ABSTRACT
Persistent institutionalized inequality (PII) emerged at the Bridge River site by ca 1200-1300 years ago. Research confirms that PII developed at a time of population packing associated with unstable fluctuations in a critical food resource (anadromous salmon) and persisted across multiple generations. While we understand the demographic and ecological conditions under which this history unfolded, we have yet to address details of the underlying social process. In this paper, we draw on Bridge River's Housepit 54 to examine two alternative hypotheses. Hypothesis 1, mutualism, suggests that household heads signalled to maintain and attract new members as a means of supporting the demographic viability of the house. Inequality is indicated by variation in prestige markers but less obviously in economic fundamentals. Hypothesis 2, coercion, asserts that the more successful households developed control over access to critical food resources, forcing others into the choice between emigration and subjugation. Inequality is indicated by inter-family differences in prestige markers and economic fundamentals. Results suggest that inequality emerged under a mutualism scenario but persisted for subsequent generations under more coercive conditions. This article is part of the theme issue 'Evolutionary ecology of inequality'.
Subject(s)
Coercion , Symbiosis , British Columbia , Biological Evolution , RiversABSTRACT
Great transitions are thought to embody major shifts in locus of selection, labour diversification and communication systems. Such expectations are relevant for biological and cultural systems as decades of research has demonstrated similar dynamics within the evolution of culture. The evolution of the Neo-Inuit cultural tradition in the Bering Strait provides an ideal context for examination of cultural transitions. The Okvik/Old Bering Sea (Okvik/OBS) culture of Bering Strait is the first representative of the Neo-Inuit tradition. Archaeological evidence drawn for settlement and subsistence data, technological traditions and mortuary contexts suggests that Okvik/OBS fits the definition of a major transition given change in the nature of group membership (from families to political groups with social ranking), task organization (emergent labour specialization) and communication (advent of complex art forms conveying social and ideological information). This permits us to develop a number of implications about the evolutionary process recognizing that transitions may occur on three scales: (1) ephemeral variants, as for example, simple technological entities; (2) integrated systems, spanning modular technology to socio-economic strategies; and (3) simultaneous change across all scales with emergent properties. This article is part of the theme issue 'Human socio-cultural evolution in light of evolutionary transitions'.
Subject(s)
Cultural Evolution , Humans , Oceans and Seas , TechnologyABSTRACT
We have developed a strategy for synthesizing passively permeable peptidomimetic macrocycles. The cyclization chemistry centers on using aziridine aldehydes in a multicomponent reaction with peptides and isocyanides. The linker region in the resulting product contains an exocyclic amide positioned α to the peptide backbone, an arrangement that is not found among natural amino acids. This amide provides structural rigidity within the cyclic peptidomimetic and promotes the creation of a stabilizing intramolecular hydrogen bonding network. This exocyclic control element also contributes to the increased membrane permeability exhibited by multicomponent-derived macrocycles with respect to their homodetic counterparts. The exocyclic control element is employed along with a strategic placement of N-methyl and d-amino acids to produce passively permeable peptides, which contain multiple polar residues. This strategy should be applicable in the pursuit of synthesizing therapeutically relevant macrocycles.
Subject(s)
Amides/chemistry , Macrocyclic Compounds/chemistry , Amides/chemical synthesis , Macrocyclic Compounds/chemical synthesis , Molecular ConformationABSTRACT
Aziridine aldehyde dimers, peptides, and isocyanides participate in a multicomponent reaction to yield peptide macrocycles. We have investigated the selectivity and kinetics of this process and performed a detailed analysis of its chemoselectivity. While the reactants encompass all of the elements of the traditional Ugi four-component condensation, there is a significant deviation from the previously proposed mechanism. Our results provide evidence for an imidoanhydride pathway in peptide macrocyclization and lend justification for the diastereoselectivity and high effective molarity observed in the reaction.