<?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">AJPS</journal-id><journal-title-group><journal-title>American Journal of Plant Sciences</journal-title></journal-title-group><issn pub-type="epub">2158-2742</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ajps.2015.68130</article-id><article-id pub-id-type="publisher-id">AJPS-56743</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Assisted Revegetation Following Contaminated Site Remediation in the Arctic: Four-Year Case Study of a Former Radar Site
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>arah</surname><given-names>Ficko</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>Brandon</surname><given-names>Smith</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>Barbara</surname><given-names>Zeeb</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Chemistry and Chemical Engineering, Royal Military College of Canada, Kingston, Canada</addr-line></aff><aff id="aff1"><addr-line>Present Address: 821 General Services Building, Department of Renewable Resources, University of Alberta, Edmonton, Canada</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>zeeb-b@rmc.ca(BZ)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>08</day><month>05</month><year>2015</year></pub-date><volume>06</volume><issue>08</issue><fpage>1301</fpage><lpage>1312</lpage><history><date date-type="received"><day>31</day>	<month>March</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>25</month>	<year>May</year>	</date><date date-type="accepted"><day>28</day>	<month>May</month>	<year>2015</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>
 
 
  Cape Dyer (DYE-M), located on the easternmost point of Baffin Island, is a former DEW line radar station built in 1956-57 which was upgraded in 1993 as part of the current North Warning System. Environmental studies in the late 1990s and early 2000s determined that extensive soil contamination existed across the site, and excavation of six landfills and subsequent reshaping of the area in 2008 disturbed approximately 19,700 m2. A four-year pilot project was conducted between 2009 and 2012 to investigate feasibility of, and determine methods to, accelerate revegetation of the disturbed area through assisted seed dispersal of native and non native species and selective transplantation of slow-growing shrub species. Prior to revegetation efforts, plant surveys conducted in July 2009 determined that 15 species were present in the undisturbed areas, of which 
  
  Salix arctica (~11%), 
  
  Vaccinium uliginosum L. (~8%), and 
  
  Empetrum nigrum L. (~5%) were the predominant species. A total of 14 species (three new) were observed growing on the disturbed areas between 2010 and 2012. The majority of 
  
  Lolium multiflorum (annual ryegrass) seeds planted as a nurse species in 2009 grew in 2010, but most were stunted and only observed in furrows or sheltered areas at a low density. 
  
  Salix arctica Pall. (willow) cuttings planted in “islands” of 20-30 cuttings in fall 2009 had a three-year survival rate of 82%, while a second set of cuttings planted in fall 2011 had a one-year survival rate of 93%. Visual observations indicate that patches of new vegetation are becoming more predominant on the disturbed area, especially around the willow islands, indicating the importance of microtopography for successful reclamation in arctic environments. Monitoring over ten or more years will be required to determine the long term success of this project.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Salix arctica&lt;/i&gt;</kwd><kwd> Revegetation</kwd><kwd> Disturbed Lands</kwd><kwd> Arctic</kwd><kwd> DEW Line</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Increased human activity and development in northern Canada and other polar environments have accelerated the disturbance of vast tracts of land in an already fragile ecosystem. During the 1950s, 42 Distant Early Warning (DEW) line radar stations were built along the 70˚ latitude, and linked with stations in the Polevault line to act as an early detection system for approaching hostile aircraft during the Cold War. Construction, operation and maintenance of these sites resulted in extensive contamination of soils and ground water at numerous locations across the Canadian arctic and subarctic [<xref ref-type="bibr" rid="scirp.56743-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref2">2</xref>] . The Cape Dyer DEW Line station, DYE-M (66˚40'N, 61˚21'W) was built in 1956-7 on the easternmost point of Baffin Island, on the Cumberland Peninsula bordering the Davis Strait, to link the DEW Line, Polevaultline, and Greenland communication facilities. The site accommodated several hundred personnel within the upper (radar) and lower (logistical) areas of the site, while equipment brought to site by water was loaded and offloaded at the beach (<xref ref-type="fig" rid="fig1">Figure 1</xref>). DYE-M was upgraded to an unmanned radar station as part of the new North Warning System in 1993.</p><p>Environmental studies conducted at DYE-M between 1997 and 2001 demonstrated that contaminated soils posed a potential risk to the arctic ecosystem [<xref ref-type="bibr" rid="scirp.56743-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref4">4</xref>] . Remediation work was initiated in 2005 at DYE-M, and completed in 2013. In 2008, extensive remediation work was conducted at the DYE-M beach to remove material from six buried landfills. Subsequent reshaping of the terrain resulted in approximately 19,700 m<sup>2</sup>of land completely or partially cleared of vegetation cover, leaving these areas unstable, more vulnerable to wind and water erosion, unable to provide food or habitats for animals, and visually unappealing.