In 1938 and 1940, two melanistic
bobcats were trapped alive in sub-tropical
Florida. , resulting in blotchy, irregular spotting In 2003, the
dominant mode of inheritance of melanism in jaguars was confirmed by performing
phenotype-transmission analysis in a 116-individual captive
pedigree. Melanistic animals were found to carry at least one copy of a mutant
MC1R sequence
allele, bearing a 15-
base pair inframe deletion. Ten unrelated melanistic jaguars were either
homozygous or
heterozygous for this allele. A 24-base pair deletion causes the incompletely dominant allele for melanism in the jaguarundi. Sequencing of the
agouti signalling peptide in the
agouti gene coding region revealed a 2-base pair deletion in black
domestic cats. These variants were absent in melanistic individuals of
Geoffroy's cat,
oncilla,
pampas cat and
Asian golden cat, suggesting that melanism arose independently at least four times in the cat family. Melanism in leopards is inherited as a
Mendelian,
monogenic recessive trait relative to the spotted form. Pairings of black animals have a significantly smaller litter size than other possible pairings. Between January 1996 and March 2009,
Indochinese leopards were photographed at 16 sites in the
Malay Peninsula in a sampling effort of more than 1000 trap nights. Of 445 photographs of melanistic leopards, 410 were taken south of the
Kra Isthmus, where the non-melanistic morph was never photographed. These data suggest the near fixation of the dark allele in the region. The expected time to fixation of this recessive allele due to
genetic drift alone ranged from about 1,100 years to about 100,000 years. Melanism in leopards has been hypothesized to be causally associated with a selective advantage for ambush. Other theories are that genes for melanism in felines may provide resistance to viral infections, or a high-altitude adaptation, since black fur absorbs more light for warmth. ==In birds==