As an undergraduate, I was encouraged by my teachers in high school to volunteer for a professor to help with one of their research projects. Since professors are usually juggling classes and research, many of them need the manpower. I decided to volunteer for my professor Dr. Chris Lobban (now retired as a professor) who had taught me for biodiversity photomicroscopy and scientific writing. Because a portion of one of our classes had to do with microscopy, I would visit him at his office to have a nice chat and I inquired one day at the end of a semester if he was looking for volunteers. And so began my dazzling diatom experience into the world of microscopy. I didn’t know it then, but that was some golden advice I was given.
One of Dr. Lobban’s long term research projects was the Western Pacific Diatoms Project. He was one of the experts of marine and aquatic diatoms but lacked the time to work through all his carefully dated and labeled slides from numerous locations throughout Guam and the Marianas. I set to work on a bunch of slides from Guam as well as Saipan (since I’m from there, he thought it would interest me more). I was already familiar with handling a LM from my undergrad studies, but the cool thing about his microscopes at the lab in House 28 (his research space) was that the microscopes also had a camera and could take photos. There were 2 ways to go through a slide, he explained to me. One way was to zigzag randomly everywhere, covering as much of the slide as I could. The other way, was perhaps more time consuming, but more thorough, and that was to begin from a corner and work your way systematically to the opposite corner on the other side of the slide, overlapping slightly so you can get EVERYTHING (I usually began at the top left and ended at the bottom right). I am a much more systematic than random person, so I chose this method. Every time I took a photo, I had to note down the location of the slide as well (going by the ruler on the side of the microscope) and as he was looking through the photos I took he would attempt to locate the ones of diatoms of interest. We made progress.
In addition to my LM microscopy, Dr. Lobban also taught me how he went about mounting the slides he used for his high-powered Phenom scanning electron microscope (SEM), which used a beam of electrons to form images at a higher magnification than any other microscope I’d seen or used before. I was amazed at how many steps it took to get to a finished, mounted stub, but was grateful that he shared his process with me. As a first mentoring experience, Dr. Lobban took care in teaching me his approach to the scientific method and his philosophy on research, which I loved. He also discussed my career goals with me at the end of a few of our microscopy sessions over a mug of hot chamomile herbal tea. I truly felt at home performing the research and having something meaningful to contribute my time to. Although I spent much more time on the LM, we did go through a few stubs with the Phenom, though I preferred not to use it without Dr. Lobban in the lab in case I made a costly mistake. Costly mistakes are not what I wanted to make this early in my research career.
I continued to visit House 28 in my spare time between classes as a freshman and sophomore, but before the beginning of my junior year I had to turn the keys over to the beloved House as I was now juggling school and a job, which left little time to contribute to any research. Dr. Lobban e-mailed me not long after I turned in the keys with a link to his published manuscript, including me in the acknowledgements along with his other student researchers. I was happy to read that he described many new kinds of diatoms in his paper. I was, and am, extremely thankful to have had this as my first long-term volunteer research experience. It led to many doors being opened later, though I wasn’t aware of it at the time.

