From: owner-ammf-digest@smoe.org (alt.music.moxy-fruvous digest) To: ammf-digest@smoe.org Subject: alt.music.moxy-fruvous digest V14 #6846 Reply-To: ammf@fruvous.com Sender: owner-ammf-digest@smoe.org Errors-To: owner-ammf-digest@smoe.org Precedence: bulk alt.music.moxy-fruvous digest Saturday, June 26 2021 Volume 14 : Number 6846 Today's Subjects: ----------------- DroneX Pro - The Drone That Almost Broke The Internet! ["DRONE XPro" Subject: DroneX Pro - The Drone That Almost Broke The Internet! Content-Transfer-Encoding: 8bit ------------------------------ Date: Sat, 26 Jun 2021 07:02:46 -0700 From: "Unusual Secret" Subject: Add this to your water ASAP Add this to your water ASAP http://turntextspeeche.co/hWklaNjI5sNla7Ob3OuOdyAd8bDsHZ3M8JJvpMncN1fQJnVY http://turntextspeeche.co/GPv-eZeqrb1qN7IDhz5WdibvMIlbBoTX6Nz-_iIAG9mFMktd mplete understanding of experimental risks associated with synthetic biology is helping to enforce the knowledge and effectiveness of biosafety. With the potential future creation of man-made unicellular organisms, some are beginning to consider the effect that these organisms will have on biomass already present. Scientists estimate that within the next few decades, organism design will be sophisticated enough to accomplish tasks such as creating biofuels and lowering the levels of harmful substances in the atmosphere. Scientist that favor the development of synthetic biology claim that the use of biosafety mechanisms such as suicide genes and nutrient dependencies will ensure the organisms cannot survive outside of the lab setting in which they were originally created. Organizations like the ETC Group argue that regulations should control the creation of organisms that could potentially harm existing life. They also argue that the development of these organisms will simply shift the consumption of petroleum to the utilization of biomass in order to create energy. These organisms can harm existing life by affecting the prey/predator food chain, reproduction between species, as well as competition against other species (species at risk, or act as an invasive species). Synthetic vaccines are now being produced in the lab. These have caused a lot of excitement in the pharmaceutical industry as they will be cheaper to produce, allow quicker production, as well as enhance the knowledge of virology and immunology. In medicine, healthcare settings and laboratories See also: Biosafety level Biosafety, in medicine and health care settings, specifically refers to proper handling of organs or tissues from biological origin, or genetic therapy products, viruses with respect to the environment, to ensure the safety of health care workers, researchers, lab staff, patients, and the general public. Laboratories are assigned a biosafety level numbered 1 through 4 based on their potential biohazard risk level. The employing authority, through the laboratory director, is responsible for ensuring that there is adequate surveillance of the health of laboratory personnel. The objective of such surveillance is to monitor for occupationally acquired diseases. The World Health Organization attributes human error and poor technique as the primary cause of mishandling of biohazardous materials. Biosafety is also becoming a global concern and requires multilevel resources and international collaboration to monitor, prevent and correct accidents from unintended and malicious release and also to prevent that bioterrorists get their hands-on biologics sample to create biologic weapons of mass destruction. Even people outside of the health sector needs to be involved as in the case of the Ebola outbreak the impact that it had on businesses and travel required that private sectors, international banks together pledged more than $2 billion to combat the epidemic. The bureau of international Security and nonproliferation (ISN) is responsible for managing a broad range of U.S. nonproliferation policies, programs, agreements, and initiatives, and biological weapon is one their concerns Biosafety has its risks and benefits. All stakeholders must try to find a balance between cost-effectiveness of safety measures and use evidence-based safety practices and recommendations, measure the outcomes and consistently reevaluate the potential benefits that biosafety represents for human health. Biosafety level designations are based on a composite of the design features, construction, containment facilities, equipment, practices and operational procedures required for working with agents from the various risk groups. Classification of biohazardous materials is subjective and the risk assessment is determined by the individuals