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Tiêu đề Application of Quality Index Method (QIM) Scheme in Shelf-life Study of Farmed Atlantic Salmon
Tác giả K. Sveinsdottir, E. Martinsdottir, G. Hyldig, B. Jỉrgensen, K. Kristbergsson
Trường học University of Iceland
Chuyên ngành Food Science
Thể loại Thesis
Năm xuất bản 2002
Thành phố Reykjavik
Định dạng
Số trang 10
Dung lượng 210,81 KB

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Sensory evaluation

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Sensory and Nutritive Qualities of Food

Application of Quality Index Method (QIM)

Scheme in Shelf-life Study of Farmed

Atlantic Salmon (Salmo salar)

ABSTRACT: Salmon (Salmo salar) was stored in ice up to 24 d, and changes during storage were observed with

sensory evaluation using the Quality Index Method (QIM), and Quantitative Descriptive Analysis (QDA), total viable counts (TVC), hydrogen sulfide (H 2 S)-producing bacteria, and instrumental texture measurements (com-pression test) Maximum storage time in ice was determined with QDA and fat content by Soxhlet extraction A high correlation between QIM and storage time in ice was found Storage time could be predicted with ± 2 d TVC increased exponentially with storage and was dominated by H 2 S-producing bacteria after 20 d in ice, which was the maximum storage time Texture measurements indicated softening of salmon flesh with storage.

Keywords: sensory evaluation, quality of salmon, fish freshness, shelf life

Introduction

FRESHNESS IS ONE OF THE MOST IMPORTANT ASPECTS OF FISH, AND

because of consumer preferences, there is a strong tendency

to select very fresh fish (Luten and Martinsdottir 1997) Sensory

evaluation is the most important method for freshness and

qual-ity assessment in the fish sector (Hootman 1992) The world’s

production of farmed salmon increased between 1990 and 1997,

from 540,000 tons to almost 1,400,000 tons per year (FAO 2000)

In 1997, 38% of the salmon produced in the world was Atlantic

salmon (Salmo salar) Because of the increased trade between

countries, purchases are often performed on unseen lots, and

there is a need for a good freshness grading system for salmon,

such as the Quality Index Method (QIM) This method is a

sea-food freshness quality grading system, which is used to assess

fish freshness in a rapid and reliable way QIM is based upon a

scheme originally developed by the Tasmanian Food Research

Unit (Bremner 1985) The method has to be adapted to each fish

species To date, the system incorporates fresh herring (Clupea

harengus) and cod (Gadus morhua) (Jonsdottir 1992; Larsen and

others 1992), red fish (Sebastes mentella/marinus) (Martinsdottir

and Arnason 1992), Atlantic mackerel (Scomber scombrus), horse

mackerel (Trachurus trachurus) and European sardine (Sardina

pilchardus) (Andrade and others 1997), brill (Rhombus laevis),

dab (Limanda limanda), haddock (Melanogrammus aeglefinus),

pollock (Pollachius virens), sole (Solea vulgaris), turbot

(Scophtal-mus maxi(Scophtal-mus) and shrimp (Pandalus borealis) (Luten 2000),

gilt-head seabream (Sparus aurata) (Huidobro and others 2001), and

farmed salmon (Salmo salar) (Sveinsdottir and others 2001) QIM

has several unique advantages, including estimation of past and

remaining storage time in ice (Botta 1995; Hyldig and Nielsen

1997; Luten and Martinsdottir 1997)

The maximum storage time of fish can be determined by

sen-sory evaluation of cooked samples The Quantitative Descriptive

Analysis (QDA) (Stone and Sidel 1985) is a sensory method,

which may be used for the determination of maximum shelf life

in addition to a detailed description of the sensory profile for a

product With the QDA, all detectable aspects of a product are

described and listed by a trained panel The list is then used to

evaluate the product, and the panelists quantify the sensory as-pects of the product using an unstructured scale The end of shelf life is the result of unpleasant sensory characteristics

most-ly due to bacterial growth The amount of bacteria on newmost-ly caught fish can vary greatly, normally ranging from 102 to 107 cfu/

cm2 (Liston 1980) The most important seafood spoilage bacteria are characterized by their ability to produce H2S and reduce trim-ethylamine oxide (TMAO), which has been used for their specific determination Capell and others (1997) found counts of H2 S-producing bacteria closely associated with the rejection of

sever-al fish species, irrespective of the temperature and atmosphere Microbial metabolites have low odor thresholds, and during fish spoilage, the concentrations of sulfur compounds, short-chain acids, alcohols, sulfur compounds, and amines increase (Olafs-dottir and Fleurence 1997)

