ASTM E2610-2018 Standard Test Method for Sensory Analysis&x2014 Duo-Trio Test.pdf

《ASTM E2610-2018 Standard Test Method for Sensory Analysis&x2014 Duo-Trio Test.pdf》由会员分享，可在线阅读，更多相关《ASTM E2610-2018 Standard Test Method for Sensory Analysis&x2014 Duo-Trio Test.pdf（10页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E2610 18Standard Test Method forSensory AnalysisDuo-Trio Test1This standard is issued under the fixed designation E2610; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number in parenthese

2、s indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers a procedure for determiningwhether a perceptible sensory difference exists betweensamples of two products.1.2 This test method appl

3、ies whether a difference may existin a single sensory attribute or in several.1.3 This test method is applicable when the nature of thedifference between the samples is unknown. It does notdetermine the size or the direction of the difference. Theattribute(s) responsible for the difference are not i

4、dentified.1.4 Compared to the triangle test, the duo-trio test isstatistically less efficient, but easier to perform by the asses-sors. For details on how the duo-trio test compares to otherthree-sample tests, see Refs (1-4).21.5 This test method is applicable only if the products arehomogeneous. If

5、 two samples of the same product can often bedistinguished, then another method, for example, descriptiveanalysis, may be more appropriate.1.6 This test method is applicable only when the productsdo not cause excessive sensory fatigue, carryover or adapta-tion.1.7 This standard does not purport to a

6、ddress all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety, health, and environmental practices and deter-mine the applicability of regulatory limitations prior to use.1.8 This international standard was de

7、veloped in accor-dance with internationally recognized principles on standard-ization established in the Decision on Principles for theDevelopment of International Standards, Guides and Recom-mendations issued by the World Trade Organization TechnicalBarriers to Trade (TBT) Committee.2. Referenced D

8、ocuments2.1 ASTM Standards:3E253 Terminology Relating to Sensory Evaluation of Mate-rials and ProductsE456 Terminology Relating to Quality and StatisticsE1871 Guide for Serving Protocol for Sensory Evaluation ofFoods and BeveragesE1885 Test Method for Sensory AnalysisTriangle TestE2262 Practice for

9、Estimating Thurstonian Discriminal Dis-tances2.2 ISO Standards:4ISO 4120 Sensory AnalysisMethodologyTriangle TestISO 10399 Sensory AnalysisMethodologyDuo-TrioTest3. Terminology3.1 DefinitionsFor definition of terms relating to sensoryanalysis, see Terminology E253, and for terms relating tostatistic

10、s, see Terminology E456.3.2 Definitions of Terms Specific to This Standard:3.2.1 (alpha) riskprobability of concluding that a per-ceptible difference exists when, in reality, one does not. (Alsoknown as Type I Error or significance level.)3.2.2 (beta) riskprobability of concluding that no per-ceptib

11、le difference exists when, in reality, one does. (Alsoknown as Type II Error.)3.2.3 pcprobability of a correct response.3.2.4 pd(proportion of discriminators)proportion of thepopulation represented by the assessors that can distinguishbetween the two products.3.2.5 productmaterial to be evaluated.3.

12、2.6 sampleunit of product prepared, presented, andevaluated in the test.1This test method is under the jurisdiction of ASTM Committee E18 on SensoryEvaluation and is the direct responsibility of Subcommittee E18.04 on Fundamen-tals of Sensory.Current edition approved Aug. 1, 2018. Published August 2

13、018. Originallyapproved in 2008. Last previous edition approved in 2011 as E2610 08 (2011).DOI: 10.1520/E2610-18.2The boldface numbers in parentheses refer to the list of references at the end ofthis standard.3For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Custom

14、er Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.4Available from American National Standards Institute (ANSI), 25 W. 43rd St.,4th Floor, New York, NY 10036, http:/www.ansi.org.Copyright ASTM Internatio

15、nal, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United StatesThis international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for theDevelopment of International Standards, Guide

16、s and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.13.2.7 sensitivitygeneral term used to summarize the per-formance characteristics of the test. The sensitivity of the testis rigorously defined, in statistical terms, by the values selectedfor ,

