Back
 OJE  Vol.7 No.13 , December 2017
Invasion of Water Hyacinth (Eichhornia crassipes) Is Associated with Decline in Macrophyte Biodiversity in an Ethiopian Rift-Valley Lake—Abaya
Abstract: Macrophytes play critical ecological role in inland water bodies, especially in shallow systems. Water hyacinth (Eichhornia crassipes) is an invasive plant species introduced to Ethiopian water bodies around the mid 20th century with recently exacerbated devastating ecological and economic consequences. Here we report the impact of the invasive plant species on macrophyte species assemblage and biodiversity in Lake Abaya, southwestern Ethiopia. We compared four sites in Lake Abaya, two hyacinth infested and two non-infested, each site consisting of 15 plots. Our results showed that water hyacinth affects the macrophyte community composition, abundance and diversity negatively. Even though some macrophyte species from the Poaceae and Cyperaceae families appear to coexist with the alien plant, the invasive species has reduced macrophyte abundance and diversity at the infested sites, and in some cases changed the community to nearly monotypic flora. Our data affirm that water hyacinth has the potential to alter macrophyte composition, abundance and diversity in the wider Ethiopian aquatic ecosystems. A broad & closer, systematic and comprehensive look at the short and long term consequences of its expanding invasion within the framework of specific local environmental, ecological and societal conditions is long-overdue.

1. Introduction

Wetland ecosystems are dynamic in their physical and chemical conditions [1] . Macrophytes, as an integral component of wetlands and shallow lakes, play critical ecological role such as nutrient cycling, and nitrogen removal through denitrification coupled with nitrification. They possess a set of complex adaptations that enable them flourish under a set of dynamic environmental factors: frequent water wave disturbance, siltation and exposure to chemical effluents from terrestrial systems. Competition within the community is also a common feature, especially within plant species having similar ecological strategies, a factor well recognized to affect species distribution in aquatic habitats [2] . Competition among aquatic plant species, however, is much more complex than known for terrestrial plants because aquatic ones can acquire inorganic carbon and nutrients in water [3] . Often, outcompeting species have better morphological and physiological adaptations for nutrient utilization; allelopathic resistance and resistance to anoxic condition than the rest.

Invasion of aquatic habitats by non-native species is a global environmental challenge with serious ecological, social and economic consequences [4] . They do this by altering soil and water chemistry, nutrient cycling, hydrology and disturbance regime of the infested ecosystem. Besides, they affect seedling recruitment blocking seed dispersal through their thick mat growth of stem, root and rhizome [5] . As a result, they often outcompete native plant species and establish a monotypic community.

Water hyacinth (Eichhornia crassipes), as an introduced non-native, is a menace to global aquatic environments with serious and devastating consequences. The genus Eichhornia has seven species and only one, i.e. E. crassipes, seems to hold the exceptional ability to be invasive. This species has the potential to multiply aggressively through clonal means of reproduction, has high growth rate and a highly dispersive floating form [6] [7] . The ecological, social and economic impact of this invasive species is complex and multifaceted: it drastically affects the physical & chemical properties of the water by reducing temperature, pH, biological oxygen demand and nutrient level. High organic load can lead to anoxic conditions that impact not only denizens of the water column, such as fish and zooplankton, but those in the sediment too. Water hyacinth can create unimpenetrable fortress in shallow areas making it difficult to access deeper parts of water bodies for recreation, fishing, transportation etc. The mat can even hamper water flow to hydo-electric dams. In some areas it can provide excessive surface area for intermediate hosts such as snails that transmit waterborne diseases such as schistosomiasis. Its control has been a continuous challenge to ecologists and there seem to be a recent shift in focus from eliminating this invasive plant to making use of its excessive biomass: source of biofuel, carbon for cellulase, electricity, food, antioxidants, medicine, animal feed, fertilizer, and for the manufacture of household articles [8] .

