Phylogenetic Relationships Flashcards

1
Q

Phylogenetic relationships of organisms are very important to understand the *** of different groups.

A

evolutionary trends

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2
Q

According to *** all existing groups of organisms have evolved from the progenitors in the past. The ancestral groups might be evolved along certain definite pathways to have given rise to the present-day forms, which fall into distinct groups according to their similarity.

A

Darwin’s theory

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3
Q

The pathways of evolutionary changes among
organisms can be understood by studying the **, **, **, **, and ***.

A
  • concepts of primitive and advanced characters
  • mono and holophytic
  • para and polyphyletic
  • homology and analogy
  • parallel and convergent evolution
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4
Q

Determining the primitive and advanced character-states or estimating the *** are the first step in constructing phylogeny.

A

polarity of characters

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5
Q

The existence of some general evolutionary trends in the angiosperms is now generally admitted for determining ** and **.

A

primitive and advanced characters

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6
Q

** (1915) enumerated many evolutionary trends which have been followed by ** in their modern classifications.

A
  • Bessey
  • Takhtajan, Cronquist, Hutchinson, and Thorne
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7
Q

The terms ‘primitive character’ and ‘advanced character’ are first time used by ***

A

Sporne (1948)

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8
Q

means ‘one which possessed by a present-day taxon and was also possessed by its ancestors’.

A

primitive character

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9
Q

‘one which possessed by a present-day taxon and not possessed by its ancestors, that is, it replaced an ancestral character during evolution’.

A

advanced character

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10
Q

Based on primitive and advanced characteristics several systematists proposed and established different principles in plant taxonomy. who are those?

A

Swingle
Bessey
Sporme
Hutchinson
Heywood
Takhtajan
Thorne

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11
Q

Swingle has proposed *** which have been
uniformly accepted by the plant taxonomists.

A

36 principles in evolutionary taxonomy

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12
Q

Bessey’s system was based on a series of ** or **. He used the principles in determining the ** or ** of plant groups.

A
  • “dicta”
  • statements of guiding principles
  • degree of primitiveness
  • evolutionary advancement
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13
Q

*** are based on different trends in plant morphology. Among these, Swingle’s and Bessey’s General principles are explained in detail for a better understanding of primitive and advanced characteristics of angiosperms.

A

Hutchinson’s principles

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14
Q

” Plant relationships are up and down genetic lines and these must constitute the
framework of phylogenetic taxonomy. This will naturally form a branching but not
reticulate structure.”

A

Swingle’s Principles

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15
Q

“Evolution does not necessarily involve all organs of the plant at one time or in the
same direction. One organ may be advancing while another is stationary or
retrogressing.”

A

Swingle’s Principles

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16
Q

**, also known as the **,” suggests that the genus Citrus should be treated as a monotypic genus, meaning that all cultivated citrus varieties (lemons, oranges, grapefruits, etc.) should be considered as members of a single species, Citrus sinensis.

A
  • Swingle’s principle
  • monotypic principle
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17
Q

the cultivated citrus plants are believed to have originated from a few ancestral species that underwent hybridization and selection over time. He argued that the cultivated citrus varieties represent different cultivars and variations within a single species, rather than distinct species. Who is this?

A

Walter T. Swingle

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18
Q

He emphasized the importance of considering evolutionary relationships and shared ancestry when classifying plants. He argued that classification should be based on the natural relationships among organisms rather than solely on superficial morphological features.

A

Charles E. Bessey

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19
Q

developed the concept of the “phylogenetic tree” or “evolutionary tree” to represent the relationships among different species. This tree-like diagram visually depicts the evolutionary history and branching patterns of organisms, showing their common ancestors and the divergence of lineages over time.

A

Charles E. Bessey

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20
Q

Primitive or Advanced character: Perennials

A

Primitive

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21
Q

Primitive or Advanced character: Erect Plants

A

Primitive

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22
Q

Primitive or Advanced character: Monocotyledons

A

Advanced

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23
Q

Primitive or Advanced character: Oligostemonous - with fewer stamens

A

Advanced

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24
Q

Primitive or advanced? Homogenous structures (with many
similar parts)

A

Primitive

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25
Q

Primitive or advanced? Heterogenous structures (with fewer and
dissimilar parts)

A

Advanced

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26
Q

Primitive or advanced? Simple unbranched stem

A

Primitive

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27
Q

Primitive or advanced? Heterophytic (non-chlorophyllous plants)

A

Advanced

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28
Q

Primitive or advanced? Powdery pollen

A

Advanced

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29
Q

Primitive or advanced? Polycarpy- with numerous carpels

A

Primitive

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30
Q

Primitive or advanced?Bisexualflowers (Monoclinous)

