Example: Factorial design applied in optimisation technique.
To meet the ethical considerations, you need to ensure that.
Collect the data by using suitable data collection according to your experiment’s requirement, such as observations, case studies , surveys , interviews , questionnaires, etc. Analyse the obtained information.
Write the report of your research. Present, conclude, and explain the outcomes of your study .
What is the first step in conducting an experimental research.
The first step in conducting experimental research is to define your research question or hypothesis. Clearly outline the purpose and expectations of your experiment to guide the entire research process.
A dependent variable is one that completely depends on another variable, mostly the independent one.
a simple linear regression is a statistical data technique where two quantitative values are plotted on a graph. The plot is a straight line, which means there’s a direct relationship between the two values.
Struggling with statistical analysis? Here are 7 statistical analysis techniques for beginners performing statistical analysis for the first time.
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Home » Experimental Design – Types, Methods, Guide
Table of Contents
Experimental design is a process of planning and conducting scientific experiments to investigate a hypothesis or research question. It involves carefully designing an experiment that can test the hypothesis, and controlling for other variables that may influence the results.
Experimental design typically includes identifying the variables that will be manipulated or measured, defining the sample or population to be studied, selecting an appropriate method of sampling, choosing a method for data collection and analysis, and determining the appropriate statistical tests to use.
Here are the different types of experimental design:
In this design, participants are randomly assigned to one of two or more groups, and each group is exposed to a different treatment or condition.
This design involves dividing participants into blocks based on a specific characteristic, such as age or gender, and then randomly assigning participants within each block to one of two or more treatment groups.
In a factorial design, participants are randomly assigned to one of several groups, each of which receives a different combination of two or more independent variables.
In this design, each participant is exposed to all of the different treatments or conditions, either in a random order or in a predetermined order.
This design involves randomly assigning participants to one of two or more treatment groups, with each group receiving one treatment during the first phase of the study and then switching to a different treatment during the second phase.
In this design, the researcher manipulates one or more variables at different levels and uses a randomized block design to control for other variables.
This design involves grouping participants within larger units, such as schools or households, and then randomly assigning these units to different treatment groups.
Laboratory experiments are conducted under controlled conditions, which allows for greater precision and accuracy. However, because laboratory conditions are not always representative of real-world conditions, the results of these experiments may not be generalizable to the population at large.
Field experiments are conducted in naturalistic settings and allow for more realistic observations. However, because field experiments are not as controlled as laboratory experiments, they may be subject to more sources of error.
Experimental design methods refer to the techniques and procedures used to design and conduct experiments in scientific research. Here are some common experimental design methods:
This involves randomly assigning participants to different groups or treatments to ensure that any observed differences between groups are due to the treatment and not to other factors.
The use of a control group is an important experimental design method that involves having a group of participants that do not receive the treatment or intervention being studied. The control group is used as a baseline to compare the effects of the treatment group.
Blinding involves keeping participants, researchers, or both unaware of which treatment group participants are in, in order to reduce the risk of bias in the results.
This involves systematically varying the order in which participants receive treatments or interventions in order to control for order effects.
Replication involves conducting the same experiment with different samples or under different conditions to increase the reliability and validity of the results.
This experimental design method involves manipulating multiple independent variables simultaneously to investigate their combined effects on the dependent variable.
This involves dividing participants into subgroups or blocks based on specific characteristics, such as age or gender, in order to reduce the risk of confounding variables.
Experimental design data collection methods are techniques and procedures used to collect data in experimental research. Here are some common experimental design data collection methods:
This method involves observing and recording the behavior or phenomenon of interest in real time. It may involve the use of structured or unstructured observation, and may be conducted in a laboratory or naturalistic setting.
Self-report measures involve asking participants to report their thoughts, feelings, or behaviors using questionnaires, surveys, or interviews. These measures may be administered in person or online.
Behavioral measures involve measuring participants’ behavior directly, such as through reaction time tasks or performance tests. These measures may be administered using specialized equipment or software.
Physiological measures involve measuring participants’ physiological responses, such as heart rate, blood pressure, or brain activity, using specialized equipment. These measures may be invasive or non-invasive, and may be administered in a laboratory or clinical setting.
Archival data involves using existing records or data, such as medical records, administrative records, or historical documents, as a source of information. These data may be collected from public or private sources.
Computerized measures involve using software or computer programs to collect data on participants’ behavior or responses. These measures may include reaction time tasks, cognitive tests, or other types of computer-based assessments.
Video recording involves recording participants’ behavior or interactions using cameras or other recording equipment. This method can be used to capture detailed information about participants’ behavior or to analyze social interactions.
Experimental design data analysis methods refer to the statistical techniques and procedures used to analyze data collected in experimental research. Here are some common experimental design data analysis methods:
Descriptive statistics are used to summarize and describe the data collected in the study. This includes measures such as mean, median, mode, range, and standard deviation.
Inferential statistics are used to make inferences or generalizations about a larger population based on the data collected in the study. This includes hypothesis testing and estimation.
ANOVA is a statistical technique used to compare means across two or more groups in order to determine whether there are significant differences between the groups. There are several types of ANOVA, including one-way ANOVA, two-way ANOVA, and repeated measures ANOVA.
Regression analysis is used to model the relationship between two or more variables in order to determine the strength and direction of the relationship. There are several types of regression analysis, including linear regression, logistic regression, and multiple regression.
Factor analysis is used to identify underlying factors or dimensions in a set of variables. This can be used to reduce the complexity of the data and identify patterns in the data.
SEM is a statistical technique used to model complex relationships between variables. It can be used to test complex theories and models of causality.
Cluster analysis is used to group similar cases or observations together based on similarities or differences in their characteristics.
Time series analysis is used to analyze data collected over time in order to identify trends, patterns, or changes in the data.
Multilevel modeling is used to analyze data that is nested within multiple levels, such as students nested within schools or employees nested within companies.
Experimental design is a versatile research methodology that can be applied in many fields. Here are some applications of experimental design:
Here are some examples of experimental design in different fields:
Experimental research design should be used when a researcher wants to establish a cause-and-effect relationship between variables. It is particularly useful when studying the impact of an intervention or treatment on a particular outcome.
Here are some situations where experimental research design may be appropriate:
Here are the steps to conduct Experimental Research:
The purpose of experimental design is to control and manipulate one or more independent variables to determine their effect on a dependent variable. Experimental design allows researchers to systematically investigate causal relationships between variables, and to establish cause-and-effect relationships between the independent and dependent variables. Through experimental design, researchers can test hypotheses and make inferences about the population from which the sample was drawn.
Experimental design provides a structured approach to designing and conducting experiments, ensuring that the results are reliable and valid. By carefully controlling for extraneous variables that may affect the outcome of the study, experimental design allows researchers to isolate the effect of the independent variable(s) on the dependent variable(s), and to minimize the influence of other factors that may confound the results.
Experimental design also allows researchers to generalize their findings to the larger population from which the sample was drawn. By randomly selecting participants and using statistical techniques to analyze the data, researchers can make inferences about the larger population with a high degree of confidence.
Overall, the purpose of experimental design is to provide a rigorous, systematic, and scientific method for testing hypotheses and establishing cause-and-effect relationships between variables. Experimental design is a powerful tool for advancing scientific knowledge and informing evidence-based practice in various fields, including psychology, biology, medicine, engineering, and social sciences.
Experimental design offers several advantages in research. Here are some of the main advantages:
Experimental design has some limitations that researchers should be aware of. Here are some of the main limitations:
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Experimental design refers to how participants are allocated to different groups in an experiment. Types of design include repeated measures, independent groups, and matched pairs designs.
Probably the most common way to design an experiment in psychology is to divide the participants into two groups, the experimental group and the control group, and then introduce a change to the experimental group, not the control group.
The researcher must decide how he/she will allocate their sample to the different experimental groups. For example, if there are 10 participants, will all 10 participants participate in both groups (e.g., repeated measures), or will the participants be split in half and take part in only one group each?
Three types of experimental designs are commonly used:
Independent measures design, also known as between-groups , is an experimental design where different participants are used in each condition of the independent variable. This means that each condition of the experiment includes a different group of participants.
This should be done by random allocation, ensuring that each participant has an equal chance of being assigned to one group.
Independent measures involve using two separate groups of participants, one in each condition. For example:
Repeated Measures design is an experimental design where the same participants participate in each independent variable condition. This means that each experiment condition includes the same group of participants.
Repeated Measures design is also known as within-groups or within-subjects design .
Suppose we used a repeated measures design in which all of the participants first learned words in “loud noise” and then learned them in “no noise.”
We expect the participants to learn better in “no noise” because of order effects, such as practice. However, a researcher can control for order effects using counterbalancing.
The sample would be split into two groups: experimental (A) and control (B). For example, group 1 does ‘A’ then ‘B,’ and group 2 does ‘B’ then ‘A.’ This is to eliminate order effects.
Although order effects occur for each participant, they balance each other out in the results because they occur equally in both groups.
A matched pairs design is an experimental design where pairs of participants are matched in terms of key variables, such as age or socioeconomic status. One member of each pair is then placed into the experimental group and the other member into the control group .
One member of each matched pair must be randomly assigned to the experimental group and the other to the control group.
Experimental design refers to how participants are allocated to an experiment’s different conditions (or IV levels). There are three types:
1. Independent measures / between-groups : Different participants are used in each condition of the independent variable.
2. Repeated measures /within groups : The same participants take part in each condition of the independent variable.
3. Matched pairs : Each condition uses different participants, but they are matched in terms of important characteristics, e.g., gender, age, intelligence, etc.
Read about each of the experiments below. For each experiment, identify (1) which experimental design was used; and (2) why the researcher might have used that design.
1 . To compare the effectiveness of two different types of therapy for depression, depressed patients were assigned to receive either cognitive therapy or behavior therapy for a 12-week period.
The researchers attempted to ensure that the patients in the two groups had similar severity of depressed symptoms by administering a standardized test of depression to each participant, then pairing them according to the severity of their symptoms.
2 . To assess the difference in reading comprehension between 7 and 9-year-olds, a researcher recruited each group from a local primary school. They were given the same passage of text to read and then asked a series of questions to assess their understanding.
3 . To assess the effectiveness of two different ways of teaching reading, a group of 5-year-olds was recruited from a primary school. Their level of reading ability was assessed, and then they were taught using scheme one for 20 weeks.
At the end of this period, their reading was reassessed, and a reading improvement score was calculated. They were then taught using scheme two for a further 20 weeks, and another reading improvement score for this period was calculated. The reading improvement scores for each child were then compared.
4 . To assess the effect of the organization on recall, a researcher randomly assigned student volunteers to two conditions.
Condition one attempted to recall a list of words that were organized into meaningful categories; condition two attempted to recall the same words, randomly grouped on the page.
Ecological validity.
The degree to which an investigation represents real-life experiences.
These are the ways that the experimenter can accidentally influence the participant through their appearance or behavior.
The clues in an experiment lead the participants to think they know what the researcher is looking for (e.g., the experimenter’s body language).
The variable the experimenter manipulates (i.e., changes) is assumed to have a direct effect on the dependent variable.
Variable the experimenter measures. This is the outcome (i.e., the result) of a study.
All variables which are not independent variables but could affect the results (DV) of the experiment. Extraneous variables should be controlled where possible.
Variable(s) that have affected the results (DV), apart from the IV. A confounding variable could be an extraneous variable that has not been controlled.
Randomly allocating participants to independent variable conditions means that all participants should have an equal chance of taking part in each condition.
The principle of random allocation is to avoid bias in how the experiment is carried out and limit the effects of participant variables.
Changes in participants’ performance due to their repeating the same or similar test more than once. Examples of order effects include:
(i) practice effect: an improvement in performance on a task due to repetition, for example, because of familiarity with the task;
(ii) fatigue effect: a decrease in performance of a task due to repetition, for example, because of boredom or tiredness.
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Neag School of Education
Experimental research.
The major feature that distinguishes experimental research from other types of research is that the researcher manipulates the independent variable. There are a number of experimental group designs in experimental research. Some of these qualify as experimental research, others do not.
The statistics by themselves have no meaning. They only take on meaning within the design of your study. If we just examine stats, bread can be deadly . The term validity is used three ways in research…
There are several common threats to internal validity in experimental research. They are described in our text. I have review each below (this material is also included in the PowerPoint Presentation on Experimental Research for this unit):
When planning a study, it is important to consider the threats to interval validity as we finalize the study design. After we complete our study, we should reconsider each of the threats to internal validity as we review our data and draw conclusions.
Del Siegle, Ph.D. Neag School of Education – University of Connecticut [email protected] www.delsiegle.com
Ever wondered why scientists across the world are being lauded for discovering the Covid-19 vaccine so early? It’s because every…
Ever wondered why scientists across the world are being lauded for discovering the Covid-19 vaccine so early? It’s because every government knows that vaccines are a result of experimental research design and it takes years of collected data to make one. It takes a lot of time to compare formulas and combinations with an array of possibilities across different age groups, genders and physical conditions. With their efficiency and meticulousness, scientists redefined the meaning of experimental research when they discovered a vaccine in less than a year.
Characteristics of experimental research design, types of experimental research design, advantages and disadvantages of experimental research, examples of experimental research.
Experimental research is a scientific method of conducting research using two variables: independent and dependent. Independent variables can be manipulated to apply to dependent variables and the effect is measured. This measurement usually happens over a significant period of time to establish conditions and conclusions about the relationship between these two variables.
