Difference between revisions of "User:Shawndouglas/Sandbox"

From CannaQAWiki
Jump to navigationJump to search
Line 1,695: Line 1,695:
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Monoterpene hydrocarbons
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Monoterpene hydrocarbons
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|4.3 ± 0.71 BCD;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|4.3 ± 0.71<sup>BCD;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|4.1 ± 1.57 BCD;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|4.1 ± 1.57<sup>BCD;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.8 ± 0.52 DE;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.8 ± 0.52<sup>DE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.0 ± 0.36 DE;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.0 ± 0.36<sup>DE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|4.0 ± 0.60 BCD;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|4.0 ± 0.60<sup>BCD;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.2 ± 0.15 E;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.2 ± 0.15<sup>E;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|7.5 ± 0.42 A;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|7.5 ± 0.42<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|5.7 ± 2.07 AB;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|5.7 ± 2.07<sup>AB;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|3.7 ± 0.01 BCDE;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|3.7 ± 0.01<sup>BCDE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.5 ± 0.85 CDE;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.5 ± 0.85<sup>CDE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|4.7 ± 0.35 BC;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|4.7 ± 0.35<sup>BC;a</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Oxygenated monoterpenes
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Oxygenated monoterpenes
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.5 ± 0.10 DE;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.5 ± 0.10<sup>DE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.9 ± 0.34 D;b
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.9 ± 0.34<sup>D;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.3 ± 0.06 E;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.3 ± 0.06<sup>E;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.2 ± 0.05 E;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.2 ± 0.05<sup>E;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.5 ± 0.07 DE;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.5 ± 0.07<sup>DE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.9 ± 0.15 D;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.9 ± 0.15<sup>D;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.8 ± 0.20 BC;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.8 ± 0.20<sup>BC;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.3 ± 0.30 A;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.3 ± 0.30<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.4 ± 0.12 C;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.4 ± 0.12<sup>C;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.6 ± 0.06 DE;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.6 ± 0.06<sup>DE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.0 ± 0.10 AB;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.0 ± 0.10<sup>AB;a</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Sesquiterpene hydrocarbons
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Sesquiterpene hydrocarbons
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|35.5 ± 2.88 A;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|35.5 ± 2.88<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|35.6 ± 2.00 A;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|35.6 ± 2.00<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|29.6 ± 6.37 AB;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|29.6 ± 6.37<sup>AB;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|35.8 ± 3.03 A;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|35.8 ± 3.03<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|21.3 ± 0.88 B,a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|21.3 ± 0.88<sup>B,a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|29.7 ± 3.84 AB;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|29.7 ± 3.84<sup>AB;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|28.5 ± 1.67 AB;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|28.5 ± 1.67<sup>AB;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|31.8 ± 3.45 AB;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|31.8 ± 3.45<sup>AB;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|34.5 ± 2.15 A;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|34.5 ± 2.15<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|36.9 ± 8.42 A;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|36.9 ± 8.42<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|29.6 ± 1.31 AB;a
   | style="background-color:white; padding-left:10px; padding-right:10px;"|29.6 ± 1.31<sup>AB;a</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Oxygenated sesquiterpenes
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Oxygenated sesquiterpenes
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|28.2 ± 2.24<sup>CD;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|33.1 ± 4.36<sup>BC;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|33.2 ± 7.07<sup>BC;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|35.6 ± 1.25<sup>BC;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|50.3 ± 0.95<sup>A;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|40.3 ± 4.64<sup>B;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|18.6 ± 2.13<sup>E;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|22.9 ± 1.59<sup>DE;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|30.9 ± 0.22<sup>CD;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|32.3 ± 2.09<sup>BC;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|22.9 ± 0.47<sup>DE;b</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Diterpene hydrocarbons
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Diterpene hydrocarbons