A

Primitive

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31
Q

Primitive or advanced? Non-endospermic seeds

A

Advanced

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32
Q

Primitive or advanced? Endospermic seeds

A

Primitive

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33
Q

Primitive or advanced?
1. Annuals
2. Terrestrial plants with normal habit
3. Dicotyledons
4. Branching stem
5. Parallel venation of leaves

A
  1. advanced
  2. primitive
  3. primitive
  4. advance
  5. advanced
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34
Q

Primitive or advanced?
1. Flowers with petals
2. Flowers apetalous (aphansis)
3. Polystemonous -with numerous
stamens
4. Multiple fruits
5. Simple and aggregate fruits

A
  1. primitive
  2. advanced
  3. primitive
  4. advanced
  5. primitive
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35
Q

Primitive or advanced?
1. Unisexual flowers (Diclinous)
2. Polypetalous
3. Gamopetalous
4. Simple leaves
5. Compound leaves

A
  1. advanced
  2. primitive
  3. advanced
  4. primitive
  5. advanced
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36
Q

Primitive or advanced?
1. Tap root system
2. Adventitious root system
3. Aquatic plants, epiphytes, parastites and
saprophytes

A
  1. primitive
  2. advanced
  3. advanced
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37
Q

Primitive or advanced?
1. Tap root system
2. Adventitious root system
3. Aquatic plants, epiphytes, parastites and
saprophytes
4. Woody trees
5. Shrubs and herbs

A
  1. primitive
  2. advanced
  3. advanced
  4. primitive
  5. advanced
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38
Q

Primitive or advanced?
1. Climbing plants
2. Holophytic(chlorophyllous plant
3. Oligomerous flowers with lesser number
of parts with whorled arrangement
4. Polymerous flowers with numerous
floral parts with spiral arrangement
5. Seeds with two coats
6. Apocarpy
7. Syncarpy
8. Seeds with one coat

A
  1. advanced
  2. primitive
  3. advanced
  4. primitive
  5. primitive
  6. primitive
  7. advanced
  8. advanced
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39
Q

Primitive or advanced?
1. Curved embryo
2. Straight embryo
3. Alternate or spiral phyllotaxy
4. Opposite or whorled
5. Perigyny and Epigyny
6. Hypogyny

A
  1. advanced
  2. primitive
  3. primitive
  4. advanced
  5. advanced
  6. primitive
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40
Q

Primitive or advanced?
1. Epigeal germination
2. Hypogeal germination
3. Oligocarpy- with fewer carpels
4. Apostemonous -Free stamens
5. Synstemonous - Stamens with adhesion or
cohesion

A
  1. primitive
  2. advanced
  3. advanced
  4. primitive
  5. advanced
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41
Q

Primitive or advanced
1. Dioecious
2. Monoecious
3. Zygomorphic flowers
4. Actinomorphic flowers
5. Reticulate venation of leaves

A
  1. advanced
  2. primitive
  3. advanced
  4. primitive
  5. primitive
42
Q

Primitive or advanced
1. Inflorescence
2. Solitary flower
3. Leaves persistent (evergreen)
4. Leaves deciduous
5. Scalariform vessels
6. Pitted vessels

A
  1. advanced
  2. primitive
  3. primitive
  4. advanced
  5. primitive
  6. advanced
43
Q

Advanced or primitive?
1. Few, collateral bundles arranged in a
ring
2. Numerous bundles, scattered
3. Tracheae or vessels
4. Tracheids

A
  1. primitive
  2. advanced
  3. advanced
  4. primitive
44
Q

The earlier first appearance of a character-state was ** and the more recent strata of a character-state is ** .

A
  • primitive
  • advanced
45
Q

** and ** are the two major contributing factors of evolutionary divergence for determining primitive and advanced character states. *** have been traditionally believed to be random.

A
  • Mutation
  • recombination
  • Mutations
46
Q

According to * and present updated knowledge, mutations are not wholly random. They can be called as ‘’ instead of ‘**’ (Cronquist, 1969).

A
  • Neo-Darwinian concepts
  • differential mutations
  • random mutations
47
Q

** are the suppliers of raw materials for evolutionary changes and ** set the directional trends in evolution.

A
  • Mutations
  • differential mutations
48
Q

Developmental processes and consequent character-states involve complex and
precise gene interactions are likely to be *** than those that involve simple interactions.

A

more advanced

49
Q

If the *** is more complicated, the structure will be more specialized.

