Richard E. Carlson

Dr. Richard E. Carlson

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 April 2021 in Molecules
Verified
Journal Article
Open access
PDF file
TWTyler Wilson
Tyler Wilson
APAriel Poulson
Ariel Poulson
CCChris Chris
Chris Chris
RCRichard E. Carlson
Richard E. Carlson
RBR. Michael Buch
R. Michael Buch
Lavandula angustifolia Mill. (lavender) is an essential-oil-bearing plant in the Lamiaceae family. Volatile oil produced through the steam distillation of lavender was examined to establish the essential oil yield and aromatic profile from each portion of the plant—namely, the corolla, calyx, leaf, and whole flowering top. The resulting essential oils were analyzed by GC-FID and GC-MS. The different plant parts generally shared similar compounds but in varying relative percentages. Aromatic profiles of the whole flowering top and calyx were similar, with prominent compounds being linalool acetate (34.3%, 32.0%), linalool (26.5%, 32.9%), lavandulyl acetate (5.6%, 4.9%), terpinen-4-ol (5.3%, 7.0%), and (Z)-β-ocimene (4.5%, 5.4%), respectively. Aromatic profiles for the corolla and leaf were unique. Prominent aromatic compounds of the corolla included linalool acetate (18.4%), linalool (10.8%), epi-α-cadinol (10.0%), borneol (7.3%), and lavandulyl acetate (6.3%). Prominent aromatic compounds of the leaf included epi-α-cadinol (19.8%), γ-cadinene (11.0%), borneol (6.0%), caryophyllene oxide (4.9%), and bornyl acetate (4.8%). Complete profiles and essential oil yields of corolla, calyx, leaf, and whole flowering top were established. This study establishes the influence the corolla, calyx, and leaf exert on the aromatic profile of the whole flowering top and provides insight into authentication of lavender essential oil.

12 January 2024 in Plants
Verified
Journal Article
Open access
PDF file
BMBrett J. Murphy
Brett J. Murphy
TWTyler Wilson
Tyler Wilson
EZEmma A. Ziebarth
Emma A. Ziebarth
Christopher Ryan BowerbankChristopher Ryan Bowerbank
Christopher Ryan Bowerbank
RCRichard E. Carlson
Richard E. Carlson
The aromatic compound (E)-anethol is widely used in the flavor, fragrance, and medicinal industries. This compound is commonly produced through steam distillation of fennel, star anise, and anise seed. Given the cost of production, these natural and authentic essential oils are commonly adulterated with lower-cost natural materials or synthetic alternatives. The current study investigates essential oil profiles (gas chromatography/mass spectrometry) and stable isotope ratios (gas chromatography/isotope ratio mass spectrometry) of the abundant compound (E)-anethol in both authentic reference standards (n = 15) and commercially available samples (n = 30). This multifaceted analytical approach establishes techniques for ensuring the authenticity of essential oil sources of (E)-anethol and was then used to evaluate the current essential oil market sources of (E)-anethol. These findings report that adulteration of (E)-anethol-containing natural products takes various forms, and a multifaceted analytical approach is recommended for authentication. Of the commercial samples analyzed for this report, 27% were adulterated.

24 May 2021 in Journal of Essential Oil Research
Verified
Journal Article
Open access
BMBrett J. Murphy
Brett J. Murphy
RCRichard E. Carlson
Richard E. Carlson
JHJohn D. Howa
John D. Howa
TWTyler Wilson
Tyler Wilson
RBR. Michael Buch
R. Michael Buch
The essential oils of wintergreen and birch are composed primarily of methyl salicylate. Because this compound can easily be synthesized, wintergreen and birch oils are frequently adulterated. By using Gas chromatography-combustion/pyrolysis-isotope ratio mass spectrometry (GC-C/P-IRMS) in conjunction with TC/EA-IRMS, GC-FID, GC-MS, and 14C radiocarbon dating, criteria will be established that can be used to distinguish authentic and natural wintergreen and birch essential oils from adulterated ones or from synthetic methyl salicylate. Commercially purchased samples were compared to both synthetic ‘oil of wintergreen’ (methyl salicylate) and to natural birch and wintergreen essential oils obtained from trusted sources or from the steam distillation of fresh plant material. δ2HVSMOW, δ13CVPDB, and δ18OVSMOW IRMS results provide a clear distinction between authentic and adulterated essential oil samples.