</p><p>In arctic environments, plant growth is constrained by short growing seasons, harsh environmental conditions (e.g., low temperature and rainfall), low species diversity (~1000 species) and minimal soil fertility [<xref ref-type="bibr" rid="scirp.56743-ref5">5</xref>] -[<xref ref-type="bibr" rid="scirp.56743-ref7">7</xref>] . Following disturbance or creation of new habitat, plant communities develop and change over time through a series of succession processes [<xref ref-type="bibr" rid="scirp.56743-ref8">8</xref>] . New or severely disturbed sites with no seeds or vegetative propagules develop by primary succession, while sites that lack surface vegetation but have a seedbank or vegetative propagules develop by secondary succession. Reestablishment of plant cover through natural succession events is a significantly longer and slower process in the arctic than in more temperate climates, with estimates of 100 or more years to achieve former plant diversity and coverage [<xref ref-type="bibr" rid="scirp.56743-ref6">6</xref>] -[<xref ref-type="bibr" rid="scirp.56743-ref10">10</xref>] . In previous studies monitoring natural revegetation in the Arctic, the first plants to re-colonize disturbed areas are the most efficient seed (e.g. Drabaspp, Oxyriadigyna, and several grasses) or bulbil producers (e.g. Polygonum viviparum and Saxifraga spp.) [<xref ref-type="bibr" rid="scirp.56743-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref11">11</xref>] . Slow-growing woody perennials such as Dryas integrifolia, Salix arctica, and Saxifraga oppositifolia are often undetectable or do not provide significant plant cover until much later in the natural succession process, if at all [<xref ref-type="bibr" rid="scirp.56743-ref11">11</xref>] -[<xref ref-type="bibr" rid="scirp.56743-ref13">13</xref>] . As species turnover is low in arctic and alpine ecosystems, early colonizing species may become part of the late successional stage. Regeneration of plant cover can be further inhibited by factors such as unviable seeds, herbivory, soil compaction, and substrate instability [<xref ref-type="bibr" rid="scirp.56743-ref5">5</xref>] -[<xref ref-type="bibr" rid="scirp.56743-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref14">14</xref>] . Understanding expected successional pathways following disturbances can help accelerate revegetation by identifying factors limiting species establishment and growth [<xref ref-type="bibr" rid="scirp.56743-ref15">15</xref>] .</p><p>Assisted revegetation is an active process in which seeds from native or non-native species are selectively sowed, and/or cuttings from slow-growing woody perennial shrubs are planted onto disturbed areas to accelerate the rate of plant coverage. Species selection following disturbance is based on revegetation goals and objectives. For ecological restoration, the goal is to develop self-supporting vegetation with similar structure, function and plant communities as found in the original environment [<xref ref-type="bibr" rid="scirp.56743-ref16">16</xref>] . In comparison, reclamation of disturbed land aims to control erosion, provide immediate forage for herbivores, improve aesthetics and/or prevent encroachment of invasive species using native or non-native species [<xref ref-type="bibr" rid="scirp.56743-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref17">17</xref>] . Various studies of assisted revegetation using seeds and tillers of grasses and other graminoid plants, legumes, and cuttings of Salix ssp. have been conducted in northern Alaska, Canada, Greenland, Iceland and north-west Siberia to quickly cover disturbed areas and to</p><fig-group id="fig1"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Location of DYE-M, Cape Dyer, Nunavut. Bottom figure shows the locations of the Upper (Radar station), Lower (Logistics and housing), and Beach (revegetation area) sites at DYE-M.</title></caption><fig id ="fig1_1"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/18-2602037x6.png"/></fig><fig id ="fig1_2"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/18-2602037x7.png"/></fig></fig-group><p>re-establish a plant community (reviewed in [<xref ref-type="bibr" rid="scirp.56743-ref6">6</xref>] ). In particular, Lolium multiflorum (annual ryegrass) has been used as a “nurse grass” in previous remediation projects in Alaska and the Yukon to help prevent further erosion by establishing an immediate plant community, improve nutrient content in the top layer of the soil, create safe microenvironments to enhance germination, and provide windbreaks to help trap native seeds blowing across unvegetated areas of the site [<xref ref-type="bibr" rid="scirp.56743-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref19">19</xref>] . When possible, the use of native species is preferred as they are more adapted to the environment and will generally blend in better with the surrounding areas. However, as it can be difficult to obtain appropriate seeds or plant material in sufficient quantities to remediate large areas [<xref ref-type="bibr" rid="scirp.56743-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref17">17</xref>] , reclamation and ecological restoration in the north following disturbance have not yet been achieved with much success.</p><p>A four-year revegetation project was undertaken at the DYE-M beach site between 2009 and 2012 to accelerate recovery of disturbed areas. The short-term objective was to investigate the feasibility of, and devise a plan to, accelerate revegetation of disturbed areas through assisted seed dispersal and selective transplantation of slow-growing shrub species. The long-term goal was to monitor successional changes towards achievement of comparable species biodiversity and vegetation coverage in the disturbed and surrounding areas at this arctic site.