Journal of Marine Sciences

Journal of Marine Sciences / 2015 / Article

Research Article | Open Access

Volume 2015 |Article ID 376986 |

A. I. Inyang, K. E. Sunday, D. I. Nwankwo, "Composition of Periphyton Community on Water Hyacinth (Eichhornia crassipes): In Analysis of Environmental Characteristics at Ejirin Part of Epe Lagoon in Southwestern Nigeria", Journal of Marine Sciences, vol. 2015, Article ID 376986, 9 pages, 2015.

Composition of Periphyton Community on Water Hyacinth (Eichhornia crassipes): In Analysis of Environmental Characteristics at Ejirin Part of Epe Lagoon in Southwestern Nigeria

Academic Editor: Robert A. Patzner
Received07 Sep 2014
Revised24 Nov 2014
Accepted04 Dec 2014
Published08 Jan 2015


The composition of periphyton community on water hyacinth was investigated at Ejirin, part of Epe Lagoon, in relation to environmental characteristics from December 2012 to May 2013. A total of 14,536 individuals of 104 species belonging to five divisions were identified, with Bacillariophyta (82.69%), Cyanobacteria (10.43%), Chlorophyta (5.63%), and Euglenophyta (1.15%). The total species abundance observed showed a strong correlation with rainfall () and strongly significant correlation with TDS (; ). Biochemical oxygen demand value remained (BOD) 4.8 mg/L while Shannon-Wiener index value remained (. The presence of the following organisms could be used as an indicator of environmentally stressed aquatic ecosystem: euglenoids, blue green algae, Nitzschia palea, Surirella sp., Pinnularia sp., Gomphonema parvulum, Mougeotia sp., Spirogyra sp., Trachelomonas affinis (Lemm.), and T. ensifera Daday; T. gibberosa Playf. and Phormidium articulatum; Lyngbya intermedia; Cymbella ventricosa; Eunotia arcus; Surirella linearis and Closterium parvulum Nag.

1. Introduction

Water hyacinth (Eichhornia crassipes) was introduced into the Nigerian coastal waters in September 1984 from Porto Novo Creek (Benin Republic) and has continued to flourish. Schlorin [1] stated that water hyacinth is a sensitive indicator of environmental status of certain tropical waters. Water hyacinth plant provides suitable surfaces for the development of periphyton as well as aquatic fauna on floating leaves, hanging roots, and creeping stems. According to Egborge [2], water hyacinth harbours a variety of organisms which include algae, rotifers, nematodes, annelids, molluscs, hydracerids, cladocerans, copepod, conchostracans, isopod, amphipods, crabs, and fishes. Organisms such as snails and mayflies affect the periphyton species assemblage, biomass, and productivity [3].

The algae found in water bodies depend on cells, which may either float on the surface or grow on submerged objects, and are divided into two groups, namely, phytoplankton and periphyton [4, 5]. The term “periphyton,” coined by Behning and Cooke [6, 7], was derived from two Greek words, “peri,” meaning “round,” and “phyton,” meaning plant. Periphyton has become a universally accepted expression for all organisms that are attached to a submerged substrate and generally dominated by photosynthetic organism which may be unicellular, colonial, or filamentous species from a variety of prokaryotic and eukaryotic phyla. As applied to this work, Wetzel [8] defined periphyton as the micro- “floral” community living attached to the substrate inside water. This microfloral community plays an important role in water bodies, not only by being important primary producers [9, 10] and serving as an energy source for higher trophic level [11], but also by affecting the nutrient turnover [12] and the transfer of nutrients between the benthic and the pelagic zone [13]. Several works on substrate-mediated effect on periphyton biomass and composition have been reported [14, 15] and its usage as an important indicator of the health of aquatic systems [1618]. These organisms are useful indicator groups for pollution bioassessment due to their sensitivity to pollution. Since the composition of periphyton community on water hyacinth at Ejirin has not been assessed, it is therefore important to document its composition and abundance in relation to environmental characteristics. This study will serve as a source of data background and information on water quality and periphyton abundance and composition.

1.1. Study Area

The study site, Ejirin (Figure 1), located (6°89′′N, 3°38′′E) is part of Epe Lagoon, freshwater and nontidal lagoon. It is sandwiched between Lekki Lagoon to the east and Lagos Lagoon to the west. It experiences the same hydroclimatic conditions as the rest of southwestern Nigeria such that there are two main seasons (wet and dry). The littoral vegetation found there is dominantly Raffia palm and some dotted mangrove, while on surface water some floating macrophyte like water hyacinth (Eichhornia crassipes) dominates. The people there are mainly artisanal fishermen, sand miners, and petty traders.

