<?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">GEP</journal-id><journal-title-group><journal-title>Journal of Geoscience and Environment Protection</journal-title></journal-title-group><issn pub-type="epub">2327-4336</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/gep.2017.511005</article-id><article-id pub-id-type="publisher-id">GEP-80182</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>
 
 
  Hydrothermal Alterations in Irbiben Gold Deposit (Tagragra Akka, Western Anti-Atlas, Morocco): Petrographic and Geochemical Characterization
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tokpa</surname><given-names>Kakeu Lionel-Dimitri Boya</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>N’Guessan</surname><given-names>Nestor Houssou</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>Marc</surname><given-names>Ephrem Allialy</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>Allou</surname><given-names>Gnanzou</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>Lamia</surname><given-names>Erraioui</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Benyounes</surname><given-names>Maamar</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Souad</surname><given-names>M. Rabet</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Managem Group, Tower A, Twin Center, Casablanca, Morocco</addr-line></aff><aff id="aff2"><addr-line>Georesources and Environment Laboratory, Department of Geology, Faculty of Sciences, University Ibn Tofail, Kenitra, Morocco</addr-line></aff><aff id="aff1"><addr-line>Geology of Basement and Metallogeny Laboratory (GBML), Training and Research Unit of Earth Sciences and Mining Resources, University of Felix HOUPHOUET-BOIGNY, Abidjan-Cocody, C&amp;amp;#244te d’Ivoire</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>lionelboya2000@yahoo.fr(TKLB)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>02</day><month>11</month><year>2017</year></pub-date><volume>05</volume><issue>11</issue><fpage>46</fpage><lpage>60</lpage><history><date date-type="received"><day>29,</day>	<month>September</month>	<year>2017</year></date><date date-type="rev-recd"><day>5,</day>	<month>November</month>	<year>2017</year>	</date><date date-type="accepted"><day>8,</day>	<month>November</month>	<year>2017</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>
 
 
  Irbiben is a small gold deposit of the Precambrian inlier Tagragra d’Akka located in the Moroccan western Anti-Atlas, approximately 160 km southeast from Tiznit. Petrographic study shows that host rocks of Irbiben deposit are green schist facies metamorphic rocks, like metamorphic sandstone and schist, meta-pelite and quartzite. Gold is located in quartz veins or host rock with frequent injections of quartz. The petrographic characterization of alteration through the description of the alteration profiles and the comparative study of protolith and altered rocks showed a development of dominant quartz and calcite in mineralization wall-rocks. In moving away from it, there is rather sericite and chlorite. These phenomena are materialized respectively by the development of SiO
  <sub>2</sub> and CaO in the wall-rocks but rather that ferromagnesian elements (FeO, MgO) and K
  <sub>2</sub>O away from the mineralization. These trends were demonstrated by the geochemical study through Harker diagrams, description of alteration profiles, comparative study of protolith and altered rocks, and use of a new alteration index, MIA, elaborated during this work.
 
</p></abstract><kwd-group><kwd>Irbiben Gold Deposit</kwd><kwd> Hydrothermal Alteration</kwd><kwd> Petrography</kwd><kwd> Geochemistry</kwd><kwd> Morocco</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The Irbiben gold deposit, formerly operated by the Akka Mine, is located in the Akka Tagragra inlier. It is located about 160 km Southeast Tiznit city, in the Western part of the Moroccan Anti-Atlas. This area is known for its numerous deposits, including the Imiter and Zgounder silver deposits as well as the Tiouit gold deposit. The inlier, outside Irbiben, also allowed the exploitation of gold in other sites such as Iourirn, Ifarar and Angarf.</p><p>As part of our missions in this area, we have made some observations: the presence of traces of hydrothermal activity in the wall rock of the mineralization. Indeed, in addition to the deformation caused by the placement of the gold-bearing quartz veins in the host rocks, a change, however minor, affects these in their mineralogy and their chemistry. This is why this paper proposes to identify and characterize this hydrothermalism through a petrographic and geochemical study of alteration.</p><p>This work deals with the study of hydrothermal alterations in Irbiben. Several studies [<xref ref-type="bibr" rid="scirp.80182-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.80182-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.80182-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.80182-ref4">4</xref>] have shown that there are close links between the development of gold mineralization and hydrothermal alterations. Indeed, this type of association occurs in deposits of the Tagragra of Akka [<xref ref-type="bibr" rid="scirp.80182-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.80182-ref5">5</xref>] of which Irbiben is a part of.</p></sec><sec id="s2"><title>2. Global Geological Framework and Location</title><p>Morocco is subdivided into several structural domains which are from north to south: the Rifain domain, the Mesetian domain, the Atlasic domain, the Anti-Atlasic domain and the Saharan domain. Our study area is located in the Akka Tagragra inlier which is part of the Western Anti-Atlas area (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>This inlier is made of a Precambrian basement and a slightly deformed Palaeozoic cover. The Irbiben deposit is located in its eastern part (<xref ref-type="fig" rid="fig2">Figure 2</xref>), to</p><p>the south of the large ENE shear-zone crossing through much of the inlier, about 20 kilometers from the Iourirn mining center.</p></sec><sec id="s3"><title>3. Lithology</title><p>The Irbiben deposit consists of rocks of both sedimentary and magmatic origin, with mineralization hosted in the sedimentary rocks. The age of the host is attributed to the Paleo-Proterozoic [<xref ref-type="bibr" rid="scirp.80182-ref7">7</xref>] .