<?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.2018.92016</article-id><article-id pub-id-type="publisher-id">AJPS-81986</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>
 
 
  Effect of Autumn Cutting Date on Regrowth, Turning Green, Yield and Quality of &lt;i&gt;Leymus chinensis&lt;/i&gt; Grassland in Songnen Plain, Northeast China
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yantao</surname><given-names>Song</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>&amp;ensp;</surname><given-names>Wuyunna</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>Daowei</surname><given-names>Zhou</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, Changchun, China</addr-line></aff><aff id="aff1"><addr-line>College of Environment and Bioresources, Dalian Minzu University, Dalian, China</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>yantaosong@dlnu.edu.cn(YS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>18</day><month>01</month><year>2018</year></pub-date><volume>09</volume><issue>02</issue><fpage>185</fpage><lpage>195</lpage><history><date date-type="received"><day>5,</day>	<month>December</month>	<year>2017</year></date><date date-type="rev-recd"><day>22,</day>	<month>January</month>	<year>2018</year>	</date><date date-type="accepted"><day>25,</day>	<month>January</month>	<year>2018</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>
 
 
  A field study was carried out to quantify the effects of different cutting time on 
  Leymus chinensis
   population and community characteristic in Songnen grassland of northeast China from August, 2006 to August, 2007. The treatment interval was ten days with the remaining stubble height of 5 cm from 15th August to 4th October in 2006. Results showed that the 
  L. chinensis
   made up about 90% of the dry matter of aboveground biomass, and there were about ten species in the 
  L. chinensis
   community in the 1 m &#215; 1 m plot. The 
  L. chinensis 
  and
   Kalimeris integrifolia
   regrew rapidly after autumn cutting in 2016. In the second year, the coefficients of the community similarity were high between the different cutting time treatments. The density, height, aboveground biomass, stem/leaf ratio, and crude protein of 
  L. chinensis 
  were not significant at the turning green stage and harvesting stage, the companion species of 
  L. chinensis
   community contained higher crude protein, but the crude protein of the plant community were not significant. Thus, considering the weather factor for haymaking, the harvest dates should be concentrated from the middle ten days of August to the first ten days in September.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Leymus chinensis&lt;/i&gt;</kwd><kwd> Autumn Cutting</kwd><kwd> Hay Yield</kwd><kwd> Quality</kwd><kwd> Songnen Grass-land</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The Songnen plain covers the western parts of Heilongjiang, Jilin and Liaoning provinces of northeastern of China, existing an area of about 170,000 km<sup>2</sup> (43˚30' to 48˚40'N; 121˚30' to 127˚00'E), about 40% of which is Leymus chinensis grassland [<xref ref-type="bibr" rid="scirp.81986-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref2">2</xref>] . L. chinensis is a perennial rhizome grass and widely distributes in the eastern end of the Eurasian steppe zone, with the main locations in China being in the Songnen plain and the eastern part of the Inner Mongolian plateau [<xref ref-type="bibr" rid="scirp.81986-ref3">3</xref>] . This species is ideal for grazing and forage because of its high palatability and nutrition [<xref ref-type="bibr" rid="scirp.81986-ref4">4</xref>] . The usual growing conditions in Songnen plain produce superior herbage both in quality and in quantity, thus, this type of grassland is one of the best suited in northern China for the grazing land or cutting field [<xref ref-type="bibr" rid="scirp.81986-ref5">5</xref>] .