5
C Effect of Waste Sew Fr Hab Department of Z Abstract – Effect of sewage pollutio diversity of fresh water ecosystem of west India was carried out between February 2010, by investigating the biological en habitats. The faunal species were obtain sediment with 0.5mm mesh sieve and phys of ten major taxonomic groupings wer groupings and their percentage contrib macro-benthic organisms collection ar Diptera (17.2%), Cladocera (12.25%), C Ostracoda (8.5 %), Hemiptera (8.37%), O Copepoda (6.7%), Trichoptera (0.27 %) a (0.23%). Benthic diversity varied from a m June, 2009 to a maximum of 3.23 in Febru this ecosystem can be considered as m Rotifers and Diptera were dominant in thi attributed to their level of pollution toler species of these groups can tolerate high e of water and easily survive in polluted w and Plecoptera was totally absent thro period. This suggests that the study ar Mollusc and Plecoptera can’t tolerate hyp condition of aquatic ecosystem. The CO 2 w throughout the study period. Keywords Aquatic Ecosystem, Be Diversity, Sewage Pollution. I. INTRODUCTION The present study on this fresh water e effect of high level sewage pollution resu and natural activities on benthic diversit in view of the economic importance and interests in respect of wild life, fisheries water quality in order to ensure the sust natural resources. Benthic macro organisms that live on or inside the dep of a water body (Idowu and Ugwumb communities are widely used in the mo of pollution as the organisms are m integrate effects of pollutants over tim communities comprise a large numbe because of the varying sensitivities of sp possible to identify subtle effects of poll changes in community structure. Until f accepted methods for identifying changes have been relatively crude, usin number of species, diversity indices occurrence of opportunistic species, but of such stress indices Gray (1989) s indicate end-points rather than first eff induced change. Copyright © 2014 IJAIR, All right reserved 946 International Journal of Agriculture I Volume 2, Issue 6, wage Pollution on Benthic resh Water Ecosystem beeba A. Kabeer* and Saltanat Parveen Zoology, Aligarh Muslim University, Aligarh 202 002, Indi *E-mail: [email protected] on on the benthic tern region of U.P., y, 2009 – January, nvironment of the ned by sieving the sical sorting. A total re recorded. These bution to the total re Rotifers (30%), Coleoptera (8.9%), Oligochaetes (6.8%), and Ephemeroptera minimum of 3.11 in uary, 2009 therefore moderately polluted. is ecosystem may be rance because some eutrophic condition water. The Mollusc oughout the study rea is polluted and poxia and eutrophic was found to absent enthic Community, N ecosystem focused sulting from human ty. This ecosystem d inherent scientific s, flood control and tainable use of the fauna are those posit at the bottom ba, 2005). Benthic onitoring of effects mostly sessile and me. Most benthic er of species and pecies it should be llutants reflected in fairly recently, the pollution-induced ng changes in total and frequency of in a recent review suggests that they fects of pollution- Benthic communities are esp and evaluating the impacts of lo and aquatic contamination anoxia/hypoxia is greatest in hydrophobic anthropogenic accumulate in sediments. Bent mobility cannot avoid adverse c local environmental conditions fauna (Gray, 1979). The d tolerances, life history strateg trophic interactions can ma communities effective estim condition. Several papers co indices to assess the ecologica and estuarine environments (Bo al., 2008; Weisberg et al., 2 between the unavailable nutrie protein materials in fish and oth organisms feed on detritus that water and in turn serve as food (Idowu and Ugwumba, 200 breakdown of decaying orga organic forms such as phospha al., 1978). All forms of aquatic link of several food cha environments, can utilize the nu A highly diverse group, bent excellent candidates for studies Aquatic insects often make go are present in some capacity habitat and many are habita Gripenberg, 2008). Diversity attribute of a natural or organ related to other structural and fu productivity, niche structure, integration of the community. called biological diversity conservation in terrestrial, environments (Brooks et al., 20 II. MATERIAL AN Aquatic ecosystem directl enormous ecological, comme importance. They are rich in diversity like, flora and faun regional significance. Aligarh richly well off with hundreds o used as drainage basin and regular fisheries of various kin water sewage fed Pond is almos Manuscript Processing Details (dd/mm/yyyy Received : 05/05/2014 | Accepted on : 20/05 Innovations and Research , ISSN (Online) 2319-1473 c Diversity of ia pecially useful in detecting ow dissolved oxygen events because exposure to n near bottom waters and contaminants typically thic organisms with limited conditions and better reflect s compared to most pelagic diversity of physiological gies, feeding modes, and ake sedimentary benthic mators of environmental oncern the use of benthic al quality, status of marine orja et al., 2008; Teixeira et 2008). They form the link ents in detritus and useful her organisms. Most benthic t settle on the bottom of the d for a wide range of fishes 05). They accelerate the ganic matter into simpler ates and nitrates (Gallep et c plants, which are the first ains existing in aquatic utrients. thic macroinvertebrates are s of changes in biodiversity. ood indicators because they y in almost every type of at specialists (Lewis and is an important structural nized community, which is unctional properties such as competition, stability and The sustaining of the so- is a priority of nature marine and freshwater 006). ND METHODS ly or indirectly has an ercial and socio-economic n the components of bio- na of local, national and and its adjoining areas are of derelict ponds which are support an extensive and nd. This is a perennial fresh st rectangular in shape. It is y) : 5/2014 | Published : 24/05/2014

