Lucy Hulmes’s research while affiliated with UK Centre for Ecology & Hydrology and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (21)


Practical methods for the control of tor-grass (Brachypodium pinnatum s.l.) and the restoration of calcareous grassland
  • Article
  • Full-text available

March 2024

·

65 Reads

Journal for Nature Conservation

·

John W Redhead

·

·

[...]

·

Richard F Pywell
Download

The distribution of Geranium pratense in the British Isles. Each dot represents at least one record in a 10 km square of the National Grid. Colour distinguishes native versus alien status, and shade indicates the date range of the most recent record. Figures for Great Britain (GB) and Ireland (IR) indicate total numbers of squares in each category. Source: Stroh, Humphrey, et al. (2023).
Global distribution of Geranium pratense. Reproduced, with modifications, from Hultén and Fries (1986), by permission of Koeltz Scientific Books, Koenigstein, Germany.
Typical roadside verge habitat conforming to MG1 Arrhenatherum elatius grassland. Near Swayfield, Lincolnshire, UK.
Pollen grain of Geranium pratense. Left: general view (scale 50 μm); right: sculpture of the exine surface (scale 10 μm). Adapted from Troshkina (2018).
Close up of the flower showing the arrangement of the stamens, anthers, and a non‐receptive stigma.

+3

Biological Flora of Britain and Ireland: Geranium pratense

October 2023

·

157 Reads

·

1 Citation

This account presents information on all aspects of the biology of Geranium pratense L. (Meadow Crane's‐Bill). The main topics are presented within the standard framework of the Biological Flora of Britain and Ireland : distribution, habitat, communities, responses to biotic factors, responses to environment, structure and physiology, phenology, floral and seed characters, herbivores and disease, history and conservation. Geranium pratense is a perennial gynodioecious forb of neutral grassland. In Britain and Ireland, it is particularly abundant on roadside verges, railway embankments, the margins of watercourses and woodland rides. It is generally intolerant of grazing and is absent or scarce in livestock‐grazed grassland. Geranium pratense is widespread in England, Wales and Scotland but is scarce in Ireland. It has an extensive native range in Europe and Asia, extending eastwards to Russia, north‐western China and Mongolia. It has been widely introduced to new sites within its native range and has been introduced to Canada, the USA and New Zealand. Geranium pratense usually occurs on free‐draining soils but also infrequently where drainage is impeded. The soils are often nutrient‐rich and weakly acidic to weakly alkaline. The underlying geology is usually non‐acidic sedimentary rocks or superficial deposits. Geranium pratense is protandrous and is pollinated by various insects of the orders Hymenoptera, Diptera and Lepidoptera, particularly bumblebees, solitary bees, hoverflies and butterflies. Eleven species of phytophagous insect have been recorded on G. pratense in Britain and Ireland. Geranium pratense has little or no capacity for vegetative spread. Primary seed dispersal is ballistic and seeds may be flung over distances of up to several metres. The species has a transient seed bank, that is germination typically takes place in the winter and spring after seed production, after the physically dormant seeds have become permeable. Seedling establishment is higher in vegetation‐free gaps than in undisturbed grassland vegetation. There has been no significant change in its distribution between the late 1950s and 2019, although since 2000, it has expanded its range, mainly via introductions, in northern and western Scotland, west Wales and in Ireland. Alien sites have increased markedly since the 1960s due to introductions from wildflower seed sowing and spread from gardens.


