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Sources of variation in extinction rates, turnover, and diversity of marine invertebrate families during the Paleozoic
We have recently shown how capture-recapture models can be used in conjunction with stratigraphic range data to estimate taxonomic extinction rates and taxonomic diversity. Here we present a new method that can be used to estimate taxonomic turnover (defined here as the proportion of taxa extant at time i , that originated in the interval i – 1 to i ). We used these methods in conjunction with stratigraphic range data for families in five phyla of Paleozoic marine invertebrates. We estimated fossil encounter probabilities, extinction rates, diversity, and turnover and used these estimates to test hypotheses about variation among phyla and geologic series. Encounter probabilities varied among taxa and showed evidence of a decrease over time for the geologic series examined. The number of families varied substantially among the five phyla and showed some evidence of an increase over the series examined. There was no evidence of variation in extinction probabilities among the phyla. Although there was evidence of temporal variation in extinction probabilities within phyla, there was no evidence of a linear decrease in extinction probabilities over time, as has been reported by others. We did find evidence of high extinction probabilities for the two intervals that had been identified by others as periods of mass extinction. We found no evidence of variation in turnover among the five phyla. There was evidence of temporal variation in turnover, with greater turnover occurring in the older series.
On the distribution of species occurrence
The distribution of species abundance (number of individuals per species) is well documented. The distribution of species occurrence (number of localities per species), however, has received little attention. This study investigates the distribution of species occurrence for five large data sets. For modern benthic foraminifera, species occurrence is examined from the Atlantic continental margin of North America, where 875 species were recorded 10,017 times at 542 localities, the Gulf of Mexico, where 848 species were recorded 18,007 times at 426 localities, and the Caribbean, where 1149 species were recorded 6684 times at 268 localities. For Late Cretaceous molluscs, species occurrence is examined from the Gulf Coast where 716 species were recorded 6236 times at 166 localities and a subset of this data consisting of 643 species recorded 3851 times at 86 localities. Logseries and lognormal distributions were fitted to these data sets. In most instances the logseries best predicts the distribution of species occurrence. The lognormal, however, also fits the data fairly well, and, in one instance, better. The use of these distributions allows the prediction of the number of species occurring once, twice, …, n times. Species abundance data are also available for the molluscan data sets. They indicate that the most abundant species (greatest number of individuals) usually occur most frequently. In all data sets approximately half the species occur four or less times. The probability of noting the presence of rarely occurring species is small, and, consequently, such species must be used with extreme caution in studies requiring knowledge of the distribution of species in space and time.
Alaskan Cretaceous-Tertiary floras and Arctic origins
Cretaceous floras in Alaska, when compared to those at mid-latitudes, generally indicate later appearances in Alaska of major clades and major leaf morphologies. Compared to mid-latitude floras , Alaskan Late Cretaceous floras contain few major clades. The Alaskan clades diversified but at a low taxonomic level. Migrational pathways into high latitudes were probably along streams. Similar patterns characterized the Alaskan Tertiary , although some southward migrations of lineages occurred during the Neogene. Review of other Arctic paleontological data from Ellesmere Island, previously used to suggest that the Arctic was a major center of origin during the Late Cretaceous , indicates that the ages of supposedly substantiating dinoflagellate floras were misinterpreted. When the dinoflagellate data are interpreted according to standard methodology, first occurrences of genera and species groups on Ellesmere are, like the Alaskan occurrences, later than first occurrences at middle latitudes.
Late Cretaceous-Cenozoic history of deciduousness and the terminal Cretaceous event.
Deciduousness in mesic, broad-leaved plants occurred in disturbed, middle-latitude environments during the Late Cretaceous. Only in polar environments in the Late Cretaceous was the deciduous element dominant, although of low diversity. The terminal Cretaceous event resulted in wide-spread selection for plants of deciduous habit and diversification of deciduous taxa, thus leaving a lasting imprint on Northern Hemisphere vegetation. Various environmental factors have played important roles in subsequent diversification of mesic, broad-leaved deciduous taxa and in origination and decline of broad-leaved deciduous forests. Low diversity and rarity of mesic deciduous plants in the post-Cretaceous of the Southern Hemisphere indicate that the inferred “impact winter” of the terminal Cretaceous event had little effect on Southern Hemisphere vegetation and climate.
