<?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">JGIS</journal-id><journal-title-group><journal-title>Journal of Geographic Information System</journal-title></journal-title-group><issn pub-type="epub">2151-1950</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jgis.2016.84036</article-id><article-id pub-id-type="publisher-id">JGIS-69059</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>
 
 
  Phytogenic Mounds (Nebkhas): Effect of &lt;i&gt;Tricomaria usillo&lt;/i&gt; on Sand Entrapment in Central-West of Argentina
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Graciela</surname><given-names>Pastrán</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>Eduardo</surname><given-names>Martínez Carretero</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Geobotánica y Ecología Vegetal, Departamento Biología-Museo de Ciencias Naturales, Facultad de Ciencias Exactas Físicas y Naturales, Universidad Nacional de San Juan, San Juan, Argentina</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>mgpastran@hotmail.com(GP)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>26</day><month>07</month><year>2016</year></pub-date><volume>08</volume><issue>04</issue><fpage>429</fpage><lpage>437</lpage><history><date date-type="received"><day>9</day>	<month>June</month>	<year>2016</year></date><date date-type="rev-recd"><day>accepted</day>	<month>23</month>	<year>July</year>	</date><date date-type="accepted"><day>26</day>	<month>July</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Nebkhas, developed by the trapping of sand within the body of a plant, were studied in the M&#233;danos Grandes system, arid central Argentina, during the springs of 2009-2010. The dynamics of nebkhas was studied in three draas (megadunes), and considering both orientations: leeward and windward. The Drift Potential (DP) for the study area was 42, evidencing the inactivity of the sand dunes or the scarce activity only in crests. Dominant sand movement is in south-southeast direction, with deflation processes at the southern side of the nebkhas. All nebkhas showed uniformity in the morphometry. 
  Tricomaria usillo
   is the dominant plant species in the nebkha formation process; and results showed a significant positive relationship between nebkha and canopy volumes.
 
</p></abstract><kwd-group><kwd>Sand Dunes</kwd><kwd> Nebkhas</kwd><kwd> Dynamics</kwd><kwd> Vegetation</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Psammophilous systems occur both in oceanic and continental regions; in these last, they occupy arid environments characterized by wide temperature range, scarce rainfall and high annual water deficit.</p><p>These systems encompass wide areas covered with aeolian sands where wind plays a determining role in landscape structure and in plant species distribution, principally due to its desiccant physiological effect and the mechanical action of burial and uncovering of plants ( [<xref ref-type="bibr" rid="scirp.69059-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.69059-ref2">2</xref>] ).</p><p>The effect of wind on sand dunes is different between exposures, with the windward slope being subjected to maximal erosion. Wind velocity increases toward the crest; on the lee slope, by expansion of flux, wind and its transport capacity diminish ( [<xref ref-type="bibr" rid="scirp.69059-ref3">3</xref>] ). This change induced by the topography of sand dunes will influence sand transport ( [<xref ref-type="bibr" rid="scirp.69059-ref4">4</xref>] ) and, consequently, vegetation composition ( [<xref ref-type="bibr" rid="scirp.69059-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.69059-ref9">9</xref>] ).