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cuprina</title> <meta name="description" content="Search results for: Lucilia cuprina"> <meta name="keywords" content="Lucilia cuprina"> <meta name="viewport" content="width=device-width, initial-scale=1, minimum-scale=1, maximum-scale=1, user-scalable=no"> <meta charset="utf-8"> <link href="https://cdn.waset.org/favicon.ico" type="image/x-icon" rel="shortcut icon"> <link href="https://cdn.waset.org/static/plugins/bootstrap-4.2.1/css/bootstrap.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/plugins/fontawesome/css/all.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/css/site.css?v=150220211555" rel="stylesheet"> </head> <body> <header> <div class="container"> <nav class="navbar navbar-expand-lg navbar-light"> <a class="navbar-brand" href="https://waset.org"> <img src="https://cdn.waset.org/static/images/wasetc.png" alt="Open Science Research Excellence" title="Open Science Research Excellence" /> </a> <button class="d-block d-lg-none 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action="https://publications.waset.org/abstracts/search"> <div id="custom-search-input"> <div class="input-group"> <i class="fas fa-search"></i> <input type="text" class="search-query" name="q" placeholder="Author, Title, Abstract, Keywords" value="Lucilia cuprina"> <input type="submit" class="btn_search" value="Search"> </div> </div> </form> </div> </div> <div class="row mt-3"> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 13</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: Lucilia cuprina</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13</span> The Toxicity Effects of HICIDE VD-9 on the Mortality of Lucilia cuprina under Laboratory Conditions</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mehdi%20Shahmoradi%20Moghadam">Mehdi Shahmoradi Moghadam</a>, <a href="https://publications.waset.org/abstracts/search?q=Saba%20Kavian"> Saba Kavian</a>, <a href="https://publications.waset.org/abstracts/search?q=Mehdi%20Zabihzadeh"> Mehdi Zabihzadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Amir%20Mohammad%20Alborzi"> Amir Mohammad Alborzi</a>, <a href="https://publications.waset.org/abstracts/search?q=Reza%20Sadeghi"> Reza Sadeghi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Cypermethrin is one of the most widely used synthetic insecticides to control pests in veterinary, industrial and agricultural environments. In the present study, the mortalities of Lucilia Cuprina as the key pest of meat were studied after being exposed to HICIDE VD-9 (a ready-to-use disinfectant/insecticide containing cypermethrin, polyhexanide and quaternary ammonium compounds produced by Dana pharmed lotus Co., Iran) within 15 minutes. The experimental results showed that moralities percentage of egg, larvae and adults of Lucilia Cuprina were 48%, 81% and 70%, respectively. Based on the obtained results, it can be predicted that in addition to controlling the insect pests of blow flies, HICIDE VD-9, as a cost-effective and environmentally friendly disinfectant/insecticide, can be effective against other insects, e.g., biting flies, fleas, midges, mosquitoes and ticks. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cypermethrin" title="cypermethrin">cypermethrin</a>, <a href="https://publications.waset.org/abstracts/search?q=HICIDE%20VD-9" title=" HICIDE VD-9"> HICIDE VD-9</a>, <a href="https://publications.waset.org/abstracts/search?q=Lucilia%20cuprina" title=" Lucilia cuprina"> Lucilia cuprina</a>, <a href="https://publications.waset.org/abstracts/search?q=mortality" title=" mortality"> mortality</a>, <a href="https://publications.waset.org/abstracts/search?q=toxicity" title=" toxicity"> toxicity</a> </p> <a href="https://publications.waset.org/abstracts/176093/the-toxicity-effects-of-hicide-vd-9-on-the-mortality-of-lucilia-cuprina-under-laboratory-conditions" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/176093.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">110</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">12</span> Insect Cell-Based Models: Asutralian Sheep bBlowfly Lucilia Cuprina Embryo Primary Cell line Establishment and Transfection</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Yunjia%20Yang">Yunjia Yang</a>, <a href="https://publications.waset.org/abstracts/search?q=Peng%20Li"> Peng Li</a>, <a href="https://publications.waset.org/abstracts/search?q=Gordon%20Xu"> Gordon Xu</a>, <a href="https://publications.waset.org/abstracts/search?q=Timothy%20Mahony"> Timothy Mahony</a>, <a href="https://publications.waset.org/abstracts/search?q=Bing%20Zhang"> Bing Zhang</a>, <a href="https://publications.waset.org/abstracts/search?q=Neena%20Mitter"> Neena Mitter</a>, <a href="https://publications.waset.org/abstracts/search?q=Karishma%20Mody"> Karishma Mody</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Sheep flystrike is one of the most economically important diseases affecting the Australian sheep and wool industry (>356M/annually). Currently, control of Lucillia cuprina relies almost exclusively on chemicals controls, and the parasite has developed resistance to nearly all control chemicals used in the past. It is, therefore, critical to develop an alternative solution for the sustainable control and management of flystrike. RNA interference (RNAi) technologies have been successfully explored in multiple animal industries for developing parasites controls. This research project aims to develop a RNAi based biological control for sheep blowfly. Double-stranded RNA (dsRNA) has already proven successful against viruses, fungi, and insects. However, the environmental instability of dsRNA is a major bottleneck for successful RNAi. Bentonite polymer (BenPol) technology can overcome this problem, as it can be tuned for the controlled release of dsRNA in the gut challenging pH environment