2 November 2023 in Journal of Essential Oil Research
Verified
Journal Article
Open access
TWTyler Wilson
Tyler Wilson
APAriel Poulson
Ariel Poulson
BMBrett J. Murphy
Brett J. Murphy
BNBrandon Nebeker
Brandon Nebeker
ACAurélien Cuchet
Aurélien Cuchet
RCRichard E. Carlson
Richard E. Carlson

27 April 2022 in Molecules
Verified
Journal Article
Open access
PDF file
TWTyler Wilson
Tyler Wilson
BMBrett J. Murphy
Brett J. Murphy
AMAdrian Abad Mihalache
Adrian Abad Mihalache
CCChris Chris
Chris Chris
APAriel Poulson
Ariel Poulson
RCRichard E. Carlson
Richard E. Carlson
Ocimum campechianum Mill. (Peruvian basil) is an essential oil-bearing plant of the Lamiaceae family. Volatile oil produced through steam distillation of Peruvian basil was examined to establish the aromatic and stable isotope profiles of samples (n = 9) from three different cultivated plots in Peru. The resulting essential oils were analyzed by GC/FID, GC/MS, and GC/IRMS. In accordance with findings from other researchers, multiple chemotypes, defined by the most abundant aromatic compounds, exist within these populations. Overall, 55% of samples are the eugenol chemotype (values ranging 15.4–30.2%), 33% are the methyl eugenol chemotype (values ranging 68.1–68.7%), and a single sample is a mixture of both chemotypes, containing high levels of both eugenol (38.1%) and methyl eugenol (8.6%). Stable isotope ratios, δ2H and δ13C, performed on prominent compounds provide supporting data for distinguishing chemotypes. Complete aromatic profiles, stable isotope ratios, and essential oil yield are established for each sample. This study confirms the existence of multiple chemotypes and, for the first time, to the author’s best knowledge, establishes stable isotope ratios for O. campechianum essential oil, which proves a useful tool in further investigating plant metabolism and determining essential oil authenticity.

15 July 2025 in Agrochemicals
Verified
Journal Article
Open access
PDF file
TWTyler Wilson
Tyler Wilson
ALAlma Laney
Alma Laney
ZRZabrina Ruggles
Zabrina Ruggles
RCRichard E. Carlson
Richard E. Carlson
The conventional agricultural industry largely relies on pesticides to maintain healthy and viable crops. Application of fungicides, both pre- and post-harvest of crops, is the go-to method for avoiding and eliminating Botrytis cinerea, the fungal pathogen responsible for gray mold. However, conventional fungicides and their residues have purported negative environmental and health impacts. Natural products, such as essential oils, are viewed as a promising alternative to conventional fungicides. The current research is an in vitro study on the antifungal activity of a natural water-based fungicide (N.F.), which uses a blend of essential oils (ajowan, cassia, clove, eucalyptus, lemongrass, oregano) as the active ingredients against B. cinerea. Compared to conventional fungicides tested at the same concentration (50 μL/mL), those with active ingredients of myclobutanil or propiconazole; the N.F. demonstrated significant (F(3,16) = 54, p = <0.001) and complete fungal growth inhibition. While previous research has largely focused on the antifungal properties of single essential oils and/or isolated compounds from essential oils, this research focuses on the efficacy of using a blend of essential oils in a proprietary delivery system. This research is of importance to the fields of agronomy, ecology, and health sciences.