The life cycles of cryptogams

Meiosis and karyogamy are recognized as control points in the life cycle of cryptogams. The control of meiosis is evidently complex and in yeast, and by analogy in all cryptogams, involves progressive gene activation. The causes of the delay in meiosis in diplohaplontic and diplontic organisms, and the manner in which the block is removed remain to be discovered. There is accumulating evidence that cytoplasmic RNA plays an important role in meiotic division.Many features of gametogenesis are still obscure. The tendency to oogamy has provided the opportunity for the laying down of long-lived messenger RNA in the abundant cytoplasm of the female gamete. The sporophytic nature of the developing zygote can in this way be partially pre-determined. There is evidence that this is the situation in the ferns.Specific molecules (probably arabino-galacto-proteins) on the surface of the plasma membrane are likely to account both for gametic selection, and the readiness with which appropriate gametes fuse. The dikaryotic condition indicates that nuclear fusion is not inevitable following plasmogamy. The ultimate fusion of the nuclei may result from quite simple changes in the nuclear surface. Exposure of lipid, for example, would lead to fusion as a result of hydrophobic forces.Aberrations of cryptogamic life cycles are numerous. The nuclear relationships of many aberrant cycles are unknown. In general it appears that the maintenance of sporophytic growth depends upon the presence of at least two sets of chromosomes. Conversely the maintenance of gametophytic growth in cultures obtained aposporously appears to be impossible in the presence of four sets of chromosomes, or more. These results raise important problems of the effect of gene dosage on development.La meiosis y la cariogamia son reconocidas como puntos de control en los ciclos de vida de las criptógamas. El control de la meiosis es evidentemente complejo y en levaduras, y por analogía en todas las criptógamas, incluye la activación progresiva del gen. Las causas de este retraso en la meiosis de los organismos diplohaplónticos y diplónticos y la manera en que se elimina el bloqueo aun se desconoce. Existe una acumulación de evidencias que indican que el RNA citoplásmico juega un importante papel en la división meiótica.Muchas características de la gametogénesis están aún oscuras. La tendencia hacia la oogamia ha permitido la oportunidad de establecer la longevidad del ARN mensajero en el abundante citoplasma del gameto femenino. La naturaleza del esporófito desarrollada a partir del cigoto puede ser, en este sentido, parcialmente predeterminada. Hay evidencias que esta es la situación en los helechos.La selección gamética y la prontitud con que se fusionan los gametos apropiados, probablemente se deba a moléculas específicas (quizás arabino-galacto-proteínas) de la superficie de la membrana plasmática. La condición dicariótica indica que la fusión nuclear no es inevitable como consecuencia de la plasmogamia. La fusión definitiva de los núcleos puede resultar de unos cambios bastante simples en la superfice nuclear. La exposición de lípidos, por ejemplo, conduciría a la fusión como resultado de fuerzas hidrofóbicas.Las aberraciones en el ciclo de vida de las criptógamas son numerosas. Las relaciones nucleares de muchos de los ciclos aberrantes son desconocidas. En general parece que el mantenimiento del crecimiento esporofítico depende de la presencia, por lo menos, de dos juegos de cromosomas. De manera contraria, el mantenimiento del crecimiento del gametófito en cultivos obtenidos apospóricamente parece ser imposible en presencia de cuatro juegos de cromosomas o más. Estos resultados aumentan la importancia de los problemas de la dosificación del gen en el desarrollo

A provisional survey of the interaction between net photosynthetic rate, respiratory rate, and thallus water content in some New Zealand cryptogams

The effect of water content on photosynthetic and respiratory rates in eight lichen species and one bryophyte species were studied using an injection infrared gas analyser technique. All species snowed a strong relationship between net assimilation rate (NAR), respiration rate, and water content similar to relationships reported in published studies overseas. Species from moist habitats showed negative NAR at low water contents. Species from high-light areas showed a depression in NAR at high water contents which could be alleviated by higher light intensities. The experiments confirmed the suitability of New Zealand species for these studies

The influence of tree age and microhabitat quality on the occurrence of crustose lichens associated with old oaks