of the blowfly larvae, prolonging its exposure time to and uptake by target cells. To investigate the potential of BenPol technology for dsRNA delivery, four different BenPol carriers were tested for their dsRNA loading capabilities, and three of them were found to be capable of affording dsRNA stability under multiple temperatures (4°C, 22°C, 40°C, 55°C) in sheep serum. Based on stability results, dsRNA from potential targeted genes was loaded onto BenPol carriers and tested in larvae feeding assays, three genes resulting in knockdowns. Meanwhile, a primary blowfly embryo cell line (BFEC) derived from L. cuprina embryos was successfully established, aim for an effective insect cell model for testing RNAi efficacy for preliminary assessments and screening. The results of this study establish that the dsRNA is stable when loaded on BenPol particles, unlike naked dsRNA rapidly degraded in sheep serum. The stable nanoparticle delivery system offered by BenPol technology can protect and increase the inherent stability of dsRNA molecules at higher temperatures in a complex biological fluid like serum, providing promise for its future use in enhancing animal protection. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=lucilia%20cuprina" title="lucilia cuprina">lucilia cuprina</a>, <a href="https://publications.waset.org/abstracts/search?q=primary%20cell%20line%20establishment" title=" primary cell line establishment"> primary cell line establishment</a>, <a href="https://publications.waset.org/abstracts/search?q=RNA%20interference" title=" RNA interference"> RNA interference</a>, <a href="https://publications.waset.org/abstracts/search?q=insect%20cell%20transfection" title=" insect cell transfection"> insect cell transfection</a> </p> <a href="https://publications.waset.org/abstracts/163966/insect-cell-based-models-asutralian-sheep-bblowfly-lucilia-cuprina-embryo-primary-cell-line-establishment-and-transfection" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/163966.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">73</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">11</span> Molecular Identification and Evolutionary Status of Lucilia bufonivora: An Obligate Parasite of Amphibians in Europe</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Gerardo%20Arias">Gerardo Arias</a>, <a href="https://publications.waset.org/abstracts/search?q=Richard%20Wall"> Richard Wall</a>, <a href="https://publications.waset.org/abstracts/search?q=Jamie%20Stevens"> Jamie Stevens</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Lucilia bufonivora Moniez, is an obligate parasite of toads and frogs widely distributed in Europe. Its sister taxon Lucilia silvarum Meigen behaves mainly as a carrion breeder in Europe, however it has been reported as a facultative parasite of amphibians. These two closely related species are morphologically almost identical, which has led to misidentification, and in fact, it has been suggested that the amphibian myiasis cases by L. silvarum reported in Europe should be attributed to L. bufonivora. Both species remain poorly studied and their taxonomic relationships are still unclear. The identification of the larval specimens involved in amphibian myiasis with molecular tools and phylogenetic analysis of these two closely related species may resolve this problem. In this work seventeen unidentified larval specimens extracted from toad myiasis cases of the UK, the Netherlands and Switzerland were obtained, their COX1 (mtDNA) and EF1-α (Nuclear DNA) gene regions were amplified and then sequenced. The 17 larval samples were identified with both molecular markers as L. bufonivora. Phylogenetic analysis was carried out with 10 other blowfly species, including L. silvarum samples from the UK and USA. Bayesian Inference trees of COX1 and a combined-gene dataset suggested that L. silvarum and L. bufonivora are separate sister species. However, the nuclear gene EF1-α does not appear to resolve their relationships, suggesting that the rates of evolution of the mtDNA are much faster than those of the nuclear DNA. This work provides the molecular evidence for successful identification of L. bufonivora and a molecular analysis of the populations of this obligate parasite from different locations across Europe. The relationships with L. silvarum are discussed. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=calliphoridae" title="calliphoridae">calliphoridae</a>, <a href="https://publications.waset.org/abstracts/search?q=molecular%20evolution" title=" molecular evolution"> molecular evolution</a>, <a href="https://publications.waset.org/abstracts/search?q=myiasis" title=" myiasis"> myiasis</a>, <a href="https://publications.waset.org/abstracts/search?q=obligate%20parasitism" title=" obligate parasitism"> obligate parasitism</a> </p> <a href="https://publications.waset.org/abstracts/77861/molecular-identification-and-evolutionary-status-of-lucilia-bufonivora-an-obligate-parasite-of-amphibians-in-europe" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/77861.