Science topics: LawCivil LawWills
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Wills - Science topic

Legal documents that are declarations of individuals' wishes regarding the disposal of their property or estate after death; esp: written instruments, legally executed, by which dispositions are made of estates. LIVING WILLS are written declarations regarding prolongation of life by extraordinary means.
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I propose to conduct a study to assess youth's orientation towards Sustainable Development with specific reference to Triple Bottom Line in the Global South's Context, if scholars are willing to collaborate please feel free to combine effort and make a combined voice.
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Data and anayze it.
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Hello every one,
I am looking for the latest edition of the book '' Review of Forensic Medicine and Toxicology'' Including Clinical and pathological aspect for Gautam Biwas.
if anyone has access to it or is willing to share a copy, I would really appreciate your help.
Thank you in advanced
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i will share a soft copy of this book
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In your experience, which supply chain KPIs have had the most significant impact on improving business performance, and why?
(I am a final-year student at the South-Eastern Finland University of Applied Sciences (Xamk), studying in the Master of International Business program. I am currently working on my thesis, which focuses on Key Performance Indicators for Enhancing Supply Chain Performance.
I hope you will be willing to participate in my thesis.
All answers will be conducted completely anonymously, and the thesis will not reveal the identities of the participants. The organization will also remain anonymous in the research.
I would like to emphasize that participation is entirely voluntary. )
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Supply Chain Key Performance Indicators Depending on the industry, KPIs may vary. In many manufacturing companies, the main indicators are: on-time delivery, speed of delivery, quality of finished products, and productivity in the warehouse or in production.
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Dear colleagues,
I hope this message finds you well. I’m Dinesh Deckker, an early-career researcher with a growing interest in Artificial Intelligence. I am currently preparing to submit my first research paper to the cs.AI category on arXiv.
To proceed with the submission, I need an endorsement from a registered author in this area. If you're an endorser for cs.AI and are willing to support a new researcher, I would be truly grateful for your help.
You can endorse me by visiting the following link: 👉 https://arxiv.org/auth/endorse?x=SOBQOG Or alternatively, go to: http://arxiv.org/auth/endorse.php and enter the code: SOBQOG
I deeply appreciate your time and consideration. Your support would mean a lot as I take this important step in my research journey.
Warm regards, Dinesh Deckker
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Dinesh, I'm not familiar with arXiv, but I'll see if i can help.
-Best.
Victor
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I did the calculation previously where I optimised the reactant and product using b3lyp/6-31+g(d) followed by a refinement using b3lyp/6-311++g(d) and then ran a qst2 calculation at b3lyp/6-31+g(d) which worked, however I am required to use the B3LYP/aug-cc-pVTZ for optimisations, so I first optimsed the reactant and product using b3lyp/6-31+g(d) and then refined at B3LYP/aug-cc-pVTZ and when I ran the qst2 using these optimised structures I am getting the error: Old curvilinear step not converged, using linear step:
SCX= 2.13D+01 DXMaxT= 6.95-310 SCLim= 0.00D+00 Fact= 0.00D+00
RedCar/ORedCr failed for GTrans.
I dont think there is an issue with atoms not matching since I was sure they were and the qst2 worked using a different basis set. My current input is # opt=(calcfc,tight,qst2) freq b3lyp/6-31+g(d) nosymm scf=(qc,xqc,maxcyc=1024) however I also tried variants without xqc and variants with geom=connectivty and the error above still persists
I attached the log file if anyone may be willing to take a look, I would greatly appreciate help with this.
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Hallo, Joshua!
Your problem originates in geometries (sometimes small change in structure causes big problems). I have this type problem usually with rotation barriers.
In such case I use the 'qst3' keyword instead of the 'qst2' one. You can use the b3lyp/6-31g+(d) barrier structure as the 3rd geometry (=approximate barrier estimation).
Best wishes
mb
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"I am conducting research to determine whether a formula exists to systematically identify all possible addends (summands) that compose any given integer greater than two. By 'addends,' I refer to distinct sets of numbers that, when summed, equal the integer in question. For example, for the number 5, we get sets such as {1+4}, {2+3}, {1+1+3}, and so on.
I have already developed a formula that addresses this question, but I am reaching out to this esteemed community for additional perspectives. I would like to know if anyone can provide or suggest other formulas, insights, or approaches that tackle this problem effectively. I believe collaboration could enhance our understanding of the topic and perhaps reveal deeper implications in number theory or combinatorial mathematics.
I welcome any thoughts, references, or alternative formulas that you might be willing to share!"
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Dear Félix Oscar Socorro Márquez;
Thank you very much for sharing your valuable ideas on my created formula, your direct observation to my formula that it could systematically identify all possible addends is a very welcome development to my formula. Again thank you sir for your effort and time given to answer my question. Thank you in valuing research study like me.
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Would anyone be willing to participate in a short survey? Your insights would be invaluable!" If your age is from 18-25 years please do considered filling the form. https://docs.google.com/forms/d/e/1FAIpQLScHylBE32G3oWjDs_ufuniW8SBPAFu2PQ-eTbCkAniR08EoGQ/viewform?usp=header
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No estoy en el rango de edad. Mucho éxito.
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Can AI be considered a virtual processor? If so what is the purpose of old microcircuits other than being a part of a new integrated circuit?
I invite specialists to join the discussion
Im seeking to write an article based upon the theme Your ideas are welcome Open to suggestions and willing to coauthorship My email:
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AI can indeed be considered a virtual processor, particularly in the context of its architecture and functionality. The concept of virtualization in AI processors allows for the efficient sharing of resources among multiple users and applications, enabling enhanced performance and flexibility. This is evident in several key aspects discussed in the literature.
Resource Sharing and Virtualization
AI processors, such as those described in Hu et al., utilize a shared architecture where multiple users can access components like the Multiplier Unit (MXU) and Scalar Computing Unit (SCU) simultaneously, effectively functioning as a virtual processor(Yujie et al., 2019).
The implementation of a RISC-V core with simultaneous multithreading (SMT) allows for multiple threads to execute concurrently, optimizing resource usage and enhancing processing capabilities in a virtualized environment(Tanaka et al., 2022).
Compiler-Assisted Virtual Design
Huang et al. highlight the importance of a compiler-assisted virtual design platform that facilitates the co-optimization of AI software and hardware, demonstrating how virtual design tools can streamline the development of AI systems-on-chips (SoCs)(Huang et al., 2023).
This platform enables rapid functional verification and performance analysis, further supporting the notion of AI as a virtual processor by allowing for flexible design iterations.
Specialized Processing Capabilities
AI processors are equipped with specialized circuitry for tasks such as convolutional neural networks, which can be dynamically controlled to optimize processing based on input data characteristics(Mengqiu, 2019)(Kim et al., 2021). This adaptability is a hallmark of virtual processing.
While AI processors exhibit characteristics of virtual processors, it is essential to consider the limitations and challenges in their implementation, such as the complexity of hardware-software co-design and the need for efficient resource management. These factors can impact the overall effectiveness of AI as a virtual processor.
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Santa Cruz no longer carries the M20 glucocorticoid receptor antibody, which we are using to label a membrane GR. The G5 antibody that replaced it does not recognize the membrane receptor as well, so I'm inquiring as to whether there might be M20 available in the community that people are not using and willing to donate (or sell!) to us. Thanks.
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Hi Jeffrey,
If you urgently need an M20 glucocorticoid receptor antibody, the MCE Glucocorticoid Receptor alpha Antibody (HY-P80143) meets your requirements. The immunogen for this antibody is the full length of GRα of human origin, and it is suitable for Western blot (WB)
in both human and mouse samples.
Need Further Assistance? For detailed experimental protocols, purchasing information, or any inquiries, our team is here to help! Feel free to:
Our experts will respond promptly to support your research needs.
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Dear researchers,
If your expertise exists in conducting in silico molecular docking studies, please contact me to explore potential collaborations. I am working on a project that could greatly benefit from your expertise, and I am interested to discuss how we might work together to achieve our research goals.Thankd
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Please listen to Phil Geis - this is a reason for you article to be retracted and is highly unethical. I would suggest that you instead find a quality journal that does not have an APC or actually find out if you can publish for free as you are from a lower socioeconomic country. Do NOT risk your reputation and future on such a proposition that would shame you and your employer.
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Dear Colleagues,
All over the world, professionals just like ourselves are working hard to conduct research and explore new ways to share valuable information across the globe. I am a professor at Howard University College of Dentistry, in Washington, DC, USA, the Comprehensive Care Department and am cross trained in the Endodontics, Periodontics and Restorative departments. I have been a general dentist for 18 years and would like to collaborate with colleagues on a national basis, but more importantly, globally.
As I have conducted my research and written articles, having external reviewers is an essential part to our success in having our works published.
If you are interested in becoming a reviewer of my articles that are up for publication, please let me know at geetanjeli.sheogobin@howard.edu. Conversely, if you are in need of an external reviewer for any of your works, please do engage with me, as I am willing to collaborate with colleagues in the medical and dental fields in need of external reviewers of their research articles, reviews, and experiments.
I can furnish my curriculum vitae once your interest has been communicated to work internationally with myself and my student researchers. Please feel free to reach out to me at your earliest convenience.
