First Record of Dericorys albidula Serville, 1838 (Orthoptera: Dericorythidae) in Tunisia and Libya
Author
Tlili, Haithem
Author
Abdellaoui, Khemais
Author
Chouikha, Manel Ben
Author
Mhafdhi, Mouna
Author
Jemmazi, Adel
Author
Ammar, Mohamed
Author
Desutter-Grandcolas, Laure
text
Zootaxa
2019
2019-02-01
4551
3
385
393
journal article
27594
10.11646/zootaxa.4551.3.7
0fe8dc15-68ce-4ff6-a62a-897ea2349506
1175-5326
2623000
50EFEDBF-4F07-4E73-9537-3E76F52050AF
Dericorys albidula
Serville, 1838
Dericorys albidula
Serville, 1838
: 639
.
Dericoris acutispina
Stål, 1875
: 27
.
Derocorystes curvipes
(
Redtenbacher, 1889
)
: 29.
Cyphophorus tibialis
(Fieber, 1853)
: 121.
FIGURE 2
. Habitus of
Dericorys albidula
Serville, 1838
: A–C, Lectotype female, dorsal view (A), lateral view (B), labels (C); D–E, Female from Tozeur, Tunisia, lateral view (D), dorsal view (E); F–G. Male from Tozeur, Tunisia, lateral view (F), dorsal view (G). Scale bar 1 cm.
Type
locality:
Serville (1838)
indicated that
D. albidula
originates from “
Egypt
. Mont-Liban”, separating the two origins.
One
of the labels of the female
type
(
Fig. 2
A-C) indicates “désert du
Sinaï
” [desert of
Sinaï
], which is located in
Egypt
; the other label of the female
type
“1806 / 33” (“entry
1806 in
the year 1833” in the catalogue of
MNHN
collections) confirms this origin (year 1833, specimen 1806, origin
Egypt
,
Sinaï
, collector
D. Bové
)
.
The male
type
may then have originated from Mount
Lebanon
, located at that time in the
Ottoman Empire
and now located in
Lebanon
and
Syria
. As the male
type
may be lost (cf infra), the
type
locality of
D. albidula
must be restricted to
Egypt
, Desert of the
Sinaï
.
Type material.
LECTOTYPE
(here designated):
1 female
labelled as follows: 1806 33 (small, rounded green label, handwritten) /MUSÉUM PARIS, désert du
Sinaï
, Bové 1833 (white, rectangular label, handwritten) /
D. albidula
Serv., M. Bové
(white, rectangular label bordered with black, handwritten)/
Dericorys albidula
Serville
(handwritten by Serville) / TYPE (white label, printed in red) /
LECTOTYPE
(red label, printed in black) /
Lectotype
désigné par L. Desutter-G randcolas. et Tlili H.
viii 2018
(white label, handwritten) / MNHN-EO- CAELIF163 (white label, printed in black). Examined.
Remark.
Serville (1838)
listed one female and one male types, but the male seems to have been lost very early, as only the female is mentioned in early papers on the species (
Pictet & Saussure 1887
; Bolívar 1913; Chopard 1943). The female type is thus here designated as
lectotype
, to fix the taxonomy of the species. Photos of the female type can be seen on the MNHN collection database at the following address https://science.mnhn.fr/taxon/ species/dericorys/albidula;
Habitus and labels are also shown in figure (
Fig. 2
).
Other materials examined.
TUNISIA
:
Tozeur
,
Degueche
,
33°57'51.4''N
,
8°11'12.6''E
,
46 m
, 26.
vi.2017, 3
♂
4 ♀
,
H. Tlili
(
INAT
)
;
Tozeur
,
Gouifla
,
34°08'46.7''N
,
8°17'38.9''E
,
53 m
,
02.vi.2016
,
H. Tlili
,
1 ♂
(MNHN-EO- CAELIF 4715),
1 ♀
(MNHN-EO-CAELIF 4716),
1 ♂
(
INAT
)
.
ALGERIA
:
Touggourt
,
vi.1928, 1
♀ (MNHN-EO-CAELIF 2511)
.
FIGURE 3.
Dericorys albidula
Serville, 1838
, male genitalia. A, dorsal view (membrane and epiphallus removed); B, lateral view; C, endophallus, lateral view; D, epiphallus; E, entire male phallic complex. Line drawings modified after Dirsh, 1975. Abbreviations: Ac, arch of cingulum; Ap, apical valves of penis; Apd, Apodemes; Bp, Basal valves of penis; Cv, valves of cingulum; Edj, ejacualtory duct.; Ejs, ejacualtory sac; Gpr, gonopore processes; Rm, rami of cingulum; Sps, spermatophore sac.
IRAN
:
Kerman
, 12.
vii.1964, 3
♀ (MNHN-EO-CAELIF 5002, MNHN-EO-CAELIF 5004, MNHN-EO- CAELIF 5005)
.
CHAD
:
Eguei
,
Tourka
27.
vii.1935, 3
♂ (MNHN-EO-CAELIF 164, MNHN-EO-CAELIF 5003, MNHN-EO- CAELIF 5006)
1 ♀
(MNHN-EO-CAELIF 165, MNHN-EO-CAELIF 5000 MNHN-EO-CAELIF 5001);
Borkou
, Faya 20.
viii.1935, 1
♀ (MNHN-EO-CAELIF 5007)
.
