Sensory Defects of Virgin Olive Oil From A Microbiological Perspective
Sensory Defects of Virgin Olive Oil From A Microbiological Perspective
Sensory Defects of Virgin Olive Oil From A Microbiological Perspective
5
6 Virgin olive oil is the juice from the olive drupe, a produce that usually features high
7 quality. However, virgin olive oils produced in different regions of the world suffer from
8 defects, most of them of sensory nature. The largest amount of olive oil in which some
9 organoleptic defect is present matches to the Virgin Olive Oil (VOO) class. The causes
10 leading to sensory defects in virgin olive oil, on the different steps of the elaboration, are
11 not well-known sometimes. Important is to note that current legislation allow the
12 classification with sensory defects as VOO and Lampante Olive Oil (LOO). Volatile
13 compounds are important in the sensory perception of the olive oils, for both the positive
14 attributes and the defects. Knowledge on the biogenesis of the volatile compounds involved
15 in the virgin olive oil defects and in its sensory characterisation, is still scarce. There are
16 different causes of defects, depending on the physical, chemical or microbial degradation
17 affecting the product. These join to the positive attributes, leading to an infinite diversity of
18 sensory 'fingerprints'. The microbes cause the most of the defects sensory analysed in olive
19 oils. Despite some interesting studies reported on the biogenesis of the compounds
20 responsible of such defects, microbiological research within the olive oil production,
21 including post-harvest life of olives, is scarce. We should highlight there is a long way to
22 avoid the generation of sensory defects in olive oils within the production process itself and
23 storage. This paper tries to identify significant shortfalls on the knowledge of the causes
24 and circumstances for inducting sensory defects in olive oils, and defining the major
25 aspects which are sufficiently known.
27 Introduction
28 The mechanical procedures for elaborating oil from olives are different from those usual for
29 preparing natural fruit juices. In fact the chemical constitution of these latter is mostly the
30 watery solution of sugars, organic acids and pigments, whereas olive oil is mainly lipid.
31 Overcoming these differences, the nature of olive oil is also the natural juice of the fruit’s
32 mesocarp, different to that of seed oils (Salas, Harwood & Martínez, 2013). Virgin olive oil
33 is obtained through physical methods where the rules prohibit the use of solvents
34 (International Olive Council, 2009), while it is the major method used for oilseed extraction
35 (Rosenthal, Pyle & Niranjan, 1996). The olive oil which fulfils the conditions for direct
36 marketing is classified as Virgin Olive Oil (VOO) or Extra Virgin Olive Oil (EVOO). Such
37 olive oils must be of high or acceptable quality, both on their sensory and physic-chemical
38 characteristics.
39 Olive oil is composed mainly of a saponifiable fraction accounting for 98.5-99.5% weight.
40 This is formed by a lipid matrix of triglycerides, diglycerides and monoglycerides, these
41 last two with about only 1.5% only of total fatty acids (Civantos, 1999a). Olive oil fatty
42 acid composition is characterized by oleic acid as major part, providing a high
43 monounsaturated-to-polyunsaturated fatty acid ratio, and it’s also the major cause for the
44 oil oxidative stability (Velasco & Dobarganes, 2002). Second, it contains a pool of minor
45 but important compounds among lipids, such as phytosterols, waxes, carotenoids,
46 tocopheroles and other as pentacyclic triterpenes. Squalene, an aliphatic hydrocarbon, is
47 also in relatively high quantities within the minor component fraction, as well as
48 compounds quite soluble in water like polyphenols, which stand out by its powerful
49 antioxidant activity. Chlorophylls, aliphatic alcohols and terpenic alcohols are also present
50 (Civantos, 1999a). We must remember that olive oil is not free from moisture, which can
51 be up to 0.1%, playing an important role in developing microbial changes.
52 The current standards fixed by the International Olive Council differ slightly from that of
53 the European Union (EU), the largest olive oil producer in the world, accounting for more
54 than 80% (International Olive Council, 2015). In the EU (European Comission, 1991) the
55 Standard needs for EVOO the presence of the fruity attribute and the complete absence of
56 sensory defects, and other physic-chemical characteristics such a free acidity below 0.8%.
57 In contrast, the VOO admits the presence of sensory defects below 3.5 on a scale of 10, and
58 2 % maximum acidity.
59 Those olive oils in which the sensory analysis decides the absence of fruity or/and the
60 presence of sensory defects whose intensities exceed the value 3.5, classifies as Lampante
61 Olive Oil (LOO). Thus, they must undergo refining, getting Refined Olive Oil (ROO).
62 These olive oils are not edible, but only after mixing them with EVOO or VOO and
63 classifies us Olive Oil (OO). OO may be manufactured as specific mixtures or 'coupages',
64 which manufacturers produce according to the market.
65 EVOO is the most reputable olive oil. There is little information on the world production of
66 the different categories of olive oils, especially in the case of LOO. Spain, the most
67 important olive oil producer in the world, yields around 45% according the information
68 available from the International Olive Council (2015). For this, we will use the production
69 of Spanish olive oil as an example. The quantities of LOO and VOO vary over different
70 seasons, as shown in Table 1. The sum of both classes varies in Spain from 45% to 55% of
71 the total olive oil, the same in which sensory defects are present in greater or lesser extent
72 depending on the produce. The data are elaborated from the Statistical Yearbook of the
73 Spanish Ministry of Agriculture during the period 1980-2009 (Ministry of Agriculture,
74 1980-2009). In 2008 LOO represented 12% of the total Spanish olive oil, while in 2011 it
75 was the significant amount of 23.5%. Nevertheless, the sum VOO+LOO was 55% of the
76 total production in both years.
77 Table 1
78 We must highlight that LOO represents cases of very poor quality. The absence of the
79 fruity attribute, the marked sensory defects, and the acidity above 3.3% are overall signs of
80 great fruit or produce damage at any point in the olive oil elaboration. Nevertheless the
81 largest amount of olive oil with some degree of sensory defect, until 3.5 of maximum
82 intensity, matches to the VOO class. For the Spanish production, VOO accounts a yearly
83 average around 40% of the total (Table 1).
84 The current legislation defines the classification and determines the quality of all olive oils
85 commercially available. A part of this shows some intensity of sensory defects, as for
86 VOO. Trading LOO occurs only within the industry, and its intensity of defects is higher
87 than 3.5. The quantities of olive oil of different classes do not belong to the realms of
88 Science but to Statistics. They provide a message of extraordinary importance: an
89 outstanding percentage of the olive oil production has a certain intensity of defects, most of
90 them of sensory nature. This is well known by experts in the olive oil industry, and we
91 believe this data justifies the present work. The implicit message goes further if we try to
92 answer the following question in detail: What are the causes and circumstances leading to
93 sensory defects in olive oil? The answer is sometimes only loosely known. The purpose of
94 this paper is to help defining what are known enough, defining aspects suffering from
95 significant shortfalls, on the knowledge about the causes and events inducting sensory
96 defects in olive oils.
