Alexandra Kerbl

Dr. Alexandra Kerbl

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Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 November 2020 in Nature Ecology & Evolution
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JMJosé M. Martín-Durán
José M. Martín-Durán
BVBruno C. Vellutini
Bruno C. Vellutini
FMFerdinand Marlétaz
Ferdinand Marlétaz
VCViviana Cetrangolo
Viviana Cetrangolo
NCNevena Cvetesic
Nevena Cvetesic
AHAndreas Hejnol
Andreas Hejnol
The causes and consequences of genome reduction in animals are unclear because our understanding of this process mostly relies on lineages with often exceptionally high rates of evolution. Here, we decode the compact 73.8-megabase genome ofDimorphilus gyrociliatus, a meiobenthic segmented worm. TheD. gyrociliatusgenome retains traits classically associated with larger and slower-evolving genomes, such as an ordered, intact Hox cluster, a generally conserved developmental toolkit and traces of ancestral bilaterian linkage. Unlike some other animals with small genomes, the analysis of theD. gyrociliatusepigenome revealed canonical features of genome regulation, excluding the presence of operons andtrans-splicing. Instead, the gene-denseD. gyrociliatusgenome presents a divergent Myc pathway, a key physiological regulator of growth, proliferation and genome stability in animals. Altogether, our results uncover a conservative route to genome compaction in annelids, reminiscent of that observed in the vertebrateTakifugu rubripes.

12 February 2021 in Diversity
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Katrine WorsaaeKatrine Worsaae
Katrine Worsaae
AKAlexandra Kerbl
Alexandra Kerbl
MDMAIKON DI DOMENICO
MAIKON DI DOMENICO
Brett C. GonzalezBrett C. Gonzalez
Brett C. Gonzalez
Nicolas Tarik BekkoucheNicolas Tarik Bekkouche
Nicolas Tarik Bekkouche
Alejandro MartínezAlejandro Martínez
Alejandro Martínez
Members of the following marine annelid families are found almost exclusively in the interstitial environment and are highly adapted to move between sand grains, relying mostly on ciliary locomotion: Apharyngtidae n. fam., Dinophilidae, Diurodrilidae, Nerillidae, Lobatocerebridae, Parergodrilidae, Polygordiidae, Protodrilidae, Protodriloididae, Psammodrilidae and Saccocirridae. This article provides a review of the evolution, systematics, and diversity of these families, with the exception of Parergodrilidae, which was detailed in the review of Orbiniida by Meca, Zhadan, and Struck within this Special Issue. While several of the discussed families have previously only been known by a few described species, recent surveys inclusive of molecular approaches have increased the number of species, showing that all of the aforementioned families exhibit a high degree of cryptic diversity shadowed by a limited number of recognizable morphological traits. This is a challenge for studies of the evolution, taxonomy, and diversity of interstitial families as well as for their identification and incorporation into ecological surveys. By compiling a comprehensive and updated review on these interstitial families, we hope to promote new studies on their intriguing evolutionary histories, adapted life forms and high and hidden diversity.

17 March 2025 in Communications Biology
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Alejandro MartínezAlejandro Martínez
Alejandro Martínez
SBStefano Bonaglia
Stefano Bonaglia
MDMAIKON DI DOMENICO
MAIKON DI DOMENICO
GFGustavo Fonseca
Gustavo Fonseca
JIJeroen Ingels
Jeroen Ingels
Diego FontanetoDiego Fontaneto
Diego Fontaneto
This paper identifies the top-50 priority questions for meiofaunal research, highlighting their critical roles in biogeochemical cycles and biodiversity. It calls for a balanced research agenda, international cooperation, and advances in technology to overcome current challenges and unlock meiofauna’s full potential. This paper identifies the top-50 priority questions for meiofaunal research, highlighting their critical roles in biogeochemical cycles and biodiversity. It calls for a balanced research agenda, international cooperation, and advances in technology to overcome current challenges and unlock meiofauna’s full potential.

