Greener
Journal of Biological Sciences Vol. 11(2),
pp. 45-53, 2021 ISSN:
2276-7762 Copyright
©2021, the copyright of this article is retained by the author(s) |
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Planktonic Fauna
Distribution and Abundance in Relation to Physico-Chemical
Properties of Pindiga Lake, Gombe,
Nigeria.
1Umar, D. M.; 2Abbati,
M. A.
1Department of Biological Sciences, Gombe State University, Gombe,
Nigeria.
2Department of Biological Sciences, Federal
University of Kashere, Gombe,
Nigeria.
ARTICLE INFO |
ABSTRACT |
Article No.: 080721073 Type: Research |
Planktonic Fauna Distribution and
abundance in relation to Physico-chemical
properties of Pindiga Lake, Gombe
State were evaluated. Four sampling sites (A, B, C, and D) with distance of
500 meters apart were selected. Zooplankton samples were collected using
plankton net of 55µm mesh size by hauling horizontally for five meters. The
collected samples were preserved in 4% formalin and 3 drops of lugols iodine solution and transported to the Gombe State University, Biological Sciences laboratory
for counting and identification. Physico-chemical
properties were measured and planktonic fauna sampled fortnightly for a
period of six months (March-August, 2019). Planktonic fauna collected were
identified using taxonomic keys. Shannon Weiner diversity index was employed
for estimation of abundance and distribution. Results of the physico-chemical characteristics showed the ranges of
Air temperature, Water temperature, Water pH, Electrical Conductivity, Total
Dissolved Solid, Turbidity, Dissolved Oxygen, Biochemical Oxygen Demand,
Nitrate and Phosphate were 30.38-38.20C, 21.56-28.880C, 7.11-7.49,
264.5-321.25µS/cm, 132.25-160.75mg/L, 16.88-22.75mg/L, 3.6-5.74mg/L,
1.89-3.18mg/L, 8.79-10.98mg/L and 2.49-3.89 mg/L respectively. The
planktonic fauna results revealed a total of 1542 individual species of
zooplankton in 28 genera among the three zooplankton taxa of Cladocera, Copepoda and Rotifera. The genera abundance of Pindiga
Lake arranged in dwindling trend as Copepoda>Rotifera> Cladocera, with
respective total zooplankton values of 44.94%, 32.23%, and 22.82%. Copepod, Cladocera and Rotifera were
negatively interrelated to Air temperature, Water temperature, Electrical
conductivity, Total dissolved solid, nitrate and phosphate while positively
concurrent to Dissolved Oxygen and Biochemical Oxygen Demand. Outcome of the
investigation point out that physicochemical properties were within the
range value recommended for most tropical water bodies and profusion of
zooplankton is exceedingly elating compare to other water bodies.
Subsequently, the lake is suitable to sustain the proliferation,
continued existence and development of aquatic organisms predominantly fish.
The research showed that there is abundance of zooplankton, which will serve
as a food to fish, hence there is need to stock a fish into the water body
in order to maintain the stability of the ecosystem. |
Accepted: 07/08/2021 Published: 31/08/2021 |
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*Corresponding Author Abbati
MA E-mail: danladiumar97@
gmail.com |
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Keywords: |
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INTRODUCTION
Water is the most crucial assets and general solvent that
all living creatures depend on for their existence, growth and reproduction
(Samuel, et al., 2015). Without water
living organisms are expected not to survived, growth and reproduced since it’s
the portion of life. Good water quality is requisite in conserving the
composition of aquatic flora and fauna, deterioration of the water quality can
cause turn down in productivity and biodiversity of aquatic biota (Faithful and
Finlayson, 2005). The quality of water is ascertained by its physical and
chemical properties. Due to intensifying population growth and anthropogenic
processes, water quality is dwindling each day (Alrumman
et al., 2016). Decline of lentic
water quality has been linked to both biogenic and anthropogenic activities,
including volcanic eruptions, earthquake, climate change, precipitation,
agricultural land use and sewage discharge.
Water necessities in all living organisms are
intensifying day after day, but the source of water for drinking is a decisive
issue, as all water supplies have got to the point of predicament due to
urbanization and industrial revolution (Bibbi et al., 2016). Pollution of water
occurred when there is alteration in the physical, chemical or biological
condition in the ecosystem which disastrously affects the treasure of human
life together with other fauna and flora (Ojitiku et al., 2018). The density and diversity
of the planktons are greatly influenced by the different physicochemical
parameters of water (Krishna et al.,
2014). Zooplanktons are minute drifting and suspended organisms floating at the
surface of the water body, which are essential components of water food web, as
they have a say to the productivity of freshwater ecosystems. They are also
very prone to changing ecosystem; therefore, they compose perfect indicator
organisms. Zooplanktons are the important aquatic organisms occurring profusely
in all sorts of aquatic habitats, and they play a crucial role in energy
transfer of aquatic ecosystem (Siddique and Kale, 2018). The aimed of the
research is to investigate the zooplankton as a fish feed and physicochemical
properties as a condition for fish growth, survival and reproduction in Pindiga lake.
