Ecological Predictors of Extinction Risk in the Flora of Lowland England, UK

We used historical and contemporary records to determine the scale of plant extinction in Bedfordshire and Northamptonshire, and to assess whether extinct species share a range of ecological and phytogeographical traits. Since 1700 both counties have lost 94 species (11% of their native floras) with the rate of extinction increasing from 3.8 to 4.8 species per decade in the 19th century to 6–8 species per decade after 1950. The most important predictors of extinction risk were English range size and traits associated with habitat specialisation and competitive ability: poor competitors (i.e. short stress-tolerators) associated with open habitats with very low or high pH and soil moisture (e.g. lowland bogs, dwarf-shrub heath and acid and calcareous grassland) were much more likely to have become extinct in the study region than would have been expected by chance alone. Many of these species have very localised distributions and/or occur at the northern, southern or eastern edges of their range in southern England (i.e. Northern and Oceanic). In contrast, there was no clear or significant relationship between extinction and dispersal ability or reproductive mode. These findings, which parallel national trends, indicate that habitat loss and eutrophication have been the main causes of population extinction in lowland England over the last 300 years. However, more fine-scaled studies are required to assess whether ‘low-level’ stresses, such as habitat fragmentation, climate change and atmospheric pollution, are having additional impacts on populations already severely depleted by habitat loss, as well as to quantify changes in the abundance of more widespread species which are known to have declined over the same period.     

Comparison of living-tree and subfossil ringwidths with summer temperatures from 18, 19 and 20 centuries in Northern Finland

This work seeks to analyse the importance of summer-temperatures an the tree-ring growth of Scots pine (Pinus sylvestris L.) during the past three centuries. Three living-tree chronologies, subfossil pine chronology and one composite tree-ring chronology were constructed from latitudinal and altitudinal forest-limits of pine in northern Finland and compared with meteorological data comes from three localities. These data include early instrumental temperature observations from 18^th and 19^th centuries. The modern meteorological data covers the period from 1860 to present. Response functions were derived by means of Pearson correlations using five subperiods as follows: 1738–1748, 1802–1822, 1825–1835, 1861–1926 and 1927–1992. It was demonstrated that the correlations between ringwidths and mid-summer (July) temperatures did not vary significantly as a function of time. Early(June) and late-summer (August) mean temperatures were secondary in relation to mid-summer temperatures in controlling the radial growth. Early-summer temperatures governed pine radial growth most clearly during the 19^th century, whereas late-summer temperatures had strongest influence an ring-widths during the 18^th century and later part of the 20^th century. There was no clear signature of temporally reduced sensitivity of Scots pine ring-widths to mid-summer temperatures over the periods of early meteorological observations. Subfossil pine chronology, constructed using pines recovered from small Jakes along the forest-limit zone, showed a consistent pattern of response to summer-temperatures in relation to living-tree chronologies.     

Seed mass of Indiana Dune genera and families: Taxonomic and ecological correlates

Summary Several surveys have documented an association among species between habitat type and seed mass, suggesting that habitat attributes impose a direct selective force on seed mass. Previous comparative surveys, however, have not controlled for the statistical effects of shared phylogenetic history (at the genus or family level) and life form when evaluating the relationship between habitat and seed mass. This study of the Indiana Dunes angiosperm flora provides statistical control of genus and family membership by: (i) partitioning out the statistical effect of genus membership prior to measuring the effect of habitat on seed mass, and (ii) seeking an association between habitat and seed mass within eight genera (206 species) and ten families (366 species). To measure the associations between ecological factors, taxonomic membership and seed mass, I examined life form, phenological schedules and seed mass among species in 8 genera distributed among 13 habitat types (assigned to 1 of 4 categories of inferred water and light availability). One-way ANOVAS indicated that genus, life form, habitat, water/light category, the onset of flowering and the duration of flowering accounted for 71%, 51%, 10%, 4%, 14% and 14% of the variance in seed mass, respectively. However, multi-factor ANOVAS measured the variance in seed mass accounted for by each variable independently of the others: only genus explained a significant proportion (11%). Genus membership is strongly associated with the other ecological factors, accounting for the difference between one-way and multi-factor ANOVAS. Within the ecologically widespread genera and families of this study, there was no significant association between water/light category and seed mass, even though this association can be detected across taxa. Among congeners and confamilials, interspecific variation in seed mass (measured as the coefficient of variation) was as high within habitat types as among them, suggesting that habitats do not provide upper limits to the range of seed mass exhibited by the species within them. A previous study of 648 Indiana Dune species showed that species segregate among habitats on the basis of seed size; large-seeded species tend to occupy closed habitats and small-seeded species tend to inhabit open habitats. This segregation creates the ecologically meaningful observation that low-light habitats support larger-seeded species than high-light habitats, even though this pattern cannot be detected independently of taxonomic membership. Generalist taxa may occupy a wide range of habitats for reasons other than their seed size. If this is a common feature of ecological generalists, it may not be possible to detect an association between habitat and seed size independently of taxonomic membership.     

