Human Impacts On The Rainforest-Past And Present

Directions: For each time frame below, provide the amount of trees per acre and rate of destruction (or improvement if that is the case). Fill in the remaining portions of the chart. Be sure to include at least three academic sources (please do not use blogs or Wikipedia). For maximum points, include detailed information, include units, and include citations.

 

Rainforest 20 Years Ago 10 Years Ago Present Condition Reasons for decline (ex: agriculture, logging, mining, ranching, urbanization, etc.) Animals affected by deforestation and current plans to improve numbers
Amazon Rainforest

 

 

         
Australian Rainforest

 

 

 

 

 

 

         
Congo Rainforest

 

 

 

 

 

 

 

         

 

Now that you are aware of the issues, what are some things you can do as a consumer to help preserve the rainforest? Provide at least two examples and use complete sentences.

 

What are two ways you can help raise awareness for a species that has become endangered due to deforestation? Use complete sentences.

Refere

 
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DNA and Genes Lab Activity

DNA and Genes Lab Activity

 

Complete your answers in the spaces provided. USE YOUR OWN WORDS – Yes even for definitions! Remember to add your last name and first initial to the file name prior to saving and submitting your completed assignment through Canvas.

 

 

 

Use your textbook, notes and these websites to answer the pre lab questions. http://learn.genetics.utah.edu/units/basics/transcribe/ http://www.vcbio.science.ru.nl/en/virtuallessons/cellcycle/trans/

 

 

 

Pre Lab Questions:

 

1. What is the product of transcription?

 

 

 

2. What is the region of DNA called where transcription begins?

 

 

 

 

3. What is the product of translation?

 

 

 

 

4. In your own words define each of the following: Silent mutation

 

Missense mutation Nonsense mutation Frame shift mutation

 

 

 

5. Where in the cell does translation take place?

Click on the link below to access the online lab.

 

http://www.mhhe.com/biosci/genbio/virtual_labs_2K8/pages/DNA_And_Genes.html

 

Download and print the instructions for reference as you work through the lab. As you work through the lab fill in the table below. Use this information to answer the questions that follow contained in this document.

 

First read through the mutation guide. Once you close the guide you will see the buttons to begin the simulation. Note, you will be translating the mRNA strand into a protein.

As you work through each of the mutations fill in the charts below. You must complete 4 mutations for this lab activity. It’s good practice working with the codon table .

 

– Aris labs calls the codon table the ‘Genetic Code Chart’. Use the amino acid abbreviation for the protein sequence. For example the amino acid proline is abbreviated as pro.

 

You have to fill in all the letters AND the resulting amino acid sequence by dragging and dropping before you click the [check] button. Abrieviate STOP as either STP or END.

 

For each of the three mutations you will complete, fill in the table in this lab document with the original mRNA and amino acid sequence and the mRNA sequence and the resulting amino acid sequence RESULTING FROM the mutation as outlined in the mutation rule.

 

The various mutations represent missense, nonsense, silent and frame shift mutations. You must complete one of each. The lab will not necessarily present the mutations in this order. You must do the mutation and identify which type it is and make sure you do one of each.

 

 

 

6. Frame Shift Mutation example:

Provide the mutation rule you are following.

 

 

 

 

 

 

Original

A. Acids

                 
Original

mRNA

                 
Mutated

mRNA

                 
Mutated

A. Acids

                 

 

 

7. Missense Mutation example:

Provide the mutation rule you are following.

 

 

 

 

 

 

 

Original

A. Acids

                 
Original

mRNA

                 
Mutated

mRNA

                 
Mutated

A. Acids

                 

 

 

 

 

8. Nonsense Mutation example:

Provide the mutation rule you are following.

 

 

 

 

 

 

Original

A. Acids

                 
Original

mRNA

                 
Mutated

mRNA

                 
Mutated

A. Acids

                 

 

 

9. Silent Mutation example:

Provide the mutation rule you are following.

 

 

 

 

 

 

Original

A. Acids

                 
Original

mRNA

                 
Mutated

mRNA

                 
Mutated

A. Acids

                 

 

 

 

Post Lab Questions

 

10. From the mutations you have explored, which one is the least severe. Explain your answer.

 

 

 

 

 

 

 

 

 

 

 

11. From the mutations you have explored, which one is the most severe. Why?

 

 

 

 

 

 

 

 

 

 

12. Aside from silent mutations which have no effect on amino acid sequence, are all mutations bad? Explain your answer.

 

 

Lab 10 Classification of Organisms

 

Complete your answers in the spaces provided. USE YOUR OWN WORDS – Yes even for definitions! Remember to add your last name and first initial to the file name prior to saving and submitting your completed assignment through Canvas.