98 Olive oil sensory quality is described mainly according to volatile compounds, whose
99 detailed description was reported recently (Aparicio, Morales & García 2012). Around one
100 hundred and eighty compounds, were found to be responsible of virgin olive oil aroma
101 (Olías, Del Barrio & Gutiérrez, 1977; Del Barrio, Gutiérrrez & Gutiérrez, 1981; Morales,
102 Aparicio & Ríos, 1994; Angerosa, 2002; Procida, Giomo, Cichelli & Conte, 2005; Morales,
103 Luna & Aparicio, 2005). Thereby, specific relations between volatile compounds and
104 sensory attributes and defects of olive oils have been established. Volatiles can be formed
105 and then released from the olive oil matrix, but they can be native components too
106 remaining within the product (Schreider, 1984), and participating not only in olive oil
107 odour but also in its flavour.
108 There is also a part on olive oil flavour which is not due to volatile compounds. This is the
109 case of the ‘bitter’ and ‘pungent’ attributes, two components that can clearly emphasise the
110 flavour of many types olive oils which contribute positively to the sensory quality
111 (International Olive Council, 2013a). Oleuropeine and its aglycon form are especially
112 responsible, among the phenolic compounds, for the bitterness of virgin olive oils (Caponio,
113 Gomes, & Pasqualone, 2001). While, oleacein and oleocanthal are responsible for the
114 burning pungent sensation of certain olive oils (Andrewes, Busch, De Joode, Groenewegen,
115 & Alexandre, 2003). These attributes, however, are not of much consideration in the
116 commercial standard, since they are not decisive in olive oil classification. Many other
117 attributes are named by their likeness to different flavours in which ingredients other than
118 volatile compounds are present. Such are the cases of fresh herb, apple, white fruit, green
119 fruit, nutty, almond, or tomato.
120 The knowledge on the biogenesis of the volatile compounds that participate in olive oil
121 sensory quality is little, despite the existence of important research (Olías, Del Barrio,
122 Gutiérrez, 1977; Olías, Pérez, Ríos, & Sanz, 1993; Luaces, Pérez, & Sanz, 2003; Angerosa,
123 Servili, Selvaggini, Taticchi, Esposto, & Montedoro, 2004; Sánchez-Ortiz, Pérez, & Sanz,
124 2007; Sánchez-Ortiz, Pérez, & Sanz, 2013; Reboredo, González, Cancho, & Simal, 2013).
125 Green odour biogenesis of some virgin olive oils has been studied, leading to a possible
126 pathway for the C6 polar volatile compounds. According to this route, a lyase would cleave
127 the 13-hydroperoxides (C13-OOH) of linoleic and linolenic acids to form the volatile
128 aldehydes hexanal and cis-3-hexenal, respectively. This pathway involves other enzymes
129 such as acyl hydrolase, lipoxygenase, hydroperoxido lyase, alcohol dehydrogenase and
130 alcohol acetyl transferase (Olías, Pérez, Ríos & Sanz, 1993; Kalua, Allen, Bedgood,
131 Bishop, Prenzler & Robards, 2007).
132 Short chain alcohols present in olive oil aroma are responsible for its characteristic and
133 appreciated ‘green notes’. Salas & Sánchez (1998) suggested that these short chain alcohols
134 are formed from the aldehydes by a NADP-dependent alcohol dehydrogenase (ADH)
135 present in the mesocarp of developing olives. This points the relation between the alcohol-
136 dehydrogenases of olive fruit and the volatile’s biogenesis.
137 A study on the lipoxygenase activity within the olive fruit development have revealed its
138 significance in the biosynthesis of virgin olive oil aroma. It was reported that olives showed
139 the highest lipoxygenase activity about 15 weeks after anthesis, with a steady fall during
140 the growth and ripening periods (Salas, Williams, Harwood & Sánchez, 1999). From here,
141 those authors proposed that olive lipoxygenase engages in the biogenesis of six-carbon
142 volatile aldehydes. The same authors highlight that six-carbon volatile aldehydes are major
143 constituents of the aroma of virgin olive oil during the extraction. Modulating the aroma’s
144 biogenesis produced from the alcohol- dehydrogenase of Olea europaea in the fruit is other
145 interesting aspect that has been described (Iaria et al. 2012). Characterising the
146 lipoxygenases has been further studied in some olive cultivars, showing again their role in
147 the synthesis of volatile compounds (Ridolfi, Terenziani, Patumi & Fontanazza, 2002). The
148 enzyme alcohol acyltransferase from olive fruit has been characterised too (Salas, 2004).
149 Sánchez-Ortiz, Pérez & Sanz (2007) reported cultivar differences on non-esterified
150 polyunsaturated fatty acids as a limiting factor for the biogenesis of virgin olive oil aroma.
151 Also, Salas & Sánchez (1999) identified the inactivating of hydroperoxide-lyase by
152 malaxation at temperature high as cause of drop of the flavour of virgin olive oil. The role
153 of the olive seed in the biogenesis of virgin olive oil aroma is an interesting issue. Olive
154 seeds would afford an alcohol acyltransferase that might be unspecific for substrate,
155 producing any kind of esters (Luaces, Pérez & Sanz, 2003). Further, the role of the pulp and
156 seed in the biogenesis of extra EVOO aroma through the lipoxygenase (LOX) pathway has
157 been studied in four cultivars (Arbequina, Picual, Local and Manzanilla de Sevilla). C6 and
158 C5 volatile compounds were revealed responsible for EVOO aroma, which were produced
159 by endogenous enzymes in both parts of olive fruits. It was shown that these compounds
160 have mainly their biogenesis in the pulp (80–90%) instead of in the seed (20–10%),
161 independently of the cultivar considered (Reboredo, González, Cancho & Simal, 2013).
162 The second essential part of the sensory quality of olive oil is the sensory defects. The
163 different types of sensory defects of olive oils are in the quality standards of both the EU
164 and the International Olive Council. There are different causes of defects, depending on the
165 physical, chemical or microbial degradation of the product. Such degradations may occur
166 concomitantly, inducing a set of chemical and sensory negative attributes, which together
167 with positive ones leads to an infinite diversity of sensory fingerprints of the virgin olive
168 oils.
