Fern endemism and its correlates: contribution from an elevational transect in Costa Rica

We studied the distribution patterns of endemic ferns along an elevational gradient of 3400 m in Costa Rica, Central America. We related the endemism patterns of the whole species set and separated for life forms and microhabitats according to topography and environmental factors. Fern species were surveyed in 156 plots each with an area of 400 m², with up to five plots at every elevational step of 100 m. Global range size for every species was compiled from literature data, and species restricted to the mountain range from Costa Rica and adjacent western Panama were defined as endemic (24.5% of all species recorded). We found patterns of endemism rates mostly peaking at mid-elevation, but when separated for different life forms and microhabitats, some deviations from the overall pattern emerged. High constant humidity and reduced surface area were closely related to high levels of endemism. High humidity is discussed as a general predictor for high endemism rates in concert with highest overall richness. Restricted area of elevational belts, indicating a fragmented habitat, leads to a higher degree of population isolation and thus species differentiation. However, both interpretations were not fully supported by our data. Most importantly, endemism rates were fairly low on mountain tops that have the smallest available area in a topographically highly fragmented setting. In contrast, endemic species were more common than widespread species at the highest elevations. History and climatic shifts are assumed to play a role in this respect.     

A preliminary assessment of congruence between biodiversity patterns in Afrotropical forest birds and forest mammals

Burgess, N., de Klerk, H., Fjeldsá, J., Crowe, T. & Rahbek, R. 2000. A preliminary assessment of congruence between biodiversity patterns in Afrotropical forest birds and forest mammals. Ostrich 71 (1 & 2): 286–291.

Databases compiled for forest birds and forest mammals in the Afrotropics were tested for congruence of overall patterns and hotspots of species richness and endemism. We also looked at how well a near-minimum set of priority areas for one taxon catered for the second taxon. Overall species richness and richness hotspots of forest birds were significantly correlated with those of forest mammals, as was the case for overall endemism. Endemism hotspots for forest birds and mammals were not significantly correlated. The near-minimum set for forest birds represented 136 (76.5%) forest mammal species. The near-minimum set for forest mammals represented 350 (93.62%) forest bird species. However, to represent all forest mammals three times each, 51 grids were needed in addition to the 78 chosen as a near-minimum set for forest birds, and to represent all forest birds three times each, 43 more grids were needed in addition to the 80 selected for forest mammals. There is some congruence between the patterns of richness, endemism and near-minimum sets for forest birds and mammals in the Afrotropics, but the one taxon does not provide the ideal conservation solution for the other. Further refinement of the databases used in this paper would allow for more rigorous testing of congruence between these two groups.     

Elevation gradients of diversity for rodents and bats in Oaxaca, Mexico

1  This study documents patterns of rodent and bat diversity related to abiotic and biotic factors along elevational gradients in the Sierra Mazateca (640–2600 m a.s.l.) and Sierra Mixteca (700–3000 m a.s.l.) in Oaxaca, Mexico.
2  The two transects share similar faunas: 17 and 23 rodent species were captured in the sierras Mazateca and Mixteca, respectively, 14 of which occurred on both transects. Rodent species richness was similar in the wet season and the dry season along both transects. Rodent species richness peaked at 1025–1050 m in tropical semi-deciduous forest on both transects. Endemic species were restricted to high-elevation habitats.
3  Sixteen and 17 bat species were captured in the sierras Mazateca and Mixteca, respectively; 11 occurred on both transects. Bat species richness was higher in the wet season than in the dry season in the Sierra Mazateca. Bat species richness peaked at 1850 m in pine–oak forest in the Sierra Mazateca, and at 750 m and 1050 m in tropical semi-deciduous forest in the Sierra Mixteca, decreasing abruptly at higher elevations on both transects.
4  Patterns of trophic diversity of rodents and bats coincided with those of species richness on each transect. Species richness increased with increasing habitat diversity; increased with increasing rainfall and productivity; increased with increasing resource diversity; and increased in areas with high rates of speciation (rodents only).
5  The need for conservation action in Oaxaca is urgent and proponents should promote establishment of protected areas linking lowland habitats with high species richness to high-elevation habitats harbouring large numbers of endemic forms.     