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Ecoclimate Characteristics</title><p>DYE-M has a high arctic ecoclimate with long cold winters with an average winter temperature of −22.5˚C, an annual temperature of −11.5˚C and short, very cold summers with an average summer temperature of 1˚C [<xref ref-type="bibr" rid="scirp.56743-ref20">20</xref>] . Annual precipitation is approximately 200 - 400 mm in the ecoregion, with deep continuous permafrost, bare rock and turbic cryosols. Vegetation has low diversity and sparse cover, with a mix of low-growing herbs, shrubs, heath species, mosses and lichens.</p></sec><sec id="s2_2"><title>2.2. Initial Site Assessments</title><p>Plant surveys were completed in July 2009 at DYE-M to determine the density and biodiversity of different species growing in the undisturbed areas surrounding the disturbed area at the beach to define a baseline for the project and a long-term goal for revegetation. Six transects (40 - 100 m long) were established in undisturbed areas, and quadrats (1-m<sup>2</sup>) were set up every 10 m along each transect (n = 60) to determine the percent coverage of each plant species and the percent of bare soil/rocks. Plants were identified using Barrenland Beauties [<xref ref-type="bibr" rid="scirp.56743-ref21">21</xref>] and Vascular Plants of Continental Northwest Territories, Canada [<xref ref-type="bibr" rid="scirp.56743-ref22">22</xref>] , and identifications were verified by an independent plant expert at Queen’s University (Supplementary Information <xref ref-type="table" rid="table1">Table 1</xref>).</p><p>Two soil samples were collected from the disturbed area (0 - 10 cm) and two from the undisturbed surrounding</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Plant species observed on the beach area of Cape Dyer, July 2009</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Latin Name</th><th align="center" valign="middle" >Common Name</th><th align="center" valign="middle" >Root Structure</th><th align="center" valign="middle" >Shoot Structure</th><th align="center" valign="middle" >Reproductive Method</th></tr></thead><tr><td align="center" valign="middle" >Armeriamaritimasubsp. sibirica (Turcz. Ex Boiss.) Nyman</td><td align="center" valign="middle" >sea pink/thrift</td><td align="center" valign="middle" >taproot</td><td align="center" valign="middle" >evergreen perennial</td><td align="center" valign="middle" >seeds</td></tr><tr><td align="center" valign="middle" >Carex bigelowii (Torr ex Schwein)</td><td align="center" valign="middle" >sedge</td><td align="center" valign="middle" >fibrous</td><td align="center" valign="middle" >perennial herb-graminoid</td><td align="center" valign="middle" >rhizomes/stolons/achenes</td></tr><tr><td align="center" valign="middle" >Cassiopetetragona (L.) D. Don</td><td align="center" valign="middle" >white Arctic heather/Arctic bell heather</td><td align="center" valign="middle" >fibrous roots along stem</td><td align="center" valign="middle" >dwarf shrub-evergreen</td><td align="center" valign="middle" >seeds</td></tr><tr><td align="center" valign="middle" >Cerastium uniflorum Clairv.</td><td align="center" valign="middle" >glacier mouse-ear chickweed</td><td align="center" valign="middle" >Fibrous</td><td align="center" valign="middle" >forb</td><td align="center" valign="middle" >seeds</td></tr><tr><td align="center" valign="middle" >Chamerion latifolium (L.) Holub</td><td align="center" valign="middle" >river beauty/dwarf fireweed/ broad-leafed willow herb</td><td align="center" valign="middle" >fibrous</td><td align="center" valign="middle" >perennial herb-forb</td><td align="center" valign="middle" >rhizomes/seeds</td></tr><tr><td align="center" valign="middle" >Dryas octopetala L.</td><td align="center" valign="middle" >mountain avens</td><td align="center" valign="middle" >taproot/lateral roots from stem</td><td align="center" valign="middle" >dwarf shrub</td><td align="center" valign="middle" >fruit, branches root</td></tr><tr><td align="center" valign="middle" >Empetrum nigrum L.</td><td align="center" valign="middle" >crowberry</td><td align="center" valign="middle" >lateral roots from stem</td><td align="center" valign="middle" >dwarf shrub evergreen</td><td align="center" valign="middle" >seeds in fruit/branches root</td></tr><tr><td align="center" valign="middle" >Hierochloe alpine (Sw. ex Willd.) Roem. &amp; Schult.</td><td align="center" valign="middle" >holy grass</td><td align="center" valign="middle" >fibrous</td><td align="center" valign="middle" >graminoid</td><td align="center" valign="middle" >rhizomes, seeds</td></tr><tr><td align="center" valign="middle" >Luzula confusa (Lindeberg)</td><td align="center" valign="middle" >northern woodrush</td><td align="center" valign="middle" >fibrous</td><td align="center" valign="middle" >perennial herb-graminoid</td><td align="center" valign="middle" >rhizomes/seeds</td></tr><tr><td align="center" valign="middle" >Oxyria digyna (L.) Hill</td><td align="center" valign="middle" >mountain sorrel</td><td align="center" valign="middle" >taproot</td><td align="center" valign="middle" >perennial herb-forb</td><td align="center" valign="middle" >rhizomes/seeds</td></tr><tr><td align="center" valign="middle" >Papaver radicatum L.</td><td align="center" valign="middle" >Arctic poppy</td><td align="center" valign="middle" >fibrous/taproot</td><td align="center" valign="middle" >perennial herb-forb</td><td align="center" valign="middle" >seeds</td></tr><tr><td align="center" valign="middle" >Polygonum viviparum L.</td><td align="center" valign="middle" >alpine bistort</td><td align="center" valign="middle" >fibrous</td><td align="center" valign="middle" >perennial herb</td><td align="center" valign="middle" >bulbils/fragmentation rhizomes/achenes</td></tr><tr><td align="center" valign="middle" >Salix arctica Pall.