Showing posts with label Research. Show all posts
Showing posts with label Research. Show all posts

Global Lithium Market Industry Forecast

global lithium market industry demand analysis pricing forecast

Majorly used in pharmaceutical drugs to treat bipolar disorder, in lubricants, in the glass industry, and in rechargeable batteries, the lithium market forecast indicates a market growth of 8% CAGR till 2025. 

Further, considering the significant negative impact fossil fuel vehicles have on our environment, the shift toward Electric Vehicles (EV) is growing stronger across the world, marking the rise of many potential industries in South-East Asia, USA, UK, etc. 

Market Industry Demand And Price Forecast 

● According to the US Geological Survey, the global Lithium supply has gone up by 23% in 2019 and is expected to rise continuously until 2025. Amidst the bright promise of tomorrow, the global Lithium production industry welcomed five new players in 2018 (North American Lithium, Tawana Resources, Altura Mining, AMG Advanced Metallurgical Groups, and Pilbara Minerals) in 2018 and outlived the fears of oversupply projected at the beginning of 2024. 

● However, 2019 began on a slightly somber note. The EV vehicle sales have increased by 90% in 2019, but this growth rate is half of the EV vehicle sales growth rate in 2018. This affects the Lithium industry significantly because the EV vehicles industry uses almost half of all the Lithium produced today. 

● During Q2 of 2019, all primary producers and suppliers of Lithium reported a fall in profits and a weaker demand. Nevertheless, all significant producers agree on the market forecast for Lithium, which states that its demand will grow in double digits in the coming quarters. 

● The latest estimates from McKinsey’s Future Mobility Initiative indicate that EV vehicle production will touch the 13 million to 18 million units mark, reaching approximately 26 to 36 million units in 2030. This is a substantial increase compared to the current production capacity of 3.2 million units. This projects an average rise of over five times of today’s demand for Lithium. 

● With Tesla’s Hornsdale Wind Farm Lithium battery for renewable energy solution clearing all suspicions of operational efficiency (with approximately two years of a successful run), more governments are chalking out plans to customize the solution for their requirements. This will also prove a major boost to Lithium demand further in 2025 and the future ahead. 

The major players in the Lithium supply industry are Albemarle, FMC, SQM, Genfeng Lithium Wesfarmers’, Tianqui Lithium, and Global Lithium. 

Risk Analysis 

● Communication and Mobility 

Electronic devices are smaller and stronger than ever: smaller size and extended range of such devices demand a stronger power source such as batteries. To make stronger batteries, industries will need to amp up the technology and amount of raw materials used in the batteries. Lithium is an essential component of such batteries, more so for the rechargeable variants. Hence, the increase in demand for these devices will significantly boost Lithium sales. 

● Energy and Natural Resources 

The rising awareness for Renewable Energy has led to governments placing strict restrictions on fossil fuel-run vehicles, affecting the transportation industry significantly. This is an opening for EV suppliers to fill the demand-supply gap for vehicles. A boost in sales of electric vehicles is a direct push for Lithium demand. 

○ Smart Grid and Energy Storage Solutions: Considering the unsustainability of current solutions for power supply, governments are exploring other options like the Hornsdale Farm Battery. These eco-friendly and economical solutions will see a hike in demand and hence augment Lithium demand. 

○ Inclinations Towards Fewer Chemicals and Simpler Processes: EV industry is consistently looking at solutions to make their car batteries more efficient and economical, to bring down the cost of production of EV products. Technologies like solid-state batteries, Li-S batteries, AL-ion batteries, are some examples of these innovations. This will augment sales for EV vehicles which in turn will raise the Lithium demand. 

● Safety and Health: With research unraveling the secret behind how Lithium aids treatment of bipolar disorder, the acceptance of Lithium in the medical field is bound to increase. This will open another avenue of expansion for Lithium suppliers. 

The Constraints 

● According to a report by KPMG, most of the rechargeable battery based vehicles will be launched in and after 2020. This will put an unavoidable pressure on the Lithium supply market, which may result in a steep rise in Lithium prices as the supply falls short. 

● The EV sales growth in China (the biggest EV consumer) is slowing down, and the fabled EV revolution is not here yet. This is the primary reason why the Lithium industry is facing a slump currently. Considering other factors like government regulation, infrastructure support requirements for electric vehicles, and consumer inertia hampering the rate of sales growth, it is quite possible that the EV revolution gets delayed. The Lithium industry will need to survive this period of a slump. It will be particularly tough for smaller players. 

● While there are unexploited Lithium reserves, for example, the Lithium reserve under Salar de Uyuni salt plains in Bolivia; it might not be possible to sustain the high demand for Lithium as it is already a rare material. 

● Only certain forms of Lithium are suitable for high-performance rechargeable batteries, and the process to obtain, refine, and enrich these forms of Lithium is complex and expensive. Scaling up the current production capabilities to match the high market demand will essentially decide which supplier will stay in the industry. 

Conclusion 

Just like EV vehicles are the new diesel engine, Lithium is the new petroleum. The Lithium industry might suffer a period of the slump for the current year; however, by 2050, the Lithium industry is set to soar and be among one of the most competitive markets. Competitors who can scale up in time and can manage to provide a steady supply of Lithium will be the only ones who survive in the Lithium market of tomorrow. 

Consequently, the rise of the Lithium industry is inevitable. Keep yourself updated on the growing and fluctuating lithium market to insure that your investment is optimized and educated. You can even make a living day trading lithium!

Information About Incidence Rate Market Research

incidence rate market research ir survey study

Are you familiar with the incidence rate in market research? If not, continue reading this article. In market research, the incidence rate (IR) is the factor that has the greatest influence on cost, even more so than the duration of the survey. 