Pindiga Lake
is an artificial and perennial small water body that receives its water
directly from rain. It’s located in the eastern part of Pindiga
about 1km to Pindiga Village in Akko Local Government
Area of Gombe State. The lake lies between latitude
10.13°15N and longitude 11.11°19E (Fig. 1). It has the surface area of 513m by
502m. The activities carried out around the water body include washing,
bathing, livestock consumption and car washing.
Figure 1: Map of Gombe State Showing
Location of Study Area and Sampling Stations
Source: GIS Unit, Department of
Geography, Gombe State University
Zooplankton abundance and distribution of Pindiga Lake, Gombe State were
evaluated. Four sampling stations (A, B, C, and D) with distance of 500 meters
apart were selected and
replicated samples were collected at each point throughout the study period.
Water samples were collected from four different locations on the lake and mean
values of the four stations were worked out and recorded. The sampling was
conducted fortnightly between March to August,
2019. Sampling was done between 8.00am
and 10.00am.
Temperature (°C) of the air was determined in situ by
exposing a bulb mercury in glass thermometer in the
air at each sampling station for about 1-2 minutes and the readings were
recorded in degree Celsius (APHA, 2005). Water temperature was determined in
situ by dipping mercury in glass thermometer into the water at each station for
about 1-2 minutes and readings were recorded (APHA, 2005). pH was measured using Hanna pH meter (Model H199107), the
tip of the pH meter was immersed into the 100ml beaker containing water sample
for 2-3 minutes and readings were recorded (APHA,
2005). Electrical conductivity was measured with Hanna conductivity meter
(Model EC 215), the Water samples was drawn in a wide mouthed beaker and the
tip of the conductivity meter was dipped into a beaker for a period of 2-3
minute to permit constant reading (APHA, 2005).Total Dissolved Solid was
determined with Hanna TDS meter microprocessor (Model H215), the water samples
were drawn in a 100ml beaker and the tip of the TDS meter was dipped into a
beaker for a period of 2-3 minute to permit constant reading (APHA, 2005).Turbidity was measured with black-white secchi disc. Turbidity was measured by gradually lowering
the Secchi disc at respective sampling points. The
depth at which it disappears in the water (X1) and reappears (X2) was noted and
estimated as the average of points of disappearance and reappearance (APHA,
2005). Hanna Dissolved Oxygen
microprocessor (Model HI 98186) was used to measure the dissolved oxygen. Sample of the water was collected in 100ml
beaker; the electrode of dissolved oxygen microprocessor was dipped into the
beaker that contains the sample water for about 2-3 minutes. The reading was
recorded in mg/l (APHA, 2005). Hanna
Dissolved Oxygen microprocessor (Model HI 98186) was used to determine the
biochemical oxygen demand, 100ml part of the sample collected was incubated for
five days in dark cupboard at room temperature and dissolved oxygen was
determined after five days of incubation, the difference between the initial
value of dissolved oxygen and the value after five days of incubation was used
as value of biochemical oxygen demand in the water sample (APHA, 2005. The Palintest multiparameter (Model
7100) colorimeter was used to determine the nitrate using the nitra ver. 5 nitrate reactivo reagent. The reagent was added to the sample
collected in a 20ml colorimeter vial and placed in a colorimeter compartment
and then closed with the colorimeter cover and allowed for a period of time
sufficient to permit constant reading. The value obtained was recorded in mgl-1(APHA,
2005). The Palintest multiparameter
(Model 7100) colorimeter was used to determine the phosphate using the
Armstrong reagent. The reagent was added to the sample collected in a 20ml
colorimeter vial and placed in a colorimeter compartment and then closed with
the colorimeter cover and allowed for a period of time sufficient to permit
constant reading. The value obtained was recorded in mgl-1(APHA,
2005).
Zooplankton sampling, counting and Identification
Zooplankton samples were collected using plankton net of
55µm mesh size by hauling horizontally for five meters. The collected samples
were preserved in 4% formalin and 3 drops of lugols
iodine solution and transported to the Gombe State
University, Biological Sciences laboratory for counting and identification (Saidu et al., 2016
and Isah et
al., 2018).
The resultant concentrated
zooplankton sample was transferred into plastic container and preserved with 4%
formalin and 3 drop of lugol’s iodine solution
according to the method used by Isah et al., (2018). The samples were labelled with the date, time of
sampling, study area-lake name, sampling site name and the volume measured and
pasted on the containers (Umar, 2014).
All collected samples were transported in a cool box containing ice to
the laboratory for analysis. In the
laboratory the 20ml out of 100ml in each sample collected was filtered using
the Whitman’s filter paper and the 1ml of the resultant concentrate was
collected for identification and counting. 1ml of filtered sample was spread on
to a slide and counted the individual present in number per ml. Zooplankton
counts were made by shaking each sample to share out organisms uniformly and
one drop was put on top of a clean glass slide by the use of pipette. This was
then watchfully covered with a cover slip and brought under Olympus binocular
microscope at 400× and 1000× magnification for further taxonomic analysis. The
zooplankton was identified using applicable standard zooplankton keys like
Graham (2007), Witty (2004), Petersen, (2018) and Phan et al., (2015). The Zooplankton distribution and abundance were
analyzed and presented using Excel Microsoft and Minitab software. Shannon Weiner diversity
index was employed to estimate the monthly abundance of zooplankton.