Experimental research is widely implemented in education, psychology, social sciences and physical sciences. Experimental research is based on observation, calculation, comparison and logic. Researchers collect quantitative data and perform statistical analyses of two sets of variables. This method collects necessary data to focus on facts and support sound decisions. It’s a helpful approach when time is a factor in establishing cause-and-effect relationships or when an invariable behavior is seen between the two.
Now that we know the meaning of experimental research, let’s look at its characteristics, types and advantages.
The hypothesis is at the core of an experimental research design. Researchers propose a tentative answer after defining the problem and then test the hypothesis to either confirm or disregard it. Here are a few characteristics of experimental research:
Experimental research is equally effective in non-laboratory settings as it is in labs. It helps in predicting events in an experimental setting. It generalizes variable relationships so that they can be implemented outside the experiment and applied to a wider interest group.
The way a researcher assigns subjects to different groups determines the types of experimental research design .
In a pre-experimental research design, researchers observe a group or various groups to see the effect an independent variable has on the dependent variable to cause change. There is no control group as it is a simple form of experimental research . It’s further divided into three categories:
This design is practical but lacks in certain areas of true experimental criteria.
This design depends on statistical analysis to approve or disregard a hypothesis. It’s an accurate design that can be conducted with or without a pretest on a minimum of two dependent variables assigned randomly. It is further classified into three types:
True experimental research design should have a variable to manipulate, a control group and random distribution.
With experimental research, we can test ideas in a controlled environment before marketing. It acts as the best method to test a theory as it can help in making predictions about a subject and drawing conclusions. Let’s look at some of the advantages that make experimental research useful:
Even though it’s a scientific method, it has a few drawbacks. Here are a few disadvantages of this research method:
Experimental research design is a sophisticated method that investigates relationships or occurrences among people or phenomena under a controlled environment and identifies the conditions responsible for such relationships or occurrences
Experimental research can be used in any industry to anticipate responses, changes, causes and effects. Here are some examples of experimental research :
Experimental research is considered a standard method that uses observations, simulations and surveys to collect data. One of its unique features is the ability to control extraneous variables and their effects. It’s a suitable method for those looking to examine the relationship between cause and effect in a field setting or in a laboratory. Although experimental research design is a scientific approach, research is not entirely a scientific process. As much as managers need to know what is experimental research , they have to apply the correct research method, depending on the aim of the study.
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The purpose of study, experimental, or research design in scientific manuscripts has changed significantly over the years. It has evolved from an explanation of the design of the experiment (ie, data gathering or acquisition) to an explanation of the statistical analysis. This practice makes “Methods” sections hard to read and understand.
To clarify the difference between study design and statistical analysis, to show the advantages of a properly written study design on article comprehension, and to encourage authors to correctly describe study designs.
The role of study design is explored from the introduction of the concept by Fisher through modern-day scientists and the AMA Manual of Style . At one time, when experiments were simpler, the study design and statistical design were identical or very similar. With the complex research that is common today, which often includes manipulating variables to create new variables and the multiple (and different) analyses of a single data set, data collection is very different than statistical design. Thus, both a study design and a statistical design are necessary.
Scientific manuscripts will be much easier to read and comprehend. A proper experimental design serves as a road map to the study methods, helping readers to understand more clearly how the data were obtained and, therefore, assisting them in properly analyzing the results.
Study, experimental, or research design is the backbone of good research. It directs the experiment by orchestrating data collection, defines the statistical analysis of the resultant data, and guides the interpretation of the results. When properly described in the written report of the experiment, it serves as a road map to readers, 1 helping them negotiate the “Methods” section, and, thus, it improves the clarity of communication between authors and readers.
A growing trend is to equate study design with only the statistical analysis of the data. The design statement typically is placed at the end of the “Methods” section as a subsection called “Experimental Design” or as part of a subsection called “Data Analysis.” This placement, however, equates experimental design and statistical analysis, minimizing the effect of experimental design on the planning and reporting of an experiment. This linkage is inappropriate, because some of the elements of the study design that should be described at the beginning of the “Methods” section are instead placed in the “Statistical Analysis” section or, worse, are absent from the manuscript entirely.
Have you ever interrupted your reading of the “Methods” to sketch out the variables in the margins of the paper as you attempt to understand how they all fit together? Or have you jumped back and forth from the early paragraphs of the “Methods” section to the “Statistics” section to try to understand which variables were collected and when? These efforts would be unnecessary if a road map at the beginning of the “Methods” section outlined how the independent variables were related, which dependent variables were measured, and when they were measured. When they were measured is especially important if the variables used in the statistical analysis were a subset of the measured variables or were computed from measured variables (such as change scores).
The purpose of this Communications article is to clarify the purpose and placement of study design elements in an experimental manuscript. Adopting these ideas may improve your science and surely will enhance the communication of that science. These ideas will make experimental manuscripts easier to read and understand and, therefore, will allow them to become part of readers' clinical decision making.
The terms study design, experimental design, and research design are often thought to be synonymous and are sometimes used interchangeably in a single paper. Avoid doing so. Use the term that is preferred by the style manual of the journal for which you are writing. Study design is the preferred term in the AMA Manual of Style , 2 so I will use it here.
A study design is the architecture of an experimental study 3 and a description of how the study was conducted, 4 including all elements of how the data were obtained. 5 The study design should be the first subsection of the “Methods” section in an experimental manuscript (see the Table ). “Statistical Design” or, preferably, “Statistical Analysis” or “Data Analysis” should be the last subsection of the “Methods” section.
Table. Elements of a “Methods” Section
The “Study Design” subsection describes how the variables and participants interacted. It begins with a general statement of how the study was conducted (eg, crossover trials, parallel, or observational study). 2 The second element, which usually begins with the second sentence, details the number of independent variables or factors, the levels of each variable, and their names. A shorthand way of doing so is with a statement such as “A 2 × 4 × 8 factorial guided data collection.” This tells us that there were 3 independent variables (factors), with 2 levels of the first factor, 4 levels of the second factor, and 8 levels of the third factor. Following is a sentence that names the levels of each factor: for example, “The independent variables were sex (male or female), training program (eg, walking, running, weight lifting, or plyometrics), and time (2, 4, 6, 8, 10, 15, 20, or 30 weeks).” Such an approach clearly outlines for readers how the various procedures fit into the overall structure and, therefore, enhances their understanding of how the data were collected. Thus, the design statement is a road map of the methods.
The dependent (or measurement or outcome) variables are then named. Details of how they were measured are not given at this point in the manuscript but are explained later in the “Instruments” and “Procedures” subsections.
Next is a paragraph detailing who the participants were and how they were selected, placed into groups, and assigned to a particular treatment order, if the experiment was a repeated-measures design. And although not a part of the design per se, a statement about obtaining written informed consent from participants and institutional review board approval is usually included in this subsection.
The nuts and bolts of the “Methods” section follow, including such things as equipment, materials, protocols, etc. These are beyond the scope of this commentary, however, and so will not be discussed.
The last part of the “Methods” section and last part of the “Study Design” section is the “Data Analysis” subsection. It begins with an explanation of any data manipulation, such as how data were combined or how new variables (eg, ratios or differences between collected variables) were calculated. Next, readers are told of the statistical measures used to analyze the data, such as a mixed 2 × 4 × 8 analysis of variance (ANOVA) with 2 between-groups factors (sex and training program) and 1 within-groups factor (time of measurement). Researchers should state and reference the statistical package and procedure(s) within the package used to compute the statistics. (Various statistical packages perform analyses slightly differently, so it is important to know the package and specific procedure used.) This detail allows readers to judge the appropriateness of the statistical measures and the conclusions drawn from the data.
Avoid using the term statistical design . Statistical methods are only part of the overall design. The term gives too much emphasis to the statistics, which are important, but only one of many tools used in interpreting data and only part of the study design:
The most important issues in biostatistics are not expressed with statistical procedures. The issues are inherently scientific, rather than purely statistical, and relate to the architectural design of the research, not the numbers with which the data are cited and interpreted. 6
Stated another way, “The justification for the analysis lies not in the data collected but in the manner in which the data were collected.” 3 “Without the solid foundation of a good design, the edifice of statistical analysis is unsafe.” 7 (pp4–5)
The intertwining of study design and statistical analysis may have been caused (unintentionally) by R.A. Fisher, “… a genius who almost single-handedly created the foundations for modern statistical science.” 8 Most research did not involve statistics until Fisher invented the concepts and procedures of ANOVA (in 1921) 9 , 10 and experimental design (in 1935). 11 His books became standard references for scientists in many disciplines. As a result, many ANOVA books were titled Experimental Design (see, for example, Edwards 12 ), and ANOVA courses taught in psychology and education departments included the words experimental design in their course titles.
Before the widespread use of computers to analyze data, designs were much simpler, and often there was little difference between study design and statistical analysis. So combining the 2 elements did not cause serious problems. This is no longer true, however, for 3 reasons: (1) Research studies are becoming more complex, with multiple independent and dependent variables. The procedures sections of these complex studies can be difficult to understand if your only reference point is the statistical analysis and design. (2) Dependent variables are frequently measured at different times. (3) How the data were collected is often not directly correlated with the statistical design.
For example, assume the goal is to determine the strength gain in novice and experienced athletes as a result of 3 strength training programs. Rate of change in strength is not a measurable variable; rather, it is calculated from strength measurements taken at various time intervals during the training. So the study design would be a 2 × 2 × 3 factorial with independent variables of time (pretest or posttest), experience (novice or advanced), and training (isokinetic, isotonic, or isometric) and a dependent variable of strength. The statistical design , however, would be a 2 × 3 factorial with independent variables of experience (novice or advanced) and training (isokinetic, isotonic, or isometric) and a dependent variable of strength gain. Note that data were collected according to a 3-factor design but were analyzed according to a 2-factor design and that the dependent variables were different. So a single design statement, usually a statistical design statement, would not communicate which data were collected or how. Readers would be left to figure out on their own how the data were collected.
With the advent of electronic data gathering and computerized data handling and analysis, research projects have increased in complexity. Many projects involve multiple dependent variables measured at different times, and, therefore, multiple design statements may be needed for both data collection and statistical analysis. Consider, for example, a study of the effects of heat and cold on neural inhibition. The variables of H max and M max are measured 3 times each: before, immediately after, and 30 minutes after a 20-minute treatment with heat or cold. Muscle temperature might be measured each minute before, during, and after the treatment. Although the minute-by-minute data are important for graphing temperature fluctuations during the procedure, only 3 temperatures (time 0, time 20, and time 50) are used for statistical analysis. A single dependent variable H max :M max ratio is computed to illustrate neural inhibition. Again, a single statistical design statement would tell little about how the data were obtained. And in this example, separate design statements would be needed for temperature measurement and H max :M max measurements.
As stated earlier, drawing conclusions from the data depends more on how the data were measured than on how they were analyzed. 3 , 6 , 7 , 13 So a single study design statement (or multiple such statements) at the beginning of the “Methods” section acts as a road map to the study and, thus, increases scientists' and readers' comprehension of how the experiment was conducted (ie, how the data were collected). Appropriate study design statements also increase the accuracy of conclusions drawn from the study.
The goal of scientific writing, or any writing, for that matter, is to communicate information. Including 2 design statements or subsections in scientific papers—one to explain how the data were collected and another to explain how they were statistically analyzed—will improve the clarity of communication and bring praise from readers. To summarize:
Thanks to Thomas A. Cappaert, PhD, ATC, CSCS, CSE, for suggesting the link between R.A. Fisher and the melding of the concepts of research design and statistics.
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Methodology
Research methods are specific procedures for collecting and analyzing data. Developing your research methods is an integral part of your research design . When planning your methods, there are two key decisions you will make.
First, decide how you will collect data . Your methods depend on what type of data you need to answer your research question :
Second, decide how you will analyze the data .
Methods for collecting data, examples of data collection methods, methods for analyzing data, examples of data analysis methods, other interesting articles, frequently asked questions about research methods.
Data is the information that you collect for the purposes of answering your research question . The type of data you need depends on the aims of your research.
Your choice of qualitative or quantitative data collection depends on the type of knowledge you want to develop.
For questions about ideas, experiences and meanings, or to study something that can’t be described numerically, collect qualitative data .
If you want to develop a more mechanistic understanding of a topic, or your research involves hypothesis testing , collect quantitative data .
Qualitative | to broader populations. . | |
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Quantitative | . |
You can also take a mixed methods approach , where you use both qualitative and quantitative research methods.
Primary research is any original data that you collect yourself for the purposes of answering your research question (e.g. through surveys , observations and experiments ). Secondary research is data that has already been collected by other researchers (e.g. in a government census or previous scientific studies).
If you are exploring a novel research question, you’ll probably need to collect primary data . But if you want to synthesize existing knowledge, analyze historical trends, or identify patterns on a large scale, secondary data might be a better choice.
Primary | . | methods. |
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Secondary |
In descriptive research , you collect data about your study subject without intervening. The validity of your research will depend on your sampling method .
In experimental research , you systematically intervene in a process and measure the outcome. The validity of your research will depend on your experimental design .
To conduct an experiment, you need to be able to vary your independent variable , precisely measure your dependent variable, and control for confounding variables . If it’s practically and ethically possible, this method is the best choice for answering questions about cause and effect.
