INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1778
www.rsisinternational.org
Investigation of Submerged Aquatic Macrophytes in Chhatrapati
Sambhajinagar District of Maharashtra
Sangeeta L. Jadhav
1
and Mohan G. Babare
2
1
Indian Institute of Food Science and Technology, Chhatrapati Sambhajinagar - 431005 (India).
2
Dr. Babasaheb Ambedkar Marathwada University, Aurangabad - 431004 (India).
DOI: https://doi.org/10.51244/IJRSI.2025.120800160
Received: 04 July 2025; Accepted: 10 July 2025; Published: 16 September2025
ABSTRACT
Aquatic macrophytes, commonly known as hydrophytes, play a crucial role in providing structural habitat that
influences fish communities. This, in turn, allows zooplankton and other macro-invertebrates to exert a top-
down control on algal growth, a process that is largely unaffected by the nutrient levels in the water body.
Nevertheless, their populations face significant threats from factors such as eutrophication, sewage discharge,
and industrial pollutants. Additionally, seasonal variations can lead to a notable decline in the diversity of these
aquatic plants. Therefore, it is vital to establish baseline data to evaluate these impacts and ensure the health of
aquatic ecosystems.
A comprehensive survey was conducted to assess the presence of submerged macrophyte populations in the
waterways of Chhatrapati Sambhajinagar District, with meticulous documentation of the results. The findings
reveal that the Chhatrapati Sambhajinagar district boasts a rich diversity of submerged macrophytes. Notably,
the district is distinguished by its significant representation of a remarkable variety of submerged macrophytes,
comprising 24 species across 9 families. The study indicates that the Hydrocharitaceae family is the most
prevalent, featuring 12 species, followed by Potamogetonaceae with 3 species, Ceratophyllaceae and
Haloragaceae with 2 species each, and Characeae, Fabaceae, Nymphaeaceae, and Pontederiaceae families,
each represented by 1 species.
Keywords: Aquatic vegetation, Management of lakes, Wetland areas, Emergent, submerged, and floating
macrophytes, Biodiversity, Water resources.
INTRODUCTION
Submerged macrophytes play a crucial role in the functioning of shallow lakes and contribute to the
maintenance of clear water conditions (Scheffer et al., 1993; Jeppesen et al., 2007). Aquatic macrophytes serve
as a refuge for small animals from predation, alter the nutrient dynamics within the ecosystem, and prevent the
resuspension of sediments, thereby regulating water turbidity, which has implications for physicochemical
water quality and biotic communities (Kristensen et al., 1992; Horppila & Nurminen, 2001).
One of the primary ways in which macrophytes affect the status of lakes is through their involvement in
nutrient cycling. Due to their ability to produce high biomass, aquatic plants possess a significant capacity for
the accumulation of biogenic compounds (Clarke & Wharton, 2001; Abdo & Da Silva, 2002). Generally, the
structural complexity and biomass of submerged macrophytes are influenced by nutrient enrichment. The
regulation of phosphorus and nitrogen is critical for sustaining the biodiversity of lake ecosystems. Phosphorus
is regarded as a key factor influencing primary production in lakes, especially for phytoplankton (Kalff, 2001).
Submerged macrophytes represent a crucial functional group within lake ecosystems (Jeppesen et al., 1997).
Nevertheless, numerous submerged macrophytes in lakes have experienced a decline or have even vanished in
recent years, both in China and globally, and there remain significant challenges in restoring all submerged
macrophytes in lakes due to the ambiguous recession mechanisms (Qin et al., 2014; Zhang et al., 2017). A
primary factor contributing to this issue is the widespread reduction in underwater light availability, which
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1779
www.rsisinternational.org
restricts the growth of submerged macrophytes (Chen et al., 2016; Jin et al., 2020). Furthermore, underwater
light availability is essential for influencing freshwater biodiversity in lakes dominated by submerged
macrophytes (Karlsson et al., 2009; Estlander et al., 2017; Yu et al., 2021).
Submerged macrophytes are essential in shallow lakes. They enhance water quality by taking up nutrients from
the water column (Jeppesen et al., 1998; Liu et al., 2018) and by stabilizing the sediment at the bottom (Wu &
Hua, 2014; Zhang et al., 2016). Furthermore, they offer food and shelter to aquatic organisms (Blindow et al.,
2014; Wood et al., 2017; Choudhury et al., 2019). Nevertheless, the proliferation of human activities and
eutrophication has led to a global decline in the population of submerged macrophytes in shallow lakes
(Jeppesen et al., 1998; Wang et al., 2014; Yu et al., 2015). Given their significance for the ecology of shallow
lakes, submerged macrophytes have garnered increasing attention, and their restoration is a critical component
in the rehabilitation of hypertrophic urban lakes (Sondergaard et al., 2010; Dai et al., 2012; Bakker et al., 2013;
Liu et al., 2020).
The restoration of submerged macrophytes in urban lakes frequently presents challenges due to various
inherent limitations, including high nutrient loading, artificially controlled water levels, and restricted littoral
zones (Guo, 2007; Van Geest et al., 2007; Mao et al., 2020). Additionally, recurrent algal blooms can
adversely affect the survival of submerged macrophytes (Kibria et al., 2012; Wang et al., 2021), with light
deficiency being a primary factor contributing to the decline of submerged macrophytes (Schelske, 2010;
Arthaud et al., 2012; Olsen et al., 2015; Zhang et al., 2016). Therefore, enhancing underwater light availability
is essential for the growth and reproduction of submerged macrophytes in urban lakes (O’Farrell et al., 2011;
Paillisson & Marion, 2011; Zhang et al., 2016). Consequently, improving underwater light through artificial
means may prove to be a beneficial strategy for restoring submerged macrophytes in urban lakes, particularly
in areas with low fish populations or where fish are absent, as this would prevent macrophyte recovery from
being impeded by fish grazing on the plants or fish predation on zooplankton, which could otherwise result in
increased phytoplankton growth and reduced light availability for macrophyte development.
Aquatic Macrophytes are also utilized as bioindicators of water pollution due to their responsiveness to
changes in water quality. They play a crucial role in mineral cycling and organic components, which in turn
influences total biomass production within aquatic ecosystems. Numerous researchers have conducted studies
related to aquatic and wetland flora across various regions of India (Mirashi, 1954; Sen & Chatterjee, 1959;
Srivastva et al., 1987; Dhote & Dikxit, 2007; Chandra et al., 2008; Jadhav & Babare, 2025).
Research on aquatic macrophytes holds significant importance for limnologists, as it aids in comprehending
the dynamics of aquatic ecosystems. For fisheries personnel, these studies serve as a catalog of fish food
sources, while pollution control experts benefit from understanding their capacity to remove nutrients. The
diversity of macrophytes has been thoroughly examined by various researchers, including Chakraborty (2008),
Vardayan (2006), Devi et al. (2004), Manorama et al. (2007), and Laishram Kamla et al. (2007). Their findings
indicate that many aquatic macrophytes can become problematic when they proliferate excessively, leading to
their classification as aquatic weeds, which poses challenges for water management. Currently, freshwater
systems are adversely affected, experiencing a decline in native biodiversity due to the influx of untreated
sewage and pollution, which significantly alters the physicochemical parameters of water, impacting both
quality and quantity. Macrophytes promote the growth of phytoplankton and facilitate the recycling of organic
matter. Additionally, submerged species at the margins function as green manure, enhancing the abundance of
zooplankton and benthic fauna. They also offer suitable breeding and sheltering habitats for macro-
invertebrates and fish (Meshram, 2003). The proliferation of aquatic macrophytes can lead to nuisance
conditions, categorizing them as aquatic weeds and raising concerns for water management. Conducting
surveys of aquatic macrophytes can provide a solid foundation for developing management plans. The
objective of the present study was to summarize the biodiversity of submerged aquatic macrophytes in the
studied area and categorize them, thereby providing essential baseline data on species diversity for the
conservation of water bodies in Chhatrapati Sambhajinagar District.
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1780
www.rsisinternational.org
MATERIALS AND METHODS
Study area:
Chhatrapati Sambhajinagar, previously known as Aurangabad, is situated in the Deccan region, primarily
within the Godavari River basin, with some areas extending into the Tapi River basin. The city is distinguished
by its hilly landscape and semi-arid climate. It is positioned at coordinates N 19° 53' 47" E 75° 23' 54", with
latitude ranging from 19 to 20 degrees north and longitude from 74 to 76 degrees east. The Ajanta mountain
range encircles the city. Chhatrapati Sambhajinagar District, formerly Aurangabad District, is a significant area
within the Marathwada region of Maharashtra (see Fig. 1). The district covers an area of 10,100 km², with
37.55% classified as urban and the remainder as rural. It is predominantly located in the Godavari River Basin,
with portions extending towards the northwest of the Tapi River Basin.