17、, and pd.3.2.8 Thurstonian measure of sensory difference (effectsize) relative to perceptual noise (standard deviation) (seePractice E2262).3.2.9 triadthree samples given to an assessor in theduo-trio test; one sample is labeled as a reference the other twosamples are labeled with different codes. O

18、ne of the codedsamples is the same product as the reference. The other codedsample is different.4. Summary of Test Method4.1 Clearly define the test objective in writing.4.2 Choose the number of assessors based on the level ofsensitivity desired for the test. The sensitivity of the test is, inpart,

19、a function of two competing risks: the risk of declaringthe samples different when they are not (that is, -risk) and therisk of not declaring the samples different when they are (thatis, -risk). Acceptable values of and vary depending on thetest objective and should be determined before the test (se

20、e forexample Appendix X1 and Appendix X2).4.3 Each assessor receives a triad where one sample islabeled as the reference and the other two samples are labeledwith different codes. The assessors are informed that one of thecoded samples is the same as the reference and that one isdifferent. The asses

21、sors report which of the coded samples theybelieve to be the same as (or different from) the reference.54.4 Results are tallied and significance determined by ref-erence to a statistical table.5. Significance and Use5.1 The test method is effective for the following testobjectives:5.1.1 To determine

22、 whether a perceivable difference resultsor a perceivable difference does not result, for example, whena change is made in ingredients, processing, packaging, han-dling or storage; or5.1.2 To select, train and monitor assessors.5.2 The test method itself does not change whether thepurpose of the duo

23、-trio test is to determine that two productsare perceivably different versus that the products are notperceivably different. Only the selected values of pd, , and change. If the objective of the test is to determine if there is aperceivable difference between two products, then the valueselected for

24、 is typically smaller than the value selected for .If the objective is to determine if the two products aresufficiently similar to be used interchangeably, then the valueselected for is typically smaller than the value selected for and the value of pdis selected to define “sufficiently similar.”5.3

25、The test method may change based on the test objectiveor the assessors familiarity with the product. The balanced-reference technique (see 9.1.1) typically is used when neitherproduct is more familiar than the other. The constant-referencetechnique (see 9.1.2) frequently is used when one product is

26、acontrol/current product or is familiar to the assessors.6. Apparatus6.1 Carry out the test under conditions that prevent contactbetween assessors until the evaluations have been completed,for example, using booths that comply with Ref (5).6.2 Sample preparation and serving sizes should complywith G

27、uide E1871. See Refs (6) or (7).7. Assessors7.1 All assessors must be familiar with the mechanics of theduo-trio test (the format, the task, and the procedure ofevaluation). Experience and familiarity with the product andtest method may increase the sensitivity of an assessor and maytherefore increa

28、se the likelihood of finding a significant differ-ence. Monitoring the performance of assessors over time maybe useful.7.2 Choose assessors in accordance with test objectives. Forexample, to project results to a general consumer population,assessors with unknown sensitivity might be selected. Toincr

29、ease protection of product quality, assessors with demon-strated acuity should be selected.7.3 The decision to use trained or untrained assessors shouldbe addressed prior to testing. Training may include a prelimi-nary presentation on the nature of the samples and the problemconcerned. If the test c

30、oncerns the detection of a particulartaint, consider the inclusion of samples during training thatdemonstrate its presence and absence. Such demonstration willincrease the panels acuity for the taint but may detract fromother differences. See Ref (8) for details. Allow adequate timebetween the expos

31、ure to the training samples and the actualduo-trio test to avoid carryover.7.4 During the test sessions, avoid giving information aboutproduct identity, expected treatment effects or individual per-formance until all testing is complete.7.5 Avoid replicate evaluations by the same assessor when-ever

32、possible. However, if replications are needed to produce asufficient number of total evaluations, every effort should bemade to have each assessor perform the same number ofreplicate evaluations.5Organizations differ in the instructions they give their assessors. Someorganizations instruct their ass

33、essors to select the sample that is most similar to thereference. Others instruct their assessors to select the sample that is most differentfrom the reference. Either approach is acceptable.E2610 1828. Number of Assessors8.1 Choose the number of assessors to yield the level ofsensitivity called for

34、 by the test objectives. The sensitivity ofthe test is a function of three values: the -risk, and the -risk,and the maximum allowable proportion of distinguishers, pd.68.2 Prior to conducting the test, select values for , and pd.The following can be considered as general guidelines.8.2.1 For -riskA