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.4 ± 0.11<sup>BC;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.06<sup>D;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.9 ± 0.14<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.5 ± 0.08<sup>B;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>D</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.02<sup>CD;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.0 ± 0.19<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.8 ± 0.12<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.01<sup>CD;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>D</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.9 ± 0.00<sup>A;a</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Oxygenated diterpenes
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Oxygenated diterpenes
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
  | style="background-color:white; padding-left:10px; padding-right:10px;"|0.5 ± 0.14<sup>CD;b</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|0.4 ± 0.18<sup>D;b</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|0.8 ± 0.27<sup>BCD;b</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|0.4 ± 0.05<sup>D;b</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|3.2 ± 0.11<sup>A;a</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|2.7 ± 0.04<sup>A;b</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|0.9 ± 0.06<sup>BC;a</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|0.7 ± 0.19<sup>BCD;b</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|1.0 ± 0.07<sup>B;b</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|0.8 ± 0.23<sup>BCD;a</sup>
  | style="background-color:white; padding-left:10px; padding-right:10px;"|0.9 ± 0.11<sup>BC;a</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Phenylpropanoids
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Phenylpropanoids
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.2 ± 0.06<sup>AB;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.07<sup>CD;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>D</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.03<sup>BC;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.3 ± 0.01<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>D</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>D</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>D</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>D</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.2 ± 0.07<sup>AB;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>D</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Cannabinoids
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Cannabinoids
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|24.2 ± 6.57<sup>BCDE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|22.8 ± 0.94<sup>BCDE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|29.1 ± 1.61<sup>ABCD;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|21.8 ± 4.21<sup>CDE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|17.4 ± 0.47<sup>DE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|15.0 ± 1.45<sup>E;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|37.7 ± 5.23<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|31.3 ± 2.45<sup>ABC;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|23.3 ± 2.80<sup>BCDE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|22.1 ± 10.63<sup>CDE;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|35.5 ± 0.91<sup>AB;a</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Apocarotenoids
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Apocarotenoids
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.6 ± 0.11<sup>C;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.6 ± 0.15<sup>C;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.4 ± 0.38<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.0 ± 0.21<sup>C;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.5 ± 0.13<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|2.5 ± 0.06<sup>A;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.8 ± 0.14<sup>C;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|1.5 ± 0.05<sup>B;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.7 ± 0.03<sup>C;b</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.8 ± 0.14<sup>C;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.7 ± 0.01<sup>C;b</sup>
  |-
  |-
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Other non-terpene derivatives
   | style="background-color:white; padding-left:10px; padding-right:10px;"|Other non-terpene derivatives
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.07<sup>B;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>B</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.07<sup>B;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>B</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.08<sup>B;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.4 ± 0.10<sup>A;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.10<sup>B;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.2 ± 0.11<sup>B;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.12<sup>B;a</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|-<sup>B</sup>
   | style="background-color:white; padding-left:10px; padding-right:10px;"|
   | style="background-color:white; padding-left:10px; padding-right:10px;"|0.1 ± 0.12<sup>B;a</sup>
  |-
  |-
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|'''Extraction yield (% ''w/w'')'''
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|'''Extraction yield (% ''w/w'')'''
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.12 ± 0.01<sup>CD;a</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.23 ± 0.02<sup>A;a</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.12 ± 0.00<sup>CD;a</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.17 ± 0.01<sup>ABC;a</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.03 ± 0.00<sup>E</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.05 ± 0.01<sup>DE;a</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.13 ± 0.00<sup>DE;a</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.20 ± 0.02<sup>AB;a</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.20 ± 0.00<sup>AB</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.14 ± 0.04<sup>BC;a</sup>
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|
   | style="background-color:#eeeeee; padding-left:10px; padding-right:10px;"|0.16 ± 0.01<sup>ABC;a</sup>
  |-
  |-
|}
|}
|}
|}

