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A Comparative Note on Early Sibling Aggression in Two Related Species: The Iberian and the Eurasian Lynx.

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Abstract

Early sibling fights in Eurasian and Iberian lynxes differ from other types of behavior in a lack of ritualized elements (threats) and a high motivation level. In 2005 sudden aggression, which ended up in siblicide, took place in the first Iberian lynx litter born in captivity. Fights became a problem, turning into one of the highest risks of mortality for captive born cubs. Fights started spontaneously, without any indication of previous aggression, with a very sudden and fast attack of one of the cubs in the litter. This aggression did not take place while the cubs were nursing or eating, and it did not appear to be caused by any kind of competition. Fights were not the result of an escalation of other social interactions, most times they occurred without any previous interaction (e.g., while one of the cubs was sleeping or just sitting, looking away). Litter size didn’t influence fight probability or cub mortality in any of the two species. Age at which fights occurred varied from 36-64 day in Eurasian lynx litters. In naturally raised Iberian lynxes, the appearance of sibling fights was observed during 36-63 days of life. In general, fights occurred between the 6th and 8th the Eurasian cases (18/20), but mostly during the seventh week. In Iberian lynx litters, 77% (10/13) of fights also occurred between the 6th frequent during the 6th -8th week of the cub’s life in 90% ofpostnatal weeks, being more week.Duration of after-fight aggression varied across Iberian lynx litters (median=14; min=1; max=95 days). The aggressive period in Iberian lynx lasted around 63 days (min=45; max=144). The number of attacks was higher in Eurasian than in Iberian lynx fights, but the after-fight aggressive period in Eurasian lynx was much shorter than in the Iberian lynx. Both differences could be caused by either the after-fight husbandry procedures used in the endangered species or by species-specific differences. Although fights occurred between cubs of the same and different genders, body size made a difference. Female cubs were aggressors more often than males in Eurasian lynx and the opposite was true for Iberian lynx litters. Sex ratio of aggressors did not differ from overall sex ratio in lynx litters. In general, the aggressor was larger than the attacked cub. Although several characteristics differ between Eurasian and Iberian lynx fights, this phenomenon is similar in both species, yet it differs from sibling aggression in other taxa.
Ib e r I a n l y n x
e x
s I t u
c o n s e r v a t I o n : a n In te r dI sc I pl I na ry a p p r o a c h
as t r I d va r g a s , ch r I s t I n e br e I t e n m o s e r & ur s br e I t e n m o s e r
Fu n d a c I ó n bI o d I v e r s I d a d / ca t sp e c I a l I s t gr o u p
Cats are intended to teach us that not everything in nature has
a function.
Joseph Wood Krutch
(1893-1970)
a c o m p a r a t I v e n o t e o n e a r l y s I b l I n g a g g r e s s I o n I n t w o r e l a t e d s p e c I e s : t h e Ib e r I a n a n d t h e eu r a s I a n l y n x
no t a c o m p a r a t I v a s o b r e l a a g r e s I ó n p r e c o z e n t r e h e r m a n o s d e c a m a d a e n d o s e s p e c I e s a F I n e s : e l l I n c e I b é r I c o y e l l I n c e e u r o a s t I co
an a s t a s Ia l. an t o n e v I c h , se r g e y na I d e n k o , Ju a n a be r g a r a , ev a v á z q u e z , an a st a s I o vá z q u e z ,
Ja v I e r ló p e z , an t o n I o pa r d o , an t o n I o rI v a s , Fe r n a n d o ma r t í n e z a n d as t r I d va r g a s

A comparative note on early
sibling aggression in two
related species: the Iberian and
the Eurasian lynx
Nota comparativa sobre la agresión
precoz entre hermanos de camada en dos
especies anes: el lince ibérico y el lince
euroasiático
an a s ta s I a l. an t o n e v I c h , se r g e y na I d e n k o , Ju a n a be r g a r a ,
ev a vá z q u e z , an a s t a s I o vá z q u e z , Ja v I e r ló p e z , an t o n I o pa r d o ,
an t o n I o rI v a s , Fe r n a n d o ma r t í n e z a n d as t r I d va r g a s
Re s u m e n
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Ib e r I a n l y n x
e x
s I t u
c o n s e r v a t I o n : a n In te r dI sc I pl I na ry a p p r o a c h
as t r I d va r g a s , ch r I s t I n e br e I t e n m o s e r & ur s br e I t e n m o s e r
Fu n d a c I ó n bI o d I v e r s I d a d / ca t sp e c I a l I s t gr o u p

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

   
     

 


      
       
    
          