This post will provide you with a better knowledge of the incidence rate in market research by providing specific examples of how a low or high IR might affect the feasibility and expense of your market research project. 

In Terms Of Market Research, What Does Incidence Rate (IR) Stand For? 

The number of people who reply to a survey and end up being eligible for a study is what is meant to be understood as the incidence rate. During market analysis, the term is frequently used interchangeably with the qualifying rate. 

Your incidence rate would be three percent if you had one hundred persons at random who were eager to participate in the survey, but only three of those people truly qualified based on the screening criteria you established. 

An IR of one hundred percent may be generated from a survey of the general population if every single person in the sample pool meets the criteria. Surveys of customers and clients are specifically excluded from the purview of IR for this reason. When you conduct a customer survey by email to each and every one of your clients, those clients automatically qualify for your research. 

Your IR would fall below 100% if you choose to screen as well as qualify only customers who have placed an order with your establishment during the prior three months, though. 

If you are conducting a survey for market research and you are only interested in receiving responses from females, for instance, your incidence rate will suddenly drop from one hundred percent to fifty percent. If you narrow your focus to women who are raising kids younger than 18, you will see an even more significant decline in the incidence rate, which will fall to fewer than 20 percent. 

incidence rate (IR) market research survey study selection

How Do Researchers In Market Research Make Use Of Incidence Rates (IRs)? 

Online panel businesses make use of incidence rates to make estimates regarding how challenging it will be to get in touch with the audience and how many participants would be suitable for the study. 

Assessments with low incidence rates lead to an increase in the amount of effort required to gather answered questionnaires, as well as an increase in the cost of each completed survey and the total cost of the project. This is because it is extremely challenging to gather a high number of completes from an audience that has been hyper-targeted. 

In many instances, if your study anticipates producing an IR of less than 5%, numerous panel firms will see the study as being too risky and will not bid on it. 

A low IR can provide a lot of useful information. It is possible that conducting market research incidence rate won't be possible if the audience you are targeting has an interaction rate of less than 5 percent. Think about relaxing some of your requirements so as to attract a larger number of people, boost the likelihood of success, and cut down on expenses. 

You might anticipate paying extra for a survey that was carried out with a very narrow audience, like decision-makers in B2B transactions. The majority of online panel businesses have B2C pools that are significantly larger than their B2B pools. A large decline in your incidence rate may result from your decision to target particular titles or jobs. 

The following is a list of many methods that may be used to boost IR in market research: 

Improved Targeting 

If you have a field for date of birth in your database file, you may limit the participants in your survey to those who are under the age of 30 by sending invitations to those who were born after a given year. This not only provides a better experience for your consumers by reducing the likelihood of their being disqualified, but it also raises your overall IR for the survey. Find out more by clicking on this page. 

Don’t Be Too Strict With Your Criteria 

Make an effort to relax the stringency of your criteria. If you wish to conduct a survey of customers that visit your business on a weekly basis or more, may this frequency be increased to once every two weeks? Once every thirty days? Because of this, there will be more individuals who are eligible for this. 

Maintain A Flexible Approach To The Quotas 

If you are establishing quotas to guarantee representation from a number of different audiences, you might want to consider relaxing those quotas to make room for oversampling.

How Can ChIP Seq Data Help Biologists In Their Research?

chip seq data researching

ChIP sequencing or ChIP-seq is a high throughput method that combines chromatin immunoprecipitation with next generation sequencing (NGS) techniques. The application of NGS to the chromatin immune-precipitation techniques allows research teams to explore the protein-DNA interactions inside the cell. 

In the case of human beings and other eukaryotic organisms, the chromatin structures and condensation levels vary according to the different stages of the cell cycle. Throughout the life of a cell, different proteins interact and bind to various sites of the chromatin. These play a significant role in the upregulation and downregulation of gene expression. Gene expression is related to disease states and several biological processes. 

The older version of ChIP – ChIP-ChIP used a hybridization array. This technique was thought to have introduced bias into the experiment by using a fixed set of array probes. On the other hand, ChIP-seq technology does not introduce similar biases. It can simultaneously sequence hundreds of precipitated protein-binding sites on the chromatin and find out which sites have proteins bound or unbound during a disease state or cell cycle stage for upregulation or downregulation of gene expression. 

How To Read ChIP Seq Data? 

ChIP-seq is one of the most powerful and accurate techniques for studying DNA-protein interactions or histone modifications across the entire genome. The latest ChIP-seq process generates data that is less complex than the data generated by other forms of parallel sequencing. However, the data set it creates is extensive, and it demands the use of powerful computational methods. that raises the question how to read ChIP seq data? 

Peak calling methods have been standardized over the last decade for the prediction of DNA-binding sites from the ChIP-sequence. One of the simplest and most commonly used methods is MACS – it models the ChIP-seq tag’s shift size and uses the empirical data for enhancing the spatial resolution of the supposed binding sites on the chromatin. 

Although NGS has advanced the sensitivity of ChIP-sequencing, the enormous data produced from the experiment generates new challenges in bioinformatics. Mapping of the resulting data done against a large genome requires pre-indexing structures and considerably large memory. Hence the used software needs to be memory efficient and lightning fast. 

BLAST was the answer to how to read ChIP seq data for almost three decade, but it has its caveats – sequencing errors and SNPs, resulting in mismatches. The new software technology addresses the old challenges in a new way – 

i. By considering gapped vs. ungapped alignment of sequences. 
ii. Solutions for treating non-unique reads. 
iii. Considering the quality value of each nucleotide base in the reads. 
iv. Determining a balance between speed and accuracy of the mapping process. 

