---
OA_place: publisher
_id: '11128'
abstract:
- lang: eng
  text: "Although we often see studies focusing on simple or even discrete traits
    in studies of colouration,\r\nthe variation of “appearance” phenotypes found in
    nature is often more complex, continuous\r\nand high-dimensional. Therefore, we
    developed automated methods suitable for large datasets\r\nof genomes and images,
    striving to account for their complex nature, while minimising human\r\nbias.
    We used these methods on a dataset of more than 20, 000 plant SNP genomes and\r\ncorresponding
    fower images from a hybrid zone of two subspecies of Antirrhinum majus with\r\ndistinctly
    coloured fowers to improve our understanding of the genetic nature of the fower\r\ncolour
    in our study system.\r\nFirstly, we use the advantage of large numbers of genotyped
    plants to estimate the haplotypes in\r\nthe main fower colour regulating region.
    We study colour- and geography-related characteristics\r\nof the estimated haplotypes
    and how they connect to their relatedness. We show discrepancies\r\nfrom the expected
    fower colour distributions given the genotype and identify particular\r\nhaplotypes
    leading to unexpected phenotypes. We also confrm a signifcant defcit of the\r\ndouble
    recessive recombinant and quite surprisingly, we show that haplotypes of the most\r\nfrequent
    parental type are much less variable than others.\r\nSecondly, we introduce our
    pipeline capable of processing tens of thousands of full fower\r\nimages without
    human interaction and summarising each image into a set of informative scores.\r\nWe
    show the compatibility of these machine-measured fower colour scores with the
    previously\r\nused manual scores and study impact of external efect on the resulting
    scores. Finally, we use\r\nthe machine-measured fower colour scores to ft and
    examine a phenotype cline across the\r\nhybrid zone in Planoles using full fower
    images as opposed to discrete, manual scores and\r\ncompare it with the genotypic
    cline."
acknowledged_ssus:
- _id: ScienComp
- _id: Bio
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Lenka
  full_name: Matejovicova, Lenka
  id: 2DFDEC72-F248-11E8-B48F-1D18A9856A87
  last_name: Matejovicova
citation:
  ama: Matejovicova L. Genetic basis of flower colour as a model for adaptive evolution.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:11128">10.15479/at:ista:11128</a>
  apa: Matejovicova, L. (2022). <i>Genetic basis of flower colour as a model for adaptive
    evolution</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11128">https://doi.org/10.15479/at:ista:11128</a>
  chicago: Matejovicova, Lenka. “Genetic Basis of Flower Colour as a Model for Adaptive
    Evolution.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11128">https://doi.org/10.15479/at:ista:11128</a>.
  ieee: L. Matejovicova, “Genetic basis of flower colour as a model for adaptive evolution,”
    Institute of Science and Technology Austria, 2022.
  ista: Matejovicova L. 2022. Genetic basis of flower colour as a model for adaptive
    evolution. Institute of Science and Technology Austria.
  mla: Matejovicova, Lenka. <i>Genetic Basis of Flower Colour as a Model for Adaptive
    Evolution</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11128">10.15479/at:ista:11128</a>.
  short: L. Matejovicova, Genetic Basis of Flower Colour as a Model for Adaptive Evolution,
    Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-04-07T08:19:54Z
date_published: 2022-04-06T00:00:00Z
date_updated: 2026-04-07T14:12:19Z
day: '06'
ddc:
- '576'
- '582'
degree_awarded: PhD
department:
- _id: GradSch
- _id: NiBa
doi: 10.15479/at:ista:11128
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language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: '112'
publication_identifier:
  isbn:
  - 978-3-99078-016-9
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
title: Genetic basis of flower colour as a model for adaptive evolution
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
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...
---
OA_place: publisher
_id: '12072'
abstract:
- lang: eng
  text: "In this thesis, we study two of the most important questions in Arithmetic
    geometry: that of the existence and density of solutions to Diophantine equations.
    In order for a Diophantine equation to have any solutions over the rational numbers,
    it must have solutions everywhere locally, i.e., over R and over Qp for every
    prime p. The converse, called the Hasse principle, is known to fail in general.
    However, it is still a central question in Arithmetic geometry to determine for
    which varieties the Hasse principle does hold. In this work, we establish the
    Hasse principle for a wide new family of varieties of the form f(t) = NK/Q(x)
    ̸= 0, where f is a polynomial with integer coefficients and NK/Q denotes the norm\r\nform
    associated to a number field K. Our results cover products of arbitrarily many
    linear, quadratic or cubic factors, and generalise an argument of Irving [69],
    which makes use of the beta sieve of Rosser and Iwaniec. We also demonstrate how
    our main sieve results can be applied to treat new cases of a conjecture of Harpaz
    and Wittenberg on locally split values of polynomials over number fields, and
    discuss consequences for rational points in fibrations.\r\nIn the second question,
    about the density of solutions, one defines a height function and seeks to estimate
    asymptotically the number of points of height bounded by B as B → ∞. Traditionally,
    one either counts rational points, or\r\nintegral points with respect to a suitable
    model. However, in this thesis, we study an emerging area of interest in Arithmetic
    geometry known as Campana points, which in some sense interpolate between rational
    and integral points.\r\nMore precisely, we count the number of nonzero integers
    z1, z2, z3 such that gcd(z1, z2, z3) = 1, and z1, z2, z3, z1 + z2 + z3 are all
    squareful and bounded by B. Using the circle method, we obtain an asymptotic formula
    which agrees in\r\nthe power of B and log B with a bold new generalisation of
    Manin’s conjecture to the setting of Campana points, recently formulated by Pieropan,
    Smeets, Tanimoto and Várilly-Alvarado [96]. However, in this thesis we also provide
    the first known counterexamples to leading constant predicted by their conjecture. "
acknowledgement: I acknowledge the received funding from the European Union’s Horizon
  2020 research and innovation programme under the Marie Sklodowska Curie Grant Agreement
  No. 665385.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Alec L
  full_name: Shute, Alec L
  id: 440EB050-F248-11E8-B48F-1D18A9856A87
  last_name: Shute
  orcid: 0000-0002-1812-2810
citation:
  ama: 'Shute AL. Existence and density problems in Diophantine geometry: From norm
    forms to Campana points. 2022. doi:<a href="https://doi.org/10.15479/at:ista:12072">10.15479/at:ista:12072</a>'
  apa: 'Shute, A. L. (2022). <i>Existence and density problems in Diophantine geometry:
    From norm forms to Campana points</i>. Institute of Science and Technology Austria.
    <a href="https://doi.org/10.15479/at:ista:12072">https://doi.org/10.15479/at:ista:12072</a>'
  chicago: 'Shute, Alec L. “Existence and Density Problems in Diophantine Geometry:
    From Norm Forms to Campana Points.” Institute of Science and Technology Austria,
    2022. <a href="https://doi.org/10.15479/at:ista:12072">https://doi.org/10.15479/at:ista:12072</a>.'
  ieee: 'A. L. Shute, “Existence and density problems in Diophantine geometry: From
    norm forms to Campana points,” Institute of Science and Technology Austria, 2022.'
  ista: 'Shute AL. 2022. Existence and density problems in Diophantine geometry: From
    norm forms to Campana points. Institute of Science and Technology Austria.'
  mla: 'Shute, Alec L. <i>Existence and Density Problems in Diophantine Geometry:
    From Norm Forms to Campana Points</i>. Institute of Science and Technology Austria,
    2022, doi:<a href="https://doi.org/10.15479/at:ista:12072">10.15479/at:ista:12072</a>.'
  short: 'A.L. Shute, Existence and Density Problems in Diophantine Geometry: From
    Norm Forms to Campana Points, Institute of Science and Technology Austria, 2022.'
corr_author: '1'
date_created: 2022-09-08T21:53:03Z
date_published: 2022-09-08T00:00:00Z
date_updated: 2026-04-07T14:13:35Z
day: '08'
ddc:
- '512'
degree_awarded: PhD
department:
- _id: GradSch
- _id: TiBr
doi: 10.15479/at:ista:12072
ec_funded: 1
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  date_created: 2022-09-08T21:50:34Z
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language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '208'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  isbn:
  - 978-3-99078-023-7
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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  - id: '12076'
    relation: part_of_dissertation
    status: public
  - id: '12077'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Timothy D
  full_name: Browning, Timothy D
  id: 35827D50-F248-11E8-B48F-1D18A9856A87
  last_name: Browning
  orcid: 0000-0002-8314-0177
title: 'Existence and density problems in Diophantine geometry: From norm forms to
  Campana points'
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  image: /images/cc_by_nc_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
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  short: CC BY-NC-SA (4.0)
type: dissertation
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...
---
OA_place: publisher
_id: '11777'
abstract:
- lang: eng
  text: "In this dissertation we study coboundary expansion of simplicial complex
    with a view of giving geometric applications.\r\nOur main novel tool is an equivariant
    version of Gromov's celebrated Topological Overlap Theorem. The equivariant topological
    overlap theorem leads to various geometric applications including a quantitative
    non-embeddability result for sufficiently thick buildings (which partially resolves
    a conjecture of Tancer and Vorwerk) and an improved lower bound on the pair-crossing
    number of (bounded degree) expander graphs. Additionally, we will give new proofs
    for several known lower bounds for geometric problems such as the number of Tverberg
    partitions or the crossing number of complete bipartite graphs.\r\nFor the aforementioned
    applications one is naturally lead to study expansion properties of joins of simplicial
    complexes. In the presence of a special certificate for expansion (as it is the
    case, e.g., for spherical buildings), the join of two expanders is an expander.
    On the flip-side, we report quite some evidence that coboundary expansion exhibits
    very non-product-like behaviour under taking joins. For instance, we exhibit infinite
    families of graphs $(G_n)_{n\\in \\mathbb{N}}$ and $(H_n)_{n\\in\\mathbb{N}}$
    whose join $G_n*H_n$ has expansion of lower order than the product of the expansion
    constant of the graphs. Moreover, we show an upper bound of $(d+1)/2^d$ on the
    normalized coboundary expansion constants for the complete multipartite complex
    $[n]^{*(d+1)}$ (under a mild divisibility condition on $n$).\r\nVia the probabilistic
    method the latter result extends to an upper bound of $(d+1)/2^d+\\varepsilon$
    on the coboundary expansion constant of the spherical building associated with
    $\\mathrm{PGL}_{d+2}(\\mathbb{F}_q)$ for any $\\varepsilon>0$ and sufficiently
    large $q=q(\\varepsilon)$. This disproves a conjecture of Lubotzky, Meshulam and
    Mozes -- in a rather strong sense.\r\nBy improving on existing lower bounds we
    make further progress towards closing the gap between the known lower and upper
    bounds on the coboundary expansion constants of $[n]^{*(d+1)}$. The best improvements
    we achieve using computer-aided proofs and flag algebras. The exact value even
    for the complete $3$-partite $2$-dimensional complex $[n]^{*3}$ remains unknown
    but we are happy to conjecture a precise value for every $n$. %Moreover, we show
    that a previously shown lower bound on the expansion constant of the spherical
    building associated with $\\mathrm{PGL}_{2}(\\mathbb{F}_q)$ is not tight.\r\nIn
    a loosely structured, last chapter of this thesis we collect further smaller observations
    related to expansion. We point out a link between discrete Morse theory and a
    technique for showing coboundary expansion, elaborate a bit on the hardness of
    computing coboundary expansion constants, propose a new criterion for coboundary
    expansion (in a very dense setting) and give one way of making the folklore result
    that expansion of links is a necessary condition for a simplicial complex to be
    an expander precise."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Pascal
  full_name: Wild, Pascal
  id: 4C20D868-F248-11E8-B48F-1D18A9856A87
  last_name: Wild
citation:
  ama: Wild P. High-dimensional expansion and crossing numbers of simplicial complexes.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:11777">10.15479/at:ista:11777</a>
  apa: Wild, P. (2022). <i>High-dimensional expansion and crossing numbers of simplicial
    complexes</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11777">https://doi.org/10.15479/at:ista:11777</a>
  chicago: Wild, Pascal. “High-Dimensional Expansion and Crossing Numbers of Simplicial
    Complexes.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11777">https://doi.org/10.15479/at:ista:11777</a>.
  ieee: P. Wild, “High-dimensional expansion and crossing numbers of simplicial complexes,”
    Institute of Science and Technology Austria, 2022.
  ista: Wild P. 2022. High-dimensional expansion and crossing numbers of simplicial
    complexes. Institute of Science and Technology Austria.
  mla: Wild, Pascal. <i>High-Dimensional Expansion and Crossing Numbers of Simplicial
    Complexes</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11777">10.15479/at:ista:11777</a>.