One-way Analysis of variance was
used to test the significant differences in mean of physico-chemical
properties among months and Fisher Least Significance Difference (FLSD) was
used to separate the means of significant differences where exist. Correlation
was employed to test the relationship between the physicochemical properties
and zooplankton abundance and distribution at P<0.05 level of significance
using Minitab19.2020 software.
RESULT AND DISCUSSION
The results
of the physicochemical properties were presented in table 1. The ranges of
Water temperature (21.6-28.90C) recorded in Pindiga
lake was slightly lower than the
ranges reported by Abubakar et al., (2015) conducted in Dadin Kowa reservoir, Gombe State, Saidu et al.,
(2016) conducted in Balanga dam, Dimowo,
(2013) conducted in river Ogun, Abeokuta, Ogun State and higher than the range
reported by Usman and Yerima,
(2017) in Ajiwa reservoir, Katsina
State. The difference was might be due to differences in location, altitude and
other factors such as cloud cover, vegetation and level of penetration of
sunlight.
Water pH ranges between (7.11-7.49), The
pH ranges recorded during the study period was higher than the ranges reported
by Otene et
al., (2019) in a research conducted at Okamini
Stream, Port Harcourt and lower than the ranges reported by Abubakar
et al., (2015) conducted in Dadin kowa, Usman
and Yerima, (2017) conducted in Ajiwa
river, Katsina State. Dimowo,
(2013) conducted a field research in River Ogun, Abeokuta, Ogun
State, Ekpo, (2013) conducted in tropical rain forest
river in Niger Delta, Nigeria, Azuka et al., (2018) conducted at Ikpoba river. The differences might be due to the amount of
decomposition and inflow of inorganic nutrient into the water bodies.
Electrical Conductivity (264.5-321.3µm/S) Electrical conductivity had
its highest mean value during the month of April and lowest mean value during
the month of July agreed with the findings of Usman
and Yerima, (2017) in a field research conducted in Ajiwa river, Katsina State, who
reported the highest electrical conductivity during the month of April and
lowest value recorded during the month of August. The low value of Electrical
conductivity in July might be due to low concentration of ions due to dilution
effect of rainfall and highest in April was due to high concentration of ions
in the water body. The range mean value of
conductivity in Pindiga Lake was higher than the
electrical conductivity range reported by Abubakar et al.,
(2015) conducted in Dadin Kowa
reservoir, Gombe State, Esenowo
et al., (2017) conducted in Nwaniba, River state, Isah et al., (2018) conducted in Dadin kowa Dam, Gombe State and lower than the range reported by Usman et al., (2019) conducted in Kashimbila river, Takum, Taraba State. The differences might be to the level of
inflow of ions into the water body and variation caused by the topography.
Total Dissolved Solid (132.25-160.8mg/L) Total dissolved solid had its
highest mean value of during the month of April and lowest mean value of during
the month of July agreed with the findings of Usman
and Yerima, (2017) in a field research conducted in Ajiwa river, Katsina State, who
reported the highest Total dissolved solid during the month of April and lowest
value recorded during the month of August. The low value of Total dissolved
solid in July might be due to low solubility of solid and low inflow of water
into the system and highest in April was due to low water in the lake which may
increase the concentration of solute in the water body.
The range mean value of Total dissolved solid in Pindiga Lake was higher than the Total dissolved solid
range reported by Abubakar et al., (2015) conducted
in Dadin Kowa reservoir, Gombe State, Esenowo et al., (2017) conducted in Nwaniba, River state, Isah et al., (2018) conducted in Dadin kowa Dam, Gombe State and lower than the range reported by Usman et al., (2019) conducted in Kashimbila river, Takum, Taraba State. The differences might be to the nature of the
water body and variation caused by the topography. Total dissolved solids which
mostly consist of organic and inorganic substances dissolved and washed into
the lakes by runoffs are very essentials in the survival, growth and
reproduction of aquatic organisms (Umar, 2014).
Table 1: Mean±SEM of physico-chemical properties throughout the study period
(March-August, 2019) in Pindiga Lake, Gombe, Nigeria.
