Skip to main content

Changes in the functional features of macrophyte communities and driving factors across a 70-year period


Functional homogenisation occurs across many areas and organism groups, thereby seriously affecting biodiversity loss and ecosystem functioning. In this study, we examined how functional features of aquatic macrophytes have changed during a 70-year period at community and species levels in a boreal lake district. At the community level, we examined if aquatic macrophyte communities showed different spatial patterns in functional composition and functional richness in relation to main environmental drivers between the time periods. We also observed each species in functional space to assess if species with certain sets of traits have become more common or rare in the 70-year study period. We found changes in the relationship between functional community composition and the environment. The aquatic macrophyte communities showed different patterns in functional composition between the two time periods, and the main environmental drivers for these changes were partly different. Temporal changes in functional richness were only partially linked to concomitant changes in the environment, while stable factors were more important. Species’ functional traits were not associated with commonness or rarity patterns. Our findings revealed that functional homogenisation has not occurred across these boreal lakes, ranging from small oligotrophic forest lakes to larger lakes affected by human impacts.


The ongoing biodiversity loss due to human actions is an undeniable crisis (IPBES, 2019; IUCN, 2019). Land use changes, habitat degradation and introduction of invasive species to ecosystems are among the main causes of biodiversity loss (IPBES, 2019). One consequence of these anthropogenic changes is biotic homogenisation, a process where ecosystems lose their biological uniqueness, and similarity among communities increases (McKinney & Lockwood, 1999; Olden & Rooney, 2006). Contrary to this process, there is biotic differentiation, where similarity among communities decreases (Olden & Poff, 2003). Both processes are multidimensional, as they cover the loss or gain not only of taxonomic distinctiveness over time but also of functional, genetic (e.g. Olden et al., 2004) and phylogenetic (e.g. Harrison et al., 2018; Liang et al., 2019) distinctiveness. However, most studies have focused only on taxonomic homogenisation and differentiation, while functional and genetic aspects have received less attention (Olden et al., 2018; for definitions, see Table 1).

Table 1 Definitions of the general terms used throughout this paper

The importance of functional traits and niche processes has been acknowledged for a relatively long time (e.g. McGill et al., 2006), but functional similarity and uniqueness have only recently received more attention (e.g. Gámez-Virués et al., 2015; Liang et al. 2019). Functional homogenisation, which refers to a loss of specialised species or entire functional groups (Olden et al., 2004), is directly linked to ecosystem functions and indirectly to ecosystem services through the loss of functional diversity (Clavel et al., 2011). The maintenance of multiple functions in an area thus needs multiple species with a variety of traits. It has been suggested that the decline of specialist species can cause global functional homogenisation (Clavel et al., 2011) and that biotic homogenisation is connected with ecosystem multifunctionality (e.g. Hautier et al., 2018). However, the role of beta diversity in ecosystem functioning is still not clear (Mori et al., 2018), and it is still unclear how functional homogenisation and differentiation are acting at different levels of biotic communities and under different levels of human impacts.

It has been argued that we are heading towards an era called ‘Homogocene’, as many studies have shown that human actions are causing increasing biotic homogenisation in different environments (Olden et al., 2018). As there are several studies showing that homogenisation is particularly strongly acting in aquatic environments (e.g. Rahel, 2002; Petsch, 2016), the term ‘Aquatic Homogocene’ has also been introduced. Studies concerning aquatic homogenisation have focused mainly on fish (e.g. Castaño-Sánchez et al., 2018; Richardson et al., 2018) and macroinvertebrates (e.g. Cook et al., 2018; Zhang et al., 2018b; dos Bertoncin et al., 2019), while other organism groups, such as macrophytes, have received less attention. Studies focusing on the biotic homogenisation of aquatic macrophyte communities have found contradicting results, showing either biotic homogenisation or differentiation (e.g. Lougheed et al., 2008; Johnson & Angeler, 2014; Baastrup-Spohr et al., 2017; Elo et al., 2018; Zhang et al., 2018a). These studies have used different approaches and have examined a variety of diversity measurements. Previous studies have been based on historical datasets and re-sampling the same sites (e.g. Baastrup-Spohr et al., 2017; Zhang et al., 2018a), one time point (e.g. Lougheed et al., 2008; Johnson & Angeler, 2014; Elo et al., 2018) or palaeoecological methods (e.g. Salgado et al., 2018).

Functional traits have been studied to some extent with aquatic macrophytes (e.g. Arthaud et al., 2012; Baattrup-Pedersen et al., 2016). However, these investigations have not been done extensively in a temporal framework. Functional homogenisation and differentiation of aquatic macrophyte communities have received even less attention than taxonomic ones. Only Zhang et al. (2018a) studied functional richness and compositional dissimilarities with aquatic macrophytes from before 1970s to after 2000s, and they found functional differentiation of macrophyte assemblages instead of homogenisation, even though their study area in the Yangtze River floodplain has faced strong human impacts for a long time. Furthermore, to our knowledge, there are no studies of functional changes in aquatic macrophyte communities at the species level.

Our aim was to focus on the issue of functional homogenisation and differentiation by examining if functional features of vascular aquatic macrophytes have changed or remained the same after a period of 70 years in boreal lakes (Fig. 1). To increase understanding of functional patterns and underlying mechanisms, we explored these patterns at the community and species levels. We used data of vascular aquatic macrophytes from 1947–1950 and 2017 based on surveys of the same set of boreal lakes. At the community level, we examined if there has been functional homogenisation or differentiation or no change in functional similarity. Also, at the community level, we examined if aquatic macrophyte communities show different spatial patterns in functional composition in relation to the environment between the two time periods. We also studied if changes in functional richness in time are linked to concomitant changes in the environment. To further understand the changes in community composition, we also ordered each species in functional space to see if species with certain sets of traits become more common or rare in the study period (representing the species level). As human impact has not been very strong in our study area, we predicted that there might not be drastic changes in functional features. However, we hypothesised that (1) different environmental variables explain functional community composition between the decades, (2) changes in functional richness are linked to changes in the environment across decades (e.g. Zhang et al., 2018a) and (3) declining species (i.e. ‘losers’) have different functional traits than increasing (i.e. ‘winners’) or stable species (e.g. Steffen et al., 2013).