</p><p>The climate type of Songnen plain is a semi-arid, temperate continental monsoon, the winter is long and cold, the summer is short and warm, the raining period concentrates on from June to August, the growing season in this region is mainly from April to October [<xref ref-type="bibr" rid="scirp.81986-ref6">6</xref>] . And the primary productivity is correlative with environmental factors [<xref ref-type="bibr" rid="scirp.81986-ref7">7</xref>] , especially the precipitation from April to July or aridity index [<xref ref-type="bibr" rid="scirp.81986-ref8">8</xref>] . The primary productivity of the forages reaches the maximum usually at the middle or last ten days of August [<xref ref-type="bibr" rid="scirp.81986-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref10">10</xref>] .</p><p>Cutting is one of the main ways to utilize and manage grassland [<xref ref-type="bibr" rid="scirp.81986-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref12">12</xref>] , this way can supply the forage for livestock in winter and next spring and make sure them live through the long and cold winter [<xref ref-type="bibr" rid="scirp.81986-ref13">13</xref>] , and cutting once per year is advisable in Songnen grassland [<xref ref-type="bibr" rid="scirp.81986-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref14">14</xref>] , because cutting two times a year would lead some harmful effects on the yield and environment of the grassland even adding the fertilizer and water to the grassland [<xref ref-type="bibr" rid="scirp.81986-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref16">16</xref>] . So the farmer usually harvests the forage from later summer to early winter in order to gain the maximal yield and quality，and this is the best time for making hay of Songnen grassland because of the good weather, and the height of the remaining stubble usually is 4 - 5 cm [<xref ref-type="bibr" rid="scirp.81986-ref5">5</xref>] . But different cutting dates may not only effect on the grass regrowth, and biomass at the current year [<xref ref-type="bibr" rid="scirp.81986-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref19">19</xref>] , but also effect on the turning green date, biomass, layering distribution of the biomass for the next year [<xref ref-type="bibr" rid="scirp.81986-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref20">20</xref>] . Previous studies have showed that all the cutting dates run through the whole growing season, such as moderate levels of spring defoliation could improve winter range forage quality [<xref ref-type="bibr" rid="scirp.81986-ref21">21</xref>] , cutting in May or June decreased vegetative tillers, but increased crude protein content and in vitro dry digestibility [<xref ref-type="bibr" rid="scirp.81986-ref22">22</xref>] , autumn harvest date gained different quality forage [<xref ref-type="bibr" rid="scirp.81986-ref13">13</xref>] , winter cutting or grazing didn’t affect the spring ground or spring forage yield if it was accomplished before spring growth [<xref ref-type="bibr" rid="scirp.81986-ref23">23</xref>] . However, the time interval was always long, how different autumn relatively concentrated harvest dates effects on L. chinensis community in Songnen grassland had not been reported.</p><p>The objects of this study were: a) determining the cutting dates effecting on the regrowth at the end of the current year, b) assessing the effect of cutting dates on the grassland for the next year, c) seeking the optimal harvest dates of the grassland.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Study Site</title><p>Experiments were conducted on the cutting field at the Songnen Grassland Ecological Research Station, operated by Northeast Normal University and located at latitude 44˚40'N, longitude 123˚44'E, 150 km northwest of the provincial capital, PR Changchun, China. The study area has a frost-free period of about 140 days. The mean annual temperature ranges from 4.6˚C to 6.4˚C, varying from −16˚C in January to 25˚C in July. The annual precipitation is 350 - 450 mm and. The annual potential evapotranspiration is approximately three times as much as the mean annual precipitation. The main soil type of the area is a meadow chernozem with pH is 7.5 - 9.0 and organic matter is 3.5% - 6% in the surface layer. The grassland is continual cutting field and the dominant species is L. chinensis [<xref ref-type="bibr" rid="scirp.81986-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref17">17</xref>] .