ORIGINAL RESEARCH article
Sec. Functional Plant Ecology
Differential Interspecific Adaptation to Abiotic Stress by Plantago Species
- 1Department of Comparative Plant and Fungal Biology, Royal Botanic Gardens, Kew, Richmond, United Kingdom
- 2Department of Earth and Environmental Sciences, University of Pavia, Pavia, Italy
- 3Ecological Sciences, The James Hutton Institute, Dundee, United Kingdom
The success of seed-based conservation and restoration efforts using native plant species is largely determined by ensuring two key life history transitions are accommodated. These are from “seed to germinated seed” and “germinated seed to established seedling.” In turn, optimization of these life history transitions is determined by a “genetic × environmental” interaction and later largely characterized by localized climatic (abiotic) conditions. It is these environmental stress factors that can act as natural selection agents for specific plant–trait combinations, or phenotypes. In turn, such adaptation may also limit a species range. To test the relationship between these two early plant life history stage transitions, “seed to germinated seed” and “germinated seed to established seedling,” the attributes were characterized for two species of Plantago that occupy contrasting environments and since these species have potential for native seed-based habit restoration and conservation. The species were Plantago coronopus (L.), localized at lower and drier altitudes, and Plantago lanceolata (L.), characterized as occupying higher and wetter altitudinal clines. Seeds were collected from 20 accessions of six natural populations spanning four European countries for both P. lanceolata and P. coronopus. Seed germination (G) and seedling establishment (S) data were determined at six temperatures (T) and six water potentials (Ψ), and the data obtained were analyzed using a generalized linear model (GLM). The results indicate that P. coronopus has adapted physiologically to its high-altitude conditions such that seed germination and seedling establishment may be more readily achieved in this cooler environment where water is less limiting. In contrast, the lower θT of P. lanceolata better facilitates more efficient seed germination and seedling establishment in drier and warmer clines of lower altitude. In addition to establishing a genotypic (species) underpin for seed and seedling trait differences observed, the insights gained may also be exploited to best deploy each species in situ for seed-based conservation and restoration efforts.
Land abandonment is one of the major threats to the Mediterranean biodiversity (Myers et al., 2000) and is mainly the result of socioeconomic changes where less productive areas, which are also less accessible due to steep topography and/or poor road conditions, have been particularly badly affected (Loumou and Giourga, 2003; Rühl et al., 2005). In addition, crop monocultures and the intensive use of agrochemicals, which characterize conventional food production systems, leave soils degraded and often bare soils (e.g., olive groves and vineyards) throughout the year, leading to erosive processes and loss of soil nutrients. In semiarid zones where majority of the Mediterranean agro ecosystems are located, restorative agronomic approaches using cover crops (Dazy et al., 2008) would help improve soil function (Dölle and Schmidt, 2009; Moreno-de Las Heras et al., 2009) and help realize a more sustainable system for the long-term (Hobbs and Norton, 1996). One restorative agriculture approach for mainly perennial cropping systems is the reestablishment of wild native or indigenous species using seed-based methodologies. However, the success of deploying wild seed in such restorative efforts demands detailed species- and even ecotype-specific knowledge of seed and seedling traits and their response to local environmental factors (Hernández and Pastor, 2008).
Ambient temperatures and water availability are major factors influencing seed germination and seedling establishment (Finch-Savage and Phelps, 1993; Xu et al., 2014; Cochrane et al., 2015; Dürr et al., 2015; Teixeira et al., 2020). Concerning the former, thermal time models of germination rates in response to temperature may be used to estimate “cardinal temperatures,” which define temperature minima or “base temperature” (Tb), below which seeds will not germinate (Garcia-Huidobro et al., 1982; Gummerson, 1986; Dahal and Bradford, 1994; Hardegree and Van Vactor, 1999). The cardinal temperature approach also identifies the temperature at which germination is optimal (To) and the ceiling temperature when germination is prevented (Tc) (Ellis et al., 1986; Alvarado and Bradford, 2002). The Tb is a critical parameter for predictive modeling of the periods during which seed germination is possible (Trudgill et al., 2005), and seeds produced by a community of any given species can show tight regulation of their Tb (Garcia-Huidobro et al., 1982; Covell et al., 1986; Dahal et al., 1990; Kebreab and Murdoch, 1999). Thus, cardinal temperatures can relate seed germination data to germination and to seedling development to indicate the potential occurrence of mature plants (Alvarado and Bradford, 2002) and fulfillment of ecological niche (that is, the match of a phenotype to specific environmental conditions; c.f., Arnaud, 2015).
