<?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.2018.92019</article-id><article-id pub-id-type="publisher-id">AJPS-81993</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>
 
 
  Volatiles from &lt;i&gt;Acer truncatum&lt;/i&gt; Flowers
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hongjian</surname><given-names>Ren</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>Fenfen</surname><given-names>Si</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>Meijing</surname><given-names>Ye</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>Qian</surname><given-names>Qiao</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>Kai</surname><given-names>An</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>Chao</surname><given-names>Wang</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>Zhen</surname><given-names>Feng</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>College of Horticulture Science and Engineering, Shandong Agricultural University, Tai’an, China</addr-line></aff><aff id="aff1"><addr-line>College of Forestry, Shandong Agricultural University, Tai’an, China</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>ren-hongjian@qq.com(HR)</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>231</fpage><lpage>238</lpage><history><date date-type="received"><day>13,</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>
 
 
  Plant volatile organic compounds (Biogenic Volatile Organic compounds, referred BVOCs) have a significant impact on the atmospheric environment, air quality and human health. This experiment takes 
  Acer truncatum
   flowers as 
  the research object, uses solid-phase micro-extraction combine GC-MS
   (SPME-GC-MS) to detect the main component of volatiles released by the flowers from 10 individual trees of 
  Acer truncatum
   (
  Acer truncatum
   Bunge). The results showed that 37 kinds of volatiles were detected and they are belonged to four types organic compouds, such as terpenoids, alcohols, ketones, esters. According to the analysis of the main components of 
  Acer truncatum
   flower volatiles includes Fluorene, 4,8 -Dimethyl-1,3 (E), 7-Nonene, (cis, trans)-2,6-Dimethyl-2,4,6-triene-Partenkirchen, Myrcene, Basil hexene, 3-Carene, (E)-
  Basil, Camphene, Caryophyllene, Linalool, α-Terpinolene, O-cymene
  , 3-Vinyl-1,2-dimethyl-1, 
  Eucalyptus 
  alcohols and Alcohol vinegar-12. However, there were no significant differences between individual trees in terms of obscure material O-cymene, 
  Eucalyptus 
  alcohols, Alcohol vinegar-12, as well as the significant differences in terms of remaining volatiles.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Acer truncatum&lt;/i&gt;</kwd><kwd> Flower</kwd><kwd> Volatiles</kwd><kwd> SPME</kwd><kwd> GC-MS</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>When the green plant absorbs CO<sub>2</sub> to release O<sub>2</sub>, it will synthesize low-boiling and volatile small molecular organic compounds, which is well known as plant volatile organic compounds (VOCs) [<xref ref-type="bibr" rid="scirp.81993-ref1">1</xref>] , with its secondary metabolic pathway. The discovery of its role in the ecosystem has attracted wide attention with further research [<xref ref-type="bibr" rid="scirp.81993-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.81993-ref3">3</xref>] . Plant VOCs contain the active ingredients have function about antibacterial, health care, air purification and so on. Extraction of some plant VOCs are widely used in food, medical care and health care etc. as the development of the aroma analysis technology and the close combination between various disciplines. Some VOCs can induce feelings of relaxation and comfort [<xref ref-type="bibr" rid="scirp.81993-ref4">4</xref>] and some aromatic VOCs have been reported to lower blood pressure and improve mood [<xref ref-type="bibr" rid="scirp.81993-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.81993-ref6">6</xref>] . Therefore, systematic investigation of plant volatile components, aimed at promotes the development of community ecology theory to make urban green system to play great role in urban ecological balance and sustainable development. Plant VOCs plays an important role in improving the quality of urban air and protecting citizen’s physical and mental health.</p><p>Acer truncatum Bunge, a member of the Aceracae family, is endemic to China, Korea and Japan but is also found in Europe and North America [<xref ref-type="bibr" rid="scirp.81993-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.81993-ref8">8</xref>] The genus Acer (Aceraceae), commonly known as maple, comprises approximately 129 species that primarily grow in the northern hemisphere, especially in the temperate regions of East Asia, eastern North America, and Europe [<xref ref-type="bibr" rid="scirp.81993-ref9">9</xref>] . There have been many phytochemical investigations focusing on Acer truncatum, as this species has great commercial value and numerous applications in traditional Chinese medicine and drinks production.