Fig. 1

Flow chart showing main questions, methods, results and conclusions. See text and Supplementary material Appendix 4 for detailed method and data descriptions

Materials and methods

Study area

We studied 28 lakes located in the southern boreal zone (Ahti et al., 1968) in Finland, in the Kokemäenjoki drainage basin between the two large lakes Roine and Pyhäjärvi (Fig. 2; Supplementary material Appendix 1). Many of these lakes have brown, humic waters and are situated in small chains of lakes and streams, both features typical of boreal lakes. The elevation among the lakes studied varies from 77 to 131 metres above sea level. Nonetheless, changes in environmental conditions occur even along a relatively low elevation gradient in the study area, mainly due to glacial and postglacial processes. Due to these historical processes, fine-grained sediments with nutrients have been washed along the elevational gradient in the landscape, as is common in glaciated areas (Seppälä, 2005). Thus, naturally more eutrophic lakes are located at lower elevations and are mainly surrounded by agricultural land or settlements, while smaller and more oligotrophic lakes at higher elevations in the landscape are less affected by human activity and are surrounded by coniferous forest and peatlands. Key characteristics of these lakes are described in Table 2, and more information of the study area can be found in Lindholm et al. (2019).

Fig. 2

Map showing the location of the study area and the lakes (N = 28) studied. Names of the lakes can be found from Supplementary material Appendix 1

Table 2 Environmental variables, species richness values and descriptive statistic from the 1940s and 2017. Wilcoxon signed rank test results between environmental variables from 1940s and 2017 (N = 28)

Species and trait data

We used aquatic macrophyte data from 28 lakes (Supplementary material Appendix 1) from two different time periods. The first macrophyte survey was conducted in 1947–1951 by Dr. U. Perttula (1954, unpublished), and the second survey was done using similar methods in the summer 2017 (July and August). Two different types of rakes and an aquascope were used in surveying aquatic macrophytes in the whole lake area. In this study, we concentrated on presence-absence data of species classified traditionally as aquatic vascular plants in Finland (Linkola, 1933) and, in addition, from the sedge genus Carex seven tall species that grow in the water. With historical datasets, presence-absence data are usually the most reliable source of information compared to coverage or other information representing abundance in macrophyte studies. We did not include taxa identified to genus level (e.g. Isoëtes sp.) or hybrids in the analysis. However, we combined some species to species complexes due to identification differences between the two decades (Supplementary material Appendix 2). Thus, in total, 65 vascular plant taxa were included (Supplementary material Appendix 2). Species richness values and descriptive statistic in the two decades can be found in Table 2.

To represent functional diversity of aquatic macrophytes, we used four functional traits: growth form, perennation, common method of propagation and potential size (Supplementary material Appendix 2; Lindholm et al. 2019). Growth form division consists of the following classes: ceratophyllid, elodeid, helophyte (incl. tall Carex), isoetid, lemnid and nymphaeid (Toivonen & Huttunen, 1995). Only the main growth form of species was considered. Perennation consisted of three ranked classes: (1) annual, (2) biennial/short lived perennial and (3) perennial. Perennation information was mainly collected from Willby et al.’s (2000) attribute-based data, where some species had an attribute present at two different categories. In such cases, the species obtained a value in between the ranked categories (i.e. 1.5 and 2.5), following Göthe et al. (2017). However, we decided to weight value 2, which indicates the presence of the attribute, at the expense of value 1, which indicates the occasional, but not general exhibition of the attribute. Perennation information was not available in this source for all species, and in such cases, data were complemented by information from other literature sources and databases (e.g. Ecological Database of the British Isles: Degree of vegetative propagation (Klotz et al., 2002) consists of five ranked classes: (1) by seed, (2) mostly by seed but also vegetatively, (3) by seed and vegetatively, (4) mostly vegetatively and also by seed and (5) vegetatively. Potential size information (cm) is a continuous trait from Hämet-Ahti et al. (1998) complemented from Mossberg and Stenberg (2012) for a few species. It represents the potential length of an individual omitting the root or rhizome length (Bornette et al., 1994; Doledec & Statzner, 1994).

Environmental variables

We used the following environmental variables: lake area (ha), elevation (m), maximum depth (m), pH, water transparency (m), land use variables and geographical coordinates of lakes’ centres, as we had only a limited number of environmental variables available from the 1940s (Table 2; Lindholm et al., 2019). Measurements of pH were done in the 1940s in summertime, while in 2017 during the fall overturn. Water transparency (m) was measured using a Secchi disk at the same time as the macrophyte sampling. Land use variables from 200 m buffer zones (Pedersen et al., 2006) were derived from the base maps for both decades (National land survey of Finland, 2017, 2018). We calculated three land use variables proportional to buffer area: agricultural area (i.e. field and pasture area), built area and amounts of ditches. These land use types have changed most over the past decades in the study area. We conducted the Wilcoxon signed rank test to detect differences in environmental variables between 1940s and 2017.

Data analysis

A schematic diagram showing the statistical methodology used can be found in Supplementary material Appendix 3. We did the following analyses to the time periods 1940s and 2017 using the vascular aquatic macrophyte presence-absence data and the functional trait data. All analyses were conducted in the R environment (R Core Team, 2017).

First, to explore functional homogenisation we calculated the amount of functional beta diversity (reflecting both species replacement and loss/gain) among all pairwise comparisons of lakes (Legendre, 2014) for the two time periods separately. We used the Gower distance (Gower, 1971) to calculate between-species distances based on the functional trait data using the function gowdis in the FD package (Laliberté & Legendre, 2010; Laliberté et al., 2014). Then, we used a hierarchical cluster analysis to this species-by-species matrix to produce a trait tree by using the function hclust in the stats package (R Core Team, 2017). Then, using the trait tree and macrophyte presence-absence data (site-by-species matrix), we calculated both the average and the variance of functional beta diversity based on Sørensen dissimilarity index (Legendre & Legendre, 2012) using the function beta.multi in the BAT package (Cardoso et al., 2015, 2018).

Second, we examined if aquatic macrophyte communities showed different spatial patterns among lakes in functional composition in relation to the environment between the 1940s and 2017. We did the following analyses separately for the time periods. We produced a dissimilarity matrix based on the same trait tree and the site-by-species matrix as mentioned above. We generated the functional dissimilarity matrix based on the Sørensen dissimilarity index (Legendre & Legendre, 2012) using the function beta in the BAT package (Cardoso et al., 2015, 2018). Then, we used distance-based redundancy analysis (db-RDA) to examine functional community-environment relationships (Legendre & Anderson, 1999). In this constrained ordination technique, the dissimilarity data are first ordinated using metric multidimensional scaling (principal coordinates analysis, PCoA), and the ordination results are analysed by RDA (Legendre & Anderson, 1999). This method works with any type of distance matrix as the response matrix (Legendre & Legendre, 2012). We selected predictor variables for the model using the forward selection procedure with two stopping rules (Blanchet et al., 2008) using the function ordiR2step in the vegan package (Oksanen, 2017). Then, we ran the db-RDA using the function capscale with the lingoes correction to avoid negative eigenvalues using the vegan package (Oksanen, 2017). Then we tested the model significance by 999 permutations using the function anova in the vegan package (Oksanen, 2017).

