PHYLOGENY & EVOLUTION
A phylogenetic tree or evolutionary tree is a branching 
diagram or "tree" showing the inferred evolutionary 
relationships among various biological species or other 
entities—their phylogeny—based upon similarities and 
differences in their physical or genetic characteristics. 
The taxa joined together in the tree are implied to have 
descended from a common ancestor. 
In a rooted phylogenetic tree, each node with 
descendants represents the inferred most recent 
common ancestor of the descendants, and the edge 
lengths in some trees may be interpreted as time 
estimates. Each node is called a taxonomic unit.
The idea of a "tree of life" arose from ancient notions of a ladder-like 
progression from lower to higher forms of life (such as in the Great 
Chain of Being). Early representations of "branching" phylogenetic trees 
include a "paleontological chart" showing the geological relationships 
among plants and animals in the book Elementary Geology, by Edward 
Hitchcock (first edition: 1840). 
Charles Darwin (1859) also produced one of the first illustrations and 
crucially popularized the notion of an evolutionary "tree" in his seminal 
book The Origin of Species. Over a century later, evolutionary 
biologists still use tree diagrams to depict evolution because such 
diagrams effectively convey the concept that speciation occurs through 
the adaptive and semirandom splitting of lineages. Over time, species 
classification has become less static and more dynamic.
Rooted tree 
A phylogenetic tree, showing how Eukaryota 
and Archaea are more closely related to each 
other than to Bacteria, based on Cavalier- 
Smith's theory of bacterial evolution. (Cf. 
LUCA, Neomura.) 
A rooted phylogenetic tree is a directed tree 
with a unique node corresponding to the 
(usually imputed) most recent common 
ancestor of all the entities at the leaves of the 
tree. The most common method for rooting 
trees is the use of an uncontroversial 
outgroup—close enough to allow inference 
from sequence or trait data, but far enough to 
be a clear outgroup.
A large gene pool indicates extensive genetic 
diversity, which is associated with robust 
populations that can survive bouts of intense 
selection. Meanwhile, low genetic diversity 
(see inbreeding and population bottlenecks) 
can caus Unrooted trees illustrate the 
relatedness of the leaf nodes without making 
assumptions about ancestry. They do not 
require the ancestral root to be known or 
inferred.[2] Unrooted trees can always be 
generated from rooted ones by simply 
omitting the root. By contrast, inferring the 
root of an unrooted tree requires some 
means of identifying ancestry.
Special tree types[edit] 
This section does not cite any references or sources. Please help improve 
this section by adding citations to reliable sources. Unsourced material may 
be challenged and removed. (October 2012) 
Fig. 3: A spindle diagram, showing the evolution of the vertebrates at class 
level, width of spindles indicating number of families. Spindle diagrams are 
often used in evolutionary taxonomy. 
Fig. 4: A highly resolved, automatically generated tree of life, based on 
completely sequenced genomes.[5][6] 
A dendrogram is a broad term for the diagrammatic representation of a 
phylogenetic tree. 
A cladogram is a phylogenetic tree formed using cladistic methods. This 
type of tree only represents a branching pattern; i.e., its branch spans do 
not represent time or relative amount of character change. 
A phylogram is a phylogenetic tree that has branch spans proportional to 
the amount of character change. 
A chronogram is a phylogenetic tree that explicitly represents evolutionary 
time through its branch spans.
3. Tertiary gene pool (GP-3): Members of this 
gene pool are more distantly related to the 
members of the primary gene pool. The 
primary and tertiary gene pools can be 
intermated, but gene transfer between them is 
impossible without the use of "rather extreme 
or radical measures" [1] such as: 
◦ embryo rescue (or embryo culture, a form of plant 
organ culture) 
◦ induced polyploidy (chromosome doubling) 
◦ bridging crosses (e.g., with members of the 
secondary gene pool).
Main article: Computational phylogenetics 
Phylogenetic trees among a nontrivial number of input sequences are constructed 
using computational phylogenetics methods. Distance-matrix methods such as 
neighbor-joining or UPGMA, which calculate genetic distance from multiple 
sequence alignments, are simplest to implement, but do not invoke an 
evolutionary model. Many sequence alignment methods such as ClustalW also 
create trees by using the simpler algorithms (i.e. those based on distance) of tree 
construction. Maximum parsimony is another simple method of estimating 
phylogenetic trees, but implies an implicit model of evolution (i.e. parsimony). 
More advanced methods use the optimality criterion of maximum likelihood, often 
within a Bayesian Framework, and apply an explicit model of evolution to 
phylogenetic tree estimation.[4] Identifying the optimal tree using many of these 
techniques is NP-hard,[4] so heuristic search and optimization methods are used in 
combination with tree-scoring functions to identify a reasonably good tree that 
fits the data. 
Tree-building methods can be assessed on the basis of several criteria:[7] 
efficiency (how long does it take to compute the answer, how much memory does 
it need?) 
power (does it make good use of the data, or is information being wasted?)
Although phylogenetic trees produced on the basis of 
sequenced genes or genomic data in different species can 
provide evolutionary insight, they have important limitations. 
They do not necessarily accurately represent the evolutionary 
history of the included taxa. The data on which they are 
based is noisy; the analysis can be confounded by genetic 
recombination,[9] horizontal gene transfer,[10] hybridisation 
between species that were not nearest neighbors on the tree 
before hybridisation takes place, convergent evolution, and 
conserved sequences.
The "tree of life 
Evolutionary history of life, an overview of the 
major time periods of life on earth 
Life, the top level for Wikipedia articles on 
living species, reflecting a diversity of 
classification systems. 