Molluscan extinction patterns across the Cenomanian-Turonian Stage boundary in the western interior of the United States
High-resolution stratigraphic analysis of 18 sections spanning the Cenomanian–Turonian Stage boundary in the western interior of the United States has allowed determination of the magnitude and pattern of molluscan extinction and disruption. Composite range data from all sections show that the faunal turnover across the stage boundary occurs in a series of narrow stratigraphic zones, defined by multiple first and last occurrences, separated by intervals displaying little or no taxonomic turnover. Two of the apparent extinction steps (bottom and top of the Neocardioceras juddii Zone) may be intercontinentally developed. The additional steps apparently reflect cyclic changes in water mass and substrate characteristics in the western interior basin produced in response to orbital forcing of climate. An interval (ca. 10-100 k.y. duration) of changing community structure and general biotic deterioration is found below each of the two potentially intercontinentally developed extinction steps. The most affected mollusks were those having intercontinental distributions (ammonites and inoceramid bivalves), suggesting that disruption of planktotrophic larval dispersal may have played a role in increasing extinction and speciation rates near the C–T boundary. The nekto-benthic ammonites were affected earlier and to a greater degree than the pelagic forms, implying progressive upward expansion of the oxygen minimum zone preceding the stage boundary.
Predation, herbivory and kelp evolution
We propose that the kelps (Laminariales) radiated in the North Pacific following the onset of late Cenozoic polar cooling. The evidence is that (1) extant kelps occur exclusively in cold-water habitats; (2) all but one of 27 kelp genera occur in the North Pacific, 19 of these exclusively; and (3) limpets and herbivorous marine mammals obligately associated with kelps or other stipitate brown algae appeared late in the Cenozoic, even though more generalized forms of both groups are much older. We propose, further, that sea otters and perhaps other groups of benthic-feeding predatory mammals, whose late Cenozoic distributions all were limited to the North Pacific, created an environment for the evolution of kelps in which the intensity of herbivory was unusually low. We hypothesize that this interaction created predictable differences among habitats in the intensity of herbivory on several spatial scales, with resulting trade-offs between anti-herbivore defenses and plant competitive abilities in their respective floras. Sea otters incur time and energy costs for diving, resulting in depth-related reductions to foraging efficiency and thus increased sizes and densities of herbivorous sea urchins. Thus, the deep-water flora is well defended, but competitively subordinate, compared with the shallow-water flora. Similarly, we argue that during the same period of earth history, predation had less of a limiting influence on herbivorous invertebrates in the temperate southwestern Pacific. We hypothesize that (1) consequent biogeographical differences in the intensity of herbivory may have selected the phenolic-rich brown algal flora in temperate Australia/New Zealand; and (2) tightly coevolved plant/herbivore interactions may explain why Australian and New Zealand herbivores are undeterred by phenolics and why other classes of secondary compounds in the Australian/New Zealand flora significantly deter herbivores.
Evolution of large body size in abalones (Haliotis): Patterns and implications
Kelps and other fleshy macroalgae - dominant reef-inhabiting organisms in cool - seasmay have radiated extensively following late Cenozoic polar cooling, thus triggering a chain of evolutionary change in the trophic ecology of nearshore temperate ecosystems. We explore this hypothesis through an analysis of body size in the abalones (Gastropoda; Haliotidae), a widely distributed group in modern oceans that displays a broad range of body sizes and contains fossil representatives from the late Cretaceous (60-75 Ma). Geographic analysis of maximum shell length in living abalones showed that small-bodied species, while most common in the Tropics, have a cosmopolitan distribution, whereas large-bodied species occur exclusively in cold-water ecosystems dominated by kelps and other macroalgae. The phylogeography of body size evolution in extant abalones was assessed by constructing a molecular phylogeny in a mix of large and small species obtained from different regions of the world. This analysis demonstrates that small body size is the plesiomorphic state and largeness has likely arisen at least twice. Finally, we compiled data on shell length from the fossil record to determine how (slowly or suddenly) and when large body size arose in the abalones. These data indicate that large body size appears suddenly at the Miocene/Pliocene boundary. Our findings support the view that fleshy-algal dominated ecosystems radiated rapidly in the coastal oceans with the onset of the most recent glacial age. We conclude with a discussion of the broader implications of this change. ?? 2005 The Paleontological Society. All rights reserved.