A

ontogeny

50
Q

In 1922, *** proposed one concept about primitiveness. According to him the character-state possessed by the largest number of member taxa of a given group likely to be more primitive in the group.

A

Willis

51
Q

**, **, and ***also supported Willis’ view. For example, in a group of 100 species of which 95 have the character-state ‘X’ and the rest have the alternative state ‘Y’, it is almost certain that the ancestor also had ‘X’ (Valenentine, 1978). This concept gives different results depending upon whether we consider only living representatives or also take the extinct groups into account.

A

Wagner, Tayler & Campbell

52
Q

* modified the concept of Willis, and redefined the ‘primitive characters’
as the ones that are ‘
*’, because they would display the ancestral characters better than would the modern forms. He stated the example of Poaceae, where most of the members have a bifid style and two lodicules, but the primitive states of this family are a trifid style and three lodicules, which is rather uncommon in it.

A
  • Stebbins (1974)
  • most common in the members of the group that first achieved widespread success
53
Q

** suggested that primitive characters have a tendency to occur together, within a given group, because they are correlated. In contrast, ** viewed that characters are correlated not because they are primitive, but because they are functionally related.

A
  • Sporne (1948, 1977)
  • Crowson (1970)
54
Q

The evolutionary rates in primitive and advanced characters or taxonomic groups are ** in different lineages. The rate of evolution is influenced not only by the inherent characteris ** .

A
  • different
  • environmental factors
55
Q

Some groups are capable of fast evolution (), some evolve at moderate speed (), and some are still undergoing slow evolution (***).

A
  • tachytelic
  • horotelic
  • bradytelic
56
Q

Populations of the same species and even different organs of the same taxon are known to have evolved at **. Hence, ** suggested that the organs of flowering plants tend to evolve on four more or less independent lines, namely (1-4)

A
  • different speeds
  • Davis and Heywood (1963)
    1. underground parts
    2. aerial shoots
    3. flowers
    4. fruits.
57
Q

A *** is usually ancestral where as a primitive taxon may not (Heywood, 1977).

A

primitive character

58
Q

The only possible way of defining and recognizing primitive taxa is in terms of their possession of a ** ; in contrast, ** are revealed by the relatively few primitive characters that they retain (Sporne, 1977).

A
  • relatively large number of primitive characters
  • advanced taxa
59
Q

A primitive or advanced group may be ancient or recent depending upon the time when they ** from their respective ancestral group. Each splitting in the phyletic line implies an ** .

A
  • split
  • advancement
60
Q

Taxa whose members have descended from a common ancestor are called ‘*** ’. In another way, this means a single phylum has derived or is supposed to have derived from one parental form.

A

monophyletic

61
Q

All members or species of a *** taxon
descend either from the same parents or the same population or same species.

A

monophyletic

62
Q

A class is *** if all its lineages ancestral to that class originated from the same family.

A

monophyletic

63
Q

The phenomenon of the origin of monophyletic taxa is called *** .

A

monophyletic evolution or monophyly

64
Q

In 1961, *** defined monophyly as ‘the derivation of a taxon through one or more lineages from one immediately ancestral taxon of the same or lower rank’.

A

Simpson

65
Q

** has defined a monophyletic group as one that contains all the descendants of a group of individuals who at their time belonged to a single biological species. Here the emphasis is not only on common ancestry but also on including all descendants of a group in the same taxon. ** is a cladistic concept and should therefore be defined in terms of a cladistic relationship.

A
  • Henning
  • Monophyly
66
Q

*** defined a monophyletic as one whose most recent group common ancestor is cladistically a member of that group.

A

Ashlock (1971)

67
Q

** discussed the definition of monophyly at length and rejected the requirement of cladistic membership for the ancestral group as impractical. Before one can trace all the members of a taxon back to a common ancestor, one is outside the limits of the group. There was never an ** that was ancestor to all the other **. For any ** the common ancestor may not be an ** but **

A
  • Cronquist (1973)
  • original Angiosperm
  • Angiosperms
  • angiosperm
  • angiosperm
  • some kind of gymnosperm.
68
Q

Cronquist’s idea seems relevant to * of a monophyletic group as one derived from an ancestral form that would be regarded as belonging to the taxon in question. It is called as ‘*’.

A
  • Heslop-Harrison’s (1958) definition
  • genealogical monophyly
69
Q

Monophyly and Polyphyly have been redefined by ** and ** in phenetic terms. A monophyletic group is considered to be one that does not contain organisms that are more closely related to organisms in another group of the same rank. The ** can be determined by the association of their characters. If a given character occurs in all groups under consideration in the same or similar combinations of characters that are not functionally interrelated, the character state is most likely to be ** in that particular group.

