Na. Filippova, VENTRAL SKELETON OF MALE OF IXODID TICKS OF THE SUBFAMILY AMBLYOMMINAE, ITS EVOLUTION AND ROLE FOR SUPERGENERIC TAXONOMY, Parazitologia, 27(1), 1993, pp. 3-18
A comparative study of the ventral skeleton of idiosoma of male of the
subfamily Amblyomminae was carried out. Much prominence was given to
the hind half of idiosoma: great diversity of the composition, shape,
size and topography of integumentary hard elements. A comparative stud
y of the topography of dorsoventral musculature attachment to the vent
ral wall of idiosoma in its hind half was carried out, too. The struct
ure of skeleton with the largest area and least differentiation should
be considered most primitive; in this case all hard elements have no
distinct species or group form and are attached rigidly to the extensi
ble cuticle. Such structure is characteristic of Haemaphysalis (Alloce
rea) inermis which has primary unpaired anal and paired postanal shiel
ds occupying nearly the whole ventral surface of the hind half of idio
soma (fig. 1, 1). This variant suggests the other ones characteristic
of the subfamily Amblyomminae. Two types of evolutionary transformatio
ns of hard ventral integuments of male have been revealed. One type re
presents a successive process of skeleton reduction through disintegra
tion of primary shields into numerous small ones and decrease of their
sizes and number up to their complete disappearance (figs. 1, 2). Har
d elements are preserved for the most long time on hind branches of th
e genital groove. Continuous chains of bundles of dorsoventral muscula
ture, running along hind branches of the genital groove, are attached
to hard elements and reach the posterior end of idiosoma between scall
ops II and III (fig. 5). In H. (Allocerea) inermis muscles are attache
d to the primary paired postanal shields, and where a partial skeleton
reduction took place - to derivatives of these shields. The shields o
r their derivatives have no species or group form, are asymmetrical an
d attached rigidly to extensible integuments; the number of derivative
sclerites varies much. A complete reduction of the ventral skeleton m
arks the top of this evolutionary trend. In this case the topography o
f musculature attachment is preserved (fig. 5). During evolutionary tr
ansformations of the other type the primary postanal shields along the
line of hind branches of the genital groove broke into adanal and acc
essory ones, and their medial and lateral divergence took place (figs.
3, 4). Later on, in some recent genera the skeleton underwent a parti
al reduction at the expense of the decrease of the above shields in ar
ea, or complete disappearance of the accessory ones (figs. 3, 2; 4-6).
On the contrary, in the other genera the area of hard integuments enl
arged on account of the growth or increase in the number or shields (f
ig. 4). If the transformations are estimated by the character of hard
integuments area, then their initial stage is close to the area in H.
(Allocerea) inermis (figs. 3, 1, 3). But this type of transformations
lacks a complete reduction of ventral skeleton. The topography of atta
chment of the bundles of dorsoventral musculature to the ventral wall
of idiosoma is characterized by the branching from the genital groove
to adanal and accessory shields and the bundles do not reach marginal
scallops (fig. 6). All the shields have a distinct species or group fo
rm and number; the connection with extensible integuments is semimobil
e. The two types evolutionary transformations of the ventral skeleton
of idiosoma in male with characteristic topography of musculature atta
chment enable us to place two tribes in the subfamily Amblyomminae Ban
ks, 1907. The tribe Amblyommini Banks, 1907 includes the genera Haemap
hysalis Koch, 1844, Amblyomma Koch, 1844, Aponomma Neum., 1899, Anomal
ohimalaya Hoog., Kaser et Mitch., 1970, Dermacentor Koch, 1844, Rhipic
entor Nutt. et Warb., 1908. The tribe Rhipicephalini Banks, 1907 inclu
des the genera Rhipicephalus Koch, 1844, Hyalomma Koch, 1844, Cosmiomm
a Schulze, 1919, Nosomma Schulze, 1919, Boophilus Cur., 1891, Margarop
us Karsch., 1897.