<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">NR</journal-id><journal-title-group><journal-title>Natural Resources</journal-title></journal-title-group><issn pub-type="epub">2158-706X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/nr.2016.73013</article-id><article-id pub-id-type="publisher-id">NR-64777</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Earth&amp;Environmental Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Nutritional Composition of Sea Cucumber &lt;i&gt;Isostichopus&lt;/i&gt; sp.
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>ensy</surname><given-names>Vergara</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Adriana</surname><given-names>Rodr&amp;iacute;guez</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Grupo de Investigaci&amp;amp;oacute;n y Desarrollo Tecnol&amp;amp;oacute;gico en Acuicultura, Facultad de Ingenier&amp;amp;iacute;as, Universidad del Magdalena, Santa Marta, Colombia</addr-line></aff><pub-date pub-type="epub"><day>11</day><month>03</month><year>2016</year></pub-date><volume>07</volume><issue>03</issue><fpage>130</fpage><lpage>137</lpage><history><date date-type="received"><day>16</day>	<month>January</month>	<year>2016</year></date><date date-type="rev-recd"><day>accepted</day>	<month>18</month>	<year>March</year>	</date><date date-type="accepted"><day>21</day>	<month>March</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The knowledge of the chemical composition of invertebrates as sea cucumber contributes to improving our understanding of these living organisms. This study compared the chemical composition of wild sea cucumber 
  <em>Isostichopus</em> sp., between February 2013 and January 2014. Sea cucumbers were captured by hand by artisanal fishermen and transported alive to the laboratory of Aquaculture of the Universidad del Magdalena (Colombia), where they were subsequently killed and taken to freeze until analysis. For proximate analysis 20 g of muscle were used for each sample. The analysis (in triplicate) was performed according to [1]. Significant differences (p &lt; 0.05) in the protein content, lipids and ash were found. The chemical composition ranged from 2.74% to 6.63% for protein; about 0.07% to 0.35% for lipids; 3.16% to 3.81% for ash; between 83.74% and 86.92% for moisture. Chemical composition of muscle 
  <em>Isostichopus</em> sp. was similar to that reported for fresh sea cucumbers internationally traded, which indicates that it is a species with a competitive commercial value for use in food.
 
</p></abstract><kwd-group><kwd>Caribbean Sea</kwd><kwd> Chemical Composition</kwd><kwd> Isostichopus</kwd><kwd> Protein</kwd><kwd> Lipids</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Water, inorganic matter and a variety of organic compounds are part of the chemical composition of aquatic organisms [<xref ref-type="bibr" rid="scirp.64777-ref2">2</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref5">5</xref>] . This composition might be influenced by many factors such as physiological characteristics, habitat and life cycle of organisms, or by the environmental characteristics in where they live [<xref ref-type="bibr" rid="scirp.64777-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref7">7</xref>] .</p><p>Proteins, lipids and minerals are the main constituents of living organisms and knowledge about their concentration provides information related to the physiological and nutritional value of organisms [<xref ref-type="bibr" rid="scirp.64777-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref5">5</xref>] .</p><p>In living organisms, proteins play an important role in most biological processes, such as transportation, storage, immune protection and the generation and transmission of nerve impulses [<xref ref-type="bibr" rid="scirp.64777-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref8">8</xref>] . Lipids are hydrophobic substances that serve as energy reserves, contribute to the waterline and are structural components of cell membranes and organelles [<xref ref-type="bibr" rid="scirp.64777-ref9">9</xref>] . Minerals are involved in various biological functions with great importance as the formation of skeletal structures in the osmotic processes and muscle contraction [<xref ref-type="bibr" rid="scirp.64777-ref10">10</xref>] .