A
  • Maze & Hughes (1973)
  • phylogeny of monophyletic groups
  • monophyletic
70
Q

Taxa whose members have descended from two or more ancestral lineages through convergent or parallel evolution is called ** . The phenomenon of origin of polyphyletic taxa is called ** or ***

A
  • polyphyletic
  • polyphyletic evolution or polyphyly
71
Q

A ** is defined as one in which the most recent common ancestor is not cladistically a member of that group. It contains taxa from more than one clade and excludes the common ancestor (Funk, 1985). Although admittedly unnatural, it may be too useful to be replaced by a more natural classification. Some taxonomists considered the ancestry of Angiosperms as **

A
  • polyphyletic group
  • polyphyletic
72
Q

Taxonomists usually retain the polyphyletic groups which show ** , while those displaying ** are broken into monophyletic units

A
  • continuous variation
  • discontinuities
73
Q

The concepts of monophyly and polyphyly are purely relative and meaningful only with reference to a particular group of organisms. In cladistics, a monophyletic and polyphyletic approach is necessary in order to permit the natural and useful grouping of organisms. There is a continuous gradation from ** to ** (Cronquist, 1969)

A
  • strict monophylesis
  • extreme polyphylesis
74
Q

In 1971 Ashlock defined a monophyletic group as one whose most recent common ancestor is cladistically a member of that group. When such a group contained all the descendants of the most recent common ancestor, it is called ** , and when it did not contain all such descendants then it is termed ** .

A
  • holophyletic
  • paraphyletic
75
Q

Paraphyletic taxa are defined by ** (characters that are not unique or novel at a given level of cladogram). All members of a paraphyletic group have a common ancestor, but the group is not monophyletic because it does not contain all possible members of the clade. According to *, it does not require all descendants of the ancestral taxon to be included in a monophyletic taxon, and is often called ‘’ (Stevens, 1986).

A
  • plesiomorphies
  • genealogical monophyly
  • paraphyletic
76
Q

In 1971 ** redefined the phylogenetic terms with reference to a **i.e. sister-group systems. He considers paraphyly to be more similar to polyphyly and so does not use the term holophyly because in his view it is superfluous.

A
  • Nelson
  • theory of relationship
77
Q

Nelson defines monophyletic groups as ‘’, which include all species or groups of species assumed to be descendants of a hypothetical ancestral species and considers those which do not include all the descendants as non-monophyletic. Among the sister groups, there are two types i.e. ‘’ which lacking one species or a monophyletic species group are called **, and ** or monophyletic species groups that together do not form a monophyletic group are called ***.

A
  • complete sister-group systems
  • incomplete sister-group systems
  • paraphyletic
  • those lacking two or more species
  • polyphyletic
78
Q

** a zoologist was probably the first person who explained and defined the terms ‘Homology’ and ‘Analogy’. According to him, ** means ‘the same organ in different animals under every variety of form and function’; *** means a part or an organ in one animal which has the same function as another part or organ in a different animal’

A
  • Robert Owen
  • homology
  • analogy
79
Q

the criteria helped to identify homologous and analogous characters:

A
  1. Similarity in position and origin.
  2. Similarity in anatomical and histological characters.
  3. Similarity in developmental pattern.
80
Q

** can be defined as the relation between parts that results from their development from corresponding embryonic parts. When it is applied to similar organs of the same individual, it is called **. For example, the leaves of X and Y are homologous and the leaves of X or Y are **among themselves. ** are often very dissimilar and have different functions (Dahlgren et al., 1985).

A
  • General homology
  • serial homology
  • serially homologous
  • Homologous structures
81
Q

The common inheritance in different taxonomic groups leads to arise the similarities among them, these similarities are called **. If they arise due to other than inheritance, they are termed as **. Since the ** and ** characters indicate phylogenetic relationships among the different taxonomic groups, recognition of these characters is one of the primary concerns of *** (Jardine, 1967).

A
  • homologous characters
  • homoplastic
  • homologous and homoplastic
  • biosystematics
82
Q

The *** is useful for the identification of related groups and can act as a valuable taxonomic guide. According to his law, similar series of heritable variations occur in related groups because of their common possession of ancestral genes, which are likely to mutate in similar variations.

A
  • Vavilov’s law of homologous variation
83
Q

The concept of ** reflects the degree of structural or historical development or evolutionary relationship between parts rather than a certain absolute correspondence of parts (Meyen, 1973). A good example is ** in plants.

