Review of the millipede tribe Polydrepanini, with the description of a new species from Kerala state, southern India (Diplopoda, Polydesmida, Paradoxosomatidae, Alogolykinae)
Author
Golovatch, Sergei I.
Institute for Problems of Ecology and Evolution, Russian Academy of Sciences, Leninsky pr. 33, Moscow 11907, Russia.
Author
Aswathy, Mathilakath Dasan
0000-0002-3904-8066
Centre for Animal Taxonomy and Ecology (CATE), Christ College, Irinjalakuda, Kerala, India. & aswathym. das 94 @ gmail. com; https: // orcid. org / 0000 - 0002 - 3904 - 8066
aswathym.das94@gmail.com
Author
Bhagirathan, Usha
Author
Sudhikumar, Ambalaparambil Vasu
0000-0002-4479-4995
Centre for Animal Taxonomy and Ecology (CATE), Christ College, Irinjalakuda, Kerala, India. & spidersudhi @ gmail. com; https: // orcid. org / 0000 - 0002 - 4479 - 4995
spidersudhi@gmail.com
text
Zootaxa
2021
2021-11-18
5068
4
485
516
journal article
3396
10.11646/zootaxa.5068.4.2
45ebb61b-259d-4ac3-bd7c-3a7da0f644f5
1175-5326
5709510
F769B986-8F7B-4ABF-A7EF-58A813718760
Delarthrum anomalans
sp. nov.
Figs 69–87
.
Material examined.
Male
holotype
(CATE-61604A),
2 male
(CATE-61604B and CATE-61604C) and
2 female
paratypes
(CATE-61604D and CATE-61604E),
India
,
Kerala state
,
Thrissur district
,
10°21’19’’N
,
76°12’48’’E
,
29 m
a.s.l.
,
in
June 2021
and
1 male
(CATE-61604J) and
2 female
paratypes
(CATE-61604K and CATE-61604L all in 5302B–CATE-5302I) from the sacred groves of
Valliyur
kavu,
Manathavady
,
Wayanad district
,
11°48’08’’N
,
76°01’55’’E
,
716 m
a.s.l.
,
M.D. Aswathy
leg.
Name
. To emphasize the anomalous absence of adenostyles from both male legs 1 and 2.
Diagnosis
. Differs from congeners by the absence of adenostyles from both male legs 1 and 2, coupled with the sexually dimorphic colour pattern, the transverse tergal sulci starting with the collum, and the peculiar gonopodal conformation, primarily the presence of a small, thumb-shaped, distoventral projection (
a
) basal to the division of the postfemoral part into (1) the main, dorsal piece of the solenophore (
sph
), which is long, obliquely truncate dorsad at the base, bifid in the distal third and slightly curved mesad, and (2) a dorsal process that is split immediately at the base into a longer, stalked, leaf-shaped outgrowth (
b
) with peculiar, ragged, saw-like distal margins, and a much shorter, simple, dorsobasal peg (
z
) (
Figs 84–87
).
FIGURES 69–73.
Delarthrum anomalans
sp. nov.
,
paratypes.
69
. Live male in the field, dorsal view (photographed not to scale).
70, 71
. Habitus, fixed male and fixed female, respectively, lateral views.
72, 73
. Fixed male, anterior and posterior parts of body, respectively, dorsal view.
Description
. Length of
holotype
, 17.9 mm, of
paratypes
, 17.0–17.6 mm (male) or 14.0–14.8 mm (female). Width of midbody rings, 2.6 mm (
holotype
), 1.9–2.1 mm (male
paratypes
) or 2.0–2.3 mm (female
paratypes
). Coloration sex-dimorphic:
in vivo,
dorsum dark brown to black, venter chestnut brown (male) (
Figs 69, 70
) to yellowish white (female) (
Fig. 71
); paraterga mostly contrasting pale. Legs light brown (male) or whitish (female). Coloration after one month of preservation in 96% ethanol somewhat darkened, but pattern evident (
Figs 69–76
).
Body with 20 rings in both sexes. In width, collum <head <ring 2<3<4<5<6<7<8<9=10, body gradually tapering thereafter (
Figs 72, 73
). Vertex glossy and bare; stipes, cardo and clypeus moderately setose, epicranial sulcus distinct and ending before the level of antennal sockets. Clypeal region with
ca
5+5 setiferous pits. Antennae moderately long, only slightly clavate, extending back to ring 4 when stretched caudolaterally (
Figs 72
,
74
). Relative antennomere lengths: 1<6<4<2<5<3. Antennomere 6 broadest apically, post-antennal groove shallow, diameter of antennal socket and isthmus between sockets subequal, 0.24 and 0.23 mm, respectively (
Fig. 77
). Antennomeres 5–7 each with a distinct dorso-apical group of basiconic sensilla (both male and female), these being especially conspicuous on antennomere 5 (
Figs 72
,
74
).