While there are several software programs out there that allow reliable mapping and analysis of the ChIP-seq data, there are only a handful few that accommodate a variety of sequencing technologies and interests of application. 

Your team needs software that is not only reliable but also easy-to-use. It should provide replicable results and publication ready formats that holds its respect in the scientific community. 

What Insights Do The Analyses Of ChIP-Seq Data Provide? 

Here are the benefits of analysis of ChIP-seq data – 

Once researchers find the solution to how to read ChIP seq data problems, they will find that assessing the vast library of DNA sites that bind to different proteins of interest to be accurate and replicable. Chromatin immunoprecipitation isolates the regions of the DNA that interact with transcription factors and several other types of protein directly. The technique is used in conjunction with whole-genome sequencing databases to reveal the precise location of the interaction or binding sites. 

The massive volumes of data generated from the NGS of the immunoprecipitated chromatin-protein can be used by biologists to study the role of different proteins in the control of gene expressions during different time frames during cell division. ChIP-seq is applicable to almost all polymerases, transcription machinery, DNA modifications, protein modifications, and structural proteins. 

New Treatment For Breast ER-Dependent Cancer 

Hurtado et al. used ChIP-Seq to find a link between FoxA1 (pioneer factor) and breast cancer treatment. The experiment studied the reduced binding of the estrogen receptor (ER) after a knock-down of FoxA1. It proved that FoxA1 might have a critical role in ER-mediated transcription. It can serve as a therapeutic target in the treatment of estrogen-dependent breast cancer. 

The interactions between the chromatin and transcription factors are potential targets for effective therapeutics with minimum contraindications. The analysis of the data captured from ChIP-seq can contribute to the advances in the field of personalized medicine. 

Evolution Of Transcription Machinery
A research team led by Dominic Shmidt used ChIP-seq for studying the evolution of transcription factors and their binding sites on the chromatin. While a large number of transcription factors are usually conserved among related species, the team decided to focus on CEBPA and HNF4 in the liver tissues. They studied five diverse vertebrate species – humans, dogs, mouse, opossum, and chicken. 

It was one of the pioneering experiments that revealed the evolutionary dynamics that govern the binding of transcription factors to the different regulatory elements of a gene. This chemistry experiment would have been almost impossible with ChIP-ChIP techniques since it used five distinct samples from different species, and the process of designing probes would have been extremely complicated. 

An Insight Into The World Of Protein-DNA Interactions 

Today, further modification of the ChIP-seq techniques have led to the development of different methods of analysis, including the ChIP-seq for protein-RNA interaction in mammalian cells. Other methods include DNase-seq and FAIRE-seq. Both of these methods identify the regulatory regions within the genome. The advancements in the area of analysis and mapping software has answered more or less all questions in the vicinity of how to read ChIP seq data. 

These modifications not only allow the biology research teams to explore the distribution of transcription factors across the entire chromatin, but it also provides replicable information on the epigenetic modifications and biomarkers in the genome that might contribute to the development of specific phenotypes.

The Use Of Chromatography Columns In Scientific Testing

use chromatography columns scientific testing

The Chromatography Column is a lab device that is used for the separation of chemical substances and liquids. The device contains the stationary component and allows the mobile component of the liquid to pass through it conveniently. The device can be effectively used for the separation of both gas and liquids. 

What Are The Types Of Chromatography Columns Used In Laboratories Today? 

There are two types of chromatography columns used in labs today. They are liquid chromatography and gas chromatography. Given below is a brief description of both:

Liquid chromatography column- The liquid chromatography columns that one used to get in the past were made of glass. Today, one will find these columns made of stainless steel, acrylic glass, and borosilicate glass. To stop the stationary liquid from getting out of the device, one uses a net made of ceramic or stainless steel. The size of the net will depend upon the application process. 

Gas Chromatography Column

The gas chromatography column like the liquid chromatography column in the past was made of glass and metal. The latter was often packed with solid stationary particles. Now, changes have been made, and the device has become narrow. They have a coating on silica on the inside of the column that serves the same purpose as the stationary particles that were used in the past. The gas chromatography columns are quite long primarily because they do not have a very high resistance to the flow of the carrier gas. Both the material of which the column is made of as well as the stationary phase of the gas should be compatible with the operating temperatures of the procedure that often might go as high as 300 degrees Celsius and above. 

Buy The Right Chromatography Column From Credible Sources 

One can find both small and narrow chromatography columns to large industrial based ones in the market today. There are credible online websites that helps one find an accurate device for lab projects and testing. These websites are focused on quality materials that are safe and recommended for chromatography lab projects and tests. 

Order Chromatography Column Devices Online 

Thanks to the presence of these credible and esteemed websites, one can effectively order chromatography columns online. The biggest advantage of these online websites is you can effectively order all the products you want from the comforts of any place. The products will be shipped and delivered to your destination without hassles at all. Moreover, when you want to save time and money, make sure you check the online ratings and reviews of these websites before making a purchase. 

Compare Testing Websites

Last but not least, compare websites and choose the best one for your needs. Some websites will also customize the products you want for your needs. Talk to experts and allow them to understand your product specifications so that you can get them on time. With the right websites, you effectively can buy quality products that are safe, certified and perfect for laboratory use and tests! 


I hope you enjoyed this blog post about how scientists can use chromatography columns in scientific testing for research purposes.

Interested in more articles about scientific research and application? 