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">242</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">10</span> Development of a Stable RNAi-Based Biological Control for Sheep Blowfly Using Bentonite Polymer Technology</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Yunjia%20Yang">Yunjia Yang</a>, <a href="https://publications.waset.org/abstracts/search?q=Peng%20Li"> Peng Li</a>, <a href="https://publications.waset.org/abstracts/search?q=Gordon%20Xu"> Gordon Xu</a>, <a href="https://publications.waset.org/abstracts/search?q=Timothy%20Mahony"> Timothy Mahony</a>, <a href="https://publications.waset.org/abstracts/search?q=Bing%20Zhang"> Bing Zhang</a>, <a href="https://publications.waset.org/abstracts/search?q=Neena%20Mitter"> Neena Mitter</a>, <a href="https://publications.waset.org/abstracts/search?q=Karishma%20Mody"> Karishma Mody</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Sheep flystrike is one of the most economically important diseases affecting the Australian sheep and wool industry (>356M/annually). Currently, control of Lucillia cuprina relies almost exclusively on chemicals controls and the parasite has developed resistance to nearly all control chemicals used in the past. It is therefore critical to develop an alternative solution for the sustainable control and management of flystrike. RNA interference (RNAi) technologies have been successfully explored in multiple animal industries for developing parasites controls. This research project aims to develop a RNAi based biological control for sheep blowfly. Double-stranded RNA (dsRNA) has already proven successful against viruses, fungi and insects. However, the environmental instability of dsRNA is a major bottleneck for successful RNAi. Bentonite polymer (BenPol) technology can overcome this problem, as it can be tuned for the controlled release of dsRNA in the gut challenging pH environment of the blowfly larvae, prolonging its exposure time to and uptake by target cells. To investigate the potential of BenPol technology for dsRNA delivery, four different BenPol carriers were tested for their dsRNA loading capabilities, and three of them were found to be capable of affording dsRNA stability under multiple temperatures (4°C, 22°C, 40°C, 55°C) in sheep serum. Based on stability results, dsRNA from potential targeted genes was loaded onto BenPol carriers and tested in larvae feeding assays, three genes resulting in knockdowns. Meanwhile, a primary blowfly embryo cell line (BFEC) derived from L. cuprina embryos was successfully established, aim for an effective insect cell model for testing RNAi efficacy for preliminary assessments and screening. The results of this study establish that the dsRNA is stable when loaded on BenPol particles, unlike naked dsRNA rapidly degraded in sheep serum. The stable nanoparticle delivery system offered by BenPol technology can protect and increase the inherent stability of dsRNA molecules at higher temperatures in a complex biological fluid like serum, providing promise for its future use in enhancing animal protection. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=flystrike" title="flystrike">flystrike</a>, <a href="https://publications.waset.org/abstracts/search?q=RNA%20interference" title=" RNA interference"> RNA interference</a>, <a href="https://publications.waset.org/abstracts/search?q=bentonite%20polymer%20technology" title=" bentonite polymer technology"> bentonite polymer technology</a>, <a href="https://publications.waset.org/abstracts/search?q=Lucillia%20cuprina" title=" Lucillia cuprina"> Lucillia cuprina</a> </p> <a href="https://publications.waset.org/abstracts/164122/development-of-a-stable-rnai-based-biological-control-for-sheep-blowfly-using-bentonite-polymer-technology" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/164122.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">92</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">9</span> Application of Forensic Entomology to Estimate the Post Mortem Interval</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Meriem%20Taleb">Meriem Taleb</a>, <a href="https://publications.waset.org/abstracts/search?q=Ghania%20Tail"> Ghania Tail</a>, <a href="https://publications.waset.org/abstracts/search?q=Fatma%20Zohra%20Kara"> Fatma Zohra Kara</a>, <a href="https://publications.waset.org/abstracts/search?q=Brahim%20Djedouani"> Brahim Djedouani</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20Moussa"> T. Moussa</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Forensic entomology has grown immensely as a discipline in the past thirty years. The main purpose of forensic entomology is to establish the post mortem interval or PMI. Three days after the death, insect evidence is often the most accurate and sometimes the only method of determining elapsed time since death. This work presents the estimation of the PMI in an experiment to test the reliability of the accumulated degree days (ADD) method and the application of this method in a real case. The study was conducted at the Laboratory of Entomology at the National Institute for Criminalistics and Criminology of the National Gendarmerie, Algeria. The domestic rabbit Oryctolagus cuniculus L. was selected as the animal model. On 08th July 2012, the animal was killed. Larvae were collected and raised to adulthood. Estimation of oviposition time was calculated by summing up average daily temperatures minus minimum development temperature (also specific to each species). When the sum is reached, it corresponds to the oviposition day. Weather data were obtained from the nearest meteorological station. After rearing was accomplished, three species emerged: Lucilia sericata, Chrysomya albiceps, and Sarcophaga africa. For Chrysomya albiceps species, a cumulation of 186°C is necessary. The emergence of adults occured on 22nd July 2012. A value of 193.4°C is reached on 9th August 2012. Lucilia sericata species require a cumulation of 207°C. The emergence of adults occurred on 23rd, July 2012. A value of 211.35°C is reached on 9th August 2012. We should also consider that oviposition may occur more than 12 hours after death. Thus, the obtained PMI is in agreement with the actual time of death. We illustrate the use of this method during the investigation of a case of a decaying human body found on 03rd March 2015 in Bechar, South West of Algerian desert. Maggots were collected and sent to the Laboratory of Entomology. Lucilia sericata adults were identified on 24th March 2015 after emergence. A sum of 211.6°C was reached on 1st March 2015 which corresponds to the estimated day of oviposition. Therefore, the estimated date of death is 1st March 2015 ± 24 hours. The estimated PMI by accumulated degree days (ADD) method seems to be very precise. Entomological evidence should always be used in homicide investigations when the time of death cannot be determined by other methods. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=forensic%20entomology" title="forensic entomology">forensic entomology</a>, <a href="https://publications.waset.org/abstracts/search?q=accumulated%20degree%20days" title=" accumulated degree days"> accumulated degree days</a>, <a href="https://publications.waset.org/abstracts/search?q=postmortem%20interval" title=" postmortem interval"> postmortem interval</a>, <a href="https://publications.waset.org/abstracts/search?q=diptera" title=" diptera"> diptera</a>, <a href="https://publications.waset.org/abstracts/search?q=Algeria" title=" Algeria"> Algeria</a> </p> <a href="https://publications.waset.org/abstracts/34231/application-of-forensic-entomology-to-estimate-the-post-mortem-interval" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/34231.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">294</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">8</span> Lucilia Sericata Netrin-A: Secreted by Salivary Gland Larvae as a Potential to Neuroregeneration</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hamzeh%20Alipour">Hamzeh Alipour</a>, <a href="https://publications.waset.org/abstracts/search?q=Masoumeh%20Bagheri"> Masoumeh Bagheri</a>, <a href="https://publications.waset.org/abstracts/search?q=Tahereh%20Karamzadeh"> Tahereh Karamzadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Abbasali%20Raz"> Abbasali Raz</a>, <a href="https://publications.waset.org/abstracts/search?q=Kourosh%20Azizi"> Kourosh Azizi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Netrin-A, a protein identified for conducting commissural axons, has a similar role in angiogenesis. In addition, studies have shown that one of the netrin-A receptors is expressed in the growing cells of small capillaries. It will be interesting to study this new group of molecules because their role in wound healing will become clearer in the future due to angiogenesis. The greenbottle blowfly Luciliasericata (L. sericata) larvae are increasingly used in maggot therapy of chronic wounds. This aim of this was the identification of moleculareatures of Netrin-A in L. sericata larvae. Larvae were reared under standard maggotarium conditions. The nucleic acid sequence of L. sericataNetrin-A (LSN-A) was then identified using Rapid Amplification of cDNA Ends (RACE) and Rapid Amplification of Genomic Ends (RAGE). Parts of the Netrin-A gene, including the middle, 3′-, and 5′-ends were identified, TA cloned in pTG19 plasmid, and transferred into DH5ɑ Escherichia coli. Each part was sequenced and assembled using SeqMan software. This gene structure was further subjected to in silico analysis. The DNA of LSN-A was identified to be 2407 bp, while its mRNA sequence was recognized as 2115 bp by Oligo0.7 software. It translated the Netrin-A protein with 704 amino acid residues. Its molecular weight is estimated to be 78.6 kDa. The 3-D structure ofNetrin-A drawn by SWISS-MODEL revealed its similarity to the Netrin-1 of humans with 66.8% identity. The LSN-A protein conduces to repair the myelin membrane in neuronal cells. Ultimately, it can be an effective candidate in neural regeneration and wound healing. Furthermore, our next attempt is to deplore recombinant proteins for use in medical sciences. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=maggot%20therapy" title="maggot therapy">maggot therapy</a>, <a href="https://publications.waset.org/abstracts/search?q=netrin-A" title=" netrin-A"> netrin-A</a>, <a href="https://publications.waset.org/abstracts/search?q=RACE" title=" RACE"> RACE</a>, <a href="https://publications.waset.org/abstracts/search?q=RAGE" title=" RAGE"> RAGE</a>, <a href="https://publications.waset.org/abstracts/search?q=lucilia%20sericata" title=" lucilia sericata"> lucilia sericata</a> </p> <a href="https://publications.waset.org/abstracts/156855/lucilia-sericata-netrin-a-secreted-by-salivary-gland-larvae-as-a-potential-to-neuroregeneration" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/156855.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">109</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">7</span> Patchwork City: An Affective Map for a Patchwork Zone</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Maria%20Luc%C3%ADlia%20Borges">Maria Lucília Borges</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This article presents the creation and design process of the "patchwork map" made for the project “Santo Amaro em Rede” (Santo Amaro on Web). The project was carried out in 2009 by SESC – SP – Brazil (Social Service for the Commerce of São Paulo) in partnership with Instituto Pólis. It is a mapping of socio-cultural dynamics of São Paulo’s South Zone and neighboring municipalities. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=affective%20map" title="affective map">affective map</a>, <a href="https://publications.waset.org/abstracts/search?q=cartography" title=" cartography"> cartography</a>, <a href="https://publications.waset.org/abstracts/search?q=S%C3%A3o%20Paulo%20city" title=" São Paulo city"> São Paulo city</a>, <a href="https://publications.waset.org/abstracts/search?q=space" title=" space"> space</a>, <a href="https://publications.waset.org/abstracts/search?q=patchwork" title=" patchwork"> patchwork</a> </p> <a href="https://publications.waset.org/abstracts/27660/patchwork-city-an-affective-map-for-a-patchwork-zone" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/27660.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">380</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">6</span> Attraction and Identification of Early Scavenger Insects on Shaded and Sunny Liver Baits in a Saharian Region of South-Central Algeria </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20M.