uttered)
The “discussion” section is intended to explain to your reader what your data can be interpreted to mean. As with all science, the goal for your report is simply to provide evidence that something might be true or untrue—not to prove it unequivocally. The following questions should be addressed in your “discussion” section:
Hogg, Alan. "Tutoring Scientific Writing." Sweetland Center for Writing. University of Michigan, Ann Arbor. 3/15/2011. Lecture.
Swan, Judith A, and George D. Gopen. "The Science of Scientific Writing." American Scientist . 78. (1990): 550-558. Print.
"Scientific Reports." The Writing Center . University of North Carolina, n.d. Web. 5 May 2011. http://www.unc.edu/depts/wcweb/handouts/lab_report_complete.html
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Saul McLeod, PhD., is a qualified psychology teacher with over 18 years of experience in further and higher education. He has been published in peer-reviewed journals, including the Journal of Clinical Psychology.
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The experimental method involves the manipulation of variables to establish cause-and-effect relationships. The key features are controlled methods and the random allocation of participants into controlled and experimental groups .
An experiment is an investigation in which a hypothesis is scientifically tested. An independent variable (the cause) is manipulated in an experiment, and the dependent variable (the effect) is measured; any extraneous variables are controlled.
An advantage is that experiments should be objective. The researcher’s views and opinions should not affect a study’s results. This is good as it makes the data more valid and less biased.
There are three types of experiments you need to know:
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 conditions (not necessarily a laboratory) where accurate measurements are possible.
The researcher uses a standardized procedure to determine where the experiment will take place, at what time, with which participants, and in what circumstances.
Participants are randomly allocated to each independent variable group.
Examples are Milgram’s experiment on obedience and Loftus and Palmer’s car crash study .
A field experiment is a research method in psychology that takes place in a natural, real-world setting. It is similar to a laboratory experiment in that the experimenter manipulates one or more independent variables and measures the effects on the dependent variable.
However, in a field experiment, the participants are unaware they are being studied, and the experimenter has less control over the extraneous variables .
Field experiments are often used to study social phenomena, such as altruism, obedience, and persuasion. They are also used to test the effectiveness of interventions in real-world settings, such as educational programs and public health campaigns.
An example is Holfing’s hospital study on obedience .
A natural experiment in psychology is a research method in which the experimenter observes the effects of a naturally occurring event or situation on the dependent variable without manipulating any variables.
Natural experiments are conducted in the day (i.e., real life) environment of the participants, but here, the experimenter has no control over the independent variable as it occurs naturally in real life.
Natural experiments are often used to study psychological phenomena that would be difficult or unethical to study in a laboratory setting, such as the effects of natural disasters, policy changes, or social movements.
For example, Hodges and Tizard’s attachment research (1989) compared the long-term development of children who have been adopted, fostered, or returned to their mothers with a control group of children who had spent all their lives in their biological families.
Here is a fictional example of a natural experiment in psychology:
Researchers might compare academic achievement rates among students born before and after a major policy change that increased funding for education.
In this case, the independent variable is the timing of the policy change, and the dependent variable is academic achievement. The researchers would not be able to manipulate the independent variable, but they could observe its effects on the dependent variable.
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. EVs 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 participating 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.
Lab objectives.
At the conclusion of the lab, the student should be able to:
Hydrogen peroxide is a toxic product of many chemical reactions that occur in living things. Although it is produced in small amounts, living things must detoxify this compound and break down hydrogen peroxide into water and oxygen, two non-harmful molecules. The organelle responsible for destroying hydrogen peroxide is the peroxisome using the enzyme catalase. Both plants and animals have peroxisomes with catalase. The catalase sample for today’s lab will be from a potato.
Enzymes speed the rate of chemical reactions. A catalyst is a chemical involved in, but not consumed in, a chemical reaction. Enzymes are proteins that catalyze biochemical reactions by lowering the activation energy necessary to break the chemical bonds in reactants and form new chemical bonds in the products. Catalysts bring reactants closer together in the appropriate orientation and weaken bonds, increasing the reaction rate. Without enzymes, chemical reactions would occur too slowly to sustain life.
The functionality of an enzyme is determined by the shape of the enzyme. The area in which bonds of the reactant(s) are broken is known as the active site. The reactants of enzyme catalyzed reactions are called substrates. The active site of an enzyme recognizes, confines, and orients the substrate in a particular direction.
Enzymes are substrate specific, meaning that they catalyze only specific reactions. For example, proteases (enzymes that break peptide bonds in proteins) will not work on starch (which is broken down by the enzyme amylase). Notice that both of these enzymes end in the suffix -ase. This suffix indicates that a molecule is an enzyme.
Environmental factors may affect the ability of enzymes to function. You will design a set of experiments to examine the effects of temperature, pH, and substrate concentration on the ability of enzymes to catalyze chemical reactions. In particular, you will be examining the effects of these environmental factors on the ability of catalase to convert H 2 O 2 into H 2 O and O 2 .
As scientists, biologists apply the scientific method. Science is not simply a list of facts, but is an approach to understanding the world around us. It is use of the scientific method that differentiates science from other fields of study that attempt to improve our understanding of the world.
The scientific method is a systematic approach to problem solving. Although some argue that there is not one single scientific method, but a variety of methods; each of these approaches, whether explicit or not, tend to incorporate a few fundamental steps: observing, questioning, hypothesizing, predicting, testing, and interpreting results of the test. Sometimes the distinction between these steps is not always clear. This is particularly the case with hypotheses and predictions. But for our purposes, we will differentiate each of these steps in our applications of the scientific method.
You are already familiar with the steps of the scientific method from previous lab experiences. You will need to use your scientific method knowledge in today’s lab in creating hypotheses for each experiment, devising a protocol to test your hypothesis, and analyzing the results. Within the experimentation process it will be important to identify the independent variable, the dependent variable, and standardized variables for each experiment.
Observations.
From the introduction and your reading, you have some background knowledge on enzyme structure and function. You also just observed the effects of catalase on the reaction in which hydrogen peroxide breaks down into water and oxygen.
From the objectives of this lab, our questions are as follows:
Based on the questions above, come up with some possible hypotheses. These should be general, not specific, statements that are possible answers to your questions.
Based on your hypotheses, design a set of experiments to test your hypotheses. Use your original experiment to shape your ideas. You have the following materials available:
Write your procedure to test each hypothesis. You should have three procedures, one for each hypothesis. Make sure your instructor checks your procedures before you continue.
Record your results—you may want to draw tables. Also record any observations you make. Interpret your results to draw conclusions.
Scientists generally communicate their research findings in written reports. Save the things that you have done above. You will be use them to write a lab report a little later in the course.
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The .gov means it’s official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
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Olga giraldo.
1 Ontology Engineering Group, Campus de Montegancedo, Boadilla del Monte, Universidad Politécnica de Madrid, Madrid, Spain
2 Technische Universität Graz, Graz, Austria
Associated data.
The following information was supplied regarding data availability:
Federico López Gómez, Alexander Garcia & Olga Giraldo. (2018, March 26). SMARTProtocols/SMARTProtocols.github.io: First release of SMARTProtocols.github.io (Version v1.0.0). Zenodo. http://doi.org/10.5281/zenodo.1207846 .
Olga Giraldo. (2018, March 22). oxgiraldo/SMART-Protocols: First release of SMART-Protocols repository (Version v1.0.0). Zenodo. http://doi.org/10.5281/zenodo.1205247 .
Olga Giraldo, Alexander Garcia, & Oscar Corcho. (2018). Survey - reporting an experimental protocol [Data set]. Zenodo. http://doi.org/10.5281/zenodo.1204916 .
Olga Giraldo, Alexander Garcia, & Oscar Corcho. (2018). Guidelines for reporting experimental protocols [Data set]. Zenodo. http://doi.org/10.5281/zenodo.1204887 .
Olga Giraldo, Alexander Garcia, & Oscar Corcho. (2018). Corpus of protocols [Data set]. Zenodo. http://doi.org/10.5281/zenodo.1204838 .
Experimental protocols are key when planning, performing and publishing research in many disciplines, especially in relation to the reporting of materials and methods. However, they vary in their content, structure and associated data elements. This article presents a guideline for describing key content for reporting experimental protocols in the domain of life sciences, together with the methodology followed in order to develop such guideline. As part of our work, we propose a checklist that contains 17 data elements that we consider fundamental to facilitate the execution of the protocol. These data elements are formally described in the SMART Protocols ontology. By providing guidance for the key content to be reported, we aim (1) to make it easier for authors to report experimental protocols with necessary and sufficient information that allow others to reproduce an experiment, (2) to promote consistency across laboratories by delivering an adaptable set of data elements, and (3) to make it easier for reviewers and editors to measure the quality of submitted manuscripts against an established criteria. Our checklist focuses on the content, what should be included. Rather than advocating a specific format for protocols in life sciences, the checklist includes a full description of the key data elements that facilitate the execution of the protocol.
Experimental protocols are fundamental information structures that support the description of the processes by means of which results are generated in experimental research ( Giraldo et al., 2017 ; Freedman, Venugopalan & Wisman, 2017 ). Experimental protocols, often as part of “Materials and Methods” in scientific publications, are central for reproducibility; they should include all the necessary information for obtaining consistent results ( Casadevall & Fang, 2010 ; Festing & Altman, 2002 ). Although protocols are an important component when reporting experimental activities, their descriptions are often incomplete and vary across publishers and laboratories. For instance, when reporting reagents and equipment, researchers sometimes include catalog numbers and experimental parameters; they may also refer to these items in a generic manner, e.g., “ Dextran sulfate, Sigma-Aldrich ” ( Karlgren et al., 2009 ). Having this information is important because reagents usually vary in terms of purity, yield, pH, hydration state, grade, and possibly additional biochemical or biophysical features. Similarly, experimental protocols often include ambiguities such as “ Store the samples at room temperature until sample digestion ” ( Brandenburg et al., 2002 ); but, how many Celsius degrees? What is the estimated time for digesting the sample? Having this information available not only saves time and effort, it also makes it easier for researchers to reproduce experimental results; adequate and comprehensive reporting facilitates reproducibility ( Freedman, Venugopalan & Wisman, 2017 ; Baker, 2016 ).
