Abstract
Aquatic macrophytes are crucial within the inland waters of the Niger Delta as they enhance the surrounding, act as a dwelling region for minute water creatures, and make a contribution considerably to fisheries productivity. Aquatic macrophytes also provide substrates, meal, and habitat for aquatic animals, in addition to enhancing habitat physical structure and organic complexity, which will increase biodiversity in our water bodies. Macrophytes have crucial characteristics in our water bodies. Nonetheless, rather mild attention is paid to their protection, and if they are not properly managed, they can become out of control and cause issues. This article looks at the ecology, benefits, and drawbacks of common aquatic macrophytes in Nigeria’s Niger Delta, in addition to great strategies for controlling the macrophytes in the inland waters of the Niger Delta. Managing aquatic macrophytes in this region is to accomplish stability in the environment by controlling extreme foray of plant species. A thorough assessment of the nature, scope, and potential of aquatic macrophyte problems is required before implementing control measures. Management actions in this region must raise awareness among the local population.
Access provided by Autonomous University of Puebla. Download chapter PDF
Similar content being viewed by others
Keywords
3.1 Introduction
Inland water basins in Nigeria offer crucial habitat for a variety of flora and aquatic fauna, which support the areas they surround. However, activities (synthetic and native) that caused ecological concerns have recently damaged the connected ecological system, affecting the provided natural resources. Despite this, not much is established as regards aquatic bodies with plants and wildlife, stock-taking, socio-economic, and conservation in Nigeria (Daddy et al. 1993). Nigeria’s Niger Delta is among the significant deltas with natural resources such as crude oil, gas, animals, beneficial plants, and other resources abound in the region. It is the world’s sixth largest producer and exporter of crude oil. It encompasses a diverse range of natural zones, including sand ridge barriers, brackish mangroves, and freshwater swamps (Udo 1987). The Niger Delta spans 20,000 km2 and is surrounded by 70,000 km2 of natural wetlands. The physically generated flood plains cover 7.5% of the 923,800 km2 entire surface. This incredibly well-endowed ecological system harbors great biodiversity around the sphere. It also sustains abundant species, with additional species of freshwater organisms than any other ecological system in West Africa (Akinbode 2005; Vida 2010).
3.1.1 Aquatic Macrophyte Ecology
Macro-flora with roots that grow constantly or intermittently in aquatic environments is usually referred to as “aquatic macrophytes.” They are a category of big, macroscopic photosynthetic organisms that grow in an aquatic environment (Jones et al. 2012). They are floras that grow in the presence of standing water that is at or above the soil’s surface. Different water bodies and culture systems are examples of standing water. Plants having photosynthetic components that are always or occasionally underwater or detached in water and evident to the naked eye are known as macrophytes (Cook 1990). Macrophytes are significant parts of the brook environment since they boost the structure of habitats and increase biodiversity (Wetzel 2001; Pelicice et al. 2008). Furthermore, both animate and inanimate aquatic macrophytes can serve as food sources for other creatures (Lopes et al. 2007). They are important in the hydro-environment because they provide a spawning substratum for species such as fin fish, insects, and plankton, and they also help as fish diet (Ratusshnyale 2008). Excessive macrophyte growth might have detrimental consequences in most rivers and lakes (Bini et al. 2005).
Many individuals are unaware of the relevance of macrophytes in our aquatic environment. Macrophytes have an important function in water bodies and pastoral populations. Sadly, minute attention is given to their conservation. Aquatic macrophytes have not been given attention, and this is regrettable as fluctuations in macrophyte assemblage could be particularly predictive key urban stress classes. Water quality is thought to be influenced by the health and structure of macrophyte populations (Suren 2000; Balanson et al. 2005).
Despite the current focus on fisheries research and development in Nigerian waters, little attention has been paid to the non-fish resources that go with them (aquatic macrophytes). Aquatic plants, particularly in freshwater ecology, have a scarcity of information. The current trend of fully destroying these resources without first gaining a thorough understanding of their ecology, population dynamics, and socioeconomic significance could signal doom for other aquatic resources that rely on them. They offer recreational and medical value in a well-balanced environment. However, with a case study of the Niger Delta region and knowledge of the ecological characteristics and possible uses of these resources, better management, protection, and conservation of aquatic macrophytes in Nigerian water bodies would be required (Ita et al. 1985). This article looks at the ecology, species, distribution, and abundance of macrophytes in the Niger Delta region, Nigeria.