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Copyright © 2014 IJAIR, All right reserved

Effect of Waste Sewage

Fresh

Habeeba A. Kabeer* and Saltanat ParveenDepartment of Zoology, Aligarh Muslim University, Aligarh 202 002, India

Abstract – Effect of sewage pollution on the benthic

diversity of fresh water ecosystem of western region

India was carried out between February, 2009

2010, by investigating the biological environment of the

habitats. The faunal species were obtained by sieving the

sediment with 0.5mm mesh sieve and physical sorting. A total

of ten major taxonomic groupings were recorded. These

groupings and their percentage contribution to the total

macro-benthic organisms collection are

Diptera (17.2%), Cladocera (12.25%), Coleoptera (8.9%),

Ostracoda (8.5 %), Hemiptera (8.37%), Oligochaetes (6.8%),

Copepoda (6.7%), Trichoptera (0.27 %) and

(0.23%). Benthic diversity varied from a minimum of 3.11 in

June, 2009 to a maximum of 3.23 in Februar

this ecosystem can be considered as moderately polluted.

Rotifers and Diptera were dominant in this

attributed to their level of pollution tolerance

species of these groups can tolerate high eutrophic condit

of water and easily survive in polluted water

and Plecoptera was totally absent throughout the study

period. This suggests that the study area is polluted

Mollusc and Plecoptera can’t tolerate hypoxia and eutrophic

condition of aquatic ecosystem. The CO2 was found to absent

throughout the study period.

Keywords – Aquatic Ecosystem, Benthic Community,

Diversity, Sewage Pollution.

I. INTRODUCTION

The present study on this fresh water ecosystem focused

effect of high level sewage pollution resulting from human

and natural activities on benthic diversity

in view of the economic importance and inherent scientific

interests in respect of wild life, fisheries, flood control and

water quality in order to ensure the sustainable use of the

natural resources. Benthic macro fauna are those

organisms that live on or inside the deposit at the bottom

of a water body (Idowu and Ugwumba, 2005).

communities are widely used in the monitoring of effects

of pollution as the organisms are mostly sessile and

integrate effects of pollutants over time. Most benthic

communities comprise a large number of species and

because of the varying sensitivities of species it should be

possible to identify subtle effects of pollutants

changes in community structure. Until fairly recently, the

accepted methods for identifying pollution

changes have been relatively crude, using changes in total

number of species, diversity indices and frequency of

occurrence of opportunistic species, but in a recent review

of such stress indices Gray (1989) suggests that they

indicate end-points rather than first effects of pollution

induced change.

