XXV.—The Prothallus of Tmesipteris Tannensis

1917 ◽  
Vol 51 (3) ◽  
pp. 785-794 ◽  
Author(s):  
A. Anstruther Lawson

The Psilotaceæ constitute one of the most interesting of existing Pteridophyte groups. This interest is mainly due to their phylogenetic isolation. They are perhaps the most isolated of existing types—showing no close affinity to other Pteridophytes. They are very highly specialised in their anatomy, habit, and habitat, and limited to a comparatively narrow geographical distribution. They include two probably monotypic genera—Tmesipteris and Psilotum—which are closely related. Although both genera are limited to the tropics and sub-tropics, Psilotum has a much wider distribution than Tmesipteris. The latter is confined to the South Sea Islands, Australia, New Zealand, and parts of Polynesia. Up till recent years they have been classed with the Lycopodiales, but this has been more a matter of convenience than an indication of close relationship, and has only served as a temporary classification until more knowledge has been obtained regarding them. The peculiar nature of these plants, as shown in their structure and in their habitat, suggests that they are highly specialised remnants of a much larger group which has practically become extinct. Recent inquiry into the structure of the sporophyte of both plants has made this much more than a suggestion. As a result of the careful investigations of Scott (1908), Boodle (1904), Bower (1894-1908), Ford (1904), and others, there has been a marked tendency to remove the Psilotaceæ from their temporary position among the Lycopodiales and associate them with the extinct Sphenophyllales. Scott (p. 631) states that it seems best to regard the Psilotaceæ as forming a class of their own, the Psilotales, under the main division Sphenopsida—their closest affinity under this class being the Sphenophyllales. This probable affinity of the Psilotaceæ to such an ancient and long extinct race as the Sphenophylls, and the great uncertainty of their relationship to other existing types, have awakened a great interest in these two specialised and isolated genera. When, in addition to this, we consider that the Psilotaceæ is the only group of Pteridophytes in which the gametophyte generation and embryo are not yet definitely known, our interest in these plants becomes twofold, and any new information throwing additional light on their life-histories will be welcomed.

Author(s):  
A. Sivanesan

Abstract A description is provided for Diplocarpon maculatum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Amelanchier, Aronia, Crataegus, Cydonia, Eriobotrya, Heteromeles, Malus, Mespilus, Photinia, Pyracantha, Pyrus, Raphiolepis, Sorbus. DISEASE: Entomosporium leaf blight or Fabraea scald. GEOGRAPHICAL DISTRIBUTION: Generally throughout the temperate zones and extending into the tropics in Central America and highlands of Kenya. North America (Canada, USA, Mexico), Central American states, South America (Argentina, Brazil, Chile, Colombia, Uruguay), Europe, Africa (Morocco, South Africa, Rhodesia, Mozambique, Madagascar, Kenya), Asia (Afghanistan, India, Israel, Japan, Turkey, USSR), Australia and New Zealand (CMI Map 327, ed. 2, 1968). TRANSMISSION: By splash dispersed conidia; ascospores appear to be of minor importance.


1890 ◽  
Vol 35 (2) ◽  
pp. 489-525 ◽  
Author(s):  
George Stewardson Brady

Excepting the few species noticed in the Report on the Ostracoda of the “Challenger” Expedition, scarcely anything, so far as I know, has been published respecting the Ostracoda of the South Sea Islands. Prof. G. M. Thomson has indeed published in the Transactions of the New Zealand Institute (1878), a paper on Crustacea, which includes a few marine and fresh-water Ostracoda of New Zealand; and the Rev. R. L. King, in the Proceedings of the Royal Society of Van Diemen's Land (1855), described numerous species of Entomostraca, amongst which were several fresh-water, but no marine, Ostracoda. Dr Baird also published a species of Cypridina from New Zealand. I have myself contributed to the Proceedings of the Zoological Society of London (1886) a paper on Entomostraca collected in South Australia, chiefly by Professor Ralph Tate of Adelaide, including a considerable number of fresh-water Ostracoda; and in a French publication (Les Fonds de la Mer), edited by the Marquis de Folin, there are likewise, by myself, descriptions of a few species taken at Nouméa, New Caledonia. There are also, in a paper of mine published in the Transactions of the Zoological Society (1865), notes of a few Australian marine species. This, I think, represents the sum of our present knowledge respecting the Ostracoda of these regions.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Javier Fernández-López ◽  
M. Teresa Telleria ◽  
Margarita Dueñas ◽  
Mara Laguna-Castro ◽  
Klaus Schliep ◽  
...  