</p><p>The sedimentary rocks consist of greywacke and sandstone alternating on a metric scale with pelites (<xref ref-type="fig" rid="fig3">Figure 3</xref>). These formations have been affected by the known epizonal metamorphism in the region, hence the presence of meta-sandstones, meta-greywacke, meta-pelites, quartzites and sandy shales in places. The sandstone material is dark gray and the pelites are black in color. The sandstone schist is distinguished from the other formations by their degree of schistosity. Meta-sandstones are sometimes deformed and injected with quartz. They can be mineralized. All these formations of the base are affected by the schistosity S<sub>1</sub> which follows the stratification S<sub>0</sub>, forming a fabric S<sub>0</sub>S<sub>1</sub> of medium direction N60. The schistosity S<sub>2</sub> is observed in several places and of direction near from N10 to N15. Some meta-sandstones are crossed by carbonate veins.</p><p>The proportion of quartz of certain silicified sandstones where the effects of regional epizonal metamorphism have not been detected, their hardness and their appearance make it possible to assimilate them to greywacke.</p><p>Magmatic rocks consist of diorite and quartz micro-diorite outcropping in the form of dykes, aplite vein and massive granite.</p><p>The dykes are scattered in the deposit near the mineralized structures and further in the southern part of the deposit where they are in contact with the</p><p>granite. They are generally of direction neighboring N40 to N60. Those in the southern part of the deposit have no direct link with the mineralization. Their thickness varies between ten to twenty meters and their variable extension can reach hundreds of meters.</p><p>The granite outcrops in the form of a massif. It presents in some places a clear limit with the dyke, of direction between N30 and N50. It intrudes the meta-sedimentary formations of the PI basement and occupies all the rest of the southern part of the eastern lobe of the inlier. Mortaji [<xref ref-type="bibr" rid="scirp.80182-ref8">8</xref>] assimilates it to granite with biotite or biotite and secondary muscovite.</p><p>The aplite there is lode, located in an intermediate zone between the granite and the dyke.</p></sec><sec id="s4"><title>4. Materials and Methods</title><p>Twelve (12) samples were taken from the cross-bed siding at the level −70 m (TB-70), then in operation. They are designated A, B ... up to L (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Eight samples designated IRBC43A to IRBC43H were also taken from the IRBC43 drill core that intersected the host formations and the NE gold quartz vein.</p><p>The petrographic study required a macroscopic and then microscopic flap, after preparation of thin plates.</p><p>Eight (8) samples were subjected to inductively coupled plasma mass spectrometric (ICP-MS) at the REMINEX research center of the MANAGEM group in Marrakech. These are two samples from the NE1 Irbiben structure of the −70 level and six from its vein wall and of the host on the sides of the vein.</p><p><xref ref-type="fig" rid="fig3">Figure 3</xref> shows the geological mapping of the southern cross-bench facing (TB-70), with the location of the samples taken and the gold structure.</p></sec><sec id="s5"><title>5. Results and Discussions: Characterization of Hydrothermal Alterations</title><sec id="s5_1"><title>5.1. Alteration Petrography</title><sec id="s5_1_1"><title>5.1.1. Alteration Profiles Description</title><p>The study of alteration profiles in the Irbiben deposit required the prior observation of the hosting rocks crossed by the gold-bearing structure. <xref ref-type="table" rid="table1">Table 1</xref> summarizes the results of the IRBC16 and IRBC43 drilling cores observations, in particular areas intersected by the gold structure.</p><p>The IRBC16 drilling intersects three gold levels. The first is materialized by a massive vein of smoky white quartz, arsenopyrite, pyrite and fine gold visible to the naked eye, while the second and the last correspond to a set of veins of smoky white quartz with arsenopyrite, pyrite and chalcopyrite carried by metapelites. The first gold level crosses a quartzite and the other two are hosted in metapelites.</p><p>The IRBC43 drilling intersects two gold levels. The first is a white gray quartz vein, brecciated, with pyrrhotite, pyrite, chlorite and sericite. Its fractures are filled with oxides and it crosses a metasandstone formation. The second gold level is rather a silicified meta-sandstone with numerous injections of gray quartz associated with carbonates. It is also with oxides, sericite, chlorite, pyrite, pyrrhotite and arsenopyrite. It marks a boundary between a metasandstone rock and a graphitized black metapelite.</p><p>These observations show the existence of different auriferous structures of the quartz veins. It is the host, metasandstone or metapelitic, with numerous injections of mineralized quartz.</p><p>The hydrothermal activity associated with the placement of the gold vein influenced the host rocks. This is reflected in an increase in their silica rate and an iron intake. This contribution is materialized by the deposition of ferriferous sulphide minerals such as arsenopyrite, pyrite or chalcopyrite that accompany the deposition of gold mineralization. The complete observation of the cores showed that the highest gold grades were found in the vein levels, where they could reach 14 g/t for the IRBC43 drilling or 13 g/t for IRBC16. The grades found in the metasedimentary material are less important, oscillating between 1 and 4 g/t.</p><p>Mineralized veins are mainly composed of silica and carbonates. This explains why the host rock affected by the hydrothermal fluid underwent enrichment in these elements, materialized by more developed quartz and calcite in the vicinity of the gold zone. The placement of the vein was also at the origin of the deformation detected in the host and materialized by a mylonitization.