</p><p>At present there is little information on the chemical composition in many aquatic species. Chemical composition studies comprise mainly organisms with economic importance such as freshwater fish and marine fish, crustaceans and mollusks, leaving away organism like sea cucumbers [<xref ref-type="bibr" rid="scirp.64777-ref11">11</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref16">16</xref>] . Thus, the information about nutritional composition is subject currently only to organisms of economic importance.</p><p>Isostichopus is within genres that are commercially exploited. Their high value is due to its use as food and in traditional Asian medicine. Studies in sea cucumbers include gender distribution, taxonomy, biological activity, aquaculture and nutritional composition besides others [<xref ref-type="bibr" rid="scirp.64777-ref17">17</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref19">19</xref>] . Analysis on fresh proximal composition has shown that these marine invertebrates have a high nutritional value, which can vary depending on the species, feeding behavior and seasonal variations [<xref ref-type="bibr" rid="scirp.64777-ref20">20</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref23">23</xref>] .</p><p>From a nutritional standpoint, sea cucumbers are of great value because of its high protein content, its low fat percentage and vitamin content, among which highlights the vitamins A, B<sub>1</sub> (thiamine), B<sub>2</sub> (riboflavin ), B<sub>3</sub> (niacin) and minerals, especially calcium, magnesium, iron and zinc [<xref ref-type="bibr" rid="scirp.64777-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref25">25</xref>] .</p><p>In Colombia, there are few studies on sea cucumbers [<xref ref-type="bibr" rid="scirp.64777-ref26">26</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref31">31</xref>] . This group of invertebrates is not well known and only some artisanal fishermen occasionally consume them as food. Although Isostichopus is a genus with high ecological impact due to the fact that they remove and oxygenate the natural substrate in which they live, and it’s a genus with great commercial interest worldwide, and not yet known aspects related to its proximal composition. Therefore, the objective of this research was to study the proximate composition of fresh Isostichopus sp., from the natural environment. The information will be useful to have basic knowledge about the nutritional values (percentages of protein, lipid, ash and moisture in the muscle) and their variations over an annual period of native species of sea cucumber in the Colombian Caribbean.</p></sec><sec id="s2"><title>2. Material &amp; Methods</title><p>A total of sixty specimens of Isostichopus sp. were collected monthly for one year (February 2013 to January 2014). They were captured from the Bay of Rodadero, Santa Marta (11˚13'22.73&quot;N - 74˚13'32.59&quot;W) and transported alive in plastic containers filled with sea water at 28˚C and 37 Practical Salinity Units (UPS) to the Aquaculture laboratory at the University of Magdalena. Once there, they were killed by hypothermia, internal fluids were drained and body weight (232.39 &#177; 78.71 g) was recorded with a precision scale (Brand Ohauss). Animals were cut longitudinally from the ventral portion, whereupon the viscera and the muscle bands were extracted from the body wall.</p><sec id="s2_1"><title>2.1. Proximal Composition Analysis</title><p>To chemical analysis composition 20 g of fresh muscle were used. The samples were processed at the Laboratory of Food Science (Universidad del Magdalena). Determining analysis (in triplicate) was performed according to [<xref ref-type="bibr" rid="scirp.64777-ref1">1</xref>] . The content of crude protein (N &#215; 6.25) was determined by the Kjeldahl method [<xref ref-type="bibr" rid="scirp.64777-ref1">1</xref>] . In the process a digester system with neutralizing gases, integrated recirculation pump and distiller (UDK 132, Velp Scrubber<sup>&#174;</sup> SMS, Italy), titration with hydrochloric acid a digital