A
  • homology
  • cyanogenesis
84
Q

According to * concept that a ‘’ is a modified shoot, uniaxial and floral appendages are homologous. It has long been accepted and is the basis for almost all subsequent botanical works. Later it has proved that flowers are ** in nature and floral appendages are not homologous.

A
  • Goethean
  • flower
  • pluriaxial
85
Q

According to **, in modern taxonomy, the recognition of homology in practice is perhaps not even in terms of positional, developmental, functional, or anatomical criteria, but more simply on a similarity of structures in two groups that are believed to be related. Hence, in ** , two structures are considered to be homologous if they satisfy two criteria, like similarity and congruence with phylogeny (Levin, 1985).

A
  • Stevens (1984)
  • cladistics
86
Q

In epiphyllous angiosperms, despite morphological and developmental similarities, there are fertile and sterile leaves that cannot be homologous, because the former differs due to the presence of the epiphyllous shoot. These fertile leaves are absolutely homologous neither with shoots nor with leaves. This phenomenon was named by Dickinson (1978) as a ‘***’. This concept recognizes the possibility of structures homologous with more than one kind of organ or organ system.

A
  • semiquantitative homology concept
87
Q

An ** can be defined as the resemblance of structures that depend upon the similarity of
function. If similarities are arising in diverse and unrelated taxonomic groups due to convergent
evolution they are called **
. ***includes analogy, which in turn results in convergent evolution

A
  • analogy
  • analogous characters
  • Homoplasy
88
Q

** redefined homology and analogy concepts. ** is the occurrence of similar features in two or more organisms that can be traced back to the same feature in their common ancestor, and ** is those which cannot be traced back to the same feature in the common ancestor. These concepts are useful to study **.

A
  • Mayr (1969)
  • Homology
  • analogy
  • evolutionary taxonomy
89
Q

In **, the distinction between homologous and analogous characters was one of great importance, whereas in ** its importance has increased more due to its interpretable value in evolutionary terms especially in forming natural groups.

A
  • pre-Darwinian biology
  • post-Darwinian biology
90
Q

The homology and analogy concepts are helped in the works of ** (1980) and ** (1984).

A
  • Parenti’s ‘Phylogenetic analysis of land plants’
  • Rodman et al., ‘Revised classification of Centrospermae’
91
Q

When two or more closely related groups tend to evolve by acquiring similar characteristics, it is termed as **, and when distantly related or unrelated ones acquire similar character-states, it is termed as **.

A
  • parallelism
  • convergence
92
Q

In living organisms, the dissimilarities are . They are the result of ‘’ or ‘***’ which are useful to recognize them. The similarities of living organisms are also common which help us to synthesize them into higher rank or categories.

A
  • widespread
  • divergent
  • radiating evolution
93
Q

similar features can develop separately into two
or more genetically similar, fairly closely related lineages.

A

Parallel evolution (Parallelism) by Heywood

94
Q

the similar features can develop separately in two or
more genetically diverse and not closely related lineages and not due to common ancestry.

A

Convergent evolution (Convergence) by Heywood

95
Q

When an essentially similar evolutionary trend has developed independently in two or more lineages where originally similar organs were involved to give rise to homologous, ecologically, and typologically similar structures

A

Parallel evolution (Parallelism) by Dahlgren

96
Q

When more or less dissimilar organs become similar and/or ecologically equivalent along independent evolutionary lines

A

Convergent evolution (Convergence) by Dahlgren

97
Q

development proceeding from similar forms to new
similar forms.

A

Parallel evolution (Parallelism) by Kuprianova

98
Q

development proceeding from dissimilar forms to
similar ones.

A

Convergent evolution (Convergence) by Kuptianova

99
Q

According to **, although both parallelism and convergence can be explained in terms of environmental action, there is a greater emphasis on the genotype in the former, whereas in the latter the emphasis falls on environmental influence and similar selection pressures. These two have wide implications in evolutionary taxonomy to arrive at taxonomic conclusions (Cronquist, 1969) because evolutionary ** is taken to be an indicator of
relationship and hence is given due weight, along with other features.

A
  • Meyen (1973)
  • parallelism
100
Q

Parallel and convergent evolution has brought about character similarities among diverse plant groups, related and unrelated, and to different degrees. These two are relative and meaningful in ***.

A

evolutionary taxonomy

101
Q

‘***’ is the ability of plants to release hydrocyanic acid when injured, and about 2056 species of diverse groups of vascular plants have this capability (Hegnauer, 1977).

A

cyanogenesis

102
Q

the taxonomic group ‘* ’, which consists of several arborescent families with a similar ‘*’ which were long supposed to be a homogenous group.

A
  • Amentiferae
  • syndrome of anemophilous characteristics