3.2 Macrophyte Taxonomy Groups
Macrophytes are a wide range collecion of taxonomic groups that come in a variety of forms and dimensions, in a particular, totally submerged, and others drift on the water’s surface. Despite the fact that they are vital to our aquatic ecology, many still don’t value them. The location of the plant in relation to the surface and substrate. Macrophytes are frequently divided into four categories: floating unattached, floating attached, submerged, and emergent (Puijalon et al. 2008). Aquatic macrophytes are aesthetically beautiful and environmentally beneficial when used in moderation. They are described as essential components of a river’s aging process. Though they can be found in deep, clean lakes and rivers, their presence is not guaranteed. An abundance of aquatic macrophytes represents a sign of “middle” or “old” age. In large quantities, they can interfere positively or negatively with some water uses (Okaeme et al. 1999) (Fig. 3.1) (Table 3.1).
3.3 Ecological Functions of Aquatic Macrophytes
Various forms of aquatic ecosystems rely heavily on macrophyte plants. Aquatic macrophytes are present in a variety of aquatic habitats, and their occurrence is of benefit to fisheries and pastoralism in the basins. Macrophytes are important for not just the biological community but also the natural processes, which take place in the aquatic environment. There are benefits to macrophytes’ performance in an aquatic ecological system. The commonly found macrophytes in the Niger delta region is shown in Plates 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 3.10, 3.11, 3.12.
3.3.1 Fisheries Production
Aquatic plants are regarded as undervalued components of the aquatic ecosystem. It does, however, play an important part in the fishing industry. Herbivorous fishes like Tilapia zillii, locally farmed, rely on aquatic plants as a food source. Some fishes consume Lemna paucicostata species (Mbagwu and Adeniji 1988). According to known information, 37 freshwater herbivorous fish species feed on macrophytes and belong to 24 families (Opuszynski and Shireman 1995). More specifically, periphytic algae that grow on the surface of aquatic plants serve as food for some fish species. Oreochromis eats coarser things, such as macrophytes, than other members of the genus (Ezeri et al. 2003). Macrophytes have been shown to provide breeding sites and refuge for fish. Carnivorous fish fingerlings feed on aquatic plants till their intestines mature to take animals, according to Agbogidi et al. (2000).
3.3.2 Habitat for Water Organisms
Smaller animals use aquatic macrophytes as a home. These little animals play an important role in ecology because they feed fish. Studies have shown that vegetated regions harbor fewer organisms than non-vegetated ones (Agbogidi et al. 2000). Many fishes find shelter, spawning substrates, and nursery sites under the leaves of Ceratophyllum demersum and Myriophyllum spicatum. Aquatic macrophytes provide cover for juvenile fish from predatory fish, making them a vital nursery for baby fish (juveniles). Water lettuce provides a safe haven for fish and crustaceans from predatory fish (ICAAE 1992). Heterotis niloticus makes its nest out of aquatic macrophytes, but Gymnarchus niloticus spawns in stagnant waters containing macrophytes and then migrates to flowing waters (Meske 1985). Freshwater and marine plants have an impact on animal and aquatic organism communities through a series of habitat-related mechanisms, such as providing nurseries, dwelling spaces, and feeding areas (Hyndes et al. 2018).
3.3.3 Healthy Ecosystem/Nutrient Cycling
In the aquatic environment, some macrophytes perform a dynamic function in a healthy ecosystem that produces oxygen via photosynthesis and provide a substrate and cover for various species. They also help stabilize the sediments together. This helps increase water clarity and reduce the volume of pollution released into the environment through sediment erosion (Kumar et al. 2020).
Agbogidi et al. (2000) reported that the sewage is channeled through macrophytes in order to assimilate and decrease the nutrient concentrations prior to discharge inside the water body. Macrophytes are exploited in bio-manipulation to boost fish culture (Dar et al. 2011). They absorb large amounts of nutrients as a means of removing nutrients from effluent (Uka et al. 2009). Macrophytes are used in phytoremediation procedures of polluted water bodies and in engineered structures known as “constructed swamps” for the treatment and decontamination of wastes (Vymazal 2013). They are also an indicator of water quality by absorbing excess nutrients (Petre 1990).
