A LABORATORY EXPOSURE PROCEDURE FOR SCREENING PULP AND PAPER-MILL EFFLUENTS FOR THE POTENTIAL OF CAUSING INCREASED MIXED-FUNCTION OXIDASE ACTIVITY IN FISH
Ph. Martel et al., A LABORATORY EXPOSURE PROCEDURE FOR SCREENING PULP AND PAPER-MILL EFFLUENTS FOR THE POTENTIAL OF CAUSING INCREASED MIXED-FUNCTION OXIDASE ACTIVITY IN FISH, Environmental pollution, 89(3), 1995, pp. 229-240
To better understand the relationships between pulp manufacturing proc
esses and mixed function oxidase (MFO) enzyme induction in fish, a pra
ctical and standardized exposure procedure is required. This study was
undertaken to develop a laboratory-based exposure procedure to quanti
fy the relative MFO induction potencies of different types of pulp and
paper mill effluents. One major consideration in developing the proce
dure was to ensure that the protocol las practical so that tests could
be performed in a short time, with small volumes of effluents and usi
ng simple experimental conditions. A series of concentration-response
and time-course experiments were conducted to find the minimum time an
d effluent concentration which could distinguish the ability of differ
ent effluents to cause significant MFO induction in rainbow trout in t
he laboratory. Experiments were also conducted to determine the effect
s of biotic and abiotic factors such as loading density, fish size and
feeding regime. This study showed that the exposure of rainbow trout
in the laboratory to 10% concentration of secondary-treated effluent f
or 96 h caused significant increases in hepatic MFO activity. The magn
itude of MFO induction was comparable to other field and laboratory ob
servations. While fish size, lending density and feeding regime were f
ound to affect the test results, consistent responses within a laborat
ory using this protocol are possible, provided that these factors are
standardized. Therefore, the short-term exposure approach described in
this paper could be a relevant tool for assessing the ability of diff
erent types of pulp and paper mill effluents to cause MFO induction in
fish.