<?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">OJMS</journal-id><journal-title-group><journal-title>Open Journal of Marine Science</journal-title></journal-title-group><issn pub-type="epub">2161-7384</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojms.2022.123005</article-id><article-id pub-id-type="publisher-id">OJMS-118258</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>
 
 
  Comparative Taxonomical Studies on the Egyptian Red Sea Cephalopods (Cephalopoda: Mollusca)
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rafik</surname><given-names>Riad</given-names></name><xref ref-type="aff" rid="aff1"><sub>1</sub></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>National Institute of Oceanography and Fisheries, (NIOF), Cairo, Egypt</addr-line></aff><pub-date pub-type="epub"><day>29</day><month>06</month><year>2022</year></pub-date><volume>12</volume><issue>03</issue><fpage>61</fpage><lpage>82</lpage><history><date date-type="received"><day>7,</day>	<month>May</month>	<year>2022</year></date><date date-type="rev-recd"><day>27,</day>	<month>June</month>	<year>2022</year>	</date><date date-type="accepted"><day>30,</day>	<month>June</month>	<year>2022</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>
 
 
  Cephalopods are known to be commercially important around the world. Worth mentioning it constitutes a major part of the Egyptian fishing industry. Samples of cephalopods were collected from fishing boats in the Suez Gulf and Egyptian Red Sea. Cuttlefishes, squids, and octopuses had their club of the tentacle, arm IV hectocotylus, sucker of the club of the tentacle, sucker ring of the club of the tentacle, arm sucker, arm sucker ring, radula, gill, and shell. Various organs were photographed using a Canon G7X
   
  digital Camera. Eleven Egyptian Red Sea cephalopod species were encountered; three of them are cuttlefish species namely: Sepia dollfusi, Sepia pharaonis, and Sepia elongata. Three squid species namely: Loligo forbesii, Uroteuthis Photololigo duvaucelii, and Sepioteuthis lessoniana were also encountered. Five octopus species were also recorded namely: Octopus vulgaris, Callistoctopus macropus, Macrotritopus defilippi, Amphyoctopus aegina, and Amphyoctopus membranaceus. Aims of the current work are to differentiate between some Cephalopod species living in the Red Sea of Egypt and evaluate the status to achieve a reliable differentiation between these species.
  
 
</p></abstract><kwd-group><kwd>Comparative Cephalopods</kwd><kwd> Egyptian</kwd><kwd> Red Sea</kwd><kwd> Taxonomy</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Cephalopods (class Cephalopoda) are the phylum Mollusca’s most perplexing group of invertebrates. If not all are of the invertebrate phyla. It simply gathers marine animals found in all areas of the world save the Black Sea, from the Arctic to the Antarctic, and from surface waters to deep seas.</p><p>For cephalopods, salinity is a limiting factor in their circulation.</p><p>They are mostly limited to salinities in the range of 27. However, Lolliguncula brevis, which lives and imitates in water with a salinity of 17, has a better salt resistance (Hendrix et al. [<xref ref-type="bibr" rid="scirp.118258-ref1">1</xref>]).</p><p>The Red Sea and the southern banks of the Liberian Peninsula have a few different types of cephalopods (Riad and Gabr [<xref ref-type="bibr" rid="scirp.118258-ref2">2</xref>]) where salinity exceeds 37. The Sea of Marmara has a diverse diversity of species, with salinities ranging from 25 to 18 (Unsal et al. [<xref ref-type="bibr" rid="scirp.118258-ref3">3</xref>]).</p><p>Many investigations were conducted in the twentieth century. Robson [<xref ref-type="bibr" rid="scirp.118258-ref4">4</xref>] identified six cephalopod species and recorded three Cephalopod species from the Suez Canal. Adam [<xref ref-type="bibr" rid="scirp.118258-ref5">5</xref>] recorded ten Cephalopod species in the Suez Gulf and three in the Aqaba Gulf. Adam [<xref ref-type="bibr" rid="scirp.118258-ref6">6</xref>] recorded seven Cephalopod species from the Gulf of Aqaba.</p><p>Many investigations in the 20 and 21st century Emam [<xref ref-type="bibr" rid="scirp.118258-ref7">7</xref>] investigated Sepia prashadi and Sepia savignyi from the Gulfs of Suez and Aqaba in the Red Sea waters.</p><p>The male reproductive system of Sepioteuthis lessoniana from the Suez Gulf was investigated by Mangold [<xref ref-type="bibr" rid="scirp.118258-ref8">8</xref>].</p><p>Emam, et al. [<xref ref-type="bibr" rid="scirp.118258-ref9">9</xref>] studied morphology, morphometry, age, and growth of Loligo duvaucelii from the Suez Gulf. Riad &amp; Gabr [<xref ref-type="bibr" rid="scirp.118258-ref2">2</xref>] performed a comparative study on Octopus vulgaris from the Egyptian Mediterranean and Red Sea. Gabr and Riad [<xref ref-type="bibr" rid="scirp.118258-ref10">10</xref>] investigated the reproductive biology and morphometric characteristics of Loligo forbesii from Suez Gulf. Riad and Abd EL Hafez [<xref ref-type="bibr" rid="scirp.118258-ref11">11</xref>] conducted bioeconomic importance of the Egyptian Red Sea squid. Kilada and Riad [<xref ref-type="bibr" rid="scirp.118258-ref12">12</xref>] studied the seasonal biochemical composition of Loligo forbesii in the Egyptian Mediterranean and the Gulf of Suez, Red Sea. The population dynamics of Octopus defilippi caught from the Egyptian Red Sea was examined by Elganainy and Riad [<xref ref-type="bibr" rid="scirp.118258-ref13">13</xref>]. In the Egyptian Red Sea, Kilada and Riad [<xref ref-type="bibr" rid="scirp.118258-ref14">14</xref>] investigated the seasonal reproductive biology of Uroteuthis duvaucelii (Cephalopoda: Loliginidae).