</td><td align="center" valign="middle" >Arctic willow</td><td align="center" valign="middle" >lateral roots from stem</td><td align="center" valign="middle" >dwarf shrub</td><td align="center" valign="middle" >seeds/branches root</td></tr><tr><td align="center" valign="middle" >Silene acaulis L. Jacq.</td><td align="center" valign="middle" >moss campion</td><td align="center" valign="middle" >taproot</td><td align="center" valign="middle" >perennial herb- forb-cushion plant</td><td align="center" valign="middle" >rhizomes, seeds, stolons</td></tr><tr><td align="center" valign="middle" >Vaccinium uliginosum L.</td><td align="center" valign="middle" >whortleberry/bilberry</td><td align="center" valign="middle" >roots along stem</td><td align="center" valign="middle" >dwarf shrub</td><td align="center" valign="middle" >seeds</td></tr></tbody></table></table-wrap><p>area and analyzed for total organic carbon (TOC) and particle sizeto determine if there were differences in the soil composition that might affect revegetation.</p></sec><sec id="s2_3"><title>2.3. Revegetation Techniques</title><sec id="s2_3_1"><title>2.3.1. Site Preparation</title><p>A loader tractor with a tooth bucket was used to create grooves across the disturbed area which had been heavily compacted by machinery. Grooves were created by dragging the bucket perpendicular to the direction of prevailing winds, creating ridges approximately 10 - 15 cm deep, and 20 cm apart. In 2009, it was suggested by an on-site remediation design engineer that a section of the disturbed area be amended with an Agrico Canada Ltd fertilizer (available in large quantities at the site for hydrocarbon remediation in landfarms) prior to seeding. As the disturbed areas overlooked Exeter Bay, the use of this fertilizer was deemed inappropriate for this project since the MSDS literature indicated potential harm to aquatic organisms.</p></sec><sec id="s2_3_2"><title>2.3.2. Salix arctica Transplantation Techniques</title><p>Salix arctica Pall. (willow) cuttings were harvested from a donor population near the beach after a frost in Sep- tember 2009. A shoot segment 30 - 150 cm long and ~1 - 2 cm in diameter was cut from the stem of each donor willow plant with pruning shears, and kept in water until time of transplantation (&lt;10 hrs). Longer cuttings (&gt;40 cm) were further separated into two or more cuttings before transplantation as recommended by Walter et al. [<xref ref-type="bibr" rid="scirp.56743-ref23">23</xref>] . Cuttings were folded in three, and then buried in holes (10 - 15 cm deep) that were created on an angle with a pick-axe (R. Lewis 2009, personal conversation). Care was taken to ensure that one or two leaf buds were above the surface of the soil. A total of 540 willow cuttings were planted in 26 plots of 12, 16, 20 or 25 cuttings(based on space and amount of collected material) to create small “islands” within the unvegetated area to accelerate growth of these slow-growing woody perennial species. Four to five cuttings were planted in a row, with four to five rows per plot. Cuttings were planted approximately 50 - 100 cm apart within a row, and the next row was offset by approximately 50 - 100 cm so cuttings in two adjacent rows were not directly in line creating a diamond-shaped pattern as recommended by Walter et al. [<xref ref-type="bibr" rid="scirp.56743-ref23">23</xref>] . The use of islands was chosen as a revegetation strategy as the areal extent of the unvegetated areas was too large to economically cover completely with cuttings [<xref ref-type="bibr" rid="scirp.56743-ref24">24</xref>] . Plots were randomly distributed across the disturbed area with cuttings located on flat and sloped areas.</p><p>Another 150 cuttings were transplanted in the fall of 2011. Cuttings were again collected following a frost from donor plants located in areas surrounding the disturbed area. Five plots were planted with 27 - 30 willow cuttings using the same method as those planted in 2009, whereas a sixth plot was planted with a modified approach in which willows were planted in long trenches in a staggered pattern so plants could lie in their natural orientation and nodal root growth could be encouraged [<xref ref-type="bibr" rid="scirp.56743-ref23">23</xref>] . These longer and shallower trenches were at times easier to dig in the rocky ground than vertical holes (as buried boulders need to be moved or planting sites repeatedly shifted). In addition to burying three quarters of the plant cutting in soil to encourage root development, the existing secondary root structures along the exposed region of the cutting were covered with small mounds of soil to promote nodal root development.</p></sec><sec id="s2_3_3"><title>2.3.3. Seed Collection and Seeding Techniques</title><p>Twenty-two kg of Lolium multiflorum (annual ryegrass; Lot L19-8-22G) obtained from Country Depot in Kingston Ontario, was seeded by hand across ~7900 m<sup>2</sup> of the disturbed area at a rate of 29 kg/ha (commercial seeding rates = 15 - 30 kg/ha).</p><p>Ripe seeds and berries from native plants were collected by hand into five large ziplock bags (3.8 L each) from the areas above and below the disturbed area. Seeds were of different shapes, sizes, and weights based on their dispersal mechanisms. Each bag contained a different mix of seeds and berries based on the collection area; therefore seed density was not calculated prior to dispersal. Native seed was mixed by hand to create a more homogenous mix of seeds and berries and then dispersed by hand on the same area (~7900 m<sup>2</sup>) as the annual ryegrass. Seeds were not tested for germination prior to dispersal. Future studies are required to investigate seed germination and seedling survival for seeds from this area. Following seed dispersal (native and non-native), seeds were covered with soil by attaching a large metal fence section (~4 feet &#215; 5 feet) to the back of an all-terrain vehicle, and dragging it perpendicular to the direction of the ridges to help push loose soil into the grooves to cover the seeds.