This invention pertains to a new and distinct variety of sugarcane.
Sugarcane variety, Saccharum sp., is a giant, thick, perennial grass of the Gramineae family cultivated in tropical, subtropical, and some temperate regions worldwide for its sweet sap, which is a major source of sugar and molasses. Sugarcane is believed to have originated in what is now known as New Guinea.
This new and distinct sugarcane variety, Saccharum sp., demonstrates superior sugarcane rust disease resistance, and early and high sugar/sucrose content and cane yield characteristics as compared to other available sugarcane varieties known to the inventors. A new variety of sugarcane identified as ‘L97-128’ is disclosed having high cane yield, early maturity, high sucrose content, resistance to sugarcane rust disease, and good ratooning ability.
This new and distinct sugarcane variety is identified as ‘L97-128’, and is characterized by its darker greenish-brown stalk.
The file of this patent contains at least one photograph executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
This new variety of sugarcane, identified as ‘L97-128’, originated as a true seedling, produced by a biparental cross (identified by the inventors as ‘XL92-42’ (unpatented)) between the female parent ‘LCP81-10’ (unpatented) and the male parent ‘LCP85-384’ (unpatented). In this form of variety designation, which is well known among sugarcane breeders, the “L” indicates the cross and selection occurred in the sugarcane breeding program in St. Gabriel, La. The “97” indicates the year of assignment of a permanent variety identification, and “128” is a unique number assigned to varieties that year. The cross was made in 1992, in St. Gabriel, La., and this new variety was selected from among the progeny of the cross. Early stage selection among the progeny was done between the years 1992 and 1996. The seedling of ‘L97-128’ was germinated from a “true seed” in January 1993 and transplanted to the field in April 1993. Selection occurred in the first ratoon crop in 1994 from a single stool of sugarcane. Two stalks were cut and transplanted successfully for asexual reproduction. Asexual propagation of the new cultivar by cuttings has shown that the unique features of this new sugarcane are stable and the plant reproduces true to type in successive generations of asexual propagation. Plants described herein were characterized on Aug. 23-24, 2004 at approximately 150-165 days in age from spring emergence. The stalks characterized were from inner rows unexposed to direct sunlight. See S. B. Milligan, et al., “Registration of ‘LCP 85-384’ Sugarcane,” Crop Sci., vol. 34, pp. 819-820 (1994); and K. P. Bischoff, et al., “The Development of New Sugarcane Varieties at the LSU AgCenter,” J. Amer. Soc. Sugar Technol., vol 24, pp. 142-164 (2004).
‘LCP81-10’ never attained commercial status, but has been used as a parent in the sugarcane breeding program in St. Gabriel, La. ‘LCP85-384’ is one of the most widely grown commercial sugarcane varieties in Louisiana, occupying approximately 88% of the acreage devoted to sugarcane in Louisiana in 2003. The male parent exhibits high cane yield, moderately early maturity, and good ratooning ability. ‘L97-128’ was developed to provide a new variety with characteristics similar to ‘LCP85-384’, but with earlier maturity and improved sugarcane rust resistance. ‘L97-128’ is characterized by a darker greenish-brown stalk. The female parent (LCP81-10) exhibits similar high cane yield characteristics to that of ‘L97-128’, but does not possess the early and high sucrose content of its new progeny. See B. L. Legendre, et al., “The 2003 Louisiana Sugarcane Variety Survey,” Sugar Bulletin, vol. 82(9), pp. 22-28 (2004).
Color terminology used herein is in accordance with the MUNSELL® color charts for plant tissue and the MUNSELL® Book of Color for stalk and leaf determination (Munsell Color, Gretag Macbeth LLC, New Windsor, N.Y.). The color descriptions and color illustrations are as nearly true as is reasonably possible. However, it is understood that both color and other phenotypic expressions described herein may vary from plant to plant with differences in growth, environment and cultural conditions, without any change in the genotype of the variety ‘L97-128’.
