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Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3), 201-207
Asian-Australasian Journal of
Bioscience and Biotechnology
ISSN 2414-1283 (Print) 2414-6293 (Online)
www.ebupress.com/journal/aajbb
Article
Aquatic weeds diversity of Fatki River in Magura district, Bangladesh
Ripon Kumar Adhikary1*
, Md. Shahin Alam1
and Abdulla-Al-Asif1,2
1
Department of Fisheries and Marine Bioscience, Faculty of Biological Science and Technology, Jessore
University of Science and Technology, Jessore, 7408, Bangladesh
2
Department of Aquaculture, Faculty of Fisheries, Bangladesh Agricultural University, Mymensingh, 2202,
Bangladesh
*Corresponding author: Ripon Kumar Adhikary, Department of Fisheries and Marine Bioscience, Faculty of
Biological Science and Technology, Jessore University of Science and Technology, Jessore, 7408, Bangladesh.
Phone: +8801911969016; E-mail: rk.adhikary@just.edu.bd
Received: 28 November 2018/Accepted: 20 December 2018/ Published: 31 December 2018
Abstract: The study was conducted at Fatki River under Magura district to learn the aquatic weeds diversity
and abundance. This paper focused on species variation, number of species, water quality parameter and
identification of aquatic weeds. It was assessed by collecting samples from Chukinogor Ghat, Kechuadubi and
Arpara bazar during May to August, 2016. Aquatic weeds were abundant in rainy season and the semi-aquatic
weeds were available almost all the year round. According to this study, total 22 species belonging to 12 orders,
16 families and 21 genuses were found. Again, 46%, 28%, 26% of total aquatic weeds percentages identified
from the Chukinogor Ghat, Kechuadubi and Arpara bazar respectively. During this study period, nine species of
family Pontederiaceae, Convolvulaceae, Menyanthaceae, Asteraceae, Poaceae, Araceae, Amaranthaceae,
Polygonaceae were common in Chukinogor Ghat, Kechuadubi and Arpara bazar. Noticeable species– Lemna
minor, Marsilea quadrifolia, Ludwigia palustris, Aeschynomene aspera, Najas graminea, Hydrilla verticillata,
Najas guadalupensis, Utricularia inflate were only found in Chukinogor Ghat. This species are easily adapted
in large areas. On the other hands, two species were common in Chukinogor Ghat, Kechuadubi – Pistia
stratiotes and Equisetum hyemale. Prominent species of Arpara bazar were Cyperus rotundus and Xanthium
indicum. Total 11 species of aquatic weeds were mainly recognized from these Kechuadubi, while greatest
number was recorded of 20 species from Chukinogor Ghat and 12 species were have its place to Arpara bazar.
Management technique and water quality parameters were also studied during study period and the temperature
was recorded 29.0-30.00 ºC in Chukinogor Ghat, same as 28.0-320 ºC in Kechuadubi. Furthermore, 29.0-31.00
ºC temperature was found in Arpara bazar. DO levels were stable at ranged from7.0-7.5 ppm in Chukinogor
Ghat and 4.7-5.3 ppm was recorded in two experimental Kechuadubi 4.5-5.0 in Arpara bazar respectively. This
difference may arise due to the using of aerator in the Chukinogor Ghat same as decomposition, intensity of
light in Kechuadubi and Arpara bazar. Transparency was 28-32cm in Chukinogor Ghat, 36-44cm in
Kechuadubi, and 38-42 cm in Arpara bazar.
Keywords: aquatic macrophytes; diversity; abundance; water parameter; habitat
1. Introduction
The vegetation of haors, beels, lakes, and ponds are rich in aquatic weed and constitute very important resources
of food medicine for rural population (Khan and Halim, 2011). Aquatic weeds constitute an important role in
aquatic ecosystems and contribute to the general fitness and diversity of a healthy aquatic ecosystem (Flint and
Madsen, 1995) by acting as indicators for water quality and aiding in nutrient cycling (Carpenter and Lodge,
1986). From ecological point of view, aquatic plants stabilize bottom sediment, protect the shoreline from wave
erosion, and serve as feeding and nesting habitat for waterfowl. These plants provide food, shelter and
reproductive habitat or breeding ground for numerous fish and other aquatic animals (Lancer and Krake, 2002).
Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 202
There is an ecosystem imbalance between aquatic plants and other aquatic organisms when the plants invade the
system and grows excessively to a nuisance level. The excessive growth of aquatic weed restricts fishing,
swimming and recreational activities, causes foul taste and odour of drinking water supplies. It also leads to
stunting of fish populations and fish kill due to decomposition (Lansing, 2005). Aquatic weeds are used by man
as vegetables and fruits in the country and in some other countries. Some are used as human food and many
aquatic weeds are used for making compost fertilizer to use in River and agriculture land. Some fishes use
aquatic weed as food. Grass carp (Ctenopharyngodon idella) largely uses aquatic weed as food. Tilapia spp.
Cyprinus carpio use weeds as food to some extent. Many fishes eat soft parts of these plants in small quantity.
Moreover these plants harbour many insects, small invertebrates and periphyton which are used as fish food.
