scholarly journals Reconciliation ecology and the future of species diversity

Oryx ◽  
2003 ◽  
Vol 37 (2) ◽  
pp. 194-205 ◽  
Author(s):  
Michael L. Rosenzweig
Keyword(s):  
Steady State ◽  
Species Diversity ◽  
Natural Area ◽  
Reconciliation Ecology ◽  
Anthropogenic Habitats ◽  
Extinction Rates ◽  
Broad Array ◽  
Speciation Rates ◽  
Species Area ◽  
Biogeographical Province

Species-area relationships (SPARs) dictate a sea change in the strategies of biodiversity conservation. SPARs exist at three ecological scales: Sample-area SPARs (a larger area within a biogeographical province will tend to include more habitat types, and thus more species, than a smaller one), Archipelagic SPARs (the islands of an archipelago show SPARs that combine the habitat-sampling process with the problem of dispersal to an island), and Interprovincial SPARs (other things being equal, the speciation rates of larger biogeographical provinces are higher and their extinction rates are lower, leading to diversities in proportion to provincial area). SPARs are the products of steady-state dynamics in diversity, and such dynamics appears to have characterized the earth for most of the last 500 million years. As people reduce the area available to wild species, they impose a linear reduction of the earth's species diversity that will follow the largest of these scales, i.e. each 1% reduction of natural area will cost about 1% of steady-state diversity. Reserving small tracts of wild habitat can only delay these reductions. But we can stop most of them by redesigning anthropogenic habitats so that their use is compatible with use by a broad array of other species. That is reconciliation ecology. Many pilot projects, whether intentionally or inadvertently espousing reconciliation ecology, are demonstrating that it can be done.

scholarly journals How humans drive speciation as well as extinction

2016 ◽  
Vol 283 (1833) ◽  
pp. 20160600 ◽  
Author(s):  
J. W. Bull ◽  
M. Maron
Keyword(s):  
Species Diversity ◽  
Human Activities ◽  
Rapid Evolution ◽  
Novel Ecosystem ◽  
No Net Loss ◽  
Extinction Rates ◽  
Trade Offs ◽  
Speciation Rates ◽  
Nuanced Understanding ◽  
Comparable Magnitude

A central topic for conservation science is evaluating how human activities influence global species diversity. Humanity exacerbates extinction rates. But by what mechanisms does humanity drive the emergence of new species? We review human-mediated speciation, compare speciation and known extinctions, and discuss the challenges of using net species diversity as a conservation objective. Humans drive rapid evolution through relocation, domestication, hunting and novel ecosystem creation—and emerging technologies could eventually provide additional mechanisms. The number of species relocated, domesticated and hunted during the Holocene is of comparable magnitude to the number of observed extinctions. While instances of human-mediated speciation are known, the overall effect these mechanisms have upon speciation rates has not yet been quantified. We also explore the importance of anthropogenic influence upon divergence in microorganisms. Even if human activities resulted in no net loss of species diversity by balancing speciation and extinction rates, this would probably be deemed unacceptable. We discuss why, based upon ‘no net loss’ conservation literature—considering phylogenetic diversity and other metrics, risk aversion, taboo trade-offs and spatial heterogeneity. We conclude that evaluating speciation alongside extinction could result in more nuanced understanding of biosphere trends, clarifying what it is we actually value about biodiversity.

Taxonomic evolution in North American Neogene horses (subfamily Equinae): the rise and fall of an adaptive radiation

Paleobiology ◽  
1993 ◽  
Vol 19 (2) ◽  
pp. 216-234 ◽  
Author(s):  
Richard C. Hulbert
Keyword(s):  
Species Richness ◽  
Steady State ◽  
Adaptive Radiation ◽  
Middle Miocene ◽  
Extinction Rate ◽  
Extinction Rates ◽  
Speciation Rates ◽  
History Of ◽  
Very High ◽  
Radiation Phase

