Quantitative characterization of various oil contents and spatial distribution in lacustrine shales: Insight from petroleum compositional characteristics derived from programed pyrolysis

2022 ◽  
pp. 105522
Author(s):  
Ming Guan ◽  
Xiaoping Liu ◽  
Zhijun Jin ◽  
Jin Lai ◽  
Jie Liu ◽  
...  
CORROSION ◽  
10.5006/3551 ◽  
2020 ◽  
Vol 76 (9) ◽  
pp. 861-870 ◽  
Author(s):  
Adeyinka Abass ◽  
Kentaro Wada ◽  
Hisao Matsunaga ◽  
Heikki Remes ◽  
Tiina Vuorio

Nearest neighbor analysis (NNA)-based procedures are proposed for the quantitative characterization of the spatial distribution of corrosion pits in metals. After the exposure of a carbon steel to a 3.5% NaCl solution mist, the results derived from observation of corrosion pit initiation and growth were used to justify the applicability of this approach. The pits initially comprised clusters that were superimposed on a randomly distributed background set. The clustered pits subsequently coalesced, evolving into a more random pit arrangement. Furthermore, it was revealed that in the early stages, the spatial pit distribution can be predicted via inspection of surface inclusions prior to the corrosion process.


2019 ◽  
Author(s):  
Nathan J. Robinson ◽  
Emily Lazo-Wasem ◽  
Brett O. Butler ◽  
Eric A. Lazo-Wasem ◽  
John D. Zardus ◽  
...  

ABSTRACTThere is a wealth of published information on the epibiont communities of sea turtles, yet many of these studies have exclusively sampled epibionts found only on the carapace. Considering that epibionts may be found on almost all body-surfaces and that it is highly plausible to expect different regions of the body to host distinct epibiont taxa, there is a need for quantitative comparative studies to investigate spatial variation in the epibiont communities of turtles. To achieve this, we measured how total epibiont abundance and biomass on olive ridley turtles Lepidochelys olivacea varies among four body-areas of the hosts (n = 30). We show that epibiont loads on olive ridleys are higher, both in terms of number and biomass, on the skin than they are on the carapace or plastron. This contrasts with previous findings for other hard-shelled sea turtles, where epibionts are usually more abundant on the carapace. Moreover, the arguably most ubiquitous epibiont taxon for other hard-shelled sea turtles, the barnacle Chelonibia spp., only occurs in relatively low numbers on olive ridleys, while the barnacles Stomatolepas elegans and Platylepas hexastylos are far more abundant. We postulate that these differences between the epibiont communities of different sea turtle taxa could indicate that the carapaces of olive ridley turtles provide a more challenging substratum for epibionts than do the hard shells of other sea turtles. In addition, we conclude that it is important to conduct full body surveys when attempting to produce a holistic qualitative or quantitative characterization of the epibiont communities of sea turtles.


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