MILIOLIDAE - Acta Palaeontologica Polonica
MILIOLIDAE - Acta Palaeontologica Polonica
MILIOLIDAE - Acta Palaeontologica Polonica
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30 EWA LUCZKOWSKA<br />
Studying the sections of forms, from the juvenile to the adult or<br />
gerontic one, in different species, or observing the developmental stages<br />
of individual specimens, we can arrive at the following conclusions:<br />
1) The size of test does not depend on the number of chambers but,<br />
above all, on the size of the proloculus. The larger the proloculus, the<br />
fewer are the chambers in specimens of the same size or, in other words,<br />
the juvenile stage of the mega I or mega II generation may be the same<br />
size as the adult stage of the micro ~eneration. This is particularly well<br />
seen in the genera marked by the presence of three generation, Le. in<br />
Quinqueloculina, Triloculina and Pyrgo (e.g. Quinqueloculina anagallis,<br />
Text-figs. 7, 8; Q. buchiana, Text-figs. 12, 13; Q. lentica, Text-fig. 18;<br />
Q. parakneriana, Text-fig. 19; Q. pseudobuchiana, Text-fig. 20; Triloculina<br />
neudorfensis, Text-fig. 46).<br />
2) In the genus Quinqueloculina, producing the massiline adult (or<br />
gerontic?) stage (Part I, p. 346) such forms are met with that their membership<br />
in a given species is determined by the quinqueloculine i.e. juvenile<br />
stage only, since the massiline forms of various species closely<br />
resemble each other in shape. For example, Quinqueloculina buchiana MS,<br />
Q. pseudobuchiana MS and Q. haidingeri MS or Q. akneriana MS, Q. triangularis<br />
MS and Q. parakneriana MS are very much alike. At the same<br />
time the quinqueloculine stage is different in each of these species, in<br />
whose populations it besides prevails most frequently (except for Q. haidingeri,<br />
found mostly as MS), owing to which they can be distinguished<br />
without resorting to sections. This can be interpreted in two ways: either<br />
the genus Massilina actually exists and then the various shapes of the<br />
juvenile stage seen in the sections of similar forms indicate their polyphyletic<br />
origin or Massilina represents only an ontogenetic stage of Quinqueloculina,<br />
isomorphic in different species. The latter view has been<br />
assumed in the present work (see Part I).<br />
3) As can be seen from sections, in a number of genera some species<br />
do not differ in their juvenile stage and their individual characters do not<br />
differentiate before several initial chambers have been developed. For<br />
example, in Cycloforina contorta and C. lachesis tubular chambers occur<br />
in the juvenile stage as in C. gracilis and C. lucida (Text-figs 26, 28) and<br />
only in a later stage angular edges appear in C. contorta and C. lachesis,<br />
but not in the other two species. Tubular chambers of the juvenile stage<br />
are also observed in other species which have edges or ribs in the adult<br />
stage: Lachlanella schroekingeri (Text-fig. 33/3, 4), L. undosa (Text-fig.<br />
33/5, 6), Cycloforina badenensis (Text-fig. 25), Triloculina intermedia<br />
(Text-fig. 46/4), T. neudorfensis (Text-fig. 46/3), etc. In the genera Miliolinella<br />
and Varidentella, which are characterized by a turn of the coiling<br />
axis in the juvenile stage, this stage has a similar form in different<br />
species. It resembles Miliolinella circularis in appearance (e.g. in Varidentella<br />
reussi, Part I, PI. XIII, Fig. 3) and is very often identified as that