Biology subjects

Strausfeld, N. J.

Publications and source records attributed to Strausfeld, N. J..

6 recordsLinked to original sources

bioRxiv2026

Cambrian Artiopoda Reveals a Constraint in Euarthropod Brain Evolution

Cambrian stem mandibulates and chelicerates have provided robust evidence of brains that conform to a cerebral ground pattern also defining extant euarthopods. But information about the brains of trilobites or their immediate relatives remains a mystery. Here we describe the detailed organization of the specialized brain of Xandarella spectaculum, a member of the subphylum Trilobitomorpha which went extinct at the end Permian. While retaining the pre-Cambrian cephalic ground pattern as three seriate domains, empirical evidence indicates clade-specific accentuation of some and loss of other neural arrangements typifying extant mandibulates. The trilobitomorph deutocerebral organization is dominated by exaggerated glomerular centers whereas its prominent lateral eyes supply minute visual centers. Paired ocelli are associated with the prominent prosocerebral bridge of the forebrain, an essential center for path integration. Together these modifications indicate neural organization typifying some extant benthic crustaceans and even hexapods that engage in foraging behaviors. With reference to existing neurological attributes of living pancrustaceans major divergences of the trilobitomorph brain from the ancestral cerebral ground pattern may have weakened its resilience to geo-ecological disruptions and hence the final extinction of the clade to which trilobitomorphs belong.

evolutionary biology↗

bioRxiv2025

A pancrustacean brain and its visual systems define a Cambrian great appendage arthropod.

Early Cambrian fossils from the Chengjiang biota demonstrate that over half a billion years ago early stem euarthropods existed coevally with representatives of already recognizable crown groups. Prominent stem taxa were Fuxianhuia protensa and Alalcomenaeus whose cerebral and ganglionic traits identify them as, respectively, stem mandibulates and stem chelicerates. Here we report features of the visual systems and brain of the enigmatic lower Cambrian stem euarthropod Jianfengia multisegmentalis, which despite the absence of trunk tagmatization reveals neural traits that justify its inclusion within stem Pancrustacea also known as Tetraconata. The sutured eyestalks of Jianfengia, typifying crown Malacostraca, terminate as compound eyes populated by ommatidia that reveal tetradic structures indicative of cone-building Semper cells. Preserved neuropils and tracts in the eyestalks of Jianfengia resolve nested optic neuropils as occur in eucrustaceans. The nauplius-like eyes of Jianfengia and their associated nerves supply a discrete forebrain region, as they do in pancrustaceans. These attributes distinguish Pancrustacea from stem Chelicerata and extant Myriapoda as does the organization of the jianfengiid deutocerebrum and tritocerebrum. In the absence of external traits that differentiate identities amongst stem euarthropods, neuroanatomical traits provide a powerful tool for discerning characteristic distinctions and correspondences for elucidating euarthropod relationships. Here, we demonstrate that cerebral arrangements in Jianfengia correspond to those of pancrustaceans existing today.

evolutionary biology↗

bioRxiv2024

Marine Origin of the Arachnid Brain Reveals Early Divergence of Chelicerata

Fossils from the lower Cambrian provide crucial insights into the diversification of arthropod lineages: Mandibulata, exemplified by centipedes, insects, and crustaceans; and Chelicerata, represented by sea spiders, horseshoe crabs, and arachnids, the last including spiders, scorpions, and ticks1. Two mid-Cambrian genera claimed as stem chelicerates are Mollisonia and Sanctacaris, defined by a carapaced prosoma equipped with clustered limbs, followed by a segmented trunk opisthosoma equipped with appendages for swimming and respiration2-4. Up to the present, the phyletic status of Mollisoniidae and Sanctacariidae has been that of a basal chelicerate2, stemward of Leanchoiliidae, whose neuromorphology resembles that of extant Merostomata (horseshoe crabs)5. Here, we identify preserved traces of neuronal tissues in Mollisonia symmetrica that crucially depart from a merostome organization. Instead, a radiating organization of metameric neuropils occupying most of its prosoma is situated behind a pair of oval unsegmented neuropils directly connected to paired chelicerae extending from the front of the prosoma. The disposition and connections of these neuropils is the neuroanatomical signature that denotes a complete reversal of the three genetically distinct domains defining arthropod brains6. Thus, in Mollisonia the deutocerebrum is the most rostral domain with the proso-and protocerebral domains folded backwards such that tracts from the principal eyes extend caudally to reach their prosocerebral destination. These defining neuromorphological features illuminate a marine origin of Arachnida from which evolved the planets most successful arthropodan predators.