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VO2 Max Values from the Cycle Ergometer Criterion Test and The Treadmill Criterion test For Merrimack College Undergraduate Student


Abstract

Cycle Ergometer aka Exercise Bike
          This experiment was about finding subjects VO2 max by doing two criterion tests. One was done on a cycle ergometer and the other on a treadmill. Our hypothesis was that the values reached during these exercises would be peak values and not true maximum VO2 values because the subjects would not fully exert themselves due to fatigue and because they were not specifically trained to these modalities. The participants in this lab were four Merrimack College Students between the ages of 20-21 in AH311L in the year 2006. During these tests the subjects heart rate (bpm) and VO2 (ml/kg/min) were monitored, and systolic and diastolic blood pressure (mmHg) were measured during the cycle ergometer test. The VO2, heart rate, and RER (rating of perceived exertion) were found by having the subjects wear a VO2000 gas exchange face mask which was connected to a computer. Graphs were then made based off of these findings and used to see if either subject had reached a VO2 max. For the cycle ergometer criterion test neither of the subjects reached the maximum heart rate that was said to be around 188 bpm. The VO2 max did not plateau and the RER was not >1.1 (Exercise Physiology Laboratory Manual). These are the indicators of VO2 max, and none of them were met. For the treadmill criterion test although two subjects met a heart rate within 12-15bpm of maximum heart rate, the other criteria was not met. The RER’s were not over 1.1 and the VO2 did not plateau. This shows that the treadmill criterion test also did not allow the subjects to reach a VO2 max. After reviewing this data it is safe to say that neither of these tests allowed for all the subjects to reach a VO2 max value because of fatigue therefore can be called peak values.

Introduction
            The determination of maximum oxygen uptake (VO2 max) is a general indicator of cardiorespiratory fitness of an individual (B. Knechtle). VO2 max is the maximal capacity for oxygen consumption by the body during maximal exertion. The more active an individual is will most likely have a higher VO2 max level then a sedentary individual. In a study done with wheel chair athletes, they wanted to test whether an inclinated treadmill or increase in velocity and resistance would produce a valid alternative for getting a VO2 max. Their study shows that the increasing inclination shows an affect on a VO2 max, even though a much better alternative would be to use a hand crank seeing how it would be a more preferred activity (B. Knechtle).
            However, the capacity of prolonged exercise is only partly explained by VO2 max. Thus, another index must be used to assess athletes and healthy persons (C. Schneider). This is true when talking about athletes that train almost year round for a specific sport. If one was to assess that athletes VO2 max on a modality that had a similar affect to the sport that they played, the athlete would not exert themselves, it would take a long time if they did. The athlete should be tested on a different modality or do a different test on the athlete, such as “ventilatory thresholds on blood enzyme activities, antioxidant capacity, or lipid peroxidation” (C. Schneider).
            The purpose of this study was to see if a subject would reach a true VO2 max value on a cycle ergometer with increased resistance or on a treadmill using the Bruce Stage protocol (ACSM 2005). These exercises did not show true maximum values for all of the subjects tested. This can conclude that these tests were not the best in order to prove our hypothesis with the type of subjects that we had.
Methods
          These experiments were designed in order to find subjects VO2 max. The subjects included in this test were four Merrimack College students, two male and two female, that were in the AH311L lab in the year 2006. They were between the ages 20-21 and had already given their informed consent at an earlier date. Also the subjects had filled out a Health history Questionnaire form and a PAR-Q and a liability release. The requirements were explained to the subjects and they were told to wear comfortable athletic clothing and sneakers.

            In the cycle ergometer VO2 max criterion test the subjects had blood pressure, heart rate, and gas exchange monitored throughout the entire test. The subjects were first fitted with a VO2000 gas exchange face mask which was hooked up to a computer. A blood pressure cuff and a heart rate monitor were also fitted to the subjects. The subjects started off with a 2-3 minute warm up with a 0 resistance workload. Then the exercise started by cycling at 50rpm for 3 minutes at a resistance based on the subjects heart rate. The resistance was changed by turning the resistance knob in the positive direction which increased force of friction on the flywheel belt that was being moved by pedaling. After every 3 minutes heart rates, blood pressure, and RPE (rating of perceived exertion) were taken. The VO2 was recorded on the computer because of the gas exchange face mask.  Based on the heart rate numbers the next resistance was then set, which was based off of the YMCA protocol (ACSM, 2005). This data was taken and recorded every 3 minutes until the subject was no longer able to continue.
            For the Treadmill VO2 max criterion test, subjects were tested by using the Bruce 10% protocol (ACSM 2005). The subjects were again fitted with a VO2000 gas exchange face mask which was hooked up to a computer. A heart monitor was used again and obtaining an RPE, but the blood pressure cuff was not used because it is too hard to get a blood pressure while running on a treadmill. The exercise began at a speed of 1.7 mph at a 10% grade. After every 3 minutes heart rate and RPE were taken and the grade was increased by 2%. The VO2 was recorded on the computer because of the gas exchange face mask that was being worn. The subjects continued this exercise until they could no longer continue.
            The data from the subjects were recorded on a sheet and the data acquired from the computer was printed out. For the cycle test, graphs were made for the two subjects in the Tuesday AH311L lab. The graphs consisted of heart rate, VO2, SBP (systolic blood pressure) and DBP (diastolic blood pressure) vs. the Workload. For the treadmill test two graphs were made. One was VO2 vs. Bruce Stage for all four subjects and the second was Heart Rate vs. Bruce Stage for all four subjects. The cycle graphs had best fit lines which told us the R values, but the treadmill graphs did not have these values, it was a line graph.
Results
          The results were obtained from the graphs that were made after all the data was recorded. Figures 1 and 2 represent heart rate, VO2, SBP and DBP vs. Workload for a female and male subject that did the cycle ergometer criterion test. The female subject, figure 1, reached a heart rate of 186 bpm, the RER was 1.10 and the VO2 did not plateau at the end or increase by levels of 2.1 ml/kg/min with an increase in workload. This shows that a VO2 max was not reached even though the heart rate was within 12-15 bpm of subjects possible max heart rate (220-age), the RER was not >1.1 and the VO2 did not reach a plateau. The male subject, Figure 2, reached a heart rate of 181 bpm, RER of 1.07 and the VO2 also did not plateau or increase 2.1 ml/kg/min with an increase of workload. This shows that the male subject also did not reach a VO2 max because the heart rate was not within 12-15 bpm of the subjects max heart rate (220-age), the RER was not >1.1 and the VO2 did not plateau.