Copyright © 2014 IJAIR, All right reserved

946

International Journal of Agriculture Innovations and Research

Volume 2, Issue 6, ISSN

ewage Pollution on Benthic

resh Water Ecosystem

Habeeba A. Kabeer* and Saltanat Parveen Department of Zoology, Aligarh Muslim University, Aligarh 202 002, India

*E-mail: [email protected]

pollution on the benthic

of fresh water ecosystem of western region of U.P.,

carried out between February, 2009 – January,

2010, by investigating the biological environment of the

The faunal species were obtained by sieving the

sediment with 0.5mm mesh sieve and physical sorting. A total

ere recorded. These

groupings and their percentage contribution to the total

collection are Rotifers (30%),

Cladocera (12.25%), Coleoptera (8.9%),

Ostracoda (8.5 %), Hemiptera (8.37%), Oligochaetes (6.8%),

and Ephemeroptera

diversity varied from a minimum of 3.11 in

June, 2009 to a maximum of 3.23 in February, 2009 therefore

can be considered as moderately polluted.

his ecosystem may be

attributed to their level of pollution tolerance because some

species of these groups can tolerate high eutrophic condition

of water and easily survive in polluted water. The Mollusc

and Plecoptera was totally absent throughout the study

This suggests that the study area is polluted and

Mollusc and Plecoptera can’t tolerate hypoxia and eutrophic

was found to absent

Aquatic Ecosystem, Benthic Community,

NTRODUCTION

fresh water ecosystem focused

resulting from human

on benthic diversity. This ecosystem

in view of the economic importance and inherent scientific

interests in respect of wild life, fisheries, flood control and

e sustainable use of the

Benthic macro fauna are those

organisms that live on or inside the deposit at the bottom

of a water body (Idowu and Ugwumba, 2005). Benthic

communities are widely used in the monitoring of effects

the organisms are mostly sessile and

integrate effects of pollutants over time. Most benthic

communities comprise a large number of species and

because of the varying sensitivities of species it should be

possible to identify subtle effects of pollutants reflected in

changes in community structure. Until fairly recently, the

accepted methods for identifying pollution-induced

changes have been relatively crude, using changes in total

number of species, diversity indices and frequency of

unistic species, but in a recent review

of such stress indices Gray (1989) suggests that they

points rather than first effects of pollution-

Benthic communities are especially useful in detecting

and evaluating the impacts of lo

and aquatic contamination because exposure to

anoxia/hypoxia is greatest in near bottom waters and

hydrophobic anthropogenic contaminants typically

accumulate in sediments. Benthic organisms with limited

mobility cannot avoid adverse conditions and better reflect

local environmental conditions compared to most pelagic

fauna (Gray, 1979). The diversity of physiological

tolerances, life history strategies, feeding modes, and

trophic interactions can make sedimentary benthic

communities effective estimators of environmental

condition. Several papers concern the use of benthic

indices to assess the ecological quality, status of marine

and estuarine environments (Borja

al., 2008; Weisberg et al., 2008).

between the unavailable nutrients in detritus and useful

protein materials in fish and other organisms. Most benthic

organisms feed on detritus that settle on the bottom of the

water and in turn serve as food for a wide range of fishes

(Idowu and Ugwumba, 2005). They accelerate the

breakdown of decaying organic matter into simpler

organic forms such as phosphates and nitrates (Gallep

al., 1978). All forms of aquatic plants, which are the first

link of several food chains existing in aquatic

environments, can utilize the nutrients.

A highly diverse group, benthic macroinvertebrates are

excellent candidates for studies of changes in biodiversity.

Aquatic insects often make good indicators because they

are present in some capacity in almost every

habitat and many are habitat specialists (Lewis and

Gripenberg, 2008). Diversity is an important structural

attribute of a natural or organized community, which is

related to other structural and functional properties such as

productivity, niche structure, competition, stability and

integration of the community. The sustaining of the so

called biological diversity is a priority of nature

conservation in terrestrial, marine and freshwater

environments (Brooks et al., 2006).

II. MATERIAL AND

Aquatic ecosystem directly or indirectly has

enormous ecological, commercial and socio

importance. They are rich in the components of bio

diversity like, flora and fauna of local, national and

regional significance. Aligarh and its adjoining areas are

richly well off with hundreds of derelict ponds which are

used as drainage basin and support an extensive and

regular fisheries of various kind. This is a perennial fresh

water sewage fed Pond is almost rectangular in sh

Manuscript Processing Details (dd/mm/yyyy) :