The 18 m.y. history of the subfamily Equinae (exclusive of Archaeohippus and “Parahippus”) in North America consisted of a 3-m.y. radiation phase, a 9-m.y. steady-state diversity phase, and a 6-m.y. reduction phase. During the steady-state phase, species richness varied between 14 and 20, with two maxima at about 13.5 and 6.5 Ma. Species richness of the tribes Hipparionini and Equini was about equal through the middle Miocene, but hipparionines consistently had more species in the late Miocene and early Pliocene. Overall mean species duration was 3.2 m.y. (n = 50), or an average extinction rate of 0.31 m.y.-1 During the radiation phase, speciation rates were very high (0.5 to 1.4 m.y.-1), while extinction rates were low (<0.10 m.y.-1). Speciation and extinction rates both averaged about 0.15 m.y.-1 during the steady-state phase, with extinction rates having more variation. Extinction rates increased fourfold during the reduction phase, while speciation rates declined slightly. Late Hemphillian extinctions affected both tribes severely, not just the three-toed hipparionines, and were correlated with global climatic change.

scholarly journals Hybridizing salamanders experience accelerated diversification

2019 ◽  
Author(s):  
Austin H. Patton ◽  
Mark J. Margres ◽  
Brendan Epstein ◽  
Jon Eastman ◽  
Luke J. Harmon ◽  
...  
Keyword(s):  
Species Diversity ◽  
Strong Evidence ◽  
Diversification Rates ◽  
Extinction Rates ◽  
Speciation Rates ◽  
Evolutionary Role ◽  
Taxonomic Order

ABSTRACTWhether hybridization generates or erodes species diversity has long been debated, but to date most studies have been conducted at small taxonomic scales. Salamanders (order Caudata) represent a taxonomic order in which hybridization plays a prevalent ecological and evolutionary role. We employed a recently developed model of trait-dependent diversification to test the hypothesis that hybridization impacts the diversification dynamics of species that are currently hybridizing. We find strong evidence supporting this hypothesis, showing that hybridizing salamander lineages have significantly greater net-diversification rates than non-hybridizing lineages. This pattern is driven by concurrently increased speciation rates and decreased extinction rates in hybridizing lineages. Our results support the hypothesis that hybridization can act as a generative force in macroevolutionary diversification.

scholarly journals Geographic contingency, not species sorting, dominates macroevolutionary dynamics in an extinct clade of neogastropods (Volutospina; Volutidae)

Paleobiology ◽  
2021 ◽  
pp. 1-15
Author(s):  
Dana S. Friend ◽  
Brendan M. Anderson ◽  
Warren D. Allmon
Keyword(s):  
Middle Eocene ◽  
Ecological Factors ◽  
Geographic Range ◽  
Late Eocene ◽  
Range Size ◽  
Species Sorting ◽  
Extinction Rates ◽  
Geographic Range Size ◽  
Speciation Rates ◽  
Planktotrophic Larvae

Abstract Rates of speciation and extinction are often linked to many ecological factors, traits (emergent and nonemergent) such as environmental tolerance, body size, feeding type, and geographic range. Marine gastropods in particular have been used to examine the role of larval dispersal in speciation. However, relatively few studies have been conducted placing larval modes in species-level phylogenetic context. Those that have, have not incorporated fossil data, while landmark macroevolutionary studies on fossil clades have not considered both phylogenetic context and net speciation (speciation–extinction) rates. This study utilizes Eocene volutid Volutospina species from the U.S. Gulf Coastal Plain and the Hampshire Basin, U.K., to explore the relationships among larval mode, geographic range, and duration. Based on the phylogeny of these Volutospina, we calculated speciation and extinction rates in order to compare the macroevolutionary effects of larval mode. Species with planktotrophic larvae had a median duration of 9.7 Myr, which compared significantly to 4.7 Myr for those with non-planktotrophic larvae. Larval mode did not significantly factor into geographic-range size, but U.S. and U.K. species do differ, indicating a locality-specific component to maximum geographic-range size. Non-planktotrophs (NPTs)were absent among the Volutospina species during the Paleocene–early Eocene. The relative proportions of NPTs increased in the early middle Eocene, and the late Eocene was characterized by disappearance of planktotrophs (PTs). The pattern of observed lineage diversity shows an increasing preponderance of NPTs; however, this is clearly driven by a dramatic extinction of PTs, rather than higher NPT speciation rates during the late Eocene. This study adds nuance to paleontology's understanding of the macroevolutionary consequences of larval mode.

