scholarly journals Diversity, diets and disparity: determining the effect of the terminal Cretaceous extinction on insect evolution

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.

Author(s):  
Sandra R Schachat ◽  
Conrad C Labandeira

Abstract Time and again, over hundreds of millions of years, environmental disturbances have caused mass extinctions of animals ranging from reptiles to corals. The anthropogenic loss of species diversity happening now is often discussed as the ‘sixth mass extinction’ in light of the ‘Big Five’ mass extinctions in the fossil record. But insects, whose taxonomic diversity now appears to be threatened by human activity, have a unique extinction history. Prehistoric losses of insect diversity at the levels of order and family appear to have been driven by competition among insect lineages, with biotic replacement ensuring minimal net losses in taxonomic diversity. The end-Permian extinction, the ‘mother of mass extinctions’ in the seas, was more of a faunal turnover than a mass extinction for insects. Insects’ current biotic crisis has been measured in terms of the loss of abundance and biomass (rather than the loss of species, genera, or families) and these are essentially impossible to measure in the fossil record. However, should the ongoing loss of insect abundance and biomass cause the demise of many insect families, the current extinction event may well be the first sudden loss of higher-level insect diversity in our planet’s history. This is not insects’ sixth mass extinction—in fact, it may become their first.


2016 ◽  
Vol 283 (1832) ◽  
pp. 20160256 ◽  
Author(s):  
David M. Grossnickle ◽  
Elis Newham

It is often postulated that mammalian diversity was suppressed during the Mesozoic Era and increased rapidly after the Cretaceous–Palaeogene (K–Pg) extinction event. We test this hypothesis by examining macroevolutionary patterns in early therian mammals, the group that gave rise to modern placentals and marsupials. We assess morphological disparity and dietary trends using morphometric analyses of lower molars, and we evaluate generic level taxonomic diversity patterns using techniques that account for sampling biases. In contrast with the suppression hypothesis, our results suggest that an ecomorphological diversification of therians began 10–20 Myr prior to the K–Pg extinction event, led by disparate metatherians and Eurasian faunas. This diversification is concurrent with ecomorphological radiations of multituberculate mammals and flowering plants, suggesting that mammals as a whole benefitted from the ecological rise of angiosperms. In further contrast with the suppression hypothesis, therian disparity decreased immediately after the K–Pg boundary, probably due to selective extinction against ecological specialists and metatherians. However, taxonomic diversity trends appear to have been decoupled from disparity patterns, remaining low in the Cretaceous and substantially increasing immediately after the K–Pg extinction event. The conflicting diversity and disparity patterns suggest that earliest Palaeocene extinction survivors, especially eutherian dietary generalists, underwent rapid taxonomic diversification without considerable morphological diversification.


Author(s):  
Stefan A. Rensing ◽  
Dolf Weijers

AbstractThe seeds of flowering plants are sexually produced propagules that ensure dispersal and resilience of the next generation. Seeds harbor embryos, three dimensional structures that are often miniatures of the adult plant in terms of general structure and primordial organs. In addition, embryos contain the meristems that give rise to post-embryonically generated structures. However common, flowering plant embryos are an evolutionary derived state. Flowering plants are part of a much larger group of embryo-bearing plants, aptly termed Embryophyta. A key question is what evolutionary trajectory led to the emergence of flowering plant embryos. In this opinion, we deconstruct the flowering plant embryo and describe the current state of knowledge of embryos in other plant lineages. While we are far yet from understanding the ancestral state of plant embryogenesis, we argue what current knowledge may suggest and how the knowledge gaps may be closed.