Rooted aquatic weeds prevent erosion of bottom soil. Many insects and invertebrates and some fishes used as
breeding places. Higher plants reduce turbidity. Turbidity producing silt and other particles settle on the
different parts of the plants body. They can be used carefully in well-managed and controlled conditions that can
increase fish production and as animal food and as fertilizer (Rahman, 1992). A very few researcher worked on
the percentage, composition, seasonal variation and occurrence of aquatic weed diversity from different water
body in Bangladesh. In Noakhali and Mymensingh region, any notable work had not done yet on these aquatic
weeds by any researcher. Research main motive was to identify various species of aquatic weeds and their
abundance and diversity. Knowledge on the aquatic weeds, we can understand the conditions of these different
water bodies and also how to improve these conditions which ultimately related to the fish production. So this
research was conducted in The River of Fatki which is originated from the River of Chitra and it’s located in
Kaligonj upazila under Jhenaidah district The River runs through the Upazila of Kaligonj, Magura Sadar, and
Shalikha within the district of Jhenaidah and Magura. This present study was carried out to identify the aquatic
weed species in different region of Fatki River and to determine the species variation of aquatic weeds in Arpara
bazar, Chukinogor Ghat and Kechuadubi of Fatki River under Magura district.
2. Materials and Methods
2.1. Sampling sites and periods
Samples were collected from four different locations at an interval of 1 km for 6 km which is adjacent to Fatki
River of Shalikha upazila of Magura (located at 23°15' and 23°41' north latitudes and in between 89°15' and
89°42' east longitudes at a mean elevation of 4 m above the sea level). Samples were taken from three places
Chukinogor Ghat, Kechuadubi and Arpara bazar of Fatki River under Magura district. The study was conducted
for a period of four (4) months from May 2016 to August 2016.
2.2. Sampling procedures and preservation
The samples were collected from selected areas of Fatki River. The samples were collected in plastic bags
aseptically following the methods and analysed the same day.
2.3. Sample collection
Some plastic bags are collected for sampling because samples should be protected. Samples were collected on
selected site basis from selected area in using different plastic bags for each sample. Samples were taken from
every sampling point during the study period. The samples were collected from water surface and below the
water surface in the morning hour between 8 to 10 AM. Samples were taken to the laboratory in appropriate
temperature (30-32)°C.
2.4. Taxonomic study and identification
Based on the photographs and sample observation taxonomy of the samples were determined following
references in Encyclopaedia of flora and fauna of Bangladesh, Aquatic angiosperms of Bangladesh. The
analysis was carried out within 3-4 hr. after collection. After capturing image, to complete the identification
process several books.
2.5. Data analysis
Data were processed and finally analyzed with Microsoft Excel 2007.
3. Results
3.1. Aquatic weed abundance
At the time of study, different types of species of weeds were found in the study area. The available weeds in
the selected area are given in Table 1 to Table 6 with their local names and scientific names.
Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 203
Table 1. Available species of aquatic weeds in Chukinogor Ghat-1.
Sl No. Local name Scientific name
1 Biskatali Polygonum coccineum
2 Tara lota Mikania cordata
3 Topapana Pistia stratiotes
4 Malancha Alternanthera philoxeroidis
5 Arail Leersia hexandra
6 Kalmilata Ipomoea aquatica
7 Spike rush Equisetum hyemale
8 Helencha Enhydra fluctuans
9 Kochu Colocasia esculenta
10 Kachuripana Eichhornia crassipes
11 Chand mala Nymphoides aquatica
Table 2. Available species of aquatic weeds in Chukinogor Ghat-2.
Sl No. Local name Scientific name
1 Chand mala Nymphoides aquatica
2 Helencha Enhydra fluctuans
3 Kachuripana Eichhornia crassipes
4 Kalmilata Ipomoea aquatica
5 Topapana Pistia stratiotes
6 Tara lota Mikania cordata
7 Kochu Colocasia esculenta
Table 3. Available species of aquatic weeds in Kochuadubi-1.
Sl No. Local name Scientific name
1 Chand mala Nymphoides aquatica
2 Shapla Nymphaea nouchali
3 Kalmilata Ipomoea aquatica
4 Arail Leersia hexandra
5 Spike rush Equisetum hyemale
6 Kachuripana Eichhornia crassipes
7 Najas grass Najas graminea
8 Topapana Pistia stratiotes
9 Malancha Alternanthera philoxeroidis
10 Kochu Colocasia esculenta
11 Tara lota Mikania cordata
12 Biskatali Polygonum coccineum
13 Goromi Najas guadalupensis
14 Kormota Ludwigia palustris
15 Shushnipata Marsilea quadrifolia
16 Helencha Enhydra fluctuans
17 Khudipana Lemna minor
18 Hydrilla grass Hydrilla verticillata
19 Hobon Utricularia inflata
Table 4. Available species of aquatic weeds in Kochuadubi-2.
Sl No. Local name Scientific name
1 Spike rush Equisetum hyemale
2 Shapla Nymphaea nouchali
3 Arail Leersia hexandra
4 Kachuripana Eichhornia crassipes
5 Chand mala Nymphodies aquatica
6 Hobon Utricularia inflate
7 Helencha Enhydra fluctuans
8 Malancha Alternanthera philoxeroidis
9 Tara lota Mikania cordata
10 Vatshola Aeschynomene aspera
11 Biskatali Polygonum coccineum
12 Goromi Najas guadalupensis
13 Topapana Pistia stratiotes
Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 204
Table 5. Available species of aquatic weeds in Arpara bazar- 1.
Sl No. Local name Scientific name
1 Biskatali Polygonum coccineum
2 Helencha Enhydra fluctuans
3 Chand mala Nymphoides aquatica
4 Kalmilata Ipomoea aquatica
5 Kochu Colocasia esculenta
6 Tara lota Mikania cordata
7 Shapla Nymphaea nouchali
8 Arail Leersia hexandra
9 Kachuripana Eichhornia crassipes
Table 6. Available species of aquatic weeds in Arpara bazar-2.
