Antibody (Ab)-dependent and -independent activation of the duck complement (C9 ) system were studied. Ab-independent C9 activity exhibited characteristics similar to those of the mammalian alternative C9 pathway (ACP), including the selective lysis of rabbit erythrocytes (RRBC), a requirement for Mg 2 1 , but not Ca 2 1 , depletion of activity by zymosan, and lack of sensitivity to the mammalian C1 inhibitor carrageenan. Measurement of C9 activity using antisera against sheep erythrocytes (SRBC) revealed that duck Abs activate C9 by a pathway resembling the mammalian classical pathway (CCP) requiring both Ca 2 1 and Mg 2 1 . Ab-dependent and -independent activities were further distinguishable by their kinetics of lysis and sensitivities to heat. Duck Abs were also found to activate C9 in normal and carrageenantreated serum by a mechanism that requires only Mg 2 1 , and thus resembles the ACP. However, this Ab-dependent ACP-like activity exhibits patterns of ionic strength dependence and ontogeny which are clearly different from those of the conventional ACP and CCP. These ® ndings indicate that duck C9 can be activated by three mechanisms: Ab-mediated activation of the CCP, and Ab-mediated and Ab-independent activation of the ACP. Duck Ab responses to SRBC and RRBC were followed by direct agglutination, antiglobulin agglutination, and activation of the CCP and ACP. While the C9 -activating abilities of duck anti-SRBC Abs persisted through a 3-month programme of inoculation, the anti-RRBC response lost its ability to activate C9 after 2 weeks.