WHAT DO WE KNOW ABOUT CHAROPHYTE (STREPTOPHYTA) LIFE CYCLES?1

The charophyte algae are the closest living relatives of land plants. Their life cycles are usually characterized as haploid with zygotic meiosis. This conclusion, however, is based on a small number of observations and on theoretical assumptions about what kinds of life cycle are possible. Little is known about the life cycles of most charophytes, but unusual phenomena have been reported in comparatively well‐studied taxa: Spirogyra and Sirogonium are reported to produce diploid gametes with synapsis of homologous chromosomes before fusion of gametic nuclei; Closterium ehrenbergii is reported to undergo chromosome reduction both before and after syngamy; and zygotes of Coleochaete scutata are reported to replicate their DNA to high levels before a series of reduction divisions. All of these phenomena require confirmation, as does the conventional account.     

WHAT SHALL WE DO WITH THE BLUE-GREEN COUNTERPARTS?

Lichens are troublesome organisms for taxonomists because of their special ‘ double nature ’, i.e. being composed (normally) of two partners. Only recently has it been understood properly that the same fungus can take different photosynthetic partners and develop into quite different-looking organisms, for exampleLobaria amplissimaandDendriscocaulon umhausense. The taxonomic problem is to show that two totally different-looking lichens in fact contain the same fungus. This is possible to demonstrate when mixed stands are available, but is now best done with molecular methods. Since the international code of nomenclature rules that the name of a lichen species is the name of the fungus, two different organisms with the same fungus must under the Code carry the same name, which is most impractical. To remove this unintentional complication, one must either make an exception in the Code for these cases, or establish an informal system to take care of them. The latter seems to be preferable.     

NUTRIENTS IN AFRICAN LAKE ECOSYSTEMS: DO WE KNOW ALL?

SUMMARY

It is nearly sixty years since the first studies were undertaken on the nutrient chemistry of African lakes. There have been numerous studies on the chemical composition of African waters in the intervening years. Yet as recently as five years ago it was stated that little was known about nutrient cycling in lakes. Nutrient ‘species’ simply formed an additional list compiled along with lists of species of algae, zooplankton, aquatic plants and fish. A spate of monographs, papers and reports in recent years, however, has begun to fill some of the gaps in our knowledge of nutrient cycling in African lake ecosystems. This paper reviews the recent literature of nutrients in African lakes from the point of view of nutrient sources, in-lake nutrient kinetics and nutrient sinks, with particular reference to nitrogen and phosphorus, and their cycling rates into and out of various biotic and abiotic compartments. The principle conclusions that can be drawn from the review are as follows:

1. Allochthonous inputs, particularly in terms of external nutrient loading, have been relatively well-studied in recent years, but little is known of autochthonous nutrient inputs, despite numerous observations that nutrient regeneration is likely to be substantial in African lakes.

2. The rôle of microbial processes in nutrient cycling in African lakes is almost totally unknown, except in relation to nitrification and denitrification.

3. Recent studies have begun to examine the kinetics of the uptake of phosphorus by algae in African lakes; nitrogen uptake, other than nitrification, and nutrient release have only rarely been examined.

4. Nutrient uptake and release by aquatic macrophytes is reasonably well known, especially in the ‘nuisance’ weed species.

5. The role of zooplankton, zoobenthos and fish in nutrient cycling in African lakes has largely been ignored.

6. A great deal of study has been devoted to the rôle of abiotic process, particularly at the sediment-water interface, in the nutrient dynamics of African lakes.

As yet, little emphasis has been placed on inter-compartmental exchanges in studies on nutrient cycles but it would appear that these processes are now beginning to receive attention and, as nutrient cycling in African lake ecosystems becomes better known, research will tend toward a more numerical approach.     

THE ISSUE OF ANTIBIOTIC USE IN THE LIVESTOCK INDUSTRY: WHAT HAVE WE LEARNED?

It is generally believed that it is better to use medicinal products as therapeutics to treat disease situations, using high doses for short periods of time, rather than as prophylactics, when low doses are fed continuously. It is therefore the continuous use of low levels of medicinal products as growth promoters in farm animals that has been brought into question, as it is thought that this may increase the risk of development of bacterial resistance to antibiotics used as therapeutic drugs to treat disease in humans.     

WHAT USES ARE MATING TYPES? THE “DEVELOPMENTAL SWITCH” MODEL

Why mating types exist at all is subject to much debate. Among hypotheses, mating types evolved to control organelle transmission during sexual reproduction, or to prevent inbreeding or same-clone mating. Here I review data from a diversity of taxa (including ciliates, algae, slime molds, ascomycetes, and basidiomycetes) to show that the structure and function of mating types run counter the above hypotheses. I argue instead for a key role in triggering developmental switches. Genomes must fulfill a diversity of alternative programs along the sexual cycle. As a haploid gametophyte, an individual may grow vegetatively (through haploid mitoses), or initiate gametogenesis and mating. As a diploid sporophyte, similarly, it may grow vegetatively (through diploid mitoses) or initiate meiosis and sporulation. Only diploid sporophytes (and not haploid gametophytes) should switch on the meiotic program. Similarly, only haploid gametophytes (not sporophytes) should switch on gametogenesis and mating. And they should only do so when other gametophytes are ready to do the same in the neighborhood. As argued here, mating types have evolved primarily to switch on the right program at the right moment.     

RECONNECTING CELL AND ANIMAL LINEAGES: WHAT DO CELL LINEAGES TELL US ABOUT THE EVOLUTION AND DEVELOPMENT OF SPIRALIA?

