The positive relationship between relief and species richness in mesophotic communities on offshore banks, including geographic patterns

2016 ◽  
Vol 23 (4) ◽  
pp. 195-207 ◽  
Author(s):  
Paul W. Sammarco ◽  
Marissa F. Nuttall ◽  
Daniel Beltz ◽  
L. Horn ◽  
G. Taylor ◽  
...  
2020 ◽  
Vol 7 (7) ◽  
pp. 192045
Author(s):  
Faith A. M. Jones ◽  
Maria Dornelas ◽  
Anne E. Magurran

As pressures on biodiversity increase, a better understanding of how assemblages are responding is needed. Because rare species, defined here as those that have locally low abundances, make up a high proportion of assemblage species lists, understanding how the number of rare species within assemblages is changing will help elucidate patterns of recent biodiversity change. Here, we show that the number of rare species within assemblages is increasing, on average, across systems. This increase could arise in two ways: species already present in the assemblage decreasing in abundance but with no increase in extinctions, or additional species entering the assemblage in low numbers associated with an increase in immigration. The positive relationship between change in rarity and change in species richness provides evidence for the second explanation, i.e. higher net immigration than extinction among the rare species. These measurable changes in the structure of assemblages in the recent past underline the need to use multiple biodiversity metrics to understand biodiversity change.


Water ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 2170
Author(s):  
Elzbieta Dumnicka ◽  
Tanja Pipan ◽  
David Culver

Caves are the best studied aquatic subterranean habitat, but there is a wide variety of these habitats, ranging in depth below the surface and size of the spaces (pore or habitat size). Both factors are important in setting limits to species composition and richness. In addition to caves, among the most important shallow aquatic subterranean habitats are the hyporheal (underflow of rivers and streams), the hypotelminorheal (very superficial drainages with water exiting in seeps), epikarst, and calcrete aquifers. Although it is little studied, both body size and species composition in the different habitats is different. Because of high levels of endemism and difficulty in access, no subterranean habitats are well sampled, even caves. However, there are enough data for robust generalizations about some geographic patterns. Individual hotspot caves are concentrated in the Dinaric region of southern Europe, and overall, tropical regions have fewer obligate aquatic cave dwellers (stygobionts). In all subterranean aquatic habitats, regional diversity is much higher than local diversity, but local diversity (especially single cave diversity) may be a useful predictor of regional species richness. In Europe there is a ridge of high aquatic subterranean species richness basically extending east from the French–Spanish border. Its cause may be either high productivity or that long-term temperature oscillations are at a minimum. With increased collecting and analysis, global and continental trends should become clearer.


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.


Oryx ◽  
2019 ◽  
pp. 1-10 ◽  
Author(s):  
Maria Therese Bager Olsen ◽  
Jonas Geldmann ◽  
Mike Harfoot ◽  
Derek P. Tittensor ◽  
Becky Price ◽  
...  

AbstractThe USA is the largest consumer of legally, internationally-traded wildlife. A proportion of this trade consists of species listed in the Appendices of CITES, and recorded in the CITES Trade Database. Using this resource, we quantified wildlife entering the USA for 82 of the most frequently recorded wildlife products and a range of taxonomic groups during 1979–2014. We examined trends in legal trade and seizures of illegally traded items over time, and relationships between trade and four national measures of biodiversity. We found that: (1) there is an overall positive relationship between legal imports and seizures; (2) Asia was the main region exporting CITES-listed wildlife products to the USA; (3) bears, crocodilians and other mammals (i.e. other than Ursidae, Felidae, Cetacea, Proboscidea, Primates or Rhinocerotidae) increased in both reported legal trade and seizures over time; (4) legal trade in live specimens was reported to be primarily from captive-produced, artificially-propagated or ranched sources, whereas traded meat was primarily wild sourced; (5) both seizures and legally traded items of felids and elephants decreased over time; and (6) volumes of both legally traded and seized species were correlated with four attributes of exporting countries: species endemism, species richness, number of IUCN threatened species, and country size. The goal of our analysis was to inform CITES decision-making and species conservation efforts.


