Name: Nasrin Akter Mukta
Faculty of Veterinary Science
Bangladesh Agricultural University
 What is semen?
 Why it is necessary to examine semen?
 Semen evaluation.
 Semen is the liquid cellular suspension
containing spermatozoa and seminal plasma.
Why it is necessary to examine
semen?
1.For examination of breeding soundness,
infertility, artificial insemination and parasitic
diseases.
2.Semen quality of the first ejaculate after a long
period of sexual rest may have a lowered motility
and an increased number of dead spermatozoa.
Macroscopic Examination
1. Volume
2. Color
3. Consistency/density
4. Presence of foreign material
5. Gross motility
Microscopic Examination
1. Mass activity
2. Individual motility
3. Concentration estimation
4. Live and dead sperm estimation
5. Abnormal sperm estimation
Normal volume of semen in different animals-
1. Bull: 2-10ml (4)
2. Stallion: 30-250ml (70)
3. Ram/Buck: .5-1.5ml (1)
4. Boar: 150-500ml (250)
5. Dog: 1-25ml (10)
6. Cat: .01-.12ml (.04)
Colour Abnormal due to
1.Brownish------------ Orchitis
2.Dark red to pink----- Hemorrhage in male
reproductive tract
3.Yellow green-------- pus formation,
infection
4.Light brown---------- Contamination with
dung
5.Yellow-------------- Presence of urine
6.Curdy appearance----- Infection
Grade:
Thick creamy------------- Excellent
Thin creamy-------------- Very good
Thick milky---------------- Good
Thin milky----------------- Fair
Watery------------------ Extremely poor
 From animals- dung, pus , urine, hair, dust
 From environment- sand, bedding
materials, insects
 From AV- water, lubricant jelly, dust,
powder
Percentage of spermatozoa moving
progressively forward over the field in the
microscope at 20-40X under the coverslip.
Good semen------------60% motility
Excellent semen--------- 80%motility
.
Subjective estimation and graded as:
+ =no mass activity
++ =slow wave motion
+++ =rapid wave motion with formation of
eddies at the end of waves
++++ =distinct eddies
1.Haemocytometer technique: Semen is diluted
with water=1:100 to1:400 depending on the
species.
2.Photometric technique: Semen is diluted
with NaCL=1:100 to 1:400 depending on the
species.
3.Karrus scale technique: Semen is diluted
with normal saline=1ml in 9ml saline.
Semen Evaluation
Semen Evaluation

Semen Evaluation

  • 1.
    Name: Nasrin AkterMukta Faculty of Veterinary Science Bangladesh Agricultural University
  • 2.
     What issemen?  Why it is necessary to examine semen?  Semen evaluation.
  • 3.
     Semen isthe liquid cellular suspension containing spermatozoa and seminal plasma. Why it is necessary to examine semen? 1.For examination of breeding soundness, infertility, artificial insemination and parasitic diseases. 2.Semen quality of the first ejaculate after a long period of sexual rest may have a lowered motility and an increased number of dead spermatozoa.
  • 4.
    Macroscopic Examination 1. Volume 2.Color 3. Consistency/density 4. Presence of foreign material 5. Gross motility
  • 5.
    Microscopic Examination 1. Massactivity 2. Individual motility 3. Concentration estimation 4. Live and dead sperm estimation 5. Abnormal sperm estimation
  • 6.
    Normal volume ofsemen in different animals- 1. Bull: 2-10ml (4) 2. Stallion: 30-250ml (70) 3. Ram/Buck: .5-1.5ml (1) 4. Boar: 150-500ml (250) 5. Dog: 1-25ml (10) 6. Cat: .01-.12ml (.04)
  • 8.
    Colour Abnormal dueto 1.Brownish------------ Orchitis 2.Dark red to pink----- Hemorrhage in male reproductive tract 3.Yellow green-------- pus formation, infection 4.Light brown---------- Contamination with dung 5.Yellow-------------- Presence of urine 6.Curdy appearance----- Infection
  • 9.
    Grade: Thick creamy------------- Excellent Thincreamy-------------- Very good Thick milky---------------- Good Thin milky----------------- Fair Watery------------------ Extremely poor
  • 10.
     From animals-dung, pus , urine, hair, dust  From environment- sand, bedding materials, insects  From AV- water, lubricant jelly, dust, powder
  • 11.
    Percentage of spermatozoamoving progressively forward over the field in the microscope at 20-40X under the coverslip. Good semen------------60% motility Excellent semen--------- 80%motility
  • 12.
  • 14.
    Subjective estimation andgraded as: + =no mass activity ++ =slow wave motion +++ =rapid wave motion with formation of eddies at the end of waves ++++ =distinct eddies
  • 15.
    1.Haemocytometer technique: Semenis diluted with water=1:100 to1:400 depending on the species. 2.Photometric technique: Semen is diluted with NaCL=1:100 to 1:400 depending on the species. 3.Karrus scale technique: Semen is diluted with normal saline=1ml in 9ml saline.