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<br />002483 <br /> <br />macrophytes. In contrast, Vaseys Paradise is a fast-flowing, cool, dolomitic-type spring, with <br />abundant wetland and phreatophyte vegetation, especially native crimson monkeyflower, sedge, <br />smartweed, and poison ivy, and non-native watercress. Monkeyflower, sedge, smartweed and <br />watercress are persistent aquatic wetland or hydrophytes (Kearney and Peebles 1960), and KAS <br />is virtually restricted to those species at Vaseys Paradise (Stevens et al. 1997b, Kanab <br />Ambersnail Interagency Work Group 1997a,b). <br /> <br />Introduction of watercress at Vaseys Paradise provided KAS with an alternate host plant. KAS <br />densities are generally higher on watercress than on the native host plants during the growing <br />season (Kanab Ambersnail Interagency Work Group 1997b). Although watercress is an annual <br />species, its life cycle at Vaseys Paradise is unpredictable. In part, this irregularity is due to the <br />constant warm flows of the spring (ca. 160C), which keep the microenvironment wann enough to <br />prevent freezing during moderately cold winter months. Also, warm winters, such as 1995-1996, <br />do not freeze watercress back, while cold winters (e.g. 1990) freeze and kill the plants. Warm <br />spring flow and warm winters affect the watercress life cycle, and limit predictability of habitat <br />conditions. <br /> <br />Demographic analyses based on size class distribution indicate that KAS is essentially an annual <br />species, with much of the population maturing and reproducing in mid-summer (July and <br />August), and most snails over-wintering as small size classes (Kanab Ambersnail Interagency <br />Work Group 1 997b ). Loose, gelatinous egg masses were observed on the undersides of moist to <br />wet live stems, on the roots of water-cress, and on dead or decadent stems of crimson monkey- <br />flower in mid-summer of all years of study. No data on egg development or emergence success <br />are presently available. In warm winters, such as that of 1995-96, KAS may emerge from <br />dormancy early, and produce a double generation within one-year (Kanab Ambersnail <br />Interagency Work Group 1997a). <br /> <br />KAS at Vaseys Paradise are parasitized by the trematode flatworm, Leucochloridium <br />cvanocittae, with 1.0% to 9.5% of the mature snails expressing sporocysts in mid-summer from <br />1995 through 1997 (Stevens et al. 1997b, Kanab Ambersnail Interagency Work Group 1997 a,b). <br />Potential vertebrate predators of KAS at Vaseys Paradise include deer mice (Peromvscus crinitus <br />and.e. maniculatus), as well as rainbow trout (Oncorhvnchus mvkiss) in the stream mouth), <br />resident common raven (Corvus corax) and canyon wren (Catherpes mexicanus), summer <br />breeding Says and black phoebe (Sayornis savi and S. nigricans). and winter resident American <br />dipper (Cinclus mexicanus). <br /> <br />Natural winter mortality may reduce the KAS population by nearly an order of magnitude: the <br />lowest KAS populations observed from 1995 through 1997 occurred during emergence in <br />March, indicating winter mortality rates of 43.5% to 84.7%. March floods may result in a lower <br />total take of KAS, but the proportional take is probably approximately equivalent in any month <br />from January through July. <br /> <br />Additional factors to consider regarding differences in take between months are (l) that a BHBF <br />when watercress is abundant and in the middle of its growth phase may result in increased <br />proportional take, and (2) a BHBF from mid-May through July is likely to result in take of <br />reproductively active snails, potentially affecting annual reproductive output. Therefore, <br />although BHBF's later in the growing season may take an equal proportion of KAS, later high <br />flows may exert relatively greater impacts on KAS reproduction. <br />