  short: P. Wild, High-Dimensional Expansion and Crossing Numbers of Simplicial Complexes,
    Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-08-10T15:51:19Z
date_published: 2022-08-11T00:00:00Z
date_updated: 2026-04-07T14:18:26Z
day: '11'
ddc:
- '500'
- '516'
- '514'
degree_awarded: PhD
department:
- _id: GradSch
- _id: UlWa
doi: 10.15479/at:ista:11777
ec_funded: 1
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  date_updated: 2022-08-10T15:34:04Z
  description: Code for computer-assisted proofs in Section 8.4.7 in Thesis
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  date_created: 2022-08-10T15:34:10Z
  date_updated: 2022-08-10T15:34:10Z
  description: Code for proof of Lemma 8.20 in Thesis
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  date_created: 2022-08-10T15:34:17Z
  date_updated: 2022-08-10T15:34:17Z
  description: Code for proof of Proposition 7.9 in Thesis
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  date_created: 2022-08-11T16:08:33Z
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  date_created: 2022-08-11T16:09:19Z
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  file_name: ThesisSubmission.zip
  file_size: 18150068
  relation: source_file
file_date_updated: 2022-08-11T16:09:19Z
has_accepted_license: '1'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: '170'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  isbn:
  - 978-3-99078-021-3
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Uli
  full_name: Wagner, Uli
  id: 36690CA2-F248-11E8-B48F-1D18A9856A87
  last_name: Wagner
  orcid: 0000-0002-1494-0568
title: High-dimensional expansion and crossing numbers of simplicial complexes
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '10799'
abstract:
- lang: eng
  text: "Because of the increasing popularity of machine learning methods, it is becoming
    important to understand the impact of learned components on automated decision-making
    systems and to guarantee that their consequences are beneficial to society. In
    other words, it is necessary to ensure that machine learning is sufficiently trustworthy
    to be used in real-world applications. This thesis studies two properties of machine
    learning models that are highly desirable for the\r\nsake of reliability: robustness
    and fairness. In the first part of the thesis we study the robustness of learning
    algorithms to training data corruption. Previous work has shown that machine learning
    models are vulnerable to a range\r\nof training set issues, varying from label
    noise through systematic biases to worst-case data manipulations. This is an especially
    relevant problem from a present perspective, since modern machine learning methods
    are particularly data hungry and therefore practitioners often have to rely on
    data collected from various external sources, e.g. from the Internet, from app
    users or via crowdsourcing. Naturally, such sources vary greatly in the quality
    and reliability of the\r\ndata they provide. With these considerations in mind,
    we study the problem of designing machine learning algorithms that are robust
    to corruptions in data coming from multiple sources. We show that, in contrast
    to the case of a single dataset with outliers, successful learning within this
    model is possible both theoretically and practically, even under worst-case data
    corruptions. The second part of this thesis deals with fairness-aware machine
    learning. There are multiple areas where machine learning models have shown promising
    results, but where careful considerations are required, in order to avoid discrimanative
    decisions taken by such learned components. Ensuring fairness can be particularly
    challenging, because real-world training datasets are expected to contain various
    forms of historical bias that may affect the learning process. In this thesis
    we show that data corruption can indeed render the problem of achieving fairness
    impossible, by tightly characterizing the theoretical limits of fair learning
    under worst-case data manipulations. However, assuming access to clean data, we
    also show how fairness-aware learning can be made practical in contexts beyond
    binary classification, in particular in the challenging learning to rank setting."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Nikola H
  full_name: Konstantinov, Nikola H
  id: 4B9D76E4-F248-11E8-B48F-1D18A9856A87
  last_name: Konstantinov
  orcid: 0009-0009-5204-7621
citation:
  ama: Konstantinov NH. Robustness and fairness in machine learning. 2022. doi:<a
    href="https://doi.org/10.15479/at:ista:10799">10.15479/at:ista:10799</a>
  apa: Konstantinov, N. H. (2022). <i>Robustness and fairness in machine learning</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:10799">https://doi.org/10.15479/at:ista:10799</a>
  chicago: Konstantinov, Nikola H. “Robustness and Fairness in Machine Learning.”
    Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:10799">https://doi.org/10.15479/at:ista:10799</a>.
  ieee: N. H. Konstantinov, “Robustness and fairness in machine learning,” Institute
    of Science and Technology Austria, 2022.
  ista: Konstantinov NH. 2022. Robustness and fairness in machine learning. Institute
    of Science and Technology Austria.
  mla: Konstantinov, Nikola H. <i>Robustness and Fairness in Machine Learning</i>.
    Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:10799">10.15479/at:ista:10799</a>.
  short: N.H. Konstantinov, Robustness and Fairness in Machine Learning, Institute
    of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-02-28T13:03:49Z
date_published: 2022-03-08T00:00:00Z
date_updated: 2026-04-07T14:19:48Z
day: '08'
ddc:
- '000'
degree_awarded: PhD
department:
- _id: GradSch
- _id: ChLa
doi: 10.15479/at:ista:10799
ec_funded: 1
file:
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  checksum: 626bc523ae8822d20e635d0e2d95182e
  content_type: application/pdf
  creator: nkonstan
  date_created: 2022-03-06T11:42:54Z
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has_accepted_license: '1'
keyword:
- robustness
- fairness
- machine learning
- PAC learning
- adversarial learning
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: '176'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  isbn:
  - 978-3-99078-015-2
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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    relation: part_of_dissertation
    status: public
  - id: '8724'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
title: Robustness and fairness in machine learning
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
_id: '11344'
abstract:
- lang: eng
  text: Until recently, Shigella and enteroinvasive Escherichia coli were thought
    to be primate-restricted pathogens. The base of their pathogenicity is the type
    3 secretion system (T3SS) encoded by the pINV virulence plasmid, which facilitates
    host cell invasion and subsequent proliferation. A large family of T3SS effectors,
    E3 ubiquitin-ligases encoded by the ipaH genes, have a key role in the Shigella
    pathogenicity through the modulation of cellular ubiquitination that degrades
    host proteins. However, recent genomic studies identified ipaH genes in the genomes
    of Escherichia marmotae, a potential marmot pathogen, and an E. coli extracted
    from fecal samples of bovine calves, suggesting that non-human hosts may also
    be infected by these strains, potentially pathogenic to humans. We performed a
    comparative genomic study of the functional repertoires in the ipaH gene family
    in Shigella and enteroinvasive Escherichia from human and predicted non-human
    hosts. We found that fewer than half of Shigella genomes had a complete set of
    ipaH genes, with frequent gene losses and duplications that were not consistent
    with the species tree and nomenclature. Non-human host IpaH proteins had a diverse
    set of substrate-binding domains and, in contrast to the Shigella proteins, two
    variants of the NEL C-terminal domain. Inconsistencies between strains phylogeny
    and composition of effectors indicate horizontal gene transfer between E. coli
    adapted to different hosts. These results provide a framework for understanding
    of ipaH-mediated host-pathogens interactions and suggest a need for a genomic
    study of fecal samples from diseased animals.
acknowledgement: 'The project was initiated with Aygul Minnegalieva and Yulia Yakovleva
  at the Summer School of Molecular and Theoretical Biology (SMTB-2020), supported
  by the Zimin Foundation. We thank Inna Shapovalenko, Daria Abuzova, Elizaveta Kaminskaya,
  and Dmitriy Zvezdin for their contribution to the project during SMTB-2020. We also
  thank Peter Vlasov for fruitful discussions.This study was supported by the Russian
  Foundation for Basic Research (RFBR), Grant # 20-54-14005 and Fonds zur Förderung
  der wissenschaftlichen Forschung (FWF), Grant # I5127-B. The work of OB is supported
  by the European Union’s Horizon 2020 Research and Innovation Programme under the
  Marie Skłodowska-Curie Grant Agreement No. 754411. '
article_number: '6868'
article_processing_charge: No
article_type: original
author:
- first_name: NO
  full_name: Dranenko, NO
  last_name: Dranenko
- first_name: MN
  full_name: Tutukina, MN
  last_name: Tutukina
- first_name: MS
  full_name: Gelfand, MS
  last_name: Gelfand
- first_name: Fyodor
  full_name: Kondrashov, Fyodor
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
- first_name: Olga
  full_name: Bochkareva, Olga
  id: C4558D3C-6102-11E9-A62E-F418E6697425
  last_name: Bochkareva
  orcid: 0000-0003-1006-6639
citation:
  ama: Dranenko N, Tutukina M, Gelfand M, Kondrashov F, Bochkareva O. Chromosome-encoded
    IpaH ubiquitin ligases indicate non-human enteroinvasive Escherichia. <i>Scientific
    Reports</i>. 2022;12. doi:<a href="https://doi.org/10.1038/s41598-022-10827-3">10.1038/s41598-022-10827-3</a>
  apa: Dranenko, N., Tutukina, M., Gelfand, M., Kondrashov, F., &#38; Bochkareva,
    O. (2022). Chromosome-encoded IpaH ubiquitin ligases indicate non-human enteroinvasive
    Escherichia. <i>Scientific Reports</i>. Springer Nature. <a href="https://doi.org/10.1038/s41598-022-10827-3">https://doi.org/10.1038/s41598-022-10827-3</a>
  chicago: Dranenko, NO, MN Tutukina, MS Gelfand, Fyodor Kondrashov, and Olga Bochkareva.
    “Chromosome-Encoded IpaH Ubiquitin Ligases Indicate Non-Human Enteroinvasive Escherichia.”
    <i>Scientific Reports</i>. Springer Nature, 2022. <a href="https://doi.org/10.1038/s41598-022-10827-3">https://doi.org/10.1038/s41598-022-10827-3</a>.
  ieee: N. Dranenko, M. Tutukina, M. Gelfand, F. Kondrashov, and O. Bochkareva, “Chromosome-encoded
    IpaH ubiquitin ligases indicate non-human enteroinvasive Escherichia,” <i>Scientific
    Reports</i>, vol. 12. Springer Nature, 2022.
  ista: Dranenko N, Tutukina M, Gelfand M, Kondrashov F, Bochkareva O. 2022. Chromosome-encoded
    IpaH ubiquitin ligases indicate non-human enteroinvasive Escherichia. Scientific
    Reports. 12, 6868.
  mla: Dranenko, NO, et al. “Chromosome-Encoded IpaH Ubiquitin Ligases Indicate Non-Human
    Enteroinvasive Escherichia.” <i>Scientific Reports</i>, vol. 12, 6868, Springer
    Nature, 2022, doi:<a href="https://doi.org/10.1038/s41598-022-10827-3">10.1038/s41598-022-10827-3</a>.
  short: N. Dranenko, M. Tutukina, M. Gelfand, F. Kondrashov, O. Bochkareva, Scientific
    Reports 12 (2022).
corr_author: '1'
date_created: 2022-05-02T07:08:42Z
date_published: 2022-04-27T00:00:00Z
date_updated: 2026-04-15T08:51:09Z
day: '27'
ddc:
- '570'
department:
- _id: FyKo
doi: 10.1038/s41598-022-10827-3
ec_funded: 1
external_id:
  isi:
  - '000788639400032'
  pmid:
  - '35477739'
file:
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has_accepted_license: '1'
intvolume: '        12'
isi: 1
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: 34e076d6-11ca-11ed-8bc3-aec76c41a181
  grant_number: I05127
  name: Evolutionary analysis of gene regulation
publication: Scientific Reports
publication_identifier:
  issn:
  - 2045-2322
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Chromosome-encoded IpaH ubiquitin ligases indicate non-human enteroinvasive
  Escherichia
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 12
year: '2022'
...
---
_id: '10774'
abstract:
- lang: eng
  text: We study the problem of specifying sequential information-flow properties
    of systems. Information-flow properties are hyperproperties, as they compare different
    traces of a system. Sequential information-flow properties can express changes,
    over time, in the information-flow constraints. For example, information-flow
    constraints during an initialization phase of a system may be different from information-flow
    constraints that are required during the operation phase. We formalize several
    variants of interpreting sequential information-flow constraints, which arise
    from different assumptions about what can be observed of the system. For this
    purpose, we introduce a first-order logic, called Hypertrace Logic, with both
    trace and time quantifiers for specifying linear-time hyperproperties. We prove
    that HyperLTL, which corresponds to a fragment of Hypertrace Logic with restricted
    quantifier prefixes, cannot specify the majority of the studied variants of sequential
    information flow, including all variants in which the transition between sequential
    phases (such as initialization and operation) happens asynchronously. Our results
    rely on new equivalences between sets of traces that cannot be distinguished by
    certain classes of formulas from Hypertrace Logic. This presents a new approach
    to proving inexpressiveness results for HyperLTL.
acknowledgement: This work was funded in part by the Wittgenstein Award Z211-N23 of
  the Austrian Science Fund (FWF) and by the FWF project W1255-N23.
alternative_title:
- LNCS
article_processing_charge: No
arxiv: 1
author:
- first_name: Ezio
  full_name: Bartocci, Ezio
  last_name: Bartocci
- first_name: Thomas
  full_name: Ferrere, Thomas
  id: 40960E6E-F248-11E8-B48F-1D18A9856A87
  last_name: Ferrere
  orcid: 0000-0001-5199-3143
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000-0002-2985-7724
- first_name: Dejan
  full_name: Nickovic, Dejan
  id: 41BCEE5C-F248-11E8-B48F-1D18A9856A87
  last_name: Nickovic
- first_name: Ana Oliveira
  full_name: Da Costa, Ana Oliveira
  last_name: Da Costa
citation:
  ama: 'Bartocci E, Ferrere T, Henzinger TA, Nickovic D, Da Costa AO. Flavors of sequential
    information flow. In: <i>Lecture Notes in Computer Science (Including Subseries
    Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)</i>.