</p><p>Osman, et al. [<xref ref-type="bibr" rid="scirp.118258-ref15">15</xref>] investigated the feeding science and biochemical organization of Lessepsian Octopus Octopus aegina from the Egyptian Red Sea’s Suez Gulf.</p><p>The goal of this study is to learn more about the cephalopod species that live in the Egyptian Red Sea waters and to distinguish between them based on the little taxonomic information available (Roper, et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>], Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>], Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>] and Jereb, et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>]).</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>Seasonally, cephalopod samples were obtained from commercial fishing trawlers in the Suez Gulf and the Egyptian Red Sea (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>The samples were kept in seawater that contained 5% formalin. The following traits for cuttlefishes, squids, and octopuses were thoroughly analyzed to identify</p><p>specimens to the species level, according to Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>], Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>]), and Jereb, et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>] respectively. These are tentacular club sucker, tentacular club sucker ring, arm IV of hectocotylus, arm sucker, arm sucker ring, radula, gill, and shell.</p><p>A Canon G7X digital camera was used to photograph the various organs.</p></sec><sec id="s3"><title>3. Results and Discussion</title><p>The following cephalopod species namely: Sepia dollfusi, Sepia pharaonis, Sepia elongata, Loligo forbesii, Uroteuthis Photololigo duvaucelii, Sepioteuthis lessoniana, Octopus vulgaris, Callistoctopus macropus, Macrotritopus defilippi, Amphyoctopus aegina, and Amphyoctopus membranaceus were encountered during the present study.</p><p>The following is the taxonomic order of the species that have been recorded <sup> </sup></p><p>Phylum: Mollusca;</p><p>Class: Cephalopoda Cuvie, 1798;</p><p>Subclass: Coleoidea Bather, 1888;</p><p>Superorder (A): Decapodiformes;</p><p>Order (I): Sepiida Naef, 1916;</p><p>Suborder: Sepiina;</p><p>Superfamily: Sepioidea;</p><p>Family: Sepiidae Keferstein, 1866;</p><p>Genus Sepia Linnaeus, 1758.</p><p>1) Sepia dollfusi Adam, 1941b;</p><p>2) Sepia pharaonis Ehrenberg, 1831;</p><p>3) Sepia elongata d’Orbigny, 1839-1842;</p><p>The three cuttlefish species found in Egypt’s Red Sea are Sepia dollfusi, Sepia pharaonis, and Sepia elongata.</p><p>1) Sepia dollfusi Adam, 1941:</p><p>World distribution: Red Sea waters and the Suez Canal (Nesis [<xref ref-type="bibr" rid="scirp.118258-ref20">20</xref>]);</p><p>Local name: Sobia (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Local distribution: Suez Gulf (Emam &amp; Saad [<xref ref-type="bibr" rid="scirp.118258-ref22">22</xref>]) and (Gabr &amp; Hanlon [<xref ref-type="bibr" rid="scirp.118258-ref23">23</xref>]) &amp; Suez Gulf and Red Sea (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: Sepia dollfusi dwell the Red Sea and Gulf of Suez waters (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>]).</p><p>2) Sepia pharaonis Ehrenber, 1831:</p><p>Synonymy: Sepia (Acanthosepion) pharaonis, Ehrenberg, 1831;</p><p>Worlddistribution: The IndoPacific region including the Red Sea, Arabian Sea, South China Sea, East China Sea, and northern and northern Australia (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>];</p><p>Local name: Sobia (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Local distribution: Gulf of Suez and Red Sea (Gabr et al. [<xref ref-type="bibr" rid="scirp.118258-ref24">24</xref>]);</p><p>Habitat: From the beach to around 110 metres deep, this neritic demersal species can be found. With the Upper 40 meters deep (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>]).</p><p>3) Sepia elongata: d’Orbigny, 1839-1842:</p><p>World Distribution: Indopacific and Red Sea (Nesis [<xref ref-type="bibr" rid="scirp.118258-ref20">20</xref>]);</p><p>Local name: Sobia (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Local distribution: Suez Gulf and Red Sea (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: A neritic, demersal species that can be found from the beach to around 110 metres deep, but is more;</p><p>Common in the Upper 40 meters deep (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>]).</p><p>Description</p><p>A comparison for the 3 Egyptian Red Sea cuttlefishes:</p><p>The descriptions of the specimens in hand (Tables 1-5) are in good agreement with the descriptions given by previous authors (Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>]) and (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>]).</p><p>Remarks</p><p>According to Robson [<xref ref-type="bibr" rid="scirp.118258-ref25">25</xref>], Sepia pharaonis possesses a transverse Zebra stripe pattern, which vanished in our study after preservation in formalin solution. Besides, gill was found to be 45 gill lamellae.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> External morphological features: (Plate 1)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Sepia dollfusi</th><th align="center" valign="middle" >Sepia pharaonis</th><th align="center" valign="middle" >Sepia elongata</th></tr></thead><tr><td align="center" valign="middle" >Large mantle with weak open mantle cavity. The long arms hold 4 rows of suckers (Plate 1(a)).