</p><p>Vegetation obstructs the action of wind by retaining particles, functioning as sand traps ( [<xref ref-type="bibr" rid="scirp.69059-ref10">10</xref>] - [<xref ref-type="bibr" rid="scirp.69059-ref12">12</xref>] ), and generating mounds known as nebkhas. Nebkhas are normally fully developed on the crest of dunes where sand transport is maximal. Nebkhas are considered to be a type of phytogenic sand dunes that show different stages of development ( [<xref ref-type="bibr" rid="scirp.69059-ref13">13</xref>] ). Their morphology, similar to sand dunes, has direct relation with erosion-deposition processes due to wind acting differentially on each geotope, and it is controlled by growth patterns of shrub that retain the sand ( [<xref ref-type="bibr" rid="scirp.69059-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.69059-ref14">14</xref>] - [<xref ref-type="bibr" rid="scirp.69059-ref17">17</xref>] ). According to [<xref ref-type="bibr" rid="scirp.69059-ref18">18</xref>] , nehbka dunes typically are formed through ecogeomorphic feedbacks controlled by the interactions between vegetation growth and aeolian sedimentations.</p><p>In coincidence with [<xref ref-type="bibr" rid="scirp.69059-ref17">17</xref>] , three development stages can be recognized in nebkhas: fixation of aeolian sands by a shrub, growth of nebkhas and shrubs, erosion of nebkhas and degeneration of shrubs.</p><p>Nebkhas are dynamic elements of the geomorphology of sandy environments and play a relevant role in the ecological system, thus constituting habitats for smaller fauna (Rodentia, Iguanidae).</p><p>Environments with nebkhas are interesting cases where vegetation and aeolian transport are coupled; and where occurs highly heterogeneous distribution of perennial biomass, with little or no perennial plant species between nebkhas. This allows high rates of horizontal aeolian transport in nebkhas that may be part of a positive feedback in which increased aeolian transport leads to increased sediment transport from interspaces to nebkhas ( [<xref ref-type="bibr" rid="scirp.69059-ref19">19</xref>] ).</p><p>The nebkhas have been studied and described in Africa ( [<xref ref-type="bibr" rid="scirp.69059-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.69059-ref20">20</xref>] ), northern China ( [<xref ref-type="bibr" rid="scirp.69059-ref21">21</xref>] , Israel ( [<xref ref-type="bibr" rid="scirp.69059-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.69059-ref22">22</xref>] ), Spain ( [<xref ref-type="bibr" rid="scirp.69059-ref23">23</xref>] ), New Mexico [<xref ref-type="bibr" rid="scirp.69059-ref24">24</xref>] ), and the arid zone of Argentina ( [<xref ref-type="bibr" rid="scirp.69059-ref25">25</xref>] - [<xref ref-type="bibr" rid="scirp.69059-ref28">28</xref>] ), as common geomorphological-bio- logical components of psammophilous environments. They have been indicated on crests of linear semi-fixed dunes [<xref ref-type="bibr" rid="scirp.69059-ref29">29</xref>] and in inter-dune valleys [<xref ref-type="bibr" rid="scirp.69059-ref30">30</xref>] .</p><p>The structure and formation processes of nebkhas have been studied and discussed for different environments [<xref ref-type="bibr" rid="scirp.69059-ref31">31</xref>] - [<xref ref-type="bibr" rid="scirp.69059-ref34">34</xref>] . Authors as [<xref ref-type="bibr" rid="scirp.69059-ref35">35</xref>] suggested, as a simplification, to associate nebkha formation processes with soil degradation. Others as [<xref ref-type="bibr" rid="scirp.69059-ref28">28</xref>] did not find any chemical difference between soils of nebkhas and the surrounding soils, all nebkhas fixed by no leguminous species, and suggested only the mechanical effect of sand-holding shrubs: first as a barrier and later, as well, with their adventitious roots. In addition, the accumulation characteristics of nebkhas, which have developed extensively in these regions, can be used as a method of reconstructing environmental changes [<xref ref-type="bibr" rid="scirp.69059-ref36">36</xref>] .</p><p>The composition of nebkhas varies according to where they are formed: in flat areas they contain less than 50% of sand with dominance of loam and clay [<xref ref-type="bibr" rid="scirp.69059-ref21">21</xref>] ; while those in inter-dune valleys contain more than 90% of sand [<xref ref-type="bibr" rid="scirp.69059-ref37">37</xref>] . However, nebkhas in psammophilous environments such as on sand dunes are a different type [<xref ref-type="bibr" rid="scirp.69059-ref38">38</xref>] .