Best Regards,
Dr. Geetanjeli R. Sheogobind, M.P.A.
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Dear Dr. Geetanjali,
I would be pleased to collaborate as a reviewer. I look forward to contributing.
Best regards,
Fabiola Pantigozo!
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I’m currently working on a project involving XRD analysis, and I was wondering if anyone here has access to the MDI DataScan software for XRD data acquisition and would be willing to share it for academic purposes. This tool would be incredibly helpful for processing and interpreting diffraction patterns, and I would greatly appreciate any assistance in obtaining it.
If you are able to provide the software or guide me on how to access it
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MDI (Materials Data Inc) was the developer of DataScan software many years ago. They are today probably best known for their Jade software for X-ray data analysis. The company was acquired a few years ago by the International Centre for Diffraction Data (ICDD) and is still based in Livermore CA. You can contact them directly - contact info on this webpage: https://www.materialsdata.com/#
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Dear Professors,Teachers and researchers,
I hope this message finds you well. My name is Sandeep Savitaprakash Sharma, and I am reaching out to you in my capacity as a researcher affiliated with JG Univeristy. I am conducting a research study aimed at understanding the Innovative pedagogies..
As part of this study, I kindly invite you to participate by filling out a brief Google form, which can be accessed via the following link:
Your input will be invaluable in helping me better understand Best Innovative pedagogies and teaching practices in education . The form should take no more than 8 minutes to complete, and your responses will be kept confidential.
If you are willing to participate, please fill out the form by 30th March 2025. Additionally, I would greatly appreciate it if you could circulate this invitation to other teachers who may be interested in participating.
This research has been approved by our University research ethicscommittee. If you have any questions or concerns, please do not hesitate to contact me.
Thank you for considering this invitation, and I look forward to your participation.
Best regards,
Sandeep Savitaprakash Sharma
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Best Innovative Pedagogy: A Blended Approach for 21st-Century Learning
Innovative pedagogy is essential for addressing the evolving needs of students in the 21st century, where critical thinking, problem-solving, collaboration, and digital literacy are crucial. Among the many pedagogical approaches, Blended Learning—a combination of traditional face-to-face teaching with digital and experiential learning—stands out as one of the most effective and flexible models. It integrates multiple innovative teaching strategies, ensuring that students receive a dynamic and personalized learning experience.
1. Blended Learning: The Best of Both Worlds
Blended learning combines in-person instruction with digital tools to create a more engaging and interactive learning environment. It allows students to learn at their own pace while benefiting from direct teacher guidance when needed. This approach is particularly effective in skill-based education, where active learning, technology integration, and real-world applications play a vital role.
2. Key Components of Blended Learning
  • Flipped Classroom: Students engage with learning materials (videos, readings) before class, allowing in-class time to be used for discussions, problem-solving, and collaborative projects.
  • Personalized Learning: Digital tools help tailor lessons to students' individual learning styles, ensuring that each student progresses at their own pace.
  • Project-Based Learning (PBL): Encourages students to work on real-world challenges, fostering critical thinking, teamwork, and creativity.
  • Gamification & Interactive Learning: Using elements of game design, such as badges, leaderboards, and challenges, to enhance motivation and engagement.
  • Collaborative & Social Learning: Online forums, peer discussions, and collaborative tools enhance student interaction beyond the classroom.
3. Why is Blended Learning the Best Innovative Pedagogy?
  • Enhances Engagement: The integration of technology (such as AI-powered learning platforms, simulations, and virtual reality) makes learning more interactive and engaging.
  • Increases Flexibility: Students have access to learning materials anytime, allowing for self-paced and differentiated instruction.
  • Promotes Active Learning: Rather than passively absorbing information, students engage in critical thinking, discussions, and hands-on activities.
  • Bridges Theory with Practice: Through project-based and experiential learning, students apply theoretical knowledge to real-world contexts, making learning more meaningful.
  • Prepares for Future Careers: With digital skills and problem-solving approaches embedded in blended learning, students develop competencies required for the modern workforce.
Conclusion
While no single pedagogy can be considered the absolute best in all contexts, Blended Learning provides a holistic, flexible, and student-centered approach that integrates the most effective educational innovations. It combines the benefits of traditional instruction, digital tools, and experiential learning, making it highly adaptable across different subjects, student needs, and educational levels. By implementing blended learning, educators can create dynamic and impactful learning experiences that prepare students for the challenges of the digital age.
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We would like to sponsor a special issue of Research in HRM on HR Analytics. However, we are not sure if scholars would be willing to submit manuscripts on the topic.
If we sponsored a special issue on HR Analytics, would you submit a paper on the topic?
Thanks, Dianna Stone
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Breaking barriers: driving HR analytics adoption in small and medium-sized enterprises
I have published a paper in this area. Its a growing field
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Good Morning,
I am currently looking for business organizations open to survey for my dissertation. I will be administering a short, electronic survey to draw conclusions about the correlation, if any, between a few leadership traits, organizational performance and follower commitment (employee retention). I need approximately 150 participant. Does anyone know of or have any experience with organizations willing to participat? I’ve reached out to a few nonpofits and a couple large organizations in the biopharmaceutical industry (I have experience in both) and have not received responses. I’m open to an industry.
Thank you to anyone who may share input!
Brianne
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I think you should approach companies directly. For instance, you can take appointments and convince them to research your desired topic. Most of the companies welcome appointments, so try that way.
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There are … a large number of the wives who remain uninterested in intercourse through the years of their marriage… (Alfred Kinsey)
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Do you have any research findings to support this assertion? If men wanted a more experienced woman, who understood her own needs so that she was satisfied more easily, surely they would find older women more attractive partners than younger women. Yet rich old men marry young models and many men leave their wives for a younger more amenable woman. Young women have less experience and are looking for a mate. Older women accept that sex is primarily a male pleasure. If they have financial security for their family, they do not need to keep pleasing men.
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I have been trying to utilize the whippr package in R to analyze VO2 kinetics, but am running into issues when I try to run the code with data from Parvo metabolic carts. When I run the sample data set everything works fine, but there appears to be some problem with reading the excel file. I have tried to format the data file numerous times but have had no luck. If anyone has experience with this and is willing to assist, please let me know.
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Whipp package analyzes gas exchange kinetics, modeling Parvo data to estimate parameters and understand oxygen uptake kinetics precisely and efficiently always.
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The question of the determinants of action remains a crucial point in understanding the genesis of adaptive and maladaptive behaviors (e.g., Buabang et al., 2024, in TICS).
A strict dichotomous approach to this issue suggests that with behavioral repetition in a stable context—due to lack of time, cognitive overload, or stress—so-called habitual behaviors take control of action, often to the detriment of valuation and response-selection processes that could otherwise give rise to more adaptive behaviors, such as moderating excessive alcohol consumption or curbing pathological gambling.
An alternative approach garners increasing interest: it posits that expectancy systems, which anticipate the effects of action, are predominant. Indeed, certain associations linking stimuli to behaviors facilitate the implementation or efficacy of goal-directed systems, which represent the default mode of our actions.
It is neither easy (nor perhaps possible) to prove this theory in a laboratory setting, but certain life experiences speak volumes. I will not delve into driving behavior, which, however, can be understood as being "in the service" of a goal to be achieved (e.g., arriving on time for a romantic date). Nor will I address those small, everyday habits that seem, on the surface, to indicate that certain routines are generated by default, supposedly to save cognitive resources better used for more noble tasks. Such instances, in my view, are anecdotal when weighed against the magnitude of the harm associated with what is deemed "bad" habits (e.g., addiction).
I would like to draw the reader's attention to certain processes that unequivocally characterize gamers of demanding video games. This is a recreational activity I am fond of, which can involve thousands of repetitive actions to automate highly complex action patterns. At the time of writing, I am preparing for the final boss in 'Sekiro: Shadows Die Twice'. I recently completed 'Elden Ring' and its New Game Plus, as well as the DLC 'Shadow of the Erdtree'. I do not consider myself an exceptional gamer, far from it, but through repetition and perseverance, I have succeeded.
In light of reflections on the contribution of automatic and deliberative systems, habits, and goal-directed behaviors—concepts I do not conflate, as goal-directed actions can be automatic—I wish to share some aspects of my gaming experience. The situation seems apparently clear: the general goal is to progress and understand the story, which requires defeating mini-bosses and bosses, as progression is otherwise impossible. More specific objectives also come into play, such as preparing the right equipment for each battle. However—and this is a crucial point—every gamer implores that action patterns become automated! This is essential for efficiently dodging or parrying attacks.
Indeed, gamers are highly motivated for their action patterns to become as automated as possible, requiring no conscious thought during combat phases. And the acquired action patterns can be complex. Indeed, it is not uncommon to realize that the habit of dodging an attack was not the right choice, particularly due to the low probability that the attack would be followed by a second, leaping strike. For gamers, the learned motor memory of action patterns is more probabilistic than it seems, due to the algorithms that determine opponents' behaviors. It explains why gamers often hope for "luck" during a fight, especially when familiar attack patterns are involved. In other words, habits are instrumental in achieving their goals. It is worth noting that modifying a poor combat habit is no easy task. These objectives are multifaceted: progressing through the story, of course, but above all, experiencing a sense of competence and mastery over a demanding sequence by entering a state of flow.