3.3.4 Source of Alternative Medicine
Traditional communities also use a variety of macrophytes in healing therapy. As a result, a significant portion of these ethnobotanical materials may yield molecules that could be employed as modern medicine and pharmaceuticals (Olayide 1981). Polygonum senegalense is mashed with soda ash and used for rheumatoid arthritis, according to Kio and Ola-Adams (1987). Water lettuce is also employed for treating “flu,” according to Obot and Ayeni et al. (1999). According to Bubayero (1986), most Nigerians patronize traditional healers. Most of these macrophytes produce chemicals that are extremely promising for application in current medications and pharmaceuticals. The species fever in youngsters and is used as a dewormer and eye ointments. It’s regularly used with clay in Ghana to prevent abortion. The root of Ethulia conyzoides is used to relieve constipation when blended with red pepper.
3.3.5 Industrial Uses
Aquatic macrophytes variety of resources that could be beneficial in industries, construction, matting, bedding, and pulp or paper. In Northern Nigeria, the dry root of C. maculatus is used for perfume, and the ripe silky inflorescences of T. australis are utilized in padding pillows (Ita 1993). The leaves of C. asticulatus have mosquito resistance, and their stems are utilized in multicolored mats (Kio and Ola-Adams 1990). Vossia cuspidata, Cyperus papyrus, and Eichornia crassipes have monetary value for pulp, paper, and fiber. Raphia vinifera is used as a raw material for brushes, brooms, and mats (Okojie 1995).
3.3.6 Sources of Energy
Aquatic flora as a source of energy, according to, Edewor (1998), is primarily used as a fuel for fish smoking and residential energy. Aquatic floras can become liquid, gaseous, or stable fuels through bio-methanation, fermentation, and pyrolysis, in line with reviews from different growing countries. Eichornia crassipes is digested without delay in China and India to make biogas, which is used to generate electricity to rural regions at a low cost. Stems of Aeschynomene crassicaulis and Cyperus papyrus are used as fuel for domestic cooking and fish smoking (Kio and Ola-Adams 1987).
3.4 Aquatic Macrophytes as Nuisance
Macrophytes produce an explosively excessive population, when the environment changes as a result of pollution. Aquatic macrophytes play an essential function in maintaining the richness and role of the aquatic environment. Several of these macrophytes can be unsafe when in abundance. When non-native species are purposely or by accident brought into places where they have no natural enemies to limit their growth, they are able to produce massive, uncontrollable populations. Plants developing in an aquatic environment can become dense (Chambers et al. 2008). The nuisance macrophytes cause:
3.4.1 Effect on Water Body
A floating mat of macrophyte vegetation can hinder sunlight from reaching the surface of water, which results in low natural food, eventually affecting fish production. The bloom of macrophyte vegetation causes enormous fish mortality due to the excessive oxygen requirement and contest for available nutrients. These invasive aquatic macrophytes have a negative effect on water condition and biodiversity (Uka et al. 2009). Submerged macrophytes degrade breeding grounds (particularly almonds). Dense macrophytes can cause a huge variation in oxygen, putting several fish species at risk. Similarly, when photosynthesis is lower than respiration, fish death may occur.
3.4.2 Hindrance to Navigation
Towering macrophytes above and submerged in water prevent entry, impede navigation, and damage hydroelectric infrastructure, and floating mats obstruct watercraft transportation routes. The lifestyle of a floating mat makes the aquatic surrounding insecure due to the hazard of craft, the penetration of massive predatory aquatic animals, and additional mechanical problems. It additionally has an effect on fish nets within the surrounding. Macrophytes halt boats through the means of winding round their propellers. Macrophyte mats, inclusive of water hyacinth, may even block a ship (Mandal 2007).
