Immunohistochemical localisation of chondroitin sulphate proteoglycans and the effects of chondroitinase ABC in 9- to 11-day rat embryos

Studies on cell behaviour in vitro have indicated that the chondroitin sulphate proteoglycan (CSPG) family of molecules can participate in the control of cell proliferation, differentiation and adhesion, but its morphogenetic functions had not been investigated in intact embryos. Chondroitin/chondroitin sulphates have been identified in rat embryos at low levels at the start of neurulation (day 9) and at much higher levels on day 10. In this study we have sought evidence for the morphogenetic functions of CSPGs in rat embryos during the period of neurulation and neural crest cell migration by a combination of two approaches: immunocytochemical localization of CSPG by means of an antibody, CS-56, to the chondroitin sulphate component of CSPG, and exposure of embryos to the enzyme chondroitinase ABC. Staining of the CS-56 epitope was poor at the beginning of cranial neurulation; bright staining was at first confined to the primary mesenchyme under the convex neural folds late on day 9. In day 10 embryos, all mesenchyme cells were stained, but at different levels of intensity, so that primary mesenchyme, neural crest and sclerotomal cells could be distinguished from each other. Basement membranes were also stained, particularly bright staining being present where two epithelial were basally apposed, e.g., neural/surface ectoderms, dorsal aorta/neural tube, prior to migration of a population of cells between them. Staining within the neural epithelium was first confined to the dorsolateral edge region, and associated with the onset of neural crest cell emigration; after neural tube closure, neuroepithelial staining was more general. Neural crest cells were stained during migration, but the reaction was absent in areas associated with migration end-points (trigeminal ganglion anlagen, frontonasal mesenchyme). Embryos exposed to chondroitinase ABC in culture showed no abnormalities until early day 10, when cranial neural crest cell emigration from the neural epithelium was inhibited and neural tube closure was retarded. Sclerotomal cells failed to take their normal pathway between the dorsal aorta and neural tube. Correlation of the results of these two methods suggests: (1) that by decreasing adhesiveness within the neural epithelium at specific stages, CSPG facilitates the emigration of neural crest cells and the migratory movement of neuroblasts, and may also provide increased flexibility during the generation of epithelial curvatures; (2) that by decreasing the adhesiveness of fibronectin-containing extracellular matrices, CSPG facilitates the migration of neural crest and sclerotomal cells. This second function is particularly important when migrating cells take pathways between previously apposed tissues.     

A new type of specialized morphophysiological dormancy and seed storage behaviour in Hydatellaceae, an early-divergent angiosperm family

Background and Aims

Recent phylogenetic analysis has placed the aquatic family Hydatellaceae as an early-divergent angiosperm. Understanding seed dormancy, germination and desiccation tolerance of Hydatellaceae will facilitate ex situ conservation and advance hypotheses regarding angiosperm evolution.

Methods

Seed germination experiments were completed on three species of south-west Australian Hydatellaceae, Trithuria austinensis, T. bibracteata and T. submersa, to test the effects of temperature, light, germination stimulant and storage. Seeds were sectioned to examine embryo growth during germination in T. austinensis and T. submersa.

Key Results

Some embryo growth and cell division in T. austinensis and T. submersa occurred prior to the emergence of an undifferentiated embryo from the seed coat (‘germination’). Embryo differentiation occurred later, following further growth and a 3- to 4-fold increase in the number of cells. The time taken to achieve 50 % of maximum germination for seeds on water agar was 50, 35 and 37 d for T. austinensis, T bibracteata and T. submersa, respectively.

Conclusions

Seeds of Hydatellaceae have a new kind of specialized morphophysiological dormancy in which neither root nor shoot differentiates until after the embryo emerges from the seed coat. Seed biology is discussed in relation to early angiosperm evolution, together with ex situ conservation of this phylogenetically significant group.     

Nonflowers near the base of extant angiosperms? Spatiotemporal arrangement of organs in reproductive units of Hydatellaceae and its bearing on the origin of the flower

Reproductive units (RUs) of Trithuria, the sole genus of the early-divergent angiosperm family Hydatellaceae, are compared with flowers of their close relatives in Cabombaceae (Nymphaeales). Trithuria RUs combine features of flowers and inflorescences. They differ from typical flowers in possessing an "inside-out" morphology, with carpels surrounding stamens; furthermore, carpels develop centrifugally, in contrast to centripetal or simultaneous development in typical flowers. Trithuria RUs could be interpreted as pseudanthia of two or more cymose partial inflorescences enclosed within an involucre, but the bractlike involucral phyllomes do not subtend partial inflorescences and hence collectively resemble a typical perianth. Teratological forms of T. submersa indicate a tendency to fasciation and demonstrate that the inside-out structure-the primary feature that separates RUs of Hydatellaceae from more orthodox angiosperm flowers-can be at least partially modified, thus producing a morphology that is closer to an orthodox flower. The Trithuria RU could be described as a "nonflower", i.e., a structure that contains typical angiosperm carpels and stamens but does not allow recognition of a typical angiosperm flower. The term nonflower could combine cases of secondary loss of flower identity and cases of a prefloral condition, similar to those that gave rise to the angiosperm flower. Nonhomology among some angiosperm flowers could be due to iterative shifts between nonfloral construction and flower/inflorescence organization of reproductive organs. Potential testing of these hypotheses using evolutionary-developmental genetics is explored using preliminary data from immunolocalization of the floral meristem identity gene LEAFY in T. submersa, which indicated protein expression at different hierarchical levels.     