</p></sec><sec id="s5_1_2"><title>5.1.2. Petrographical Characterization of Alteration</title><p>The mineralogical changes between the host rock and the wallrock of the gold vein reflect the decreasing impact of the hydrothermal fluid on the host by moving away from the vein. This is why we choose to highlight the comparative</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Synthesis of the macroscopic study of core drillings crossing the Irbiben NE1 gold structure and the meta-sedimentary host in the Irbiben deposit</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Core rilling</th><th align="center" valign="middle" >Level</th><th align="center" valign="middle" >Crossed old vein</th><th align="center" valign="middle" >Macroscopic description of the facies</th></tr></thead><tr><td align="center" valign="middle"  rowspan="9"  >IRBC16</td><td align="center" valign="middle"  rowspan="3"  >19 to 23 m</td><td align="center" valign="middle"  rowspan="3"  ></td><td align="center" valign="middle" >Superior hanging wall (ROOF) Quartzite with quartz vein and chlorite</td></tr><tr><td align="center" valign="middle" >GOLD STRUCTURE Smoky white quartz with traces of arsenopyrite, pyrite and presence of very fine visible gold</td></tr><tr><td align="center" valign="middle" >Lower hanging wall (WALL) Quartzite rich in white quartz lodes, with pyrite, arsenopyrite and chalcopyrite filaments</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >36 to 41 m</td><td align="center" valign="middle"  rowspan="3"  ></td><td align="center" valign="middle" >ROOF Mylonitized black metaplite very rich in smoky white quartz lode and veinlets, very rich in arsenopyrite, pyrite and chalcopyrite</td></tr><tr><td align="center" valign="middle" >GOLD STRUCTURE Smoky white quartz lodes and veinlets with arsenopyrite, pyrite and chalcopyrite, hosted in metapelites</td></tr><tr><td align="center" valign="middle" >WALL Black metapelite with pyrite quartz lodes, chalcopyrite and traces of arsenopyrite</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >47 to 50 m</td><td align="center" valign="middle"  rowspan="3"  ></td><td align="center" valign="middle" >ROOF Black metaplite with quartz veinlets, arsenopyrite and rich in pyrite</td></tr><tr><td align="center" valign="middle" >GOLD STRUCTURE Graphitized black metaplite rich in white quartz lodes with arsenopyrite, abundant pyrite and chalcopyrite</td></tr><tr><td align="center" valign="middle" >WALL Pelitic meta-sandstone</td></tr><tr><td align="center" valign="middle"  rowspan="6"  >IRBC43</td><td align="center" valign="middle"  rowspan="3"  >120 to 123 m</td><td align="center" valign="middle"  rowspan="3"  ></td><td align="center" valign="middle" >ROOF Meta-sandstone with frequent injections of quartz deformed and oxidized with pyrrhotite and pyrite. Presence of chlorite and traces of carbonates</td></tr><tr><td align="center" valign="middle" >GOLD STRUCTURE Oxidized and brecciated white gray quartz gray in its cracks, with chlorite, sericite, pyrrhotite, pyrite. Presence of very fine gold difficult to observe</td></tr><tr><td align="center" valign="middle" >WALL Crushed and mylonitized meta-sandstone, with quartz injections in places</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >127 to 129 m</td><td align="center" valign="middle"  rowspan="3"  ></td><td align="center" valign="middle" >ROOF Meta-sandstone with frequent injections of deformed white gray quartz,with chlorite, sericite, pyrrhotite, pyrite, carbonate in traces and oxidation of iron in quartz veinlets</td></tr><tr><td align="center" valign="middle" >GOLD STRUCTURE Highly silicified meta-sandstone with gray quartz and carbonates, oxides, sericite, chlorite, abundant arsenopyrite, pyrrhotite and pyrite</td></tr><tr><td align="center" valign="middle" >WALL Graphitized black metaplite, with brecciated quartz veins, pyrite, pyrrhotite and arsenopyrite</td></tr></tbody></table></table-wrap><p>microscopic study of two samples, one considered as control rock and the other as altered rock.</p><p>The protolith is located 3 m from the gold vein. This is sample D. It is a me- tagreywacke composed of quartz, healthy plagioclases and micas. Automorphic and sub-automorphic quartz and plagioclases have an initial orientation. Micas are interstitial.</p><p>The altered rock constitutes the wall of the mineralization (sample F). This is a distorted meta-greywacke. It contains much more quartz, fewer healthy plagioclases, most of which are altered, sericite, chlorite, calcite and epidote.</p><p>Observing also the mineralized vein (sample L), we find that it is essentially dominant quartz and calcite. The altered rock contains, in addition to the minerals of the control rock, new minerals such as well-developed calcite and epidote. Furthermore, the proportions of the minerals common to both samples vary in terms of the distance to the vein. Sericite and chlorite have higher grades in the hanging wall. These observations are illustrated in <xref ref-type="fig" rid="fig4">Figure 4</xref>.</p><p>By approaching the vein, the host is enriched much more in quartz and calcite than in sericite and chlorite. The host is metasedimentary, which explains the presence of sericite and chlorite in its composition. However, in contact with the vein, it knows enrichment in these minerals. The hydrothermalism accompany- ing the placement of the vein influences the composition of the host rock by a contribution of silica and carbonates materialized by the appearance of quartz Q<sub>III</sub> and calcite or the development of quartz Q<sub>II</sub>. Alteration sericite originates essentially from the destabilization of pre-existing minerals such as plagioclases and chlorite comes from a neo-formation of minerals accompanying deposition of the mineralization. The various alterations are silicification which is the most important and which is associated with calcitization, sericitization and chloritization. Hanging walls are more marked by silicification and calcitization. These phenomena have already been observed in the Ifarar deposit [<xref ref-type="bibr" rid="scirp.80182-ref5">5</xref>] .</p></sec></sec><sec id="s5_2"><title>5.2. Alteration Geochemistry</title><p>The oxide weight grades of the samples analyzed show notable variations for some, in particular SiO<sub>2</sub>, for which they are between 82.49% and 54.52% (<xref ref-type="table" rid="table2">Table 2</xref>). The highest grade characterizes the gold vein and, on the mineralogical level, it is represented by an abundance of quartz minerals, in the form of 3 distinct petty-types. The quartz Q<sub>III</sub> which is the most recent and resulting from the hydrothermal alteration is the most represented. From the host rock to gold structure, the amount of quartz of the rocks increases, which is corroborated by the geochemical analyzes which show a gradual increase of SiO<sub>2</sub> of 54.52% in the host rock to values reaching 64.57% in the hanging wall to be maximum in the vein (78.45% and 82.49%). This increase is caused by the interaction of the hydrothermal fluid at the origin of the aqueous silica supply as in the Ifarar deposit [<xref ref-type="bibr" rid="scirp.80182-ref5">5</xref>] . This influence is materialized on the ground by a silicification, more important in the level of the hanging walls and which is translated by a predominance of hydrothermal quartz Q<sub>III</sub>.