|
|
|
Months |
|
|
|
|
Physicochemical |
March |
April |
May |
June |
July |
August |
Range |
Air temp. (0C) |
38.2±0.8a |
36.6±0.6b |
36.75±0.3b |
32.74±0.2c |
30.4±1.03d |
32.1±0.75c |
30.4-38.2 |
Water temp. (0C) |
28.9±1.01a |
25.6±0.28b |
26.5±0.48b |
23.3±0.26c |
21.6±0.52d |
22.1±0.88d |
21.6-28.9 |
pH |
7.1±0.35a |
7.3±0.11a |
7.5±0.17ab |
7.4±0.05abc |
7.2±0.17bcd |
7.5±0.03cd |
7.1-7.49 |
E.C(µS/cm) |
301.5±16.2a |
321.3±2.5b |
318±5.2b |
278.3±1.5c |
264.5±2.7c |
292.8±2.5d |
264.5-321.3 |
TDS (mg/L) |
151±8.3a |
160.75±1.2b |
159±2.6b |
139.1±0.75c |
132.3±1.3c |
146.38±1.3a |
132.3-160.8 |
Turbidity (cm) |
22.8±1.19a |
20.3±2.4b |
16.9±2.39c |
18.8±0.65bc |
19.9±1.3 |
20.9±0.75abd |
16.9-22.8 |
DO (mg/L) |
3.6±1.03c |
3.98±0.36bc |
4.3±0.12b |
5.07±0.12a |
5.53±0.1a |
5.74±0.19a |
3.6-5.74 |
BOD (mg/L) |
1.99±0.65bc |
1.9±0.29bc |
2.07±0.06b |
2.24±0.09b |
3.18±0.13a |
2.96±0.1a |
1.9-3.18 |
Nitrate (mg/L) |
9.22±2.12bc |
10.66±1.2ab |
10.98±0.3a |
9.91±0.41abc |
8.79±0.21c |
10.94±0.14a |
8.79-10.98 |
Phosphate (mg/L) |
2.49±0.32d |
3.05±0.15b |
2.93±0.17bc |
2.73±0.17cd |
2.8±0.09bc |
3.89±0.17a |
2.49-3.89 |
Mean
value with same superscripts are not significant difference (p≤0.05), Key: pH= Percentage of hydrogen, E.C= Electrical Conductivity,
D. O=Dissolved Oxygen; BOD=
Biochemical Oxygen Demand
Turbidity (16.9-22.8cm) Turbidity had its highest mean
value during the month of March and lowest mean value of during the month of
July and May contrary to the findings of Usman and Yerima, (2017) in a field research conducted in Ajiwa river, Katsina State, who
reported the highest Turbidity during the month of August and lowest value
recorded during the month of May. The low value of Turbidity in July and May
might be due to high transparency and low turbulences of water caused by
excessive usage of the inhabitant and highest in April was due to high water
usage in the lake which may increase the turbulence and upset the water body. The range mean value of Turbidity in Pindiga
Lake was similar to the range reported by Abubakar et al.,
(2015) conducted in Dadin Kowa
reservoir, Gombe State, Esenowo
et al., (2017) conducted in Nwaniba, River state, Isah et al., (2018) conducted in Dadin kowa Dam, Gombe State and lower than the range reported by Usman et al., (2019) conducted in Kashimbila river, Takum, Taraba State.
Dissolved Oxygen (3.6-5.8mg/L) The
Dissolved oxygen range recorded during the study period was similar to the
ranges reported by Otene et al., (2019) in a research conducted at Okamini
Stream, Port Harcourt, Abubakar et al.,
(2015) conducted in Dadin kowa,
Isah et al., (2018) at Dadin
kowa Reservoir and slightly lower than the ranges
reported by Usman and Yerima,
(2017) conducted in Ajiwa river, Katsina
State, Dimowo,
(2013) conducted a field research in River Ogun, Abeokuta, Ogun
State, Imaobong, (2013) conducted in tropical rain
forest river in Niger Delta, Nigeria, Azuka et al., (2018) conducted at Ikpoba river.
The
differences might be due to differences in temperature and solubility of gases.
Therefore, the dissolved oxygen of Pindiga Lake is within the required range of good water
quality. The highest dissolved oxygen was recorded during the month of August
which agreed with the finding of Usman and Yerima, (2017) reported in a field research conducted at Ajiwa river, Katsina
State and Similar to the findings of Abubakar et al., (2015). High dissolved oxygen
observed during the month of August was caused as a result of low temperature
and high solubility of gases. Dissolved oxygen is an essential factor that facilitates
the survival, growth and reproduction of aquatic organisms. The dissolved
oxygen concentrations ranged 3.6mg/l to 5.7mg/l and hence, the concentrations
were within the required range. The amount of dissolved oxygen in water has
been reported not static but dynamics, depending on temperature, depth, wind
and extent of living organisms such as decomposition (Indabawa,
2009). Low dissolved oxygen affects the growth of many organisms and enhances
the rate of metabolic activities (Charles, 2003); therefore, adequate dissolved
oxygen is essential for all living organisms. The lower the dissolved oxygen
the poorer will be the water quality (Umar, 2014).
Biochemical Oxygen Demand (1.9-3.2mg/L), Biochemical oxygen
demand range recorded during the study period was similar to the ranges
reported by Abubakar et al., (2015) conducted in Dadin kowa reservoir, Gombe State, Isah et al., (2018) at Dadin
kowa Reservoir, Gombe
State, Otene et
al., (2019) in a research conducted at Okamini
Stream, Port Harcourt and slightly lower than the ranges reported by Dimowo, (2013) conducted a field research in River Ogun,
Abeokuta, Ogun State; Imaobong,
(2013) conducted in tropical rain forest river in Niger Delta, Nigeria; Usman and Yerima, (2017)
conducted in Ajiwa river, Katsina
State, Azuka et al., (2018) conducted at Ikpoba river.