Species richness and rarity in European rodents

The presence or absence of 77 rodent species was scored within 427 squares of 100×100 miles. The grid encompassed the entirety of Europe west of the Urals and north of the Caucasus, but excluded all offshore islands. Rodent distributional ranges varied between 26 000 and 22 670 000 km². Very large ranges were uncommon and 53% of species had ranges covering <20% of the study area. Range size showed no correlation with body size, nor did it depend on taxonomic provenance. However, saltatorial rodents appeared to have the largest median ranges and fossorial species the smallest. Species densities varied between 4 and 26 species/grid square, with the highest densities coinciding broadly with the steppe–deciduous forest ecotone. The degree of endemism showed a different geographic pattern from that of species density, with the highest values at lower latitudes. Forty-nine squares (11% of Europe's surface) identified as species richness and endemism "hot spots" contained >80% of genera and species, their largest contiguous coincidence being in the southern Balkans, the Carpathian Basin, southern Ukraine and cis-Caucasia.     

Contrasting patterns of elevational zonation for birds and mammals in the Andes of southeastern Peru

Abstract. To determine the generality of avian diversity patterns, we investigated patterns of elevational zonation shown by birds and mammals along the eastern slope of the Andes Mountains in southeastern Peru. The strong environmental gradient sampled, entirely within Peru's Manu National Park and Biosphere Reserve, supports highly diverse faunas. Elevational distributions of 901 bird species, 129 bat species, and twenty-eight species of native mice exhibit contrasting patterns in species richness, species composition, and species turnover. Birds and bats showed smooth declines of species richness with elevation, whereas the richness of mouse assemblages was unrelated to elevation. For all three groups, the greatest differences were between lowland and highland faunas, although cutoff points for this contrast varied among groups (≈ 500 m for birds, 750 m for bats, and 1000 m for mice). Differences in composition also separated bird and bat faunas on either side of c. 1400 m (the boundary between montance forest and cloud forest); for mice, this faunal transition may take place nearer to 2000 m. Bird and bat faunas lacked the more discrete zonations suggested for mouse assemblages, as indicated by elevational range profiles and nested subset analyses. Distinct highland assemblages are apparent in two-dimensional histograms of range limits of birds and mice, but not for bats. Highland bat species occupy broader elevational ranges than lowland bat species, but for both birds and mice, species at intermediate elevations had the broadest amplitudes. Finally, clumping of range maxima and minima along the gradient identified zones of pronounced species turnover in each group, but these were generally not strongly associated with the locations of ecotones. Differences in zonation of these groups appear to reflect their different biological attributes and phylogenetic histories. Such differences obviously complicate discussions of ‘general’ diversity patterns, and limit the usefulness of birds to forecast or predict diversity patterns in other more poorly known groups—other groups may show elevated diversity and endemism in areas where avian diversity patterns appear unremarkable. The pronounced contrasts between bats and mice, and the generally intermediate character of avian patterns, suggest that future analyses might profitably partition birds into finer, more homogeneous groups of historically and/or ecologically similar species. Group differences in zonation may ultimately prove explicable with information on both species-abundance patterns and resource distributions.     

Understorey plant species richness and composition in metropolitan forest archipelagos: effects of forest size, adjacent land use and distance to the edge

Aim To address the relative role of adjacent land use, distance to forest edge, forest size and their interactions on understorey plant species richness and composition in perimetropolitan forests. Location The metropolitan area of Barcelona, north‐eastern Spain. Methods Twenty sampling sites were distributed in two forest size‐categories: small forest patches (8–90 ha) and large forest areas (> 18,000 ha). For each forest‐size category, five sites were placed adjacent to crops and five sites adjacent to urban areas. Vascular plant species were recorded and human frequentation was scored visually in 210 10 × 10 m plots placed at 10, 50 and 100 m from the forest edge, and additionally at 500 m in large forest areas. Plant species were grouped according to their ecology and rarity categories. A nonmetric multidimensional scaling (NMS) ordination was carried out to detect patterns of variation in species assemblage, and to explore the relationships between these patterns and the richness of the species groups and the studied factors. Factorial anovas were used to test the significance of the studied factors on the richness of species groups. Relationships between human frequentation and the studied variables were assessed through contingency tables. Results Forest‐size category was the main factor affecting synanthropic species (i.e. those thriving in man‐made or man‐disturbed habitats). Synanthropic species richness decreased with increasing distance from the forest edge and, when forests were adjacent to crops, it was higher in small forest patches than in large forest areas. Richness of rare forest species was lower in small forest patches than in large forest areas when forests were adjacent to urban areas. Richness of common forest species and of all forest species together were higher close to the forest edge than far from it when forests were adjacent to urban areas. Forests adjacent to urban areas were more likely to experience high human frequentation, particularly in those plots nearest to the forest edge. Main conclusions Forest‐size category and adjacent land use were the most important factors determining species richness and composition. The preservation of large forests adjacent to crops in peri‐urban areas is recommended, because they are less frequented by humans, are better buffered against the percolation of nonforest species and could favour the persistence of rare forest species.     

