Didymosphenia populations originating from localities in Siberia/Russi
a (Lake Baikal, River Angara), Pakistan (Himalaya, 3300 m above sea le
vel), Ireland (Killarney) and from the Faroe Islands have been investi
gated in LM and SEM. Other populations from Norway, Sweden, Finland, S
cotland, Russia (Lake Onega, Lake Issyk), Kazakhstan (River Iii), and
Svalbard we compared in LM only. We distinguish 5 taxa at the specific
rank. 1.) Didymosphenia geminata (Lyngb.) M. Schmidt with three, prov
isionally designated morphotypes: geminata sensu stricto, capitata and
subcapitata. 2.) Didymosphenia siberica (Grun.) M. Schmidt (sensu str
icto). 3.) Didymosphenia curvata (Skv. and Meyer) nov. stat. 4.) Didym
osphenia clavaherculis (Ehr.) nov. comb. 5.) Didymosphenia pumila nov.
spec. These taxa are differentiated by the structure of the areolae w
hich is profoundly different in D. geminata and D. clavaherculis compa
red to D. siberica, D. curvata, D. pumila. Nevertheless we do not inte
nd to split the genus on this criterion, despite several recent cases
of hasty splittings by other authors. Our observations are compared wi
th older and more recent literature data, in particular with the numer
ous infraspecific taxa introduced by Skvortzow and Meyer (1928) and Sk
vortzow (1937). The taxa created by the latter authors cannot be disti
nguished from each other. Moreover they do not represent real populati
ons. From the critical biological view of modern taxonomy they should
be seen as typologically described ''pseudo-taxa'' only. Of course aut
hors always select and name single individuals as regular variants of
the cell cycle. However, their studies on Lake Baikal did not reveal t
he 5 real species that occur in 6 to 7 populations, when one takes the
morphotypes (populations) into account. Despite these obvious shortco
mings one of these taxa, D. geminata var. baicalensis fo. curvata is c
hosen as the basionym for a new species: D. curvata. It is shown that
Didymosphenia dentata Dorogostaisky sensu Skvortzow and Meyer should n
ot be regarded as a distinct species or race. It is evidently based on
an optical artefact. Under a certain focus the high profile of the tr
ansapical costae of D. geminata resemble a regular row of spines at th
e junction of the valve face and mantle. Two forms of spines occur in
subapical positions. Continuous spines occur in more weakly silicified
marginal crests in D. geminata and D. clavaherculis. In the other thr
ee species however, completely isolated, more solid and longer spines
occur on the edge of the mantle, without any traces of crests. Apparen
tly they were overlooked (corroded?) by Dawson (1973b).