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38 results for “carrot”
Trap catches of carrot fly (Psila rosae) and cutworm (Agrotis ipsilon) from 142 fields in Denmark and Southern Sweden 1997-2019
<p>The pests were caught in various vegetable crops in Denmark and Southern Sweden: Yellow sticky traps for carrot flies and pheromone traps for cutworm adults.</p> <p>The data is provided as both a tab-separated text file and a binary R data file. The R files provides code to read and plot the data. The two plots produced are also provided as PNG files.</p> <p>The data were collected by SEGES Innovation, Denmark.</p>
Data for Linkage mapping of root shape traits associated with market class in two biparental carrot populations
<p> </p> <p>This repository contains essential data to support the findings presented in the forthcoming publication titled "Linkage Mapping of Root Shape Traits Associated with Market Class in Two Biparental Carrot Populations." It includes VCF files for two distinct carrot biparental populations, as well as R code for filtering, constructing linkage maps, and conducting QTL analysis. Furthermore, the repository hosts phenotypic data gathered from these two biparental populations during the years 2020 and 2021.</p> <p>Two carrot genetic maps, one for each population, have been made available alongside their respective phenotypic data.</p> <p>The provided R code contains absolute working directory paths that may not function as intended on your system. The primary purpose of sharing this code is to offer readers insight into the techniques employed in this study. You may need to adapt the directory paths to suit your specific setup. </p> <p>To assist readers in understanding the logical sequence of steps involved in our linkage mapping project, the R code scripts have been sequentially numbered from 0 to 10.</p> <p>For more info contact: vegaalfaro@wisc.edu.</p>
OPTIMA - spray distribution data - bed-grown carrots boom sprayer
<p>Spray distribution data of 13 nozzle configurations, consisting of different nozzle types (standard flat fan, air-inclusion, off-center), nozzle size (ISO 02, 04), spray angle (80°, 110°), and number of nozzles (3 or 4 nozzles per bed), at different nozzle heights and distance, spraying at 300 kPa. </p> <p>Read 'Info' tab for more information.</p> <p>Data presented in Zwertvaegher et al. (2022). Boom sprayer optimizations for bed-grown carrots at different growth stages based on spray distribution and droplet characteristics. Pest Management Science. https://onlinelibrary.wiley.com/doi/10.1002/ps.6792 </p>
OPTIMA - average droplet velocity per droplet size interval - carrot boom sprayer
<p>Spray droplet velocity (average ± SD; m/s) per droplet size interval for 9 nozzle types, measured at 300 kPa and 50 cm below the nozzle using a PDPA laser based measuring set-up.</p> <p>Read 'Info' tab for more information.</p> <p>Data presented in Zwertvaegher et al. (2022). Boom sprayer optimizations for bed-grown carrots at different growth stages based on spray distribution and droplet characteristics. Pest Management Science. https://onlinelibrary.wiley.com/doi/10.1002/ps.6792 </p>
OPTIMA - droplet characteristics incl. air support data - bed-grown carrots boom sprayer
<p>Spray droplet size and velocity characteristics data of 4 nozzle types at 4 air support settings, measured at 300 kPa and 50 cm below the nozzle using a PDPA laser based measuring set-up.</p> <p>Read 'Info' tab for more information.</p> <p>Data presented in Zwertvaegher et al. (2022). Boom sprayer optimizations for bed-grown carrots at different growth stages based on spray distribution and droplet characteristics. Pest Management Science. https://onlinelibrary.wiley.com/doi/10.1002/ps.6792 </p>
OPTIMA - droplet characteristics data - bed-grown carrots boom sprayer
<p>Spray droplet size and velocity characteristics data of 9 nozzle types, measured at 300 kPa and 50 cm below the nozzle using a PDPA laser based measuring set-up.</p> <p>Read 'Info' tab for more information.</p> <p>Data presented in Zwertvaegher et al. (2022). Boom sprayer optimizations for bed-grown carrots at different growth stages based on spray distribution and droplet characteristics. Pest Management Science. https://onlinelibrary.wiley.com/doi/10.1002/ps.6792 </p>
A higher-level nuclear phylogenomic study of the carrot family (Apiaceae)
<p>Premise</p> <p>The carrot family (Apiaceae) comprises 466 genera, which include many well-known crops (e.g., aniseed, caraway, carrots, celery, coriander, cumin, dill, fennel, parsley, and parsnips). Higher-level phylogenetic relationships among subfamilies, tribes, and other major clades of Apiaceae are not fully resolved. This study aims to address this important knowledge gap.</p> <p>Methods</p> <p>Target sequence capture with the universal Angiosperms353 probe set was used to examine phylogenetic relationships in 234 genera of Apiaceae, representing all four currently recognized subfamilies (Apioideae, Azorelloideae, Mackinlayoideae, and Saniculoideae). Recovered nuclear genes were analyzed using both multispecies coalescent and concatenation approaches.</p> <p>Results</p> <p>We recovered hundreds of nuclear genes even from old and poor-quality herbarium specimens. Of particular note, we placed with strong support three incertae sedis genera (<em>Platysace</em>, <em>Klotzchia</em>, and <em>Hermas</em>); all three occupy isolated positions, with <em>Platysace</em>resolved as sister to all remaining Apiaceae. We placed nine genera (<em>Apodicarpum</em>, <em>Bonannia</em>, <em>Grafia</em>, <em>Haplosciadium</em>, <em>Microsciadium</em>, <em>Physotrichia</em>, <em>Ptychotis</em>, <em>Tricholaser</em>, <em>Xatardia</em>) that have never previously been included in any molecular phylogenetic study.</p> <p>Conclusions</p> <p>We provide support for the maintenance of the four existing subfamilies of Apiaceae, while recognizing that <em>Hermas</em>, <em>Klotzschia</em>, and the <em>Platysace</em> clade may each need to be accommodated in additional subfamilies (pending improved sampling). The placement of the currently apioid genus <em>Phlyctidocarpa</em> can be accommodated by the expansion of subfamily Saniculoideae, although adequate morphological synapomorphies for this grouping are yet to be defined. This is the first phylogenetic study of the Apiaceae using high-throughput sequencing methods and represents an unprecedented evolutionary framework for the group.</p>