</td><td align="center" valign="middle" >Broad mantle. Broad Fin, approximately as mantle length (Plate 1(b)).</td><td align="center" valign="middle" >Elongate body. The arms are endowed with four series of suckers, among which the averages are slightly larger than the lateral Suckers in the distal parts of the arms, first and second in males and second and third pairs in females, are in two rows (Plate 1(c)).</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula1"><graphic  xlink:href="//html.scirp.org/file/1-1470588x3.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 1. External morphological features: (a) Sepia dollfusi; (b) Sepia pharaonis; (c) Sepia elongata.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Tentacular club: (Plate 2)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Sepia dollfusi</th><th align="center" valign="middle" >Sepia pharaonis</th><th align="center" valign="middle" >Sepia elongata</th></tr></thead><tr><td align="center" valign="middle" >The tentacular club has 5 to 7 suckers in the center row that are greater than the others. Tentacular suckers of the club gradually decrease in size towards the edge of the tentacular club. The club’s protecting membranes are parallel at the carpal section and terminate on the tentacular club’s stalk (Plate 2(a)).</td><td align="center" valign="middle" >Well differentiated club. There aren’t any suckers on the stem. Eight transverse rows of suckers run across the center of the club. A few medium Suckers. (5 or 6 longitudinal suckers). The club swimming membrane is well developed, but it does not extend all the way to the stem (Plate 2(b)).</td><td align="center" valign="middle" >The club of tentacle small with a well-developed keel in length, it measures around 15% of the tentacles and holds a series of five large suckers, the other tentacular club suckers are small (Plate 2(c)).</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula2"><graphic  xlink:href="//html.scirp.org/file/1-1470588x4.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 2. Tentacular club: (a) Sepia dollfusi; (b) Sepia pharaonis; (c) Sepia elongata.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Left arm IV of male hectocotylized: (Plate 3)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Sepia dollfusi</th><th align="center" valign="middle" >Sepia pharaonis</th><th align="center" valign="middle" >Sepia elongata</th></tr></thead><tr><td align="center" valign="middle" >The left arm IV hectocotylize modified in the semi-terminal part forward by 12 transverse rows of 4 minute suckers (Plate 3(a)).</td><td align="center" valign="middle" >At the bottom of hectocotyli zed arm, there are ten rows of quadric normal suckers, followed by ten rows of ventral normal suckers. (there are two rows) (Plate 3(b)).</td><td align="center" valign="middle" >The hectocotylized arm has a special construction for a unique inflated body and is encased around a free edge. Normal suckers are present in the proximal and distal regions of the hectocotylized arm (Plate 3(c)).</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula3"><graphic  xlink:href="//html.scirp.org/file/1-1470588x5.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 3. Left arm IV of male hectocotylized: (a) Sepia dollfusi; (b) Sepia pharaonis; (c) Sepia elongata.</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> The gill: (Plate 4)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Sepia dollfusi</th><th align="center" valign="middle" >Sepia pharaonis</th><th align="center" valign="middle" >Sepia elongata</th></tr></thead><tr><td align="center" valign="middle" >The gill has Over 30 gill lamellae (Plate 4(a)).</td><td align="center" valign="middle" >The gill with about 45 gill lamellae (Plate 4(b)).</td><td align="center" valign="middle" >The gill contains 20 gill lamellae (Plate 4(c)).</td></tr></tbody></table></table-wrap><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> The shell: (Plate 5)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Sepia dollfusi</th><th align="center" valign="middle" >Sepia pharaonis</th><th align="center" valign="middle" >Sepia elongata</th></tr></thead><tr><td align="center" valign="middle" >Plate 5(a)</td><td align="center" valign="middle" >Plate 5(b)</td><td align="center" valign="middle" >Plate 5(c)</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula4"><graphic  xlink:href="//html.scirp.org/file/1-1470588x6.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 4. The gill: (a) Sepia dollfusi; (b) Sepia pharaonis; (c) Sepia elongata.</p><disp-formula id="scirp.118258-formula5"><graphic  xlink:href="//html.scirp.org/file/1-1470588x7.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 5. The shell: (a) Sepia dollfusi; (b) Sepia pharaonis; (c) Sepia elongata.</p><p>The largest sample in this study had a mantle length of 14.7 cm, while the smallest specimen had a mantle length of 9.5 cm. While according to Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>] the common size ranges from 15 to 20 cm dorsal mantle lengths. Sepia pharaonis and Sepia ramani are nearly very similar but within the sight of a lengthy club, Sepia ramani differs from Sepia pharaonis. With 15 to 24 magnifying suckers that are semi-equal in size.