scholarly journals Combined Impacts of Two Type's Cold Storage and Microwave Radiation on Stored Products Insects and Wheat Seed Viability

2018 ◽  
Vol 5 (2) ◽  
pp. 121-129
Author(s):  
Nasim Bayramzadeh ◽  
Ali Pourmirza
2002 ◽  
Vol 57 (2-3) ◽  
pp. 7
Author(s):  
N. I. Grigor'eva ◽  
L. M. Chepel ◽  
S. P. Sirenko ◽  
T. M. Cheshko ◽  
V. I. Kiyko

Weed Science ◽  
2009 ◽  
Vol 57 (1) ◽  
pp. 124-132 ◽  
Author(s):  
Ryan L. Nielson ◽  
Marc A. McPherson ◽  
John T. O'Donovan ◽  
K. Neil Harker ◽  
Rong-Cai Yang ◽  
...  

Development of genetically modified (GM) wheat has raised concerns about the movement and persistence of transgenes in agroecosystems and the ability of growers to segregate GM from conventional wheat. Wheat as a crop has been studied extensively but the population biology of volunteer wheat is not well characterized. Artificial seed bank studies were conducted in western Canada to provide baseline data on volunteer wheat seed persistence. Seed from two cultivars of Canadian western red spring wheat, ‘AC Splendor’ and ‘AC Superb’, were buried in mesh bags at three depths (0, 2, and 15 cm) in two different environments in the fall of 2003 and 2004. In addition, in 2004, ‘AC Superb’ seed were separated into small and large seed lots and buried with a medium seed lot to examine the influence of seed size on seed bank persistence. Seeds were withdrawn at intervals to assess seed germination and viability and regression analysis conducted on the viable seed at each sample period, after burial. Seed viability was variable within years and sites, and declined exponentially over time. In the spring, approximately 6 mo after initiation, viable seed ranged from 1 to 43%. With the exception of a single site and year, seeds on the soil surface persisted significantly longer than buried seeds and increasing burial depth accelerated loss of viability. The maximum viability of wheat seeds at 0, 2, and 15 cm depth in the spring following planting was 43, 7, and 2%, respectively. The extinction of viability for 99% (EX99) of the seed was estimated from regression analysis. The EX99values of seeds buried at 0, 2, and 15 cm ranged from 493 to 1,114, 319 to 654, and 175 to 352 d after planting (DAP), respectively, with the exception of one site in 2003 where burial depths were not different and all had an EX99value of 456 DAP. Seed size and cultivar did not significantly affect persistence, with the exception of one site in 2003 where the difference in EX99values was 20 DAP. The rapid loss of seed viability limits temporal gene flow via volunteers in years following a wheat crop. Results provide data on spring wheat biology to aid in Canadian environmental biosafety assessments of GM wheat and will be incorporated into a mechanistic model to predict wheat gene flow on the Canadian prairies.


2013 ◽  
Vol 35 (3) ◽  
pp. 361-367 ◽  
Author(s):  
Tereza Cristina de Carvalho ◽  
Francisco Carlos Krzyzanowski ◽  
Osvaldo de Castro Ohlson ◽  
Maristela Panobianco

The assessment of the germination test in wheat seeds varies from 4 to 15 days, because the species normally presents dormancy in freshly harvested seeds. The tetrazolium test can characterize seed viability in less than 24 hours including lots with dormancy seeds. The objective of this study was to develop a practical and efficient procedure for evaluating the viability of wheat seeds using the tetrazolium test. Five seed lots of the BRS 208 cultivar were used, where the following were tested: a) pre-conditioning between moist paper towels or direct immersion in water for 18 hours, at 20 °C; b) longitudinal section of the embryo and the endosperm; c) coloration on paper or by immersion for 2 and 3 hours, at 30 and 40 °C; and d) concentrations of tetrazolium solution at 0.075%, 0.1%, 0.5% and 1.0%. The tetrazolium test may be efficiently used to evaluate wheat seed viability by pre-conditioning the seeds between paper towels (18 hours, at 20 °C) and adopting the following combinations of preparation and coloration: coloration of both halves of the seed on paper (2 hours, at 30 °C), in a 1.0% tetrazolium solution; or coloration of one half of the seed by immersion (3 hours, at 30 °C), in a 0.1% tetrazolium solution; or coloration of one half of the seed by immersion (2 hours, at 40 °C), in a 0.075% tetrazolium solution. This latter procedure is recommended for identifying and discarding lots with lower viability.


