From Scott Haley and Jim Quick, 6/94 (kdk) ====================================================================== About Winter Wheat Data Scott D. Haley Assistant Professor of Plant Science Department of Plant Science South Dakota State University phone: 605-688-4453 email: haleys@mg.sdstate.edu James S. Quick Professor of Agronomy Department of Agronomy Colorado State University phone: 303-491-6483 email: jquick@shep.agsci.colostate.edu ====================================================================== These files contain data collected as part of a research project conducted at Fort Collins, Colorado, during the 1986-1987 growing season. The objectives of the study were to identify variability for various traits related to drought stress tolerance and establish a database for subsequent studies on drought-related traits. Most of the genotypes evaluated represent hard red winter wheats from the Great Plains. Some soft winter wheats and winter durums were also among the germplasm evaluated. NOTE: The data in these files is for informational purposes only. It is not to be used as data for publication nor may it be cited in any published documents. The variables are divided into four separate files: ------------------------------------------------------------ File Name Characteristic Column Header ------------------------------------------------------------ table1.??? Heading HD Anthesis AN Physiological Maturity MAT Grain Filling Duration DUR table2.??? Flag Leaf Width WID Flag Leaf Length LEN Flag Leaf Area LA Specific Leaf Weight SLW table3.??? Flag leaf epicuticular EW/WT wax content (unit dry weight) Flag leaf epicuticular EW/LA wax content (unit area bases) Flag Leaf Stomatal Frequency SF Awn Dry Weight AWN table4.??? Grain Yield GY Grain Volume Weight (Test Weight) TW Kernel Weight KW Plant Height HT ------------------------------------------------------------ ???=xls: Excel V4.0 ???=wk1: Lotus 1-2-3 ???=wq1: Quattro Pro/DOS ???=dbf: dBase III+ ???=txt: tab delimted ASCII text Eighty-one genotypes (cultivars and experimental lines) were planted on 22 September, 1986, in a 9 x 9 partially balanced lattice with four replications. Plot size was six rows, 3.7 meters long, with an inter- row spacing of 0.3 meters. Seeding rates were not adjusted for differences in kernel weight among the entries (40 grams seeded per plot). Sampling for all traits (including mechanical harvest) was done within the central four rows of each plot. Abundant (and evenly distributed) precipitation, coupled with sub-irrigation from a high water table, resulted in extremely luxuriant crop growth and development and exceptionally high average yields. No disease or insect pressures were noted. The following are detailed descriptions of the methods used to measure each trait in the database: Epicuticular Wax Content ------------------------ A gravimetric procedure (D.A. Johnson, USDA-ARS, Logan, Utah, personal communication) was used for flag leaf epicuticular wax (EW) quantification. Plots were sampled at post-anthesis, on 15 June 1987. Duplicate samples of approximately 100 cm2 (estimated by prior LA measurements) of random flag leaves were collected, placed into pre- labeled plastic bags, and transported to the lab. Leaf areas were determined (F87, F88) with an LI-3000 leaf area meter (LI-COR Inc., Lincoln, NE), except at B88 where severe leaf rolling made leaf area measurements impossible. Samples were placed in the freezer to preserve them until EW analysis. For EW extraction, leaf samples were carefully placed with forceps into clean 50 ml beakers. Samples were then washed three times in 15 ml CCl4 (carbon tetrachloride). Total wash time was 40 s for each sample. A teflon repipette was used to dispense the CCl4. The solvent and wax were then filtered through Watman #1 filter paper into clean, dry, 25 x 150 mm test tubes pre-weighed to 0.1 mg with a Mettler H34 analytical balance. After filtering, tubes were suspended in a 75°C water bath to evaporate the solvent. A circulating fan was positioned directly above the tubes to promote evaporation. Once evaporation was complete, tubes were removed from the bath and placed in a 90°C oven. After 24 h the tubes were removed and allowed to come to room temperature. Leaf samples were placed in the oven, at 60°C for 24 h. Cooled tubes and leaf samples were then weighed to 0.1 mg. The wax residue was visible as a tan to yellow solid on the bottom of the tubes. Two blanks per set of 18 tubes (9 plots = 1 block) were also carried through the entire process. To correct for contamination associated with solvent, filtering, or glassware, data were corrected by subtracting the average weight of the two blanks from the net EW weight of each sample. The blank weight typically accounted for less than 5% of the EW yield. EW was calculated from the average of the two samples, reported on both a leaf area (EW/LA; reported in mg m-2) and leaf dry weight (EW/WT; reported in g kg-1) basis. Stomatal Frequency ------------------ Stomatal frequency (SF; reported in number mm-2) was estimated from leaf impressions collected in the field at heading from intact flag leaves. A thin layer of clear cellulose acetate (nail polish) was applied to the middle region of the adaxial surface of two random flag leaves in each plot, taking care to avoid the midrib. This was allowed to dry roughly 5 min and removed with a small piece of clear cellophane tape. Each impression was then applied to a piece of wax paper or plastic transparency for storage. Impressions were examined at 100X on an Olympus BH-2 microscope (Olympus Optical Co., LTD., Tokyo, Japan). Three stomatal counts were recorded per impression, totaling six per plot. Analysis of variance was done on the average of the six samples. Awn Dry Weight -------------- Four random spikes were collected from each plot near maturity and placed in paper bags for awn dry weight measurements (AWN; reported in mg per 20 awns). Twenty awns were clipped (at the tip of the glume) from the central portion of each spike, placed in pollinating bags (smooth surfaced; awns did not stick to the bags), and dried in a 60°C oven for 48 h. Awns were then weighed to 0.1 mg on a Sartorius 1207- MP2 analytical balance (Brinkman Instruments Inc., Westbury, NY). The average of all four samples was used in the analysis. Flag Leaf Area -------------- Flag leaf area (LA; reported in cm2) was determined after heading, following cessation of leaf expansion (Simmons, 1987), in the field on intact flag leaves. Width (WID; reported in mm) and length (LEN; reported in cm) of five randomly selected flag leaves were measured at the broadest portion of the blade and from the auricle to the leaf tip, respectively. Area was then calculated as the product of WID and LEN, multiplied by 0.7 (determined by Fowler and Rasmusson, 1969, as appropriate for barley leaves). The areas were averaged to obtain an estimate of single flag leaf area. Specific Leaf Weight -------------------- Specific leaf weight (SLW; reported in g m-2) was determined using leaf area and leaf dry weight measurements obtained during the EW extraction procedure. Maturity, Duration of Grain Filling, and Yield ---------------------------------------------- The number of days (from January 1) to mean heading (HD) and anthesis (AN) dates were recorded. Mean physiological maturity (MAT) was estimated as the number of days (from January 1) to the appearance of yellow or brown glumes on 50% of the spikes in the plot. Duration of grain filling (DUR) was calculated as the number of days between anthesis and physiological maturity dates (Gebeyehou et al., 1982). Grain yield (GY; reported in g m-2), grain volume weight (test weight, TW; reported in kg m-3), and kernel weight (KW; reported in mg kernel- 1) were obtained following harvest.