| Literature DB >> 35964094 |
Navnath S Indore1, Chithra Karunakaran1,2, Digvir S Jayas3.
Abstract
Synchrotron imaging is widely used for research in many scientific disciplines. This article introduces the characteristics of synchrotron X-ray imaging and its applications in agriculture and food science research. The agriculture and food sector are a vast area that comprises of plants, seeds, animals, food and their products; soils with thriving microbial communities; and natural resources such as water, fertilizers, and organic matter. These entities have unique internal features, structures and compositions which differentiate them from each other in varieties, species, grades, and types. The use of a bright and tuneable monochromatic source of synchrotron imaging techniques enables researchers to study the internal features and compositions of plants, seeds, soil and food in a quick and non-destructive way to enhance their use, conservation and productivity. Synchrotron's different X-ray imaging techniques offer a wide domain of applications, which make them perfect to enhance the understanding of structures of raw and processed food products to promote food safety and security. Therefore, this paper summarizes the results of major experiments carried out with seeds, plants, soil, food and relevant areas of agricultural sciences with more emphasis on two synchrotron X-ray imaging techniques: absorption and phase-contrast imaging and computed tomography.Entities:
Keywords: Food imaging; Microcomputed tomography; Plant imaging; Seed imaging; Soil-root medium imaging; Synchrotron X-ray; X-ray absorption; X-ray phase-contrast
Year: 2022 PMID: 35964094 PMCID: PMC9375343 DOI: 10.1186/s13007-022-00932-9
Source DB: PubMed Journal: Plant Methods ISSN: 1746-4811 Impact factor: 5.827
Fig. 1Major components of a synchrotron X-ray imaging beamline system
(Source: Canadian Light Source, Saskatoon; www.lightsource.ca)
Fig. 2A Basic layout of synchrotron X-ray micro-CT [34] and B Setup of phase contrast micro-CT where sample to detector distance is adjustable [36, 66]
Fig. 3Schematic diagram of how X-rays pass through object. Dashed line shows X-ray wave without object, and solid with object. Upper curves: cross section corresponding to X-ray phase shift. Lower curves: cross section corresponding to X-ray absorption [72]
Fig. 4Phase retrieval, slice creation, and 3D reconstruction of a soil sample [36]
Synchrotron imaging operation parameters used in agriculture and food science research
| Technique | Material | Purpose/findings | Beamline and beam size (H, mm × V, mm) | Energy (keV) | Resolution (μm) | No of Projection or Increment angle (°) | Exposure per image/total time (s/min) | Field of view mm × mm | Detector/detector pixel | Voxel (mm/μm) | Source to detector(Sr/d) and sample to detector distance (Sl/d), cm | References |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Plants and fruits | ||||||||||||
| SR-XTM | Modern and Fossil plants | Internal structure | TOMCAT, Swiss (50 × 4) | 9.9 | 0.35 | 1500 | 0.42/10.5 | 1 × 1.4 | 2560 × 2160 | 400 × 400 × 400 μm | 100(Sl/d) | [ |
| SRPC-μCT | Canola plant | Water and nutrient transport | BMIT-Canadian light source (40 × 5) | 18, 24 | 4.3 | 1800, 5001 | 1/83 | 4 × 10 | 4000 × 2600 | 0.7 × 0.7 × 0.7 mm | 80, 60(Sl/d) | [ |