Received : 05/05/2014 | Accepted on : 20/05

International Journal of Agriculture Innovations and Research

, ISSN (Online) 2319-1473

enthic Diversity of

Department of Zoology, Aligarh Muslim University, Aligarh 202 002, India

Benthic communities are especially useful in detecting

and evaluating the impacts of low dissolved oxygen events

and aquatic contamination because exposure to

anoxia/hypoxia is greatest in near bottom waters and

hydrophobic anthropogenic contaminants typically

accumulate in sediments. Benthic organisms with limited

rse conditions and better reflect

local environmental conditions compared to most pelagic

fauna (Gray, 1979). The diversity of physiological

tolerances, life history strategies, feeding modes, and

trophic interactions can make sedimentary benthic

es effective estimators of environmental

condition. Several papers concern the use of benthic

indices to assess the ecological quality, status of marine

and estuarine environments (Borja et al., 2008; Teixeira et

., 2008). They form the link

between the unavailable nutrients in detritus and useful

protein materials in fish and other organisms. Most benthic

organisms feed on detritus that settle on the bottom of the

water and in turn serve as food for a wide range of fishes

nd Ugwumba, 2005). They accelerate the

breakdown of decaying organic matter into simpler

organic forms such as phosphates and nitrates (Gallep et

., 1978). All forms of aquatic plants, which are the first

link of several food chains existing in aquatic

nvironments, can utilize the nutrients.

A highly diverse group, benthic macroinvertebrates are

excellent candidates for studies of changes in biodiversity.

Aquatic insects often make good indicators because they

are present in some capacity in almost every type of

habitat and many are habitat specialists (Lewis and

Gripenberg, 2008). Diversity is an important structural

attribute of a natural or organized community, which is

related to other structural and functional properties such as

tructure, competition, stability and

integration of the community. The sustaining of the so-

called biological diversity is a priority of nature

conservation in terrestrial, marine and freshwater

., 2006).

ATERIAL AND METHODS

ecosystem directly or indirectly has an

enormous ecological, commercial and socio-economic

importance. They are rich in the components of bio-

diversity like, flora and fauna of local, national and

Aligarh and its adjoining areas are

richly well off with hundreds of derelict ponds which are

used as drainage basin and support an extensive and

regular fisheries of various kind. This is a perennial fresh

water sewage fed Pond is almost rectangular in shape. It is

Manuscript Processing Details (dd/mm/yyyy) :

5/2014 | Published : 24/05/2014

Copyright © 2014 IJAIR, All right reserved

shallow pond. Its source of water replenishment is mainly

sewage effluent from Medical College through drains, the

overhead tank and surface run-off from surrounding areas.

Many washermen use this pond for washing clothes, thus

adding certain chemicals and colour to its water almost

every day that brings certain pysico

biological changes in its flora and fauna regularly. The

water of the pond is turbid due to luxuriant growth of

microscopic algae, colour stains and washing chemicals

used by washermen. Bottom of the pond contains mostly

loose mud, sand, stones, part of dead plants, dead plankton

and decayed littler deposited by trees situated on its bank.

A. Sediment analysis and Water analysisSampling of sediment and water was

February, 2009 to January, 2010. At each sampling site

sediment sample was collected using Ekman

water sample in bottle after collection labeled and bring to

laboratory. The collected sediment was washed and sieved

on a mesh screen of 0.5 mm preserved and identify under

microscope. The Benthic macro-invertebrates were

identified using identification keys Edmondson (1959),

Pennak (1978) and Tonapi (1980) and density determined

per meter square area (ind/m2). The conductivity and pH

were measured using a digital conductivity meter,

Dissolved oxygen, (TS), (TDS), (TS

Hardness, Calcium, Magnesium and Nitrate

(NO3-N), Phosphate- phosphorus (PO4-

Free carbon dioxide (CO2), composition of sand, silt a

clay and Organic matter and organic carbon were analyzed

according to the method given by Triedy and Goel (1984),

Barnes (1959), Michael (1984).

B. Statistical analyses Patterns of spatial and seasonal variation of Benthic

macro-invertebrates population with environmental

variables were described using Correspon

Analysis (CCA) with the help of Past

Harper (2001) and diversity indices, MDS and

dendogram were calculated and plotted with the

help of Primer v5 (version 5.2.4).