3.4.3 Habitat for Spread of Diseases
While certain aquatic macrophytes prevent disease-supporting organisms, others create the best surroundings for them. Most individual ailments are spread through transitional hosts, which are reliant on certain macrophytes for completion of their cycle. Blocked waterways as a result of floral vegetation or infestation of Pistia stratiotes harbor schistosomiasis (African sleeping sickness). An aquatic snail that dwells among flora serves as the intermediate host. Anything that brings this deoxygenated water to the surface (such as high wind) reduces the oxygen level in the water column, resulting in fish fatalities. As a result of this, even if the fish does not die, continuous low oxygen levels weaken the fish, and it grows to be extra susceptible to illnesses. The tranquil aquatic surrounding that macrophyte growth can create is optimal for mosquito larvae development (Bromilow 2010).
3.5 Interaction Between Macrophytes and Environmental Variables
This interplay is a considerable function of the aquatic surrounding that is vital for aquatic movement and ecological function (Xia et al. 2010). Though increase and spread are regular occurrences in water bodies, actions like agriculture, building, and development initiatives have increased concern about aquatic macrophytes and water quality in recent years (Wang et al. 2009). According to Dienye et al. (2017), the interplay confirmed that as pH and dissolved oxygen decreased through the wet season, the extent of macrophyte abundance increased while salinity increased. Dense macrophytes were slightly influenced by salinity in the Niger Delta vicinity. As the temperature rises, fewer species become abundant, while macrophytes in the vicinity decline in abundance. Chemical oxygen demand was negatively correlated with all species, and biological oxygen demand was positively correlated with all species of macrophytes. BOD increases due to dead organic matter, which supports macrophyte abundance. Therefore, pH, dissolved oxygen, and chemical oxygen demand affect the distribution and abundance in the region.
3.5.1 Methods of Managing Macrophytes
The number one goal of coping with flora in the Niger Delta is to create a balance in the ecological system through monitoring the intense invasion of various macrophyte species. The ways of controlling aquatic macrophytes include:
3.5.2 Precautionary Control
There are special ways by which macrophytes get into our waters: fishermen’s nets, boats, ballast waters, wind, birds, and more. However, precautionary measures begin with either reduction or total eradication of the sources. Plants should never be rinsed into aquatic surrounding wherever they can develop and regrow.
3.5.3 Machine-Driven Control
It involves uprooting or raking the macrophytes out of the soil. Some aquatic floras are recurrent and possess roots that could resprout, and harvesting growth beneath is vital for efficient management. Mechanical weed harvesters with submerged blades are beneficial for larger bodies of water, according to McComas (1993). The principle of the operation these harvesters used is like that of lawn mowing. The macrophytes will not be eliminated but cannot get to the surface and cause problems. Crop the harvested flora and discard it appropriately, so it won’t be re-introduced into the water while mechanically regulating the aquatic macrophytes. If left to float in a body of water, the harvested flora fragments can sprout new ones.
3.5.4 Biological Control
For biological management, lots of strange and natural organisms have been used. Beneficial organisms are used to prevent the spread of macrophytes in this approach. People could also rely on introducing animal or microbe that can feed on poisonous floras. Nevertheless, when the incorrect type of management is implemented, this process could have terrible effect for the environment (Gallagher and Haller 1990). Biological control measures are:
3.5.4.1 Water Plants (Macrophytes)
Introduction of certain desirable aquatic flora has the capacity to eradicate aquatic nuisance species. Native macrophytes, on the alternative, are generally desirable since they have more control with the surrounding ecosystem. Invasive species can effortlessly displace desirable macrophytes, and this approach can be tough, but when the invasive plants are eliminated, this method works well.
3.5.4.2 Herbivorous Fish Species
Herbivores can help to keep aquatic flora abundance under check; to help decrease aquatic flora, grass carp is adopted. They’ve been advanced genetically to stop breeding to consume the flora. When the surroundings are advantageous, the Chinese grass carp (Ctenopharyngodon idella) will eat up aquatic macrophytes, and this is temperature dependent. Their activities have minute result below 16 °C but attain a peak at 25 °C. Grass carp are choosy eaters, desiring soft flora over fibrous ones (Wells and Clayton 2005).
3.5.4.3 Microorganisms (Bacteria)
Bacteria and fungus are also used to regulate macrophyte richness. Those that live on different floras can be exploited to control the flora selectively. These macrophytes die due to contamination when the microorganisms are introduced, while the more needed plants will be spared.