</p><p>Except for CaO and MnO grades that increase with the SiO<sub>2</sub> grade in the rock, the other analyzed oxides show downward tendencies as they move closer to the gold vein (<xref ref-type="fig" rid="fig5">Figure 5</xref>).</p><p>To understand better the impact of the gold vein on its host rock, an average of the oxide weight grades was calculated for samples from rocks equidistant from the vein on both sides. The evolution has therefore been followed from the gold-bearing structure, passing through the hanging wall to the more distant rocks. These new calculated grades are presented in <xref ref-type="table" rid="table3">Table 3</xref>.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Geochemical analyzes in major elements of Irbiben samples</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  ></th><th align="center" valign="middle"  colspan="2"  >Host</th><th align="center" valign="middle" >Wall rock</th><th align="center" valign="middle" >Wall rock</th><th align="center" valign="middle"  colspan="2"  >Host</th><th align="center" valign="middle"  colspan="2"  >Gold vein</th></tr></thead><tr><td align="center" valign="middle" >D</td><td align="center" valign="middle" >E</td><td align="center" valign="middle" >F</td><td align="center" valign="middle" >H</td><td align="center" valign="middle" >I</td><td align="center" valign="middle" >J</td><td align="center" valign="middle" >L1</td><td align="center" valign="middle" >L2</td></tr><tr><td align="center" valign="middle" >SiO<sub>2</sub></td><td align="center" valign="middle" >62.38</td><td align="center" valign="middle" >58.92</td><td align="center" valign="middle" >61.79</td><td align="center" valign="middle" >64.57</td><td align="center" valign="middle" >57.05</td><td align="center" valign="middle" >54.52</td><td align="center" valign="middle" >78.45</td><td align="center" valign="middle" >82.49</td></tr><tr><td align="center" valign="middle" >TiO<sub>2</sub></td><td align="center" valign="middle" >0.77</td><td align="center" valign="middle" >0.79</td><td align="center" valign="middle" >0.63</td><td align="center" valign="middle" >0.62</td><td align="center" valign="middle" >0.76</td><td align="center" valign="middle" >0.86</td><td align="center" valign="middle" >0.24</td><td align="center" valign="middle" >0.12</td></tr><tr><td align="center" valign="middle" >Al<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >16.11</td><td align="center" valign="middle" >18.01</td><td align="center" valign="middle" >13.18</td><td align="center" valign="middle" >15.77</td><td align="center" valign="middle" >20.14</td><td align="center" valign="middle" >20.99</td><td align="center" valign="middle" >6.46</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >Fe<sub>2</sub>O<sub>3</sub>*</td><td align="center" valign="middle" >0.66</td><td align="center" valign="middle" >0.72</td><td align="center" valign="middle" >0.83</td><td align="center" valign="middle" >0.51</td><td align="center" valign="middle" >0.57</td><td align="center" valign="middle" >0.62</td><td align="center" valign="middle" >0.39</td><td align="center" valign="middle" >0.33</td></tr><tr><td align="center" valign="middle" >FeO<sub>calculated</sub></td><td align="center" valign="middle" >5.9</td><td align="center" valign="middle" >6.37</td><td align="center" valign="middle" >7.39</td><td align="center" valign="middle" >4.51</td><td align="center" valign="middle" >5.04</td><td align="center" valign="middle" >5.54</td><td align="center" valign="middle" >3.52</td><td align="center" valign="middle" >2.93</td></tr><tr><td align="center" valign="middle" >FeOtot</td><td align="center" valign="middle" >6.56</td><td align="center" valign="middle" >7.09</td><td align="center" valign="middle" >8.22</td><td align="center" valign="middle" >5.02</td><td align="center" valign="middle" >5.61</td><td align="center" valign="middle" >6.16</td><td align="center" valign="middle" >3.91</td><td align="center" valign="middle" >3.26</td></tr><tr><td align="center" valign="middle" >MnO</td><td align="center" valign="middle" >0.04</td><td align="center" valign="middle" >0.04</td><td align="center" valign="middle" >0.07</td><td align="center" valign="middle" >0.04</td><td align="center" valign="middle" >0.03</td><td align="center" valign="middle" >0.03</td><td align="center" valign="middle" >0.06</td><td align="center" valign="middle" >0.08</td></tr><tr><td align="center" valign="middle" >MgO</td><td align="center" valign="middle" >4.15</td><td align="center" valign="middle" >4.38</td><td align="center" valign="middle" >4.57</td><td align="center" valign="middle" >3.27</td><td align="center" valign="middle" >3.69</td><td align="center" valign="middle" >3.88</td><td align="center" valign="middle" >1.4</td><td align="center" valign="middle" >1.24</td></tr><tr><td align="center" valign="middle" >CaO</td><td align="center" valign="middle" >0.22</td><td align="center" valign="middle" >0.4</td><td align="center" valign="middle" >1.73</td><td align="center" valign="middle" >0.39</td><td align="center" valign="middle" >0.15</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >2.5</td><td align="center" valign="middle" >3.78</td></tr><tr><td align="center" valign="middle" >Na<sub>2</sub>O</td><td align="center" valign="middle" >0.97</td><td align="center" valign="middle" >0.31</td><td align="center" valign="middle" >0.19</td><td align="center" valign="middle" >0.18</td><td align="center" valign="middle" >0.3</td><td align="center" valign="middle" >0.33</td><td align="center" valign="middle" >0.14</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >K<sub>2</sub>O</td><td align="center" valign="middle" >3.27</td><td align="center" valign="middle" >4.35</td><td align="center" valign="middle" >2.84</td><td align="center" valign="middle" >4.58</td><td align="center" valign="middle" >5.99</td><td align="center" valign="middle" >6.03</td><td align="center" valign="middle" >1.9</td><td align="center" valign="middle" >0.71</td></tr><tr><td align="center" valign="middle" >P<sub>2</sub>O<sub>5</sub></td><td align="center" valign="middle" >0.09</td><td align="center" valign="middle" >0.09</td><td align="center" valign="middle" >0.08</td><td align="center" valign="middle" >0.09</td><td align="center" valign="middle" >0.09</td><td align="center" valign="middle" >0.1</td><td align="center" valign="middle" >0.04</td><td