‘L97-128’ emerges quickly after planting and exhibits an average, mature stalk height (ground level to the top visible dewlap) of 270 cm, as compared to that of ‘LCP85-384’ (222 cm), and ‘LCP81-10’ (217 cm). The average stalk diameter of ‘L97-128’ is 26 mm, as compared to that of ‘LCP85-384’ (22 mm dia) and ‘LCP81-10’ (27 mm dia). Each variety exhibits a cylindrically-shaped internode (fourth internode from ground level) and a glabrous (lacking hair) growth ring having a width of 0.3 mm. The root band of each variety is 0.7 mm wide, glabrous with straight sides, and exhibits unequally distributed rows of irregularly-shaped root primordia having a diameter of between about 0.25 and about 0.50 mm. The root band of ‘L97-128’ exhibits an extensive wax layer, as compared to that of ‘LCP85-384’ (light wax layer), and ‘LCP81-10’ (moderate wax layer). The internodes of ‘L97-128’ are smooth and glabrous with few, if any, corky patches or cracks, and exhibit an average length at the mid-culm of 18.2 cm. The internodes of ‘L97-128’ and ‘LCP81-10’ exhibit a moderate bud furrow, as compared to that of ‘LCP 85-384’, which exhibit no bud furrow. The buds of each variety are located just above the leaf scar, and are raised above the surface of the root band. ‘L97-128’ and ‘LCP81-10’ similarly exhibit a round bud shape (at the fourth node) with a central germ pore, as compared to that of ‘LCP85-384’, which is pentagonal. The bud diameter of both ‘L97-128’ and ‘LCP81-10’ is 7-9 mm, which is larger than that of ‘LCP85-384’. The buds of ‘L97-128’ are 6-7 mm long and yellow [7.5Y (yellow) 7/8], without any wax surfaces. All three varieties exhibit no setaceous or pilose hairs on the buds. See Table 1.
Under normal growing conditions in Louisiana, ‘L97-128’ does not exhibit any flowering. The following flower description was obtained from a 38 L can culture of ‘L97-128’ grown in St. Gabriel, La., on Oct. 4, 2004 (approximately 130-145 days in age from spring emergence). ‘L97-128’ exhibited a cylindrical-shaped inflorescence peduncle, degenerating from the base, having a width and length of approximately 6 mm and 40-50 mm, respectively, and pubescence throughout, with short, appressed, silvery pilose hairs [R (red)-Y (yellow) 9/10Y (yellow)]. ‘L97-128’ has a 600-610 mm long inflorescence main axis with some pilose hairs. Primary branches of ‘L97-128’ are 295-320 mm long and exhibit appressed racemose branches. Rachis internodes of ‘L97-128’ are glabrous from the bottom of the main axis, and exhibit a few setaceous hairs towards the apex of the main axis. The apex of ‘L97-128’ is predominantly grooved. Sessile spikelets of ‘L97-128’ are 2.5-3.0 mm long with callus hairs having a length of 9-13 mm and a white color [R (red)-Y (yellow) 9/10Y (yellow)]. The sessile spikelets of ‘L97-128’ are lanceolate, acuminate, and have membranous glumes, lemma with a hyaline scale, and yellow stamens [(Y yellow)-G (green) 3.75Y (yellow)] 1.5-2.0 mm long. Pedicellate spikelets of ‘L97-128’ are ovate, acute, rounded at the base, and 2.5-3.0 mm long. The glumes of the pedicillate spikelets of ‘L97-128’ are membranous; the lemma is hyaline; and the stamens are yellow [Y (yellow)-G (green) 3.75Y (yellow)].
