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Acta Botanica Brasilica

Print version ISSN 0102-3306On-line version ISSN 1677-941X

Acta Bot. Bras. vol.30 no.1 Belo Horizonte Jan./Mar. 2016

http://dx.doi.org/10.1590/0102-33062015abb0233 

Short Communication

Freeze tolerance differs between two ecotypes of Paspalum vaginatum (Poaceae)

Liliana Teresa Fabbri1  * 

Edmundo Leonardo Ploschuk1 

María Virginia López1 

Pedro Insausti1  2 

Gabriel Hugo Rua1  2 

1Facultad de Agronomía, Universidad de Buenos Aires, Av. San Martín 4453 (C1417DSE), Buenos Aires, Argentina

2Member of "Carrera del Investigador", Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina

ABSTRACT

Morphological and physiological responses to freezing were evaluated in two ecotypes of the perennial turfgrass Paspalum vaginatum. Leaf extension rate, number of active meristems, leaf water potential and net photosynthesis were measured on plants of both a commercial cultivar, 'Sea Isle 2000', and a wild ecotype from the Flooding Pampa grasslands of Argentina. Plants were propagated by cloning, cultivated in pots, and examined during 18 consecutive days under two treatments: a non-frozen control treatment (15.5±7 ºC) and a frozen treatment with two stages: Stage 1 with four hours of freezing stress for 10 nights (-5ºC), and Stage 2 with 12 hours of freezing stress for eight nights (five nights at -5ºC and three nights at -8ºC). After these treatments, plants were returned to the outside environment to evaluate shoot injury and post-freezing recovery. Leaf water potential, net photosynthesis and leaf extension rate were significantly higher in the wild ecotype than in the commercial cultivar. Meristem density was reduced after freezing in both ecotypes, but was more pronounced in the commercial cultivar (98.5%) than in the wild ecotype (80%). Thus, the two ecotypes coming from different environments, exhibited different morphological and physiological responses to exposure to freezing temperatures.

Key words: freezing tolerance; leaf water potential; meristem injury; Paspalum vaginatum; photosynthesis; seashore paspalum; turfgrass

Paspalum vaginatum Sw is one of the most important C4grasses, since it plays different ecological roles and has different uses. It is propagated by cloning during spring and summer through stolons and rhizomes, and is highly recommended for coastal sports fields and golf courses due to its tolerance to multiple sources of abiotic stresses such as salinity, drought, and waterlogging (Duncan & Carrow 2000). Paspalum vaginatum is very useful for dune stabilization and erosion control because its initial establishment is very fast in these environments (Shaw & Allen 2003). However, it may behave as a weed and compete with other native species when it is introduced into natural ecosystems (Campos et al. 2004; Riefner et al. 2010).

Commonly known as 'seashore paspalum', this species is native to tropical and subtropical regions worldwide, between 30-35º N-S latitude (Zuloaga & Morrone 2001). It occupies coastal salt and brackish water marshes and other wet habitats worldwide, and usually occurs in areas subjected to different environmental disturbances (Burkart et al. 1990). Freezing is the principal abiotic stress constraint involved in the geographic distribution of warm season turfgrasses. Freezing tolerance has been reported for few cultivars of P. vaginatum, which have a tolerance range between -4 and -7ºC under field conditions, and between -8 and -9ºC in acclimated plants (Cardona et al. 1997). Therefore, differences in freezing injuries between wild ecotypes would be also expected as a consequence of a genetic adaptation process, although no information is currently available.

The aim of this paper is to compare the effects of freezing on morphological and physiological traits in two ecotypes of P. vaginatum from different geographical origins. Our hypothesis was that both ecotypes differ in morphological and physiological traits when they are growing at temperatures below 0ºC and we predicted that the wild ecotype has better freezing tolerance than the commercial cultivar due to adaptation to its natural environment, subjected to freezing episodes in winter and early spring.

For this purpose an experiment was carried out during spring 2008 using cloned plants of two individuals (genets) with fine-textured leaves from two respective ecotypes of P. vaginatum: (1) a wild ecotype (WEc) collected from the Flooding Pampa grassland (Argentina: Prov. Buenos Aires) and (2) a commercial cultivar (CEc) originated in Florida (USA), patented as 'Sea Isle 2000' by the University of Georgia Research Foundation were cultivated in the experimental garden of the School of Agriculture, University of Buenos Aires, Argentina (34°35'S, 58°29'W).

While the CEc cultivar is only propagated vegetatively, the WEc diploid population probably originated from sexual reproduction as is usual among Paspalumdiploids (Quarín 1992; Echarte & Clausen 1993). Since in this experiment the two collected specimens have different reproductive origins, we used cloned plants in order to prevent intraspecific expression differences and to standardize criteria.

