The causes of extinction

A species may go extinct either because it is unable to evolve rapidly enough to meet changing circumstances, or because its niche disappears and no capacity for rapid evolution could have saved it. Although recent extinctions can usually be interpreted as resulting from niche disappearance, the taxonomic distribution of parthenogens suggests that inability to evolve may also be important. A second distinction is between physical and biotic causes of extinction. Fossil evidence for constant taxonomic diversity, combined with species turnover, implies that biotic factors have been important. A similar conclusion emerges from studies of recent introductions of predators, competitors and parasites into new areas. The term ‘species selection’ should be confined to cases in which the outcome of selection is determined by properties of the population as a whole, rather than of individuals. The process has been of only trivial importance in producing complex adaptations, but of major importance in determining the distribution of different types of organisms. An adequate interpretation of the fossil record requires a theory of the coevolution of many interacting species. Such a theory is at present lacking, but various approaches to it are discussed.

Author(s):  
Mauro Gobbi ◽  
Valeria Lencioni

Carabid beetles and chironomid midges are two dominant cold-adapted taxa, respectively on glacier forefiel terrains and in glacial-stream rivers. Although their sensitivity to high altitude climate warming is well known, no studies compare the species assemblages exhibited in glacial systems. Our study compares diversity and distributional patterns of carabids and chironomids in the foreland of the receding Amola glacier in central-eastern Italian Alps. Carabids were sampled by pitfall traps; chironomids by kick sampling in sites located at the same distance from the glacier as the terrestrial ones. The distance from the glacier front was considered as a proxy for time since deglaciation since these variables are positively correlated. We tested if the distance from the glacier front affects: i) the species richness; ii) taxonomic diversity; and iii) species turnover. Carabid species richness and taxonomic diversity increased positively from recently deglaciated sites (those c. 160 m from the glacier front) to sites deglaciated more than 160yrs ago (those located >1300 m from glacier front). Species distributions along the glacier foreland were characterized by mutually exclusive species. Conversely, no pattern in chironomid species richness and turnover was observed. Interestingly, taxonomic diversity increased significantly: closely related species were found near the glacier front, while the most taxonomically diverse species assemblages were found distant from the glacier front. Increasing glacial retreat differently affect epigeic and aquatic insect taxa: carabids respond faster to glacier retreat than do chironomids, at least in species richness and species turnover patterns.


Palaios ◽  
2021 ◽  
Vol 36 (3) ◽  
pp. 115-121
Author(s):  
EDUARDO MAYORAL ◽  
JORGE F. GENISE ◽  
FRANCISCO J. RODRÍGUEZ-TOVAR ◽  
ANA SANTOS

ABSTRACT Plio?-Pleistocene outcrops located at the southwestern edge of the Guadalquivir Basin in the area of Lepe (Huelva, Spain) provide an interesting example for studying the contemporaneity of traces with the rocks that contain them. Two different types of cells compatible with the ichnogenera Celliforma (Type 1) and Palmiraichnus (Type 2) were found in these outcrops. Their walls were constructed with the same material as the matrix and our first research in the area showed no extant bees producing them suggesting that they were coeval with the trace-bearing rocks. The case of the “Palmiraichnus-like” Type 2 cells was misleading because of its similarity with Palmiraichnus described from the region in the Canary Islands and Balearic Archipelago (Spain). Two determining features were vital in clarifying this first appearance. In the Palmiraichnus-like cells we found remains of a larval cocoon in one cell that could be dated by C14, giving a modern age. In the Celliforma-like cells more field research in the area allow us to observe extant bees nesting in these rocks in autumn. Ichnological literature show a few cases of asynchronies involving extant traces found mostly in Paleozoic and Mesozoic rocks. In contrast, the case presented herein indicates the time gap between the bearing rocks and the Lepe traces was shorter (ca. 12 ky–2.6 My), enhancing the similarity of traces and rocks and thus their potential coevalness. This case may serve as a warning about other potential examples in the fossil record in which relatively short asynchronies between traces and paleosols exist.


