Computer control of blancher for french fry color

1992 ◽  
Vol 69 (9) ◽  
pp. 525-536 ◽  
Author(s):  
P. M. Tomasula ◽  
M. F. Kozempel ◽  
M. J. Kurantz ◽  
J. C. Craig
2021 ◽  
Vol 6 (2) ◽  
pp. 345-355
Author(s):  
Sastry S. Jayanty ◽  
◽  
Esam Emragi ◽  
David G. Holm

The effect of three field heat reduction methods, including temperature lowering stepwise (TLS), temperature lowering gradually (TLG), and temperature lowering immediately (TLI), after harvesting on the quality of Russet Norkotah 3 and red skin numbered line CO 07102-1R potatoes were investigated. The tubers were analyzed at harvest (0 time), when they reached 3 °C, and after 6 months of storage at 3 °C for physiological weight loss, firmness, wound healing, total phenolics content, reducing sugars, and color of french fries. The results indicated that weight and firmness losses were lower under the TLS reduction method after 6 months of storage than TLG and TLI methods. The weight loss in TLS is 12%, TLG 14% and TLI 17% in CO 07102-1R whereas Russet Norkotah TLS is 4%, TLG 6%, and TLI 8% respectively. Wound healing was more effective using the TLS reduction method, especially in Russet Norkotah 3. French fry color was lighter at harvest (USDA grade 0), while there were no differences in the color of French fries prepared from tubers stored under the TLS and TLG methods (both had USDA grade 2). French fries were darker for tubers from the TLI method (USDA grade 4). The total phenolic content and reducing sugars were significantly increased in the TLI field heat reduction method. Keywords: Potato, Storage management, Wound healing, Weight loss, French fry


HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 443f-443
Author(s):  
George H. Clough

Potato (Solanum tuberosum) cv. `Russet Burbank' response to source of side-dress Ca fertilization applied at 0, 28 and 56 kg·ha-1 Ca on fine sandy loam soil was evaluated. Side-dress Ca source and rate did not affect number or total weight of tubers/hill, average tuber weight, or tuber macronutrient concentrations at mid-season. Tuber B concentration was significantly greater with the 12-0-0-10.5 source as compared to the check. Tuber Fe concentration decreased linearly as 22-0-0-7 rate increased from 0 to 56 kg·ha-1 Ca. No other micronutrient concentration was affected by the applied treatments. Calcium fertilization had no effect on tuber yield, grade distribution, or specific gravity. The predominant internal defect observed was brown center, which was reduced at harvest by side-dress Ca application. Internal quality and french fry color were evaluated after storage for 4 months.


1974 ◽  
Vol 51 (5) ◽  
pp. 170-173 ◽  
Author(s):  
W. M. Iritani ◽  
Larry Weller

HortScience ◽  
1997 ◽  
Vol 32 (4) ◽  
pp. 728-732 ◽  
Author(s):  
Stephen L. Love ◽  
Bruce K. Werner ◽  
Horia I. Groza ◽  
Asunta Thompson-Johns

Nine commercially available true potato seed (TPS) hybrids were compared to four standard clonal cultivars with respect to mean and uniformity of foliar characteristics and tuber traits important to the North American potato industry. The TPS hybrids were planted using second vegetative generation tubers derived originally from botanical seed. Ten plants from each plot were individually evaluated for plant height, vine maturity, early blight symptoms, and verticillium wilt symptoms. Following harvest, yield was determined and the tubers were rated or measured for appearance, shape, specific gravity, and french fry color. The TPS hybrids had mean values for all tuber and foliar traits, except plant height, that were not significantly different from those of one or more of the cultivars; generally, values for the hybrids fell amid those of the cultivars. Two of the hybrids were taller on average than any of the four cultivars. In contrast to the means, trait uniformity of the TPS hybrids was consistently less than for the cultivars. For all foliar traits, except plant height, the TPS hybrids were substantially less uniform than the standard cultivars. For specific gravity and french fry color, two important processing quality traits, the hybrids tended to be less uniform than the cultivars; however, the difference was much less pronounced than for the foliar traits. Four of the hybrids were not significantly less uniform than one or more of the cultivars for french fry color and seven were not less uniform for specific gravity. For many market uses, the TPS hybrids appeared to have the tuber yield and quality characteristics needed to compete with standard clonally propagated cultivars.


HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 645a-645
Author(s):  
Stephen L. Love ◽  
Asunta Thompson-Johns ◽  
Timothy P. Baker

Eight hundred and fifty-three clones of Russet Burbank and 1012 clones of Lemhi Russet were obtained from Native Plants, Inc. in 1988. The clones were produced via a tissue culture system designed to produce somoclonal variants. Four cycles of selection were completed from 1988-1991. Selection was based on resistance to blackspot bruise, a tuber flesh discoloration caused by condensation of free tyrosine; or the ability to produce light french fry color following cold storage. At the end of the four selection cycles all but six Russet Burbank clones and seven Lemhi Russet clones were eliminated. ANOVA across years was completed for the eleven somaclonal variants and Russet Burbank and Lemhi Russet checks. Of the Russet Burbank clones, three were significantly (p = .05) more resistant to blackspot bruise and one had significantly better fry color after cold storage. All four clones had significantly reduced yield in comparison to the check clones. Of the Lemhi Russet clones, three were significantly more resistant to blackspot bruise, and four had significantly better fry color than the check clone. Only one of the seven clones (one with superior fry color designated L1908) did not show a significantly lower yield potential.


