Electronic Journal of Polish Agricultural Universities (EJPAU) founded by all Polish Agriculture Universities presents original papers and review articles relevant to all aspects of agricultural sciences. It is target for persons working both in science and industry,regulatory agencies or teaching in agricultural sector. Covered by IFIS Publishing (Food Science and Technology Abstracts), ELSEVIER Science - Food Science and Technology Program, CAS USA (Chemical Abstracts), CABI Publishing UK and ALPSP (Association of Learned and Professional Society Publisher - full membership). Presented in the Master List of Thomson ISI.
2008
Volume 11
Issue 4
Topic:
Fisheries
ELECTRONIC
JOURNAL OF
POLISH
AGRICULTURAL
UNIVERSITIES
Czerniawski R. 2008. ZOOPLANKTON EXPORTED FROM RETENTION RESERVOIRS AT THE POST-PRODUCTION WASTE WATER TREATMENT PLANT, EJPAU 11(4), #18.
Available Online: http://www.ejpau.media.pl/volume11/issue4/art-18.html

ZOOPLANKTON EXPORTED FROM RETENTION RESERVOIRS AT THE POST-PRODUCTION WASTE WATER TREATMENT PLANT

Robert Czerniawski
Department of General Zoology, University of Szczecin, Szczecin, Poland

 

ABSTRACT

In the years 2002 and 2003 the zooplankton from the outflows from two retention reservoirs, characterised by different biological conditions, at the sewage treatment plant in the area of the Chemical Plant Police was studied. One reservoir was in 70% grown with vegetation, mainly submerged species and hosted fish, while the other had no fish and its bottom was covered only in 10% by emerged vegetation. Cyclic appearance of certain zooplankton species was noted; particularly interesting was increasing abundance of Daphnia magna in warm seasons. The outflows from the second reservoir contained a greater number of taxa and greater abundance and biomass of zooplankton, however, the difference was not statistically significant (p < 0.05).

Key words: artificial reservoirs, Daphnia magna, outflows, water plants, zooplankton.

INTRODUCTION

It is known that small water reservoirs undergo eutrophication relatively fast. Their small area and low depth favour this process accompanied by abundant development of zooplankton. Chemical and biological characteristics of small water reservoirs localised far from human habitation sites are comparable to those in larger reservoirs, however, when they are subjected to considerable anthropogenic pressure the chemical composition of their water can be determined by the limiting element. The polluted and strongly eutrophicated environment is particularly favoured by some species of Rotifera whose abundance can reach a few thousand in L [13,17,31]. Often they belong to the ubiquistic species highly tolerant towards environmental factors [29]. High fertility of water is also a factor permitting the occurrence of large forms of plankton crustaceans, on condition of the absence of fish in a given reservoir. The reservoirs showing considerable development of eutrophication and relatively high abundance and biomass of the zooplankton are, among others, the retention ones at the sewage or waste-water treatment plants and small size artificial and natural reservoirs.  Szlauer [23] studied the quantitative and qualitative composition of the zooplankton in the retention reservoir at the waste-water treatment plant at the Chemical Plants in Police, and reported great abundance and biomass of the zooplankton with a particularly significant contribution of large Cladocerans Daphnia magna. Similarly, in the sedimentation tanks of the sewage treatment plant in Drawno (NW Poland), in late spring, high concentrations of zooplankton were reported [4]. Similarly high abundances of zooplankton have been found in small lakes and ponds surrounded by arable fields, the water of these reservoirs contains relatively high amounts of phosphorus and nitrogen. Demetraki-Paleolog [5] reported the occurrence of Rotifers in the abundances up to 7000 individuals per L in shallow and small lakes.

The aim of the study was a comprehensive analysis of the zooplankton in the outflows of the waste-water treatment plant, in particular determination of its species composition, abundance, seasonal changes and the differences in the zooplankton in two reservoirs of different biological conditions.

In view of the established high abundances of plankton crustaceans in artificial reservoirs, it seemed interesting to analyse the zooplankton carried in the outflow from two retention reservoirs at the waste-water treatment plant at the Chemical Plant Police.