In raw fish, the texture softens during chilled storage

(Anders-en and others 1995; Ein(Anders-en and Thomass(Anders-en 1998) because pro-teolytic enzymes break down the muscle structure (Andersen 1995) The fat content of fish flesh appears to influence the tex-ture When the fat content is high, the flesh is softer (Andersen and others 1994), and juiciness increases (Einen and Thomassen 1998) The total lipid content of farmed salmon is often up to double the content found in wild salmon (Moe 1990) and has been reported varying from 12% to 19% (Hafsteinsson and oth-ers 1998; Refsgaard and othoth-ers 1998)

The aim of this work was to perform a shelf-life study with

farmed Atlantic salmon (Salmo salar) and characterize the

chang-es in frchang-eshnchang-ess with the Quality Index Method (QIM) scheme for raw salmon and the Quantitative Descriptive Analysis (QDA) for cooked salmon Furthermore, the goal was to compare the

senso-ry analysis to microbial counts (total viable counts and H2 S-pro-ducing bacteria) and instrumental texture measurements (com-pression test)

Materials and Methods Salmon

The salmon was obtained from the fish farm Silungur ehf

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(Vogar, Iceland) The salmon had been fed various types of the

feed blend “Gull” (Gull 3, 4, 6, 8, 10, 12, depending on the age of

the salmon) from Fodurblandan hf (Reykjavik, Iceland) The

blend contained 40% protein, 16% carbohydrates, and 25% to

30% fat The salmon were starved for 2 wk and then slaughtered

with carbonic acid After slaughtering, the salmon were gutted,

bled, gills cut through, and the salmon were then rinsed in

run-ning water for 30 min, followed by chilling to 0 °C in slush ice (0 to

–1 °C) before icing in boxes The salmon weighed 3 to 4 kg The

fish were slaughtered before sexual maturity in 8 batches

(Octo-ber/November 1999) and stored up to 24 d at 0 to 2 °C in iced

boxes until analyzed A total of 50 salmon were used in the

exper-iment Eleven were used for training the sensory panel Salmon

stored 1, 2, 4, 8, 11, 13, 15, 17, 19, 20, 21, 22, and 24 d in ice were

analyzed during the shelf-life study Three salmon from each

storage day were analyzed with QIM; thereof 2 were used for

QDA, microbial counts, texture measurement, and fat analysis

(Figure 1)

Sensory evaluation

Quality Index Method

The QIM scheme for salmon lists quality attributes for

ap-pearance/texture, eyes, gills, and abdomen and descriptions of

how they change with storage time Scores were given for each

quality attribute according to the descriptions, ranging from 0 to

3 Very fresh fish normally received the score 0, with scores

in-creasing with storage time The scores given for all the quality

at-tributes are summarized by the Quality Index, which increases

linearly with storage time in ice The sensory evaluation of each

attribute was conducted according to Martinsdottir and others

(2001)

