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Water Stress and Temperature Effects on Germination and Early Seedling Growth of Digitaria Eriantha

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Water Stress and Temperature Effects on Germination and Early Seedling Growth of Digitaria Eriantha Vol. 8(32), pp. 4345-4353, 22 August, 2013 DOI: 10.5897/AJAR11.1802 African Journal of Agricultural ISSN 1991-637X ©2013 Academic Journals Research http://www.academicjournals.org/AJAR Full Length Research Paper Water stress and temperature effects on germination and early seedling growth of Digitaria eriantha Brevedan R. E.1,2, Busso C. A.1,2*, Fioretti M. N.1, Toribio M. B.1, Baioni S. S.1, Torres Y. A.1,2, Fernández O. A.1,2, Giorgetti H. D.3, Bentivegna D.2, Entío J.4, Ithurrart L.1,2, Montenegro O.3, Mujica M. de las M.4, Rodríguez G.3 and Tucat G.1,2 1Department of Agronomía, Universidad Nacional del Sur (UNS), 8000 Bahía Blanca, Argentina. 2CERZOS (CONICET), 8000 Bahía Blanca, Argentina. 3Chacra Experimental de Patagones, Ministerio de Asuntos Agrarios, (8504) Carmen de Patagones, Argentina. 4Facultad de Ciencias Agrarias, Universidad Nacional de La Plata, (1900) La Plata, Argentina. Accepted 15 May, 2013 This study focused on the two major processes critical for plant establishment: Seed germination and seedling survival. We determined the effects of (1) water stress and temperature on the germination, and (2) water stress on early seedling growth of Digitaria eriantha cv ‘Irene’. Seeds harvested in 2007 were used for temperature studies, and those coming from 2006 and 2007 for water stress studies. In 2009, viability decreased by 65.4% from 2006 to 2007. During the first twenty-four hours, germination was more than 50% at constant (30 or 35°C) than alternating (10/30 or 10/35°C) temperatures, although total germination was about 80% for all temperature treatments. Polyethylene glycol 8000 was used to impose water stress conditions. Germination percentages and coefficients of velocity decreased with decreasing water potentials. Early seedling growth was smaller at lower water potentials. D. eriantha cv ‘Irene’ appeared to germinate within a wide range of temperatures, but it varied greatly in germination response to water potentials. Results suggest that this species could be planted in late spring-early summer, when seedbed temperatures are increasing and soil moisture might still be adequate. Key words: Perennial grasses, rangelands, seeds, forage, arid zones, Argentina. INTRODUCTION In the rangelands of central Argentina, warm-season, is almost the only native, warm-season, C4, palatable native perennial grass genotypes palatable to cattle are perennial grass available for livestock grazing (Giorgetti scarce (Busso et al., 2004). These genotypes are the et al., 1997). Need of increasing cattle forage production major food source for these animals, which reject most of during the warm season in rangelands of central the other monocots and dicots that are part of the plant Argentina is thus critical. This could be achieved via community. In rangelands at the south of Buenos Aires perennial grass species introduction into the region Province (e.g., the Chacra Experimental de Patagones, (Anderson, 1980). Success in artificial range seeding Patagones, Argentina (40°39'49,7''S, 62°53'6,4''W; 40 requires knowledge of many parameters, including m.a.s.l.), within the Phytogeographical Province of the optimum temperature and moisture conditions for Monte: Cabrera 1976), Pappophorum vaginatum Buckey germination (Sabo et al., 1979). *Corresponding author. E-mail: [email protected]. Tel: 54-291-4595126/4595102. Fax: 54-291-4595127. 4346 Afr. J. Agric. Res. Digitaria eriantha (Steudel) subsp. eriantha is a C4, germination, especially in arid and semiarid environments palatable perennial grass that was introduced in where favorable conditions of water availability and Argentina from South Africa in 1991 (Di Giambatista et temperature regimes may only occur over short time al., 2010). Rimieri (1997) bred the cv. ‘Irene’ from the periods (Owens and Call, 1985). Germination may be South African cv. ‘Sudafricana’; ‘Irene’ showed a better part of the plant life cycle that requires the highest water adaptation than the subsp. eriantha to the soil and potentials (Brown, 1995). Temperature also appears to climatic conditions of the semiarid regions in Argentina. determine the optimal and minimum water potentials for Besides South Africa (Du Toit, 2000), this species has germination in various species (Brown, 1995). This is why spread worldwide [USA: Sanderson et al. (1999); studies on the effects of water stress and temperature on Australia: Hacker et al., 1993); China and Europe: seed germination and early seedling growth are so http://www.ehow.com/info_8407286_genus-species- important when thinking in introducing a rangeland crabgrass.html)]. It characterizes for its resistance to species, like