The Seed Technologist Newsletter
A newsletter for
The Association of Official Seed Analysts & The Society of Commercial Seed Technologist
Volume 83, Number 2 May, 2009
Seed Technology Newsletter Volume 83, No. 2 1 May, 2009
2008 - 2009 AOSA EXECUTIVE BOARD INFORMATION
Brent Turnipseed, President SDSU Seed Lab Plant Science Dept. P.O. Box 2207A, Ag Hall 227 Brookings, SD 57007 PH: 605-688-4589 Email: [email protected] FAX: 605-688-4013
Michael Stahr, Vice-President Dan Curry, Secretary-Treasurer Iowa State University Director of Seed Services Oregon State University 128A Seed Science Center 107 Crop Science Building Ames, IA 50011 Corvallis, OR 97331 PH: 515-294-0117 PH: 541-737-5094 Email: [email protected] Email: [email protected] FAX: 515-294-8303 FAX: 541-737-1589
Board Members Aida Galarza Michael Gill Georgia Dept. of Ag. Atlanta Seed Laboratory New Mexico Dept. of Ag. State Seed Laboratory Rm. 536 Ag. Bldg., Capitol Square MSC 3190 19 M.L. King, Jr. Dr. SW P.O. Box 30005 Atlanta, GA 30334 Las Cruces, NM 88003-8005 PH: 404-656-3635 PH: 505-646-3407 Email: [email protected] Email: [email protected] FAX: 404-657-8378 FAX: 505-646-1841
Janine Maruschak Victor Shaul CFIA Saskatoon Lab Washington State Department of Agriculture Seed Seed Science and Tech. Section Program 301-421 Downey Rd. 21 N. 1 st Ave. #203 Saskatoon, Saskatchewan Yakima, WA 98902 Canada S7N 4L8 PH: 509-225-2630 PH: 306-975-5832 Email: [email protected] Email: [email protected] FAX: 509-454-4395 FAX: 306-975-6450
Pat Stowe Johnny Zook North Carolina Dept. of Agriculture and Consumer Services Pennsylvania Dept. of Ag. Seed Section NCDA and Consumer Services 2301 N. Cameron St. PO Box 27647, 216 West Jones Street Harrisburg, PA 17110-9408 Raleigh, NC, 27603 PH: 717-787-4894 PH: (919) 733-3930 Email: [email protected] Email: [email protected] FAX: 717-705-6518 FAX: (919) 733-1041
Anita Hall, AOSA Executive Assistant Association of Official Seed Analysts 101 East State St., #214 Ithaca, NY 14850 [email protected] PH: 607-256-3313
Seed Technology Newsletter Volume 83, No. 2 2 May, 2009
2008 - 2009 SCST EXECUTIVE BOARD
President Vice President Gil Waibel, RST Doug Miller, RGT Wyoming Seed Analysis Lab Illinois Crop Improvement Assn. 749 Road 9 3105 Research Rd. Powell, WY P.O. Box 9013 82435307-754-4750 Champagne, IL 61826 Fax 307-754-4932 217-359-4053 [email protected] Fax: 217-359-4075 [email protected]
Director-at-Large Director-at Large Director-at Large Sue Alvarez, Terry Dunfield Jane Penrose, RST RST Seminis Vegetable Seeds J & T Green Seed Services Agri Seed Testing 2700 Camino del Sol Division726 Shoshone Ave. W 1930 Davcor Ct. SE Oxnard, CA 93030 Ste. 9 Twin Falls, ID 83301208- Salem, OR 97302 805-918-2469 733-3506 503-585-1440 Fax: 805-918-2424 [email protected] FAX: 503-588-0733 [email protected] [email protected]
Director-at Large Director-at Large Michael Stahr, CGT Jean Tolliver, RST 128A Seed Science Center Monsanto Seed Tech. Ctr. Iowa State University 460E. Adams St. Ames, IA 50011 Waterman, IL 60556 515-294-0117 815-264-8142 Fax: 515-294-8303 Fax: 815-264-7940 [email protected] [email protected]
Executive Director Anita Hall 101 East State Street PMB #214 Ithaca, NY 14850 607-256-3313 Fax 607-256-3313 [email protected]
Seed Technology Newsletter Volume 83, No. 2 3 May, 2009
SEED TECHNOLOGIST NEWSLETTER EDITORIAL STAFF
AOSA EDITOR SCST EDITOR Cindy Finneseth Sue Alvarez, Seed Testing Coordinator RST Seminis Vegetable Seeds Division of Regulatory Services 2700 Camino del Sol University of Kentucky Oxnard, CA 93030 103 Regulatory Services Bldg. 805-918-2469 Lexington, KY 40546-0275 Fax: 805-918-2424 859-257-2785 [email protected] Fax 859-323-9931 [email protected]
NORTHWEST I MIDWEST IIA Maryanne Triggs Washington State Dept. Jim Lair of Ag. USDA/ NASS – Grain Yields Lab 21 N. 1st Ave., Suite 203 c/o IL. Department of Agriculture Yakima, WA 98902 801 Sangamon Ave., P.O. Box 19281 509-225-2630 Springfield, IL 62794 Fax 509-454-4395 217-492-4295 Ext. 254 [email protected] Fax 217-492-4291 [email protected]
MIDWEST IIB NORTHEAST III SOUTHWEST IV Ronny Parmely Norma Rossel Donna Grubisic SDSU Seed Lab Johnny’s Selected Seeds MD Seed Analysis, Inc. P.O. Box 2207-A 955 Benton Avenue PO Box 40335 Brookings, SD 57007 Winslow, ME 04901 Santa Barbara, CA 93140 605-688-6636 207-861-3939 ext. 301 805-962-0739 Fax 605-688-4013 Fax 207-861-8381 805-962-0927 [email protected] [email protected] [email protected]
SOUTHERN V CANADA BOOKSHELF Aaron Palmer Doug Ashton Harold Armstrong Arkansas State Plant Board CSAAC Monsanto #1 Natural Resources Dr. 108 Vaughan St 460 E. Adams St. Little Rock, AR 72205 Almonte, ON Waterman, IL 60556 501-225-1598 CANADA , K0A 1A0 815-264-8142 Fax 501-225-7213 613-256-7411 Fax: 815-264-7940 [email protected] Fax 613-256-0485 [email protected] [email protected]
Subscription: $35.00 per year, U.S. Funds. Includes; three newsletter publications and the conference proceedings. For subscriptions, contact Anita Hall, SCST Executive Director/AOSA Executive Assistant at [email protected], or 607-256-3313, or visit the AOSA website: www.aosaseed.com.
The Seed Technologist Newsletter is published jointly by the Society of Commercial Seed Technologists, Inc. and the Association of Official Seed Analysts, Inc.
