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Journal articles on the topic 'Vascular plants in Zambia'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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1

PHIRI, P. S. M., and D. M. MOORE. "A history of botanical collections in the Luangwa Valley, Zambia." Archives of Natural History 25, no. 2 (June 1998): 283–91. http://dx.doi.org/10.3366/anh.1998.25.2.283.

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Central Africa remained botanically unknown to the outside world up to the end of the eighteenth century. This paper provides a historical account of plant explorations in the Luangwa Valley. The first plant specimens were collected in 1897 and the last serious botanical explorations were made in 1993. During this period there have been 58 plant collectors in the Luangwa Valley with peak activity recorded in the 1960s. In 1989 1,348 species of vascular plants were described in the Luangwa Valley. More botanical collecting is needed with a view to finding new plant taxa, and also to provide a satisfactory basis for applied disciplines such as ecology, phytogeography, conservation and environmental impact assessment.

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2

Subrahmanyam, P. "New Hosts of the Parasitic Flowering Plant, Alectra vogelii, in Malawi." Plant Disease 85, no. 4 (April 2001): 442. http://dx.doi.org/10.1094/pdis.2001.85.4.442c.

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Alectra vogelii Benth. (Family: Scrophulariaceae) is a vascular hemiparasite of various leguminous crops in Africa, including peanut (Arachis hypogaea), bambara groundnut (Vigna subterranea), cowpea (Vigna unguiculata), common bean (Phaseolus vulgaris), soybean (Glycine max), and mung bean (Vigna radiata) (1). It is a common parasite of peanut in Angola, Burkina Faso, Malawi, Mozambique, Nigeria, Swaziland, Zambia, and Zimbabwe (2). During April and May 2000, A. vogelii was observed parasitizing several wild Arachis species in a field at the Chitedze Agricultural Research Station near Lilongwe, Malawi. These species were part of a germ plasm enhancement program that included A. appressipila (ICRISAT Groundnut Accession number [ICG] 8127), A. batizocoi (ICG 8124), A. benensis (ICG 13215), A. cardenasii (ICG 13164 and 13166), A. correntina (ICG 8918), A. duranensis (ICG 13200), A. helodes (ICG 8955 and 14917), A. hoehnei (ICG 13228), A. magna (ICG 8960), A. pintoi (ICG 13222 and 14914), A. stenosperma (ICG 13172 and 13223), and A. valida (ICG 13230). In addition, A. vogelii was observed on four unidentified Arachis species (ICG 13231, 14875, 14888, and 14907). Parasitized plants were less vigorous and connections between A. vogelii and host plants could be observed by carefully removing the soil in the root zone. Mature A. vogelii plants were 0.3 to 0.5 m and had multiple stems branching at the base. Subsoil plant parts were a deep orange color. Flowers were prominent lemon yellow with horseshoe-shaped stigmata and leaves were light green. This is the first report of A. vogelii parasitizing wild Arachis species. References: (1) C. Parker. Crop Prot. 10:6–22, 1991. (2) P. Subrahmanyam. 1997. Parasitic flowering plants. Pages 70–71 in: Compendium of Peanut Diseases, 2nd Ed. N. Kokalis-Burelle, D. M. Porter, R. Rodriguez-Kabana, D. H. Smith, and P. Subrahmanyam, eds. American Phytopathological Society, St. Paul, MN.

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3

Doyle, James A. "PHYLOGENY OF VASCULAR PLANTS." Annual Review of Ecology and Systematics 29, no. 1 (November 1998): 567–99. http://dx.doi.org/10.1146/annurev.ecolsys.29.1.567.

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4

Lepp, Nicholas W. "Vascular Transport in Plants." Journal of Environmental Quality 35, no. 2 (March 2006): 688. http://dx.doi.org/10.2134/jeq2005.0019br.

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5

Ding, Yiliang, and Chun Kit Kwok. "Emergence of vascular plants." Nature Plants 4, no. 6 (May 28, 2018): 325–26. http://dx.doi.org/10.1038/s41477-018-0159-0.

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6

Sorrie, Bruce A. "Alien vascular plants in Massachusetts." Rhodora 107, no. 931 (October 2005): 284–329. http://dx.doi.org/10.3119/0035-4902(2005)107[0284:avpim]2.0.co;2.

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7

IWATSUKI, Kunio. "Endangered vascular plants in Japan." Proceedings of the Japan Academy, Series B 84, no. 8 (2008): 275–86. http://dx.doi.org/10.2183/pjab.84.275.