 

The lab website has post lab questions – these are not necessary – you only have to complete the questions in this lab assignment document.

 

http://www.windows2universe.org/earth/Life/classification_intro.html http://www.ric.edu/faculty/ptiskus/six_kingdoms/index.htm http://anthro.palomar.edu/animal/default.htm

 

 

 

 

 

Pre Lab Questions

 

1. What are the three domains of life? Provide the domain name and basic characteristics for each.

 

 

 

 

 

 

 

 

 

 

 

2. List the 4 Kingdoms of the Eukaryotic Domain and their basic characteristics.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

3. What is the difference between a heterotroph and an autotroph?

 

 

 

 

 

 

 

Use the link below to go to the lab site:

http://www.glencoe.com/sites/common_assets/science/virtual_labs/E07/E07.html

 

In the upper right there is a box with five organisms. Drag each one individually to the magnifying glass to learn more about it. After reading about its characteristics drag it to the appropriate kingdom box in the middle of the screen. Do this for all the organisms in the box and click the check button. Click reset to work your way through the ten organisms in the table below.

 

4. Table 1

Organism Name Kingdom Key Feature(s) for Classification
 

Tapeworm

   
Plumose Anemone    
Euglena gracilis    
Wisk fern    
Archaeoglobus    
Sargosso weed    
Paramecium    
Methanosarcina

barkeri

   
Living stone    
Methanopyrus    

 

Kingdoms are further divided into phyla. Table 2 below lists parameters for 8 of the Animal Kingdom Phyla: Porifera, Cnidaria, Platyhelminths (flatworms), Nematodes (roundworms), Molusks, Annelids, Arthropods, and Chordates. Here’s some websites to visit for additional information:

 

http://waynesword.palomar.edu/trnov01.htm http://www.uic.edu/classes/bios/bios100/labs/animaldiversity.htm

Animal Kingdom

 

Animalia Phylum Symmetry Other Characteristics Examples
 

 

 

 

 

 

 

 

Sea Life

 

 

 

Porifera

 

 

 

None

– No nervous, digestive, or

circulatory systems

– Filter feeders

Sponges
   

 

 

Cnidaria

 

 

 

Radial

– True tissue differentiation

and nematocyts

Jellyfish, Coral,

Hydra

   

Mollusca

 

Bilateral

– True coelom

– Soft body; some secrete calcium based shell

Squid,

Cuttlefish, Octopus, Snail

 

 

 

 

 

 

 

 

 

 

Worms

 

 

 

Platyhelmi nth

 

 

 

Bilateral

– Unsegmented

– Nervous system and true organs

– Single opening to digestive tract

Flatworm,

Tapeworm

   

 

 

Nematode

 

 

 

Bilateral

– Unsegmented

– Nervous and digestive system

Roundworm
   

 

 

Annelid

 

 

 

Bilateral

– Segmentation

– Nervous, digestive, and circulatory systems

Earthworm,

Leech

 

 

 

Invertebrates

 

 

 

Arthropod

 

 

 

Bilateral

– Segmentation

– Exoskeleton

– Circulatory system

Spider, crab,

scorpion,

lobster, crayfish, shrimp, insects

 

 

 

Vertebrates

 

 

 

Chordate

 

 

 

Bilateral

– Endoskeleton

– Nervous, digestive, and circulatory systems

Mammal, Bird,

Reptile, Amphibian, Fish

 

 

 

 

 

 

 

Fill in the Table 3. Provide the definition in your own words and an example organism and phyla. You can choose example organisms from the lab you’ve completed, the phyla characteristics table above, or one you come up with on your own.