Regarding water availability, changes in soil water content affect soil water potential and so may affect water transport to, and germination of, seeds (Guillemin et al., 2013; Teixeira et al., 2020). The base water potential (Ψb) is a critical parameter for use in hydrotime models to predict the germination periods of different species (or ecotypes) in a variety of environmental conditions (Bradford, 1990; Welbaum et al., 1990; Guillemin et al., 2013; Dürr et al., 2015).
In a study conducted to estimate Tb and Ψb parameters of 14 species, Guillemin et al. (2013) reported that the number of potential “germination days” varied little among the climatic years tested but substantially between species. That is, species coexistence appears afforded based on differential ecological niches. In terms of ecological restoration and especially restoration activities, which focus upon the use of native seeds from a range of local species, germination traits and predictive models are especially important since the success of restoration, and species coexistence, may depend on seed germination and seedling establishment (Bischoff et al., 2006).
The genus Plantago (Plantaginaceae) is thought to be an ancient family (Kuiper and Bos, 1992) and is here reported on two common herbaceous ruderal species that tend toward being perennial types: Plantago coronopus with therophyte life form and Plantago lanceolata with therophyte or hemicryptophyte life form. The two species occur widely and appear to lack a strong habitat preference, are found in altitude ranges of 1,100 and 2,300 m, and have distributions spanning Eurasia and occidental Europe, respectively (Castroviejo, 1986–2015). The rosette-forming species are pioneer species of disturbed bare ground (Kuiper and Bos, 1992). Naturally occurring and persistent in the soil seed bank, Plantago species are used for seed-based landscape restoration (Schröder and Prasse, 2013). Particularly, P. lanceolata is frequently used in seed cover crop mixtures (Alvarez-Diaz et al., 2016; González et al., 2017) protecting soil and to control pernicious weed species of farmland, and they are also grazing-tolerant (Lawson et al., 2004). P. coronopus is also widely used on well-drained soils, as it is able to establish well despite the potential reduction in available water compared to other soil types (González et al., 2017).
To test the hypothesis that congeneric species may possess distinct traits as adaptations to abiotic stress, i.e., may occupy different ecological niches, we characterized the seed and seedling traits of 10 accessions for each of the two species that were collected from six regions of four countries. The accessions were localized across an array of different altitudes, latitudes, longitudes, and pedoclimatic environments.
Materials and Methods
Seeds from two species P. coronopus and P. lanceolata were collected from 50 to 200 plants per accession in 2015, totaling 20 accessions in six regions covering four countries: Canary islands (Ci, Spain), Andalucía (An, Spain), Minho and Trás-os-Montes (PT, Portugal), Asturias (As, Spain), Sussex (Eg, United Kingdom), and Provence-Alpes-Côte d’Azur (Fr, France). The accessions were sampled at the time of natural seed dispersal (late-summer, Supplementary Table S1). Upon collection, seed of all accessions were cleaned and kept in a controlled environment [15°C, 15% relative humidity (RH)] until germination experiments were performed.
For each accession, we obtained the climatological conditions by cross-referencing their geographic localities with the WORLDCLIM database (Hijmans et al., 2005) using DIVA-GIS software (Hijmans et al., 2004). With the obtained interpolated climatological data, we calculated the average annual temperature (AT) plus the maximum (Tmax) and minimum (Tmin) temperatures. We also recorded average annual precipitation (AP), the monthly average from November to April [or “winter precipitation” (WP)] and May to October [or “summer precipitation” (SP)], and the sum of the annual precipitation (APsum; Supplementary Table S1). A map of the collecting sites was made using The Environmental Stratification of Europe dataset (QGIS Version 2.10.1; Metzger, 2018) with QGIS software version 2.10 (Open Source Geospatial Foundation Project) (Supplementary Figure S1).
The seed mass of each accession was recorded as the mean of 96 seeds selected randomly and weighed individually with a precision balance (UMT2 d = 0.1 μg, METTLER TOLEDO, Leicester, United Kingdom).
Germination and Seedling Development
Laboratory germination (G) experiments were performed in temperature-controlled incubators (LMS, Sevenoaks, United Kingdom). Seeds were sown on 9-cm-diameter Petri dishes on two layers of filter paper (Whatman® Grade1, Sigma Aldrich, Gillingham, United Kingdom) and saturated with 3.5 ml of sterile Milli-Q® water (Merck Millipore, Watford, United Kingdom) and placed in closed plastic bags to prevent evaporation. Each replicate comprised a single Petri dish containing 50 seeds, and three replicate experiments were performed independently. Germination temperature regimes ranged from 5 to 30°C at 5°C intervals at a constant temperature and a 12-h light/12-h dark photoperiod. Germination was scored twice daily for 5 weeks, and germinated seeds were distinguished by protruded radicles (>1 mm). Germinated seeds were monitored every 3 days to score the date of cotyledon opening and were considered seedlings when the developing shoot meristem was visible and any abnormality was absent (NS). At the end of the test period, seeds that had failed to germinate were cut open and classified by appearance as viable or dead depending of embryo presence/absence (Teixeira et al., 2020).