In this Criterion YMCA Cycle Ergometer Test 2 Merrimack College undergraduates were tested, 1 male and 1 female, between the ages of 20-21 (mean age 20.5). Subjects were hooked up to a VO2000 gas analysis system (MedGraphics, Inc) with face mask run by its computer program (Breeze Suite 6.1B) as well as an EKG chest strap type heart rate monitor and blood pressure cuff. Resting heart rate was taken from the heart rate monitor and blood pressure was measured manually by another classmate. The YMCA multi-stage cycle ergometer protocol was used (ACSM, 2005). After a 2-3 minute warm-up on the 0 resistance setting heart rates were read off from the heart rate monitor to determine the level of resistance to start at for the workload. Workload was increased by even intervals as resistance was increased every 3 minutes with heart rate and blood pressure taken each interval by a fellow student as well as VO2, and HR being recorded by the computer program. Subjects terminated the test due to leg fatigue and did not reach maximal heart rate levels (220-age). Male subject 177, age 21, achieved a heart rate level of 181 BPM with RPE level of 9 and Female subject 182, age 20, achieved a heart rate level of 186 BPM with RPE of level 9 as well. Plowman would decide that these tests did not achieve maximal levels since HR levels did not reach 188 BPM in both subjects, VO2 Max did not plateau at the end or increase by levels of 2.1 ml/kg/min or less and their RER did not become > 1.1. Therefore they do not satisfy the 3 requirements, so they are peak values and not true maximum values. The fact that subjects terminated the experiment due to leg fatigue and not cardiovascular fatigue confirms that these were not maximum values.

            For the VO2 max treadmill criterion test two graphs were made. Figure 3 is VO2 vs. Bruce Stage for all four subjects that did this test in the year 2006. Figure 4 represents heart rate vs. Bruce Stage for all four subjects. In figure 3 a female subject number 182 had an RER of 1.16 and a VO2 of 25.6 (ml/kg/min) which did not plateau. Female subject number 180 had an RER of 1.14 and a VO2 of 40.4 (ml/kg/min) which did not plateau. Male subject number 177 had an RER of 1.08 and a VO2 of 57.0 (ml/kg/min) which did not plateau. Male subject number 167 had an RER of 1.08 and a VO2 of 63.2 (ml/kg/min) which also did not plateau. Based on this criterion it can be said that none of the subjects obtained a true VO2 max. In Figure 4 the heart rates reached were subject number 180 was 194 bpm, 182 was 184 bpm, 177 was 186 bpm, and number 167 was 177 bpm. The rest was the same as mentioned above for figure 3. Figure 4 was heart rate vs. Bruce Stage; only one subject reached a true max heart rate, subject number 180 with a heart rate of 194 bpm. The rest of the data also shows that this subject reached an RER of 1.14 which is >1.1, but the VO2 did not plateau so the data did not meet all 3 of the criteria.
Four Merrimack College students, two male and two female, ages 20-21 (mean 20.5) performed a Criterion Treadmill Test using Bruce 10% protocol (ACSM 2005) while wearing a VO2000 gas exchange face- mask.  During the experiment, the subjects’ heart rate and V02 were recorded by a computer, connected to the gas exchange mask.  The Subjects were asked to walk/run on a treadmill for 4 different stages of inclination and speed.  Each stage lasted for 3 minutes and the work increased from stage 1 to stage 4.  The subjects were asked to perform the exercise until they could not perform any more.  Figure 1 shows the relationship between Stage of work done on the treadmill and the subjects V02.  It is concluded that none of the subjects actually reached a V02 max by using the 3 criteria for maximal exertion. The Criteria is having a heart rate 12-15 BPM from maximum heart rate, a VO2 plateau, and having an RER > 1.1. Although the subjects did not reach a V02 max, Figure 1 illustrates a positive relationship between Stage and V02.

Four Merrimack College students, two male and two female, ages 20-21 (mean 20.5) performed a Criterion Treadmill Test using Bruce 10% protocol (ACSM 2005) while wearing a VO2000 gas exchange face- mask.  During the experiment, the subject’s heart rate and V02 were recorded by a computer connected to the gas exchange mask.  The Subjects were asked to walk/run on a treadmill for 4 different stages of inclination and speed.  Each stage lasted for 3 minutes and the work increased from stage 1 to stage 4.  The subjects were asked to perform the exercise until they could not perform any more.  Figure 2 shows the relationship between stage of work done on the treadmill and the subject’s heart rate.  It is concluded that only one the subjects actually reached a max exertion by using the 3 criteria for maximal V02 exertion. The Criteria is having a heart rate 12-15 BPM from maximum heart rate, a VO2 plateau, and having an RER > 1.1. Although the subjects did not reach a max heart rate, Figure 2 illustrates a positive relationship between Grade and heart rate.


