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470 results for “Coffee”
Figure 5 from: Nafisah W, Dalilati AZ, Christina YI, Atho'illah MF, Rifa'ia M, Noor TNETA, Nugraha AP (2024) Amstirdam coffee ameliorates Lp-PLA2 and the inflammatory response in an atherosclerosis rats. Pharmacia 71: 1-8. https://doi.org/10.3897/pharmacia.71.e106817
Figure 5 The effect of ACE increased TGF-β production (CD4+TGF-β+) in mice fed with a high fat-fructose diet for 5 months. The expression of TGF-β (CD4+TGF-β+) of mice fed with HFFD and administration of ACE from flow cytometry analysis (Fig. 5G). The percentage of regulatory (CD4+IL-10+) of mice fed with HFFD and administration of ACE (Fig. 5H). Data are mean ± SD (n=5). N: normal fed mice (non-high fat-fructose diet), HFFD: high fat-fructose diet mice (w/o administration of ACE), D1: HFFD mice receiving ACE 104 mg/kg body weight, D2: HFFD mice receiving ACE 520 mg/kg BW, D3: HFFD mice receiving ACE 5200 mg/kg BW. The different notation on the chart was considered significantly different for each group at p < 0.05 and vice versa on DMRT post hoc test.
Figure 2 from: Nafisah W, Dalilati AZ, Christina YI, Atho'illah MF, Rifa'ia M, Noor TNETA, Nugraha AP (2024) Amstirdam coffee ameliorates Lp-PLA2 and the inflammatory response in an atherosclerosis rats. Pharmacia 71: 1-8. https://doi.org/10.3897/pharmacia.71.e106817
Figure 2 ACE administration reduced foam cells in aorta histopathology (M = 400×) in mice fed a high-fat, high-fructose diet for 5 months. The black arrow shows the accumulation of foam cells in the tunica media, and the asterisk (*) shows the lumen of the aorta. N: normal-fed mice (non-high-fat-fructose diet); HFFD: high-fat-fructose diet mice (w/o administration of ACE); D1: HFFD mice receiving ACE 104 mg/kg body weight; D2: HFFD mice receiving ACE 520 mg/kg body weight; D3: HFFD mice receiving ACE 5200 mg/kg body weight.
Figure 1 from: Nafisah W, Dalilati AZ, Christina YI, Atho'illah MF, Rifa'ia M, Noor TNETA, Nugraha AP (2024) Amstirdam coffee ameliorates Lp-PLA2 and the inflammatory response in an atherosclerosis rats. Pharmacia 71: 1-8. https://doi.org/10.3897/pharmacia.71.e106817
Figure 1 Reduction of Lp-PLA2 production after ACE treatment in mice fed a high-fat, high-fructose diet. The expression of Lp-PLA2 production in mice fed with HFFD and administered ACE was determined from flow cytometry analysis (Fig. 1A). The percentage of Lp-PLA2 production in mice fed with HFFD and administered ACE The data are mean SD (n = 5). N: normal-fed mice (non-high-fat-fructose diet); HFFD: high-fat-fructose diet mice (w/o administration of ACE); D1: HFFD mice receiving ACE 104 mg/kg body weight; D2: HFFD mice receiving ACE 520 mg/gram BW; D3: HFFD mice receiving ACE 5200 mg/kg BW. The different notation on the chart was considered significantly different for each group at p< 0.05 and vice versa on the DMRT post hoc test.
Figure 4 from: Nafisah W, Dalilati AZ, Christina YI, Atho'illah MF, Rifa'ia M, Noor TNETA, Nugraha AP (2024) Amstirdam coffee ameliorates Lp-PLA2 and the inflammatory response in an atherosclerosis rats. Pharmacia 71: 1-8. https://doi.org/10.3897/pharmacia.71.e106817
Figure 4 Administration of ACE increased IL-10 production (CD4+IL-10+) in mice fed with a high-fat, high-fructose diet for 5 months. The expression of CD4+IL-10+ in mice fed with HFFD and administered ACE was determined by flow cytometry analysis (Fig. 4E). The percentage of regulatory cells (CD4+IL-10+) in mice fed with HFFD and administered ACE (Fig. 4F) The data are mean SD (n = 5). N: normal-fed mice (non-high-fat-fructose diet); HFFD: high-fat-fructose diet mice (w/o administration of ACE); D1: HFFD mice receiving ACE 104 mg/kg body weight; D2: HFFD mice receiving ACE 520 mg/kg body weight; D3: HFFD mice receiving ACE 5200 mg/kg body weight. The different notation on the chart was considered significantly different for each group at p < 0.05 and vice versa on the DMRT pos hoc test.