Pa l a b R a s c l a v e

ab s t R a c t
Early sibling ghts in Eurasian and Iberian lynxes differ from other types of behavior
in a lack of ritualized elements (threats) and a high motivation level. In 2005 sudden
aggression, which ended up in siblicide, took place in the rst Iberian lynx litter born
in captivity. Fights became a problem, turning into one of the highest risks of mortality
for captive born cubs. Fights started spontaneously, without any indication of previous
aggression, with a very sudden and fast attack of one of the cubs in the litter. This
aggression did not take place while the cubs were nursing or eating, and it did not
appear to be caused by any kind of competition. Fights were not the result of an
escalation of other social interactions, most times they occurred without any previous
interaction (e.g., while one of the cubs was sleeping or just sitting, looking away). Litter
size didn’t inuence ght probability or cub mortality in any of the two species. Age at
which ghts occurred varied from 36-64 day in Eurasian lynx litters. In naturally raised
Iberian lynxes, the appearance of sibling ghts was observed during 36-63 days of
life. In general, ghts occurred between the 6th and 8th week of the cub’s life in 90% of
the Eurasian cases (18/20), but mostly during the seventh week. In Iberian lynx litters,
77% (10/13) of ghts also occurred between the 6th-8th postnatal weeks, being more
frequent during the 6th week.Duration of after-ght aggression varied across Iberian
lynx litters (median=14; min=1; max=95 days). The aggressive period in Iberian lynx
lasted around 63 days (min=45; max=144). The number of attacks was higher in
Eurasian than in Iberian lynx ghts, but the after-ght aggressive period in Eurasian
lynx was much shorter than in the Iberian lynx. Both differences could be caused by
either the after-ght husbandry procedures used in the endangered species or by
species-specic differences. Although ghts occurred between cubs of the same and
different genders, body size made a difference. Female cubs were aggressors more
often than males in Eurasian lynx and the opposite was true for Iberian lynx litters.
Sex ratio of aggressors did not differ from overall sex ratio in lynx litters. In general,
the aggressor was larger than the attacked cub. Although several characteristics differ
between Eurasian and Iberian lynx ghts, this phenomenon is similar in both species,
yet it differs from sibling aggression in other taxa.
Ke y w o R d s
Iberian lynx, Eurasian lynx, siblicide, aggressive behavior
a c o m p a r a t I v e n o t e o n e a r l y s I b l I n g a g g r e s s I o n I n t w o r e l a t e d s p e c I e s : t h e Ib e r I a n a n d t h e eu r a s I a n l y n x
no t a c o m p a r a t I v a s o b r e l a a g r e s I ó n p r e c o z e n t r e h e r m a n o s d e c a m a d a e n d o s e s p e c I e s a F I n e s : e l l I n c e I b é r I c o y e l l I n c e e u r o a s t I co
an a s t a s Ia l. an t o n e v I c h , se r g e y na I d e n k o , Ju a n a be r g a r a , ev a v á z q u e z , an a st a s I o vá z q u e z ,
Ja v I e r ló p e z , an t o n I o pa r d o , an t o n I o rI v a s , Fe r n a n d o ma r t í n e z a n d as t r I d va r g a s

A comparative note on early sibling
aggression in two related species:
the Iberian and the Eurasian lynx
an a s ta s I a l. an t o n e v I c h , se r g e y na I d e n k o , Ju a n a be r g a r a , ev a vá z q u e z , an a s t a s I o vá z q u e z , Ja v I e r ló p e z ,
an t o n I o pa r d o , an t o n I o rI v a s , Fe r n a n d o ma r t í n e z a n d as t r I d va r g a s
In t R o d u c t I o n
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
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

            

           
 
           



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Re s u l t s a n d dI s c u s s I o n
co n t e x t
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                
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ag e o f f I g h t s
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