| SR-μCT | 18 | 8.75 | 1800 | 2.3/69 | 8.5(Sl/d) | |||||||
| SR-PCI | Wheat | Fusarium disease detection | 18 | 8.75 | *– | 1 s/– | 4000 × 2600 | 1 × 1 × 1 mm | 80(Sl/d) | [ | ||
| SRP-TM | Live vines of plant | Plant xylem network | ALS, Berkeley CA USA (40 × 4.6) | 10–18 | 4.5 | 720/0.25° | 0.1–1/40 | 8.3 × 18 | 4006 × 2672 | 5 × 5 × 5 μm | 1000 (Sr/d) | [ |
| SR-μCT | Rose peduncles | Effect of SR- X-ray and residence time on quality | BESSY II, Germany (200 × 100) μm | 30, 40, 50 | 4.56 | 1500/0.12° | 1.4, 1.2, 3/35 | 10 × 13 | 512 × 512 | 4.56 × 4.56 × 4.56 μm | 3500(Sr/d) | [ |
| SR-μCT | Wood | Microstructure changes under force and stress | DORIS III, DESY (20 × 3) | 9 | 2 | 720/0.25° | – | 1 × 1 | 1536 × 1024 | 1 mm3 | – | [ |
| SR-μCT | Wood | TOMCAT, SLS | 11 | 2.15 | 720/0.25° | 0.3/12 | 3.58 × 1.2 | 2048 × 2048 | 1.7 × 1.7 × 1.7 μm | 0.7 (Sr/d) | [ | |
| SR-μCT | Wood | Microstructural decay due to fungi | TOMCAT, Swiss | 15 | 20 | 2001 | 0.13/4.2 | 1650 × 1650 μm | 1560 × 2160 | 0.65 × 0.65 × 0.6 μm | 0.5 (Sl/d) | [ |
| SRP-μCT | Wheat | Host Interactions | BMIT-CLS, SK | 20 | 1800 | 0.8/24 | 1 × 1 | 13.12 μm3 | 20 (Sl/d) | [ | ||
| SR-μCT | Tomato leaves | 3D laminography | ID19 of ESRF, France (60 × 15) | 18 | 0.75 | 1200 | 0.5/10 | 1.54 × 1.54 | 2048 × 2048 | 750 × 750 × 750 nm | 35 (Sl/d) | [ |
| CO2 gas exchange in leaf | 20.5 | 0.75 | – | – | 150 × 150 | – | 1.4 × 1.4 × 1.4 μm | 3, 4.5, 10.5, 21.5 (Sl/d) | [ | |||
| SR-μCT | coast redwood samplings | Embolism In the xylem | ALS, Berkeley | 15 | 4.5 | 720/0.25° | 12 min | 5 × 5 | 4006 × 2672 | 175 × 175 × 500 μm | – | [ |
| SR-μCT | Ggrapevine | Xylem vessel refilling | 24 | 0.65 | 1025 | 60 min | 1.7 × 1.7 | – | 0.65 μm3 | – | [ | |
| SR-μCT | Sunflower | Drought-induced embolism in stems | SYRMEP Trieste (120 × 4) | 22 | 2.0 | 2048/1° | 250 ms/6 min | – | – | – | 10 (sl/d) | [ |
| SR-μCT | Ggrapevine | Visualizations of Drought-Induced Embolism | ALS, Berkeley (251 × 8) µm | 15 | 4.5 | 720/0.25° | 25 min | – | 4006 × 2672 | – | – | [ |
| SRP-μCT | Submerged leaves | visualise gas films on submerged leaves of common cordgrass | TOMCAT | 12 | 0.375 | 2001 | 10 min | 2048 × 2048 | 0.375 × 0.375 × 0.375 μm | 1.4–4.0(sl/d) | [ | |
| SR-PCI | Woody herbaceous plant leaves | With iodine contrast agent | APS,IL USA 207 × 15 μm | 7–20 | 1.66 | – | 0.4/- | 5 × 5 | 2048 × 2048 | – | 5500 (Sr/d) 1–10 (Sl/d) | [ |
| 10–60 | 3.56 | – | 1.7/- | 1392 × 1040 | – | 5500 (Sr/d) 1–20 (Sl/d) | ||||||
| Seeds | ||||||||||||
| SR-inline phase TM | Maize | Internal changes in feature | ID19, ESRF (60 × 15) μm | 17.6 | 5 | 1000 | 50 s/20 min | – | 2048 × 2048 | 5 × 5 × 5 μm | 100 (Sl/d) | [ |
| SR-XTM | Arabidopsis | Intercellular void network | 21 | 0.3 | 800/0.225° | 2 s/26 min | 0.6 × 0.6 | – | 5 × 5 × 5 μm | 14,500(Sr/d)and 1.3, 3.3, 6.3, 10.3(Sl/d) | [ | |
| HXRTM | Fossils & modern horse gram | Seed coat thinning with time | I132 of DLS UK (14.5 × 19) μm | 15 | – | 4000 | 0.15, 0.2, 0.25 s/16 min | – | 5120 × 5120 | 1 × 1 × 1 mm | 0.5 | [ |
| SRP-μCT | Rapeseeds | Distribution of storage oils | ESRF, Grenoble (200 × 200) µm | 19 | 0.75 | 1200 | 0.1 s/2 min | – | – | 0.74 μm3 | 9 (Sl/d) | [ |
