School of Water, Energy and Environment (SWEE)

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Browsing School of Water, Energy and Environment (SWEE) by Supervisor "Alamar, M. Carmen"

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    ItemOpen Access
    Biochemical and biomedical studies on African walnut (Tetracarpidium conophorum -Mull. Arg.) – a postharvest perspective
    (Cranfield University, 2015-10) Nkwonta, Chikere Godwin; Terry, Leon A.; Cellek, Selim; Alamar, M. Carmen
    African Walnut (Tetracarpidium conophorum- Mull. Arg) is a perennial climbing shrub which grows mainly in the Western region of Africa. It is found mainly in Nigeria, Gambia, Sierra Leone, Gabon, Equatorial Guinea and Cameroon as well. The nuts are encased in pods which may contain between 2 to 5 nuts. The seed is enclosed in a hard shell-like case. The nuts are commonly processed by boiling or roasting and consumed as a snack or used as soup thickener. In ethnobotanical medicine, the nut extract is extensively used in decoctions for treatment and/or management of common and chronic ailments such as malaria, dysentery, high blood pressure, diabetes and cancer. The nuts are generally exposed to high temperatures (25 – 37 °C) and relative humidity (RH) which increases susceptibility to fungal contamination and nutrient degradation, hence, raising concerns over product quality and safety. Experiment simulating the common retail postharvest storage and processing practices was conducted to: (i) determine the effects on the fatty acid profile; (ii) assess the impact on the fungal population contaminating the nut shells at different maturity stages, and potential mycotoxigenic implications; (iii) evaluate the cytotoxicity of four extract of the nut on lung cancer (A549) cells; and finally (iv) assay the total phenolic content and profile potential individual phenolic components of the nut. Results indicated the presence of essential and non-essential fatty acids namely; palmitate, oleate, stearate, linoleate, arachidate and α-linolineate with α-linolineate being the most abundant (1.1 – 8.2 mg/g freeze-dry weight). Boiling and roasting generally improved the concentration of the fatty acids best when nuts are cold stored at 5 °C for maximum of 10 days. Potential mycotoxigenic species - Aspergillus section Nigri, Aspergillus flavus/Parasiticus, Fusarium spp. and Penicillium spp. - were frequently isolated from cultured shell pieces of stored nuts. When compared with unprocessed nuts, roasting completely prevented fungal contamination in shell pieces from nuts in the non-stored (NSN) group at early maturity stage, while boiling significantly reduced the level of contamination to about 58 % (P < 0.05). Simulating open market conditions caused 100% fungal contamination in all boiled samples and roasted samples at early maturity. Mycotoxin analysis using Yeast Extract agar (YES) and High Performance Liquid Chromatography (HPLC) - Fluorescence detector (FLD) showed that Aflatoxins - G1 (AFG1), B1 (AFB1), G2 (AFG2), and B2 (AFB2) were produced by 20 isolates with both AFG1 and AFB1 being predominant at concentration ranges 4 – 32,200 and 4 – 22,700 ng/g plug weight, respectively. No Ochratoxin A (OTA) was detected. Phenolic component analysis indicated unprocessed (20.79 ± 1.0 mg gallic acid equivalent per gram freeze-dry weight – GAE/g FDW) samples showed the highest value for total phenolics while both boiling (9.90 ± 1.8 mg GAE/g FDW), and roasting (9.32 ± 2.7 mg GAE/g FDW) reduced the amount by more than 50 % when compared with unprocessed. Potential individual phenolic compounds were unambiguously separated using high performance liquid chromatography – diode array detector (HPLC-DAD). There were no differences between chromatograms of defatted and non-defatted unprocessed, roasted and boiled samples. Cytotoxicity evaluation showed no decrease in cell densities in plates treated with extracts from unprocessed nuts at all concentrations. Diethyl ether-ethyl acetate (10 µg/mL) and n-butanol (1000 and 500 µg/mL) extracts of roasted nuts as well as dichloromethane and water (1, 10 µg/mL) of boiled nuts caused a non-significant decrease of < 10 % in cell densities when compared with the phosphate buffered saline-media control. However, all extracts showed no cytotoxic effect on the A549 cells African walnut is basically produced at subsistence level in Nigeria, but considering the presence of desirable fatty acid profile and phenolic compounds, need for increased industrial scale production is herein recommended. Although fungal attack and potential mycotoxin risk on the nut may be high, retail processing by roasting has prospects to greatly accentuate the risk. Cold storage of the nut may help to improve the shelf life although it may not be cost effective for local farmers in Nigeria and Africa, however, it provides opportunity for export business. Although the nut extracts showed no cytotoxic effect on A549 lung cancer cell lines, there is need to investigate further to confirm it non-cytotoxicity activity on other cancer lines and normal cell lines.