169 The main defects that can be detected in certain olive oils, from the highest to the lowest
170 frequency, are the following. Fusty flavour develops when olives are stored in piles,
171 favoring anaerobic fermentation. Mouldy is characteristic of olive oil got from wet olives,
172 stored for days, in which fungi and yeast have developed. Muddy sediment defects appear
173 when the olive oil has been in contact with the sediment in vats or tanks. Winey-vinegary is
174 characteristic of certain olive oils with wine or vinegar flavour, due to the fermentation
175 responsible for producing acetic acid, ethyl acetate and/or ethanol. Rancid flavour is
176 characteristic of olive oil that has undergone oxidation, with full correlation between the
177 intensity of the defect and the degree of oxidation. Metallic comes from prolonged contact
178 with metallic surfaces during crushing, mixing, pressing or storing. Heated or burnt
179 attributes are usually due to excessive and/or prolonged heating during processing,
180 especially in the thermo-mixing of the dough. Alpechin is the olive oil flavour received by
181 prolonged contact with vegetable water. Other defects are hay-wood, due to dry olives and
182 brine, typical of olive oils extracted from olives with brine conservation. Earth, is typical of
183 olive oils got from fruit that have been in contact with the earth or mud or improperly
184 washed. There are also defects that occurs rarely, as the lubricant flavour, reminiscent of
185 diesel, grease or mineral oil and whose origin would likely be the contact with lubricants
186 extraction machinery.
187 One relevant facet on olive oil sensory defects concerns to fatty acid alkyl esters (FAAEs).
188 FAAEs originate by esterification of free fatty acids with short chain (from one to four
189 carbon-atom) alcohols, mainly methanol and ethanol yielding methyl and ethyl esters,
190 respectively (Gómez-Coca, Moreda, & Pérez-Camino, 2012). When FAAEs are present at a
191 certain concentration, the fermentative change becomes clear (Pérez-Camino, Moreda,
192 Mateos & Cert, 2002). From here, a relationship between FAAEs concentration of olive
193 oils and its fermentative sensory defects have been established, as well as with their sensory
194 classification (Gómez-Coca, Moreda, & Pérez-Camino, 2012). The esterification needs the
195 presence of short chain alcohols produced by fermentation and olive oil free fatty acids,
196 according to the same authors.
197 The adoption of the FAAEs as quality parameter to classify olive oil either as virgin or
198 extra virgin took place some years ago (International Olive Council, 2010; European
199 Commission, 2011). However, today the relationship between FAAEs and some sensory
200 defects, and the convenience of the current limits, are questioned. Therefore, in 2013 new
201 official requirements were established, the FAAEs maximum allowed limit reduced to 40
202 mg.kg-1. Additionally, decreasing such threshold 5 mg.kg-1 by year within the two
203 following, was scheduled (International Olive Council, 2013b; European Commission,
204 2013). Rapid methods for predicting sensory defects have been reported (Sinelli, Cerretani,
205 Egidio, Bendini, & Casiraghi, 2010; Lerma-García, Cerretani, Cevoli, Simó-Alfonso,
206 Bendini, & Toschi, 2010; Cayuela, Peña, & García, 2013). These technologies, different to
207 the insight above, would be useful to prevent mixing batches of defective virgin olive oils
208 with those without specific quality problems.
209 The volatiles involved in the major defects of virgin olive oil have been described by
210 several authors (Del Barrio, Gutiérrez & Gutiérrez, 1981; Procida, Giomo, Cichelli &
211 Conte, 2005; Morales, Luna & Aparicio, 2005; Aparicio, Morales & García 2012). Most of
212 them are due to microbes. The driving force in the research above is revealing the enzymes
213 forming the characteristic volatiles of defective olive oils (Angerosa, Lanza & Marsilio,
214 1996; Angerosa, Lanza, D'Alessandro, Marsilio, & Cumitini, 1999; Olías, Pérez, Ríos, &
215 Sanz, 1993;Sánchez-Ortiz, Pérez, & Sanz, 2007). It is important considering whether they
216 come from the olive or they are produced by microorganisms, which generally has not so
217 far been the main objective in these studies.
218 Each of muddy, mouldy, fusty and vinegary flavours involves many volatile compounds.
219 These are different depending on the produce, according to several authors (Angerosa,
220 Servili, Selvaggini, Taticchi, Esposto, & Montedoro, 2004; Aparicio, Morales, & García-
221 González, 2012; Gutiérrez, Dobarganes, Gutiérrez, & Olías, 1981; Morales, Luna, &
222 Aparicio, 2005; Olías, Del Barrio, & Gutiérrez, 1977). Some of them highlight by their
223 quantitative importance, according a summary (Table 2) of data reported by Procida,
224 Giomo, Cichelli & Conte (2005), referencing to several studies which have been previously
225 reported.
226 The vinegary pattern is a special case since acetic acid and ethylacetate accounts much than
227 70%. Ethanol and methanol, respectively responsible for some 16% and 5% of the total
228 composition of volatile in this olive oil pattern, are also important. The fusty pattern
229 includes mainly ethanol (38%), octane (14%), ethylacetate (12%) and methanol (11%). In
230 the muddy pattern highlights ethanol (30%), and in proportions between 10% and 5%
231 butylformate, ethylacetate, 2-butanol, 1-propanol and ethylpropionate (Procida, Giomo,
232 Cichelli & Conte, 2005).
233 The volatile compounds total in the mouldy pattern is less than in the remaining major
234 defects, according the same data. In this, ethanol and hexanal, represents about 20% of the
235 total, methanol around 12% and in proportions between 4 and 10% propanal, pentanal and
236 propylpropionate. Moreover, in this pattern none volatile represents much more than 20%
237 of total among 38 detected compounds. Important is highlighting that in many cases,
238 compounds of very low concentration are major responsible for the defect, as can be in the
239 mouldy flavour. Thus, compounds with high odour threshold values have less sensory
240 significance than those with low odour thresholds (Luna, Morales & Aparicio, 2006). The
241 odour activity values (OAVs) of volatile compounds, defined as the ratio of the
242 concentration to the odour threshold, is used to define their sensory significance (Rothe &
243 Thomas, 1963; Aparicio & Morales, 1998; Buettner & Schieberle, 2000). The off-flavour
244 compounds are potentially toxic and have low odour thresholds (Angerosa, 2000).
245 However, we have to underline that beyond its organoleptic significance, the data included
246 in Table 2 signal the origin of the sensory defects that is more important for our current
247 purpose.
248 In this sense, we must highlight the quantitative importance of ethanol in muddy, mouldy,
249 fusty and vinegary flavours. Methanol as well is present in the last three, and it is noticeable
250 that its odour threshold in olive oil has not been reported. Both volatile reveals a
251 remarkable influence of the alcoholic fermentations in the sensory defects most normal in
252 the virgin olive oils. Worth to note this can have a direct relation with yeast fermentations,
253 produced at any point of the manufacturing or storage.