Germination percentages were calculated, and statistical analyses were undertaken using only viable seed (i.e., total germinated plus ungerminated living seed).
The capacity of the seed to germinate under simulated conditions of water deficit was assessed using polyethylene glycol (PEG) solutions of varying concentrations as osmoticum. These tests were performed in three independent replicate experiments using 3.5 ml of PEG solution ranging from 0 to −1.0 MPa with 0.2-MPa intervals. Seeds were incubated at constant temperature in filter paper-containing Petri dishes (as described above) and at a constant temperature of 15°C. Each solution was prepared in triplicate according to Equation (5) described in Hardegree and Emmerich (1990), Equ. 1 (0.129 [PEG]2 T – 14.0 [PEG]2 – 0.40 [PEG]). Where “T” is the temperature for germination and “PEG” is MW 8,000 (Sigma Aldrich, Gillingham, United Kingdom). The Petri dishes were placed in closed plastic bags; one dish per treatment per experiment. Each Petri dish containing 50 seeds sown was scored daily, and seeds with protruded radicles >1 mm were considered to have completed germination. In order to keep the osmotic solutions at the designated water potential, the germinated seeds were carefully transferred to germination paper in transparent resealable plastic boxes (17 cm × 12 cm × 5 cm), which was moistened with 15 ml of the same osmotic solution. The boxes were also placed inside sealable plastic bags. The growing seedlings (S) were observed every 3 days to score cotyledon opening. As before, and at the end of the test, non-germinated seeds were cut open and classified by appearance as viable or dead depending on embryo presence/absence, germination percentages were calculated, and further statistical analyses (see below) were undertaken only with viable seeds (germinated plus remaining viable).
Statistical tests were performed using R v3.6.2 (R Core Team, 2016). The medians and quartiles of the boxplots were calculated using the R-Basic functions. “Germination rate” (GRT in response to differing temperatures and GRW for different osmotica) was inferred from the reciprocal of the time to 50% germination (t50), which was estimated via a sigmoidal curve fit of the cumulative germination for each dish using the Boltzmann equation (Supplementary Figure S2a). Using the range of constant temperatures of each replicate experiment per accession, they were regressed with a linear model to estimate the “base temperature” at which the germination rate was equal to zero (TbG), and “thermal time” (θTG) was estimated with the reciprocal of the (temperature × 1/t50) slope value (Supplementary Figure S2b). The “seedling rate” (SR) was inferred from the reciprocal of the time until 50% of the germinated seeds had open cotyledons (at the constant temperature). The same procedure was used to estimate the base temperature (Tb), at which the rate of development to the seedling stage (for temperature and osmoticum, SRT and SRW, respectively) was equal to zero (TbG and TbS, respectively). The thermal time for this transition (θTS) was also estimated as already described above. To estimate the base water potential (Ψb) at which the GR was equal to zero and the “hydrotime” (θH; time for transition to seedling stage), a similar procedure to that described above was applied using a range of water potentials (i.e., osmotica) to give estimates of θHG and θHS, respectively (Supplementary Figures S2c,d). To estimate the temperatures and osmotica at which the germination and development to the seedling stage percentages were the highest, data were fitted with quadratic polynomial equations using the Origin software (OriginLab, Northampton, MA, United States). This identified the optimum temperatures for germination (ToG) and for seedlings occurrence (ToS).