align="center" valign="middle" >0.02</td></tr><tr><td align="center" valign="middle" >PF</td><td align="center" valign="middle" >4.13</td><td align="center" valign="middle" >4.71</td><td align="center" valign="middle" >4.93</td><td align="center" valign="middle" >4.47</td><td align="center" valign="middle" >4.96</td><td align="center" valign="middle" >5.47</td><td align="center" valign="middle" >3.78</td><td align="center" valign="middle" >3.83</td></tr><tr><td align="center" valign="middle" >FeO + MgO</td><td align="center" valign="middle" >10.71</td><td align="center" valign="middle" >11.47</td><td align="center" valign="middle" >12.79</td><td align="center" valign="middle" >8.29</td><td align="center" valign="middle" >9.3</td><td align="center" valign="middle" >10.04</td><td align="center" valign="middle" >5.31</td><td align="center" valign="middle" >4.5</td></tr><tr><td align="center" valign="middle" >Na<sub>2</sub>O + K<sub>2</sub>O</td><td align="center" valign="middle" >4.24</td><td align="center" valign="middle" >4.66</td><td align="center" valign="middle" >3.03</td><td align="center" valign="middle" >4.76</td><td align="center" valign="middle" >6.29</td><td align="center" valign="middle" >6.36</td><td align="center" valign="middle" >2.04</td><td align="center" valign="middle" >0.81</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Mean oxide grades calculated for samples situated at the same distance from the gold vein</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Vein Au (L)</th><th align="center" valign="middle" >Wall rock F − H</th><th align="center" valign="middle" >E − I (2 m)</th><th align="center" valign="middle" >D − J (3 m)</th></tr></thead><tr><td align="center" valign="middle" >SiO<sub>2</sub></td><td align="center" valign="middle" >80.47</td><td align="center" valign="middle" >63.18</td><td align="center" valign="middle" >57.985</td><td align="center" valign="middle" >58.45</td></tr><tr><td align="center" valign="middle" >TiO<sub>2</sub></td><td align="center" valign="middle" >0.18</td><td align="center" valign="middle" >0.625</td><td align="center" valign="middle" >0.775</td><td align="center" valign="middle" >0.815</td></tr><tr><td align="center" valign="middle" >Al<sub>2</sub>O<sub>3</sub></td><td align="center" valign="middle" >4.73</td><td align="center" valign="middle" >14.475</td><td align="center" valign="middle" >19.075</td><td align="center" valign="middle" >18.55</td></tr><tr><td align="center" valign="middle" >Fe<sub>2</sub>O<sub>3</sub>*</td><td align="center" valign="middle" >0.36</td><td align="center" valign="middle" >0.67</td><td align="center" valign="middle" >0.645</td><td align="center" valign="middle" >0.64</td></tr><tr><td align="center" valign="middle" >FeO<sub>calculated</sub></td><td align="center" valign="middle" >3.225</td><td align="center" valign="middle" >5.95</td><td align="center" valign="middle" >5.705</td><td align="center" valign="middle" >5.72</td></tr><tr><td align="center" valign="middle" >FeO<sub>tot</sub></td><td align="center" valign="middle" >3.585</td><td align="center" valign="middle" >6.62</td><td align="center" valign="middle" >6.35</td><td align="center" valign="middle" >6.36</td></tr><tr><td align="center" valign="middle" >MnO</td><td align="center" valign="middle" >0.07</td><td align="center" valign="middle" >0.055</td><td align="center" valign="middle" >0.035</td><td align="center" valign="middle" >0.035</td></tr><tr><td align="center" valign="middle" >MgO</td><td align="center" valign="middle" >1.32</td><td align="center" valign="middle" >3.92</td><td align="center" valign="middle" >4.035</td><td align="center" valign="middle" >4.015</td></tr><tr><td align="center" valign="middle" >CaO</td><td align="center" valign="middle" >3.14</td><td align="center" valign="middle" >1.06</td><td align="center" valign="middle" >0.275</td><td align="center" valign="middle" >0.16</td></tr><tr><td align="center" valign="middle" >Na<sub>2</sub>O</td><td align="center" valign="middle" >0.12</td><td align="center" valign="middle" >0.185</td><td align="center" valign="middle" >0.305</td><td align="center" valign="middle" >0.65</td></tr><tr><td align="center" valign="middle" >K<sub>2</sub>O</td><td align="center" valign="middle" >1.305</td><td align="center" valign="middle" >3.71</td><td align="center" valign="middle" >5.17</td><td align="center" valign="middle" >4.65</td></tr><tr><td align="center" valign="middle" >P<sub>2</sub>O<sub>5</sub></td><td align="center" valign="middle" >0.03</td><td align="center" valign="middle" >0.085</td><td align="center" valign="middle" >0.09</td><td align="center" valign="middle" >0.095</td></tr><tr><td align="center" valign="middle" >PF</td><td align="center" valign="middle" >3.805</td><td align="center" valign="middle" >4.7</td><td align="center" valign="middle" >4.835</td><td align="center" valign="middle" >4.8</td></tr><tr><td align="center" valign="middle" >FeO + MgO</td><td align="center" valign="middle" >4.905</td><td align="center" valign="middle" >10.54</td><td align="center" valign="middle" >10.385</td><td align="center" valign="middle" >10.375</td></tr><tr><td align="center" valign="middle" >Na<sub>2</sub>O + K<sub>2</sub>O</td><td align="center" valign="middle" >1.425</td><td align="center" valign="middle" >3.895</td><td align="center" valign="middle" >5.475</td><td align="center" valign="middle" >5.3</td></tr></tbody></table></table-wrap><p>Al<sub>2</sub>O<sub>3</sub> is considered immobile during alteration. The apparent variation of its grade is only a reflection of the mobility of the other components of the host rocks, such as FeO<sub>tot</sub>, K<sub>2</sub>O or CaO.</p><p>The ferromagnesian (Fe + Mg) grades of the rocks are associated with the proportion of ferromagnesian minerals such as chlorite (corresponding oxides: FeO<sub>tot</sub> and MgO) and sericite (K<sub>2</sub>O). The highest oxide grade by weight corresponds to the hanging wall. However, the initial rock is potentially rich in these oxides, with about 10.38%. The gold vein presents the lowest grade which is of 4.9%. Although the difference in grade between the gold vein and its hanging wall is significant (from 4.9% to 10.54%), it is not significant, as the rock is already rich in these oxides. This increase is due to a destabilization of the minerals of the host, such as plagioclases, the alteration of which produces sericite, which increases its proportion in the hanging walls. Moreover, the deposition of the mineralization is accompanied by the neo-formation of chlorite minerals. It is a previously observed iron chlorite and is described in other deposits of the Tagragra Akka inlier [<xref ref-type="bibr" rid="scirp.80182-ref3">3</xref>] . An increase in the proportion of chlorite in host rock causes in the hanging wall an increase in the grade of FeO<sub>tot</sub> and MgO (<xref ref-type="table" rid="table3">Table 3</xref>), which corresponds to the analyzed and calculated grades. The plagioclases alteration which produces sericite and the neo-formation of ferric chlorite are hydrothermal events corresponding respectively to sericitization and chloritization of the host.