burette (50 ml) was used (Brand was used &#174;, Germany). Total lipids were extracted with diethyl ether extraction in a Fosstech analyzer after HCl hydrolysis and evaluated gravimetrically in an analytical balance (Adventurer-OHAUS™, China) [<xref ref-type="bibr" rid="scirp.64777-ref1">1</xref>] . The inorganic content (ash weight) was obtained by incinerating the samples in a muffle furnace at 550˚C (Vulcan 3-550™, USA). Pure dry ashes were calculated from the difference between the dry weight and wet weight. Moisture were determined using a moisture extractor digital balance (Ohaus MB45™, USA), and values were expressed as percentages.</p><p>In Colombia, two climate period are identified: a rainy season, from April to October, when fresh and brackish waters from the Magdalena River and Ci&#233;naga Grande de Santa Marta mangrove-estuarine system, reach the shelf in the central region and a dry season, from November to March, in which Northeastern Trades Winds induce upwelling. For the Caribbean coast the maximum annual precipitation values do not exceed 2500 mm. The average temperature is below 27˚C [<xref ref-type="bibr" rid="scirp.64777-ref32">32</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref36">36</xref>] .</p></sec><sec id="s2_2"><title>2.2. Statistical Analysis</title><p>To know the effect of time (a period of twelve months) on the proximal composition of Isostichopus sp., a one way analysis of variance was applied, after verification of compliance with the assumptions of normality (Kolmogorov-Smirnov) and homoscedasticity (Levene’s test). Since the ANOVA yielded a significant result (p &lt; 0.05), the Multiple Tukey test, was also applied to determine statistically difference between months. For all these tests the statistical program Statgraphics Centurion vs. XVI (2010) was used.</p></sec></sec><sec id="s3"><title>3. Results</title><p>The chemical composition of Isostichopus sp. is presented in <xref ref-type="table" rid="table1">Table 1</xref>. The protein content varied significantly (p &lt; 0.05), and their values were in the range of 2.74% and 6.63%, with the highest percentage found in July, while that minors were recorded between February and May (2013) and between November (2013) to January (2014).</p><p>Significant variations in lipids and ash between the months sampled (p &lt; 0.05) (<xref ref-type="table" rid="table1">Table 1</xref>) were found. The lipid content ranged from 0.07% &#177; 0.10% to 0.35% &#177; 0.44%; lipid percentages presented a variation from February to May and from June to December, being May when the highest percentage of lipid was observed. On the other hand, the ash content showed variations between the sampled months in this way, the highest percentage (3.81% &#177; 0.11%) was observed in August, and the lowest percentage (3.16% &#177; 0.55%), was presented in April.</p><p>The moisture content presented fluctuations during the sampled months, however it was in July where it reached its maximum value (86.92% &#177; 1.54%), while in January the minimum percentage of water was detected (83.74% &#177; 1.07%). Nevertheless, the statistical analysis showed that significant differences did not exist between the months sampled (p &lt; 0.05).</p></sec><sec id="s4"><title>4. Discussion</title><p>Knowledge of the chemical composition of species with potential for food human consumption is of great importance for nutritional characterization, however this content, may be influenced by animals feeding, physiological characteristics, life cycle and habitat of the species, besides the environmental features [<xref ref-type="bibr" rid="scirp.64777-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref37">37</xref>] .</p><p>There are few studies related to proximal muscle composition of sea cucumbers worldwide. The results found in muscle composition of individuals of Isostichopus sp. are within the ranges reported for other species such as Stichopus japonicus, Apostichopus japonicus, Parastichopus californicus, Holothuria tremula, Holothuria scabra and Cucumaria frondosa [<xref ref-type="bibr" rid="scirp.64777-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref38">38</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref41">41</xref>] .