3.5.5 Chemical Control
When rightly applied, herbicides overpower aquatic macrophyte plants without inflicting damage to fish or wildlife. In few instances, herbicides can be employed to manage definite floral species while sparing others. It can function as part of an aquatic plant control approach when treating few vegetative areas leaving others untreated. “Contact herbicides” kill the contact plant part. Translocated herbicides do no longer kill plant as swiftly but alternatively enter the plant itself. Generally, only the latter groups are efficient for decreasing perennial floral regrowth. They are separated as selective (killing definite plants) and non-selective (killing all plants).
Herbicide remedy can be expensive and may only afford temporary result from the fundamental problem, which is habitually enriched waterways. One should also note that when pesticides destroy aquatic flora, they decompose and discharge their stored nutrients into the aquatic surrounding, and it encourages successive growth of aquatic plants, which repeatedly necessitates additional medications. The following are examples of treatment:
3.5.6 Diquat Herbicide
This is a contact herbicide that is principally active at managing aquatic weeds and algae in a short period of time, and it’s normally sprayed on aquatic plants. This treatment will make the treated flora to quickly die and turn brown. REWARD is a standard diquat herbicide logo that works effectively on floating macrophytes and is absolutely safe to use. When the water is muddy, diquat herbicide should no longer be used as soil debris absorb it in the water (Netherland et al. 1997).
3.5.7 Fluridone Herbicide
The herbicide fluid-like non-touch herbicide that is more gradual in method than diquat. Fluridone principally controls submerged flora, and its brand tag is SONAR. It works for 30–90 days. When it is applied, it demonstrates signs for 1–2 weeks. The plants lose its green color and change to white.
3.5.8 Glyphosate
Glyphosate is available only as liquid and it controls plants above water. It is not effective for submerged plants. AquaMaster, AquaPro and Rodeo are trade names. It is prohibited to use glyphosate chemicals not explicitly branded for aquatic use (Getsinger 1998).
3.7 Conclusion and Recommendations
In spite of the opinion about aquatic plants causing a nuisance to the surrounding, they can be ecologically welcoming, when combined with mechanical method of control, which permits riparian communities to sustain dependable but long-term aquatic flora control at a reduced cost and with added economic benefits. Industrial activities in the Niger Delta vicinity should be thoroughly monitored since they have an effect on macrophytes, which are important for fish production. They offer substrates, food, and habitat for aquatic animals, in addition to enhanced habitat physical structure and biological complexity, which increases biodiversity in water bodies. The plants can only be managed and kept within tolerable limits if they are controlled properly, with some used on a long-term basis. Aquatic macrophyte utilization can only be successful on a long-term basis if their habitat is correctly handled, and this necessitates preservation of the environment. Management initiatives, on the other hand, should create awareness among the local populace. A thorough assessment of the nature, scope, and potential of aquatic macrophyte problems is required before implementing control measures.
References
Agbogidi OM, Bamidele JE, Ekokotu PA, Olele NF (2000) The role and management of aquatic macrophytes in fisheries and aquaculture. Issues Anim sci 10:221–235
Akinbode A (2005) Introductory environmental resource management. Daybis Limited, Ibadan
Ayeni JSO, Obot EA and Daddy F (1999) Aspects of the biology, conservation and management of aquatic vascular plant resources of Nigerian wetland based on the Kainji Lake experience. Proceedings of a workshop on sustainable management and conservation of fisheries and other aquatic resources of Lake Chad and the arid zone of Nigeria, Jan 16-17, Maiduguri. pp 144–145
