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Journal ArticleDOI

Review: genetic diversity of local and exotic cattle and their crossbreeding impact on the quality of Indonesian cattle.

30 Oct 2015-Biodiversitas (Society for Indonesian Biodiversity)-Vol. 16, Iss: 2, pp 327-354
TL;DR: This crossbreeding activity was feared to change the genetic diversity of local Indonesia cattle, where the descendants could not adapt to the climatic conditions, feeds and localized diseases; and the ability of reproduction continuesto decline in generations, there was a need of regulation.
Abstract: Sutarno, Setyawan AD. 2015. Genetic diversity of local and exotic cattle and their crossbreeding impact on the quality of Indonesian cattle. Biodiversita16: 327-354.Several species of cattle had been domesticated around the world, but only two species werefarmed extensively, zebu cattle (Bos indicus) of the tropics and taurine cattle (Bos taurus) of the subtropical areas. Both of them hadhundreds variety of offspring in the worlds. The third species of cattle that most widely farmed was Bali cattle (Bos javanicus), anindigenous cattle from Indonesia that was domesticated from wild banteng (Bos javanicus javanicus). Besides Bali cattle, Indonesia hadalso some local cattle as direct descendants of or as Crossbreeds of those three cattle. These cattle had been adapted to climaticconditions, feeds and diseases in Indonesia. Local zebu cattle that relatively pure were Peranakan Ongole (PO) or Ongole breeds andSumba Ongole (SO). The main Crossbreed between zebu and Bali cattle was Madura cattle. The other well-known cattle of this wereAceh cattle, Pesisir cattle, Rancah cattle, Jabres cattle, Galekan cattle and Rambon cattle. Crossbreeds of taurine and zebu cattlegenerally produced calf that declining reproductive ability in generations. One fairly successful was Grati cattle or Holstein FreisianIndonesia (FHI) which was a crossbreed of Holstein Friesian and PO cattle. In recent decades, there were many crossbreed activitiesthrough artificial insemination between local cattle and taurine cattle to produce excellent beef cattle, mainly Simmental and Limousin.This activity was carried out widely and evenly distributed throughout Indonesia. It was conducted on all local cattle breeds and wasstrongly supported by local farmers. This crossbreeding activity was feared to change the genetic diversity of local Indonesia cattle,where the descendants could not adapt to the climatic conditions, feeds and localized diseases; and the ability of reproduction continuesto decline in generations, there fore the availability of parental cattle should be maintained continuously. This crossbreed had producedsome new breeds, among others Simpo (Simmental x PO), Limpo (Limousin x PO), Simbal (Simmental x Bali cattle), Limbal(Limousin x Bali cattle), and Madrasin or Limad (Limousin x Madura cattle). Male offsprings were sterile, while female offsprings hadlower reproductive capacity than of the parent’s. This lead to uncertainty over the guarantee of meeting the needs of protein (meat andmilk) of Indonesian in the future, thus there was a need of regulation. On the other hand, in the grasslands of North Australia, thebreeder had produced an eminent cattle breeds, namely Australian Commercial Cattle (ACC), from uncontrolled crossbreeds betweendifferent breedsof taurine and zebu cattle in the pasture, therefore this concerns ignored.