</p></sec></sec><sec id="s2_4"><title>2.4. Monitoring</title><sec id="s2_4_1"><title>2.4.1. Willow Cuttings</title><p>Plantassessments were conducted in late July and early August in 2010, 2011, and 2012 to determine the number of Salix arctica cuttings that survived the winter and produced new shoot growth. New shoot growth was qualified as the observation of one or more leaves, and quantified in 2010 as, i) limited growth (1-2 leaves), ii) moderate growth (3 - 4 leaves) and iii) significant growth (4+ leaves). In 2011 and 2012, cuttings were determined to be alive (one or more leaves) or dead (no leaves). Four cuttings were excavated in 2010 to observe root growth from one plant with limited growth, one plant with moderate growth, and two plants with significant growth.</p></sec><sec id="s2_4_2"><title>2.4.2. Seedling Germination and Species Biodiversity</title><p>Based on slow growth rates of Arctic plants, where most species are still relatively small during the first growing seasons [<xref ref-type="bibr" rid="scirp.56743-ref25">25</xref>] , the use of &gt;20% frequency rather than &gt;2% ground cover or &gt;10 stems/m<sup>2</sup> was chosen to measure initial success for the establishment of seedlings on the remediated areas at DYE-M in 2010, 2011 and 2012 [<xref ref-type="bibr" rid="scirp.56743-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref27">27</xref>] . Twenty-eight transects and 136 1-m<sup>2</sup> quadrats were systematically established across the disturbed area in 2010to identify native plant species frequency and biodiversity. A more detailed assessment was conducted in 2011 using systematic transects and 379 1-m<sup>2</sup> quadrats [<xref ref-type="bibr" rid="scirp.56743-ref28">28</xref>] . Due to time and weather constraints, only 15 1-m<sup>2</sup> quadrats were randomly established for monitoring in 2012. Loliummultiflorum was only assessed in 2010 as it is an annual species. Lolium multiflorum frequency and density were assessed in 2010 by counting individual plants in each quadrat.</p></sec></sec></sec><sec id="s3"><title>3. Results and Discussion</title><sec id="s3_1"><title>3.1. 2009 Initial Plant Survey Results</title><p>Results from the initial survey of the surrounding area vegetation (i.e. prior to revegetation efforts) determined that on average, ~68% of each quadrat at DYE-M was bare soil or rock, and the remaining ~32% was a mixture of fifteen plant species (<xref ref-type="fig" rid="fig2">Figure 2</xref>). Plants identified at DYE-M were a mixture of woody perennial shrub-heath species, graminoids, and herbaceous perennial plants, though the three species with the most ground cover were Salix arctica (~11%), Vaccinium uliginosum L. (~8%), and Empetrum nigrum L. (~5%), all of which are woody perennial species (Supplementary Information <xref ref-type="table" rid="table1">Table 1</xref>). In the arctic, the majority of plants tend to be perennial herbs, slow-growing woody-shrubs, or mosses and lichens, with very few annual species. Grasses and S. arctica were the most frequent species at DYE-M, appearing in 48 and 45 of the 60 quadrats, respectively (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Visual surveys of the disturbed areas at DYE-M noted virtually no new plant growth.</p><p>Of the fifteen species observed on site in 2009, seven had fibrous root systems, four had taproot systems, and five were able to produce roots from prostrate shoot branches (Supplementary Information <xref ref-type="table" rid="table1">Table 1</xref>). Shoot structures of arctic plants tend to be low-lying forms that maximize plant exposure to sunlight, while minimizing the impact of low temperatures and strong winds. Low-lying plants are further protected during winter months by a snow cover that insulates them from extreme thermal and moisture conditions [<xref ref-type="bibr" rid="scirp.56743-ref29">29</xref>] . At DYE-M, plants generally had short and flexible shoot systems or were low-lying, woody perennials. Due to the short growing season, most species were flowering or nearing the end of their flowering period during the survey period in mid-July. In general, perennial species produce flower and leaf buds in the fall in preparation for the following season, before going dormant for the winter [<xref ref-type="bibr" rid="scirp.56743-ref5">5</xref>] .</p><p>Soil analysis determined that the particle size ranged from &gt;0.001 mm to &gt;4 mm; the majority of particles were &lt;4 mm. Soil type was a mixture of sand (68%), gravel (17%), silt (11%), and clay (4%). Total organic carbon in the soil ranged from 0.22 to 0.91 for the reshaped areas, and from 0.68 to 0.86 for nearby samples from the undisturbed areas. These values are similar to carbon storage values reported for “c” horizons in various tundra environments, and for upper soil horizons in barren ground mountain tops, river gravel bar and alpine slope soil in Alaska [<xref ref-type="bibr" rid="scirp.56743-ref30">30</xref>] .