</p><p>In this study the protein content for Isostichopus sp. was between 2.74% and 6.63%, being within the ranges</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Chemical composition of muscle of sea cucumber Isostichopus sp., in terms of percentage (g/100g) of crude protein, lipid, ash and moisture during the months of sampling and represent the mean of tree replicates &#177; Standard Deviation (Fresh samples, n = 60)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Month</th><th align="center" valign="middle" >% Protein</th><th align="center" valign="middle" >% Lipid</th><th align="center" valign="middle" >% Ash</th><th align="center" valign="middle" >% Moisture</th></tr></thead><tr><td align="center" valign="middle" >Feb-13</td><td align="center" valign="middle" >3.12 &#177; 0.72<sup>ab</sup></td><td align="center" valign="middle" >0.09 &#177; 0.05<sup>ab</sup></td><td align="center" valign="middle" >3.77 &#177; 0.35<sup>bc </sup></td><td align="center" valign="middle" >84.83 &#177; 1.20<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Mar-13</td><td align="center" valign="middle" >2.96 &#177; 0.81<sup>ab</sup></td><td align="center" valign="middle" >0.13 &#177; 0.15<sup>ab</sup></td><td align="center" valign="middle" >3.37 &#177; 0.12<sup>ab</sup></td><td align="center" valign="middle" >85.78 &#177; 2.02<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Apr-13</td><td align="center" valign="middle" >2.74 &#177; 0.79<sup>a</sup></td><td align="center" valign="middle" >0.07 &#177; 0.10<sup>a</sup></td><td align="center" valign="middle" >3.16 &#177; 0.55<sup>a</sup></td><td align="center" valign="middle" >86.56 &#177; 2.45<sup>a</sup></td></tr><tr><td align="center" valign="middle" >May-13</td><td align="center" valign="middle" >3.21 &#177; 0.67<sup>ab</sup></td><td align="center" valign="middle" >0.35 &#177; 0.44<sup>bc</sup></td><td align="center" valign="middle" >3.36 &#177; 0.16<sup>ab</sup></td><td align="center" valign="middle" >84.10 &#177; 2.10<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Jun-13</td><td align="center" valign="middle" >6.17 &#177; 1.30<sup>d</sup></td><td align="center" valign="middle" >0.08 &#177; 0.06<sup>a</sup></td><td align="center" valign="middle" >3.44 &#177; 0.34<sup>abc</sup></td><td align="center" valign="middle" >85.66 &#177; 1.64<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Jul-13</td><td align="center" valign="middle" >6.63 &#177; 0.59<sup>d</sup></td><td align="center" valign="middle" >0.16 &#177; 0.07<sup>ab</sup></td><td align="center" valign="middle" >3.26 &#177; 0.59<sup>a</sup></td><td align="center" valign="middle" >86.92 &#177; 1.54<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Aug-13</td><td align="center" valign="middle" >5.43 &#177; 0.77<sup>c</sup></td><td align="center" valign="middle" >0.24 &#177; 0.35<sup>ab</sup></td><td align="center" valign="middle" >3.81 &#177; 0.11<sup>c</sup></td><td align="center" valign="middle" >83.96 &#177; 1.52<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Sep-13</td><td align="center" valign="middle" >5.34 &#177; 0.71<sup>c</sup></td><td align="center" valign="middle" >0.10 &#177; 0.06<sup>ab</sup></td><td align="center" valign="middle" >3.45 &#177; 0.20<sup>abc</sup></td><td align="center" valign="middle" >85.11 &#177; 1.85<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Oct-13</td><td align="center" valign="middle" >4.64 &#177; 0.46<sup>c</sup></td><td align="center" valign="middle" >0.13 &#177; 0.09<sup>ab</sup></td><td align="center" valign="middle" >3.51 &#177; 0.13<sup>abc</sup></td><td align="center" valign="middle" >84.44 &#177; 1.34<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Nov-13</td><td align="center" valign="middle" >3.70 &#177; 0.93<sup>b</sup></td><td align="center" valign="middle" >0.14 &#177; 0.07<sup>ab</sup></td><td align="center" valign="middle" >3.57 &#177; 0.67<sup>abc</sup></td><td align="center" valign="middle" >86.44 &#177; 1.37<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Dec-13</td><td align="center" valign="middle" >3.34 &#177; 0.81<sup>ab</sup></td><td align="center" valign="middle" >0.07 &#177; 0.06<sup>a</sup></td><td align="center" valign="middle" >3.57 &#177; 0.13<sup>abc</sup></td><td align="center" valign="middle" >86.28 &#177; 2.01<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Jan-14</td><td align="center" valign="middle" >3.15 &#177; 0.78<sup>ab</sup></td><td align="center" valign="middle" >0.07 &#177; 0.05<sup>a</sup></td><td align="center" valign="middle" >3.22 &#177; 0.26<sup>a</sup></td><td align="center" valign="middle" >83.74 &#177; 1.07<sup>a</sup></td></tr></tbody></table></table-wrap><p>* <sup>abcd</sup>Values in the same column with the different superscripts are significantly different (p &lt; 0.05).