2006 ◽  
Vol 29 (1) ◽  
pp. 55-80
Author(s):  
Jere H Lipps

The major features of protist evolution are fraught with controversies, problems and few answers, especially in early Earth history. In general they are based on molecular data and fossil evidence that respectively provide a scaffold and details of eukaryotic phylogenetic and ecologic histories. 1. Their origin, inferred from molecular sequences, occurred very early (>;3Ga). They are a chimera of different symbiont-derived organelles, including possibly the nucleus. 2. The initial diversification of eukaryotes may have occurred early in geologic time. Six supergroups exist today, each with fossils known from the Proterozoic and Phanerozoic. 3. Sex, considered an important development, may have been inherited from bacteria. 4. Precambrian protists were largely pelagic cyst-bearing taxa, but benthic forms were probably quite diverse and abundant. 5. Protists gave rise to animals long before 600 Ma through the choanoflagellates, for which no fossil record exists. 6. Acritarchs and skeletonized protists radiated in the Cambrian (544-530 my). From then on, they radiated and became extinct at all the major events recorded in the metazoan fossil record. 7. Protists dominated major environments (shelves and reefs) starting with a significant radiation in the Ordovician, followed by extinctions and other radiations until most died out at the end of the Permian. 8. In the Mesozoic, new planktic protozoa and algae appeared and radiated in pelagic environments. 9. Modern protists are important at all trophic levels in the oceans and a huge number terrestrial, parasitic and symbiotic protists must have existed for much of geologic time as well. 10. The future of protists is likely in jeopardy, just like most reefal, benthic, and planktic metazoans. An urgent need to understand the role of protists in modern threatened oceans should be addressed soon.


2019 ◽  
Vol 189 (2) ◽  
pp. 635-656 ◽  
Author(s):  
Ane De Celis ◽  
Iván Narváez ◽  
Francisco Ortega

Abstract Eusuchia is a crocodyliform clade with a rich and diverse fossil record dating back to the Mesozoic. There are several recent studies that analyse crocodyliform palaeodiversity over time, but none of them focuses exclusively on eusuchians. Thus, we estimated subsampled eusuchian palaeodiversity species dynamics over time not only at a global scale, but also by continents and main crocodylian lineages (Alligatoroidea, Crocodyloidea and Gavialoidea). These estimates reveal complex spatiotemporal palaeodiversity patterns, in which two maxima can be detected: the first during the Palaeocene and the second, which is also the biggest, in the middle-late Miocene. The Palaeocene shift is related to a North American alligatoroid diversification, whereas the middle–late Miocene maximum is related to a diversification of the three main Crocodylia lineages in Gondwanan land masses, but especially in South America. Additionally, a model-based study using generalized least squares was carried out to analyse the relationships between different abiotic and sampling proxies and eusuchian palaeodiversity. The results show that palaeotemperature is the most important factor amongst the analysed proxies, in accordance with previous studies. However, the results suggest that, along with palaeotemperature, other abiotic and/or biotic factors might also be driving eusuchian palaeodiversity dynamics.


2020 ◽  
Vol 287 (1928) ◽  
pp. 20200652
Author(s):  
Johannes Cairns ◽  
Felix Moerman ◽  
Emanuel A. Fronhofer ◽  
Florian Altermatt ◽  
Teppo Hiltunen

Predator–prey interactions heavily influence the dynamics of many ecosystems. An increasing body of evidence suggests that rapid evolution and coevolution can alter these interactions, with important ecological implications, by acting on traits determining fitness, including reproduction, anti-predatory defence and foraging efficiency. However, most studies to date have focused only on evolution in the prey species, and the predator traits in (co)evolving systems remain poorly understood. Here, we investigated changes in predator traits after approximately 600 generations in a predator–prey (ciliate–bacteria) evolutionary experiment. Predators independently evolved on seven different prey species, allowing generalization of the predator's evolutionary response. We used highly resolved automated image analysis to quantify changes in predator life history, morphology and behaviour. Consistent with previous studies, we found that prey evolution impaired growth of the predator, although the effect depended on the prey species. By contrast, predator evolution did not cause a clear increase in predator growth when feeding on ancestral prey. However, predator evolution affected morphology and behaviour, increasing size, speed and directionality of movement, which have all been linked to higher prey search efficiency. These results show that in (co)evolving systems, predator adaptation can occur in traits relevant to foraging efficiency without translating into an increased ability of the predator to grow on the ancestral prey type.


