SUBJECT D3)ATM traffic shaping
SUBJECT D3-1) Question: What do people mean by the term "traffic shaping"?
Answer: Here is an explicit definition of traffic shaping followed by brief tutorial. Note that a variety of techniques have been investigated to implement traffic shaping. Reference the literature for keywords such as "leaky bucket", "congestion", "rate control", and "policing".
PARAMETERS
There are lots of traffic parameters that have been proposed for resource management. The more important ones are:
For example, an IP router attached to an ATM network might delay some cells slightly in order to reduce the peak rate and rate variance without affecting throughput. An MPEG codec that was operating in a situation where delay wasn't a problem might operate in a CBR mode.
Answer: The cell flow in a connection can be logically split into various cell flows depending on the CLP value of the cell, whether it is 0 or 1.
The following are the cell flows:
The connection and cell flows may be represented as follows:
Connection
|
V
---------------------------
--------------- |
CLP=0 Cell Flow |
--------------- CLP=0+1 Cell Flow
--------------- |
CLP=1 Cell Flow |
--------------- |
---------------------------
To establish a connection we have to specify Peak Cell Rate(PCR),
Sustained Cell Rate(SCR), Maximum Burst Size(MBS) in forward
and backward directions, for each cell flow. So PCR, SCR, etc
are not single values to a connection! We must specify these
values for the cell flows CLP=0, CLP=1 and CLP=0+1. Usually
CLP=0+1 values will be equal to or more than the sum of PCR, etc values
of CLP=0 and CLP=1 cell flows.Depending on the type of the connection we need to specify some (not all) values specific to some cell flows only. TM 4.0 clearly specifies which combinations are valid (in chapter 4). For eg. Tagging can be opted only in VBR.3 conformance defn. in which we specify values for CLP=0 and CLP=0+1 cell flows only.
Right now CDVT is not signalled even in UNI 4.0. Let us say it picks from a standard table for a PCR or SCR value. The cell conformance test will be done for every cell flow seperately. Consider a hypotheical type with tagging option in which we must specify values of CLP=0 and CLP=0+1 cell flows only and cell conformance has to be done for PCRs of these cell flows. A CLP=0 cell will be tested with GCRA(1/PCR0, CDVT0). If it is non-conforming, the cell is deprioritized by tagging it to CLP=1. Now the cell is tested with GCRA(1/PCR01, CDVT01) to check if it is conforming. Note that at any further check point this cell will be checked only with GCRA(1/PCR01, CDVT01) because it is no more in CLP=0 cell flow. A cell sent by source with CLP=1 is checked only with GCRA(1/PCR01, CDVT01) at any place.
Note: PCR0 and CDVT0 are PCR and CDVT of CLP=0 cell flow and PCR01 and CDVT01 are PCR and CDVT of CLP=0+1 cell flow.
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Last Changed 24 November 2002