</p><p>To date, 331 compounds have been identified from 34 species of the genus Acer, including flavonoids [<xref ref-type="bibr" rid="scirp.81993-ref10">10</xref>] , tannins, phenyl propanoids, diarylheptanoids, terpenoids, benzoic acid derivatives and several other types of compounds [<xref ref-type="bibr" rid="scirp.81993-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.81993-ref12">12</xref>] , such as phenylethanoid, glycosides and alkaloids [<xref ref-type="bibr" rid="scirp.81993-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.81993-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.81993-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.81993-ref16">16</xref>] . But no research has been conducted concerning the chemical constituents and pharmacological activities of Acer truncatum flowers. In order to identify the volatiles of Acer truncatum flowers, we report on their essential oils using the headspace solid-phase microextraction (HS-SPME) followed by GC-MS for the first time.</p><p>This research focuses on the development and utilization of this new type of resource―Acer truncatum flowers, which is based on the release of flower volatiles, and explores whether it could be exploited extensively in the aspects of environmental optimization or new resources development of traditional Chinese medicine.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Plant Materials</title><p>The flowers of Acer truncatum were collected from 10 individual trees at Mountain Taishan in Shandong Province, China, in March 2017. The sampled Acer truncatum tree was approximately 5.3 &#177; 1.2 m in height and 14.5 &#177; 1.7 cm in diameter at breast height (DBH). The trees No.8, No.9 and No.10 at the foot of the mountain and the remaining test materials, surrounded by more adequate sunshine, were all located in the valley. The branches with flowers facing the south were selected in the middle of the trees. The collected flower samples were deposited in the laboratory of College of Horticulture Science and Engineering, Shandong Agricultural University.</p></sec><sec id="s2_2"><title>2.2. Analysis of Volatile Compounds of the Flowers</title><p>Firstly, 1 g of fresh Acer truncatum flower was separately taken and weighed from different single plants, placed into 10 ml extraction glass bottle, sealed with aluminum foil, and separately marked. Then, the extraction was conducted at 40˚C using tips of 50/30 &#181;m DVB/CAR/PDMS (divinyl benzene/carbon molecular sieve/polydimethylsiloxane). The tips were then inserted into the injection port of a GC-MS and desorbed at 250˚C for 3 min. The GC oven was programmed for 2 min at 40˚C, followed by a temperature increase at the rate of 6˚C min<sup>−1</sup> to 90˚C, and then by an increase of 10˚C min<sup>−1</sup> to 200˚C, and finally by an increase of 15˚C min<sup>−1</sup> to 250˚C, where it was maintained for 5 min. The flow rate of He, carrier gas, was 1.0 m・L・min<sup>−1</sup>. The MS of the eluting compounds were generated at 80 eV, and recorded each second 45 - 450 m・z<sup>−1</sup>. The ion source was electron impact (EI), which has a temperature of 200˚C and interface temperature of 250˚C. The volatiles were identified by screening the NIST 08 and NIST 08 S libraries for comparable mass spectra and via comparison with authentic reference compounds. The relative percentages of the compounds were calculated using the areas of peak normalization method.</p></sec><sec id="s2_3"><title>2.3. Data Analysis</title><p>Statistical analyses were conducted using Excel 2007 for Windows and Statistical Program for the Social Sciences (SPSS 22.0) were used for a one-way analysis of variance(ANOVA), a Least Significant Difference (LSD) method was used for statistical evaluations, and the differences between the each treatment group were examined for significance at the 5% level(P &lt; 0.05).</p></sec></sec><sec id="s3"><title>3. Results</title><p>The volatiles of Acer truncatum flowers are presented in <xref ref-type="table" rid="table1">Table 1</xref>. Thirty-seven compounds were identified, which comprised by so many organic compounds. The type of volatile constituents of Acer truncatum flowers were abundant. The proportion of various volatiles was shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>. Terpenoids (85.23%) was the highest volutile constituent，followed by alcohols (3.05%), ketones (1.67%), esters (0.91%).