scholarly journals Can net diversification rates account for spatial patterns of species richness?

2017 ◽  
Author(s):  
Camilo Sanín ◽  
Iván Jiménez ◽  
Jon Fjeldså ◽  
Carsten Rahbek ◽  
Carlos Daniel Cadena

ABSTRACTThe diversification rate hypothesis (DRH) proposes that spatial patterns of species richness result from spatial variation in net diversification rates. We developed an approach using a time-calibrated phylogeny and distributional data to estimate the maximum explanatory power of the DRH, over a given time period, to current species richness in an area. We used this approach to study species richness patterns of a large family of suboscine birds across South America. The maximum explanatory power of the DRH increased with the duration of the time period considered and grain size; it ranged from 13 – 37 fold local increases in species richness for T = 33 Ma to less than 2-fold increases for T ≤ 10 Ma. For large grain sizes (≤ 8° × 8°) diversification rate over the last 10 Ma could account for all the spatial variance in species richness, but for smaller grain sizes commonly used in biogeographical studies (1° × 1°), it could only explain < 16% of this variance. Thus, diversification since the Late Miocene, often thought to be a major determinant of Neotropical diversity, had a limited imprint on spatial richness patterns at small grain sizes. Further application of our approach will help determine the role of the DRH in explaining current spatial patterns of species richness.Note to readersThis manuscript has been seen by a few researchers, some of whom suggested that before publishing our work in a peer-reviewed journal we should conduct simulations to demonstrate that our methods properly estimate the contribution of variance in diversification rates to spatial variation in species richness. Although we believe that our approach derives logically from theory and statistics and is therefore valid, we understand that it is rather unique and see why some readers would think that an independent validation is necessary. Unable to complete such validation in the near future, however, we decided to make this manuscript available as a preprint to share our ideas and hopefully stimulate discussion on what we believe is a most interesting topic. We also hope to receive feedback that may enable us to improve our work for publication in a journal at a later date.

2015 ◽  
Vol 11 (7) ◽  
pp. 20150506 ◽  
Author(s):  
John J. Wiens

The major clades of vertebrates differ dramatically in their current species richness, from 2 to more than 32 000 species each, but the causes of this variation remain poorly understood. For example, a previous study noted that vertebrate clades differ in their diversification rates, but did not explain why they differ. Using a time-calibrated phylogeny and phylogenetic comparative methods, I show that most variation in diversification rates among 12 major vertebrate clades has a simple ecological explanation: predominantly terrestrial clades (i.e. birds, mammals, and lizards and snakes) have higher net diversification rates than predominantly aquatic clades (i.e. amphibians, crocodilians, turtles and all fish clades). These differences in diversification rates are then strongly related to patterns of species richness. Habitat may be more important than other potential explanations for richness patterns in vertebrates (such as climate and metabolic rates) and may also help explain patterns of species richness in many other groups of organisms.


2007 ◽  
Vol 76 (3) ◽  
pp. 197-204 ◽  
Author(s):  
M. Aliabadian ◽  
C. S. Roselaar ◽  
R. Sluys ◽  
V. Nijman

In the study of diversity patterns, the Mid-domain effect (MDE), which explains gradients in diversity solely on the basis of geometric constraints, has emerged as a null-model against which other hypotheses can be tested. The effectiveness, measured by its predictive power, of these MDE models appears to depend on the size of the study area and the range-sizes of the taxa considered. Here we test the predictive power of MDE on the species richness patterns of birds and assess its effectiveness for a variety of species range sizes. We digitised distribution maps of 889 species of songbird endemic to the Palearctic, and analysed the emergent biogeographic patterns with WORLDMAP software. MDE had a predictive power of 20% when all songbirds were included. Major hotspots were located south of the area where MDE predicted the highest species-richness, and some of the observed coldspots were in the centre of the Palearctic, contradicting the predictions of the MDE. MDE had little explanatory power (3-19%) for all but the largest range sizes, whereas MDE performed equal or better for the large-ranged species (20-34%) compared to the overall model. Overall MDE did not accurate explain species-richness patterns in Palearctic songbirds. Subsets of larger-range species did not always have a larger predictive power than smaller-range species or the overall model. Despite their low predictive power, MDE models can have a role to play in explaining biogeographic patterns but other variables need to be included in the model as well.


2016 ◽  
Vol 283 (1838) ◽  
pp. 20161334 ◽  
Author(s):  
Joshua P. Scholl ◽  
John J. Wiens

Species richness varies dramatically among clades across the Tree of Life, by over a million-fold in some cases (e.g. placozoans versus arthropods). Two major explanations for differences in richness among clades are the clade-age hypothesis (i.e. species-rich clades are older) and the diversification-rate hypothesis (i.e. species-rich clades diversify more rapidly, where diversification rate is the net balance of speciation and extinction over time). Here, we examine patterns of variation in diversification rates across the Tree of Life. We address how rates vary across higher taxa, whether rates within higher taxa are related to the subclades within them, and how diversification rates of clades are related to their species richness. We find substantial variation in diversification rates, with rates in plants nearly twice as high as in animals, and rates in some eukaryotes approximately 10-fold faster than prokaryotes. Rates for each kingdom-level clade are then significantly related to the subclades within them. Although caution is needed when interpreting relationships between diversification rates and richness, a positive relationship between the two is not inevitable. We find that variation in diversification rates seems to explain most variation in richness among clades across the Tree of Life, in contrast to the conclusions of previous studies.