Figure 1: Map showing the location of the Chatrapati Sambhajinagar district within the study area.
The climate of Chhatrapati Sambhajinagar is semi-arid, with average annual temperatures ranging from 17 to
33 °C. The rainy season spans from June to September, followed by winter from October to February, and
summer from March to May. The majority of the district's rainfall occurs during the monsoon season, with an
average annual precipitation of 710 mm. Outside of the southwest monsoon period, when humidity levels rise,
the air in the district is typically dry. The summer months are the driest, with afternoon relative humidity
generally between 20 and 25%. Wind speeds are usually light to moderate, increasing during the latter part of
the hot season and throughout the monsoon. During the hot season, winds primarily originate from the west to
the north. In contrast, during the southwest monsoon season, they mainly come from the southwest to the
northwest. Throughout the remainder of the year, winds predominantly blow from the northeast to the
southeast, shifting to southwesterly and northwesterly directions in January and February. A significant portion
of the district is situated within the Godavari basin, while a smaller area in the northeastern region falls within
the Tapi Basin. The Godavari River, along with its tributariesPurna, Dudhna, and Shivnaserves as the
principal waterway in the district. Other notable tributaries include the Sukna, Khelna, Kham, Gulathi,
Shivbhadra, and Girija rivers. Based on the drainage patterns and geomorphological features, the district has
been comprised of 52 distinct watersheds.
Survey Methodology
Aquatic macrophytes from significant waterways and water bodies within the Chhatrapati Sambhajinagar
district study area were systematically gathered across three distinct seasons: rainy, winter, and summer.
Seasonal surveys, which included multiple visits, were carried out to gather data on both littoral and
submerged vegetation, as detailed by Narayana and Somashekar (2002). Macrophytes were collected monthly
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1781
www.rsisinternational.org
from June 2005 to May 2007 from shallow, littoral zones using the hand-picking method. Specimens were
thoroughly washed with water, excess moisture was absorbed with filter papers, and the specimens were stored
in polythene bags before being transported to the laboratory in an ice box. They were preserved in 10%
formalin and identified to the species level with the assistance of relevant literature from Edmondson (1959),
Pennack (1978), Tonapi (1980), and Fasset (2000). Over a four-year span, from June 2018 to 2022, these
surveys documented aquatic plants, particularly submerged macrophytes, through regular excursions at short
intervals to collect and identify plant samples from the designated study locations. This paper specifically
addresses the submerged macrophytes found in the Chhatrapati Sambhajinagar district.
A sufficient number of field excursions were conducted to sample and document observations throughout the
study period, ensuring the collection of significant macrophyte species. The Aquatic Plant Sampling Protocols
were carefully followed during the sampling process. Samples were manually collected from the littoral zone
and the exposed marginal areas of the sampling sites. Since most of these species are herbaceous, they were
carefully uprooted, rinsed, and cleaned to reduce mud content before being pressed between newspapers or
placed in polyethylene bags, depending on availability and field conditions, for immediate identification. This
methodology aligns with techniques employed in recent research published by Narasimha and Benarjee
(2016). The collected plant specimens were identified and verified against regional floras and pertinent
literature.
RESULTS AND DISCUSSION
This survey of aquatic plants primarily aimed to identify, document, and evaluate the abundance and
distribution of various submerged aquatic plant species within the waterways of the study area. Aquatic plants
are species that thrive in a range of saltwater and freshwater environments, including small fish tanks, home
aquariums, lakes, ponds, and oceans. These plants can grow above water, be completely submerged, or exist in
an intermediate state; the essential aspect is that they naturally thrive in wet habitats. Aquatic plants exhibit a
variety of traits that facilitate their survival in these environments (Rascio, 2002). A compilation of submerged
macrophytes identified in significant water bodies, their surrounding areas, and wetlands within the study
region (the list is representative, not comprehensive) is provided in Table 1.
Table 1: List of Submerged Macrophytes observed in major water bodies, their vicinities and wetlands in study
region (list is representative, not exhaustive)
Sr. No.
Scientific Name (Family)
Common Name
1
Cabomba caroliniana (Nymphaeaceae)
Fanwort
2
Ceratophyllum demmersum (Ceratophyllaceae)
Coontail
3
Ceratophyllum submersum (Ceratophyllaceae)
Soft Hornwort
4
Chara globularis (Characeae)
Green algae
5
Elodea canadensis (Hydrocharitaceae)
Canadian pondweed
6
Elodea densa (Hydrocharitaceae)
Brazilian pondweed
7
Elodea bifoliata (Hydrocharitaceae)
Earthpedia Plant
8
Elodea trifoliate (Hydrocharitaceae)
Pondweed
9
Heterenthera dubia (Pontederiaceae)
Water stargrass
10
Hydrilla verticillata (Hydrocharitaceae)
Oxygen weed
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1782
www.rsisinternational.org
11
Myriophyllum aquaticum (Haloragaceae)
Water milfoil/ Parrotfeather
12
Myriophyllum spicatum (Haloragaceae)
Eurasian water milfoil
13
Najas graminea (Hydrocharitaceae)
Water nymph
14
Najas guadalupensis (Hydrocharitaceae)
Guppy grass
15
Najas indica (Najadaceae)
Naiads
16
Najas minor (Najadaceae/ Hydrocharitaceae)
Water velvet/ Najas
17
Ottelia alismoids (Hydrocharitaceae)
Ottelia/ duck lettuce
18
Potamogeton crispus (Potamogetonaceae)
Curlyleaf pondweed
19
Potamogeton gramineous (Potamogetonaceae)
Pondweed
20
Potamogeton Perfoliatus (Potamogetonaceae)
Pond weed / Redhead grass
21
Trifolium fragiferum (Fabaceae)
Strawberry clover
22
Vallisneria natans (Hydrocharitaceae)
Tapegrass
23
Vallisneria Americana (Hydrocharitaceae)
Eelgrass / tapegrass
24
Vallisneria spiralis (Hydrocharitaceae)
Eelgrass /straight vallisneria
The previous studies (Jadhav & Babare, 2025) regarding emergent macrophyte vegetation in the Chhatrapati
Sambhajinagar district have shown that the Cypereaceae family is the most dominant group among the
emergent families in this area. Examining diversity indices within this district facilitates a deeper
understanding of the ecological conditions of submerged macrophytes and their functional traits. This research
provides vital baseline data related to the diversity of submerged aquatic macrophytes in the key water bodies
of the Chhatrapati Sambhajinagar district, which encompasses significant water bodies, river systems,
marshes, and wetlands. The results concerning submerged macrophytes in the Chhatrapati Sambhajinagar
district of the Marathwada region in Maharashtra are essential for managing plant growth, addressing
eutrophication, restoring aquatic ecosystems, and regulating plant species to enhance pollution control through
phytoremediation methods in the study area. The total number of submerged macrophyte species by family in
Chhatrapati Sambhajinagar District is presented in Table 2.
Table 2: Family-wise total of submerged macrophytes species in Chhatrapati Sambhajinagar District.
Sr. No.
Number of Species
1
2
2
1
3
1
4
2
5
12
6
1
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1783
www.rsisinternational.org
7
1
8
1
9
3
Total species
24 species
The investigation of submerged macrophytes in the Chhatrapati Sambhajinagar district indicates that the
Hydrocharitaceae family is the most prevalent, comprising 12 species (see Table 2). Potamogetonaceae
follows as the second most commonly found family, containing 3 species. The Ceratophyllaceae family
Haloragaceae family were noted with 2 species each, while Characeae, Fabaceae, Nymphaeaceae, and
Pontederiaceae families each have 1 species reported. The findings from the survey of Chhatrapati
Sambhajinagar District demonstrate that the Hydrocharitaceae family dominates the area with 12 species. A
graphical representation of the percentage comparison is illustrated in Fig. 2.