</p><p>The most important discovery was that Fluorene was one of the representative key volatiles of Acer truncatum flowers. Its derivatives Fluorene as pharmaceutical intermediates used to produce anti-cancer drugs, antispasmodic agent, the sympathetic nerve inhibitors, blood pressure medications and antispasmodic drugs, as a pesticide intermediates, fluorenone could be used for the preparation of herbicides, fungicides, plant growth regulator, etc [<xref ref-type="bibr" rid="scirp.81993-ref17">17</xref>] . The demand for Fluorene has increased greatly in domestic and foreign markets, so it was becoming more and more important to study the extraction and refining methods of Fluorene. Some people have begun to study its refining work [<xref ref-type="bibr" rid="scirp.81993-ref18">18</xref>] .</p><table-wrap-group id="1"><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Components and relative contents of volatiles from flowers of Acer truncatum (mean &#177; SE)</title></caption><table-wrap id="1_1"><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Compound</th><th align="center" valign="middle"  colspan="10"  >Relative content/%</th><th align="center" valign="middle"  rowspan="2"  >Average content/%</th></tr></thead><tr><td align="center" valign="middle" >No.1</td><td align="center" valign="middle" >No.2</td><td align="center" valign="middle" >No.3</td><td align="center" valign="middle" >No.4</td><td align="center" valign="middle" >No.5</td><td align="center" valign="middle" >No.6</td><td align="center" valign="middle" >No.7</td><td align="center" valign="middle" >No.8</td><td align="center" valign="middle" >No.9</td><td align="center" valign="middle" >No.10</td></tr><tr><td align="center" valign="middle" >Fluorene</td><td align="center" valign="middle" >1.57 &#177; 0.087</td><td align="center" valign="middle" >4.48 &#177; 0.075</td><td align="center" valign="middle" >0.62 &#177; 0.144</td><td align="center" valign="middle" >0.57 &#177; 0.052</td><td align="center" valign="middle" >0.57 &#177; 0.053</td><td align="center" valign="middle" >0.42 &#177; 0.087</td><td align="center" valign="middle" >0.51 &#177; 0.231</td><td align="center" valign="middle" >0.46 &#177; 0.098</td><td align="center" valign="middle" >0.66 &#177; 0.098</td><td align="center" valign="middle" >0.51 &#177; 0.115</td><td align="center" valign="middle" >1.037</td></tr><tr><td align="center" valign="middle" >4,8 -Dimethyl -1,3 (E), 7-nonene</td><td align="center" valign="middle" >25.9 &#177; 0.481</td><td align="center" valign="middle" >68.8 &#177; 12.93</td><td align="center" valign="middle" >26.25 &#177; 0.563</td><td align="center" valign="middle" >6.18 &#177; 0.234</td><td align="center" valign="middle" >9.62 &#177; 0.334</td><td align="center" valign="middle" >26.6 &#177; 0.446</td><td align="center" valign="middle" >24.06 &#177; 0.583</td><td align="center" valign="middle" >26.82 &#177; 0.521</td><td align="center" valign="middle" >15.61 &#177; 0.36</td><td align="center" valign="middle" >7.39 &#177; 0.228</td><td align="center" valign="middle" >23.723</td></tr><tr><td align="center" valign="middle" >(cis, trans) -2,6-Dimethyl-2,4,6- triene-Partenkirchen</td><td align="center" valign="middle" >19.08 &#177; 0.332</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >13.54 &#177; 0.292</td><td align="center" valign="middle" >18.12 &#177; 0.267</td><td align="center" valign="middle" >20.41 &#177; 0.54</td><td align="center" valign="middle" >11.62 &#177; 0.600</td><td align="center" valign="middle" >15.12 &#177; 0.321</td><td align="center" valign="middle" >13.31 &#177; 1.145</td><td align="center" valign="middle" >8.44 &#177; 0.170</td><td align="center" valign="middle" >16.02 &#177; 0.362</td><td align="center" valign="middle" >13.566</td></tr><tr><td align="center" valign="middle" >Myrcene</td><td align="center" valign="middle" >0.33 &#177; 0.000</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.44 &#177; 0.087</td><td align="center" valign="middle" >0.85 &#177; 0.052</td><td align="center" valign="middle" >0.72 &#177; 0.092</td><td align="center" valign="middle" >0.73 &#177; 0.110</td><td align="center" valign="middle" >0.55 &#177; 0.064</td><td align="center" valign="middle" >0.59 &#177; 0.046</td><td align="center" valign="middle" >1.08 &#177; 0.162</td><td align="center" valign="middle" >1.17 &#177; 0.134</td><td align="center" valign="middle" >0.646</td></tr><tr><td align="center" valign="middle" >Ocimene</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >4.51 &#177; 0.548</td><td align="center" valign="middle" >0.48 &#177; 0.179</td><td align="center" valign="middle" >0.69 &#177; 0.173</td><td align="center" valign="middle" >0.81 &#177; 0.866</td><td align="center" valign="middle" >0.36 &#177; 0.635</td><td align="center" valign="middle" >0.55 &#177; 0.04</td><td align="center" valign="middle" >0.51 &#177; 0.104</td><td align="center" valign="middle" >0.45 &#177; 0.751</td><td align="center" valign="middle" >0.89 &#177; 0.751</td><td align="center" valign="middle" >0.0925</td></tr><tr><td align="center" valign="middle" >3-Carene</td><td align="center" valign="middle" >39.85 &#177; 0.440</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >40.74 &#177; 0.321</td><td align="center" valign="middle" >50.16 &#177; 0.416</td><td align="center" valign="middle" >51.2 &#177; 0.655</td><td align="center" valign="middle" >31.04 &#177; 0.621</td><td align="center" valign="middle" >44.54 &#177; 0.616</td><td align="center" valign="middle" >40.94 &#177; 0.688</td><td align="center" valign="middle" >43.12 &#177; 0.95</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >34.159</td></tr><tr><td align="center" valign="middle" >(E)-Ocimene</td><td align="center" valign="middle" >1.79 &#177; 0.043</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >3.32 &#177; 0.140</td><td align="center" valign="middle" >3.27 &#177; 0.035</td><td align="center" valign="middle" >2.13 &#177; 0.103</td><td align="center" valign="middle" >2.46 &#177; 0.052</td><td align="center" valign="middle" >2.5 &#177; 0.072</td><td align="center" valign="middle" >2.23 &#177; 0.148</td><td align="center" valign="middle" >4.43 &#177; 0.101</td><td align="center" valign="middle" >2.213</td></tr><tr><td align="center" valign="middle" >Camphene</td><td align="center" valign="middle" >1.77 &#177; 0.000</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.42 &#177; 0.058</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.17 &#177; 0.035</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.69 &#177; 0.069</td><td align="center" valign="middle" >7.58 &#177; 0.606</td><td align="center" valign="middle" >0.38 &#177; 0.046</td><td align="center" valign="middle" >1.01</td></tr><tr><td align="center" valign="middle" >Caryophyllene</td><td align="center" valign="middle" >2.73 &#177; 0.000</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.2 &#177; 0.121</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >5.69 &#177; 0.185</td><td align="center" valign="middle" >1.42 &#177; 0.133</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.51 &#177; 0.395</td><td align="center" valign="middle" >0.87 &#177; 0.087</td><td align="center" valign="middle" >1.442</td></tr><tr><td align="center" valign="middle" >Linalool</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >4.01 &#177; 0.127</td><td align="center" valign="middle" >9.7 &#177; 0.191</td><td align="center" valign="middle" >1 &#177; 0.075</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.46 &#177; 0.202</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2 &#177; 0.318</td><td align="center" valign="middle" >1.917</td></tr><tr><td align="center" valign="middle" >3-Vinyl-1,2-dimethyl-1</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.63 &#177; 0.225</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.37 &#177; 0.121</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.9 &#177; 0.133</td><td align="center" valign="middle" >2.26 &#177; 0.098</td><td align="center" valign="middle" >3.51 &#177; 0.087</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.167</td></tr><tr><td align="center" valign="middle" >α-Terpinolene</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.46 &#177; 0.040</td><td align="center" valign="middle" >0.58 &#177; 0.040</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.51 &#177; 0.092</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.44 &#177; 0.115</td><td align="center" valign="middle" >0.299</td></tr><tr><td align="center" valign="middle" >1-Isopropyl-2-methylbenzene</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" >0.66 &#177; 0.038</td><td align="center" valign="middle" >0.42 &#177; 0.036</td><td align="center" valign="middle" >0.62 &#177; 0.026</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.54 &#177; 0.040</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.224</td></tr><tr><td align="center" valign="middle" >1,3-Pentadiene, 4-methyl-</td><td align="center" valign="middle" >0.45</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" >0.19</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.43</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.107</td></tr><tr><td align="center" valign="middle" >Cosmene</td><td align="center" valign="middle" >1.29</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.55</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.57</td><td