<?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.2020.104016</article-id><article-id pub-id-type="publisher-id">OJMS-103300</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>
 
 
  Intertidal Biodiversity and Their Response to Climatic Variables, Temperature and pH—What We Know
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>P.</surname><given-names>M. Mohan</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>V.</surname><given-names>Swathi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Ocean Studies and Marine Biology, Pondicherry University of Campus, Port Blair, Andaman and Nicobar 
Islands, India</addr-line></aff><pub-date pub-type="epub"><day>25</day><month>08</month><year>2020</year></pub-date><volume>10</volume><issue>04</issue><fpage>203</fpage><lpage>217</lpage><history><date date-type="received"><day>30,</day>	<month>May</month>	<year>2020</year></date><date date-type="rev-recd"><day>27,</day>	<month>September</month>	<year>2020</year>	</date><date date-type="accepted"><day>30,</day>	<month>September</month>	<year>2020</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>
 
 
  As per the Essential Climate Variables (ESV) of World Meterological Organisation (WMO), the physical, chemical and biological variables critically contribute to the earth’s climate. Among them, the variables such as temperature and pH in the marine environment may affect seriously and in turn it has an impact on the biota, especially in the intertidal environment, where it has brunt force. According to United Nations Framework Convention on Climate Change (UNFCCC), the datasets should provide the empirical evidence needed to predict the climate change and evoluate the mitigation and adaptation measures. Under this context, a review was carried out to know what extent marine scientists understand this factor and what level the biodiversity was evoluated and its impact was analysed in this article. Based on the existing literature review, it was understood that only a few groups that also only few species from these groups were studied in this aspect. The remaining groups and their species and their basic trophic were not evolved in this aspect. So, the marine scientific community, environmentalist and policy makers should take stock on this aspect and give thrust on this study.
 
</p></abstract><kwd-group><kwd>Climatic Variables</kwd><kwd> Temperature</kwd><kwd> pH</kwd><kwd> Salinity</kwd><kwd> Marine</kwd><kwd> Biodiversity</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Climatic change is one of the important factors to consider for the futuristic research activities, especially with biodiversity concern. According to Global Climate Observing System (GCOS), it should be ensured that observations and information needed to address the climate issues are obtained and made available to all potential users. The World Meterological Organisation (WMO) also suggested that under the Essential Climate Variables (ECV) the datasets on EVS should provide the empirical evidence, which needed to understand and predict the climatic change to evoluate the mitigation and adaptation measures to underpin the climatic services [<xref ref-type="bibr" rid="scirp.103300-ref1">1</xref>]. Under this programme, it was suggested generating and archiving data on the variables, wherever possible, using historical dataset. The predication of the future climate states that the temperature is the important factor for the terrestrial and temperature and pH are the two major components to be altered in the marine environment concern. As predicted by IPCC [<xref ref-type="bibr" rid="scirp.103300-ref2">2</xref>], a rise of temperature around 1˚C to 2.5˚C was suggested based on the year 2000 data. The expected outcome of this 20% - 30% of plants and animals may extinct and Island States undergo the sea due to increase of sea level rise. The climate change affected drastically and the ecosystem shifts and numerous extinctions will be resultant [<xref ref-type="bibr" rid="scirp.103300-ref3">3</xref>] - [<xref ref-type="bibr" rid="scirp.103300-ref8">8</xref>].</p><p>The effect of climate change is rapid and highly influence in marine ecosystem, especially in the intertidal zone where the upper temperature differences have their impact [<xref ref-type="bibr" rid="scirp.103300-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref12">12</xref>]. If the species cannot acclimatize physiologically or change genetically to cope with temperature increment to move cooler habitats, i.e. high latitude [<xref ref-type="bibr" rid="scirp.103300-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref17">17</xref>]. It was proposed that the shift of marine species in an average 19 km/year [<xref ref-type="bibr" rid="scirp.103300-ref11">11</xref>] than the terrestrial shift, i.e. 0.6 km/year [<xref ref-type="bibr" rid="scirp.103300-ref5">5</xref>]. Since, the shift range can be predicated well in marine species because of its thermal tolerance limit [<xref ref-type="bibr" rid="scirp.103300-ref18">18</xref>], so as the web interactions changes within ecological community [<xref ref-type="bibr" rid="scirp.103300-ref19">19</xref>].