Patterns of plant diversity in Africa south of the Sahara and their implications for conservation management

Plant species richness and range-size rarity in Africa south of the Sahara is concentrated in centres of plant diversity and endemism. Distribution patterns of plants mapped in the Distributiones Plantarum Africanum series and selected taxonomic monographs are analysed using the computer programme WORLDMAP. The plants are divided into four groups: herbaceous geophytes, mesophytic herbs, light-demanding shrubs and woody genera. Each group has peaks of species richness and range-size rarity at locations different to the other groups. Herbaceous geophytes and mesophytic herbs have their peaks of species richness and range-size rarity in the same location, the western Cape for geophytes and the Crystal Mountain for mesophytic herbs, whereas light-demanding shrubs and woody genera have peaks in different places. The results are discussed in relation to possible factors determining species richness and endemism and their likely conservation significance.     

Species-richness patterns of vascular plants along seven altitudinal transects in Norway

Altitudinal richness patterns were investigated along altitudinal gradients located in northern Norway (two transects) and along a west–east gradient in southern Norway (five transects). The transects were sampled for vascular plant species richness using a uniform sampling method. Each transect consisted of 38–48 5×5 m sample plots regularly spaced from sea level or valley bottom to a local mountain top. In five transects species richness peaked at mid-altitudes, whereas in the two northern transects species richness decreased with altitude. The observations were qualitatively evaluated in relation to the influence of the area of the species pool, hard boundaries, temperature and precipitation, and mass effect. The observed patterns cannot be fully accounted for by any of these factors. However, the altitude of the peak in species richness was above the forest-limit for all the humped relationships, which may suggest that species richness above the forest-limit might be enhanced by a mass effect from forest taxa. The two monotonic relationships found in the north may be caused by the relatively low number of alpine species at these sites. The monotonic pattern may result from a decrease in "forest species" towards the mountain tops.     

The influence of sampling intensity on the perception of the spatial distribution of tropical diversity and endemism: a case study of ferns from Bolivia

The distribution of tropical plant and animal diversity is still poorly documented, especially at spatial resolutions of practical use for conservation. In the present study, we evaluated the level to which geographical incomplete data availability of species occurrence affects the perception of biodiversity patterns (species richness and endemism) among pteridophytes in Bolivia. We used a data base of Bolivian pteridophytes (27,501 records), divided it into three time periods (1900–70, up to 1990 and up to 2006), and created grid-files at 15'-resolution for species richness and endemism. For each of these biodiversity properties we estimated the species richness (Chao 2) and the index of sampling completeness (C index) per grid, and then all these variables at both species richness and endemism were correlated. Patterns of richness were fairly consistent along all periods; the richest areas were placed along the humid-montane forest, even though they were strongly influenced by collecting intensity. Endemism had a lower degree of correlation with collecting intensity, but varied much more strongly through time than species richness. According to the C index, which gives the ratio between estimated (by Chao 2) and recorded values of species richness and endemism, both biodiversity properties tended to be undersampled in the richest grid cells. Inter-temporal correlations showed sharper differences of correlations for endemism than species richness. Consequently, already in 1970, botanists had a correct idea of the spatial distribution of pteridophyte richness in Bolivia (even though the magnitude was grossly underestimated). In contrast, patterns of endemism, which are of high conservation importance, may not even today be reliably known.     

Effect of sampling grain on patterns of species richness and turnover in Amazonian forests

Grain (size of sampling units) affects the spatial resolution at which ecological patterns can be observed and analysed, and potentially has an important effect on the results of broad‐scale studies on diversity gradients. Here we examine the effect of grain on patterns of species richness and turnover in lowland rainforests of western Amazonia (Peru and Colombia). We inventoried pteridophytes (ferns and lycophytes), melastomes (Melastomataceae) and palms (Arecaceae) in four line transects of 22–29 km length. Different grains were obtained by aggregating original 100‐m‐long sampling units into larger segments up to 19.2 km long. With any given grain and plant group, local species richness varied considerably both within and among transects, and a transect segment that was species‐rich with one grain could be relatively species‐poor with another. Which transect had the highest vs lowest mean species richness per sampling unit (α richness) differed among plant groups. It also varied to some degree with grain, as transects differed in how rapidly local species richness increased with increasing grain. Patterns of species turnover were more consistently correlated among plant groups than patterns of species richness were, and NMDS ordinations were rather similar with all grains and plant groups. Floristic heterogeneity within the Amazonian terra firme rainforest seems to contain a general compositional pattern that is sufficiently robust to be detectable with various sampling schemes, but patterns of species richness appear more case‐specific. Therefore, using one plant group as an indicator for patterns in other plant groups can be expected to work better for species turnover than for species richness.     