Prior to the shelf-life study, the QIM scheme for farmed

salm-on (Sveinsdottir and others 2001) was revised, as it did not

in-clude a parameter for the textural state of rigor mortis

Addition-ally, 1 score was added for color/appearance of the skin Changes

were made in the setup of the scheme and selection of words to

describe the parameters in the scheme, mainly to make each

de-scription more precise and to facilitate the QIM assessment

Twelve trained panelists of the Icelandic Fisheries

Laborato-ries sensory panel participated in the sensory evaluation with

QIM Members had several years of experience in evaluating fish

freshness Prior to the shelf-life study, the panel was trained in

applying the QIM scheme in 2 sessions The scheme was

ex-plained to the panel while observing salmon of different

fresh-ness categories The panel used the scheme to assess 6 to 9

salm-on from 2 to 3 different storage days per sessisalm-on during the

shelf-life study The salmon was placed on a clean table 30 min

before the evaluation The side where the gills had been cut

through was facing down Each salmon was coded with 3 random

digit numbers All observations of the salmon were conducted

under standardized conditions, with as little interruption as

pos-sible, at room temperature, and under white fluorescent light

Quantitative Descriptive Analysis

The QDA, introduced by Stone and Sidel (1985), was used to

assess cooked samples of salmon An unstructured scale (0 to

100%) was used on a list of words describing odor, flavor,

appear-ance, and texture

Twelve panelists of the Icelandic Fisheries Laboratories´

sen-sory panel participated in the QDA of the cooked salmon They

were all trained according to international standards (ISO 1993),

including detection and recognition of tastes and odors, training

in the use of scales, and in the development and use of descrip-tors The members of the panel were familiar with the QDA method and experienced in sensory analysis of salmon Two ses-sions were used for training of the panel using salmon of differ-ent freshness categories Sensory evaluation of the cooked

salm-on was performed parallel to the QIM assessment Each panelist evaluated duplicates of samples from 2 to 3 different storage days The fish was served in a random order during 2 sessions for each day of the sensory evaluation

All sample observations were conducted according to interna-tional standards (ISO 1988) Twelve samples collected from each salmon with skin came from the loin part, ranging from the spine

to 2 cm below the lateral line The samples were coded with 3 ran-dom digit numbers and cooked at 95 to 100 °C for 7 min in a pre-warmed oven (Convotherm Elektrogeräte GmbH, Eglfing, Ger-many) with air circulation and steam and then served to the panel

Microbial counts

Skin samples were collected before all other analysis by cut-ting 2 x 7.5 cm2 skin strips from 1 side of the fish and placed in a Stomacher containing 50 mL Butterfield´s Buffer solution (APHA 1992) Blending was done in a Stomacher 400 for 1 min Flesh samples were collected after QIM evaluation from the other side

of the salmon The skin was washed with alcohol and removed with a sterilized scalpel The flesh under the skin was collected, and after mincing, 25 g were weighed into a stomacher bag con-taining 225 g Butterfield´s Buffer solution to obtain a 10-fold di-lution Blending was done in a Stomacher for 1 min Further 10-fold dilutions were made as needed Total viable counts (TVC) and selective counts of H2S-producing bacteria were done on iron agar (IA) by the pour plate technique with an overlay as de-scribed by Gram and others (1987) The plates were incubated at

22 °C for 3 d Bacteria forming black colonies on this agar produce

H2S from sodium thiosulfate and/or cysteine

Instrumental texture measurements

One sample from each fish was measured in a Texture

Analyz-er (TA.XT2; Stable Micro System, Surrey, England) using a com-pression test The salmon was filleted, skin removed, and sam-ples collected transversely behind the dorsal fin Samsam-ples were cut right above the lateral line, 2.5 cm in length and width, and 2.2 ± 1.4 cm in height The samples were then covered with plas-tic and stored in a refrigerator at 4 to 5 °C until measured (within

3 to 5 h) using an aluminum compression plate (SMSP/100) Samples were compressed to 80% of the sample height at a con-stant speed (0,8 mm/s) with a 100 g concon-stant force The trigger force was set at 5 g and the registration rate to 200 PPS (registra-tions per s)

Fat content

Samples were collected according to a method recommended

by the Norwegian General Standardizing Body or (1994), the Norwegian Quality Cut (NQC) The samples were vacuum packed and stored at –20 °C until analyzed (within 10 d) The fat content was determined with the Soxhlet method (AOAC 1990) with modification described in the IFL´s method manual for chemical analysis (IFL 1999) using the solvent petroleum ether

Data analysis

The QI was treated with analysis of variance (ANOVA, 2-factor without replication) to analyze if a difference existed within a group (QI given for each salmon within a storage day and QI

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giv-Sensory and Nutritive Qualities of Food

en by each judge assessing salmon within a storage day) The

equation of best fit and the correlation coefficients (r) of QI, total

viable count, H2S-producing microbes on salmon skin and flesh,

and instrumental texture parameters against storage time in ice

were calculated using Microsoft® Excel 2000 (Microsoft

Corpora-tion, Redmond, Wash., U.S.A.)