Sl No. Local name Scientific name
1 Gagra Xanthium indicum
2 Helencha Enhydra fluctuans
3 Chand mala Nymphoides aquatica
4 Kalmilata Ipomaea aquatic
5 Kochu Colocasia esculenta
6 Tara lota Mikania cordata
7 Shapla Nymphaea nouchali
8 Arail Leersia hexandra
9 Biskatali Polygonum coccineum
10 Malancha Alternanthera philoxeroidis
11 Mutha Cyperus rotundus
12 Kachuripana Eichhornia crassipes
3.2. Taxonomic status
The taxonomic details of the aquatic weeds are enormous variant in the study area. The taxonomic formation is
shown in Table 7. The number of the species which found in the study area is also shown in Table 8.
Table 7. Taxonomic status of the aquatic weeds recorded from selected sites.
Sl No. Order Family Genus Species Habitat Type
01 Commelinales Pontederiaceae Eichhornia E. crassipes CG, KD, AB
02 Alismatales Araceae Pistia P. stratiote CG, KD
Colocasia C. esculenta CG, KD, AB
Lemna Lemna minor KD
Hydrocharitaceae Najas N. guadalupensis
N. graminea
KD
KD
Hydrilla H. verticillata KD
03 Solanales Convolvulaceae Ipomoea I. aquatic CG, KD. AB
04 Poales Poaceae Leersia L. hexandra CG, KD. AB
Cyperaceae Cyperus C. rotundus AB
05 Asterales Asteraceae Enhydra E. fluctuans CG, KD, AB
Mikania M. cordata CG, KD. AB
Xanthium X. indicum AB
Menyanthaceae Nymphoides N. aquatic CG, KD, AB
06 Nymphaeales Nymphaeaceae Nymphaea N. nouchali KD, AB
07 Lamiales Lentibulariaceae Utricularia U. inflate KD
08 Caryophyllales Amaranthaceae Alternanthera A. philoxeroides CG, KD, AB
Polygonaceae Polygonum P. coccineum CG, KD, AB
09 Equisetales Equisetaceae Equisetum E. hyemale CG, KD
10 Myrtales Onagraceae Ludwigia L. palustris KD
11 Salviniales Marsileaceae Marsilea M. quadrifolia KD
12 Fabales Fabaceae Aeschynomene A. aspera KD
**CG= Chukinogor Ghat; KD= Kechuadubi; AB= Arpara bazar
Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 205
Table 8. Number of Order, Family, Genus, Species in different habitat location.
Place No. of Order No. of Family No. of Genus No. of Species
Chukinogor Ghat 7 9 11 11
Kechuadubi 12 15 19 20
Arpara bazar 6 9 12 12
3.3. Comparison of aquatic weed in different water bodies
Among the sampling points there are two types of aquatic weed were found. Highest amount of species
variation found in the Kechuadubi. On the other hand, Chukinogor and Arpara bazar showed the lowest amount
of species (Figure 1).
Figure 1. Comparison of aquatic weed in different water bodies.
3.5. Water quality parameters observed in the different water bodies.
Water temperatures were found to be stable always at range of 29-300
C and was found within suitable range for
fish production. During the study period, DO levels were found high value in Chukinogor Ghat. The lowest
values are found in roadside canals. Transparency was recorded high number at Kechuadubi and lowest at
Chukinogor Ghat. The water quality parameters have been shown in Table 9.
Table 9. Water quality parameters in different water bodies.
Parameters Chukinogor Ghat Kechuadubi Arpara bazar
DO mg/l 7.25±0.25 5±0.3 4.75±0.25
Salinity (ppt) 0 0 0
Temperature (0
c) 29±1 30±2 30±1
Transparency(cm) 30±2 40±4 40±2
4. Discussion
Aquatic weeds are classified according to various habitats which form their eco-environment and become
conducive for their growth; reproduction and According to this study, a total of 22 species of 16 families, 12
orders and 21 genes were found. Among them some was highly dominated and some are only found in single
selected site. During this study period, nine species- Eichhornia crassipes, Ipomoea aquatica, Nymphiodes
aquatica, Enhydra fluctuans, Leersia hexandra, Mikania cordata, Colocasia esculenta, Polygonum coccineum,
Alternanthera philoxeroydis were common in Chukinogor Ghat, Kechuadubi, and Arpara bazar. But their
abundance is significantly different. Rahman (2013) recorded the total angiosperm weed species under 123
genera and 50 families were recorded in that study. Out of the total number of species 98 were frequent, 41 were
abundant, 15 were rare and 1 was very rare species. Islam et al. (2017) found that, a total of 39 weed and aquatic
species were identified in the Bangladesh Agricultural University campus. Kaisar et al. (2016) recognised 22
aquatic weed species in Noakhali sadar area, Bangladesh. Billah et al. (2018) found 37 marine species in Saint
Martin Island. In this study, eight species were only found in floodplain – Lemma minor, Marsilea quadrifolia,
Ludwigia palustris, Aeschynomene aspera, Najas graminea, Hydrilla verticillata, Najas guadalupensis, and
Utricularia inflata. This species are easily adapted in large areas. On the other hands, two species were common
in Chukinogor Ghat, Kechuadubi – Pistia stratiotes and Equisetum hyemale. Cyperus rotundus and Xanthium
indicum were the two species which only found in Arpara bazar. Chowdhury and Ahmed (2012) included a total
of 29 genera belonging to 24 families of aquatic macrophysics were recorded. Among these, 25species were
recorded from the freshwater aquatic ecosystems, 4 species from both the shrimp Chukinogor Ghat sand
0
5
10
15
20
25
30
35
40
45
50
Chukinogor Ghat Kechuadubi Arpara Bazar
Percentage
Sampling site
Chukinogor Ghat
Kechuadubi
Arpara Bazar
Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 206
freshwater aquatic ecosystems and only one from the shrimp Chukinogor Ghat. Regarding this study,
Chukinogor Ghat had the lowest number of species because of proper maintenance through pollution. Jayan and
Sathyanathan (2012) recorded the major aquatic weeds found in Kerala include Salvinia spp., Eichhornia
crassipes, Pistia stratiotes, Alternanthera spp., Azolla, common duckweed, and Hydrilla verticillata. In present
study, Kechuadubi has the greatest amounts of aquatic weed variety and among all 22 species around 20 species
were identified from this Kechuadubi. Shallow waters were found to be ideal habitat for most of the aquatic
weed species due to the highest amount of light penetration. As the Kechuadubi had the high diversity of aquatic
weed because of it was not filled with larger aquatic weed like as water spinach, water hyacinth, Hydrilla grass
etc. The network of drainage channels, are so badly infested in Arpara bazar which was responsible for larger
amounts of aquatic weeds. Turbid water which causes low light penetration limits the aquatic weeds. Aquatic
weeds such as duckweeds, azolla etc. amount was so high for that species variation was low in the Arpara bazar.