Fig. 2: Species percentagewise graphical representation of submerged species in Chhatrapati Sambhajinagar
Macrophytes play a significant role in ecosystem functioning. They serve as primary producers, providing
structural habitat for numerous animal species, and offer shelter and nourishment to invertebrates (Castella et
al., 1984) and fish (Rossier, 1995). Additionally, they are involved in ecosystem processes such as
biomineralization, transpiration, sedimentation, elemental cycling, material transformation, and the release of
biogenic trace gases into the atmosphere (Carpenter & Lodge, 1986). Recent research has highlighted the
critical role of aquatic macrophytes in regulating nutrient availability in water and enhancing the stability of
lakeshores (Carpenter & Lodge, 1986; Blindow et al., 2014). The composition of macrophyte assemblages can
be affected by geology, land use, and the chemistry of water and sediment (Barko et al., 1991; Lougheed et al.,
2001; del Pozo et al., 2011). The composition and distribution of macrophyte communities vary according to
climate, hydrology, substrate type, and nutrient availability.
Numerous researchers have emphasized the importance of macrophytes. Aquatic macrophytes play a crucial
role in aquatic ecosystems by providing food and shelter for invertebrates (Rejmankova, 2011) and stabilizing
sediments and shorelines, thereby reducing turbidity in aquatic systems (Bamidele & Nyamali, 2008).
Submerged macrophytes influence nutrient dynamics, light attenuation, temperature regimes, hydrodynamic
cycles, and substrate characteristics (Rooney et al., 2003). The macrophytes are responsible for regulating and
stabilizing mineral cycling in water bodies, thus serving as indicators of potential ecosystem damage
(Pieczynska & Ozimek, 1976). Aquatic plants drive ecosystem productivity and biogeochemical cycles, partly
because they act as a critical interface between sediments and the overlying water column (Carpenter & Lodge,
1986). Aquatic plants are vital components of aquatic ecosystems. Like all other photosynthetic organisms,
Ceratophyllaceae
9%
Characeae
4%
Fabaceae
4%
Haloragaceae
8%
Hydrocharitaceae
50%
Najadaceae
4%
Nymphaeaceae
4%
Pontederiaceae
4%
Potamogetonaceae
13%
Other
21%
Number of Species
Ceratophyllaceae Characeae Fabaceae Haloragaceae Hydrocharitaceae
Najadaceae Nymphaeaceae Pontederiaceae Potamogetonaceae
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1784
www.rsisinternational.org
they are essential for capturing the solar energy that fuels all other ecosystem components. They provide
oxygen to other biota and contribute to the physical habitat (Cronk & Fennessy, 2001).
Submerged macrophytes serve a crucial function as producers within food webs, providing shelter and food for
various organisms, and acting as indicators of water quality (Nieder et al., 2004). They are vital for the
diversity of zoobenthos in aquatic ecosystems, offering shelter, breeding grounds, and food sources (Ali et al.,
2007). Furthermore, submerged macrophytes generate oxygen in stagnant areas and extend the hydrologic
retention time necessary for the removal of particulate nutrients (Nepf et al., 2007). However, despite their
significance, the development of dense monotypic stands can negatively impact the diversity and abundance of
invertebrates and fish (Buchan & Padilla, 2000). Thick beds of submerged macrophytes can generate organic
matter from both actively growing and decaying plants, leading to eutrophication in the water column
(Chambers et al., 1999). Additionally, their excessive growth can obstruct water flow, block reservoir inlets,
and disrupt recreational activities (Kenneth, 1996).
In general, the growth of macrophytes is constrained by various factors including the type of substrate, water
depth, water clarity, nutrient concentration, and different physical disturbances. The presence and quantity of
submerged macrophytes are affected by both chemical and physical factors, such as water quality, availability
of light (Dennison et al., 1993), water transparency, water depth (Canfield et al., 1985), channel slope, channel
dimensions (O’Hare et al., 2011), and hydrological regime (Franklin et al., 2008). It is crucial to comprehend
how various environmental factors influence the habitats of submerged macrophytes for purposes such as flow
regulation, sediment transport (Jarvela, 2005), and evaluations of the ecological status of rivers (Clayton &
Edwards, 2006).
The presence and distribution of submerged macrophytes within river ecosystems are influenced by water
quality parameters (Nieder et al., 2004), water depth, and the velocity of water in flowing systems (Sousa,
2011). Biological elements, such as competition, herbivory, and disease, serve as significant habitat
determinants for submerged macrophytes (Lacoul & Freedman, 2006). In river ecosystems, submerged
macrophytes can transition from slow-moving streams to larger rivers following the construction of weirs (Son
et al., 2017). Consequently, it is essential to comprehend the submerged macrophytes that possess high
invasive potential for effective river management and conservation strategies. A limited number of studies
have forecasted the distributions of submerged macrophytes in rivers utilizing generalized additive models
(GAMs) (Ahmadi-Nedushan et al., 2006; Camporeale & Ridolfi, 2006). Furthermore, the GAMs that have
been developed have seldom been validated with independent field data (Guisan et al., 2002).
The conducted survey of macrophytes in the designated study area of Chhatrapati Sambhajinagar district
sought to evaluate vegetation in aquatic environments, which include water bodies, waterlogged regions,
wetlands, and marshes. The main aim of the survey was to identify ecological species from various families or
groups and to explore their diversity within the chosen area. Over the years, many researchers have
participated in similar studies, such as Asri and Aftekhari (1999), Raizi (1996), Ghahreman and Attar (2003),
Jalili et al. (2009), Zahed et al. (2013), and Naqinezhad and Hosseinzadeh (2014).
Macrophytes are beneficial for the phytoremediation of metal-contaminated wastewaters (Shingadgaon &
Chavan, 2016; 2018; 2019). The presence and distribution of submerged macrophyte species in the study area
indicate a considerable diversity, which is crucial for regulating the climatic conditions of Chhatrapati
Sambhajinagar district, located in the Marathawada region of Maharashtra. Generally, macrophytes exhibit
simpler structural complexity, as their growth predominantly occurs beneath the water's surface, rendering
them less accessible to various aquatic organisms (Singadgaon & Chavan, 2017; 2018a; 2018b). As a result, it
is frequently suggested that these species establish a uniform habitat (Daspute-Taur et al., 2018). The root
systems of emergent macrophytes are recognized for influencing the movement of solutes in the subsurface.
Moreover, it is posited that these macrophytes fulfill similar ecological roles across different trophic levels
within ecosystems; however, submerged macrophytes have not been extensively studied by researchers and
require greater attention from the scientific community, as there is currently insufficient scientific evidence to
substantiate this assertion. Thorough scientific investigation is essential to clarify the role of submerged
macrophytes in shaping aquatic habitats (Stahr & Kaemingk, 2017).
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1785
www.rsisinternational.org
CONCLUSIONS
The Chhatrapati Sambhajinagar district, situated in the Marathwada region of Maharashtra, showcases an
impressive diversity of submerged macrophytes, comprising 24 species from 9 families. The findings indicate
that the Hydrocharitaceae family is the most prevalent, containing 12 species, followed by Potamogetonaceae
and Haloragaceae families with 3 species each. The Ceratophyllaceae family was noted to have 2 species,
while Characeae, Fabaceae, Nymphaeaceae, and Pontederiaceae families were each documented with 1 species
during the study.
ACKNOWLEDGEMENTS
The authors wish to extend their sincere appreciation to Prof. B.L. Chavan, who serves as the Professor and
Head of the Department of Environmental Science at Dr. Babasaheb Ambedkar Marathwada University,
Chhatrapati Sambhajinagar (MS), for his invaluable support and enlightening discussions during the course of
this research.
REFERENCES
1. Abdo, M.S.A., & Da Silva, C.J. (2002). Nutrient stock in the aquatic macrophytes Eichhornia crassipes
and Pistia stratiotes in the PantanalBrazil. In Proceedings of the German-Brazilian Workshop on
Neotropical Ecosystems (pp. 875880).
2. Ahmadi-Nedushan, B., Van der Meer, J., & Herman, P.M.J. (2006). A generalized additive model for
the prediction of macrobenthic species distributions: A case study from the Dutch Continental Shelf.
ICES Journal of Marine Science, 63(1), 110.
3. Ali, M.M., Al-Sayed, M.N., & Hassan, S.M. (2007). The impact of aquatic macrophytes on the
distribution and abundance of macroinvertebrates in River Nile, Egypt. Egyptian Journal of Aquatic
Biology & Fisheries, 11(2), 7996.
4. Arthaud, F., Puijalon, S., & Bornette, G. (2012). Light limitation and plant strategy: The case of two
submerged macrophytes. Aquatic Botany, 96, 17.