Seed Technology Newsletter Volume 83, No. 2 4 May, 2009
TABLE OF CONTENTS 2008 - 2009 AOSA EXECUTIVE BOARD INFORMATION ...... 2 2008 - 2009 SCST EXECUTIVE BOARD ...... 3 SEED TECHNOLOGIST NEWSLETTER EDITORIAL STAFF ...... 4 TABLE OF CONTENTS ...... 5 NOTES FROM THE EDITORS ...... 6 EXECUTIVE BOARD REPORTS ...... 7 SCST PRESIDENTIAL REPORT ...... 7 AOSA PRESIDENTIAL REPORT ...... 8 AOSA/SCST 2009 ANNUAL MEETING ...... 9 2009 ANNUAL MEETING INFORMATION ...... 9 ANNUAL MEETING SCHEDULE ...... 10 2009 RESEARCH PAPER ABSTRACTS ...... 12 Comparison of Two Accelerated Aging Test Methods ...... 12 How to Produce and Assure Uniformity in Master Calibration Samples ...... 13 Comparison of Inert Matter Content Separated from Tall Fescue Samples Using the AOSA Manual Method and a Uniform Blowing Procedure ...... 14 POSTER ABSTRACTS ...... 15 A High –throughput System for Integrated Extraction and PCR Amplification of DNA from Seed and Leaf Tissue for Plant Genotyping Studies ...... 15 Laboratory methods to break dormancy in eastern gamagrass (Tripsacum dactyloides L.) seeds .. 16 Svalbard Global Seed Vault: Safeguarding the Future of Agriculture ...... 16 Preservation of Plant Genetic Resources at the National Center of Genetic Resources Preservation ...... 17 The NCRPIS - Providing Diverse Plant Genetic Resources for Worldwide Research and Development...... 18 Annonaceae seeds: Desiccation tolerant with unusual physiologies ...... 18 The Effect of Seed Vigor on the Uniformity of Soybean Seedling Emergence ...... 19 Identification of Foxtail (Setaria) Impurities: Examination and Comparison of Four Species ...... 20 National Seed Herbarium of Canada ...... 21 Differential Scanning Calorimetry as a Tool for Nondestructive Measurements of Seed Deterioration in Lettuce (Lactuca sativa, CV “Black Seeded Simpson”) ...... 21 Cryogenic Storage of Cereal Grains: Results from a 20 Year Experiment ...... 22 Seed Storage Containers: Implications of water permeability properties on moisture management 23 Identification and Characteristics of Solanum, Physalis, Datura, and Quincula species ...... 23 Bonafide BDI® – Rye grass, A Novel, DNA based Diagnostic tool for Adventitious Presence test in Perennial Ryegrass ...... 24 SEED ISSUES FORUM ...... 24 WORKSHOPS AT THE ANNUAL MEETING ...... 25 Agenda for the Endophyte Testing Workshop ...... 25 Statistics Workshop June 1, 2009 Colorado State University ...... 26 PATHOLOGY/GENETIC TECHNOLOGY WORKSHOP ...... 27 Seed Technology Workshop ...... 27 COMMITTEE REPORTS ...... 28 CONSOLIDATION TASK FORCE REPORT ...... 28 Recommended Consolidation Plan ...... 29 Recommended Consolidation Plan for Elected Officers ...... 30 Appendix A. Consolidation Time Line ...... 31
Seed Technology Newsletter Volume 83, No. 2 5 May, 2009
History of Consolidation Effort ...... 32 RESEARCH IS THE WAY TO INNOVATE AND IMPROVE SEED TESTING ...... 34 GENERAL AND TECHNICAL INFORMATION ...... 36 MASTER CALIBRATION USAGE DATA ...... 36 ENCRUSTED COOL SEASON GRASS REFEREE ...... 39 BOOKSHELF ...... 49 ANNOUNCEMENTS ...... 50 NORTHEAST SEED ANALYST WORKSHOP ANNOUNCEMENT ...... 50 IDAHO SEED ANALYSTS ASSOCIATION WORKSHOP REVIEW ...... 51 SPOTLIGHT ON AN ANALYST ...... 52 PRINCIPLES OF SEED TESTING DVDS ...... 57 PRINCIPLES OF SEED TESTING DVDS ORDER FORM ...... 58 SEED PRODUCTION DVDS ...... 59 SEED PRODUCTION DVDS ORDER FORM ...... 60 TRAINING OPPORTUNITIES AT THE ISU SEED SCIENCE CENTER ...... 61 UPCOMING FEDERAL SEED SCHOOLS IN GASTONIA, NC ...... 61 EMPLOYMENT OPPORTUNITIES ...... 62 JOB ANNOUNCEMENT- QUALITY MANAGER JOHNNY’S SELECTED SEEDS ...... 62 HORTICULTURAL INSPECTOR 3 (BIOTECHNOLOGY), DIVISION OF PLANT INDUSTRY ...... 64 CALENDAR ...... 65
NOTES FROM THE EDITORS
The Newsletter Committee is always looking for additional members. Please join us for our Committee Meeting on Tuesday, June 2 at 8:00 am. We will divvy up responsibilities for the annual meeting and the upcoming year and plan to discuss some exciting projects and a potential face-lift for the Newsletter.
Please consider submitting an article to the newsletter. Articles can be submitted at any time. Don’t wait for the deadline! Anyone can submit an article, but we consider the appropriateness and timing, and will not break copyright laws. We reserve the right to edit, but will not change content.
Some suggestions for articles: Seed testing or method ideas, Analyst news, Lab spotlight, General interest, Technical information, Workshop announcements, Seed school announcements and Meeting summaries or announcements.
Cindy Finneseth, AOSA Editor and Sue Alvarez, SCST Editor Deadline for the September 2009 Newsletter Issue: August 15, 2009
Submit articles by email to Cindy Finneseth, Sue Alvarez or your regional editor. Find the names and contact information on page 4. Websites AOSA (www.aosaseed.com) SCST (www.seedtechnology.net)
Seed Technology Newsletter Volume 83, No. 2 6 May, 2009
EXECUTIVE BOARD REPORTS
SCST Presidential Report
The annual meeting is just around the corner and I hope many of you will be able to attend. The consolidation of SCST and AOSA will be up for consideration. The proposed by-laws and a recommended consolidation plan are included in this newsletter. Additional information is available on the Consolidation Task force webpage: http://www.seedtechnology.net/Consolidation.htm. The Consolidation Task force must be thanked for their massive three year effort in putting this proposal together for us. For the most part, the current by-laws of SCST and AOSA serve as the basis of the proposed by-laws. This is just a starting point, since by-laws are open for change every year. In fact, our current by-laws are far from perfect. This year shows more than ever the need to consolidate. Traveling freezes and finances will affect our attendance at the Fort Collins meetings. We have so much to do in our organizations, and not enough resources to accomplish our charter. Please carefully consider the consolidation information and come to the meeting prepared to discuss this important issue. If you are unable to attend the meeting send the Executive Board or Consolidation Task Force your comments.
At the conclusion of the 2009 meeting, my term as President will end. I want to thank the SCST members for the opportunity to serve on the Executive Board and as its President. I wholly recommend such involvement. My view of the seed industry and how it works has broadened in ways I could not imagine. I have also met many people in our sister seed industry organizations, both nationally and internationally. It has also been a wonderful opportunity to meet and work with many SCST members I did not know before. Anyway – thank you!
In the last few months I have represented SCST at the ASTA Flower and Vegetable meeting, and the AOSCA winter meeting. The take-away message for SCST at these meetings is the real need for accurate and uniform seed testing results. There are many reasons why results can vary, and they are not all in our control. Sampling is always a big issue, while this is usually outside our control we can help educate our seed industry about proper sampling techniques. There are some areas we do directly control. When variability in testing results occurs, it costs the seed industry by inaccurately managing and pricing a seed lot, potential stop sales, and reputation. Buyers of seed rely on the accuracy of the information on the seed label. We must keep striving for highly accurate and uniform results. The resources we have to accomplish accurate and uniform results are through the training and education of analysts, and the use and proper interpretation of the rules. I recommend we all examine how we are testing seeds, and introspectively ask if we are properly testing by the AOSA Rules in all of our testing efforts. We must keep working on adding to, and improving the rules. Striving for accuracy and uniformity in testing is our biggest challenge as professionals and as an organization.
