Temperatures for seedling emergence of tropical perennial grasses

2017 ◽  
Vol 68 (5) ◽  
pp. 493
Author(s):  
M. K. Egan ◽  
S. P. Boschma ◽  
S. Harden ◽  
C. A. Harris ◽  
C. Edwards

A growth-cabinet study was conducted to determine the optimum temperature range for seedling emergence of seven tropical grasses commonly sown in the frost-prone, summer-dominant rainfall region of inland northern New South Wales. The grasses were Bothriochloa bladhii subsp. glabra (forest bluegrass) cv. Swann, Bothriochloa insculpta (creeping bluegrass) cv. Bisset, Chloris gayana (Rhodes grass) cv. Katambora, Digitaria eriantha (digit grass) cv. Premier, Panicum coloratum var. makarikariense (makarikari grass) cv. Bambatsi, and Megathyrsus maximus (panic) cvv. Gatton and Megamax 059. Six constant temperatures were used, ranging from 10°C to 35°C in 5°C increments. Katambora Rhodes grass was the only grass to emerge at 10°C; seedlings of all grasses emerged at temperatures >10°C. Optimal temperature range for emergence varied between species, falling into three groups: low (Bisset creeping bluegrass 16−22°C); intermediate (Premier digit grass 21−32°C, Swann forest bluegrass 23−31°C, Megamax 059 panic 23−35°C, Gatton panic 24−32°C); and high (Bambatsi makarikari grass 24−35°C, Katambora Rhodes grass 24−35°C). The temperature range at which 50% of optimum emergence occurred was 12−14°C for Katambora Rhodes grass, Bisset creeping blue and Premier digit, and 17−18°C for the panic grasses, Swann forest bluegrass and Bambatsi makarikari grass. These temperatures provide options for sowing earlier in spring or later in summer–autumn and may assist development of sowing time options in new environments and provide insight into competition between species.

2009 ◽  
Vol 60 (10) ◽  
pp. 954 ◽  
Author(s):  
G. M. Lodge ◽  
S. Harden

Two studies were conducted in northern NSW to examine some of the factors affecting the successful emergence of seedlings of five species of tropical perennial grasses [Panicum coloratum var. makarikariense cv. Bambatsi (panic), Digitaria eriantha ssp. eriantha cv. Premier (digit), Chloris gayana cv. Katambora (Rhodes grass), Dichanthium aristatum cv. Floren (bluegrass), and Bothriochloa bladhii ssp. glabra cv. Swann (forest bluegrass)]. The first experiment investigated the effects of depth and time (month) of sowing on tropical perennial grass seedling emergence, while a second series of studies examined the effects of contact of dispersal/sowing units with the soil, particularly over winter, on subsequent seed germination and seedling emergence. No seedling emergence of any species occurred in September 2006 and June–August 2007. From October 2006 to May 2007 there were significant effects (P < 0.001) of species, sowing time, depth, and their interaction on predicted emergence. From December to March, predicted emergence was always lower for surface-sown caryopses compared with those sown at 10 and 25 mm depth, and Bambatsi was the only species that had >50% emergence from a depth of 50 mm. Recovery of intact caryopses from 300 μm nylon mesh bags stored in the soil for 6 and 12 months was low for all species. Similarly, predicted germination of caryopses from field soil surface and buried locations (2007 and 2008) and those from florets and coated seeds (2008) was low, indicating that these species had a poor ability to over-winter in moist soil.


2008 ◽  
Vol 48 (4) ◽  
pp. 553 ◽  
Author(s):  
S. P. Boschma ◽  
G. M. Lodge ◽  
S. Harden

Two adjacent sites (a naturalised pasture and a previously cropped area) with differing potentials for salinity/sodicity and waterlogging near Tamworth, New South Wales were sown with temperate perennial grasses and legumes, temperate annual legumes and tropical perennial grasses to assess their herbage mass and persistence from 2003 to 2006. Plots were either grazed or mown seasonally. Days to flower in the establishment year and seedling regeneration were assessed each year for the annual legumes. In May 2003, salinity levels at soil depths >0.6 m were as high as 8 and 12 dS/m at the naturalised pasture and previously cropped sites, respectively, but generally were >5 and >3 dS/m at a soil depth of 0–0.10 m for these sites in 2004–05. With below average rainfall, no waterlogging was observed at the previously cropped site and only short-term waterlogging of a few days duration occurred at the naturalised pasture site. Under these conditions Puccinellia ciliata cv. Menemen did not establish or perform well, but Thinopyrum ponticum (cvv. Dundas and Tyrrell) was productive and persistent compared with Phalaris aquatica. At both sites, Digitaria eriantha cv. Premier and Chloris gayana cv. Katambora were the best tropical grasses, while the performance of Bothriochloa bladhii subsp. glabra cv. Swann was good at the previously cropped site and Panicum coloratum subsp. makarikariense cv. Bambatsi was best at the naturalised pasture site. At both sites, Medicago sativa had the highest herbage mass and persistence, with cv. Aquarius being superior to cv. Salado after 3 years. Compared with M. sativa, the herbage mass and persistence of Trifolium fragiferum was low. Of the annual legumes, M. polymorpha cv. Scimitar and Melilotus sulcatus had the highest herbage mass.