| SR-XTM | Fossil seeds | Internal features of fossil flowers | TOMCAT, Swiss | 10, 12 | 0.37, 0.65, 0.74 | 570–660 | – | 0.85 × 30.7 | 10 × 20 μm | 0.65 × 0.65 × 0.65 μm | – | [ |
| SRP-μCT | Fossil flowers | Cretaceous fossil inflorescence | BM05 ESRF | 20 | 0.75 | 4000 | 1.2 s/80 min | FReLoN 8.8 μm | 2(Sl/d) | [ | ||
| SRP-nCT | Fossil flowers | Cretaceous fossil inflorescence | ID22-NI ESRF | 29.5 | 0.76 | 2000 | 0.8 s | FReLoN 20 μm | 4.7, 4.8, 5.2, 6.2 (Sl/d) | [ | ||
| Soil and roots | ||||||||||||
| SRP-μCT | Barley root hair in soil | Importance of root hairs on pore structure development at the root-soil interface | I13 DLS UK (1.7 × 1.7) | 15 to 21 | 1.6 | 1601 | 0.15 s/ 4 min | 4 9 × 3.5 | 2560 × 2560 | 2 × 2 × 1 mm | 6.35(Sl/d) | [ |
| SR-μCT | soil aggregation | Soil aggregation in an Ultisol | BL13W1, SSRF, Shanghai (50 × 5) | 28 | 9 | 430 | – | 2.70 × 3.2 | 1052 × 1052 | 9 × 9 × 9 μm | – | [ |
| SR-μCT | Ultisol under Wetting and drying | Intra-aggregate microstructure | 24 | 3.7 | 1300/0.10° | 1.8/39 | – | 1700 × 1700 | 541 × 541 × 541 | – | [ | |
| SR-μCT | Quantification of aggregate | Effect of vegetation on strcture | 24 | 3.25 | 550 | 30 s | 2048 × 2048 | 3.25 × 3.25 × 3.25 | 12 (sr/sl) | [ | ||
| SR-μCT | Two soil types of states USA | Characterization of soil microaggregates | ALS, Berkeley (251 µm × 8 µm) | 11 | 20 | 1800 | 1/30 | – | – | 325 nm | 0.8 (Sl/d) | [ |
| SR-μCT | Soil | Flow of sand | APS, 6.0 (50 × 5) | 33.70 | 17.1 | 720/0.25° two pass | 1.4/16 | 11.1 × 3.6 | 1317 × 1335 | 650 × 650 × 211 mm | – | [ |
| APS 1.5 (1.5 × 1) and (200 × 40) µm | 33.69 | 6.7 | 5/60 | 4.39 × 3.45 | 1300 × 1330 | 658 × 658 × 517 mm | – | |||||
| SR-μCT (KI contras) | Sand | Water content on compaction | BL13W1 SSRF | 20 | 0.65 | 1200 | –/150 | 13 × 13 | 2048 × 2048 | 0.65 × 0.65 × 0.65 μm | – | [ |
| SR-μCT at K-edge | Soil | Locate organic matter | HARWI II, Germany (50 × 10) | 30, 70, 78 | 9.77 | – | – | – | 4.89 μm | 3.8 × 3.5 × 3.30 mm | – | [ |
| SR-μCT | Two soil types | 3D pore network of grassland and tilled soil | DESY, Germany | Tilled: 21.5, grassland: 24 | 3.2, 5.4 | 0.5° | – | – | 1536 × 1024 | 400 × 400 × 400 | – | [ |
| SR-XTM | Soil-root | Growth of wheat root hairs | TOMCAT | 20 | 1.0 | 1501 | – | 500 × 500 × 500 | – | [ | ||
| Food | ||||||||||||
| HRXTM | Soft cereal foods | Impact of protein reinforcement on the deformation | BM05, ESRF, Grenoble | 19 | 11 × 11 | – | 2 s | 11 × 22 5 × 10 1 × 2 | 2016 × 2016 | 11 μm 5.5 μm 1.1 μm | – | [ |
| SR-XTM | Bread | Bubble growth and foam setting | 18 | – | 400 | 0.02/0.13 | 628 × 628 × 256 mm | [ | ||||
| SR-XTM | Pome Fruits (apple, pear) | Gas network architecture | ID15 EPSRF (3.2 × 3.2) | 25 | 2.5 | 900 | 1/0.5 | 2048 × 2048 | 1.9 μm3 | 3800(Sr/d) | [ | |
| SR-PCI | Characterization of fruit tissue | ID19, EPSRF | 18 | – | 700 | – | 0.7 × 0.5x 1 mm3 | - | 0.95 μm3 | 20.7 | [ | |
| SR-μCT, SRP-μCT | Gas exchange pathways | 18 | 1.4, 5.1 PCI: 0.7 | 1200 | 0.5/10 | 1.43 × 1.43 | 2048 × 2048 | 712 nm | 10,000 (Sr/d), 3.5 (Sl/d) | [ | ||
| SR-μCT | Extruded cereal & biscuit | Internal structure | 17.6 | 6.5, 7.5, 16.2, 25.8 | 2000–5000 | 0.2/15 | – | 2048 × 2048 | 7.5 μm (2048 × 2048 × 1024) | – | [ | |
