Plum

On pome and stone fruit, brown, enlarging rot spots appear, on which concentrically arranged, grey-beige cushions of spores form. Infected fruit rot, dry out and mummify, often remaining on the tree until the next season. In spring the fungus also infects blossoms and short shoots, causing them to die back and killing the branch tips. The disease has two distinct phases. Spring blossom and twig blight (most often Monilinia laxa on stone fruit — sour cherry, sweet cherry, plum, apricot) begins on the blossoms, which turn brown, wilt and dry out without dropping; the infection enters through the stigma and style into the short shoot, girdles it and causes whole shoots to die back, with withered leaves hanging as if scorched — hence the misleading resemblance to frost damage. On stone fruit, infected shoots often exude gum (gummosis) and develop small, cracked bark cankers. The summer-to-autumn brown rot of the fruit (mainly Monilinia fructigena on apple and pear) develops on ripening fruit: the rot spot quickly engulfs the whole fruit, the flesh turns brown and softens, and characteristic, concentrically arranged rings of cream-beige cushions of conidial spores grow out on the surface. In cool conditions (including in storage), the fruit may take the form of hard, black glossy mummies lacking sporulation (so-called black rot). Mummified fruit hanging on the tree and Monilinia cankers on the shoots are the main source of spores in the following season.

Rusty-orange to brown, powdery clusters of spores on the underside of leaves, matched on the upper side by yellow spots. Heavily infected leaves turn yellow and drop prematurely, and the plant weakens. It affects roses and mallows among others, and some rusts have an alternate host (for example pear rust and juniper). The pustules (clusters of summer spores, the so-called uredinia) break through the leaf skin and release an orange-rust powder that rubs off onto the finger - this is the most reliable identifying feature. In high summer they appear mainly on the underside of the blade, along the veins and on the leaf stalks, and in some species also on green shoots and sepals. In late autumn the clusters darken to brownish-black - these are the overwintering spores (telia) by which the fungus survives winter on plant debris. Rusts are highly host-specific: a given rust usually infects only one species or genus of host, which is why the rusts of rose, mallow and marsh mallow, bean, leek and garlic, mint, pelargonium or lawn are different, non-interchangeable fungi. The general symptom - yellowing and premature leaf drop - weakens the plant and limits flowering and yield, though it rarely kills it within a single season.

The disease attacks plum, apricot and peach, along with other species of the genus Prunus. Pale, chlorotic rings, spots and streaks appear on the leaves along the veins, most clearly visible in spring during cool weather. Depressions, discolouration and deformations form on the fruit, and the flesh beneath is often discoloured and gummy with an impaired flavour. Infected fruit frequently drop prematurely, so the crop loses its market and eating value. The leaf symptoms also take the form of vein clearing along the veins and irregular mottling; they are strongest in spring, often fade (become masked) during hot summers and return the following season, which makes diagnosis difficult. The severity of symptoms depends on the strain of the virus and the susceptibility of the cultivar - ranging from almost symptomless forms to severe deformations. On plum fruit, dark, bluish rings and spots as well as depressions are visible; in apricot, characteristic diagnostic rings and spots also appear on the stone (endocarp), which is one of the more reliable identifying features. In peach, colour breaking of the flower petals (paler streaks) is additionally seen. Freshly infected trees can remain symptomless throughout the season, so reliable confirmation is provided only by laboratory testing (the ELISA serological test or molecular RT-PCR).