</p><p>Fertilizer has historically been scattered across disturbed areas during site closures in northern locations to decrease the amount of material that must be shipped back down south and to potentially improve revegetation of the disturbed areas. While fertilizer was not used in this project due to proximity to the aquatic environment,</p><p>the use of fertilizers is often deemed necessary in arctic revegetation projects to promote plant growth, especially for non-native species, as the uppermost soil layer which generally contains nutrients and soil bacteria that</p><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Mean percent coverage of the eight most common plant species across all quadrats</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/18-2602037x8.png"/></fig><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Frequency of species detected in quadrats between 2009 and 2012. Species identified in 2009 are from undisturbed locations. Species from 2010-2012 are from disturbed areas</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/18-2602037x9.png"/></fig><p>help cycle nutrients has generally been disturbed or removed by human activities [<xref ref-type="bibr" rid="scirp.56743-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref17">17</xref>] . However, in some arctic environments, the use of fertilizers may be detrimental to some plants that are adapted to growing in nutrient-poor environments, or if non-native species become established due to a higher nutrient content, they may prevent re-colonization by native species through formation of a dense vegetation mat that is not easily penetrated [<xref ref-type="bibr" rid="scirp.56743-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref31">31</xref>] . For example, a study by Klokk and R&#248;nning [<xref ref-type="bibr" rid="scirp.56743-ref10">10</xref>] , determined that the effectiveness of fertilizer treatments on seven native species in Norway appeared to be species-specific. In future, controlled experiments conducted on a site-specific basis would be required to determine if fertilizer would benefit revegetation efforts at a specific site in the Arctic.</p><sec id="s3_1_1"><title>3.1.1. Species Selection for Revegetation at DYE-M</title><p>Prior to revegetation efforts at DYE-M, all fifteen species observed in the initial study were investigated to determine their revegetation potential based on: i) their ability to tolerate sandy soil, ii) their potential to improve the growth substrate, iii) whether they were perennials, iv) whether they were native to the Cape Dyer region, v) whether they could be obtained commercially or locally in sufficient quantities, vi) whether they had previously been shown to be successful in revegetation studies, and vii) whether they had the ability to prevent further erosion on the site (adapted from [<xref ref-type="bibr" rid="scirp.56743-ref7">7</xref>] ). Of the fifteen identified species, all were perennial and capable of reproducing by seeds or achenes, and some could also reproduce by rhizomes, stolons and rooting from prostrate shoots (Supplementary Information <xref ref-type="table" rid="table1">Table 1</xref>). Based on recommendations by R. Lewis from Arctic Alpine Seed Ltd (personal conversation, 2009) and the criteria above, it was determined that seeds from all species observed at Cape Dyer would be collected from the surrounding areas for assisted seed dispersal as commercial sources of native arctic seeds were not available in sufficient quantities. In addition, Lolium multiflorum(annual ryegrass) was recommended as a nurse species to help prevent erosion and to improve the nutrient content in the soil.</p></sec></sec><sec id="s3_2"><title>3.2. Revegetation Results 2010-2012</title><sec id="s3_2_1"><title>3.2.1. Survival Rate and Growth of Salix arctica Cuttings 2010-2012</title><p>Ninety-four percent of the 540 S. arctica cuttings planted in 2009 survived the winter and produced new shoot growth in 2010. First year survival rates greater than 80% are considered successful for Salix sp. cuttings [<xref ref-type="bibr" rid="scirp.56743-ref32">32</xref>] , while Densmore et al. [<xref ref-type="bibr" rid="scirp.56743-ref33">33</xref>] reported survival rates between 86% - 96% for different lengths of Salix alaxensis cuttings after one year of growth in Alaska. In this study, S. arctica cuttings continued to develop new shoot growth after initial observations in mid-July. Catkins were observed on some plants during the survey period.</p><p>Root growth assessments determined that roots ranged in length from non-existent (plant with limited shoot growth), to extensive (plant with significant shoot growth) with roots &gt;10 cm long and secondary and tertiary root development. Maximum root growth was observed in damp but not flooded areas. Visual observations of S. arctica from other areas around the site support the observation that plant growth is greatest in areas that offer refuge from strong winds (along rocks and boulders), as well as providing a significant source of soil water content (near water pools and along water run-off areas). Furthermore, these S. arctica tend to have well-developed secondary root growth along the full length of the stem (<xref ref-type="fig" rid="fig4">Figure 4</xref>).</p><p>In 2011, two landslides, one in June and one in late August, carrying rock and sediment debris from the road and hillside above the beach impacted six of the revegetation plots. Only thirty-five of the 88 willow cuttings from these plots survived. Initial observations from late July indicated that most cuttings in the other areas were producing leaves, but that secondary root development and shoot length growth was limited. This is to be expected as growth in the arctic is slow and significant change in size may take years of observation. Plant surveys were conducted six weeks later in September, and it was determined that some cuttings that had been judged unsuccessful in July had multiple leaves and appeared to be in significantly better health. Based on the September observations, 84% of the 428 S. arctica cuttings found in 2011 had survived since 2009. Results from 2010 and 2011 indicate that end-of-season observations provide a more realistic indication of overall plant health and survivorship than early or mid-season observations.