Although 23 different Aspergillus spp. decayed figs in California orch
ards, only A. niger occurred in more than 0.2% of the figs. The black-
spored Aspergillus isolates that caused the disease fig smut were clas
sified as A. niger var. niger, A. niger var. awamori, A. japonicus, an
d A. carbonarius. Different fungi differed in their association with A
spergillus Section Nigri (causal agents of fig smut) infections in fig
s. For example, most figs infected with Aspergillus Section Flavi (pot
ential aflatoxin producers) also had infections by Section Nigri. For
other fungi, there was either no significant relationship between fig
infections by these fungi and Section Nigri or simultaneous infections
by Section Nigri were fewer than expected. Insect damage to the fig f
ruit, predominantly by navel orangeworm (Amyelois transitella), did no
t significantly increase the colonization of figs by Aspergillus spp.
The incidences of infection by Aspergillus (Sections Nigri, Aspergillu
s, Flavi, and Circumdati) in figs differed little for different harves
ts. Figs naturally infected with A. alliaceus, A. melleus, A. ochraceu
s, and A. sclerotiorum of Aspergillus Section Circumdati contained och
ratoxin up to 9,600 ng/g, although only 40% of the figs with these fun
gi had more than a trace amount of ochratoxin. Aflatoxin contamination
in figs naturally infected with Aspergillus Section Flavi varied acco
rding to the species involved. No aflatoxins were detected in all figs
infected with A. tamarii and in most figs infected with A. flavus. Hi
gh levels of aflatoxin (>100 ng/g) were detected in 83% of the figs in
fected by A. parasiticus, but in only 32% of the figs infected by A. f
lavus. Section Flavi isolates from fig orchard soils were tested for t
heir ability to produce the mycotoxins aflatoxin and cyclopiazonic aci
d. Aspergillus parasiticus isolates always produced aflatoxin but neve
r cyclopiazonic acid; A. flavus strain S (producers of small sclerotia
) isolates always produced both aflatoxin acid cyclopiazonic acid, but
strain L (producers of large sclerotia) isolates frequently did not p
roduce aflatoxin or cyclopiazonic acid; and A. tamarii isolates never
produced aflatoxin but always produced cyclopiazonic acid. Aspergillus
flavus was recovered from the soil, at fewer than 6 CFU/g of dry soil
of every fig orchard assayed in 1992 and 1993. Although A. parasiticu
s was rarer in fig fruit than was A. flavus for each year, in orchard
soil A. parasiticus was more frequent than A. flavus. Isolates of A. f
lavus strain L were much more common in the orchard soil and fig fruit
than those of strain S. Figs in commercial orchards seem to be a favo
rable substrate for infection by and growth of Aspergillus spp.