Water hyacinth has been reported to invade two major areas of Ethiopia: the Nile basin and the Awash basin extending down to the rift-valley region [9] . Studies on this invasive species in Ethiopia have addressed various aspects such as economic impact, biodiversity loss etc. However there is almost no data on how this aquatic weed is impacting other macrophytes in invaded water bodies. Here we report findings of a comparative study that assessed macrophyte community abundance and biodiversity in one of the most southern Ethiopian lakes, Lake Abaya. We hypothesized that water hyacinth, when present, will outcompete other macrophytes and will overall reduce the biodiversity of macrophyte communities.

2. Materials and Methods

2.1. Description of Study Area

2.1.1. Location of the Study Area

Lake Abaya is one of the two southernmost Rift Valley lakes in Ethiopia. It is the second largest lake in the country next to the non-rift valley―Lake Tana, a lake that has recently been overrun by water hyacinth, similar to Lake Abaya. Abaya is located between 5˚55'9"N to 6˚35'30"N latitude and 37˚36'90"E to 38˚03'45"E longitude (Figure 1). The lake, including its islands, has a total area of 1108.9 km2 [10] . It has a maximum length of 79.2 km and with the maximum width of 27.1 km. The mean and the maximum depth are 8.6 m and 24.5 m, respectively [11] . It is located at an average altitude of 1235 meter above sea level [10] . The study was conducted on Lake Abaya, from May to June 2016.

Figure 1. Map of study area showing Lake Abaya and sampling sites (red rectangles are sampling sites infested with water hyacinth, white rectangles are non-infested sites; most southern site is numbered 1 in both cases with northern sits as 2). Inset is map of Ethiopia with study area marked in rectangle.

2.1.2. Climate

Based on ten years climate data, (2001-2010), the Lake Abaya basin experiences a bimodal rainfall pattern (Figure 2). It has an average annual temperature of 22.9˚C and an average rainfall of 768 mm. The rainy season of the study area ranges from March to November with mean minimum monthly rainfall in January and maximum in May. Hot and dry season is prominent from December to February. The mean minimum daily temperature of the coldest month and the mean maximum temperature of the warmest months are 15.0˚C and 32˚C, respectively.

2.2. Data Collection

For macrophyte sampling, a belt transect was laid along the side of the lake (Figure 1). Samples were collected early mid of September and early January. Four study sites were selected: two water hyacinth-infested and other two sites free from water hyacinth. A picture of the study sites was taken using cannon 10X pixel camera along the western coast of the lake. In each of the four sites 15 plots were laid, each plot (quadrats) with a size of 0.5 × 0.5 m2 and 25 meter apart from each other [12] . In the field, macrophytes were counted within each plot. A total of 60 quadrats 15 from each site were studied. Collected plant specimens were pressed and tagged and taken to Addis Ababa University National Herbarium for identification using the guide to Flora of Ethiopia and Eritrea.

2.3. Data Analyses

Macrophyte species richness, abundance and Simpson’s diversity index, and similarity index for plots was calculated using SPSS version and 17 Multiple

Figure 2. Climate diagram of the study area (from 2001-2010).

Correspondence Analyses with two Dimensions was computed. Correlation of degree of the invasive infestation with species abundance of macrophytes was computed Using Microsoft Excel. Ordination by non-parametric multidimensional scaling and clustering of samplings sites based on macrophyte community composition and abundance was done using Primer (version 6) [13] . Macrophyte plant distribution with respect to plant category was analyzed also using orbit lab software.

Abundance ( A ) = = individualspecies Sampledplots (1)

Proportion ( P ) = individualspecies allindividualsofallspecies (2)

Relativedensity ( R ) = individualspecies allindividualsofallspecies × 100 (3)

Dominance = plotsoccupiedbyaspecies allplots ( m ) (4)

Simpson's index ( D ) = n ( n 1 ) N ( N 1 ) (5)

Evenness = D S (6)

Richness = ( Dmg ) = ( S 1 ) In N (7)

where N = total number of organisms; n = number of particular species; s = total number of spp

Sorensenindex = 2 C A + B (8)

where A―species number in community ‘A’; B―species number in community ‘B’; C―common species number in both communities.