most familiar with the specific characteristics of the organism. There are several factors taken into account when assessing an organism and the classification process. Risk Group 1: (no or low individual and community risk) A microorganism that is unlikely to cause human or animal disease. Risk Group 2 : (moderate individual risk, low community risk) A pathogen that can cause human or animal disease but is unlikely to be a serious hazard to laboratory workers, the community, livestock or the environment. Laboratory exposures may cause serious infection, but effective treatment and preventive measures are available and the risk of spread of infection is limited. Risk Group 3 : (high individual risk, low community risk) A pathogen that usually causes seri ------------------------------ Date: Sat, 26 Jun 2021 13:41:11 +0000 From: "Starbucks" Subject: Leave your feedback and you could WIN! Leave your feedback and you could WIN! http://discounty.us/BZRs8pEs6Ff69CqybuHLJAhVRad5JwV93QF0iOlGTo5G2A http://discounty.us/Qp43Xhjj3hx0iMy9HAdHakrxcot2EIp31jcv5MqM4jgSDA idual to another. Effective treatment and preventive measures are available. Risk Group 4 : (high individual and community risk) A pathogen that usually causes serious human or animal disease and that can be readily transmitted from one individual to another, directly or indirectly. Effective treatment and preventive measures are not usually available. See World Health Organization Biosafety Laboratory Guidelines: World Health Organization Biosafety Laboratory Guildlines Investigations have shown that there are hundreds of unreported biosafety accidents, with laboratories self-policing the handling of biohazardous materials and lack of reporting. Poor record keeping, improper disposal, and mishandling biohazardous materials result in increased risks of biochemical contamination for both the public and environment. Along with the precautions taken during the handling process of biohazardous materials, the World Health Organization recommends: Staff training should always include information on safe methods for highly hazardous procedures that are commonly encountered by all laboratory personnel and which involve: Inhalation risks (i.e. aerosol production) when using loops, streaking agar plates, pipetting, making smears, opening cultures, taking blood/serum samples, centrifuging, etc. Ingestion risks when handling specimens, smears and cultures Risks of percutaneous exposures when using syringes and needles Bites and scratches when handling animals Handling of blood and other potentially hazardous pathological materials Decontamination and disposal of infectious material. Policy and practice in the United States Legal information In June 2009, the Trans-Federal Task Force On Optimizing Biosafety and Biocontainment Oversight recommended the formation of an agency to coordinate high safety risk level labs (3 and 4), and voluntary, non-punitive measures for incident reporting. However, it is unclear as to what changes may or may not have been implemented following their recommendations. United States Code of Federal Regulations The United States Code of Federal Regulations is the codification (law), or collection of laws specific to a specific to a jurisdiction that represent broad areas subject to federal regulation. Title 42 of the Code of Federal Regulations addresses laws concerning Public Health issues including biosafety which can be found under the citation 42 CFR 73 to 42 CFR 73.21 by accessing the US Code of Federal Regulations (CFR) website. International Biohazard Warning Symbol Title 42 Section 73 of the CFR addresses specific aspects of biosafety including Occupational safety and health, transportation of biohazardous materials and safety plans for laboratories using potential biohazards. While biocontainment, as defined in the Biosafety in Microbiological and Biomedical Laboratories and Primary Containment for Biohazards: Selection, Installation and Use of Biosafety Cabinets manuals available at the Centers for Disease Control and Prevention website much of the design, implementation and monitoring of protocols are left up to state and local authorities. The United States CFR states "An individual or entity required to register [as a user of biological agents] must develop and implement a written biosafety plan that is commensurate with the risk of the select agent or toxin" which is followed by 3 recommended sources for laboratory reference. The CDC/NIH publication, "Biosafety in Microbiological and Biomedical Laboratories." The Occupational Safety and Health Administration (OSHA) regulations in 29 CFR parts 1910.1200 and 1910.1450. The "NIH