Questions: How do tree age, microhabitat characteristics and epiphytic competitors affect the occurrence of crustose lichens associated with old oaks? How do microhabitat characteristics and microclimate affect the cover of competitors (bryophytes and macrolichens)? How do microhabitat characteristics cor¬relate with microclimatic variables? Location: Southeast Sweden. Methods: Eight crustose lichen species were surveyed on 165 Quercus robur trees, 17-478 years old, at three study sites. The occurrence patterns of these species were examined at two spatial scales: among trees and within trees. Occurrence patterns within trees were examined in 10 cm × 10 cm plots at all four cardinal aspects at different heights from 0.5 to 4.5 m above the ground. Results: At the tree level, age-related factors were the most important predictors of species occurrence. All species were more frequent on trees > 100 years than on younger trees. At the plot level, the frequency of occurrence increased with increasing bark crevice depth. The frequencies of all study species de¬creased with increasing cover of bryophytes. Bryophytes were in turn more frequent in plots that were exposed to rainwater and showed a low evaporation rate. Patches most exposed to rainwater were directed upwards, and the lowest evaporation rates occurred on the northern side of the trunks. Conclusions: For many crustose lichens the association with old oak trees seems at least partly to depend on their preference for the deep bark crevices that only occur on old trees. Trees represent epiphyte habitat patches that differ in size due to within-tree variability in habitat quality, such as bark crevice depth and microclimate. This study shows that variability at a finer scale, within habitat patches, contribute to explain species occurrence patterns at habitat patch level

Floristic survey of epixylic Bryophytes of an area remnant of the Atlantic forest (Timbaúba - PE, Brazil) : 1., Hepaticopsida (except Lejeuneaceae) and Bryopsida

A survey of the epixylic bryoflora of a remaining Atlantic forest (seasonal coastal deciduous forest), Engenho Água Azul, in the municipality of Timbaúba ( Lat 7° 35S; Long. 35° 20W ), State of Pernambuco, Brazil, registered 35 species of bryophytes distributed in 11 families of Bryopsida: Calymperaceae, Pilotrichaceae, Fissidentaceae, Hookeriaceae, Hypnaceae, Leucobryaceae, Leucomiaceae, Orthotrichaceae, Plagiotheciaceae, Sematophyllaceae, Thuidiaceae, and 5 of Hepaticopsida: Aneuraceae, Frullaniaceae, Geocalycaceae, Plagiochilaceae and Radulaceae. New records northeastern of Brazil are: Frullania caroliniana Sullivant, F. gymnotis Nees & Mont., Ochrobryum stenophyllum Besch., Plagiochila trigonifolia Steph., Radula macrostachya Linbenb. & Gott., Riccardia digitiloba (Spruce ex Steph.) Hell, Thuidium tomentosum Schimp. ex Besch. and Trichosteleum pusillum (Hornsch.) Jaeg. There is an indication of the description, illustration, and geographic distribution for Brazil of all taxons found.En este trabajo se presenta el catálogo de la flora briofítica epífita de la selva tropical oceánica Engenho Agua Azul, situada en el municipio de Timbaúba (Lat. 7º 35S; Long. 35º 20O), perteneciente al estado de Pernambuco, Brasil. Se registraron 35 especies de briófitos distribuidas en 11 familias de la clase Bryopsida: Calymperaceae, Pilotrichaceae, Fissidentaceae, Hookeriaceae, Hypnaceae, Leucobryaceae, Leucomiaceae, Orthotrichaceae, Plagiotheciaceae, Sematophyllaceae, Thuidiaceae y 5 de la clase Hepaticopsida: Aneuracee, Frullaniaceae, Geocalycaceae, Plagiochilaceae y Radulaceae. Se aportan nuevas citas para la región nordeste del Brasil - Frullania caroliniana Sullivant, F. gymnotis Nees & Mont., Ochrobryum stenophyllumBesch., Plagiochila trigonifoliaSteph., Radula macrostachya Linbenb. & Gott., Riccardia digitiloba(Spruce ex Steph.) Hell, Thuidium tomentosum Schimp. ex Besch. yTrichosteleum pusillum (Horsnch.) Jaeg. Se presenta una descripción y una ilustración de cada taxon y se comenta su distribución geográfica

Taxonomic results of the Bryotrop expedition to Zaire and Rwanda : 20., Grimmiaceae, Funariaceae, Bartramiaceae (Philonotis), Amblystegiaceae, Plagiotheciaceae