The GLM tests for maximum germination and development to the seedling stage were performed using a binomial distribution with logit link function, with species as predictor factor using the maximum likelihood estimation method, Wald Chi-Square statistics, and contrast pairwise species. The GLM tests of the base temperatures, thermal and hydrotime, optimum temperatures, and base water potential were performed using the above method with a normal distribution and the identity link function after normality and homogeneity of the variances checking using the Shapiro–Wilk and Levene tests, respectively. All GLM tests were performed with the SPSS Statistics for Windows software (Version 21.0). Germination rates and normal seedling development rates were tested using the Kruskal–Wallis test, comparing temperature conditions and osmoticum using the SPSS Statistics for Windows software (Version 21.0). The base temperatures and thermal time for germination (TbG and θTG, respectively) were regressed against the base temperatures and thermal times for normal seedling development (TbS and θTS, respectively), the base water potentials and hydrotime for germination (ΨbG and θHG, respectively) were regressed against the base water potential and hydrotime for normal seedling development (ΨbS and θHG, respectively), using linear regression with the mean values of the three replicates for each accession and species using the R basic functions. Base temperatures and water potentials were regressed against thermal and hydrotime, and the TbG, TbS, ΨbG, and ΨbS were regressed against the climate traits Tmin, Tmax, WP, and SP. The two-way ANOVA tests comparing species’ TbG with TbS and ΨbG with ΨbS were performed using the SPSS Statistics for Windows software (Version 21.0). The factor analysis of mixed data (FAMD) was performed using the mean values of the three replicates in each physiological trait and the above-described data for geographical and climate conditions as numerical variables with species and region as categorical variables. All numerical variables were centered and scaled to homogenize high discrepancies. The FAMD was performed using the R FactoMineR package (version 2.0). The Spearman’s rank correlation was performed for individual selected species with the means of the three replicates of all treatments. The double correlation matrix of Spearman’s rank and p-values was produced with the R package corrplot (version 0.84) using the correlation matrix (adjusted for ties) and the exact probabilities values previously calculated with the GenStat software (VSN International, Hemel Hempstead, United Kingdom).
Graph theory, a mathematical object corresponding to a network that recently gained much attention, was used to analyze ecological attributes such as biological interaction webs, gene–protein interrelations, and flower and pollinator interactions (Proulx et al., 2005). The approach considers a set of units, called nodes or vertex, connected by edges where nodes represent a component of the network and edges indicate a relationship between them (Windram and Denby, 2015). The graph network analysis of traits was performed with the significant Spearman’s rank p-values in order to obtain a network graph of physiologic and environmental traits using the significant rho traits, where the significant p values in the graph correspond to the edges and the traits correspond to the nodes in an adjacency matrix. The rho p values of geographical vs. geographical traits and geographical vs. climate traits were excluded from the analysis. The weighted and undirected graph was generated with the R package igraph (version 1.0.1).
Significant differences were observed in the trait parameters between the two species (Table 1). P. coronopus reached an observed germination median of 88% at a temperature of 10°C, the experimental temperature closest to the ToG of 11.5°C, while P. lanceolata reached an observed germination median of 51% at a temperature of 15°C, the experimental temperature closest to the ToG of 14.4°C (Figure 1A and Supplementary Table S3). Across geographical regions, P. coronopus showed similar germination responses to temperature, except the accession from Ci (Supplementary Figure S4f) that showed high germination from 5 to 25°C and from As that showed high germination from 10 to 20°C (Supplementary Figure S4e). P. lanceolata also followed similar temperature responses in most regions, except Eg, which showed the lowest germination across temperatures (Supplementary Figure S5d).
Table 1. Statistical results for the generalized linear model (GLM) tests of the maximum germination (G) and development to the seedling (cotyledon-open) (S) stage performed with the binomial distribution and logit link function with species as a predictor factor using the maximum likelihood estimation method, Wald Chi-Square statistics, and contrast pairwise species.
Figure 1. Seed germination percentages calculated from the total viable sowed seeds and normal seedlings as percentage of all germinated seeds, expressing the relative conversion from seed germination to normal seedlings. The boxplots show the minimum, first quartile, median, third quartile, maximum, and the suspected outliers for the germination and seedlings in temperature conditions (A,B) and germination and normal seedlings in osmoticum (C,D). The boxplot colors represent the different species with 10 accessions each: P. coronopus (white); P. lanceolata (blue).
Normal seedlings showed significant differences between species (Table 1) with a high response to a broad range of temperatures for P. coronopus and a narrower range of temperatures with a high normal seedling response for P. lanceolata near the optimum germination temperature (Figure 1B and Supplementary Figures S3, S4 and Supplementary Table S3).
Final germination for each of the species showed a gradual decrease of germination with decreasing water potentials (Figure 1C). A mild osmotic stress of −0.2 MPa moderately decreased the germination in P. coronopus and P. lanceolata compared with the control (0.0 MPa) by 25% and 18%, respectively, while a water potential of −0.8 MPa almost fully reduced germination in both species (Figure 1C and Supplementary Table S4). The development of normal seedlings in osmotic solutions reflects the result for germination of each species (Figure 1D and Supplementary Figures S3, S4 and Supplementary Table S4), showing significant differences between species (Table 1) with a strong decrease in normal seedling development at −0.4 MPa in P. coronopus when compared with the control. Across geographical regions, the inhibition by osmotic stress on normal seedling development was particularly evident in all P. lanceolata accessions (Supplementary Figure S4).