Human transformations of the Wadden Sea ecosystem through time: a synthesis

Todays Wadden Sea is a heavily human-altered ecosystem. Shaped by natural forces since its origin 7,500 years ago, humans gradually gained dominance in influencing ecosystem structure and functioning. Here, we reconstruct the timeline of human impacts and the history of ecological changes in the Wadden Sea. We then discuss the ecosystem and societal consequences of observed changes, and conclude with management implications. Human influences have intensified and multiplied over time. Large-scale habitat transformation over the last 1,000 years has eliminated diverse terrestrial, freshwater, brackish and marine habitats. Intensive exploitation of everything from oysters to whales has depleted most large predators and habitat-building species since medieval times. In the twentieth century, pollution, eutrophication, species invasions and, presumably, climate change have had marked impacts on the Wadden Sea flora and fauna. Yet habitat loss and overexploitation were the two main causes for the extinction or severe depletion of 144 species (~20% of total macrobiota). The loss of biodiversity, large predators, special habitats, filter and storage capacity, and degradation in water quality have led to a simplification and homogenisation of the food web structure and ecosystem functioning that has affected the Wadden Sea ecosystem and coastal societies alike. Recent conservation efforts have reversed some negative trends by enabling some birds and mammals to recover and by creating new economic options for society. The Wadden Sea history provides a unique long-term perspective on ecological change, new objectives for conservation, restoration and management, and an ecological baseline that allows us to envision a rich, productive and diverse Wadden Sea ecosystem and coastal society.     

生态恢复方式对喀斯特生境苔藓植物物种组成的影响

为探究生态恢复方式对苔藓植物的影响，研究了自然弃耕和退耕还林等生态恢复方式对重庆市中梁山喀斯特地区不同生境类型下苔藓植物物种组成特征的影响。结果表明，研究区有苔藓植物15科26属41种，其中藓类39种，苔类2种，美灰藓(Eurohypnum leptothollum)为主要优势物种；研究区石生藓类植物占比较大，生活型以平铺型和丛集型为主，各生境物种多样性及相似性指数整体偏低，但相比弃耕杂草地、灌木林和经济型林地，竹林和马尾松林中苔藓植物具有更高的物种多样性；冗余分析表明，郁闭度和光照强度是影响苔藓植物分布的关键环境因子，乔木林为苔藓植物的生长提供了更适宜的生境。因此，相比于自然恢复和经济性林地等恢复方式，退耕还林是喀斯特退化生境更为理想的生态恢复方式。     

浙江景宁畲族自治县石松类和蕨类植物区系研究

在野外调查的基础上,初步探讨了景宁畲族自治县石松类和蕨类植物的区系特征、地理分布、生态环境以及与邻近地区的关系和物种濒危状况。结果表明,景宁石松类和蕨类共有296种7变种和1杂交种,隶属于29科83属,其中包括7个浙江省新记录种;地理分布以热带性质的科属占优势,种类以温带性质为主,本区属于亚热带与温带物种的融汇地带;与邻近省份和地区相比,景宁石松类和蕨类区系与江西省、福建省、宁波市和温州市的关系密切,与温州的区系最紧密,与安徽的区系较疏远;景宁石松类和蕨类生态类型大致可分为六类:暖性针叶林生境、常绿阔叶林阴湿生境、毛竹林暖湿生境、温性松杉柏冷湿生境、灌丛及村旁路边干旱生境和溪流、农田、沼泽湿地生境,其中常绿阔叶林阴湿生境下物种最丰富;景宁分布着在浙江范围内受威胁的蕨类46种,其中濒危(EN)有11种,易危(VU)有35种,国家和浙江省保护蕨类4种。     