Seed Technology Newsletter Volume 83, No. 2 7 May, 2009
I look forward to seeing everyone who is able to come to the meetings this year. If you would like to be more involved, please look for opportunities to help this year. There is plenty of work to keep us all busy.
Sincerely, Gil Waibel, RST
AOSA Presidential Report
It is hard to believe that the annual meeting is just a few short weeks away. The host committee has put together an excellent program and our committees are hard at work preparing for their meetings. The Consolidation Task Force has put a tremendous amount of work into a draft Constitution and Bylaws for the consolidated organization, and a recommended Consolidation Plan. Both of these important documents are included in this newsletter and available on the AOSA website. Please take the time to carefully review these documents and bring your comments and concerns to the meeting. As you consider the possible merging of the AOSA and SCST, keep in mind what is best for AOSA long term, not just what you’d like for your lab or yourself! Keep an open mind to carefully weigh the benefits versus the cons of a potential merger. If you are unable to attend the meeting please contact me, one of your board members or Loren Weisner, the Consolidation Task Force Chair.
Many laboratories are facing tough times during this economic recession. Most of us will be expected to do more with less. This is true of both AOSA and SCST laboratories. While we all have to cope with economic limitations we also have to remember the important role seed testing and our organization plays in the seed industry. We still need to make the effort to participate in referee projects and committee activities, attend local industry meetings, and generally remain involved in our industry despite increased financial pressure. Please don’t hesitate to contact AOSA if you need support or assistance in explaining why your program is fundamental to the success of American agriculture.
I have enjoyed serving AOSA as president for the last two and half years. The experience has been extremely interesting and educational. I have had the opportunity to work with members of the seed industry from the US and all over the world. Making friends and contacts across the nation and world are vital to our organization. I now have a better understanding of the important role our organization plays both nationally and internationally. I hope many of you will consider serving AOSA as an officer or board member. While it is a responsibility to serve the AOSA, I guarantee you will get more out of the experience than you will put into it.
I hope to see you all in Fort Collins. Sincerely, Brent Turnipseed, AOSA President
Seed Technology Newsletter Volume 83, No. 2 8 May, 2009
AOSA/SCST 2009 ANNUAL MEETING
2009 Annual Meeting Information
The 2009 AOSA-SCST Annual Meeting is being hosted by the Front Range Seed Analysts in Fort Collins, CO, May 31 - June 5, 2009. The meeting is an excellent opportunity for you to appreciate all the activities AOSA and SCST are involved in. The meeting schedule is filled with committee meetings, Referee Projects, Research Papers Symposium, the Seed Issues Forum, Seed Technology Workshop, Open Rules Committee Meeting, Long Range Planning and Business Meetings. The meeting will also offer many opportunities to interact and network with your fellow seed analysts. There will also be a post convention bus tour to the stunningly beautiful Rocky Mountain National Park.
Please review the updated meeting information included in this newsletter and check the website for current information.
Visit the AOSA and SCST websites for complete on-line registration, on-line hotel reservations, workshop agendas, transportation and local information. The hotel phone number is 1-970-482-2626 if you wish to contact them directly. We hope to see you in beautiful Colorado!
http://www.seedtechnology.net/2009/2009_AOSA-SCST.htm http://www.aosaseed.com/2009/2009_AOSA-SCST.htm
Seed Technology Newsletter Volume 83, No. 2 9 May, 2009
Annual Meeting Schedule Time/Date Meeting/Event Saturday 5/30/2009 6:00 - 6:30pm Meeting with RGT Exam Candidates Sunday 5/31/2009 7:00am - 5:00pm Registration 7:00am - 5:00pm Business Office 7:45am - 6:00pm Endophyte Workshop 8:00am - 5:00pm SCST Board Meeting 8:00am - 2:00pm RGT Exam 8:00am - 5:00pm RGT Exam Grading 6:00pm - 7:00pm RGT Exam Results 7:00pm - 8:00pm Meeting with RST Exam Candidates
Monday 6/1/2009 7:00am - 5:00pm Registration 7:00am - 5:00pm Business Office 8:00am - 5:00pm Statistics Workshop (CSU) 7:30am - 5:00pm Pathology/Biotech Workshop (STA) 8:00am - 2:00pm RST Examination (CSU) 8:00am - 5:00pm RST Grading (CSU) 8:00am - 4:00pm AOSA Board Meeting 4:00pm-6:00pm AOSA-SCST Joint Board Meeting 10:00am - 10:30am Morning Break 12:00pm - 1:00pm Lunch for RST Exam and Statistics workshop 2:30pm - 3:00pm Afternoon Break 7:00pm - 8:00pm RST Exam results 8:00pm - 9:00pm Joint Committee Chair/Research Subcommittee Meeting
Tuesday 6/2/2009 7:00am - 5:00pm Registration 7:00am - 5:00pm Business Office 7:00am Bean Buddy Walk Run 8:00am - 9:00am Newsletter Committee 8:00am - 9:00am Digital Imagery Committee (formerly Computer) 8:00am - 9:00am AOSA By-laws Committee 9:00am - 10:00am Proficiency Testing Committee 9:00am - 10:00am Purity Committee 9:0am - 10:00am Referee Committee 10:00am - 12:00pm Opening Session and Brunch 10:00am - 12:00pm Exhibitor Set-up 12:00pm - 5:00pm Exhibits 12:30pm - 2:30pm Affiliates/Liaison Meeting 12:30pm - 2:30pm Rules Committee (closed) 12:15pm - 1:15pm Consolidation Discussion
Seed Technology Newsletter Volume 83, No. 2 10 May, 2009
1:15pm-2:15pm Research Papers 2:15pm - 2:30pm Afternoon Break 2:30pm - 4:00pm Referee Presentation/Buzz Session 5:00pm - 9:00pm Dinner- Terry Bison Ranch
Wednesday 6/3/2009 7:00am - 8:00pm Business Office/Registration 7:00am - 8:00am Breakfast 8:00am - 5:00pm Exhibits 8:00am - 10:00am Genetic Technology Committee 8:00am - 9:00am Conservation and Reclamation Seed Committee 8:00am - 9:00am Seed Technology Journal Committee 9:00am - 10:00am SCST Ethics Committee 9:00am - 10:00am Cultivar Purity/GMO Committee 9:00am - 10:00am Moisture Testing Committee 10:00am - 10:30am Morning Break 10:15am - 11:15pm Germination and Dormancy Committee 10:15am - 12:15pm Examination Committee (closed) 11:15am - 12:15pm Statistics Committee 11:15am - 12:15pm International Committee 12:00pm - 1:00pm Lunch- New AOSA & SCST Member Recognition 1:00pm - 2:00pm Imunnoassay Working Group 1:00pm - 2:00pm Tree and Shrub Committee 1:00pm - 3:00pm Rules Issues and Review Committee 2:00pm - 3:00pm Herbicide Bioassay Working Group 2:00pm - 4:00pm Vigor Committee 3:00pm - 4:00pm Teaching and Training Committee 4:00pm - 4:30pm Afternoon Break 4:00pm - 5:30pm Seed Technology Journal Workshop (open to all) 5:30pm - 6:00pm Seed Drop 6:00pm - 8:00pm Poster Session/Seed Issues Forum Reception
Thursday 6/4/2009 7:00am - 8:00pm Business Office/Registration 8:00am - 5:00pm Exhibits 7:00am - 8:00am Breakfast 8:00am - 9:00am Flower Seedling Committee 8:00am - 9:00am PCR Working Group 8:00am - 9:00am Seed Pathology Committee 9:00am - 12:00am Long Range Planning Session 10:00am Morning Break 12:00pm - 1:00pm Lunch- Anna Lute Award Presentation 1:00pm - 2:00pm Tetrazolium Committee 1:00pm - 2:00pm Electrophoresis Working Group
Seed Technology Newsletter Volume 83, No. 2 11 May, 2009
1:00pm - 2:00pm Handbook Committee 2:00pm - 2:15pm Afternoon Break 2:15pm - 5:15pm Open Rules Committee 6:00pm - 7:00pm Social Hour & Silent Auction 7:00pm - 10:00pm Banquet
Friday 6/5/2009 7:00am - 8:00pm Business Office/Registration 8:00am - 10:00am Exhibitors break down 7:00am - 8:00am Breakfast 8:00am - 10:00am Joint AOSA-SCST Rules Voting & Business Meeting 10:00am Morning Break 10:15am - 12:15pm SCST Business Meeting 12:15pm - 1:15pm Lunch 1:15pm - 3:15pm AOSA Business Meeting
Saturday 6/6/2009 all day Rocky Mountain National Park Bus Tour
2009 Research Paper Abstracts
Comparison of Two Accelerated Aging Test Methods 1S.G. Elias, 2R. Baalbaki, 3M.B. McDonald and J.M. Filho Oregon State University Seed Laboratory, California Dept. of Food and Agriculture, and Dept. of Horticulture and Crop Science at Ohio State University