Phosphate ranged between (2.5-3.9mg/L), the range mean value of phosphate value in Pindiga Lake was higher than the phosphate range reported
by Abubakar et
al., (2015) conducted in Dadin Kowa reservoir, Gombe State, Esenowo et al., (2017) conducted in Nwaniba, River state, Isah et al., (2018) conducted in Dadin kowa Dam, Gombe State and lower than the range reported by Usman et al., (2019) conducted in Kashimbila river, Takum, Taraba State. The variation might be due to the nature of
the water body as a close system and variation caused by the topography. Phosphorus plays an important role in the determination
of the productivity of an ecosystem, which in turn can affect the number of
trophic level in a food web and its stability. The presence of nutrients and
plant biomass formation in water body exhibit a complex dynamic relationship in
tropical aquatic ecosystem due to various physico-chemical
and biological characteristic (Siddique and Kale,2018).
Nitrate ranges between (8.8-10.1mg/L), the range mean value of Nitrate in Pindiga
Lake was higher than the range of Nitrate reported by Esenowo
et al., (2017) conducted in Nwaniba, River state, Abubakar et al.,
(2015) conducted in Dadin Kowa
reservoir, Gombe State, Isah
et al., (2018) conducted in Dadin kowa Dam, Gombe State and lower than the range reported by Usman et al., (2019) conducted in Kashimbila river, Takum, Taraba State.
Result of zooplankton in Pindiga
lake is contrary to the research conducted by Usman and Yerima, (2017) who
reported four different taxa of zooplankton in Ajiwa
river, Katsina State and agreed with the finding of
Emmanuel et al., (2008) who reported
three taxa of Zooplankton in Calabar river. The
Copepods were the most abundant zooplankton taxon of the zooplankton abundance.
Likewise, results have been reported by Erondu and
Solomon (2017) in Behind Girls hostel, University of Abuja and Emmanuel et al., (2008) in Calaba
river, Nigeria. Their abundance was may be due to
their acclimatization to altering ecological condition and capability to bear
up varying ecological hassle (Emmanuel et
al., 2008). The abundant of Copepoda is also
dependent on availability of sufficient nutrients and favorable temperature
(Sharma et al., 2013).
The second most abundant taxon was Cladocera
of the total zooplankton abundance this finding is in disagreement with the
findings of Abba et al., (2016) who
stated that cladoceran were least zooplankton species
in Kpata lake, Lokoja, Nigeria. Their abundance would be attributed to
their capability to undergo upright movement, which lessens competition through
niche exploitation and food utilization (Usman and Yerima, 2017). Cladocera have
widely been used as biological indicators in studies due to their sensitivity
to various levels of water quality characteristics (Radix, et al., 2002).
Rotifera is
the least abundant zooplankton in the study area similar to the statement of Forro (2010) who reported that Rotifera
are the least abundant zooplankton in freshwater and contrary to the finding of
Abba et al., (2016) who reported that
rotifer is the second most abundant zooplankton in Kpata
Lake, Lokoja, Nigeria. The result also shows that copepod
has a total number of 13 genera contrary to the report of Ekpo, (2013) in a field research conducted
in a tropical rain forest river in Niger Delta, Nigeria, who reported the number of species fall under
copepod as 9 species Cladocera
consisting of 7 genera and Rotifera comprises 8
genera of species richness, consequently, Copepoda is
the richest of all zooplankton taxa followed by Rotifera
then Cladocera.
The percentage of copepods in Pindiga
lake was closely similar to the finding of Solomon and Erondo,
(2018) who reported almost the same percentage of copepods in a field
research conducted at behind girl’s hostel, university of Abuja on
Identification of planktons (zooplankton and phytoplankton), contrary to the
finding of Usman and Yerima,
(2017) who reported lower percentage of copepods in a field research conducted
on ecological investigation of zooplankton abundance in Ajiwa
reservoir, Katsina State, Nigeria, as the most least
abundance zooplankton taxon in the water body. The variation may be as result
of anthropogenic activities carried out around the water body.
