Differentiation diversity of Argentine cacti and its relationship to environmental factors

Abstract. We studied the differentiation diversity (β-diversity or species turnover) patterns of the three main cactus growth forms (columnar, opuntioid and globose) in 318 (1° × 1°) squares covering Argentina. We analysed the degree of association between species turnover of each growth form with the spatial variation of a set of 15 environmental variables. Species turnover was estimated in two ways: (1) by calculating species turnover along latitudinal and longitudinal gradients and (2) by evaluating the species turnover between each square and its eight surrounding neighbouring grid cells. For the three growth forms, species turnover in latitudinal transects was mostly related to the mean within-transect values of certain environmental variables, while in longitudinal transects it was related to the variation of some environmental variables within the transect rather than to their mean values. For columnar species, transect species turnover was mainly associated with variation in temperature, confirming the temperature-sensivity of this growth form. For opuntioid species, turnover along transects was mainly related to topographic variables. In the case of globose cacti, transect turnover was associated with variation in temperature and rainfall. For the three growth forms, areas of high turnover coincided with marked transitions between different biogeographic provinces, while the areas with lowest species turnover coincide with topographically and climatically uniform plains. Species turnover between individual squares was positively associated with the proportion of summer rainfall in globose cacti, the variation of mean annual temperature in columnar cacti and was negatively related to mean annual temperature in opuntioid cacti. Compared to the other growth forms, globose cacti presented a much larger proportion of squares with a high species turnover. In general, differentiation diversity was lower for the opuntioid and the columnar species, two growth forms with higher dispersal ability and was highest for the globose cacti, which have the lowest dispersal capacity. Environmentally heterogeneous areas, where large-scale transitions between biomes occur, have exceptionally high species turnover, and are important target areas for the conservation of biodiversity.     

Spatial relationships between cacti and nurse shrubs in a semi-arid environment in central Mexico

Abstract. The Zapotitlán de las Salinas valley, central Mexico, harbours a high diversity of cacti. Pattern analysis indicated that the establishment of two columnar cacti, Neobuxbaumia tetetzo and Cephalocereus hoppenstedtii, and of three small globose cacti, Coryphantapallida, Mammillaria colina andM casoi, is aggregated and associated with perennial nurse shrubs. Some nurse species, Castela tortuosa, Caesalpinia melanadenia and Eupatorium spinosarum have a higher number of cacti beneath their canopies than would be expected by chance. A replacement pattern was found between the columnar cacti and their nurses, an aspect which was not found with the globose cacti. Following the assumption that protection against excessive radiation is the main factor determining the nurse effect, the azimuth orientation of the cacti with respect to their nurses was evaluated. Only Coryphanta pallida presented a non-random distribution with a tendency towards the North and West. The difference in maximum temperature between the soil surface under the different nurse species and of open spaces, which is reached at midday, was 16 °C. No significant differences were found in beneath-canopy temperatures for the three nurse species considered. Soil nitrogen levels were significantly lower beneath the different nurse plants than in open spaces. This result suggests that soil fertility is not an important factor in the nurse-plant phenomenon in Zapotitlán.     

The importance of shrub cover for four cactus species differing in growth form in an Andean semi‐desert

Question: Factors influencing seedling establishment are known to vary between open sites and those protected by plant cover. In many desert regions, protected microhabitats below shrubs are essential for establishment of many cactus species. Very little is known about these factors for Andean cacti and how the importance of vegetation cover varies with cactus species. Are Andean cacti associated more frequently to vegetation cover than to open ground? Are they associated to certain shrub species? Is the distributional pattern in relation to cover similar for different cactus species? In what microhabitat (below or away from shrubs) are cactus seeds more abundant? These questions are addressed for the case of an Andean semi‐desert. Location: Semi‐arid tropical Andes, La Paz department, Bolivia. Methods: We examined 132 isolated shrubs = 50 cm along a line across two microhabitats: areas below and away from shrubs/trees. Shrub crown size was measured. The among‐shrub samples were taken from open spaces contiguous to each of the sampled shrubs. In both microhabitats, all cactus species were recorded. The cardinal direction of the cacti was also registered. Correlation between canopy diameter and number of beneficiaries was evaluated for Prosopis flexuosa. The cactus seed bank in each microhabitat was also studied. Results and Conclusions: The four cactus species found behaved differently in relation to shrub canopies. These distributional differences could be due to differences in growth form. Columnar cacti apparently need the shade of shrubs. Only the columnar species is able to grow near the base of the tallest nurse species. The opuntioid cacti studied seem more facultative: although apparently preferring shrub un‐der‐canopies, they are able to establish in open ground. The globose cactus is the most indifferent to the presence of plant cover. These patterns parallel others found in North America. The capacity of different cacti to appear in open spaces could be related to vegetative propagation, and not necessarily to seedling tolerance of heat.     