MATERIAL AND METHODS

The zooplankton was analysed in the outflows from two retention reservoirs at the waste-water treatment plant at the Chemical Plant Police. The outflows from the reservoirs 1 and 2 were denoted as Outflow 1 (site 1) and Outflow 2 (site 2) discharge into the Jasienicki Canal joining them directly with the Szczecin Bay. Reservoir 1 occupies the area of 40 ha, has a maximum depth of 2 m, and is in about 70% covered with plants, both submerged and emerged. Almost all along the west shore there are 22 pipes discharging the post-production waste-water from the Chemical Plants obtained after the production process of three-component mineral fertilisers, phosphoric and sulphuric acids, fluorine compounds, titanium white, ammonia and urea.  The temperature of the waste-water released from the plant is 40°C and its pH varies from 1 to 2. The post-production waste-water is directed to the chemical and mechanical purification plant at which phosphates are precipitated. At the next stage the waste water is decanted in Dorr sediment tanks and the process is accelerated by addition of flocculants. From the sediment tanks the water is flown to the retention reservoir. Prior to reaching the outflow the water is directed to pass through three dikes, dividing the reservoir into a few basins. The water is discharged from the reservoir through concrete pipes of 120 cm in diameter localised after the diversion weir on the south shore of the reservoir [29]. The location and map of retention reservoir 1 with marked sites of sample collection is shown in Fig. 1.

Fig. 1. Map of retention reservoir 1 at the post-production waste water processing plant at the Chemical Plant Police with a marked site 1 of sample collection – outflow 1

Retention reservoir 2 has been founded on the basis of the earlier natural pond supplied by ground water and precipitations. It is the last element of the post-production waste-water treatment plant in the Chemical Plant Police, in which the water subjected earlier to mechanical and chemical cleaning is biologically purified. Reservoir 2 occupies the area of about 40 ha and its depth reaches 3 m at the waste water inflow and 1 m at the discharge to the Jasienicki Canal, and is grown in about 10% with emerged plants. In the reservoir there are three dikes prolonging the flow of water and hence the time of retention. The reservoir hydrology is controlled by the inflow of waste-water and partly by precipitations. The water temperature in reservoir 2 is relatively high and in summer reaches even 31ºC, so it is higher than the temperatures of natural surface water in the same period [22]. The outflow occurs through three metal pipes of 70 cm in diameter. The location and map of retention reservoir 2 with marked site of sample collection is shown in Fig. 2.

Fig. 2. . Map of retention reservoir 2 at the post-production waste water processing plant at the Chemical Plant Police with a marked site 2 of sample collection – outflow 2

The observations were carried out in the years 2002–2003. The samples of zooplankton were collected every month at the sites marked on the maps (except January and December 2002). At each site and each time two samples were collected: for the quantitative study by filtering 100 L of water through the mill gauze of the mesh size 50 µm and for the qualitative study by placing the mill gauze of the mesh size 50 µm in the water current for 10 minutes. Depending on the density of zooplankton the volume of the sample was reduced to 10 – 80 cm3, from which 1 mL was collected to the chamber and analysed. The count was at least three times repeated and performed of the individuals representing particular systematic groups of crustaceans, the species were identified and the individuals of rotatoria were counted. The abundance of zooplankton was expressed per 1 L. In order to find the abundance of species represented by large individuals, occurring often in small numbers, the volumes of the whole samples were analysed. In each sample the lengths of at least 30 individuals from each species represented were measured. The data were used for calculation of the biomass of the zooplankton and the so-called wet mass of the zooplankton carried out with the outflow in kg per day.

The weight of the animals was calculated from their lengths on the basis of the tables proposed by Morduchaj-Bołtovskoj [21] and Starmach [27]. The species were identified with the help of the keys prepared by Wagler [32], Kutikova [17], Kiefer and Fryer [12], Rybak [23,24].

The taxonomic similarity between the sites was calculated according to the formula of  Marczewski and Steinhaus [19]:
S = W/A + B – W

Where:
S – is the statistical similarity between the two sites compared,
A – is the number of elements in set,
A, B – is the number of elements in set B,
W – is the number of elements common for sets A and B.

