<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-22T03:18:55Z</responseDate><request verb="GetRecord" identifier="oai:repository.unam.edu.na:11070/4182" metadataPrefix="dim">https://repository.unam.edu.na/server/oai/request</request><GetRecord><record><header><identifier>oai:repository.unam.edu.na:11070/4182</identifier><datestamp>2025-11-01T22:01:10Z</datestamp><setSpec>com_11070_3405</setSpec><setSpec>com_11070_3311</setSpec><setSpec>com_11070_3304</setSpec><setSpec>col_11070_3414</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Kwembeya, E. G.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Ondigo, Lilian K.</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2025-10-30T14:10:23Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2025-10-30T14:10:23Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2021</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/11070/4182</dim:field>
   <dim:field mdschema="dc" element="description">A thesis submitted in fulfilment of the requirements for the Degree of Master of Science (By Thesis)</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">Aerial parasitic plants, commonly called mistletoes, are a polyphyletic group of 
organisms with a common evolutionary ancestor. This study was aimed at determining 
composition, spatial abundance within hosts, co-occurrence and host preference of 
mistletoes in the central highland savannas. The study site was divided into four 
sampling areas based on the presence of the distribution records of the species. Forty 
circular plots were demarcated and for every infested host plant species within these 
plots, canopy height, two diameter measurements at approximately 90", number of 
mistletoes, mistletoe species were recorded. All non-infested plant species within the 
plot were also identified and their abundances were recorded. Based on field records 
and herbarium records, four mistletoe species were identified and mapped namely; 
Oncocalyx welwitschii, Plicosepalus kalachariensis, and Tapinanthus oleifolius, 
belonging to the Family Loranthaceae and, Viscum rotundifolium which belongs to 
Family Viscaceae. A simple linear regression model established that canopy volume 
accounted for 12% of the variation in mistletoe abundance (R2 = 0.12, p &lt; 0.001). 
However, canopy diameter was a better predictor of mistletoe abundance than canopy 
volume and accounted 20% of the variation in mistletoe abundance within the host 
canopy (R2 = 0.20, p = 0.0003). Canopy volume was a poor predictor because it might 
have included branches of various sizes even those that do not support mistletoe 
establishment. Also gaps within the host canopy as well as the extent and positioning 
of branches might have led to an overestimation of the actual volume of the host 
canopy that can potentially be infested by parasites. The results further revealed a 
statistically significant relationship between mistletoe abundance and vertical canopy 
position (x2 = 67.089, df = 6, p &lt; 0.00 l) with most mistletoes occurring in the lower 
and middle third of the canopy of the host plant. The presence of V. rotundifolium and 
P. kalachariensis on the lower third of the canopy of the host plant could be explained 
by habitat preference and deposition behaviour of the Red faced mousebird ( Urocolius 
indicus). This means that the selection of this bird species for lower third of canopy 
for nesting and roosting, results in defecating of seeds more frequently on this part. On 
the contrary, the distribution ofT. oleifolius and 0. welwitschii in the middle third of 
the canopy could have been due to perch preference of the Yellow-fronted Tinker 
Barbets (Pogoniulus chrysoconus). It is possible they perch in the middle third of the 
canopy because there is a low risk of predation. Also, it could be that the branches in</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso">en</dim:field>
   <dim:field mdschema="dc" element="publisher">University of Namibia</dim:field>
   <dim:field mdschema="dc" element="subject">Aerial parasitic plants</dim:field>
   <dim:field mdschema="dc" element="subject">Polyphyletic group</dim:field>
   <dim:field mdschema="dc" element="subject">Central highland savannas</dim:field>
   <dim:field mdschema="dc" element="subject">Namibia</dim:field>
   <dim:field mdschema="dc" element="subject">University of Namibia</dim:field>
   <dim:field mdschema="dc" element="title">Composition, spatial abundance, co-occurrence and host preference of mistletoes in the Central highland savanna of Namibia</dim:field>
   <dim:field mdschema="dc" element="type">Thesis</dim:field>open.access</dim:dim></metadata></record></GetRecord></OAI-PMH>