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B I O D I V E R S I T A S
ISSN: 1412-033X
Volume 16, Number 2, October 2015 E-ISSN: 2085-4722
Pages: 327-354 DOI: 10.13057/biodiv/d160230
Review:
Genetic diversity of local and exotic cattle and their crossbreeding
impact on the quality of Indonesian cattle
SUTARNO
, AHMAD DWI SETYAWAN
Department of Biology, Faculty of Mathematics and Natural Sciences, Sebelas Maret University. Jl. Ir. Sutami 36A Surakarta 57126, Central Java,
Indonesia. Tel./Fax. +62-271-663375,
email: nnsutarno@yahoo.com; volatileoils@gmail.com
Manuscript received: 3 September 2015. Revision accepted: 30 October 2015.
Abstract. Sutarno, Setyawan AD. 2015. Genetic diversity of local and exotic cattle and their crossbreeding impact on the quality of
Indonesian cattle. Biodiversita16: 327-354.Several species of cattle had been domesticated around the world, but only two species were
farmed extensively, zebu cattle (Bos indicus) of the tropics and taurine cattle (Bos taurus) of the subtropical areas. Both of them had
hundreds variety of offspring in the worlds. The third species of cattle that most widely farmed was Bali cattle (Bos javanicus), an
indigenous cattle from Indonesia that was domesticated from wild banteng (Bos javanicus javanicus). Besides Bali cattle, Indonesia had
also some local cattle as direct descendants of or as Crossbreeds of those three cattle. These cattle had been adapted to climatic
conditions, feeds and diseases in Indonesia. Local zebu cattle that relatively pure were Peranakan Ongole (PO) or Ongole breeds and
Sumba Ongole (SO). The main Crossbreed between zebu and Bali cattle was Madura cattle. The other well-known cattle of this were
Aceh cattle, Pesisir cattle, Rancah cattle, Jabres cattle, Galekan cattle and Rambon cattle. Crossbreeds of taurine and zebu cattle
generally produced calf that declining reproductive ability in generations. One fairly successful was Grati cattle or Holstein Freisian
Indonesia (FHI) which was a crossbreed of Holstein Friesian and PO cattle. In recent decades, there were many crossbreed activities
through artificial insemination between local cattle and taurine cattle to produce excellent beef cattle, mainly Simmental and Limousin.
This activity was carried out widely and evenly distributed throughout Indonesia. It was conducted on all local cattle breeds and was
strongly supported by local farmers. This crossbreeding activity was feared to change the genetic diversity of local Indonesia cattle,
where the descendants could not adapt to the climatic conditions, feeds and localized diseases; and the ability of reproduction continues
to decline in generations, there fore the availability of parental cattle should be maintained continuously. This crossbreed had produced
some new breeds, among others Simpo (Simmental x PO), Limpo (Limousin x PO), Simbal (Simmental x Bali cattle), Limbal
(Limousin x Bali cattle), and Madrasin or Limad (Limousin x Madura cattle). Male offsprings were sterile, while female offsprings had
lower reproductive capacity than of the parent’s. This lead to uncertainty over the guarantee of meeting the needs of protein (meat and
milk) of Indonesian in the future, thus there was a need of regulation. On the other hand, in the grasslands of North Australia, the
breeder had produced an eminent cattle breeds, namely Australian Commercial Cattle (ACC), from uncontrolled crossbreeds between
different breedsof taurine and zebu cattle in the pasture, therefore this concerns ignored.
Key words: Crossbreeding, exotic cattle, genetic, local cattle, quality
INTRODUCTION
Cattle raising activities have been widely practiced in
Indonesia since immemorial time. In the era of Hindu
kingdoms, cattle is commonly awarded by kings to the
Brahmin priests as an expression of gratitude, as shown in
some inscriptions, such as the inscription of Muara Kaman,
Kutai, East Kalimantan (4th century AD), the inscription of
Tugu, Jakarta (mid-5thcenturyAD), and the inscription of
Dinaya, Malang, East Java (760 AD). Cattle have long
been used as draught animals in Indonesia. A relief on the
wall of Borobudur temple, Magelang, Central Java (750
AD) showed a pair of zebu cattle (Bos indicus) is being
used for plowing, while in Sukuh, Karanganyar, Central
Java (mid-15th century AD), it is found a relief of cattle
without humps or Bali cattle (Bos javanicus) with a big
bells on the neck (Java: klonengan) as a characteristic of
draught animals (Sutarno and Setyawan 2015). In the
Islamic era, the need for cattle is increasing as the time of
Eid al-Adha celebration by slaughtering livestock.
Moreover, in some areas the fasting of Ramadan and Eid
al-Fitr were also celebrated by consuming livestock, for
example Meugang tradition of Aceh which has been traced
back to Sultan Iskandar Muda (1607-1636), thus
encouraging the development of local Aceh cattle (Yunita
2012).
Cattle are the most important livestock commodities as
a source of milk (dairy cattle), meat and leather (beef
cattle), as well as draught animals. Cattle meet most of the
world's needs for meat (50%), leather (85%) and milk
(95%) (Bappenas 2007; Umar 2009). In Indonesia, demand
for meat and dairy cattle cannot be met from domestic
stockbreeding, which can only fulfill approximately 75%
and 20% of overall need respectively, so that Indonesia
becomes a net importer of both commodities. From year to
year, dependence on imports is increasing and without
significant breakthrough, it is predicted that in the next 10
years the production of cattle in the country is only able to
meet the half of needs. In the last three years (2013, 2014,
2015), before and after Eid al-Fitr is always turmoil in the