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    ItemOpen Access
    Discovering biomarkers of postharvest resilience and flavour life in imported citrus and table grapes.
    (Cranfield University, 2022-02) Navarro-Calderon, Angela; Alamar, M. Carmen; Terry, Leon A.
    Clementines and table grapes, which are the main fruit crops consumed in the UK after bananas and apples, are considered non-climacteric fruit, not showing an increase in respiration rate and ethylene production during ripening. Previous research has suggested that a different ripening hormone, abscisic acid (ABA), has a more crucial role in the ripening of this kind of produce. The study presented herein aimed to identify biomarkers of postharvest resilience and flavour life of imported clementines and table grapes. For these studies two experiments were designed with the common objectives of determining: 1) the pre- or postharvest factors influencing the postharvest produce quality – both physiological and biochemical, and 2) the role of ABA and ABA catabolites on fruit senescence. The main findings from these studies were that the canopy position of clementines significantly affected fruit postharvest quality and hormonal content. Fruit located on the inside canopy showed higher RR and lower sugar content than outside fruit at the end of postharvest storage, resulting in a shorter shelf- life. At the same time, inside fruit showed a higher content of ABA and ABA catabolites than outside fruit, coinciding with a lower consumer preference score for external appearance, aroma and flavour. This is the first study that determined the ABA and ABA catabolite contents in the pulp of clementines from different canopy positions during senescence, and related this to consumer acceptance. The use of an ethylene inhibitor, 1-methylcyclopropane (1-MCP), during the postharvest storage of table grapes was investigated. The treatment did not have a positive effect on their postharvest quality; in fact, grapes were significantly affected by mould incidence at the end of the shelf-life. The hormonal content in different berry sections was also evaluated; the distal section, which showed a higher mould incidence than the proximal, had three times more ABA and ABA catabolites than the proximal section. This is the first time that the spatial distribution of ABA during the senescence of table grapes was profiled. Despite being different products, similar novel results were observed for both clementines and table grapes. This study indicated that senescence processes in these non-climacteric produce was initiated after a significant increase in RR, and that ABA could be considered a biomarker for clementines and table grapes senescence since an ABA peak during postharvest storage preceded an increase in RR, mould incidence, organic acids, and sucrose hydrolysis. This coincided with a decrease in berry firmness. These findings are of significant importance for the industry. Understanding how ABA regulates senescence processes and the quality changes taking place during postharvest cold storage of clementines and tables grapes improves the consistency in fruit quality and reduces waste and consumer complaints. Although clear beneficial findings have been identified, the results of this study were limited by time, resources, climatic conditions, and other factors. Therefore, recommendations for future work are: to perform molecular studies on genes regulating the ABA pathway from field to postharvest storage; to investigate the crosstalk between ABA, ethylene, and sucrose from ripening to senescence; and to further investigate the use of shade nets and harvesting by canopy position on fruit quality consistency and consumer acceptance.
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    ItemOpen Access
    Implementation of spectroscopy as a rapid measurement tool (RMT) to inform risk assessment at petroleum contaminated sites in the Niger Delta, Nigeria.