On the emergence mechanism of carrot sprites
<p>This dataset includes the input and output files for the paper: On the emergence mechanism of carrot sprites.</p> <p>Intput files:</p> <p># <strong>Plasma-chemistry, diffusion and mobility coefficients</strong></p> <p>sprite_chemistry_basic.txt</p> <p># <strong>Configuration files</strong></p> <p>sprite_3d_simp.cfg</p> <p>m_user.f90</p> <p>Output files:</p> <p>sprite_3d_*.silo</p>
Carrot amphora from Traismauer (v 1.0.0)
Scaled virtual reconstruction of a so-called *carrot amphora* (Augst 44/Camulodunum 189/Schöne-Mau 15 | type *Bb* & rim *3b1* after Vipard [1995]) found at the *vicus* (civil settlement') of today's Traismauer, which belongs to the former ancient Roman fort of *Augustianis* were auxiliary troops (cavalry) were stationed. The fort was located at the Roman Danube frontier (so-called *limes*) in northeastern Noricum, which is today's Lower Austria. This amphora belongs to a convolute of Roman finds derived from a context excavated in the 1970s. *** # 📍 [Augustianis/Traismauer (Lower Austria)](https://goo.gl/maps/tziQrTZLcvW19fWH6) # *The framents were photogrammetry-scanned & processed & referenced in Agisoft Metashape & assambled & reconstructed in Blender.* * photos: K. Klein * photogrammetry & modeling: D. Hagmann/A. Langendorf --- Vipard, P. (1995). Les amphores carottes (forme Schöne-Mau XV). In: Actes du Congrès de Rouen (51–77) Source: Objaverse 1.0 / Sketchfab
Carrot amphora (foot) from Traismauer (v 1.0.0)
Scaled 3d-model of a so-called *carrot amphora's foot* (Augst 44/Camulodunum 189/Schöne-Mau 15 | type *Bb* & rim *3b1* after Vipard [1995]) found at the *vicus* (civil settlement') of today's Traismauer, which belongs to the former ancient Roman fort of *Augustianis* were auxiliary troops (cavalry) were stationed. The fort was located at the Roman Danube frontier (so-called *limes*) in northeastern Noricum, which is today's Lower Austria. This amphora belongs to a convolute of Roman finds derived from a context excavated in the 1970s. *** # 📍 [Augustianis/Traismauer (Lower Austria)](https://goo.gl/maps/tziQrTZLcvW19fWH6) # *The frament was photogrammetry-scanned & processed & referenced in Agisoft Metashape & assambled & reconstructed in Blender.* * photos: K. Klein * photogrammetry & modeling: D. Hagmann/A. Langendorf --- Vipard, P. (1995). Les amphores carottes (forme Schöne-Mau XV). In: Actes du Congrès de Rouen (51–77) Source: Objaverse 1.0 / Sketchfab
Carrot amphora (body) from Traismauer (v 1.0.0)
Scaled 3d-model of a so-called *carrot amphora's body* (Augst 44/Camulodunum 189/Schöne-Mau 15 | type *Bb* & rim *3b1* after Vipard [1995]) found at the *vicus* (civil settlement') of today's Traismauer, which belongs to the former ancient Roman fort of *Augustianis* were auxiliary troops (cavalry) were stationed. The fort was located at the Roman Danube frontier (so-called *limes*) in northeastern Noricum, which is today's Lower Austria. This amphora belongs to a convolute of Roman finds derived from a context excavated in the 1970s. *** # 📍 [Augustianis/Traismauer (Lower Austria)](https://goo.gl/maps/tziQrTZLcvW19fWH6) # *The frament was photogrammetry-scanned & processed & referenced in Agisoft Metashape & assambled & reconstructed in Blender.* * photos: K. Klein * photogrammetry & modeling: D. Hagmann/A. Langendorf --- Vipard, P. (1995). Les amphores carottes (forme Schöne-Mau XV). In: Actes du Congrès de Rouen (51–77) Source: Objaverse 1.0 / Sketchfab
Data from: Mitochondrial gene diversity associated with the atp9 stop codon in natural populations of wild carrot (Daucus carota ssp. carota)
Mitochondrial genomes extracted from wild populations of Daucus carota have been used as a genetic resource by breeders of cultivated carrot, yet little is known concerning the extent of their diversity in nature. Of special interest is a SNP in the putative stop codon of the mitochondrial gene atp9 that has been associated previously with male-sterile and male-fertile phenotypic variants. In this study either sequence or PCR/RFLP genotypes were obtained from the mitochondrial genes atp1, atp9 and cox1 found in D. carota individuals collected from 24 populations in the eastern U.S. More than half of the 128 individuals surveyed had a CAA or AAA, rather than TAA, genotype at the position usually thought to function as an atp9 stop codon in this species. We also found no evidence for mitochondrial RNA editing (Cytosine to Uridine) of the CAA stop codon in either floral or leaf tissue. Evidence for intra-genic recombination, as opposed the more common inter-genic recombination in plant mitochondrial genomes, in our data set is presented. Indel and SNP variants elsewhere in atp9, and in the other two genes surveyed, were non-randomly associated with the three atp9 stop codon variants, though further analysis suggested that multi-locus genotypic diversity had been enhanced by recombination. Overall the mitochondrial genetic diversity was only modestly structured among populations with an Fst of 0.34.