254 Table 2
256 One of the facets of olive oils’ sensory defects known worst is what are the circumstances
257 leading to producing undesirable flavours from microbial causes, within the virgin olive oil
258 extraction. The fusty, mouldy, winey-vinegary, and muddy sediment are in fact caused by
259 microbes. Moreover the basic defects mentioned above are recognised as families of
260 defects, which show some overlap. The storage of olives in piles induces fermentation
261 which can carry into dramatic sensory defects. The biogenesis of fusty defect has been
262 studied by chemical and microbial analysis in olives stored in piles and their resulting olive
263 oils (Gutiérrez, R., Dobarganes, M.C., Gutiérrez, F., & Olías, J.M. (1981). The quali-
264 quantitative composition of the olive oil volatile fraction was reported as good marker of
265 some metabolites produced by microorganisms involved during the fruit storage (Angerosa,
266 Lanza & Marsilio, 1996). The above authors indicated that some volatile compounds, such
267 as 2- and 3- methyl butan-1-al, their corresponding alcohols and propionic acid, 2-methyl
268 propionic acid and 3-methyl butanoic acid, are produced. It was observed in the same study
269 a dramatic development of Clostridium sp. and in a lower proportion, of Pseudomonas sp.,
270 which produce branched aldehydes, branched alcohols and their corresponding acids,
271 surpassing in a few days the threshold levels for sensing fusty defect (Angerosa, Lanza &
272 Marsilio, 1996). The possible presence of Acetobacter is responsible, according the same
273 authors, for the vinegary defect because of producing acetic acid. Besides, softening fruits
274 during the storage has been attributed by the same authors to moulds and other
275 microorganisms in rapid growth belonging to Enterobacter sp.
276 Angerosa, Lanza, D'Alessandro, Marsilio, & Cumitini (1999) studied the modifications of
277 volatiles in virgin olive oils by Aspergillus parasiticus and Penicillium nalgioviense,
278 responsible for musty defect. For this purpose, the above authors compared the volatiles of
279 olive oil samples from fresh fruits with those oils extracted from olives inoculated with
280 mould cultures. Their results point out that trans-2-hexenal disappears, as well as the
281 presence of 3-octanol and 1-octen-3-ol, typical metabolites of the inoculated cultures.
282 Meanwhile, yeasts can produce great amounts of ethanol and ethyl acetate, especially with
283 temperature warm, inducing the winey defect (Angerosa et al., 2004). Interesting results
284 were reported by Fakas et al. (2010), which focused on characterising olive fruit microflora
285 and its influence on olive oil volatile compound biogenesis. Olive fruits of the Greek
286 variety ‘Amfissis’ were stored under industrial conditions, its microflora isolated and
287 identified. The above authors selected moulds, and screened it for production of lipase and
288 lipoxygenase. These last are two enzymes known to act during the biogenesis of olive oil
289 aroma through the lipoxygenase pathway. A Penicillium strain was identified as the most
290 potent enzyme producer, and its production of lipase and lipoxygenase quantified. The
291 authors reported that olive microflora can contribute to the biogenesis of olive oil volatile
292 compounds. Thus, some of its members could potentially be used to increase the olive oil
293 aroma.
294 For understanding why the microorganisms are involved in the olive mill scene, we should
295 point out that a few decades ago it was still frequent storing the olives in large lashings. The
296 cause was they were waiting the moment of grinding, because of the mills’ limits in
297 particular areas (Gutiérrez, R., Dobarganes, M.C., Gutiérrez, F., & Olías, J.M., 1981).
298 Currently the waiting time depends on the extraction method, since the milling rate differs
299 markedly in the methods known as traditional, two-phases, and three phases (Civantos,
300 1999b). When the height of the olive in the pile exceeds certain limits, the lower layers of
301 the product suffer squashing and even crushing. Then, this generates tissue damage, rupture
302 of the fruit’s pericarp and liquid leak, favouring the conditions for acting various
303 microorganisms (Gutiérrez, R., Dobarganes, M.C., Gutiérrez, F., & Olías, J.M., 1981). The
304 circumstances above bound to the presence of the fruit mechanical damage during harvest,
305 formerly performed mostly by shaking the olive trees with chestnut rods, a method
306 increasingly fewer used. The main causes of mechanical damage include unsuitable harvest
307 methods, damage in transport, damage due to singularities in the travel from the receiving
308 hopper to the olive mill, and olive height excess in the piles. However, the compounds
309 produced by microorganisms are not only volatiles, nor only present in the olive piles.
310 Major cause of microbial spoilage, with fruit’s mechanical damage, is the degree of
311 cleaning and the presence of moisture. Contamination with ground or mud is frequent
312 (Alba, 2013). Also olives are normally wet, since the harvest time coincides with the fall, a
313 rainy season in Europe. Therefore, microbes growth in each batch of olives will largely
314 depend on its conditions specific on the above factors.
315 Besides the microbiological contamination after harvesting as well the mechanical damage
316 suffered by the olives before milling, one must see the whole line of olive oil production.
317 After grinding, the master miller, cares on preserving the cleanliness of the different
318 mechanical in contact with the olive paste or the olive oil.
319 One wonders to what extent upgrading the entire production, which is a proven fact from
320 the olive tree flowering to olive oil packaging, has led to improvement of the quality of
321 olive oil. According to data from the Statistical Yearbook (Ministry of Agriculture, 1980-
322 2000) shown in Table 1, the percentage of EVOO from 1980-2000 was relatively stable
323 around 55% of the total. In the middle of the last decade this figure was somehow lower.
324 There are several possible considerations about standards changes, which affect the olive
325 oil quality in the statistics. However, it is objective to say there is a long way to avoid the
326 generation of sensory defects in olive oils within the production itself. We believe that
327 progress in this direction should continue.
329 It is well known that olive oil free of foreign substances is resistant to microbial spoilage,
330 since it contains polyphenolic compounds with high antimicrobial activity (Cicerale, Lucas
331 & Keast, 2012). Microbial growth is favoured by the presence of other substances in olive
332 oil. These are mainly solid fruit rests and watery fraction, as well any possible
333 contamination from soil that has been able to pass after fruit washing before milling. Then,
334 the chemical changes provide substrate for the microorganism development. These
335 conditions can occur in the following critical points.
337 In the olive mill itself, even after cleaning, traces of moisture, mesocarp, endocarp and
338 seeds may remain. Although the volume inside this is small, this fact may be more common
339 than people thinks, when the cleaning is weak. This waste material affects the next olive
340 batch. An ‘old’ olive paste fraction altered by microorganisms will join the fresh product,
341 with the consequent risk of defect in the final virgin olive oil (Alba, 2013). Characterising
342 the microorganisms that act at this point and the specific changes they can induce, remains
343 unknown to the best of our knowledge.