Third, we studied how the temporal change in functional richness (i.e. the proportion of the functional space filled by community) is linked to the changes in the environment. As we wanted to measure the total functional range covered by the community (Legras et al., 2018), we used functional richness index (FRic) of Villéger et al. (2008). We calculated FRic based on raw data using the function dbFD with square root correction in the FD package (Laliberté & Legendre, 2010; Laliberté et al., 2014) to each lake for the 1940s and 2017, respectively. Then, we calculated the change in FRic between the two time periods (from now on FRicc). We ran Spearman correlation tests between FRic and species richness in the 1940s and in 2017, and between the FRicc and the change in species richness between decades. We divided our environmental variables to ‘stable’ and ‘non-stable’ variables, as we wanted to find out if changes in FRicc are related to concomitant changes in the environment or environmental factors that are stable through decades. We calculated the change in non-stable environmental variables (pH, water transparency, agricultural area, built area and ditches) between the 1940s and 2017. For clarity, we refer to these changes as pHc, water transparencyc, agricultural areac, built areac and ditchesc. We used values from the 1940s with the more or less stable variables (east and north coordinates, elevation, lake area and depth). Next, we modelled the relationship between FRicc and all environmental variables using linear regression (LR). FRicc was log-transformed to normalise distribution. Collinearity was tested by variance inflation factor (VIF). The LR optimization was based on Akaike’s Information Criterion (AIC) (Burnham & Anderson, 2004).

In addition, we executed commonality analysis to decompose the linear regression R2 to unique and common components of explanatory variables. Unique components indicate how much variance is uniquely accounted for by a single variable, and common components how much variance is common to a variable set. We performed the commonality analysis by using the function commonalityCoefficients in the yhat package (Nimon et al., 2013). To further disentangle the relationship of functional richness to the environment, we examined FRic in the 1940s and 2017 separately. We forced into both LR models four predictor variables based on the previous LR model of FRicc, as the purpose was to compare the same predictor variables between the time periods.

Fourth, we disentangled the changes in macrophyte communities by observing each species in functional space, to see if species with certain sets of traits become more common or rare during the study period. Functional space is a multidimensional space, where the axes are combinations of functional traits and species are placed in the coordinates given by their functional traits (Carmona et al., 2016). We used the Gower distance (Gower, 1971) to calculate between species distances based on the trait data using the function gowdis in the FD package (Laliberté & Legendre, 2010; Laliberté et al., 2014). Then, we used ordination by non-metric multidimensional scaling (NMDS) using the function metaMDS in the vegan package (Oksanen, 2017). In the produced functional space, we plotted species based on NMDS with two dimensions (final stress level = 0.179). We represented the species with different symbols based on whether the species have (1) declined, (2) remained the same (stable) or (3) increased in distribution during the study period in the study area (i.e. differences in the number of localities between two different decades). A species was considered declining when its occurrence decreased by two or more lakes, and vice versa for increasing species. Stable species declined or increased in a maximum of one lake (i.e. from − 1 to 1) between the time periods. Finally, we used permutational multivariate ANOVA (PERMANOVA: Anderson, 2001) to test for significant differences between these three species groups by 999 permutations using the function adonis in the vegan package (Oksanen, 2017). We also associated NMDS species scores to each trait by conducting the Kruskal–Wallis rank sum test (Hollander & Wolfe, 1973) using the function kruskal.test in the stats package (R Core Team, 2017) and by plotting the relationships between the NMSD axes and the four traits.


Changes in environmental variables

The Wilcoxon signed rank test results between the environmental variables from 1940s to 2017 can be found in Table 2. The changes in the non-stable environmental variables from the 1940s to 2017 can be found in Fig. 3. The changes in pH between time periods have been mixed, and the water transparency (m) in the lakes near the urban areas has increased. The lakes where water transparency has declined are located at higher elevations in the landscape, are less affected by human activity and are surrounded by coniferous forest and peatlands. Agricultural area showed a clear declining trend, while built area and ditches have increased in most lake areas (Fig. 3).

Fig. 3

Maps showing the changes in the environmental variables and species richness from the 1940s to 2017 in the lakes (N = 28) studied. Elevation model from National Land Survey of Finland (2015) and water bodies from Finnish Environment Institute (2014)

Functional dissimilarity

There were no clear changes between the 1940s and 2017 in functional beta diversity based on Sørensen dissimilarity index (Fig. 4). The average value of Sørensen dissimilarity index was 0.29 in the 1940s and 0.30 in 2017.

Fig. 4

Variation in functional beta diversity based on Sørensen dissimilarity index in the 1940s and 2017. N = 28 lakes in both 1940s and 2017

Changes in functional community composition

The final db-RDA detected three (P < 0.05) environmental variables related to the variation in functional community composition among the lakes both in the 1940s and 2017 (Fig. 5). In the 1940s, the variables that best accounted for the variation in functional community composition were elevation, depth and ditches. In 2017, pH, depth and area were the most important variables. The amount of explained variation (adj. R2) in both time periods was almost the same, 19.9% in the 1940s and 20.4% in 2017.

Fig. 5

Plots of distance-based redundancy analysis of functional composition of aquatic macrophyte communities in the 1940s (A) and in 2017 (B). The significant environmental variables are shown as arrows in the plots. Names of the lakes can be found from Supplementary material Appendix 1

Changes in functional richness

For the set of traits considered, dimensionality reduction occurred and only the first four PCoA axes were used to calculate FRic for the 1940s. As a result, the quality of the reduced-space representation of FRic was 0.69. For 2017, the first five PCoA axes were used and the quality of the reduced-space representation of FRic was 0.76. FRic in the 1940s was generally higher than in 2017 (Supplementary material Appendix 4, Fig. S1). The Spearman correlation between FRic and species richness in the 1940s was r = 0.92 (P < 0.001) and r = 0.91 (P < 0.001) in 2017. The correlation between the FRicc and the change in species richness between decades was 0.34 (P = 0.075) (Supplementary material Appendix 4, Fig. S2).

The final LR model included only one non-stable variable, agricultural areac, and three stable variables: lake area, elevation and north coordinate (Table 3). The LR model explained 67% of the variation in the change of the FRic (adj. R2 value) and the AIC value was 54.4. The assumptions of normal errors and independency were not statistically violated based on the exploration of residuals, and VIF for all explanatory variables was lower than three. The lakes at the lower elevation in the landscape have had more changes in functional richness between the time points than the lakes in the upper parts of the landscape (Supplementary material Appendix 4, Fig. S3). The size of the lake and the changes in functional richness showed a positive relationship, thus changes in the functional richness are higher in the larger lakes, even though the pattern was not as clear as with elevation. More information about the relationship between FRicc and the change in agricultural area can be found in the Supplementary material Appendix 4 (Figs. S4, S5).

