Stem-Tober 2023 | Cereal or a Rock?

StemComm’s Fall 2023 event was Stem-tober Block Party! We invited everyone to join us for a fun evening with science-based activities, prizes, and more! We had our event near where the physics students have their annual pumpkin drop. 

Ideation & Brainstorming: 

In the ideation process, we split into groups to come up with some ideas for what we wanted our fall event to be. We came up with over 10 ideas. To narrow them, I made a google form that had everyone rank their top 3 choices. After looking at the results, we decided on these activities:

Group 1: Liquid Nitrogen Ice Cream and dragons Breath Candy

Group 2: Gene-Tic-Tax

Group 3: Dragon’s Beard Candy

Preparation:

I was part of Group 1, so we got together and discussed what some of the materials were required. We originally wanted to do ice cream, so we made this list:

  • Materials Needed for Ice Cream
    • Liquid Nitrogen from Chem Department
    • Gloves
    • Ice Cream Base
      • Milk (4 cups)
        • Oat milk
      • Sugar (1 cup)
      • Vanilla extract (1 teaspoon)
      • Corn Starch (3 tablespoons plus 2 teaspoons)
    • Metal Bowl (large)
    • Hand mixer

We quickly decided not to do the liquid nitrogen ice cream and to just focus on the dragons breath candy because it would be easier to make as people came up to our table.

We had some options as to what we wanted to dip into the liquid nitrogen that would give participants “dragon breath.” We were thinking of dipping cereal, so we requested to order large spherical cereal, but it wasn’t going to come on time, so we ordered regular Fruit Loops and marshmallows instead. We also ordered bamboo skewers and contacted a professor to get access to liquid nitrogen canisters. 

The last thing we had to get ready was our poster. We had a poster designed on Figma with a fun dragon and fire visual. We also had some more informational posters that would describe what liquid nitrogen was and how we were using it in our experiment demonstration. 

Day of the Event:

Before the event, I went to the library to print out the poster. After, I met up with all the StemComm people near the Howey building where our event was taking place and helped set up the table, liquid nitrogen setup, and posters. It was a little slow in the beginning, some people who came up to our table were just students passing by, or people who were trickling in for the Pumpkin Drop event. Soon, more people pulled up to our event and we were dipping cereal in liquid nitrogen to give to as many people as we could. 

It was really fun to see people’s reactions to the texture, taste, and density of the liquid nitrogen-dipped cereal. After trying it myself, I found the cereal to be almost the same density as a rock. It was tougher to bite on and made a really big crunch sound. 

If I could change one thing about what we did for the event, it would be make it more apparent that the usage of liquid nitrogen can be hazardous and to partake in our activity at your own risk.

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  Timothy Durham was convicted of rape when a test showed his DNA genotype matched the DNA recovered from the crime scene. Eye witnesses testified that Durham was in a different state at the time of the incident, but he wasn’t exonerated from his 3000 year sentence until follow up DNA analysis showed that the preliminary forensic analysis used in the trial was misinterpreted (Thomas et al.). DNA testing serves an invaluable part in our criminal justice system, but it comes with complications and bias that can lead to wrongful convictions and misinformed juries.  

Background:

Forensic genetics aims to identify the origin of a biological sample. It can be traced back to Karl Landsteiner who discovered human ABO blood groups. With blood groups, suspects could be eliminated based on their blood type. For example, if a suspect had type A blood and there was type B blood left at the scene by the perpetrator, the investigators could rule out the suspect. Unfortunately, the reverse didn’t work. If the suspect and perpetrator both had the same blood type, it can’t be concluded that the suspect was guilty. Blood identifiers evolved into 8 distinct categories which improved the ability to eliminate suspects, but could only conclude that (if the system matched) it might be the perpetrator or this person might be related to the perpetrator (Jobling and Gill). The field evolved in the 1980s with the discovery of Minisatellites, lines of repetitive DNA that don’t encode proteins. Minisatellite patterns in DNA create what we know today as the DNA fingerprint, and it has a much higher accuracy rate than previous methods (Augustyn et al.). Around the same time, a breakthrough for victims of sexual assault was discovered. In the case of assault, bodily fluids of both the victim and the assaulter can get mixed. A process called differential lysis was created which could selectively increase the concentration of sperm in a fluid sample thereby allowing for accurate DNA testing (Jobling and Gill). Forensics evolved to use single-locus probe testing after several years because of its ease of interpretation. It looked at specific minisatellites that had high variability between subjects. This was the first DNA-based method to be used in a criminal investigation. Two murder homicides from several years apart were connected using DNA evidence. The evidence was then used to exonerate an innocent man, and the guilty party was found when he tried to evade mandatory DNA testing for all men in the small town. His guilt was then reinforced when the DNA profiles matched, and he gave a confession (Jobling and Gill). Finding DNA at a crime scene doesn’t guarantee that you’ll find a murderer. There are issues with non-pure samples and limited samples that make DNA work difficult, and accreditation of facilities and new techniques and take time (Jobling and Gill).  