5. Asri, Y., & Aftekhari, A.R. (1999). Study of aquatic plants in Anzali wetland. Iranian Journal of
Biology, 12(4), 1-13.
6. Bakker, L., Sarneel, J.M., Geurts, J.J.M., & Bakker, E.S. (2013). Restoration of submerged
macrophytes in shallow lakes: Challenges and opportunities. Hydrobiologia, 710(1), 111.
7. Bamidele, J.F., & Nyamali, O. (2008). Phytoremediation potential of some aquatic macrophytes in
contaminated water bodies in Delta State, Nigeria. Journal of Applied Sciences Research, 4(12), 1779
1786.
8. Barko, J.W., Gunnison, D., & Carpenter, S.R. (1991). Sediment interactions with submersed
macrophyte growth and community dynamics. Aquatic Botany, 41(1-3), 4161.
9. Blindow, I., Hargeby, A., & Hilt, S. (2014). Facilitation of clear-water conditions in shallow lakes by
macrophytes: differences between charophyte and angiosperm dominance. Hydrobiologia, 737(1), 99
110.
10. Buchan, L.A., & Padilla, D.K. (2000). Predicting the invasion of a nonindigenous aquatic plant:
Potential for spread of Hydrilla verticillata in the Great Lakes. Ecological Applications, 10(4), 1141
1151.
11. Camporeale, C., & Ridolfi, L. (2006). A generalized additive model for the distribution of aquatic
macrophytes in lowland rivers. Ecological Modelling, 194(4), 305318.
12. Canfield, D.E., Langeland, K.A., Maceina, M.J., Hall, D.M., & Haller, W.T. (1985). Relationships
between aquatic macrophyte biomass and nutrient standing crops in Florida lakes. Journal of Aquatic
Plant Management, 23, 7377.
13. Carpenter, S.R., & Lodge, D.M. (1986). Effects of submersed macrophytes on ecosystem processes.
Aquatic Botany, 26, 341370.
14. Castella, E., Richardot-Coulet, M., Roux, C., & Richoux, P. (1984). Macroinvertebrates as "describers"
of physicochemical changes in a French river polluted by a paper mill. Environmental Pollution Series
A, Ecological and Biological, 34(3), 215233.
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1786
www.rsisinternational.org
15. Chakraborty, D. (2008). Diversity of aquatic macrophytes of two wetland areas of North Bengal, India.
Journal of Environmental Biology, 29(5), 785788.
16. Chambers, P.A., Prepas, E.E., Hamilton, H.R., & Bothwell, M.L. (1999). The effect of aquatic
macrophytes on nutrient concentrations in lakes: A review. Canadian Journal of Fisheries and Aquatic
Sciences, 56(5), 734747.
17. Chandra, S., Asthana, A., & Singh, R.K. (2008). Diversity of aquatic macrophytes in selected water
bodies of Lucknow, Uttar Pradesh. Nature and Science, 6(4), 1014.
18. Chen, J., Cao, T., Zhang, X., Xi, Y., Ni, L., & Jeppesen, E. (2016). Differential photosynthetic and
morphological adaptations to low light affect depth distribution of two submersed macrophytes in
lakes. Scientific Reports, 6, 34028. doi: 10.1038/srep34028
19. Choudhury, M.I., Urrutia-Cordero, P., Zhang, H., Ekvall, M.K., Medeiros, L.R., & Hansson, L.A.
(2019). Charophytes collapse beyond a critical warming and brownification threshold in shallow lake
systems. Science of The Total Environment, 661, 148154.
20. Clarke, S.J., & Wharton, G. (2001). Sediment nutrient characteristics and aquatic macrophytes in
lowland English rivers. Science of The Total Environment, 266, 103112.
21. Clayton, J.S., & Edwards, T.L. (2006). Ecological monitoring of aquatic plants in New Zealand lakes.
Hydrobiologia, 557(1), 173184.
22. Cronk, J.K., & Fennessy, W. (2001). Wetland Plants: Biology and Ecology. CRC Press.
23. Dai, Y., Jia, C., Liang, W., Hu, S.H., & Wu, Z.B. (2012). Effects of the submerged macrophyte
Ceratophyllum demersum L. on restoration of a eutrophic waterbody and its optimal coverage.
Ecological Engineering, 40, 113116.
24. Daspute-Taur, V., Singadgaon, S.R., & Chavan, B.L. (2018). The study of structural complexity of
aquatic macrophytes and its effects on macroinvertebrate communities. International Journal of
Research in Pharmacy and Biological Sciences, 5(2), 1621.
25. del Pozo, R., Rodrigo, M.J., & Casas, A.M. (2011). Macrophyte assemblages as indicators of
environmental quality in Mediterranean rivers. Limnetica, 30(1), 105118.
26. Dennison, W.C., Orth, R.J., Moore, K.A., Stevenson, J.C., Carter, V., Kollar, S., ... & Wetzel, R.G.
(1993). Assessing water quality with submerged aquatic vegetation: The Chesapeake Bay example.
BioScience, 43(2), 8694.
27. Devi, M.B., Singh, M.K., & Singh, P.K. (2004). Macrophyte diversity and community structure in
Loktak Lake, Manipur, India. Lakes & Reservoirs: Research and Management, 9(3), 209218.
28. Dhote, S., & Dikxit, A.K. (2007). Aquatic macrophytes and their conservation in Madhya Pradesh,
India. Journal of Environmental Biology, 28(2), 341345.
29. Edmondson, W.T. (1959). Freshwater Biology. John Wiley & Sons.
30. Estlander, S., Horppila, J., Olin, M., & Nurminen, L. (2017). Should I stay or should I go? The diurnal
behaviour of plant-attached zooplankton in lakes with different water transparency. Journal of
Limnology, 76(2), 253260. doi: 10.4081/jlimnol.2017.1564
31. Fasset, N.C. (2000). A Manual of Aquatic Plants. University of Wisconsin Press.
32. Franklin, P.A., Dunbar, M.J., & Dawson, F.H. (2008). Classification of macrophyte assemblages in
British rivers: Relationships with environmental factors and implications for ecological status. Aquatic
Conservation: Marine and Freshwater Ecosystems, 18(7), 9901006.
33. Ghahreman, A., & Attar, F. (2003). Flora of Iran. Ministry of Culture and Islamic Guidance.
34. Guisan, A., Lehmann, A., Ferrier, S., Austin, M., Scott, A.P., & Thuiller, W. (2002). Modelling the
distribution of plant and animal species with environmental factors using generalized additive models.
*Ec
REFERENCES
1. crassipes and Pistia stratiotes in the PantanalBrazil. In Proceedings of the German-Brazilian
Workshop on Neotropical Ecosystems (pp. 875880).
2. Ahmadi-Nedushan, B., St-Hilaire, A., Bérubé, M., Robichaud, É., Thiémonge, N., & Bobée, B. (2006).
A review of statistical methods for the evaluation of aquatic habitat suitability for instream flow
assessment. River Research and Applications, 22(4), 503523.
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1787
www.rsisinternational.org
3. Ali, M. M., Mageed, A. A., & Heikal, M. (2007). Importance of aquatic macrophyte for invertebrate
diversity in large subtropical reservoir. Limnologica - Ecology and Management of Inland Waters,
37(2), 155169.
4. Arthaud, F., Mousset, M., Vallod, D., Robin, J., Wezel, A., & Bornette, G. (2012). Effect of light stress
from phytoplankton on the relationship between aquatic vegetation and the propagule bank in shallow
lakes. Freshwater Biology, 57(3), 666675.
5. Asri, Y., & Eftekhari, T. (1999). Flora and vegetation of Siah-Keshim lagoon. Journal of
Environmental Studies, 28, 119.
6. Bakker, E. S., Sarneel, J. M., Gulati, R. D., Liu, Z., & Donk, E. (2013). Restoring macrophyte diversity
in shallow temperate lakes: Biotic versus abiotic constraints. Hydrobiologia, 710(1), 2337.
7. Bamidele, J. F., & Nyamali, B. (2008). Ecological studies of the Ossiomo river with reference to the
macrophytic vegetation. Research Journal Botany, 3(1), 2934.
8. Barko, J. W., Gunnison, D., & Carpenter, S. R. (1991). Sediment interactions with submerged
macrophyte growth and community dynamics. Aquatic Botany, 41, 4165.
