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  1. Ecosystem structure—that is the species present, the functions they represent, and how those functions interact—is an important determinant of community stability. This in turn affects how ecosystems respond to natural and anthropogenic crises, and whether species or the ecological functions that they represent are able to persist. Here we use fossil data from museum collections, literature, and the Paleobiology Database to reconstruct trophic networks of Tethyan paleocommunities from the Anisian and Carnian (Triassic), Bathonian (Jurassic), and Aptian (Cretaceous) stages, and compare these to a previously reconstructed trophic network from a modern Jamaican reef community. We generated model food webs consistent with functional structure and taxon richnesses of communities, and compared distributions of guild level parameters among communities, to assess the effect of the Mesozoic Marine Revolution on ecosystem dynamics. We found that the trophic space of communities expanded from the Anisian to the Aptian, but this pattern was not monotonic. We also found that trophic position for a given guild was subject to variation depending on what other guilds were present in that stage. The Bathonian showed the lowest degree of trophic omnivory by top consumers among all Mesozoic networks, and was dominated by longer food chains. In contrast, the Aptian network displayed a greater degree of short food chains and trophic omnivory that we attribute to the presence of large predatory guilds, such as sharks and bony fish. Interestingly, the modern Jamaican community appeared to have a higher proportion of long chains, as was the case in the Bathonian. Overall, results indicate that trophic structure is highly dependent on the taxa and ecological functions present, primary production experienced by the community, and activity of top consumers. Results from this study point to a need to better understand trophic position when planning restoration activities because a community may be so altered by human activity that restoring a species or its interactions may no longer be possible, and alternatives must be considered to restore an important function. Further work may also focus on elucidating the precise roles of top consumers in moderating network structure and community stability. 
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  3. Stratigraphic sections in the Bogda Mountains, NW China, provide detailed records of late Permian–Early Triassic terrestrial paleoenvironmental and paleoclimatic evolution at the paleo-mid-latitude of NE Pangea. The sections are located in the Tarlong-Taodonggou, Dalongkou, and Zhaobishan areas, ~100 km apart, and ~5000 m in total thickness. An age model was constructed using seven high-resolution U-Pb zircon CA-TIMS dates in the Tarlong-Taodonggou sections and projected to sections in two other areas to convert the litho- and cyclo-stratigraphy into a chronostratigraphy. Sediments were deposited in braided and meandering streams, and lacustrine deltaic and lakeplain-littoral environments. A cyclostratigraphy was established on the basis of repetitive environmental changes for high-order cycles, stacking patterns of high-order cycles, and long-term climatic and tectonic trends for low-order cycles (LC). Sedimentary evidence from the upper Wuchiapingian–mid Induan Wutonggou LC indicates that the climate was generally humid-subhumid and gradually became variable toward a seasonally dry condition in the early Induan. Lush vegetation had persisted across the Permo–Triassic boundary into the early Induan. A subhumid-semiarid condition prevailed during the deposition of mid Induan–lower Olenekian Jiucaiyuan and lower Olenekian Shaofanggou LCs. These three LCs are largely continuous and separated by conformities and diastems. Intra- and inter-graben stratigraphic variability is reflected by variations in thickness, depositional system, and average sedimentation rate, and results in variable spatial and temporal stratigraphic resolution. Such stratigraphic variability is mainly controlled by paleogeographic location, depocenter shift, and episodic uplift and subsidence in the source areas and catchment basin. A changeover of plant communities occurred during the early Induan, postdating the end-Permian marine mass extinction. However, riparian vegetation and upland forests were still present from the mid Induan to early Olenekian, and served as primary food source for terrestrial ecosystems, including vertebrates. Correlation of the vascular plant evolutionary history from the latest Changhsingian to early Induan in the Bogda Mountains with those reported from Australia and south China indicates a diachronous floral changeover on Pangea. The late Permian–Early Triassic litho-, cyclo- and chrono-stratigraphies, constrained by the age model, providesfoundation for future studies on the evolution of continental sedimentary, climatic, biologic, and ecological systems in the Bogda region. It also provides a means to correlate terrestrial events in the mid-paleolatitudes with marine and nonmarine records in the other parts of the world. 
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    The Earth has been beset by many crises during its history, and yet comparing the ecological impacts of these mass extinctions has been difficult. Key questions concern the kinds of species that go extinct and survive, how communities rebuild in the post-extinction recovery phase, and especially how the scaling of events affects these processes. Here, we explore ecological impacts of terrestrial and freshwater ecosystems in three mass extinctions through the mid-Phanerozoic, a span of 121 million years (295–174 Ma). This critical duration encompasses the largest mass extinction of all time, the Permian–Triassic (P–Tr) and is flanked by two smaller crises, the Guadalupian–Lopingian (G–L) and Triassic–Jurassic (T–J) mass extinctions. Palaeocommunity dynamics modelling of 14 terrestrial and freshwater communities through a long sedimentary succession from the lower Permian to the lower Jurassic in northern Xinjiang, northwest China, shows that the P–Tr mass extinction differed from the other two in two ways: (i) ecological recovery from this extinction was prolonged and the three post-extinction communities in the Early Triassic showed low stability and highly variable and unpredictable responses to perturbation primarily following the huge losses of species, guilds and trophic space; and (ii) the G–L and T–J extinctions were each preceded by low-stability communities, but post-extinction recovery was rapid. Our results confirm the uniqueness of the P–Tr mass extinction and shed light on the trophic structure and ecological dynamics of terrestrial and freshwater ecosystems across the three mid-Phanerozoic extinctions, and how complex communities respond to environmental stress and how communities recovered after the crisis. Comparisons with the coeval communities from the Karoo Basin, South Africa show that geographically and compositionally different communities of terrestrial ecosystems were affected in much the same way by the P–Tr extinction. 
