At a large, commercial midwestern packing plant, beef carcasses (n = 60) were selected prior to entering the cooler after harvest based upon a 3 × 3 factorial scheme with three levels of carcass weight (thin, medium, and heavy) and three levels of 12th rib external fat depth (thin, average, and fat).
Carcasses were probed with a temperature logger (ThermoWorks THS-294-933, ThermoWorks, American Fork, UT) into the cushion of the round. The probe was angled towards the deep portion of the round and temperature points were recorded every 15 minutes for 24 hours while carcasses were in the chill cooler prior to grading and fabrication.
24 to 36 hours after cooling, carcasses were ribbed, and data was collected by USDA personnel. The data consisted of hot carcass weight (HCW), 12th ribeye area, kidney, pelvic, and heart fat (KPH). Loin pH was measured by NDSU personnel between the 12th and 13th rib before entrance to the carcass cooler, and after 24 hours of chilling.
After grading, carcasses were fabricated into primal cuts. Beef top rounds (Institutional Meat Purchase Specification {IMPS} 169) and top sirloin butts (IMPS 184) were vacuum packaged and transported back to North Dakota State University’s Meats Laboratory. The primal cuts were stored at approximately 35°F for 14 days (sirloins) and 21 days (rounds). Primal cuts were weighed with and without packaging, using the weight differences to calculate the percentage of purge. Each primal cut was measured for external fat depth and fabricated into 1-inch-thick steaks (IMPS 1169 and 1184) for cook loss and Warner-Bratzler shear force analysis.
Steaks were equilibrated to room temperature (68°F) prior to cooking and raw weight was collected. Steaks were cooked on an electric clam-shell grill (Cuisinart Electric Griddler GR5BP1, Cuisinart, Stamford, CT) preheated to 350°F to an internal temperature of 145°F. The internal temperature of the steaks was monitored with a thermocouple probe (Omega KHSS-18G-RSC-12, Omega Engineering, Inc., Norwalk, CT) placed in the center of each steak connected to a handheld thermometer (Omega HH801B, Omega Engineering, Inc., Norwalk, CT). Steaks were removed from the grill and allowed to cool for a minimum of 5 minutes. After the initial cooling period, cooked steaks were weighed and cooking loss percentage calculated. Warner-Bratzler shear force was conducted from a minimum of six cores (0.5 in. diameter) were removed from the center of each steak parallel with the muscle fibers. Each core was placed in the middle of a V-notched (60-degree-angle) cutting blade. All cores were perpendicularly sheared to the muscle fibers at the shear force machine (Tallgrass Solutions GF-151, Tallgrass Solutions, Inc., Manhattan, KS).