</p><p>Six enlarged central club suckers exist in Sepia pharaonis, three or four of which are much larger than the rest. Instead of 10 to 12 rows of hectocotylized transverse rows of normalsize suckers on the proximal end of the arm, Sepia ramani has 14 to 16 rows as in Sepia pharaonis (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>]). According to Adam [<xref ref-type="bibr" rid="scirp.118258-ref6">6</xref>] this species is easily differentiated from Sepia aculeate, by having the suckers of the two middle rows greatly enlarged.</p><p>Adam’s ( [<xref ref-type="bibr" rid="scirp.118258-ref5">5</xref>]) description of Sepia elongata is very similar to the description of the present work.</p><p>Apart from the gill, the specimens recovered from the Egyptian Red Sea feature 45-gill lamellae.</p><p>The species is recognized by its lengthy form and five suckers on the tentacular club that is substantially larger than the others. A remarkable hectocotylized arm and a shell with a hard puffed up ventral face and two broad lateral wings.</p><p>Sepia elongata has a similar club and hectocotylus to Sepia trygonina, but its shell is thicker (Jereb and Roper [<xref ref-type="bibr" rid="scirp.118258-ref17">17</xref>]).</p><p>Order (II): Myopsida d’Orbigny, 1845;</p><p>Family: Loliginidae Steenstrup, 1861;</p><p>Genus: Loligo Schneider, 1784.</p><p>1) Loligo forbesii Steemstrup, 1856:</p><p>Genus: Uroteuthis. Rehder, 1945;</p><p>Subgenus: Photololigo;</p><p>2) Uroteuthis Photololigo duvaucelii d’Orbgny, 1848:</p><p>Genus: Sepioteuthis Blainville,1824;</p><p>3) Sepioteuthis lessoniana Lsson, 1830;</p><p>Three squid species were recorded in the Egyptian Red Sea waters:</p><p>Namely: Loligo forbesii, Uroteuthis Photololigo duvaucelii, and Sepioteuthis lessoniana.</p><p>1) Loligo forbesii:</p><p>World distribution: Mediterranean sea (Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>]), North-Western Mediterranean (Boletzky &amp; Mangold [<xref ref-type="bibr" rid="scirp.118258-ref26">26</xref>]), Red Sea and East Africa (Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>]), Catalonian Sea (Sanchez [<xref ref-type="bibr" rid="scirp.118258-ref27">27</xref>]) and East of Atlantic from 20˚N to 60˚N (Except the Baltic sea) (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>]);</p><p>Local name: Kalimaria (Riad [<xref ref-type="bibr" rid="scirp.118258-ref28">28</xref>]);</p><p>Local distribution: by combing for samples from Rosetta 2 m to 36 m (Egyptian Mediterranean waters) (Riad [<xref ref-type="bibr" rid="scirp.118258-ref28">28</xref>]);</p><p>As well as fishing boats from the Red Sea and the Suez Gulf, Ataka port (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: A temperate shelf species that can be found in deep subtropical wates. Its depth ranges from 100 to 400 meters deep (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>]).</p><p>2) Uroteuthis Photololigo duvaucelii:</p><p>Synonymy: Uroteuthis duvaucelii d’Orbigny [inFerassac &amp; d’Orbegny 1835];</p><p>World distribution: The Indian Ocean, which encompasses the Red Sea and the Arabian Sea, and includes the South China Sea and the Philippine Islands, stretching eastward from Mozambique Sea, as well as northward to Taiwan, is known as the Indopacific (area of China) (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>]);</p><p>Local name: Kalimaria (Riad [<xref ref-type="bibr" rid="scirp.118258-ref28">28</xref>]);</p><p>Local distribution: Red Sea, Gulf of Suez (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: Neritic shallow water that occurs at depths between 30 and 170 meters deep (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>]).</p><p>3) Sepioteuthis lessoniana:</p><p>World distribution: The Indo-Pacific region is widespread: the Red Sea, the Arab Sea East to 160˚E, the Hawaiian Islands to the east, northern Australia, north-central Japan (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>]);</p><p>Local name: Kalimaria (Riad [<xref ref-type="bibr" rid="scirp.118258-ref28">28</xref>]);</p><p>Local distribution: Egyptian Mediterranean waters (Riad [<xref ref-type="bibr" rid="scirp.118258-ref29">29</xref>]). And from fish trawlers operating in the Suez Gulf (Ataka Harbor), Red Sea (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: A neritic species occurs from the surface down to at least 100 meters deep (Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>]).</p><p>Description</p><p>A comparison for the 3 Egyptian Red Sea squids:</p><p>The descriptions of the specimens in hand (Tables 6-10) are in good agreement with the descriptions given by previous authors Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>] and Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>].</p><p>Remarks</p><p>The morphology of Loligo forbesii taken from Egyptian Red Sea waters agrees well with Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>].</p><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> External morphological features: (Plate 6)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Loligo forbesii</th><th align="center" valign="middle" >Uroteuthis Photololigo duvaucelii</th><th align="center" valign="middle" >Sepioteuthis lessoniana</th></tr></thead><tr><td align="center" valign="middle" >Mantle slender; The fins are elongated and concave from the back, extending to about 75% of ML, arms with two rows of suckers (Plate 6(a)).</td><td align="center" valign="middle" >Relatively short mantle. Rhombic fins, just over 50% length of the mantle (Plate 6(b)).