Integrating the Rabinowitz rarity framework with a National Plant Inventory in South Korea

Increasingly large presence‐only survey datasets are becoming available for use in conservation assessments. Potentially, these records could be used to determine spatial patterns of plant species rarity and endemism. We test the integration of a large South Korean species record database with Rabinowitz rarity classes. Rabinowitz proposed seven classes of species rarity using three variables: geographic range, habitat specificity, and local population size. We estimated the range size and local abundance of 2,215 plant species from species occurrence records and habitat specificity as the number of landcover types each species’ records were found in. We classified each species into a rarity class or as common, compared species composition by class to national lists, and mapped the spatial pattern of species richness for each rarity class. Species were classed to narrow or wide geographic ranges using 315 km, the average from a range size index of all species (D_max), based on maximum distance between observations. There were four classes each within the narrow and wide range groups, sorted using cutoffs of local abundance and habitat specificity. Nationally listed endangered species only appeared in the narrow‐range classes, while nationally listed endemic species appeared in almost all classes. Species richness in most rarity classes was high in northeastern South Korea especially for species with narrow ranges. Policy implications. Large presence‐only surveys may be able to estimate some classes of rarity better than others, but modification to include estimates of local abundance and habitat types, could greatly increase their utility. Application of the Rabinowitz rarity framework to such surveys can extend their utility beyond species distribution models and can identify areas that need further surveys and for conservation priority. Future studies should be aware of the subjectivity of the rarity classification and that regional scale implementations of the framework may differ.     

Drivers and interrelationships among multiple dimensions of rarity for freshwater fishes

Species can be rare or common in three different dimensions: geographic range size, habitat breadth, and local abundance. Understanding drivers of rarity are not only fundamentally interesting; it is also pertinent for their conservation. We addressed this challenge by analyzing the rarity of 291 native freshwater fishes occurring in ca 3500 independent stream reaches that span a broad environmental gradient across continental USA. Using phylogenetic regression and path analysis, we examined the concordance among the three rarity dimensions, and identified possible mechanisms by which species life‐history, habitat affinities, and biogeography drive variation in rarity. Weak double extinction jeopardies were driven by weakly positive correlations between habitat breadth and local abundance, and between habitat breadth and geographic range size. However, a triple extinction jeopardy was averted as local abundance and range size were not positively linked in our study. This is because large‐river and lacustrine habitat use mediated a trade‐off between local abundance and range size. Large rivers and lacustrine habitats represent important dispersal pathways and refugia that enabled fishes to acquire wide ranges; however, species using these habitats are less abundant overall because they are less adapted to small lotic channels, which comprise the majority of stream habitats in the US. Life‐history traits were key in governing the relationship between abundance and range size as large‐river and lacustrine habitat use were driven by body size, egg size, and parental care. Our analysis contributes novel insights into mechanisms that underlie multiple dimensions of rarity in freshwater fish and informs the prioritization of multiply rare species for conservation.     

Rarity and species/area relationships of vascular plants in deciduous woods, western Norway - applications to nature reserve selection

The Rabinowitz s model of rarity was applied to a vascular plant census list from 60 deciduous woods in western Norway By applying information from distribution maps and plant sociological literature from western Norway it was possible to obtain data on geographical distribution, habitat specificity, and maximum local population size at the regional-scale of western Norway This enabled a comparison between rarity at the local scale and rarity at the regional scale At the local scale rarity was primarily due to narrow geographic distribution At the regional scale, however, the most frequent form of rarity was due to restricted habitat specificity The species/area relationship and the SLOSS effect for the rare species at the regional scale are compared with patterns involving the total species list It is shown that a single large wood supports fewer regional-scale rare species than do combinations of two small woods of equal area The species/area relationship for species with small population sizes at the regional scale has a different slope from the species/area relationship for all species Area is a better predictor of regional-scale rarity than is the number of common species     

Distribution Patterns and Conservation Perspectives of the Endemic Flora of Peloponnese (Greece)