Abstract The accelerated aging test (AAT) has been successfully used to evaluate seed vigor in a wide range of crop species for decades. Extensive studies with soybean (Glycine max [L.] Merrill) have standardized the laboratory variables that influence AAT. However, no published data are available to compare whether aging the seeds by placing them as one layer on the AA screen without weighing versus weighing the seeds before placing them on the screen would affect final germination results of the test. The objective of this study was to evaluate the effect of each method, i.e., aging the seeds as one layer vs. weighing seeds before the aging process has on final germination results. High (approximately 95% standard germination) and borderline quality (using the seed industry standard of approximately 85% standard germination) seed lots of soybean, sorghum (Sorghum bicolor L.) and tomato (Lycopersicon esculentum L.) were included in the study. Twelve commercial and public laboratories conducted the AAT in 2009 using both the one layer and weight methods for soybean, and six laboratories for each of the sorghum and tomato seed lots. The parameters, i.e., temperature, duration of aging, initial moisture content and
Seed Technology Newsletter Volume 83, No. 2 12 May, 2009
seed weight listed in the AOSA Seed Vigor Testing Handbook, 1983, were followed for both methods. The only exception was placing a single layer from the crop to be tested on the surface of the AA screen in one test and weighing the seed sample to be placed in each AA box as specified in Table 2 of the AOSA Seed Vigor Testing Handbook in the other. The International Seed Testing Association tolerance Table 15.5 was employed to determine whether the AAT germination results of the two methods were within tolerance in each laboratory. No significant differences in final AAT germination results were detected whether laboratories placed the seeds without weight in one layer on the AA screen or weighed the seeds as directed in the AOSA Seed Vigor Testing Handbook for all seed lots and crops used in the study. The only exception was in one laboratory for one soybean high quality sample where the variation between the two methods was significant. Variation among laboratories using the same method was found to be greater than variation between methods within the same laboratory. Based on these findings, either aging the seeds by placing them in one layer on the AA screen or weighing the seeds can be used without significant difference in final AAT germination results. These findings provide flexibility to laboratories in using either method depending on each laboratory’s preferences and circumstances.
How to Produce and Assure Uniformity in Master Calibration Samples Adriel Garay, Sabry Elias and Heather Nott Oregon State University Seed Laboratory
Abstract Calibration samples are used to calibrate seed blowers that are used to separate light inert matter in purity tests. It makes possible to find comparable optimum blowing points across blowers regardless of their physical variation. This contributes to uniform blowing procedure (UBP) across blowers and laboratories. As more grasses are entering national and international markets, such procedures will be needed. However, there is no established procedure how to develop uniform calibration samples and how to ensure their uniformity is maintained during their life span. The objective of this study was to develop a stepwise procedure to prepare uniform master calibration samples, using tall fescue as a model. The overall procedure requires several critical steps, including: finding the optimum blowing point for the species of interest; validating that point across samples; preparing calibration samples that can find that point; and verifying that all calibration samples are comparable to each other (uniform). The optimum blowing point was identified in tall fescue and was validated across samples representing different varieties, years and growing conditions. The validation studies used visual examination of florets according to the one-third caryopsis rule and by germinating the light and heavy fractions of samples. Preparation of Master Calibration Samples followed making sure the overlap of pure seed (colored red) and the light portion (colored green) would coincide with the desired optimum blowing point. The master calibration samples developed in this study found the blowing point accurately, consistently and efficiently. Finally, a set of calibration samples that are proven to be
Seed Technology Newsletter Volume 83, No. 2 13 May, 2009
uniform can be called “Master Calibration Samples”. The importance of maintaining uniformity throughout the life of the calibration samples as well as the potential applications and implications of this method for other temperate and tropical grass species is discussed.
Comparison of Inert Matter Content Separated from Tall Fescue Samples Using the AOSA Manual Method and a Uniform Blowing Procedure Adriel Garay, Sabry Elias and Heather Nott Oregon State University Seed Laboratory
Abstract The current method for separation of light inert matter in tall fescue ’TF’ (Festuca arundinaceae L.) is lengthy and depends primarily on individual’s visual interpretation to the one-third caryopsis development in the AOSA Rules. The Uniform blowing procedure (UBP) has been successfully used in inert matter assessment of Kentucky bluegrass and orchardgrass for decades. Similar UBP has been developed for tall fescue. The objective of this research was to determine whether the UBP for tall fescue would produce comparable results (within tolerance) to the current AOSA visual/manual method.
Two studies including commercial and certified samples with different varieties and inert matter levels from various years, 2003 (a drought year), 2004 and 2005 (normal years) were conducted to separate inert matter using both the UBP and the current AOSA method. The results showed that regardless of the variety, year, environment or the inert matter content, both methods produced comparable results, i.e., within tolerance in every case.
A national referee was conducted in 2007 to study the correlation between the current AOSA method and the UBP in assessing the inert matter of TF samples and compare the time saving between the two methods. The results showed that all participating laboratories separated comparable amount of inert matter i.e., within tolerance according to the AOSA Tolerance Table 13A, using both the UBP and the current AOSA method.
In 2008 a Northwest referee was conducted on eight TF samples that contained up to an average of 12% inert matter, and were considered problematic. The hypothesis was that the current AOSA method and the proposed UBP would give different results. Four laboratories from Oregon submitted the samples as they came from customers. Six Labs from Oregon, Washington, Idaho, and California participated in the referee. The results indicated that the inert matter separated by both the current AOSA method and the UBP were within tolerance for all samples by all laboratories with the exception of one sample with high multiple florets, which was within tolerance in three laboratories. Results indicated that variation among laboratories within the same method was greater
Seed Technology Newsletter Volume 83, No. 2 14 May, 2009
than the variation between the two methods.
The results of all the studies showed that both methods produce comparable results; hence the UBP can be used as an alternative to the current visual/manual method. Because of its mechanical nature, the UBP will contribute to simplicity, efficiency, standardization and consistency of test results within and among laboratories.
Poster Abstracts
This year we will have many interesting and educational posters on display during the Poster session and Seed Issue Forum. Make sure you plan to attend this dynamic and informative session!
A High –throughput System for Integrated Extraction and PCR Amplification of DNA from Seed and Leaf Tissue for Plant Genotyping Studies Steve Michalik Genomics Sigma-Aldrich, St. Louis, MO.