Table 3 Summary of the results of linear regression (LR) analysis (response variable = change in functional richness index between the 1940s and 2017) and commonality analysis for each environmental variable based on linear regression model adjusted R2 values

Based on both the unique and total effects of explanatory variables decomposed from linear regression (R2), elevation contributed the most to the whole LR model. However, the common contribution of elevation to the LR model was higher than the unique, indicating shared effects with the other variables. North coordinate contributed the second most to the whole model based on both the unique and total effects. The only non-stable variable included in the LR model contributed the least based on both the unique and total effects, and the common effect was slightly higher than the unique effect, indicating also shared effects with the other variables (Table 3).

The LR model in the 1940s explained 61% of the variation in the log FRic (adj. R2 value). In the 1940s, the only statistically significant variable was elevation. The LR model in 2017 explained 70% of the variation in the log FRic (adj. R2 value). In 2017, statistically significant variables were agricultural area, lake area and north coordinate (Supplementary material Appendix 4, Table S1).

Species in functional space

For each species in the functional space, there was no clear pattern of species with certain sets of traits becoming more common or rare during the study period (Fig. 6). In addition, based on PERMANOVA, there was no significant difference between the groups of declined, stable or increased species (F = 1.402, 62, P = 0.243). The four traits were significantly different from either one of the NMSD axes based on Kruskal–Wallis rank sum test (Supplementary material Appendix 5).

Fig. 6

Non-metric multidimensional scaling (NMDS) plots of species distribution in functional space. In plot A, shown are species abbreviations (Supplementary material Appendix 2), and in plot B, the lines connect each species to its group centroid. Green = stable species, blue = increased species and grey = decreased species


In many geographical areas and organism groups, the functional homogenisation process has been noticed to occur, thereby seriously affecting ecosystem functioning (e.g. Bergeron et al., 2019). However, we did not find signs of functional homogenisation or, on the other hand, functional differentiation in our study area during a 70-year period for vascular aquatic macrophytes, as the multiple-site functional beta diversity remained almost unchanged. Our prediction that there might not be drastic changes in the functional features was supported, even though we detected some changes. Our hypothesis that different environmental variables would explain the functional community composition between the decades was partly supported. We found that changes have occurred in the functional community composition-environment relationship, as the aquatic macrophyte communities showed different spatial patterns in functional composition between the two time periods, and the main environmental drivers for these changes were partly different. Our second hypothesis that the changes in functional richness would be linked to changes in the environment across decades (e.g. Zhang et al., 2018a) was also partly supported, as we found that changes in functional richness in time were only partially linked to the concomitant changes in the environment. Stable factors, mainly those related to the position of the lakes in the landscape, were more important in explaining the changes in functional richness. Our third hypothesis that declining species (i.e. ‘losers’) would have different functional traits than increasing (i.e. ‘winners’) or stable species did not receive support, as we did not find that species with certain traits would have become more common or rare in the study period.

Changes in the functional composition-environment relationships

Lake depth was the only variable explaining the spatial variation in functional community composition in both 1940s and 2017. It has been found earlier that the relative strength of competitive interactions in a specific functional niche could vary with water depth in macrophyte communities (Fu et al., 2014). In addition, colonisation depth and minimum light requirements vary with macrophyte growth forms (Middelboe & Markager, 1997), which was one of our functional traits. In addition to depth, the functional composition was associated with elevation and the amounts of ditches in the 1940s. In our study area, elevation represents lake landscape position and is temporally a very stable variable. The lake landscape position reflects both the connectivity and lake characteristics (Kratz et al., 1997; Riera et al., 2000), and in our study area, many environmental characteristics are related to this gradient. In other glaciated areas, macrophyte taxonomic community composition has been found to differ along the lake landscape position gradient (Alexander et al., 2008). Thus, it was not a surprise that this gradient was also important to functional composition of vascular macrophyte communities in our study area.

Ecke (2009) found that drainage ditching rather than land use itself could affect water quality and occurrences of macrophytes. However, it was interesting to note that the amounts of ditches were an important variable explicitly in the 1940s, as the amounts of ditches have increased towards 2017 (Fig. 3). It is thus possible that ditching has already had effects on macrophyte communities early on, and further ditching did not have additional impacts. Ditching can affect water chemistry and cause eutrophication in agricultural and urban areas, while in peatland areas it can influence water transparency (Ecke, 2009). In addition, ditches may facilitate the dispersal of aquatic macrophytes by acting as dispersal corridors (Soomers et al., 2010, 2013).

In contrast, in 2017, lake size and pH explained the spatial variation in functional community composition. Larger lakes sustain different functional composition than smaller lakes in our study. Thus, it can be assumed that larger lakes harbour contrasting habitats for biologically and ecologically different macrophyte species, thereby showing functional composition differing from that in small forest lakes. Similar studies on macrophyte communities do not exist to our knowledge, but findings on lake macroinvertebrates have shown that functional composition changes from small to large lakes along with concomitant changes in habitat structural features (Heino, 2008). The importance of pH is different from that of lake size. In acid and neutral waters, increasing pH might first enable the occurrence of different kinds of species causing increases in functional diversity, as high pH is related to increasing levels of bicarbonate and the availability of carbon for macrophytes (Vestergaard & Sand-Jensen, 2000; Iversen et al. 2019). Nonetheless, there is no clear spatial pattern in changes of pH from the 1940s to 2017 (Fig. 3), and based on the Wilcoxon signed rank test, there is no significant change in pH between the decades (Table 2). In addition, it should be taken into account that the pH measurements were done in different seasons, thus limiting the strict comparability between decades.

Patterns and drivers of functional richness

Zhang et al. (2018a) detected a decrease of functional richness of macrophytes in the Yangtze River floodplain, where changes in the environment have been drastic for a long time. We found a similar pattern in functional richness, even though changes in the environment have been only modest in our study area. We also found that the changes in functional richness through time were only partly linked to the concomitant changes in the environment, as stable characteristics of the environment—lake area, elevation and north coordinates—were more prominent than non-stable variables. As elevation in our study area presents the position of the lake in the landscape, it is not a surprise that it was collinear with other explanatory variables. Changes in functional richness were higher in the larger lakes, even though the pattern was not as clear as with elevation. One reason for this could be that, in our study area, the changes in human impact have also been more drastic in the larger lakes.