</p><p>The nebkhas-vegetation relation has been studied by [<xref ref-type="bibr" rid="scirp.69059-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.69059-ref39">39</xref>] - [<xref ref-type="bibr" rid="scirp.69059-ref41">41</xref>] , among others, and concluded that there is a strong relationship between nebkha morphometry and plant morphology, and the heterogeneity in morphometry is due to differences in plant species cover.</p><p>The region of M&#233;danos Grandes has been studied in its geomorphological ( [<xref ref-type="bibr" rid="scirp.69059-ref42">42</xref>] - [<xref ref-type="bibr" rid="scirp.69059-ref44">44</xref>] and mineralogical aspects ( [<xref ref-type="bibr" rid="scirp.69059-ref45">45</xref>] ). According to [<xref ref-type="bibr" rid="scirp.69059-ref45">45</xref>] , these sand dunes are composed of lithic fragments (vulcanite, micaceous schist, amphibolites, mylonites, chert, sedimentary and calcite clasts) together with moderate percentages of feldspar with little presence of quartz, that correlate with the Pampean Aeolian Sand Sea and the climatic states suggested by [<xref ref-type="bibr" rid="scirp.69059-ref46">46</xref>] for a period of approximately 77,000 years. [<xref ref-type="bibr" rid="scirp.69059-ref47">47</xref>] indicates for the NW of the area sands with OSL (luminescence optically stimulated) ages of 600 &#177; 40 and 410 &#177; 40 years old, and for the N area OSL ages of 4300 &#177; 500 years at the bottom and of 4090 &#177; 335 years in the middle of the deposits. [<xref ref-type="bibr" rid="scirp.69059-ref42">42</xref>] differentiates, at 1:100,000 scale, by size, shape and orientation, two depositional formations: draas (mega sand dunes) and dunes. The area is formed by a complex pattern of dunes [<xref ref-type="bibr" rid="scirp.69059-ref48">48</xref>] . In the study area domain mega-barchan dunes with vegetated linear dunes superimposed.</p><p>In this paper we seek to analyze the dynamics of nebkhas in relation to wind, the intensity of sand movement, and associated shrubs in the continental dune system in the south-southeast of San Juan province.</p></sec><sec id="s2"><title>2. Material and Methods</title><sec id="s2_1"><title>2.1. Study Area</title><p>M&#233;danos Grandes is a static erg located in the south-southeast of San Juan province, Argentina, between 31˚40'S - 67˚42'W and 32˚00'S - 68˚10'W (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Sand dune height and the few or no possibilities of access constitute a barrier for field work.</p><p>The area is part of the South American Arid Diagonal [<xref ref-type="bibr" rid="scirp.69059-ref49">49</xref>] and the Minimum Mean Rainfall Axis of the Vinchina-Bermejo Depression with a mean temperature of 8.4˚C in the coldest month and 25.9˚C in the hottest [<xref ref-type="bibr" rid="scirp.69059-ref50">50</xref>] , and rainfalls lower than 150 mm/year. Annual water deficit is approximately 1168 mm [<xref ref-type="bibr" rid="scirp.69059-ref51">51</xref>] . The period with highest frequency of winds, and the driest one, is spring [<xref ref-type="bibr" rid="scirp.69059-ref52">52</xref>] .</p><p>Psammophytic vegetation includes shrubs and grasses, and it is dominated by P. urvilleanum Kunth on active and semi-fixed crests, accompanied by Aristida mendocina Phil., Neobouteloua lophostachya (Griseb.) Gould., among other herb species, with a cover of between 5% - 35%, and by thicket steppe in inter-sand dunes with Tricomaria usillo Hook. &amp; Arn.―Bulnesia retama (Gillies ex Hook. &amp; Arn.) Griseb community with low presence of Larrea divaricata Cav., Bougainvillea spinosa (Cav.) Heimerl., Junellia aspera (Gillies &amp; Hook.) Moldenke, Prosopis flexuosa DC, Cercidium praecox (Ruiz &amp; Pav. ex Hook.) Harms, Prosopidastrum globosum (Gill. ex Hook. &amp; Arn.) Burk, Ephedra boelckei Roig, etc. with 65% plant cover [<xref ref-type="bibr" rid="scirp.69059-ref53">53</xref>] . T. usillo, common in nebkhas, is a shrubby species up to 1.8 m tall and 1.5 m in canopy diameter, normally with 1 or 2 intensively branched stems.</p><p>Incursions of off-road vehicles are the only current human pressure, but drivers normally travel the same tracks; in addition, no historic use was recorded.