eChapters

Community

1. A community is a group of people, who live in a geographical area and have an interest in each other for the purpose of making a living. It is a form of social organization existing between the family and state.
2. The people with common interests living in a particular area
3. An interacting population of various kinds of individuals (as species) in a common location
4. A group of people with a common characteristic or interest living together within a larger society

Introduction

What is community development?

Community development refers to the process of bringing community people together after identifying issues related to them and taking a collective action. Community development empowers residents and builds stronger, more integrated communities. Community development is an all-encompassing approach based on the ideas of empowerment, human rights, inclusiveness, social justice, self-determination, and collective action (Kenny, 2007).

COMMUNITY DEVELOPMENT (CD)

Meaning of Community Development

Community development is an exclusive term. It is used frequently to encompash every efforts towards the advance of community interest.

Community

A community is a group of people who live in a particular geographical area and have an interest on each other and have a purpose of making a living.

Development

It means growth or maturation. It is gradual and sequencial phases of changes. Example: Life from child to death

Definition of Community Development

1. It is bringing forth the potential abilities and qualities of a group of people who live together in a common territory or region and who have an interdependent relationship with each other.

2. Community Development is a continuous process of social action by which the people of community do the following things.

(a)   Define their common and group needs.

(b)   Organize themselves formally and informally for democratic planning and action.

(c)   Make group and individual plans to meet their need and solve their problems.

(d)   Execute their plans with maximum reliance upon their own resources.

(e)   Supplement their resources from outside community when necessary with services and materials.

3. Carl Taylor’s Definition

Community Development is a method by which people in villages are involved in helping to improve their own economy through their own effort. Thereby, they are effective working groups in the programme or national development.

ABSTRACT

Information and Communication Technologies (ICTs) are for everyone and that does not mean for urban or rural communities. Recent developments in the fields of information and communication technology are indeed revolutionary in nature. By definition, Information and Communication Technologies (ICTs) are a diverse set of technological tools and resources to create, disseminate, store, bring value-addition and manage information. Knowledge thereby becomes the fundamental resource for all economic and developmental activities in the knowledge society, of which rural poor form an equal part. The process of synthesis of knowledge possessed across communities with the global pool of knowledge and with the scope for further enrichment provides the genesis for information sharing.

The analysis of community mobilization in natural farming requires a systematic framework that captures the complex dynamics of agricultural transformation, social change, and community empowerment. This framework serves as a lens through which to examine successful cases of natural farming adoption while identifying the critical factors that enable communities to transition from conventional agriculture to sustainable practices. Understanding these dynamics is essential for replicating successful models and scaling natural farming initiatives across diverse contexts and geographies. Contextual analysis forms the foundation of any case study framework, requiring comprehensive understanding of the social, economic, environmental, and political conditions that influence community receptivity to natural farming practices. This includes examination of agricultural history, farming traditions, economic pressures, environmental challenges, and existing social structures that shape how communities respond to new agricultural app

The transformation of communities through collective action requires systematic approaches that can navigate the complexities of human behaviour, social structures, and environmental contexts. Community mobilization, while grounded in universal principles of participation and empowerment, manifests differently across various settings and circumstances, necessitating flexible yet structured processes that can adapt to local conditions while maintaining effectiveness. This chapter examines the intricate processes and diverse models that guide community mobilization efforts, with particular attention to rural contexts where unique challenges and opportunities shape the mobilization landscape

ABSTRACT

The role of community radio has been conceptualized as an important and powerful tool for informing, educating, entertaining and influencing the masses. Community Radio Station at KVK, Barh, Patna has brought about useful contributions to the farmers of surrounding villages and broadcasting different programmes related to agriculture, health, hygiene, nutrition and entertainment in the local language. Present study was carried out to see the impact of organic farming related talks. We found it a very effective tool to communicate with small and marginal farmers of surrounding villages for delivering useful information related with agriculture and organic farming.

Key words: Community radio, farmer, villages, organic farming information

The importance of science and technology (S&T) to rural societies has long been recognized. Despite the significant advancements in S&T in India since 1947, there remains an urgent need to deliver these advancements to the most underserved populations, enabling them to meet the challenges of an increasingly technologically sophisticated world. Technological progress continues to generate new methods of communication and information management, profoundly impacting society. These advancements offer unprecedented opportunities and challenges for scientific endeavors.

While science possesses a universal character, its application is influenced by local customs and values, especially in rural areas where behavior patterns and practices are deeply rooted in traditional beliefs and superstitions. These are not easily displaced by modern scientific approaches. Therefore, S&T policies for rural development must consider the local environment to effectively deliver the benefits of S&T to rural societies. This consideration is crucial for the management of rural natural resources and the environment.

Introduction

The concept of communication for development emerged with the Modernization theory, which developed its roots after World War II. Wilbur Schramm and Daniel Lerner, the two major proponents of this theory opined that the major obstacle to development was the psychology of the undeveloped citizens. The communication models under modernization paradigm observed communication process as the transfer of message from sender to receiver (Lasswell, 1948). It was found that communication theories like two step-flow, diffusion theory, or the early extension approaches were quite harmonious with the top-down modernization theory. After the Modernization paradigm, an another theory of communication for development emerged named as Dependency theory. Dependency theorist like Jean Servaes (1996) criticized the broadcasting and other mass-media systems as they tended to support modernization and were anti-development; also they were inclined to promote the political agenda. Solution to underdevelopment of third world countries require major changes in media structure that were dominated by commercial principles & foreign interests into media structures which are self-reliant and community oriented (Servaes, 2002). In 1970s scholars such as Paulo Freire and Nora C. Quebral started pleading in favour of bottom up development theories which led to evolution of a new development paradigm called the multiplicity paradigm. This paradigm conceptualised the basic idea that development is integral, multidimensional and dialectic process which can differ from one society to another (Okigbo and Eribo, 2004). Multiplicity paradigm led to emergence of a new form of communication called participatory communication.

