Accelerated direct solution of the MoM linear system using block compression and nested factorization

Author(s):  
A. Heldring ◽  
J.M. Rius
2013 ◽  
Vol 101 (2) ◽  
pp. 364-371 ◽  
Author(s):  
A. Heldring ◽  
J. M. Tamayo ◽  
E. Ubeda ◽  
J. M. Rius

2007 ◽  
Vol 55 (11) ◽  
pp. 3220-3228 ◽  
Author(s):  
Alex Heldring ◽  
Juan. M. Rius ◽  
JosÉ Maria Tamayo ◽  
Josep Parron ◽  
Eduard Ubeda

2010 ◽  
Vol 58 (3) ◽  
pp. 1015-1016 ◽  
Author(s):  
A. Heldring ◽  
J. M. Rius ◽  
J. M. Tamayo

2011 ◽  
Vol 59 (2) ◽  
pp. 526-536 ◽  
Author(s):  
Alex Heldring ◽  
Juan M. Rius ◽  
José M. Tamayo ◽  
Josep Parrón ◽  
Eduard Ubeda

Author(s):  
John Kuo ◽  
John S. Pate

Our understanding of nutrient transfer between host and flowering parasitic plants is usually based mainly on physiological concepts, with little information on haustorial structure related to function. The aim of this paper is to study the haustorial interface and possible pathways of water and solute transfer between a number of host and parasites.Haustorial tissues were fixed in glutaraldehyde and embedded in glycol methacrylate (LM), or fixed in glutaraldehyde then OsO4 and embedded in Spurr’s resin (TEM).Our study shows that lumen to lumen continuity occurs between tracheary elements of a host and four S.W. Australian species of aerial mistletoes (Fig. 1), and some root hemiparasites (Exocarpos spp. and Anthobolus foveolatus) (Fig. 2). On the other hand, haustorial interfaces of the root hemiparasites Olax phyllanthi and Santalum (2 species) are comprised mainly of parenchyma, as opposed to terminating tracheads or vessels, implying that direct solution transfer between partners via vessels or tracheary elements may be limited (Fig. 3).


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