Comparison is not equivalence, but I imagine the described experience is akin to certain addictive behaviors: different goals are activated through mechanisms we are currently studying—namely, what drives individuals into action. As in addictions, a multitude of habits (underpinned by highly efficient and automatic calculation modes) facilitate goal attainment by serving the expected outcomes. While it may be tempting to "break habits" through methods that, let’s admit it, yield modest results, altering the goals to be achieved is no easier but far more promising.
In the anecdotal situation I briefly described—playing 'Sekiro'—it is quite possible that simply passing by my gaming computer triggered a desire to play, fueled by the hope of progressing in the story, feeling competent, and even aspiring to belong to the minority group of gamers who have completed the game (generally 20–30% of gamers). However, I would wager that if my computer were out of order, I would have found alternative ways to pursue these objectives, much like someone willing to make considerable efforts to obtain their drug.
In summary, let us not be mistaken, as it could waste our time: habits serve the goals to be achieved, not the other way around.
Something to ponder.
Xavier
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Dear Xavier,
"habits serve the goals to be achieved, not the other way around."
Pluralitas non est ponenda sine necessitas.
In any case, we should not overdo it.
Merci
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Hello, everyone. I am a research scholar in the Department of Chemistry at Jadavpur University. As enlisted in my bio, I worked on different research topics. Currently, I am working on the design and synthesis of MOFs and their applications. I had already synthesized a few numbers of MOFs and I can see their structure in the APEX software. I have only this small idea but can't finalize the CIF files for publication in the journals. hence I want to collaborate to fulfill my targets.
With due respect, it's my humble request to all of you, if you or anyone else is willing to help me, to do some collaborative work please put your valuable reply. It's urgent.
Thank you everyone for your valuable time.
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Currently I am looking for a crystallographer who will finalize my crystals for publication as a coauthor,
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Hello, has anyone resterilised fungal contaminated explants using H2O2 and had success? Would you be willing to share the protocol or have another method that successfully removes contaminants? Thank you in advance
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Yes, using hydrogen peroxide (H2O2) for sterilizing fungal-contaminated explants can be effective, as demonstrated in studies. A protocol that yielded success involved treating nodal explants with 5.5% H2O2 for 20 minutes, which achieved the highest sterilization rate (25%) while minimizing damage to the explants. However, higher concentrations or longer exposure times may negatively affect regeneration capabilities and viability.
If you are looking for alternative methods, consider using sodium hypochlorite (NaOCl) or adjusting pH levels during sterilization, as these have also shown effectiveness in reducing contamination while maintaining explant viability.
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In Iran, the role of small businesses on the economy and GDP is very significant. Therefore, the use of digital marketing in these businesses, given its many advantages, can be a powerful element that largely compensates for the shortcomings and limitations of these companies.
I am interested in topics related to the above sentences
I am willing to cooperate in researching the above topics.
Contact me
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Opt for collaborative digital marketing . For example The dealers or small manufacturers of a product or service set up a web portal where they display their products and offerings and the cost is shared by members
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May I know if there is any website that have free dataset of gravimetric method (ex: karl fischer titration) and spectra method?
It will be great if anyone willing to share their dataset.
Thanks
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You can find free datasets related to gravimetric and spectral methods on websites like Eigenvector Research, RamanSPy, Mendeley Data, and Nature, which offer various spectroscopic data for analysis. These resources provide valuable datasets for research and algorithm testing in analytical chemistry.
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I'm looking for the syngeneic cell line ENU1564 rat mammary adenocarcinoma cells. Does anyone have them, preferably in the USA, and are willing to share with me?
Thank you.
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Hi all,
Does anybody have this cell line (ENU1564)?
If yes, I hope you can share with us.
Thank you,
Mohammad
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I am interested to partake in researches targeted at aiding certain speech deficiencies. I have a passion in community work, and being a linguist, I will be willing to participate in works or projects that might require the assistance of an Applied phonologist who can assist speech impaired children. I am currently working on Tongue-tie, among children in Southern Nigeria. Keep me informed if there is any such research I can help out with.
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Thanks Eunice Kingsley mam. I want to answer the question in order to solve my assignment. So would you mind helping me to sort out this question's answer.
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in the field of Currently, I am studying and researching intensively in the field of spheroid, hydrogel and regenerative medicine, and I am willing to cooperate to do a review or research article. and hydrogel or regenerative
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Hello
Thank you for reaching out and expressing your interest in collaborating on a review or research article. Your focus on spheroids, hydrogels, and regenerative medicine aligns well with my research interests. I would be very interested in discussing potential collaboration opportunities with you. Please let me know how you would like to proceed, and we can set up a time to discuss this further. Looking forward to the possibility of working together.
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This question comes as regular teacher's want to remain in their COMFORT ZONE.. not willing to implement inclusive practices.. Like multisensory approach.. Differentiated instruction.. Cooperative learning.. Oeer tutoring etc.
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Sharmila Yadav Good question. Teachers' who do not want or not willing to take a step further in implementing any form of change like inclusive teaching methods because their students are used to the traditional lecture method (TLM) of teaching before they arrived in their classrooms. Even students are not welcoming to something different from TLM especially in higher education levels.
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Dear esteemed colleagues and professors,
I understand that this platform may not be the most appropriate place for this request, but as I was unsure of where to post this request where all respected professors and colleagues are present, I have decided to post it here.
I am a master's student in cellular and molecular biology and have been looking for a group or professor to collaborate with on writing a paper.
If you are willing and able to help, please send me message.
Thank you for your time and consideration.
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Hello everyone,
I have inherited an Olympus BX51WI microscope which I have used in the past. It is working normally except for one thing. I recently locked the pre-focus lock on the front of the microscope (see attached pictures) and now it is stuck in the locked position. I just can't get it unlocked without breaking it. Both fine and coarse focus works and everything is working well. Also this is not the first time I have locked the pre-focussing knob. It was working fine for a while. I don't hear any strange noises while the microscope is working.
Can any one help/have suggestions with this? Is there any way to troubleshoot this? Attaching a picture for reference.
Thank you!
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I think the grease might got old and sticky over the years. You might want to try a hairdryer to warm up the pre-focus lock. That will hopefully loosen the grease. Than you should be able to open the lock again.
Additionally, I had that problem with some vintage film photography lenses. When the grease is prewarmed and you are able to move the lock. Try to lock an unlock it several times, that should distribute the grease better and the results (for locking and unlocking) for the next month should be better.
Best wishes
Soenke
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Are there any professors working on AI, machine learning, or cybersecurity research who might be willing to include an enthusiastic student like me in their projects? I'm passionate about these fields and eager to contribute to ongoing research. How can I find professors who are open to mentoring students or including them in their work?
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Dear Haq Nawaz Malik Finding professors who are open to including enthusiastic students in their AI, ML, or Computer Science research can be a rewarding endeavor. Here are some steps you can take to identify and approach potential professors:
  1. University Websites: Visit the websites of universities known for their strong AI and ML programs. Look for faculty pages in the Computer Science or related departments. Professors often list their research interests, recent publications, and ongoing projects.
  2. Research Groups and Labs: Identify specific research groups or labs within universities that focus on AI and ML. These groups often have graduate students and faculty members who are actively seeking collaboration.
  3. Conferences and Workshops: Attend AI and ML conferences, workshops, or seminars. Networking at these events can help you meet professors and researchers who may be looking for students to assist with their projects.
  4. Social Media and Professional Networks: Use platforms like LinkedIn, ResearchGate, or Twitter to follow and connect with professors in the field. Engaging with their posts and sharing your interests can help you establish a connection.
  5. Email Outreach: Once you identify professors whose research aligns with your interests, consider reaching out via email. Introduce yourself, express your enthusiasm for their work, and inquire about potential opportunities to collaborate or assist in their research.
  6. University Research Programs: Some universities have formal programs for undergraduate or graduate students to engage in research. Check if your institution offers such programs and apply accordingly.
  7. Internships and Assistantships: Look for internships or research assistant positions that may be available in university labs or industry settings. These positions can provide valuable experience and connections.
  8. Networking with Peers: Talk to fellow students or alumni who may have connections with professors. They can provide insights or introductions that may lead to research opportunities.
By actively seeking out professors and demonstrating your enthusiasm and willingness to learn, you can increase your chances of finding a research opportunity in AI, ML, or Computer Science.
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Review and give advice
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I just read your paper. It was excellent. When I was getting my bachelor's in Special Education, I did clinical hours with a self-contained class consisting of 6-8th graders who had emotional behavioral disorder. They were great kids; the main problem I noted during my time there were major environmental disadvantages and adverse childhood experiences. I plan to take time to read the resources you cited because this is an excellent model. I did note a few mechanical edits, but nothing missing content wise. I noted that the paragraphs need to be indented, also the reference page needs a handing indent for each resource. The title for references needs to be centered as well. Here is an example of a handing indent reference page (literally just 2 random references I thought of right now lol. The shape of the references is what I am getting at.). Cheers on doing work to help other people.