</td><td align="center" valign="middle" >Mantle Long, sturdy, about 43% wide of the mantle length extremely long balances over 90% of the length of the mantle, wide (like sepia yet a lot more wide and more strong), as wide as 73% of the length of the mantle, most prominent width happens back to the midpoint of the fins The width of the head is a lot bigger than the length of the head and it bears two oval side eyes (Plate 6(c)).</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula6"><graphic  xlink:href="//html.scirp.org/file/1-1470588x8.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 6. External morphological features: (a) Loligo forbesii; (b) Uroteuthis Photololigo duvaucelii; (c) Sepioteuthis lessoniana.</p><table-wrap id="table7" ><label><xref ref-type="table" rid="table7">Table 7</xref></label><caption><title> Tentacular club (Plate 7)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Loligo forbesii</th><th align="center" valign="middle" >Uroteuthis Photololigo duvaucelii</th><th align="center" valign="middle" >Sepioteuthis lessoniana</th></tr></thead><tr><td align="center" valign="middle" >The manus of the tentacular club are equipped with semi-equal suckers (Plate 7(a)).</td><td align="center" valign="middle" >Tentacular club with medium suckers larger than marginal suckers with 14 to 17 short, sharp teeth in sucker ring (Plate 7(b)).</td><td align="center" valign="middle" >The club of tentacle is long and stretched with 4 rows of suckers, Manus medium suckers are developed (Plate 7(c)).</td></tr></tbody></table></table-wrap><table-wrap id="table8" ><label><xref ref-type="table" rid="table8">Table 8</xref></label><caption><title> Left arm IV of male hectocotylized: (Plate 8)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Loligo forbesii</th><th align="center" valign="middle" >Uroteuthis Photololigo duvaucelii</th><th align="center" valign="middle" >Sepioteuthis lessoniana</th></tr></thead><tr><td align="center" valign="middle" >The distal piece of the left arm, IV hectocotylized is changed possesses around 35% of its length, covered with long papillae (28 - 30), decreasing in size distally (Plate 8(a)).</td><td align="center" valign="middle" >More than half of male Hectocotylized arm with two rows of large papillae (Plate 8(b)).</td><td align="center" valign="middle" >The modified part of the hectocotylized arm is formed about 1/3 to 1/4 of the arm length (Plate 8(c)).</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula7"><graphic  xlink:href="//html.scirp.org/file/1-1470588x9.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 7. The Tentacular club. (a) Loligo forbesii; (b) UroteuthisPhotololigo duvaucelii; (c) Sepioteuthis lessoniana.</p><disp-formula id="scirp.118258-formula8"><graphic  xlink:href="//html.scirp.org/file/1-1470588x10.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 8. Left arm IV of male hectocotylized: (a) Loligo forbesii; (b) Uroteuthis (Photololigo duvaucelii); (c) Sepioteuthis lessoniana.</p><table-wrap id="table9" ><label><xref ref-type="table" rid="table9">Table 9</xref></label><caption><title> Sucker rings: (Plate 9)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Loligo forbesii</th><th align="center" valign="middle" >Uroteuthis Photololigo duvaucelii</th><th align="center" valign="middle" >Sepioteuthis lessoniana</th></tr></thead><tr><td align="center" valign="middle" >Each manus sucker ring has about 16 - 20 sharp teeth but some suckers had fewer teeth (13). (Plate 9a(i)). Arm sucker ring with 20 - 30 sharp teeth, the biggest arm sucker rings with 7 to 8 teeth (Plate 9a(ii)).</td><td align="center" valign="middle" >Club sucker ring with 14 to 17 teeth, short and sharp (Plate 9b(i)): sucker ring for arm from 9 to 11 broad teeth (Plate 9b(ii)).</td><td align="center" valign="middle" >Tentacular club sucker ring (manus sucker ring) with 17 - 22 sharp teeth (Plate 9c(i)). Arm sucker ring with 20 - 25 long sharp teeth (Plate 9c(ii)).</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula9"><graphic  xlink:href="//html.scirp.org/file/1-1470588x11.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 9. The Sucker rings: (a) Loligo forbesii; (b) Uroteuthis Photololigo duvaucelii; a(i) Tentacular club sucker ring. b(i) Sucker ring of tentacular club; a(ii) Sucker rin of arm; b(ii) Sucker ring of arm; (c) Sepioteuthis lessoniana; c(i) Tentacular club sucker ring.</p><table-wrap id="table10" ><label><xref ref-type="table" rid="table1">Table 1</xref>0</label><caption><title> The shell: (Plate 10)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Loligo forbesii</th><th align="center" valign="middle" >Uroteuthis Photololigo duvaucelii</th><th align="center" valign="middle" >Sepioteuthis lessoniana</th></tr></thead><tr><td align="center" valign="middle" >(Plate 10(a))</td><td align="center" valign="middle" >(Plate 10(b))</td><td align="center" valign="middle" >(Plate 10(c))</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula10"><graphic  xlink:href="//html.scirp.org/file/1-1470588x12.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 10. The shell: (a) Loligo forbesii; (b) Uroteuthis Photololigo duvaucelii; (c) Sepioteuthis lessoniana.</p><p>It is worth noting that Riad [<xref ref-type="bibr" rid="scirp.118258-ref28">28</xref>] recorded Loligo forbesii in the Egyptian Mediterranean waters and also recorded it from the Egyptian Red Sea waters (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]).