Discussion

          The hypothesis that that the values reached during these exercises would be peak values and not true maximum VO2 values because the subjects would not fully exert themselves due to fatigue and because they were not specifically trained to these modalities seems to be supported by the results of this experiment. The correct determination of VO2 max requires a maximum degree of exertion (B. Knechtle).
 Only one subject seems to have the right criteria to have a true VO2 max. The other subjects did not reach a maximum heart rate, an RER >1.1 or have their VO2 plateau. Since the criterion was not met, it can be said that the other subjects only had peak VO2 values and not true VO2 max values. The results obtained support our hypothesis.
            The Cycle ergometer criterion VO2 max test and the Treadmill criterion VO2 max test were different in the way that they affected each subject. The cycle ergometer test could have some possibilities of error based on the equipment and the subjects. The VO2000 gas exchange face mask caused some problems during the exercise. The mask was larger then the subjects faces which caused it to not fit correctly. This in turn might not have given the best results for VO2 because the mask might have been letting air out the sides of the mask, not giving a good reading on the gas exchange. Also the heart rate monitors might not have been placed in the right spot on the subjects or have fallen down, giving an inaccurate reading. Subjects discontinued the test because of leg fatigue and because none of them were trained on this modality.
            The treadmill criterion VO2 max test also has some possibilities of error based on the equipment and the subjects. The VO2000 gas exchange face mask was used in this test also and it similar problems with it. The masks were too big for the subjects and caused it to give an inaccurate reading by allowing the air to leak out the sides of the mask. The heart rate monitors also could have been a problem because the impact of running, causing the monitor to slip down and give an inaccurate reading. The subjects also stopped both exercises on account of leg fatigue, so neither of the tests was carried out for the entire length.

            These tests were a better indication of whether or not a true VO2 max was met then the Pacer, Questionnaire, and YMCA cycle tests. This can be said because the Pacer test had many sources of error such as not doing the exercise right and heart rate monitor malfunctions. The Questionnaire was based on what the subject had to say about their exercising, many could have lied and calculated a VO2 max that was not true. In the YMCA test it was not an all out effort; some subjects also became too fatigued to reach a VO2 that was close to a maximum value. These tests did not give us accurate VO2 results and the criterion tests gave better and closer values to a VO2 max.
            Some ways to possibly improve these tests would be to find masks that would better fit the subjects’ faces in order to give better results. As for the heart rate monitors, there should be a better way to get this since it kept slipping off of the subjects. The exercises also caused the subjects to end the tests early due to fatigue and increase of velocity or inclination. If the exercises weren’t as intense or if the subjects were better trained results might have been more accurate. If the exercise protocol were performed for the fixed time rather than to exhaustion, the protective effects of training would have been observed (C. Schneider).


Works Cited

Biology/ AH Dept. 2006 Exercise Physiology Laboratory Manual Fall, 2006 Merrimack College, Pgs 6.1-7.3

Davis, Shala E. Dwyer Gregory B. 2005 ACSM Health Related Physical Fitness Assessment Manual, Lippincot Williams & Wilkins, Baltimore. Pg 104, 119

B. Knechtle W. Kopfli, 2001. Treadmill Exercise Testing with Increasing Inclination as Exercise Protocol for Wheelchair Athletes, International Medical Society of Paraplegia, pg 633

Claudia Schneider Jaqueline Barp, 2005, Oxidative Stress After Three Different Intensities of Running, Canadian Society for Exercise Physiology, pg 723-734


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Research Paper: Emancipation of the Addicted



Smoke billows through the dimly lit basement. The room is silent, except for the low muffled breath of a man slouched upon a tattered sofa. As the smoke begins to rise and dissipate into the darkness of the room, the man sinks lower and lower into the sofa. Although the basement appears cold and dark, much like a prison cell, the true shackles upon this man is his addiction to methamphetamines. His once successful and satisfying life is a mere memory, his happiness disappearing much like the smoke into the air.  For an addict breaking the cycle of using is almost impossible, especially with a drug of this caliber. With each dose of the lethal substance, the addict becomes less likely to break his habits and therefore hurtles himself towards a life of despair and ultimately death. But what if this man’s life could be saved?
            Throughout our lives we will meet someone who has struggled and lost the battle with addiction. We feel powerless and hopeless because our efforts can not prevail over the strangle hold drugs take on the body and mind. However, through the efforts of researchers in the neurolobiological, saving these people’s lives no longer is wishful thinking, but rather a promising possibility. Mankind has been plagued with addiction for as long as time has existed, but with the new drugs that permeate our world the urgency for a cure for addiction is never more present. If a neurological cure cannot be found for addiction, more powerful and addictive drugs have the potential to plague mankind. A cure is needed for our future. Perhaps there is one closer than we think?
            A recent study conducted by Dr. Rita Z. Goldstein in the Trends in Cognitive Sciences Journal implies that the futility of addiction may simply be a thought of the past. The key word in this is thought; the study asserts that addiction can possibly be cured by a combination of awareness about the severity of one’s addiction as well as a neurologically based treatment. Through a series of studies it is determined that addiction undermines a person’s ability to recognize their addiction as a problem because the addiction itself causes neural circuits to act in a dysfunctional way. Therefore, an addict is simply not in denial, but their neurological make up is distorted causing them to be unaware of their social, emotional, and cognitive state. This state of unawareness is analogous to the effects that a psychological disease, such as schizophrenia, takes on the mind. Similarly in addiction, the affected party experiences a disconnect between what they believe is happening and what is actually happening.
            In an examination of emotional responses between a group of heavy cocaine users and non-users this incongruity of reality was revealed. Certain images were presented to each subject, ranging from pleasant, neutral, unpleasant, and cocaine, that showed in each instance the groups differed greatly in their response. This is due to the power that cocaine takes on perception, which is controlled through our neurobiological make up. The study suggests that the skewed results in these responses is due to the adverse effects that drugs have on our body’s homeostasis. The physiological condition of our body influences our perception, and therefore can change how we interpret signals from our body.
            From a neurological standpoint the study examined how the anterior insula and cingulate influence our perceptions of reality. An integral part of the study revealed that damage to the anterior cingulate causes errors in awareness, which motivate the behavior of drug use. In contrast however, a recent study reveals that damage to the anterior insula actually benefits the drug users because it is extremely important in the rewards system of the brain. For example, damage in insula activity in rats with prolonged addiction to amphetamines allowed them to quit their addiction with few problems. In similar studies, a lesion in the right insula revealed that smokers were infinitely less likely to have relapses in comparison to smokers who were not given this lesion. These findings in rats however are revolutionary because it was once believed that damage in insula activity could only be attributed to the relief of addiction in smokers. Now, these findings have profound implications for the liberation of addiction in other drugs. The culmination of this research asserts that the awareness and control of addiction can be dramatically influenced by the proper workings of the anterior cingulate and the careful manipulation of the insula activity.
            In the near future, this research will have real world implications that could possibly save the lives of countless people facing addiction. In conjunction, intensive cognitive training that stresses self-awareness and pharmacological practices could end addiction forever. In the study on amphetamine addicted rats an injection of lidocaine quelled their addiction to this deadly drug by inhibiting the functionality of insula activity. Although additional studies are needed, neurobiologists will be able to refine and apply their knowledge of how insula activities control addiction and perhaps find a permanent cure.
            Although the article appeared extremely complex and foreboding, the underlying message about addiction and the possibility of a cure was easy to grasp. After completing the research and understanding the article, the ideas presented within it are amazing. The real world implications of this are not only astounding, but tangible. Whether a person is addicted to a drug or the ramifications of the actions of an addict influence them, everyone is impacted by addiction in some way. The possibility of a long-term and effective cure for this is simply amazing. The study leaves a window of research and application of drug addiction open, but I am confident that through this window there is a cure.