FiO2 and Outcomes After OPCAB (the CARROT Trial)
ClinicalTrials.gov study NCT03945565. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Prophylactic Properties of Carrot Juice in Patients With High-Risk Colorectal Polyps
ClinicalTrials.gov study NCT06335420. IPD Sharing: NO. Countries: 1. Publications: 9.
Data from: Mitochondrial gene diversity associated with the atp9 stop codon in natural populations of wild carrot (Daucus carota ssp. carota)
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Data from: Identification of transcription factor genes involved in anthocyanin biosynthesis in carrot (Daucus carota L.) using RNA-Seq
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Data from: Female monkeys use both the carrot and the stick to promote male participation in intergroup fights
Group-level cooperation often poses a social dilemma in which joint action may be difficult to achieve. Theoretical models and experimental work on humans show that social incentives, such as punishment of defectors and rewarding of cooperators, can promote cooperation in groups of unrelated individuals. Here, we demonstrate that these processes can operate in a non-human animal species, and be used to effectively promote the production of a public good. We took advantage of the fact that intergroup fights in vervet monkeys (Chlorocebus aethiops pygerythrus) are characterized by episodes of intergroup aggression with pauses in-between. During pauses, females selectively groomed males that had participated in the previous aggressive episode, but aggressed male group members that had not. In subsequent (i.e. future) episodes, males who had received either aggression or grooming participated above their personal base-line level. Therefore, female–male aggression and grooming both appear to function as social incentives that effectively promote male participation in intergroup fights. Importantly, females stood to gain much from recruiting males as the probability of winning intergroup fights was dependent on the number of active participants, relative to the number of fighters in the opposing group. Furthermore, females appear to maximize the benefits gained from recruiting males as they primarily used social incentives where and when high-quality food resources, which are the resources primarily limiting to female fitness, were at stake.
DETERMINATION OF VITAMINS IN CARROTS AND THEIR BENEFICIAL EFFECTS ON HUMAN HEALTH
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Data from: Entire plastid phylogeny of the carrot genus (Daucus, Apiaceae): Concordance with nuclear data and mitochondrial and nuclear DNA insertions to the plastid
PREMISE OF THE STUDY: We explored the phylogenetic utility of entire plastid DNA sequences in Daucus and compared the results with prior phylogenetic results using plastid and nuclear DNA sequences. METHODS: We used Illumina sequencing to obtain full plastid sequences of 37 accessions of 20 Daucus taxa and outgroups, analyzed the data with phylogenetic methods, and examined evidence for mitochondrial DNA transfer to the plastid (DcMP). KEY RESULTS: Our phylogenetic trees of the entire data set were highly resolved, with 100% bootstrap support for most of the external and many of the internal clades, except for the clade of D. carota and its most closely related species D. syrticus. Subsets of the data, including regions traditionally used as phylogenetically informative regions, provide various degrees of soft congruence with the entire data set. There are areas of hard incongruence, however, with phylogenies using nuclear data. We extended knowledge of a mitochondrial to plastid DNA insertion sequence previously named DcMP and identified the first instance in flowering plants of a sequence of potential nuclear genome origin inserted into the plastid genome. There is a relationship of inverted repeat junction classes and repeat DNA to phylogeny, but no such relationship with nonsynonymous mutations. CONCLUSIONS: Our data have allowed us to (1) produce a well-resolved plastid phylogeny of Daucus, (2) evaluate subsets of the entire plastid data for phylogeny, (3) examine evidence for plastid and nuclear DNA phylogenetic incongruence, and (4) examine mitochondrial and nuclear DNA insertion into the plastid.
Comparison of Carotenoid Bioavailability From Fresh Papaya, Tomato and Carrot
ClinicalTrials.gov study NCT01748916. IPD Sharing: Not stated. Countries: 2. Publications: 0.
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