An inventory of the endemic vascular plants of the Peloponnese (395 species and subspecies) has been created based on literature, herbarium and field data. Endemics?? distribution patterns, altitudinal distribution and habitat specificity were investigated. A rarity score for each endemic has been calculated based on its population size, geographic range and habitat specificity. The main mountainous areas of the Peloponnese are largely congruent to the hotspots of endemism. Altitudinal range and niche breadth of the endemics were positively correlated to their range size. The elevational gradient of the endemic species richness showed a hump-shaped pattern, in contrast to the monotonically decreasing pattern of total species richness. Endemic species were found to support boundary theory, while total species richness distribution followed the Rapoport??s elevational rule. The elevational distribution of the average rarity score and the average weighted threat of the endemics resulted in low values for mid-elevation intervals and increased values for low and high altitude areas, indicating that conservation efforts should focus on the two extremes of the elevational gradient. Area prioritization methods were applied using a rarity/complementarity based algorithm with two species weighting schemes. Their results were largely congruent confirming the significance of the main mountainous areas for the conservation of the endemics. Spatial overlap among selected grid cells using the rarity/complementarity analysis and Natura 2000 network was found to be low. Our results revealed the conservation importance of at least one new area located on Kythera Island.     

The importance of rare species: a trait‐based assessment of rare species contributions to functional diversity and possible ecosystem function in tall‐grass prairies

The majority of species in ecosystems are rare, but the ecosystem consequences of losing rare species are poorly known. To understand how rare species may influence ecosystem functioning, this study quantifies the contribution of species based on their relative level of rarity to community functional diversity using a trait‐based approach. Given that rarity can be defined in several different ways, we use four different definitions of rarity: abundance (mean and maximum), geographic range, and habitat specificity. We find that rarer species contribute to functional diversity when rarity is defined by maximum abundance, geographic range, and habitat specificity. However, rarer species are functionally redundant when rarity is defined by mean abundance. Furthermore, when using abundance‐weighted analyses, we find that rare species typically contribute significantly less to functional diversity than common species due to their low abundances. These results suggest that rare species have the potential to play an important role in ecosystem functioning, either by offering novel contributions to functional diversity or via functional redundancy depending on how rare species are defined. Yet, these contributions are likely to be greatest if the abundance of rare species increases due to environmental change. We argue that given the paucity of data on rare species, understanding the contribution of rare species to community functional diversity is an important first step to understanding the potential role of rare species in ecosystem functioning.     

Relationships between geographical range size, body size, local abundance, and habitat breadth in North American suckers and sunfishes

Aim I examine the relationship between geographical range size and three variables (body size, an index of habitat breadth, and an index of local abundance) within a phylogenetic framework in North American species of suckers and sunfishes. Location North America Methods Regressions after independent contrasts of geographical range size, body size, habitat breadth, and local abundance. Results Species with large range sizes tend to be larger-bodied, be more locally abundant, and have higher habitat breadths. Character reconstructions support the prediction that variables associated with rarity (small geographical range size, low local abundance, low niche breadth, and large body size) evolve in unison, although large body size was associated with the opposite traits in these taxa. Gaston & Blackburn (1996a) suggested using visual identification of the lower boundary of the geographical range-body size relationship to identify extinction-prone species; this resulted in thirteen species that are potentially extinction-prone. Main conclusions Similar evolutionary mechanisms appear to operate on body size and other variables related to rarity, even in distantly related taxa.     

The population ecology of rare species

There is no general theory of rarity, although one is sorely needed both to understand population dynamics and to determine conservation priorities. Here we suggest some of the strands that might be woven into such a theory. They include relationships between local abundance, geographic range size and body size of species, and the determinants of minimum viable population sizes. In each of these areas much can still be learnt from the classical 'compare and contrast' approach using assemblages of species from a variety of taxa. Freshwater fish have contributed relatively little to the broad ecological literature in this respect. We perform some tentative analyses for this group of species, and speculate on how they might fit into our current understanding of rarity.     

Growth and reproduction of New Zealand

In New Zealand, as elsewhere, research on rare species has been dominated by autecological studies of individual threatened species. Limitations of this approach are that it involves no comparison with related common species which may have similar traits, and that the minimal sample size prevents generalisation about causes and consequences of rarity. We report on experimentally determined growth and reproductive traits of 10 rare and common Acaena(Rosaceae) species from two taxonomic sections (sect. Ancistrum and sect. Microphyllae). We examined the relationship between rarity or commonness and relative growth rate, mode of vegetative expansion, morphology/presentation of reproductive structures and reproductive allocation. Rarity and commonness were defined according to geographic range size, measured as the number of 10-km grid squares containing at least one record of the species. There were tendencies across both taxonomic sections for species with large range size to have higher relative growth rates and in section Microphyllae, faster lateral expansion. Among section Ancistrum species, common species tended to produce inflorescences for a shorter period and held their capitula higher above the canopy, but other reproductive attributes showed little association with range size. In section Microphyllae all reproductive traits tended to be positively associated with range size. This was mainly due to the single very common species having high fecundity. The lack of strong patterns among our results may reflect insufficient sample size or that the rare species represent different types of rarity.     