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I want to submit a paper in this open access paid Q3 journal.
If someone is willing to be coauthor, then message me
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Are you inviting co-authors? Pls review my profile
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Hello everyone,
I'm currently conducting an academic research project on artists' books as part of my studies at the Institute of Creative Industries Design at National Cheng Kung University. I've created a survey to explore the factors that make these unique books captivating and engaging.
I would greatly appreciate it if you could take a few minutes to fill out the questionnaire. Your responses will provide valuable insights and greatly contribute to my research. Additionally, there may be a follow-up interview for those interested, so please provide your contact information if you're willing to participate.
Thank you so much for your help and support! If you have any questions or feedback, feel free to reach out to me.
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Why do you need the names of participants? And has this study been approved by the appropriate ethics review committee? It is an interesting topic.
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Good day, Everyone!
I hope this message finds you well. I am a third-year college student from Rizal Technological University, and I am reaching out to request assistance with the validation of our thesis titled "Effects of Enterprise Risk Management Practices on Financial Performance of SMEs".
I am looking for a qualified validator who possesses a Master's or Doctorate degree in Business Administration or Financial Management to review and provide feedback on our thesis instrument and questionnaire. If you meet the qualifications and are willing to assist me, I would be extremely grateful for your time and expertise.
Please let me know if you are interested by replying to this post or sending me a direct message.
Thank you in advance for your kind consideration.
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Good evening.
My name is Daniel, I'm studying for a doctorate in business administration with an emphasis on corporate finance. In addition, I worked for 4 years in the controllership sector in two small hospitals here in Brazil.
If you still need help evaluating the instruments, you can contact me via email (danielpabreu22@gmail.com).
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As the construction industry advances, the integration of Project Data Analytics and Artificial Intelligence (AI) is becoming increasingly crucial in project management. These technologies are essential for advancing Quality 4.0 by improving efficiency, accuracy, and decision-making processes. I am currently gathering data on these topics through a survey and seeking interviews with professionals in this field. Your collaboration would be highly valuable in supporting this research in any way you prefer. I have prepared a questionnaire and detailed written interview forms, and if you would be willing to participate in an online meeting, it would greatly support my work. Your expertise and input would be greatly appreciated.
Google Form Questionnaire: https://forms.gle/QXaDLBd9DYkS2tpP6
Interview Participation Form: https://forms.gle/PfQnML7Hofw8YvSh8
In-Depth Written Interview Form: https://forms.gle/7bSR29CrrucEdTZS6
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Project data analytics and AI play important role in advancing Quality 4.0 in construction project management. They enhance decision-making, optimize resources, and improve overall project performance. AI-powered tools can monitor construction sites in real time, identifying potential safety hazards and quality issues, which allows for immediate corrective actions.
Data analytics provides in-depth insights into site conditions, design materials, and resource allocation, helping to mitigate risks and ensure that projects stay on track. Furthermore, AI can automate repetitive tasks, improving productivity and reducing labor costs. These technologies collectively contribute to higher quality standards and more efficient project management in the construction industry.
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Do your questionnaire is open ended or on liberty scale.
1. If open ended, the number of items are too larges and if it is on liberty scale the number of Item is insufficient to define the variables.
2. Items/questions are large in lenght.
3. Have you did Item analysis?
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I kindly need five peer reviewers to review my Internal Medicine article in Cureus in order to publish it. (Cureus is a journal that requires the corresponding author to contact five peer reviewers in order to review the article before publication)
If you're willing to help with your feedback, please send me your Email, Full name, and Affiliation
Thank you so much in advance.
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I can review the article.
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Kao's panel cointegration tests , is there anyone willing to explain me the eviews-9 output for the Kao's panel cointegration tests?
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To apply the Kao Residual Cointegration Test in EViews:
  1. Open the workfile and create a group of the variables.
  2. Open the group window, go to View > Cointegration Test....
  3. Select Kao Residual Cointegration Test and configure settings.
  4. Run the test and interpret results.
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I have the Holtzman Inkblot Test Cards Form A, which I was able to purchase from an individual who had a set from 1958. I am now looking for Form B. I wish to do some research with this set of cards and cannot find them anywhere. If anyone has a set Form B I am willing to purchase them. My email is jspores@pnw.edu. Thank you.
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Yes, I would be interested in doing research with the Holtzman technique. Presently, I use the Rorschach Performance Assessment System® (R-PAS®), but was interested in determining if the Holtzman cards will provide superior reliability and validity. I am still search for Form B because I want to determine reliability of Forms A and B. Would you know anyone who has Form B?
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"Nuclear-mitochondrial DNA segments (NUMTs) are mitochondrial DNA (mtDNA) fragments that have been inserted into the nuclear genome." (Xue et al., 2023)
I would like to know under this definition, segments of NUMTs are inherited maternally for the offspring or they would be inherited from both sides of parents? Also, is there any impact if we use these loci to construct the phylogeny? Thanks for any information.
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Once the DNA segment has inserted itself into the nuclear DNA it evolves differently from the mtDNA in the cytoplasm of the female. Now in the nucleus, the NUMT is subject to the same recombination effects of any nuclear gene and to a different set of selective pressures.. It is the physical location of the mtDNA genes in the female cytoplasm of the egg that makes the mtDNA only maternally inherited. The sperm are little more than a nucleus. A NUMT would be incorporated into the sperm and the egg and therefore comes in two copies in the offspring.
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Anyone is working on Artificial Neural Networks (ANN) in research?? I am willing to learn about it is there any platform/workshop/course for free regarding the same!
Also I’m looking for this for a chemistry point of view
Thanks and Regards
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Ayushi Mishra I wouldn't mind in assisting you
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I am currently in the process of applying for HEC's IRSIP scholarship and am seeking assistance to connect with professors from top 200 foreign universities. My research interests revolve around Quality 4.0 and Industry 4.0.
Could you kindly provide guidance or possibly connect me with professors who might be willing to offer an invitation letter for my scholarship application?
Thank you in advance for your help and support.
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Yes, dear qamar you can email to the professors of my department here at USM-Malaysia. Its ranking is good and fall in top 150 world ranked universities.
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Hey there. I'm a Science, Business and Innovation student and for my thesis project I'm currently doing research on different production methods for large-scale cultivation of spirulina. Specifically, I'm comparing raceway ponds with tubular photobioreactors. The comparison I'm drawing is mostly techno-economic, but I'm also interested in comparisons in terms of product quality, sustainibility and reliability. As of right now, most of my research is based on literature and other scientific articles. I would love to validate some of my findings and hear what others think about large-scale spirulina production through interviews. So please, if you are willing to do an interview with me or know someone that might, let me know as it would help me greatly. Thank you in advance
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Hello, although I do not work with Spirulina, I have studies based on the production of C-phycocyanin with other isolates. If this information will help you, I can help you.
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I am presently working on a completed research entitled: "Improving the Vegetative Growth Response of Eggplants Using Organic Fertilizer with Effective Microbes and Laundry Waste Utilization Technology (OFEM-LUTech)" I am presently writing its publishable format. I am planning to include international collaborators / co-authors. Is it possible (ethical) to include in my manuscript an international collaborator / coauthors in the research I am working on. Their role specifically is to enhance the paper to be published. In exchange, they should also include me as a collaborator / co-author on their present research for publication, with a similar role to enhance your manuscript for publication, and other research-related tasks.
If this is possible and ethical, please recommend anyone, who are willing to collaborate with my research undertakings. I am hoping this will build partnership between my university and their Universities, and also for professional growth.
Let me know your thoughts on this potential collaboration.
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Thank you for your answer prof Luis. That's my dilemma, and thank you for your insight.
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Hello everyone,
I'm about to start my first research project for my dissertation, and I plan to utilise Q-methodology as my research method. However, I am encountering challenges in understanding how to conduct factor analysis and subsequently interpret the data. Despite watching numerous videos and reading several journals, I haven't been able to grasp it yet. As I have no prior experience with statistics or numerical analysis, this is entirely new to me.
Would anyone be willing to share their expertise and guide me through the factor analysis stage and data interpretation process?
I would be immensely grateful for any assistance provided.
Thank you sincerely for your time and support.
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You might take a look at the Sage "little green book," Q Methodology, by McKeown & Thomas.
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Hello,o o o o o o o o o
I have master's level training in logic and meta-logic, high marks, A's, but am not a practicing logician at all, I am a neo-empiricist pluralist (epistemic and ontological) who does not think any single CTM based model of the mind can be reduced to logic exactly because of a categorical ambiguity that gets contingently invoked.
Neurons appear and so must be first modelled as objects with endogenous functions rendered over many internal sub-relations describing their emergent dynamics (behaviour). BUT, when we swtich to building a bit model of human cognition in terms of neural patterns and inter-dynamics, especially when thinking of the brain as composed of neural bit maps made morphic to structures in reality "outside", we then need to categorize neurons on more purely exogenous and relational terms too.
I do not believe this is allowed (does not lead to wff's) in any model built over any singular, i.e. a strictly reduced and monist and singular classical logic based model, but I am not versed enough in these technical terms to be certain here about the argumentative or procedural complexities involved, and would welcome any logician's insights here (I am a "fan" of semi-classical model building, although!).