The data on abundances and biomass of the zooplankton were subjected to statistical analysis with the help of the software Excel and Statistica. The hypothesis of the equality of the mean values was verified after prior testing the normalcy of distribution of the feature analysed (Shapiro-Wilk test) and the Levene test of homogeneity of variance.  The significance of differences was determined by the Scheffe test (p<0.05) and variance analysis (W) (for many samples) [26].

RESULTS

The species composition and frequency of zooplankton at the sites of study are presented in Tables 1 and 2. At the outflows from retention reservoirs 1 and 2, at the both sites the number of taxa noted was 30 and 33, with 21 and 26 species, respectively. The most often represented were: nauplius Cyclopoida, kopepodit Cyclopoida, Acanthocyclops robustus, Eucyclops serrulatus, Daphnia magna, Brachionus angularis, Brachionus calyciflorus, Brachionus variabilis, Keratella cochlearis, Keratella quadrata, Polyarthra sp. The occoncurence and abundance of some zooplankton components was definitely seasonal. The most important species with cyclic presence at site ZbR 1 included: A. robustus, E. serrulatus, Cyclops vicinus, D.a magna, Ceriodaphnia quadrangula, Brachionus angularis, B. variabilis, Keratella quadrata, Polyarthra sp., Notholca squamula. At site ZbR2 the most important cyclically appearing species were: A. robustus, D. magna, B. angularis, B. calyciflorus, B.s variabilis, K. quadrata. At both sites K. quadrata appeared only in colds seasons.

As to the frequency of the taxa at site 1 it was found that only representatives of Nauplii Cyclopoida were present in 100% of the qualitative samples throughout the period of the study. The frequency of 80% was established for the three taxa: including Copepoda, Copepodites Cyclopoida (95%) and Rotifera non det. (95%). No taxa were characterised with a frequency from the range 60–80%. Only Polyarthra sp. was characterised with a frequency from the range 40–60% , while seven taxa occurred with frequencies from the range 20–40%, including B. variabilis (36%), Asplanchna sp., K. cochlearis i K. quadrata (32%). Twenty taxa were characterised with a frequency below 20%, of which the highest frequency of 18% was found for A. robustus, E. serrulatus and Brachionus urceus.

Table 1. Qualitative composition and frequency of zooplankton recorded in 2002–2003 in outflow from first basin – site 1

Taxons

2002

2003

II

III

VI

V

VI

VII

VIII

IX

X

XI

I

II

III

IV

V

VI

VII

VIII

IX

X

XI

XII

Nauplii Cyclopoida

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

Copepodites Cyclopoida

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

 

x

Copepodites Calanoida

x

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Acathocyclops robustus (Sars)

 

 

 

 

 

 

x

 

 

 

 

 

 

x

x

x

 

 

 

 

 

 

Diacyclops bicuspidatus (Claus)

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Eucyclops serrulatus (Fischer)

 

 

 

 

 

 

x

 

 

 

 

 

 

 

x

 

 

x

x

 

 

 

Cyclops vicinus Uljanin

 

 

 

 

x

 

 

 

 

 

 

x

 

x

 

 

 

 

 

 

 

 

Thermocyclops crassus (Fischer)

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

x

x

 

 

 

 

Thermocyclops oithonoides (Sars)

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

Daphnia cucullata Sars

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Daphnia longispina O.F. Müller

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Daphnia magna Straus

 

 

 

 

 

x

x

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

Daphnia juv.

 

 

 

 

 

x

x

 

 

 

 

 

 

 

 

 

 

x

x

x

x

 

Bosmina coregoni Baird

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

Ceriodaphnia quadrangula (O.F. Müller)

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

x

 

 

 

Chydorus gibbus (Liljeborg)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

Chydorus sphaericus (O.F. Müller)

 

 

 

 

 

 

 

x

x

 

 

 

 

 

 

 

 

 

 

 

 

 

Asplanchna sp. Gosse

x

x

x

 

x

 

 

x

 

 

 

 

 

x

 

 

 

 

x

 

 

 

Brachionus angularis Gosse

 