35、statistically significant result at:10 to 5 % (0.10 to 0.05) indicates “slight” evidencethat a difference was apparent5 to 1 % (0.05 to 0.01) indicates “moderate” evidencethat a difference was apparent1 to 0.1 % (0.01 to 0.001) indicates “strong” evidencethat a difference was apparentBelow 0.1 % ( 3

36、5 % represent large values8.3 Having defined the required level of sensitivity for thetest using 8.2, use Table A1.1 to determine the number ofassessors necessary. Enter Table A1.1 in the section corre-sponding to the selected value of pdand the column corre-sponding to the selected value of . The m

37、inimum requirednumber of assessors is found in the row corresponding to theselected value of . Alternatively, Table A1.1 can be used todevelop a set of values for pd, and that provide acceptablesensitivity while maintaining the number of assessors withinpractical limits. The approach is presented in

38、 detail in Ref (9).8.4 If one wishes to use Thurstonian as a measure ofsensory effect size, use Tables A2.1 and A2.2 to convertbetween pdand . See Ref (10) for further discussion on therelationship between Thurstonian and pd.8.5 Often in practice, the number of assessors is determinedby material con

39、ditions (for example, duration of theexperiment, number of available assessors, quantity of prod-uct). However, increasing the number of assessors increasesthe likelihood of detecting small proportions of distinguishers.Thus, one should expect to use larger numbers of assessorswhen trying to demonst

40、rate that products are similar comparedto when one is trying to prove they are different. Often 20 to 36assessors are used when testing for a difference. For compa-rable sensitivity when testing for similarity, 40 to 78 assessorsare needed.9. Procedure9.1 If neither product is more familiar than the

41、 other, use thebalanced reference technique (9.1.1). If the product is familiarto the assessors (for example, a control sample from theproduction line), use the constant reference technique (9.1.2).9.1.1 Balanced-Reference TechniquePrepare worksheetsand scoresheets (see Appendix X1) in advance of th

42、e test so asto utilize an equal number of the four possible sequences oftwo products, A and B:ARAB ARBABRAB BRBA9.1.1.1 Distribute these at random among the assessors sothat serving order is balanced.9.1.2 Constant-Reference TechniquePrepare worksheetsand scoresheets (see Appendix X2) in advance of

43、the test so asto utilize an equal number of the two possible sequences of twoproducts, A and B:ARAB ARBA9.1.2.1 Distribute these at random among the assessors sothat serving order is balanced.9.2 Present each triad simultaneously if possible, followingthe same spatial arrangement for each assessor (

44、on a line to besampled always from left to right, in a triangular array, etc.).Within the triad, assessors are typically allowed to makerepeated evaluations of each sample as desired. If the condi-tions of the test require the prevention of repeat evaluations forexample, if samples are bulky, leave

45、an aftertaste, or showslight differences in appearance that cannot be masked, presentthe samples sequentially and do not allow repeated evaluations.In addition, if the samples change over time, for example,chewing gum or cereal with milk, samples should be testedsequentially.9.3 Instruct the assesso

46、rs to evaluate the reference samplefirst and then evaluate the two coded samples in the order inwhich they were presented. The assessor should then indicatewhich of the two coded samples is the same as the reference.9.4 Each scoresheet should provide for a single triad ofsamples. If a different set

47、of products is to be evaluated by anassessor in a single session, the completed scoresheet and anyremaining product should be returned to the test administratorprior to receiving the subsequent triad. The assessor cannot goback to any of the previous samples or change the verdict onany previous test

48、.9.5 Do not ask questions about preference, acceptance, ordegree of difference after the initial selection of the sample thatmatches the reference. The selection the assessor has just mademay bias the reply to any additional questions. Responses tosuch questions may be obtained through separate test

49、s forpreference, acceptance, degree of difference, etc. (see Ref(11).Acomment section asking why the choice was made maybe included for the assessors remarks.9.6 The duo-trio test is a forced-choice procedure; assessorsare not allowed the option of reporting “no difference.” Anassessor who detects no difference between the samples andrequests to report “no difference” should be instructed torandomly select one of the coded samples as being the same asthe reference. In such situations the assessor can indicate thatthe sele