</p><p>The dynamics of nebkhas was studied in three draas, considering both orientations: leeward and windward.</p></sec><sec id="s2_2"><title>2.2. Field Works</title><p>We randomly chose 30 nebkhas in total, 15 on the windward slope and 15 on the lee slope of the mega-barchan dunes, in a 1000 m long transect. All studied nebkhas were located on the middle of slopes of mega-dunes, and were randomly chosen with the consideration that they were completely isolated from neighboring nebkhas to avoid the internebkha effects. There are no nebkhas on dune crests. The difficulty of access to the area and the relatively low number of nebkhas allowed us to work only with this sample size.</p><p>On each selected nebkha, we inserted 1 mm graduated erosion pins, 20 cm height and 4 mm in diameter, on the north, south, east and west edges, and at the top. At each of these sites we used 3 pins separated by 20 cm, just enough to avoid interferences between them. Height variations (erosion-deposition) were recorded on each pin every fifteen days during the spring of 2009 (September-December). In addition, in each nebkha, we recorded maximum height and maximum (L) and minimum (l) length (along two perpendicular horizontal axes) to calculate volume and relationship between L/l and height.</p><p>The dominant plant species in nebkhas is Tricomaria usillo (Malpighiaceae). In all nebkhas, we dendrochronologically determined the age of T. usillo to estimate the time of nebkha formation. Stem diameter at plant neck height was recorded with metric tape and the relation between stem diameter-plant age was statistically determined.</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Study area in the south-southeast of San Juan province, Argentina</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-8401624x7.png"/></fig></sec></sec><sec id="s3"><title>3. Results and discussion</title><sec id="s3_1"><title>3.1. Nebkha Dynamics</title><p>According to the climate data obtained from the Las Chacritas Weather station (unpublished), located 15 km to the north and out of the study area, the highest frequency of winds with velocities over 22 km/hour (critical velocity for sand movement) (<xref ref-type="fig" rid="fig2">Figure 2</xref>), occurs in the spring period with south-east, east and south being the dominant wind directions.</p><p>Considering the Drift Potential (DP), usually used by aeolian geomorphologists ( [<xref ref-type="bibr" rid="scirp.69059-ref54">54</xref>] [<xref ref-type="bibr" rid="scirp.69059-ref55">55</xref>] ), given by: DP = (U<sup>2</sup> (U-U<sub>t</sub>/100*t)) (where U = wind speed in knots, U<sub>t</sub> = 12 knots, t: time when wind blew above the threshold velocity―17%), value for M&#233;danos Grandes system is 42. Obtained value highlights the inactivity of sand dunes or their scarce activity only on crests.</p><p>The mean variation in sand erosion-deposition was recorded from height variations on pins (mean of the three pins), in the nebkhas on all three mega-dunes, taking into account exposure and orientation, and for the 30 nebkhas randomly chosen, is shown in <xref ref-type="fig" rid="fig3">Figure 3</xref> and <xref ref-type="fig" rid="fig4">Figure 4</xref>, where negative values indicate deflation.</p><p>Mean variation in sand movement per exposure and orientation was, on windward slopes: 0.79 cm north, −0.02 cm east, −1.46 cm south and 0.13 cm west, on lee slopes: 0.59 cm north, 0.48 cm east, −0.45 cm south and 0.67 cm west.</p><p>The windward slope and south orientation of mega dunes show major sand movements by erosion. The deflation process occurred in the southern side and the deposition process in the northern side of the nebkhas. Lee nebkhas show low aeolian intensity and sand erosion/deposition was more uniformly distributed in all orientations. Erosion dominates on the windward slope, where it reaches its higher values (1.48 cm). In both exposures the south orientation shows erosion processes, coincident with the dominant wind direction. Considering all orientations the major sand accumulation occurred on the lee slope, reaching 1.74 cm in total; whereas on the windward slope it only reached 0.92 cm. The lowest sand deposition rate on the windward was recorded for the west orientation (0.13 cm) and the highest deposition rate in the north orientation (0.79 cm). On lee slopes, the lowest deposition was in the east orientation (0.48 cm) and the highest in the west (0.67 cm). All this would indicate that nebkhas grow through retention of sand eroded mostly from the south orientation. Lee nebkhas continue to grow whereas those on windward slopes are, in general, at the stage of erosion; [<xref ref-type="bibr" rid="scirp.69059-ref13">13</xref>] found similar results for coastal sand dunes of Ashdod (Israel).