SPECIES DIVERSITY PATTERNS DERIVED FROM SPECIES–AREA MODELS

Ecology ◽  
2002 ◽  
Vol 83 (5) ◽  
pp. 1185-1198 ◽  
Author(s):  
Fangliang He ◽  
Pierre Legendre
Keyword(s):  
Species Diversity ◽  
Diversity Patterns ◽  
Species Area

scholarly journals TREE SPECIES DIVERSITY IN A PRISTINE MONTANE FOREST PREVIOUSLY UNTOUCHED BY HUMAN ACTIVITIES IN FOJA MOUNTAINS, PAPUA, INDONESIA

REINWARDTIA ◽  
2018 ◽  
Vol 17 (2) ◽  
Author(s):  
Asep Sadili ◽  
Kuswata Kartawinata ◽  
Herwasono Soedjito ◽  
Edy Nasriadi Sambas
Keyword(s):  
Species Diversity ◽  
Tree Species ◽  
Human Activities ◽  
Diversity Index ◽  
Basal Area ◽  
Montane Forest ◽  
Tree Species Diversity ◽  
Importance Value ◽  
Montane Forests ◽  
Species Area

ADILI, A., KARTAWINATA, K., SOEDJITO, H. & SAMBAS, E. N. 2018. Tree species diversity in a pristine montane forest previously untouched by human activities in Foja Mountains, Papua, Indonesia. Reinwardtia 17(2): 133‒154. ‒‒ A study on structure and composition of the pristine montane forest previously untouched by human activities was conducted at the Foja Mountains in November 2008. We established a one-hectare plot divided into 100 subplots of 10 m × 10 m each. We enumerated all trees with DBH ≥ 10 cm which diameters were measured, heights were estimated and habitats were noted. We recorded 59 species, 42 genera and 27 families, comprising 693 trees with the total basal area (BA) of 41.35 m2/ha. The forest had lower species richness compared to those of lowland forests in Kalimantan, and Sumatra and montane forests in West Java. The Shannon-Wiener’s diversity index was 3.22. Nothofagus rubra (Importance Value, IV=47.89%) and Parinari corymbosa (IV=40.3%) were the dominant species, constituting the basis for designating the forest as the Nothofagus rubra - Parinari corymbosa association. To date, the dominance of N. rubra is unique to the Foja Mountains, as elsewhere in Papua the montane forests were dominated by N. pullei or other species. The species-area curve indicated a minimal area of 5000 m2. On the family level Fagaceae (IV=53.23%), Chrysobalanaceae (IV=40.53%) and Myristicaceae (IV=26.43%) were dominant. Verti-cally the forest consisted of four strata (A–D). In each stratum Nothofagus rubra, Platea latifolia, Parinari corymbosa and Myristica hollrungii were dominant. The diameter class distribution of Nothofagus rubra, Parinari corymbosa and Platea latifolia led us to assume that these species were regenerating well.

Species diversity in the Phanerozoic: species-area effects

Paleobiology ◽  
1976 ◽  
Vol 2 (4) ◽  
pp. 298-303 ◽  
Author(s):  
J. John Sepkoski
Keyword(s):  
Species Diversity ◽  
Multiple Regression ◽  
Fossil Species ◽  
Species Numbers ◽  
Habitat Area ◽  
Estimated Parameters ◽  
Total Correlation ◽  
Area Effects ◽  
Residual Variation ◽  
Species Area

Raup's (1976a) data on Phanerozoic species numbers are examined for species-area relationships, using published estimates of areas of continental seas. By means of multiple regression, species numbers are regressed on both estimated areas of seas and amounts of available rock for sampling, as measured by outcrop area and rock volume. Although the sampling effects apparently have the strongest influence on fossil species diversity, areas of seas substantially increase the total correlation, suggesting that Phanerozoic species numbers were in equilibrium with habitat area. This is further supported by the fact that estimated parameters in the regressions are fairly consistent with established island biogeographic theory. Much of the remaining residual variation can be explained by periods of disequilibrium.

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