D. eriantha, in water stress-prone drought, healthiness, high warm-season forage rangelands of northwestern Patagonia, Argentina. This production and adaptability to different soils information is actually lacking and essential for trying to (Dannhauser, 1988). Lavin and Johnsen (1977) increase warm-season forage production for livestock in determined that D. eriantha might attain a rating of rangelands of central Argentina. There is also a paucity excellent under warm and dry conditions at a site with of information describing the germination ecology of this 330 mm annual precipitation. perennial. Periods of water stress and high temperature are In arid and semiarid areas, the occurrence of optimum common in rangelands of northwestern Patagonia during conditions for seed germination can vary within and late spring and summer (Torres et al., 2011). It means among years (Romo and Eddleman, 1988). The greater that D. eriantha could be a good potential species to the water stress conditions, the lower will be the total introduce in rangelands of central Argentina. Although germination, and the time to germination (Brown, 1995). some research has been conducted on D. eriantha in this Some seeds will not germinate even under favorable country (Gargano et al., 2004; Pedranzani et al., 2005), conditions because they are dormant; the need for an no studies have yet addressed the importance of water after-ripening may help to avoid seed germination under potential and temperature on the most sensitive unfavorable climate conditions (Brown, 1995). morphological developmental stages to water stress and Specific hypotheses were that (1) total germination high temperatures during summers: seed germination percentage is similar under constant or alternating and early seedling growth (Brown, 1995). temperatures, (2) coefficients of velocity are higher at Optimum temperatures will shorten the time to constant than alternating temperatures, and (3) seedling germination, and they might occur under momentarily growth is higher at greater than lower water potentials. favorable moisture conditions (Bonvissuto and Busso, Our objectives were to (1) identify germination responses 2007). Fulbright (1988) reported that the warm-season of D. eriantha to various temperatures and water bunchgrass Sorghastrum nutans (L.) Nash appeared to potentials, and (2) determine the effect of water stress on germinate within a similar range of temperatures, but it its initial seedling growth. This information will assist varied in germination responses to water potentials. those charged with developing strategies for reestablishing Several studies showed similar or greater germination and managing degraded, central rangelands of percentages at constant than alternating temperatures in northwestern Patagonia, Argentina. various range perennial grasses (Hylton and Bement, 1961; Young and Evans, 1982; Fernández et al., 1991). For example, Brown (1987) reported that alternating MATERIALS AND METHODS temperatures improved overall germination of the perennial bunchgrass Aristida armata, but there was little Study site variation in the rate of germination with incubation under Characteristics of the study site (the Chacra Experimental de constant temperature. Ellern and Tadmor (1966) and Patagones) where D. eriantha could potentially be introduced Heydecker (1960) stated that speedy germination does follow. Climate is temperate semiarid, with higher precipitations not necessarily have to coincide with high germination during the spring and fall seasons (Giorgetti et al., 2000). Long-term percentages. (1981-2010) annual rainfall is 416.7 mm Figure 1), with a mean annual temperature of 14.6°C, absolute minimum temperature of - Plants are susceptible to water stress throughout their 7.6°C (August), absolute maximum temperature of 43°C (January), life-cycle, but are particularly vulnerable during seed mean annual relative humidity of 60%, and mean annual wind germination, and seedling emergence and early growth speed of 13 km h-1. Long-term (2006-2010) mean monthly diurnal (Brown, 1995; Almansouri et al., 2001). Seedling and nocturnal temperatures, precipitations for various years, and development of S. nutans cvs. ‘Lometa’, ‘Cheyenne’, long-term (1981-2010) mean monthly evapotranspiration are ‘Llano’, ‘Oto’, and ‘Tejas’, for example, decreased linearly presented in Figure 1. Soil is a typical Haplocalcid. Average pH is 7, and depth is not a with decreasing water potential (Fulbright, 1988). Another constraint in the soil profile. The plant community is characterized critical factor in successful plant establishment is time to by an open, shrubby stratum which includes different-quality, Brevedan et al. 4347 (A) (B) Figure 1. (A) Averages during 2006-2010 of mean monthly diurnal and nocturnal soil temperatures at 5 cm soil depth from January to December, and (B) monthly precipitation at
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