Several efforts focus on building data storage infrastructures, e.g., 3TU. Datacentrum ( 4TU, 2017 ), CSIRO Data Access Portal ( CSIRO, 2017 ), Dryad ( Dryad, 2017 ), figshare ( Figshare, 2017 ), Dataverse ( King, 2007 ) and Zenodo ( Zenodo, 2017 ). These data repositories make it possible to review the data and evaluate whether the analysis and conclusions drawn are accurate. However, they do little to validate the quality and accuracy of the data itself. Evaluating research implies being able to obtain similar, if not identical results. Journals and funders are now asking for datasets to be publicly available for reuse and validation. Fully meeting this goal requires datasets to be endowed with auxiliary data providing contextual information e.g., methods used to derive such data ( Assante et al., 2016 ; Simmhan, Plale & Gannon, 2005 ). If data must be public and available, shouldn’t methods be equally public and available?
Illustrating the problem of adequate reporting, Moher et al. (2015) have pointed out that fewer than 20% of highly-cited publications have adequate descriptions of study design and analytic methods. In a similar vein, Vasilevsky et al. (2013) showed that 54% of biomedical research resources such as model organisms, antibodies, knockdown reagents (morpholinos or RNAi), constructs, and cell lines are not uniquely identifiable in the biomedical literature, regardless of journal Impact Factor. Accurate and comprehensive documentation for experimental activities is critical for patenting, as well as in cases of scientific misconduct. Having data available is important; knowing how the data were produced is just as important. Part of the problem lies in the heterogeneity of reporting structures; these may vary across laboratories in the same domain. Despite this variability, we want to know which data elements are common and uncommon across protocols; we use these elements as the basis for suggesting our guideline for reporting protocols. We have analyzed over 500 published and non-published experimental protocols, as well as guidelines for authors from journals publishing protocols. From this analysis we have derived a practical adaptable checklist for reporting experimental protocols.
Efforts such as the Structured, Transparent, Accessible Reporting (STAR) initiative ( Marcus, 2016 ; Cell Press, 2017 ) address the problem of structure and standardization when reporting methods. In a similar manner, The Minimum Information about a Cellular Assay (MIACA) ( MIACA, 2017 ), The Minimum Information about a Flow Cytometry Experiment (MIFlowCyt) ( Lee et al., 2008 ) and many other “minimal information” efforts deliver minimal data elements describing specific types of experiments. Soldatova et al. (2008) and Soldatova et al. (2014) proposes the EXACT ontology for representing experimental actions in experimental protocols; similarly, Giraldo et al. (2017) proposes the S e MA ntic R epresen T ation of Protocols ontology (henceforth SMART Protocols Ontology) an ontology for reporting experimental protocols and the corresponding workflows. These approaches are not minimal; they aim to be comprehensive in the description of the workflow, parameters, sample, instruments, reagents, hints, troubleshooting, and all the data elements that help to reproduce an experiment and describe experimental actions.
There are also complementary efforts addressing the problem of identifiers for reagents and equipment; for instance, the Resource Identification Initiative (RII) ( Force11, 2017 ), aims to help researchers sufficiently cite the key resources used to produce the scientific findings. In a similar vein, the Global Unique Device Identification Database (GUDID) ( NIH, 2018 ) has key device identification information for medical devices that have Unique Device Identifiers (UDI); the Antibody Registry ( Antibody Registry, 2018 ), gives researchers a way to universally identify antibodies used in their research, and also the Addgene web-application ( Addgene, 2018 ) makes it easy for researchers to identify plasmids. Having identifiers make it possible for researchers to be more accurate in their reporting by unequivocally pointing to the resource used or produced. The Resource Identification Portal ( RIP, 2018 ), makes it easier to navigate through available identifiers, researchers can search across all the sources from a single location.
In this paper, we present a guideline for reporting experimental protocols; we complement our guideline with a machine-processable checklist that helps researchers, reviewers and editors to measure the completeness of a protocol. Each data element in our guideline is represented in the SMART Protocols Ontology. This paper is organized as follows: we start by describing the materials and methods used to derive the resulting guidelines. In the “Results” section, we present examples indicating how to report each data element; a machine readable checklist in the JavaScript Object Notation (JSON) format is also presented in this section. We then discuss our work and present the conclusions.
We have analyzed: (i) guidelines for authors from journals publishing protocols ( Giraldo, Garcia & Corcho, 2018b ), (ii) our corpus of protocols ( Giraldo, Garcia & Corcho, 2018a ), (iii) a set of reporting structures proposed by minimal information projects available in the FairSharing catalog ( McQuilton et al., 2016 ), and (iv) relevant biomedical ontologies available in BioPortal ( Whetzel et al., 2011 ) and Ontobee ( Xiang et al., 2011 ). Our analysis was carried out by a domain expert, Olga Giraldo; she is an expert in text mining and biomedical ontologies with over ten years of experience in laboratory techniques. All the documents were read, and then data elements, subject areas, materials (e.g., sample, kits, solutions, reagents, etc.), and workflow information were identified. Resulting from this activity we established a baseline terminology, common and non common data elements, as well as patterns in the description of the workflows (e.g., information describing the steps and the order for the execution of the workflow).
Publishers usually have instructions for prospective authors; these indications tell authors what to include, the information that should be provided, and how it should be reported in the manuscript. In Table 1 we present the list of guidelines that were analyzed.
Journal | Guidelines for authors |
---|---|
BioTechniques (BioTech) | |
CSH protocols (CSH) | |
Current Protocols (CP) | |
Journal of Visualized Experiments (JoVE) | |
Nature Protocols (NP) | |
Springer Protocols (SP) | |
MethodsX | |
Bio-protocols (BP) | |
Journal of Biological Methods (JBM) |
Our corpus includes 530 published and unpublished protocols. Unpublished protocols (75 in total) were collected from four laboratories located at the International Center for Tropical Agriculture (CIAT) ( CIAT, 2017 ). The published protocols (455 in total) were gathered from the repository “Nature Protocol Exchange” ( NPE, 2017 ) and from 11 journals, namely: BioTechniques, Cold Spring Harbor Protocols, Current Protocols, Genetics and Molecular Research ( GMR, 2017 ), JoVE, Plant Methods ( BioMed Central, 2017 ), Plos One ( PLOS ONE, 2017 ), Springer Protocols, MethodsX, Bio-Protocol and the Journal of Biological Methods. The analyzed protocols comprise areas such as cell biology, molecular biology, immunology, and virology. The number of protocols from each journal is presented in Table 2 .
Source | Number of protocols |
---|---|
BioTechniques (BioTech) | 16 |
CSH protocols (CSH) | 267 |
Current Protocols (CP) | 31 |
Genetics and Molecular Research (GMR) | 5 |
Journal of Visualized Experiments (JoVE) | 21 |
Nature Protocols Exchange (NPE) | 39 |
Plant Methods (PM) | 12 |
Plos One (PO) | 5 |
Springer Protocols (SP) | 5 |
MethodsX | 7 |
Bio-protocols (BP) | 40 |
Journal of Biological Methods (JBM) | 7 |
Non-published protocols from CIAT | 75 |
We analyzed minimum information standards from the FairSharing catalog, e.g., MIAPPE ( MIAPPE, 2017 ), MIARE ( MIARE, 2017 ) and MIQE ( Bustin et al., 2009 ). See Table 3 for the complete list of minimum information models that we analyzed.
Standards | Description |
---|---|
Minimum Information about Plant Phenotyping Experiment (MIAPPE) | A reporting guideline for plant phenotyping experiments. |
CIMR: Plant Biology Context ( ) | A standard for reporting metabolomics experiments. |
The Gel Electrophoresis Markup Language (GelML) | A standard for representing gel electrophoresis experiments performed in proteomics investigations. |
Minimum Information about a Cellular Assay (MIACA) | A standardized description of cell-based functional assay projects. |
Minimum Information About an RNAi Experiment (MIARE) | A checklist describing the information that should be reported for an RNA interference experiment. |
The Minimum Information about a Flow Cytometry Experiment (MIFlowCyt) | This guideline describes the minimum information required to report flow cytometry (FCM) experiments. |
Minimum Information for Publication of Quantitative Real-Time PCR Experiments (MIQE) | This guideline describes the minimum information necessary for evaluating qPCR experiments. |
ARRIVE (Animal Research: Reporting of Experiments) ( ) | Initiative to improve the standard of reporting of research using animals. |
We paid special attention to the recommendations indicating how to describe specimens, reagents, instruments, software and other entities participating in different types of experiments. Ontologies available at Bioportal and Ontobee were also considered; we focused on ontologies modeling domains, e.g., bioassays (BAO), protocols (EXACT), experiments and investigations (OBI). We also focused on those modeling specific entities, e.g., organisms (NCBI Taxon), anatomical parts (UBERON), reagents or chemical compounds (ERO, ChEBI), instruments (OBI, BAO, EFO). The list of analyzed ontologies is presented in Table 4 .
Ontology | Description |
---|---|
The Ontology for Biomedical Investigations (OBI) ( ) | An ontology for the description of life-science and clinical investigations. |
The Information Artifact Ontology (IAO) ( ) | An ontology of information entities. |
The ontology of experiments (EXPO) ( ) | An ontology about scientific experiments. |
The ontology of experimental actions (EXACT) | An ontology representing experimental actions. |
The BioAssay Ontology (BAO) ( ) | An ontology describing biological assays. |
The Experimental Factor Ontology (EFO) ( ) | The ontology includes aspects of disease, anatomy, cell type, cell lines, chemical compounds and assay information. |
eagle-i resource ontology (ERO) | An ontology of research resources such as instruments, protocols, reagents, animal models and biospecimens. |
NCBI taxonomy (NCBITaxon) ( ) | An ontology representation of the NCBI organismal taxonomy. |
Chemical Entities of Biological Interest (ChEBI) ( ) | Classification of molecular entities of biological interest focusing on ‘small’ chemical compounds. |
Uberon multi-species anatomy ontology (UBERON) ( ) | A cross-species anatomy ontology covering animals and bridging multiple species-specific ontologies. |
Cell Line Ontology (CLO) ( ; ) | The ontology was developed to standardize and integrate cell line information. |
Developing the guideline entailed a series of activities; these were organized in the following stages: (i) analysis of guidelines for authors, (ii) analysis of protocols, (iii) analysis of Minimum Information (MI) standards and ontologies, and (iv) evaluation of the data elements from our guideline. For a detailed representation of our workflow, see Fig. 1
We manually reviewed instructions for authors from nine journals as presented in Table 1 . In this stage (step A in Fig. 1 ), we identified bibliographic data elements classified as “desirable information” in the analyzed guidelines. See Table 5 .