Table 2: Monthly zooplankton abundance and
distribution in Pindiga Lake, Gombe
State, Nigeria
|
|
|
Months |
|
|
|
Taxa |
March |
April |
May |
June |
July |
August |
Copepoda |
47.32 |
47.78 |
46.89 |
43.87 |
41.36 |
45.29 |
Skistodiaphthamus sp. |
6.25 |
4.93 |
6.7 |
5.2 |
4.94 |
5.86 |
Leptodiaphthamus sp. |
5.36 |
0.99 |
5.74 |
4.46 |
3.7 |
4.93 |
Macrocyclops sp. |
6.25 |
7.39 |
4.31 |
5.2 |
4.32 |
3.76 |
Paracyclops sp. |
2.68 |
8.37 |
5.26 |
2.97 |
3.4 |
5.63 |
Senecella sp. |
2.68 |
4.93 |
7.66 |
6.69 |
4.94 |
5.16 |
Acanthocyclops sp |
1.79 |
2.96 |
2.87 |
2.23 |
1.85 |
5.16 |
Limnocalanus sp. |
4.46 |
0 |
0.96 |
1.12 |
0.62 |
3.29 |
Tropocyclops sp. |
8.93 |
8.37 |
3.35 |
1.86 |
2.16 |
3.05 |
Nauplius sp |
0 |
0 |
1.44 |
8.92 |
8.64 |
3.29 |
Cathocamptus sp. |
0 |
3.94 |
2.87 |
2.23 |
1.85 |
3.05 |
Diacyclops sp. |
4.46 |
3.94 |
3.82 |
2.97 |
4.94 |
2.11 |
Aglaodiaphthamus sp. |
4.46 |
0.99 |
1.91 |
0 |
0 |
0 |
Mesocyclops sp. |
0 |
0.99 |
0 |
0 |
0 |
0 |
Cladocera |
24.11 |
22.66 |
22.01 |
36.43 |
34.26 |
39.67 |
Bosmina sp. |
4.46 |
2.46 |
3.35 |
6.69 |
4.63 |
8.22 |
Diaphanosoma sp. |
0 |
0 |
0 |
3.72 |
7.41 |
0 |
Eubosmina sp. |
0 |
0 |
0 |
4.46 |
0 |
7.04 |
Daphnia sp. |
8.04 |
2.46 |
3.35 |
7.43 |
4.94 |
5.63 |
Ceriodaphnia sp. |
0 |
1.97 |
2.39 |
4.83 |
4.01 |
5.63 |
Macrothrix sp |
6.25 |
8.87 |
2.87 |
4.46 |
5.86 |
5.4 |
Moina sp. |
5.36 |
6.89 |
10.05 |
4.83 |
7.41 |
7.75 |
Rotifera |
28.57 |
29.56 |
31.1 |
19.7 |
24.38 |
15.02 |
Asplanchna sp. |
4.46 |
4.43 |
8.13 |
2.23 |
3.4 |
2.58 |
Brachianus sp. |
2.68 |
9.36 |
2.87 |
5.95 |
6.79 |
2.82 |
Keratella sp. |
6.25 |
3.45 |
7.66 |
1.49 |
2.47 |
2.82 |
Polyarthra sp. |
8.96 |
7.88 |
4.31 |
2.6 |
5.56 |
3.52 |
Trichocerca sp. |
0 |
0.99 |
3.35 |
1.12 |
6.17 |
0.47 |
Synchaeta sp. |
2.68 |
2.96 |
4.78 |
6.32 |
0 |
2.82 |
Hexarthra sp. |
0 |
0.49 |
0 |
0 |
0 |
0 |
Anuraepsis sp. |
3.57 |
0 |
0 |
0 |
0 |
0 |
Shannon index(H) |
3.44 |
4.26 |
4.74 |
5.57 |
5.87 |
6.86 |
Evenness (E) |
1.15 |
1.38 |
1.50 |
1.75 |
1.89 |
2.19 |
Results showed that there was
significant correlation between zooplankton abundance and some physico-chemical properties this is in agreement with the
findings of Ewa et
al., (2017) who also reported significant correlation between the
occurrence of zooplanktons and some physicochemical characteristics in coastal
Vistula lagoon. Suresh et al., (2011)
also reported that different
environmental factors, affecting the characteristics of water have enormous
impact upon the growth and abundance of zooplankton. Increase in temperature in
Pindiga lake decrease the abundance of zooplankton
while increase in the amount of dissolved oxygen in the lake increases the
abundance of zooplankton as agreed to the findings of Usman et al, (2019) who reported that increase
in temperature significantly reduces the zooplankton abundance while increase
in dissolved oxygen increase the abundance of zooplankton in a field research
conducted at Kashimbila river, Takum,
Taraba state on Survey of Zooplankton Diversity and
Abundance and Its Relationship with Physicochemical Parameters in River Kashimbila Takum, Taraba State, Nigeria. Usman and Yerima, (2017) also reported in a field research conducted
on ecological investigation of zooplankton abundance in Ajiwa
reservoir, Katsina State, Nigeria, that increase in
Dissolved oxygen lead to the increase in abundance of zooplankton as
investigated, likewise the report suggested by Ekpo,
(2013) that increase in temperature mostly decrease the number of species
present in a tropical rain forest river in Niger Delta, Nigeria, similarly
reported by Solomon and Erondo, (2018) in a field
research conducted at behind girl’s hostel, university of Abuja on
Identification of planktons (zooplankton and phytoplankton), that the abundance
of zooplankton increased with the increase in dissolved oxygen and decrease
significantly with increases in temperature.
Table 3: Correlation matrix showing
relationship between Zooplankton taxa and Physico-chemical
characteristics in Pindiga Lake, 2019.