 

Table 3

 

Characteristic Definition Example Organism Phyla of Example

Organism

Endoskeleton      
Exoskeleton      
Radial

symmetry

     
Bilateral

symmetry

     
True Coelom      
Segmentation

(Body)

     

 

 

 

Hardy Weinberg Homework

The following websites have alternative ways of explaining the Hardy Weinberg Principles. http://nortonbooks.com/college/biology/animations/ch17p01.htm

http://www.k-state.edu/parasitology/biology198/hardwein.html

https:/ /www.youtube.com/watch ?v=xPkOAnK20kw http://integrativebiology.okstate.edu/zoo_lrc/biol1114/tutorials/Flash/life4e_15-6-OSU.swf

 

 

 

The Hardy Weinberg Principle states that allele frequencies do not change over time if 5 parameters are met. There can be no natural selection, no migration into or out from the population, no mutation, all mating must be random, and the population must be very large. In this lab you are going to use a small population to simulate the effect these parameters can have on allele frequencies.

 

First you must remember that each individual possesses two alleles of each trait. So an individual who is homozygous for color (B = Black, b = brown) BB has two copies of the B allele. A heterozygous individual has one B allele and one b allele. Finally a homozygous recessive brown individual has two copies of the b allele.

 

For example in a population of 100 flies you gathered the following information: 20

Homozygous Black, 40 Heterozygous Black, 40 Homozygous Brown. The allele numbers for this population are shown in the table below.

 

Genotype Number in

Population

Total # B

alleles

Total # b

alleles

BB 20 40 0
Bb 40 40 40
bb 40 0 80
totals 100 80 120

 

 

There is a difference between the actual alleles and an estimate of the alleles for a population. If you know the genotypes of all the individuals you can calculate the actual allele frequencies by dividing the total number of one allele and dividing it by the total number of all alleles for that population. In our example above the actual frequency of the B allele is calculated by dividing

80 (the total number of B alleles for the population) by 200 (the total of all the alleles of the population. 80/200 = 0.4. Therefore P = 0.4 You can then use the formula P + q = 1 to determine the frequency of q. 0.4 + q = 1 so q = 0.6.

1. In a population of 100 flies you gathered the following information: 15 Homozygous Black, 30 Heterozygous Black, 55 Homozygous Brown. Using this information fill in the chart below and answer the questions

 

Genotype Number in

Population

Total # B

alleles

Total # b

alleles

BB      
Bb      
bb      
totals      

 

 

 

 

2. What percentage of the population is phenotypically Black? Explain your answer.

 

 

 

 

 

 

 

3. Calculate the actual allele frequency of B. Provide a full explanation of your work .

 

 

 

 

 

 

 

 

 

 

 

 

 

 

4. Explain the concept of non-random mating.

5. Does non random mating increase or decrease the genetic diversity of a population. Explain your answer.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

6. List the Hardy Weinberg principles.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

7. What happens to the allele frequencies of a population if all Hardy Weinberg principles are met?

 

 

 

 

 

 

 

 

8. Which genotype (homozygous dominant, heterozygous, homozygous recessive) is known just by their phenotype? Why?

 

 

 

Lab 11 Population Biology

 

Complete your answers in the spaces provided. USE YOUR OWN WORDS – Yes even for definitions! Remember to add your last name and first initial to the file name prior to saving and submitting your completed assignment through Canvas.

 

The lab website has post lab questions – these are not necessary – you only have to complete the questions in this lab assignment document.

 

Use your textbook, notes and these websites to answer the pre lab questions. http://www.marietta.edu/~biol/biomes/ecology.htm http://marinebio.org/Oceans/Conservation/Moyle/ch7.asp

 

 

 

Pre Lab Questions

 

1. Define habitat.

 

 

 

 

2. Define niche.

 

 

 

 

 

 

3. Define carrying capacity.

 

 

 

 

 

 

4. How many species can occupy a niche? Why is this the limit?

 

 

 

 

 

 

 

Go to the following site: http://www.mhhe.com/biosci/genbio/virtual_labs_2K8/pages/PopulationBiology.html Download and print the instructions so you can work through the lab. As you work through the lab fill in the table below. Use this information to answer the questions that follow contained in this document.

5. Explain the difference between interspecies and intraspecies competition. Provide an example of each: interspecies and intraspecies competition.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

6. List the reasons a population reaches its carrying capacity.

 

 

 

 

 

 

 

7. Fill in the table below with your data from the experiment. Be aware the table is per mL!

 

Table I:

 

Day P. caudatum

alone, cells/mL

P. aurelia

alone, cells/mL

P. caudatum

mixed, cells/mL

P. aurelia

mixed, cells/mL

0        
2        
4        
6        
8        
10        
12        
14        
16        

 

 

8. Explain how do you determine when carrying capacity has been reached for a population?

 

 

 

 

 

 

 

 

9. Which organism reached their carrying capacity first?

 

 

 

 

 

 

 

 

 

 

10. How do the population numbers for these organisms compare when they are grown individually versus when they were grown together? Suggest an explanation for any differences.