2. Materials and Methods

2.1. Physicochemical Characteristics

Water samples were collected on each trip between 09:00 and 13:00 and stored in 250 mL well labelled plastic bottles and transported to the laboratory in an ice chest. Surface water temperatures were measured in situ using a mercury-in-glass thermometer and recorded to the nearest 0.1°C. Transparency was determined using 20 cm white painted Secchi disc while pH values were measured using a Graffin digital pH meter. Dissolved oxygen concentration was determined by unmodified Winkler method [19], conductivity was assessed using the meter (Philips PW9505), and chemical oxygen demand and biochemical oxygen demand values were determined using the method described in APHA [20]. Reactive nitrogen, reactive phosphorus, sulphate, and silicate were measured as described by APHA [20]. Rainfall data was obtained from the Federal Meteorological Department, Oshodi, Lagos.

2.2. Determination of Periphyton Biomass

Healthy plants were carefully selected to ensure uniformity in size before putting each into plastic containers with 500 mL of tap water. The attached algae were removed mechanically by shaking vigorously in water as suggested by Foerster and Schlichting [21] and preserved in a well labelled plastic container with 4% unbuffered formalin added to fix the periphyton sample. Another 500 mL container was filled with an unfixed sample for chlorophyll analysis. Chlorophyll was determined by fluorometric method as described by APHA [20].

2.3. Analysis of Biological Characteristics

Periphyton samples were thoroughly investigated using CHA and CHB binocular microscope with a calibrated eye piece, noting all fields. Counting was done using a microtransect drop count, and 10 drops of periphyton samples were investigated for each month as described by [22]. All organisms, unicels, filaments, and coenobia were counted as one and recorded as per mL. Appropriate texts such as [2326] (Biggs and Kilroy) were used to aid in the identification of periphyton. Two community structure parameters were used to determine possible response of the periphyton flora to environmental stress. These were as follows.

(i) Shannon-Wiener diversity index (), proposed by Shannon-Wiener in 1963: it is given by where is Shannon-Wiener index, is the total number of individuals in the population, is proportion that the th species represent the total number of individuals in the sampling space, is summation, and represents counts denoting th species ranging from 1 to .

(ii) Species richness index (), proposed by Margalef in 1951: it is given by where is species richness index, is the number of species in the population, and is the total number of individuals in species.

2.4. Statistical Analysis

Statistical analysis was carried out with the aid of SPSS (version 17) and PAST (version 3) statistical tools. Correction coefficient [27] was used to evaluate relationship between periphyton abundance and some environmental variables (temperature, salinity, total monthly rainfall, TDS, TSS, transparency, pH, and micronutrients). It is given by Spearman rank correlation: where is the correlation coefficient, is the sum of squares of difference of the ranks, and is the number of months.

-test analysis was carried out to evaluate statistical difference () in seasonal (wet and dry) abundance of periphyton community. Standard deviation and mean analysis were also evaluated.

3. Result

The data for physicochemical features at Ejirin Creek from December 2012 to May 2013 showed seasonal variation as presented in Table 1. Surface water temperature peaked 33.01°C in May and lower value of 28°C in January with a mean value of 30°C. The surface water temperature showed a strong significant correlation with rainfall (; ) (Table 3). The surface water pH was acidic throughout the sampling period (pH ≤ 6.6) with a mean value of 6.39. Conductivity peaked 0.35 μs/cm in May and lower value of 0.006 μs/cm in March, with a mean value of 0.184 μs/cm. Conductivity showed a strong positive correlation with rainfall () and with periphyton chlorophyll (). Transparency values were high in the dry months and low in the wet months. This corresponds to the rainfall pattern encountered during the study. The water remained fresh throughout the study period with salinity value .