3. Results and Discussion

We recorded a combined total of 23 macrophyte species belonging to 15 families in all the sites. Out of these, 16 species were observed in the water hyacinth-infested sites whereas 17 were observed in the non-infested sites. Thirteen of the 15 families recorded at Lake Abaya were monospecific, only two families, Cyperaceae and Poaceae, were represented by more than one species. Cyperaceae dominated in terms of diversity with 6 species followed by Poaceae with four species (Table 1).

Both the infested sites and non-infested sites had a unique combination of macrophyte communities. Presence of seven macrophyte species, i.e. Sagittaria latifoli (Alismaceae), Cyperus esculentus (Cyperaceae), Lemnae equinoctialis (Lemnaceae), Pistia stratoides (Araceae), Polygonum punctatum (Polygonaceae), Potamogeton crispus (Potamogetonaceae), and Spharganium americanum (Sparginaceae), characterized the non-infested sites. These seven species were absent from infested sites.

On the other hand, six other macrophyte species, namely Bacopa monnieri (Scrophulariaceae), Bulbine abyssinica (Aspodelaceae), Eichhornia crassipe (Pontederaceae), Echinochloa rotundiflora (Poaceae), Isoetes sp. (Isoetaceae), Leptochloa difusca (Poaceae) were found only in infested sites. The remaining ten macrophyte species belonging to five families were recorded in both infested and non-infested sites. Of these, with five species in both habitats, the family Cyperaceae seems to flourish under both conditions.

More than half of the macrophyte species at the studied sites in Lake Abaya were emergent, with the remaining 44% comprised of equal proportions of submerged and free floating forms (Figure 3). It was interesting to note that seven of the ten species common to both infested and non-infested sites were emergent macrophytes.

3.1. Species Richness

Our results showed that species richness in infested sites was 80% - 85% of non- infested sites (Table 1). A similar reduction in species richness in plant communities was also reported by [14] .

Eleven species were recorded from each of the two infested sites. E. crassipes dominated site 1 followed by Cynodon plectostachyus and Cypress difformis. Whereas C. diffusa, B. abyssinica and E. rotundiflora had lower abundance than the three species (Table 2). Macrophyte distribution at site 1 was patchy in that though some macrophytes exhibited considerable abundance in some plots, they were rare in most plots. For example, C. plectostachys occurred only in 8 plots whereas E. crassipes was found in all studied 15 plots of site 1.

E. crassipes and Typha latifolia dominated the second infested site―site 2, together contributing over 50% of the observed abundance (Table 2). The species with the broadest occurrence was T. latipholia, with a distribution spanning over nine plots; the remaining nine species had restricted distribution in the studied plots. Isoetes sp. is the most abundant species at the site but its distribution within the site was limited confirming the patchy nature of macrophyte distribution in Lake Abaya.

Figure 3. Relative abundance of macrophytes with respect to plant category.

Table 1. Macrophyte taxa recorded in the four sites of Lake Abaya, Ethiopia. (FF = free floating, Em = emergent, Sm = submerged: + = present, − = absent, Inf = infested site, Noinf = non-infested sites).

Fourteen macrophyte species were recorded at non-infested site 1 (Table 2). C. plectostachyus followed by C. esculentus, and cynodon dactylon were the most abundant macrophytes at this site. Polygonum punctatum and Lemna equinoctialis have good number of individuals but were recorded in less than ten plots. C. lucanusianus, S. americanum and S. latifolia were the least abundant species. Similarly regarding the relative density and dominance, C. plectostachyus, Eleocharis obtusa and Isoetes were at higher rank, respectively, whereas Rhynchospora corymbosa and Sagitaria latifolia were lower.

Non-infested site 2 had 13 species macrophyte species with C. plectostachys, S. corymbosa and C. difformis as the most abundant taxa. On the other hand, R. corymbosa, P. punuctatum and R. corymbosa were the three least abundant species at the site (Table 2). Even though R. corymbosa and S. latifolia seem to have higher abundance value, the relative density and dominance value clearly indicated

Table 2. Distribution profile of encountered macrophyte species in the four sites (for formula of parameters refer to “Data Analysis”.

that they a clearly limited distribution at the site.