Balanson PC, Mac MJ, Smith SB (2005) Challenges in the development and use of ecological indicators. Eco ind 1:3–10
Bini LM, Oliveria LG, Souza DC, Cavalho P, Pinto MP (2005) Patterns of the aquatic macrophytes cover in Cachoeira dourada Reservoir Brazil. J Fish Biol 65(1):19–24
Bromilow C (2010) Problem plants and alien weeds of South Africa. Briza Publication, Pretoria, p 243
Bubayero AM (1986) Traditional medicine in the science of man. In: Sofowara A (ed) The state of medicinal plants research in Nigeria, pp 129–133
Chambers PA, Lacoul P, Murphy KJ, Thomaz SM (2008) Global diversity of aquatic macrophytes in freshwater. Hydrobiologia 198:9–26. https://doi.org/10.1007/978-1-4020-8259-7_2
Cook CDK (1990) Aquatic plant book. SBP Academic, The Hague, pp 110–112
Daddy F, Adesina GO, Bankole NO, Isah U and Owotunse S (1993) Flora and fauna resources associated with Kainji, Jebba, Shriroro and Wuya water bodies in. NIFFR annual report. pp 25–27
Dar SH, Kumawat DM, Singh N, Wani KA (2011) Sewage treatment potential of water hyacinth (Eichhornia crassipes). Res J Environmental Science 5:377–385
Davidson NC, D’Cruz R, Finlayson CM (2005) Ecosystems and human Well-being: wetlands and water synthesis: a report of the millennium ecosystem assessment. World Resources Institute, Washington, DC, p 68
Dienye HE (2014) Seasonal distribution and abundance of Macrophyte of the new Calabar River Niger Delta. M.Sc. thesis, Department of Animal And Environmental Biology, Faculty of Science, University of Port Harcourt) (Unpublished). p 112
Dienye HE (2015) Species diversity of Macrophytes of the new Calabar River, Niger Delta, Nigeria. Int J Fisheries Aquatic Studies 3(1):409–413
Dienye HE, Olopade OA, Woke GN (2017) The Relationship between aquatic Macrophytes and water quality in new Calabar River Niger Delta Nigeria. Int J Res Agric Forestr 4(10):1–6
Edewor JO (1998) Developing water hyacinth from menace status to national profitable level. The proceedings of the international workshop/seminar on water hyacinth. pp 15–17
Ezeri GNO, Gabriel, Ashade OO (2003) Effects of partial shading by water lettuce (Pistia stratiotes) on growth of tank cultured Oreochromis niloticus. Fortschr Zool 2:29–38
Gallagher JE, Haller WT (1990) History and development of aquatic weed control in the United States. Rev Weed Sci 5:115–192
Getsinger KD (1998) Chemical control research in the Corps of Engineers. J Aquat Plant Manage 36:61–64
Hyndes GA, Francour P, Guidetti P, Heck KL Jr, Jenkins G (2018) The roles of seagrasses in structuring associated fish assemblages and fisheries. In: Larkum AWD et al (eds) Seagrasses of Australia. Springer, New York, pp 589–627. https://doi.org/10.1007/978-3-319-71354-0_18
ICAAE (1992) Introduction to fish culture in ponds international Centre for aquaculture and aquatic environments. Auburn University, Alabama
Ita EO (1993) Inland fishery resources of Nigeria. CIFA occasional paper no. 20 CIFA/OP 20FAO of the UN Rome. pp 120
Ita EO, Sado EK, Balogun JK, Pandogari A and Ibitoye B (1985) Inventory survey of Nigeria inland waters and their fisheries resources in: preliminary checklist of inland water bodies in Nigeria with special reference to ponds, lakes, reservoir and major rivers. Kainji Lake research institute technical report series. pp 14–51
Jones JI, Collins AL, Naden PS, Sear DA (2012) The relationship between fine sediment and macrophytes in rivers. River Res Appl 28:1006–1018
Kio PRO, Ola-Adams BA (1987) Economic importance of aquatic macropytes. In: Iloba C (ed) Ecological implications in the development of water bodies in Nigeria. National Institute for Fresh water Fisheries Research, New Bussa, pp 112–157
Kio PRO, Ola-Adams BA (1990) Utilization and development of wetlands. In: Akpata TVA, Okali DUU (eds) Nigerian wetlands, pp 41–53
Kumar V, Kumar P, Singh J, Kumar P (2020) Potential of water fern (Azolla pinnata R. Br.) in phytoremediation of integrated industrial effluent of SIIDCUL, Haridwar, India: removal of physicochemical and heavy metal pollutants. Int J Phytoremediation 22(4):392–403