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       < 

fI g h t f e a t u R e s
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

  
a c o m p a r a t I v e n o t e o n e a r l y s I b l I n g a g g r e s s I o n I n t w o r e l a t e d s p e c I e s : t h e Ib e r I a n a n d t h e eu r a s I a n l y n x
no t a c o m p a r a t I v a s o b r e l a a g r e s I ó n p r e c o z e n t r e h e r m a n o s d e c a m a d a e n d o s e s p e c I e s a F I n e s : e l l I n c e I b é r I c o y e l l I n c e e u r o a s t I co
an a s t a s Ia l. an t o n e v I c h , se r g e y na I d e n k o , Ju a n a be r g a r a , ev a v á z q u e z , an a st a s I o vá z q u e z ,
Ja v I e r ló p e z , an t o n I o pa r d o , an t o n I o rI v a s , Fe r n a n d o ma r t í n e z a n d as t r I d va r g a s
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5 6 7 8 9 10 11 12
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we e K s o f l I f e
n o f c u b s w h I c h f o u g h t In t h I s w e e K
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Fi g u r e 1.
Ag e o F A g g r e s s o r i n ib e r i A n
l y n x F i g h t (m o t h e r -r A i s e d A n d
h A n d -r A i s e d l i t t e r s ). in 2009,
A t t h e t i m e o F u p d A t i n g t h i s
d A t A , s e v e n n e w F i g h t s h A d t A k e n
p l A c e : t h r e e o F t h e m d u r i n g
t h e 6t h w e e k o F l i F e , o n e F i g h t
d u r i n g t h e 7t h w e e k , t w o m o r e
d u r i n g t h e 8t h p o s t n A t A l we e k ,
A n d o n e i n t h e 9t h w e e k .
Fi g u r A 1.
ed A d d e l c A c h o r r o A g r e s o r
e n c A m A d A s d e l i n c e ib é r i c o .
(cr i A d o s p o r s u s m A d r e s y
c r i A d o s A l b i b e r ó n ).
en 2009, d u r A n t e l A r e v i s i ó n
d e e s t e c A p í t u l o , h A n t e n i d o
l u g A r s i e t e p e l e A s n u e v A s :
t r e s d e e l l A s d u r A n t e l A s e x t A
s e m A n A d e v i d A , u n A d u r A n t e l A
s é p t i m A s e m A n A , d o s d u r A n t e l A
o c t A v A s e m A n A p o s t n A t A l y u n A
m á s d u r A n t e l A n o v e n A .
Fi g u r e 2.
Ag e o F F i g h t A n d d u r A t i o n o F
A g g r e s s i v e p e r i o d i n ib e r i A n
l y n x l i t t e r s , n A t u r A l A n d h A n d -
r A i s e d .
th e e n d o F t h e A g g r e s s i v e
p e r i o d h A s b e e n c A l c u l A t e d F r o m
t h e F i r s t p e A c e F u l r e u n i o n .
(or A n g e : A g g r e s s i v e p e r i o d ;
g r e e n : p e A c e F u l p e r i o d ).
Fi g u r A 2.
ed A d e n l A q u e l A p e l e A t u v o
l u g A r y d u r A c i ó n d e l p e r i o d o
A g r e s i v o e n c A m A d A s d e l i n c e
i b é r i c o , t A n t o d e c r i A n z A
n A t u r A l c o m o A r t i F i c i A l . el F i n A l
d e l p e r i o d o A g r e s i v o h A s i d o
c A l c u l A d o A p A r t i r d e l A p r i m e r A
r e u n i ó n pA c í F i c A . (nA r A n j A :
p e r i o d o A g r e s i v o ; v e r d e :
p e r i o d o p A c í F i c o ).
bR I s a y bR e z o
cy n a R a y ca t a l P a
ca s t a ñ u e l a y ca m a R I n a
da l a I y da m a
es P l I e g o y Éb a n o
en d R I n o y eo n
eu c a l I P t o y eR I z o
en e b R o y en e a
eR o s y ÉR I c a
30 50 70 90 110 130 150
da y s o f l I f e
24
21
9
7
24
14
95
1
4
Ib e r I a n l y n x
e x
s I t u
c o n s e r v a t I o n : a n In te r dI sc I pl I na ry a p p r o a c h
as t r I d va r g a s , ch r I s t I n e br e I t e n m o s e r & ur s br e I t e n m o s e r
Fu n d a c I ó n bI o d I v e r s I d a d / ca t sp e c I a l I s t gr o u p
wh o a R e t h e a g g R e s s o R s
a n d t h e v I c t I m s?

   
     
        
        
      
    

  
 


      
        
        
      
       
    
      




Re s P o n s e o f m o t h e R s t o f I g h t I n g o f f s P R I n g







co n c l u s s I o n s
    

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a c o m p a r a t I v e n o t e o n e a r l y s I b l I n g a g g r e s s I o n I n t w o r e l a t e d s p e c I e s : t h e Ib e r I a n a n d t h e eu r a s I a n l y n x
no t a c o m p a r a t I v a s o b r e l a a g r e s I ó n p r e c o z e n t r e h e r m a n o s d e c a m a d a e n d o s e s p e c I e s a F I n e s : e l l I n c e I b é r I c o y e l l I n c e e u r o a s t I co
an a s t a s Ia l. an t o n e v I c h , se r g e y na I d e n k o , Ju a n a be r g a r a , ev a v á z q u e z , an a st a s I o vá z q u e z ,
Ja v I e r ló p e z , an t o n I o pa r d o , an t o n I o rI v a s , Fe r n a n d o ma r t í n e z a n d as t r I d va r g a s
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Re f e R e n c e s
Antonevich, A.L., Naidenko, S.V., 
      

 