Revision as of 18:10, 27 July 2021

Using FontAwesome: <i class="fa fa-name-of-file"></i>

FontAwesome icons (click on one to get the file name): http://fontawesome.io/icons/

Making movies

Level one

Video capture

Level two

The technology

Level three

Using Bluetooth

Level four


Efnndng

Table 3. Complete composition and extraction yield (% w/w dry weight) of the essential oil obtained from the dried inflorescences and floral bracts of 2020 hemp samples.
 
1 LRI = Linear retention index on a HP 5-MS capillary column; 2 Not detected; 3 Compounds accounting for at least 1.000% of the dissimilarity rate (according to the SIMPER test; see Table 4) are evidenced in bold. For these compounds, for all chemical classes, and for the extraction yield, different superscript uppercase letters (AG) indicate statistically significant differences between each variety; superscript lowercase letters (a,b) indicate statistically significant differences among the cultivar withdrawn on different years (see Table 2 for 2019 samples). The statistical significance of the relative abundances was established by the Tukey’s post-hoc test, with p ≤ 0.05.
Relative abundance (%) ± SD
Compounds LRI1 Monoecious Dioecious
Carmaleonte Codimono Felina 32 Futura 75 Uso-31 Bernabeo Carmagnola CS Eletta Campana Fibranova Fibrante
heptanal 901 -2 - - - - 0.3 ± 0.06 0.1 ± 0.10 0.1 ± 0.04 0.1 ± 0.07 - -
α-pinene3 933 2.7 ± 0.50AB;a 2.0 ± 0.74ABC;a 1.1 ± 0.40CD;a 1.1 ± 0.11CD;a 2.0 ± 0.26ABC;a 0.5 ± 0.06D;a 3.0 ± 0.04A;a 2.1 ± 0.79ABC;a 1.7 ± 0.01BC;a 1.3 ± 0.39CD;a 1.2 ± 0.06CD;a
β-pinene 977 0.5 ± 0.06 0.5 ± 0.17 0.3 ± 0.07 0.2 ± 0.06 0.7 ± 0.18 0.1 ± 0.01 0.8 ± 0.09 0.7 ± 0.26 0.5 ± 0.02 0.3 ± 0.12 0.4 ± 0.03
myrcene3 991 0.8 ± 0.09CD;a 0.8 ± 0.33CD;a 0.2 ± 0.02D;a 0.4 ± 0.09D;a 0.6 ± 0.12D;a 0.4 ± 0.05D;a 2.6 ± 0.16A;a 1.3 ± 0.49BC;a 0.6 ± 0.01D;a 0.3 ± 0.10D;a 1.8 ± 0.17B;a
δ-3-carene 1011 0.1 ± 0.05 - - - - - - - 0.1 ± 0.01 0.3 ± 0.09 -
α-terpinene 1017 - - - - - - - 0.1 ± 0.06 - - -
limonene 1029 0.1 ± 0.01 0.1 ± 0.08 - - 0.2 ± 0.01 0.1 ± 0.03 0.6 ± 0.10 0.7 ± 0.16 0.4 ± 0.01 0.1 ± 0.08 0.8 ± 0.08
1,8-cineole 1031 - 0.2 ± 0.05 - - - 0.2 ± 0.05 0.2 ± 0.09 0.2 ± 0.06 0.1 ± 0.02 0.2 ± 0.06 0.1 ± 0.06
(E)-β-ocimene 1047 0.1 ± 0.01 0.4 ± 0.13 - 0.1 ± 0.03 0.4 ± 0.02 - 0.3 ± 0.02 0.1 ± 0.06 0.2 ± 0.01 0.3 ± 0.07 -
γ-terpinene 1058 - - - - - - - 0.1 ± 0.07 - - -
terpinolene 1089 - 0.4 ± 0.14 0.2 ± 0.04 0.1 ± 0.09 0.1 ± 0.02 0.1 ± 0.01 0.3 ± 0.03 0.8 ± 0.19 0.3 ± 0.01 - 0.5 ± 0.03