In our study area, the importance of north coordinate is most likely related to the glaciofluvial deposits and esker formation in the northern part of the study area and the historical development of the lakes nearby. These lakes nearby (e.g. lakes Kaukajärvi (10), Kirkkojärvi (11) and Tohloppi (25) in Fig. 2) are naturally mesotrophic clear-water and spring-fed to some extent. From the non-stable variables, only the changes in agricultural area had impact on changes in functional richness through time. Agriculture is linked to nutrient concentrations, especially total phosphorus (Ecke, 2009) and nitrogen-phosphorus ratios (Arbuckle & Downing, 2001). In our study area, the amount of agricultural area near the lakes has decreased through time, but the relationship with the change in functional richness and the change in agricultural area is not as clear as with elevation.

Traits of ‘losers’ and ‘winners’ through time

At the community level, anthropogenic impacts have been shown to increase the relative abundance of tolerant species with simultaneous decline or loss of specialist species (McKinney & Lockwood, 1999; Olden & Rooney, 2006). This would mean that species with certain sets of traits would become more common (‘winners’) or rare (‘losers’). However, at the species level, we did not find that this pattern had occurred in the study period. One reason for this could be a high intraspecific trait variation with aquatic macrophytes species, as many of them have a high phenotypic plasticity both morphologically and ecologically. A good example for this plasticity is Sagittaria sagittifolia L. (Lacoul & Freedman, 2006), which occurs in our study lakes. Due to plasticity in morphology and physiology, some species can have a different growth form in different environmental conditions (Wetzel, 2001). For example, Eleocharis acicularis (L.) Roem. & Schult. and Ranunculus reptans L. can occur as either helophytes or isoetids. Moreover, Persicaria amphibia (L.) Delarbre can grow either on land or in water (Hutchinson, 1975).

For macrophytes, Fu et al. (2014) found that intraspecific trait variability is an important factor influencing community dynamics and, in addition, intraspecific trait variation has been found to contribute to functional beta diversity patterns (Spasojevic et al., 2016). Therefore, it could be possible that macrophyte species can adapt or adjust to modest changes in the environment. In Germany, aquatic macrophyte species loss in streams has been associated with changes in species traits related to mechanical stress tolerance (Steffen et al., 2013), but the changes in the environment have been more drastic in Central Europe than in our study area in Northern Europe. On the other hand, if one considers the trophic status indicator features of these macrophyte species (Toivonen & Huttunen, 1995), most of the increased macrophytes prefer eutrophic and mesotrophic sites, indicating increasing eutrophication in time in lakes at lower elevations.

Why was functional homogenisation not detected in our study area?

Put together, there are probably four main reasons why we did not find signs of functional homogenisation in our study area during the 70-year study period. First, in our study area, where the changes in the environment have been quite modest, the stable factors in the landscape have a stronger effect than human induced changes on the vascular macrophyte functional composition and the changes in functional richness, thus masking functional homogenisation. Especially, the strong lake landscape position gradient is prominent in our study area. Elo et al. (2018) also did not find signs of biotic homogenisation in relatively oligotrophic lakes in Eastern Finland, where human impact is similarly quite low compared to many other areas worldwide. Second, changes in the environment in relation to human actions have been divergent through time. Urbanisation has intensified in our study area, while the agricultural land area near the lakes has decreased up to the 21st century (Table 2; Fig. 3). Thus, it is possible that these processes are masking the impacts of each other. Generally, in Finland, the use of fertilizers has also increased, while extensive areas of pastures on lakeshores has decreased and the municipal sewer systems have improved. Third, due to high phenotypic plasticity (Lacoul & Freedman, 2006), macrophyte species can probably adapt to these modest changes in the environment. Fourth, as primary producers, macrophytes can have greater landscape-level resilience than consumers (Johnson & Angeler, 2014). Johnson and Angeler (2014) found that macrophyte assemblages did not become homogenised with increased disturbance, although fish and macroinvertebrates did so. It could be argued that there is also a fifth reason. Jarzyna and Jetz (2018) found that temporal functional diversity patterns are scale dependent. Nevertheless, in lake environments, functional diversity patterns should be seen particularly at landscape level (e.g. Heino, 2008), which our study represents. Thus, we do not believe that the issue of spatial scale is a concern in our study. Furthermore, we consider that the time period covered by our study (~ 70 years) is sufficient to observe significant trends in aquatic macrophyte functional changes in case they would exist.


This study increases our knowledge on functional stability of vascular macrophyte communities and driving factors at the landscape level. Even though we did not find signs of functional homogenisation or differentiation, the changes in the environment have affected functional community composition and changes in functional richness to some extent. Thus, the effects of human activity on functional changes of macrophyte communities have probably become more prominent through time. As aquatic macrophytes have a crucial functional and structural role in lake environments, preserving diversity of functional features in aquatic plant communities should be taken into account in land use planning and conservation actions. It is also important to note that these results are based on four specific traits and other patterns could arise with other traits, even though the chosen traits are quite essential, robust and widely used in macrophyte studies. The selection of traits was still to some degree limited because there is a lack of trait information in many cases with more northern and oligotrophic species. Future studies on functional homogenisation should not concentrate only on areas where changes in the environment have been severe, but also on areas where human impact has not been that prominent to help us better understand functional homogenization process in its early stages.


  1. Ahti, T., L. Hämet-Ahti & J. Jalas, 1968. Vegetation zones and their sections in northwestern Europe. Annales Botanici Fennici 5: 169–211.

    Google Scholar 

  2. Alexander, M. L., M. P. Woodford & S. C. Hotchkiss, 2008. Freshwater macrophyte communities in lakes of variable landscape position and development in northern Wisconsin, U.S.A. Aquatic Botany 88: 77–86.

    Google Scholar 

  3. Anderson, M. J., 2001. A new method for non-parametric multivariate analysis of variance. Austral Ecology 26: 32–46.

    Google Scholar 

  4. Arbuckle, K. E. & J. A. Downing, 2001. The influence of watershed land use on lake N: P in a predominantly agricultural landscape. Limnology and Oceanography 46: 970–975.

    Google Scholar 

  5. Arthaud, F., D. Vallod, J. Robin & G. Bornette, 2012. Eutrophication and drought disturbance shape functional diversity and life-history traits of aquatic plants in shallow lakes. Aquatic Sciences 74: 471–481.

    Google Scholar 

  6. Baastrup-Spohr, L., K. Sand-Jensen, S. C. H. Olesen & H. H. Bruun, 2017. Recovery of lake vegetation following reduced eutrophication and acidification. Freshwater Biology 62: 1847–1857.

    CAS  Google Scholar 

  7. Baattrup-Pedersen, A., E. Göthe, T. Riis & M. T. O’Hare, 2016. Functional trait composition of aquatic plants can serve to disentangle multiple interacting stressors in lowland streams. Science of the Total Environment 543: 230–238.

