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NDF digestibility: Sheep, Horse and Black Rhinoceros

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Title: NDF digestibility: Sheep, Horse and Black Rhinoceros


1
NDF digestibility Sheep, Horse and Black
Rhinoceros
2
4 sub-species
  • South-Central (Diceros bicornis minor)
  • South-Western (Diceros bicornis bicornis)
  • East-African (Diceros bicornis michael)
  • West-African (Diceros bicornis longpipes)
  • Diceros Greek (Di two Ceros horn) and Latin
    Bicornis (Bi two Cornis horn)
  • So the southwestern black rhino is a two horn two
    horn two hornhmm

3
Physical Characteristics
  • Black rhinos attain a weight of 2,1002,900 lb
    (9501,300 kg) shoulder height of 5663 in
    (143160 cm) and head and body length of 112120
    in (286305 cm). Male and female are similar in
    size.
  • Despite name, the skin is gray to brownish gray
    in color, and devoid of hairs.
  • Horns are made of Keratin. Anterior horn is
    16.554 in (42138 cm) in length, the posterior
    one 820 in (2050 cm).
  • Have a saddle-backed appearance, rounded ears,
    and tend to hold the head high, except when
    feeding on low vegetation.

4
Behavior
  • Largely solitary, although groups of three to
    five animals may occasionally form.
  • A cow and her calf comprise the basic social
    unit, and adult males are solitary, except when
    courting a female
  • When adult males meet, a complex bull ceremony
    may take place, involving stiff-legged scraping,
    imposing postures, and short charges sometimes
    accompanied by screaming groans.
  • Females are not territorial, but males will
    tolerate submissive intruder males.

5
Behavior
  • Males mark the environment with long drag marks
    made by the legs, spray urine over bushes or
    other objects, and deposit feces on dung-heaps.
  • Females use the same dung-heaps and animals of
    both sexes scatter their droppings with
    backwardly directed kicks.

6
Distribution The Black Rhinoceros once roamed
the lower half of Africa in hundreds of
thousands. Today it survives in pockets
primarily in Zimbabwe, South Africa, Kenya,
Namibia and Tanzania.
7
Feeding Ecology and Diet
  • Live primarily on grasslands, savannahs, and
    tropical bushland habitats.
  • Predominantly low-level browsers, feeding on
    small saplings and shrubs under 5 ft (1.5 m) in
    height as well as a variety of herbs, thorny
    wood, fruit and occasionally small amounts of
    grass. They often browse in the morning and
    evening.
  • Can eat up to 220 different species of plants.
  • Can live up to 5 days without water during
    droughts.
  • Acacia spp. are especially favored, as are
    various species of Euphorbiaceae, including
    succulent forms with milky sap reputed to be
    poisonous.
  • The prehensile upper lip is used to pull twigs
    into the mouth, which are then bitten off with
    the cheek teeth. They crop branch tips up to 0.4
    in (10 mm) in thickness and 49.8 in (100250 mm)
    in length. The horns may be used to bend or break
    stems to reach higher branches. Bark may also be
    stripped from certain trees.

8
Diet Composition of Non-Captive Black
Rhinoceroses
Shrubs/Trees Herbs Grass Source
87-95 5-13 0 Joubert 1971
54-81 18-41 0 Mukinya 1977
81-94 6-19 0 Hall-martin 1982
47-93 5-51 0 Oloo 1994
93-95 3-5 1 Atkinson 1995
56-76 1-11 0-1 Pole 1995
69 31 0 Henning 2001
9
Digestion
  • Although all rhinos are hind-gut fermenters like
    rabbits and horses
  • The fact that Black Rhinos are browsers is very
    important!
  • Fundamental difference between fermentation
    characteristics of browse and grass
  • Browse has a faster fermentation rate and soon
    reaches its maximum energy release
  • Grass has a slow fermentation rate and still
    yields energy after a longer period of time

Clauss et al 2006
10
Digestion
  • White Rhino
  • Squared off upper lip used to crop grass
  • Grazes on savannah
  • Black Rhino
  • Prehensile upper lip for browsing
  • Consumes bushes and shrubs in forest

11
Comparative Anatomy Black Rhino
  • The stomach is simple, and the cecum and colon in
    the hind-gut serve as the main sites of
    fermentation
  • Short, wide colon
  • Gradual transition from colon ascendens to
    transversum

Clauss et al 2003, 2005a
12
Comparative Anatomy Horse
  • Monogastric herbivore with extensive
    post-gastric fermentation
  • Simple stomach incapable of utilization of
    forage-based (high fiber) diets
  • Abrupt shift from colon ascendens to colon
    transversum