Three-domain system (cell types) 
Wikispecies, an external Wikimedia 
Foundation project to construct a "tree of life" 
appropriate for use by scientists
NAME: RAZIA MAHRAM 
ROLL NO. 3035 
CLASS: BS(H) BOTANY 3rd SEMESTER(EVNING) 
UNIVESITY OF EDUCATION OKARA
3035 e1 (2)

3035 e1 (2)

  • 1.
  • 2.
    A phylogenetic treeor evolutionary tree is a branching diagram or "tree" showing the inferred evolutionary relationships among various biological species or other entities—their phylogeny—based upon similarities and differences in their physical or genetic characteristics. The taxa joined together in the tree are implied to have descended from a common ancestor. In a rooted phylogenetic tree, each node with descendants represents the inferred most recent common ancestor of the descendants, and the edge lengths in some trees may be interpreted as time estimates. Each node is called a taxonomic unit.
  • 3.
    The idea ofa "tree of life" arose from ancient notions of a ladder-like progression from lower to higher forms of life (such as in the Great Chain of Being). Early representations of "branching" phylogenetic trees include a "paleontological chart" showing the geological relationships among plants and animals in the book Elementary Geology, by Edward Hitchcock (first edition: 1840). Charles Darwin (1859) also produced one of the first illustrations and crucially popularized the notion of an evolutionary "tree" in his seminal book The Origin of Species. Over a century later, evolutionary biologists still use tree diagrams to depict evolution because such diagrams effectively convey the concept that speciation occurs through the adaptive and semirandom splitting of lineages. Over time, species classification has become less static and more dynamic.
  • 4.
    Rooted tree Aphylogenetic tree, showing how Eukaryota and Archaea are more closely related to each other than to Bacteria, based on Cavalier- Smith's theory of bacterial evolution. (Cf. LUCA, Neomura.) A rooted phylogenetic tree is a directed tree with a unique node corresponding to the (usually imputed) most recent common ancestor of all the entities at the leaves of the tree. The most common method for rooting trees is the use of an uncontroversial outgroup—close enough to allow inference from sequence or trait data, but far enough to be a clear outgroup.
  • 5.
    A large genepool indicates extensive genetic diversity, which is associated with robust populations that can survive bouts of intense selection. Meanwhile, low genetic diversity (see inbreeding and population bottlenecks) can caus Unrooted trees illustrate the relatedness of the leaf nodes without making assumptions about ancestry. They do not require the ancestral root to be known or inferred.[2] Unrooted trees can always be generated from rooted ones by simply omitting the root. By contrast, inferring the root of an unrooted tree requires some means of identifying ancestry.
  • 6.
    Special tree types[edit] This section does not cite any references or sources. Please help improve this section by adding citations to reliable sources. Unsourced material may be challenged and removed. (October 2012) Fig. 3: A spindle diagram, showing the evolution of the vertebrates at class level, width of spindles indicating number of families. Spindle diagrams are often used in evolutionary taxonomy. Fig. 4: A highly resolved, automatically generated tree of life, based on completely sequenced genomes.[5][6] A dendrogram is a broad term for the diagrammatic representation of a phylogenetic tree. A cladogram is a phylogenetic tree formed using cladistic methods. This type of tree only represents a branching pattern; i.e., its branch spans do not represent time or relative amount of character change. A phylogram is a phylogenetic tree that has branch spans proportional to the amount of character change. A chronogram is a phylogenetic tree that explicitly represents evolutionary time through its branch spans.
  • 7.
    3. Tertiary genepool (GP-3): Members of this gene pool are more distantly related to the members of the primary gene pool. The primary and tertiary gene pools can be intermated, but gene transfer between them is impossible without the use of "rather extreme or radical measures" [1] such as: ◦ embryo rescue (or embryo culture, a form of plant organ culture) ◦ induced polyploidy (chromosome doubling) ◦ bridging crosses (e.g., with members of the secondary gene pool).
  • 8.
    Main article: Computationalphylogenetics Phylogenetic trees among a nontrivial number of input sequences are constructed using computational phylogenetics methods. Distance-matrix methods such as neighbor-joining or UPGMA, which calculate genetic distance from multiple sequence alignments, are simplest to implement, but do not invoke an evolutionary model. Many sequence alignment methods such as ClustalW also create trees by using the simpler algorithms (i.e. those based on distance) of tree construction. Maximum parsimony is another simple method of estimating phylogenetic trees, but implies an implicit model of evolution (i.e. parsimony). More advanced methods use the optimality criterion of maximum likelihood, often within a Bayesian Framework, and apply an explicit model of evolution to phylogenetic tree estimation.[4] Identifying the optimal tree using many of these techniques is NP-hard,[4] so heuristic search and optimization methods are used in combination with tree-scoring functions to identify a reasonably good tree that fits the data. Tree-building methods can be assessed on the basis of several criteria:[7] efficiency (how long does it take to compute the answer, how much memory does it need?) power (does it make good use of the data, or is information being wasted?)
  • 9.
    Although phylogenetic treesproduced on the basis of sequenced genes or genomic data in different species can provide evolutionary insight, they have important limitations. They do not necessarily accurately represent the evolutionary history of the included taxa. The data on which they are based is noisy; the analysis can be confounded by genetic recombination,[9] horizontal gene transfer,[10] hybridisation between species that were not nearest neighbors on the tree before hybridisation takes place, convergent evolution, and conserved sequences.
  • 10.
    The "tree oflife Evolutionary history of life, an overview of the major time periods of life on earth Life, the top level for Wikipedia articles on living species, reflecting a diversity of classification systems. Three-domain system (cell types) Wikispecies, an external Wikimedia Foundation project to construct a "tree of life" appropriate for use by scientists
  • 11.
    NAME: RAZIA MAHRAM ROLL NO. 3035 CLASS: BS(H) BOTANY 3rd SEMESTER(EVNING) UNIVESITY OF EDUCATION OKARA