Abstract The Extract-N-Amp™ Plant and Seed PCR Kits contain all the reagents necessary to rapidly extract genomic DNA from plant leaves or seeds, respectively, and amplify targets of interest by PCR (Fig. 1). A novel Extraction Solution eliminates the need for conventional organic extraction of plant tissues, column purification, or precipitation of DNA. While mechanical disruption of seeds is necessary for successful extraction of DNA from seeds, we have found that our technology obviates the need for such processing of plant leaves. Not only do the kits provide all materials needed to effectively extract DNA, but they also include a PCR mix especially formulated for amplification directly from the extract. These PCR ReadyMix formulations contain dNTPs, buffer, MgCl2, and use an antibody-based hot start for specific amplification. The PCR master mixes come in two formulations: Extract-N-Amp™ PCR Reaction Mix and REDExtract-N-Amp™ Plant PCR Kit. The REDExtract-N-Amp™ PCR mix contains a dye that acts as a tracking dye and allows for convenient direct loading of PCR reactions onto agarose gels for analysis. Genomic DNA is extracted from 0.5 to 0.7 cm plant leaf disks that have been cut with a standard paper punch or from ground seed material. The leaf disk or ground seed is simply incubated in Extraction Solution for 10 minutes and then an equal volume of Dilution Solution or Neutralization Solution is added to the extract to neutralize inhibitory substances prior to PCR. A portion of the DNA extract is then added to a PCR reaction containing primers and either the REDExtract-N-Amp™ or Extract-N-Amp™ PCR.
Seed Technology Newsletter Volume 83, No. 2 15 May, 2009
Laboratory methods to break dormancy in eastern gamagrass (Tripsacum dactyloides L.) seeds Cindy L.H. Finneseth1* and Robert L. Geneve2 1Division of Regulatory Services, 103 Regulatory Services Bldg., University of Kentucky, Lexington, KY, 40546 USA. Email: [email protected]. 2Dept. of Horticulture, N-318 Ag. Science N., University of Kentucky, Lexington, KY 40546 USA. Email: [email protected].
Abstract Eastern gamagrass (Tripsacum dactyloides L.) is a widely-distributed native warm- season perennial grass with considerable utility including erosion control, wildlife planting, ornamental, forage, and as a biofuel source. Many cultivars, selections and ecotypes are available commercially. Plantings are most commonly established from seed; however, dormancy is a barrier to stand establishment. Development of one or more practical treatments to reduce dormancy and improve germination is of immediate commercial value to producers. The objective of this project was a practical assessment of laboratory methods for overcoming dormancy in eastern gamagrass. A single ‘Pete’ seed lot harvested in 2005 with an initial estimated viability of 74% based on tetrazolium (TZ) analysis was used for the experiments. Primary dormancy breaking treatments included: a) moist chilling, b) cupule removal, c) afterripening, d) predry, e) leaching, f) fire, g) charred wood extract, h) H2O2, i) GA3, j) KNO3, and k) scarification (chemical and physical). Seeds were exposed to treatments then germinated for 4 wks at 20/30°C. Fire and predry treatments were lethal; all other treatments except afterripening, leaching (48 hr), and GA3 (100 ppm), improved germination compared to the control (15%). Only moist chilling (6 wks at 10°C) was statistically superior at 52% germination, but 24% of the seed remained dormant after 4 wks at 20/30°C. An 18-hr soak in 15% H2O2 solution improved germination, but the effect was not consistent across experiments. Although not commercially feasible, the treatment combination of cupule removal and caryopsis scarification hastened germination and completely eliminated dormancy. At this time, moist chilling remains the most simple, effective and consistent dormancy-breaking treatment for eastern gamagrass, yet other dormancy- breaking chemicals and combinations of treatments may produce superior germination results. Additional research is necessary utilizing seed lots from other cultivars and harvest years.
Svalbard Global Seed Vault: Safeguarding the Future of Agriculture David Ellis The Plant Genetic Resources Preservation Program National Center for Genetic Resources Preservation, Fort Collins, CO
Abstract The National Center for Genetic Resources Preservation in Fort Collins Colorado coordinates the participation of the USDA-ARS National Plant Germplasm System (NPGS), along with 26 other genebanks from around the world, in a global effort to safeguard seeds of plants of importance to agriculture throughout the world by placing
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them in the Svalbard Global Seed Vault. Situated mid-way between the northern tip of Norway and the North Pole in a remote arctic island archipelago, the Svalbard Global Seed Vault marks its second year of operation in 2009. The Seed Vault currently contains over 400,000 seed collections from 220 countries, 31,000 of these samples from the NPGS. The vault entrance is ~430 feet above sea level, well above any predicted rise in sea level due to global warming. The vault consists of a 370 foot tunnel drilled into the solid rock permafrost in the side of a mountain leading to three seed storage rooms (~90’x30’x20’). The storage rooms and surrounding rocks are cooled to -18oC, although the permafrost will ensure the seed remains frozen in the unlikely event of a long-term power outage. The vault has no full time personnel on site, but local authorities have been enlisted to assist with security and any mechanical problems. The yearly operating expenses (estimated to be ~$200,000) are supported by the Global Crop Diversity Trust and the Government of Norway. The Seed Vault is managed by the Nordic Genetic Resource Center (NordGen) and continually monitored. Seed in the vault is stored free of charge under a deposit agreement. Ownership of the seed is retained by the donor and access is limited to the donor only. More information can be obtained at http://www.nordgen.org/sgsv.
Preservation of Plant Genetic Resources at the National Center of Genetic Resources Preservation David Ellis, The Plant Genetic Resources Preservation Program National Center for Genetic Resources Preservation, Fort Collins, CO
Abstract The National Center for Genetic Resources Preservation (NCGRP) in Fort Collins Colorado, with storage of over 750,000 collections of seed and vegetative propagules, safeguards one of the largest ex-situ collections of plant genetic resources in the world. This largest part of the collection is the base collection for the National Plant Germplasm System (NPGS) consisting of over 500,000 collections from 1,162 genera and 6,800 species (as of April 1, 2009). Almost 99% of these collections are stored as seed, usually consisting of 1000-3000 seed/collection. Seed collections are equilibrated (dried) to 6-10% moisture content and stored long-term (decades to centuries) at -18oC or in the vapor phase of liquid nitrogen (-175oC). Viability of the stored seed is initially assessed post-equilibration and then periodically as resources allow. All information on the collections is entered into the NPGS central database, the Germplasm Resources Information System (GRIN). Small research quantities of seed (25 – 100 seed) from all collections in the NPGS are distributed freely to qualified researchers throughout the world. In addition to the base collection at the NCGRP, the Center also provides duplicate back-up storage for important national and global collections. Examples of the duplicate storage include the global rice collection from the Philippines, the global wheat and maize collections from Mexico as well as collections from NGOs in the U.S.