Germination and Normal Seedling Development Rates
Germination rates and seedling development rates (GRT, SRT) differed between temperatures and osmoticum treatments (GRW, SRW). Contrary to P. coronopus where the GRT and SRT increased steadily from 5 to 30°C (Supplementary Figures S5a,b), P. lanceolata showed a transient increase in GRT, with the fastest germination and seedling development at 20°C. Moderate osmotic stress only slightly decreased P. coronopus GRW, but a strong drop was observed at −0.8 MPa. Normal seedling development rates in osmoticum (SRW) were generally lower than GRW, reaching an SRW of zero at −0.8 MPa for both species (Supplementary Figure S5d).
Base Temperatures, Thermal Times, Base Water Potentials, and Hydrotimes
The germination base temperatures (TbG) showed a small difference for the two species, (P = 0.008) (Table 1) with values of 2.0°C for P. coronopus and 3.0°C for P. lanceolata (Supplementary Table S2). Similarly, base temperatures for normal seedling development (TbS) also differed (P = 0.001) (Table 1). P. coronopus showed a lower TbS (1.7°C) when compared with the TbG (P = 0.005) where P. lanceolata showed similar values (Figure 2A and Supplementary Table S2). Despite this, positive correlations were found for both species between the TbG and the TbS (rho = 0.564, P = 0.022; rho = 0.745, P = 0.004) (Figure 2E). The base water potential for normal seedling development (ΨbS) differed between species (P = 0.037), in contrast with the base water potential for germination (ΨbG) (Table 1). P. coronopus and P. lanceolata showed a ΨbS that was higher than the ΨbG (P = 0.0001) (Figure 2B) with values of −0.8 and −1.0 MPa for the former and −0.7 and −1.1 MPa for the latter species (Supplementary Table S2). Unlike the positive correlations for TbG and TbS, both species did not show significant correlations between ΨbG and ΨbS (Figure 2F). Differences were found in normal seedling development thermal time (θTS) between the species but not for germination thermal time (θTG), although strong positive correlations were observed between these traits in both species (Figure 2G). Differences were found for both germination hydrotime (θHG) and normal seedling development hydrotime (θHS), but only P. coronopus revealed a significant correlation between both traits (Figure 2H). Both species showed a higher θT and θH for normal seedling development than for germination (Figures 2C,D).
Figure 2. Comparison of base temperature, base water potential, thermal time, hydrotime, and respective linear traits correlations for germination and normal seedling development for 10 accessions of P. coronopus (black) and P. lanceolata (blue): (A) – germination base temperature (TbG) and normal seedling development base temperature (TbS); (B) – germination base water potential (ΨbG) and normal seedling development base water potential (ΨbS); (C) – germination thermal time (θTG) and normal seedling development thermal time; (D) – germination hydrotime (θHG) and normal seedling development hydrotime (θHS). Linear regressions of the base temperatures for germination (TbG) against the base temperatures for normal seedling development (TbS) (E), base water potential for germination (ΨbG) against the base water potential for normal seedling development (ΨbS) (F), germination thermal time (θTG) against the normal seedling development thermal time (θTS) (G), and germination hydrotime (θHG) against the normal seedling development hydrotime (θHS) (H). Histograms indicate mean ± SEM of two-way ANOVA test comparing the different traits. Asterisks denote the significant difference of p-values where: **p = 0.01; ****p = 0.0001; ns, non-significant at α = 0.05. The scatterplot colors represent the mean values of three replicates by species accession.
Factor Analysis of Mixed Data
An FAMD for P. coronopus and P. lanceolata was performed using the recorded physiological, geographical, and meteorological traits (Figure 3). The first two dimensions of the FAMD for P. coronopus explained 35.0% and 22.2% of the overall variance and for P. lanceolata 34.1% and 26.7%.
Figure 3. Factor analysis of mixed data (FAMD) analysis with species as categorical variables and physiological traits, provenance climate conditions, and geographical coordinates as continuous variables. (A,C) display the quantitative variables that contribute to the total variance; (B,D) display accessions plotted by color-coded regions for P. coronopus and P. lanceolata, respectively. Each accession name contains a species code, accession number, and the region acronym. The environmental temperatures (Tmax, Tmin, and Ta), environmental precipitation (Ap, Sp, and Wp), geographical coordinates (Alt, Lat, and Long), physiological traits (TbG, TbS, ToG, ToS, ΨbG, ΨbS, θTG, θTS, θHG, and θHS), and seed mass (Sm).