Subjectivity of DNA Interpretation:

In a 2009 publication, the National Academy of Science discusses the possibility for subjective influence in lab based forensics. The interpretation bias happens in complex cases where, for example, there could be a mixture of DNA. A study published in 2011 looked specifically at this issue. A gang rape happened in Georgia, and the mixture in DNA from the case was used to prosecute one suspect after another suspect took a plea bargain to testify against him. With DNA mixtures, there are three possible conclusions: suspect excluded, suspect cannot be excluded, and inconclusive. If the suspect is excluded, it means that there’s little to no possibility that his DNA is part of the sample. If the suspect cannot be excluded, it means that there’s a possibility that his DNA is part of the sample. In the trial, the DNA examiners who knew the context of the case concluded that the suspect being prosecuted could not be excluded. The 2011 study gave the DNA evidence from this case and the DNA profiles of the suspects to 17 forensic examiners. These examiners had no context of the case, and they all worked independently. Of the 17, only 1 came to the same conclusion (suspect cannot be excluded) as the examiners who knew the context of the case. Twelve of the 17 concluded that the suspect who was prosecuted and convicted had no relation to the DNA found in the sample. Not only does this show that subjectivity occurs due to the context of the case, but the 17 examiners came up with different findings based on their past experiences meaning that not all DNA analysis is objective. Some organizations like the Scientific Working Group on DNA Analysis Methods say that quantitative statistical evidence should be presented with every categorical conclusion, but the US doesn’t require this (Dror and Hampikian).

False Positives:

There are two categories that cause wrongful identification in a DNA report: coincidental matches and false positives. Coincidental matches are DNA matches between two unrelated people. The probability of these matches is about 1 to 500,000 for white individuals and about 1 to 350,000 for black individuals. This small probability of coincidental matches makes people feel confident in DNA evidence. False positives, on the other hand, are matches between DNA and test DNA that result from issues in the forensics lab. There have been multiple cases of forensics labs accidentally switching victim and suspected rapist DNA which lead to convictions that were later overturned when the lab realized the error. There are also cases of misreading or misunderstanding a sample. In a case from 1993, a man was convicted of rape because someone interpreted a mixed sample of victim and perpetrator DNA as an individual sample. The conviction was again overturned. To prevent false convictions, retesting DNA is allowed, but it’s not an efficient solution. Many people are pushing for statistical information on the probability of false positives, so that the jurors can make accurate judgements based on DNA evidence (Thomas et al.).  

Conclusion:

DNA analysis is a useful tool for the criminal justice system, but subjectivity can be an issue in forensic testing. To combat wrongful convictions, there are organizations like The Innocence Project who use DNA testing to free the innocent, but reformed forensic testing standards should be put in place to prevent subjectivity and to ensure juries are correctly informed during trials. https://www.innocenceproject.org/    

Citation:

Augustyn , Adam, et al. “DNA Finerprinting.” Encyclopedia Britannica , 26 Apr. 2018, www.britannica.com/science/DNA-fingerprinting#ref153186. Dror, Itiel E., and Greg Hampikian. “Subjectivity and Bias in Forensic DNA Mixture Interpretation.” Science & Justice, vol. 51, no. 4, 2011, pp. 204–208., doi:10.1016/j.scijus.2011.08.004. Jobling, Mark A., and Peter Gill. “Encoded Evidence: DNA in Forensic Analysis.” Nature Reviews: Genetics, vol. 5, no. 10, Oct. 2004, pp. 739–751., doi:10.1038/nrg1455. Thompson, William C, et al. “How the Probability of a False Positive Affects the Value of DNA Evidence.” Journal of Forensic Sciences, vol. 48, no. 1, Jan. 2003, pp. 1–8., doi:10.1520/jfs2001171.