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199 results for “plantae”
Fig. 6 in Chemical identification of 18-hydroxycarlactonoic acid as an LjMAX1 product and in planta conversion of its methyl ester to canonical and noncanonical strigolactones in Lotus japonicus
Fig. 6. Conversion of [13C]-CLA to [13C]-5DS and [13C]-18-OH-CLA in the feeding experiment using L. japonicus roots. A) Conversion of [1-13CH]- 3 CLA to [8-13CH]-5DS. LC-MS/MS analysis of [8-13CH]-5DS in root exu3 3 dates after feeding [1-13CH]-CLA. MRM chromatograms (left) and full3 scan spectra of fragment ions (right). The MRM chromatograms of authentic 5DS (red: 331.15/217.00, blue: 331.15/97.00, green: 331.15/ 234.00, m/z in positive mode) and [8-13CH]-5DS (red: 332.15/218.00, 3 blue: 332.15/97.00, green: 332.15/235.00, m/z in positive mode) are shown. B) Conversion of [1-13CH]-CLA to [1-13CH]-18-OH-CLA. LC-MS/ 3 3 MS analysis of [1-13CH]-18-OH-CLA in root exudates after feeding 3 [1-13CH]-CLA. MRM chromatograms (left) and full-scan spectra of frag3 ment ions (right). Authentic 18-OH-CLA was prepared by feeding CL to recombinant Os900. MRM chromatograms of authentic 18-OH-CLA (red: 347.00/303.00, blue: 347.00/113.00, m/z in negative mode) and [1-13CH]-18-OH-CLA (red: 348.00/304.00, blue: 348.00/113.00, m/z in 3 negative mode) are shown. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Chemical identification of 18-hydroxycarlactonoic acid as an LjMAX1 product and in planta conversion of its methyl ester to canonical and noncanonical strigolactones in Lotus japonicus
Fig. 3. Synthetic scheme of 13C-labeled and unlabeled 18-OH-MeCLA. Asterisks indicate the position of 13C.
Fig. 2 in Chemical identification of 18-hydroxycarlactonoic acid as an LjMAX1 product and in planta conversion of its methyl ester to canonical and noncanonical strigolactones in Lotus japonicus
Fig. 2. Detection of 18-hydroxycarlactonoic acid (18-OH-CLA), 4DO and 5DS in CLA feeding experiment by recombinant LjMAX1 and Os900. CLA was incubated with recombinant yeast microsomes. Yeast microsomes having an empty vector and the expression vector pYeDP60-Os900 were used as a negative and a positive control, respectively. The extracts of the microsomes and authentic standard were analyzed by LC-MS/MS. The peak at 7.0 min was presumed to be 18-OH-CLA which may be converted artificially to 4DO and 5DS in the ion source of mass spectrometer, and detected in the MRM transitions for 4DO and 5DS (red: 331.15/216.00, blue: 331.15/97.00, green: 331.15/234.00, m/z in positive mode). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Chemical identification of 18-hydroxycarlactonoic acid as an LjMAX1 product and in planta conversion of its methyl ester to canonical and noncanonical strigolactones in Lotus japonicus
Fig. 1. Detection of carlactonoic acid (CLA), 4-deoxyorobanchol (4DO) and 5- deoxystrigol (5DS) in carlactone (CL) feeding experiment by recombinant Lotus japonicus MAX1 (LjMAX1) and Os900. CL was incubated with yeast microsomes. Yeast microsomes having an empty vector and the expression vector pYeDP60-Os900 were used as a negative and a positive control, respectively. The extracts of the microsomes and authentic standard were analyzed by LCMS/MS. MRM chromatograms of CLA (red: 331.10/69.00, blue: 331.10/ 113.00, m/z in negative mode), 4DO and 5DS (red: 331.15/216.00, blue: 331.15/97.00, green: 331.15/234.00, m/z in positive mode) are shown. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Data from: Legacy of prior host and soil selection on rhizobial fitness in planta
Open the record for dataset details and reuse information.