B I O D I V E R S I T A S
16 (2): 327-354, October 2015
328
domestic market related to the soaring price of beef cattle,
due to lack of supplies. Demand for beef cattle increased
because of the population growth, improved living
standards, changing consumption patterns, and the presence
of expatriates and foreign tourists who demand beef cattle
with certain quality (DGLS 2010a; Khasrad and Ningrat
2010). The government has taken a long-term policy to
achieve self-sufficiency in beef cattle based on domestic
resources, but the effort is failed though it has been
launched three times, in 2000, 2010, and 2014. The lack of
breed quality, limited pastures and limited cattle feed are
considered as the primary reason for the cause of this
failure (DGLS 2010b; Mahbubi 2014).
This paper aims to review the genetic diversity of local
and exotic cattle in Indonesia, the crossbreeds impact and
conservation effort.
WORLDWIDE CATTLE DOMESTICATION
The domestication of wild banteng (Bos javanicus
javanicus) into Bali cattle, which continue to be the main
cattle in Indonesia until now, is a native of Indonesia's
cultural heritage that should be preserved. The yielding of
Bali cattle shows the potential of Indonesia to be an
independent and sovereign country in terms of food. Cattle
domestication process is mostly done in Europe and Asia
but yields no sustainable offspring, except for only two
species namely taurine cattle (Bos taurus) and zebu cattle
(Bos indicus). Both are descendants of wild aurochs cattle
(Bos primigenius), which is widespread in Asia, Europe,
and North Africa at the end of the last glacial period
(12,000 BP) (Felius et al. 2014). Taurine cattle
domesticated between 10,300-10,800 BP at the border
country of Turkey, Syria and Iraq (Helmer et al. 2005;
Vigne 2011; Bollongino et al. 2012), while the zebu cattle
domesticated in the Indus Valley on the desert edge of
Mehrgarh, Baluchistan, Pakistan around 8000 BP (Ajmone-
Marsan et al. 2010; Chen et al. 2010). Domestication of
species and a long history of migration, selection and
adaptation have created a wide variety of breeds
(Groeneveld et al. 2010). Based on the place of origin of
domestication, the taurine cattle (without the hump) are
sub-tropical cattle, with the main populations in Europe,
North America and Australia. While, the zebu cattle (with
the hump) are tropical cattle, with the largest population in
India, Africa and Brazil. Each species of cattle have had
hundreds of breeds, including the descent of its
crossbreeds.
Bali cattle have been domesticated from wild banteng
since c.a. 5000 BP (Payne and Hodges 1997). Bali cattle
are the most successful domestication of cattle outside
taurine and zebu cattle. When taurine and zebu cattle are
the main world livestock, Bali cattle are the main livestock
in Indonesia. However, the selection process of Bali cattle
is relatively under-developed, that it has relatively same
genetic as a wild banteng. Although, many Bali cattle is
crossed with zebu cattle and, now, with taurine cattle, but
the genetic proportion of its offspring is dominated by the
exotic cattle, so it is no longer classified as Bali cattle,
whilst the Bali cattle is relatively pure (Mohamed et al.
2009), except for Bali cattle in Malaysia which is a mixture
of zebu and banteng with relatively balanced proportion
(Nijman et al. 2003).
Domestication of the other cattle species was also
conducted in Asia (Ho et al. 2008; Achilli et al. 2009). In
Tibet, yak cattle (Bos grunniens) had been domesticated
and able to adapt to high altitudes (Qiu et al. 2012) since
c.a. 4500 BP (Payne and Hodges 1997). Gayal or mithun
cattle (Bos frontalis) had been domesticated from wild gaur
(Bos gaurus) (Uzzaman et al. 2014) on the border of
northeast India, Bangladesh and Myanmar (Mason 1988;
Payne and Hodges 1997). These species of Asia cattle
hybridize with taurine and zebu cattle that are spreading
more widely, resulting mixtures species that give a unique
contribution to the world of livestock resources (Felius et
al. 2014).
INDONESIAN LOCAL CATTLE
Indonesian local cattle has experienced a selection of
various pressures of wet tropical climate, and an adaptation
to low quality of feed, local parasitic and diseases, so it is a
new adaptive phenotypes (Sutarno 2006). Besides Bali
cattle, Indonesia has also several local cattle which are
direct descendants of the Indian zebu cattle, the result of
crossbreeding between zebu and Bali cattle, as well as
crossbreeding with taurine cattle which is introduced latter
(Martojo 2003; Johari et al. 2007). Primary crossbreeds
between zebu or taurine cattle with banteng (or Bali cattle)
produce fertile female and male sterile breeds (Lenstra and
Bradley 1999). The Indonesian local cattle are generally a
hybrid of zebu cattle with Bali cattle. Kikkawa et al. (2003)
and Mohamad et al. (2009) found mtDNA of banteng on
Indonesian zebu cattle, especially Madura cattle (56%) and
Galekan cattle (94%). While Nijman et al. (2003), based on
analysis of mtDNA and other genes, showed that Bali cattle
in Indonesia comes purely from a banteng, while Bali cattle
in Malaysia is a mixture of zebu and banteng.
Some local cattle belonging to zebu group are
Peranakan Ongole (PO) cattle in Java, Pesisir cattle in West
Sumatra, Aceh cattle in Aceh, and Sumba Ongole cattle on
the island of Sumba. India is the center of zebu cattle genes
(Nozawa 1979). Local cattle deriving from crossbreeds
between zebu and Bali cattle includes Madura cattle in
Madura and surroundings, Jabres cattle in Brebes, Rancah
cattle in Ciamis and surroundings, Rambon cattle in
Bondowoso and surroundings and the rare Galekan cattle in
Trenggalek. In Indonesia, there are also local cattle which
are considered as a crossbreed of two exotic cattle, zebu
and taurine, namely Grati cattle in Pasuruan and
surroundings, and now are more commonly known as
Holstein Friesian (FH) Indonesia, which is a cross between
FH male and PO female (Blakely and Bade 1998;
Williamson and Payne 1980; Johari et al. 2007). According
to Sutarno et al. (2015), based on studies of DNA
microsatellites, Madura cattle have most different genetic
characteristics than Bali cattle population (of Lombok and
Sumbawa) and zebu cattle population (Aceh cattle and PO