Guidelines for Research Involving Recombinant DNA Molecules," (NIH Guidelines). While clearly the needs of biocontainment and biosafety measures vary across government, academic and private industry laboratories, biological agents pose similar risks independent of their locale. Laws relating to biosafety are not easily accessible and there are few federal regulations that are readily available for a potential trainee to reference outside of the publications recommended in 42 CFR 73.12. Therefore, training is the responsibility of lab employers and is not consistent across various laboratory types thereby increasing the risk of accidental release of biolo ------------------------------ Date: Sat, 26 Jun 2021 05:00:37 -0700 From: "Neck Relax Massage" Subject: The most common techniques used during a neck massage The most common techniques used during a neck massage http://speechgrow.us/MNZd6jk7ckKJflVTl6asYxfea1hnVesFwynMbIC5l7sjrTvQ http://speechgrow.us/UMLh4bkPdyu9YCuM7Hzffzq70j8btKyW_Ho40gj2lsnvYlmJ nual production of more than two million tons of amino acids, mainly L-glutamate and L-lysine. Since some bacteria have the ability to synthesize antibiotics, they are used for medicinal purposes, such as Streptomyces to make aminoglycoside antibiotics. Fermenting tanks with yeast being used to brew beer A variety of biopolymers, such as polysaccharides, polyesters, and polyamides, are produced by microorganisms. Microorganisms are used for the biotechnological production of biopolymers with tailored properties suitable for high-value medical application such as tissue engineering and drug delivery. Microorganisms are for example used for the biosynthesis of xanthan, alginate, cellulose, cyanophycin, poly(gamma-glutamic acid), levan, hyaluronic acid, organic acids, oligosaccharides polysaccharide and polyhydroxyalkanoates. Microorganisms are beneficial for microbial biodegradation or bioremediation of domestic, agricultural and industrial wastes and subsurface pollution in soils, sediments and marine environments. The ability of each microorganism to degrade toxic waste depends on the nature of each contaminant. Since sites typically have multiple pollutant types, the most effective approach to microbial biodegradation is to use a mixture of bacterial and fungal species and strains, each specific to the biodegradation of one or more types of contaminants. Symbiotic microbial communities confer benefits to their human and animal hosts health including aiding digestion, producing beneficial vitamins and amino acids, and suppressing pathogenic microbes. Some benefit may be conferred by eating fermented foods, probiotics (bacteria potentially beneficial to the digestive system) or prebiotics (substances consumed to promote the growth of probiotic microorganisms). The ways the microbiome influences human and animal health, as well as methods to influence the microbiome are active areas of research. Research has suggested that microorganisms could be useful in the treatment of cancer. Various strains of non-pathogenic clostridia can infiltrate and replicate within solid tumors. Clostridial vectors can be safely administered and their potential to deliver therapeutic proteins has been demonstrated in a variety of preclinical models. Some bacteria are used to study fundamental mechanism. An example of model bacteria used to study motility or the production of polysaccharides and development is Myxococcus xanthu ------------------------------ Date: Sat, 26 Jun 2021 06:02:15 -0700 From: "Quickly Improve Alzheimer" Subject: Brain Scan Uncovers Real Cause Of Alzheimer's... Brain Scan Uncovers Real Cause Of Alzheimer's... http://turntextspeeche.co/tAupO9Z5BPZ8LzTjt-MlcSEsqpyan7fp6J3HRvSgt-pSwW_i http://turntextspeeche.co/6n5WC6VGy80T1EfqoEr6ACWOFFsQQzv9QDCGqp5VWEimIV91 safety is the prevention of large-scale loss of biological integrity, focusing both on ecology and human health. These prevention mechanisms include conduction of regular reviews of the biosafety in laboratory settings, as well as strict guidelines to follow. Biosafety is used to protect from harmful incidents. Many laboratories handling biohazards employ an ongoing risk management assessment and enforcement process for biosafety. Failures to follow such protocols can lead to increased risk of exposure to biohazards or pathogens. Human error and poor technique contribute to unnecessary exposure and compromise the best safeguards set into place for protection. Positive-pressure biosafety suit The international Cartagena Protocol on Biosafety deals primarily with the agricultural definition but many advocacy groups seek to expand it to include post-genetic threats: new molecules, artificial life forms, and even robots which may compete directly in the natural food chain. Biosafety in agriculture, chemistry, medicine, exobiology and beyond will likely require the application of the precautionary principle, and a new definition focused on the biological nature of the threatened organism rather than the nature of the threat. When biological warfare or new, currently hypothetical, threats (i.e., robots, new artificial bacteria) are considered, biosafety precautions are generally not sufficient. (link to incident report, i.e. such as problems with CDC research labs in 2014)The new field of biosecurity addresses these complex threats. Biosafety level refers to the stringency of biocontainment precautions deemed necessary by the Centers for Disease Control and Prevention (CDC) for laboratory work with infectious materials. Typically, institutions that experiment with or create potentially harmful biological material will have a committee or board of supervisors that is in charge of the institution's biosafety. They create and monitor the biosafety standards that must be met by labs in order to prevent the accidental release of potentially destructive biological material. (note that in the US, several groups are involved, and efforts are being made to improve processes for government run labs, but there is no unifying regulatory authority for all labs. Biosafety is related to several fields: In ecology (referring to imported life forms from beyond ecoregion borders), In agriculture (reducing the risk of alien viral or transgenic genes, genetic engineer ------------------------------ Date: Sat, 26 Jun 2021 11:48:21 +0000 From: "Psychic Reading" Subject: Need Answers? Ask 1 Psychic Question Need Answers? Ask 1 Psychic Question http://lotterysqri.co/T3sqtRxzZLaXlT7YjZVQfT-l2FOAJjT619RxyXqrzxjY4s8 http://lotterysqri.co/iueTC2QuG5I-TprGCenUXZiRoXcY1axsVkVvrmFwh9zH5Uc ith the launch of the Shojo Beat magazine, Viz Media created new imprints for its manga and fiction lines. The "Shojo Beat" imprint included series featured in the magazine as well as other sh?jo manga titles licensed by Viz after the magazine's conception. Viz began releasing a few Japanese light novels under a "Shojo Beat Fiction" imprint that were related to its "Shojo Beat" manga titles. In February 2006, Viz launched the "Shojo Beat Home Video" line for releasing anime titles primarily designed for female viewers. The first title under the new imprint was Full Moon o Sagashite, the anime adaptation of the same titled manga that was also released by Viz. To promote the new anime line, Viz included a preview disc of the first volume of Full Moon in the June 2006 issue of Shojo Beat. Though the magazine itself has been canceled, Viz stated in May 2009 that it will continue releasing both existing and new series under the "Shojo Beat" manga and anime imprints. Circulation and audience When Shojo Beat launched, it had a circulation of 20,000. In 2006, its average circulation had increased to 35,000, of which 41% were distributed through subscriptions, and the rest sold in newsstands and stores. In 2007, the circulation grew to 38,000, and subscriptions increased to 51%. The magazine's audience was overwhelmingly female, comprising 91% of its readers. Targeted towards "young women", Shojo Beat's "core audience" was between the ages of 13 and 19 and made up 61% of its readers; 47% of readers were 12b17 and 45% were 18b34. Reception Shojo Beat was nominated for a 2008 Society for the Promotion of Japanese Animation Award in the category of "Best Publication", but lost to Japan's Newtype. In reviewing the premiere release of Shojo Beat, IGN's Jessica Chobot sharply criticized the magazine. She felt it looked and read "like a teenie-bopper magazine" and referred to the issue's cover as a "bright, hot-pink, migraine-inducing, bubble-lettered spectacle". She considered the contents boring, and disagreed with Viz's selection of series, noting, "it's as if Viz had taken everything from their backed-up reject pile and tried to pull one over on the female populace. 