As it can be seen from the above result, E. crassipes was the most dominant macrophyte species in the two infested sites. Infested site-2 seems to be most affected by the invasion of E. crassipes, it has the lowest species composition and total number of individuals. Even though the species number is comparable to infested site-1, the total number of individuals is less than observed at infested site-1. The proportion analyses showed that the ratio of water hyacinth over the other macrophytes is 0.43 and 0.38 in infested sites 1 and 2, respectively. This finding also agrees with [15] .

In the present study Pistia stratiodes was observed only in 5 plots of non-infested sites. Arille [16] discussed the reasons how E. crassipes outcompetes other macrophytes like P. stratiodes for available nutrients. Isoetes is a submerged macrophyte which is affected by the amount of available light. Most likely the thick mat growth of E. crassipes in sites-1 and 2 affected the growth of Isoetes. This species had higher abundance in non-infested site-1 where there was no shading influence. It is understandable that submerged plants would be more prone to the effect of shading than emergent macrophytes [17] . Our current study confirmed this general notion: the abundance of emergent macrophytes was more than twice that of the submerged ones (Figure 3).

At infested site 2, T. latifolia had a comparable number of individuals and seems to co-exist with the dominant invasive species (Figure 4). Tellez et al. [18] indicated that T. latifolia is a beneficial plant for the alien species as mechanical supporter during early growth stage. On the other hand, C. plectostachys is possibly competing with E. crassipes with a clear suppression by the latter when they occur together. For instance, at infested site-1 the number of individual plants of C. plectostachys was 19 whereas that of E. crassipes was 75 individuals (Table 2), but in non-infested site-1 the number of C. plectostachys was much higher, i.e. 65, in the absence of the invasive species (Table 2). However, in infested site-2 the number of E. crassipes was reduced by half in the presence of only 5 individuals of C. plectostachys (Table 2). At the proximate non-infested site-2 C. plectostachys seems to recover to 31 individuals in the absence water hyacinth (Table 2).

The number of macrophyte species in the community showed significant but negative correlation at (r = 0.904 Pearson correlation) (Figure 5). As the number of water hyacinth per plot increases the total number of other macrophyte species in the site decreased. This shows that E. crassipess has serious impact on floral diversity. Arille [16] and [18] reported a similar species reduction when invasive species colonize wetlands. Also, Gichugi [17] and Shibu [5] showed, the

Figure 4. Eichornia crassipes (water hyacinth) infestation in Lake Abaya, Ethiopia.

Figure 5. Correlation of the number of observed macrophyte species per plot against the density of water hyacinth in Lake Abaya, Ethiopia.

former in Africa lake environment, that the invasion of water hyacinth and other related alien species affect the abundance and diversity of macrophytes resulting in largely monotypic floral community structure.

3.2. Community Structure, Similarity & Diversity

Macrophyte communities of the two non-infested sites are more similar with each other than with any of the two infested sites. Furthermore, the level of similarity among non-infested sites was much higher (60%) than macrophyte communities at the two infested sites (45%) (Table 3, Figure 6(a) & Figure 6(b)). Our data also showed that whether a site was infested or non-infested affected macrophyte composition and similarity than physical proximity of sites.

Species diversity at infested sites was lower than diversity at non-infected sites (Table 4). Furthermore, evenness of macrophyte communities at infested sites was lower than non-infested sites, indicating the drastic impact of invasive water hyacinth on diversity. However, whether the observed community difference at the two infested sites is related to the length of time since first infestation is currently unknown. A clear understanding of time of infestation and direction of invasion certainly will help us understand better the level of impact and direction of impact progression in the context of local environmental conditions. Macrophyte assemblages are indicated to be impacted by competition [20] .