Data from: Barcoding the kingdom Plantae: new PCR primers for ITS regions of plants with improved universality and specificity
The internal transcribed spacer (ITS) of nuclear ribosomal DNA is one of the most commonly used DNA markers in plant phylogenetic and DNA barcoding analyses, and it has been recommended as a core plant DNA barcode. Despite this popularity, the universality and specificity of PCR primers for the ITS region are not satisfactory, resulting in amplification and sequencing difficulties. By thoroughly surveying and analysing the 18S, 5.8S and 26S sequences of Plantae and Fungi from GenBank, we designed new universal and plant-specific PCR primers for amplifying the whole ITS region and a part of it (ITS1 or ITS2) of plants. In silico analyses of the new and the existing ITS primers based on these highly representative data sets indicated that (i) the newly designed universal primers are suitable for over 95% of plants in most groups; and (ii) the plant-specific primers are suitable for over 85% of plants in most groups without amplification of fungi. A total of 335 samples from 219 angiosperm families, 11 gymnosperm families, 24 fern and lycophyte families, 16 moss families and 17 fungus families were used to test the performances of these primers. In vitro PCR produced similar results to those from the in silico analyses. Our new primer pairs gave PCR improvements up to 30% compared with common-used ones. The new universal ITS primers will find wide application in both plant and fungal biology, and the new plant-specific ITS primers will, by eliminating PCR amplification of nonplant templates, significantly improve the quality of ITS sequence information collections in plant molecular systematics and DNA barcoding.
Diseño de un sistema inteligente de riego para plantas medicinales, aromáticas y condimentarias
<p>Medicinal aromatic and spices plants are present in the expansive majority of Latin American territory due to the traditional medicine that encompasses all of this territory (Bermúdez et al., 2005). Medicinal plants do not require specific care besides humidity and irrigation because these types of plants are in the natural world (Industrial et al., 2005; Molins, 2012). The goal of this work lies in the design of an irrigation system that can be controlling both automatically and manually by sprinkling and dripping that allows the revival of the medicinal aromatic and spices plants both in research and in the application of formal and informal health systems. The design of this system is proposing for the Agroecological farm of the Central University of Valle of Cauca, UCEVA, it has two large units: electric-electronic unit and hydraulic unit. In the first one, a LOGO SIEMENS V8 3.0 PLC and HMI LOGO TDE user interface are used that will be friendly and easy to interact for them. This system includes an extension of digital inputs and outputs that allows it to be scalable that is the number of solenoid valves can be expanding without modifying the electronic systems, only the physical hydraulic systems and the PLC programming software. In addition, the system has an analog signal card that connects humidity, temperature and pH sensors. The main board's electrical grid is single-phase at 110 VAC and its energy demand is supplied by a 450-watt photovoltaic system with a 1000-watt inverter that allows the expansion of the system as its electrical requirements increase. In the second unit, the hydraulic system works by gravity an elevated tank is supplied by a pen-type pump submerged in the farm tank from this two hydraulic lines are taken, one in 4 ”for the drip irrigation system which reduces the distributed valve system (SDV) to ½ '', this system is double in parallel with ball valves and solenoid valves. This valve set consists of 10 normally closed solenoid valves controlled at 110VAC and has a 4 ”water pressure control and flow control valve; the other line leads to the hydroflow system that controls the sprinkler irrigation that is used in the summer season due to the high temperatures that the cultivation of medicinal plants can reach. The design includes the implementation of electrovalves automatically controlled by the PLC with an alternating manual system, in case of failures in the electronic control or maintenance without the need to affect the drip irrigation system. The automatic management of the irrigation of medicinal plants allows this field to resurface as a great bank of medicines to be discovering as a complement to traditional medicine and the basis of preventive medicine (Bermúdez et al., 2005; Industrial et al., 2005).</p>
In vitro vs. In planta: Akanthomyces lecanii compatibility Dataset
<p>In vitro and in planta raw data</p>
Fig. 4. Planta hospedera, Duranta erecta L in Descripción de una nueva especie para el género Macaria (Lepidoptera: Geometridae) y reporte de su planta hospedera en la Argentina
Fig. 4. Planta hospedera, Duranta erecta L. (1758) (Verbenaceae); a) fotografía en floración. b) Ilustración de lámina foliar, se ve reflejado el patrón de alimentación de larvas del quinto estadio. Fig. 4. Host plant, Duranta erecta L. (1758) (Verbenaceae); a) photograph in flowering. b) Illustration of the leaf blade, showing the feeding pattern of fifth instar larvae.