The geographical and climate conditions showed a strong contribution to the overall variation for both species (Figures 3A,C). The individual factor maps showed similar and clear clustering by geographical region in both species (Figures 3B,D). In the FAMD for P. coronopus, the first dimension showed the association of altitude with the base temperature, thermal time, and hydrotime due its high contribution to the variance, but TbS and θHG revealed a strong correlation (up to 0.73) with this dimension. In this species, the second dimension explained the effect of the latitude positively correlated with the optimum temperatures, opposite to θTG that was negatively correlated (Figure 3A). In the FAMD for P. lanceolata, the first dimension showed the optimum temperatures and seed mass similarly affected by climate conditions, particularly summer precipitation. The second dimension showed that thermal times, θTG and θTS, were similarly affected by altitude and TbG and θHG were affected by longitude (Figure 3B).
Correlations of Physiological, Spatial, and Meteorological Traits
At the collecting sites, the climate conditions vary widely, with only 129 mm annual precipitation in the Canary Islands to 1,432 mm in the north of Portugal and 713 mm in the south of England. The mean annual temperatures range from 20°C in the Canary Islands to around 10°C in the north of Spain and the south of England (Supplementary Table S1).
The bivariate correlation rank coefficients allowed the evaluation of significant correlations between climate and geographical traits with physiological traits for P. coronopus and P. lanceolata (Figure 4). P. coronopus showed significant correlations of altitude with base temperatures and hydrotime for both germination and normal seedling development, although only base water potential for germination shows the same correlation. This contrasts with P. lanceolata where only correlations of altitude with the hydrotime for germination and thermal time for germination and normal seedling development were found. In both species, the optimum temperatures (ToG and ToS) were correlated with the latitude, while in P. coronopus (but not P. lanceolata), the latitude was also correlated with the base water potential (ΨbG and ΨbS); in P. lanceolata (but not P. coronopus), latitude showed correlations with base temperatures (TbG and TbS) and with thermal time and hydrotime (θTG and θHG). P. coronopus showed positive correlations of TbG and TbS with environmental temperature traits, while in P. lanceolata, only the TbS showed such significant negative correlations. Surprisingly, the Tmin negatively correlated with P. coronopus θHG (Figure 4). In both species, ToG and ToS correlated with environmental precipitation traits, but only P. coronopus showed positive correlations between precipitation and hydrotime traits and negative correlations of all three precipitation traits with the base temperatures. P. lanceolata showed negative θHG and positive θTS correlations with WP. Contrary to P. coronopus, the ΨbG of P. lanceolata was negatively correlated with all precipitation traits (Figures 4, 5G,H). In both species, the ΨbS showed correlations with environmental temperature traits: in P. coronopus with AT and Tmax and in P. lanceolata with Tmin (Figures 4, 5B). The P. coronopus seed mass (Sm) was correlated negatively with the environmental precipitation values and with ToG and ToS (Figure 4). Meanwhile, P. lanceolata seed mass was positively correlated with SP and AP, as well as with ToG and ToS. A positive correlation for P. lanceolata Sm was also found with latitude, and negative correlations were found with the environmental temperature conditions (Figure 4). The correlation analysis demonstrated clear differences in the strategies of these two Plantago species to cope with environmental conditions.
Figure 4. Spearman’s correlation rank diagonal matrix of the geographical, climatic, and experimental data variables (Supplementary Tables S1, S2) for P. coronopus (lower) and P. lanceolata (upper). Each matrix displays the color-coded correlation coefficients (rho) explained by the lateral and bottom color key. The circle sizes represent the rho values with the exact p-values, shaded if P > 0.05 or if not correlated with physiological traits.
Figure 5. Linear regressions for P. coronopus and P. lanceolata base temperatures (A–D) and base water potentials (E–H) against the climate traits: minimum (Tmin; A,E) and maximum (Tmax; B,F) temperatures; winter (WP; C,G) and summer (SP; D,H) precipitation. For each species, the means of three replicate values of 10 accessions were plotted. In each panel, TbG is displayed by brown open squares and brown dotted regression lines, and TbS by green closed symbols and green solid regression lines. Osmoticum traits show similar representation. Each panel shows the Spearman’s correlation (rho) coefficients and p-values.