345 When the olive paste contains an inoculum microbial, the paste beating is providing the
346 conditions for microbes growth and the related disturbances. Usually the beating
347 temperature recommended is below 30 °C, although depending on the characteristics of the
348 dough this feature can be at higher limits (Civantos, 1999a). Sometimes an excessive
349 temperature of the olive paste beating leads directly to the defect known as burnt or heated,
350 as already mentioned. An olive mass at 30 °C carrying a specific microbial inoculum can
351 remember to wheat flour’s dough voluntarily inoculated with yeast, which kneads in the
352 bread machine. In this case, after 30 minutes fermentation time, the yeast grows and is
353 perceptible. One may think that something similar can happen at a different scale in some
354 fractions of the olive paste. A large gap exists between these two cases, especially for the
355 important capacity of the olive phenolic compounds to inhibit large number of microbial
356 species (Soler-Rivas, Espin & Wichers, 2000). The inoculum necessary can easily come
357 from the mill machine because of the difficulty in cleaning the small areas in the beater.
358 This possible microbial when beating the olive paste remains not described and not
359 quantified, but it is reasonable to think it happens.
361 In this case we will focus on the two-phase system, used mainly. Once completed the
362 beaten of olive paste, a pump pushes it into the centrifugation machinery. The centrifuge
363 must be susceptible of a proper cleaning. However, it is not inconceivable there might be
364 pipe's singularities, difficult to cleaning and potential hot spots prone to microbial growth.
365 After separation of the olive oil from the solid debris and the watery phase within the
366 decanter, the produce passes a series of sieves. Each of these mechanics, the decanter in
367 particular, is susceptible to cleaning defects (Alba, 2013). Worthy is to consider possibility
368 of new machinery designs for an easier cleaning, which could provide valuable
369 improvement. Therefore, foam's appearance in a quantity that depends on the cleanliness is
370 not uncommon, providing a substratum susceptible to alcoholic fermentation. In these
371 circumstances, alcoholic fermentations can produce certain quantities of ethanol or
372 methanol. Thereby providing the necessary substrates to form alkyl esters and for
373 incorporating sensory defects to olive oil (Gómez-Coca, Moreda, & Pérez-Camino, 2012).
374 As in the precedent mechanic spots, the description and characterisation of the
375 microorganisms acting at these points, and its specific relation with the different olive oil
376 sensory defects remains unreported.
377 Tanks
378 Ideally, the tanks used for olive oil storage from different classes should be free of any
379 material other than olive oil. This means the tanks must be free of contamination from any
380 water fraction or any other matter. However, the olive oil normally has some moisture.
381 Moreover it is usual the condensation of water from the air contained in the tank, due to
382 lowering the environmental temperature, which results in the existence of a watery fraction.
383 This is the ingredient necessary for lipid hydrolysis and free fatty acid (FFA) generation by
384 chemical or enzymatic actions (Alba et al., 1996). These FFA released can crumble into
385 shorter chain fatty acids, causing bad odours and flavours (Civantos, 1999a). This is the
386 reason it is advisable to replace the air in the empty part of olive oil deposits with nitrogen
387 (Leone, Romaniello, & Tamborrino, 2013).
389 The olive pomace and the olive cake has been the subject of intense microbiological
390 research (Maestro, Borja, Martín, Fiestas & Alba, 1991; Borja, Martín, Alonso, García &
391 Banks, 1995; Millán et al., 2000; Borja, Rincon & Raposo, 2006, among many others), thus
392 the existing knowledge is extensive. By contrast, microbiological research within olive oil
393 elaboration, including post-harvest life of olives, is little.
394 Describing the microorganisms involved in inducing olive oil sensory defects within the
395 olive mill, can be useful. Especially about their taxonomic diversity, their specific growth
396 conditions and the sensory defect related. Identifying species affecting each substrate and
397 defining its biology and its final products may be important, as well as the possible specific
398 relation microorganism-defect. It is desirable to increase the awareness on the need of
399 protocols from the perspective of the microbiological hygiene. Ensuring the cleanliness of
400 each mechanic unit in the extraction would allow improving the quality of the olive oil.
401 Can assume that most micro-flora in the mechanic units of the olive mill come from the
402 olive tree. There may be another part from the agro-ecosystem in which the industry is
403 established, soil microorganisms mainly. Olive paste is a medium in which a high number
404 of fungal species is present. An example of this is a recent study in which fifty-three fungi
405 strains were isolated in olive products (Alves, Romo-Sánchez, Úbeda-Iranzo & Briones-
406 Pérez, 2012). The authors found ten different species in the olive paste, followed by the
407 olive fruit and the olive pomace, with five species each. Among all those species, six were
408 typically of olive paste (Penicillium chrysogenum, Rhizopus oryzae, Lichtheimia
409 corymbifera, Penicillium crustosum, Mucor circinelloides and Aspergillus niger), whereas
410 Mucor fragilis was found only in fresh olives and Rhizomucor variabilis var. regularior
411 only in olive pomace. The main objective of such a study was identifying enzymes with
412 potential biotechnological utility, thus no mention olive oil quality.
413 Olives are probably the main vehicle arrival of microbial population to the mill. Yeasts are
414 especially abundant in the olives, with Pseudomonads, lactic acid bacteria and
415 Enterobacteriaceae in a lower account, according to data reported by Tassou, Panagou &
416 Nychas (2010). As well, the microflora of olive fruits of the Greek variety ‘Amfissis’ were
417 studied (Fakas et al., 2010), and a wide number of microbial species reported, as Fusarium
418 spp, Penicillium spp, Aspergillus sp. Rhizopus nigricans, Paecilomyces sp. and Verticillium
419 sp., as well yeasts belonging to the genera of Candida, Cryptococcus, Pichia, Rhodotorula,
420 Debaryomyces, Saccharomycodes and Wickerhamiella. Gram positive bacilli and cocci
421 were also identified, as that from the genera Actinomyces, Corynebacterium, Listeria,
422 Pseudomonas and Vibrio, although only their lipase and lipoxygenase activities were
423 investigated. We must highlight that these data agrees with the importance of ethanol and
424 methanol in muddy, mouldy, fusty and vinegary flavours, before referred (Table 2). It is
425 logical to think there are differences in the microbial population from the olives surface
426 among different geographical origins and varieties. Could be this fact related to some of the
427 sensory characteristics of virgin olive oils?
428 Olive oil contains solid particles and micro-drops of vegetation water which settle during
429 the produce’s storage. Noteworthy is the unfiltered virgin olive oil is found in the market.