%20Taleb">A. M. Taleb</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20G.%20Tail"> A. G. Tail</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20F.%20Kara"> A. F. Kara</a>, <a href="https://publications.waset.org/abstracts/search?q=B.%20B.%20Djedouani"> B. B. Djedouani</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20T.%20Moussa"> C. T. Moussa </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Forensic entomology is the use of insects to aid legal investigations. The main purpose of forensic entomology is to establish the postmortem interval (PMI). In order to estimate the PMI, a forensic entomologist compares the case data with certain reference information relevant to the particular location and time of year. This reference information, including the local distribution of species, are not available in Algeria. Therefore, experiments need to be conducted to provide references for entomological evidence. The objective of this study was to identify the necrophagous flies species which arrive first to carrion using liver baits in Ghardaia, South Algeria. The study was carried out during the spring season in the palmeral of Beni Isguen, Ghardaia which is well known by its hot arid climate. The experiment site (32°28’0’’ N, 3°42’0’’ E), is situated at an altitude of about 526 metres above mean sea level. On April the 4th, 2014, a number of three replicates of liver baited traps were placed in the shade and other three baits were exposed to the sun. Flying insects and larvae were captured and identified. After few minutes, flies invaded the traps which were exposed to the sun. In contrast, no flies were observed in the other traps. A total number of fourty five (45) adult specimens belonging to three taxa were identified: Calliphora vicina (Robineau-Desvoidy, 1830) (Diptera, Calliphoridae) (51.11 %), Lucilia sericata (Meigen, 1826) (Diptera, Calliphoridae) (33.33 %) and Sarcophaga africa (Wiedemann, 1824) (Diptera: Sarcophagidae) (15.55 %). Six hundred and three (603) maggots belonging to two taxa were identified: Calliphora vicina (76.28 %) and Lucilia sericata (23.71 %). The data obtained from this study provides baseline information regarding the carrion fauna of this area. It will also form a basis for similar studies in different geographical and climatological regions of Algeria. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=forensic%20entomology" title="forensic entomology">forensic entomology</a>, <a href="https://publications.waset.org/abstracts/search?q=liver%20baits" title=" liver baits"> liver baits</a>, <a href="https://publications.waset.org/abstracts/search?q=necrophagous%20fly" title=" necrophagous fly"> necrophagous fly</a>, <a href="https://publications.waset.org/abstracts/search?q=Ghardaia" title=" Ghardaia"> Ghardaia</a>, <a href="https://publications.waset.org/abstracts/search?q=South%20Algeria" title=" South Algeria"> South Algeria</a> </p> <a href="https://publications.waset.org/abstracts/34578/attraction-and-identification-of-early-scavenger-insects-on-shaded-and-sunny-liver-baits-in-a-saharian-region-of-south-central-algeria" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/34578.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">366</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">5</span> Enhancing Animal Protection: Topical RNAi with Polymer Carriers for Sustainable Animal Health in Australian Sheep Flystrike</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Yunjia%20Yang">Yunjia Yang</a>, <a href="https://publications.waset.org/abstracts/search?q=Yakun%20Yan"> Yakun Yan</a>, <a href="https://publications.waset.org/abstracts/search?q=Peng%20Li"> Peng Li</a>, <a href="https://publications.waset.org/abstracts/search?q=Gordon%20Xu"> Gordon Xu</a>, <a href="https://publications.waset.org/abstracts/search?q=Timothy%20Mahony"> Timothy Mahony</a>, <a href="https://publications.waset.org/abstracts/search?q=Neena%20Mitter"> Neena Mitter</a>, <a href="https://publications.waset.org/abstracts/search?q=Karishma%20Mody"> Karishma Mody</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Sheep flystrike is one of the most economically important diseases affecting the Australian sheep and wool industry (>356M/annually). Currently, control of Lucillia cuprina relies almost exclusively on chemicals controls and the parasite has developed resistance to nearly all control chemicals used in the past. It is therefore critical to develop an alternative solution for the sustainable control and management of flystrike. RNA interference (RNAi) technologies have been successfully explored in multiple animal industries for developing parasites controls. This research project aims to develop a RNAi based biological control for sheep blowfly. Double-stranded RNA (dsRNA) has already proven successful against viruses, fungi and insects. However, the environmental instability of dsRNA is a major bottleneck with a protection window only lasting 5-7 days. Bentonite polymer (BenPol) technology can overcome this problem, as it can be tuned for controlled release of the dsRNA in the gut challenging pH environment of the blowfly larvae, prolonging its exposure time to and uptake by target cells. We have investigated four different BenPol carriers for their dsRNA loading capabilities of which three of them were able to afford dsRNA stability under multiple temperatures (4°C, 22°C, 40°C, 55°C) in the sheep serum. Based on stability results, we further tested dsRNA from potential targeted genes loaded with BenPol carrier in larvae feeding assay, and get three knockdowns. Our results, establish that the dsRNA when loaded on BenPol particles is stable unlike naked dsRNA which is rapidly degraded in the sheep serum. A stable nanoparticles delivery system that can protect and increase the inherent stability of the dsRNA molecules at higher temperatures in a complex biological fluid like serum, offers a great deal of promise for the future use of this approach for enhancing animal protection. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=RNA%20interference" title="RNA interference">RNA interference</a>, <a href="https://publications.waset.org/abstracts/search?q=Lucillia%20cuprina" title=" Lucillia cuprina"> Lucillia cuprina</a>, <a href="https://publications.waset.org/abstracts/search?q=polymer%20carriers" title=" polymer carriers"> polymer carriers</a>, <a href="https://publications.waset.org/abstracts/search?q=polymer%20stability" title=" polymer stability"> polymer stability</a> </p> <a href="https://publications.waset.org/abstracts/163869/enhancing-animal-protection-topical-rnai-with-polymer-carriers-for-sustainable-animal-health-in-australian-sheep-flystrike" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/163869.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">81</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4</span> Isolation, Characterization, and Antibacterial Evaluation of Antimicrobial Peptides and Derivatives from Fly Larvae Sarconesiopsis magellanica (Diptera: Calliphoridae)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20D%C3%ADaz-Roa">A. Díaz-Roa</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20I.%20Silva%20Junior"> P. I. Silva Junior</a>, <a href="https://publications.waset.org/abstracts/search?q=F.%20J.%20Bello"> F. J. Bello</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Sarconesiopsis magellanica (Diptera: Calliphoridae) is a medically important necrophagous fly which is used for establishing the post-mortem interval. Dipterous maggots release diverse proteins and peptides contained in larval excretion and secretion (ES) products playing a key role in digestion. The most important mechanism for combating infection using larval therapy depends on larval ES. These larvae are protected against infection by a diverse spectrum of antimicrobial peptides (AMPs), one already known like lucifensin. Special interest in these peptides has also been aroused regarding understanding their role in wound healing since they degrade necrotic tissue and kill different bacteria during larval therapy. The action of larvae on wounds occurs through 3 mechanisms of action: removal of necrotic tissue, stimulation of granulation tissue, and antibacterial action of larval ES. Some components of the ES include calcium, urea, allantoin ammonium bicarbonate and reducing the viability of Gram positive and Gram negative bacteria. The Lucilia sericata fly larvae have been the most used, however, we need to evaluate new species that could potentially be similar or more effective than fly above. This study was thus aimed at identifying and characterizing S. magellanica AMPs contained in ES products for the first time and compared them with the common fly used L. sericata. These products were obtained from third-instar larvae taken from a previously established colony. For the first analysis, ES fractions were separate by Sep-Pak C18 disposable columns (first step). The material obtained was fractionated by RP-HPLC by using Júpiter C18 semi-preparative column. The products were then lyophilized and their antimicrobial activity was characterized by incubation with different bacterial strains. The first chromatographic analysis of ES from L. sericata gives 6 fractions with antimicrobial activity against Gram-positive bacteria Micrococus luteus, and 3 fractions with activity against Gram-negative bacteria Pseudomonae aeruginosa while the one from S. magellanica gaves 1 fraction against M. luteus and 4 against P. aeruginosa. Maybe one of these fractions could correspond to the peptide already known from L. sericata. These results show the first work for supporting further experiments aimed at validating S. magellanica use in larval therapy. We still need to search if we find some new molecules, by making mass spectrometry and ‘de novo sequencing’. Further studies are necessary to identify and characterize them to better understand their functioning. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=antimicrobial%20peptides" title="antimicrobial peptides">antimicrobial peptides</a>, <a href="https://publications.waset.org/abstracts/search?q=larval%20therapy" title=" larval therapy"> larval therapy</a>, <a href="https://publications.waset.org/abstracts/search?q=Lucilia%20sericata" title=" Lucilia sericata"> Lucilia sericata</a>, <a href="https://publications.waset.org/abstracts/search?q=Sarconesiopsis%20magellanica" title=" Sarconesiopsis magellanica"> Sarconesiopsis magellanica</a> </p> <a href="https://publications.waset.org/abstracts/34404/isolation-characterization-and-antibacterial-evaluation-of-antimicrobial-peptides-and-derivatives-from-fly-larvae-sarconesiopsis-magellanica-diptera-calliphoridae" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/34404.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">367</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">3</span> Species Diversity of Coleoptera (Insecta: Coleoptera) Damaging Saxaul (Chenopodiáceae: Haloxylon spp.) in the Deserts Area of South-East Kazakhstan</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=B.%20Mombayeva">B. Mombayeva</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In the deserts area of south east of Kazakhstan, 16 species of Coleoptera from 6 families and 12 genus of insects damaging Saxaul have been revealed. The vast number of species belong to the Cerambycidae familyCapricorn Beetle (4 species) and Hemlock Borer of Melanophila genus and 3 species of weevils and flea-beetles, and 1 species of coctsinelids and carrion beetle. Some of them cause appreciable harm, and sometimes very heavy damageto saxaul. According to food specialization they are divided into polyphages and - oligophages. According to the confinement to saxaul parts, registered beetles insects mainly feed on generative parts (11 species) and leaves (5 species). 