Climate as a determinant of dung beetle response to native forest replacement by cattle pastures in South America

Anthropogenic disturbance in natural ecosystems reduces the number of species in biological communities and homogenizes their composition across different regions. Climate is one of the main abiotic determinants of species distributions and different factors were proposed as the main climatic drivers. Here we explored the role of regional climate on the local response of dung beetle assemblages to the replacement of native forest by cattle pastures in South America by simultaneously contrasting three climatic hypotheses: energy, seasonality and heterogeneity. We compiled a database by searching published studies comparing dung beetle richness and composition between both native forests and cattle pastures. We calculated the proportional difference in species richness and composition between habitat types. As explanatory variables, we used seven abiotic variables grouped into the three climatic hypotheses. Energy/Productivity: mean annual temperature (°C/year) and total annual precipitation (mm/year). Seasonality: annual thermal amplitude (°C/year), the average coefficient of variation of monthly precipitation and the coefficient of average monthly variation in temperature. Heterogeneity: coefficient of variation of mean annual temperature, coefficient of variation of mean annual precipitation. Using regression analyses and a model selection procedure, we found differences in species richness between native forests and cattle pastures were explained by the coefficient of variation of mean annual precipitation, whereas changes in species composition were explained by total annual precipitation and the coefficient of variation of mean annual precipitation. The response of dung beetle assemblages to livestock grazing in South American forests was associated with precipitation variation. The heterogeneity hypothesis better explained changes in species richness following forest replacement by cattle pastures, while both energy/productivity and heterogeneity hypotheses explained the changes in species composition.     

Wide-band tracheids are present in almost all species of Cactaceae

Wide-band tracheids (WBTs) have been found in seedlings of most species of cacti that have fibrous wood in their adult bodies. Consequently, this cell type is now known to be present in almost all cacti. Earlier studies of adult plants revealed WBTs to be present only in cacti with globose or short, broad bodies, whereas all species with large columnar or long slender bodies had fibrous wood without WBTs. However, even these species produce WBTs during the first several months after germination. In species with fibrous wood in their adult bodies (species with large or slender bodies), seedlings undergo a phase transition in wood morphogenesis after a few months and stop producing the juvenile (WBT) wood and begin producing adult (fibrous) wood. If adult plants have an intermediate size, the phase transition is delayed and the plant produces WBT wood for several years. Species with globose bodies repress the phase transition completely and never switch to producing adult (fibrous) wood. Because WBTs are so widespread, they probably originated only once in Cactaceae, not multiple times as suggested earlier, or there may have been just a single origin in the Cactaceae/Portulacaceae clade.     

Distribution of plant life forms along an altitudinal gradient in the semi‐arid valley of Zapotitlán,Mexico

Abstract. Plant life‐form abundance along a 600 m altitudinal gradient (1600–2200 m a.s.l.) in the semi‐arid valley of Zapotitlán, México was correlated with soil characteristics and climatic variables. One mixed soil sample was taken and analysed for each of six elevations, temperature was estimated using a terrestrial thermal gradient, and precipitation using a linear regression between total annual precipitation and the elevation of the weather stations in the valley. Rosettes, microphanerophytes, therophytes and nanophanerophytes were well represented throughout the gradient. Columnar cacti were restricted to the 1600–1800 m range, and geophytes to the 1700–1800 m range. In general, abundance of life forms was inversely associated with altitude. Multiple regression analysis did not show parameters to significantly explain the abundance of rosettes, nanophanerophytes, epiphytes, geophytes and hemiparasites; altitude and nitrogen proved significant for columnar cacti, succulents and chamaephytes; altitude, pH, electrical conductivity and nitrogen were significant for globose cacti; pH was significant for therophytes; and altitude was significant for microphanerophytes.     