Journal Citation Reports (JCR) and SCImago Journal Rank (SJR) are widely used metrics for evaluating journal impact. While JCR is based on Web of Science and emphasizes high-impact journals, SJR uses Scopus data, offering broader geographic and disciplinary coverage. This chapter evaluates their relative strengths and weaknesses, focusing on their applicability across disciplines and geographies. Multiple trends also impact research landscapes across the globe (Fig. 3.1).
Comprehensive tables provide a comparative overview of which metric is more suitable for various disciplines and global regions. The assessment of academic journals plays a critical role in research evaluation, academic promotions, and funding decisions. Two prominent journal-ranking systems, JCR and SJR, serve as benchmarks for these purposes. JCR, managed by Clarivate Analytics, primarily focuses on citation frequency over a two-year window. Conversely, SJR, developed by SCImago using Scopus data, incorporates a prestige-weighted citation approach over a three-year period (Fig. 3.2). Several of our Indian Scientific Journals are not covered by JCR. As more than 80 per cent Journals are from Europe and North America. The CLARIVATE covers only few Indian Journals most of which are published by Central Government Agencies

Horse

The visceral branches of the abdominal aorta are the coeliac, cranial mesenteric, renal, caudal mesenteric and testicular or ovarian.

The coeliac artery in horse is shorter than that in ox. It arises from ventral surface of the aorta and reaches the dorsal surface of the pancreas where it divides into three branches, the left gastric, hepatic and splenic.

The left gastric artery passes ventrally and cranially in the gastrophrenic ligament, gives off pancreatic and oesophageal branches and divides dorsal and caudal to the cardia into parietal and visceral branches. The parietal branch crosses the lesser curvature of the stomach just to the right of the cardia and ramifies on its parietal surface. The visceral branch is distributed in the similar manner on the visceral surface of the stomach. A long but narrow oesophageal branch arises from the parietal branch of the left gastric, passes cranially through the hiatus oesophageus and enters the thoracic cavity dorsal to the oesophagus and anastomoses with the oesophageal branch of broncho-oesophageal artery.

The hepatic artery is larger than the left gastric. It passes dorsal to the pancreas and reaches medial to the portal vein, divides into right and left branches from which the terminal branches enter the liver through portal fissure. Its collateral branches are the pancreatic, right gastric and the gastroduodenal arteries. The gastroduodenal artery further divides into right gastroepiploic and the cranial pancreaticoduodenal arteries.

Horse

The shoulder joint of horse has same features as those of ox. However, this joint in horse exhibits greater degree of mobility.

The elbow joint of horse is almost similar to that of ox except that there is only one interosseous ligament in horse against two in ox.

The carpal joint of horse has only minor differences from that of ox. The special feature of the joint in horse is that it has two additional ligaments, the superior check ligament and the inferior check ligament. The superior check ligament starts from the rough elevation on the distal third of the caudal surface, close to the medial border of the radius and is inserted to the tendon of superficial digital flexor above the carpus. The inferior check ligament is the continuation of the caudal (palmer) capsular ligament of the carpus. It joins the tendon of deep digital flexor at about midway on the palmer surface of the metacarpus. The check ligaments assist the tendons of flexor muscles of the digits after severe exertion to keep then tight and prevent flexion.

Horse

Articulations of bones of skull

Most of the joints of the bones of skull are sutures similar to those in ox. However, in the adult horse many of the sutures are effaced. The ossification of the cartilage between the basilar part of the occipital and the sphenoid occurs quite earlier. The fusion of the mandibular symphysis takes place at about second to third month after birth. The temporomandibular articulation has an additional ligament which consists of elastic tissue. It connects the post-glenoid process to the caudal border of the ramys of the mandible.

Hyoidean articulations

In the hyoidean articulations, there is only one intercornual articulation in horse instead of the proximal and distal cornual articulations appearing in the ox. The middle cornu is generally lodged in the articulation between the great and small cornu.

Horse

The hip joint has an additional ligament called the pubio-femoral ligament. It arises from the prepubic tendon, passes dorsally and laterally and then caudally and lodges into the subpubic (pubio-femoral) groove, penetrates the capsular ligament, passes through the acetabular notch and is inserted into the fovea capitis behind the round ligament on the head of femur. This ligament is peculiar to solipeds and it prevents the side kicking. The absence of this ligament in ruminants allows them abduction freely and that is how the ruminants can kick sideways. As against this, the equines can kick only back way. The other difference about the hip joint in horse is that the cotyloid ligament is narrower because of the deeper acetabulum.

The stifle joint of horse in general resembles that of ox except that the middle patellar ligament is not so prominent as that in ox.

The tibio-fibular articulation in horse is a diarthrosis and an amphiarthrosis. The diarthrosis is formed between the lateral condyle of tibia and the head of the fibula. It has intimate capsular ligament. The amphiarthrosis is formed between the shafts of the tibia and the fibula. The shafts of the two bones are binded by the proximal and distal interosseous ligaments.

The hock joint of horse has minor differences with those of ox owing to the difference in the number of tarsal bones and their arrangement. The synovial membrane is supported everywhere except at the dorsomedial (craniomedial) aspect where it bulges out in the cases of bog-spavin. If there is a distension of tarsal sheath, it bulges out as two rounded swellings on either sides of the tendon of deep digital flexor. The movements at the hock joint are very limited.

Horse

The arteries of fore limb of horse are more or less similar in their course and distribution. However, there are some special features in respect of some of these arteries as described below.

The brachial artery descends vertically on the medial aspect of humerus to its distal extremity, crosses it obliquely and descends along the joint capsule and medial lateral ligament of elbow joint, gives off common interosseous artery at the proximal third of the forearm and then continues distally as median artery.

The median artery descends along the caudomedial aspect of the radius covered by flexor carpi radialis muscle and divides just proximal to medial condyle into radial and collateral ulnar (ulnar) arteries.

The collateral ulnar artery is smaller of the two terminal branches of median artery. It descends along the cranial surface of radius under cover of the extensor carpi radialis and terminates a little above the carpus by anastomosing with a branch of radial artery.

Arteries

Horse

The common carotid artery in horse has a similar origin, course and distribution as that in ox except that it has no relation with the internal jugular vein since this vein is absent in horse. Each common carotid artery at its termination in front of the digastricus gives out internal carotid artery in horse in addition to the occipital and pharyngeal arteries given off by the common carotid artery in ox.

The internal carotid artery which is absent in ox is present in horse. It is considered as chief source of blood for the brain in horse. It passes over the guttural pouch and enters the cranial cavity through the foramen lacerum and gains the cavernous sinus. The internal carotid arteries of the opposite sides are connected by a large transverse branch called the intercarotid artery that lies behind the pituitary gland (further course of this artery will be described with the blood supply of the brain in horse).

The external carotid artery which is a direct continuation of the common carotid artery after its termination in front of the digastricus muscle is related to guttural pouch during its course along with other structures described in ox.

Horse

The arteries of the hind limb of horse have in general similar architecture as that of ox except the special features mentioned below.

