A record of fossil shallow-water whale falls from Italy

Twenty-five Neogene-Quaternary whales hosted in Italian museum collections and their associated fauna were analysed for evidence of whale-fall community development in shallow-water settings. The degree of bone articulation, completeness of the skeleton and lithology of the embedding sediments were used to gather information on relative water depth, water energy, sedimentation rate and overall environmental predictability around the bones. Shark teeth and hard-shelled invertebrates with a necrophagous diet in close association with the bones were used as evidence of scavenging. Fossil bone bioerosion, microbially mediated cementation and other mollusc shells in the proximity of the remains informed on past biological activity around the bones. The results are consistent with the hypothesis that shallow-water whale falls differ from their deep-water counterparts. Taphonomic pathways are more variable on the shelf and whale carcasses may not go through all steps of the ecological succession as recognised in the deep sea. Whilst the mobile scavenger and the enrichment opportunistic stages are well represented, chemosynthetic taxa typical of the sulphophilic stage were recovered only in one instance. The presence of a generalist fauna among the suspension feeding bivalves and carnivorous gastropods, and the extreme rarity of chemosynthetic taxa, suggest that predatory pressure rules out whale-fall specialists from shallow shelf settings as in analogous cold seep and vent shallow-water communities. © 2014 The Lethaia Foundation

Variable levels of drift in tunicate cardiopharyngeal gene regulatory elements.

Background: Mutations in gene regulatory networks often lead to genetic divergence without impacting gene expression or developmental patterning. The rules governing this process of developmental systems drift, including the variable impact of selective constraints on different nodes in a gene regulatory network, remain poorly delineated. Results: Here we examine developmental systems drift within the cardiopharyngeal gene regulatory networks of two tunicate species, Corella inflata and Ciona robusta. Cross-species analysis of regulatory elements suggests that trans-regulatory architecture is largely conserved between these highly divergent species. In contrast, cis-regulatory elements within this network exhibit distinct levels of conservation. In particular, while most of the regulatory elements we analyzed showed extensive rearrangements of functional binding sites, the enhancer for the cardiopharyngeal transcription factor FoxF is remarkably well-conserved. Even minor alterations in spacing between binding sites lead to loss of FoxF enhancer function, suggesting that bound trans-factors form position-dependent complexes. Conclusions: Our findings reveal heterogeneous levels of divergence across cardiopharyngeal cis-regulatory elements. These distinct levels of divergence presumably reflect constraints that are not clearly associated with gene function or position within the regulatory network. Thus, levels of cis-regulatory divergence or drift appear to be governed by distinct structural constraints that will be difficult to predict based on network architectur

Variable Levels Of Drift In Tunicate Cardiopharyngeal Gene Regulatory Elements

Background: Mutations in gene regulatory networks often lead to genetic divergence without impacting gene expression or developmental patterning. The rules governing this process of developmental systems drift, including the variable impact of selective constraints on different nodes in a gene regulatory network, remain poorly delineated. Results: Here we examine developmental systems drift within the cardiopharyngeal gene regulatory networks of two tunicate species, Corella inflata and Ciona robusta. Cross-species analysis of regulatory elements suggests that trans-regulatory architecture is largely conserved between these highly divergent species. In contrast, cis-regulatory elements within this network exhibit distinct levels of conservation. In particular, while most of the regulatory elements we analyzed showed extensive rearrangements of functional binding sites, the enhancer for the cardiopharyngeal transcription factor FoxF is remarkably well-conserved. Even minor alterations in spacing between binding sites lead to loss of FoxF enhancer function, suggesting that bound trans-factors form position-dependent complexes. Conclusions: Our findings reveal heterogeneous levels of divergence across cardiopharyngeal cis-regulatory elements. These distinct levels of divergence presumably reflect constraints that are not clearly associated with gene function or position within the regulatory network. Thus, levels of cis-regulatory divergence or drift appear to be governed by distinct structural constraints that will be difficult to predict based on network architecture