Paedomorphosis in two small species of toothed whales (Odontoceti): how and why?

To evaluate and assess the ontogenetic background for paedomorphosis in phocoenids, samples of 144 harbour porpoises, 81 white‐beaked dolphins, and 130 Commerson's dolphins were compared in terms of the development of epiphyseal fusion, cranial suture fusion, and ontogeny of cranial shape. Harbour porpoises and Commerson's dolphins terminated growth and development of all investigated traits sooner than white‐beaked dolphins, leading to lesser degrees of fusion of skeletal elements and less postnatal allometric development. The latter occurred even though shape in the two paedomorphic species developed at twice the rate relative to the size of white‐beaked dolphins. These observations imply that progenetic evolution has occurred convergently in phocoenid and Cephalorhynchus ancestors. The truncated ontogenies allow sexual maturity to be attained earlier and provide a greater reproductive potential. Both species inhabit similar temperate productive habitats and, hence, ecological factors are proposed to have supplied the selection pressures leading to progenesis. Constant prey availability must be a prerequisite for the observed phenomena because frequent food‐intake is necessitated by the limited capacity for energy storage and high heat‐loss entailed by the resulting small body sizes. Progenesis has rarely been proposed in mammal species. This may reflect rarity or that mammalian expressions of progenesis are less obvious. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99 , 278–295.     

Pelagic and benthic net production of dissolved inorganic carbon in an unproductive subarctic lake

1. Both the pelagic and benthic net dissolved inorganic carbon (DIC) productions were measured in situ on four occasions from June to September 2004, in the unproductive Lake Diktar-Erik in subarctic Sweden. The stable isotopic signal ( δ ¹³C) of respired organic material was estimated from hypolimnion water data and data from a laboratory incubation using epilimnion water.
2. Both pelagic and benthic habitats were net heterotrophic during the study period, with a total net DIC production of 416 mg C m⁻² day⁻¹, of which the pelagic habitat contributed approximately 85%. The net DIC production decreased with depth both in the pelagic water and in the sediments, and most of the net DIC production occurred in the upper water column.
3. Temporal variations in both pelagic and benthic DIC production were small, although we observed a significant decrease in pelagic net DIC production after the autumn turnover. Water temperature was the single most important factor explaining temporal and vertical variations in pelagic DIC production. No single factor explained more than 10% of the benthic net DIC production, which probably was regulated by several interacting factors.
4. Pelagic DIC production, and thus most of the whole-lake net production of DIC, was mainly due to the respiration of allochthonous organic carbon. Stable isotope data inferred that nearly 100% of accumulated DIC in the hypolimnion water had an allochthonous carbon source. Similarly, in the laboratory incubation using epilimnion water, c. 85% of accumulated DIC was indicated to have an allochthonous organic carbon source.     

Editor's column: Planktic, nektic, benthic

The terms planktic, nektic , and benthic are taken as examples of the construction and malconstruction of biological and geological terms. Both in vernacular terminology and systematic nomenclature the formation of adjectives and compounds follows the same basic rules - keep the three concepts of stem, suffix, and connective vowel clear, and most of the serious malconstructions will be avoided.     

Editor's column: Nemagraptus, Pelekysgnathus, Foramenella

Systematic nomenclature follows the same rules for compounding and derivation as the scientific terminology discussed in a preceding Editor's Column. Lethaia honours appealing and correctly constructed names (and terms), but the codes of biological nomenclature do not in practice permit 'justified emendations' of names which do not meet the linguistic requirements in the same codes - in practice priority in 'spelling' supersedes correctness in 'language'. Construction of systematic names is easy, and the introduction of further incorrect and mnemonically cumbersome forms is easily curbed by requiring a statement on the derivation of each new name, scrutinized by a linguist if necessary.     

The cost of secondary sexual characters and the evolution of cost-reducing traits

Secondary sexual traits are characterized by their exaggerated expression relative to homologous nonsexual characters in other species. All models of sexual selection assume that sex traits are costly to produce and maintain, and individuals with reduced costs of production and maintenance of secondary sexual characters would be at a selective advantage. A number of morphological, physiological and behavioural traits may have evolved as a result of their cost-reducing properties: (1) body size, which does not change throughout life, that allows certain individuals to develop exaggerated sex traits, (2) cost-reducing traits, such as muscle size, that improve with practice and (3) actual cost-reducing traits, such as wing size in birds with song flight, which are produced in advance of or simultaneously with the sex trait. Cost-reducing traits may coevolve with secondary sexual characters and allow more extreme sexual signalling than would otherwise have been possible in their absence or in reduced versions.