9. Blindow, I., Hargeby, A., & Hilt, S. (2014). Facilitation of clear-water conditions in shallow lakes by
macrophytes: Differences between charophyte and angiosperm dominance. Hydrobiologia, 737(1), 99
110.
10. Buchan, L. A. J., & Padilla, D. K. (2000). Predicting the likelihood of Eurasian watermilfoil presence
in lakes: A macrophyte monitoring tool. Ecological Applications, 10(5), 14421455.
11. Camporeale, C., & Ridolfi, L. (2006). Riparian vegetation distribution induced by river flow
variability: A stochastic approach. Water Resources Research, 42(10), W10415.
https://doi.org/10.1029/2006WR004933
12. Canfield, D., Langeland, K., Linda, S., & Haller, W. (1985). Relations between water transparency and
maximum depth of macrophyte colonization in lakes. Journal of Aquatic Plant Management, 23, 25
28.
13. Carpenter, S. R., & Lodge, D. M. (1986). Effects of submerged macrophytes on ecosystem processes.
Aquatic Botany, 26(3-4), 341370.
14. Castella, E., Richardot-Coulet, M., Roux, C., & Richoux, P. (1984). Macro-invertebrates as descriptors
of morphological and hydrological types of aquatic ecosystems abandoned by the Rhone River.
Hydrobiologia, 119(3), 219226.
15. Chakraborty, A., Jha, B. C., & Bhakat, R. K. (2008). Diversity and impact of macrophytes in
Bandardaha Beel, Murshidabad, West Bengal. Indian Journal of Environmental & Ecoplan, 15(1-2),
331335.
16. Chambers, P. A., DeWreede, R. E., Irlandi, E. A., & Vandermeulen, H. (1999). Management issues in
aquatic macrophyte ecology: A Canadian perspective. Canadian Journal of Botany, 77(3), 471487.
17. Chandra, G., Bhattacharji, I., Ghosh, A., & Chatterji, S. N. (2008). Mosquito control by larvivorous
fishesA review. Indian Journal of Medical Research, 127(1), 1327.
18. Chen, J., Cao, T., Zhang, X., Xi, Y., Ni, L., & Jeppesen, E. (2016). Differential photosynthetic and
morphological adaptations to low light affect depth distribution of two submerged macrophytes in
lakes. Scientific Reports, 6, 34028. https://doi.org/10.1038/srep34028
19. Choudhury, M. I., Urrutia-Cordero, P., Zhang, H., Ekvall, M. K., Medeiros, L. R., & Hansson, L. A.
(2019). Charophytes collapse beyond a critical warming and brownification threshold in shallow lake
systems. Science of the Total Environment, 661, 148154.
20. Clarke, S. J., & Wharton, G. (2001). Sediment nutrient characteristics and aquatic macrophytes in
lowland English rivers. Science of the Total Environment, 266(1-3), 103112.
21. Clayton, J., & Edwards, T. (2006). Aquatic plants as environmental indicators of ecological condition
in New Zealand lakes. Hydrobiologia, 570(1), 147151.
22. Cook, C. D. K., & Urmi-König, K. (1984). A revision of the genus Hydrilla (Hydrocharitaceae).
Aquatic Botany, 17(1), 110.
23. Cronk, J. K., & Fennessy, M. S. (2001). Wetland Plants: Biology and Ecology. CRC Press/Lewis
Publishers.
24. Dai, Y., Jia, C., Liang, W., Hu, S. H., & Wu, Z. B. (2012). Effects of the submerged macrophyte
Ceratophyllum demersum on restoration of a eutrophic waterbody and its optimal coverage. Ecological
Engineering, 40, 113116.
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1788
www.rsisinternational.org
25. Daspute-Taur, A. B., Thete-Jadhav, R. G., Jadhav, S. L., Shingadgaon, S. S., & Chavan, B. L. (2018a).
An application of floating constructed wetland reactor to phytoremediation of sewage. International
Research Journal of Natural and Applied Sciences, 5(2), 136144.
26. Daspute-Taur, A. B., Thete-Jadhav, R. G., Jadhav, S. L., Shingadgaon, S. S., & Chavan, B. L. (2018b).
The use of a floating constructed wetland reactor for the phytoremediation of sewage. International
Research Journal of Natural and Applied Sciences, 5(2), 136144.
27. del Pozo, R., Fernandez-Alaez, C., & Fernandez-Alaez, M. (2011). The relative importance of natural
and anthropogenic effects on community composition of aquatic macrophytes in Mediterranean ponds.
Marine and Freshwater Research, 62(1), 101109.
28. Dennison, W. C., Orth, R. J., Moore, K. A., Stevenson, J. C., Carter, V., Kollar, S., Bergstrom, P. W.,
& Batiuk, R. A. (1993). Assessing water quality with submersed aquatic vegetation. BioScience, 43(2),
8694.
29. Devi Beenakumari, N., & Sharma, M. B. (2004). Life form analysis of the macrophytes of the Loktak
Lake, Manipur, India. In A. Arvindkumar (Ed.), Biodiversity and Diversity (pp. 1923). A.P.H.
Corporation.
30. Dhote, S., & Dixit, S. (2009). Water quality improvement through macrophytesA review.
Environmental Monitoring and Assessment, 152(1-4), 149153.
31. Edmondson, W. T. (1959). Fresh Water Ecology (2nd ed.). John Wiley & Sons, Inc.
32. Estlander, S., Horppila, J., Olin, M., & Nurminen, L. (2017). Should I stay or should I go? The diurnal
behaviour of plant-attached zooplankton in lakes with different water transparency. Journal of
Limnology, 76(2), 253260. https://doi.org/10.4081/jlimnol.2017.1564
33. Fassett, N. C. (2000). A Manual of Aquatic Plants. Agrobios (India).
34. Franklin, P., Dunbar, M., & Whitehead, P. (2008). Flow controls on lowland river macrophytes: A
review. Science of the Total Environment, 400(1-3), 369378.
35. Freitas, A., & Thomaz, S. M. (2011). Inorganic carbon storage may limit the development of
submerged macrophytes in habitats of the Paraná River Basin. Acta Limnologica Brasiliensia, 23(1),
5762.
36. Ghahreman, A., & Attar, F. (2003). The Anzali Wetland: A critical ecological and floristic study.
Journal of Environmental Studies (Special Issue on Anzali Lagoon), 28, 138. (Published in Persian
with an English summary).
37. Guisan, A., Edwards, T. C., & Hastie, T. (2002). Generalized linear and generalized additive models in
studies of species distributions: Setting the scene. Ecological Modelling, 157(2-3), 89100.
38. Guo, L. (2007). EcologyDoing battle with the green monster of Taihu Lake. Science, 317(5842),
1166.
39. Haynes, R. R., & Holm-Nielsen, L. B. (1985). A generic treatment of Potamogeton L.
(Potamogetonaceae). Nordic Journal of Botany, 5(6), 577592.
40. Horppila, J., & Nurminen, L. (2001). Effects of different macrophyte growth forms on sediment and P
resuspension in a shallow lake. Hydrobiologia, 545(1), 167175.
41. Jadhav, S. L., & Babare, M. G. (2025a). Investigation of emergent aquatic macrophytes in the
Chhatrapati Sambhajinagar District. International Journal of Research Publication and Reviews, 6(3),
73227329.
42. Jadhav, S. L., & Babare, M. G. (2025b). Bioconcentration Factor (BCF), Bioaccumulation Factor
(BAF), Metal Enrichment Factor (MEF) and Metal Translocation Factor (MTF) for the submerged
macrophyte species Ceratophyllum demersum. International Journal of Innovative Research in
Technology, 11(11), 19031913.
43. Jadhav, S. L., & Babare, M. G. (2025c). Screening of Azolla caroliniana for metal related bio-potential
factors. International Journal of Innovative Science and Research Technology, 10(4), 143154.
44. Jadhav, S. L., & Babare, M. G. (2025d). Survey of emergent aquatic macrophytes in the District of
Dharashiv of Maharashtra. International Journal of Recent Advances in Multidisciplinary Research,
12(4), 1104211048.
45. Jadhav, S. L., & Babare, M. G. (2025e). Bioabsorption, bioconcentration, metal enrichment and metal
transfer factors of toxic metals in Arundo donax L. International Journal of Novel Research and
Development, 10(4), e619e629.