III. RESULT AND DISCUSSION

The percentage compositions of each of the major

benthic fauna are presented in Table 1. A total of

major taxonomic groupings were recorded. These

groupings and their percentage contribution to the total

macro-benthic collection are Rotifers (30%), Diptera

(17.2%), Cladocera (12.25%), Coleoptera (8.9%),

Ostracoda (8.5 %), Hemiptera (8.37%), Oligochaetes

(6.8%), Copepoda (6.7%), Trichoptera (0.27 %) and

Ephemeroptera (0.23%) (Table-I) were recorded in the

study area. The Shannon Wiener index is based on both

the number of species present and relative abundance of

each species. Monthly benthos species diversity is given in

Table II. The index values for benthic

from a minimum of 3.11 in June, 2009 to a maximum of

3.23 in February, 2009 and Menhinicks index of diversity

for benthos varied from a minimum of 0.553 in December,

2009 to a maximum of 0.786 in July, 2009

Shannon – Weiner diversity index proposed as diversity

Copyright © 2014 IJAIR, All right reserved

947

International Journal of Agriculture Innovations and Research

Volume 2, Issue 6, ISSN

shallow pond. Its source of water replenishment is mainly

sewage effluent from Medical College through drains, the

off from surrounding areas.

Many washermen use this pond for washing clothes, thus

emicals and colour to its water almost

every day that brings certain pysico-chemical and

biological changes in its flora and fauna regularly. The

water of the pond is turbid due to luxuriant growth of

microscopic algae, colour stains and washing chemicals

used by washermen. Bottom of the pond contains mostly

loose mud, sand, stones, part of dead plants, dead plankton

and decayed littler deposited by trees situated on its bank.

and Water analysis ampling of sediment and water was performed from

February, 2009 to January, 2010. At each sampling site

sediment sample was collected using Ekman-dredges and

water sample in bottle after collection labeled and bring to

laboratory. The collected sediment was washed and sieved

preserved and identify under

invertebrates were

identified using identification keys Edmondson (1959),

Pennak (1978) and Tonapi (1980) and density determined

The conductivity and pH

were measured using a digital conductivity meter,

Dissolved oxygen, (TS), (TDS), (TS-TDS=TSS),

Hardness, Calcium, Magnesium and Nitrate-nitrogen

-P), Alkalinity and

), composition of sand, silt and

clay and Organic matter and organic carbon were analyzed

according to the method given by Triedy and Goel (1984),

Patterns of spatial and seasonal variation of Benthic

population with environmental

variables were described using Correspondence Canonical

with the help of Past by Hammer and

diversity indices, MDS and

were calculated and plotted with the

ISCUSSION

The percentage compositions of each of the major

benthic fauna are presented in Table 1. A total of ten

were recorded. These

contribution to the total

Rotifers (30%), Diptera

(17.2%), Cladocera (12.25%), Coleoptera (8.9%),

Ostracoda (8.5 %), Hemiptera (8.37%), Oligochaetes

(6.8%), Copepoda (6.7%), Trichoptera (0.27 %) and

were recorded in the

The Shannon Wiener index is based on both

the number of species present and relative abundance of

each species. Monthly benthos species diversity is given in

ic diversity varied

2009 to a maximum of

3.23 in February, 2009 and Menhinicks index of diversity

for benthos varied from a minimum of 0.553 in December,

2009 to a maximum of 0.786 in July, 2009 (Table II). The

Weiner diversity index proposed as diversity

index > 4 is clean water; between 3

water and < 2 is heavily polluted water (Shekhar

2008). Since, the Shannon-Weiner diversity index in the

present study ranged between 3.11

water ecosystem; they can be considered as moderately

polluted. Moreover, diversity and evenness followed the

same trend in selected study area

always associated with high evenness (Ismail and

Dorgham, 2003). Sorenson’s index va

similarity) for Similarity index between different months

of the recorded benthic groups is depicted in dendrogram

and MDS (Fig. I). The highest similarity was recorded in

April, 2009 – August, 2009 and

July, 2009 – December, 2009

Similarity index values suggest that most of the species in

this ecosystem were common during the course of stud

This has resulted in overlapping of faunal grouping and

predictability of community composition.