 

 

x

x

 

 

 

 

 

 

 

 

 

x

x

x

 

 

 

 

 

Brachionus calyciflorus Pallas

 

 

 

x

 

 

x

 

x

x

 

x

x

 

 

 

 

 

 

 

 

 

Brachionus variabilis Hempel

 

 

 

 

x

x

x

 

 

 

 

 

 

x

x

 

x

x

x

 

 

 

Brachionus urceus (Linnaneus)

 

 

 

x

 

 

 

 

 

 

 

 

 

 

x

 

x

 

 

x

 

 

Kellicottia longispina (Kellicott)

 

 

 

 

 

 

 

 

 

 

 

x

x

 

 

 

 

 

 

 

x

 

Keratella cochlearis (Gosse)

 

 

x

x

x

 

 

 

 

x

 

 

 

 

 

 

 

 

x

x

x

 

Keratella quadrata (Müller)

x

 

 

 

 

 

 

x

x

x

x

x

 

 

 

 

 

 

 

 

 

x

Notholca acuminata (Ehrenberg)

 

 

 

 

 

 

 

 

 

 

 

 

x

x

 

 

 

 

 

 

 

x

Polyarthra sp. Ehrenberg

 

 

 

 

x

x

x

x

x

 

 

 

 

 

 

x

x

x

x

x

x

 

Synchaeta sp. Ehrenberg

 

 

x

x

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Notholca squamula (Müller)

 

 

x

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

Rotatoria non det.

x

x

x

x

x

x

x

x

x

x

x

x

x

x

 

x

x

x

x

x

x

x

Table 2. Qualitative composition and frequency of zooplankton recorded in 2002–2003 in outflow from second basin – site 2

Taxons

2002

2003

II

III

VI

V

VI

VII

VIII

IX

X

XI

I

II

III

IV

V

VI

VII

VIII

IX

X

XI

XII

Nauplii Cyclopoida

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

Copepodites Cyclopoida

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

x

 

x

x

x

x

x

Acathocyclops robustus (Sars)

 

 

 

 

x

x

 

x

 

 

 

 

 

 

x

x

 

x

 

 

 

 

Diacyclops bicuspidatus (Claus)

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Eucyclops macrurus (Sars)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

x

 

Eucyclops serrulatus (Fisher)

 

 

 

 

x

x

x

 

 

 

 

 

 

 

x

 

 

 

x

 

 

x

Cyclops strenuus (Fisher)

x

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

 

Cyclops vicinus Uljanin

 

x

 

x

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

Mesocyclops leuckarti Claus

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

Thermocyclops crassus (Fisher)

 

 

 

x

x

x

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Thermocyclops oithonoides (Sars)

 

 

x

x

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

Alona costata Sars

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

Daphnia cucullata Sars

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Daphnia magna Straus

 

 

 

 

x

x

x

x

x

 

 

 

 

 

x

 

x

x

x

x

x

 

Daphnia juv.

 

 

 

 

 

x

 

x

x

 

 

 

 

x

 

 

x

x

x

x

x

 

Bosmina coregoni Baird

 

 

 

 

 

 

 

x

 

 

x

x

x

 

 

 

 

 

 

 

 

x

Chydorus gibbus (Liljeborg)

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

Chydorus sphaericus (O.F. Müller)

 

 

 

 

 

 

 

 

 

x

 

 

 

 

x

 

 

 

 

 

 

 

Asplanchna sp. Gosse

 

 

 

 

 

 

 

x

x

 

 

 

 

 

 

 

 

 

 

 

 

 

Brachionus angularis Gosse

 

 

 

x

x

 

 

 

 

 

 

 

 

 

x

x

x

x

x

 

 

 

Brachionus bidendata Anderson

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

Brachionus calyciflorus Pallas

 

x

x

x

x

 

 

 

x

x

x

x

x

 

 

 

 

 

x

x

 

 

Brachionus variabilis Hempel

 

 

x

x

 

 

x

x

 

 

 

 

 

x

x

 

 

 

x

 

 

 

Brachionus ureus (Linnaeus)

 

 

 

x

 