</p><p>reported by [<xref ref-type="bibr" rid="scirp.64777-ref42">42</xref>] in Stichopus japonicus (3.31% and 6.78%) and [<xref ref-type="bibr" rid="scirp.64777-ref21">21</xref>] , to Parastichopus spp. (2.5% and 13.8%); in turn, they are in the average range reported by [<xref ref-type="bibr" rid="scirp.64777-ref43">43</xref>] for Apostichopus japonicus (1.13% and 3.99%), although in this case the inferior value of this is very lower compared to that found in the species in this study. Moreover, Isostichopus sp. records are below those obtained by [<xref ref-type="bibr" rid="scirp.64777-ref24">24</xref>] , for Thelenota pineapple (16.64%) and Acaudina molpadioides (12.94%), or are relatively lower when compared to those reported by [<xref ref-type="bibr" rid="scirp.64777-ref23">23</xref>] , in H. polii, H. tubulosa and H. mammata (7.88 and 8.829%).</p><p>According to [<xref ref-type="bibr" rid="scirp.64777-ref20">20</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref23">23</xref>] ), seasonal variations affect bromatological content of sea cucumbers. Throughout this study, the percentage of protein presented dramatically fluctuations with the highest values from June to October at its maximum increase in July. This case is contrary to what was reported by [<xref ref-type="bibr" rid="scirp.64777-ref42">42</xref>] who reported that Stichopus japonicus showed variations in the protein content from January to August, while [<xref ref-type="bibr" rid="scirp.64777-ref40">40</xref>] reported values of protein of 9.53% and 5.78% of H. scabra in the spring and summer, indicating that these fluctuations may be related to the physiological characteristics, seasonal variations, the life cycle of the species and the and the study region [<xref ref-type="bibr" rid="scirp.64777-ref5">5</xref>] .</p><p>Moreover, the period where the highest values of protein were found coincides with the breeding season of the species recorded by [<xref ref-type="bibr" rid="scirp.64777-ref30">30</xref>] . It is possible that increased protein content has an influence on the mobilization of nutrients during the breeding season and subsequent release of sea cucumbers. It is well known that good nutrition on organisms in general is critical to optimizing reproductive processes and normal development of embryos. An optimal level of nutrients will determine the success in the morphology of eggs and hatching rates. However studies related to nutritional composition, diet, breeding seasons and reproductive success in sea cucumbers, are scarce, so this would be a preliminary reference on what happens inside the native sea cucumbers of the region against the reproductive processes vs. the composition and nutritional requirements thereof. Then, deep future studies should address in this regard.</p><p>Moreover, total lipid content found in this study presented variations during all the sampled months: the lowest percentage was observed in April and the largest increase in May. Despite belonging to the same family, the fat content of Isostichopus sp. (0.07 than 0.35%,) was much lower than that reported by Tanikawa et al. [<xref ref-type="bibr" rid="scirp.64777-ref42">42</xref>] , for Stichopus japonicus (0.56% to 2.3%), by [<xref ref-type="bibr" rid="scirp.64777-ref44">44</xref>] to Apostichopus japonicus (0.28% to 0.33%) and the findings by [<xref ref-type="bibr" rid="scirp.64777-ref38">38</xref>] , to Parastichopus californicus (0.57% and 0.44%). While [<xref ref-type="bibr" rid="scirp.64777-ref24">24</xref>] , reported values below related in this study, with a percentage of 0.27% to 0.03% for Thelenota ananas and Acaudina molpadioides. Finally, the results recorded for Isostichopus sp. in this work contrast with those found by [<xref ref-type="bibr" rid="scirp.64777-ref23">23</xref>] to H. tubulosa, H. polii and H. mammata who report lipid content between 0.09%, 0.15% and 0.18% respectively.