Works Cited
Goldstein , Rita. "The Neurocircuitry of Impaired Insight in Drug Addiction." Trends in Cognitive Sciences (2009): 1-14. Web. 13 Sep 2009.
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Research Paper: HIV - There Is Hope



HIV – There is Hope
           
            In the sub-Saharan region of Africa mankind is plagued by the HIV virus. Governments, schools, and other essential parts of society cannot function because of the catastrophic implications of HIV (and AIDS). In turn, in these affected regions society as a whole cannot progress. Although there are effective methods to treat the symptoms of HIV and restore the majority the immune system’s vitality, the region aforementioned cannot afford these expensive treatments. Thus, until there is an effective vaccine to prevent the HIV virus, sub-Saharan Africa will not escape its state of destitution.
Millions of people die each year after HIV reaches Stage 4 and progresses into AIDs. With an increasing number of infected people the need for a cure is never more present. Countless attempts have been made to quell the virus, yet each has failed to find an answer. However, an experimental vaccine study revealed that there may be hope for HIV patients looming on the horizon. By no means is this experimental vaccine the solution to the “plague” upon humanity, but rather proof that through extensive research and experimentation there could be a preventive vaccine for HIV in the near future.
The research exhibited in Thailand regarding the experimental vaccine for the HIV-1 infection described Dr. Berkhout in the Retriovology journal proposes monumental results. For the RV144 Phase III clinical trial, the patients that received the experimental vaccination, as opposed to the placebo vaccination, demonstrated an increased resistance to the HIV-1 virus of 31%. Although the resulting percentage of protective efficacy was lower than the value for a vaccination to be considered “unequivocal clinical benefit,” the shear fact that the vaccination showed signs of improving defense against the HIV-1 virus is promising.
The vaccine discussed above is composed of two elements. The first component of the vaccine, ALVAC, is used in priming and consists of a synthetic version of three HIV-1 genes that encode proteins of the Envelope of the virus. ALVAC is a viral vector based vaccine whose purpose is to promote human immune cells to recognize and fight against the HIV-1 virus. In conjunction with ALVAC, AIDSVAX is used to fight the HIV-1 virus. AIDSVAX utilizes boosting antigens that are engineered to mimic the Envelope proteins in the virus, which allows the body to recognize the virus before one is infected. Thus, AIDSVAX stimulates the production of antibodies that are needed in fighting the HIV-1 virus. In the study, each participant was given four shots of ALVAC and two shots of AIDSVAX. Typically, vaccines that protect against virus infection also have an impact on the amount of the virus in the individuals that it did not protect from infection. However, the study discovered an anomaly in the vaccine by concluding that while the combination of the two vaccines had a moderate effect on viral protection, it simultaneously had no effect on the total virus load of an infected patient.
            Although the study appears to reveal the possibility of a future without HIV and AIDS, there are still many questions and skepticism regarding the results of the experiment. The most compelling argument against the validity of the vaccine is the fact that it addresses the subtypes of the virus A and C, neither of which are predominate in the sub-Saharan region. The dominant subtypes of HIV-1 in this region are B and E. However, this argument does not carry much ardor because it is relatively easy to modify the vaccine to target the subtypes of HIV-1 in the sub-Saharan region. Another study must be conducted because the RV144 study only contained minimal cases of participants with the HIV-1 infection. Thus, the statistical data could be skewed by a relatively minute amount of people who put themselves at risk by practicing “high-risk” activities.
            The underlying message of the experiment reveals that there is extensive work still left to be done in order to achieve the ultimate goal of finding an effective HIV-1 vaccine. The most important work left to be done is identifying the mechanism or molecule that causes the correlation with the protection from the virus. If discovered, this mechanism or molecule can be manipulated in order to make a more effective and widespread HIV vaccination. The possibility of eradicating HIV to any extent is extremely important because of the social, economic, and political implications.
            The article was written in a very concise and easy manner to understand. However, the doubt in the author’s voice was extremely evident in the constant assertion that these results not only need to be tested again, but also that the validity of the experiment needs to be increased. The provisional vaccine appears to be promising, yet there is much work left to be done. This experiment was initiated in 2003 and it lasted for six years, which indicates that the possible solution to HIV-1 will take many years. However, the findings appear to be so promising that I am confident that soon, the plight of HIV-1 will be eradicated.
Works Cited
Berkhout, Ben. "HIV vaccine: it may take two to tango, but no party time yet." Retrovirology 6. (2009): n. pag. Web. 21 Oct 2009.

