Pygmy chameleons of the Rhampholeon platyceps compex (Squamata: Chamaeleonidae): Description of four new species from isolated ‘ sky islands’ of northern Mozambique
Author
Branch, William R.
Author
Bayliss, Julian
Author
Tolley, Krystal A.
text
Zootaxa
2014
3814
1
1
36
journal article
36839
10.11646/zootaxa.3814.1.1
493d9746-7061-41d2-8bff-0713bd07f56f
1175-5326
286211
A024EBCC-AD60-4104-AD4A-4E4843CE6983
Rhampholeon
(
Rhinodigitum
)
bruessoworum
sp. nov.
Mount Inago Pygmy Chameleon
Synonymy:
Rhampholeon
sp. Bayliss
et al
. 2010, p17. fig. 13.
Etymology
. The specific epithet honours the contributions of the brothers Carl and Darren Bruessow to the protection of wildlife in southern
Malawi
, particularly via the Mount Mulanje Conservation Trust.
Types
.
The
type
series comprises three specimens, including:
Holotype
.- An adult female (
PEM
R20375;
Fig. 9
A) collected by J. Bayliss,
5 September 2009
, in a small patch of wet forest at the base of a granite inselberg of Mt. Inago, Zambézia Province,
Mozambique
(15˚04'51”S 37˚23'37”E, ca
1478 m
a.s.l.).
FIGURE 9.
Rhampholeon bruessoworum
sp. nov.
: A—Holotype; B—Allotype; C—Habitat on Mt. Inago (J. Bayliss).
Allotype
. An adult male (
PEM
R20376,
Fig. 9
B), same collecting details as
holotype
.
Paratype
. An adult female (
PEM
R20374), same collecting details as
holotype
.
Meristics.
Measurements of the
type
series of
Rhampholeon bruessoworum
sp. nov.
are summarized in
Table 9
.
TABLE 9.
Measurements (mm) for the type series of
Rhampholeon bruessoworum
sp. nov.
from Mount Inago, Mozambique (PEM: Port Elizabeth Museum).
Sex |
PEM R20375 Holotype F |
PEM R20376 Allotype M |
PEM R20374 Paratype F |
Snout-vent length Tail length Total length |
47.3 14.8 62.1 |
39.0 17.1 56.1 |
47.5 15.3 62.7 |
Head length Head width Orbit diameter |
15.0 9.2 4.4 |
14.5 7.9 4.1 |
15.9 9.7 4.9 |
Snout length Inter-orbital Rostral process |
5.6 6.3 1.6 |
4.8 6.5 2.1 |
5.6 6.8 1.6 |
Casque to Eye |
10.8 |
10.4 |
11.8 |
Diagnosis.
The Mt. Inago Pygmy Chameleon is referable to
Rhampholeon
(subgenus
Rhinodigitum
) by possessing an unpigmented parietal peritoneum, claws that are strongly bicuspid, smooth plantar surfaces, and a rostral process. It can be distinguished from most other species in
Rhampholeon
(
Rhinodigitum
)
by having deep inguinal (absent or indistinct in
Rh. boulengeri
,
Rh. nchisiensis
,
Rh. uluguruensis
, and
Rh. moyeri
) and axillary pits (also absent in
Rh. nchisiensis
). It differs from
Rh. platyceps
and
Rh. maspictus
sp. nov.
in its small size (<
50 mm
SVL), relatively large rostral process in males, and weakly developed crenulations along the dorsal crest. It differs from
Rh. chapmanorum
in having a relatively large rostral process in males (small in both sexes in
Rh. chapmanorum
), and from all other members of the
Rh. platyceps
complex in
Mozambique
(i.e.
Rh. maspictus
sp. nov.
,
Rh. nebulauctor
sp. nov.
and
Rh. tilburyi
sp. nov.
) in having a relatively longer tail in both sexes. From all other
Rhampholeon
it is also genetically well differentiated, and all chameleons examined form a monophyletic clade.
Description of
Holotype
. Adult female, viscera exposed by a single ventral incision.