2020 ◽  
Vol 117 (27) ◽  
pp. 15450-15459 ◽  
Author(s):  
Torben Riehl ◽  
Anne-Cathrin Wölfl ◽  
Nico Augustin ◽  
Colin W. Devey ◽  
Angelika Brandt

Habitat heterogeneity and species diversity are often linked. On the deep seafloor, sediment variability and hard-substrate availability influence geographic patterns of species richness and turnover. The assumption of a generally homogeneous, sedimented abyssal seafloor is at odds with the fact that the faunal diversity in some abyssal regions exceeds that of shallow-water environments. Here we show, using a ground-truthed analysis of multibeam sonar data, that the deep seafloor may be much rockier than previously assumed. A combination of bathymetry data, ruggedness, and backscatter from a trans-Atlantic corridor along the Vema Fracture Zone, covering crustal ages from 0 to 100 Ma, show rock exposures occurring at all crustal ages. Extrapolating to the whole Atlantic, over 260,000 km2of rock habitats potentially occur along Atlantic fracture zones alone, significantly increasing our knowledge about abyssal habitat heterogeneity. This implies that sampling campaigns need to be considerably more sophisticated than at present to capture the full deep-sea habitat heterogeneity and biodiversity.


1988 ◽  
Vol 36 (4) ◽  
pp. 385 ◽  
Author(s):  
BR Maslin ◽  
L Pedley

Patterns of distribution are described for the three subgenera and nine sections that make up the Australian Acacia flora. Subgenus Phyllodineae (833 species) is widespread and contains 99% of the species; subgenus Acacia (six species) and subgenus Aculeiferum (one species) are poorly represented and virtually confined to the north of the continent. The geographic patterns of species-richness are strongly influenced by sections Phyllodineae (352 species), Juliflorae (219 species) and Plurinerves (178 species). Section Phyllodineae has centres of richness south of the Tropic of Capricorn in temperate and adjacent semiarid areas of eastern, south-eastern and south-western Australia. The section is poorly represented in the tropics. The closely related sections Juliflorae and Plurinerves predominate in the north of the continent, semiarid areas of the south-west, many rocky tablelands of the Arid Zone and along the Great Dividing Range and adjacent inland riverine lowland areas in eastern Australia. The remaining four sections contribute little to the overall patterns of species-richness. The principal speciespoor areas are sandy and fluvial lowland regions of the Arid Zone. In eastern Australia, sections Botrycephalae, Juliflorae, Phyllodineae and Plurinerves show discontinuous patterns of species-richness along the Great Dividing Range. All sections have species whose ranges terminate in the area of the McPherson-Macleay Overlap region.


2016 ◽  
Vol 36 (23) ◽  
Author(s):  
沈梦伟 SHEN Mengwei ◽  
陈圣宾 CHEN Shengbin ◽  
毕孟杰 BI Mengjie ◽  
陈文德 CHEN Wende ◽  
周可新 ZHOU Kexin

2010 ◽  
Vol 6 (4) ◽  
pp. 490-493 ◽  
Author(s):  
Terrence P. McGlynn ◽  
Michael D. Weiser ◽  
Robert R. Dunn

A positive relationship between species richness and productivity is often observed in nature, but the causes remain contentious. One mechanism, the ‘more individuals hypothesis’ (MIH), predicts richness increases monotonically with density, as a function of resource flux. To test the MIH, we manipulated resource abundance in a community of tropical rainforest litter ants and measured richness and density responses. A unimodal relationship between richness and density most closely fitted the control and disturbance (resource removal) treatments in contrast to expectations of the MIH. Resource addition resulted in a monotonic increase in richness relative to density, a shift from the pattern in the control. In the disturbance treatment, richness was greater than in the control, opposite to expectations of the MIH. While large-scale correlations between ant diversity and net primary productivity or temperature are reconcilable with the MIH, key elements of the hypothesis are not supported.


2015 ◽  
Vol 31 (1) ◽  
pp. 111-115 ◽  
Author(s):  
Giuliano Milana ◽  
Manuela Lai ◽  
Luigi Maiorano ◽  
Luca Luiselli ◽  
Giovanni Amori

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