430 In fact, avoiding olive oil filtration is reported as desirable for extending olive oil’s shelf
431 life (Frega, Mozzona, & Lercker, 1999). The reason given is the dispersed particles play a
432 double stabilising effect on both oxidative and hydrolytic degradation. However, suspended
433 matter in the olive oil or that deposited on the bottom of the tanks could contribute to
434 fermentation, since the lack of filtering allows moisture to remains in the olive oil, thereby
435 the microbial content can be higher. In fact, Ciafardini & Zullo (2002a) reported that
436 together the suspended material in the olive oil, there are a rich microflora mainly
437 composed of yeasts. Besides, the same authors shown the partial elimination of the
438 sediments in extra virgin olive oil, carried out with cotton filtration by the bottling
439 companies, allows a significant decrease of the number of micro-organisms.
440 Certain microbial species communicate certain desirable attributes to many foods such as
441 dairy and meat products, bread, wine and other drinks, as well table olives. The question is,
442 could certain virgin olive oils obtain some benefits from microorganisms the way other
443 products do? This sets up a captivating field of research, and there are already some
444 evidences. Some of the virgin olive oil yeast microflora is useful, as they improve the
445 organoleptic characteristics of the olive oil during preservation (Zullo, Cioccia, &
446 Ciafardini, 2010). The same authors point out that other yeasts are harmful, as they can
447 damage the quality of the olive oil through the triglycerides hydrolysis. Yeasts in stored
448 olive oil have been studied (Ciafardini & Zullo, 2002b), showing that oleuropein present in
449 olive oil can be hydrolysed by β-glucosidase from the yeasts Saccharomyces cerevisiae and
450 Candida wickerhamii. The authors also noted the absence of lipases in the mentioned
451 yeasts, suggesting their positive contribution to olive oil sensory quality, without altering
452 the triglycerides composition. In the other hand, the influence during olive oil storage on its
453 sensory characteristics of some yeast strains belonging to Candida spp have been recently
454 reported (Zullo, Cioccia, & Ciafardini, 2013). The authors above have shown that all the
455 tested yeasts, used to inoculate EVOO, survived more than four months of storage. In the
456 same work muddy-sediment, rancid or both defects were found in olive oil samples treated
457 with C. adriatica, C. wickerhamii and C. diddensiae specific strains. In the same study,
458 olive oil samples treated with C. diddensiae strains were defect-free after four months of
459 storage, and still categorized as extra virgin.
460 Therefore it seems obvious that a deeper understanding of the microbiological events which
461 happen in the different steps of the olive oil mills, will be welcome. This would contribute
462 to clarify the influence of microorganisms in shaping the enormous diversity of sensory
463 'fingerprints' of the virgin olive oils.
464 References
465 Alba, J., Hidalgo, F., Ruíz, M. A., Martínez, F., Moyano, M. J., Cert, A., Pérez-Camino, M.
466 C. & Ruíz, M. V. (1996). Características de los aceites de oliva de primera y segunda
467 centrifugación. Grasas y Aceites, 47, 163-181.
468 Alba, J. (2013). Forecasts of the 2013 campaign. II Foss Meeting with the Olive Sector.
469 Instituto de la Grasa, CSIC, Sevilla. September, 19.
470 Alves, M., Romo-Sánchez, S., Úbeda-Iranzo, J., & Briones-Pérez, A. I. (2012). Fungi
471 isolated from olive ecosystems and screening of their potential biotechnological use. New
472 Biotechnology, 29, 451-456.
473 Andrewes, P., Busch, J. L. H. C., De Joode, T., Groenewegen, A., & Alexandre, H. (2003).
474 Sensory properties of virgin olive oil polyphenols: Identification of deacetoxyligstroside
475 aglycon as a key contributor to pungency. Journal of Agricultural and Food Chemistry, 51,
476 1415–1420.
477 Angerosa, F., Lanza, B., & Marsilio, V. (1996). Biogenesis of ‘fusty’ defect in virgin olive
478 oils. Grasas y Aceites, 47, 142–150.
479 Angerosa, F., Lanza, B., D'Alessandro, N., Marsilio, V., & Cumitini, S. (1999). Olive oil
480 off-odour compounds produced by Aspergillus and Penicillium. Acta Horticulturae, 474,
481 695-699.
482 Angerosa, F. (2000). Sensory quality of olive oils. In J. Harwood & R. Aparicio (Eds.),
483 Handbook of olive oil: Analysis and properties (pp. 355-392). Gaithersburg: Aspen
484 publications Inc.
485 Angerosa, F. (2002). Influence of volatile compounds on virgin olive oil quality evaluated
486 by analytical approaches and sensory panels. European Journal of Lipid Science and
487 Technology, 104, 639–660.
488 Angerosa, F., Servili, M., Selvaggini, R., Taticchi, A., Esposto, S., & Montedoro, G. F.
489 (2004). Volatile compounds in virgin olive oil: occurrence and their relationship with the
490 quality. Journal of Chromatography A, 1054, 17–31.
491 Aparicio, R., & Morales, M. T. (1998). Characterization of olives ripeness by green aroma
492 compounds of virgin olive oil. Journal of Agricultural and Food Chemistry, 46, 1116–
493 1122.
494 Aparicio, R., Morales, M. T., & García-González, D. L. (2012). Towards new analyses of
495 aroma and volatiles to understand sensory perception of olive oil. European Journal of
496 Lipid Science and Technology, 114, 1114-1125.
497 Borja, R., Martín, A., Alonso, V., García, I, & Banks, C. J. (1995). Influence of different
498 aerobic pretreatments on the kinetics of anaerobic digestion of olive mill wastewater. Water
499 Research, 29, 489–495.
500 Borja, R., Rincon, B., & Raposo, F. (2006). Anaerobic biodegradation of two-phase olive
501 mill solid wastes and liquid effluents: kinetic studies and process performance. Journal of
502 Chemical Technology and Biotechnology, 81, 1450-1462.
503 Buettner, A., & Schieberle, P. (2000). Influence of mastication on the concentration of
504 aroma volatiles. Some aspects of flavour release and flavour perception. Food Chemistry,
505 71, 347–354.
506 Caponio, F., Gomes, T., & Pasqualone, A. (2001). Phenolic compounds in virgin olive
507 oils: influence of the degree of olive ripeness on organoleptic characteristics and shelf-life.
508 European Food Research and Technology, 212, 329–333.
509 Cayuela, J. A., Peña, F., & García, J. A. (2013). Classification of olive oil and prediction of
510 the intensity of their sensory attributes using NIR and VIS/NIR spectroscopy. XVI
511 Simposium Científico-Técnico Expoliva. May 08-10, Jaén.
512 Ciafardini, G., & Zullo, B. A. (2002a). Survival of micro-organisms in extra virgin olive oil
513 during storage. Food Microbiology, 19, 105-109.