    CAS  PubMed  Google Scholar 

  8. Bergeron, A., C. Lavoie, G. Domon & S. Pellerin, 2019. Changes in spatial structures of plant communities lead to functional homogenization in an urban forest park. Applied Vegetation Science 22: 256–268.

    Google Scholar 

  9. Blanchet, F. G., P. Legendre & D. Borcard, 2008. Forward selection of explanatory variables. Ecology 89: 2623–2632.

    PubMed  Google Scholar 

  10. Bornette, G., C. Henry, M.-H. Barrat & C. Amoros, 1994. Theoretical habitat templets, species traits, and species richness: aquatic macrophytes in the Upper Rhone River and its floodplain. Freshwater Biology 31: 487–505.

    Google Scholar 

  11. Burnham, K. P. & D. R. Anderson, 2004. Multimodel Inference. Sociological Methods & Research 33: 261–304.

    Google Scholar 

  12. Cardoso, P., F. Rigal & J. C. Carvalho, 2015. BAT—Biodiversity Assessment Tools, an R package for the measurement and estimation of alpha and beta taxon, phylogenetic and functional diversity. Methods in Ecology and Evolution 6: 232–236.

    Google Scholar 

  13. Cardoso, P., F. Rigal & J. C. Carvalho, 2018. BAT: Biodiversity Assessment Tools. R package version 1.6.0.

  14. Carmona, C. P., F. de Bello, N. W. H. Mason & J. Lepš, 2016. Traits without borders: integrating functional diversity across scales. Trends in Ecology & Evolution 31: 382–394.

    Google Scholar 

  15. Castaño-Sánchez, A., L. Valencia, J. M. Serrano & J. A. Delgado, 2018. Species introduction and taxonomic homogenization of Spanish freshwater fish fauna in relation to basin size, species richness and dam construction. Journal of Freshwater Ecology Taylor & Francis 33: 347–360.

    Google Scholar 

  16. Clavel, J., R. Julliard & V. Devictor, 2011. Worldwide decline of specialist species: toward a global functional homogenization? Frontiers in Ecology and the Environment 9: 222–228.

    Google Scholar 

  17. Cook, S. C., L. Housley, J. A. Back & R. S. King, 2018. Freshwater eutrophication drives sharp reductions in temporal beta diversity. Ecology 99: 47–56.

    PubMed  Google Scholar 

  18. Doledec, S. & B. Statzner, 1994. Theoretical habitat templets, species traits, and species richness: 548 plant and animal species in the Upper Rhone River and its floodplain. Freshwater Biology 31: 523–538.

    Google Scholar 

  19. dos Bertoncin, A. P., G. D. Pinha, M. T. Baumgartner & R. P. Mormul, 2019. Extreme drought events can promote homogenization of benthic macroinvertebrate assemblages in a floodplain pond in Brazil. Hydrobiologia 826: 379–393.

    Google Scholar 

  20. Ecke, F., 2009. Drainage ditching at the catchment scale affects water quality and macrophyte occurrence in Swedish lakes. Freshwater Biology 54: 119–126.

    CAS  Google Scholar 

  21. Elo, M., J. Alahuhta, A. Kanninen, K. K. Meissner, K. Seppälä & M. Mönkkönen, 2018. Environmental characteristics and anthropogenic impact jointly modify aquatic macrophyte species diversity. Frontiers in Plant Science 9: 1001.

    PubMed  PubMed Central  Google Scholar 

  22. Finnish Environment Institute, 2014. Water formations. CC BY 4.0.

  23. Fu, H., J. Zhong, G. Yuan, P. Xie, L. Guo, X. Zhang, J. Xu, Z. Li, W. Li, M. Zhang, T. Cao & L. Ni, 2014. Trait-based community assembly of aquatic macrophytes along a water depth gradient in a freshwater lake. Freshwater Biology 59: 2462–2471.

    Google Scholar 

  24. Gámez-Virués, S., D. J. Perović, M. M. Gossner, C. Börschig, N. Blüthgen, H. de Jong, N. K. Simons, A.-M. Klein, J. Krauss, G. Maier, C. Scherber, J. Steckel, C. Rothenwöhrer, I. Steffan-Dewenter, C. N. Weiner, W. Weisser, M. Werner, T. Tscharntke & C. Westphal, 2015. Landscape simplification filters species traits and drives biotic homogenization. Nature Communications 6: 8568.

    PubMed  PubMed Central  Google Scholar 

  25. Göthe, E., A. Baattrup-Pedersen, P. Wiberg-Larsen, D. Graeber, E. A. Kristensen & N. Friberg, 2017. Environmental and spatial controls of taxonomic versus trait composition of stream biota. Freshwater Biology 62: 397–413.

    Google Scholar 

  26. Gower, J. C., 1971. A general coefficient of similarity and some of its properties. Biometrics 27: 857–871.

    Google Scholar 

  27. Hämet-Ahti, L., J. Suominen, T. Ulvinen & P. Uotila (eds), 1998. Retkeilykasvio (Field Flora of Finland). Finnish Museum of Natural History, Botanical Museum, Helsinki.

    Google Scholar 

  28. Harrison, T., J. Gibbs & R. Winfree, 2018. Phylogenetic homogenization of bee communities across ecoregions. Global Ecology and Biogeography 27: 1457–1466.

    Google Scholar 

  29. Hautier, Y., F. Isbell, E. T. Borer, E. W. Seabloom, W. S. Harpole, E. M. Lind, A. S. MacDougall, C. J. Stevens, P. B. Adler, J. Alberti, J. D. Bakker, L. A. Brudvig, Y. M. Buckley, M. Cadotte, M. C. Caldeira, E. J. Chaneton, C. Chu, P. Daleo, C. R. Dickman, J. M. Dwyer, A. Eskelinen, P. A. Fay, J. Firn, N. Hagenah, H. Hillebrand, O. Iribarne, K. P. Kirkman, J. M. H. Knops, K. J. La Pierre, R. L. McCulley, J. W. Morgan, M. Pärtel, J. Pascual, J. N. Price, S. M. Prober, A. C. Risch, M. Sankaran, M. Schuetz, R. J. Standish, R. Virtanen, G. M. Wardle, L. Yahdjian & A. Hector, 2018. Local loss and spatial homogenization of plant diversity reduce ecosystem multifunctionality. Nature Ecology & Evolution 2: 50–56.

    Google Scholar 

  30. Heino, J., 2008. Patterns of functional biodiversity and function-environment relationships in lake littoral macroinvertebrates. Limnology and Oceanography 53: 1446–1455.