Author(s):  
D.R. Ensor ◽  
C.G. Jensen ◽  
J.A. Fillery ◽  
R.J.K. Baker

Because periodicity is a major indicator of structural organisation numerous methods have been devised to demonstrate periodicity masked by background “noise” in the electron microscope image (e.g. photographic image reinforcement, Markham et al, 1964; optical diffraction techniques, Horne, 1977; McIntosh,1974). Computer correlation analysis of a densitometer tracing provides another means of minimising "noise". The correlation process uncovers periodic information by cancelling random elements. The technique is easily executed, the results are readily interpreted and the computer removes tedium, lends accuracy and assists in impartiality.A scanning densitometer was adapted to allow computer control of the scan and to give direct computer storage of the data. A photographic transparency of the image to be scanned is mounted on a stage coupled directly to an accurate screw thread driven by a stepping motor. The stage is moved so that the fixed beam of the densitometer (which is directed normal to the transparency) traces a straight line along the structure of interest in the image.


Author(s):  
Kenneth H. Downing

Three-dimensional structures of a number of samples have been determined by electron crystallography. The procedures used in this work include recording images of fairly large areas of a specimen at high tilt angles. There is then a large defocus ramp across the image, and parts of the image are far out of focus. In the regions where the defocus is large, the contrast transfer function (CTF) varies rapidly across the image, especially at high resolution. Not only is the CTF then difficult to determine with sufficient accuracy to correct properly, but the image contrast is reduced by envelope functions which tend toward a low value at high defocus.We have combined computer control of the electron microscope with spot-scan imaging in order to eliminate most of the defocus ramp and its effects in the images of tilted specimens. In recording the spot-scan image, the beam is scanned along rows that are parallel to the tilt axis, so that along each row of spots the focus is constant. Between scan rows, the objective lens current is changed to correct for the difference in specimen height from one scan to the next.


Author(s):  
R. J. Lee ◽  
J. S. Walker

Electron microscopy (EM), with the advent of computer control and image analysis techniques, is rapidly evolving from an interpretative science into a quantitative technique. Electron microscopy is potentially of value in two general aspects of environmental health: exposure and diagnosis.In diagnosis, electron microscopy is essentially an extension of optical microscopy. The goal is to characterize cellular changes induced by external agents. The external agent could be any foreign material, chemicals, or even stress. The use of electron microscopy as a diagnostic tool is well- developed, but computer-controlled electron microscopy (CCEM) has had only limited impact, mainly because it is fairly new and many institutions lack the resources to acquire the capability. In addition, major contributions to diagnosis will come from CCEM only when image analysis (IA) and processing algorithms are developed which allow the morphological and textural changes recognized by experienced medical practioners to be quantified. The application of IA techniques to compare cellular structure is still in a primitive state.


Author(s):  
L. S. Chumbley ◽  
M. Meyer ◽  
K. Fredrickson ◽  
F.C. Laabs

The Materials Science Department at Iowa State University has developed a laboratory designed to improve instruction in the use of the scanning electron microscope (SEM). The laboratory makes use of a computer network and a series of remote workstations in a classroom setting to provide students with increased hands-on access to the SEM. The laboratory has also been equipped such that distance learning via the internet can be achieved.A view of the laboratory is shown in Figure 1. The laboratory consists of a JEOL 6100 SEM, a Macintosh Quadra computer that acts as a server for the network and controls the energy dispersive spectrometer (EDS), four Macintosh computers that act as remote workstations, and a fifth Macintosh that acts as an internet server. A schematic layout of the classroom is shown in Figure 2. The workstations are connected directly to the SEM to allow joystick and computer control of the microscope. An ethernet connection between the Quadra and the workstations allows students seated there to operate the EDS. Control of the microscope and joystick is passed between the workstations by a switch-box assembly that resides at the microscope console. When the switch-box assembly is activated a direct serial line is established between the specified workstation and the microscope via the SEM’s RS-232.


Author(s):  
Kenneth S. Vecchio ◽  
John A. Hunt

In-situ experiments conducted within a transmission electron microscope provide the operator a unique opportunity to directly observe microstructural phenomena, such as phase transformations and dislocation-precipitate interactions, “as they happen”. However, in-situ experiments usually require a tremendous amount of experimental preparation beforehand, as well as, during the actual experiment. In most cases the researcher must operate and control several pieces of equipment simultaneously. For example, in in-situ deformation experiments, the researcher may have to not only operate the TEM, but also control the straining holder and possibly some recording system such as a video tape machine. When it comes to in-situ fatigue deformation, the experiments became even more complicated with having to control numerous loading cycles while following the slow crack growth. In this paper we will describe a new method for conducting in-situ fatigue experiments using a camputer-controlled tensile straining holder.The tensile straining holder used with computer-control system was manufactured by Philips for the Philips 300 series microscopes. It was necessary to modify the specimen stage area of this holder to work in the Philips 400 series microscopes because the distance between the optic axis and holder airlock is different than in the Philips 300 series microscopes. However, the program and interfacing can easily be modified to work with any goniometer type straining holder which uses a penrmanent magnet motor.


Sign in / Sign up

Export Citation Format

Share Document