Identification and ecology of bacterial communities associated with necroses of three cactus species.

To compare the bacterial communities residing in necrotic tissues of columnar cacti of the Sonoran Desert, isolates from 39 organ pipe, 19 saguaro, and 16 senita cacti were obtained. The isolates were clustered into 28 conspecific groups on the basis of their fatty acid profiles. The distributions of the individual bacterial isolates varied among cactus species. Seven of the 28 species groups were unique to a particular cactus species, whereas 8 species groups were found in all three cacti. The effective number of bacterial species for each cactus species was positively correlated with both the chemical complexity and glucose concentration of the plant tissues. The effective number of bacterial species and bacterial distribution patterns were compared with those known for communities of cactophilic yeasts. The observed bacterial distribution patterns are most likely due to differences in the chemical compositions of the three cactus species.     

Time and environment explain the current richness distribution of non‐marine turtles worldwide

Ecological, historical, and evolutionary hypotheses are important to explain geographical diversity gradients in many clades, but few studies have combined them into a single analysis allowing a comparison of their relative importance. This study aimed to evaluate the relative importance of ecological, historical, and evolutionary hypotheses in explaining the current global distribution of non‐marine turtles, a group whose distribution patterns are still poorly explored. We used data from distribution range maps of 336 species of non‐marine turtles, environmental layers, and phylogeny to obtain richness estimates of these animals in 2° × 2° cells and predictors related to ecological, evolutionary and historical hypotheses driving richness patterns. Then we used a path analysis to evaluate direct and indirect effects of the predictors on turtle richness. Ancestral area reconstruction was also performed in order to evaluate the influence of time‐for‐speciation in the current diversity of the group. We found that environmental variables had the highest direct effects on non‐marine turtle richness, whereas diversification rates and area available in the last 55 million yr minimally influenced turtle distributions. We found evidence for the time‐for‐speciation effect, since regions colonized early were generally richer than recently colonized regions. In addition, regions with a high number of colonization events had a higher number of turtle species. Our results suggested that ecological processes may influence non‐marine turtle richness independent of diversification rates, but they are probably related to dispersal abilities. However, colonization time was also an important component that must be taken into account. Finally, our study provided additional support for the importance of ecological (climate and productivity) and historical (time‐for‐speciation and dispersal) processes in shaping current biodiversity patterns.     

Multiple environmental determinants of regional species richness and effects of geographic range size

Understanding patterns of species richness at broad geographic extents remains one of the most challenging yet necessary scientific goals of our time. Many hypotheses have been proposed to account for spatial variation in species richness; among them, environmental determinants have played a central role. In this study, we use data on regional bat species richness in the New World to study redundancy and complementarity of three environmental hypotheses: energy, heterogeneity and seasonality. We accomplish this by partitioning variation in species richness among components associated with unique and combined effects of variables from each hypotheses, and by partitioning the overall richness gradient into gradients of species with varying breadths of geographic distribution. These three environmental hypotheses explain most variation in the species richness gradient of all bats, but do not account for all positive spatial autocorrelation at short distances. Although environmental predictors are highly redundant, energy and seasonality explain different and complementary fractions of variation in species richness of all bats. On the other hand, heterogeneity variables contribute little to explain this gradient. However, results change dramatically when richness is estimated for groups of species with different sizes of geographic distribution. First, the amount of variation explained by environment decreases with a decrease in range size; this suggests that richness gradients of small‐ranged species can not be explained as easily as those of broadly distributed species, as has been implied by analyses that do not consider differences in range size among species. Second, the relative contribution of environmental predictors to explained variation also changes with change in range size. Seasonality and energy are good predictors of species with broad distributions, but they loose almost all explanatory power for richness of species with small ranges. In contrast, heterogeneity, which is a relatively poor predictor of richness of species with large ranges, becomes the main predictor of richness gradients of species with restricted distributions. This suggests that range size is a different dimension on which heterogeneity and other environmental characteristics are complementary to each other. Our results suggest that determinants of species richness gradients might be complex, or at least more complex than many studies have previously suggested.     