I am looking for a practiced logician, with expertise in Model Theory (building structures of interpretation) who might have a peripheral interest in philosophy of mind, but who is willing to consider non-classical approaches.
Quid pro quo!
If you want a primer on my overall concern with the limits of finalizing totalized logical models (TOE's), please give this a go:
Thanks, Brian
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I’m not much of a logician either, but it seems to me that given standard first-order logic, one can introduce an operator λx such that, when prefixed to an open sentence (predicate), creates a singular term for a property or relation. So for example given the open sentence Fx one can create λxFx to be a singular term naming the property of being F (or F-ness) and with the open sentence Hxy one can create λxyHxy as a name for the H-relation.
Then it’s business as usual:
Kermit likes the property of being green: LkλxGx
Kermit likes the relation of being to the right of: LkλxyRxy
The property of being tall, blonde, and not overweight is desirable. Dλx(Tx & Bx & ~Ox)
Parenthood is statutory: SλxyPxy
And the λ-terms can be quantified over just like the regular singular terms:
e.g. if SλxyPxy then ∃xSx
And you could quantify into the scope of the λ-operator too.
So basically you'd have a way of using singular terms as either unstructured objects or as displaying some internal relational features.
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...For research purposes to help others. If you are or know of anyone who is who would be willing to share his/her story, I would greatly appreciate the introduction! Thank you so much!!
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Yes. We have some melanoma survivors treated with immunotherapy for stage IV with 5 years of FU and remember now one patient with a remission of 10 years.
Immunotherapy and target treatments completely changed the future of metastatic melanoma.
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I am a master student at Erasmus university and writing my thesis about branding in the banking sector. I am desperately looking for participants for my interviews, a lot of companies are too busy and not willing to help. the interview can take place via teams or zoom, and would just take around 15 minutes.
I will ask some questions about what companies (from your perspective as employee) find more important in a bank, the transactional relationship and that the service is good, or a deep connection and bank that values the company and tries to inspire.
I am willing to share more about the subject, all help is appreciated!
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I was an ex-investment banker at ABN AMRO long back. if I qualify your search, please get in touch..
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Dear all,
Is there anyone willing to review (peer review) a research article titled: Engaging communities as partners in health crisis response: a realist-informed scoping review for research and policy?
If yes, I would need to have your full name and email address.
Thank you for your cooperation.
Mateus.
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Hello everyone!!! I am kindly willing to know your takes on this topic.
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Information and Communication Technology (ICT) can impact students' performance in a number of ways, both positive and negative. Here's a breakdown of the effects:
Positive Impacts
  • Enhanced Engagement and Learning: ICT can make learning more interactive and engaging through multimedia resources like videos, simulations, and games. This can lead to better understanding and information retention .
  • Self-Paced Learning: ICT allows students to learn at their own pace, revisiting concepts they struggle with and advancing when they grasp a topic.
  • Personalized Learning: Teachers can leverage ICT tools to tailor learning experiences to individual student needs and learning styles .
  • Collaboration and Communication: ICT facilitates collaboration among students on projects and discussions, fostering teamwork and communication skills .
  • Access to Information: Students have access to a vast amount of information and learning materials online, expanding their knowledge base beyond textbooks .
Negative Impacts
  • Distraction and Procrastination: Unstructured use of ICT can lead to distractions like social media or games, hindering focus and leading to procrastination .
  • Digital Divide: Unequal access to technology and the internet can disadvantage students from lower socioeconomic backgrounds .
  • ICT Addiction: Excessive use of ICT can become addictive, negatively impacting sleep, social interaction, and overall well-being, which can then affect academic performance .
Overall, ICT has the potential to significantly improve student performance when used strategically and effectively. It's important to find a balance and create a learning environment that leverages the strengths of ICT while mitigating the potential drawbacks.
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In my wife’s household, which she inherited from her mother-in-law, there is a hen that looks like a rooster, or a rooster that looks like a hen. For a whole year now we have not been able to determine whether it is a hen or a rooster. Probably trans or bisexual. How do you think?
Alexander
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Mother Nature is not always perfect. So, individuals (not breeds) may have imperfections such as both male and female characteristics.
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I kindly need five peer reviewers to review my Internal Medicine article in Cureus in order to publish it. If you're willing to help us with your feedback, please send me your Email, Full name, and Affiliation
Thank you so much in advance.
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Science involves challenging the status quo and being willing to ask difficult questions. Scientists need to be curious but also unbiased (not intent on proving any preconceived preferred result but open to accepting any conclusion that is supported by the evidence). There is no research that suggests that women are capable of the orgasms described in erotic fiction. Yet not even female sexologists are willing to discuss the issues that surround our understanding of women’s responsiveness.
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A new scientific truth does not triumph by convincing its opponents and making them see the light, but rather because its opponents eventually die, and a new generation grows up that is familiar with it.
Max Planck
And in your mentioned case Jane Elizabeth Thomas the commercial factor is also very strong to keep the status quo of accepted facts.
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I am willing to write and publish my work here on ResearchGate, how do I go about it.
Need your guidance.
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Please note that ResearchGate is not a publisher and not a journal, you cannot "publish" a paper here. It is a platform for papers published in journals, or to present unpublished texts, data etc. See also "Is ResearchGate a publisher?" in https://help.researchgate.net/hc/en-us/articles/14292596164753. And see this help page ("How to add research") for instructions how to add published or unpublished research to ResearchGate: https://help.researchgate.net/hc/en-us/articles/14293005132305
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If someone is willing to be coauthor in MDPI paper in management domain and pay APC, then you can message me
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I have published two papers in MDPI in 2023 and I will be happy to join you.
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Hello!
I would appreciatte any help finding sequence of plasmid pJ express 406 from extinct DNA2.0, I need to work with an inherited plasmid but information is missing.
Thanks in advance!
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Yannick Frey, Thank you for answering! I´ll defenitely do that.
Excellent day!
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What is the Ultimate Goal of Any Revolution?
Continuity until radical change occurs
Revolution is a type of violence.
Revolution has a beginning and an end.
Revolution has a beginning, like the Egyptian Revolution of 2011 and the French Revolution of 1789.
The French Revolution began on May 5, 1789, and continued until November 9, 1799.
It caused the abolition of absolute monarchy, established a secular democratic republic that became increasingly authoritarian and militaristic, radical social change based on liberalism and other enlightenment principles, the rise of Napoleon Bonaparte, and armed conflicts with other European countries.
As for the Egyptian revolution, it began on January 25, 2011. The repercussions of its events are continuing to the extent that its participants object to the lack of political freedoms, the state of emergency, the increase in poverty, the difficulty of finding job opportunities, police brutality, the lack of housing, the high cost of living, the rise in food prices, the spread of corruption, the lack of free and fair elections, and the lack of freedom of expression, poor living conditions, deviation from the path of truth, and the spread of falsehood.
The radical change has not taken place yet. The revolution is still alive within us and continuing till radical change is done if God Almighty wills. If God wills something, it will be done.
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I think regime change (or institutional change) is the ultimate goal of any revolution. Revolution is indeed violence, but violence is not necessarily bad and sometimes it is needed. For example, police is state-sanctioned violence and everybody agrees it is needed.
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Dear Professors, I need 8 Foreign panel members for my two Ph.D research scholars in the area of Graph theory in the subject of Mathematics. Willing professors will be in the position of Associate professor level in their Institution. Those who really interested in evaluating PhD thesis kindly send their updated resume to the mail.id hodpgmaths@stc.ac.in
I am expecting your consents and C.Vs.
Thank you everyone.
with warm regards,
Dr.O.V. Shanmuga Sundaram
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send their resume to hodpgmaths@stc.ac.in
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looking for researchers that are willing to work on discussion part and risk of bias of a systematic review, for more details pls leave a message
Thanks!
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I have sent you as message Arvind Kunadi
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Hello all. We are trying to get access to prostate cancer cell lines that were derived from patients who were Black or of African descent. There are numerous relevant cell lines reported in the literature, but they are hard to find for purchase - the only one we have found for sale is MDA PCa 2b / CRL-2422. Would anyone be able to provide a link to any others that are for purchase, or else be willing to share a flask or vial with us if you have some in your lab? We have reached out to some authors who developed relevant cell lines, but unfortunately haven't heard back yet.
Many thanks!
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Thank you very much! Yes, this is on our list (shared below) but unfortunately the only cell line out of these that we've been able to find available for purchase is MDA-PCa-2b. Do you know where we can get access to the cell line you mentioned?
  • MDA-PCa-2a
  • MDA-PCa-2b
  • P69SV40T
  • RC-77T/E
  • AA-103B
  • iHGPINc
  • S006AA
  • E006AA
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Hello,
I’m conducting market research on the management tools used by researchers to automate workflow, visualize processes, and manager budget & supply.
Anyone willing to address few questions in this regard, please connect.
Im interested in researchers all around the world!
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I agree with Dr. Qamar Ul Islam.
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Hello,
Can someone please provide me with some assistance? I am currently extracting RNA from human heart tissue using Omega Bio-Tek RNA kit I.