The deep circumflex iliac artery which is a branch of the external iliac artery in ox has a variable origin in horse. It may originate directly from the aorta or the common iliac trunk just prior to the origin of the external iliac artery. The prepubic and deep femoral arteries arise either by a common trunk or separately from the femoral artery. The obturator artery is a well developed independent branch of the femoral artery in horse as against its origin as a branch of deep femoral artery in ox. The saphenous artery is a small branch of femoral artery and it supplies the skin on the medial aspect of the thigh and leg. The popliteal artery terminates by its division into cranial and caudal tibial arteries at a lower level in horse than that in ox. The caudal tibial artery is larger and longer in horse than that in ox. From the proximal plantar arch extend four caudal metatarsal arteries instead of four, two of them are superficial and the other two deep branches. The large metatarsal artery descends along the groove between the large and lateral small metatarsal bone and divides just above the fetlock into lateral and medial digital arteries. Each digital artery divides at the middle of the wing of the third phalanx into preplantar and plantar digital arteries. The preplantar digital arteries supply the sensitive laminae of the sole. The plantar digital arteries of the opposite sides form anastomosis. Small laminar branches from the anastomosis form the circumflex artery of the toe which supplies branches to the sole.

Arteries of thorax

Horse

The bronchial and oesophageal arteries in horse have a common trunk of origin as broncho-oesophageal artery. It arises from the convexity of aortic arch, passes ventrally and caudally on the right side of the aorta and divides into bronchial and oesophageal arteries. The oesophageal artery passes caudally in the caudal mediastinum along the dorsal face of oesophagus and supplies branches to oesophagus, caudal mediastinal lymph nodes and pleura and anastomoses with the pleuro-oesophageal branch of the gastric artery.

The intercostal arteries are eighteen pairs in number. The first pair arises from the superior artery, the next three pairs come from subcostal artery and the remaining four arise from the thoracic aorta.

The phrenic arteries are not variable in origin as in the ox. They are small and are two to three in number. They arise on the ventral face of the aorta while it passes through the hiatus aorticus and enter the crura of the diaphragm.

The rest of the arterial branches of thorax in horse are similar to those in ox.

Stomach

Horse

The stomach of horse is a simple stomach. It is ‘J’ shaped sac with its right part very much shorter than the left part. It is situated in the dorsal part of the abdominal cavity behind the diaphragm and liver mainly to the left of the median line. The parietal surface faces craniad and dorsad and to the left. It is related to the diaphragm and liver. The visceral surface faces caudad and ventrad and to the right. It is related to the small intestine and colon. Its lesser curvature is short and the greater curvature is extensive. The left extremity is called the saccus caecus. It lies ventral to the sixteenth or seventeenth rib. It is related to pancreas and terminal part of greater colon caudally and to the base of the spleen laterally. The right extremity is the pylorus. It is smaller and is continued by duodenum. The stomach is fastened by several ligaments which include the gastro-phrenic ligament, the gastro- pancreatic ligament, the greater omentum, the lesser omentum and the gastro-splenic ligament. The capacity of the equine stomach is about 8 to 15 liters.

The wall of the stomach consists of four coats, the serous, muscular, submucous and the mucous. The mucous membrane is clearly divided into two parts by sinuous ridge called the margo plicatus. The part which is towards the left extremity is nonglandular while that towards the right extremity is glandular.

Horse

The ovaries in mare are bean shaped and much larger than those of cow. Each is about 7 to 8 cm long and about 3 to 4 cm thick. It weighs about 70 to 80 gm. These are situated in the sublumbar region under the fourth or fifth lumbar vertebra. They are usually in contact with the roof of the abdomen. The average distance of ovaries from the vulvar orifice is about 50 to 55 cm in the average sized mare. The notch on the free border leads to a depression, the ovulation fossa where ovulation occurs.

The uterine tubes are shorter and more flexuous in mare than those in cow. Each is about 20 to 30 cm long. At its ovarian end it is wider with a diameter of about 4 to 8 mm and becomes narrower at its uterine end with a diameter of about 2 to 3 mm.

The uterus in mare is situated partly in abdomen and partly in pelvis. The horns of the uterus are usually pressed against the sublumbar muscles by the intestine. When moderately distended they are about 25 cm long. The junction of the uterine horns with the body of the uterus is abrupt. The average length of the body is about 18 to 20 cm and its diameter is about 10 cm when moderately distended. The cervix is about 5.0 to 7.5 cm in length and 3.5 to 4.0 cm in diameter. The cervical canal is straight. The mucous membrane of the uterus has no cotyledons.

The vagina in mare is shorter than that in cow. It measures about 15 to 20 cm in length and 10 to 12 cm in diameter when slightly distended. Most of the vagina is retroperitoneal.

Horse

In addition to the common articulations of vertebrae, the lumbar region of horse has two special articulations, the inter-transverse articulations and lumbosacral articulations.

The intertransverse articulations are bilateral joints formed between the transverse processes of the fourth and fifth and between the fifth and sixth lumbar vertebrae. The articular surfaces of these joints are the oval facets on the transverse processes of these vertebrae, the cranial ones being concave while the caudal ones the convex. These are synovial joints (diarthrodial). The capsule of the joint is reinforced ventrally.

The lumbosacral articulations are diarthrodial joints formed between the transverse processes of the sixth lumbar vertebra and the wings of the sacrum. These joints are similar to the intertransverse articulations.

The sacroiliac articulation of the pelvis is similar to that of ox. However, the sacrosciatic ligament is broader. Its lateral surface is related to middle gluteus, biceps femoris and semitendinosus muscles.

Horse

Lymph nodes of the wall of abdomen and pelvis

The lumbar aortic lymph nodes extend from kidneys to the deep circumflex iliac vessels. These are not clearly distinguishable from the cranial and caudal mesenteric, renal, testicular or ovarian, uterine and iliac lymph nodes.

The internal iliac lymph nodes are placed at about the origin of the iliac arteries. The external iliac lymph nodes are several small nodes situated in the triangular space between the cranial and caudal branches of the circumflex iliac artery.

The deep (internal) inguinal lymph node is not abdominal in position. It is not situated at the pelvic brim. It is one of the group of the lymph nodes of the hind limb.

The superficial (external) inguinal lymph nodes are on either side of the penis and in front of the superficial inguinal ring in male and above the mammary glands as the supramammary lymph nodes in female.

The prefemoral lymph nodes are about a dozen small glands arranged in an elongated mass placed on the medial aspect of the cranial border of tensor fasciae lata and on the caudal branch of circumflex iliac artery.