The performance of range maps and species distribution models representing the geographic variation of species richness at different resolutions

Aim The method used to generate hypotheses about species distributions, in addition to spatial scale, may affect the biodiversity patterns that are then observed. We compared the performance of range maps and MaxEnt species distribution models at different spatial resolutions by examining the degree of similarity between predicted species richness and composition against observed values from well‐surveyed cells (WSCs). Location Mexico. Methods We estimated amphibian richness distributions at five spatial resolutions (from 0.083° to 2°) by overlaying 370 individual range maps or MaxEnt predictions, comparing the similarity of the spatial patterns and correlating predicted values with the observed values for WSCs. Additionally, we looked at species composition and assessed commission and omission errors associated with each method. Results MaxEnt predictions reveal greater geographic differences in richness between species rich and species poor regions than the range maps did at the five resolutions assessed. Correlations between species richness values estimated by either of the two procedures and the observed values from the WSCs increased with decreasing resolution. The slopes of the regressions between the predicted and observed values indicate that MaxEnt overpredicts observed species richness at all of the resolutions used, while range maps underpredict them, except at the finest resolution. Prediction errors did not vary significantly between methods at any resolution and tended to decrease with decreasing resolution. The accuracy of both procedures was clearly different when commission and omission errors were examined separately. Main conclusions Despite the congruent increase in the geographic richness patterns obtained from both procedures as resolution decreases, the maps created with these methods cannot be used interchangeably because of notable differences in the species compositions they report.     

The role of nurse plants in the establishment of shrub seedlings in the semi-arid subtropical Andes

In the nurse plant syndrome, or nurse association, seedlings (beneficiaries) are associated with adult shrubs/trees (benefactors). This phenomenon has been documented in several regions of the planet. Abiotic stress amelioration (one mechanism of facilitation) is one of the causes of this association. Most of the studies addressing the nurse syndrome have been conducted on spatial scales of a few hectares and have focused on only one or a few species. Moreover, there is an almost complete lack of studies addressing the incidence and characteristics of the nurse phenomenon in the arid Andes of South America. We undertook a first approximation to the study of facilitation in these ecosystems. The study was conducted at local and regional scales and involved the assessment of the spatial distribution of juveniles (seedlings and saplings) of 51 populations of 16 shrub and 12 cactus species in relation to shrub cover at 20 localities of the Prepuna (subtropical Andes of Bolivia and Argentina, 20–26°S). In terms of spatial distribution, the juveniles of most of the populations of shrubs studied were distributed both under the shrubs and in open spaces, thereby showing an apparent indifference to microhabitat. Globose and opuntioid cacti were preferentially distributed below the canopies of shrubs and were usually more associated with the dominant shrub species, which stood out as better potential nurses. The pattern was consistent throughout the region, including the more mesic and arid localities. The fact that Prepuna woody species are capable of establishing in open spaces would confer this region a greater resilience. Our findings further suggest that community dynamics in arid and semi-arid environments are more variable than previously thought.     