Figura 1 in CArACterístiCAs reprodutiVAs de pLANtAs em florestAs de vegetação costeira tropical do Nordeste do Brasil
Figura 1. Mapa do continente Sul Americano com o Brasil em destaque (cinza escuro), região Nordeste (cinza claro) e Centro de Endemismo Pernambuco (preto), ampliado à direita e com as áreas de restinga estudadas.
Figura 4 in Contribuições e perspectivas da pesquisa brasileira sobre plantas alimentícias silvestres com foco no semiárido
Figura 4. Famílias botânicas com maior quantidade de espécies citadas nos artigos científicos realizados no nordeste brasileiro
Figura 3 in Contribuições e perspectivas da pesquisa brasileira sobre plantas alimentícias silvestres com foco no semiárido
Figura 3. Número de publicações por ano nas bases de dados "Web of Science" e "Scopus", "Food Plants" AND "Wild" no período de 1996 a 2020.
Figura 1 in Contribuições e perspectivas da pesquisa brasileira sobre plantas alimentícias silvestres com foco no semiárido
Figura 1. Estudos realizados no Brasil sobre plantas alimentícias silvestres, encontrados nas bases de dados Web of Science e Scopus.
Figs. 3. A-F in Fenologia, produtividade e qualidade de frutos de jabuticabeiras de diferentes idades das plantas
Figs. 3. A-F. Segunda avaliação do estágio reprodutivo; A. Gemas florais com 12 dias de período reprodutivo; B. Início do florescimento; C. Final da polinização e início do ganho de massa dos frutos; D. frutos verdes; E. frutos verdes e em fase de ganho de massa; F. frutos maduros (safra 2016).
Figs. 2. A-C. A. plantas com tom verde escuro, durante o in Fenologia, produtividade e qualidade de frutos de jabuticabeiras de diferentes idades das plantas
Figs. 2. A-C. A. plantas com tom verde escuro, durante o período chuvoso; B. plantas com folhas maduras; C. plantas com 90 % de desfolha, antes do início do período de irrigação (safra 2015).
Fig. 1 in Fenologia, produtividade e qualidade de frutos de jabuticabeiras de diferentes idades das plantas
Fig. 1. Valores médios de temperatura (°C) e precipitação (mm) mensal em Hidrolândia, Goiás, nos anos de 2015 e 2016.
Fig. 5 in Fenologia, produtividade e qualidade de frutos de jabuticabeiras de diferentes idades das plantas
Fig. 5. Percentagem de queda de frutos de jabuticaba/planta, do início ao final do amadurecimento (safra 2015).
Figs.1 A, B in Trocas gasosas e produtividade de tomateiro com diferentes hastes por planta
Figs.1 A, B. Número de frutos colhidos por planta em cada colheita, em função do número de hastes por planta. A. cultivar Giuliana; B. cultivar Tyna. Tipos de condução: 1. apenas com a haste principal; 2. haste principal + haste secundária emitida imediatamente abaixo do primeiro cacho; 3. as duas primeiras hastes secundárias que surgirem na planta com o desponte da haste principal; 4. as quatro primeiras hastes secundárias que surgirem na planta, com o desponte da haste principal; 5. haste principal e mais três hastes secundárias emitidas abaixo do primeiro cacho.
Fig. 1 in Lista preliminar das plantas alimentícias nativas de Mato Grosso do Sul, Brasil
Fig. 1. Famílias botânicas com maior número de espécies alimentícias (ou com potencial alimentício) no estado de Mato Grosso do Sul.
Figs. 2A-H. A-D. Cabomba furcata. A. planta com folhas submersas e in PLântuLAs e sementes de mAcrófitAs AquáticAs de LAGoAs do PAntAnAL SuL-MAto-Grossense
Figs. 2A-H. A-D. Cabomba furcata. A. planta com folhas submersas e flutuantes sagitadas; B. plântula; C. diásporo; D. semente. E-H. Diodia kuntzei. E. planta; F. plântula; G. diásporo; H. semente. Barras: Figs. A, B, E, F = 1 cm; Fig. C = 2 mm; Figs. D, G, H = 1 mm.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
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