Uploaded July 2024 | Updated September 2026, 2 weeks ago
Joshua Goldberg is visiting OIST from 2024-06-26 until 2024-09-03 through the "Theoretical Sciences Visiting Program" (TSVP). Find out more about the TSVP on the program website:
oist.jp/visiting-program.
Title: What They Didn’t Tell Us in Computational Neuroscience 101: Studying Nonlinear Dendritic Integration and Network Entrainment in Pacemaking Neurons
Abstract: To simplify the description of neurons, neuroscience students are taught that neurons have a resting membrane potential (RMP), and require excitatory synaptic input to drive them to action potential threshold. Then, to simplify how neurons function in networks, neurons are treated as iso-potential (point-like) entities connected by synaptic weights. The first simplification is a prejudiced view that disregards diverse and ubiquitous classes of autonomously pacemaking neurons (that do not possess a stable RMP) in the brain. The second simplification disregards the complexity that dendrites add to the functions and calculations carried out by neurons. In my talk, I will describe my research that is aimed at making the contribution of dendrites to the response properties of pacemakers amenable to experimental investigation with currently available electrophysiological and optogenetic techniques. I will begin by introducing how the phase reduction formalism, provides a general framework for studying pacemakers, and present a recent study on how the framework explains spike correlations that appear in parkinsonism. I will then present how we used this formalism to study the role of dendrites in pacemaking neurons in the basal ganglia. We show that dendrites have a direct impact on how neurons encode their inputs and are entrained by them, and that we can use our formalism to probe the dendritic distribution of membrane non-linearities.
Profile: Dr. Joshua A. Goldberg is an associate professor of medical neurobiology at the Hebrew University of Jerusalem, Israel. His research focuses on the pathophysiology of movement disorders, most prominently Parkinson’s disease (PD). He combines advanced electrophysiology and imaging techniques both in vivo and in vitro with computational approaches to study how the physiology of neurons leads to their vulnerability in early statges of PD and how brain networks dynamics adapt to PD. He is a past recepient of a European Research Council (ERC) Consolidator grant and a Human Frontier Science Program (HFSP) grant with Dr. Jeff Wickens, OIST.
#OIST #OIST_TSVP #Neuroscience #Pacemaking #Neurons #Dendrites #Theoretical #Science #VisitingProgram #Okinawa #TSVP
Joshua Goldberg is visiting OIST from 2024-06-26 until 2024-09-03 through the "Theoretical Sciences Visiting Program" (TSVP). Find out more about the TSVP on the program website:
oist.jp/visiting-program.
Title: What They Didn’t Tell Us in Computational Neuroscience 101: Studying Nonlinear Dendritic Integration and Network Entrainment in Pacemaking Neurons
Abstract: To simplify the description of neurons, neuroscience students are taught that neurons have a resting membrane potential (RMP), and require excitatory synaptic input to drive them to action potential threshold. Then, to simplify how neurons function in networks, neurons are treated as iso-potential (point-like) entities connected by synaptic weights. The first simplification is a prejudiced view that disregards diverse and ubiquitous classes of autonomously pacemaking neurons (that do not possess a stable RMP) in the brain. The second simplification disregards the complexity that dendrites add to the functions and calculations carried out by neurons. In my talk, I will describe my research that is aimed at making the contribution of dendrites to the response properties of pacemakers amenable to experimental investigation with currently available electrophysiological and optogenetic techniques. I will begin by introducing how the phase reduction formalism, provides a general framework for studying pacemakers, and present a recent study on how the framework explains spike correlations that appear in parkinsonism. I will then present how we used this formalism to study the role of dendrites in pacemaking neurons in the basal ganglia. We show that dendrites have a direct impact on how neurons encode their inputs and are entrained by them, and that we can use our formalism to probe the dendritic distribution of membrane non-linearities.