</p></sec><sec id="s2"><title>2. Methodology</title><p>Understanding the importance of impact of temperature and pH variables on the intertidal life forms, the existing literature was scanned. The available information was shared here to understand the level of our knowledge on this aspect and discussed the views for the future need on this aspect. Even though good amount of literature is available on the distribution and taxonomy, the impact of the individual group is species were scanty. The available studies were discussed in this article.</p></sec><sec id="s3"><title>3. Intertidal Region</title><p>The seashore which covered during the high tide and exposed during the low tide is defined as intertidal zone or littoral zone. This eco zone covers a unique biome with variety of plant and animal [<xref ref-type="bibr" rid="scirp.103300-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref21">21</xref>]. This zone is characterised by unique temperature, ecological factors and micro climates. This zone is divided into four distinct regions:</p><p>Lower Littoral Zone - Low Tide Zone</p><p>This area is closest to the sea and submerged majority time with seawater. The waves in this region protect the harmful radiation and severe temperature fluctuation. The species lives in this region are larger in size, greater in number, more diverse than the other areas of intertidal zone. The organisms in the low tide zone do not have to be well adapted to drying out and temperature extremes. The common fauna and flora observed in this region are sea anemone, brown sea weed, green algae, chiton, crabs, hydroids, isopods, limpets, mussels, sometimes small fishes.</p><p>Mid-Littoral Zone - Mid Tide Zone</p><p>The region is submerged half of the time of tidal fluctuations. The plant and animal species are living in this region but not as diver as Low Tide Zone. The organisms in the mid tidal zone are snails, sponges, sea stars, barnacles, mussels, sea palms and crabs.</p><p>Upper Mid-Littoral Zone - High Tide Zone</p><p>The zone is submerged during the high tide only. Very few plants and animals survived in this region. The most of the animals in this region are mobile (Crab) or attached to the substrate (Barnacles). The organisms in the high tidal zone are seaweeds, marine algae, sea anemone, starfish, chiton, crabs, mussels, nudibranchs and hermitcrabs.</p><p>Splash Zone</p><p>The splash zone is located above the upper mid-littoral zone. The water splash during the high tide by the wavers and never submerged with water.</p></sec><sec id="s4"><title>4. Results and Discussion</title><sec id="s4_1"><title>4.1. Temperature</title><p>All organisms have an influence on climatic variables in the range of molecular to ecosystem scales because the temperature dependent process is imminent [<xref ref-type="bibr" rid="scirp.103300-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref24">24</xref>]. Comparative to terrestrial species marine ectotherms act faster because of its sedentary nature and short life spans prevent escape from the change of environmental regimes [<xref ref-type="bibr" rid="scirp.103300-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref26">26</xref>]. The flora and fauna existed in the intertidal regime responding quicker than the higher trophic level [<xref ref-type="bibr" rid="scirp.103300-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref29">29</xref>], because this quicker response leads to surge of deficiency of food chain [<xref ref-type="bibr" rid="scirp.103300-ref30">30</xref>]. Even though, semidiurnal and diurnal tidal effect along with seasonal variable may affect the intertidal organism to the tune of 2.5˚C over a single tidal cycle [<xref ref-type="bibr" rid="scirp.103300-ref31">31</xref>], the temperature increment of air may affect further on this fact leads to some kind of thermal extremes for the intertidal flora and fauna.</p><p>The temperature increment affected the Boreal Barnacle Semibalanus balanoides larval development [<xref ref-type="bibr" rid="scirp.103300-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref33">33</xref>]. The blue mussel Mytilus edulis exhibited impaired respiration and metabolism change [<xref ref-type="bibr" rid="scirp.103300-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref36">36</xref>]. The pink coralline algae show impaired growth in the intertidal environment [<xref ref-type="bibr" rid="scirp.103300-ref37">37</xref>]. The Pacific Oyster Crassostrea gigas (<xref ref-type="fig" rid="fig1">Figure 1</xref>) located in the intertidal zone adapted to massive temperature fluctuations around 2˚C in a tidal cycle. Additionally, the exposure to high thermal variability can cause shifts in gene expression patterns which set limits for physiological function [<xref ref-type="bibr" rid="scirp.103300-ref38">38</xref>]. The sea star Crossaster papposus (<xref ref-type="fig" rid="fig2">Figure 2</xref>) has lecithotrophic larvae which have less susceptible to environmental change than the planktotrophic larvae of asteroid species.