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  5. A thorough understanding of how communities respond to extreme changes, such as biotic invasions, is essential to manage ecosystems today. Here we constructed fossil food webs to identify changes in Late Ordovician (Katian) shallow-marine paleocommunity structure and functioning before and after the Richmondian invasion, a well-documented ancient invasion. Food webs were compared using descriptive metrics and cascading extinction on graphs models. Richness at intermediate trophic levels was underrepresented when using only data from the Paleobiology Database relative to museum collections, resulting in a spurious decrease in modeled paleocommunity stability. Therefore, museum collections and field sampling may provide more reliable sources of data for the reconstruction of trophic organization in comparison to online data repositories. The invasion resulted in several changes in ecosystem dynamics. Despite topological similarities between pre- and postinvasion food webs, species loss occurred corresponding to a minor decrease in functional groups. Invaders occupied all of the preinvasion functional guilds, with the exception of four incumbent guilds that were lost and one new guild, corroborating the notion that invaders replace incumbents and fill preexisting niche space. Overall, models exhibited strong resistance to secondary extinction, although the postinvasion community had a lower threshold of collapse and more variable response to perturbation. We interpret these changes in dynamics as a decrease in stability, despite similarities in overall structure. Changes in food web structure and functioning resulting from the invasion suggest that conservation efforts may need to focus on preserving functional diversity if more diverse ecosystems are not inherently more stable. 
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  6. Abstract. Microfossil assemblages provide valuable records to investigatevariability in continental margin biogeochemical cycles, including dynamicsof the oxygen minimum zone (OMZ). Analyses of modern assemblages acrossenvironmental gradients are necessary to understand relationships betweenassemblage characteristics and environmental factors. Five cores wereanalyzed from the San Diego margin (32∘42′00′′ N, 117∘30′00′′ W; 300–1175 m water depth) for core top benthic foraminiferalassemblages to understand relationships between community assemblages andspatial hydrographic gradients as well as for down-core benthic foraminiferalassemblages to identify changes in the OMZ through time. Comparisons ofbenthic foraminiferal assemblages from two size fractions (63–150 and>150 µm) exhibit similar trends across the spatial and environmental gradient or in some cases exhibit more pronouncedspatial trends in the >150 µm fraction. A range of speciesdiversity exists within the modern OMZ (1.910–2.586 H, Shannon index),suggesting that diversity is not driven by oxygenation alone. We identifytwo hypoxic-associated species (B. spissa and U. peregrina), one oxic-associated species (G. subglobosa) andone OMZ edge-associated species (B. argentea). Down-core analysis of indicator speciesreveals variability in the upper margin of the OMZ (528 m water depth) whilethe core of the OMZ (800 m) and below the OMZ (1175 m) remained stable inthe last 1.5 kyr. We document expansion of the upper margin of the OMZbeginning 400 BP on the San Diego margin that is synchronous with otherregional records of oxygenation. 
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  7. Abstract

    In the face of ongoing marine deoxygenation, understanding timescales and drivers of past oxygenation change is of critical importance. Marine sediment cores from tiered silled basins provide a natural laboratory to constrain timing and implications of oxygenation changes across multiple depths. Here, we reconstruct oxygenation and environmental change over time using benthic foraminiferal assemblages from sediment cores from three basins across the Southern California Borderlands: Tanner Basin (EW9504‐09PC, 1,194 m water depth), San Nicolas Basin (EW9504‐08PC, 1,442 m), and San Clemente Basin (EW9504‐05PC,1,818 m). We utilize indicator taxa, community ecology, and an oxygenation transfer function to reconstruct past oxygenation, and we directly compare reconstructed dissolved oxygen to modern measured dissolved oxygen. We generate new, higher resolution carbon and oxygen isotope records from planktic (Globigerina bulloides) and benthic foraminifera (Cibicides mckannai) from Tanner Basin. Geochemical and assemblage data indicate limited ecological and environmental change through time in each basin across the intervals studied. Early to mid‐Holocene (11.0–4.7 ka) oxygenation below 1,400 m (San Clemente and San Nicolas) was relatively stable and reduced relative to modern. San Nicolas Basin experienced a multi‐centennial oxygenation episode from 4.7 to 4.3 ka and oxygenation increased in Tanner Basin gradually from 1.7 to 0.8 ka. Yet across all three depths and time intervals studied, dissolved oxygen is consistently within a range of intermediate hypoxia (0.5–1.5 ml L−1[O2]). Variance in reconstructed dissolved oxygen was similar to decadal variance in modern dissolved oxygen and reduced relative to Holocene‐scale changes in shallower basins.

     
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