514 Ciafardini, G., & Zullo, B. A. (2002b). Microbiological activity in stored olive oil.
515 International Journal of Food Microbiology, 75, 111–118.
516 Cicerale, S., Lucas, L. J., & Keast, R. S. J. (2012). Antimicrobial, antioxidant and anti-
517 inflammatory phenolic activities in extra virgin olive oil. Current Opinion in
518 Biotechnology, 23, 129-135.
519 Civantos, L. (1999a). Obtención del aceite de oliva virgen. (2nd ed.). Madrid: Editorial
520 Agrícola Española, S.A., (Chapter 2).
521 Civantos, L. (1999b). Obtención del aceite de oliva virgen. (2nd ed.). Madrid: Editorial
522 Agrícola Española, S.A., (Chapter 8).
523 Del Barrio A., Gutiérrez, F, & Gutiérrez, R. (1981). Aplicación de la cromatografia gas-
524 líquido, técnica de espacio de cabeza, al problema del atrojado de los aceites de oliva. I.
525 Grasas y Aceites, 32,155–161.
526 European Comission (1991). Commission Regulation EEC Nr. 2568/91 of the Comission
527 on the characteristics of olive oils and olive pomace oils and their analytical methods.
528 Official Journal of the European Community, L248, 1-83.
537 Fakas, S., Kefalogianni, I., Makri, A., Tsoumpeli, G., Rouni, G., Gardeli, C., Papanikolaou,
538 S., & Aggelis, G. (2010). Characterization of olive fruit microflora and its effect on olive
539 oil volatile compounds biogenesis. European Journal of Lipid Science and Technology,
540 112, 1024-1032.
541 Frega, N., Mozzona, M., & Lercker, G. (1999). Effects of Free Fatty Acids on Oxidative
542 Stability of Vegetable Oil. Journal of the American Oil Chemists Society, 76, 325-329.
543 Gómez-Coca, R. B; Moreda, W., & Pérez-Camino, M. (2012). Fatty acid alkyl esters
544 presence in olive oil vs. organoleptic assessment. Food Chemistry, 135, 1205–1209.
545 Gutiérrez, R., Dobarganes, M. C., Gutiérrez, F., & Olías, J. M. (1981). Componentes
546 volátiles en el aroma del aceite de oliva virgen. V. Aceites obtenidos de frutos atrojados.
547 Grasas y Aceites, 32, 299-303.
548 Iaria, D. L., Bruno, L., Macchione, B., Tagarelli, A., Sindona, G., Giannino, D., Bitonti, M.
549 B., & Chiappetta, A. (2012). The aroma biogenesis-related Olea europaea alcohol
550 dehydrogenase gene is developmentally regulated in the fruits of two O. europaea L.
551 cultivars. Food Research International, 49, 720-727.
552 International Olive Council (2009). Trade standard applying to olive oils and pomace oils.
553 T.15/NC Nr 3/Rev. 4, 1-19.
554 International Olive Council (2010). Trade standard applying to olive oils and olive pomace
555 oils. COI/T. 15/NC No 3/Rev. 5, 1-19.
556 International Olive Council (2013a). Method for the organoleptic assessment of virgin olive
557 oil. T.20/Doc. No 15/Rev. 6, 1-18.
558 International Olive Council (2013b). Trade standard applying to olive oils and olive-
559 pomace oils. COI/T. 15/Doc. No 3/Rev. 7, 1-19.
560 International Olive Council (2015). World olive oil figures. UE olive oil figures.
561 http://www.internationaloliveoil.org/estaticos. Accessed January 2015.
562 Kalua, C. M., Allen, M. S., Bedgood, D. R., Bishop, A. G, Prenzler, P. D., & Robards, K.
563 (2007). Olive oil volatile compounds, flavour development and quality: A critical review.
564 Food Chem. 100, 273–286.
565 Leone, A., Romaniello, R., & Tamborrino, A. (2013). Development of a prototype for
566 extra-virgin olive oil storage with online control of injected nitrogen. Transactions of the
567 ASABE, 56, 107-1024.
568 Lerma-García, M. J., Cerretani, L., Cevoli, C., Simó-Alfonso, E. F., Bendini, A., & Toschi,
569 T.G. (2010). Use of electronic nose to determine defect percentage in oils. Comparison
570 with sensory panel results. Sensors and Actuators, B: Chemical 147, 283-289.
571 Luaces, P., Pérez, A. G., & Sanz, C. (2003). Role of olive seed in the biogenesis of virgin
572 olive oil aroma. Journal of Agricultural and Food Chemistry, 51, 4741-4745.
573 Luna, G., Morales, M. T., & Aparicio, R. (2006). Characterisation of 39 varietal virgin
574 olive oils by their volatile composition. Food Chemistry, 98, 243–252.
575 Maestro, R., Borja, R., Martín, A., Fiestas, J. A., & Alba, J. (1991). Biodegradación de los
576 compuestos fenólicos presentes en el alpechín. Grasas y Aceites, 4, 271–276.
577 Millán, B., Lucas, R., Robles, A., García, T., Alvarez de Cienfuegos, G., & Gálvez, A.
578 (2000). A study on the microbiotica from olive-mill wastewater (OMW) disposal lagoons,
579 with emphasis on filamentous fungi and their biodegradative potential. Microbiological
580 Research, 155, 143–147.
581 Ministry of Agriculture, Government of Spain. Olive. In Statistical Yearbook, years 1980-
582 2009 (Chapter 14). Accessed March 2013.
583 http://www.magrama.gob.es/es/estadistica/temas/publicaciones/anuario-de-estadistica
584 Morales, M. T., Aparicio, R., & Rios, J. J. (1994). Dynamic head space gas
585 chromatographic method for determining volatiles in virgin olive oil. Journal of
586 Chromatography A, 668, 455–462.
587 Morales, M. T., Luna, G., & Aparicio, R. (2005). Comparative study of virgin olive oil
588 sensory defects. Food Chemistry, 91, 293–301.
589 Nagata, Y., & Takeuchi, N. (1990). Measurement of odor threshold by triangle odor bag
590 method. Bulletin of Japan Environmental Sanitation Center, 17, 77–89.
591 Olías, J. M., Del Barrio A., & Gutiérrez. R. (1977). Componentes volátiles en el aroma del
592 aceite de oliva virgen. Grasas y Aceites, 28, 107-113.
593 Olías, J. M., Pérez, A. G., Ríos, J. J., & Sanz, L. C. (1993). Aroma of virgin olive oil:
594 biogenesis of the ‘green’ odour notes. Journal of Agricultural and Food Chemistry, 41,
595 2368-2373.
