A theoretical morphologic analysis of convergently evolved erect helical colony form in the Bryozoa

Paleobiology ◽  
2000 ◽  
Vol 26 (4) ◽  
pp. 556-577 ◽  
Author(s):  
George R. McGhee ◽  
Frank K. McKinney

Exploration of the theoretical morphospace of erect helical colony form in Bryozoa, created by McKinney and Raup (1982), reveals that only a small volume of the three-dimensional space of hypothetical form is occupied by actual colonies of the Paleozoic fenestrates (Class Stenolaemata) Archimedes and Helicopora, helical species of the cheilostome (Class Gymnolaemata) Bugula, and the cyclostome (Class Stenolaemata) Crisidmonea archimediformis. Actual helical-colony bryozoans are not found in regions of the morphospace characterized by colony geometries that possess the largest surface areas of filtration sheet. Examination of computer-simulated colonies in the theoretical morphospace reveals that, although possessing high surface areas, colonies in the empty region of high-surface-area morphospace possess other aspects of geometry that are unrealistic as filter-feeding geometries: the filtration-sheet whorls are held at small acute angles to the central colony axis and are deeply nested within one another, both of which are disadvantageous conditions for the system of filter feeding used by the extant cheilostome Bugula, and presumably by extinct helical-colony bryozoans as well.Even though actual bryozoans are found only in the low to intermediate surface-area regions of the theoretical morphospace, surface area of filtration sheet is a major determinant of form in these helical colonies, as is evidenced by a negative correlation in values of the parameters BWANG and ELEV exhibited by the colony data. Minimum values of BWANG are even further constrained by the apparent need of the Archimedes colonies to maintain filtration-sheet branching densities within the range of 20 to 50.

Author(s):  
Ketki Lichade ◽  
Yizhou Jiang ◽  
Yayue Pan

Abstract Recently, many studies have investigated additive manufacturing of hierarchical surfaces with high surface area/volume (SA/V) ratios, and their performance has been characterized for applications in next-generation functional devices. Despite recent advances, it remains challenging to design and manufacture high SA/V ratio structures with desired functionalities. In this study, we established the complex correlations among the SA/V ratio, surface structure geometry, functionality, and manufacturability in the Two-Photon Polymerization (TPP) process. Inspired by numerous natural structures, we proposed a 3-level hierarchical structure design along with the mathematical modeling of the SA/V ratio. Geometric and manufacturing constraints were modeled to create well-defined three-dimensional hierarchically structured surfaces with a high accuracy. A process flowchart was developed to design the proposed surface structures to achieve the target functionality, SA/V ratio, and geometric accuracy. Surfaces with varied SA/V ratios and hierarchy levels were designed and printed. The wettability and antireflection properties of the fabricated surfaces were characterized. It was observed that the wetting and antireflection properties of the 3-level design could be easily tailored by adjusting the design parameter settings and hierarchy levels. Furthermore, the proposed surface structure could change a naturally-hydrophilic surface to near-superhydrophobic. Geometrical light trapping effects were enabled and the antireflection property could be significantly enhanced (>80% less reflection) by the proposed hierarchical surface structures. Experimental results implied the great potential of the proposed surface structures for various applications such as microfluidics, optics, energy, and interfaces.


2007 ◽  
Vol 19 (17) ◽  
pp. 4367-4372 ◽  
Author(s):  
Ajayan Vinu ◽  
Pavuluri Srinivasu ◽  
Dhanashri P. Sawant ◽  
Toshiyuki Mori ◽  
Katsuhiko Ariga ◽  
...  

2014 ◽  
Vol 617 ◽  
pp. 187-190 ◽  
Author(s):  
Te Wei Chiu ◽  
Yi Wei Feng

In this study, the effects of glycine-nitrate ratios and postcombustion chemical treatment on the phase evolution and surface area of CuCrO2powders were investigated. The pure phase of CuCrO2powders was obtained at a glycine-nitrate ratio of 1.2–1.4. When the glycine-nitrate ratio was higher than 1.9, the Cu ions were reduced to Cu(0) and the phase of Cu metal and Cr2O3were observed. However, when the glycine-nitrate ratio was lower than 1.1, the Cu ions were partially maintained as Cu(2+), and a bluish residue was observed. As-combusted CuCrO2powder with a high surface area (50 m2/g) was obtained at a glycine-nitrate ratio of 1.2. Furthermore, a high surface area (> 60 m2/g) was obtained by leaching as-combusted CuCrO2powder with diluted nitric acid.


