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Walsh, S. L.

Publications and source records attributed to Walsh, S. L..

3 recordsLinked to original sources

Innate building blocks underly socially learned call sequences

Recent evidence of extensive call sequence use in non-human primates has led to the theory that syntax evolved to mitigate the constraints of their genetically fixed repertoires, before vocal production learning later emerged in humans. However, evidence of similarly extensive sequence repertoires in an open-ended vocal production learner--the Western Australian magpie (Gymnorhinatibicendorsalis)--offers a unique opportunity to explore potential alternative pathways to syntactic communication. Our previous work revealed fledgling magpies learn group-specific repertoires of structured call sequences from their social contacts, with more sociable individuals acquiring larger repertoires earlier in development. Notably however, the individual vocal segments that combine to form their calls and call sequences were shared across groups and emerged as early as the first week post-fledging--suggesting the underlying vocal elements may not be learned. Here we utilised acoustic neighbourhood-based dimensionality reduction to compare clustering patterns of vocal segments across magpie fledgling developmental stages, and between fledglings and adults. We found no evidence of acoustic development over time, and no significant distinction between fledgling and adult productions of the same vocal segments. The same coarticulatory effects--where a vocal element is produced differently when combined with another--and geographic variation established previously in adults were supported in fledglings too. These findings support that the vocal building blocks underpinning magpie call sequences are innate, suggesting usage learning better explains how fledglings learn to combine calls. In a species capable of open-ended production learning, this suggests learning to combine existing signals may be more adaptive than productively learning new ones. Rather than evolving solely to compensate for genetically fixed repertoires, syntax may have evolved as a flexible, convergent solution to the various challenges of expanding communicative capacity--whether due to genetic constraints, cognitive limitations or the cost of establishing new meaning in novel signals.

animal behavior and cognition↗

Socially learned call sequences reveal gradual development of higher-order structure

Syntax was long considered to distinguish human language from other vocal systems, with parallels in non-human animals historically limited to song. However, song lacks discrete meaning, which is a crucial pre-requisite of linguistic syntax. Over the last two decades evidence of combinatoriality in the discrete, semantic calls of an array of taxa has accumulated, providing the opportunity to investigate potentially closer parallels to language. However, most examples remain limited to small repertoires of simple two-call sequences, preventing evidence of complex internal structuring like that seen in human sentences. The recent discovery that several species produce extensive repertoires of much longer call sequences, has provided the opportunity to investigate the full extent of syntactic structure in non-human call systems. Here we demonstrate that Western Australian magpies (Gymnorhina tibicen dorsalis) use multi-level structured ordering rules within their semantic call sequences and that these ordering rules are learned during development. Specifically, we find that calls within sequences up to 15 calls long depend on the two calls given prior and that independently produced segments ( phonemes), calls, and sequences recombine into longer structures, indicating hierarchical organisation. This represents the first evidence of multi-level non-adjacent organisation and learned syntactic structure in a semantic non-human system.

animal behavior and cognition↗

Molecular tracking devices quantify antigen distribution and archiving in the lymph node

Live, attenuated vaccines generate humoral and cellular immune memory, increasing the duration of protective immune memory. We previously found that antigens derived from vaccination or viral infection persist within lymphatic endothelial cells (LECs) beyond the clearance of the infection, a process we termed "antigen archiving". Technical limitations of fluorescent labeling have precluded a complete picture of antigen archiving across cell types in the lymph node. We developed a "molecular tracking device" to follow the distribution, acquisition, and retention of antigen in the lymph node. We immunized mice with an antigen conjugated to a nuclease-resistant DNA tag and used single-cell mRNA sequencing to quantify its abundance in lymph node hematopoietic and non-hematopoietic cell types. At early and late time points after vaccination we found antigen acquisition by dendritic cell populations (DCs), associated expression of genes involved in DC activation and antigen processing, and antigen acquisition and archiving by LECs as well as unexpected stromal cell types. Variable antigen levels in LECs enabled the identification of caveolar endocytosis as a mechanism of antigen acquisition or retention. Molecular tracking devices enable new approaches to study dynamic tissue dissemination of antigens and identify new mechanisms of antigen acquisition and retention at cellular resolution in vivo.

immunology↗