3.3. Implications within Local Context

Our data clearly showed that water hyacinth (E. crassipes) greatly affects the floristic composition, abundance and diversity of Lake Abaya. Despite the fact that many macrophyte species might have been outcompeted by the invasive species, this study also showed that some macrophyte species, for example, members of the Poaceae and Cyperaceae family, have the ability to co-exist with the alien plant and even possibly control its further spread. This could be due to a number of potential factors such as the specific growth habit of the macrophyte taxa, that may potentially make those tolerant species less prone to the shading effects and other forms of competition of water hyacinth.

We recognize that wetland ecosystems, especially shallow freshwater lakes in the tropics, continue to face sustained human infraction because of their close ties with local economies and the livelihood of communities. Nevertheless, despite

Table 3. Sorensen [19] similarity indexes of macrophyte communities the four study sites (beta diversity) at Lake Abaya, Ethiopia.

Table 4. Macrophyte diversity, evenness and richness in the four study sites at Lake Abaya, Ethiopia.

Figure 6. Multivariate analysis of community structure. (a) Non-metric Multidimensional Scaling (MDS) based on Bray-Curtis similarities of macrophyte abundance showing the clear distinction between infested and non-infested sites. Non-infested sites appear to be more similar (60%) that infested sites (45%). (b) Cluster Analysis based on Bray-Curtis similarities using square root transformed data clearly separating macrophyte communities of infested sites from non-infested sites.

their critical economic benefits, freshwater bodies largely remain unexplored in terms of what level of human disturbance tilts their sustainability balance and what level of potential resilience they exhibit towards specific kinds and level of environmental disturbances. Consequently, a comprehensive look at the wider environmental, economic and other impacts of the invasive water hyacinth in Ethiopia is currently not only warranted but overdue.

Water hyacinth has now reached the entire rift valley system and ventured to the largest lake in the country located outside the rift valley―Lake Tana. This has triggered a certain level of local outcry in response to the environmental and economic devastation this invasive species caused in Lake Tana [21] . As a result, researchers are now busy investigating the species where its invasion and impact is deemed critical [22] [21] . These efforts are certainly commendable and encouraging. Studies on this species within the framework of local environmental and social conditions, however, need to go beyond recording status quo of occurrence or impact on fisheries and should be able to develop comprehensive models that predict its temporal invasion expansion patterns within the context of specific water body in question, ecosystem impact and potential disruption.

Invasive macrophytes, apart from their myriad of impacts on non-living anthropocentric values of aquatic habitats, they also impact the living component, i.e. microbial, phytoplankton, zooplankton, benthos, macrophytes, fish and other vertebrates, by modifying the physical and chemical environment. Nonetheless, the impact of water hyacinth on ecological communities is known to be non-linear [23] . Availability of specific nutrients, trophic status of water bodies, dominant food web structure, overall community structure and degree of human impact can affect and direct the specific outcome of invasive species such as water hyacinth [24] [25] .

Dissecting these and fleshing out the damage by invasive species and their proportional contribution to the overall ecosystem level changes will be key in making an informed decision towards how to address the invasion of water hyacinth in the specific Ethiopian lake ecosystems. For example, aquatic invertebrates generally increase associated with water hyacinth invasion. The refuge effect of submerged macrophytes in lakes on enhancing zooplankton communities and the control of phytoplankton has been demonstrated to be positive [26] . In some cases, invasive, submerged macrophyte species have impacted zoobenthos positively but not the zooplankton [27] . The impact on fish communities, however, is not straightforward and depends largely on original community composition and food web structure. Gerard, and Triest [23] stated “the response of fish communities to water hyacinth is highly dependent on the pre-existing fish community, preferred and available fish habitat, food requirements and availability, physical & chemical conditions and, likely although not proven, water hyacinth density”. In addition, “dominant non-native macrophytes may cause significant changes in food web structure of invaded ecosystems” [25] . The impact of an ever-dynamic climate on the macrophyte-phytoplankton productivity balance is also not straight forward and complicates the predictive power of research [28] . All this can be complicated even further by the fact that floating macrophytes in tropical habitats [29] may play key ecological role as a carbon sink―an ecosystem function not in the forefront of concerns in relation to immediate & local human suffering.