</p><p>The current study found that the features of Uroteuthis Photololigo duvaucelii are consistent with previous Research, and that the gill has more than 60 gill lamellae. The present study found that the dorsal mantle length of Uroteuthis Photololigo duvaucelii ranged from 8.6 to 15.2 cm, whereas Jereb &amp; Roper [<xref ref-type="bibr" rid="scirp.118258-ref18">18</xref>] found that the Maximum dorsal mantle length of Uroteuthis Photololigo duvaucelii is 29 cm.</p><p>Superorder (B): Octopodiformes;</p><p>Order: Octopoda Leach, 1818;</p><p>Suborder: Incirrata Grimpe, 1916;</p><p>Superfamily: Octopodoidea;</p><p>Family: Octopodidae; d’Orbigny, 1845;</p><p>Genus: Octopus Lamrck, 1798.</p><p>1) Octopus vulgaris Cuvie, 1797;</p><p>Genus: Callistoctopus Taki, 1964;</p><p>2) Callistoctopus macropus Risso, 1826;</p><p>Genus: Macrotritopus Grimpe, 1922;</p><p>3) Macrotritopus defilippi Verany, 1851;</p><p>Genus: Amphyoctopus Fisher, 1882;</p><p>4) Amphyoctopus aegina Gray, 1849;</p><p>5) Amphyoctopusus membranaceus Quoy &amp; Gaimard, 1832.</p><p>In the Egypt’s Red Sea, five octopus species have been recorded:</p><p>namely: Octopus vulgaris, Callistoctopus macropus, Macrotritopus defilippi, Amphyoctopusaegina and Amphyoctopus membranaceus;</p><p>1) Octopus vulgaris Cuvier, 1797:</p><p>World distribution: Western Mediterranean as the Adriatic Sea and the Eastern Atlantic (Roper, et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>]). Turkish spring water (Catagan &amp; Kocatas [<xref ref-type="bibr" rid="scirp.118258-ref30">30</xref>]). In the Gulf of Mexico and the Caribbean, from the island to Brazil, and from the North Sea to Cape Hope in the North Sea (Nesis [<xref ref-type="bibr" rid="scirp.118258-ref20">20</xref>]);</p><p>Local name: Okhtaboot or Folby (Riad [<xref ref-type="bibr" rid="scirp.118258-ref28">28</xref>]);</p><p>Local distribution: Egyptian Mediterranean waters. Egyptian Red Sea and Gulf of Suez (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: On sandy bottoms, muddy with gravel and also living in cavities. The depth between 10 and 300 m deep (Robson [<xref ref-type="bibr" rid="scirp.118258-ref31">31</xref>] &amp; Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>]).</p><p>2) Callistoctopus macropus Risso, 1826:</p><p>World distribution: Worldwide distributed in warm waters (Jereb et al., [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>]): Western &amp; Eastern Mediterranean and Adriatic Sea (Fisher [<xref ref-type="bibr" rid="scirp.118258-ref32">32</xref>]); Aqaba Gulf, North Atlantic, Indian Ocean, Central and Western Pacific Oceans (Adam [<xref ref-type="bibr" rid="scirp.118258-ref6">6</xref>]); North African Bank (Fisher [<xref ref-type="bibr" rid="scirp.118258-ref32">32</xref>]); Tropical species from the Atlantic Ocean; Indo-West Pacific, particularly in Bermuda and the Bahamas, Western Atlanticfrom South Florida to Brazil, the Caribbean Sea, West Africa to the Gulf of Guinea, and the Ascension and Santa Helena Islands (Nesis [<xref ref-type="bibr" rid="scirp.118258-ref20">20</xref>]);</p><p>Local name: Okhtaboot or Hebal (Riad [<xref ref-type="bibr" rid="scirp.118258-ref28">28</xref>] &amp; Riad [<xref ref-type="bibr" rid="scirp.118258-ref33">33</xref>]);</p><p>Local distribution: Egyptian Mediterranean waters (Riad [<xref ref-type="bibr" rid="scirp.118258-ref28">28</xref>]), and Egyptian Red Sea &amp; the Gulf of Suez (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: This species inhabited rocky bottoms, cracks and holes, and sometimes also on vegetative substrates (Fisher [<xref ref-type="bibr" rid="scirp.118258-ref32">32</xref>]). Benthic shoals are that can be found on reefs, reef flats, and open bottoms (Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>]);</p><p>In this study, the species was caught from the muddy sandy lands of the Suez Gulf.</p><p>3) Macrotritopus defilippi Verany, 1851:</p><p>World distribution: Mediterranean Sea, from Morocco to Angola (Eastern Atlantic), Cape Verde Islands, Western Atlantic, Bahamas, Mexico Gulf, Caribbean Sea, Brazil, Indian Ocean, Arabian Peninsula to Burma and Southwest Pacific (Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>]) (Nesis [<xref ref-type="bibr" rid="scirp.118258-ref20">20</xref>]) (Mangold [<xref ref-type="bibr" rid="scirp.118258-ref8">8</xref>]);</p><p>Local name: Okhtaboot (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Local distribution: Egyptian Mediterranean waters. And Egyptian Red Sea &amp; Gulf of Suez (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: This species is a benthic species that lives on sandy to muddy bottoms 6 to 60 meters deep (Jereb et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>]).</p><p>4) Amphyoctopus aegina Gray, 1849:</p><p>World distribution: Western Pacific, Indian Ocean, Red Sea, Japan to Mozambique from 30 to 120 meters deep (Jereb et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>]);</p><p>Local name: Okhtaboot (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Local distribution: Suez Gulf, Red Sea (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: is a benthic species with a low level of secrecy that can be found in depths of 30 to 120 metres on the continental shelf (Jereb et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>]).</p><p>5) Amphyoctopus membranaceus Quoy &amp; Gaimard, 1832:</p><p>World distribution: Indo-Pacific, Indian Ocean to Japan, China, Philippines and ward South to Australia (Jereb et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>]);</p><p>Local name: Okhtaboot (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Local distribution: Red Sea, Gulf of Suez (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]);</p><p>Habitat: A benthic shallow-water species occurring down to about 60 m. deep. It shows strong cryptic behavior and usually hides on flat bottoms (Jereb et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>]).