Descriptive | . . | |
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Experimental |
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Research method | Primary or secondary? | Qualitative or quantitative? | When to use |
---|---|---|---|
Primary | Quantitative | To test cause-and-effect relationships. | |
Primary | Quantitative | To understand general characteristics of a population. | |
Interview/focus group | Primary | Qualitative | To gain more in-depth understanding of a topic. |
Observation | Primary | Either | To understand how something occurs in its natural setting. |
Secondary | Either | To situate your research in an existing body of work, or to evaluate trends within a research topic. | |
Either | Either | To gain an in-depth understanding of a specific group or context, or when you don’t have the resources for a large study. |
Your data analysis methods will depend on the type of data you collect and how you prepare it for analysis.
Data can often be analyzed both quantitatively and qualitatively. For example, survey responses could be analyzed qualitatively by studying the meanings of responses or quantitatively by studying the frequencies of responses.
Qualitative analysis is used to understand words, ideas, and experiences. You can use it to interpret data that was collected:
Qualitative analysis tends to be quite flexible and relies on the researcher’s judgement, so you have to reflect carefully on your choices and assumptions and be careful to avoid research bias .
Quantitative analysis uses numbers and statistics to understand frequencies, averages and correlations (in descriptive studies) or cause-and-effect relationships (in experiments).
You can use quantitative analysis to interpret data that was collected either:
Because the data is collected and analyzed in a statistically valid way, the results of quantitative analysis can be easily standardized and shared among researchers.
Research method | Qualitative or quantitative? | When to use |
---|---|---|
Quantitative | To analyze data collected in a statistically valid manner (e.g. from experiments, surveys, and observations). | |
Meta-analysis | Quantitative | To statistically analyze the results of a large collection of studies. Can only be applied to studies that collected data in a statistically valid manner. |
Qualitative | To analyze data collected from interviews, , or textual sources. To understand general themes in the data and how they are communicated. | |
Either | To analyze large volumes of textual or visual data collected from surveys, literature reviews, or other sources. Can be quantitative (i.e. frequencies of words) or qualitative (i.e. meanings of words). |
If you want to know more about statistics , methodology , or research bias , make sure to check out some of our other articles with explanations and examples.
Research bias
Quantitative research deals with numbers and statistics, while qualitative research deals with words and meanings.
Quantitative methods allow you to systematically measure variables and test hypotheses . Qualitative methods allow you to explore concepts and experiences in more detail.
In mixed methods research , you use both qualitative and quantitative data collection and analysis methods to answer your research question .
A sample is a subset of individuals from a larger population . Sampling means selecting the group that you will actually collect data from in your research. For example, if you are researching the opinions of students in your university, you could survey a sample of 100 students.
In statistics, sampling allows you to test a hypothesis about the characteristics of a population.
The research methods you use depend on the type of data you need to answer your research question .
Methodology refers to the overarching strategy and rationale of your research project . It involves studying the methods used in your field and the theories or principles behind them, in order to develop an approach that matches your objectives.
Methods are the specific tools and procedures you use to collect and analyze data (for example, experiments, surveys , and statistical tests ).
In shorter scientific papers, where the aim is to report the findings of a specific study, you might simply describe what you did in a methods section .
In a longer or more complex research project, such as a thesis or dissertation , you will probably include a methodology section , where you explain your approach to answering the research questions and cite relevant sources to support your choice of methods.
Other students also liked, writing strong research questions | criteria & examples.
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Celebrating the Milestone of Fusion Ignition
In 2022, Lawrence Livermore National Laboratory made history by demonstrating fusion ignition for the first time in a laboratory setting. Read about the people, facilities, capabilities and decades of tenacity that made this achievement possible.
Read about our fusion breakthrough
Joe Ralph, co-lead author and inertial confinement fusion research physicist at Lawrence Livermore National Laboratory, discusses the critical role of implosion symmetry in achieving a burning plasma state at the National Ignition Facility. (Photo: Blaise Douros/LLNL)
Time-integrated X-ray images of the “hot spot” used to infer mode-2 symmetry and mix fraction.
Researchers at Lawrence Livermore National Laboratory (LLNL) have retrospectively confirmed that implosion asymmetry was a major aspect for fusion experiments before achieving ignition for the first time at the Lab’s National Ignition Facility (NIF), the world’s most energetic laser.
The findings were recently detailed in a Nature Communications paper titled “The impact of low-mode symmetry on inertial fusion energy output in the burning plasma state.” The study was co-led by LLNL inertial confinement fusion (ICF) research physicists Joe Ralph, Steven Ross and Alex Zylstra, the former lead of the Hybrid-E ICF campaign.
In 2021, indirect drive ICF experiments achieved a burning plasma state with neutron yields exceeding 170 kJ, roughly three times the record in 2019 and a necessary stage for igniting plasmas. The results were achieved despite multiple sources of degradations — including asymmetries — that lead to high variability in performance. This milestone was a critical step toward achieving ignition on Dec. 5, 2022, Ralph said.
The significance of symmetry in ICF experiments, Ralph said, is like trying to fly an airplane with a heavy left wing. The relative wing weight doesn’t matter much while you are still on the ground, but it makes a big difference when you try to lift off. Achieving a burning plasma is like lifting off.
“Reaching a burning plasma state was a pivotal moment for us,” Ralph said. “It validated years of theoretical and experimental work and provided a solid foundation for future advancements.”
For the first time, the paper presents an empirical degradation factor for mode-2 asymmetry in the burning plasma regime, in addition to previously determined degradations of radiative mix and mode-1 asymmetry. The analysis demonstrates that incorporating these three degradations into the theoretical fusion yield scaling developed in 2017-2018 accounts for the measured fusion performance variability in the two highest-performing experimental campaigns on the NIF to within error.
“In our fusion experiments, achieving symmetry is crucial,” Ralph said. “If the plasma is not uniformly compressed, the energy is not efficiently contained, then the performance suffers. By understanding and correcting these asymmetries, we can ensure that the conditions are just right for ignition, much like making sure your airplane is properly balanced before taking off.”
The paper highlights how the team quantified the performance sensitivity to mode-2 asymmetry in the burning plasma regime and applied the results, in the form of an empirical degradation factor, to a 1D fusion performance model. Additionally, the team determined through a series of integrated 2D radiation hydrodynamic simulations that the sensitivity to mode-2 was consistent with the experimentally determined sensitivity only when including alpha-heating.
“By isolating and quantifying the mode-2 degradation, we were able to refine our models and improve the accuracy of our predictions,” Ralph said. “These findings underscore the importance of continuous refinement and understanding of the variables affecting fusion performance. By identifying and accounting for these degradation factors, we have been better able to assess the performance of our experiments and make more informed decisions. This was a significant step toward achieving ignition.”
Click here for a complete list of authors.
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BMC Veterinary Research volume 20 , Article number: 351 ( 2024 ) Cite this article
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Probiotics are becoming increasingly popular as eco-friendly alternatives in aquaculture. However, there is limited research on their impacts on the reproductive efficiency of Red Tilapia ( Oreochromis niloticus x O. mossambicus ) broodstock. Therefore, this experiment aimed to explore the combined effects of selective probiotics Bacillus subtilis and B. licheniformis (BSL; 1:1) added to water on blood hematology, serum metabolites, gonadal histology, reproductive performance, and reproductive associated genes in Red Tilapia broodstock. Tilapia broodfish weighing 140–160 g were stocked in four treatment groups: control (T0), and the other three groups were added different levels of BSL to the water as follows: T1 (0.01 g/m 3 ), T2 (0.02 g/m 3 ), and T3 (0.03 g/m 3 ), respectively. Results indicate that BSL administration significantly improved RBCs, hemoglobin, hematocrit, MCH, and MCHC, with the highest improvement seen in the T3 group ( P < 0.05). BSL added to the fish water significantly enhanced serum protein fractions (total protein, albumin, and globulins), while AST, ALT, ALP, creatinine, uric acid, and glucose were significantly diminished in a dose-dependent way ( P < 0.05). Adding 0.02–0.03 g/ m 3 of BSL resulted in higher antioxidant status (superoxide dismutase and catalase) compared to other groups ( P < 0.05). Testosterone levels were higher in T3 than in other groups ( P < 0.05). All female hormones (LH, FSH, estradiol, and progesterone) were substantially augmented by the addition of BSL. Additionally, the BSL groups exhibited higher GSI, HSI, VSI (male only), egg diameter (mm), mean number of fry/fish, and mean fry weight (g) compared to the control group ( P < 0.05). Expression of reproductive-associated genes ( vasa , nanos1a , nanos2 , dnd1 , pum1 , AMH , and vtg ) were significantly up-regulated in the gonads of fish in the 0.03 g/m 3 treatment. The histological gonadal structure exhibited that BSL improved gonad maturation in both genders of Tilapia fish. Overall, adding a mixture of B. subtilis and B. licheniformis (0.03 g/m 3 water) can accelerate reproductive performance in Red Tilapia through up-regulation of reproductive genes and enhance the health profile.
Peer Review reports
Aquaculture’s sustainability depends on the effective utilization of aquafeeds and the implementation of robust aquaculture health management practices. Aquaculture contributes to approximately 50% of the world’s total fish production, solidifying its position as the fastest-growing sector within the industry [ 1 , 2 ]. Moreover, it plays a significant part in providing sustainable income opportunities and contributing to global food security [ 3 ]. In Egypt, there are numerous fish species that inhabit its water resources. The country’s diverse aquatic ecosystems support a wide variety of fish, including Nile tilapia, catfish, and mullet [ 4 ]. These fish play a crucial role in the local economy and provide a vital source of protein for the population. The aquaculture industry in Egypt is an important sector that contributes to the country’s food security and economic development. However, local production rarely meets domestic demand, leading the country to rely on imports to cover the shortage [ 2 ]. Tilapias are a globally farmed group of fish, with a production of approximately 6.7 million tons in 2023. This industry is valued at over 14.1 billion US dollars [ 5 ]. As omnivorous fish, tilapias can host both beneficial and harmful bacteria in their gastrointestinal tract, culture water, and sediment. Some examples of bacteria found in the gastrointestinal tract of Nile Tilapia fish include Lactobacillus farciminis , Lactobacillus coryniformis , Lactobacillus brevis , Lactobacillus collinoides , Bacillus sp., and others. Bacillus sp., P. Fluorescens , L. brevis , and L. collinoides are commonly abundant in the fish’s gut [ 3 , 6 ].
Probiotics have emerged as a promising alternative strategy for preventing infectious diseases [ 7 , 8 ]. In aquaculture, probiotics offer numerous benefits, such as improving water quality, enhancing digestion, and boosting fish growth and immune response [ 9 , 10 , 11 ]. Probiotics can enhance feed efficiency in aquatic animals by increasing the activity of digestive enzymes and maintaining a healthy balance of intestinal microbes. This leads to better nutrient absorption and utilization, as well as improved reproductive system function [ 12 , 13 ]. Probiotic supplementation also increases appetite and the digestibility of organisms [ 9 ]. B. subtilis and B. licheniformis bacteria are important probiotic additives for maintaining the normal growth and functions of aquatic animals’ by providing vitamins, nutrients, and producing digestive enzymes. These factors positively effects on feed utilization, nutritional absorption, and growth performance [ 14 ]. Bacillus spp. have various positive ways, such as promoting better nutrient utilization, production and secretion of exogenous enzymes, and enhancing gut microbiota to support intestinal physiological functions [ 10 , 15 , 16 ]. Therefore, fishes fed with different Bacillus species have shown improve growth indices [ 17 ]. Additionally, altering the harmful intestinal microbiota composition to favour a greater proportion of beneficial bacterial communities can support adaptive and innate functions and promote intestinal integrity in the host [ 3 ].
Probiotic mechanisms include actions to inhibit pathogen growth, production of various ingredients (e.g., organic acids, bacteriocins, and volatile compounds), competition for adherence sites and nutrients [ 18 , 19 ], and enhancement of innate immune responses (e.g., respiratory burst activities, lysozyme enhancement) and interactions with natural killer cells, leukocytes, and phagocytes [ 11 , 19 ]. An appropriate and balanced diet not only provides the principal and necessary components for better fish growth but also commonly includes feed supplements such as herbal extracts, probiotics, and symbiotics to boost the immune system and growth rate [ 17 ]. Probiotic addition has been shown to enhance antioxidant capacity, digestive enzymes, and immune function in Nile tilapia fish [ 6 , 8 , 20 ]. Additionally, both serum and mucosal surfaces’ immunoglobulin M (IgM) levels have been found to play an essential role in defending against numerous pathogenic organisms that infect cultured fish [ 21 , 22 ]. One important attribute of Bacillus species is their ability to form spores, which allows them to withstand the heat generated during feed palletization [ 16 , 17 , 23 ]. These spores also enable the bacteria to survive the adverse environment of the fish’s stomach and colonize the intestines, where they can multiply and produce various beneficial digestive enzymes such as amylase, lipase, and protease [ 23 , 24 , 25 ]. Additionally, probiotics’ molecular mechanism of action involves influencing the expression and regulation of different genes [ 15 , 26 , 27 ]. Therefore, the authors of the current study discovered that increasing levels of B. subtilis and B. licheniformis have many substantially beneficial consequences on the physiology, blood health and reproductive performance of red tilapia. With this backdrop, the experiment was conducted to determine the effect of graded levels of water probiotics, B. subtilis and B. licheniformis on hematological variables, reproductive ability, and expression of reproductive-related genes in Red Tilapia broodstock ( O. niloticus x O. mossambicus ).