</p><p>However, sericitization is much more related to the variation of alkalis elements, which increase significantly between the gold vein (1.42%) and the hanging wall (3.89%). The formed sericite mobilizes more K<sub>2</sub>O and Al<sub>2</sub>O<sub>3</sub> than ferromagnesians which are associated with chlorite. The highest grades of alkaline (Na<sub>2</sub>O + K<sub>2</sub>O), which are 5.3% and 5.47%, characterize the host rock originally formed from minerals containing potassium such as sericite or muscovite.</p><p>For the host rocks, the CaO grades varying from 0.16% to 0.27% are lower than that of the hanging walls, which is 1.06% (<xref ref-type="table" rid="table3">Table 3</xref> and <xref ref-type="fig" rid="fig6">Figure 6</xref>). The highest grade is 3.14% and is associated with the gold vein.</p><p>In Irbiben, the gold quartz vein is predominantly composed of quartz, associated with calcite, as shown by the microscopic study (<xref ref-type="fig" rid="fig4">Figure 4</xref>). The lowest grades in host rock show a lack of calcite. The CaO grade of the vein and that of</p><p>the hanging wall reveal the influence of the hydrothermal fluid on host rock by a carbonate supply. The orogenic gold deposits are characterized by aquo-carbonic fluids [<xref ref-type="bibr" rid="scirp.80182-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.80182-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.80182-ref11">11</xref>] and their circulation is almost always associated with the addition of CO<sub>2</sub>, K and S, with a slight addition or loss of other major elements [<xref ref-type="bibr" rid="scirp.80182-ref9">9</xref>] . The presence of carbonates has also been reported, associated with the quartz of these veins [<xref ref-type="bibr" rid="scirp.80182-ref12">12</xref>] . In Irbiben deposit, the mineralogical changes observed in the host rock make it possible to suspect a fluid of this type. Its interaction with the initial calcium (detected by geochemical analysis) of the host rocks caused the formation of hydrothermal calcite in the hanging walls, by alteration of the plagioclases. The formation of hydrothermal calcite in the deposit corresponds to calcitization.</p><p>The mobility of trace elements such as boron, barium, strontium and lead should be considered in the study of hydrothermal alterations. <xref ref-type="table" rid="table4">Table 4</xref> presents the correlations between the major elements and significant traces in the study of the alteration.</p><p>Boron which is generally associated with hydrothermal minerals has good correlations with K<sub>2</sub>O (0.82) and FeO<sub>tot</sub> (0.68). In the Irbiben deposit, in addition to the ferrous sulphide minerals, some hydrothermal minerals may be ferriferous, such as the chlorite which accompanies mineralization. Changes in K<sub>2</sub>O are associated with sericitization. Boron associates with sericite and chlorite, which explains its high grades in the host rocks of the deposit (101 ppm to 123 ppm), except in the vein where values are very low (31 ppm to 52 ppm).</p><p>Barium has also a good correlation with TiO<sub>2</sub>, FeO<sub>tot</sub> and K<sub>2</sub>O. These oxides have their grades which increase with the alteration. Its strong negative correlation with calcium (−0.80) reflects the significant substitution of calcium from the host rocks by barium. This explains why the host rocks are not rich in calcite.</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Correlations matrix between major elements and traces revealing the alteration</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >SiO<sub>2</sub></th><th align="center" valign="middle" >TiO<sub>2</sub></th><th align="center" valign="middle" >FeO<sub>tot</sub></th><th align="center" valign="middle" >MnO</th><th align="center" valign="middle" >MgO</th><th align="center" valign="middle" >CaO</th><th align="center" valign="middle" >Na<sub>2</sub>O</th><th align="center" valign="middle" >K<sub>2</sub>O</th><th align="center" valign="middle" >P<sub>2</sub>O<sub>5</sub></th><th align="center" valign="middle" >B</th><th align="center" valign="middle" >Ba</th><th align="center" valign="middle" >Pb</th><th align="center" valign="middle" >Sr</th></tr></thead><tr><td align="center" valign="middle" >SiO<sub>2</sub></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >TiO<sub>2</sub></td><td align="center" valign="middle" >−0.97</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Fe<sub>2</sub>O<sub>tot</sub></td><td align="center" valign="middle" >−0.76</td><td align="center" valign="middle" >0.70</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >MnO</td><td align="center" valign="middle" >0.39</td><td align="center" valign="middle" >−0.42</td><td align="center" valign="middle" >−0.18</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >MgO</td><td align="center" valign="middle" >−0.64</td><td align="center" valign="middle" >0.71</td><td align="center" valign="middle" >0.39</td><td align="center" valign="middle" >0.18</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >CaO</td><td align="center" valign="middle" >0.61</td><td align="center" valign="middle" >−0.64</td><td align="center" valign="middle" >−0.43</td><td align="center" valign="middle" >0.90</td><td align="center" valign="middle" >−0.04</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Na<sub>2</sub>O</td><td align="center" valign="middle" >−0.41</td><td align="center" valign="middle" >0.55</td><td align="center" valign="middle" >0.31</td><td align="center" valign="middle" >−0.15</td><td align="center" valign="middle" >0.56</td><td align="center" valign="middle" >−0.20</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >K<sub>2</sub>O</td><td align="center" valign="middle" >−0.85</td><td align="center" valign="middle" >0.80</td><td align="center" valign="middle" >0.46</td><td align="center" valign="middle" >−0.66</td><td