2012 ◽  
Vol 2012 ◽  
pp. 1-12 ◽  
Author(s):  
Jörn Buse ◽  
Eva Maria Griebeler

Applying multiple generalized regression models, we studied spatial patterns in species richness for different taxonomic groups (amphibians, reptiles, grasshoppers, plants, mosses) within the German federal state Rhineland-Palatinate (RP). We aimed (1) to detect their centres of richness, (2) to rate the influence of climatic and land-use parameters on spatial patterns, and (3) to test whether patterns are congruent between taxonomic groups in RP. Centres of species richness differed between taxonomic groups and overall richness was the highest in the valleys of large rivers and in different areas of southern RP. Climatic parameters strongly correlated with richness in all taxa whereas land use was less significant. Spatial richness patterns of all groups were to a certain extent congruent but differed between group pairs. The number of grasshoppers strongly correlated with the number of plants and with overall species richness. An external validation corroborated the generality of our species richness models.


2019 ◽  
Author(s):  
Elizabeth Christina Miller ◽  
Cristian Román-Palacios

AbstractAimThe evolutionary causes of the latitudinal diversity gradient are debated. Hypotheses have ultimately invoked either faster rates of diversification in the tropics, or more time for diversification due to the tropical origins of higher taxa. Here we perform the first test of the diversification rate and time hypotheses in freshwater ray-finned fishes, a group comprising nearly a quarter of all living vertebrates.LocationGlobal.Time period368–0 mya.Major taxa studiedExtant freshwater ray-finned fishes.MethodsUsing a mega-phylogeny of actinopterygian fishes and a global database of occurrence records, we estimated net diversification rates, the number of colonizations and regional colonization times of co-occurring species in freshwater drainage basins. We used Generalized Additive Models to test whether these factors were related to latitude. We then compared the influence of diversification rates, colonization numbers, colonization times and surface area on species richness, and how these factors are related to each other.ResultsWhile both diversification rates and time were related to richness, time had greater explanatory power and was more strongly related to latitude than diversification rates. Other factors (basin surface area, number of colonizations) also helped explain richness but were unrelated to latitude. The world’s most diverse freshwater basins (Amazon, Congo rivers) were dominated by lineages with Mesozoic origins. The temperate groups dominant today arrived near the K-Pg boundary, leaving comparatively less time to build richness. Diversification rates and colonization times were inversely related: recently colonized basins had the fastest rates, while ancient species-rich faunas had slower rates.Main conclusionsWe concluded that time is the lead driver of latitudinal richness disparities in freshwater fish faunas. We suggest that the most likely path to building very high species richness is through diversification over long periods of time, rather than diversifying quickly.


2012 ◽  
Vol 279 (1745) ◽  
pp. 4148-4155 ◽  
Author(s):  
Víctor Soria-Carrasco ◽  
Jose Castresana

The latitudinal gradient of species richness has frequently been attributed to higher diversification rates of tropical groups. In order to test this hypothesis for mammals, we used a set of 232 genera taken from a mammalian supertree and, additionally, we reconstructed dated Bayesian phylogenetic trees of 100 genera. For each genus, diversification rate was estimated taking incomplete species sampling into account and latitude was assigned considering the heterogeneity in species distribution ranges. For both datasets, we found that the average diversification rate was similar among all latitudinal bands. Furthermore, when we used phylogenetically independent contrasts, we did not find any significant correlation between latitude and diversification parameters, including different estimates of speciation and extinction rates. Thus, other factors, such as the dynamics of dispersal through time, may be required to explain the latitudinal gradient of diversity in mammals.


Diversity ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 275
Author(s):  
Mariana A. Tsianou ◽  
Maria Lazarina ◽  
Danai-Eleni Michailidou ◽  
Aristi Andrikou-Charitidou ◽  
Stefanos P. Sgardelis ◽  
...  

The ongoing biodiversity crisis reinforces the urgent need to unravel diversity patterns and the underlying processes shaping them. Although taxonomic diversity has been extensively studied and is considered the common currency, simultaneously conserving other facets of diversity (e.g., functional diversity) is critical to ensure ecosystem functioning and the provision of ecosystem services. Here, we explored the effect of key climatic factors (temperature, precipitation, temperature seasonality, and precipitation seasonality) and factors reflecting human pressures (agricultural land, urban land, land-cover diversity, and human population density) on the functional diversity (functional richness and Rao’s quadratic entropy) and species richness of amphibians (68 species), reptiles (107 species), and mammals (176 species) in Europe. We explored the relationship between different predictors and diversity metrics using generalized additive mixed model analysis, to capture non-linear relationships and to account for spatial autocorrelation. We found that at this broad continental spatial scale, climatic variables exerted a significant effect on the functional diversity and species richness of all taxa. On the other hand, variables reflecting human pressures contributed significantly in the models even though their explanatory power was lower compared to climatic variables. In most cases, functional richness and Rao’s quadratic entropy responded similarly to climate and human pressures. In conclusion, climate is the most influential factor in shaping both the functional diversity and species richness patterns of amphibians, reptiles, and mammals in Europe. However, incorporating factors reflecting human pressures complementary to climate could be conducive to us understanding the drivers of functional diversity and richness patterns.


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