9 species from them feed on roots, leaves and generative organs. They are scarablike beetle’s larvae (Apatophysismongolica Semenov., Tursmenigenavarentzovi Melg., Phytoecia (Opsilla) coerulescens Scopoli., Apatophysismongolica Semenov.), Jewel beetles (Julodis (s. Str.) Variolaris (Pallas), Sphenoptera (s. Str.) cuprina Motschulsky, S. (s. str.) exarata (Fischer), SphenopterapotaniniJak.) and some weevil (Barisartemisiae Hbst.). The larvae eat the roots and the imago - generative organs. Their feeding noticeably has its effect on the condition of saxaul. Beetles also slightlygnaw vegetative organs of plants. Among the harmful species the desert Capricorn Beetle Julodisvariolaris (Pallas) deserved attention. Its larvae live in the soil and cause harm to the roots of Saxaul and other pasture plants. In addition, the larvae of Sphenopterapotanini, S.punctatissima colonize the roots, trunk and branches of Haloxylon. In the spring Saxaul flowers are much damaged by Ladybeetle Bulaealichatchovi. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=saxaul" title="saxaul">saxaul</a>, <a href="https://publications.waset.org/abstracts/search?q=coleoptera" title=" coleoptera"> coleoptera</a>, <a href="https://publications.waset.org/abstracts/search?q=insecta" title=" insecta"> insecta</a>, <a href="https://publications.waset.org/abstracts/search?q=haloxylon" title=" haloxylon"> haloxylon</a> </p> <a href="https://publications.waset.org/abstracts/33303/species-diversity-of-coleoptera-insecta-coleoptera-damaging-saxaul-chenopodiaceae-haloxylon-spp-in-the-deserts-area-of-south-east-kazakhstan" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/33303.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">256</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2</span> New Recombinant Netrin-a Protein of Lucilia Sericata Larvae by Bac to Bac Expression Vector System in Sf9 Insect Cell</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hamzeh%20Alipour">Hamzeh Alipour</a>, <a href="https://publications.waset.org/abstracts/search?q=Masoumeh%20Bagheri"> Masoumeh Bagheri</a>, <a href="https://publications.waset.org/abstracts/search?q=Abbasali%20Raz"> Abbasali Raz</a>, <a href="https://publications.waset.org/abstracts/search?q=Javad%20Dadgar%20Pakdel"> Javad Dadgar Pakdel</a>, <a href="https://publications.waset.org/abstracts/search?q=Kourosh%20Azizi"> Kourosh Azizi</a>, <a href="https://publications.waset.org/abstracts/search?q=Aboozar%20Soltani"> Aboozar Soltani</a>, <a href="https://publications.waset.org/abstracts/search?q=Mohammad%20Djaefar%20Moemenbellah-Fard">Mohammad Djaefar Moemenbellah-Fard</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Background: Maggot debridement therapy is an appropriate, effective, and controlled method using sterilized larvae of Luciliasericata (L.sericata) to treat wounds. Netrin-A is an enzyme in the Laminins family which secreted from salivary gland of L.sericata with a central role in neural regeneration and angiogenesis. This study aimed to production of new recombinant Netrin-A protein of Luciliasericata larvae by baculovirus expression vector system (BEVS) in SF9. Material and methods: In the first step, gene structure was subjected to the in silico studies, which were include determination of Antibacterial activity, Prion formation risk, homology modeling, Molecular docking analysis, and Optimization of recombinant protein. In the second step, the Netrin-A gene was cloned and amplified in pTG19 vector. After digestion with BamH1 and EcoR1 restriction enzymes, it was cloned in pFastBac HTA vector. It was then transformed into DH10Bac competent cells, and the recombinant Bacmid was subsequently transfected into insect Sf9 cells. The expressed recombinant Netrin-A was thus purified in the Ni-NTA agarose. This protein evaluation was done using SDS-PAGE and western blot, respectively. Finally, its concentration was calculated with the Bradford assay method. Results: The Bacmid vector structure with Netrin-A was successfully constructed and then expressed as Netrin-A protein in the Sf9 cell lane. The molecular weight of this protein was 52 kDa with 404 amino acids. In the in silico studies, fortunately, we predicted that recombinant LSNetrin-A have Antibacterial activity and without any prion formation risk.This molecule hasa high binding affinity to the Neogenin and a lower affinity to the DCC-specific receptors. Signal peptide located between amino acids 24 and 25. The concentration of Netrin-A recombinant protein was calculated to be 48.8 μg/ml. it was confirmed that the characterized gene in our previous study codes L. sericata Netrin-A enzyme. Conclusions: Successful generation of the recombinant Netrin-A, a secreted protein in L.sericata salivary glands, and because Luciliasericata larvae are used in larval therapy. Therefore, the findings of the present study could be useful to researchers in future studies on wound healing. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=blowfly" title="blowfly">blowfly</a>, <a href="https://publications.waset.org/abstracts/search?q=BEVS" title=" BEVS"> BEVS</a>, <a href="https://publications.waset.org/abstracts/search?q=gene" title=" gene"> gene</a>, <a href="https://publications.waset.org/abstracts/search?q=immature%20insect" title=" immature insect"> immature insect</a>, <a href="https://publications.waset.org/abstracts/search?q=recombinant%20protein" title=" recombinant protein"> recombinant protein</a>, <a href="https://publications.waset.org/abstracts/search?q=Sf9" title=" Sf9"> Sf9</a> </p> <a href="https://publications.waset.org/abstracts/156898/new-recombinant-netrin-a-protein-of-lucilia-sericata-larvae-by-bac-to-bac-expression-vector-system-in-sf9-insect-cell" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/156898.