Head: Dorsum of head flattened, with no upward flexure of the snout; casque flat, edged with weakly-defined lateral crests that are mainly restricted to the posterior region of the casque; temporal crest weakly-developed, comprising a single, interrupted row of large tubercles; parietal crest almost absent, composed of a few enlarged tubercles in the mid-line; supraorbital ridges reduced to a few scattered enlarged scales but with a very small multiscaled process forming a ‘soft horn’ at each end of the inter-orbital ridge that passes across the crown and is composed of 10 small granular tubercles, and that demarcate the posterior edge of a slight frontal depression; inferior orbital rim with 4 (right) and 5 (left) enlarged tubercles; snout bordered on each side by moderately developed rostral crests, that fuse together at the tip of the snout which is adorned with a very small, flattened rostral process (
1.6 mm
) which underneath is only slightly free from the rostral, and is four small tubercular scales long and four tubercular scales wide at its base; nares opening posterio-ventrally; no gular or mental appendages; scales on throat homogenous, more conical but smaller than those on crown of head and subequal in size to those on the belly.
Body: Dorsal crest very weakly developed, reduced to 9 crenulations of enlarged, but not obviously spinose scales; crenulations most strongly developed over mid-body, reduced in size over on neck and which are present on the tail in more reduced form; deep axillary and inguinal pits are present; flank scalation heterogeneous, composed of small, stellate granules with few scattered, enlarged spinose tubercles, the largest at the shoulder and in two clusters; chest, belly and lower surface of tail smooth; limb scalation more tubercular, with a few enlarged, spinose tubercles on the forearms; claws strongly bicuspid; accessory planter spines on the soles of the fore and hind feet are present, but reduced to very small, soft, spinose scales at the base of the claws; tail flattened laterally, flexing downward on the distal third.
Colour in life (based on two images of
holotype
, JB;
Fig. 9
A): Mid-body mottled brown with two narrow, oblique purple-brown lateral stripes; dorsal surface of fore-body, neck, top of head and upper surfaces of limbs darker brown; Throat lightly mottled cream extending onto chin and labials, which have a light yellow flush; belly and base of tail pale brown.
Colour in preservative: Body mottled brown with two narrow oblique reddish-brown bars on mid-flanks; lower surface of neck, belly, base of tail, soles of feet, and lower limbs pale brown.
Description of Allotype
(as for
holotype
, unless noted): Adult male, incision along base of tail with hemipenal muscle removed; hemipenes not everted.
Head: Parietal crest almost absent, composed of a four enlarged tubercles in the mid-line; five enlarged tubercles on both sides of the inferior orbital rim; rostral process six small tubercular scales long and four tubercles wide at base.
Body: Dorsal crest very weakly developed, reduced to nine crenulations of enlarged but not obviously spinose scales, subequal in development to those of the female
holotype
; tail relatively long (30.5% SVL), with a prominent hemipeneal bulge.
Colour in life (based on two images of allotype;
Fig. 9
B): Mid-body mottled brown with small orange brown blotches along dorsal crest, separated by 2–3 crenulations; throat, belly and lower surfaces of limbs and tail pale brown.
Colour in preservative: After preservation body pale brown with vestiges of two narrow oblique stripes on the flanks; pale brown below.
Paratype
variation
(as for
holotype
, unless noted): Adult female with a large ventral incision. The ‘soft horn’ on the supraorbital ridge is very small and hardly protrudes; only four enlarged tubercles on inferior orbital rim; plantar spines very reduced to small, soft, spinose scales.
Size.
Presumably a small species, as all three specimens in the
type
series were sexually mature, with turgid testes or developing ova. Largest male - PEM R20376 (allotype) 39.0 + 17.1 =
56.1 mm
; largest female—PEM R20374 (
holotype
) 47.5 + 15.3 =
62.7 mm
.
Distribution.
Restricted to the
type
locality; Mt. Inago, Zambézia Province, northern
Mozambique
.
Habitat.
The Inago Massif shows habitat zonation, and is surrounded by
Brachystegia
woodland at the base. The
type
series were collected at night in mid-altitude (~
1500 m
) evergreen forest at the base of a granite inselberg (
Fig. 9
C). This forest
type
comprised relatively large trees between
20-30 m
high, with the upper canopy layer composed of species such as
Drypetes natalensis, Schefflera
umbellifera
and
Newtonia buchananii
, whilst the midcanopy layer (<
20 m
) was dominated by
Chrysophyllum gorungosum, Myrianthus
holstii, bridelia
sp. and
Garcinia
sp. These remnant forest patches are greatly reduced in size (<10 ha), fragmented, and highly threatened (Bayliss
et al
. 2010).