Seed Technology Newsletter Volume 83, No. 2 17 May, 2009
The NCRPIS - Providing Diverse Plant Genetic Resources for Worldwide Research and Development. Maria Erickson1, 3, Lisa Pfiffner1, 3, Lisa Burke1, David Kovach1, Mark P. Widrlechner1, 2, Candice Gardner1, 2. 1 USDA-ARS Plant Introduction Research Unit, Ames, IA, 2 Adjunct Asst. Professor, Agronomy Dept., Iowa State University, Ames, IA, 3 Presenters
Abstract The North Central Regional Plant Introduction Station (NCRPIS) is an active plant genebank of the U.S. National Plant Germplasm System (NPGS). Dedicated to conserving and providing plant genetic resources and valuable information to researchers worldwide, the NPGS is a network of federal and state institutions and research units coordinated by the U.S. Department of Agriculture – Agricultural Research Service (USDA-ARS). The NCRPIS was established as the first Plant Introduction Station in 1948 in Ames, Iowa in cooperation with Iowa State University. Today, the NCRPIS collections contain over 1,400 different plant species and ca. 50,000 accessions of crop cultivars, elite lines, landraces, populations, and wild and weedy crop relatives (valuable sources of genetic diversity). Our poster will present an overview of these collections and the personnel who curate and conserve them. Our mission includes acquisition and conservation of genetically diverse crop germplasm and associated information, characterization, evaluation, distribution, enhancement and education. Plant germplasm is collected, regenerated, stored under controlled conditions, monitored for viability, and distributed to researchers and educators worldwide. Accessions with ample seed quantities are backed up at the National Center for Genetic Resources Preservation (NCGRP) in Ft. Collins, CO. Where applicable, NCRPIS collection viability is monitored according to AOSA seed testing rules in our AOSA-certified laboratory under the supervision of an AOSA-certified CSA. The lack of standardized viability-testing protocols for many species necessitates a prioritized, collaborative approach to germination research. We conduct research that supports conservation activities, crop improvement and germplasm utilization to meet a wide array of objectives. The expertise of our NCGRP research partners is important to achieving these objectives.
Annonaceae seeds: Desiccation tolerant with unusual physiologies Gayle M. Volk*, Remi Bonnart, and Christina Walters USDA-ARS National Center for Genetic Resources Preservation 1111 S. Mason St., Ft. Collins, CO 80521
Paw paw (Asimina triloba) is the only temperate species of the Annonaceae family. Wild paw paw trees can be found along the river valleys of the eastern and central United States and produce the largest fruits of any species native to North America. Paw paw seeds are reported to be classified as recalcitrant, with small embryos buried within a reticulate endosperm and a hard seed coat. We performed desiccation and low-temperature exposure experiments to determine if paw paw seeds have the potential for storage in ex situ genebanks. Germination was determined for seeds
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desiccated to between 3 and 35% moisture content (fresh weight basis) after either 7 or 15 weeks of stratification at 4oC. Seeds with 3% moisture content were also cooled to - 18oC. Our research revealed that paw paw seeds had high germination levels after - 18oC exposure for 24 h when stratified either before or after the desiccation treatment. Desiccation tolerance was also investigated for several tropical members of the Annonaceae family. Annona reticulata, Annona glabra, and Annona muricata seeds successfully germinated after desiccation, -18oC exposure, and gibberellic acid treatments. Additional seed storage experiments will determine how long Annonaceae seeds can be successfully stored within genebanks.
The Effect of Seed Vigor on the Uniformity of Soybean Seedling Emergence D.B. Egli and M. Rucker Department of Plant and Soil Sciences, University of Kentucky Lexington, KY 40546-0312
Abstract By definition, high vigor seed is expected to exhibit “… rapid, uniform emergence… in a wide range of field conditions”. The practical benefits of high-vigor seed in stress environments are well documented and they include higher levels of emergence that are reached sooner in comparison to low-vigor seed. Less is known about the effects of seed vigor on the uniformity of soybean (Glycine max L. Merr.) seedling emergence; consequently, our objective was to evaluate the effect of seed vigor on the timing of seedling emergence. Soybean seeds from seed lots with high standard germination (86 to 99%) and a range in accelerated-aging germination (42 to 94%) were planted 3.8 cm (1.5 inches) deep in soil-filled cups (3 seeds per cup and 100 seeds in each of two replications) in a greenhouse. Emergence (cotyledons above the soil surface) counts were taken at 6-hour intervals until emergence ceased. A four-term Gompertz model was used to describe emergence with time and to calculate a Uniformity Index (UI) - the hours from 10 to 90% of final emergence. Lowering soil temperature from about 22° to 18°C increased the average time to 50% emergence from 106 to 174 hours. The UI averaged 66.3 hours at the lower temperatures and it decreased (seedling emergence was more uniform) to 38.0 hours at the high temperature. Seed vigor had very little effect on UI when the seedlings emerged rapidly, but emergence of seedlings from high seed was more uniform (UI was smaller) than for low-vigor seed when emergence was delayed by low temperatures. Our results are consistent with the definition of seed vigor; high-vigor seed exhibited more uniform emergence than low-vigor seed, but only under stress conditions. Seed vigor had almost no effect on uniformity under ideal conditions.
Seed Technology Newsletter Volume 83, No. 2 19 May, 2009
Identification of Foxtail (Setaria) Impurities: Examination and Comparison of Four Species Jennifer Neudorf and Ruojing Wang National Seed Herbarium, Canadian Food Inspection Agency, Seed Science and Technology Section, 301- 421 Downey Road, Saskatoon, Saskatchewan S7N 4L8, Canada, Email: [email protected]; [email protected]
Abstract Green foxtail (Setaria italica subsp. viridis) and Yellow foxtail (Setaria pumila subsp. pumila) are common impurities in a number of crops throughout Canada. Giant foxtail (Setaria faberi) is an Asian weed that currently grows in South-central Canada. It is currently on the Weed Seed Order (2005) as a Class 1: Prohibited Noxious Species. Knotroot Bristle grass (Setaria parviflora) is a weed found normally in the South-eastern United States (plus California) and may be found in import samples from the southern States and south into South America.
These four species have some similar characters and may be difficult to distinguish. The staff at the National Seed Herbarium have examined these four species and found characters that may aid in distinguishing commonly encountered Setaria species. These characters are typically located on the fertile lemma, the fertile palea and the 2nd, or upper glume. The general shape and size are also important to the correct identification of foxtails.
Table 1. Comparison of Four Foxtail Species Knotroot Bristle Species Yellow Foxtail Green Foxtail Giant Foxtail Grass 2nd - ½ length of the - covers the - ½ - ¾ the - ½ - ¾ the length (Upper) lemma lemma length of the of the lemma Glume lemma - transverse - thin ridges - transverse - transverse ridges remain form a grid ridges diminish ridges remain Lemma thick at tip. pattern at the tip. thick at tip. - three-pronged awn.
- glossy edges - glossy edges - glossy edges - glossy edges Palea covered. exposed. exposed. covered.
- wide elliptical - narrow - wide ovate - narrow ovate shape. elliptical shape. (egg) shape, (egg) shape. strong dip at the - tip of lemma may Notes - 3.0 X 2.0mm - 1.75 X 1.0 mm palea tip. be darkened. - S-shaped side - 2.0 X 1.0 mm view. - 2.5 X 1.5 mm
Seed Technology Newsletter Volume 83, No. 2 20 May, 2009
National Seed Herbarium of Canada Ruojing Wang, Jennifer Neudorf Canadian Food Inspection Agency, Seed Science and Technology Section, Saskatoon Laboratory, 301- 421 Downey Road, Saskatoon, Saskatchewan S7N 4L8, Canada Email: [email protected]; [email protected]
Abstract The National Seed Herbarium (NSH) of Canada contains approximately 20,000 specimens of 14,000 unique species, representing 239 families and 3,279 genera. These seed specimens were collected from international herbaria, government seed laboratories, and botanical gardens. The earliest seed specimen, a sample of Larkspur seed (Delphinium bicolor), dates back to 1869.
Mission • Support a fair and effective regulatory regime in consumer protection in compliance with the Seed Act, Weed Seed Order, Plant Protection Act, and Canada Agricultural Products Act. • Protect the plant resource base by the detection and identification of agricultural weedy species, quarantine pest plant seeds, and invasive alien plant species associated with the Invasive Alien Species Strategy for Canada.