    Vol 13182. Springer Nature; 2022:1-19. doi:<a href="https://doi.org/10.1007/978-3-030-94583-1_1">10.1007/978-3-030-94583-1_1</a>'
  apa: 'Bartocci, E., Ferrere, T., Henzinger, T. A., Nickovic, D., &#38; Da Costa,
    A. O. (2022). Flavors of sequential information flow. In <i>Lecture Notes in Computer
    Science (including subseries Lecture Notes in Artificial Intelligence and Lecture
    Notes in Bioinformatics)</i> (Vol. 13182, pp. 1–19). Philadelphia, PA, United
    States: Springer Nature. <a href="https://doi.org/10.1007/978-3-030-94583-1_1">https://doi.org/10.1007/978-3-030-94583-1_1</a>'
  chicago: Bartocci, Ezio, Thomas Ferrere, Thomas A Henzinger, Dejan Nickovic, and
    Ana Oliveira Da Costa. “Flavors of Sequential Information Flow.” In <i>Lecture
    Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence
    and Lecture Notes in Bioinformatics)</i>, 13182:1–19. Springer Nature, 2022. <a
    href="https://doi.org/10.1007/978-3-030-94583-1_1">https://doi.org/10.1007/978-3-030-94583-1_1</a>.
  ieee: E. Bartocci, T. Ferrere, T. A. Henzinger, D. Nickovic, and A. O. Da Costa,
    “Flavors of sequential information flow,” in <i>Lecture Notes in Computer Science
    (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes
    in Bioinformatics)</i>, Philadelphia, PA, United States, 2022, vol. 13182, pp.
    1–19.
  ista: 'Bartocci E, Ferrere T, Henzinger TA, Nickovic D, Da Costa AO. 2022. Flavors
    of sequential information flow. Lecture Notes in Computer Science (including subseries
    Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics).
    VMCAI: Verifcation, Model Checking, and Abstract Interpretation, LNCS, vol. 13182,
    1–19.'
  mla: Bartocci, Ezio, et al. “Flavors of Sequential Information Flow.” <i>Lecture
    Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence
    and Lecture Notes in Bioinformatics)</i>, vol. 13182, Springer Nature, 2022, pp.
    1–19, doi:<a href="https://doi.org/10.1007/978-3-030-94583-1_1">10.1007/978-3-030-94583-1_1</a>.
  short: E. Bartocci, T. Ferrere, T.A. Henzinger, D. Nickovic, A.O. Da Costa, in:,
    Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial
    Intelligence and Lecture Notes in Bioinformatics), Springer Nature, 2022, pp.
    1–19.
conference:
  end_date: 2022-01-18
  location: Philadelphia, PA, United States
  name: 'VMCAI: Verifcation, Model Checking, and Abstract Interpretation'
  start_date: 2022-01-16
date_created: 2022-02-20T23:01:34Z
date_published: 2022-01-14T00:00:00Z
date_updated: 2026-04-16T09:13:43Z
day: '14'
department:
- _id: ToHe
doi: 10.1007/978-3-030-94583-1_1
external_id:
  arxiv:
  - '2105.02013'
  isi:
  - '001059208500001'
intvolume: '     13182'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: ' https://doi.org/10.48550/arXiv.2105.02013'
month: '01'
oa: 1
oa_version: Preprint
page: 1-19
project:
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
publication: Lecture Notes in Computer Science (including subseries Lecture Notes
  in Artificial Intelligence and Lecture Notes in Bioinformatics)
publication_identifier:
  eisbn:
  - '9783030945831'
  eissn:
  - 1611-3349
  isbn:
  - '9783030945824'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Flavors of sequential information flow
type: conference
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 13182
year: '2022'
...
---
OA_place: publisher
_id: '11362'
abstract:
- lang: eng
  text: "Deep learning has enabled breakthroughs in challenging computing problems
    and has emerged as the standard problem-solving tool for computer vision and natural
    language processing tasks.\r\nOne exception to this trend is safety-critical tasks
    where robustness and resilience requirements contradict the black-box nature of
    neural networks. \r\nTo deploy deep learning methods for these tasks, it is vital
    to provide guarantees on neural network agents' safety and robustness criteria.
    \r\nThis can be achieved by developing formal verification methods to verify the
    safety and robustness properties of neural networks.\r\n\r\nOur goal is to design,
    develop and assess safety verification methods for neural networks to improve
    their reliability and trustworthiness in real-world applications.\r\nThis thesis
    establishes techniques for the verification of compressed and adversarially trained
    models as well as the design of novel neural networks for verifiably safe decision-making.\r\n\r\nFirst,
    we establish the problem of verifying quantized neural networks. Quantization
    is a technique that trades numerical precision for the computational efficiency
    of running a neural network and is widely adopted in industry.\r\nWe show that
    neglecting the reduced precision when verifying a neural network can lead to wrong
    conclusions about the robustness and safety of the network, highlighting that
    novel techniques for quantized network verification are necessary. We introduce
    several bit-exact verification methods explicitly designed for quantized neural
    networks and experimentally confirm on realistic networks that the network's robustness
    and other formal properties are affected by the quantization.\r\n\r\nFurthermore,
    we perform a case study providing evidence that adversarial training, a standard
    technique for making neural networks more robust, has detrimental effects on the
    network's performance. This robustness-accuracy tradeoff has been studied before
    regarding the accuracy obtained on classification datasets where each data point
    is independent of all other data points. On the other hand, we investigate the
    tradeoff empirically in robot learning settings where a both, a high accuracy
    and a high robustness, are desirable.\r\nOur results suggest that the negative
    side-effects of adversarial training outweigh its robustness benefits in practice.\r\n\r\nFinally,
    we consider the problem of verifying safety when running a Bayesian neural network
    policy in a feedback loop with systems over the infinite time horizon. Bayesian
    neural networks are probabilistic models for learning uncertainties in the data
    and are therefore often used on robotic and healthcare applications where data
    is inherently stochastic.\r\nWe introduce a method for recalibrating Bayesian
    neural networks so that they yield probability distributions over safe decisions
    only.\r\nOur method learns a safety certificate that guarantees safety over the
    infinite time horizon to determine which decisions are safe in every possible
    state of the system.\r\nWe demonstrate the effectiveness of our approach on a
    series of reinforcement learning benchmarks."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Mathias
  full_name: Lechner, Mathias
  id: 3DC22916-F248-11E8-B48F-1D18A9856A87
  last_name: Lechner
citation:
  ama: Lechner M. Learning verifiable representations. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11362">10.15479/at:ista:11362</a>
  apa: Lechner, M. (2022). <i>Learning verifiable representations</i>. Institute of
    Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11362">https://doi.org/10.15479/at:ista:11362</a>
  chicago: Lechner, Mathias. “Learning Verifiable Representations.” Institute of Science
    and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11362">https://doi.org/10.15479/at:ista:11362</a>.
  ieee: M. Lechner, “Learning verifiable representations,” Institute of Science and
    Technology Austria, 2022.
  ista: Lechner M. 2022. Learning verifiable representations. Institute of Science
    and Technology Austria.
  mla: Lechner, Mathias. <i>Learning Verifiable Representations</i>. Institute of
    Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11362">10.15479/at:ista:11362</a>.
  short: M. Lechner, Learning Verifiable Representations, Institute of Science and
    Technology Austria, 2022.
corr_author: '1'
date_created: 2022-05-12T07:14:01Z
date_published: 2022-05-12T00:00:00Z
date_updated: 2026-04-16T09:46:06Z
day: '12'
ddc:
- '004'
degree_awarded: PhD
department:
- _id: GradSch
- _id: ToHe
doi: 10.15479/at:ista:11362
ec_funded: 1
file:
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  file_size: 2732536
  relation: main_file
file_date_updated: 2022-05-17T15:19:39Z
has_accepted_license: '1'
keyword:
- neural networks
- verification
- machine learning
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: '124'
project:
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
- _id: 62781420-2b32-11ec-9570-8d9b63373d4d
  call_identifier: H2020
  grant_number: '101020093'
  name: Vigilant Algorithmic Monitoring of Software
publication_identifier:
  isbn:
  - 978-3-99078-017-6
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '11366'
    relation: part_of_dissertation
    status: public
  - id: '10665'
    relation: part_of_dissertation
    status: public
  - id: '10667'
    relation: part_of_dissertation
    status: public
  - id: '10666'
    relation: part_of_dissertation
    status: public
  - id: '7808'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000-0002-2985-7724
title: Learning verifiable representations
tmp:
  image: /image/cc_by_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nd/4.0/legalcode
  name: Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0)
  short: CC BY-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
_id: '10753'
abstract:
- lang: eng
  text: This is a comment on "Meta-learning synaptic plasticity and memory addressing
    for continual familiarity detection." Neuron. 2022 Feb 2;110(3):544-557.e8.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Basile J
  full_name: Confavreux, Basile J
  id: C7610134-B532-11EA-BD9F-F5753DDC885E
  last_name: Confavreux
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
citation:
  ama: 'Confavreux BJ, Vogels TP. A familiar thought: Machines that replace us? <i>Neuron</i>.
    2022;110(3):361-362. doi:<a href="https://doi.org/10.1016/j.neuron.2022.01.014">10.1016/j.neuron.2022.01.014</a>'
  apa: 'Confavreux, B. J., &#38; Vogels, T. P. (2022). A familiar thought: Machines
    that replace us? <i>Neuron</i>. Elsevier. <a href="https://doi.org/10.1016/j.neuron.2022.01.014">https://doi.org/10.1016/j.neuron.2022.01.014</a>'
  chicago: 'Confavreux, Basile J, and Tim P Vogels. “A Familiar Thought: Machines
    That Replace Us?” <i>Neuron</i>. Elsevier, 2022. <a href="https://doi.org/10.1016/j.neuron.2022.01.014">https://doi.org/10.1016/j.neuron.2022.01.014</a>.'
  ieee: 'B. J. Confavreux and T. P. Vogels, “A familiar thought: Machines that replace
    us?,” <i>Neuron</i>, vol. 110, no. 3. Elsevier, pp. 361–362, 2022.'
  ista: 'Confavreux BJ, Vogels TP. 2022. A familiar thought: Machines that replace
    us? Neuron. 110(3), 361–362.'
  mla: 'Confavreux, Basile J., and Tim P. Vogels. “A Familiar Thought: Machines That
    Replace Us?” <i>Neuron</i>, vol. 110, no. 3, Elsevier, 2022, pp. 361–62, doi:<a
    href="https://doi.org/10.1016/j.neuron.2022.01.014">10.1016/j.neuron.2022.01.014</a>.'
  short: B.J. Confavreux, T.P. Vogels, Neuron 110 (2022) 361–362.
corr_author: '1'
date_created: 2022-02-13T23:01:34Z
date_published: 2022-02-02T00:00:00Z
date_updated: 2026-06-18T08:47:45Z
day: '02'
ddc:
- '570'
department:
- _id: TiVo
doi: 10.1016/j.neuron.2022.01.014
external_id:
  isi:
  - '000751819100005'
  pmid:
  - '35114107'
intvolume: '       110'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.neuron.2022.01.014
month: '02'
oa: 1
oa_version: Published Version
page: 361-362
pmid: 1
publication: Neuron
publication_identifier:
  eissn:
  - 1097-4199
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'A familiar thought: Machines that replace us?'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 110
year: '2022'
...
---
_id: '11417'
abstract:
- lang: eng
  text: "Over the past few years, the field of quantum information science has seen
    tremendous progress toward realizing large-scale quantum computers. With demonstrations
    of quantum computers outperforming classical computers for a select range of problems,1–3
    we have finally entered the noisy, intermediate-scale quantum (NISQ) computing
    era. While the quantum computers of today are technological marvels, they are
    not yet error corrected, and it is unclear whether any system will scale beyond
    a few hundred logical qubits without significant changes to architecture and control
    schemes. Today's quantum systems are analogous to the ENIAC (Electronic Numerical
    Integrator And Computer) and EDVAC (Electronic Discrete Variable Automatic Computer)
    systems of the 1940s, which ran on vacuum tubes. These machines were built on
    a solid, nominally scalable architecture and when they were developed, nobody
    could have predicted the development of the transistor and the impact of the resulting
    semiconductor industry. Simply put, the computers of today are nothing like the
    early computers of the 1940s. We believe that the qubits of future fault-tolerant
    quantum systems will look quite different from the qubits of the NISQ machines
    in operation today. This Special Topic issue is devoted to new and emerging quantum
    systems with a focus on enabling technologies that can eventually lead to the
    quantum analog to the transistor. We have solicited both research4–18 and perspective
    articles19–21 to discuss new and emerging qubit systems with a focus on novel
    materials, encodings, and architectures. We are proud to present a collection
    that touches on a wide range of technologies including superconductors,7–13,21
    semiconductors,15–17,19 and individual atomic qubits.18\r\n"
acknowledgement: "We would like to thank all of the authors who contributed to\r\nthis
  Special Topic. We would also like to thank the editorial team at\r\nAPL including
  Jessica Trudeau, Emma Van Burns, Martin Weides,\r\nand Lesley Cohen."
article_number: '190401'
article_processing_charge: No
article_type: letter_note
author:
- first_name: Anthony J.
  full_name: Sigillito, Anthony J.
  last_name: Sigillito
- first_name: Jacob P.
  full_name: Covey, Jacob P.
  last_name: Covey
- first_name: Johannes M
  full_name: Fink, Johannes M
  id: 4B591CBA-F248-11E8-B48F-1D18A9856A87
  last_name: Fink
  orcid: 0000-0001-8112-028X
- first_name: Karl
  full_name: Petersson, Karl
  last_name: Petersson
- first_name: Stefan
  full_name: Preble, Stefan
  last_name: Preble
citation:
  ama: 'Sigillito AJ, Covey JP, Fink JM, Petersson K, Preble S. Emerging qubit systems:
    Guest editorial. <i>Applied Physics Letters</i>. 2022;120(19). doi:<a href="https://doi.org/10.1063/5.0097339">10.1063/5.0097339</a>'
  apa: 'Sigillito, A. J., Covey, J. P., Fink, J. M., Petersson, K., &#38; Preble,
    S. (2022). Emerging qubit systems: Guest editorial. <i>Applied Physics Letters</i>.
    American Institute of Physics. <a href="https://doi.org/10.1063/5.0097339">https://doi.org/10.1063/5.0097339</a>'
  chicago: 'Sigillito, Anthony J., Jacob P. Covey, Johannes M Fink, Karl Petersson,
    and Stefan Preble. “Emerging Qubit Systems: Guest Editorial.” <i>Applied Physics
    Letters</i>. American Institute of Physics, 2022. <a href="https://doi.org/10.1063/5.0097339">https://doi.org/10.1063/5.0097339</a>.'
  ieee: 'A. J. Sigillito, J. P. Covey, J. M. Fink, K. Petersson, and S. Preble, “Emerging
    qubit systems: Guest editorial,” <i>Applied Physics Letters</i>, vol. 120, no.