90% of what I was reading was either poorly drawn or poorly written (more often than not, it was both)." Comic World News' David Welsh disagreed, as he felt that the magazine had several good series, and he praised Nana, Absolute Boyfriend and Crimson Hero as the top three series of the initial issue. Greg McElhatton, co-founder of Wizard: The Guide to Comics and former reviewer for iComics.com, praised the magazine's mainstream appearance, calling it a "smart" decision, as it would draw in its target audience by visually showing them that it's a magazine for teenage girls. While he felt that two of the manga titles in the premiere issue had weak openings, he found that the magazine was "off to a good, if not great start". After its cancellation, Publishers Weekly's Heidi MacDonald reported that the common response she saw from fans was that "everyone liked it but nobody paid for it". She noted that many fans expressed sorrow over the magazine's demise while indicating that they did not subscribe to it. Katherine Dacey, the former senior manga editor for PopCultureShock, remarked that the magazine had offered "just the right mixture of new stories, continuing series, and articles" and praised it for having a "funky, DIY vibe". The staff of the School Library Journal called the magazine "one of a kind" and felt that its loss would leave a void for female fans, a generally under-acknowledged group of comic and manga readers. Staff member Brigid Alverson felt Shojo Beat was a great overall package that "featured intelligent articles that allowed the reader to be enthusiastic about Japanese pop culture without being geeky" making it distinct from other magazines for girls that were normally "filled with brainless celebrity stories or service articles tied to commercial products". Other participants praised the magazine's fashion articles for its educational articles on Japanese culture and for featuring girls of a variety of body types wearing affordable fashions. Two staffers questioned Viz's decision to drop the magazine and wondered if the company had unrealistically expected the magazine to have the same circulation numbers as Shonen Jum ------------------------------ Date: Sat, 26 Jun 2021 06:37:02 -0700 (PDT) From: 20 Subject: =?UTF-8?B?2KfZhNiv2KfYsSDYp9mE2LnYsdio2YrYqSDZhA==?= =?UTF-8?B?2YTYqtmG2YXZitipINin2YTYp9iv2KfYsdmK2Kkg?= =?UTF-8?B?2KjYp9mE2KrYudin2YjZhiDZhdi5INin2YTYpw==?= =?UTF-8?B?2KrYrdin2K8g2KfZhNiv2YjZhNmKINmE2YXYpNiz?= =?UTF-8?B?2LPYp9iqINin2YTYqtmG2YXZitipINin2YTYqA==?= =?UTF-8?B?2LTYsdmK2Kkg2KrYsdit2Kgg2KjYs9mK2KfYr9iq?= =?UTF-8?B?2YPZhSDZiNiq2YLYr9mFINmE2YPZhSDYp9mE2K8=?= =?UTF-8?B?2YjYsdipINin2YTYqtiv2LHZitio2YrYqSDZhdmH?= =?UTF-8?B?2KfYsdin2Kog2KXYudiv2KfYryDZiNmD2KrYpw==?= =?UTF-8?B?2KjYqSDYp9mE2KrZgtin2LHZitixINmI2KfZhNi5?= =?UTF-8?B?2LHZiNi2INin2YTZgdmG2YrYqSBUZWNobmljYWwgUHJvcG9zYWwg2YU=?= =?UTF-8?B?2YYgMSDigJMgNSDZitmI2YTZitmIIDI=?= =?UTF-8?B?MDIxINit2LbZiNixINin2YHYqtix2KfYttmK?= 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http://prayermracle.co/2HKNESfC6Ub3W36OjDVGrkZYu3qGhQzsE4PUV3AGU18_wmo gust 1857, workers began building fences, clearing vegetation, draining the land, and leveling uneven terrain. By the following month, chief engineer Viele reported that the project employed nearly 700 workers. Olmsted employed workers using day labor, hiring men directly without any contracts and paying them by the day. Many of the laborers were Irish immigrants or first-or-second generation Irish Americans, and some Germans and Italians; there were no black or female laborers. The workers were often underpaid, and workers would often take jobs at other construction projects to supplement their income. A pattern of seasonal hiring was established, wherein more workers would be hired and paid at higher rates during the summers. For several months, the park commissioners faced funding issues, and a dedicated workforce and funding stream was not secured until June 1858. The landscaped Upper Reservoir was the only part of the park that the commissioners were not responsible for constructing; instead, the Reservoir would be built by the Croton Aqueduct board. Work on the Reservoir started in April 1858. The first major work in Central Park involved grading the driveways and draining the land in the park's southern section. The Lake in Central Park's southwestern section was the first feature to open to the public, in December 1858, followed by the Ramble in June 1859. The same year, the New York State Legislature authorized the purchase of an additional 65 acres (26 ha) at the northern end of Central Park, from 106th to 110th Streets. The section of Central Park south of 79th Street was mostly completed by 1860. The park commissioners reported in June 1860 that $4 million had been spent on the construction to date. As a result of the sharply rising construction costs, the commissioners eliminated or downsized several features in the Greensward Plan. Based on claims of cost mismanagement, the New York State Senate commissioned the Swiss engineer Julius Kellersberger to write a report on the park. Kellersberger's report, subm ------------------------------ End of alt.music.moxy-fruvous digest V14 #6846 **********************************************