Fish and experimental design.
This experiment was performed at the Fish Research Centre, Arish University, North Sinai, Egypt. Adult male and female hybrid red tilapia ( O. niloticus x O. mossambicus ) weighing 140–160 g were housed in concrete tanks with a volume of 3 × 4 × 0.8 m³. A total of 480 fish were used in this experiment. The fish were divided into four groups, with each treatment consisting of 120 fish (three tanks, 40 fish in each tank). The fish were stocked in triplicates at a ratio of 1 male to 3 females per cubic meter, with a total density of forty fish per tank (around 860 g/m 3 ). The fish were acclimated to the trial culture conditions for fifteen days. Air stones were provided in the tanks throughout the trial, and a light cycle of 12 h light and 12 h dark was maintained. Four treatments were included: a control group (T0), and three groups (T1, T2 and T3) with varying levels of B. subtilis and B. licheniformis added to the water. The treatment fish groups (2.5% of the total biomass) were labeled as follows: T0 (0 g/m 3 ), T1 (0.01 g/m 3 ), T2 (0.02 g/m 3 ), and T3 (0.03 g/m 3 ). The fish were fed an extruded diet from ALLER AQUA FEED ( https://www.aller-aqua.com/ ) with 30% crude protein, 5.2% crude fat, 5.8% total ash, and 4.8% crude fiber. Each morning, before the first feeding, the fish feces and waste were siphoned, and approximately 10% of the pond water was replaced with dechlorinated water of similar temperature. Every day, the doses of B. subtilis and B. licheniformis were adjusted according to the rate of water changes. At the end of the experiment, the fish from each tank were collected, tallied, weighed, and the weights and survival rate were documented. The fishpond was then cleaned, and the fish were prepared for the spawning period. Thirty ripe females and ten ripe males were placed in the culture tanks for 20 days. During this period, the reproduction capability and spawning performance were measured.
The water elements such as salinity (g/L), temperature (°C), pH, dissolved oxygen (DO, mg/L), total ammonia nitrogen (TAN, mg/L), and ammonia (mg/L) were monitored twice a week employing the YSI-556 multi-parameter method (YSI Inc., Yellow Springs, OH, USA) to assess water quality.
Before the final harvest, all fish were fasted for approximately 12 h. Subsequently,5 fish per tank were anesthetized using amino-benzoic acid (120 mg/L, Sigma-Aldrich, Germany) for blood sample collection. The blood samples were obtained for hemato-biochemical and other physiological parameters. Blood samples were captured from the caudal vein using sterilized needles and separated into subsamples. The first part was stored in heparinized tubes for the hematology parameters analysis. While, the second part was stored in non-heparinized tubes and left to coagulate at room temperature, following the method described by [ 25 ] for serum separation. The blood was then centrifuged at 4000 rpm for 10 min to separate the serum, which was subsequently stored at -20 °C for further analysis.
Red blood cells (RBCs) were counted using the method described by [ 28 ] with a Bright-Line Hemocytometer (Neubauer enhanced, Germany). Hemoglobin (Hb) levels were measured calorimetrically, as outlined by [ 29 ]. Hematocrit (Hct) was calculated following the method of [ 30 ]. The levels of MCV (mean corpuscular volume), MCHC (mean corpuscular hemoglobin concentration), and MCH (mean corpuscular hemoglobin) were determined according to [ 28 ].
The serum total protein fraction (total protein and albumin) was determined using kits provided by Diamond Diagnostics Company. Globulin concentration was calculated using the difference method between total protein and albumin. Kidney related biomarkers such as uric acid, creatinine, and urea were assess according to the method of [ 31 ] using kits provided by Biocompare company (South San Francisco, United States). Glucose levels were determined by the colorimetric glucose oxidase technique of [ 32 ]. The activities of ALT (alanine aminotransferase), AST (aspartate aminotransferase), and ALP (alkaline phosphatase) were measured using an automated analyzer (Abbott Alcyon 300, USA) in accordance with the Pars Azmon Kit’s protocol (Pars Azmon, Iran). The “hydroxylamine method” was used to determine superoxide dismutase (SOD) activity [ 33 ], while the “visible light method” used for catalase (CAT) activity [ 34 ]. Steroid female hormones such as estradiol (E2, MBS700179), progesterone (P, MBS2602842), luteinizing (LH, MBS283097), and follicle-stimulating (FSH, MBS281137) hormones were determined using commercial ELISA kits as explained by [ 35 ]. Testosterone (T, MBS933475) hormone was assessed using quantitative competitive method by ELISA kit. All kits used for steroids hormones were provided by the MyBiosource company (San Diego, USA).
The total body length (T.L) in centimeters and weight (W) in grams were recorded for 30 fish in each group (15 males and 15 females). The liver, gut, and gonads of 30 fish (5 males and 5 females/ tank) per group were removed and weighed. The hepatosomatic index (HSI), viscerasomatic index (VSI), and gonadosomatic index (GSI) were calculated using the following equations:
For 20 days, the spawning performance was monitored. Five gravid, spawn-ready females were eliminated from all tanks, gently stripped, and then subsamples of around ten eggs were randomly selected for determining the diameter of eggs (mm) [ 36 ]. Each female was returned to the appropriate tank after stripping until the end of the trial. Females in each tank were checked daily to find eggs or fry. The eggs were left in the females’ mouths until hatching and complete yolk sac absorption. The fry were then gathered from their respective females, counted, and weighed; the averages were evaluated following the method described by [ 37 ] method. By distributing the total quantity of fry in the tank by the number of female spawns, the mean number of fry per spawning was determined.
Cdna production and total rna extraction.
Samples of testes and ovaries were collected and frozen using liquid nitrogen to analyze the expression of various reproduction-related genes. Each 50 mg of ovarian and testicular tissues was used for RNA extraction with Trizol reagent (iNtRON Biotechnology, Inc., South Korea). The RNA concentration was determined using a NanoDrop method (UV-Vis spectrophotometer, USA). The cDNA was synthesized with the Fast HiSenScript TM RH RT PreMix cDNA synthesis kit (iNtRON Biotechnology, South Korea), and the samples were kept at -20 °C for further analysis.
The specific primer sequences, product sizes, and GenBank accession numbers of reproduction-associated genes, namely vasa , nanos1a , nanos2a , dnd1 , pum1 , AMH , and vtg for both males and females, are listed in Table 1 . The Elf1α gene served as a housekeeping (reference) gene for normalizing mRNA expressions. RT-PCR was performed using the SYBR Green PCR Master Mix to quantify the mRNA expression of the target genes (SensiFast™ SYBR Lo-Rox kit, Bioline). The thermocycling settings were as follows: 95 °C for 10 min, followed by 40 cycles at 94 °C for 15s, 60 °C for 1 min, and 72 °C for 20 s. The mRNA expression levels of each gene were normalized and standardized to the mRNA of elf1α transcripts using the 2 −ΔΔCT approach [ 38 ].
The testes and ovaries of males and females were freshly removed, fixed in neutral formaldehyde (10%) for 24 h, then dehydrated with graded ethanol, and immersed in methyl benzoate for 24 h. They were then cleared in xylene, embedded in purified paraffin wax, and sectioned to a thickness of 5–7 μm using an automated microtome. The sectioned tissues were stained with hematoxylin and eosin and examined under a light microscope (Zeiss) using the method described by [ 39 ].
Results are presented as means ± standard error (S.E.). All numerical data were checked for homogeneity of variance using Levene’s test and for normality of distribution using the Shapiro-Wilk test. The data were analyzed using SPSS software (Version 26.0; SPSS, Chicago, IL, USA) through a one-way analysis of variance (ANOVA) to determine statistical significance at a 95% confidence level. If the F values from the ANOVA test were found to be significant ( P < 0.05), Duncan’s multiple range test was also used to compare means.
The administration of BSL significantly improved water quality variables ( P < 0.05; Table 2 ). Total ammonia nitrogen (TAN) and NH 3 values were reduced in a dose-dependent manner ( P < 0.05) with the most significant decrease observed in T3. The pH values were significantly lower in the T2 and T3 treatments compared to other treatments ( P < 0.05). Salinity levels did not vary among the groups ( P > 0.05). T3 revealed lower dissolved oxygen (DO) levels compared to other groups ( P < 0.05).
The impact of various doses of BSL (0.01, 0.02, and 0.03 g/m 3 ) on hemato-biochemical parameters is shown in Table 3 . The results show a significant increase in RBC counts, Hb, and Hct in T3 ( P < 0.05) compared to other groups. MCV did not show a significant change ( P > 0.05) with the addition of probiotics. In contrast, MCH and MCHC values were substantially increased ( P < 0.05) in T3, with MCHC reaching its maximum value in this treatment. Besides, the highest values of albumin, total protein, and globulin ( P < 0.05) were obtained in the B. subtilis and B. licheniformis (0.03 g/m 3 ) treatment.
The hepatic function enzymes ALT, AST, and ALP were notably affected ( P < 0.05) by the addition of BSL, with higher levels observed in the untreated group compared to other treatments. The probiotics-treated groups shown lower values for ALP, AST, and ALT than the control group ( P < 0.05), indicating improved liver function. Similar trends were observed for creatinine, urea, and uric acid ( P < 0.05), suggesting that probiotics enhanced overall fish health. In terms of antioxidant enzymes CAT and SOD, there was a significant increase ( P < 0.05) with higher levels of B. subtilis and B. licheniformis. Both T2 and T3 groups exhibited superior values of SOD and CAT compared to other groups ( P < 0.05).
Table 4 shows that the treatment with three levels of B. licheniformis and B. subtilis had a significantly higher effect ( P < 0.05) on Red Tilapia reproductive hormones compared to the control group. Specifically, the probiotic treatment at level 3 (T3, 0.03 g/m 3 ) showed significant results ( P < 0.05) in increasing the concentrations of the hormones FSH, LH, E2, and progesterone compared to the other treatment groups. Regarding testosterone hormone parameters, the highest concentration increase was observed in the T3 treatment, while there was no significant difference among T1, T2, and the control group.
The findings suggest that the levels of B. subtilis and B. licheniformis positively influenced the organosomatic indexes and reproductive functions (Table 5 ). Both B. subtilis and B. licheniformis levels contributed to hepatic and gonadal development in both sexes compared to the control group ( P < 0.05). The hepatosomatic index (HSI) ranged from 3.07 to 3.55% for males and 3.09–3.34% for females. The viscerosomatic index (VSI) was significantly impacted by the addition of various doses of B. subtilis and B. licheniformis in all treatments ( P < 0.05), ranging from 9.99 to 11.06%. However, the VSI for females showed no significant effect with the addition of different levels of B. subtilis and B. licheniformis in all treatments ( P > 0.05). The gonadosomatic index (GSI) significantly improved in all probiotic treatments ( P < 0.05), ranging from 3.36 to 4.95% for males and 4.06–5.05% for females.
The inclusion of varying levels of B. subtilis and B. licheniformis resulted in a notable improvement in egg diameter, the average number of fry (spawning efficiency and larval production), and the average fry weight. Egg diameter varied from 1.17 mm to 1.69 mm, the mean number of fries ranged from 1130 to 1478, and the average fry weight ranged from 16.05 g to 16.89 g, as presented in Table 5 .
The current findings show the expression of genes associated with development and reproduction, including Vasa , nanos1a , nanos2 , dnd1 , pum1 , AMH , and VTG in testicular (Fig. 1 ) and ovarian (Fig. 2 ) tissues of Red Tilapia. It was noted that the expressions of Vasa , nanos1a , nanos2 , dnd1 , pum1 , AMH , and VTG genes in testicular tissues were significantly upregulated in response to different graded levels of B. subtilis and B. licheniformis ( P < 0.05) compared to the control group (Fig. 1 ). Additionally, the expressions of Vasa , nanos1a , nanos2 , dnd1 , pum1 , AMH , and VTG genes in the ovarian tissues followed the same pattern (Fig. 2 ). This upregulation increased in a dose-dependent manner, with levels of 0.03 g/m 3 of B. subtilis and B. licheniformis being the most effective (Figs. 1 and 2 ).
Effect of the B. subtilis and B. licheniformis (T0; 0, T1; 0.01, T2; 0.02, T3; 0.03, g/m 3 ) added to the water on expression of reproduction-associated genes in the testis of Red Tilapia
Effect of the B. subtilis and B. licheniformis (T0; 0, T1; 0.01, T2; 0.02, T3; 0.03, g/m 3 ) added to the water on mRNA of reproduction-related genes in the ovaries of Red Tilapia
Sections of fish testicular tissue from the control group (T0; Fig. 3 A) showed the typical anatomy of interstitial cells (It), spermatocytes (Sp), spermatids (St), spermatozoa (Sz), and testicular lobules (T). The testes treated with B. subtilis and B. licheniformis contained all stages of spermatogenesis. In the T1 group (Fig. 3 B), which received 0.01 g/m 3 of B. subtilis and B. licheniformis , we noticed normal and healthy architectures of seminiferous tubules containing spermatocytes, spermatids, and spermatozoa. There was a noticeable increase in the abundance of spermatogenetic cells and growth of testicular tubules, particularly in both the T2 (0.02 g/m 3 ; Fig. 3 C) and T3 groups (0.03 g/m 3 ; Fig. 3 D) treated with B. subtilis and B. licheniformis . The T3 group showed an increase in spermatogenic cells, particularly spermatids and mature spermatozoa (Fig. 3 D).