Multi-extent analysis of the relationship between pteridophyte species richness and climate

Aim To determine the relationship between the distribution of climate, climatic heterogeneity and pteridophyte species richness gradients in Australia, using an approach that does not assume potential relationships are spatially invariant and allows for scale effects (extent of analysis) to be explicitly examined. Location Australia, extending from 10° S to 43° S and 112° E to 153° E. Method Species richness within 50 × 50 km grid cells was determined using point distribution data. Climatic surfaces representing the distribution and availability of water and energy at 1 km and 5 km cell resolutions were obtained. Climate at the 50 km resolution of analysis was represented by their mean and standard deviation in that area. Relationships were assessed using geographically weighted linear regression at a range of spatial bandwidths to investigate scale effects. Results The parameters and the predictive strength of all models varied across space at all extents of analysis. Overall, climatic variables representing water availability were more highly correlated to pteridophyte richness gradients in Australia than those representing energy. Their variance in cells further increased the strength of the relationships in topographically heterogeneous regions. Relationships with water were strong across all extents of analysis, particularly in the tropical and subtropical parts of the continent. Water availability explained less of the variation in richness at higher latitudes. Main conclusions This study brings into question the ability of aspatial and single‐extent models, searching for a unified explanation of macro‐scaled patterns in gradients of diversity, to adequately represent reality. It showed that, across Australia, there is a positive relationship between pteridophyte species richness and water availability but the strength and nature of the relationship varies spatially with scale in a highly complex manner. The spatial variance, or actual complexity, in these relationships could not have been demonstrated had a traditional aspatial global regression approach been used. Regional scale variation in relationships may be at least as important as more general relationships for a true understanding of the distribution of broad‐scale diversity.     

Spatial Associations, Size–Distance Relationships and Population Structure of Two Dominant Life Forms in a Semiarid Enclave of the Venezuelan Andes

The role of three thorny legume species as nurse plants and competitive relationships with columnar cacti were evaluated in a semiarid enclave of the Venezuelan Andes. Abundance and size of three columnar cacti species (Stenocereus griseus, Cereus repandus and Pilosocereus tillianus) under isolated shrubs of three thorny legumes species (Prosopis juliflora, Acacia farnesiana and A. macracantha) were recorded and compared with open areas. Using size–distance data we inferred the intensity of intra- and interspecific competition between both life forms in a “cardonal” (xeric zone) and “espinar” (mesic zone) of the enclave. Sixty-one columnar cacti were found beneath the three thorny legume species (92%), while only 5 cactus individuals were found in open areas (8%). Comparison of observed and expected number of cactus individuals shows that S. griseus and C. repandus are significantly associated with isolated shrubs of A. farnesiana and A. macracantha. Although P. juliflora contributed more than 40% of the total legume plant cover, the number of columnar cacti under its isolated shrubs was significantly lower than would be expected by chance. In all, 19 of 21 possible plant–plant combinations between and within columnar cacti and legume shrubs were recorded (espinar: 18, cardonal: 13, common combinations: 12). In both zones, intra- and interspecific combinations among columnar cacti species were relatively high (positive correlation between the sum of neighbour plant sizes and the distances separating them). Our results strongly suggest, at least for case of S. griseus and C. repandus, that these columnar cacti species require nurse plants for their establishment. The results on interference need still support from further research. We discuss the effects of plant–plant positive interactions on natural regeneration of these columnar cacti.     

Macroecological explanations for differences in species richness gradients: a canonical analysis of South American birds

Aim To evaluate how spatial variation of species richness in different bird orders responds to environmental gradients and determine which order level trait best predicts these relationships. Location South America. Methods A canonical correlation analysis was performed between the species richness in each of 17 bird orders and eight environmental variables in 374, 220 × 220 km cells. Loadings associated with the first two canonical variables were regressed against six order‐level predictors, including diversification level (number of species in each order), body size, median geographical range size and characteristics included in the model to control Type I error rates (the phylogenetic relationship among orders and levels of local‐scale spatial autocorrelation). Results Richness patterns of 14 bird orders were highly correlated with the first canonical axis, indicating that most orders respond similarly to energy‐water gradients (primarily actual evapotranspiration, minimum temperature and potential evapotranspiration). In contrast, species richness within Trochiliformes, Apodiformes and Galliformes were also correlated with the second canonical variable, representing measures of mesoscale climatic variation (range in elevation within cells, minimum temperature, and the interaction term between them) and landcover (habitat diversity). We also found that total diversification within orders was the best predictor of the loadings associated with the first canonical axis, whereas body size of each order best predicted loadings on the second axis. Conclusion Our results broadly support climatic‐related hypotheses as explanations for spatial variation in species richness of different orders. However, both historical (order‐specific variation in speciation rates) and ecological (dispersal of species that evolved by independent processes into areas amenable to birds) processes can explain the relationship between order level traits, such as body size and diversification level, and magnitude of response to current environment, furnishing then guidelines for a further and deeper understanding of broad‐scale diversity gradients.     