    Google Scholar 

  31. Heino, J., A. S. Melo & L. M. Bini, 2015. Reconceptualising the beta diversity-environmental heterogeneity relationship in running water systems. Freshwater Biology 60: 223–235.

    Google Scholar 

  32. Hollander, M. & D. A. Wolfe, 1973. Nonparametric Statistical Methods. Wiley, New York.

    Google Scholar 

  33. Hutchinson, G. E., 1975. A treatise on Limnology, Limnological Botany, Vol. 3. Wiley, New York.

    Google Scholar 

  34. IPBES, 2019. Summary for policymakers of the global assessment report on biodiversity and ecosystem services-unedited advance version Members of the management committee who provided guidance for the production of this assessment.

  35. IUCN, 2019. The IUCN Red List of Threatened Species. Version 2019-1.

  36. Iversen, L. L., A. Winkel, L. Båstrup-Spohr, A. B. Hinke, J. Alahuhta, A. Baattrup-Pedersen, S. Birk, P. Brodersen, P. A. Chambers, F. Ecke, T. Feldmann, D. Gebler, J. Heino, T. S. Jespersen, S. J. Moe, T. Riis, L. Sass, O. Vestergaard, S. C. Maberly, K. Sand-Jensen & O. Pedersen, 2019. Catchment properties and the photosynthetic trait composition of freshwater plant communities. Science 366: 878–881.

    CAS  PubMed  Google Scholar 

  37. Jarzyna, M. A. & W. Jetz, 2018. Taxonomic and functional diversity change is scale. Nature Communications 9: 2565.

    PubMed  PubMed Central  Google Scholar 

  38. Johnson, R. K. & D. G. Angeler, 2014. Effects of agricultural land use on stream assemblages: taxon-specific responses of alpha and beta diversity. Ecological Indicators 45: 386–393.

    CAS  Google Scholar 

  39. Klotz, S., I. Kühn & W. Durka, 2002. BIOLFLOR—eine Datenbank mit biologisch-ökologischen Merkmalen zur Flora von Deutschland. Schriftenreihe für Vegetationskunde 38. Bundesamt für Naturschutz, Bonn.

  40. Kratz, T. K., K. E. Webster, C. J. Bowser, J. J. Magnuson & B. J. Benson, 1997. The influence of landscape position on lakes in northern Wisconsin. Freshwater Biology 37: 209–217.

    Google Scholar 

  41. Lacoul, P. & B. Freedman, 2006. Environmental influences on aquatic plants in freshwater ecosystems. Environmental Reviews 14: 89–136.

    Google Scholar 

  42. Laliberté, E. & P. Legendre, 2010. A distance-based framework for measuring functional diversity from multiple traits. Ecology 91: 299–305.

    PubMed  Google Scholar 

  43. Laliberté, E., P. Legendre & B. Shipley, 2014. FD: Measuring functional diversity (FD) from multiple traits, and other tools for functional ecology. R package version 1.0-12.

  44. Legendre, P., 2014. Interpreting the replacement and richness difference components of beta diversity. Global Ecology and Biogeography 23: 1324–1334.

    Google Scholar 

  45. Legendre, P. & M. J. Anderson, 1999. Distance-based redundancy analysis: testing multispecies responses in multifactorial ecological experiments. Ecological Monographs 69: 1–24.

    Google Scholar 

  46. Legendre, P. & L. Legendre, 2012. Numerical Ecology. Elsevier, Amsterdam.

    Google Scholar 

  47. Legras, G., N. Loiseau & J. C. Gaertner, 2018. Functional richness: overview of indices and underlying concepts. Acta Oecologica Elsevier 87: 34–44.

    Google Scholar 

  48. Liang, C., G. Yang, N. Wang, G. Feng, F. Yang, J. C. Svenning & J. Yang, 2019. Taxonomic, phylogenetic and functional homogenization of bird communities due to land use change. Biological Conservation 236: 37–43.

    Google Scholar 

  49. Lindholm, M., J. Alahuhta, J. Heino & H. Toivonen, 2019. No biotic homogenisation across decades but consistent effects of landscape position and pH on macrophyte communities in boreal lakes. Ecography.

    Article  Google Scholar 

  50. Linkola, K., 1933. Regionale Artenstatistik der Süsswasserflora Finnlands. Annales Botanici Societatis Vanamo 3: 3–13.

    Google Scholar 

  51. Lougheed, V. L., M. D. McIntosh, C. A. Parker & R. J. Stevenson, 2008. Wetland degradation leads to homogenization of the biota at local and landscape scales. Freshwater Biology 53: 2402–2413.

    Google Scholar 

  52. Mason, N. W. H., D. Mouillot, W. G. Lee & J. B. Wilson, 2005. Functional richness, functional evenness and functional divergence: the primary components of functional diversity. Oikos 111: 112–118.

    Google Scholar 

  53. McGill, B. J., B. J. Enquist, E. Weiher & M. Westoby, 2006. Rebuilding community ecology from functional traits. Trends in Ecology & Evolution 21: 178–185.

    Google Scholar 

  54. McKinney, M. L. & J. L. Lockwood, 1999. Biotic homogenization: a few winners replacing many losers in the next mass extinction. Trends in Ecology & Evolution 14: 450–453.

    CAS  Google Scholar 

  55. Middelboe, A. L. & S. Markager, 1997. Depth limits and minimum light requirements of freshwater macrophytes. Freshwater Biology 37: 553–568.

    Google Scholar 

  56. Mori, A. S., F. Isbell & R. Seidl, 2018. β-diversity, community assembly, and ecosystem functioning. Trends in Ecology & Evolution 33: 549–564.

    Google Scholar 

  57. Mossberg, B. & L. Stenberg, 2012. Suuri Pohjolan kasvio. Tammi, Helsinki.

    Google Scholar 

  58. National Land Survey of Finland, 2015. Elevation model. CC BY 4.0.

  59. National Land Survey of Finland, 2017. Basic map raster. CC BY 4.0.

  60. National Land Survey of Finland, 2018. Old printed maps. CC BY 4.0.

  61. Nimon, K., F. Oswald & J. K. Roberts, 2013. yhat: Interpreting Regression Effects.

  62. Oksanen, J., 2017. Vegan: ecological diversity. R Package Version 2.4-4 11.

  63. Olden, J. D. & N. L. Poff, 2003. Toward a mechanistic understanding and prediction of biotic homogenization. The American Naturalist 162: 442–460.

    PubMed  Google Scholar 

  64. Olden, J. D. & T. P. Rooney, 2006. On defining and quantifying biotic homogenization. Global Ecology and Biogeography 15: 113–120.