</p><p>Description</p><p>A comparison regarding five Egyptian Red Sea octopuses:</p><p>The descriptions of the Specimens in hand (Tables 11-13) are in good agreement with the descriptions given by previous authors (Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>] &amp; (Jereb et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>]).</p><p>Remarks:</p><p>The morphology of Octopus vulgaris, Callistoctopus macropus, Macrotritopus defilippi, Amphyoctopus aegina, and Amphyoctopus membranaceus from the Egyptian Red Sea waters agrees well with that previously reported by Roper et. al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>] &amp; Jereb et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>].</p><table-wrap id="table11" ><label><xref ref-type="table" rid="table1">Table 1</xref>1</label><caption><title> External morphological features: (Plate 11)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Octopus vulgaris</th><th align="center" valign="middle" >Callistoctopus macropus</th><th align="center" valign="middle" >Macrotritopus defilippi</th><th align="center" valign="middle" >Amphyoctopus aegina</th><th align="center" valign="middle" >Amphyoctopus membranaceus</th></tr></thead><tr><td align="center" valign="middle" >octopus vulgaris’ body is round and lacks contrast With its head and arms, which are covered in flat Tubercles. Three cirri over each eye (Plate 11(a)).</td><td align="center" valign="middle" >White dots can be found on the dorsal body. The arms are abnormally lengthy, measuring 6 - 7 times the length of the body. There are two lines of suckers on each arm, with the principal pair of arms I being Substantially longer. Cirri over each eye absent (Plate 11(b)).</td><td align="center" valign="middle" >Relatively small mantle, with smooth skin, the head narrower than the mantle (Plate 11(c)).</td><td align="center" valign="middle" >Mantle round to oval, covered with minute papillae arranged in a reticular pattern, one cirri above each eye (Plate 11(d)).</td><td align="center" valign="middle" >Mantle elongate. Two cirri over each eye. Arms moderately long. (Short web, On the web at the base of arms II, anteroventral of the eyes, there is a ringed ocellus (Plate 11(e)).</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula11"><graphic  xlink:href="//html.scirp.org/file/1-1470588x13.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 11. External morphological features: (a) Octopus vulgaris; (b) Callisoctopus macropus; (c) Macrotritopus defilippi; (d) Amphyoctopu aegina; (e) Amphyoctopus membranaceus.</p><table-wrap id="table12" ><label><xref ref-type="table" rid="table1">Table 1</xref>2</label><caption><title> Male hectocotylized left arm III (Plate 12)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Octopus vulgaris</th><th align="center" valign="middle" >Callistoctopus macropus</th><th align="center" valign="middle" >Macrotritopus defilippi</th><th align="center" valign="middle" >Amphyoctopus aegina</th><th align="center" valign="middle" >Amphyoctopus membranaceus</th></tr></thead><tr><td align="center" valign="middle" >portion of a male’s third right arm modification Hectocotylize is a little spoonshaped ligula that takes up roughly 2.25% of the length of the hectocotylize (Plate 12(a)).</td><td align="center" valign="middle" >A big tubular ligula on the male’s right arm III hectocotylize, extending 13% to 15% of its length (ligula index) (Plate 12(b)).</td><td align="center" valign="middle" >The male hoctocotylize’s arm III is shorter than the opposite arm, which bears 60 - 100 suckers. Ligula is distinguished by a groove that is relatively Shallow and accounts for 1.8% to 2.5% of the hectocotylized arm length (Plate 12(c)).</td><td align="center" valign="middle" >Right arm III hectocotylizd with a short ligula, 5% to 8% of arm length, and a very shallow groove in the ligula (Plate 12(d)).</td><td align="center" valign="middle" >The male’s third right arm III hectocotylized, with a slender and lengthy ligula that accounts for 4% to 6% of arm length (Plate 12(e)).</td></tr></tbody></table></table-wrap><disp-formula id="scirp.118258-formula12"><graphic  xlink:href="//html.scirp.org/file/1-1470588x14.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 12. The right arm of the male hectocotylized: (a) Octopus vulgaris; (b) Callisoctopus macropus; (c) Macrotritopus defilippi; (d) Amphyoctopu aegina; (e) Amphyoctopus membranaceus.</p><table-wrap id="table13" ><label><xref ref-type="table" rid="table1">Table 1</xref>3</label><caption><title> The gills (Plate 13)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Octopus vulgaris</th><th align="center" valign="middle" >Callistoctopus macropus</th><th align="center" valign="middle" >Macrotritopus defilippi</th><th align="center" valign="middle" >Amphyoctopus aegina</th><th align="center" valign="middle" >Amphyoctopus membranaceus</th></tr></thead><tr><td align="center" valign="middle" >Eleven gill lamellae are present in the gill (Plate 13(a)).</td><td align="center" valign="middle" >13 gill lamellae are present in the gill (Plate 13(b)).</td><td align="center" valign="middle" >The gill with 8 - 11 gill lamellae (Plate 13(c)).</td><td align="center" valign="middle" >Seven-gill lamellae In the gill (Plate 13(d)).</td><td align="center" valign="middle" >Seven or eight-gill lamellae in the gill (Plate 13(e)).