nonanal 1105 0.1 ± 0.07 - - - 0.1 ± 0.06 0.2 ± 0.04 - - - - -
linalool 1101 - 0.1 ± 0.06 - - - - 0.2 ± 0.01 0.2 ± 0.04 0.1 ± 0.03 - -
fenchol 1114 - - - - - - 0.2 ± 0.02 0.4 ± 0.07 0.2 ± 0.05 - 0.3 ± 0.00
cis-p-menth-2-en-1-ol 1122 - - - - - - 0.2 ± 0.02 0.2 ± 0.03 0.2 ± 0.02 - 0.2 ± 0.01
trans-pinocarveol 1139 0.3 ± 0.03 - - - 0.1 ± 0.01 - - - - - -
trans-verbenol 1145 - - - - 0.2 ± 0.01 - - - - - -
ipsdienol 1147
β-pinene oxide 1156 - - - - - - 0.3 ± 0.03 - - - 0.1 ± 0.01
borneol 1165 0.2 ± 0.02 0.1 ± 0.05 - - - 0.1 ± 0.00 0.2 ± 0.02 0.2 ± 0.04 0.2 ± 0.00 0.1 ± 0.06 0.2 ± 0.01
lavandulol 1170 - 0.4 ± 0.09 0.3 ± 0.06 0.2 ± 0.05 0.2 ± 0.05 0.4 ± 0.06 0.3 ± 0.01 0.6 ± 0.03 0.3 ± 0.01 - 0.6 ± 0.04
4-terpineol 1177 - - - - - - - - - 0.2 ± 0.03 -
p-cymen-8-ol 1185 - - - - - - - - - - -
myrtenal 1194 - - - - - - - - - - -
α-terpineol 1191 - 0.2 ± 0.03 - - - 0.2 ± 0.04 0.3 ± 0.01 0.5 ± 0.04 - 0.2 ± 0.03 0.5 ± 0.02
eugenol 1357 0.2 ± 0.06 0.1 ± 0.07 - 0.1 ± 0.03 0.1 ± 0.01 - - - - 0.2 ± 0.07 -
methyl eugenol 1405 - - - - 0.1 ± 0.02 - - - - - -
α-ylangene 1374 0.2 ± 0.01 0.1 ± 0.07 - 0.1 ± 0.01 - - 0.1 ± 0.04 0.1 ± 0.02 0.3 ± 0.01 0.1 ± 0.07 -
isocaryophyllene 1407 0.4 ± 0.03 0.4 ± 0.00 0.3 ± 0.09 0.4 ± 0.03 0.2 ± 0.01 0.3 ± 0.11 0.2 ± 0.04 0.3 ± 0.06 0.3 ± 0.01 0.5 ± 0.12 0.3 ± 0.01
cis-α-bergamotene 1416 - 0.1 ± 0.01 0.4 ± 0.14 0.1 ± 0.09 - - - - - - -
β-caryophyllene3 1419 15.3 ± 1.44AB;a 16.2 ± 1.46AB;a 11.5 ± 3.55ABC;a 13.8 ± 0.59ABC;a 8.7 ± 0.77C;a 10.4 ± 2.95BC;a 14.4 ± 0.89ABC;a 15.4 ± 2.45AB;a 11.6 ± 0.09ABC;a 16.8 ± 3.82A;a 16.2 ± 0.8AB;a
trans-α-bergamotene 1436 0.3 ± 0.00 1.1 ± 0.04 1.6 ± 0.42 1.5 ± 0.16 1.0 ± 0.06 0.3 ± 0.06 0.1 ± 0.01 0.1 ± 0.08 0.3 ± 0.01 0.9 ± 0.2 -
α-guaiene 1439 - - - - - 0.6 ± 0.14 - - - - -
aromadendrene 1142 - - - - - - - - - 0.3 ± 0.04 -
guaia-6,9-diene 1443 0.2 ± 0.01 - - - - - - - 0.1 ± 0.05 0.1 ± 0.05 -
isogermacrene D 1451 0.3 ± 0.03 - - - - - - - 0.2 ± 0.01 - -
α-humulene3 1453 6.9 ± 1.00ABC;a 7.6 ± 0.17A;a 4.7 ± 1.23DE;a 5.8 ± 0.38ABCDE;a 4.1 ± 0.06E;a 6.2 ± 0.27ABCD;a 5.3 ± 0.10CDE;a 7.5 ± 0.19A;a 5.4 ± 0.13BCDE;a 6.3 ± 1.44ABCD;a 7.4 ± 0.38AB;a
aristolene 1452 - - - 0.1 ± 0.05 - - - - - - -
(E)-β-farnesene 1458 0.3 ± 0.04 1.2 ± 0.07 1.4 ± 0.37 1.7 ± 0.19 1.1 ± 0.05 0.4 ± 0.01 0.1 ± 0.07 0.1 ± 0.09 0.3 ± 0.03 0.8 ± 0.19 0.1 ± 0.06
alloaromadendrene 1460 0.4 ± 0.07 0.9 ± 0.00 0.6 ± 0.16 0.7 ± 0.07 0.9 ± 0.01 0.4 ± 0.03 0.3 ± 0.03 0.5 ± 0.01 0.4 ± 0.02 0.5 ± 0.09 0.2 ± 0.01