| SR-μCT | Noodle dough | Characterization of bubbles | BMIT CLS | 25 | 8.75 | 600/0.30 | 0.04/1.10 | – | 4000 × 248 pixels | 10–97 voxel | 80 (Sl/d) | [ |
| SR-μCT | Ice cream | Temp dependence microstructure | (I13-2) DLS, U.K | 15 to 30 | 0.8 | 900 | 0.1/1.5 | – | 2560 × 2160 pixel | 2 k × 2 k × 2 k | 3.5 (Sl/d) | [ |
| SRP-μCT | 15 to 30 | 3601 | 0.1/6 | – | [ | |||||||
| SR-μCT | Wheat flour | Bubble size distribution in dough | BMIT-BM 05B1-1 CLS, SK 40 × 5 mm | 18 | 8.75 | 350/1.5° | 0.2/2 | – | 530 × 2530 | 7–25 voxels | 147 (Sl/d) 2620 (Sr/d) | [ |
| SR-μCT | Coffee Beans | Voids/pore volume distribution of green and roasted coffee beans | SYRMEP, Trieste (Italy) | 19, 20 | 4.5 | 1440/0.1250 | – | 18 × 12 | 4008 × 2672 | 1 mm3 | 20 (Sl/d) | [ |
| SR-μCT | Chocolate | Migration pathways through cracks and voids | (DESY) Hamburg | 13 | 1.0 | 1800 | 1/20 | 1.8 × 1.8 mm | 3056 × 3056 | 100 μm | – | [ |
| SRP-μCT | Fish | Histology | APS, ANL USA | 13.8, 16.2 | 1.43 | 2048 | 20/20 | – | – | 0.743 μm3 | 3 (Sl/d) | [ |
Sl/d sample to detector, Sr/d source to detector distance, μCT micro computed tomography, TM tomography
Fig. 5Left: X-ray images and Right: 3D segmentation of maize seeds at four different developmental stages corresponding to 7, 9, 12 and 21 days after pollination [26]
Fig. 63D model of void spaces (A, B) in the hypocotyl of a developing rape seed (Brassica napus) [86] Copyright (2006) National Academy of Sciences and Virtual slice (C, D) of Arabidopsis seeds, void network and reconstructed voids in phase contrast imaging [2]
Fig. 7The 3D images showing internal details of canola plant in SRPµCT (A, B) of plants and SR-µCT (C, D). Histogram of gray values for absorption and phase contrast are given in E [1]
Fig. 8Top: Transverse high resolution CT micrographs of grapevine stems showing the radial, sectored spread of embolisms during the simulated drought experiments. Vessel lumen colour denotes the time point (hours) at which gas was first observed inside the vessel. Bars = 1 mm. Bottom: volume renderings of grapevine vessels showing a pathway for embolism spread between sectors and (B–D) Vessels in the red sector embolized first and then spread through a vessel (yellow) that drifted tangentially from the red sector to the blue sector [23]
Fig. 9Phase contrast X-ray images of healthy (1) and infected rachis (2) of wheat cultivars at four days after inoculation with FHB [90]
Fig. 10Schematic sequential diagram of the pore–throat network construction [34]
Fig. 11Steps involved in image processing of soil aggregate from left; volume rendering, pore space analysis, opening analysis and geometrical accessibility [38]
Fig. 12A 3D volume mesh is generated, with root hairs, soil, root surface and water, B section of a seminal root including lateral roots and root hairs and C 3D rendered barley root and hairs showing the surrounding soil [24, 41]
Fig. 13Dynamic bubble growth at increasing time period in dough in reconstructed synchrotron 3D X-ray images slices [44]
Fig. 14The virtual cut of 3D synchrotron X-ray images, where porosity in non-roasted (left set) is lower than roasted coffee bean (right set) [47]
Fig. 15Synchrotron X-ray image slices of different layers showing voids and cracks in chocolate samples [48]