</p></sec><sec id="s2_2"><title>2.2. Experimental Design and Sampling Methods</title><p>The experiment was from the August 15<sup>th</sup>, 2006 to August 11<sup>th</sup>, 2007. The cutting date was from August 15<sup>th</sup> to October 4<sup>th</sup> in 2006 with every 10 days interval. The experiment used a randomized complete block design, the plots area were 5 m &#215; 5 m, 5 replications, and the height of the remaining stubble was about 5 cm using the reaphook. Then we investigated the regrowth character of the different treatments in October at the current year, including the regrowth plant height, leaf number, and aboveground biomass of L. chinensis, constitute of species, and density with the sampling area was 1 m &#215; 1 m in each plot.</p><p>We settled two 1 m &#215; 1 m subplots in each plot the on May 10<sup>th</sup> in next year after the grassland had been turning green. The first month we measured the length of the second leaf, the height of L. chinensis in each sample, and harvested the aboveground biomass of one of the two samples. We harvested the aboveground biomass of the other settled subplots on August 11<sup>th</sup>, 2007, measured the height of L. chinensis, the species composition of the plant community, the aboveground biomass of each species and the stem/leaf of L. chinensis. We also made the background investigation of the grassland on August 16<sup>th</sup>, 2006, the plots were 1 m &#215; 1 m with 10 replications.</p><p>The method of harvesting aboveground biomass was using the scissors to cut the plants getting closing to the ground. All the samples were oven-dried at 65˚C C for at least 48 hours immediately after harvest and weighted. The crude protein percentage was determined in duplicate using Kijldahl method (Kjeltec Analyzer Unit, FOSS TECATOR).</p></sec><sec id="s2_3"><title>2.3. Statistical Analysis</title><p>The similarity of community was calculated by S&#248;rensen Coefficient (IS<sub>s</sub> = 2C/(A+B), A and B are the number of the species of the two communities, C is the number of the common species) [<xref ref-type="bibr" rid="scirp.81986-ref24">24</xref>] . The effect of height, leaf number, leaf length, density, aboveground biomass and stem/leaf data were analyzed by ANOVA with Tukey test for multiple comparisons among the treatments. All statistical analyses were performed using SPSS 13.0 (SPSS Inc., Chicago, USA) at 0.05 level.</p></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Background Information at the Study Site</title><p>The species number of the community was few, and there were about nine species in 1 m<sup>2</sup>. The fresh and dry weight of L. chinensis made up 86.26% &#177; 2.25% and 89.70% &#177; 1.70% of the plant community aboveground biomass, the plant community fresh and dry weight were 517.17 &#177; 35.40 g/m<sup>2</sup> and 297.66 &#177; 18.99 g/m<sup>2</sup>, separately. The main companion species were Kalimeris integrifolia, Echinochloa crusgalli, Eragrostis pilosa, Setaria viridis, Lathyrus quinquenervius, Carex duriuscula, Scriprs fluriatilis, Eleocharis intersita, and Polygonum sibiricum. The height and density of L. chinensis were 31.47 &#177; 1.12 cm, and 1176 &#177; 66 plants/m<sup>2</sup>.</p></sec><sec id="s3_2"><title>3.2. Regrowth Character at the End in 2016</title><p>The values of regrowth character of L. chinensis descended as the cutting date putting off (<xref ref-type="table" rid="table1">Table 1</xref>). The height descended quickly after the first cutting date, which was 12.05 &#177; 0.52 cm. There were no significance between August 25<sup>th</sup> and September 4<sup>th</sup>, and between September 4<sup>th</sup> and September 14<sup>th</sup>, but there was significant difference between August 25<sup>th</sup> and September 4<sup>th</sup>. And the shortest height was at the last two cutting dates, September 4<sup>th</sup> and October 4<sup>th</sup>. The leaf number was significant different among the cutting dates (P &lt; 0.05). The cutting dates could be divided into three periods and there were significance in any two of the three periods. The regrowth density of L. chinensis was much less than that without cutting (1176 &#177; 66 plants/m<sup>2</sup>), the highest one was just litter more than half of that without cutting, the others were less and less, and L. chinensis density of the last cutting date just was as one fifth of that without cutting. The regrowth of the aboveground biomass were also light, and the heaviest was 18.44 &#177; 1.44 g/m<sup>2</sup> after the first cutting date.