Data from QDA was treated in HyperSense© (Version 1.6;

1996 Icelandic Fisheries Laboratories, Reykjavik, Iceland)

Inter-action of panelists and samples was assumed, and statistical

analysis was performed using 2-factor design with interaction in

the analysis of variance (ANOVA) The program calculates

multi-ple comparison using Tukey´s test Multivariate comparison of

different attributes in QIM and QDA was conducted in the

statis-tical program Unscrambler® (Version 6.1; CAMO, Trondheim,

Norway) with principal component analysis (PCA) Predictability

of QI was analyzed using partial least square regression (PLS)

with full cross validation The average QI for each storage day,

in-cluding assessment of 3 salmon, was used for this analysis The

root mean square error of prediction (RMSEP) was calculated for

the model (the prediction error in original units) Bias is the

aver-aged difference between predicted and measured Y-values for all

samples in the validation set The standard error of performance

(SEP) is the precision of results corrected for the bias From a

PLS2 model, the initial variance (signal) at zero PCs and the

re-siduals variance (noise) after optimal PCs were plotted as a

sig-nal to noise (S/N) ratio for each panelist and for each word (Mar-tens and Mar(Mar-tens 2000) The significance level was set at 5%, if

Table 1—The QIM scheme for farmed salmon Revised from Sveinsdottir and others (2001)

The fish is yellowish, mainly near the abdomen 2

* Examine the side where the gills have not been cut through

Figure 1—Sampling plan for measurements in the shelf-life study of salmon at the Icelandic Fisheries Laborato-ries in November 1999

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not stated otherwise.

Results and Discussion Sensory analysis

Quality Index Method

The sum of scores evaluated according to the QIM scheme

(Table 1) was presented as the Quality Index (QI) The QI was

cal-culated for each storage day of sampling and formed a linear

re-lationship with time (Figure 2)

High correlation between the average QI and days in ice was

obtained with a slope of 0.692 The slope was different from the

slope observed by Sveinsdottir and others (2001) using the QIM

scheme for salmon, presumably because of the revision of the

scheme prior to this shelf-life study, including the addition of 2

score attributes The aim when developing QIM scheme for fish

is to have the regression line begin at the origin (0,0), which was

not reached here, since the intercept was at 1.568 If the line was

forced through the origin, the correlation between the average QI and days in ice became lower (R2 = 0.933) The QIM scheme gave the assessors the opportunity to choose between scores ranging from 0 to 3 but never a negative number, therefore, allowing for residuals above zero but not below

The difference between salmon of the same storage time in ice was in some cases significant The results were analyzed with partial least square regression (PLS) to examine how well the QI could predict the storage time in ice (Figure 3)

The standard error of performance (SEP) value for the QI was 2.0 (Figure 3) The SEP may be used to evaluate the precision of the predictability of the QI Since the QI was the sum of 11 at-tributes evaluated in the QIM scheme, a normal distribution could be assumed (O´Mahony 1986) Esbensen and others (1998) stated that 2*SEP could be regarded as a 95% confidence interval assuming normal distribution Therefore, it can be as-sumed that the QI of a batch (if 3 salmon were assessed) could be used to predict the storage time with ± 2.0 d It could be assumed that including more salmon in the assessment of each batch might reduce this interval, as observed by Sveinsdottir and oth-ers (2001), where including 5 salmon per storage day gave a SEP value of 1.4

There was a variation in the QI obtained by different panel-ists (Figure 4) The variation increased with storage time, indicat-ing that the panelists were in better agreement when analyzindicat-ing very fresh salmon with the QIM scheme at the beginning of stor-age compared to the not-so-fresh salmon at later ststor-ages There was a tendency for some of the panelists to score either higher or lower than the average score obtained throughout the storage time The variation between the panelists in this study, which were trained during 2 1-h sessions, was comparable to the varia-tion between panelists trained during 6 1-h sessions (Sveinsdot-tir and others 2001) in a similar study This indicated that the 2

Figure 2—Quality Index of salmon Averages over each day

of storage analyzed against days in ice.

Figure 3—PLS1 modeling of QIM data from salmon stored

in ice using full cross validation: Measured against

pre-dicted Y values Average QI for each storage day based

on assessment of 3 salmon used to predict storage time

in d.