Goals and Objectives • Serve as the national reference and resource centre for seed identification in seed trade certification domestically, regionally and internationally by managing seed specimens, concentrating on economically and environmentally important species. • Identify and verify plant species for seed testing, seed trade certification, agricultural product importation, quarantine, and the detection of invasive alien plant species; • Develop material references, resources and diagnostic methods for seed identification of weedy species and invasive alien plant species using novel information technologies.
Differential Scanning Calorimetry as a Tool for Nondestructive Measurements of Seed Deterioration in Lettuce (Lactuca sativa, CV “Black Seeded Simpson”) Jennifer Crane and Christina Walters USDA-ARS, National Center for Genetics Resource Preservation, Fort Collins, CO 80521
Abstract This study was undertaken to determine if changes in lipid phase behavior could be used to detect lost viability in lettuce (Lactuca sativa) seeds. We used seeds from the cultivar ‘Black Seeded Simpson’ that were purchased every 2-3 years since 1989 and stored in resealable plastic bags at constant 5˚C and relative humidity ranging from 30
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to 60%. Viability of seeds from each harvest year was recently tested by germination assays carried out on two replicates of 50 seeds each, and seed lots were scored for % and rate of germination, physiological necrosis and abnormal development. Seed lipids were extracted from an aliquot of seed from each harvest year and total lipid content and fatty acid composition were measured. The temperature and energy associated with lipid melting were measured using differential scanning calorimetry (DSC) on whole seed and extracted lipid samples from each harvest year. Reduction of normal germination was evident in seeds after 4 years of storage and % germination was less than 20% after 9 years. However, 100% of seeds germinated (radicle emergence) until 13 years of storage and then it dropped precipitously to 0% by year 18. Amount of extractable lipid appeared to decline in seeds with increasing time in storage. In addition, a significant decline in linoleic acid was noticed after 9 years of storage. The energy of the lipid melting transition of intact seed also declined with time in storage and is significantly correlated with reductions in normal germination. The DSC measurements required no special handling protocols and did not affect seed viability or vigor. Hence, it may be a useful, nondestructive tool for determining the progress of seed aging and help schedule actual germination assays for monitor testing.
Cryogenic Storage of Cereal Grains: Results from a 20 Year Experiment Christina Walters, Lana Wheeler, Phil Stanwood USDA-ARS National Center for Genetic Resources Preservation, 1111 South Mason Street, Fort Collins, CO, USA
Abstract This paper compares the viability of small grains stored under conventional (-18oC) or cryogenic conditions (vapor above liquid nitrogen(LN)) for 22 to 25 years at the National Center for Genetic Resources Preservation. Several accessions of different small grains crops were split in 1984-1987, stored at the two temperatures, and assessed for viability in 2003-2008 using standard testing protocols. While some grasses known to have poor shelf life (i.e., Bromus inermis and Lolium multiflorum) showed slightly higher germination percentages after storage in LN compared to -18oC, there were no significant differences between percent germination of most grain species stored under the two conditions. However, grains of Hordeum vulgare, Sorghum bicolor, Triticum aestivum and Zea mays showed lower germination following liquid nitrogen storage compared to -18oC. A more detailed study of T. aestivum grains to determine the basis for this surprising result revealed differences in initial moisture treatments, with -18oC being stored at about 11% water while LN-stored seeds were dried to 7.5% water. This level of drying did not appear to reduce initial germination or cause imbibitional damage, but may have predisposed grains to damage by rapid cooling to LN or overdry storage. Older grains sealed in tubes and placed in vapor above LN (~40oC/min cooling) showed reduced germination compared to the same accessions cooled to vapor phase LN in an insulated container (~1oC/min). Fresh grains showed no sensitivity to cooling rate. We conclude that several variables need consideration when placing cereal grains in LN storage and that overdrying and rapid cooling should be avoided.
Seed Technology Newsletter Volume 83, No. 2 22 May, 2009
Seed Storage Containers: Implications of water permeability properties on moisture management Christina Walters and Lisa Hill USDA-ARS National Center for Genetic Resources Preservation, 1111 South Mason Street, Fort Collins, CO, USA
Abstract Seed moisture must be controlled to maintain high seed quality. Moisture control is accomplished by adjusting or conditioning relative humidity and temperature surrounding the seed. Seeds are packaged in moisture-proof containers to maintain the desired moisture content. The effectiveness of containers as moisture barriers varies with the materials used, and water vapor permeation rates for most materials are known. Specifications when purchasing seed containers should be based on these known water vapor permeation rates as well as the outside environmental conditions and the time that the seed is expected to remain as inventory. While no package is completely moisture-proof, packaging that is highly impermeable to water will help to maintain a near constant seed water content. However, another problem may arise with moisture-proof containers if temperature is not also controlled. Using data loggers, we can demonstrate that relative humidity increases during warming of seed-filled containers and decreases during cooling. Thus, temperature fluctuations can cause fluctuations of relative humidity (RH) within moisture proof packaging. These fluctuations are predicted by water sorption isotherms, which describe temperature-RH- water content interactions within seeds. Elevated RH from warming seeds in sealed bags can cause them to deteriorate faster than expected and reduce the benefit gained from an expensive moisture barrier.
Identification and Characteristics of Solanum, Physalis, Datura, and Quincula species Pattsy Jackson, USDA-AMS-LS-SRTB, 801 Summit Crossing Place, Suite C, Gastonia, NC 28054. (704) 810-8871. [email protected].
Abstract The Solanaceae family consists of about 90 genera and 3000 to 4000 species, and is among the most economically important genera worldwide. This family consists of both crops and weeds, and various species produce edible and poisonous fruits. Due to the global reliance on this family as a food source, it is important to understand seed identification characteristics. This poster will review common seed characteristics of various Solanaceae species and provide readers with proper tools for Solanaceae identification. Many morphological seed characteristics within the Solanaceae family are similar, but hilum, size, shape and seed coat texture can be used to determine differences between species. The seed shape may be oval, circular, C to D shaped and the diameter ranges from 1.5 to 2mm. Seed color is usually uniform, but length of time in a mature fruit and aging can influenced seed color. Although, hilum, shape, texture,
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size and color are the most obvious indicators, analysts should also explore other options, such as knowledge of where the seed was found. This can often significantly narrow the list of species identification. Overall, Solanaceae seeds can be difficult to distinguish, but analysts can examine several seed characteristics for proper identification.
Bonafide BDI® – Rye grass, A Novel, DNA based Diagnostic tool for Adventitious Presence test in Perennial Ryegrass A.C. Chandra-Shekara, Michael Thompson & Pegadaraju Venkatramana* BioDiagnostics Inc, 507 Highland Drive, River Falls, WI-54022 * Presenter: Email:[email protected]
Adventitious presence (unintended presence) of annual ryegrass in perennial ryegrass seed lots causes significant economic losses to the grass seed industry. The International Seed Testing Association (ISTA) recommends the usage of SRF (Seedling Root Fluorescence) and/or grow –out test procedures to estimate the levels of annual rye presence in perennial seed lots. However, both SRF and grow-out tests are labor intensive and time consuming. Furthermore, the SRF test produces inaccurate results and is environmentally influenced. Increasing numbers of perennial seed lots are rejected each year due to the inaccuracy of the SRF test. Thus, there is a clear need for a better testing procedure that could meet the diagnostic needs for ryegrass in an efficacious, rapid and cost effective manner. We have developed a high throughput quantitative PCR (Q-PCR) based diagnostic tool that effectively detects the presence of annual rye grass seed contamination in perennial rye grass lots. The DNA test is designed using an insertion/deletion (In-Del) site in a ryegrass gene involved in regulating the vernalization response of ryegrass. This new DNA test is more sensitive, accurate and cost effective in detecting annual and intermediate type contamination in perennial ryegrass with a high sensitivity of 0.04% in a sample size of 2500 seeds. We have currently validated this method on 68 perennial, 26 annual and 14 intermediate ryegrass varieties with consistent results.