Drummond, H.,  

Fraser, D., Thompson, B.K., 

Hofer, H., East, M.L.,  


Naidenko, S.V., Antonevich, A.L., 







Sokolov, V.E., Naidenko, S.V., Serbenyuk, M.A., 






Vargas, A., Martínez, F., Bergara, J., Klink, L.E., Rodríguez, J.,
Rodríguez, D., 



Vargas, A., Sánchez, I., Martínez, F., Rivas, A., Godoy, J.A.,
Roldan, E., Simón, M.A., Serra, R., Pérez, M.J., Sliwa, A.,
Delibes, M., Aymerich, M., Breitenmoser, U.,  

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... Spontaneous sibling aggression is a puzzling characteristic of cub development in the lynx genus (Sokolov et al., 1994;Vargas et al., 2005;Antonevich & Naidenko, 2007;Antonevich et al., 2009). The genus Lynx includes four species: the Eurasian lynx (Lynx lynx), the Canada lynx (Lynx canadensis), the bobcat (Lynx rufus), and the most endangered felid species of the world, the Iberian lynx (Lynx pardinus) (Kitchener et al., 2017). ...
... The genus Lynx includes four species: the Eurasian lynx (Lynx lynx), the Canada lynx (Lynx canadensis), the bobcat (Lynx rufus), and the most endangered felid species of the world, the Iberian lynx (Lynx pardinus) (Kitchener et al., 2017). Sibling aggression occurs in half of the litters in Eurasian lynx (Sokolov et al., 1994) and almost all the Iberian lynx litters (Vargas et al., 2005;Antonevich et al., 2009), it leads to siblicide in some cases. Such aggression was found also in bobcats (Antonevich & Naidenko, 2013). ...
... At this period lynx females in the wild leave cubs three times a day for several hours and start to move cubs every 5-33 days using 1-4 den per month (Schmidt, 1998). Whereas in captivity females separate fi ghting cubs (Antonevich et al., 2009), in the wild females are not necessarily close to the litter and able to intervene in the fi ght, so the mortality rate can be higher. ...
... Entre la sexta y octava (figura 3.4) (Antonevich, 2009) semana de vida, los cachorros de lince ibérico desarrollan un comportamiento agresivo que provoca que se produzcan peleas continuas entre todos los integrantes de la camada. Estas agresiones han acabado con la vida de algunos cachorros, bien sea de forma directa (lesiones mortales causadas por hermanos de camada) o indirecta (causadas por la madre en su intento de separar la pelea); o con lesiones de diferente gravedad. ...
... Las agresiones se inician de forma espontánea, con un ataque repentino y rápido por parte de uno de los cachorros de la camada (Antonevich, 2009). Las agresiones no están influenciadas ni por la disponibilidad de alimento, ni por el tamaño de camada ni por el sexo de los cachorros. ...
... Las agresiones no están influenciadas ni por la disponibilidad de alimento, ni por el tamaño de camada ni por el sexo de los cachorros. Este tipo de comportamiento ha sido descrito igualmente en lince boreal y lince rojo (Antonevich, 2009(Antonevich, ,2013 Hitos en el desarrollo predatorio (Yerga, 2014) Figura 3.6. Hitos en el desarrollo predatorio en cachorros de lince ibérico. ...
Book
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Manual de trabajo del Programa de Conservación Ex-situ del Lince Ibérico que contiene las descripciones, los protocolos y las medidas para asegurar un correcto manejo de los ejemplares de lince ibérico pertenecientes al programa de cría en cautividad.
... This aggression causes injuries and rarely death of a cub. Fights start spontaneously irrespective of feeding competition, hierarchy, weaning or litter resettlement periods (Sokolov et al., 1994;Antonevich et al., 2009;). Fight results are not seen in any interactions related to feeding (Antonevich et al., in prep.), but surprisingly they affect play behavior in the litter. ...
... Both behaviors are costly, they can oppose each other because of the risks that they both impose on the animal, e.g. injuries, infection or predation (Natoli et al., 2005;Vargas et al., 2005;Antonevich & Naidenko, 2007;Kuehl et al., 2008;Antonevich et al., 2009;Lee & Moss, 2014). ...
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Social play in young mammals reflects behavioral development, play can be affected by differences in development timing and species biology. We compared social play frequency changes in three felids: Eurasian lynx (Lynx lynx), Amur subspecies of leopard cat (Far-Eastern wildcat) (Prionailurus bengalensis euptilurus) and domestic cat (Felis catus). Social play is often expected to increase social tolerance and cohesion in a litter. Socially living domestic cat had contact and non-contact social play rates at the same level as solitary lynx and leopard cat. Whereas lynx differed from the other felids in lower social play rates at the age from one to one and a half month. Two types of social play were changing differently. Non-contact play rates, attributed to predatory skills development, were synchronized among species by age of kittens. Whereas contact play changes, attributed to communication development, were sensitive to the developmental stage. Contact play intensified in lynx much later than in the other felids probably due to a later onset of weaning. The period of extraordinary low contact play rates coincided with the onset of spontaneous sibling aggression, unique for lynx. After a period of spontaneous sibling aggression contact play rates in lynx increased to the level that other felids had. Observed social play changes and differences reflect development timing and species-specific features in felids.