2016 ◽  
Vol 8 (1) ◽  
pp. 42 ◽  
Author(s):  
Bridget O. Bobadoye ◽  
Paul N. Ndegwa ◽  
Lucy Irungu ◽  
Fombong Ayuka ◽  
Robert Kajobe

A vast majority of insects visit flowers for food, generally termed as floral rewards. Detailed insights on flowering phenology of plants could give a hint of habitat status and the extent to which such landscapes could support insect pollinators to render both direct and indirect ecosystem services. This study monitored flowering plants which could potentially provide both pollen and nectar sources to four African meliponine bee species (Apidae: Meliponini) naturally occurring in six diverse habitat gradients of the eastern arc mountains (Taita hills) of Kenya. Blooming sequences of identified flowering plants overlapped across seasons with approximately 80 different plant species belonging to 34 families recorded, with the highest proportions from Fabaceae and Asteraceae families dominating flowering plants that were visited (67% of the visits).  A flowering calendar is presented to indicate the phenological pattern of all identified floral resources.  Hypotrigona gribodoi being the most abundant species had the highest visitation rates on plants belonging to Fabaceae and Asteraceae families, followed by Meliponula ferruginea (black), Plebeina hildebrandti and Hypotrigona ruspolii. This indicates that such fragile habitat could invariably sustain nutritional requirements essential for the survival of insect pollinators such as native meliponine bee species, though bee abundance at flowers did not significantly correlate to food availability (expressed by flowering plant richness).


2017 ◽  
Author(s):  
Ryan Rayl ◽  
Stephen Wratten

Historically, handling insects has usually involved their being killed, but non-lethal approaches are necessary when evaluating the biology of such organisms. Anesthesia has been used as one of these non-lethal approaches. Two common anesthetics used in this way have been carbon dioxide and chilling. These have been used frequently in the literature but have sub-lethal effects on insects that may affect further experimentation. An alternative anesthetic that has potential for experimental use is triethylamine (TEA). This shows promise because of its ease of use and potency as an insect anesthetic, but evidence, if any, of the sub-lethal effects is almost non-existent in the literature. Here, longevity was use as a proxy for fitness as this is a common approach to laboratory work of this type for pests and their natural enemies. A series of experiments were carried out to find the optimal rates for these three selected anesthetics. The organism selected for this work was the fly Scaptomyza flava (Fallén), the larvae of which mine the leaves of commercial brassica crops worldwide. It is a ‘cosmetic’ pest in that damage thresholds for crop rejection are very low and prophylactic use of insecticides is the norm. One way of mitigating the negative environmental aspects of this approach is to enhance biological control. One such way of enhancing biological control is the use of flowering plants, as they can provide alternative resources to natural enemies, which can enhance their ability to control pests. To evaluate these flowering plants, handling of the insects is necessary and anesthesia is used for this purpose. For each anesthetic an optimal rate was found, then these rates were compared to each other in a subsequent experiment. These anesthetics differed markedly in their value in terms of the duration of the anesthesia and other practical considerations. TEA had the longest effect, CO2 and chilling had the shortest. All three were similar in their effects on longevity (i.e. recovery time and mortality rates).


2021 ◽  
Author(s):  
William J. Baker ◽  
Paul Bailey ◽  
Vanessa Barber ◽  
Abigail Barker ◽  
Sidonie Bellot ◽  
...  

AbstractThe tree of life is the fundamental biological roadmap for navigating the evolution and properties of life on Earth, and yet remains largely unknown. Even angiosperms (flowering plants) are fraught with data gaps, despite their critical role in sustaining terrestrial life. Today, high-throughput sequencing promises to significantly deepen our understanding of evolutionary relationships. Here, we describe a comprehensive phylogenomic platform for exploring the angiosperm tree of life, comprising a set of open tools and data based on the 353 nuclear genes targeted by the universal Angiosperms353 sequence capture probes. This paper (i) documents our methods, (ii) describes our first data release and (iii) presents a novel open data portal, the Kew Tree of Life Explorer (https://treeoflife.kew.org). We aim to generate novel target sequence capture data for all genera of flowering plants, exploiting natural history collections such as herbarium specimens, and augment it with mined public data. Our first data release, described here, is the most extensive nuclear phylogenomic dataset for angiosperms to date, comprising 3,099 samples validated by DNA barcode and phylogenetic tests, representing all 64 orders, 404 families (96%) and 2,333 genera (17%). Using the multi-species coalescent, we inferred a “first pass” angiosperm tree of life from the data, which totalled 824,878 sequences, 489,086,049 base pairs, and 532,260 alignment columns. The tree is strongly supported and highly congruent with existing taxonomy, while challenging numerous hypothesized relationships among orders and placing many genera for the first time. The validated dataset, species tree and all intermediates are openly accessible via the Kew Tree of Life Explorer. This major milestone towards a complete tree of life for all flowering plant species opens doors to a highly integrated future for angiosperm phylogenomics through the systematic sequencing of standardised nuclear markers. Our approach has the potential to serve as a much-needed bridge between the growing movement to sequence the genomes of all life on Earth and the vast phylogenomic potential of the world’s natural history collections.