Species turnover on a protected subtropical barrier island: a long-term study

Abstract. The commercial development that threatens the biodiversity of coastal habitats is particularly severe along the sandy shores of subtropical Florida. The objective of our study was to test the applicability of the equilibrium theory of island biogeography to Cayo-Costa Island, the largest protected barrier island remaining in peninsular Florida. Our null hypothesis was that there would be no change in the number and composition of native vascular plant species on Cayo-Costa 15 years after the first inventory of the island's flora. Our reinventory documents a total of 230 native species in 1990–92 compared to 255 native species in 1975–77. Immigrants were represented by twenty-eight new species, while extinctions totalled fifty-three species. These results indicate a turnover rate of approximately 2.7 species yr^-1 with an extinction rate of 3.5 species yr^-1 and an immigration rate of 1.9 species yr^-1. The net loss of 1.6 species yr^-1 suggests a non-equilibrium condition that is not readily explained by changes in habitat diversity associated with the documented patterns of shoreline erosion and deposition. Cayo-Costa's net loss of twenty-five native species (including one tree species and four shrub species) was localized mainly in those habitats where there had been a significant increase in the relative abundance of the naturalized weedy exotic species Schinus terebinthifolius and Casuarina equisetifolia . We conclude that the spread of naturalized weedy species limits the applicability of the equilibrium theory of island biogeography to species-rich subtropical barrier islands, even in cases where the islands are protected from human disturbance.     

Seasonal biomass and diversity of estuarine fishes coupled with tropical habitat heterogeneity (southern Gulf of Mexico)

Nekton dynamics were studied in two contrasting habitats in Terminos Lagoon, Mexico. Over an annual cycle, a total of 83 fish species used the high-salinity fringing mangrove/ Thalassia testudinum habitat and biomass ranged from 0.43 to 3.43 g m⁻². The highest biomass occurred during the dry season when aquatic primary production was highest (i.e. 333 g C m⁻² year⁻¹). By contrast, 65 species used the freshwater and low-salinity riverine mangrove/Crassostrea virginica/Vallisneria habitat and biomass ranged from 0.57 to 1.48 g m⁻² with the highest biomass occurring during the wet season, the time of highest primary production in this habitat (i.e. 219 g C m⁻² year⁻¹). The high- and low-salinity habitats serve as ecological bridges between freshwater areas and the sea. Fish life histories have evolved to utilize these habitats for spawning, feeding and nursery grounds in a manner which generally leads to the use of different habitats during the periods of highest primary productivity.     

On choice of substrate and habitat in brachionid rotifers

Information on the distribution of 28 rotifers of the family Brachionidae from diverse waters in south and central Sweden was analyzed to reveal their relationships to substrate and habitat. Some brachionids are preferably planktic, others periphytic and/or benthic. Some non-planktic habitats are utilized more than others, but there is no evidence of a chemical attraction from any substrate. Instead, some substrates seem to be avoided, possibly depending on a poorer flora of periphytic algae. Besides substrate type, the following factors are found to be important for creating separate ecological niches in the brachionid family: temperature, oxygen content, trophic degree, chemical environment, food choice and sensitivity to predation. It is possible to delineate separate ecological niches for all brachionid rotifers, implying that Hutchinson's ideas about the plankton paradox are contradicted. Some species are specialists, other are generalists, the latter being characterized by a great morphological variation. The species are adapted in different ways to their preferential habitats, as regards foot, egg-carrying, protrusions and other lorical structures etc. Longer spines, for instance, are generally found in more transparent water, being a supposed protection against visual predators.     

Evolutionary dynamics of habitat use

I examine the evolution of alternate genotypes that use two habitats that differ in vegetative cover, focusing on the interplay between ecological dynamics of the community and changes in selective advantage. Facultative habitat choice can stabilize a predator population that would cycle if isolated in the more open habitat. This has important implications for the evolution of habitat use strategies. Local stability arising from facultative habitat use allows any number of behavioural genotypes to co-exist: selective use of the open habitat, selective use of the dense habitat, opportunistic use of both habitats in proportion to availability, and facultative switching between habitats to maximize energy gain. Co-existence occurs because the fitness landscape is flat at the ecological equilibrium imposed by the facultative genotype. In contrast, ecological instability favours the evolution of genotypes with behavioural flexibility to avoid being in the wrong place at the wrong time or selective exploitation of one of the habitats. Uncertain information about habitat quality erodes the adaptive advantage of otherwise optimal behaviours, favouring a bet-hedging behavioural strategy synonymous with partial habitat preferences. These results suggest that ecological dynamics could have a strong influence on behavioural heterogeneity within forager populations and that a mixed ESS for habitat use should predominate.