SUTARNO & SETYAWAN Genetic diversity of Indonesian cattle
329
cattle).
Bali cattle, PO cattle, and Madura cattle become a
mainstay to meet the needs of meat in Indonesia, while the
Holstein Friesian cattle become a mainstay to meet the
needs of milk (Okumura et al. 2007). Beef cattle population
in Indonesia is currently about 12.3 million (BPS 2014),
and dairy cattle is about 500,000 (DGLSAH 2014). These
cattle consist of Bali cattle (33.73%), PO cattle (23.88%),
Madura cattle (5.16%), and others (13.45%) (DGLS
2010b). The main concentration of the population of cattle
is in Java (45%), Sumatra (22%), Bali and Nusa Tenggara
(13%), Sulawesi (13%), and the rest in other islands (7%).
The population of cattle is slightly decreased after the
financial crisis at the end of 1990s, as many local cattle are
consumed to replace the imported one. The consumption
rate of local cattle exceeds the natural reproduction ability
rate; there is a decrease in the number of calf born in the
following years (Pamungkas et al. 2012).
Local cattle have proved that it can adapt to the local
environment, including feed, water availability, climate and
disease, but it generally has a lower productivity than the
exotic cattle (ILRI 1995). Adapted animals have a
production and reproduction regulating gene which are
superior to environmental stress. Conservation of local
cattle got a lot of challenges, especially since the rise of
improving the calf quality by crossbreeding using frozen
semen of exotic cattle, mainly Simmental and Limousin.
Hybrid offsprings are high favorite for breeders because it
is relatively high in daily weight gaining, although it
requires higher production costs (Sutarno 2006; Sullivan
and Diwyanto 2007). The efforts of crossbreeds are
relatively successful for the same species of cattle, such as
zebu and zebu, or taurine and taurine, but in crossbreeds of
different species, it will produce calves of sterile males and
fertile females with the ability of reproduction decreasing
from generation to generation, thus the breeders must
provide a new breeding male and female from time to time.
The crossbreeding of local cattle with exotic cattle spreads
widely without evaluation, control and ignoring the
importance of local cattle as a unique germplasm. It is
feared that it can lead to erosion of genetic resources
towards extinction. Loss of important genes in cattle that
have been locally adapted to local environmental
conditions would be difficult, or even impossible, to be
replaced. This has happened to many local cattle in India
that have become extinct before it have been identified and
utilized due to the many crossbreeds (Sodhi et al. 2006).
The weakness of cattle development in Indonesia is the
poor quality of cattle genetics, lack of superior bulls, lack
of farmers ability in dealing with cattle breeding, and
traditional method of stock raising (Atmakusuma et al.
2014). The development of local cattle is also facing
challenges due to the rise of uncontrolled crossbreeding
especially using artificial insemination methods and the
pressures of other local cattle that are more superior, for
example, the development of Pesisir cattle of West Sumatra
is suppressed by superior Bali cattle. FAO (2000) has
warned that livestock with the risk of extinction are in
developing countries due to the high market demand,
crossbreeding, breeds replacing and mechanization of
farming activities where the use of cattle as draught
animals is decreased (Figure 1).
Bali Cattle
Origin and distribution. Bali cattle (Bos javanicus)
are the result of a direct domestication of wild banteng in
Bali or Blambangan, East Java (MacHugh 1996; Verkaar et
al. 2002; Martojo, 2003, 2012; Hardjosubroto 2004). Bali
cattle spread widely throughout Indonesia, especially in
South Sulawesi, Bali, East Nusa Tenggara, West Nusa
Tenggara, Southeast Sulawesi and Lampung (Entwistle and
Lindsay 2003; Sutarno 2010). These cattle are major
genotypes in Eastern Indonesia (Pribadi et al. 2014). Bali
cattle is not much raised in Central Java and West Java
where the breeders prefers to raise goats (Capra hircus),
which are an intermediary agent of malignant catarrhal, a
deadly disease in Bali cattle calf. Bali cattle population is
about 4.1 million (DGLS 2010b). These cattle are also
found in northern Australia and Malaysia (Toelihere 2003).
In northern Australia, Bali cattle live in wild as a banteng.
They were from the 20 Bali cattle that were imported from
Bali in 1849, and now the number is around 8,000-10,000
(Bradshaw and Brook 2007). In comparison to Bali cattle,
the genetic purity of these cattle comes near to the genetic
purity of wild banteng in Java, since Bali cattle is allegedly
received genetic mixing of zebu cattle (and now taurine). In
Malaysia, Bali cattle began to be developed on a large scale
and replace the local cattle of Kedah-Kelantan that has low
productivity (Somarny et al. 2015). Bali cattle are the
ancestor of most local cattle breeds in Indonesia. In fact,
PO cattle which were considered as pure zebu cattle also
have a gene introgression of Bali cattle, as well as Pesisir
and Aceh cattle. Cattle that clearly and phenotypically pick
Bali cattle gene are Madura, Rambon, Galekan, Jabres and
Rancah cattle. But these cattle are genetically more close to
the zebu cattle (Mohamed et al. 2009).
Physical characteristics. Bali cattle has similar
physical characteristics to a wild banteng (Handiwirawan
and Subandriyo 2004), but banteng is larger and more
aggressive (Martojo 2003, 2012). The study of genetic
diversity in Bali cattle and banteng is still limited (Kikkawa
et al. 1995, 2003; Namikawa 1981; Nijman et al. 2003;
Verkaar et al. 2003). Bali cattle have a great frame and
solid muscle; adult male can weigh 600-800 kg, while the
female weigh is 500-600 kg (Martojo 2003). At the time of
calf, cattle’s body is brick red or golden red. Meanwhile,
when adult, female cattle remain red brick, while the male
cattle change to blackish at the age of 12-18 months. There
are white on all four legs, from the knee to toes, buttock is
white with clear boundaries and oval with black on tail tip
(Williamson and Payne 1980). They have no humps, a
small wattle and compact body. It has wide head, short, flat
forehead and standing ears. The female horn is short and
small, and the male horn is long and large heading to the
front upper side and taper, with a slender neck. It has deep
chest with powerful legs (Pane 1991; Susilorini 2010).
Advantages and disadvantages. Bali cattle has a very
high reproductive ability, able to give birth every year, able
to adapt to the marginal environment with dry climates,
able to digest low quality of forage for example during the