13
Comparative Anatomy Sheep
  • Ruminant herbivore with extensive pre-gastric
    fermentation
  • Highly developed sacculated stomach capable of
    extensive and effective utilization of
    forage-based (high fiber) diets
  • Extensive fermentation before primary sites of
    digestion and absorption

14
Comparative Anatomy Capacities of GIT
Horse Sheep
450 80
8 8 17 1 2 20
27 14 41 90 6 1 3 30

BW, kg
Rumen, liters Omasum Abomasum Total stomach
Small intestine Cecum Large intestine Total GI
Black Rhino
1000
37 37
9 40 87 173
Clemens and Maloiy (1982)
15
Comparative Anatomy length of GIT (in meters)
Horse Black Rhino
S. Intestine 26.7 (76) 12.0 (66)
Caecum Colon total 1.0 (3) 7.0 (20) 0.7 (5) 4.9 (28)
DFC total Total GIT 4.5 (13) 35.0 3.7 (20) 18.5
Frewein et al
(1999) Stevens/Hume (1995)

16
Comparative Anatomy
  • There are two ways to increase passage time in a
    tubular system to shorten the length or to
    increase diameter
  • Body length does not always mean longer GIT
    (horse and tapir longer than an elephant!)
  • Browsing Rhinos have a short and wide ceacum
    (46-91 cm) compared to horses (15-18 cm)

Clauss et al 2003
17
Comparative Anatomy Average Mean Retention
Times
A longer retention time Slower passage rate
Clauss et al 2005a, Illius and Gordon 1995
18
Clinical Study Digestion Coefficients for the
Black Rhinoceros (Clauss et al 2006)
  • Objective of this study was to determine if
    horses were appropriate models for nutrient
    recommendations for the Black Rhinoceros
  • Current practice applies the equine model to
    grazing hind gut fermenters such as the white
    rhinoceros
  • It was unknown prior to this study if browsing
    behavior would reduce digestion coefficients,
    making the horse a poor model
  • Did expect that browsers would display a shorter
    ingesta retention time and lower digestion
    coefficients as compared to grazers when on
    comparable diets

19
Clinical Study Digestion Coefficients for the
Black Rhinoceros
  • Materials and Methods
  • Eight rhinos were used, selected from 3 zoos.
  • Animals were kept separate during the trial to
    allow for collection of feces and recording of
    dietary intake.
  • Protocols developed for domestic sheep (Mason and
    Frederickson 1979) were used to evaluate
    nutritional components including dry matter (DM)
    and Neutral Detergent Fiber (NDF).
  • Study compared the digestibility of rhinos to
    horses using previously published studies.
  • Additional data on browsing and grazing rhinos
    was also included from published and unpublished
    studies.

20
Clinical Study
  • Materials and Methods
  • The diets varied in total make-up but included
    some of the following
  • lucerne hay, grass hay, browse, concentrates,
    fruits and vegetables
  • Main concern was a crude fiber content that
    averaged 25 and crude protein averaging 15.

21
Clinical Study Digestion Coefficients for the
Black Rhinoceros
  • Results
  • When compared with horses from previously
    conducted studies (on similar rations), the black
    rhinoceros achieved lower digestion coefficients

22
Clauss Study Results Horses outperform Rhinos
23
Clinical Study Digestion Coefficients for the
Black Rhinoceros
  • Potential reasons
  • Comparatively shorter ingesta retention times in
    the black rhino (Clauss et al 2005b)
  • Among wild ruminant species, it has been
    demonstrated that browsing species achieve lower
    coefficients than grazing species (Iason and Van
    Weiren 1999)
  • Hackenberger (1987) demonstrated that the African
    elephant which is thought to be adapted to a diet
    with more browse material than its Asian
    counterpart also displays shorter retention times
    and decreased digestion of grass hay

24
Dont take our word for itBrowsers vs. Grazers
25
Why?
  • The digestive strategy of long retention times to
    increase digestion coefficients is an
    evolutionary adaptation one would expect in
    grazing species- whether hind gut or foregut
    fermenters
  • Grass has a slow fermentative rate and still
    gives energy even after a long period of time

26
The why, continued
  • Shorter retention times are expected in browsing
    species
  • browse has a faster fermentation rate and soon
    reaches its maximum energy release
  • So if you gave a browsing rhino Alfalfa, youd
    expect that it wouldnt reach its full energy
    potential because its not fermented long enough.
    Youd also expect that hed want to eat a lot
    more.