Profile: Dr. Joshua A. Goldberg is an associate professor of medical neurobiology at the Hebrew University of Jerusalem, Israel. His research focuses on the pathophysiology of movement disorders, most prominently Parkinson’s disease (PD). He combines advanced electrophysiology and imaging techniques both in vivo and in vitro with computational approaches to study how the physiology of neurons leads to their vulnerability in early statges of PD and how brain networks dynamics adapt to PD. He is a past recepient of a European Research Council (ERC) Consolidator grant and a Human Frontier Science Program (HFSP) grant with Dr. Jeff Wickens, OIST.
#OIST #OIST_TSVP #Neuroscience #Pacemaking #Neurons #Dendrites #Theoretical #Science #VisitingProgram #Okinawa #TSVP




![Provost Lecture Series: Yejun Feng
Speaker: Yejun Feng, Professor, Electronic and Quantum Magnetism Unit
Title: Where physics is not enough...
Abstract:
Over the past several decades, there has existed abundant amount of physics interest in materials with a pyrochlore sublattice, which can potentially host spin frustrations in the three-dimensional space and lead to exotic spin states of either trivial or non-trivial topological properties. However, experimentally, even the ground state of spinel ZnFe2O4, a classical spin system that had been studied over seventy years, had not been clearly resolved. With arduous efforts from my former Ph.D. student Margarita Dronova and many former and current Unit members, we experimentally improved the chemical quality by limiting various types of disorder in single crystal ZnFe2O4 to a total level of ~0.2% [1]. Such high-quality crystals allow a clarification of the long-range antiferromagnetic ground state with a three-dimensional checkerboard pattern [2]. This full control of materials’ chemistry enables us to further explore the experimental identity of spin glass. Here we introduce non-magnetic cations into ZnFe2O4 in a controlled manner by limiting them only to pyrochlore but no other sites. This destruction of a long-range order draws a similarity to the paradigm of quantum criticality, and the minimal amount of disorder used to drive this evolution allows one to explore spin glass in its emergent state, in the proximity of either long- or short-range order. Neutron magnetic diffuse scattering, probing at pico-second time scale, provides key separations between the entities of long-, short-range orders and spin glass [3].
Reference:
[1] Dronova et al., PNAS 119, e2208748119 (2022).
[2] Dronova et al., PRB 109, 064421 (2024), with Editor’s Suggestion.
[3] Dronova et al., Arxiv:2507.07783.
Chair: Pinaki Chakraborty, Professor, Fluid Mechanics Unit Provost Lecture Series: Yejun Feng](https://i.ytimg.com/vi/BoygP934LeE/mqdefault.jpg)

![[Seminar] Making eDNA data FAIR (Findable, Accessible, Interoperable, Reusable)
Seminar title: Making eDNA data FAIR (Findable, Accessible, Interoperable, Reusable)
Speaker: Dr. Miwa Takahashi, CERC Postdoctoral Fellow, Environomics Future Science Platform, NCMI | CSIRO
Friday, August 30, 2024 - 13:00 to 14:00
Environmental DNA (eDNA) has emerged as a powerful monitoring tool for species detection and distribution mapping, with a remarkable surge in activity over the past decade. Metabarcoding studies have generated millions of DNA sequences with taxonomic assignments, while species-specific eDNA assays have produced comprehensive distribution maps for hundreds of taxa. Despite the widespread practice of data sharing upon publication, inconsistent data formats pose challenges for data reuse. To address this issue, the “Making eDNA FAIR (Findable, Accessible, Interoperable, Reusable)” project has been launched. Our international, multidisciplinary working group, consisting of eDNA researchers, journal editors and biodiversity and omics data scientists, is developing best practice guidelines for eDNA data formatting and sharing. Our aim is to extend the eDNA data lifecycle, facilitating reuse and reanalyses of this invaluable biodiversity data resource. Please join our seminar to learn about the FAIR data principles and the project, and start our discussions on the bottlenecks, needs, and strategies to achieve FAIR eDNA!
https://groups.oist.jp/macc/event/seminar-making-edna-data-fair-findable-accessible-interoperable-reusable [Seminar] Making eDNA data FAIR (Findable, Accessible, Interoperable, Reusable)](https://i.ytimg.com/vi/Cxb1RMoVpwE/mqdefault.jpg)