Photomicrographs of transverse sections of mature testis of Red Tilapia kept in various levels of B. subtilis and B. licheniformis {0 (Fig. 3 A ), 0.01(Fig. 3 B ), 0.02 (Fig. 3 C ), 0.03 (Fig. 3 D , g/m 3 } added to the water. Interstitial cells (It), spermatocytes (Sp), spermatids (St), spermatozoa (Sz), testicular lobules (T). [H&E stain was used, 100 μm]
The control group (T0) fish ovaries (Fig. 4 A) displayed a slightly normal ovarian structure containing normal chromatin nucleolar oocytes (C), vitellogenic oocytes, cortical alveoli (CA), ripe oocytes (R), yolk globules (Y), and previtellogenic stage (Pr). Fish fed on different levels of B. subtilis and B. licheniformis (0.01, 0.02 and 0.03 mg/m 3 ) exhibited normal development in all types of oocytes, including chromatin nucleolar oocytes (C), previtellogenic stage (Pr), vitellogenic oocytes, cortical alveoli (CA), ripe oocytes (R), yolk globules (Y), postvitellogenic stage (Po), and postspawning ova (PSo) (Fig. 4 B). This development was most pronounced in the T2 (0.02 g/m 3 ) and T3 (0.03 g/m 3 ) groups. Compared to the control group (T0), the T2 (Fig. 4 C) and T3 (Fig. 4 D) groups showed an improvement in oocytes with post-ovulation luteinization and demonstrated superiority in oogonia and oocyte occurrence at various developmental stages.
Photomicrographs of transverse sections of mature ovaries of Red Tilapia kept in water supplemented with various levels of B. subtilis and B. licheniformis {0 (Fig. 4 A ), 0.01 (Fig. 4 B ), 0.02 (Fig. 4 C ), 0.03 (Fig. 4 D ), g/m 3 }. Arrows: stroma that around the vitellogenic oocytes’ follicles, growing oocytes at different developmental stages, normal chromatin nucleolar oocyte (C), vitellogenic oocytes with cortical alveoli (CA), ripe oocytes (R), yolk globules (Y), previtellogenic stage (Pr), postvitellogenic stage (Po), postspawning ova are collapsed (PSo), asterisk: degeneration of some tissues around the oogonia follicles. [H&E stain was used, 100 μm]
Aquaculture has recently played a significant role as a vital food source, supplying humans with excellent protein and easily absorbable minerals, particularly in developing nations such as Egypt [ 20 , 40 , 41 ]. Enhancing fish broodstock reproductive capacity with probiotic supplements can benefit the industry’s sustainability. While most studies focus on probiotics’ role in growth stages, their impact on reproductive capacity is less explored. In this study, we investigated the effects of adding BSL to water on red Tilapia’s reproductive variables. The results show that supplementing water with BSL significantly improved hematobiochemical parameters, reproductive hormones, organosomatic attributes, and reproductive capacity in red Tilapia. Gene expression analysis revealed upregulation of reproductive-related genes in testicular and ovarian tissues in response to varying levels of B. subtilis and B. licheniformis compared to fish on a basal diet. Various reports have documented the positive impacts of different additives on fish. Among these additives, probiotics, especially Bacillus strains, have become the most widely used and popular in aquaculture [ 23 , 42 ]. The production of fish in aquaculture heavily depends on water conditions. To achieve optimal reproductive capacity, survivability, and production, it is crucial to enhance the aquatic environment by reducing aquatic pathogens and improving water quality. This will lead to successful reproduction [ 6 ]. The findings of the current trial demonstrate a noticeable improvement in water quality, supported by a considerable decrease in total hazardous and toxic degrees of ammonia in the probiotics-treated groups, especially the T3 group. Many previous studies have found similar results [ 9 , 43 ].
According to the findings of a research conducted by [ 44 ], the addition of B. licheniformis as denitrifying bacteria to rearing water decreases the levels of toxic components (TAN and NH 3 ) and improves the breakdown of protein and starch in leftover feeds. The quality of water is enhanced by the biodegradation of nitrogenous wastes by Bacillus species, resulting in waste mineralization [ 44 ]. Maintaining good water quality is crucial for the survival of aquatic organisms especially in Broadstock fish, with ammonia nitrogen and nitrite nitrogen being key indicators in aquaculture. High levels of these compounds can be toxic to farmed species. Effective water quality management is essential in aquaculture production. Enriching water with efficient microbial communities can enhance organic matter recycling and maintain a clean water environment for farmed fish [ 45 ]. Previous studies have found that the addition of B. subtilis (10 9 CFU/mL) significantly decreased the total nitrogen and ammonia nitrogen concentrations in water. Additionally, Cha et al. [ 46 ], performed that B. subtilis (0.5% of the diet) effectively reduced the concentration of ammonia nitrogen in the Japanese flounder ( Paralichthys olivaceus ) culture system. The authors suggested that probiotics play a crucial role in water quality by breaking down organic matter and converting NH 4+ to NO 3 . Furthermore, probiotics have been shown to eliminate pathogenic bacteria from water. Improving water quality can enhance fish health, leading to increased production and reduced susceptibility to disease.
Haemato-biochemical parameters are considered valuable indicators for evaluating the health profile of fish [ 47 , 48 ]. According to our findings, the use of B. subtilis and B. licheniformis improved the hematopoietic state of red tilapia. Hematological parameters in the current study, such as HB, mean MHC, MCHC, and HCT in the treated groups with the addition of probiotics also significantly increased compared to the control group, indicating a high capacity for oxygen carrying in the blood [ 49 ]. On the contrary, the MCV was not significantly affected in all treatments. The addition of B . subtilis in water demonstrated a significant improvement in albumin, total protein, and globulin values compared to the control group [ 50 , 51 ]. Glucose levels in our study exhibited a gradual decline in all treated groups, which is in line with the results of a previous study [ 52 ]. The reduction in glucose levels was attributed to the probiotic’s treatment altering the expression of genes involved in glucose uptake and lowering overall glucose levels in zebrafish larvae [ 52 ]. Significant differences were observed in the blood serum composition of red tilapia that received supplementation with B. licheniformis and B. subtilis . Components in the blood serum indicate the physiological performance of the fish body, especially in relation to the functions of vital organs such as the liver, kidneys, and the circulatory system. Hepatic function enzymes, AST, and ALT are biochemical indices of liver function and health. These indicators are used to evaluate how additives can influence the metabolic activities and overall health of fish [ 41 ]. In our trial, a significant reduction in liver activities was observed in all groups treated with B. subtilis and B. licheniformis , which is consistent with findings reported in Nile tilapia showing the same effect of these enzymes when probiotics are added to the rearing water.
The part of probiotics in controlling metabolic enzymes has also been explored and studied in a scarce other aquatic fish species. Studies by [ 53 ] and [ 54 ] suggested that feeding Nile tilapia a diet supplemented with B. subtilis may reduce ALT and AST activities.
In the current research, we noticed a significant decrease in blood levels of creatinine, urea, and uric acid levels showed a significant decrease with the increase in probiotic levels. This data was in contrast to the findings by [ 55 ] and [ 20 ], who indicated that no notable changes in creatinine and urea levels among supplemented groups with probiotics. Additionally, the activities of antioxidants SOD and CAT were increased with the addition of graded levels of B. subtilis and B. licheniformis ( p < 0.05), consistent with the results of study by [ 20 ]. Prebiotics and probiotics have been stated to improve the reproductive capability of certain fish species. For instance, Zebrafish ( Danio rerio ) fed a diet enriched either bacillus spp or lactobacillus spp showed improvements in gonad development, fecundity, egg production, GSI, and the number of viable fries produced [ 56 , 57 ].
As a secondary effect of increased absorption and utilization of nutrients in aquatic animals receiving probiotic supplementation, there is an increased availability of nutrients essential for reproductive system function, including the production of hormones important for reproductive function. Pituitary gonadotropins (GnRH) such as LH and FSH are the main regulators of gametogenesis in teleost fish [ 58 ].
The data of the current experiment is consistent with the findings by [ 27 ], indicating that red tilapia receiving probiotic supplementation will experience an increase in the production of hormones such as testosterone, FSH, LH, estrogen, and progesterone compared to the control group.When using probiotics for aquatic animals, the type of probiotic bacteria and the dosage of probiotics play a significant role in the outcomes. In this study, the T3 treatment group (dose 0.03 g/m 3 ) exhibited a greater increase in hormone concentrations compared to the T2 and T1 treatment groups [ 27 ]. The results of this experiment showed that the treatment with three levels of probiotics containing B. subtilis and B. licheniformis had a significantly greater effect on the reproductive hormones of red tilapia compared to the fish fed the basal diet without any treatment.
Specifically, the probiotic treatment at level 3 (T3) produced highly significant results in increasing the concentration of the hormones FSH, LH, E2, and P compared to the other treatment groups. Regarding testosterone hormone, the highest level was found in the T3 treatment, while for T1 and T2, they did not differ significantly different from the control group (T0).
Studies by several researchers [ 48 , 59 , 60 ] have documented that beneficial microbes can lead organisms utilize energy sources more efficiently, leading to improved growth and reproductive performance in zebrafish [ 61 ]. In our study, the inclusion of levels of B. licheniformis and B. subtilis notably enhanced the growth performance of red tilapia compared to the control group.
Furthermore, higher levels of these probiotics in red tilapia groups reared in water treated with B. subtilis and B. licheniformis can be directly contributed to the improvement of water quality. There was a substantial variation ( P < 0.05) between the treatment groups in the GSI percentage, mean number of fries, and mean fry weight parameters. Only the group receiving probiotic supplementation showed a significant difference in the HIS percentage and egg diameter parameters compared to the control group. Body indices, including GSI, VSI, and HSI, which indicating dietary value, growth, and feed utilization, can be improved by adding feed with a mixture of B. subtilis and B. licheniformis [ 62 ]. Another study of [ 62 ] reported that all doses of probiotics had a substantial valuable consequence on the GSI and HSI indices compared to the control treatment. This suggests that adding B. licheniformis and B. subtilis can boost the reproductive capability of zebrafish [ 56 , 57 ].
Dead-end (dnd) , Nanos , pumilio (pum) , piwil-like (piwil) vasa , and genes are known to be implicated in translational repression of germ cells [ 63 ], which is believed to be essential for the preservation of germline integrity across animal phyla, containing mice [ 64 ], zebrafish [ 65 ], and Xenopus [ 66 ]. Recently, four nanos’ genes [ 67 ], two piwil genes [ 68 ] and three vasa genes [ 69 ] have been identified in tilapias. Additionally, in silico examination of public databases by NCBI revealed anticipated sequences for three pum genes and one dnd1a . Vitellogenin (Vtg) is a reproductive protein found in females, that is broken down into yolk proteins. Lipovitellin (Lv), and phosvitin (Pv), which are deposited in eggs to provide essential nutrients for early-stage embryos. Several studies have confirmed that probiotics can improve the reproductive capacity in Nile tilapia by supporting reproductive-related genes, as observed in this study. A study by [ 70 ] clarified that probiotics (0.5 g/kg) added to Nile tilapia feed during the breeding season improved reproductive performance and profitability.
In the extant work, the transcript of development-reproduction-related genes in red tilapia fed with B. subtilis and B. licemiformis were significantly upregulated compared to fish reared in the control group. This highlights the beneficial effects of B. subtilis and B. licemiformis on fish reproduction, in addition to the previously reported improvements in hematology profile, blood metabolites, and reproductive parameters such as GSI, egg diameter, and fry production. Male zebrafish fed a diet with a containing probiotic P. acidilactici exhibited higher expression of fertility markers ( lepa , dmrt , and bdnf ) compared to the control group [ 71 ]. This indicates that P. acidilactici could be a promising probiotic supplement to enhance molecular parameters in testicular cells of male zebrafish, potentially leading to improve the reproductive performance, sperm quality.Probiotics have been shown to prevent apoptosis and enhance survivability in fish during the growth period [ 72 ]. They also stimulate the intratubular and tubular sections, which are known to enhance sperm production [ 71 ]. Certain probiotics have been shown to activate various cell types, including neuronal, connective tissue, blood/lymphatic vessels, mast cells, macrophages, and steroidogenic Leydig cells. Additionally, probiotic supplementation in feed has been found to improve fish reproductive health and feed utilization, particularly with lactic acid bacteria [ 24 ].
Probiotics have the potential to modulate gene expression patterns or hormone levels that regulate fish reproduction [ 73 ], thereby enhancing reproductive functions and activating reproductive genes to address reproductive disorders when added to the diet or water. Histological investigations revealed that the addition of B. subtilis and B. licemiformis enhanced gonadal development in red tilapia, particularly in spermatogenic cells, including spermatids and mature spermatozoa. Female fish reared in 0.02 and 0.03 g/m 3 showed different stages of oocyte development, with the best gonadal development observed in the 0.03 g/m 3 group, which had a higher number of mature and ripe oocytes. These findings are consistent with those reported by [ 74 ] in Nile tilapia. Further studies are needed to confirm these results, as there is a lack of research on the potential effects of probiotics on reproductive performance in fish species, especially using omics tools.