Horse

The testicles in horse are oval in form and they are comparatively smaller in size than those in ox. The long axis of the testicles is parallel to the body of the animal and hence the attached border of the testicle is dorsal while its free border is ventral in position inside the scrotum. The testicle of the stallion is about 10 to 12 cm long, 5 cm wide and about 6 to 7 cm thick. It weighs about 225 to 300 gm. The size of the left and right testicle varies and the left testicle is often larger than the right one.

The epididymis is adhered to the attached (dorsal) border of the testicle. The rest of the features of epididymis in horse are similar to those of ox.

The vas deferens of horse right from its origin from the tail of epididymis to its course up to the dorsal surface of the bladder it has a uniform diameter of about 6 mm. Thereafter, it forms a fusiform enlargement, the ampulla of the vas deferens and beyond the ampulla the duct abruptly reduces in size. The ampulla is about 15 to 20 cm long and its diameter is about 2 cm. The genital fold is wider and hence the two ducts apart from each other. The vas deferens and the duct of seminal vesicle open in a common ejaculatory orifice on each side of the colliculus seminalis.

Horse

The muscles of lumbar spine in horse are more or less similar to those of ox. Of the sublumbar muscles, the psoas minor lies under the bodies of the lumbar and last three thoracic vertebrae. It arises from dorsal ends of sixteenth and seventeenth ribs and eighteenth thoracic vertebra and the first five lumbar vertebrae.

The psoas major arises from dorsal ends of last two ribs and the ventral faces of the transverse processes of the lumbar vertebrae. It is much wider than that of ox and covers the quadratus lumborum entirely.

The origin of iliacus muscle is limited to sacrum and ilium only. It has no lumbar origin and it is not so intimately united with psoas major muscle.

The quadratus lumborum is less developed.

The intertransversarii lumborum is absent between the fifth and sixth lumbar transverse processes.

The muscles of abdominal wall in horse do not have any striking differences, except that the obliquus abdominis externus is thicker and more extensive. The muscular portion of this muscle reaches the external angle of ilium and as high as lumbar transverse processes.

Horse

The muscles of shoulder region namely the supraspinatus, infraspinatus, teres major, teres minor and coracobrachialis in horse resemble those of ox. The subscapularis muscle has only a single head of origin in horse as against three heads in ox. The deltoideus muscle has two parts of origin as that of ox but in horse its acromial part is named as cranial part and it arises from scapular spine and the scapular fascia instead of the acromion process. In addition to these muscles, the shoulder in horse is composed of one more muscle named as capsularis. The capsularis is a very fine narrow muscle arising from the caudal part of the rim of the glenoid cavity of scapula and is inserted on the caudal part of the neck below the head of the humerus by insinuating itself between the fibres of brachialis muscle. This muscle is peculiar to solipeds and it raises the capsular ligament of shoulder joint during flexion of the joint.

The muscles of arm in horse are in general similar to those of ox except the following minor differences. The tendon of origin of biceps brachii is adapted to the intertuberal (bisipital) groove. The tensor fasciae antibrachii is thin in front and wide below. The medial head of triceps brachii is less developed and extends from the middle of the medial surface of shaft of humerus. The anconeus is smaller and less voluminous.

Amongst the muscles of forearm and manus, the flexors of carpus especially the flexor carpi radialis, flexor carpi ulnaris and the ulnaris lateralis resemble those of ox. The pronator teres is either vestigial or completely absent. The medial digital extensor is absent. The extensor carpi radialis resembles that of ox. The common digital extensor arises in common with the extensor carpi radialis. Its tendon descends over the synovial capsule of the carpus, passes down the metacarpus and at the fetlock it receives two slips from suspensory ligament to form the broad ligament which is inserted to the pyramidal extensor process of the distal phalanx. The lateral digital extensor is smaller. It arises from humerus and radius. Its tendon is inserted to the prominence on the dorsal (cranial) aspect of the proximal extremity of the proximal phalanx. The extensor carpi obliquus is inserted to the head of the medial small metacarpal bone. The superficial digital flexor does not divide into two parts. Its tendon is reinforced above the carpus by a strong fibrous band- the superior check ligament. The ring for the deep digital flexor is formed entirely by the tendon of superficial digital flexor. The deep digital flexor has same heads of origin as those of ox. Its tendon receives about half way down the metacarpus the inferior check ligament. It is inserted to the semilunar crest and tendinous surface of the distal phalanx.

Horse

The cutaneous muscle in horse is thin and incompletely developed in the superficial fascia. The cutaneous muscle of the facial region (cutaneous fasciei) is incomplete and poorly developed over the mandibular space and the massetor muscle. Rostrally it passes to the angle of the mouth and blends with the orbicularis oris. The cutaneous muscle of the cervical region (cutaneous colli) is situated along the ventral region of the neck.

The frontalis muscle is absent.

The orbicularis oris forms incomplete ring around the rima oris. The levator nasolabialis is less extensive and is divided into the superior and inferior branches. Between the two branches pass the dilator naris lateralis and levator labii superioris. The levator labii superioris extends from malar, lacrimal and the maxillary bones to the upper lip in a common tendon with the muscle of the opposite side. The zygomaticus is thin, short and weak. It arises from the fascia covering the massetor. The incisivus maxillaris muscle which is absent in ox exists in horse and it lies under the mucous membrane of the upper lip. It originates on the alveolar border of the incisive bone from the level of lateral incisor to the first premolar and it inserts to the upper lip. Its action is to depress the upper lip. The incisivus mandibularis which is also absent in ox exists in horse under the mucous membrane of the lower lip. It originates at the alveolar border of the body of the mandible from the level of lateral incisor to the first premolar and is inserted on the skin of the lower lip and the chin. Its action is to raise the lower lip. The incisivus maxillaris and the incisivus mandibularis muscles acting together cause the closing of rima oris. The depressor labii inferioris is thicker and extends further back. The buccinator is almost similar to that of ox.

Horse

The tensor fasciae latae is less extensive.

The superficial gluteus exists separately. It is ‘V’ shaped. It originates from the lateral angle of ilium (tuber coxae) and gluteal fascia and is inserted to the third trochanter. The middle gluteus is the largest of the three gluteal muscles and is very extensive. It originates from the aponeurosis of the longissimus dorsi, extends as far forwards up to first lumbar vertebra and is inserted in three heads, to the trochanter major, the crest ventral to trochanter major and the trochanteric ridge. The deep gluteus is smaller than the middle gluteus and is inserted to the convexity of the trochanter major.