The potential to increase grassland soil C stocks by extending reseeding intervals is dependent on soil texture and depth

February 2023

·

42 Reads

·

12 Citations

Journal of Environmental Management

Grasslands account for ∼30% of global terrestrial carbon (C), of which most is stored in soils and provide important ecosystem services including livestock and forage production. Reseeding of temporary grasslands on a 5-year cycle is a common management practice to rejuvenate sward productivity and reduce soil compaction, but is physically disruptive and may reduce soil organic carbon (SOC) stocks. However, research to date is limited, which impacts on the ability to optimise grassland management for climate change mitigation. To determine whether extending the time interval up to 20 years between grassland reseeding can increase stable SOC stocks, a soil survey was conducted across three UK grassland chrono-sequences comprising 24 fields on contrasting soil types. We found that grassland SOC stocks (39.8-114.8 Mg C ha-1) were higher than co-located fields in arable rotations (29.3-83.2 Mg C ha-1) and the relationship with grassland age followed a curvilinear relationship with rapid SOC stock accumulation in the year following reseeding (2.69-18.3 Mg C ha-1 yr-1) followed by progressively slower SOC accumulation up to 20 years. Contrary to expectation, all grasslands had similar soil bulk densities and sward composition questioning the need for traditional 5-year reseeding cycles. Fractionation of soils into stable mineral associated fractions revealed that coarse textured grassland topsoils (0-15 cm) were near-saturated in C irrespective of grassland age whilst loam soils reached saturation ∼10 years after reseeding. Fine-textured topsoils and subsoils (15-30 cm) of all textures were under saturated and thus appear to hold the most potential to accrue additional stable C. However, the lack of a relationship between C saturation deficit and grassland age in subsoils suggests that more innovative management to promote SOC redistribution to depth, such as a switch to diverse leys or full inversion tillage may be required to maximise subsoil SOC stocks. Taken together our findings suggest that extending the time between grassland reseeding could temporarily increase SOC stocks without compromising sward composition or soil structure. However, detailed monitoring of the trade-offs with grassland productivity are required. Fine textured soils and subsoils (15-30 cm) have the greatest potential to accrue additional stable C due to under saturation of fine mineral pools.


Establishment and management of wildflower areas for insect pollinators in commercial orchards

November 2021

·

152 Reads

·

21 Citations

Basic and Applied Ecology

Sown wildflower areas are increasingly recommended as an agri-environmental intervention measure, but evidence for their success is limited to particular insect groups or hampered by the challenges of establishing seed mixes and maintaining flower abundance over time. We conducted a replicated experiment to establish wildflower areas to support insect pollinators in apple orchards. Over three years, and across 23 commercial UK orchards with and without sown wildflowers, we conducted 828 transect surveys across various non-crop habitats. We found that the abundance of flower-visiting solitary bees, bumblebees, honeybees, and beetles was increased in sown wildflower areas, compared with existing non-crop habitats in control orchards, from the second year following floral establishment. Abundance of hoverflies and other non-syrphid flies was increased in wildflower areas from the first year. Beyond the effect of wildflower areas, solitary bee abundance was also positively related to levels of floral cover in other local habitats within orchards, but neither local nor wider landscape-scale context affected abundance of other studied insect taxa within study orchards. There was a change in plant community composition on the sown wildflower areas between years, and in patterns of flowering within and between years, showing a succession from unsown weedy species towards a dominance of sown species over time. We discuss how the successful establishment of sown wildflower areas and delivery of benefits for different insect taxa relies on appropriate and reactive management practices as a key component of any such agri-environment scheme.


Mapping distributions of Alopecurus myosuroides. (a) The distribution of A. myosuroides in BSBI atlases and new sites found in this study. (b) The sites surveyed in this study.
Modelled density of Alopecurus myosuroides in (a) 2015, (b) 2016, (c) 2017 and (d) 2018. The maps show generalized additive models to the survey data, describing geographical variation through a thin plate regression spline (see text for details). The standard errors (units of density) of the fitted values are shown in (e)–(h).
Map of modelled density of Alopecurus myosuroides. The model includes soil type and rainfall (Table 2) as well as a smooth term (thin plate regression spline, see text for details).
Risk modelling of Alopecurus myosuroides: map of modelled density of the whole of England and Wales. The smooth term has been removed so the map shows variation in density attributable to soil and rainfall, that is, relative suitability in terms of edaphic conditions only.
Comparison of predicted densities based on model predictions based on the national field‐scale density assessments (Fig. 4) with occupancy recorded in the atlas data (Fig. 1(a)). In each case we have compared the predictions from the model with the records of presence and absence from one of the atlases: (a) 1960s atlas (Wilcoxon test rrb = 0.44, P < 0.0001); (b) 2000 atlas (Wilcoxon test rrb = 0.52, P < 0.0001); (c) 2020 atlas (Wilcoxon test rrb = 0.62, P < 0.0001); (d) 2020 atlas supplemented with the data collected in this study (Wilcoxon test rrb = 0.64, P < 0.00001). Note the y axis presents normalised density, relative to minimum and maximum predicted densities, hence is on a 0–1 scale.
Characterizing the environmental drivers of the abundance and distribution of Alopecurus myosuroides on a national scale