Canonical correspondence analysis (CCA) of benthic

community and water and sediment quality variables were

drawn up in the form of one matrix and were anal

canonical correspondence analysis (CCA) using PAST

program, version (2.10) by Hammer and Harper (2001).

CCA diagram was performed to determine relationships

between 20 environmental variables and 10 groups of

benthos. It is a non-linear technique u

variations in the environmental factors. Benthic data were

log transformed to approach the assumed condition of

normality and homoscedasticity of the data to standardize

the data sets. The constrained ordination axis corresponds

to the direction of the greatest variability of the data set

that can be explained by the variables.

environmental factors are indicated by the length of arrow,

length of line represents the degree of relationship

between benthic groups and environmental fact

angle between arrow shaft and ordination axis indicates

the degree of correlation between environmental factors.

In addition the analysis make vertical lines connecting a

particular group with the line of environmental factors,

closer the connecting point on the line of environmental

factors to arrow shows stronger positive correlation.

Distribution pattern of groups in benthic community are

represented by points, points of group and environmental

factors indicates the distribution of groups and

characteristics of benthic community variance along the

gradient direction of each environmental factor.

The eigen value, value of p and Cumulative percentage

variance of groups-environment relation of axes 1

given the (Fig-II). Trichoptera and Hemiptera showed

positive correlation with Dissolved oxygen whereas

Diptera showed high positive correlation with Clay

composition and Alkalinity. Copepoda showed high

positive correlation with Clay, Sand, Chloride, pH and

Mg. Other groups like Rotifera, Oligochaeta and

Ephemeroptera showed high negative correlation with

Water temperature, Nitrate, Hardness, TDS, % Organic

matter, TS and Conductivity and Cladocera, Coleoptera

and Ostracoda showed high positive correlation with

Transparency, TSS, depth and Composition of Silt. CCA

analysis indicates that, in this aquatic ecosystem important

International Journal of Agriculture Innovations and Research

, ISSN (Online) 2319-1473

is clean water; between 3-4 is mildly polluted

water and < 2 is heavily polluted water (Shekhar et al.,

Weiner diversity index in the

present study ranged between 3.11– 3.23 in the selected

water ecosystem; they can be considered as moderately

polluted. Moreover, diversity and evenness followed the

study area. High diversity was

always associated with high evenness (Ismail and

orenson’s index values (% species

Similarity index between different months

of the recorded benthic groups is depicted in dendrogram

e highest similarity was recorded in

and lowest similarity was in

December, 2009 (Fig. I). Overall high

Similarity index values suggest that most of the species in

were common during the course of study.

This has resulted in overlapping of faunal grouping and

predictability of community composition.

Canonical correspondence analysis (CCA) of benthic

community and water and sediment quality variables were

drawn up in the form of one matrix and were analysed by

canonical correspondence analysis (CCA) using PAST

program, version (2.10) by Hammer and Harper (2001).

CCA diagram was performed to determine relationships

between 20 environmental variables and 10 groups of

linear technique used to relate

variations in the environmental factors. Benthic data were

log transformed to approach the assumed condition of

normality and homoscedasticity of the data to standardize

the data sets. The constrained ordination axis corresponds

ion of the greatest variability of the data set

n be explained by the variables. In graph,

environmental factors are indicated by the length of arrow,

length of line represents the degree of relationship

between benthic groups and environmental factors, the

angle between arrow shaft and ordination axis indicates

the degree of correlation between environmental factors.

In addition the analysis make vertical lines connecting a

particular group with the line of environmental factors,

ng point on the line of environmental

factors to arrow shows stronger positive correlation.

Distribution pattern of groups in benthic community are

represented by points, points of group and environmental

factors indicates the distribution of groups and

aracteristics of benthic community variance along the

gradient direction of each environmental factor.