27
So, the Black Rhino comes to NUT 115 and eats
alfalfa pellets
  • Real and Expected Digestibility order
  • Sheep 63.7 DM/43.9 NDF
  • Horse 58.6 DM/27.2 NDF
  • Rhino 53 DM/26 NDF

28
FYI More on the Vit E Question
  • Problem Rhinoceros accumulate body stores of
    iron over their lifetime that may be associated
    with numerous maladies ie captive black
    rhinoceroses have a history of disease and death
    characterized by hemolytic anemia and
    mucocutaneous ulceration
  • Current trends Iron and copper supplements have
    been routinely given to captive rhinos. In the
    absence of species specific data, nutrient levels
    are based on work performed with domestic
    livestock.
  • Potential Causes Many nutrients listed as
    possible causes in the syndromes may be linked in
    some way to each other
  • Specific nutrients of concern ferric iron
    antagonist to vitamin E, interactions between
    absorption of dietary iron and vitamin E, and
    linkages between copper and iron
    absorption/functioning.
  • Wild Rhino Diet Natural browse of black
    rhinoceros contains secondary plant compounds
    including tannins that may decrease mineral
    absorption. It is possible that these chemicals
    may bind excess dietary iron in the natural diet.
    Commercial hays contain tannins, but at lower
    levels and are fed to captive rhinos (budget,
    absence of data, etc)
  • Diets without tannins are hypothesized to cause
    increased iron absorption and an insufficient
    antioxidant status, and therefore to contribute
    to disease symptoms observed in captive black
    rhinos
  • Current study at the Brookfield Zoo (Illinois)
    "Dietary Iron Absorption and the Role of Tannins
    in Eastern (Diceros bicornis michaeli) and
    Southern Black Rhino (Diceros bicornis minor), a
    Comparison"
  • Website http//www.sosrhino.org/research/black_rh
    ino_nutrition2.php last acessed 3/13/06

29
References
  • CLAUSS M CASTELL J.C KIENZLE E DIERENFELD E.S
    FLACH E.J BEHLERT O ORTMAN S STREICH W.J
    HUMMEL J HATT J.M (2006) Digestion coefficients
    achieved by the black rhinoceros (diceros
    bicornis), a large browsing hind gut fermenter.
    Journal of Animal Physiology and Animal Nutrition
    90 325-334.
  • OFTEDAHL, O., BAER, D.J., AND ALLEN, M.E. (1996).
    The feeding and nutrition of herbivores. In
    Kleiman, D.G., Allen, M., Thompson, K.V., and
    Lumpkin, S. (eds), Wild Mammals in Captivity
    Principles and Techniques. University of Chicago
    Press, Chicago, IL. 129-138.
  • GHEBREMESKEL, K.WILLIAMS, G. BRETT, R.A.
    BUREK, R. HARBIGE, L.S (1991) Nutrient
    composition of plants most favoured by black
    rhinoceros (Diceros bicornis) in the wild.
    Comparative Physiology 98 529534.
  • OWEN-SMITH, N. (1975) The social ethology of the
    white rhinoceros (Ceratotherium simum). Z.
    Tierpsychology 38 337.
  •  
  • HOFMANN, R.R. (1989) Evolutionary steps of
    ecophysiological adaptation and diversification
    of ruminants A comparative view of their
    digestive system. Oecologia 78443-457.
  • CLAUSS M FROESCHLE T CASTELL J HUMMEL J HATT
    J-M ORTMANN S STREICH W.J (2005) Fluid particle
    retention times in the black rhinoceros. Acta
    Theriologica 50 367-376.
  • CLAUSS M FREY R KIEFER B LECHNER-DOLL M
    LOEHLEIN W POLSTER C ROSSNER G.E STREICH W.J
    (2003) The maximum attainable body size of
    herbivorous mammals constraints on forgut, and
    adaptations of hindgut fermenters. Oecologia 136
    14-27
  • VAN SOEST, P (1994) Nutritional ecology of the
    ruminant, 2nd ed. Cornell University Press,
    Ithaca, NY
  • CLAUSS M POLSTER C KIENZLE E WIESNER H
    BAUMGARTNER K VON HOUWALD F ORTMANN S STREICH
    W.J DIERENFELD E.S (2005) Studies on digestive
    physiology and feed digestibilities in captive
    Indian rhinoceros (Rhinoceros unicornis) Journal
    of Animal Physiology and Animal Nutrition 89
    229237.
  • HACKENBERGER M.K., 1987 Diet digestibilities and
    ingesta transmit times of captive Asian and
    African elephants. MS thesis, University of
    Guelph, Canada, pp. 1-115.
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