    19. American Institute of Physics, 2022.'
  ista: 'Sigillito AJ, Covey JP, Fink JM, Petersson K, Preble S. 2022. Emerging qubit
    systems: Guest editorial. Applied Physics Letters. 120(19), 190401.'
  mla: 'Sigillito, Anthony J., et al. “Emerging Qubit Systems: Guest Editorial.” <i>Applied
    Physics Letters</i>, vol. 120, no. 19, 190401, American Institute of Physics,
    2022, doi:<a href="https://doi.org/10.1063/5.0097339">10.1063/5.0097339</a>.'
  short: A.J. Sigillito, J.P. Covey, J.M. Fink, K. Petersson, S. Preble, Applied Physics
    Letters 120 (2022).
date_created: 2022-05-29T22:01:53Z
date_published: 2022-05-12T00:00:00Z
date_updated: 2026-06-18T17:14:33Z
day: '12'
ddc:
- '530'
department:
- _id: JoFi
doi: 10.1063/5.0097339
external_id:
  isi:
  - '000796002100002'
intvolume: '       120'
isi: 1
issue: '19'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1063/5.0097339
month: '05'
oa: 1
oa_version: Published Version
publication: Applied Physics Letters
publication_identifier:
  issn:
  - 0003-6951
publication_status: published
publisher: American Institute of Physics
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Emerging qubit systems: Guest editorial'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 120
year: '2022'
...
---
OA_place: publisher
_id: '11626'
abstract:
- lang: eng
  text: Plant growth and development is well known to be both, flexible and dynamic.
    The high capacity for post-embryonic organ formation and tissue regeneration requires
    tightly regulated intercellular communication and coordinated tissue polarization.
    One of the most important drivers for patterning and polarity in plant development
    is the phytohormone auxin. Auxin has the unique characteristic to establish polarized
    channels for its own active directional cell to cell transport. This fascinating
    phenomenon is called auxin canalization. Those auxin transport channels are characterized
    by the expression and polar, subcellular localization of PIN auxin efflux carriers.
    PIN proteins have the ability to dynamically change their localization and auxin
    itself can affect this by interfering with trafficking. Most of the underlying
    molecular mechanisms of canalization still remain enigmatic. What is known so
    far is that canonical auxin signaling is indispensable but also other non-canonical
    signaling components are thought to play a role. In order to shed light into the
    mysteries auf auxin canalization this study revisits the branches of auxin signaling
    in detail. Further a new auxin analogue, PISA, is developed which triggers auxin-like
    responses but does not directly activate canonical transcriptional auxin signaling.
    We revisit the direct auxin effect on PIN trafficking where we found that, contradictory
    to previous observations, auxin is very specifically promoting endocytosis of
    PIN2 but has no overall effect on endocytosis. Further, we evaluate which cellular
    processes related to PIN subcellular dynamics are involved in the establishment
    of auxin conducting channels and the formation of vascular tissue. We are re-evaluating
    the function of AUXIN BINDING PROTEIN 1 (ABP1) and provide a comprehensive picture
    about its developmental phneotypes and involvement in auxin signaling and canalization.
    Lastly, we are focusing on the crosstalk between the hormone strigolactone (SL)
    and auxin and found that SL is interfering with essentially all processes involved
    in auxin canalization in a non-transcriptional manner. Lastly we identify a new
    way of SL perception and signaling which is emanating from mitochondria, is independent
    of canonical SL signaling and is modulating primary root growth.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Michelle C
  full_name: Gallei, Michelle C
  id: 35A03822-F248-11E8-B48F-1D18A9856A87
  last_name: Gallei
  orcid: 0000-0003-1286-7368
citation:
  ama: Gallei MC. Auxin and strigolactone non-canonical signaling regulating development
    in Arabidopsis thaliana. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11626">10.15479/at:ista:11626</a>
  apa: Gallei, M. C. (2022). <i>Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana</i>. Institute of Science and Technology Austria.
    <a href="https://doi.org/10.15479/at:ista:11626">https://doi.org/10.15479/at:ista:11626</a>
  chicago: Gallei, Michelle C. “Auxin and Strigolactone Non-Canonical Signaling Regulating
    Development in Arabidopsis Thaliana.” Institute of Science and Technology Austria,
    2022. <a href="https://doi.org/10.15479/at:ista:11626">https://doi.org/10.15479/at:ista:11626</a>.
  ieee: M. C. Gallei, “Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana,” Institute of Science and Technology Austria,
    2022.
  ista: Gallei MC. 2022. Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana. Institute of Science and Technology Austria.
  mla: Gallei, Michelle C. <i>Auxin and Strigolactone Non-Canonical Signaling Regulating
    Development in Arabidopsis Thaliana</i>. Institute of Science and Technology Austria,
    2022, doi:<a href="https://doi.org/10.15479/at:ista:11626">10.15479/at:ista:11626</a>.
  short: M.C. Gallei, Auxin and Strigolactone Non-Canonical Signaling Regulating Development
    in Arabidopsis Thaliana, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-07-20T11:21:53Z
date_published: 2022-07-20T00:00:00Z
date_updated: 2026-06-18T19:02:05Z
day: '20'
ddc:
- '575'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JiFr
doi: 10.15479/at:ista:11626
ec_funded: 1
file:
- access_level: open_access
  checksum: bd7ac35403cf5b4b2607287d2a104b3a
  content_type: application/pdf
  creator: mgallei
  date_created: 2022-07-25T09:08:47Z
  date_updated: 2022-07-25T09:08:47Z
  file_id: '11645'
  file_name: Thesis_Gallei.pdf
  file_size: 9730864
  relation: main_file
- access_level: closed
  checksum: a9e54fe5471ba25dc13c2150c1b8ccbb
  content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
  creator: mgallei
  date_created: 2022-07-25T09:09:09Z
  date_updated: 2022-07-25T09:39:58Z
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  content_type: application/pdf
  creator: mgallei
  date_created: 2022-07-25T09:09:32Z
  date_updated: 2022-07-25T09:39:58Z
  description: This is the print version of the thesis including the full appendix
  file_id: '11647'
  file_name: Thesis_Gallei_to_print.pdf
  file_size: 24542837
  relation: source_file
- access_level: open_access
  checksum: f24acd3c0d864f4c6676e8b0d7bfa76b
  content_type: application/pdf
  creator: mgallei
  date_created: 2022-07-25T11:48:45Z
  date_updated: 2022-07-25T11:48:45Z
  file_id: '11650'
  file_name: Thesis_Gallei_Appendix.pdf
  file_size: 15435966
  relation: main_file
file_date_updated: 2022-07-25T11:48:45Z
has_accepted_license: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: '248'
project:
- _id: 261099A6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '742985'
  name: Tracing Evolution of Auxin Transport and Polarity in Plants
publication_identifier:
  isbn:
  - 978-3-99078-019-0
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '8138'
    relation: part_of_dissertation
    status: public
  - id: '7142'
    relation: part_of_dissertation
    status: public
  - id: '10411'
    relation: part_of_dissertation
    status: public
  - id: '8931'
    relation: part_of_dissertation
    status: public
  - id: '7465'
    relation: part_of_dissertation
    status: public
  - id: '9287'
    relation: part_of_dissertation
    status: public
  - id: '6260'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Eilon
  full_name: Shani, Eilon
  last_name: Shani
title: Auxin and strigolactone non-canonical signaling regulating development in Arabidopsis
  thaliana
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '10759'
abstract:
- lang: eng
  text: In this Thesis, I study composite quantum impurities with variational techniques,
    both inspired by machine learning as well as fully analytic. I supplement this
    with exploration of other applications of machine learning, in particular artificial
    neural networks, in many-body physics. In Chapters 3 and 4, I study quasiparticle
    systems with variational approach. I derive a Hamiltonian describing the angulon
    quasiparticle in the presence of a magnetic field. I apply analytic variational
    treatment to this Hamiltonian. Then, I introduce a variational approach for non-additive
    systems, based on artificial neural networks. I exemplify this approach on the
    example of the polaron quasiparticle (Fröhlich Hamiltonian). In Chapter 5, I continue
    using artificial neural networks, albeit in a different setting. I apply artificial
    neural networks to detect phases from snapshots of two types physical systems.
    Namely, I study Monte Carlo snapshots of multilayer classical spin models as well
    as molecular dynamics maps of colloidal systems. The main type of networks that
    I use here are convolutional neural networks, known for their applicability to
    image data.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Wojciech
  full_name: Rzadkowski, Wojciech
  id: 48C55298-F248-11E8-B48F-1D18A9856A87
  last_name: Rzadkowski
  orcid: 0000-0002-1106-4419
citation:
  ama: Rzadkowski W. Analytic and machine learning approaches to composite quantum
    impurities. 2022. doi:<a href="https://doi.org/10.15479/at:ista:10759">10.15479/at:ista:10759</a>
  apa: Rzadkowski, W. (2022). <i>Analytic and machine learning approaches to composite
    quantum impurities</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:10759">https://doi.org/10.15479/at:ista:10759</a>
  chicago: Rzadkowski, Wojciech. “Analytic and Machine Learning Approaches to Composite
    Quantum Impurities.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:10759">https://doi.org/10.15479/at:ista:10759</a>.
  ieee: W. Rzadkowski, “Analytic and machine learning approaches to composite quantum
    impurities,” Institute of Science and Technology Austria, 2022.
  ista: Rzadkowski W. 2022. Analytic and machine learning approaches to composite
    quantum impurities. Institute of Science and Technology Austria.
  mla: Rzadkowski, Wojciech. <i>Analytic and Machine Learning Approaches to Composite
    Quantum Impurities</i>. Institute of Science and Technology Austria, 2022, doi:<a
    href="https://doi.org/10.15479/at:ista:10759">10.15479/at:ista:10759</a>.
  short: W. Rzadkowski, Analytic and Machine Learning Approaches to Composite Quantum
    Impurities, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-02-16T13:27:37Z
date_published: 2022-02-21T00:00:00Z
date_updated: 2026-06-18T19:29:09Z
day: '21'
ddc:
- '530'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MiLe
doi: 10.15479/at:ista:10759
ec_funded: 1
file:
- access_level: closed
  checksum: 0fc54ad1eaede879c665ac9b53c93e22
  content_type: application/zip
  creator: wrzadkow
  date_created: 2022-02-21T13:58:16Z
  date_updated: 2022-02-22T07:20:12Z
  file_id: '10785'
  file_name: Rzadkowski_thesis_final_source.zip
  file_size: 17668233
  relation: source_file
- access_level: open_access
  checksum: 22d2d7af37ca31f6b1730c26cac7bced
  content_type: application/pdf
  creator: wrzadkow
  date_created: 2022-02-21T14:02:54Z
  date_updated: 2022-02-21T14:02:54Z
  file_id: '10786'
  file_name: Rzadkowski_thesis_final.pdf
  file_size: 13307331
  relation: main_file
  success: 1
file_date_updated: 2022-02-22T07:20:12Z
has_accepted_license: '1'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: '120'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '10762'
    relation: part_of_dissertation
    status: public
  - id: '415'
    relation: part_of_dissertation
    status: public
  - id: '8644'
    relation: part_of_dissertation
    status: public
  - id: '7956'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Mikhail
  full_name: Lemeshko, Mikhail
  id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
  last_name: Lemeshko
  orcid: 0000-0002-6990-7802
title: Analytic and machine learning approaches to composite quantum impurities
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12368'
abstract:
- lang: eng
  text: "Metazoan development relies on the formation and remodeling of cell-cell
    contacts. The \r\nbinding of adhesion receptors and remodeling of the actomyosin
    cell cortex at cell-cell \r\ninteraction sites have been implicated in cell-cell
    contact formation. Yet, how these two \r\nprocesses functionally interact to drive
    cell-cell contact expansion and strengthening \r\nremains unclear. Here, we study
    how primary germ layer progenitor cells from zebrafish \r\nbind to supported lipid
    bilayers (SLB) functionalized with E-cadherin ectodomains as an \r\nassay system
    for monitoring cell-cell contact formation at high spatiotemporal resolution.
    \r\nWe show that cell-cell contact formation represents a two-tiered process:
    E-cadherin\x02mediated downregulation of the small GTPase RhoA at the forming
    contact leads to both \r\ndepletion of Myosin-2 and decrease of F-actin. This
    is followed by centrifugal actin \r\nnetwork flows at the contact triggered by
    a sharp gradient of Myosin-2 at the rim of the \r\ncontact zone, with Myosin-2
    displaying higher cortical localization outside than inside of \r\nthe contact.