align="center" valign="middle" >0.28</td><td align="center" valign="middle" >−0.78</td><td align="center" valign="middle" >0.11</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >P<sub>2</sub>O<sub>5</sub></td><td align="center" valign="middle" >−0.18</td><td align="center" valign="middle" >0.09</td><td align="center" valign="middle" >0.41</td><td align="center" valign="middle" >−0.42</td><td align="center" valign="middle" >−0.52</td><td align="center" valign="middle" >−0.53</td><td align="center" valign="middle" >−0.33</td><td align="center" valign="middle" >0.38</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >B</td><td align="center" valign="middle" >−0.88</td><td align="center" valign="middle" >0.82</td><td align="center" valign="middle" >0.68</td><td align="center" valign="middle" >−0.39</td><td align="center" valign="middle" >0.36</td><td align="center" valign="middle" >−0.58</td><td align="center" valign="middle" >0.27</td><td align="center" valign="middle" >0.82</td><td align="center" valign="middle" >0.38</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Ba</td><td align="center" valign="middle" >−0.90</td><td align="center" valign="middle" >0.89</td><td align="center" valign="middle" >0.68</td><td align="center" valign="middle" >−0.67</td><td align="center" valign="middle" >0.33</td><td align="center" valign="middle" >−0.80</td><td align="center" valign="middle" >0.35</td><td align="center" valign="middle" >0.89</td><td align="center" valign="middle" >0.40</td><td align="center" valign="middle" >0.85</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Pb</td><td align="center" valign="middle" >−0.06</td><td align="center" valign="middle" >0.06</td><td align="center" valign="middle" >0.41</td><td align="center" valign="middle" >−0.27</td><td align="center" valign="middle" >−0.20</td><td align="center" valign="middle" >−0.14</td><td align="center" valign="middle" >0.24</td><td align="center" valign="middle" >−0.06</td><td align="center" valign="middle" >0.15</td><td align="center" valign="middle" >0.10</td><td align="center" valign="middle" >0.21</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Sr</td><td align="center" valign="middle" >−0.10</td><td align="center" valign="middle" >0.16</td><td align="center" valign="middle" >0.25</td><td align="center" valign="middle" >0.25</td><td align="center" valign="middle" >0.15</td><td align="center" valign="middle" >0.23</td><td align="center" valign="middle" >0.37</td><td align="center" valign="middle" >−0.09</td><td align="center" valign="middle" >0.00</td><td align="center" valign="middle" >0.26</td><td align="center" valign="middle" >0.12</td><td align="center" valign="middle" >0.44</td><td align="center" valign="middle" >1.00</td></tr></tbody></table></table-wrap><p>In the Irbiben deposit, variations in lead and strontium are not significant, indicating poor mobility of these elements during alteration.</p><p>v New MIA alteration index</p><p>This work led to the development of a new index of alteration MIA, resulting from the modification of that of Ishikawa, modified by substitution in the previous formula of sodium by total iron. It is calculated from the weight percentages of oxides and is obtained by the formula:</p><disp-formula id="scirp.80182-formula2"><graphic  xlink:href="//html.scirp.org/file/5-2170556x8.png"  xlink:type="simple"/></disp-formula><p>Its use has shown certain tendencies, notably an evolution of the inverse index to that of the SiO<sub>2</sub> grade in the samples (<xref ref-type="fig" rid="fig7">Figure 7</xref>).</p><p>The enrichment of iron and calcium is related to the preliminary observations: the development of hydrothermal calcite and newly formed chlorite when getting close to the the mineralized vein. Iron-bearing sulphides are also more abundant at this level, as shown by the metallographic study. From another angle, the variation of this index shows an increase in magnesium and potassium when getting away from the gold structure. This tendency shows the development of sericitization. On the other hand, chlorite in this case is rather magnesian. Differences have been detected both in the microscope and in the microprobe [<xref ref-type="bibr" rid="scirp.80182-ref3">3</xref>] .</p></sec><sec id="s5_3"><title>5.3. Discussion</title><p>The gold mineralization of Akka Tagragra inlier is carried by quartz veins and hosted by metasedimentary and igneous formations. Unlike the main deposit Iourirn in dykes of basic magmatic rocks [<xref ref-type="bibr" rid="scirp.80182-ref3">3</xref>] , no dyke was intersected by gold veins at Irbiben. However, as at Iourirn where hydrothermal alterations were noted by Zouhair [<xref ref-type="bibr" rid="scirp.80182-ref7">7</xref>] and Benbrahim [<xref ref-type="bibr" rid="scirp.80182-ref3">3</xref>] the hydrothermal phenomena were recorded in Irbiben. The placement of these veins has led to the formation of quartz with recrystallization texture, iron chorite, recognized by Benbrahim [<xref ref-type="bibr" rid="scirp.80182-ref3">3</xref>] and sericite. The newly formed calcite associated with quartz corresponds to what has already been described by Dub&#233; and Gosselin [<xref ref-type="bibr" rid="scirp.80182-ref12">12</xref>] . The interest of this study was to demonstrate the hydrothermalism accompanying the setting of inlier mineralization. Following the example of the Ishikawa alteration index, the new MIA index developed in this study will show enrichment in iron and calcium in placement of gold veins in similar deposits. However, it would be interesting to carry out a further mineralogical characterization of the hydrothermal minerals by microprobe. Moreover, a combined study of fluid inclusions in the host rocks to compare them to metasomatised rocks would better characterize the hydrothermal fluid.</p></sec></sec><sec id="s6"><title>6. Conclusions</title><p>The host formations of the Irbiben deposit are composed of rocks generally metamorphosed in the green schist facies. They are predominantly sandstone schists and metasandstone, to which are added metapelites, quartzites and grauwakes. A granitic massif south of the deposit and diorite dykes has been identified.