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8

Crandall-Stotler, Barbara, and Mohammad Iqbal. "Growth Patterns of Vascular Plants." Bryologist 101, no. 2 (1998): 353. http://dx.doi.org/10.2307/3244215.

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9

Lee, Yong No. "Outline of Korean vascular plants." Korean Journal of Plant Taxonomy 28, no. 1 (March 31, 1998): 111–16. http://dx.doi.org/10.11110/kjpt.1998.28.1.111.

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10

EDWARDS, DIANNE. "Preservation in early vascular plants." Geology Today 2, no. 6 (November 1986): 176–81. http://dx.doi.org/10.1111/j.1365-2451.1986.tb00202.x.

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11

Walles, Björn. "Growth patterns in vascular plants." Nordic Journal of Botany 15, no. 6 (December 1995): 582. http://dx.doi.org/10.1111/j.1756-1051.1995.tb02125.x.

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12

Alberdi, Miren, León A. Bravo, Ana Gutiérrez, Manuel Gidekel, and Luis J. Corcuera. "Ecophysiology of Antarctic vascular plants." Physiologia Plantarum 115, no. 4 (July 11, 2002): 479–86. http://dx.doi.org/10.1034/j.1399-3054.2002.1150401.x.

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13

Kenrick, P. "The relationships of vascular plants." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 355, no. 1398 (June 29, 2000): 847–55. http://dx.doi.org/10.1098/rstb.2000.0619.

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Recent phylogenetic research indicates that vascular plants evolved from bryophyte–like ancestors and that this involved extensive modifications to the life cycle. These conclusions are supported by a range of systematic data, including gene sequences, as well as evidence from comparative morphology and the fossil record. Within vascular plants, there is compelling evidence for two major clades, which have been termed lycophytes (clubmosses) and euphyllophytes (seed plants, ferns, horsetails). The implications of recent phylogenetic work are discussed with reference to life cycle evolution and the interpretation of stratigraphic inconsistencies in the early fossil record of land plants. Life cycles are shown to have passed through an isomorphic phase in the early stages of vascular plant evolution. Thus, the gametophyte generation of all living vascular plants is the product of massive morphological reduction. Phylogenetic research corroborates earlier suggestions of a major representational bias in the early fossil record. Megafossils document a sequence of appearance of groups that is at odds with that predicted by cladogram topology. It is argued here that the pattern of appearance and diversification of plant megafossils owes more to changing geological conditions than to rapid biological diversification.

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14

FAHN, ABRAHAM. "Secretory tissues in vascular plants." New Phytologist 108, no. 3 (March 1988): 229–57. http://dx.doi.org/10.1111/j.1469-8137.1988.tb04159.x.

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15

Duckett, Jeffrey G., and Silvia Pressel. "Of mosses and vascular plants." Nature Plants 6, no. 3 (March 2020): 184–85. http://dx.doi.org/10.1038/s41477-020-0619-1.

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16

Black, M. "Storage carbohydrates in vascular plants." FEBS Letters 206, no. 1 (September 29, 1986): 176–77. http://dx.doi.org/10.1016/0014-5793(86)81373-4.

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17

Ticha, I. "Growth patterns in vascular plants." Biologia plantarum 37, no. 2 (June 1, 1995): 250. http://dx.doi.org/10.1007/bf02913221.

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18

Verhey, Steven D., and Terri L. Lomax. "Signal transduction in vascular plants." Journal of Plant Growth Regulation 12, no. 4 (October 1993): 179–95. http://dx.doi.org/10.1007/bf00213036.

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19

Knapp, Wesley M., and Robert F. C. Naczi. "Vascular Plants of Maryland, USA:." Smithsonian Contributions to Botany, no. 113 (May 17, 2021): iv—151. http://dx.doi.org/10.5479/si.14605674.v1.

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This checklist provides the first complete, vouchered account of Maryland’s vascular flora. In total, we discuss 3,525 taxa and document 2,918 established taxa for the state of Maryland, 71.8% of which are native and 28.2% of which are introduced. Of the native species, 737 (25.3%) are tracked by the Maryland Natural Heritage Program as of conservation concern. We exclude 324 taxa reported from Maryland by previous authors and provide justifications for these exclusions.

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20

Keener, Carl S., Ernest M. Gifford, and Adriance S. Foster. "Morphology and Evolution of Vascular Plants." Systematic Botany 15, no. 2 (April 1990): 348. http://dx.doi.org/10.2307/2419189.

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21

Schmid, Rudolf, and Ernest M. Gifford. "Morphology and Evolution of Vascular Plants." Taxon 38, no. 4 (November 1989): 613. http://dx.doi.org/10.2307/1222641.