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Journal ArticleDOI
TL;DR: In Indonesia, there are several local cattle breeds of zebu that have adapted to the local condition, for example Ongole crossbred, Aceh cattle, Pesisir cattle, Sumba Ongole, and, the less commonly found, Galekan cattle of Trenggalek.
Abstract: Sutarno, Setyawan AD. 2016. The diversity of local cattle in Indonesia and the efforts to develop superior indigenous cattle breeds. Biodiversitas 16: 275-295. Cattle breeding are regarded indigenous to Indonesia. In the country, there are three types of cattle breeds: zebu (Bos indicus), Bali cattle (Bos javanicus), and taurine (Bos taurus). These breeds are farmed for their meat, milk, leather, and their power for agricultural work. Zebu was introduced by the Indians in the beginning of the first century. Bali cattle are indigenous breeds that have been domesticated from wild bantengs (Bos javanicus) in Java and Bali for hundreds of years. Several breeds of taurine were imported in early eighteenth century to be used as dairy cattle. Zebu and taurine are the major cattle breeds of the world; whereas in Indonesia, the major cattle breeds are Bali cattle, Ongole crossbred, and Madura cattle, which is a crossbred of the former two. Primary breeding between species in the genus Bos will result in sterile male and fertile female offspring. However, secondary breeding with a crossbred female will result in fertile offspring. In Indonesia, there are several local cattle breeds of zebu that have adapted to the local condition, for example Ongole crossbred, Aceh cattle, Pesisir cattle, Sumba Ongole, and, the less commonly found, Galekan cattle of Trenggalek. In addition, there are many hybrids between zebu and Bali cattle such as Madura cattle, Jabres cattle of Brebes, Rancah cattle of Ciamis, and Rambon cattle of Bondowoso, Banyuwangi, and the surrounding areas. A crossbreeding of zebu and taurine produces Grati dairy cattle. In 1970s, an Artificial Insemination program was conducted in a large scale using male cattle and semen from several breeds of zebu (Brahman, Brahman Cross) and taurine (particularly Simmental, Limousin, Holstein Friesians). The program resulted in more complex genetic mixes. Crossbreeding conducted directly in the field causes a concern since it may threaten the purity of the native species and decrease the cattle’s potential for adaptation, reproduction, and productivity. It is better to conduct crossbreeding programs privately in research centers or corporate/large farmers, of which the result can be distributed to smaller farms. “Ongolization” program that was introduced in the early twentieth century should be a lesson to learn, because it had led to the extinction of Javanese cattle, while the produced offspring, the Ongole Crossbred, are considered unsatisfactory so that they still have to be crossbred with other species of cattle, particularly taurine.

32 citations


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  • ...This manuscript is complementary to Sutarno and Setyawan (2015)....