 

 

 

 

 

 

 

 

 

 

 

 

11. Someone else repeated this experiment many, many times. They found in a few of the samples on Days 10-16 the number of P. caudatum individuals in the mixed culture began to gradually rise. Propose a hypothesis for this observation. You will not be able to look up this answer … you must think about this lab to formulate your answer.

 
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Statistical Biology Lab Report

UTSC Journal of Plant Biology

BIO A01 2018- Fall; 1(1): 1-6

Insert Principal Author’s Name/Student Number

Paper title (The title should be specific and concise-Do not use “Formal Lab Report” in the title. All words except the first word should be in lower case-except for proper nouns.)[endnoteRef:1] [1: Template modified from the following resources: “Manuscript Template,” Science Publishing Group, The Open Access Publisher 2012 URL http://www.sciencepublishinggroup.com/journal/guideforauthors.aspx?journalid=173; Guidelines for Writing Scientific Papers, Honors Organismal Biology Laboratory (no date), URL http://www.bms.bc.ca/resources/library/pdf/GuidelinesScientificPapers.pdf; Guidelines for Writing a Scientific Paper, Maloy 2001, URL http://www.sci.sdsu.edu/~smaloy/MicrobialGenetics/topics/scientific-writing.pdf; and Writing a Scientific Research Paper, Massachusetts Institute of Technology 2000. URL http://umech.mit.edu/freeman/6.021J/2000/writing.pdf. ]

Author’s Name (Principal Author), 1, Author’s Name (Bench-mate 1), 1 Authors Name (Bench-mate 2), 1 Author’s Name (Bench-mate 3), 1 Author’s Name (Bench-mate 4), 1 Author’s Name1 (Bench-mate 5) 1 – If you do not know your bench-mates names, please write your name + 4 other BIOA01 students in PRAXX

1Dept. of Biological Sciences, University of Toronto Scarborough, Toronto, Canada

UTSC BIOA01 Lab PRAXX, BENCHX:

PRAXX TA:

Abstract: An abstract is a one-paragraph summary of your report. It should begin with a few introductory remarks that introduce the significance of the study. It should include (in this order) the background of the study (1-3 sentences), mentioning of the study system/species/object (1 sentence), the question investigated (1 sentence), the general methods used (1 sentence), the principle results (1 sentence) and the conclusions (1 sentence). The reader should be able to determine the major points of your report without having to read further. The language should be concise and no citations should be included in the abstract. The abstract is located at the beginning of your report, however it is usually written once you have finished writing your paper.

Keywords: Include at least 3 keywords or phrases (specific to your paper), which must be separated by commas to differentiate them.

Introduction [Page limit-1 page]

This template is set up to provide you with an example of the format expected for your Formal Lab Report (FLR). The template provides you with the specifications needed for preparing your FLR. You can save this file as a separate document and type your report directly into the template. You can then submit your edited version of this file to Quercus. Please note that Quercus will only accept Word (.docx or .doc) files or PDF (.pdf) files.

The introduction provides a context for the research. This section should include the following: 1) Description of the current state of knowledge or understanding at the beginning of your investigation (i.e., background information synthesized from the existing literature – think about what information readers would need to know to be able to understand your lab report); 2) Background information about study species used; 3) The purpose of the experiment and/or the question being asked; 4) Hypothesis/hypotheses written as statements. Null hypotheses may be included here; 5) Brief description of the approach being used to test your hypothesis/hypotheses statement; 6) Predictions written as explanatory statements (“If…then”) that focus only on experimental treatment groups (not controls) and are backed up with relevant references.

It is imperative that you include properly formatted in-text citations to support all non-original ideas within your introduction. Failure to include in-text citations will result in a grade penalty and could possibly lead to an academic offence.

Materials and Methods [Page limit – 1/2 page- 1 page]

The purpose of this section is to describe the experimental procedures, including any controls. This section should be written in the past tense (and first-person if applicable); the remainder of the paper should be written in the present tense. The description should be complete enough to allow someone to repeat your work. The Methods section should describe the chronological process that you used to complete the research, how all of the data was collected, and a short description of the statistical analyses you completed. It should be written in complete sentences, not bulleted lists. Do not include lab coat, gloves, or safety goggles in your materials description-the use of personal safety equipment is assumed.