Properties |
Air temp |
temp |
pH |
E.C |
TDS |
Turbi. |
DO |
BOD |
Nitrate |
Phos |
Cop |
Clado |
Rotif |
Water temp |
0.973 |
||||||||||||
Water pH |
-0.11 |
-0.28 |
|||||||||||
E.C |
0.837 |
0.692 |
0.323 |
||||||||||
TDS |
0.841 |
0.697 |
0.316 |
1 |
|||||||||
Turbidity |
0.138 |
0.212 |
-0.619 |
-0.109 |
-0.101 |
||||||||
DO |
-0.954 |
-0.956 |
0.337 |
-0.713 |
-0.718 |
-0.191 |
|||||||
BOD |
-0.891 |
-0.838 |
-0.017 |
-0.758 |
-0.76 |
0.066 |
0.895 |
||||||
Nitrate |
0.249 |
0.044 |
0.897 |
0.684 |
0.678 |
-0.423 |
-0.016 |
-0.289 |
|||||
Phosphate |
-0.366 |
-0.517 |
0.676 |
0.098 |
0.094 |
-0.009 |
0.573 |
0.451 |
0.656 |
||||
Copepod |
-0.787 |
-0.868 |
0.553 |
-0.4 |
-0.405 |
-0.129 |
0.913 |
0.775 |
0.32 |
0.855 |
|||
Cladocera |
-0.854 |
-0.884 |
0.395 |
-0.587 |
-0.591 |
0.01 |
0.95 |
0.838 |
0.115 |
0.742 |
0.966 |
||
Rotifera |
-0.689 |
-0.758 |
0.311 |
-0.305 |
-0.311 |
-0.538 |
0.677 |
0.654 |
0.118 |
0.412 |
0.63 |
0.514 |
1 |
Bold font indicated that
correlation is significant at (p<0.05)
The result of zooplankton
throughout the months revealed that all the months were highly rich in the
assemblage of zooplankton with almost all representatives of species. This
could be as a result of favorable environmental conditions. This agreed with Alexander,
(2012) who suggested that the abundance of zooplankton depends on a number of
factors such as climatic change, habitat physico-chemical
characteristics and biotic factors.
Abubakar,
U.M., Umar, D.M. and Zainab, M.Z. (2015). Effects
of Physicochemical parameters on Oreochromis Niloticus in Dadin Kowa Reservoir, Gombe State,
Nigeria, International Journal of
Advances in Chemical Engineering and Biological Sciences 2(2): 110-112.
Akpomie, O.O., Buzugbe, H.S. and Eze, P.M. (2014). Effects of Brewery Effluents on the
Microbiological Quality of Ikpoba River and
Surroundings Borehole Water in Benin-City, Nigeria. British Microbiology Research Journal, 5(1): 76-82.
Alexander, R. (2012). Interaction
of zooplankton with cyanobacterias, Msc. Dissertation, University of Nebraska,
p69.
Alrumman, S. A., El-kott, and A.F., Kehsk M.A. (2016). Water pollution: Source and treatment. American Journal of
Environmental Engineering.
6(3):88-98.
American
Public Health Association (2005). Standard
methods for examination of water and wastewater,
21st edition. American publication Health Association,
Washington, DC. p1121
APHA (2005):
Standard method for the examination of
water and waste water", American Public Health Association, Washington
D.C. p1089.
Azuka, R. A., Imah, J.F., Grace, I.
A. and Helen, O. (2018). Seasonal
variation in the physicochemical parameters of Ikpoba
river water samples, International
Journal of Life Science and Scientific Research 4(3):1810-1821.
Bibi, S., Khan, R. L., Nazir,
R., (2016) Heavy metals in drinking water of LakkiMarwat
District, KPK, Pakistan. World Applied Sciences Journal, 34(1):15-19.
Emmanuel, C.
U., Chinasa, U., Akpan,
P.A., Ekpeme, E. M., Ogbeche,
L. U. and Asor, J. (2008). Bio-survey of plankton as indicators
of water quality for recreational activities in Calaba
River, Nigeria. Journal of Applied
Sciences and Environmental Management, 12(2):35-42.
Erondu, C.J. and Solomon, R. J. (2017): Identification of
plankton (zooplankton and phytoplankton) behind Girls Hostel University of
Abuja, Nigeria. Direct Research Journal
of Public Health and Environmental Technology. 2(3):21-29.
Esenowo, I.K. and Ugwunba, A.A.A.
(2010), Composition and abundance of Macro benthos in Majidun
River Ikorodu Lagos State, Niger, Research Journal of Biological Sciences,
5(8):556-560.
Ewa, P., Agnieszka, G., Jacek, K.
and Magdelenan, B. (2017). Effect of Physicochemical Parameters on Zooplankton in
The Brackish, Coastal Vistula Lagoon, oceanologia, 59(1):49-56.
Faithful,
J., and Finlayson, W. (2005). Water quality assessment for sustainable agriculture in the Wet
Tropics—A community-assisted approach. Marine Pollution Bulletin. 31; 51(1):99-112.
Forro, l., Korovchinsky, N.M., Kotov, A.A., Petrusek, A. (2008). Global Diversity of Cladoceran (Cladocera;
Crustacean) in Fresh Water Animal Diversity Assessment. Hydrobiologia,
595: 177 – 184.