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Journal ArticleDOI
TL;DR: The results from the CFA, PCoA, and PCA analysis in this study provide scientific evidence regarding the genetic relationship between Banteng and Bali cattle.
Abstract: Objective This research was conducted to study the genetic diversity in several Indonesian cattle breeds using microsatellite markers to classify the Indonesian cattle breeds. Methods A total of 229 DNA samples from of 10 cattle breeds were used in this study. The polymerase chain reaction process was conducted using 12 labeled primers. The size of allele was generated using the multiplex DNA fragment analysis. The POPGEN and CERVUS programs were used to obtain the observed number of alleles, effective number of alleles, observed heterozygosity value, expected heterozygosity value, allele frequency, genetic differentiation, the global heterozygote deficit among breeds, and the heterozygote deficit within the breed, gene flow, Hardy-Weinberg equilibrium, and polymorphism information content values. The MEGA program was used to generate a dendrogram that illustrates the relationship among cattle population. Bayesian clustering assignments were analyzed using STRUCTURE program. The GENETIX program was used to perform the correspondence factorial analysis (CFA). The GENALEX program was used to perform the principal coordinates analysis (PCoA) and analysis of molecular variance. The principal component analysis (PCA) was performed using adegenet package of R program. Results A total of 862 alleles were detected in this study. The INRA23 allele 205 is a specific allele candidate for the Sumba Ongole cattle, while the allele 219 is a specific allele candidate for Ongole Grade. This study revealed a very close genetic relationship between the Ongole Grade and Sumba Ongole cattle and between the Madura and Pasundan cattle. The results from the CFA, PCoA, and PCA analysis in this study provide scientific evidence regarding the genetic relationship between Banteng and Bali cattle. According to the genetic relationship, the Pesisir cattle were classified as Bos indicus cattle. Conclusion All identified alleles in this study were able to classify the cattle population into three clusters i.e. Bos taurus cluster (Simmental Purebred, Simmental Crossbred, and Holstein Friesian cattle); Bos indicus cluster (Sumba Ongole, Ongole Grade, Madura, Pasundan, and Pesisir cattle); and Bos javanicus cluster (Banteng and Bali cattle).

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  • ...The Pesisir cattle have a unique performance due to their small body (having the small est size among other Indonesian cattle breeds), and their natural habitat was only in West Sumatera, Indonesia [1]....

    [...]

  • ...Indonesia has many native breeds of cattle, including Bali cattle, Pesisir, Sumba Ongole, Madura, Aceh, Grati, Ongole Grade, Katingan, Sumbawa, Pasundan, Jabres, and Galekan (the charac­ teristics were described in Sutarno and Setyawan [1] and MARI [2])....

    [...]

  • ...This result can also be scientific evidence that the Pesisir cattle in West Sumatera, Indonesia are a type of Bos indicus cattle breeds....

    [...]

  • ...The Pesisir cattle have a unique performance due to their small body (having the small­ est size among other Indonesian cattle breeds), and their natural habitat was only in West Sumatera, Indonesia [1]....

    [...]

  • ...Keywords: Genetic Diversity, Indonesian, Cattle Breed, Microsatellite INTRODUCTION Indonesia has many native breeds of cattle, including Bali cattle, Pesisir, Sumba Ongole, Madura, Aceh, Grati, Ongole Grade, Katingan, Sumbawa, Pasundan, Jabres, and Galekan (the charac teristics were described in Sutarno and Setyawan [1] and MARI [2])....

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Journal ArticleDOI
TL;DR: In this article, the contribution of organizational learning and market orientation on business unit performance through mediation of job satisfaction is examined with Structural Equation Modeling-Partial Least Squares (SEM-PLS).
Abstract: Dairy cattle milk cooperatives in East Java has been threatened to be failure in achieving the target of Milk Self-Capacity By 2020. The reason of this failure threat is low productivity among dairy cattle milk entrepreneurs. Productivity is closely related with performance of dairy cattle milk business units, but this performance is affected by factors such as organizational learning, market orientation and job satisfaction. The objective of this research is to understand the contribution of organizational learning and market orientation on business unit performance through mediation of job satisfaction. This research is designed to use quantitative approach. The causal relationship across research variables is examined with Structural Equation Modeling-Partial Least Squares (SEM-PLS). Research population is 52 dairy cattle milk cooperatives in East Java. Sampling method is simple random sampling, and after using this sampling to populaton, it results in a sample of 46 cooperatives. Data are collected through questionnaire. Questions on questionnaire are made and processed with Software SmartPLS Version 3.27. Research has given some results: (1) Organizational Learning and Market Orientation have a positive contribution to the increase of Job Satisfaction; (2) Organizational Learning and Market Orientation do not have a positive contribution to the increase of Business Unit Performance; and (3) Job Satisfaction has a positive contribution to the increase of Business Unit Performance at dairy cattle milk cooperatives in East Java.

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Cites background from "Review: genetic diversity of local ..."