The biceps femoris has an additional insertion to the femur on the rough surface near the trochanter tertius.

The semitendinosus arises from the transverse processes of the first two or three coccygeal vertebrae. The semimembranosus is larger and arises from the sacrosciatic ligament also.

The sartorius does not arise from the shaft of the ilium. The gracilis is not so extensively fused to its fellow at the origin.

The obturator internus has an iliac part- the pisiformis. Its tendon passes through the lesser sciatic foramen and hence does not unite with that of the obturator externus.

Articularis genu is absent

Horse

The fascia in the cervical region of horse has two layers, the superficial and deep. Each of these is also double layered. The superficial fascia contains the cutaneus muscle the cutaneus colli. The fascia of the two sides meets at the median line along the nuchal ligament and ventrally at the fibrous raphe.

The brachiocephalicus is undivided. It arises from the mastoid process, nuchal crest and wing of the atlas and the transverse process of the second, third and fourth cervical vertebrae. The sternocephalicus is also undivided. It arises from the cartilage of the manubrium sterni and inserts at the angle of the lower jaw. The dorsal border of this muscle forms the ventral border of the jugular furrow. The sternothyrohyoideus muscle consists of two separate but unequal parts, the sternothyroideus and the sternohyoideus. The sternothyroideus is and the sternohyoideus is larger. The first part inserts on the thyroid cartilage of the larynx and the second part inserts to the body of the hyoid bone. The omohyoideus is more extensive in horse than that in ox. It arises from the subscapular fascia near the shoulder joint and inserts at the body and the lingual process of the hyoid bone. The scalinus has two parts like those of ox, but the dorsal part in horse is smaller. It arises on the transverse process of the seventh cervical vertebra and inserts on the first rib. The ventral part is very extensive. It arises from the transverse processes of the third to sixth cervical vertebrae and inserts on the medial surface of the cranial border of the first rib. The longus capitis (rectus capitis ventralis major) arises from the transverse process of third, fourth and fifth cervical vertebrae and is inserted on the tubercle at the junction of basilar part of occipital bone with the basi sphenoid. It does not form aponeurosis either at the origin or at its insertion. The rectus capitis ventralis (rectus capitis ventralis minor) is smaller in horse than that in ox. The intertransversarii cervicis (intertransversalis colli) are smaller and present six fasciculi. The most cranial of these is separated from the common mass formed by the rest of these fascicles.

Muscles of the back (spine), muscles of thorax and muscles of thoracic girdle of Horse, Dog, Sheep and Goat, and Pig almost resemble those of ox except for a few miner differences due to variations in the number of bony segments of the vertebrae, ribs and sternebrae.

Fowl

Muscles of back (spine)

Spinalis thoracis is the thoracic part of the spinales complexus. It originates by aponeurosis on the spinous processes of the thoracic vertebrae including the dorsal median ridge of the synsacrum, dorsal surface of the bases of the transverse processes and the cranial border of the ilium. The muscle inserts by multiple tendinous slips on the spinous processes, vertebral arches, transverse processes of several thoracic vertebrae and the vertebral ribs. This muscle helps in straightening of the head and neck of the fowl.

Iliocostalis et longissimus dorsi is the segmented muscle originating on the transverse processes of the thoracic vertebrae and inserting on the vertebral parts of the ribs. This muscle assists in elevating the thorax.

Horse

There are six pairs of lumbar, five pairs of sacral and five pairs of coccygeal spinal nerves in horse. Their origin, course and distribution is in general similar to those in ox.

The number of sympathetic lumbar and coccygeal ganglia is just the same in horse as that of ox. However, the number of sacral sympathetic ganglia is four in horse as against five ganglia of ox.

The greater (major) splanchnic nerve in horse is formed by the fibres received from sixth or seventh to fourteenth or fifteenth thoracic sympathetic ganglia. It is smaller in its cranial thoracic part but as it proceeds caudally it gradually increases in size so much that it becomes larger than the thoracic sympathetic trunk in the caudal thoracic part. It receives a communicating branch from the lesser splanchnic nerve before terminating in the coeliacomesenteric ganglion.

The lesser (minor) splanchnic nerve is formed by fibres received from the last three or four thoracic and the first two lumbar sympathetic ganglia. It communicates with the greater splanchnic nerve and the renal and adrenal plexuses and terminates in the coeliac plexus and ganglion.

The rest of the features of spinal nerves and autonomic plexuses of the abdomen and pelvis in horse are almost similar to those of ox except those related to the distribution of fibres to the parts of ruminant versus simple stomach.

Horse

The brachial plexus in horse is formed by ventral branches of the last three thoracic and first two thoracic spinal nerves similar to that in ox. The disposition and distribution of nerve branches extending from the plexus is almost similar to that of the ox except the following two.

The radial nerve after reaching the musculospiral groove gives out a cutaneous branch that passes through the lateral head of triceps and is distributed to the skin on the lateral aspect of forearm.

The main trunk of the radial nerve after crossing the carpus descends along the medial aspect of the palmer surface of metacarpus as palmer medial metacarpal nerve and further down on the medial digit as palmer medial digital nerve.

The ulnar nerve descends the carpus and after reaching the metacarpal region joins the lateral branch of the median nerve, descends first along the lateral aspect of the palmer surface of metacarpus as palmer lateral metacarpal nerve and then along the lateral (abaxial) aspect of the lateral digit as palmer lateral digital nerve.

Horse

The optic and oculomotor nerves in horse are thinner than those in ox. The oculomotor nerve leaves the cranial cavity with the ophthalmic and abducent nerves through the orbital foramen and the trochlear nerve leaves the cranial cavity through a small foramen immediately above the orbital fissure in horse as against the foramen orbitorotundum in ox. The ophthalmic branch of the trigeminal nerve leaves the cranium through the orbital fissure, the maxillary branch through the foramen ovale and the mandibular branch through the foramen rotundum. As against this, the ophthalmic and maxillary branches in ox emerge through the foramen orbitorotundum and the mandibular branch through the foramen ovale. The lacrimal nerve, a branch of the ophthalmic, runs rostrad on the rectus dorsalis and levator palpebrae superioris and ramifies chiefly in the lacrimal gland and the upper eyelid. One of its branches communicates with the orbital branch of the maxillary nerve, penetrates the periorbita, gains the temporal region behind the supraorbital process, forms a plexus with the branches of the frontal and auriculopalpebral nerves and divides to distribute fibres to the skin of the temporal region. The continuation of the maxillary nerve as infraorbital nerve gives out the caudal maxillary alveolar and middle maxillary alveolar branches to supply the molar and premolar teeth and before emerging through the infraorbital foramen gives out the rostral maxillary alveolar branch for the incisor and canine teeth.