</p><p>The enhanced respiration rates of faunal community through temperature raise affect the carbon balance of macroalgae assemblages which declines net productivity of seaweed and due course of time species richness [<xref ref-type="bibr" rid="scirp.103300-ref39">39</xref>]. The crab has good sustainability for temperature and pH variation in the intertidal regions. However, the effect of these combined two factors leads to decline its resistivity and its population. This in turn exhibited a potential long term adverse effect on the ectotherm. The sea anemone Actinia equina (<xref ref-type="fig" rid="fig3">Figure 3</xref>) in the rocky Mediterranean coast exhibited the growth of polyp will shunted along with reduced biomass during the raise of temperature [<xref ref-type="bibr" rid="scirp.103300-ref40">40</xref>]. The brown dinoflagellates (Symbiodinium californium, A. T. Banaszak, R.Iglesias-Prieto &amp; R. K. Trench</p><p>and S. muscatinei, La Jeunesse &amp; R. K. Trench) called zooxanthellae translocate during the high temperature to the host [<xref ref-type="bibr" rid="scirp.103300-ref41">41</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref42">42</xref>].</p></sec><sec id="s4_2"><title>4.2. pH</title><p>The studies on the pH of marine water suggested that during the end of 21<sup>st</sup> Century, the CO<sub>2</sub> level may be increased to three to four fold than the pre-industrial levels [<xref ref-type="bibr" rid="scirp.103300-ref43">43</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref44">44</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref45">45</xref>]. This increment may effect on the surface of the water and increase the dissolved CO<sub>2</sub> and in turn alter the seawater pH which was not seen in the last 300 million years by the change the carbonate chemistry [<xref ref-type="bibr" rid="scirp.103300-ref46">46</xref>]. The year 2016, carbon dioxide parts in the atmosphere surpassed 400 ppm (parts per million), the highest since the Pliocene epoch, a geological period known for its warm temperatures. Morris and Taylor [<xref ref-type="bibr" rid="scirp.103300-ref47">47</xref>], Truchot [<xref ref-type="bibr" rid="scirp.103300-ref48">48</xref>] and Wootton et al., [<xref ref-type="bibr" rid="scirp.103300-ref49">49</xref>] reported that in the tide pool studies the pH changed from 9.5 to 6.5 which was higher than the proposed value of next century predication on the surface water. Feely et al., [<xref ref-type="bibr" rid="scirp.103300-ref45">45</xref>] and Hofmann et al., [<xref ref-type="bibr" rid="scirp.103300-ref50">50</xref>] reported that the intensity of upwelling increased and in turn the deep hypercarbanic waters mixing in the surface water also lowering the pH towards acidic side.</p><p>The change of pH was termed as Ocean Acidification (OA) as mentioned by Caldeira and Wickett [<xref ref-type="bibr" rid="scirp.103300-ref51">51</xref>] and Meehl et al., [<xref ref-type="bibr" rid="scirp.103300-ref44">44</xref>]. This large variation of pH may affect the biota’s metabolism, growth and reproduction [<xref ref-type="bibr" rid="scirp.103300-ref52">52</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref53">53</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref54">54</xref>] through the intracellular pH homeostasis [<xref ref-type="bibr" rid="scirp.103300-ref55">55</xref>]. This may lead to ecological implications by the way disappearance of the particular species or genetical modification of the same and in turn affect the local biodiversity with the result of disturbed community composition [<xref ref-type="bibr" rid="scirp.103300-ref55">55</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref56">56</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref57">57</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref58">58</xref>]. Further, the change of pH may be affected the intertidal regions of the ocean than the deeper habitats [<xref ref-type="bibr" rid="scirp.103300-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref50">50</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref59">59</xref>]. This fact is very much significant for the crustaceans and snails [<xref ref-type="bibr" rid="scirp.103300-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref60">60</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref61">61</xref>]. However, it was not affected the teleost fish and brachyuran crabs but increased its availability more [<xref ref-type="bibr" rid="scirp.103300-ref52">52</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref62">62</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref63">63</xref>]. Another interesting findings also observed that the early life history of organisms (embroyonic, larval or juvenile stages) show more response on the OA factor than the latter stages of their life history [<xref ref-type="bibr" rid="scirp.103300-ref54">54</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref64">64</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref65">65</xref>]. This factor was very much significant for mollusks, echinoderm and crustaceans [<xref ref-type="bibr" rid="scirp.103300-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref60">60</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref66">66</xref>] [<xref ref-type="bibr" rid="scirp.103300-ref67">67</xref>]. The studies on the porcelain crab Petrolishthes cinctipes stated (<xref ref-type="fig" rid="fig4">Figure 4</xref>) that the survival rate of juvenile reduced to the tune of 30% in hepercapnic waters influence [<xref ref-type="bibr" rid="scirp.103300-ref68">68</xref>]. The above studies were clearly mentioned that the whole life history of a fauna or flora should be studied [<xref ref-type="bibr" rid="scirp.103300-ref69">69</xref>] to understand the impact of OA in the marine environment. The California mussel—Mylitis californiansis (<xref ref-type="fig" rid="fig5">Figure 5</xref>) precipitated smaller shells with less thickness due to pH level towards acidic [<xref ref-type="bibr" rid="scirp.103300-ref70">70</xref>]. The coralline algae recruitment and deficient growth were observed under acidic conditions [<xref ref-type="bibr" rid="scirp.103300-ref71">71</xref>].