Cell lineage studies in the clade Eutrochozoa, and especially the Spiralia, remains a rich and relatively untapped source for understanding broad evolutionary developmental problems; including (1) the utility of cell timing formation for phylogenetic hypotheses; (2) the evolution of cell timing changes and its relation to heterochronic patterns; (3) stereotypy or lack thereof in rates of change of cell growth during evolution and its relation to both evolutionary history and current usage; and (4) how mosaic cleavage timing variation may be expected to differ from other groups. A compilation of available cell timing information was made from previous studies where each division was explicitly followed and the total number of cells followed was greater than 24. From that compilation, we performed a series of heuristic and quantitative analyses, including a phylogenetic analysis using cell timing data as characters and analyses of timing variation across all taxa. Our results show that: (1) cell lineage data reconstructs a phylogenetic hypothesis that has similarities, especially among the Mollusca. to the patterns found in morphological and molecular analyses; (2) the mesentoblast (4d) is a unique cell compared to other cell in that it speeds up and slows down relative to other cells in taxa with both unequal and equal cell sizes; (3) some cells that form in the same quartet at the same point in the cell lineage hierarchy have much lower variations than analogous other cells, arguing for architectural constraint or stabilizing selection acting on those cells; and (4) although variation in cell timing generally increases during development, timing of formation of progeny cells in the first quartet has lower variation than the parent cells, arguing that some regulation-like behavior might be present.     

WHAT DO ISLAMIC INSTITUTIONAL FATWAS SAY ABOUT MEDICAL AND RESEARCH CONFIDENTIALITY AND BREACH OF CONFIDENTIALITY?

Protecting confidentiality is an essential value in all human relationships, no less in medical practice and research.(1) Doctor-patient and researcher-participant relationships are built on trust and on the understanding those patients' secrets will not be disclosed.(2) However, this confidentiality can be breached in some situations where it is necessary to meet a strong conflicting duty.(3) Confidentiality, in a general sense, has received much interest in Islamic resources including the Qur'an, Sunnah and juristic writings. However, medical and research confidentiality have not been explored deeply. There are few fatwas about the issue, despite an increased effort by both individuals and Islamic medical organizations to use these institutional fatwas in their research. Infringements on confidentiality make up a significant portion of institutional fatwas, yet they have never been thoroughly investigated. Moreover, the efforts of organizations and authors in this regard still require further exploration, especially on the issue of research confidentiality. In this article, we explore medical and research confidentiality and potential conflicts with this practice as a result of fatwas released by international, regional, and national Islamic Sunni juristic councils. We discuss how these fatwas affect research and publication by Muslim doctors, researchers, and Islamic medical organizations. We argue that more specialized fatwas are needed to clarify Islamic juristic views about medical and research confidentiality, especially the circumstances in which infringements on this confidentiality are justified.     

THE LICHEN SYMBIOSIS—WHAT IS SO SPECTACULAR ABOUT IT?

Lichen mycobionts are typical representatives of their fungal classes but differ from non-lichenized taxa by their manifold adaptations to symbiosis with a population of minute photobiont cells. Most interesting are the morphologically complex macrolichens, the fungal partner of which competes for space above ground and contains photobiont cells optimally positioned for gas exchange and illumination. Such thalli are the product of an amazing hyphal polymorphism, with multiple switches between polar and apolar growth and hydrophilic or hydrophobic cell wall surfaces. Hydrophobic sealing of the apoplastic continuum between the partners by means of mycobiont-derived hydrophobic compounds canalizes the fluxes of solutes during the often quite dramatic de- and rehydration processes and keeps the algal layer gas-filled at any level of hydration. The impressive tolerance of drought, heat and cold stress of most lichen-forming fungi and their photobionts is due to a very interesting combination of protective and repair mechanisms at the cellular level, the molecular bases of which remain to be explored. Contemporary experimental lichenology is analysed and strategies are proposed aimed at better integration into mainstream biology.     

WHAT IS THE GOOD OF HEALTH CARE?

This paper sets out to discuss what precisely is meant by 'benefit" when we talk of the requirement that the health care system concern itself with health gain or with maximizing beneficial health care. In particular I argue that in discharging the duty to do what is most beneficial we need to choose between rival conceptions of what is meant by beneficial. One is the patient's conception of benefit and the second is the provider's or funder's conception of benefit. I argue that it is the patient's conception of benefit which is paramount and that if this is followed it commits us to a conception of patient care which must be blind to prognosis in so far as prognosis is thought to bear upon issues of prioritisation or resource allocation.     

WHAT CAN MULTIPLE PHYLOGENIES SAY ABOUT THE LATITUDINAL DIVERSITY GRADIENT? A NEW LOOK AT THE TROPICAL CONSERVATISM,OUT OF THE TROPICS,AND DIVERSIFICATION RATE HYPOTHESES

We reviewed published phylogenies and selected 111 phylogenetic studies representing mammals, birds, insects, and flowering plants. We then mapped the latitudinal range of all taxa to test the relative importance of the tropical conservatism, out of the tropics, and diversification rate hypotheses in generating latitudinal diversity gradients. Most clades originated in the tropics, with diversity peaking in the zone of origin. Transitions of lineages between latitudinal zones occurred at 16–22% of the tree nodes. The most common type of transition was range expansions of tropical lineages to encompass also temperate latitudes. Thus, adaptation to new climatic conditions may not represent a major obstacle for many clades. These results contradict predictions of the tropical conservatism hypothesis (i.e., few clades colonizing extratropical latitudes), but support the out‐of‐the‐tropics model (i.e., tropical originations and subsequent latitudinal range expansions). Our results suggest no difference in diversification between tropical and temperate sister lineages; thus, diversity of tropical clades was not explained by higher diversification rates in this zone. Moreover, lineages with latitudinal stasis diversified more compared to sister lineages entering a new latitudinal zone. This preserved preexisting diversity differences between latitudinal zones and can be considered a new mechanism for why diversity tends to peak in the zone of origin.