    (2018-04) Douglas, Kokah Douglas B.; Alamar, M. Carmen
    The recent developments and applications of rapid measurement tools (RMT) such as visible near-infrared (vis-NR) spectroscopy can provide ‘fit for purpose’ and cost effective data for informing risk assessment and managing oil-contaminated sites. Infrared spectroscopy discriminates between chemical compounds by detecting the specific vibrational frequencies of molecular bonds, producing a unique infrared ‘spectral signal’ thereby enhancing its identification and quantification applying chemometrics. The aim of the research was therefore to assess the potential of vis-NIR and mid-infrared (MIR) diffuse reflectance spectroscopy (DRS) techniques as RMT to inform risk decision support for remediation of petroleum contaminated sites. The objectives of the study were to: critically review chromatographic and spectroscopic methods for petroleum hydrocarbon analysis in soils; evaluate vis-NIR sensitivity to detect hydrocarbon concentration differences throughout weathering; predict TPH, PAH and alkanes concentrations in contaminated soils using vis-NIR and MIR DRS coupled with regression techniques. The study further evaluated which spectroscopy technique (vis-NIR or MIR); and which modelling method (RF or PLSR) performs best. In this study, a series of 13 soil mesocosms was set up where each soil sample collected was spiked with 10 ml of Alaskan crude oil and allowed to equilibrate at room temperature for 48 h before analysis. The mesocosms were incubated for two years at roomntemperature in the dark. Soils scanning and gas chromatography coupled to mass spectrometry (GC-MS) analysis were carried out at T0, 4, 12, 16, 20 and 24 months. Prior to scanning, soil samples were air-dried at room temperature (21oC) to reduce the effect of moisture. The soil scanning was done simultaneously using an AgroSpec spectrometer with a spectral range of 305 to 2200 nm (tec5 Technology for Spectroscopy, Germany) and Analytical Spectral Devices LabSpec2500 spectrometer (ASD Inc, USA) with a spectral range of 305 to 2500 nm to assess and compare the sensitivity and response of the two instruments to weathering and hydrocarbon composition change overtime against GC-MS data. Partial least squares (PLS) and random forest (RF) regression models showed that ASD LabSpec2500 performed better than tec5 which may be attributed to the shorter wavelength spectra range of the tec5 spectrometer and therefore not detecting all significant hydrocarbon signals (e.g., 2207, 2220, 2240 and 2460 nm). The sensitivity of the two spectral devices to weathering and REWARD K. DOUGLAS Cranfield University PhD Thesis, 2018 hydrocarbon composition change was, however, comparable; and the predicted concentrations were also comparable to the hydrocarbons concentrations determined by GC-MS. The results (coefficient of determination, R²=0.9; ratio of prediction deviation, RPD=3.79 and root mean square error of prediction, RMSEP=108.56 mg/kg) demonstrate that visible-near infrared diffuse reflectance spectroscopy (vis-NIR DRS) is a proven tool for rapid site investigation and monitoring without the need of collecting soil samples and lengthy hydrocarbon extraction for further analysis..To this end, 85 soil samples collected from three crude oil spill sites in the Niger Delta, Nigeria. Prior to spectral measurement, soil physiochemical properties such as pH, total organic carbon and textural analysis were carried out. Soil samples were scanned (field-moist) and assessed using ASD LabSpec2500 (wavelength 350-2500 nm) and MIR data was acquired with Agilent 4300 handheld Fourier transform infrared (FTIR) spectrometer (Agilent Technologies, Santa Clara, CA, United States) with a spectral range of 4000- 650 cmˉ¹. Specifically, detailed analysis of the hydrocarbon content including total petroleum hydrocarbons (TPH), aliphatic and aromatic hydrocarbon fractions were determined and quantified by GC-MS, vis-NIR and MIR DRS. MIR over-performed vis-NIR with RF modelling method performing better than PLSR in predicting TPH, PAH and alkanes. However, PLSR-vis-NIR produced slightly better results than PLSR- MIR in predicting TPH and alkanes. Overall, vis-NIR (wavelength 350-2500 nm) laboratory-scale study yields better TPH prediction than the field-scale study. The minimised moisture content may have improved the results, as laboratory-scale samples were air-dried. Based on the results, MIR spectroscopy coupled with RF is recommended for the analysis of hydrocarbon contaminated soil. Finally, spectroscopy approach was proposed as RMT for contaminated soil investigation and risk prioritisation.