 

 

 

 

 

x

 

 

 

 

 

 

 

x

x

 

 

Brachionus rubens Ehrenberg

 

 

 

x

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

Filinia longiseta (Ehrenberg)

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

 

Kellicottia longispina (Kellicot)

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

Keratella cochlearis (Gosse)

 

 

 

x

 

 

 

x

 

 

 

x

 

x

x

 

x

 

x

x

x

x

Keratella quadrata (Müller)

x

 

 

x

 

 

 

x

x

x

x

x

x

x

x

 

 

 

 

 

x

x

Notholca acuminata (Ehrenberg)

 

 

 

 

 

 

 

 

 

 

 

 

 

x

 

 

 

 

 

 

x

x

Polyarthra sp. Ehrenberg

 

 

 

 

x

x

x

x

x

 

 

x

 

 

 

x

x

x

x

 

 

x

Synchaeta sp. Ehrenberg

 

x

x

 

 

 

 

 

x

 

 

 

 

 

 

 

 

 

 

 

 

 

Rotatoria non det.

 

x

 

x

 

 

x

x

x

x

x

x

 

x

x

x

x

x

x

x

 

x

At site 2 only Nauplii Cyclopoida were present in all qualitative samples (100% frequency) throughout the period of study. A frequency from the range above 80% was found for the above group and for Copepodites Cyclopoida (95%). Only Rotifera non det., was noted with  a frequency from the range 60–80%, (73%). In the range 40–60% were the frequencies of appearance of K. quadrata (55%), Polyarthra sp. (50%), D. magna (50%), B.s calyciflorus (50%), K. cochlearis (45%) and Daphnia juv. (45%). Five taxa were noted with frequencies from the range 20–40%, including B. variabilis (36%), B. angularis. Twenty taxa were found with frequencies below 20%, with the highest frequency of 18% for B. urceus.
A greater number of species was observed in summer.
The taxonomic similarity between the two sites was 0.7, and the number of common taxa was 28.

The data describing the abundance of zooplankton are collected in Table 3 and shown in Fig. 3. The mean number of plankton animals at site 1 in the whole period of study was 104.33 ind.·L, varying from 0.65 ind.·L in December 2003 to 1021.00 ind.·L in May 2003, which was the peak abundance at this site. The mean number of plankton animals at site 2, throughout the period of study was 286.36 ind.·L, varying from 9.10 ind.·L  in December 2003 to 2089.80 ind.·L in May  2003, at the peak abundance. At both sites the dominant was Copepoda, whose representatives were found at the highest density of 1009.00 ind.·L  at site site 1 (in May 2003), which made over 98% of the zooplankton abundance at this site at that time. Often the domination of Copepoda was a consequence of a high abundance of Nauplii Cyclopoida, often making over 50% of total zooplankton abundance, and in May 2003 at site site 1 the contribution of this taxon to total abundance was over 97%. Along with Copepoda also Rotifera, were represented in the abundances in certain months exceeding 50% of the total zooplankton found. The most abundantly represented was the genus Brachionus, in May 2002 at site 2 dominant over other rotifers (B. angularis 1653 ind.·L, which was almost 90% of the abundance of Rotifera, B. variabilis 208.8 ind.·L, B. urceus 84.6 ind.·L. Cladocera was represented with the lowest abundances. The mean density of Cladocera was even by over 100 lower than the mean abundance of other systematic groups at the same site. The highest abundance of Cladocera was noted in August 2003 at site 2 (71.00 ind.·L), when they were mainly represented by Daphnia magna and juvenile stages of Daphnia sp. In this month D. magna was a definite dominant making over 82% of the zooplankton found at this site. Other species of Cladocera were represented by a low number of individuals. No statistically significant differences in the abundance of zooplankton were found between the sites, (p<0.05). In 2002 the standard deviation values were relatively low, which testifies to small differences between the samples, whereas in 2003 the differences between the samples were considerable.