</p><p>As reported by Alenius and Munguia [<xref ref-type="bibr" rid="scirp.103300-ref72">72</xref>] the species Paradella dianae (<xref ref-type="fig" rid="fig6">Figure 6</xref>) from the Isopod living in the intertidal regions showed its variation among the consumption of oxygen, swimming speed, food response varied when the pH conditions varies. As reported by Orr et al., [<xref ref-type="bibr" rid="scirp.103300-ref43">43</xref>] and Bednaršek et al., [<xref ref-type="bibr" rid="scirp.103300-ref73">73</xref>], the OA may also reduce calcification in planktonic organisms. The pH fluctuate daily ≥ 0.5 pH units and up to ≥1 pH level on temperate rocky shores [<xref ref-type="bibr" rid="scirp.103300-ref49">49</xref>]. The coral reef environment suggested that the pH varies ≥ 0.5 pH units day and night cycles Birkeland et al., [<xref ref-type="bibr" rid="scirp.103300-ref74">74</xref>].</p></sec></sec><sec id="s5"><title>5. Conclusion</title><p>The existing literature was stated that the studies on intertidal fauna and flora for the impact on climatic variables executed only for few groups of organisms. The number of other intertidal fauna like polycheate, sponges, hydroids, bryozoans, etc., (<xref ref-type="table" rid="table1">Table 1</xref>) is not known for its effect on the temperature and pH changes in the intertidal mechanism, which is highly essential for the food web of marine trophic as a total. If scientific community does not understand its effect, which in turn estimation of the range extension of faunal distribution will become more cumbersome and effect on the climatic variable will not be understood fully</p><table-wrap-group id="1"><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Intertidal faunal and floral distribution</title></caption><table-wrap id="1_1"><table><tbody><thead><tr><th align="center" valign="middle"  colspan="3"  >Intertidal Organisms</th></tr></thead><tr><td align="center" valign="middle" >Upper littoral zones</td><td align="center" valign="middle" >Mid littoral zones</td><td align="center" valign="middle" >Lower littoral zones</td></tr><tr><td align="center" valign="middle" >Periwinkles</td><td align="center" valign="middle" >Mussels</td><td align="center" valign="middle" >Hydrozoans</td></tr><tr><td align="center" valign="middle" >Littorina scabra</td><td align="center" valign="middle" >Mylitis californianus</td><td align="center" valign="middle" >Porpita porpita</td></tr><tr><td align="center" valign="middle" >Nerita atropurprea</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Physalia physalisa</td></tr><tr><td align="center" valign="middle" >Nerita articulata</td><td align="center" valign="middle" >Barnacles</td><td align="center" valign="middle" >Velella velella</td></tr><tr><td align="center" valign="middle" >Nerita Costata</td><td align="center" valign="middle" >Semibalanus balanoides</td><td align="center" valign="middle" >Obelia geniculata</td></tr><tr><td align="center" valign="middle" >LIttorina scutulata</td><td align="center" valign="middle" >Chthamalus malayanus</td><td align="center" valign="middle" >Aurelia aurita</td></tr><tr><td align="center" valign="middle" >Blue green algae</td><td align="center" valign="middle" >Lepas anatifera</td><td align="center" valign="middle" >Doto Sp</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Shrimps</td></tr><tr><td align="center" valign="middle" >Green algae</td><td align="center" valign="middle" >Chitons</td><td align="center" valign="middle" >Periclimenes brevicarpalis</td></tr></tbody></table></table-wrap><table-wrap id="1_2"><table><tbody><thead><tr><th align="center" valign="middle" >Enteromorpha</th><th align="center" valign="middle" >Ischnochiton dispar</th><th align="center" valign="middle" >Sea anemone</th></tr></thead><tr><td align="center" valign="middle" >Calerpa</td><td align="center" valign="middle" >Stenoplax limaciformis</td><td align="center" valign="middle" >Stoichatis Sp</td></tr><tr><td align="center" valign="middle" >Padina</td><td align="center" valign="middle" >Chiton stokesii</td><td align="center" valign="middle" >Anthopleura elaegantissima</td></tr><tr><td align="center" valign="middle" >Brown algae</td><td align="center" valign="middle" >Acanthochitona hirudiniformis</td><td align="center" valign="middle" >Anthopleura anathogrammica</td></tr><tr><td align="center" valign="middle" >Halymenia Sp</td><td align="center" valign="middle" >Acanthochitona ferreirai</td><td align="center" valign="middle" >Dardamus Sp</td></tr><tr><td align="center" valign="middle" >Halimeda Sp</td><td align="center" valign="middle" >Chaetopleura lurida</td><td align="center" valign="middle" >Stichodactyla haddoni</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >lepidachitona beanie</td><td align="center" valign="middle" >Sponges</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Callistoplax retusa</td><td align="center" valign="middle" >Oceanapia saggitaria</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Callisstochiton expressus</td><td align="center" valign="middle" >Neopetrosia sp.