Uka et al. (2009) detected eight aquatic plants have been incriminated as weeds. From the current study, the
most prevalent of these weeds are water hyacinth and cattail plants. Aquatic weeds cause taste and odours
problems and also increase biological oxygen demand because of organic loading. They increase the organic
matter content of water which affects the strength of the concrete structures when used as curing and mixing
water. Water temperature is a pre-requisite for increasing the weed density. In the present study, temperature
and pH value was recorded 29.0-30.00
C and 7.5-7.8 in Chukinogor Ghat, 28.0-320
C and 7.9-8.2 in Kechuadubi,
29.0-310
C and 8.3-8.7 in Arpara bazar respectively. Chowdhury et al., (2007b) recorded the temperature yearly
ranged from 18.50
C in December to 33.720
C in August and pH value is 7.12-8.68 at Borobila beel in Rangpur
district. Eloff and Vander (1981) reported that temperature 270
C to 290
C and the pH value 6.5 to 10.5 in their
study. Raju et al. (2018) also performed such similar study in plankton population and the water parameters
were also relatively similar. During the study period, DO levels were stable at ranged from7-7.5 ppm in
Chukinogor Ghat and 4.7-5.3 ppm was recorded in two experimental Kechuadubi, 4.5-5.0 in Arpara bazar
respectively. This difference may arise due to the using of aerator in the Chukinogor Ghat and decomposition in
Kechuadubi and Arpara bazar. According to this study, transparency was 28-32cm in Chukinogor Ghat, 36-44
cm in Kechuadubi, and 38-42 cm in Arpara bazar. But this wide range of variation in pond due to the using only
hormonal feed and not using other feed and fertilizer. During this study there was no salinity found in the study
area, which hampers the growth of aquatic weeds. High levels of salinity in wastewater can limit the growth of
water hyacinth and other aquatic macrophysics (Sooknah and Wilkie, 2004; Chowdhury et al., 2007a).
Chowdhury and Ahmed (2012) showed that the physicochemical conditions of both the habitats indicate that
very poor number of macrophysics can grow in the shrimp due to high salinity of water and soil.
5. Conclusions
In conclusion, Macrophytes are an important component of the aquatic ecosystem and broad changes in the
abundance of individual species and community composition provide valuable information on how and why an
ecosystem might be changing. Aquatic weed concentrations are highly responsive to nutrient levels,
temperatures, transparency, DO level and also the management option. So density of weeds varies from water
bodies to water bodies on the basis of water quality parameter etc. Study of diversity of aquatic weeds is
important for evaluating the water quality and also the fish production.
Conflict of interest
None to declare.
References
Billah MM, MA Kader, SS Mahmud, AA Asif and AAM Siddiqui, 2018. Diversity and distribution of seaweeds
in Saint Martin Island, Bangladesh. Int. J. Fish. Aqua. Stud., 6: 166-169.
Carpenter SR and DM Lodge, 1986. Effects of submersed macrophytes on ecosystem processes. Aquatic
Botany, 26: 341-370.
Chowdhury A and R Ahmed, 2012. Water, sediment and macrophyte quality of some shrimp culture ponds and
freshwater ecosystems of Koyra. Bangladesh J. Bot., 41: 35-41.
Chowdhury AMS, MA Rahman, MM Rahman, ASM Mohiuddin and MB Zaman, 2007a. Nature and the extent
of industrial pollution in river water around Dhaka city. Bangladesh J. Env. Sci., 13: 46-49.