</td></tr></tbody></table></table-wrap><p>Octopus vulgaris: Arms that are shorter and a well-developed membrane between the branches distinguish Octopus vulgaris from Callistoctopus macropus.</p><p>Three cirri over each eye and up to a fifth of the length of the arms connected Except for three cirri over each eye, the anatomy of Octopus vulgaris in the current study is consistent with the publications. Forbes and Hanley [<xref ref-type="bibr" rid="scirp.118258-ref34">34</xref>] are the only ones that mentioned this character.</p><disp-formula id="scirp.118258-formula13"><graphic  xlink:href="//html.scirp.org/file/1-1470588x15.png?20220708173802595"  xlink:type="simple"/></disp-formula><p>Plate 13. The gills. (a) Octopus vulgaris; (b) Callisoctopus macropus; (c) Macrotritopus defilippi; (d) Amphyoctopu aegina; (e) Amphyoctopus membranaceus.</p><p>The largest sample collected had a total length of 104 cm. for males and 99.6 cm. for females.</p><p>Fisher [<xref ref-type="bibr" rid="scirp.118258-ref32">32</xref>] suggested a maximum overall length of 90 to 110 cm. Jereb et al. [<xref ref-type="bibr" rid="scirp.118258-ref19">19</xref>] provided larger sizes, with males’ all-out lengths of 130 cm and females’ all-out lengths of 120 cm.</p><p>2) Callistoctopus macropus: Differed from Callisoctopus macropus in the following characteristics: The morphology of Callistoctopus macropus in this study matches that of the largest specimen, which measures 16.3 cm mantle length for males and 15.9 cm mantle length for females.</p><p>Males’ total length is 138 cm while females’ is 131 cm with an absolute weight of 880 grammes for males and 625 grammes for females.</p><p>Fisher [<xref ref-type="bibr" rid="scirp.118258-ref32">32</xref>] found that related species’ maximum all-out lengths ranged from 90 to 110 cm. A total length 120 to 150 cm and mantle length of 14 cm were estimated by Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>]. The tiniest sample acquired during this evaluation revealed the estimations that accompanied it. Male’s mantle is 55 cm long, while female’s is 52 cm long.</p><p>3) Macrotritopus defilippi: It is worth noting that Riad [<xref ref-type="bibr" rid="scirp.118258-ref35">35</xref>] recorded Macrotritopus defilippi in the Egyptian Mediterranean waters and also in the Egyptian Red Sea (Riad [<xref ref-type="bibr" rid="scirp.118258-ref21">21</xref>]).</p><p>4) Amphyoctopu aegin: The morphological descriptions of Amphyoctopus aegina are very similar to those of Adam ( [<xref ref-type="bibr" rid="scirp.118258-ref5">5</xref>] and [<xref ref-type="bibr" rid="scirp.118258-ref6">6</xref>]). From the Suez Gulf and the Gulf of Aqaba the morphology of Amphyoctopus aegina in the current study is very similar to that of Amphyoctopus aegina in previous studies. Apart from Adam [<xref ref-type="bibr" rid="scirp.118258-ref6">6</xref>], who indicated that each demibranch’s gills had 8 filaments, the dorsal mantle length in the current study demonstrated the largest example to be 4.2 cm. and the smallest specimen to be 2.5 cm, although Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>] stated that the greatest dorsal mantle length is 10 cm.</p><p>5) Amphyoctopu membranaceus: The morphology of the octopus membranaceus in the current work is consistent with with the literature a parted from, gill with 7 or 8-gill lamellae and in the current work the dorsal mantle length demonstrated the biggest example to be 5.5 cm., and the smallest specimen to be 4.2 cm while according to Roper et al. [<xref ref-type="bibr" rid="scirp.118258-ref16">16</xref>] maximum mantle length is 8 cm.</p></sec><sec id="s4"><title>4. Conclusions</title><p>Cephalopods are known to be commercially important around the world. Worth mentioning it constitutes a major part of the Egyptian fishing industry. The present study aims to differentiate between cephalopod species dwelling the Egyptian Red Sea waters. Cephalopod samples were obtained from fishing vessels. Samples were photographed with a Canon G7X digital camera. Eleven Egyptian species of cephalopods are found in the Red Sea, they are:</p><p>Sepia dollfusi, Sepia pharaonis, Sepia elongata, Loligo forbesii, Uroteuthis Photololigo duvaucelii, Sepioteuthis lessoniana, Octopus vulgaris, Callistoctopus macropus, Macrotritopus defilippi, Amphyoctopus aegina and Amphyoctopus membranaceus.</p><p>Loligo forbesii and Sepioteuthis lessoniana are found in both Mediterranean and Red Sea waters of Egypt. It is worth noting that though Sepioteuthis lessonian is a Red Sea species proper, it succeeded to traverse the Suez Canal and inhabits the Egyptian Mediterranean waters. Lessepian migration is still going on as some Red Sea cephalopod species were encountered in the Egyptian Mediterranean waters.</p></sec><sec id="s5"><title>Acknowledgements</title><p>I’m thankful to my student Dr. Noha Elebiary lecture of Marine Invertebrates, National Institute of Oceanography and Fisheries for her kind supervision and cooperation throughout this work.</p><p>I wish also to thank the technical assistant Mr. Mahmoud Rezk, National Institute of Oceanography and Fisheries for his help in collecting the samples during this work.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The author declares no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Riad, R. (2022) Comparative Taxonomical Studies on the Egyptian Red Sea Cephalopods (Cephalopoda: Mollusca). 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