  • ...This threat of failure is caused by low dairy cattle milk production delivered by dairy cattle milk entrepreneurs (Jaenudin, Amin, Setiadi, Sumarno, & Rahayu, 2017), and it unsettles national milk stock (Nugroho, 2012; Sutarno & Setyawan, 2015)....

    [...]

Journal ArticleDOI
TL;DR: It is proved that the mineral level of Bali cattle in serum is dependent on the origin and raising habitat and Supplementation of deficient minerals in a certain area and land type is recommended to improve the performance of Blima cattle.
Abstract: . Besung INK, Watiniasih NL, Mahardika GNK, Agustina KK, Suwiti NK. 2019. Mineral levels of Bali cattle (Bos javanicus) from four different types of land in different rearing areas in Bali, Nusa Penida, and Sumbawa Islands (Indonesia). Biodiversitas 20: 2931-2936. This study aims to prove that the mineral level of Bali cattle in serum is dependent on the origin and raising habitat. Serum samples were collected from three islands in Indonesia, i.e. Bali, Nusa Penida, and Sumbawa. Samples from Bali were further classified into four different areas (i.e. agroforestry, perennial plantation, horticultural plantation, and rice field). Blood samples were collected in the jugular vein without anticoagulant. The contents of macrominerals (Ca, Mg, Na, K, P) and microminerals (Fe, Cu, Zn, Co, Mn) were measured using the flame method in atomic absorption spectrophotometer. The results showed that the level of phosphor (P) macromineral and all microminerals under study were influenced by the origin of cattle. The macrominerals are statistically varied in different cattle raising environments. The same is also valid for all microminerals, with an exception of Fe. All mineral levels under study were statistically equal in male and female Bali cattle. Phosphor macromineral and all microminerals levels were origin and environment-dependent. Supplementation of deficient minerals in a certain area and land type is recommended to improve the performance of Bali cattle.

12 citations

Journal ArticleDOI
TL;DR: Mushawwir et al. as mentioned in this paper showed that IC reduces the activity of glycogenolysis and glycolysis, but is accompanied by improvements in the biochemical conditions of liver cells.
Abstract: . Mushawwir A, Arifin J, Darwis D, Puspitasari T, Pengerteni DS, Nuryanthi N, Perman R. 2020. Liver metabolic activities of Pasundan cattle induced by irradiated chitosan. Biodiversitas 21: 5571-5578. A total of one hundred and twenty-five, 2-3 year old male Pasundan cattle were used as livestock samples during the three months of this research. They were selected from the local cattle breeding and development center in Ciamis. The animal samples were randomly allocated to 5 treatment groups. One group served as the control, or without irradiated chitosan, while the others were used as treatment in varying levels. Each treatment group involved five replicates with 25 Pasundan bulls per treatment i.e five Pasundan bulls per replication. Each group was provided with the following rations: C0 = Control group, without IC (0 ppm IC); C1 = 350 ppm Irradiated Chitosan (IC); C2 = 400 ppm IC; C3 = 450 ppm IC; and C4 = 500 ppm IC. Irradiated chitosan was obtained through the following steps: extraction, deacetylation, and irradiation of chitin using gamma rays. Five mL of blood samples were collected from each bull at the beginning of each month of this experiment, which totaled three months. The blood samples were sucked from the tail/coccygeal vein using a sterilized syringe and vacuum tube containing K3EDTA. The plasma was used to determine the concentration of parameters related to liver metabolism through an automatic biochemical analyzer Kenza 240TX model from Biolabo, using a commercial kit. Each procedure was followed based on the Biolabo kit (Franch) and Randox kit (UK). This study showed that IC reduces the activity of glycogenolysis and glycolysis, but is accompanied by improvements in the biochemical conditions of liver cells. This is a favorable condition for the metabolism of Pasundan bulls in order to enhance their growth and reproduction.

12 citations


Cites background from "Review: genetic diversity of local ..."

  • ...From the climatological aspect, they can adapt to Indonesian tropical climates (Sutarno and Setyawan 2015, 2016)....

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References
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Book
28 Jan 2010
TL;DR: Using molecular genetics in forensics and to understand species biology, the broader context: Population Viability Analysis (PVA) is examined.
Abstract: This impressive author team brings the wealth of advances in conservation genetics into the new edition of this introductory text, including new chapters on population genomics and genetic issues in introduced and invasive species. They continue the strong learning features for students - main points in the margin, chapter summaries, vital support with the mathematics, and further reading - and now guide the reader to software and databases. Many new references reflect the expansion of this field. With examples from mammals, birds, reptiles, fish, amphibians, plants and invertebrates, this is an ideal introduction to conservation genetics for a broad audience. The text tackles the quantitative aspects of conservation genetics, and has a host of pedagogy to support students learning the numerical side of the subject. Combined with being up-to-date, its user-friendly writing style and first-class illustration programme forms a robust teaching package.