</p><p>The regrowth of other companion species were mainly K. integrifolia and C. duriuscula (<xref ref-type="table" rid="table2">Table 2</xref>). But the height of the species was short. The species such as Artemisia scoparia just appeared in some polts, and the cutting date on August 15<sup>th</sup> had the most regrowth species number.</p></sec><sec id="s3_3"><title>3.3. Turning Green Stage in the Second Year</title><p>The L. chinensis was at the third-leaf stage when we measured the plot on May 11<sup>th</sup>, 2007 after the grassland turning green, and we measured the second leaf length of L. chinensis (<xref ref-type="table" rid="table3">Table 3</xref>). The second leaf length were no significance among the first three cutting dates, there were significant difference on August 25<sup>th</sup>, September 14<sup>th</sup> and September 24<sup>th</sup>. And the trends were descending as the cutting dates delayed though most of them were not significant (<xref ref-type="table" rid="table3">Table 3</xref>).</p><p>The height of L. chinensis population was lowest on September 24<sup>th</sup>, but most of the treatments were not significant, the significant dates were between August 15<sup>th</sup>, August 25<sup>th</sup> and September 24<sup>th</sup> (<xref ref-type="table" rid="table3">Table 3</xref>).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> The regrowth character of L. chinensis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Date</th><th align="center" valign="middle" >Height (cm)</th><th align="center" valign="middle" >Leaf number</th><th align="center" valign="middle" >Density (plants/m<sup>2</sup>)</th><th align="center" valign="middle" >Biomass (g/m<sup>2</sup>)</th></tr></thead><tr><td align="center" valign="middle" >15 Aug</td><td align="center" valign="middle" >12.05 &#177; 0.52a</td><td align="center" valign="middle" >3.8 &#177; 0.12a</td><td align="center" valign="middle" >629.0 &#177; 49.04a</td><td align="center" valign="middle" >18.44 &#177; 1.44a</td></tr><tr><td align="center" valign="middle" >25 Aug</td><td align="center" valign="middle" >8.48 &#177; 0.47b</td><td align="center" valign="middle" >3.7 &#177; 0.06a</td><td align="center" valign="middle" >535.8 &#177; 42.75ab</td><td align="center" valign="middle" >14.28 &#177; 1.14b</td></tr><tr><td align="center" valign="middle" >4 Sep</td><td align="center" valign="middle" >7.22 &#177; 0.19bc</td><td align="center" valign="middle" >3.0 &#177; 0.08b</td><td align="center" valign="middle" >493.4 &#177; 57.85ab</td><td align="center" valign="middle" >5.12 &#177; 0.60c</td></tr><tr><td align="center" valign="middle" >14 Sep</td><td align="center" valign="middle" >6.34 &#177; 0.22c</td><td align="center" valign="middle" >2.6 &#177; 0.09b</td><td align="center" valign="middle" >409.0 &#177; 42.70bc</td><td align="center" valign="middle" >3.50 &#177; 0.37c</td></tr><tr><td align="center" valign="middle" >24 Sep</td><td align="center" valign="middle" >4.04 &#177; 0.30d</td><td align="center" valign="middle" >1.9 &#177; 0.14c</td><td align="center" valign="middle" >383.2 &#177; 33.72bc</td><td align="center" valign="middle" >2.94 &#177; 0.26c</td></tr><tr><td align="center" valign="middle" >4 Oct</td><td align="center" valign="middle" >4.01 &#177; 0.15d</td><td align="center" valign="middle" >1.7 &#177; 0.15c</td><td align="center" valign="middle" >236.4 &#177; 42.53c</td><td align="center" valign="middle" >1.71 &#177; 0.31c</td></tr></tbody></table></table-wrap><p>Means &#177; SE with different letters were significantly different at 0.05 level.