Bibliographic data elements | BioTech | NP | CP | JoVE | CSH | SP | BP | MethodsX | JBM |
---|---|---|---|---|---|---|---|---|---|
title/name | Y | Y | Y | Y | Y | Y | Y | Y | Y |
author name | Y | Y | Y | Y | Y | Y | Y | Y | Y |
author identifier (e.g., orcid) | N | N | N | N | N | N | N | N | N |
protocol identifier (DOI) | Y | Y | Y | Y | Y | Y | Y | Y | Y |
protocol source (retrieved from, modified from) | N | Y | N | N | N | N | N | N | N |
updates (corrections, retractions or other revisions) | N | N | N | N | N | N | N | N | N |
references/related publications | Y | Y | Y | Y | Y | Y | Y | Y | Y |
categories or keywords | Y | Y | Y | Y | Y | Y | Y | Y | Y |
In addition, we identified the rhetorical elements. These have been categorized in the guidelines for authors as: (i) required information (R), must be submitted with the manuscript; (ii) desirable information (D), should be submitted if available; and (iii) optional (O) or extra information. See Table 6 for more details.
Rhetorical/discourse elements | Bio-Tech | NP | CP | JoVE | CSH | SP | BP | MethodsX | JBM |
---|---|---|---|---|---|---|---|---|---|
Description of the protocol (objective, range of applications where the protocol can be used, advantages, limitations) | D | D | D | D | D | D | D | D | D |
Description of the sample tested (name; ID; strain, line or ecotype; developmental stage; organism part; growth conditions; treatment type; size) | NC | NC | D | NC | NC | NC | NC | NC | NC |
Reagents (name, vendor, catalog number) | R | D | D | D | R | D | R | NC | D |
Equipment (name, vendor, catalog number) | R | D | D | D | R | D | R | NC | D |
Recipes for solutions (name, final concentration, volume) | R | D | D | D | D | D | R | NC | D |
Procedure description | R | R | R | D | R | R | R | R | D |
Alternatives to performing specific steps | NC | NC | D | D | NC | D | NC | NC | NC |
Critical steps | R | NC | D | NC | NC | NC | NC | NC | NC |
Pause point | R | NC | NC | O | D | NC | NC | NC | NC |
Troubleshooting | R | O | R | O | D | D | NC | NC | D |
Caution/warnings | NC | NC | R | O | NC | D | NC | NC | D |
Execution time | NC | O | D | NC | NC | D | NC | NC | NC |
Storage conditions (reagents, recipes, samples) | R | NC | R | D | D | D | NC | NC | NC |
Results (figure, tables) | R | NC | R | R | D | R | D | NC | D |
In 2014, we started by manually reviewing 175 published and unpublished protocols; these were from domains such as cell biology, biotechnology, virology, biochemistry and pathology. From this collection, 75 are unpublished protocols and thus not available in the dataset for this paper. These unpublished protocols were collected from four laboratories located at the CIAT. In 2015, our corpus grew to 530; we included 355 published protocols gathered from one repository and eleven journals as listed in Table 2 . Our corpus of published protocols is: (i) identifiable, i.e., each document has a Digital Object Identifier (DOI) and (ii) in disciplines and areas related to the expertise provided by our domain experts, e.g., virology, pathology, biochemistry, biotechnology, plant biotechnology, cell biology, molecular and developmental biology and microbiology. In this stage, step B in Fig. 1 , we analyzed the content of the protocols; theory vs. practice was our main concern. We manually verified if published protocols were following the guidelines; if not, what was missing , what additional information was included? We also reviewed common data elements in unpublished protocols.
Biomedical sciences have an extensive body of work related to minimum information standards and reporting structures, e.g., those from the FairSharing initiative. We were interested in determining whether there was any relation to these resources. Our checklist includes the data elements that are common across these resources. We manually analyzed standards such as MIQE, used to describe qPCR assays; we also looked into MIACA, it provides guidelines to report cellular assays; ARRIVE, which provides detailed descriptions of experiments on animal models and MIAPPE, addressing the descriptions of experiments for plant phenotyping. See Table 3 for a complete list of the standards that we analyzed. Metadata, data, and reporting structures in biomedical documents are frequently related to ontological concepts. We also looked into relations between data elements and biomedical ontologies available in BioPortal and Ontobee. We focused on ontologies representing materials that are often found in protocols; for instance, organisms, anatomical parts (e.g., CLO, UBERON, NCBI Taxon), reagents or chemical compounds (e.g., ChEBI, ERO), and equipment (e.g., OBI, BAO, EFO). The complete list of the ontologies that we analyzed is presented in Table 4 .
The first draft is the main output from the initial analysis of instructions for authors, experimental protocols, MI standards and ontologies, see (step D in Fig. 1 ). The data elements were organized into four categories: bibliographic data elements such as title, authors; descriptive data elements such as purpose, application; data elements for materials, e.g., sample, reagents, equipment; and data elements for procedures, e.g., critical steps, Troubleshooting. The role of the authors, provenance and properties describing the sample (e.g., organism part, amount of the sample, etc.) were considered in this first draft. In addition properties like “name”, “manufacturer or vendor” and “identifier” were proposed to describe equipment, reagents and kits.
This stage entailed three activities. The first activity was carried out at CIAT with the participation of 19 domain experts in areas such as virology, pathology, biochemistry, and plant biotechnology. The input of this activity was the checklist V. 0.1 (see step E in Fig. 1 ). This evaluation focused on “ What information is necessary and sufficient for reporting an experimental protocol? ”; the discussion also addressed data elements that were not initially part of guidelines for authors -e.g., consumables. The result of this activity was the version 0.2 of the checklist; domain experts suggested to use an online survey for further validation. This survey was designed to enrich and validate the checklist V. 0.2. We used a Google survey that was circulated over mailing lists; participants did not have to disclose their identity (see step F in Fig. 1 ). A final meeting was organized with those who participated in workshops, as well as in the survey (23 in total) to discuss the results of the online poll. The discussion focused on the question: Should the checklist include data elements not considered by the majority of participants? Participants were presented with use cases where infrequent data elements are relevant in their working areas. It was decided to include all infrequent data elements; domain experts concluded that this guideline was a comprehensive checklist a opposed to a minimal information. Also, after discussing infrequent data elements it was concluded that the importance of a data element should not bear a direct relation to its popularity. The analogy used was that of an editorial council; some data elements needed to be included regardless of the popularity as an editorial decision. The output of this activity was the checklist V. 1.0. The survey and its responses are available at ( Giraldo, Garcia & Corcho, 2018c ). This current version includes a new bibliographic element “license of the protocol”, as well as the property “equipment configuration” associated to the datum equipment. The properties: alternative, optional and parallel steps were added to describe the procedure. In addition, the datum “PCR primers” was removed from the checklist, it is specific and therefore should be the product of a community specialization as opposed to part of a generic guideline.
Our results are summarized in Table 7 ; it includes all the data elements resulting from the process illustrated in Fig. 1 . We have also implemented our checklist as an online tool that generates data in the JSON format and presents an indicator of completeness based on the checked data elements; the tool is available at https://smartprotocols.github.io/checklist1.0 ( Gómez, alexander & Giraldo, 2018 ). Below, we present a complete description of the data elements in our checklist. We have organized the data elements in four categories, namely: (i) bibliographic data elements, (ii) discourse data elements, (iii) data elements for materials, and iv) data elements for the procedure. Ours is a comprehensive checklist, the data elements must be reported whenever applicable.
Data element | Property |
---|---|
Title of the protocol | |
Author | Name |
Identifier | |
Version number | |
License of the protocol | |
Provenance of the protocol | |
Overall objective or purpose | |
Application of the protocol | |
Advantage(s) of the protocol | |
Limitation(s) of the protocol | |
Organism | Whole organism / Organism part |
Sample/organism identifier | |
Strain, genotype or line | |
Amount of Bio-Source | |
Developmental stage | |
Bio-source supplier | |
Growth substrates | |
Growth environment | |
Growth time | |
Sample pre-treatment or sample preparation | |
Laboratory equipment | Name |
Manufacturer or vendor (including homepage) | |
Identifier (catalog number or model) | |
Equipment configuration | |
Laboratory consumable | Name |
Manufacturer or vendor (including homepage) | |
Identifier (catalog number) | |
Reagent | Name |
Manufacturer or vendor (including homepage) | |
Identifier (catalog number) | |
Kit | Name |
Manufacturer or vendor (including homepage) | |
Identifier (catalog number) | |
Recipe for solution | Name |
Reagent or chemical compound name | |
Initial concentration of a chemical compound | |
Final concentration of chemical compound | |
Storage conditions | |
Cautions | |
Hints | |
Software | Name |
Version number | |
Homepage | |
Procedure | List of steps in numerical order |
Alternative/Optional/Parallel steps | |
Critical steps | |
Pause point | |
Timing | |
Hints | |
Troubleshooting |
From the guidelines for authors, the datum “author identifier” was not considered, nor was this data element found in the analyzed protocols. The “provenance” is proposed as “desirable information” in only two of the guidelines (Nature Protocols and Bio-protocols), as well as “updates of the protocol” (Cold Spring Harbor Protocols and Bio-protocols). A total of 72.5% (29) of the protocols available in our Bio-protocols collection and 61.5% (24) of the protocols available in our Nature Protocols Exchange collection reported the provenance ( Fig. 2 ). None of the protocols collected from Cold Spring Harbor Protocols or Bio-protocols had been updated–last checked December 2017.
NC, Not Considered in guidelines; D, Desirable information if this is available.