Richness and endemism of helminth parasites of freshwater fishes in Mexico

Distribution records of 152 adult helminth taxa parasites of freshwater fishes in Mexico were analysed to determine areas of high richness and endemism. Distribution maps were prepared for each taxon and overlaid onto a map of Mexico divided into 1 × 1 degree grid-cells. Richness was determined by counting recorded helminth species in each grid-cell. A corrected weighted endemism index was calculated for each grid-cell, and the relationship between richness and endemicity was analysed with an Olmstead–Tukey corner test of association. Five areas of high richness and endemism were identified: (1) Los Tuxtlas and the Papaloapan river basin, on the Gulf of Mexico; (2) the Grijalva-Usumacinta basin near the Gulf of Mexico coastal plain; (3) the Yucatan Peninsula; (4) the Sierra de Manantlán Biosphere Reserve in western Mexico; and (5) the Pátzcuaro lake, in central Mexico. The distribution of richness and endemism of helminth parasites of freshwater fishes in Mexico is congruent with distributional patterns described for other freshwater taxa in Mexico. Patterns of richness and/or endemism in the studied areas can be explained by the ichthyological composition of their bodies of water. The present study establishes an objective way of analysing the relationship between richness and endemicity, and suggests that helminths can make valuable contributions to regionalization of geographical areas and for identification of rich and biologically complex areas with potential for conservation of aquatic systems.  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 94 , 435–444.     

Diversity of Eastern North American Ant Communities along Environmental Gradients

Studies of species diversity patterns across regional environmental gradients seldom consider the impact of habitat type on within-site (alpha) and between-site (beta) diversity. This study is designed to identify the influence of habitat type across geographic and environmental space, on local patterns of species richness and regional turnover patterns of ant diversity in the northeastern United States. Specifically, I aim to 1) compare local species richness in paired open and forested transects and identify the environmental variables that best correlate with richness; and 2) document patterns of beta diversity throughout the region in both open and forested habitat. I systematically sampled ants at 67 sites from May to August 2010, spanning 10 degrees of latitude, and 1000 meters of elevation. Patterns of alpha and beta diversity across the region and along environmental gradients differed between forested and open habitats. Local species richness was higher in the low elevation and warmest sites and was always higher in open habitat than in forest habitat transects. Richness decreased as temperature decreased or elevation increased. Forested transects show strong patterns of decreasing dissimilarity in species composition between sites along the temperature gradient but open habitat transects did not. Maximum temperature of the warmest month better predicted species richness than either latitude or elevation. I find that using environmental variables as key predictors of richness yields more biologically relevant results, and produces simpler macroecological models than commonly used models which use only latitude and elevation as predictors of richness and diversity patterns. This study contributes to the understanding of mechanisms that structure the communities of important terrestrial arthropods which are likely to be influenced by climatic change.     

Centers of endemism and diversity patterns for typhlocybine leafhoppers （Hemiptera： Cicadellidae： Typhlocybinae） in China

This study identifies ＇centers of endemism＇ for typhlocybine leafhoppers in China, revealing diversity patterns and congruence of patterns between total species rich- ness and endemism. Distribution patterns of 774 Typhlocybinae （607 described and 167 undescribed species） were mapped on a 1.5° × 1.5° latitude/longitude grid. Total species richness, endemic species richness and weighted endemism richness were calculated for each grid cell. Grid cells within the top 5% highest values of weighted endemism richness were considered as ＇centers of endemism＇. Diversity patterns by latitude and altitude were obtained through calculating the gradient richness. A congruence of diversity patterns between total species richness and endemism was confirmed using correlation analysis. To investigate the bioclimatic factors （19 variables） contributing to the congruence be- tween total species richness and endemism, we compared the factor＇s difference between non-endemic and endemic species using the Kruskal-Wallis test. Eleven centers of en- demism, roughly delineated by mountain ranges, were identified in central and southern China, including the south Yunnan, Hengduan Mountains, Qinling Mountains, Hainan Is- land, Taiwan Island and six mountain areas located in western Sichuan, northwest Fujian, southeast Guizhou, southeast Hunan, central and western Guangdong, and north Zhejiang. Total species richness and endemic species richness decreased with increased latitude and had a consistent unimodal response to altitude. The proportions of endemism decreased with increased latitude and increased with rising altitude. Diversity patterns between total species richness and endemism were highly consistent, and ＇Precipitation of Coldest Pe- riod＇ and ＇Temperature of Coldest Period＇ may contribute to the congruence of pattern. Migration ability may play a role in the relationship of endemism and species richness; climate, environment factors and important geologic isolation events can also play crucial effect     