align="center" valign="middle" >0.241</td></tr><tr><td align="center" valign="middle" >Eucalyptus alcohols</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.46 &#177; 0.029</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" >0.21 &#177; 0.058</td><td align="center" valign="middle" >0.26 &#177; 0.040</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.093</td></tr><tr><td align="center" valign="middle" >Matrine</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.55</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >2.25</td><td align="center" valign="middle" >0.280</td></tr><tr><td align="center" valign="middle" >Alcohol vinegar-12</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.24</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.32</td><td align="center" valign="middle" >0.16</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.072</td></tr><tr><td align="center" valign="middle" >Alpha-Pinene</td><td align="center" valign="middle" >0.35</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.12</td><td align="center" valign="middle" >0.047</td></tr><tr><td align="center" valign="middle" >Aaromatic alcohol</td><td align="center" valign="middle" >4.11</td><td align="center" valign="middle" >3.75</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.786</td></tr><tr><td align="center" valign="middle" >Cis-jasmone</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" >0.38</td><td align="center" valign="middle" >0.17</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" >0.055</td></tr><tr><td align="center" valign="middle" >1-Acenaphthenone</td><td align="center" valign="middle" >0.65</td><td align="center" valign="middle" >2.07</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.272</td></tr><tr><td align="center" valign="middle" >Alloaeromadendrene</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >5.5</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.52</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.602</td></tr><tr><td align="center" valign="middle" >2,6-Dimethyloctane-1,3,5,7-tetraene</td><td align="center" valign="middle" >-</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" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.59</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.098</td></tr><tr><td align="center" valign="middle" >Dihydrocarveol</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.45</td><td align="center" valign="middle" >0.58</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.023</td></tr><tr><td align="center" valign="middle" >2,5-Dimethyl-3-methylene-1,5-heptadiene</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.01</td><td align="center" valign="middle" >1.17</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.218</td></tr><tr><td align="center" valign="middle" >Trans-hex-3-en-1-ol</td><td align="center" valign="middle" >0.58</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.058</td></tr></tbody></table></table-wrap><table-wrap id="1_2"><table><tbody><thead><tr><th align="center" valign="middle" >Cis-3-hexenyl acetate</th><th align="center" valign="middle" >3.42</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >-</th><th align="center" valign="middle" >0.342</th></tr></thead><tr><td align="center" valign="middle" >Hexyl acetate</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" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.04</td></tr><tr><td align="center" valign="middle" >Butyric acid</td><td align="center" valign="middle" >0.49</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.049</td></tr><tr><td align="center" valign="middle" >Piperonyl alcohol</td><td align="center" valign="middle" >1.13</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.113</td></tr><tr><td align="center" valign="middle" >1,2,4-Methyl azulene</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.27</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.027</td></tr><tr><td align="center" valign="middle" >2-Furfuryl alcohol</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.55</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.055</td></tr><tr><td align="center" valign="middle" >Benzene</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >1.52</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.152</td></tr><tr><td align="center" valign="middle" >Safranal</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.23</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" >0.023</td></tr><tr><td align="center" valign="middle" >4-Isopropyltoluene</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.8</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.08</td></tr><tr><td align="center" valign="middle" >3,7-Dimethyl 1,3,6 