</p><p>The greatest sand movement, but with no significant differences, occurs on the windward slope, consistently with the studies by [<xref ref-type="bibr" rid="scirp.69059-ref56">56</xref>] and [<xref ref-type="bibr" rid="scirp.69059-ref57">57</xref>] .</p><p>Considering the results of ANOVA test and post hoc LSD (Least Significant Difference) test [<xref ref-type="bibr" rid="scirp.69059-ref58">58</xref>] , no statistical differences were found between exposures (p = 0.18) or orientations (p = 0.38) for erosion values, depositions and erosion/deposition rates, due to the high variation in the data.</p><p>Contrary to findings for other sand dune systems where crests showed the highest deposition rate and statistical differences between exposures [<xref ref-type="bibr" rid="scirp.69059-ref13">13</xref>] , in the M&#233;danos Grandes system erosion dominates on crests, and no nebkhas occur because the only species to grow is Panicum urvilleanum Kunth (Poaceae), a herb plant whose cover is lower than 5%, this difference possibly is due to of two different types of dunes in Israel and in San Juan.</p><p>According to [<xref ref-type="bibr" rid="scirp.69059-ref57">57</xref>] , variations in sand movement on taluses are primarily due to plant cover; in our study case,</p><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Wind frequencies (in percentage) with velocities over 22 km/hour</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-8401624x8.png"/></fig><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Sand erosion/deposition in windward nebkhas</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-8401624x9.png"/></fig><p>in both exposures, plant cover varied between 20% - 40%, which would explain the non-significant differences found in the mean rate of constant sand accumulation between both exposures. On the other hand, the floristic homogeneity found in our case can be related to their being fixed sand dunes with similar plant cover and floristic composition. Overall, a shrubland with 20% - 40% cover is dominant, where T. usillo is accompanied by Junellia aspera, Cercidium praecox, Larrea divaricata, Prosopidastrum globosum, Bulnesia retama and Ephe- dra boelckei.</p><p>No differences in sand movement or floristic composition were found between exposures in the M&#233;danos Grandes plant-fixed sand dune system, whilst strong correlations between plant community distribution and topography were found in coastal sand dunes with intense sand movement [<xref ref-type="bibr" rid="scirp.69059-ref5">5</xref>] .</p></sec><sec id="s3_2"><title>3.2. Nebkha-Shrub Relationship</title><p>Nebkhas vary in shape and size [<xref ref-type="bibr" rid="scirp.69059-ref24">24</xref>] , however those studied in M&#233;danos Grandes were homogenous with their</p><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Sand erosion/deposition in lee nebkhas</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-8401624x10.png"/></fig><p>mean height being respectively 0.62 &#177; 0.24 cm and 0.51 &#177; 0.20 cm on windward and lee slope, and their largest diameters being 4.71 &#177; 1.5 m and 4.25 &#177; 1.3 m, respectively. The relationship between L/l rate and height shows a correlation coefficient of r<sup>2</sup> = 0.84 (p &lt; 0.01) at 95% confidence level, with height being a good estimator of the L/l relationship and thus of the size of the nebkha. The resulting equation was L/l = 0.94 + 0.74*height. Similar results were found by [<xref ref-type="bibr" rid="scirp.69059-ref20">20</xref>] in nebkhas of Burkina Faso. On the other hand, data show uniformity in the morphometry of all nebkhas.