Assessing patterns of plant endemism in neotropical uplands

Conservation of biodiversity will necessitate choices among areas, taxa, and land-use patterns. Lack of data on distribution and pattern in biodiversity makes these difficult decisions even more problematic for those charged with the conservation and sustainable use of the diversity of life. Quantitative methods have promise in helping with this task in that they allow people to make their values explicit, and they also allow representation and comparison of many different types of data. In this article I examine patterns of species richness and range-size rarity, or endemism, in the Neotropics with a data set from the genusSolanum (Solanaceae). Distribution data for 180 species of forest-dwelling solanums were analyzed. Patterns of species richness, range-size rarity (endemism), and several area-selection methods were examined. Montane areas are relatively rich both in all species and in endemic species, with maximal peaks in the Andes. The peak of species richness coincides with the domain (i.e., continental) midpoint (9°30′ S latitude), suggesting that the pattern observed may be partly due to the geometry of species ranges. TheSolanum results are compared with those obtained for other taxonomic groups in the Neotropics, and problems with quantitative data sets in conservation are discussed. Collecting deficit, parochial taxonomy, and habitat destruction, both historical and current, are all factors that will affect the utility of such analyses. It is clear that if conservation is to work on the ground, we need to know more about what occurs in the montane Neotropics and that continued work at a basic taxonomic level is essential to our ultimate ability to conserve biological diversity.     

三江并流地区干旱河谷植物物种多样性海拔梯度格局比较

在滇西北三江并流地区典型干旱河谷段, 在怒江、澜沧江和金沙江的东、西坡共设置了6条海拔梯度样带, 通过标准样地的植物群落调查, 分析各条样带植物的物种丰富度、物种更替率的海拔梯度格局, 并比较了地理和植被变量对分布格局的解释。干旱河谷植被带位于海拔3,000 m以下, 以灌丛和灌草丛为主, 其在各河谷的分布上限自西向东依次升高。植物物种丰富度的分布主要与海拔、流域、经纬度和植被带有关, 沿纬度和海拔梯度升高而显著增加的格局主要表现在草本层和灌木层, 灌木物种丰富度还呈现自西向东显著增加的趋势。怒江的灌木和草本种物种丰富度显著高于金沙江和澜沧江, 三条江的乔木种丰富度差异则不显著。森林带的样方草本物种丰富度显著低于灌草丛带样方, 并且还拥有后者没有的乔木种。不同样带的植物物种更替速率呈现了不一致的海拔梯度格局, 但均在样带海拔下部的灌草丛群落与海拔上部森林群落之间的交错带出现峰值。森林-灌草丛植被交错带在怒江样带处于海拔1,900-2,100 m处, 在澜沧江河谷位于海拔2,300-2,400 m, 在金沙江河谷位于海拔2,700-2,900 m。所有海拔样带的森林段或灌草丛段相对于同一样带不同植被段之间的物种更替程度为最小, 不仅小于同一流域不同样带相同植被段之间物种更替率的均值, 更小于所有样带相同植被段之间的更替率均值。在三条河流6条海拔样带的12个植被带段之间的物种更替变化中, 空间隔离因素可以解释34.2%, 而植被类型差异仅能解释不到0.5%。本研究结果显示了环境差异对不同植被类型物种丰富度的首要影响, 和各河流之间的空间隔离对植物群落构建和物种构成的主要作用。     

Beetle species richness along the forest productivity gradient in northern Finland