4,5-di-epi-aristolochene 1468 - - - - - - - - - - -
γ-gurjunene 1469 - - - - - - - - - - -
β-chamigrene 1476 - - - 0.1 ± 0.07 - 0.1 ± 0.03 - - - - -
γ-muurolene 1477 0.3 ± 0.02 - 0.2 ± 0.05 0.2 ± 0.04 - 0.1 ± 0.01 - - 0.4 ± 0.09 0.2 ± 0.04 -
α-amorphene 1482 0.2 ± 0.02 0.2 ± 0.01 0.1 ± 0.02 0.2 ± 0.04 - 0.2 ± 0.01 0.1 ± 0.01 0.1 ± 0.01 0.1 ± 0.03 0.1 ± 0.03 -
γ-selinene 1483 0.5 ± 0.01 0.6 ± 0.04 0.5 ± 0.11 0.6 ± 0.10 0.4 ± 0.01 0.6 ± 0.01 0.5 ± 0.02 0.5 ± 0.03 0.5 ± 0.04 0.5 ± 0.11 0.4 ± 0.01
β-selinene3 1486 1.3 ± 0.03CDE;a 1.5 ± 0.10CDE;a 2.1 ± 0.48AB;a 2.2 ± 0.30A;a 1.9 ± 0.02ABC;a 1.5 ± 0.08BCDE;a 1.2 ± 0.07E;a 1.4 ± 0.13CDE;a 1.8 ± 0.09ABCD;a 1.3 ± 0.31CDE;a 1.3 ± 0.05DE;a
δ-selinene 1491 0.2 ± 0.01 0.1 ± 0.01 - 0.2 ± 0.04 - 0.3 ± 0.03 0.2 ± 0.02 0.2 ± 0.01 0.1 ± 0.04 0.1 ± 0.06 0.1 ± 0.05
valencene 1493 0.3 ± 0.01 0.3 ± 0.03 0.2 ± 0.05 0.3 ± 0.04 0.2 ± 0.00 0.3 ± 0.02 0.3 ± 0.05 0.3 ± 0.02 0.2 ± 0.00 0.3 ± 0.06 0.2 ± 0.02
α-selinene 1495 1.2 ± 0.00 1.2 ± 0.04 1.7 ± 0.40 1.5 ± 0.20 0.9 ± 0.09 1.5 ± 0.06 1.0 ±0.20 1.1 ±0.07 1.5 ± 0.16 1.0 ± 0.26 1.0 ± 0.07
eremophilene 1499 - - - - - - - 0.1 ± 0.04 - - -
α-bulnesene 1505 - - - 0.1 ± 0.02 - 1.4 ± 0.04 0.2 ± 0.05 - 0.1 ± 0.03 0.1 ± 0.01 -
epizonarene 1501 - - - 0.2 ± 0.04 - - 0.2 ± 0.05 - 0.2 ± 0.03 0.2 ± 0.04 -
β-bisabolene 1509 0.1 ± 0.00 0.3 ± 0.02 0.3 ± 0.06 0.3 ± 0.04 0.2 ± 0.01 - - - 0.9 ± 0.11 0.4 ± 0.09 -
(E,E)-α-farnesene 1509 - - - - - 0.3 ± 0.01 0.4 ± 0.08 0.4 ± 0.06 - - 0.4 ± 0.01
β-curcumene 1513 - 0.1 ± 0.01 0.2 ± 0.05 0.2 ± 0.03 - - - - - - -
trans-γ-cadinene 1513 0.5 ± 0.01 0.1 ± 0.00 0.3 ± 0.06 0.2 ± 0.01 - 0.1 ± 0.01 - - 0.4 ± 0.03 0.2 ± 0.03 -
sesquicineole 1516 - 0.6 ± 0.03 - - - - - - - - -
7-epi-α-selinene 1517 0.4 ± 0.37 - 0.4 ± 0.05 0.6 ± 0.08 0.3 ± 0.01 - - - - - -
(Z)-γ-bisabolene 1519 - - - - - - - - - - -
β-cadinene 1519 0.3 ± 0.01 0.2 ± 0.01 - 0.1 ± 0.14 - 0.2 ± 0.01 0.2 ± 0.02 0.2 ± 0.02 0.4 ± 0.05 0.3 ± 0.05 0.1 ± 0.05
trans-calamenene 1524 - - - - - 0.1 ± 0.05 - - - - -
δ-cadinene 1524 0.5 ± 0.03 0.4 ± 0.02 0.6 ± 0.06 0.5 ± 0.07 0.2 ± 0.02 0.2 ± 0.01 0.1 ± 0.01 0.2 ± 0.02 0.5 ± 0.10 0.3 ± 0.07 0.1 ± 0.01
selina-3,7(11)-diene3 1530 5.2 ± 0.47BC;a 3.2 ± 0.05DE;a 2.1 ± 0.65DEF;a 3.8 ± 0.55CD;a 1.3 ± 0,13F;a 3.8 ± 0.26CD;a 3.4 ± 0.33DE 3.1 ± 0.20DE;a 8.6 ± 1.01A;a 5.6 ± 1.3B;a 1.9 ± 0.09EF;a
(E)-γ-bisabolene 1531 - - - - - - - - - - -