Sunken, necrotic wounds (cankers) form on the trunk and branches, from which – especially in spring – amber gum oozes (gummosis). The bark over the wounds dies and cracks, and infected buds and short shoots fail to break or die in spring, so whole sections of the crown dry out. Small, brown, watery spots may appear on the leaves and fall out of the blade ('shot-hole'). The disease affects stone-fruit trees – sour cherry, sweet cherry, plum, peach and apricot – and when it girdles a branch it kills it. The cause is two bacterial pathovars — Pseudomonas syringae pv. syringae and pv. morsprunorum — with similar symptoms that cannot be told apart with the naked eye. A characteristic early symptom is the dying of buds and flowers in spring (so-called blossom blast): buds turn brown and fail to open, and individual branches suddenly wilt and dry out, holding their browned leaves for a long time. The gum oozing from the cankers is glassy to amber and appears most abundantly in spring and early summer, after the sap starts to flow; in high summer the ooze usually stops. When the bark is cut at the edge of a canker, the tissue beneath is often watery, rusty-brown, with a sour, fermenting smell (typical of pv. syringae). The leaf spots are at first small, angular, watery and surrounded by a lighter halo; their dead centres crumble away, producing a 'shot-hole' effect. The symptoms are easily confused with frost damage to the bark and with fungal shoot dieback (brown rot) and fungal shot-hole of the leaves (Wilsonomyces carpophilus) — the key then is the season of peak activity and the presence of fungal sporulation. The disease intensifies in cool, wet weather in spring and autumn; in summer, in warmth and drought, the bacterium is least active.

Small (1–3 mm) soft-bodied insects, green, black or pink, feeding in clusters on young shoots and the underside of leaves. They excrete sticky honeydew. The diagnostic feature that distinguishes aphids from other small sucking insects is the pair of siphunculi (tubular projections) at the rear of the abdomen together with a tail-like cauda; a single colony usually holds wingless forms (parthenogenetic females) alongside winged migrants that fly onto new plants in summer. In summer aphids reproduce parthenogenetically and viviparously over many generations, so the population builds up explosively; in autumn many species produce a sexual generation that lays overwintering eggs on the host, and host-alternating species move between a winter host (often a tree or shrub) and a summer host (a herbaceous plant). Feeding symptoms include curling, crinkling and distortion of young leaves, stunted growth, yellowing, and the shedding of buds and fruitlets. Abundant honeydew coats the leaves, and the sooty mould fungus that develops on it forms a black film which limits photosynthesis; the honeydew is fed on by ants, which in return defend the colony against predators. Aphids are also important vectors of plant viruses (mosaics among them), transmitting them from plant to plant even during a brief probing puncture.

A nocturnal moth with a wingspan of 15-20 mm; the forewings are grey-brown with a characteristic coppery, glossy patch at the tip. The caterpillar is whitish to pinkish with a brown head, grows to about 18 mm and tunnels right into the core of an apple or pear (less often quince or walnut). Symptoms: 'maggoty' fruit, entry holes with brown, sawdust-like droppings, and premature fruit drop. The caterpillar has five pairs of abdominal prolegs - the key feature distinguishing it from the larva of the apple sawfly, which has six or more. The codling moth overwinters as a full-grown caterpillar in a dense cocoon hidden in bark crevices, under loose flakes of bark, in the soil at the base of the trunk or in fruit crates; in spring it pupates, and the moths usually emerge from the end of apple blossom (May-June). Flights take place at dusk and at night, when the air temperature rises above about 15C. Females lay eggs singly on the fruit and on leaves nearby; after about one to two weeks the caterpillars hatch and, after a short wandering, bore into the fruit and head for the seed cavity, feeding on the flesh and the seeds. Under Polish conditions there is usually one full generation, and in warmer years and in the south of the country a partial second one whose feeding reaches harvest. Damaged fruit rots, drops prematurely and is unfit for storage.

The caterpillars roll, fold and glue leaves together with a webbing of silk threads, creating shelters in which they feed hidden from view. When disturbed they wriggle violently backwards and drop on threads, which aids their identification; the adults are small moths with a bell-shaped outline of the folded wings. The host plants are fruit trees (apple, pear, plum), ornamental shrubs and roses. Symptoms: the caterpillars chew leaves, flower buds and fruit set and damage the skin of ripening fruit, reducing its value. The name covers many species of the family Tortricidae with a similar way of life - among them the summer fruit tortrix (Adoxophyes orana) and the rose tortrix (Archips rosana). The caterpillars are slender, up to about 1.5-2 cm long, usually light or olive green with a darker head and prothoracic plate, and very active. The moths have a wingspan of about 15-25 mm; at rest they fold the forewings roof-like, giving the characteristic bell-shaped (trapezoidal) outline, and their pattern is greyish-brown with a darker cross-band. The life cycle depends on the species: leaf-rollers overwinter as eggs laid in patches on the bark or as young caterpillars hidden in bark crevices and under bud scales; in spring they bore into the swelling buds, then move onto the leaves and fruit set, and one or two generations develop over the season. A diagnostic feature on pome fruit is the attachment of a leaf to the fruit and the shallow grazing of the skin beneath it, which leaves irregular, corky scars while the flesh deeper inside remains intact. On roses and ornamental shrubs the symptom is rolled young leaflets bound with webbing and hollowed-out buds.