    These centrifugal cortical actin flows, in turn, not only further dilute the actin
    \r\nnetwork at the contact disc, but also lead to an accumulation of both F-actin
    and E\x02cadherin at the contact rim. Eventually, this combination of actomyosin
    downregulation \r\nand flows at the contact contribute to the characteristic molecular
    organization implicated \r\nin contact formation and maintenance: depletion of
    cortical actomyosin at the contact disc, \r\ndriving contact expansion by lowering
    interfacial tension at the contact, and accumulation \r\nof both E-cadherin and
    F-actin at the contact rim, mechanically linking the contractile \r\ncortices
    of the adhering cells. Thus, using a biomimetic assay, we exemplify how \r\nadhesion
    signaling and cell mechanics function together to modulate the spatial \r\norganization
    of cell-cell contacts."
acknowledged_ssus:
- _id: LifeSc
- _id: Bio
- _id: NanoFab
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Feyza N
  full_name: Arslan, Feyza N
  id: 49DA7910-F248-11E8-B48F-1D18A9856A87
  last_name: Arslan
  orcid: 0000-0001-5809-9566
citation:
  ama: Arslan FN. Remodeling of E-cadherin-mediated contacts via cortical  flows.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:12153">10.15479/at:ista:12153</a>
  apa: Arslan, F. N. (2022). <i>Remodeling of E-cadherin-mediated contacts via cortical 
    flows</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:12153">https://doi.org/10.15479/at:ista:12153</a>
  chicago: Arslan, Feyza N. “Remodeling of E-Cadherin-Mediated Contacts via Cortical 
    Flows.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:12153">https://doi.org/10.15479/at:ista:12153</a>.
  ieee: F. N. Arslan, “Remodeling of E-cadherin-mediated contacts via cortical  flows,”
    Institute of Science and Technology Austria, 2022.
  ista: Arslan FN. 2022. Remodeling of E-cadherin-mediated contacts via cortical 
    flows. Institute of Science and Technology Austria.
  mla: Arslan, Feyza N. <i>Remodeling of E-Cadherin-Mediated Contacts via Cortical 
    Flows</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:12153">10.15479/at:ista:12153</a>.
  short: F.N. Arslan, Remodeling of E-Cadherin-Mediated Contacts via Cortical  Flows,
    Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2023-01-25T10:43:24Z
date_published: 2022-09-29T00:00:00Z
date_updated: 2026-06-18T19:47:50Z
day: '29'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: CaHe
doi: 10.15479/at:ista:12153
ec_funded: 1
file:
- access_level: open_access
  checksum: e54a3e69b83ebf166544164afd25608e
  content_type: application/pdf
  creator: cchlebak
  date_created: 2023-01-25T10:52:46Z
  date_updated: 2023-01-25T10:52:46Z
  file_id: '12369'
  file_name: THESIS_FINAL_FArslan_pdfa.pdf
  file_size: 14581024
  relation: main_file
  success: 1
file_date_updated: 2023-01-25T10:52:46Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '113'
project:
- _id: 260F1432-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '742573'
  name: Interaction and feedback between cell mechanics and fate specification in
    vertebrate gastrulation
publication_identifier:
  isbn:
  - '978-3-99078-025-1 '
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '9350'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
title: Remodeling of E-cadherin-mediated contacts via cortical  flows
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12358'
abstract:
- lang: eng
  text: "The complex yarn structure of knitted and woven fabrics gives rise to both
    a mechanical and\r\nvisual complexity. The small-scale interactions of yarns colliding
    with and pulling on each\r\nother result in drastically different large-scale
    stretching and bending behavior, introducing\r\nanisotropy, curling, and more.
    While simulating cloth as individual yarns can reproduce this\r\ncomplexity and
    match the quality of real fabric, it may be too computationally expensive for\r\nlarge
    fabrics. On the other hand, continuum-based approaches do not need to discretize
    the\r\ncloth at a stitch-level, but it is non-trivial to find a material model
    that would replicate the\r\nlarge-scale behavior of yarn fabrics, and they discard
    the intricate visual detail. In this thesis,\r\nwe discuss three methods to try
    and bridge the gap between small-scale and large-scale yarn\r\nmechanics using
    numerical homogenization: fitting a continuum model to periodic yarn simulations,
    adding mechanics-aware yarn detail onto thin-shell simulations, and quantitatively\r\nfitting
    yarn parameters to physical measurements of real fabric.\r\nTo start, we present
    a method for animating yarn-level cloth effects using a thin-shell solver.\r\nWe
    first use a large number of periodic yarn-level simulations to build a model of
    the potential\r\nenergy density of the cloth, and then use it to compute forces
    in a thin-shell simulator. The\r\nresulting simulations faithfully reproduce expected
    effects like the stiffening of woven fabrics\r\nand the highly deformable nature
    and anisotropy of knitted fabrics at a fraction of the cost of\r\nfull yarn-level
    simulation.\r\nWhile our thin-shell simulations are able to capture large-scale
    yarn mechanics, they lack\r\nthe rich visual detail of yarn-level simulations.
    Therefore, we propose a method to animate\r\nyarn-level cloth geometry on top
    of an underlying deforming mesh in a mechanics-aware\r\nfashion in real time.
    Using triangle strains to interpolate precomputed yarn geometry, we are\r\nable
    to reproduce effects such as knit loops tightening under stretching at negligible
    cost.\r\nFinally, we introduce a methodology for inverse-modeling of yarn-level
    mechanics of cloth,\r\nbased on the mechanical response of fabrics in the real
    world. We compile a database from\r\nphysical tests of several knitted fabrics
    used in the textile industry spanning diverse physical\r\nproperties like stiffness,
    nonlinearity, and anisotropy. We then develop a system for approximating these
    mechanical responses with yarn-level cloth simulation, using homogenized\r\nshell
    models to speed up computation and adding some small-but-necessary extensions
    to\r\nyarn-level models used in computer graphics.\r\n"
acknowledged_ssus:
- _id: SSU
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Georg
  full_name: Sperl, Georg
  id: 4DD40360-F248-11E8-B48F-1D18A9856A87
  last_name: Sperl
citation:
  ama: 'Sperl G. Homogenizing yarn simulations: Large-scale mechanics, small-scale
    detail, and quantitative fitting. 2022. doi:<a href="https://doi.org/10.15479/at:ista:12103">10.15479/at:ista:12103</a>'
  apa: 'Sperl, G. (2022). <i>Homogenizing yarn simulations: Large-scale mechanics,
    small-scale detail, and quantitative fitting</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:12103">https://doi.org/10.15479/at:ista:12103</a>'
  chicago: 'Sperl, Georg. “Homogenizing Yarn Simulations: Large-Scale Mechanics, Small-Scale
    Detail, and Quantitative Fitting.” Institute of Science and Technology Austria,
    2022. <a href="https://doi.org/10.15479/at:ista:12103">https://doi.org/10.15479/at:ista:12103</a>.'
  ieee: 'G. Sperl, “Homogenizing yarn simulations: Large-scale mechanics, small-scale
    detail, and quantitative fitting,” Institute of Science and Technology Austria,
    2022.'
  ista: 'Sperl G. 2022. Homogenizing yarn simulations: Large-scale mechanics, small-scale
    detail, and quantitative fitting. Institute of Science and Technology Austria.'
  mla: 'Sperl, Georg. <i>Homogenizing Yarn Simulations: Large-Scale Mechanics, Small-Scale
    Detail, and Quantitative Fitting</i>. Institute of Science and Technology Austria,
    2022, doi:<a href="https://doi.org/10.15479/at:ista:12103">10.15479/at:ista:12103</a>.'
  short: 'G. Sperl, Homogenizing Yarn Simulations: Large-Scale Mechanics, Small-Scale
    Detail, and Quantitative Fitting, Institute of Science and Technology Austria,
    2022.'
corr_author: '1'
date_created: 2023-01-24T10:49:46Z
date_published: 2022-09-22T00:00:00Z
date_updated: 2026-06-18T19:57:47Z
day: '22'
ddc:
- '000'
- '620'
degree_awarded: PhD
department:
- _id: GradSch
- _id: ChWo
doi: 10.15479/at:ista:12103
ec_funded: 1
file:
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  date_updated: 2023-02-02T09:29:57Z
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file_date_updated: 2023-02-02T09:39:25Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '138'
project:
- _id: 2533E772-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '638176'
  name: 'Big Splash: Efficient Simulation of Natural Phenomena at Extremely Large
    Scales'
publication_identifier:
  isbn:
  - 978-3-99078-020-6
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
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    relation: part_of_dissertation
    status: public
  - id: '11736'
    relation: part_of_dissertation
    status: public
  - id: '9818'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Christopher J
  full_name: Wojtan, Christopher J
  id: 3C61F1D2-F248-11E8-B48F-1D18A9856A87
  last_name: Wojtan
  orcid: 0000-0001-6646-5546
title: 'Homogenizing yarn simulations: Large-scale mechanics, small-scale detail,
  and quantitative fitting'
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11879'
abstract:
- lang: eng
  text: "As the overall global mean surface temperature is increasing due to climate
    change, plant\r\nadaptation to those stressful conditions is of utmost importance
    for their survival. Plants are\r\nsessile organisms, thus to compensate for their
    lack of mobility, they evolved a variety of\r\nmechanisms enabling them to flexibly
    adjust their physiological, growth and developmental\r\nprocesses to fluctuating
    temperatures and to survive in harsh environments. While these unique\r\nadaptation
    abilities provide an important evolutionary advantage, overall modulation of plant\r\ngrowth
    and developmental program due to non-optimal temperature negatively affects biomass\r\nproduction,
    crop productivity or sensitivity to pathogens. Thus, understanding molecular\r\nprocesses
    underlying plant adaptation to increased temperature can provide important\r\nresources
    for breeding strategies to ensure sufficient agricultural food production.\r\nAn
    increase in ambient temperature by a few degrees leads to profound changes in
    organ growth\r\nincluding enhanced hypocotyl elongation, expansion of petioles,
    hyponastic growth of leaves and\r\ncotyledons, collectively named thermomorphogenesis
    (Casal & Balasubramanian, 2019). Auxin,\r\none of the best-studied growth hormones,
    plays an essential role in this process by direct\r\nactivation of transcriptional
    and non-transcriptional processes resulting in elongation growth\r\n(Majda & Robert,
    2018).To modulate hypocotyl growth in response to high ambient temperature\r\n(hAT),
    auxin needs to be redistributed accordingly. PINs, auxin efflux transporters,
    are key\r\ncomponents of the polar auxin transport (PAT) machinery, which controls
    the amount and\r\ndirection of auxin translocated in the plant tissues and organs(Adamowski
    & Friml, 2015). Hence,\r\nPIN-mediated transport is tightly linked with thermo-morphogenesis,
    and interference with PAT\r\nthrough either chemical or genetic means dramatically
    affecting the adaptive responses to hAT.\r\nIntriguingly, despite the key role
    of PIN mediated transport in growth response to hAT, whether\r\nand how PINs at
    the level of expression adapt to fluctuation in temperature is scarcely\r\nunderstood.\r\nWith
    genetic, molecular and advanced bio-imaging approaches, we demonstrate the role
    of PIN\r\nauxin transporters in the regulation of hypocotyl growth in response
    to hAT. We show that via\r\nadjustment of PIN3, PIN4 and PIN7 expression in cotyledons
    and hypocotyls, auxin distribution is modulated thereby determining elongation
    pattern of epidermal cells at hAT. Furthermore, we\r\nidentified three Zinc-Finger
    (ZF) transcription factors as novel molecular components of the\r\nthermo-regulatory
    network, which through negative regulation of PIN transcription adjust the\r\ntransport
    of auxin at hAT. Our results suggest that the ZF-PIN module might be a part of
    the\r\nnegative feedback loop attenuating the activity of the thermo-sensing pathway
    to restrain\r\nexaggerated growth and developmental responses to hAT."
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: SSU
acknowledgement: I would like to acknowledge ISTA and all the people from the Scientific
  Service Units and at ISTA, in particular Dorota Jaworska for excellent technical
  and scientific support as well as ÖAW for funding my research for over 3 years (DOC
  ÖAW Fellowship PR1022OEAW02).