Paraterga mostly well developed, keel-shaped, set at about upper third of body height (
Figs 69–76
). Collum ovoid, paraterga small, subtriangular and broadly rounded. Anterior margin of collum with a single transverse row of fragile short setae (
Fig. 72
). Anterior and posterior margins of following rings rather straight and parallel. Anterior margin with a transverse row of 2+2 short setae similar to those on collum. Paraterga 2 as usual, set clearly lower than 3
rd
, squarish in shape, anterior corner/lobe drawn anteriad. Following paraterga 3–17 regularly rounded anterolaterally and increasingly drawn caudolaterad into acute triangles, but still lying within rear tergal margins (
Figs 72–76
),
vs.
small, spiniform and slightly drawn past rear tergal margin on rings 18 and 19 (
Figs 73
,
76
). Lateral calluses of paraterga thin, only slightly thicker on pore-bearing rings than on poreless ones (
Figs 69, 70
), smooth, delimited by distinct sulci both dorsally and, to a lesser degree, ventrally; usually with a few short setae retained at lateral margin.
Tegument generally smooth and shining, prozonae very delicately shagreened, metazonae mostly striate/striolate at bases of paraterga and near transverse sulci, surface being slightly undulate (
Figs 72, 73
). Tergal setae mostly short and inconspicuous, present both on paraterga and in anterior half of metaterga. Two deep transverse sulci present on collum (
Fig. 72
), followed by one prominent sulcus on metazonae 2–18, smooth at bottom and reaching the base of paraterga (
Figs 72, 73
). A faint axial line traceable on most metazonae until 18
th
(
Figs 72, 73
). Strictures between pro- and metazonae narrow, nearly smooth, at most faintly striolate (
Figs 72–76
).
Pore formula normal (5, 7, 9, 10, 12, 13, 15–19), ozopores small, circular, opening at
ca
1/3 off caudolateral corner of pore-bearing calluses (
Figs 74–76
). Pleurosternal carinae decreasing in size from 2 to 4. Epiproct conical and flattened dorsoventrally, extending well beyond anal valves; tip truncate, subapical lateral incisions evident; hypoproct subtriangular, with 1+1 setae on minute knobs (
Fig. 79
).
Legs moderately long and slender, clearly longer and thickened in male compared to female (
Figs 70, 71
), rather densely setose ventrally and with short claws; male legs with tarsal brushes absent only from last two leg-pairs (
Figs 74–76, 78
,
83
). Prefemora and coxae each bearing a moderately long and stiff distoventral seta. Podomere length ratios: coxa <prefemur <tibia = postfemur <tarsus <femur (
Fig. 83
). Neither male leg-pair 1 nor 2 with any adenostyles, only coxae 2 as usual, with gonopores on small knobs (
Figs 81, 82
). Sternal lobe between male coxae 4 small, conical and densely setose.
Gonopodal aperture transverse and suboval in shape, about 2/3 as wide as prozonite 7, its rim being not elevated, but thickened laterally (
Fig. 78
). Gonopods high, complex,
in situ
held parallel to each other (
Figs 78, 80
). Coxite darkened, about as long as femorite, subcylindrical, setose distoventrally (
Figs 84–87
); cannula a short curved tube, as usual. Prefemoral part short, globose, densely setose as usual, with a particularly long seta distoventrally. Femorite (
fe
) relatively stout and short, somewhat enlarged distad, subclavate, almost as long as acropodite (= postfemoral part), subcylindrical, without evidence of torsion; a small, thumb-shaped, distoventral projection (
a
) basal to acropodite bifurcation into a longer, larger, more slender, subacuminate, ventral, solenophore branch (
sph
), rather slightly curved dorsad and bearing both a strong spine (
k
) in distal third and a free solenomere (
sl
), and a shorter, more elaborate, dorsal process divided immediately at base into a longer, stalked, leaf-shaped outgrowth (
b
) with peculiar, ragged, saw-like distal margins, and a much shorter, simple, dorsobasal peg (
z
). Seminal groove first running all along mesal side of femorite, then turning slowly towards bifurcation point before moving onto a free, flagelliform
sl
tightly attached to mesal side of
sph
, with only a short tip of
sl
remaining exposed over
sph
. Division of
fe
and acropodite through a transverse sulcus, or of
sph
into laminae, wanting (
Figs 84–87
).