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> The regrowth density of the species excluding L. chinensis</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Date</th><th align="center" valign="middle"  colspan="8"  >Species density (plants/m<sup>2</sup>)</th></tr></thead><tr><td align="center" valign="middle" >K. integrifolia</td><td align="center" valign="middle" >C. duriuscula</td><td align="center" valign="middle" >Artemisia scoparia</td><td align="center" valign="middle" >Ambiytropis muitiflora</td><td align="center" valign="middle" >Ixeris chinensis</td><td align="center" valign="middle" >L. quinquenervius</td><td align="center" valign="middle" >Potentilla flagellaris</td><td align="center" valign="middle" >P. sibiricum</td></tr><tr><td align="center" valign="middle" >15 Aug</td><td align="center" valign="middle" >53.6</td><td align="center" valign="middle" >70.8</td><td align="center" valign="middle" >0.4</td><td align="center" valign="middle" >0.4</td><td align="center" valign="middle" >4.2</td><td align="center" valign="middle" >2.6</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >--</td></tr><tr><td align="center" valign="middle" >25 Aug</td><td align="center" valign="middle" >37.6</td><td align="center" valign="middle" >75.2</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >--</td></tr><tr><td align="center" valign="middle" >4 Sep</td><td align="center" valign="middle" >40.4</td><td align="center" valign="middle" >82.4</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >7.6</td><td align="center" valign="middle" >0.4</td></tr><tr><td align="center" valign="middle" >14 Sep</td><td align="center" valign="middle" >29.0</td><td align="center" valign="middle" >45.8</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >0.4</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >14.6</td><td align="center" valign="middle" >0.2</td></tr><tr><td align="center" valign="middle" >24 Sep</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >53.0</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >3.0</td><td align="center" valign="middle" >--</td></tr><tr><td align="center" valign="middle" >4 Oct</td><td align="center" valign="middle" >1.0</td><td align="center" valign="middle" >88.0</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >--</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >0.2</td><td align="center" valign="middle" >2.2</td><td align="center" valign="middle" >--</td></tr></tbody></table></table-wrap><p>--: Meant that the species did not grow in the investigated plots.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> The turning green characteristic of L. chinensis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Date</th><th align="center" valign="middle" >Second leaf length (cm)</th><th align="center" valign="middle" >Height (cm)</th><th align="center" valign="middle" >Density (plants/m<sup>2</sup>)</th><th align="center" valign="middle" >Aboveground biomass (g/m<sup>2</sup>)</th></tr></thead><tr><td align="center" valign="middle" >15 Aug</td><td align="center" valign="middle" >6.92 &#177; 0.18ab</td><td align="center" valign="middle" >9.33 &#177; 0.14a</td><td align="center" valign="middle" >674.6 &#177; 68.6a</td><td align="center" valign="middle" >20.55 &#177; 2.57a</td></tr><tr><td align="center" valign="middle" >25 Aug</td><td align="center" valign="middle" >7.11 &#177; 0.21a</td><td align="center" valign="middle" >9.51 &#177; 0.19a</td><td align="center" valign="middle" >784.0 &#177; 91.4a</td><td align="center" valign="middle" >22.67 &#177; 1.67a</td></tr><tr><td align="center" valign="middle" >4 Sep</td><td align="center" valign="middle" >6.27 &#177; 0.22abc</td><td align="center" valign="middle" >8.60 &#177; 0.10ab</td><td align="center" valign="middle" >782.4 &#177; 84.0a</td><td align="center" valign="middle" >22.58 &#177; 3.45a</td></tr><tr><td align="center" valign="middle" >14 Sep</td><td align="center" valign="middle" >6.05 &#177; 0.28b</td><td align="center" valign="middle" >8.61 &#177; 0.32ab</td><td align="center" valign="middle" >908.8 &#177; 85.0a</td><td align="center" valign="middle" >22.54 &#177; 1.73a</td></tr><tr><td align="center" valign="middle" >24 Sep</td><td align="center" valign="middle" >5.86 &#177; 0.18c</td><td align="center" valign="middle" >8.26 &#177; 0.18b</td><td align="center" valign="middle" >911.4 &#177; 54.5a</td><td align="center" valign="middle" >25.16 &#177; 0.82a</td></tr><tr><td align="center" valign="middle" >4 Oct</td><td align="center" valign="middle" >6.19 &#177; 0.22abc</td><td align="center" valign="middle" >8.92 &#177; 0.32ab</td><td align="center" valign="middle" >806.4 &#177; 69.6a</td><td align="center" valign="middle" >27.33 &#177; 2.33a</td></tr></tbody></table></table-wrap><p>Means &#177; SE with different letters were significantly different at 0.05 level.