V. Smakakincl et al., THE EVALUATION OF WASTE, SURFACE AND GROUND-WATER QUALITY USING THE ALLIUM TEST PROCEDURE, Mutation research. Genetic toxicology testing, 368(3-4), 1996, pp. 171-179
The bulbs of Allium cepa were grown in test liquids of various polluti
on levels as follows: undiluted industrial and municipal waste water;
biological treatment plant output water; water from the Drava river up
stream and downstream of the city of Maribor; and non-chlorinated drin
king water as a negative control test. The paper presents the response
of the Allium cepa genetic material to the presence of potential cyto
toxic and genotoxic substances in test liquids and the suitability of
the Allium cepa testing procedure as a method for short-term determina
tion of water pollution level. The suitability of the Allium test proc
edure as a system for environmental monitoring is presented. The influ
ence of water pollution on macroscopic and cytologic parameters of the
common onion by application of the biological testing method was exam
ined. The macroscopic parameter was inhibition of root growth, The cyt
ological parameters were: aberrant cells in metaphase and anaphase, in
dex of micronuclei appearance and inhibition of cell division. The pos
sibility of categorization the different polluted test liquids into qu
ality classes is presented according to the influence of the test liqu
ids on macroscopic and cytologic parameters. Test liquids are divided
into 8 quality classes: the first class is the least polluted surface
waters, the second and the third classes are more polluted surface wat
ers, the fourth and the fifth classes are biological treatment plant o
utput waters, the sixth till the eighth quality classes are untreated
waste waters, The most polluted test liquids (untreated industrial and
municipal waste waters) caused sublethal and even lethal effects, The
most polluted tested liquids cause the inhibition of root growth over
50% (even up to 74%), decrease of mitotic index over 36% (even up to
66%), increase of presence of interphase cells with micronuclei over 3
% and increase of presence of aberrant cells for more than 10 times in
comparison to control test.