3,613 citations

01 Jan 2011

3,387 citations


"Review: genetic diversity of local ..." refers background in this paper

  • ...Hybrid offsprings are high favorite for breeders because it is relatively high in daily weight gaining, although it requires higher production costs (Sutarno 2006; Sullivan and Diwyanto 2007)....

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Journal ArticleDOI
01 Mar 1990-Genetics
TL;DR: This work derives selection indices that maximize the rate of improvement in quantitative characters under different schemes of MAS combining information on molecular genetic polymorphisms (marker loci) with data on phenotypic variation among individuals (and their relatives).
Abstract: Molecular genetics can be integrated with traditional methods of artificial selection on phenotypes by applying marker-assisted selection (MAS). We derive selection indices that maximize the rate of improvement in quantitative characters under different schemes of MAS combining information on molecular genetic polymorphisms (marker loci) with data on phenotypic variation among individuals (and their relatives). We also analyze statistical limitations on the efficiency of MAS, including the detectability of associations between marker loci and quantitative trait loci, and sampling errors in estimating the weighting coefficients in the selection index. The efficiency of artificial selection can be increased substantially using MAS following hybridization of selected lines. This requires initially scoring genotypes at a few hundred molecular marker loci, as well as phenotypic traits, on a few hundred to a few thousand individuals; the number of marker loci scored can be greatly reduced in later generations. The increase in selection efficiency from the use of marker loci, and the sample sizes necessary to achieve them, depend on the genetic parameters and the selection scheme.

1,405 citations

Journal Article
TL;DR: In Introduction to Conservation Genetics, Frankham, Ballou, and Briscoe have endeavored to provide a textbook to introduce students to genetic analysis in conservation biology that maintains an impressive fluidity and is both thorough and instructive, but it has a few weaknesses worth mentioning.
Abstract: The conservation of biological diversity is a non-trivial ecological concern that has grown as human populations have expanded. In Introduction to Conservation Genetics, Frankham, Ballou, and Briscoe have endeavored to provide a textbook to introduce students to genetic analysis in conservation biology. The resulting text maintains an impressive fluidity and is both thorough and instructive, but it has a few weaknesses worth mentioning. From start to finish, Conservation Genetics maintains a coherent flow of information. Each chapter builds upon, and frequently incorporates, lessons from previous chapters while reinforcing critical concepts. These lessons are based on real data from a variety of previous studies, giving students a window into real problems that conservation biologists face. Moreover, many of these examples are accompanied by precise illustrations of the relevant organisms. They are grayscale illustrations, which limit their impact, but still enhance the reading and learning experience. The book also includes impressively instructive illustrations to diagram gene-flow schemes, pedigrees, and other complex examples. While the first few chapters focus largely on broad concepts, the authors dive into mathematical concepts such as Chi-squared analysis beginning in the fourth chapter. As the book progresses, more complex formulae are introduced, as are formulae that can be derived from previously presented equations. This progressive introduction of derived formulae helps reinforce what each variable represents, contributes to the flow of the text, and presents a sense of coherence in the mathematical tools used in the field. Examples typically include step-by-step walkthroughs of how to use the equations presented ― quite a boon for less mathematically apt students. Altogether, the vast majority of equations are utilized in such examples. While some could stand to have their derivations presented, the overall text provides excellent instruction on the use and utility of the included equations. While hardly abject disappointments, the end-of-chapter sections may be the weak point of the text. Each chapter concludes with a summary and references for further reading, both of which are perfectly useful. They also have problems that revisit key concepts and equations presented in the chapter. However, very few of the exercises engage the reader in critical thinking. Many chapters also list software tools available to researchers, but they are rarely utilized in the problems. Since computations tools can be very daunting to use, an instructor may find it beneficial to develop exercises utilizing these programs. A few omissions, such as an equations appendix, somewhat weaken the value of Conservation Genetics as a reference. With neither end-of-chapter nor end-of-book equations appendices, one must hunt through chapters to find an equation. A more minor omission is a Chi-square table. Since Chi-square analyses are a handy population genetics tool and the authors include Chi-square analyses in their text and problems, a table of Chi-square values would prove helpful. As a textbook, Introduction to Conservation Genetics is quite well written. The flow of the text keeps a reader’s attention, the material is thoroughly covered and illustrated, and the mathematical tools are particularly well explained. While there are noted weaknesses, they are not egregious, and can be easily overcome by an interested student or a creative instructor. Indeed, both should find this text a useful foundation for the learning and teaching of conservation genetics.

1,387 citations


"Review: genetic diversity of local ..." refers background in this paper

  • ...Both can be manipulated, but genetics plays a larger role because it determines the level of reproduction, productivity of meat or milk, carcass percentage, growth rate, feed efficiency, resistance to climate and disease, physical strength as draught animals, etc. (Frankham et al. 2002)....

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  • ...Conservation of genetic diversity is very important because it represents the potential evolution of a species (Frankham et al. 2002)....

    [...]