α-calacorene 1543 0.4 ± 0.05 - 0.2 ± 0.01 0.3 ± 0.03 - 0.4 ± 0.04 0.2 ± 0.01 0.2 ± 0.02 - - 0.1 ± 0.01
cis-sesquisabinene hydrate 1545 - - 0.2 ± 0.05 - 0.1 ± 0.11 - - - - - -
elemol 1550 0.4 ± 0.04 0.4 ± 0.04 0.4± 0.09 0.4 ± 0.06 0.6 ± 0.09 0.2 ± 0.05 0.2 ± 0.04 0.2 ± 0.02 0.2 ± 0.00 0.3 ± 0.04 0.2 ± 0.02
guaia-3,9-diene 1556 - - 0.1 ± 0.10 - - - - - - - -
(E)-nerolidol 1564 0.6 ± 0.04 1.2 ± 0.04 0.9 ± 0.36 0.8 ± 0.07 0.7 ± 0.12 1.2 ± 0.13 0.3 ± 0.04 0.6 ± 0.12 0.9 ± 0.11 1.5 ± 0.27 0.6 ± 0.01
palustrol 1568 - - 0.4 ± 0.15 - - - - - - - -
caryophyllene alcohol 1570 - - - - - - - - - - -
spathulenol 1577 - - - - - - - - - - -
trans-sesquisabinene hydrate 1581 - 0.1 ± 0.05 0.2 ± 0.05 0.1 ± 0.06 - - - - - - -
caryophyllene oxide3 1582 11.8 ± 1.18BCD;b 11.3 ± 0.85BCD;b 10.9 ± 3.38BCDE;a 13.9 ± 0.24BC;a 22.7 ± 0.45A;a 14.4 ± 1.22B;a 7.0 ± 1.06E;b 9.9 ± 0.78CDE;a 9.1 ± 0.74DE;a 12 ± 2.03BCD;a 9.2 ± 0.11DE;b
globulol 1583 - - - - - - - - - - -
trans-(Z)-α-bisabolene epoxide 1586 - - 0.5 ± 0.16 - - - - - - - -
isoaromadendrene epoxide 1589 0.5 ± 0.10 0.5 ± 0.02 - 0.5 ± 0.06 0.8 ± 0.01 0.7 ± 0.07 0.3 ± 0.01 0.5 ± 0.04 0.5 ± 0.07 0.5 ± 0.08 0.4 ± 0.01
epi-globulol 1590 - - - - 0.1 ± 0.01 - - - - - -
viridiflorol 1592 0.2 ± 0.03 0.3 ± 0.05 - 0.3 ± 0.04 0.8 ± 0.04 0.2 ± 0.04 0.1 ± 0.02 0.2 ± 0.00 0.3 ± 0.07 0.2 ± 0.04 -
guaiol 1596 - - 0.3 ± 0.09 - - - - - - - -
humulene oxide I3 1608 4.2 ± 0.58BCD;b 4.1 ± 0.55BCD;b 4.8 ± 1.08BC;a 4.9 ± 0.19BC;a 9.3 ± 0.46A;a 5.2 ± 1.40B;a 2.4 ± 0.24D;a 3.6 ± 0.32BCD;a 3.4 ± 0.28BCD;a 4.0 ± 0.58BCD;a 3.1 ± 0.03CD;b
cedrenol 1610 0.6 ± 0.11 0.1 ± 0.07 - 0.4 ± 0.03 - 0.5 ± 0.25 0.2 ± 0.00 0.3 ± 0.02 0.3 ± 0.02 0.2 ± 0.02 -
humulane-1-6-dien-3-ol 1613 - - 0.3 ± 0.03 - - - - - - - -
selin-6-en-4-ol3 1618 1.1 ± 0.02CDE;a 1.1 ± 0.23CDE;a 0.5 ± 0.17E;b 1.2 ± 0.08CD;a 0.6 ± 0.05DE;b 2.0 ± 0.55A;a 0.8 ± 0.23CDE;b 0.8 ± 0.11CDE;b 1.9 ± 0.06AB;a 1.3 ± 0.14BC;a 0.7 ± 0.11DE;b
13-nor-valenc-1(10)-en-11-one 1629 - 0.2 ± 0.01 0.4 ± 0.06 0.5 ± 0.05 - - - - 1.0 ± 0.04 0.3 ± 0.34 0.2 ± 0.01
1-epi-cubenol 1627 0.4 ± 0.10 0.3 ± 0.07 0.4 ± 0.06 0.3 ± 0.26 0.5 ± 0.06 0.5 ± 0.10 0.2 ± 0.04 0.2 ± 0.07 0.2 ± 0.00 0.4 ± 0.04 0.2 ± 0.01
γ-eudesmol 1631 - - - - - - - - - - -
caryophylla-4(14),8(15)-dien-5-ol (unidentified isomer 1)3 1633 0.7 ± 0.69F;b 2.7 ± 0.46AB;b 2.5 ± 0.25ABC;b 2.6 ± 0.19AB;a 2.7 ± 0.27AB;b 3.0 ± 0.60A;a 1.4 ± 0.15DEF;a 0.9 ± 0.10EF;b 1.6 ± 0.06CDEF;b 2.3 ± 0.13ABCD;b 1.7 ± 0.09BCDE;b