ParametersDecemberJanuaryFebruaryMarchApril MayMeanStandard deviation

Water temp. (°C)29.328.32930.629.333.129.931.72
Transparency (cm)435741.538.5343140.89.11
Depth (cm)25283027302627.72.07
Conductivity (µs/cm)0.1920.1540.20.0060.20.350.180.11
TSS (mg/L)55661707311.161.0162.09
TDS (mg/L)0.65798714111916197.9456.95
Rainfall (mm)13.202850.1165.3340.899.57132.25
Salinity ()0000.01000.0020.004
Nitrate (mg/L)0.320.
Phosphate (mg/L)0.780.650.591.080.710.590.730.18
Sulphate (mg/L)1.200.801.261.301.
Silicate (mg/L)0.40 0.800.
Periphyton chl. a (mg/L)0.0030.0010.0030.0030.00230.00096
Biological oxygen demand (mg/L)4.80.423.
Chemical oxygen demand (mg/L)15162037323225.339.46
Dissolved oxygen (mg/L)6.13104.555.866.241.95

The micronutrients varied throughout the study periods with reactive nitrate (NO3-N ≤ 0.32), reactive phosphate (PO4-P ≤ 0.78), silicate (SiO3 ≤ 0.80), and sulphate (≤1.30). Periphyton chlorophyll reached a peak value (0.003 mg/L) recorded in February and April while its lower value (0.001 mg/L) was recorded in March, with a mean value of 0.0023 mg/L. Biochemical oxygen demand reached a peak value (4.8 mg/L) recorded in December and the lowest value (0.4 mg/L) was recorded in January, with a mean value of 2.317 mg/L. Chemical oxygen demand value ranged between 15 mg/L (December) and 37 mg/L (March), with a mean value of 2.31 mg/L. Dissolved oxygen demand (DO) value reached a peak value (10 mg/L) recorded in January and a lower value (4.5 mg/L) was recorded in February, with a mean value of 6.24 mg/L.

The checklist of the periphyton species between December 2012 and May 2013 is presented in Table 2. A total of 14, 536 individuals of 104 species were recorded throughout the study period. The total number of taxa varied from 24 in December to 26 in January, 23 in February, 63 in March, 41 in April, and 49 in May. Diatom populations during both seasons were dominated by 10 centric diatoms and 34 pennate diatoms and a total of 19 species were recorded for Cyanobacteria. Five divisions were recorded with their percentage of occurrence: Bacillariophyta (82.69%), Cyanobacteria (10.43%), Chlorophyta (5.63%), and Euglenophyta (1.15%). The total amount of periphyton abundance shows a strong positive correlation with water temperature (), pH (), rainfall (), and sulphate (). It also strongly correlates significantly with TDS (; ) and with transparency (; ). There was greater species richness during wet months than dry months with a value . Shannon-Wiener diversity index value was observed to be (Table 4).