As a result of the workshops, domain experts exposed the importance of including these three data elements in our checklist. For instance, readers sometimes need to contact the authors to ask about specific information (quantity of the sample used, the storage conditions of a solution prepared in the lab, etc.); occasionally, the correspondent author does not respond because he/she has changed his/her email address, and searching for the full name could retrieve multiple results. By using author IDs, this situation could be resolved. The experts asserted that well-documented provenance helps them to know where the protocol comes from and whether it has changed. For example, domain experts expressed their interest in knowing where a particular protocol was published for the first time, who has reused it, how many research papers have used it, how many people have modified it, etc. In a similar way, domain experts also expressed the need for a version control system that could help them to know and understand how, where and why the protocol has changed. For example, researchers are interested in tracking changes in quantities, reagents, instruments, hints, etc. For a complete description of the bibliographic data elements proposed in our checklist, see below.
Title. The title should be informative, explicit, and concise (50 words or fewer). The use of ambiguous terminology and trivial adjectives or adverbs (e.g., novel, rapid, efficient, inexpensive, or their synonyms) should be avoided. The use of numerical values, abbreviations, acronyms, and trademarked or copyrighted product names is discouraged. This definition was adapted from BioTechniques ( Giraldo, Garcia & Corcho, 2018b ). In Table 8 , we present examples illustrating how to define the title.
ambiguous title | A protocol for extraction of from bacteria and yeast. | Protocol available at |
comprehensible title | Extraction of nucleic acids from yeast cells and plant tissues using ethanol as medium for sample preservation and cell disruption. | Protocol available at |
Issues in the ambiguous tittle:
Author name and author identifier. The full name(s) of the author(s) is required together with an author ID, e.g., ORCID ( ORCID, 2017 ) or research ID ( ResearcherID, 2017 ). The role of each author is also required; depending on the domain, there may be several roles. It is important to use a simple word that describes who did what. Publishers, laboratories, and authors should enforce the use of an “author contribution section” to identify the role of each author. We have identified two roles that are common across our corpus of documents.
Updating the protocol. The peer-reviewed and non peer-reviewed repositories of protocols should encourage authors to submit updated versions of their protocols; these may be corrections, retractions, or other revisions. Extensive modifications to existing protocols could be published as adapted versions and should be linked to the original protocol. We recommended to promote the use of a version control system; in this paper we suggest to use the version control guidelines proposed by the National Institute of Health (NIH) ( NIH, 2017 ).
Provenance of the protocol. The provenance is used to indicate whether or not the protocol results from modifying a previous one. The provenance also indicates whether the protocol comes from a repository, e.g., Nature Protocols Exchange, protocols.io ( Teytelman et al., 2016 ), or a journal like JoVE, MethodsX, or Bio-Protocols. The former refers to adaptations of the protocol. The latter indicates where the protocol comes from. See Table 9 .
example | Protocol available at |
License of the protocol. The protocols should include a license. Whether as part of a publication or, just as an internal document, researchers share, adapt and reuse protocols. The terms of the license should facilitate and make clear the legal framework for these activities.
Here, we present the elements considered necessary to understand the suitability of a protocol. They are the “overall objective or purpose”, “applications”, “advantages,” and “limitations”. 100% of the analyzed guidelines for author suggest the inclusion of these four elements in the abstract or introduction section. However, one or more of these four elements were not reported. For example, “limitations” was reported in only 20% of the protocols from Genetic and Molecular Research and PLOS One, and in 40% of the protocols from Springer. See Fig. 3 .
Interestingly, 83% of the respondents considered the “limitations” to be a data element that is necessary when reporting a protocol. In the last meeting, participants considered that “limitations” represents an opportunity to make suggestions for further improvements. Another data element discussed was “advantages”; 43% of the respondents considered the “advantages” as a data element that is necessary to be reported in a protocol. In the last meeting, all participants agreed that “advantages” (where applicable) could help us to compare a protocol with other alternatives commonly used to achieve the same result. For a complete description of the discourse data elements proposed in our checklist, see below.
Overall objective or Purpose. The description of the objective should make it possible for readers to decide on the suitability of the protocol for their experimental problem. See Table 10 .
Discourse data element | Example | Source |
---|---|---|
Overall objective/ Purpose | Reagent or columns.” | Protocol available at |
Application | Protocol available at | |
Advantage(s) | Protocol available at | |
Limitation(s) | Protocol available at |
Application of the protocol. This information should indicate the range of techniques where the protocol could be applied. See Table 10 .
Advantage(s) of the protocol. Here, the advantages of a protocol compared to other alternatives should be discussed. See Table 10 . Where applicable, references should be made to alternative methods that are commonly used to achieve the same result.
Limitation(s) of the protocol. This datum includes a discussion of the limitations of the protocol. This should also indicate the situations in which the protocol could be unreliable or unsuccessful. See Table 10 .
From the analyzed guidelines for authors, the datum “sample description” was considered only in the Current Protocols guidelines. The “laboratory consumables or supplies” datum was not included in any of the analyzed guidelines. See Fig. 4 .
NC, Not Considered in guidelines; D, Desirable information if this is available; R, Required information.
Our Current Protocols collection includes documents about toxicology, microbiology, magnetic resonance imaging, cytometry, chemistry, cell biology, human genetics, neuroscience, immunology, pharmacology, protein, and biochemistry; for these protocols the input is a biological or biochemical sample. This collection also includes protocols in bioinformatics with data as the input. 100% of the protocols from our Current Protocols collection includes information about the input of the protocol (biological/biochemical sample or data). In addition, 87% of protocols from this collection include a list of materials or resources (reagents, equipment, consumables, software, etc.).
We also analyzed the protocols from our MethodsX collection. We found that despite the exclusion of the sample description in guidelines for authors, the authors included this information in their protocols. Unfortunately, these protocols do not include a list of materials. Only 29% of the protocols reported a partial list of materials. For example, the protocol published by Vingataramin & Frost (2015) , includes a list of recommended equipment but does not list any of the reagents, consumables, or other resources mentioned in the protocol instructions. See Fig. 5 .
Domain experts considered that the input of the protocol (biological/biochemical sample or data) needs an accurate description; the granularity of the description varies depending on the domain. If such description is not available then the reproducibility could be affected. In addition, domain experts strongly suggested to include consumables in the checklist. It was a general surprise not to find these data elements in the guidelines for authors that we analyzed. Domain experts shared with us bad experiences caused by the lack of information about the type of consumables. Some of the incidents that may arise from the lack of this information include: (i) cross contamination, when no information suggesting the use of filtered pipet tips is available; (ii) misuse of containers, when no information about the use of containers resistant to extreme temperatures and/or impacts is available; (iii) misuse of containers, when a container made of a specific material should be used, e.g., glass vs. plastic vs. metal. This is critical information; researchers need to know if reagents or solutions prepared in the laboratory require some specific type of containers in order to avoid unnecessary reactions altering the result of the assay. Presented below is the set of data elements related to materials or resources used for carrying out the execution of a protocol.
Sample. This is the role played by a biological substance; the sample is an experimental input to a protocol. The information required depends on the type of sample being described and the requirements from different communities. Here, we present the data elements for samples commonly used across the protocols and guidelines that we analyzed.
Laboratory equipment. The laboratory equipment includes apparatus and instruments that are used in diagnostic, surgical, therapeutic, and experimental procedures. In this subsection, all necessary equipment should be listed; manufacturer name or vendor (including the homepage), catalog number (or model), and configuration of the equipment should be part of this data element. See Table 11 .
Protocol available at |
Laboratory consumables or supplies. The laboratory consumables include, amongst others, disposable pipettes, beakers, funnels, test tubes for accurate and precise measurement, disposable gloves, and face masks for safety in the laboratory. In this subsection, a list with all the consumables necessary to carry out the protocol should be presented with manufacturer name (including the homepage) and catalog number. See Table 12 .
Filter paper | Protocol available at | |
Filter paper (GE, catalog number: 10311611) | Protocol available at |
Recipe for solutions. A recipe for solutions is a set of instructions for preparing a particular solution, media, buffer, etc. The recipe for solutions should include the list of all necessary ingredients (chemical compounds, substance, etc.), initial and final concentrations, pH, storage conditions, cautions, and hints. Ready-to-use reagents do not need to be listed in this category; all purchased reagents that require modification (e.g., a dilution or addition of β -mercaptoethanol) should be listed. See Table 13 for more information.
See in the section recipes, the recipe 1 (PBS) | Protocol available at | |
Phosphate-buffered saline (PBS) recipe | Protocol available at |
Reagents. A reagent is a substance used in a chemical reaction to detect, measure, examine, or produce other substances. List all the reagents used when performing the protocol, the vendor name (including homepage), and catalog number. Reagents that are purchased ready-to-use should be listed in this section. See Table 14 .
Dextran sulfate, Sigma-Aldrich | Protocol available at | |
Dextran sulfate sodium salt from , Sigma-Aldrich, D8906-5G | Protocol available at |
Kits. A kit is a gear consisting of a set of articles or tools for a specific purpose. List all the kits used when carrying out the protocol, the vendor name (including homepage), and catalog number.
Software. Software is composed of a series of instructions that can be interpreted or directly executed by a processing unit. In this subsection, please list software used in the experiment including the version, as well as where to obtain it.
All the analyzed guidelines include recommendations about how to document the instructions; for example, list the steps in numerical order, use active tense, organize the procedures in major stages, etc. However, information about documentation of alternative, optional, or parallel steps (where applicable) and alert messages such as critical steps, pause point, and execution time was infrequent (available in less than 40% of the guidelines). See Fig. 6 .
NC, Not Considered in guidelines; O, Optional information; D, Desirable information if this is available; R, Required information.
We chose a subset of protocols (12 from our Plant Methods collection, 7 from our Biotechniques collection, and five unpublished protocols from CIAT) to review which data elements about the procedure were documented. 100% of the protocols have steps organized in major stages. 100% of the unpublished protocols list the steps in numerical order, and nearly 60% of the protocols from Plant Methods and Biotechniques followed this recommendation. Alert messages were included in 67% of the Plant Methods protocols and in 14% of the Biotechniques protocols. Neither of the five unpublished protocols included alert messages. Troubleshooting was reported in just a few protocols; this datum was available in 8% of the Plant Methods protocols and in 14% of the Biotechniques protocols. See Fig. 7 .
