top of page
2025 NESM Flyer - EM color - Link.png

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.

​

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

​

9 am

9:15 am

10 am 

10:15 am

10:30 am 

10:45 am

12 pm

12:15 pm

1 pm 



 

1:50 pm

2:05 pm

2:15 pm 

2:30 pm

 

3:00 pm

3:50 pm

​

​

​

Welcome from the NESM Board

Keynote - Edward Vicenzi

Hangjian Ling (UMass Dartmouth)

[Coffee Break]

Ashley Cavanagh (Harvard)

Microscopy Career Panel

Heather Brown-Harding (HCBI)

[Lunch]

Vendor Flash Talks
- JEOL

- SyGlass

- Rave Scientific
- Nanoscience Instruments
Dina Hashoul
(MGH)

[Coffee Break]

Mark Scimone (UNH Manchester)

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

Keynote - Katrina Velle

Closing Remarks

​

Keynote Speakers

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

Ed-Vi_edited.png

Museum Conservation Institute

Smithsonian Institution

Katrina Velle Headshot_edited.jpg

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)

AudreyMedeiros_3.jpg

Massachusetts Life Science Center

DSC_0422.JPG

Boston Police Department

Tim_Ross_Elliott.jpg

Oxford Instruments Andor

Simon Norrelyke.PNG

Harvard Medical School

Lytton-Jean-Abigail_0384-Preferred.jpg

Koch Institute

Speakers selected from Abstracts

Hangjian Lin (UMass Dartmouth) - Study of bacterial surface interactions by scanning electron microscopy and digital holographic micrscopy
Ashley Cavanagh (Harvard) - Scanning Transmission Electron Microscope Characterization of the Atomic and Ferroelectric Microstructure of Thin-Film BaTiO3
Heather Brown-Harding (HCBI) - Leasing Microscopes for a Core Facility
Dina Hashoul (MGH) - using 2-photon microscopy to study Alzheimer's disease progression
Mark Scimone (UNH Manchester) - traction force microscopy using STED super-resolution

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

Katrina Velle Headshot.png
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

Tim_Ross_Elliott_edited.jpg
Bio​

Tim initially ventured into the world of microscopy as an undergraduate at Washington State University working in a plant biology lab for a PI who was faculty director of the light and electron microscopy facility. Subsequent graduate research in molecular biology deepened his interest in microscopy as a primary tool for scientific discovery. Following the academic career trajectory, a postdoc at UNC Chapel Hill and position as an Advanced Imaging Specialist at the MicRoN core at Harvard Medical School broadened Tim's experience with numerous additional imaging modalities. In 2021 Tim was recruited to Andor Technology as an Applications Specialist to support customers during demos and with post-installation training and workflow support. Since April 2022 he have been responsible for sales spinning disk confocals and loves consulting with new groups to support their exciting microscopy-based research projects.

Simon Nørrelyke
Harvard Medical School

Simon Norrelyke.PNG
Bio​

Simon is director of the Image Analysis Collaboratory (IAC) and lecturer on Systems Biology at the Blavatnik Institute at Harvard Medical School. His research interests include classic image analysis, deep learning, spatial statistics, and causal inference. At the IAC he works closely with the local life-scientists—teaching, training, and collaborating on image and data analysis projects of all sizes.
Simon holds a Ph.D. in Physics from the Niels Bohr Institute at Copenhagen University (Denmark) and has since worked in Florence (Italy), Dresden (Germany), Princeton (NJ, USA), and Zurich (Switzerland). His past research spans econo-physics, optical tweezers, single-molecule biophysics, and cell migration.

Abigail Lytton-Jean
Koch Institute

Lytton-Jean-Abigail_0384-Preferred.jpg
Bio​

Abigail Lytton-Jean is the founder and scientific director of the Peterson (1957) Nanotechnology Materials Core Facility at the Koch Institute. Her core facility addresses nano and materials characterization of bio-relevant materials with a strong emphasis on multiscale cryo-electron microscopy (cryoEM). Of particular significance are bespoke, cutting-edge sample preparation and cryo workflows that enable EM and correlation between light and electron microscopy (CLEM). These sample preparation and imaging workflows allow for the orchestration of multiscale structural imaging of cells, tissue, and synthetic materials while providing pinpoint accuracy of desired regions of interest with nanometer scale resolution. 

Lytton-Jean is a chemist by training with concentrated expertise in biological and inorganic nanomaterials. She conducted her graduate studies with Professor Chad Mirkin at Northwestern University, working with DNA-modified gold nanoparticles, characterizing fundamental properties, designing detection platforms, and generating programmable materials to control and direct nano assembly. Her postdoctoral work was completed under the direction of Professors Robert Langer and Daniel Anderson at MIT, and focused on biodegradable nanoparticle synthesis for intracellular RNA delivery.

Corporate Sponsors

Thank you for supporting NESM!

​

AMETEK
Andor

Bruker
Carl Zeiss
Direct Electron, LP
EDAXX/Gatan

Evident Scientific
JEOL USA, Inc.

​

​

Leica

Nikon Instruments, Inc.
Oxford Instruments
Prior Scientific

Rave Scientific
Tescan USA
Thermo Fisher Scientific

© 2035 by Site Name. Powered and secured by Wix

bottom of page