1992 ◽  
Vol 6 ◽  
pp. 174-174 ◽  
Author(s):  
Conrad C. Labandeira

A considerable amount of research has been devoted toward evaluating the impact of the Cretaceous/Tertiary extinction on terrestrial life. This research has focused primarily on terrestrial vertebrates (primarily dinosaurs), marine invertebrates (notably molluscs and foraminifera), and to a lesser extent, terrestrial vascular plants. Terrestrial arthropods, especially insects, have seldomly been investigated, principally because of an alleged depauperate fossil record. Nevertheless, within the past two decades, some of the most productive and taxonomically diverse insect faunas have originated from Cretaceous amber- and compression-fossil deposits from every continent. Whereas it was once thought that the Cretaceous represented an unknown void in the understanding of insect evolution, now it appears that many extant lineages are traceable to Cretaceous precursors.Three approaches are available for determining the extent of the effect of the terminal Cretaceous extinction event on insects. Assessed for the interval from the Early Cretaceous to the Early Paleogene, these approaches are: (1) establishing the secular pattern of familial- and generic-based taxonomic diversity (macroevolution); (2) recognizing the persistence or eradication of specific insect/vascular plant interactions, such as leaf-mining, wood-boring and pollination (behavior); and (3) establishing temporal trends in the range of mouthpart design, as an indicator of faunal disparity or structural diversity (morphology). These three operationally separate but complimentary approaches allow the advantage of using distinct data bases to bear on a common question. The body-fossil record of insects provides primary data for the taxonomic expansion, steady-state, or contraction of insect faunas. The trace-fossil record of those insect interactions that are coevolved with plant hosts reveals the temporal continuity of highly stereotyped and taxonomically obligate behaviors. Both of these are contrasted to an assessment of insectan structural disparity, herein determined from a robust data base of 30 modern insect mouthpart classes that are traced back in geologic time.A preliminary analysis of each of these three approaches indicates broad agreement–namely that insects were not dramatically affected by the terminal Cretaceous extinction event. First, insects experienced only a modest decline in diversity, about 9 percent at the family level. (The generic level is not yet analyzed.) Second, although the data base is limited, there is no indication of the extinction of major leaf-mining, wood-boring, pollinating or other plant-specific behaviors at the end of the Cretaceous. In fact, leaf-mine morphologies for three lepidopteran families with Cretaceous occurrences are apparently indistinguishable from their modern descendants. Last, of the 30 mouthpart classes occurring during the Paleogene, 28 are represented during the Cretaceous. These data provide strong evidence for a largely uninterrupted continuum of insect faunas across the Cretaceous/Tertiary boundary as measured by taxonomic diversity, coevolved behavior, and structural disparity.Because of abundant and often intimate associations between insects and flowering plants, these results are consistent with a gradual and not catastrophic change in terrestrial floras across the Cretaceous/Tertiary boundary. Acceptance of a catastrophic extinction of flowering plants during the terminal Cretaceous would necessitate an unprecedented level of host-switching by coevolved insects on contemporaneous plants. This is unlikely, based on evidence from the prolific literature on modern insect/plant interactions. These studies indicate the ubiquity of obligate insect specificity for various secondary chemicals on many flowering plant species.


2011 ◽  
Vol 279 (1732) ◽  
pp. 1300-1309 ◽  
Author(s):  
Rampal S. Etienne ◽  
Bart Haegeman ◽  
Tanja Stadler ◽  
Tracy Aze ◽  
Paul N. Pearson ◽  
...  

The branching times of molecular phylogenies allow us to infer speciation and extinction dynamics even when fossils are absent. Troublingly, phylogenetic approaches usually return estimates of zero extinction, conflicting with fossil evidence. Phylogenies and fossils do agree, however, that there are often limits to diversity. Here, we present a general approach to evaluate the likelihood of a phylogeny under a model that accommodates diversity-dependence and extinction. We find, by likelihood maximization, that extinction is estimated most precisely if the rate of increase in the number of lineages in the phylogeny saturates towards the present or first decreases and then increases. We demonstrate the utility and limits of our approach by applying it to the phylogenies for two cases where a fossil record exists (Cetacea and Cenozoic macroperforate planktonic foraminifera) and to three radiations lacking fossil evidence ( Dendroica , Plethodon and Heliconius ). We propose that the diversity-dependence model with extinction be used as the standard model for macro-evolutionary dynamics because of its biological realism and flexibility.