2008 ◽  
Vol 36 (3) ◽  
pp. 710-720 ◽  
Author(s):  
S.L. Clement ◽  
R.C. Martin ◽  
J.E. Dombrowski ◽  
L.R. Elberson ◽  
M. Kynaston ◽  
...  

Author(s):  
Byron B. Lamont ◽  
Rosemary J. Newton ◽  
Pablo Gomez-Barreiro ◽  
Tianhua He

Seed viability is routinely measured on seeds that fail to germinate at the end of an experiment. Together with the number of germinants, this is used to estimate viability of the seeds at start of the experiment (i.e., initial viability) and provides the comparative basis on which germination success is determined. We used this standard procedure on 40 Leucadendron species subjected to oscillating temperatures, heat and/or smoke pre-treatments to examine the extent to which they raised germination levels above that of the untreated controls. 16 species showed significantly different levels of estimated initial seed viability between treatments when they should have been unaffected. Loss of viability during the trial was an order of magnitude greater than annual loss during cold storage, which was usually negligible. Lowest levels of estimated initial viability occurred among the poorly germinating controls and confirmed that the heat and smoke treatments had little effect on viability. Species with soil-stored seeds were more vulnerable to this artefact than those with plant-stored seeds. We caution against the routine use of end-of-trial germination and viability of ungerminated seeds as an estimate of initial viability in determining germination success of various treatments. The preference is for estimates of initial viability to be undertaken on a separate sample of seeds in association with the trial.


Rodriguésia ◽  
2021 ◽  
Vol 72 ◽  
Author(s):  
Suzana Targanski Sajovic Pereira ◽  
Wagner Aparecido Vendrame ◽  
Kathia Fernandes Lopes Pivetta ◽  
José Carlos Sorgato ◽  
Ricardo Tadeu de Faria

Abstract The objective of this study was to evaluate the efficiency of cryoprotective solution (PVS2) combined with phloroglucinol for the cryopreservation of seeds of two orchid species, Encyclia cordigera and Epidendrum ciliare. Seeds of Encyclia cordigera had 91.03% initial viability and 91.99% germination. The treatment of the seeds with PVS2 at 0 °C with 1% phloroglucinol for 60 min returned 93.79% viability and 91.01% germination after recovery from LN, consequently resulting in faster development of protocorms. For Epidendrum ciliare, seed viability was 85.65% and germination was 85.90%. Seed exposure to the PVS2 at 0 °C with 1% phloroglucinol for 180 min showed viability of 39.23% and germination of 37.88%. Despite lower germination, 78.90% of the protocorms reached stage P3 of development, when evaluated 45 days after sowing, not significantly different from the control 1, and showed normal development. These results indicate that PVS2 cryoprotective solution is efficient when combined with phloroglucinol for the cryopreservation and successful recovery of seeds of Encyclia cordigera and Epidendrum ciliare. The present study also indicates that response to cryopreservation and success of recovery after cold storage is species-specific and requires adjustments in exposure time to PVS2 at 0 °C prior to immersion in LN.


1996 ◽  
Vol 89 (6) ◽  
pp. 1638-1648 ◽  
Author(s):  
Steven L. Halverson ◽  
Wendell E. Burkholder ◽  
Timothy S. Bigelow ◽  
Erik V. Nordheim ◽  
Mark E. Misenheimer

2016 ◽  
Vol 107 (1) ◽  
pp. 73
Author(s):  
Ahad MOTALLEBI

The effect of microwave's radiation on seed viability of three different oilseed crops, spores of <em>Aspergillus niger </em>and quality of extracted oil from treated seeds over various exposure times was evaluated. The seeds were exposed to 2450 MHz. at five different power levels of 0, 100, 200, 400, 600 and 800 W for two exposure times of three and five minutes. At a given time, a direct negative relationship between seed viability and microwave's radiation power level was detected. Substantial variation in the lethality of tested seeds to microwave's power levels was apparent in the fiducial limits of the estimated LD<sub>50 </sub>values in probit analysis approach. A similar trend of <em>A. niger</em> spores’ susceptibility to microwave radiation was detected. The microwaves' radiation and exposure time did not impact one another and a significant interaction was not detected. Short term fungal infection did not cause substantial quantitative and qualitative damage to the oilseeds. The oil quality was generally unaffected by microwave radiation and fungal infestation for tested oilseeds. Moreover, microwave radiation decreased seed germination percentage and vigor index. The microwave radiation could provide an effective and friendly environmental treatment technique for improving the dietary consumption of the oil in any seed disinfestation program.


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