Graham, F. (2007): Quick guide to free-living
orders of New Zealand freshwater Copepoda,
Terrestrial and Freshwater Biodiversity Information System, Taihoro
Nukurangi, 10.
Saidu,
H., Usman, B and Umar, D. M. (2016) Studies of Species Distribution for
Phytoplankton in Balanga Dam. Journal of Advanced Research in Applied
Sciences and Engineering Technology 3(1):1-9.
Imaobong, Ekpo(2013) Effect of
physicochemical parameters on zooplankton species and density of a tropical
rain forest river in Niger Delta, Nigeria. International
Journal of Engineering and Science 2:13-21
Indabawa, I.I. (2009). Studies on Limnological Parameters and Phytoplankton Dynamics of Nguru Lake, Yobe State, Nigeria.
Bioscience Research Communications,
21(4):183-188.
Isah, Z., Abubakar, K. A, Umar,
D.M. and Hassan, S.K. (2018): A Study On Phytoplanktonic Composition in Dadin
Kowa Dam, Gombe State,
Nigeria. Greener journal of biological
sciences 8(2): 45-50.
Krishna,
P.V., Madhusudhana, R., Jyothirmayi,
V., and Hemanth, K.V. (2014) Biodiversity of
Zooplankton communities in a perennial Pond at Lake Kolleru
Region of Andha Pradesh, India. International
Journal of Advanced Research 2(7): 33-41.
Ojitiku, R.O., Habibu, S. and Kolo, R.J. (2017). Zooplankton abundance and diversity of
River Kaduna and college of Agriculture and animal science dam (CAAS) Kaduna,
Nigeria. Nigerian Journal of Fisheries
and Aquaculture, 5(2):1-10.
Otene, B.B., Alfred-Okiya, J.F. and Amadi, F. (2019) Physicochemical properties and zooplankton community
structure of Okamini stream, Port Harcourt, Nigeria. International Journal of Research and
Innovation in applied Science, 4: 100-107.
Peterson, F. (2018). An illustrated Key to the Philippine Freshwater Zooplankton.
Including some brackish water species from Laguna de Bay.
p460.
Phan, D. D.,
Nguyen, V.K., Le, T. N. N., Dang, N.T. and Ho, T.H. (2015). Identification Handbook of Freshwater Zooplankton of the
Mekong River and its tributaries, Mekong River Commission, Vientiane. p207.
Pieri,
V., Martens, K., Rossetti, G. (2009). Distribution
and ecology of non-marine ostracods (crustacean, ostracods) from Friuli Venzia
Giulia (NE Italy). Journal of
limnology, 68(1):10-15.
Radix, P., Serverin,
G., Schramm, K.W. and Kettrup, A. (2002).
Reproduction disturbances of Brachianus calyciflorus(rotifer)
for the screening of environmental endocrine disrupters, Journal of Chemosphere, 10:1097-1101.
Saidu,
H., Usman, B. and Umar, D. M. (2016): Studies of Species Distribution for
Phytoplankton in Balanga Dam, Journal of Advanced Research in Applied Sciences and Engineering
Technology, 3(1): 2462-1943.
Shiel, R. J. (1995). A guide to Identification of rotifers, copepods and clacedorans from Australia inland Waters.
Cooperative research Centre for fresh waters ecology. Identification guide 3:
p144.
Siddique, K.F. and Kale, M. K. (2018):
Species diversity of zooplankton and physicochemical parameters of Bindusara Dam from Beed district
Maharashtra, India, International Journal
of universal print, 4(6):308-319.
Uduma, A.U. (2014). physicochemical
analysis of the quality of sachet water consumed in kano
metropolis. American Journal of
Environment, Energy and Power Research, 2: 1-10.
Umar, D. M.
(2018). Practical Hydrobiology Manual for Fisheries
Scientists, Department of Biological Sciences, Gombe
State University, Unpublished. p36.
Umar, D. M.,
Harding, J. S. and Chapman, H. M. (2014). Tropical land use and its effect on
stream communities. Journal of Environmental and Policy Evaluation. 4(2),
165-195.
Umar, M. A., Abubakar,
K.A., Ali, J. (2017). Aquacultural attributes of some
water physicochemical parameters: a review, Scholars
Academic Journal of Biosciences. 5(6):440-445.
Usman. L. U and Yerima, R. (2017).
Ecological investigation of zooplanktons abundance in Ajiwa
reservoir Katsina State-Nigeria, International Journal of Applied Biological Research, 8(1):50-69.
Witty, L.M.
(2004). Practical guide to
identifying freshwater crustacean zooplankton. 2nd edition
Sudbury, Ontoria: Cooperative Freshwater Ecology
Unit. p60.
Cite this Article: Umar, DM; Abbati,
MA (2021). Planktonic Fauna Distribution and Abundance in Relation to Physico-Chemical Properties of Pindiga
Lake, Gombe, Nigeria. Greener Journal of Biological
Sciences, 11(2): 45-53. |