<p><strong>Abstract.</strong> Ice nucleating particles (INPs) in the troposphere can form ice in clouds via heterogeneous ice nucleation. Yet, atmospheric number concentrations of INPs (<i>N</i><sub>INP</sub>) are not well characterized and although there is some understanding of their sources, it is still unclear to what extend different sources contribute, nor if all sources are known. In this work, we examined properties of INPs at Cape Verde from different sources, the oceanic sea surface microlayer (SML) and underlying water (ULW), the atmosphere close to both sea and cloud level as well as cloud water.</p> <p> Both enrichment and depletion of <i>N</i><sub>INP</sub> in SML compared to ULW were observed. The enrichment factor (EF) varied from roughly 0.4 to 11, and there was no clear trend in EF with temperature.</p> <p> NINP in PM<sub>10</sub> sampled at Cape Verde Atmospheric Observatory (CVAO) at any particular temperature spanned around 1 order of magnitude below &#8722;15&#8201;&#176;C, and about 2 orders of magnitude at warmer temperatures (>&#8722;12&#8201;&#176;C). <i>N</i><sub>INP</sub> in PM<sub>1</sub> were generally lower than those in PM<sub>10</sub> at CVAO. About 83&#8201;&#177;&#8201;22&#8201;%, 67&#8201;&#177;&#8201;18&#8201;% and 77&#8201;&#177;&#8201;14&#8201;% (median&#8201;&#177;&#8201;standard deviation) of INPs had a diameter >&#8201;1&#8201;&#181;m at ice activation temperatures of &#8722;12, &#8722;15, and &#8722;18&#8201;&#176;C, respectively. Among the 17 PM<sub>10</sub> samples at CVAO, three PM<sub>10</sub> filters showed elevated <i>N</i><sub>INP</sub> at warm temperatures, e.g., above 0.01&#8201;std&#8201;L<sup>&#8722;1</sup> at &#8722;10&#8201;&#176;C. However, for <i>N</i><sub>INP</sub> in PM<sub>1</sub> at CVAO, this is not the case. At these higher temperatures, often biological particles have been found to be ice active. Consequently, the difference in <i>N</i><sub>INP</sub> between PM<sub>1</sub> and PM<sub>10</sub> at CVAO, suggests that biological ice active particles were present in the super-micron size range.</p> <p> <i>N</i><sub>INP</sub> in PM<sub>10</sub> at CVAO was found to be similar to that on Monte Verde (MV, at 744&#8201;m&#8201;a.s.l.) during non-cloud events. During cloud events, most INPs on MV were activated to cloud droplets. When highly ice active particles were present in PM<sub>10</sub> filters at CVAO, they were not observed in PM<sub>10</sub> filters on MV, but in cloud water samples, instead. This is direct evidence that these INPs which are likely biological are activated to cloud droplets during cloud events.</p> <p> In general, Cape Verde was often affected by dust from the Saharan desert during our measurement. For the observed air masses, atmospheric <i>N</i><sub>INP</sub> in air fit well to the concentrations observed in cloud water. When comparing concentrations of both sea salt and INPs in both seawater and PM<sub>10</sub> filters, it can be concluded that sea spray aerosol (SSA) only contributed a minor fraction to the atmospheric <i>N</i><sub>INP</sub>. Therefore it can be said that, unless there would be a significant enrichment of <i>N</i><sub>INP</sub> during the formation of SSA particles, <i>N</i><sub>INP</sub> was mainly dominated by mineral dust at cold temperatures with few contributions from possible biological particles at warmer temperatures.</p>