... Close proximity between individuals is usually related to a level of tolerance and association to another individual, and our results suggest that the cubs showed a high level of association with each other as they consistently spent high proportions of time in close proximity throughout the study period. These results highlight the difference in cub sociality in Sumatran tigers compared to other felids, such as the Iberian lynx (Lynx pardinus), where sibling fights cause high rates of first-year mortality (Antonevich and Naidenko, 2009). While the tiger cubs maintained a high level of social proximity throughout, there were times during their development, notably at five weeks old (T2), where the cubs spent slightly less time in close proximity. ...
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The modern zoo relies on the persistence of genetically and physiologically healthy populations of endangered species, which is enabled through breeding programmes globally and regionally. Many species commonly held in zoos are poorly studied in the wild, leading to a lack of in-depth knowledge surrounding breeding behaviours and subsequent parental behaviours and early life development of young. Knowledge of this information is critical to make informed management decisions which promote successful rearing of young in zoos. While the critically endangered Sumatran tiger is popular in zoos, rates of cub survival in the first 5 months are lower than 50%, highlighting the need for scientific evidence driving management decisions. This study monitors nursing and cub grooming behaviours in a first-time mother Sumatran tiger (Panthera tigris sumatrae) and her cubs throughout four stages of cub development. The social proximity of cubs and dam were recorded to describe social interactions within the group throughout cub aging. A series of Friedman tests and post-hoc tests found significant decreases in both cub grooming (χ2 (3, N = 96) = 14.20, p < 0.01) and nursing (χ2 (3, N = 96) = 25.77, p < 0.001) behaviours between the birth and weaning of the cubs, as well as within different phases of cub development between those times. Cub-to-cub proximity was maintained from birth to weaning, with cubs spending significant amounts of time in close proximity (within one adult body length) of each other (χ2 (3, N = 96) = 15.231, p = 0.001) throughout the study. The dam was found to spend significantly less time with the cubs as they reached weaning age (χ2 (3, N = 96) = 27.88, p < 0.001). These results are thought to be the first of their kind to detail timings of cub development and early life socialisation, providing evidence for timing of first food provision to young and promote the provision of space for the dam to spend time away from the cubs, while allowing the cubs to become confident, mobile, and independent.
... This in turn can have potential long-term consequences for their continued behavioral and physiological development and ultimately for fitness (Rödel and von Holst 2009;Reyes-Meza et al. 2011;Rödel and Monclús 2011;Sachser et al. 2011;Rödel et al. 2015). Also, in litters of carnivore (or semi-carnivore) species, it is generally reported that the heavier young emerge as more aggressive, dominant individuals, thus gaining access to more resources such as meat (red fox Vulpes vulpes, Henry 1985;arctic fox Vulpes lagopus, Frafjord 1993; and the Eurasian lynx Lynx lynx, Antonevich et al. 2009). Nevertheless, it has also been reported that lighter and/or socially subordinate siblings may increase their level of assertive, proactive behavior, thereby gaining greater access to resources, such as in spotted hyenas Crocuta crocuta (Benhaiem et al. 2012), meerkats Suricata suricatta (Hodge et al. 2007), and arctic foxes (Frafjord 1993). ...
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Widespread recognition of the contribution of individual differences in behavioral phenotype to evolutionary processes raises questions as to their developmental origin: when and in what contexts such differences emerge and what aspects of the developmental environment contribute to these? We studied individual differences among littermates of the domestic cat Felis silvestris catus when competing for meat at weaning, a challenging period in mammalian development. During postnatal weeks six, seven, and eight, we tested 67 weanling kittens (40 males, 27 females) from 16 litters of mixed breed cats maintained as part of a free-ranging breeding colony. Twice a week, we tested the kittens’ behavior after they were food deprived and presented together with their siblings for 2 min with a highly palatable food, a piece of raw beef. We found stable individual differences among littermates across 3 weeks of testing in latency to reach the meat, time spent eating from it, time spent monopolizing it, and number of aggressive behaviors directed toward littermates. There was no effect of sex on any of the behavioral measures. However, kittens with lower body mass at birth (and then also lower body mass at the age of testing) relative to their littermates competed more vigorously and successfully for the meat than their heavier siblings. This suggests the importance of motivational factors arising during early development in shaping individual differences in behavior such as among littermates in the present study, when competing for a biologically relevant resource. Significance statement In polytocous mammals, body mass at birth is a good predictor of growth and survival, with heavier young relative to their littermates usually obtaining a greater share of resources such as the mother’s milk. It is therefore often assumed that this advantage will translate into differences in behavior in other contexts, such that heavier littermates will gain more resources at later life stages by showing a more aggressive, “dominant” behavioral style. The findings of the present study challenge this view by demonstrating that in the domestic cat, lighter littermates were more competitive in obtaining meat at weaning. We suggest that differences in the motivational state of individuals should also be considered when accounting for the early development of individual differences in behavior, including among littermates, and may contribute to what might be broadly considered an individual’s personality or behavioral style.
