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  <doc>
    <id>65059</id>
    <completedYear/>
    <publishedYear>2025</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume/>
    <type>poster</type>
    <publisherName/>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
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    <title language="eng">Multivalent Myteries: How Termite  Chromosome Chains Shape Evolution</title>
    <abstract language="eng">Termites challenge long-standing assumptions about insect social&#13;
evolution. One important difference compared to the social ants, bees&#13;
and wasps lies in their chromosomes: termites are diploid, with X/Y sex&#13;
differentiation observed in most species and males playing active roles&#13;
across all castes and life stages. Adding to their uniqueness, termites&#13;
exhibit multivalent chromosome chains during male meiosis—an&#13;
intriguing and seldom seen feature of eukaryote evolution. These chains,&#13;
in addition to other chromosomal formations, such as bivalent rings and&#13;
rods, may serve to suppress recombination, thereby mitigating against&#13;
the potentially harmful effects of inbreeding. Again, this positions&#13;
termites as an important contrasting study system to other social insect&#13;
groups, where recombination rates tend to be elevated. Multivalent&#13;
chromosome chains may also play a significant role in speciation&#13;
processes by increasing the likelihood of chromosomal translocations and&#13;
promoting genomic islands of divergence. In European Reticulitermes,&#13;
variability in chain length and stability both between and within species&#13;
provides a compelling model system for studying the evolutionary&#13;
importance of multivalent chromosome chains at intra- and interspecific&#13;
levels and at different evolutionary time scales. To investigate these&#13;
dynamics, we collected over 200 colonies of Reticulitermes species across&#13;
the Mediterranean, generating de novo reference genomes,&#13;
comprehensive population genomic as well as karyotypic data from three&#13;
recently diverged species. Our findings shed light on the intricate&#13;
relationship between chromosomal architecture and evolutionary&#13;
mechanisms in termites, offering new insight into how genome structure&#13;
shapes species evolution.</abstract>
    <enrichment key="eventName">ESEB 2025 Congress</enrichment>
    <enrichment key="eventPlace">Barcelona, Spain</enrichment>
    <enrichment key="eventStart">17.08.2025</enrichment>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="opus.doi.autoCreate">false</enrichment>
    <enrichment key="opus.urn.autoCreate">true</enrichment>
    <author>Mara Jean Julseth</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Termites</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Chromosome evolution</value>
    </subject>
    <collection role="ddc" number="628">Sanitär- und Kommunaltechnik; Umwelttechnik</collection>
    <collection role="institutes" number="">4 Material und Umwelt</collection>
    <collection role="themenfelder" number="">Umwelt</collection>
    <collection role="themenfelder" number="">Umwelt-Material-Interaktionen</collection>
    <collection role="fulltextaccess" number="">Datei im Netzwerk der BAM verfügbar ("Closed Access")</collection>
    <collection role="literaturgattung" number="">Präsentation</collection>
    <collection role="institutes" number="">4.3 Molekulare und angewandte Entomologie</collection>
  </doc>
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