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Christina
  full_name: Artner, Christina
  id: 45DF286A-F248-11E8-B48F-1D18A9856A87
  last_name: Artner
citation:
  ama: Artner C. Modulation of auxin transport via ZF proteins adjust plant response
    to high ambient temperature. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11879">10.15479/at:ista:11879</a>
  apa: Artner, C. (2022). <i>Modulation of auxin transport via ZF proteins adjust
    plant response to high ambient temperature</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:11879">https://doi.org/10.15479/at:ista:11879</a>
  chicago: Artner, Christina. “Modulation of Auxin Transport via ZF Proteins Adjust
    Plant Response to High Ambient Temperature.” Institute of Science and Technology
    Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11879">https://doi.org/10.15479/at:ista:11879</a>.
  ieee: C. Artner, “Modulation of auxin transport via ZF proteins adjust plant response
    to high ambient temperature,” Institute of Science and Technology Austria, 2022.
  ista: Artner C. 2022. Modulation of auxin transport via ZF proteins adjust plant
    response to high ambient temperature. Institute of Science and Technology Austria.
  mla: Artner, Christina. <i>Modulation of Auxin Transport via ZF Proteins Adjust
    Plant Response to High Ambient Temperature</i>. Institute of Science and Technology
    Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11879">10.15479/at:ista:11879</a>.
  short: C. Artner, Modulation of Auxin Transport via ZF Proteins Adjust Plant Response
    to High Ambient Temperature, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-08-17T07:58:53Z
date_published: 2022-08-17T00:00:00Z
date_updated: 2026-04-07T14:30:39Z
day: '17'
ddc:
- '580'
degree_awarded: PhD
department:
- _id: GradSch
- _id: EvBe
doi: 10.15479/at:ista:11879
file:
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  checksum: a2c2fdc28002538840490bfa6a08b2cb
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  creator: cartner
  date_created: 2022-08-17T12:08:49Z
  date_updated: 2023-09-09T22:30:03Z
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  date_updated: 2023-09-09T22:30:03Z
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  file_name: ChristinaArtner_PhD_Thesis_2022.7z
  file_size: 19097730
  relation: source_file
file_date_updated: 2023-09-09T22:30:03Z
has_accepted_license: '1'
keyword:
- high ambient temperature
- auxin
- PINs
- Zinc-Finger proteins
- thermomorphogenesis
- stress
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: '128'
project:
- _id: 2685A872-B435-11E9-9278-68D0E5697425
  name: Hormonal regulation of plant adaptive responses to environmental signals
publication_identifier:
  isbn:
  - 978-3-99078-022-0
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
title: Modulation of auxin transport via ZF proteins adjust plant response to high
  ambient temperature
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11393'
abstract:
- lang: eng
  text: "AMPA receptors (AMPARs) mediate fast excitatory neurotransmission and their
    role is\r\nimplicated in complex processes such as learning and memory and various
    neurological\r\ndiseases. These receptors are composed of different subunits and
    the subunit composition can\r\naffect channel properties, receptor trafficking
    and interaction with other associated proteins.\r\nUsing the high sensitivity
    SDS-digested freeze-fracture replica labeling (SDS-FRL) for\r\nelectron microscopy
    I investigated the number, density, and localization of AMPAR subunits,\r\nGluA1,
    GluA2, GluA3, and GluA1-3 (panAMPA) in pyramidal cells in the CA1 area of mouse\r\nhippocampus.
    I have found that the immunogold labeling for all of these subunits in the\r\npostsynaptic
    sites was highest in stratum radiatum and lowest in stratum lacunosummoleculare.
    The labeling density for the all subunits in the extrasynaptic sites showed a
    gradual\r\nincrease from the pyramidal cell soma towards the distal part of stratum
    radiatum. The densities\r\nof extrasynaptic GluA1, GluA2 and panAMPA labeling
    reached 10-15% of synaptic densities,\r\nwhile the ratio of extrasynaptic labeling
    for GluA3 was significantly lower compared than those\r\nfor other subunits. The
    labeling patterns for GluA1, GluA2 and GluA1-3 are similar and their\r\ndensities
    were higher in the periphery than center of synapses. In contrast, the GluA3-\r\ncontaining
    receptors were more centrally localized compared to the GluA1- and GluA2-\r\ncontaining
    receptors.\r\nThe hippocampus plays a central role in learning and memory. Contextual
    learning has been\r\nshown to require the delivery of AMPA receptors to CA1 synapses
    in the dorsal hippocampus.\r\nHowever, proximodistal heterogeneity of this plasticity
    and particular contribution of different\r\nAMPA receptor subunits are not fully
    understood. By combining inhibitory avoidance task, a\r\nhippocampus-dependent
    contextual fear-learning paradigm, with SDS-FRL, I have revealed an\r\nincrease
    in synaptic density specific to GluA1-containing AMPA receptors in the CA1 area.\r\nThe
    intrasynaptic distribution of GluA1 also changed from the periphery to center-preferred\r\npattern.
    Furthermore, this synaptic plasticity was evident selectively in stratum radiatum
    but\r\nnot stratum oriens, and in the CA1 subregion proximal but not distal to
    CA2. These findings\r\nfurther contribute to our understanding of how specific
    hippocampal subregions and AMPA\r\nreceptor subunits are involved in physiological
    learning.\r\nAlthough the immunolabeling results above shed light on subunit-specific
    plasticity in\r\nAMPAR distribution, no tools to visualize and study the subunit
    composition at the single\r\nchannel level in situ have been available. Electron
    microscopy with conventional immunogold\r\nlabeling approaches has limitations
    in the single channel analysis because of the large size of\r\nantibodies and
    steric hindrance hampering multiple subunit labeling of single channels. I\r\nmanaged
    to develop a new chemical labeling system using a short peptide tag and small\r\nsynthetic
    probes, which form specific covalent bond with a cysteine residue in the tag fused
    to\r\nproteins of interest (reactive tag system). I additionally made substantial
    progress into adapting\r\nthis system for AMPA receptor subunits."
acknowledged_ssus:
- _id: EM-Fac
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Marijo
  full_name: Jevtic, Marijo
  id: 4BE3BC94-F248-11E8-B48F-1D18A9856A87
  last_name: Jevtic
citation:
  ama: Jevtic M. Contextual fear learning induced changes in AMPA receptor subtypes
    along the proximodistal axis in dorsal hippocampus. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11393">10.15479/at:ista:11393</a>
  apa: Jevtic, M. (2022). <i>Contextual fear learning induced changes in AMPA receptor
    subtypes along the proximodistal axis in dorsal hippocampus</i>. Institute of
    Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11393">https://doi.org/10.15479/at:ista:11393</a>
  chicago: Jevtic, Marijo. “Contextual Fear Learning Induced Changes in AMPA Receptor
    Subtypes along the Proximodistal Axis in Dorsal Hippocampus.” Institute of Science
    and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11393">https://doi.org/10.15479/at:ista:11393</a>.
  ieee: M. Jevtic, “Contextual fear learning induced changes in AMPA receptor subtypes
    along the proximodistal axis in dorsal hippocampus,” Institute of Science and
    Technology Austria, 2022.
  ista: Jevtic M. 2022. Contextual fear learning induced changes in AMPA receptor
    subtypes along the proximodistal axis in dorsal hippocampus. Institute of Science
    and Technology Austria.
  mla: Jevtic, Marijo. <i>Contextual Fear Learning Induced Changes in AMPA Receptor
    Subtypes along the Proximodistal Axis in Dorsal Hippocampus</i>. Institute of
    Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11393">10.15479/at:ista:11393</a>.
  short: M. Jevtic, Contextual Fear Learning Induced Changes in AMPA Receptor Subtypes
    along the Proximodistal Axis in Dorsal Hippocampus, Institute of Science and Technology
    Austria, 2022.
corr_author: '1'
date_created: 2022-05-17T08:57:41Z
date_published: 2022-05-16T00:00:00Z
date_updated: 2026-04-07T14:31:19Z
day: '16'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: RySh
doi: 10.15479/at:ista:11393
file:
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  date_created: 2022-05-17T09:08:06Z
  date_updated: 2023-05-17T22:30:03Z
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file_date_updated: 2023-05-17T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: '108'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '7391'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
title: Contextual fear learning induced changes in AMPA receptor subtypes along the
  proximodistal axis in dorsal hippocampus
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12366'
abstract:
- lang: eng
  text: "Recent substantial advances in the feld of superconducting circuits have
    shown its\r\npotential as a leading platform for future quantum computing. In
    contrast to classical\r\ncomputers based on bits that are represented by a single
    binary value, 0 or 1, quantum\r\nbits (or qubits) can be in a superposition of
    both. Thus, quantum computers can store\r\nand handle more information at the
    same time and a quantum advantage has already\r\nbeen demonstrated for two types
    of computational tasks. Rapid progress in academic\r\nand industry labs accelerates
    the development of superconducting processors which may\r\nsoon fnd applications
    in complex computations, chemical simulations, cryptography, and\r\noptimization.
    Now that these machines are scaled up to tackle such problems the questions\r\nof
    qubit interconnects and networks becomes very relevant. How to route signals on-chip\r\nbetween
    diferent processor components? What is the most efcient way to entangle\r\nqubits?
    And how to then send and process entangled signals between distant cryostats\r\nhosting
    superconducting processors?\r\nIn this thesis, we are looking for solutions to
    these problems by studying the collective\r\nbehavior of superconducting qubit
    ensembles. We frst demonstrate on-demand tunable\r\ndirectional scattering of
    microwave photons from a pair of qubits in a waveguide. Such a\r\ndevice can route
    microwave photons on-chip with a high diode efciency. Then we focus\r\non studying
    ultra-strong coupling regimes between light (microwave photons) and matter\r\n(superconducting
    qubits), a regime that could be promising for extremely fast multi-qubit\r\nentanglement
    generation. Finally, we show coherent pulse storage and periodic revivals\r\nin
    a fve qubit ensemble strongly coupled to a resonator. Such a reconfgurable storage\r\ndevice
    could be used as part of a quantum repeater that is needed for longer-distance\r\nquantum
    communication.\r\nThe achieved high degree of control over multi-qubit ensembles
    highlights not only the\r\nbeautiful physics of circuit quantum electrodynamics,
    it also represents the frst step\r\ntoward new quantum simulation and communication
    methods, and certain techniques\r\nmay also fnd applications in future superconducting
    quantum computing hardware.\r\n"
acknowledged_ssus:
- _id: NanoFab
- _id: M-Shop
- _id: EM-Fac
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Elena
  full_name: Redchenko, Elena
  id: 2C21D6E8-F248-11E8-B48F-1D18A9856A87
  last_name: Redchenko
citation:
  ama: Redchenko E. Controllable states of superconducting Qubit ensembles. 2022.
    doi:<a href="https://doi.org/10.15479/at:ista:12132">10.15479/at:ista:12132</a>
  apa: Redchenko, E. (2022). <i>Controllable states of superconducting Qubit ensembles</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:12132">https://doi.org/10.15479/at:ista:12132</a>
  chicago: Redchenko, Elena. “Controllable States of Superconducting Qubit Ensembles.”
    Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:12132">https://doi.org/10.15479/at:ista:12132</a>.
  ieee: E. Redchenko, “Controllable states of superconducting Qubit ensembles,” Institute
    of Science and Technology Austria, 2022.
  ista: Redchenko E. 2022. Controllable states of superconducting Qubit ensembles.
    Institute of Science and Technology Austria.
  mla: Redchenko, Elena. <i>Controllable States of Superconducting Qubit Ensembles</i>.
    Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:12132">10.15479/at:ista:12132</a>.
  short: E. Redchenko, Controllable States of Superconducting Qubit Ensembles, Institute
    of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2023-01-25T09:17:02Z
date_published: 2022-09-26T00:00:00Z
date_updated: 2026-04-07T14:22:39Z
day: '26'
ddc:
- '530'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JoFi
doi: 10.15479/at:ista:12132
ec_funded: 1
file:
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  date_updated: 2023-01-26T23:30:44Z
  embargo: 2022-12-28
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file_date_updated: 2023-01-26T23:30:44Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '168'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 26336814-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '758053'
  name: A Fiber Optic Transceiver for Superconducting Qubits
- _id: 237CBA6C-32DE-11EA-91FC-C7463DDC885E
  call_identifier: H2020
  grant_number: '862644'
  name: Quantum readout techniques and technologies
publication_identifier:
  isbn:
  - 978-3-99078-024-4
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Johannes M
  full_name: Fink, Johannes M
  id: 4B591CBA-F248-11E8-B48F-1D18A9856A87
  last_name: Fink
  orcid: 0000-0001-8112-028X
title: Controllable states of superconducting Qubit ensembles
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11193'
abstract:
- lang: eng
  text: "The infiltration of immune cells into tissues underlies the establishment
    of tissue-resident\r\nmacrophages and responses to infections and tumors. However,
    the mechanisms immune\r\ncells utilize to collectively migrate through tissue
    barriers in vivo are not yet well understood.\r\nIn this thesis, I describe two
    mechanisms that Drosophila immune cells (hemocytes) use to\r\novercome the tissue
    barrier of the germband in the embryo. One strategy is the strengthening\r\nof
    the actin cortex through developmentally controlled transcriptional regulation
    induced by\r\nthe Drosophila proto-oncogene family member Dfos, which I show in
    Chapter 2. Dfos induces\r\nexpression of the tetraspanin TM4SF and the filamin
    Cher leading to higher levels of the\r\nactivated formin Dia at the cortex and
    increased cortical F-actin. This enhanced cortical\r\nstrength allows hemocytes
    to overcome the physical resistance of the surrounding tissue and\r\ntranslocate
    their nucleus to move forward. This mechanism affects the speed of migration\r\nwhen
    hemocytes face a confined environment in vivo.\r\nAnother aspect of the invasion
    process is the initial step of the leading hemocytes entering\r\nthe tissue, which
    potentially guides the follower cells. In Chapter 3, I describe a novel\r\nsubpopulation
    of hemocytes activated by BMP signaling prior to tissue invasion that leads\r\npenetration
    into the germband. Hemocytes that are deficient in BMP signaling activation\r\nshow
    impaired persistence at the tissue entry, while their migration speed remains\r\nunaffected.\r\nThis
    suggests that there might be different mechanisms controlling immune cell migration\r\nwithin
    the confined environment in vivo, one of these being the general ability to overcome\r\nthe
    resistance of the surrounding tissue and another affecting the order of hemocytes
    that\r\ncollectively invade the tissue in a stream of individual cells.\r\nTogether,
    my findings provide deeper insights into transcriptional changes in immune\r\ncells
    that enable efficient tissue invasion and pave the way for future studies investigating
    the\r\nearly colonization of tissues by macrophages in higher organisms. Moreover,
    they extend the\r\ncurrent view of Drosophila immune cell heterogeneity and point
    toward a potentially\r\nconserved role for canonical BMP signaling in specifying
    immune cells that lead the migration\r\nof tissue resident macrophages during
    embryogenesis."