In this stage, the discussion with domain experts started with the description of steps. In some protocols, the steps are poorly described; for instance, some of them include working temperatures, e.g., cold room, on ice, room temperature; but, what exactly do they mean? Steps involving centrifugation, incubation, washing, etc., should specify conditions, e.g., time, temperature, speed (rpm or g), number of washes, etc. For experts, alert messages and troubleshooting (where applicable) complement the description of steps and facilitate a correct execution. This opinion coincides with the results of the survey, where troubleshooting and alert messages such as critical steps, pause points, and timing were considered relevant by 83%–87% of the respondents. The set of data elements related to the procedure is presented below.
For centrifugation steps, specify time, temperature, and speed (rpm or g). Always state whether to discard/keep the supernatant/pellet. For incubations, specify time, temperature, and type of incubator. For washes, specify conditions e.g., temperature, washing solution and volume, specific number of washes, etc.
Useful auxiliary information should be included in the form of “alert messages”. The goal is to remind or alert the user of a protocol with respect to issues that may arise when executing a step. These messages may cover special tips or hints for performing a step successfully, alternate ways to perform the step, warnings regarding hazardous materials or other safety conditions, time considerations. For instance, pause points, speed at which the step must be performed and storage information (temperature, maximum duration) ( Wiley’s Current Protocols, 2012 ).
Alert message | Step | Note | Source |
---|---|---|---|
Critical step | Protocol available at | ||
Pause point | Protocol available at | ||
Timing | Protocol available at | ||
Hint | Protocol available at |
The data elements proposed in our guideline are represented in the SMART Protocols Ontology. This ontology was developed to facilitate the semantic representation of experimental protocols. Our ontology reuses the Basic Formal Ontology (BFO) ( IFOMIS, 2018 ) and the Relation Ontology (RO) ( Smith et al., 2005 ) to characterize concepts. In addition, each term in the SMART Protocols ontology is represented with annotation properties imported from the OBI Minimal metadata. The classes and properties are represented by their respective labels to facilitate the readability; the prefix indicates the provenance for each term. Our ontology is organized in two modules. The document module represents the metadata necessary and sufficient for reporting a protocol. The workflow module represents the executable elements of a protocol to be carried out and maintained by humans. Figure 8 presents the hierarchical organization of data elements into the SMART Protocols Ontology.
In this paper, we have described 17 data elements that can be used to improve the reporting structure of protocols. Our work is based on the analysis of 530 published and non-published protocols, guidelines for authors, and suggested reporting structures. We examined guidelines for authors from journals that specialize in publishing experimental protocols, e.g., Bio-protocols, Cold Spring Harbor Protocols, MethodsX, Nature Protocols, and Plant Methods (Methodology). Although JoVE ( JoVE, 2017 ) is a video methods journal, its guidelines for authors were also considered. Online repositories were also studied; these resources deliver an innovative approach for the publication of protocols by offering platforms tailored for this kind of document. For instance, protocols.io ( protocols.io, 2018 ) structures the protocol by using specific data elements and treats the protocol as a social object, thus facilitating sharing. It also makes it possible to have version control over the document. Protocol Exchange from Nature Protocols is an open repository where users upload, organize, comment, and share their protocols. Our guideline has also benefited from the input from a group of researchers whose primary interest is having reproducible protocols. By analyzing reporting structures and guidelines for authors, we are contributing to the homogenization of data elements that should be reported as part of experimental protocols. Improving the reporting structure of experimental protocols will add the necessary layer of information that should accompany the data that is currently being deposited into data repositories.
Ours was an iterative development process; drafts were reviewed and analyzed, and then improved versions were produced. This made it easier for us to make effective use of the time that domain experts had available. Working with experimental protocols that were known by our group of domain experts helped us to engage them in the iterations. Also, for the domain experts who worked with us during the workshops, there was a pre-existing interest in standardizing their reporting structures. Reporting guidelines are not an accepted norm in biology ( MIBBI, 2017 ); however, experimental protocols are part of the daily activities for most biologists. They are familiar with these documents, the benefits of standardization are easy for them to understand. From our experience at CIAT, once researchers were presented with a standardized format that they could extend and manage with minimal overhead, they adopted it. The early engagement with domain experts in the development process eased the initial adoption; they were familiar with the outcome and aware of the advantages of implementing this practice. However, maintaining the use of the guideline requires more than just availability of the guideline; the long-term use of these instruments requires an institutional policy in data stewardship. Our approach builds upon previous experiences; in our case, the guidelines presented in this paper are a tool that was conceived by researchers as part of their reporting workflow, thus adding a minimal burden on their workload. As domain experts were working with the guideline, they were also gaining familiarity with the Minimum Information for Biological and Biomedical Investigations (MIBBI) ( MIBBI, 2017 ) that were applicable to their experiments. This made it possible for us to also discuss the relation between MIBBIs and the content in the experimental protocols.
The quality of the information reported in experimental protocols and methods is a general cause for concern. Poorly described methods generate poorly reproducible research. In a study conducted by Flórez-Vargas et al. (2014) in Trypanosoma experiments, they report that none of the investigated articles met all the criteria that should be reported in these kinds of experiments. The study reported by Kilkenny et al. (2009) has similar results leading to similar conclusions; key metadata elements are not always reported by researchers. The widespread availability of key metadata elements in ontologies, guidelines, minimal information models, and reporting structures was discussed. These were, from the onset, understood as reusable sources of information. Domain experts understand that they were building on previous experiences; having examples of use is helpful in understanding how to adapt or reuse from existing resources. This helps them to understand the rationale of each data element within the context of their own practice. For us, being able to consult previous experiences was also an advantage. Sharing protocols is a common practice amongst researchers from within the same laboratories or collaborating in the same experiments or projects. However, there are limitations in sharing protocols, not necessarily related to the lack of reporting standards. They are, for instance, related to patenting and intellectual property issues, as well as to giving away competitive advantages implicit in the method.
During our development process, we considered the SMART Protocols ontology ( Giraldo et al., 2017 ); it reuses terminology from OBI, IAO, EXACT, ChEBI, NCBI taxonomy, and other ontologies. Our metadata elements have been mapped to the SMART Protocols ontology; the metadata elements in our guideline could also be mapped to resources on the web such as PubChem ( Kim et al., 2016 ) ( Wang et al., 2017 ) and the Taxonomy database from UniProt ( UniProt, 2017 ). Our implementation of the checklist illustrates how it could be used as an online tool to generate a complement to the metadata that is usually available with published protocols. The content of the protocol does not need to be displayed; key metadata elements are made available together with the standard bibliographic metadata. Laboratories could adapt the online tool to their specific reporting structures. Having a checklist made it easier for the domain experts to validate their protocols. Machine validation is preferable, but such mechanisms require documents to be machine-processable beyond that which our domain experts were able to generate. Domain experts were using the guideline to implement simple Microsoft Word reporting templates. Our checklist does not include aspects inherent to each possible type of experiment such as those available in the MIBBIs; these are based on the minimal common denominator for specific experiments. Both approaches complement each other; where MIBBIs offer specificity, our guideline provides a context that is general enough for facilitating reproducibility and adequate reporting without interfering with records such as those commonly managed by Laboratory Information Management Systems.
In laboratories, experimental protocols are released and periodically undergo revisions until they are released again. These documents follow the publication model put forward by Carole Goble, “ Don’t publish, release ” with strict versioning, changes, and forks ( Goble, 2017 ). Experimental protocols are essentially executable workflows for which identifiers for equipment, reagents, and samples need to be resolved against the Web. The use of unique identifiers can’t be underestimated when supporting adequate reporting; identifiers remove ambiguity for key resources and make it possible for software agents to resolve and enrich these entities. The workflows in protocols are mostly followed by humans, but in the future, robots may be executing experiments ( Yachie, Consortium & Natsume, 2017 ); it makes sense to investigate other publication paradigms for these documents. The workflow nature of these documents is more suitable for a fully machine-processable or -actionable document. The workflows should be intelligible for humans and processable by machines; thus, facilitating the transition to fully automated laboratory paradigms. Entities and executable elements should be declared and characterized from the onset. The document should be “born semantic” and thus inter-operable with the larger web of data. In this way post-publication and linguistic processing activities, such as Named Entity Recognition and annotation, could be more focused.
Currently, when protocols are published, they are treated like any other scientific publication. Little attention is paid to the workflow nature implicit in this kind of document, or to the chain of provenance indicating where it comes from and how it has changed. The protocol is understood as a text-based narrative instead of a self-descriptive Findable Accessible Interoperable and Reusable (FAIR) ( Wilkinson et al., 2016 ) compliant document. There are differences across the examined publications, e.g., JoVE builds the narrative around video, whereas Bio-protocols, MethodsX, Nature Protocols, and Plant Methods primarily rely on a text-based narrative. The protocol is, however, a particular type of publication; it is slightly different from other scientific articles. An experimental protocol is a document that is kept “alive” after it has been published. The protocols are routinely used in laboratory activities, and researchers often improve and adapt them, for instance, by extending the type of samples that can be tested, reducing timing, minimizing the quantity of certain reagents without altering the results, adding new recipes, etc. The issues found in reporting methods probably stem, at least in part, from the current structure of scientific publishing, which is not adequate to effectively communicate complex experimental methods ( Flórez-Vargas et al., 2014 ).
Experimental research should be reproducible whenever possible. Having precise descriptions of the protocols is a step in that direction. Our work addresses the problem of adequate reporting for experimental protocols. It builds upon previous work, as well as over an exhaustive analysis of published and unpublished protocols and guidelines for authors. There is value in guidelines because they indicate how to report; having examples of use facilitate how to adapt them. The guideline we present in this paper can be adapted to address the needs of specific communities. Improving reporting structures requires collective efforts from authors, peer reviewers, editors, and funding bodies. There is no “one size that fits all.” The improvement will be incremental; as guidelines and minimal information models are presented, they will be evaluated, adapted, and re-deployed.