Data for: An aggressive non-consumptive effect mediates pest control and multi-predator interactions in a coffee agroecosystem
<p class="MsoNormal">Natural pest control is an alternative to pesticide use in agriculture, which may help to curb insect declines and promote crop production. Non-consumptive interactions in natural pest control, which historically have received far less attention than consumptive interactions, may have distinct impacts on pest damage suppression and may also mediate positive multi-predator interactions. Additionally, when non-consumptive effects are driven by natural enemy aggression, variation in alternative resources for enemies may impact the strength of pest control. Here we study control of the coffee berry borer (CBB), <em>Hypothenemus hampei</em>, by a keystone arboreal ant species, <em>Azteca sericeasur</em>, which exhibits a non-consumptive effect on CBB by throwing them off coffee plants. We conducted two experiments to investigate: 1) if the strength of this behavior is driven by spatial or temporal variability in scale insect density (an alternative resource which <em>Azteca</em> tends for honeydew), 2) if this behavior mediates positive interactions between <em>Azteca</em> and other ground-foraging ants, and 3) the effect this behavior has on the overall suppression of CBB damage in multi-predator scenarios. Our behavioral experiment showed that nearly all interactions between <em>Azteca</em> and CBB are non-consumptive and that this behavior occurs more frequently in the dry season and with higher densities of scale insects on coffee branches. Our multi-predator experiment revealed that borers thrown off coffee plants by <em>Azteca</em> can survive and potentially damage other nearby plants but may be suppressed by ground-foraging ants. Although we found no non-additive effects between <em>Azteca</em> and ground-foraging ants on overall CBB damage, together, both species resulted in the lowest level of plant damage with the subsequent reduction in "spillover" damage caused by thrown CBB, indicating spatial complementarity between predators. These results present a unique case of natural pest control, where damage suppression is driven almost exclusively by non-consumptive natural enemy aggression, as opposed to consumption or prey behavioral changes. Furthermore, our results demonstrate the variability that may occur in non-consumptive pest control interactions when natural enemy aggressive behavior is impacted by alternative resources, and also show how these non-consumptive effects can mediate positive interactions between natural enemies to enhance overall crop damage reduction.</p>
Application of blender speed control technology in the processing of salak pondoh into coffee in Sibolong Hamlet
<p>Dukuh Sibolong consists of nine RTs with a total population of 672. Based <br> on the information our team got from Mr. Suharno as the head of the hamlet. <br> The hamlet has several groups of informal community organizations such as <br> youth organizations, PKK women. The majority of the population of Sonyo <br> Hamlet are Muslim and have a livelihood as laborers, but there are also those <br> who work as entrepreneurs because the geographical location of Sibolong <br> Hamlet is located in the highlands. Actually, the hamlet of Sibolong has <br> natural potential in the form of Salak Pondoh. One of these has just been <br> processed into salak syrup. The potential of salak is managed by Mr. Suharno. <br> Mr. Suharno has a market opportunity of up to 600 products per month. <br> However, this opportunity brings consequences and problems, namely the <br> wrong seed grinding machine is not owned. Information about some of the <br> problems faced by the zalacca processors must of course be addressed as soon <br> as possible as a solution for developing the zalacca processing business. The <br> team that proposes service as part of the community who happens to be <br> involved in the world of education, feels compelled to help provide solutions <br> to the problems faced by Mr. Suharno's salak processing business. Through <br> this proposed program of science and technology activities and based on the <br> needs analysis that has been carried out, the service team tries to offer <br> solutions to these problems with a touch of science and technology, namely <br> through the main activity of designing a salak seed grinder to make salak <br> coffee. The solosi is used to improve the processing of salak coffee.</p>
Liberica coffee beans thesis
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Coffee table made from recycled Plastic & Wood - a prototype
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Coffee price sales marketing historical record
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FIGURES 14–15 in A new species of myrmecophilous lady beetle in the genus Diomus (Coleoptera: Coccinellidae: Diomini) from Chiapas, Mexico that feeds on green coffee scale, Coccus viridis (Green) (Hemiptera: Coccidae)
FIGURES 14–15. Mature larva of D. lupusapudoves: 14, dorsal view; 15, ventral view.