FIGURE 4
. Typical habitat of halophytic
Anabasis articulata
in desert steppes (Tozeur, Gouifla 2017) with a preference for salinized soils (Aronson 1989). (Photo H. Tlili).
LIBYA
: Tiji,
11°21'16.0"N
32°00'52.9"E
, 7.
vi.1957,
1
♀, K.M. Guichard, identified
D. albidula
by E. Morales in 1959, NHM (box address:
Orthoptera
9
Caelifera
2 Acrididea N° 58).
Diagnosis:
After Dirsh (1965). Large and robust, integument finely rugose. Antenna thick, filiform; yellowwhitish, with 20 segments, slightly shorter than head and pronotum together. Pronotum with a strong crest. Wings yellowish-green with a smoky spot at the tip. Hind tibia curved; reddish at the apex on inner face; arolia more than half the length of the claws (
Fig. 2
). Male phallic complex as in
Fig. 3
.
Distribution:
D. albidula
is well-known in Central Asia, more specifically in the province of
Qom
in
Iran
(Jabbari
et al.
2015) and in
Uzbekistan
(Gapparov
et al
. 2016), where it causes huge devastation in the Saxaul tree (
Haloxylona phyllum
and
H
.
persicum
) (
Tokgayev 1973
; Gapparov
et al
. 2016).
D. albidula
was also recorded in central Arabia where mass multiplication occurred some years ago (
Popov 1980
). The presence of
D. albidula
in northern Africa was attested by Chopard (1943), who listed specimens from
Chad
and from
Algeria
, while the species is attested in
Egypt
by the
type
locality and in the Wadi Gennesh and the Wadi Amara (
Walker 1870
).
D. albidula
is here newly recorded from
Libya
and
Tunisia
(Fig. 6).
Measurements (mm):
Males
(n = 10) Body length 52–59 (mean = 55,8); pronotum length 8–10,3 (mean = 9,2); pronotum height 8–10,6 (mean = 9,53); tegmen length 41,7–46 (mean = 44,2); hind femur length 22–24,5 (mean = 23,2); hind femur height 5,5–5,9 (mean = 5,7).
Females
(n = 14) Body length 65–72 (mean = 67,9); pronotum length 11,7–13 (mean = 11,9); pronotum height 11–13,4 (mean = 12,2); tegmen length 51–56,3 (mean = 53,4); hind femur length 25,7–31 (mean = 28); hind femur height 5,7–6.6 (mean = 6,2).
Habitat and biology:
According to our observations,
D. albidula
has a preference for sandy areas where
Anabasis articulata
grows, as shown in figure 4. This grasshopper has an univoltine life cycle, overwintering exclusively in the egg stage. Hatchings typically pass through five nymphal instars before the final moult into the adult stage. Adult females deposit their eggs in the soil in egg-pods in July. Nymphal development begins in late March and ends in late May when host plants are usually green and fresh. It takes approximately one month and a half for nymphs to become adults, and two additional weeks to attain sexual maturity. Adults survive into late September or early October according to weather conditions. All stages of development, nymph, imaginal moult and adult mating occur on the halophytic
A. articulata
(
Fig. 5
).
We surveyed grasshopper species assemblages in several Tunisian localities harbouring the habitat described as specific for
D. albidula
. We found
D. albidula
in only two localities among the 12 sampled (
Table 1
). Neither the presence of
A. articulata
, nor the presence of sandy soil are sufficient to explain the presence vs the absence of the species.
FIGURE 5
. Habitus and coloration of
Dericorys albidula
as nymphs and adults.
A
, 3
rd
nymphal instar;
B
, final moult into the adult stage;
C
, adult male;
D
, adult female. Photos C and D show the differences in tegument coloration between young adult (C) and old adult (D). (Photos H. Tlili).
TABLE 1.
Localities where grasshoppers were collected in Southern Tunisia: presence / absence of
D. albidula
Serville, 1838
in comparison with some main ecological variables of the sites.
Province |
Localities |
D. albidula
|
A. articulata
|
Sandy areas |
Sheep trails |
Kasserine |
F'his |
- |
- |
- |
- |
Mehreza |
- |
- |
- |
- |
Sbeitla |
- |
- |
- |
- |
Gafsa |
Douwara |
- |
+ |
+ |
- |
El Guetar |
- |
+ |
- |
- |
Sened |
- |
+ |
- |
- |
Kebili |
Essagui |
- |
+ |
- |
+ |
Chott el faranig |
- |
+ |
+ |
- |
Rahmet |
- |
- |
- |
- |
Tozeur |
Degache |
+ |
+ |
+ |
+ |
Souani Ali |
- |
- |
- |
- |
Gouifla |
+ |
+ |
+ |
+ |
In the two populations sampled, 5 to
7 juveniles
of
D. albidula
were typically found on each
A. articulata
plant, while later in the season most
A. articulata
plants were occupied by only one adult, except when one male and one female were engaged in mating.
All data will be published in forthcoming papers describing the grasshopper assemblages in
Tunisia
, and the biology of the species (Tlili, pers. obs.).