A functional morphospace for the skull of labrid fishes: patterns of diversity in a complex biomechanical system

The Labridae (including wrasses, the Odacidae and the Scaridae) is a species‐rich group of perciform fishes whose members are prominent inhabitants of warm‐temperate and tropical reefs worldwide. We analyse functionally relevant morphometrics for the feeding apparatus of 130 labrid species found on the Great Barrier Reef and use these data to explore the morphological and mechanical basis of trophic diversity found in this assemblage. Morphological measurements were made that characterize the functional and mechanical properties of the oral jaws that are used in prey capture and handling, the hyoid apparatus that is used in expanding the buccal cavity during suction feeding, and the pharyngeal jaw apparatus that is used in breaking through the defences of shelled prey, winnowing edible matter from sand and other debris, and pulverizing the algae, detritus and rock mixture eaten by scarids (parrotfishes). A Principal Components Analysis on the correlation matrix of a reduced set of ten variables revealed complete separation of scarids from wrasses on the basis of the former having a small mouth with limited jaw protrusion, high mechanical advantage in jaw closing, and a small sternohyoideus muscle and high kinematic transmission in the hyoid four‐bar linkage. Some scarids also exhibit a novel four‐bar linkage conformation in the oral jaw apparatus. Within wrasses a striking lack of strong associations was found among the mechanical elements of the feeding apparatus. These weak associations resulted in a highly diverse system in which functional properties occur in many different combinations and reflect variation in feeding ecology. Among putatively monophyletic groups of labrids, the cheilines showed the highest functional diversity and scarids were moderately diverse, in spite of their reputation for being trophically monomorphic and specialized. We hypothesize that the functional and ecological diversity of labrids is due in part to a history of decoupled evolution of major components of the feeding system (i.e. oral jaws, hyoid and pharyngeal jaw apparatus) as well as among the muscular and skeletal elements of each component. © 2004 The Linnean Society of London, Biological Journal of the Linnean Society, 2004, 82 , 1–25.     

Resurrection Plants and the Secrets of Eternal Leaf

Most higher plants possess a phase in their life cycle in whichtissues can survive desiccation. However, this is restrictedto specialized tissues such as seeds and pollen. Resurrectionplants are remarkable in that they can tolerate almost completewater loss in their vegetative tissues. The desiccated plantcan remain alive in the dried state for several years. However,upon watering the plants rehydrate and are fully functionalwithin 48 h. Underpinning this amazing ability is the capacityto accumulate large amounts of sucrose in the tissues. Thissugar has the property of stabilizing enzymes and cellular structuresin the absence of water. The sources of carbon that fuel sucrosesynthesis are not known, but temporary carbohydrate stores andphotosynthesis are the most likely candidates. On rewatering,the sucrose is metabolized rapidly as the tissues rehydrate.Increased expression of a number of genes in response to droughtstress have been noted. A number of these are associated withmetabolic pathways linked with primary carbohydrate metabolism.However, some genes related to LEA (Late Embryogenic Abundant)proteins have been isolated which suggests they too may playa role in maintaining tissue integrity during desiccation. Howthese mechanisms are integrated to enable resurrection plantsto survive desiccation is discussed. Copyright 2000 Annals ofBotany Company ABA, Craterostigma, desiccation tolerance, poikilohydric, resurrection.     

The Membranes of a Eukaryotic Cell

The evolution of internal membrane systems has introduced manyadditional control steps into pathways that, although basicallysimilar in prokaryotic cells, are less sophisticated and leavemany aspects up to chance. Temporal and spatial control of secretion,quality control of the proteins secreted or inserted into theplasma membrane, and exquisite control over the selective degradationof macromolecules, for example, are apparently indispensiblerequirements in multicellular organisms, but are relativelyunimportant in bacteria. Although complicated in detail, mostmembrane traffic in the eukaryotic cell can be reduced to afew basic principles. Such a reductionist's view provides aconceptual framework that allows the reader to organize an otherwiseoverwhelming amount of data on cellular membrane architectureand dynamics.     