1986 ◽  
Vol 73 ◽  
Author(s):  
Joseph R. Fox ◽  
Douglas A. White ◽  
Susan M. Oleff ◽  
Robert D. Boyer ◽  
Phyllis A. Budinger

AbstractSol-gel precursors to silicon carbide have been prepared using trifunctional chloro and alkoxysilanes which contain both the silicon and carbon necessary for SiC formation. Crosslinked gels having the ideal formula [RSiO1 5].]n have been synthesized by a hydrolysis/condensation scheme for a series of saturated and unsaturated R groups. The starting gels have been characterized by a variety of elemental analysis, spectroscopic and physical measurements including IR. XRD. TGA.. surface area and pore volume. A particularly powerful method for characterizing these gels is the combination of 13C and 29 Si solid state NMR which can provide information about the degree of crosslinking as well as residual hydroxy/alkoxy content.The controlled pyrolysis of these gels has been used to prepare silicon carbide-containing ceramic products with surface areas in excess of 600m2/gm. The pyrolysis products are best described as a partially crystalline, partially amorphous mixture of β-SiC, silica and carbon. The effect of carbon chain length and the degree of unsaturation in the R group on the composition and surface area of the product has been determined. The origin of the high surface area of the pyrolysis products has been identified and its implications on potential uses of these materials is discussed.


1994 ◽  
Vol 368 ◽  
Author(s):  
Timothy P. Palucka ◽  
Nicholas G. Eror ◽  
Thomas A. Mcnamara

ABSTRACTAn oxidative catalytic route for the decomposition of nerve gases was investigated using hydroxyapatite (HA, chemical composition Ca10(PO4)6(OH)2) and its partially fluorinated analog fluorhydroxyapatite (FHA, Ca10(PO4)6Fx(OH)2−x). Samples were prepared with surface areas ranging from 34 to 238 m2/g to study surface area effects; 1.2 wt. % platinum was deposited on one substrate to investigate the effect of a transition metal on activity and selectivity. Reaction studies were performed using dimethyl methylphosphonate (DMMP), a nerve gas simulant, in a stream of 80 percent nitrogen and 20 percent oxygen at 573 K and atmospheric pressure. High surface area FHA samples showed an increase in the "protection period" (period of 100% conversion) with increasing fluorine substitution; such an increase was not seen for low surface area FHA samples. In the absence of platinum, the reaction products were methanol and dimethyl ether; with platinum, CO2 was also obtained.


1994 ◽  
Vol 371 ◽  
Author(s):  
Chunling Liu ◽  
Sridhar Komarneni

AbstractHigh surface area ethyltrimethoxysilane (ETMS) modified silica aerogels and xerogels were synthesized by cohydrolyzing the mixtures of ETMS and tetramethylorthosilicate (TMOS). The effects of ETMS content, pH value and solvent addition were investigated. The surface area, pore structure and hydrophobicity were studied using nitrogen and water sorption measurements. By ETMS modification of TMOS gels, high surface area, density and hydrophobicity were achieved. The 25 mole% ETMS-75 mole% TMOS was found to be the best composition for both aerogel and xerogel, which are hydrophobic and have surface areas of 1221 and 832 m2/g, respectively.


2018 ◽  
Vol 3 (3) ◽  
pp. 244-250 ◽  
Author(s):  
Dereck N. F. Muche ◽  
Flavio L. Souza ◽  
Ricardo H. R. Castro

A non-system specific method for the synthesis of metal oxide nanoparticles with high homogeneity, spherical morphology and high surface areas is proposed based on an aqueous precipitation.


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