596 Pérez-Camino, M. C., Moreda, W., Mateos, R., & Cert, A. (2002). Determination of esters
597 of fatty acids with low molecular weight alcohols in olive oils. Journal of Agricultural and
598 Food Chemistry, 50, 4721–4725.
599 Procida, G., Giomo, A., Cichelli, A., & Conte, L. S. (2005). Study of volatile compounds of
600 defective virgin olive oils and sensory evaluation: a chemometric approach. Journal of
601 Science of Food and Agriculture, 85, 2175–2183.
602 Purcaro, G., Cordero, C., Liberto, E., Bicchi, C., & Conte, L. S. (2014). Toward a definition
603 of blueprint of virgin olive oil by comprehensive two-dimensional gas chromatography.
604 Journal of Chromatography A, 1334, 101–111.
605 Reboredo, P., González, C., Cancho, B., & Simal, J. (2013). Aroma biogenesis and
606 distribution between olive pulps and seeds with identification of aroma trends among
607 cultivars. Food Chemistry, 141, 637-643.
608 Reiners, J., & Grosch, W. (1998). Odorants of Virgin Olive Oils with Different Flavor
609 Profiles. J. Agric. Food Chem., 46, 2754-2763.
610 Ridolfi, M., Terenziani, S., Patumi, M., & Fontanazza, G. (2002). Characterization of the
611 lipoxygenases in some olive cultivars and determination of their role in volatile compounds
612 formation. Journal of Agricultural and Food Chemistry, 50, 835-839.
613 Rosenthal, A., Pyle, D. L., & Niranjan, K. (1996). Aqueous and enzymatic processes for
614 edible oil extraction. Enzyme and Microbial Technology, 19, 402–420.
615 Rothe, M., & Thomas, B. (1963). Aromastoffe des Brotes. Versuch einer Auswertung
616 chemnischer Gerschmacksanalysen mit Hilfe des Schwellenwertes. Zeitchrift fuer
617 Lebensmitte luntersuchung und Forschung, 119, 302–310.
618 Salas, J. J., & Sanchez, J. (1998). Alcohol dehydrogenases from olive (Olea europaea)
619 fruit. Phytochemistry, 48, 35-40.
620 Salas, J. J., & Sánchez, J. (1999). The decrease of virgin olive oil flavor produced by high
621 malaxation temperature is due to inactivation of hydroperoxide lyase. Rapid
622 Communication. Journal of Agricultural and Food Chemistry, 47, 809-812.
623 Salas, J. J., Williams, M., Harwood, J. L., & Sanchez, J. (1999). Lipoxygenase activity in
624 olive (Olea europaea) fruit. Journal of the American Oil Chemists Society, 76, 1163-1168.
625 Salas, J. J. (2004). Characterization of alcohol acyltransferase from olive fruit. Journal of.
626 Agricultural and Food Chemistry 52, 3155-3158.
627 Salas, J., Harwood, J., & Martínez, E. (2013). Lipid metabolism in olive: Biosynthesis of
628 triacylglycerols and aroma components. In R. Aparicio, & J. Harwood (Eds.), Handbook of
629 olive oil: Analysis and properties (pp. 97-127). New York: Springer Science+Business
630 Media.
631 Sánchez-Ortiz, A., Pérez, A. G., & Sanz, C. (2007). Cultivar differences on nonesterified
632 polyunsaturated fatty acid as a limiting factor for the biogenesis of virgin olive oil aroma.
633 Journal of Agricultural and Food Chemistry, 55, 7869-7873.
634 Sánchez-Ortiz, A., Pérez, A. G., Sanz, C. (2013). Synthesis of aroma compounds of virgin
635 olive oil: Significance of the cleavage of polyunsaturated fatty acid hydroperoxides during
636 the oil extraction process. Food Research International, 54, 1972-1978.
640 Sinelli, N., Cerretani, L., Egidio, V. D., Bendini, A., & Casiraghi, E. (2010). Application of
641 near (NIR) infrared and mid (MIR) infrared spectroscopy as a rapid tool to classify extra
642 virgin olive oil on the basis of fruity attribute intensity. Food Research International, 43,
643 369-375.
644 Soler-Rivas, C., Espin, J. C., & Wichers, H. J. (2000). Oleuropein and related compounds.
645 Journal of the Science of Food and Agriculture, 7, 1013-1023.
646 Tassou, C. C., Panagou, E. Z., & Nychas, J. E. (2010). Microbial colonization of naturally
647 fermented olives. In V. R. Preedy & R. R. Watson (Eds.), Olives and olive oil in healh and
648 disease prevention (pp. 397-406). Amsterdam: Elsevier Academic Press.
649 Tena, N., Lazzez, A., Aparicio, R., & García, D. L. (2007). Volatile compounds
650 characterizing tunisian Chemlali and Chétoui virgin olive oils. J. Agric. Food Chem., 55,
651 7852–7858.
652 Velasco, J.; & Dobarganes, C. (2002). Oxidative stability of virgin olive oil. European
653 Journal of Lipid Science Technology, 104, 661–676.
654 Zullo, B. A., Cioccia, G., & Ciafardini, G. (2010). Distribution of dimorphic yeast species
655 in commercial extra virgin olive oil. Food Microbiology, 27, 1035-1042.
656 Zullo, B. A., Cioccia, G., & Ciafardini, G. (2013). Effects of some oil-born yeasts on the
657 sensory characteristics of Italian virgin olive oil during its storage. Food Microbiology, 36,
658 70-78.
659
Season EVOO VOO LOO VOO+LOO Tota
% % % %
1980-1985 254,522.33 55.0 191,679.83 41.0 16,284.33 4.0 207,964.17 45.0 462,48
1986-1990 295,103.20 52.4 230,416.00 41.0 37,832.20 7.0 268,248.20 47.6 563,35
1991-1995 310,501.80 58.8 201,188.00 38.0 16,117.80 3.0 217,305.80 41.2 527,80
1996-2000 456,242.00 52.9 345,280.25 40.0 61,482.50 7.0 406,762.75 47.1 863,00
2001-2005 562,518.60 50.3 419,702.80 38.0 136,287.40 12.0 555,990.20 49.7 1118,50
2006-2009 503,936.25 45.4 398,986.50 36.0 207,646.50 19.0 606,633.00 54.6 1110,56
Average 52.5 39.0 8.5 47.5
Table 1. Virgin olive oil production in Spain (t). EVOO, Extra Virgin Olive Oil; VOO, Virgin Olive
Lampante Olive Oil. All the figures express in yearly averages. (Own data from: Ministry of Agricul
Government of Spain. Olive. In Statistical Yearbook, years 1980-2009 (Chapter 14). Accessed March
http://www.magrama.gob.es/es/estadistica/temas/publicaciones/anuario-de-estadistica
660
Compound OT Muddy Mould Fusty Vinegary