... To improve elusive behaviours, lynx-human contacts were avoided and negative stimuli were sometimes conducted through direct persecutions of cubs, shouting and throwing water. Finally, to promote natural social behaviours, human handling during cub´s fighting period (Antonevich et al. 2009) was avoided and social interactions with other lynx were favoured. The training program of "Gitano", "Grazalema" and "Granadilla" was monitored through a 24hr/day video-surveillance system. ...
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With only about 350 individuals, the Iberian lynx Lynx pardinus continues to be the world’s most endangered felid. Ongoing conservation measures include both in-situ and ex-situ conservation programmes. As part of the first Iberian lynx reintroduction programme, two captive-born individuals were released in the wild in the 2010-2011 season for the first time with this species. The development of both individuals in the wild was good, as they showed natural feeding and social behaviours. Although results are preliminary, this case shows that training protocols designed for this species are working in the right direction.
... There are not differences in the time spent suckling between littermates. In the Iberian lynx, the cubs go through an aggressive period at 7 week of age [Antonevich et al., 2009]. During this aggressive period the siblings fight harshly and the first hierarchical relationships are established in the litter. ...
Article
Understanding the behavior of endangered species is crucial to improve the management tools to breed animals in captivity and, thus, to increase the success of ex situ conservation programs. In this study, we monitored suckling behavior of 26 cubs born between 2008 and 2012 at "El Acebuche" Iberian Lynx Breeding Centre. The cubs devoted 251 ± 19.7 min (mean ± SE) to lactation on the day of birth, while mothers spent 426 ± 27 min (mean ± SE) nursing their offspring. The time cubs spent suckling decreased exponentially as they grown, until they were fully weaned at 65 ± 2.6 days. The onset of weaning (first intake of solid food) occurred at 54 ± 1.35 days (mean ± SE). Thus, the strict lactation period occupied most of the overall lactation period. Both suckling and maternal behavior were affected by litter size. In twins and triplets, the competition between siblings caused a decrease in the time spent suckling, in spite of the mothers spending more time nursing their young. Finally, no significant differences were found in time spent suckling between littermates or depending on the sex of the cub. Lactation appeared to play a key role in the nutrition of the Iberian lynx and should therefore be conveniently managed in captive breeding programs of this threatened species. Zoo Biol. XX:XX-XX, 2016. © 2016 Wiley Periodicals, Inc.
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The choice of stimuli used in tests of animal behaviour can have a critical effect on the outcome. Here we report two experiments showing how different foods influence aggressive behaviour in competition tests at weaning among littermates of the domestic cat. Whereas in Experiment 1 canned food elicited almost no overt competition, a piece of raw beef rib elicited clearly aggressive behaviour among littermates. In Experiment 2 the food stimuli were chosen to differ from raw beef rib in various combinations of taste/smell, texture and monopolizability. Kittens showed different levels of aggression in response to the five stimuli tested, which suggests that the strong effect of beef rib in eliciting aggressive behaviour was due to a complex combination of features. We suggest that using stimuli approximating the evolved, functional significance to the species concerned is more likely to result in robust, biologically relevant behaviours than more artificial stimuli.
Thesis
El lince ibérico es una de las especies de mamífero más amenazada del mundo. Su cría en cautividad es una de las medidas puestas en marcha para la conservación de esta especie. Esta Tesis Doctoral tiene como objetivo describir la ontogenia física y del comportamiento de los cachorros de lince ibérico nacidos en cautividad, y conocer los factores que van a influir en su desarrollo, para mejorar el manejo de la especie en cautividad. Se realizó el seguimiento del comportamiento de los cachorros de lince ibérico nacidos en los centros de cría "El Acebuche" (Huelva, España) y "La Olivilla" (Jaén, España) entre los años 2005 y 2013, mediante un sistema de video vigilancia remota que permitía obtener los registros del comportamiento evitando las alteraciones derivadas de la presencia del observador cerca de los animales. El lince ibérico es una especie semi-altricial. Los cachorros nacieron en el interior de las