acknowledged_ssus:
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Stephanie
  full_name: Wachner, Stephanie
  id: 2A95E7B0-F248-11E8-B48F-1D18A9856A87
  last_name: Wachner
citation:
  ama: Wachner S. Transcriptional regulation by Dfos and BMP-signaling support tissue
    invasion of Drosophila immune cells. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11193">10.15479/at:ista:11193</a>
  apa: Wachner, S. (2022). <i>Transcriptional regulation by Dfos and BMP-signaling
    support tissue invasion of Drosophila immune cells</i>. Institute of Science and
    Technology Austria. <a href="https://doi.org/10.15479/at:ista:11193">https://doi.org/10.15479/at:ista:11193</a>
  chicago: Wachner, Stephanie. “Transcriptional Regulation by Dfos and BMP-Signaling
    Support Tissue Invasion of Drosophila Immune Cells.” Institute of Science and
    Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11193">https://doi.org/10.15479/at:ista:11193</a>.
  ieee: S. Wachner, “Transcriptional regulation by Dfos and BMP-signaling support
    tissue invasion of Drosophila immune cells,” Institute of Science and Technology
    Austria, 2022.
  ista: Wachner S. 2022. Transcriptional regulation by Dfos and BMP-signaling support
    tissue invasion of Drosophila immune cells. Institute of Science and Technology
    Austria.
  mla: Wachner, Stephanie. <i>Transcriptional Regulation by Dfos and BMP-Signaling
    Support Tissue Invasion of Drosophila Immune Cells</i>. Institute of Science and
    Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11193">10.15479/at:ista:11193</a>.
  short: S. Wachner, Transcriptional Regulation by Dfos and BMP-Signaling Support
    Tissue Invasion of Drosophila Immune Cells, Institute of Science and Technology
    Austria, 2022.
corr_author: '1'
date_created: 2022-04-20T08:59:07Z
date_published: 2022-04-20T00:00:00Z
date_updated: 2026-04-07T14:24:19Z
day: '20'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: DaSi
doi: 10.15479/at:ista:11193
file:
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  creator: cchlebak
  date_created: 2022-04-20T09:03:57Z
  date_updated: 2023-04-21T22:30:03Z
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  date_created: 2022-04-22T12:41:00Z
  date_updated: 2023-04-21T22:30:03Z
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  file_id: '11329'
  file_name: Thesis_Stephanie_Wachner_20200414.zip
  file_size: 65864612
  relation: source_file
file_date_updated: 2023-04-21T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: '170'
project:
- _id: 26199CA4-B435-11E9-9278-68D0E5697425
  grant_number: '24800'
  name: Implications of a TGFÎ²/Dpp-activated subpopulation for Drosophila macrophage
    migration
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '10614'
    relation: part_of_dissertation
    status: public
  - id: '544'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Daria E
  full_name: Siekhaus, Daria E
  id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
  last_name: Siekhaus
  orcid: 0000-0001-8323-8353
title: Transcriptional regulation by Dfos and BMP-signaling support tissue invasion
  of Drosophila immune cells
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11388'
abstract:
- lang: eng
  text: "In evolve and resequence experiments, a population is sequenced, subjected
    to selection and\r\nthen sequenced again, so that genetic changes before and after
    selection can be observed at\r\nthe genetic level. Here, I use these studies to
    better understand the genetic basis of complex\r\ntraits - traits which depend
    on more than a few genes.\r\nIn the first chapter, I discuss the first evolve
    and resequence experiment, in which a population\r\nof mice, the so-called \"Longshanks\"
    mice, were selected for tibia length while their body mass\r\nwas kept constant.
    The full pedigree is known. We observed a selection response on all\r\nchromosomes
    and used the infinitesimal model with linkage, a model which assumes an infinite\r\nnumber
    of genes with infinitesimally small effect sizes, as a null model. Results implied
    a very\r\npolygenic basis with a few loci of major effect standing out and changing
    in parallel. There\r\nwas large variability between the different chromosomes
    in this study, probably due to LD.\r\nIn chapter two, I go on to discuss the impact
    of LD, on the variability in an allele-frequency\r\nbased summary statistic, giving
    an equation based on the initial allele frequencies, average\r\npairwise LD, and
    the first four moments of the haplotype block copy number distribution. I\r\ndescribe
    this distribution by referring back to the founder generation. I then demonstrate\r\nhow
    to infer selection via a maximum likelihood scheme on the example of a single
    locus and\r\ndiscuss how to extend this to more realistic scenarios.\r\nIn chapter
    three, I discuss the second evolve and resequence experiment, in which a small\r\npopulation
    of Drosophila melanogaster was selected for increased pupal case size over 6\r\ngenerations.
    The experiment was highly replicated with 27 lines selected within family and
    a\r\nknown pedigree. We observed a phenotypic selection response of over one standard
    deviation.\r\nI describe the patterns in allele frequency data, including allele
    frequency changes and patterns\r\nof heterozygosity, and give ideas for future
    work."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Stefanie
  full_name: Belohlavy, Stefanie
  id: 43FE426A-F248-11E8-B48F-1D18A9856A87
  last_name: Belohlavy
  orcid: 0000-0002-9849-498X
citation:
  ama: Belohlavy S. The genetic basis of complex traits studied via analysis of evolve
    and resequence experiments. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11388">10.15479/at:ista:11388</a>
  apa: Belohlavy, S. (2022). <i>The genetic basis of complex traits studied via analysis
    of evolve and resequence experiments</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:11388">https://doi.org/10.15479/at:ista:11388</a>
  chicago: Belohlavy, Stefanie. “The Genetic Basis of Complex Traits Studied via Analysis
    of Evolve and Resequence Experiments.” Institute of Science and Technology Austria,
    2022. <a href="https://doi.org/10.15479/at:ista:11388">https://doi.org/10.15479/at:ista:11388</a>.
  ieee: S. Belohlavy, “The genetic basis of complex traits studied via analysis of
    evolve and resequence experiments,” Institute of Science and Technology Austria,
    2022.
  ista: Belohlavy S. 2022. The genetic basis of complex traits studied via analysis
    of evolve and resequence experiments. Institute of Science and Technology Austria.
  mla: Belohlavy, Stefanie. <i>The Genetic Basis of Complex Traits Studied via Analysis
    of Evolve and Resequence Experiments</i>. Institute of Science and Technology
    Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11388">10.15479/at:ista:11388</a>.
  short: S. Belohlavy, The Genetic Basis of Complex Traits Studied via Analysis of
    Evolve and Resequence Experiments, Institute of Science and Technology Austria,
    2022.
corr_author: '1'
date_created: 2022-05-16T16:49:18Z
date_published: 2022-05-18T00:00:00Z
date_updated: 2026-04-07T14:29:57Z
day: '18'
ddc:
- '576'
degree_awarded: PhD
department:
- _id: GradSch
- _id: NiBa
doi: 10.15479/at:ista:11388
file:
- access_level: open_access
  checksum: 4d75e6a619df7e8a9d6e840aee182380
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  creator: sbelohla
  date_created: 2022-05-19T13:03:13Z
  date_updated: 2023-05-20T22:30:03Z
  embargo: 2023-05-19
  file_id: '11398'
  file_name: thesis_sb_final_pdfa.pdf
  file_size: 8247240
  relation: main_file
- access_level: closed
  checksum: 7a5d8b6dd0ca00784f860075b0a7d8f0
  content_type: application/x-zip-compressed
  creator: sbelohla
  date_created: 2022-05-19T13:07:47Z
  date_updated: 2023-05-20T22:30:03Z
  embargo_to: open_access
  file_id: '11399'
  file_name: thesis_sb_final.zip
  file_size: 7094
  relation: source_file
file_date_updated: 2023-05-20T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: '98'
publication_identifier:
  isbn:
  - 978-3-99078-018-3
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '6713'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
title: The genetic basis of complex traits studied via analysis of evolve and resequence
  experiments
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
_id: '10703'
abstract:
- lang: eng
  text: 'When crawling through the body, leukocytes often traverse tissues that are
    densely packed with extracellular matrix and other cells, and this raises the
    question: How do leukocytes overcome compressive mechanical loads? Here, we show
    that the actin cortex of leukocytes is mechanoresponsive and that this responsiveness
    requires neither force sensing via the nucleus nor adhesive interactions with
    a substrate. Upon global compression of the cell body as well as local indentation
    of the plasma membrane, Wiskott-Aldrich syndrome protein (WASp) assembles into
    dot-like structures, providing activation platforms for Arp2/3 nucleated actin
    patches. These patches locally push against the external load, which can be obstructing
    collagen fibers or other cells, and thereby create space to facilitate forward
    locomotion. We show in vitro and in vivo that this WASp function is rate limiting
    for ameboid leukocyte migration in dense but not in loose environments and is
    required for trafficking through diverse tissues such as skin and lymph nodes.'
acknowledged_ssus:
- _id: LifeSc
- _id: Bio
- _id: EM-Fac
acknowledgement: We thank N. Darwish-Miranda, F. Leite, F.P. Assen, and A. Eichner
  for advice and help with experiments. We thank J. Renkawitz, E. Kiermaier, A. Juanes
  Garcia, and M. Avellaneda for critical reading of the manuscript. We thank M. Driscoll
  for advice on fluorescent labeling of collagen gels. This research was supported
  by the Scientific Service Units (SSUs) of IST Austria through resources provided
  by Molecular Biology Services/Lab Support Facility (LSF)/Bioimaging Facility/Electron
  Microscopy Facility. This work was funded by grants from the European Research Council
  ( CoG 724373 ) and the Austrian Science Foundation (FWF) to M.S. F.G. received funding
  from the European Union’s Horizon 2020 research and innovation program under the
  Marie Skłodowska-Curie grant agreement no. 747687.
article_processing_charge: No
article_type: original
author:
- first_name: Florian
  full_name: Gaertner, Florian
  last_name: Gaertner
- first_name: Patricia
  full_name: Dos Reis Rodrigues, Patricia
  id: 26E95904-5160-11E9-9C0B-C5B0DC97E90F
  last_name: Dos Reis Rodrigues
  orcid: 0000-0003-1681-508X
- first_name: Ingrid
  full_name: De Vries, Ingrid
  id: 4C7D837E-F248-11E8-B48F-1D18A9856A87
  last_name: De Vries
- first_name: Miroslav
  full_name: Hons, Miroslav
  id: 4167FE56-F248-11E8-B48F-1D18A9856A87
  last_name: Hons
  orcid: 0000-0002-6625-3348
- first_name: Juan
  full_name: Aguilera, Juan
  last_name: Aguilera
- first_name: Michael
  full_name: Riedl, Michael
  id: 3BE60946-F248-11E8-B48F-1D18A9856A87
  last_name: Riedl
  orcid: 0000-0003-4844-6311
- first_name: Alexander F
  full_name: Leithner, Alexander F
  id: 3B1B77E4-F248-11E8-B48F-1D18A9856A87
  last_name: Leithner
  orcid: 0000-0002-1073-744X
- first_name: Saren
  full_name: Tasciyan, Saren
  id: 4323B49C-F248-11E8-B48F-1D18A9856A87
  last_name: Tasciyan
  orcid: 0000-0003-1671-393X
- first_name: Aglaja
  full_name: Kopf, Aglaja
  id: 31DAC7B6-F248-11E8-B48F-1D18A9856A87
  last_name: Kopf
  orcid: 0000-0002-2187-6656
- first_name: Jack
  full_name: Merrin, Jack
  id: 4515C308-F248-11E8-B48F-1D18A9856A87
  last_name: Merrin
  orcid: 0000-0001-5145-4609
- first_name: Vanessa
  full_name: Zheden, Vanessa
  id: 39C5A68A-F248-11E8-B48F-1D18A9856A87
  last_name: Zheden
  orcid: 0000-0002-9438-4783
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: Robert
  full_name: Hauschild, Robert
  id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
  last_name: Hauschild
  orcid: 0000-0001-9843-3522
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
citation:
  ama: Gaertner F, Dos Reis Rodrigues P, de Vries I, et al. WASp triggers mechanosensitive
    actin patches to facilitate immune cell migration in dense tissues. <i>Developmental
    Cell</i>. 2022;57(1):47-62.e9. doi:<a href="https://doi.org/10.1016/j.devcel.2021.11.024">10.1016/j.devcel.2021.11.024</a>
  apa: Gaertner, F., Dos Reis Rodrigues, P., de Vries, I., Hons, M., Aguilera, J.,
    Riedl, M., … Sixt, M. K. (2022). WASp triggers mechanosensitive actin patches
    to facilitate immune cell migration in dense tissues. <i>Developmental Cell</i>.
    Cell Press. <a href="https://doi.org/10.1016/j.devcel.2021.11.024">https://doi.org/10.1016/j.devcel.2021.11.024</a>
  chicago: Gaertner, Florian, Patricia Dos Reis Rodrigues, Ingrid de Vries, Miroslav
    Hons, Juan Aguilera, Michael Riedl, Alexander F Leithner, et al. “WASp Triggers
    Mechanosensitive Actin Patches to Facilitate Immune Cell Migration in Dense Tissues.”