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22

Ferguson, David K., and Wentsai Wang. "Vascular Plants of the Hengduan Mountains." Taxon 46, no. 2 (May 1997): 386. http://dx.doi.org/10.2307/1224129.

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23

De Groot, Sarah. "Vascular Plants of the Whipple Mountains." Aliso 24, no. 1 (2007): 63–96. http://dx.doi.org/10.5642/aliso.20072401.06.

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24

Atsatt, Peter R. "Are Vascular Plants "Inside-Out" Lichens?" Ecology 69, no. 1 (February 1988): 17–23. http://dx.doi.org/10.2307/1943156.

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25

Barclay, Colville. "Crete: Checklist of the Vascular Plants." Englera, no. 6 (1986): I. http://dx.doi.org/10.2307/3776733.

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26

Major, Jack. "Distribution of Vascular Plants in Utah." Ecology 71, no. 2 (April 1990): 830–31. http://dx.doi.org/10.2307/1940338.

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27

Houle, Gilles. "Vascular Plants of Arabia Mountain, Georgia." Bulletin of the Torrey Botanical Club 114, no. 4 (October 1987): 412. http://dx.doi.org/10.2307/2995997.

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28

König, Christian, Patrick Weigelt, and Holger Kreft. "Dissecting global turnover in vascular plants." Global Ecology and Biogeography 26, no. 2 (November 13, 2016): 228–42. http://dx.doi.org/10.1111/geb.12536.

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29

Stroock, Abraham D., Vinay V. Pagay, Maciej A. Zwieniecki, and N. Michele Holbrook. "The Physicochemical Hydrodynamics of Vascular Plants." Annual Review of Fluid Mechanics 46, no. 1 (January 3, 2014): 615–42. http://dx.doi.org/10.1146/annurev-fluid-010313-141411.

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30

Larsen, Kai. "Vascular plants synopsis of Vietnamese flora." Nordic Journal of Botany 16, no. 5 (December 1996): 504. http://dx.doi.org/10.1111/j.1756-1051.1996.tb00264.x.

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31

Aedo, C., L. Medina, P. Barberá, and M. Fernández-Albert. "Extinctions of vascular plants in Spain." Nordic Journal of Botany 33, no. 1 (September 5, 2014): 83–100. http://dx.doi.org/10.1111/njb.00575.

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32

Chawla, Amit, Om Parkash, Varun Sharma, S. Rajkumar, Brij Lal, Gopichand, R. D. Singh, and A. K. Thukral. "Vascular plants, Kinnaur, Himachal Pradesh, India." Check List 8, no. 3 (June 1, 2012): 321. http://dx.doi.org/10.15560/8.3.321.

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In the present study, we provide a checklist of the vascular plants of Kinnaur district situated in the Himachal Pradesh state of India in the western Himalaya. This checklist includes 893 taxa (viz., species, subspecies and varieties) belonging to 881 species of angiosperms and gymnosperms distributed among 102 families and 433 genera, and 30 species of pteridophytes. Information about the growth habit, threat and endemicity status is also provided. Our results show that family Compositae is by far the most species rich family with 122 species, followed by Poaceae (69), Rosaceae (58), Leguminosae (49) and Lamiaceae (38). Among the genera, Artemisia is the most diverse genus with 19 species, followed by Potentilla (14), Saussurea (13), Polygonum (11), Astragalus (10), Lonicera (10) and Nepeta (10). Similar to other regions in the western Himalayan range, family-to-genera ratio was 1:4.25 and the genera-to-species ratio was 1:2.04. Out of 893 taxa, our checklist includes 606 herb species, 63 trees, 108 shrubs, 28 climbers, 67 graminoids and 21 sedges and rushes. Of all the species recorded, 108 (12.2%) are endemic to western Himalaya and 27 (3%) are placed under IUCN threatened categories. The present checklist on the flora of Kinnaur provides an important baseline data for further quantitative studies on the characteristics of plant communities in this region and will help in the identification of priority conservation areas.

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33

Einarsson, Eythór, and Eythor Einarsson. "Vascular Plants of the Thingvallavatn Area." Oikos 64, no. 1/2 (May 1992): 117. http://dx.doi.org/10.2307/3545047.

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34

Bowles, David E. "Vascular plants of Mammoth Spring, Arkansas1." Journal of the Torrey Botanical Society 147, no. 1 (February 17, 2020): 87. http://dx.doi.org/10.3159/torrey-d-19-00019.1.

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35

Buck, Paul. "Vascular Plants of the Wichita Mountains." Oklahoma Native Plant Record 2, no. 1 (December 1, 2002): 4–21. http://dx.doi.org/10.22488/okstate.17.100011.