Clones were obtained in May from 16 tillers of each ecotype. All tillers were similar in diameter and stage of development and bore three to four fully expanded leaves. They were placed in volcanic perlite for seven days in order to induce rooting. Then, clones were transferred to plastic pots (30 x 20 x 10 cm depth) containing a mixture of organic soil and sand (9:1 v/v) and established in a glasshouse (16.2 ±5 ºC) during two months in the winter season. Photoperiod, radiation and humidity were not controlled in the glasshouse, and 25% of the total radiation was intercepted by the polyethylene cover (PAR inside the glasshouse: 225±101 mol m2 day-1, averaged over 60 days). In August, plants were grown under outdoor conditions (13±6 ºC) until stolons covered the soil surface (Tab. 1). The experiment began in September and was carried out following a completely randomized design with eight replications per treatment and ecotype (eight rows x four columns). During 18 consecutive days, plants were assigned to two treatments: (1) control plants were maintained outside, where temperatures never dropped below 3ºC and (2) freeze treatment plants were subjected to two consecutive stages (Stage 1 and Stage 2, Tab. 1). During Stage 1 plants were exposed to a short-time freeze stress (STF) for four hours at -5ºC during 10 consecutive nights (cycles) in order to mimic natural spring conditions characterized by night freezing events preceded and followed by warm temperatures. For each cycle, eight pots of each ecotype were re-randomized at the end of a cycle inside a climate chamber (Kent S. A., Four stars tropical freezer, Argentina); and temperature stabilized at -5°C. Following the four hours of freezing exposure, plants were returned to their original location outdoors (13.5±5 ºC) until the onset of the following Stage 1 cycle. Stage 2 was performed during eight consecutive nights (cycles) immediately after completion of Stage 1 following a similar procedure. A long-time freeze stress (LTF) of 12 h per night was added, reaching -5ºC during the first five cycles (15±5 ºC outdoors) and -8ºC for the remaining three cycles (18±5 ºC outdoors).

Table 1. Scheme of processing steps applied to plants under freezing treatment with their respective time-durations. 

Duration Daily time Place Temperature
ACCLIMATION 30 days 24 hs outdoor 13±6 ºC
FREEZE TREATMENT Stage 1: Short-Time Freeze (STF) 10 days 4 hs freezing chamber -5ºC (night)
20 hs outdoor 13.5±5 ºC
FREEZE TREATMENT Stage 2: Long-Time Freeze (LTF) 5 days 12 hs freezing chamber -5ºC (night)
12 hs outdoor 15±4 ºC
3 days 12 hs freezing chamber -8ºC (night)
12 hs outdoor 18±4 ºC
RE-ACCLIMATION 30 days 24 hs outdoor 19.5±6 ºC

In order to evaluate freeze damage and recovery of stolons and rhizomes, a period of 30 days of re-acclimation outdoors (19.5±6 ºC) was applied to freeze treatment plants of both ecotypes. Leaf water potential (l) was measured in each plant (eight per ecotype) on the distally and fully expanded leaf of a stolon using a Schölander-type pressure chamber (Bio-Control, Buenos Aires, Argentina). Simultaneously, net photosynthesis (Pn) was calculated as net CO2 exchange rate using a LI-6200 portable closed system (LI-COR Inc., Lincoln, Nebraska). For each plant, Pn was measured for 30 seconds on a portion of a young expanded leaf placed into a chamber (25x10-5m3), with additional lighting of 1500 µmol m-2s-1 (PPFD) light source (QB1 205LI-670, Quantum Devices Inc., Barneveld, WI). At the beginning of each measurement, concentrations of both carbon dioxide and water vapor did not substantially differ from those of the surrounding environment, and the water vapor concentration was maintained constant by regulation with a desiccant valve. These measurements took place daily at midday on sunny days during the first five days of Stage 1.

Leaf elongation rate was recorded daily in both eight control and eight frozen plants of each ecotype over the last four days of Stage 1. Measurements of leaf length (mm day-1) were carried out early in the morning, using a ruler, on two tillers per plant. The elongation of each leaf was followed since its emergence until the ligule became exposed.

Meristem injury was evaluated above (stolons) and below ground (rhizomes) on a square area of the pots (1x10-2 m2). For this purpose, meristem density (defined as the number of viable meristems per unit area) was estimated at the end of Stage 2, after the 30 day re-acclimation period, in both ecotypes and both treatments. Meristems were considered viable when re-growth was visible at the nodes of all living rhizomes and stolons sampled.

Repeated observations of leaf 1 and Pn were analyzed using a linear mixed model for repeated measures (SAS 1990). Leaf extension rate was analyzed using a one way ANOVA and Tukey test for comparisons between means. Meristem number analysis was performed by a non-parametric Wald-Wolfowitz test using the Infostat software (Di Rienzo et al. 2011). Statistical significance of the adjusted models was P<0.05.