Here is a picture of some samples I did recently. Does anyone have any idea why samples C & D look like this and why I have no RIN ^e? Would anyone be willing to share the successful protocols they use also it is worth noting that the samples are already in a powder form that I achieved using liquid nitrogen to grind the tissue. Thank you!
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Did you treat your samples with DNase I? This might be gDNA contamination.
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We are about to start working on testing anti-protozoan agents against E. histolytica. I was curious if anyone had basic handling and culturing protocols they would be willing to share. I have been working on drug discovery targeting various human parasitic infections for 2 decades, but am new to e. histolytica. Have a bit of experience with giardia. Thanks in advance if anyone is willing to share some tested protocols!
Rob
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Hello there, curious researcher friend John Robert Gillespie! This is a fascinating field, and it's great to hear about your extensive experience in drug discovery.
Culturing E. histolytica can be a bit different from other parasites, so it's essential to follow established protocols carefully. Here's a basic guideline for culturing E. histolytica:
**Materials You'll Need:**
- E. histolytica strain (axenic culture)
- TYI-S-33 medium (Trypticase-yeast extract-iron-serum)
- Tissue culture flasks or tubes
- CO2 incubator (5% CO2)
- Sterile pipettes and culture dishes
- Microscope
**Steps:**
1. **Preparation of TYI-S-33 Medium:**
- Prepare the TYI-S-33 medium according to the specified recipe.
- Sterilize the medium by autoclaving.
- Once cooled, add a few drops of penicillin-streptomycin solution to prevent bacterial contamination.
2. **Inoculation:**
- Inoculate the E. histolytica strain into a fresh TYI-S-33 medium.
- Maintain the culture at 37°C in a CO2 incubator.
3. **Subculturing:**
- Subculture the amoebae every 2-3 days to maintain an actively growing culture.
- To subculture, harvest the amoebae by centrifugation, resuspend in fresh medium, and transfer to a new flask or tube.
4. **Monitoring:**
- Regularly monitor the culture for the presence of trophozoites and signs of contamination.
- Use a microscope to check for the typical appearance of E. histolytica trophozoites.
5. **Harvesting:**
- When you need to harvest the amoebae for experiments, allow them to grow to the desired density.
- Harvest the trophozoites by centrifugation and wash them with an appropriate buffer or medium for your experiments.
6. **Storage:**
- If needed, you can freeze E. histolytica trophozoites for long-term storage in liquid nitrogen or ultra-low temperature freezers.
Remember, maintaining a sterile environment is critical to avoid contamination. Also, note that E. histolytica can be potentially pathogenic, so follow appropriate safety protocols when working with this organism.
These are general guidelines, and the specific protocols may vary depending on the strain and the purpose of your experiments. I'd recommend consulting with colleagues or referring to the literature for more detailed protocols tailored to your specific needs. Good luck with your research!
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Good day!
I am a graduate student of MS in Civil Engineering major in Geotechnical Engg. Is anyone here have ongoing projects in the Philippines that has problematic soil and is looking for a geotechnical recommendation? This is for academic purposes only. Thank you
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While I don't have the capability to connect you with specific individuals or projects, I can offer some general advice on how you might find ongoing projects in the Philippines (or elsewhere) related to problematic soil conditions and geotechnical engineering.
  1. University Collaborations:Reach out to professors or researchers within your university or others who specialize in geotechnical engineering. They might be working on projects or have connections to industry professionals. Explore collaborative research opportunities that your department might have with industry players.
  2. Professional Networks:Engage with professional organizations or societies related to geotechnical engineering (e.g., the Philippine Geotechnical Society). Attend conferences, webinars, or workshops related to geotechnical engineering and establish connections with professionals and researchers.
  3. Government Projects:Explore government websites or contact local government units to learn about ongoing or upcoming infrastructure projects. Government projects often encounter geotechnical challenges and might be open to academic collaborations for problem-solving and research.
  4. Online Platforms:Join forums, groups, or online platforms related to geotechnical engineering and civil engineering. You might find individuals discussing their projects and challenges. Platforms like LinkedIn, ResearchGate, or specific forums might be beneficial. Engage in discussions, share your knowledge, and express your interest in collaborating on projects.
  5. Reach Out to Companies:Identify companies that work on geotechnical projects and send a polite, professional email explaining your academic interests and asking if there are opportunities to collaborate or learn more about their projects.
  6. Academic Databases:Explore academic databases and look for recent publications related to geotechnical challenges in the Philippines. You might find researchers who are actively working on relevant projects.
  7. Community Engagement:Sometimes local communities are aware of problematic areas, especially in rural or suburban regions. Engaging with communities might provide you insights into the real-world problems they are facing with regards to soil and geological issues.
Remember to approach each interaction with professionalism and a clear explanation of your academic intentions, objectives, and how you believe your involvement could be mutually beneficial. Best of luck with your research and academic endeavors!
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Hello to all.
My peers and I intend on using micro-CT scans to generate images of the penises of small mammals; in particular, we would like to assess the shape of the baculum (penis bone), glans and shaft of the penis. Although the process seems in general to be relatively straightfoward, part of our sample has gone through sweeping electronic microscopy (SEM) and is thus covered by a thin layer of metal, which can be platinum or gold, depending on the specimen.
My question is, is anyone familiar with any protocol for removing such metal layers from biological samples? Since we already have images of the soft tissue of the samples that went through SEM, we are willing to risk some damage to the soft-tissue layers of the biological sample; however, we need the baculum to remain intact within each penis.
P.S.: It has been pointed out by some colleagues that some acids may be able to remove the gold/platinum, but we are afraid that these will also damage the bone inside the penis to a greater extent than we are willing to risk.
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There are a few potential non-destructive methods for removing metal coatings from biological samples for electron microscopy:
  • This uses ionized gas (usually argon or oxygen) to gently sputter away surface contaminants. It can remove metal coatings while minimizing damage to delicate samples. The plasma power and duration need to be optimized to remove the coating but not etch the underlying sample.
  • Some chemical etchants like iodine or cyanide solutions can preferentially dissolve metal coatings faster than biological tissues. This may work for your purposes if the etch rate of the coating is much faster than the bone. Proper concentrations and etch times would need to be tested.
  • Applying a voltage in an electrolyte bath can cause the metal coating to oxidize and dissolve from the surface. Again, the voltage and solution composition can be tuned to selectively and gradually remove the coating.
  • Very gentle mechanical polishing with fine abrasives could potentially remove surface metal layers while keeping the overall structure intact. Though this runs a higher risk of damaging the sample.
The key for all these methods is controlling the rate and degree of metal removal to avoid over-etching the valuable biological structures underneath. I'd recommend starting with low concentrations and gentle plasma or chemical etching first. The goal is removing the minimum amount of coating required for analysis, without compromising the integrity of the soft tissues or bone
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Can we finally understand the world as it is? Does the world exist as it is?! Or has there always been a world with human events? A world that was not independent and was formed under the influence of human consciousness?! Until now, we have come a long way from the sensory boundaries of the world with scientific discoveries! Physical theories are so far from human senses that they bring to mind the same ideas of the unseen world! We have inherited the ashes of the explosion of a previous world, and after breaking the physical symmetries, we are busy identifying all the eras of this world in the pit of this world! This is a very strange situation!
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Consciousness theory ‘is pseudoscience’
A letter signed by 124 researchers claims that a prominent theory about consciousness — integrated information theory (IIT) — is “pseudoscience” because it cannot be empirically tested...
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I am willing to solve a problem concerned with flowing nanofluid particles in water as a Two-phase flow problem utilizing Comsol Multiphiscis within a 2D pipe exposed on its walls to a fixed heat flux. I am wondering which model to use for this problem? Should I use the Mixture model alone or the Non-isothermal mixture model? Any reply is highly appreciated. Moreover, if there is any available example, I will be grateful for that.
Regards,
Khalid
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Tonoy K. Mondal thanks again. But the previous paper about the non-isothermal mixture model in ANSYS FLUENT not COMSOL?
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Genes, Egg cell
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Yes, Correct
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I am using Terahertz time domain system to measure the thickness of a thin film on a substrate. I am able to calculate the thickness of substrate(~100um) alone. But what signs should I see for if there is a thin film ( ~100nm) on this substrate. I am not willing to do the fft ! Can time domain signal alone determines the thickness of film. The resolution is 33fs.
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When the terahertz pulse reflects off the top surface of the thin film and the bottom surface of the substrate, interference patterns can occur in the time-domain signal. These interference fringes are related to the film's thickness and the refractive indices of both the film and substrate.
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Does anyone have access to the following (quite old) article:
It would seems that I have no institutional access to it, and i was wondering if anyone would be willing to share.
Thanks
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I am trying to assess public perception of the veterinary profession and issues. I have prepared the questionnaires already and would need collaborators( who will double as coauthors) to look over the questionnaires and also help with the study design. I shall be collecting the data myself. If you are interested, please send me a message on gdogbey@uds.edu.gh
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Please can we have that discussion via email? Kindly furnish me with email address
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Science involves challenging the status quo and being willing to ask difficult questions. Scientists need to be curious but also unbiased (not intent on proving any preconceived preferred result but open to accepting any conclusion that is supported by the evidence). There is no research that suggests that women are capable of the orgasms described in erotic fiction. Yet not even female sexologists are willing to discuss the issues that surround our understanding of women’s responsiveness.