February 2021

·

75 Reads

·

10 Citations

BACKGROUND Arable weeds threaten farming and food production, impacting on productivity. Large‐scale data on weed populations are typically lacking, and changes are frequently undocumented until they reach problem levels. Managing the future spread of weeds requires that we understand the factors that influence current densities and distributions. In doing so, one of the challenges is to measure populations at a large enough scale to be able to accurately measure changes in densities and distributions. Here we analyse the density and distribution of a major weed (Alopecurus myosuroides) on a large scale. Our objectives were to (i) develop a methodology for rapid measurement of occurrence and abundance, (ii) test hypotheses about the roles of soils and climate variation in determining densities, and (iii) use this information to identify areas in which occurrence could increase in the future. RESULTS Populations were mapped through England over 4 years in 4631 locations. We also analysed UK atlas data published over the past 50 years. Densities of populations show significant interannual variability, but historical data show that the species has spread. We find significant impacts of soil and rainfall on densities, which increase with the proportion of heavy soils, but decrease with increasing rainfall. Compared with independent atlas data we found that our statistical models provide good predictions of large‐scale occupancy and we provide maps of current and potential densities. CONCLUSION Models of spread highlight the localised nature of colonisation, and this emphasises the need for management to limit dispersal. Comparisons of current, historical and potential distributions suggest sizeable habitable areas in which increases in abundance are still possible. © 2021 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.


Green hay transfer for grassland restoration: species capture and establishment

August 2020

·

189 Reads

·

24 Citations

Restoration Ecology

Green hay transfer from species‐rich donor sites is now commonly used in Europe to restore species‐rich semi‐natural grassland, both on ex‐arable land and on formerly intensive species‐poor grassland. However, species transfer rates are usually well below 100%, and due to lack of further colonization by additional target species, continued progress towards the target plant community after initial restoration is often very slow. We used data from a restoration experiment aiming to re‐establish species‐rich grazed meadows of the MG5 grassland type according to the British National Vegetation Classification to investigate relationships between species abundance at a donor site, species capture by green hay and its seed content, and success of species establishment on experimental plots in formerly intensively managed species‐poor grassland undergoing restoration. Our results show that species with higher abundance at the donor site got more likely captured as seed in the transferred green hay, and more likely established after hay application at the recipient site. Species with low abundance at the donor site and simultaneously possessing specific germination requirements preventing immediate establishment after hay transfer were particularly unlikely to get established after hay transfer. These findings can provide guidance for additional measures aimed at ensuring establishment of a wider range of target species. Such measures could include the targeted sowing of species in addition to green hay application, and management of restored grassland swards to extend or re‐open an initial window of opportunity for the establishment of green hay species that might not be germinable immediately after hay transfer. This article is protected by copyright. All rights reserved.