Figure 4—Average QI of salmon with storage in ice, as given by each panelist (1 through 12)

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Sensory and Nutritive Qualities of Food

sessions were sufficient training for the panel

QIM assumes the scores for all quality attributes increase with

storage time in ice (Figure 5)

The average texture score was determined by pressing a

fin-ger on the spine muscle and observing how the flesh recovered

according to Martinsdottir and others (2001) The scores were

around 0 at storage day 1, as the salmon was in rigor Propagation

of rigor caused the muscle to relax again, and through storage in ice, the flesh became soft due to autolysis influenced by both fish muscle enzymes and microbial enzymes (Gill 1995; Nielsen 1995) The skin became softer or less springy after 17 to 20 d, where the average score increased from 1 to 1.5 The average score of skin odor reached only 2 at the end of the storage time The score 3 (rotten) was used rarely by panelists At the

begin-Figure 5—Average scores of each quality attribute assessed with QIM scheme for salmon stored in ice against days

in ice

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ning of the storage time when the salmon was very fresh, the

odor was described as fresh seaweed or neutral, then a

cucum-ber-like odor dominated the salmon skin odor During later

stag-es, the odor was described as sour and finally as rotten Freshly

caught fish generally contains low levels of volatile compounds

like 2,6-nonadienal, which has a very characteristic cucumber

aroma and a low odor threshold (0,001 ppb), which contribute to

fresh-like odors Short-chain acids, alcohols, amines, and sulfur

compounds from microbial activity probably caused the sour

and rotten odor (Olafsdottir and Fleurence 1997) The average

scores for other quality attributes like skin and all the attributes

for eyes and gills increased throughout the storage time The

av-erage scores for quality attributes of abdomen were very low

un-til after 8 d of storage when they began to increase with the

stor-age time

Quantitative Descriptive Analysis

The positive attributes for flavor of salmon were described as

characteristic salmon, metallic, sweet, and oily flavor on a scale

ranging from 0 to 100% Average scores for most positive flavor at-tributes did not change for the 1st 17 to 19 d of storage but de-creased thereafter (Figure 6) The average scores of sweet and metallic were between 20 and 50 through the storage time, but for salmon stored 21 d, it went below 20 For characteristic salmon flavor and oily flavor, the difference was clearer The scores were between 50 and 70 until 22 d, when they dropped below 40 Scores for the negative attributes, sour, rancid, and musty/ earthy (Figure 6) were low, approximately 0 to 20 for the 1st 17 to

20 d of storage Thereafter, the scores increased, especially sour flavor scores, which were around 50 after 22 d Rancid and musty/earthy flavor reached only 30 after 22 d The feed of farmed salmon often contains carotenoids (Moe 1990), which have been considered to play an important role in protecting

lip-id tissues from oxlip-idation (Burton and Ingold 1984) This may have been the reason for the low rancidity scores The increasing rancid flavor observed during the last storage day might corre-spond to a train-oily flavor reported by Milo and Grosch (1996), who found their nonfresh cooked salmon samples to be fatty and train-oily smelling According to their findings, the rancid flavor

in salmon was caused by formation of volatile oxidation products such as aldehydes and ketones They analyzed various odorants

in salmon of different freshness (stored 26 wk at -60 °C (fresh) and -13 °C (not fresh)) They found propionaldehyde and (Z)-1,5-octadien-3-one as the most potent high-volatile odorants in cooked fresh salmon samples The odor of those compounds was described as sweet and metallic, respectively Odor is a part of the overall flavor, and those compounds may therefore have been responsible for the sweet and metallic flavor of the cooked salmon in this study A mixture of odorants in the cooked salmon might be responsible for the characteristic salmon flavor Milo and Grosch (1996) detected various odorants from cooked

salm-on (fresh), and the characteristic salmsalm-on odor was caused by compounds like propionaldehyde and acetaldehyde (sweet), hexanal and (Z)-3-hexenal (green), methional (boiled potato-like), dimethyl trisulfide (cabbage-potato-like), and 1-octen-3-one (mushroom-like) The oily flavor and odor might have been due

to (Z,Z)-3,6-nonadienal as it was described as fatty and green

Difference for most QDA attributes was generally only ob-served after 20 d in ice (Table 2) Data from day 24 was kept out

Figure 6—Changes in flavor attributes of cooked salmon (average scores) against storage of the raw salmon in ice observed by a trained QDA panel