FIGURE 1 in New species and records of earthworms (Annelida, Oligochaeta) in plantain cropping systems in Colombia's coffee-growing region
FIGURE 1. Distribution of farms in Quindío department, Colombia.
Figure 1 in Genetic diversity of Arabica coffee (Coffea arabica L.) collections
Figure 1. Diversity of Arabica coffee individuals based on the first and second components of PCA.
Figure 9 in The coffee leaf miner, Leucoptera coffeella (Lepidoptera: Lyonetiidae): identification of the larval instars and description of male and female genitalia
Figure 9 Leucoptera coffeella, female genitalia. (A) Ovipositor ventral view. Arrow indicates ovipositor lobe. (B) Sclerite ventral view. Arrow indicates the sclerite's concave end. (C) Corpus bursae ventral view. Arrow indicates spines.
Figure 5 in The coffee leaf miner, Leucoptera coffeella (Lepidoptera: Lyonetiidae): identification of the larval instars and description of male and female genitalia
Figure 5 Leucoptera coffeella, adult male. (A) Male ventral view. White-colored body scales. (B) Male dorsal view. Apex of the wings with black dots surrounded by yellow scales, with a "V" shape facing the posterior region of the body.
Figure 8 in The coffee leaf miner, Leucoptera coffeella (Lepidoptera: Lyonetiidae): identification of the larval instars and description of male and female genitalia
Figure 8 Leucoptera coffeella, adult female. (A) Female ventral view.(B) Female dorsal view. Arrow indicates the apex of the abdomen with a "C" shape facing the anterior region of the body.
Figure 1 in The coffee leaf miner, Leucoptera coffeella (Lepidoptera: Lyonetiidae): identification of the larval instars and description of male and female genitalia
Figure 1 States of Brazil with the incidence of Leucoptera coffeella (red dots). Rondônia (RO), Mato Grosso (MT), Pará (PA), Goiás (GO), Distrito Federal (DF), Bahia (BA), Minas Gerais (MG), Espírito Santo (ES), São Paulo (SP), Rio de Janeiro (RJ), Paraná (PR), Santa Catarina (SC).
Figure 4 in First Record of the Coffee Berry Borer, Hypothenemus hampei (Ferrari, 1867), on the Hawaiian Island of Lanai (Coleoptera: Curculionidae: Scolytinae)
Figure 4. View of a section of Kapano Gulch, with feral coffee, Coffea arabica L., visible (center and left), September 2020. Photograph by Kari K. Bogner.
Figure 5 in First Report of Exploitation of Coffee Beans by Black Twig Borer (Xylosandrus Compactus) and Tropical Nut Borer (Hypothenemus obscurus) (Coleoptera; Curculionidae: Scolytinae) in Hawaii
Figure 5. Damage of Hypothenemus obscurus to coffee berries. Holes were observed around the blossom area or on the side of the berry (A, left) and sometimes holes were observed reaching the endosperm (B, right).
Figure 1 in First Report of Exploitation of Coffee Beans by Black Twig Borer (Xylosandrus Compactus) and Tropical Nut Borer (Hypothenemus obscurus) (Coleoptera; Curculionidae: Scolytinae) in Hawaii
Figure 1. Dorsal view of adults of Xylosandrus compactus (A, left) and Hypothenemus obscurus (B, right).
Fig. 5 in Diversity of anurans in forest fragments of southwestern Ethiopia: The case of the Yayu Coffee Forest Biosphere Reserve (YCFBR)
Fig. 5. Selected species encountered in YCFBR. (A) Leptopelis ragazzii, (B) Paracassina obscura, (C) Hyperolius nasutus, (D) Xenopus clivii, (E) Ptychadena anchiatae, (F) Conraua beccarii.
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