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1789
www.rsisinternational.org
46. Jadhav, S. L., & Babare, M. G. (2025f). Investigation of emergent aquatic macrophytes in Jalna District
of Maharashtra. International Journal of Creative Research Thoughts, 13(4), 19071919.
47. Jadhav, S. L., & Babare, M. G. (2025g). Bio potential factors of the aquatic plant species
Ceratophyllum submersum: BCF, BAF, MEF, and MTF. International Journal of Novel Research and
Development, 10(4), f771f785.
48. Jadhav, S. L., & Babare, M. G. (2025h). Survey of submerged aquatic macrophytes in Beed District,
Maharashtra. International Journal of Science, Architecture, Technology and Environment, 2(5), 287
300.
49. Jadhav, S. L. (2025i). Survey of submerged aquatic macrophytes in the District of Dharashiv of
Maharashtra. International Journal of Advanced Scientific and Technical Research, 2(1), 194203.
https://doi.org/10.26808/RS.2025.87c51a
50. Jalili, A., Hamzehee, B., Asri, Y., Shirvani, A., Khushnivis, M., & Pak Parvar, M. (2009). Identifying
dominant ecological vegetation patterns in Anzali Wetland and their significance for ecosystem
management. Journal of Sciences, University of Tehran, 35(1), 5157.
51. Jarvela, J. (2005). Effect of submerged flexible vegetation on flow structure and resistance. Journal of
Hydrology, 307(1-4), 233241.
52. Jeppesen, E., Søndergaard, M., & Christoffersen, K. (Eds.). (1997). The structuring role of submerged
macrophytes in lakes. Springer-Verlag.
53. Jeppesen, E., Søndergaard, M., Meerhoff, M., Lauridsen, T. L., & Jensen, J. P. (2007). Shallow lake
restoration by nutrient loading reduction: Some recent findings and challenges ahead. Hydrobiologia,
584(1), 239252.
54. Jeppesen, E., Søndergaard, M., & Christoffersen, K. (1998). The Structuring Role of Submerged
Macrophytes in Lakes. Springer.
55. Jin, S., Ibrahim, M., Muhammad, S., Khan, S., & Li, G. (2020). Light intensity effects on the growth
and biomass production of submerged macrophytes in different water strata. Arabian Journal of
Geosciences, 13, 17. https://doi.org/10.1007/s12517-020-05924-4
56. Kalff, J. (2001). Limnology. Prentice Hall.
57. Karlsson, J., Byström, P., Ask, J., Ask, P., Persson, L., & Jansson, M. (2009). Light limitation of
nutrient-poor lake ecosystems. Nature, 460(7254), 506509. https://doi.org/10.1038/nature08179
58. Kenneth, A. L. (1996). Hydrilla verticillata (L.F.) Royle (Hydrocharitaceae), "The perfect aquatic
weed". Castanea, 61(3), 293304.
59. Kibria, G., Lau, T. C., & Wu, R. (2012). Innovative 'Artificial Mussels' technology for assessing spatial
and temporal distribution of metals in Goulburn-Murray catchments waterways, Victoria, Australia:
Effects of climate variability (dry vs. wet years). Environmental International, 50, 3846.
60. Kristensen, P., Søndergaard, M., & Jeppesen, E. (1992). Resuspension in a shallow eutrophic lake.
Hydrobiologia, 228(2), 101109.
61. Lacoul, P., & Freedman, B. (2006). Environmental influences on aquatic plants in freshwater
ecosystems. Environmental Reviews, 14(2), 89136. https://doi.org/10.1139/a06-001
62. Laishram, K. D., & Sharma, M. (2007). Life form analysis and biological spectrum of the macrophytes
of the Laisoipat lake, Manipur. Indian Journal of Environmental & Ecoplan, 14(1-2), 153159.
63. Les, D. H. (1988). The origin and affinities of the Ceratophyllaceae. Taxon, 37(2), 345367.
64. Liu, H., Zhou, W., Li, X. W., Chu, Q. S., Tang, N., Shu, B. Z., Liu, G. H., & Xing, W. (2020). How
many submerged macrophyte species are needed to improve water clarity and quality in Yangtze
floodplain lakes? Science of the Total Environment, 724, 138267.
65. Liu, Z. W., Hu, J. R., Zhong, P., Zhang, X. F., Ning, J. J., Larsen, S. E., Chen, D. Y., Gao, Y. M., He,
H., & Jeppesen, E. (2018). Successful restoration of a tropical shallow eutrophic lake: Strong bottom-
up but weak top-down effects recorded. Water Research, 146, 8897.
66. Lougheed, V. L., Crosbie, B., & Chow-Fraser, P. (2001). Primary determinants of macrophyte
community structure in 62 marshes across the Great Lakes basin: Latitude, land use, and water quality
effects. Canadian Journal of Fisheries and Aquatic Sciences, 58(8), 16031612.
67. Manorama, T. D., & Sharma, M. (2007). Studies on the distribution of macrophytes of Yenapat Lake,
Bishnupur, Manipur. Indian Journal of Environmental & Ecoplan, 14(1-2), 311318.
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1790
www.rsisinternational.org
68. Mao, Z., Gu, X., Cao, Y., Luo, J. H., Zeng, Q. F., Chen, H. H., & Jeppesen, E. (2020). Pelagic energy
flow supports the food web of a shallow lake following a dramatic regime shift driven by water level
changes. Science of the Total Environment, 756, 143642.
69. Meshram, C. B. (2003). Macro-invertebrate fauna of Lake Wadali, Amravati, Maharashtra. Journal of
Aquatic Biology, 18(2), 4750.
70. Middelboe, A. L., & Markager, S. (1997). Depth limits and minimum light requirements of freshwater
macrophytes. Freshwater Biology, 37(3), 553568.
71. Mirishi, M. V. (1954). Studies on the hydrophytes of Nagpur. Journal of the Indian Botanical Society,
33, 298308.
72. Naqinezhad, A. R., & Hosseinzadeh, F. (2014). Plant diversity of Fereydoonkenar International
wetland, Mazandaran. Journal of Plant Researches (Iranian Journal of Biology), 27(2), 320335.
73. Narasimha, R. K., & Banargee, G. (2016). The diversity and distribution of macrophytes in
Nagaramtank, situated in the Warangal district of Telangana state. International Journal of Fisheries
and Aquatic Studies, 4(1), 270275.
74. Narayana, J., & Somashekhar, R. K. (2002). Macrophytes diversity in relation to water quality
investigation on river Cauvery. In A. Kumar (Ed.), Ecology and conservation of lakes, reservoirs and
rivers (pp. 86113). A.B.D. Publishers.
75. Nepf, H., Ghisalberti, M., White, B., & Murphy, E. (2007). Retention time and dispersion associated
with submerged aquatic canopies. Water Resources Research, 43(4), W04422.
76. Nieder, W. C., Barnaba, E., Findlay, S. E. G., Hoskins, S., Holochuck, N., & Blair, E. A. (2004).
Distribution and abundance of submerged aquatic vegetation and Trapa natans in the Hudson River
Estuary. Journal of Coastal Research, 20(Special Issue 41), 150161.
77. O’Farrell, I., Izaguirre, I., Chaparro, G., Unrein, F., Sinistro, R., Pizarro, H., Rodriguez, P., Pinto, P. D.,
Lombardo, R., & Tell, G. (2011). Water level as the main driver of the alternation between a free-
floating plant and a phytoplankton dominated state: A long-term study in a floodplain lake. Aquatic
Sciences, 73(2), 275287.
78. O’Hare, J. M., O’Hare, M. T., Gurnell, A. M., Dunbar, M. J., Scarlett, P. M., & Laizé, C. (2011).
Physical constraints on the distribution of macrophytes linked with flow and sediment dynamics in
British rivers. River Research and Applications, 27(6), 671683.
79. Olsen, S., Chan, F., Li, W., Zhao, S. T., Søndergaard, M., & Jeppesen, E. (2015). Strong impact of
nitrogen loading on submerged macrophytes and algae: A long-term mesocosm experiment in a
shallow Chinese lake. Freshwater Biology, 60(7), 15251536.
80. Paillisson, J. M., & Marion, L. (2011). Water level fluctuations for managing excessive plant biomass
in shallow lakes. Ecological Engineering, 37(2), 241247.
81. Pennak, R. W. (1978). Fresh Water Invertebrates of the United States (2nd ed.). Wiley Interscience
Publishers, John Wiley & Sons.