</p><p>According to what observed by [<xref ref-type="bibr" rid="scirp.64777-ref45">45</xref>] , “lipids are greater metabolic energy source in reproduction processes of fish, which can be mobilized from a tissue storage until oocytes developing food purchased directly or synthesized de novo in the ovarian follicle”. In sea cucumbers is little the knowledge in this regard. According [<xref ref-type="bibr" rid="scirp.64777-ref42">42</xref>] variations in the fat content may be related to gonadal growth. This study showed an increase in lipid values in May, when as [<xref ref-type="bibr" rid="scirp.64777-ref30">30</xref>] , found Isostichopus sp. show gonads in vitellogenic stage and previtellogenic oocytes stage. Thus, the lipid concentration is likely to affect the reproductive potential of the species, which previously mobilize its lipid reserves for reproduction and development of gamete. As mentioned by [<xref ref-type="bibr" rid="scirp.64777-ref46">46</xref>] and [<xref ref-type="bibr" rid="scirp.64777-ref47">47</xref>] , who report that holothurians may have wide variations in lipid concentrations (and polyunsaturated fatty acids), depending on the reproductive pattern and the type of development of each specie, biochemical composition being listed as a factor species specific. Future studies should address in this regard, in order to know the class of lipid and the role they have on the reproductive function of the species.</p><p>Many factors are linked with changes in chemical composition in living organism [<xref ref-type="bibr" rid="scirp.64777-ref16">16</xref>] . Environmental changes has been reported as one of a key factor which could influences proximal composition in marine invertebrates [<xref ref-type="bibr" rid="scirp.64777-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref48">48</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref50">50</xref>] . Furthermore sea cucumber physiology, seasonal variations in feeding behavior, feeding regimes and food supply from sea environment are factors which may help explained variations on nutritional or chemical composition [<xref ref-type="bibr" rid="scirp.64777-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref51">51</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref53">53</xref>] . In addition, as state [<xref ref-type="bibr" rid="scirp.64777-ref54">54</xref>] , sea cucumbers may have different chemical composition including those sampled from the same environmental conditions. In Colombia there are two climatic periods: dry season and rainy season [<xref ref-type="bibr" rid="scirp.64777-ref36">36</xref>] . In this sense, lower protein and lipid levels were found during the dry season and the highest percentages were registered in rainy season which is also consistent with lower water temperature (27˚C) in the dry season and with a higher water temperature (28˚C) in the rainy season. Authors as [<xref ref-type="bibr" rid="scirp.64777-ref55">55</xref>] argue that changes in the lipid content in the sea cucumber are linked to the season and habitat. Similar trends have been found by [<xref ref-type="bibr" rid="scirp.64777-ref56">56</xref>] and [<xref ref-type="bibr" rid="scirp.64777-ref50">50</xref>] .</p><p>Ash content ranged from 3.16% to 3.81%; these variations are above the values reported by [<xref ref-type="bibr" rid="scirp.64777-ref42">42</xref>] for S. japonicus and [<xref ref-type="bibr" rid="scirp.64777-ref24">24</xref>] to T. ananas and A. molpadioides. Native values of sea cucumbers are lower than those reported by Aydin et al. [<xref ref-type="bibr" rid="scirp.64777-ref23">23</xref>] , for H. polii, H. tubulosa and H. mammata with a range between 5.13% and 7.85%. Fluctuations found in this study may be due as [<xref ref-type="bibr" rid="scirp.64777-ref42">42</xref>] and [<xref ref-type="bibr" rid="scirp.64777-ref57">57</xref>] recorded for sea cucumbers, who reported that the mineral content can be linked to the high content of spicules have sea cucumbers in their body. It should be noted that the ash content in this work was obtained from muscle integument without any procedure to extract the spicules (decalcification), so it is believed that this might affected the percentages of ash obtained for Isostichopus sp.