Figure 7—Loadings in PCA of salmon data including all

quality parameters assessed in QDA of cooked salmon and

storage time in ice f = flavor, o = odor

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Sensory and Nutritive Qualities of Food

of the analysis because the salmon had utterly exceeded the

lim-its of acceptance When the salmon had been stored for 21 d in

ice, a part of the panel refused to taste the samples after

smell-ing the salmon This strongly indicated that after 20 d of storage

in ice, salmon was—according to sensory evaluation—no longer

fit for human consumption This was in agreement with previous

studies Sveinsdottir and others (2001) concluded that 20 to 21 d

was the maximum storage time in ice for salmon Magnussen and

others (1996) observed sensory changes in cooked salmon stored

7, 14, and 21 d and found minor differences between 7 and 14 d,

but the overall quality was greatly reduced after 21 d of storage

Lande and Rørå (1999) analyzed the flavor, odor, and overall

ef-fects in cooked salmon Minor changes were observed with

stor-age time up to 18 d in ice, however, they did not continue the

sensory evaluation of cooked salmon after the 18 d

Differences were observed among panelists for each QDA at-tribute This is a well-known phenomenon in sensory evaluation The main types of differences among assessors may be caused

by confusion about attributes, individual differences in sensitiv-ity to certain sensations, individual differences in the use of the scale, or individual differences in precision (Næs and others 1994) Various ways have been discussed to detect and handle such differences among assessors (Næs 1990; Næs and Solheim 1991; Næs and others 1994) The noise to signal ratio may be ob-served to decide how to treat the difference among assessors (Sveinsdottir and others 2001)

When the results were analyzed with PCA, the variable d in ice contributed to PC1, and a clear grouping was found between positive and negative sensory attributes on each side of the PC1-axis (Figure 7) Negative parameters became more evident in

Figure 8—Total viable count and H 2 S-producing microbes on skin and in flesh of salmon stored in ice

Figure 9—Correlation between bacterial counts on skin and Quality Index of salmon stored in ice

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salmon stored longer in ice as they were grouped with the

param-eter d in ice, while the positive paramparam-eters became less evident

The negative attributes described salmon at the end of the

stor-age time similarly Discoloration appeared to become slightly

more evident with storage, but the texture parameters evaluated

in cooked salmon contribute very little to PC1 and therefore do

not appear to change with storage time, contrary to the texture of

raw salmon

Microbial counts

The total viable counts (TVC) on skin and in flesh increased

exponentially with storage time (Figure 8) A similar pattern was

noted for bacterial counts on skin and QI with storage time, as

salmon of low bacterial counts also received low scores in QIM A

high correlation was established between QI and TVC on skin,

and the same was seen for H2S-producing bacteria, which

in-creased proportionally to the TVC at the later stages of storage

(Figure 9)

At the beginning of storage, the TVC on skin was

approxi-mately 103 cfu/cm2, which is not unusual for newly caught fish

(Liston 1980) Very few H2S-producing microbes were a part of the

initial microflora (< 10 cfu/cm2), but their proportion of the TVC

increased with storage time The TVC (mainly H2S-producing

mi-crobes) on salmon skin was 108 cfu/cm2 after about 20 d of

stor-age The bacterial counts in salmon flesh were lower than those

on the skin Newly slaughtered salmon contained TVC around 10

cfu/g in flesh The flesh of healthy live or newly caught fish is

sterile because the immune system of the fish prevents the

bac-teria from growing in the flesh, but when the fish dies, the

im-mune system collapses, and during storage, bacteria invade the

flesh (Gram 1995) After 20 d of storage in ice, the TVC was 105

cfu/g As for the microbial growth on salmon skin, the H2

S-pro-ducing bacteria dominated the bacterial flora at the end of stor-age Counts of H2S-producing bacteria were very low (below 10

Figure 10—Typical compression curve of the instrumental texture measurements of a salmon sample in the shelf-life study, measured in the TA.XT2 Texture Analyzer (SMS) Hardness = H1, Resilience = A2/A1, where H1 equals the maximum force, A1 equals the area under the curve from

b e g i n n i n g o f m e a s u r e m e n t u n t i l m a x i m u m f o r c e i s reached, and A2 equals the area under the curve from maximum force until the force has reached zero again.

Table 2—Sensory scores of attributes of cooked salmon assessed by QDA

in ice flavor (+) flavor (+) flavor (+) flavor (-) flavor (+) flavor (-) Juicy Te n d e r

21

22

Statistical analysis of QDA scores of cooked salmon using 2-factor design with interaction ANOVA and Tukey’s test for multiple comparison showing the

storage day when difference is significant ((+) indicate positive attributes and (-) negative attributes.)