Doomed to die? Predicting extinction risk in the true hawks Accipitridae

One of the most important tasks in conservation biology is identifying species at risk from extinction and establishing the most likely factors influencing this risk. Here, we consider an ecologically well-defined, monophyletic group of organisms, the true hawks of the family Accipitridae, which are not only among the most studied, but also contain some of the rarest bird species in the world. We investigate which intrinsic and extrinsic factors, covering morphology, life history and ecology, covary with International Union for the Conservation of Nature and Natural Resources threat status, as well as global population size and geographic range size. By decomposing threat status into population size and range size, we test whether any factors are generally important: we found that species with less habitat specialization, a larger clutch size and more plumage polymorphism were associated with lower extinction risk and larger population and range sizes. Species with special habitat requirements might be less capable of dealing with habitat transformation and fragmentation, while species with small clutch sizes might not be able to reverse population declines. Plumage polymorphism might indicate the size of the species' gene pool and could be a good marker of extinction risk. The analyses also emphasized that no single factor is likely to be sufficient when predicting the threat of extinction.     

Host specificity and geographic range in haematophagous ectoparasites

A negative interspecific correlation between the degree of habitat specialization and the size of a species' geographic range has been documented for several free living groups of organisms, providing support for the niche breadth hypothesis. In contrast, practically nothing is known about the geographic range sizes of parasitic organisms and their determinants. In the context of the niche breadth hypothesis, parasites represent ideal study systems, because of the well documented variation in host specificity among parasite species. Here, we investigated the relationship between host specificity (a measure of niche breadth) and geographic range size among flea species parasitic on small mammals, using data from seven distinct geographical regions. Two measures of host specificity were used: the number of host species used by a flea species, and a measure of the average taxonomic distance between the host species used by a flea; the latter index provides an evolutionary perspective on host specificity. After correcting for phylogenetic influences, and using either of our two measures of host specificity, the degree of host specificity of fleas was negatively correlated with the size of their geographic range in all seven regions studied here, with only one minor exception. Overall, these results provide strong support for the niche breadth hypothesis, although other explanations cannot be ruled out.     

Reproductive features of Celmisia species (Asteraceae) in relation to altitude and geographical range in New Zealand

A range of seed and flower characters was examined in 37 species of the New Zealand genus Celmisia (Asteraceae) to determine whether there were any relationships between reproductive features and the geographic or altitudinal ranges of the species. Using published sources and herbarium material, flower attractiveness to pollinators was measured in terms of capitulum size and ray/disc length ratio. Dispersibility was measured in terms of seed dry weight, seed terminal velocity, pappus/seed length ratio, and scape/leaf length ratio. Altitude (minimum and maximum) and geographic ranges (number of 1^o latitude x 1^o longitude squares occupied) were obtained from published sources. A multivariate principal components analysis using 12 morphological characters revealed the presence of five groups of species differing in capitulum size, seed weight, pappus length, number of pappus bristles, leaf length and scape length. Linear regressions showed that altitude was significantly and negatively related to seed dry weight and capitulum size, and positively to scape/leaf length ratio. Geographic range is negatively related to capitulum size, and positively to ray/disc ratio and altitudinal range. Amongst the seed features measured, seed weight was the best predictor of terminal velocity (an inverse measure of dispersability), but lighter seeds also had a higher pappus/seed length ratio. The frequency distribution of the geographic ranges of the species is highly skewed, with many local species (86% occurring in 15 or fewer one‐degree squares) and very few common ones. Two species (C. gracilenta and C. graminifolia) are notably more common than all the others. A comparison of these species with the others shows that, on average, they have lighter seeds with more bristles, taller scapes and higher ray/disc ratios, but have smaller capitula. The low geographic abundance of the rare species could not readily be attributed to any specific reproductive feature, possibly because of the multiple types of rarity represented within the genus.     