octadecadiene</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >55.31</td><td align="center" valign="middle" >5.531</td></tr></tbody></table></table-wrap></table-wrap-group><p>Recent research showed that 3-Carene had sedative and analgesic, digestion and analgesic, antimicrobial effects. [<xref ref-type="bibr" rid="scirp.81993-ref19">19</xref>] Sinem Milanos [<xref ref-type="bibr" rid="scirp.81993-ref20">20</xref>] on the metabolism of Linalool and Linalool the regulation process has been studied and the results confirm that Linalool is well-known for its calming effect in the field of medicine. β-Pinene has obvious antibacterial activity in vitro [<xref ref-type="bibr" rid="scirp.81993-ref21">21</xref>] , and Caryophyllene also has strong bacteriostatic action [<xref ref-type="bibr" rid="scirp.81993-ref22">22</xref>] .</p></sec><sec id="s4"><title>4. Discussion</title><p>Plant volatile organic compounds (Biogenic Volatile Organic compounds, referred BVOCs) have significant impact on the atmospheric environment, air quality and human health. Different VOCs from different plants have positive or negative impact on the circulatory system, and different human gender responded differently, for example Roger Atkinson et al. [<xref ref-type="bibr" rid="scirp.81993-ref23">23</xref>] introduced so many species and of selected classes of volatile organic compounds (VOCs), include alkanes, alkenes, aromatic hydrocarbons. Kikuchi et al. [<xref ref-type="bibr" rid="scirp.81993-ref24">24</xref>] found that Rosa rugosa aroma caused an increase in heart rate while Citrus limonum aroma had a calming effect and caused a reduction in heart rate. These VOCs could improve the respiratory and circulatory system according to the data.</p><p>There are several studies on the volatile compounds of Acer. For example, the main volatile compounds from Acer truncatum leaves included 3-hexen-1-ol acetate, 3-hexen-1-ol, acetic acid hexyl ester [<xref ref-type="bibr" rid="scirp.81993-ref25">25</xref>] . However, the main volatile compounds from Acer oliverianum leaves were terpenoids [<xref ref-type="bibr" rid="scirp.81993-ref26">26</xref>] . This is the firstly research of flower volatiles from Aceracae family.</p><p>Acer truncatum is an important species in Aceracae family. The leaves of Acer truncatum contain flavonoids, organic acids, proteins, polysaccharides and tannins [<xref ref-type="bibr" rid="scirp.81993-ref27">27</xref>] . They are widely applied in many fields, such as medical, food and chemical industry. Acer truncatum comprehensive application value was very high, but previous studies have focused on the leaf and fruit. The study on the chemical constituents from flowers of Acer truncatum has not been reported, this study reveals the kinds of volatiles of Acer truncatum flower contains most of the ingredients, pharmacological activity significantly, with further development and application potential.</p></sec><sec id="s5"><title>5. Conclusions</title><p>The kinds of the volatiles of Acer truncatum flower are rich. 37 kinds of volatile components were detected, the main ingredient includes Fluorene, 4,8-Dimethyl- 1,3 (E), 7-Nonene, (cis, trans)-2,6-Dimethyl-2,4,6-triene-Partenkirchen, Myrcene, Basil hexene, 3-Carene, (E)-Basil, Camphene, Caryophyllene, Linalool, α-Ter- pinolene, O-cymene, 3-Vinyl-1,2-dimethyl-1, Eucalyptus alcohols, Alcohol vinegar-12. However, there were no significant differences between individual trees in terms of O-cymene, Eucalyptus alcohols, Alcohol vinegar-12 and the significant differences in terms of the remaining volatiles. Furthermore, the representative substance of ketone plants, Fluorene is the first discovery of key volatiles from Acer truncatum flowers. Fluorene can be used in making medicine such as antispasmodic, sedatives, analgesic, and antihypertensive drugs. Therefore, the flowers of Acer truncatum may be new natural resources for pharmaceutical manufacturing.</p><p>This research not only provides theoretical and technical guidance for creating eco-healthy urban green space, but also lays a scientific foundation for the development and utilization of Acer truncatum scented tea and new resources of traditional Chinese medicine.</p></sec><sec id="s6"><title>Acknowledgements</title><p>Thanks to the Shandong Agricultural Seeds Engineering Project, Improvement and Demonstration of New Varieties with High Quality and High Yield for Medicinal Trees―Acer truncatum (2016LZGC014) and the Funds of Shandong “Double Tops” Program for financial support.</p></sec><sec id="s7"><title>Cite this paper</title><p>Ren, H.J., Si, F.F., Ye, M.J., Qiao, Q., An, K., Wang, C. and Feng, Z. (2018) Volatiles from Acer truncatum Flowers. 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