Table 3. Average (x), scope of value (s) and standard deviation (SD) of abundance [ind.·L], biomass [mg·L] and biomass flow [kg·day-1] of zooplankton in examined sites in 2002 and 2003
 

ZbR 1

ZbR 2

2002

2003

2002–2003

2002

2003

2002–2003

ind. L

Copepoda

x
s
SD

29.9
1.8-104.7
36.2

132.2
0.2-1009.0
311.9

85.7
-
232.8

126.1
1.8-399.6
148.7

45.2
6.7-244.8
66.9

82.5
-
116.6

Cladocera

x
s
SD

1.7
0.3-9.9
3.52

0.7
0.1-7.0
2.0

1.2
-
2.7

6.4
0.4-46.5
14.4

10.7
0.1-71.0
20.4

8.7
-
17.6

Rotifera

x
s
SD

26.8
1.2-91.2
33.5

9.2
0.2-35.6
10.0

17.2

24.8

172.9
0.1-659.7
235.9

2267
2.3-1844.4
521.2

198.3

407.9

Total

x
s
SD

66.3
3.0-196.2
66.8

150.2
0.6-1021.0
313.2

104.3

234.7

360.0
28.8-1059.3
328.0

280.7
9.1-2089.8
581.0

286.3

472.8

mg L

Copepoda

x
s
SD

0.36
0.01-1.69
0.68

0.16
0.01-0.99
0.31

0.25
-
0.50

0.89
0.03-1.75
0.97

0.48
0.01-4.09
1.17

0.68

1.08

Cladocera

x
s
SD

0.16
0.01-0.95
0.34

0.01
0.01-0.07
0.02

0.08
-
0.24

1.05
0.01-6.97
2.16

2.47
0.01-1749
5.07

1.75

3.98

Rotifera

x
s
SD

0.02
0.001-0.07
0.02

0.01
0.01-0.11
0.03

0.02

0.02

0.12
0.01-0.32
0.13

0.17
0.01-1.15
0.32

0.15

0.25

Total

x
s
SD

0.60
0.01-2.59
0.902

0.212
0.01-1.01
0.33

0.37

0.66

202
0.10-8.66
2.56

3.01
0.02-17.49
5.01

2.51

4.03

kg day-1

Copepoda

x
s
SD

20.57
0.02-112.07
39.62

8.31
0.01-54.53
17.03

13.88

29.39

34.09
1.68-125.38
43.70

26.94
0.02-156.66
54.18

30.19

48.68

Cladocera

x
s
SD

9.92
0.82-51.7
20.30

0.71
0.01-5.31
1.62

4.89
-
14.14

43.04
0.24-337.97
104.32

72.87
0.10-655.15
188.04

59.31
-
153.02

Rotifera

x
s
SD

1.04
0.01-4.91
1.59

1.09
0.01-5.27
1.60

1.06
-
1.56

5.42
0.01-14.77
5.74

5.80
0.02-44.47
12.46

5.63

9.77

Total

x
s
SD

34.31
0.06-161.88
53.09

11.43
0.05-55.93
17.88

19.84

38.66

82.54
5.39–412.58
124.60

106.00
2.73–655.48
185.17

95.12

157.33

Fig. 3. The zooplankton abundance [ind.·L] at the sites studied in 2002 and 2003

The data on biomass of the plankton animals are collected in Table 3 and graphically shown in Fig. 4. The mean biomass of zooplankton at site 1 throughout the period of study was 0.3779 mg·L, varying from 0.0009 mg·L in November 2003 to 2.5947 mg·L in August 2002, while at site 2 the mean biomass of zooplankton in the period of study was 2.5150 mg·L, varying from 0.0177 mg·L in December 2003 to 17.4995 mg·L in August 2003. At both sites the main contribution to biomass came from Cladocera, when present. The contribution of Cladocera was the most pronounced at site 2 in August 2003, when the contribution of D. magna reached over 98%. This species was at that time represented  by 17.4995 mg·L. In July 2002 D. magna occurring in the abundance of 6.7722 mg·L made over 78% of biomass of all zooplankton found. Much lower was the biomass of adult forms of Copepoda, although they brought a considerable contribution to the zooplankton biomass on the absence of Cladocerans. The biomass of the representatives of such species as A. robustus, C. vicinus, Thermocyclops crassus and Thermocyclops oithonoides reached high values, almost always over 50% of the total biomass of the zooplankton found. Rotifera had insignificant effect on the biomass of zooplankton, and their contribution was the greatest in May 2003 at site 2, mainly because of high abundance of B. angularis, reaching 0.8200 mg·L and making almost 16% of the total biomass of the zooplankton found and over 71% of the biomass contribution of all Rotifera.

