“…elevated viability at low and high RHs, with decreased viability at medium RH), and (iv) no difference in viability as a function of RH. Because measurements of infectivity are usually collected after many minutes to hours in experiments, these results usually incorporate multiple phases of decay (§5.3), although one older study and some recent studies include sufficient temporal resolution to distinguish biphasic or triphasic decay [ 10 , 13 , 21 , 71 , 74 ]. Typically, researchers have observed increasing infectivity with increasing RH in non-enveloped viruses, for example poliovirus [ 13 , 24 , 52 ], foot-and-mouth disease virus (FMDV) [ 111 , 112 ] and rhinovirus [ 102 , 113 ], and a U-shaped trend in infectivity among enveloped viruses, for example influenza virus [ 30 , 43 , 114 ], vesicular stomatitis virus (VSV) [ 77 , 115 ] and SARS-CoV-2 [ 6 , 71 ] ( figures 1 a–c and 2 , electronic supplementary material, figures S2a–c and S3a,b).…”