</p><p>Neither the density nor aboveground biomass of L. chinensis were significance during the different cutting dates at the turning green stage (<xref ref-type="table" rid="table3">Table 3</xref>). The density of the first three cutting dates were less than the remaining treatments. The trend of aboveground biomass was ascending as the cutting date delayed. The maximum value was 27.33 &#177; 5.20 g/m<sup>2</sup> at the last cutting date.</p></sec><sec id="s3_4"><title>3.4. Harvesting Biomass at Middle August in the Second Year</title><p>The three indexes of L. chinensis population which we had measured were not significant among the different cutting dates at the harvest time (<xref ref-type="table" rid="table4">Table 4</xref>). The</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> The harvesting characteristic of L. chinensis population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Date</th><th align="center" valign="middle" >Height (cm)</th><th align="center" valign="middle" >Density (plants/m<sup>2</sup>)</th><th align="center" valign="middle" >Aboveground biomass (g/m<sup>2</sup>)</th></tr></thead><tr><td align="center" valign="middle" >15 Aug</td><td align="center" valign="middle" >24.71 &#177; 1.07a</td><td align="center" valign="middle" >992.8 &#177; 70.6a</td><td align="center" valign="middle" >174.34 &#177; 20.59a</td></tr><tr><td align="center" valign="middle" >25 Aug</td><td align="center" valign="middle" >26.05 &#177; 1.90a</td><td align="center" valign="middle" >1079.2 &#177; 55.9a</td><td align="center" valign="middle" >166.25 &#177; 11.03a</td></tr><tr><td align="center" valign="middle" >4 Sep</td><td align="center" valign="middle" >24.56 &#177; 1.24a</td><td align="center" valign="middle" >1208.4 &#177; 85.4a</td><td align="center" valign="middle" >177.23 &#177; 16.91a</td></tr><tr><td align="center" valign="middle" >14 Sep</td><td align="center" valign="middle" >25.19 &#177; 1.02a</td><td align="center" valign="middle" >1273.4 &#177; 130.4a</td><td align="center" valign="middle" >199.69 &#177; 18.20a</td></tr><tr><td align="center" valign="middle" >24 Sep</td><td align="center" valign="middle" >24.30 &#177; 2.20a</td><td align="center" valign="middle" >1355.4 &#177; 41.5a</td><td align="center" valign="middle" >192.20 &#177; 12.49a</td></tr><tr><td align="center" valign="middle" >4 Oct</td><td align="center" valign="middle" >29.70 &#177; 3.61a</td><td align="center" valign="middle" >1259.48 &#177; 56.5a</td><td align="center" valign="middle" >194.01 &#177; 26.15a</td></tr></tbody></table></table-wrap><p>Means &#177; SE: with different letters were significantly different at 0.05 level.</p><p>highest L. chinensis was on October 4. The character of the density was similar as the turning green stage (<xref ref-type="table" rid="table3">Table 3</xref>), the first three cutting dates were less than the remaining treatments. The maximum aboveground biomass was 199.69 &#177; 18.20 g/m<sup>2</sup> of the cutting on September 14<sup>th</sup>, and the minimum was 166.25 &#177; 11.03 g/m<sup>2</sup> of the cutting on August 25<sup>th</sup>.</p><p>The species number of the plant community were also few, the species saturation were 10, 9, 11, 12, 10 and 10, respectively for the cutting dates. The dominant species was L. chinensis, which made up the most proportion of the community both in density and aboveground biomass. The dry weight of L. chinensis contributed to at least 90% of the aboveground biomass (<xref ref-type="table" rid="table4">Table 4</xref>, <xref ref-type="fig" rid="fig2">Figure 2</xref>) .The main companion species were K. integrifolia, L. quinquenervius, C. duriuscula, E. intersita, P. sibiricum. But the aboveground biomass of L. chinensis community was not significant among the cutting dates, and they were about 200 g/m<sup>2</sup> (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>The coefficients of the community similarity (IS<sub>s</sub>) were high for the neighboring two cutting dates, and higher than 0.70. The highest coefficient was 0.84 between August 15<sup>th</sup> and August 25<sup>th</sup>, and, they 8 common species.