caryophylla-4(14),8(15)-dien-5-ol (unidentified isomer 2)3 1633 2.1 ± 0.21ABC;b 2.6 ± 0.54AB;b 2.8 ± 0.30A;a 2.6 ± 0.16AB;b 2.7 ± 0.31A;b 1.8 ± 0.44BCD;a 1.2 ± 0.09D;b 1.3 ± 0.04D;b 1.2 ± 0.03D;b 2.2 ± 0.12ABC;b 1.6 ± 0.07CD;b
T-cadinol 1641 - - 0.3 ± 0.05 - - - - - - - -
cubenol 1641 - - - - - - - - 0.4 ± 0.02 - -
β-eudesmol 1649 0.2 ± 0.08 0.1 ± 0.00 - 0.2 ± 0.08 - 0.3 ± 0.09 - - - 0.2 ± 0.00 -
α-eudesmol 1653 - - - - - - - - - - -
neointermedeol 1655 - - 0.3 ± 0.06 0.1 ± 0.11 0.3 ± 0.02 1.2 ± 0.00 - - 0.2 ± 0.03 - 0.2 ± 0.00
bulnesol 1668 - - - - - - - - - - -
14-hydroxy-9-epi-(E)-caryophyllene3 1670 3.8 ± 0.50C;b 2.9 ± 0.56C;b 5.8 ± 0.62AB;a 5.4 ± 0.39B;b 7.0 ± 0.53A;b 5.5 ± 0.19B;b 2.5 ± 0.12C;b 3.0 ± 0.28C;b 3.6 ± 0.81C;b 3.6 ± 0.40C;b 2.7 ± 0.21C;b
ylangenal 1675 - 1.8 ± 1.66 - - 0.2 ± 0.02 0.2 ± 0.05 - - - 0.1 ± 0.06 -
aromadendrene epoxide II 1680 0.2 ± 0.03 0.2 ± 0.03 0.2 ± 0.05 0.2 ± 0.02 0.1 ± 0.01 0.1 ± 0.12 - 0.2 ± 0.01 0.1 ± 0.09 0.1 ± 0.06 0.1 ± 0.02
α-bisabolol3 1685 0.4 ± 0.06E;a 1.7 ± 0.36BC;b 0.8 ± 0.12DE;a 0.4 ± 0.04E;b 0.3 ± 0.03E;a 1.2 ± 0.06CD;a 1.1 ± 0.13CD;a 0.6 ± 0.07DE;b 5.2 ± 0.49A;a 2.2 ± 0.36B;b 1.1 ± 0.04CD;a
cedr-8-en-13-ol 1688 - - - - - - - - - - -
juniper camphor 1694 1.0 ± 0.06 1.0 ± 0.24 0.4 ± 0.07 0.8 ± 0.08 0.5 ± 0.02 1.8 ± 0.03 0.9 ± 0.06 0.7 ± 0.07 1.0 ± 0.05 0.9 ± 0.18 0.7 ± 0.02
(Z)-α-trans-bergamotol 1700 - - - - - 0.2 ± 0.02 - - - - -
α-phellandrene dimer 1801 - - 0.1 ± 0.02 - - - - - - - -
nootkatone 1803 - - - - 0.2 ± 0.01 0.2 ± 0.01 - - - - -
(E,E)-farnesyl acetate 1843 - - 0.2 ± 0.02 - - - - - - - -
hexahydrofarnesylacetone3 1845 0.6 ± 0.11D;a 0.6 ± 0.15D;b 1.7 ± 0.24BC;a 1.0 ± 0.21D;a 1.9 ± 0.11B;a 2.3 ± 0.11A;a 0.8 ± 0.14D;b 1.5 ± 0.05C;b 0.7 ± 0.03D;b 0.7 ± 0.13D;a 0.7 ± 0.01D;b
1-hexadecanol 1877 - - - - - - - 0.1 ± 0.07 0.1 ± 0.05 - 0.1 ± 0.05
(E,E)-farnesyl acetone 1918 - - 0.6 ± 0.12 - 0.6 ± 0.03 0.2 ± 0.06 - - - 0.1 ± 0.01 -
m-camphorene 1952 0.1 ± 0.01 - 0.2 ± 0.06 0.1 ± 0.01 - 0.1 ± 0.02 0.3 ± 0.08 0.3 ± 0.03 0.1 ± 0.01 - 0.3 ± 0.00
p-camphorene 1986 0.2 ± 0.10 0.1 ± 0.06 0.5 ± 0.07 0.4 ± 0.07 - - 0.6 ± 0.11 0.6 ± 0.09 - - 0.6 ± 0.00
ethyl hexadecanoate 2000 - - 0.1 ± 0.07 - - - - - - - -
phytol3 2112 0.5 ± 0.14CD;b 0.4 ± 0.18D;b 0.8 ± 0.27BCD;b 0.4 ± 0.05D;b 3.2 ± 0.11A;a 2.7 ± 0.04A;b 0.9 ± 0.06BC;a 0.7 ± 0.19BCD;b 1.0 ± 0.07B;b 0.8 ± 0.23BCD;a 0.9 ± 0.11BC;a
cannabidiol3 2369 23.2 ± 6.13BCDE;a 21.8 ± 0.66BCDE;a 28.2 ± 1.37ABCD;b 20.9 ± 3.94CDE;a 16.4 ± 0.36DE;a 14.5 ± 1.27E;b 35.9 ± 4.68A;b 29.6 ± 2.31ABC;a 22.2 ± 2.61BCDE;a 21.3 ± 10.13CDE;a 33.8 ± 0.98AB;a