Chowdhury MMR, MRK Mondol and C Sarker, 2007b. Seasonal variation of plankton population of
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Eloff JN and AJ Vander, 1981. Toxicology studies on Microcystis. In: The water environment algal toxin and
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Aquatic weeds diversity of Fatki River in Magura district, Bangladesh

  • 1. Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3), 201-207 Asian-Australasian Journal of Bioscience and Biotechnology ISSN 2414-1283 (Print) 2414-6293 (Online) www.ebupress.com/journal/aajbb Article Aquatic weeds diversity of Fatki River in Magura district, Bangladesh Ripon Kumar Adhikary1* , Md. Shahin Alam1 and Abdulla-Al-Asif1,2 1 Department of Fisheries and Marine Bioscience, Faculty of Biological Science and Technology, Jessore University of Science and Technology, Jessore, 7408, Bangladesh 2 Department of Aquaculture, Faculty of Fisheries, Bangladesh Agricultural University, Mymensingh, 2202, Bangladesh *Corresponding author: Ripon Kumar Adhikary, Department of Fisheries and Marine Bioscience, Faculty of Biological Science and Technology, Jessore University of Science and Technology, Jessore, 7408, Bangladesh. Phone: +8801911969016; E-mail: rk.adhikary@just.edu.bd Received: 28 November 2018/Accepted: 20 December 2018/ Published: 31 December 2018 Abstract: The study was conducted at Fatki River under Magura district to learn the aquatic weeds diversity and abundance. This paper focused on species variation, number of species, water quality parameter and identification of aquatic weeds. It was assessed by collecting samples from Chukinogor Ghat, Kechuadubi and Arpara bazar during May to August, 2016. Aquatic weeds were abundant in rainy season and the semi-aquatic weeds were available almost all the year round. According to this study, total 22 species belonging to 12 orders, 16 families and 21 genuses were found. Again, 46%, 28%, 26% of total aquatic weeds percentages identified from the Chukinogor Ghat, Kechuadubi and Arpara bazar respectively. During this study period, nine species of family Pontederiaceae, Convolvulaceae, Menyanthaceae, Asteraceae, Poaceae, Araceae, Amaranthaceae, Polygonaceae were common in Chukinogor Ghat, Kechuadubi and Arpara bazar. Noticeable species– Lemna minor, Marsilea quadrifolia, Ludwigia palustris, Aeschynomene aspera, Najas graminea, Hydrilla verticillata, Najas guadalupensis, Utricularia inflate were only found in Chukinogor Ghat. This species are easily adapted in large areas. On the other hands, two species were common in Chukinogor Ghat, Kechuadubi – Pistia stratiotes and Equisetum hyemale. Prominent species of Arpara bazar were Cyperus rotundus and Xanthium indicum. Total 11 species of aquatic weeds were mainly recognized from these Kechuadubi, while greatest number was recorded of 20 species from Chukinogor Ghat and 12 species were have its place to Arpara bazar. Management technique and water quality parameters were also studied during study period and the temperature was recorded 29.0-30.00 ºC in Chukinogor Ghat, same as 28.0-320 ºC in Kechuadubi. Furthermore, 29.0-31.00 ºC temperature was found in Arpara bazar. DO levels were stable at ranged from7.0-7.5 ppm in Chukinogor Ghat and 4.7-5.3 ppm was recorded in two experimental Kechuadubi 4.5-5.0 in Arpara bazar respectively. This difference may arise due to the using of aerator in the Chukinogor Ghat same as decomposition, intensity of light in Kechuadubi and Arpara bazar. Transparency was 28-32cm in Chukinogor Ghat, 36-44cm in Kechuadubi, and 38-42 cm in Arpara bazar. Keywords: aquatic macrophytes; diversity; abundance; water parameter; habitat 1. Introduction The vegetation of haors, beels, lakes, and ponds are rich in aquatic weed and constitute very important resources of food medicine for rural population (Khan and Halim, 2011). Aquatic weeds constitute an important role in aquatic ecosystems and contribute to the general fitness and diversity of a healthy aquatic ecosystem (Flint and Madsen, 1995) by acting as indicators for water quality and aiding in nutrient cycling (Carpenter and Lodge, 1986). From ecological point of view, aquatic plants stabilize bottom sediment, protect the shoreline from wave erosion, and serve as feeding and nesting habitat for waterfowl. These plants provide food, shelter and reproductive habitat or breeding ground for numerous fish and other aquatic animals (Lancer and Krake, 2002).
  • 2. Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 202 There is an ecosystem imbalance between aquatic plants and other aquatic organisms when the plants invade the system and grows excessively to a nuisance level. The excessive growth of aquatic weed restricts fishing, swimming and recreational activities, causes foul taste and odour of drinking water supplies. It also leads to stunting of fish populations and fish kill due to decomposition (Lansing, 2005). Aquatic weeds are used by man as vegetables and fruits in the country and in some other countries. Some are used as human food and many aquatic weeds are used for making compost fertilizer to use in River and agriculture land. Some fishes use aquatic weed as food. Grass carp (Ctenopharyngodon idella) largely uses aquatic weed as food. Tilapia spp. Cyprinus carpio use weeds as food to some extent. Many fishes eat soft parts of these plants in small quantity. Moreover these plants harbour many insects, small invertebrates and periphyton which are used as fish food. Rooted aquatic weeds prevent erosion of bottom soil. Many insects and invertebrates and some fishes used as breeding places. Higher plants reduce turbidity. Turbidity producing silt and other particles settle on the different parts of the plants body. They can be used carefully in well-managed and controlled conditions that can increase fish production and as animal food and as fertilizer (Rahman, 1992). A very few researcher worked on the percentage, composition, seasonal variation and occurrence of aquatic weed diversity from different water body in Bangladesh. In Noakhali and Mymensingh region, any notable work had not done yet on these aquatic weeds by any researcher. Research main motive was to identify various species of aquatic weeds and their abundance and diversity. Knowledge on the aquatic weeds, we can understand the conditions of these different water bodies and also how to improve these conditions which ultimately related to the fish production. So this research was conducted in The River of Fatki which is originated from the River of Chitra and it’s located in Kaligonj upazila under Jhenaidah district The River runs through the Upazila of Kaligonj, Magura Sadar, and Shalikha within the district of Jhenaidah and Magura. This present study was carried out to identify the aquatic weed species in different region of Fatki River and to determine the species variation of aquatic weeds in Arpara bazar, Chukinogor Ghat and Kechuadubi of Fatki River under Magura district. 2. Materials and Methods 2.1. Sampling sites and periods Samples were collected from four different locations at an interval of 1 km for 6 km which is adjacent to Fatki River of Shalikha upazila of Magura (located at 23°15' and 23°41' north latitudes and in between 89°15' and 89°42' east longitudes at a mean elevation of 4 m above the sea level). Samples were taken from three places Chukinogor Ghat, Kechuadubi and Arpara bazar of Fatki River under Magura district. The study was conducted for a period of four (4) months from May 2016 to August 2016. 2.2. Sampling procedures and preservation The samples were collected from selected areas of Fatki River. The samples were collected in plastic bags aseptically following the methods and analysed the same day. 2.3. Sample collection Some plastic bags are collected for sampling because samples should be protected. Samples were collected on selected site basis from selected area in using different plastic bags for each sample. Samples were taken from every sampling point during the study period. The samples were collected from water surface and below the water surface in the morning hour between 8 to 10 AM. Samples were taken to the laboratory in appropriate temperature (30-32)°C. 2.4. Taxonomic study and identification Based on the photographs and sample observation taxonomy of the samples were determined following references in Encyclopaedia of flora and fauna of Bangladesh, Aquatic angiosperms of Bangladesh. The analysis was carried out within 3-4 hr. after collection. After capturing image, to complete the identification process several books. 2.5. Data analysis Data were processed and finally analyzed with Microsoft Excel 2007. 3. Results 3.1. Aquatic weed abundance At the time of study, different types of species of weeds were found in the study area. The available weeds in the selected area are given in Table 1 to Table 6 with their local names and scientific names.