The eigen value, value of p and Cumulative percentage

environment relation of axes 1-4 are

Trichoptera and Hemiptera showed

positive correlation with Dissolved oxygen whereas

Diptera showed high positive correlation with Clay

composition and Alkalinity. Copepoda showed high

positive correlation with Clay, Sand, Chloride, pH and

like Rotifera, Oligochaeta and

Ephemeroptera showed high negative correlation with

Water temperature, Nitrate, Hardness, TDS, % Organic

matter, TS and Conductivity and Cladocera, Coleoptera

and Ostracoda showed high positive correlation with

TSS, depth and Composition of Silt. CCA

analysis indicates that, in this aquatic ecosystem important

Copyright © 2014 IJAIR, All right reserved

factors affecting benthos distribution are Water

temperature, Dissolved oxygen, Nitrate, Phosphate,

Alkalinity, Calcium, Magnesium, Transparency, Chloride,

Depth, Total dissolved solids, Total suspended solids,

Total solids, % Organic matter, Composition of Silt and

Clay. However, pH, Hardness, Conductivity and

composition of Sand have a lesser influences on the

distribution of the benthic species. The diffe

species composition and abundance may be attributed to

the ecological differences of the different habitat locations

and period of investigation water quality, immediate

substrate for occupation and food availability may also

affect the abundance and distribution of the

macroinvertebrates communities. The numerical numbers

of the individual species recorded in this study were high.

This suggests that they can survive eutrophic condition of

water.

Table I: Monthly abundance (No/m

Fig.I. Dendogram and MDS showing similarity of Benthic community between

Copyright © 2014 IJAIR, All right reserved

948

International Journal of Agriculture Innovations and Research

Volume 2, Issue 6, ISSN

factors affecting benthos distribution are Water

temperature, Dissolved oxygen, Nitrate, Phosphate,

Alkalinity, Calcium, Magnesium, Transparency, Chloride,

Depth, Total dissolved solids, Total suspended solids,

Total solids, % Organic matter, Composition of Silt and

Clay. However, pH, Hardness, Conductivity and

composition of Sand have a lesser influences on the

The differences in

composition and abundance may be attributed to

ecological differences of the different habitat locations

and period of investigation water quality, immediate

substrate for occupation and food availability may also

and distribution of the

The numerical numbers

recorded in this study were high.

they can survive eutrophic condition of

IV. CONCLUSION

� The absence of Mollusk and

study area showed eutrophic condition

survive in polluted water because

their filter feeding mechanism which is blocked in

polluted and high turbid water

at low oxygen concentration (hypoxia).

� The Shannon-Weiner diversity index in the present

study ranged between 3.11–

ecosystem; they can be considered as moderately

polluted.

� The numerical numbers of the individual species

recorded in this study were high this may be attributed

to their level of pollution tolerance.

� The CO2 was found to absent throughout the study

period might be attributed due to its utilization in

photosynthesis process as well as conversion in to

carbonate and bicarbonate.

aquatic ecosystem is polluted presently.

Monthly abundance (No/m2) and percent contribution of Benthic community

Fig.I. Dendogram and MDS showing similarity of Benthic community between different months

International Journal of Agriculture Innovations and Research

, ISSN (Online) 2319-1473

ONCLUSION

Mollusk and Plecoptera throughout the

showed eutrophic condition and they can’t

because Mollusk can’t feed by

their filter feeding mechanism which is blocked in

water. Plecoptera can’t survive

n concentration (hypoxia).

Weiner diversity index in the present

– 3.23 in the selected water

ecosystem; they can be considered as moderately

The numerical numbers of the individual species

study were high this may be attributed

to their level of pollution tolerance.

was found to absent throughout the study

period might be attributed due to its utilization in

photosynthesis process as well as conversion in to

. This suggests that this

polluted presently.

) and percent contribution of Benthic community

different months

Copyright © 2014 IJAIR, All right reserved

Axis

1

2

3

4

Fig.II: Canonical correspondence analysis (CCA) diagram of 20 environmental parameters (Water temperature

pH, Dissolved-oxygen- DO, Nitrate-

Transparency-TR, Chloride-CH, Conductivity

Total solids-TS, % organic matter-OM, composition of Sand

Copepoda-CP, Ostracoda-OS, Rotifera

Table II: Monthly variation in Species Diversity and

Species Evenness of benthos

Months Species Diversity Menhinick Index

Feb, 09 3.236

Mar 3.205

Apr 3.216

May 3.169

Jun 3.115

Jul 3.205

Aug 3.224

Sep 3.217

Oct 3.178

Nov 3.192

Dec 3.203

Jan, 10 3.141

Copyright © 2014 IJAIR, All right reserved

949

International Journal of Agriculture Innovations and Research

Volume 2, Issue 6, ISSN

Eigenval p

0.01699 0.3069

0.007541 0.1584

0.006264 0.08911

0.005375 0.3861

Canonical correspondence analysis (CCA) diagram of 20 environmental parameters (Water temperature