</p><p>Plant surveys were conducted in August 2012, following another landslide in July which impacted a similar area as in 2011. Another two plots were compromised by this third landslide, leaving only 29 of the 128 willows in this area. In addition, road work destroyed another two plots (24 cuttings). Of the remaining 388 cuttings not impacted by landslides or other disturbances, 82% survived to year three. This three year survival rate of 82% is similar to observations from a revegetation effort following an oil spill along the Trans-Alaska pipeline in 2001, where 80% - 88% of transplanted willow cuttings survived after three years [<xref ref-type="bibr" rid="scirp.56743-ref34">34</xref>] . Observations of surviving plants at DYE-M indicated that many plants were starting to produce new stem tissue as well as new leaves, with many plants having 50+ leaves by the start of August, 2012. However, Densmore et al. [<xref ref-type="bibr" rid="scirp.56743-ref33">33</xref>] reported that long-term survival dropped to 53% after nine years, indicating that long-term monitoring and further transplantation of cuttings may be necessary to ensure long-term revegetation success. Of the 178 new cuttings planted in 2011, 93% survived the first winter and were producing leaves in 2012, indicating similar one year success as the first set of cuttings. The sixth plot planted with the alternative method had the lowest survival rate (89%), but the surviving plants had the most leaves along the aboveground shoot tissue. Encouragement of nodal adventitious roots has been shown to significantly increase stem length in Cucurbita pepo L. [<xref ref-type="bibr" rid="scirp.56743-ref35">35</xref>] . Methods to optimize root development and formation along stem tissues require further investigation in shrub species.</p></sec><sec id="s3_2_2"><title>3.2.2. Lolium multiflorum (Annual Ryegrass) Results</title><p>Lolium multiflorum (annual ryegrass) seeded at a planted density of ~29 kg/ha in 2009, was observed in 85% of</p><fig-group id="fig4"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> (a) One-year-old Salix arctica cutting with significant shoot growth; (b) Root system developing along underground portions of the transplanted stem cutting; (c) Close-up of root development (~10 cm).</title></caption><fig id ="fig4_1"><label> (b)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/18-2602037x10.png"/></fig><fig id ="fig4_2"><label> (c)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/18-2602037x11.png"/></fig><fig id ="fig4_3"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/18-2602037x12.png"/></fig></fig-group><p>all quadrats, with a maximum density of 198 plants/100 cm<sup>2</sup>. While the majority of L. multiflorum germinated and grew in 2010, a minority of seeds germinated in 2011 and 2012. No plants had developed spikes or inflorescences by the end of July, 2010, and all plants appeared so be stunted by the cold climate, with heights between 5 - 10 cm, in comparison to normal heights up to 125 cm [<xref ref-type="bibr" rid="scirp.56743-ref36">36</xref>] . The majority of plants were observed in furrows or around the edges of boulders where they were slightly protected from the wind. Dead shoot tissue from plants that grew in 2010 was no longer present in 2012. This material is expected to help introduce organic material into the top layer of soil. Thus while seeding densities of L. multiflorum between 3.5 to 30 kg/ha have been used in previous studies [<xref ref-type="bibr" rid="scirp.56743-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref38">38</xref>] , a higher planting density may be necessary in extremely exposed Arctic environments when used for erosion prevention and/or as nurse grass for native species to ensure growth of a sufficient quantity of shoot material. However, care must be taken to ensure that the selected species is not seeded too densely or it might prevent germination and growth of native species, particularly if it is a perennial species [<xref ref-type="bibr" rid="scirp.56743-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.56743-ref39">39</xref>] .</p></sec><sec id="s3_2_3"><title>3.2.3. Native Species Seeding Results</title><p>Previous studies have used various guidelines to determine the success of revegetation projects, including colonization by native plants and establishment of seedlings, increased species diversity, reproduction by colonizing species, development of a moss layer, accumulation of ground litter, and 85% total plant cover [<xref ref-type="bibr" rid="scirp.56743-ref40">40</xref>] -[<xref ref-type="bibr" rid="scirp.56743-ref43">43</xref>] . Quantitative criteria used by Kershaw and Kershaw [<xref ref-type="bibr" rid="scirp.56743-ref27">27</xref>] , and Rausch and Kershaw [<xref ref-type="bibr" rid="scirp.56743-ref7">7</xref>] to evaluate successful colonizers of long-term natural revegetation projects under extreme growth conditions included species that met at least one of, &gt;2% ground cover, &gt;20% frequency, or &gt;10 stems/m<sup>2</sup>. Seedlings and plants from 14 species were observed in the quadrats or along transects between 2010 and 2012, in comparison to the 15 species recorded from plant surveys of the surrounding areas in 2009. Ground cover was not determined on an individual or total species basis during the surveys due to the low species diversity per plot and small size of plants. Of the 14 species observed during these three years, Chamerion latifolium (L.) Holub was the only species to have greater than 20% frequency every year, including in 2009 (22% - 67%), (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Other species with greater than 20% frequency during at least one year of monitoring included Cerastium uniflorum Clairv. (11% - 47%), mixed grasses (14% - 100%), Montia fontana L. (0% - 33%), Papaver radicatum Rottb. (2% - 73%), S. arctica (15% - 75%), and Silene acaulis (L.) Jacq. (7% - 42%) (<xref ref-type="fig" rid="fig3">Figure 3</xref>).