Figure 1. Soil characteristics in experimental plot areas of low and high flood risk. Bar charts show back-transformed mean values, and error bars indicate AE SE (n = 12). For comparison, the range of values for these parameters as measured in local arable fields is indicated by orange bands, and the range of values as measured at the green hay donor site is indicated by green bands, representing potential starting points and a potential endpoint of grassland restoration, respectively (in each case n = 4).
Figure 2. Restoration progress from 2014 to 2017 for areas of low flood risk and areas of high flood risk in the three experimental treatments. Parameters include (A) Bray-Curtis similarity to the vegetation at the hay donor site, (B) TABLEFIT goodness-of-fit to MG5 grassland (Hill 2015), (C) total cover of MG5 positive indicator species (Robertson & Jefferson 2000), (D) MG5 positive indicator species richness per m 2 and (E) total species richness per m 2 . Back-transformed means AE SE are shown (n = 4).
Green‐hay application and diverse‐seeding approaches to restoring grazed lowland meadows: progress after four years and effects of a flood risk gradient

April 2020

·

60 Reads

·

8 Citations

Restoration Ecology

The two most common approaches to target species introduction in European meadow restoration are green‐hay transfer from species‐rich donor sites and the use of diverse seed mixtures reflecting the chosen target community. The potential of both approaches to restore species‐rich grassland has been variously reviewed, but very few studies have experimentally compared them at one and the same site. Moreover, studies involving one or both approaches have rarely taken into account environmental gradients at a site, and measured the impacts of such gradients on restoration outcomes. Such gradients do e.g. exist during grassland restoration on former arable land in river floodplains, where gradients in the occurrence of flooding, and in associated edaphic characteristics such as nutrient availability, might affect restoration outcomes. Using a randomised complete block experimental design, based on five different indicators of restoration progress, we compared the usefulness of green‐hay application and diverse‐seeding to restore species‐rich grazed meadows of the MG5 grassland type according to the British National Vegetation Classification, and also investigated how restoration outcomes differed after four years between areas within experimental plots characterized by high flood risk, and areas characterized by low flood risk. Overall, both restoration approaches yielded similar results over the course of the experiment, whereas high flood risk levels and associated edaphic factors such as high availability of phosphorus negatively affected restoration progress particularly in terms of floristic similarity to restoration targets. These results highlight the need to take into account environmental gradients during meadow restoration.



Fig. 1. Location of the 33 experimental sites in the United Kingdom, Hungary, and Germany. See fig. S2 for a diagrammatic representation of the experimental setup. 
Fig. 2. Summary effect sizes for the response of honey bees and wild bees to the neonicotinoid seed treatments. An effect size represents the difference between the mean population response for a given seed treatment and the control within a country, with this difference divided by the pooled standard deviation, where asterisk (*) indicates a significant difference between the control and seed treatment [either TMX (thiamethoxam) or CTD (clothianidin)] determined from the predicted marginal means of the model "y ~ seed treatment × country + block/country. " Dagger ( †) indicates where U.K. colony survival was too low for a formal analysis. Note that effect sizes differ between countries. 
Fig. 3. Wild bee reproductive success in response to neonicotinoid nest residues. Separate graphs are shown for the response of B. terrestris queen production and O. bicornis reproductive cell production to neonicotinoid residues found in nests. The significance of these relationships is based on a likelihood ratio test comparison of H0: "y ~ country" and H1: "y ~ neonicotinoid + country." Neonicotinoid residues are based on summed concentrations of clothianidin, thiamethoxam, and imidacloprid. 
Country-specific effects of neonicotinoid pesticides on honey bees and wild bees

June 2017

·

2,852 Reads

·

610 Citations

Science

Damage confirmed Early studies of the impacts of neonicotinoid insecticides on insect pollinators indicated considerable harm. However, lingering criticism was that the studies did not represent field-realistic levels of the chemicals or prevailing environmental conditions. Two studies, conducted on different crops and on two continents, now substantiate that neonicotinoids diminish bee health (see the Perspective by Kerr). Tsvetkov et al. find that bees near corn crops are exposed to neonicotinoids for 3 to 4 months via nontarget pollen, resulting in decreased survival and immune responses, especially when coexposed to a commonly used agrochemical fungicide. Woodcock et al. , in a multicounty experiment on rapeseed in Europe, find that neonicotinoid exposure from several nontarget sources reduces overwintering success and colony reproduction in both honeybees and wild bees. These field results confirm that neonicotinoids negatively affect pollinator health under realistic agricultural conditions. Science , this issue p. 1395 , p. 1393 ; see also p. 1331