Authors should be aware of the importance of experimental protocols in the research life-cycle. Experimental protocols ought to be reused and modified, and derivative works are to be expected. This should be considered by authors before publishing their protocols; the terms of use and licenses are the choice of the publisher, but where to publish is the choice of the author. Terms of use and licenses forbidding “reuse”, “reproduce”, “modify”, or “make derivative works based upon” should be avoided. Such restrictions are an impediment to the ability of researchers to use the protocols in their most natural way, which is adapting and reusing them for different purposes –not to mention sharing, which is a common practice among researchers. Protocols represent concrete “know-how” in the biomedical domain. Similarly, publishers should adhere to the principle of encouraging authors to make protocols available, for instance, as preprints or in repositories for protocols or journals. Publishers should enforce the use of repository or journal publishing protocols. Publishers require or encourage data to be available; the same principle should be applied to protocols. Experimental protocols are essential when reproducing or replicating an experiment; data is not contextualized unless the protocols used to derive the data are available.
This work is related to the SMART Protocols project. Ultimately we want: (1) to enable authors to report experimental protocols with necessary and sufficient information that allows others to reproduce an experiment, (2) to ensure that every data item is resolvable against resources in the web of data, and (3) to make the protocols available in RDF, JSON, and HTML as web native objects. We are currently working on a publication platform based on linked data for experimental protocols. Our approach is simple, we consider that protocols should be born semantics and FAIR.
Special thanks to the research staff at CIAT; in particular, we want to express our gratitude to those who participated in the workshops, survey and discussions. We also want to thank Melissa Carrion for her useful comments and proof-reading. Finally, we would like to thank the editor and reviewers (Leonid Teytelman, Philippe Rocca-Serra and Tom Gillespie) for their valuable comments and suggestions to improve the manuscript.
This work was supported by the EU project Datos4.0 (No. C161046002). Olga Giraldo has been funded by the I+D+i pre doctoral grant from the UPM, and the Predoctoral grant from the I+D+i program from the Universidad Politécnica de Madrid. Alexander Garcia has been funded by the KOPAR project, H2020-MSCA-IF-2014, Grant Agreement No. 655009. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors declare there are no competing interests.
Olga Giraldo conceived and designed the experiments, performed the experiments, analyzed the data, contributed reagents/materials/analysis tools, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft.
Alexander Garcia contributed reagents/materials/analysis tools, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft, alexander supervised the research and was a constant springboard for discussion and ideas wrt the checklist and methods.
Oscar Corcho reviewed drafts of the paper, and approved the final draft.
Stay updated on the wildfire impacts to hunting areas in northeast Wyoming
CHEYENNE — On Sept. 3, the Wyoming Game and Fish Department, through the Wyoming State Veterinary Laboratory, confirmed a case of anthrax in a dead moose in Carbon County. The Wyoming Livestock Board recently informed Game and Fish that cattle near Elk Mountain have tested positive for anthrax.
Anthrax is a naturally occurring bacterial disease that can be transmitted between livestock, wildlife and humans. It is most commonly seen in herbivores, including cattle, deer and bison (elk, moose and pronghorn are also susceptible). Carnivores tend to be less at risk and may display higher resilience to the disease. The spores can persist in the ground for decades and emerge when the ground is disturbed or flooded. Disturbance is common in summer months when conditions may alternate between rain and hot, dry weather, allowing spores to be released from contaminated soil and ingested by livestock or wildlife.
This recent detection in a moose is the only documented case reported in wildlife at this time. The last confirmed case of anthrax in wildlife in Wyoming was in 1956 in Sublette County.
Game and Fish is advising hunters and the public to take the following precautions:
Game and Fish will continue to monitor the situation and assess impacts to wildlife. If changes occur that require further action, hunters will receive updates through emails and posts on the Game and Fish website.
For questions, please consult the following list of resources:
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Wyoming Livestock Board | Occurrences in cattle and area affected | 307-777-7515
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Wyoming Department of Health | Human health and safety concerns | 307-777-7656
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Wyoming Game and Fish Department | Wildlife and hunting concerns | Wildlife Health Lab: 307-745-5865 Regional Office: 307-745-4046 |
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Responsible for assisting with the setup of lab equipment, instructional materials, and lab resources which are utilized in the Department.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform the essential duties and responsibilities listed above. The qualifications listed below are representative of the education, experience, knowledge, skills, and/or abilities required.
High School Diploma or GED required.
1 year experience in an educational lab setting or related area preferred.
KNOWLEDGE, SKILLS AND ABILITIES
This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow any other job-related instructions and to perform any other job-related duties requested by their supervisor.
This job description may be revised upon development of other duties and changes in responsibilities.
The Organization
Houston Community College (HCC) is an open-admission, public institution of higher education offering a high-quality, affordable education for academic advancement, workforce training, career development and lifelong learning to prepare individuals in our diverse communities for life and work in a global and technological society. We’re proud to say that 98 percent of our graduates step into a job in their field of study immediately upon graduation. One of the largest community colleges in the nation, HCC has served the Greater Houston area for over four decades. Accredited by the Southern Association of Colleges and Schools, and the Schools Commission on Colleges, we offer 300+ associate degree and certificate programs to 75,000+ students across 13 Centers of Excellence and online each semester. We are proud to be No.1 among all community colleges in the nation in providing associate degrees to minorities and No.1 in educating international students, with 10.4 percent of our student population from outside the USA. Our vision is to become the Employer of Choice in support of our mission for Student Success by attracting, retaining and motivating the best employees.
The Team Some of the brightest minds in academics and business are choosing HCC as their home. When you join our talented team, you’ll play a special role as teacher, mentor and academic advisor. We’ll support you in your professional development as you contribute your knowledge and expertise to HCC, our students and the community.
Houston is a city with limitless possibilities:
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Agenda-setting intelligence, analysis and advice for the global fashion community.
Ginning, blowing, carding, drawing, roving, spinning, weaving, dyeing, cutting, sewing, ironing, shipping and trucking — all the steps it took to turn some cotton bolls into your T-shirt. Those processes also contribute the most to the planet-warming impact of the clothing fibre.
Growing cotton bolls itself sucks up huge amounts of water, pesticides and fertilisers. For all the water you’ll ever use to wash your cotton T-shirt over its entire lifetime, it will have taken 50 times as much water to grow the cotton that went into it. Cotton uses about 2.3 percent of global arable land and accounts for 16 percent for all insecticide sales. And the fashion industry has been forced to reckon with allegations of forced labor and poor working conditions in certain cotton-harvesting regions.
Boston-based startup Galy says its found an alternative that avoids all of these problems by growing cotton in a lab. The company shared an evaluation by environmental consultancy Quantis to show that, at an industrial scale, its process reduces water use by 99 percent, land use by 97 percent and the negative impact of fertilisers by 91 percent when compared with conventional cotton.
Brazil-born Luciano Bueno, chief executive officer of Galy, founded the company in 2019. But cotton has featured in his business life for much longer. “I started selling T-shirts door-to-door just to pay my bills in high school,” he said. His first job at Deloitte involved working for textile companies. His first company Horvath Co., which he founded in 2015, tried to develop sweat-resistant shirts.
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But after Horvath got stuck in an exclusivity deal, he took a break and studied entrepreneurship in Silicon Valley. It was during the heyday of fundraising for lab-grown meat startups that Bueno thought he should apply the same idea to cotton. It’s taken Galy a few years, but now the startup has shown enough progress to secure investments from huge cotton consumers: Hennes & Mauritz AB and Zara-owner Inditex SA.
Galy takes cells from a cotton plant, adds them to a large vat and feeds them sugar. After they have sufficiently multiplied, Galy technicians use their genetic understanding of the plant — which has been developed over decades of research — to activate certain genes and deactivate others. The result is the cell transforms and elongates into a cotton fibre.
So far, Galy has only been able to make a few kilograms of vat-grown cotton. If it can make more at scale, the company has big dreams to also make lab-grown cocoa and coffee powders. At its stall at the Breakthrough Energy Summit in London in June, Galy showed off all three products.
Buyers of cotton care about strand length, strength and purity. Galy already has purity given the process happens inside a vat and not in the open. That has helped it secure a $50-million deal with Suzuran Medical Inc. for medical-grade cotton, which Galy plans to supply over 10 years once it starts producing at industrial scale.
For clothing, Bueno says that Galy still needs to improve on strand length. That development will need investments in further research. In an announcement today, Galy said it had raised $33 million from Bill Gates-led Breakthrough Energy Ventures, H&M and Inditex — bringing the company’s total raise so far to $65 million.
Martin Ekenbark, lead of H&M’s circular innovation lab, said that the fast-fashion retailer is seeing a rise in the demand for cotton. “Customers prefer the hand feel of fabrics made with cotton,” he said.
After H&M stopped using cotton from China’s Xinjiang region in early 2021, following allegations of forced labor, it faced Chinese boycotts. H&M and other cotton consumers are keen to find solutions that can produce cotton without these risks.
Inditex has invested in more than 300 startups with the goal of finding new materials that have a lower impact on the environment, a company spokesperson said, and it’s now working with Galy to “enhance fiber quality through various proof-of-concept tests.”
Pound-for-pound cotton is much cheaper than meat and has a smaller market. The global cotton market is about $60 billion and cotton sells for a little more than $1 per kilogram, whereas the meat market is more than $1 trillion. That’s why Bueno’s focus is not just scaling up production, but also doing so at a tiny fraction of the cost of the process used for lab-grown meat.
There are a few things that help Galy. The plant cells only need sugar to multiply, rather than complex growth material used for meat. And given people aren’t going to be eating the cotton, Galy can use reactors that don’t have to adhere to as high hygiene standards.
The hurdles that remain aren’t small. Despite plenty of funding and investor enthusiasm, lab-grown companies have struggled to grow because of the finicky nature of biology and the struggle to sell the products at much higher cost than traditional alternatives. Galy will face the same problem and it’s raising money at a time when climate-tech investments have been shrinking. That’s one reason why Galy isn’t currently facing any major commercial competitors for developing lab-grown cotton.
Peter Turner, a partner at Breakthrough Energy Ventures, points out that Galy’s cotton today is at the same point lab-grown meat was in 2013. That’s when the Dutch researcher Mark Post made a 5-ounce burger that reportedly cost €250,000. That lead to a rapid growth in the number of startups chasing the prize, with funding for the sector peaking in 2021. Galy wouldn’t say what its cotton costs today.
“We fully expect competition to follow,” said Turner.
By Akshat Rathi
Learn more:
Better Cotton to Expand Due Diligence After Brazil Deforestation Investigation
Fashion’s biggest sustainable cotton certifier said it found no evidence of non-compliance at farms covered by its standard, but acknowledged weaknesses in its monitoring approach.