Does Late-acting Self-incompatibility (LSI) Show Family Clustering? Two More Species of Bignoniaceae with LSI:Dolichandra cynanchoides and Tabebuia nodosa

By means of hand pollination experiments and fluorescence microscopythe breeding systems and pollen tube growth were studied inDolichandra cynanchoides and Tabebuia nodosa, two bignoniaceousspecies of the Chaco woodland of NE Argentina. Both speciesabscised all selfed pistils within 4–8 d although selfpollen tubes grew successfully to the ovary and penetrated manyovules. Both species therefore show ‘late-acting self-incompatibility’(LSI) or ‘ovarian sterility’ (OS) type control ofselfing. LSI-OS has been reported in 17 species of the Bignoniaceae,and is also clustered in families such as the Bombacaceae-Sterculiaceae,Fabaceae and Myrtaceae. The implications of such family clusteringare discussed, with regard to current hypotheses for the actionof LSI-OS phenomena. Copyright 1999 Annals of Botany Company Bignoniaceae, Dolichandra cynanchoides, Tabebuia nodosa, Chaco, late-acting self-incompatibility, ovarian sterility.     

Covert Categories and Folk Taxonomies

Much of the recent work in ethnoscience has been concerned with the nature of folk taxonomies, an often stated definition of which requires that all folk taxa be monolexemically labeled. This paper offers evidence that unlabeled categories may also be of crucial taxonomic significance, and we feel that it is inappropriate to treat such categories apart from the named taxonomic entities of the system. More importantly, evidence presented indicates that by recognizing unnamed taxa one may gain an understanding of the structure of a particular semantic domain that is actually obscured if one focuses solely on lexically labeled units.     

Phosphatized soft-bodied squids from the Jurassic Oxford Clay

A diagenetic case study of phosphatized soft-bodied squids from the lower part of the Oxford Clay of Christian Malford, Wiltshire, has dated mineralization in relation to burial history. Complete squids with mantle tissues were examined under the SEM as uncoated specimens at low KV. A simple stage attachment designed for this purpose is described. Soft-parts are preserved in three dimensions and must therefore have been mineralized prior to decay-induced tissue collapse. Such mineralization occurred near to the anoxic/oxic boundary in the 'soupy' upper layer of organic-rich sediment. In acrobic conditions, phosphates were liberated to pore-water solution from decomposing organic matter and became adsorbed to ferric hydroxides within sediment. The reduction of these ferric hydroxides at the anoxic-oxic interface liberated phosphates to solutions which were conccntrated in the decomposing carcasses of the squids. This mineral concentration was favoured by the development of a high pH reducing environment around the carcass and possibly by complexing with protcolipids liberated by decomposition of animal matter. ▭ Soft-part preservation, phosphatization, SEM techniques, cephatopod. Oxford Clay, Wiltshire, England.     

Use of precision cut human liver slices for studying the metabolism and genotoxic potential of xenobiotics by means of the 32P-postlabelling technique: steps towards method validation using testosterone and 2-aminofluorene

In the present study, a new in vitro model combining the short-term incubation of precision-cut human liver slices with DNA-adduct analysis by the ³²P-postlabelling technique is proposed for investigation of the genotoxic potential of xenobiotics. For method validation, the metabolic turnover of testosterone (TES) and the DNA-adduct inducing potential of 2-aminofluorene (2-AF) were used. Precision-cut human liver slices were prepared from a total of 12 human liver samples which were freshly obtained as parts of resectates from liver surgery. The slices were incubated as submersion cultures with TES and 2-AF for up to 6 h in 12-well tissue culture plates at concentrations of 10-50 and 0.06-28 μM, respectively. Slices recovered from the slicing procedure in the 4 °C cold Krebs-Henseleit buffer as indicated by intracellular potassium concentrations which increased for 2 h and then remained stable until the end of the incubation. TES was extensively metabolized by human liver slices with a similar metabolite pattern as observed in vivo. Almost 90% of the metabolites were conjugates. Major phase-I metabolites were androstendione, 6β-OH-androstendione, 6β-OH-TES, and 15β-OHTES. After incubation with 2-AF, substance related DNA-adducts were detected which increased dose-dependently from 12 to 1146 adducts per 10⁹ nucleotides. The adduct pattern consisted of one major adduct spot, A, representing 80-90% of the total adduct level and up to four minor adduct spots, B-E. In summary, the present data demonstrate that precision-cut liver slices are a valuable alternative in vitro system for DNA-adduct determination to screen chemicals for potential genotoxicity in humans.