cannabichromene 2373 0.7 ± 0.36 0.7 ± 0.23 0.4 ± 0.23 0.7 ± 0.25 0.7 ± 0.11 0.4 ± 0.14 1.2 ± 0.39 1.1 ± 0.11 0.7 ± 0.12 0.5 ± 0.29 1.1 ± 0.07
Δ9-tetrahydrocannabinol 2468 0.3 ± 0.09 0.4 ± 0.06 0.5 ± 0.01 0.2 ± 0.03 0.2 ± 0.00 0.2 ± 0.04 0.6 ± 0.16 0.5 ± 0.04 0.3 ± 0.08 0.3 ± 0.22 0.6 ± 0.01
Total identified (%) 94.5 ± 0.66 97.7 ± 0.08 98.1 ± 0.63 97.4 ± 0.09 99.4 ± 0.08 92.9 ± 1.03 96.9 ± 0.34 97.2 ± 0.25 95.8 ± 0.86 96.1 ± 1.06 97.2 ± 0.23
Monoterpene hydrocarbons 4.3 ± 0.71BCD;a 4.1 ± 1.57BCD;a 1.8 ± 0.52DE;a 2.0 ± 0.36DE;a 4.0 ± 0.60BCD;a 1.2 ± 0.15E;a 7.5 ± 0.42A;a 5.7 ± 2.07AB;a 3.7 ± 0.01BCDE;a 2.5 ± 0.85CDE;a 4.7 ± 0.35BC;a
Oxygenated monoterpenes 0.5 ± 0.10DE;a 0.9 ± 0.34D;b 0.3 ± 0.06E;a 0.2 ± 0.05E;a 0.5 ± 0.07DE;a 0.9 ± 0.15D;a 1.8 ± 0.20BC;a 2.3 ± 0.30A;a 1.4 ± 0.12C;a 0.6 ± 0.06DE;a 2.0 ± 0.10AB;a
Sesquiterpene hydrocarbons 35.5 ± 2.88A;a 35.6 ± 2.00A;a 29.6 ± 6.37AB;a 35.8 ± 3.03A;a 21.3 ± 0.88B,a 29.7 ± 3.84AB;a 28.5 ± 1.67AB;a 31.8 ± 3.45AB;a 34.5 ± 2.15A;a 36.9 ± 8.42A;a 29.6 ± 1.31AB;a
Oxygenated sesquiterpenes 28.2 ± 2.24CD;b 33.1 ± 4.36BC;b 33.2 ± 7.07BC;a 35.6 ± 1.25BC;a 50.3 ± 0.95A;b 40.3 ± 4.64B;a 18.6 ± 2.13E;b 22.9 ± 1.59DE;b 30.9 ± 0.22CD;b 32.3 ± 2.09BC;b 22.9 ± 0.47DE;b
Diterpene hydrocarbons 0.4 ± 0.11BC;a 0.1 ± 0.06D;a 0.9 ± 0.14A;a 0.5 ± 0.08B;a -D 0.1 ± 0.02CD;a 1.0 ± 0.19A;a 0.8 ± 0.12A;a 0.1 ± 0.01CD;a -D 0.9 ± 0.00A;a
Oxygenated diterpenes 0.5 ± 0.14CD;b 0.4 ± 0.18D;b 0.8 ± 0.27BCD;b 0.4 ± 0.05D;b 3.2 ± 0.11A;a 2.7 ± 0.04A;b 0.9 ± 0.06BC;a 0.7 ± 0.19BCD;b 1.0 ± 0.07B;b 0.8 ± 0.23BCD;a 0.9 ± 0.11BC;a
Phenylpropanoids 0.2 ± 0.06AB;a 0.1 ± 0.07CD;a -D 0.1 ± 0.03BC;a 0.3 ± 0.01A;a -D -D -D -D 0.2 ± 0.07AB;a -D
Cannabinoids 24.2 ± 6.57BCDE;a 22.8 ± 0.94BCDE;a 29.1 ± 1.61ABCD;b 21.8 ± 4.21CDE;a 17.4 ± 0.47DE;a 15.0 ± 1.45E;b 37.7 ± 5.23A;a 31.3 ± 2.45ABC;a 23.3 ± 2.80BCDE;a 22.1 ± 10.63CDE;a 35.5 ± 0.91AB;a
Apocarotenoids 0.6 ± 0.11C;b 0.6 ± 0.15C;b 2.4 ± 0.38A;a 1.0 ± 0.21C;b 2.5 ± 0.13A;a 2.5 ± 0.06A;b 0.8 ± 0.14C;b 1.5 ± 0.05B;b 0.7 ± 0.03C;b 0.8 ± 0.14C;a 0.7 ± 0.01C;b
Other non-terpene derivatives 0.1 ± 0.07B;a -B 0.1 ± 0.07B;a -B 0.1 ± 0.08B;a 0.4 ± 0.10A;a 0.1 ± 0.10B;a 0.2 ± 0.11B;a 0.1 ± 0.12B;a -B 0.1 ± 0.12B;a
Extraction yield (% w/w) 0.12 ± 0.01CD;a 0.23 ± 0.02A;a 0.12 ± 0.00CD;a 0.17 ± 0.01ABC;a 0.03 ± 0.00E 0.05 ± 0.01DE;a 0.13 ± 0.00DE;a 0.20 ± 0.02AB;a 0.20 ± 0.00AB 0.14 ± 0.04BC;a 0.16 ± 0.01ABC;a