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Thanks Ghadah for your support! I really appreciate it. I am providing the research findings that are based on talking to women in the population. These findings have been ignored because they do not confirm male fantasies. I have found that many people find them helpful in understanding their relationships with the opposite sex.
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I am looking for advice from experienced individuals regarding the optimal conditions for plasmid electroporation in A375 cells. Would anyone be willing to share their expertise on this matter?
Additionally, I attempted electroporation using 140, 180, and 240 volts for both 70 ms and 35 ms, but unfortunately, the cells did not survive. Any suggestions on how to improve the outcomes would be greatly appreciated."
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thank you for your reply.
our lab just have BTX electroporator.
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Hi everyone!
I need to create the Beads task (by Jacoby et al.) using the OpenSesame software. Is there anyone who already has it and is willing to share it? I have permission from the authors to use the task but I'm struggling to create it using this particular software.
Thank you!
UPDATE: Thanks to a colleague from another lab, we will have the task soon (with task instructions in Serbian) and the experiment file for the OpenSesame will be publicly available.
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Hello, I am interested in the task. Is this available yet? Thank you,
ST
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Hello,
I hope this serious message "call for collaboration" could successfully reach the right professors and/ or funders, both in academic and industrial fields, who are really interested in the research area of "Biomass of Natural Fibers" and thier beneficial effect on a diversity of industrial engineering applications.
Recently, I was deeply involved in the mentioned research area and I have a particular contribution in a project closely related to that mentioned in the above title. To be comprehensive, I’m really willing to lead a research team or join a brilliant team by working under a leadership supervision of one of the esteemed professors in the mentioned research field. I will be so honered to transfer my experience earned from my latest successful project, and I’m sure that an aimful idea for establishing such a researching team work could be a very good step towards a prosperous future in making a multidesciplined progress in this research area and for opening many rooms for academics and indusrtial researchers who are interested in this field to have a prosperous future in thier career in line with the strategic sustainability development taking place worldwide and specifically in countries that are classified to be on popularized with thier agricultural development.
I’m willing to hear inspiring news and welcoming to any questions and feedback from all people who are interested in the idea by any way.
Best wishes,
Faithfully
Eyad Khalaf
PhD in Chemical Engineering, Polymer Composites
Agricultural Wastes Recycling & Sustainability
Tel.no.: +201001488248
Cairo, Egypt
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Dear Professor,
Below is a related article.
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intelligence is inherited but what about for indentical twins
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there mum
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hello, I'm doing research on ontology recommendations, I need an expert who can assess the results of my ontology recommendations. Is there anyone here who is willing to assess the results of the ontology recommendations that I proposed?
thank you for your attention
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Thanks for the recommendation
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Dear all,
I'm willing to perform a Linear Discriminant Analysis in Python using my own dataset. However the tutorials I find online only give examples of python's dataset. Can anyone please help me?
Kindly,
Cesar
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César António Mubango Hoguane Which is the data imput? You can compute it using nominal sieve openings and cumulative mass of material by using Linear Discriminant adopted from Sahu (1964). It is s a powerful method to determine sedimentation process.
Sahu, B. K. (1964) Depositional mechanisms from the size analysis of clastic sediments, Journal of Sedimentary Petrology, Vol. 34, No. 1, pp. 73-83.
med = the input is the given grain 'media'
des = the input is the given grain 'sorting'
ses = the input is the given grain 'skewness'
cur = the input is the given grain 'kurtosis'
Yab = (-3.5688 * med) + (3.7016 * des**2) - (2.0766 * ses) + (3.1135 * cur)
Ysa = (15.6534 * med) + (65.7091 * des**2) + (18.1071 * ses) + (18.5043 * cur)
Yds = (0.2852 * med) - (8.7604 * des**2) - (4.8932 * ses) + (0.0482 * cur)
Yft = (0.7215 * med) + (0.403 * des**2) + (6.7322 * ses) + (5.2927 * cur)
if Yab <= -2.7411:
Yab_eti = print('Yab_Aeolian deposition')
elif Yab > -2.7411:
Yab_eti = print('Yab_Beach environment')
if Ysa <= 65.3650:
Ysa_eti = print('Ysa_Beach deposition')
elif Ysa > 63.3650:
Ysa_eti = print('Ysa_Shallow agitated marine environment')
if Yds <= -7.419:
Yds_eti = print('Yds_Deltaic deposition')
elif Yds > -7.419:
Yds_eti = print('Yds_Shallow marine deposit')
if Yft <= 10:
Yft_eti = print('Yft_Fluvial environment')
elif Yft > 10:
Yft_eti = print('Yft_Turbidity environment')
The link bellow leads to a code that will provide the input variables for the sahu method: mean, sorting (standard deviation), skewness and kurtosis using the logarithmic method described by Folk and Ward (1957).
Folk, R.L., and Ward, W.C. (1957) Brazos River bar, a study in the significance of grainsize parameters, Journal of Sedimentary Petrology, Vol. 27, pp. 3- 26
for each sediment data collection point you can discriminate between different mechanisms and different deposition environments based on this method. But you can better automate the process in the language you want to generate the respective graphics.
Yours sincerely
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in accordance with islamic law
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نعم، حالات قد وضحها القانون القرآني، وتكفلت السنة بتفصيل الكثير من جزئياتها
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Over the past three years, I have been researching micro -scale enterprise market research practices, in the agri-food sector, in developing economies. In this regard I was looking for academics and /or practitioners who would be willing voluntarily to undergo a short one hour online interview. If in interest of supporting such a research, please leave a reply below or send a message over RG.
Thank you for your kind collaboration.
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Dear Martin,
Yes, I'm interested.
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Over the past three years, I have been researching micro -scale enterprise market research practices, in the agri-food sector, in developing economies. In this regard I was looking for academics and /or practitioners who would be willing voluntarily to undergo a short one hour online interview. If in interest of supporting such a research, please leave a reply below or send a message over RG.
Thank you for your kind collaboration.
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i am interestedsir.
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Hi, I am doing Ph.D. in electrical and electronics engineering, in Malaysia. I have completed my research. My research about (VANET Network). So I need to submit the external examiner's​ panel list to the university. Kindly suggest or if anyone is willing to be an examiner, please inform me and sent your details to my mail, The external examiner must have a professor from another state and an h-index higher than 20.
Thank you so much.
Regards,
Daniah Mohammed
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I advise you to check the profiles of various external examiners and choose the one that you think is appropriate to your thesis topic. You can check his publication as well, and then you may ask your supervisor for his advice.
Good Luck
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I am very confused as according to my reading, the name "Cephalosporium acremonium" is also similar to "Acremonium chrysogenum". Is it because it got reclassified? Because I seem to unable to find any relevant article and source that discuss this matter. Anyway I really need to clear this confusion for my assignment. Anyone willing to share their thoughts and knowledge with me?
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As a cognitive scientist, my expertise lies in the study of cognition and mental processes, rather than specific knowledge about fungal taxonomy or classification. However, I can provide some general information that may help clarify the confusion.
Taxonomy and classification of organisms can be complex, and species names can change over time as new information and research become available. It's possible that the name "Cephalosporium acremonium" has undergone reclassification or has been reclassified under a different name, such as "Acremonium chrysogenum."
Taxonomic changes can occur due to advancements in genetic analysis, morphological studies, or reevaluation of species relationships. Sometimes, as more research is conducted, scientists may discover that previously identified species are more closely related to other species or should be grouped differently within the classification system. These changes aim to reflect the most accurate understanding of the evolutionary relationships among organisms.
To obtain specific information about the classification of "Cephalosporium acremonium" and its relationship to "Acremonium chrysogenum," I recommend consulting reputable scientific sources such as taxonomic databases, research articles, or textbooks in the field of mycology (the study of fungi). These sources will provide detailed and up-to-date information on the taxonomy and classification of fungi.
Additionally, reaching out to experts in the field of mycology or microbiology may be beneficial in obtaining more specific and accurate information regarding the classification of these fungi.
It's important to note that the field of taxonomy is constantly evolving, and scientific names can change as new knowledge emerges. Therefore, it's always best to consult the most recent and reliable sources to ensure accurate information for your assignment.
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How can I delete a question from research gate
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Unfortunately I am veterinary surgeon and I use ready enjektabl stem stell cell solution
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I am looking out for an international collaborators. Thanks
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Interesting Apata Stella Bolanle - please keep me posted. Is this first-language/ second-language teaching? African languages or any language?
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Hi.
I am in the process of submitting a case report about Plasmacytoma (Gastroenterology) - Would anyone be willing to review it on Cureus? Thank you
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I could help you with this.