Fig. 4. The zooplankton biomass in [mg·L] at the sites studied in 2002 and 2003

In the whole period of study the biomass values showed no statistically significant differences between the sites (p<0.05). The standard deviation did not differ from the average as much as the values of abundance, which indicates lower differentiation of biomass in the samples studied.

The data on biomass flow of the zooplankton are shown in Table 3 and Fig. 5. The flow of biomass of zooplankton is correlated with the values of biomass and the differences between these parameters stem from different values of the water flow in the outflows from the retention reservoirs. The mean flow of biomass at site 1, throughout the period of study was 19.84 kg·day-1, varying from 0.05 kg·day-1 in November 2003 to 161.88 kg·day-1 in August 2002. At site 2 the mean flow in the period of study was 95.12 kg·day-1, varying from 2.73 kg·day-1 in January 2003 to 655.48 kg·day-1 in August 2003. Similarly as the value of biomass, also the flow of biomass was determined by crustaceans making from 33% to almost 100% of the total biomass flow of zooplankton. The greatest contribution came from the taxa reaching high values of biomass in particular months.

Fig. 5. The zooplankton biomass flow in [kg·day-1] at the sites studied in 2002 and 2003

Fig. 6. Relationship between the zooplankton biomass in [mg·L] and the biomass flow in [kg·day-1] at the sites studied in 2002 and 2003

Throughout the period of study, no statistically significant differences in the flow of biomass between the two sites were found (p<0.05). Relatively low values of standard deviation mean low differences in the biomass flow. A comparison of the time changes in biomass and biomass flow shows that the appropriate functions have similar character for both sites (Fig.6). The function for site 1 was described by the equation y = 57.918 * -2.0408, R2 = 0.9775, while for site 2 it was y = 37.347  * + 3.6068, R2 = 0.9151. The higher correlation coefficient for the samples collected at site 1 (0.95) than for those at site 2 (0.84) means that the function better approximates the actual measurements and that the scatter of the parameters analysed is smaller.

DISCUSSION

In the samples of zooplankton collected from the two retention reservoirs at the post-production waste-water treatment plant at the Chemical Plant Police, the dominant presence of rotifers was evident. At the outflow from the retention reservoir 1 (site ZbR 1) because of dense growth with macrophytes, the majority of individuals represented littoral and ubiquistic species. At the two sites the highest was the frequency of Copepoda larvae  and unidentified rotatoria. A characteristic feature of both sites was the continuous presence of the large D. magna and A. robustus in the summer months. These species were more frequently found at site 2, which is probably a consequence of the presence in reservoir 1 of large number of young fish (oral communication from the plant workers) feeding on the zooplankton, and the presence of fish may significantly affect the abundance of zooplankton [11,20,25,34]. The same opinion have Ejsmont-Karabin and Węgleńska [7], who reported that the large species of Cladocera preferred by fish were the first to disappear from the zooplankton represented at the outflow. Another reason for the differences between the two sites, mainly the lower abundance of zooplankton carrying out from reservoir 1 is the greater vegetation cover of this reservoir. Some authors have reported high abundances of zooplankton in littoral zones densely grown with macrophytes [4,14,33]. It is supposed that plankton crustaceans hide in the vegetation of the reservoir and do not get into the region of the current activity, hence are not carried out of the reservoir. This situation is related to diversification of the environmental conditions closely related according to Urabe [30], with zooplankton distribution. The water vegetation on the one hand provides the possible hiding places protecting against the attack of fish, but on the other hand it restricts the field of view [16,18]. According to Cerbin et al. [1], the water vegetation besides its positive role, slows down the development of zooplankton individuals, which leads to a decrease in zooplankton abundance. These authors report that in the absence of vegetation the individuals of D. magna faster reach maturity and grow to greater size. This observation seems to be confirmed by the results collected for reservoir 2, site site 2, which was not grown with submerged marcophytes and in which greater abundances of zooplankton were noted, in particular greater number of D. magna.