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36

Wallis, Charles. "Vascular Plants of the Oklahoma Ozarks." Oklahoma Native Plant Record 7, no. 1 (December 1, 2007): 4–20. http://dx.doi.org/10.22488/okstate.17.100051.

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37

Elzenga, J. Theo M., Christopher P. Keller, and Elizabeth Van Volkenburgh. "Patch Clamping Protoplasts from Vascular Plants." Plant Physiology 97, no. 4 (December 1, 1991): 1573–75. http://dx.doi.org/10.1104/pp.97.4.1573.

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38

Abdel‐Shafy, Hussein I., Werner Hegemann, and Andrea Teiner. "Accumulation of Metals by Vascular Plants." Environmental Management and Health 5, no. 2 (June 1994): 21–24. http://dx.doi.org/10.1108/09566169410057137.

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39

BARINA, ZOLTÁN, GABRIELLA SOMOGYI, DÁNIEL PIFKÓ, and MARASH RAKAJ. "Checklist of vascular plants of Albania." Phytotaxa 378, no. 1 (November 26, 2018): 1. http://dx.doi.org/10.11646/phytotaxa.378.1.1.

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This work includes all names of higher plants reported or collected in the present territory of Albania. The records are critically evaluated; the origin of them was tracked down and possible vouchers were searched for, revised and evaluated. Altogether, 6,419 basionyms were identified with 5,480 recently accepted taxa and their nativity status were examined.

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40

Sugden, Andrew M. "The vascular plants of the Americas." Science 358, no. 6370 (December 21, 2017): 1551.5–1552. http://dx.doi.org/10.1126/science.358.6370.1551-e.

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41

Nishihiro, Jun, Munemitsu Akasaka, Mifuyu Ogawa, and Noriko Takamura. "Aquatic vascular plants in Japanese lakes." Ecological Research 29, no. 3 (March 16, 2014): 369. http://dx.doi.org/10.1007/s11284-014-1139-0.

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42

Jin, Zhenfu, Shunliu Shao, Kyoko S. Katsumata, and Kenji Iiyama. "Lignin characteristics of peculiar vascular plants." Journal of Wood Science 53, no. 6 (December 2007): 520–23. http://dx.doi.org/10.1007/s10086-007-0891-y.

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43

Dentant, Cédric. "The highest vascular plants on Earth." Alpine Botany 128, no. 2 (July 30, 2018): 97–106. http://dx.doi.org/10.1007/s00035-018-0208-3.

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44

Schmid, V. H. R. "Light-harvesting complexes of vascular plants." Cellular and Molecular Life Sciences 65, no. 22 (September 15, 2008): 3619–39. http://dx.doi.org/10.1007/s00018-008-8333-6.

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45

Sheremetova, Svetlana, Irina Khrustaleva, and Peter Stieglbauer. "Biodiversity of vascular plants of Kuzbass." BIO Web of Conferences 31 (2021): 00023. http://dx.doi.org/10.1051/bioconf/20213100023.

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The latest vascular plants biodiversity data of Kuzbass region is presented. The species that should be excluded from the Kemerovo region flora list are reported. The species that require further research for making an exclusion from Kuzbass vascular plants species list are mentioned. Additionally, rare species that can already be attributed to disappeared ones from the territory of the region are noted. It is established that there are 1728 species of vascular plants at the present time on the territory of Kuzbass.

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46

Kapooria, R. G., J. Ndunguru, and G. R. G. Clover. "First Reports of Soilborne wheat mosaic virus and Wheat spindle streak mosaic virus in Africa." Plant Disease 84, no. 8 (August 2000): 921. http://dx.doi.org/10.1094/pdis.2000.84.8.921c.