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Sensory and Nutritive Qualities of Food

cfu/g) until after 8 d in ice Similar results were observed and

re-ported by Lande and Rørå (1999) The TVC in salmon flesh at the

rejection limits observed in this study were considerably lower

than what has been found previously (Olafsdottir and others

1997) This could be caused by the high counts of H2S-producing

bacteria at the end of the storage time, since those organisms

were probably primarily responsible for spoilage (Capell and

others 1997) This supports the rejection of the cooked salmon

samples after 20 d of storage, when the TVC were dominated by

H2S-producing bacteria

Instrumental texture measurements

The instrumental hardness (Figure 10) of salmon samples

de-creased with storage time (Figure 11), indicating softening of the

salmon flesh Similar results were observed by Andersen and

others (1995) and Einen and Thomassen (1998)

There was no correlation between texture parameters

evalu-ated in cooked salmon and instrumental texture parameters for

raw salmon (Table 3) This was not unexpected for juiciness, as

none of the measured texture parameter simulates juiciness

However, tough/tender might have been related to instrumental

factors such as the attributes hardness and resilience, expressing

how stretchable the samples were The texture evaluated in QIM

(stiffness), on the other hand, was correlated to instrumental

tex-ture parameters Salmon with firm textex-ture according to

instru-mental texture measurements was assessed firm in QIM

Fat content

The average fat content of the salmon was 15.1 ± 2.1% (95%

confidence interval) and ranged from approximately 10% to 19% This was comparable to previously reported fat content of farmed salmon (Hafsteinsson and others 1998; Refsgaard and others 1998)

Tenderness, rancid odor, and flavor increased with increased fat content of the salmon (Table 4) Tenderness has previously been reported to increase with increased fat content in salmon (Andersen and others 1994) Juiciness did not correlate with fat content

Conclusions

THE SCORES FOR QUALITY ATTRIBUTES INCLUDED IN THE QIM scheme increased differently with storage time in ice, but a linear relationship with high correlation was found between QI and storage time in ice Individual salmon spoil at different rates A minimum of 3 salmon should be included in the assess-ment of each batch of salmon The storage time of the salmon may be predicted within ± 2.0 d at the 95% significance level, but examining a greater number of salmon per batch might increase the precision Based upon the sensory evaluation of cooked salmon, the maximum storage life of salmon has been deter-mined as 20 d in ice The quality of the cooked salmon did not change much through ice storage until 17 to 20 d Then the scores for positive attributes decreased, while the scores for neg-ative attributes increased Differences among panelists were evi-dent for all evaluated attributes in QDA and the QI The high cor-relation between QI and storage time in ice made it possible to predict the past storage time in ice As the maximum storage time

of salmon in ice was determined as 20 d, this information may be utilized directly for assessment with the QIM for farmed salmon

to predict remaining storage time in ice assuming optimum stor-age conditions and used in production and quality manstor-age- manage-ment

References

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0802-3220, ISBN 82-575-0265-0 P 1-37.

Andersen UB, Strømsnes AN, Steinsholt K, Thomassen MS 1994 Fillet gaping

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MS 20010283 Submitted 6/1/01, Accepted 9/7/01, Received 12/20/01 This work was carried out at the Icelandic Fisheries Laboratories (IFL) as a part of an ongoing project called Quality Index Method and Information Technology (QimIT) (CRAFT, CT97 9063) The authors would like to thank Asa Thorkelsdottir and the sensory panels at IFL, staff at the service department for microbial and chemical analysis, and Gudrun Olafsdottir and Rosa Jonsdottir for advice.

Authors Sveinsdottir, Martinsdottir, and Kristbergsson are with University

of Iceland, Dept of Food Science at Icelandic Fisheries Laboratories, Icelan-dic Fisheries Laboratories, P.O Box 1405, Skulagata 4, IS-121 Reykjavik, Iceland Authors Hyldig and Jørgensen are with Danish Institute for Fisher-ies Research, Technical Univ of Denmark, Build 221, DK-2800 Lyngby, Denmark Direct inquiries to author Kristbergsson (E-mail: kk@hi.is).

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