Horse

The lumbosacral plexus in horse is formed by last three lumbar and first two sacral nerves, similar to that in ox. The caudal gluteal nerve divides into two branches. The medial branch supplies the superficial gluteal muscle in addition to the middle and deep gluteal and biceps femoris muscles. The lateral branch reaches the level of tuber ischii and terminates into the semitendinosus muscle at the perineal region. The sciatic nerve is almost similar to that of ox in the disposition and distribution of its branches. The superficial and deep peroneal nerves are also similar to those of ox. The tibial nerve divides at the distal third of the leg into medial and lateral plantar nerves. Each plantar nerve divides at the fetlock into cranial, middle and caudal digital nerves.

Dog

The lumbosacral plexus in dog is formed by the last four or five lumbar and first two or three sacral nerves. The cranial gluteal nerve receives fibres from sixth and seventh lumbar and first and second sacral nerves. The caudal gluteal nerve arises from sixth and seventh lumbar and first sacral nerves. The sciatic nerve derives fibres from sixth and seventh lumbar and first and second sacral nerves. The lateral cutaneous nerve arises either from sciatic or from the peroneal nerve. The peroneal nerve divides into superficial and deep branches, similar to those of ox. The tibial nerve divides into medial and lateral plantar nerves at the level of distal third of the leg. The medial plantar nerve divides at the metatarsus into medial and lateral branches. The medial branch becomes the first plantar common digital nerve. It divides to form the plantar proper digital nerves of the first and second digits. The lateral branch divides into three plantar metatarsal nerves which unite, in the intermetatarsal space with the three plantar common digital nerves of the lateral plantar nerve. Each of these united plantar common digital nerves descends and after reaching at the metatarso-phalangeal articulation into three plantar proper digital nerves. The lateral plantar nerve, divides into three plantar common digital nerves which join the three plantar metatarsal nerves and form the plantar (caudal) proper digital nerves. The united proper digital nerves supply the second to fifth digit and terminate into the corresponding intermetatarsal space.

Horse

The lumbar vertebrae in horse are six in number. The bodies of these vertebrae are shorter. The first three of them have a distinct ventral spine which subsides thereafter. The transverse processes increase in length from first to third or fourth and then diminish. The first one or two slightly curve caudad and the last two or three curve craniad and the third is at right angles. The caudal border of the transverse process of the fifth vertebra at its base has an oval concave facet which articulates with a convex facet on the cranial border of sixth vertebra. The sixth transverse process is thick at the base and thin, narrow at its free end. It is curved forward. It has a large concave facet on its caudal border by which it articulates with the corresponding facet on sacrum.

The sacrum of horse is formed by the fusion of five sacral vertebrae similar to that in ox. However, the fusion of the spinous processes is incomplete. On either side of the base of the each spinous process is a groove which presents the dorsal sacral foramen. There are four foramina on each side of the dorsum of the sacrum of horse. The ventral surface of sacrum of horse is not so deeply arched as that of ox. The wings of sacrum are prismatic. Each wing has a large oval convex facet for articulation with similar facet on the caudal border of the transverse process of last lumbar vertebra.

The coccygeal vertebrae are eighteen to twenty in number in horse. The laminae of the neural arch of the coccygeal vertebrae beyond fourth vertebra fail to meet dorsally.

The pelvic bone (os coxae) of horse is in general similar to that of ox. The gluteal line on the gluteal surface of the ilium is faint. The ilium is placed more obliquely. The articular surface of ilium is rough and large and extends nearly to the external angle. The internal angles of the ilium of opposite sides are more close to each other. The external angles are formed of four tuberosities each.

The ischium of the two sides meets at a greater angle because of which the pelvic floor is bowl like. The ischial arch is wide and shallow. The ridge on the ventral surface of ischium is absent. The tuber ischii is not trifid. The lower border of tuber ischii forms the ventral ischiatic spine. The ventral surface of pubis is crossed by pubic groove which leads to acetabular notch that transmits the pubic femoral ligament.

Horse

The scapula of horse is a flat triangular bone placed at the shoulder region applied against the cranial part of the lateral wall of thorax similar to that in ox. The scapular spine is placed a little further caudad from the cranial border so that the proportion of the area of supraspinous to infraspinous fossa is one third to two third of the lateral surface of the scapula. The subscapular fossa is deeper and presents well marked vascular impressions. The nutrient foramen is placed at the distal third of the infraspinous fossa. The tuber scapulae and the glenoid cavity are placed further apart. The glenoid cavity is oval in outline and its rim has a distinct notch on its craniomedial aspect. The coronoid process is better developed and the acromion process is absent.

The humerus in horse is directed obliquely distally and caudally forming an angle of about 55 degrees with the horizontal plane almost equaling to that in ox. The musculospiral groove on the shaft is deeper and more spirally curved. The nutrient foramen is placed on the distal third of the medial surface. The deltoid tuberosity is better developed. The medial and lateral tuberosities of the proximal extremity are more prominent. The intertuberal (bisipital) groove is divided by an intermediate ridge. The summit of the lateral tuberosity does not arch inward. The head is smaller than that in ox. The coronoid and olecranon fossae of the distal extremity are shallower than those in ox.

The radius of the horse is larger and longer of the two bones of the forearm. Close to the medial border of the caudal surface in the lower third of the shaft is a rough elevation for attachment of the superior check ligament (an accessory ligament of the superficial digital flexor). The caudal surface of the shaft towards its lateral border presents a rough triangular area which tapers to a point in the distal third of this surface. This is for attachment of the ulna. The distal interosseous space is absent because the shaft of ulna is shorter and does not reach to the distal part of the shaft of radius. The grooves on the cranial surface of the distal part of the shaft are better marked. The radial tuberosity at the craniomedial aspect of the proximal extremity is larger and more prominent than in ox. The distal articular surfaces are not oblique. It presents two tubercles one on each side, for ligamentous attachment. The tubercle on the lateral aspect is grooved for passage of tendon of lateral digital extensor.

Horse

The skull of horse is also pyramidal in shape like that of ox but the base of the pyramid is less wide than that of the ox. It is shorter in length and narrower in width than that of the ox. The cranium is smaller externally, however, the cavity of cranium is larger than that of the ox. The nasal cavity is divided into two chambers by nasal septum. The floor of the nasal cavity is shorter and less concave than that of the ox. The left and the right nasal chambers are completely separated and do not communicate with each other. The horn core is absent.