Figure 1: Summed percent cover of a, b all non-crop species, c, d species of faunal value, e, f rare and declining arable species, and g, h undesirable weeds. Left panel winter wheat experiment; right panel spring barley experiment. Back-transformed mean ± SE shown for different combinations of cereal sowing at standard (‘1/1’) versus one-quarter of standard (‘1/4’) densities and N application at typical rates (‘+N’) versus no N (‘−N’), and also for an uncropped cultivated control treatment (‘Control’). Asterisks indicate significant pairwise differences between individual cereal-sown treatments and the uncropped control (Dunnett tests: * 0.01 ≤ P < 0.05; ** 0.001 ≤ P < 0.01 *** P < 0.001)
Figure 2: Species richness per 1.25 m2 of a, b all non-crop species, c, d species of faunal value, and e, f rare and declining arable species. Mean ± SE shown. See also caption and legend of
Figure 3: Establishment of sown rare arable species in terms of numbers of plants per m2 of a, b all sown species pooled together and c, dK. spuria. Mean ± SE shown. See also caption and legend of
Figure 4: Vegetation structural parameters, including a, b percentage bare ground, c, d cereal tiller density, as number of tillers per m2, and e, f vegetation height in metres. Mean ± SE shown. See also caption and legend of
Cereal density and N-fertiliser effects on the flora and biodiversity value of arable headlands

January 2017

·

77 Reads

·

15 Citations

Biodiversity and Conservation

Modern intensive farming caused pronounced changes to the European arable flora. Many species adapted to less intensive traditional farming declined severely, as did the potential of unsown arable vegetation to support higher trophic levels. To reverse these trends, various agri-environment measures were introduced. One such measure is to manage cereal headlands as conservation headlands, involving strict restrictions on pesticide and fertiliser use. An additional modification to management which could reduce crop competition and thus deliver benefits to arable plants is cereal sowing at reduced rates. However, little is known about its benefits to rare and declining arable plants, or to species of value to higher trophic levels, and whether it can be implemented without concomitant increase in undesirable weeds. We set up identical two-factorial experiments in winter wheat and spring barley, combining a nitrogen fertiliser versus no fertiliser treatment with cereal sowing at economic rates versus sowing at rates reduced by 75 %, with added sowing of a mixture of rare arable species. Both experiments also included an uncropped but cultivated control equivalent to another agri-environment measure. Our results show that reduced cereal sowing in conservation headlands can benefit rare and declining species, as well as arable plant diversity, without necessarily resulting in a concomitant increase in undesirable weeds. While such benefits tended to be larger in uncropped cultivated controls, conservation headlands have the advantage of not requiring land being taken out of production. Moreover, as shown in this study, their benefits to arable plants can be maximised by reduced sowing.


Citations (17)


... Cumulative sum of litter-C respired (a) and total SOM derived (primed) C (b) over the course of the 126-day incubation. CO 2 sampling was conducted daily from days 0-10 and then on days 13,15,17,20,24,28,31,34,38,41,45,49,56,63,70,77,84,91,98,105,112, 119 and 126. The cumulative sum of litter-C respired is presented as a percentage of the C added as litter whilst primed C represents pre-existing C respired from litter addition treatments in excess of C respired from no litter control microcosms. ...

Reference:

Microbial and mineral interactions decouple litter quality from soil organic matter formation
The potential to increase grassland soil C stocks by extending reseeding intervals is dependent on soil texture and depth
  • Citing Article
  • February 2023

Journal of Environmental Management

... al. 2015;Carvell et al. 2022). The hierarchical clustering dendrogram revealed that treated elds near diverse bunds shared a more similar species composition than the treated elds near to less diverse and barren bunds. ...