Analysis of the community structure of yeasts associated with the decaying stems of cactus. II.Opuntia species

A survey was made of yeast species associated with the decaying pads of 3 prickly pear cacti (Opuntia phaeacantha, O. ficus-indica, andO. lindheimeri) in Arizona and Texas. Yeast communities from 12 localities were compared among localities, amongOpuntia species, and with previous data on yeast communities associated with columnar cacti. The results indicate thatOpuntia necroses contain relatively more yeast species with broader physiological abilities in their communities than columnar necroses. It is argued that differences in chemistry of the opuntias and columnar forms in concert with the insect vectors specific for these cacti account for the differences in yeast community structure. It is further hypothesized that the differences in yeast community structure have been important in the evolution and maintenance of species diversity forDrosophila species which live in the decaying stems or cladodes of various cacti. Most of the yeast community evolution in the cacti is postulated to have proceeded by evolution in situ and not by additions and replacements from outside of the system.     

Effect of light on seed germination and seedling shape of succulent species from Mexico

Aims Light requirements for cactus seed germination have been considered to be associated with their adult plant height and seed mass, but this has not been thoroughly studied for other succulent species. In order to understand seed photosensitivity from desert species belonging to Asparagaceae (subfamily Agavoideae) and Cactaceae, we performed a germination experiment with and without light for 12 species and 2 varieties from 1 species from the Southern Chihuahuan Desert. We also determined if adult growth is totally determined by seedling 'growth form' in cacti.Methods We performed a germination experiment using light and darkness for 13 species from Southern Chihuahuan Desert: 10 rosette species (Asparagaceae), as well as 1 globose, 1 columnar and 2 varieties from 1 depressed-globose species (Cactaceae). The response variables were seed germination percentage and relative light germination (RLG). In addition, in order to determine if adult-globose cacti could have cylindrical seedlings, we calculated the shape index (height/width ratio) for Coryphanta clavata and Mammillaria compressa .Important findings All species were considered neutral photoblastic. Eleven species had similar seed germination in both light and dark conditions, and three taxa (M. compressa and the two varieties of Ferocactus latispinus) showed higher germination with light than without it. Agave salmiana, M. compressa and the two varieties of F. latispinus had higher RLG than the other species. Seed mass was an important factor because with higher seed mass there was lower dependence to light. These findings support the hypothesis that small seed mass and light requirements have coevolved as an adaptation to ensure germination. One adult-globose cactus species, M. compressa, and one adult-columnar species, C. clavata, had small seeds and neutral fotoblasticism. Seedlings from these two species exposed to light were cylindrical and those under darkness conditions were columnar. Perhaps seeds from this species are able to germinate in the dark because they produce columnar seedlings with the ability to emerge from greater soil depths where sunlight cannot penetrate.     

Latitudinal gradient in species richness of the New World Triatominae (Reduviidae)