-N, Phosphate-P, Alkalinity-AL, Hardness-HR, Calcium

CH, Conductivity-CN, Depth-D, Total dissolved solids-TD, Total suspended solids

OM, composition of Sand-Sa, Silt-Si, Clay-Cy) and 10 benthic groups(Cladocera

OS, Rotifera-RT, Oligochaeta-OL, Diptera-DI, Coleoptera-CO, Hemiptera

TR and Ephemeroptera-EP)

Monthly variation in Species Diversity and

Species Evenness of benthos

Menhinick Index

0.6089

0.6221

0.6751

0.6626

0.6668

0.7865

0.718

0.68

0.6171

0.6254

0.5537

0.5554

ACKNOWLEDGMENTS

Authors are highly thankful to the Chairman, Dept. of

Zoology, A.M.U. Aligarh for providing laboratory

facilities.

REFERENCES

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Pilgrim, J. D and Rodrigues, A. S. L. 2006. Global

BiodiversityConservation Priorities.

International Journal of Agriculture Innovations and Research

, ISSN (Online) 2319-1473

%

40.35

17.91

14.88

12.77

Canonical correspondence analysis (CCA) diagram of 20 environmental parameters (Water temperature-WR, pH-

HR, Calcium-Ca, Magnesium-Mg,

TD, Total suspended solids-TSS,

Cy) and 10 benthic groups(Cladocera-CL,

CO, Hemiptera-HE, Trichoptera-

CKNOWLEDGMENTS

Authors are highly thankful to the Chairman, Dept. of

A.M.U. Aligarh for providing laboratory

EFERENCES

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Pilgrim, J. D and Rodrigues, A. S. L. 2006. Global

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Copyright © 2014 IJAIR, All right reserved

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AUTHOR’S PROFILE

Dr. Habeeba Ahmad M. Phil and P.hD from Aligarh Muslim University,

Aligarh, U.P., India

Email: [email protected]

Copyright © 2014 IJAIR, All right reserved

950

International Journal of Agriculture Innovations and Research

Volume 2, Issue 6, ISSN

Ward and Whipple’s Freshwater

Ed. John Wiley & Sons Inc., New York, 1248 pp.

.F. Kitchell and S.M. Bartell, 1978. Phosphorous

release from lake sediments as affected by chironomid. Ver.

1989. Effects of environmental stress on species rich

32.

Hammer, O., Harper, D.A.T. and Ryan, P.D. 2001. PAST:

Paleontological statistics software package for education and

, 4(1): 9.

. Physical chemical and

faunal characteristics of a southern Nigeria reservoir. Zoologist,

Ismail, A.A. and Dorgham, M. M. (2003) – Ecological indices as

Dehaila Harbor (Alexandria,

Lewis, O.T. and Gripenberg, S. 2008. Insect seed predators and

Journal of Applied Ecology, 45 (6): 1593-

Ecological methods for field and laboratory

McGraw Hill Publication

Freshwater invertebrates of United States.

Ed. Johan Wiley and Sons Inc., New York, 803 pp.

Shekhar, S. T. R., Kiran, B. B., Puttaiah, E. T., Shivraj. Y. and

Phytoplankton as index of water

quality with reference to industrial pollution. Journ. Environ.

, Neto, J.M. and Marques, J.C.

A benthic perspective in assessing the ecological status of

estuaries: the case of the Mondego Estuary (Portugal). Ecol.

Fresh water animals of India. Oxford and

Chemical and biological

Karad, India; 215 pp.

Weisberg, S.B., Thompson, B., Ranasinghe, J.A., Montagne,

D.E., Cadien, D.B., Dauer, D.M., Diener, D., Oliver, J., Reish,

The level of agreement

among experts applying best professional judgment to assess the

condition of benthic infaunal communities. Ecological

r. Habeeba Ahmad Kabeer

M. Phil and P.hD from Aligarh Muslim University,

Email: [email protected]

International Journal of Agriculture Innovations and Research

, ISSN (Online) 2319-1473