Establishment and management of wildflower areas for insect pollinators in commercial orchards
  • Citing Article
  • November 2021

Basic and Applied Ecology

... Finally, the risk to national wheat production is negligible. In areas where black-grass resistance is not yet a problem, it would therefore be in land managers' interests to act pre-emptively and diversify rotations before resistance arises, particularly as there are sizeable areas in which increases in black-grass abundance are still possible in the UK 35 . These LD-LR MIT rotations should also be implemented with the introduction of any new herbicidal mode of action to which there is currently no resistance (e.g., Bixlozone, due this year). ...

Characterizing the environmental drivers of the abundance and distribution of Alopecurus myosuroides on a national scale

... Since unfertilized riparian buffer strips may in any case produce forage with lower quality, which is best fed to heifers and non-lactating cows, it might be advisable for the farmer to spare buffer strips from the intensive mowing cycle of the grassland and to harvest the buffer strip hay separately only once or twice in summer. Results from various restoration trials demonstrate that substantial increases in phytodiversity can be achieved with this procedure even in former intensive grassland (Wagner et al. 2021;Valkó et al. 2022). If a variable part of the buffer strips is left uncut in autumn, the benefit for plants, vertebrates and invertebrates will be even greater. ...

Green hay transfer for grassland restoration: species capture and establishment

Restoration Ecology

... Consistent with studies showing a delayed establishment of target species, in particular specialists (Wagner et al. 2021;Valk o et al. 2022), the negative effect of the hay input was rather transient. Our results provide evidence for the transfer of a Target species, Lathyrus nissolia, within the hay. ...

Green‐hay application and diverse‐seeding approaches to restoring grazed lowland meadows: progress after four years and effects of a flood risk gradient

Restoration Ecology

... Pesticide seed treatments take advantage of the systemic nature of the chemicals. The coatings are designed to be absorbed through a plant's roots as it grows, making all of the plant's tissues including the pollen and nectar poisonous to target pests and beneficial insects such as bees, butterflies, and other pollinators [58][59][60]. Though the use of seed treatments is not tracked, one can estimate it by examining U.S. Geological Survey (USGS) Pesticide Use annual reports, which beginning in 2015 discontinued reporting on the seed treatment applications [61]. ...

Country-specific effects of neonicotinoid pesticides on honey bees and wild bees

Science

... Although FE Grass Margins showed the most promise in providing the greatest number of key plant species for insect pollinators, as the areas aged, only L. vulgare remained in high abundance. Therefore, we suggest these areas experience some level of disturbance, either through replacement, scarification, or herbicide application after ten years to encourage higher floral diversity (Potts et al., 2007). Additionally, Pollen & Nectar Strips only had a substantial presence of Trifolium spp., species strongly favoured by bumblebees and honeybees, but little else (Wood et al., 2015). ...

Experiment 2 - Management of the non-cropped margin structure to maximise biodiversity.
  • Citing Chapter
  • June 2007

... (e.g. tillage, fertilizer inputs, weed control) have indeed selected for specific plant strategies (Storkey et al., 2005;Weiner et al., 2010;Bagavathiannan & Norsworthy, 2012;Fried et al., 2012;Gaba et al., 2014;Pinke & Gunton, 2014;Wagner et al., 2017) resulting in a narrower functional niche of the most tolerant weeds (i.e. specialist weeds mostly occurring in agricultural fields) while generalist weeds occurring in different types of habitats (among which croplands) are generally functionally similar to grassland species (Bourgeois et al, 2019). ...

Cereal density and N-fertiliser effects on the flora and biodiversity value of arable headlands

Biodiversity and Conservation

... Some winter crops for farmland birds support a higher diversity of bird species than conventional crops , Field et al. 2011). However, others do not actually succeed in providing a source of food throughout the winter (Siriwardena et al. 2008, Hinsley et al. 2010, Bright et al. 2014). This can be addressed by supplementing seed-bearing crops with extra food in late winter according to Broughton et al. (2020). ...

Performance and effectiveness of winter bird food patches established under environmental stewardship: Results from the hillesden experiment