Peter H. Raven

Evolution of subalpine and alpine plant groups in New Zealand

Abstract Although some of the plants of alpine and subalpine habitats in New Zealand are derived from ancestors that have been present since Paleogene, or possibly Cretaceous, times, many entered via Australia following the late Pliocene and subsequent elevation of mountains in Malaysia, New Guinea, Australia, and New Zealand. The New Zealand alpine and subalpine habitats only developed in the past few million years, during which they have been profoundly and repeatedly altered by Pleistocene glaciations and finally by man. As these habitats developed in isolation they were colonised mainly by plants derived from Australia, as a result of long-distance dispersal. Westward dispersal, in the face of the prevailing westerlies, is almost ruled out for Australasian plants. In New Zealand, many of them evolved rapidly to produce numerous species in consequence of the processes of adaptive radiation, interspecific hybridisation and recombination, and in many instances self-pollination. These large clusters of sp...

The Origins of Taxonomy.

There are approximately 10 million kinds of olganisms in the world, of which we have described some 15 percent. The rapid growth of the human population will cause most of the remainder to disappear from the earth before they are seen by a taxonomist. These facts suggest a more rigorous application of priorities in systematic biology as well as a careful review of the principles upon which our taxonomic system is based. Folk taxonomies all over the world are shallow hierarchically and comprise a strictly limited number of generic taxa ranging from about 250 to 800 forms applied to plants and a similar number applied to animals. These numbers are consistent, regardless of the richness of the environment in which the particular people live. Very few specific and varietal taxa are recognized in folk taxonomic systems. Until the invention of movable type in the mid-l5th century, written taxonomies were simply records of the folk taxonomies of particular regions. Subsequently, with the possibility for the wide distribution of books, it began to seem worth while to attempt to describe and name all species of plants and animals in the world. By the year 1700, 698 genera of plants were recognized; and by the year 1778, some 1350 genera, including tens of thousands of species. In 1789 de Jussieu interpolated the family as a higher level taxonomic category in an attempt to reduce the number of important units in the system to a memorable number. The family is still the focal point in systems of angiosperm classification at present, several hundred families being recognized. Problems with the taxonomic system stem largely from the fact that it is not designed as an information retrieval device. In folk taxonomies, names are given to organisms and these are used to communicate about the organisms with others who already know the culturally significant properties of the organisms being discussed. In dealing with the vast numbers of organisms that exist, we tend to overemphasize the process of classification and the decisions it involves at the expense of the information about the organisms that we are supposedly accumulating. Frequent changes in names exacerbate the difficulties of the system and render it still less useful for information retrieval. With modern electronic data processing equipment, it has become possible to record information about organisms, to retain this information in a data bank, and to utilize it for various purposes, including the construction of various taxonomic systems. The invention of high-speed electronic data processing equipment is seen as analogous to but more important than the invention of movable type in the history of systematic biology. By using such equipment to its full potentialities, we should be able to achieve a qualitative improvement in our perception of the living world.

Observations of meiotic chromosomes in Gaura (Onagraceae)

Observations of meiotic chromosomes are reported for all 21 species and 3 additional sub species ofGaura (Onagraceae), based upon a study of 647 individuals from 509 naturally occurring populations throughout the range of the genus. The basic chromosome number for the genus isx = 7, and 18 species are diploid withn = 7. Among these, the self-incompatible ones are often highly chromosomally heterozygous, with no homozygous individuals having been found in nature in the perenrennialsGaura lindheimeri andG. villosa, and two-thirds or more of the individuals apparently heterozygous in the following well-sampled species:G. calcicola, G. longiflora, andG. suffulta subsp.suffulta. In contrast, the autogamous species are entirely chromosomally homozygous or nearly so. Two species ofGaura are reported as chromosomal structural heterozygotes, with about 50% pollen abortion:G. biennis andG. triangulata; the translocation systems originated independently of one another. Two of the three polyploid species,G. sinuata andG. drummondii (G. odorata of many authors), are consistently tetraploid (n = 14) and, despite their cytological autotetraploidy, are thought to have originated following interspecific hybridization. They are the only rhizomatous species in the genus and may have had one ancestor in common. The remaining polyploid,G. coccinea, includes populations withn = 7, 14, 21, and 28, as well as evident interploid hybrids and, frequently, supernumerary chromosomes. The relationship among these populations is close and is maintained by frequent hybridization and exchange of genetic material. No other species seems to have participated in their origin, and the association of their chromosomes is consistently that characteristic of autopolyploidy in plants with tetraploid and higher chromosome numbers.