The occurrence and habitat associations of the majority of invertebrate groups in boreal forests are poorly known, even though these groups represent perhaps over 99% of the animal species diversity in the forests. We studied the beetle (Coleoptera) fauna of four forest site types in northern Finland: in spruce mires, herb rich, mesic and sub-xeric forests. We sampled beetles in 32 study sites with five window and five pitfall traps in each. We describe the species abundance and diversity patterns within and among forest types and relate these patterns to structural components of the forests. The volume of decaying wood varied from 14 to 93 m³ ha⁻¹ among sampling sites. The total beetle catch consisted of 100 333 individuals and 435 species. The beetle species richness did not vary according to site fertility but the number of specimens increased with increasing fertility in heath forest sites. The richness of beetle species correlated only weakly with any of the stand structure characteristics at the stand level. Nevertheless, the detrended correspondence analysis (DCA) indicated that different beetle assemblages are characteristic of different forest types. The high level of beta-diversity in beetles among forest types indicates that focusing exclusively on, for example, key-biotopes (presumed biodiversity hotspots) when selecting areas to be set aside would result in a situation where a large proportion of species, even of the rare and threatened ones, is not included in this network of protected areas. This suggests that the complementary set of different forest types may be the best general strategy to maintain the overall beetle species diversity in boreal forests.     

Abundance, diversity and body size: patterns from a grassland arthropod community

1. The empirical relationships among body size, species richness and number of individuals may give insight into the factors controlling species diversity and the relative abundances of species. To determine these relationships, we sampled the arthropods of grasslands and savannahs at Cedar Creek, MN using sweep nets (90 525 individuals of 1225 species) and pitfall traps (12 721 individuals of 92 species). Specimens were identified, enumerated and measured to determine body size.
2. Both overall and within abundant taxonomic orders, species richness and numbers of individuals peaked at body sizes intermediate for each group. Evolution could create unimodal diversity patterns by random diversification around an ancestral body size or from size-dependent fitness differences. Local processes such as competition or predation could also create unimodal diversity distributions.
3. The average body size of a species depended significantly on its taxonomic order, but on contemporary trophic role only within the context of taxonomic order.
4. Species richness ( S _i) within size classes was related to the number of individuals ( I _i) as S _i =  I i^0·5. This relationship held across a 100 000-fold range of body sizes. Within size classes, abundance distributions of size classes were all similar power functions. A general rule of resource division, together with similar minimum population sizes, is sufficient to generate the relationship between species richness and number of individuals.
5. Smaller bodied species had slightly shallower abundance distributions and may, in general, persist at lower densities than larger species.
6. Our results suggest there may be fewer undescribed small arthropod species than previously thought and that most undescribed species will be smaller than arthropods.     

Endemism, diversity, and the threat of tropical moist forest extinctions

Extinction rates have risen to perhaps 10⁴ the background rate. Much of this increase is due to projected influences of habitat loss on regions of the world with tropical moist forest. This ecosystem, home to a disproportionate amount of global biodiversity and a major regulator of regional and global climate, also faces disproportionately severe threats. In this study, we collect diversity and endemism data for tropical forested countries of the world, along with areal and socioeconomic data. While a correlation between overall numbers of species and endemic species per country is expected, we demonstrate that endemism patterns among birds and mammals remain very strongly convergent even after statistically rendering all countries equal in size and overall species richness and after adjusting for spatial autocorrelation. On a per country basis, mammals are generally more threatened than birds in these tropical moist forested countries. Human population growth rates and rising debt among these nations should be viewed as priorities for amelioration by the developed countries. Reserve network extent is not related to numbers of endemic mammals or birds at this large spatial scale.     

Size of sampling unit strongly influences detection of seedling limitation in a wet tropical forest

Seedling limitation could structure communities, but often is evaluated with sampling units that are orders of magnitude smaller than mature plants. We censused seedlings for 5.5 years in five 1 × 200-m transects in a wet Neotropical forest. For 106 common species (≥ 10 seedlings in a transect), we calculated prevalence (occurrence of ≥ 1 newly emerged seedlings per sampling unit) at 1 m² and at 1 m × mature crown diameter units by aggregating adjacent quadrats. For most species, prevalence was 2–25% at 1 m², but 20–92% at mature crown scales. Increased prevalence arose from broadly distributed seedlings within transects, with unoccupied segments generally shorter than crown diameters. At the landscape scale, 69% of 301 species were locally rare (< 10 seedlings) and only 16% were represented in all transects (maximally separated by 2.4 km). Nonetheless, for more common species, much lower estimates of seedling limitation at mature crown scales suggest weaker influence of seedling limitation on community dynamics than previously assumed.