Iberorhyzobius Raimundo & Canepari gen. nov., for Coccidula rondensis Eizaguirre (Coleoptera: Coccinellidae)
Author
Raimundo, Armando
Author
Canepari, Claudio
Author
Mendel, Zvi
Author
Branco, Manuela
Author
Franco, José Carlos
text
Zootaxa
2006
1312
49
58
journal article
10.5281/zenodo.173892
62fe55c7-9832-42d0-b75d-b5453fd7606b
11755326
173892
Iberorhyzobius rondensis
(
Eizaguirre, 2004
)
,
comb. nov.
Type
material
(not studied by the authors):
SPAIN
:
Holotype
(S1) Puerto de Alijar (
410 m
, altitude), (Sierra de Palmitera, provincia de Málaga, Comunidad de Andalucia,
11.viii.1997
);
Paratypes
(specimens S2S10), collection of Eizaguirre; all the specimens were collected in coniferous (species not mentioned by the author).
Additional material:
PORTUGAL
: Ferraria (Peninsula de Setubal):
5 adults
obtained (
iii–iv.2000
) from larva collected in
20.ii.2000
, on the trunk of
Pinus pinaster
trees infested with
Matsucoccus feytaudi
(1ɗ,
PCAR
; 4Ψ, EFN); Sintra (
Monserrate
):
6 adults
collected in
15.vi.2003
(1ɗ
PCCC
; 1ɗ, 4Ψ EFN);
1 adult
obtained (
iv–v.2004
) from larva, collected idem (
ii–iii.2004
) (1ɗ EFN),
3 adults
obtained (
vi–vii.2004
) from larva idem collected
12.v.04
(1ɗ, 2Ψ EFN).
SPAIN
: Sierra de Gredos: Piedralves, Hi. (
18.v.1934
, coll. C. Koch 2Ψ,
PCCC
,
MSNM
); Vigo: (Before 1927, 1Ψ coll. G. C. Champion,
BMNH
); Malaga: Rd. Ronda – Marbella,
6–20 km
SE Ronda, beating dead cut branches of
Pinus
sp. (
18.v.67
, coll. M. E. Baechus & B. Levey, 1Ψ,
BMNH
).
Distribution
.
Iberorhyzobius rondensis
is only known from the Iberian Peninsula, and is widely distributed from the southeast coast of Andalusia up to the northwestern region of Galicia and
Portugal
(
Fig. 3
). In
Portugal
, the species was found at an altitude range of
25 m
–
600 m
.
Differential diagnosis.
Iberorhyzobius
can be easily differentiated from both
Rhyzobius
and
Coccidula
spp. by several features: absence of prosternal carinae, sparse and fine pubescence, body dimensions and body shape elongated/oval (
Figs. 1–2
).
Specimens of
Coccidula
possess a pair of prosternal carinae joined apically (absent in
Iberorhyzobius
,
Fig. 2
) and body sides almost parallel (
Iberorhyzobius
has an oval shape). Additionally,
Coccidula
exhibits eyes only moderately coarsely faceted (
Iberorhyzobius
differs by the eyes strongly coarsely faceted).
Rhyzobius
differs from
Iberorhyzobius
by the presence of a pair of prosternal carinae (
Figs. 4–5
).
Both
Rhyzobius
and
Coccidula
are distinguished from
Iberorhyzobius
by the dorsal dense pubescence.
Rhyzobius
has ventral and dorsal surfaces of the body covered by yellowish semierect pubescence always distinct (e.g.
Gordon, 1994
). When observed under the binocular microscope the pubescence of
Iberorhyzobius
is fine and sparse. Observation by SEM revealed two distinct kinds of pubescence (
Fig. 2
): i) thinner and abundant and ii) thicker and scattered. The structure of genitalia of
I. rondensis
easily differentiates it from the other
Coccidulini
species (
Fig. 6
) as follows: median lobe elongated, asymmetrical, slightly longer than paramere; sipho elongated and with apex simple; siphonal capsule with outer arm absent. Female genitalia with genital plates very elongated,
infundibulum
and
receptaculum seminis
as in others
Coccidulini
.
FIGURE 1.
Iberorhyzobius rondensis
(Eizaguirre, 2004)
, a—dorsal view; b—antenna.
Description of 4th instar larva.
Body elongate oval, colour brown. Body length
3.6 mm
, body width
1.2 mm
, head width
0.75 mm
, length of front tibiotarsus
0.25 mm
, length of middle tibiotarsus
0.30 mm
. Head distinctly sclerotized, subquadrate; epicranial stem absent; epicranial arms curved laterally from vertex to three fourths of the head then directed laterally for the last fourth; antennae threesegmented. Prothorax subtrapezoidal with lateral margin crenulate and with a lateral series of chalazae. Meso and metathorax with series of lateral and dorsolateral chalazae. Abdomen 9segmented with series of lateral and dorsolateral strumi covered in each margin by 5–6 chalazae.
Natural history.
Larvae were collected on belt traps installed on tree trunks to study the phenology of the maritime pine bast scale, in central and southern
Portugal
, and were observed to feed on the eggs of this scale insect (
Fig. 5
). Larvae showed a kairomonal response to the sex pheromone of the prey,
M. feytaudi
(
Branco
et al.
2006
)
. Adults are also attracted to the prey sex pheromone, but they display a weaker response. Observations taken from
2000 to 2006
, using both tree belt traps and tree arenas, set up with rubber dispensers loaded with the sex pheromone of the prey, showed that larvae were only active from February to MayJune. Adults were observed only in MayJune. These data suggest a univoltine life cycle.