The study showed that adding B. subtilis and B. licheniformis at a concentration of 0.03 g/m 3 can enhance fish blood profile and reproductive health. This experiment demonstrated that probiotics in water can improve water quality, hematological and biochemical parameters in red tilapia broodfish, and support gonad maturation, gametogenesis production, gene expression, and overall reproductive performance. Additional research is required to validate these findings, as there is a dearth of studies examining the potential impacts of probiotics on reproductive performance in fish species.
No datasets were generated or analysed during the current study.
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Fish Research Centre, Faculty of Agricultural Environmental Sciences, Arish University, El-Arish, 45511, Egypt
El-Sayed Hemdan Eissa
Oceanography Department, Faculty of Science, Alexandria University, Alexandria, Egypt
Abdel-Fattah M. El-Sayed
Department of Husbandry and Development of Animal Wealth, Mansoura University, Mansoura, Egypt
Basma M. Hendam
National Institute of Oceanography and Fisheries (NIOF), Cairo, Egypt
Sara F. Ghanem
Department of Fish Resources and Aquaculture, Faculty of Environmental Agricultural Sciences, Arish University, El-Arish, Egypt
Heba E. Abd Elnabi
Zoology Department, Faculty of Science, Port-Said University, Port Fouad, 42526, Egypt
Yasmin M. Abd El-Aziz
Department of Animal Production, Faculty of Agriculture, Zagazig University, Zagazig, 44511, Egypt
Sameh A. Abdelnour
Biotechnology Department, Fish Farming and Technology Institute, Suez Canal University, Ismailia, 41522, Egypt
Moaheda E.H. Eissa
Department of Aquaculture, Faculty of Fish Resources, Suez University, Suez, 43512, Egypt
Hagar Sedeek Dighiesh
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Increasing functional residual capacity (FRC) or tidal volume (V T ) reduces airway resistance and attenuates the response to bronchoconstrictor stimuli in animals and humans. What is unknown is which one of the above mechanisms is more effective in modulating airway caliber and whether their combination yields additive or synergistic effects. To address this question, we investigated the effects of increased FRC and increased V T in attenuating the bronchoconstriction induced by inhaled methacholine (MCh) in healthy humans.
Nineteen healthy volunteers were challenged with a single-dose of MCh and forced oscillation was used to measure inspiratory resistance at 5 and 19 Hz (R 5 and R 19 ), their difference (R 5-19 ), and reactance at 5 Hz (X 5 ) during spontaneous breathing and during imposed breathing patterns with increased FRC, or V T , or both. Importantly, in our experimental design we held the product of V T and breathing frequency (BF), i.e , minute ventilation (V E ) fixed so as to better isolate the effects of changes in V T alone.
Tripling V T from baseline FRC significantly attenuated the effects of MCh on R 5 , R 19 , R 5-19 and X 5 . Doubling V T while halving BF had insignificant effects. Increasing FRC by either one or two V T significantly attenuated the effects of MCh on R 5, R 19 , R 5-19 and X 5 . Increasing both V T and FRC had additive effects on R 5 , R 19 , R 5-19 and X 5 , but the effect of increasing FRC was more consistent than increasing V T thus suggesting larger bronchodilation. When compared at iso-volume, there were no differences among breathing patterns with the exception of when V T was three times larger than during spontaneous breathing.
These data show that increasing FRC and V T can attenuate induced bronchoconstriction in healthy humans by additive effects that are mainly related to an increase of mean operational lung volume. We suggest that static stretching as with increasing FRC is more effective than tidal stretching at constant V E , possibly through a combination of effects on airway geometry and airway smooth muscle dynamics.
Studies in animals and humans have brought clear evidence that increasing the operating lung volume, i.e., the end-expiratory lung volume above normal functional residual capacity (FRC) or the tidal volume (V T ), reduces airway resistance [ 1 , 2 ] and can attenuate [ 3 ] or reverse [ 4 ] the response to bronchoconstrictor stimuli. These effects of breathing at increased lung volume can be explained by either static or dynamic mechanisms. Since airways and lung parenchyma are interdependent, a static increase of lung volume is associated with an increase of airway caliber by the action of tethering forces opposing both the passive elastic recoil of the airway wall and the active contractile forces of airway smooth muscle. On the other hand, studies in-vitro have shown that dynamic swings can blunt the response of airway smooth muscle to contractile stimuli by mechanisms that reduce its force generation capacity [ 5 , 6 ], though in bronchial segments this effect was observed only when pressure oscillations were raised to twice of those corresponding to normal V T [ 7 ]. In vivo, increasing V T [ 4 ], or breathing frequency (BF), or both [ 8 ] have a bronchodilator effect.
Therefore, it can be expected that increasing FRC or V T, or their combinations, have beneficial effects in counteracting bronchoconstriction in vivo. However, in porcine bronchial segments, static hyper-distension reduced the maximal response to acetylcholine but blunted the relaxant effect of superimposed pressure oscillations of amplitude corresponding to twice the baseline V T [ 9 ], raising the possibility that lung hyperinflation may compete with the bronchodilator effects of increasing V T in vivo. In humans, the relative efficacy of physiologically relevant static hyperinflation and increased dynamic swings in countering airway narrowing has not been studied, but it can be hypothesized that they differ, owing to different underlying mechanisms.
To test this hypothesis, we designed the present study to evaluate whether the bronchodilator effect of breathing at increased lung volumes differs depending on whether attained by increasing FRC or V T . Moreover, we investigated whether the bronchodilator effects of increasing FRC and V T were additive.
Nineteen healthy volunteers (13 males/6 females) with no history respiratory/cardiovascular diseases participated in the study. No one was obese. Main anthropometric and respiratory functional data are reported in Table 1 . Data were collected at Santa Croce and Carle Hospital (Cuneo, Italy), the protocol was approved by the local Ethical Committee, and each subject gave a written informed consent before participation.
Spirometry was measured by a mass flowmeter (SensorMedics Inc., CA, USA) following the ATS/ERS recommendations [ 10 ]. Respiratory impedance was measured by a forced oscillation technique (FOT) as previously described [ 11 , 12 ]. Briefly, sinusoidal pressure oscillations (5 and 19 Hz; ~ 2 cmH 2 O peak-to-peak) were generated by a 16-cm diameter loudspeaker (model CW161N, Ciare, Italy) mounted in a rigid plastic box and connected in parallel to a mesh pneumotachograph and mouthpiece on one side and to a low-resistance high-inertance tube on the other side. Pressure oscillations were applied at the mouth during tidal breathing, while subjects had their cheeks supported by the hands of an investigator to minimize upper airway shunting. The overall load over the tidal breathing frequency range was 0.98 cm H 2 O•L -1 •s. Airway opening pressure and flow were recorded by piezoresistive transducers (DCXL10DS and DCXL01DS Sensortechnics, Germany, respectively) and sampled at 200 Hz. A 15-L/min bias flow of air generated by an air pump (CMP08, 3A Health Care, Italy) was used to reduce dead space to about 35 ml. Pressure and flow signals were processed by a least-square algorithm [ 13 , 14 ] to calculate respiratory resistance at 5 and 19 Hz (R 5 and R 19 , respectively) and reactance at 5 Hz (X 5 ). Artifacts due to glottis closure or expiratory airflow limitation were avoided by discarding breaths showing any of the following features: i) tidal volume <0.1 L or >2.0 L, ii) difference between measured flow oscillation and ideal sine wave with the same Fourier coefficients >0.2 [ 15 ], and iii) ratio of minimum to average X>3.5 [ 11 ]. The same breaths were used to measure V T , breathing frequency (BF), inspiratory and total time of each breath (T I and T Tot , respectively), and estimate inspiratory drive (V T /T I ), inspiratory duty cycle (T I /T Tot ), and minute ventilation (V E ).
Subjects attended the laboratory for spirometry and determination of the dose of methacholine (MCh) to be used for the study day. For this purpose, after baseline FOT measurements, MCh chloride dry-powder (Laboratorio Farmaceutico Lofarma, Milan, Italy) was dissolved in distilled water and administered by an ampoule-dosimeter system (MB3 MEFAR, Brescia, Italy) delivering aerosol particles with a median mass diameter of 1.53-1.61μm, while subjects breathed quietly in a sitting position. The starting dose was of 300 μg followed by doubling doses until R 5 increased by at least 100% from baseline.
Baseline FOT measurements were taken during 2 min of spontaneous tidal breathing. Then, the subjects were trained to breathe, by using visual feed-back of spirometry tracing, for 2 min with imposed combinations of FRC or V T . Thereafter, each subject inhaled a single dose of MCh equal to the last dose given on the pre-study day and R 5 was measured 2 min later during spontaneous tidal breathing to confirm the persistence of bronchoconstriction. Then, FOT measurements were taken while subjects maintained for 2 min each of the following imposed breathing patterns in randomized order (Fig. 1 ): A) spontaneous V T from spontaneous FRC, B) near double V T from spontaneous FRC, C) near triple V T from spontaneous FRC, D) spontaneous V T from FRC increased by 1 V T , E) near double V T from FRC increased by 1 V T , and F) spontaneous V T from FRC increased by 2 V T . For each V T increase the subjects were asked to adjust BF to prevent large increments of V E . Before each change of breathing pattern, R 5 was measured during spontaneous tidal breathing to check for the stability of bronchoconstriction. If R 5 was 10% or more lower than initial post-MCh value an additional half dose of MCh was given to restore bronchoconstriction. This happened occasionally in 6 subjects, with no relation to any specific breathing pattern. At the end of the study, aerosol albuterol was administered to relieve symptoms if any.
Patterns of breathing before after methacholine (MCh) with tidal volume (V T ) initiated from spontaneous or increased functional residual capacity (FRC). For each condition, respiratory impedance measures were calculated over the 3 mid-quintiles of the whole inspiratory phase (upper panel) or over the 3 mid-quintiles of iso-volume inspiratory portions (lower panel) as shown by the thick lines
For each breathing pattern, R 5 , R 19 , R 5-19 , and X 5 were calculated over the 3 mid-quintiles of the whole inspiratory phase (Fig. 1 , upper panel) or over the 3 mid-quintiles of iso-volume inspiratory portions (Fig. 1 , lower panel).
Differences in R 5 , R 19 , R 5-19 , X 5 , V T , BF, V T /T I , T I /T Tot , and V E between conditions were tested for statistical significance by a one-way repeated-measure analysis of variance (ANOVA) with Holm-Sidak post-hoc test for multiple-comparisons. Values of p<0.05 were considered statistically significant. Data are presented as mean ± standard deviation (SD).
The spontaneous breathing pattern after MCh (A) did not differ significantly from the spontaneous pattern before methacholine (Table 2 ). V T and BF changed with the imposed patterns (B-F) as per protocol. Even though great attention was paid to maintain V E as constant as possible among the imposed breathing patterns, it was with patterns C, E, and F that V E slightly but significantly increased than with patterns than A and B. These differences were associated with significant differences in mean inspiratory, V T /T I . Neither V E nor V T /T I were significantly different among breathing patters C, D, E, and F . There were no significant differences in T I /T TOT among all breathing patterns.
In general, breathing at increased FRC, increased V T , or both attenuated the changes induced by MCh inhalation on R 5 , R 19 , R 5-19 , and X 5 (Fig. 2 and Supplemental Table 1).
Effects of increasing tidal volume from spontaneous functional residual capacity (patterns A , B , C ) ( A ), increasing functional residual capacity with spontaneous (patterns A , D , F ) ( B ), or both (patterns B , E ) ( C ) on mid-inspiration impedance measures. Effects of patterns achieving the same peak volume ( C vs. E and vs. F ) on mean-inspiratory impedance measurements ( D ). V T , tidal volume; FRC, functional residual capacity. R 5 , respiratory resistance at 5 Hz, R 19 , respiratory resistance at 19 Hz; R 5-19 , difference in respiratory resistance between 5 and 19 Hz; X 5 , respiratory reactance at 5 Hz. Columns heights indicate means and error bars standard deviations. *, p <0.005; **, p <0.01; p <0.001
Increasing V T from spontaneous FRC was associated with significant reductions of R 5 , R 19 , R 5-19 and less negative X 5 when V T was tripled ( pattern C ) but not doubled ( pattern B ) compared to spontaneous breathing ( pattern A ) V T . Yet, the attenuating effects of pattern C were significantly greater than those of pattern B .
Increasing FRC by either one ( pattern D ) or two ( pattern F ) V T with constant spontaneous V T was associated with significant reductions of R 5 and R 19 than pattern A, while R 5-19 was significantly reduced and X 5 less negative with pattern F but not pattern D .
Increasing both V T and FRC ( pattern E ) was associated with significantly lower R 5 , R 19 , R 5-19 and less negative X 5 than increasing V T alone ( pattern B ) and significantly lower R 19 than increasing FRC alone ( pattern D ).
Breathing patterns with the same peak volume, no matter whether achieved by increasing V T or FRC or both ( patterns B vs. D and C vs. E and vs. F ) showed insignificantly different effects on airway narrowing.
Notably, R 5 (cmH 2 O•L -1 •s) was reduced by 0.57±1.18 when V T was doubled ( pattern B vs pattern A), by 1.19±0.70 when FRC was increased by 1 V T ( pattern D vs pattern A ), and by 1.84±0.88 when both V T and FRC were increased ( pattern E vs pattern A ). Similarly, R 19 (cmH 2 O•L -1 •s) was reduced by 0.29±0.35 when V T was doubled ( pattern B vs pattern A) , by 0.48±0.46 when FRC was increased by 1 V T ( pattern D vs pattern A ), and by 0.91±0.42 when both V T and FRC were increased ( pattern E vs pattern A ). These results suggest simply additive effects, but the increase of FRC was more potent to mitigate airway narrowing than the increase in V T .