parideras y no eran capaces de caminar, su desarrollo sensorial era relativamente atrasado y dependían de la madre para alimentarse. Durante el primer mes de vida, se produjo la maduración sensorial y motora, lo que permitió a los cachorros abandonar la paridera, propiciando los principales cambios en el comportamiento. El crecimiento de los cachorros se ajustó a la función de von Bertalanffy. Los machos crecieron más rápido que las hembras, de forma que eran un 8% más grandes de adultos; mientras que el método de crianza (criados con sus madres/crianza artificial) modificó la tasa de crecimiento, pero no el tamaño de adulto. La lactancia ocupó gran parte del tiempo de los cachorros durante las primeras semanas de vida, pero decreció rápidamente conforme crecieron. El destete, periodo en el que se alimentan tanto de comida sólida como de leche materna, ocurrió durante el último tercio del total del periodo lactante, por lo que el papel principal de la lactancia en el lince ibérico parece ser la nutrición de los cachorros. Una vez fuera de la paridera, la actividad diaria se incrementó hasta el tercer mes de vida, a partir del cual permaneció constante en torno al 50%. El patrón circadiano bimodal con máximos en los crepúsculos surgió en el segundo mes de vida y quedó completamente establecido a partir del tercer mes. El incremento en la actividad diaria vino acompañado de la aparición de nuevos comportamientos como el juego y la depredación. Se pudieron observar cuatro categorías de juego en los cachorros de lince ibérico. El juego social fue el primero en aparecer al mes de vida y ocupó la mayor parte del tiempo de juego de las crías. Los juegos de tipo locomotor se vieron por primera vez a los 55 días, los juegos con objetos a los 59 días y los juegos con la presa a los 61 días. El juego alcanzó su máxima prevalencia entre las semanas 11 y 14, descendiendo posteriormente, aunque sin desaparecer por completo al final del estudio. Por su parte, el proceso de aprendizaje de la caza comenzó al mes de vida, cuando la madre les llevó una presa a sus cachorros por primera vez. Las primeras etapas del aprendizaje dependieron de la iniciativa materna, que les facilitó la tarea de ingestión y captura de la presa, hasta que las crías eran capaces de cazar sin ayuda a las 15 semanas. La secuencia básica del etograma de la depredación estuvo constituida por la búsqueda, el ataque, la captura, el mordisco, el traslado de la presa y la ingesta; viéndose alterada en ocasiones por juegos o peleas. Durante el ataque, los cachorros emplearon cuatro técnicas de caza, en orden de prevalencia: acoso, rececho, acecho y persecución. El éxito total de captura fue del 53%. A partir de los resultados obtenidos se estima que la duración de las cuatro etapas del desarrollo en especies altriciales para el lince ibérico es: periodo neonatal (semanas 0 a 3); periodo de transición (semanas 4 y 5), periodo de socialización (semanas 6 a 15) y periodo juvenil (semana 16 hasta la maduración sexual).
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In the evening of 23 March 2006, Iberian lynx (Lynx pardinus) female Saliega gave birth to two healthy cubs. This is her second litter. The cubs were born in the El Acebuche Conservation Breeding Centre, where she gave last year birth to the first litter of the Critically Endangered Iberian lynx ever born in captivity (see Cat News 42).
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Abstract Sibling aggression has been studied mainly in birds, but it has also been described for a few mammalian species. In Eurasian lynx these fights occur at a specific age, mainly at the 7th week of postnatal development (63% of fights). This is not an obligate phenomenon and in a half of all litters these fights were not observed at all. Usually, fights start spontaneously, last from few minutes to a few hours and are not repeated during ontogeny in the same litter. These fights coincide with a critical period in lynx ontogeny: cubs switch to solid food, change their growth rate, intensify social relations and establish a hierarchy among littermates. Fight winners increase their growth rate during this critical period, which may provide them a better chance to survive in the wild. They also initiate more social contacts in the litter. Although there were no clear relations between probability of fights and cub’s hormonal status, the stimulation of adrenal glands with ACTH injection seemed to increase the occurrence of fights. La agresión entre hermanos ha sido estudiada principalmente en aves, pero sólo ha sido descrita en algunas especies de mamíferos. En el lince euroasiático, las peleas entre hermanos de camada son relativamente comunes y se producen a una edad determinada, principalmente en la 7ª semana de desarrollo postnatal (63%). Este fenómeno no se produce siempre, y se ha observado en aproximadamente la mitad de las camadas que han sido objeto de este estudio. Las peleas suelen iniciarse de forma espontánea, con una duración que varía desde pocos minutos hasta varias horas, y –en el caso de lince euroasiático– no se repiten durante la ontogénesis de una misma camada. Las peleas coinciden con un período crítico en el desarrollo del lince, en el que los cachorros pasan de alimentarse de leche materna a comer comida sólida. Durante este período, también se produce un cambio en la tasa de crecimiento de los cachorros; sus relaciones sociales con sus compañeros de camada se intensifican, y se establece una jerarquía entre ellos. Los ganadores de las peleas entre hermanos aumentan su tasa de crecimiento durante esta fase crítica, lo cual podría proporcionarles mayores posibilidades de supervivencia en el medio silvestre. Además, los cachorros ganadores también inician más contactos sociales en la camada. Aunque no se ha observado una relación clara entre la probabilidad de peleas y el estado hormonal de los cachorros, la estimulación de las glándulas suprarrenales mediante la inyección ACTH parece aumentar la probabilidad de las peleas. Son necesarias más investigaciones para comprender el mecanismo que desencadena el comportamiento agresivo en el lince.