    <i>Developmental Cell</i>. Cell Press, 2022. <a href="https://doi.org/10.1016/j.devcel.2021.11.024">https://doi.org/10.1016/j.devcel.2021.11.024</a>.
  ieee: F. Gaertner <i>et al.</i>, “WASp triggers mechanosensitive actin patches to
    facilitate immune cell migration in dense tissues,” <i>Developmental Cell</i>,
    vol. 57, no. 1. Cell Press, p. 47–62.e9, 2022.
  ista: Gaertner F, Dos Reis Rodrigues P, de Vries I, Hons M, Aguilera J, Riedl M,
    Leithner AF, Tasciyan S, Kopf A, Merrin J, Zheden V, Kaufmann W, Hauschild R,
    Sixt MK. 2022. WASp triggers mechanosensitive actin patches to facilitate immune
    cell migration in dense tissues. Developmental Cell. 57(1), 47–62.e9.
  mla: Gaertner, Florian, et al. “WASp Triggers Mechanosensitive Actin Patches to
    Facilitate Immune Cell Migration in Dense Tissues.” <i>Developmental Cell</i>,
    vol. 57, no. 1, Cell Press, 2022, p. 47–62.e9, doi:<a href="https://doi.org/10.1016/j.devcel.2021.11.024">10.1016/j.devcel.2021.11.024</a>.
  short: F. Gaertner, P. Dos Reis Rodrigues, I. de Vries, M. Hons, J. Aguilera, M.
    Riedl, A.F. Leithner, S. Tasciyan, A. Kopf, J. Merrin, V. Zheden, W. Kaufmann,
    R. Hauschild, M.K. Sixt, Developmental Cell 57 (2022) 47–62.e9.
corr_author: '1'
date_created: 2022-01-30T23:01:33Z
date_published: 2022-01-10T00:00:00Z
date_updated: 2026-06-21T22:31:15Z
day: '10'
ddc:
- '570'
department:
- _id: MiSi
- _id: EM-Fac
- _id: NanoFab
- _id: BjHo
doi: 10.1016/j.devcel.2021.11.024
ec_funded: 1
external_id:
  isi:
  - '000768933800005'
  pmid:
  - '34919802'
intvolume: '        57'
isi: 1
issue: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
main_file_link:
- open_access: '1'
  url: https://www.sciencedirect.com/science/article/pii/S1534580721009497
month: '01'
oa: 1
oa_version: Published Version
page: 47-62.e9
pmid: 1
project:
- _id: 260AA4E2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '747687'
  name: Mechanical Adaptation of Lamellipodial Actin Networks in Migrating Cells
- _id: 25FE9508-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '724373'
  name: Cellular Navigation Along Spatial Gradients
publication: Developmental Cell
publication_identifier:
  eissn:
  - 1878-1551
  issn:
  - 1534-5807
publication_status: published
publisher: Cell Press
quality_controlled: '1'
related_material:
  record:
  - id: '20149'
    relation: dissertation_contains
    status: public
  - id: '12726'
    relation: dissertation_contains
    status: public
  - id: '14530'
    relation: dissertation_contains
    status: public
  - id: '12401'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: WASp triggers mechanosensitive actin patches to facilitate immune cell migration
  in dense tissues
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 57
year: '2022'
...
---
_id: '11498'
abstract:
- lang: eng
  text: Rest-frame ultraviolet (UV) emission lines probe electron densities, gas-phase
    abundances, metallicities, and ionization parameters of the emitting star-forming
    galaxies and their environments. The strongest main UV emission line, Lyα, has
    been instrumental in advancing the general knowledge of galaxy formation in the
    early universe. However, observing Lyα emission becomes increasingly challenging
    at z ≳ 6 when the neutral hydrogen fraction of the circumgalactic and intergalactic
    media increases. Secondary weaker UV emission lines provide important alternative
    methods for studying galaxy properties at high redshift. We present a large sample
    of rest-frame UV emission line sources at intermediate redshift for calibrating
    and exploring the connection between secondary UV lines and the emitting galaxies’
    physical properties and their Lyα emission. The sample of 2052 emission line sources
    with 1.5 < z < 6.4 was collected from integral field data from the MUSE-Wide and
    MUSE-Deep surveys taken as part of Guaranteed Time Observations. The objects were
    selected through untargeted source detection (i.e., no preselection of sources
    as in dedicated spectroscopic campaigns) in the three-dimensional MUSE data cubes.
    We searched optimally extracted one-dimensional spectra of the full sample for
    UV emission features via emission line template matching, resulting in a sample
    of more than 100 rest-frame UV emission line detections. We show that the detection
    efficiency of (non-Lyα) UV emission lines increases with survey depth, and that
    the emission line strength of He IIλ1640 Å, [O III] λ1661 + O III] λ1666, and
    [Si III] λ1883 + Si III] λ1892 correlate with the strength of [C III] λ1907 +
    C III] λ1909. The rest-frame equivalent width (EW0) of [C III] λ1907 + C III]
    λ1909 is found to be roughly 0.22 ± 0.18 of EW0(Lyα). We measured the velocity
    offsets of resonant emission lines with respect to systemic tracers. For C IVλ1548
    + C IVλ1551 we find that ΔvC IV ≲ 250 km s−1, whereas ΔvLyα falls in the range
    of 250−500 km s−1 which is in agreement with previous results from the literature.
    The electron density ne measured from [Si III] λ1883 + Si III] λ1892 and [C III]
    λ1907 + C III] λ1909 line flux ratios is generally < 105 cm−3 and the gas-phase
    abundance is below solar at 12 + log10(O/H)≈8. Lastly, we used “PhotoIonization
    Model Probability Density Functions” to infer physical parameters of the full
    sample and individual systems based on photoionization model parameter grids and
    observational constraints from our UV emission line searches. This reveals that
    the UV line emitters generally have ionization parameter log10(U) ≈ −2.5 and metal
    mass fractions that scatter around Z ≈ 10−2, that is Z ≈ 0.66 Z⊙. Value-added
    catalogs of the full sample of MUSE objects studied in this work and a collection
    of UV line emitters from the literature are provided with this paper.
acknowledgement: 'We would like to thank Charlotte Mason for useful discussions and
  for providing the data for the curves shown in Fig. 13 and Dawn Erb for providing
  the observational data for the comparison sample studied by Steidel et al. (2014),
  also shown in Fig. 13. This work has been supported by the BMBF grant 05A14BAC and
  we acknowledge support by the Competitive Fund of the Leibniz Association through
  grant SAW-2015-AIP-2. AF acknowledges the support from grant PRIN MIUR2017-20173ML3WW_001.
  JS acknowledges the support from Vici grant 639.043.409 from the Dutch Research
  Council (NWO). GM received funding from the European Union’s Horizon 2020 research
  and innovation programme under the Marie Sklodowska-Curie grant agreement No MARACAS
  – DLV-896778. This paper is based on observations collected at the European Organisation
  for Astronomical Research in the Southern Hemisphere under ESO programmes 094.A-0289(B),
  095.A-0010(A), 096.A-0045(A), 096.A-0045(B), 094.A-0205, 095.A-0240, 096.A-0090,
  097.A-0160, and 098.A-0017. This paper also makes use of observations made with
  the NASA/ESA Hubble Space Telescope obtained at STScI. This research made use of
  the following programs and open-source packages for Python and we are thankful to
  their developers: DS9 (Joye & Mandel 2003), Astropy (Astropy Collaboration 2013,
  2018), APLpy (Robitaille & Bressert 2012), iPython (Pérez & Granger 2007), numpy
  (van der Walt et al. 2011), matplotlib (Hunter 2007), and SciPy (Jones et al. 2001).'
article_number: A80
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: K. B.
  full_name: Schmidt, K. B.
  last_name: Schmidt
- first_name: J.
  full_name: Kerutt, J.
  last_name: Kerutt
- first_name: L.
  full_name: Wisotzki, L.
  last_name: Wisotzki
- first_name: T.
  full_name: Urrutia, T.
  last_name: Urrutia
- first_name: A.
  full_name: Feltre, A.
  last_name: Feltre
- first_name: M. V.
  full_name: Maseda, M. V.
  last_name: Maseda
- first_name: T.
  full_name: Nanayakkara, T.
  last_name: Nanayakkara
- first_name: R.
  full_name: Bacon, R.
  last_name: Bacon
- first_name: L. A.
  full_name: Boogaard, L. A.
  last_name: Boogaard
- first_name: S.
  full_name: Conseil, S.
  last_name: Conseil
- first_name: T.
  full_name: Contini, T.
  last_name: Contini
- first_name: E. C.
  full_name: Herenz, E. C.
  last_name: Herenz
- first_name: W.
  full_name: Kollatschny, W.
  last_name: Kollatschny
- first_name: M.
  full_name: Krumpe, M.
  last_name: Krumpe
- first_name: F.
  full_name: Leclercq, F.
  last_name: Leclercq
- first_name: G.
  full_name: Mahler, G.
  last_name: Mahler
- first_name: Jorryt J
  full_name: Matthee, Jorryt J
  id: 7439a258-f3c0-11ec-9501-9df22fe06720
  last_name: Matthee
  orcid: 0000-0003-2871-127X
- first_name: V.
  full_name: Mauerhofer, V.
  last_name: Mauerhofer
- first_name: J.
  full_name: Richard, J.
  last_name: Richard
- first_name: J.
  full_name: Schaye, J.
  last_name: Schaye
citation:
  ama: Schmidt KB, Kerutt J, Wisotzki L, et al. Recovery and analysis of rest-frame
    UV emission lines in 2052 galaxies observed with MUSE at 1.5 &#60; z &#60; 6.4.
    <i>Astronomy &#38; Astrophysics</i>. 2021;654. doi:<a href="https://doi.org/10.1051/0004-6361/202140876">10.1051/0004-6361/202140876</a>
  apa: Schmidt, K. B., Kerutt, J., Wisotzki, L., Urrutia, T., Feltre, A., Maseda,
    M. V., … Schaye, J. (2021). Recovery and analysis of rest-frame UV emission lines
    in 2052 galaxies observed with MUSE at 1.5 &#60; z &#60; 6.4. <i>Astronomy &#38;
    Astrophysics</i>. EDP Sciences. <a href="https://doi.org/10.1051/0004-6361/202140876">https://doi.org/10.1051/0004-6361/202140876</a>
  chicago: Schmidt, K. B., J. Kerutt, L. Wisotzki, T. Urrutia, A. Feltre, M. V. Maseda,
    T. Nanayakkara, et al. “Recovery and Analysis of Rest-Frame UV Emission Lines
    in 2052 Galaxies Observed with MUSE at 1.5 &#60; z &#60; 6.4.” <i>Astronomy &#38;
    Astrophysics</i>. EDP Sciences, 2021. <a href="https://doi.org/10.1051/0004-6361/202140876">https://doi.org/10.1051/0004-6361/202140876</a>.
  ieee: K. B. Schmidt <i>et al.</i>, “Recovery and analysis of rest-frame UV emission
    lines in 2052 galaxies observed with MUSE at 1.5 &#60; z &#60; 6.4,” <i>Astronomy
    &#38; Astrophysics</i>, vol. 654. EDP Sciences, 2021.
  ista: Schmidt KB, Kerutt J, Wisotzki L, Urrutia T, Feltre A, Maseda MV, Nanayakkara
    T, Bacon R, Boogaard LA, Conseil S, Contini T, Herenz EC, Kollatschny W, Krumpe
    M, Leclercq F, Mahler G, Matthee JJ, Mauerhofer V, Richard J, Schaye J. 2021.
    Recovery and analysis of rest-frame UV emission lines in 2052 galaxies observed
    with MUSE at 1.5 &#60; z &#60; 6.4. Astronomy &#38; Astrophysics. 654, A80.
  mla: Schmidt, K. B., et al. “Recovery and Analysis of Rest-Frame UV Emission Lines
    in 2052 Galaxies Observed with MUSE at 1.5 &#60; z &#60; 6.4.” <i>Astronomy &#38;
    Astrophysics</i>, vol. 654, A80, EDP Sciences, 2021, doi:<a href="https://doi.org/10.1051/0004-6361/202140876">10.1051/0004-6361/202140876</a>.
  short: K.B. Schmidt, J. Kerutt, L. Wisotzki, T. Urrutia, A. Feltre, M.V. Maseda,
    T. Nanayakkara, R. Bacon, L.A. Boogaard, S. Conseil, T. Contini, E.C. Herenz,
    W. Kollatschny, M. Krumpe, F. Leclercq, G. Mahler, J.J. Matthee, V. Mauerhofer,
    J. Richard, J. Schaye, Astronomy &#38; Astrophysics 654 (2021).
date_created: 2022-07-06T08:49:03Z
date_published: 2021-10-15T00:00:00Z
date_updated: 2022-07-19T09:34:36Z
day: '15'
doi: 10.1051/0004-6361/202140876
extern: '1'
external_id:
  arxiv:
  - '2108.01713'
intvolume: '       654'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'ultraviolet: galaxies / galaxies: high-redshift / galaxies: ISM / ISM: lines and
  bands / methods: observational / techniques: imaging spectroscopy'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/2108.01713
month: '10'
oa: 1
oa_version: Published Version
publication: Astronomy & Astrophysics
publication_identifier:
  eissn:
  - 1432-0746
  issn:
  - 0004-6361
publication_status: published
publisher: EDP Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Recovery and analysis of rest-frame UV emission lines in 2052 galaxies observed
  with MUSE at 1.5 < z < 6.4
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 654
year: '2021'
...
