Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userA ubiquitous ~62-Myr periodic fluctuation superimposed on general trends in fossil biodiversity. I. Documentation
86
0
0.0
(
0
)
Authors
Adrian L. Melott
Ask ChatGPT about the research
No Arabic abstract
We use Fourier analysis and related techniques to investigate the question of periodicities in fossil biodiversity. These techniques are able to identify cycles superimposed on the long-term trends of the Phanerozoic. We review prior results and analyze data previously reduced and published. Joint time-series analysis of various reductions of the Sepkoski Data, Paleobiology Database, and Fossil Record 2 indicate the same periodicity in biodiversity of marine animals at 62 Myr. We have not found this periodicity in the terrestrial fossil record. We have found that the signal strength decreases with time because of the accumulation of apparently resistant long-lived genera. The existence of a 62-Myr periodicity despite very different treatment of systematic error, particularly sampling-strength biases, in all three major databases strongly argues for its reality in the fossil record.
rate research
Read More
Major discrepancies have been noted for some time between fossil ages and molecular divergence dates for a variety of taxa. Recently, systematic trends within avian clades have been uncovered. The trends show that the disparity is much larger for mitochondrial DNA than for nuclear DNA, also that it is larger for crown fossil dates than stem fossil dates. It has been argued that this pattern is largely inconsistent with incompleteness of the fossil record as the principal driver of the disparity. A case is presented that given the expected mutations from a fluctuating background of astrophysical radiation from such sources as supernovae, the rate of molecular clocks is variable and should increase back to a few Ma, before returning to the long-term average rate. This is a possible explanation for the disparity. One test of this hypothesis is to look for an acceleration of molecular clocks 2 to 2.5 Ma due to one or more moderately nearby supernovae known to have happened at that time. Another is to look for reduced disparity in benthic organisms of the deep ocean. In addition, due to the importance of highly penetrating muon irradiation, the disparity should be magnified for megafauna.
Medvedev and Melott (2007) have suggested that periodicity in fossil biodiversity may be induced by cosmic rays which vary as the Solar System oscillates normal to the galactic disk. We re-examine the evidence for a 62 million year (Myr) periodicity in biodiversity throughout the Phanerozoic history of animal life reported by Rohde & Mueller (2005), as well as related questions of periodicity in origination and extinction. We find that the signal is robust against variations in methods of analysis, and is based on fluctuations in the Paleozoic and a substantial part of the Mesozoic. Examination of origination and extinction is somewhat ambiguous, with results depending upon procedure. Origination and extinction intensity as defined by RM may be affected by an artifact at 27 Myr in the duration of stratigraphic intervals. Nevertheless, when a procedure free of this artifact is implemented, the 27 Myr periodicity appears in origination, suggesting that the artifact may ultimately be based on a signal in the data. A 62 Myr feature appears in extinction, when this same procedure is used. We conclude that evidence for a periodicity at 62 Myr is robust, and evidence for periodicity at approximately 27 Myr is also present, albeit more ambiguous.
Time series analysis of fossil biodiversity of marine invertebrates in the Paleobiology Database (PBDB) shows a significant periodicity at approximately 63 My, in agreement with previous analyses based on the Sepkoski database. I discuss how this result did not appear in a previous analysis of the PBDB. The existence of the 63 My periodicity, despite very different treatment of systematic error in both PBDB and Sepkoski databases strongly argues for consideration of its reality in the fossil record. Cross-spectral analysis of the two datasets finds that a 62 My periodicity coincides in phase by 1.6 My, equivalent to better than the errors in either measurement. Consequently, the two data sets not only contain the same strong periodicity, but its peaks and valleys closely correspond in time. Two other spectral peaks appear in the PBDB analysis, but appear to be artifacts associated with detrending and with the increased interval length. Sampling-standardization procedures implemented by the PBDB collaboration suggest that the signal is not an artifact of sampling bias. Further work should focus on finding the cause of the 62 My periodicity.
Determining the mechanisms that drive the evolution of protoplanetary disks is a necessary step to understand how planets form. Here we measured the mass accretion rate for young stellar objects at age >5 Myr, a critical test for the current models of disk evolution. We present the analysis of the spectra of 36 targets in the ~5-10 Myr old Upper Scorpius region for which disk masses were measured with ALMA. We find that the mass accretion rates in this sample of old but still survived disks are similarly high as those of the younger (<3 Myr old) star-forming regions of Lupus and Cha I, when considering the dependence on stellar and disk mass. In particular, several disks show high mass accretion rates >10^-9 Msun/yr while having low disk masses. Furthermore, the median values of the measured mass accretion rates in the disk mass ranges where our sample is complete at a level ~60-80% are compatible in these three regions. At the same time, the spread of mass accretion rates at any given disk mass is still >0.9 dex even at age>5 Myr. These results are in contrast with simple models of viscous evolution, which would predict that the values of the mass accretion rate diminish with time, and a tighter correlation with disk mass at age>5 Myr. Similarly, simple models of internal photoevaporation cannot reproduce the observed mass accretion rates, while external photoevaporation might explain the low disk masses and high accretion rates. A partial possible solution to the discrepancy with the viscous models is that the gas-to-dust ratio of the disks at >5 Myr is significantly different and higher than the canonical 100, as suggested by some dust and gas disk evolution models. The results shown here require the presence of several inter-playing processes, such as detailed dust evolution, external photoevaporation and possibly MHD winds, to explain the secular evolution of protoplanetary disks.
Based on statistical analysis of the complete genome sequences, a remote relationship has been observed between the evolution of the genetic code and the three domain tree of life. The existence of such a remote relationship need to be explained. The unity of the living system throughout the history of life relies on the common features of life: the homochirality, the genetic code and the universal genome format. The universal genome format has been observed in the genomic codon distributions as a common feature of life at the sequence level. A main aim of this article is to reconstruct and to explain the Phanerozoic biodiversity curve. It has been observed that the exponential growth rate of the Phanerozoic biodiversity curve is about equal to the exponential growth rate of genome size evolution. Hence it is strongly indicated that the expansion of genomes causes the exponential trend of the Phanerozoic biodiversity curve, where the conservative property during the evolution of life is guaranteed by the universal genome format at the sequence level. In addition, a consensus curve based on the climatic and eustatic data is obtained to explain the fluctuations of the Phanerozoic biodiversity curve. Thus, the reconstructed biodiversity curve based on genomic, climatic and eustatic data agrees with Sepkoskis curve based on fossil data. The five mass extinctions can be discerned in this reconstructed biodiversity curve, which indicates a tectonic cause of the mass extinctions. And the declining origination rate and extinction rate throughout the Phanerozoic eon might be due to the growth trend in genome size evolution.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