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The ultra-fast-fashion giant’s planet-warming emissions have nearly tripled in the last three years as its growth far outpaced other major fashion companies. In Shein's latest sustainability report, CEO Sky Xu says tackling emissions is “particularly critical."
The company said both cases had been “resolved swiftly,” with remediation steps including ending underage employees’ contracts, arranging medical checkups, and facilitating repatriation to parents or guardians as necessary.
Financial and political volatility are having a chilling effect on the industry’s environmental efforts. But failure to act now will bring bigger risks in the future, writes Kenneth P. Pucker.
Scientists say it’s increasingly likely 2024 will be the world’s hottest year on record, with rising temperatures carrying big implications from shopping malls to supply chains.
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Rocket lab usa.
The company's business is progressing as planned.
Rocket Lab USA ( RKLB 4.62% ) plans to go to Mars, and investors seem to think the stock could go along for the ride.
Shares of Rocket Lab climbed 19.7% in August, according to data provided by S&P Global Market Intelligence , on solid earnings and news about a high-profile mission.
Rocket Lab is part of a new generation of space companies reshaping the industry and taking share from incumbents. The company has quickly established itself as a leader , and is now trying to boldly go where few have gone before.
In August, the company reported strong year-over-year growth in the second quarter and a backlog of more than $1 billion in future business. Rocket Lab also announced it had built two spacecraft for the University of California Berkeley's Space Science Laboratory and NASA. The mission, which will travel to Mars, is part of a demonstration by Rocket Lab that it can do space missions at about one-tenth the cost of legacy space contractors. If successful, Rocket Lab should see significant demand for its services at these lower price points.
It is important to note that Rocket Lab is an early-stage, money-losing company with significant competition not just from large defense contractors but other start-ups as well. Rocket science is notoriously hard, and a lot can go wrong.
That said, Rocket Lab deserves plaudits for the progress management has made developing the business. Rocket Lab hopes to be a one-stop shop for government and corporate customers, able to design and manufacture satellites, launch them into space, and then maintain and control them from Earth.
A lot of the projected growth in the space industry assumes that companies who in the past had no space presence will eventually see value in having their own satellites in orbit. That requires a lower cost, and likely would favor Rocket Lab's approach compared to customers developing their own expertise in-house or dealing with a large number of vendors.
So, although this stock is not yet a sure thing, the company is well on its way toward proving out its concept. Demonstrating its value to NASA with this Mars mission is part of that process. The company continues to make progress in other areas as well, including the development of its new Neutron rocket that it hopes to launch in 2025 and which could eventually allow it to take larger payloads into space.
Given the risks involved in space, investors should remain cautious. But for those with a taste for high-risk, high-potential-reward type investments, Rocket Lab deserves consideration as part of a well-diversified portfolio .
Lou Whiteman has positions in Rocket Lab USA. The Motley Fool recommends Rocket Lab USA. The Motley Fool has a disclosure policy .
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As its name implies, PoE allows you to send both power and data to your devices over a single Ethernet cable. On paper, it may sound like a niche feature, as most servers, PCs, laptops, and NAS can’t be powered via an Ethernet cable. But if your computing environment consists of smart gadgets, Power over Ethernet can go from somewhat useful to an absolute game-changer – and here are four reasons why you should outfit your home lab with PoE technology.
Require an 8-port switch with PoE? This could be the one for you!
Why use two cables when you can go with just one.
The most obvious advantage of a PoE setup is that you’ll have fewer cables running around the house. Since most IoT and smart gadgets require both power and a data signal to operate, integrating PoE switches or injectors into your home lab can get rid of the barrel or USB connections required for power. As such, Power over Ethernet halves the number of connections in your home – and this can significantly reduce the cable clutter when you have multiple smart gadgets scattered all over the place.
No need to hunt for power outlets.
Even if your house has wall sockets around every corner, powering IP cameras and access points can be quite troublesome. Since they’re often fixed in hard-to-reach places, you’ll have to invest in long power adapters for these devices. And if you’re a fan of building cool projects with the Raspberry Pi and other SBCs , you won’t have to constantly seek out power outlets when testing your creations.
An easy way to reduce the legwork required to manage a home lab.
If you have multiple IoT devices powering your smart home, you’ll have to go through the tedious ritual of flipping the power switches when you wish to power them on. PoE switches can make this process a lot less painful, as you can turn your devices on or off over a remote connection. Plus, some of the more advanced PoE switches can even let you monitor the power consumption, voltage, and other aspects of the IoT devices connected to them.
Throw in a ups, and you won't have to worry about power outages anymore.
Besides adding to the mess of cables, one of the biggest drawbacks of using separate power connections is that you’ll be in a world of trouble if a particular outlet stops working. In case your house is as prone to power outages as mine, you’ll have to add a backup solution involving even more cables if you need constant access to your smart devices.
PoE provides an easy alternative to your blackout woes. All you have to do is plug an Uninterrupted Power Supply into your switch and voilà, you can continue using all devices compatible with PoE technology even during outages.
With all the pros of PoE technology, you might be worried about the extra cost of integrating Power over Ethernet provisions into your home lab . Sadly, PoE-compatible switches can cost a fortune. If you’re the proud owner of an ultra-fast home lab, you may have to drop thousands of dollars on a 10GbE PoE switch.
If you don't have one already, here are 5 reasons why you should arm your home lab with a dedicated network switch
Thankfully, there’s also a cheaper way to do things: if you don’t mind placing your switch near multiple power outlets and are willing to give up remote monitoring provisions for the IoT devices, PoE injectors might be more up your alley. Sure, they aren’t as feature-laden as PoE switches, but you won’t have to worry about blowing a hole in your wallet when buying PoE injectors.
Learn About Chemistry
Performing experiments in the laboratory require skills and perfection, I have composed a list of 50 chemistry lab equipment and their uses in the laboratory.
This is a guide on the list of lab pieces of equipment and their uses. This is the same as saying use of apparatus used in Chemistry.
There are different duties one could carry out in the chemistry laboratory and will certainly require specific lab equipment or apparatus. As a matter of fact, in Chemistry, we often take accurate measurements of mass, time, and temperature.
Mass is measured using Balance. A top pan balance measures in kilogram, it weighs chemicals in the laboratory to two decimal places
Temperature is usually measured using a thermometer. The thermometer reading should be taken when the thermometer is inserted into the liquid. The reading in degree should be to one-tenth of a degree accuracy.
Time is measured accurately using electronic stop clocks. They measure seconds to two decimal places.
For accurate and precise measurements, a specific apparatus may be needed. Your ability to deduce the apparatus that would give you accurate measurement is invaluable.
What is Accuracy? This is the closeness of a measurement to the actual value.
What is Precision? This is the closeness of measurements to each other.
This is the list of chemistry laboratory apparatus and their uses.
1. Evaporating dish : This is is usually made of porcelain to withstand high heat.
Uses : used for evaporation or heating a solution to dryness or saturation point.
2. Beaker : usually made of pyrex glass but some are actually made with plastics. It is cylindrical but has a lip for easy pouring of liquids.
Uses : used to hold solids or liquids during experiments n the laboratory.
3. Bell Jar : A cylindrical shaped apparatus made of thick glass.
Uses : used in combustion experiments
4. Burette : a long cylindrical glass tube with a tap or stop cock.
Uses : measures or delivers accurate volume of liquids up to 50 cm 3 .
5. Bunsen Burner : A metal tube with a wide metal base
Uses: A source of heat for experiments that require heating.
6. Crucible : made of porcelain and has a matching lid. It can withstand high temperatures.
Uses: It can withstand high temperatures and is usually used for heating substances until the
decompose.
7. Crucible Tongs : The apparatus is made of iron.
Uses: This is used for holding hot crucibles.
8. Desiccators : The apparatus is made of thick glass with a lid
Uses : used for drying and keeping dry solids.
10. Distillation Flask : This is a round bottom flask with a slanting long side arm.
Uses : used during simple distillation for the passage of the vapours into the condenser.
11. Conical Flask : This is a glassware apparatus with needle-like mouth.
Uses: used for holding or collecting liquids during experiments especially titration.
12. Filter Funnel : Can be made of glass or plastic with a needle–like bottom.
Uses: used during filtration and filling the burette
13. Gauze wire : made of iron mesh with the asbestos center.
Uses: Usually placed on tripod stand when heating to support the flask.
14 . Gas Jar: Made of glass with a flat glass cover.
Uses: used for collecting gases
15. Measuring cylinder : made of glass or plastic graduated and with a lip.
Uses: used to measure the volume of liquids but not accurately.
16. Gas Syringe : Laboratory equipment made of glass or plastic.
Uses: used to collect volume of gases during experiments in the laboratory.
17. Graduated Pipette : An apparatus made of glass or plastic
Uses: used to deliver accurately small volumes of liquids.
18. Bulb Pipette : glassware with needle-like ends
Uses: used to transfer accurately definite or specific volumes of liquids.
19. Dropping Pipette : An apparatus with a rubber teat.
Uses: used for dropwise addition of a solution or reagent.
20. Pipette Filler : made of flexible rubber .
Uses: it is used in filling the pipette with the solution or base.
21. Specimen tube or bottle : an apparatus made of glass or plastic.
Uses: This is used for keeping or storing a small amount of solids.
21. Spatula: A laboratory equipment made of plastic or steel that is chisel-shaped at the end.
Uses: it is used for transferring or putting small quantity of solids into test tubes or during
flame tests.
22. Deflagrating spoon : This is a long stainless steel wire with a cup at the end.
Uses: it is used in introducing small quantities of chemicals into the gas jar.
23. Retort Stand : a long cylindrical rod that can be coupled with a clamp.
Uses: it is used to support or hold burettes upright.
24. Burette Stand : This is usually a wooden apparatus used mainly during titration.
Uses: This is used to hold the burette uprightly and firmly during titration.
25. Test Tubes : This is a piece of apparatus made of glass sealed at one end.
Uses: used in qualitative analysis to hold reactants.
26. Test Tube holder : This piece of apparatus could be made of wood, brass, or stainless steel.
Uses: Commonly used to hold test tubes during experiments.