Study of envelope proteins in E. coli cet and recA mutants by SDS acrylamide gel electrophoresis

Disc-electrophoresis of E. coli envelope proteins on SDS acrylamide gels reproducibly revealed up to 50 distinct polypeptide bands. Corresponding molecular weights ranged from 105,000 to 20,000 daltons or less. Major bands corresponded to molecular weights of 73,000, 48,000, 36,000 and 30,000 with the latter constituting up to 20% of the total envelope protein depending upon the method of isolation. Minimum levels of detection using stained gels equaled 0.25 μg protein or 1% of total sample analyzed; for a polypeptide of molecular weight 40,000 daltons this was calculated to be equivalent to 1,200 molecules per cell envelope. In envelopes from a cetB^? mutant strain (refractory to colicin E2), an additional band, constituting up to 5% of the total envelope protein was present. The molecular weight of this protein, which was maximally present in wild type envelopes in only trace amounts, is 44,000 daltons, indicating a cellular concentration of approximately 6 × 10³ molecules per envelope. This new band was not affected by heating envelope preparations to 100° prior to electrophoresis, but was largely eliminated by washing isolated envelopes in low ionic strength buffer, or by pre-incubating cells with trypsin prior to preparation of envelopes. Treatment of isolated envelopes with Triton X-100, which preferentially releases inner membrane proteins from the envelope (18), resulted in the extraction of a preponderance of the high molecular weight polypeptides, including the 44,000 dalton protein from envelopes of the mutant. The major polypeptides of the envelope and the low molecular weight components were not extracted by Triton X-100. The properties of the 44,000 dalton protein indicated that it is relatively loosely associated with the surface envelope and may be exposed on the external surface of the cytoplasmic membrane. Possible explanations for the appearance of this protein in mutant strains and its relationship to the inability of these to respond, specifically to surface bound colicin E2, will be discussed. Extensive analysis of envelopes from recA^? mutants was also carried out and revealed an unusual amount of variation in polypeptide profiles obtained from different preparations. However, no consistent quantitative or qualitative difference between recA and rec⁺ strains was obtained. In recA, cetB double mutants, the increased level of the 44,000 dalton polypeptide was identical to that found in the rec⁺, cetB mutant.     

Non-native poeciliids in hot water: the role of thermal springs in facilitating invasion of tropical species

Hydrobiologia - Livebearers in the family Poeciliidae are some of the most widely introduced fishes. Native poeciliid translocations within the U.S. are mostly due to deliberate stocking for...     

Coastal wetland restoration improves habitat for juvenile sportfish in Tampa Bay,Florida, U.S.A.

Increasing human populations and urban development have led to losses of estuarine habitats for fish and wildlife. Where resource managers are restoring coastal wetlands, in addition to meeting goals related to hydrologic connectivity, biodiversity, and recreational opportunities, efforts are being made to provide habitat that is suitable for juvenile sportfish. An 18‐month study was conducted to compare juvenile sportfish use of natural, restored, and impacted sites along Tampa Bay, Florida, shorelines. Juvenile sportfish densities at restored sites were broadly comparable to natural sites and greater than at impacted sites. However, site‐specific differences in sportfish use did occur within site types. For example, one restored site had significantly higher densities of red drum Sciaenops ocellatus than any other site, while black drum Pogonias cromis were found exclusively at another restored site. To evaluate whether the restored sites are providing suitable habitat for juvenile fish, we assessed growth (estimated from counts of daily rings on otoliths) and condition (determined by lipid analyses) of juvenile common snook Centropomus undecimalis, an archetypal coastal wetland‐dependent species. Growth (0.43–0.56 mm SL/day) and condition (4.6–6.1% lipid of dry weight) exhibited only site‐specific differences and did not vary among natural, restored, and impacted site types. Although mortality rates of juvenile sportfish were not determined, use of a 40‐m seine found that densities of potential piscine predators in these coastal wetlands were relatively low compared to published studies of open estuarine shorelines. The restoration and creation of coastal wetlands in Tampa Bay provides improved habitat for juvenile sportfish.     

Comparative ovule and megagametophyte development in Hydatellaceae and water lilies reveal a mosaic of features among the earliest angiosperms

Background and Aims: The embryo sac, nucellus and integuments of the early-divergentangiosperms Hydatellaceae and other Nymphaeales are comparedwith those of other seed plants, in order to evaluate the evolutionaryorigin of these characters in the angiosperms. Methods: Using light microscopy, ovule and embryo sac development aredescribed in five (of 12) species of Trithuria, the sole genusof Hydatellaceae, and compared with those of Cabombaceae andNymphaeaceae. Key Results: The ovule of Trithuria is bitegmic and tenuinucellate, ratherthan bitegmic and crassinucellate as in most other Nymphaeales.The seed is operculate and possesses a perisperm that developsprecociously, which are both key features of Nymphaeales. However,in the Indian species T. konkanensis, perisperm is relativelypoorly developed by the time of fertilization. Perisperm cellsin Trithuria become multinucleate during development, a featureobserved also in other Nymphaeales. The outer integument issemi-annular (‘hood-shaped’), as in Cabombaceaeand some Nymphaeaceae, in contrast to the annular (‘cap-shaped’)outer integument of some other Nymphaeaceae (e.g. Barclaya)and Amborella. The megagametophyte in Trithuria is monosporicand four-nucleate; at the two-nucleate stage both nuclei occurin the micropylar domain. Double megagametophytes were frequentlyobserved, probably developed from different megaspores of thesame tetrad. Indirect, but strong evidence is presented forapomictic embryo development in T. filamentosa. Conclusions: Most features of the ovule and embryo sac of Trithuria are consistentwith a close relationship with other Nymphaeales, especiallyCabombaceae. The frequent occurrence of double megagametophytesin the same ovule indicates a high degree of developmental flexibility,and could provide a clue to the evolutionary origin of the Polygonum-typeof angiosperm embryo sac.