Graph Network Analysis
Plantago coronopus and P. lanceolata differed in the established community modules and the connected nodes within and among communities (Figure 6). The network with two P. coronopus community modules highlighted that the base temperature for normal seedling development and the germination hydrotime played a key role due to its higher connectivity degree with other traits. The θHG trait was more affected by precipitation than temperature conditions, whereas TbS was similarly affected by both climacteric traits (Figure 6A). In contrast, P. lanceolata showed that the θHG trait connected only with winter precipitation but not summer precipitation (Figure 6B). P. lanceolata was organized in three community modules, highlighting a key role for the seed mass due to its higher connectivity degree with other traits within and between communities. This trait was shown to be strongly affected by temperature and precipitation associated with both optimum temperatures for germination and seedling development, as became clear also in the correlation analysis. Contrary to P. coronopus, the base temperature for normal seedlings in P. lanceolata was associated with both latitude and longitude, and the germination base water potential was mostly associated with the latitude and precipitation values (Figure 6B). These results underline that in these two species, the physiologic traits responded differently to the environmental stimuli.
Figure 6. Undirected graph network object of the Spearman’s rank correlation p-values of P. coronopus (A) and P. lanceolata (B) species. The nodes (circles) correspond to the variable traits, and the edges (lines) correspond to the significant rho p-values of two variables in the correlation matrix. The amount of nodes connected depends on the number of significant p-values of one variable with all the other variables. The network graph displays edges that are most likely within (black lines) and among (red lines). Node size corresponds to the degree of connections; edge widths correspond to the logarithm of the edge weight of the p-value between the two nodes; module communities (M-shaded) are based on edge betweenness (Newman–Girvan algorithm).
Our results indicated that the two Plantago species exhibited significantly different ecological strategies with clear differences in all analyzed physiologic traits except for thermal time and base water potential for germination (Table 1). P. coronopus showed a seedling base temperature (TbS) lower than the germination (TbG), and in P. lanceolata, the TbS was not dissimilar from the TbG, implying that normal seedling development does not present an arrested transition between radicle protrusion and normal seedling development. However, a dissimilar thermal time (θT) was found for the two species, with lower values for P. coronopus’ θTS and θTG (Supplementary Table S2), suggesting that P. coronopus can germinate and progress seedling development in lower temperature environments than P. lanceolata. Despite a similar range, altitude was correlated negatively with TbG, TbS, and water base (ΨbG) in P. coronopus, but not in P. lanceolata, which suggests functional adaptation of the former species to cold environments. This was supported not only by the positive correlation of TbG and TbS with the environmental Tmin and by the very high seed germination and normal seedling development at 5°C but also the positive correlation in P. lanceolata of thermal times with altitude. Results for P. coronopus contrast with a recent study testing the initial temperature of seed germination (Tb) of 49 species from altitudinal temperate climate, in which Rosbakh and Poschlod (2015) conclude that the Tb is strongly negatively correlated with habitat temperature. Results for P. lanceolata were in line, revealing a Tmin negative correlation but only for TbS (Figure 5). Apparently, P. coronopus displays the capacity for soil emergence before the winter frost at temperature profiles, which match with first autumn precipitations. Though it should be noted that the current study design focuses on intraspecific as opposed to interspecific variations, as such, the geographical/habitat sampling may have an effect on the outcome. Altitude negatively correlated with the Tb of P. coronopus, and the capacity to enable life history transitions at low ambient temperatures could be also explained by the higher precipitation at higher altitude (Figure 4 and Supplementary Table S1). The northern distribution range of P. coronopus was restricted to coastal areas, whereas a frequent inland distribution occurs mainly in southern latitudes (Schat, 1981; Kuiper and Bos, 2012), indicating relatively high frost sensitivity. On the other hand, the species showed a continuous increase of germination rate (GRT) up to 30°C (Supplementary Figures S3a,b), indicating also high temperature tolerance. This result agrees with reported values for winter and summer weed species where the germination rate increases from 10 to 30°C (Steinmaus et al., 2000). P. coronopus demonstrated a Tb that coincides with favorable precipitation events whenever they occur during the “germination” (i.e., sufficiently warm) season, whereas P. lanceolata traits seem more suited for germination only in early autumn when the conditions are favorable – avoiding the later season’s low temperatures, which was corroborated by the positive correlations of Tb with the geographical traits and confirmed by the low germination at 5°C. P. lanceolata fresh seeds revealed a dormancy degree dependent on the ecotype (van Groenendael, 1986), which explains the observed lower germination values at an optimum temperature and reflects unsuitable environmental conditions, when the probability of seedling survival is low. This is in line with reports stating that seedlings, which have sprouted early in the growth season with a consequently longer time for development, have a lower risk of mortality under subsequent adverse environmental factors (Ross and Harper, 1972; Harper and Harper, 1977).