Taphonomic and zooarchaeological implications of spotted hyena (crocuta crocuta) bone accumulations in kenya: A modern behavioral ecological approach
The significant impact of extant carnivores, particularly spotted hyenas, on the depo-sitional history and physical characteristics of archaeofaunal and paleontological assemblages is well recognized. We focus on the behavioral ecology of extant spotted hyenas (Crocuta crocuta) in relation to bone accumulations produced by one East African clan at communal dens. Limbs and skulls of prey animals more frequently appear at dens than do other carcass portions. These items reflect the relative abundance of prey species near dens; carnivore remains are poorly represented. Comparative analysis reveals that bones are deposited far more slowly (<7 carcass portions per month) and accumulations tend to be smaller at Crocuta dens than at dens of either brown (Para-hyaena brunnea) or striped (Hyaena hyaena) hyenas. We propose that extant Crocuta bone accumu-lation rates and sizes are likely affected by prey species abundance, clan size, social interactions within the clan, and the type and availability of den sites. We also suggest that the potential for intraspecific behavioral variability in bone accumulation patterns is important when comparisons are made among spotted hyena populations and across hyena species. For example, accumulation patterns may be dramatically influenced by the temporal span, potentially ranging from days to hundreds or thousands of years, in which bones are collected, depending on the species-specific history of occupation at a given site. Understanding the behavioral and ecological variability likely to influence bone accumulation patterns at dens used by different hyaenids will allow taphonomists and zooarchaeologists to refine their knowledge of mechanisms underlying site formation pro-cesses and potential causes of variability in deeper-time den assemblages. ?? 2009 The Paleontological Society.
Climatic forcing of Quaternary deep-sea benthic communities in the North Pacific Ocean
There is growing evidence that changes in deep-sea benthic ecosystems are modulated by climate changes, but most evidence to date comes from the North Atlantic Ocean. Here we analyze new ostracod and published foraminiferal records for the last 250,000 years on Shatsky Rise in the North Pacific Ocean. Using linear models, we evaluate statistically the ability of environmental drivers (temperature, productivity, and seasonality of productivity) to predict changes in faunal diversity, abundance, and composition. These microfossil data show glacial-interglacial shifts in overall abundances and species diversities that are low during glacial intervals and high during interglacials. These patterns replicate those previously documented in the North Atlantic Ocean, suggesting that the climatic forcing of the deep-sea ecosystem is widespread, and possibly global in nature. However, these results also reveal differences with prior studies that probably reflect the isolated nature of Shatsky Rise as a remote oceanic plateau. Ostracod assemblages on Shatsky Rise are highly endemic but of low diversity, consistent with the limited dispersal potential of these animals. Benthic foraminifera, by contrast, have much greater dispersal ability and their assemblages at Shatsky Rise show diversities typical for deep-sea faunas in other regions. Statistical analyses also reveal ostracod-foraminferal differences in relationships between environmental drivers and biotic change. Rarefied diversity is best explained as a hump-shaped function of surface productivity in ostracods, but as having a weak and positive relationship with temperature in foraminifera. Abundance shows a positive relationship with both productivity and seasonality of productivity in foraminifera, and a hump-shaped relationship with productivity in ostracods. Finally, species composition in ostracods is influenced by both temperature and productivity, but only a temperature effect is evident in foraminifera. Though complex in detail, the global-scale link between deep-sea ecosystems and Quaternary climate changes underscores the importance of the interaction between the physical and biological components of paleoceanographical research for better understanding the history of the biosphere.
Ecological and evolutionary consequences of benthic community stasis in the very deep sea (>1500 m)
An enigma of deep-sea biodiversity research is that the abyss with its low productivity and densities appears to have a biodiversity similar to that of shallower depths. This conceptualization of similarity is based mainly on per-sample estimates (point diversity, within-habitat, or α-diversity). Here, we use a measure of between-sample within-community diversity (β 1H ) to examine benthic foraminiferal diversity between 333 stations within 49 communties from New Zealand, the South Atlantic, the Gulf of Mexico, the Norwegian Sea, and the Arctic. The communities are grouped into two depth categories: 200–1500 m and >1500 m. β 1H diversity exhibits no evidence of regional differences. Instead, higher values at shallower depths are observed worldwide. At depths of >1500 m the average β 1H is zero, indicating stasis or no biodiversity gradient. The difference in β 1H -diversity explains why, despite species richness often being greater per sample at deeper depths, the total number of species is greater at shallower depths. The greater number of communities and higher rate of evolution resulting in shorter species durations at shallower depths is also consistent with higher β 1H values.
Postcards from the field
My research focuses on pre-20th century conditions in the Greater Everglades Ecosystem of south Florida to provide the context for resource managers to set targets for restoration. A primary goal of Everglades restoration is to re-establish more natural delivery of freshwater to the wetlands and estuaries in the region. By analyzing biotic assemblages from sediment cores collected from Florida Bay and Biscayne Bay, we can estimate pre-water management salinities and freshwater flow. To interpret the environments represented by the core assemblages, we investigate the environmental requirements of the living organisms. Our recent efforts have focused on the mangrove transition zone and after a pandemic-related hiatus, we were ecstatic to get back in the field in August 2021! Here, I am searching for mollusks and other invertebrates at the base of dwarf mangroves, near Whitewater Bay, Everglades National Park.