Lopes CA, Benedito-Cecilio E, Martinelli LA (2007) Variability in the carbon isotope signature of Prochilodus lineatus (Prochilodontidae, Characiformes) a bottom-feeding fish of the Neotropical region. J Fish Biol 70:1649–1659
Mandal RC (2007) Weed Weediade and weed control: principles and practice, 1st edn. Agrobios, Delhi, pp 128–154
Mbagwu IG, Adeniji HA (1988) The nutritional content of duckweed Lemna paucicostata (Hegelm) in the Kainji lake area, Nigeria. Aquat Bot 29:357–366
McComas S (1993) Lake smarts: the first Lake maintenance handbook. Terrene Institute, Washington DC
Meske C (1985) Fish aquaculture: technology and experiments. Pergamon press, New York, p 33
Netherland MD, Getsinger KD, Skogerboe JD (1997) Mesocosm evaluation of the species-selective potential of fluridone. J Aquat Plant Manage 35:41–50
Okaeme AN, Olatunde AA and Ayeni JOS (1999) Lake Chad and arid zones fisheries proceeding and conservation of fisheries and other aquatic resources of Lake Chad and arid zone of Nigeria. New Bussa NIFFR. pp 202
Okojie AO (1995) Strategy for sustainable development and utilization of aquatic and wetland resources in Nigeria. In Sustainable utilization of aquatic/wetland resources. 9th/10th Annual Conference of National Association of Aquatic Science (NAAS). pp 25–32
Olayide SO (1981) Scientific research and the Nigerian economy. Ibadan University Press, Ibadan, p 83
Opuszynski K, Shireman JV (1995) Herbivorous fishes: culture and use for weed management. CRC Press, Boca Raton
Pelicice FM, Thomas SM, Agostinhno AA (2008) Simple relationships to predict attributes of fish assemblages in patches of submerged macrophytes. Neotrop Khthyol 6:543–550
Petre T (1990) Fish, fisheries aquatic macrophytes and water quality in inland waters. Water Qual Bull 12:103–106
Puijalon S, Boumo TJ, Van Groenedael J, Bormette G (2008) Clonal plasticity of aquatic plants species submitted to mechanical stress: escape versus resistance strategy. Ann Bot 102:989–996
Ratusshnyale AA (2008) The role of aquatic macrophytes in hydro ecosystem of the Kuibysheu reservoir. J Agric Environ Sci 4(1):01–08
Suren L (2000) Urban drainage impacts a receiving waters quality water. Sci Technol 27:151–158
Udo RK (1987) A comprehensive geography of West Africa. Heinemann Educational Books, Ibadan
Uka UN, Mohammed HA, Ovie SI (2009) Current diversity of aquatic macrophytes in Nigerian freshwater ecosystem. Brazil J Aquat Sci Technol 13:9–15
Vida J (2010) Nigeria’s agony dwarfs the Gulf oil spill: the US and Europe ignore it. https://www.theguardian.com/world/2010/may/30/oil-spills-nigeria-niger-delta-shell
Vymazal J (2013) Emergent plants used in free water surface constructed wetlands: a review. Ecol Eng 61:582–592. https://doi.org/10.1016/j.ecoleng.2013.06.023
Wang SR, Jin XC, Jiao LX, WU F.C. (2009) Response in root morphology and nutrient contents of Myriophyllum, spicatum to sediment type. Ecol Eng 35:1264–1270
Wells RDS, Clayton JS (2005) Mechanical and chemical control of aquatic weeds; cost and benefits. In: encyclopedia of pest management. Taylor and Francis, London. https://doi.org/10.1081/EPM-120024643
Wetzel RG (2001) Limnology: lake and river ecosystems. Academic, San diego
Xia C, Wang X, Xia J, Liu G (2010) The effect of temperature, water level on seed germination of Myriophyllum spicatom and Potamogeton malaianus. Aqaut Bot 92:28–32
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2023 The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Dienye, H.E. (2023). Aquatic Macrophytes: Ecology, Function, and Services in Niger Delta, Nigeria. In: Kumar, S., Bauddh, K., Singh, R., Kumar, N., Kumar, R. (eds) Aquatic Macrophytes: Ecology, Functions and Services. Springer, Singapore. https://doi.org/10.1007/978-981-99-3822-3_3
Download citation
DOI: https://doi.org/10.1007/978-981-99-3822-3_3
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-99-3821-6
Online ISBN: 978-981-99-3822-3
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)