The larvae strongly resemble the caterpillars of butterflies and moths, but have more pairs of abdominal prolegs (six and more) and single ocelli on the sides of the head, by which they can be told apart. They often feed gregariously, skeletonising the leaves or eating them down to the veins, and can strip a gooseberry or currant bush bare within a few days. The host plants are gooseberry, currant, rose, plum and pine. Symptoms: besides the defoliation of leaves, the larvae of fruit-dwelling species (e.g. on plum) bore into the young fruit set and cause it to drop. Adult sawflies are small (a few millimetres) hymenopterans without a distinct 'wasp waist' — the abdomen is broadly joined to the thorax, which distinguishes them from wasps and bees; the females have a saw-like ovipositor (hence the name 'sawflies'), with which they cut into the tissue of a leaf or fruit set and lay their eggs inside it. The larvae are most often green, matching the colour of the leaf, in some species with dark warts or spots; their prolegs lack the grasping crochets that the caterpillars of moths have, and when disturbed the larvae of many species raise the rear end of the body into a characteristic 'S' shape. The most damaging groups are: the gooseberry sawfly (Nematus ribesii) on gooseberry and currant, stripping the bush from the inside out; the slug sawflies (genus Caliroa) on pear, cherry and plum, whose slimy, slug-like larvae graze away the upper skin of the leaf (windowing), so that the leaf turns brown as if scorched; the fruit sawflies of the genus Hoplocampa on plum and apple, tunnelling galleries into the young fruit set and leaving moist, foul-smelling droppings; and the conifer sawflies (Diprion, Neodiprion) on pine, feeding gregariously on the needles. Life cycle: the adults emerge in spring, the larvae feed for several weeks, after which they descend into the soil or leaf litter, where they pupate in a cocoon and overwinter as a larva (prepupa); depending on the species, 1–3 generations develop in a season.

A moth with marked sexual dimorphism: the male has grey-brown, finely banded wings with a span of about 25 mm, whereas the female is practically wingless and flightless and therefore climbs up the trunk in autumn to lay its eggs in the crown. In spring green looper caterpillars with pale lengthwise stripes hatch, moving with the characteristic "looping" gait (arching the rear of the body) and eating the developing buds, young leaves and fruitlets, often webbing them together with threads. It feeds on apple, pear, plum, cherry and many deciduous trees and shrubs. The mature caterpillar reaches about 25 mm in length and is yellow-green with a darker dorsal line and pale stripes along its sides; as a typical looper (Geometridae) it has only two pairs of prolegs at the end of the abdomen, hence its looping gait. The eggs are laid singly near the buds and in bark crevices, where they overwinter, and just before the spring hatch they change colour from greenish to orange-red. The species has one generation a year: the moths fly in late autumn (October-December, which is the origin of the Polish name "przedzimek", meaning before-winter), on cool, frost-free evenings, and the flightless females then climb the trunks. The spring hatch of the caterpillars is closely synchronised with bud burst (usually April); after about 4-6 weeks of feeding the caterpillars lower themselves to the ground on threads and pupate shallowly in the soil, where the pupa spends the summer. The signs of feeding are holed and ragged young leaves, eaten flower and leaf buds, and deformed fruit covered with corky scars that develop from the damaged fruitlets; under heavy pressure the caterpillars can almost strip the crown bare.