Periphyton taxaDecember

Phylum: Cyanophyta
 Class: Cyanophyceae
  Order I: Chroococcales
   Chroococcus major 2447
   Chroococcus gardneri 2323
   Chroococcus occidentalis 28
   Chroococcus deltoids 51
   Chroococcus mediocris 3337
   Chroococcus mipitanensis 36
   Merismopedia punctata Meyen721
   Chlorella subsala Lemm.14
   Chlorogloea gardneri 23
   Cyanothece sp. 14
   Gomphosphaeria sp.22
   Aphanocapsa conferta 4332
   Anacystis sp.14
   Aphanothece comasii 22
   Aphanothece variabilis 8
  Order II: Nostocales
   Anabaena sp. Bory ex Bornet42183746
  Order III: Oscillatoriales
   Lyngbya intermedia Agardh ex Gomont58179147201187
   Phormidium articulatum 4234
   Komvophoron sp. 18
Phylum: Euglenophyta
 Class: Euglenophyceae
  Order I: Euglenales
   Euglena oxyuris var. charkowiensis 813811
   Euglena gracilis Klebs12
   Phacus orbicularis Hubner14
   Phacus caudatus Hubner13
   Phacus triqueter 13
   Trachelomonas affinis (Lemm.)1212
   Trachelomonas ensifera Daday916
   Trachelomonas gibberosa Playf.1313
Phylum: Bacillariophyta
 Class: Bacillariophyceae
  Order I: Centrales
   Aulacoseira granulata var. angustissima f. curvata Simon17241301342407524
   Aulacoseira granulate var. angustissima f. spiralis O. Mull.181101309498587651
   Aulacoseira islandica subsp. Helvetica O. Mull.9840134192271285
   Aulacoseira granulata (Ehr.)189115337414541702
   Aulacoseira italica (Ehr.)1333103175203198
   Hemidiscus cuneiformis 293521
   Cyclotella meneghiniana Kütz. ex Br. 721810867
   Cocconeis pediculus Ehr.4862489872
   Rhizosolenia longiseta 1211
   Rhizosolenia hebetata Bail.14
  Order II: Pennales
   Eunotia arcus Ehr.72372737
   Diatoma tenuis Bory11712111367
   Cymbella ventricosa Agardh3121242734
   Surirella debesi Turpin2427
   Surirella robusta var. splendida 21
   Surirella robusta var. armata 17
   Surirella linearis Turpin1947382731
   Synedra acus Ehr.2131
   Synedra ulna var. contracta Ehr.22182138
   Staurosirella leptostauron 14
   Asterionella formosa Hassall21207
   Gyrosigma scalproides Hassall19
   Gyrosigma attenuatum Hassall1613
   Gomphonema parvulum Ehr.2117243631
   Navicula lanceolata Bory98
   Navicula pupula Kütz. var. rectangularis Grun. Compr.32
   Navicula radiosa 192852
   Navicula margalithii 23573837
   Stauroneis anceps 27
   Nitzschiaacicularis Kütz.523733
   Nitzschia dissipata 182827
   Nitzschia intermedia 313134544241
   Nitzschia inconspicua 31323851
   Nitzschia closterium 3132
   Nitzschia gracilis 312944
   Pinnularia acrosphaeria (Breb.) var. minor Kütz.2736
   Pinnularia gibba 1731
   Pseudostaurosira brevistriata 11
   Amphora ovalis Kütz.4752
   Epithemia argus var. longicornis Grun.3919
   Epithemia sorex 47
   Rhopalodia operculata (Ehr.) Müller21
   Achnanthidium lanceolatum Kütz.2116
   Achnanthidium linearis Kütz.1227
Phylum: Chlorophyta
 Class: Chlorophyceae
  Order I: Chlorococcales
   Ankistrodesmus falcatus Ralfs var. mirabilis West f. longiseta Nygaard29
   Ankistrodesmus falcatus Ralfs var. spirilliformis West32
   Ankistrodesmus falcatus Ralfs18
   Ankistrodesmus falcatus Ralfs var. setiformis Nygaard f. brevis Nygaard22
   Ankistrodesmus gracilis Corda21
   Ankistrodesmus braianus 24
   Scenedesmus armatus Chodat19231113
   Scenedesmus perforates Meyen31
   Scenedesmus dispar f. canobe 2-cellulaire 11141222
   Scenedesmus quadricauda 111917
   Actinastrum Hantzschii Lagerheim11
   Kirchneriella sp. Schmidle7
   Tetrastrum stauroeniaeforme 16
   Tetrastrum heteracanthum f. epine par cellule 1413
   Selenastrum gracile Reinsch13
   Pediastrum simplex Meyen17
   Pediastrum duplex Meyen 17
   Pediastrum biradiatum var. longicornutum 16
   Pediastrum tetras Ralfs1711
   Quadrigula closterioides 11
   Crucigenia tetrapedia (Kirch.) West et G.S.1417
   Crucigenia minima Brunnthaler1416
  Order II: Zygnematales
   Spirogyra sp. Link37
   Closterium kutzingii f. sigmoides 2226
   Closterium jenneri Ralfs21
   Closterium parvulum Nag.32
   Staurastrum pingue Meyen ex Ralfs1918
   Staurastrum cyclocanthum var.  ubacanthum vue apicale 2113
   Staurodesmus dickiei var. maximus 14
   Cosmarium sp. Corda ex Ralfs13
   Cosmarium scottii 18
   Cosmarium trachypleurum 12
   Cosmarium sinostegos var. obstusius 7
Total species diversity ()242623634149
Total species abundance11697382009349033633767

Total abundanceRainfall

Water temperature0.7440.855*
Transparency−0.886* −0.755
Conductivity0.115 0.701
Reactive nitrate−0.533−0.375
Reactive phosphate0.247−0.319
Sulphate0.707 0.374
Peri. chlorophyll a −0.566−0.007

Correlation is significant at 0.05 level (2-tailed).
**Correlation is significant at 0.01 level (2-tailed).