Thanks,
Ahmed
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Qualitative research is a methodology that I find incredibly interesting but also challenging in those aspects with which I am less familiar. I would like to propose that we have an area on ResearchGate where we can have ongoing dialogue on the topic, and include published and unpublished papers were have written. I would also suggest that we include audio and video examples of our research as well as discussions with such media. I have a presentation I made of qualitative methods at a seminary some years ago, which received very positive feedback from faculty and students. I would be willing to get the discussion started with videos of that presentation (which included audio and video data from my research) and related handouts. I tried to upload this to ResearchGate, and was not surprised when it was not posted. I made the mistake of sending it in a 1 gb zipped file, and not getting prior permission. But I could not determine how to get such permission until I saw this discussion area. Would you be interested in participating in such a forum?
Don Ratcliff, Ph.D.
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Unfortunately, it's not opening
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Inheritance represents the transmission of genetic features and their manifestation from one generation to the next. It's vital to remember that inherited features are handed on directly from parents to offspring, whereas heritable traits are not always genetic.
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  1. Inheritance: Inheritance refers to the passing of genetic information from parents to their offspring. It involves the transmission of genetic traits, such as physical characteristics or predispositions to certain diseases, from one generation to the next. Inheritance occurs through the transfer of genes, which are segments of DNA, from parent cells to offspring cells during reproduction.
  2. Heritability: Heritability is a statistical measure used in genetics and quantitative genetics to estimate the proportion of phenotypic variation (observable traits or characteristics) within a population that is due to genetic variation. It describes the extent to which differences in phenotypes can be attributed to genetic differences among individuals rather than environmental factors. Heritability is expressed as a value between 0 and 1, where 0 indicates that the variation is entirely due to environmental factors, and 1 indicates that the variation is entirely due to genetic factors.
Heritability does not directly measure the extent of genetic inheritance, but rather quantifies the contribution of genetic variation to phenotypic variation within a particular population. It provides an estimate of the relative importance of genetic and environmental factors in shaping the observed traits or characteristics.
To summarize, inheritance refers to the transmission of genetic information from parents to offspring, while heritability is a statistical measure that estimates the proportion of phenotypic variation within a population that is due to genetic variation.
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Hello, I am Willing to perform a QSAR analysis. Meanwhile, I have only 12 compounds in my library. On analysis, I found a good r2 value of 0.97 and s strong correlation diagram between experimental pIC50 and predicted pIC50. The problem is there's only one basis set for this number of compounds. Is it possible to include this analysis?
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Yes, it is possible to perform QSAR analysis for a dataset of 12 compounds. But, the statistical significance of the results may be limited due to the small number of compounds. It is generally advised to have a bigger dataset, ideally with at least 50-100 compounds, to improve the reliability and robustness of QSAR models.
In addition, the dataset needs to be diverse and reliable in terms of the chemical space. A small dataset might not include all of the structural and physicochemical characteristics required to build a trustworthy QSAR model. Therefore, it is crucial to carefully select the compounds in the dataset.
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Now several scRNA-seq platforms are used in Bacteria. I can not get the point.
Firstly, Bacteria have Horizontal inheritance, meaning they can exchange the genome. How to get the ref genomes in the mapping process? Is the heterogeneity due to horizontal inheritance or regulation or genome mutation?
Secondly, most scRNA-seq platforms analyze the Bacteria in the culture but not the original. What's the obstacle here? With culture, why not use bulk seq?
Thirdly, the RNA in Bacteria may be polycistronic mRNA, how to deal with them?
Why Not Single-Bacteria genome sequence?
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1. This reference genome can either be from the same strain of bacteria or from a closely related strain. In terms of the source of heterogeneity, it can be due to various factors, including genetic regulation, genomic mutations, and horizontal gene transfer. Horizontal gene transfer is not the only source of genomic diversity in bacteria. Regulation and genome mutations can also contribute to heterogeneity within a bacterial population. Single-cell sequencing of bacteria can provide insights into the heterogeneity at the level of individual cells and can help distinguish between these factors.
2. Culture vs. original sample: Many scRNA-seq platforms require the bacteria to be cultured in the laboratory before sequencing. This can introduce biases and may not reflect the natural state of the bacteria in their original environment. In some cases, it may be possible to perform single-cell sequencing directly on environmental samples, but this can be technically challenging and may require specialized methods. Bulk sequencing can also be used to study bacterial communities without the need for single-cell isolation.
3. Polycistronic mRNA is a type of mRNA molecule that contains multiple coding regions, each encoding a different protein. These regions are separated by non-coding regions called intergenic regions. There are methods that can help to address this issue of polycistronic mRNA, such as using barcoding or unique molecular identifiers (UMIs) to label individual transcripts.
4. Single-bacteria genome sequencing can provide valuable information about the genetic makeup of individual bacteria, but it may not be suitable for all research questions.
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Just about everyone these days uses fossils to calibrate molecular divergence. Fossils only provide minimum ages, but these are magically transmogrified into actual or maximal dates that are supposed to falsify earlier origins supported by tectonic methods. Ancestral area analysis can generate chance dispersal for patterns that could just as well be the result of vicariance. Ancestral area analysis uses areas that have no emperical existence. Its all a bit like following Alice down the rabbit hole. Numbers or not, nonsense is still nonsense.
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Andrew Paul McKenzie Pegman Exactly! At least you are not a practitioner of the methods. But there are plenty who are (and tons of funding) and I was interested to see if anyone out there might try to defend what I view as nonsense (because of the issues outlined). Its indefensibility may be why some prominent NZ practitioners chose to call of suppression of competing research programs rather than provide effective defense of their own.
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Please share your thoughts.
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You are most welcome
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Is there any systematic way approach to to analyze the I-t curve obtained from chronoamperometric deposition for beginners? Such as,
how to obtain the values of a and b which is instantaneous and progressive nucleation & growth? I am willing to understand 2 dimensional/3 dimensional growth.
Kindly help me , I am new to this topic.
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Analyzing the I-t curve obtained from chronoamperometric deposition can be a complex task, especially for beginners. Here are some steps you can take to analyze the curve and obtain the values of a and b for instantaneous and progressive nucleation and growth:
  1. Plot the I-t curve: Plot the current (I) vs time (t) curve obtained from chronoamperometric deposition. This curve will show you the behavior of the deposition process over time.
  2. Identify the different regions: Identify the different regions of the I-t curve. There may be a nucleation region, a growth region, and a steady-state region. Each region will have different characteristics that you can use to determine the values of a and b.
  3. Determine the nucleation region: The nucleation region is the initial region of the curve where the current rapidly increases due to the formation of nuclei. In this region, the value of a can be obtained by plotting the logarithm of the current vs. time and determining the slope of the linear region.
  4. Determine the growth region: The growth region is the region where the current gradually increases due to the growth of the nuclei. In this region, the value of b can be obtained by plotting the inverse of the current vs. time and determining the slope of the linear region.
  5. Consider 2D or 3D growth: If you want to analyze 2D or 3D growth, you can use different models to fit the I-t curve. For example, the Avrami-Erofeev model can be used to analyze 2D growth, while the Kolmogorov-Johnson-Mehl-Avrami model can be used to analyze 3D growth.
  6. Validate your results: Finally, it is important to validate your results by comparing them to theoretical models or experimental data from other sources. This will help ensure that your analysis is accurate and reliable.
Overall, the key to analyzing the I-t curve obtained from chronoamperometric deposition is to understand the different regions of the curve and how to determine the values of a and b for each region. With practice and experience, you can become more proficient at analyzing these curves and obtaining meaningful results.
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I am working on finding out the customer base who would be interested in taking the airplane between two Norwegian cities (Førde and Bergen). Driving by car takes at least 3 hours, and by bus around 3,5 hours. Driving by train or boat are not options. Interviewees representing various businesses tell that they would be willing to take the airplane (30 mins + some waiting, etc.) to save time for work related purposes.
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This is a fuzzy-logic question: that is, there is not one solution. Some people would drive for 6 hours rather than a half-hour flight. The choice is not just time but ease of travel and, of course, preferences. What is most important is to have the choice, there are too many people who think that rights should be curtailed to match their beliefs.
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In the Egyptian language, the term "God willing" has a different concept than in the West. This means that it will never happen in the life of our planet.
If I am lucky enough to understand the introduction to the theory of everything, I can assume that it cannot be completed during the lifetime of our planet, and therefore there will be no end to physics or math.
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The theory of everything is like infinity. You can aim in the general direction, but you can't get there from here, because there is no THERE to get to.
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Do you think "gene" is a program? Do they look like programs that creatures inherited from the previous generation? Like a solidified program in a computer chip? Why does biology not see "genes" as programs? If the gene is the program, you can treat the gene as a continuous sequence. Now biology knows that many genes work together, but it doesn't seem to focus on the order of the genes yet, and I don't know much about biology.
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It gives a set of instructions for how a "dish", namely the organism, is to be prepared. More linear than a program.
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Why does it take so much time to review a paper?
From my humble experience as an editor of a top tier journal, i can tell you its the editor’s lack of effort. in general. People should only volunteer if they have and willing to give enough time to find proper reviewers and review.
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This depends on many factors such as the resources available, the type of journal (we know that OA journals are faster), the average response time of the journal (reviewers included) and, of course, the fit of the manuscript with the editorial line.
With a colleague, we submitted an article that has been under review for a year now. It's coming along. I suggest you write to the editor to get a clearer picture of the situation...
Regards,