Therefore, the need to quantify damage at every level of ecosystem services, impact on human livelihood and disruption of normal human activities cannot be over emphasized. Questions addressing specific environmental conditions in the geographically and limnologically different lakes, Abaya and Tana, for example, would contribute to a better understanding of impact and the development of scalable control measures. Given these generalities, it will be only through critical, systematic, fundamental and comprehensive research that implementable models can be developed that will provide policy makers the needed tools not only to ameliorate the impact on already infested water bodies, but even more to fight the spread of water hyacinth to other uninvaded water bodies through all means including public policy and extensive outreach.

Cite this paper: Mengistu, B. , Unbushe, D. and Abebe, E. (2017) Invasion of Water Hyacinth (Eichhornia crassipes) Is Associated with Decline in Macrophyte Biodiversity in an Ethiopian Rift-Valley Lake—Abaya. Open Journal of Ecology, 7, 667-681. doi: 10.4236/oje.2017.713046.
References

[1]   Lakewatch, F. (2007) A Beginner’s Guide to Water Management. University of Florida, Gainesville.

[2]   Gopal, B. and Goel, U. (1993) Competition and Allelopathy in Aquatic Plant Communities. The New York Botanical Garden, New York.

[3]   Wang, J., Yu, D., Xiong, W. and Han, Y-Q. (2008) Above- and Belowground Competition between Two Submersed Macrophytes. Hydrobiologia, 607, 113-122.

[4]   Williamson, M. (1999) Invasion. Ecography, 22, 5-12.

[5]   Shibu, J., Hamindel, P., Daizy, R. and Sougata, B. (2013) Invasive Plant Ecology. In; Shibu, J., Hamindel, P. and Daizy, R., Eds., Invasive Plant Ecology, CRC Press, London, 1-6.

[6]   Wright, A. and Purcell, M. (1995) Eichhornia crassipes (Mart.) Solms-Laubach. In: Shepherd, R.C.H., Richardson, R.G. and Groves, R.H., Eds., The Biology of Australian Weeds, R.G. and F.J. Richardson, Melbourne, 111-122.

[7]   Zhang, Y., Zhang, D. and Barrett, C. (2010) Genetic Uniformity Characterizes the Invasive Spread of Water Hyacinth (Eichhornia crassipes), a Clonal Aquatic Plant. Molecular Ecology, 19, 1774-1786.

[8]   Brundu, G., Azzella, MM, Blasi, C., Camarda, I., Iberite, M. and Celesti-Grapow, L. (2013) The Silent Invasion of Eichhornia crassipes (Mart.) Solms. in Italy. Plan Biosystems, 147, 1120-1127.

[9]   Habtamu, K. (2013) Invasive Alien Weed Species Impacts on Biodiversity and Socio-Economic Aspect in Ethiopia: A Review. International Journal of Science and Research, 4, 2319-7064.

[10]   Sileshi, B. (2007) Abaya-Chamo Lakes Physical and Water Resources Characteristics, including Scenarios and Impacts. Catchment and Lake Research, 162-167.

[11]   Arne, D. (2013) A Comparison Regarding the Physicochemical Variables and Zooplankton Community Characteristics of Two Ethiopian Rift Valley Lakes: Lake Chamo and Lake Abaya. KU Leuven, Bracels, 4.

[12]   Schmidt, W. (1965) Distribution of Aquatic Vegetation as Measured by Line Intercept with SCUBA. Ecology, 46, 816-823.

[13]   Clarke, K. and Warwick, R. (2001) Change in Marine Communities: An Approach to Statistical Analysis and Interpretation. 2nd Edition, PRIMER-E Ltd, Plymouth, p. 172.

[14]   Hejda, M., Pysek, P. and Jarusik, V. (2009) Impact of Invasive Plant on the Species Richness, Diversity and Composition of Invaded Communities. Journal of Ecology, 97, 393-403.