</p><p>The shrub always present in nebkhas was Tricomaria usillo and, in some cases accompanied by Junellia aspera (in 3 nebkhas), Bulnesia retama (in 2), Bougainvillea spinosa (in 2), Prosopis flexuosa (in 1).</p><p>For all nebkhas, the stem diameter at plant neck height was recorded and the age of T. usillo was dendrochronologically determined. The stem diameter varied between 2.50 and 4.50 cm and the age of plants between 45 - 55 years old. The statiscal relationship obtained between stem diameter and age was: age = 35.515 + (2.5956*diam.) (n = 30; α = 0.05; r<sup>2</sup> = 0.54).</p><p>Taking into account nebkhas of different volumes and the age of T. usillo, estimated from diameters, the mean rate of constant sand accumulation for each geotope was estimated as being 0.140 m<sup>3</sup>/year and 0.155 m<sup>3</sup>/year for windward and lee slope respectively. The constant rate of growth in height was estimated as being 0.02 cm/year and 0.04 cm/year, for windward and lee slope, similar to estimate by [<xref ref-type="bibr" rid="scirp.69059-ref59">59</xref>] for nebkhas with Ephedra ochreata (0.02 cm/year) and with Larrea divaricata (0.03 cm/year) in the south of Mendoza province.</p><p>The mean dimensions of T. usillo canopies in the study area were: in windward, 137 cm in height, 107 cm in diameter and 0.45 m<sup>3</sup> in volume, and in lee slope, 135 cm in height, 113 cm in diameter and 0.48 m<sup>3</sup> in volume. Linear regression analysis showed a significant positive relationship between nebkha volume and canopy volume (α = 0.1, winward: r<sup>2</sup> = 0.88, lee slope: r<sup>2</sup> = 0.75), results that agree with those of [<xref ref-type="bibr" rid="scirp.69059-ref60">60</xref>] who found the same relation with Caragana tibetica in arid lands of Mongolia.</p></sec></sec><sec id="s4"><title>4. Conclusion</title><p>The M&#233;danos Grandes psammophilous system belongs to a low aeolian energy environment; in addition, it is stabilized by vegetation and shows no significant differences in sand movement between windward and lee slope. Consequently, the mean constant rate of sand accumulation is low. However, predominant winds from the south-southeast determine erosion on the windward slope and deposition on the lee slope, and therefore nebkhas superimposed on draas would indicate slow growth on the lee slope and moderate deterioration on the windward slope. In conclusion, nebkhas in this psammophilous environment were formed primarily by aeolian processes. In addition, this study indicates that T. usillo has significant effects on sand entrapment and in nebkha formation. Nebkhas are certainly a reliable indicator of sand dune dynamics, even in stable systems, such as the one studied here, where no vegetation or soil degradation processes were found to be related to this dynamics. Nebkhas that had been on lee slope now occurs on the windward and in erosion phase.</p></sec><sec id="s5"><title>Acknowledgements</title><p>To Dr. Tsoar (Department of Geography and Environmental Development, Ben-Gurion University of the Negev, Israel) for his valuable comments and suggestions, and to N. Horak (IADIZA) for assisting with the English language of the text.</p></sec><sec id="s6"><title>Funding</title><p>Project supported by CONICET and University National of San Juan Project E 726.</p></sec><sec id="s7"><title>Cite this paper</title><p>Graciela Pastr&#225;n,Eduardo Mart&#237;nez Carretero,1 1, (2016) Phytogenic Mounds (Nebkhas): Effect of Tricomaria usillo on Sand Entrapment in Central-West of Argentina. Journal of Geographic Information System,08,429-437. doi: 10.4236/jgis.2016.84036</p></sec><sec id="s8"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.69059-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Braun-Blanquet, J. (1979) Fitosociología. Bases para el estudio de las comunidades vegetales. Blume, Espana, 820 p.</mixed-citation></ref><ref id="scirp.69059-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Ennos, A. (1997) Wind as an Ecological Factor. 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