2015 ◽  
Vol 370 (1684) ◽  
pp. 20150038 ◽  
Author(s):  
Gregory D. Edgecombe ◽  
Xiaoya Ma ◽  
Nicholas J. Strausfeld

Extant panarthropods (euarthropods, onychophorans and tardigrades) are hallmarked by stunning morphological and taxonomic diversity, but their central nervous systems (CNS) are relatively conserved. The timing of divergences of the ground pattern CNS organization of the major panarthropod clades has been poorly constrained because of a scarcity of data from their early fossil record. Although the CNS has been documented in three-dimensional detail in insects from Cenozoic ambers, it is widely assumed that these tissues are too prone to decay to withstand other styles of fossilization or geologically older preservation. However, Cambrian Burgess Shale-type compressions have emerged as sources of fossilized brains and nerve cords. CNS in these Cambrian fossils are preserved as carbon films or as iron oxides/hydroxides after pyrite in association with carbon. Experiments with carcasses compacted in fine-grained sediment depict preservation of neural tissue for a more prolonged temporal window than anticipated by decay experiments in other media. CNS and compound eye characters in exceptionally preserved Cambrian fossils predict divergences of the mandibulate and chelicerate ground patterns by Cambrian Stage 3 ( ca 518 Ma), a dating that is compatible with molecular estimates for these splits.


2006 ◽  
Vol 361 (1470) ◽  
pp. 887-902 ◽  
Author(s):  
Martin Brasier ◽  
Nicola McLoughlin ◽  
Owen Green ◽  
David Wacey

The rock record provides us with unique evidence for testing models as to when and where cellular life first appeared on Earth. Its study, however, requires caution. The biogenicity of stromatolites and ‘microfossils’ older than 3.0 Gyr should not be accepted without critical analysis of morphospace and context, using multiple modern techniques, plus rejection of alternative non-biological (null) hypotheses. The previous view that the co-occurrence of biology-like morphology and carbonaceous chemistry in ancient, microfossil-like objects is a presumptive indicator of biogenicity is not enough. As with the famous Martian microfossils, we need to ask not ‘what do these structures remind us of?’, but ‘what are these structures?’ Earth's oldest putative ‘microfossil’ assemblages within 3.4–3.5 Gyr carbonaceous cherts, such as the Apex Chert, are likewise self-organizing structures that do not pass tests for biogenicity. There is a preservational paradox in the fossil record prior to ca 2.7 Gyr: suitable rocks (e.g. isotopically light carbonaceous cherts) are widely present, but signals of life are enigmatic and hard to decipher. One new approach includes detailed mapping of well-preserved sandstone grains in the ca 3.4 Gyr Strelley Pool Chert. These can contain endolithic microtubes showing syngenicity, grain selectivity and several levels of geochemical processing. Preliminary studies invite comparison with a class of ambient inclusion trails of putative microbial origin and with the activities of modern anaerobic proteobacteria and volcanic glass euendoliths.


Paleobiology ◽  
1975 ◽  
Vol 1 (4) ◽  
pp. 333-342 ◽  
Author(s):  
David M. Raup

Benthic ecologists have successfully applied rarefaction techniques to the problem of compensating for the effect of sample size on apparent species diversity (= species richness). The same method can be used in studies of diversity at higher taxonomic levels (families and orders) in the fossil record where samples represent world-wide distributions of species or genera over long periods of geologic time.Application of rarefaction to several large samples of post-Paleozoic echinoids (totaling 7,911 species) confirms the utility of the method. Rarefaction shows that the observed increase in the number of echinoid families since the Paleozoic is real in the sense that it cannot be explained solely by the increase in numbers of preserved species. There has been no statistically significant increase in the number of families since mid-Cretaceous, however. At the order level, echinoid diversity may have been nearly constant since late Triassic or early Jurassic.


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