  • 3. Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 203 Table 1. Available species of aquatic weeds in Chukinogor Ghat-1. Sl No. Local name Scientific name 1 Biskatali Polygonum coccineum 2 Tara lota Mikania cordata 3 Topapana Pistia stratiotes 4 Malancha Alternanthera philoxeroidis 5 Arail Leersia hexandra 6 Kalmilata Ipomoea aquatica 7 Spike rush Equisetum hyemale 8 Helencha Enhydra fluctuans 9 Kochu Colocasia esculenta 10 Kachuripana Eichhornia crassipes 11 Chand mala Nymphoides aquatica Table 2. Available species of aquatic weeds in Chukinogor Ghat-2. Sl No. Local name Scientific name 1 Chand mala Nymphoides aquatica 2 Helencha Enhydra fluctuans 3 Kachuripana Eichhornia crassipes 4 Kalmilata Ipomoea aquatica 5 Topapana Pistia stratiotes 6 Tara lota Mikania cordata 7 Kochu Colocasia esculenta Table 3. Available species of aquatic weeds in Kochuadubi-1. Sl No. Local name Scientific name 1 Chand mala Nymphoides aquatica 2 Shapla Nymphaea nouchali 3 Kalmilata Ipomoea aquatica 4 Arail Leersia hexandra 5 Spike rush Equisetum hyemale 6 Kachuripana Eichhornia crassipes 7 Najas grass Najas graminea 8 Topapana Pistia stratiotes 9 Malancha Alternanthera philoxeroidis 10 Kochu Colocasia esculenta 11 Tara lota Mikania cordata 12 Biskatali Polygonum coccineum 13 Goromi Najas guadalupensis 14 Kormota Ludwigia palustris 15 Shushnipata Marsilea quadrifolia 16 Helencha Enhydra fluctuans 17 Khudipana Lemna minor 18 Hydrilla grass Hydrilla verticillata 19 Hobon Utricularia inflata Table 4. Available species of aquatic weeds in Kochuadubi-2. Sl No. Local name Scientific name 1 Spike rush Equisetum hyemale 2 Shapla Nymphaea nouchali 3 Arail Leersia hexandra 4 Kachuripana Eichhornia crassipes 5 Chand mala Nymphodies aquatica 6 Hobon Utricularia inflate 7 Helencha Enhydra fluctuans 8 Malancha Alternanthera philoxeroidis 9 Tara lota Mikania cordata 10 Vatshola Aeschynomene aspera 11 Biskatali Polygonum coccineum 12 Goromi Najas guadalupensis 13 Topapana Pistia stratiotes
  • 4. Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 204 Table 5. Available species of aquatic weeds in Arpara bazar- 1. Sl No. Local name Scientific name 1 Biskatali Polygonum coccineum 2 Helencha Enhydra fluctuans 3 Chand mala Nymphoides aquatica 4 Kalmilata Ipomoea aquatica 5 Kochu Colocasia esculenta 6 Tara lota Mikania cordata 7 Shapla Nymphaea nouchali 8 Arail Leersia hexandra 9 Kachuripana Eichhornia crassipes Table 6. Available species of aquatic weeds in Arpara bazar-2. Sl No. Local name Scientific name 1 Gagra Xanthium indicum 2 Helencha Enhydra fluctuans 3 Chand mala Nymphoides aquatica 4 Kalmilata Ipomaea aquatic 5 Kochu Colocasia esculenta 6 Tara lota Mikania cordata 7 Shapla Nymphaea nouchali 8 Arail Leersia hexandra 9 Biskatali Polygonum coccineum 10 Malancha Alternanthera philoxeroidis 11 Mutha Cyperus rotundus 12 Kachuripana Eichhornia crassipes 3.2. Taxonomic status The taxonomic details of the aquatic weeds are enormous variant in the study area. The taxonomic formation is shown in Table 7. The number of the species which found in the study area is also shown in Table 8. Table 7. Taxonomic status of the aquatic weeds recorded from selected sites. Sl No. Order Family Genus Species Habitat Type 01 Commelinales Pontederiaceae Eichhornia E. crassipes CG, KD, AB 02 Alismatales Araceae Pistia P. stratiote CG, KD Colocasia C. esculenta CG, KD, AB Lemna Lemna minor KD Hydrocharitaceae Najas N. guadalupensis N. graminea KD KD Hydrilla H. verticillata KD 03 Solanales Convolvulaceae Ipomoea I. aquatic CG, KD. AB 04 Poales Poaceae Leersia L. hexandra CG, KD. AB Cyperaceae Cyperus C. rotundus AB 05 Asterales Asteraceae Enhydra E. fluctuans CG, KD, AB Mikania M. cordata CG, KD. AB Xanthium X. indicum AB Menyanthaceae Nymphoides N. aquatic CG, KD, AB 06 Nymphaeales Nymphaeaceae Nymphaea N. nouchali KD, AB 07 Lamiales Lentibulariaceae Utricularia U. inflate KD 08 Caryophyllales Amaranthaceae Alternanthera A. philoxeroides CG, KD, AB Polygonaceae Polygonum P. coccineum CG, KD, AB 09 Equisetales Equisetaceae Equisetum E. hyemale CG, KD 10 Myrtales Onagraceae Ludwigia L. palustris KD 11 Salviniales Marsileaceae Marsilea M. quadrifolia KD 12 Fabales Fabaceae Aeschynomene A. aspera KD **CG= Chukinogor Ghat; KD= Kechuadubi; AB= Arpara bazar