Be certain to include any software used to produce graphs and analyze data (e.g., Excel, GraphPad). Also, be certain to include an in-text citation of the lab manual in this section (and a corresponding complete reference in your reference section) but summarize the methods in your own words.

Results [Page limit – 1 ½ – 2 pages (written ½-1 page, figure ½ page, table ½ page)]

The results section describes the results of, but DOES NOT interpret, your experiment. You should present your table and figure in this section. The ‘Results’ section should always begin with text and not your table and figure. You should describe your findings to the reader – you should refer the reader to your table and figure in your results description (e.g., see Table 1 or Figure 1). By referring to your table and figure appropriately, you can concisely present your results in several paragraphs. If you do not refer to the appropriate figure or table in your results section, you will be penalized.

For the purpose of this report, your table and figure should be embedded within your results section. Be certain that there is not a page break in the middle of your table or figure and do not wrap text around the outside of the table and figure. (Note that some journals require that the tables and figures be included following the reference section.) The table caption should appear above the table, whereas the figure caption should appear below the figure. Insert your table and figure after they are cited in the text.

Be sure to record all your class data on the Table 3.2 in your lab manual. You will need these data to do the statistical analysis to produce the Table and Figure for your ‘Results’ section of your Formal Lab Report. See tips for the Table caption below.

Table 1: Your caption should be above your table and include details of what is included in your table. The information in your caption/table should be complete enough and presented in a way that the reader can easily understand the information presented without referring to the text of your report.

INSERT TABLE HERE – Your Statistical Worksheets should not be used for your Table in your Formal Lab Report. You must select information from your Worksheets to make a Table for your FLR. Your Table should include the following columns for each t-test comparison. You will be comparing each of the four treatment groups (light intensity in lumens) with the negative control (dark), as well as the positive control (outside light). Thus, you will have 8 comparisons.

Your Table should include the following columns for each t-test comparison:

a. n

b. critical t- value

c. calculated t-value

d. df

e. actual p-value (p > 0.05 or p < 0.05 or p = 0.05)

f. conclusion (did you reject or fail to reject the null hypothesis?)

INSERT FIGURE HERE – Prepare a bar graph with standard deviation error bars using the total oxygen produced (ml) for your complete data set (posted on Quercus for your lab practical). This means that the columns will be an average of all 8 values for each control and each experimental treatment group. You will have a total of 6 bars in your bar graph. Treatments should be shown as categories on the x- axis, mean total oxygen produced (ml) should be on the y- axis. The controls and the 4 treatments should be discernable by clear labels on the x-axis.

Note: If treatments cannot be discerned from your figure, you will be penalized.

Figure 1: Your caption should be below your figure and include details of what is depicted in your graph. The information in your caption/graph should be complete enough and presented in a way that the reader can easily understand the information presented without referring to the text of your report.

Discussion [Page limit – 1 – 1 ½ pages]

The discussion section is where you report on the interpretation and conclusion of your results. This is your opportunity to demonstrate your ability to analyze, evaluate, interpret and reason effectively. The discussion should relate your findings to your original question, hypothesis (or hypotheses if you had more than one), and predictions, which means that you evaluate your results in terms of your original question/hypothesis/predictions and point out the biological relevance of your findings. Avoid redundancy between the sections, especially the ‘Results’ and ‘Discussion’, of the lab report.

In addition, you should generalize the importance of your findings, discuss ambiguous data, and relate your results to other published studies (i.e., results published in primary scientific literature). Is your work in agreement or in contrast with previously published work? You should also discuss any sources of experimental error or limitations. You should end your discussion by summarizing the main points that you want the reader to remember; you should provide closure for the report and by extension, the reader. You should also recommend specific areas of further research based on your results and the findings of other published studies.

It is imperative that you include properly formatted in-text citations to support all non-original ideas within your discussion. Failure to include in-text citations will result in a major grade penalty.

Acknowledgements [Page limit – 1 paragraph, optional]

The acknowledgements section is where you can choose to acknowledge people who contributed to your work in some way but do not fit the criteria to be included as authors. This is also where you would include information about funding sources.