A general decreasing pattern of Pn was observed over time, although with a clear difference between ecotypes due to the effect of freezing (Fig. 1A). In fact, while in WEc plants Pn decreased slightly in both treatments, Pn decreased significantly in CEc plants (93% lower than controls, five days after the onset of Stage 1, P<0.001) under freezing conditions, remaining constant in control plants. Further, at sub-zero temperatures, WEc Pn surpassed CEc (P<0.0004), while in control plants Pnrates did not differ between ecotypes. These patterns clearly revealed a higher tolerance of WEc plants to freezing events, in agreement with reports made on other C4 species which may acclimate their photosynthetic apparatus to survive occasional frosts (Sage & Kubien 2007; Long & Spence 2013; Głowacka et al. 2015). Although differences are certainly attributed to a genotypic adaptation of WEc to the cooler environments of Argentina, further research is needed in order to elucidate if the higher tolerance of WEc is due to a constitutive frost adaptation or a greater ability to develop cold acclimation.

Figure 1. Changes in net photosynthesis (Pn, A) and leaf water potential (1, B) of two Paspalum vaginatum ecotypes growing under control (open symbols) and freeze (closed symbols) treatments. Measurements were taken during the first five days of Stage 1 (except the fourth which was rainy), on clear days under similar photon flux density (PPFD) conditions (c. 1500 µmol m-2 s-1, over 400-700 nm). Results represent the mean of eight plants per ecotype. Vertical bars denote standard errors (SE) and are shown only when larger than symbols. 

In the same way, the patterns of leaf 1 were consistent with those observed for Pn (Fig. 1B). While WEc plants exhibited a similar behavior with respect to treated and control plants between -0.1 and -1.2 MPa, a significant drop to -1.4 MPa was observed in treated CEc plants at day 5 (P<0.001). Control CEc values were similar to those for WEc plants. The results clearly suggest that the sensitivity of Pn after freezing conditions is linked to water deficit. Although water availability was not limiting, a possible explanation is that the exposure of roots to low temperatures could have reduced absorption and root extension, negatively affecting water uptake and hence leaf water potential in a few hours (Yu et al.2006; Taiz & Zeiger 2012). This possibility should be tested in further experiments with plants subjected to different temperature regimes between roots and aerial organs.

Differences in the leaf extension rate between ecotypes and treatments (P=0.0182) were detected. The mean comparison test revealed significantly lower leaf extension rates for CEc plants subjected to freezing. In CEc plants leaf extension was nearly 40% lower under freezing while WEc values were similar to those of WEc and CEc controls (Fig. 2). Meristem density was affected by freezing in both ecotypes and the effects persisted 30 days after the end of Stage 2 (Fig. 3). These values were consistent with the more extreme freezing conditions in Stage 2 (Tab. 1). Finally, these results also corroborated the higher tolerance of the wild ecotype (WEc) in response to an abiotic stress such as freezing. First, WEc plants showed a higher potential of meristem availability even without stress, since meristem density was 30% higher than in CEc control plants (P=0.05). This implies a constitutive advantage of the wild material related to the perspective of surviving under an acute stress period. Second, meristem availability was reduced to 1.5% of the control in CEc frozen plants, which could imply a serious constraint for plant survival after adverse conditions. Alternatively, in WEc frozen plants meristem density was reduced to only 20% of that observed for controls (P<0.001) and was 95% higher than observed in CEc frozen plants, increasing the possibility of survival (Kalbereret al. 2006; Trischuket al. 2006).

Figure 2 Cumulative leaf extension in plants of Paspalum vaginatum grown under control (white columns) and freeze conditions (black columns). Measures are based on the last fully expanded leaf of two tillers per plant during the last four days of Stage 1. Each value shows the mean of eight plants per ecotype. Asterisk (*) indicates statistically significant differences between means (P<0.05). Vertical bars denote SE. 

Figure 3. Final meristem density in Paspalum vaginatum, measured after the end of the re-acclimation period in a delimited area of the pots (1x10-2 m2). Each column shows the mean of eight plants per ecotype growing under control conditions (white columns) and after freeze conditions (black columns). Vertical bars denote SE. Different letters indicate statistically significant differences between ecotypes (P<0.05). 

The present research revealed that both ecotypes of P.vaginatum respond differently in morphological and physiological traits when they are exposed to freezing temperatures. These preliminary results allow us to support the proposed hypothesis that the wild ecotype (WEc) expresses greater tolerance to frost and it is better adapted to freezing temperatures in winter than the commercial ecotype 'Sea Isle 2000'. Thus,Paspalum vaginatum ecotypes coming from natural environments subjected to frequent freezing events would promote the development of tolerant genotypes, favoring the expression of traits necessary to use in transition zones. Further studies will be necessary to determine if the different responses to freezing between genotypes are due to constitutive traits or to different abilities for acclimation.

Acknowledgements

We thank JJ Valla and the staff of the 'Lucien Hauman' Botanical Garden for keeping material under cultivation and RD Tortosa for providing us with the freezer chamber. Material of P. vaginatum 'Sea Isle 2000' was made available thanks to the colaboration of A Lavista Llanos and Vivero 'La Amistad' of Edin S.A. (Argentina: Prov. Buenos Aires, Gral. Rodríguez). This investigation was supported by the grant G-432 of the Buenos Aires University, Argentina.

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Received: September 08, 2015; Accepted: November 18, 2015

* Corresponding author:fabbri@agro.uba.ar

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