Aim To quantify the latitudinal gradient in species richness in the New World Triatominae and to explore the species‐energy and area hypotheses as possible causes. Location The gradient was studied for North and South America, between 43° N and 32° S. Methods A database was constructed containing the geographical distribution of the 118 New World Triatominae species based on data extracted from several published sources. Species richness was recorded as the number of species present within 5° latitudinal bands. We used univariate and multivariate models to analyse the relationship between area within each latitudinal belt, land surface temperature, and potential evapotranspiration as explanatory variables, and species richness. All variables were georeferenced and data were extracted using a GIS. Results Species richness of Triatominae increases significantly from the poles towards the Equator, peaking over the 5°?10 ° S latitudinal band. It increases according to a linear model, both north and south of the Equator, although a quadratic model fits better to southern hemisphere data. Richness correlates with habitable geographical area, when it is analysed through a nonlinear multiple regression factoring out latitude, only in the southern hemisphere. Regarding the species‐energy hypothesis, a multiple regression analysis controlling the effect of latitude shows a significant relationship between temperature and species richness. This effect is more pronounced in the southern hemisphere. Species richness shows a strong longitudinal trend south of the Equator (increasing to the east), but not north of the Equator. This differential pattern is reflected in significant interactions between longitude and both latitude and temperature in models of the species richness of the New World Triatominae. Main conclusions To our knowledge, this is the first time that a latitudinal gradient in species richness has been shown and analysed for obligate haematophagous organisms, and it shows that the species–energy hypothesis can account for this phenomenon. This relationship is stronger in the southern hemisphere.     

Seedling survival of three endemic and threatened Mexican cacti under induced climate change

Human‐induced warming may increase the risk of local extinction for plant species with low tolerance of elevated temperatures. The Chihuahuan desert harbors the highest diversity of globose cacti in the world and most of them are at risk of extinction. Predictive models of climate change indicate an increase in summer temperature of 1–2°C by 2030 for this desert. Nevertheless, studies on the vulnerability of cacti species in early development phases to future climate change are scarce. We assessed the survival of three threatened cacti species from the Chihuahuan desert under induced warming. Open‐top chambers (OTCs) were used to simulate the effect of global warming on 2‐year seedlings of Echinocactus platyacanthus f. visnaga, Ferocactus histrix and Stenocactus coptonogonus. OTCs had higher temperature and lower humidity than control plots, and these elevated temperatures reduced seedling survival. Within the OTCs, no living individuals of any species were found after 105 days. Conversely, in the control plots, the three cacti species showed variable numbers of survivors after this period. Therefore the predicted global warming scenarios will greatly limit plant recruitment and the long‐term persistence of natural populations of Mexican endemic cacti species.     

High tropical net diversification drives the New World latitudinal gradient in palm (Arecaceae) species richness

Aim Species richness exhibits striking geographical variation, but the processes that drive this variation are unresolved. We investigated the relative importance of two hypothesized evolutionary causes for the variation in palm species richness across the New World: time for diversification and evolutionary (net diversification) rate. Palms have a long history in the region, with the major clades diversifying during the Tertiary (65–2 Ma). Location Tropical and subtropical America (34° N–34° S; 33–120° W). Methods Using range maps, palm species richness was estimated in a 1° × 1° grid. Mean lineage net diversification was estimated by the mean phylogenetic root distance (MRD), the average number of nodes separating a species from the base of the palm phylogeny for the species in each grid cell. If evolutionary rate limits richness, then richness should increase with MRD. If time limits richness, then old, relict species (with low root distance) should predominantly occur in long‐inhabited and therefore species‐rich areas. Hence, richness should decrease with MRD. To determine the influence of net diversification across different time frames, MRD was computed for subtribe, genus and species levels within the phylogeny, and supplemented with the purely tip‐level measure, mean number of species per genus (MS/G). Correlations and regressions, in combination with eigenvector‐based spatial filtering, were used to assess the relationship between species richness, the net diversification measures, and potential environmental and geographical drivers. Results Species richness increased with all net diversification measures. The regression models showed that richness and the net diversification measures increased with decreasing (absolute) latitude and, less strongly, with increasing energy/temperature and water availability. These patterns therefore reflect net diversification at both deep and shallow levels in the phylogeny. Richness also increased with range in elevation, but this was only reflected in the MS/G pattern and therefore reflects recent diversification. Main conclusions The geographical patterns in palm species richness appear to be predominantly the result of elevated net diversification rates towards the equator and in warm, wet climates, sustained throughout most of the Tertiary. Late‐Tertiary orogeny has caused localized increases in net diversification rates that have also made a mark on the richness pattern.