2016 ◽  
Vol 23 (2) ◽  
pp. 89-102
Author(s):  
Kuldeep Negi ◽  
Vandana Tiwari ◽  
Puran Mehta ◽  
Rajni Rawat ◽  
Saraswati Ojha ◽  
...  

Uttarakhand is a store house of plant genetic resources of several crop groups including ornamentals and seasonal flowering plant species. A wide range of seasonal flowering plants are being grown in the region because of its various and favourable agro-geo climatic zones. Ornamental plant enhances aesthetic value of our environment. There are 8 developmental blocks and 1082 villages in district Nainital of Uttarakhand. Nainital district, is a part of Kumaun region of Uttarakhand. It lies between 29?0.1' to 29?36' 21'' N latitude and 78?50' 53'' to 80?06' E longitude. More than 7.62 lakh population reside in 4064 km2 of geographical area of district Nainital. The district falls under sub-tropical to temperate zones. During the course of field survey (2013-2015), we came across wide range of seasonal flowering plants mostly belong to exotic origin being grown in the home gardens of natives of the region situated in different agro-ecological niches. The present study highlighted a total of 150 seasonal flowering plants with 120 genera belonging to 50 families. These were arranged alphabetically with botanical names followed by vernacular and trade name, family, origin or native place, nature, season with appropriate remarks of variation in shape, size and colour, method of propagation with economic status.


2000 ◽  
Vol 6 ◽  
pp. 209-232 ◽  
Author(s):  
Scott L. Wing

Flowering plants are a classic example of a group arising late in Earth history and yet achieving very high diversity, abundance, and ecological and morphological variety in a great array of environments and climatic conditions on all continents. Thus, the success of flowering plants raises basic questions about how new lineages become inserted into existing terrestrial ecosystems. To what degree did flowering plants replace older lineages competitively, and to what extent did their expansion depend on large-scale environmental disruption or extinction of older groups? Is the higher taxonomic diversity of flowering plants a consequence of higher rates of speciation, lower rates of extinction, or both? Have flowering plants expanded the total area and range of habitats occupied by terrestrial vegetation? What were the effects of the diversification and spread of flowering plants on the structure of habitats and the types of resources available to terrestrial heterotrophs?


1963 ◽  
Vol 43 (3) ◽  
pp. 386-389 ◽  
Author(s):  
Dale Smith

Flowering response of first-year individual plants of nine varieties of red clover was studied at Arlington, Wisconsin. Plant populations of varieties with high winterhardiness had high percentages of non-flowering plants. Winterkilling of plant types increased progressively from non-flowering Type 1 to profuse flowering Type 5.Highly significant correlations were obtained between per cent winterkilling during the first winter with per cent non-flowering plant Type 1 (r = −0.90 and −0.95 during 2 years), per cent of flowering plant Type 5 (r = +0.92 and +0.80), and the total per cent of non-flowering plants (r = −0.90 and −0.94). Flowering response can be used with a high degree of reliability in establishing the probable persistence of new strains relative to standard varieties and as a selection criterion for hardy plants.


Koedoe ◽  
1977 ◽  
Vol 20 (1) ◽  
Author(s):  
B.L. Penzhorn

Additions to the check list of flowering plants of the Mountain Zebra National Park. Thirteen additional flowering plant species are reported from the Mountain Zebra National Park, increasing the total reported to 371 species.


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