Sub-zero cold tolerance of Spartina pectinata (prairie cordgrass) and Miscanthus × giganteus: candidate bioenergy crops for cool temperate climates.

Miscanthus × giganteus grown in cool temperate regions of North America and Europe can exhibit severe mortality in the year after planting, and poor frost tolerance of leaves. Spartina pectinata (prairie cordgrass), a productive C4 perennial grass native to North America, has been suggested as an alternative biofuel feedstock for colder regions; however, its cold tolerance relative to M. × giganteus is uncertain. Here, we compare the cold tolerance thresholds for winter-dormant rhizomes and spring/summer leaves of M. × giganteus and three accessions of S. pectinata. All genotypes were planted at a field site in Ontario, Canada. In November and February, the temperatures corresponding to 50% rhizome mortality (LT(50)) were near -24°C for S. pectinata and -4°C for M. × giganteus. In late April, the LT50 of rhizomes rose to -10°C for S. pectinata but remained near -4°C for M. × giganteus. Twenty percent of the M. × giganteus rhizomes collected in late April were dead while S. pectinata rhizomes showed no signs of winter injury. Photosynthesis and electrolyte leakage measurements in spring and summer demonstrate that S. pectinata leaves have greater frost tolerance in the field. For example, S. pectinata leaves remained viable above -9°C while the mortality threshold was near -5°C for M. × giganteus. These results indicate M. × giganteus will be unsuitable for production in continental interiors of cool-temperate climate zones unless freezing and frost tolerance are improved. By contrast, S. pectinata has the freezing and frost tolerance required for a higher-latitude bioenergy crop.

Chilling and frost tolerance in Miscanthus and Saccharum genotypes bred for cool temperate climates.

Miscanthus hybrids are leading candidates for bioenergy feedstocks in mid to high latitudes of North America and Eurasia, due to high productivity associated with the C4 photosynthetic pathway and their tolerance of cooler conditions. However, as C4 plants, they may lack tolerance of chilling conditions (0-10 °C) and frost, particularly when compared with candidate C3 crops at high latitudes. In higher latitudes, cold tolerance is particularly important if the feedstock is to utilize fully the long, early-season days of May and June. Here, leaf gas exchange and fluorescence are used to assess chilling tolerance of photosynthesis in five Miscanthus hybrids bred for cold tolerance, a complex Saccharum hybrid (energycane), and an upland sugarcane variety with some chilling tolerance. The chilling treatment consisted of transferring warm-grown plants (25/20 °C day/night growth temperatures) to chilling (12/5 °C) conditions for 1 week, followed by assessing recovery after return to warm temperatures. Chilling tolerance was also evaluated in outdoor, spring-grown Miscanthus genotypes before and after a cold front that was punctuated by a frost event. Miscanthus×giganteus was found to be the most chilling-tolerant genotype based on its ability to maintain a high net CO2 assimilation rate (A) during chilling, and recover A to a greater degree following a return to warm conditions. This was associated with increasing its capacity for short-term dark-reversible photoprotective processes (ΦREG) and the proportion of open photosystem II reaction centres (qL) while minimizing photoinactivation (ΦNF). Similarly, in the field, M.×giganteus exhibited a significantly greater A and pre-dawn F v/F m after the cold front compared with the other chilling-sensitive Miscanthus hybrids.

Initial events during the evolution of C4 photosynthesis in C3 species of Flaveria.

The evolution of C4 photosynthesis in many taxa involves the establishment of a two-celled photorespiratory CO2 pump, termed C2 photosynthesis. How C3 species evolved C2 metabolism is critical to understanding the initial phases of C4 plant evolution. To evaluate early events in C4 evolution, we compared leaf anatomy, ultrastructure, and gas-exchange responses of closely related C3 and C2 species of Flaveria, a model genus for C4 evolution. We hypothesized that Flaveria pringlei and Flaveria robusta, two C3 species that are most closely related to the C2 Flaveria species, would show rudimentary characteristics of C2 physiology. Compared with less-related C3 species, bundle sheath (BS) cells of F. pringlei and F. robusta had more mitochondria and chloroplasts, larger mitochondria, and proportionally more of these organelles located along the inner cell periphery. These patterns were similar, although generally less in magnitude, than those observed in the C2 species Flaveria angustifolia and Flaveria sonorensis. In F. pringlei and F. robusta, the CO2 compensation point of photosynthesis was slightly lower than in the less-related C3 species, indicating an increase in photosynthetic efficiency. This could occur because of enhanced refixation of photorespired CO2 by the centripetally positioned organelles in the BS cells. If the phylogenetic positions of F. pringlei and F. robusta reflect ancestral states, these results support a hypothesis that increased numbers of centripetally located organelles initiated a metabolic scavenging of photorespired CO2 within the BS. This could have facilitated the formation of a glycine shuttle between mesophyll and BS cells that characterizes C2 photosynthesis.