Soil Research ◽  
2013 ◽  
Vol 51 (8) ◽  
pp. 760 ◽  
Author(s):  
Jonathan Sanderman ◽  
I. R. P. Fillery ◽  
R. Jongepier ◽  
A. Massalsky ◽  
M. M. Roper ◽  
...  

The use of subtropical perennial grasses in temperate grazing systems is increasingly being promoted for production and environmental benefits. This study employed a combination of elemental and stable isotope analyses to explore whether pastures sown to either kikuyu (Pennisetum clandestinum) or a combination of panic (Panicum maximum) and Rhodes grass (Chloris gayana) could increase soil organic carbon (SOC) levels in five regions across southern Australia. Carbon was sequestered under kikuyu at a rate of 0.90 ± 0.25 Mg C ha–1 year–1 along the south coast of Western Australia. Lower but still significant sequestration rates were found for kikuyu in South Australia (0.26 ± 0.13 Mg C ha–1 year–1). No changes in SOC were found for panic–Rhodes grass pasture systems in the northern district of Western Australia. Additionally, we found no changes in SOC when kikuyu-based pastures were established on formerly cropped paddocks in the Namoi Catchment of New South Wales. Stable isotope results corroborated these findings and suggested that, where SOC has accumulated, the gains have been dominated by SOC derived from the perennial vegetation and have been concentrated in the upper 10 cm of soil.


1993 ◽  
Vol 44 (6) ◽  
pp. 1311 ◽  
Author(s):  
GM Lodge ◽  
AJ Schipp

Two experiments examined the effects of sowing time and depth (surface and 10, 25, 50 mm) on emergence of Danthonia richardsonii Cashmore and Danthonia linkii Kunth. Experiment 1 was conducted from January to December 1990 on a loam/sand mixture in boxes. Emergence was highest in both species for seeds sown onto the soil surface in summer and autumn (P < 0.05). Sowing at any depth at any time of the year, or surface sowing in winter and spring, markedly reduced emergence. Experiment 2 was conducted in the field at Tamworth, northern New South Wales from September 1991 to August 1992, on a red brown earth and a black earth. This study confirmed that emergence in both species was highest from surface sown seed. Field emergence was lowest in winter, but in contrast to experiment 1, it was higher in spring, particularly on the black earth. Seedling emergence appeared to be related to mean maximum temperature, decreasing in winter as it declined below 20�C, and increasing in spring when it was greater than 23�C. Differences in seed weight were reflected in emergence of D. richardsonii and D. linkii in experiment 1. Similar emergence was recorded for the loamlsand mixture and sand, indicating that there was little effect of texture. Phalaris aquatica L. cv. Sirosa surface sown in December had lower emergence ( P < 0.05) than both Danthonia spp., but emergence of this larger seeded cultivar was higher at depths of 10 and 25 mm. Laboratory studies to determine reasons for the low emergence of D. richardsonii and D. linkii from depth, indicated that neither had an obligate light requirement for germination. Depth, however, reduced germination (P < 0.05) compared with surface sowing of seed. Seedlings at depth also were observed to have slower rates of shoot and root elongation. In the field, the most successful establishments of D. richardsonii and D. linkii seedlings are likely to occur from surface sowings in April and May. Sowing in spring may also be possible if mean maximum soil temperatures exceed 23�C, and seedlings can establish before the onset of hot, dry conditions in summer.


2003 ◽  
Vol 43 (4) ◽  
pp. 357 ◽  
Author(s):  
W. S. Semple ◽  
I. A. Cole ◽  
T. B. Koen

Thirty perennial grass accessions were evaluated for emergence, growth and persistence at 6 severely salinised seepage scalds on the western slopes of New South Wales. Warm-season accessions were sown or planted in spring 1996 and 1997, and cool-season types in autumn 1996 and 1997. Control species, tall wheat grass (Thinopyrum ponticum) and puccinellia (Puccinellia ciliata) were sown in spring and autumn. Plants were monitored over 2 growing seasons. None of the accessions, including the controls, performed well at all sites. Of the accessions established from seed, tall wheat grass was the most reliable in terms of the number of successful establishments but its growth potential was only achieved at a few sites. Some warm-season species (Panicum coloratum, Chloris gayana and Cynodon dactylon) approached their growth potential at some sites but overall rates of establishment were very low. The performance of puccinellia appeared to be adversely affected by low pH. It was concluded that on severely scalded sites, vegetative propagation of stoloniferous–rhizomatous plants, e.g. Pennisetum clandestinum, Paspalum vaginatum and C. gayana, may be the best option.