paleontology↗

bioRxiv2019

Mushroom Body Homology and Divergence across Pancrustacea

Descriptions of crustacean brains have mainly focused on three highly derived lineages: the reptantian infraorders represented by spiny lobsters, lobsters, and crayfish. Those descriptions advocate the view that dome- or cap-like neuropils, referred to as "hemiellipsoid bodies," are the ground pattern organization of centers that are comparable to insect mushroom bodies in processing olfactory information. Here we challenge the doctrine that hemiellipsoid bodies are a derived trait of crustaceans, whereas mushroom bodies are a derived trait of hexapods. We demonstrate that mushroom bodies typify lineages that arose before Reptantia and exist in Reptantia. We show that evolved variations of the mushroom body ground pattern are, in some lineages, defined by extreme diminution or loss and, in others, by the incorporation of mushroom body circuits into lobeless centers. Such transformations are ascribed to modifications of the columnar organization of mushroom body lobes that, as shown in Drosophila and other hexapods, contain networks essential for learning and memory. We propose that lobed mushroom bodies distinguish crustaceans that negotiate the multidimensionality of complex ecologies, where continuous updating of multistimulus valence and memory is paramount.

neuroscience↗

bioRxiv2019

Ancestral regulatory mechanisms specify conserved midbrain circuitry in arthropods and vertebrates

Corresponding attributes of neural development and function suggest arthropod and vertebrate brains may have an evolutionarily conserved organization. However, the underlying mechanisms have remained elusive. Here we identify a gene regulatory and character identity network defining the deutocerebral-tritocerebral boundary (DTB) in Drosophila. We show this network comprises genes homologous to those directing midbrain-hindbrain boundary (MHB) formation in vertebrates and their closest chordate relatives. Genetic tracing reveals that the embryonic DTB gives rise to adult midbrain circuits that in flies control auditory and vestibular information processing and motor coordination, as do MHB-derived circuits in vertebrates. DTB-specific gene expression and function is directed by cis-regulatory elements (CREs) of developmental control genes that include homologs of mammalian Zinc finger of the cerebellum and Purkinje cell protein 4. Moreover, Drosophila DTB-specific CREs correspond to regulatory sequences of human ENGRAILED-2, PAX-2 and DACHSHUND-1 that direct MHB-specific expression in the embryonic mouse brain. Together, these findings imply ancestral regulatory mechanisms mediating the genetic specification of midbrain-cerebellar circuitry for balance and motor control that may predated the radiation of cephalic nervous systems across the animal kingdom.

neuroscience↗

bioRxiv2017

A lineage-related reciprocal inhibition circuitry for sensory-motor action selection

The insect central complex and vertebrate basal ganglia are forebrain centres involved in selection and maintenance of behavioural actions. However, little is known about the formation of the underlying circuits, or how they integrate sensory information for motor actions. Here, we show that paired embryonic neuroblasts generate central complex ring neurons that mediate sensory-motor transformation and action selection in Drosophila. Lineage analysis resolves four ring neuron subtypes, R1-R4, that form GABAergic inhibition circuitry among inhibitory sister cells. Genetic manipulations, together with functional imaging, demonstrate subtype-specific R neurons mediate the selection and maintenance of behavioural activity. A computational model substantiates genetic and behavioural observations suggesting that R neuron circuitry functions as salience detector using competitive inhibition to amplify, maintain or switch between activity states. The resultant gating mechanism translates facilitation, inhibition and disinhibition of behavioural activity as R neuron functions into selection of motor actions and their organisation into action sequences.

neuroscience↗