</p><p>In the other hand, marine invertebrates’ humidity may vary between 65% and 95% with exceptions in some taxa [<xref ref-type="bibr" rid="scirp.64777-ref58">58</xref>] - [<xref ref-type="bibr" rid="scirp.64777-ref60">60</xref>] . During this study the moisture content was between 83.74% and 86.92%, which values are within the ranges established previously by [<xref ref-type="bibr" rid="scirp.64777-ref21">21</xref>] for sea cucumber, and within those reported by [<xref ref-type="bibr" rid="scirp.64777-ref23">23</xref>] (81.24% to 85.24%), for three Holothuria species (H. tubulosa, H. polii and H. mammata) and [<xref ref-type="bibr" rid="scirp.64777-ref42">42</xref>] , (84, 89% and 91.30%) in Stichopus japonicus. Humidity values in this study are above those reported by [<xref ref-type="bibr" rid="scirp.64777-ref54">54</xref>] (67.82% and 69.45%), in two species of sea cucumber Persian Gulf: H. arenicola and H. parva. These were recorded below that reported by [<xref ref-type="bibr" rid="scirp.64777-ref21">21</xref>] and [<xref ref-type="bibr" rid="scirp.64777-ref38">38</xref>] , (88.8% and 90.1%), in Parastichopus californicus and those exposed by [<xref ref-type="bibr" rid="scirp.64777-ref41">41</xref>] in Cucumaria frondosa (87.4% and 90.1%). Moisture percentages found in this study may be linked to the time of year, environmental factors, geographical variations or feeding behavior [<xref ref-type="bibr" rid="scirp.64777-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.64777-ref40">40</xref>] .</p><p>The results obtained in this study are consistent with those made in other species of sea cucumber, which allows us to set up that sea cucumbers, native of Santa Marta Caribbean Sea (Colombia), have a chemical composition with valuable nutritional properties, which could be used for consumption and pharmaceutical applications.</p></sec><sec id="s5"><title>5. Conclusion</title><p>As a conclusion, the compositional analysis showed that Isostichopus sp. possesses valuable nutritional properties, including high percentage of protein (6.63%) and low percentage of lipids (0.35%). In addition, the highest values of protein and lipid content in muscle are related to the reproductive season which is probably linked to patterns of reproductive biology of the species. The nutritional composition of Isostichopus sp. fluctuates in line with environment changes, where in the dry season, values are low and in the rainy season these are higher. Native sea cucumber Isostichopus sp might be a potential candidate to be commercialized in worldwide markets with the highest consumption of b&#234;che de mer or trepang. Isostichopus sp. could be used for human consumption because of its high nutritional value.</p></sec><sec id="s6"><title>Acknowledgements</title><p>This work was supported by Colciencias Grant (No 1117-521-28356) and Vicerrector&#237;a de Investigaci&#243;n (Universidad del Magdalena), Santa Marta, Colombia. Authors would like to thank sea cucumbers fisherman Jorge Polo who helped collecting holothurians and to the Group of Research and Technology Development in Aquaculture.</p></sec><sec id="s7"><title>Cite this paper</title><p>Wensy Vergara,Adriana Rodr&#237;guez, (2016) Nutritional Composition of Sea Cucumber Isostichopus sp.. Natural Resources,07,130-137. doi: 10.4236/nr.2016.73013</p></sec><sec id="s8"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.64777-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">AOAC (1990) Association of Official Analytical Chemists, Official Methods of Analysis. 15th Edition, AOAC International, Arlington.</mixed-citation></ref><ref id="scirp.64777-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Graeve, M., Albers, C. and Kattner, G. 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