AbstractThe use of different sources of evidence has been recommended in order to conduct species delimitation analyses to solve taxonomic issues. In this study, we use a maximum likelihood framework to combine morphological and molecular traits to study the case of Xylodon australis (Hymenochaetales, Basidiomycota) using the locate.yeti function from the phytools R package. Xylodon australis has been considered a single species distributed across Australia, New Zealand and Patagonia. Multi-locus phylogenetic analyses were conducted to unmask the actual diversity under X. australis as well as the kinship relations respect their relatives. To assess the taxonomic position of each clade, locate.yeti function was used to locate in a molecular phylogeny the X. australis type material for which no molecular data was available using morphological continuous traits. Two different species were distinguished under the X. australis name, one from Australia–New Zealand and other from Patagonia. In addition, a close relationship with Xylodon lenis, a species from the South East of Asia, was confirmed for the Patagonian clade. We discuss the implications of our results for the biogeographical history of this genus and we evaluate the potential of this method to be used with historical collections for which molecular data is not available.


2021 ◽  
Vol 13 (8) ◽  
Author(s):  
Matthew Campbell ◽  
Julian Lilkendey ◽  
Malcolm Reid ◽  
Richard Walter ◽  
Kavindra Wijenayake ◽  
...  

2015 ◽  
Vol 43 (2) ◽  
pp. 317-341
Author(s):  
Hugh Roberts

“I have read your poems – you can do anything” wrote Robert Browning to his close friend Alfred Domett on May 22, 1842, shortly after the latter had emigrated to New Zealand (Browning, Domett and Arnould 35). If this was in part friendly overpraise of Domett's verse, it was also a prognostication as to the effect of emigration. The idea (which also underlies Browning's poetic treatment of Domett's departure in the figure of Waring who “gave us all the slip”) was that “partial retirement and stopping the ears against the noise outside” would open up the possibility of something startlingly new: the little I, or anybody, can do as it is, comes of them going to New Zealand. . . . What I meant to say was – that only in your present condition of life, so far as I can see, is there any chance of your being able to find out . . . (sic) what is wanted, and how to supply the want when you precisely find it (35).


1960 ◽  
Vol 8 (3) ◽  
pp. 256 ◽  
Author(s):  
W Hartley ◽  
C Slater

In further studies of grass distribution, maps are presented showing the world distribution of the Eragrosteae (sensu str.) and of the subfamily Eragrostoideae within which it is included. Both taxa show centres of high relative specific differentiation in inland Australia and in South West Africa, but in addition, the subfamily has centres of differentiation in the Sahara rekion, northern Mexico, and north-western India. The centres of differentiation are all in regions of hot, arid climate near the tropics of Cancer and Capricorn. The close relationship between climate and distribution is most apparent in the case of the subfamily Eragrostoideae, species of which are relatively abundant in the grass flora of all arid regions with high winter temperatures and summer or non-seasonal rainfall incidence. The distributions of most of the other tribes and subtribes which have been included in the Eragrostoideae show a similar relationship to climate. Some apparent exceptions to this are discussed, and it is shown that the geographical evidence supports conclusions from recent cytotaxonomic and anatomical studies that the taxa concerned should be removed from the subfamily. The very wide distribution of the subfamily and of its constituent taxa, as well as the close relationship between the distribution pattern and climate, suggests that the subfamily is a very old one. Geographical and taxonomic evidence indicates that it may have originated in tropical or subtropical Africa at least as early as the Oligocene.


1946 ◽  
Vol 36 (3) ◽  
pp. 409 ◽  
Author(s):  
John Wesley Coulter
Keyword(s):  

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