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NESM Spring Symposium

Friday, April 25 2025

NESM is pleased to announce that this year's Spring Symposium will be held virtually and free to attend.

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We have an exciting program of speakers and career panels lined up. Interested in giving a talk? We have opportunities for research and vendor talks at this symposium. Make sure to submit your abstract no later than 10 April 2025! Register by clicking the button below and then you will be sent an email to submit your abstract!

Registration

Register now to attend the virtual meeting. Make sure to submit an abstract to be considered for a presentation! Not a member yet? Join for free here.

Vendors may also register for a 10-minute flash talk. Please contact us if you have any questions about registration or presenting at the symposium.

Schedule at a Glance

Friday, April 25 2025

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9 am

9:15 am

10 am 

10:15 am

10:30 am 

10:45 am

12 pm

1 pm 

1:50 pm

2:05 pm

2:15 pm 

2:30 pm

 

3:00 pm

3:50 pm

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Welcome from the NESM Board

Keynote - Edward Vicenzi

Speaker 1

[Coffee Break]

Speaker 2

Microscopy Career Panel

[Lunch Break]

Vendor Flash Talks

Speaker 3

[Coffee Break]

Speaker 4

Virtual Core Facility Tours
      Joerg Nikolaus -Yale West Campus Light Microscopy
      Sarah Sterling - MIT CryoEM Facility @ MIT.nano

Keynote - Katrina Velle

Closing Remarks

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Keynote Speakers

We are pleased to announce our two keynote speakers for this year's symposium.

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Museum Conservation Institute

Smithsonian Institution

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UMass Dartmouth

Panelists

Interested in a career in microscopy? Join us to hear from scientists in industry, government and academia!

Session Moderator: Emma Perry (University of Maine)

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Massachusetts Life Science Center

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Boston Police Department

Precious Stone

Oxford Instruments Andor

Chalcopyrite Rock

Harvard Medical School

Edward Vicenzi
Museum Conservation Institute
Smithsonian Institution

Bio​

Edward Vicenzi is a research scientist at the Smithsonian Institution’s Museum Conservation Institute. His work involves using microscopy and microanalysis to study museum specimens and related materials to understand their origin and history.  Before taking up his position at MCI he served as the Director of the Analytical Laboratories in the National Museum of Natural History’s Department of Mineral Sciences, and prior to that was the co-manager of the Imaging and Analysis Center at Princeton University. He has served as President of both the Microanalysis Society and the International Union of Microbeam Analysis Societies. He is currently an editor for the journal Microscopy and Microanalysis, on the editorial board of npj Heritage Science, and is a Fellow of the Microanalysis Society.

Abstract

Milli- to Nano-scale Examination of Early Metal-based Photographs

 

Following the invention of photography in 1839 in France, the daguerreotype technique caught on with a handful of experimentalists in the United States. Like the initial phases after many new discoveries, methodologies were in flux during those first years, and the materials used were not yet standardized. A small, dedicated team of Smithsonian and Library of Congress researchers formed recently to examine some of the earliest American photographic collections and reference plates. We have used a range of microscopies, including digital light microscopy, portable imaging X-ray fluorescence spectrometry (imaging pXRF), scanning electron microscopy and X-ray microanalysis (SEM-EDS), and SEM-based micro-XRF to better understand these early technological changes.

Katrina Velle
UMass Dartmouth

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Bio​

Katrina Velle is a biologist interested in disease-causing microbes and evolutionary cell biology. She is investigating how the “brain-eating amoeba" crawls, eats, and divides.  She received her PhD in Molecular and Cell Biology from UConn in 2018, and worked with Dr. Fritz-Laylin at UMass Amherst for her postdoctoral research. She is now an Assistant Professor of Integrative Biology at UMass Dartmouth. Her work is supported by an NIH R00 Award (NIGMS), and Amazing Aven's Quest for Amoeba Awareness.

Abstract
The “brain-eating amoeba” crawls quickly and persistently in confined space

The “brain eating amoeba” Naegleria fowleri has a ~95% case fatality rate and primarily infects children. Despite its clear importance, we have little understanding of the basic cell biology that underlies Naegleria’s ability to cause disease, which is key information for the identification of new drug targets. To initiate an infection, Naegleria amoebae must crawl through narrow channels in the skull and through brain tissue, but how these cells crawl in these types of confined environments has been almost entirely unexplored. To study this process, we expose Naegleria to different types of confinement including microchannels. Using quantitative microscopy, we show that Naegleria amoebae seem to seek out confinement; after contacting the entrance to a microchannel, cells continue to probe the surface until they get inside. Once cells fully enter these channels, they crawl extremely quickly (up to 100 microns/min) in one direction for millimeters. While migrating in confined environments, cells show hallmarks of blebbing motility, in which the plasma membrane repeatedly blisters outward. Collectively, these data suggest that once Naegleria amoebae detect an opening to a narrow channel—similar to what they encounter during infection—cells will switch to blebbing motility to crawl quickly and persistently.

Audrey Medeiros
Massachusetts Life Science Center

Bio​

After receiving her Bachelor of Science degree from the University of Connecticut, Audrey worked for 3 years as a Research Assistant I/II at the Marine Biological Lab in Dr. Jennifer Morgan's lab using transmission electron microscopy to interrogate synaptic architecture of lamprey giant synapses. Audrey then earned her PhD from the Neuroscience Graduate Program at Brown University in Dr. Kate O'Connor-Giles lab. Her PhD dissertation investigated how calcium channel organization influences diverse synaptic properties using quantitative confocal imaging and the single molecule localization microscopy method STORM. After a short postdoc at Brown, Audrey joined the Massachusetts Life Science Center as a program manager where she helps fund innovative life science research throughout Massachusetts. In this role, Audrey manages 4 programs whose awards fund in demand imaging equipment and transformative infrastructure at non-profit research institutions.

Amy Reynolds
Boston Police Department

Bio​

Amy Reynolds is currently employed as a Criminalist IV, in charge of the Trace Evidence Section at the Boston Police Department Crime Laboratory.  Mrs. Reynolds has worked at this lab for over 24 years in various positions.  She holds a Bachelor of Arts in Biochemistry from the University of Colorado and a Master of Science in Forensic Science from the University of Illinois, Chicago.  She has a background in both trace evidence and criminalistics, and provides expert testimony in such areas as trace evidence, general criminalistics, crime scene processing, and bloodstain pattern analysis. She is certified in Hairs and Fibers, and Criminalistics with the American Board of Criminalistics (ABC) and is a Certified Crime Scene Investigator through the International Association for Identification (IAI).  She currently holds an exam coordinator position on the ABC Exam committee, overseeing the Foundational Knowledge Examination.  Mrs. Reynolds has been an adjunct instructor at several colleges and universities in Boston, with her most recent tenure as an adjunct professor, teaching the Trace Evidence lecture and laboratory courses in the Boston University Biomedical Forensic Science Master’s program. 

Tim Ross-Elliott
Oxford Instruments Andor

Bio​

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Simon Norrelyke

Harvard Medical School

Bio​

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Corporate Sponsors

Thank you for supporting NESM!

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AMETEK
Andor

Bruker
Carl Zeiss
Direct Electron, LP
EDAXX/Gatan

Evident Scientific
JEOL USA, Inc.

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Leica

Nikon Instruments, Inc.
Oxford Instruments
Prior Scientific

Rave Scientific
Tescan USA
Thermo Fisher Scientific

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