Szlauer [28] studied reservoir 1 in the late 1970s and early 1980s and reported the presence  of the same species occurring at the same proportions as found in this study at site 2. At the time of the Szlauer study [28] reservoir 1 was practically devoid of vegetation. For instance Szlauer noted D. magna and A. robustus only in summer months and zooplankton was practically absent in winter months. The presence of the above-mentioned species was noted by Czerniawski and Półgęsek [4] in June in the water of two sediment tanks at the Municipal Sewage Treatment Plant in Drawno (NW Poland). They reported a strong taxonomic domination of Cyclopoida in the first sediment tank devoid of vegetation, and the domination of Daphnia pulex and D. magna over Cyclopoida in the second tank grown in 100% with macrophytes. The water of the first tank practically did not contain small Rotifers possibly because of the presence of Copepoda predators, in particular A. robustus, E. serrulatus and Asplanchna sp., representing Rotifera. A similar situation was noted in the water flowing out from the retention reservoirs at the Chemical Plant in Police. In the months when the Cyclopoida representatives were present the number of taxa representing Rotatoria decreased. Also Devetter [6] indicated a great effect of the presence of crustacean predators on the qualitative and quantitative composition of the Rotifera. An interesting phenomenon is an abundant presence of D. magna in the retention reservoirs at the Chemical Plant in Police, especially at site 2. It is supposed that their abundant presence is related to the specific composition of the water in this reservoir, much different from those in lakes or rivers. The water containing significant amounts of phosphorus compounds despite preliminary treatment still contains the elements limiting the chemical composition and rate of primary production, which affects the development of plankton algae on which filtrating Cladocerans feed. It seems that such conditions are accepted by large Cladocerans, in particular by Daphnia sp., as indicated by their relatively high frequency and abundance in the second reservoir. This situation is not observed in the outflow from the first reservoir site 1, which can be a consequence of the presence of plants, according to Ejsmont-Karabin et al. [9] absorbing phosphorus regenerated by zooplankton. In this way the phytoplankton in the reservoir 1 gets poorer. The phytoplankton is the feed of filtrating Cladocerans and, according to George and Reynolds [10], there is a strong correlation between the biomass of phytoplankton and the quantitative structures of zooplankton. As reported by Kozłowska et al. [15] the less acidic the water the greater the fertility of the crustacean occurring in them and the water sent to the retention reservoirs in Police lose their acidity as a result of addition of calcium milk.

In the outflows from the retention reservoirs two quantitative peaks of zooplankton were noted in the year: the spring and the summer ones. Investigation of zooplankton carried out from eutrophic lakes also indicates the occurrence of such two peaks in a year [2,3,28]. The differences in the quantitative and qualitative composition of zooplankton at the two sites studied follow mainly from different abiotic and biotic conditions in these reservoirs. The purified post-production waste-water directed to the reservoirs seems not to have a negative effect on the development, frequency and abundance of zooplankton. According to Ejsmont-Karabin [8] who studied Rotifers in the polluted municipal reservoirs, many times the undesirable abiotic conditions in these reservoirs favoured the development of zooplankton and its high species diversity.

CONCLUSIONS

  1. Difference between two basins was not statistically significant, however differences in the composition of the zooplankton were visible.

  2. The presence or the lack of fish in the pond clearly influenced on the quantity and quality of zooplankton, particularly on big cladocerans – Daphnia magna.

  3. Quality of waters in basins didn't have probably negative influence on the zooplankton development.

  4. Zooplankton exported from basins can be used as the nutritional base for hatch and fry of fish.


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Accepted for print: 21.11.2008


Robert Czerniawski
Department of General Zoology, University of Szczecin, Szczecin, Poland
Z. Felczaka 3C
71-412 Szczecin
Poland
phone: +48 91 444 16 24
email: czerniawski@univ.szczecin.pl

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