</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Flat Worms</td><td align="center" valign="middle" >Haliclona sp.</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Pseudoceros coralliophilus</td><td align="center" valign="middle" >Ircinia fusca</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Thysanozoon sp</td><td align="center" valign="middle" >Cinachyra Arabica</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Dysidea fragilis</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Limpets</td><td align="center" valign="middle" >Phyllospsongia calciformis</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Acmaea stellaris</td><td align="center" valign="middle" >Chondrilla australiensis</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Bryozoans</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Polychaetes</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Sea weeds</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Electra indica</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Sipunculids</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Crabs</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Oyster</td><td align="center" valign="middle" >Thalamita Sp</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Saccostrea cucullata</td><td align="center" valign="middle" >Ochypoda Sp</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Sesarma longipes</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Clam</td><td align="center" valign="middle" >Clibanarius Sp.</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Tridacna crocea</td><td align="center" valign="middle" >Uca anulips</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Uca vocans</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Uca marionis</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Paguras Sp</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Cancer magister</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Hemigrapsus nudus</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Oregonia gracilis</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Cardiopoma carnifex</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Limpets</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Acmaea stellaris</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Barnacles</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Balanus glandula</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Semibalanus cariocus</td></tr></tbody></table></table-wrap><table-wrap id="1_3"><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th><th align="center" valign="middle" >Polliapes polymeras</th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Mussels</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Mylitis californianus</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Sea urchins</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Echinothrix calamaris</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Diadema stosum</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Stongylocentrotus purpuratus</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Isopod</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Isotea wosnesenki</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Sea Star</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Pisaster ochraeus</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Linkia Leavigata</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Culcita novaquinea</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Asterias Rubens</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Oyster</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Saccostrea cucullata</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Sea Cucumber</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Holothuria sp</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Zooplankton</td></tr></tbody></table></table-wrap></table-wrap-group><p>for the intertidal biodiversity. Not only that, the need to understand the impact of climatic variable to the fauna and flola of the intertidal regions as needed for Globla Climatic Observation System and if the scientist, not able to provide a clear cut information, the mitigation efforts was also not successful for future developmental aspects.</p></sec><sec id="s6"><title>Acknowledgements</title><p>I thank the Authorities of Pondicherry University for providing the facilities to execute this work in their Port Blair Centre. I also acknowledge the Indian Institute of Tropical Meteorology (IITM), Pune, under the Ministry of Earth Sciences for providing fund through Metflux Project.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s8"><title>Cite this paper</title><p>Mohan, P.M. and Swathi, V. (2020) Intertidal Biodiversity and Their Response to Climatic Variables, Temperature and pH—What We Know. 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