Integration of palaeontological, historical, and geographical data on the extinction of koa-finches

Identifying the root causes of extinction or endangerment requires long chronological records that begin before a population started to decline and extend until its extinction or functional extinction. We present a case study of the koa‐finches, genus Rhodacanthis, an extinct group of Hawaiian honeycreepers that was specialized to feed on green pods and seeds of the koa tree or other leguminous plants. Six island populations of koa‐finches are known; four in the Holocene fossil record and two that survived until the 1890s. We document the palaeoecological context of the fossils and identify constraints on the age span of the specimen record for each population using stratigraphic contexts, associated radiometric determinations, and museum specimen data. We estimate the potential geographical range of koa‐finches at the time of human arrival using two methods: assessment of their historical and palaeo‐habitats, and geographical information system mapping of the pre‐human distribution of the koa plant (Acacia koa) and its sister species, the koai‘a plant (Acacia koaia). After integrating the foregoing data with chronological records and distributional maps of the potential forcing agents of extinction, we conclude that at least two extinctions of island populations were due to ecological change in the lowlands in the prehistorical and perhaps the early historical periods. In the same time frame, the koa‐finch populations on Hawai‘i Island became rare and restricted to upland refugia, making them vulnerable to the upland forest harvesting and degradation that was accelerating in the 1890s. Neither climatic variation nor mosquito‐vectored diseases are likely to have caused the observed extinctions. This study illustrates an approach that can be applied to many other extinct and endangered island species to better understand the causes of high extinction rates in the human era.     

Influence of historical,geographical and environmental variables on understorey composition and richness in Danish forests

Question: What is the relative influence of forest continuity, environmental differences and geographical context on vegetation and species richness in ancient and recent forests? Location: Himmerland and Hornsherred in Denmark. Methods: Lists of forest species from deciduous forests were subjected to CCA with variation partitioning to quantify the relative amount of variation in species composition attributable to historical, present geographical and environmental variables. GLM was used to estimate the importance of the variables to species richness. Results: The importance of temporal forest continuity in one region was negligible but was considerable in the other. The variation in species composition explained by geographical, environmental and historical variables showed little overlap in both regions, particularly at the fine scale. Conclusions: This paper does not support the idea that differences in the flora between ancient and recent forests is mainly caused by environmental differences. Furthermore, species richness seemed unaffected by isolation and forest connectivity.     

Ecological comparisons between Eastern Asia and North America: historical and geographical perspectives

The close floristic affinities between eastern Asia and North America have long been recognized and intensively studied, however, the ecological and biogeographical consequences of such a floristic relationship between these two remotely separated regions has been largely neglected until recently. Quantitative investigations of such relationships could greatly improve our understanding of many global and historical aspects of species diversity, vegetation dynamics, and biogeography, especially with the rapid developments of cladistic methods of phylogenetic reconstruction. All comparisons and predictions will depend on understanding past and present physical and biological processes (i.e. geological history of the continents and the evolutionary history of organisms), as well as human impacts in both regions. Both species level (life history characteristics, distribution, ecological functions) and community level (species composition, structure, endemism) variables should be investigated. Comparisons should be conducted spatially across vegetation zones and temporally through geological episodes. Emphases on the phylogeny and geological history of component taxa by analysing and synthesizing multidisciplinary data would be helpful, especially with regard to the current trends in global climate change. Diversity measured on different scales (i.e. α-, β, and g-diversity) could provide invaluable information about local-regional relationships and their ecological implications in continental or even global biodiversity patterns.     

Male response to historical and geographical variation in bird song

In many species, individuals discriminate among sexual signals of conspecific populations in the contexts of mate choice and male–male competition. Differences in signals among populations (geographical variation) are in part the result of signal evolution within populations (temporal variation). Understanding the relative effect of temporal and geographical signal variation on signal salience may therefore provide insight into the evolution of behavioural discrimination. However, no study, to my knowledge, has compared behavioural response to historical signals with response to current signal variation among populations. Here, I measured the response of male white-crowned sparrows (Zonotrichia leucophrys) to historical songs compared with current songs from their local population, a nearby non-local population and a distant population. Males responded most strongly to current local songs, less, but equally, to historical local and current non-local songs, and least to songs of the distant population. Moreover, response to both temporal and geographical variation in song was proportional to how much songs differed acoustically from current local songs. Signal evolution on an ecological time scale appears to have an effect on signal salience comparable to differences found between current neighbouring populations, supporting the idea that behavioural discrimination among learned signals of conspecific populations can evolve relatively rapidly.     

Laticifers: An historical perspective

This review describes the development of the laticifer concept, with emphasis upon the nonarticulated type, from early observations of plant exudates and “juices” to the presentation of laticifers by Esau (1953). Classical writers and herbalists described practical applications of these substances. With the advent of the microscope early investigators believed that these substances occurred in structures present in most, if not all, plants and, wrongly, equated these structures to the circulatory system in animals. Introduction of the term, latex, into botany derived from its early use as a term for a blood component by physicians, and not for analogy to milk. However, the origin of the terms, laticifer and laticiferous, remains uncertain. Initial studies of laticifers were marked by the controversy of whether they represented intercellular spaces or elongated cells. Confirmation of their cellular character led to the designation of nonarticulated and articulated laticifers. Nonarticulated laticifers were shown to arise during early embryogeny in some plants. The ontogenetic origin of the articulated laticifer was unclear to early workers, but new laticifers were detected to be formed by cambium activity. Nonarticulated laticifers were described to develop by intrusive growth whereby tips of the cell penetrated between adjacent cells. The coenocytic condition of the nonarticulated laticifer resulted from nuclear divisions along the cell positioned in the growth region of the shoot and the subsequent distribution of the daughter nuclei along the length of the cell.     

An ecological study of troop fissions of Japanese monkeys (Macaca fuscata yakui) on Yakushima Island,Japan

Wild, habituated, Japanese monkeys were observed from 1975 to 1979 on Yakushima Island, Southern Japan. The monkey troops had a continuous distribution in a warm temperate forest. Demographic data on local populations was collected. The population density was 33 animals/km². The growth rate of the studied troop was 3.0% per year. A significant correlation between home range areas (R) and troop size (P) was found (r=0.955,p<0.005), using anR-P equation,R=1.84P. One troop split into three troops through two successive fissions. Twenty-one intertroop encounters were observed. Five types of encounters were distinguished. The encounters were apparently territorial defence. Increases in birth rate and socionomic sex ratio after the fissions were prominent. The following four factors had a direct effect upon the dispersion of the troops after fission: (1) dominance relation between the fission troops; (2) social pressure of the neighbors; (3) troop's attachment to its home range; and (4) structure of the environment. The home range of Japanese monkeys is a territory, and territoriality is a population regulating mechanism which serves to reduce competition for food.