</p><p>The values of stem/leaf of L. chinensis were not significant different during the cutting dates. And they all were lower than 0.70, so the weight of the leaves was 1.43 times as much as stems at least. And the cutting date on August 25<sup>th</sup>, the weight of the leaves was next to 2 times as much as stems. The crude protein was form 8.0% to 9.5%, but there was not significant among the treatments，the companion species contain higher crude protein than L. chinensis, which were from 10% to 12% (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><p>The Songnen grassland plays an important role in stock raising in northeast China because of its famous for producing L. chinensis which has high palatability and quality [<xref ref-type="bibr" rid="scirp.81986-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref17">17</xref>] . The species richness (species number) of the community is small, furthermore, the L. chinensis was absolute predominance (<xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig1">Figure 1</xref>). Therefore, the communities were extremely similarly with different cutting dates (<xref ref-type="table" rid="table5">Table 5</xref>). Mowing in succession years made the aboveground biomass and density descending, the percentage of the high quality herbage in the community decreasing, weeds increasing [<xref ref-type="bibr" rid="scirp.81986-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref26">26</xref>] . In our study, the values of height and aboveground biomass of L. chinensis had decreased from</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> The coefficient of the community similarity</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Treatments</th><th align="center" valign="middle" >15 Aug - 25 Aug</th><th align="center" valign="middle" >25 Aug - 4 Sep</th><th align="center" valign="middle" >4 Sep - 14 Sep</th><th align="center" valign="middle" >14 Sep - 24 Sep</th><th align="center" valign="middle" >24 Sep - 4 Oct</th></tr></thead><tr><td align="center" valign="middle" >IS<sub>s</sub></td><td align="center" valign="middle" >0.84</td><td align="center" valign="middle" >0.70</td><td align="center" valign="middle" >0.70</td><td align="center" valign="middle" >0.76</td><td align="center" valign="middle" >0.80</td></tr></tbody></table></table-wrap><p>2006 to 2007. But the L. chinensis proportion was improved after cutting, probably because the rainfall was less in 2007 than 2006, and L. chinensis is more tolerance than other species in the community [<xref ref-type="bibr" rid="scirp.81986-ref5">5</xref>] . The regrowth character also reflected the advantage of L. chinensis (<xref ref-type="table" rid="table1">Table 1</xref> and <xref ref-type="table" rid="table2">Table 2</xref>).</p><p>The value of stem/leaf was an important index of forage quality, intake, and diet selection [<xref ref-type="bibr" rid="scirp.81986-ref27">27</xref>] , usually the value was smaller and the nutrition was higher, because leaf contains more nutrition and is more palatable than stem [<xref ref-type="bibr" rid="scirp.81986-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref29">29</xref>] . The stem/leaf which we measured showed that there was no difference by the different treatments (<xref ref-type="fig" rid="fig2">Figure 2</xref>(a)), and the leaves made up a bigger percentage of the aboveground biomass and the quality was fine. And the crude protein percentage was also not significant both L. chinensis population and community, so we got the conclusion that autumn different cutting dates didn’t influence the quality of the L. chinensis grassland. But the plant community had more crude protein than L. chinensis population (<xref ref-type="fig" rid="fig2">Figure 2</xref>(b)), because the companion species contained more crude protein, especially the leguminous forage like L. quinquenervius [<xref ref-type="bibr" rid="scirp.81986-ref5">5</xref>] .