    Google Scholar 

  65. Olden, J. D., N. L. Poff, M. R. Douglas, M. E. Douglas & K. D. Fausch, 2004. Ecological and evolutionary consequences of biotic homogenization. Trends in Ecology & Evolution 19: 18–24.

    Google Scholar 

  66. Olden, J. D., L. Comte & X. Giam, 2018. The homogocene: a research prospectus for the study of biotic homogenisation. NeoBiota 37: 23–36.

    Google Scholar 

  67. Pedersen, O., T. Andersen, K. Ikejima, M. Zakir Hossain & F. Ø. Andersen, 2006. A multidisciplinary approach to understanding the recent and historical occurrence of the freshwater plant, Littorella uniflora. Freshwater Biology 51: 865–877.

    CAS  Google Scholar 

  68. Perttula, U., 1954. Vesi- ja rantakasvien levinneisyydestä ja ekologiasta, eritoten suhtautumisesta veden reaktioon Pirkka-Hämeen limnologisesti erityyppisissä pikku-järvissä (On distribution and ecology of aquatic and shore plants in small lakes in Pirkka-Häme). Unpublished manuscript in Finnish, Dep. Syst. Biol, University of Helsinki.

  69. Petsch, D. K., 2016. Causes and consequences of biotic homogenization in freshwater ecosystems. International Review of Hydrobiology 101: 113–122.

    Google Scholar 

  70. R Core Team, 2017. R: A Language and Environment for Statistical Computing. R Core Team, Vienna.

    Google Scholar 

  71. Rahel, F. J., 2002. Homogenization of freshwater Faunas. Annual Review of Ecology and Systematics 33: 291–315.

    Google Scholar 

  72. Richardson, L. E., N. A. J. Graham, M. S. Pratchett, J. G. Eurich & A. S. Hoey, 2018. Mass coral bleaching causes biotic homogenization of reef fish assemblages. Global Change Biology 24: 3117–3129.

    PubMed  Google Scholar 

  73. Riera, J. L., J. J. Magnuson, T. K. Kratz & K. E. Webster, 2000. A geomorphic template for the analysis of lake districts applied to the Northern Highland Lake District, Wisconsin, U.S.A. Freshwater Biology 43: 301–318.

    Google Scholar 

  74. Salgado, J., C. D. Sayer, S. J. Brooks, T. A. Davidson, B. Goldsmith, I. R. Patmore, A. G. Baker & B. Okamura, 2018. Eutrophication homogenizes shallow lake macrophyte assemblages over space and time. Ecosphere 9: e02406.

    Google Scholar 

  75. Seppälä, M. (ed.), 2005. The Physical Geography of Fennoscandia. Oxford University Press, Oxford.

    Google Scholar 

  76. Soomers, H., D. N. Winkel, Y. Du & M. J. Wassen, 2010. The dispersal and deposition of hydrochorous plant seeds in drainage ditches. Freshwater Biology 55: 2032–2046.

    Google Scholar 

  77. Soomers, H., D. Karssenberg, M. B. Soons, P. A. Verweij, J. T. A. Verhoeven & M. J. Wassen, 2013. Wind and water dispersal of wetland plants across fragmented landscapes. Ecosystems 16: 434–451.

    Google Scholar 

  78. Spasojevic, M. J., B. L. Turner & J. A. Myers, 2016. When does intraspecific trait variation contribute to functional beta-diversity? Journal of Ecology 104: 487–496.

    Google Scholar 

  79. Steffen, K., T. Becker, W. Herr & C. Leuschner, 2013. Diversity loss in the macrophyte vegetation of northwest German streams and rivers between the 1950s and 2010. Hydrobiologia 713: 1–17.

    Google Scholar 

  80. Toivonen, H. & P. Huttunen, 1995. Aquatic macrophytes and ecological gradients in 57 small lakes in southern Finland. Aquatic Botany 51: 197–221.

    Google Scholar 

  81. Vestergaard, O. & K. Sand-Jensen, 2000. Aquatic macrophyte richness in Danish lakes in relation to alkalinity, transparency, and lake area. Canadian Journal of Fisheries and Aquatic Sciences 57: 2022–2031.

    Google Scholar 

  82. Villéger, S., N. W. H. Mason & D. Mouillot, 2008. New multidimensional functional diversity indices for a multifaced framework in functional ecology. Ecology 89: 2290–2301.

    PubMed  Google Scholar 

  83. Violle, C., M. L. Navas, D. Vile, E. Kazakou, C. Fortunel, I. Hummel & E. Garnier, 2007. Let the concept of trait be functional! Oikos 116: 882–892.

    Google Scholar 

  84. Wetzel, R. G., 2001. Limnology: Lake and River Ecosystems. Academic Press, San Diego.

    Google Scholar 

  85. Willby, N. J., V. J. Abernethy & B. O. L. Demars, 2000. Attribute-based classification of European hydrophytes and its relationship to habitat utilization. Freshwater Biology 43: 43–74.

    PubMed  PubMed Central  Google Scholar 

  86. Zhang, M., J. García Molinos, X. Zhang & J. Xu, 2018a. Functional and taxonomic differentiation of macrophyte assemblages across the yangtze river floodplain under human impacts. Frontiers in Plant Science 9: 1–15.

    Google Scholar 

  87. Zhang, Y., L. Cheng, K. Li, L. Zhang, Y. Cai, X. Wang & J. Heino, 2018b. Nutrient enrichment homogenizes taxonomic and functional diversity of benthic macroinvertebrate assemblages in shallow lakes. Limnology and Oceanography 9999: 1–12.

    Google Scholar 

Download references


Open access funding provided by University of Oulu including Oulu University Hospital. We would like to thank Krister Karttunen and all who have participated in the aquatic macrophyte surveys. Jenny and Antti Wihuri Foundation and Olvi Foundation funded the fieldwork in 2017.

Author information




JH, ML and JA designed the study. ML did most statistical analyses, gathered the land use data, and the trait data in part, and wrote the first version of manuscript. ML also participated in the most recent aquatic macrophyte sampling. JA provided the trait data in part. JH contributed to the statistical analysis. HT provided the aquatic macrophyte data and valuable background information, which enabled conducting this study. All authors contributed to writing of the manuscript.

Corresponding author

Correspondence to Marja Lindholm.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Guest editors: André A. Padial, Julian D. Olden & Jean R. S. Vitule / The Aquatic Homogenocene

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 615 kb)

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Lindholm, M., Alahuhta, J., Heino, J. et al. Changes in the functional features of macrophyte communities and driving factors across a 70-year period. Hydrobiologia 847, 3811–3827 (2020).

Download citation


  • Anthropogenic impact
  • Aquatic plants
  • Functional diversity
  • Functional homogenisation
  • Functional richness
  • Temporal patterns