2021 ◽  
Author(s):  
Kevin Mganga

&lt;p&gt;Progressive loss of productivity and plant diversity is a major in global rangelands. In African rangelands ecosystems, this process is partly attributed to heavy and uncontrolled grazing by livestock and wildlife, leading to land degradation. Therefore, restoring such degraded rangelands is critical for enhancing ecosystem health and securing the livelihoods of millions of people. Active restoration strategies, e.g. reseeding using indigenous perennial grasses has been identified as a viable ecological solution for restoring degraded African rangelands. Grass species indigenous to African rangelands Cenchrus ciliaris L. (African foxtail grass), Eragrostis superba Peyr. (Maasai love grass), Enteropogon macrostachyus (Hochst. Ex A. Rich.) Monro ex Benth. (Bush rye grass), Chloris roxburghiana Schult. (Horsetail grass) and Chloris gayana Kunth. cv Boma (Rhodes grass) were established in a semi-arid rangeland in Africa under natural conditions to compare their morphoecological characteristics and suitability for use in ecological restoration. Biomass dry matter yields, plant densities, basal cover, seed production, tiller densities and plant height were measured. Chloris gayana cv Boma and E. superba produced significantly higher dry matter biomass yields and seed production than other species. High biomass and seed production demonstrate their suitability to support livestock production and replenish depleted soil seed banks, respectively. Enteropogon macrostachyus and C. ciliaris displayed significantly higher values for plant densities, tiller densities and basal cover, also a component of establishment and ecological restoration success. Chloris roxburghiana ranked lowest in all the measured morphoecological characteristics. This may be a strong indicator of ecological site-specific characteristic of C. roxburghiana. Successful restoration of degraded African semi-arid rangelands using indigenous grass reseeding can best be achieved through careful selection of grasses to take advantage of their specific morphoecological characteristics. This selection should primarily be informed by the intended use of the rangeland.&lt;/p&gt;


2009 ◽  
Vol 60 (6) ◽  
pp. 526 ◽  
Author(s):  
G. M. Lodge ◽  
S. P. Boschma ◽  
S. Harden

Seedlings of three perennial tropical grasses, Chloris gayana cv. Katambora (Rhodes grass), Panicum coloratum var. makarikariense cv. Bambatsi (panic grass), and Digitaria eriantha ssp. eriantha cv. Premier (digit grass), were each grown in replacement series mixtures with seedlings of the annual summer-growing grass weeds Urochloa panicoides (liverseed grass) and Echinochloa colona (awnless barnyard grass). A separate experiment examined the competitiveness of seedlings of the three perennial tropical grasses when two species were sown together. Plants were sown 50 mm apart in boxes at a density of 307 plants/m2. Maximum likelihood estimates were used to derive parameters of a non-linear competition model using the dry weights of perennial and annual grasses. Seedlings of the summer-growing annual liverseed grass competed aggressively with those of the tropical perennial Katambora Rhodes grass. However, Bambatsi panic seedlings were equally competitive with those of awnless barnyard grass, while those in a Premier digit-barnyard grass mixture were inhibited by the presence of each other. In the perennial grass mixtures study, the performance of both Premier digit and Bambatsi panic was adversely affected by the presence of Katambora Rhodes grass.