For worldwide monograph see Bremer (1980a, b, 1981). Unfortunately, this treatment is not particularly useful because the author accepted an exceedingly broad species concept and actually very many distinct and easily recognizable exotic species has simply been lumped with S. apocarpum (Hedw.) Bruch & Schimp. in B., S. & G. In tropical East Africa at least five distinct species have so far been recorded (Kis 1985), but it is very likely that this number will increase with progress in taxonomic study of the genus and floristic exploration of the bryologically undercollected areas

The whole and its parts : why and how to disentangle plant communities and synusiae in vegetation classification

Most plant communities consist of different structural and ecological subsets, ranging from cryptogams to different tree layers. The completeness and approach with which these subsets are sampled have implications for vegetation classification. Non‐vascular plants are often omitted or sometimes treated separately, referring to their assemblages as “synusiae” (e.g. epiphytes on bark, saxicolous species on rocks). The distinction of complete plant communities (phytocoenoses or holocoenoses) from their parts (synusiae or merocoenoses) is crucial to avoid logical problems and inconsistencies of the resulting classification systems. We here describe theoretical differences between the phytocoenosis as a whole and its parts, and outline consequences of this distinction for practise and terminology in vegetation classification. To implement a clearer separation, we call for modifications of the International Code of Phytosociological Nomenclature and the EuroVegChecklist. We believe that these steps will make vegetation classification systems better applicable and raise the recognition of the importance of non‐vascular plants in the vegetation as well as their interplay with vascular plants

The importance of the oil-shale Bings of West Lothian, Scotland, to local and national biodiversity

The oil-shale bings of West Lothian, Scotland, are a group of post-industrial waste sites, unique in Britain and Western Europe. The industrial exploitation of oil-bearing rocks has created a habitat with its own distinctive flora and fauna. The floral diversity of individual sites has been documented as species lists in several studies. A comprehensive list of more than 350 plant species, with supplementary information on animal species, was compiled from an extensive literature review of these studies. From these data it was possible to determine the extent of species variation within and between bings, identify locally and nationally rare species, and thus to determine the importance of the oil-shale bing habitat at a local and national scale. The results will go some way to allay concerns about the loss of local biodiversity, generally throughout the country side, due to changes in agricultural practices and increased urbanisation. Findings from the bings and evidence from other types of derelict land suggest that species are not lost, they have moved to new habitats

Ecology and conservation of bryophytes and lichens on Fagus sylvatica

Environmental factors related to the occurrence of epiphytic bryophytes and lichens were examined in beech (Fagus sylvatica) forests in the Province of Halland, Sweden. Patterns in species composition and species number at different temporal and spatial scales were analyzed with emphasis on species of conservation concern (i.e. red-listed and indicator species). (I) At stand level, the availability of substrate, a high stand age and forest continuity were the most important factors explaining high species number of epiphytes of conservation concern. The difference in species number between stands with and without forest continuity was probably related to the presence of old trees and the time available for species colonization. (II) Within stands, plots containing old trees, at the base of slopes and with low recent forestry impact had the highest species number. At tree level, age, size and moss cover were primary factors in explaining both species number and species composition of all species. Red-listed lichens were associated with damaged beech trees older than 180 years, whereas the few red-listed bryophytes were also recorded on younger stems in dense stands. (III) The vertical distribution of epiphytes, recorded on newly fallen beech stems, could also be related to tree age. Some red-listed lichens were recorded only from above 2 m in height on trees older than 250 years. The presence of any species of conservation concern at 2-5 m height on standing living beech trees correlated positively to moss cover and bark structure, which in turn was dependent on tree age. (IV) The effect of bark and tree characteristics on species occurrence was studied. It was found that the combination of high bark pH, high tree age and damaged stem best explained the number of species of conservation concern. The link between old beech trees and high bark pH was partly explained by a positive effect of tree age on stemflow pH. (V) At microhabitat level, the type of stem damage rot hole was found to positively influence bark pH and the occurrence of species of conservation concern. Old and slow-growing trees with rot holes are, however, often removed from managed beech forests. A spatial separation between managed and retention areas is therefore recommended in shelterwood forestry