on
24 June 2013
. We spent a night there and collected several types of
Pandinus trailini
Kovařík, 2013
(see Kovařík, 2013: 10, figs. 34–35). At the locality in the valley formed by the Gestro River on
24–25 June 2013
we recorded nighttime temperatures of 19.4 ºC shortly after sunset, dropping to 15.6 ºC (minimum temperature) before sunrise and up to 69% humidity. We collected at night with UV light
four male
paratypes
. We visited the type locality again on
23 November 2014
and at night the first author (FK) recorded nighttime temperatures of 23.3 ºC shortly after sunset, dropping to 19 ºC (minimum temperature) before sunrise and up to 64% humidity. The first author (FK) collected at night with UV light two other male
paratypes
and the female
holotype
. In addition to
B. sofomarensis
sp. n.
, he recorded at this locality
P. trailini
,
Hottentotta trilineatus
(Peters, 1861)
, and
Iomachus
sp.
Next night we spent at the locality 14EO (
Fig. 96
). Here, the first author (FK) recorded on
24–25 November 2014
, shortly after sunset, a nighttime temperature of 22.7 ºC, which gradually dropped to 16 ºC (minimum temperature) before sunrise. Humidity during the night varied between 70% and 65%. Several specimens of
Hottentotta trilineatus
and a
paratype
of
B. sofomarensis
sp. n.
were found around 22:00 h (temperature 19 ºC).
The last
paratype
juvenile (
Fig. 98
) was collected during the day under a big stone at the locality 14EP (
Fig. 97
) in the valley formed by the Wabe Shebelle River. Apart from
B. sofomarensis
sp. n.
we recorded
Pandinus platycheles
Werner, 1916
and
Hottentotta trilineatus
at this locality.