</p><p>New species observed on the disturbed areas included Cochlearia officinalis L., Melandrium affine (J. Vahl ex Fr.) J. Vahl, and M. fontana [<xref ref-type="bibr" rid="scirp.56743-ref21">21</xref>] , while slow-growing heath-shrub species Cassiope tetragona (L.) D. Don, Dryas octopetala L., Empetrum nigrum, and Vaccinium uliginosum were not recorded on the remediated areas. In temperate locations, plant communities develop over time through a series of natural succession events, whereby initial colonizing species are gradually replaced by other species, often with slower dispersion techniques [<xref ref-type="bibr" rid="scirp.56743-ref44">44</xref>] . All 14 species observed in the remediated areas have wind or bird-dispersed seeds or produce bulbils, helping them to colonize disturbed areas in the first phase of plant succession. In natural environments following disturbance such as fire, the soil seed bank can accelerate site recovery, as seed banks generally represent the established vegetation in the area with the exception of woody perennial species [<xref ref-type="bibr" rid="scirp.56743-ref45">45</xref>] . However, this area has a history of repetitive disturbances, and the minimal topsoil that may have been present on the disturbed areas was not salvaged prior to landfill excavation. In future, preservation of this top layer of soil could introduce seeds and organic matter which can accelerate development of a natural plant community and provide the most widespread initial coverage, leading to long-term soil stability. This is particularly important in the Eastern Arctic, where no commercial seed mixture is currently available.</p><p>Despite the harsh climate and unpredictable weather patterns in the arctic that make revegetation work difficult, visual observations of the disturbed areas in 2012 indicated that patches of new vegetation are becoming more predominant compared to the almost complete lack of vegetation in 2009. Arctic plant communities are slow growing and seedling distribution tends to be skewed towards those sites that offer favourable conditions and are in close proximity to native tundra. Germination sites or microsites may be created naturally such as by desiccation cracks in the ground [<xref ref-type="bibr" rid="scirp.56743-ref46">46</xref>] , or may be created with assistance. For example, Cater et al. [<xref ref-type="bibr" rid="scirp.56743-ref37">37</xref>] used a track vehicle to scarify the ground prior to seeding. These microsites are important for trapping seeds during dispersal, and also create a microclimate with specific properties favoured by plants including a greater mean soil temperature, lower wind speed, increased soil moisture and superior soil nitrate levels [<xref ref-type="bibr" rid="scirp.56743-ref46">46</xref>] . In this study, most seedlings were initially observed growing within furrows or around windbreaks such as the edges of rocks, as seeds were less likely to be blown or washed away, and/or sheltered within depressions, which provide suitable microclimates for germination and growth. However, the furrows created in 2009 had almost completely been smoothed over by 2012. A higher density of new seedlings was also observed around S. arctica patches, indicating that S. arctica “islands” are likely trapping seeds blowing across the unvegetated areas, and providing safe sites and microclimates that enhance seed germination and seedling growth. In addition, shrub species such as S. arctica may protect and insulate herbaceous species during the winter from extreme temperatures and winds by trapping snow in the branches, which promotes plant establishment [<xref ref-type="bibr" rid="scirp.56743-ref47">47</xref>] . Thus initial observations indicate that loosening soil prior to seeding and creating S. arctica islands enhances revegetation and may increase the probability of long term success.</p></sec></sec></sec><sec id="s4"><title>4. Conclusion</title><p>As seedling growth is a slow process, monitoring over ten or more years will likely be required before conclusively declaring the disturbed areas partially or wholly revegetated. The information and techniques developed for this project can be used to guide the long-term remediation and revegetation strategies at other DEW line and high arctic sites following large scale disturbances. Future studies could incorporate assessment of native seed germination and survival rates, germination rates from the seedbank, permanent monitoring plots and use of other shrub species to improve diversity and long term monitoring of disturbed sites.</p></sec><sec id="s5"><title>Acknowledgements</title><p>The authors are indebted to members of the Environmental Sciences Group (ESG) who have been involved in the DYE-M Clean up project over the years. We are grateful for the help provided in the field, and for the funding provided by North Warning System Office (NWSO) for this project.</p></sec><sec id="s6"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.56743-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Royal Roads Military College Environmental Science Group (RRMC ESG) (1991) North Warning System Environmental Study, v. 1 Overview. 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