Neither species geographic range size,climatic envelope,nor intraspecific leaf trait variability capture habitat specialization in a hyperdiverse Amazonian forest

Many plant species exhibit strong association with topographic habitats at local scales. However, the historical biogeographic and physiological drivers of habitat specialization are still poorly understood, and there is a need for relatively easy‐to‐measure predictors of species habitat niche breadth. Here, we explore whether species geographic range, climatic envelope, or intraspecific variability in leaf traits is related to the degree of habitat specialization in a hyperdiverse tropical tree community in Amazonian Ecuador. Contrary to our expectations, we find no effect of the size of species geographic ranges, the diversity of climate a species experiences across its range, or intraspecific variability in leaf traits in predicting topographic habitat association in the ~300 most common tropical tree species in a 25‐ha tropical forest plot. In addition, there was no phylogenetic signal to habitat specialization. We conclude that species geographic range size, climatic niche breadth, and intraspecific variability in leaf traits fail to capture the habitat specialization patterns observed in this highly diverse tropical forest.     

Forms of rarity of tree species in the southern Brazilian Atlantic rainforest

The assessment of species rarity considers local abundance (scarce or abundant population), habitat affinity (stenoecious or euryecious species), and geographic distribution (stenotopic or eurytopic species). When analyzed together these variables classify species into eight categories, from common species to those having small populations, unique habitats, and restricted geographic distribution (form 7), as proposed by Rabinowitz in 1981. Based on these categories, it is possible to calculate the frequency of the different forms of rarity of the species present in a given site. The Brazilian Atlantic rainforest is considered a hotspot of the world biodiversity harboring many endemic species, which have restricted geographic distribution. Our objective was to identify the forms of rarity of tree species and their proportions in the southern portion of the Brazilian Atlantic rainforest using Rabinowitz’s forms of rarity. All the seven forms of rarity are present in the 846 tree species we analyzed: 46% eurytopic and 54% stenotopic, 73% euryecious and 27% stenoecious, 76% locally abundant and 24% locally scarce species. Eurytopic, euryecious locally abundant species accounted for 41.1%, whereas 58.9% were somehow rare: 4.5% eurytopic, euryecious locally scarce, 0.2% eurytopic, stenoecious locally abundant, 0.1% eurytopic, stenoecious locally scarce, 19.5% stenotopic, euryecious locally abundant, 8.0% stenotopic, euryecious locally scarce, 15.6% stenotopic, stenoecious locally abundant, and 11.0% stenotopic, stenoecious locally scarce. Considering that the most restrictive forms of rarity precedes extinction, the application of Rabinowitz’s system demonstrated that most tree species of the southern Brazilian Atlantic rainforest are threatened due to their restricted geographic distribution, restriction to a single habitat, reduced local abundance, or even to a combination of these variables.     

Life history tactics of darters (Percidae: Etheostomatiini) and their relationship with body size, reproductive behaviour, latitude and rarity

Patterns of covariation of life history traits of darters in the genus Etheostoma are reviewed. The primary pattern is associated with body size. Large darters grow faster, mature at a larger size, produce bigger clutches, and have longer reproductive and life spans, and shorter spawning seasons, than do small darters. When the effects of size are removed statistically, the dominant secondary pattern matched the r-K continuum from fast-growing, short-lived, primarily semelparous species with many small ova and a high reproductive effort (r-species) to slow-growing, long-lived, iteroparous species with few large ova and a low reproductive effort (K-species). Variation in life history traits is also influenced by reproductive behaviour, latitude, and rarity (as measured by geographic range). There are significant differences in the primary and secondary life history patterns among reproductive guilds. Latitude and rarity are not correlated with these primary and secondary patterns. Instead, they account for variation of tertiary patterns. Rare species may not match the reproductive performance of more common and widely distributed species. Future studies of life history traits in darters should focus on species whose reproductive behaviour differs from that of the species reviewed in this study, and on the demographic characteristics of rare or declining populations.     

昆虫体型及性体型二型性的地理变异

体型是昆虫基本的形态特性,它会影响到昆虫几乎所有的生理和生活史特性。同种昆虫不同地理种群在体型上常表现出明显的渐变,导致这些渐变的环境因素包括温度、湿度、光照、寄主植物、种群密度等,并且多种环境因素也会对昆虫种群内个体体型产生影响。雌雄个体的体型存在差异,称性体型二型性。性体型二型性也显示了地理差异。这些差异形成的途径已经得到详细的分析,其形成机制导致多个假说的提出,这些假说又在多种昆虫中得到验证。本文从同一种昆虫不同种群间、同一种群内、雌雄虫个体间3个水平,对种内昆虫体型变异的方式,影响昆虫种群间体型变异和种群内昆虫体型的变异的环境因素,以及昆虫性体型二型性及其地理变异的现象等方面的研究进行了综述,并对未来的相关研究提供了建议。     