8 November 2016 in Frontiers in Zoology
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AKAlexandra Kerbl
Alexandra Kerbl
EFElizaveta Fofanova
Elizaveta Fofanova
TMTatiana D Mayorova
Tatiana D Mayorova
EVElena E. Voronezhskaya
Elena E. Voronezhskaya
Katrine WorsaaeKatrine Worsaae
Katrine Worsaae
Several independent meiofaunal lineages are suggested to have originated through progenesis, however, morphological support for this heterochronous process is still lacking. Progenesis is defined as an arrest of somatic development (synchronously in various organ systems) due to early maturation, resulting in adults resembling larvae or juveniles of the ancestors. Accordingly, we established a detailed neuromuscular developmental atlas of two closely related Dinophilidae using immunohistochemistry and CLSM. This allows us to test for progenesis, questioning whether i) the adult smaller, dimorphic Dinophilus gyrociliatus resembles a younger developmental stage of the larger, monomorphic D. taeniatus and whether ii) dwarf males of D. gyrociliatus resemble an early developmental stage of D. gyrociliatus females. Both species form longitudinal muscle bundles first, followed by circular muscles, creating a grid of body wall musculature, which is the densest in adult D. taeniatus, while the architecture in adult female D. gyrociliatus resembles that of prehatching D. taeniatus. Both species display a subepidermal ganglionated nervous system with an anterior dorsal brain and five longitudinal ventral nerve bundles with six sets of segmental commissures (associated with paired ganglia). Neural differentiation of D. taeniatus and female D. gyrociliatus commissures occurs before hatching: both species start out forming one transverse neurite bundle per segment, which are thereafter joined by additional thin bundles. Whereas D. gyrociliatus arrests its development at this stage, adult D. taeniatus condenses the thin commissures again into one thick commissural bundle per segment. Generally, D. taeniatus adults demonstrate a seemingly more organized (= segmental) pattern of serotonin-like and FMRFamide-like immunoreactive elements. The dwarf male of D. gyrociliatus displays a highly aberrant neuromuscular system, showing no close resemblance to any early developmental stage of female Dinophilus, although the onset of muscular development mirrors the early myogenesis in females. The apparent synchronous arrest of nervous and muscular development in adult female D. gyrociliatus, resembling the prehatching stage of D. taeniatus, suggests that D. gyrociliatus have originated through progenesis. The synchrony in arrest of three organ systems, which show opposing reduction and addition of elements, presents one of the morphologically best-argued cases of progenesis within Spiralia.

1 September 2013 in Journal of Experimental Marine Biology and Ecology
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AKAlexandra Kerbl
Alexandra Kerbl
SHStephan Handschuh
Stephan Handschuh
MNMarie-Therese Nödl
Marie-Therese Nödl
BMBrian D. Metscher
Brian D. Metscher
MWManfred Walzl
Manfred Walzl
AWAndreas Wanninger
Andreas Wanninger

10 December 2015 in BMC Ecology and Evolution
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AKAlexandra Kerbl
Alexandra Kerbl
NBNicolas Bekkouche
Nicolas Bekkouche
WSWolfgang Sterrer
Wolfgang Sterrer
Katrine WorsaaeKatrine Worsaae
Katrine Worsaae
Background: The microscopic worm group Lobatocerebridae has been regarded a ‘problematicum’, with the systematic relationship being highly debated until a recent phylogenomic study placed them within annelids (Curr Biol 25: 2000-2006, 2015). To date, a morphological comparison with other spiralian taxa lacks detailed information on the nervous and muscular system, which is here presented forLobatocerebrum riegerin. sp. based on immunohistochemistry and confocal laser scanning microscopy, supported by TEM and live observations.Results: The musculature is organized as a grid of longitudinal muscles and transverse muscular ring complexes in the trunk. The rostrum is supplied by longitudinal muscles and only a few transverse muscles. The intraepidermal central nervous system consists of a big, multi-lobed brain, nine major nerve bundles extending anteriorly into the rostrum and two lateral and one median cord extending posteriorly to the anus, connected by five commissures. The glandular epidermis has at least three types of mucus secreting glands and one type of adhesive unicellular glands.Conclusions: No exclusive “annelid characters” could be found in the neuromuscular system of Lobatocerebridae, except for perhaps the mid-ventral nerve. However, none of the observed structures disputes its position within this group. The neuromuscular and glandular system ofL. riegerin. sp. shows similarities to those of meiofaunal annelids such as Dinophilidae and Protodrilidae, yet likewise to Gnathostomulida and catenulid Platyhelminthes, all living in the restrictive interstitial environment among sand grains. It therefore suggests an extreme evolutionary plasticity of annelid nervous and muscular architecture, previously regarded as highly conservative organ systems throughout metazoan evolution.