In general, R 5 , R 19 , and R 5-19 were inversely related to the lung volume at which they were measured (Fig. 3 and Supplemental Table 2), while the X 5 values were inconsistently related to lung volumes.
Effects of increasing tidal volume from spontaneous (patterns A , B , C ) or increased (patterns D , E , F ) functional residual capacity on iso-volume inspiratory impedance measures. Other abbreviations as in Fig. 2 . Columns heights indicate means and error bars standard deviations. *, p <0.005; **, p <0.01
At low iso-volume, R 5 and R 19 , were significantly lower and X 5 was less negative than during spontaneous breathing ( pattern A ) when V T was tripled ( pattern C ) but not doubled ( pattern B ). Yet, the attenuating effects of pattern C on R 5 and X 5 were significantly greater than those of pattern B .
At mid iso-volume, R 5 , R 19 , and R 5-19 did not differ significantly with increments of V T ( patterns B and C) , or FRC ( pattern D ), or both ( pattern E ). However, X 5 was significantly less negative when both FRC and V T were increased ( pattern E ) than when V T ( pattern B ) or FRC ( pattern D ) were increased alone.
At high iso-volume, there were no significant differences with increments of V T ( pattern C ), or FRC ( panel F ), or both ( panel E ).
The main findings of the present study in healthy volunteers were that 1) the changes of respiratory impedance induced by inhaled MCh were significantly attenuated by increasing FRC, or V T , or both, 2) increasing FRC had more consistent effects than increasing V T , 3) the effects of increasing FRC and V T were additive, and ) volume-independent effects attributable to tidal stretching were observed only when V T was three times larger than during spontaneous breathing.
We used oscillometry because it is the only available method enabling intra-breath measurements of respiratory mechanics over specific portions of lung volume during tidal breathing, but it has two major limitations. First, oscillometry does not directly measure airway resistance but also lung tissue and chest wall resistances. Airway resistance is inversely related to V T whereas lung tissue resistance is inversely related to BF [ 2 ]. Therefore, it is possible that the effects of increasing V T on airway caliber were counteracted by the effects of decreasing BF on tissue resistance. We think this had no major effect on our results because the attenuation of R 5 , which reflects in large part tissue resistance, was not less than the attenuation of R 19 , which mainly reflect airway resistance. Second, breathing at increased lung volumes requires activation of inspiratory muscles, which increases chest wall elastance [ 16 ]. Therefore, we cannot exclude that changes in X 5 with different breathing patterns were counteracted by changes in chest wall stiffness.
Although our subjects were asked to maintain V E as constant as possible by decreasing BF when V T was increased, there was a tendency for V E to increase (Table 2 ), thus likely resulting in an increased alveolar ventilation and airway hypocapnia, mainly when achieved by increasing V T . Hypocapnia has a bronchoconstrictor effect [ 17 ], thus possibly counteracting the bronchodilator effects of imposed breathing patterns. We did not measure end-tidal CO 2 , but we believe this had no major impact on our results for two reasons. First, assuming normal anatomical plus instrumental dead space and CO 2 production, we estimated a mean difference in alveolar PCO 2 between patterns C and A to be approximately 7 mmHg, which was reported to have insignificant effects on the respiratory impedance of healthy subjects [ 18 ]. Second, the differences in V E between any imposed patters were insignificant and differences in alveolar PCO 2 presumably minimal.
Finally, for changes in V T were associated with changes in BF and the ratio T I /T TOT remained constant, the effects of tissue viscoelasticity could not be evaluated. Nevertheless, breathing patterns with low BF would have increased the time for airway smooth muscle relaxation during the inspiratory phase but also for re-shortening during the expiratory phase.
The present study was designed on the premises that both lung hyperinflation and increased breathing depth are mechanisms protecting against airway narrowing, but their relative efficacies are unknown.
That increasing lung volume is associated with a proportional increase of airway conductance, i.e., the reciprocal of airway resistance, was first reported in 1958 by Briscoe and Dubois [ 1 ] and subsequently confirmed in excised animal [ 19 ] and human [ 20 ] lungs with relaxed airways. This effect was simply attributed to a geometric change of airways being distended by the static radial traction of the surrounding lung parenchyma. Studies in contracted airway smooth muscle strips have consistently shown that sustained step-changes of length can rapidly attenuate active tension, possibly due to disassembly of the contractile apparatus, followed by a gradual recovery due to length adaptation [ 20 , 21 ]. By contrast, in whole bronchial segments a sustained inflationary increase of transmural pressure also caused an immediate reduction in tension, but this was followed by a continuous gradual decrease [ 22 ]. Airway wall stiffening was proposed to explain the difference between intact bronchi and muscle strips [ 22 , 23 ]. In our study, R 5 was stable or decreased between the different breathing patterns, but never increased, which makes the occurrence of length adaptation unlikely. Thus, it is possible that the attenuations of airway narrowing we observed after 2 min of breathing at increased FRC reflected not only geometric changes in airway caliber but also mechanisms opposing both the passive elastic recoil of the airway wall and the active contractile forces of airway smooth muscle.
The inhibitory effect of cycling stretching on airway smooth muscle active force generation has been reported consistently in both isolated muscle strips [ 5 , 6 ] and isolated bronchial segments [ 7 ]. It is well-established in animals [ 7 ] and humans [ 4 , 24 ] that the magnitude of the bronchodilator effects of tidal breathing increases with increasing frequency of breathing and with increasing tidal volume. Two independent lines of evidence suggest, further, that the attenuation of smooth muscle contractile force is attributable to changes of V E , which is the product V T x BF, independently of changes of either V T or BF taken individually [ 24 , 25 ]. Equivalently, neither the amplitude of tissue cyclic strain nor the cyclic frequency is as important as their product, namely, the amplitude of the tissue strain rate. To assess this phenomenon still further, in this report we used an experimental design in which we held the product V T x BF fixed so as to better isolate the effects of changes in V T alone. This is an important issue in our study, as we see that when V E could not be kept constant ( pattern C vs A ) the impedance values at low iso-volume were significantly attenuated presumably because of the higher mean inspiratory flow (V T /T I ) causing a faster lung stretching rate rather than the increase in V T itself.
Three theories can be invoked to explain the above findings [ 26 ], namely, that stretching of airway smooth muscle causes a plastic rearrangement of the contractile apparatus [ 6 , 27 , 28 ], or modifies the crossbridge cycling rate and latch bridges formation [ 5 ] or causes temporary detachment of attached cross bridges [ 29 ].
In an attempt to examine the relative bronchodilator effects of static hyperinflation and dynamic stretching, we measured inspiratory impedance in healthy subjects with MCh-induced bronchoconstriction breathing with different combinations of FRC and V T . As expected, increasing either V T or FRC significantly attenuated the changes induced by MCh on R 5 and R 19 , R 5-19 , suggestive of a generalized increase of airway caliber, but also decreased R 5-19 and made X 5 less negative. To the extent that an increase in R 5-19 and a decrease in X 5 reflect heterogeneous distribution of time constants within the lung periphery [ 30 ], the significant improvement of these variables with the increase in FRC and V T (Figs. 2 and 3 ) suggests that increasing lung volumes no matter how it was achieved made ventilation more homogeneous. While the effects of increasing V T on R 5 and R 19 were significant only when it was threefold the spontaneous V T , the effects of increasing FRC where already significant when it was increased by one V T , suggesting a more consistent effect of increasing static than dynamic tidal stretching.
The effects of increasing both V T and FRC were additive, i.e. , the effect of dynamic stretching was not blunted by an increased static stretch. This finding is in apparent contradiction with a study showing that in isolated bronchial segments hyperinflation blunted the effect of pressure oscillations corresponding to twice a normal V T [ 9 ] In that study, bronchi were hyperinflated at a transmural pressure of 20 cmH 2 O, where airway compliance is reduced [ 7 ] and so are the amplitude of volume oscillation and airway smooth muscle strain. Examining our data in the light of a previous study [ 31 ], (Fig. 3 ), we estimate that the largest end-tidal inspiratory volumes achieved as with patterns C, E and F would have not exceed the values associated with transpulmonary pressures in excess of 20 cm H 2 O. Since bronchial transmural pressure might differ from transpulmonary pressure in the presence of bronchoconstriction [ 32 ], we cannot exclude that stress on airway walls increased with the increase of end-inspiratory volume. Therefore, the increments of V T in our study were likely to reflect increments of airway smooth muscle strain but not stress. The latter, however, does not seem to be the major determinant of the decrease in airway smooth muscle contractility with breathing maneuvers [ 33 , 34 ].
The fact that the effects of FRC and V T were simply additive does suggest that lung hyperinflation and tidal swings operated via a similar mechanism, viz. increase of operational lung volume. This interpretation is supported by the lack of differences at iso-volumes among most breathing patterns. The only exceptions were the lower R 5 , R 19 , R 5-19 , and less negative X 5 at low lung volume after triple V T and the less negative X 5 at mid lung volume with breathing patterns with the highest end-inspiratory lung volume, i.e. , tripling V T ( pattern C ) and doubling V T from increased FRC ( pattern E ). These findings are consistent with a study in airway segments showing modest dilator effects with peak-to-peak pressure oscillations of 10 but not 5 cmH 2 O [ 7 ]. As FOT measurement were taken during the inspiratory phase, these findings possibly reflect volume-independent dynamic effects on airway smooth muscle persisting after the expiratory phase, even when BF and, in turn, expiratory time for re-narrowing was the largest ( pattern C ).
Why was hyperinflation more potent than tidal swings against airway narrowing in the present study is a matter of speculation. Increasing either FRC or V T results in increased mean operational lung volume, which is associates with an increase of airway caliber owing to the tethering force of lung parenchyma opposing the passive elastic recoil of airway walls. However, the mechanisms of static and dynamic stretching on airway smooth muscle active force may be different. One possibility is that in our study the sustained increments of operational lung volume maintained the airway smooth muscle in a condition of reduced force generation capacity by disassembling the contractile apparatus before the occurrence of length adaptation [ 20 , 21 ] or substantial reduction of tethering force due to stress relation of lung parenchyma [ 35 ]. By contrast, additional time-dependent effects of tidal stretching, e.g. , on cross-bridge cycling rate, were possibly obscured by the re-constriction during expiratory phase unless started from very high end-inspiratory volume. Another possible mechanism explaining the larger bronchodilator effects yielded by the increase in FRC rather than V T could be the larger amount of nitric oxide penetrating the airway lumen when narrowing is relieved by distending lung parenchyma [ 36 ].
The results of the present study in healthy subjects cannot be directly extrapolated to asthma because the mechanisms regulating airway smooth muscle contractility and heterogeneity of ventilation may differ in disease. Yet, it is known that FRC increases in asthma with the occurrence of expiratory flow limitation [ 37 ] and decreases after bronchodilator treatments [ 38 ]. Moreover, some beneficial effects of continuous positive airway pressure against airway responsiveness have been reported. To what extent hyperinflation can alleviate asthma symptoms remains to be elucidated, considering that above a given threshold it may cause an increase of inspiratory work of breathing [ 39 ] and limit the increase in V T [ 21 ].
In conclusion, this study provides evidence that both lung hyperinflation and increased tidal stretching yield substantial bronchodilatation in human lungs exposed to a constrictor agent, though the former seems more effective than the latter presumably because of additive effects on airway smooth muscle contractile force and non-contractile airway tissues.
The data that support the findings of this study are available from the authors and are available upon request.
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Dipartimento di Elettronica, Informazione e Bioingegneria, Politecnico di Milano, Milano, 20133, Italy
Alessandro Gobbi & Raffaele Dellaca
Restech Srl, Milano, 20124, Italy
Alessandro Gobbi
Allergologia e Fisiopatologia Respiratoria, ASO S. Croce e Carle, 12100, Cuneo, Italy
Andrea Antonelli
Casa di Cura del Policlinico, Dipartimento di Scienze Neuroriabilitative, Milano, Italy
Giulia M. Pellegrino
Centro Medico Pneumologico Torino, 10129, Torino, Italy
Riccardo Pellegrino
Harvard T. H. Chan School of Public Health, Harvard University, Boston, MA, 02115, USA
Jeffrey J. Fredberg
Department of Medicine, University of Chicago, Chicago, IL, USA
Julian Solway
Dipartimento di Medicina Sperimentale, Università di Genova, 16132, Genova, Italy
Vito Brusasco
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A.G., R.P., J.J.F., J.S. and V.B. wrote the main manuscript text, A.G., R.P. and V.B. conducted statistical analyses and prepared figures and tables. A.A., R.P. and G.P. conducted experimental studies. All authors reviewed the manuscript.
Correspondence to Raffaele Dellaca .
Ethics approval and consent to participate.
The study has been approved by the S. Croce and Carle Hospital Ethics Committee, approval no. 40/13 of 19 th April 2013. The study was conducted in accordance with the Declaration of Helsinki.
Not applicable.