82. Pieczynska, F., & Ozimek, T. (1976). Ecological significance of lake macrophytes. International
Journal of Ecology and Environmental Sciences, 2, 115128.
83. Qin, B., Zhang, Y., Gao, G., Zhu, G., Gong, Z., & Dong, B. (2014). Key factors affecting lake
ecological restoration. Progress in Geography, 33(7), 918924. https://doi.org/10.1007-
6301(2014)33:7& lt;918:HPSTHF>2.0.TX;2-9
84. Rascio, N. (2002). The underwater life of secondarily aquatic plants: Challenges and solutions. Critical
Reviews in Plant Sciences, 21(5), 401427.
85. Rejmankova, E. (2011). The role of macrophytes in wetland ecosystems. Journal of Ecology and Field
Biology, 34(4), 333345.
86. Riazi, B. (1996). Siah-Keshim, The Protected Area of Anzali Wetland. Department of the Environment
Press.
87. Rooney, V. J. N., Girwat, M. W., & Savin, M. C. (2005). Links between phytoplankton and bacterial
community dynamics in a coastal marine environment. Microbial Ecology, 49(1), 163175.
88. Rossier, O. (1995). Spatial and temporal separation of littoral zone fishes of Lake Geneva
(SwitzerlandFrance). Hydrobiologia, 300-301(1), 321327.
89. Scheffer, M., Hosper, S. H., Meijer, M. L., Moss, B., & Jeppesen, E. (1993). Alternative equilibria in
shallow lakes. Trends in Ecology & Evolution, 8(8), 275279.
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1791
www.rsisinternational.org
90. Schelske, C. L., Lowe, E. F., Kenney, W. F., Battoe, L. E., Brenner, M., & Coveney, M. F. (2010).
How anthropogenic darkening of Lake Apopka induced benthic light limitation and forced the shift
from macrophyte to phytoplankton dominance. Limnology and Oceanography, 55(3), 12011212.
91. Sculthorpe, C. D. (1967). The Biology of Aquatic Vascular Plants. Edward Arnold.
92. Sen, D. N., & Chetterjee, U. N. (1959). Ecological studies on aquatic and swampy vegetation of
Gorakhpur. A survey. Agra University Journal of Research (Science), 8(1), 1727.
93. Shingadgaon, S. S., & Chavan, B. L. (2018a). The potential for zinc absorption in Water Lettuce (Pistia
Stratiotes, Linn). International Journal of Science and Research, 7(3), 14971504.
94. Shingadgaon, S. S., & Chavan, B. L. (2018b). Zinc uptake potential of Eichhornia crassipes at various
concentrations. International Journal for Research in Applied Science & Engineering Technology, 6(3),
34723476.
95. Shingadgaon, S. S., & Chavan, B. L. (2018c). Zinc uptake potential in Cyperus esculentus L.
International Journal of Application or Innovation in Engineering & Management, 7(6), 4758.
96. Shingadgaon, S. S., & Chavan, B. L. (2019). Assessment of Bioaccumulation Factor (BAF),
Bioconcentration Factor (BCF), Translocation Factor (TF), and Metal Enrichment Factor (MEF)
capabilities of aquatic macrophyte species exposed to metal-contaminated wastewater. International
Journal of Innovative Research in Science, Engineering and Technology, 8(1), 329347.
97. Short, F. T., & Coles, R. G. (1999). Global seagrass research: an update. Aquatic Botany, 63(3-4), 185-
191.
98. Sondergaard, M., Johansson, L. S., Lauridsen, T. L., Jørgensen, T. B., Liboriussen, L., & Jeppesen, E.
(2010). Submerged macrophytes as indicators of the ecological quality of lakes. Freshwater Biology,
55(5), 893908.
99. Son, D., Cho, K.-H., & Lee, E. J. (2017). The potential habitats of two submerged macrophytes,
Myriophyllum spicatum and Hydrilla verticillata in the river ecosystems, South Korea. Knowledge and
Management of Aquatic Ecosystems, 418, 58.
100. Sousa, W. (2011). Hydrilla verticillata (Hydrocharitaceae), a recent invader threatening Brazil’s
freshwater environments: A review of the extent of the problem. Hydrobiologia, 669(1), 120.
101. Srivastava, A. K., Dixit, S. N., & Singh, S. K. (1987). Aquatic angiosperm of Gorakhpur. Indian
Journal of Forestry, 10(1), 4657.
102. Stahr, K. J., & Kaemingk, M. A. (2017). An evaluation of emergent macrophytes and their role in
supporting various aquatic species. Lake and Reservoir Management, 33(3), 314323.
103. Thete-Jadhav, R. G., Daspute, A. B., Jadhav, S. L., Shingadgaon, S. S., & Chavan, B. L. (2018a).
Sewage treatment by Floating Constructed Wetland Reactor System. Journal of Emerging
Technologies and Innovative Research, 5(12), 406413.
104. Thete-Jadhav, R. B., Daspute-Taur, A. B., Jadhav, S. L., Shingadgaon, S. S., & Chavan, B. L. (2018b).
Performance of Floating Constructed Wetland Reactor with Cyperus esculentus L. macrophyte at
different concentrations of sewage. International Journal of Application or Innovation in Engineering &
Management, 7(2), 611.
105. Tonapi, G. T. (1980). Fresh Water Animals of India, An Ecological Approach. Oxford and IBH
Publishing Co.
106. Van Geest, G. J., Coops, H., Scheffer, M., & Nes, E. (2007). Long transients near the ghost of a stable
state in eutrophic shallow lakes with fluctuating water levels. Ecosystems, 10(1), 3646.
107. Vardayan, L., & Ingole, B. S. (2006). Studies on heavy metal accumulation in aquatic macrophytes
from seven lakes: Armenia and Caranbolim. Internet Collection, 127.
108. Wang, H. J., Wang, H. Z., Liang, X. M., & Wu, S. K. (2014). Total phosphorus thresholds for regime
shifts are nearly equal in subtropical and temperate shallow lakes with moderate depths and areas.
Freshwater Biology, 59(12), 16591671.
109. Wang, Y., Pedersen, M. W., Alsos, I. G., De Sanctis, B., Racimo, F., Prohaska, A., Coissac, E., Owens,
H. L., Merkel, M. K. F., Fernandez-Guerra, A., Rouillard, A., Lammers, Y., Alberti, A., Denoeud, F.,
Money, D., Ruter, A. H., McColl, H., Larsen, N. K., Cherezova, A. A., & Willerslev, E. (2021). Late
Quaternary dynamics of Arctic biota from ancient environmental genomics. Nature, 600(7887), 8692.
https://doi.org/10.1038/s41586-021-04016-x
110. Wood, K. A., O’Hare, M. T., McDonald, C., Searle, K. R., Daunt, F., & Stillman, R. A. (2017).
Herbivore regulation of plant abundance in aquatic ecosystems. Biological Reviews, 92(2), 11281141.
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1792
www.rsisinternational.org
111. Wu, D., & Hua, Z. (2014). The effect of vegetation on sediment resuspension and phosphorus release
under hydrodynamic disturbance in shallow lakes. Ecological Engineering, 69, 5562.
112. Yu, Q., Wang, H. Z., Li, Y., Shao, J. C., Liang, X. M., Jeppesen, E., & Wang, H. J. (2015). Effects of
high nitrogen concentrations on the growth of submerged macrophytes at moderate phosphorus
concentrations. Water Research, 83, 385395.
113. Yu, Y. X., Li, Y., Wang, H. J., Wu, X. D., Zhang, M., Wang, H. Z., Hamilton, D. P., & Jeppesen, E.
(2021). Submerged macrophyte restoration with artificial light-emitting diodes: A mesocosm
experiment. Ecotoxicology and Environmental Safety, 228, 113044.
https://doi.org/10.1016/j.ecoenv.2021.113044
114. Zahed, S., Asri, Y., Yousefi, M., & Moradi, A. (2013). The flora, life forms, and chorotypes of plants
in Selkeh Lagoon, Northern Iran. Journal of Plant Researches (Iranian Journal of Biology), 26(3), 301
310.
115. Zhang, Y. L., Liu, X. H., Qin, B. Q., Shi, K., Deng, J. M., & Zhou, Y. Q. (2016). Aquatic vegetation in
response to increased eutrophication and degraded light climate in eastern Lake Taihu: Implications for
lake ecological restoration. Scientific Reports, 6, 23867.