Contrary to the base temperatures, the base water potential for normal seedling development showed a strong increase, suggesting that the normal seedling development is more limited by water deficit than by the temperature stress. Both species showed an expected higher θHS than θHG; however, only P. coronopus showed a positive correlation between the hydrotime for germination and normal seedling development where the θHG seems to be a major trait player. The θH value quantifies the inherent speed of germination, which can vary among species and physiological states being a constant for all seed fractions. Meanwhile, the Ψb threshold values vary among seed lots within a species (Bradford, 2002), indicating that P. coronopus ΨbS is not the limitation trait in water deficit but the ΨbG. This is contrary to P. lanceolata, where the seedling conversion was lower in osmotic stress. Indeed, P. coronopus ΨbS showed a negative correlation with the Tmax, indicating higher adaptation of seedlings to osmotic stress in regions with a higher summer temperature, supported by the positive ΨbS correlations with the latitude and by the germination and normal seedling percentages under mild stress. This contrasts with P. lanceolata that showed a ΨbG preference for higher water availability and ΨbS for mild temperature environments, as indicated by the negative correlations with these environmental traits. A field study comparing P. lanceolata survival in dry and wet site conditions showed that, at dry sites, almost all plants died after a period of drought in the summer of the second year, whereas the wet site had the lowest mortality rate (van Tienderen, 1992). This difference in water stress tolerance for these two species is particularly evident when the conversion from germinated seeds to normal seedlings was observed, with P. coronopus close to 40%, whereas P. lanceolata showed marginal values at −0.6 MPa (Figure 1D).
It was reported that seed mass is positively associated with germination across a variety of environments (Pearson et al., 2002; Kahmen and Poschlod, 2008). A study in the early eighties in the Netherlands reported a decrease of P. lanceolata seed mass from plants grown in dry sites, with the capacity to germinate reduced with decreasing seed sizes, in contrast to wet sites, where plants produced larger seeds that germinated better at lower temperatures and had a lower optimum temperature (van Groenendael, 1986). In agreement, our results revealed that, for this species, seed mass (Sm) increased with summer precipitation (May–October), when the seed development and ripening occurs, and correlated negatively with environmental temperatures, emphasizing that the species preferred lower temperature environments. The observed positive correlation of Sm with the To for germination and normal seedling development and the negative correlation with ΨbG explain the central position of P. lanceolata seed mass in the community module with physiologic traits in the network analysis (Figure 6).
Our results showed clear species-specific minimum temperature and minimum water requirements for germination and seedling development. Geographical and environmental traits highly contributed to seed functional traits, with the base temperature for normal seedling development as the most central trait in P. coronopus and the seed mass associated with similar functional traits in P. lanceolata. These results reveal diverse ecological strategies with species-specific importance for functional traits.
Data Availability Statement
All datasets presented in this study are included in the article/Supplementary Material.
AT, PT, and PI conceptualized the work, analyzed the data, discussed the results, and wrote the manuscript. AT conducted the field sampling and laboratory experiments. All authors contributed to the article and approved the submitted version.
The research leading to these results has received funding from the People Programme (Marie Curie Actions) of the European Union’s Seventh Framework Programme FP7/2007-2013/under REA Grant Agreement Number 607785. The Royal Botanic Gardens, Kew, receives grant-in-aid from DEFRA. The James Hutton Institute was supported by the Rural and Environment Science and Analytical Services (RESAS), a Division of the Scottish Government.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We are grateful to Candido Galvez Ramirez (Semillas Silvestres) and Álvaro Bueno (Jardín Botánico Atlántico) for their valuable assistance in choosing the seed collecting sites. We also thank Matías Hernández González, Stephanie Frischie (Semillas Silvestres), and Eduardo Fernaìndez Pascual (Royal Botanic Gardens, Kew) for their help in seed collecting.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2020.573039/full#supplementary-material
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Keywords: Plantago, seed germination, seedling establishment, abiotic stress, conservation
Citation: Teixeira A, Toorop PE and Iannetta PPM (2020) Differential Interspecific Adaptation to Abiotic Stress by Plantago Species. Front. Plant Sci. 11:573039. doi: 10.3389/fpls.2020.573039
Received: 18 June 2020; Accepted: 05 October 2020;
Published: 05 November 2020.
Edited by:Boris Rewald, University of Natural Resources and Life Sciences, Vienna, Austria
Reviewed by:Péter Török, University of Debrecen, Hungary
Rubén Retuerto, University of Santiago de Compostela, Spain
Copyright © 2020 Teixeira, Toorop and Iannetta. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: António Teixeira, firstname.lastname@example.org
†Present address: António Teixeira, Centre of Molecular and Environmental Biology (CBMA), University of Minho, Braga, Portugal