References [Page limit – 1/2 – 1 page]

You must include at least three primary scientific literature sources (which you are responsible for finding) as well as the BIOA01 lab manual in the proper format (Name-Year System, CSE Style- see Section C of the FLR Information page). Further resources can be included in addition to the three required primary sources. This style combines in-text parenthetical citations with a reference list at the end of your report (Walker and Rapley 2009). The references should be organized in alphabetical order by the primary author’s surname (last name) – DO NOT alphabetize the names within each citation. Be consistent when writing journal titles – write all journal titles out in full (e.g., European Food Research and Technology) or all abbreviated (e.g., Eur Food Res Technol).

Tip: Complete the online Library Research module and associated quiz to help you find relevant primary resources.

See examples below and more by using library resource document included with other FLR files on Quercus. Remember to remove subheadings when preparing your reference list. Reference list should be a single alphabetized list.

Scholarly Journal Article (primary source)

Ma Q, Scanlan C, Bell R, Brennan R. 2013. The dynamics of potassium uptake and use, leaf gas exchange and root growth throughout plant phenological development and its effects on see yield in wheat (Triticum aestivum) on a low-K sandy soil. Plant Soil 373:373-384.

Scholarly Journal Article (primary source found on the internet)

Mattupalli C, Genger RK, Charkowski AO. 2013. Evaluating incidence of Helminthosporium solani and Colletotrichum coccodes on asymptomatic organic potatoes and screening potato lines for resistance to silver scurf. Am J Potato Res [Internet]. [Cited 20 June 2013.] Available from http://link.springer.com/content/pdf/10.1007%2Fs12230-013-9314-3.pdf

Scholarly Journal Article (review, not a primary source)

Miao Y, Stewart BA, Zhang F. 2011. Long-term experiments for sustainable nutrient management in China. A review. Agronomy for Sustainable Development 31:397-414.

Chapter in Book (not a primary source)

Denison RF. 2012. Selfish genes, sophisticated plants, and haphazard ecosystems. In Darwinian Agriculture: How Understanding Evolution can Improve Agriculture. Princeton (NJ): Princeton University Press. Pages 76-94.

Chapter in Book Series (not a primary source)

Fageria NK, Moreira A. 2011. The role of mineral nutrition on root growth of crop plants. Advances in Agronomy (Book series) 110:251-331.

Internet Resource (secondary or tertiary source)

Williamson RC. 2004. Deciduous tree galls [Internet]. Madison (WI): University of Wisconsin-Madison; [cited 2013 Sep 12]. Available from http://labs.russell.wisc.edu/pddc/files/Fact_Sheets/FC_PDF/Deciduous_Tree_Galls.pdf

 
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External Forces And Their Impact On Health Care

External Forces and Their Impact On Health Care

 

Health care quality and safety are not solely dependent on the actions of individual providers and institutions. A host of external forces exert a profound influence on what happens within any single organization or the behavior of any individual provider. These external forces include accreditation bodies, regulators, legislatures, insurers, and many other entities. Sociopolitical forces, including the economy and public opinion, also play a role in how and how well health care is provided.

 

To prepare for this Discussion Question:

 

· Review this week’s Learning Resources.

 

· Choose a specific example of an external force that influences health care and safety, as discussed in Chapter 2 of your Course Text.

 

Then, analyze how it influences health care quality management. (The external force can have minimal or extensive impact on quality.) Finally, evaluate whether the impact on health care is positive or negative, providing evidence to support your position.

 

 

PAPER

 

Pay-for-Performance

 

The predominant model for the delivery of health care in the United States and other parts of the world is fee-for-service. A new model gaining in popularity is known as pay-for-performance, or P4P. In the P4P model, providers are paid for how well they provide care, not how much care they provide. There are rewards for high quality, efficient and effective care and penalties for wastefulness and medical errors. Whether or not P4P can raise the standards of care and/or lower its cost is a matter of some disagreement.

 

To prepare for this Application Assignment:

 

Review the Learning Resources for this week that discuss pay-for for-performance.

Find two additional reputable sources (i.e., news sources, accreditation and health care agencies, peer-reviewed journal articles, etc.) that address the challenges of adopting a pay-for-performance approach for ensuring quality and safety in health care.

 

To complete this Application Assignment, write a 3-page paper that addresses the following:

Summarize and analyze the challenges discussed in the two sources you selected.

Select the two most significant challenges to the successful adoption of a P4P approach, and explain why.

 
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