116. Zhang, Y., Jeppesen, E., Liu, X., Qin, B., Shi, K., Zhou, Y., Thomaz, S. M., & Deng, J. M. (2017).
Global loss of aquatic vegetation in lakes. Earth-Science Reviews, 173, 259265.
https://doi.org/10.1016/j.earscirev.2017.08.013
Daspute-Taur, A. B., Thete-Jadhav, R. G., Jadhav, S. L., Shingadgaon, S. S., & Chavan, B. L. (2018a).
*An application of floating constructed wetland reactor to phytoremediation of sewage*. IRJNAS,
5(2), 136144.
Daspute-Taur, A. B., Thete-Jadhav, R. G., Jadhav, S. L., Shingadgaon, S. S., & Chavan, B. L. (2018b).
*The use of a floating constructed wetland reactor for the phytoremediation of sewage*. IRJNAS, 5(2),
136144.
Jadhav, S. L. (2025i). *Survey of submerged aquatic macrophytes in the District of Dharashiv of
Maharashtra*. IJSATR, 2(1), 194203. [https://doi.org/10.26808/RS.2025.87c51a]
(https://doi.org/10.26808/RS.2025.87c51a)
Jadhav, S. L., & Babare, M. G. (2025a). *Investigation of emergent aquatic macrophytes in the
Chhatrapati Sambhajinagar District*. IJRP\&R, 6(3), 73227329.
Jadhav, S. L., & Babare, M. G. (2025b). *BCF, BAF, MEF and MTF for Ceratophyllum demersum*.
IJIRT, 11(11), 19031913.
Jadhav, S. L., & Babare, M. G. (2025c). *Screening of Azolla caroliniana for metal related bio-
potential factors*. IJISRT, 10(4), 143154.
Jadhav, S. L., & Babare, M. G. (2025d). *Survey of emergent aquatic macrophytes in the District of
Dharashiv of Maharashtra*. IJRAMR, 12(4), 1104211048.
Jadhav, S. L., & Babare, M. G. (2025e). *Bioabsorption, bioconcentration, metal enrichment and metal
transfer factors in Arundo donax L.* IJNRD, 10(4), e619e629.
Jadhav, S. L., & Babare, M. G. (2025f). *Investigation of emergent aquatic macrophytes in Jalna
District of Maharashtra*. IJCRT, 13(4), 19071919.
Jadhav, S. L., & Babare, M. G. (2025g). *Bio potential factors of Ceratophyllum submersum: BCF,
BAF, MEF, and MTF*. IJNRD, 10(4), f771f785.
Jadhav, S. L., & Babare, M. G. (2025h). *Survey of submerged aquatic macrophytes in Beed District,
Maharashtra*. IJSATE, 2(5), 287300.
Shingadgaon, S. S., & Chavan, B. L. (2018a). *Zinc absorption in Water Lettuce (Pistia stratiotes)*.
IJSR, 7(3), 14971504.
Shingadgaon, S. S., & Chavan, B. L. (2018b). *Zinc uptake potential of Eichhornia crassipes*.
IJRASET, 6(3), 34723476.
Shingadgaon, S. S., & Chavan, B. L. (2018c). *Zinc uptake potential in Cyperus esculentus L.*
IJAEM, 7(6), 4758.
Shingadgaon, S. S., & Chavan, B. L. (2019). *Assessment of BAF, BCF, TF, and MEF of aquatic
macrophytes*. IJIRSET, 8(1), 329347.
REFERENCES
INTERNATIONAL JOURNAL OF RESEARCH AND SCIENTIFIC INNOVATION (IJRSI)
ISSN No. 2321-2705 | DOI: 10.51244/IJRSI |Volume XII Issue VIII August 2025
Page 1793
www.rsisinternational.org
1. A D Adoni. Workbook on limnology. Prathibha Publication, 1985, C-10, 6 Gouri Nagar, Sagar-
470003.
2. C D K Cook. Aquatic Plant Book, 2nd Edition. SPB Academic Publishing, 1996, New York.
3. I. H. Chung and S. S. Jeng. Hevy metal pollution in the Ta-Tu River. Bulletin of the Institute of
Zoology, Academy of Science 1974; 13, 67-73.
4. Asmita B Daspute-Taur, Renuka G. Thete-Jadhav, S.L. Jadhav, Shankar S. Shingadgaon, B.L. Chavan.
An application of floating constructed wetland reactor to phytoremediation of sewage. International
Research Journal of Natural and Applied Sciences 2018;5(2), 136-144.
5. KU Garad, RD Gore, and SP Gaikwad. A Synoptic Account of the Flora of Solapur District,
Maharashtra, India. Biodiversity Data Journal, 2015, DOI: 10.3897/BDJ.3.e4282.
6. OP Gupta. Weedy Aquatic Plants: Their Utility, Menace, and Management. Agrobios, Jodhpur, India,
2001. p. 273.
7. AN Henry, V Chitra and NP Balakrishnan, Flora of Tamil Nadu, India. Botanical Survey of India,
Southern Circle, Coimbatore, 1989; 1(3), 1-171.
8. SK Jain, RR Rao. A Handbook of Field and Herbarium Methods. Today and Tomorrow, 1976. New
Delhi.
9. K Subramanyam, Aquatic Angiosperms. Botanical Monograph (3). 1962. CSIR, New Delhi.
10. SR Yadav and MM Sardesai. Flora of Kolhapur District. Shivaji Univesity, 2002. Kolhapur.
11. RK Narasimha and G Banargee. The diversity and distribution of macrophytes in Nagaramtank, located
in the Warangal district of Telangana state. International Journal of Fisheries and Aquatic Studies
2016; 4(1), 270-275.
12. J Narayana and RK Somashekar. Macrophytic diversity in relation to water quality in the River
Cauvery. Ecology and Conservation of Lakes, Reservoirs, and Rivers, 2002. ABD Publishers in Jaipur,
India.
13. RN Mandal, AK Datta, N Sarangi and PK Mukhopadhya. A review on the diversity of aquatic
macrophytes as food and feed components for herbivorous fish. Indian Journal of Fisheries. 2010,
57(3), 65-73.
14. JI Nirmal Kumar, H Soni, RN Kumar and I Bhatt. The role of macrophytes in the phytoremediation of
heavy metal-contaminated water and sediments in the Pariyej Community Reserve, Gujarat, India.
Turkish Journal of Fisheries and Aquatic Sciences,2008, 8, 193-200.
15. MT Philipose. Current trends in weed control in fish culture water across Asia and Far East. FAO Fish
Report, 44(5), 25-52.
16. A Sharma and PK Singhal. Impact of floating and emergent vegetation on the trophic status of a
trophical lake:The macrophytes and physico-chemical status. J Env Biol., 1988, 9(3), 303-311.
17. SS Shingadgaon and BL Chavan. Evaluation of Bioaccumulation Factor (BAF), Bioconcentration
Factor (BCF), Translocation Factor (TF) and Metal Enrichment Factor (MEF) Abilities of Aquatic
Macrophyte Species Exposed to Metal Contaminated Wastewater. International Journal of Innovative
Research in Science, Engineering and Technology, 2019, 8 (1), 329-347.
18. SS Shingadgaon and BL Chavan. Zinc Uptake Potential of Eichhornia Crassipes at Various
Concentrations. International Journal for Research in Applied Science & Engineering Technology,
2018, 6(III), 3472-3476.
19. SS Shingadgaon and BL Chavan. Zinc Uptake Potential in Water Lettuce (Pistia Stratiotes, Linn).
International Journal of Science and Research. 2016, 1497-1504.
20. SS Shingadgaon and BL Chavan. Zinc Uptake Potential in Cyperous esculentus, Linn. Innovation in
Engineering & Management (IJAIEM). 2018, 7(6), 47-58.
21. KJ Stahr and MA Kaemingk. An assessment of emergent macrophytes and their utilization by various
aquatic taxa. Lake and Reservoir Management, 2017, 33(3), p. 314-323.
22. WR. World Resources report. 2000, USA.
23. WR. World Resources. 2001, UK.
24. RG Wetzel. The importance of scientific foundations in constructed wetlands. Constructed Wetlands
for Water Quality Improvement CRC Press, Boca Raton, FL: Lewis Publishers, Inc. 1993, p. 3-7.
Jadhav & Babare’s series of regional surveys in Maharashtra (Chhatrapati Sambhajinagar, Dharashiv, Jalna,
Beed) documented the distribution of emergent aquatic macrophytes.