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During 1997 and 1998, virus symptoms similar to those of Soilborne wheat mosaic virus (SBWMV) and Wheat spindle streak mosaic virus (WSSMV) were observed on nine wheat cultivars (Triticum aestivum cvs. Deka, Gamtoos, Lorie II, MM2, Nata, Nkwazi, P7, Scepter, and Scan) in the Central, Copper-Belt, Lusaka, and Southern provinces of Zambia. Symptoms were observed between June and August on wheat, which in Zambia is an irrigated crop grown during the cooler months (May to August). In fields suspected to be infected with SBWMV, irregularly distributed, circular patches of severely stunted sparse plants were observed. Because of these symptoms, the syndrome is described in Zambia as the “crater disease.” Infection was more common on light to medium sandy-loam clay soils, and affected patches were particularly common along the field edges and in poorly drained areas. Such waterlogged conditions are conducive to the multiplication and spread of Polymyxa graminis, the protist vector of SBWMV (1). Affected plants initially showed chlorotic streaks on all leaves, which became uniformly yellow and eventually necrotic. The roots of these plants were slightly swollen and enlarged and are likened to “Rastafarian pleats” locally. In fields suspected to be infected with WSSMV, symptomatic plants were observed in the border rows of affected fields. Chlorotic streaks and mosaics were observed on the leaves of affected plants, and the tips of these leaves were also frequently twisted. Using double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA), SBWMV and WSSMV were positively identified in symptomatic plants. In total, 81 plants from the four provinces were tested, and 72 and 37% were infected with SBWMV and WSSMV, respectively. Identification was confirmed by DAS-ELISA using antisera from W. Huth (BBA-Braunschweig, Germany) and C. Rubies-Autonell (Bologna University, Italy) for SBWMV and using antisera from W. Huth (BBA-Braunschweig, Germany) and G. Bergstrom (Cornell University, New York) for WSSMV. Further confirmation of the identity of the two viruses was provided by the reaction of 12 indicator species (Chenopodium amaranticolor, C. quinoa, C. hybridum, Digitaria milanjiana, Eleusine indica, Oryza sativa (cv. IITA 212), Panicum maximum, Rottboellia cochinchinensis, Setaria verticillata, Sorghum bicolor(cv. Sima), S. halepense, and Triticum aestivum (cvs. Lucal, Kwale, Lorie II, Nkanga, 128, and GV 4–12) in mechanical transmission studies using infected leaf sap. This is the first report of SBWMV and WSSMV not only in Zambia but also Africa. The area of wheat grown in Zambia has risen in the past several years to approximately 18,000 ha per annum. However, annual wheat yield (60,000 tons) has not risen to match this increase. The effect of SBWMV and WSSMV on yield in Zambia has not yet been measured, but both viruses cause serious losses in other countries (1–3) and the severity of the symptoms suggests that significant yield reductions are likely. Furthermore, no Zambian wheat cultivars are known to be resistant to either virus. Generally, wheat production fails to meet demand in the country and therefore further yield losses due to virus infection could be disastrous. References: (1) M. K. Brakke. CMI/AAB Desc. of Plant Viruses 77, 1971. (2) J. T. Slykhuis. Phytopathology 60:319, 1970. (3) V. Vallega and C. Rubies-Autonell. Plant Dis. 69:64, 1985.

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47

Kachenga, Lupupa, Harry Nixon Chabwela, and Kasuka Mwauluka. "Phytoremediation Potential of Indigenous Plants Growing at Nchanga Mine in Chingola, Zambia." Open Journal of Ecology 10, no. 02 (2020): 45–61. http://dx.doi.org/10.4236/oje.2020.102004.

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48

Cichan, Michael A. "Vascular Cambium and Wood Development in Carboniferous Plants. IV. Seed Plants." Botanical Gazette 147, no. 2 (June 1986): 227–35. http://dx.doi.org/10.1086/337588.

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49

Munyenyembe, Hastings. "Economic Assessment of Solar Milling Plants as an Investment Tool: A Case of Katete District-Zambia." TEXILA INTERNATIONAL JOURNAL OF MANAGEMENT 7, no. 2 (August 30, 2021): 84–105. http://dx.doi.org/10.21522/tijmg.2015.07.02.art009.

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The purpose of this study was to assess the economic impact of the solar milling plants to the local people in Katete District, Zambia. The specific objectives were to assess the performance of the solar milling plans, the effect of solar milling plants on mealie meal prices on the local market, the effect of solar milling plants on job creation in the district, and to find out challenges that co-operators are facing in managing the solar milling plants in the district for economic development, suggesting measures to be put in place to see to it that the program was sustainable. The research employed a qualitative research design, and extensive literature reviews were conducted in order to have a broader understanding of the research. The data was collected using the structured questionnaires and interview guide. The main findings of the research were that the hypothesis was rejected because there were no immediate economic benefits of the solar milling plants to the local people of Katete District. Following the results of the research, the solar milling plants were underperforming and underutilized in the district. Solar milling plants had no effect on the price of mealie meals in the district. Solar milling plants had a 40% effect on job creation in the district, and the study concluded that there were no immediate economic benefits brought about by solar milling plants in the district at the time of the study.

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50

Oh, Hyun-Kyung, and Mu-Sup Beon. "Vascular Plants in the Gyeryongsan National Park." Journal of Environmental Science International 18, no. 6 (June 30, 2009): 633–44. http://dx.doi.org/10.5322/jes.2009.18.6.633.

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