</p><p>The aim of cutting in grassland was to gain hay or ensilage [<xref ref-type="bibr" rid="scirp.81986-ref30">30</xref>] , thus the harvesting date and forage yield were practical significance [<xref ref-type="bibr" rid="scirp.81986-ref11">11</xref>] . The aboveground biomass of L. chinensis population and community were not significant after different cutting dates (<xref ref-type="fig" rid="fig1">Figure 1</xref>), and the height, density and stem/leaf were also not significant. This meant that the concentrated harvest dates had the similar influence on the grassland at the remaining stubble was about 5 cm, so when farmers harvested the hay, they just need to consider the factors of weather, labor force, nutrition content and yield of the grassland. The aboveground biomass of L. chinensis reached hump at the middle ten days in August [<xref ref-type="bibr" rid="scirp.81986-ref9">9</xref>] , but the</p><p>crude protein decreased and fiber increased after L. chinensis turning green, in order to get maximum crude protein, the grassland should be cutting in the last ten days of July [<xref ref-type="bibr" rid="scirp.81986-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref14">14</xref>] . Considering the weather condition in Songnen grassland, we advised that harvest dates should be concentrated from the middle ten days of August to the first ten days in September [<xref ref-type="bibr" rid="scirp.81986-ref5">5</xref>] .</p><p>Cutting means removing the organics from the grassland [<xref ref-type="bibr" rid="scirp.81986-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.81986-ref31">31</xref>] , the utilization rate of the grassland was less than 50 percent to keep it healthy [<xref ref-type="bibr" rid="scirp.81986-ref25">25</xref>] , because plant litter played an important role on the grassland ecosystem [<xref ref-type="bibr" rid="scirp.81986-ref11">11</xref>] , and it alters the physical and chemical environment, therefore, it may affect the plant community structure and dynamics [<xref ref-type="bibr" rid="scirp.81986-ref32">32</xref>] . We also investigated the uncut community closed to the experimental plots in 2007, the height, aboveground biomass was significant more than the treatments because of the litter, and the stem/leaf and crude protein were not significant. However, the stand litter would be the obstacle when the farmers mow the grass and decrease the quality of the forage, so the managers need to trade-off the yield and quality, and institute the scientific cutting systems to keep the grassland continuative production.</p></sec></sec><sec id="s4"><title>4. Conclusion</title><p>The L. chinensis grassland produces herbage superior both in quality and in quantity on the Songnen plain of northeast China, and the L. chinensis makes up about 90% of the dry aboveground biomass in the L. chinensis community whose species richness is simple. The companion species of L. chinensis community contains higher crude protein, but the crude protein of the community is not significant. The coefficients of the community similarity are high. Furthermore the density, height, aboveground biomass, stem/leaf ratio, and crude protein of L. chinensis were not significant at the reviving stage and harvesting time. Thus, the harvest dates should be concentrated from the middle ten days of August to the first ten days in September when the weather is fine in this plain. The experiment showed one-year results, and longer-term research is required to get more reliable results.</p></sec><sec id="s5"><title>Acknowledgements</title><p>The National Science Foundation of China (31500366, 31470504), the Fundamental Research Funds for the Central Universities (No. DC201501070402). Prior Sci-Tech Programs of Overseas Chinese Talents Funds (2015).</p></sec><sec id="s6"><title>Cite this paper</title><p>Song, Y.T., Wuyunna and Zhou, D.W. (2018) Effect of Autumn Cutting Date on Regrowth, Turning Green, Yield and Quality of Leymus chinensis Grassland in Songnen Plain, Northeast China. 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