2nd PU Biology 2014 PDF
2nd PU Biology 2014 PDF
2nd PU Biology 2014 PDF
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MID-TERM
. 2AI4
I P.U.C.
BroLocY (36)
Time: 3% Hours
GENERAL INSTRUCTIONS
i
iii.
10X
1:
10
g.
'
9'
co
PART.A
Answer the folowing questions in one word or one sentence
each.
1. Whatisapomixis? 2.Defineimplantation.
3. Whatismenarche? 4. Whatismeantbytubectomy?
5. NamethenitogenbasespresentinDNAr o. wtratistanslation?
PART. B
following.
ib
10.
lo
II.
Question paper has four parts A, B, c and D. ii. Ar1 the parts are compulsory.
Draw labelled diagrams where evernecessary.
E.
RDPUCPA
11' Differentiatebetweorgametogenesisandembryogenesis.
12 '
What are parthenocarpic fruits give example. t : wtrat
is back cross? Why is it done?
Draw
X 2 : l0
ik
14.
PART. C
ia
III.
15'
17 . Expand LAB. Mention two benefits
ofLAB?
8' Define resfriction endonucleases? Name the first restiction endonuclease discovered?
19.
Whatis fertilization?Explainitstypes?
5X3=15
.p
ed
20
PART. D SECTION.I
Answer any four of the following.
27 . with aneat labeiled diagram exprain seven
cefled eightnucreate femarqgametophyte.
28' Whatis spermatogsnesis explainwiththehelp ofsctematicrepresentation.
29 ' (a) what is contaception? (b) Mention
different catogories olcontaceptive methods.
(c\B-x1\u'srtsrl\$rsttre{Ns{s.
W.
30.
32.
5:20
SECTION - II
Answer any three of the following.
33. Draw aneatlabelleddiagramoffemale-reproductivesystem.
34. Describe the doublehelical model ofD.N.A.
35. a) what is sewage? b) Describe the secondary teatrnent of seawage.
36. Explain the salient features ofcloning rector.
37. Highlightanyfiveadvantagesofgeneticallymodifiedorganisms.
***t*****
3X5:15