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Research Paper: Gene Malfunction in Autism



Gene Malfunction in Autism

            The genome is the most complicated and intricate entity ever discovered. Billions of building blocks come to together in perfect harmony to encode for life. The complexity and extreme specificity of coding produced in the DNA of every living organism, and within every living cell, is comprised of only four nucleotides. It is amazing to ponder the idea that all of life can be explained by the assortment and rearrangement of just four simple building blocks, Adenine, Thymine, Guanine, and Cytosine. In a healthy and stereotypical organism, the organization of these nucleotides is carried out flawlessly in almost every cell throughout the body, each containing the same set of perfectly ordered pairs. Although the human genome is nearly perfect in its attempt to copy and organize its DNA to allow man to thrive, a small minority of people are unfortunate enough to endure the wrath of this near perfection.
            So what happens when the human genome endures a problem in its coding of nucleotides? Often, a mistake in the DNA coding goes unnoticed, meaning the mutation in the ordering of nucleotides does not affect the organism as a whole. However, when the mutation is significant, dramatic changes in the organism are evident, and often devastating. There are countless diseases that are caused by a simple miscoding among nucleotides, which impair the person and negatively affect their development and ability to function. In order to better understand and perhaps find a cure for these genetic based diseases, science must first grasp and interpret the malfunction occurring on the DNA level. Although these diseases have permeated mankind for thousands of years, the strides in genomic based science has allowed an imperceptible growth of understanding. These diseases, such as autism, are an urgency that must be better understood in order for man to escape the tragic and devastating blight that they inflict.
            In a recent study conducted by Dr. Simon Gregory published in the BioMed Central Journal, the mystery of the genetic causes of autism were discussed. The experiment and subsequent analysis of possible genetic malfunctions related to autism proposes a correlation between a deficiency in the oxytocin receptor in the human body. The method in which the experiment was conducted was that a high-resolution genome-wide microarray and comparative genomic hybridization identified variants within 119 probands from families with multiple cases of autism. Next, the experiment continued by undertaking DNA mythylation analysis of peripheral blood and temporal cortex DNA of autism cases and compared that with a control group. One aspect in identifying the mechanism that causes autism is the genes that characterize copy number variants, or CVNs. The most important and significant aspect of the experiment discussed is that the deletion of the oxytocin receptor gene, OXTR. These findings were further explored by observing the correlation between OXTR and autism by using epigenetic analysis of the promoter region of this. Although autism is a complex and intricate disease, just like any genetic disorder, the misregulation of OXTR is the main focus of the experiment in an attempt to explain the disorder.
            In the experiment it was determined that the CVNs were extremely significant in a correlation with autism in patients. In the 119 autism probands a total of 113 within 111 autistic individuals exhibited one or more deletions or duplications, ranging from one to six CNVs per individual. Previously, only one of the genes in question were associated with autism, yet the experiment reveals that there are far more than that. Now not only is a deletion on the chromosome 8q22.2 associated with this disorder, but also deletion of sections within the chromosomes 2q24.1-2q24.3, 15q11-13, and 3p25.
            Similarly, the deletion of OXTR could result in a reduction in levels of OXTR available during the development of a child in utero, which may lead to the development of autism. Although this is a possibility, it does not account for the fact that one child in a family with this deletion of OXTR may have autism, but a child in the same family with the same deletion does not have autism. Thus, this study reveals that there must be another mechanism that has a profound influence on autism. In conjunction with this idea, it is determined that the increase in DNA methylation leads to gene silencing, which can be a factor in autism. An increase in DNA methylation of found within a critical region of OXTR regulation may be a more important factor and could represent a more generalized reason for autism. For example, in the study a group of autistic males with an increase in methylation in the .934 site exhibited 20% less expression. Thus, OXTR has a significant correlation with decreased expression of the gene associated with autism.
            The article was significantly more difficult to read than any other article thus far. It was difficult to infer the meaning of the information because most of the terms were not familiar, and the context clues surrounding them were just as or more difficult. However, the ideas behind the words were relatively easy to understand. The implications of understanding the mechanisms behind a serious disease like autism has profound real world applications. Although this is just one of many studies that must be done to understand the reason for autism on a genetic level, it is a small preview of what is to come. It may seem like an impossibility for autism to be cured, but once it is fully understood and personalized genomes are economically sensible, it is a distinct possibility that autism, and related diseases, may be a worry of the past. This is an urgency of the twenty-first century, yet with sufficient research and experimentation science will discover a solution.


Works Cited
Gregory, Simon. "Genomic and epigenetic evidence for oxytocin receptor deficiency in autism." BioMed Journal (2009): n. pag. Web. 15 Nov 2009.

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