Long-term differences in extinction risk among the seven forms of rarity

Rarity is widely used to predict the vulnerability of species to extinction. Species can be rare in markedly different ways, but the relative impacts of these different forms of rarity on extinction risk are poorly known and cannot be determined through observations of species that are not yet extinct. The fossil record provides a valuable archive with which we can directly determine which aspects of rarity lead to the greatest risk. Previous palaeontological analyses confirm that rarity is associated with extinction risk, but the relative contributions of different types of rarity to extinction risk remain unknown because their impacts have never been examined simultaneously. Here, we analyse a global database of fossil marine animals spanning the past 500 million years, examining differential extinction with respect to multiple rarity types within each geological stage. We observe systematic differences in extinction risk over time among marine genera classified according to their rarity. Geographic range played a primary role in determining extinction, and habitat breadth a secondary role, whereas local abundance had little effect. These results suggest that current reductions in geographic range size will lead to pronounced increases in long-term extinction risk even if local populations are relatively large at present.     

Better common than rare? Effects of low reproductive success,scarce pollinator visits and interspecific gene flow in threatened and common species of Tibouchina (Melastomataceae)

The reasons for plant rarity have been the focus of many studies, especially because rare species are more prone to extinction than common species. Under the same habitat conditions, rare plants are expected to attract fewer flower visitors and to show some limitation in their reproductive success. Here, using one of the most emblematic Neotropical plant genus (Tibouchina) we tested whether narrow endemic and threatened species in Ecuador have a lower reproductive success or are visited by fewer pollinators than common species, in 13 populations monitored from 2011 to 2013. We also assessed whether interspecific gene flow could be considered a threat to the rare species. However, contrary to expectations, we found that few pollinators visited the flowers, independently of species rarity. Natural outcross pollinations were always very low in all small‐size populations, leading to high levels of pollen limitation. Interspecific crossing experiments also revealed weak reproductive barriers in some species. This study reveals that both narrow and common species of Tibouchina have similar reproductive and pollinator patterns in Ecuador and, therefore, other causes of the rarity of these species should be considered.     

The value of structuring rarity: the seven types and links to reproductive ecology

Since 1981, 365 papers have cited a rarity matrix organized along three axes: geographic range (GR) (large vs. small), habitat specificity (HS) (specialist vs. generalist), and local abundance (LA) (dense vs. sparse). In the wider ecology literature, research on the association between plant species distributions and life history traits has mainly focused on a single axis such as GR. However, the internal structure of species ranges is widely recognized as important. In order to determine if identifying different types of rarity leads to alternative conclusions regarding the causes and consequences of rarity, we created a dataset linking the seven types of rarity matrix and to reproductive ecology traits. We found associations between the axes and these traits in a dataset of 101 rare plant species culled from 27 papers. Significant traits included mating system and seed dispersal mechanism. Species with small GR are more likely to have ballistic or wind dispersal than biotically-mediated dispersal (abiotic:biotic ratio 3:1). Habitat specialist species with small GRs are more likely to have outcrossing mating systems compared to habitat specialists of large GR (16:1). These results show that, within rare species, the structure of rarity is important (e.g. habitat specialization is different from small GR) and should be identified when determining basic mechanisms of plant distribution and abundance.     

Patterns and correlates of plant diversity differ between common and rare species in a neotropical dry forest

Determining which factors affect species richness is important for conservation theory and practice. However, richness of common and rare species may be affected by different factors. We use an extensive inventory of woody plants from a tropical dry forest landscape in Yucatan, Mexico to assess the unique effects of environmental variables, spatial dependence of sampling sites, forest stand age and the combined effect of all groups of variables on species richness of woody plants with different levels of rarity (common, intermediate, rare, very rare)—according to their abundance, habitat specificity and spatial distribution range in the landscape. Analyzing separately common species and those with different levels of rarity uncovered contrasting patterns and correlates of species richness that were not apparent when focusing on all woody plants. In particular, richness of common and intermediate species was influenced mainly by environmental factors, whereas richness of very rare species was affected mostly by the unique effect of spatial dependence of sampling sites, suggesting a main role of environmental filtering and dispersal limitation, respectively. However, common and very rare species also responded inversely to some landscape metrics, revealing contrasting environmental preferences of these groups of species. These contrasting results suggest different underlying mechanisms and the need for very different conservation strategies. Therefore, basic and applied research on tropical forest biodiversity should consider separately species with different levels of rarity, focusing on which factors control variation in each level, and paying special attention to very rare species, generally the most specious and vulnerable to local extinction.