To confirm that ‘L97-128’ was a new variety, controlled tests (e.g., pathogen responses and yield), were conducted in St. Gabriel, La. Fifty-one mechanically harvested, outfield variety trials conducted across south Louisiana involving the replication of ‘LCP85-384’, ‘HoCP85-845’, ‘HoCP91-555’, and ‘HoCP96-540’ were selected for comparison tests with ‘L 97-128’ because of their commercial dominance in the Louisiana sugarcane market. Diseases that commonly affect the growth of sugarcane were selected to test for pathogen responses in all the varieties. ‘LCP81-10’, ‘LCP85-384’, and ‘L97-128’ exhibited similar resistance to sugarcane mosaic and sorghum mosaic viruses. ‘L97-128’ exhibited moderate susceptibility to smut (caused by Ustilago scitaminea Sydow & P. Sydow), unlike ‘LCP81-10’ and ‘LCP85-384’, which both exhibited resistance to smut. ‘L97-128’ and ‘LCP81-10’ similarly exhibited moderate resistance to rust (caused by Puccinia melanocephala H. and P. Sydow), unlike ‘LCP85-384’, which exhibited susceptibility to this disease. ‘LCP81-10’, ‘LCP85-384’, and ‘L97-128’ similarly exhibited resistance to leaf scald (caused by Xanthomonas albilineans Ashby, Dowson), under natural field infection conditions. The effect of yellow leaf syndrome on the yield of ‘L97-128’ and its parents are unknown. Similar to both of its parents and all other sugarcane varieties grown in Louisiana, ‘L97-128’ exhibited significant yield loss in ratoon crops from ratoon stunning disease (caused by Clavibacter xyli subsp. xyli Davis). ‘L97-128’ and ‘LCP85-384’ are both susceptible to the sugarcane borer (caused by Diatraea saccharalis Fabricius) insect pest of sugarcane. The reaction of ‘LCP 81-10’ to sugarcane borer is unknown. Field observations show that ‘L97-128’ is no more susceptible to herbicides commonly used for weed control than ‘LCP85-384’. Sugarcane disease and sugarcane borer ratings of ‘L97-128’, ‘LCP81-10’, and ‘LCP85-384’ are shown in Table 2.
No other formal trials have been conducted to date on ‘L97-128’ for other insect pests. ‘L97-128’ does not appear to show any novel insect resistance.
To determine yield, fifty-one mechanically harvested, outfield variety trials involving the replication of ‘L97-128’, ‘LCP85-384’, ‘HoCP85-845’, ‘HoCP91-555’, and ‘HoCP96-540’ (‘HoCP 96-540’ is a half-sibling of ‘L97-128’, sharing the same male parent ‘LCP85-384’) were conducted between the years 2001 and 2003 and various locations within Louisiana. The varieties were planted in Balwin silty clay loam in St. Mary Parish, Commerce silt loam in Pointe Coupee Parish, Commerce silt loam in St. James Parish, Commerce silt loam in Lafourche Parish, Commerce silt loam in Assumption Parish, Jeanerette silt loam in Iberia Parish, Patout silt loam in St. Martin Parish, Commerce silt loam in St. John the Baptist Parish, and Sharkey clay in Terrebonne Parish. Each block/plot was fertilized with nitrogen, potassium, and phosphorous according to standard farm practices associated with each operation. ‘L97-128’ produced an average fiber content of 12.2% after twenty trials, which was slightly higher than the 11.1% average fiber content produced by ‘LCP85-384’. Data for sugar yield, cane yield, sucrose content, stalk weight, and stalk number are shown in Table 3.
Plant-cane maturity tests were conducted in Chacahoula, La. to compare the percentage of sucrose content per ton of cane of ‘L97-128’, ‘LCP 85-384’, ‘HoCP85-845’, ‘HoCP91-555’, and ‘HoCP96-540’. ‘L 97-128’ demonstrated early maturity and continued to accumulate sucrose throughout the harvest, as shown in Table 4. ‘L97-128’ exhibited an 11.1% higher recoverable sucrose content in the plant-cane crop than ‘LCP85-384’, when harvested in mid-September 2003, as shown in Table 4. ‘L97-128’ exhibited a 32.4% higher recoverable sucrose content than ‘LCP 85-384’ when the first ratoon was harvested in August 2003 as shown in Table 5.
Number | Date | Country | |
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20060150291 P1 | Jul 2006 | US |