Seed Issues Forum
This dynamic session has become a favorite event at the annual meeting, this year we have a plethora of interesting topics and presentations. These tabletop displays along with the poster presentations represent the cutting edge of seed technology innovation.
• TZ Handbook Revisions, Annette Miller, USDA-ARS-NCGRP • STEP and Seed Images- & Ethan, Waltermire Colorado Seed Lab, Loren Wiesner , USDA-ARS-NCGRP (retired) • Small Seed Legume ID- Brenda Watts, Dairyland Seed Co. • Requirements to Take AOSA Seed Analysts Certification Exam- Mike Gill. New Mexico State Seed Lab
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• Seed Technology Publications Table- Anita Hall, AOSA/SCST • New Vigor Handbook- Dr. Riad Baalbaki, CDFA/PPDC • Seed Technology Journal- Victor Vankus, Chair of Journal Committee, & Dr. Dennis TeKrony, Journal Editor • Introduction to the International Committee- Pat Brownfield, BioDiagnostics West, LLC. • Camelina Germination- Harold Armstrong, Monsanto • PSU of Natives Not In The Rules- Michael Aberle , Ransom Seed Lab • Encrusted Grass Seed Referee- Sharon Davidson, Agri Seed Testing • Table Top Dividing - R. Denny Hall, Wyoming Seed Analysis Lab • Blue Grama Blowing Point Issues - Gil Waibel, Wyoming Seed Analysis Lab • Tall Fescue Blowing Point- Dr. Sabry Elias, PhD, Oregon State University Seed Lab • How Do You Conduct and Report Sand Tests: A Survey- DaNell Jamieson, BioDiagnostics, Inc. • Impact of Maternal Effects on Trait Testing,- Dr. Denise Thiede, BioDiagnostics, Inc. • Seed Vigor Imaging System: A 2 Day Corn Vigor Test - Heidi Larson, Wisconsin Crop Improvement Assoc. • Soybean Virtual Referee- Mike Stahr, Iowa State University Seed Lab • Purity Testing Handbook (draft in progress)- Deborah Meyer, CDFA/PPDC • Characteristics in Identification of Solanum Species- Pattsy Jackson, USDA AMS LS Seed Regulatory and Testing Branch
Workshops at the Annual Meeting
Agenda for the Endophyte Testing Workshop May 31, 2009 Colorado State University
The endophyte work session will be conducted in two parts – one in the morning and one in the afternoon. The morning session will instruct participants how to detect endophyte in seed and stem tissue. Class participants will break out into pairs and work together as a team. Each team will receive two test kits – one for seed analysis and one for grass tiller analysis. The class will go through the process step-by-step so all participants can get practical hands-on experience with endophyte detection. The session will be accompanied by a PowerPoint presentation to explain the significance of endophyte presence in grazing livestock, the conundrum of using endophyte-free seed in pastures, followed by a detailed description on how the immunochemical analysis works. The workshop will provide confidence to participants so they may run the analysis and provide insight towards interpretation of your results. Participants will have a chance to evaluate a new test protocol developed by Agrinostics Ltd. Co. and provide feedback as to which is a superior analysis.
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The afternoon session will focus on alkaloid analysis in seeds and stem tissues for QA/QC of novel (non-toxic) endophyte detection.
Fee: $125 (includes lunch and breaks)
Morning Session:
Welcome, distribution of working materials for endophyte detection 7:45 am teams Getting started – Preparing and placing seed/plant tissues on the test 8:00 am kit format for endophyte extractions and analysis. Beginning the endophyte reaction sequence – how to prepare the extracted samples for analysis. (Blocking and adding mouse 8:45 am antibodies). (Brief PowerPoint presentation to describe what is happening during the first two steps) Continuing with analysis – Washing and adding anti-mouse 9:45 am antibodies. (Continue with PowerPoint presentation) 10:30 am Break (refreshments included) Continuing with analysis – Washing and “Stacking” the antibodies with 11:00 am chromophores (Continue with PowerPoint) 11:45 am The final step – Washing and adding chromogen (color reagent) 12:15 pm Lunch Break Divide into teams of four. Set up extraction of ergot alkaloids from 1:15 pm seed tissues. (PowerPoint explanation on how to set up stem tissue for analysis) Dispensing reagent extracted sample and antibody reagents for 2:00 pm alkaloid analysis in seed (PowerPoint presentation continued) 3:00 pm Break Washing and adding antimouse antibodies with chromophore 4:00 pm (Continued PowerPoint presentation) 5:00 pm Washing and adding color reagent 5:30 pm Interpretation of results. Question/Answers 6:00 pm Soft Drinks, Wine and Cheese – Compliments of Agrinostics Ltd.
Statistics Workshop June 1, 2009 Colorado State University
Experimental Design, Data Analysis, and Tolerances in Seed Testing Fee: $125 (includes lunch and breaks)
The workshop will cover the following topics
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• Quick overview of the principles of experimental design with practical examples • Data Analysis: Analysis of variance (ANOVA); and mean separation • Examples of using statistical packages in analyzing data • Tolerances: What is tolerance? When to use it? How to use tolerances for purity tests, noxious weed seeds, germination, TZ, and moisture?
Instructors Dr. Sabry Elias, AOSA Statistics Subcommittee Chair Dr. Riad Baalbaki, AOSA Germination and Dormancy Subcommittee Chair
Pathology/Genetic Technology Workshop June 1, 2009 Eurofins STA
7:30am Meet in front of Fort Collins Hilton for transportation to Longmont 8:30am Welcome and Introductions – John Mizicko & Darrell Maddox, National Seed Health System & Accredited - 8:45am Lisa Shephard, Iowa State University Seed Science Center 9:15am Set up group rotations 9:30am A-virus, B-mycology, C-bacteria, D-BFB 10:45am A-mycology, B-bacteria, C-BFB, D-virus 12:00pm Lunch 1:00pm A-bacteria, B-BFB, C-Virus, D-mycology 2:15pm A-BFB, B-virus, C-mycology, D-bacteria 3:30pm What is new in seed health testing - Karen McGuire, Envirologix 4:00pm The Accredited Seed Lab program 4:30pm Transportation from Eurofins STA back to Fort Collins Hilton 5:30pm Arrive back at Fort Collins Hilton
Seed Technology Workshop “Publishing Your Seed Research Results in Seed Technology “ Wednesday, June 3 4:00 pm
4:00 p.m. Introductory Remarks, Moderator – Victor Vankus 4:05 p.m. The Nuts and Bolts of Publishing in Seed Technology - Cindy Finneseth 4:30 p.m. Elements of a Scientific Paper (The Abridged Version!) – Riad Baalbaki 5:00 p.m. Panel Discussion – Discussion Leader: Jack Peters Panel: Sue Alvarez, Ken Greger, Jean Tolliver, Loren Weisner
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Topics: Member interest in conducting research and publishing. Barriers to conducting research at the lab. How can associations help? Referee work, rules proposals, and publishing in ST. List of ideas and actions for the future.
5:25 p.m. Closing Comments – Dr. Dennis Tekrony 5:30 p.m. Adjourn
Rocky Mountain National Park Bus Tour all day June 6