</p><p>The hydrothermal activity has led to the formation of secondary minerals such as calcite, sericite, chlorite or quartz Q<sub>III</sub>. These mineralogical changes are reflected in the chemical composition of the rocks, resulting in a much higher silica and calcium grade, much more important in the hanging walls accompanied by an increase in iron. These tendencies could be corroborated by the use of the new MIA alteration index bringing out the iron enrichment accompanying the calcitization, as well as the matrix of correlations showing the mobility of certain elements such as calcium and barium, or still the very positive correlation between boron, potassium and iron. By moving away from the gold structure, the predominant ferromagnesian and alkaline grades are due to sericitization and chloritization but also and above all to a predisposition of the host, initially rich in these elements. Such changes noted in the hanging walls and the host rock of the Irbiben deposit reveal aquocarbon mineralization fluid of the orogenic deposits. The latter can influence the host rock by adding aqueous silica. Its CO<sub>2</sub> component associated with the Ca of host rocks causes the formation of hydrothermal calcite in the hanging walls. This explains the importance of silicification and calcitisation in the hanging walls.</p></sec><sec id="s7"><title>Cite this paper</title><p>Boya, T.K.L.-D., Houssou, N.N., Allialy, M.E., Gnanzou, A., Erraioui, L., Maamar, B. and M’Rabet, S. (2017) Hydrothermal Alterations in Irbiben Gold Deposit (Tagragra Akka, Western Anti-Atlas, Morocco): Petrographic and Geochemical Characterization. Journal of Geoscience and Environment Protection, 5, 46-60. https://doi.org/10.4236/gep.2017.511005</p></sec></body><back><ref-list><title>References</title><ref id="scirp.80182-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Brisson, H. (1998) Caractéristiques, chronologie et typologie des minéralisations aurifères de la région du lac Shortt (Québec), sous-province archéenne de l’Abitibi. [Characteristics, Chronology and Typology of Gold Mineralizations in the Shortt Lake Area (Quebec), Abitibi Archean Subprovince.] Thèse Université du Québec à Chicoutimi, 296 p.</mixed-citation></ref><ref id="scirp.80182-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Belkabir, A., Hubert, C. and Hoy, D.L. (2004) Gold Emplacement and Hydrothermal Alteration in Metabasic Rocks at the Mouska Mine, Bousquet District, Abitibi, Quebec, Canada. The Canadian Mineralogist, 42, 1079-1096. https://doi.org/10.2113/gscanmin.42.4.1079</mixed-citation></ref><ref id="scirp.80182-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Benbrahim, M. (2005) Gisement aurifère d’Iourirn (Tagragra d’Akka, Anti-Atlas Occidental, MAROC): Caractérisation pétrographique, géochimique paléocirculations fluides. [Iourirn Gold Deposit (Tagragrad’Akka, Western Anti-Atlas, Morocco): Petrographic and Geochemical Characterization, Fluid Paleocirculations.] Thèse Université Moulay Ismail Meknès, 240 p.</mixed-citation></ref><ref id="scirp.80182-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Zoheir, B.A. and Qaoud, N.N. (2008) Hydrothermal Alteration Geochemistry of the Betam Gold Deposit, South Eastern Desert, Egypt: Mass-Volume-Mineralogical Changes and Stable Isotope Systematics. Applied Earth Science, 117, 55-76.</mixed-citation></ref><ref id="scirp.80182-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Boya, T.K.L.-D., Mhaili, M., Bouabdli, A., Erraioui, L. and Mrabet, S. (2013) Signature pétrographique et géochimique de l’altération hydrothermale dans le gisement aurifère d’Ifarar (Tagragra d’Akka, Anti-Atlas occidental, Maroc). [Petrographic and Geochemical Signature of Hydrothermal Alteration in Ifarar Gold Bearing Deposit (Akka Tagragra, Western Anti-Atlas, Morocco).] ScienceLib Editions Mersenne, 5, Géologie, No. 130214.</mixed-citation></ref><ref id="scirp.80182-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Soulaimani, A. (1998) Interaction socle/couverture dans l’Atlas occidental (Maroc): Rifting fini-protérozoique et orogenèse hercynienne. [Basement/Cover Interaction in the Western Atlas (Morocco): Late Proterozoic Rifting and Hercynian Orogeny.] Thèse Université Cadi Ayyad Marrakech, 224 p.</mixed-citation></ref><ref id="scirp.80182-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Zouhair, M. (1992) Les paléocirculations fluides dans la Tagragra d’Akka (Anti-Atlas, Maroc). Etude combinée des inclusions fluides et de la déformation des quartz aurifères: Conséquence pour la métallogénie de l’or. [Fluid Paleocirculations in Akka Tagragra (Anti-Atlas, Morocco). Combined Study of Fluid Inclusions and the Deformation of Gold-Bearing Quartz: Consequence for the Metallogeny of Gold.] Thèse INPL, 384 p.</mixed-citation></ref><ref id="scirp.80182-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Mortaji, A. (1989) La boutonnière précambrienne de Tagragra d’Akka (anti-atlas occidental, Maroc): Pétrologie et géochimie des granitoides, filons basiques et métamorphites associées. [Precambrian Inlier of Akka Tagragra (Western Anti-Atlas, Morocco): Petrology and Geochemistry of Granitoids, Basic Veins and Associated Metamorphites.] Thèse de l’Université Henri Poincaré, Nancy 1, 211 p.</mixed-citation></ref><ref id="scirp.80182-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Phillips, G.N., Groves D.I. and Brown, I.J. (1987) Source Requirements for the Golden Mile Kalgoorli: Significance of the Metamorphic Replacement Model for Archean Gold Deposits. Canadian Journal of Earth Sciences, 24, 1643-1651. https://doi.org/10.1139/e87-158</mixed-citation></ref><ref id="scirp.80182-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Mikucki, E.J. and Ridley, J.R. (1993) The Hydrothermal Fluid of Archean Lode-Gold Deposits at Different Metamorphic Grades: Compositional Constraints from Ore and Wallrock Alteration Assemblages. Mineralium Deposita, 28, 469-481. https://doi.org/10.1007/BF02431603</mixed-citation></ref><ref id="scirp.80182-ref11"><label>11</label><mixed-citation publication-type="book" xlink:type="simple">Ridley, J.R. and Diamond, L.W. (2000) Fluid Chemistry of Orogenic Lode Gold Deposits and Implications for Genetic Models. In: Hagemann, S.G. and Brown, P.E., Eds., Gold in 2000, Society of Economic Geologists, Reviews in Economic Geology 13, 141-162.</mixed-citation></ref><ref id="scirp.80182-ref12"><label>12</label><mixed-citation publication-type="book" xlink:type="simple">Dubé, B. and Gosselin, P. (2007) Greenstone-Hosted Quartz-Carbonate Vein Deposits. In: Goodfellow, W.D., Ed., Mineral Deposits of Canada: A Synthesis of Major Deposit-Types, District Metallogeny, the Evolution of Geological Provinces, and Exploration Methods, Geological Association of Canada, Mineral Deposits Division, Special Publication 5, 49-73.</mixed-citation></ref></ref-list></back></article>