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The changes in play, affiliative and aggressive relations among lynx littermates were studied for 11 kittens from 4 different litters in captivity. Sibling fights were observed in these litters at the age of 36-57 days. The fights resulted in a decrease in the frequency of playful contacts in the litters. This “fight period” coincided with the intense development of playful behavior and dietary changes. The asymmetry of playful contacts and siblings’ preferences were much clearer after the fights. These fights led to the establishment of a hierarchical dominance structure in the litters
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In the Serengeti National Park, Tanzania, large fluctuations of prey abundance alters the frequency at which spotted hyena (Crocuta crocuta) cubs are nursed and thus the total level of maternal input available to them. Maternal input is high when mothers feed on high densities of locally available migratory herbivores and low when mothers travel up to 70km to forage. Using data from 19 cub cohorts on the incidence of siblicide (from monitoring the survival of 609 cubs in twin litters) and cub growth rates (from 195 cubs in twin litters) as a measure of maternal input, we demonstrate that the incidence of siblicide increased as average cohort growth rate declined. In total, there were 37 siblicides in 384 litters (9% of litters). When both cubs were alive, total maternal input in siblicidal litters was significantly lower than in non-siblicidal litters and the mean share of the dominant sib of 64.6% was significantly higher than the mean of 52.1% for dominant sibs of non-siblicidal litters. After siblicide, growth rates of siblicide victors substantially increased, demonstrating that mothers did not reduce maternal input after litter reduction. As a result, siblicide victors achieved a long-term growth rate similar to that of singletons and thus significantly increased their expected survival. We conclude that in spotted hyenas, high maternal input in lactation has favoured the evolution of facultative siblicide in populations inhabiting areas with low or fluctuating food resources.
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Drawing on the concepts and theory of dominance in adult vertebrates, this article categorizes the relationships of dominance between infant siblings, identifies the behavioral mechanisms that give rise to those relationships, and proposes a model to explain their evolution. Dominance relationships in avian broods can be classified according to the agonistic roles of dominants and subordinates as "aggression-submission," "aggression-resistance," "aggression-aggression," "aggression-avoidance," "rotating dominance," and "flock dominance." These relationships differ mainly in the submissiveness/pugnacity of subordinates, which is pivotal, and in the specificity/generality of the learning processes that underlie them. As in the dominance hierarchies of adult vertebrates, agonistic roles are engendered and maintained by several mechanisms, including differential fighting ability, assessment, trained winning and losing (especially in altricial species), learned individual relationships (especially in precocial species), site-specific learning, and probably group-level effects. An evolutionary framework in which the species-typical dominance relationship is determined by feeding mode, confinement, cost of subordination, and capacity for individual recognition, can be extended to mammalian litters and account for the aggression-submission and aggression-resistance observed in distinct populations of spotted hyenas and the "site-specific dominance" (teat ownership) of some pigs, felids, and hyraxes. Little is known about agonism in the litters of other mammals or broods of poikilotherms, but some species of fish and crocodilians have the potential for dominance among broodmates.
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A piglet's most precious possession Is the teat that he fattens his flesh on. He fights for his teat with tenacity Against any sibling's audacity. The piglet, to arm for this mission, Is born with a warlike dentition Of eight tiny tusks, sharp as sabres, Which help in impressing the neighbors; But to render these weapons less harrowing, Most farmers remove them at farrowing. We studied pig sisters and brothers When some had their teeth, but not others. We found that when siblings aren't many, The weapons help little if any, But when there are many per litter, The teeth help their owners grow fitter. But how did selection begin To make weapons to use against kin?
Specific fights of young lynxes (Felis lynx, carnivora, Felidae)
  • V E Sokolov
  • S V Naidenko
  • M A Serbenyuk
Sokolov, V.E., Naidenko, S.V., Serbenyuk, M.A., 1994. Specific fights of young lynxes (Felis lynx, carnivora, Felidae). Zoologicheskii Zhurnal 73, 132-138