The occipital bone is placed at the extreme caudal part of the skull, caudal condyloid foramen is absent, the basi occipital is longer and prismatic and the squamous occipital is crossed by a nuchal crest. The sphenoid bone has two parts, the pre and post sphenoid, as that in case of ox. The wing of the post sphenoid presents three notches, carotid, oval and spinosal for internal carotid artery, ventral maxillary nerve and spheno-spinous artery respectively. The foramen orbitale and the foramen rotundum are not united. There are no major differences in the ethmoid bone of ox and horse. The frontal bones are less expansive than those of ox. These are situated between parietals caudally and nasals rostrally. The supraorbital foramen perforates the root of the supra orbital process that joins the zygomatic process of the squamous temporal. The horn core is absent. The ventral borders of the frontal bones of the opposite sides form a projection which fits into the notch formed by the two nasal bones. The temporal bone in horse has three parts, the squamous, petrous and tympanic as against two parts, the squamous and petrous of the ox. The squamous part is much more developed than that of ox. It has three parts, the body, zygomatic process and the occipital (pyramidal) process. The later one arises from the caudal part of the squamous. The stylomastoid foramen is between the hyoid and the mastoid processes and the auditory bulla is smaller. The interparietal is a single bone as that of ox.

Horse

The femur of horse is more massive than that in ox. The proximal third of the caudal surface of shaft of femur presents a rough eminence for attachment of biceps femoris muscle. The trochanter minor is a rough ridge like structure. The proximal third of the lateral border of shaft presents trochanter tertius for attachment of superficial gluteus muscle. The trochanter major is comprised of a convexity, a summit and a crest. The trochanteric ridge is vertical and it connects the trochanter major with the third trochanter. The lateral supracondyloid crest and the supracondyloid fossa are better developed in horse than that in ox. The patella of horse is wider and longer than that of ox.

The tibia in horse is relatively longer than that in ox. The popliteal line is prominent. It extends from the proximal third of the medial border, obliquely crosses the caudal surface and ends at the middle of the lateral border of the shaft of tibia. The medial border in its proximal third bears a small popliteal tubercle for attachment of popliteus muscle. The lateral border is attached to the shaft of the fibula and encloses an interosseous tibiofibular arch with the fibula. At the proximal extremity, the cranial tuberosity is vertically grooved. The lateral condyle on its lateral side presents facet for articulation with the proximal extremity of fibula. At the distal extremity, the grooves are oblique. The lateral malleolus is fused with the distal extremity of tibia, The medial malleolus is more prominent than the lateral one.

Horse

The first cervical vertebra (atlas) of horse is more or less similar to that of ox with a few variations as below

The wings of atlas are curved ventrad and laterad. These are thinner than in ox but their borders are thick.

The wings present an additional foramen, the transverse foramen in the caudal part.

A faint groove on the ventral surface of the wing connects the transverse foramen to the intervertebral foramen.

Horse

The bony cage of thorax is longer but narrower in horse than that in ox. It is compressed laterally

The thoracic vertebrae are eighteen in number. Their bodies are shorter. The spinous process of the first one is shorter and it is curved backward. The height of the spinous process increases up to third and fourth and there after it diminishes gradually up to fifteenth beyond which it is almost same. The backward inclination of the spinous process is most pronounced in the second. The spine of the sixth vertebra is straightly vertical and that of the last two vertebrae is directed slightly forward.

The ribs are in eighteen pairs. First eight pairs are sternal and the remaining ten pairs are asternal. These are shorter, narrower and more curved. The length of the ribs increases up to sixth and then it diminishes. The cranial borders of the ribs from second to sixth are sharp and from ninth to eighteenth they are rounded and thick. The lower edges of the ribs are excavated for receiving the costal cartilages. The first rib inclines little forwards, the second rib is vertical and the rests slope backwards.

The first pair of costal cartilages articulates at their distal ends with each other and with the sternum. The upper ends of the cartilages form synarthroidial joints with the ribs.

The sternum of horse is composed of seven sternebrae. It is canoe or boat shaped and presents three faces, three borders and two extremities. It is compressed laterally in front and dorsoventrally behind. The dorsal surface is narrow and triangular. It is concave craniocaudally. The lateral surfaces are convex above and slightly concave below. The lateral borders separate the dorsal surface from the lateral surfaces and they give attachment to two lateral sternal ligaments. The ventral border is the direct continuation of the cariniform cartilage of the cranial extremity of the sternum. It is thin, sharp and convex from before backwards. It is very prominent and can be felt by palpation in live animal. It is also called as sternal crest or keel. The cranial extremity presents a laterally compressed cariniform cartilage which presents a deep notch dorsally for articulation with the first pair of costal cartilages. The first sternebra is fused with second and the manubrium is made up of cariniform cartilage and the first sternebra.

Mouth

Horse

The mouth cavity (cavum oris) of horse is longer and narrower. The vestibule of the mouth cavity is less capacious than that of ox.

Dog

The form and size of the mouth cavity vary greatly in different breeds of dog. In some breeds the mouth is long and narrow while in others it is short and wide. Rima oris in general in all types of dogs is extensive.

Sheep and Goat

The mouth cavity is elongated and narrow. The rima oris is short. The buccal vestibule is capacious but the labial vestibule is small.

The thoracic spinal nerves of the horse, dog, sheep and goat, pig and fowl almost resemble to those of ox in origin, disposition and distribution. The number of pairs of thoracic spinal nerves, however, vary and it corresponds to the number of thoracic vertebrae present in those particular species of animal.

Horse

The kidneys of horse slightly differ in form and size than those of ox. The outer surfaces of kidneys of horse are smooth and plane as against lobulated kidneys of ox. The right kidney is like the heart of the plying cards while left kidney is bean shaped. The right kidney is placed under the vertebral ends of the last two ribs and first lumbar transverse process. The left kidney is situated under the last rib and the first two or three lumbar transverse processes. The hilus of both the kidneys is at about the middle of the medial border of the respective kidneys. The cranial extremity of the right kidney is thicker while the caudal extremity of the left kidney is wider and thicker. The hilus of the kidneys lead into the renal sinus in the interior for the lodgment of the renal pelvis which is the dilated origin of the ureter. The inner central part of the medulla forms a concave ridge called the renal crest. It presents numerous openings through which the large ducts open into the renal pelvis. This part is called the area cribrosa.