2004 ◽  
Vol 55 (3) ◽  
pp. 345 ◽  
Author(s):  
G. M. Lodge

A series of seed and seedling studies was undertaken in northern New South Wales for the temperate perennial grasses phalaris (Phalaris aquatica cv. Sirosa and Australian), tall fescue (Festuca arundinacea cv. Demeter), perennial ryegrass (Lolium perenne cv. Kangaroo Valley), and 2 wallaby grasses (Austrodanthonia bipartita syn. Danthonia linkii cv. Bunderra and A. richardsonii syn. D. richardsonii cv. Taranna). Studies were conducted to determine the level of dormancy in freshly harvested seed and the time required to overcome it, effects of alternating daily temperatures on the germination of non-dormant seed, effect of time-of-sowing on seedling emergence (2 studies) and survival, levels of seed production and soil seedbanks, and the effect of litter cover and soil type on the emergence of Sirosa phalaris seedlings.Grass species, time, and their interaction all had a significant effect (P < 0.05) on both dispersal unit and caryopses germination. One month after harvest, germination of caryopses was lower (P < 0.05, 2 and 1%, respectively) for Taranna and Bunderra than for Sirosa (79.5%). In March 1993, germination of the 2 wallaby grasses was also lower (P < 0.05) than that of Sirosa. Dormancy of freshly harvested seeds of Sirosa was mainly associated with the structures surrounding the caryopses (7.7 v. 79.5% mean germination), but for Taranna and Bunderra it was related to physiological dormancy of the caryopses.Germination levels that were not significantly different to the maximum occurred for temperature ranges of 35/30–15/10�C [Sirosa (commercial)], 35/25–15/10�C (Australian phalaris), and 35/30–15/05�C (Kangaroo Valley ryegrass). In contrast, maximum germination of wallaby grasses only occurred for Taranna in the temperature range 25/20–20/10�C, and for Bunderra at 25/15 and 20/15�C.Seedling emergence in the field was episodic, occurring on only 3 occasions from 1993 to 1996. No seedlings of Sirosa phalaris, Demeter tall fescue, or Kangaroo Valley ryegrass were successfully recruited, but Taranna and Bunderra successfully recruited new plants from natural seedfalls. Whereas seed production of the perennial grasses studied was relatively high (~10 000 seed/m2 in 1992), soil seedbank levels were much lower (generally <1000 seeds/m2). These data were used to indicate the likely successful establishment of sown perennial grasses or by regeneration from natural seedfall.


1982 ◽  
Vol 30 (6) ◽  
pp. 611 ◽  
Author(s):  
LA Watt ◽  
RDB Whalley

A range of native and exotic perennial grasses was examined for relationships between seed and seedling features and establishment success on cracking black clay soils of the north-westem slopes of New South Wales. The features examined included the effect of temperature on the speed of germination and cumulative total germination, the effect of the duration of water availability in the seedbed on seedling emergence and the rates of seedling extension. Seedbed temperatures were also monitored during the spring at the Inverell Research Centre. No single seed or seedling feature was consistently associated with establishment success. The two species with the highest rating for establishment, Dichanthium sericeum (R.Br.) A. Camus and Bothriochloa macra (Steud.) S. T. Blake, gave good seedling emergence with only 3 days of seedbed watering, had early and rapid seed germination, germinated well over a wide range of temperatures and had fast root and shoot extension rates. Chloris gayana Kunth, with the lowest establishment rating, had low ratings for all characteristics examined except that it had a moderate speed of germination. Advantageous features at one stage of the sequence from seed to established plant can compensate for weaknesses at another stage, e.g, the fast root and shoot growth rate of Panicum decompositum R. Br. compensates for slow speed of germination, to give a good establishment rating overall.


2013 ◽  
Vol 64 (2) ◽  
pp. 123 ◽  
Author(s):  
E. G. Barrett-Lennard ◽  
Sarita Jane Bennett ◽  
M. Altman

Farmers need methods for assessing the capability of saltland for productive use based on characteristics that are readily measurable at the paddock scale. We conducted experiments on saltland transects with gradients of salinity and depth to watertable at three sites in south-western Australia. Each was planted with five perennial species with at least some salt tolerance: samphire (Tecticornia mellaria K.A.Sheph.), river saltbush (Atriplex amnicola Paul G.Wilson), small leaf bluebush (Maireana brevifolia (R.Br.) Paul G.Wilson), saltwater couch (Paspalum vaginatum Sw.), and Rhodes grass (Chloris gayana Kunth). Survival and growth of species was related to depth to watertable in summer and average subsoil (0.25–0.50 m depth) electrical conductivity of the saturation extract (ECe). It has been hypothesised that plant zonation on land affected by dryland salinity is affected by the level of salinity and waterlogging on sites. While plant survival ≥60% could be associated with particular ranges of depth to watertable and soil salinity, our data suggest that the most important factor affecting survival and growth was the presence of shallow groundwater in summer. The range of depths to watertable in summer associated with ‘good survival’ (≥60%) was 0.7–1.0 m with samphire, 0.7–1.6 m with saltwater couch, 0.8–1.5 m with Rhodes grass, 0.7–2.4 m with river saltbush, and 0.9–2.4 m with small leaf bluebush. The subsoil ECe (95% confidence interval) associated with ‘good survival’ was 5–14 dS/m for Rhodes grass, 6–11 dS/m for small leaf bluebush, 7–11 dS/m for river saltbush, 6–16 dS/m for saltwater couch, and 27–65 dS/m for samphire. Growth of the perennial grasses was strongly affected by the presence of a shallow watertable in summer; the size of saltwater couch and Rhodes grass increased many-fold as watertable depths decreased from ~1.3 to 0.9 m from the soil surface.


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