27. Thermometer : This is one of the very important chemistry lab equipment. It is made of glass with a bulb at one end.
Uses: it is used in measuring the temperature of liquid or solution.
28. Delivery Tube : it is made of glass and can be bent into any shape.
Uses: it is used to bubble a gas over a liquid or delivery gases into gas jar.
29. Tripod stand : An apparatus made of iron with usually three legs. It could bear a triangular or circular base.
Uses: usually used to support flasks when heating in experiments.
30. Pipette stands : This is a piece of apparatus made of wood or even plastic.
Uses: usually for keeping pipettes.
31. Capillary Tube : this is a laboratory apparatus made of tiny glass tubes with very small diameters.
Uses: applied in the determination of the melting point of solids.
The purity of a substance is determined by melting point, boiling point, and single spot on a chromatogram(for colored substances). Chemistry fact
32. Tile : this is an apparatus made of white plastic or tile.
Uses: used in titration for clear and sharp observation of colour change.
33. Pneumatic Trough: This is an apparatus made of thick glass that is cylindrical, rectangular but usually rimless.
34. Stopwatch : Very accurate timing apparatus
Uses: used in timing during experiments
35. Hofmann’s Voltametter : A glassware apparatus designed perfectly for the determination of water
Uses: used in the determination of the chemical composition of water
36. Watch glass : it is circular glassware with a round or flat bottom.
Uses: it is used for keeping solid you want to dry in air or desiccators.
37. Separating Funnel : A glassware apparatus with a short stem and stopcock.
Uses: used in separating immiscible liquids like oil and water.
38. Thistle Funnel : a glassware apparatus with a thistle head and a long stem.
Uses: used in experiments for intermittent addition of reagents.
39. Kipps Apparatus : A lab equipment made of thick glassware.
Uses: used in the intermittent supply of gases
40. Buchner Funnel : the apparatus is made of porcelain and has a fixed perforated plate.
Uses: it enables solids to be sucked dry and is also used for suction filtration.
41. Centrifuge : manual or electric operated machine.
Uses: used in separating solid particles in a liquid.
42. Leibig Condenser: made of glass tubes fixed together with openings for water inlet and water outlet.
Uses: it is used for cooling and condensing vapours into liquids. Usually used in distillation experiments
43. Combustion Boat/tube : usually made of aluminum and is boat-like in shape.
Uses: used in combustion experiments
44. Filter Pump: made of glass, plastic or nickel-plated brass.
Uses: it provides a Vacuum suitable for filtration by suction.
45. Flat bottom flask : A flask with a flat bottom base that can stand on its own.
Uses: it is used for boiling liquids in the laboratory.
46. Round bottom Flask : A flask made of glassware that has round bottom base.
47. Beehive Shelf : Made of porcelain or glassware with openings for insertion.
Uses: serves as a support for the gas jar during preparation and collection of gases over water.
48. Chromatographic jar or Tank : made of thick glass but rectangular in shape.
Uses: used in developing thin layer chromatographic plate.
49 . Cork : a wooden apparatus shaped with a matching cover.
Uses: for supporting round bottom flasks
Used in stoppers having one or two standard holes for connecting delivery tubes.
50. Water bath : made of metal and filled with water
Uses: it is used in gradual boiling and heating of liquids for slow evaporation.
These are the different laboratory apparatus fused for different specific uses.
I have also written an alternative version of this post, a tabular form of common apparatus used in chemistry,
Which is the Process by Which a Gas Changes to a Solid? Deposition, Evaporation, Freezing, Sublimation. The straight answer to this question is Deposition. Deposition is the change of state of matter from gaseous state straight to solid state without passing through the intermediate form which is liquid state. The summary of the processes that…
What is quantum chemistry? Quantum chemistry is the branch of theoretical chemistry that applies quantum mechanics to study the behavior and properties of sub-particles of an atom, especially the electron. What is an orbital? An orbital is a region where there is a high probability of finding an electron. There are basic principles that determine…
Stoichiometry problems involving mole to mole calculations by using balanced chemical equations to determine the amount of one substance (in moles) required to react with a certain amount of another substance (also in moles). In addition, every stoichiometry problem can be solved from the angle of mole-to-mole stoichiometry problem tips. In mole-to-mole stoichiometry, there is need to…
This is a complete guide to IGCSE alternative to practical chemistry and I have broken it down into several sections just to help us understand what is required in this section. Please remember in IGCSE Olevel chemistry, there are three sections. We have the essay(theory), objectives, and alternative to practical or Practical. The mark distribution…
Stoichiometry is a concept based on balanced chemical equation and stoichiometry can support the law of conservation of mass. We’ve discovered that in balanced chemical equation, the mass of reactants and products remain the same. What is law of conservation of mass? Law of conservation of mass is otherwise called the law of conservation of matter…
Resonance in Chemistry is otherwise called Mesomerism simply refers to the alternation or rotation of double bonds in some compounds which ensure their stability. Resonance in Chemistry is a term used to describe the representation of the covalent bonding in some compounds like Benzene, Carbon IV oxide, and even Ozone. Additionally, resonance exists in ions…
This is very educative and please I need more of this as this helps science students in many ways.
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A lab report conveys the aim, methods, results, and conclusions of a scientific experiment. The main purpose of a lab report is to demonstrate your
Read chapter 3 Laboratory Experiences and Student Learning: Laboratory experiences as a part of most U.S. high school science curricula have been taken fo...
General Considerations It is useful to note that effective scientific writing serves the same purpose that your lab report should. Good scientific writing explains: The goal (s) of your experiment How you performed the experiment The results you obtained Why these results are important While it's unlikely that you're going to win the Nobel Prize for your work in an undergraduate laboratory ...
2-give the necessary background for the scientific concept by telling what you know about it (the main references you can use are the lab manual, the textbook, lecture notes, and other sources recommended by the lab manual or lab instructor; in more advanced labs you may also be expected to cite the findings of previous scientific studies ...
Laboratory experiments can include animals as they offer greater experimental control opportunities than research with humans. ADVANTAGES: Lab experiments offer precise control over variables, minimizing extraneous influences and facilitating the establishment of cause-and-effect relationships, which is particularly advantageous in psychology ...
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.
You are already familiar with the steps of the scientific method from previous lab experiences. You will need to use your scientific method knowledge in today's lab in creating hypotheses for each experiment, devising a protocol to test your hypothesis, and analyzing the results.
12. Make sure to carefully read through the entire procedure before beginning an experiment in the lab. This will help prevent you from making mistakes that could compromise your safety. Notes: Since many laboratory procedures are carried over to the next week, make sure you bring previous lab write-ups with you to the following lab.
Abstract. Experimental protocols are key when planning, performing and publishing research in many disciplines, especially in relation to the reporting of materials and methods. However, they vary in their content, structure and associated data elements. This article presents a guideline for describing key content for reporting experimental ...
In this experiment, which will take two lab periods, you will use common glassware and equipment in order to study the physical property of density.
In this report, we provide insights into the replicability of laboratory experiments in economics. Our sample consists of all 18 between-subject laboratory experimental papers published in the American Economic Review and the Quarterly Journal of Economics between 2011 and 2014.
To demonstrate a capacity to utilize previous laboratory experiences to accurately interpret tests conducted to identify a certain organism. To know specifically which diagnostic tests are required to identify a bacterial species. To demonstrate skill in coordinating the usual laboratory work with that of identifying an unknown organism.
You can report a wildlife disease incident online or by calling the Game and Fish Wildlife Health Laboratory at 307-745-5865. Human cases are rare but precautions are warranted. If you have concerns that you may have come into contact with an anthrax-infected animal, please contact the Wyoming Department of Health and seek medical attention.
Meet your new never-take-me-off necklace. Prong-set with 17 lab-grown diamonds, this 14k gold necklace is designed with a bar shape that radiates light from all angles. The prong setting embraces the lab-grown diamond on a diagonal, allowing as much light to reflect through it as possible, so your jewelry sparkles all the brighter. Add it to your stacks for a touch of brilliance, or wear it ...
The suspension of "casework in the firearms and toolmarks section" of the lab commenced on Aug. 20, 2024, according to a news release issued by the lab. The suspension will remain in place prior ...
The Laboratory conducts world-class research that supports clean energy, a healthy planet, and solution-inspired discovery science. Berkeley Lab is defined by our deeply felt sense of stewardship, which we describe as a commitment to taking care of the Laboratory's research, people, and resources that are entrusted to us. Our values of team ...
8 Each day, before you leave your lab bench, clean off the bench surface. Remove matches and papers, and wipe down the surface with water and paper towels. C. EYE PROTECTION 1. You are required to wear approved eye protection in the laboratory whenever you are doing any experiment or whenever any experiment is being done in the laboratory around
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Classification Title: Enter the classification title here. Job Description: Dr. Artem Nemudryi's lab (nemudryi-lab.com) seeks a motivated Lab Technician to join our growing team in the Department of Biochemistry & Molecular Biology at the UF College of Medicine.Nemudryi lab uses CRISPR-guided ribonucleases to study how human cells repair RNA and how RNA viruses co-opt these mechanisms for ...
Assist the instructor or senior lab personnel in preparing lab experiments and demonstrations. Comply with all applicable health and safety regulations, policies, and established work practices. Maintain lab equipment by cleaning and performing basic repairs, contacting the supervisor for more complicated repairs.
Request PDF | How do different laboratory environments influence students' attitudes toward science courses and laboratories? | The science learning environment is an important factor in ...
Boston-based startup Galy says its found an alternative that avoids all of these problems by growing cotton in a lab. The company shared an evaluation by environmental consultancy Quantis to show that, at an industrial scale, its process reduces water use by 99 percent, land use by 97 percent and the negative impact of fertilisers by 91 percent ...
Rocket Lab USA (RKLB 4.62%) plans to go to Mars, and investors seem to think the stock could go along for the ride.. Shares of Rocket Lab climbed 19.7% in August, according to data provided by S&P ...
If you're the proud owner of an ultra-fast home lab, you may have to drop thousands of dollars on a 10GbE PoE switch. Related 5 reasons you should buy a network switch for your home lab
Performing experiments in the laboratory require skills and perfection, I have composes a list of 50 chemistry lab equipment and their uses in the laboratory.
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