The ureter of the horse kidney begins at the renal pelvis and is about 70 cm in length and 6 to 8 mm in diameter.

The urinary bladder of horse is shorter but wider than that of the ox. Its capacity is about 2.8 to 3.8 liters. The rest of the features are same as those of ox.

Horse

The caudal vena cava in horse is largely embedded in the substance of the liver on its diaphragmatic surface. Here its free surface is covered only by the peritoneum. After crossing the liver, the caudal vena cava continues caudally along the right side of the abdominal aorta. During its course it gives off several branches from the dorsal and lateral surface.

The lumbar veins (parietal) are five or six pairs in number. The last one or two of these often join the internal iliac veins.

The renal veins are thin walled. The right renal vein is shorter than the left one.

The phrenic veins are two or three in number. The circumflex iliac veins join either the caudal vena cava or the internal iliac vein.

The portal vein is formed by the union of cranial and caudal mesenteric and the splenic veins in the cranial part of the sublumbar region at about the level of second lumbar vertebra. It passes cranially and to the right of the median plane continues through the portal ring of the pancreas and reaches to the portal fissure of the liver. Before entering the portal ring of the pancreas, the portal vein receives right gastroepiploic vein, right gastric vein and cranial pancreaticoduodenal vein. The cranial mesenteric, caudal mesenteric and the splenic veins are formed by the tributaries from the veins which are satellites of the branches of the respective arteries. After its entry into the hepatic portal, the portal vein divides into three principal branches. These include the right branch for right lobe, the middle branch also for the right lobe and the left branch for the left and the quadrate lobe.

Lungs and pleura

Horse

The lungs of horse are comparatively larger and longer than those of ox. These are not divided into lobes by deep fissures. The surface markings of lobules of lungs are indistinct due to reduced amount of interlobular connective tissue. The upper part of the medial surface of left lung has two grooves which are the markings of the aorta and oesophagus. These markings are comparatively faint and less marked. The ventral border of both lungs presents cardiac notch. The left cardiac notch is quadrilateral and more extensive than the right one. It extends from third to sixth ribs. The right cardiac notch is smaller and triangular. It extends from third to fifth ribs.

Dog

The lungs of dog are short and wide in order to be accommodated in the correspondingly similar shape and size of the thoracic cavity of dog. The fissures in the ventral border of the lungs are deeper and extend up to the hilus of the lung giving it an appearance of independent lobes. The right lung has four lobes and the left lung has two lobes. The intermediate (accessory) lobe of the right lung presents on its lateral surface a groove for caudal vena cava and right phrenic nerve. The cardiac impression on the mediastinal surface of the cardiac lobe is deeper in the right lung than that in the left lung. The right cardiac notch is triangular and it lies at the level of fourth and fifth interchondral spaces. The left cardiac notch is more ventral in position at the level of fifth and sixth interchondral space. The lobules are small and the surface lobulation is not distinct because of less amount of interlobular connective tissue.

Objective: Explore and understand the key identical characteristics that differentiate the suborders Symphyta and Apocrita within the order Hymenoptera.

A. Answer the following question?

1.    Mention the factors which affect the chemical composition of green forage?

Ans: Soilcompositionandhealth,applicationofmanureandfertilizer, frequency of irrigation, stage of growth, frequency of cutting and variety of strain.

2.    How does the age of plant affect the chemical composition of forage?

Ans: As the plants advance in age, dry matter, crude fibre and ash increase whereas the crude protein and ether extract decreases.

3.    What is food?

Ans: This is the combination of materials that provides nutrients

4. What is feed?

Ans: It refers to the food but most commonly used to animal food.

5. What is diet?

Ans: It is defined as the mixture of feedstuffs used to supply nutrientsto anyindividual.

6.    Whether mineral content of feeds remain fixed?

Introduction

Agriculture is the primary source of livelihood for about 58 per cent of Indian population. Gross Value Added (GVA) by agriculture, forestry and fishing was estimated at Rs. 19.48 lakh crore in FY2020. Growth in GVA in agriculture and allied sectors stood at 4 per cent in FY2020. Share of agriculture and allied sectors in gross value added (GVA) in Indian economy at current prices stood at 17.8 per cent in FY20. Consumer spending in India will return to growth in 2021 post pandemic-led contraction, expanding by as much as 6.6 per cent (Anonymous, 2021). Total food grains production for 2020-21 is set at a record 298.30 million tonnes (MT), comprising 149.92 MT in Kharif season and 148.40 MT during Rabi season. In 2019-20, production was 291.95 MT, against the target of 291.10 MT (Anonymous, 2020b).

ABSTRACT

The tissue culture derived black pepper plants of variety Panniyur 4 were compared with conventional propagules for its vegetative growth and field performance. The in vitro derived plants recorded better rooting, survival rate and shoot growth than the conventional propagules. More than 90% of the TC derived plants recovered after primary hardening and 99% recovered after secondary hardening, while it was only 70% in conventional propagules at both the hardening stages. The secondary roots developed in TC derived plants were observed to be far more superior in number and length. The initial growth rate in terms of plant height, number and size of leaves was much better in TC derived plants. The TC derived plants developed numerous bearing shoots - laterals - in the first year of growth and started bearing in the first year itself. The performance was superior to conventional propagules in which production of laterals and bearing begins much later. Thus the performance of TC derived plants was rated as superior to conventional propagules.

Abstract

Performance records of 1085 crossbred cattle daughters of 57 sires maintained during 1974-2004 at Instructional Dairy Farm of G. B. Pant University of Agriculture & Technology, Pantnagar were used to evaluate sires for first lactation and life time performance traits. First lactation traits included were age at first calving (AFC), first lactation period (FLP),first dry period (FDP) and first calving interval (FCI) and life time traits were herd life (HL), total lactation length and life time milk yield. The data were analyzed to estimate the breeding values of sires using least squares methods (LSM), best linear unbiased prediction (BLUP) and derivative free restricted maximum likelihood (DFREML) method. The average breeding values of sires estimated by all three methods were similar and estimated for AFC, FLP, FDP and FCI as 1359.95 days, 356.56 days, 177.58 days and 534.15 days respectively and for HL, TLL and LTMY as 1641.30 days, 1320.20 days and 9110.30 kg respectively. The estimated breeding values (EBV’S) showed large genetic variation between sires for both first lactation and life time traits. The estimated breeding values (EBV’S) of sires had very high and significant product moment correlations and rank correlations among all first lactation and lifetime traits estimated by all three methods.