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">93</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1</span> Chemical and Biological Studies of Kielmeyera coriacea Mart. (Calophyllaceae) Based on Ethnobotanical Survey of Rural Community from Brazil</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Vanessa%20G.%20P.%20Severino">Vanessa G. P. Severino</a>, <a href="https://publications.waset.org/abstracts/search?q=Eliangela%20Cristina%20Candida%20Costa"> Eliangela Cristina Candida Costa</a>, <a href="https://publications.waset.org/abstracts/search?q=Nubia%20Alves%20Mariano%20Teixeira%20Pires%20Gomides"> Nubia Alves Mariano Teixeira Pires Gomides</a>, <a href="https://publications.waset.org/abstracts/search?q=Lucilia%20Kato"> Lucilia Kato</a>, <a href="https://publications.waset.org/abstracts/search?q=Afif%20Felix%20Monteiro"> Afif Felix Monteiro</a>, <a href="https://publications.waset.org/abstracts/search?q=Maria%20Anita%20Lemos%20Vasconcelos%20Ambrosio"> Maria Anita Lemos Vasconcelos Ambrosio</a>, <a href="https://publications.waset.org/abstracts/search?q=Carlos%20Henrique%20Gomes%20Martins"> Carlos Henrique Gomes Martins</a> </p> <p class="card-text"><strong>Abstract:</strong></p> One of the biomes present in Brazil is known as Cerrado, which is a vast tropical savanna ecoregion, particularly in the states of Goiás, Mato Grosso do Sul, Mato Grosso, Tocantins and Minas Gerais. Many species of plants are characterized as endemic and they have therapeutic value for a large part of the population, especially to the rural communities. Given that, the southeastern region of the state of Goiás contains about 21 rural communities, which present a form of organization based on the use of natural resources available. One of these rural communities is named of Coqueiros, where the knowledge about the medicinal plants was very important to this research. Thus, this study focuses on the ethnobotanical survey of this community on the use of Kielmeyera coriacea to treat diseases. From the 37 members interviewed, 76% indicated this species for the treatment of intestinal infection, leukemia, anemia, gastritis, gum pain, toothache, cavity, arthritis, arthrosis, healing, vermifuge, rheumatism, antibiotic, skin problems, mycoses and all kinds of infections. The medicinal properties attributed during the interviews were framed in the body system (disease categories), adapted from ICD 10; thus, 20 indications of use were obtained, among five body systems. Therefore, the root of this species was select to chemical and biological (antioxidant and antimicrobial) studies. From the liquid-liquid extraction of ethanolic extract of root (EER), the hexane (FH), ethyl acetate (FAE), and hydro alcoholic (FHA) fractions were obtained. The chemical profile study of these fractions was performed by LC-MS, identifying major compounds such as δ-tocotrienol, prenylated acylphoroglucinol, 2-hydroxy-1-methoxyxanthone and quercitrin. EER, FH, FAE and FHA were submitted to biological tests. FHA presented the best antioxidant action (EC50 201.53 μg mL-1). EER inhibited the bacterial growth of Streptococcus pyogenes and Pseudomonas aeruginosa, microorganisms associated with rheumatism, at Minimum Inhibitory Concentration (MIC) of 6.25 μg mL-1. In addition, the FH-10 subfraction, obtained from FH fractionation, presented MIC of 1.56 μg mL-1 against S. pneumoniae; EER also inhibited the fungus Candida glabrata (MIC 7.81 μg mL- 1). The FAE-4.7.3 fraction, from the fractionation of FAE, presented MIC of 200 μg mL-1 against Lactobacillus casei, which is one of the causes of caries and oral infections. By the correlation of the chemical and biological data, it is possible to note that the FAE-4.7.3 and FH-10 are constituted 4-hydroxy-2,3-methylenedioxy xanthone, 3-hydroxy-1,2-dimethoxy xanthone, lupeol, prenylated acylphoroglucinol and quercitrin, which could be associated with the biological potential found. Therefore, this study provides an important basis for further investigations regarding the compounds present in the active fractions of K. coriacea, which will permit the establishment of a correlation between ethnobotanical survey and bioactivity. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biological%20activity" title="biological activity">biological activity</a>, <a href="https://publications.waset.org/abstracts/search?q=ethnobotanical%20survey" title=" ethnobotanical survey"> ethnobotanical survey</a>, <a href="https://publications.waset.org/abstracts/search?q=Kielmeyera%20coriacea%20Mart." title=" Kielmeyera coriacea Mart."> Kielmeyera coriacea Mart.</a>, <a href="https://publications.waset.org/abstracts/search?q=LC-MS%20profile" title=" LC-MS profile"> LC-MS profile</a> </p> <a href="https://publications.waset.org/abstracts/96109/chemical-and-biological-studies-of-kielmeyera-coriacea-mart-calophyllaceae-based-on-ethnobotanical-survey-of-rural-community-from-brazil" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/96109.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">141</span> </span> </div> </div> </div> </main> <footer> <div id="infolinks" class="pt-3 pb-2"> <div class="container"> <div style="background-color:#f5f5f5;" class="p-3"> <div class="row"> <div class="col-md-2"> <ul class="list-unstyled"> About <li><a href="https://waset.org/page/support">About Us</a></li> <li><a href="https://waset.org/page/support#legal-information">Legal</a></li> <li><a target="_blank" rel="nofollow" href="https://publications.waset.org/static/files/WASET-16th-foundational-anniversary.pdf">WASET celebrates its 16th 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