  • 5. Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 205 Table 8. Number of Order, Family, Genus, Species in different habitat location. Place No. of Order No. of Family No. of Genus No. of Species Chukinogor Ghat 7 9 11 11 Kechuadubi 12 15 19 20 Arpara bazar 6 9 12 12 3.3. Comparison of aquatic weed in different water bodies Among the sampling points there are two types of aquatic weed were found. Highest amount of species variation found in the Kechuadubi. On the other hand, Chukinogor and Arpara bazar showed the lowest amount of species (Figure 1). Figure 1. Comparison of aquatic weed in different water bodies. 3.5. Water quality parameters observed in the different water bodies. Water temperatures were found to be stable always at range of 29-300 C and was found within suitable range for fish production. During the study period, DO levels were found high value in Chukinogor Ghat. The lowest values are found in roadside canals. Transparency was recorded high number at Kechuadubi and lowest at Chukinogor Ghat. The water quality parameters have been shown in Table 9. Table 9. Water quality parameters in different water bodies. Parameters Chukinogor Ghat Kechuadubi Arpara bazar DO mg/l 7.25±0.25 5±0.3 4.75±0.25 Salinity (ppt) 0 0 0 Temperature (0 c) 29±1 30±2 30±1 Transparency(cm) 30±2 40±4 40±2 4. Discussion Aquatic weeds are classified according to various habitats which form their eco-environment and become conducive for their growth; reproduction and According to this study, a total of 22 species of 16 families, 12 orders and 21 genes were found. Among them some was highly dominated and some are only found in single selected site. During this study period, nine species- Eichhornia crassipes, Ipomoea aquatica, Nymphiodes aquatica, Enhydra fluctuans, Leersia hexandra, Mikania cordata, Colocasia esculenta, Polygonum coccineum, Alternanthera philoxeroydis were common in Chukinogor Ghat, Kechuadubi, and Arpara bazar. But their abundance is significantly different. Rahman (2013) recorded the total angiosperm weed species under 123 genera and 50 families were recorded in that study. Out of the total number of species 98 were frequent, 41 were abundant, 15 were rare and 1 was very rare species. Islam et al. (2017) found that, a total of 39 weed and aquatic species were identified in the Bangladesh Agricultural University campus. Kaisar et al. (2016) recognised 22 aquatic weed species in Noakhali sadar area, Bangladesh. Billah et al. (2018) found 37 marine species in Saint Martin Island. In this study, eight species were only found in floodplain – Lemma minor, Marsilea quadrifolia, Ludwigia palustris, Aeschynomene aspera, Najas graminea, Hydrilla verticillata, Najas guadalupensis, and Utricularia inflata. This species are easily adapted in large areas. On the other hands, two species were common in Chukinogor Ghat, Kechuadubi – Pistia stratiotes and Equisetum hyemale. Cyperus rotundus and Xanthium indicum were the two species which only found in Arpara bazar. Chowdhury and Ahmed (2012) included a total of 29 genera belonging to 24 families of aquatic macrophysics were recorded. Among these, 25species were recorded from the freshwater aquatic ecosystems, 4 species from both the shrimp Chukinogor Ghat sand 0 5 10 15 20 25 30 35 40 45 50 Chukinogor Ghat Kechuadubi Arpara Bazar Percentage Sampling site Chukinogor Ghat Kechuadubi Arpara Bazar
  • 6. Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 206 freshwater aquatic ecosystems and only one from the shrimp Chukinogor Ghat. Regarding this study, Chukinogor Ghat had the lowest number of species because of proper maintenance through pollution. Jayan and Sathyanathan (2012) recorded the major aquatic weeds found in Kerala include Salvinia spp., Eichhornia crassipes, Pistia stratiotes, Alternanthera spp., Azolla, common duckweed, and Hydrilla verticillata. In present study, Kechuadubi has the greatest amounts of aquatic weed variety and among all 22 species around 20 species were identified from this Kechuadubi. Shallow waters were found to be ideal habitat for most of the aquatic weed species due to the highest amount of light penetration. As the Kechuadubi had the high diversity of aquatic weed because of it was not filled with larger aquatic weed like as water spinach, water hyacinth, Hydrilla grass etc. The network of drainage channels, are so badly infested in Arpara bazar which was responsible for larger amounts of aquatic weeds. Turbid water which causes low light penetration limits the aquatic weeds. Aquatic weeds such as duckweeds, azolla etc. amount was so high for that species variation was low in the Arpara bazar. Uka et al. (2009) detected eight aquatic plants have been incriminated as weeds. From the current study, the most prevalent of these weeds are water hyacinth and cattail plants. Aquatic weeds cause taste and odours problems and also increase biological oxygen demand because of organic loading. They increase the organic matter content of water which affects the strength of the concrete structures when used as curing and mixing water. Water temperature is a pre-requisite for increasing the weed density. In the present study, temperature and pH value was recorded 29.0-30.00 C and 7.5-7.8 in Chukinogor Ghat, 28.0-320 C and 7.9-8.2 in Kechuadubi, 29.0-310 C and 8.3-8.7 in Arpara bazar respectively. Chowdhury et al., (2007b) recorded the temperature yearly ranged from 18.50 C in December to 33.720 C in August and pH value is 7.12-8.68 at Borobila beel