A.G. and R.D. are co-founders and serve as board members of RESTECH Srl, a company that designs, manufactures and sells devices for lung function testing based on Forced Oscillation Technique (FOT). R.D. also reports grants and other from RESTECH, personal fees from Philips Healthcare, outside the submitted work; In addition, R.D. has a patent on the detection of EFL by FOT with royalties paid to Philips Respironics and RESTECH Srl, a patent on monitoring lung volume recruitment by FOT with royalties paid to Vyaire, and a patent on early detection of exacerbations by home monitoring of FOT with royalties paid to RESTECH Srl. A.A., R.P., G.M. P., J.J.F., J.S, and VB have no conflict of interest related to the content of this manuscript.
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Gobbi, A., Antonelli, A., Dellaca, R. et al. Effects of increasing tidal volume and end-expiratory lung volume on induced bronchoconstriction in healthy humans. Respir Res 25 , 298 (2024). https://doi.org/10.1186/s12931-024-02909-9
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Performance evaluation of recursive mean filter using scilab, matlab, and mpi (message passing interface) †.
2. materials and methods, 2.1. recursive mean filter, 2.2. implementations of the rmf, 2.2.1. rmf’s implementation in scilab, 2.2.2. rmf’s implementation in matlab, 2.2.3. rmf’s implementation with c and mpi, 2.3. experimental settings, 3. results and discussion, 4. conclusions, author contributions, institutional review board statement, informed consent statement, data availability statement, conflicts of interest.
Click here to enlarge figure
Image | Small Images | Big Images | ||
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Resolution [pixels] | Size [kb] | Resolution [pixels] | Size [kb] | |
1 | 364 × 239 | 255 | 3641 × 2393 | 25,529 |
2 | 396 × 282 | 328 | 3961 × 2825 | 32,786 |
3 | 450 × 312 | 412 | 4281 × 2977 | 37,341 |
4 | 340 × 510 | 509 | 3200 × 4800 | 45,001 |
5 | 400 × 600 | 704 | 4000 × 6000 | 70,313 |
Name | CPU | Cores | Memory | OS |
---|---|---|---|---|
(PC1) Lenovo IdeaPad Gaming 3 | Intel(R) Core(TM) i5-11320H CPU @ 3.20GHz 3.20 GHz, 11th GEN | 8 | 8 GB | Windows 10 Pro, 64 bits |
(PC2) Dell Inspiron N5110 | Intel(R) Core(TM) i7-2670QM CPU @ 2.20GHz 2.20 GHz | 8 | 8 GB | Windows 10 Pro, 64 bits |
Name | Description | RMF in Scilab | RMF in MATLAB | RMF in C within MPI |
---|---|---|---|---|
t1 | Time for filtering excluding operations read/write files | tic() toc() | tic() toc() | MPI_Wtime() |
t2 | Time for filtering including operations with files | tic() toc() | tic() toc() | MPI_Wtime() |
t3 | Total time for the execution of processes for filtering one image | - | - | time() |
total | Total time for filtering one dataset of images | tic() toc() | tic() toc() | time() |
MATLAB | C with MPI (1 Process) | ||||||
---|---|---|---|---|---|---|---|
3 × 3 | 5 × 5 | 7 × 7 | 3 × 3 | 5 × 5 | 7 × 7 | ||
PC1 | Avg. t1 [s] | 5.86 | 13.10 | 23.63 | 0.55 | 1.25 | 2.36 |
Avg. t2 [s] | 6.12 | 13.36 | 23.89 | 2.44 | 3.14 | 4.26 | |
PC2 | Avg. t1 [s] | 13.37 | 22.03 | 38.14 | 1.11 | 2.24 | 3.93 |
Avg. t2 [s] | 14.12 | 22.76 | 38.85 | 6.62 | 7.78 | 9.48 |
Mask Size | MATLAB | Scilab | C with MPI | ||||
---|---|---|---|---|---|---|---|
1 Process | 2 Processes | 4 Processes | 8 Processes | ||||
PC1 | 3 × 3 | 0.33 | 2235.50 | 1.03 | 1.01 | 1.08 | 1.24 |
5 × 5 | 0.70 | 2286.45 | 1.06 | 1.04 | 1.10 | 1.26 | |
7 × 7 | 1.22 | 2391.15 | 1.14 | 1.11 | 1.14 | 1.29 | |
PC2 | 3 × 3 | 0.68 | 4647.07 | 2.59 | 2.50 | 2.58 | 2.84 |
5 × 5 | 1.26 | 4766.00 | 2.83 | 2.75 | 2.78 | 3.01 | |
7 × 7 | 2.08 | 4952.17 | 3.13 | 2.93 | 3.00 | 3.21 |
Mask Size | MATLAB | C with MPI | ||||
---|---|---|---|---|---|---|
1 Process | 2 Processes | 4 Processes | 8 Processes | |||
PC1 | 3 × 3 | 30.61 | 13.13 | 11.88 | 11.46 | 11.43 |
5 × 5 | 66.82 | 16.61 | 13.67 | 12.67 | 12.39 | |
7 × 7 | 119.44 | 22.22 | 16.54 | 14.50 | 13.64 | |
PC2 | 3 × 3 | 70.58 | 35.90 | 33.35 | 32.34 | 32.19 |
5 × 5 | 113.79 | 41.81 | 36.40 | 33.70 | 33.86 | |
7 × 7 | 194.23 | 50.44 | 41.17 | 36.36 | 36.23 |
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Andreeva, H.; Bosakova-Ardenska, A. Performance Evaluation of Recursive Mean Filter Using Scilab, MATLAB, and MPI (Message Passing Interface). Eng. Proc. 2024 , 70 , 33. https://doi.org/10.3390/engproc2024070033
Andreeva H, Bosakova-Ardenska A. Performance Evaluation of Recursive Mean Filter Using Scilab, MATLAB, and MPI (Message Passing Interface). Engineering Proceedings . 2024; 70(1):33. https://doi.org/10.3390/engproc2024070033
Andreeva, Hristina, and Atanaska Bosakova-Ardenska. 2024. "Performance Evaluation of Recursive Mean Filter Using Scilab, MATLAB, and MPI (Message Passing Interface)" Engineering Proceedings 70, no. 1: 33. https://doi.org/10.3390/engproc2024070033
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Nuclear Energy Revival:
The world’s second-largest economy is expected to leapfrog France and the US as the top source of atomic power.
Within sight of mango and pineapple fields on the Chinese holiday island of Hainan, workers at Linglong One are finishing what will become the world’s first small modular nuclear reactor built for commercial purposes. It’s part of a national fleet of atom-splitting plants that aim to wean the country off coal and imported fuel.
“There are probably not more than seven countries that have the capability to design, manufacture and operate nuclear power plants,” Cui Jianchun, the Chinese foreign ministry’s envoy in nearby Hong Kong, said during an official visit to the plant. “We used to be a follower, but now China is a leader.”
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The classic experimental design definition is: "The methods used to collect data in experimental studies.". There are three primary types of experimental design: The way you classify research subjects based on conditions or groups determines the type of research design you should use. 01. Pre-Experimental Design.
The three main types of experimental research design are: 1. Pre-experimental research. A pre-experimental research study is an observational approach to performing an experiment. It's the most basic style of experimental research. Free experimental research can occur in one of these design structures: One-shot case study research design: In ...
Step 1: Define your variables. You should begin with a specific research question. We will work with two research question examples, one from health sciences and one from ecology: Example question 1: Phone use and sleep. You want to know how phone use before bedtime affects sleep patterns.
Experimental research is a systematic and scientific approach in which the researcher manipulates one or more independent variables and observes the effect on a dependent variable while controlling for extraneous variables. This method allows for the establishment of cause-and-effect relationships between variables.
There are three types of experiments you need to know: 1. Lab Experiment. A laboratory experiment in psychology is a research method in which the experimenter manipulates one or more independent variables and measures the effects on the dependent variable under controlled conditions. A laboratory experiment is conducted under highly controlled ...
Experimental research is best suited for explanatory research—rather than for descriptive or exploratory research—where the goal of the study is to examine cause-effect relationships. ... Regression threat—also called a regression to the mean—refers to the statistical tendency of a group's overall performance to regress toward the ...
An experimental design is a detailed plan for collecting and using data to identify causal relationships. Through careful planning, the design of experiments allows your data collection efforts to have a reasonable chance of detecting effects and testing hypotheses that answer your research questions. An experiment is a data collection ...
Experimental research is the most familiar type of research design for individuals in the physical sciences and a host of other fields. This is mainly because experimental research is a classical scientific experiment, similar to those performed in high school science classes. ... Response vs Explanatory Variables: Definition & Examples. In ...
Experimental science is the queen of sciences and the goal of all speculation. Roger Bacon (1214-1294) Experiments are part of the scientific method that helps to decide the fate of two or more competing hypotheses or explanations on a phenomenon. The term 'experiment' arises from Latin, Experiri, which means, 'to try'.
Experimental research serves as a fundamental scientific method aimed at unraveling. cause-and-effect relationships between variables across various disciplines. This. paper delineates the key ...
Experimental research design is a framework of protocols and procedures created to conduct experimental research with a scientific approach using two sets of variables. Herein, the first set of variables acts as a constant, used to measure the differences of the second set. The best example of experimental research methods is quantitative research.
An example of experimental research in marketing: The ideal goal of a marketing product, advertisement, or campaign is to attract attention and create positive emotions in the target audience. Marketers can focus on different elements in different campaigns, change the packaging/outline, and have a different approach.
Experimental research is commonly used in sciences such as sociology and psychology, physics, chemistry, biology and medicine etc. It is a collection of research designs which use manipulation and controlled testing to understand causal processes. Generally, one or more variables are manipulated to determine their effect on a dependent variable.
Collect the data by using suitable data collection according to your experiment's requirement, such as observations, case studies , surveys , interviews, questionnaires, etc. Analyse the obtained information. Step 8. Present and Conclude the Findings of the Study. Write the report of your research.
Experimental Design. Experimental design is a process of planning and conducting scientific experiments to investigate a hypothesis or research question. It involves carefully designing an experiment that can test the hypothesis, and controlling for other variables that may influence the results. Experimental design typically includes ...
Three types of experimental designs are commonly used: 1. Independent Measures. Independent measures design, also known as between-groups, is an experimental design where different participants are used in each condition of the independent variable. This means that each condition of the experiment includes a different group of participants.
In this case, quasi-experimental research involves using intact groups in an experiment, rather than assigning individuals at random to research conditions. (some researchers define this latter situation differently. For our course, we will allow this definition). In causal comparative (ex post facto) research, the groups are already formed. It ...
Experimental research is widely implemented in education, psychology, social sciences and physical sciences. Experimental research is based on observation, calculation, comparison and logic. Researchers collect quantitative data and perform statistical analyses of two sets of variables. This method collects necessary data to focus on facts and ...
An experiment is a procedure carried out to support or refute a hypothesis, or determine the efficacy or likelihood of something previously untried. Experiments provide insight into cause-and-effect by demonstrating what outcome occurs when a particular factor is manipulated. Experiments vary greatly in goal and scale but always rely on repeatable procedure and logical analysis of the results.
Experimental research design is centrally concerned with constructing research that is high in causal (internal) validity. Randomized experimental designs provide the highest levels of causal validity. Quasi-experimental designs have a number of potential threats to their causal validity. Yet, new quasi-experimental designs adopted from fields ...
You can also create a mixed methods research design that has elements of both. Descriptive research vs experimental research. Descriptive research gathers data without controlling any variables, while experimental research manipulates and controls variables to determine cause and effect.
Study, experimental, or research design is the backbone of good research. It directs the experiment by orchestrating data collection, defines the statistical analysis of the resultant data, and guides the interpretation of the results. When properly described in the written report of the experiment, it serves as a road map to readers, 1 helping ...
Research methods are specific procedures for collecting and analyzing data. Developing your research methods is an integral part of your research design. When planning your methods, there are two key decisions you will make. First, decide how you will collect data. Your methods depend on what type of data you need to answer your research question:
FIELD EXPERIMENT definition: 1. a scientific test that takes place in the real world, and not in a laboratory (= a room or…. Learn more.
We support diverse research activities with talented staff, state-of-the-art facilities and core competencies. From internal collaboration to external partnerships, we work together to advance scientific discovery. ... The significance of symmetry in ICF experiments, Ralph said, is like trying to fly an airplane with a heavy left wing. The ...
Probiotics are becoming increasingly popular as eco-friendly alternatives in aquaculture. However, there is limited research on their impacts on the reproductive efficiency of Red Tilapia (Oreochromis niloticus x O. mossambicus) broodstock. Therefore, this experiment aimed to explore the combined effects of selective probiotics Bacillus subtilis and B. licheniformis (BSL; 1:1) added to water ...
Breathing patterns during the experimental conditions. The spontaneous breathing pattern after MCh (A) did not differ significantly from the spontaneous pattern before methacholine (Table 2).V T and BF changed with the imposed patterns (B-F) as per protocol. Even though great attention was paid to maintain V E as constant as possible among the imposed breathing patterns, it was with patterns C ...
Minnesota's policies around abortion make it among the most protective states for abortion access, according to the Guttmacher Institute, a research and policy organization that supports ...
As a popular linear filter, the mean filter is widely used in different applications as a basic tool for image enhancement. Its main purpose is to reduce the noise in an image and thus to prepare the picture for other image-processing operations depending on the current task. In the last decade, the amount of data, particularly images, that has to be processed in a variety of applications has ...
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