Periphyton taxaDecemberJanuaryFebruaryMarch AprilMay

Total species diversity ()242623634149
Total abundance () cellsmL−111697382009349033633767
Shannon-Wiener index ()
Margalef’s index ()3.263.792.897.64.935.83

4. Discussion

The range value of the surface water temperature reported is notable for tropics. The highest water temperature observed in May could be a result of time of collection and heat capacity of water. The positive correlation that exists between rainfall and surface water temperature could explain the possible effect of precipitation on temperature. Nwankwo [28] reported that there are two main seasons in Nigeria: dry season (November–April) and wet season (May–October). The rainy season is ecologically more important in coastal waters and is bimodal in distribution. Floods caused by rainfall enrich the coastal environmental gradients (horizontal and vertical). With this seasonal pattern, it was observed that transparency, total dissolved solids, and total suspended solids increased with the onset of rainfall. The micronutrients concentration level increased as precipitation rate increased probably due to input from settlements and wetlands.

Odum [29] related pH levels to the amount of carbonate present in the water and often considered it an indicator of the aquatic chemical environment. The observed pH value (pH ≤ 6.6) falls within the range reported by Nwankwo and Akinsoji [30] for Epe Lagoon. The pH value could mainly be controlled by freshwater swamp exudates that regulate the acidity of the water body. Change in pH value has a profound effect on the conductivity level of the water. Furthermore, the high value of dissolved oxygen observed in January could be a result of combined photosynthetic activity of the microscopic plants, whereas the low value may be attributed to bacterial degradation of organic matter, which was observed at the onset of precipitation.

Hynes [31] reported that BOD values of 1-2 mg/L or less represent clean water, of 4–7 mg/L represent slightly polluted water, and of more than 8 mg/L represent severe pollution. Therefore based on the above criteria, the site was relatively clean except for December and March where levels of contamination were reported. The Shannon-Wiener index of diversity of 1–3 according to Wilh and Dorris [32] signifies moderately polluted water and above 3 signifies clean water situation. In this regard Shannon-Weiner index in December and March in periphyton community may point towards moderate pollution at this period.

However, the chlorophyll for periphyton community showed a rhythmic pattern with nutrient level mostly reactive nitrate. This may explain the importance of reactive nitrate to periphyton community. The periphyton abundance in the wet months differs significantly with that of dry months (; ). This could be a result of favourable conditions during this time that resulted in the multiplication of algal cell and additional input of pennate forms by the floods. The algal spectrum observed shows that diatoms were the dominant species in periphyton community.

Bowker and Denny [33] reported the limited growth of attached diatoms in the dry season and the rapid growth of macrophyte tissue. This may explain why more species were observed on macrophyte tissues in the wet months. Some of the algae that were common members of the plankton but were found in periphyton community were often trapped by the roots of the plant, like the centric diatoms. However, the centric diatoms found in the periphyton community were transit visitor caught up by the mesh formed of the water hyacinth roots.

The observations that diatoms dominate the periphyton community on water hyacinth confirm earlier reports [34, 35] that diatoms were more abundant in the algal spectrum of the Lagos Lagoon complex.

Round [36] observed the abundance of Eunotia sp. on Lemna roots whereas Bowker and Denny [33] reported the dominance of Achnanthes and Cocconeis sp. on the roots and leaves of Lemna, respectively. Cocconeis pediculus Ehr. and Achnanthidium sp. were only found in the periphyton community with Cocconeis occurring all through the months suggesting a strong coexistence. Cocconeis pediculus Ehr. occurred in a range of conditions from clean to moderately enriched to much enriched waters. Its presence and others (euglenoids; blue green algae; Nitzschia palea; Surirella sp.; Pinnularia sp.; Gomphonema parvulum; Mougeotia sp.; Spirogyra sp.; Trachelomonas affinis (Lemm.); T. ensifera Daday; T. gibberosa Playf.; Phormidium articulatum; Lyngbya intermedia; Cymbella ventricosa; Eunotia arcus; Surirella linearis; Asterionella formosa Hassall; N. acicularis; Amphora ovalis Kütz.; Ankistrodesmus falcatus; Scenedesmus armatus Chodat; and Closterium parvulum Nag.) may suggest pollution by organic materials.

The abundance of periphyton species on the water hyacinth may be given a second thought to enhance the aquaculture production in the area. A high species level for blue green algae and euglenoids in the periphyton community may reveal its suitability in monitoring environmental stress in coastal waters.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


Special thanks are due to the staff of Marine Biology Laboratory, University of Lagos, and Professor D. I. Nwankwo for the help throughout the study period.


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Copyright © 2015 A. I. Inyang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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