in Rangpur district. Eloff and Vander (1981) reported that temperature 270 C to 290 C and the pH value 6.5 to 10.5 in their study. Raju et al. (2018) also performed such similar study in plankton population and the water parameters were also relatively similar. During the study period, DO levels were stable at ranged from7-7.5 ppm in Chukinogor Ghat and 4.7-5.3 ppm was recorded in two experimental Kechuadubi, 4.5-5.0 in Arpara bazar respectively. This difference may arise due to the using of aerator in the Chukinogor Ghat and decomposition in Kechuadubi and Arpara bazar. According to this study, transparency was 28-32cm in Chukinogor Ghat, 36-44 cm in Kechuadubi, and 38-42 cm in Arpara bazar. But this wide range of variation in pond due to the using only hormonal feed and not using other feed and fertilizer. During this study there was no salinity found in the study area, which hampers the growth of aquatic weeds. High levels of salinity in wastewater can limit the growth of water hyacinth and other aquatic macrophysics (Sooknah and Wilkie, 2004; Chowdhury et al., 2007a). Chowdhury and Ahmed (2012) showed that the physicochemical conditions of both the habitats indicate that very poor number of macrophysics can grow in the shrimp due to high salinity of water and soil. 5. Conclusions In conclusion, Macrophytes are an important component of the aquatic ecosystem and broad changes in the abundance of individual species and community composition provide valuable information on how and why an ecosystem might be changing. Aquatic weed concentrations are highly responsive to nutrient levels, temperatures, transparency, DO level and also the management option. So density of weeds varies from water bodies to water bodies on the basis of water quality parameter etc. Study of diversity of aquatic weeds is important for evaluating the water quality and also the fish production. Conflict of interest None to declare. References Billah MM, MA Kader, SS Mahmud, AA Asif and AAM Siddiqui, 2018. Diversity and distribution of seaweeds in Saint Martin Island, Bangladesh. Int. J. Fish. Aqua. Stud., 6: 166-169. Carpenter SR and DM Lodge, 1986. Effects of submersed macrophytes on ecosystem processes. Aquatic Botany, 26: 341-370. Chowdhury A and R Ahmed, 2012. Water, sediment and macrophyte quality of some shrimp culture ponds and freshwater ecosystems of Koyra. Bangladesh J. Bot., 41: 35-41. Chowdhury AMS, MA Rahman, MM Rahman, ASM Mohiuddin and MB Zaman, 2007a. Nature and the extent of industrial pollution in river water around Dhaka city. Bangladesh J. Env. Sci., 13: 46-49. Chowdhury MMR, MRK Mondol and C Sarker, 2007b. Seasonal variation of plankton population of Borobilabeel in Rangpur district. Journal of zoology, 26: 49-54. Eloff JN and AJ Vander, 1981. Toxicology studies on Microcystis. In: The water environment algal toxin and health. Carmichael, W. W (eds.). Plenum Press, New York. pp. 343-364.
  • 7. Asian Australas. J. Biosci. Biotechnol. 2018, 3 (3) 207 Flint NA and JD Madsen, 1995. The effect of temperature and day length on the germination of Potamogeton nodosus tubers. J. Freshwat. Ecol., 10:125-128. Islam MD, SM Rahmatullah, M Ahmed, AA Asif, A Satter, B Sarker, A Hossain and S Mojumder, 2017. Aquatic weeds diversity of Bangladesh Agricultural University Campus, Mymensingh, Bangladesh. Asian Australas. J. Biosci. Biotechnol., 2: 181-192. Jayan PR and N Sathyanathan, 2012. Aquatic weed classification, environmental effects and the management technologies form its effective control in Kerala, India. Int. J. Agri. Biol. Eng., 5: 76–91. Kaisar MI, RK Adhikary, M Dutta and S Bhowmik, 2016. Diversity of aquatic weeds at Noakhali sadar in Bangladesh. Am. J. Sci. Ind. Res., 7: 117-128. Khan MS and M Halim, 2011. Aquatic angiosperms of Bangladesh. Bangladesh National Herbarium, Dhaka. Lancer L and K Krake, 2002. Aquatic weed and their management. International Commission on Irrigation and Drainage. pp. 50-65. Lansing MI, 2005. Aquatic plant management: Best management practices in support of fish and wildlife habitat. Ecosystem Restoration Foundation, pp.1-78. Rahman AHM, 2013. A Checklist of Common Angiosperm Weeds of Rajshahi District, Bangladesh. Int. J. Agri. Soil Sci., 1: 1-6. Rahman MS, 1992. Water Quality Management in Aquaculture. BRAC Prokashana, Mohakhali, Dhaka, Bangladesh, pp. 84-90. Raju RH, MA Samad, AA Asif, MM Billah and MA Ali, 2018.Variation in the plankton abundance, biomass and diversity of municipal pond and Bukvorabaor at Jashore district, Bangladesh. Res. Rev. J. Bioinfo., 5: 1– 14. Sooknah R and A Wilkie, 2004. Nutrient removal by floating aquatic macrophytes cultured anaerobically digested flushed dairy manure wastewater. Ecological Engineering, 22: 27-42. Uka UN, HA Mohammed and SI Ovie, 2009. Current diversity of aquatic macrophytes in Nigerian freshwater ecosystem. Brazilian J. S. Tech., 13: 9-15.