[15]   UNEP (2013) Taking the Pulse of the Planet: Connecting Science with Policy. Global Environmental Alert Service.
http://www.unep.org

[16]   Arille, T. (2011) Water Hyacinth (E. crassipes) Invasive Species Profile.
http://depts.washington.edu/oldenlab/wordpress/wp-content/uploads

[17]   Gichugi, J., Omondi, R., Okurut, T., Matano, A., Boera, P., Jembe, T. and Ofulla, A. (2012) Water Hyacinth Eichhorniacrassipes (Mart.) Solms—Laubach Dynamics and Succession in the Nyanza Gulf of Lake Victoria (East Africa): Implications for Water Quality and Biodiversity Conservation. Scientific World Journal, 2012, Article ID: 106429.

[18]   Téllez, T.R., López, E., Granado, G.L., Pérez, E.A., López, R.M. and Guzmán, J.M.S. (2008) The Water Hyacinth, Eichhornia crassipes: An Invasive Plant in the Guadiana River Basin (Spain). Aquatic Invasions, 3, 42-53.

[19]   Sorensen, T.J. (1948) A Method of Establishing Group of Equal Amplitude in Plant Sociology Based on Similarity of Species and Its Application to Analyses of the Vegetation on Danish Commons. I kommission hos E. Munksgaard, 1-34.

[20]   Boschilia, S., Oliveira, E. and Thomaz, S. (2008) Do Aquatic Macrophytes Co-Occur Randomly? An Analysis of Null Models in a Tropical Floodplain. Oecologia, 156, 203-214.
https://doi.org/10.1007/s00442-008-0983-4

[21]   Asmare, E. (2017) Current Trend of Water Hyacinth Expansion and Its Consequence on the Fisheries around North Eastern Part of Lake Tana, Ethiopia. Journal of Biodiversity & Endangered Species, 5, 189.

[22]   Anteneh, W., Dereje, T., Addisalem, A., Abebaw, Z. and Befta, T. (2015) Water Hyacinth Coverage Survey Report on Lake Tana. Bahir Dar.

[23]   Gérard, J. and Triest, T. (2014) The Effect of Phosphorus Reduction and Competition on Invasive Lemnids: Life Traits and Nutrient Uptake. ISRN Botany, 2014, Article ID: 514294.
https://doi.org/10.1155/2014/514294

[24]   Kosten, S., Jeppesen, E., Huszar, V., Mazzeo, S., Van Nes, E., Peeters, V. and Scheffer, M. (2011) Ambiguous Climate Impacts on Competition between Submerged Macrophytes and Phytoplankton in Shallow Lakes. Freshwater Biology, 56, 1540-1553.
https://doi.org/10.1111/j.1365-2427.2011.02593.x

[25]   Lv, D., Fan, M., Kang, Y. and Blanco, K. (2016) Modeling Refuge Effect of Submerged Macrophytes in Lake System. Bulletin of Mathematical Biology, 78, 662-694.
https://doi.org/10.1007/s11538-016-0154-4

[26]   Kovalenko, K. and Dibble, E. (2011) Effects of Invasive Macrophyte on Trophic Diversity and Position of Secondary Consumers. Hydrobiologia, 663, 167-173.
https://doi.org/10.1007/s10750-010-0570-7

[27]   Mastrantuono, L. and Mancinelli, T. (1999) Long-Term Changes of Zoobenthic Fauna and Submerged Vegetation in the Shallow Lake Monterosi (Italy).
http://www.urbanfischer.de/joumals/limno

[28]   Peixoto, R., Marotta, H., Bastviken, D. and Enrich-Prast, A. (2016) Floating Aquatic Macrophytes Can Substantially Offset Open Water CO2 Emissions from Tropical Floodplain. Ecosystems, 19, 724-736.
https://doi.org/10.1007/s10021-016-9964-3

[29]   Villamagna, A. and Murphy, B. (2010) Ecological and Socio-Economic Impacts of Invasive Water Hyacinth (Eichhornia crassipes): A Review. Freshwater Biology, 55, 282-298.
https://doi.org/10.1111/j.1365-2427.2009.02294.x

 
 
Top